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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Competitive Stereocomplexation, Homocrystallization, and Polymorphic Crystalline Transition in Poly(L-lactic acid)/Poly(D-lactic acid) Racemic Blends: Molecular Weight Effects
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Competitive Stereocomplexation, Homocrystallization, and Polymorphic Crystalline Transition in Poly(L-lactic acid)/Poly(D-lactic acid) Racemic Blends: Molecular Weight Effects

机译:聚(L-乳酸)/聚(D-乳酸)外消旋共混物中的竞争性立体复合,同晶和多晶型转变:分子量效应

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摘要

Competitive crystallization kinetics, polymorphic crystalline structure, and transition of poly(l-lactic acid)/poly(d-lactic acid) (PLLA/PDLA) racemic blends with a wide range of molecular weights (MWs) were symmetrically investigated. Stereocomplex (sc) crystallites are exclusively formed in the low-MW racemic blends. However, stereocomplexation is remarkably depressed, and homocrystallization becomes prevailing with increasing MWs of PLLA and PDLA. Suppressed stereocomplexation in high-MW (HMW) racemic blends is proposed to be due to the low chain diffusion ability and restricted intermolecular crystal nucleation/growth. Equilibrium melting point of sc crystallites first increases and then decreases as MW increases. Crystallinity and relative fraction of sc crystallites in racemic blends enhance with crystallization temperature (T-c), and the sc crystallites are merely formed at Tc > 170 degrees C because of their higher thermodynamic stability. In situ wide-angle X-ray diffraction (WAXD) analysis reveals that the stereocomplexation and homocrystallization are successive rather than completely simultaneous, and the stereocomplexation is preceding homocrystallization in isothermal crystallization of HMW racemic blends. Both initial crystalline structure of homocrystallites (hc) and MW influence the heating-induced hc-to-sc transition of HMW racemic blend drastically; the hc-to-sc transition becomes easier with decreasing T-c and MW. After crystallization at the same temperature, sc crystallites show smaller long period than their hc counterparts.
机译:对称地研究了具有广泛分子量(MWs)的聚(l-乳酸)/聚(d-乳酸)(PLLA / PDLA)外消旋共混物的竞争结晶动力学,多晶型晶体结构和转变。立体复合(sc)微晶仅在低MW外消旋共混物中形成。然而,立体络合显着降低,并且随着PLLA和PDLA MW的增加,均相结晶占主导地位。提出在高分子量(HMW)外消旋共混物中抑制立体复合是由于低链扩散能力和分子间晶体成核/生长受限。随着MW的增加,sc微晶的平衡熔点先升高,然后降低。外消旋共混物中sc晶体的结晶度和相对分数随结晶温度(T-c)的提高而增加,并且由于其较高的热力学稳定性,仅在Tc> 170摄氏度下形成sc晶体。原位广角X射线衍射(WAXD)分析表明,立体配合和均晶是连续的而不是完全同时发生的,并且立体配合在HMW外消旋共混物的等温结晶中先于均结晶。均晶(hc)和MW的初始晶体结构都极大地影响加热诱导的HMW外消旋共混物的hc-sc转变。随着T-c和MW的降低,从hc到sc的过渡变得更加容易。在相同温度下结晶后,sc晶粒的长周期要短于hc结晶。

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