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Synthesis and Use of Hydroxyl Telechelic Polybutadienes Grafted by 2-Mercaptoethanol for Polyurethane Resins

机译:2-巯基乙醇接枝聚氨酯树脂的羟基远螯聚丁二烯的合成及应用

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摘要

The grafting of hydroxy telechelic polybutadienes (HTPBD)by 2-mercaptoethanol to saturate 1,2-double bonds which enabled an increase of the -OH functionality of HTPBD is presented.The functionalities of the virgin and grafted HTPBD were characterized both by ~1H-NMR after silylation of the hydroxy end grougps and the consumption of the mercatan was determined by iodine titration.The radical addition of 2-mercaptoethanol to HTPBD was nto complete, which is not acceptable for an industrial application.Hence, the excess of mercaptan was reacted to allyl alcolhol,leading to a new short telechelic diol able to be incorprated by addition of hexamethylene diisocyanate to both these diols.The thermal (glass transition, T_g,and decompositon temperatures),physical (gel time and viscosity),and mechanical (Shore hardness)properties were assessed.It was noted that the higher the hydroxyl functionality.the greater the Shore hardness, the viscosity,and the modulus but the lower the gel time observed with the use of grafted HTPBD in PU resins.Their T_g's were boservced to undergo a slight increase (of 4deg C)in the case of PU prepared fro Poly BD R45 HT in contrast to that noted from Poly BD 20 LM(20deg C),showing a lower phase segregation in that latter case.
机译:提出了2-巯基乙醇将羟基远螯聚丁二烯(HTPBD)接枝到饱和的1,2-双键,从而增加了HTPBD的-OH官能度。初生和接枝的HTPBD的官能度均约为〜1H-通过碘滴定确定甲硅烷基化的羟基末端基团后的NMR和硫醇的消耗量.2-巯基乙醇在HTPBD中的自由基加成反应未完全完成,这在工业应用中是不可接受的,因此,过量的硫醇反应了到烯丙醇中,产生了一种新的短螯合二醇,可以通过将六亚甲基二异氰酸酯添加到这两种二醇中来合成。热(玻璃化转变温度,T_g和分解温度),物理(胶凝时间和粘度)和机械(邵尔评估了羟基的性能,注意到羟基官能度越高,肖氏硬度,粘度和模量越大,但观察到的凝胶时间越短与Poly BD 20 LM(20deg C)相比,在Poly BD R45 HT制备PU的情况下,其T_g值被认为略有增加(4°C),在后一种情况下显示出较低的相偏析。

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