首页> 外文期刊>Polymer international >Synthesis and characterization of biodegradable aliphatic-aromatic nanocomposites fabricated using maleic acid-grafted poly[(butylene adipate)-co-terephthalate] and organically modified layered zinc phenylphosphonate
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Synthesis and characterization of biodegradable aliphatic-aromatic nanocomposites fabricated using maleic acid-grafted poly[(butylene adipate)-co-terephthalate] and organically modified layered zinc phenylphosphonate

机译:使用马来酸接枝聚[(丁烯己二酸丁酯) - 对苯二甲酸酯合成的可生物降解脂族芳烃纳米复合材料的合成与表征,有机改性层状磷酸锌磷酸盐

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摘要

A new series of biodegradable aliphatic-aromatic nanocomposites containing maleic acid-grafted poly[(butylene adipate)-co-terephthalate] (g-PBAT) and organically modified layered zinc phenylphosphonate (m-PPZn) were successfully synthesized through transesterification and polycondensation processes with covalent linkages between the polymeric and inorganic materials. Fourier transform infrared and C-13 NMR spectra demonstrate the successful grafting of maleic acid to PBAT. The morphology of g-PBAT/m-PPZn nanocomposites was investigated using wide-angle X-ray diffraction and transmission electron microscopy. Results showed that the stacking layers of m-PPZn were distributed and intercalated into the g-PBAT polymer matrix. The incorporation of m-PPZn into the g-PBAT matrix significantly enhanced the storage modulus at -70 degrees C as compared to that of neat g-PBAT. A reduction in thermal stability was observed for all g-PBAT/m-PPZn systems, which is probably due to the lower thermal stability of m-PPZn. The biodegradation of neat g-PBAT copolymers and g-PBAT/m-PPZn nanocomposites was investigated using lipase from Pseudomonas sp. The degradation rates of neat g-PBAT copolymers decrease in the order g-PBAT-80 > g-PBAT-50 > g-PBAT-20. The faster degradation rate of g-PBAT-80 is a result of the higher content of adipate acid units and the chain flexibility of the polymer backbone. Furthermore, the weight loss increases as the loading of m-PPZn increases, indicating that the presence of m-PPZn improves the degradation of the g-PBAT copolymers. This result might be accounted for by the lower degree of crystallinity for g-PBAT/m-PPZn nanocomposites. (c) 2019 Society of Chemical Industry
机译:通过酯交换和缩聚过程成功地合成了一种新的含马来酸接枝的聚[(丁烯己二酸丁酯)-CO-苯二甲酸酯](G-PBT)和有机改性的层状锌膦酸盐(G-PBZN)的新系列可生物降解的脂族 - 芳香纳米复合材料。聚合物和无机材料之间的共价键。傅里叶变换红外和C-13 NMR光谱证明了马来酸的成功接枝到PBAT。使用宽角X射线衍射和透射电子显微镜研究了G-PBAT / M-PPZN纳米复合材料的形态。结果表明,M-PPZN的堆叠层分布并嵌入到G-PBAT聚合物基质中。与整齐G-PBAT相比,将M-PPZN掺入G-PBAT基质中显着增强了-70℃的储存模量。对于所有G-PBAT / M-PPZN系统,观察到热稳定性的降低,这可能是由于M-PPZN的较低的热稳定性。使用Pseudomonas SP的脂肪酶研究纯G-PBAT共聚物和G-PBAT / M-PPZN纳米复合材料的生物降解。 Neat G-PBAT共聚物的降解率在G-PBAT-80> G-PBAT-50> G-PBAT-20中降低。 G-PBAT-80的更快降解速率是己二酸酸单元含量较高的结果和聚合物主链的链柔性。此外,随着M-PPZN的负载增加,重量损失增加,表明M-PPZN的存在改善了G-PBAT共聚物的劣化。该结果可以通过G-PBAT / M-PPZN纳米复合材料的较低程度的结晶度来计算。 (c)2019年化学工业协会

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