土柱淋洗法修复铬污染土壤的水力梯度优化试验

针对重金属污染土壤的修复,淋洗法是一种比较成熟的方式,但目前研究主要聚焦于淋洗剂的选择,而关于水力停留时间对淋洗效果影响的研究相对较少.水力梯度是影响水力停留时间的重要因素,优化水力梯度能够缩短修复周期,降低淋洗成本,有效提高淋洗效率,为现场淋洗修复工程应用提供参考.本文针对人工制备的不同质地的铬污染土壤进行了土柱淋洗...     

利用烧结炼铁工艺环保处理铬渣

论述了铬渣的产生、组成、特性,利用冶金生产中的烧结炼铁生产工艺对其进行解毒的机理、配加处理铬渣的工艺流程、配加比例和对烧结矿生产工艺参数的影响情况,利用该法对其解毒处理的优势,及解毒处理中防止二次污染和个人防护措施.     

铬盐废水蒸发系统腐蚀突变与缓蚀工况研究

针对铬盐废水蒸发系统运行过程中的腐蚀问题,采用失重法、pH值检测、扫描电镜(SEM、EDS)和XRD等手段,模拟研究了温度、Cr3+质量浓度对20#碳钢腐蚀速率、腐蚀产物的影响,并从废水pH值和形貌分析角度探索腐蚀速率发生突变的原因.研究表明:废水Cr3+质量浓度在150～180 mg/L范围,碳钢腐蚀速率发生突增,废...     

Heavy metals' content of automotive shredder residues (ASR): evaluation of environmental risk

Every year between 8 and 9 millions of vehicles in the European Union arrive to their end of life. Car wastes can have a very high metal content, falling into hazardous waste class. A preliminary evaluation of these wastes could be made by metals' leaching test runs which is the main objective of the present study. Evaluation of the total metal content was carried out by X-ray fluorescence and the mobility of these metals using two simple standardized extractions such as the TCLP (Toxicity Characterisation Leaching Procedure) of the US EPA and the German leaching test DIN 38414-S4. Additionally, an extraction test with acetone was performed in order to recognise metals bounded to organic matter. The results show that the total metal content of the ASR can overpass the established values for inert residues. Lead and zinc contents are fairly well correlated with grain-size, whilst other metals' contents do not exhibit clear grain-size dependence.     

典型铬渣简易掩埋场铬渣及土壤铬污染特征和处置分析

通过钻孔采样分析,研究了典型铬渣简易掩埋场地下铬渣及土壤铬中Cr6 、总Cr的分布特征和污染状况,结果表明,铬渣简易掩埋场铬污染程度严重,引起了周边和地下深部较大面积的土壤污染,深度达到了地下的基岩.铬含量在土壤层剖面中分布呈现规律性变化,即随土壤深度增加,Cr6 、总Cr含量逐渐下降,但绝大多数超过了危险废物毒性鉴别标准.从铬污染程度上看,总体上存在铬渣>土壤>人工填土.在此基础上,提出了铬渣及污染土壤的处置方式,为铬渣污染治理和资源化利用提供科学依据.     

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.     

松花江野生鱼类重金属残留分析与评价

以松花江流域的野生鱼类为研究对象,在松花江流域选取松林、大顶子山、佳木斯3个具有代表性的点位,在2014—2016年的每年5月底6月初采集鲤鱼和鲫鱼样品,3年内共制备45个鲤鱼单样,44个鲤鱼混样,30个鲫鱼混样,共计119个。采用电感耦合等离子体-质谱法对鱼类肌肉组织中残留的As、Cd、Cr、Pb、Hg 5种重金属进行检测。检测结果显示,As、Cd、Cr、Pb、Hg 5种重金属全部检出,检测结果全部达标,达标率为100%。根据检测结果采用单因子指数法和金属污染指数法等评价了松花江流域鱼体重金属残留状况及食用安全性,评价结果为松花江流域鱼类重金属残留量相对较少,鱼体健康,食用安全。     

Vermicomposting as an advanced biological treatment for industrial waste from the leather industry

The leather industry (tanneries) generates high amounts of toxic wastes, including solid and liquid effluents that are rich in organic matter and mineral content. Vermicomposting was studied as an alternative method of treating the wastes from tanneries. Vermicompost was produced from the following tannery residues: tanned chips of wet-blue leather, sludge from a liquid residue treatment station, and a mixture of both. Five hundred earthworms (Eisenia fetida) were added to each barrel. During the following 135 days the following parameters were evaluated: pH, total organic carbon (TOC), organic matter (OM), cation exchange capacity (CEC), C:N ratio, and chromium content as Cr (III) and Cr (VI). The results for pH, TOC and OM contents showed decreases in their values during the composting process, whereas values for CEC and total nitrogen rose, indicating that the vermicompost reached maturity. For chromium, at 135 days, all values of Cr (VI) were below the detectable level. Therefore, the Cr (VI) content had probably been biologically transformed into Cr (III), confirming the use of this technique as an advanced biological treatment. The study reinforces the idea that vermicomposting could be introduced as an effective technology for the treatment of industrial tannery waste and the production of agricultural inputs.     

Variability of pesticide residues in cauliflower units collected from a field trial and market places in Greece

To estimate the variability of pesticide residue levels present in cauliflower units, a total of 142 samples were collected from a field trial of a cooperative farmer, and 120 samples were collected from different market places in Thessaloniki, Greece. The collected samples were extracted using the quick, easy, cheap, effective, rugged, and safe (QuEChERS) extraction technique, and the residues were determined by liquid chromatography–tandem mass spectrometry. The developed method was validated by evaluating the accuracy, precision, linearity, limit of detection (LOD), and limit of quantification (LOQ). The average recoveries for all the analytes, derived from the data of control samples fortified at 0.01, 0.05, 0.1, and 0.2 mg/kg, ranged from 74 to 110% with a relative standard deviation of ≤8%. The correlation coefficient (R²) was ≥0.997 for all the analytes using matrix-matched calibration standards. The LOD values ranged from 0.001 to 0.003 mg/kg, and the LOQ was determined at 0.01 mg/kg for all the sought analytes. The matrix effect was found to be at a considerable level, especially for cypermethrin and deltamethrin, amounting to +90% and +145%, respectively. For the field samples, the unit-to-unit variability factors (VFs) calculated for cypermethrin and deltamethrin were 2.38 and 2.32, respectively, while the average VF for the market basket samples was 5.11. In the market basket samples, residues of cypermethrin, deltamethrin, chlorpyrifos, and indoxacarb were found at levels ≥LOQ and their respective VFs were 7.12, 5.67, 5.28, and 2.40.     

中和共沉淀—铁氧体法处理含镍、铬废水的实验研究

利用中和共沉淀—铁氧体法处理甘肃某稀有金属生产企业产生的含镍、铬废水,同时对该废水的处理工艺条件进行了实验研究。经测定,废水中Ni 2+质量浓度为50mg/L,Cr(Ⅲ)质量浓度为87mg/L。通过实验得到处理工艺的最佳条件:投料摩尔比(Fe2+/(Ni 2++Cr2O2-7))为9,pH=9,温度为70℃。出水中镍、铬均可达到《污水综合排放标准》(GB 8978—1996)中第一类污染物最高允许排放浓度的要求,为中和共沉淀—铁氧体法处理混合重金属废水的工艺条件研究提供了参考。