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7/30/2023

Environmental Pollution Control


ETZC362/PEZC411

Prof. Krishna C. Etika


BITS Pilani Associate Professor
Pilani Campus Department of Chemical Engineering
B.I.T.S-Pilani, Pilani Campus

Lecture-1
30-07-2023
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Pilani Campus

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Introduction
BITS Pilani
Pilani Campus

ETZC362/PEZC411 Environmental Pollution Control

Handout
Topics Lecture No
Impact of Man on the Environment: An Overview 1
Air Pollution: Sources and Effects 2
Meteorological Aspects of Air Pollutant Dispersion 3-4
Air Pollution Sampling and Measurement 5
Air Pollution Control Methods & Equipment 6-7
Review 8
Water Pollutants 9
Wastewater Sampling and Analysis 10
Waste Water Treatment 11-13
Hazardous Waste Management 14
Noise Pollution 15
Review 16

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Handout
Evaluation Component Name Type (Open Weight Duration Day, Date,
(Quiz, Lab, Project, Mid- book, Session, Time
term exam, End semester Closed
exam, etc.) book,
Online, etc.)
EC - 1 Quiz I September 10,
Online 5% 10 min
2023
Quiz II October 14,
Online 10% 20 min
2023
Quiz III November 12,
Online 10% 20 min
2023
EC - 2 Mid-Semester Test Sunday,
Closed
35% 2 hours 24/09/2023
Book
(Evening)
EC - 3 Comprehensive Exam Sunday,
Open Book 40% 2 ½ hours 26/11/2023
(Evening)

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Contact List of Topic Sub-Topics Referenc


Hour Title e
 The Biosphere T1- Ch.1
 The Hydrologic Cycle
 The Nutrient Cycles- Carbon,
Impact of
Nitrogen, Phosphorus,
Man on the
1-2 sulphur
Environment:
 Consequences of Population
An Overview
Growth-Exponential Growth
 Self-Study: Environment
Trends
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Introduction

What is an Environment?

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Introduction
The term environment is a broad term with many different
definitions, and the term is used differently by different
people. Thus it makes it difficult to define exactly what the
environment is??

The natural world or physical surroundings in general, either as


a whole or within a particular geographical area, esp. as
affected by human activity.

"The area surrounding a place or thing; the environs,


surroundings, or physical context."

Are Human’s Part of Environment???? 8


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Reality Check! https://aqli.epic.uchicago.edu/country-


spotlight/india/#:~:text=Lucknow%2C%20the%20capital%20of%20India's,Delhi%20is%20also%20highly
%20polluted.

All of India’s 1.4 billion


people live in areas where
the annual average
particulate pollution level
exceeds the WHO guideline.
Ninety-four percent live in
areas where it exceeds
India’s own air quality
standard.

“India is today the world’s second most polluted country. Air pollution shortens the average
Indian life expectancy by 6.3 years, relative to what it would be if the World Health Organization
(WHO) guideline was met; 3.4 years relative to what it would be if pollution were reduced to
meet the country’s own national standard. Some areas of India fare much worse than average,
with 30
airJuly
pollution
2023
shortening lives by more than 10 years in Delhi and its surrounding region.”
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Reality Check!

Arsenic has been found in water in parts of 209 districts in


25 states and Union territories, while uranium has been
found in parts of 152 districts across 18 states.

Also, there are 14,079 iron-affected, 671 fluoride-affected,


814 arsenic-affected, 9,930 salinity-affected, 517 nitrate-
affected and 111 heavy metal-affected habitations in the
country.

Read more at:https://economictimes.indiatimes.com/news/india/arsenic-found-in-ground-


water-in-parts-of-209-districts-uranium-in-parts-of-152-districts-
govt/articleshow/93279825.cms

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Reality Check!
“Air and noise pollution should now be considered as
one of the major factors causing cardiac irregularities. As
cardiologists, we are used to thinking about many
traditional risk factors such as smoking, hypertension, or
diabetes. This study and others suggest that we should
start considering additional risks.”

Annual Frontier Report, 2022’


published by the United Nations Thirteen cities from South Asia feature in the
Environment Program. list. Five of them from India: Kolkata at 89 dB,
Asansol (89 dB), Jaipur (84 dB), and Delhi (83
The report ranks 61 cities around the world dB)
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Reality Check!

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Introduction

• Systematic pollution of our environment is one of the


biggest hazards faced by humanity today
• Task of preserving the purity of environment is of utmost
significance
• Two most pressing demands are (1) protection of
environment (2) efficient use of natural resources

• There is need of technical manpower who could develop


and implement effective means for protecting the
environment

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Environmental engineering

• The application of science and engineering principles,


under constraint, to the protection and enhancement of
the quality of the environment and to the enhancement
and protection of public health and welfare

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Impact of Man on the


Environment: An Overview
The Biosphere

The Hydrologic Cycle

The Nutrient Cycles- Carbon,Nitrogen, Phosphorus,


sulphur

Consequences of Population Growth-Exponential Growth

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BIOSPHERE

• The Environment which Supports Life and sustains


various human activities is known as biosphere
• Extends to about 20 km from the bottom of ocean to the
highest point in the atmosphere where life can be
sustained without protective devices
• Essentials for Life: Light, Heat, water, food and habitats
are supplied by the biosphere
• Biosphere is divided into smaller units or ecosystems
• All ecosystems can be divided into two parts
• Biotic (living) and abiotic (non living) components

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BIOSPHERE – Variety of
known living species

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BIOSPHERE

• The biotic category is subdivided into three functional


groups
• Producers (autotropic-self nourishing): Green Plants and algae
• Consumers (heterotrophic-other nourishing): animal life : fish, insects, birds, they
depend on consumption of Producers
• Decomposers (heterotrophic organisms): bacteria, algae that breaks down
complex compounds from waste materials

• Example : Operating ecosystem: Pond


• Abiotic substances – water, nutrients, oxygen and CO2
• Producers: large rooted plants and free floating minute plants (store energy and
liberate O2)
• Primary Consumers: Benthos or bottom forms and zooplankton with little or no
swimming ability. Phytoplankton are consumed by zooplankton which in turn
eaten by large aquatic life such as fish.

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BIOSPHERE – Pond Example


(contd)

• Other consumers are insects, frogs and man


• All these forms produce organic waste and dead organisms.
• The decomposers bacteria and fungi utilize organic carbon and
generate CO2 Used By Algae
• The availability of the Nutrients carbon, phosphorus and nitrogen is
sufficiently small so as to limit the production of algae and maintain
dynamic equilibrium.
• The chemical elements circulate between the organisms and the
environment through pathways comprising of the natural cycles
• 1) hydrologic cycle
• 2) Biochemical cycles
• Carbon
• Phosphorus
• Nitrogen and sulphur
• These cycles operate in a balanced state with little variation thereby
contributing to the stability of atmosphere materials

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BIOSPHERE – Pond Example


(contd)

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Hydrologic Cycle
• Natural cycle : More than 97% of water in biosphere is in oceans, the remaining
3% is found in continents and atmosphere
• More than 70% of this is in glaciers and icecaps
• Water on which human depend such as lakes, streams and ground water
accounts for less than 1% of total supply
• The hydrologic cycle of the biosphere depends on the reciprocity of evaporation
and precipitation. Liquid water on earth goes to the atmosphere as vapor by
evaporation and transpiration of the plants. The vapor is returned to Earth as
rain or snow over the oceans and oceans lose more water by evaporation than
they gain by precipitation. The difference is made up by runoff and seepage
from the continents, over which there is more precipitation than evaporation.
Continents lose more than 50% of the precipitation through evaporation and
remainder is stored in lakes, rivers or ground water which is later discharged
into oceans.
• Each year 4,23000 km3 water is evaporated, same quantity precipitated
• Amount of water temporarily stored & later discharged is 37000 km3
• This water is available for human use
• Minor modification by diverting or regulating the runoff and storage

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BIOSPHERE – Pond Example


(diagram)

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Nutrients Cycle (carbon cycle)

• Dynamic equilibrium of formation, transformation and


decomposition of carbon compounds
• The producers through photosynthesis reduce carbon dioxide
from the atmosphere to organic carbon
• This then passes through consumers and decomposers,
which reenters the atmosphere through respiration and
decomposition
• Even though the amount of CO2 in the atmosphere is of major
concern, the atmospheric reservoir for carbon is the smallest
and oceans hold the largest amount as a vast “sink” for CO2
• Typical reservoirs of carbon
• Oceans -40000 (billion tonnnes)
• Fossil fuels, rocks and minerals -5000 to 10000
• Soil- 2000
• Atmosphere- 750

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Nutrients Cycle (carbon cycle)

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Nutrients Cycle (carbon cycle)

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Nutrients Cycle (carbon cycle)


• Oceans store 50 times as much as the atmosphere
• Human activity releases roughly 7 billion tons of carbon
• Out of 7 billion tones 3 billion tons accumulate in the atmosphere
and the rest is taken up by ocean and terrestrial plants
• The exact mechanism by which the sea water interacts with the
air above it to remove CO2 is not clearly understood but the
oceanic reservoir tends to regulate the CO2 concentration.
• Even though the ~3 billion tons added to the atmosphere each
year is tiny fraction of the total held by the atmosphere, it
assumes significance because the natural processes and the
environment maintain dynamic equilibrium whereas human
activity put burden.
• Any global event that alter the exchange of CO2 between the
atmosphere and the ocean can significantly affect the
concentration of CO2 in the atmosphere
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Nutrients Cycle (carbon cycle)

• Apart from daily consumption and production of carbon, earth


has significant reserves (limestone, fossil fuels (coal and
petroleum)
• Due of combustion some of bound carbon returns to the
atmosphere as carbon dioxide or carbonic acid
• Plants grow faster in CO2 enriched atmosphere but is offset
by the denudation of forests, as a result detectable increase
of CO2 has been Observed
• Atmospheric CO2 concentration stable at 280 +/- 10 ppm till
onset of industrial revolution
• By 1959 CO2 concentration stable at 316 ppm, 1998: 367
(17% increase) and has reached 380 ppm by 2004 . Human
activities has disturbed the carbon cycle

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Nutrients Cycle ( Nitrogen


cycle)
• Nitrogen is gaseous form – 79% in atmosphere
• Cannot be used directly by most forms of life
• It must be fixed before utilization by plants and animals
• By fixation, nitrogen is converted to nitrates and ammonia
• Physicochemical and biological means
• Biological ( free living bacteria Azetobacter , clostridium or leguminuous
plants like Rhizaobium and blue green algae)
• They are key for atmospheric movement nitrogen
• The nitrates are assimilated to form amino acids , urea and other organic
residues in the producer, consumer and decomposer cycle.
• Amino acids and urea---converted to ammonia through “ammonification”
• To complete the cycle the denitrifying bacteria convert the ammonia into
nitrates and nitrates and then back to nitrogen
• Thus Total amount of nitrogen= total amount required to the atmosphere
as gas
• Human’s interference with the natural cycle by industrially fixing
nitrogen(fertilizers)

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Nutrients Cycle ( Nitrogen


cycle)

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Nutrients Cycle ( Phosphorus


cycle)
• Phosphorus plays important role in the growth of living tissue
• Metabolic process of energy transfer does not form gaseous
compounds at normal T, P
• Reservoirs in land are, rock and natural phosphate deposits
• Much of it is fixed in soil or absorbed on to soil particles
• Some of it lost to water bodies such as lake and streams and
eventually ends up in the ocean where phosphorus is
deposited partly in shallow sediments and partly in deep zone
• Land plants take up inorganic phosphate salts from soil and
convert them to adenosine triphosphate (ATP) and adenosine
diphosphate (ADP)

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Nutrients Cycle ( Phosphorus


cycle)
• ATP and ADP are utilized by plants as energy carriers for their metabolic
reactions
• Organic phosphates are transferred to consumers and decomposers and
subsequently available as inorganic phosphates for recycling via bacterial
decomposition
• The inorganic phosphates that are leached from the land into the fresh water
systems are taken up rather rapidly by phytoplankton and are converted to
organophosphates. This phosphorus is ingested by zooplankton which are
consumed by other organisms . After their death the phosphates are released
into water by bacterial decompositon.
• Ocean cycle-Phosphates from unlighted depths to the photosynthetic zone
where it goes through phytoplankton, zooplankton and animal stages.
• Zooplankton-Excreate : Of that half is in inorganic form and rest organic
• Some of the phosphorus return to the land through fish harvesting. More
phosphorus is lost than it it is being added. Some concern there-Growth
determining nutrient
• Lack of it caused infertility in soil , fertilizer is used frequently , therefore the
phosphorous cycle is substantially affected
• Phosphorus pollution has contributed to the eutrophication of many water
bodies and may also affect natural food chains

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Nutrients Cycle (Sulphur


cycle)
• Basic constituent of proteins in plants and animals
• Sulphur dioxide (SO2)and hydrogen sulphide (H2S) are important gaseous forms
• Sulphate ion ( SO42-) is the common form found in water and soil
• Sulphate ion is reduced after being absorbed from the soil by plants and bacteria
and utimately incorporated as sulphydryl group (-SH) in proteins. Some sulphates
are reduced under anaerobic conditions directly to sulphides, including H2S or to
elemental sulphur by a class of bacteria known as desulfovibrio found in ocean
bottom
• Thus the hydrogen sulphide (H2S) escapes as a gas into the atmosphere and
replenishes the sulphur lost as precipitaion.
• In the presence of oxygen, H2S is rapidly oxidised to sulphates by bacteria of
genus Thiobacillus
• Even in absence of oxygen several types of bacteria oxidise H2S to elemental
sulphur
• Atmosphere receives sulphur through bacterial emission (H2S), fossil fuel burning
(SO2)sea salts (SO42-)and some volcanic emissions ( H2S, SO2, SO42-)
• The sulphates and acid then precipitates with rain
• Sulphur cycle is overloaded due to burning of fossil fuels at an ever increasing
rates

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Nutrients Cycle (Sulphur


cycle)

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Environmental Pollution Control


ETZC362/PEZC411

Prof. Krishna C. Etika


BITS Pilani Associate Professor
Pilani Campus Department of Chemical Engineering
B.I.T.S-Pilani, Pilani Campus

Lecture-2
06-08-2023
BITS Pilani
Pilani Campus

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Handout
Topics Lecture No
Impact of Man on the Environment: An Overview 1
Air Pollution: Sources and Effects 2
Meteorological Aspects of Air Pollutant Dispersion 3-4
Air Pollution Sampling and Measurement 5
Air Pollution Control Methods & Equipment 6-7
Review 8
Water Pollutants 9
Wastewater Sampling and Analysis 10
Waste Water Treatment 11-13
Hazardous Waste Management 14
Noise Pollution 15
Review 16

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Consequences of Population
Growth
• Factor degrading environment is population growth
• Famine and pestilence kept population under control
• With the advent of chemical compounds to restore and
enhance soil fertility and to help protect domesticated
species man was able to extend food producing capacity
significantly
• Modern medicine have helped reduce human mortality
• Therefore it is important to assess growth population to
understand impact of population on environments
– Reasons for lower death rate (food production, cheap
energy sources, industrial revolution)

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Consequences of Population
Growth

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Exponential Growth
k = population growth rate

Doubling Time (Td) for Exponential Growth: Time taken to double the population, i.e.,

r = percent rate of growth


= (100 x k)
= (b-d+m)
b=percent birth rate
d=percent death rate
m=percent migration rate6
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Problem 1

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Solution

Given,

Po = 1 billions
to = 2000
t= 2020
k = 1.6% = 0.016
P=?

P = 1x exp (0.016 x (2020-2000)


= 1.377 billions

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Solution

Given,

Po = 1.377 billions
to = 2020
t= 2050
k = 1.2% = 0.012
P=?

P = 1.377x exp(0.012 x (2050-2020)


= 1.974 billions

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Population Growth Rate India

If we assume that population growth rate will be


the average of last five years in the future

Then k = 0.86% = 0.0086

Doubling time: 0.693/0.86 = 80 years (Year 2103)


Estimated Population: 2.856 Billion

If k = 1.7% = 0.017

Doubling time: 41 years (Year 2064!)

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World Population & Energy


Consumption

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Effect of Population on Energy


Consumption
“Nature has enough for
satisfying everybody’s Desire for more and
need but not for more comfort
anybody’s greed”.

Nature has created the In the last 300 years we


coal and petroleum in have consumed most of
millions of years and we the coal and almost all
have exhausted them in of the petroleum
hundreds of years. products. Two main reasons for this
growth in energy
consumption

Per capita energy


Exponential growth of
consumption rate which
world’s population
is also exponential

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ENERGY CONSUMTION AND


DEMAND
Previously only marginal utilization of energy was realized.
The present industrial civilization became possible only
when supply of fossil fuels was tapped by mining of coal
about 900 years ago and oil 150 years ago.

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ENERGY CONSUMTION AND


DEMAND
Improvements in technology for discovery and utilization of
fossil fuels.
Two main reasons for this growth in energy consumption
• Exponential growth of world’s population

• Total energy consumption of the world

• Per capita energy consumption rate which is also


exponential

l = per capita energy consumption growth rate = j - k 14


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ENERGY CONSUMTION AND


DEMAND
 NOTE: EVEN IF per capita energy consumption growth
rate = 0, even then,

 World Energy Consumption Growth Rate will rise


exponentially! Why?

 What does that mean? How can per capita energy


consumption growth rate be ZERO??

 Exponential rise in demand for energy will put lot of


extra burden on fossil fuels – More Pollution and
Environmental Impact.
WE MUST CONTROL THE POLLUTION
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Pollution Mitigation

Pollution
Mitigation

Pollution Pollution
Prevention Control

Measures taken after


Avoiding or minimizing
wastes have been
the generation of
produced to limit the
wastes that produce
damage they may
pollutants
cause

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Pollution Prevention

increasing efficiency in energy use

use of environmentally benign fuel sources.

Modifying a production process to produce less


waste

Using non-toxic or less toxic chemicals as cleaners,


degreasers and other maintenance chemicals

Implementing water and energy conservation


practices

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Weather Vs Climate

What is the difference between weather


and climate?

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Weather Vs Climate
o Weather : atmospheric conditions that occur locally
over short periods of time—from minutes to hours
or days. Example: rain, snow, clouds, winds, floods,
or thunderstorms.

o Climate: the long-term (usually at least 30 years)


regional or even global average of temperature,
humidity, and rainfall patterns over seasons, years,
or decades.
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Climate Change

o Climate change is a long-term change in the average


weather patterns that have come to define Earth’s local,
regional and global climates. These changes have a
broad range of observed effects that are synonymous
with the term.

o Is it Real???

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Climate Change

https://climate.nasa.gov/

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Climate Change

o Global temperatures are now at their highest since


records began. In fact, 17 of the 18 warmest years on
record have all taken place since 2001.

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Climate Change: Causes


Human activities are driving the global
warming trend observed since the mid-
20th century.
o The greenhouse effect is essential to life on Earth, but
human-made emissions in the atmosphere are trapping and
slowing heat loss to space.

o Five key greenhouse gases are water vapor, carbon


dioxide (CO2), methane (CH4), nitrous oxide (N2O) and
ozone (O3).

o Is it only the GHGs or the Sun has become


hotter?
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Climate Change: Causes

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Greenhouse Effect

The greenhouse effect: some of the infrared radiation from the Sun passes through the
atmosphere, but most is absorbed and re-emitted in all directions by greenhouse gas
molecules and clouds. The effect of this is to warm the Earth’s surface and the lower
atmosphere.
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Greenhouse Effect

o Do all gas molecules absorb and re-emit infrared


energy?

Molecules that have just two atoms


vibrate by simply moving closer together
and then further apart. The nitrogen (N2)
and oxygen (O2) molecules vibrate in this
simple mode.

 Molecules with more (and more complex!) vibration modes are more likely to interact
with passing waves of electromagnetic radiation.
 This is why carbon dioxide absorbs and emits infrared (IR) radiation, while nitrogen and
oxygen molecules do not.
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Global Warming Potential


(GWP)
o The Global Warming Potential (GWP) was developed to
allow comparisons of the global warming impacts of
different gases.

o It is a measure of how much energy the emissions of 1


ton of a gas will absorb over a given period of time (100
years), relative to the emissions of 1 ton of carbon
dioxide (CO2).

o The larger the GWP, the more that a given gas warms
the Earth compared to CO2 over that time period.

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Global Warming Potential


Methane (CH4) is estimated to have a GWP of 27-30 over
100 years

Nitrous Oxide (N2O) has a GWP 273 times that of CO2 for a
100-year timescale

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Why Not Reduce Water


Vapor?
Because….
o A 100 year GWP for H2O is 10−3 to 5 × 10−4

o It does not regulate earth’s temperature in a way that


other CHGs do

o It is condensable below a certain temperature

o However, the presence of other CHGs are increasing the


water vapor concentration leading to increased warming.

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Ozone Depletion

 Ozone layer in the stratosphere serves as a shield protecting


the earth surface from the sun’s deadly ultraviolet radiation .

 Chlorofluorocarbons (CFC) when used in air conditioner and


refrigeration were valued for their stable and non toxic
properties. However,

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Environmental engineering

• The application of science and engineering principles,


under constraint, to the protection and enhancement of
the quality of the environment and to the enhancement
and protection of public health and welfare

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Major Pollution Issues

Water

Pollution

Solid
Air
Waste
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Air Pollution
What is “Air Pollution”
Any atmospheric condition in which certain substances are present in
such concentrations that they can produce undesirable effects on man
and his environment.
– These substances include
• Gases ( sulphur oxides, nitrogen oxides, carbon monoxide, hydrocarbons etc)
• Particulate matter (smoke, dust, fumes, aerosols)
• Radioactive materials and many others

A particular substance is termed as a pollutant only when its


concentration is relatively high compared with the background
value and causes adverse effects
Example : if SO2 if present in atmosphere greater than the background
value of 2 x 10-4 ppm and causes measurable effects on
humans, animals, plants etc

Pollutants are naturally present in low (background) concentration.


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Background Concentration of
Pollutants

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Air Quality Index

o The AQI will consider eight pollutants (PM10, PM2.5, NO2, SO2,
CO, O3, NH3, and Pb) for which short-term (up to 24-hourly
averaging period) National Ambient Air Quality Standards
are prescribed.

o Based on the measured ambient concentrations,


corresponding standards and likely health impact, a sub-index
is calculated for each of these pollutants.

o The worst sub-index reflects overall AQI.

o Associated likely health impacts for different AQI categories


and pollutants have been also been suggested, with primary
inputs from the medical expert members of the group.
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Air Quality Index


The AQI values and corresponding ambient concentrations (health breakpoints) as well as
associated likely health impacts for the identified eight pollutants are as follows:

* CO in mg/m3 , and other pollutants in µg/m3; 24h-hourly average values for PM10,
PM2.5, NO2, SO2, NH3, and Pb, and 8-hourly values for CO and O3.
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Air Quality Index

Based on the measured ambient concentrations of a pollutant, sub-index is calculated,


which is a linear function of concentration
(e.g. the sub-index for PM2.5 will be 51 at concentration 31 µg/m3, 100 at
concentration 60 µg/m3, and 75 at concentration of 45 µg/m3).

The worst sub-index determines the overall AQI.


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Calculation of AQI

Ip = [IHi – ILo / BPHi – BPLo] (Cp – BPLo) + ILo

Ip = index of pollutant p
Cp = truncated concentration of pollutant p
BPHi = concentration breakpoint i.e. greater than or equal to Cp
BPLo = concentration breakpoint i.e. less than or equal to Cp
IHi = AQI value corresponding to BPHi
ILo = AQI value corresponding to BPLo

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Problem 2
Calculate AQI on the basis of PM2.5 If the current concentration
of PM2.5 is 110 ug/m3

Ip = [IHi – ILo / BPHi – BPLo] (Cp – BPLo) + ILo


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Solution

Ip = ?
Cp = 110 ug/m3
BPHi = 120
BPLo = 91
IHi = 201
ILo = 300

Ip= [(300-201)/ (120-91)] (110-91) + 201 = 265.86

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Scales of Concentration
Concentration of the pollutants in atmosphere can be
expressed as
• Mass concentration
– 𝓶𝒑: mass of the pollutant
– 𝓶𝒂 : mass of the pure air in given air-pollutant mixture

• Volume concentration
– 𝒚𝒑: volume concentration
– 𝒗𝒑 : volume of pollutant
– 𝒗𝒑 : volume of pure air

• Volume concentration in ppm


• Mass-volume concentration

• 𝜌𝒑: Micrograms of pollutants per cubic meters air 𝛍𝒈/𝒎3


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Scales of Concentration
A number of relationship can be developed among these
concentrations

Assuming ideal Gas Law for pollutants we get the following

M𝒑 molecular weight of pollutant , T is temperature in K and 8.314 x


10-2 is universal gas constant expressed as m3-bar/kg-mol-K
T= 25oC, Pressure = 1.0133 bars the equation reduces to

Substituting we get
𝜌𝒑
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Problem 2

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END OF LECTURE

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Solution

Given Data

yppm=35

yp = 35x10-6 m3 of CO/m3 of Air

But we need to determine the mass fraction,

How to determine the mass of 35x10-6 m3 of CO ?

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Solution

Assume CO is an “Ideal Gas” and Use Ideal Gas Law

PV= n RT

PV = (m/M)xRT
M= Molecular Weight of CO
= 28 g/mol
 mCO = (PVM) / RT
P = 1 bar, V= 35 x 10-6 m3, M = 28 g/mol,
R= 8.314 x 10-2m3-bar/kg-mol-K = 0.008312 x 10-2m3-bar/g-mol-K
, T = 298 K

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Solution

Assume Air is an “Ideal Gas” and Use Ideal Gas Law

PV= n RT

PV = (m/M)xRT
M= Molecular Weight of Air
= 29 g/mol
 mair = (PVM) / RT
P = 1 bar, V= 1 m3, M = 29 g/mol,
R= 8.314 x 10-2m3-bar/kg-mol-K = 0.008312 x 10-2m3-bar/g-mol-K
, T = 298 K

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Solution

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Problem 4

Example
CO is present in standard atmospheric air (25 oC , 1 atm)
at a concentration of 50 ppm. Compute 𝒚𝒑, 𝜌𝒑, 𝒑 values
 Solution
Given data:
Concentration of CO = 50 ppm
Volume concentration, yp = yppm x 10-6 = 50 x 10-6 = 5 x
10-5
Mass volume concentration, ρp
M P y ppm (10 3 ) 28(50)10 3
P    57.26  10 3 μg/m 3  57.26  10 6 kg/m 3
24.45 24.45
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Scales of Concentration
Example
The mass concentration wp, can be calculated as follows:
Divide mass concentration to volume concentration equation

wp mp  v a  v p 
  
yp v p  ma  m p 

But the term (ma+mp/va+vp) can be written as


ma  m p ma mp
 (1  y a )  yp
va  vp va vp

Taking the density of air, ρa, as equal to ma/va, and density of pollutant, ρp =
(mP/vP)yp; we get
p 57.26  10 6
wp    0.000048
 a (1  y p )   p 1.185(1  0.00005)  57.26  10 6
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Air pollutant classification


Based on physical state
– Pollutants that are gases or particulates
– Gases, such as sulfur dioxide and nitrogen oxides
– Particulates represent any dispersed matter, solid or liquid, in which the individual
aggregates are larger than single small molecules (about 0.0002 m in diameter) but smaller
than about 500 micrometers
Based on formation
– Primary pollutants
• Emitted directly from the sources
• Include ash, smoke, dust, fumes, mist, spray, etc
• Include inorganic gases such that SO2, H2S, olefinic,
aromatic hydrocarbons, CO,CO2, H2F, etc
– Secondary pollutants
• Formed in the atmosphere by chemical interactions among
primary pollutants and normal atmosphere constituents
• Include SO3, NO2, ozone, aldehydes, ketones, various
sulphates & nitrates salts
Based on source
– Natural & anthropogenic sources
– Natural sources include: wind blown dust, volcanic ash and gases etc…
– Anthropogenic sources include: industry, agriculture etc…

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Properties of air pollutants

Particulate matters
– Refers to all atmospheric substances that are not gases
– Can be suspended particles or solid particles or mixtures of two
– Can be composed of inert of extremely reactive materials (100 µm or 0.1 µm or
less)
– Classification include:
• Dust
• Smoke
• Fumes
• Mist
• Fog
• Aerosols

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Properties of air pollutants

Particulate matters
• Dust: particle size 1-200 𝛍m
• Natural disintegration of rock, grinding, spraying
• Large settling velocity, removed by gravity
• Smoke: fine particles 0.01-1 𝛍m
• Combustion and other chemical processes
• Can be liquid or solid and have different colours
• Fumes: particle size 0.1-1 𝛍m
• Solid particles released from chemical or metallurgical processes
• Mist: smaller than 10 𝛍m
• Liquid droplets formed by condensation in the atmosphere or from industrial processes
• Fog: mist in which liquid is water
• Aerosol: smaller than 1 𝛍m
• All air born suspensions solid or liquid

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Properties of air pollutants

Oxides of sulphur
– Most important emitted oxide is SO2
– Oxidised slowly in clean air to SO3
– Both SO2 & SO3 relatively quickly washed out of the atmosphere by rain
Nitrogen oxides
– Out of six or seven oxides of nitrogen NO2, NO & N2O are found in appreciable
quantities in atmosphere
– All the oxides are major concern as they are pollutants
Carbon monoxides
– Constitutes the single largest pollutant in the urban atmosphere
– Has a B.Pt of -192 0C
– Affinities towards hemoglobin in blood stream & is dangerous asphyxiant
– Main sources of CO in urban air are smoke, exhaust fumes, from devices
burning coal, gas or oil

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Effects of air pollutants

Human effects
• Acute effects
• Short term exposure to air pollutants at high
concentrations
• Chronic effects
• Continuous exposure to air pollutants at low
concentrations
• Effects occur by continuous irritation by pollutants
which interact with environmental or biological
factors

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Effects of air pollutants

Respiratory effects
Pollutants enter the body in number of ways
Cause eye and skin irritation
Certain particulates swallowed as a result of internal
respiratory cleaning action
Particulate matter inhaled may be deposited in
various regions of the respiratory system depending
on particle size

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Effects of air pollutants

Particulate matter
Toxic effect of particles can be grouped into three categories
Interference of inert particles with the cleaning mechanisms
of the respiratory tract
Particles act as carriers of adsorbed toxic because of their
physical or chemical characteristics
Particles may be intrinsically toxic because of their physical
or chemical characteristics

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Effects of air pollutants

Lead
It is neurotoxic whose poisoning results in convulsions, severe
and irreversible brain damage, and death
Inhaled lead is far more serious than ingested lead
Particles emitted by automobile are retained within lungs and
absorbed by body with an efficiency of 40%
Body maintains about 15-25 µg of lead per 100g of whole
blood

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Effects of air pollutants

Cadmium
It is potential health hazard due to its presence in urban
atmosphere and cigarette smoke
Natural Cd levels in air vary from 0.002 µg/m3 to much
higher values of about 0.3 µg/m3 found near zinc smelters
Exposure to fumes or oxides of Cd is known to cause
cardiovascular diseases
Cd can interfere with the proper zinc and copper metabolism
in the body

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Effects of air pollutants

Nickel
Nickel carbonyl is emitted into the atmosphere and it is formed in
tobacco smoke
Within lung, carbonyl complex breaks down and deposits
finely divided nickel which is main cause of cancer in lungs
Nickel carbonyl cause changes in alveoli of lungs resulting in
respiratory damage symptoms

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Effects of air pollutants

Mercury
Present in atmosphere because of its relatively high vapor
pressure
Gaseous mercury is washed from air by rain
Inorganic mercury is converted into its methyl or dimethyl
compounds by the action of bacteria
Mercury poisoning include neurological damage,
chromosomal aberrations and even death

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Effects of air pollutants

Oxides of nitrogen
 Major oxides of nitrogen which affect human health are nitric
oxide (NO) and nitrogen dioxide (NO2)
 NO2 is insoluble and upon inhalation can reach moisture filled
alveoli of lungs
 It is converted to nitrous and nitric acids which are highly
irritating and cause damage to lungs
 Long term exposure to concentrations of order of 1 ppm could
lead to biochemical alterations in blood

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Effects of air pollutants

Sulphur Dioxide
Aggravates existing respiratory diseases
Broncho constriction when exposed for a few minutes to
levels of 1.6 ppm
Formation of H2SO4, sulphate aerosols SO3 etc in the atm.
CO
CO+Hb  COHb
Has 210 times greater affinity to hemoglobin than O2
Tissues are deprived of O2

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Effects of air pollutants

Air pollution effects on vegetation


affects the leaf structure
Caused damage such as necrosis, chlorosis, epinasty
Cement dust affect the vegetation
Chemicals such as arsenic and fluorides when deposited on
leaves poison animals

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Behaviour and Fate of


Pollutants
Natural Pathways of exchange of pollutants from atmosphere to
earth surface (Scavenging Processes).
Particulates :
• Wet removal by precipitation
• Dry removal by sedimentation, impaction and diffusion
Gases:
• Wet removal by precipitation
• Chemical reaction in the atmosphere to produce
aerosols and absorption on aerosols with subsequent
removal
• Absorption or reaction at land and ocean surfaces

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Wet precipitation

Wet precipitation has two distinct mechanisms- “rainout” and


“washout”
Rainout:
 Various processes taking place inside clouds
 Contaminants serve as condensation nuclei on which droplets
condense
 Effective for particle size less than 0.1 m

Washout:
 Removal of pollutants below the cloud level by falling rain
 Effective in removing particles >2 m

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Dry deposition

(Accounts for about 20% of total particulate matter removal from


the atmosphere)
 Sedimentation
 Inertial impaction
 Diffusion
Sedimentation:
Particulate matter smaller than 0.1 m often coagulates through
mutual collisions and forms larger aggregates which are
effectively removed by gravitational settling. The rate of
settling of the particles depends on their settling velocities
according to the stokes’ law: gd 2  
vt 
p
   a 1 
2C 
 d p
18 a
p
 p 

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Dry deposition
vt = terminal settling velocity; dp = particle diameter; p and a = density of
particle and air, respectively; a = viscosity of air; P = air pressure; C =
constant
 Rate of sedimentation is strongly influenced by the particle size
 Particles larger than 10 m have high settling rates and hence have short
residence time in the atmosphere
Inertial impaction
Windborne particles strike on obstacle and are deposited

Diffusion
Small particles migrate to land and ocean surfaces
 Rate of sedimentation is strongly influenced by the particle size
 Particles larger than 10 m have high settling rates and hence have short
residence time in the atmosphere

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Interaction at the Earth’s surface

 Absorption
 Adsorption
 Biological action in Soil

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Interaction at the Earth’s surface


ABSORPTION
At the ocean surface SO2 first diffuses through the gas phase, crosses
the gas-liquid interface, and finally diffuses into the bulk of the
ocean where it is absorbed. NO2 also absorbed by ocean and other
surface waters.
ADSORPTION
SO2 first diffuses to the external surface of the solid, penetrates into the
pores of the solid, and is subsequently adsorbed on the pore site

BIOLOGICAL ACTION IN SOIL


Soil contains certain bacteria which can make use of CO in their
metabolism, producing either CO2 or CH4.
2CO  O2  2CO2
CO  3H 2  CH 4  H 2O
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Chemical Reaction in the


Atmosphere
SO2 is oxidized to SO3 which combines with atmospheric
moisture to form H2SO4 mist(Slow process)
2 SO2  O2  2SO3
H 2O  SO3  H 2 SO4 (Removed by wet precipitation)

Metal salt particles serve as nucleation sites for droplet formation and
react with H2SO4 to produce sulphates, which are also removed by wet
precipitation
2 NaCl  H 2 SO4  Na2 SO4  2 HCl

Direct conversion of NO2 to HNO3 in presence of moisture (slow


process).
3NO2  H 2O  2 HNO3  NO

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Air pollution laws and


standards
The air (prevention and control of pollution) act, 1981
An Act to provide for the prevention, control and abatement of air
pollution, for the establishment, with a view to carrying out the
aforesaid purposes, of Boards, for conferring on and
assigning to such Boards powers and functions relating
thereto and for matters connected therewith.
It extends to the whole of India.
Central Board for the Prevention and Control of Air
Pollution
State Boards for the Prevention and Control of Water
Pollution to be, State Boards for the Prevention and
Control of Air Pollution

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The air act, 1981


Functions of Central Board
• Advise the Central Government on any matter concerning the improvement of
the quality of air and the prevention, control or abatement of air pollution.
• Plan and cause to be executed a nation-wide programme for the prevention,
control or abatement of air pollution
• Co-ordinate the activities of the State and resolve disputes among them
• Provide technical assistance and guidance to the State Boards, carry out and
sponsor investigations and research relating to problems of air pollution and
prevention, control or abatement of air pollution;
• Plan and organize the training of persons engaged or to be engaged in
programs for the prevention, control or abatement of air pollution on such terms
and conditions as the Central Board may specify;
• Organize through mass media a comprehensive program regarding the
prevention, control or abatement of air pollution;
• Collect, compile and publish technical and statistical data relating to air pollution
and the measures devised for its effective prevention, control or abatement and
prepare manuals, codes or guides relating to prevention, control or abatement
of air pollution;
• Lay down standards for the quality of air.
• Collect and disseminate information in respect of matters relating to air pollution

Ref: http://www.envfor.nic.in/legis/air/air1.html
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The air act, 1981


Functions of State Boards
• To plan a comprehensive program for the prevention, control or abatement of air pollution
and to secure the execution thereof.
• To advise the State Government on any matter concerning the prevention, control or
abatement of air pollution
• To collect and disseminate information relating to air pollution.
• To collaborate with the Central Board in organizing the training of persons engaged or to be
engaged in programs relating to prevention, control or abatement of air pollution and to
organize mass-education program relating thereto;
• To inspect, at all reasonable times, any control equipment, industrial plant or manufacturing
process and to give, by order, such directions to such persons as it may consider
necessary to take steps for the prevention, control or abatement of air pollution
• To inspect air pollution control areas at such intervals as it may think necessary, assess the
quality of air therein and take steps for the prevention, control or abatement of air pollution
in such areas
• To lay down, in consultation with the Central Board and having regard to the standards for
the quality of air laid down by the Central Board, standards for emission of air pollutants
into the atmosphere from industrial plants and automobiles or for the discharge of any air
pollutant into the atmosphere from any other source whatsoever not being a ship or an
aircraft
• To advise the State Government with respect to the suitability of any premises or location
for carrying on any industry which is likely to cause air pollution;
• To Perform such other functions as may be prescribed or as may, from time to time, be
entrusted to it by the Central Board or the State Government;
Ref: http://www.envfor.nic.in/legis/air/air1.html
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The air act, 1981

The state PCBs are empowered to


Close, prohibit or regulate any industry, operation or
process
Grant consent within four months after receiving an
application and if the application is rejected, allow the
industry to appeal to the appellate authority for grant of
consent
Bar any legal proceedings or law suits against the
government or the officials of the Board for actions taken
in pursuance of the act

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Standards

• Legal standards for ambient air quality are prescribed by


the govt
• Purpose of these standards is to reduce the pollutants to
a certain level which would avoid undesirable effects
• In India, various areas of a state are classified by the
concerned PCBs into three categoris
• Industrial and mixed use areas
• Residential and rural areas
• Sensitive areas

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National Ambient Air Quality


Standards

Ref: http://www.cpcb.nic.in/National_Ambient_Air_Quality_Standards.php
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National Ambient Air Quality


Standards

Ref: http://www.cpcb.nic.in/National_Ambient_Air_Quality_Standards.php
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Environmental Pollution Control


ETZC362/PEZC411

Prof. Krishna C. Etika


BITS Pilani Associate Professor
Pilani Campus Department of Chemical Engineering
B.I.T.S-Pilani, Pilani Campus

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Re-CAP

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ENERGY CONSUMTION AND


DEMAND
Improvements in technology for discovery and utilization of
fossil fuels.
Two main reasons for this growth in energy consumption
• Exponential growth of world’s population

• Total energy consumption of the world

• Per capita energy consumption rate which is also


exponential

l = per capita energy consumption growth rate = j - k 3


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Weather Vs Climate
o Weather : atmospheric conditions that occur locally
over short periods of time—from minutes to hours
or days. Example: rain, snow, clouds, winds, floods,
or thunderstorms.

o Climate: the long-term (usually at least 30 years)


regional or even global average of temperature,
humidity, and rainfall patterns over seasons, years,
or decades.
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Greenhouse Effect

The greenhouse effect: some of the infrared radiation from the Sun passes through the
atmosphere, but most is absorbed and re-emitted in all directions by greenhouse gas
molecules and clouds. The effect of this is to warm the Earth’s surface and the lower
atmosphere.
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Air Pollution
What is “Air Pollution”
Any atmospheric condition in which certain substances are present in
such concentrations that they can produce undesirable effects on man
and his environment.
– These substances include
• Gases ( sulphur oxides, nitrogen oxides, carbon monoxide, hydrocarbons etc)
• Particulate matter (smoke, dust, fumes, aerosols)
• Radioactive materials and many others

A particular substance is termed as a pollutant only when its


concentration is relatively high compared with the background
value and causes adverse effects
Example : if SO2 if present in atmosphere greater than the background
value of 2 x 10-4 ppm and causes measurable effects on
humans, animals, plants etc

Pollutants are naturally present in low (background) concentration.


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Air Quality Index

o The AQI will consider eight pollutants (PM10, PM2.5, NO2, SO2,
CO, O3, NH3, and Pb) for which short-term (up to 24-hourly
averaging period) National Ambient Air Quality Standards
are prescribed.

o Based on the measured ambient concentrations,


corresponding standards and likely health impact, a sub-index
is calculated for each of these pollutants.

o The worst sub-index reflects overall AQI.

o Associated likely health impacts for different AQI categories


and pollutants have been also been suggested, with primary
inputs from the medical expert members of the group.
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Air Quality Index


The AQI values and corresponding ambient concentrations (health breakpoints) as well as
associated likely health impacts for the identified eight pollutants are as follows:

* CO in mg/m3 , and other pollutants in µg/m3; 24h-hourly average values for PM10,
PM2.5, NO2, SO2, NH3, and Pb, and 8-hourly values for CO and O3.
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Calculation of AQI

Ip = [IHi – ILo / BPHi – BPLo] (Cp – BPLo) + ILo

Ip = index of pollutant p
Cp = truncated concentration of pollutant p
BPHi = concentration breakpoint i.e. greater than or equal to Cp
BPLo = concentration breakpoint i.e. less than or equal to Cp
IHi = AQI value corresponding to BPHi
ILo = AQI value corresponding to BPLo

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Scales of Concentration
Concentration of the pollutants in atmosphere can be
expressed as
• Mass concentration
– 𝓶𝒑: mass of the pollutant
– 𝓶𝒂 : mass of the pure air in given air-pollutant mixture

• Volume concentration
– 𝒚𝒑: volume concentration
– 𝒗𝒑 : volume of pollutant
– 𝒗𝒑 : volume of pure air

• Volume concentration in ppm


• Mass-volume concentration

• 𝜌𝒑: Micrograms of pollutants per cubic meters air 𝛍𝒈/𝒎3


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Scales of Concentration
A number of relationship can be developed among these
concentrations

Assuming ideal Gas Law for pollutants we get the following

M𝒑 molecular weight of pollutant , T is temperature in K and 8.314 x


10-2 is universal gas constant expressed as m3-bar/kg-mol-K
T= 25oC, Pressure = 1.0133 bars the equation reduces to

Substituting we get
𝜌𝒑
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Problem 3

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Solution

Given Data

yppm=35

yp = 35x10-6 m3 of CO/m3 of Air

But we need to determine the mass fraction,

How to determine the mass of 35x10-6 m3 of CO ?

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Solution

Assume CO is an “Ideal Gas” and Use Ideal Gas Law

PV= n RT

PV = (m/M)xRT
M= Molecular Weight of CO
= 28 g/mol
 mCO = (PVM) / RT
P = 1 bar, V= 35 x 10-6 m3, M = 28 g/mol,
R= 8.314 x 10-2m3-bar/kg-mol-K = 0.008312 x 10-2m3-bar/g-mol-K
, T = 298 K

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Solution

Assume Air is an “Ideal Gas” and Use Ideal Gas Law

PV= n RT

PV = (m/M)xRT
M= Molecular Weight of Air
= 29 g/mol
 mair = (PVM) / RT
P = 1 bar, V= 1 m3, M = 29 g/mol,
R= 8.314 x 10-2m3-bar/kg-mol-K = 0.008312 x 10-2m3-bar/g-mol-K
, T = 298 K

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Solution

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Problem 4

Example
CO is present in standard atmospheric air (25 oC , 1 atm) at
a concentration of 50 ppm. Compute 𝒚𝒑, 𝜌𝒑, 𝒑 values
 Solution
Given data:
Concentration of CO = 50 ppm
Volume concentration, yp = yppm x 10-6 = 50 x 10-6 = 5 x
10-5
Mass volume concentration, ρp
M P y ppm (10 3 ) 28(50)10 3
P    57.26  10 3 μg/m 3  57.26  10 6 kg/m 3
24.45 24.45
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Scales of Concentration
Example
The mass concentration wp, can be calculated as follows:
Divide mass concentration to volume concentration equation

wp mp  v a  v p 
  
yp v p  ma  m p 

But the term (ma+mp/va+vp) can be written as


ma  mp ma m
 (1  yp )  p yp
va  vp va vp

Taking the density of air, ρa, as equal to ma/va, and density of pollutant, ρp =
(mP/vP)yp; we get
p 57.26  10 6
wp    0.000048
 a (1  y p )   p 1.185(1  0.00005)  57.26  10 6
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Air pollutant classification


Based on physical state
– Pollutants that are gases or particulates
– Gases, such as sulfur dioxide and nitrogen oxides
– Particulates represent any dispersed matter, solid or liquid, in which
the individual aggregates are larger than single small molecules (about
0.0002 m in diameter) but smaller than about 500 micrometers
Based on formation
– Primary pollutants
• Emitted directly from the sources
• Include ash, smoke, dust, fumes, mist, spray, etc
• Include inorganic gases such that SO2, H2S, olefinic, aromatic
hydrocarbons, CO,CO2, H2F, etc
– Secondary pollutants
• Formed in the atmosphere by chemical interactions among primary
pollutants and normal atmosphere constituents
• Include SO3, NO2, ozone, aldehydes, ketones, various sulphates &
nitrates salts
Based on source
– Natural & anthropogenic sources
– Natural sources include: wind blown dust, volcanic ash and gases etc…
– Anthropogenic sources include: industry, agriculture etc…
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Properties of air pollutants

Particulate matters
– Refers to all atmospheric substances that are not gases
– Can be suspended particles or solid particles or mixtures of two
– Can be composed of inert of extremely reactive materials (100 µm or 0.1 µm or
less)
– Classification include:
• Dust
• Smoke
• Fumes
• Mist
• Fog
• Aerosols

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Properties of air pollutants

Particulate matters
• Dust: particle size 1-200 𝛍m
• Natural disintegration of rock, grinding, spraying
• Large settling velocity, removed by gravity
• Smoke: fine particles 0.01-1 𝛍m
• Combustion and other chemical processes
• Can be liquid or solid and have different colours
• Fumes: particle size 0.1-1 𝛍m
• Solid particles released from chemical or metallurgical processes
• Mist: smaller than 10 𝛍m
• Liquid droplets formed by condensation in the atmosphere or from industrial processes
• Fog: mist in which liquid is water
• Aerosol: smaller than 1 𝛍m
• All air born suspensions solid or liquid

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Properties of air pollutants

Oxides of sulphur
– Most important emitted oxide is SO2
– Oxidised slowly in clean air to SO3
– Both SO2 & SO3 relatively quickly washed out of the atmosphere by rain
Nitrogen oxides
– Out of six or seven oxides of nitrogen NO2, NO & N2O are found in appreciable
quantities in atmosphere
– All the oxides are major concern as they are pollutants
Carbon monoxides
– Constitutes the single largest pollutant in the urban atmosphere
– Has a B.Pt of -192 0C
– Affinities towards hemoglobin in blood stream & is dangerous asphyxiant
– Main sources of CO in urban air are smoke, exhaust fumes, from devices
burning coal, gas or oil

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Air Pollutants
Classification
• Particulate matter (All atmospheric substances which are
not gaseous)
• Dust – 1-200 m, solid Ca, Al, Si compounds,
• Smoke – 0.01-1 m, liquid or solid Organic compounds
• Fumes – 0.1-1 m, solid Cd, Pb, Hg, Ni
• Mist/Fog - <10 m, liquids

• Gaseous pollutants
• SOx (SO2, SO3)
• NOx (N2O, NO, NO2)
• CO
• Hydrocarbon

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Particulate Matter (PM)

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Effects of air pollutants

Human effects
• Acute effects
• Short term exposure to air pollutants at high
concentrations
• Chronic effects
• Continuous exposure to air pollutants at low
concentrations
• Effects occur by continuous irritation by pollutants
which interact with environmental or biological
factors

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Effects of air pollutants

 Respiratory effects
 Pollutants enter the body in number of ways
 Cause eye and skin irritation
 Certain particulates swallowed as a result of internal
respiratory cleaning action
 Particulate matter inhaled may be deposited in various
regions of the respiratory system depending on particle
size

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Effects of air pollutants

Oxides of nitrogen
 Major oxides of nitrogen which affect human health are
nitric oxide (NO) and nitrogen dioxide (NO2)
 NO2 is insoluble and upon inhalation can reach moisture
filled alveoli of lungs
 It is converted to nitrous and nitric acids which are highly
irritating and cause damage to lungs
 Long term exposure to concentrations of order of 1 ppm
could lead to biochemical alterations in blood

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Effects of air pollutants

Sulphur Dioxide
 Aggravates existing respiratory diseases
 Broncho constriction when exposed for a few minutes to
levels of 1.6 ppm
 Formation of H2SO4, sulphate aerosols SO3 etc in the
atm.
CO
CO+Hb  COHb
Has 210 times greater affinity to hemoglobin than O2
Tissues are deprived of O2

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Effects of air pollutants

Particulate matter
Toxic effect of particles can be grouped into three
categories
Interference of inert particles with the cleaning
mechanisms of the respiratory tract
Particles act as carriers of adsorbed toxic because of
their physical or chemical characteristics
Particles may be intrinsically toxic because of their
physical or chemical characteristics

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Effects of air pollutants

Lead
 It is a neurotoxic whose poisoning results in
convulsions, severe and irreversible brain damage, and
death
 Inhaled lead is far more serious than ingested lead
 Particles emitted by automobile are retained within
lungs and absorbed by body with an efficiency of 40%
 Body maintains about 15-25 µg of lead per 100g of
whole blood

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Effects of air pollutants

Cadmium
 It is potential health hazard due to its presence in urban
atmosphere and cigarette smoke
 Natural Cd levels in air vary from 0.002 µg/m3 to much
higher values of about 0.3 µg/m3 found near zinc
smelters
 Exposure to fumes or oxides of Cd is known to cause
cardiovascular diseases
 Cd can interfere with the proper zinc and copper
metabolism in the body

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Effects of air pollutants


Nickel
 Nickel carbonyl is emitted into the atmosphere and it is
formed in tobacco smoke
 Within lung, carbonyl complex breaks down and deposits
finely divided nickel which is main cause of cancer in lungs
 Nickel carbonyl cause changes in alveoli of lungs resulting
in respiratory damage symptoms

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Effects of air pollutants


Mercury
 Present in atmosphere because of its relatively high
vapor pressure
 Gaseous mercury is washed from air by rain
 Inorganic mercury is converted into its methyl or
dimethyl compounds by the action of bacteria
 Mercury poisoning include neurological damage,
chromosomal aberrations and even death

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Effects of air pollutants


Air pollution effects on vegetation
 Affects the leaf structure
 Causes damage such as necrosis, chlorosis, epinasty
 Chemicals such as arsenic and fluorides when deposited
on leaves poison animals

Peroxyacyl nitrates or PANs, which are also referred to as acyl peroxy nitrates or APN, are
a component of photochemical smog, produced in the atmosphere when oxidized volatile
organic compounds combine with nitrogen dioxide
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Behaviour and Fate of Pollutants


Natural Pathways of exchange of pollutants from atmosphere
to earth surface (Scavenging Processes).
Particulates :
• Wet removal by precipitation
• Dry removal by sedimentation, impaction and diffusion
Gases:
• Wet removal by precipitation
• Chemical reaction in the atmosphere to produce aerosols
and absorption on aerosols with subsequent removal
• Absorption or reaction at land and ocean surfaces

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Wet precipitation

Wet precipitation has two distinct mechanisms- “rainout” and


“washout”
Rainout:
 Various processes taking place inside clouds
 Contaminants serve as condensation nuclei on which
droplets condense
 Effective for particle size less than 0.1 m

Washout:
 Removal of pollutants below the cloud level by falling rain
 Effective in removing particles >2 m

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Dry deposition
(Accounts for about 20% of total particulate matter removal from the
atmosphere)
 Sedimentation
 Inertial impaction
 Diffusion
Sedimentation:
Particulate matter smaller than 0.1 m often coagulates through mutual
collisions and forms larger aggregates which are effectively removed by
gravitational settling. The rate of settling of the particles depends on their
settling velocities according to the stokes’ law:

gd p2 2C 
vt    a 1  
 d p
18 a
p
 p 
vt = terminal settling velocity; dp = particle diameter; p and a = density of particle and
air, respectively; a = viscosity of air; P = air pressure; C = constant
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Dry deposition

 Rate of sedimentation is strongly influenced by the particle size


 Particles larger than 10 m have high settling rates and hence have
short residence time in the atmosphere
Inertial impaction
Windborne particles strike on obstacle and are deposited

Diffusion
Small particles migrate to land and ocean surfaces
 Rate of sedimentation is strongly influenced by the particle size
 Particles larger than 10 m have high settling rates and hence have
short residence time in the atmosphere

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Interaction at the Earth’s surface

 Absorption
 Adsorption
 Biological action in Soil

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Interaction at the Earth’s surface


ABSORPTION
At the ocean surface SO2 first diffuses through the gas phase, crosses
the gas-liquid interface, and finally diffuses into the bulk of the
ocean where it is absorbed. NO2 also absorbed by ocean and other
surface waters.
ADSORPTION
SO2 first diffuses to the external surface of the solid, penetrates into the
pores of the solid, and is subsequently adsorbed on the pore site

BIOLOGICAL ACTION IN SOIL


Soil contains certain bacteria which can make use of CO in their
metabolism, producing either CO2 or CH4.
2CO  O2  2CO2
CO  3H 2  CH 4  H 2O
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Chemical Reaction in the


Atmosphere
SO2 is oxidized to SO3 which combines with atmospheric
moisture to form H2SO4 mist(Slow process)
2 SO2  O2  2SO3
H 2O  SO3  H 2 SO4 (Removed by wet precipitation)

Metal salt particles serve as nucleation sites for droplet formation and
react with H2SO4 to produce sulphates, which are also removed by wet
precipitation
2 NaCl  H 2 SO4  Na2 SO4  2 HCl

Direct conversion of NO2 to HNO3 in presence of moisture (slow


process).
3NO2  H 2O  2 HNO3  NO

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Air pollution laws and


standards
The air (prevention and control of pollution) act, 1981
• An Act to provide for the prevention, control and abatement of
air pollution, for the establishment, with a view to carrying out
the aforesaid purposes, of Boards, for conferring on and
assigning to such Boards powers and functions relating
thereto and for matters connected therewith.
• It extends to the whole of India.
• Central Board for the Prevention and Control of Air
Pollution
• State Boards for the Prevention and Control of Water
Pollution to be, State Boards for the Prevention and
Control of Air Pollution

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The air act, 1981


Functions of Central Board
• Advise the Central Government on any matter concerning the improvement of
the quality of air and the prevention, control or abatement of air pollution.
• Plan and cause to be executed a nation-wide programme for the prevention,
control or abatement of air pollution
• Co-ordinate the activities of the State and resolve disputes among them
• Provide technical assistance and guidance to the State Boards, carry out and
sponsor investigations and research relating to problems of air pollution and
prevention, control or abatement of air pollution;
• Plan and organize the training of persons engaged or to be engaged in
programs for the prevention, control or abatement of air pollution on such terms
and conditions as the Central Board may specify;
• Organize through mass media a comprehensive program regarding the
prevention, control or abatement of air pollution;
• Collect, compile and publish technical and statistical data relating to air pollution
and the measures devised for its effective prevention, control or abatement and
prepare manuals, codes or guides relating to prevention, control or abatement
of air pollution;
• Lay down standards for the quality of air.
• Collect and disseminate information in respect of matters relating to air pollution

Ref: http://www.envfor.nic.in/legis/air/air1.html
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The air act, 1981


Functions of State Boards
• To plan a comprehensive program for the prevention, control or abatement of air pollution
and to secure the execution thereof.
• To advise the State Government on any matter concerning the prevention, control or
abatement of air pollution
• To collect and disseminate information relating to air pollution.
• To collaborate with the Central Board in organizing the training of persons engaged or to be
engaged in programs relating to prevention, control or abatement of air pollution and to
organize mass-education program relating thereto;
• To inspect, at all reasonable times, any control equipment, industrial plant or manufacturing
process and to give, by order, such directions to such persons as it may consider
necessary to take steps for the prevention, control or abatement of air pollution
• To inspect air pollution control areas at such intervals as it may think necessary, assess the
quality of air therein and take steps for the prevention, control or abatement of air pollution
in such areas
• To lay down, in consultation with the Central Board and having regard to the standards for
the quality of air laid down by the Central Board, standards for emission of air pollutants
into the atmosphere from industrial plants and automobiles or for the discharge of any air
pollutant into the atmosphere from any other source whatsoever not being a ship or an
aircraft
• To advise the State Government with respect to the suitability of any premises or location
for carrying on any industry which is likely to cause air pollution;
• To Perform such other functions as may be prescribed or as may, from time to time, be
entrusted to it by the Central Board or the State Government;
Ref: http://www.envfor.nic.in/legis/air/air1.html
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The air act, 1981

The state PCBs are empowered to


Close, prohibit or regulate any industry, operation or
process
Grant consent within four months after receiving an
application and if the application is rejected, allow the
industry to appeal to the appellate authority for grant of
consent
Bar any legal proceedings or law suits against the
government or the officials of the Board for actions taken
in pursuance of the act

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Standards

• Legal standards for ambient air quality are prescribed by


the govt
• Purpose of these standards is to reduce the pollutants to
a certain level which would avoid undesirable effects
• In India, various areas of a state are classified by the
concerned PCBs into three categoris
• Industrial and mixed use areas
• Residential and rural areas
• Sensitive areas

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National Ambient Air Quality


Standards

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National Ambient Air Quality


Standards

Ref: http://www.cpcb.nic.in/National_Ambient_Air_Quality_Standards.php
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NAAQS by USEPA 2006


Pollutant Primary Stds. Averaging Times Secondary Stds.

Carbon Monoxide 9 ppm (10 mg/m3) 8-hour None

35 ppm (40 mg/m3) 1-hour None

Lead 1.5 µg/m3 Quarterly Average Same as Primary


Nitrogen Dioxide 0.053 ppm (100 µg/m3) Annual (Arithmetic Mean) Same as Primary
Particulate Matter (PM10) Revoked Annual (Arith. Mean)
150 µg/m3 24-hour
Particulate Matter (PM2.5) 15.0 µg/m3 Annual (Arith. Mean) Same as Primary
35 µg/m3 24-hour
Ozone 0.08 ppm 8-hour Same as Primary
0.12 ppm 1-hour(Applies only in limited areas) Same as Primary
Sulfur Oxides 0.03 ppm Annual (Arith. Mean) -------
0.14 ppm 24-hour -------
------- 3-hour 0.5 ppm (1300 µg/m3)

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WHO Air Quality Guidelines


Value
Pollutant Averaging time AQG value
Particulate matter
PM2.5 1 year 10 µg/m3
24 hour(99th percentile) 25 µg/m3

PM10 1 year 20 µg/m3


24 hour(99th percentile) 50 µg/m3

Ozone, O3 Ozone, O3 100 μg/m3


8 hour, daily maximum
Nitrogen dioxide, NO2
1 year 40 μg/m3
1 hour 200 μg/m3

Sulfur dioxide, SO2 24 hour 20 μg/m3


10 minute 500 μg/m3

Source: WHO, 2005. WHO air quality guidelines global update 2005, WHOLIS number E87950
http://www.euro.who.int/__data/assets/pdf_file/0008/147851/E87950.pdf

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ETZC362/PEZC411

Prof. Krishna C. Etika


BITS Pilani Associate Professor
Pilani Campus Department of Chemical Engineering
B.I.T.S-Pilani, Pilani Campus

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Re-CAP

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Scales of Concentration
Concentration of the pollutants in atmosphere can be
expressed as
• Mass concentration
– 𝓶𝒑: mass of the pollutant
– 𝓶𝒂 : mass of the pure air in given air-pollutant mixture

• Volume concentration
– 𝒚𝒑: volume concentration
– 𝒗𝒑 : volume of pollutant
– 𝒗𝒑 : volume of pure air

• Volume concentration in ppm


• Mass-volume concentration

• 𝜌𝒑: Micrograms of pollutants per cubic meters air 𝛍𝒈/𝒎3


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Scales of Concentration
A number of relationship can be developed among these
concentrations

Assuming ideal Gas Law for pollutants we get the following

M𝒑 molecular weight of pollutant , T is temperature in K and 8.314 x


10-2 is universal gas constant expressed as L-bar/mol-K
T= 25oC, Pressure = 1.0133 bars the equation reduces to

Substituting we get
𝜌𝒑
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Air Pollution Sampling


• Most frequently occurring pollutants in an urban environment:
particulate matters (suspended particulate matter i.e. SPM and
respirable suspended particulate matter i.e. RSPM), carbon monoxide
(CO), hydrocarbons (HC), sulfur dioxide (SO2), nitrogen dioxide (NO2)
and photochemical oxidants (O3, PAN, H2O2).

• Sampling and measurement of air pollutants, generally known as air


quality monitoring.

• There are two quite different situations in which the air quality
measurement is undertaken.
1. The ambient air quality measurement where the pollutant levels in the
ambient atmosphere are measured.
2. The measurement of the pollutants emitted from a source such as
smoke stack and is known as stack sampling.
o Stack sampling provides information on the nature and quantities
of various pollutants that are emitted into the atmosphere.
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Air pollution sampling

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Air quality
Monitoring

Measurements of Ambient Air Quality


Emissions - Measures the
quality of all the air
(Stack Sampling) in a particular place.

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Air quality Monitoring


 Most air pollution monitoring equipment performs the act of
sampling and analysis in one action = real time
measurement

 Older equipment = intermittent sampling (time lag between


when the sample was obtained and when data was
available)

 Almost all gaseous pollutants are monitored by real time


analysis - Particulate pollutants are still mostly monitored
by intermittent sampling, even though real time methods
are available

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Ambient Air Sampling

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Ambient Air Sampling


Basic considerations for sampling
• Sample must be representative in terms of time, location, and
conditions to be studied.
• Sample must be large enough for accurate analysis. Most
pollutants = very low levels and require a large volume of gas
for accurate measurement
• The sampling rate must be such as to provide maximum efficiency
of collection.
• Duration of sampling must accurately reflect the fluctuations in
pollution levels i.e. whether 1-hourly, 4-hourly, 6-hourly, 8-hourly,
24-hourly sampling.
• Continuous sampling is preferred.
• Pollutants must not be altered or modified during collection.
pollutants in very small quantities are easy to contaminate. Purge
sampling containers if grab samples are used
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Ambient Air Sampling


• Collection of Gaseous Air Pollutants
• Grab Sampling
• Absorption in Liquids
• Adsorption on Solids
• Freeze-out Sampling
• Collection of Particulate Pollutants
• Sedimentation (Dust fall Jar)
• High-volume Filtration (The Hi-vol. Sampler)
• Tape Sampler
• Impingement
• Electrostatic Precipitation
• Thermal Precipitation

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Ambient Air Sampling

Collection of Gaseous Air Pollutants


Grab Sampling
 Sample is collected by filling an evacuated flask or
inflatable bag.
 Plastic bags are widely used for grab sampling.
 Bag sampling is subject to losses caused by moisture
condensation or diffusion through walls of the bag
 Losses can be minimized by performing analysis
immediately following collection

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Grab Sampling

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Ambient Air Sampling

Collection of Gaseous Air Pollutants


Absorption in liquids
 Absorption separates desired pollutants from air either
through direct solubility in absorbing medium or by
chemical reaction
 Different devices are used which provide a high degree
gas liquid contact
 Most commonly used collector is impinger.
 In impinge, the gas stream is impinged at high velocity
onto a flat surface thus providing good contact between
the gas and liquid.

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Ambient Air Sampling

Collection of Gaseous Air Pollutants


Adsorption in solids
 Based on principle that gases can be adsorbed on
surface of solid materials
 After adsorption, sample gases are desorbed for
analysis. This may be accomplished by heating.
 Most organic vapors are analyzed by gas
chromatograph (GC) techniques

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Ambient Air Sampling

Collection of Gaseous Air Pollutants


Freeze-out sampling
 A series of cold traps, which are maintained at
progressively lower temperature, are used to draw the
air sample where by the pollutants are condensed.
 The samples are brought to the laboratory and are
analysed with gas chromatograph etc.

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Ambient Air Sampling

Collection of particulate pollutants


• Particulate pollutants in atmosphere are grouped into
two categories
• Settle out due to force of gravity
• That remain suspended as aerosols

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Ambient Air Sampling

Collection of particulate pollutants


Sedimentation (Dust fall jar)
 It is effective for collective larger than 10 micron
 Collector consist of plastic jar of about 20 to 35
cm height and 10 – 15 cm diameter at the
base.
 Sample is deposited over a period of one
month and material is dried and weighed
 Dust particles larger then 10 micron seldom
travel more than 1 km. So, dust fall jars must
be spaced near to the emission source.

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Ambient Air Sampling


Collection of particulate pollutants
High-Volume filtration
 Most commonly used particle sampling method
 It is for the particles of size less then 10 micron.
 In this method a known volume of air sampled through a filter
medium and increase in the weight due to trapped particles is
measured (Gravimetric analysis).
 Air-flow is measured by a small flow meter (calibrated in m3
air/minute)
 A glass filter has a collection efficiency of even 99 percent.
 particulate concentration measured is referred to as the
Total Suspended Particles (TSP), = combination of settleable
particles and suspended particles.
expressed as g/m3 for a 24-hour period – normally as part of 6
day cycle
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High Volumer Sampler

https://www.qld.gov.au/environment/management/monitoring/air/air-
monitoring/measuring/samplers
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Ambient Air Sampling


Collection of particulate pollutants
Paper Tape Sampler
 Draw ambient air through a cellulose tape filter
 Sampling time 10 min to 2 hr
 Air is passed through a nozzle and particulates are collected
on the paper tape forming a spot
 Spots are evaluated by analyzing the light that can be
transmitted through the spot.

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COH Degree of Pollution


0-0.9 Light
1-1.9 Medium
2-2.9 Heavy
3-3.9 Very heavy
4-4.9 Extremely heavy

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Ambient Air Sampling

Collection of particulate pollutants


Impingment
 Here the separation of the dust
particles takes place with the
collision against the flat surface.
 Wet impingement is used to
collect particulate in liquid phase.
 These devices have an
advantage of collecting the
sample directly without the need
of filtration.
Andersen cascade impactor

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Stack Sampling

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Stack Sampling
• The major problem in stack sampling: obtaining a
representative sample.
• If a representative sample is not obtained then the
concentration and composition of the actual gas
stream will be different, and serious errors would
result in the analysis.

• The important factors in obtaining a representative


sample: a) selection of the sampling site and b) number
of sampling points required.

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Stack Sampling

• The gas stream in a stack is normally


under turbulent flow conditions and
any flow disturbance would cause
non-uniform and unstable gas flow
profiles and non-uniform particle
concentration patterns.

• The sampling site should be located


at least eight stack or duct
diameters downstream and two
diameters upstream from any
source of flow disturbance such
as, bends, fittings, or constrictions.

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Stack Sampling

• In some stacks, it is not always possible to ensure uniform


flow, so concentration patterns and, hence, multiple
samples are required to obtain a representative sample
• The actual sampling must be performed at a number of
traverse points in the stack
• Other problems associated with stack sampling are the
high temperatures and high velocities of the gases
encountered inside the stack
• High temperature - difficulties in collecting the sample -
require a number of additional measurements: moisture
content, pressure, temperature, the flow rate of the gases
and their compositions.

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Stack Sampling
Sampling System
• Stack sampling is carried out by diverting a part of the gas stream
through a sampling “train” of which a general arrangement is
shown below.
General arrangement of sampling train

6
1 2
3 4 7
5
1. Nozzle
2. Sampling Probe
3. Particulate collector
4. Cooling and/or gas collector
5. Gas flow meter
6. Flow control valve
7. To vacuum pump
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Stack Sampling

Traverse Points
For the sample to become representative, it should be
collected at various points across the stack.
The number of traverse points may be selected as given
below:

https://cpcb.nic.in/openpdffile.php?id=UmVwb3J0RmlsZXMvTmV3SXRlbV8xMTBfaHppbmNpbmVyYXRvci5wZGY=
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Stack Sampling

The sampling site should be


located: at least 8 stack/duct
diameters downstream and 2
diameters upstream from any
source of disturbance.

If not possible then

For rectangular C/S, larger


dimension is the duct diameter.

https://cpcb.nic.in/openpdffile.php?id=UmVwb3J0RmlsZXMvTmV3SXRlbV8xMTBfaHppbmNpbmVyYXRvci5wZGY=
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Stack Sampling
• In circular stacks, traverse points are located at the center of equal
annular areas across two perpendicular diameters

• In case of rectangular stacks, the area may be divided in to 12 to 25


equal areas and the centers for each area are fixed

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Stack Sampling

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Stack Sampling
Particulate Sampling
• The common technique employed for sampling particulate-laden
gas streams is the so called “isokinetic technique”.
• Under isokinetic conditions, the static pressure at the tip of the
probe must be equal to the static pressure in the free stream at
the same cross-section.
• This implies that when two pressures are equalized then the
corresponding velocities must be equal

Isokinetic
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Stack Sampling
Particulate Sampling
• When a sharp-edged probe is introduced into a single-phase fluid stream, the
flow pattern = simple pitot tube.
• The velocity inside the probe is zero and the pressure at the tip of the probe
becomes equal to the stagnation pressure.
• If the gas velocity (up) < free stream velocity (u), is maintained inside the probe,
then the gas flow pattern at the tip of the probe may be represented by given
figure.
• In this case the static pressure at the tip of the probe is greater than the free
stream static pressure at the same cross section

Sub-isokinetic
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Stack Sampling
Particulate Sampling
 If the gas velocity (up), > free stream velocity (u), is maintained inside
the probe, then the gas flow pattern at the tip of the probe may be
represented by given figure.
 In this case the static pressure at the tip of the probe is less than the
free stream static pressure, and too much gas will be sampled in
proportion to the probe area.

Super-Isokinetic
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Stack Sampling

 If sampling velocity > isokinetic rate, the sampling will have a lower mass
concentration of particulate material than the main stream because of greater
percentage of fine particles.

 If the sampling velocity < isokinetic rate, the particulate sample has a higher mass
concentration than actually present, with lower concentration of fine particles.
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Stack Sampling
Particulate Sampling
Isokinetic sampling can be achieved by two ways:
 By computing the point velocity of the free stream
with a pitot tube located as near to the sampling
probe as much as possible without interfering with
the free stream, and then adjusting the sampling
velocity
 By using a null-type sampling probe

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Stack Sampling
• Null type sampling probe: the static pressures measured
between the inner and outer probe walls is balanced
• This (assumes) that the velocity within the probe is equal to
the free stream velocity
• In practice numerous problems are encountered while
trying to maintain true isokinetic conditions because a null
pressure balance does not necessarily indicate a
matched velocity conditions
• The difference in turbulence for duct and probe flow, the
nozzle shape, its surface nonuniformities, possible plugging
of the inner static tap by fine particles, and the location of
the static holes- all these may contribute to nonisokinetic
conditions
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Stack Sampling
Gaseous Sampling
• The basic routine for obtaining a gas sample from stack emission
is similar to that employed in sampling of particulate matter
• The sampling is much easier because it is not necessary to
sample at isokinetic conditions
• The sample can be withdrawn from the stack at a constant rate
independent of the flow rate in the stack
Precautions for obtaining a representative sample
• Particulate matter must be filtered upstream of the collection
system to prevent downstream line plugging as well as to
minimize losses of gaseous pollutants due to reaction with
particulates on cooling
• If moisture is present in stack gases it could get condensed in the
sampling line and dissolve the gaseous constituents of interest
• Suction through the nozzle draws a known volume of the gas
from the stack into a collection device which removes the
constituent gas of interest and the remaining gas is measured
with a flow meter located downstream of the collection device 41
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Analysis of Air Pollutants

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SO2 Measurement

– UV fluorescence analyser
– flame photometric detector (with or without gas
chromatograph)
– electrochemical (coulimetric detector)

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SO2 Measurement
• The measurement of ambient SO2 levels by the UV fluorescence
SO2 analyzer
• Principle: SO2 molecules absorb UV light at the wavelength of 214
nm.
• The absorbed UV energy excites the outer electrons to the next
state.
• The excited electrons then return to the original state and emit
photons at the wavelength of 390 nm.
• The intensity of fluorescence is proportional to the SO2
concentration
• Fluorescence SO2 analyzer consists of a hydrocarbon “kicker”,
fluorescence chamber, light source, photoelectric detector,
electronics, etc
SO2 + hν (UV) SO2*
SO2* SO2 + light
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SO2 Measurement

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NOx Measurement
• Atmospheric nitrogen and any nitrogen in fuel is converted into its oxides,
mainly nitric oxide (NO) and nitrogen dioxide (NO2) during combustion. The
NO oxidizes in presence of O3 (ozone) to form NO2 in the atmosphere.
– NO is an odorless and colourless gas.
– NO2 is a reddish, brown, pungent, acidic gas.
• NO2 is 4 times more dangerous than NO.
– NO2 can irritate the lungs, increase susceptibility and severity of asthma
and lowers resistance to infections such as the flu. Children exposed to
NO2 are at increased risk of respiratory infection.
• The nitrogen oxides are responsible for acid rains that affect the terrestrial
and aquatic life.
• Nitrogen oxides are critical components of photochemical smog - it is
nitrogen dioxide that produces the yellowish brown colour of the smog and
significantly affects visibility.

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NOx Measurement

• Determined using chemiluminescence


• Specific for NO, but total oxides of nitrogen determined
by passing sample over a catalyst to convert NO2 → NO
• Suitable for ambient air containing NOx (NO and NO2) at
levels less than 1 mL/m3
• Reaction of NO with ozone in a dark enclosed chamber
to produce light - detected by a pmt
• Provided the ozone is present in excess the light output
is directly proportional to the concentration of NO
NO + O3 NO2* + O2
NO2* NO2 + h (light)

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NOx Measurement

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CO Measurement

• non-dispersive infra red (NDIR) devices, suitable for


detection from 0-500ppm by volume
• sample through a flow cell in the instrument where it is
irradiated with infrared radiation
• essentially just a modified dual beam infrared
spectrophotometer

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CO Measurement

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Measurement of Volatile
Organic Compounds (VOC)
• Volatile Organic Compounds or VOCs are organic chemicals that
easily vaporize at room temperature. They are called organic because
they contain the element carbon in their molecular structures. VOCs
have no colour, smell, or taste. VOCs include a very wide range of
individual substances, such as hydrocarbons (for example benzene
and toluene), halocarbons and oxygenates.

• Some VOCs are quite harmful, including benzene, polycyclic aromatic


hydrocarbons (PAHs) and 1,3 butadiene.

• Benzene may increase susceptibility to leukaemia, if exposure


is maintained over a period of time.

• PAHs can cause cancer.

• An apparent correlation between butadiene exposure and a


higher risk of cancer.
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Measurement of Volatile
Organic Compounds (VOC)
 A Photo-Ionization Detector measures VOCs and other toxic gases in
low concentrations from ppb (parts per billion) up to 10,000 ppm.
 A Photo Ionization Detector (PID) uses an Ultraviolet (UV) light source
(Photo= light) to break down chemicals to positive and negative ions
(Ionization) that can easily be counted with a Detector.

 Ionization occurs when a molecule absorbs the high energy UV light,


which excites the molecule and results in the temporary loss of a
negatively charged electron and the formation of positively charged ion.
The gas becomes electrically charged. In the Detector these charged
particles produce a current that is then amplified and displayed on the
meter.
 The ions quickly recombine after the electrodes in the detector to
“reform” their original molecule. PIDs are non-destructive; they do not
“burn” or permanently alter the sample gas, which allows them to be
used for sample gathering.
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Measurement of Volatile
Organic Compounds (VOC)
Photo-Ionization Detector (PID)

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Environmental Pollution Control


ETZC362/PEZC411
Prof. Krishna C. Etika
Associate Professor
BITS Pilani Department of Chemical Engineering
Pilani Campus B.I.T.S-Pilani, Pilani Campus

ETZC362/PEZC411 Environmental Pollution Control

Meteorological Aspects of Air


Pollutant Dispersion

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Some Examples

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Inversion at Four Corners power plant

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Inversion in Los Angeles, CA

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The Great Smog of 1952


A severe air-pollution event that affected London
during December 1952.
A period of cold weather, combined with an
anticyclone and windless conditions, collected
airborne pollutants—mostly arising from the use
of coal—to form a thick layer of smog over the
city.
It lasted from Friday 5 December to Tuesday 9
December 1952, and then dispersed quickly
when the weather changed.

This smog killed approximately 12,000 people


and shocked the world into starting the
environmental movement.
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Introduction to Dispersion

 Air pollutants emitted from anthropogenic sources are


transported and diluted in the atmosphere
 Otherwise pollutant concentration reach dangerous
levels near the source of emission
 Effective dispersion of pollutants depend on
Degree of stability
Turbulence

Degree of stability depend on environmental lapse rate

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Temperature Lapse Rates


Lapse Rate (Γ) : rate at which temperature changes with
height in the atmosphere.
Environmental Lapse Rate: The environmental lapse rate
is the cooling or warming as measured by a weather
balloon.
The relationship between the temperature and the altitude can
be obtained by considering air to be an ideal gas.
The change of pressure in the vertical direction may be
represented by the relation:

Where, P = atmospheric pressure, H = altitude, ρ = atmospheric


density
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Temperature Lapse Rates


Also, the ideal gas relation

Where, R = gas constant, T = absolute temperature

General expression for the variation of pressure with altitude

By assuming isothermal atmosphere and integrating the above Eqn.

Where, Po is the pressure at ground level (1.013 bars)


The above equation gives an exponentially decreasing pressure with altitude which is a
typical characteristic of compressible fluids such as air. 9
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Temperature Lapse Rates


Dry Adiabatic Lapse Rate (DALR): rate of change of temperature
with height as a parcel of dry air rises or sinks without exchange of heat with
the surroundings (adiabatic heat exchange).
• As the air parcel rises in the atmosphere, it goes through a region of
decreasing pressure and expands. As it expands, it does work on the
surroundings. Since the process is usually rapid, there is no heat transfer
between the air parcel and the surrounding air.
For the case of an adiabatic process the first law of thermodynamics yields,

 dW  dU
• Since work done by the parcel of dry air, energy is lost to the surroundings
 Internal energy of the air parcel decrease Temperature of the air parcel
decrease.
• The decrease in temperature of a rising, expanding air parcel is an important
feature of vertical air motion.
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Temperature Lapse Rates


The work done on the surroundings is equal to pdV and change in internal energy
becomes equal to CvdT, where Cv is the specific heat at constant volume. By substituting
these terms pdV  C dT  0 V
per unit mass of the air parcel

pdv  cv dT  0
Where v is the specific volume and Cv is the specific heat per unit mass

For a ideal gas, we can write:


R
(Cv  )dT  vdp How??
After rearranging equation, we obtain
MW
dT v  MW

dp MW  Cv  R
The variation of temperature with altitude can be written as a product of two terms:
dT dT dp
 .
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Temperature Lapse Rates

dT MW  g

dh MW  Cv  R

The above expression gives the temperature lapse rate for dry parcel of air moving
upwards adiabatically and is known as dry adiabatic lapse rate.

Now Calculate the DALR

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DALR Calculation
Specific heat capacity: the amount of heat necessary to raise the
temperature of a unit of mass by one Kelvin.

Molar specific heat capacity: amount of heat required to raise the temperature of
1 mol of the gas by 1 ◦C at the constant volume.

Molar Specific Heat Capacity for monatomic ideal gas is 3R/2 and the value for diatomic
ideal gas is 5R/2

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Temperature Lapse Rate

 dT  9.86 o C
  
 dh  adia 1000 meters

Thus, the dry adiabatic lapse rate, Γ is given by

 dT  10 o C
    
 dh  adia 1 km

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Temperature Lapse Rates


In the presence of moisture in the atmosphere, a rising parcel of air may cool until the
partial pressure of water vapor equals the saturation vapor pressure of water. In such
circumstances, some of the water vapor will condense if sufficient nucleation sites are
present and release the latent heat. If λ is the latent heat per gram of water, then the
release of this heat is given by,

dQ    mdw
Where m is the mass of dry air in the parcel and dw is the ratio of the amount of water vapor
which is condensing to the mass of dry air. Adding this term to the right hand side of equation
(8) and proceeding further we get the lapse rate in a saturated condition:

dT g  dw
 
dz C p C p dz
Above equation is referred to as the wet adiabatic lapse rate equation although the process
is not strictly adiabatic.

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Temperature Lapse Rates

Dry adiabatic lapse rate vs Wet adiabatic lapse rate


 The temperature decrease upon increase in altitude is less
for moist air than that for dry air
 The wet adiabatic lapse rate is not a constant, dependent on
altitude.
 In warm tropical air the wet adiabatic lapse rate is
approximately one-third of the dry adiabatic lapse rate

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Atmospheric Stability
The tendency of the atmosphere to resist or enhance vertical
motion is termed stability. It is related to both wind speed and
the change of air temperature with height (lapse rate).
A comparison of the adiabatic lapse rate with the environmental lapse
rate gives an idea of the stability of the atmosphere.

If an air parcel is displaced from its original height it can:


Return to its original height - Stable
Accelerate upward because it is buoyant - Unstable
Stay at the place to which it was displaced
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Atmospheric Stability (Neutral)

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Atmospheric Stability (Unstable)

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Atmospheric Stability (stable)

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Atmospheric Stability
Match it to text!!

Absolute instability
If the environmental lapse rate is greater
than the dry adiabatic lapse rate
Absolute stability
If the environmental lapse rate is less
than the wet adiabatic lapse rate
Conditional stability
If the environmental lapse rate is
between the dry adiabatic lapse rate
and wet adiabatic lapse rate

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Atmospheric Stability

Inversion
The extreme case of a stable
atmosphere, called an
inversion, occurs when
temperature increases with
altitude. Such a lapse rate is
known as negative lapse rate.
Under these conditions, the
atmosphere is very stable and
practically no mixing of
pollutants takes place

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Different Temperature Lapse


Rates

DALR : Dry Adiabatic Lapse Rate

WALR: Wet Adiabatic Lapse Rate

SALR: Super Adiabatic Lapse Rate

CS: Conditional Stability

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Problem
Following observations have been made for the temperature of the
atmosphere with respect to elevation to find the stability of the
atmosphere:

Is the atmosphere?

a. Stable
b. Unstable
c. Neutral
d. Extremely stable

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Problem 2

 A rising plume of stack gas has a temperature of 10000C


at 200m. Assuming a dry adiabatic lapse rate determine
the temperature at 800m

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Plume Behaviour
1. Coning Plume :
• Formed when horizontal wind velocity exceeds 32 km/h and
cloud blocks solar radiation during the day and terrestrial
radiation during the night.
• There is little vertical mixing.
• The environment is slightly stable under sub-adiabatic
conditions (WALR<ELR<ALR).
• The plume shape is vertically symmetrical about the plume
line.

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Plume Behaviour
2. Fanning Plume
• Formed at extreme inversion conditions owing to a negative lapse
rate.
• When the environment is under conditions of inversion, a stable
environment occurs just above the stack, and the plume moves
horizontally rather than upwards.
• Occurs more frequently when there is less turbulence.
• For high stack, fanning is considered a favorable meteorological
condition as it doesn’t cause ground pollution.

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Plume Behaviour
3. Looping Plume
• The wavy looping plume arises in a super-adiabatic environment
(ELR>>ALR), resulting in a very unstable atmosphere due to rapid
mixing.
• In an unstable atmosphere, rapid vertical air motions occur both
upward and downward, resulting in a looping plume.
• As a result, large pollution concentrations may arise near the
ground.
• It is preferable to create high stacks where the environment is
normally hyper adiabatic to scatter these contaminants.

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Plume Behaviour

4. Neutral Plume
• In neutral atmospheric circumstances (ELR=ALR), a
neutral plume forms.
• A neutral plume rises vertically in an upward direction.
• The plume will continue to rise until it reaches a height
where the density and temperature of the surrounding air
are equal.

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Plume Behaviour
5. Lofting Plume
• Lofting plume is produced by a strong super adiabatic lapse
rate immediately above the stack and a negative lapse
rate (inversion) immediately below the stack opening.
• The downward movement is stopped by inversion.
• This results in a very rapid and turbulent upward mixing of the
plume. But the downward mixing is less.
• As a result, the dispersion of pollutants becomes quick, and
pollutants cannot come down to the ground.
• Such a plume is good for dispersing air contaminants and
providing significant protection to living beings.

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Plume Behaviour
6. Fumigating Plume
• The fumigant plume is the exact opposite of the lofting plume.
• Formed when there is a negative lapse rate (inversion) just above
the stack and a strong super adiabatic lapse rate below the stack.
• Pollutants cannot escape above the stack under these conditions,
thus they settle towards the ground due to turbulence and mixing.
• As a result, the dispersion of contaminants in a fumigant plume is
exceedingly poor.

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Plume Behaviour

7. Trapping Plume
• When an inversion layer exists above and below the stack, the
plume does not rise or fall.
• Rather, it is constrained or trapped between the two inversion
levels, resulting in a trapping plume.
• This plume isn’t optimal for pollution dispersion since it can’t go
past a particular height.

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Identify the Plume Behavior

a b

c d

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Answer

a. Lofting or coning
b. Nuetral
c. Fumigating
d. Looping

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Wind Velocity and Turbulence


Differential solar heating of the Earth’s surface produces pressure and
temperature gradient. As a result, the atmosphere is practically in
continuous motion with air movements being always turbulent.
Thermal Turbulence: The motion of air near the surface of the Earth is
retarded by friction, which varies with surface roughness. The
planetary boundary layer, in which friction is significant, extends to
about 1 km above the Earth’s surface. The wind velocity profile
within the layer is not only influenced by the surface roughness but
also by the time of day. During the day, solar heating causes
thermal turbulence or eddies and these eddies set up convective
currents so that turbulent mixing is increased. This results in a more
flat velocity profile in the day than that at night.
Thermal turbulence also depends on the thermal stability of the
atmosphere. It is maximum on a clear sunny day in the afternoon
and minimum at night or in the early morning.

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Wind Velocity and Turbulence

Wind Velocity profiles during


day and night

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Wind Velocity and Turbulence


Mechanical Turbulence:
Is produced by shearing stress generated by air movement over the Earth’s surface-
the greater the surface roughness, the greater the turbulence. For smooth surfaces,
the air velocity profile becomes very steep near the ground. For rougher surfaces such
as those in urban areas more mechanical turbulence is generated and the velocity
profile becomes less steep and reaches deeper into the atmosphere
The mean wind speed variation with altitude in the planetary boundary layer can be
represented by a simple empirical power law such as,

p
u z
 
u1  z1 

Where u is the wind speed at altitude z, u1 is the wind speed at altitude z1 and the exponent
p varies between 0.07 and 0.55 depending on the roughness of the ground surface as well as
on the temperature stability of the atmosphere. The exponent α is observed to increase with
increasing stability or with increasing surface roughness.
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Wind Velocity and Turbulence


Effect of terrain roughness on the wind-speed profile
Values along curves represent percentages of gradient wind value

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Air quality modeling


 Air pollution modeling is a numerical tool used to describe
the causal relationship between emissions, meteorology,
atmospheric concentrations, deposition, and other factors.
 Air pollution measurements give important, quantitative
information about ambient concentrations and deposition,
but they can only describe air quality at specific locations
and times, without giving clear guidance on the
identification of the causes of the air quality problem.
 Air pollution modeling, instead, can give a more
complete deterministic description of the air quality
problem, including an analysis of factors and causes
(emission sources, meteorological processes, and physical
and chemical changes), and some guidance on the
implementation of mitigation measures.
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Air quality modeling

• A mathematical relationship between emissions and air


quality that incorporates the transport, dispersion and
transformation of compounds emitted to air
• The models are useful tools in design of new, large or
otherwise modification of existing processes
Unsteady state: box
grid
spectral
puff
trajectory
Steady state: Gaussian

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Dispersion of air pollutants


(Gaussian plume model)
 Determine emission and stack parameters
 Estimate pollutant concentration
 Determine plume rise
Assumptions:
 Diffusion negligible in the downwind direction
 Constant emission rate
 Uniform atmospheric stability throughout the layer into
which the contaminated gas stream is discharged

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Gaussian plume model


The plume spreads as it moves in the x direction such that the local
concentrations ρ(x,y,z) (kg/m3 ) at any point in space form
distributions which have shapes that are “Gaussian” or “normal” in
planes normal to the x direction.

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Gaussian plume model

Q = rate of pollutant emission (available or determined from process


conditions) (kg/s)
x, y, z values correspond to the location where pollutant
concentration is to be estimated downwind from the source
ū = average wind speed at the stack height H
σy, σz= Spreading coefficients/diffusion coefficients
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ETZC362/PEZC411
Prof. Krishna C. Etika
Associate Professor
BITS Pilani Department of Chemical Engineering
Pilani Campus B.I.T.S-Pilani, Pilani Campus

ETZC362/PEZC411 Environmental Pollution Control

Meteorological Aspects of Air


Pollutant Dispersion

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Identify the Plume Behavior

a b

c d

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Answer

a. Lofting or coning
b. Nuetral
c. Fumigating
d. Looping

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Wind Velocity and Turbulence


Mechanical Turbulence:
Is produced by shearing stress generated by air movement over the Earth’s surface-
the greater the surface roughness, the greater the turbulence. For smooth surfaces,
the air velocity profile becomes very steep near the ground. For rougher surfaces such
as those in urban areas more mechanical turbulence is generated and the velocity
profile becomes less steep and reaches deeper into the atmosphere
The mean wind speed variation with altitude in the planetary boundary layer can be
represented by a simple empirical power law such as,

p
u z
 
u1  z1 

Where u is the wind speed at altitude z, u1 is the wind speed at altitude z1 and the exponent
p varies between 0.07 and 0.55 depending on the roughness of the ground surface as well as
on the temperature stability of the atmosphere. The exponent α is observed to increase with
increasing stability or with increasing surface roughness.
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Wind Velocity and Turbulence


Effect of terrain roughness on the wind-speed profile
Values along curves represent percentages of gradient wind value

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Air quality modeling


 Air pollution modeling is a numerical tool used to describe
the causal relationship between emissions, meteorology,
atmospheric concentrations, deposition, and other factors.
 Air pollution measurements give important, quantitative
information about ambient concentrations and deposition,
but they can only describe air quality at specific locations
and times, without giving clear guidance on the
identification of the causes of the air quality problem.
 Air pollution modeling, instead, can give a more
complete deterministic description of the air quality
problem, including an analysis of factors and causes
(emission sources, meteorological processes, and physical
and chemical changes), and some guidance on the
implementation of mitigation measures.
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ETZC362/PEZC411 Environmental Pollution Control

Air quality modeling

• A mathematical relationship between emissions and air


quality that incorporates the transport, dispersion and
transformation of compounds emitted to air
• The models are useful tools in design of new, large or
otherwise modification of existing processes
Unsteady state: box
grid
spectral
puff
trajectory
Steady state: Gaussian

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Dispersion of air pollutants


(Gaussian plume model)
 Determine emission and stack parameters
 Estimate pollutant concentration
 Determine plume rise
Assumptions:
 Diffusion negligible in the downwind direction
 Constant emission rate
 Uniform atmospheric stability throughout the layer into
which the contaminated gas stream is discharged

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Gaussian plume model


The plume spreads as it moves in the x direction such that the local
concentrations ρ(x,y,z) (kg/m3 ) at any point in space form
distributions which have shapes that are “Gaussian” or “normal” in
planes normal to the x direction.

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Gaussian plume model

Q = rate of pollutant emission (available or determined from process


conditions) (kg/s)
x, y, z values correspond to the location where pollutant
concentration is to be estimated downwind from the source
ū = average wind speed at the stack height H
σy, σz= Spreading coefficients/diffusion coefficients
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Gaussian Plume Model –


Ground Level Concentration

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Gaussian Plume Model –


Ground Level Concentration

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Gaussian Plume Model –


Ground Level Concentration

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Gaussian Plume Model –


Estimation of σy and σz

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Gaussian Plume Model –


Estimation of σy and σz
Pasquill and Gifford’s Method

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Gaussian Plume Model –


Estimation of σy and σz
Curves of Pasquill -Gifford

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Gaussian Plume Model –


Estimation of σy and σz
Limitation of Pasquill-Gifford Method
(1) The estimated concentration from these charts or
equations corresponds to a sampling time of 10 min
(2) Underestimates the plume dispersion in urban areas
(3) Uncertainties increase with increasing distance from
source

For sampling time other than 10 min,

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Limitation of Gaussian Plume


Model
(1) Most accurate for distance of 100 to 2000 meters.
(2) Neglects the wind turning effect arising due to friction.
(3) Ignores absorption and desorption of pollutants
(4) Ignores reactive pollutants.

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Problem
A chimney with a design stack height of 250 m is emitting
Sulphur dioxide at a rate of 500 g/s on a sunny day in
June with moderate wind speed (6 m/s) at stack altitude.
Estimate the SO2 concentration at (1000, 50, 0, 250)
[p=0.25]

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Effective Stack Height

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Effective Stack Height


The value for the effective stack height is the sum of the
physical stack height'(H) and the plume rise (∆H)

Heff = H + ∆H

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AIR POLLUTION CONTROL


METHODS

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CONTROL METHODS

Prevent or Minimize
• Source Correction
• Raw Material Changes
• Process Changes
• Equipment Modification or Replacement
• Effluent Treatment
• Particulate control
• Gases and odors control
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PARTICULATE EMISSION
CONTROL
Particle sizes range generally from 100 μm
down to 0.1 μm and even less
Factors to be considered
– Physical and Chemical characteristics
– Size and Concentration
– Volume to be handled
– Temperature and Humidity
– Toxicity and Inflammability

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COLLECTION EFFICIENCY
Represents system performance

Weight , collected
Gravimetric efficiency T 
Total , entering

fraction in range i collected


Fractional efficiency i  100
mi
n

 m i i

Overall efficiency T  i 1
percent
M

mi= amount in range ‘i’ entering the collector


M= Total amount entering the collector

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Example
An air pollution control device removes a particulate that is being
emitted at a concentration of 125,000μg/m3 at an air flow rate of 180
m3/sec. What is the concentration of the emission and the efficiency of
collection? The device removes 0.48 metric tons per day.
Feed Escaped
Pollution control
device
x0  x2
Removed
At steady state the mass balance is: x1
Rate of particulates in = rate of particulates out
Rate of particles in = rate of particles removed + rate of particles escaping
180 m3/sec x 125,000 g/m3 x 10-6 g/g = 22.5 g/sec

Particles collected:
0.48 tons/day x 106 g/ton x 1 hr/3600 sec x 1 day/24 hr = 5.5 g/sec
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Example

Mass balance:

22.5 = 5.5 + particles that escape

Particles that escape = 17 g/sec

Emission concentration:
(17 g/sec x 106 g/g)/ 180 m3/sec = 94,000 g/m3

Recovery:

R = (x1 x 100)/x0 = (5.5 x 100)/22.5 = 24%

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PARTICULATE CONTROL
EQUIPMENT
• Gravitational settling
• Settling chambers
• Centrifugal impaction
• Cyclone separators
• Inertial impaction
• Direct interception
• Fabric filters
• Diffusion
• Scrubbers
• Electro-static precipitation
• ESP

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Particle range for different


types of equipments

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Gravitational Settling Chamber


Generally used to remove large, abrasive particles (>50μm)
Advantages:
 Low pressure drop
 Require simple maintenance
Disadvantages:
 Low efficiency for particles smaller than 50μm
These Devices are normally used as precleaners prior to passing the gas
stream through high efficiency collection devices.

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Gravitational Settling Chamber


Howard type settling chamber
 Several trays
 Efficiency improved
 Gas flow velocity constant but shorter settling distance.
Gas inlet
Gas outlet

ΔH
v
H

L
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Effect of Settling Chamber


Height

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Gravitational Settling Chamber


Howard type settling chamber
 Several trays
 Efficiency improved
 Gas flow velocity constant but shorter settling distance.
Gas inlet
Gas outlet

ΔH
v
H

L
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Gravitational Settling Chamber


Design Concepts
Area 2W  H
Hydraulic diameter Dh  4 
Perimeter W  H
vDh 
Reynolds Number Re 

Q
Velocity inside the chamber v
nW H W= width of each plate
Q= Vol. flow rate
2Q n= # of plates
So, Reynolds Number Re 
n [W  H ]
H
But the spacing between trays H  If the dust of Hd is already present, then
n
H
Therefore
2Q H   Hd
Re  n
[ nW  H  nH d ]
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Gravitational Settling Chamber


For laminar flow conditions (Re<2300) The time take by the air parcel
containing the particle to leave
the chamber
L
y L t
Time taken to settle, t  How? v
vt v
If the particle settles during this
time with velocity The
y
So, the collection efficiency,  distance, y travelled by particle is
H y= t
Lvt nWLvt
 
vH Q

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Gravitational Settling
Chambers

Performing Force Balance On the Settling Particle:

 1 
C D [ d p2 ][  g vt2 ]  d 3p [  p   g ]g
4 2 6

Then the terminal velocity is given by


For Stoke’s Law Region

4 gd p [  p   g ] gd p2 [  p   g ]
vt  
3C D  g 18 g

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Gravitational Settling Chamber

For Stokes law region, 24


CD  Rep<1
Re p
For turbulent region., C D  0.45 Rep>1000

For intermediate region.,

If the stokes law is applied, the minimum particle size that can be removed with 100%
efficiency is given by

18Q g
d p , min 
nWLg [  p   g ]

For turbulent flow, the equation for calculating the efficiency is Homework
nWLvt
  1  exp[ ] Derive this equation
Q 41
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Environmental Pollution Control


ETZC362/PEZC411
Prof. Krishna C. Etika
Associate Professor
BITS Pilani Department of Chemical Engineering
Pilani Campus B.I.T.S-Pilani, Pilani Campus

ETZC362/PEZC411 Environmental Pollution Control

AIR POLLUTION CONTROL


METHODS

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CONTROL METHODS

Prevent or Minimize
• Source Correction
• Raw Material Changes
• Process Changes
• Equipment Modification or Replacement
• Effluent Treatment
• Particulate control
• Gases and odors control
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Gravitational Settling Chamber


Howard type settling chamber
 Several trays
 Efficiency improved
 Gas flow velocity constant but shorter settling distance.
Gas inlet
Gas outlet

ΔH
v
H

L
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Gravitational Settling Chamber


Design Concepts
Area 2W  H
Hydraulic diameter Dh  4 
Perimeter W  H
vDh 
Reynolds Number Re 

Q
Velocity inside the chamber v
nW H W= width of each plate
Q= Vol. flow rate
2Q n= # of plates
So, Reynolds Number Re 
n [W  H ]
H
But the spacing between trays H  If the dust of Hd is already present, then
n
H
Therefore
2Q H   Hd
Re  n
[ nW  H  nH d ]
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Gravitational Settling Chamber


For laminar flow conditions (Re<2300) The time take by the air parcel
containing the particle to leave
the chamber
L
y L t
Time taken to settle, t  How? v
vt v
If the particle settles during this
y time with velocity The
So, the collection efficiency,  distance, y travelled by particle is
H y= t

Lv t nWLv t
 
vH Q

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Gravitational Settling
Chambers

Performing Force Balance On the Settling Particle:

 1 
C D [ d p2 ][  g vt2 ]  d 3p [  p   g ]g
4 2 6

Then the terminal velocity is given by


For Stoke’s Law Region

4 gd p [  p   g ] gd p2 [  p   g ]
vt  
3C D  g 18 g

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Gravitational Settling Chamber

For Stokes law region, 24


CD  Rep<1
Re p
For turbulent region., C D  0.45 Rep>1000

For intermediate region.,

If the stokes law is applied, the minimum particle size that can be removed with 100%
efficiency is given by

18Q g
d p , min 
nWLg [  p   g ]

For turbulent flow, the equation for calculating the efficiency is Homework
nWLvt
  1  exp[ ] Derive this equation
Q 8
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Deviations in Efficiency

Factors causing deviations in efficiency


 Hindered settling at high particle concentrations
 Non-uniform gas velocity over the settling height and width
 Particle re-entrainment
 Turbulence

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Gravitational Settling Chamber

Advantages Disadvantages
• Low capital cost • Large size
• Low energy cost • Low collection
• Low operating cost efficiency
• Low pressure drop • Trays in multi tray
chambers may warp

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Problem

A multi-tray settling chamber handles 6m3/s of air at 200C.


There are 8 trays including the bottom surface spaced
0.25m apart. The chamber is 4m long and 1 m wide. For
particles of density 2000 kg/m3 and for sizes 70 and 25 m,
calculate
• The residence time
• The distance settled
• Efficiency of collection

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Solution
Q L
v
nW H
t
v
4 gd p [  p   g ] 2Q
vt 
3C D  g Re 
n[W  H ]

y

H
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Cyclone Separators

Particulate laden gas is


accelerated through a
spiral motion which
imparts centrifugal
force to the particles

Particles are hurled out


of the spinning gas by
impact on the cylinder
wall of the cyclone
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Reverse Flow Cyclone


Separator

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Cyclone Separators

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Cyclone Separators

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Cyclone Design Considerations

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Cyclone Separation Factor, S

The magnitude of centrifugal force is frequently described


in terms of the number of times this force exceeds the
force of gravity, i.e, Separation factor, (S)

Where Vθ= Tangential particle velocity


r= radius of rotation

S varies from 5 in large, low velocity units to 2500 in small,


high pressure units

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Cyclone Separators

The tangential velocity of both particle and gas is same. By balancing


the radial drag force and the centrifugal force,
 v2
3 g d p v r  d 3p [  p   g ] 
6 r
From this,

d p2 [  p   g ]v2
vr 
18 g r

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Cyclone Separators
By experiments,
v r n  const
For ideal gas n=1
Vθ can be expressed in terms of Vθi , inlet tangential velocity of the gas
D n Q
v  vi [ ] v i 
2r Ai
d p2 [  p   g ] Q 2 D 2 n 1
vr  { } [ ] [ 2 n 1]
18 g Ai 2 r
Where, Q= gas volumetric flow rate, D= Diameter of cyclone
 As the radial velocity increases, the efficiency also increases, But at the cost of some
pressure drop.

Cut Size (dpc)


Which is the size of those particles that are collected with 50% efficiency. Particles
larger than dpc will have a collection efficiency greater than 50% while the smaller
particles will be collected with lesser efficiency
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Efficiency of Cyclone Separators


Most Satisfactory expression for cyclone performance is Empirical. Efficiency of collection
determined from an empirical expression and Lapple’s correlation chart

dpc=

Where, b= inlet width,


vi= gas inlet velocity,
Ne= effective number of turns a gas makes in
traversing the cyclone (5-10 in most cases)

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Example (Cyclone)
Determine the cut size diameter of a cyclone for the
following data

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Cyclone Separators –
Pressure Drop
∆P =

K = a constant which averages 13 and ranges from 7.5 to 18.4


∆P = pressure drop
a, b, De = cyclone dimensions
νi = inlet gas velocity
ρg = gas density

 Pressure drop is proportional to inlet velocity in squares.


 This influences the economy and efficiency of the
cyclone separator
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Cyclone Separators

As diameter decreases, efficiency increases


However, pressure drop also increases

Cyclones are efficient for particles larger than 10 µm

Uses
• Sawmill
• Oil refinery
• Cement plant

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Filters

• Removal of particles less than 5 m


Two types
• Deep bed filter (Packed filter)
• A packing of fibers is used to intercept the particles in the gas stream
• Used for low volume and relatively clean gas (air conditioning system)

• Fabric (Bag) Filter


• For dirty industrial gas

• Mechanism involved are


• Inertial Impaction
• Direct interception
• Diffusion

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FABRIC/BAG FILTERS
Operation
 Consists of a tubular bag or an envelope
 Particle laden gas enters the bag at the bottom
 Passes through the fabric
 Particles will deposit on the fabric, in side the bag
 As particulate matter collects on the bag, collection efficiency
increases
 At some point the pressure drop across the bag reduces the
gas flow rate to an unacceptable level.
 Cleaning is done in a time interval
 Three methods of cleaning  mechanical shaking, reverse
air flow, pulse jet
 Some times the reverse pressure drop is also used

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Bag Filter

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Packed Filters

INERTIAL IMPACTION

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Packed Filters
INTERCEPTION

Interception and impaction usually account for 99% of the


collection of particles larger than 1 μm
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Packed Filters

DIFFUSION (Electrostatic attraction)

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Packed Filters

INERTIAL IMPACTION
2𝑦𝑜
∅𝑐 =
𝑑𝑓
𝜙𝑐= Collision Factor
𝜙𝑎= Adherence Factor

𝜂𝑖𝑚𝑝𝑎𝑐𝑡 = 𝜙𝑐𝜙𝑎

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Packed Filters
Interception and impaction usually account for 99% of the
collection of particles larger than 1 μm
INTERCEPTION

For Potential Flow

𝜂𝑖𝑛𝑡𝑒𝑟 = 1 + −

Potential flow is an idealized model of fluid flow that occurs in the


case of incompressible, inviscid, and irrotational flow.

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Packed Filters

DIFFUSION (Electrostatic attraction)

.
𝐶𝐷𝑓𝑅𝑒𝑓 .
𝜂𝑑𝑖𝑓𝑓𝑢𝑠𝑖𝑜𝑛 = 0.775
𝑃𝑒
2
CDf= Drag coefficient of the fiber
Ref = Reynolds number based on fiber diameter
Pe = Peclet number
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Combined Efficiency of
Collection
In practice, the collection mechanisms of impaction,
interception and diffusion are not independent.

A reasonable estimate for combined efficiency of collection


is,

𝜂𝑓 = 1 − (1 − 𝜂𝑖𝑚𝑝𝑎𝑐𝑡)(1 − 𝜂𝑖𝑛𝑡𝑒𝑟)(1 − 𝜂𝑑𝑖𝑓𝑓𝑢𝑠𝑖𝑜𝑛)

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Bag Filters

Advantages
Very high efficiencies
Retention of finest particles
Collection of particles in dry form
Lesser pressure drop
Disadvantages
Large size
High construction costs
Their application only to process temperature < 285 0C

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SPRAY TOWERS

Operation
 Water is introduced by means of spray nozzles
 The polluted gas flow upwards and the particle collection
results because of inertial impaction and interception on the
droplet
 The maximum collection efficiency by inertial impaction has
been found to be independent of particle size
Efficiency - a complex function of
 Droplet size
 Flow velocity of gas
 Liquid:gas ratio
 Droplet trajectories

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SPRAY TOWERS

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SPRAY TOWERS
For identical spherical droplets falling through a slow upward moving gas stream , the overall
collection efficiency is given by

 sc  1  (1  d ) n

Where, n = number of collecting droplets encountered by a group of particles and ηd =


individual drop collection efficiency
For spray towers the value of n can be calculated from the expression

1.5m s L  1 1 
n   
 L d  Q Asc (v td  v p ) 

Where, ms= mass flow rate of spray liquid, L=height of spray tower, d = average droplet size,
Q = volumetric flow rate of gas, ρL= spray liquid density, Asc= tower cross-sectional area, vtd
= terminal free falling velocity of the droplet, and vp= particle velocity
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CENTRIFUGAL SCRUBBERS

 The collection efficiency for particles smaller than those


recovered in spray towers can be increased

 The simplest type of centrifugal scrubber can be


constructed by inserting banks of nozzles inside a
conventional dry cyclone

 In the absence of spray the efficiency will be the same as


that for the dry collector

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CENTRIFUGAL SCRUBBERS
Operation
 The polluted gas introduced tangentially into the
lower portion of the vertical cylinder
 Water drops are injected into the flow stream from
sprays directed outward from a central manifold
 These droplets are caught in the spinning gas
stream and are thrown upward toward the wall by
centrifugal force
 During their motion, the droplets collide with the
particles and capture them
 The scrubbing liquid along with the particles flows
down the wall to the bottom of the scrubber
 The cleaned gas exits through a demister and is
processed for the removal of any entrained water
droplets
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PACKED BEDS AND PLATE


COLUMNS
 In a typical countercurrent-flow packed scrubber the polluted
gas stream moves upward and comes in contact with the
scrubbing liquid stream which is moving downward over the
packing in a film
 The packing provides a target, which allows the gas stream
to take a curved path through the pore spaces while the
particles carried by the gas stream are captured by inertial
impaction
 Collection of particles by diffusion is also possible
 Smaller packing increases the efficiency of collection but its
shape does not appear to affect the collection efficiency
 Packed tower can be chosen for scrubbing particles that are
soluble in the scrubbing liquid; otherwise, the packing will
encounter plugging problems

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PACKED BEDS AND PLATE


COLUMNS

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Venturi Scrubber
 Venturi scrubbers offer high performance collection of fine particles,
usually smaller than 2 to 3 μm in diameter
 These scrubbers are suitable for sticky, flammable, or high
corrosive particulate matter
 The high performance of the venturi scrubbers is achieved by
accelerating the gas stream to very high velocities, of the order of
60-120 m/s
Operation
 The droplets accelerate in the throat section and due to the velocity
difference between the particles and the droplets the particles are
impacted against the slow-moving droplets
 The gas liquid mixture is then directed to a separation device such
as a cyclone separator where the droplets carrying the particulate
matter are separated from the gas stream

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Venturi Scrubber

Mechanisms involved
 Inertial impaction
 Diffusion
 Electrostatic-phenomenon
 Condensation
 Agglomeration

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Venturi Scrubber
Johnstone et al. correlated the collection efficiency of the venturi scrubber with the
impaction parameter (ψ) as:

  1  exp( KR  )

K = Correlation factor= f(throat geometry)


R = Liquid flow rate /m3 of gas
 = inertial impaction parameter  relates the particle and droplet sizes and relative
velocities Cρ p v r (d p ) 2
ψ C= Cunningham correction factor
18d d 
The diameter of the droplet (dd) obtained from gas atomization in the venturi throat can be
evaluated from the following equation:
16400
dd   1.45L1.5
vr
Where, dd is in μm, L is the liquid flow rate (gal/1000 ft3 of gas), and vr is the relative velocity
of gas to liquid at venturi throat in ft/sec
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Problem

Calculate the venturi throat area required to achieve 99%


removal of 1.25 m radius particle having a density of
1400 kg/m3 for the following gas stream and venturi
characteristics
Gas flow rate – 10 m3/s
Gas temp – 1800C
Droplet diameter – 100 m
Liquid flow rate – 0.1 m3/s
Coefficient k = 200

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Environmental Pollution Control


ETZC362/PEZC411
Prof. Krishna C. Etika
Associate Professor
BITS Pilani Department of Chemical Engineering
Pilani Campus B.I.T.S-Pilani, Pilani Campus

ETZC362/PEZC411 Environmental Pollution Control

AIR POLLUTION CONTROL


METHODS

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Electrostatic Precipitator

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Electrostatic Precipitators

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Collection Efficiency- ESP

If electric field strength is Ec is present, a force Fel will act on it


such that
Fel = qpEc

An opposite drag force, FD, resists Fel. When the net force is 0,
particles moves with constant drift velocity, Vm

Fel = FD
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Collection Efficiency - ESP

The Cunningham correction factor or Cunningham slip correction factor is used to account
for non-continuum effects when calculating the drag on small particles. The derivation
of Stokes' law, which is used to calculate the drag force on small particles, assumes a no-slip
condition which is no longer correct at high Knudsen number

https://www.youtube.com/watch?v=y_ONwi7hauc

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Collection Efficiency-ESP

For stoke law region

νpm = Constant drift velocity of particle

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Collection Efficiency- ESP

Q,v
c(z) c(z+ΔZ)

ΔZ

Mass Balance Qc(z) = Qc(z+ΔZ) + c(z)vpmP ΔZ

At Z=0, C=Co
At Z=L, C = CL
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Collection Efficiency - ESP

But PL = Ac ( Lateral Surface Area of Collector)

Q=A*v = (V/L)*v

V= Volume of Precipitator
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Collection Efficiency- ESP

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Problem

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Electrostatic Precipitators
Advantages

Low Pressure drop, power requirement is small compared to that in other devices
economical and simple to operate
99+ percent efficiency obtainable very small particles can be collected wet or dry
Can Handle both gases and mists for high volume flow
Operated at high temperatures and pressures.
Few moving parts
Disadvantages
Relatively high initial cost and large space
Sensitive to variable particulate loadings or flow rates
Safe guard of operating personnel from high voltage is necessary
Collection efficiency can deteriorate gradually

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Venturi Scrubber
 Venturi scrubbers offer high performance collection of fine particles,
usually smaller than 2 to 3 μm in diameter
 These scrubbers are suitable for sticky, flammable, or high
corrosive particulate matter
 The high performance of the venturi scrubbers is achieved by
accelerating the gas stream to very high velocities, of the order of
60-120 m/s
Operation
 The droplets accelerate in the throat section and due to the velocity
difference between the particles and the droplets the particles are
impacted against the slow-moving droplets
 The gas liquid mixture is then directed to a separation device such
as a cyclone separator where the droplets carrying the particulate
matter are separated from the gas stream

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Venturi Scrubber

Mechanisms involved
 Inertial impaction
 Diffusion
 Electrostatic-phenomenon
 Condensation
 Agglomeration

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Venturi Scrubber
Johnstone et al. correlated the collection efficiency of the venturi scrubber with the
impaction parameter (ψ) as:

  1  exp( KR  )

K = Correlation factor= f(throat geometry)


R = Liquid flow rate /m3 of gas
 = inertial impaction parameter  relates the particle and droplet sizes and relative
velocities Cρ p v r (d p ) 2
ψ C= Cunningham correction factor
18d d 
The diameter of the droplet (dd) obtained from gas atomization in the venturi throat can be
evaluated from the following equation:
16400
dd   1.45L1.5
vr
Where, dd is in μm, L is the liquid flow rate (gal/1000 ft3 of gas), and vr is the relative velocity
of gas to liquid at venturi throat in ft/sec
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Problem

Calculate the venturi throat area required to achieve 99%


removal of 1.25 m radius particle having a density of
1400 kg/m3 for the following gas stream and venturi
characteristics
Gas flow rate – 10 m3/s
Gas temp – 1800C
Droplet diameter – 100 m
Liquid flow rate – 0.1 m3/s
Coefficient k = 200

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Problem

Calculate the venturi throat area required to achieve 99%


removal of 1.25 m radius particle having a density of
1400 kg/m3 for the following gas stream and venturi
characteristics
Gas flow rate – 10 m3/s
Gas temp – 1800C
Droplet diameter – 100 m
Liquid flow rate – 0.1 m3/s
Coefficient k = 200

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Selection of a particulate
collector
The selection of a suitable control device for a specific
application requires consideration of
 Particle size
 Concentration of particles
 Desired efficiency of collection
 Costs
 Space available
 Maintenance factors
Figure gives the efficiencies of various gas cleaning devices for
three broad particulate size categories
 Coarse
 Fine
 Superfine dusts
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Selection of a particulate
collector
A) Settling Chamber
B) Simple Cyclone
C) High-efficiency
Cyclone
D) Electrostatic
Precipitator
E) Spray Tower wet
scrubber
F) Venturi Scrubber
G) Bag Filter

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Use of particulate collectors in


industry
Industry or process Particulate matter Collection devices
Steel Iron oxide, dust, smoke Cyclones, fabric filters,
electrostatic precipitators, wet
scrubbers
Metallurgical (non-ferrous) Smoke, metal fumes, fabric filters, electrostatic
oil, grease precipitators, wet scrubbers
Cement, Phosphate, gypsum, Process dusts fabric filters, electrostatic
alumina processing precipitators, wet scrubbers,
mechanical collectors
Kraft paper mills Chemical dusts electrostatic precipitators, venturi
scrubbers
Sulphuric, phosphoric, nitric acid Acid mist, dust electrostatic precipitators, mesh
manufacture mist eliminators
Petroleum refineries Catalyst dust, ash from High-efficiency cyclones,
sludge electrostatic precipitators,
scrubbing towers
Power generation Coal dust, fly ash Mechanical collectors,
electrostatic precipitators
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CONTROL OF GASEOUS
EMISSIONS
There are essentially two classes of techniques by which
gaseous pollutants may be removed from an effluent stream
1. Sorption of pollutant, through absorption in a liquid or
adsorption on a solid surface
2. Chemical alteration of the pollutant, usually through
combustion or catalytic treatment
Absorption by Liquids
 Three steps: diffusion to interface  transfer across interface
 diffusion into liquid
 A two film resistance theory, initially suggested by Whitman,
is often used to explain this process
 According to the theory, the interface offers no resistance to
mass transfer, and the mass transfer rate between the two
phases is controlled by the rates of diffusion through the
phases on each side of the interface

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CONTROL OF GASEOUS
EMISSIONS
Direction of mass transfer
Concentration of component A

Gas Liquid
phase phase
CAi
PAG

CAL
PAi

Interface

Distance, z

Concentration Profiles
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CONTROL OF GASEOUS
EMISSIONS
For dilute solutions the equilibrium relation between pA and
CA can be expressed in terms of Henry’s law
p A  HC A
Where, H is the Henry’s constant, which depends on the
definition of concentration units. If the Henry’s law is
expressed in terms of mole fraction, then

pA  H ' xA
Smaller values of H’ represents higher solubility of the gas

What is the difference between Rault’s Law and Henry’s


Law?

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Henry’s Vs Rault’s Law

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Absorption
The effectiveness of an absorption process for air pollution
control mostly depends on the selection of a suitable
scrubbing medium
Important properties of solvents for industrial applications
are:
 High gas solubility and high selectivity between solute
species
 Low vapour pressure
 Non-corrosiveness
 Easy regeneration and recovery
 Low costs
 Low viscosity at absorption temperature
 Nontoxicity
 Nonflammability
 Chemical stability

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Absorption
Gas Absorption Equipment
Gas absorption is commonly conducted in equipment which are
designed to provide intimate contact between the two phases
Commonly used absorbers
 Packed towers
 Plate and spray towers
 Venturi scrubbers

In air pollution control, the most popular means of gas cleaning


is the packed tower; however, tray columns, spray and
venturi scrubbers are used in nearly 10% of the cases.

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PACKED BEDS AND PLATE


COLUMNS

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Types of Packings

Metal pall ring Plastic Super Intalox Saddle Raschig Rings

Lessing Ring Partition Ring


Berl Saddle
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Types of Tray

Sieve Tray
Bubble Cap

17 September 2023 Valve Tray 29


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Absorption- Basic Design


Consideration
Consider a steady-state operation involving a countercurrent absorber
as shown in figure

Three variables of interest in the design Ls Gs


of a packed tower are: G2 G2
1. gas flow rate, x2 y2
X2 Y2 L = Total liquid flow rate/area
2. liquid flow rate
G = Total gas flow rate/area
3. height of tower. Plane2
y = mole fraction of solute
in GAS phase
For height dZ, the total interfacial dz x = mole fraction of solute
area open to mass transfer is: in LIQUID phase
Y = mole ratio of solute in
z GAS phase
a*V = a*(AdZ)
Plane1 X= mole ratio of solute in
Ls Gs LIQUID phase
a= interfacial area/ tower volume
A = Tower cross-sectional area L1 G1
X1 y1
X1 Y1
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Environmental Pollution Control


ETZC362/PEZC411
Prof. Krishna C. Etika
Associate Professor
BITS Pilani Department of Chemical Engineering
Pilani Campus B.I.T.S-Pilani, Pilani Campus

ETZC362/PEZC411 Environmental Pollution Control

AIR POLLUTION CONTROL


METHODS

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Absorption
The effectiveness of an absorption process for air pollution
control mostly depends on the selection of a suitable
scrubbing medium
Important properties of solvents for industrial applications
are:
 High gas solubility and high selectivity between solute
species
 Low vapour pressure
 Non-corrosiveness
 Easy regeneration and recovery
 Low costs
 Low viscosity at absorption temperature
 Nontoxicity
 Nonflammability
 Chemical stability

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Absorption
Gas Absorption Equipment
Gas absorption is commonly conducted in equipment which are
designed to provide intimate contact between the two phases
Commonly used absorbers
 Packed towers
 Plate and spray towers
 Venturi scrubbers

In air pollution control, the most popular means of gas cleaning


is the packed tower; however, tray columns, spray and
venturi scrubbers are used in nearly 10% of the cases.

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PACKED BEDS AND PLATE


COLUMNS

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Types of Packings

Metal pall ring Plastic Super Intalox Saddle Raschig Rings

Lessing Ring Partition Ring


Berl Saddle
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Types of Tray

Sieve Tray
Bubble Cap

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Absorption
Two Film Theory: The rate of mass transfer of solute NA per unit interfacial
area from the gas phase and across the interface must equal to that in the
liquid phase, i. e.,
N A  kG ( pG  pi )  k L (ci  cL )

It is impossible to know the A


pG C
interface partial pressures
and concentrations  the rate
equations are normally Equilibrium
expressed in terms of overall pi B curve
coefficient (i.e., KG &KL) D
based on an overall driving p*
force between the bulk
compositions, pG and cL.
These are defined by
cL ci c*
N A  K G ( pG  p  )  K L (c   cL ) The driving force in gas absorption
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Absorption
Above equations in terms of mole fractions
N A  kG ( yG  yi )  k L ( xi  xL )
N A  K G ( yG  y  )  K L ( x   x L )
And equilibrium relationship in terms of mole fractions yi  mxi
Where, m = H’/P, and P = total pressure
Relation between overall mass transfer coefficient and individual mass transfer
coefficient

1 1 m
 
K y ky kx

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Absorption- Basic Design


Consideration
Consider a steady-state operation involving a countercurrent absorber
as shown in figure

Three variables of interest in the design Ls Gs


of a packed tower are: G2 G2
1. gas flow rate, x2 y2
X2 Y2 L = Total liquid flow rate/area
2. liquid flow rate
G = Total gas flow rate/area
3. height of tower. Plane2
y = mole fraction of solute
in GAS phase
For height dZ, the total interfacial dz x = mole fraction of solute
area open to mass transfer is: in LIQUID phase
Y = mole ratio of solute in
z GAS phase
a*V = a*(AdZ)
Plane1 X= mole ratio of solute in
Ls Gs LIQUID phase
a= interfacial area/ tower volume
A = Tower cross-sectional area L1 G1
X1 y1
X1 Y1
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Absorption- Basic Design


Consideration
A solute material balance gives G1 y1  L2 x 2  G 2 y 2  L1 x1
Since G and L vary along the height of the tower, it is much simpler to express
material balance equations in terms of solute-free concentration units. Then
material balance equation becomes
Gs (Y1  Y2 )  Ls ( X 1  X 2 )
Where, Gs= molal flow rate of non-diffusing material (i.e., solvent) in gas phase/cross
sectional area of tower, Ls = molal flow rate of non diffusing material (i.e., solvent) in
liquid phase/cross sectional area of tower,
The equation for the operating line with slope

Ls Y  Y2
 1
Gs X 1  X 2
In general form, the operating line equation may be represented as
L 
Y  Y1   s ( X 1  X )
1 October 2023
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Absorption- Basic Design


Consideration
X1, Y1
Operating line

Ls
slope 
Gs Equilibrium Curve
Y
Yi  f ( X i )

X2, Y2

X
Equilibrium and operating lines in a countercurrent tower
A solute material balance over the differential length dz

L 
d (Y )  d {Y1   s ( X 1  X )}  GsdY  LsdX
 Gs  12
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Absorption- Basic Design


Consideration
Now, for a differential section of the tower with height dz and
interfacial are dA, the rate of absorption is
Ls Gs
G2 G2
x2 y2
N A dA  K y ( y  y  )dA X2 Y2
Plane2
But , dA  aAdz
 N A adz  K y a ( y  y  )dz dz

z
For height dZ, the total interfacial area open to mass
transfer is: Plane1
Ls Gs
L1 G1
a*V = a*(AdZ)
X1 y1
X1 Y1
a= interfacial area/ tower volume, A = Tower cross-
sectional area
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Absorption- Basic Design


Consideration
 G s dY  K y a ( y  y * )dz
 y  dy
G s dY  G (1  y)d   G
 1  y  1 y
dy
G  K y a ( y  y * )dz
1 y

Multiplying and dividing the right hand side of above equation by


(1-y)lm and assuming that the product of this and Kya is a constant, we
can integrate for the height of the tower Z
y1
G (1  y ) lm dy
Z
K y a (1  y )lm  (1  y)( y  y )
y2
*

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Absorption- Basic Design


Consideration

HOG = Height of Overall Transfer Unit based on gas side

y1
G (1  y )lm dy
Z
K y a (1  y ) lm  (1  y)( y  y )  H
y2
* OG N OG

NOG = # of Overall Transfer Unit required to achieve separation from


y1y2

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Absorption- Basic Design


Consideration
If the two contacting systems are relatively dilute, and both the
operating and equilibrium lines are straight over the tower
height, then it can be shown that

y1  y 2
N OG 
[ y  y * ]lm
Where ,
[ y  y * ]1  [ y  y * ] 2
[ y  y * ]lm 
[ y  y * ]1
ln
[ y  y * ]2

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Absorption- Basic Design


Consideration
HOG may be estimated from individual phase transfer unit heights according to the relation

 mG 
H OG  H G   H L
 L 
 (G ' ) 
HG  ScG
( L' ) 
The heights of gas and liquid transfer units have been correlated 
 L' 
H L     Sc L
 L 
Where, HG and HL are in meters, G’ and L’ are in kg/m2-sec, μL is in kg/m-sec and the gas
and liquid Schmidt numbers are

ScG  
G   L 
  G DG  and Sc L    L DL 
DG and DL are the gas and liquid diffusivities respectively of the solute absorbed
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Problem (Homework)

Determine the height of a packed tower that is used to


reduce the conc. of H2S in air from 0.1 kg/m3 to 0.005
kg/m3 given the following data:
Incoming liquid is water free of H2S
Operating temperature – 250C
Operating pressure 101.325 kPa
Henry’s law constant = 5.522
HG = 0.444m; HL = 0.325m
Liquid flow rate = 20 kg/s
Gas flow rate = 5 kg/s

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Solution

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Adsorption
Adsorption is a surface phenomenon by which gas or liquid molecules
are captured by and adhere to the surface of a solid adsorbent
Physical Adsorption
 The gaseous material condenses upon the surface of the solid,
accompanied by an evolution of heat
 The adsorbed material can be removed or desorbed by reducing
the pressure or by increasing the temperature. Thus, the process is
reversible
Chemisorption
 Chemical interaction between the solid and the adsorbed material
 It is irreversible process
 Heat of adsorption being much higher than that for physical
adsorption
 The molecules are held to the solid surface by chemical bonds and
the original material undergoes a chemical change

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Adsorption
Adsorption techniques are widely used in the field of:
 Odor control for removing small quantities of pollutants
present in a large volume of air
 For collecting valuable organic substances that cannot be
picked up by scrubbing methods
Adsorption rate depends on several factors:
 Concentration of the material around the adsorbent
 Surface area of the adsorbent
 Pore volume of the adsorbent
 Temperature, molecular polarity and the chemical nature of
the adsorbent surface

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Desirable characteristics of
adsorbents
Desirable Qualities of Adsorbents: High adsorptive ability ,
Large surface per unit mass, Must not offer high
pressure drop, Adequate strength and hardness and
Free flowing.

Manchisi, James & Matinde, Elias & Rowson, Neil & Simmons, Mark & Simate, Geoffrey S. & Ndlovu, Sehliselo & Mwewa, Brian. (2020). Ironmaking and Steelmaking Slags as Sustainable
Adsorbents for Industrial Effluents and Wastewater Treatment: A Critical Review of Properties, Performance, Challenges and Opportunities. Sustainability. 12. 2118. 10.3390/su12052118.
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Adsorption
Mechanism - Adsorption
 The diffusion of the pollutant from the bulk gas phase to the
external surface of solid
 The diffusion of the gas molecules into the pores of the solids
 And finally is the actual adsorption on the active sites in the pores
Removal of pollutants by adsorption may be carried out in a batchwise
or continuous manner of operation
Adsorption Isotherm
 Relation between amount of pollutant adsorbed and the
equilibrium pressure at constant temperature
*
aC g
W *
1  bC g

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Adsorption Isotherm

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Adsorption Mechanism
Clean
Effluent
 The diffusion of the pollutant from
the bulk gas phase to the external
surface of solid
 The diffusion of the gas
molecules into the pores of the
solids
 And finally is the actual
adsorption on the active sites in
the pores
Dirty
Effluent

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Adsorption in Fixed Bed

LUB
Length of
Unused Bed

𝒕 = 𝒕𝟏 𝒕 = 𝒕𝟐 𝒕 = 𝒕𝟑

MTZ
Mass Transfer Zone
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Fixed Bed Adsorption Process

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Ideal and Actual Outlet Concentration Curves


Outlet Concentration

Time (h)

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Mathematical Analysis of
Fixed Bed Adsorption

1. The velocity with which the


adsorption wave moves
through the bed, u is given
by

0.5
cout/
2. Length of Mass Transfer 𝑐
Zone

3. Length of Unused Bed 𝑡 𝑡 𝑡 𝑡∗


(LUB)

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Adsorption

Breakthrough Time (tB)

a,b = Langmuir coefficients


Cg* = Equilibrium concentration of pollutant g/m3
Qg = Volumetric flow rate of gas
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9-43

Determine the breakthrough time for toluene on an


adsorption bed of activated carbon that is 0.75 m thick and
5 m2 in cross section. The operating parameters for the bed
are as follows:
Gas flow rate = 1.185 kg/s
Gas temperature = 250C
Bed density = 450 kg/m3
Inlet pollutant concentration = 0.00350 kg/m3
Langmuir parameters: a = 465, b = 3000
Width of adsorption zone = 0.045m

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Environmental Pollution Control


ETZC362/PEZC411
Prof. Krishna C. Etika
Associate Professor
BITS Pilani Department of Chemical Engineering
Pilani Campus B.I.T.S-Pilani, Pilani Campus

ETZC362/PEZC411 Environmental Pollution Control

Water Pollution

Sources and Classification of water


pollutants

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Water in India!
• NITI Aayog reported that 600 million people in India encounter
extreme to high water stress.

• With a decadal growth of 17 %, the expanding urban population


largely contributes to water demand and water pollution from
domestic and industrial wastewater discharges.

• Extensive migration of rural population to cities has led to an


upsurge in utility services resulting in overexploitation of ground-
waters.

• Besides expanding population, industrialization accounts for about


a 4 % rise in water demand annually resulting in a substantial
increase in industrial wastewaters volume.

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Water in India
• It is estimated that the total water demand for domestic, industrial and
agricultural sectors will rise to 103 billion cubic metres (BCM) in 2025
and 1447 BCM by 2050.

• Disproportionate distribution of natural water resources due to diverse


geographies, climate change and irregular monsoons, trade and
commerce further challenge water management in India.

• With 21 major cities nearing water depletion and various cities being
subjected to water supply cuts, India now ranks thirteen in the list of
water-stressed countries.

• India is home to 1.4 billion people and the wastewaters generated varies
from 15 to 135 L/per person/day which imposes critical challenges in
developing low-cost wastewater treatment technologies that meet the
current discharge standards.
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Some Calculations!
How much wastewater (approximate) will be generated today in India?

Today’s Population: 1,432,412,510 (As per Worldometer!)

Average wastewater generated : (15+135)/2=75L/person/day

Total Wastewater generated: 1.075 x 1011 L/day


: 1.075 x 108 m3/day
: 3.92 x 1010 m3/year

Annual Precipitation : 4 x 1012 m3/year

Water required 1.03 x 1011m3/year in 2025

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Outline
– Water resources
– Origin of wastewater
– Classification of water pollutants
• Oxygen demanding waste
• Disease causing agents
• Synthetic organic compounds
• Plant nutrients
• Inorganic chemicals and minerals
• Sediments
• Radioactive substances
• Thermal discharges
• Oil

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Water Resources

Water is vital natural resource which is essential for a


multiplicity of purposes.
Water used
 Drinking
 Domestic uses
 Industrial cooling
 Power generation
 Agriculture (irrigation)
 Transportation
 Waste disposal

 Main source of water in India is rain

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Hydrologic Cycle

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Hydrologic Cycle
• Natural cycle : More than 97% of water in biosphere is in oceans, the
remaining 3% is found in continents and atmosphere
• More than 70% of this is in glaciers and icecaps
• Water on which human depend such as lakes, streams and ground water
accounts for less than 1% of total supply
• The hydrologic cycle of the biosphere depends on the reciprocity of
evaporation and precipitation.
• Liquid water on earth goes to the atmosphere as vapor by evaporation
and transpiration of the plants. The vapor is returned to Earth as rain or
snow over the oceans.
• Oceans lose more water by evaporation than they gain by precipitation.
• The difference is made up by runoff and seepage from the continents,
over which there is more precipitation than evaporation.
• Continents lose more than 50% of the precipitation through evaporation
and remainder is stored in lakes, rivers or ground water which is later
discharged into oceans.
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Water for Human Use

• Each year about 4,23,000 km3 water is evaporated, and


the same quantity is precipitated.
• Amount of water temporarily stored & later discharged
into oceans is 37000 km3
• This is the only water is available for human use!
• Minor modification by diverting or regulating the runoff
and storage.

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Season–wise distribution of
rainfall in India
Duration Approximate % of the annual rainfall
January-February 2.6
March–May 10.4 Scarcity of water
June–September 73.7 …….. Flood
October–December 13.3
100%

Estimated Rainfall
 17.5% water evaporates
 20% water runs off into surface water bodies (river + pond + … )
 53.5% water percolates into the soil
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Rainwater Fate

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Indian Context

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S.K. Jain, CURRENT SCIENCE, VOL. 102, NO. 7, 10 APRIL 2012, 964-67 BITS Pilani, Pilani Campus

ETZC362/PEZC411 Environmental Pollution Control

Sources of Water
Alternative water source for human
 Desalinated sea water (for drinking purpose)
 Reclaimed waste water (for irrigation, sanitary and fire
fighting)
Utilization of water:
 1. Irrigation:
 Water requirement for the irrigation is the highest.
 Water requirement for irrigation varies with the climate and the type of crop being
raised.
 Surface water used for irrigation may be diverted through canals.
 Dams can be used to make water available during the shortage time period.

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Domestic water supply

 Domestic water requirement also varied from the season


to season.
 The water requirement in the cities is much higher than
villages.
 Water use in the cities is directly proportional to the
standard of living.
 The per-capita water consumption is the criteria which
define the standard of living in a particular area.
 It is very difficult to find it correctly as public do not fully
rely on the municipal water supply.

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Power Generation

 Water is converted into steam in the thermal power


plants and the turbines are rotated to produce electricity.
 The principal water demand is in the cooling
requirements in the boilers.
 The heated water some times discharged in the open
and it leads to the water loss through the evaporation.
 On a rough estimate in a 500MW power plant about 40
million litres of water would evaporate per day.
 As the electricity demand is increasing the water
wastage would increase.

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Industrial water use

 Industry is much dependent on adequate water supplies.


 Water requirement also varied from industry to industry.
 Major water consuming industries are steel, paper and
pulp, textiles, chemicals and petroleum refining.
 With the increase of the industrialization the water
demand is also going to increase.

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Origin of Wastewater
Waste water (by the origin)
• Point sources: collected by a network of pipes or channels
and conveyed to a single point of discharge into the
receiving water
• Domestic sewage
• Industrial wastes
• Non-point sources: characterized by multiple discharge
points
• Agricultural runoff
• Urban runoff
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Water Pollution
Domestic and industrial wastes pollute the aquatic
systems.
 75 to 80% of India’s population is exposed to unsafe
drinking water.
 Fertilizers are getting discharged into water bodies and
causing eutrophication.
 Pesticides are entering the food chain.
 Fish are being killed in millions along sea coasts.

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Waste water characteristics


• Varies widely from industry to
industry
• Because of the large number
of pollutant substances,
wastewater characteristics
are not usually considered on
a substance by substance
basis.
• Rather, substances of similar
pollution effects are grouped
together into classes of
pollutants or characteristics
• The specific characteristics
will affect the treatment Perry’Chemical Engineers’ Handbook, 8th Edition
techniques
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Classification of water
pollutants
1. Oxygen demanding wastes
2. Disease–causing agents
3. Synthetic organic compounds
4. Plant nutrients
5. Inorganic chemicals and minerals
6. Sediments
7. Radioactive substances
8. Thermal discharges
9. Oil

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Classification and sources

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Types of Water Pollutants

Disease causing Agents


 Water carries pathogenic micro-organisms, which come
from tanning and meat packaging industries. Some
bacteria are water-borne. These disease causing agents
cause cholera, typhoid, dysentery.
 Viruses are also found in water, which are responsible
for polio, infectious hepatitis and fever.
 Water also plays an indirect role in the transmission of
diseases like malaria, yellow fever.
 Presence of pathogens make the water unfit for drinking,
at high concentration, water may also be unsafe for
swimming and fishing

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Types of Water Pollutants

Synthetic Organic compounds (Pesticides, detergents)


 Pesticides and detergents are not biodegradable and may
persist for long periods reaching objectionable levels in water
or in aquatic life. Wide variety of these compounds are not
being detected.
Pesticides
 Insecticides
 Herbicides
 Fungicides
Pesticides result primarily from surface run off from agricultural
lands, water discharge by pesticide manufacturers and by
other means. Because of their world wide usage, nearly all
the rivers and oceans of the world contain pesticide residues.
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Limiting standards for some common pesticides in drinking water


are given as:
Pesticides Max Permissible limit (mg/l)

Aldrin 0.017
Chlordane 0.003
DDT 0.042
Dieldrin 0.017
Endrin 0.001
Heptachlor 0.018
Heptachlor Epoxide 0.018
Lindane 0.056
Toxaphene 0.005
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Detergents

 The basic active ingredient in detergents is the surfactant or


surface active agent.
 It lowers the surface tension and allows dirt particles to
become linked to water. The dirt is subsequently lifted or
floated from the soiled garment during the washing process.
 Surfactant concentration as low as 1 ppm produce foam in
rivers and in sewage treatment plants. Although these
concentration are non-toxic to humans, the presence of
surfactants gives on off-taste to drinking water.
 The presence of surfactants reduces the rate of oxygen
absorption in water.
 The acceptable concentration for surfactants in water supplies
has been set at 0.5 ppm.

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Plant Nutrients

 Nitrogen and Phosphorus are essential elements which are


required by plants and animals for maintaining their growth
and metabolism.
 Small amount of nitrates and phosphates occur in all aquatic
systems and these are sufficient to maintain a balanced
biological growth.
 Huge amount of nitrates and phosphates may enter the water
bodies directly from the manufacture and use of fertilizers,
and from the processing of biological materials such as food
and textiles, or via domestic sewage treatment plants.
 Thus water unusually large concentration of nutrients are
present in water bodies, an excess growth of algae appears.

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 This produces an unsightly green slime layer over the surface


of the water body and subsequently leads to eutrophication.
 The slime layer reduces light penetration and restricts
atmospheric reoxygenation of the water.
 The dense algal growth eventually dies and the subsequent
biodegradation produces an oxygen deficit which can result in
foul-smelling anaerobic conditions.
Inorganic chemicals and Minerals
Inorganic acids
Inorganic salts
Metal and metal compounds

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Inorganic Acids

Source:
a)Mine drainage (mining of sulphur bearing ores
containing lead, zinc, copper and iron sulphide
(pyrite)
b)Acidic rainfall
Effects:
a)Acids cause corrosion of metals and concrete
b)Acids are fatal to fish

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Inorganic Salts

Source: Industrial effluents, salt from mines or from oil


wells, and ocean salts.
Effects:
• Salts causes hardness of water
• Hard water can cause scale formation in pipes, boiler
tubes and other industrial equipments
• Fatal to fish.

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Metals
Cadmium
Source: waste streams from pigment works, textiles, electroplating,
chemical plants etc.
Permissible Level: 0.01 mg/l (drinking water)
Effects: It is not easily detectable in filtered water, particularly if the pH
is neutral or alkaline.
Itai-Itai disease in Japan was probably due to cadmium
Chromium
– Source: Waste water of plating operations, paint and dye
operation, wastewater from textile, ceramic and glass industry.
– Permissible level: 0.05 mg/l (Drinking water)
– Effects: Many plant species are adversely affected by chromium

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Metals
Lead
Source: Effluents from battery manufacture, printing, painting.
Permissible Level: 0.05 mg/L (Drinking water)
Effects: Is a cumulative poison and responsible for cancer.
Mercury
Source: Effluents of Pesticides, Fertilizer Paint and paper,
Chlorine industry
Permissible Limit : 0.002 mg/l (Drinking water)
Effects: Most toxic aquatic pollutant effects on photosynthesis
rate.

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Sediments
Sediments include soil, sand and mineral particles
Source:
a) By storms and flood waters
b) Deposits of sewage sludge, pulverized coal ash,
industrial solids.
Effects:
a) Pumping equipments, power turbines are affected.
b) Reduces the amount of sunlight, food etc. for water
plants, fish and other aquatic bodies.

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Radioactive substances
Source: Wastes of uranium refining, thorium mining,
wastes from nuclear power plants, and from industrial
use of radioactive materials.
Effects: Radioactive substances can enter humans with
food and water, and get accumulated in blood, and
thyroid gland, liver, bone and muscular tissues.

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Thermal Discharge

Source:
 Power plant industry uses large qualities of water for
cooling purposes and directly discharge to water bodies.
 Consequently, the water temperature is increased, and
hot water layer at the top and cold water layer at the
bottom are formed.
 The hot layer denies the oxygen transfer from
atmosphere to cold water.
 Thus, DO levels falls rapidly. And at high temperature the
metabolic activity of micro-organisms is increased.
 So, the increase of temperature results to decrease of
DO level and to increase of oxygen consumption.

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Thermal Discharge
Effects:
a) Fish death
b) An increase in temperature also increases the toxicity of
some chemical pollutants.

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Oils
o Oil spills make up about 12% of the oil that enters the
ocean. The rest come from shipping travel, drains and
dumping.
o An oil spill from a tanker is a severe problem because
there is such a huge quantity of oil being spilt into one
place.
o Oil spills cause a very localised problem but can be
catastrophic to local marine wildlife such as fish, birds
and sea otters.
o Oil cannot dissolve in water and forms a thick sludge
in the water. This suffocates fish, gets caught in the
feathers of marine birds stopping them from flying
and blocks light from photosynthetic aquatic plants.
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ETZC362/PEZC411
Prof. Krishna C. Etika
Associate Professor
BITS Pilani Department of Chemical Engineering
Pilani Campus B.I.T.S-Pilani, Pilani Campus

ETZC362/PEZC411 Environmental Pollution Control

Water Pollution

Sources and Classification of water


pollutants

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Oxygen Demanding Wastes


(DO & BOD)
 Dissolved oxygen (DO) is essential for sustaining the plant and
animal life in any aquatic system.
 For example, warm water fish requires a minimum DO level of at
least 5 mg/l.
 If the DO level drops below the level necessary to sustain normal
life, then the aquatic system is classified as polluted.
Process by which the DO content is affected
(a)Reaeration: Process by which oxygen transfer takes place from the
atmosphere to water.
(b)Photosynthesis
(c)Respiration
(d)Oxidation of wastes
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Oxygen Demanding Wastes


(b) Photosynthesis: Requires solar radiation
During Photosynthesis
 Green plants (algae) utilize CO2 and produce O2
 Organic materials are synthesized and produce O2
Since, photosynthesis occurs only in presence of sunlight, so the DO
level in the water increases during the day.
(c) Respiration:
 The bacterial and algal respiration is responsible for the production
of CO2 and subsequent depletion of DO.
(d) Oxidation of wastes:
 The organic substances are called oxygen demanding wastes.
When these substances enter a waterway, DO is consumed in their
breakdown by micro-organisms.

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Dissolved Oxygen
When the DO level falls below the saturation value, oxygen
diffuses from the atmosphere at a rate which is proportional to
the deficit.
Interface
Air
water

Cs

CL

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Diurnal DO Variation

Saturation
DO

12 6 12 6 12
Midnight A.M. Noon PM Midnight

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Diurnal DO Variation

Saturation

DO

12 6 12 6 12
Midnight A.M. Noon PM Midnight

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How DO is Measured
Dissolved Oxygen Meter:
Principle: Electrochemical sensors are used to
measure the concentration of oxygen in the
water.
Operation: The sensor consists of a cathode
and an anode placed in an electrolyte
solution. Oxygen diffuses through a gas-
permeable membrane to the cathode, where
it undergoes a reduction reaction, generating
a current proportional to the oxygen
concentration.
Advantages: Provides accurate and real-time
measurements. Portable and easy to use in
the field.
Applications: Suitable for both field and
laboratory measurements. Commonly used in
environmental monitoring and research.
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Oxygen Transfer Rate

Oxygen (air) is sparingly (not highly) soluble in water. So,


the main resistance to mass transfer is from the liquid
side or liquid film controlling (kl = KL)

 mass of O 2 transfer 
N  Mass Flux   ,
 unit area of surface  time 
N = KL (CS – CL)
KL = Liquid Phase Mass Transfer Coefficient
CS = Conc. of DO at saturation (interface)
CL = Actual conc. of DO in the water

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Oxygen Transfer Rate

The rate of oxygen transfer (mass/time) into unit volume of


water (v) is given by:

dC L NA A
  K L C S  C L   k 2 C S  C L 
dt V V
Where,
KL A
k2  = Reaeration rate constant /reoxygenation rate constant
V
dC L
 Oxygen transfer rate
dt
D= (CS-CL)= Oxygen deficit
10

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Problem 1

A water sample is collected from a river for oxygen demand


analysis. The initial dissolved oxygen in the sample is 8
mg/L, and after incubation for 5 days, the dissolved
oxygen concentration drops to 2 mg/L. Calculate the
oxygen deficit in the water sample.

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Typical values of KL
Types of Water KL (m/day)

Stagnant water 0.10-0.15


Water flowing at 0.6 m/min 0.25
Sluggish polluted river 0.5
Sluggish clean water about 5 cm 1.0
deep
Water flowing at 10m/min 2.0
Open sea water 3.0
Water flowing at 15m/min 7.0

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Problem 2

• A water sample is collected from a clear river flowing at


10m/min for oxygen demand analysis. The initial
dissolved oxygen in the sample is 8 mg/L, and after
incubation for 5 days, the dissolved oxygen
concentration drops to 2 mg/L. Calculate the flux of O2
that would have diffused from atmosphere in a
waterbody comprising of 1000000 L of the river water.

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Biochemical Oxygen Demand


Pollution results when the oxygen demand exceeds the
available oxygen.
Biochemical Oxygen Demand (BOD)
 Is a measure of the O2 utilized by microorganisms during
the oxidation of organic materials.
 On an average, the demand for oxygen is directly
proportional to the amount of organic waste which has to
broken down.
 Hence, BOD is a direct measure of oxygen requirements
and an indirect measure of biodegradable organic
matter.

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Biochemical Oxygen Demand


When a water sample containing degradable organic matter is placed in a closed
container in the presence of bacteria, the O2 consumption follows the pattern shown
below

L = The amount of BOD remaining in time t or the conc. of the remaining


oxidizable material (mg/l)
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Biochemical Oxygen Demand


If a given amount of organic matter is introduced into a water sample
and its decomposition is monitored, one would observe that the rate
of oxidation of organic matter (rate of decline of BOD) can be
approximated as a first-order chemical reaction whose kinetics may
be expressed as:
dL
  k1 L
dt
L = The amount of BOD remaining in time t or the conc. of the
remaining oxidizable material (mg/l)
k1 = The reaction rate constant or deoxygenation constant, day-1
Let at t = 0, L = Lu = Ultimate BOD (the original concentration of the organic
material before any biological action has occurred), we can integrate to get
L '
k1
 exp(  k 1t )  10  k1t Where k 1 
Lu 2 . 303
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Biochemical Oxygen Demand



 L  L u 10  k1 t 
If y represents the amount of BOD utilized at any time t, then
Lu = L + y

or 
y  Lu  L  Lu 1  10  k1 t 
A standard way to measure BOD is to determine the amount of
O2 required by the bacteria during the first five days of
decomposition at 200C. The result is known as the 5-day BOD
at 200C, commonly abbreviated as BOD5 that is equals

y5  Lu  L5  Lu 1  10 5 k1 
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Biochemical Oxygen Demand

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Question?

If we know Lu and k1ʹ, we can predict the BOD


at any time t.

How can we get Lu and k1ʹ ???

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Thomas method
Determination of k’1 and Lu is done using Thomas method

The method is based on the similarity of two functions

1  10 
3
 k1t   2 .3   
And 2 . 3 k 1 t  1    k1 t 
  6  

1  10  2.3 k  t 1  12 2.3 k  t   16 2.3k t 


 k1 t
1 1 1
2

1
24
2.3 k1t 3  ....
 
3
  2.3    1
2.3 k1t 1  
1
 k1 t   2.3 k1t 1  2.3 k1t   2.3 k1 t  
2 1
2.3k1t 3  ....
  6    2 6 21.6 

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Thomas method
As can be seen, the first three terms within the brackets in the
two series are identical, and the difference between the fourth
term is small. Hence, the equation (6) can be written as:

3
  2.3  
y  Lu 2.3K1t  1    k1t 
  6  

Taking the inverse and the cube root, and rearranging, we get

1
t 3 1  K   2 3 
 2.3 K 1 Lu 

  3  1
t
 3.43 Lu  3 
1
 y
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Thomas method
A plot of (t/y)1/3 vs time, t, will give a straight line whose slope,
b and intercept, a can be used to calculate K’1 and Lu.
1   K  2 3 
a  2.3 K1 Lu 

3 b 1
1 
 3.43 Lu  3 
Further simplification will yield,

b 1
k1  2.61 Lu 
a 2.3k1 a 3
If we know k1ʹ and Lu, it is possible to predict the BOD utilization
with time.

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y  Lu  L  Lu 1  10  k1 t  22
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Problem 3
BOD results for a sample at 200C. Determine k1’ and Lu.
t (days) 0 1 2 3 4 5
Y (BOD in mg/l) 0 65 109 138 158 172

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Solution
BOD results for a sample at 200C. Determine k1’ and Lu.
t (days) 0 1 2 3 4 5
Y (BOD in mg/l) 0 65 109 138 158 172

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Typical values of K’1 and Lu

Type of Waste water K11 (day-1) Lu(mg/l)


Weak wastewater 0.152 150
Strong wastewater 0.168 250
Primary sewage effluent 0.152 75-150
Secondary sewage effluent 0.052-0.100 15-75

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Deoxygenation constant (k1`)

The deoxygenation constant is f(Temperature) like any


other reaction rate constant.

Van’t Hoff-Arrhenius equation is applicable.

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Deoxygenation constant (k1`)

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Problem 4

Show that the ratio of 2.25 –day 35oC BOD to 5-day 20oC
BOD is almost 1.

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Complete BOD Curve

Why two stages??


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Complete BOD Curve

 During the carbonaceous stage, ammonia is produced


by the breakdown of organic nitrogen materials, but this
process is so slow that nitrifiers do not dominate till
end of this stage.

Nitrosomonas
2NH4+ + 3O2 2NO2- + 2H2O + 4H+
Nitrobacter
2NO2- + O2 2NO3-
 Ammonia exerts a very high O2 demand, requiring more
than 3 times its own weight of oxygen for complete
oxidation.

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Complete BOD curve – New

Allylthio Urea - Inhibitor


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Oxygen Sag Curve


• Waste discharge to water results in depletion of DO
• As DO drops below saturation level, reaeration takes place.
• The simultaneous action of deoxygenation and reaeration results in
a typical variation of DO concentration of aquatic system known as
oxygen sag curve

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Environmental Pollution Control


ETZC362/PEZC411
Prof. Krishna C. Etika
Associate Professor
BITS Pilani Department of Chemical Engineering
Pilani Campus B.I.T.S-Pilani, Pilani Campus

ETZC362/PEZC411 Environmental Pollution Control

Water Pollution

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Complete BOD Curve

Why two stages??


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Complete BOD Curve

 During the carbonaceous stage, ammonia is produced


by the breakdown of organic nitrogen materials, but this
process is so slow that nitrifiers do not dominate till
end of this stage.

Nitrosomonas
2NH4+ + 3O2 2NO2- + 2H2O + 4H+
Nitrobacter
2NO2- + O2 2NO3-
 Ammonia exerts a very high O2 demand, requiring more
than 3 times its own weight of oxygen for complete
oxidation.

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Complete BOD curve – New

Allylthio Urea - Inhibitor


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Oxygen Sag Curve


• Waste discharge to water results in depletion of DO
• As DO drops below saturation level, reaeration takes place.
• The simultaneous action of deoxygenation and reaeration results in
a typical variation of DO concentration of aquatic system known as
oxygen sag curve

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Oxygen Sag Curve:Critical k = deoxygenation rate constant, d -1

Deficit and Critical Time


1
k = re-aeration rate constant 2

Net rate of change of oxygen deficiency, dD/dt


dD/dt = k1L - k2D where L = Lue-k1t
dD/dt = k1Lue-k1t - k2D
Do = deficit at t = 0.

k1 Lu
D (e  k1t  e k 2t )  Do e  k2t
k 2  k1
At maximum deficit, i.e., D=Dc
k1
dD
 k1 Lu e  k1t  k 2 D  0 Dc  Lu e  k1t
dt k2
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Oxygen Sag Curve:Critical


Deficit and Critical Time
The critical time (tc) can be obtained by differentiating the eqn
below and setting dD/dt = 0

k1 Lu
D (e  k1t  e k 2t )  Do e  k2t
k 2  k1
1. Differentiating w.r.t t
2. LHS  0 at t=tc

1 k  D o ( k 2  k 1 )  
tc  ln  2 1  
k 2  k1  k1  k1 Lu  

How to determine k1 and k2?


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Critical Deficit and Critical


Time
k1 = can be determined by BOD test in the laboratory (Thomas
method) and using the Bosko Equation:
 v
k1  k1, BOD   
 h
k1 = deoxygenation rate constant at 20oC, d-1
ν = average speed of stream flow, m/s
k1,BOD = BOD rate constant determined in laboratory at 20oC, d-1
h =average depth of stream,
η = bed-activity coefficient (0.1 for stagnant or deep water, 0.6 for rapidly flowing water)

k2 = f(stream characteristics). Estimated using the eqn


3.9v 0.5
k 2  1.5
h 9
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Mixing Concentraton

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Mixing Concentration
Concentrations of DO and BOD after mixing are the
respective masses per unit time divided by the total flow
rate (sum of wastewater and river flow)
Qw Lw  Qr Lr
Lo 
Qw  Qr

 Q DO w  Q r DO r 
D o  DO s   w 
 Qw  Qr 

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Problem 5

A town discharges 17360 m3/day of sewage into a nearby


stream. The stream has a minimum flow of 0.4 m3/s,
depth of 2.5 m and velocity of 5 kmph. Other information
is given below:
Temp (oC) DO(mg/l) BOD5(mg/l)
Stream 20 8.5 10
Sewage 25 1.0 200

The deoxygenation constant (k1) evaluated at 20oC = 0.35


d-1 . Determine the critical deficit and its location.

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Solution

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Solution

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Solution
3.9v 0.5
k2 
h1.5

 Q DO w  Q r DO r 
D o  DO s   w 
 Qw  Qr 

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Water quality monitoring

• Helps in identifying the present and future problems of


water pollution
• Identifying the present resources of water as per various
usages
• helps in developing plans and setting priorities for water
quality management programme so as to meet future
water requirements
• helps in evaluating the effectiveness of present
management actions being taken and devising future
course of actions

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Waste Water Sampling

• The sampling method used should be one that gives a


representative picture of the quality of the waste stream;
otherwise, the time and effort involved in the analysis will
be completely wasted.
• Sampling
– The grab sample
– The composite sample

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The grab sample

• It shows only the prevailing conditions at the time of


sampling and cannot represent average conditions.
• Hence it should not be used as a basis for treatment.
• However, grab samples are useful in determining the
effects of extreme conditions of waste during the time
composite samples are being collected or when the
waste water flow is intermittent.

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Composite Sample
• It provide more meaningful data when the composition of
the waste varies with either time or flow.

• A composite sample can be obtained by collecting individual


samples at frequent intervals and mixing them together.

• These samples can be collected manually or with automatic


samplers on the basis of flow and time.

• When waste water flow and composition are relatively


uniform, grab samples of a fixed volume can be manually
taken at given time intervals and composite sample obtained.

• If flow rate varies the volume of the grab sample collected is


proportional to the flow.

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Sampling

• For physical examination, water can be collected in fully


cleaned ordinary buckets or plastic cans.
• If the water is to be collected for chemicals tests, the
container, usually glass bottles of more than 2 liter
capacity, should be thoroughly washed and cleaned; and
then the water should be collected in it
• For the collection of water for bacteriological tests, the
person who collects the water must be free from any
disease.
• The containers and bottles must be cleaned with
sulphuric acid, potassium dichromate or alkaline
permanganate, and then, they should be thoroughly
rinsed with distilled water and finally sterilization
should be done
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Some Water Quality Parameters.


Physical Chemical Biological
• Color • Acids or alkali • Algae
• Conductivity • Ammonia • Bacteria
• Odor • Biochemical oxygen demand (BOD) • Pathogens
• Radioactivity • Calcium • Protozoa
• (BOD) • Chloride • Viruses
• Solar radiation intensity • Chlorophyll
• Suspended solids or • Chemical oxygen demand(COD)
sludges • Dissolved oxygen (DO)
• Temperature • Hardness
• Turbidity • Heavy metals: Chromium, Copper,
Iron, Lead, Manganese, Mercury.
• Magnesium.
• Nitrate, nitrite
• Organic compounds: Detergents,
Herbicides, Pesticides, Phenol, Oils
and greases.
• Oxidation-reduction potential
• pH
• Phosphates
• Potassium
• Sodium
• Sulfate
• Total organic carbon (TOC) 22
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BOD Determination Procedure


 BOD is the amount of oxygen (Dissolved Oxygen (DO))
required for the biological decomposition of organic matter.
 The oxygen consumed is related to the amount of
biodegradable organics.
 The most widely used measure of bio-degradable organic
content of waste water is the 5-day, 20˚C BOD value.
 The brief analytical procedure is:
– Two standard 300 ml BOD bottles are filled completely
with the waste water of which the BOD is to be
measured and the bottles are sealed.
– Oxygen content of one bottle is determined immediately.
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BOD Determination Procedure


– The other bottle is incubated at 20˚C for 5 days in total
darkness (to prevent algal growth) after which its oxygen
content is measured.
– The difference between the two DO values is the amount
of oxygen that is consumed by microorganism during the
5 days and is reported as the BOD5 value of the sample.

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BOD Determination Procedure


• Since the saturated value of DO for water at 200C is 9.1
mg/L only and that the oxygen demand for wastewater may
be of the order of several hundred mg/L,
• This can make the test indeterminate!
• wastewater are generally diluted so that the final DO
in BOD test is always ≥ 2 mg/L.
• Precaution is also taken so as to obtain at least 2 mg/L
change in DO between initial and final values
• BOD5 (in mg/l) = [DOi – DOf] x D
• Where D = dilution factor = (total diluted volume/sample
volume)
• NOTE: Here it is assumed that the diluted wastewater
had no oxygen demand of itself and that the dilution
wastewater used was pure.
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BOD
 Most of the times, microorganisms are added in the
dilution water (seeded water) so as to have enough
microorganisms for carrying out biodegradation of
organic waste.

 In this case, the oxygen demand of seeded water is


subtracted from the demand of mixed sample of waste
and dilution water.
 BOD5 (in mg/l) = [(DOi,s – DOf,s)-(DOi,B – DOf,B)f] x D
f= (V2-V1)/V2 , D= V2/V1
 DOi,B and DOf,B are initial and final DO concentrations of
the seeded diluted water (blank).
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BOD Determination : Practical


Aspectes
In order to calculate the BOD, the laboratory collects the samples
of waste water and then dilutes it in a BOD incubation bottle.
The lab must measure the following data :
• D1 = oxygen diluted level in the diluted sample at t=0 (mg/l)
• D2 = oxygen diluted level in the diluted sample at t=5 days (mg/l)
• B1 = oxygen diluted level in the dilution water at t=0 (mg/l)
• B2 = oxygen diluted level in the dilution water at t=5 days (mg/l)
• V1 = volume of wastewater sampled for dilution (ml)
• V2 = volume of diluted sample (ml)

The BOD at 5 days can be calculated with the following BOD calculation formula :
BOD5 = [(D1-D2)-(B1-B2)f]/P
f = (V2-V1)/V2
P = V1/V2
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Problem 2

A factory has taken a sample of its effluents and sent it to


the lab. The lab takes 10 ml of waterwater and dilute it in
a BOD incubation bottle of 250 ml. The lab measures the
oxygen level in the diluted water and gets 10 mg/l at t=0
and 2 mg/l at t=5 days, it takes also the same measures
on the dilution water and gets 9.5 mg/l at t=0 and 8 mg/l
at t=5 days. The lab wishes to calculate the BOD5 of the
effluent.

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Solution

D1 = oxygen diluted level in the diluted sample at t=0 = 10 mg/l


D2 = oxygen diluted level in the diluted sample at t=5 days = 2 mg/l
B1 = oxygen diluted level in the dilution water at t=0 = 9.5 mg/l
B2 = oxygen diluted level in the dilution water at t=5 days = 8 mg/l
V1 = volume of wastewater sampled for dilution = 10 ml
V2 = volume of diluted sample = 250 ml

f = (V2-V1)/V2 = (250-10)/250 = 0.96


P = V1/V2 = 10/250 = 0.04

BOD5 = [(D1-D2)-(B1-B2)f]/P = [(10-2)-(9.5-8)*0.96]/0.04 =


164.4 mg/l

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Chemical oxygen demand


• This test is carried out on the sewage to determine the extent
of readily oxidizable organic matter, which is of two types:
• Organic matter which can be biologically oxidized is
called biologically active
• Organic matter which cannot be oxidized biologically is
called biologically inactive.
• COD gives the oxygen required for the complete oxidation of
both biodegradable and non-biodegradable matter.
• COD is a measure of the oxygen equivalent of the organic
matter content of a sample that is susceptible to oxidation by
a strong chemical oxidant.
• It is an indirect method to measure the amount of organic
compounds in water.
• It is expressed in milligrams per liter (mg/L), which indicates
the mass of oxygen consumed per liter of solution.
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Chemical oxygen demand


• In the COD test, the oxidizing bacteria of the BOD test are
replaced by a strong oxidizing agent under acidic
conditions.
• A sample is mixed with an excess of potassium
dichromate and sulphuric acid and the mixture is heated
under total reflux conditions for a period of 2 hours.
• During digestion, the chemically oxidisable organic
material reduces a stoichiometricaly equivalent
amount of dichromate.
• The remaining dichromate is titrated with standard
ferrous ammonium sulphate solution.
• Procedure is applicable to COD values between 40-400 mg/l
Organic C+Cr2O7-  CO2+H2O+Cr2O4-
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Chemical oxygen demand


• The amount of potassium dichromate reduced gives a
measure of the amount of oxidizable organic material.
• Dichromate has advantage over other oxidants in oxidizing
power and applicability to a wide variety of samples.
• The COD test does not distinguish between organic
materials that are biodegradable and those that are not.
• COD always oxidize things that the BOD cannot or will not
measure
• Hence gives a measure of the total oxidizable organic
material in the sample.

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Chemical oxygen demand


• Due to this the COD test results are higher than those of BOD
tests carried out on the same sample.

• If the inorganic substances such as chlorides and nitrites are


present in the waste water, they interfere with the COD test
since they are also oxidized by dichromate and create an
inorganic COD that leads to an error in the measurement.

• The COD test is much more useful then the BOD test for
estimating the oxygen requirements of certain industrial waste
waters.

• The general relationship between BOD and COD for sewage


and most human wastes is:

• ~1 unit of BOD≈0.64–0.68 units of COD.


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Total Organic Carbon (TOC)

• Total organic carbon test is based on the oxidation of the


carbon of the organic matter to carbon dioxide, which is
measured by a non-dispersive infrared analyzer.
• Alternatively, the CO2 can be reduced to methane, which
is then measured by a flame ionisation.
• In this test, a few micro-litres (5 – 10 micro litre) of the
aqueous sample are injected into a combustion tube
containing a catalyst and heated to 900˚C in a constant
flow of air.
• Water is vaporised and the carbonaceous matter is
oxidized to CO2 and steam.
• Outside the combustion tube, the steam is condensed
and removed.
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TOC

• CO2 is swept into a non-dispersive infrared analyzer which


measures the amount of CO2.
• The concentration of CO2 is directly proportional to the
concentration of total carbon present in the original sample
and it includes both organic and inorganic carbon.
• Inorganic carbon can be measured separately using an
acid catalyst at 150˚C which is below the temperature at
which organic matter is oxidized.
• Organic carbon content can then be obtained by
subtracting the inorganic carbon from the total result.

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Determination of inorganic
substances
Hardness
• Hardness of water is due to the presence of carbonates and
sulphates of calcium and magnesium ions in the water.
• Sometimes hardness in the water can also be caused by the
presence of chlorides and nitrates of calcium and
magnesium.
• Presence of hardness in water prevents the lathering of the
soap during cleaning of clothes, etc.
• Hardness is usually expressed in mg of calcium carbonate
per litre of water.

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Hardness
• Hardness is generally determined by Versenate Method.
• The water is titrated against EDTA salt solution using Eriochrome
Black T as indicator solution. While titrating, color changes from
wine red to blue. In general, under a normal range of pH values,
water with hardness up to 75 mg/L are considered as soft and
those with 200 mg/L and above are considered as hard. In
between, the water is considered as moderately hard.
• However, for drinking purposes, water with hardness
below 75 mg/L is generally tasteless and hence, the
prescribed hardness limit for drinking ranges between 75
to 150 mg/L.

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Environmental Pollution Control


ETZC362/PEZC411
Prof. Krishna C. Etika
Associate Professor
BITS Pilani Department of Chemical Engineering
Pilani Campus B.I.T.S-Pilani, Pilani Campus

ETZC362/PEZC411 Environmental Pollution Control

Water Pollution

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Determination of inorganic
substances
1. Nitrogen:
– The important chemical species containing nitrogen in
wastewater systems are ammonia, organic nitrogen,
nitrite and nitrate.
– Ammonia exists in aqueous solution as one of the
intermediate compounds formed due to micro-biological
activity.
– Nitrogen which is tied up in high energy compounds such
as amino acids and amines is known as organic nitrogen
– Usually organic nitrogen is a potential source of
ammonia because deamination reactions that occur
during the metabolism of organic compounds release
ammonium ions.

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Nitrogen

– These two forms of nitrogen are often combined in


one measure known as Kjeldahl nitrogen.
– The Kjeldahl nitrogen is determined by digesting the
sample in sulphuric acid when the organic nitrogen
is converted to ammonia.
– The total ammonia content is measured after
neutralizing the excess sulphuric acid.

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Phosphorous

• Phosphorous exist in waste water as orthophosphate,


polyphosphate and organic phosphate.
• Orthophosphates are assimilated by bacteria during their
growth process.
• However, polyphosphate must undergo enzymatic
hydrolysis to the ortho form before they can be
assimilated.
• The organic phosphate is present in molecules such as
RNA, DNA and nucletides.
• This is also an important constituent of industrial wastes.

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Phosphorous

• Phosphorous is estimated by treating the sample with


ammonium molybdate under acidic conditions to form
molybdophosphoric acid which is reduced using vanadium
or stannous chloride or ascorbic acid when a coloured
complex is formed.
• The intensity of the colour is proportional to the phosphate
concentration in the solution.
• The vanadium method – 0.2-18 mg
• The stannous method – as low as 3 μg/l
• The ascorbic method – 20 μg/l

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Trace elements (Heavy Metals)

The standard methods used for determination of toxic


heavy metals like cadmium, chromium, lead and zinc are
the atomic absorption spectrophotometry (AAS) and
colorimetry.
The atomic absorption system consist of a light source
which emits light of a particular wavelength, an atomizer
burner unit for introducing the sample into the flame, a
prism to separate and isolate the emission lines and a
detector.

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Alkalinity

• The alkalinity in wastewaters is due to the presence of


bicarbonates, carbonates and hydroxides of metal ions such
as calcium, magnesium, sodium and potassium.
• Of these, bicarbonates are most common, since they are
formed by the action of carbon dioxide on the basic materials
such as the salts of calcium and potassium in the soil.
• Alkalinity is measured by titrating the sample with a
standard acid such as N/50 H2SO4; the results are
expressed in terms of CaCO3.
• If the pH of the original sample is higher then 8.3 the titration
is carried out using phenolphthalein indicator until it becomes
colourless.

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Dissolved solids

• The total amount of dissolved salts present in water can be


estimated by measuring the specific conductivity of water.
• The specific conductivity of water is determined by means
of a portable ionic water tester and is expressed as micro-
mho per cm at 25°C. ‘mho’ is the unit of conductivity and it
equals to 1 Ampere per volt.
• The specific conductivity of water in micro mho per cm at
25°C is multiplied by a coefficient whose value ranges from
0.5-0.8 (but generally 0.65 is used) so as to directly obtain the
dissolved salt content in mg/L.
• The actual value of this coefficient depends upon the type of
salt present in water and need other methods to evaluated it.

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Turbidity
• Turbidity is a measure of the resistance of water
to the passage of light through it.

• It is caused due to presence of suspended and


colloidal matter in the water.

• Turbidity was previously determined by Jackson


candle Turbidity units (JTU). This unit is now
replaced by more appropriate unit called
Nephelometric Turbidity unit (NTU)

• NTU is the turbidity produced by one milligram of


formazin polymer in one litre of distilled water

• WHO (World Health Organization) stipulates that


the turbidity level of drinking water should not
exceed 5 NTU and ideally should be below 1
NTU

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Colour

• Color in water is not harmful but objectionable


• Color is reported as Apparent or true color
• Apparent color is the color of the whole water sample
and
• consists of color from both dissolved and suspended
components.
• True color is measured after filtering the water sample to
remove all suspended material

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Colour

• Colour is measured by comparison with known standards.


• Coloured water made with potassium chloroplatinate when
tinted with cobalt chloride closely resembles colour of many
natural waters which are yellow brownish in appearance.
• A stock solution containing 500 mg/l of potassium
chloroplatinate with cobalt chloride added as a tinting material
is usually prepared and this is assigned colour of 500 units.
• Then a series of working standards are prepared from it by
dilution.
• The intensity of colour in water is measured against these
standards by direct visual comparison.

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Bacteriological measurements

From public health standpoint the bacteriological quality of


water is as important as the chemical quality.
The most popular method is based on determining the
content of indicator organisms in it.
The principle indicator organism used are the coliform
group of bacteria.
This group is normally non pathogenic present in polluted
waters when pathogens are or might be present.
The coliform group of bacteria has the ability to ferment
lactose or lauryl tryptose broth and produce gas.

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Bacteriological measurements

Two methods are generally used for obtaining the number


density of coliform organism in the test sample.
1. Membrane filter technique
– Here known volume of the water sample is passed
through the filter that has the very small pore size.
– The coliform bacteria are captured by the filter and
the filter is exposed to the nutrients which promote
the growth of coliform while inhibiting the growth of
others.
– After 24-48 hours the colonies of the coliform
bacteria are counted.

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The most probable number

The most probable number of coliform organism is a


statistical estimate of their density and is based on the
examination of a number of portions of different sizes of
the water sample for the presence of coliforms.

From a knowledge of the number of portions of different


sizes giving positive or negative results for coliforms the
MPN can be determined.

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Waste Water Treatment

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Outline
– Basic processes of water treatment
– Primary treatment
• Pretreatment
• Sedimentation
• Flotation
– Secondary (Biological) Treatment
• Activated sludge Process
• Trickling Filters

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Degrees of treatment

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Basic Processes of Water


Treatment
Screening, Sedimentation, floatation
Physical and filtration

Precipitation, Coagulation and


Chemical disinfections

Air stripping, Carbon adsorption,


Treatment Physical &
Oxidation and reduction, Ion
Chemical exchange, and membrane Processes

Biofiltration and Activated Sludge


Biological Process

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Primary Treatment
Primary Treatment Process

Pretreatment Sedimentation Flotation

Discrete Settling Flocculent Settling Zone Settling

Pretreatment
Is used to remove large floating and suspended solids. This
process consists of screening and then grit removal

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Pretreatment

Manually–raked bar screen

Mechanically-raked bar screen 22


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Pretreatment
Alternative of Screening: Comminutor

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Pretreatment

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Pretreatment

Bar rack (on right) in service. Comminuter (on left) out of service.
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Grit Chamber

 After screening, the wastewater enters into a grit chamber


for the removal of inorganic grit, consisting of sand, gravel
and pebbles.

 These chambers are generally designed as long chambers


and the velocities of waste flow is reduced to ~3cm/sec,
which allows settling of the grit material.

 The grit can be removed by scrappers.

 Grit chambers are provided to protect pumps from abrasion


and to reduce the formation of heavy deposits in pipes and
channels.

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Grit Chamber
Aerated Vortex

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Grit Chamber

Velocity controlled grit chamber. Left chamber in service. Right chamber out of service.
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Grit Chamber Design


Solution steps
 Calculate terminal settling velocity (stoke’s law)

 Determine the depth through which the particle has to fall


 Cross Sectional area of Flow A= Q/Veffluent
 Height of Chamber = A/W = Area/Width = particle needs
to fall this height
 Determine whether time for vertical motion (H/V) < time for
horizontal motion (L/Veffluent). If yes, it will be captured.
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Grit Chamber Design

A grit particle of diameter 0.2 mm and density of 1500


kg/m3 is to be captured in horizontal grit chamber of
length 18 m and width 1.0 m. The waste water approach
velocity carrying the grit particle is 0.3 m/s and the flow
rate is 0.15 m3/s. We would like to know whether the
particle will be settled in the grit chamber or not? The
density of waste water =1000 kg/m3 and its viscosity is
0.001 kg/m-s.

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Sedimentation

 The solids are removed by gravitational settling under


quiescent conditions.

 The sludge formed at the bottom of the tank is removed


as underflow either by vacuum suction or by raking it to a
discharge point.

 Sedimentation tanks are round or rectangular

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Sedimentation Tank

Horizontal flow
(rectangular basin)

Up flow (circular basin)

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Primary Treatment: Sedimentation

Primary Treatment Process

Pretreatment Sedimentation Flotation

Discrete Settling Flocculent Settling Zone Settling

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Types of Settling
Type Characteristics Example
TYPE 1 settling of discrete particles in dilute suspensions removal of grit and sand in
(discrete • particles have no tendency to flocculate wastewater treatment
particle • they settle as individual entities and there is no
settling) significant interaction with neighboring particles
TYPE 2 settling of flocculent particles in dilute suspensions removal of SS in primary
(flocculent as particle settle and coalesce with other sedimentation tanks of
settling) particles, the sizes of particles and their settling WWTP, settling of
velocity increases chemically coagulated
waters
TYPE 3 settling of intermediate concentration of flocculent biological floc removal in
(hindered particles secondary settling basins
settling) or • particles are so close together that interparticle of WWTP
(zone settling) forces are able to hold them in fixed positions
relative to each other and the mass of particles
settles as a zone at a constant velocity
TYPE 4 settling of particles that are of such a high occurs in the bottom of
(compression concentration that the particles touch each other deep secondary clarifiers,
settling) and settling can occur only by compression in sludge thickening
which takes place from the weight of particles facilities 34
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Sedimentation Tank

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Sedimentation Tank
 Within sedimentation,
the flow goes through a
very large area  slow
velocity
 To remove the water
from the basin quickly,
the water is directed
into a pipe or small
channel
 A series of troughs or
weirs are provided

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Clarifier Design
Clarifiers are settling tanks built with mechanical means
for continuous removal of solids being deposited by
sedimentation. A clarifier is generally used to remove
solid particulates or suspended solids from liquid for
clarification and (or) thickening

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Clarifier Design
A particle in suspension is accelerated until a limiting terminal
settling velocity (vt) is reached. The sedimentation tanks are
designed in such a way that all particles with settling velocity
greater than and equal to vt will be removed.
Critical Particle: will be one
that enters at the top of the
settling zone A, and settles
with a velocity just sufficient
to reach the sludge zone at
point B. The particle falls
through a depth H with
retention time to
H
to 
vt 38
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Clarifier Design
In the same time, the particle travels a distance L with a
horizontal velocity vh and therefore
L
t0 
vh

Again Q Where, Q = inflow rate, W = width of the


vh 
HW tank

H L

vt vh
Hvh Q Q
vt   
L LW As Surface Area of Tank

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Clarifier Design
Where, As = WL = Surface Area of the settling zone
 vt is the terminal settling velocity of the slowest-settling
particles that could be removed completely in an ideal
sedimentation basin
 The important design parameter Q/As is called overflow
rate or surface loading rate
 vt is independent of the depth but it is directly related to
the surface area.
 In waste water treatment, the sedimentation tank is fed
with suspension of particles of varying sizes.

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Clarifier Design

Suppose that a particle of terminal velocity vs is introduced


at point A, where vs< vt. This particle will not be removed
during the time provided for settling since it does not
reach the bottom of the settling zone (path AB’)

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Clarifier Design
However, if it is introduced at a distance less than or equal to h
from the bottom, where h = vs to, it will be removed (path A’B).
Hence, the fraction of the particles having settling velocity vs that
can be removed is given by,
v
x t  s

v t
For a given inflow rate Q, where Q  vt A

Of total particles settled, only fraction(1-xt) has the velocity


greater than and equal to vt
The fraction of particles which were removed and have velocities
vs< vt will be xt
v
0 v st dx
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Clarifier Design
The overall fraction (R) removed from the suspension, will be
x
1 t
R  [1  xt ]   vs dx
vt 0
The second term in equation can be determined by graphical
integration of a settling analysis curve, such as the shaded portion
of the given figure with vs<stated value
Fraction of particles

xt
x

vs vt
Settling velocity
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Example (Discrete Settling)

A certain municipality plans to use water from a river. Since


the river is very turbid, pre sedimentation is necessary.
The results of a column test is as follows:
Time 0 60 80 100 130 200 240 420
(min)
Conc 299 190 179 169 157 110 79 28
(mg/l)
What is the percentage removal of particles if the hydraulic
loading rate is 25 m3/m2-day? The column is 4 m deep
x
1 t
R  [1  xt ]   vs dx
vt 0

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Environmental Pollution Control


ETZC362/PEZC411
Prof. Krishna C. Etika
Associate Professor
BITS Pilani Department of Chemical Engineering
Pilani Campus B.I.T.S-Pilani, Pilani Campus

ETZC362/PEZC411 Environmental Pollution Control

Water Pollution

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Example (Discrete Settling)

A certain municipality plans to use water from a river. Since


the river is very turbid, pre sedimentation is necessary.
The results of a column test is as follows:
Time 0 60 80 100 130 200 240 420
(min)
Conc 299 190 179 169 157 110 79 28
(mg/l)
What is the percentage removal of particles if the hydraulic
loading rate is 25 m3/m2-day? The column is 4 m deep
x
1 t
R  [1  xt ]   vs dx
vt 0

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Solution

Time 0 60 80 100 130 200 240 420


(min)
Conc 299 190 179 169 157 110 79 28
(mg/l)

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Solution

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Solution

0.70
those particles which
Fraction Remaining=

0.60
0.50
have Vs<Vt

0.40
0.30
0.20
0.10
0.00
0.00 0.01 0.02 0.03 0.04 0.05 0.06 0.07
Settling Velocity (Vs)

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Solution

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Flocculent Settling

 Takes place when the settling velocity of the particles


increases due to coalescence with other particles.
 A small particle that starts at the surface, end up as a
larger particle when it hits the bottom.
 The opportunity for coalescence increases with the
increase in bed depth, and as a result the particle
removal efficiency depends on both the overflow and the
bed depth.
 Velocity of the floc changes as the size changes
 The path followed by flocculent particles, unlike that of
discrete particles shown in figure:

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Type 2 – Flocculent Settling


Chemical precipitates formed in coagulation and
other destabilization processes tend to agglomerate
while settling as a result of interparticle collisions

→ sizes change

→ shape change

→specific gravity change (as a result of entrapment


of water in interstitial spaces)

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Type 2 – Flocculent Settling

As their size increases, they settle at a faster


velocity
 STOKE’s law not applicable
 impossible to develop a general formula
for determining settling velocities of
flocculent particles.

To determine the settling characteristics


 batch settling column test suspension of
flocculent particles must be performed
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Type 2 – Flocculent Settling


Batch Settling Column Test
 Min . Diameter of column~
about 150 - 200 mm (to
minimize sidewall effects)

 Height of column depth of


the proposed tank

 Sampling port are provided at


equal intervals in height

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Type 2 – Flocculent Settling


Procedure:
1. Suspension to be tested is placed in the column
2. Mixed completely to ensure uniform distribution of particles
3. At time t=0, a portion of the sample is withdrawn in order to
determine the initial concentration
4. The suspension is allowed to settle
5. At periodic time intervals, samples are removed through the ports
located in different heights. For each sample withdrawn at each
depth and for each time, the fraction remaining in suspension at
each time interval is measured
6. Percent removals, Xij = (1- Cij/Co) x 100 = mass fraction
removed (at ith depth at jth time interval)
7. Percent removal lines (Isoremoval lines) are drawn by
interpolation.
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Type 2 – Flocculent Settling


Readings

Isoremoval
Lines

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Type 2 – Flocculent Settling


Total removal at any chosen time = % removal of completely
removed fraction + % removal of partially removed fractions
Initially;
A vertical line from the chosen time is projected upward.
% read at chosen time
= % of particles that are
completely removed.

% read at chosen time


% of particles having Average
Design settling ≥ settling
velocity velocity
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Type 2 – Flocculent Settling

Median lines are drawn between the


percent removal lines

Ave. depth reached read from the


intersection point of vertical line and
drawn median line

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Problem

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Solution

Calculate % removed for each height at each concentration

• Plot the above in the graph and then plot the IRL’s.
• Draw the detention time vertical line at t=105 min

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Solution

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Solution

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Type 3 - Zone Settling

Ultimate
Concentration

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Settling Curve for Concentrated


Suspensions

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Critical Sludge Concentration

The critical concentration, C2 is obtained by bisecting the angle formed by the


tangents to the hindered settling and compression portions of the settling curve

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Design Parameters
Clarifier Area (Ac) Between Ac and At, the larger area
will be the column area!!!
Ac = Q/vh
Q = Overflow rate Slope = vh

Thickening Area (At)


At = Qitu/Ho
Qi = Inflow rate
Time to obtain desired
underflow Concentration (tu)
Final Height of Sludge Zone (Hu)
HoCo = HuCu Ho= Initial height of interface in column
Co= Initial concentration of solids
Hu = (HoCo)/Cu Cu= Desired underflow concentration
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Flotation
 Particles of density very close to that of water are very
difficult to settle in normal sedimentation tanks and take a
long time for separation. This type of operation can be
performed by flotation.

 In this case, the separation can be speeded up by


aerating the effluent whereby air bubbles are attached to
the suspended matter.

 This has the effect of increasing the buoyancy of the


particles; as a result, the particles float to the surface
where they can be readily removed.
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Flotation
 Used in place of sedimentation for finely divided
suspended solids & oil matter
 Used for treating effluents from tannery, metal
finishing, cold rolling & pharmaceutical industries
 Particles having density closer to water, take long time
to settle in sedimentation tanks
 Hence due to buoyancy effect particles float on the top
of liquid
 Hence chemical coagulants such as aluminum and
ferric salts and chemical coagulants are added
 2 methods of flotation are available:
Dispersed air flotation
Dissolved air flotation
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Flotation

Classification of Flotation

1. Dispersed Air Floatation

 Air is dispersed through diffuser or impeller.


 Bubbles are of 1mm diameter and they usually cause
turbulence which breaks up the floc particles.
 Since the floc breaks up , it is usually not a favored
technique.

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Flotation

2. Dissolved Air Flotation

 Air is intimately brought into contact with the waste water


at a pressure of several atmospheres and air is
dissolved.
 Pressure on the liquid is reduced to atmosphere level
through a back pressure valve, thereby releasing micron-
sized bubbles.
 Suspended solids are floated by these minute air
bubbles.

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Secondary Treatment -
Introduction
Primary Treatment: Takes care of those materials that
could be removed by physical or mechanical action.

Organic matter in waste water exists in colloidal and


dissolved form  Primary Treatment Ineffective

Organic matter presence increases the oxygen demand.

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Secondary (Biological)
treatment
Removal of colloids and dissolved organic matter
This operation leads to the natural biodegradation of organic
matter by aerobic bacteria.
The principal requirements of a biological waste treatment
process are an adequate amount of bacteria that feed on the
organic material present in wastewater, oxygen, and some
means of achieving contact between the bacteria and the
organics.
 Role of microorganisms :
 Decomposition of solid waste
 Bacterial population dynamics
 Growth kinetics
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Growth Kinetics- Substrate


Utilization Rate (rsu=dS/dt)
• lag phase: dX/dt & dS/dt ≈ 0
• Exponential growth phase dX/dt & dS/dt ≠0.
• dS/dt and dX/dt obtained just after the
onset of exponential growth phase, one can
compute the yield coefficient Y and the
specific growth rate µ as

The yield coefficient, commonly referred to as the substrate-to-biomass yield, is used to


convert between cell growth rate dX/dt and substrate utilization rate dS/dt.

Y and µ are used to develop microbial growth kinetic relationship.


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Growth Kinetics

rg =

o
-rsu = O

if S << KS First Order w.r.t S

if S >> KS Zero Order w.r.t S

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Activated Sludge Process

Wastewater after primary treatment enters an aeration tank


where the organic matter is brought into intimate contact
with the sludge from the secondary settler or classifier.

This sludge is heavily populated with microorganisms


which are in active state of growth.

The microorganisms (in the aeration tank) utilize the


oxygen in the air and convert the organic matter into
stabilized, low-energy compounds such as NO3, SO4,
CO2, and synthesize new bacterial cells.

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Activated Sludge Process

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Basic Theory and Design of


Activated Sludge Process
 In the activated sludge system, the major design parameter is
the amount of organic matter (food) added relative to the
microorganisms (activated sludge) available.
 This ratio is known as the food to microorganisms (F/M)
ratio.
 Accurate measurement of either F or M is difficult and, hence,
the ratio is usually expressed as the amount of BOD utilized
per unit mass of active biological solids.
 The combination of the liquid and microorganisms in the
aeration tank is known as “Mixed Liquor”, and the suspended
solids are called “Mixed Liquor Suspended Solids” (MLSS).

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Material Balance Around


Activated Sludge System

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Material Balance Around


Activated Sludge System
Assumptions:
(i) No microbial solids (microorganism) in the raw
wastewater influent.
(ii) The influent substrate conc.,So, remains constant with
time.
(iii) The contents in the aeration tank are completely
mixed.
(iv) The system operates under steady state conditions.

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Material Balance Around


Activated Sludge System

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Material Balance Around


Activated Sludge System

Assumptions!!

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Material Balance Around


Activated Sludge System

Substrate Balance

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Material Balance Around


Activated Sludge System

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Material Balance Around


Activated Sludge System
Hydraulic Retention Time Mean Cell residence time
V VX
 c 
Q Q w X r  [Q  Q w ] X e

X = microbial concentration in the aeration tank


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Material Balance Around


Activated Sludge System
e (μm/Y) = k
= max specific
e
substrate
Also, utilization rate

1
K s[  K ]
 d
Se  c
1
Yk  [  K ]
 c
d

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Estimation of Biokinetic
Parameters (Y,k,Ks,Kd)

Y = mx

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Estimation of Biokinetic
Parameters (Y,k,Ks,Kd)

Y = mx

(𝑺𝒐 −𝑺) 𝟏 𝑲𝒅
= +
𝑿𝜽 𝒀𝜽𝒄 𝒀
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Estimation of Biokinetic
Parameters (Y,k,Ks,Kd)
(𝑺𝒐 −𝑺) 𝟏 𝑲𝒅
= +
𝑿𝜽 𝒀𝜽𝒄 𝒀

(1/Y)

(Kd/Y)

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Problem

A completely mixed activated sludge process is to be used to


treat wastewater flow of 500 mg/hr having an soluble BOD5 of
250 mg/l. The concentration of soluble BOD5 escaping the
treatment is 10 mg/l. Given is the following data:
Y=0.5, k=5 day-1, Kd=0.06 day-1, Ks= 100 mg/l and the
condition that the concentration of MLVSS (= X) = 2000mg/l.

Calculate
1. The treatment efficiency
2. The mean cell residence time
3. The hydraulic retention time
4. The volume of the aeration tank

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