SiO_2微粉中温结合机理的研究

本文研究了ＳｉＯ２微粉、ＳｉＯ２微粉分别与铝酸钙水泥、ｐ－Ａｌ２Ｏ３、ＭｇＯ的混合粉体在３５０℃－１２００℃之间的显微结构。结果表明：ＳｉＯ２微粉及其与其它水化物形成的网状键是高技术浇注料中温强度较高的主要原因。     

CoMoO4负载Mo-V-Cr-Bi氧化物催化剂上甲烷部分氧化的研究

研究了CoMoO4负载Mo-V-Cr-Bi氧化物催化剂上甲烷部分氧化反应,发现反应存在一转折温度,当反应温度低于此温度时,CO是主要产物,而部分氧化产物甲醇的选择性低于20%,而当反应温度高于此温度时,CO的选择性大大降低,而CO2的选择性大大升高,主要产物变为CO2,甲醇的选择性降为0。在O2完全反应的时候,总会有H2生成,特别当反应温度高于转折温度的时候,H2的生成量大大增加。     

注塑产品色差控制技术研究

色差是注塑中最常见缺陷，因其牵涉因素众多，十分难以掌握。本文从实用角度出发，讨论了影响色差主要因素和控制色差的实用技术．为减少色差问题的产生提供了一些好的经验和方法。     

Molecular dynamics and thermal analysis study of anomalous thermodynamic behavior of poly (ether imide)/polycarbonate blends

Molecular dynamics simulation used to study the binary polymer blend of poly (ether imide) (PEI) and polycarbonate (PC) showed that these polymer blends are immiscible. The Flory-Huggins interaction parameter, χ, calculated from simulation reached a minimum value at 80 wt% PEI. The simulation results showed that the concentration dependence of χ was mainly due to electrostatic interaction and van der Waals force. The simulation results were supported by differential scanning calorimetry (DSC) measurements. The DSC measurements showed that there are two distinct glass transition temperatures for all the blends' concentrations. However, at 80wt % PEI, the T_g of PEI-rich phase reached a minimum while that of the PC-rich phase was comparable to its pure form indicating that there is some partial miscibility of PC in the PEI rich phase, but no PEI is incorporated in the PC rich phase. From simulations, the χ versus concentration plot shows the same trend as the experimentally measured glass transition temperature versus concentration plot.     

Effect of agitation in the hydrogenation of castor oil

Castor oil was hydrogenated to evaluate the effect of agitation during hydrogenation. The turbine and propeller impellers were evaluated during hydrogenation of castor oil at various temperatures, pressures, and catalyst concentrations. The effect of impeller position in the agitator at definite oil depth was also evaluated. Hydrogenation of castor oil at 130°C, 2.0 kg/cm² hydrogen gas pressure with 0.5% Ni catalyst for 6 h while using two turbine impellers fitted in an agitator, one close to the reactor bottom and another at a height just below the top oil layer, revolving at 350 rpm, resulted in a product of a iodine value of 4.1, hydroxyl value of 156.4, and slip point of 84°C.     

Retrograde Densification of Calcined and Glass Precursors of Approximate (Bi,Pb)2Sr2Ca2Cu3O10 Stoichiometry

Retrograde densification of pelletized calcines and glasses having an approximate (Bi,Pb)₂Sr₂Ca₂Cu₃O₁₀ starting stoichiometry and sintered at ∼850°C can be described by first-order rate equations. Retrograde densification in the calcine precursors was largely due to the development of open pores, and was approximately proportional to the concentration of the (Bi,Pb)₂Sr₂CaCu₃O₁₀ phase. In the glasses, retrograde densification is mainly caused by porosity accompanying the growth of a needlelike Sr─Ca─Cu─O phase, together with (Bi,Pb)₂Sr₂Ca₂Cu₃O₁₀ and (Bi,Pb)₂Sr₂CaCu₂O₈.     

Synthesis and properties of polystyrene‐b‐poly(ethylene oxide)‐b‐polystyrene triblock copolymers

A series of well‐defined and property‐controlled polystyrene (PS)‐b‐poly(ethylene oxide) (PEO)‐b‐polystyrene (PS) triblock copolymers were synthesized by atom‐transfer radical polymerization, using 2‐bromo‐propionate‐end‐group PEO 2000 as macroinitiatators. The structure of triblock copolymers was confirmed by ¹H‐NMR and GPC. The relationship between some properties and molecular weight of copolymers was studied. It was found that glass‐transition temperature (T_g) of copolymers gradually rose and crystallinity of copolymers regularly dropped when molecular weight of copolymers increased. The copolymers showed to be amphiphilic. Stable emulsions could form in water layer of copolymer–toluene–water system and the emulsifying abilities of copolymers slightly decreased when molecular weight of copolymers increased. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 727–730, 2006     

Fe doping effect on EuTiO3: The magnetic properties and giant magnetocaloric effect

The magnetic properties and magnetocaloric effect for EuTi_1-xFe_xO₃ (x = 0.05, 0.1) compounds are investigated. When a part of Ti⁴⁺ions were substituted by Fe ions, the AFM ordering can be significantly changed to be FM. The EuTi_1-xFe_xO₃ (x = 0.05, 0.1) compounds exhibit a PM to FM transition with decreasing temperature and the Curie temperature is 6 K. Under the field changes of 1 T, and RC are valued to be 10.1 J/kg K and 50.2 J/kg for EuTi_0.95Fe_0.05O₃; 9.6 J/kg K and 47.7 J/kg for EuTi_0.9Fe_0.1O₃, without magnetic and thermal hysteresis. RC is almost twice as much as EuTiO₃ (27 J/kg) as substitution of Fe³⁺ ions for Ti⁴⁺ions, which may be attributed to the magnetic transition (AFM to FM). Therefore, the giant and large RC suggest the EuTi_1-xFe_xO₃ compounds are good materials for magnetic refrigerant.     

Optical properties of high-temperature heat-treated vitrinites

Three vitrinites (C = 80.0, 87.9 wt%, daf and 94.2 wt%, dmmf) have been heat-treated over the temperature range 1000–2400 °C in the presence of argon. The variation of morphological and optical properties of the heat-treated samples is studied systematically using reflected-light microscopy. An optically isotropic, highly reflecting material is formed on the surface of anisotropic particles of two of the vitrinites (C, 80 and 94.2 wt%) during semi-graphitization (1000–1400 °C), which decreases in extent with increasing temperature and is absent at the end of this stage. The development and subsequent disappearance of the isotropic material is probably due to the evolution of volatile matter and subsequent deposition of pyrolytic carbon during semi-graphitization. The continuous increase of bireflectance of these two vitrinite residues, with heat-treatment temperature, indicates progressive improvement in the ordering of the molecular structure. The reflectance of the heat-treated anthracitic vitrinite (C, 94.2 wt%), increases continuously whereas the reflectance of the heat-treated low-rank vitrinite (C, 80 wt% decreases slightly from a maximum during semi-graphitization. The third vitrinite (C, 87.9 wt%) does not develop an optically isotropic highly reflecting material on particle surfaces during semi-graphitization. However, this vitrinite softens during carbonization (25–1000 °C) producing a residue with a mosaictype anisotropic microstructure. The condition of polished surfaces prepared from residues of this vitrinite from the semi-graphitization to crystallization stages (1000–2300 °C) deteriorates, values of bireflectance and reflectance decrease continuously with increasing temperature. This appears to result from a reduction in the surface hardness of particles of this vitrinite residue resulting on transformation from two-dimensional ordering to three-dimensional graphitic ordering.     

半钢子午胎硫化供汽系统改造

在原有供汽系统等压运行条件下，通过合理改造，加装减温减压装置，将原系统分类内胎锅炉房高压供汽系统和老锅炉房低压供汽系统，以满足半钢子午胎对高压蒸汽的需求，达到缩短硫化时间，提高生产能力的目的。