期刊文献+

对位芳纶纤维及其打浆粉末端基结构的MALDI-TOF MS分析

Study on the End-group Structure of PPTA Fiber and Its Beating Powder by MALDI-TOF MS
下载PDF
导出
摘要 利用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)对两种对位芳纶短切纤维(A1-PPTA、A2-PPTA)及其打浆粉末的端基结构进行分析,通过谱图特征峰与端基结构的对应关系,分析端基结构与反应机理的关联性及打浆过程产生粉末的原因。结果显示,A1-PPTA和A2-PPTA的聚合过程均采用了近似等摩尔的反应物来控制聚合过程;A2-PPTA的聚合过程发生溶剂链转移的几率更高;A2-PPTA中存在较多不利于纤维强度的端基结构,导致其打浆过程中产生更多粉末。 Matrix-assisted laser desorption / ionization time-of-flight mass spectrometry( MALDI-TOF MS) was used to study the end-group structure of two kinds of poly( p-phenylene terephthalamide)-PPTA short-cut fiber( A1-PPTA fiber and A2-PPTA fiber) and the PPTA powder produced by beating the PPTA fibers during the paper-making process. The basic database of the spectral characteristic peak and the endgroup structure was established to reveal the relationship between the reaction mechanism and the end-group structure,and to find the producing causes of the PPTA powder during the beating process. The results showed that polymerization process for A1-PPTA fiber and A2-PPTA fiber were both carried out with an approximate equivalent amount of reactants. The probability of chain transferring to solvent in A2-PPTA fiber was higher than A2-PPTA fiber; The existing of more end-group structures which were not benefit to fiber's mechanical strength in A2-PPTA fiber caused more large amount of powder in the beating process.
出处 《中国造纸》 CAS 北大核心 2015年第10期30-35,共6页 China Pulp & Paper
关键词 基质辅助激光解吸电离飞行时间质谱 对位芳纶纤维 打浆粉末 端基结构 matrix-assisted laser desorption / ionization time-of-flight mass spectrometry(MALDI-TOF MS) PPTA fiber beating powder end-group structure
  • 相关文献

参考文献23

  • 1Langueranda D L, ZHANG B H, Murthycns, et 81. Inelastic behavior and fracture oflrighmodulus polymeric fiber bundles at high strain-rates [ J]. Materials Science and Engineering A, 2009, 500 : 216.
  • 2钱伯章.芳纶的国内外发展现状[J].化工新型材料,2007,35(8):26-27. 被引量:15
  • 3李金宝,张美云,吴养育.对位芳纶纤维结构形态及造纸性能[J].中国造纸,2004,23(10):54-57. 被引量:33
  • 4燕丰.国内外对位芳纶纤维开发及应用前景分析[J].中国石油和化工经济分析,2011(12):42-45. 被引量:6
  • 5Fitzgerald J A, Irwin R S, Memeger W. Synthesis of poly( p-phenyl- ene terephthalamide) by solid-phase polymerization [ J ]. Macromole- cules, 1991, 24(11) : 3291.
  • 6Mehenni H, Guillou H, Tessier C, et al. Effect of chain ends on the structure ofaramid oligomers[J]. Can. J. Chem. , 2008, 86(1) : 7.
  • 7Knijnenberg A, Bos J, Dingemans T J. The synthesis and eharacteri- sation ofreaetive poly ( p-phenylene terephthalamide ) s : A route to- wards compression stable aramidfibres [ J]. Polymer, 2010, 51 (9) : 1887.
  • 8Arpin M, Strazielle C. 6tude par chromatographie sur gel en phase liquided'6chantillons depolyamide aromatique de type poly [ imino- (ph6nylne-1,4)iminot6r6phtaloyle] [J]. Makromol. Chem., 1976, 177(1) : 293.
  • 9TAKATSUKA R, UNO K, TODAF, et al. Study on wholly aromatic polyamides containing methyl-substituted phenylene linkage [ J ]. J. Polym. Sei. : Polym. Chem. Ed. , 1977, 15(8) : 1905.
  • 10CHATFIELD D A, EINHORN I N, MICKELSON R W, et al. Analy- sis of the products of thermal decompositionof an aromatic polyamide fabric[ J]. J. Polym. Sci. : Polym. Chem. Ed., 1979, 17 (5) : 1367.

二级参考文献129

共引文献83

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部