Microporous organic polymers synthesized by self-condensation of aromatic hydroxymethyl monomers

被引:127
作者
Luo, Yali [1 ]
Zhang, Shoucun [1 ]
Ma, Yunxiang [2 ]
Wang, Wei [2 ]
Tan, Bien [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Wuhan 430074, Peoples R China
[2] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
基金
美国国家科学基金会;
关键词
TRIAZINE-BASED FRAMEWORKS; CO2; ADSORPTION; SURFACE-AREA; INTRINSIC MICROPOROSITY; FORMALDEHYDE RESINS; DESIGNED SYNTHESIS; CARBON-DIOXIDE; HYDROGEN; NETWORKS; STORAGE;
D O I
10.1039/c2py20914d
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Two hypercross-linked polymer networks have been synthesized by the self-condensation of bishydroxymethyl monomer, 1,4-benzenedimethanol (BDM), and monohydroxymethyl compound, benzyl alcohol (BA). This is different from the previous reports where multifunctional monomers or cross-linkers are crucial for constructing the porous polymer networks. N-2 sorption isotherms for the polymers show that both materials are predominantly microporous with Brunauer-Emmett-Teller (BET) surface areas of 847 m(2) g(-1) for HCP-BDM and 742 m(2) g(-1) for HCP-BA. A network based on BA can also store a significant amount of CO2 (8.46 wt%) and H-2 (0.97 wt%) at 1.0 bar, and at 273 K and 77 K respectively, despite its relatively modest surface area. Based on these results, this study opens up the possibility of synthesizing porous materials using monofunctional monomers.
引用
收藏
页码:1126 / 1131
页数:6
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