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Synthesis and characterization of novel soluble poly(ether ketone sulfone)s with pendant polychloro groups

机译:新型含侧链多氯基的可溶性聚醚酮砜的合成与表征

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A novel monomer of tetrachloroterephthaloyl chloride (TCTPC) was prepared by the chlorination of terephthaloyl chloride catalyzed by ferric chloride at 175-180 degrees C for 10 h and confirmed by FTIR, MS, and elemental analysis. Five new polychloro substituted poly (aryl ether ketone sulfone)s (PEKSs) with inherent viscosities of 0.68-0.75 dL/g have been prepared from 4,4'-diphenoxydiphenylsulfone, 4,4-bis(2-methylphenoxy) diphenylsulfone, 4,4-bis(3-methylphenoxy)diphenylsulfone, 4,4'-bis(2,6-dimethylphenoxy)diphenylsulfone, and 4,4'-bis(l-naphthoxy)-diphenylsulfone with TCTPC by electrophilic Friedel-Crafts acylation in the presence of DMF with anhydrous AlCl3 as a catalyst in 1,2-dichloroethane, respectively. These polymers having weight-average molecular weight in the range of 76,600-83,900 are all amorphous and show high glass transition temperatures ranging from 213 to 250 degrees C, the 5% weight loss temperature over 450 degrees C, high char yields of 60-67% at 700 degrees C in nitrogen and good solubility in CHCl3 and polar solvents such as DMF, DMSO, and NMP at room temperature. All the polymers formed transparent, strong, and flexible films, with tensile strengths of 85.1-90.8 MPa, Young's moduli of 2.52-3.24 GPa, and elongations at break of 21.227.2%. (c) 2008 Wiley Periodicals, Inc. J Appl Polym Sci 108: 1049-1054, 2008.
机译:新型四氯对苯二甲酰氯(TCTPC)是通过在175-180℃下氯化三氯化铁催化对苯二甲酰氯的氯化反应10 h制得的,并经FTIR,MS和元素分析证实。由4,4'-二苯氧基二苯砜,4,4-双(2-甲基苯氧基)二苯砜,4,制备了五种新的特性粘度为0.68-0.75 dL / g的多氯取代的聚(芳基醚酮砜)s(PEKSs)。在存在条件下,通过亲电Friedel-Crafts酰化作用将4-双(3-甲基苯氧基)二苯砜,4,4'-双(2,6-二甲基苯氧基)二苯砜和4,4'-双(1-萘氧基)-二苯砜与TCTPC DMF与无水AlCl3作为催化剂分别在1,2-二氯乙烷中的合成。这些重均分子量在76,600-83,900范围内的聚合物都是无定形的,并表现出213至250摄氏度的高玻璃化转变温度,超过450摄氏度的5%失重温度,高炭收率60-67在氮气中于700摄氏度下的溶解度为%,在室温下在CHCl3和极性溶剂(如DMF,DMSO和NMP)中具有良好的溶解性。所有聚合物均形成透明,坚固和柔性的膜,拉伸强度为85.1-90.8 MPa,杨氏模量为2.52-3.24 GPa,断裂伸长率为21.227.2%。 (c)2008 Wiley Periodicals,Inc. J Appl Polym Sci 108:1049-1054,2008。

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