空气中农药六六六的气相色谱法测定

空气中农药样品的采集和分析,已经发展了很多方法和技术设备。概括起来说,用滤膜及利用重力惯性等方法采收漂尘,吸附的方法收集蒸汽、液体吸收方法来采取漂尘和农药蒸汽样品。分析手段主要是用气相色谱,需要时可与柱色谱,薄层色谱等结合起来以分析复杂的样品。我们采用二甲基甲铣铵作为吸收剂,吸收空气(包括漂尘和蒸汽)中的农药六六六,用气相色谱法进行测定。从吸收剂中萃取农药的方法及色谱分析条件,参照水样中农药六六六,DDT的     

三维荧光联合气相色谱/质谱快速溢油鉴别技术研究

通过一个具体溢油事例的研究,提出了通过三维荧光联合气相色谱/质谱(GC/MS)进行海面溢油鉴别的方法。采用三维荧光指纹信息(谱图形状、荧光特征峰位置、荧光特征峰强度)对14个可疑溢油源样品进行筛选,排除了13个可疑溢油源样品后,再利用GC/MS方法对溢油样品以及剩余可疑溢油源样品中难降解的生物标志化合物(饱和链烷烃、萜烷、甾烷、多环芳烃)进行分析,计算相应的诊断比值并采用"重复性限"方法进行溢油样品和可疑溢油源样品的鉴别分析。结果表明,溢油样品与其中的一个可疑溢油源样品一致,为同一来源;采用三维荧光联合GC/MS进行海面溢油鉴别,既可保证鉴别的准确性,又可大幅度减少检测工作量,缩短鉴定周期。     

砷形态分析中的样品前处理方法

本文对近10多年来砷形态分析中样品的前处理技术及其在不同样品中的应用进行了总结和评述，指出，断续低功率微波辅助提取，经典索氏取和纯乙醇冷冻离心提纯这3种砷化物前处理技术较其他方法更具优势。     

水中放射性核素铯-137测量的不确定度评估

放射性核素利用化学载带、浓缩后进行测量,化学前处理步骤比较复杂,通过分析测量实验中的不确定度和分析计算公式中的有关参数,了解到分析水中放射性核素铯-137时,主要受到样品测量、仪器探测效率、样品化学回收率和样品取样体积等方面的不确定度因素的影响。     

地质样品中Te的分析方法研究

Te是发展高科技产业不可缺少的半导体材料之一,被广泛应用于冶金、石油化工、电子电气、玻璃陶瓷和医药等行业.同时,Te又是一种潜在的环境污染元素.Te在地壳中含量低而分散,寻找高灵敏度的地质样品中Te的检测分析方法一直是人们关注的问题.重铬酸钾容量法、碘量法、极谱法、分光光度法等常见测Te方法灵敏度不够理想,操作步骤也较繁琐.评述了1995-2009年地质样品中Te的检测方法概况及其发展趋势,重点对样品的前处理方法、氢化物发生/原子荧光法和电感耦合等离子体质谱法的优缺点进行了阐述和讨论,指出利用高能效的分离技术达到各形态的有效分离和利用选择性强、灵敏度高的元素特征检测器来达到超痕量形态的测定仍将是地质样品中Te分析的研究趋势.     

利用复介电常数和BPAT神经网络进行环境监测的可行性研究

土壤中的污染物成分复杂，其含量与复介电常数之间具有很强的非线性关系。以土壤样品复介电常数的实部、虚部分别作为输入，以其含水率、体密度和所含6种已知离子的浓度分别作为输出，建立BP人工神经网络。把吉泰兰地区的土壤样品数据分为训练样本集和检验样本集，网络训练后，其学习效果显示模型的性能很好，检验样本的预测结果也与实测值较好吻合，说明利用复介电常数和BP人工神经网络进行环境监测是一种好的方法。     

黄酒中尿素的测定

二乙酰－肟分光光度法是测定黄酒等样品中尿素含量的一种快速、灵敏、简便的方法。样品中的尿素与显色试剂在沸水浴中发色１０￣１５ｍｉｎ后比色测定，显色的线性范围在０￣９μｇ尿素之间。测得的结果中包含了瓜氨酸的含量。样品中酒精和葡萄糖的存在不干扰测定。以标准加入法进行定量，从而使该方法的回收率和重现性大大提高，可满足一般痕量分析的要求。     

田湾核电站外围辐射环境监测工作的质量保证

总结了田湾核电站外围辐射环境监测中的质量保证实施情况，包括：人员培训和考核，仪器设备溯源，样品采集、运输、贮存及生物样品前处理的质控，样品分析和现场监测的质控，数据的记录处理和管理要求等，最后提出几点建议。     

荧光素酶报告基因法测定飞灰中二噁英类物质

荧光素酶报告基因法(CALUX)相比高分辨气相色谱/质谱法(HRGC/HRMS)测定二噁英浓度时,具有分析周期短、检测成本低、灵敏度高(皮克水平)、能反映样品的毒性总量且可进行高通量检测等优点。实际应用时,可先用CALUX对样品作初步筛选检测,再将筛选出的阳性样品用化学分析法作进一步定性定量检测。通过对42个垃圾焚烧飞灰样品同时进行HRGC/HRMS和CALUX分析,得到两者的换算系数,从而可以利用快速检测的结果和换算系数来推算HRGC/HRMS的结果。实验表明,CALUX结果与HRGC/HRMS结果具有很好的线性相关性(R=0.96),换算系数为0.332。该换算系数与日本得到的结果不同,表明中国飞灰性质有别于日本飞灰。而且,不同环境介质之间换算系数也不一致。为增加该方法在中国的适用性,必须通过实验方法找出符合中国样品的换算系数。     

质量控制在水质分析中的应用

质量控制是实验室化学分析的一种有效的科学管理方法,它包括外部质量控制和内部质量控制。外部质量控制一般每年作一次或两次参考样品的分析,以了解或证实该实验室提供可信数据的能力;内部质量控制系指分析未知样品时作控制样品的分析,以鉴别未知样品的分析结果的可靠性。本文结合实际工作,重点介绍实验室内部质量控制的方法。现将水质分析中质量控制的方法、影响质量控制的基本因素等分述如下。     

Chloroaromatic pollutants in mussels incubated in two finnish watercourses polluted by industry

Concentrations of different chlorinated compounds were measured in mussels incubated in two polluted watercourses, a river (the River Kymijoki) and a lake (Lake Vanaja) for four weeks in summer 1995. The sum concentrations of polychlorinated phenols (PCP) and biphenyls (PCB) were both about 1 μg/g lipid weight (lw) in Lake Vanaja mussels, while in the River Kymijoki mussels PCPs were non-detectable and PCBs were measured 120 ng/g lIw. The concentrations of toxic polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners ranged between <17 and 370 pg/g Iw in Lake Vanaja mussels and between <38 and 11,000 pg/g lw in the River Kymijoki mussels. Polychlorinated diphenyl ethers (PCDE) were detected in the mussels incubated in the River Kymijoki (0.4–1.1 ng/g Iw), but not in those incubated in Lake Vanaja. Polychlorinated phenoxyanisoles (PCPA) were measured 33 ng/g lw and polychlorinated phenoxyphenols (PCPP) 300 ng/g lw in the mussels incubated in the River Kymijoki. PCPAs were also detected in reference samples, which were sediment and pike from the River Kymijoki and Baltic salmon, seal and white-tailed sea eagle.     

Book review

The Pesticide Manual ‐ A World Compendium, 8th Edition, C.R. Worthing, Editor and S.B. Walker, Assistant Editor, British Crop Protection Council, BCPC Publications Sales, Bear Farm, Binfield, Bracknell, Berkshire RG12 5QE, England. 1987, 1100 pp., UK £50; Overseas £56. ISBN 0–948404–01–9.     

Organochlorine compounds in a three-step terrestrial food chain

The concentrations of 15 organochlorine chemicals (PCBs and pesticides) were studied in a Central European oak wood food chain system: Great tit (Parus major), caterpillars (Tortrix viridana, Operophtera brumata, Erannis defoliaria), and oak-leaves (Quercus robur). Juvenile tits receive organochlorines from the mother via egg transfer and, eventually to a greater extent, from the caterpillar food source during nestling period. The concentrations of PCB 153 (2,2′,4,4′,5,5′-hexachlorobiphenyl, the most abundant in this study) was found in leaf material at ca. 1 ng/g, in caterpillars 10 ng/g, and in bird eggs 170 ng/g on an average and on a dry mass basis.     

The chemical stability of formulations of some hydrolyzable insecticides in aqueous mixtures with hydrolysis catalysts

Abstract

The active ingredients in commercial formulations of malathion, oxamyl, carbaryl, diazinon, and chlorpyrifos diluted to “spray tank”; concentrations with buffered distilled or natural water of pH 4–9 were stable for at least 24 hr. Formulations of trichlorfon were not stable at pH 7 or above but disappearance rates were slower than for the pure chemical in homogeneous solution. Cupric ion was observed to be an effective catalyst for the hydrolysis of a variety of pure organophosphorus insecticides but did not catalyze hydrolysis of the active ingredients of the formulations examined. Increasing the dilution of the formulation increased the susceptibility of malathion, oxamyl, and carbaryl to hydrolysis.     

Radionuclides in pinon pine (Pinus edulis) nuts from los alamos national laboratory lands and the dose from consumption

Abstract

One of the dominant tree species growing within and around the eastern portion of Los Alamos National Laboratory (LANL), Los Alamos, NM, lands is the pinon pine (Pinus edulis). Pinon pine is used for firewood, fence posts, and building materials and is a source of nuts for food—the seeds are consumed by a wide variety of animals and are also gathered by people in the area and eaten raw or roasted. This study investigated the (1) concentration of ³H, ¹³⁷Cs, ⁹⁰Sr, ^totU, ²³⁸Pu, ^{239, 240}Pu, and²⁴¹ Am in soils (0‐ to 12‐in. [31 cm] depth underneath the tree), pinon pine shoots (PPS), and pinon pine nuts (PPN) collected from LANL lands and regional background (BG) locations, (2) committed effective dose equivalent (CEDE) from the ingestion of nuts, and (3) soil to PPS to PPN concentration ratios (CRs). Most radionuclides, with the exception of ³H in soils, were not significantly higher (p < 0.10) in soils, PPS, and PPN collected from LANL as compared to BG locations, and concentrations of most radionuclides in PPN from LANL have decreased over time. The maximum net CEDE (the CEDE plus two sigma minus BG) at the most conservative ingestion rate (10 lb [4.5 kg]) was 0.0018 mrem (0.018 μSv); this is far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem (1000 μSv). Soil‐to‐nut CRs for most radionuclides were within the range of default values in the literature for common fruits and vegetables.     

Degradation and sorption of imidacloprid in dissimilar surface and subsurface soils

Degradation and sorption/desorption are important processes affecting the leaching of pesticides through soil. This research characterized the degradation and sorption of imidacloprid (1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidinimine) in Drummer (silty clay loam) and Exeter (sandy loam) surface soils and their corresponding subsurface soils using sequential extraction methods over 400 days. By the end of the incubation, approximately 55% of imidacloprid applied at a rate of 1.0 mg kg^?1 degraded in the Exeter sandy loam surface and subsurface soils, compared to 40% of applied imidacloprid within 300 days in Drummer surface and subsurface soils. At the 0.1 mg kg^?1 application rate, dissipation was slower for all four soils. Water-extractable imidacloprid in Exeter surface soil decreased from 98% of applied at day 1 to > 70% of the imidacloprid remaining after 400 d, as compared to 55% in the Drummer surface soil at day 1 and 12% at day 400. These data suggest that imidacloprid was bioavailable to degrading soil microorganisms and sorption/desorption was not the limiting factor for biodegradation. In subsurface soils > 40% of ¹⁴C-benzoic acid was mineralized over 21 days, demonstrating an active microbial community. In contrast, cumulative ¹⁴CO₂ was less than 1.5% of applied ¹⁴C-imidacloprid in all soils over 400 d. Qualitative differences in the microbial communities appear to limit the degradation of imidacloprid in the subsurface soils.     

Biochemical interaction of six op delayed neurotoxicants with several neurotargets

Abstract

Five organophosphorous insecticides: Leptophos, EPN, Cyano‐fenphos, trichloronate and salithion proved to cause irreversible ataxia not only to chicken but also to mice and sheep. TOCP was included as a reference. Cyanofenphos blocked the catecholamine B‐receptor binding activity with ³H‐norepinephrine at a level similar to that of the specific inhibitor propranolol in the mouse heart preparation. In the lamb heart preparation, the B‐receptor was more sensitive to Leptophos, salithion and TOCP than to propranolol. The six compounds and their oxons were screened for their in‐vitro inhibition to monamine oxidase (MAO), acetyl cholinesterase (AChE) and neurotoxic esterase (NTE) in the brain of either mouse, lamb or chicken. It is believed that their AChE inhibition stands for their acute toxicity, while NTE inhibition is responsible for their paralytic ataxia.     

土壤中砷的化学平衡

本文比较详细地综述了砷的化学特性,环境背景值及来源和循环,土壤中砷的三大化学平衡即沉淀溶解平衡,氧化还原平衡,吸附解吸平衡,以及微生物对砷的转化。     

Elemental uptake by edible herbs and lettuce (Latuca sativa)

The total concentration of toxic elements (aluminum, cadmium, chromium and lead) and selected macro and micro elements (iron, manganese, copper and zinc) are reported in six leafy edible vegetation species, namely lettuce, spinach, cabbage, chards and green and red types of Amaranth herbs. Although spinach and chards had greater than 125 mv of iron, both the amaranthus herbs recorded > than 320 μ g g^{? 1} dry weight. In both the spinach and chard species, the Mn and Zn levels were appreciable recording > 225 μ g g^{? 1} and 150 μ g g^{? 1} dry weight, respectively. Aluminum concentrations were (in μ g g^{? 1} dry weight) lettuce (10), cabbage (11), spinach (167), chards (65), amaranthus green (293) and amaranthus red (233). All the micro and macro elements and the toxic elements (Ni, Cr, Cd and Pb) elements analyzed, were below the recommended maximum permitted levels (RMI) in vegetables. Further the elemental uptake and distribution of the nine elements, at three growth stages of the lettuce plant grown on soil bed under controlled conditions are detailed. In the soil, except for iron (16%), greater than 33% of the other cations were in exchangeable form. Generally in the lettuce plant, roots retained much of the iron (> 224 μ g g^{? 1}) and aluminum (> 360 μ g g^{? 1}), while leaves had less than 200 μ g g^{? 1} of iron and 165 μ g g^{? 1} of Al. Although the concentrations of elements marginally decreased with growth, the lettuce leaves had significant amounts of Mn (30 μ g g^{? 1}), Zn (50 μ g g^{? 1}) and Cu (3.6 μ g g^{? 1}). Some presence of lead in leaves (2.0 μ g g^{? 1}) was noticed, but all the toxic and other elements analyzed were well below the RMI values for the vegetables.     

The dissipation of nonlyphenol in stream and pond water under simulated field conditions

Abstract

The dissipation of 1.0 ppm nonylphenol in stream and pond water, incubated in flasks at 16°C under simulated field conditions up to 44 days indicated that the half‐life was 2.5 days if the flasks were open, and 16 days if they were closed. A transformed product was detected in the closed flasks.

Translocation of nonylphenol in water occurred when treated water samples were incubated in the presence of sediment. After 10 days, nonylphenol was detected only in the sediment, but not in water (detection limit = 10 ppb). About 80% of the nonylphenol was degraded in 71 days, but no degradation occurred if the water and the sediment were autoclaved prior to incubation.