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首页> 外文期刊>Polymers for advanced technologies >Synthesis and characterization of poly(L-lactide-co-ε-caprolactone) copolymers: influence of sequential monomer addition on chain microstructure
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Synthesis and characterization of poly(L-lactide-co-ε-caprolactone) copolymers: influence of sequential monomer addition on chain microstructure

机译:聚(L-丙交酯-共-ε-己内酯)共聚物的合成与表征:单体顺序添加对链微结构的影响

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A series of copolymers with various compositions were synthesized by one-step and two-step bulk ring-opening polymerizations of L-lactide (LA) and ε-caprolactone (CL) using stannous octoate [Sn(Oct){sub}2] and 1-hexanol as the initiating system. For the sequential two-step polymerization, a poly(ε-caprolactone) (PCL) prepolymer was polymerized first to a percent conversion of approximately 70% and LA then added in order to produce a copolymer with a chain microstructure different from that obtained from the corresponding one-step reaction. The resulting copolymers were characterized using a combination of nuclear magnetic resonance spectroscopy (1{sup left}H- and 13{sup left}C-NMR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and gel permeation chromatography (GPC). The average sequence lengths of the lactidyl ((l{sub}(LL)){sup}e) and caproyl ((l{sub}cap){sup}e) units, the degree of randomness (R) and the transesterification coefficient (T(II)) were calculated from the 13{sup left}C-NMR spectra. The appearance of a signal due to CapLCap sequences was directly attributable to transesterification of lactidyl (LL) units. It was found that both (l{sub}(LL)){sup}e and (l{sub}(cap)){sup}e values from the two-step syntheses were significantly longer than from the corresponding one-step syntheses, leading to different semi-crystalline morphologies and chain microstructures. The copolymers all showed at least some blocky chain structure as a result of the significant difference in monomer reactivity (LA > CL) between LA and CL. Thermal properties including stability depended on both composition and chain microstructure which could be controlled by the method of synthesis. From their DSC curves, the two-step copolymers were seen to be semi-crystalline whereas the one-step copolymers were mainly amorphous. A more blocky microstructure, as obtained from the two-step method, appeared to result in a lower thermal stability.
机译:使用辛酸亚锡[Sn(Oct){sub} 2]通过L-丙交酯(LA)和ε-己内酯(CL)的一步和两步本体开环聚合反应,合成了一系列具有不同组成的共聚物。以1-己醇为引发体系。对于顺序的两步聚合,首先将聚(ε-己内酯)(PCL)预聚物聚合至约70%的转化率,然后加入LA,以生产链微结构不同于由链烯结构得到的共聚物。相应的一步反应。使用核磁共振波谱法(1 {H}左上和13 C C-NMR),差示扫描量热法(DSC),热重分析(TGA)和凝胶渗透色谱法(GPC)对所得共聚物进行表征。 )。乳酸基((l {sub}(LL)){sup} e)和己酰基((l {sub} cap){sup} e)单元的平均序列长度,随机度(R)和酯交换系数(T(II))是根据13 C-NMR谱计算的。由于CapLCap序列引起的信号出现直接归因于丙二酰基(LL)单元的酯交换反应。发现两步合成的(l {sub}(LL)){sup} e和(l {sub}(cap)){sup} e值都明显长于相应的一步合成导致不同的半结晶形态和链微结构。由于LA和CL之间单体反应性的显着差异(LA> CL),所有共聚物均显示出至少一些嵌段链结构。包括稳定性在内的热性能取决于组成和链微结构,这可以通过合成方法来控制。从它们的DSC曲线可以看出,两步共聚物是半结晶的,而一步共聚物主要是无定形的。由两步法获得的更块状的微观结构似乎导致较低的热稳定性。

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