催化光度法测定水中痕量亚硝酸根

基于亚硝酸根对溴酸钾氧化结果紫而使其褪色的催化作用,建立了灵敏的催化光度测定痕量亚硝酸根的新方法,测定范围为０．０２－０．１６μｇ／ｍＬ,用于水样中亚硝酸根的测定,获得了满意结果。     

高碘酸钾氧化中性红测定间苯二酚

在酸性和75℃条件下,微量的间苯二酚对高碘酸钾氧化中性红褪色反应具有显著的抑制作用,据此建立了测定间苯二酚的新的动力学光度法。该方法灵敏、快速、操作简便,此法的线性范围为0．1～3．0μg／mL,检出限为0．082μg／mL,对1．0μg／mL的间苯二酚测定11次的相对标准偏差为2．26％。     

A rapid,colorimetric, procedure for determination of fenitrothion

Abstract

Fenitrothion in formulations and on grains is determined colorimetrically as 4‐nitro‐3‐methylphenoxide, after hydrolysis at room temperature catalysed by alkaline peroxide. Interferences in determination of residue levels are removed by filtration of commodity extract through basic alumina or by barium chloride plus excess oxidant.     

A rapid method for determination of Aroclor 1260 in cattle adipose tissue

Abstract

A simple analytical procedure for the determination of Aroclor 1260 in cattle adipose tissue is described. The polychlorinated biphenyls residues are extracted from the tissue using a soxhlet extractor and the extracts are cleaned up using a florisil SEP‐PAK cartridge. The residues are detected using a gas chromatograph equipped with an electron capture detector. The effect of extraction time of the Aroclor 1260 residues from the tissue has been investigated and a period of four hours is found to give satisfactory percent recoveries. Greater than 85 percent recoveries were obtained from adipose tissue spiked with Aroclor 1260. The method can be used to detect Aroclor 1260 residue levels as low as 0.10 parts per million.

The method was used to analyze thirty‐one cattle adipose tissue samples out of which twenty‐six samples were taken from cattle suspected of exposure to a pasture containing electrical transformers and capacitors containing Aroclor 1260. Five control samples were collected from cattle with no known exposure. All twenty‐six samples were found to contain non‐detectable Aroclor 1260 residues.     

环境水中污染物亚硝酸根的现场快速测定研究

通过研制一种环境保护试纸从而能简便快速地现场半定量测定环境水中污染物亚硝酸根,便于野外水环境普查,应用它可使测定时间由标准法的3h左右短到5min,使分析成本大为降低。     

水中余氯现场快速测定方法研究

通过研制一种测试管，从而能简便，快速地测定水中的余氯。该测试管尤其适宜于现场监测。具有快速、简便、抗干扰能力强和价格低廉等特点。     

Investigation of new indirect spectrophotometric method for the determination of carbofuran in carbamate pesticides

A new spectrophotometric method has been investigated for the determination of Carbofuran pesticide. The method was based on the hydrolysis of the pesticides. The hydrolyzed products, methylamine on reaction with sodium nitroprusside solution in acetone medium gives a purple colored solution. The absorbance of the resulting solution was measured at 530 nm. Conditions for the complete hydrolysis of pesticides and quantitative determination of methylamine were optimized. From the standard calibration plot of methylamine, the amount of pesticides was calculated. The amount of active ingredients in commercial products was determined from the amount of methylamine found. It was observed that lower concentration of the active ingredients were present in the commercial products. The limit of detection and quantification was calculated and found to be 0.804 and 2.68 ppm respectively.     

水中钙离子现场快速测定方法研究

通过研制一种测试管 ,从而能简便、快速的测定水中的钙离子。该测试管尤其适宜于现场即时监测 ,具有快速、简便、抗干扰能力强和价格低廉等特点     

Ultraviolet spectrophotometric determination of nitrate: detecting nitrification rates and inhibition.

Simple methods that rapidly detect nitrification inhibition are needed to enforce pretreatment programs and prevent upsets. The objective of this study was to demonstrate a rapid method for measuring nitrification inhibition by using nitrate generation rates (NGRs) coupled with direct UV detection of nitrate. The NGRs were measured with UV spectrophotometry at wavelengths between 225 and 240 nm, without chemical manipulation, and verified against ion chromatography. The method was shown to quickly and accurately measure nitrate concentrations after correcting for nitrite interference. Cadmium, hypochlorite and 1-chloro-2,4-dintrobenzene (CDNB) were tested for their ability to cause nitrification inhibition using this method. The CDNB was found to cause a correctable interference with the test, while hypochlorite provided an uncorrectable interference. Used as a batch method coupled with biotic and abiotic controls, this approach can be deployed at full-scale treatment plants as a relatively rapid (1.5 hours) means of identifying nitrification-inhibiting wastewaters.     

Impact of injection system design on ISCO performance with permanganate--mathematical modeling results

In situ chemical oxidation (ISCO) using permanganate (MnO(4)(-)) can be a very effective technique for remediation of soil and groundwater contaminated with chlorinated solvents. However, many ISCO projects are less effective than desired because of poor delivery of the chemical reagents to the treatment zone. In this work, the numerical model RT3D was modified and applied to evaluate the effect of aquifer characteristics and injection system design on contact and treatment efficiency. MnO(4)(-) consumption was simulated assuming the natural oxidant demand (NOD) is composed of a fraction that reacts instantaneously and a fraction that slowly reacts following a 2nd order relationship where NOD consumption rate increases with increasing MnO(4)(-) concentration. MnO(4)(-) consumption by the contaminant was simulated as an instantaneous reaction. Simulation results indicate that the mass of permanganate and volume of water injected has the greatest impact on aquifer contact efficiency and contaminant treatment efficiency. Several small injection events are not expected to increase contact efficiency compared to a single large injection event, and can increase the amount of un-reacted MnO(4)(-) released down-gradient. High groundwater flow velocities can increase the fraction of aquifer contacted. Initial contaminant concentration and contaminant retardation factor have only a minor impact on volume contact efficiency. Aquifer heterogeneity can have both positive and negative impacts on remediation system performance, depending on the injection system design.     

过硫酸盐在土壤中的电动输运特性

为提高过硫酸盐氧化剂在土壤中的传输效率,对以电渗流为主导因素的电动输运特性进行研究。通过土壤箱体的实验和数值模拟,研究电势梯度、土壤间隙水盐浓度和温度、过硫酸钠投放电极和浓度、pH对电渗流速和电渗系数影响,并分析过硫酸盐电动输运特性。结果表明,过硫酸盐在阳极投放与在两极投放时电动输运效果较好;提高投放的过硫酸盐浓度可以同比例提高相同时刻土壤中的过硫酸根浓度,但不改变电动输运所需的时间;提高电势梯度可以等比例提高电渗流速,但不能提高电渗系数;提高盐浓度可使电渗流速和电渗系数以相同比例提高;土壤升温至60 ℃和在2~12区间内的pH改变对电渗流速和电渗系数的提高比例为14.5%和4.8%;当盐浓度低于0.1 mol·L⁻¹时,在1、2 V·cm⁻¹的电势梯度下,土壤的最大温升分别为8 ℃、40 ℃。因此,在过硫酸盐的电动输运过程中,建议采用1V·cm⁻¹电势梯度以降低过硫酸盐的活化速率。本研究结果可为电动输运过硫酸盐的传输方案提供参考。     

水中氰化物突发性污染事故应急监测方法研究

旨在研究现场快速测定水中的氰化物。运用比色分析的朗伯 比尔定律和真空工艺设计 ,将复杂繁琐的实验室测试方法和操作程序有机地融合在测试管中。该测试管具有快速、简便和价格低廉等特点 ,测定范围为 0 0 0 5— 0 2 0mg/L。     

热活化过硫酸钾降解呋虫胺

以新烟碱类杀虫剂呋虫胺为目标污染物,以过硫酸钾为氧化剂,研究不同热活化条件下过硫酸钾对呋虫胺降解率的影响。实验结果表明:呋虫胺的降解率与溶液中过硫酸钾的浓度成正比;随着温度的升高,呋虫胺的降解率也逐渐升高;虽然中性时呋虫胺的降解率稍高于酸性和碱性时的降解率,但pH的变化对呋虫胺的降解率影响不大;Cl-和HCO3-对反应的影响比较复杂,当溶液中的Cl-和HCO3-的浓度低于5 mmol/L时,均促进呋虫胺的降解,而浓度升高时则抑制呋虫胺的降解;通过添加自由基捕获剂发现,该反应体系中同时存在·SO4-和·OH,但起主要作用的是·SO4-。     

热活化过硫酸盐对双酚A的降解及其机理

研究了热活化过硫酸盐对双酚A的氧化降解效能及机理,探讨了温度,反应物初始浓度,pH值,阴离子和腐殖酸对双酚A降解的影响。结果表明:在实验范围内,双酚A的降解率随温度和过硫酸钠初始浓度的升高而增加;双酚A在酸性条件下的降解率比在中性和碱性条件下要高;阴离子的存在会抑制溶液中双酚A的降解,抑制作用依次为SO42- >Cl- >NO3-;加入腐殖酸后,双酚A的降解受到抑制。双酚A的降解中间产物主要为对苯二酚、对异-丙烯基苯酚、2-甲基-2,3-二氢苯并呋喃和3-甲基-2,3-二氢苯并呋喃。     

Degradation of bisphenol A in aqueous solution by persulfate activated with ferrous ion

Degradation of bisphenol A (BPA) in aqueous solution was studied with high-efficiency sulfate radical (SO₄ ^?·), which was generated by the activation of persulfate (S₂O₈ ^2?) with ferrous ion (Fe²⁺). S₂O₈ ^2? was activated by Fe²⁺ to produce SO₄ ^?·, and iron powder (Fe⁰) was used as a slow-releasing source of dissolved Fe²⁺. The major oxidation products of BPA were determined by liquid chromatography-mass spectrometer. The mineralization efficiency of BPA was monitored by total organic carbon (TOC) analyzer. BPA removal efficiency was improved by the increase of initial S₂O₈ ^2? or Fe²⁺ concentrations and then decreased with excess Fe²⁺ concentration. The adding mode of Fe²⁺ had significant impact on BPA degradation and mineralization. BPA removal rates increased from 49 to 97 % with sequential addition of Fe²⁺, while complete degradation was observed with continuous diffusion of Fe²⁺, and the latter achieved higher TOC removal rate. When Fe⁰ was employed as a slow-releasing source of dissolved Fe²⁺, 100 % of BPA degradation efficiency was achieved, and the highest removal rate of TOC (85 %) was obtained within 2 h. In the Fe⁰–S₂O₈ ^2? system, Fe⁰ as the activator of S₂O₈ ^2? could offer sustainable oxidation for BPA, and higher TOC removal rate was achieved. It was proved that Fe⁰–S₂O₈ ^2? system has perspective for future works.     

Evaluation of flow injection analysis method with spectrophotometric detection for the determination of atrazine in soil extracts

A method for determining atrazine in soil extracts was evaluated by flow injection analysis with spectrophotometric detection. The method is based on the reaction of atrazine with pyridine in an acid medium followed by the reaction with NaOH and sulfanilic acid. Several analytical conditions were previously studied and optimized. Under the best conditions of analysis, the limits of detection and quantification were 0.15 and 0.45 mg L^?1, respectively, for a linear response between 0.50 and 2.50 mg L^?1, and a sampling throughput of 21 determinations per hour. Using the standard addition method, the maximum relative standard deviation of 17% and recovery values between 80 and 100% were observed for three extracts from soil samples with different composition. The proposed method is simple, low-cost and easy to use, and can be employed for studies involving atrazine in soil samples or for screening of atrazine in soils.     

水分快速分析仪测定城市污泥的含水率

污泥含水率是污水处理、污泥处理及污泥处置利用等环节的重要评估指标。本研究采用快速测定法对不同类型城市污泥含水率进行测定,考察了污泥含水率、质量、颗粒度对测定结果影响,并与国标重量法进行比较。结果表明：污泥质量对快速法测定结果影响较小,原始污泥测定结果标准偏差在0.01%~0.05%之间,常规脱水污泥和生物沥浸脱水污泥测定结果标准偏差均为0.03%;相比国标法,脱水污泥含水率越低,快速法测定结果误差越大,常规脱水污泥和生物沥浸脱水污泥测定结果相对误差分别为-2.09%和-3.49%;脱水污泥颗粒度越大,快速法测定结果偏差越大,常规脱水污泥和生物沥浸脱水污泥总体样本标准偏差分别为0.43%和1.25%。另外发现,在相同干化条件下,生物沥浸脱水污泥相对于常规脱水污泥有较快的水分蒸发速度。针对城市污泥,为缩短测定时间和提高工作效率,待测污泥优选质量≤4 g和颗粒度≤3 mm,且建议只在生产运行中使用,室内科研实验优选国标法。     

A rapid and efficient determination of natural estrogens in soils by pressurised liquid extraction and gas chromatography-mass spectrometry

We present a new analytical procedure for the extraction and determination of natural estrogens in soils based on pressurised liquid extraction and GC-MS determination. After testing twelve solvents, acetone proved to be the most efficient extractant. The optimum extraction temperature is 60 degrees C. Soil extracts have to be purified and concentrated by C-18 solid phase extraction. The dried extracts are derivatised by N-methyl-N-(trimethylsilyl)trifluoro-acetamide before measurement by GC-MS. Recoveries of 79-103% with relative standard deviations 相似文献