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Preparation of PMAM-B-PNVP and its Hydrolysate by RAFT Polymerization: Structure Characterization and its CO_2 Permeation Performance

机译:通过筏聚合制备PMAM-B-PNVP及其水解产物:结构表征及其CO_2渗透性能

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Macromolecules chain transfer agents (MCTA) were synthesized through the reversible addition fragmentation chain transfer polymerization (RAFT) by using S-l-Dodecyl-S'-(α,α'-dimethyl-α-acetic acid) trithiocarbonate(MTTCD), S,S'-bis (2-hydroxyethyl-2'-dimethylacrylate) trihiocarbonate (BDATC), 2-cyanoprop-2-yl dithiobenzoate (CPDB) as the chain transfer agents, methacrylamide (MAM) as the first polymerization monomer. The results showed that the structures of the end-group of dithiocarbamates had significant effects on the activity of dithiocarbamates for the polymerization of PMAM. The derived block copolymer (PMAM-b-PNVP) was prepared by using the above mentioned polymer as macromolecular RAFT agent and NVP as the second polymerization monomer. N-vinyl-γ-sodium aminobutyrate-sodium methacrylate copolymer (VSA-MSA) containing -NH_2 and -COOH as the CO_2 facilitated carrier, a kind of new fixed carrier membrane material for CO_2 separation, was synthesized by hydrolysis of the resulted PMAM-b-PNVP. The chemical composition and structure of PMAM-CTA, PMAM-b-PNVP, MSA-VSA were analyzed by FTIR, ~1HNMR and DSC, the molecular weight and polydispersity index were analyzed by GPC. The Relative molecular mass of polymer was controllable. The polydispersity index (1.2~1.3) of the obtained polymer was narrow via using MTTCD and BDATC. The VSA-MSA/PS composite membranes were prepared. The CO_2 and N_2 permeation performance were tested at different pressure. The results showed that the resulted composited membrane had a CO_2 permeation rate of 1.2×10~(-4) cm~3 (STP) cm~(-2)s~(-1)cmHg~(-1) and a N_2 permeation rate of 8.57×10~(-7) cm~3 (STP) cm~(-2)s~(-1)cmHg~(-1) and an ideal CO_2/ N_2 selectivity of 140.02 at a feed gas pressure of 7.6 cmHg and 30 ?C.
机译:通过使用SL-十二烷基-S' - (α,α'-二甲基-α-乙酸)三碳酸酯(MTTCD),S,S,S,S,S,S,S,S,S,S,S '-Bis(2-羟基乙基-2'-二甲基丙烯酸酯)三碳酸酯(BDATC),2-氰基普洛-2-基二苯甲酸二苯甲酸酯(CPDB)作为链转移剂,甲基丙烯酰胺(MAM)作为第一聚合单体。结果表明,二硫代氨基甲酸酯端基的结构对PMAM聚合的二硫代氨基酯的活性有显着影响。通过使用上述聚合物作为大分子筏剂和NVP作为第二聚合单体,制备衍生的嵌段共聚物(PMAM-B-PNVP)。含有-NH_2和-COOH的N-乙烯基-γ-钠氨基丁酯 - 甲基丙烯酸钠共聚物(VSA-MSA)作为CO_2促进的载体,通过得到的PMAM水解合成了一种用于CO_2分离的新型固定载体膜材料 - B-PNVP。通过FTIR,〜1HNMR和DSC分析PMAM-CTA,PMAM-B-PNVP,MSA-VSA的化学组成和结构,分子量和多分散指数进行GPC分析。聚合物的相对分子量可控。通过使用MTTCD和BDATC,所得聚合物的多分散性指数(1.2〜1.3)窄。制备VSA-MSA / PS复合膜。在不同的压力下测试CO_2和N_2渗透性能。结果表明,得到的复合膜的CO_2渗透率为1.2×10〜(-4)cm〜3(STP)cm〜(-2)S〜(-1)CMHG〜(-1)和N_2渗透速率为8.57×10〜(-7)cm〜3(stp)cm〜(-2)s〜(-1)cmhg〜(-1)和140.02的理想CO_2 / n_2选择性,进给气体压力为7.6 cmhg和30?c。

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