巯基棉纤维制备方法的研究

巯基棉富集分离技术现已广泛的应用于天然水、工业废水、土壤、沉积物、岩石、矿物、动植物、粮食及食品等各类环境样品中的钻、镍、锌、镉、铅、铟,钨、铜、银、锡、铋、锑、汞、砷、硒、碲、金、钯、铂等二十种痕量元素的分离和测定。     

重庆西部农业区大气沉降特征及其对地表的影响

从2009年4月至2010年4月,在重庆西部农业区采集了50个大气干、湿沉降样品,分别测试干、湿沉降样品中K、Ca、Mg、N、P、S、Fe、As、Cd、Cr、Cu、Hg、Ni、Zn、Pb、B、Mo、Mn 18种元素的含量,计算各元素的年沉降通量。研究发现,重庆西部农业区各元素年沉降通量均低于重庆主城区和成都经济区。采用富集因子分析得出,S、Cd、N、Pb、P、Hg、Mo、Zn、Cr、As明显受人为活动影响,其中S、Hg、As、Pb是典型的燃煤元素,Cd、Cr、Zn主要来源于工业排放、汽车尾气等,N、P与农业施肥密切相关。相关性分析表明,大气沉降输入Hg引起土壤中Hg含量显著增加,大气沉降输入S引起地表水中SO2-4浓度显著升高。     

不同粒度飞灰中16种微量元素的含量分布

研究了不同粒级的燃煤飞灰中的Ｂａ、Ｂｅ、Ｃｄ、Ｃｒ、Ｃｕ、Ｈｇ、Ｌｉ、Ｍｎ、Ｎｉ、Ｐｂ、Ｓｒ、Ｔｉ、Ｖ、Ｚｎ、Ｚｒ元素的含量分布,煤中元素的含量比及富集因子。     

环境污染与防治一九八二年总目录

环境管理期数页数、.产、‘了、,了、,矛、万J、少、少、月了、.户、.了、.夕、20 no,d Jq‘矛.、Z‘、产r、了‘、矛才、J‘、沪‘、子‘、矛‘、J宁‘、了通、了吸、、、J产、口产、吸了、.声、.产、月了‘、产、.产血、矛、.产、.2、、j,土,上1上1上O自n乙d︸J斗‘任八h八b八b户r‘、护厅、尹‘.夕r、产忆、了‘、了气、矛t、户口、了.、了召、尸‘、关于《浙江省防治环境污染暂行条例》的执行情况·············································……孙健如排污收费与价值规律····…     

农药微生物降解的研究现状与发展策略

本文在农药降解菌的富集分离及农药微生物降解的途径，特别在微生物产生的农药降解酶和农药微生物降解基因操作方面对农药微生物降解的研究现状作了简要综述，提出了农药微生物降解的研究趋势。联系地址：中国科学院广州地球化学研究所，广州五山，５１０６４０津、环草隆、三氯醋酸、氯苯胺灵等。芽孢杆菌属（Ｂａｃｉｌｌｕｓ）：ＤＤＴ、ｒ－ＢＨＣ、艾氏剂、狄氏剂、异狄氏剂、七氯、苯硫磷、对硫磷、甲基对硫磷、杀螟松、毒杀芬、茅草枯、三氯醋酸、利谷隆、灭草隆、毒旁定。节细菌属（Ａｒｔｈｒｏｂａｃｔｅｒ）：ＤＤＴ、艾氏剂、异狄氏剂、七氯、草多索、马拉硫磷、二嗪农、２，４－Ｄ、２甲４氯、茅草枯、三氯醋酸、毒莠定、西玛津、味哺丹［８］。棒状杆菌属（Ｃｏｒｙｎｂｏａｃｔｅｒｉｕｍ）：ＤＤＴ、２，４－Ｄ、２甲４氯、茅草枯、二硝甲酚、百草枯、草枯醚。无色杆菌属（Ａｃｈｒｏｍｏｂａｃｔｅｒ）：ＤＤＴ、西维因、２，４－Ｄ、２甲４氯、２，４，５－Ｔ、氯苯胺灵。土壤杆菌属（Ａｇｒｏｂａｃｔｅｒｉｕｍ）：ＤＤＴ、氯苯胺灵、茅草枯、三氯醋酸、毒莠定。黄杆菌属（Ｆｌａｖｏｂａｃｔｅｒｉｕｍ）：对硫磷、甲基对硫磷、马拉硫磷、二嗪农、毒死蜱、２，４－Ｄ、２甲４氯、     

国内含氰废水处理述评

在冶金、化工、选矿、金属加工、化纤、塑料、电镀、农药、仪表、煤气、炼焦、炼油和热处理等行业排出的工业废水中,氰化物含量往往超过国家允许的排放标准.为了处理含氰废水,我们于八○年九月十二日至十月廿三日,历时四十余天,先后去江西、湖南、湖北、陕西、北京、山东、江苏、     

宁波市土壤环境背景值及其分异特征

本文介绍了土壤中铜、铅、锌、镉、汞、铬、镍、锰、钴、铁、氟、砷、钒、硒等十四个微量元素的背景值,并对其在不同土类、不同母质、不同土层中的分异进行了论述。对今后宁波市制定发展规划、国土整治、工农业合理布局等提供了重要的科学依据。     

北京市PM2.5污染特征 、来源分析及其重金属健康风险评价

分析了2016年北京市的PM_(2.5)及其中的Zn、Pb、Mn、Cu、Cr、As、Ni、Cd、Sb、Co、V、Ba、Al、Fe、Mg、Ti、Ca、S 18种元素含量,并对重金属As、Cr、Pb、Cd、Ni、Mn、Cu和Zn进行了相应的健康风险评价。结果表明:PM_(2.5)质量浓度为14.63～206.35μg/m~3,年平均值为74.00μg/m~3,超过《环境空气质量标准》(GB 3095—2012)二级标准(35μg/m~3)1倍多;PM_(2.5)中S、Zn、Sb、Pb和Cd的富集程度较高,主要来源于机动车尾气排放、燃煤和工业活动;Mn、Pb、Cr、Zn、Cu、As、Cd、Ni 8种重金属对儿童、成人女性、成人男性的非致癌总风险均小于1,不存在非致癌风险;As、Cd、Cr和Ni 4种重金属的致癌风险为1.94×10~(-7)～6.04×10~(-5),均小于10~(-4),部分重金属可能存在潜在致癌风险,主要是As和Cr存在潜在致癌风险。     

株洲市公园土壤重金属污染现状及评价

随着城市化和工业化进程的推进,城市及其周边地区已受到明显的重金属污染.研究了株洲市4个公园5个土壤样品的重金属污染特征,研究表明,Cu、Zn、Cr、Cd、Pb、Ni、Hg、As的平均值分别为52.43、129.15、66.37、0.55、48.82、30.36、0.08、4.80mg/kg.以2003年株洲市土壤重金属...     

头孢菌素制药行业水污染物特征成分谱解析

以某大型头孢菌素制药企业为研究对象,通过测定生产废水中常规污染物、金属污染物和有机污染物等,以开展水污染物的特征成分谱解析。结果表明,参照《发酵类制药工业水污染物排放标准》(GB 21903—2008)、《地表水环境质量标准》(GB3838—2002),发现头孢菌素制药行业的水污染物特征成分谱为挥发酚、COD、石油类、总氮、氨氮、总磷、Zn、Mn、Cr、Se、甲基异丁基酮、乙酸乙酯、四氢呋喃、甲苯、丙酮、二苯基甲醇、4-甲基苯酚、3-甲基苯酚、乙醇、苯酚、α-苯基苯甲醇乙酸酯、乙酸甲酯、苯甲酮等;头孢菌素制药废水中大部分金属以溶解态形式存在,但总体来说悬浮态金属的去除率比溶解态金属高;在该行业的水污染物减排工艺选择时,要关注总磷,总氮,溶解态Zn、Mn、Cr、Se的减排,并要考虑甲基异丁基酮、乙酸乙酯、四氢呋喃等难生物降解有机物的可去除性。     

Persistence and dissipation kinetics of trifloxystrobin and tebuconazole in onion and soil

The persistence and dissipation kinetics of trifloxystrobin and tebuconazole on onion were studied after application of their combination formulation at a standard and double dose of 75 + 150 and 150 + 300 g a.i. ha^?1. The fungicides were extracted with acetone, cleaned-up using activated charcoal (trifloxystrobin) and neutral alumina (tebuconazole). Analysis was carried out by gas chromatograph (GC) and confirmed by gas chromatograph mass spectrometry (GC-MS). The recovery was above 80% and limit of quantification (LOQ) 0.05 mg kg^?1 for both fungicides. Initial residue deposits of trifloxystrobin were 0.68 and 1.01 mg kg^?1 and tebuconazole 0.673 and 1.95 mg kg^?1 from standard and double dose treatments, respectively. Dissipation of the fungicides followed first-order kinetics and the half life of degradation was 6–6.6 days. Matured onion bulb (and field soil) harvested after 30 days was free from fungicide residues. These findings suggest recommended safe pre-harvest interval (PHI) of 14 and 25 days for spring onion consumption after treatment of Nativo 75 WG at the standard and double doses, respectively. Matured onion bulbs at harvest were free from fungicide residues.     

Sorption and Desorption Behavior of Chloroanilines and Chlorophenols on Montmorillonite and Kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Field and laboratory studies of the fate and enantiomeric enrichment of venlafaxine and O-desmethylvenlafaxine under aerobic and anaerobic conditions

The stereoselectivity of R,S-venlafaxine and its metabolites R,S-O-desmethylvenlafaxine, N-desmethylvenlafaxine, O,N-didesmethylvenlafaxine, N,N-didesmethylvenlafaxine and tridesmethylvenlafaxine was studied in three processes: (i) anaerobic and aerobic laboratory scale tests; (ii) six wastewater treatment plants (WWTPs) operating under different conditions; and (iii) a variety of wastewater treatments including conventional activated sludge, natural attenuation along a receiving river stream and storage in operational and seasonal reservoirs. In the laboratory and field studies, the degradation of the venlafaxine yielded O-desmethylvenalfaxine as the dominant metabolite under aerobic and anaerobic conditions. Venlafaxine was almost exclusively converted to O-desmethylvenlafaxine under anaerobic conditions, but only a fraction of the drug was transformed to O-desmethylvenlafaxine under aerobic conditions. Degradation of venlafaxine involved only small stereoisomeric selectivity. In contrast, the degradation of O-desmethylvenlafaxine yielded remarkable S to R enrichment under aerobic conditions but none under anaerobic conditions. Determination of venlafaxine and its metabolites in the WWTPs agreed well with the stereoselectivity observed in the laboratory studies. Our results suggest that the levels of the drug and its metabolites and the stereoisomeric enrichment of the metabolite and its parent drug can be used for source tracking and for discrimination between domestic and nondomestic wastewater pollution. This was indeed demonstrated in the investigations carried out at the Jerusalem WWTP.     

Synthesis and characterization of m- and p-methylbenzyl-mercapturic acids derived from m- and p-xylenes

Chemical synthesis and physical properties of two mercapturic acids suggested as urinary metabolites of m- and p-xylenes ace described. These compounds may be used for the identification and quantivative determination by high-performance liquid chromatography of the corresponding mercapturic acids in urine.     

Levels of PCDDs and PCDFs in products and effluent from the Swedish pulp and paper industry and chloralkali process

Within the Swedish Dioxin Survey various samples from the pulp and paper industry and the chloralkali process have been analyzed by congener specific analytical methods. In addition to the generally discussed “bleaching pattern” of the tetrachlorinated congeners, these samples also contained higher chlorinated congeners like hexa-CDDs, hepta-CDFs, octa-CDD and octa-CDF. Consequently it is recommended that samples from the pulp industry should be analyzed for all PCDDs and PCDFs (tetra- through octa-). Counted as Nordic Toxic Equivalents (NTEQ), the recycled pulp samples had the highest contamination level followed by TMP, unbleached sulfite and bleached softwood and hardwood. In addition to the bleaching process, various chemicals used in the pulping, bleaching and wastewater treatment can contribute to the contamination.     

Copper-catalyzed chlorination and condensation of acetylene and dichloroacetylene

The chlorination and condensation of acetylene at low temperatures is demonstrated using copper chlorides as chlorinated agents coated to model borosilicate surfaces. Experiments with and without both a chlorine source and borosilicate surfaces indicate the absence of gas-phase and gas-surface reactions. Chlorination and condensation occur only in the presence of the copper catalyst. C₂ through C₈ organic products were observed in the effluent; PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed that is consistent with the observed product distributions. Similar experiments with dichloroacetylene indicate greater reactivity in the absence of the copper catalyst. Reaction is observed in the gas-phase and in the presence of borosilicate surfaces at low temperatures. The formation of hexachlorobenzene is only observed in the presence of a copper catalyst. PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed for the formation of hexachlorobenzene from dichloroacetylene.     

Sorption and desorption of Cu and Cd by macroalgae and microalgae

The sorption and desorption of Cu and Cd by two species of brown macroalgae and five species of microalgae were studied. The two brown macroalgae, Laminaria japonica and Sargassum kjellmanianum, were found to have high capacities at pHs between 4.0 and 5.0 while for microalgae, optimum pH lay at 6.7. The presence of other cations in solution was found to reduce the sorption of the target cation, suggesting a competition for sorption sites on organisms. Sorption isotherms obeyed the Freundlich equation, suggesting involvement of a multiplicity of mechanisms and sorption sites. For the microalgae tested, Spirulina platensis had the highest capacity for Cd, followed by Nannochloropsis oculata, Phaeodactylum tricornutum, Platymonas cordifolia and Chaetoceros minutissimus. The reversibility of metal sorption by macroalgae was examined and the results show that both HCl and EDTA solutions were very effective in desorbing sorbed metal ions from macroalgae, with up to 99.5% of metals being recovered. The regenerated biomass showed undiminished sorption performance for the two metals studied, suggesting the potential of such material for use in water and wastewater treatment.     

Aerobic and anaerobic degradation of profluralin and trifluralin

Abstract

The degradation of profluralin [N‐(cyclopropylmethyl)‐α,α,α‐trifluoro‐2,6‐dinitro‐N‐propyl‐]p‐toluidine] and trifluralin (α,α,α‐trifluoro‐2,6‐dinitro‐N,N‐dipropyl‐p‐toluidine) was studied under aerobic and anaerobic soil conditions. Three soils (Goldsboro loamy sand, Cecil loamy sand, Drummer clay loam) were each treated with 1 ppmw herbicide; anaerobic conditions were maintained by flooding. Soil samples were extracted monthly and subjected to TLC analysis. No degradation was detected in sterile controls. Aerobic degradation of both herbicides was greatest in the Cecil loamy sand soil over the entire incubation period. Degradation of profluralin in Cecil soil under aerobic conditions was 86 percent after 4 months with three products detected; 83 percent of the trifluralin was degraded with two products detected. Anaerobic degradation accounted for 72 percent of the profluralin and 78 percent of the trifluralin after 4 months. Degradation of both herbicides increased with incubation time for the first 3 months and decreased slightly thereafter. Generally there was more extensive degradation (percent and in number of products formed) of profluralin than trifluralin under the conditions tested. More degradation products were detected for both herbicides under aerobic conditions than under anaerobic conditions.     

Uptake and translocation of metformin, ciprofloxacin and narasin in forage- and crop plants

Transfer of bioactive organic compounds from soil to plants might represent animal and human health risks. Sewage sludge and manure are potential sources for bioactive compounds such as human- and veterinary drugs. In the present study, uptake of the anti-diabetic compound, metformin, the antibiotic agent ciprofloxacin and the anti-coccidial narasin in carrot (Daucuscarota ssp. sativus cvs. Napoli) and barley (Hordeumvulgare) were investigated. The pharmaceuticals were selected in order to cover various chemical properties, in addition to their presence in relevant environmental matrixes. The root concentration factors (RCF) found in the present study were higher than the corresponding leaf concentration factors (LCF) for the three test pharmaceuticals. The uptake of metformin was higher compared with ciprofloxacin and narasin for all plant compartments analyzed. Metformin was studied more explicitly with regard to uptake and translocation in meadow fescue (Festucapratense), three other carrot cultivars (D.carota ssp. sativus cvs. Amager, Rothild and Nutri Red), wheat cereal (Triticumaestivum) and turnip rape seed (Brassicacampestris). Uptake of metformin in meadow fescue was comparable with uptake in the four carrot cultivars (RCF 2-10, LCF approximately 1.5), uptake in wheat cereals were comparable with barley cereals (seed concentration factors, SCF, 0.02-0.04) while the accumulation in turnip rape seeds was as high as 1.5. All three pharmaceuticals produced negative effects on growth and development of carrots when grown in soil concentration of 6-10 mg kg⁻¹ dry weight.     

Sources and distribution of polychlorinated-dibenzo-p-dioxins and -dibenzofurans in soil and sediment from the Yellow Sea region of China and Korea

Polychlorinated-dibenzo-p-dioxins and -dibenzofurans (PCDD/Fs) were measured in soils and sediments from the Yellow Sea region. Korean soils and sediments mostly contained detectable PCDD/Fs and showed a widespread distribution among locations. Soil and sedimentary PCDD/Fs from China were comparable to or less than those in Korea. The patterns of relative concentrations of individual congeners in soils were different between the two countries, but similar in sediments. Sources of PCDD/Fs in China and Korea were found to be independent of each other and their distributions reflected matrix-dependent accumulation. Spatial distribution indicated some point sources in Korea while Chinese sources were more widespread and diffuse. PCDD/Fs measured in the coastal areas of the Yellow Sea were comparable to or less than those previously reported in for eastern Asia. However, ∑TEQs in soils and sediments were near to or, in some cases exceeded environmental quality guidelines.