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首页> 外文期刊>Journal of Applied Polymer Science >Catalyzed Chain Extension of Poly(butylene adipate) and Poly(butylene succinate) with 2,2 '-(1,4-Phenylene)-bis(2-oxazoline)
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Catalyzed Chain Extension of Poly(butylene adipate) and Poly(butylene succinate) with 2,2 '-(1,4-Phenylene)-bis(2-oxazoline)

机译:带有2,2'-(1,4-亚苯基)-双(2-恶唑啉)的聚己二酸丁二酯和琥珀酸丁二酯的催化扩链

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Low-molecular-weight HOOC-terminated poly(butylene adipate) prepolymer (PrePBA) and poly(butylene succinate) prepolymer (PrePBS) were synthesized through melt-condensation polymerization from adipic acid or succinic acid with butanediol. The catalyzed chain extension of these prepolymers was carried out at 180-220 degrees C with 2,2'-(1,4-phenylene)-bis(2-oxazoline) as a chain extender and P-toluenesulfonic acid (p-TSA) as a catalyst. Higher molecular weight polyesters were obtained from the catalyzed chain extension than from the noncatalyzed one. However, an improperly high amount of p-TSA and a high temperature caused branching or a crosslinking reaction. Under optimal conditions, chain-extended poly (butylene adipate) (PBA) with a number-average molecular weight up to 29,600 and poly(butylene succinate) (PBS) with an intrinsic viscosity of 0.82 dL/g were synthesized. The chain-extended polyesters were characterized by IR spectroscopy, H-1-NMR spectroscopy, differential scanning calorimetry (DSC), thermogravimetric analysis, wide-angle X-ray scattering, and tensile testing. DSC, wide-angle X-ray scattering, and thermogravimetric analysis characterization showed that the chain-extended PBA and PBS had lower melting temperatures and crystallinities and slower crystallization rates and were less thermally stable than PrePBA and PrePBS. This deterioration of their properties was not harmful enough to impair their thermal processing properties and should not prevent them from being used as biodegradable thermoplastics. The tensile strength of the chain-extended PBS was about 31.05 MPa.
机译:通过己二酸或丁二酸与丁二醇的熔融缩聚反应合成了低分子量HOOC封端的聚己二酸丁二酯预聚物(PrePBA)和聚丁二酸丁二酯预聚物(PrePBS)。这些预聚物的催化扩链反应是在180-220℃下,以2,2'-(1,4-亚苯基)-双(2-恶唑啉)为增链剂和对甲苯磺酸(p-TSA)进行的作为催化剂。从催化的链增长得到的分子量比未催化的高。但是,p-TSA的量过多和高温导致支化或交联反应。在最佳条件下,合成了数均分子量高达29,600的扩链聚己二酸丁二酯(PBA)和特性粘度为0.82 dL / g的聚丁二酸丁二酯(PBS)。通过IR光谱,H-1-NMR光谱,差示扫描量热法(DSC),热重分析,广角X射线散射和拉伸试验来表征扩链聚酯。 DSC,广角X射线散射和热重分析表征表明,与PrePBA和PrePBS相比,扩链的PBA和PBS具有较低的熔融温度和结晶度以及较慢的结晶速率,并且热稳定性较差。其性能的这种恶化不足以损害其热处理性能,并且不应阻止其用作可生物降解的热塑性塑料。扩链的PBS的拉伸强度为约31.05MPa。

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