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31.
Released Ag ions or/and Ag particles are believed to contribute to the cytotoxicity of Ag nanomaterials, and thus, the cytotoxicity and mechanism of Ag nanomaterials should be dynamic in water due to unfixed Ag particle:Ag+ ratios. Our recent research found that the cytotoxicity of PVP-Ag nanoparticles is attributable to Ag particles alone in 3 hr bioassays, and shifts to both Ag particles and released Ag+ in 48 hr bioassays. Herein, as a continued study, the cytotoxicity and accumulation of 50 and 100 nm Ag colloids in Escherichia coli were determined dynamically. The cytotoxicity and mechanisms of nano-Ag colloids are dynamic throughout exposure and are derived from both Ag ions and particles. Ag accumulation by E. coli is derived mainly from extracellular Ag particles during the initial 12 hr of exposure, and thereafter mainly from intracellular Ag ions. Fe3+ accelerates the oxidative dissolution of nano-Ag colloids, which results in decreasing amounts of Ag particles and particle-related toxicity. Na+ stabilizes nano-Ag colloids, thereby decreasing the bioavailability of Ag particles and particle-related toxicity. Humic acid (HA) binds Ag+ to form Ag+-HA, decreasing ion-related toxicity and binding to the E. coli surface, decreasing particle-related toxicity. HA in complex conditions showed a stronger relative contribution to toxicity and accumulation than Na+ or Fe3+. The results highlighted the cytotoxicity and mechanism of nano-Ag colloids are dynamic and affected by environmental factors, and therefore exposure duration and water chemistry should be seriously considered in environmental and health risk assessments.  相似文献   
32.
Changes in water quality from source water to finished water and tap water at two conventional drinking water treatment plants(DWTPs) were monitored.Beside the routine water quality testing,Caenorhabditis elegans-based toxicity assays and the fluorescence excitation–emission matrices technique were also applied.Both DWTPs supplied drinking water that met government standards.Under current test conditions,both the investigated finished water and tap water samples exhibited stronger lethal,genotoxic and reprotoxic potential than the relative source water sample,and the tap water sample was more lethal but tended to be less genotoxic than the corresponding finished water sample.Meanwhile,the nearly complete removal of tryptophan-like substances and newly generated tyrosine-like substances were observed after the treatment of drinking water,and humic-like substances were identified in the tap water.Based on these findings,toxic pollutants,including genotoxic/reproductive toxicants,are produced in the drinking water treatment and/or distribution processes.Moreover,further studies are needed to clarify the potentially important roles of tyrosine-like and humic-like substances in mediating drinking water toxicity and to identify the potential sources of these contaminants.Additionally,tryptophan-like fluorescence may be adopted as a useful parameter to monitor the treatment performance of DWTPs.Our observations provided insights into the importance of utilizing biotoxicity assays and fluorescence spectroscopy as tools to complement the routine evaluation of drinking water.  相似文献   
33.
In this work, a series of Cu-ZSM-5 catalysts with different SiO2/Al2O3 ratios (25, 50, 100 and 200) were synthesized and investigated in n-butylamine catalytic degradation. The n-butylamine can be completely catalytic degradation at 350°C over all Cu-ZSM-5 catalysts. Moreover, Cu-ZSM-5 (25) exhibited the highest selectivity to N2, exceeding 90% at 350°C. These samples were investigated in detail by several characterizations to illuminate the dependence of the catalytic performance on redox properties, Cu species, and acidity. The characterization results proved that the redox properties and chemisorption oxygen primarily affect n-butylamine conversion. N2 selectivity was impacted by the Brønsted acidity and the isolated Cu2+ species. Meanwhile, the surface acid sites over Cu-ZSM-5 catalysts could influence the formation of Cu species. Furthermore, in situ diffuse reflectance infrared Fourier transform spectra was adopted to explore the reaction mechanism. The Cu-ZSM-5 catalysts are the most prospective catalysts for nitrogen-containing volatile organic compounds removal, and the results in this study could provide new insights into catalysts design for VOC catalytic oxidation.  相似文献   
34.
Ground-level ozone (O3) has become a critical pollutant impeding air quality improvement in Yangtze River Delta region of China. In this study, we present O3 pollution characteristics based on one-year online measurements during 2016 at an urban site in Nanjing, Jiangsu Province. Then, the sensitivity of O3 to its precursors during 2 O3 pollution episodes in August was analyzed using a box model based on observation (OBM). The relative incremental reactivity (RIR) of hydrocarbons was larger than other precursors, suggesting that hydrocarbons played the dominant role in O3 formation. The RIR values for NOX ranged from –0.41%/% to 0.19%/%. The O3 sensitivity was also analyzed based on relationship of simulated O3 production rates with reductions of VOC and NOX derived from scenario analyses. Simulation results illustrate that O3 formation was between VOCs-limited and transition regime. Xylenes and light alkenes were found to be key species in O3 formation according to RIR values, and their sources were determined using the Positive Matrix Factorization (PMF) model. Paints and solvent use was the largest contributor to xylenes (54%), while petrochemical industry was the most important source to propene (82%). Discussions on VOCs and NOX reduction schemes suggest that the 5% O3 control goal can be achieved by reducing VOCs by 20%. To obtain 10% O3 control goal, VOCs need to be reduced by 30% with VOCs/NOX larger than 3:1.  相似文献   
35.
为研究大气边界层中上层大气颗粒物的数浓度谱分布特征及气团来源的影响,于2018年6月利用3080型SMPS粒径谱仪对武当山14.6~660 nm颗粒物数浓度谱进行观测,分析和探讨了其数浓度谱分布及日变化特征,并结合后向轨迹、潜在源贡献因子法(PSCF)与浓度权重轨迹分析法(CWT)探讨对武当山颗粒物数浓度影响较大的外源输送路径和贡献源区.结果表明:①武当山大气颗粒物主要以爱根模态为主,平均数浓度为2 500个/cm3,积聚模态、核膜态平均数浓度分别为2 265、359个/cm3,3种模态数浓度分别占总数浓度的48.79%、44.21%、7.01%.②在新粒子生成日,核膜态数浓度于10:00开始上升,11:00—17:00的核膜态数浓度相对较高,约2 000个/cm3.新粒子生成日ρ(SO2)与ρ(O3)的日变化趋势均与核模态数浓度较为相似,表明SO2和O3参与光化学反应后的产物(硫酸及有机物)有利于新粒子的生成与增长.新粒子生成日风速、温度均大于非新粒子生成日,但相对湿度较低.③在东部及局地气团影响下大气颗粒物主要以积聚模态为主,数浓度分别为2 311和2 596个/cm3;核模态、爱根模态数浓度在受西北气团影响时最大,数浓度分别为806和3 078个/cm3.④潜在源区分析表明,影响武当山积聚模态数浓度的主要源区为十堰市本地及襄阳市,二者贡献值在840个/cm3以上.研究显示,武当山颗粒物主要以爱根模态为主,颗粒物数浓度日变化主要受大气边界层发展及山谷风的影响,较高的ρ(SO2)与ρ(O3)以及高温、低湿及较大的风速均有利于新粒子的生成,周边城市的区域性传输对武当山颗粒物的影响较大.   相似文献   
36.
为揭示河口区陆基养虾塘从养殖期到非养殖期一年间的CO2通量变化,以福建省闽江河口鳝鱼滩陆基养虾塘为研究对象,于2016年5月-2017年3月采用悬浮箱/静态箱-气相色谱法对养虾塘养殖期水-大气界面和非养殖期沉积物-大气界面白天CO2垂直通量进行原位观测.结果表明:①养虾塘在整个研究期间CO2通量变化范围为-62.87~162.81 mg/(m2·h),平均值为(42.66±18.12)mg/(m2·h),总体上表现为大气CO2的释放源,且呈非养殖期CO2通量平均值[(78.51±16.61)mg/(m2·h)]显著高于养殖期[(17.98±18.26)mg/(m2·h)]的特征.②养殖期间,养虾塘CO2通量呈"排放-吸收"交替变化的特征,而非养殖期养虾塘一直是大气CO2的净排放源.③养虾塘养殖期CO2通量时间变化特征主要受到ρ(DOC)(DOC为总溶解有机碳)、ρ(SO42-)、ρ(Cl-)、盐度、pH、ρ(Chla)(Chla为叶绿素a)的影响,其中,pH和ρ(SO42-)是其主要影响因子,而ρ(TDN)(TDN为总溶解氮)、ρ(TDP)(TDP为总溶解磷)、ρ(SO42-)对非养殖期CO2通量时间变化影响较大.研究显示,滨海陆基养殖塘是大气CO2的重要来源,其排放通量多低于河流、水库等水生生态系统,但高于湖泊生态系统;养殖塘CO2通量受人为影响明显,其较高的变异性与养殖生物、饲料投放以及浮游藻类有关.   相似文献   
37.
达里诺尔湖水体DOM荧光特征及其来源解析   总被引:1,自引:0,他引:1       下载免费PDF全文
孙伟  胡泓  赵茜  王璐  夏瑞  王晓  卜利胜  薛婕 《环境科学研究》2020,33(9):2084-2093
达里诺尔湖(简称“达里湖”)是内蒙古自治区高原地区重要的生态屏障,探究达里湖水质状况及污染来源,对加强流域水环境治理、改善水环境质量具有十分重要的意义.于2018年9月及2019年6月对湖水进行采样,并通过三维荧光光谱结合PARAFAC(平行因子分析)模型,探究达里湖水体DOM(溶解性有机质)来源及其与水质的关系.结果表明:①达里湖水体中pH较高,ρ(DOC)(DOC为溶解性有机碳)、ρ(NH4+-N)、ρ(TP)相对较高,均超过GB 3838—2002《地表水环境质量标准》Ⅴ类水质标准限值.②水体中DOM含4种荧光组分.夏季水体DOM主要分布于河流入湖口附近,其中,类腐殖质荧光组分(紫外区类富里酸和可见区类富里酸)占总组分的62.93%,类蛋白类荧光组分(类色氨酸和类酪氨酸)占总组分的36.07%;秋季水体DOM主要分布于东南侧,其中,类腐殖质荧光组分占总组分的40.52%,类蛋白类荧光组分占总组分的59.48%.③达里湖采样点荧光参数表明,达里湖DOM自生源特征较强,腐殖化程度较低.类腐殖质荧光组分与ρ(DOC)、ρ(Chla)均呈正相关,类色氨酸荧光组分与pH呈正相关,类络氨酸与ρ(DTN)、ρ(NH4+-N)、ρ(DTP)均呈正相关.研究显示,达里湖DOM具有陆源与生物源双重特性,DOM的形成与微生物、细菌、浮游生物的生命活动密切相关.   相似文献   
38.
严春丽  赵明  李泽坤  李金  段云松 《环境工程》2020,38(12):59-63,5
基于2016—2018年罗时江、弥苴河、永安江及洱海北部湖区监测数据分析,探讨洱海北部入湖河流污染变化特征及对北部湖区的影响。结果表明:1)"北三江"监测断面总磷、COD、氨氮浓度整体稳定在GB 3838—2002《地表水环境质量标准》Ⅱ—Ⅲ类标准限值内,年内污染物浓度变化表现出典型的农业面源污染特征,且受流域内产业模式等的综合影响;2)研究期间,河流首要污染物为TN,旱季次要污染物为COD,雨季为TP。雨季入湖负荷高于旱季,弥苴河污染负荷大于罗时江、永安江。"北三江"入湖TN和TP污染负荷分别占洱海允许负荷的50.1%和59.7%;3)入湖河流的磷元素输入是洱海北部湖区磷污染的重要来源。北部湖区污染物浓度对氮、磷入湖污染负荷相关性次月强于当月,响应存在延迟。筛选环境友好型种植模式,控制"北三江"氮磷入湖负荷,有利于保护洱海水环境。  相似文献   
39.
周蓓  关玥  赵亚芳  孔海南  林燕 《环境工程》2020,38(8):244-248
应用1套改良型水质综合指数法对3种不同类型的饮用水水质进行评价。将选取的26项检测指标按照卫生学意义分为5大类,并对各分类指标赋权。选用内梅罗法和最差因子判别法与五色等级分级法结合对2017年4—8月的3种类型饮用水进行水质评价。除7月和8月的管网水水质为2级(水质综合指数>0.5,蓝色)以外,其余月份的出水水质均达到1级(绿色)评价标准。不同类型饮用水中对水质综合指数影响最大的水质分类指标均是有机污染指标。2种不同类型的净水机出水水质均优于管网末梢水,但需注意个别指标的污染。  相似文献   
40.
水量、泥沙和污染物交换作为河流与湖泊之间的关键过程,对湖泊生态环境演变具有复杂而深远的影响.以长江中游典型通江湖泊洞庭湖为研究对象,着眼于“江湖”“河湖”“人湖”三重作用关系变化,从水文情势、水质、富营养化3个层面剖析了近30年洞庭湖水环境演变态势及主控因素.结果表明:①“江湖”关系变化影响了洞庭湖水沙交换及其年内分配,是湖泊枯水期提前和延长、水沙关系突变等现象的主控因素;“河湖”“人湖”关系变化协同加剧了该现象.②“河湖”关系的失衡和“河湖”统筹管理措施缺位,造成入湖河流长期输送大量营养物质,是湖体氮磷污染较重的根源;“江湖”“人湖”关系变化协同影响着营养盐分布格局,但影响范围及程度有限.③在“江湖”“河湖”作用关系复合影响下,藻类生长条件更为有利,增加了洞庭湖富营养化及水华风险.为保障洞庭湖水环境安全,建议:针对“江湖”作用主导的低枯水位问题,以水资源调控为核心,推进长江与流域上游水库联合生态调度,保障湖泊生态流量;针对“河湖”作用主导的水质恶化问题,以水污染防治为核心,强化流域污染控制,统筹“河湖”一体化监测管理模式,保障湖泊水环境质量;对于“人湖”作用主导的生态破坏问题,以生态空间管控为核心,划定并坚守生态红线,保障生态空间.   相似文献   
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