锌精矿制酸三级旋风除尘器的设计与实践

介绍了锌精矿制酸系统采用三级旋风除尘器替代电除尘器的设计及运行情况。为了提高旋风除尘器的除尘效率，硫酸系统各工序作了适当调整。运行实践表明，三级旋风除尘器除尘效果良好，硫酸系统能长期稳定运行。     

均匀设计试验方法及其在Ni-P-MoS2化学镀上的应用

均匀设计是基于试验点在整个试验范围内均匀散布的一种试验设计方法。介绍了该法的特点及其软件的基本功能与基本操作过程。从均匀设计试验方案的建立、试验结果的回归分析及优化、镀液最佳配方的试验验证3个方面介绍了均匀设计法在Ni-P-MoS2化学复合镀中的应用，并得到了最佳的Ni-P-MoS2化学复合镀液配方。该法应用于化学镀的工艺试验，简便可行。     

碳铵法制备纳米氧化锌的研究

一种纳米氧化锌的制备方法，其过程包括：以硫酸锌和碳酸铵(或碳酸氢铵和氨水)为原料中和制备碱式碳酸锌，碱式碳酸锌经水洗除掉硫酸根后，再醇洗、干燥、煅烧，制备了纳米氧化锌。经表观密度、比表面积、孔容积和透射电镜(TEM)的测定，确定了研制的物料为纳米氧化锌，粒子峰值为10～20nm。     

我国锌盐工业的现状与展望

阐述了我国锌盐工业的发展现状、存在的问题和面临的机遇与挑战,提出了发展锌盐工业的建议。     

硫代磷酸/伯胺N1923协同萃取锌和镉的机理

有机硫代磷酸/伯胺N1923协同萃取锌、镉的萃取率随pH的变化较为反常，可能因伯胺N1923与硫酸作用进而聚为反向胶束. 实验表明，如以(N1923)n.H2SO4表示反向胶束的实验式，N1923与H2SO4比值n多为3左右，可能与空间效应相关. 萃取机理为: M2+(a) +2BHA(o) + (2/n)SO42–(a) = MA2(o) + (2/n)(Bn.H2SO4)(o) + 2(1–2/n)H+(a)， n=3, 4, 5.     

氧化锌对阿利特和硫铝酸钙的形成及共存温度范围的影响

借助差热分析、X射线衍射及化学分析等,研究了ZrO对含硫铝酸钙的硅酸盐水泥熟料中阿利特和硫铝酸钙矿物形成及共存温度范围的影响.结果表明:在生料中掺入1%(质量分数)ZnO,可降低阿利特的形成温度,并促进低温下硫铝酸钙矿物的形成;1 300℃时阿利特生成的质量分数达59.23%,较未掺ZnO样品提高14.76%;掺入ZnO后,扩大了硫铝酸钙与阿利特矿物的共存温度范围,达50℃.     

Contributions to the Ohmic Drop in the Electrolysis of ZnCl2 in a Molten Chloride Electrolyte

The electrowinning of zinc from zinc chloride with a molten chloride electrolyte was investigated. The electrolysis of zinc chloride shows ohmic limitations. The energy consumption is to a large extent determined by the anodic reaction, the evolution of chlorine. The chlorine gas plume was visualised in a see-through furnace and images were analysed to determine the plume angle. This parameter serves as an input parameter for a model to determine the ohmic contributions of the electrolyte, the plume and a layer of chlorine bubbles sticking to the anode, as well as the plume velocity. The results indicate that the major contribution (60%) to the ohmic drop is due to a stagnant layer of bubbles growing and sticking to the anode, thereby decreasing the effective anode area by coverage. The plume velocity influences coverage characteristics to some extent, which influences the ohmic drop.     

Coal liquefaction by in-situ hydrogen generation.: 2. Zinc-water model compound reactions

Model compound studies were carried out to elucidate the reaction mechanisms taking place during the liquefaction of coal with the hydrogen produced from the reaction of zinc and water. In compounds of the type Ph-(CH₂)_n-Ph the splitting of the aliphatic bridge was easier with higher n values. Ether type compounds such as diphenylether were unreactive although the C-O bond in dibenzylether was easily cleaved. Condensed ring aromatic compounds gave low conversion with hydrogenation being facilitated by an increase in ring number. Phenolic compounds such as phenol did not react well, but the reactivity increased with increase in aromatic ring size. The cleavage of the aliphatic bridge was accelerated by the OH group, for example, in the case of 4-hydroxydiphenylmethane bond scission was about 15 times higher than that of diphenylmethane. Heterocyclic compounds were unreactive.     

Structure of Atomic and Molecular Adsorbates on Low-Miller-Index ZnO Surfaces Using X-ray Absorption Spectroscopy

We review our X-ray absorption spectroscopy studies of adsorbate geometries on the O-terminated (000 ) and Zn-terminated (0001) basel faces, as well as the non-polar (10 0) prism face of ZnO. Studies employing near-edge X-ray absorption fine-structure (NEXAFS) and surface X-ray absorption fine-structure (SEXAFS) are included.     

Quantitative Analysis of Zinc Vaporization from Manganese Zinc Ferrites

Zinc vaporization of Mn-Zn ferrites was quantitatively characterized in terms of oxygen partial pressure P _O2, temperature, grain size and sample geometry. The amount of zinc loss was measured as a function of time at various temperatures by a thermogravimetric method. The weight loss due to irreversible zinc vaporization showed a linear behavior with time and increased exponentially with temperature. The observed weight loss due to zinc evaporation at 1100°C was small, whereas a significant weight change was detected at 1200°C. The weight loss was even greater in a reducing atmosphere ( P _O2= 5 × 10⁻⁵). Below 1300°C, the diffusion of elemental zinc was sufficiently fast to compensate the zinc loss at the interface region, resulting in a linear dependence on time. At temperatures ≥1400°C, the weight change no longer followed the linear dependence and showed a rather parabolic behavior with a concave upward slope. The core shape and the gas flow around ferrite cores were important factors that affected the rate of zinc vaporization, but not the grain size.