Synthesis and characterization of aromatic copolyesters containing siloxane linkages in the polymer backbone

A new series of aromatic copolyesters containing siloxane linkages were prepared by the melt polymerization of bisphenol A (BPA) with eugenol end‐capped siloxane (EuSi), diphenyl terephthalate (DPT), and diphenyl isophthalate (DPI) in varying ratio in the temperature range 220–290°C under reduced pressure in the presence of dibutyl tin dilaurate (DBTL) catalyst. The siloxane copolyesters prepared were characterized by FTIR, ¹H‐NMR spectroscopy, solution viscosity, thermogravimetric analysis, differential scanning calorimetry, and X‐ray diffraction. The effect of incorporation of eugenol end‐capped siloxane was studied on the properties of BPA/DPI/DPT copolyesters. The glass‐transition temperature of copolyester was decreased from 184 to 70°C by incorporation of 20% of eugenol end‐capped siloxane. All copolyesters were found to be soluble in commonly used aprotic polar solvents and had film‐forming properties. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3222–3228, 2006     

铬铁矿液相氧化的热力学分析

液相氧化法生产铬酸盐技术是对传统火法焙烧技术的突破．在600～900K温度范围内对液相氧化法处理铬铁矿的熔盐体系各反应趋势及物相组成的热力学进行了分析研究，对液相氧化法处理铬铁矿各体系的反应自由能变化（△G°R）与温度（T）关系的计算结果表明，铬铁矿中的（Mg,Fe）（CrO2）2在较低温度下与NaOH、O2具有较强的反应趋势，比传统的火法焙烧方法反应温度降低了873K，节约大量能源;铬铁矿中的杂质相在反应温度下进行一系列副反应，生成硅酸盐、铝硅酸盐等新相．     

Side-chain functionalized liquid crystalline polymers and blends, 10: phase behavior and structure of side-chain liquid crystalline ionomers containing ions of d-metals

Novel side-chain liquid crystalline (LC) ionomers containing d-metals Co(II) and Ni(II) were synthesized and characterized. Both families of the ionomers are characterized by the same influence of charged group content in polymer on their phase behavior. The incorporation of 2-3 mol% of metal ions in the nematic polymer matrix leads to the induction of SmA phase and rise in the clearing point. The peculiarity of their phase behavior in comparison with the earlier investigated LC ionomers with alkaline or alkali-earth metals is the full destruction of the mesophase at the concentration of d-metal higher than 12 mol%. This phenomenon was associated with the well-known ability of the transition metal ions to form various complexes that, in the case of LC ionomers, can negatively influence the ordering of the side mesogenic groups. The proposed structure of the LC ionomers is discussed in comparison with the metallomesogenic polymer systems.     

垂直筛板塔流体力学与传质研究状况

对我国在新型垂直筛板塔的流体力学性能 ,诸如塔板干板压降与湿板压降、板孔漏液、塔板过量雾沫夹带、板上帽罩单元的液体提升能力与液体循环程度的研究及其传质性能 ,诸如塔板传质效率模型、塔板空间气相中液体大小与分布、板间空间立体传质作用的研究等进行了综合 ,并予以分析论述 ,从中看出我国对新型垂直筛板塔已进行了较全面深入的研究工作 ,并取得了新进展。     

Study of mass transfer in a vertically moving particle bed electrode

A study was made of the influence of process parameters on the mass-transfer coefficient in a flow-through cell with a cascade of rotating drums partially filled with conductive particles (called the vertically moving particle bed). Copper deposition from an acidic sodium sulphate solution was used as the model reaction. To evaluate the experimental data a macrohomogeneous mathematical model of potential and current density distribution inside the cell was developed. The electrolyte flow distribution between the empty space above the particle bed and through the bed was evaluated. On the basis of these results the following correlation is proposed:

裂解色谱法对共聚物与共混物的鉴定

李文应用裂解色谱法对丙烯酸酯等物质的共聚物与共混物进行了鉴定。     

油水气三相流液体流量调节系统研究与设计

针对油水气三相流研究试验平台液体流量调节范围宽、范围度大的问题,提出采用3条主回路与3条旁通回流调节支路来覆盖所有的流量范围,设计了液相系统原理图及管路布置图,对3条旁通回流调节支路中调节阀的计算流量、计算压差及Kv值进行了计算,并对调节阀的开度及实际可调比进行了验算,结果表明选定的调节阀性能满足油水气三相流研究试验的要求。     

Kinetic study of radical polymerization. II. Solid‐state bulk polymerization of sodium methacrylate by differential scanning calorimetry

The solid‐state radical polymerization of sodium methacrylate was investigated. It was initiated by azobisisobutyronitrile, which was used as a radical initiator. Differential scanning calorimetry (DSC) was used to observe the endothermic and exothermic transitions during the polymerization reaction. Structural studies were performed with the DSC thermograms and Fourier transform infrared and ultraviolet–visible spectra, and all of the results confirmed the progress of the reaction. The obtained data revealed that the polymerization reaction proceeded completely with a 100% conversion. ΔH of this reaction was calculated with various amounts of the initiator, and the peak temperatures were determined at different heating rates. The activation energy (19.7 kcal mol^?1) was also obtained by the Kissinger method for this type of solid polymerization reaction. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1648–1654, 2003     

Structural characterization of reactor blends of polypropylene and ethylene‐propylene rubber

Blends of isotactic polypropylene (PP), ethylene‐propylene rubber copolymer (EPR), and ethylene‐propylene crystalline copolymer (EPC) can be produced through in situ polymerization processes directly in the reactor and blends with different structure and composition can be obtained. In this work we studied the structure of five reactor‐made blends of PP, EPR, and EPC produced by a Ziegler‐Natta catalyst system. The composition of EPR was related to the ratio between ethylene and propylene used in the copolymerization step. The ethylene content in the EPR was in the range of 50–70 mol %. The crystallization behavior of PP and EPC in the blends was influenced by the presence of the rubber, and some specific interactions between the components could be established. By preparative temperature rising elution fractionation (P‐TREF) analysis, the isolation and characterization of crystalline EPC fractions were made. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 2155–2162, 2004     

A water‐developable negative photoresist based on the photocrosslinking of N‐phenylamide groups with reduced environmental impact

A water‐developable negative photoresist based on the photocrosslinking of N‐phenylamide groups was prepared by the copolymerization of 4‐styrenesulfonic acid sodium salts (SSS) with N‐phenylmethacrylamide (copolymer A) or p‐hydroxy‐N‐phenylmethacrylamide (copolymer B), and its properties such as solubility changes, photochemical reaction, and photoresist characteristics were studied. The copolymer containing a relatively higher amount of SSS units was soluble in water. Solubility changes of the copolymers in the various buffer solutions of pH 4 ～ 11 and in water upon irradiation were observed by the measurement of insoluble fraction. The copolymers were soluble in water before irradiation, whereas they became insoluble upon irradiation with the UV light of 254 nm. The photochemical reaction of the copolymer studied by the UV and IR absorption spectroscopies indicated that a photo‐Fries rearrangement was favored for copolymer A, whereas a photocrosslinking reaction was predominate for copolymer B. Resist properties of the copolymers were studied by measurement of the normalized thickness and by development of the micropattern. Negative tone images with a resolution of 1 μm were obtained with these materials that have a sensitivity (D) of ～ 1100 mJ/cm² with an aqueous developing process.© 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1172–1180, 2002