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采用差示扫描量热法(DSC)研究了聚对苯二甲酸丙二醇酯/聚乙烯(PTT/PE)共混体系的非等温结晶动力学,通过热台偏光显微镜(POM)对共混物在等温条件下的结晶形态进行了研究。结果发现:PTT/PE共混体系各样品的结晶峰温度随着冷却速率的提高而下降,而半结晶时间t1/2随着冷却速率的提高而提高;结晶动力学常数Zc随着冷却速率的提高而下降,表明共混体系的结晶速率随着冷却速率的提高而降低;在POM观察的时间范围内各样品的球晶尺寸随着时间的延长而增大,PTT/PE(30/70)共混体系在190℃结晶时,球晶尺寸较大,即球晶生长较快。 相似文献
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采用差示扫描量热法(DSC)研究了聚对苯二甲酸乙二醇酯/聚乙烯(PTT/PE)共混体系的非等温结晶动力学,通过热台偏光显微镜(POM)对共混物在等温条件下的结晶形态进行了研究.结果发现:PTT/PE共混体系各样品的结晶峰温度随着冷却速率的提高而下降,而半结晶时间t1/2随着冷却速率的提高而提高;结晶动力学常数Zc随着冷却速率的提高而下降,表明共混体系的结晶速率随着冷却速率的提高而降低;在POM观察的时间范围内各样品的球晶尺寸随着时间的延长而增大,PTT/PE(30/70)共混体系在190℃结晶时,球晶尺寸较大,即球晶生长较快. 相似文献
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选取均聚物聚对苯二甲酸丙二醇酯(PTT)及PTT/聚对苯二甲酸丁二醇酯(PBT)共混物为研究对象,以偏光显微镜(POM)和X射线衍射(XRD)为研究手段探讨了均聚物PTT的结晶形态,以及结晶温度、共混物的组成、等温结晶时间等因素对PTT/PBT共混物结晶形态和性能的影响。结果表明,PTT形成环带球晶的条件是155℃,PTT/PBT共混物的结晶尺寸由于PBT的引入而变小,在PTT质量分数小于60%以后就不能产生环带球晶;PTT/PBT共混物结晶时是两个组分各自结晶,并且相互竞争,使其生成环带球晶的关键是结晶组分的结晶速率要和非结晶组分之扩散速率相匹配。 相似文献
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聚甲醛/聚氧化乙烯晶/晶共混体系溶液结晶行为 总被引:1,自引:0,他引:1
研究不同组成配比下的聚甲醛(POM)/聚氧化乙烯(PEO)晶/晶共混体系溶液结晶行为和结晶形态.结果表明:POM和PEO溶于其共同溶剂六氟异丙醇(HFIP),溶剂挥发过程中两组分由于分子链的相互作用,形成不完善结晶,POM在DSC升温曲线中出现熔融双峰,高熔点峰与纯POM熔点峰相同,而低熔点峰则随PEO含量增大而降低.PEO熔点随POM含量增大而降低.偏光显微镜测试表明:当体系中PEO质量含量低于40%时,POM球晶明显,其直径随PEO含量增加而增大,PEO形成碎晶;当PEO质量含量在60%到80%之间,POM先结晶形成较小的球晶,PEO后结晶,并可穿越POM球晶继续生长至布满整个视场. 相似文献
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采用偏光显微镜(POM)和差示扫描量热仪(DSC)深入研究了不同配比的聚己酸戊酸共聚酯/聚己二酸乙二醇酯(PHBV/PEA)共混体系在不同结晶温度下的结晶形貌、结晶热力学以及结晶动力学。结果表明:随着结晶温度的升高,PHBV/PEA共混物中PHBV的球晶尺寸和环带间距均有所增大;随着PEA含量的增加,PHBV球晶尺寸增大,结构更加开放,同时共混物中PEA组分受PHBV组分的影响,由原来的大球晶变成了细小的碎晶。此外,同纯PHBV和纯PEA相比,PHBV/PEA共混体系中两种组分的结晶速率均有所降低。 相似文献
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化学组成对PBT/PET共聚酯晶型的影响 总被引:2,自引:0,他引:2
本文用广角X衍射(WAXS)方法研究了PBT/PET共聚酯的化学组成与其晶型结构的关系。结果表明:当PBT链节含量很高时,共聚酯具有接近PBT的两种晶型变体,即卷缩形的α晶型和伸展形的β晶型,在外力的作用下,α晶型向β晶型转变。在应力—应变(S—S)曲线上出现平台区域。除去外力,β晶型能在室温下稳定存在。如果PBT链节含量不占优势,则共聚酯的晶型转变消失,在S—s曲线上只出现一个屈服点。 相似文献
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PET—PBT嵌段共聚酯的结构性能研究 总被引:1,自引:0,他引:1
本文报告了用PSC法和X衍射法等对PET—PBT嵌段共聚酯的结构性能,特别如热性能和结晶性能等的研究结果.实验结果表明,不同PBT组份含量的共聚酯熔点变化呈V字形曲线,在摩尔比为50/50时熔点最低.结晶动力学研究表明,当共聚酯中PBT含量为10%时,结晶速率比常规PET有明显增高.X衍射分析还表明,拉伸对共聚酯结晶的发展有明显的诱导效应,尤其是C轴方向的晶粒尺寸增长. 相似文献
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用 DSC法研究聚对苯二甲酸丁二酯 ( PBT)的结晶动力学 ,分别在 468.15 ,471.15 ,473.15 K的等温条件下进行了 PBT等温结晶实验 ,从 PBT等温结晶曲线和等速降温结晶曲线得到在不同温度条件下的结晶动力学数学模型。运用模型对不同 PBT试样进行分析 ,能较好地解释不同品质 PBT的结晶行为 相似文献
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The compatible nature of a new polyester blend, polybutylene-terephthalate (PBT) and a copolyester of bisphenol-A-neopentyl glycol-terephthalate (CP-350), has been inferred from the single Tg by DSC and dynamic mechanical studies. Compatibility is further confirmed from the progressive melting point depression of PBT, and the increasingly coarse and open spherulitic morphology of the blends as the weight percent of CP-350 increases. At and above 40 weight percent of CP-350, crystallization of PBT is impeded by the presence of high concentrations of CP-350 which results in a low degree of PBT crystallinity (0-8 percent) in such blends. The melt viscosity as a function of blend composition shows a good fit to the Hayashida model. 相似文献
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Cheng‐Fang Ou 《应用聚合物科学杂志》2000,78(13):2363-2368
The POB/PBT copolyesters, designated B28, B46, B64, and B82, were prepared from p‐acetoxybenzoic acid (PAB) and poly(butylene terephthalate) (PBT). The polymeric products obtained were then ground and subjected to solid‐state polymerization under vaccum for 4 h. The melting and crystallization behaviors of these copolyesters haven been studied by differential scanning calorimetry (DSC). In the DSC scan of the POB‐rich composition, the endothermic peak shows obscurely, and enthalpy of fussion becomes small due to the change in the crystalline morphology from isotropic to anisotropic. In general, the melting point of the copolyester is increased by the solid‐state polymerization reaction. Also, thermogravimetric analysis (TGA) were performed with these samples obtained. It was found that the decomposition temperature (Td ) is increased as the POB content is increased. Effects of composition and solid‐state polymerization on the decomposition temperature of copolyesters are also discussed. The crystalline morphology of copolyester was investigated with a Zeiss polarized optical microscope. It was found that the POB/PBT copolyesters with 60 mol % POB was shown to be highly anisotropic. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 2363–2368, 2000 相似文献
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PET-PBT共聚酯的结晶性能 总被引:5,自引:0,他引:5
运用差示扫描量热法(DSC)等分析手段研究了PET-PBT共聚酯的结晶性能。研究表明:共聚酯切片的冷结晶温度(Tc)及熔融结晶温度(Tmc)均随PBT链段的引入及含量的增加而降低,第四单体的加入及其分子质量的改变对Tc及Tmc的影响不同;结晶动力学研究表明共聚酯的最大结晶速率出现的温度与PET相比向低温区转移;X衍射结果表明PBT含量的增加使晶体的晶粒尺寸略有增加。 相似文献
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Summary: Poly(ethylene 2,6‐naphthalate) (PEN) can crystallize either from the glassy state or from the melt state. When crystallized from the glassy state, the sample was quenched from the melt in liquid nitrogen and then annealed at certain crystallization temperatures. When crystallized from the melt state, the sample was cooled to a preset temperature from the melt and then annealed for a certain time. The crystal modifications, morphologies and melting behaviors of PEN were investigated by means of wide‐angle X‐ray diffraction (WAXD), polarized optical microscopy (POM), small‐angle light scattering (SALS) and differential scanning calorimetry (DSC). The results show that an α crystal modification of PEN was obtained when PEN crystallized from the glassy state, whilst a β crystal modification was obtained when PEN crystallized from the melt state at a higher temperature. An hedritic morphology of PEN crystal was obtained with only one melting peak observed in DSC curves when PEN was crystallized at a higher temperature from either the glassy state or the melt state. The α crystal modification could also be obtained when PEN was crystallized at a lower temperature from the melt. Spherulitic or banded spherulitic morphologies of PEN crystals, exhibiting multiple melting peaks in DSC curves, were observed when PEN was crystallized at a lower temperature. The multiple melting behaviors of PEN crystals may be associated with spherulitic structures composed of lamellae of varying thickness.
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对采用熔融纺丝及热牵伸得到的左旋聚乳酸/右旋聚乳酸(PLLA/PDLA)牵伸丝在200℃下进行了不同时间的热处理,并对热处理前后PLLA/PDLA纤维热性能、结晶结构、表面形貌等进行了研究。结果表明:经过热处理后,DSC升温曲线中仅存在sc立构晶熔融峰;当热处理时间为1 min时,即可得到仅含sc立构晶的PLLA/PDLA纤维,随着热处理时间的延长,sc立构晶的熔融峰分峰现象有所减弱,结晶度及晶区取向度均有不同程度的提高,同时晶粒尺寸变小。SEM照片显示,经热处理后PLLA/PDLA纤维表面呈现不规则的突起。 相似文献
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Summary A detailed morphological analysis of the melting process of poly(butylene terephthalate) (PBT) is presented. Investigations were conducted by polarizing optical microscopy, coupling the measurement of depolarized light intensity with examination of morphology of PBT spherulites during their fusion. These analyses allowed to prove that the spherulitic superstructure of PBT developed upon isothermal crystallization from the melt does not vary with temperature until complete melting takes place, despite the large reorganization involved in the fusion process. It is thus shown that the double melting behavior commonly observed in PBT does not arise from the presence of various spherulitic morphologies with different thermal stabilities, and the structural changes caused by the reorganization processes do not involve variations in the spherulitic morphology. The recrystallization of PBT above the apparent melting point was also analyzed, and the role of memory effects of crystalline precursors remaining in the melt was discussed. 相似文献