共查询到20条相似文献,搜索用时 12 毫秒
1.
正Introduction Natural organic matter(NOM)present in source water has significant impact on water treatment processes and on the quality of drinking water.NOM is a complex mixture of diverse groups of organic compounds,humic and fulvic acids,proteins,peptides,carbohydrates,and heterogeneous materials 相似文献
2.
Dissolved organic matter(DOM) has been identified as precursor for disinfection by-products(DBPs) formation during chlorination. Recently,it has been demonstrated that the characteristics of DOM influence the DBPs formation mechanism. A study was,therefore,initiated to investigate the effects of DOM fractions on DBPs formation mechanism. In the chlorination process,organic acids are dominant precursors of total thihalomethanes(TTHM) because of the νC-O and unsaturated structures. Furthermore,the TTHM format... 相似文献
3.
Da Sheng Lingjun Bu Shumin Zhu Yangtao Wu Jue Wang Nan Li Shiqing Zhou 《环境科学学报(英文版)》2022,34(7):21-27
Pre-oxidation has been reported to be an effective way to remove algal cells in water, but the released algal organic matter (AOM) could be oxidized and lead to the increment in disinfection by-product (DBP) formation. The relationship between pre-oxidation and AOM-derived DBP formation needs to be approached more precisely. This study compared the impact of four pre-oxidants, ozone (O3), chlorine dioxide (ClO2), potassium permanganate (KMnO4) and sodium hypochlorite (NaClO), on the formation of nitrogenous (N-) and carbonaceous (C-) DBPs in AOM chlorination. The characterization (fluorescent properties, molecular weight distribution and amino acids concentration) on AOM samples showed that the characterization properties variations after pre-oxidation were highly dependent on the oxidizing ability of oxidants. The disinfection experiments showed that O3 increased DBP formation most significantly, which was consistent with the result of characterization properties variations. Then canonical correspondent analysis (CCA) and Pearson's correlation analysis were conducted based on the characterization data and DBP formation. CCA indicated that C-DBPs formation was highly dependent on fluorescent data. The formation of haloacetic acids (HAAs) had a positive correlation with aromatic protein-like component while trichloromethane (TCM) had a positive correlation with fulvic acid-like component. Pearson's correlation analysis showed that low molecular weight fractions were favorable to form N-DBPs. Therefore, characterization data could provide the advantages in the control of DBP formation, which further revealed that KMnO4 and ClO2 were better options for removing algal cells as well as limiting DBP formation. 相似文献
4.
This work investigated the formation of carbonaceous and nitrogenous disinfection by-products (C-DBPs, N-DBPs) upon chlorination of water samples collected from a surface water and a ground water treatment plant (SWTP and GWTP) where the conventional treatment processes, i.e., coagulation, sedimentation, and filtration were employed. Twenty DBPs, including four trihalomethanes, nine haloacetic acids, seven N-DBPs (dichloroacetamide, trichloroacetamide, dichloroacetonitrile, trichloroacetonitrile, bromochloroacetonitrile, dibromoacetonitrile and trichloronitromethane), and eight volatile chlorinated compounds (dichloromethane (DCM), 1,2-dichloroethane, tetrachloroethylene, chlorobenzene, 1,2-dichlorobenzene, 1,4-dichlorobenzene, 1,2,3-trichlorobenzene and 1,2,4-trichlorobenzene) were detected in the two WTPs. The concentrations of these contaminants were all below their corresponding maximum contamination levels (MCLs) regulated by the Standards for Drinking Water Quality of China (GB5749-2006) except for DCM (17.1 μg/L detected vs. 20 μg/L MCL). The SWTP had much higher concentrations of DBPs detected in the treated water as well as the DBP formation potentials tested in the filtered water than the GWTP, probably because more precursors (e.g., dissolved organic carbon, dissolved organic nitrogen) were present in the water source of the SWTP. 相似文献
5.
6.
The migration and transformation of dissolved organic matter during the freezing processes of water 总被引:1,自引:0,他引:1
This study investigated the partitioning behavior of dissolved organic matter (DOM) in liquid and ice phases, as well as the changes in the optical properties and chlorine reactivity of DOM during the freezing processes of water. DOM was rejected from the ice phase and accumulated in the remaining liquid phase during water freezing. Moreover, the decrease in freezing temperature, as well as the increase in dissolved organic carbon (DOC) concentration of feed water, caused an increase in DOM captured in the ice phase. The ultraviolet-absorbing compounds, trihalomethane precursors, as well as fulvic acid- and humic acid-like fluorescent materials, were more liable to be to be rejected from the ice phase and were more easily retained in the unfrozen liquid phase during water freezing, as compared with organics (on average) that comprise DOC. In addition, it was also found a higher accumulation of these organics in the unfrozen liquid phase during water freezing at higher temperature. The freeze/thaw processes altered the quantity, optical properties, and chlorine reactivity of DOM. The decrease in ultraviolet light at 254 nm as well as the production of aromatic protein- and soluble microbial byproduct-like fluorescent materials in DOM due to freeze/thaw were consistently observed. On the other hand, the changes in DOC, trihalomethane formation potential, and fulvic acid- and humic acid-like fluorescence caused by freeze/thaw varied significantly between samples. 相似文献
7.
Tian-Yang Zhang Yong-Shan Lu Zhen-Ning Luo Wen-Jun Sun Bin Xu Chen-Yan Hu Yu-Lin Tang Zheng-Yu Dong Xiao-Meng Ren 《环境科学学报(英文版)》2022,34(7):141-150
UV/peroxymonosulfate (UV/PMS) advanced oxidation process has attracted significant attention for removal of micropollutants in water. However, during practical water treatment applications, the PMS treatment must be performed before the UV treatment to achieve full contact. In this study, sulfamethoxazole (SMX) was selected as the target micropollutant. Four different operational approaches, including UV alone, PMS alone, simultaneous UV/PMS and sequential PMS-UV, were compared for their differences in SMX removal and disinfection by-product (DBP) formation potentials during chlorine-driven disinfection. Among the four approaches, UV/PMS and PMS-UV achieved over 90% removal efficiencies for SMX without substantial differences. For raw water, the trichloronitromethane (TCNM) formation potential after treatment with PMS-UV was lower than that after UV/PMS treatment. The time interval over which the PMS-UV process was conducted had little effect on the final removal efficiency for SMX. However, a brief (5 min) pre-PMS treatment significantly reduced the TCNM formation potential and the genotoxicity from DBPs. The formation risk for TCNM during chlorination increased markedly with increasing PMS dosages, and the appropriate dosage under these experimental conditions was suggested to be 0.5–1.0 mmol/L. Under alkaline conditions, PMS-UV treatment can enhance SMX degradation as well as dramatically reduced the formation potentials for haloketones, haloacetonitriles and halonitromethanes. This study suggests that proper optimization of UV/PMS processes can remove SMX and reduce its DBP formation. 相似文献
8.
Clara H. Jeong Edward J. Machek Morteza Shakeri Stephen E. Duirk Thomas A. Ternes Susan D. Richardson Elizabeth D. Wagner Michael J. Plewa 《环境科学学报(英文版)》2017,29(8):173-182
The presence of iodinated X-ray contrast media (ICM) in source waters is of high concern to public health because of their potential to generate highly toxic disinfection by-products (DBPs). The objective of this study was to determine the impact of ICM in source waters and the type of disinfectant on the overall toxicity of DBP mixtures and to determine which ICM and reaction conditions give rise to toxic by-products. Source waters collected from Akron, OH were treated with five different ICMs, including iopamidol, iopromide, iohexol, diatrizoate and iomeprol, with or without chlorine or chloramine disinfection. The reaction product mixtures were concentrated with XAD resins and the mammalian cell cytotoxicity and genotoxicity of the reaction mixture concentrates was measured. Water containing iopamidol generated an enhanced level of mammalian cell cytotoxicity and genotoxicity after disinfection. While chlorine disinfection with iopamidol resulted in the highest cytotoxicity overall, the relative iopamidol-mediated increase in toxicity was greater when chloramine was used as the disinfectant compared with chlorine. Four other ICMs (iopromide, iohexol, diatrizoate, and iomeprol) expressed some cytotoxicity over the control without any disinfection, and induced higher cytotoxicity when chlorinated. Only iohexol enhanced genotoxicity compared to the chlorinated source water. 相似文献
9.
10.
Carbon source is a critical constraint on nutrient removal in domestic wastewater treatment. However, the functions of particulate organic matter (POM) and some organics with high molecular weight (HMW) are overlooked in the conventional process, as they cannot be directly assimilated into cells during microbial metabolism. This further aggravates the problem of carbon source shortage and thus affects the effluent quality. Therefore, to better characterize organic matter (OM) based MW distribution, microfiltration/ultrafiltration/nanofiltration (MF/UF/NF) membranes were used in parallel to fractionate OM, which obtained seven fractions. Hydrolysis acidification (HA) was adopted to manipulate the MW distribution of dissolved organic matter (DOM) and further explore the correlation between molecular size and biodegradability. Results showed that HA pretreatment of wastewater not only promoted transformation from POM to DOM, but also boosted biodegradability. After 8 hr of HA, the concentration of dissolved organic carbon (DOC) increased by 65%, from the initial value of 20.25 to 33.48 mg/L, and the biodegradability index (BOD5 (biochemical oxygen demand)/SCOD (soluble chemical oxygen demand)) increased from 0.52 to 0.74. Using MW distribution analysis and composition optimization, a new understanding on the characteristics of organics in wastewater was obtained, which is of importance to solving low C/N wastewater treatment in engineering practice. 相似文献
11.
以锦州市W污水处理厂为研究对象,利用三维荧光光谱分析技术和荧光区域积分(FRI)方法考察了城市污水处理过程中溶解性有机物及荧光物质的去除状况.利用XAD树脂将DOM分为5个部分:疏水性有机酸(HPO-A)、疏水性中性有机物(HPO-N)、过渡亲水性有机酸(TPIA)、过渡亲水性中性有机物(TPI-N)和亲水性有机物(HPI).结果表明,HPO-A和HPI是该污水处理厂进水中的主要DOM组分,并且DOM中的荧光物质主要为类芳香族蛋白质荧光物质和类富里酸荧光物质.在该污水处理厂内,生物降解作用是TPI-A和HPI的主要去除机制,HPO-N和TPI-N主要是由深度处理工艺(絮凝-沉淀-过滤)去除的,生物处理工艺和深度处理工艺对HPO-A的去除能力接近,而生物处理工艺和深度处理工艺对TPI-N的去除效果均较差.生物处理工艺对HPO-A、TPI-A和HPI中的荧光物质有较强的去除能力,而对HPO-N和TPI-N中荧光物质的去除效果较差.深度处理工艺能够有效去除HPO-A和HPO-N中的荧光物质,而对TPI-A、TPI-N和HPI中的荧光物质无明显去除作用. 相似文献
12.
Coagulation–ultrafiltration(C–UF) is widely used for surface water treatment. With the removal of pollutants, the characteristics of organic matter change and affect the final treatment efficiency and the development of membrane fouling. In this study, we built a dynamic C–UF set-up to carry out the treatment of micro-polluted surface water, to investigate the characteristics of dissolved organic matter from different units. The influences of poly aluminum chloride and poly dimethyldiallylammonium chloride(PDMDAAC) on removal efficiency and membrane fouling were also investigated. Results showed that the dosage of PDMDAAC evidently increased the UV254 and dissolved organic carbon removal efficiencies,and thereby alleviated membrane fouling in the C–UF process. Most hydrophobic bases(HoB)and hydrophobic neutral fractions could be removed by coagulation. Similarly, UF was good at removing HoB compared to hydrophilic substances(HiS) and hydrophobic acid(HoA)fractions. HiS and HoA fractions with low molecule weight accumulated on the surface of the membrane, causing the increase of transmembrane pressure(TMP). Membrane fouling was mainly caused by a removable cake layer, and mechanical cleaning was an efficient way to decrease the TMP. 相似文献
13.
It is very important to identify the dominant precursors for N-nitrosamine formation from bulk organic matter, to enhance the understanding of N-nitrosamine formation pathways in water treatment plants and allow the development of practical treatment technologies. In this study, dissolved organic matter (DOM) from two source waters was fractionated with XAD resins and ultra- filtration membranes. The N-nitrosamine formation potential (FP) (ng of N-nitrosamines formed per mg of dissolved organic carbon (DOC)) from raw water and each fraction were measured and correlated with the fluorescence excitation-emission matrix (EEM), molecular weight (MW) and other assays. The results showed that the hydrophilic fraction had N-nitrosamine FP 1.3 to 3.5 times higher than the hydrophobic fraction from both source waters. The DOM fraction with low MW was the dominant fraction in these two source waters and contributed more precursors for N-nitrosamine formation than the larger MW fraction. The EEM spectra indicated there were notable amounts of soluble microbial products (SMPs) and aromatic proteins in the two studied rivers, which probably originated from wastewater discharge. The SMPs tended to be more closely correlated with N-nitrosodimethylamine formation potential than the other DOM components. Higher N-nitrosamine FP were also related to fractions with lower DOC/DON ratios and lower SUVA 254 values. 相似文献
14.
冬季不同污水处理工艺对溶解性有机物的去除 总被引:1,自引:0,他引:1
以东北地区4个城市污水处理厂为研究对象,考察冬季不同污水处理工艺对溶解性有机物(DOM)组分的去除效果,以及对DOM组分的光谱学特性和卤代活性的影响.利用XAD树脂将DOM分为5个部分:疏水性有机酸(HPO-A)、疏水性中性有机物(HPO-N)、过渡亲水性有机酸(TPI-A)、过渡亲水性中性有机物(TPI-N)和亲水性有机物(HPI).结果表明,A/O法、曝气生物滤池、浮动填料法和A2/O法对DOM都具有较高的去除能力,其中曝气生物滤池对DOM的处理效果最好.经4种污水处理工艺处理后,5种组分的芳香性和三卤甲烷生成活性(STHMFP)均升高.A2/O法对HPO-A和TPI-A的芳香性增强程度最高,而曝气生物滤池对HPO-N,TPI-N和HPI的芳香性增强程度最高.浮动填料法对HPO-A,TPI-A和HPI的STHMFP升高最显著,A2/O法对HPO-N的STHMFP增加最显著,曝气生物滤池对TPI-N的STHMFP升高最显著.4种污水处理工艺对HPI中荧光物质的去除率高于非荧光物质.而对于其他4种DOM组分来说,不同的污水处理工艺对不同荧光峰的改变不相同. 相似文献
15.
城市污水二级出水有机物分子量分布和亲疏水特性对纳滤膜污染的影响 总被引:8,自引:1,他引:7
分别采用分子量分级膜和XAD-8树脂,研究了污水厂二级出水中有机物分子量分布特征及不同分子量分布区间亲疏水有机物的相对含量,考察了分子量分布及亲疏水特性对纳滤膜透水性能的影响.结果表明,二级出水有机物中,小分子亲水性有机物含量最高,小于2k的有机物占总有机物含量的45.61%,其中亲水性物质占28.07%,疏水性物质占17.54%;不同特征的原水分别经纳滤膜过滤,分子量分布对膜污染影响较大,分子量小于30k时,分子量区间越小,比通量衰减越快,分子量大于30k时,分子量区间越大,比通量衰减越快,且分子量较小的有机物通量衰减程度大于分子量较大有机物;在分子量分布相同区间内,亲水性有机物的比通量衰减较慢,说明相同分子量时,膜对亲水性物质的截留率较低,而疏水性物质是引起膜通量衰减的主要原因. 相似文献
16.
底泥、土壤均是水体有机物的重要来源,但目前相关消毒副产物(DBPs)形成方面的研究偏少.本研究以长三角重要水源地太湖、钱塘江取水口的底泥和周边土壤的浸出液为研究对象,探索氯、臭氧+氯、氯胺、臭氧+氯胺4种消毒方式下,三卤甲烷(THMs)、卤代酮(HKs)、卤乙腈(HANs)、卤代硝基甲烷(HNMs)的形成情况.结果表明,太湖、钱塘江取水口的底泥、周边土壤有机物的芳香度均很低(SUVA254(即比紫外吸光值)2),与腐殖质(Sigma)相比,底泥、土壤有机物不是氯消毒中THMs的重要前驱物,但却是HANs特别是HNMs的重要前驱物.相比氯消毒,氯胺消毒能大幅降低土壤、底泥有机物THMs、HKs、HANs、HNMs的生成量,而且也可抑制含溴DBPs的形成.臭氧预处理大幅提高了氯、氯胺消毒中HKs、HNMs的产量,但对THMs、HANs则不一定.太湖、钱塘江的土壤、底泥存在一定的溴污染,但不管是哪种消毒方式,均是HNMs的溴嵌入因子最大. 相似文献
17.
Ying Zhu Lu Chen Hong Xiao Fei Shen Shihuai Deng Shirong Zhang Jinsong He Chun Song Xie Wang Jianhua Zhang Li Gong Chun Hu 《环境科学学报(英文版)》2020,32(2):273-282
The effects of disinfection efficiency on microbial communities and the corrosion of cast iron pipes in drinking water distribution systems (DWDSs) were studied. Two annular reactors (ARs) that simulated actual running conditions with UV/Cl2 disinfection and chlorination alone were used. High chlorine consumption and corrosion rate were found in the AR with UV/Cl2. According to functional genes and pyrosequencing tests, a high percentage of iron recycling bacteria was detected within the biofilm of the AR with Cl2 at early running stage, whereas siderophore-producing bacteria were dominant in the biofilm of the AR with UV/Cl2. At the early running stage, the sequential use of UV light and an initial high chlorine dosage suppressed the biomass and iron-recycling bacteria in both bulk water and biofilms, thereby forming less protective scales against further corrosion, which enhanced chlorine consumption. Non-metric multidimensional scaling analysis showed that the bacterial communities in the ARs shaped from within rather than being imported by influents. These results indicate that the initial high disinfection efficiency within the distribution system had not contributed to the accumulation of iron-recycling bacteria at the early running stages. This study offer certain implications for controlling corrosion and water quality in DWDSs. 相似文献
18.
Chlorine dioxide (ClO2) disinfection usually does not produce halogenated disinfection by-products, but the formation of the inorganic by-product chlorite (ClO2–) is a serious consideration. In this study, the ClO2– formation rule in the ClO2 disinfection of drinking water was investigated in the presence of three representative reductive inorganics and four natural organic matters (NOMs), respectively. Fe2+ and S2– mainly reduced ClO2 to ClO2– at low concentrations. When ClO2 was consumed, the ClO2– would be further reduced by Fe2+ and S2–, leading to the decrease of ClO2–. The reaction efficiency of Mn2+ with ClO2 was lower than that of Fe2+ and S2–. It might be the case that MnO2 generated by the reaction between Mn2+ and ClO2 had adsorption and catalytic oxidation on Mn2+. However, Mn2+ would not reduce ClO2–. Among the four NOMs, humic acid and fulvic acid reacted with ClO2 actively, followed by bovine serum albumin, while sodium alginate had almost no reaction with ClO2. The maximum ClO2– yields of reductive inorganics (70%) was higher than that of NOM (around 60%). The lower the concentration of reductive substances, the more ClO2– could be produced by per unit concentration of reductive substances. The results of the actual water samples showed that both reductive inorganics and NOM played an important role in the formation of ClO2– in disinfection. 相似文献
19.
以上海市黄浦江和青草沙长江原水为对象,研究了两大水源水中溶解性有机氮(DON)的含量变化、分子组成特征及其在常规净水工艺中的去除效果,并对DON与常规水处理指标间的相关性进行了分析.结果表明:两种原水以DOC、DON和UV254表征的有机物含量均以小分子量(<5kDa)和亲水性有机物为主;微污染黄浦江原水中同时存在外源性及内源性污染,而青草沙长江原水中内源性污染占主导地位;饮用水常规净水处理工艺对黄浦江原水中DON的去除率为40%,优于长江原水DON的去除率16.7%;黄浦江和长江原水DON浓度与DOC和UV254相关性良好,其相关系数分别为0.59,0.52和0.74,0.51;鉴于常规处理对DON去除效果有限,而DON是导致强三致特性含氮消毒副产物(N-DBPs)的总前体物,因此水厂应通过强化常规、深度处理等手段改善DON在净水工艺中的去除效果. 相似文献
20.
Distribution and spectral characteristics of chromophoric dissolved organic matter in a coastal bay in northern China 总被引:1,自引:0,他引:1
Guiju Li Jing Liu Yulan M Ruihua Zhao Suzheng Hu Yijie Li Hao Wei Huixiang Xie 《环境科学学报(英文版)》2014,26(8):1585-1596
The absorption spectra of chromophoric dissolved organic matter(CDOM),along with general physical,chemical and biological variables,were determined in the Bohai Bay,China,in the springs of 2011 and 2012. The absorption coefficient of CDOM at 350 nm(a350) in surface water ranged from 1.00 to 1.83 m-1(mean: 1.35 m-1) in May 2011 and from 0.78 to 1.92 m-1(mean:1.19 m-1) in April 2012. Little surface-bottom difference was observed due to strong vertical mixing. The a350 was weakly anti-correlated to salinity but positively correlated to chlorophyll a(Chl-a) concentration. A shoulder over 260–290 nm,suggestive of biogenic molecules,superimposed the overall pattern of exponentially decreasing CDOM absorption with wavelength. The wavelength distribution of the absorption spectral slope manifested a pronounced peak at ca. 300 nm characteristic of algal-derived CDOM. All a250/a365 ratios exceeded 6,corresponding to CDOM molecular weights(Mw) of less than 1 kDa. Spectroscopically,CDOM in the Bohai Bay differed substantively from that in the Haihe River,the bay's dominant source of land runoff; photobleaching of the riverine CDOM enlarged the difference.Results point to marine biological production being the principal source of CDOM in the Bohai Bay during the sampling seasons. Relatively low runoff,fast dilution,and selective photodegradation are postulated to be among the overarching elements responsible for the lack of terrigenous CDOM signature in the bay water. 相似文献