Trace analysis of parabens preservatives in drinking water treatment sludge,treated, and mineral water samples

Parabens have been widely used as antimicrobial agents, mainly in food products, pharmaceuticals, and cosmetics. Although they are known as safe preservatives, they also cause some harm to human health, which has been discussed lately. Therefore, the aim of this study was to evaluate the occurrence of nine parabens (including isomers) in mineral and drinking waters, besides in drinking water treatment sludge (DWTS) samples with determination by liquid chromatography tandem mass spectrometry (LC-MS/MS). Both methods solid phase extraction (SPE) and QuEChERS were validated. Calibration curves showed a correlation coefficient of 0.99 for all compounds. LOQ values ranged from 0.04 to 4 μg L^?1 in aqueous matrices and from 5 to 500 ng g^?1 in DWTS. Recoveries between 70 and 115% were reached with RSD below 20% for all compounds in SPE whereas recoveries between 62 and 119% were found with RSD below 20% for almost all compounds in QuEChERS. Matrix effect had low values (<?20%); it was only above 20% for methylparaben in the SPE and for pentylparaben in the QuEChERS. Using a quick and simple extraction procedures with SPE, QuEChERS, and LC-MS/MS analyses, these methods proved to be selective and sensitive. They were successfully applied to real samples (treated water, mineral water, and sludge), and methylparaben was detected at concentration levels below 0.242 μg L^?1 in mineral and treated water samples and 10 ng g^?1 in DWTS samples.     

Uncertainty health risk assessment and regional control of drinking water: a case study of Hanyuan County,southwest mountainous area,China

Environmental Science and Pollution Research - To evaluate the health risks of drinking water in Hanyuan County, 96 samples of peripheral drinking water were collected from 30 sites in the area....     

Formation of halogenated acetaldehydes, and occurrence in Canadian drinking water

Controlled laboratory chlorination of acetaldehyde (ACD) under typical drinking water conditions (pH 6.7, 7.6 and 8.8, and temperature 4 degrees C and 21 degrees C) revealed that the formation of chloral hydrate (CH), the most common halogenated acetaldehyde (HAs), increased with contact time (0-10 days). However, at increased pH and temperature, CH reached maximum levels and subsequently broke down partially to chloroform and other unidentified compounds. After 10 days contact time, a maximum of 63% (molar) of the initial ACD consumed were converted into CH or chloroform (TCM). Various surveys of drinking water systems indicated that ACD is not the only precursor of CH. A suite of aldehydes (including ACD), and chlorinated disinfection by-products (including TCM and CH) were found in most distribution systems. The levels of bromide in source water impacted speciation of HAs. In addition to CH, brominated and other mixed (Cl/Br) acetaldehydes were detected in most samples; the speciation of HAs and THMs followed comparable trends. Similar to chloroform for trihalomethanes, CH contributed from as low as 5% to up to 60% of the total HAs. The bromine incorporation factors (BIF) in THMs and HAs were shown to increase with increasing bromide ion concentrations in the source water. Brominated THMs are more readily formed than their HA analogues; in fact, BIF values for THMs were 2-3 times higher than for the HAs. It was found that HAs may be as high as THMs in some drinking waters. As a result, the determination of the other target HAs, in addition to CH, is necessary for a better assessment of the pool of disinfection by-products in drinking water.     

Occurrence of sulfonamide antimicrobials in private water wells in Washington County, Idaho, USA

Samples from six private wells formerly used as sources for drinking water by the residents of Washington County (Weiser, Idaho) were collected to assess the impact of a nearby confined animal feeding operation (CAFO) on the quality of the local groundwater. All six samples were found contaminated by two veterinary antimicrobials, sulfamethazine (at concentrations from 0.076 to 0.22 μg/l) and sulfadimethoxine (at concentrations from 0.046 to 0.068 μg/l). These groundwater samples also contained elevated concentrations of nitrate and ammonium. Three of the sampled wells have nitrate levels that exceeded the maximum contaminant level set by the US Environmental Protection Agency for drinking water, with nitrate concentration as high as 39.1 mg/l. All but one well showed nitrate, which instead contained ammonium at 1.22 mg/l. Analysis of the nitrate and ammonium in these samples by isotopic ratio mass spectrometry indicated δ¹⁵N characteristic of an animal or human waste source. Results from this study underscore the role of CAFO as an important source of antibiotic contamination of groundwater.     

Environmental mercury contamination of an artisanal zinc smelting area in Weining County, Guizhou, China

To investigate the extent of Hg contamination due to artisanal Zn smelting activities in Weining County, northwestern Guizhou, China, total Hg and methyl mercury (MeHg) concentrations in soil and surface water were determined. Samples of corn plants growing in the study area were also collected for total Hg analysis. A high geometric mean Hg emission factor of 75gHgt(-1)Zn was estimated and significantly elevated total gaseous mercury (TGM) concentrations were found in the atmosphere adjacent to the Zn smelting sites, ranging from 30 to 3814ngm(-3). Total Hg and MeHg concentrations in topsoil samples ranged from 62 to 355microgkg(-1) and from 0.20 to 1.1microgkg(-1), respectively. Total Hg Concentrations in corn plant tissues increased in the order of grains相似文献   

Response of bacterial communities to mining activity in the alpine area of the Tianshan Mountain region,China

Environmental Science and Pollution Research - Anthropogenic activities, such as mining, influence soil bacterial community composition and microbial distributions. In the current study, the...     

Screening of endocrine-disrupting phenols, herbicides, steroid estrogens, and estrogenicity in drinking water from the waterworks of 35 Italian cities and from PET-bottled mineral water

We investigated contamination by endocrine-disrupting chemicals in drinking water from 35 major Italian cities and five popular Italian brands of bottled mineral water. The quality of Italian drinking water was assessed by combing chemical analysis with bioassay to quantify specific estrogenic contaminants and to characterize the actual biological effect of the mixture of chemicals present in drinking water including the contribution of not targeted compounds. The selected contaminants were natural and synthetic steroid estrogens, alkylphenols and bisphenol A, linuron, triazine herbicides, and their metabolites. A specific analytical method was developed based on solid phase extraction of 1 L of water and concentration to 100 μL for quantification by electrospray ionization liquid chromatography tandem mass spectrometry, achieving quantification limits of 0.05–0.36 ng/L for herbicides and 0.64–7.70 ng/L for steroids and phenols. No steroid estrogens were detected in any of the samples, while bisphenol A and nonylphenols were detected in the ranges of 0.82–102.00 and 10.30–84.00 ng/L respectively. Herbicides and their degradation products, when present, were found from slightly above the quantification limits up to 49.91 ng/L, mainly from cities in northern Italy. Chemical analyses were complemented by the performance of a bioassay for the determination of the estrogenic activity in the extracts based on the transactivation of estrogen receptor α-transfected reporter HeLa-ERE-Luciferase-Neomycin cell line. Activity was generally low with maximum estrogenicity of 13.6 pg/L estradiol equivalents.     

DDT residues in water, sediment, domestic and indigenous biota from a currently DDT-sprayed area

DDT is used for indoor residual spraying (IRS) in Limpopo Province, northern South Africa to control malaria. Through IRS, DDT may reach the outdoor environment via dust and air and from possible spillages during application. In this area the local people consume domestic chickens, wild fish or birds. Fish from the river catchment and impoundments seem to be the major source of protein intake. Water, sediment and tissue samples from two such fish species, domestic chickens and wild birds (terrestrial and aquatic) from this DDT-sprayed area were analysed for DDT and metabolite residues. The samples contained p,p′-DDT, p,p′-DDD and p,p′-DDE residues, with the latter the most ubiquitous and in the highest concentrations. These findings raise concern that both water and food may be major routes of human exposure to DDT and metabolites, thereby posing possible adverse human health implications to the local communities.     

Trace metals in different species of mollusca, water and sediments from Taiwan coastal area

Since October 1994, a long-term program of Asia/Pacific Mussel Watch: Taiwan Regional Studies has been carried out. The results indicate that trace metal contents in mollusca varied among 30 different species and the environments (water and sediments) along the Taiwan coast. The orders of bioaccumulation of trace metals in mollusca were: Cu (over 200 microg/g), Thais clavigera > Isognomon legumen > Clibanarius rivescens > Crassostrea gigas; Zn (over 700 microg/g), Moruta granulata > C. gigas > Asiatica cypraea arabica > T. clavigera; Cd (over 5 microg/g), Trochus hanleyanus > Acanthopleura japonica > Nerita albicilla > Patella flexuosa; Pb (over 2 microg/g), P. flexuosa > C. gigas > T. hanleyanus > T. clavigera > C. gigas > Capiyulum mitella; Ni (over 10 microg/g), Meretrix lusoria > Philine sp. > Littoraria scabra > Tridacna squamosa > T. hanleyanus; Cr (over 30 microg/g), Littoraria undulata > T. hanleyanus > N. albicilla > Nerita chamaelor > M. granulata; As (over 20 microg/g), Perna viridis > L. scabra; and Sn (over 5 microg/g), P. viridis > L. undulata> C. mitella> C. gigas. Their seasonal and regional variations as well as their correlation are evaluated and discussed.     

Formation of disinfection by-products in chlorinated swimming pool water.

The formation of five volatile disinfection by-products (DBPs: chloroform, bromodichloromethane, chloral hydrate, dichloroacetonitrile, and 1,1,1-trichloropropanone) by the chlorination of the materials of human origin (MHOs: hair, lotion, saliva, skin, and urine) in a swimming pool model system was examined. Chlorination reactions took place with a sufficient supply of chlorine residuals (0.84 mg Cl2/l < total chlorine < 6.0 mg Cl2/l) in 300 ml glass bottles containing either ground water or surface water as a reaction medium at 30 degrees C and pH 7.0, for either 24 or 72 h. A longer reaction period of 72 h or a higher content of organic materials led to the increased formation of DBPs. Of the DBPs formed by the reaction, chloroform was a major compound found in both ground and surface waters. The formation of chloroform and bromodichloromethane per unit total organic carbon (TOC) concentration was suppressed when all types of MHOs were added to the surface water that already contained DBP precursors such as humic substances. However, the formation of dichloroacetonitrile was promoted, probably due to the increased degradation reactions of nitrogen-containing compounds such as urea and proteins of human origin. In conclusion, the materials of swimmers' origin including hair, lotion, saliva, skin, and urine add to the levels of DBPs in swimming pool water, and any mitigation measures such as periodic change of water are needed to protect swimmers from elevated exposures to these compounds.     

Photodegradation of naproxen in water under simulated solar radiation: mechanism,kinetics, and toxicity variation

The main objective of this study was to investigate the degradation mechanism, the reaction kinetics, and the evolution of toxicity of naproxen in waters under simulated solar radiation. These criteria were investigated by conducting quenching experiments with reactive oxygen species (ROS), oxygen concentration experiments, and toxicity evaluations with Vibrio fischeri bacteria. The results indicated that the degradation of naproxen proceeds via pseudo first-order kinetics in all cases and that photodegradation included degradation by direct photolysis and by self-sensitization via ROS; the contribution rates of self-sensitized photodegradation were 1.4 %, 65.8 %, and 31.7 % via ·OH, ¹O₂ and O₂ ^??, respectively. Furthermore, the oxygen concentration experiments indicated that dissolved oxygen inhibited the direct photodegradation of naproxen, and the higher the oxygen content, the more pronounced the inhibitory effect. The toxicity evaluation illustrated that some of the intermediate products formed were more toxic than naproxen.     

Formation of mutagenic activity during surface water preozonization and its removal in drinking water treatment

The influence of preozonization, coagulation and double layer filtration on formation and removal of mutagenic activity was studied using XAD-8 extracts collected from neutral and acidic solutions and assaying them in the Salmonella typhimurium microsomal assay.Preozonization of surface water produced direct acting frame shift mutagens which were adsorbed on XAD-8 from neutral solutions. This phenomenon was shown to be dependent on the ozone dose applied. Coagulation with different chemicals and subsequent direct filtration partially reduced the mutagenic activity.     

县域跨界水污染补偿机制在嘉兴市的探索

嘉兴市构建的县域跨界水污染补偿机制,不仅是一项流域水污染防治制度刨新,而且是浙江省跨行政区水污染补偿政策的重要支撑和有力保障.通过对大量数据的统计分析,提出了3种补偿标准,并运用跨界水污染补偿模型,模拟测算了2个市级断面和2个县级断面的补偿额.模拟测算结果不但能描绘出县域跨界水污染的现状,而且能够明确补偿对象和补偿额,对流域水质根本改善具有重要意义.     

龙形水系中心区水体富营养化评价与成因分析

龙形水系是北京奥林匹克公园内的主要景观水体,以再生水为主要补水水源.采用综合营养状态指数法对龙形水系中心区(简称中心区)水体富营养化状态进行评价.结果表明:(1)中心区水体全部为富营养状态,汛期的综合营养状态指数总体呈逐渐降低的趋势,即水体在汛期初期至中期为中度富营养,后期为轻度富营养;汛期结束后水质较差,综合营养状态指数上升,中心区水体达到重度富营养化状态.(2)再生水为中心区水体污染物的主要污染源,其TN、TP、COD和NH4+-N年输入量占各类污染物年总输入量的85％以上;在汛期,其主要污染物输入量占总输入量的70％以上.中心区水体在汛期没有明显的污染物集中输入现象.(3)中心区水体富营养化主要成因为氮磷等营养物质的输出量小于输入量,造成氮磷等营养物质大量累积.(4)在汛期,外界的适宜温度、饱和光照、水体的弱碱性和缓慢流速加大了中心区水体水华暴发风险.     

Microplastics in water,sediments, and fish at Alpine River,originating from the Hindu Kush Mountain,Pakistan: implications for conservation

Environmental Science and Pollution Research - Microplastics (MP) pollution is an emerging threat to life and the environment. These particles are not restricted to human-inhabited lands but also...     

Factors controlling groundwater quality in the Yeonjegu District of Busan City,Korea, using the hydrogeochemical processes and fuzzy GIS

The hydrogeochemical processes and fuzzy GIS techniques were used to evaluate the groundwater quality in the Yeonjegu district of Busan Metropolitan City, Korea. The highest concentrations of major ions were mainly related to the local geology. The seawater intrusion into the river water and municipal contaminants were secondary contamination sources of groundwater in the study area. Factor analysis represented the contamination sources of the mineral dissolution of the host rocks and domestic influences. The Gibbs plot exhibited that the major ions were derived from the rock weathering condition. Piper’s trilinear diagram showed that the groundwater quality was classified into five types of CaHCO₃, NaHCO₃, NaCl, CaCl₂, and CaSO₄ types in that order. The ionic relationship and the saturation mineral index of the ions indicated that the evaporation, dissolution, and precipitation processes controlled the groundwater chemistry. The fuzzy GIS map showed that highly contaminated groundwater occurred in the northeastern and the central parts and that the groundwater of medium quality appeared in most parts of the study area. It suggested that the groundwater quality of the study area was influenced by local geology, seawater intrusion, and municipal contaminants. This research clearly demonstrated that the geochemical analyses and fuzzy GIS method were very useful to identify the contaminant sources and the location of good groundwater quality.

     

Evaluation of HCH isomers and metabolites in soils, leachates, river water and sediments of a highly contaminated area

In this work we evaluate the contamination caused by HCH residues in the soil, leachates, river water and sediments of an industrial estate of the NW of Spain. We study the distribution of the isomers in the different matrices, analysing 37 soil samples, collected in eight points at several depths, six natural leachates, four river water samples and three river sediments. Soil and leachate samples present very high levels of HCH isomers, higher than the established by legislation, and some pesticides were also detected in the analysed river water whereas no pesticides were detected in the river sediments. The distribution of isomers was different depending on the matrix analysed. Some natural degradation products and also other organochlorine pesticides were detected in the samples analysed.     

Formation, characterization and release of non-extractable residues of [14C] -labeled organic xenobiotics in soils

The amount of non-extractable residues (NER) of organic xenobiotics in the soil can considerably exceed the amount of extractable residues which are accessible to normal residue analysis. The NER therefore present a burden to the soil, the toxicological and ecotoxicological potential of which is largely unknown. For the characterization of bound residues and their binding type, special solubilization methods such as supercritical fluid extraction are applied and experiments with radiolabeled model polymers are performed. Mineralization experiments with [¹⁴C] labeled xenobiotics in natural soil show that a total degradation is still also possible in the environment when in a bound form. Ecotoxicological effects of non-extractable residues may be recorded when their concentration is high, when the parent compound exhibits a high ecotoxicity and the applied detection method is sufficiently sensitive.     

Algal growth inhibition by river water pollutants in the agricultural area around Lake Biwa, Japan

An ecotoxicological study of river water discharged from the agricultural area around Lake Biwa was performed by using algal bioassays to guide chemical analysis. Water samples were collected once a week, at least, for 1 year starting in April 1997 and continuing until April 1998. The toxicities of the dissolved and particulate-adsorbed extracts of water samples were evaluated by the algal growth inhibition test and concentrations of individual pesticides were determined. Most of the river water that was collected during the periods when pesticides were applied to the paddy fields caused algal growth inhibition. Some extracts were found to contain herbicides (molinate, mefenacet, simetryn, or esprocarb) as major compounds. According to chemical assay and bioassay, simetryn was identified as the most toxic compound that caused algal growth inhibition.     

厕所污水回用脱色方法及机理研究

采用投加粉末活性炭对经膜生物反应器处理的厕所回用水（膜出水）进行脱色.对厕所回用水中色度物质的成分及分子量分布,对选定高效适用的活性炭及活性炭对厕所回用水中色度物质的去除机理进行了探讨.试验结果表明,使膜出水显色的物质是一类在紫外区有明显吸收或有特征吸收峰的有机物,且大部分物质分子量分布在6～60 KD的范围内.在选定有高效脱色效果的活性炭时,要综合考虑活性炭的亚甲基蓝吸附值和焦糖脱色率2个指标,其中焦糖脱色率有着更重要的意义.厕所回用水脱色是对其各个分子量区间颜色物质去除效果的总和.