胶束催化肉桂油水解制备苯甲醛

用微量量热法研究了十二烷基硫酸钠(SDS)和十六烷基三甲基溴化铵(CTAB)胶束对天然肉桂油碱性水解的催化作用,并考察了反应温度、时间、pH对该水解反应的影响。实验室实验及工厂放大实验结果表明,当反应温度为368-375 K、选择碳酸钠和三乙醇胺为混合碱调节pH=10、m(肉桂醛)∶m(水)=1∶4、c(CTAB)=2.03×10-3mol/L、反应时间14 h时,苯甲醛得率最高达61%。     

基于灰度共生矩阵和支持向量机的气液两相流流型识别

根据灰度共生矩阵具有较好的纹理表达能力的特性，提出了一种基于图像灰度共生矩阵和支持向量机相结合的气液两相流流型识别的新方法。该方法利用高速摄影系统获取水平管道内气液两相流的流动图像，经过图像处理后，提取图像灰度共生矩阵的纹理特征，进而建立流型图像的灰度共生矩阵纹理特征向量，并以此特征向量作为流型样本对支持向量机进行训练，实现了对流动图像的流型智能化识别。实验结果表明，支持向量机能够快速准确地识别水平管道内的7种典型流型，整体识别率达到100%，每幅流型图像的判别时间约为1.7 s，为流型在线识别提供一种新方法。     

PVC微孔塑料的研究进展

阐述化学发泡剂、物理发泡剂和添加剂对PVC微孔发泡的影响,综述了PVC微孔发泡成型方法的研究进展,包括间歇成型法、连续挤出成型法和电磁动态挤出成型法。将振动力场引入到微孔发泡过程为PVC微孔塑料连续挤出成型提供了新的思路和研究方向。     

Direct partial oxidation of methane over ZSM-5 catalyst: effects of additives

Previously, it was reported that the direct partial oxidation (DPO) of CH₄ with O₂ over HZSM-5 catalysts produces C₅₊ hydrocarbon liquids when the feed contains a propane or propene additive. This work studies additive effects on C₅₊ production in this system by processing a CH₄/C₃H₈ feed with subsequent removal of the C₃ additive and by processing natural gas feed. Results show C₅₊ production is maintained at constant yields for HZSM-5 catalysts having different zeolitic Al contents after removal of the C₃ additive. Mechanistic implications are discussed. Natural gas DPO consistently produced C₅₊ liquids due to the presence of C₂₊ components in the feed. While C₅₊ yields from natural gas DPO are higher than those observed for CH₄/C₃ feeds, increasing feed O₂ concentration, and thus conversion, deleteriously affected C₅₊ selectivity.     

Experimental studies on extrudate swell behavior of PS and LLDPE melts in single and dual capillary dies

Extrudate swell behavior of polystyrene (PS) and linear low‐density polyethylene (LLDPE) melts was investigated using a constant shear rate capillary rheometer. Two capillary dies with different design configurations were used, one being a single flow channel and the other being a dual flow channel. A number of extrudate swell related parameters were examined, and used to explain the discrepancies in the extrudate swell results obtained from the single and dual flow channel dies, the parameters including output rate and output rate ratio, power law index, wall shear rate, wall shear stress, melt residence time, pressure drop induced temperature rise, flow channel position relative to the barrel centerline, and the flow patterns. It was found in this work that the power law index (n value) was the main parameter to determine the output rate ratio and the extrudate swell between the large and small holes for the dual flow channel die: the greater the n value the lower the output rate ratio and thus decreased extrudate swell ratio. The differences in the extrudate swell ratio and flow properties for PS and LLDPE melts resulted from the output rate ratio and the molecular chain structure, respectively. The extrudate swell was observed to increase with wall shear rate. The discrepancies in the extrudate swell results from single and dual dies for a given shear rate were caused by differences in the flow patterns in the barrel and die, and the change in the melt velocities flowing from the barrel and in the die to the die exit. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1713–1722, 2003     

Studies on blends of natural rubber and ethylene propylene diene rubber modified with phosphorylated cardanol prepolymer: Processability,physico‐mechanical properties,and morphology

The melt processability and physico‐mechanical properties of blends of natural rubber (NR) and ethylene propylene diene rubber (EPDM) containing different dosages (0–10 phr) of phosphorylated cardanol prepolymer (PCP) were studied in unfilled and china‐clay‐filled mixes. The plasticizing effect of PCP in the blends was evidenced by progressive reduction in power consumption of the mixing and activation energy for melt flow with an increase in the dosage of PCP. The PCP‐modified blend vulcanizates showed higher tensile properties and tear strength despite a decrease in the chemical crosslink density (CLD) index. This is presumably due to the formation of a crosslinked network structure of PCP with the rubbers and improved dispersion of the filler particles in the rubber matrix, as evidenced by scanning electron microscopy (SEM) and atomic force microscopy (AFM). Thermogravimetric analysis showed an increase in thermal stability of the blend vulcanizate in presence of 5 phr of PCP. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5123–5130, 2006     

旋转注射式反应注射成型技术混合方式剖析

为了克服反应注射成型技术混合方式存在的缺点，新近出现了一种旋转注射式－ＲＩＭ技术。该技术采用低速旋转注射剪切层流混合方式，具有能耗低，混合效果好，应用广泛等特点，是一种很有应用潜力的新技术，文内对该技术的混合方式进行了简要剖析。     

水合物降压分解的实验及数值模拟

在天然气水合物一维分解模拟系统上进行模拟多孔介质中水合物降压分解的实验。在考虑天然气水合物分解动力学机理以及流体渗流模型的基础上;建立天然气水合物降压分解的数学模型。利用模型对降压实验进行拟合;获得了多孔介质内水合物分解本征速度常数数量级为10 mol·m^-2·Pa^-1·s^-1;比文献中测定的纯水中水合物分解本征速度常数低3个数量级。对模型进行了参数分析;发现对于实验室规模的一维系统;分解动力学过程控制整个分解过程;而对于现场规模的水合物藏;整个开采过程受水合物藏流动特性的控制;而受水合物分解过程的影响较小。     

Ionic elastomer blends of zinc salts of maleated natural rubber and carboxylated nitrile rubber: Effect of grafted maleic anhydride

Zinc neutralized maleated natural rubbers (Zn‐MNR) were prepared by solution grafting and neutralization with zinc acetate in one‐step. It was later used for blending with carboxylated nitrile rubber (XNBR) in the composition of 50/50 parts by weight. The effect of grafted anhydride content (1.2, 1.6, 2.0, and 2.5% wt of NR) on the tensile properties of ionic rubber blends (Zn‐MNR/XNBR) was investigated. The tensile strength of the ionic blends was found to be greater than those of pure rubbers. The modulus, tensile, and tear strength of the blends dramatically increased with increasing levels of grafted anhydride. The ionic rubber blends also possessed superior physical properties compared to those of the corresponding nonionic rubber blends (MNR/XNBR). Dynamic mechanical thermal analysis and scanning electron microscopic studies were performed to verify the process of mixing. Fourier transform infrared spectroscopic studies were carried out to characterize the nature of specific intermolecular interactions between Zn‐MNR and XNBR chain segments. The results indicated that the ion‐ion (Zn⁺ ‐COO^?) interactions between Zn‐MNR and XNBR are formed at the interface, which provides the mean of compatibilization in the ionic rubber blends. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Mullite for Structural, Electronic, and Optical Applications

Mullite (3Al₂O₃·2SiO₂) is becoming increasingly important in electronic, optical, and high-temperature structural applications. This paper reviews the current state of mullite-related research at a fundamental level, within the framework of phase equilibria, crystal structure, synthesis, processing, and properties. Phase equilibria are discussed in terms of the problems associated with the nucleation kinetics of mullite and the large variations observed in the solid-solution range. The incongruent melting behavior of mullite is now widely accepted. Large variations in the solid solubility from 58 to 76 mol% alumina are related to the ordering/disordering of oxygen vacancies and are strongly coupled with the method of synthesis used to form mullite. Similarly, reaction sequences which lead to the formation of mullite upon heating depend on the spatial scale at which the components are mixed. Mixing at the atomic level is useful for low-temperature (<1000°C) synthesis of mullite but not for low-temperature sintering. In contrast, precursors that are segregated are better suited for low-temperature (1250° to 1500°C) densification through viscous deformation. Flexural strength and creep resistance at elevated temperatures are significantly affected by the presence of glassy boundary inclusions; in the absence of glassy inclusions, polycrystalline mullite retains >90% of its room-temperature strength to 1500°C and displays very high creep resistance. Because of its low dielectric constant, mullite has now emerged as a substrate material in high-performance packaging applications. Interest in optical applications mainly centers on its applicability as a window material within the mid-infrared range.