废水中微量Cr^6＋测定中的试样前处理

采用离子交换树脂预处理工业废水方法测定微量Ｃｒ＾６＋，排除了Ｃｒ＾３＋、Ｆｅ＾３＋、Ｈｇ＾２＋等阳离子干扰，减除水中浊度、色度、免去冗长预处理手续，使原方法简便易行，回收率达９０％以上。     

甘肃省饮用水中几种有毒有在元素的调查分析

通过对甘肃省饮用水中Ｃｄ，Ｐｂ，Ｃｒ＾＋６，Ｂｅ，Ａｓ，Ｈｇ，Ｕ等元素含量的分析调查，表明全省饮用水除个别项目超标外，基本没有受到有毒，有害元素的污染，水质符合国家饮用水卫生标准。     

测定甲基托布津的分光光度法的研究

用Ｃｕ＾２＋和甲基托布津在氨碱性条件下作用产生沉淀,离心分离未反应的Ｃｒ＾２＋,经ＣＯ显色剂在柠檬酸缓冲液中显色后,测定溶液中的Ｃｒ＾２＋浓度可间接求得甲基托布律的含量。此方法简便快捷,且可进行微量测定。用本方法与络合滴定法做对照试验。结果能很好的符合。     

测定地面水中Cr~(6+)的回收率问题的探讨

测定地面水中Ｃｒ６＋的回收率问题的探讨马文英张占银（河北邢台市环境保护局,邢台０５４０００）色度很深的水样,用锌盐沉淀分离法进行预处理脱色后还应消除氧化性物质方可进行Ｃ６＋ｒ测定,这是绝对不可忽视的一个关键。消除氧化性物质的处理步骤：水样置于１５０ｍ...     

催化动力学光度法测定水体中痕量钒（Ⅴ）

在柠檬酸介质中，Ｖ＾５＋对ＫＢｒＯ３氧化甲基兰的反应有强烈的催化作用。研究了其催化动力学条件，建立了痕量Ｖ＾５＋的测定方法，方法检出限为４ｎｇ／Ｌ，线性范围为０￣２００ｎｇ／２５ｍｌ，对环境水样进行了精密度试验和加标回收实验，相对偏差为９％加标回收率为９０．６％￣９８．８％。     

离子色谱法测定水中主要阳离子

报导了水中阳离子Ｌｉ＾＋，Ｎａ＾＋，Ｋ＾＋，Ｃａ＾２＋〉Ｍｇ＾２＋的离子色谱分析及其分析精密度，准确性和线性范围。与阴离子组分同时测定用于水中离子总量的分析，获得满意结果。     

兰州市生物样品放射性核素水平及地域性分布研究

本文报道了兰州市生物样品中天然及人工放射性核素＾２３８Ｕ，＾２３２Ｔｈ，＾２２６Ｒａ，＾４０Ｋ，＾９０Ｓｒ，＾１３７Ｃｓ和总α，总β水平，研究了它们在各区（县）分布情况，为制定和修订我国及地方《食品中放射性物质限制浓度标准》提供实际资料。     

石河子市地下水环境背景值

采集并测定了石河子市１９个地下水背景水样，分别确定了该市潜水和承压—自流水中Ｋ＋、Ｎａ＋、Ｃａ２＋、Ｍｇ２＋、Ｃｌ－、ＳＯ、ＨＣＯ、ＮＯ、Ｆ－、总硬度、矿化度、可溶性ＳｉＯ２、ＣＯＤ、ｐＨ、Ｃｕ、Ｐｂ、Ｚｎ、Ｃｄ、Ｍｎ、Ｖ、Ｌｉ、Ｍｏ、Ｓｅ、Ｈｇ、Ｉ、Ａｓ、Ｃｒ＋５、Ｃ６Ｈ５ＯＨ、ＣＮ－、ＡＢＳ的环境背景值．     

停流──诱导动力学光度法测定微量钒

Ｃｒ（Ⅳ）－Ⅰ－淀粉体系的氧化还原反应可被Ｃｒ（Ⅳ）－Ｖ（Ⅳ）反应所诱导,本文据此提出了一种测定微量钒（Ⅳ）的停流－诱导动力学光度法,并建立了测定最佳条件。常见离子中,除Ｆｅ２＋,Ｔｒ１＋,Ｓｅ４＋,Ａｓ３＋以外,大部分不干扰测定。本法测定钒（Ⅳ）的线性范围为０～１．８μｇ／ｍｌ;测定了土壤中微量钒,六次测定的ＲＳＤ＝２．４５％。     

从CODcr废液中回收银及硫酸银

从ＣＯＤｃｒ废液中回收银及硫酸银刘艳，张向东（石河子市环境监测站８３２０００）用重铬酸钾法测定ＣＯＤＣｒ需加入硫酸银作催化剂。每测定一个水样需消耗约０．３ｇ硫酸银，每升废液中约含２．１ｇ硫酸银。含Ａｇ＋废水排入城市下水道，不仅污染环境，也是经济损失。...     

基于改进火焰原子吸收光谱的土壤六价铬分析

针对分离和萃取环节,对火焰原子吸收光谱测定土壤中六价铬的方法加以改进。采用聚合氯化铝为絮凝剂、异戊醇为萃取剂,使三价铬和六价铬有效分离,并减少了测试干扰。考察了聚铝试剂用量和萃取液振荡时间对测定的影响,并将该方法与EPA 3060A方法和未改进的火焰原子吸收光谱法比较,表明改进后的方法能用于土壤中六价铬的测定。     

基于智能手机比色测定水环境中的六价铬

在酸性条件下,水样中的六价铬能够和显色剂二苯碳酰二肼反应生成紫红色络合物,该络合物溶液用自制的数字图像比色装置测定颜色值实现六价铬的现场快速检测.该方法在0.05 mg/L～1.00 mg/L范围内线性良好,方法检出限为0.02 mg/L,标准溶液10次测定结果的RSD为1.6％ ～7.9％,实际水样加标回收率为94....     

Determination and evaluation of hexavalent chromium in power plant coal combustion by-products and cost-effective environmental remediation solutions using acid mine drainage

The chromium species leaching from a coal combustion fly ash landfill has been characterized as well as a novel approach to treat leachates rich in hexavalent chromium, Cr(VI), by using another natural waste by-product, acid mine drainage (AMD), has been investigated during this study. It is observed that as much as 8% (approximately 10 microg g(-1) in fly ash) of total chromium is converted to the Cr(VI) species during oxidative combustion of coal and remains in the resulting ash as a stable species, however, it is significantly mobile in water based leaching. Approximately 1.23 +/- 0.01 microg g(-1) of Cr(VI) was found in the landfill leachate from permanent deposits of aged fly ash. This study also confirmed the use of AMD, which often is in close proximity to coal combustion by-product landfills, is an extremely effective and economical remediation option for the elimination of hexavalent chromium in fly ash generated leachate. Speciated isotope dilution mass spectrometry (SIDMS), as described in EPA Method 6800, was used to analytically evaluate and validate the field application of the ferrous iron and chromate chemistry in the remediation of Cr(VI) runoff.     

流动注射分光光度法测定水中六价铬的研究

研究建立了测定水中六价铬的流动注射光度分析方法,探讨了利用抗坏血酸的还原性扣除水样中轻度色度或浊度干扰的可行性.本方法线性关系好,检出限低,精密度和准确度高,对地表水、地下水、生活污水、工业废水等实样的测定获得了令人满意的结果.与传统的二苯基碳酰二肼分光光度法相比,具有方法简单、灵敏度高、分析速度快等优点,适用于环境监测的分析工作.     

铬盐工业项目特征污染物的监测与数据问题分析

对铬及其化合物工业项目排放废气中特征污染物的监测方法和评价标准问题进行探讨,提出了验收监测应参考《大气污染物综合排放标准》(GB 16297—1996)的建议;通过对监测数据的合理性和逻辑性分析,提出了现场监测和数据审核的注意事项,应严格监控工况,并详细记录关键设备运行参数;提出应把废气中六价铬作为特征污染物控制指标,并结合新颁布的《环境空气质量标准》(GB 3095—2012)中对六价铬的要求,确定合理的排放限值,并研究适合的配套监测方法,为后续铬及其化合物工业污染物排放标准以及特征污染物监测方法的制修订提供技术依据。     

Preconcentration and speciation of Cr(III) and Cr(VI) in water and soil samples by spectrometric detection via use of nanosized alumina-coated magnetite solid phase

A novel nanomaterial has been developed for speciation of Cr(III) and Cr(VI) in water and soil samples. In this study, a new type of alumina-coated magnetite nanoparticles (Fe₃O₄/Al₂O₃ NPs) modified by the surfactant Triton X-114 has been successfully synthesized and used in magnetic mixed hemimicelles solid-phase extraction procedure. The procedure was based on the reaction of chromium(III) with 1-(2-pyridilazo)-2-naphtol as a ligand, yielding a complex, which was entrapped “in situ” in the surfactant hemimicelles. The concentration of chromium(III) was determined using flame atomic absorption spectrometry. After reduction of Cr(VI) to Cr(III) by ascorbic acid, the system was applied to the total chromium. Cr(VI) was then calculated as the difference between the total Cr and the Cr(III) content. This method can also be used for complicated matrices such as soil samples without any special pretreatment. Under the optimum conditions of parameters, the recoveries of Cr(III) by analyzing the spiked water and soil samples were between 98.6 and 100.8 % and between 96.5 and 100.7 %, respectively. Detection limits of Cr(III) were between 1.4 and 3.6 ng?mL^?1 for water samples and 5.6 ng?mg^?1 for soil samples.     

Sampling and analysis considerations for the determination of hexavalent chromium in workplace air

Airborne hexavalent chromium (Cr[VI]) is a known human respiratory carcinogen and allergen. Workers in a variety of industries may be exposed to airborne hexavalent chromium, with exposures frequently occurring via inhalation and/or dermal contact. Analytical methods for the measurement of Cr(VI) compounds in workplace samples, rather than for the determination of total elemental chromium in workplace air, are often desired because exposure limit values for Cr(VI) compounds are much lower than for total Cr. For years, sampling and analytical test methods for airborne Cr(VI) have been investigated so as to provide means for occupational exposure assessment to this highly toxic species. Inter-conversion of trivalent chromium (Cr[III]) and Cr(VI) can sometimes occur during sampling and sample preparation, and efforts to minimize unwanted redox reactions involving these chromium valences have been sought. Because of differences in toxicity, there is also interest in the ability to differentiate between water-soluble and insoluble forms of Cr(VI), and procedures that provide solubility information concerning Cr(VI) compounds have been developed. This paper reviews the state of the art concerning the measurement of airborne Cr(VI) compounds in workplace aerosols and related samples.     

Effect of Trivalent and Hexavalent Chromium on Carbohydrate Metabolism of a Freshwater Field Crab, Barytelphusa guerini

The in vivo toxic impact of chromium in its two forms(trivalent and hexavalent) on glycogen metabolism in the tissuesof freshwater field crab Barytelphusa guerini was studied.In a sublethal long-term exposure of 30, 60 and 90 days, thedepletion of glycogen and glucose levels reflected in theactivity of glycogenphosphorylases `a' and `ab'. A tissuespecific and time-dependent variation in tissue glucose reservesparelleled the progressive accumulation of haemolymph sugars.Trivalent and hexavalent chromium induced alterations in metabolite levels and in enzyme activities in the tissues. Themagnitude of responses were found more in the hexavalent formthan in trivalent form.     

Evaluation of Early Life Stage Fall Chinook Salmon Exposed to Hexavalent Chromium from a Contaminated Groundwater Source

We conducted a laboratory evaluation to assess the risk to early life stage (i.e., eyed egg to swim up) fall Chinook salmon (Oncorhynchus tshawytscha) for exposure to hexavalent chromium from a contaminated groundwater source. Local populations of fall Chinook salmon were exposed to Hanford Site source groundwater that was diluted with Columbia River water. Specific endpoints included survival, development rate, and growth. Tissue burdens of fish were also measured to estimate uptake and elimination rates of chromium. Survival, development, and growth of early life stage fall Chinook salmon were not adversely affected by extended exposures (i.e., 98 day) to hexavalent chromium ranging from 0.79 to 260 μg/l. Survival for all treatment levels and controls exceeded 98% at termination of the test. In addition, there were no differences among the mean lengths and weights of fish among all treatment groups. Whole-body concentrations of chromium in early life stage fall Chinook salmon had a typical dose-response pattern; i.e., those subjected to highest exposure concentrations and longest exposure intervals had higher tissue concentrations. Given the spatial extent of chromium concentrations at the Hanford Site, and the dynamics of the groundwater–river water interface, the current cleanup criterion of 10 μg/l chromium appear adequate to protect early life stage fall Chinook salmon. These findings, together with previous research indicate low risk to these populations.     

Unanticipated potential cancer risk near metal recycling facilities

Metal recycling is an important growing industry. Prior to this study, area sources consisting of metal recycling facilities fell in a category of limited regulatory scrutiny because of assumed low levels of annual emissions. Initiating with community complaints of nuisance from smoke, dust and odor, the Houston Department of Health and Human Services (HDHHS) began a monitoring program outside metal recycler facilities and found metal particulates in outdoor ambient air at levels which could pose a carcinogenic human health risk. In a study of five similar metal recycler facilities which used a torch cutting process, air downwind and outside the facility was sampled for eight hours between 6 and 10 times each over 18 months using a mobile laboratory. Ten background locations were also sampled. Iron, manganese, copper, chromium, nickel, lead, cobalt, cadmium and mercury were detected downwind of the metal recyclers at frequencies ranging from 100% of the time for iron to 2% of the time for mercury. Of these metals, chromium, nickel, lead, cobalt, cadmium and mercury were not detected in any sample in the background. Two pairs of samples were analyzed for total chromium and hexavalent chromium to establish a ratio of the fraction of hexavalent chromium in total chromium. This fraction was used to estimate hexavalent chromium at all locations. The carcinogenic risk posed to a residential receptor from metal particulate matter concentrations in the ambient air attributed to the metal recyclers was estimated from each of the five facilities in an effort to rank the importance of this source and inform the need for further investigation. The total risk from these area sources ranged from an increased cancer risk of 1 in 1,000,000 to 6 in 10,000 using the 95th upper confidence limit of the mean of the carcinogenic metal particulate matter concentration, assuming the point of the exposure is the sample location for a residential receptor after accounting for wind direction and the number of shifts that could operate a year. Further study is warranted to better understand the metal air pollution levels in the community and if necessary, to evaluate the feasibility of emission controls and identify operational improvements and best management practices for this industry.This research adds two new aspects to the literature: identification of types and magnitude of metal particulate matter air pollutants associated with a previously unrecognized area source, metal recyclers and their potential risk to health.