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Free-radical copolymerization of methyl methacrylate with styrene in the presence of 2-mercaptoethanol II. Influence of methyl methacrylate/styrene ratio

机译:在2-巯基乙醇II的存在下,甲基丙烯酸甲酯与苯乙烯的自由基共聚。甲基丙烯酸甲酯/苯乙烯比率的影响

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The free-radical copolymerization of methyl methacrylate (MMA) with styrene (St) in the presence of 2-mercaptoethanol (ME) was investigated in order to obtain omega-hydroxy oligomers with random copolymer-type chains of various compositions and molecular weights. Polymerizations at three different MMA/St molar ratios were carried out, while keeping constant the ME/monomer ratio. Monomer mixtures richer in MMA than in St were employed in order to attempt preparing lower polydispersity oligomers with monomodal molecular weight distribution (MWD). The molecular weights of the resulting oligomers increased with both conversion and MMA fraction in the feed, while polydispersities increased with conversion and decreased with MMA concentration in the initial monomer mixture. For the lower MMA fractions in the monomer feed, bimodal MWDs resulted beyond a certain conversion due to the faster relative consumption of ME than of monomer. Based on the pseudo-kinetic rate constant method, apparent chain transfer constants corresponding to the three different compositions of the monomer feed were estimated. The values obtained were in good agreement with the evolution of molecular weights and poiydispersities with conversion and MMA fraction in the monomer feed. The co-oligomers prepared displayed functionalities around unity, making them suitable for the synthesis of macromonomers. (C) 2002 Elsevier Science Ltd. All rights reserved. [References: 26]
机译:为了获得具有各种组成和分子量的无规共聚物型链的ω-羟基低聚物,研究了在2-巯基乙醇(ME)存在下甲基丙烯酸甲酯(MMA)与苯乙烯(St)的自由基共聚。以三种不同的MMA / St摩尔比进行聚合,同时保持ME /单体比恒定。为了尝试制备具有单峰分子量分布(MWD)的较低的多分散性低聚物,使用了比St中的MMA含量更高的单体混合物。所得低聚物的分子量随进料中的转化率和MMA分数的增加而增加,而多分散度随转化率的增加而增加,并且随着初始单体混合物中MMA浓度的降低而降低。对于单体进料中较低的MMA馏分,由于ME的相对消耗快于单体,因此双峰MWD的转化率超出了一定的转化率。基于拟动力学速率常数方法,估算了对应于单体进料的三种不同组成的表观链转移常数。获得的值与分子量和聚合物分散度随单体进料中的转化率和MMA分数的变化高度一致。制备的共聚低聚物显示出统一的官能度,使其适合于大分子单体的合成。 (C)2002 Elsevier ScienceLtd。保留所有权利。 [参考:26]

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