Partial Oxidation of Methane to Syngas over Calcined Ni–Mg/Al Layered Double Hydroxides

The catalytic partial oxidation of CH₄ to syngas was carried out over an Ni–Mg/Al mixed-oxide catalyst prepared from layered double hydroxide-type precursors. The catalysts were characterized by XRD, TPR, UV-DRS, XRF, BET and CHNS analysis. The effects of the catalyst composition and the calcination temperature on the catalytic performance and the extent of catalyst deactivation were investigated. Ni–Mg/Al oxide catalysts converted CH₄ into syngas efficiently with high selectivity. The catalyst performance was strongly related to the Ni particle size and the calcination temperature. The catalysts that were calcined at higher temperature exhibited a better catalytic performance. In conclusion, the NiAl₂O₄ spinel phase had a positive effect on the stability of the catalyst.     

关于生产精制元明粉的探讨

介绍了以山西运城南风自产芒硝为原料生产精制元明粉的几种工艺,以及国内外精制元明粉的市场及生产状况.精制工艺包括化学除杂法、原料优选法、重结晶法.结果表明,精制元明粉的生产过程实质是一个除杂、提纯过程：对于钙离子含量高的原料,可采用化学除杂法;对于氯离子含量高的原料,可采用氯离子富集法、冷冻法或洗涤法;镁离子较难去除,可采用水硝洗涤、冷冻法.     

不同形貌氢氧化镁的化学合成及影响因素

对不同形貌氢氧化镁的化学合成及外部生长环境进行了综述。尤其对影响氢氧化镁结晶性能和形貌起关键作用的因素，如碱性沉淀剂的选择、合成温度的确定、不同镁盐的影响、碱和镁盐的初始浓度及配比、水热处理、反应物的混合方式、晶形控制剂的加入等，进行了详细的阐述。     

反式肉桂腈的快速合成

以乙腈、氢氧化钾和苯甲醛为原料,在乙腈溶剂里,经搅拌回流(10 min)、碎冰水解、常压加热后减压蒸馏,快速合成反式肉桂腈,产率为48%~54%。研究了有机碳负离子亲核加成反应机理在有机合成中的运用。通过紫外可见光谱仪、傅立叶红外光谱仪和氢核磁共振仪对产物的结构进行了表征,证实产物正是目标产物。结果表明,依据有机碳负离子亲核加成反应机理,以氢氧化钾、苯甲醛和乙腈为原料,在温和的条件下即可快速合成反式肉桂腈。     

阻燃硅橡胶的研制

通过测定硅橡胶试片的离火熄灭时间及燃烧速率来判定热硫化硅橡胶的阻燃性。结果表明，氢氧化铝对热硫化硅橡胶具有良好的阻燃效果；随着氢氧化铝用量的增加，硅橡胶的物理机械性能下降。通过对氢氧化铝进行表面处理，并与氯铂酸等阻燃剂配合，可制得符合美国UL-94V-0阻燃标准的硅橡胶制品。在本实验条件下的最佳配比为：100份混炼硅橡胶，45份氢氧化铝，50份氯铂酸(以铂质量计／10^-6)，2份乙炔炭黑及铁锡复合氧化物，制品拉伸强度大于5MPa。     

Effect of cation exchange on the distribution and movement of cations in soils with variable charge. I. Effect of lime on potassium and magnesium exchange equilibria

The influence of Ca(OH)₂ on K and Mg exchange equilibria in three New Zealand soils was studied. Calcium hydroxide was mixed with each soil to raise the pH to about 6 or 7. For each Ca(OH)₂ treatment, K and Mg exchange isotherms were determined, from which the equilibrium activity ratios were derived. Exchange coefficients and solution activity ratios were calculated according to the Gapon convention.The addition of Ca(OH)₂ produced varying effects in the Gapon exchange coefficient for both K and Mg. The magnitude and direction of change in the exchange coefficient were related to the cation initially dominating the exchange sites, rate of Ca(OH)₂ addition, soil colloids contributing to the CEC and specific interactions of Ca with these soil colloids.Addition of Ca(OH)₂ reduced the equilibrium activity ratio of all soils. Changes in the bonding strength of K and Mg with increasing CEC were suggested as a possible mechanism for this decrease.     

氢氧化铝粉体表面化学改性的研究

综述了氢氧化铝粉体在应用领域存在的主要问题，解释了氢氧化铝粉体表面化学改性的机理。详细地介绍了国内外氢氧化铝粉体的表面化学改性的方法，主要包括酯化反应法、偶联剂法、表面活性剂吸附法以及聚合物包覆法。经研究表明，氢氧化铝粉体表面化学改性后扩宽了其应用领域，具有良好的前景。     

不同品种磷肥在土壤中的退化研究

对钙镁磷肥（FMP）、过磷酸钙（SSP）和部分酸化磷肥（PAPR）在河南郑州西岗沙土和河南西华县潮土中的退化情况进行了研究。     

剪切速率和静置时间对Fe-Al-Mg-MMH/钠质蒙脱土复合触变性体系触变性的影响

研究了测定条件对R=0.051的Fe-Al-Mg型混合金属氢氧化物(简称MMH)/钠质蒙脱土(简称MT)复合触变性悬浮体性质的影响.主要考察了高速剪切分散后,测定粘度(η)随时间(t)变化时采用的剪切速率(DL)和测定η前的静置时间(ts)的影响发现DL和ts的影响很复杂,ts=0,低DL时(10和170s-1)呈现复合触变性的体系,在高DL时(340、511和1022s-1)可呈现正触变性;DL增加,体系η逐渐降低.在所研究的ts范围内(0～2h),随ts的增加,体系分别由低DL时(10和170s-1)的复合触变性和高DL时(340、511和1022s-1)的正触变性皆转变为负触变性.低DL时(10和170s-1),η随ts逐渐降低;高DL时(340、511和1022s-1),η随t逐渐增高.对影响机理进行了初步探讨.     

Lanthanum-Magnesium and Lanthanum-Manganese Donor-Acceptor-Codoped Semiconducting Barium Titanate

BaTiO₃ powder doped with La donor and codoped with Mn or Mg acceptor was sintered at 1350°C/1 h in air. For Ladoped BaTiO₃, the room-temperature resistivity decreased to a minimum at [La³⁺] ∼ 0.15 mol%. For La-Mn-codoped BaTiO₃, the minimum resistivity occurred at [La³⁺] - 2[Mn²⁺] ∼ 0.15 mol%. When the ceramic was changed to a fine-grained insulator by high donor doping ([La³⁺] >0.15 mol%), its semiconductivity was restored, and the relatively homogeneous, coarse-grained microstructure recurred by codoping with either Mg or Mn acceptor, with the transition at [La³⁺] - 2[Mg²⁺] = 0.15 mol% or [La³⁺] - 2[Mn²⁺] = 0.15 mol%. The analogy of a compensation effect between La-Mn- and La-Mg-codoped BaTiO₃ suggested that Mn acceptor added to BaTiO₃ exists as Mn²⁺ ion in the bulk grain region; its influence on the positive temperature coefficient of resistivity behavior is then discussed.