热重分析
傅里叶变换红外光谱
聚合物
吸附
超临界流体
化学
化学工程
高分子化学
甲基丙烯酰胺
材料科学
核化学
有机化学
单体
工程类
丙烯酰胺
作者
Kehinde A. Fayemiwo,Goran T. Vladisavljević,Seyed Ali Nabavi,Brahim Benyahia,Dawid P. Hanak,Konstantin N. Loponov,Vasilije Manović
标识
DOI:10.1016/j.cej.2017.11.106
摘要
A series of poly[methacrylamide-co-(ethylene glycol dimethacrylate)] (poly(MAAM-co-EGDMA)) porous polymeric particles with high CO2-philicity, referred to as HCP-MAAMs, were synthesised for CO2 capture. The polymers with a MAAM-to-EGDMA molar ratio from 0.3 to 0.9 were inherently nitrogen-enriched and exhibited a high affinity towards selective CO2 capture at low pressures. A techno-economic model based on a 580 MWel supercritical coal-fired power plant scenario was developed to evaluate the performance of the synthesised adsorbents. The presence and density of NH2 moieties within the polymer network were determined using Fourier transform infrared (FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS). The thermogravimetric analysis (TGA) showed that the polymers were thermally stable up to 515–532 K. The maximum CO2 adsorption capacity at 273 K was 1.56 mmol/g and the isosteric heat of adsorption was 28–35 kJ/mol. An increase in the density of amide groups within the polymer network resulted in a higher affinity towards CO2 at low pressure. At a CO2:N2 ratio of 15:85, CO2/N2 selectivity at 273 K was 52 at 1 bar and reached 104 at ultra-low CO2 partial pressure. The techno-economic analysis revealed that retrofitting a HCP-MAAM-based CO2 capture system led to a net energy penalty of 7.7–8.0%HHV points, which was noticeably lower than that reported for MEA or chilled ammonia scrubbing capture systems. The specific heat requirement was superior to the majority of conventional solvents such as MDEA-PZ and K2CO3. Importantly, the economic performance of the HCP-MAAM retrofit scenario was found to be competitive to chemical solvent scrubbing scenarios.
科研通智能强力驱动
Strongly Powered by AbleSci AI