Professional Documents
Culture Documents
On
Ashish Traders
Dry Ice Manufacturer and supplier
Submitted by
Mishal Kumar Shukla
Roll No. 15ME19
Submitted to
i
COMPANY CERTIFICATE
ii
CERTIFICATE
This is to certify that this project/ industrial training report entitled “ Quality Control
and Analysis ” submitted by Mr. Mishal Kumar Shukla (Registration No.
1512180175 ) in partial fulfilment of the requirement for the award of the degree of
Bachelors of Technology in Mechanical Engineering to SGT Institute of Engineering
& Technology, Haryana, India is a record of student’s own work carried out under
our supervision and guidance.
To the best knowledge, this project/ industrial training report has not been submitted in
part or full elsewhere in any other University or Institution for the award of any degree
or diploma. It is further understood that by this certificate the undersigned do not
endorse or approve any statement made, opinion expressed or conclusion drawn therein,
but approve the thesis only for the purpose for which it is submitted.
SUPERVISOR
COUNTERSIGNED
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ACKNOWLEDGEMENT
The present work will remain incomplete unless I express my feelings of gratitude
towards a number of persons who delightfully co-operated with me in the process of
this work.
This work was carried out under the supervision of Mr. Vinod Kumar Pandey, Owner,
Ashish Traders, B-18 DDA Market Chowkhandi Tilak Nagar, New Delhi-110018,
India and Mr. Shivendra Singh, Assistant professor, Mechanical Engineering
Department, SGT Institute of Engineering & Technology, Gurgaon, India for which I
would like to express my deepest appreciation and thank for guiding me since it was
assigned, and sharing their insight, experiences, and endless wisdom. I am extremely
grateful and appreciative for all the knowledge and know-how they have given me.
I express and extend my thanks to Dr. Rajan Garg, Professor & Head, Mechanical
Engineering Department, SGT Institute of Engineering & Technology, Gurgaon for his
constant inspiration, painstaking effort and illuminative guidance during the training
period.
My special thanks are due to Mr. Vinod Kumar Pandey, Owner, Ashish Traders, B-
18 DDA Market Chowkhandi Tilak Nagar ,New Delhi-110018, India who taught me
all about perseverance, moral ethics and provided his specialized technical advice and
recommendations, which is really appreciated.
In addition, I am indeed grateful to my beloved parents for creating a positive working
environment, showing me the ropes, their superior guidance, and always being there
for me through the good and bad times.
Thanks, are also especially to Mr. Dinesh Deshwal for interesting discussions and for
being a good and supportive friend.
Greater thanks are due to my dear friends for their endless support.
Place: Delhi
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ABSTRACT
This report gives an overview on quality control process and its use in the various
companies.
Quality Control is an integral part of the production process. The main purpose of
quality assurance and quality control (QA/QC) is to identify and implement sampling
and analytical methods and to decrease the errors into analytical data. Manufactured
products and services are tested to determine if they meet customer standards or not.
Quality control is a service to maintain consistently high standards not for creating the
standards.
For the quality control processes companies use control charts, quality control
software according to the ISO: 9000 standard, visual verification, accuracy
verification and real time quality control.
Quality control and Quality assurance is very important for acquiring customers trust
and market share.
Quality Control process is very useful and the vital and the lifeblood for all the
manufacturing firms. For maintaining the standards they follow statistical process
control (use of control charts), sampling, using of ISO: 9000 standard software,
manual verification and many other modern process. Quality Control not only affects
the quality of the product but also the production cost.
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CONTENTS
Page
CANDIDATE’S DECLARATION i
COMPANY CERTIFICATE ii
CERTIFICATE iii
ACKNOWLEDGEMENT iv
ABSTR v
ACT
CONTE vi
NTS
LIST OF FIGURES
LIST OF TABLES
LIST OF ABBREVATIONS
CHAPTER 1 INTRODUCTION
1.1 Nature of business of the Industry / Institution
1.2 Different products / activities of the Industry /
Institution
1.2.1 dry ice
1.2.2 liquid co2
1.2.3 liquid nitrogen
1.2.4 liquid hydrogen
1.2.5 dry ice blasting
1.2.6 cryogenic blasting
1.2.7 fog machines
1.2.8 gel packs
1.2.9 frozen solutions and services
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2.1.3 quality assurance
2.2 Details about important areas
2.2.1 process of quality control
2.2.2 planning and implementation of quality
control
2.2.3 control charts
2.2.4 approaches
2.2.5 real time quality control
2.2.6 quality system elements and data cycle
2.2.7 standard of digital elevation models in
quality control
2.3 Observations
2.4 Results
2.5 Conclusions
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References
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List of Figures
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List of Tables
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List of Abbreviations
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CHAPTER 1
INTRODUCTION
The company was founded in the year 2006.Today they are one of
the largest supplier and producer of dry ice(solid co2),liquid co2,
liquid nitrogen and other frozen solutions because they are the
most preferred supplier of CO2 and Dry Ice all across Delhi/NCR
and neighbouring states. They have continuously invested for
future requirements and have substantial production, storage and
distribution assets all across the Delhi and can ensure prompt
delivery of any amount or quality of CO2 or Dry Ice that clients
may need. They are particularly preferred by qual ity conscious
clients due to their product and process quality, as well as their
ability to deliver on time and trace online.
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1.2 Different products/activities of the Industry/Institution
Dry ice is the solid form of carbon dioxide. It is used primarily as a cooling
agent. Its advantages include lower temperature than that of water ice and not
leaving any residue (other than incidental frost from moisture in the
atmosphere). It is useful for preserving frozen foods where mechanical
cooling is unavailable.
Dry ice sublimates at 194.65 K (−78.5 °C; −109.3 °F), at Earth atmospheric
pressures. This extreme cold makes the solid dangerous to handle without
protection due to burns caused by freezing (frostbite). While generally not
very toxic, the outgassing from it can cause hypercapnia (abnormally
elevated carbon dioxide levels in the blood) due to buildup in confined
locations.
At pressures below 5.13 atm and temperatures below −56.4 °C (−69.5 °F)
(the triple point), CO2 changes from a solid to a gas with no intervening
liquid form, through a process called sublimation. The opposite process is
called deposition, where CO2 changes from the gas to solid phase (dry ice).
At atmospheric pressure, sublimation/deposition occurs at −78.5 °C
(−109.3 °F) or 194.65 K.
The density of dry ice varies, but usually ranges between about 1.4 and
1.6 g/cm3 (87 and 100 lb/cu ft). The low temperature and direct sublimation
to a gas makes dry ice an effective coolant, since it is colder than water
ice and leaves no residue as it changes state. Its enthalpy of sublimation is
571 kJ/kg (25.2 kJ/mol).
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Dry ice is non-polar, with a dipole moment of zero, so
attractive intermolecular van der Waals forces operate.The composition
results in low thermal and electrical conductivity.
Liquid carbon dioxide is the liquid state of carbon dioxide, which cannot
occur under atmospheric pressure. It can only exists at a pressure above 5.1
atm, under 31.1 °C (temperature of critical point) and above -56.6 °C
(temperature of triple point).The properties of liquid carbon dioxide are the
same as gas carbon dioxide in most parts. As it is a type of liquid phase, it
has viscosity and the viscosity is different at different temperatures. The
history of it is not too long, it starts from the 20th century. As same as gas
carbon dioxide, it can be used in various areas, like using in carbon capture
and storage technology, the extraction of virgin oil paste, fire extinguisher,
coolant and others. In fact, the liquid carbon dioxide may be produced for
very small amount as a homemade experiment by using the dry ice that is the
solid phase of carbon dioxide.
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liquefied nitrogen to be stored and transported over longer time periods with
losses reduced to 2% per day or less.
Liquid hydrogen (LH2 or LH2) is the liquid state of the element hydrogen.
Hydrogen is found naturally in the molecular H2 form.
Dry ice is fast becoming the preferred cleaning solution for a host
of different industries because of its many benefits, primarily
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substantially reducing machine downtime because of its ability to
clean bacteria and micro particles in hot, cold or sensitive area.
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1.2.9 Frozen solutions and services
Commercial solution
1. P H C O N T R O L I N W A T E R A N D P U L P T R E A T M E N T
2. F O O D P R O C E S S I N G I N G E N E R AL
Co2 and Dry Ice is used at almost every step in food processing.
Right from preliminary areas like increased productivity in
greenhouses and humane slaughter of animals, through
intermediary areas of increasing productivity in bakeries, chicken
and other meat processing units (through Cryo grinding and Cryo
mixing), through increasing shelf life and quality of food products
using Modified Atmosphere Packaging and Cryo Freezing, right
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down to providing a flexible and future proof method of
transporting fresh and frozen end products at any user defined
temperature.
3. R E F R I G E R A T E D T R A N S P O R T
4. E N H A N C E D O I L A N D G A S R E C O V E R Y
5. P L A S T I C I N J E C T I O N M O L D I N G
6. C O 2 I N M E D I C A L F I E L D
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Medical and pharma grade CO2 is safe to use in Laproscopic
surgery, cataracts as well as to remove warts. It is also used in
incubation units to promote growth of cells in a controlled
environment.
7. F I R E P R O T E C T I O N W I T H C O 2
8. E N H AN C E C O A L M I N E P R O D U C T I V I T Y
Residential solutions
1.POWER OUTAGE
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Dry ice is an easy and economical way to fumigate and store dry
goods for a long time at home. Put some Dry Ice (without any frost
on it) at the bottom of a food container and then fill the container
with Dry food. As the Dry ice sublimates it replaces all the air
with CO2, without oxygen pests and bacteria in the food can not
survive.. Remember to close the lid only once all the Dry Ice has
completely sublimated and DONT close the lid if there is any Dry
Ice still available in the container. Closing an air tight container
with Dry Ice inside it can be dangerous.
3. M O S Q U I T O A N D B E D B U G T R A P S
Other solutions
1. I Q F
2. C H I C K E N P R O C E S S I N G
Liquid CO2 and Dry Ice is provides a lot of benefits and savings to
Chicken processors. It is used to humanely kill the bird, to reduce
temperature and bacterial contamination during grinding and
blending of mince, to increase shelf life of fresh chicken, to quick
freezing frozen chicken and ready to eat meals, to transport the
end product to supermarkets and other shops.
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3. S P E C I A L E F F E C T S
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Chapter 2
INDUSTRIAL TRAINING
2.1.1 History
In the early 1900s, the beginning of Factory Productions, the final products
were inspected for the purpose of accepting or rejecting the same. During
these times, in his list of basic areas of manufacturing management, F. W.
Taylor, emphasized on quality by including Product Inspection into it.
Radford’s was of the view of involving quality consideration early in the
product design stage and also to connect-together Quality, Productivity and
Costs.
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Control’ concept. At about the same time, Joseph Juran began his `Cost of
Quality’ approach, emphasizing accurate and complete identification and
measurement of Costs of Quality, In the mid 1950s, Armand Fiegen Baum
proposed Total Quality Control which enlarged the focus of Quality Control
from manufacturing to include Product Design.
During the 1960s, the concept of “Zero-defects” gained favor. Philip Crosby,
who was the champion of “Zero defects” concept focused on employee
motivation and awareness. In this decade from 1950 to 1960; quality control
and management became synonymous with the growth of Industrial
Revolution in Japan.
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of manufactured goods. In quality control incoming materials are tested to
make sure they meet the appropriate industry specifications. Quality Control
is an integral part of the production process.
For maintaining the standards they follow statistical process control (use of
control charts), sampling, using of ISO: 9000 standard software, manual
verification and many other modern process. Quality Control not only affects
the quality of the product but also the production cost.
This covers providing evidence for supporting the claim that quality has been
established in work, product or service. For this purpose, suitable standard
operating procedures (SOP’s) are to be introduced for defining a
standardized procedure of doing operations in an effective manner. This
ensures adherence to maximum efficiency and safety requirements of the
clinical research activities that have been performed. Such defined
procedural information assures auditors and regulatory inspectors of
requirements adherence. These SOPs should be sufficiently proliferated
amongst all the individuals involved in the procedure and proper training
should be provided to them. Such planned implementation of procedures is in
complete concordance with the basic PDCA cycle of quality control that asks
quality implementers to plan, perform, measure and take necessary actions as
per the measured data. For this purpose, SOPs are tailored for clinical, pre-
clinical, pharmacokinetics, bio-analysis, regulatory affairs, data management,
drug safety, project management, vendor management, supply chain
management, change control and crisis management.
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2.2 Details about important areas
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Quality is not only a mindset, but also a formalized system. Through strict
documentations and procedures, our engineers and operators maintain
control of quality throughout every step of production.
Our division of the quality control process into three separate processes
ensures that specialized expertise is applied to each stage of our operation.
This system also provides the redundancy necessary to prevent any quality
problem from evading detection
It is the job of the IQC process to conduct inspections and handle quality
problem before the assembly process starts.
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Perform sampling of incoming materials based on the MIL-STD-105E
standard;
Assess dimension, visual and functional inspection of material samples;
Monitor quality control chart of inspected properties and alert engineering
staff of significant deviations;
Continuously enhance the IQC process.
IPQC process governs the quality systems during the assembly process, to
detect and handle problems that may arise as a result of assembly.
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Perform in-process audits to ensure processes are up to standard, and to
identify factors needing improvement.
OQA is the last process before products ship to customers, and hence is
every important to ensure our shipment is defect-free. Numerous
redundancies with IQC and IPQC is performed here to ensure the validity of
previous processes.
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It is also called as statistics. This sampling plays key role in Quality Control
process. Sampling is called as the process of selecting a suitable
sample for study from the whole lot.
1.Single-Sampling-Plan
2.Double-Sampling-Plan
3.Sequential-Sampling-Plan
The types of charts are often classified according to the type of quality
characteristic that they are supposed to monitor: there are quality control
charts for variables and control charts for attributes. Specifically, the
following charts are commonly constructed for controlling variables:
X-bar chart. In this chart the sample means are plotted in order to control the
mean value of a variable (e.g., size of piston rings, strength of materials,
etc.).
R chart. In this chart, the sample ranges are plotted in order to control the
variability of a variable.
S chart. In this chart, the sample standard deviations are plotted in order to
control the variability of a variable.
S**2 chart. In this chart, the sample variances are plotted in order to control
the variability of a variable.
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For controlling quality characteristics that represent attributes of the product,
the following charts are commonly constructed:
C chart. In this chart (see example below), we plot the number of defectives
(per batch, per day, per machine, per 100 feet of pipe, etc.). This chart
assumes that defects of the quality attribute are rare, and the control limits in
this chart are computed based on the Poisson distribution (distribution of rare
events).
U chart. In this chart we plot the rate of defectives, that is, the number of
defectives divided by the number of units inspected (the n; e.g., feet of pipe,
number of batches). Unlike the C chart, this chart does not require a constant
number of units, and it can be used, for example, when the batches (samples)
are of different sizes.
Np chart. In this chart, we plot the number of defectives (per batch, per day,
per machine) as in the C chart. However, the control limits in this chart are
not based on the distribution of rare events, but rather on the binomial
distribution. Therefore, this chart should be used if the occurrence of
defectives is not rare (e.g., they occur in more than 5% of the units
inspected). For example, we may use this chart to control the number of units
produced with minor flaws.
P chart. In this chart, we plot the percent of defectives (per batch, per day, per
machine, etc.) as in the U chart. However, the control limits in this chart are
not based on the distribution of rare events but rather on the binomial
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distribution (of proportions). Therefore, this chart is most applicable to
situations where the occurrence of defectives is not rare (e.g., we expect the
percent of defectives to be more than 5% of the total number of units
produced).
2.2.4 Approaches:
*Quality-reviews
* Auto Software assessment and software measurement.
Planning:
Assessment:
• Data validation and verification
• Data Quality Assessment (DQA)
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2.2.7 Standards for Digital Elevation Models in Quality Control:
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2.3 Observations
Many top management personnel are not aware that relatively simple
techniques like SPC and EPC can be put to use to achieve quantum jumps in
quality improvement and cost reduction.
SPC is a time-tested and effective control scheme used for process capability
analysis and process monitoring. SPC techniques consist mainly of Pareto
Analysis, Scatter Diagram and Regression Analysis, and Statistical Control
Charts.
Pareto Analysis
It is perhaps the most useful tool in the early stages of quality improvement
initiatives. It can be deployed to identify the vital few and screen out trivial
many.
Let us look at the following table on defect counts, taken from the inspection
log of a garment manufacturing unit:
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Table1: Defect counts
Weekly % Cum.
Defect
Total Total %
Missing
57 41.61 41.61
Button
Improper
53 38.69 80.30
Stitch
Length
21 15.33 95.63
Mismatch
Reverse
6 4.37 100.00
Buckle
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Now, what is the conclusion?
Missing buttons and improper stitches contribute 80% of total defects. If the
corrective and preventive actions can be focused on elimination of the root
causes of these two dominant defects from the process, we can easily achieve
a significant reduction in overall defect tally.
They are very useful in the study of inter-relationship between a key process
output variable (KPOV) and a key process input variable (KPIV). If there is a
significant relation between the two, the process output can be controlled
effectively by controlling the process input.
St I St I
S r. m . S r. mp
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l. R p. l. R .
N at % N at %
o e (Y o e (Y)
. (X ) . (X
) )
7. 1 16.
1 16 . 36
1 1 4
8. 1 15.
2 18 . 38
0 2 5
8. 1 18.
3 20 . 40
4 3 9
9. 1 18.
4 22 . 42
5 4 5
11 1 20.
5 24 . 44
.8 5 6
10 1 19.
6 26 . 46
.4 6 8
13 1 21.
7 28 . 48
.3 7 7
14 1 22.
8 30 . 50
.8 8 8
13 1 23.
9 32 . 52
.2 9 6
1 14 2 25.
34 . 54
0 .7 0 4
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Fig (5) scatter diagram
We can predict the value of Product Characteristic (Y) for various values of
Process Characteristic (X) using the following equation:
Y = -0.5011 + 0.4635 X
Consider the data on weight of tablets discussed earlier. You may ask two
interesting questions.
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What amount of adjustment is required NOW to bring the process average to
target value?
Six Sigma:
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3. ANALYSE the data.
The Six Sigma strategy involves extensive use of statistical techniques such
as control charts, design of experiments, response surface methodology etc.
in order to minimize process variations and product / service defects. These
techniques need to be applied in a structured manner.
While reporting the process improvement, Six Sigma teams use certain
numeric values, known as Six Sigma Metrics. The most common metrics are
'Defects per Million Opportunities (DPMO)', 'Sigma Quality Level', and
'Yield'.
It may be noted that the six sigma metrics are just the indicators of process
quality. Sustaining and improving the process performance require process
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monitoring and control schemes such as Statistical Process Control (SPC),
Engineering Process Control (EPC) etc.Six Sigma initiatives aim at reduction
of process variations and defects. SPC and EPC are two important techniques
for achieving these goals. Relatively inexpensive and easy to understand
(requiring minimal support from external experts), it is a feasible proposition
to implement these techniques in any organization.
2.4 Results
RM/PM analysis
Finished Products analysis
In-process Checks
Stability Studies
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Quality Control for API / PM, Finished Products & In-Process Control
is as follows:
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31.
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2.5 Conclusion
In many companies there are quality control departments which controls the
production cost, quality of product, employee’s efficiency and daily work.
Many companies are hiring employees as a quality control manager,
supervisor etc. So the scope of jobs in this department is very good.
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companies are using many advanced technologies for improving the quality
of product and they are recruiting many staves for controlling and assuring
the quality of the product.
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Chapter 3
What I learned from industrial training/my industry
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of dry ice. This is approximately a five minute process. When the block is
solid, it is generally about 2 ft (61 cm) wide and 10 in (25 cm) high,
weighing about 220 lb (100 kg).
6. This block of opaque white dry ice is pushed out of the press and onto a
roller. A pneumatic saw cuts the block in half and the blocks are pushed to
another saw that cuts the smaller blocks yet again. Thus, the single block
made in the dry ice press is now in four pieces, each weighing about 55 lb
(25 kg).
7.The smaller blocks are put into containers that keep the blocks cold so
sublimation is kept to a minimum. If shipped as unwrapped pieces they must
be tightly packed in a container,
generally including four blocks, with very little air allowed inside to reduce
sublimation. If a block is removed during shipping, the other blocks will
quickly begin to dissipate. Many dry ice manufacturers wrap the blocks in
paper using machines (it is wise not to touch the very cold surface) and send
it distributors or wholesalers.
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they meet customer standards or not. Quality control is a service to maintain
consistently high standards not for creating the standards.
Quality control and assurance issues primarily revolve around the grade of
the carbon dioxide used in the manufacture of food grade dry ice. Recently,
the federal government set fairly stringent standards for the purity of carbon
dioxide used in the manufacture of dry ice, causing manufacturers to certify
and test the liquid carbon dioxide used, as well as the purity of the
manufactured product.
Other quality control issues include ensuring that tanks and equipment are
working precisely. If pressure is not properly maintained, the product cannot
be produced. Moving the product quickly and efficiently from cutting to
storage is very important, as dry ice quickly sublimates at room temperature,
thus reducing the weight and price of the salable product. Shipping must
pack the blocks densely to reduce sublimation in transit as well.
1.
The Art Robbins Phoenix protein crystallography dispenser features
accuracy, speed and precision.
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2.
CI-3100 series remote particle sensors detect microscopic particles in
controlled environments and critical processes.
3.
Climet is the world's leading manufacturer of application-driven optical
particle counting instruments.
4.
AUTOTEST 4: fully automatic measuring of weight, thickness, diameter and
hardness.
5.
ETI is a temperature-indicating device and can replace MIG thermometers.
xlviii
6.
Ellab’s TrackSense® Pro high-temperature sensors are ideal for monitoring
processes with extreme heat such as depyrogenation.
7.
The Testo Saver is data logging system offers an extensive range of radio and
Ethernet probes, making it a truly flexible temperature and humidity
monitoring solution
8.
Micromeritics offers an extensive line of particle characterization instruments
for use in fundamental research, product development, quality assurance,
quality control, production, and process control applications.
xlix
continually improve the organization’s ability to produce better products in the
future.
Testing
Unit testing
Integration testing
System testing
No significant chemicals are created in the production of dry ice. Since the
product is made only from carbon dioxide, when the product sublimates the
gases are emitted into the atmosphere. The only detectable waste is
sublimation of the product in block form, which is kept to a minimum.
future
While the use of dry ice in refrigeration and food storage may be
diminishing, its use in other areas holds some promise. As mentioned above,
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house cleaners and machinery operators are interested in the small dry ice
pellets for their ability to bombard a house or machine at high pressure,
remove dirt or other contaminants, and then dissipate into the atmosphere.
Recently a telephone company used dry ice pellets to safely clean sensitive
electronic testing equipment without using dangerous solvents. Car body
repair shops have discovered that applying dry ice to dents in the body can
sometimes eliminate the disfiguration. Also, tests on dry ice blocks advocate
dropping it into gopher holes to eradicate the pests or putting it out in the
backyard to attract mosquitoes in order to keep them away from humans.
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