The deformation behavior of polypropylene film under high strain rates

The relationship between stress and strain for polypropylene film was studied under strain rates from 0.13 to 5.21 s^?1 in order to study the deformation behavior of film under higher strain rates than previous studies. Uniform thickness was obtained in the strain rates from 2.08 to 5.21 s^?1 at 435 K, or from 2.08 to 3.13 s^?1 at 437 K. The temperature rise of film due to the generation of heat from plastic strain influenced the relationship between stress and strain, in particular, at high strain rates and low temperature. Material constants for the constitutive equation of film were determined using the measurements from 2.08 to 5.21 s^?1 at 435 K and from 2.08 to 3.13 s^?1 at 437 K. Film thicknesses during and after transverse direction stretching were successfully predicted by applying the material constants obtained. The authors concluded that the material constants should be determined by applying the stretching conditions, under which there is little or no effect from heat generation and under which film can be stretched uniformly in thickness. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

Thermal conductivity of glass fiber reinforced polypropylene under high pressure

The thermal conductivities of molten polypropylene and its glass fiber composites were measured by the compensating hot wire method. The testing apparatus empolyed was designed and tested in our laboratory. The measurements were carried out with temperatures ranging from 170 to 230°C and pressures from 1 to 2000 kg/cm². The results show that the thermal conductivity increases with increasing pressure and glass fiber content, but is almost independent of temperature. The thermal conductivity data were fitted satisfactorily with a proposed empirical equation for polypropylene and Lewies-Nielsen equation for the composites, respectively.     

Accelerated ageing of polypropylene stabilized by phenolic antioxidants under high oxygen pressure

Polypropylene (PP) samples stabilized by a hindered phenol (Irganox 1010) were submitted to thermal ageing at 80°C in air at atmospheric pressure or in pure oxygen at 5.0 MPa pressure. Both the polymer oxidation and the stabilizer consumption were monitored by Infrared spectrometry and thermal analysis. The stabilizer efficiency, as assessed by the ratio induction time/stabilizer concentration is almost constant at atmospheric pressure even when the stabilizer concentration is higher than its solubility limit in PP (0.4% or 24 × 10^?3 mol L^?1). In contrast, at high pressure, the efficiency decreases almost hyperbolically with the stabilizer concentration when this latter is higher than 6.0 × 10^?3 mol L^?1. The results indicate the existence of a direct phenol‐oxygen reaction negligible at low oxygen pressure but significant at 5.0 MPa pressure. The reality of this reaction has been proved on the basis of a study of the thermal oxidation of a phenol solution in a nonoxidizable solvent. A kinetic model of PP oxidation in which stabilization involves three reactions has been proposed. It simulates correctly the effect of oxygen pressure and stabilizer concentration on carbonyl build‐up and stabilizer consumption. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Heat capacity of polypropylene composite at high pressure and temperature

The heat capacities of isotactic polypropylene and its composite with glass fiber have been measured at high pressure, up to 7 MPa, in the melt state by high pressure differential scanning calorimetry (HPDSC). The values also have been calculated from the data of specific volume (V) measured by dilatometry and thermal conductivity (κ) and thermal diffusivity (α) measured by a compensating hot wire method. The values of the heat capacity measured from HPDSC are consistent with those from the calculation method. The heat capacities of molten polypropylene and its composite increase linearly with temperature at a constant pressure and decrease with pressure at a constant temperature. It was found that the heat capacity of polypropylene is insensitive to molecular weight. The heat capacities of molten polypropylene composites are found to be predicted by an additive rule from the weight fractions of heat capacities of polypropylene and glass fiber.     

Elasticity at large deformations and high strain rates in injection molded polypropylene

The deformation behavior of isotactic polypropylene (PP) as a function of strain rate was investigated at 50°C in uniaxial tension. Injection molded dogbone specimens were tested at high strain rates, ε = 10^?1 – 10² s^?1, and the local deformation in the neck was studied using fast tensile videometry. A strong elastic recoil was observed after fracture in this strain rate range with local elastic strains as high as ?_e = 2.0 – 3.2. The recoil is very fast and takes place within 1 ms. The elastic fraction of the strain at break was found to increase with the local strain rate. The elasticity further depends on strain and temperature. The elastic deformation behavior is part of the known transition from ductile cold drawing behavior to brittle fracture that occurs with strain rate or temperature. The elasticity in PP is thought to be due to a decrease in crystallinity, resulting in a discontinuous crystalline structure comparable to that of thermoplastic elastomers.     

Extension behavior and morphology in polypropylene extended under hydrostatic pressure

The effect of hydrostatic pressure on molecular deformation of polypropylene extended under hydrostatic pressure is investigated by using internal friction measurements, wide angle X-ray diffraction, and polarizing microscopy. A homogeneously transparent straight part is obtained by extending samples in the pressure range from 78 to 128 MPa. The overall mechanical properties of a sample extended under P = 102 MPa is significantly different from that of a sample extended under P = 128 MPa. The difference is related to the magnitude of hydrostatic pressure, the extension ratio, and the extent of transparency. The observed results on the β relaxation in the extended samples is found to be related to the morphological reorganization from a coarse spherulitic to a fine spherulitic structure. The cold-drawn sample at atmospheric pressure has the γ-peak at around °50°C, while the hydrostatically extruded samples and the extended samples have no γ-peak. Consequently, the hydrostatic pressure suppresses the formation of the molecular structure relevant to the γ relaxation.     

The differential cooling curve. A technique for measuring certain fat characteristics

The differential cooling-curve technique consists of a measurement of the difference in the cooling rate of a crystallizing and noncrystallizing fat or oil under specific conditions. The temperature differential between the two samples is measured by thermocouples and is plotted as fractions of a millivolt by a recording potentiometer. The significance of the various peaks encountered in the curves is discussed, and a rapid means of determining trisaturated triglyceride content in modified lard and related fats is presented. The technique is a highly sensitive measurement of the thermal properties of a crystallizing fat, and as such offers an absolute measurement of various degrees of modification of lard. Curves of other fats representing different types of glyceride mixtures are presented.     

A single crystal of polyethylene crystallized under high pressure

A single crystal of polyethylene about 2 μm thick has for the first time been obtained through high pressure crystallization and studied by X-ray diffraction and scanning electron microscopy. A band of a few μm thickness observed on the fractured surface of high pressure crystallized polyethylene is identified as a single crystal at least several tens of μm wide. Furthermore, a bulk composed of several bands stacked approximately parallel gives hexagonal symmetry in an X-ray oscillation photograph, the oscillation axis being parallel to the end surface of the bands. On the basis of these observations, it is concluded that a thick single crystal in the hexagonal phase splits into several bands on the transition from the hexagonal to the orthorhombic phase; 〈110〉 or 〈010〉 of each band in the orthorhombic phase corresponds to one of three possible a-axes in the hexagonal phase.     

不同温度和冷却速率下高温灰渣的结晶行为

采用单热电偶在线观察系统（SHTT）、图像分析程序等研究等温过程中温度和连续冷却过程中冷却速率对于人工配制灰渣结晶行为的影响,通过计算结晶动力学参数分析其析晶机理,并采用FactSage软件预测晶体类型。实验结果表明,等温过程中,温度降低,结晶所需时间先减小后增大,晶体尺寸减小,结晶比例先增大再稳定最后减小,不同温度区间生成晶体类型不同,导致结晶比例在某些温度出现较大的变化。连续冷却过程中,冷却速率增大,初始结晶温度降低,晶体由块状向颗粒状转变,结晶比例先稳定后减小,由于析出的晶体类型不同,结晶比例出现多个稳定区间,达到临界冷却速率后熔渣全部凝固为玻璃态,无晶体析出。由DSC得到的熔渣结晶放热曲线与SHTT得到的结果吻合较好。     

Rheological and crystallisation behaviour of high melt strength polypropylene under gas-loading

The understanding of the rheology and crystallisation under processing conditions like high pressure and gas-loading is crucial in foam-processing. A new method to measure both the rheology and crystallisation is introduced. A pressure cell for a conventional rheometer is firstly used to study the crystallisation process under saturation pressure up to 400 bar.     

纳米聚晶金刚石的高压高温合成

利用自行研制的二级大腔体静高压装置,通过高温超高压下石墨向金刚石的直接转变,合成出了纳米聚晶金刚石块体材料.合成压力约为17GPa,温度约为2300℃.微区X射线衍射分析表明,石墨转变成了立方相的金刚石,扫描电子显微镜及X射线全谱拟合分析显示,合成出来的金刚石晶粒尺寸约16nm.压痕法测得的样品维氏硬度为100GPa以上.     

The use of master curves to describe the simultaneous effect of cooling rate and pressure on polymer crystallization

In a previous work a master‐curve approach was applied to experimental density data to explain isotactic polypropylene (iPP) behaviour under pressure and high cooling rates. Suitable samples were prepared by solidification from the melt under various cooling rate and pressure conditions with the help of a special apparatus based on a modified injection moulding machine. The approach here reported is more general than the case study previously shown, and is suitable to be applied to several materials and for different measures related to crystalline content. The proposed simple model is able to predict successfully the final polymer properties (density, micro‐hardness, crystallinity) by superposition of the effect of cooling rate and the effect of pressure in a wide range of experimental conditions. For this purpose three semi‐crystalline polymers were studied [iPP, polyamide‐6 (PA6) and poly(ethyleneterephthalate) (PET)], which exhibited remarkably different behaviour when crystallized under pressure and high cooling rates Copyright © 2003 Society of Chemical Industry     

Quantification of non-isothermal,multi-phase crystallization of isotactic polypropylene: The influence of cooling rate and pressure

The structure of semi-crystalline polymers is strongly influenced by the conditions applied during processing and is of major importance for the final properties of the product. A method is presented to quantify the effect of thermal and pressure history on the isotropic and quiescent crystallization kinetics of four important structures of polypropylene, i.e. the α-, β-, γ- and mesomorphic phase. The approach is based on nucleation and growth of spherulites during non-isothermal solidification, described by the Schneider rate equations combined with the Komogoroff-Avrami expression for space filling. Using an optimization routine the time-resolved multi-phase structure development is accurately described using crystal phase dependent growth rates and an overall nucleation density, all as function of temperature and pressure. It is shown that the maximum growth rate of the α-, and γ-phase increases with applied pressure, while it decreases for the mesomorphic phase. Addition of β-nucleation agent is interpreted as a secondary nucleation density with a coupled β-phase growth. This complete crystallization kinetics characterization of isotactic polypropylene allows prediction of the multi-phase structure development for a wide range of quiescent processing conditions.     

A structural and spectroscopic investigation of reduced graphene oxide under high pressure

The effect of high pressure on reduced graphene oxide (RGO) has been investigated using X-ray diffraction (XRD) and infrared (IR) absorption spectroscopy. Our XRD measurements show two-step reversible compression in the inter-layer spacing of RGO whereas intra-layer ordering exhibits a high pressure behavior similar to that of graphite up to 20 GPa. The line shape analysis of (1 0 0) peak, representing the intra-layer ordering, suggests presence of local out of plane distortions in RGO in the form of puckered regions which progressively straighten out as a function of pressure. IR measurements show reversible changes in spectroscopic features attributed to remnant functional groups in the inter-layer region. These measurements suggest high stability and recovering ability of RGO under pressure cycling.     

Oxidative degradation of polymers. II. Thermal oxidative degradation of atactic polypropylene in solution under pressure

Atactic polypropylene was oxidized in solution in the presence and absence of radical initiator over the temperature range of 140° to 200°C under oxygen pressure of 3.3 to 12.4 kg/cm², and the effects of metal catalyst and additives on the rate, products, and change in molecular weight distribution were measured. The synergistic effect was observed with cobalt and managanese salts. The deactivation of the metal catalyst was suppressed by the addition of acetic acid and acetic anhydride as solvent. The rate of oxidation increased with increasing temperature, but the decrease in molecular weight was nevertheless not so significant as to give many low-boiling products. However, the production of mixtures of acid, ketone, alcohol, and ester with molecular weights of several hundreds was promising. The refractive index of polypropylene decreased markedly as the oxidation proceeded, and the complications involved in the determination of the change in molecular weight distribution measured by gel permeation chromatography are discussed.     

A new approach for determining the critical cooling rates of nucleation in glass‐forming liquids

Crystallization of a liquid below liquidus temperature is a complex process due to simultaneous nucleation and growth of crystals. Nucleation is the crucial initial step of the crystallization process, and affects the glass‐forming ability, especially when there is a large overlap between nucleation and crystal growth versus temperature curves. From the temperature‐time‐transformation (TTT) diagram, one can estimate the critical cooling rate, , of glass‐formation, however this is time‐consuming. In this paper, we establish a simple approach to determine the using calorimetric and viscometric data. Based on the classical nucleation theory, the correlation between the crystallization onset temperature and cooling rate is described by combining two temperature‐dependent functions. The new approach is applicable to a wide range of glass‐forming systems. This work also gives insight into heterogeneous nucleation and glass formation kinetics.