首页> 外文期刊>Journal of Applied Polymer Science >REACTIVE BLENDING OF A FUNCTIONALIZED POLYETHYLENE WITH A SEMIFLEXIBLE LIQUID CRYSTALLINE COPOLYESTER
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REACTIVE BLENDING OF A FUNCTIONALIZED POLYETHYLENE WITH A SEMIFLEXIBLE LIQUID CRYSTALLINE COPOLYESTER

机译:功能化聚乙烯与半柔性液晶共聚物的共混反应

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Reactive blends (50/50 w/w) of a low molar mass polyethylene containing free carboxylic groups (PEox) and a semiflexible liquid crystalline polyester (SBH 1 : 1 : 2, by Eniricerche) have been prepared at 240 degrees C in a Brabender mixer, in the presence of Ti(OBu)(4) catalyst, for different mixing times (15, 60, and 120 min). In order to prove the formation of a PE-g-SBH copolymer, the blends have been fractionated by successive extractions with boiling toluene and xylene. The soluble fractions and the residues have been analyzed by Fourier transform infrared (FTIR) spectroscopy, thermogravimetry (TG and DTG), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM). All analytical procedures concordantly show that PE-g-SBH copolymers with different compositions, arising from differences of either the number of PEox carboxylic groups entering the transesterification or the length of grafted SBH branches, are formed as a result of blending. Depending on the relative content of PE and SBH segments, the copolymers dissolve in the solvents, together with any unreacted PEox, or remain in the residues, together with neat SBH. Qualitative IR analyses and quantitative TG measurements have shown that the amount of copolymers increases strongly with the mixing time. Preliminary SEM observations indicate that the unfractionated products of the reactive blending carried out with long (120 min) mixing times lead to improved interfacial adhesion and phase dispersion when added to PE/SBH blends. (C) 1996 John Wiley & Sons, Inc. [References: 27]
机译:含游离羧基的低摩尔质量聚乙烯(PEox)和半柔性液晶聚酯(SBH 1:1:2,由Eniricerche生产)的反应混合物(50/50 w / w)已在Brabender中于240摄氏度下制备在Ti(OBu)(4)催化剂存在下,进行不同的混合时间(15、60和120分钟)。为了证明形成了PE-g-SBH共聚物,共混物通过用沸腾的甲苯和二甲苯连续萃取进行分馏。已通过傅里叶变换红外(FTIR)光谱,热重分析(TG和DTG),差示扫描量热法(DSC)和扫描电子显微镜(SEM)分析了可溶级分和残留物。所有的分析方法一致地表明,由于共混形成了具有不同组成的PE-g-SBH共聚物,这是由于进入酯交换反应的PEox羧基数或接枝SBH支链长度的差异所致。根据PE和SBH链段的相对含量,共聚物与未反应的PEox一起溶解在溶剂中,或与纯SBH一起残留在残留物中。定性的IR分析和定量的TG测量表明,共聚物的数量随混合时间而大大增加。初步的SEM观察表明,将长时间(120分钟)的混合时间进行的反应性共混物的分馏产物,当添加到PE / SBH共混物中时,会导致界面粘合性和相分散性的改善。 (C)1996 John Wiley&Sons,Inc. [参考:27]

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