供水管网生物膜有机物的二氯乙腈与二氯乙酰胺生成特性

在饮用水输配系统中,来源于管壁生物膜的有机物可能耗氯并生成消毒副产物(DBPs),包括二氯乙腈(DCAN)与二氯乙酰胺(DCAcAm)等高毒性含氮DBPs(N-DBPs).研究考察管网常见的细菌与其胞外聚合物(EPS)以及模拟管壁生物膜氯化与氯胺化后DCAN与DCAcAm的生成,并与天然有机物(NOM)和水源水有机物进行比较.结果显示,铜绿假单胞菌、恶臭假单胞菌与藤黄微球菌与氯反应生成的DCAN、DCAcAm浓度分别为1.48～2.02、0.21～0.38μg·mg~(-1)(mg~(-1)以TOC计),高于同反应条件下NOM的生成量;相比于氯化反应,3株细菌细胞氯胺化生成的DCAN与DCAcAm浓度明显更低.3株菌的EPS也是氯与氯胺化反应生成DCAN与DCAcAm的前体物,且其氯胺化反应生成的DCAcAm浓度高于氯化反应生成的.与NOM、水源水相比,模拟管壁生物膜氯化后生成的N-DBPs与三氯甲烷(TCM)浓度比更高,表明生物膜有机物比NOM与水源水有机物更倾向生成DCAN与DCAcAm类N-DBPs,且模拟管壁生物膜氯胺化的DCAcAm生成量高于氯化反应的,说明管壁生物膜有机物是供水管网系统中DCAN与DCAcAm类N-DBPs的重要前体物.     

Concentration and Distribution of Persistent Organic Pollutants (POPs) in Harbour Dredging Sediments: A Pilot Study Using a Statistical Approach for a More Efficient Characterisation and Management

The Italian guidelines concerning the dumping of dredgingmaterials implies chemical, physical and microbiologicalcharacterisation of dumping sediments collected through aspecific sampling strategy.POP's such as PCB's and organochlorine pesticides, areconsidered as priority pollutants in all the InternationalConventions for the protection of the marine environment, inconsequence of their persistence, toxicity and bioaccumulation capacity.In the present article the concentrations and distribution ofPCB's and organochlorine pesticides in dredging sediments ofPiombino harbour (northern Thyrrenian sea) were investigates.The results showed high POP's concentrations in all the studiedareas. The maximum values were: 3.94 mg kg^-1 dry weight for PCB's(IUPAC Nos. 28; 52; 101, 118; 137; 153; 180; 209); 2.04 mg kg^-1 d.w.for HCH's (-, -, - and -hexachlorocyclohexane isomers); 0.28 mg kg^-1 d.w. for DD's (DDT + DDE + DDD).Subsequently, the data related to each pollutant were treatedwith statistical tests, in order to verify how well the samplingstrategy is able to represent the distribution of contaminantsin the dredging area. Finally, management strategies werederived for the studied dredging sediments.     

固相微萃取-毛细管气相色谱法快速同步分析水中有机氯及有机磷农药

固相微萃取是一种快速、简便,集萃取浓缩进样于一体的样品前处理技术,具有分析时间短、灵敏度高、无需有机溶剂的优点.用固相微萃取富集水中8种有机氯及7种有机磷农药,毛细管气相色谱ECD检测器分离分析,整个分析过程只需26min,检出限可达0.002～1μg/L,已用于地表水中有机氯及有机磷农药含量的测定.     

CHLORINATED HYDROCARBON (HCB, DDTs AND PCBs LEVELS IN CETACEANS STRANDED ALONG THE ITALIAN COASTS: AN OVERVIEW

Concentrations of HCB, DDTs and PCBs in the tissues andorgans of cetaceans ( Stenella coeruleoalba, Tursiops truncatus, Balaenoptera physalus, Steno bredanensis}, Grampus griseus} and Globicephala melaena) strandedalong the Italian coasts in the period 1987–1993 are reported. The values are compared between speciesand between specimens of the samespecies. Chlorinated hydrocarbon (CH) levels were found toincrease in relation to the quantity andtype of lipids in each tissue and organ. Differences inaccumulation encountered in the differentspecies are principally due to different feeding habitats.Remarkable differences found between malesand females of each species confirm that during gestation andlactation, females undergo disintoxication by passing much of their total burden of CHs to their young.     

自然界中铁硫化物矿物对含氯有机化合物降解作用

含氯有机化合物被广泛用于工农业生产和人们的日常生活中 ,对环境污染也日益严重。缺氧环境下对含氯有机化合物的非生物转化是自然界自我调控的过程之一 ,而广泛存在于这一环境中的铁硫化物矿物在这一过程中起着重要的作用。本文主要从反应机理角度回顾了铁硫化物矿物作为有机氯污染物主体还原剂的研究现状 ,并对进一步研究中可能存在的问题及研究重点提出了具体的建议。     

生物过滤饮用水深度处理:机遇与挑战

源水水质的恶化给传统的饮用水处理工艺带来了挑战.生物过滤是饮用水消毒输配之前管理、维护及增强颗粒滤料表面生物活性以去除有机和无机物的过程.由于具有高效、低成本等优点，生物过滤在饮用水深度处理工艺中逐渐得到广泛的应用.本文综述了生物过滤在饮用水处理过程中对水中溶解性有机质（消毒副产物前体物）的去除、微量污染物的削减、嗅味化合物及氨氮的去除等.此外，针对生物过滤在水深度处理过程中存在的问题，本文详细讨论了含氮消毒副产物前体物的生成、低温下生物过滤效能下降等挑战，并提出了今后需要研究的问题.     

化工园区生化出水氯代烃污染物的臭氧氧化降解

以化工园区污水处理厂生化出水为背景水样,考察了臭氧氧化对2,4,6-三氯酚、氯苯、1,2-二氯苯、对硝基氯苯、四氯酞酸5种特征氯代烃污染物的降解效果,并对其降解动力学进行了分析。实验结果表明:臭氧对2,4,6-三氯酚和氯苯的降解效果最好,反应30 min时的去除率均接近100%,其次为1,2-二氯苯和对硝基氯苯,反应30 min时的去除率分别为95.7%和36.0%,最差为四氯酞酸,反应30 min时的去除率仅为8.9%;臭氧对2,4,6-三氯酚和对硝基氯苯的降解符合零级动力学方程,对氯苯和1,2-二氯苯的降解符合一级动力学方程,对四氯酞酸的降解符合二级动力学方程。     

J市饮用水氯消毒副产物分析及其健康风险评价

J市位于太湖下游,其水源水质受上游和自身工农业发展的影响,有机物和氨氮浓度较高,氯消毒副产物及其引发的健康风险广泛受到关注.2012年5、8、10月以及2013年1月采样,使用气相色谱法分析了J市饮用水中4种三卤甲烷和5种卤乙酸的含量,发现自来水中三卤甲烷浓度占三卤甲烷与卤乙酸总和的88.1%以上,5月、8月和次年1月浓度较高(分别为39.34、50.37和28.02μg.L-1),10月浓度(19.19μg.L-1)较低,远高于卤乙酸的浓度(2.58～4.02μg.L-1).自来水煮沸3min后,三卤甲烷可去除92.3%以上,但卤乙酸会大幅度增加.基于EPA推荐的健康风险评价模型对经口摄取途径时氯消毒副产物的致癌和非致癌风险进行计算,发现化学致癌物质的健康风险为3.1×10-6～7.3×10-6,高于可接受风险水平1×10-6;煮沸后致癌物质的健康风险大幅度降低至7.9×10-7,低于可接受风险水平.煮沸后非致癌氯消毒副产物的健康风险由2.1×10-11显著升高至3.4×10-9,未超过10-5的风险管理参考值.     

Method to assess component contribution to toxicity of complex mixtures: Assessment of puberty acquisition in rats exposed to disinfection byproducts

A method based on regression modeling was developed to discern the contribution of component chemicals to the toxicity of highly complex, environmentally realistic mixtures of disinfection byproducts(DBPs). Chemical disinfection of drinking water forms DBP mixtures.Because of concerns about possible reproductive and developmental toxicity, a whole mixture(WM) of DBPs produced by chlorination of a water concentrate was administered as drinking water to Sprague–Dawley(S–D) rats in a multigenerational study. Age of puberty acquisition,i.e., preputial separation(PPS) and vaginal opening(VO), was examined in male and female offspring, respectively. When compared to controls, a slight, but statistically significant delay in puberty acquisition was observed in females but not in males. WM-induced differences in the age at puberty acquisition were compared to those reported in S–D rats administered either a defined mixture(DM) of nine regulated DBPs or individual DBPs. Regression models were developed using individual animal data on age at PPS or VO from the DM study. Puberty acquisition data reported in the WM and individual DBP studies were then compared with the DM models. The delay in puberty acquisition observed in the WM-treated female rats could not be distinguished from delays predicted by the DM regression model, suggesting that the nine regulated DBPs in the DM might account for much of the delay observed in the WM. This method is applicable to mixtures of other types of chemicals and other endpoints.