Removal of Carbon Dioxide and Hydrogen Sulfide from Natural Gas Using a Hybrid Solvent of Monoethanolamine and N-Methyl 2-Pyrrolidone

被引:1
作者
Farooqi, Abid Salam [1 ,2 ]
Ramli, Raihan Mahirah [1 ,2 ]
Lock, Serene Sow Mun [1 ,3 ]
Farooqi, Ahmad Salam [4 ]
Shahid, Muhammad Zubair [4 ]
ul Hasnain, Syed Muhammad Wajahat [1 ,3 ]
Hira, Noor e [1 ,3 ]
Abdullah, Bawadi [1 ,3 ]
机构
[1] Univ Teknol PETRONAS, Dept Chem Engn, Seri Iskandar 32610, Perak, Malaysia
[2] Univ Teknol PETRONAS, Ctr Innovat Nanostruct & Nanodevices, Seri Iskandar 32610, Perak, Malaysia
[3] Univ Teknol PETRONAS, CO2 Res Ctr CO2RES, Seri Iskandar 32610, Malaysia
[4] King Fahd Univ Petr & Minerals, Interdisciplinary Res Ctr Hydrogen Technol & Carbo, Dhahran 31261, Saudi Arabia
来源
ACS OMEGA | 2024年 / 9卷 / 24期
关键词
CO2; CAPTURE; HIGH-PRESSURE; ABSORPTION PROCESS; SIMULATION; KINETICS; AMINES;
D O I
10.1021/acsomega.3c09100
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The main goal of traditional methods for sweetening natural gas (NG) is to remove hydrogen sulfide (H2S) and significantly lower carbon dioxide (CO2). However, when NG processes are integrated into the carbon capture and storage (CCS) framework, there is potential for synergy between these two technologies. A steady-state model utilizing a hybrid solvent consisting of N-methyl-2-pyrrolidone (NMP) and monoethanolamine (MEA) has been developed to successfully anticipate the CO2 and H2S capture process from NG. The model was tested against important variables affecting process performance. This article specifically explores the impact of operational parameters such as lean amine temperature, absorber pressure, and amine flow rate on the concentrations of CO2 and H2S in the sweet gas and reboiler duty. The result shows that hybrid solvents (MEA + NMP) perform better in removing acid gases and reducing reboiler duty than conventional chemical solvent MEA. The primary purpose is to meet product requirements while consuming the least energy possible, which is in line with any process plant's efficiency goals.
引用
收藏
页码:25704 / 25714
页数:11
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