Rapid CO2 capture from ambient air by sorbent-containing porous electrospun fibers made with the solvothermal polymer additive removal technique

被引:27
作者
Armstrong, Mitchell [1 ]
Shi, Xiaoyang [1 ]
Shan, Bohan [1 ]
Lackner, Klaus [1 ]
Mu, Bin [1 ]
机构
[1] Arizona State Univ, Sch Engn Matter Transport & Energy, Chem Engn, Tempe, AZ 85287 USA
基金
美国国家科学基金会;
关键词
adsorption/gas; electrospinning; electrospun nanofiber nanoparticle composites; moisture or humidity swing; direct air capture of CO2; CARBON-DIOXIDE; ADSORPTION; ADSORBENTS; SORPTION;
D O I
10.1002/aic.16418
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Direct air capture (DAC) of CO2 is an emerging technology in the battle against climate change. Many sorbent materials and different technologies such as moisture swing sorption have been explored for this application. However, developing efficient scaffolds to adopt promising sorbents with fast kinetics is challenging, and very limited effort has been reported to address this critical issue. In this work, the availability and kinetic uptake of CO2 in sorbents embedded in various matrices are studied. Three scaffolds including a commercially available industrial film containing ion-exchange resin (IER), IER particles embedded in dense electrospun fibers, and IER particles embedded in porous electrospun fibers are compared, in which a solvothermal polymer additive removal technique is used to create porosity in porous fibers. A frequency response technique is developed to measure the uptake capacity, sorbent availability, and kinetic uptake rate. The porous fiber has 90% IER availability, while the dense fibers have 50% particle accessibility. The sorption half time for both electrospun fiber samples is 10 +/- 3 min. Our experimental results demonstrate that electrospinning polymer/sorbent composites is a promising technology to facilitate the handleability of sorbent particles and to improve the sorption kinetics, in which the IER embedded in porous electrospun fibers shows the highest cycle capacity with an uptake rate of 1.4 mol CO2 per gram-hour. (c) 2018 American Institute of Chemical Engineers AIChE J, 65: 214-220, 2019
引用
收藏
页码:214 / 220
页数:7
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