PE基聚硅氧烷/改性SiO2超疏水薄膜的构筑

使用十八烷基三甲氧基硅烷(OTMS)对纳米SiO2进行表面疏水改性,将得到的改性纳米SiO2(OTMS-SiO2)添加到有机硅树脂(SI)中,然后采用两步法在聚乙烯(PE)薄膜表面固化制备了复合涂层SI/OTMS-SiO2.通过FTIR、1HNMR、29SiNMR、TGA对OTMS-SiO2及复合涂层进行了表征,采用接触角测量仪、SEM、AFM对复合涂层疏水特性和形貌进行了测试和观察,最后对复合涂层的耐磨性和附着力进行了分析.结果表明,SiO2表面成功引入了OTMS,且OTMS-SiO2均匀附着在硅树脂涂层上,增加了表面粗糙度,得到了PE基固化超疏水复合涂层.当OTMS-SiO2添加量为正己烷质量的8％时,制得的复合涂层的水接触角为154°,滚动角为7°,并具有良好的耐磨性,其附着力可达4A等级.     

沉淀法白炭黑化学指标与胶料物理性能的关系

分析了沉淀法白炭黑BET，CTAB，Ssears比表面，DBP吸油值，平均粒径与粒径分布对胶料物理性能的影响。得出结论：满足轮胎综合力学性能的沉淀法白炭黑应为低BET比表面积，低BET与CTAB比，高BET与Ssears比，适中的DBP吸油值，中值粒径小且易崩解的产品。     

Mode of oleic acid adsorption on rice hull ash cristobalite

Fourier transform infrared spectroscopy was used to investigate the adsorption of oleic acid (OA) onto dry rice hull ash (RHA) silica. Adsorption partially occurred by surface hydrogen bonding of the carboxylic acid. There was also formation of carboxylate ions by reaction of OA with residual potassium oxide. These ions were strongly bound by the ash. Isopropanol inhibited OA adsorption by H-bonding and encouraged desorption of H-bonded OA, but without itself being significantly bound. RHA with 40% moisture also adsorbed a small amount of OA by H-bonding and reacted with OA to form and adsorb carboxylate ions.     

Graft polymerization of vinyl acetate onto silica

The free‐radical graft polymerization of vinyl acetate onto nonporous silica particles was studied experimentally. The grafting procedure consisted of surface activation with vinyltrimethoxysilane, followed by free‐radical graft polymerization of vinyl acetate in ethyl acetate with 2,2′‐azobis(2,4‐dimethylpentanenitrile) initiator. Initial monomer concentration was varied from 10 to 40% by volume and the reaction was spanned from 50 to 70°C. The resulting grafted polymer, which was stable over a wide range of pH levels, consisted of polymer chains that are terminally and covalently bonded to the silica substrate. The experimental polymerization rate order, with respect to monomer concentration, ranged from 1.61 to 2.00, consistent with the kinetic order for the high polymerization regime. The corresponding rate order for polymer grafting varied from 1.24 to 1.43. The polymer graft yield increased with both initial monomer concentration and reaction temperature, and the polymer‐grafted surface became more hydrophobic with increasing polymer graft yield. The present study suggests that a denser grafted polymer phase of shorter chains was created upon increasing temperature. On the other hand, both polymer chain length and polymer graft density increased with initial monomer concentration. Atomic force microscopy–determined topology of the polymer‐grafted surface revealed a distribution of surface clusters and surface elevations consistent with the expected broad molecular‐weight distribution for free‐radical polymerization. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 300–310, 2003     

纳米级氢氧化镍制备及电化学性能研究

介绍了一种通过合成草酸镍,进而生成β型纳米氢氧化镍的新的合成路线,从而达到大幅度提高镍氢电池正极放电容量的目的。使用X射线衍射（XRD）分析产品的晶型结构。从产品谱图中可以得知：由于特征衍射峰的出现可以判定该产品为β型,且由于（001）峰的宽化可以初步判定其为纳米级。通过透射电镜（TEM）可以看出产品粒径和形貌的具体特征,即产品为针状,长度为100～200 nm,直径为10～20 nm。将纳米级氢氧化镍制成电极,经过充放电测试可以发现电容量约为400 mA.h/g,远远高于球形微米级氢氧化镍的放电容量。     

Cesium salt of a heteropolyacid in nanotubular channels and on the external surface of SBA-15 crystals: preparation and performance as acidic catalysts

The Cs-salt of heteropolyacid with stoichiometry Cs_2.5H_0.5PW₁₂O₄₀ (CsHPW) was deposited selectively at the external surface of the SBA-15 silica microcrystals, inside its mesoporous channels and simultaneously at both location modes. The structure, texture and performance of these CsHPW/SBA-15 composites were compared with that of a reference bulk salt of the same composition. Location of CsHPW salt on the external surface of SBA-15 microcrystals leads to disintegration of its agglomerates increasing acidity of the catalytic phase. A novel preparation strategy consisting of grafting the basic Cs-species at the internal pores surface of SBA-15 stabilized the CsHPW phase inside the channels in form of 5–8 nm nanocrystals at 30–70 wt.% loadings. The catalytic tests demonstrated that insertion of the CsHPW catalytic phase inside the nanotubular channels of SBA-15 in combination with location of an additional amount of this phase at the external surface of SBA-15 microcrystals allows to increase the specific activity of this phase in MTBE synthesis, propionylation of anisole and alkylation of catechol with t-butanol by a factor of 1.5–3. This level of specific activity in combination with high total loading of catalytic phase >60 wt.% permit to get composite catalytic materials with catalytic activity higher by a factor of 1.2–1.5 with respect to the bulk CsHPW catalyst and stabilizing the catalytic phase against colloidization in polar media.     

Characterization and Sintering Behavior of Alkoxide-Derived Aluminosilicate Powders

Submicrometer SiO₂-Al₂O₃ powders with compositions of 46.5 to 76.6 wt% Al₂O₃ were prepared by hydrolysis of mixed alkoxides. Phase change, mullite composition, and particle size of powders with heating were analyzed by DTA, XRD, IR, BET, and TEM. As-produced amorphous powders partially transformed to mullite and Al-Si spinel at around 980°C. The compositions of mullite produced at 1400° and 1550°C were richer in Al₂O₃ than the compositions of stable mullite solid solutions predicted from the phase diagram of the SiO₂-Al₂O₃ system. Particle size decreased with increasing Al₂O₃ content. The sintered densities depended upon the amount of SiO₂-rich glassy phase formed during sintering and the green density expressed as a function of particle size.     

Effect of filler network on dynamic viscoelastic properties of uncured polymethylvinylsiloxanes filled with silica and carbon black

Dynamic properties of polymethylvinylsiloxane (PMVS) filled with filler‐blends composed of carbon black (CB) and silica (SiO₂) were investigated using an advanced rheometric expansion system. A variety of weight fraction of CB to SiO₂ were 0/100, 10/90, 30/70, 50/50, 70/30, 90/10, and 100/0, and a bifunctional organsilane, bis(3‐triethoxysilylpropyl)tetrasurfane, was used to facilitate the filler dispersion. The results reveal that the incorporation of CB/SiO₂ filler‐blends into PMVS result in a reduced Payne effect. This effect reaches a minimum when the ratio of CB/SiO₂ approaches 1, and then it began to rebound with the ratio increase. Meanwhile, a characteristic Newtonian viscosity plateau appearing in low frequencies also significantly decreases, depending on the amount of CB or SiO₂ added. On the basis of a simplified Fowke model, we ascribe this phenomenon to the deteriorated filler network, which is predominantly induced by the totally different surface activity between CB and SiO₂. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 99: 3477–3482, 2006     

Silica to Silicon: Key Carbothermic Reactions and Kinetics

The primary carbothermic reactions for the reduction of silica to produce silicon were defined and the reaction kinetics were determined. Most possible reactions between silicon oxide and carbon or carbon compounds were studied by a series of thermogravimetric analyses at temperatures up to 2000°C. Four key sequential reactions occur with SiC and SiO as intermediate reactants; two reactions involve SiO₂ and two involve SiO. Reaction rate versus temperature, activation energy, and preexponential factors were determined for each of six reactions involving SiO₂ or SiO. These kinetic studies show that SiO, when combined with either carbon or Sic, reacts in the gaseous state, and the sublimation of SiO is not the rate-limiting reaction for forming silicon.     

丙烯酸酯聚氨酯/SiO2纳米复合涂层结构与形态对其耐刮伤性影响研究

以四乙氧基硅烷(TEOS)作为主要前驱体,通过改变溶胶-凝胶工艺参数制得了结构和形态各异的丙烯酸酯聚氨酯/SiO2纳米复合涂层,利用TEM、SAXS等手段表征涂层的结构与形态,由洗刷前后涂层的失光率来表征耐刮伤性,详细探讨了纳米复合涂层耐刮伤性与SiO2相特征、有机无机相作用力及SiO2质量分数之间的关系。研究表明:丙烯酸酯聚氨酯涂层中引入纳米SiO2相后,耐刮伤性明显提高。有机相与SiO2相之间的作用力是影响涂层耐刮伤性的最重要因素,作用力越强,耐刮伤性越好。网络状纳米SiO2与颗粒状纳米SiO2相比,更有利于耐刮伤性的提高,且网络状纳米SiO2质量分数越大,耐刮伤性越佳,但SiO2相的致密度和尺寸对耐刮伤性影响较小。对于颗粒状胶体SiO2,在15~160 nm范围内,粒径对耐刮伤性没有明显影响;随着胶体SiO2粒子的质量分数增加,耐刮伤性先增大后减小。