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Yufeng Liao Mengmeng Tang Mengyuan Li Peng Shi Aimin Li Yangyang Zhang Yang Pan 《Frontiers of Environmental Science & Engineering》2023,17(10):125
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Chengkun Wang Xiaojian Zhang Chao Chen Jun Wang 《Frontiers of Environmental Science & Engineering》2013,7(2):151-157
The formation of cancinogenic nitrosamines, esp. N-nitrosodimethylamine (NDMA) in water and wastewater treatment plants has drawn much attention in recent years. Dissolved organic matter from the transported Luan River water as water source of Tianjin was fractionated with different XAD resins and a series of ultra-filtration membranes with molecular weight (MW) cut-offs of 5k Da, 3k Da, and 1k Da, respectively. The NDMA yields from the raw water and each fraction were measured to investigate their role in NDMAyield. Results indicated that the hydrophilic fraction had a higher NDMA yield than those of hydrophobic fraction and transphilic fraction. The fraction with MW below 1k Da had a higher NDMAyield than that with larger MW. NDMA formation increased as the dissolved organic carbon (DOC) to dissolved organic nitrogen (DON) ratio decreased, which indicated that DON might serve as the real important precursor for NDMA. The correlation between NDMA yield and specific ultraviolet absorbance at 254 nm (SUVA254) suggested that the latter might not represent the specific precursors for NDMA in the water. Besides the water quality, the influences of pH, disinfectant dosage, and disinfection contact time on the formation of NDMA were also examined. These results will help water treatment plants establish measures to control this harmful disinfection by-product. 相似文献
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Jinhui Liang Peng Gao Benhang Li Longfei Kang Li Feng Qi Han Yongze Liu Liqiu Zhang 《Frontiers of Environmental Science & Engineering》2022,16(12):150
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黄浦江原水中各类有机物在铝盐混凝过程中的去除效果 总被引:1,自引:0,他引:1
通过XAD-8/XAD-4吸附树脂联用技术将黄浦江微污染原水中溶解性有机物分为疏水酸、非酸疏水物质、弱疏水物质及亲水物质4类有机物,研究了铝盐混凝工艺对黄浦江水中4类有机物的去除效果.硫酸铝在最佳混凝条件下,即投加量为8 mg·l~(-1)(以Al计),pH=5.5时,水中的DOC和UV_(254)的去除率分别达到23%和32%.有机物的亲疏水性对混凝工艺有较大影响,混凝法倾向于优先去除水中疏水性有机物,而疏水性有机物的酸碱性对混凝工艺没有明显影响,酸性和非酸类疏水物质均能破混凝工艺所去除.疏水酸是水中最主要的三氯甲烷类消毒副产物的前体物质,混凝工艺对于三氯甲烷类消毒副产物有良好的控制作用,总体减少了 39%的生成量.而不同类的有机物之间,混凝工艺对消毒副产物控制效果不同,其中对疏水酸的控制三氯甲烷消毒副产物的效果最好,减少了63%的生成量,亲水物质的控制效果最差,三氯甲烷生成量仪减少了3%.疏水酸表现出比亲水物质更强的生物毒性,混凝工艺能明显降低原水的毒性. 相似文献
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Jianbing WANG Guoqing WANG Chunli YANG Shaoxia YANG Qing HUANG 《Frontiers of Environmental Science & Engineering》2015,9(4):615
This research investigates the performances of RuO2/ZrO2-CeO2 in catalytic ozonation for water treatment. The results show that RuO2/ZrO2-CeO2 was active for the catalytic ozonation of oxalic acid and possessed higher stability than RuO2/Al2O3 and Ru/AC. In the catalytic ozonation of dimethyl phthalate (DMP), RuO2/ZrO2-CeO2 did not enhance the DMP degradation rate but significantly improved the total organic carbon (TOC) removal rate. The TOC removal in catalytic ozonation was 56% more than that in noncatalytic ozonation. However this does not mean the catalyst was very active because the contribution of catalysis to the overall TOC removal was only 30%. The adsorption of the intermediates on RuO2/ZrO2-CeO2 played an important role on the overall TOC removal while the adsorption of DMP on it was negligible. This adsorption difference was due to their different ozonation rates. In the catalytic ozonation of disinfection byproduct precursors with RuO2/ZrO2-CeO2, the reductions of the haloacetic acid and trihalomethane formation potentials (HAAFPs and THMFPs) for the natural water samples were 38%–57% and 50%–64%, respectively. The catalyst significantly promoted the reduction of HAAFPs but insignificantly improved the reduction of THMFPs as ozone reacts fast with the THMs precursors. These results illustrate the good promise of RuO2/ZrO2-CeO2 in catalytic ozonation for water treatment. 相似文献
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Qian-Yuan Wu Yi-Jun Yan Yao Lu Ye Du Zi-Fan Liang Hong-Ying Hu 《Frontiers of Environmental Science & Engineering》2020,14(2):25
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焦化废水中溶解性有机物组分的特征分析 总被引:3,自引:0,他引:3
焦化废水是典型的具有复杂有机质的工业废水,其复杂的有机构成制约了水处理的水质达标,且可能对排入水体构成危害.为了探明其溶解性有机物的组成,采用XAD-8大孔树脂将焦化废水中的溶解性有机物分为亲水性组分(HIS)、疏水酸性组分(HOA)、疏水碱性组分(HOB)和疏水中性组分(HON),分析了各组分的溶解性有机物(DOC)、紫外-可见光谱、色度,并采用GC/MS对各组分中有机物进行定性分析.结果表明,焦化废水中的有机物主要为HIS和HOA组分,其DOC含量分别占总DOC的44.3%和32.4%;焦化废水在200—250 nm和300—400 nm范围内有特征吸收峰,且吸收光强度顺序为HIS>HOA>HON>HOB;焦化废水的色度主要由HOA和HON构成,其在525 nm和436 nm处的吸光度分别占焦化废水吸光度的42.9%(HON)、42.1%(HON)和21.4%(HOA)、15.8%(HOA);焦化废水中亲水性物质主要是苯胺、苯酚、喹啉、异喹啉,疏水酸性物质中主要是各种甲基取代的酚类物质,疏水碱性物质主要是各种胺类和含氮杂环化合物,疏水中性物质主要是吲哚及其衍生物. 相似文献
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京密引水中天然有机物的形态 总被引:4,自引:0,他引:4
用改进的Leenheer分离方法,并引入最新的XAD-8,XAD-4树脂串联技术,将京密引水中有机物定量分离为悬浮和溶解态两大类。后者又进一步分离为憎水有机物、腐殖酸类,XAD-4酸和亲水中性有机物等形成。溶解态有机物含量约为3mgC/l,其中一半左右为腐殖酸类。XAD-4酸占溶解态有机15-20%,非极性憎水有机物所占比例很低。 相似文献
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Yang PAN Xiangru ZHANG Jianping ZHAI 《Frontiers of Environmental Science & Engineering》2015,9(1):121
When bromide/iodide is present in source water, hypobromous acid/hypoiodous acid will be formed with addition of chlorine, chloramine, or other disinfectants. Hypobromous acid/hypoiodous acid undergoes reactions with natural organic matter in source water to form numerous brominated/iodinated disinfection byproducts (DBPs). In this study, tap water samples were collected from eight cities in China. With the aid of electrospray ionization-triple quadrupole mass spectrometry by setting precursor ion scans of m/z 35, m/z 81, and m/z 126.9, whole pictures of polar chlorinated, brominated, and iodinated DBPs in the tap water samples were revealed for the first time. Numerous polar halogenated DBPs were detected, including haloacetic acids, newly identified halogenated phenols, and many new/unknown halogenated compounds. Total organic chlorine, total organic bromine, and total organic iodine were also measured to indicate the total levels of all chlorinated, brominated, and iodinated DBPs in the tap water samples. The total organic chlorine concentrations ranged from 26.8 to 194.0 μg·L–1 as Cl, with an average of 109.2 μg·L–1 as Cl; the total organic bromine concentrations ranged from below detection limit to 113.3 μg·L–1 as Br, with an average of 34.7 μg·L–1 as Br; the total organic iodine concentrations ranged from below detection limit to 16.4 μg·L–1 as I, with an average of 9.1 μg·L–1 as I; the total organic halogen concentrations ranged from 31.3 to 220.4 μg·L–1 as Cl, with an average of 127.2 μg·L–1 as Cl. 相似文献
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This research work was performed to evaluate ozonation and granular activated carbon adsorption processes from the view‐point of controlling the formation of disinfection by products (DBPs). Both the humic acid and raw water were first preozonated and then adsorbed on the activated carbon to assess the potency for removal of total organic carbon (TOC) and DBPs. The disinfection by‐product including THMs and HAAs, in principle, can be successfully removed through a use of the ozonation and granular activated carbon (GAC) adsorption processes. However, in practice dealing with the raw water, it is necessary to introduce the pilot‐plant to obtain the design and operation guidelines for the water treatment plant through the ICA (Instrumentation Control and Automation) program in our future research work. 相似文献
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Shuang XUE Qingliang ZHAO Liangliang WEI Xiujuan HUI Xiping MA Yingzi LIN 《Frontiers of Environmental Science & Engineering》2012,6(6):784-796
This work investigated the effect of granular activated carbon adsorption (GACA) on fluorescence characteristics of dissolved organic matter (DOM) in secondary effluent, by means of excitation–emission matrix (EEM) spectra, the fluorescence regional integration (FRI) method, synchronous spectra, the fluorescence index defined as the ratio of fluorescence emission intensity at wavelength 450 nm to that at 500 nm at excitation (λ ex)=370 nm, and the wavelength that corresponds to the position of the normalized emission band at its half intensity (λ 0.5). DOM in the secondary effluent from the North Wastewater Treatment Plant (Shenyang, China) was fractionated using XAD resins into 5 fractions: hydrophobic acid (HPO–A), hydrophobic neutral (HPO–N), transphilic acid (TPI–A), transphilic neutral (TPI–N) and hydrophilic fraction (HPI). Results showed that fluorescent materials in HPO–N and TPI–N were less readily removed than those in the other fractions by GACA. The relative content of fluorescent materials in HPO–A, TPI–A and HPI decreased whereas that in HPO–N and TPI–N increased as a consequence of GACA. Polycyclic aromatics in all DOM fractions were preferentially absorbed by GACA, in comparison with bulk DOM expressed as DOC. On the other hand, the adsorption of aromatic amino acids and humic acid-like fluorophores exhibiting fluorescence peaks in synchronous spectra by GACA seemed to be dependent on the acid/neutral properties of DOM fractions. All five fractions had decreased fluorescence indices as a result of GACA. GACA led to a decreased λ 0.5 value for HPO–A, increased λ 0.5 values for HPO–N, TPI–A and HPI, and a consistent λ 0.5 value for TPI–N. 相似文献
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Xiaoman Liu Chang Tian Yanxia Zhao Weiying Xu Dehua Dong Kaimin Shih Tao Yan Wen Song 《Frontiers of Environmental Science & Engineering》2022,16(8):110
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Chemical identification and genotoxicity analysis of petrochemical industrial wastewater 总被引:2,自引:0,他引:2
Jing ZHANG Shigong WANG Can WANG Hongying HU 《Frontiers of Environmental Science & Engineering》2012,6(3):350-359
The actual harmful effects of industrial wastewater can not be reflected by the conventional water quality index. Therefore, the change in dissolved organic matter and the genetic toxicity of petrochemical wastewater were observed in the current study by examining the wastewater treatment plant of a large petrochemical enterprise in Northwest China. Using XAD-8, MSC, and DA-7 resins, the wastewater was separated into six fractions, namely, hydrophobic acid (HOA), hydrophobic neutral (HOB), hydrophobic alkaline, hydrophilic acid, hydrophilic alkaline, and hydrophilic neutral. Umu-test was used to detect the genetic toxicity of the wastewater samples, and fluorescence spectra were also obtained to examine genetic toxic substances. The results show that wastewater treatment facilities can effectively reduce the concentration of organic matter in petrochemical wastewater (p<0.05). However, the mixing of aniline wastewater can increase the amount of organic carbon (p<0.05) and can overload facilities. This finding shows that the mixed collection and joint treatment of different types of petrochemical wastewater can affect the water quality of the effluent. Particularly, hydrophobic substances can be difficult to remove and account for a relatively large proportion of the effluent. The mixture of aniline wastewater can increase the genetic toxicity of the effluent (p<0.05), and biologic treatment can not effectively decrease the toxicity. Most of the genetic toxicology may exist in the HOA and HOB fractions. Fluorescence spectroscopy also confirms this result, and tryptophan-like substances may play an important role in genetic toxicity. 相似文献
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Chen CY Lu CJ 《Journal of environmental biology / Academy of Environmental Biology, India》2004,25(4):477-483
This study focuses on the differences in biodegradation of the natural organic matters (NOMs) of p-hydroxy-benzoic acid (PHBA) and 4-hydroxy-3-methoxy-benzoic acid (VA) with slow sand filter (SSF). The PHBA and VA were biologically transformed into another organic matter in the slow sand filtration (SSF) at the start-up period. The dissolved organic carbon (DOC) of PHBA and VA were stabilized at 2 mg/l after 5th day. The SUVA value of PHBA run decreased with higher sand depth and flow rate, and VA run's increased with higher sand depth, but smaller than PHBA run. Therefore, the PHBA promoted the DBPFP (formation potential of disinfection by products), the VA brought higher biodegradation and lower DBPFP. 相似文献
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岩溶山区不同土地利用方式对土壤活性有机碳动态的影响 总被引:8,自引:2,他引:8
对贵州茂兰自然保护区内三种典型土地利用方式(林地、草地和耕地)下土壤活性有机碳组分(土壤溶解有机碳和土壤微生物量碳)的月变化及其对环境因子的响应进行了研究,结果表明在不同的土地利用方式下上覆植被类型不同,其凋落物数量、质量及分解行为不同,有机质的输入量及质量也不相同,从而形成不同的土壤溶解有机碳含量差异,土壤有机碳的大小也存在较大差别。研究结果显示:从全年平均值来看,林地土壤溶解有机碳分别比草地和耕地高25%、48%;从3月到8月,三者均随气温的上升呈增加的趋势,林地和耕地在8月均达到最大值,而草地则在10月达到最大值;林地和草地土壤微生物量碳分别高于耕地81%和45%,林地和草地在10月达到最大值。不同的土地利用方式导致土壤活性有机碳的差异较大,这说明岩溶生态系统中土地利用方式对土壤碳库的大小有较大影响。不同土地利用方式下土壤活性有机碳对环境因子的响应也各不相同,这表明土壤活性碳受众多因素的制约而呈现出一种动态平衡关系,进一步的机理仍需要进行深入研究。 相似文献
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Yuqing Xu Zedong Lu Wenjun Sun Xiaohui Zhang 《Frontiers of Environmental Science & Engineering》2021,15(6):131
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Mengqing Ge Tao Lin Kemei Zhou Hong Chen Hang Xu Hui Tao Wei Chen 《Frontiers of Environmental Science & Engineering》2021,15(5):93
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Xiaoyan SHI Kebin HE Weiwei SONG Xingtong WANG Jihua TAN 《Frontiers of Environmental Science & Engineering》2012,6(4):463-469
The effects of a diesel oxidation catalytic (DOC) converter on diesel engine emissions were investigated on a diesel bench at various loads for two steady-state speeds using diesel fuel and B20. The DOC was very effective in hydrocarbon (HC) and CO oxidation. Approximately 90%–95% reduction in CO and 36%–70% reduction in HC were realized using the DOC. Special attention was focused on the effects of the DOC on elemental carbon (EC) and organic carbon (OC) fractions in fine particles (PM2.5) emitted from the diesel engine. The carbonaceous compositions of PM2.5 were analyzed by the method of thermal/optical reflectance (TOR). The results showed that total carbon (TC), OC and EC emissions for PM2.5 from diesel fuel were generally reduced by the DOC. For diesel fuel, TC emissions decreased 22%–32% after the DOC depending on operating modes. The decrease in TC was attributed to 35%–97% decrease in OC and 3%–65% decrease in EC emissions. At low load, a significant increase in the OC/EC ratio of PM2.5 was observed after the DOC. The effect of the DOC on the carbonaceous compositions in PM2.5 from B20 showed different trends compared to diesel fuel. At low load, a slight increase in EC emissions and a significant decrease in OC/EC ratio of PM2.5 after DOC were observed for B20. 相似文献