应用化学

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聚2,5-呋喃二甲酸1,8-辛二酯的聚合反应

李连贵1,李洋1,叶冲2,张强2,姜敏2,周光远2,3*   

  1. (1.长春工业大学化学与生命科学学院 长春 130012;
    2.中国科学院长春应用化学研究所生态环境高分子材料重点实验室 长春 130022;
    3.常州储能材料与器件研究院 常州 213002)
  • 收稿日期:2012-12-17 修回日期:2013-02-05 出版日期:2013-06-10 发布日期:2013-06-10
  • 通讯作者: 周光远,研究员; Tel:0431-85262796; Fax:0431-85685653; E-mail:gyzhou@ciac.jl.cn; 研究方向:聚烯烃可控聚合及生物聚酯
  • 基金资助:
    国家自然科学基金青年科学基金资助项目(51103152)

Synthesis of Poly(octylene 2,5-furandicarboxylate)

LI Liangui1, LI Yang1, YE Chong2, ZHANG Qiang2, JIANG Min2, ZHOU Guangyuan2,3*   

  1. (1.College of Chemistry and Life Sciences,Changchun University of Technology,Changchun 130012,China;
    2.Key Laboratory of Polymer Ecomaterials,Changchun Institute of Applied Chemistry,
    Chinese Academy of Scineces,Changchun 130022,China;
    3.Changzhou Institute of Energy Storage Materital & Devices,Changzhou 213002,China)
  • Received:2012-12-17 Revised:2013-02-05 Published:2013-06-10 Online:2013-06-10

摘要: 以可再生资源2,5-呋喃二甲酸(FDCA)和1,8-辛二醇(1,8-ODO)为原料,钛酸四丁酯为催化剂,采用直接酯化法制得聚2,5-呋喃二甲酸1,8-辛二酯(1,8-POF)。 考察了原料配比、催化剂用量、酯化温度、缩聚温度及缩聚时间对聚合反应的影响,结果表明,当n(FDCA)∶n(1,8-ODO)=1∶1.2,钛酸四丁酯摩尔分数为0.3%,酯化温度为240 ℃,缩聚温度为260 ℃,缩聚时间为300 min时,缩聚产物的比浓粘度最高(2.1 dL/g),端羧基含量最低(5.8 mol/t)。 与乙二醇相比,采用1,8-辛二醇为单体降低了酸醇的摩尔比,减少了醇的消耗,同时得到了较高分子量的聚合物。 气质联用仪对酯化馏出液和缩聚产物真空抽出物进行了分析,结果表明,酯化馏出液的主要成分是水,并含有少量的1,8-ODO;缩聚产物真空抽出物的组成为环己酮(56%)、顺式-3-辛烯醇(18%)、4-甲基-3-戊烯-2-酮(17%)和4-羟基-4-甲基-2-戊酮(9%)。

关键词: 聚呋喃二甲酸-辛二酯, 呋喃二甲酸, 直接酯化法, 可再生资源, 聚合反应

Abstract: Poly(octylene 2,5-furandicarboxylate)(POF) was synthesized via the direct esterification method starting from 2,5-furandicarboxylic acid(FDCA) and 1,8-octylene glycol(1,8-ODO), in which tetrabutyl titanate was chosen as catalyst. Effect of the molar ratio of F-DCA to 1,8-ODO, dosage of tetrabutyl titanate, esterification temperature, polycondensation temperature on the esterification and polycondensation processes were studied in details. The optimized process conditions are:n(FDCA)∶n(1,8-ODO)=1∶1.2, tetrabutyl titanate dosage is 3×10-3 mol/mol FDCA, esterification temperature is 240 ℃, polycondensation temperature is 260 ℃, polycondensation time is 300 min. The relative molecular mass of the condensation product is the highest(ηSP/ρ=2.1 dL/g), and the carboxylic group content is the lowest(5.8 mol/t). Compared with ethylene glycol, using the 1,8-ODO reduced the molar ratio of FDCA to 1,8-ODO, and reduced the consumption of alcohol, meanwhile we got a high molecular mass polymer. The results of gas chromatography mass spectrometry(GC-MS) confirmed the composition of the esterification distillate and polycondensation product extractives. The results were found to be: the main ingredient of esterification distillate is H2O, and the other component is 1,8-ODO; polycondensation product extractives are composed of cyclohexanone (56%), (Z)-3-octene alcohol(18%), 4-methyl-3-amylene-2-ketone(17%), 4-hydro-xy-4-methyl-2-pentan-one(9%).

Key words: Poly(octylene furandicarboxylate), furandicarboxylic acid, direct esterification method, renewable resources, polymerization reaction

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