PP-R管材料熔融挤出过程MFR控制研究

分析了PP-R（无规共聚聚丙烯）管材料MFR（熔体流动速率）的变化对力学性能的影响，着重通过双螺杆挤出机研究了PP—R管材料熔融挤出过程中影响MFR变化的因素。结果表明，合适的加工工艺控制和优良的抗氧体系是保证PP-R管材料加工过程中MFR稳定的前提。     

回收PET共混物的非等温结晶和熔融行为

采用双螺杆挤出机制备了聚丙烯(PP)/回收聚对苯二甲酸乙二酯(r-PET)、r-PET/马来酸酐接枝PP(PP-g-MAH)和r-PET/甲基丙烯酸缩水甘油酯接枝PP(PP-g-GMA)共混物,并研究了共混物组成、熔融温度与时间以及降温速率对共混物非等温结晶与熔融行为的影响.结果表明,r-PET与PP共混,结晶温度均提高,这与组分间起到异相成核诱导结晶作用有关.r-PET结晶温度随PP-g-MAH用量增加而降低,但受PP-g-GMA用量影响较小;r-PET可提高PP-g-MAH结晶温度,但降低PP-g-GMA结晶温度.熔融温度提高,共混物中PP结晶温度和熔点均降低,r-PET熔融峰形和熔点取决于共混物的熔融温度及界面相互作用.     

Melting and reorganization of poly(ethylene terephthalate) on fast heating (1000 K/s)

For poly(ethylene terephthalate) (PET) and other polymers the origin of the multiple melting peaks observed in differential scanning calorimetry (DSC) curves is still controversially discussed. This is due to the difficulty to investigate the melting of the originally formed crystals exclusively. Recrystallization is a fast process and most experimental techniques applied so far do not allow fast heating in order to prevent recrystallization totally. Developments in thin-film (chip) calorimetry allow scanning rates as high as several thousand Kelvin per second. We utilized a chip calorimeter based on a commercially available vacuum gauge, which is operated under non-adiabatic conditions. The calorimeter was used to study the melting of isothermally crystallized PET. Our results on melting at rates as high as 2700 K/s give clear evidence for the validity of a melting-recrystallization-remelting process for PET at low scanning rates (DSC). At isothermal conditions PET forms crystals, which all melt within a few dozens of K slightly above the isothermal crystallization temperature. There is no evidence for the formation of different populations of crystals with significantly different stability (melting temperatures) under isothermal conditions. Superheating of the crystals is of the order of 10 K at 2700 K/s.     

有机溶剂下盐酸环丙沙星的荧光特性研究

本文在几种有机试剂(乙醇，甲醇，丙酮)条件下，对盐酸环丙沙星产生的荧光特性进行了初步的研究，并初步探讨了有机溶剂下温度对其荧光强度的影响。     

Phase transitions of canola oil sediment

Canola sediment was obtained from an industrial filter cake by solvent extraction. When heated in the differential scanning calorimeter (DSC) (5–100°C), the sediment exhibited a single narrow melting peak at around 74.8°C. No solid-state polymorphic transformation of the material could be detected over this temperature range. The X-ray powder diffraction pattern of canola sediment resembled waxes from other sources with an orthorhombic unit cell. The phase transition behavior of canola sediment in oil was studied by both DSC and polarizing microscopy. With increasing ratio of oil/sediment, a reduction in both melting temperature and transition enthalpy was observed. The shape of the supercooling curve resembled that of the melting curve. The induction time was determined by spectrophotometry and was used to calculate the interfacial free energyσ between sediment and oil; σ=4.71 erg/cm². The effect of temperature and sediment concentration on the clouding time of canola oil was studied; the clouding time was the shortest at 5°C.     

PA6/1212共聚物的性能研究

用差示扫描量热仪对尼龙6/1212(PA6/1212)共聚物的一次、二次熔融行为及结晶行为进行了研究,分析了组成与熔融峰、结晶峰的关系,发现了冷结晶现象;研究了PA1212单体含量为2%~20%的PA6/1212共聚物的力学性能与组成的关系。结果表明,在此组成范围内可制得刚性优良的共聚物,冲击强度也有所改善,当PA1212单体含量为11%时,可得到综合力学性能相对较好的共聚物。     

Influence of composition and molecular mass on the morphology,crystallization and melting behaviour of poly(ethylene oxide)/poly(methyl methacrylate) blends

Results are reported on the influence of composition and molecular mass of components on the isothermal growth rate of spherulites, on the overall kinetic rate constant, on the primary nucleation and on the thermal behaviour of poly(ethylene oxide)/poly(methyl methacrylate) blends. The growth rate of PEO spherulites as well as the observed equilibrium melting temperatures decrease, for a given T_c or ΔT, with the increase of PMMA content.Such observations are interpreted by assuming that the polymers are compatible in the undercooled melt, at least in the range of crystallization temperatures investigated. Thermodynamic quantities such as the surface free energy of folding σ_e and the Flory-Huggins parameter χ₁₂ have been obtained by studying the dependence of the radial growth rate G and of the overall kinetic rate constant K from temperature and composition and the dependence of the equilibrium melting temperature depression ΔT_m upon composition, respectively.     

UHMWPE混炼接枝马来酸酐研究

讨论了超高相对分子质量聚乙烯(UHMWPE)混炼接枝马来酸酐(MAH)过程中，单体MAH用量、引发剂DCP用量、交联抑制剂己内酰胺(CAILA)用量、流动改性剂硬脂酸钙(CaSt2)用量及混炼温度、时间等工艺条件对UHMWPE接枝率和凝胶含量的影响。用红外光谱表征了接枝物的存在。并用滴定分析法和重量分析法测定了接枝物UHMWPE～g～MAH的接枝率和凝胶含量。实验表明，MAH用量为5份、DCP为0．15份、CALA为0．1份、CaSt2为1份时。混炼温度175∽180℃。混炼时间14min时，可得到接枝率0．75％、凝胶含量1．48%的UHMWPE接枝物。     

氯代邻硝基甲苯精制方法的改进

文章讨论了用精馏和熔融结晶粗制氯代邻硝基甲苯的工艺，以及方法的改进。     

Melting aspects of filled compounds in a modular co‐rotating twin screw extruder

In the polymer industry, precompounded materials are widely used. Carefully designed melting experiments were carried out to investigate melting mechanisms in master batched polymer compounds, using an intermeshing co‐rotating twin screw extruder. Calcium carbonate or aluminum powder was master batched with linear low‐density polyethylene (LLDPE). The calcium carbonates, which were used in the compounds, have differences in weight fraction and particle size. The compounds containing filler have higher thermal conductivities and viscosities than neat polyethylene. We observed melting initiation and propagation mechanisms of LLDPE compounds by removal and characterization of polymer compound carcasses in the melting region. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 1990–2012, 2006