Sample Report 1
Sample Report 1
Sample Report 1
Spring 2019
Group 9
Nitric Acid
Final Project Report
Members
Vishal Jajodia : 15B030014
Abhishek Pawan Sharma : 150020010
Shubhangi Chuhadia : 150020072
Hrishav Ranjan : 150020074
Kshitij Chandrachoor : 150020058
This report speaks in detail about the manufacturing of Nitric Acid. Chapter 1 is about
the molecule, its properties and its uses in the industry. Information about different
grades of Nitric Acid is also mentioned in this chapter. We then move on to a market
survey in Chapter 2, which provides an insight into the patterns observed over the past
decade in worldwide nitric acid production and consumption. Top market producers
in both the domestic and global markets were identified and their technology providers
were also identified. We then finalise our new plant location to be Hazira, Gujarat,
based on factors mentioned and discussed in Chapter 2.
In Chapter 3, multiple production routes for Nitric Acid are discussed, varying from
different laboratory methods and the commercially used Ostwald Process. Since the
laboratory methods are not feasible, Ostwald Process is discussed in further detail, ex-
plaining the stages and the operating parameters for each stage. Variations are available
in Ostwald Process, which are useful for plants of different capacities. Processes are dif-
ferentiated on the basis of the operating pressures in multiple stages of the process.
Single Pressure and Dual Pressure processes are explained and compared with each
other. Based on our requirement and multiple factors discussed in this section, we fi-
nally select the Uhde Dual Pressure Nitric Acid Process to be implemented in our new
plant. We choose Thyssenkrupp Industrial Solutions (Uhde GmbH) as our technology
model.
To get a better insight into the Uhde Dual Pressure Nitric Acid Process, we visited
Deepak Fertilisers and Petrochemicals Corp. Ltd.’s Taloja facility. Chapter 4 discusses
this visit in detail. The visit helped us indentify the actual operating parameters for the
Uhde Dual Pressure Process and also helped us gather important information, relevant
to equipment sizing and costing. Based on the information gathered from our visit,
we created our Process Flow Diagram. Chapter 5 discusses the Uhde Dual Pressure
Process, as implemented in the PFD. We also identify the intensive Heat Integration
already available in this well defined process.
ii
Executive Summary iii
Equipment Sizing and Costing is done in Chapter 9. Sample calculations are done
for each major equipment, and subsequent costing calculations are also tabulated, us-
ing costing relations and nomograms for this exercise. The total purchased equipment
delivered cost is used to calculate the total capital investment required for our plant,
which comes out to be INR 894 Crores. Payback Period calculations are also shown in
this section, after total product costs and revenue calculations are carried out. Plant
economics for our process was compared with a recently setup Uhde Plant in Donald-
sonville, Louisiana, USA.
Finally, Environmental Impact Analysis is shown in Chapter 12, detailing the emission
limits in India, process required to bring our emissions within these statutory limits and
the economic impact these additions have on our plant.
Acknowledgement
We would like to take this opportunity to thank our panel members for providing us
constant support and constructive feedbacks, throughout the Design Project exercise.
We would also like to thank Prof. Sanjay Mahajani, Department of Chemical Engi-
neering, IIT Bombay for setting up a visit to the Deepak Fertilisers and Petrochemicals
Corp. Ltd. facility in Taloja, Maharashtra.
At many stages of our project, we acquired guidance from Mr. Amrish Dholakia, En-
gineering Manager, GM - Processes, Thyssenkrupp Industrial Solutions, India. Many
tasks such as Equipment Sizing, Costing, Plant Economics, etc. would not have been
possible without his inputs.
Finally, we would like to express our gratitude to the Overall Supervisors, Nitric Acid
Process Head and the Staff of Deepak Fertilisers and Petrochemicals Corp. Ltd., Taloja,
Maharashtra for helping us understand the intricacies of the Nitric Acid Process during
our visit to their facility.
iv
Contents
Executive Summary ii
Acknowledgement iv
List of Tables ix
1 Nitric Acid 1
1.1 Properties . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
1.2 Uses of Nitric Acid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
1.3 Uses of Intermediates and Byproducts . . . . . . . . . . . . . . . . . . . . 3
1.4 Grades of Nitric Acid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
2 Market Survey 5
2.1 World Consumption Patterns . . . . . . . . . . . . . . . . . . . . . . . . . 5
2.2 World Production Patterns . . . . . . . . . . . . . . . . . . . . . . . . . . 6
2.3 Top Market Producers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
2.4 Technology Providers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
2.5 Location Selection for New Plant . . . . . . . . . . . . . . . . . . . . . . . 9
3 Production Process 11
3.1 Production Routes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
3.2 Ostwald Process . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
3.2.1 Ammonia Oxidation . . . . . . . . . . . . . . . . . . . . . . . . . . 12
3.2.2 Nitric Oxide Oxidation . . . . . . . . . . . . . . . . . . . . . . . . 12
3.2.3 Absorption . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
3.3 Deviations in Ostwald Process . . . . . . . . . . . . . . . . . . . . . . . . . 14
3.3.1 Single Pressure Processes . . . . . . . . . . . . . . . . . . . . . . . 14
3.3.1.1 Medium Pressure . . . . . . . . . . . . . . . . . . . . . . 14
3.3.1.2 High Pressure . . . . . . . . . . . . . . . . . . . . . . . . 14
3.3.2 Dual Pressure Process . . . . . . . . . . . . . . . . . . . . . . . . . 15
3.4 Selection of Final Process . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
4 Industrial Visit 18
4.1 Process Highlights . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
4.1.1 Ammonia . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
4.1.2 Ammonia Filters . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
v
4.1.3 Air Filters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
4.1.4 Ammonia - Air Mixer . . . . . . . . . . . . . . . . . . . . . . . . . 19
4.1.5 Turbine Shaft . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
4.1.6 Reactor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
4.1.7 Boiler . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
4.1.8 Cooler Condenser . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
4.1.9 Absorption Column . . . . . . . . . . . . . . . . . . . . . . . . . . 21
4.2 Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
6 Mass Balance 30
6.1 Sample Calculations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
6.1.1 Reactor - R101 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
6.1.2 Heat Exchangers and Cooler Condenser . . . . . . . . . . . . . . . 32
6.1.3 Absorption Column and Cooler Condenser . . . . . . . . . . . . . 33
6.2 Final Mass Balance Table . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
8 Sensitivity Analysis 41
8.1 Reactor Analysis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
8.2 Heat Exchanger simulated as PFR . . . . . . . . . . . . . . . . . . . . . . 42
8.3 Absorption Column Analysis . . . . . . . . . . . . . . . . . . . . . . . . . 43
vi
10 Plant Economics 57
10.1 Major Equipment Costing . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
10.2 Capital Investment Estimation . . . . . . . . . . . . . . . . . . . . . . . . 58
10.3 Raw Material Cost . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
10.4 Revenue Calculation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
10.5 Total Product Cost . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
10.6 Payback Period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
12 Environmental Impact 73
12.1 Tail Gas Composition and Emission Limits . . . . . . . . . . . . . . . . . 73
12.2 Abatement Technology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
12.3 Tail Gas Post Abatement . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
12.4 Revised Plant Economics . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
12.4.1 Reactor Unit Cost . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
12.4.2 Additional Raw Material Costs . . . . . . . . . . . . . . . . . . . . 76
12.4.3 Additional Revenue Calculation . . . . . . . . . . . . . . . . . . . . 77
12.4.3.1 No CER Revenue . . . . . . . . . . . . . . . . . . . . . . 77
12.4.3.2 With CER Revenue . . . . . . . . . . . . . . . . . . . . . 78
D DWSIM Flowsheet 86
References 88
vii
List of Figures
5.1 Process Flow Diagram for Dual Pressure Nitric Acid Process . . . . . . . 26
5.2 Heat Exchanger Network . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
12.1 EnviNOX
R
Process Variant - 2 . . . . . . . . . . . . . . . . . . . . . . . . 75
viii
List of Tables
ix
11.1 Mathematical Model Results . . . . . . . . . . . . . . . . . . . . . . . . . 65
11.2 Tray Selection Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . 67
11.3 Final Tray Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . 69
11.4 Final Column Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . 72
x
Chapter 1
Nitric Acid
Nitric acid (HNO3 ) is a highly corrosive mineral acid and powerful oxidizing agent. It
occurs in nature only in the form of nitrate salts. The pure compound is a colorless
liquid, but tends to acquire a yellow cast, if stored for long, due to the accumulation of
oxides of nitrogen. Most commercially available nitric acid has a concentration of 55-
70%, being centrally used in the production of nitrogen fertilisers, nylon and explosives.
1.1 Properties
1
Nitric Acid 2
The tabulated data above lists some of the chemical and physical properties of nitric
acid, acquired from PubChem1 . Nitric acid is a nitrogen oxoacid, with a nitrogen atom
bonded to a hydroxyl group and by equivalent resonating double bonds to the remaining
two oxygen atoms, giving the N-atom a +5 oxidation state. This can be seen in the
HNO3 structure shown below :
H O
O N+
O−
Figure 1.1: Uses of Nitric Acid, recreated from Thyssenkrupp Nitric Acid Book [1]
Nitric acid is widely used as an intermediate and its demand majorly depends on the
demand of the end product for which it is used as a raw material. About 90% of nitric
acid is used for on-site consumption and only 10% accounts for retail market. Nitric
Acid is used for following purposes :
1
https://pubchem.ncbi.nlm.nih.gov/compound/nitric_acid#section=
Chemical-and-Physical-Properties
Nitric Acid 3
• About 80% of the world production is used as raw material in the production of
Ammonium Nitrate in the fertiliser industry
• Also used as a raw material in the production of Adipic acid, which is further em-
ployed in manufacturing Nylon-6,6 resins and fibres - widely used in the automotive
industry
• N2 O - Nitrous oxide has significant medical uses, especially in surgery and den-
tistry, for its anaesthetic and pain reducing effects. Its name ”laughing gas” is due
to the euphoric effects upon inhaling it, a property that has led to its recreational
use as a dissociative anaesthetic.
Even though these byproducts find significant uses in multiple sectors of industry, they
are major pollutants when produced in large amounts, with NO and NO2 being the
main causes for acid rains and air pollution and N2 O being a major greenhouse gas,
contributing to the depletion of the Ozone layer and trapping of heat within the atmo-
sphere, and hence, require to be eliminated as per Government of India norms before
being expanded into the atmosphere.
Nitric Acid 4
Market Survey
Due to the rapidly increasing population and reduced availability of land for irrigation,
there is an increasing demand for fertilisers. The use of nitric acid as an intermediate
in the production of ammonium nitrate is a key factor, boosting the production as well
as the consumption of HNO3 . Growing automotive industry drives concentrated nitric
acid market as it is utilized in manufacturing of light weight and strong body parts of
vehicles. Rising demand for synthetic rubbers, elastomers and polyurethane foams in the
automotive industry is anticipated to drive the product demand as well. All the findings
of this section were made after referring Nitric Acid Market Research reports provided
by Research and Markets[2], Grand View Research[3] and IHS Chemical Economics
Handbook[4].
The largest market for nitric acid is the production of ammonium nitrate (AN) and
calcium ammonium nitrate (CAN), accounting for almost 77% of the total world con-
sumption of nitric acid in 2016. World nitric acid consumption has exhibited a steady
upward trend since 2000, with average annual growth rates of 2.0% during 2000-17 [4].
Europe, United States and China account for more than 80% of global demand. Since
2000, the largest increase in consumption has occurred in China, at an average annual
growth rate of 7.3%.
5
Market Survey 6
Figure 2.1: World Nitric Acid Consumption 2017, recreated from [4]
The presence of large agricultural and industrial market in Asia-Pacific is a key factor
responsible for the high growth of the global nitric acid market. Also, the stringent
regulations in regions like North America and Europe regarding the use of ammonium
nitrate based fertilisers are likely to shift the demand to countries in the Asia-Pacific.
Figure 2.2: World Nitric Acid Production 2017, recreated from [2]
Europe and North America account for more than 80% of the global production. In
North America, the United States dominated the market with a revenue share of 70%
in 2017 and it is estimated to continue the trend over the forecast period of 2018-2025.
Robust manufacturing base of chemical, electronics, and automotive industries in the
U.S. is anticipated to supplement the growth of the market in the region.
In Western Europe, Germany represented 15% of the overall revenue in 2017. Lead-
ing chemical companies such as BASF, Bayer and Henkel have their established man-
ufacturing units intended for the production of application-specific bulk chemicals and
speciality polymers in Germany. Aforementioned factors are influencing the growth of
the market in Western Europe positively. Presence of advanced fertiliser manufacturing
facilities in Russia along with abundant availability of raw materials such as ammonia
is projected to be a favorable factor for the market [2].
Ammonia is the key raw material used in the manufacturing of nitric acid. Ammo-
nia production is concentrated mainly in the U.S., China, Eastern Europe and Middle
East because of the availability of large natural gas reserves in these regions.
Market Survey 8
Figure 2.3: Nitric Acid Top Market Producers, recreated with data from [2]
• Borealis of Austria
• KBR of USA
• Technip of France
Option 1 : Ukraine
• High demand for Nitric acid in neighboring countries (Nitric Acid - $300-$400/ton)
• Ease in exporting products and materials (Bordering Black Sea and close to mul-
tiple fertiliser conglomerates)
• Europe being the largest consumer of Nitric Acid provides proximity to desired
market
Option 2 : India
• Large agricultural markets of South East Asia provide huge selling outlets for nitric
acid products like Ammonium Nitrate fertilisers
• Stringent regulations on Nitrate fertilisers in North America and Europe can cause
a shift in the production and selling of these product in and around the Asia Pacific
Market Survey 10
• Proximity to the Hazira Port for importing the raw material and exporting the
final product
• Well established industrial area with great connectivity to the rest of world
Based on the above mentioned factors, the final location for the Nitric Acid plant was
selected to be Hazira, Gujarat, India
Chapter 3
Production Process
This chapter provides details about various production methods for nitric acid, from
laboratory methods to the widely used commercial processes, including their advantages
and disadvantages, and finally concluding with determining the right process for the
plant and its capacity.
2N O + O2 → 2N O2
3N O2 + H2 O → 2HN O3 + N O
All these processes have become obsolete and the only industry used process is the
Catalytic Oxidation of Ammonia by the Ostwald Process and its variants.
11
Production Process 12
Referring to Moulijn et. al. [5], the Ostwald Process involves three steps - (i) Ammonia
Oxidation (ii) Nitric Oxide Oxidation (iii)Nitrogen Dioxide Oxidation
Oxidation temperatures can vary from 750◦ C to 900◦ C. Higher catalyst temperatures
increase reaction selectivity toward NO production. Lower catalyst temperatures tend
to be more selective towards less useful products: nitrogen (N2 ) and nitrous oxide (N2 O).
Nitric oxide is to be used further in our process, whereas nitrous oxide is known to be a
greenhouse gas.
High temperature and low pressure make the reaction more selective towards de-
sired product (NO gas); also owing to the high spontaneity of the reactions, catalytic
bed reactor of residence time of 10−4 to 10−3 seconds is used.
The process stream is passed through a series of heat exchangers and cooler-condensers
and cooled to 50◦ C or less at pressures up to 4 barg. The nitric oxide reacts non
catalytically with residual oxygen to form nitrogen dioxide (NO2 )
This slow, homogeneous reaction is highly temperature and pressure dependent. Oper-
ating at low temperatures and high pressures promotes maximum production of NO2
with a reduced reaction time.
3.2.3 Absorption
The oxidised gas mixture is fed into the bottom of the absorption tower, while a liquid
acid condensate, produced during nitric oxide oxidation, is added at a higher point.
Deionized process water enters the top of the column. Both liquids flow counter-current
to the NOX gas mixture. Oxidation takes place in the free space between the trays,
while absorption occurs on the trays. The absorption trays used are sieve trays.
A secondary air stream is introduced into the column to re-oxidise the NO that is
formed in this reaction. This secondary air also removes NOX from the product acid.
An aqueous solution of 55 to 65 percent (typically) nitric acid is withdrawn from the
bottom of the tower. The acid concentration depends upon the temperature, pressure,
number of absorption stages, and concentration of nitrogen oxides entering the absorber.
Referring to Moulijn et. al. [5], we found out that the principal design variables for the
ammonia oxidation and subsequent stages of the plant are temperature, pressure and
gas flow rate, and their effects on the process efficiency is tabulated below:
According to Thiemann et. al. [6] and Thyssenkrupp Nitric Acid Book [1], classification
of plants is done on the basis of pressure in the oxidation and absorption stages:
This type of nitric acid plant operates at around 4–5 bars abs. It can produce up to
700 tonnes/day using a single combustion and a single absorption tower and around
1000 tonnes/day by adding another absorption tower. Using this pressure enhances the
oxidation step (NO to NO2 ), but reduces the productivity of the final absorption stage.
Pressure of around 8–12 bars abs is used. This high pressure forces the nitrogen dioxide
gas into water. And thus, a single absorption tower is sufficient to produce 900 tonnes/-
day of nitric acid. The higher pressure means that other equipment like the burner unit,
Production Process 15
piping can be made smaller so the plant occupies less space, making the initial capital
investment less.
Lower pressure for ammonia oxidation and higher pressure for absorption is favourable.
The dual pressure plant uses two different pressures, a lower pressure for the oxidation
step and higher pressure to optimize the absorption. This type of plant can produce up
to 1600 tonnes/day of nitric acid using single combustion and absorption unit. Lower
pressure for the oxidation unit also reduces the catalyst cost.
The points considered while finalising the actual process to be utilised in the plant are:
• Variable Costs
• Capacity
• Catalyst Life
• Environmental Impact
• Electric Power
In accordance with the above mentioned points, the following comparisons1 are docu-
mented and are also an industry-wide practice:
1
All comparisons are per tonne Nitric Acid (100%)
Production Process 16
• The dual pressure process provides larger capacities (upto 1600 tpd in single train
configuration) with relatively lower variable costs, when compared to the mono
pressure processes (upto 900 tpd for high pressure, upto 700 tpd for medium
pressure - in single train configuration), which require larger variable costs.
• Due to a lower load on the burner, the dual pressure process also provides with a
longer operation time for a given bundle of catalyst gauzes(> 6–8 months), when
compared to the other available processes(upto 6 months). This effect can be
seen directly on the total catalyst losses for dual pressure process (0.03g/t of nitric
acid produced) when compared to the mono pressure processes (0.04g/t nitric acid
produced for medium pressure process and 0.08g/t nitric acid produced for high
pressure processes respectively)
• All processes can easily provide the required nitric acid concentration (≈ 60% wt)
• When comparing all the alternatives, the dual pressure process requires the least
amount of electric power per ton nitric acid produced (8.5 kWh), followed by
medium pressure (9.0 kWh) and high pressure (13.5 kWh)
With reference to average plant capacities using dual pressure process, keeping in mind
the demand for nitric acid, which is growing at a rate of 3-5% annually, and the incre-
mental production of the plant i.e. 70% in the first year, 80% in the second year and
so on, the final plant capacity has been decided to be kept at 1500 TPD of 62% wt
nitric acid (942 TPD in terms of 100% wt nitric acid)
Keeping in mind the desired production from our plant, the final route for the produc-
tion of nitric was chosen to be the Dual Pressure Process, with medium pressure
ammonia oxidation over Pt–Rh catalyst and high pressure absorption operations.
Production Process 17
• Abu Qir Fertilisers and Chemical Ind. Co., Abu Qir, Egypt - Capacity - 1850 TPD
(As an industry standard, plant capacities are displayed in terms of 100% wt nitric acid)
Hence, our final plant details are as follows: 1500 TPD of 62% wt (942 TPD in terms
of 100% wt nitric acid) nitric acid plant, using the Uhde Dual Pressure Process, set
up in Hazira, Gujarat, India.
Chapter 4
Industrial Visit
In order to gain a better understanding of the selected process and to aid selection
of parameters and equipment, a visit to Deepak Fertilizers and Petrochemical Corp.
Ltd.(DFPCL) [7] was made on February 6, 2019.
Total Nitric Acid Capacity: 1400TPD
4 nitric acid plants:
2 mono high pressure plants (300TPD each, set up in 1996)
1 mono medium pressure plant (350TPD, set up in 2000)
1 dual pressure plant (Uhde Dual Pressure Process, 450TPD, set up in 1975, Denmark,
recommissioned in 2010, India)
The weak nitric acid (59.2% wt) produced here is used further for ammonium nitrate
production and concentrated nitric acid (98.5%wt) is sold separately. Since the dual
pressure plant is recommissioned, it has a few added features to adjust to the tempera-
ture and pressure in India. For example, the compressors used are designed for a lower
air temperature (Denmark) whereas the ambient air temperature in India is high. Hence,
air chillers are added to reduce the temperature of the air to 20◦ C before compression.
18
Industrial Visit 19
4.1.1 Ammonia
Deepak Fertilisers has a separate plant for ammonia production which usually meets the
nitric acid requirement. An alternate of sourcing ammonia externally during off days is
also in place. The ammonia obtained is stored in a cylindrical storage refrigerated tank
at -33◦ C and 1 atm pressure.
Ceramic tubes are used to filter oil, water and other impurities from ammonia. The
ammonia feed enters radially, is filtered and exits through the axis.
The air is compressed to 5 bar abs using a centrifugal compressor. Primary and Sec-
ondary Filters are used to filter out particulate matter before compression. These filters
are made of Stainless Steel and present in huge numbers, incorporated with the cooling
network inside the filter rack.
Mixer used in the industry is a Stainless Steel Static Mixer, where both the gas streams
are intermixed, entering perpendicular to each other.
Industrial Visit 20
A single steam turbine is used to rotate a shaft which is connected to a series of compres-
sors and expanders. HP steam is used to rotate the turbine at 7000 RPM. The turbine
shaft is used to rotate a centrifugal compressor, which compresses air from atmospheric
pressure to 5 bar abs pressure. The second equipment on this shaft is an expander; it
reduces the pressure of the tail gas from approximately 12 bar abs to 1 atm. A gear
(1:14) is used after that to increase the rotations per minute for the NOX compressor.
The energy from steam and tail gas is efficiently used to run the compressor shafts.
Figure 4.2: Turbine Shaft Structure, as seen in the DFPCL Dual Pressure Plant
4.1.6 Reactor
A shallow bed reactor with 8 gauzes of 95-5 Pt-Rh is used. The reaction is highly
exothermic and takes place at 890◦ C. For the start-up of the process, hydrogen gas
is burned to raise the temperature of the gauzes (around 8 cylinders of hydrogen are
kept in the inventory (4 for main use + 4 for extra backup)). After the reaction starts,
the heat of the reaction is sufficient to maintain that temperature. 96% of ammonia
is converted in a single pass. Catchment gauzes of Palladium are provided to capture
catalyst chipped off with outgoing stream.
4.1.7 Boiler
The product stream leaving from the reactor exits at 890◦ C. This steam is to be cooled
before adding to the absorption column. And therefore, a series of heat exchangers and
cooler condensers are added. A waste heat boiler is attached just below the reactor
setup, with hot water flowing through the tube side. In the boiler, the temperature of
the process stream is reduced from 890◦ C to 410◦ C. High pressure steam is produced
while cooling the process stream, which is used to run the steam turbine.
Industrial Visit 21
There were three cooler condensers used instead of the conventional two to reduce the
load on condensers.
Figure 4.3: Nitric Acid Cooler Condenser Structure, provided by DFPCL [7]
A sieve tray counter-current absorption column (42 m in height) absorbs incoming NOX
into a deionised makeup water stream to form 59% w/w Nitric Acid as bottom product.
NO2 absorption in water occurs on the tray whereas NO oxidation to NO2 occurs between
the trays. Cooling water coils at each stage are used to absorb the heat released by
reactions.
4.2 Conclusion
The process studied from literature and the one being used in the plant was very sim-
ilar. Doubts regarding the type of equipment used, exact conversions and temperature
pressure conditions were solved by this visit. The size of the DFPCL Dual Pressure
Plant was comparatively low and with reference to findings from the visit, changes were
made to scale up the plant capacity for verification with our new plant data.
Chapter 5
This chapter showcases the Process Flow Diagram (PFD) for the Dual Pressure Nitric
Acid Process. The PFD was made with inputs from Moulijn et. al. [5], Thiemann et.
al. [6] and DFPCL Staff [7]. The PFD was drawn using an online flowsheet drawing
software Draw.io1 .
The final PFD with the stream table for our Dual Pressure Nitric Acid Process is avail-
able in Appendix A. All pressures mentioned are in bar abs, unless specified otherwise.
• Air (stream-1) is pumped into the plant at ambient conditions (1 atm, 35◦ C),
entirely by the suction force provided by the centrifugal compressor, C101. The
Air is filtered using primary and secondary Air Filters in F101 and fed to the
compressor (stream-1A).
• The compressor C101 is used to increase the pressure of the air feed to 5 bar, also
causing an increase in the temperature to 240-250◦ C. Stream-1B is split into 2
parts, 85% going into the reaction mixture (Primary Air, stream-1C) and the rest
(Secondary Air, stream-1D) is utilised in the bleaching column, B101.
1
https://www.draw.io/
22
Process Flow Diagram 23
• Liquid Ammonia from storage is pumped into the plant at -33◦ C and 19 bar, into
Evaporator E101 by a Centrifugal Pump, numbered stream-2. In the Evaporator,
Ammonia is converted to vapor and further superheated to 70◦ C with the help of
LP Steam (4-5 bar, 150◦ C) in the upper section of Evaporator E101.
• Ammonia Filter, F102 is utilised to filter the superheated Ammonia vapor (stream-
2A) of the small amounts of impurities inherent to the Ammonia feed (oils, chlorine,
etc.).
• The superheated ammonia vapor and the compressed air stream are mixed in a
static mixer, with ammonia to air ratio being 1:9 by volume, giving us stream-3,
at 5 bar, 220-230◦ C.
• Stream-3 is fed into the reactor, R101, which is a shallow bed reactor, with around
8-10 catalyst gauzes, made up of 90% Pt and 10% Rh. Hydrogen gas is utilised
to heat up the gauzes to the required temperature at startup; once the reaction
starts, the heat of the reaction is sufficient to sustain the reaction.
• The catalyst is highly selective, giving a conversion of 96% for Ammonia into
Nitric Oxide, with stream-4 exiting at a temperature of 890◦ C, consisting mainly
of Nitrogen and Oxygen from Air feed and Nitric Oxide formed via Ammonia
oxidation. Some small amounts of N2 O is also formed (1200 ppmv) due to the
occurence of the side reaction.
• The high heat of reaction is used to make steam and heat other streams throughout
the plant. Waste Heat Boiler attached to the reactor is used to produce HP Steam
(40 barg), which is used to run the steam turbine, using the energy to run the
compressors. Shell and Tube Heat Exchanger, HE102 is used to heat the tail gas
(stream-10) coming from Absorption Column to facilitate the abatement process,
and HE103 is an Economiser, used to preheat the water to boiler to 80◦ C, which
results in the temperature of stream-5 to drop to 185◦ C.
• This decrease in the temperature leads to the oxidation of Nitric Oxide to Nitrogen
Dioxide (stream-6), with the conversion of the reaction increasing with a decrease
in the temperature.
• Cooler Condenser-1 (HE104), is used to cool the stream further, condense water
and nitric acid and separate them out for further processing. The temperature
Process Flow Diagram 24
of the outlet streams (7 & 8) is around 50◦ C. This drop in temperature allows
Nitric Oxide to oxidise to Nitrogen Dioxide at a much higher conversion rate when
compared to the previous two heat exchangers (HE102 & HE103).
• The Nitric Acid solution in the condensate of the Cooler Condenser-1 (HE104),
with a concentration of about 35-40% wt Nitric Acid by weight, is then pumped
(stream-7) to the Absorption Column (A101) to increase the Nitric Acid concen-
tration in the solution.
• The vapor outlet of HE104, stream-8, mainly consisting of NOX gases, is passed
through the NOX Compressor, C102, elevating the pressure of the stream to 12
bar and the temperature to around 260◦ C.
• C102 outlet, stream 8A, is the fed to Cooler Condenser-2 (HE105), where process
similar to that in Cooler Condenser-1 (HE104) occurs, providing us with more
weak Nitric Acid condensate, which is mixed with HE104 condensate and pumped
to the Absorption Column. Stream-9 coming out of HE105 is also fed to the
Absorption Column (A101).
• The Absorption Column (A101), has 35-40 stages, with the NOX gases (stream-9)
fed at the bottom-most stage, process water (stream-12) fed at the top-most stage,
acid condensate from the Cooler Condensers (stream-7) fed to an intermediate
stage (stage 13) and cooling water coils at every stage throughout the column to
maintain the column at a reduced temperature.
• Since the Absorption Column is operated at an elevated pressure (12 bar), absorp-
tion efficiency is increased, which results in fewer NOX emissions.
• Inside the column, Nitric Oxide oxidation to Nitrogen Dioxide occurs between
stages in the vapor phase, and absorption of Nitrogen Dioxide into water and the
formation of Nitric Acid from the absorbed Nitrogen Dioxide occurs in the liquid
phase on the sieve trays of the column.
Process Flow Diagram 25
• Top outlet of the column is called Tail Gas (stream-10), with NOX concentration
in the order of 550ppmv. Stream-10 is then preheated in HE106 using secondary
air (stream-1D) and further heated in HE102 using stream-4 and sent to the NOX
abatement process where it is expanded to provide 65% of the energy required to
run the compressor shafts and then vented into the air.
• Bottom outlet of the column (stream-11) is called Red Fuming Nitric Acid, due to
the red color imparted by the dissolved Nitrogen Dioxide.
• Stream-11 is fed to the Bleaching Column, B101, where the secondary air strips
away the Nitrogen Dioxide, resulting in a clear, colorless 62% wt. Nitric Acid
Solution. The product acid (stream-14) is further cooled and stored in cylindrical
storage tanks. The bleaching air is mixed with the NOX compressor inlet and
again fed to the absorption column, to ensure lower NOX emissions in the tail gas.
• The Tail Gas (stream-10) from the column is first preheated to 130◦ C, using the
secondary air to be fed to the bleaching column, in Tail Gas Preheater, HE106,
and further heated to 350◦ C in HE102.
• The tail gas can now be fed to the abatement process, where the NOX and N2 O
concentration is reduced to below 40 ppmv. Ammonia and Propane are mixed
with the tail gas as it enters the abatement unit.
• After the abatement, the tail gas is expanded in the tail gas turbine, EX101,
providing around 65% of the energy to drive both the air and NOX compressors.
Once expanded, the tail gas is vented into the air via Stack.
Process Flow Diagram
Figure 5.1: Process Flow Diagram for Dual Pressure Nitric Acid Process
26
Process Flow Diagram 27
Nitric Acid Process is one of the world’s oldest and most researched industrial production
process. Hence, the intense amount of research that has gone into this process has led to
the latest iteration of the process flow to take shape, that we have incorporated into our
PFD. This process is highly integrated, from heat to energy. There was no requirement
to do a detailed heat integration study as the entire process has been well researched
and provided with the ample amount of heat and energy integration required to make
any nitric acid plant profitable in the smallest period of time.
The process has one main hot stream - Reactor outlet gas, coming out at a temperature of
890◦ C. It has to be cooled down to a temperature of 50◦ C before it enters the absorption
column. The first heat exchanger after the reactor is the Waste Heat Boiler, attached
directly to the reactor burner head. The gas flows through the shell side of this shell and
tube heat exchanger, with boiler feed water passing through the special boiler tubes,
made out of SA 192 and SA 213 - T12 Grade, to account for the evaporation and super
heating of the High Pressure steam produced in the boiler. This causes the temperature
of reaction mixture to drop to 427◦ C.
This HP Steam is used to run the Steam turbine used to run the common shaft, which in
turn drives the compressors. The LP Steam from the turbine is then used to superheat
the evaporated ammonia to a temperature of 70◦ C. Ammonia evaporation utilises cooling
water to evaporate the liquid ammonia. The water in turn is cooled down to 7◦ C, where
it can be used as chilled water, used for cooling the top section of the absorption column.
After the Waste Heat Boiler, the NO gas is further cooled down to 300◦ C in the Tail
Gas Heater, by utilising the cold tail gas emanating from the absorption column. This
heats the tail gas (stream-10) to 350◦ C, temperature required by the abatement unit
to function properly. The NO gas is further cooled down to 185◦ C in the economiser.
The cooling stream here is the boiler feed water used in the Waste Heat Boiler, whose
temperature is increased from 40◦ C to 80◦ C.
The next two shell and tube heat exchangers are the largest heat exchanger in the plant.
The cooler condensers are utilised to cool down the reaction gases to 50◦ C, which helps
in forming the acid condensate. Cooling water is used in both the cooler condensers,
one before and one after the NOX compression.
Process Flow Diagram 28
The tail gas coming out of the Absorption Column is reduced in order to meet the
government norms for NOX emissions. The abatement process requires temperatures of
around 350◦ C (stream-15), and hence the tail gas, coming out at 10◦ C, is first preheated
in the Tail Gas Preheater to 130◦ C (stream-10), with the help of the hot secondary air
(stream-1D) used in the bleaching column, and further heated in the Tail Gas Heater
(HE102) as mentioned in previous points. Once abated, the tail gas is used to drive a
turbine, which provides around 65% of the power required to drive the air and NOX
compressors (C101 and C102).
This integration is followed in all Dual Pressure Nitric Acid Processes, with slight varia-
tions in stream temperatures for processes from different technology providers. The net
utility data is produced in a tabulated form below:
Utility Amount
Utility Required Net Amount Required
Produced Produced
Electricity 2465 kW
Cooling Water 0.437 MGal/hr HP Steam
26680 kg/hr
Make Up Chilled Water 0.0134 MGal/hr (40 barg)
LP Steam 12600 kg/hr
The above mentioned Heat and Energy integration leads to the following heat exchanger
network:
Process Flow Diagram
Mass Balance
This chapter provides a look at the mass balance performed on the process, with inputs
from Ray et. al. [8], source of the reference being DFPCL [7]. Some sample calculations
are also provided for some major equipment taking 100kmol/hr Ammonia as the basis.
All values were scaled up for the desired plant capacity.
Air is passed through a combination of primary and secondary filters and compressed
to 5 bar abs (240◦ C) from ambient conditions. Ammonia is evaporated from sub-zero
temperatures using water, passed through a preheater to raise the temperature to 70◦ C
and filtered to remove oils and particulate matter using the ammonia filters. Ammonia
& air are mixed in 1:9 ratio and the mixture enters the reactor at 230◦ C.
Reactor residence time is in few milliseconds where Pt-Rh catalyst provides the site for
reaction. Reaction occurs at 890◦ C which is maintained by the high exothermicity of
the reaction.
Main Reaction:
30
Mass Balance 31
96% ammonia conversion is towards main reaction producing NO and the rest towards
side reactions:
Ammonia entering reactor = 100 kmol
NO formed: 100*(96/100) = 96 kmol
Required O2 for main reaction: 96*5/4 = 120 kmol
H2 O formed in main reaction: 96*3/2 = 144 kmol
Side Reaction 1:
Side Reaction 2:
Similar calculations are made for all other equipment using their conversions and desired
outputs.
The primary reaction that takes place next is the oxidation of nitric oxide to nitrogen
dioxide.
2N O(g) + O2 (g) → 2N O2 (g), ∆H = −114kJ/mol
This reaction takes place when the process gas is passed through a series of heat exchang-
ers and the conversion increases with reducing temperature. The process gas first passes
through Tail Gas Heater-1, where its heat is used to preheat the tail gas exiting from
the absorption column. It further passes through an economizer, used to preheat boiler
feed water and then through cooler condenser-1. By this point, the temperature of the
process gas comes down to 50◦ C, which is favourable for high nitric oxide conversion.
Simultaneously, water formed in the ammonia oxidation condenses, thereby dissolving
NO2 and forming HNO3 in small amounts as condensate.
The conversion of NO in Tail gas heater-1 is ≈ 15%, in the economiser is ≈ 27% and
the concentration of acid condensate is ≈ 38%. These figures are similar to the DFPCL
data [7].
NOx
Reactor HE102 HE103 Acid
Comp.
Component Outlet Outlet Outlet Condensate
Inlet
(kmol/hr) (kmol/hr) (kmol/hr) (kmol/hr)
(kmol/hr)
O2 66 59 48 20 0
N2 712.5 712.5 712.5 712.5 0
H2 O 150 150 150 0 138
N2 O 0.5 0.5 0.5 0.5 0
NO2 0 14 36 56 0
NO 96 82 60 16 0
HNO3 0 0 0 0 24
The process gas (known as NOX gas) is compressed to 12 bar abs (260◦ C) and fed to
cooler condenser 2. The gas stream is then fed to the absorption column at the bottom
and acid condensate from cooler condenser 1 is fed at the middle of the column for
further concentration. Process water added at the top of the column at 10◦ C absorbs
the NO2 forming HNO3 and NO formed as a side product gets oxidised back to NO2 by
excess air added to the column.
The acid leaving the column from the bottoms is 55%-60%wt which then passes through
the bleaching column to be stripped off of dissolved NOX gases. The tail gas leaving
from the tower of the tower is further sent for NOX abatement process to bring down
the NOX content to permissible levels. The basis for calculations on the column was the
empirical concentration of different NOX gases in the tail gas as 550ppmv.
Cooler
Acid Nitric Acid
Condenser 2 Tail Gas
Component Condensate Bottom
Outlet (kmol/hr)
(kmol/hr) (kmol/hr)
(kmol/hr)
NH3 0 0 0 0
O2 12.5 0 19.5 0
N2 713 0 808 0
H2 O 0 138 0 202.54
N2 O 0.5 0 0.5 0
NO2 71 0 0.06 7.82
NO 1 0 0.6 0
HNO3 0 24 0 94.42
Above calculations were scaled to our desired production of 1500TPD of 62% Nitric Acid
Solution, providing us with the following results 1 :
1
All values are in kg/hr
Mass Balance
Line No. Stream Comp. Phase NH3 O2 N2 H2 O N2 O NO2 NO HNO3 CO2 C3H8 Total Pressure(bar abs) Temperature (◦ C)
1 Air feed g 0 43519 145541 0 0 0 0 0 0 0 189060 1 35
1C Primary Air g 0 39005 128387 0 0 0 0 0 0 0 167391 5 240
1D Secondary Air g 0 4514 17154 0 0 0 0 0 0 0 21669 5 240
2 Ammonia Feed l 11003 0 0 0 0 0 0 0 0 0 11003 1 -33
2A Evaporated NH3 g 10963 0 0 0 0 0 0 0 0 0 10963 5 70
3 Reactor Inlet g 10963 39005 128387 0 0 0 0 0 0 0 178355 5 230
4 Reactor Outlet g 0 13570 128658 17412 142 0 18573 0 0 0 178355 5 427
5 HE102 Outlet g 0 12125 128658 17412 142 4153 15865 0 0 0 178355 5 300
6 HE103 Outlet g 0 9856 128658 17412 142 10680 11608 0 0 0 178355 5 185
7 Acid Condensate l 0 0 0 16019 0 0 0 9751 0 0 25770 12 50
8 NOx Comp. inlet g 0 8591 145812 0 142 18932 3096 0 0 0 176573 5 50
8A NOx Comp. Outlet g 0 8591 145812 0 142 18932 3096 0 0 0 176573 12 260
9 Absorption Inlet g 0 7043 145812 0 142 23382 193 0 0 0 176573 12 50
10 Tail Gas g 0 3307 145812 0 142 18 58 0 0 0 149336 12 130
11 Absorption Outlet l 0 0 0 23816 0 2320 0 38858 0 0 64993 12 50
12 Process Water l 0 0 0 11987 0 0 0 0 0 0 11987 12 10
13 Bleaching Air g 0 4514 17154 0 0 2320 0 0 0 0 23988 5 80
14 Nitric Acid Pdt l 0 0 0 23816 0 0 0 38858 0 0 62673 5 50
15 Mixed Tail Gas g 40 3307 145812 0 142 18 58 0 0 0 149376 12 350
16 Reduced Tail Gas g 0 3292 145966 87 2 1 2 0 42 0 149391 12 350
17 Tail Gas Out g 0 3292 145966 87 2 1 2 0 42 0 149391 1 35
18 Reducing Ammonia g 40 0 0 0 0 0 0 0 0 0 40 12 350
19 Propane g 0 0 0 0 0 0 0 0 0 15 15 12 350
34
Chapter 7
We employed the DWSIM Chemical Process Simulator for process simulations of the
Nitric Acid plant. DWSIM is a multiplatform, CAPE-OPEN compliant chemical process
simulator featuring a rich graphical interface with many features previously available
only in commercial simulators. DWSIM being a free and open source software provides
everyone with the opportunity to simulate process free of cost. The direct benefit of this
is that DWSIM can directly replace commercial simulators like ASPEN or can at the
least be used for multiple simultaneous test-simulations in companies where there is a
shortage of ASPEN licenses. The simulations helped us not only validate our data from
linear mass balance and the visited DFPCL plant, but also optimize process operating
conditions.
Our DWSIM flowsheet is available online on the FOSSEE Flowsheeting Project portal
- https://dwsim.fossee.in/flowsheeting-project/dwsim-flowsheet-run/335
35
DWSIM Flowsheet Simulation 36
Ammonia oxidation reaction in presence of Pt-Rh catalyst is highly selective and occurs
almost instantaneously, with residence time in the order of 10-4 - 10-3 seconds. Hence,
the available Conversion Reactor is used as an equivalent for the Shallow Bed Reactor
for optimised temperature and pressure conditions, giving a conversion of 96% for the
desired reaction. It is also assumed that almost all ammonia is consumed in the reactor,
either in the main reaction or in one of the side reactions.
The instantaneous nature of the reactions call for a millisecond reactor, which is why it
is difficult to use a kinetic model of this reaction in the simulation of the reactor. Only
one of the side reactions is considered in the DWSIM Flowsheet.
In this step, the temperature of the stream is reduced which leads to the kinetic ox-
idation of NO to NO2 to move in the forward direction. Since the heat exchangers
cannot be modelled to include a reaction in them, plug flow reactors are used instead.
DWSIM PFRs give us the ability to calculate the heat duty for our required process,
while enabling us to model kinetic reactions, satisfying our requirements of reactive heat
exchangers.
2N O(g) + O2 (g) → 2N O2 (g), ∆H = −114kJ/mol
DWSIM Flowsheet Simulation 37
NO Oxidation is a third order reaction, with reaction rate and constant as,
2
Rate = 2kp CN O CO 2
530
logkp = + 7.09
T
Hence, the Arrhenius parameters required become, A = 1200 and E = -4406.42, values
taken from Tsukahara et. al. [9]
Water formed in the ammonia oxidation reaction reacts with absorbed NO2 to form
HNO3 . Since the reaction is mass transfer controlled, the kinetics involved in this
reaction are very difficult to model and therefore a simpler alternative used for this
reaction was to model an equilibrium reactor, with the equilibrium reaction,
3N O2 (g) + H2 O(l)
2HN O3 + N O(g), ∆H = −75kJ/mol
with Kp being the equilibrium constant, given by Thiemann et. al. [6] as,
logKp = −7.35 + 2.64/T
Cooler Condenser is modelled using a PFR to take into account the NO Oxidation,
followed by an Equilibrium Reactor to model the Nitric Acid formation and a Gas-
Liquid Separator to produce Acid Condensate and NOX gas.
The separated streams are sent to the absorption column. In the absorption column,
the NO2 is absorbed in water and reacts to form HNO3 and NO, which is again oxidised
to form NO2 , and so on. Modelling of a reactive absorption column was done using a
ChemSep column, with the specified reactions used in the unit. Issues propped up as
DWSIM Flowsheet Simulation 38
the desired conversion couldnt be achieved, hence a different approach was used. The
column was divided into two parts - Absorption and Reaction. A Simple Absorber was
used to facilitate NOX absorption into water, followed by a series of reactors to model
the NO Oxidation and Nitric Acid formation reactions. Two recycle streams were used
in this part, to recycle back the unconverted gases, to achieve the given conversions and
concentrations.
7.2 Comparisons
** Note - All flow rates mentioned in the tables below are in kg/hr
DWSIM Flowsheet Simulation 39
Sensitivity Analysis
The above results are produced for the operation of the reactor at 4 barg pressure. To
get high values of conversion for our reaction, the optimum temperature at which the
reaction should be done is between 860 - 920◦ C. The highest possible conversion at 4barg
is 96%, which occurs when the reactor is operated at 890◦ C. Hence, 890◦ C was chosen
as the operating temperature of the Ammonia Oxidation Reactor.
41
Sensitivity Analysis 42
The above analysis compares the Nitric Acid Solution Flow rate and Concentration as
a function of extra added air. The minimum amount of extra O2 required is 1kg/s
which provides us with the best results, the selected O2 rate was set at 1.25 kg/s, which
Sensitivity Analysis 44
provided us with the least amount of NOX in the tail gas as well. The mentioned
comparisons are for the said extra O2 values, which are obtained from the secondary
air, and can be manipulated using the split ratio and intake of air.
Another important parameter to take care of while designing the absorption column
is the total pressure drop across the column. Since we want to use the pressurised tail
gas to generate energy, low pressure drops are desired. The pressure drop is a function
of the diameter of the column, which in turn is a function of the tray spacing. Lower
spacing (0.3-0.6 m) require smaller diameters and hence a relatively lower capital cost,
but cause a larger pressure drop. Whereas larger spacing (1.0-1.2 m) require larger
diameters but cause smaller pressure drops, helping us reduce our operating costs by
providing higher amounts of energy. Hence, a diameter of 5 m, with spacings of 1.0 m
in the bottom part (trays 1-13) and 1.2 m in the top part (trays 13-36) is chosen for the
column.
Chapter 9
In this chapter, we size the major equipments used in the plant and also estimate the
cost of each of the equipment. They are listed in the following sections. The following
data is used in the cost estimation:
• Dollar to INR = 70
• Direct and Indirect Costs in FCI are calculated using percentage normalisation
from Peters et. al. [10]
• Equipment Cost is estimated using Nomograms from Peters et. al. [10] and Cost
relations from Walas et. al. [11]
• All equipment are mapped to the average 2018 Cost Index - 603.1 (As of Dec 18),
data acquired from ChemEngOnline Website[12]
The Ammonia Oxidation Reactor is a shallow bed reactor, with a burner head and 90-10
Pt-Rh gauzes as its main parts. Since Pt-Rh Gauzes have a lifetime of 6-8 months, only
45
Equipment Sizing and Costing 46
first 24 months of the catalyst gauzes will be capitalised and the rest will be incorporated
into the Operating Costs. The burner head is a pressure vessel head, with a conical shape
and operating pressure of 5 bar abs. Since the burner head doesnt come under the direct
heat of the reaction gases (890◦ C), we dont require any special material of construction
for the said equipment.
The diameter of the gauzes and that of the burner head are calculated using the following
data provided by Krupp Uhde[13]
3. Platinum required for given Nitrogen - 320g Pt/Tonne per day Nitrogen
NH3 consumed = 3.056 kg NH3 /s = 0.17974 kmol NH3 /s = 179.74 mol N/s
= 2.516 kg N/s = 219.608 tonnes N/day
From 2., we get, Area required, A = 21.961 m2
Hence, Diameter = 5.288 m
From 3., we get, Pt required = 70.275 kg
From 1., we get, Pt/gauze = 8.784 kg
Hence, we get, Number of Gauzes = 70.275/8.784 = 8 gauzes
Platinum and Rhodium prices were acquired from [14] and [15] respectively. Since the
catalyst life is 6 months, we are using 2 batches of catalyst gauzes per year. We are also
capitalising 24 months worth of catalyst.
The burner head is vertical, conical vessel with the following specifications:
According to the Internal Pressure Vessel calculations, to find the regulation thickness,
t, referring to CL 407 Handouts [16],
P Di
t=
2 cos α[Sa E − 0.6P ]
Hence we get, t = 11.7 mm. Now to get the trec , we have,
t+c
trec = m = 14mm
1 − 100
Hence, weight of the Burner head = 6,336.2 lbs
From Walas et. al. [11], we have Vertical Pressure Vessels cost, C as (The formula
provides values for 1984 in US$ with CE Cost Index = 315),
C = FM Cb + Ca
Cb = 1.672exp[9.1 + 0.2889(lnW ) + 0.04576(lnW )2 ]
Ca = 480D0.7396 L0.7066
where W - shell weight in lbs, D - Diameter in ft and L - Height in ft. On using the
required values we get the following results:
D L FM Cost Cost
W (lbs) Cb Ca Cost (INR)
(ft) (ft) (SS 321) ($, in 1984) ($, in 2018)
6,336.20 6.6 8.7 23805.9 4562.2 1.87 49,079.10 105,883.20 72.36 Lakhs
We produce 62% Nitric Acid solution at 1500 tonnes/day, which corresponds to 45.2
m3 /h. Referring to Walas et. al. [11] we will require a Field Erected Storage Tank
of height 20 m and diameter 33 m with a capacity of 4.5 million gallons, keeping an
inventory of 15 days of Nitric Acid. Nitric Acid Solution is stored under ambient atmo-
spheric conditions. We also require an Ammonia Storage Tank to store our Ammonia
for a period of one month to account for imports and procurement of the raw material.
Ammonia is stored at -33◦ C and 1 atm abs. For this, special Double walled Tanks are
constructed on site with a refrigeration unit accompanying the same. Ammonia required
is 267 tonnes/day, which corresponds to 16.5 m3 /h. All the calculations include pumps
installed in the tank farm as a factor of the total equipment cost [13]. Referring to
Fertilizers Manual [17], we will require a LT Carbon Steel Refrigerated Double Walled
Storage Tank, of height 20 m and diameter 28 m with a capacity of 3.25 million gallons.
Suggestions for inventory were given by Krupp Uhde [13]. Referring Fertilizers Manual
[17], Refrigerated Double Walled Ammonia Storage Tank incurred a capital cost of $
3.22 million in 1992-1994. Using CE Cost Index of 360 for the said period, multiplying
CE Cost Index of 2018, 603.1, and multiplying $ to INR conversion factor of 70 and 1.1
we get,
Refrigerated Ammonia Storage Cost = INR 41.52 Crores
The following relation is used for costing of Field Erected Storage Tanks (C calculated
in $, all values for 1984 with CE Cost Index = 315):
Temp.
Storage Dim. Volume C C
And MoC FM Cost (INR)
Tank (m) (gal) ($, 1984) ($, 2018)
Pressure
Nitric Acid D = 33 T = 30◦ C 4.52
SS 304L 2.4 1,019,978.60 1,952,854.30 15.04 Crores
Storage H = 20 P = 1 atm million
Hence, the total cost required for Storage Tanks = INR 56.56 Crores
Equipment Sizing and Costing 49
9.3 Compressors
There are two compressors in the plant - C101 to compress the Air feed from ambient
conditions to 5 bar abs before the Ammonia Oxidation Reactor and C102 to compress
the oxidised NOX gases to a pressure of 12 bar, for the high pressure absorption column.
Both the compressors are Two Stage Centrifugal Compressors with turbines, with the
Air Compressor, C101 having a compression ratio of 2.236 and the NOX Compressor,
C102 having a compression ratio of 1.549. The choice to use a multi-stage compressor
was made because the temperature increase due to compression in one single stage
could have damaged the compressor in both the cases and also due to the fact that the
power requirements and the flow rates were in the range of the operating conditions for
centrifugal compressors. [13]
Calculations are shown for the first stage of the C101, Air Compressor, with Air coming
at 189.06 tonnes/hour.
Similar calculations for other stages and compressors yield the following results:
For cost estimation, Nomograms from Peters et. al. [10] are used. Referring the nomo-
grams, we get the following results for the compressor cost estimation:
** Note that both the compressors are Two Stage Centrifugal Compressors
with Turbines
Equip. Power
Pin - Pout Process Cost Cost
No. - Required MoC Cost INR
(bar abs) Fluid ($, 2002) ($, 2018)
Stage (kW)
P1 = 1 36.88
C101 - 1 Air 5237.5 CS 3.1 million 4.789 million
P2 = 2.236 Crores
P1 = 2.236 49.96
C101 - 2 Air 7042.9 CS 4.2 million 6.488 million
P2 = 5 Crores
P1 = 5 16.65
C102 - 1 NOX Gas 2037.2 SS 304L 1.4 million 2.163 million
P2 = 7.745 Crores
P1 = 7.745 19.04
C102 - 2 NOX Gas 2350.1 SS 304L 1.6 million 2.472 million
P2 = 12 Crores
9.4 Pumps
There are a total of 6 estimated pumps in the plant. Including standby pumps, we have
a total of 12 pumps. Out of these 12, 6 are part of the cooling circuit of absorption
column and their cost is incorporated into the costing of the absorption column using
the data provided by Krupp Uhde [13]. Out of the remaining pumps, one set is used to
pump liquid ammonia into the plant, one set is used to pump the acid condensate to the
absorption column and the last set is used to pump the required water into the boiler for
production of steam. Sample calculation for the liquid Ammonia pump is shown below.
Liquid Ammonia is fed at 19 bar to the Ammonia evaporator from the Ammonia Storage,
which stores ammonia at 1 bar and -33◦ C. Since the temperature is so low, LT Carbon
Steel is used as the MoC of this pump.
Flow rate = 3.056 kg/s; Pressure difference = 18 bar; Density of liquid = 610 kg/m3
∆P ∆Pf
WP = + g∆z +
ρ ρ
All pumps used here fall under the zone of Centrifugal Pump considering the flowrate
and the head required. The following relations from Walas et. al. [11] are used to
estimate individual pump costs, C (Calculated values in $ for 1984, with CE Cost Index
= 315):
C = FM FT Cb , base cast − iron, 3550 rpm, V SC
√ √
Cb = 3exp[8.833 + 0.6019(lnQ H) + 0.0519(lnQ H)2 ]
√ √
FT = exp[b1 + b2 (lnQ H) + b3 (lnQ H)2 ]
Type b1 b2 b3
One-stage, 1750 rpm, VSC 5.1029 -1.2217 0.0771
One-stage, 3550 rpm, HSC 0.0632 0.2744 -0.0253
One-stage, 1750 rpm, HSC 2.029 -0.2371 0.0102
Two-stage, 3550 rpm, HSC 13.7321 -2.8304 0.1542
Multistage, 3550 rpm, HSC 9.8849 -1.6164 0.0834
Based on the tables and cost relations provided above, we get the following results for
the pump cost estimations:
Equipment Sizing and Costing 52
** Note - All the above mentioned Pumps are Centrifugal pumps. Cost
include the costing of both A/B pumps for each set
Flow
Process Head Type - Cost Cost
Pump rate Cost INR
Fluid (ft) MoC ($, 1984) ($, 2018)
(gpm)
Two-Stage,
P101 Liquid
79.5 1001.2 3550 rpm, 17,233.40 32,995.10 25.41 Lakhs
(A/B) Ammonia
HSC - CS
One-Stage,
P102 Nitric
127.7 250.1 3550 rpm, 17,495.30 33,496.50 25.80 Lakhs
(A/B) Acid
HSC - SS 304L
Boiler One-Stage,
P103
Feed 52.6 322.5 3550 rpm, 7,721.50 14,783.60 11.39 Lakhs
(A/B)
Water VSC - CS
Hence, the total cost required for Pumps = INR 62.60 Lakhs
There are a total of 8 Heat Exchangers in the plant. All the heat exchangers are Shell
and Tube Heat Exchangers, as cross checked with Krupp Uhde [13] and DFPCL [7].
The waste heat boiler is sized below.
TLMTD = 405.4◦ C
Overall Heat Transfer Coefficient for Gas-Water Heat Exchange, U = 150 W/(m2 .K)
A = Q / (U * TLMTD ) = 428.62 m2
Equipment Sizing and Costing 53
The cost estimate for heat exchangers is performed using the nomograms available in
Peters et. al. [10], where the cost from nomogram was in $ for 2002, with CE Cost
Index = 390.4:
HE101- HE101-
HX No. WHB HE102 HE103 HE104 HE105 HE106
AE AS
Cooling
Hot Stream LP Steam NO Gas NO Gas NO Gas NO Gas NO Gas Air
Water
Thot, in (K) 306 423 1123 700 568 457 530 493
Thot, out (K) 280 372 700 568 457 323 323 323
Cold BFW/ Cooling Cooling
Ammonia Ammonia Tail Gas BFW Tail Gas
Stream Steam Water Water
Tcold, in (K) 240 283 353 403 313 306 306 283
Tcold, out (K) 283 343 653 623 353 330 330 403
Q (kW) 4472 412.7 26063.9 8667.8 7282.3 13883.7 5765.7 4675.1
U (W/m2 .K) 150 300 150 95 150 150 150 95
Area (m2 ) 970.5 16.3 428.7 790.2 274.1 1692.1 517.8 798.2
Shell Side
Ammonia LP Steam NO Gas Tail Gas BFW NO Gas NO Gas Air
Fluid
Shell Side SS 304L SS 304L
LT CS CS SS 321 SS 321 SS 304L SS 304L
MoC 2Re10 2Re10
Tube Side Cooling BFW/ Cooling Cooling
Ammonia NO Gas NO Gas Tail Gas
Fluid Water Steam Water Water
Tube Side SA 192/ SS 304L SS 304L
LT CS SS 321 SS 304L SS 304L SS 304L
MoC SA 213 2Re10 2Re10
Pressure Tube:12
6.5 5 5 5 5 5 12
(bar abs) Shell:5
Cost
54,150 5,054 197,534 191,301 60,078 704,968 346,418 177,650
($ , 2002)
Cost
83.7 7.8 305.2 295.5 92.8 1,089.10 535.2 274.4
(1000$, 2018)
0.65 0.061 2.35 2.28 0.72 8.39 4.12 2.11
Cost INR
Crores Crores Crores Crores Crores Crores Crores Crores
Hence, the total cost required for Heat Exchangers = INR 20.67 Crores
9.6 Columns
We have two Absorption Columns in our plant, one is a 47 m tall reactive absorption
column and the second one is a 10 m tall bleaching column. Since the absorption column
has a height greater than 10 m, we need to make thickness calculation based on stresses
produced due to wind at heights. We can ignore this for the shorter bleaching column.
We use internal pressure vessel and wind force calculations to find out the thickness
required for the column body and heads.
Using Internal Pressure Vessel calculations, referring to CL 407 Handouts [16], we have,
P Di
t=
2[Sa E − 0.6P ]
Both the columns have ellipsoidal heads, using details from CL 407 Handouts [16],
similar calculations are done for the heads and the skirt. The details of the calculations
are provided in the detailed design of the absorption column. Following the thickness
calculations, weights of the columns were calculated, skirts and heads included.
** Note - The bottom closure of the absorption column, A101 has a separate
vessel attached inside, with its weight being 0.25 times that of the closure
itself, according to the data provided by Krupp Uhde [13].
[13], once the entire column cost is calculated, including trays, multiplying a
factor of 1.25 will give a rough estimate for the entire column cost including
the cost of the cooling system.
Nomograms from Peters et. al. [10] are used, where the cost from nomogram was in $
for 2002, with CE Cost Index = 390.4:
A101 - B102 -
Column
Absorption Column Bleaching Column
Height (m) 44.6 9
Diameter (m) 4 1.75
Tray Spacing 1 m / 1.2 m 0.6 m
trec for Body (mm) 18.3 4.55
trec for Heads (mm) 18.24 4.54
trec for Skirt (mm) 3.77 3.77
Skirt Height (m) 3.4 1
NO-NOx Gases, Air, NOx Gases,
Fluids Processed
Nitric Acid Nitric Acid
Operating Pressure
11 4
(barg)
Operating Temp.
10 - 50 30 - 50
Range (◦ C)
Design Pressure
12.1 4.4
(barg)
Design Temp.
80 80
(◦ C)
MoC SS 304L SS 304L
Weight (Tonnes) 88.46 2.006
Cost ($, 2002) 700,000 52,000
Cost ($, 2018) 1,081,378 80,331
Cost INR 8.33 Crores 0.62 Crores
Sieve trays are used in both the absorption columns due to their many benefits. Selection
process, the tray specification and calculations for number of trays for absorption column
are all specified in the detailed design of the absorption column.
Nomograms from Peters et. al. [10] are used for cost estimation, where the cost from
nomogram was in $ for 2002, with CE Cost Index = 390.4:
Hence, the total cost required for Columns, including the cooling system = INR 13.43
Crores
Chapter 10
Plant Economics
This chapter focuses on an overview of the plant economics, by estimating the capital
investments, production costs and finally the payback period for the Nitric Acid Plant.
The Dual Pressure Nitric Acid plant has many major equipments including storage
tanks, compressors, pumps, heat exchangers, reactor and columns. We used costing
relations provided by Peters et. al. [10] and Walas et. al. [11] to determine the total
purchased cost of each of these equipments, using CE Cost index to find their costs in
2018. A dollar to INR factor of 70 is used and an India location factor of 0.7 is also
used. The following is the final result of our calculations in Chapter 9:
57
Plant Economics 58
Total purchased equipment costs calculated in the prvious section are used to calculate
the total capital investment in the plant. Working capital is calculated as 15% of the
total capital investment. The plant is considered to be a Fluid-Fluid Processing plant
(F-FPP) and the percentage of delivered equipment cost is implemented for this cost
estimation. The results of the estimation are provided in the table below:
Indirect Costs
Engineering and Supervision 33 0.0655 71.12
Construction Expenses 41 0.0813 88.36
Legal Expenses 4 0.0079 8.62
Contractor’s Fee 22 0.0437 47.41
Contingency 44 0.0873 94.82
Total indirect plant cost 144 0.2857 310.33
Peters et. al. [10] is used as the reference for this costing exercise, using the ratio factors
provided by it for our cost estimation.
The estimation of the total product cost comes from raw material cost. We require
Liquid Ammonia as a raw material, which is acquired via imports and from KRIBHCO,
and we also require 140.55 kg of Pt-Rh catalyst gauzes every year, taken from Johnson
Matthey India Pvt. Ltd. Ammonia cost is acquired from data provided by DFPCL [7].
Raw material cost calculation is provided below:
The plant revenue is calculated from the untaxed prices of 62% Weak Nitric Acid (WNA)
Solution, sold at INR 20/kg, with 1$ = INR 70, cost taken from data provided by DFPCL
[7]. The results are tabulated below:
Total Product cost is calculated using the normalised percentage method from Peters
et. al. [10].The result is reproduced in the following tabulated form:
The following assumptions were made while making the payback period calculations:
• 90% of FCI excluding the land costs is considered to be depreciable over a period
of 10 years.
• Final Product and Raw Material costs are assumed to be constant for profit cal-
culations.
Using 70% production capacity for year 1, 80% for year 2, 90% for year 3 and 100%
thereafter, the following cash flow diagram was generated,
Table 10.6: Cash Flow from Plant production, all values in INR Crores
Plant Economics 62
The usual payback period for a nitric acid plant is anywhere between 4-6 years [13].
The following comparison with economics of a 500 TPD Dual Pressure Plant set up in
Donaldsonville, Louisiana, United States by Uhde in collaboration with CF Industries in
2016, shows that our plant economics are in accordance with actual industry economics.
The dual pressure process, requires an absorption column to absorb NOX gases from
the gaseous reactor into water and produce the desired concentration of nitric acid. The
column handles three streams - (1) gas stream at 1,76,573 kg/hr, containing 13.35% by
weight of nitrogen oxides at 50◦ C and 12 bar abs, (2) deionised make up water at 11,987
kg/hr, 10◦ C and 12 bar abs and (3) 37.8% nitric acid condensate from cooler condensers,
at 25770 kg/hr, 50◦ C and 12 bar abs. The column is required to produce 62,673 kg/hr
of 62% HNO3 solution, excluding the dissolved NOX gases.
A rigorous mathematical model was also produced for this column, to determine the
exact number of trays for the entire column, using correlations and data from Ray et.
al. [8] and Thiemann et. al. [6]. The model was run using MATLAB and Google
Spreadsheets.
63
Detailed Design - Absorption Column 64
A rigorous mathematical model was used in sizing the column and determining the exact
number of trays required for our column. The model is summarised below:
• Tray by tray approach based on the given feed compositions, temperatures and
pressure is implemented
• First, NO oxidation conversion is calculated using correlations from Ray et. al. [8]
and gas composition is recalculated - Step 1
• Next, the amount of nitric acid formed in each plate is calculated using tray effi-
ciency and related terms, available in Ray et. al. [8] and derived from Thiemann
et. al. [6], and both liquid and gas phase compositions are recalculated - Step 3
• Method is repeated until a tray achieves an almost zero concentration nitric acid.
Tail Gas composition and the required amount of make up water are calculated at
the end. Energy balances are also performed during each iteration.
The model was solved using an iterative method, implemented by solving 3 functions
iteratively on MATLAB R2015b, using the fsolve function. Solutions from MATLAB
were iteratively fed to Google Spreadsheets for the gas composition recalculation, as
MATLAB R2015b didnt allow for the functions to defined within its for loops. The
code can be found in the Appendix B.
2N O + O2 → 2N O2 , ∆H = −112.7kJ/mol
2N O2
N2 O4 , ∆H = −58.1kJ/mol
3
N2 O4 + H2 O
2HN O3 + N O, ∆H = −75.0kJ/mol
2
The results of the mathematical model are tabulated below:
Detailed Design - Absorption Column 65
Temp. for section below Tray 13 - 50◦ C - Cooled using cooling water
Temp. for section above Tray 13 - 10◦ C - Cooled using chilled water
Step 1 -
X - NO conversion
k1 - NO Oxidation reaction rate constant
t - Residence time of gas between trays
P - Operating Pressure
b - Mole fraction of oxygen in gas
2a - Mole fraction of NO in gas
Step 2 -
Step 3 -
The following parameters were considered while selecting the type of tray for the column:
Sieve Trays were finally selected because of their versatile properties, making them
feasible for almost every condition.
Plate Design Procedure provided in Sinnott et. al. [18] is used for our design. Sieve
Trays of the following specifications are used in the absorption column:
Column Diameter, Dc = 4m
Area, Ac = 12.57 m2
Downcomer Area, Ad = 0.12 Ac = 1.51 m2
Net Area, An = Ac - Ad = 11.06 m2
Active Area, Aa = Ac - 2Ad = 9.55 m2
Hole Area, Ah = 0.1Aa = 0.955 m2
Referring to Sinnott et. al. [18], we get lw /Dc = 0.77 for given hole area, hence
Weir Length, lw = 0.77Dc = 3.08 m
Weir height = 50 mm
Detailed Design - Absorption Column 68
Referring to Sinnott et. al. [18], we get K2 = 30.2 for given hw + how , hence
Uh,min = (30.5 - 0.9(25.4 - 5))/(13.27)0.5 = 3.25 m/s
Actual minimum vapour velocity = 3.333 m/s
So, the minimum operating rate will be above the weep point.
So, total plate pressure drop, ht = 10.84 + 9.43 + 50 + 20.05 = 90.32 mm liquid =
1.174 kPa
Referring to Sinnott et. al. [18], we get θc = 102◦ for given hole area and plate thickness,
hence,
Angle subtended at plate edge by unperforated strip = 180 - 102 = 78◦
Detailed Design - Absorption Column 69
Figure 11.2: Sieve Tray Cooling Coils, Image provided by Krupp Uhde [13]
The column is an internal pressure vessel, with cylindrical body and ellipsoidal heads.
Cylindrical Body -
P Di
t=
2[Sa E − 0.6P ]
Ellipsoidal Heads -
P Di
t=
2[Sa E − 0.1P ]
Insulation diameter = 5 m
Area = 240 m2
Wind velocity = 70.4 mph1
Pw = 0.002*70.42 = 9.905 psf = 474.25 Pa
Force = Pw * G * Area = 474.25 * 1.9 * 240 = 216.3 kN
A Detailed Mechanical Drawing of the Absorption Column, with all design specifications
is available in Appendix C
1
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LEVEL=162&MOD=tab
Chapter 12
Environmental Impact
Only one waste stream exits our plant - Tail Gas containing pollutants NO and NO2 ,
widely known to be precursors to acid rain and smog, and greenhouse gas N2 O, having
a global warming potential 280 times that of CO2 . Though there is no statutory limit
on N2 O emissions in India, United Nation’s Clean Development Mechanism provides
monetary benefits for reducing N2 O emissions. NOX have a strict limit to be followed
for Nitric Acid Plants in India, and we require an abatement unit to take care of reducing
these emissions.
The table below shows the composition of the Tail Gas leaving the Absorption Column:
73
Environmental Impact 74
According to the data from the Ministry of Environment, Forest and Climate Change of
the Central Government of India [19], the permissible emission levels of NOX for Nitric
Acid Plants is 400 mg/m3 or 400ppmv. Since our NOX emissions are over the limit, we
will require an abatement unit to reduce the NOX levels.
EnviNOX
R
by Uhde GmbH is world’s best abatement technology for Nitric Acid Plants.
The EnviNOX
R
Unit provides >97% NOX and >98% N2 O removal, ensuring minimal
pressure drop (<40 mbar), for an average period of more than 10 years.
Referring Groves et. al. [20], many process variants of this technology are available, but
we will be using the EnviNOX
R
process variant-2 for our nitric acid plant. The rea-
sons for choosing this is the lower reducing agent costs and lower reaction temperature
requirements for achieving very high emission reductions. Catalysts used in this tech-
nology, EnviCat
R
-NOX and EnviCat
R
-N2 O, are both Iron Zeolites, used individually
in the DeNOX and DeN2 O
R
stages.
Being a propreitary technology, Uhde has given exclusive rights to Clariant and Süd
Chemie for production of these catalysts for the vast nitric acid process market.
EnviNOX
R
process variant-2 involves preheating the tail gas using the secondary air and
the reactor outlet gas stream to a temperature of 350◦ C at 12 bar abs. Stoichiometric
amounts of gaseous ammonia are mixed with the tail gas before entering the reactor
unit containing the catalyst pellets in an annular porous cylindrical setup. Ammonia
reduces NOX in the DeNOX stage of the reactor unit, ensuring that the DeN2 O
R
process
downstream doesn’t get hampered by the presence of NOX in the tail gas. Propane is
added to this mixture, which acts as a reducing agent for N2 O in the DeN2 O
R
stage,
removing >98% N2 O from the tail gas, giving us vastly reduced emissions for our plant.
The tail gas can is then expanded in the tail gas turbine. The tail gas turbine provides
around 65% of the power required to run the compressors.
DeNOX Reactions:
6N O2 + 8N H3 → 7N2 + 12H2 O
4N O + 4N H3 + O2 → 4N2 + 6H2 O
Environmental Impact 75
DeN2 O
R
Reactions:
10N2 O + C3 H8 → 10N2 + 3CO2 + 4H2 O
A catalyst volume of 7m3 is used, as suggested Krupp Uhde [13]. This volume of catalyst
gives us a N2 O removal of 98.5% and NOX removal of 97%. The final tail gas composition
is shown in the table below:
The reactor is an annular cylindrical fixed bed reactor, with two catalyst bed of around
3.5 m3 each, filled inside a perforated cylinder, to allow gas flow from outside the cylinder
to the inner annular region. The beds are housed inside a cylindrical shell of 5 m internal
diameter, with ellipsoidal heads, operating at 12 bar abs. The MoC used is SS 321.
According to the data provided by Krupp Uhde [13], the reactor setup is designed by
Uhde GmbH and will cost around INR 1 Crore for the given catalyst volume. Hence,
Additional Ammonia costs were included in the Raw Material Cost Estimation done in
Chapter 10
Total Propane costs per year = INR 32,03,690 / year = $ 45,767 / year
Using the method outlined in Chapter 10, calculation were again done, giving us,
Environmental Impact 77
Since the prices of CERs fluctuate from year to year, two calculations were done for
calculating the payback period, (1) without the CER Revenue, and (2) with the CER
Revenue.
According to the UN’s Clean Development Mechanism, project registered under it will
be rewarded with 1 CER / tonne CO2 eq. reduced below the baseline for the entirety of
the crediting period. The baseline model was selected to be the emission from the plant,
as India doesn’t have any limits on N2 O emissions. The baseline model was selected
after referring to Methodology AM0028 [21], accessible from the CDM portal of UN.
Emission Reduction = (142 - 2.13)*8000 = 1119 tonnes N2 O = 3,12,973 tonnes CO2 eq.
Hence, the revenue earned from CER trading, will help us recover the fixed capital
investment required for setting up the abatement unit.
3
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Appendix A
The Final Process Flow Diagram with the Stream Table is shown below. The collective
image was taken using Google Spreadsheets. The PFD was made using draw.io.
79
Line No 1 1C 1D 2 2A 3 4 5 6 7 8 8A 9 10 11 12 13 14 15 16 17 18 19
Stream Comp. Air feed Primary Air Secondary Air Ammonia Feed Evaporated NH3 Reactor Inlet Reactor Outlet HE102 Outlet HE103 Outlet Acid Condensate NOx Comp. inlet NOx Comp. Outlet Absorption Inlet Tail Gas Absorption Outlet Process Water Bleaching Air Nitric Acid Pdt Mixed Tail Gas Reduced Tail Gas Tail Gas Out Reducing Ammonia Propane
Phase g g g l g g g g g l g g g g l l g l g g g g g
NH3 0.00 0.00 0.00 11003.30 10963.30 10963.30 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 40.00 0.00 0.00 40.48 0.00
O2 43518.85 39004.55 4514.30 0.00 0.00 39004.55 13569.84 12125.47 9855.66 0.00 8590.66 8590.66 7042.89 3306.59 0.00 0.00 4514.30 0.00 3306.59 3291.59 3291.59 0.00 0.00
N2 145541.03 128386.69 17154.34 0.00 0.00 128386.69 128657.55 128657.84 128657.84 0.00 145812.18 145812.18 145812.18 145812.18 0.00 0.00 17154.34 0.00 145812.18 145966.09 145966.09 0.00 0.00
H2O 0.00 0.00 0.00 0.00 0.00 0.00 17412.30 17412.30 17412.30 16019.32 0.00 0.00 0.00 0.00 23815.84 11986.72 0.00 23815.84 0.00 87.18 87.18 0.00 0.00
N2O 0.00 0.00 0.00 0.00 0.00 0.00 141.88 141.88 141.88 0.00 141.88 141.88 141.88 141.88 0.00 0.00 0.00 0.00 141.88 2.13 2.13 0.00 0.00
NO2 0.00 0.00 0.00 0.00 0.00 0.00 0.00 4153.16 10679.54 0.00 18932.46 18932.46 23382.28 17.75 2319.83 0.00 2319.83 0.00 17.75 0.54 0.54 0.00 0.00
NO 0.00 0.00 0.00 0.00 0.00 0.00 18573.12 15864.54 11608.20 0.00 3095.52 3095.52 193.47 58.05 0.00 0.00 0.00 0.00 58.05 1.74 1.74 0.00 0.00
HNO3 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 9750.89 0.00 0.00 0.00 0.00 38857.50 0.00 0.00 38857.50 0.00 0.00 0.00 0.00 0.00
CO2 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 41.96 41.96 0.00 0.00
C3H8 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 0.00 15.00
Total 189059.88 167391.24 21668.64 11003.30 10963.30 178354.54 178354.69 178355.18 178355.42 25770.20 176572.69 176572.69 176572.69 149336.44 64993.17 11986.72 23988.47 62673.34 149376.44 149391.23 149391.23 40.48 15.00
Pressure (bar) 1.00 5.00 5.00 1.00 5.00 5.00 5.00 5.00 5.00 12.00 5.00 12.00 12.00 12.00 12.00 12.00 5.00 5.00 12.00 12.00 1.00 12.00 12.00
Temperature (C) 35.00 240.00 240.00 -33.00 70.00 230.00 427.00 300.00 185.00 50.00 50.00 260.00 50.00 130.00 50.00 10.00 80.00 50.00 350.00 350.00 35.00 350.00 350.00
Appendix B
AbsorptionColumn.m File
1 clear all ;
2 clc ;
3 X1 = fsolve ( @myfunc , 0.5) ;
4 Gno2 = fsolve ( @myfunc3 , 0.5) *1 . 4 8 7 3 9 1 84 1 / 1 2 ;
5 F = fsolve ( @myfunc2 , 0.5) ;
6 % Gno2 = fsolve ( @myfunc3 , 0.5) * 1 . 5 8 7 7 0 2 8 8 8 / 1 2 ;
7 % [ p1 , p2 , p3 ] = myfunc4 () ;
8 % p = [ p1 , p2 , p3 ];
9 % roots ( p ) * 1 . 5 5 2 5 7 3 2 0 2 / 1 2
Solving Step - 1
1 function [ y ] = myfunc ( x )
2
3 Vw = 1765 76.4/360 0;
4 G = 1.614361111;
5 b = 0 .061583 33333/ G ; % O2 molfrac
6 a = 0 . 0 0 1 8 0 5 5 5 5 5 5 6 / ( 2 * G ) ; % NO molfrac
7
8 T = 283;
9 P = 12;
10 rhov = P *100*( Vw / G ) /(8.314* T ) ;
11 k1 = (10^((635/ T ) - 1.0261) ) /(8.206* T *10^ -3) ;
81
Environmental Impact 82
Solving Step - 3
1 function [ y ] = myfunc2 ( f )
2
3 X = 0.7804;
4 P = 12;
5 T = 307.68;
6
7 V = 152108.312/3600;
8 Gno = 0 . 0 0 0 0 1 4 1 8 7 0 0 9 6 8 ;
9 Gno2 = 0.0041;
10 Gn2o4 = 0 . 00 65 10 5 81 49 5;
11 Gnox = Gno2 + Gn2o4 ;
12 G = 1.487318477;
13 Ghno3 = 0.000 2849531 8;
14 Gh2o = 0.1785554731;
15
16 Pno = P * Gno / G ;
17 Pno2 = P * Gno2 / G ;
18 Pn2o4 = P * Gn2o4 / G ;
19 Pnox = Pno2 + Pn2o4 ;
20
21 A = 10^(8.756 - (2838/ T ) ) ;
22 B = ( T /210.3) + (790/ T ) - (3.8794) ;
23 k2 = A *(1 - B * Pnox ) ;
24 w = ( Ghno3 *63) /( Ghno3 *63 + Gh2o *18) ;
25 rhol = ( Ghno3 *63 + Gh2o *18) /(( Ghno3 *63/1513) + ( Gh2o *18/1000) ) ;
26 nHNO3 = ( Ghno3 *63) /(( Ghno3 *63 + Gh2o *18) *10/ rhol ) ;
27 k4 = 10^(7.412 - 20.28921* w + 32.47322* w * w - 30.87* w * w * w ) ;
28 k3 = k4 / k2 ;
29 function [ f ] = myfunc5 ( x )
30 f = 3* k3 * x * x * x + (2* x * x / k2 ) + x - 3* Pno - Pnox ;
31 end
32 E = fsolve ( @myfunc5 , 0.5) ;
33 rhov = P *100*( V / G ) /(8.314* T ) ;
34 H = 0.04;
35 nNONOx = ( Gno *30 + Gno2 *46 + Gn2o4 *92) /(10* V /( rhov ) ) ;
36 R = ( Pno + Pnox ) / P ;
37 if R < 0.01
Environmental Impact 83
The detailed drawing for the Absorption Column was made using Adobe Illustrator.
The detailed calculations to arrive at the dimensions have been shown in Chapter 11.
84
4m
Tail Gas to HE106 Tail Gas to HE106
N105
1.56 m
Demister
Material of Construction
1.5 m
Cooling Coils N104
Process Water Inlet
For the column : SS304L (Nitric Acid Grade)
N069/N070
For the skirt : CS
PLATE 35
1.2 m Manhole 7
N067/N068
PLATE 34
Operating Parameters
N065/N066
PLATE 33
Operating Pressure - 11 barg
N063/N064 Operating Temperature - 283-323 K
PLATE 32 Weak Acid Feed (Plate 12) - 25770 kg/hr
N061/N062
Process Water Feed (Plate 35) - 11580 kg/hr
PLATE 31 NO Gas feed (Column Bottom) - 176577 kg/hr
N059/N060
PLATE 30
N049/N050
PLATE 25
N047/N048
Nozzle Details
PLATE 24
Cooling Coils
N045/N046
PLATE 23
1) N001-N024, N071-N072 - Cooling Water Cooled coils
- Diameter : 2-4 inches
Manhole 5
N043/N044 2) N025-N070 - Chilled Water Cooled coils
PLATE 22 - Diameter : 2 inches
N041/N042
PLATE 18
- Diameter : 4 inches
N033/N034 7) N105 - Tail Gas Outlet
PLATE 17
- Diameter : 8 inches
Manhole 4
N031/N032
PLATE 16 Manholes
8) Manhole 1-Manhole 7 - Diameter: 0.6 m
N029/N030
PLATE 15
N027/N028
PLATE 14
N025/N026
Design Notes
PLATE 13
N103
1.2 m Weak Acid Inlet 1) Distance between the plates : Plate 0 to Plate 12 - 1 m
PLATE 12
N023/N024
Plate 12 to Plate 35 - 1.2 m
1m 2) Fillet weld joining column cylinder to ellipsoidal heads
N021/N022
PLATE 11
3) Stainless Steel plate is used to join the skirt and the column
Manhole 3
4) Exact representation of manhole and pipe positions is as in figure 2
PLATE 10
N019/N020
5) For figure 1, cooling coils are not diametrically opposite for consecutive
trays, they are represented as such for ease of viewing.
N017/N018
PLATE 9
N015/N016
PLATE 8
N013/N014
PLATE 7
N011/N012
PLATE 6
N009/N010
PLATE 5
Manhole 2
N007/N008
PLATE 4
N005/N006
PLATE 3
N003/N004
PLATE 2
N001/N002
PLATE 1
1m
N071/N072
PLATE 0
1.5 m NOX
N101 Gas
NOX Gas Inlet Inlet
0.44 m
1.56 m
Process Water Inlet
4.5 m
Weak Acid Inlet
N102
Product Acid Outlet
Product Acid Outlet Cooling/Chilled Water Inlet
1.8 m
0.6 m
Manhole 1
Appendix D
DWSIM Flowsheet
The Process Flowsheet was developed using DWSIM simulations software. It is an Free
and Open Source software. More info on DWSIM can be found here
86
References
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