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1.
药品及个人护理用品(pharmaceutical and personal care products,PPCPs)在污水中广泛检出,低浓度的PPCPs即可对生态环境和人体健康产生不利影响,污水处理厂出水排放是水环境PPCPs的重要源.活性污泥和生物膜工艺是目前最常用的污水生物处理工艺,这两种工艺涉及的生化过程复杂,影...  相似文献   

2.
药物与个人护理品(pharmaceuticals and personal care products,PPCPs)作为一类与人们生产生活联系最为紧密的新型污染物在水环境中广泛检出,PPCPs在水环境中能够痕量存在,并在生物体内富集转化,对水生生态系统产生潜在的不利影响,其对水环境安全构成的潜在风险受到普遍关注.本文主要综述了我国地表水环境中PPCPs对生态环境的影响及生态风险评价的方法,分析了我国对水环境中PPCPs研究中存在的不足,提出了应对PPCPs风险评价的对策及建议.  相似文献   

3.
药物和个人护理用品(pharmaceuticals and personal care products,PPCPs)作为一类新兴的有机污染物备受研究者的关注,未被去除的PPCPs母体或转化/降解产物可能进入饮用水系统,威胁人体健康.本文分析了PPCPs在饮用水源、出厂水、供水管网和龙头水中的赋存状况,总结了饮用水厂各处理工艺对PPCPs的去除效果.PPCPs在饮用水系统中的浓度较低,一般在ng·L~(-1)到μg·L~(-1).饮用水厂处理工艺能有效去除特定PPCPs,其中氧化、活性炭及膜处理等深度处理工艺对PPCPs去除效果较好.加强对饮用水系统中PPCPs的来源控制、过程管理和末端监督等是将来的重要研究方向.  相似文献   

4.
药物和个人护理品简称(PPCPs)是一类具有潜在累积效果的环境污染物,其广泛分布于水体与土壤环境中.在土壤/沉积物中,PPCPs将发生一系列的物理、化学和生物作用,其中吸附是PPCPs在土壤/沉积物中极为关键的环境行为,将影响PPCPs在环境中的迁移转化及其对生物体的危害程度.重金属作为一类常见的无机污染物,它们的存在会影响PPCPs在土壤/沉积物表面的吸附行为,对土壤/沉积物吸附PPCPs的吸附效果造成不同影响.本文归纳总结了重金属存在时,PPCPs在土壤/沉积物中的吸附机理,综合探讨了PPCPs官能团组成、重金属离子类型、pH、离子强度和有机质等因素对PPCPs吸附的影响,并针对以往研究存在的问题进行了展望.  相似文献   

5.
<正>苯扎贝特(Bezafibrate)作为新兴污染物-药品和个人护理品(Pharmaceutical and personal care products,PPCPs)的一种,被广泛关注.其在污水处理厂的污水、地表水甚至是饮用水中常被检出[1].最新研究表明它对人体有类雌激素作用[2].目前,有人研究过光催化降解[1]和活性污泥转化[3]苯扎贝特的产物,但苯扎贝特在水环境中的生物降解途径及其中间产物的生态毒理效应尚不明确。  相似文献   

6.
药品和个人护理品(PPCPs)是一类新型有机污染物,随着生产和使用量的大量增加,越来越多的PPCPs进入土壤,对土壤生态环境和人体健康构成潜在威胁。文章根据现有研究,综述了国内外有关PPCPs在土壤中的吸附、生物降解、迁移、挥发等环境行为的研究进展,并分别评述了PPCPs对土壤生物(包括微生物、动物、植物)和人体的生态毒性效应。有关研究表明,PPCPs主要吸附于高有机质的土壤表层,低有机质亚表层土壤中PPCPs具有极高的迁移潜力;生物降解是PPCPs从土壤中去除的主要途径,受化合物自身结构和土壤理化特性的影响。高浓度PPCPs会对土壤生物(包括土壤微生物、动物和植物)产生急性生理生化甚至遗传毒性效应,最终可通过饮食危害人体健康,而PPCPs残留在土壤中的环境浓度通常较低,对土壤生物及人类极易造成慢性毒性损伤。目前有关土壤环境中PPCPs污染的研究尚处于初级阶段,今后可在真实土壤环境中痕量PPCPs的调查分析、迁移转化规律、生态健康风险及其代谢产物的行为和毒性等方面加强研究,以期为土壤环境中PPCPs生态风险的准确评估提供理论依据。  相似文献   

7.
药物及个人护理品(PPCPs)在水处理工艺中的迁移转化备受关注.二氧化氯(ClO_2)是一种常用的消毒剂,但水厂中二氧化氯制备工艺得到的常为复合二氧化氯(即ClO_2和Cl_2的混合物).目前,复合二氧化氯对PPCPs的去除方面研究还比较缺乏.本文研究了复合二氧化氯对16种常见PPCPs的降解效能,并与单独二氧化氯氧化进行比较.研究发现,PPCPs的降解效果与其化学结构密切相关.ClO_2可选择性氧化磺胺甲基嘧啶等含富电子基团的PPCPs,对甲硝唑等不含富电子基团的PPCPs降解能力有限,对咖啡因和扑米酮基本不降解.相比单独二氧化氯氧化,复合二氧化氯能促进萘啶酸、氟甲喹和对乙酰氨基酚的降解,但是对甲硝唑、二甲硝咪唑和避蚊胺的降解能力低于单独二氧化氯氧化.复合二氧化氯使用中亚氯酸盐生成量降低.  相似文献   

8.
药品与个人护理品在鱼体中的累积及代谢研究进展   总被引:1,自引:0,他引:1  
药品与个人护理品(pharmaceuticals and personal care products,PPCPs)作为一类广泛使用和具有特殊物理化学特性的新型环境污染物,能够在水环境中持续低浓度的存在,对水生生态系统具有潜在风险,已经引起了广泛的关注。鱼体内PPCPs的累积与代谢过程研究在PPCPs的生态风险评价中占据极其重要的地位。概述了PPCPs在鱼体内的分布,分析了影响PPCPs在鱼体内累积的因素如PPCPs的性质、组织差异、鱼的种类、不同的描述方法等,讨论了PPCPs的代谢机制,重点介绍了PPCPs在胆汁内的解毒机制和代谢产物,强调了胆汁应用的重要意义。最后,展望了PPCPs在鱼体内的累积和代谢这一研究领域的发展方向。  相似文献   

9.
药品和个人护理用品(PPCPs)对环境的污染现状与研究进展   总被引:24,自引:0,他引:24  
胡洪营  王超  郭美婷 《生态环境》2005,14(6):947-952
在过去的30多年中,有关有毒污染物的研究主要集中在工业化学物质和农药上。近5年多来,国外已经开始关注药品和个人护理用品(PPCPs)对环境的污染,但在我国还没有引起重视。国外的研究表明,合成麝香物质、显影剂、抗生素、雌激素、消炎止痛药、杀菌消毒剂等与人类生活密切相关的药品和个人护理用品在环境中普遍存在,但是其质量浓度通常非常低,多数情况下在ng/L~μg/L水平。粪便施肥和污水排放是PPCPs进入环境的主要途径。在常见的PPCPs中,抗生素和消炎止痛药在环境中检测出的频率最高,在地表水、地下水、饮用水、污泥、土壤等环境介质中,PPCPs在地表水中检测出的频率最高。目前关于PPCPs的研究主要集中在分析方法以及环境污染水平的调查,有关PPCPs在环境中的迁移转化规律,生态与健康风险以及PPCPs污染控制技术等方面的研究有待加强。  相似文献   

10.
吴春英 《环境化学》2013,(9):1674-1679
采用模拟生活污水,在相同的运行条件下,对比研究了膜-生物反应器(MBR)与序批式活性污泥法(SBR)对10种典型药品和个人护理品(PPCPs)的去除效果.研究结果表明,两种反应器对不同目标物PPCPs的去除效果存在一定的差异:MBR和SBR对甲氧苄氨嘧啶(TRM)和红霉素(ERY)的去除无明显差别;苏必利(SLP)和卡马西平(CBZ)在两反应器中均不能得到有效去除;但对于其他目标物,尤其是咖啡因(CAF)、酮洛芬(KTP)、避蚊胺(DEET),MBR的去除率明显高于SBR.总体上,MBR在出水的安全性和稳定性上存在着一定的优势.  相似文献   

11.
● A systematic framework was developed to identify i-PPCPs for landfill leachate. ● The wide-scope target analysis offered a basis for comprehensive i-PPCP screening. ● Source-specificity and representativeness analysis helped to refine i-PPCPs. ● Erythromycin, gemfibrozil and albendazole were identified as i-PPCPs for leachate. Identifying potential sources of pharmaceuticals and personal care products (PPCPs) in the environment is critical for the effective control of PPCP contamination. Landfill leachate is an important source of PPCPs in water; however, it has barely been involved in source apportionment due to the lack of indicator-PPCPs (i-PPCPs) in landfill leachates. This study provides the first systematic framework for identifying i-PPCPs for landfill leachates based on the wide-scope target monitoring of PPCPs. The number of target PPCPs increased from < 20 in previous studies to 68 in the present study. Fifty-nine PPCPs were detected, with median concentrations in leachate samples ranging from below the method quantification limit (MQL) to 41 μg/L, and 19 of them were rarely reported previously. A total of 29 target compounds were determined to be PPCPs of high concern by principal component analysis according to multiple criteria, including occurrence, exposure potential, and ecological effect. Coupled with source-specificity and representativeness analysis, erythromycin, gemfibrozil, and albendazole showed a significant difference in their occurrence in leachate compared to other potential sources (untreated and treated municipal wastewater and livestock wastewater) and correlated with total PPCP concentrations; these were recommended as i-PPCPs for leachates. Indicator screening procedure can be used to develop a sophisticated source apportionment method to identify sources of PPCPs from adjacent landfills.  相似文献   

12.
The application of appropriate advanced treat- ment process in the municipal wastewater treatment plants (WWTPs) has become an important issue considering the elimination of emerging contaminants, such as pharma- ceutical and personal care products (PPCPs). In the present study, the removal of 13 PPCPs belonging to different therapeutic classes by the sequential ultraviolet (UV) and ozonation process in a full-scale WWTP in Beijing was investigated over the course of ten months. Most of the target PPCPs were effectively removed, and the median removal efficiencies of individual PPCPs, ranging from -13% to 89%, were dependent on their reaction rate constants with molecular ozone. Noticeable fluctuation in the removal efficiencies of the same PPCPs was observed in different sampling campaigns. Nevertheless, the sequential UV and ozonation process still made a significant contribution to the total elimination of most PPCPs in the full-scale WWTP, by compensating for the poor or fluctuant removal performance of PPCPs by biologic treatment process.  相似文献   

13.
● A better risk assessment can combine the improved non-target analysis method. ● Multi-evidence is advised in molecular determination and risk-based prioritization. ● Combining omics, multi-endpoint EDA, and machine learning to assess product risks. The continuous input of various emerging contaminants (ECs) has inevitably introduced large amounts of transformation products (TPs) in natural and engineering water scenarios. Structurally similar to the precursor species, the TPs are expected to possess comparative, if not more serious, environmental properties and risks. This review summarizes the state-of-the-art knowledge regarding the integrated risk assessment frameworks of TPs of ECs, mainly involving the exposure- and effect-driven analysis. The inadequate information within existing frameworks that was essential and critical for developing a better risk assessment framework was discussed. The main strategic improvements include (1) non-targeted product analysis in both laboratory and field samples, (2) omics-based high-throughput toxicity assessment, (3) multichannel-driven mode of action in conjugation with effect-directed analysis, and (4) machine learning technology. Overall, this review provides a concise but comprehensive insight into the optimized strategy for evaluating the environmental risks and screening the key toxic products from the cocktail mixtures of ECs and their TPs in the global water cycle. This facilitates deciphering the mode of toxicity in complex chemical mixtures and prioritizing the regulated TPs among the unknown products, which have the potential to be considered a class of novel “ECs” of great concern.  相似文献   

14.
• A hydrophilic resin (GCHM) was facile synthesis and characterized. • Average absolute recovery of GCHM (75.6%) performs better than Oasis® HLB. • Detection limits of method (SPE-UPLC-MS/MS) ranged between 0.03 and 0.6 ng/L. • 22 PPCPs were determined in environmental waters ranging from 0.5 to 1590 ng/L. In this study, a hydrophilic resin named GCHM was fabricated based on poly(N-vinyl pyrrolidone-co-divinylbenzene), characterized, and applied as a solid-phase extraction (SPE) material. Up to 44 pharmaceuticals and personal care products (PPCPs) belonging to 10 classes were recovered in environmental water samples. Different variables affecting extraction, such as adsorbent amount, sample pH, and loading speed, were optimized. Under optimal conditions, the average absolute recovery of 44 PPCPs was 75.6% using GCHM, indicating a better performance than the commercial Oasis® HLB. SPE with home-made hydrophilic polymeric sorbent followed by ultra-performance liquid chromatography and tandem mass spectrometry was validated, and the method achieved good linearity (r2>0.991, for all analytes). In addition, the method detection limits of target compounds ranged from 0.03 to 0.6 ng/L. The developed method was applied to determine PPCPs in 10 environmental water samples taken from the Yangtze River, Huaihe River, and Taihu Lake, 1 groundwater sample from Changzhou in Jiangsu Province, 1 wastewater sample from Xiamen and 2 seawater samples from the Jiulong River in Fujian Province, China. In these samples, 22 compounds were determined at levels ranging from 0.5 to 1590 ng/L.  相似文献   

15.
The fate and removal of pharmaceuticals and personal care products (PPCPs) in wastewater treatment plants (WWTPs) has received great attention during the last decade. Numerous data concerning concentrations in the water phase can be found in the literature, however corresponding data from sludge as well as associated mass balance calculations are very limited. In the present study, the adsorbed and dissolved concentrations of 9 PPCPs were investigated in each unit of a WWTP in Beijing, China. Based on the calculation of mass balance, the relative mass distribution and removal efficiency of each target compound was obtained at each process. The amount of PPCPs entering into the WWTP ranged from 12 g·d–1 to 3848 g·d–1. Five target compounds (caffeine, chloramphenicol, bezafibrate, clofibric acid, and N,N-diethyl-meta-toluamide) were effectively removed, with rates of 57%–100%. Negative removal efficiencies were obtained for sulpiride, metoprolol, nalidixic acid, and carbamazepine, ranging from -19% to -79%. PPCPs mainly existed in dissolved form (≥92%) in both the raw influent and the final effluent. The sludge cake carried a much lower amount of PPCPs (17 g·d–1) compared with the discharged effluent (402 g·d–1). In A2/O treatment tanks, the anaerobic and anoxic tanks showed good performance for PPCPs removal, and the amount of adsorbed PPCPs was increased. The results reveal that both the dissolved and the adsorbed phases should be considered when assessing the removal capacity of each A2/O tank.  相似文献   

16.
• Isotope dilution method was developed for the determination of 27 PPCPs in water. • The established method was successfully applied to different types of water samples. • The correction effect of corresponding 27 ILSs over 70 d was investigated. • Benefit of isotopic dilution method was illustrated for three examples. Pharmaceuticals and personal care products (PPCPs) are a unique group of emerging and non-persistent contaminants. In this study, 27 PPCPs in various water samples were extracted by solid phase extraction (SPE), and determined by isotope dilution method using liquid chromatography coupled to tandem triple quadruple mass spectrometer (LC-MS/MS). A total of 27 isotopically labeled standards (ILSs) were applied to correct the concentration of PPCPs in spiked ultrapure water, drinking water, river, effluent and influent sewage. The corrected recoveries were 73%–122% with the relative standard deviation (RSD)<16%, except for acetaminophen. The matrix effect for all kinds of water samples was<22% and the method quantitation limits (MQLs) were 0.45–8.6 ng/L. The developed method was successfully applied on environmental water samples. The SPE extracts of spiked ultrapure water, drinking water, river and wastewater effluent were stored for 70 days, and the ILSs-corrected recoveries of 27 PPCPs were obtained to evaluate the correction ability of ILSs in the presence of variety interferences. The recoveries of 27 PPCPs over 70 days were within the scope of 72%–140% with the recovery variation<37% in all cases. The isotope dilution method seems to be of benefit when the extract has to be stored for long time before the instrument analysis.  相似文献   

17.
根据文献报道,我国地表水中已检出至少144种药物及个人护理用品(pharmaceuticals and personal care products,PPCPs),包括抗生素、激素、其他药物、个人护理品(personal care products,PCPs)4大类,其中检出浓度最高的达到了μg·L~(-1)量级,在长期的污染下有可能对水生生物产生内分泌干扰效应或繁殖毒性,进而影响到整个水生生物种群的繁衍变化。因此,有必要根据我国地表水中PPCPs的污染水平,筛查出具有潜在生态风险的PPCPs。由于目前缺乏针对PPCPs类污染物的筛选体系,以国内外优先控制污染物筛选体系为基础,借鉴基于风险的欧洲兽药分级方法,利用风险指数(risk index,RI),筛选得出目前我国的地表水中有16种具有繁殖毒性的PPCPs的RI1,包括1种抗生素,5种激素类药物,3种其他药物和7种PCPs,其中乙炔雌二醇(ethinylestradiol,EE2)的RI最高(115 730),其次是壬基酚(nonylphenol,NP)(1 796)、邻苯二甲酸二丁酯(dibutyl phthalate,DBP)(255.31),对水生态环境有较高的风险的PPCPs需进一步进行较高层次的风险评价。  相似文献   

18.
针对水处理过程的消毒环节,着重探讨了医药品和个人护理用品(PPCPs)等新型环境污染物在氯化消毒过程中发生的转化行为,并分别针对酚类、醇类、醚类、酮类、胺类等典型结构化合物的氯化转化规律进行了归纳总结.同时,对消毒副产物所引起的潜在环境风险、健康效应进行了评述,为研发、优化该类污染物的处理工艺、提高风险管理水平提供科学依据.  相似文献   

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