Volume 43 Issue 12
Dec.  2015
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KONG Tong-tong, WANG Xia, GUO Qing-jie. Preparation and CO2 adsorption performance of a novel hierarchical micro/mesoporous solid amine sorbent[J]. Journal of Fuel Chemistry and Technology, 2015, 43(12): 1489-1497.
Citation: KONG Tong-tong, WANG Xia, GUO Qing-jie. Preparation and CO2 adsorption performance of a novel hierarchical micro/mesoporous solid amine sorbent[J]. Journal of Fuel Chemistry and Technology, 2015, 43(12): 1489-1497.

Preparation and CO2 adsorption performance of a novel hierarchical micro/mesoporous solid amine sorbent

Funds:  The project was supported by the National Natural Science Foundation of China (21276129) and Qingdao Application Foundation Research Project (14-2-4-5-jch).
  • Received Date: 2015-07-07
  • Rev Recd Date: 2015-09-15
  • Publish Date: 2015-12-30
  • The mixed supports were obtained at different weight ratios of HZSM-5 to MCM-41 by physical mixing processes. Tetraethylenepentamine (TEPA) modified mixed supports sorbents were prepared by the impregnation method. The sorbents were characterized by nitrogen adsorption/desorption, Fourier transform infrared spectroscopy (FT-IR) and thermogravimetric analysis (TGA) techniques. The effects of mixing ratios of HZSM-5 to MCM-41, TEPA loadings, adsorption temperatures, influent velocities, and CO2 partial pressures on CO2 adsorption capacity were investigated in a fixed bed reactor. It showed that the maximum CO2 adsorption capacity was 3.57 mmol/g of HZSM-5/MCM-41-30%TEPA at the adsorption temperature of 55℃ and influent velocity of 30 mL/min. After ten-cycles, the CO2 adsorption capacity decreased by 8.1%. CO2 adsorption was determined by a two-stage process, a fast breakthrough adsorption and a gradual approaching equilibrium stage. Moreover, the breakthrough adsorption capacity accounted for approximately 80% of the equilibrium adsorption capacity. The Avrami model could fit well with the experimental data of HZSM-5/MCM-41-30%TEPA. It illustrated that the adsorption mechanism was dominated by both chemical and physical adsorption.
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