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高聚物非等温结晶动力学 总被引:2,自引:0,他引:2
由于等温DSC法测定结晶动力学参数在实验上存在着一定的局限性,这些缺点可通过非等温DSC法来克服。本文基于上述观点介绍了高聚物非等温结晶动力学的理论和实验方法,并对影响动力学过程的一些因素进行了讨论,对非等温结晶动力学的最新情况及发展倾向,应用情况作了介绍。 相似文献
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固相缩聚PET等温结晶动力学 总被引:3,自引:1,他引:3
高聚物等温结晶动力学方面的研究者甚多,由熔融缩聚制备的不同分子量PET的等温结晶动力学及几种不同缩聚催化体系固相缩聚PET的等温结晶动力学已有报道.本文采用一个修正的Avrami方程对固相缩聚PET样品进行系统的等温结晶动力学研究. 相似文献
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尼龙1010非等温结晶动力学与机理研究 总被引:3,自引:0,他引:3
尼龙1010非等温结晶动力学与机理研究朱诚身,王经武,李卓美(郑州大学材料工程系郑州450052)(中山大学高分子研究所广州510275)关键词尼龙1010,非等温结晶动力学,结晶机理,动力学结晶能力尼龙1010的结晶动力学,无论是等温还是非等温,研... 相似文献
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测定高聚物结晶动力学参数的非等温理论和方法 总被引:18,自引:0,他引:18
对测定高聚物结晶动力学参数的非等温结晶理论和等速变温DSC方法进行了讨论,文中包含了作者在此领域研究工作的最新进展。 相似文献
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测定高聚物动力学结晶能力的非等温DSC方法 总被引:5,自引:0,他引:5
研究了从非等温DSC结晶曲线计算高聚物动力学结晶能力的方法.从高聚物非等温结晶动力学微分方程出发导出了计算高聚物动力学结晶能力的新方程.以含有不同催化剂的聚对苯二甲酸乙二酯为例,对其结晶进行了测试与计算.发现合理地选定最快结晶速率温度是计算动力学结晶能力的关键.本方法所得动力学结晶能力能正确反映高聚物的整体结晶信息 相似文献
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采用示差扫描量热(DSC)与同步辐射小角X射线散射(SR-SAXS)技术分别研究了聚己内酯(PCL)的等温与非等温结晶动力学及等温结晶过程中PCL片层结构的变化. 在等温结晶过程中, Avrami指数n≈3, 表明PCL以异相成核的三维球晶方式生长. 同时计算了折叠链表面自由能等结晶动力学参数. 在非等温结晶的过程中, Avrami指数n≈4, 表明PCL以均相成核的三维球晶方式生长. 同步辐射小角X射线散射数据分析表明, 在等温结晶过程中, 长周期与非晶层的平均厚度随着结晶时间的增加会经历先减小后几乎不变的过程, 而结晶层的平均厚度不随结晶时间变化而变化. 同时随着结晶温度的升高, 长周期、结晶层厚度与非晶层厚度等片层结构参数均增加. 相似文献
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高聚物的非等温结晶动力学——从不同速率的升温或降温DSC曲线解析结晶动力学参数 总被引:2,自引:0,他引:2
根据等温DSC法,测定结晶动力学参数在实验上存在着一定的局限性,结晶太快或太慢都难于获得可靠的结果,这就限定了能测定的温度区间。可见,等温DSC法测定结晶动力学参数具有获得的信息量少,结晶起始点难以确定,费时等缺点。这些缺点可通过等速变温DSC法来克服。然而,通过等速变温DSC法测定结晶动力学参数的方法至今还不完善。例如Ozawa曾基于Evans理论把Avrami方程推广于非等温结晶,从Ozawa方程通过等速变温DSC曲线可得到表征结晶机理的函数Avrami $数。和冷却结晶函数。Ozawa方法的不足是从其冷却结晶函数不能解析出表征结晶速率的参数。 相似文献
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采用差示扫描量热(DSC)法对反式-/顺式-1,4-聚异戊二烯共混体系的等温及非等温结晶动力学进行了研究,分别采用Avrami方程和莫志深法对其动力学参数进行了解析.研究结果表明,在反式-/顺式-1,4-聚异戊二烯共混体系的等温及非等温结晶过程中,顺式-1,4-聚异戊二烯(CPI)组分的存在会降低反式-1,4-聚异戊二烯(TPI)组分的结晶速率;在等温结晶过程中,CPI组分会提高TPI组分自身的结晶度;而非等温结晶过程中,CPI则提高了共混物中β晶型的相对含量. 相似文献
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Secondary crystallization of PEA, occurring during DSC scan and performed after isothermal primary crystallization has been investigated. The high temperature exotherm peak has been attributed to the crystallization of amorphous fraction included between crystallites formed at the primary crystallization. The temperature position of the highest rate of the secondary crystallization depended on the temperature of the isothermal primary crystallization. 相似文献
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Melt, cold isothermal crystallization kinetics, and multiple melting phenomena are investigated by differential scanning calorimetry (DSC) for a flame‐retardant phosphorus containing copolyester. The crystallization kinetics was investigated by the Avrami equation. The Avrami exponent is about 2.6 for melt crystallization and about 2 for cold crystallization. The crystallization activation energy for melt crystallization and for cold crystallization is −64.7 and 145.5, respectively. Three melting endotherms are found in the DSC scan, and they are explained in terms of secondary crystallization, primary crystallization, and recrystallization during the scan. A strong evidence of a two‐stage crystallization mechanism was also observed in the DSC isothermal experiment and X‐ray diffraction. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 2269–2277, 1999 相似文献
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利用等温和非等温方法详细研究了芳香族聚酯──热致型聚合物对,对’-联苯二甲酸二辛酯的结晶相和液晶相形成机理,并计算了相变过程中的表面自由能与温度系数,研究结果表明:从介晶相开始的结晶过程是二维异相成核、三维线性增长的,而从各向同性液相开始的液晶相形成过程则是二维异相成核二维线性增长的.对两个晶化过程的表面自由能的研究表明,该聚合物液晶相形成过程的相转变表面自由能比结晶过程小得多,预示了它将具有更大的晶化速率.研究还发现,该聚合物的液晶相形成过程具有比结晶过程大得多的温度敏感性. 相似文献
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An oxyethylene/oxybutylene block copolymer with asymmetric volume fraction (E115B103) was blended with oxybutylene homopolymer (Bh) at different volume fractions of the block (φE). Crystallization behavior of the blends was studied and was compared with that of the blends from a symmetric block copolymer (E114B56). It was found that the crystallization temperature of E115B103/B28 blend is lower than that of the blends from symmetric block copolymer. For the blend with φE= 0.30 breakout crystallization with an Avrami exponent n ≈ 3.0 is observed. At φE = 0.22 the blend exhibits a variable crystallization behavior: confined crystallization with n ≈ 1.0 at lower crystallization temperatures but breakout crystallization at high crystallization temperatures. For the blend with φE = 0.14 and sphere morphology confined crystallization occurs at all crystallization temperatures studied. When compared with the blends from symmetric block copolymer, confined crystallization occurs more easily in the E115B103/B28 blends. The SAXS results agree with the isothermal crystallization kinetics. Deformation of the confined crystalline block is observed in the blend with φE = 0.14 and mixed lamellar and cylinder morphologies in the blend with φE = 0.22. 相似文献
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Shoutian Qiu Zhiqiang Su Zhaobin Qiu 《Journal of Thermal Analysis and Calorimetry》2017,129(2):801-808
In this work, the isothermal and nonisothermal crystallization kinetics of three novel biobased poly(ethylene succinate-co-ethylene sebacate) (PESSe) copolymers was systematically investigated with differential scanning calorimetry under different crystallization conditions from the amorphous state. For the isothermal cold crystallization kinetics study, the Avrami equation could well describe the crystallization process of PESSe at various crystallization temperatures. All three PESSe copolymers crystallized through the same crystallization mechanism; moreover, the overall isothermal cold crystallization rate of PESSe decreased with increasing ethylene sebacate (ESe) comonomer content. The nonisothermal cold crystallization kinetics of PESSe was also studied at different heating rates. With increasing ESe content or heating rate, the nonisothermal cold crystallization exotherm of PESSe copolymers shifted to high temperature range. Both the crystallization rate parameter and crystallization rate coefficient of PESSe copolymers decreased with increasing ESe content, indicating that PESSe copolymer with higher ESe content crystallized more slowly than that with lower ESe content. The Ozawa equation was used to analyze the nonisothermal cold crystallization kinetics of PESSe copolymers, which was found to fit the crystallization process very well. 相似文献
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通过受限液体PVT测量技术对等规聚丙烯的结晶行为进行了研究,采用PVT等压测量模式描述了不同压力场下半结晶聚合物的结晶过程.结果表明,随着压力的升高,等规聚丙烯分子链间的相互作用增强,使得等规聚丙烯分子链段更容易排入晶格中,这是结晶温度和结晶速度升高的主要因素.通过对数据拟合,建立了压力对等规聚丙烯结晶过程参数的影响公式.对Jeziorny结晶动力学模型进行改进,并研究了压力对等规聚丙烯结晶动力学的影响,结果发现,当结晶度大于0.08时,结晶动力学拟合曲线呈较好的线性,分析结果可以对结晶过程的变化机理进行合理地预测,在小于200 MPa压力环境下,等规聚丙烯的结晶生长方式仍是球晶生长模式,晶体的生长符合二维片晶生长方式,自由体积的减小是结晶速率加快的主要原因之一. 相似文献
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A nucleation rate function is proposed for use in analyzing the overall crystallization kinetics of polymers. This function allows for the possibility that the nucleation rate varies substantially during the crystallization. This feature is particularly useful in analyzing nonisothermal crystallization, but it can be used to analyze isothermal crystallization as well. The nucleation rate function was used in the derivation of a modified transformation kinetics equation of the Avrami type. The modified Avrami equation was found to be suitable for kinetics analysis for the data obtained from nonisothermal crystallization at rapid cooling rates. Kinetics parameters used to describe nonisothermal crystallization under rapid cooling rates are presented and discussed. These include crystallization induction time, plateau (crystallization) temperature, crystallization half-time, crystallization rate constant, Avrami index, and newly defined quantities called nucleation index, geometric index, and nucleation rate constant. The procedure used to obtain the nucleation rate constant and nucleation index for the nucleation rate function is described and illustrated by application to the analysis of the crystallization kinetics of polypropylene. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1077–1093, 1997 相似文献
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Hyuk-Soo Moon Byung-Kyu Ryoo Jung-Ki Park 《Journal of Polymer Science.Polymer Physics》1994,32(8):1427-1435
This paper describes the nonisothermal crystallization of molten blends of two semicrystalline polymers, polypropylene (PP) and Nylon-6 (N6). A discussion details the effect of the concentration of the compatibilizing agent, maleic anhydride grafted polypropylene (MAH-g-PP), on the crystallization behavior. The crystallization thermograms showed one crystallization peak or two crystallization peaks, which were significantly affected by the presence of MAH-g-PP. The crystallization temperature of N6 levels off down as the concentration of MAH-g-PP increases, whereas that of PP stays at a roughly constant temperature. These blends containing the compatibilizing agent exhibited concurrent crystallization at the crystallization temperature of PP. The crystallization behavior are also studied by optical microscopy under crossed polarizers. © 1994 John Wiley & Sons, Inc. 相似文献
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Zhao-bin Qiu Zhi-shen Mo Ying-ning Yu Hong-fang Zhang Xian-hong Wang Polymer Physics Laboratory Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun China 《高分子科学》2000,(2):129-132
In this paper, the synthesis and crystallization behavior of poly(ether ether ketone ether ketone) (PEEKEK) arereported. PEEKEK was prepared from 4,4'-bis(p-fluorobenzoyl) diphenyl ether (4,4'-FBDE) and hydroquinone along thenucleophilic substitution route. The thermal properties were investigated by using DSC and TGA. The crystallizationbehavior of PEEKEK under several conditions, i.e., crystallization from the molten state (melt crystallization), crystallizationfrom a quenched sample (cold crystallization) and crystallization induced by exposing glassy sample to methylene chloride(solvent-induced crystallization) has also been investigated. The results show that crystallization of PEEKEK could beinduced by the above methods, and no polymorphism was found. The diflierences in the crystallization of PEEKEK inducedby the above methods are seen in their degree of crystallinity. 相似文献