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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

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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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