吸附
化学
缩水甘油
胺气处理
烷基
氨基甲酸
胺化
尿素
聚合物
戊二醛
高分子化学
多胺
有机化学
化学工程
催化作用
工程类
生物化学
作者
Hui He,Tang Han-ying,Xingjuan Chen,Xudong Hou,Xiaochong Zhou,Hong Chen,Shanyan Wu,Shuangfei Wang
出处
期刊:Langmuir
[American Chemical Society]
日期:2018-11-05
卷期号:34 (47): 14169-14179
被引量:16
标识
DOI:10.1021/acs.langmuir.8b02493
摘要
A novel low-temperature regenerative hydroxy-functionalized hyperbranched polyamine adsorbent (0.16OH-HBPA) for CO2 capture was readily prepared using glutaraldehyde to cross-link amino-terminated hyperbranched polymers (HBP) and functionalized with glycidol, followed by the reduction of the imino groups of 0.16OH-HBPA to alkyl aminos using NaBH4. Here, the HBP has been prepared through the one-pot reaction between pentaethylenehexamine and methyl acrylate. The as-prepared 0.16OH-HBPA adsorbent showed a high adsorption capacity (4.05 mmol/g) for CO2 (concentration, 10%) in the presence of water at 25 °C, and the alkyl amino utilization efficiency reached 73%. More importantly, the CO2-adsorbed 0.16OH-HBPA showed excellent regenerative performance at low temperatures (85 °C, under pure CO2 gas) due to the introduced hydroxyl that can cooperatively adsorb CO2 via the amino groups to form stable carbamic acid. This process suppressed the formation of open-chain urea and cyclic urea and could overcome the disadvantages of high regeneration temperatures (≥90 °C, under pure inert gas) of CO2-adsorbed traditional solid amine adsorbents.
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