Theoretical Calculations on Simultaneous Emission Removal from a
Waste Gasification Plant
ILIRJAN MALOLLARI, TERKIDA VASO, GRESADA ÇOÇKA
Chemical Process Engineering Group, Department of Industrial Chemistry,
Faculty of Natural Sciences,
University of Tirana, Boulevard ZOGU I , 25/1, Tirana1057
ALBANIA
Abstract:- This study presents a detailed and comprehensive methodology for theoretical engineering
calculations in a modelled waste gasification plant. The aim is to determine the most effective way to clean
up exhaust gases or emissions from industrial combustion processes. The pollution from chemical processes
is significant due to the direct emission of harmful gases into the atmosphere, such as SOx, NOx, COx, O3,
etc. To achieve this, we utilised the ASPEN PLUS simulation computer program, which facilitated a series
of theoretical calculations during the procedure and optimisation of capturing the abovementioned
dangerous gases and cleaning them out. This work involves two processes: the absorption of chimney's
emissions from waste gasification plants, which consists mainly of a reactor and an absorber, and cleaning
the contaminated remaining liquid from the absorber at the end of the capturing process. Through
meticulous simulation and computer calculations, we have determined the absorbing rate of the polluting
gases and completed a thorough sensitivity analysis for the entire process. This precision in our calculations
instils confidence in our results' reliability and the proposed methods' potential effectiveness, reaffirming
the trust in our research findings.
Key-Words: environmental pollution, pollutant gases, gas oxides, simulation, absorbing solutions, emission
reduction.
Received: April 8, 2023. Revised: October 19, 2024. Accepted: November 13, 2024. Published: December 12, 2024.
1. Introduction
1.1. The process of capturing acidic oxides
consists of a reaction that makes oxidation
possible, followed by a cooler that cools the
oxidised gases. This mixer combines the NaOH
solution and an 'absorption column '. This column
is a critical component that allows the oxidised
gases to be absorbed, a crucial step in the
emission reduction process.
In the procedure below, the currents represent the
following: 1: the stream of ClO2 2: the stream of
polluting gases (NO, NO2, SO2, SO3, etc.); 3-
streams of oxidised gases 4- streams of cold water
5-flow of cold oxidised gases 6-flow of water and
NaOH; 7-stream leaving the mixer and containing
the cold NaOH solution; 8-the stream of steam
that is released from the absorber must contain as
few polluting gases as possible; 9-the solution
stream that leaves the reactor and includes all the
salts formed [1–3].
1.2. The process of the Acidic gases
Captured from the combustion processes
Through the process diagram flowsheet
preliminarily constructed by us (see Figs. 1 and
2), the capture of all the harmful gases that come
out of the chimneys of burning plants is realised
before releasing them into the atmosphere. In
stream 1, we have a mixture of gases where, in
addition to sulfur and nitrogen oxides, we also
have other 'polluting gases', a term used to
describe the gases that contribute to
environmental pollution [4–7].
The reactor used in this case is of the CSTR type,
a crucial component that enables the oxidation of
these gases by forming the corresponding salts of
each pollutant. In stream 2, we have ClO2, which
International Journal on Applied Physics and Engineering
DOI: 10.37394/232030.2024.3.9
Ilirjan Malollari, Terkida Vaso, Gresada Çoçka
E-ISSN: 2945-0489
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is used as an oxidiser. In-stream three, we have
oxidised gases, which pass to a scrubber or an
absorber, where water absorption becomes
possible [8–9].
Fig. 1:
Schematic presentation of the CSTR reactor
followed by an absorber in the simulation
software ASPEN PLUS.
Here, we have the separation of condensable
gases from non-condensable gases. Condensable
gases stay in the water and form 'polluting water',
a byproduct that requires further treatment. At the
fig. 2 it is presented a tentative process diagram
of acidic gases capture, where non-condensable
gases are released into the atmosphere because
they are harmless—the capture of combustion
gases. Through this scheme, we capture all the
gases that come out of the chimneys of plants or
factories as secondary material so as not to release
them directly into the atmosphere. Stream 1 has a
mixture of sulfur, nitrogen oxides, and other
polluting gases [11].
Fig. 2: Acidic gases capture process diagram
using EdrawMax software
In stream 2, we have ClO2, which is used as an
oxidiser. In stream 3, we have oxidised gases,
which then pass to a scrubber or an absorber
where absorption by water becomes possible [10].
Fig. 3 Schematic presentation of the CSTR
absorber in the simulation software ASPEN
PLUS.
Here, we have the separation of condensable
gases from non-condensable gases. Condensable
gases stay in water and form polluting water,
while non-condensable gases are released into the
atmosphere because they are harmless.
1.3.Capture of combustion gases.
Through this scheme, all the gases that come out
of the chimneys of plants or factories as
secondary material make it possible to capture
them so as not to release them directly into the
atmosphere. In stream 1, we have a mixture of
gases where, in addition to sulfur and nitrogen
oxides, we also have other polluting. The reactor
used in this case is of the CSTR type, which
makes it possible to oxidise these gases by
forming the corresponding salts of each pollutant.
In stream 2, we have ClO2 [12], which is used as
an oxidiser. In-stream three, we have oxidised
gases, which then pass to a scrubber or an
absorber where absorption by water becomes
possible. Here, we separate condensable gases
from non-condensable gases, which stay in water
and form polluting water. In contrast, non-
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DOI: 10.37394/232030.2024.3.9
Ilirjan Malollari, Terkida Vaso, Gresada Çoçka
E-ISSN: 2945-0489
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condensable gases are released into the
atmosphere because they are harmless [13-15].
2. Material and Methods
The general scheme worked on Aspen Plus is
formulated as in the flow sheeting of Fig 4.
Fig. 4: Full absorption process diagram of SOx
and NOx gases with solution ClO2 in ASPEN
PLUS V11.
The modelling and simulation of technological
processes were conducted using a standard
methodology. This approach, widely accepted in
the field, involves determining and optimising
process indicators and engineering capacities.
The physicochemical properties used in the
simulation were taken from the built-in databases
of the ASPEN PLUS software, ensuring the
results' accuracy and reliability.
For many scientific problems, especially
technological development, the data for the
dynamic construction of technological processes
does not exist. However, they are sufficient for
the so-called stationary (steady-state) models.
Because of this, the time dependencies of all
influencing parameters cannot be considered,
which is why the modelling and related
calculations become much more straightforward.
The simulation/modelling scheme represents
technological plants' construction, development,
and operation. Depending on the desired details,
we are dealing with fundamental technological
schemes, piping schemes, and instruments.
The simulation scheme graphically presents a
process, showing the basic operations for the
various parts of the plant, which are connected
through material and energy flows. By calculating
the mass and energy balances, it is possible to
calculate the mass and ratios of productive
currents, such as pressure and temperature.
Regarding the principle that through design and
modelling programs are carried out calculations,
we distinguish sequential modular calculations of
basic operations according to their arrangement in
the process diagram (flowsheet) and simultaneous
calculation of all stages through the passage of all
elements in the equalisation system.
Sequential modular calculation of individual
essential elements has some advantages in
modelling, as it performs comprehensible
simulations, detects errors, and offers the
possibility of adding models. Comparing it with
simultaneous calculations, we found some areas
for improvement in the case of opposite currents
and recycling between basic operations since they
have to be repeated many times. Let us consider
the flow control for the flowsheet simulation
performed throughout the computer program.
Through it, the models for calculating the
functions were obtained one after the other,
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basically mutually related to the data of subjects,
mixtures, or thermodynamic models. Other
numerical subroutines were used to solve linear
and non-linear equations encountered in separate
modules.
It is important to describe some of the essential
technological parts of operation by the chemical
reaction equations used while modelling various
technology processes for producing synthetic
fuels, together with their symbols.
3. Results and Discussion
Specifications for raw materials: In this work, the
raw materials are polluting gases and an oxidiser
that converts gases with a low oxidation number
into gases with the highest oxidation number. We
have raw NOx, SOx, CO2, O2, ClO2, and H2O
raw materials as in table 1.
Table 1 Some specific properties of the gases
Reactor feedstock: Gas flow: Polluting gases are
collected from all the chimneys of plants,
factories, or anywhere there is a combustion
reaction and the release of gases.
We have summarised the input data for the raw
material in the following table, which presents the
input current flows, the percentages of each
current component, the temperature of the input
components, and their pressure (see Table 2).
Values on this table has been taken from the
laboratory experimental characterisation for the
actual situation taken into account for this
research.
Table 2: Typical exhaust gas compositions
The input currents in this table are in ppm or %,
but in the Aspen Plus program, we have replaced
the unit kg/sec as the total flow as well as the
content of the components in the current. Rapid
Tables software was used for unit conversion,
which made it possible to convert ppm to
percentages, knowing the density of each
component and converting these percentages to
the program unit km/hr. First, we find the total
flow in km/hr and mp after each component (see
Table 3).
Table 3: Summary of component input measures
The input currents in this table are in ppm or %,
but in the Aspen Plus program, we have replaced
the unit kg/sec with the total flow and the content
of the components in the current.
Reactor specifications: The reactor used in the
process is of the CSTR type; its function is the
oxidation of gases. Some summary data for the
reactor
Components
(kg/m3)
Content
Density
(kg/m3)
NOx
200
ppm
1.34
SO2
65 ppm
2.93
O2
9 %
1.43
CO2
13 %
1.98
air
79%
1.29
Components
NOx, ppm
SO2’ppm
O2, %
CO2, %
Humid,ity %
Air
Waste-
burning
treatment
plant
200
65
9
13
0
78%
Conversion
in %
0,02
0,0065
9
13
0
78
Components
Kg/s
NO
9.5
SO2
6.06
O2
6.217
CO2
6.17
Air
72.056
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Fig. 5: Reactor completions in Aspen Plus V11
All reactions are kinetic and have their constants,
the release or acquisition of energy.
Fig. 6: Reactions entered in Aspen Plus V11
The feedstock of the reactor are the following
components: the stream of ClO2 and the stream of
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polluting gases (NO, NO2, SO2, SO3, etc.). A
packed tower is chosen as the absorbing device.
The packed towers are filled with packing
materials, such as ceramic Raschig rings.
Fig. 7. Total flowsheet process diagram
Tests in Aspen Plus: Our work in Aspen Plus has
been multiple, and each has an addition or
subtraction of the process. Evidence number 1: In
the program, I entered all the devices and all the
currents as shown in the theory above, but I could
not find a method that included NaOH; the
simulation went to the end, but the results were
not very satisfactory and expected.
The process calculation in the first trial consisted
of a CSTR reactor, a cooler, a mixer and an
absorber. The input streams in the process were
polluted gases, chlorine oxide, cold water in the
cooler, water needed to form the NaOH solution,
and the NaOH stream entering the mixer. The
completion seen in the figure above is done for all
other reactions.
The program entered all the devices and all the
currents, as shown in the theory above, but I
needed help finding a method that included
NaOH. The simulation went to the end, but the
results could have been more satisfactory. The
process in the first trial consisted of a CSTR
reactor, a cooler, a mixer and an absorber.
The input streams in the process were polluted
gases, chlorine oxide, cold water in the cooler,
water needed to form the NaOH solution, and the
NaOH stream entering the mixer. The completion
seen in the figure above is done for all other
reactions.
Fig. 8: Test number 1 in Aspen Plus
Test number 2
In test #2, We tried to dump the NaOH stream
from the mixer since it was not generated using
our method in Aspen Plus.
The process continued to generate results at the
end, but again, they did not obey our theory of
releasing as little gas as possible at the end. Again,
the process had the same equipment and initial
data in all currents and equipment specifications.
Fig. 9: Test number 2 in Aspen Plus
The following figure shows this process:
Test number 3
In test number 3, seeing that the mixer was not
playing an important role but only mixing water
with the temperature coming out of the cooler
with water coming from normal conditions and
seeing that their temperature was close to their
temperature in out of the mixer, we thought we'd
remove one and see what the results would be like
in the end.
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The simulation again ran to completion, and some
data was generated, but we still needed to meet
our expectations. The figure below shows the
process where the mixer is missing.
Fig. 10: Test number 3 in Aspen Plus
Test number 4
In this test, we added another device at the end of
the process where we have the solution output
containing the dissolved gas salts. Suppose these
crypts get out into the environment. In that case,
they can be harmful to the environment, and to
eliminate this occurrence, we have added another
absorption column where it is possible to absorb
these salts. The figure below represents this
simulation:
Test number 5:
Fig. 11: Test number 4 in Aspen Plus
In this test, it was added a second cooler and made
it possible to reduce the surface area of the cooler
by dividing it into two equal parts, that is, since in
the summary table of the supplement for the
cooler, we have an area of 1248 m2 by dividing it
into two equal parts for both exchangers is
624m2.
In Fig. 11, S1 represents the water entering the
cooler, S2 the exit of cold gas oxides, S3 the exit
of warm water from the first cooler (B1), S4 the
NaOH solution that enters the mixer (B2), S5 the
union of the three streams of water at the same
temperature, S6 water under normal conditions
enters the second cooler (B3), S7 warm water
from the second cooler, S8 cold oxides, S9 current
where we have the reduction of polluting gases,
S10 salt solution exit.
Test number 6: We have considered only SOx
reactions in this test, assuming these gases are
present only in the stream. The only difference is
that we have considered only the reactions that
occur for SOx, eliminating all other pollutants.
Test number 7: In this test, we only considered
NOx, eliminating all other pollutants that may be
present in the flue gas stream. So, in the reactor,
we have the kinetic reactions of NOx being
oxidised and then absorbed to prevent their
release directly into the atmosphere.
Although the most critical tests were mentioned
above, many other tests in Aspen are related to
changes in some parameters of currents or
devices.
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Some results and graphs generated by Aspen Plus
Fig. 12: Results when using reactions for SOx only
Fig. 13: Numerical calculations results for the reactor
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Fig.14: Results for the absorber
The following charts, 1-4, show the dependence
of mass and the number of plates in the column,
the dependence of mass on plates in different
phases, the dependence of temperature on plates,
and the dependence of temperature in the cooler,
respectively.
Chart 1: Mass and number of plates in the column
Graph 2: Dependence of mass on plates in
different phases
Graph 3: Dependence of temperature on plates
Graph 4: Dependence of temperature in the
cooler
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4. Conclusions and Recommendations
In anticipation of the calculated results that the
Aspen Plus program should have generated, it
should be within the expectations described in the
theory above. The NOx and SOx gases at the outlet
of the gas vapour stream at the outlet of the
absorber should have been sufficiently reduced
about the measures we have set at the inlet. Input
measures were taken from the literature, and some
reports and component measures were found from
the reactions. In conclusion, the polluting gas
should have been reduced so that after oxidation
with chlorine oxide and interaction with different
bases, they could form more salts dissolved in
water than components released in the gas
vapours from the absorber.
If the stream of gases released above the reactor
has more pollutants than the stream below the
reactor, then we have something that could have
been done better with the program, or that needs
to be added to our data. If the stream of salt
solutions has a large amount of pollution, it will
not be a problem since we can add a treatment
plant for these waters and make them harmless to
the environment.
Our interest is only in the one at the outlet of the
absorber gases, and there, we have to minimise
the components of NOx and SOx as much as
possible.
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Contribution of Individual Authors to the
Creation of a Scientific Article (Ghostwriting
Policy)
The authors equally contributed in the present
research, at all stages from the formulation of the
problem to the final findings and solution.
Sources of Funding for Research Presented in a
Scientific Article or Scientific Article Itself
No funding was received for conducting this study.
Conflict of Interest
The authors have no conflicts of interest to declare
that are relevant to the content of this article.
Creative Commons Attribution License 4.0
(Attribution 4.0 International, CC BY 4.0)
This article is published under the terms of the
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International Journal on Applied Physics and Engineering
DOI: 10.37394/232030.2024.3.9
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