ICP-AES法测定土壤中铜、钒、镍和铬

在HNO3-H2O2-HF体系中微波消解土壤样品，用电感耦合等离子发射光谱法测定土壤中的铜、钒、镍、铬，设定了最佳的样品处理条件和仪器条件，该方法测定铜、钒、镍、铬检出限分别为0．01mg／kg、0．05mg／kg、0．5mg／kg、0．10mg／kg，回收率为98．4％～102．0％，方法简便、准确。     

衡山PM_（2.5）中痕量金属元素的分析

建立了微波消解-电感耦合等离子体质谱法同时测定PM2.5中12种痕量金属元素的方法。对不同消解体系进行了讨论,确定采用HNO3＋H2O2消解体系。方法检出限在0.01～6.4 ng/m3之间,精密度为0.5%～8.9%,加标回收率在69.2%～92.6%之间。应用该方法测定了衡山PM2.5中痕量金属元素的含量,讨论了痕量元素的浓度分布特征,对各元素进行了相关性分析,并应用富集因子法对来源进行了分析。     

基于微波消解的ICP-MS/ICP-OES方法测定环境土壤中总磷

基于HNO3-HF-H2O2消解体系进行微波消解后,利用ICP-MS/ICP-OES进行环境土壤中总磷测试。通过优化仪器参数及采取干扰校正措施,两台仪器校准曲线r均大于0.999,其中ICP-MS方法检出限0.05μg/g,RSD在0.67%～1.22%之间,加标回收率106%～114%;ICP-OES方法检出限在5μg/g,RSD在0.29%～0.61%之间,加标回收率105%～108%。用GSS-13和GSS-10标准样品验证,两台仪器的磷测定值与标准值吻合,微波消解ICP-MS/ICP-OES方法可以满足环境土壤中总磷分析的要求。     

氢化物发生原子荧光法测定钻井废水中的铅

目前测定铅的分析方法主要有分光光度法、阳极溶出伏安法、示波极谱法、原子吸收法等。针对比色法灵敏度低,试剂不稳定;电化学法干扰严重;而原子吸收法,线性范围窄,样品用量大等问题,江苏油田采用氢化物发生原子荧光法测定钻井废水中的铅。样品经HNO3-HClO4消解,3％～4％KBH4还原,以0.8％～1.5％的HCl为介质,加入10％K3Fe(CN)6和2％H2C2O4基体改进剂,用原子荧光法连续测定钻井废水中的铅。铅的检测限为0.61ng/mL,回收率为87.4％～146％,变异系数＜4.2％。该方法操作简单,灵敏度高。     

紫外光催化氧化-原子吸收分光光度法测定垃圾渗滤液中重金属的研究

本文采用二氧化钛为催化剂，通过使用光催化氧化的消解方法对垃圾渗滤液样品进行前处理，再用原子吸收分光光度法测定垃圾渗滤液中的重金属，并与常用消解方法进行对比，探讨了紫外光照射时间、紫外灯功率、H2O2的用量等因素对消解效果所产生的影响，选取了消解垃圾渗滤液的最佳条件，讨论了方法的准确度与精密度。     

油田含油污泥中重金属元素测定的前处理方法研究

通过试验对比分析，研究了油田含油污泥中8种重金属测定的前处理方法。得出适用于油田含油污泥样品中不同重金属元素检测时的前处理方法。分析结果表明，对检测Zn、Cd元素，HNO₃-H₂O₂法、HCl-H₂O₂法、王水法三种前处理消解效果较好，其中HCl-H₂O₂法消解效果最佳；对测定Ni、Cr元素，固废法为最佳前处理方法，对测定Ba元素，HNO₃-H₂O₂-HClO₄法消解效果最佳；对测定Be元素，固废法、王水-H₂O₂法、HNO₃-H₂O₂-HClO₄法、HCl-H₂O₂法、王水法消解效果相同；对检测Pb元素，王水-H₂O₂法消解效果最...     

微波萃取肉类样品中的多氯联苯方法研究

用丙酮和正己烷（1＋1）的混合溶剂做萃取剂，采用微波萃取的方法提取动物肉类中的9个多氯联苯（PCBs）单体，通过弗罗里硅土和氧化铝净化后，在带ECD检测器的气相色谱上测定。取样量为2g时，多氯联苯（PCBs）在GC—ECD上响应的线性范围为11～100ng／g，研究的样品加标测定范围为11—500ng／g，检出限从5．3—13．3ng／g，平均加标回收率在98．7％-118％。     

应用三种不同处理方法消解土壤的研究

本文采用3种不同的消解方法对环境土壤标准物质ESS-2和ESS-3进行处理,火焰原子分光光度法分别测定其中铜(Cu)、锌(Zn)元素的含量.3种消解方法为:电热板消解法、微波消解法和全自动消解法.分析测定结果探讨这3种消解方法的优缺点,以期获得最经济实效的消解手段.实验证明:微波消解法操作简便快捷、赶酸时间短、无污粢、准确度高、精密度好,因此提高了工作效率.     

TOA-MIBK萃取火焰原子吸收法同时测定土壤及蔬菜中铅镉

用氢氟酸、硝酸、高氯酸消化土壤样品,干灰化法消解蔬菜样品,用相对TOA-MIBK系统萃取,火焰原子吸收光谱法在同一条件下测定土壤、蔬菜中的铅、镉。在选定条件下,测得土壤铅、镉的相对标准偏差分别为2．3％～4．4％和3．0％～4.3％,蔬菜铅、镉的相对标准偏差分别为2．9％～4．5％和2．6％～4．5％;土壤铅、镉的回收率分别为96％～104％和95％～101％,蔬菜铅、镉的回收率分别为93％～102％92％104％。由测定结果得出离公路越近,蔬菜、土壤铅、镉含量越高。     

省沽油中硒含量及其测定方法研究

采用消化液硝酸／高氯酸消解法、硝酸-硫酸消解法和微波消解方法消化省沽油，用原子吸收分光光度法测定硒（Se）含量。比较了3种消解方法在测定省沽油中的硒含量。发现微波消解法测定野生省沽油（干菜）中Se含量准确性好、时间段效率高、对环境污染少、操作简单。     

Optimization of the electrocoagulation process for the removal of copper, lead and cadmium in natural waters and simulated wastewater

Chemical, electrochemical and flow variables were optimized to examine the effectiveness of the electrocoagulation process for the removal of copper, lead and cadmium. The electrochemical process, which uses electrodes of commercial laminate steel, was applied to simulated wastewater containing 12 mg dm(-3) of copper, 4 mg dm(-3) of lead and 4 mg dm(-3) of cadmium. The optimum conditions for the process were identified as pH=7, flow rate=6.3 cm(3) min(-1) and a current density between 31 and 54 A m(-2). When the electrode geometric area and time of electrolysis reached critical values, the copper removal reached a maximum value of 80%. A linear relationship was identified between the current density and the mass of generated sludge. In addition, a linear relationship was found between specific energy consumption and current density. The results of this investigation provide important data for the development of an industrial-scale electrolytic reactor.     

Metals distribution and interactions in tissues of shrews (Sorex spp.) from copper- and zinc-contaminated areas in Poland

To assess the risk from heavy metal accumulation to insectivorous species exposed to different pollutants, shrews [Sorex araneus (Linnaeus 1758) and Sorex minutus (Linnaeus 1766)] were collected in the Olkuski Ore Region (OOR; a Zn and Cd smelter area), Legnicko-G?ogowski Copper Mine Region (LGCR; a copper ore-mining area), and Bia?owieza Forest (BF; a control area). A few sites were chosen in each region and a total of 57 animals were collected from them. The liver and kidneys were dissected from the animals, dried, and digested in a 4:1 mixture of HNO3 (nitric acid) and HClO4 (perchloric acid). Cadmium, lead, zinc, copper, and iron were determined in the samples by flame or flameless atomic absorption spectrometry. The interactions between toxic and essential metals were calculated for each tissue. The data showed that accumulation of metals by insectivores is high; shrews accumulated much higher amounts of cadmium and lead than bank voles, studied by other researchers, from the same areas. The expected high tissue accumulation of copper at LGCR and zinc at OOR was not seen, but the levels of both elements were higher in the tissues of shrews from OOR than from LGCR. The lowest copper concentrations were in the tissues of shrews from BF. The highest cadmium and lead concentrations were found in the tissues of shrews from OOR. Some significant correlations were found between the tissue concentrations of xenobiotic and essential metals (e.g., between cadmium and zinc and between lead and iron).     

Cadmium in aquatic microcosms: Implications for screening the ecological effects of toxic substances

A two-phase set of experiments was conducted to address some of the problems inherent in ecological screening of toxic substances in aquatic microcosms. Phase I was a 4×4 factorial experiment dealing with the interactive effects of cadmium and nutrients in static microcosms. Phase II was a 2×4 factorial experiment using flowthrough microcosms to study temporal aspects of system behavior in response to nutrient loading and chronic versus acute cadmium perturbations. Nutrient enrichment resulted in increased biomass and metabolic activity in both static and flowthrough microcosms. Cadmium treatments generally resulted in a decrease in abundance of grazing crustaceans and a subsequent increase in community respiration, suggesting a change in community structure from a grazing to a detritus food chain. Of the variables measured, community metabolism, community composition, and output/input ratios of nitrate-nitrogen were the most useful indicators of system response to cadmium. Nutrient enrichment significantly influenced cadmium effects with respect to most of the variables measured; high levels of enrichment reduced the effects of cadmium. For screening the ecological effects of toxic chemicals, a series of experiments is proposed, including 1) relatively simple static microcosms, 2) flow through microcosms, and 3) more detailed but selective studies in microcosms derived from specific ecosystems. Each step yields increasingly more information and serves as a guide for subsequent experiments; in addition, each step more closely approximates natural ecosystems.     

Transport of cadmium and assessment of phytotoxicity after electrokinetic remediation

The use of ethylene diamine tetraacetic acid (EDTA) on the electrokinetic removal of cadmium-contaminated soil was evaluated. A total of four different tests were conducted using EDTA as a washing solution as well as a purging solution at the electrode compartments. The efficiency of electrokinetic extraction was significantly influenced by the pH of the soil medium. The results show that EDTA was effective in desorbing cadmium at a high pH, with Cd-EDTA(-) anion complexes migrating toward the anode. At low pH values near the anode area, cadmium existed as Cd(2+), migrating toward the cathode. Such contradicting directions of cadmium have resulted in its detrimental removal from the soil cell. However, accumulation of cadmium near the cathode was observed at the end of the tests due to the dominating low pH in the soil cell. The phytotoxicity after the electrokinetic process was investigated using Sorghum saccharatum, Lepidium sativum and Sinapis alba plants. The germination index was a major endpoint estimated by measuring seed germination and shoot elongation. The results obtained show that the phytotoxicity was increased after electrokinetic extraction. Despite, the extensive cadmium removal from two-thirds of the cell, the low pH of the soil was the principal parameter exhibiting the phytotoxicity.     

Adsorption of nutrients and cadmium by different minerals: experimental studies and modelling

This work analyses cadmium sorption by natural vermiculite, zeolite, and pumice, which have been recently considered for their potential use in remediation of contaminated soils. Batch experiments were performed to investigate the interactions between the mineral surfaces and the main nutritive cations of Hoagland solution. In addition to their ameliorative effect of reducing metal mobility, these minerals are able to interact to different extents with various components of the nutrient solution and can change the availability of essential nutrients in solution. Therefore, the minerals were also exposed to a range of cadmium doses to compare their different affinities for this element and to analyse the cadmium–nutrient interactions. The results showed that the nutrient solution composition was significantly modified by contact with zeolite and vermiculite, and to a minor extent with pumice. The ionic equilibrium between the solid and aqueous phases was attained at several time points depending on the cation. Ammonium and potassium ions were almost entirely absorbed by zeolite, while in vermiculite endogenous magnesium ions were exchanged with the liquid phase calcium ions. The amount of cadmium adsorbed on mineral surfaces equilibrated with the nutrient solution showed the following sequence zeolite>vermiculite>pumice, and the cation concentrations of the fluid phase were sensitive to cadmium addition.     

Cadmium—Towards a rational use of a toxic element

Because of its toxicity, cadmium creates an environmental problem as well as a health hazard for exposed workers. Most cadmium emissions arise from the intentional use of the element. It is therefore mandatory to reduce cadmium consumption to the lowest possible level. Cadmium pigments, mainly used in plastic processing, can be replaced in all applications where the processing temperature does not exceed 300°C. Newly developed polyvinyl chloride stabilizers promise to be an excellent substitute for cadmium stabilizers in even the most demanding applications. Cadmium plating, still extensively used in the United States and the West Germany, has been virtually abandoned in Japan. Improved lead acid batteries are replacing vented nickel cadmium batteries because of their cost effectiveness. While in these applications cadmium use is declining, more and more cadmium is needed for the manufacturing of sealed nickel cadmium batteries. These relatively small electrochemical cells are used mainly by individual consumers. Here cadmium can only be replaced in some marginal applications. The high cadmium content of these batteries (up to 22%) makes them a good candidate for recycling of the heavy metal.     

广东省部分基地蔬菜重金属污染评价

通过对来源于广东省516个蔬菜种植基地18种蔬菜品种1 465个样品中铅、镉含量的检测分析,结果表明：蕹菜品种铅平均含量最高（0.11mg·kg^-1）,西洋菜镉平均含量最高（0.060mg·kg^-1）;总样品铅检测合格率97.0%,镉检测合格率98.9%;所检蔬菜品种的铅、镉平均污染指数均小于0.7。表明广东省各生产基地的蔬菜重金属安全状况总体较好,处于优良水平。     

EVALUATION OF PHILODINA ACUTICORNIS (ROTIFERA) AS A BIOASSAY ORGANISM FOR HEAVY METALS1

ABSTRACT: A technique for using the rotifer Philodina acuticornis as a bioassay organism is described. The rotifer was exposed to a range of concentrations for each of 14 toxicants. The effects of the heavy metals cadmium, chromium, cobalt, copper, lead, mercury, nickel, silver and zinc were studied. Based upon 96 hours exposure in soft water the sensitivity of the rotifer to the metals from the most toxic to least toxic was: cadmium, mercury and copper, zinc, silver, nickel (chloride), chromium, nickel (sulfate), lead and colbalt. In hard water with 96 hours exposure the most to least toxic respectively were: cadmium, copper, mercury, chromium and lead. The 48 hour EC₅₀ value suggests that zinc will follow mercury in relative toxicity when Philodina is tested in hard water. In a comparison of the toxicity of the chloride and sulfate salts of cadmium, nickel and zinc in soft water cadmium sulfate and zinc sulfate were more toxic after 96 hours; nickelous chloride was more toxic than nickelous sulfate. Increased water hardness decreased the toxicity of the heavy metals studied. The results suggest that this rotifer may be more sensitive than the bluegill sunfish to the salts of cadmium, copper, nickel, zinc and chromium and less sensitive to lead. Data for cobalt, silver and mercury were not available. Philodina was extremely tolerant of ammonium chloride and phenol. The feasibility and economics of using an inexpensive, readily cultured and available organism such as Philodina acuticornis as a bioassay organism were discussed.     

Contamination time effect on lead and cadmium fractionation in a tropical coastal clay

The capability of a tropical coastal clay to immobilize lead (Pb) and cadmium (Cd) was investigated in laboratory batch sorption tests conducted under acidic, neutral, and slightly alkaline conditions. The contact time was extended to 65 d. The distribution of Pb and Cd among various sorbed phases was examined using a sequential extraction technique. The sorbed phases were fractionated into the exchangeable, carbonate, reducible, organic, and residual fractions. There were only small changes in the total Pb and Cd sorption beyond a 1-d sorption period. The metal fractionation results show that the amount of Pb and Cd in various fractions changed with sorption time, and the changes were pH-dependent. These changes could be attributed to mineral dissolution and transformation or redistribution of the sorbed phases. Transformation of the sorbed phases resulted in increasing Pb and Cd retention in the more persistent fractions with time, at the expense of reductions in the loosely bound fractions. Nevertheless, Pb and Cd fractionation in the solid phase appeared to reach equilibrium within the 65-d sorption period. These Pb and Cd fractionation results reflect the effect of contamination time on the heavy metal lability and bioavailability in the subsurface environment.     

某区域内矿区土壤重金属污染与生态风险评价

探究区域内矿区土壤重金属变化并对其进行污染评价,旨在为该区域环境保护及污染治理提供一定的理论依据,以期实现矿山地质环境保护与矿产资源开发并行的矿业绿色发展。以铅、锌、镉、砷含量为评价指标,结合《土壤环境质量标准》(GB 15618—2018),采用重金属单因子污染指数法与内梅罗综合污染指数法进行重金属污染评价,并对该区域矿区潜在生态风险作出评定。结果表明,A矿区土壤各重金属含量的变异系数为149.05%~211.42%,B矿区土壤各重金属含量变异系数为60.88%~118.58%;A矿区土壤重金属均出现超标现象,其中铅、锌和镉含量超标较为严重,超标率在72%以上,而砷含量超标现象则相对较轻,超标率为36.36%;B矿区土壤铅和锌含量均未出现超标,超标率为0,而砷和镉含量则出现不同程度的超标,其中砷含量超标率为92.31%,镉含量超标率为65.38%;两个矿区土壤各重金属含量均超背景值的现象,超背景值比例为42.31%~100.00%。A矿区土壤以铅、锌和镉污染为主,而B矿区土壤中砷和镉的污染较为严重。两个矿区土壤重金属综合污染指数均属重度污染,A矿区生态风险综合指数为很强生态风险危害,而B矿区为中等生态风险危害。