梯度固化聚氨酯脲中氢键的红外光谱分析

doi:10.3964/j.issn.1000-0593.2008.03.030

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Abstract Hydrogen bondings in polyurethane urea elastomer,which reflect the microphase separation,have an important effect on the properties of the elastomer. The polyurethane urea elastomers,whose degree of microphase separation changed gradually,were prepared in the graded temperature field. Hydrogen bondings in them were investigated by FTIR technology. The discussions about CO,NH,and —O— stretching vibration spectra were given. The percentage of hydrogen bonded carbonyl groups increases with the increase in the curing temperature in the thickness direction,which indicates the increase in the degree of microphase separation in it. The degree of hydrogen bonded ether oxygen atoms exhibits obvious difference in polyurethane urea with different crosslinking degree. It is this difference that leads to a contrast changing trend of the percentage of hydrogen bonded NH in different samples. Three-dimensional hydrogen bonding between urea carbonyl and NH is stronger than the hydrogen bonding between ether oxygen atoms and NH. The stretching vibration of hydrogen bonded ether group is at about 1 076 cm^-1.

Key words：Hydrogen bonding;FTIR;Polyurethane;Gradient;Curing temperature;Microphase separation

Received: 2006-11-20 Accepted: 2007-02-26

ZTFLH:

O657.3

Corresponding Authors: ZHAO Pei-zhong E-mail: zpzgraduate@163.com

Cite this article:

ZHAO Pei-zhong,WEN Qing-zhen,WANG Yuan-sheng, et al. Analysis of Hydrogen Bondings in Polyurethane Urea Cured in Graded Temperature Field by FTIR[J]. SPECTROSCOPY AND SPECTRAL ANALYSIS, 2008, 28(03): 551-554.

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https://www.gpxygpfx.com/EN/10.3964/j.issn.1000-0593.2008.03.030 OR https://www.gpxygpfx.com/EN/Y2008/V28/I03/551

[1] Furukawa M,Mitsuia Y,Fukumarua T,et al. Polymer,2005，46：10817.
[2] Velankar S,Cooper S L. Macromolecules,2000，33(2)：382.
[3] Yilgor I,Yilgor E,Guler I G,et al. Polymer,2006，47：4105.
[4] Chu B,Gao T,Li Y,et al. Macromolecules,1992，25(21)：5724.
[5] Tan H,Guo M,Du R,et al. Polymer，2004，45：1647.
[6] WANG Ying-kang,LI Xuan(王盈康，李玄). Acta Sinca Polymerical(高分子学报)，1989，(5)：513.
[7] GUO Xiao-zhan，WANG Zhu，ZHANG Guo-bao，et al(郭晓战，王著，张国宝，等). Spectroscopy and Spectral Analysis(光谱学与光谱分析)，2001，21(2)：169.
[8] Seymour R W,Estes G M,Cooper S L. Macromolecules，1970，3(5)：579.
[9] Yang W P,CHEN Zhu-sheng，Macosko C W(Yang W P,陈竹生，Macosko C W). Polymer Materials Science and Engineering(高分子材料科学与工程)，1992，8(6)：84.
[10] LUO Ning，WANG De-ning，YING Sheng-kang(罗宁，王得宁，应圣康). Acta Sinca Polymerical(高分子学报)，1996，(4)：423.
[11] LI Zai-feng，ZHANG Tian-lin，XU Chun-ming(李再峰，张田林，徐春明). Spectroscopy and Spectral Analysis(光谱学与光谱分析)，2004，24(19)：1066.
[12] Lee H S，Wang Y K，Hsu S L. Macromolecules，1987，20(9)：2089.
[13] WANG Ying-kang,LI Xuan(王盈康，李玄). Acta Sinca Polymerical(高分子学报)，1989，(3)：322.
[14] Coleman M M，Lee K H，Skrovanek D J,et al. Macromolecules，1986，19(8)：2149.
[15] Paik Sung C S，Smith T W，Sung N H. Macromolecules，1980，13(1)：117.
[16] ZHAO Pei-zhong，HUA Xing-yan，ZHU Jin-hua，et al(赵培仲，花兴艳，朱金华，等). China Elastomerics(弹性体)，2005，15(2)：37.
[17] LUO Ning，WANG De-ning，YING Sheng-kang(罗宁，王得宁，应圣康). Polymer Bulletin(高分子通报)，1998，(3)：73.
[18] LI Zai-feng，XU Chun-ming，YIN Shu-mei，et al(李再峰，徐春明，殷树梅，等). Spectroscopy and Spectral Analysis(光谱学与光谱分析)，2002，22(5)：774.
[19] XIU Yu-ying，LUO Zhong-yu，WANG De-ning，et al(修玉英，罗钟瑜，王得宁，等). Journal of South China University of Technology(Natural Science)(华南理工大学学报·自然科学版)，1997，25(18)：44.
[20] FU Xian-shu，CHENG Fa，LI Hou-ping，et al(付贤树，程发，李厚萍，等). Chemical Industry and Engineering(化学工业与工程)，2005，22(4)：267.
[21] Furukawa M，Hamada Y，Kojio K. Journal of Polymer Science,Part B: Polymer Physics，2003，41：2355.
[22] CHENG Shi-yuan，LI Jian-zong，CHEN Qing-yuan(程时远，李建宗，陈清元). Polymer Bulletin(高分子通报)，1994，(1)：37.