Development Design of Amine Sweetening Unit Plant of Natural Gas
Development Design of Amine Sweetening Unit Plant of Natural Gas
Development Design of Amine Sweetening Unit Plant of Natural Gas
https://doi.org/10.22214/ijraset.2022.46548
International Journal for Research in Applied Science & Engineering Technology (IJRASET)
ISSN: 2321-9653; IC Value: 45.98; SJ Impact Factor: 7.538
Volume 10 Issue IX Sep 2022- Available at www.ijraset.com
Abstract: In addition to reduced equipment sizes, lower circulation rates, and greater overall amine concentration, selective
amines have become more popular for gas sweetening. Selective amines absorb H2S from CO2 through thermodynamic or
kinetic processes. Selective amine mixtures may enable a small quantity of CO2 to remain in the treated gas. Plant capacity
margins for selective amine units are frequently small. Increasing the acid gas concentration or throughput might result in sweet
gas that does not fulfill CO2 specifications. Increasing the amine concentration, employing combinations of amines, and altering
the lean amine temperature were explored since adding new equipment may be costly. Compared to increasing reboiler or
pumping capacity, these factors need little or no extra capital.
Keywords: Amine, Sweetening, Natural Gas, Plant, Development, CO2, Design, H2S
I. INTRODUCTION
The literature has extensively explored amine unit optimization. Selection of amines (Polasek and Bullin, 1984), plant configuration
(Polasek et al., 1983), and amine-water or other physical solvent mixes (Polasek et al. 1992; Okimoto, 1993). The authors
acknowledge the value of preferential amines in the gas sweetening sector.
Selective amines prefer H2S over CO2. Many writers believe that this preference arises from variations in solubility, reaction
speeds, or both (Barth et al., 1981, Cornelissen, 1982, and Danckwerts, 1979). The rate of reaction for CO2 reduces with
substitution on the nitrogen group, therefore primary amines react quicker than secondary and tertiary amines (Bullin et al., 1982).
Because H2S reacts so quickly, equilibrium is essentially attained for all amines. Primary amines are too rapid for selective
commercial sweetening units; nevertheless, secondary and tertiary amine selective units are commonly constructed to harness this
potential.
The introduction of selective amine treatment units increased plant efficiency. The industry embraced this new technology quickly
due to its economic benefits. In normal operation, methanolamine (MEA) and diglycolamine (DGA) absorb CO2 as fully as H2S.
Dietertiary amines such as DEA, DIPA, and MDEA are selective amines best used at high pressure (> 300 psi, 20 kPa). To increase
selectivity using selective amines, researchers examined low molecular weight sterically hindered amines with selectivity
comparable to MDEA (Sartori and Savage, 1983).
Selective amines allow for smaller equipment and circulation rates. Denny Law (1994) recently reported how employing MDEA
mixes reduced the predicted tray count for an acid gas standard. The CO2 absorption by extra trays may actually raise H2S content
in the sweetened gas Adding stages seems to increase CO2 absorption, displacing H2S. Because selective amines have lower
reaction temperatures than non-selective amines, regeneration takes less energy and smaller reboilers. Selective amines seldom
create caustic salts.
The use of selective amines, particularly MDEA, has spawned a new industry of "specialty" amines. Companies including BASF,
Dow, Huntsman Chemical, Shell, and Union Carbide produce MDEA-based specialized amines to boost or "customize" the amine's
sweetening capabilities. Shell combines sulfolane with MDEA or DIPA to generate Sulfinol, which enhances mercaptan and COS
removal (Okimoto, 1993). Increasing the performance of these "specialized" amine units has been documented. Huffmaster and
Nasir (1995) compare circulation rate and steam usage in amine and Sulfinol plants.
Numerous seminars and articles have addressed amine unit efficiency. Keller et al. (1995) report an industry conference that
reviewed amine process operations, issues, and solutions.
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International Journal for Research in Applied Science & Engineering Technology (IJRASET)
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This study found that amine losses, solution contamination, and off-spec products were the main causes of inefficient units.
Surprisingly, the amine type had no effect on efficiency or operability of MEA, DEA, and MDEA units.
Abry and Dupart (1995) provide great advice for improving amine plants using historical data. According to the authors, this process
knowledge helps regulate and avoid disturbances. Away from design circumstances, the authors explain how this plant data may be
utilized to improve the facility's performance. The optimization in this reference used a lower intake gas flow rate with the same
acid gas content. With larger concentrations of acid gas components, their analysis proved impractical and maybe unduly optimistic.
Concerned about amine unit efficiency, most current work discusses employing plant data or proprietary "specialty" amines. This is
incredibly helpful yet incomplete information. Few recent research discuss process simulators in amine unit optimization. This is
concerning as amine sweetening simulations get more accurate. Engineers may utilize these technologies to identify optimal plant
operating parameters. An optimization study may look at alternate amines, amine mixes, absorber equilibrium phases, or regenerator
reboiler duties. In an active facility, acquiring plant data for different amines or equilibrium phases is difficult. But process
simulation can readily study these situations.
This research uses the TSWEET® process simulator. This program's accuracy has been shown for single amines (MacKenzie et al.,
1987) and amine combinations (Spears et al., 1996). There are two acid gas models: Kent and Eisenberg (1976) and NRTL (Chen
and Evans, 1986). All simulations and computations in this work employed the NRTL model. Other sites provide details on the
program's calculations (Bullin et al., 1981).
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International Journal for Research in Applied Science & Engineering Technology (IJRASET)
ISSN: 2321-9653; IC Value: 45.98; SJ Impact Factor: 7.538
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Table 1 displays the facility's design and current operating characteristics. The operators were worried that the sweet gas exceeded
CO2 specifications, so they made alterations. Spears et al. (1996) explain the facility and how the process simulator TSWEET fits
the plant data for DEA and MDEA/DEA. 0.35% CO2 is the design parameter. Figure 2 compares simulation results to plant data for
a 32 wt% DEA solution and a 32 wt% DEA/13 wt% MDEA combination. This value provides a benchmark for simulation accuracy.
Fig. 2. Data from plants and TSWEET findings for CO2 content in sweet gas for single and mixed amines.
The simulator was used to study amine concentration, mixed amine system, and lean amine temperature. These variables may be
changed without adding new equipment or increasing current equipment. If the facility is presently at capacity, raising circulation
rates, stripping steam, or the number of equilibrium stages may need capital expenditure.
Bullin et al. (1989) address MDEA CO2 removal temperature. This study examines a low and high CO2 intake gas stream. Boosting
the trim cooler temperature from 311 to 328K (100 to 130°F) enhanced CO2 absorption in both situations. As the solubility
decreases, the amount of CO2 absorbed decreases. It seems that the maximum temperature is dependent on amine concentration,
incoming acid gas concentration, and contactor acid gas absorption. Sadly, no comparable statistics were available at the time.
The sample facility detailed here is not indicative of general circumstances, since there is no such thing as a "general case" in gas
processing. Each instance must be evaluated individually owing to the diverse circumstances and needs of gas processing plants.
Engineers cannot control certain factors like incoming gas flow rate and composition. Moreover, each sweetening unit's goal may
vary depending on the final destination of the sweetened gas. A facility's incoming gas composition and flow rate may be same. One
facility may be able to sneak as much CO2 as feasible whereas another may have rigorous CO2 concentration limits. H2S must be
accomplished in any instance. Each of these equipment should be developed differently to maximize the goal.
A. Concentration of Amine
The amine concentration may be increased easily. However, rust makes this impractical. Due to high primary and secondary amine
concentrations, the lean/rich exchanger and reboiler suffer from significant corrosion. Figure 3 displays CO2 and H2S
concentrations as a function of amine weight percent. The process variables DEA, DIPA, and MDEA were kept constant.
Fig. 3. Calculated findings for CO2/H2S concentration in the sweet gas for DEA, DIPA, and MDEA as a function of amine weight
% amine.
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With rising DEA content, CO2 and H2S concentrations declined. With rising amine concentrations, CO2 concentrations declined
while H2S concentrations remained stable. The extra CO2 these amines absorb tends to displace the H2S. For all amines examined,
the H2S content was well within specification.
According to Figure 3, DEA at 40% or more is necessary to remove the acid gas. At such concentration, DEA tends to take up a lot
of acid vapors, potentially caustic. Increasing the amine concentration is not an option here.
B. Mixtures of Amine
Since increasing concentration of a single amine could not fulfill the CO2 standard, amine combinations were investigated. A 30
wt% DEA solution is shown in Figure 4 with the CO2 content in the sweet gas changing when MDEA is added. H2S concentrations
were significantly below specification. All other process variables were kept constant. Because MDEA is less corrosive than DEA,
larger amine concentrations may be employed. The facility met specification with 5% MDEA; 10% MDEA provided a safety buffer.
It may seem counterintuitive to add an amine renowned for sliding CO2 to boost CO2 pickup. However, adding MDEA raises overall
amine levels.
Fig. 4. Calculated findings for CO2 concentration in the sweet gas for DEA/MDEA mixture
Figure 5 shows the concentration of CO2 in DEA and DEA/MDEA mixtures. Assumed 12/94 input circumstances for DEA; dashed
line 2/95 input conditions. The slope of the pure DEA line is larger than the slope of the MDEA/DEA combination, indicating that
DEA alone has a stronger propensity to absorb CO2. Using MDEA enhances amine concentration and reduces heat of absorption
while being less corrosive.
Fig. 5. Comparison between calculated findings for CO2 concentration in the sweet gas for DEA and DEA/MDEA mixture
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International Journal for Research in Applied Science & Engineering Technology (IJRASET)
ISSN: 2321-9653; IC Value: 45.98; SJ Impact Factor: 7.538
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Fig.6. CO2 content in the sweet gas per unit volumetric flow rate of intake gas for single amines and amine combinations
So, for a given volume of intake gas flow rate, Figure 6 depicts CO2 concentration in the sweet gas per volume inlet gas flow rate.
Data shows that trim cooler temperature affects selective amine CO2 absorption. Also, at 314-331K (105-135°F) temperatures, the
CO2 content in the sweet gas falls as the lean temperature rises. To test how lean amine temperature influences CO2 composition in
sweet gas, the simulator kept all other process variables constant. Adjustments are made to duty in the lean amine cooler, as well as
amine and water makeup.
On the other hand, DEA (32 wt%) has a higher acid gas concentration in the sweet gas (Figure 7). Due to diminishing solubility, the
concentration of H2S grows monotonically with colder temperature. The H2S specification is met at 336K (145°F) lean amine
temperatures. The sweet gas CO2 concentration is lowest at 322K (120°F) lean amine temperature. The kinetic effect increases with
temperature, while solubility decreases. After a certain temperature, solubility trumps kinetics. Notably, the CO2 concentration never
falls below 0.35 mole percent.
Fig.7. Calculated CO2 and H2S proportions in the sweet gas as a procedure of lean amine temperature for 32 wt % DEA
From 311 to 336K (100-145°F), Figure 8 shows the comparison of DEA, DIPA, and MDEA at 32 wt%. Dat DIPA and MDEA are
more selective or kinetically regulated than DEA. From 311 to 327K (100 to 130°F), MDEA exhibits a 40% reduction in CO2
concentration. Notably, the 32 wt% DIPA and MDEA cross at 322K (120°F). DIPA absorbs more CO2 than MDEA at lower
temperatures but less at higher temperatures. Nevertheless, neither MDEA nor DIPA at 32 wt% absorb enough CO2.
Fig. 8. Calculated CO2 concentrations in the sweet gas versus lean amine temperature for DEA, DIPA, and MDEA at 32 wt %
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Water and amine losses should rise with lean amine temperature. Amine losses increased from 311 to 333K (100 to 140°F) for DEA,
DIPA, and MDEA. Figure 9 shows that water losses rose by a factor of 6. The simulator findings show that most water loss happens
in the absorber when the sweet gas departs saturated. Minimal flash tank and stripper losses
Fig. 9. Calculated water makeup vs. lean amine temperature for 32 wt % DEA, DIPA, and MDEA
Next, amine mixes and lean amine temperatures were explored. The starting point was 30% DEA. The MDEA concentration was
raised to 30% with the same circulation rate. From 311 to 336K (100-145°F), the lean amine temperature. The CO2 concentration in
the sweet gas was the main worry as the single amine concentrations met the H2S criteria. Increasing the MDEA concentration in the
solution reduces the CO2 content in the sweet gas. Additional MDEA after 25% wt% seems to have minimal impact on CO2 uptake.
Less clear, however, is the influence of wt % MDEA on the minimum CO2 concentration in the sweet gas. The lowest concentration
of DEA is at 322K (120°F). The lowest is 319K (115°F) with 5% MDEA. The lowest temperature rises with MDEA content.
Fig.10. Calculated CO2 concentrations in sweet gas for 30 wt % DEA based on lean amine temperature and wt % MDEA
This research focused on the influence of lean amine temperature on selective amine CO2 pickup, although the reverse may be
investigated. The operator may enhance CO2 slip by lowering the lean amine temperature or precooling the intake gas.
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International Journal for Research in Applied Science & Engineering Technology (IJRASET)
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If the base or stock solution is MDEA, the only amine combination to select is MEA or DEA. These amines boost CO2 uptake but
have greater absorption temperatures and are more corrosive than MDEA. Undersized reboilers may cause issues. Finally, raising
the lean amine temperature enhances CO2 pickup, but only to a point. Amount of CO2 uptake and amine concentration affect this
temperature. Heat reduces H2S uptake and increases amine and water losses. They must be checked.
IV. CONCLUSIONS
The ultimate purpose of amine sweetening is to manufacture goods of high quality at low cost. It has created selective absorbents
that remove H2S when CO2 is present. Selective amines reduce circulation rates, reboiler sizes, and responsibilities while achieving
H2S requirements. Due to changes in intake composition or higher throughput, several operators now exceed the CO2 standard in
sweet gas streams. Complying with the process equipment limits is the most economical and desired option.
The amine sweetening unit was analyzed using TSWEET for amine concentration, amine mixes, and lean amine temperature.
Increasing amine concentration is beneficial if it does not exceed corrosion limitations. It seems that using amine combinations
would increase CO2 uptake for DEA and MDEA based solutions. Finally, using selective amines like DEA, DIPA, and MDEA, the
lean amine temperature may be changed to reduce CO2 content in the sweet gas. The improvement depends on amine concentration
but may reach 20%. As a consequence, lesser H2S collection and greater water losses from the absorber occur.
To accomplish the H2S criterion, the engineer should use the most preferential amine at the lowest concentrations and circulation
rate feasible. Cold absorber temperatures promote CO2 slip and H2S pickup. The issue becomes more complex if the goal is to
reach a specified CO2 concentration. Consider raising the amine concentration or employing amine mixes.
It may be necessary to adjust equipment size. Increasing the temperature of the selective amines boosts CO2 pickup. Inlet gas mix
and loading affect maximum temperature. Water and amine losses rise with temperature, but H2S uptake decreases.
V. ACKNOWLEDGEMENT
Financial support for this study was provided by Kalo Oil & Gas Ltd and Golden Fortitude Oil & Gas. The authors wish to thank
Engr. Johnson Nnadikwe for his contributions on preparing the research work.
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