电解铝企业阳极残渣、阳极残极浸出毒性鉴别及管理建议

对电解铝企业产生的阳极残渣、阳极残极浸出毒性进行了鉴别。鉴别结果表明：电解铝企业产生阳极残渣浸出液中氟化物（不含氟化钙）平均质量浓度为140 mg／L,最高达244 mg／L,且超标试样数达到《危险废物鉴别标准浸出毒性鉴别》中相应规定,鉴别该废物属于危险废物,应按照危险废物进行管理;阳极残极浸出液中氟化物（不含氟化钙）平均质量浓度为74 mg／L,无超标试样数,该废物不属于具有氟化物浸出毒性的固体废物,建议仍按一般固体废物进行管理。     

微波萃取-气相色谱/质谱法测定土壤中的有机氯农药

通过微波萃取提取土壤中的有机氯农药,萃取溶液经浓硫酸脱色、佛罗里硅土柱净化,最后用气相色谱/质谱法分析.以石英砂为基体进行加标回收测定,有机氯农药的回收率在75.5%～103%之间,检出限为0.01μg/kg.     

铝合金的实验室盐雾试验腐蚀行为图像特征提取

目的提取铝合金材料在盐雾箱试验中可以表征腐蚀程度的表面形貌图像特征量。方法首先,对采集于表面化学清洗过的试样原始图像进行图像增强等预处理,突出腐蚀部位;其次,基于数字图像处理的分形和小波分解方法提取出分形维数和小波能量特征值。结果与以质量损失量为基础的腐蚀深度特征值进行相关性对比,基于图像分析的特征提取法的准确度和精度比较高。结论该方法可以应用于对试样的腐蚀程度进行定性和定量分析,判断并预测试样的腐蚀速度。     

铬渣中铬的浸出行为

采用BCR法连续浸提研究铬渣中铬的存在形态,结果表明:铬渣中总铬和六价铬主要以残渣态和可氧化态形式存在;通过铬渣动态连续浸提实验与静态浸提实验研究了浸提剂和活性炭对铬渣中铬浸出行为的影响,研究发现p H值为3.1的醋酸浸提剂浸出液中铬浓度最低,且添加活性炭后的静态浸出液中铬的浓度有不同程度降低。     

Direct supercritical fluid extraction from water

Abstract

This paper describes the development of apparatus suitable for direct supercritical fluid extraction of organics from water. Results are presented for the extraction of pentachlorophenol present in water at concentrations of the order of 0.1 ppm. The effect of changes in apparatus design and supercritical fluid flow rate on recovery are discussed.     

Microwave extraction of incurred salinomycin from chicken tissues

Abstract

A rapid, accurate, environmentally friendly and cost‐effective microwave extraction technique was developed for the extraction of spiked and incurred salmomycin from chicken tissues (kidney, liver, muscle, ovarian yolk and fat). Extraction of salinomycin from various tissues was achieved by irradiating the sample in absolute ethanol and 2‐propanol (15+2) for 9 sec. in a common household microwave oven. The extract was analysed without further cleanup by HPLC on a C₁₈ column (5 μm) and detected at 592 nm via post‐column reaction with 4‐dimethylaminobenzaldehyde (DMABA) in a heated reactor coil at 86° C. Recoveries of salinomycin from spiked tissues at 30 ng/g level ranged between 87 and 100%. The limit of quantitation was found to be 10 ng/g. The developed method was applied for the analysis of incurred tissues and ovarian yolk of laying chickens given sodium salinomycin in feed at different levels for 14 consecutive days followed by withdrawal periods. Residues were detected in all tissues and ovarian yolk at 0 withdrawal time but declined during the withdrawal period. Highest residue were found in fat and ovarian yolk.     

泄漏检测与维修技术在芳烃抽提装置的应用研究

采用泄漏检测与维修（ LDAR）技术进行了全面检测和统计分析，分析泄漏的原因并通过维修减少泄漏。结果表明：芳烃抽提装置容易泄漏的元件主要为连接件和阀门，主要分布在泵区；SV≥5000μmol／mol的泄漏密封点占总密封点数的0.57％，对总泄漏量的贡献达到了82％，是造成泄漏排放的主要部分。设备管阀件泄漏造成的加工损失率为0.0009％，泄漏点停工维修修复率为83％，停工维修后整体泄漏率为0.03％；VOCs减排率为71％。     

中和-络合萃取-双极膜电渗析处理金刚烷胺制药废水

采用中和沉淀-络合萃取-双极膜电渗析组合工艺协同处理金刚烷胺制药胺化废水与溴化废水.结果表明,通过胺化废水与溴化废水的中和反应,可以大幅消减废水中溶解性固体和有机污染物,避免后续萃取过程中的乳化现象.在pH值为8.0、油/水相比为1∶1的条件下,P204∶正辛醇=3∶2的复配萃取剂对废水中TOC和TN的萃取效率分别为56.9%和20.6%,金刚烷胺及其衍生物几乎被完全萃取.以2.0 mol·L-1的HCl溶液为反萃取剂,可以将47.5%的金刚烷胺从负载有机相中反萃分离,再生后的萃取剂可以多次重复使用.对萃余液采用双极膜电渗析进行处理,可以去除64.2%的无机盐和部分有机物,同时还能回收到较高浓度的酸,但由于氢离子的渗漏难以回收高浓度的碱.     

Analysis of trace dicyandiamide in stream water using solid phase extraction and liquid chromatography UV spectrometry

An improved method for trace level quantification of dicyandiamide in stream water has been developed. This method includes sample pretreatment using solid phase extraction. The extraction procedure (including loading, washing, and eluting) used a flow rate of 1.0 mL/min, and dicyandiamide was eluted with 20 mL of a methanol/acetonitrile mixture (V/V = 2:3), followed by pre-concentration using nitrogen evaporation and analysis with high performance liquid chromatography–ultraviolet spectroscopy (HPLC–UV). Sample extraction was carried out using a Waters Sep-Pak AC-2 Cartridge (with activated carbon). Separation was achieved on a ZIC^®-Hydrophilic Interaction Liquid Chromatography (ZIC-HILIC) (50 mm × 2.1 mm, 3.5 μm) chromatography column and quantification was accomplished based on UV absorbance. A reliable linear relationship was obtained for the calibration curve using standard solutions (R² > 0.999). Recoveries for dicyandiamide ranged from 84.6% to 96.8%, and the relative standard deviations (RSDs, n = 3) were below 6.1% with a detection limit of 5.0 ng/mL for stream water samples.     

SPE-UPLC-MS/MS法测定地下水中多种农药残留

采用固相萃取超高效液相色谱串联质谱法(SPE-UPLC-MS/MS)同时测定地下水中涕灭威、克百威、2,4滴和五氯酚等4种农药残留,通过优化试验条件,使方法在10.0μg/L～200μg/L范围内线性良好,检出限为0.003μg/L～0.006μg/L.标准溶液低、中2个质量浓度水平的加标回收率为84.1％ ～98.8...