P_2O_5影响Na_2O-B_2O_3-SiO_2系玻璃结构与性质的特殊性

本文通过不混溶温度的确定,分相玻璃沥滤速率的测定以及NMR定量分析,研究了P_2O_6对Na_2O-B_2O_3-SiO_2系统玻璃结构和沥滤性质的影响。结果表明,P_2O_5在很大程度上促进钠硼硅分相玻璃的沥滤并非压抑“硼反常”所致,而是由以下三种因素综合作用的结果:(1)P_2O_5促进了钠硼硅玻璃的分相,使连通富硅相骨架尺寸增大;(2)P_2O_5的加入使富硅相骨架间隙中沉积的SiO_2量减少,减小了可溶相扩散阻力;(3)P_2O_5也使可溶相的溶解速率加快。     

Nitrate leaching from loamy soils as affected by crop rotation and nitrogen fertilizer application

Nitrate leaching as affected by cropping system/crop rotation, history of farmyard manure application or fertilizer nitrogen application (0 N, 0.5 N and 1 N) was studied at nine sites on loamy soils during 1986/87, 1987/88 and 1988/89. Soil solution from 80 to 90 cm soil depth was sampled every second week in the period November to May by the use of porous ceramic cups and analysed for NO₃-N and Cl. Climatical conditions were obtained from standard meteorological observations in the region. Drainage from soil profiles was calculated from measured and simulated values of precipitation and actual evapotranspiration, respectively.The results show that type of crop is of the utmost importance for the leaching magnitude of nitrate as 40% of the total variance in nitrate concentrations in the soil solution could be explained by the type of crop.The second factor of importance was the history of farmyard manure (FYM) application, which was able to explain 28% of the total variation in nitrate concentration in the soil solution. Nitrate concentration/leaching from arable land without FYM ever being applied was considerably lower than from arable land which received periodical FYM applications until the early 70's or from arable land which besides periodical FYM applications in the past presently still receives regular applications of FYM. Only about 1% of the total variation in nitrate concentration in the soil solution was explainable by the level of fertilizer nitrogen application.Differences between years explained 14% of the total variation in nitrate concentration in the soil solution due to differences between the years in soil temperatures and water run-off. The run-off during the autumn and winter of 1986/87, 1987/88 and 1988/89 was 95, 275 and 55 mm, respectively. As expected nitrate leaching increased with increasing run off. However, nitrate leaching at the 275 mm run off was considerably lower than expected, which seems explainable by a substantial denitrification. The soil at the sites in question seems thus partly to purify the soil solution for nitrate before it leaves the root zone at the observed high run off conditions.     

Effect of partial replacement of di(2‐ethyl hexyl)phthalate,by a polymeric plasticizer,on the permeability and leaching properties of poly(vinyl chloride)

Acrylonitrile butadiene rubber (NBR) was used as a polymeric plasticizer in poly(vinyl chloride) (PVC) for the partial replacement of di(2‐ethyl hexyl)phthalate (DEHP). The effect of this partial replacement on DEHP leaching from the PVC was evaluated at 10, 25, and 40°C. The study shows that the incorporation of NBR reduces the rate of DEHP leaching, the reduction being prominent at lower temperatures. Gas permeability of the NBR‐modified samples was also evaluated at the above temperatures using oxygen and carbon dioxide. A reduction in gas permeability is observed in NBR‐modified samples compared to the PVC plasticized with DEHP alone particularly in the case of carbon dioxide. Water vapor transmission rates of the NBR‐modified samples are higher than that of the control sample. The NBR‐modified PVC sample was found to be noncytotoxic in the in vitro cytotoxic evaluation both by direct contact and test on extract methods. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102:4720–4727, 2006     

Bauxite residue (red mud) increases phosphorus retention in sandy soil catchments in Western Australia

The Peel-Harvey estuary on the Swan Coastal Plain, Western Australia has become eutrophic partly because of the leaching of fertiliser phosphorus from sandy soils. The acid, coarse textured sandy soils are predominantly quartz, have a low iron and aluminium content and do not retain phosphorus. Red mud, derived from bauxite, is a by-product of the alumina industry and has the ability to retain phosphorus. Retention of phosphorus is enhanced when the red mud is neutralised with gypsum. Red mud has been suggested as a soil amendment to reduce phosphorus leaching.To investigate the reduction in the leaching of phosphorus from soils amended with red mud, weirs were constructed at the outlets from a pair of catchments to quantify the amount of phosphorus in the streamflow. Both catchments were deep grey Bassendean sand. One of the catchments was treated with 80 t/ha of red mud which had been neutralised with waste gypsum from the phosphate industry. The red mud was applied to the soil surface using conventional fertiliser spreading equipment. The other catchment was untreated.The red mud reduced phosphorus loss by 70% from 13.8 kg/ha on the untreated catchment, to 4.2 kg/ha on the treated catchment. Both catchments were treated with 20.4 kg/ha of phosphorus as superphosphate. The catchment treated with red mud also received a further 41.5 kg/ha of phosphorus from the phosphogypsum that was used to neutralise the red mud.Our results show that red mud reduces phosphorus leaching and is potentially a nutrient management option in sandy soils. Red mud has the potential to reduce the impact of agriculture on the estuarine environment and has implications for the continued expansion and intensification of agriculture in the Peel-Harvey catchment.     

富锰渣制备硫酸锰过程中除杂方法新探

研究了以富锰渣为原料,经硫酸浸出制备硫酸锰的工艺过程中除杂方法。分别探讨了以MnO2、H2O2、空气为氧化剂,以NH3.H2O、Ca(OH)2、富锰渣等为中和除杂剂,控制pH在5~6,中和除杂温度为50~60℃,保温时间1~1.5 h情况下,采用不同的除杂剂及除杂条件,取得了不同的除杂效果。     

软锰矿浸出制备软磁铁氧体用碳酸锰的研究

研究了以低品位软锰矿石为原料,配入植物粉料,用硫酸直接浸出软锰矿制备软磁铁氧体用碳酸锰的新工艺方法。探讨了软锰矿直接酸浸、含锰浸出液净化除杂、锰净化液碳化结晶等工艺条件。所制备的产品经X 射线衍射、粒度分析及化学成分分析等测试,结果表明,产品质量达到GB10503 89Ⅰ型品的要求。在优惠工艺条件下,锰的回收率达90%以上。     

金氰化浸出过程建模及实时优化自适应策略

以金氰化浸出过程为背景,基于物料守恒方程建立动态机理模型,用Tikhonov正则化方法估计动力学反应速度,进而辨识模型未知参数,有效降低了测量噪声对估计及辨识结果的影响;采用实时优化约束自适应方法减小模型参数失配对优化结果的影响.仿真结果表明,在模型参数失配时,所提出的方法仍能收敛到实际过程的最优设定点,不必求实际数据梯度,且受噪声影响小,便于实际应用,为湿法冶金全流程优化控制的顺利实施奠定了基础.     

An electrochemical study of the dissolution of gold in thiosulfate solutions. Part II. Effect of Copper

Thiosulfate has been considered as one of the most promising of the non-toxic alternatives to cyanide for the leaching of gold and much work has been carried out with the aim of understanding and improving the ammoniacal thiosulfate leaching process. In particular the behaviour of gold in thiosulfate solutions containing copper in the absence of ammonia has received little attention. It has been shown in this study involving electrochemical and leaching tests that copper ions catalyze not only the oxidation of thiosulfate but also the dissolution of gold in alkaline thiosulfate solutions. Electrochemical studies have shown that copper has a positive effect on the anodic dissolution of gold with increasing concentrations of copper resulting in higher dissolution rates of gold at a potential of 0.3V. Studies on the dissolution of gold powder in alkaline oxygenated thiosulfate solutions containing low concentrations of copper have shown that the role of copper in enhancing the dissolution rate of gold is possibly associated with the formation of a copper–thiosulfate–oxygen intermediate which is more reactive in terms of cathodic reduction than dissolved oxygen. The electrochemical experiments have been complemented by a leaching study which has shown that milling of gold powder in the presence of copper (added as ions, metal, or oxide) assists with the dissolution of gold in thiosulfate solutions.     

Exploration of mesoporous structure of tunisian raw and acid-leached phosphate ore particles

Rock phosphate fractions were examined for their porous structure by nitrogen adsorption. The pore size distribution and the shape of pores does not seem to depend on the particle size. The specific surface area values present two regions, one above and one below that of the particles with 125 μrn diameter. Particles of a given size were leached with dilute phosphoric acid (1.5 mass% P₂O₅) at 25°C. It was observed that there is a widening of the initial pores during leaching. The particles collected at the initial period of the reaction are pitted and those collected at the final period are disintegrated.     

Laboratory study of soil acidification and leaching of nutrients from a soil amended with various surface-incorporated acidifying agents

Granular S, finely-ground S, iron sulphate and aluminium sulphate were added at two rates to the surface (0–6 cm) of a soil and acidification and leaching of nutrients were measured over 12 months in a laboratory study. Iron and aluminium sulphate both rapidly lowered soil pH in the top 0–6 cm of the soil. There was little difference in soil pH after 3 and 12 months reaction of these two amendments. In contrast, for granular S and finely-ground S there were clear decreases in soil pH between 3 and 12 months reaction with the soil. Finely-ground S was oxidized in the soil faster than granular S and therefore had a more acidifying effect. The top 0–6 cm of the soil was acidified by all the agents used but the deeper soil was less affected. The only treatments which lowered the pH of the 12–18 cm layer below pH 6 were the high rates of iron and aluminium sulphate. Soil acidification resulted in a decrease in exchangeable Ca, Mg and K, an increase in exchangeable Al and a decrease in effective CEC in the acidified soil layers.At both levels of addition, total ionic strength of percolates from the soil followed the order: aluminium sulphate = iron sulphate > finely gound S > granular S > control and was higher at the higher rate of addition. The pH values of percolates followed the order: control > granular S > finely ground S > iron sulphate = aluminium sulphate and were lower at the higher rate of addition. For the amended soils there was a very close relationship between the pattern and total amounts of SO ₄ ^2- and Ca²⁺ leached.It was concluded that granular S is not an effective acidifying agent since it is oxidized very slowly in the soil and that acidfying agents should be incorporated to the depth that acidification is required.