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.     

干旱区2种猪毛菜萌发过程对水盐胁迫的生态响应

在实验室内模拟研究的基础上,运用生理生态学的原理,研究了水盐胁迫对钠猪毛菜(salsola nitraria)和散枝猪毛菜(salsola brachiata)种子萌发的影响,结果显示,钠猪毛菜与散枝猪毛菜种子萌发的最适温度分别为25 ℃和15 ℃.在盐溶液和PEG溶液中,2种种子的萌发规律相似,即随着水势的降低,萌发率和萌发速率下降.在盐胁迫下钠猪毛菜和散枝猪毛菜种子萌发的最低水势接近-7.2 MPa;在水分胁迫下2种种子萌发的最低水势均未超过-2.0 MPa,其中,钠猪毛菜种子表现出较强的耐水分胁迫能力.在相同水势条件下,PEG对2种猪毛菜种子萌发的抑制程度显著大于等渗NaCl,说明渗透胁迫是影响2种植物种子萌发的主要因素.     

Dynamic taxation schemes to manage irrigation-induced salinity

This paper uses a dynamic model to explore the issue of irrigation-induced salinity, which puts irrigation at risk in most irrigated areas throughout the world. We address the design of instruments that an irrigation district board could implement to induce irrigators to take sustainable irrigation decisions. In our approach, the irrigators located above an aquifer participate in the accumulation of groundwater, a stock pollution. We analyse input-based instruments to induce the agents to follow the optimal stock path.     

复合污染中Triton X-100在膨润土/水界面上的吸附行为

研究了水溶液中膨润土对非离子表面活性剂Triton X-100(X-100)的吸附,重点探讨了阳离子表面活性剂CPC、阴离子表面活性剂SDBS、中性无机盐NaCl及温度对膨润土吸附TX-100的影响.结果表明,Na基膨润土吸附TX-100的效果好于Ca基膨润土;低浓度CPC对膨润土吸附TX-100具有增强作用,当CPC初始浓度大于l0000 mg·L-1(平衡浓度Ce约为1CMC)时具有抑制作用,当CPC浓度低于3000 mg·L-1(Ce约为0.03CMC)时,TX-100吸附量与CPC浓度成线性正相关.SDBS能显著降低膨润土对TX-100的吸附,原因是溶液中SDBS与TX-100混合胶束的形成能阻止TX-100与膨润土硅氧表面间的氢键作用及在其表面形成胶束.NaCl的存在可以大大提高膨润土对TX-100的吸附,去除率由56%提高到99%以上.膨润土对TX-100的吸附随温度升高吸附量增大,其吸附热为12.68 kJ·mol-1,标准自由能的减小和熵值的增大是TX-100在膨润土上吸附的推动力.实验结果对用膨润土处理含表面活性剂废水具有一定的理论价值.     

应用原子力显微镜研究盐度对棕囊藻生长的影响

研究不同盐度梯度下棕囊藻的生长,实验设计了10个盐度梯度,结果表明:在盐度8~32范围内,棕囊藻的生长正常,最佳生长盐度为16,当盐度低于8或高于32时,藻的生长明显受到抑制,细胞数量增长缓慢,最大细胞数远低于16盐度组。研究发现:棕囊藻在盐度为0的环境下仍能缓慢生长,说明海洋中的棕囊藻赤潮在内陆的淡水湖也可能暴发,用原子力显微镜研究比较盐度为0及36的棕囊藻细胞表面形态,发现两者差异较显著,前者藻细胞的直径大于后者,且后者藻细胞表面形成了明显的塌陷。     

洪水入海对养殖环境影响的数值分析

基于三维流体动力学和热力学原始方程 ,采用σ坐标变换技术 ,建立了三维斜压场数值模型。模型采用ADI格式求解连续方程和动量方程 ,采用FS法和TVD格式求解各标量方程 ,从而使模型的精度提高到二阶 ,并且节省运算时间。利用建立的三维斜压场数值模型 ,对鸭绿江洪水期形成的低盐水体的分布进行了数值模拟 ,进而分析了鸭绿江洪水入海对黄海北部海域的海水养殖业的可能影响。鸭绿江特大泄洪形成的超低盐混浊水体入侵 ,是筏养扇贝致死的主要原因。及时预报大洪水影响下的低盐水体分布 ,可有效地防止洪水污损灾害。     

2024铝合金连接结构两种防护涂层耐蚀性研究

目的研究铝合金两种防护涂层在5%NaCl盐雾环境下的腐蚀疲劳性能。方法针对在两种涂层防护作用下的2024铝合金连接结构,开展实验室加速试验,采用"腐蚀环境-疲劳加载"交替循环的试验模式,得到铝合金两种防护涂层在5%NaCl盐雾环境下的腐蚀疲劳寿命值,对比分析涂层体系对铝合金连接结构的腐蚀疲劳寿命影响。结果 5%NaCl盐雾环境对于铝合金连接结构疲劳寿命有较大影响,相较于传统涂层,纳米涂层在5%NaCl盐雾环境下的防护效果更好。结论纳米涂层表面破坏后快速生成的致密氧化膜能有效提高涂层的耐蚀性能。     

城市污水处理厂污泥沉降影响因素研究

研究总结了目前城市污水处理厂污泥沉降影响的因素，概括总结了pH值、溶解氧、温度、盐度等环境因素以及磁场等外部环境因素对不同性状污泥的沉降影响。为污泥沉降脱水最佳条件提供了研究思路，也为污泥后续机械脱水提供了基础。     

煤矸石制取聚羟基氯化铝的研究

介绍了用煤矸石制取聚羟基氯化铝的方法,研究了酸浸、调整盐基度等过程的最佳工艺过程。