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首页> 外文期刊>Journal of the Korean Chemical Society >Polymerization of Vinyl Monomers Initiated by Cobalt () Chloride
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Polymerization of Vinyl Monomers Initiated by Cobalt () Chloride

机译:氯化钴引发的乙烯基单体的聚合

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The polymerization of methyl methacrylate initiated by cobalt(¥±) chloride in tetrahydrofuran has been studied. The conversion was increased liearly with polymerization time at initial stage of 6?-7% conversion and then the rate of polymerization was slightly reduced, and after that the autoacceleration was observed. The rate of polymerization was increased with the concentration of cobalt(¥±) chloride, but at the concentration of cobalt(¥±) chloride higher than 3.4??10-4 mole/l the rate of polymerization was decreased. The rate of polymerization was dependent on the 1.38 power of the concentration of methyl methacrylate. The effect of the radical inhibitor DPPH was observed and the inhibition time was increased with the concentration of DPPH. The apparent overall activation energy was calculated to be 13.2 kcal/mole. In the copolymerization of methyl methacrylate (M1) and styrene (M2), the monomer reactivity ratio was found to be r1 = 2.35, r2 = 0.78. From the above results. the initiation mechanism of polymerization was discussed and it was considered that the polymerization proceeds mainly via diradical mechaism.
机译:研究了氯化钴(¥±)引发的甲基丙烯酸甲酯在四氢呋喃中的聚合反应。转化率随聚合时间的增加而略有增加,在初始转化率是6′-7%时,然后聚合速率略有降低,此后观察到自加速作用。聚合速率随氯化钴(¥±)的浓度而增加,但当氯化钴(¥±)的浓度高于3.4≤10-4 mol / l时,聚合速率降低。聚合速率取决于甲基丙烯酸甲酯浓度的1.38幂。观察到自由基抑制剂DPPH的作用,并且随着DPPH的浓度增加了抑制时间。表观总活化能经计算为13.2kcal /摩尔。在甲基丙烯酸甲酯(M1)和苯乙烯(M2)的共聚中,发现单体反应性比为r1 = 2.35,r2 = 0.78。从以上结果。讨论了聚合反应的引发机理,认为聚合反应主要是通过双自由基机理进行的。

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