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Architectural Effects of Poly(omega-caprolactone)s on the Crystallization Kinetics

机译:聚己内酯对结晶动力学的影响

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A series of hyperbranched poly(omega-caprolactone)s (HPCLs)with molecular architectural variation,which refers to the different lengths of the linear backbone segments consisting of 5,10,and 20 e-caprolactone monomer units (thereby referred to as HPCL-5,HPCL-10,and HPCL-20,respectively)and the different numbers of branching points,were synthesized without significant variation in the molecular weights,and linear poly(omega-caprolactone)(LPCL)of the same chemical structure and similar molecular weight was used as the linear counterpart to HPCLs for comparison.The specific molecular architectures of these samples were characterized by ~1H NMR end-group analyses.The nonisothermal crystallization exotherms of HPCLs and LPCL were measured by DSC and further analyzed by the modified Avrami method.Regardless of the samples,the Avrami exponents ranged from 2.4 to 3.3,indicating that the nucleation and growth mechanisms of the samples are apparently identical.On the other hand,the crystallization kinetics was found to be fairly affected by the molecular architectures.All the kinetic parameters estimated from DSC exotherms such as the initial slope,Si,and from the modified Avrami analyses such as the corrected rate constant,K_c and crystallization half-time,t_(1/2),indicated that HPCLs with longer linear segments and fewer branches showed the faster crystallization,whereas LPCL exhibited intermediate crystallization rate between HPCL-10 and HPCL-20,i.e.,HPCL-5 < HPCL-10 < LPCL < HPCL-20.The slower crystallization was linked with the frequent presence of heterogeneous branching points,hindering the regular chain packing,in the backbone of HPCLs with shorter linear segments.In addition,the faster crystallization of HPCL-20 compared with LPCL was attributed to the higher cooperative chain mobility in their melt state as evaluated by activation energy of flow.A number of spherulites developed during isothermal process from the melt were observed for all samples by POM,and the radial growth rates of these spherulites were evaluated to correspond well with the results of Si,K_c,and t_(1/2)from the nonisothermal crystallization analyses.
机译:一系列具有分子结构变异的超支化聚(ω-己内酯)(HPCL),是指由5、10和20个e-己内酯单体单元组成的线性主链段的不同长度(因此称为HPCL-分别合成了5,HPCL-10和HPCL-20以及不同的支化点,分子量没有明显变化,相同化学结构和相似分子的线性聚(ω-己内酯)(LPCL)用重量作为HPCL的线性对应物进行比较。这些样品的特定分子结构通过〜1H NMR端基分析进行表征。通过DSC测量HPCL和LPCL的非等温结晶放热峰,并通过改进的Avrami方法进行进一步分析不论样品如何,Avrami指数的范围从2.4到3.3,这表明样品的成核和生长机理显然是相同的。发现所有动力学参数都受分子结构的影响。从DSC放热估算的所有动力学参数,例如初始斜率Si,以及从改进的Avrami分析估算的动力学参数,例如校正的速率常数K_c和半结晶时间t_ (1/2),表明具有更长线性链段和更少分支的HPCL结晶速度更快,而LPCL表现出介于HPCL-10和HPCL-20之间的中等结晶速率,即HPCL-5

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