Synthesis and characterization of phenylethynylcarbonyl terminated novel thermosetting imide compound

被引:9
作者
Kimura, H. [1 ]
Ohtsuka, K. [1 ]
Matsumoto, A. [1 ]
Fukuoka, H. [2 ]
Oishi, Y. [3 ]
机构
[1] Osaka Municipal Tech Res Inst, Organ Mat Res Div, Thermosetting Resin Lab, Joto Ku, Osaka 5368553, Japan
[2] Mitsubishi Gas Chem Co Inc, Div Res & Dev, Chiyoda Ku, Tokyo 1008324, Japan
[3] Iwate Univ, Fac Engn, Dept Chem & Bioengn, Morioka, Iwate 0208550, Japan
来源
EXPRESS POLYMER LETTERS | 2013年 / 7卷 / 02期
关键词
thermosetting resins; imide; phenylethynylcarbonyl; DYNAMIC MECHANICAL PROPERTIES; EPOXY-RESINS; POLYIMIDES; TEMPERATURE; IMIDIZATION; POLYMERS; DIAMINE; DESIGN;
D O I
10.3144/expresspolymlett.2013.15
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Phenylethynyl terminated novel imide compound based on 1,3-bis(3-aminophenoxy)benzene (APB) and phenylethynyl trimellitic anhydride (PETA) were prepared. The curing behavior of phenylethynyl terminated imide compound was investigated by differential scanning calorimetry and Fourier transform infrared spectrometry. The curing reaction of phenylethynylcarbonyl end group completed at 220 degrees C, and proceeded much faster than that of phenylethynyl end group. Glass transition temperature of the thermosetting resin from phenylethynylcarbonyl terminated novel imide compound determined by dynamic mechanical analysis was almost the same as that of o-cresolnovolac type epoxy resin. In addition, the thermosetting resin from phenylethynylcarbonyl terminated novel imide compound exhibited excellent thermal and dimensional stabilities. These excellent properties of these phenylethynyl terminated imide compound might be due to the incorporation of alkene group or aromatic ring substitutes in the backbones, which might enhance the chain interaction (molecular packing) and reduce the molecular chain mobility.
引用
收藏
页码:161 / 171
页数:11
相关论文
共 20 条
[1]   Soluble polyimides from unsymmetrical diamine containing benzimidazole ring and trifluoromethyl pendent group [J].
Choi, Hyungsam ;
Chung, Im Sik ;
Hong, Kipyo ;
Park, Chan Eon ;
Kim, Sang Youl .
POLYMER, 2008, 49 (11) :2644-2649
[2]   Oligomers and polymers containing phenylethynyl groups [J].
Connell, JW ;
Smith, JG ;
Hergenrother, PM .
JOURNAL OF MACROMOLECULAR SCIENCE-REVIEWS IN MACROMOLECULAR CHEMISTRY AND PHYSICS, 2000, C40 (2-3) :207-230
[3]  
Fang XM, 1998, J POLYM SCI POL CHEM, V36, P461, DOI 10.1002/(SICI)1099-0518(199802)36:3<461::AID-POLA10>3.3.CO
[4]  
2-L
[5]   STRUCTURE AND VISCOELASTIC PROPERTIES OF EPOXY-RESINS PREPARED FROM 4-NUCLEI NOVOLACS [J].
HASEGAWA, K ;
FUKUDA, A ;
TONOGAI, S .
JOURNAL OF APPLIED POLYMER SCIENCE, 1989, 37 (12) :3423-3435
[6]   The use, design, synthesis, and properties of high performance/high temperature polymers: an overview [J].
Hergenrother, PM .
HIGH PERFORMANCE POLYMERS, 2003, 15 (01) :3-45
[7]   Investigation of the thermal curing chemistry of the phenylethynyl group using a model aryl ether imide [J].
Holland, TV ;
Glass, TE ;
McGrath, JE .
POLYMER, 2000, 41 (13) :4965-4990
[8]  
Ishida Y, 2007, 16 INT C COMP MAT KY, Vp4
[9]   Chemical imidization study by spectroscopic techniques. 1. Model amic acids [J].
Kailani, MH ;
Sung, CSP .
MACROMOLECULES, 1998, 31 (17) :5771-5778
[10]  
KAMON T, 1973, KOBUNSHI KAGAKU, V30, P279, DOI 10.1295/koron1944.30.279