Dissipation of Endosulfan and Dichlorvos Residues In/On Cauliflower Curds

Dissipation behaviour of endosulfan and dichlorvos in/on cauliflower, variety Snowball-16, was studied during rabi season (Sep.–March) 2003–2004. Endosulfan and dichlorvos were sprayed @ 350 and 110g a.i. with 115 g a.i., respectively, 80 days after transplanting. Samples were taken at the interval of 0 (1h after spray), 3, 5, 7, and 10 days after spray (DAS) in triplicate and residues were estimated on GC-ECD system equipped with capillary column. The initial deposits of 3.452 and 0.295μgg⁻¹ of endosulfan and dichlorvos dissipated to 0.084 (97.56%) and 0.009 (96.95%), respectively after 10 DAS. Residues of endosulfan reached below maximum residue limit of 2μgg⁻¹ one day after spray and of dichlorvos were below MRL value of 0.5μgg⁻¹ even on 0 day. Dissipation pattern followed first order kinetics for both the insecticides with half life periods of 1.81 and 2.08 days for endosulfan and dichlorvos, respectively.     

液膜分离技术处理含Cr6+废水的研究

采用液膜分离技术处理Cr^6＋质量浓度为200—1000mg／L的废水,考察了膜溶剂、载体、内水相、外水相、pH、乳水比（乳液与废水的体积比）等因素对处理效果的影响,通过正交实验得出最佳实验条件。结果表明,在膜溶剂为煤油、载体为三辛胺、内水相为氯氧化钠、氢氧化钠质量分数为2％、pn为1、乳水比为1：4的最佳条件下,Cr^6＋的去除率可达98．4％。     

水环境中26种类固醇激素的分析方法研究

建立了固相萃取-超高效液相-串联质谱法同时测定水环境中26种类固醇激素的分析方法。明确了取样体积为500 m L,Cleanert PEP为富集柱,乙酸乙酯为洗脱剂,甲醇为溶剂进行提取操作。选择了正离子模式,以0. 1%甲酸/甲醇-水为流动相,负离子模式以0. 1%氨水/乙腈-水为流动相,试样经AcquityTMUPLC BEH C18色谱柱分离后,选用质谱检测模式进行定性、定量分析。通过方法验证,26种类固醇激素的方法检出限为0. 3～1. 5 ng/L,测定下限为1. 2～6. 0 ng/L,代表性样品测定结果的相对标准偏差为2. 6%～13. 7%(n=6),加标回收率为71. 2%～121%。该方法操作便捷,灵敏度高,精密度和准确度良好,可适用于水环境中多种痕量、超痕量类固醇激素的定性定量分析。     

Pressurized liquid extraction of six tetracyclines from agricultural soils

Veterinary antibiotics used in agriculture can be introduced into the environment through land application of animal manure, accumulating in soils and groundwaters and posing a significant risk to human health and animal well-being. As the analysis of tetracyclines in soil is challenging due to their strong interaction with soil minerals and organic carbon, the objective of this study was to develop a reliable and reproducible method for quantitative analysis of chlortetracycline and oxytetracycline, and their respective metabolites in soils. A method based on pressurized liquid extraction (PLE) with in-cell clean-up was developed for the extraction of chlortetracycline and oxytetracycline and four likely metabolites from a set of four soils. Optimized conditions included a cell size of 22?mL, soil loading of 5?g, pH of 8.0, methanol:water ratio of 3:1, 50?°C, and two cycles. Soil extracts were analysed by high-performance liquid chromatography (HPLC) coupled with ion trap mass spectrometry (MS). Recoveries of seven tetracyclines from soil ranged from 41% to 110%. The limits of detection for tetracyclines were 0.08–0.3 µg g^?1 soil, and intra- and inter-day variation ranged from 0.12–0.34%. The proposed PLE method is suitable for quantification of tetracyclines in agricultural soils at typical concentrations expected in contaminated environments.     

P204为载体的微乳液膜处理焦化厂含酚废水的研究

研究了以P204为载体的Span80/煤油/NaOH微乳液膜配方及其稳定性,通过该液膜体系萃取废水中酚的研究,考察了P204与Span80的质量比、乳水比、萃取时间、油相的重复使用次数等对除酚率的影响。实验结果表明,在优化条件下,采用P204/Span80/煤油/NaOH微乳液膜处理焦化厂中高浓度的含酚废水,一次性除酚率均高于99%,且对高浓度含酚废水的除酚效果更佳;微乳液膜不仅稳定性好,传质速率高,除酚效率高,而且可自动破乳,油相可重复使用。     

烹饪油烟污染与处理技术探讨

为了降低油烟对环境的污染,分析了油烟中的主要污染物成分及油烟对人体健康的几种危害。讨论了五种油烟净化技术:惯性分离法、过滤分离法、液体洗涤法、静电沉积法、复合技术。分析了液体洗涤油烟净化技术的原理、水循环利用时对洗涤废液进行的油水分离,提出了采用流场分析喷淋,以了解其流场的特性。结果表明,采用液体洗涤法去除油烟效率高,安全可靠。     

液体旋流分离器分离效率的研究

液体旋流分离器是水环境污染治理的主要设备之一.分离效率是衡量液体旋流分离器分离过程进行完善程度的最重要的技术指标,它能从质与量两方面反映出设备性能的优劣.当前液体旋流分离器设计过程还缺少具体量化的理论依据,为了给液体旋流分离器的设计提供理论依据,通过液体旋流分离器从水中分离固体粒子的性能实验,得出了液体旋流分离器各部结构尺寸、形状、相对比例对分离效率的不同影响程度,提出了结构参数的最佳取值范围.按照本研究提出的设计原则和方法,可以制造出性能优良的液体旋流分离器.     

环境监测实验室废液的管理与处理方法

环境监测实验室的废液处理常常被忽视,提出建立有效的废液管理制度的必要性.有针对性地介绍了环境监测实验室中常见废液的处理方法.     

固相萃取-UPLC-MS/MS法测定环境水体中多种抗生素

采用固相萃取-超高效液相色谱串联质谱法测定环境水样中25种磺胺类和喹诺酮类抗生素,通过优化试验条件,使方法在2.00μg/L～200μg/L范围内线性良好,方法检出限为1.01ng/L～2.85ng/L,7次测定结果的RSD为2.3%～8.0%。将该方法用于自来水和地表水测定,结果均为未检出,高、低质量浓度水平的加标回收率为61.2%～102%。     

HPLC-三重四级杆质谱法测定医疗废水中抗生素残留

采用固相萃取/高效液相色谱-三重四级杆质谱法同时测定医疗废水中的20种超痕量抗生素残留,通过优化试验条件,使方法在100μg/L～100μg/L范围内线性良好,方法检出限为024ng/L～122ng/L。空白水样和实际水样3个质量浓度水平的加标回收率分别为80.2%～108%和75.8%～114%,6次测定结果的RSD分别为2.4%～8.4%和1.7%～8.1%。将该方法用于测定重庆市2家三甲医院医疗废水中的超痕量抗生素残留,结果有11种抗生素检出,其余均为未检出。