熔盐
煅烧
碱金属
吸附剂
熔点
化学工程
吸附
傅里叶变换红外光谱
扫描电子显微镜
二氧化碳
无机化学
碳酸盐
解吸
盐(化学)
化学
材料科学
有机化学
催化作用
工程类
复合材料
作者
Liang Huang,Yu Zhang,Wanlin Gao,Takuya Harada,Qingqing Qin,Qianwen Zheng,T. Alan Hatton,Qiang Wang
标识
DOI:10.1002/ente.201600628
摘要
Abstract CO 2 reduction is crucial if the effects of this gas on global warming are to be alleviated. We report for the first time an alkali carbonate molten salt promoted CaO‐based CO 2 sorbent with CO 2 capture performance superior to that of neat CaO. The influences of chemical composition, loading, and melting temperature of the (Li–Na–K) 2 CO 3 molten salts and of the calcination and adsorption temperatures on CO 2 capture were evaluated systematically. The microstructural and morphological evolution of the samples during CO 2 adsorption was studied by X‐ray diffraction, scanning electron microscopy, and Fourier‐transform infrared spectroscopy analyses. The (Li–K) 2 CO 3 molten salt coating was found not only to promote CO 2 uptake but also to facilitate CO 2 desorption from CaO. In particular, at low temperatures of 500 and 600 °C, the CO 2 capture capacity increased significantly from 1.19 and 3.26 mmol g −1 to 6.93 and 10.38 mmol g −1 , respectively. The melting point of the molten salts was also a crucial factor in the improvement of CO 2 uptake. Kinetic studies based on fractal‐like models indicated that the rate coefficients for (Li–K) 2 CO 3 /CaO were approximately 3.3 to 3.8 times larger than those for neat CaO. The coating of alkali carbonate molten salts is believed to prevent the formation of a rigid CaCO 3 layer on the surface of the CaO particles and to provide continuous delivery of CO 3 2− to promote CO 2 capture. During the CO 2 adsorption/desorption cycling tests, (Li–K) 2 CO 3 /CaO resulted in a stable and reversible CO 2 uptake of 6.0–6.3 mmol g −1 , which is much higher than that of neat CaO (2.0 mmol g −1 ).
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