Adsorption properties of benzene and water vapor on hyper-cross-linked polymers
Author(s) -
Gang Wang,
Baojuan Dou,
Junhui Wang,
Wanqiu Wang,
Zhengping Hao
Publication year - 2013
Publication title -
rsc advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.746
H-Index - 148
ISSN - 2046-2069
DOI - 10.1039/c3ra41450g
Subject(s) - adsorption , benzene , relative humidity , polymer , water vapor , reagent , biphenyl , chemistry , chemical engineering , volume (thermodynamics) , polar , chemical polarity , polymer chemistry , materials science , organic chemistry , thermodynamics , molecule , engineering , physics , astronomy
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 4,4′-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 °C. The increased specific surface area and total pore volume of HCP-1.3, which reach 1231 m2 g-1 and 1.99 cm3 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. © The Royal Society of Chemistry 2013.
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