Field studies on 32P movement and P leaching from flooded paddy soils in the region of Taihu Lake, China

Field experiments were done in two sites, Yixing and Changshu, Jiangsu province, China, to study P movement and leaching in flooded paddy soils. P movement in soil was investigated by using the KH2 32PO4 tracker method, and the amount of P leached from the soil layer in different depths was estimated by measuring P concentrations in the soil solution and saturated hydraulic conductivities in field. Determination was done about one month after P application. There was 46% and 42% of total 32P retained in the 0-5cm layer of soil in the Yixing site and in the Changshu site respectively. The 32P retained in the 25-30 cm layer was only about 1-2% of the total 32P added. Furthermore, 8.01% of 32P in the soil of Yixing site and 16.8% of 32P in the soil of Changshu site was lost from the layer 0-30 cm soil. The seasonal amounts of P leached from the top soil layer and from bottom layer are about 4.5-5.8% and 1.6-2.1% of the total P application, respectively. Changes of total P concentrations in soil solutions during rice growth showed that the fertilizer P applied before flooding of the paddy fields suffered a flash leaching loss and a slow leaching loss. We concluded that the fertilizer P could quickly move in the flooded paddy rice field and parts of it can enter into surface water and ground water. Unless the P application is well managed the risk of P loss and consequently environmental pollution exist.     

The gas-photocatalytic degradation of trichloroethylene without water

The photocatalytic degradation of gaseous trichloroethylene (TCE) without water has been studied. The degradation products were determined to be CO₂, HCl and Cl₂, and the reaction stoichiometry, was described as

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. The degradation rate was found to be linear with 0.16 power of the illumination intensity. When the TCE concentration was low (10¹⁴ mol L⁻¹ or a little more), its degradation rate model could be considered as first order kinetics. A mechanism of valence band hole oxidation was proposed.     

Effects of redox potential and pH value on the release of rare earth elements from soil

Equilibrium release experiments were conducted under three different pH values of 3.5, 5.5 and 7.5 as well as three redox potentials of 400, 0 and -100 Mv to investigate the influence of redox potential and pH value on the La, Ce, Gd and Y release of from the simulated-REEs-accumulation (SRA) soil. Oxygen and nitrogen were allowed to flow into soil suspension to adjust redox potential to a preset value, and 1 mol/l HCl or 1 mol/l NaOH solutions were added into the soil suspension to keep pH at a preset value. Results indicated that La, Ce, Gd and Y release increased gradually with the decrease of pH value or Eh, and the influence of redox potential on Ce was more remarkable than on La, Gd and Y. At the same time. It was observed that La, Ce, Gd and Y releases were positively correlated with the release of Fe and Mn, indicating that La, Ce, Gd and Y releases might originate from dissolution of Fe-Mn oxyhydroxides under reduction and low pH conditions. Moreover, it was found that alteration of pH value and redox potential might affect the change of La, Ce, Gd and Y species in the soil. The contents of La, Ce, Gd and Y in exchangeable fraction and Fe-Mn oxide fraction in the solid phase from soil suspension separation decreased with the decline of pH value and redox potential. Multiple stepwise regression analysis showed that exchangeable fraction and Fe-Mn oxide fraction predominately contributed to the La, Ce, Gd and Y release. Low pH value and redox potential were more favorable to La, Ce, Gd and Y releases following the change of their species. The La, Ce, Gd and Y contents in exchangeable fraction and Fe-Mn oxide fraction are the main contributors to their release.     

Distribution of mercury in the combustion products from coal-fired power plants in Guizhou,southwest China

Method 30B and the Ontario Hydro Method (OHM) were used to sample the mercury in the flue gas discharged from the seven power plants in Guizhou Province, southwest China. In order to investigate the mercury migration and transformation during coal combustion and pollution control process, the contents of mercury in coal samples, bottom ash, fly ash, and gypsum were measured. The mercury in the flue gas released into the atmosphere mainly existed in the form of Hg°. The precipitator shows a superior ability to remove Hg^p (particulate mercury) from flue gas. The removal efficiency of Hg²⁺ by wet flue gas desulfurization (WFGD) was significantly higher than that for the other two forms of mercury. The synergistic removal efficiency of mercury by the air pollution control devices (APCDs) installed in the studied power plants is 66.69–97.56%. The Hg mass balance for the tested seven coal-fired power plants varied from 72.87% to 109.67% during the sampling time. After flue gas flowing through APCDs, most of the mercury in coal was enriched in fly ash and gypsum, with only a small portion released into the atmosphere with the flue gas. The maximum discharge source of Hg for power plants was fly ash and gypsum instead of Hg emitted with flue gas through the chimney into the atmosphere. With the continuous upgrading of APCDs, more and more mercury will be enriched in fly ash and gypsum. Extra attention should be paid to the re-release of mercury from the reutilization of by-products from APCDs.

Implications: Method 30B and the Ontario Hydro Method (OHM) were used to test the mercury concentration in the flue gas discharged from seven power plants in Guizhou Province, China. The concentrations of mercury in coal samples, bottom ash, fly ash, and gypsum were also measured. By comparison of the mercury content of different products, we found that the maximum discharge source of Hg for power plants was fly ash and gypsum, instead of Hg emitted with flue gas through the chimney into the atmosphere. With the continuous upgrading of APCDs, more and more mercury will be enriched in fly ash and gypsum. Extra attention should be paid to the re-release of mercury from the reutilization of by-products from APCDs.     

利用有机质发酵产氢的影响因素与应用前景

煤、石油等化石能源的紧缺,使得氢气等可再生能源的开发与利用备受关注.生物制氢技术由于在获得清洁能源氢气的同时,还使得大量有机废弃物得到处理或净化,从而使得该技术成为当前研究的热点.总结了发酵产氢的微生物种类及产氢基质,阐述了不同有机物种类的发酵产氢机理,综述了温度、pH值、金属离子、气相条件及氧化还原电位等生态因子对发酵产氢的影响,并论述了生物制氢技术的发展方向和应用前景.     

鞍山市生态环境遥感评价指标体系

文中应用卫星遥感数据，通过选取合适的评价指标，建立适合本地区的生态环境质量监测与评价指标系统。为开发环境资源和建设生态环境提供管理和决策的依据。     

活性炭固定床电解槽研究

在分析电解槽能耗构成要素及形成原因的基础上 ,本研究开发出活性炭固定床电解槽用于污水处理。本研究以含酚废水为处理对象 ,主要进行了活性炭固定床电解槽与普通电解槽的能耗比较研究。结果表明 ,在相同酚去除率的情况下 ,活性炭固定床电解槽可节省能量 30 %～ 40 % ,具有显著的节能效果     

根据片段常数法估算有机化合物对虹鳟的LC50值

根据 2 58种有机物对虹鳟的 96h半数致死浓度 (LC50 )实测值建立了预测有机物对虹鳟LC50 的片段常数估算模型 .讨论了模型的误差和稳健性 .结果表明 ,有机物的片段常数及结构因子与虹鳟log1 /LC50 之间具有很好的定量关系 .可以根据化合物片段估算其对虹鳟的半数致死浓度 .最终模型的可决系数为 0 94 95,平均误差0 4 2个对数单位 .无论就单一化合物或化合物类别而言 ,模型均具有较高的稳健性     

桂林酸雨中不可溶成份的电镜分析

对广西省桂林市１９８８－０３－１６－１９８８－０３－２９出现的四次系统酸性降水，进行了降水的连续联样和过滤，用电子显微镜观测降水中的不可溶成分，共得到了１２种元素，即Ａｒ，Ｍｇ，Ａｌ，Ｓｉ，Ｐ，Ｓ，Ｃｌ，Ｋ，Ｃａ，Ｆｅ，Ｎｉ和Ｃｒ。用平均值法和聚类法，分析了桂林酸雨中１２种不可溶元素的重量谱特征，以及它们与降水系统之间的关系。     

Simulated seasonal movement of precipitation zone in rainy season over China and its change on CO_2-doubling

In this paper, an investigation of simulated monthly precipitations from April to September is made. Though the precipitations are sometimes overestimated or underestimated, the geographical advance and recession of precipitation zones are well simulated by the UKMO global climate model with a simple mixed-layer ocean. Main characteristics of large-scale precipitation distribution are changed less on CO2-doubling, but the change is significant in some regions. The change in precipitation threatens us while the dry region is imposed by rainfall defect or the wet region by abundant rainfall induced by CO2-doubling.