偏高岭石碱溶合成方钠石相变过程及吸附特性

方钠石具有笼型结构和比表面积大的特性,使其吸附能力较强。以偏高岭石和NaOH为原料,通过碱溶法合成了羟基方钠石,探讨了NaOH浓度、反应温度、反应时间和液固比对合成方钠石的影响。采用XRD、SEM、IR和NMR对碱溶过程的产物进行了表征；探讨了方钠石对Al³⁺的吸附特性。结果表明,反应温度对方钠石合成影响最大,NaOH浓度次之,液固比影响较小,升高反应温度和增大NaOH浓度可缩短反应时间。碱溶过程中,偏高岭石中的活性铝、硅优先溶解于NaOH溶液,随着反应的推进,溶液中的铝、硅达到一定浓度后会发生缩聚反应形成前驱体胶凝相。NaOH浓度对前驱体胶凝相的转变影响显著,低浓度时,胶凝相主要转变成沸石相；高浓度时则转变为方钠石相,反应的本质是处于亚稳定状态的沸石相与NaOH反应形成方钠石相。吸附特性试验表明,方钠石对Al³⁺的吸附符合Langmuir模型,其吸附率高达99.9%,最大吸附量达89.77 mg/g。     

Assessment of tracing element characteristics of F-type fly and bottom ash mixture

Presently, fly ash–water slurry is transported to ash disposal site at very low solid concentration of approximately 15–20% (by weight), resulting in huge water and energy wastage which leads to several environmental and health problem. The production of a large amount of the toxic metal elements in the ash disposal system of the thermal power plants can pose negative environmental effects on human health and on plants. In the present study, an attempt has been made to investigate the leaching characteristics of fly ash at higher concentrations. The bottom ash was taken as an additive in the proportion of 10, 20, and 30% (by weight) to enhance the leaching characteristics of fly ash. The solid concentration of fly ash suspension was taken in the range of 40 to 60% (by weight). The addition of additive helps to reduce the tracing metal concentration of fly ash. Leaching experiment data show that leachate concentration of all tracing elements present in fly ash reduced maximum with 20% addition of bottom ash (by weight). The present study helps to improve the ash disposal system of the thermal power plant and to minimize the environmental impact.     

铂钯精矿中氯化银的浸出预处理研究

铜阳极泥分铜液所得铂钯精矿中的银主要以氯化银(AgCl)形态存在，可用氨水或亚硫酸钠作为浸出剂去除银。绘制了Ag⁺与NH3、SO2- 3配体组分图，结合电位-pH图分析表明，氨浸的pH值范围为7.7~13.5，亚硫酸钠浸出宜在中性或碱性条件下进行。优化条件实验结果表明，银的氨浸浸出率为95.3%，碲浸出率为14.9%，有微量铂、钯浸出；以亚硫酸钠为浸出剂，银的浸出率为97.3%，碲浸出率为11.5%，金、铂和钯均不被浸出。亚硫酸钠更适于作为铂钯精矿预处理除银的浸出剂。     

Concept for a Hydrometallurgical Processing of a Copper-Cobalt-Nickel Alloy Made from Manganese Nodules

The processing of manganese nodules for the production of raw materials has been a subject of research for many decades. The nodules contain many valuable metals like copper, cobalt and nickel. In recent years, the German Federal Institute for Geoscience and Natural Resources developed a process for the processing of manganese nodules based on a combined pyro- and a hydrometallurgical route. Clausthal University of Technology was assigned to develop the hydrometallurgical process for the treatment of a FeNiCuCo alloy. The developed process consists of pressurized sulfuric acid leaching with the suppression of hydrogen gas formation, precipitation and solvent extraction.     

PVC⁃U排水管道中重金属铅的浸出研究

研究了3种添加铅稳定剂的铅总量和硬聚氯乙烯（PVC?U）管道产品在不同时间，温度及pH下的浸出规律，并讨论了浸出机理。结果表明，3种产品浸出规律一致：铅浸出量随时间增加先增加后减少，浸出4 h时浸出量最大；温度对铅浸出量影响显著，铅浸出量随温度的增加持续增加；铅在强酸性环境的浸出量大于在强碱性环境下的浸出量，在偏碱性环境下的浸出量最少。     

Purified high‐sulfur coal as a fuel for direct carbon solid oxide fuel cells

The use of low‐rank coal in a clean and efficient manner is a major challenge facing the current coal technology. A high‐sulfur coal with 4.5 wt% sulfur is chosen to examine the compatibility of the pristine coal and the purified contrast with a solid oxide fuel cell (SOFC) with nickel cermet anodes. Desulfurization of the pristine coal is performed by molten caustic leaching method with a removal ratio of 80%. Analyses of the physicochemical properties of coal samples indicate that the purified coal has a more favorable structure and higher Boudouard reactivity, which is suitable as a fuel for fuel cells. The assessment of electrochemical performance reveals that the purification treatment not only makes the peak power density of SOFCs improve from 115 to 221 mW cm^?2 at 900°C but also extends their durability from 1.7 to 11.2 hours under a current density of 50 mA cm^?2 at 850°C with a fuel availability increasing from 6.25% to 40%. The postmortem analyses show that far less deposited carbon and nickel sulfide are observed on the anode surface. The fuel‐based investigation reveals that the purified coal is a promising fuel for direct carbon fuel cells.     

多级深度还原法制备Ti6Al4V合金粉体的基础研究

目前Ti6Al4V合金粉体的生产方法主要有雾化法、机械合金法和氢化脱氢法,它们都以Kroll法生产海绵钛为基础。使用钛的氧化物作为原料的熔盐电解法和金属热还原法仍处于研究阶段。本文依据变价金属Ti和V的氧化物在还原过程中逐级还原的特性,提出使用金属氧化物(TiO₂, V₂O₅)作为原料的多级深度还原法制备Ti6Al4V合金粉体的新思路。首先计算了TiO₂-V₂O₅-Mg-Ca体系的吉布斯自由能变,结果表明先进行镁热自蔓延反应,后进行钙热深度还原反应制备Ti6Al4V合金粉体在热力学上具备可行性。然后通过实验进行了的验证。镁热自蔓延反应产物酸浸后除去MgO可得到氧含量为15.84%的多孔Ti-Al-V-O前驱体。配入金属Ca后进行深度脱氧可得到低氧Ti6Al4V合金粉体(Al: 6.2wt.%, V: 3.64wt.%, O: 0.24wt.%, Mg: 0.01wt.%, Ca: < 0.01wt.%)。     

粗碲粉加压氧化浸出工艺研究

针对上游工序发生改变，研究了采用加压氧化浸出工艺处理粗碲粉。采用单因素试验考察了液固比、游离碱度、反应压力、反应温度、反应时间对浸出效果的影响，确定最佳工艺条件为：液固比10，游离碱浓度40g/L，反应压力0.8MPa，反应温度75℃，氧化时间2h。试验结果表明碲的浸出率可达95.45％，金银富集在20倍以上。     

Accelerating the decarbonization of carbonaceous gold ore by suspension oxidation roasting towards the improvement of gold leaching efficiency

Eliminating the gold preg-robbing effect of carbonaceous matter in carbonaceous gold ores is crucial for gold leaching. In this study, suspension oxidation roasting was proposed to accelerate the decarbonization of carbonaceous gold ore. The characteristics of oxidation reaction process and gas release were analyzed by TG-DTA-FTIR. The phase transformation and microstructure evolution of samples during roasting were analyzed by XRD, SEM and BET. The results show that the gold preg-robbing effect was eliminated after the gasification of carbonaceous matter, and the CaO generated by decomposition of carbonates can effectively capture the SO₂. After roasting for 75 min at 650 °C in a 20% O₂ atmosphere, the total carbon removal rate reached 99.42%, the distribution of exposed gold increased from 28.85% to 77.10% and the gold leaching efficiency increased from 4.55% to 84.83%. In addition, about 70% sulfur was mainly fixed in the roasted products in the form of sulfate. Therefore, the suspension oxidation roasting process is an efficient and clean pretreatment method for carbonaceous gold ores.     

Enhanced efficiency fertilisers: a review of formulation and nutrient release patterns

Fertilisers are one of the most important elements of modern agriculture. The application of fertilisers in agricultural practices has markedly increased the production of food, feed, fuel, fibre and other plant products. However, a significant portion of nutrients applied in the field is not taken up by plants and is lost through leaching, volatilisation, nitrification, or other means. Such a loss increases the cost of fertiliser and severely pollutes the environment. To alleviate these problems, enhanced efficiency fertilisers (EEFs) are produced and used in the form of controlled release fertilisers and nitrification/urease inhibitors. The application of biopolymers for coating in EEFs, tailoring the release pattern of nutrients to closely match the growth requirement of plants and development of realistic models to predict the release pattern of common nutrients have been the foci of fertiliser research. In this context, this paper intends to review relevant aspects of new developments in fertiliser production and use, agronomic, economic and environmental drives for enhanced efficiency fertilisers and their formulation process and the nutrient release behaviour. Application of biopolymers and complex coacervation technique for nutrient encapsulation is also explored as a promising technology to produce EEFs. © 2014 Society of Chemical Industry