Cu 2+ 对分光光度法测定水样中COD的影响

通过测定Cr^3＋、Cr2O7^2-和Cu^2＋吸收曲线及标准水样的COD值,研究了Cu^2＋对分光光度法测定COD的影响。结果表明,可改变吸收波长和量程消除较高质量浓度Cu^2＋对COD测定值产生的明显影响。当水样Cu^2＋质量浓度超过400mg／L时,须将水样稀释后采用低量程法进行测定。     

常温下比色法和滴定法测定化学耗氧量

在强酸性溶液中的催化剂作用下，用重铬酸钾溶液氧化水中的还原性物质，六价铬则还原为三价铬，比色测定，也可在完全反应后，过量的重铬酸钾，以试亚铁灵为指示剂，用硫酸亚铁铵回滴，根据用量计算出化学耗量（ＣＯＤ）。     

高氯、高铵废水COD测定误差及方法适用性分析

以0.25mol/L与0.025mol/L的重铬酸钾法基础方法作比较,通过Cl-干扰影响、Cl-、NH4共存时,NH4的干扰影响及实例分析试验,得知:Cl-对0.25mol/L与0.025mol/L的重铬酸钾法干扰影响基本一致;Cl-浓度≤500mg/L时,Hg2SO4的络合较为理想,Cl-的干扰影响相对较小,COD测定结果相对误差≤5.1%;Cl-、NH+4共存时,NH4对0.25mol/L重铬酸钾法COD测定值有较大的干扰影响,且当NH4浓度≤1500mg/L l时,其COD贡献值与NH4浓度有良好线性关系,并随着Cl-的浓度的增加对应同浓度NH4的贡献值越大;NH4干扰影响是0.25mol/L与0.025mol/L重铬酸钾法COD测定差异的主要原因。在目前还没有有效消除NH4干扰方法的情况下,高氯、高铵、低COD废水样的测定,宜采用0.025mol/L重铬酸钾法。     

氯离子对COD测定的干扰及校正方法的研究

对不同含量范围的氯离子在测定过程中造成的干扰及排除方法作了较系统的研究，采用标准曲线活对氯离子在测定废水COD时的干扰进行校正，用重铬酸钾法测定不同浓度的纯NaCl溶液的COD，将测定结果绘成标准曲线，由水样测定的COD减去标准曲线查得的氯离子校正值，即得水样的真实COD值．该方法简捷、方便，不用剧毒试剂HgSO4，选用于含氯离子500-25000mg／L的COD的测定．     

以MnSO4作催化剂快速测定水中COD

建立了酸性条件下,以MnSO4代替Ag2SO4作催化剂快速测定水中COD的方法.考察了K2Cr2O7用量、MnSO4用量、H2SO4浓度、消解温度、消解时间等因素的影响,确定了最佳试验条件和最佳测定范围.方法精密度和准确度均能满足测定要求,与重铬酸钾法作对比试验,测定结果基本一致.     

废水CODcr测定中硫酸亚铁铵溶液稳定性的试验

废水ＣＯＤ_（ｃｒ）测定中硫酸亚铁铵溶液稳定性的试验周秀华（浙江省平湖市环境监测站３１４２００）目前废水中ＣＯＤ（ｃｒ）值测定普遍采用重铬酸钾滴定法，但由于该方法所用的回滴试剂（硫酸亚铁铵溶液）易受空气、光氧化，导致该溶液浓度下降，在每次使用时，必须?..     

CTL-12型化学需氧量测定仪应用研究

采用CTL-12型化学需氧量测定仪测定CODCr,并与传统的重铬酸钾法比较。实验结果表明,该仪器适用于多种废水、不同浓度CODCr的测定,具有准确、简便、快速等特点。     

重铬酸钾—三氯化钛法测定水中溶解氧

介绍了三氯化钛（ＴｉＣｌ３）与氧反应，以钨酸钠（Ｎａ２ＷＯ４）作指示剂，用重铬酸钾溶液滴定过剩三氯化钛来测定水中溶解氧的方法，本法与碘量法比较，结果表明方法准确，快速，适合于水样中溶解氧的测定。     

重铬酸钾─三氯化钛法测定水中溶解氧

介绍了三氯化钛（ＴｉＣｌ３）与氧反应，以钨酸钠（Ｎａ２ＷＯ４）作指示剂，用重铬酸钾溶液滴定过剩三氯化钛来测定水中溶解氧的方法。本法与碘量法比较，结果表明方法准确、快速，适合于水样中溶解氧的测定     

蒸发浓缩法在地面水COD测定中可行性研究

本文对蒸发浓缩法用于地面水中低浓度ＣＯＤ的测定作了研究,实验结果表明,地面水中ＣＯＤ物质在碱性条件下,能得以定量浓缩,然后采用重铬酸钾法进行测定,所得结果的精密度和准确度良好,若通过蒸发浓缩处理使ＣＯＤ物质浓缩５倍,则可使重铬酸钾法的最低检测限浓度由５０ｍｇ／Ｌ降低到１０ｍｇ／Ｌ,从而使该方法能够适用于地面水水质标准中各类水质ＣＯＤ检测要求。     

水体突发性重金属污染胁迫下斑马鱼的行为反应分析

研究了斑马鱼在不同程度突发性的Zn2＋和Cr6＋胁迫下的行为反应,采用计算机视觉技术量化研究斑马鱼游动行为数据。结果表明,在Zn2＋和Cr6＋的突发性胁迫中,斑马鱼的行为反应快速且敏感,游动行为与污染物种类、质量浓度和暴露时间直接相关,并表现出比较相似的行为变化规律;随着胁迫程度的增加,斑马鱼游动速度的变化幅度增大,反应时间缩短,且其变化曲线符合生物行为的环境压力模型。斑马鱼的行为变化远远提前于生物的病理损伤或死亡,可利用斑马鱼暴露于污染物时的行为变化实现在线水体突发性重金属污染事故的监测预警。     

Reduction and immobilization of chromium(VI) by nano-scale Fe0 particles supported on reproducible PAA/PVDF membrane

A new class of nano-scale Fe0 particles (NZVI) supported on a PAA/PVDF membrane (NZVI-PAA/PVDF) were synthesized and the feasibility of using NZVI-PAA/PVDF for reductive immobilization of Cr(VI) in water was investigated through laboratory batch tests. The results showed that the Cr(VI) removal capacity of NZVI-PAA/PVDF was 181 mg Cr/g Fe at an initial Cr(VI) concentration of 20 mg L(-1) under pH 6.5 +/- 0.1. XPS results showed that Cr(VI) was converted to nontoxic Cr(III). Interfering ions exerted various degrees of impact on NZVI-PAA/PVDF's Cr(VI) removal capacity. Specifically, Ca2+ alone showed the mildest impact while the presence of ions (Mg2+ and HCO3-) exerted the greatest impact. An advantage of NZVI-PAA/PVDF is that the nano-scale Fe0 and resultant particles were combined within a PAA/PVDF membrane, which prevents secondary pollution. Moreover, a piece of PAA/PVDF membrane (4.7 cm diameter) can still support 6.51 mg of nano-scale Fe0 particles after being renewed.     

棕壤吸附-解吸铬影响因素研究

采用室内实验方法,研究了不同铬浓度及不同pH对棕壤吸附-解吸铬的影响,草酸、EDTA和柠檬酸3种有机酸在不同浓度、不同pH条件下对棕壤吸附-解吸铬的影响。结果表明,棕壤对Cr6＋的吸附率随其浓度的增大逐渐增大,并在酸性条件下易于吸附Cr6＋,在碱性条件下易于解吸Cr6＋,低浓度有机酸有利于棕壤对Cr6＋的解吸。EDTA解吸率最大,草酸次之,柠檬酸最小。     

Monitoring the species of arsenic, chromium and nickel in milled coal, bottom ash and fly ash from a pulverized coal-fired power plant in western Canada

The concentration of As, Cr and Ni and their speciation (As3+;5+, Cr3+;6+ and Ni0;2+) in milled coal, bottom ash and ash collected by electrostatic precipitator (ESP) from a coal fired-power plant in western Canada were determined using HGAAS, ICP-AES and XANES. The chemical fractionation of these elements was also determined by a sequential leaching procedure, using deionized water, NH4OAC and HCI as extracting agents. The leachate was analyzed by ICP-AES. Arsenic in the milled coal is mostly associated with organic matter, and 67% of this arsenic is removed by ammonium acetate. This element is totally removed from milled coal after extraction with HCI. Arsenic occurs in both the As3+ and the As5+ oxidation states in the milled coal, while virtually all (>90%) of the arsenic in bottom ash and fly ash appears to be in the less toxic arsenate (As5+) form. Both Ni and Cr in the milled coal are extracted by HCI, indicating that water can mobilize Ni and Cr in an acidic environment. The chromium is leached by water from fly ash as a result of the high pH of the water, which is induced during the leaching. Ammonium acetate removes Ni from bottom ash through an ion exchange process. Chromium in milled coal is present entirely as Cr3+, which is an essential human trace nutrient. The Cr speciation in bottom ash is a more accentuated version of the milled coal and consists mostly of the Cr3+ species. Chromium in fly ash is mostly Cr3+, with significant contamination by stainless-steel from the installation itself.     

原子吸收法测定废水中的铬（Ⅵ）

在pH<1的溶液中,用甲基异丁酮(MIBK)与磷酸三丁酯(TBP)混合作为萃取剂,萃取废水中的铬时,六价铬的分配比为108.6,而三价铬几乎不被萃取。用原子吸收分光光度计测定有机相中的六价铬具有很好的选择性,且干扰少,灵敏度高。工作曲线的最佳浓度范围是:0.04～4.00mg/L。     

重金属离子对斜生栅列藻毒性的研究

应用斜生栅列藻作为生物指示物,对16种重金属化合物的单一毒性进行毒性评价,并分别从微观和宏观角度分析了重金属的致毒机理。实验结果表明:它们的毒性大小顺序为Ag+Cd2+Cu2+Zn2+Sr2+Pb2+Hg2+Sn4+Al3+Cr+Ni2+Mn2+Ba2+Fe3+Co2+Li+。     

空气-乙炔火焰原子吸收法测铬时的干扰及消除

对空气-乙炔火焰原子吸收法测铬(Cr)时共存元素对其测定结果的干扰进行研究。结果表明,当ρ(共存元素)/ρ(Cr)100时,Mg、Co、Al、V、Ni、Fe、Na、Ca对Cr测定有影响,而K、Mn、Zn、Mo、Pb、Si、Cu均不影响Cr的测定;当ρ(共存元素)/ρ(Cr)为10和30时,加入1%HNO_3和2%NH_4Cl可消除干扰;当ρ(共存元素)/ρ(Cr)30时,加入5%HCl和超过1%的NH_4Cl可消除干扰;5%HCl作为介质消除Cr测定干扰的效果要优于1%HNO_3介质。     

Accumulation of heavy metals in Spinacia oleracea irrigated with paper mill effluent and sewage

The present study on heavy metal contamination in soil and their accumulation in edible part (leaves) and roots of Spinacia oleracea (Spinach) on irrigation with paper mill effluent (PME)/sewage revealed that there was significant increase in the nickel (Ni, +227.17 %) content of the soil irrigated with PME, whereas in the soil irrigated with sewage chromium (Cr, +274.84 %), iron (Fe, +149.56 %), and cadmium (Cd, +133.39 %), contents were increased appreciably. The value of enrichment factor (EF) for Ni (3.27) indicated moderate enrichment in PME-irrigated soil. The EF of Fe, zinc (Zn), Cd, and Cr were <2 in PME effluent-irrigated soil which showed deficiency of minimal enrichment. In sewage irrigated soil, EF value for Cr, Fe, and Cd indicated moderate enrichment, while the values for Zn and Ni indicated deficiency of minimal enrichment. Among various metallic concentrations, the maximum concentration of Fe was observed in leaves (400.12?±?11.47 mg/kg) and root (301.41?±?13.14 mg/kg) of S. oleracea after irrigation with PME, whereas the maximum concentrations of Fe was found in leaves (400.49?±?5.97 mg/kg) and root (363.94?±?11.37 mg/kg) of S. oleracea after irrigation with sewage for 60 days. The bioaccumulation factor value was found maximum for Cd (2.23) in the plants irrigated with PME while that of Fe (0.90) in the plants irrigated with sewage. The undiluted use of PME/sewage for irrigation increased the concentration of Cr, Cd, Zn, Ni, and Fe metals which were accumulated in S. oleracea, posing a potential threat to human health from this practice of irrigation.     

Ferti-irrigational impact of sugar mill effluent on agronomical characteristics of Phaseolus vulgaris (L.) in two seasons

Ferti-irrigation response of 5, 10, 25, 50, 75, and 100 % concentrations of the sugar mill effluent (SME) on French bean (Phaseolus vulgaris L., cv. Annapurna) in the rainy and summer seasons was investigated. The fertigant concentrations produced significant (P?+), potassium (K⁺), calcium (Ca²⁺), magnesium (Mg²⁺), total Kjeldahl nitrogen (TKN), phosphate (PO₄ ^3?), sulfate (SO₄ ^2?), ferrous (Fe²⁺), cadmium (Cd), chromium (Cr), copper (Cu), manganese (Mn), and zinc (Zn), in both seasons. The contents of Cr, Cu, Mn, and Zn except Cd were found to be below the maximum levels permitted for soils in India. The agronomic performance of P. vulgaris was gradually increased at lower concentrations, i.e., from 5 to 25 %, and decreased at higher concentrations, i.e., from 50 to 100 %, of the SME in both seasons when compared to controls. The accumulations of heavy metals were increased in the soil and P. vulgaris from 5 to 100 % concentrations of the SME in both seasons. The contents of Cu, Mn, and Zn except Cd and Cr were noted under the permissible limit of Food and Agriculture Organization (FAO)/World Health Organization (WHO) standards. Most contents of biochemical components like crude proteins, crude fiber, and total carbohydrates were found with 25 % concentration of the SME in both seasons. The contamination factor (Cf) of various metals was in the order of Cd > Cr > Zn > Mn > Cu for soil and Mn > Zn > Cu > Cr > Cd for P. vulgaris in both seasons after fertigation with SME. Therefore, the SME can be used to improve the soil fertility and yield of P. vulgaris after appropriate dilution.     

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.