应用D412螯合树脂治理含镍电镀废水的研究

本文研究了Ｄ４１２螯合树脂对Ｎｉ（Ⅱ）离子静态和动态的吸收性能,并且研究了使用Ｄ４１２树脂除去和回收电镀废水中镍的最佳条件。     

南亚热带丘陵土壤水分循环及其有效性的研究──Ⅳ.丘陵土壤贮水量的增减规律

根据三年定位实测资料,阐述0～100cm土层贮水量的动态变化,分析土壤贮水增减与降雨、蒸发的关系．观测结果表明,在气候正常年,雨季土壤贮水为增量,旱季土壤贮水为减量,但在坡地不同坡段和梯地不同梯级,土壤贮水增减有差异。在旱月土壤贮水减至最低,仅相当子田间持水量的55％～80％．因此在土壤水分管理上．应当密切注意土壤贮水减量最大的时期,以采取有效措施减少土壤水分蒸发,提高土壤水分利用率。     

亚铵法制浆黑液作肥料对水环境影响的研究

通过亚铵法制浆蒸煮黑液直接作农肥施于水稻田的研究,给出了不同施肥方式连续数天田间水和渗滤水中黑液污染物变化情况,定量描述了黑液作肥料直接施于水稻田对水环境的影响。     

广东省杨村华侨柑桔场土壤微量元素含量与分布的研究

采集并分析全场不同母质形成的有代表性的土壤样本142个.研究结果表明,各类土壤全B、Mo、Zn和Mn含量的平均值均低于全国平均值,全量Cu平均值高于全国平均值.有效B、Mo、Zn和Mn含量的平均值均低于临界值,有效Cu的平均值稍高于临界值;但66.7％的土样有效Cu含量低于临界值.硼、钼、锌和锰严重缺乏,铜多数缺乏.全场各类土壤的微量元素含量差异较大,各类土壤微量元素的垂直和水平分布特征不尽相同,尤其是垂直分布差异明显.从土壤微量元素的全量与母质的关系来看,以玄武岩、紫色砂页岩母质形成的土壤全量较高,砂砾岩母质形成的土壤全量中等,砂页岩和冲积物母质形成的土壤全量较低.     

Characterization of Organic Compounds in Compost-Amended Soil

Samples of compost-amended soil from waste dumping sites in Lagos Metropolis were extracted with dichloromethane (3 × 20 cm³) and the extract was evaporated at 35 °>C. The residue was extracted with 2,2,4-trimethylpentane, and portions of the solution were applied to a column containing silica gel from which aliphatic and aromatic hydrocarbons were eluted with n-hexane and toluene respectively. Analysis of the n-hexane fraction using gas chromatography showed the presence of a mixture of aliphatic hydrocarbons, ranging from C₉ to C₂₅, while ultraviolet analysis of the toluene fraction suggested 1,2-benzanthracene; 2,3-benzphenanthrene, chrysene and pyrene as polyaromatic compounds present in samples analyzed. The crude extracts were highly coloured and viscous. Total extractable organic residues in the 2,2,4-trimethylpentane extracts ranged from 36 to 89 mg g^-1 of soil.     

An Assessment of the Ecological Condition of Long Island Sound, 1990–1993

Data from the Environmental Protection Agency's (EPA) Environmental Monitoring and Assessment Program (EMAP) from 1990 to 1993 were used to assess the condition of the Long Island Sound (LIS) estuary. Ambient water, sediment and biota were collected during the summer months from 53 LIS stations using an unbiased sampling design. The design consists of two LIS subunits, LIS proper, and small estuaries (<2.6 km2) at the margins of the Sound. Selected indicators of condition included: benthic species composition, abundance and biomass; fish species composition and gross external pathology; sediment physical and chemical characterization and sediment toxicity; and water clarity and quality. Results of the four-year sampling indicated that 28(±11)% of the areal extent of LIS proper had a benthic index < zero (impacted) and 51(±12)% of the area of small estuaries was impacted. Analysis of the results of other indicators also shows that small estuaries were particularly affected. For example, 42(±10)% of the areal extent of small estuaries exhibited sediment toxicity, and significant chemical contamination was evident in 22% of the area of small estuaries. Low dissolved oxygen (D.O.) concentrations (<5 ppm), however, appeared to affect only the deeper open waters of western LIS. Approximately 48(±12)% of the areal extent of LIS proper documented exposure to at least moderate D.O. stress (<5 ppm). The overall results of this monitoring study indicate that significant anthropogenic impacts have occurred in LIS and that if remediation was to take place, specific localized sediment problems would need attention. Point source and non-point source nutrient inputs to the Sound, which are believed to be the primary causative factor for the observed hypoxic conditions, would also need attention.     

主动为环境监督管理服务

分析了一些县级监测站存在的只注重监测数据,缺乏主动为环境管理服务的思想,介绍了海门市则站主动为环境管理及时提供的监测数据,促进了环境监督管理。     

Heavy metal contamination in the vicinity of an industrial area near Bucharest

BACKGROUND, AIMS AND SCOPE: Chromium enters into the aquatic environment as a result of effluent discharge from steel works, electroplating, leather tanning industries and chemical industries. As the Cr(VI) is very harmful to living organisms, it should be quickly removed from the environment when it happens to be contaminated. Therefore, the aim of this laboratory research was to develop a rapid, simple and adaptable solvent extraction system to quantitatively remove Cr(VI) from polluted waters. METHODS: Aqueous salt-solutions containing Cr(VI) as CrO4(2-) at ppm level (4-6 ppm) were prepared. Equal volumes (5 ml) of aqueous and organic (2-PrOH) phases were mixed in a 10 ml centrifuge tube for 15 min, centrifuged and separated. Concentrations of Cr(VI), in both the aqueous and organic phases, were determined by atomic absorption spectrometry. The effects of salt and acid concentrations, and phase-contact time on the extraction of Cr(VI) were investigated. In addition, the extraction of Cr(VI) was assessed in the presence of tetramethylammonium chloride (TMAC) in 2-PrOH phase. Effects of some other metals, (Cd(II), Co(II), Cu(II), Ni(II) and Zn(II)), on the extraction of Cr(VI) were also investigated. RESULTS AND DISCUSSION: The Cr(VI) at ppm level was extracted quantitatively by salting-out the homogeneous system of water and 2-propanol(2-PrOH) using chloride salts, namely CaCl2 or NaCl, under acidic chloride media. The extracted chemical species of Cr(VI) was confirmed to be the CrO3Cl-. The ion-pair complex extracted into the organic phase was rationalized as the solvated ion-pair complex of [2-PrOH2+, CrO3Cl-]. The complex was no longer stable. It implied the reaction between extracted species. Studies revealed that salts and acid directly participated in the formation of the above complex. Use of extracting agents (TMAC) didn't show any significant effect on the extraction of Cr(VI) under high salting-out conditions. There is no significant interference effect on the extraction of Cr(VI) by the presence of other metals. The Cr(VI) in the organic phase was back-extracted using an aqueous ammonia solution (1.6 mol dm(-3)) containing 3 mol dm(-3) NaCl. The extraction mechanism of Cr(VI) is also discussed. CONCLUSIONS: Salting-out of homogeneous mixed solvent of 2-propanol can be employed to extract Cr(VI) quantitatively, as an ion-pair of [2-PrOH2+ * CrO3Cl-] solvated by 2-PrOH molecules. Then, the complex becomes 'solvent-like' and is readily separated into the organic phase. The increase of Cl- ion concentration in the aqueous phase favors the extraction. The 2-PrOH, salts and acid play important roles in the extraction process. There is no need to use an extracting agent at a high salting-out condition. RECOMMENDATIONS AND PERSPECTIVES: Chromium(VI) must be quickly removed before it enters into the natural cycle. As the 2-PrOH is water-miscible in any proportion, ion-pairing between 2-PrOH2+ and CrO3Cl- becomes very fast. As a result, Cr(VI) can easily be extracted. Therefore, the method is recommended as a simple, rapid and adaptable method to quickly separate Cr(VI) from aqueous samples.     

高压热水液化厨余垃圾的可行性研究

以高压热水为反应媒体处理厨余垃圾,得到液、气、固3种产物,并用GC-MS、GC-TCD和元素分析的方法对产物进行了表征。结果表明该技术处理厨余垃圾在实现减量化（达90.6%）和无害化的同时,可以达到资源化的目的。得出最优反应条件为：反应温度400℃,压力21.2 MPa,反应时间为40 min,优化的条件下固、液、气3种产物收率分别为21.5%、55.0%和5.2%。此外,对主要典型产物的形成机理进行了探讨。     

聚硅酸氯化铝处理皂素废水的研究

制备了聚硅酸氯化铝(PASC)絮凝剂,并用其进行了皂素废水处理实验。考察了絮凝剂投加量、pH值、搅拌速度对COD和浊度去除率的影响。结果表明,当絮凝剂投加量为9～13.5 mg/L、pH值5～7、搅拌速度150～250 r/min时,COD和浊度去除效果较好。最佳工艺条件为：絮凝剂投加量11.25 mg/L、pH值6、搅拌速度200 r/min。此时,COD去除率为93.7％,浊度去除率为97.5％。PASC的絮凝性能明显优于PAC。