Adsorption properties of benzene and water vapor on hyper-cross-linked polymers

被引:30
|
作者
Wang, Gang [1 ]
Dou, Baojuan [1 ]
Wang, Junhui [1 ]
Wang, Wanqiu [2 ]
Hao, Zhengping [1 ]
机构
[1] Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Beijing 100085, Peoples R China
[2] Shaanxi Normal Univ, Key Lab Appl Surface & Colloid Chem, Xian 710062, Peoples R China
来源
RSC ADVANCES | 2013年 / 3卷 / 43期
基金
国家高技术研究发展计划(863计划);
关键词
VOLATILE ORGANIC-COMPOUNDS; CRAFTS MODIFIED POLYSTYRENES; ACTIVATED CARBON; EFFICIENT REMOVAL; HYPERCROSSLINKED POLYSTYRENE; SBA-15; MATERIALS; EMERGING CLASS; SURFACE-AREA; DESORPTION; PERFORMANCE;
D O I
10.1039/c3ra41450g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of hyper-cross-linked polymers (HCPs) was synthesized via a post-cross-linking reaction using low-cross-linked polydivinylbenzene (PDVB) as precursor and 4,40-bis(chloromethyl)biphenyl (BCMBP) as cross-linking reagent. The effects of various amounts of BCMBP on the structures of the hyper-cross-linked polymers were discussed. The resultant typical HCP-1.3 possesses hierarchical micro/meso pore structures and a high stability up to 400 degrees C. The increased specific surface area and total pore volume of HCP-1.3, which reach 1231 m(2) g(-1) and 1.99 cm(3) g(-1), respectively, imply the high cross-linking ability of BCMBP. In order to study the adsorption properties of HCP-1.3, benzene and water were selected as typical adsorbates for their non-polar and polar characteristics. The static adsorption amount of benzene on HCP-1.3 is 30.0 mmol g(-1), which is two times higher than the corresponding adsorbed water amount, suggesting a potential hydrophobic property of HCP-1.3. Dynamic adsorption was performed with a fixed-bed column to simulate the real situation under dry and 30% relative humidity conditions. The results show the dynamic adsorption amount under the 30% relative humidity condition is as high as 90% of the value under dry conditions, implying HCP-1.3 would be a promising adsorbent for VOC adsorption under both dry and humid conditions.
引用
收藏
页码:20523 / 20531
页数:9
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