环氧乙烷及其精深加工产业现状与发展

综述了过去3年来国内外环氧乙烷生产及其精深加工产业现状和发展趋势,并初步探讨了我国今后环氧乙烷及其精深加工产业的发展趋势。     

0.91Pb(Zn1/3Nb2/3)O3-0.09PbTiO3的析晶行为及助溶剂法生长

研究了0.91Pb(znl/3Nb2/3)O3-0.09PbTiO3(PZNT91/9,摩尔分数)在不同组分和配比熔盐中的析晶行为及其对晶体生长的影响。发现B2O3,PbF2等助溶剂不利于钙钛矿相的析出;而BaTiO3-PbO复合体系虽然能够促进钙钛矿相析出,但晶体析出量很少;只有适当比例的。PbO助溶剂比较适合于生长具有铁电性的钙钛矿相PZNT91/9单晶。助溶剂法生长的工艺参数为:溶质与PbO助溶剂的摩尔比为l:l,泡料温度1 150-1 200℃,泡料时间10 h,晶体生长时降温速度0.8-2℃/h,当温度降到900℃时停止生长,以50℃/h快速冷却至室温。所得晶体为琥珀色,最大尺寸达φ30 mm×15 mm,其压电系数和机电偶合系数分别为2000 pc/N和0.92。     

X-ray photoelectron spectroscopic study of the oxidation and reduction of a cerium(III) oxide/cerium foil substrate

X-ray photoelectron spectroscopy has been used to examine the nature of the oxide overlayers on a passivated cerium metal foil as a function of a variety of oxidation and reduction treatments. Oxidation of a clean uncontaminated cerium(III) oxide surface is facile at room temperature and produces non-stoichiometric ceria (CeO_2–x) at oxygen doses as low as 10 L. At higher doses the overlayer thickens, and after a dose of 160 L the layer depth exceeds the Ce 3d photoelectron attenuation distance of about 20 Å. High pressure treatment of the foil in oxygen (0.5 bar at RT and 473 K) produces CeO₂ in a high degree of crystallographic order such that O 1s photoelectron intensities are increased above that expected from a randomly oriented powder. An attempt to reduce the CeO₂ layer formed by controlled oxidation with CO (633 K, 14 h, 0.6 bar) results in the formation of a carbonated surface layer. Results following attempts to reoxidise this layer are discussed.     

氧化钕填充尼龙6的结晶行为

利用示差扫描量热仪（ＤＳＣ）研究了氧化钕（Ｎｄ２Ｏ３）对尼龙６（ＰＡ６）等温结晶行为的影响。结果表明，Ｎｄ２Ｏ３在ＰＡ６体系中起到了异相成核作用，提高了ＰＡ６的晶体增长速率。     

Selective gas transport in miscible PPO-PS blends

The permeation rates of He, CO₂ and CH₄ though miscible blends of polystyrene and poly(phenylene oxide) at 35°C are reported as a function of pressure. Sorption isotherms for CO₂ and CH₄ are also presented. By using ratios of the permeabilities of the pure gases the separation factors for the gas pairs He---CH₄ and CO₂---CH₄ can be estimated. For both pairs the estimated separation factor goes through a prominent maximum, thus indicating that these blends are more permselective than expected from the behaviour of polystyrene and poly(phenylene oxide). This stems from mobility considerations rather than solubility effects and a qualitative free volume argument is proposed as an explanation. The sorption and transport data have been interpreted and correlated using the dual sorption-mobility models developed previously for glassy polymers. Since the commercial polystyrene used contained a small amount of mineral oil to improve flow behaviour, the effect of this additive on polystyrene properties was explored in some detail.     

Transformation of β-Ni(OH)2 to NiO nano-sheets via surface nanocrystalline zirconia coating: Shape and size retention

Shape and size of the synthesized NiO nano-sheets were retained during transformation of sheet-like β-Ni(OH)₂ to NiO at elevated temperatures via nano-sized zirconia coating on the surface of β-Ni(OH)₂. The average grain size was 6.42 nm after 600 °C treatment and slightly increased to 10 nm after 1000 °C treatment, showing effective sintering retardation between NiO nano-sheets. The excellent thermal stability revealed potential application at elevated temperatures, especially for high temperature catalysts and solid-state electrochemical devices.     

环氧丙烷-苯乙酮二元体系的恒温汽液平衡研究

采用改进的“p x法”汽液平衡测定装置测定二物质沸点差达 167.7℃的环氧丙烷 苯乙酮二元体系在3 0 0K、 3 0 5K下的p x数据 ;并用直接法计算确定平衡汽相组成y。     

滴加法制备铁黄颜料工艺研究

采用滴加法制备铁黄颜料，即采用硫铁矿烧渣直接制得的硫酸亚铁及硫酸亚铁结晶母液为原料。用空气作氧化剂，用氨水作沉淀剂制品种；在二步氧化中滴加氨水和硫酸亚铁结晶母液。探讨了亚铁浓度、空气流量等对晶种形成的影响，以及晶种比、空气流量、溶液pH、硫酸铵浓度等因素对铁黄生成的影响。确定了晶种制备和二步氧化的最佳工艺条件，即二步氧化中溶液pH控制在2．5～3．5，亚铁浓度控制在0．18～0．25mol／L的范围。检测结果表明：铁黄各项指标均达到原化工部HG／T2249--1991一级品标准。     

A Solder Alloy Filled Z-Axis Conductive Epoxy Adhesive

Epoxy adhesives filled with four different volume fractions of eutectic tin-bismuth solder alloy were prepared and the effect of filler content on the electrical and mechanical properties of these anisotropic electrically conductive adhesives was investigated. The results show that the adhesive containing the lowest amount of the filler alloy had the best combination of conductivity, insulation resistance and shear strength. The DSC-measurements suggested that the filler melts before the cure of the resin begins which allows the filler to wet and bond well to the conductors. This was verified by SEM/EPMA examinations. A temperature cycling test and high humidity, high temperature treatment were conducted on the best composite adhesive. The temperature variation had no effect on conductivity of the joints while humid and hot environment decreased the conductivity.     

Effect of cobalt oxide on surface structure of alumina supported molybdena catalysts studied by in situ Raman spectroscopy

A set of Co promoted 10% Mo/Al₂O₃ samples have been characterized by means of Raman spectroscopy under ambient as well as in situ dehydrated conditions. Under ambient conditions, the degree of the polymerization of surface molybdenum oxide species decreases with increasing Co loading. Under dehydrated conditions, the polymeric molybdenum oxide species is absent with the addition of only 0.2% Co. At low Co loadings (2%), before the formation of CoMoO₄ compound, the spectral features are very similar under ambient conditions. Dehydration causes the upward shift of the Mo=O symmetric stretching mode. A broad band around 920–930 cm^–1 was thus observed. This band has been suggested to be associated with the Co-Mo interaction species. In contrast to crystalline CoMoO₄, this species shows a reversibility on H₂ reduction-O₂ reoxidation treatments. From the results obtained, it is proposed that cobalt oxide interacts with the most polymerized molybdenum oxide species to form Co-Mo interaction species and/or crystalline CoMoO₄; therefore, the amount of the surface molybdenum oxide species decreases with a change in the molecular structure as a function of the Co concentration.