废水中硝基苯类化合物测定方法的探讨及新方法研究

探讨了废水中硝基苯类化合物的气相色谱法测定方法中的水样预处理操作繁琐,实验耗时长,且萃取时使用易挥发有毒有害的有机物二氯甲烷。另一种常见的测定方法还原-偶氮分光光度法,而染料、印染制革等工业废水的颜色较深,对测定造成干扰,通常通过蒸馏预处理消除水样颜色带来的干扰,而在蒸馏过程中因硝基苯类沸点较高不能将水样中的硝基苯类化合物全部蒸出,导致检测结果偏低。提出了一种经聚己内酰胺脱色,简单又快捷地消除水样中颜色的干扰,又避免了硝基苯类化合物蒸馏不完全的问题,再利用还原-偶氮分光光度法准确测定废水中硝基苯类化合物的方法。     

湿地植被对污水净化效果分析研究

人工湿地植被种植对污水净化具有显著性的改善作用,分析人工湿地植被种植与污水净化的量化关系,分析人工湿地植被种植对污水改善的原理,建立生态植被污水净化处理模式,采用多元回归分析方法人工湿地植被对水质控制和小型富营养水体生态恢复的效益因素,以营养物的去除率、重金属的去除率以及有机物去除率为指标,分析人工湿地植被种植对污水净化的生态学改善模型。研究表明,人工湿地植被种植能增加水体透明度,降低水体中的富营养物和重金属等物质,对污水具有显著性的改善作用。     

A study on the interactions among several plant secondary compounds and aphids

The research, focused on the specific interactions among seven plant secondary compounds and aphids, was carried out and the preliminary results showed: (1) "T-typed tube method" was regarded as the best method compared with others designed to observe the interactions. (2) Cabbage aphid was able to be attracted by laurolene while it was not susceptible to α-pinene, β-pinene and diamylene. (3) Gossypol, a major secondary substance in cotton, was able to be implicated as feeding attractant to cotton aphid. (4) Rutin might be implicated repellent to cotton aphid.     

青铜峡铝厂氟污染对广武乡玉米影响的调查分析

监测了青铜峡铝厂东南方向４．５ｋｍ的广武乡玉米叶，得知含氟量为４３．９４－１６６．１ｍｇ／ｋｇ，对照样品树新林场玉米叶的含氟均值为１３．１５ｍｇ／ｋｇ，广武乡的玉米受到了严重的氟污染，农作物减产严重。     

小清河水体和沿岸地下水中有机污染物的监测及其毒性分析

本文对小清河水体和沿岸地下水中的有机污染物进行了色－质联用分析，共检出有机污染物１３类９３种。并对其毒性效应进行了分析和评价。     

Determination of PAHs by On-Line Polarization Synchronous Fluorescence with HPLC

A novel analytical method has been established for on-line simultaneous determination of fluorene and acenaphthene,chrysene and benzo[a]anthracene (B[a]A) by polarization synchronous fluoromet.y (PSF) coupled to high performance liquid chromatography (HPLC). The detection limits were: 0.039, 0.046, 0.016 and 0.042 mgL-1 for fluorene, acenaphthene, chrysene and B[a]A, respectively. The proposed method has been successfisily applied to simultaneous determination of these PAHs in environmental air and marine sediment samples.     

EPA's monitoring program at Love Canal 1980

Summary As stated at the beginning of this paper conclusions reached thus far cannot be discussed in this paper. However, a great deal of information is available for examination.EPA displayed its ability to coordinate widely separated laboratories, both Federal and private, into a smooth working team in a very short period of time. A very comprehensive study plan was also developed and implemented quickly. EPA was fortunate to have already had GCA under contract when the emergency arose. In no small part the success of the field effort was due to the managerial and technical abilities of the GCA team.Within a period of 6 weeks a plan was developed, a prime contractor retained, subcontractors hired, and field activities begun. Within a period of 3 months in excess of 8600 field samples were collected and over 12,000 field and QC samples were analyzed. During this same period 2 major data systems were developed, debugged, and placed into operation.In short this EPA project was probably the most comprehensive multimedia field project ever attempted by EPA and certainly the data is being subjected to the most strenuous quality control measures ever imposed by this Agency. The entire program is presently under peer review and the results are being prepared for publication by EPA Headquarters.Note. Originally intended to be published as part of the special issue on Exposure Monitoring: An International Workshop (Las Vegas, Nevada, October 19–22, 1981).     

Determination of Trace Organochlorinated Pesticides and Polychlorinated Biphenyls in Water

A modified steam distillation liquid-liquid extraction (SDE) device is developed for the enrichment of trace organochlorinated pesticides (OCPs) and polychlorinated biphenyls (PCBs) in up to one litre of water samples. One ml of n-hexane is sufficient to extract the analytes. The extract can be analysed directly by a capillary gas chromatography-electron capture detector. The recoveries range from 84.6 to 102.3% for OCPs and 80.5 to 106.2% for PCBs, respectively. Matrice materials such as lipids and humic substances were removed by the SDE method from the extract and no further cleanup and concentration steps were needed.     

Preliminary studies of a fast screening method for polycyclic aromatic hydrocarbons in soil by using solvent microextraction-gas chromatography

Solvent microextraction (SME) was applied to the extraction of polycyclic aromatic hydrocarbons (PAHs) from spiked and real environmental soil samples with different matrices. Soil sample was mixed with 7 mL of acetone and 14 mL of water to allow partitioning of the PAHs from the soil to the liquid phase. A 2 microL octane drop suspended from a microsyringe needle tip was then immersed into the stirred solution-soil mixture for extraction. After an 11 min extraction, the octane drop was withdrawn into the syringe and injected directly into the GC for identification and quantification. The whole analysis procedure took 27 min, with an extraction time of 11 min, and a GC separation time of 16 min. A second extraction could be undertaken whilst the GC is running, hence the GC run time currently limits the sample throughput. In this method, a small amount of organic solvent was used for the extraction process, which produced little waste. The limits of detection for lower molecular weight (< 230) PAHs range from 0.13 to 0.36 mg kg-1, and for higher molecular weight (> 250) PAHs are estimated to be between 0.5 and 1.0 mg kg-1, with RSD values generally under 20%. Due to the small volumes of organic solvent used, the consumable cost per extraction is only US$ 0.12. This is the first report of the application of SME to solid samples, and the first report of the use of SME for the analysis of PAHs.