Guayule seedling response to nitrogen fertilizers

Slow growth and high seedling mortality limit direct seeding establishment of guayule (Parthenium argentatum G.). This study was conducted to assess seedling growth enhancement by the addition of different rates and forms of N fertilizers and Ca salts. Experiments were conducted in a greenhouse with cultivar 593 under both surface and subirrigated conditions using water low in salts (salinity of 0.8 dSm^–1, SAR of 5.0 and 10 mg Ca L^–1). Under surface-irrigated conditions, seedling height and fresh plant weight increased with N application to the irrigation water to 70 mg L^–1. The best seedling growth was observed when (NH₄)₂SO₄ was added in combination with CaCl₂ or CaSO₄. Progressively less growth was observed by addition of (NH₄)₂SO₄ alone, CO(NH₂)₂ plus CaSO₄, CO(NH₂)₂ alone and Ca(NO₃)₂. When seedlings were subirrigated, however, the best growth was observed with Ca(NO₃)₂. Intermediate growth was obtained with (NH₄)₂SO₄ plus CaSO₄ and lowest growth rates with (NH₄)₂SO₄ alone. These differential responses may be explained by the differences in leaching and volatile characteristics of the N forms. Growth enhancement from N and Ca additions increased with time with significant increases 45 days after seeding. Nitrogen application with Ca may be effective amendment in promoting subsequent growth of direct seeded guayule.     

废旧电池中有价金属回收利用探讨

随着中国经济的稳步发展和投资环境的不断优化,中国已成为电池的制造和消费大国,每年产生数亿只废旧电池。对废旧电池的回收利用已成为全社会关注的问题。介绍了废旧电池中有价金属的回收利用方法,着重介绍了锂离子二次电池正极材料有价金属的回收利用方法。指出,中国商品化的正极材料只有钴酸锂（LiCoO2）,这种正极材料钴含量高,且钴价值高,并且回收工艺可行,因此,从钴酸锂正极材料中回收钴等有价金属,对发展中国的循环经济具有重要意义。同时介绍了锂离子二次电池正极材料的研究现状。     

纳米碳酸钙在涂料中的应用研究

探究纳米碳酸钙先在溶剂中分散再与树脂进行调配的方法。利用正交设计法对其中高速搅拌法进行优惠条件实验，发现搅拌时间并非越长越好，优惠条件下涂料中纳米碳酸钙分散到原始粒径，涂料质量有较大提高。     

燃烧固硫反应的动力学和热力学及其影响固硫产物分解因素的研究

煤在高温条件下燃烧不利于固硫反应，并从热力学角度出发，得出了煤燃烧中钙基固硫剂反应自由能与温度的关系函数，由化学反应动力学得出院 硫酸钙分解反应的动力学方程及其相关参数，在还原性气氛中，从理论和实验上都证明了硫酸钙在较低温下会发生二次分解，理论分解温度与实际分解温度非常吻合，煤灰中氧化钙和三氧化二铝的存在，可以提高硫酸钙的分解温度同阳也给出了钙基固硫剂的应用条件。     

Cooperative effect of crystallization temperature and NaF addition in the formation process and hydrothermal stability of MCM-48 mesoporous molecular sieve

The hydrothermal stability of MCM-48 was conveniently and effectively improved by increasing the crystallization temperature and directly adding NaF to the synthesis gel. The crystallization temperature varied from 373 K to 403 K. The influences of NaF addition, crystallization temperature and crystallization time on the formation process and hydrothermal stability of MCM-48 were systematically studied here to solve the problem of poor reproducibility. Results from XRD patterns indicated that the crystallization temperature and crystallization time were very critical factors for the improvement of the hydrothermal stability besides NaF addition. The formation process of MCM-48 was significantly accelerated and the pore structure ordering was also greatly improved by increasing the crystallization temperature and F⁻/Si ratio. A high hydrothermally stable MCM-48 mesoporous molecular sieve was obtained after being crystallized at 393 K for 36 h in the presence of NaF, which endured the hydrothermal treatment in boiling water at least for 4 days. However, only an amorphous product was obtained when the crystallization temperature was further increased to 403 K. Results from Si MAS NMR, N₂ adsorption isotherms, TEM, Raman spectra and XRD patterns manifested that the improved stability of MCM-48 was attributed to the high silicates condensation degree and the excellent pore structure ordering. The possible reason for the successful formation of hydrothermally stable MCM-48 sample by controlling the crystallization temperature, time and F⁻/Si ratio was explained here.     

Investigation of transport phenomena in a hybrid ion exchange-electrodialysis system for the removal of copper ions

Hybrid ion exchange electrodialysis processes allow the removal of metal ions from dilute waste liquids and the recovery of more concentrated solutions. The work reported here was aimed at investigating the two steps in the treatment process, namely, adsorption of metal ions onto the packed bed of resin and electromigration (i.e., the transport of these ions in the complex system under the applied electrical field). The case of copper sulfate was investigated. Dowex resins with a cross-linking degree of 2 and 8% were used. The flux of copper through the resin bed and the current efficiency for ion transfer to the cathode compartment were determined as a function of potential gradient and copper ionic fraction in the bed. Apparent diffusion coefficients of Cu²⁺ in the overall system were deduced from the experimental data.     

Improvement of structural stability and electrochemical activity of a cathode material LiNi0.7Co0.3O2 by chlorine doping

In the process of Li⁺ intercalation-deintercalation, electron removal is accompanied simultaneously. Oxygen was found to compensate electron removal both in theoretical calculations and practical experiments. Chlorine addition to LiNi_0.7Co_0.3O₂ was expected to exchange electrons in that Cl⁻ was easier to lose electrons than O²⁻. LiNi_0.7Co_0.3O_2−xCl_x was identified as a pure hexagonal lattice of α-NaFeO₂ type by X-ray diffraction. X-ray photoelectron spectroscopy was used to analyze the influence of chlorine substitution on the oxidation state of transition-metal ions. Charge-discharge experiments and cyclic voltammetry confirmed that chlorine addition was an effective way to improve reversible capacity and structural stability in cycles.     

Ca-P仿生人工骨材料的设计与制备

本文设计了用磷酸钙生物陶瓷制备仿生人工骨的工艺路线 ,从原料合成、材料成型和烧结等讨论了仿骨材料的制备方法     

Structural and electrochemical characterization of mechanochemically synthesized calcium zincate as rechargeable anodic materials

Hydrated calcium zincate was synthesized by mechanical ball milling of ZnO and Ca(OH)₂ in water at room temperature. The structural and electrochemical properties of this material used as rechargeable anodic material were examined by microelectrode voltammetry, charge–discharge measurements and structural analysis. The results showed that during mechanical milling, ZnO, Ca(OH)₂ and H₂O reacted rapidly to form Ca[Zn(OH)₃]₂ · 2H₂O which was subsequently transformed to a stable structure CaZn₂(OH)₆ · 2H₂O. Since this composite oxide has lower solubility in KOH solution (<35 wt %) and better electrochemical reversibility than ZnO-based negative materials, the zinc anodes using this material can overcome the problems of shape changes and dendritc formation, and therefore exhibit improved cycling life.     

制备聚羟基氯化铝的一种新方法──以高岭土为原料，碳酸钙作盐基度调整剂制备条件的研究

本文研究了用碳酸钙作盐基度调整剂，从高岭土制聚羟基氯化铝的新方法．考查了酸浸液浓度及盐基度、反应温度和时间等因素对调整过程的影响。并制得了聚羟基氯化铝．