柚园间种作物及施用不同有机肥对土壤与柚果的影响

柚树间种短期经济作物在提高柚园经济效益的同时,还可提高土壤的有机质和N、P、K养分质量分数,改善柚园小区气候,增加有机肥来源。间种物残余体作为绿肥,可显著地提高柚果产量和质量。     

土壤矿物固定态铵研究进展

主要从土壤中粘土矿物组成、有机物质、土壤水分、Fe的氧化还原、钾素状况及土壤粘粒的不同层面电荷、净表面电荷、表面电荷均匀性等方面就土壤中固定态铵的固定机制及其对作物的有效性的影响进行了综述;并对近年来土壤中固定态铵的测定方法作一评述。     

Effects of ecological factors on the diurnal activity rhythm of Yakutian black-capped marmots (Marmota camtschatica bungei) in the arctic

It is established that the activity of marmots (the genusMarmota) on the surface is timed to the daylight period. In the Arctic, under conditions of continuous illumination (the polar day), the diurnal rhythm of black-capped marmotsMarmota camtschatica bungei on the surface has a “daylight” pattern. The main external regulator of the diurnal rhythm is the altitude of the sun above the horizon. In the cold period, however, the effect of air temperature on animal activity becomes stronger.     

底泥中重金属毒性的室内孔隙水分析技术

根据孔隙水中重金属的浓度可以判定底泥中重金属的毒性但获得真正的底泥孔隙水十分困难。本文提供了一套简便易行的室内原状孔隙水取样技术,将碳化硅砂芯埋入底泥,添加表层水并静置９０ｄ,通过渗滤获得孔隙水,测定孔隙水中重的浓度,所得结果与微生态系统暴露试验中生物指示的重金属的毒性大小相吻合,与生物积累重金属的浓度显著正相关。     

聚苯乙烯基硫代磺酸钾树脂的合成及其与卤代烃的反应

由聚苯乙烯基磺酰氯树脂与硫化氢钾反应制备聚苯乙烯基硫代磺酸钾树脂（Ｉ）,树脂Ｉ与亲电的卤代烃反应,生成聚苯乙烯基硫代磺酸酯树脂（Ⅱ）,树脂Ⅱ经过乙硫醇处理,使卤代烃结构部分以不对称二硫醚的形式游离下来,用ＧＣ／ＭＳ对其结构进行鉴定。从不对称二硫醚的结构可推导出原卤代烃的结构,所制备的聚苯乙烯基硫代磺酸钾树脂的转化效率为１．１１ｍｍｏｌ·ｇ＾－１。     

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。     

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。     

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.     

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。     

50所长江沿岸高校实验废液排放情况调查与分析

目的：了解长江沿岸高校实验室废液排放情况及现状。方法：以问卷调查方式,对长江沿岸高校实验室操作程序、管理制度、废液排放情况进行调查。结果：38％的高校管理制度不完善,68％的高校实验操作不规范,44％的学校环保意识宣传不到位,62％的高校实验废液未处理就直接排放。结论：高校实验室正成为长江生态环境恶化的污染源．我国应制定和完善相关法律,加强实验废液处理,杜绝高校成为长江水质污染新的根源。