Influence of initial chain conformation on the formation of mesoglobule phase in a dilute heteropolymer solution

We have observed, for the first time, that when the initial chain conformation changed from coil to globule, the association of linear poly(N-vinylcaprolactam-co-sodium acrylate) chains could gradually change from a reaction limited to diffusion limited process, reflected in a change of the fractal dimension of the resultant aggregates from ∼2.5 to ∼1.6. Such an influence of the initial chain conformation has been overlooked in past studies of the formation of the mesoglobule phase in a dilute heteropolymer solution.     

潮州公路两侧土壤铅含量及其分布规律研究

本文采用混合酸（HNO3：HCIO4=4：1）对潮州市区公路（东山路，清洁区）两侧的土壤进行处理，利用萃取分光光度法对土壤中的铅进行了测定，并分析了土壤铅污染程度和分布规律。结果表明：潮州市郊区公路两侧土壤中铅的含量比清洁区高1．25～1．90倍，并随距离增大，土壤铅含量逐渐降低。     

南阳直馏柴油碱洗乳化的原因及对策

分析了南阳石蜡精细化工厂直馏柴油碱洗乳化的原因，介绍了该厂直馏柴油碱洗抗乳化措施，这些措施包括：优化操作参数，加强生产管理，深度碱洗柴油轻组分然后轻、重组分混合出厂。这些措施的综合应用彻底解决了南阳石蜡精细化工厂直馏柴油碱洗乳化的问题，又保证了柴油收率。     

花岗岩残积土-土工格栅界面的后循环剪切行为研究

花岗岩残积土在华南、东南沿海、南岳、新疆等地区广泛分布,前人的研究多集中在结构性及微观特性上,后循环加载、位移演化、土壤密度等因素对筋-土界面的剪切特性及加筋作用效果的影响评估研究较少。从循环试验剪切刚度这一重要参数入手,以加载次数、加载频率值、位移振幅值、土壤重度值为自变量,应用控制变量法,通过设计循环直剪试验,得到加筋花岗岩残积土的剪切应力与剪切位移、垂直位移与剪切位移关系曲线进行观察对比,结果表明:花岗岩残积土土工格栅界面剪切刚度受位移半振幅、土壤干重度影响很大,受加载频率影响很小,循环加载并没有弱化后循环界面剪切强度,剪切位移与位移半振幅呈负相关关系。     

1-苯基-3-甲基-4-咔唑-N-丁基-4-苯甲酰基呲唑啉-5-酮的合成及其光谱研究

在苯和50％NaOH介质中，80℃时1，4-二溴丁烷与咔唑(CZ)反应，生成N-溴丁基咔唑(BCZ)。在丙酮和K2CO2介质中，50℃时N-溴丁基咔唑与1-苯基-3-甲基-4-苯甲酰基吡唑啉-5-酮(PMBP)反应，生成1-苯基-3-甲基-4-咔唑-N-丁基-4-苯甲酰基吡唑啉-5-酮(PMCBP)，详细研究了CZ，BCZ，PMBP和PMCBP的UV和IR光谱．在氯仿中PMCBP对Nd(Ⅲ)的萃取率是PMBP的2．3倍，PMBP-Nd(Ⅲ)配合物无荧光，但PMCBP-Nd(Ⅲ)配合物有很强的荧光，说明PM-CBP是Nd(Ⅲ)的优良荧光试剂。     

Electrical conductivity of polyblends of poly(1,4-phenylene vinylene) and poly(2,5-dimethoxy-1,4-phenylene vinylene)

Summary A series of polyblends of poly(1,4-phenylene vinylene), PPV, and poly(2,5-dimethoxy-1,4-phenylene vinylene), PDMPV, were prepared in film form from precursor polyblends of the respective sulfonium salt polymers, which were separately prepared from the respectivebis(sulfonium salt) monomers. The blend films were doped with I₂ at room temperature to obtain a wide range of electrical conductivities (10^–2 to 10²Scm^–1) depending on the blend composition. The higher the content of PDMPV in the blends the higher was the conductivity.     

Comparison of relative viscosity measurement of polyvinylpyrrolidone in water by glass capillary viscometer and differential dual‐capillary viscometer

The relative viscosity (RV) of polyvinylpyrrolidone (PVP) with different molecular weights was measured with a glass capillary viscometer and with a differential dual‐capillary viscometer in water at different concentrations. For the differential dual‐capillary viscometer, RV increases with a decreasing flow rate, especially for high molecular weight PVP at a 1% concentration. A good agreement in the RV between the two methods can be obtained for PVP with different molecular weights and at various concentrations if an appropriate flow rate is selected for the differential dual‐capillary viscometer. Special precaution is needed when using the differential dual‐capillary viscometer to measure the viscosity of a pure solvent. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1312–1315, 2002     

Preparation and properties of heterocyclically conjugated poly(3‐hexylthiophene)–clay nanocomposite materials

A series of heterocyclically conjugated polymer–clay nanocomposite (PCN) materials that consisted of organic poly(3‐hexylthiophene) (P3HT) and inorganic montmorillonite (MMT) clay platelets were prepared by in situ oxidative polymerization with FeCl₃ as an oxidant. The as‐synthesized PCN materials were characterized by Fourier transform infrared (FTIR) spectroscopy, wide‐angle powder X‐ray diffraction (WAXRD), and transmission electron microscopy (TEM). The effects of the material composition on the anticorrosion, gas barrier, thermal stability, flammability, mechanical strength, and electrical conductivity properties of the P3HT and PCN materials were studied by electrochemical corrosion measurements, gas‐permeability analysis (GPA), thermogrametric analysis (TGA), limiting oxygen index (LOI) measurements, dynamic mechanical analysis (DMA), and a four‐point probe technique, respectively. The molecular weights of extracted and bulk P3HT were determined by gel permeation chromatography (GPC) with THF as an eluant. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3438–3446, 2004     

Adsorption and desorption kinetics of hydrocarbons in FCC catalysts studied using a tapered element oscillating microbalance (TEOM). Part 2: numerical simulations

The factors affecting the adsorption and desorption kinetics in a TEOM are reviewed in detail with particular attention given to the assumptions required to obtain physical transport parameters from the data. Two models are presented to simulate TEOM adsorption data in the case that concentration differences down the catalyst bed can be neglected, as is appropriate when the amount of catalyst used is small, the carrier gas flowrate is large, and/or the adsorbate partial pressure is low. In the first model, the effective diffusion coefficient, D_e, is taken to be constant. In the second model, the effective diffusion coefficient is assumed to obey the Darken equation, D_e=D₀/(1−θ). The TEOM results obtained on n-hexane, n heptane, n-octane, toluene and p-xylene on a commercial FCC catalyst and on pure rare-earth exchanged zeolite Y under non-reacting conditions (373-) are analysed in detail. It is found that intracrystalline diffusion is not the limiting factor affecting the overall rates of adsorption and desorption for the systems studied. Instead, it is the transport of molecules between the adsorbed and vapour phases at the edge of zeolite crystallites that is the limiting transport step affecting the overall kinetics. For the FCC catalyst, the limiting step is the transport of molecules at the zeolite-matrix interface rather than, say, the matrix-vapour interface. Local rate constants for the desorption of the hydrocarbons at the rate-controlling interface have been obtained.     

Damping of vinyl acetate–n‐butyl acrylate copolymers

A photopolymerization process at room temperature was devised to copolymerize vinyl acetate (VAc) and n‐butyl acrylate (BA) mainly to prepare rubber‐like damping sheet bearing pressure‐sensitive adhesive property in this study. The investigations using both the differential scanning calorimeter and rheometric dynamic analysis show the existence of two glass transition temperatures for each copolymer. The scanning electron microscopic pictures reveal that the degree of microphase separation increases with increasing annealing time at 70°C. It was suggested that the rubbery domain (formed by the PBA blocks) disperses in the glassy domain (constituted by the PVAc blocks), making an effective damping entity. Excellent damping was observed for the copolymer samples, with the tanδ peak values as high as 1.76–1.80 at a certain temperature range and with tanδ> 0.3 at quite wide temperature ranges. In addition, the copolymers containing more VAc tend to have the higher damping. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1396–1403, 2004