南京市夏季青菜中有机磷农药残留量调查

１９９４年夏季调查和测定了南京市市售青菜中甲胺磷、乐果、甲基－１６０５等５种有机磷农药残留量。结果表明，夏季青菜（包括青菜秧）中有机磷农药残留量有超标现象，其中甲胺磷在青菜中的平均残留量为０．０６３ｍｇ／ｋｇ，超标率为１１．５％，其余４种有机磷农药在青菜中未检出。     

南京市夏季青菜中有机磷农药残留量调查

１９９４年夏季调查和测定了南京市市售青菜中甲胺磷、乐果、甲基－１６０５等５种有机磷农药残留量。结果表明，夏季青菜（包括青菜秧）中有机磷农药残留量有超标现象，其中甲胺磷在青菜中的平均残留量为０．０６３ｍｇ／ｋｇ，超标率为１１．５％，其余４种有机磷农药在青菜中未检出。     

夏季蔬菜中有机磷农药残留调查

报道了夏季蔬菜中有机磷农药残留量的调查。结果表明：在西红柿、青椒和豆角中，乐果平均残留量为０．０８１ｍｇ／ｋｇ，甲基对硫磷为０．０１５ｍｇ／ｋｇ，二嗪农为０．００３ｍｇ／ｋｇ，而敌敌畏在这三种蔬菜中均未检出。夏季蔬菜中农药残留量的超标率甲基对硫磷＞乐果＞二嗪农＞敌敌畏。三种蔬菜中，豆角的有机磷农药检出率最高，其次为青椒、西红柿。     

有机磷农药废水湿式空气氧化预处理的研究

以ｏ，ｏ－二甲氧基硫代磷酰氯生产废水为代表，在２Ｌ不锈钢高压釜中研究了有机磷农药废水湿式空气氧化预处理工艺，得到了实现有机磷、有机硫去除８０－９０％，ＣＯＤ去除６０％的工艺条件及其优化组合，工艺条件相当缓和，废水处理后，其可生化降解性显著提高，ＢＯＤ５／ＣＯＤ由０．２增至０．４－０．５。工艺条件用于处理其它几中有机磷废水取得同样好的效果。     

测定水中农药残留的新方法

应用已研制出的酶片和显色基质片快速测定水中有机磷和氨基甲酸酯农药. 这种方法能够在田间没有仪器的情况下检测农药的危险水平.对于大多数有机磷氨基甲酸酯农药,其检测灵敏度在見0.1—3.0ppm范围.方法具有快速、经济,容易在田间现场使用的特点。     

蔬菜中有机磷农药残留的发光菌快速检测

本文建立了一种用发光细菌快速检测蔬菜中有机磷农药残留的方法，以３％ＮａＣｌ（Ｗ／Ｖ）溶液从蔬菜中洗涤出残留的农药，加入定量发光菌溶液，通过其发光量的变化来检测农药的含量。分析了发光菌对蔬菜中六种有机磷农药的响应情况，探讨了检测空心菜中甲胺磷农药残留的最佳参数，实验表明，新建立的方法是检测蔬菜中有机磷农药残留的一种快速有效，价廉的方法。     

农药废水中的有机硫,磷污染物湿式空气氧化反应的研究

以ｏ，ｏ－二甲氧基或ｏ，ｏ－二乙氧基硫代磷酰氯废水为典型废水，在１８０－２３０℃，氧气压力为０．７－１．５ＭＰａ的反应条件下，在２Ｌ的不锈钢的高压釜中，研究了农药废中有机硫磷化合物在温式空气氧化过程中的降解机制。实验结果表明，有机硫磷化合物分子中的有机硫通过氧化反应降解为硫，有机磷通过水解反应降解为磷酸。有机硫氧化生成的硫酸是废水湿式空气氧化程中酸度增加的主要来源。酸性条件比碱性条件更利于有机硫磷     

毛细管气相色谱法测定七种热不稳定有机磷农药

本文对热不稳定有机磷农药水胺硫磷、久效磷、磷胺、甲胺磷、亚胺硫磷、乙酰甲胺磷和敌百虫的毛细管气相色谱分析条件进行了考察。当以高流速的氢气（〉２００ｃｍ．ｓ＾－１）为载气时，可明显减少这些有机磷农药的热分解，即使在较高的进样口温度（２８０℃）下，仍可以测定它们的原形。     

蔬菜和水果中残留硫双威的气相色谱分析

本文提出了一种快速、高效提取净化蔬菜、水果中残留硫双威的前处理方法和用火焰光度检测的气相色谱法。该法的最低检出浓度为０．０４ｍｇ·ｋｇ＾－１，在蔬菜，水果中的平均加标回收率分别为９３．０－１０６．７％和９４．５－１０４．２％，变异系数分别为２．５７－６．０５％和２．７４－５．８３％。     

氨的干沉降速度测定

通过对南昌郊区一片樟树林上空氨浓度的实地监测，用微气象学浓度梯度法计算了氨的干沉降速度，在稳定和中性大气情况下，氨的干沉降速度范围为－０．９６－２．０９ｃｍ．ｓ＾－１，平均值为０．６２ｃｍ．ｓ＾－１。     

蔬菜水果中的新烟碱类农药残留量与人群摄食暴露健康风险评价

新烟碱类农药是目前被广泛用于农业中的一类作用独特、高效广谱的内吸性杀虫剂,它们在蔬菜水果中的残留对人体健康构成威胁。本研究目的是查明北京市场上蔬菜水果中不同新烟碱类农药的残留量,并对人群摄食暴露健康风险进行评估。从北京市场上采集49种蔬菜和24种水果,采用Qu ECh ERS–高效液相色谱串联质谱(HPLC-MS/MS)法测定蔬菜水果中9种新烟碱类农药的含量。利用测得数据和中国居民膳食结构调查资料,采用蒙特卡罗模拟方法计算了不同年龄段人群的日均经口摄入暴露量的概率分布,并采用商值法计算了新烟碱类农药的非致癌风险。结果显示新烟碱类农药普遍存在于北京市场上的蔬菜水果中。49种蔬菜样品中检出7种新烟碱类农药,其中吡虫啉、啶虫脒和噻虫嗪检出率均达100%,噻虫胺、烯啶虫胺、噻虫啉和呋虫胺的检出率分别为47%、14%、10%和4%。24种水果样品中检出5种新烟碱类农药,其中吡虫啉和啶虫脒的检出率均达100%,噻虫嗪、噻虫胺和噻虫啉的检出率分别为54%、13%和4%。不同新烟碱类农药在蔬菜水果中的含量范围为0.01 ng·g~(-1)~126 ng·g~(-1),均未超过我国食品安全国家标准或美国联邦管理条例中的限量值。小部分(约3%)人群因摄食蔬菜水果暴露于新烟碱类农药的非致癌风险商值大于0.1。新烟碱类农药在蔬菜水果中普遍存在,对人体健康有潜在的风险。     

High performance liquid chromatographic determination of pesticides in soluble phase and suspended phase in river water

A high performance liquid chromatographic method has been developed to determine pesticides in river water as both dissolved phase and suspended phase. The target pesticides were eight herbicides, asulam, diuron, flazasulfuron, linuron, MCPB, mecoprop, pyrazosulfuron‐ethyl and siduron, and two fungicides, oxine‐copper and thiram. The pesticides in filtered river water were extracted with styrene‐divinylbenzene copolymer and were eluted with acetonitrile. The pesticides on suspended solids were extracted ultrasonically with acetonitrile. Each eluate was concentrated and analyzed by HPLC with multiwavelength detector. Recoveries of the pesticides in the overall procedure of this method were 78–114% for filtered river water and 75–107% for suspended solids. The limits of detection in water and suspended solids ranged from 0.1 to 0.9 μg/L and 1 to 7 μg/g, respectively. Pesticide distribution between soluble phase and suspended phase in river water was measured by this method.     

长春市主要蔬菜中农药残留分析

采用速测法和气相色谱法研究了长春市市场销售的主要蔬菜中的农药残留问题。2002年秋季对长春市的9个蔬菜批发市场的16种蔬菜进行抽样检测，蔬菜中有机磷类和氨基甲酸酯类农药平均超标率为11．05％，残留的主要农药种类是甲胺磷、氧化乐果和敌敌畏。检测16种蔬菜中有9种超标。2003年春季同样对9个蔬菜市场的17种蔬菜进行抽样检测，农药残留平均超标率为11．0％，残留的农药主要种类是甲基对硫磷、对硫磷、甲拌磷、敌敌畏、氯氰菊酯和氰戊菊酯等，检测的17种蔬菜中有3种严重超标。由此可见蔬菜中农药残留还是很严重的问题，政府与有关部门仍需加强管理。     

荧光传感器阵列检测农药污染物研究进展

农药的滥用已造成严重的环境污染,因此开发高效、简便和灵敏的农药检测技术是环境科学领域的研究焦点.荧光传感检测因其灵敏度高,检出限低,操作简单,成本低,目前已逐渐成为农药快速定量检测的一个发展方向.然而,在真实样品检测环境中,污染物不是单独存在的,常伴随结构或化学性质上与待检测分析物相似的污染物进行干扰.而基于阵列的荧光...     

农药对土壤微生物群落的副作用的研究方法(Methods for Detecting Side-Effect of Pesticides to Soil Microbial Communities)

微生物群落在保持土壤肥力和对外界适应能力方面起着十分重要的作用.随着农药的广泛应用和农药评估体系的建立与完善,人们越来越关注农药对土壤微生物群落的负面影响,并且尝试用多种方法进行研究.虽然对其中任何一种方法的使用,均有助于提高人们对农药副作用的认识,但是使用少数几种方法所获得的信息,已能够满足风险评估的最低要求.论文以农药风险评估的"资料要求"为依据,对"资料要求"中涉及的"碳转化"和"氮转化"两种室内试验的特点和设计思路进行了分析.此外还简要介绍了国内外农药管理部门在土壤微生物风险评估中常用的几种模型,并探讨了这些模型与具体试验方法之间的关联.从文中可以看出,对于农药的土壤微生物影响,现已建立起了比较规范化的室内测定方法,目前缺乏的是与风险评估模型相配套的田间试验方法或准则.     

V-shaped substrate for surface and volume enhanced Raman spectroscopic analysis of microplastics

● V-shaped substrate was obtained for SERS analysis of microplastics (diameter ≈ 1 μm). ● Enhancement factor of V-shaped substrate can reach 20 in microplastics detection. ● V-shaped nanopore array can bring additional volume enhancement. ● V-shaped substrate was more economic in application compared to Klarite substrate. Research on the microplastics (MPs) is developing towards smaller size, but corresponding methods for the rapid and accurate detection of microplastics, especially nanoplastics still present challenge. In this work, a novel surface and volume enhanced Raman spectroscopy substrate was developed for the rapid detection of microplastic particles below 5 μm. The gold nanoparticles (NPs) were deposited onto the surface and into the V-shaped nanopores of anodized aluminum oxide (AAO) through magnetron sputtering or ion sputtering, and then AuNPs@V-shaped AAO SERS substrate was obtained and studied for microplastic detection. SERS performance of AuNPs@V-shaped AAO SERS substrate was evaluated through the detection of polystyrene and polymethyl methacrylate microspheres. Results indicated that individual polystyrene sphere with a diameter of 1 μm can be well detected on AuNPs@V-shaped AAO SERS substrate, and the maximum enhancement factor (EF) can reach 20. In addition, microplastics in ambient atmospheric samples were collected and tested to verify the effectiveness of the AuNPs@V-shaped AAO SERS substrate in the real environment. This study provides a rapid, economic and simple method for detecting and identifying microplastics with small size.     

新烟碱类农药在我国的登记现状及对蜜蜂的初级风险评估

调研已开发的包括吡虫啉、噻虫嗪、噻虫胺、啶虫脒、噻虫啉、呋虫胺、烯啶虫胺、环氧虫啶、氯噻啉、哌虫啶和氟啶虫胺腈在内的11种新烟碱类农药在我国的登记现状。根据已登记的新烟碱农药的使用方法,开展了不同暴露场景下蜜蜂的初级风险评估。结果表明,喷施场景下,吡虫啉、噻虫嗪、噻虫胺、烯啶虫胺、呋虫胺、氟啶虫胺腈和氯噻啉这7种新烟碱类农药在不同作物上使用对蜜蜂的风险商值均大于1,风险均不可接受;啶虫脒、哌虫啶和噻虫啉在所有登记作物上使用对蜜蜂的风险商值均小于1,风险可接受。土壤或种子处理场景下,除噻虫啉外,其余4种新烟碱类农药包括吡虫啉、噻虫胺、噻虫嗪和呋虫胺对蜜蜂的风险商值均大于1,风险均不可接受。评估结果可为新烟碱类农药在我国的登记管理提供科学参考。     

Quantification of pesticide residues on plastic mulching films in typical farmlands of the North China

• Pesticide residuals on mulching film of Shandong, Tianjin and Hebei. • Detected 29 pesticides in soil and 30 in mulching film. • Pesticides on plastic films: 86.4‒22213.2 ng/g and in soil: 9.3‒535.3 ng/g. • Pesticides on plastic films 20 times higher than in soil. Plastic debris as new pollutants attracts much attention in the recent years. The plastic mulching films is one of the most important plastic debirs source in the environment. The aim of this work was to investigate the current status of pesticide residues on the plastic mulching films. Based on the QuEChERS method, multi-residue methods for detection of pesticide residues with gas chromatography tandem mass spectrum (GC-MS) and high performance liquid chromatography tandem mass spectrum (HPLC-MS) were developed for the analysis of the pesticides residues in plastic film and soil samples from Tianjin, Hebei and Shandong. The total concentrations of pesticide residues were in the range of 86.4‒22213.2 ng/g in plastic film debris, which was about 20 times higher than that in soil (9.3‒535.3 ng/g). Residual level of pesticides varied greatly in different samples. The historical usage and recent application of pesticides were the main sources for pesticide residues on plastic films and soil. In short, plastic mulching films could act as a sink for pesticides in farmland and the ubiquitous pesticide residues on plastic films should draw more attention.     

Estimating the uncertainty of pesticide residue analysis from mango using multi-residue analysis and validation of method

Validation of method was performed for various pesticides on mango matrix involving the processing of sample at ambient and cryogenic conditions. The linearity, limits of detection, repeatability, matrix effect, and recovery were studied as the aspects of method validation. The effect of matrix on recovery was found to be medium (20–50%) and strong (>50%). After correction by matrix-matched calibration curves, the recovery was calculated to be in the range of 80–107% and 80–105% at ambient and cryogenic processing, respectively. The precision estimated for the recovery of pesticides obtained from both solvent- and matrix-matched calibration curves and at both the processing conditions was determined to be >20% except for chlorpyrifos and atrazine. The uncertainty established for the methodology was >20%, which substantiates the efficiency and reliability of methodology used for pesticide residue analysis in mango in this study.