In situ miniemulsion polymerization of water-borne polyurethanes(Ⅰ)Competition of polyaddition with hydrolysis of isocyanate
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In situ miniemulsion polymerization of water-borne polyurethanes(Ⅰ)Competition of polyaddition with hydrolysis of isocyanate
CIESC JournalIssue 2, Pages: 490-495(2009)
作者机构:
浙江大学联合化学反应工程研究所
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Online First:05 February 2009,
Published:05 February 2009
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ZHAN Xiaoli, SHI Ying, ZHANG Qinghua, et al. In situ miniemulsion polymerization of water-borne polyurethanes(Ⅰ)Competition of polyaddition with hydrolysis of isocyanate[J]. CIESC Journal, 2009, (2): 490-495.
DOI:
ZHAN Xiaoli, SHI Ying, ZHANG Qinghua, et al. In situ miniemulsion polymerization of water-borne polyurethanes(Ⅰ)Competition of polyaddition with hydrolysis of isocyanate[J]. CIESC Journal, 2009, (2): 490-495.DOI:
In situ miniemulsion polymerization of water-borne polyurethanes(Ⅰ)Competition of polyaddition with hydrolysis of isocyanate
The polyaddition of isophorone diisocyanate (IPDI) with hydrophobic diol was performed in miniemulsion to obtain water-borne polyurethane.The polymer structure was characterized with FTIR to determine the concentration ratio of urethane to urea group.The effects of hydrophobic diol
vinyl monomers
and such experiment parameters
as temperature
catalyst and surfactant on the competition of the main reaction (polyaddition of isocyanate- hydroxyl) with the side reaction (hydrolysis of isocyanate) were studied.Based on the experimental results
the physical model of the competition was established.It was found that the high reactivity of diol and the high hydrophilicity of vinyl monomer could favor the polyaddition.It was also shown that the hydrolysis could be restrained by decreasing surfactant concentration and decreasing temperature and the amount of catalyst.However
the hydrolysis could be restrained by increasing the surfactant concentration when polydimethyl siloxane (PDMS) took part in polymerization.