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Copolymerization of Styrene and Pentadecylphenylmethacrylate (PDPMA): Synthesis Characterization Thermomechanical and Adhesion Properties

机译:苯乙烯和甲基丙烯酸十五烷基苯酯(PDPMA)的共聚:合成表征热机械和粘合性能

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摘要

The copolymerization of styrene (St) with a bioderived monomer, pentadecylphenyl methacrylate (PDPMA), via atom transfer radical polymerization (ATRP) was studied in this work. The copolymerization reactivity ratio was calculated using the composition data obtained from H NMR spectroscopy, applying Kelen-Tudos and Finemann-Ross methods. The reactivity ratio of styrene (r = 0.93) and PDPMA (r = 0.05) suggested random copolymerization of the two monomers with alternation. The copolymerization conversion increased with increasing PDPMA concentration of the feed, upto 70 wt % PDPMA, but decreased thereafter. The molecular weight determined by gel permeation chromatography was lower than the theoretical values and the polydispersity increased from 1.32 to 2.19, with increasing PDPMA content in the feed. The influence of styrene content on the glass transition and thermal decomposition behavior of the copolymers was studied by differential scanning calorimetry (DSC) and thermogravimetric analysis, respectively. Morphological characterization by transmission electron microscopy (TEM) revealed a phase separated soft core-hard shell type structure. The complex viscosity and adhesion properties like peel strength and lap shear strength of the copolymer on different substrates increased with increasing styrene content.
机译:在这项工作中,研究了苯乙烯(St)与生物衍生单体甲基丙烯酸十五烷基苯基酯(PDPMA)的原子转移自由基聚合(ATRP)的共聚合。使用得自H NMR光谱的组成数据,使用Kelen-Tudos和Finemann-Ross方法,计算共聚反应率。苯乙烯(r = 0.93)和PDPMA(r = 0.05)的反应性比表明这两种单体交替发生无规共聚。共聚转化率随着进料的PDPMA浓度的增加而增加,最高达到70wt%的PDPMA,但是此后降低。通过凝胶渗透色谱法测定的分子量低于理论值,并且随着进料中PDPMA含量的增加,多分散度从1.32增加至2.19。分别通过差示扫描量热法(DSC)和热重分析法研究了苯乙烯含量对共聚物的玻璃化转变和热分解行为的影响。通过透射电子显微镜(TEM)的形态学表征揭示了相分离的软核-硬壳型结构。共聚物在不同基材上的复数粘度和粘附性(如剥离强度和搭接剪切强度)随苯乙烯含量的增加而增加。

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