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101.
针对修复焦化厂高浓度多环芳烃污染土壤高成本的现实,采用以非食用性植物油、生物柴油、表面活性剂及其乳化合成的微乳液为淋洗剂,比较不同淋洗剂的淋洗效果。结果表明乳化合成的微乳液对焦化厂土壤中多环芳烃的总去除率高于单独使用表面活性剂为淋洗剂对土壤中多环芳烃的总去除率,说明生物柴油及植物油与表面活性剂乳化形成的微乳液对原污染土壤中的多环芳烃具有显著的增溶作用。1%TW-80和2.5%TW-80对土壤中多环芳烃总去除率分别为11%和14%;以2.5%TW-80为原料乳化合成的微乳液的淋洗去除率较以1%TW-80为原料乳化合成的微乳液高,总去除率分别为15%~30%和11%~18%;以生物柴油为原料乳化合成的微乳液的淋洗去除率较以植物油为原料乳化合成的微乳液高,分别为17%~30%和15%~23%,且对多环芳烃的去除率与其辛醇水分配系数(logKow)呈线性相关关系。  相似文献   
102.
This study investigated the photocatalytic degradation of acetaminophen (ACT) in synthetic titanium dioxide (TiO2) solution under a visible light (λ >440 nm). The TiO2 photocatalyst used in this study was synthesized via sol–gel method and doped with potassium aluminum sulfate (KAl(SO4)2) and sodium aluminate (NaAlO2). The influence of some parameters on the degradation of acetaminophen was examined, such as initial pH, photocatalyst dosage, and initial ACT concentration. The optimal operational conditions were also determined. Results showed that synthetic TiO2 catalysts presented mainly as anatase phase and no rutile phase was observed. The results of photocatalytic degradation showed that LED alone degraded negligible amount of ACT but with the presence of TiO2/KAl(SO4)2, 95 % removal of 0.10-mM acetaminophen in 540-min irradiation time was achieved. The synthetic TiO2/KAl(SO4)2 presented better photocatalytic degradation of acetaminophen than commercially available Degussa P-25. The weak crystallinity of synthesized TiO2/NaAlO2 photocatalyst showed low photocatalytic degradation than TiO2/KAl(SO4)2. The optimal operational conditions were obtained in pH 6.9 with a dose of 1.0 g/L TiO2/KAl(SO4)2 at 30 °C. Kinetic study illustrated that photocatalytic degradation of acetaminophen fits well in the pseudo-first order model. Competitive reactions from intermediates affected the degradation rate of ACT, and were more obvious as the initial ACT concentration increased.  相似文献   
103.
长三角地区大气污染治理取得一定成效,然而空气质量改善逐渐进入瓶颈期和攻坚期,大气污染治理战略需要从宏观层面系统谋划。本文系统分析了近10年来长三角区域经济、能源、产业、交通的发展状况和趋势,结合区域大气污染物浓度水平的演变,分析了大气污染与经济社会发展的耦合关系。结合当前区域空气污染的空间分布差异以及经济能源交通结构的内在差别,识别了大气污染的区内差异特征及关键制约因素。在此基础上,从能源结构和产业结构调整、交通结构优化、分区施策、深化治理等角度,为深化区域大气污染联防联控,持续改善大气污染问题提出了政策建议。  相似文献   
104.
Triclocarban (TCC) is an antibacterial agent found in pharmaceuticals and personal care products (PPCP). It is potentially bioaccumulative and an endocrine disruptor, being classified as a contaminant of emerging concern (CEC). In normal uses, approximately 96% of the used TCC can be washed down the drain going into the sewer system and eventually enter in the aquatic environment. UV photolysis can be used to photodegrade TCC and ecotoxicity assays could indicate the photodegradation efficiency, since the enormous structural diversity of photoproducts and their low concentrations do not always allow to identify and quantify them. In this work, the TCC was efficiently degraded by UVC direct photolysis and the ecotoxicity of the UV-treated mixtures was investigated. Bioassays indicates that Daphnia similis (48 h EC50 = 0.044 μM) was more sensitive to TCC than Pseudokirchneriella subcapitata (72 h IC50 = 1.01 μM). TCC and its photoproducts caused significant effects on Eisenia andrei biochemical responses (catalase and glutathione-S-transferase); 48 h was a critical exposure time, since GST reached the highest activity values. UVC reduced the TCC toxic effect after 120 min. Furthermore, TCC was photodegraded in domestic wastewater which was simultaneously disinfected for total coliform bacterial (TCB) (360 min) and Escherichia coli (60 min).
Graphical abstract TCC degradation and ecotoxicological assessment
  相似文献   
105.
The degradation of sulfamonomethoxine (SMM) in the aqueous environment by the combination of UV illumination and Oxone has been studied. Experimental results indicated that the UV illumination can effectively activate Oxone to produce sulfate-free radicals (SO4 ??). When 10 mmol L?1 Oxone was added, 96.78 % removal of SMM (5 mg L?1) was achieved within 90 min. Mineralization of SMM was investigated by measuring the total organic carbon, which decreased by 89.01 % after 90 min reaction. Six intermediate compounds generated during the SMM degradation were identified with the aid of liquid chromatography and mass spectroscopy, combined with proton nuclear magnetic resonance spectroscopy. A general reaction pathway for the degradation of SMM was proposed, where the presence of SO4 ?? remained crucial during the degradation process.  相似文献   
106.
为了提高厌氧流化床微生物燃料电池(AFB-MFC)的性能,并为双室MFC寻找价廉、易得、无污染的阴极液,在曝气量16~24 L/h、温度(35±2)℃、回流量10.2 L/h、阴极底边距阴极室内底部17.3 cm、外电阻250 Ω、水力停留时间(HRT)14.0~14.9 h以及进水pH 7.81~8.37下,研究了阴极液及底物浓度对系统产电及废水处理性能的影响。结果表明,使用缓冲溶液、阳极室出水和自来水作阴极液时,自来水的产电性能最佳,阴极液种类不影响系统有机基质的去除。以自来水为阴极液时,阴极液pH及电导率随运行时间增加而增加,COD去除率为80.11%~89.29%,输出电压及功率密度开始随运行时间增加而增加,之后稳定在440~452 mV和48.40~51.08 mW/m2之间。增加底物浓度对COD去除率影响不大,而输出电压及功率密度随底物浓度增加而下降;底物COD浓度由3 307.09 mg/L增至9 520 mg/L时,COD去除率在85.77%~94.44%之间,输出电压及功率密度则分别由449 mV和50.40 mW/m2下降至406 mV和41.21 mW/m2。自来水作阴极液可避免二次污染及阴极液对阳极室微生物的影响,并得到高的产电能力。  相似文献   
107.
More than 25 studies have employed land use regression (LUR) models to estimate nitrogen oxides and to a lesser extent particulate matter indicators, but these methods have been less commonly applied to ambient concentrations of volatile organic compounds (VOCs). Some VOCs have high plausibility as sources of health effects and others are specific indicators of motor vehicle exhaust. We used LUR models to estimate spatial variability of VOCs in Toronto, Canada. Benzene, n-hexane and total hydrocarbons (THC) were measured from July 25 to August 9, 2006 at 50 locations using the TraceAir organic vapor monitors. Nitrogen dioxide (NO2) was also sampled to assess its spatial pattern agreement with VOC exposures. Buffers for land use, population density, traffic density, physical geography, and remote sensing measures of greenness and surface brightness were also tested. The remote sensing measures have the highest correlations with VOCs and NO2 levels (i.e., explains >36% of the variance). Our regression models explain 66–68% of the variance in the spatial distribution of VOCs, compared to 81% for the NO2 model. The ranks of agreement between various VOCs range from 48 to 63% and increases substantially – up to 75% – for the top and bottom quartile groups. Agreements between NO2 and VOCs are much smaller with an average rank of 36%. Future epidemiologic studies may therefore benefit from using VOCs as potential toxic agents for traffic-related pollutants.  相似文献   
108.
介绍了中小型工业窑炉生产过程中排放NOx的现状,并针对NOx的治理问题,从工程应用角度,简述了湿法和干法净化NOx的原理和化学反应过程。讨论了NOx排放特性和NOx废气中NO2/NOx比例的问题。提出了影响NOx治理的主要因素,包括吸收剂、吸附剂、催化剂和设备的部分应用参数,并结合工程实例指出工程需要注意的问题。介绍了多项采用湿法和干法净化NOx的工程应用项目,丰富了中小工业窑炉NOx废气的治理的实践经验,为中小工业窑炉排放NOx治理奠定了基础。  相似文献   
109.
This study aims to develop a methodology for analysis of characteristics of heavy metals in MSWI fly ash. It performed analysis of composition of heavy metals, leaching toxicity, leaching behavior as a function of pH, specification distribution and corresponding mineral components of residue derived from each step of the sequential extraction. It is found that content of heavy metals follows the sequence of Zn > Pb > Cu > Cr > As > Ni > Cd approximately Hg in both plants, and that total heavy metals account for less than 1% by mass of fly ash. Major hazardous heavy metals in fly ash are As, Cd, Hg, Pb and Zn, whose leaching ratios exceed the limit value described in hazardous waste identification standard. Measured leaching results of Cu, Pb and Zn are essentially consistent with the simulated results at pH between 0 and 13. Content of calcium-silicates, alumino-silicates and glass phases in residue derived from sequential extraction procedure increases steadily from the first step to the fifth step of the sequential extraction procedure. Cu, As, Cr, Hg, Cd, and Ni, relatively stable under strong basic conditions, can be leached out under strong acidic conditions, while Zn and Pb tend to be leached out under both strong acidic and basic conditions.  相似文献   
110.
树脂吸附-Fenton 试剂氧化法预处理炼油碱渣废水   总被引:1,自引:0,他引:1  
采用树脂吸附-Fenton 试剂氧化组合工艺对某炼油企业炼油碱渣废水进行预处理.实验确定的最佳工艺条件为:3 种树脂串联吸附,废水流量0.33 mL/ min,H2O2加入量0.20 mol / L,n(H2O2)1 n(Fe2 +)= 12,Fenton 试剂氧化进水pH 3,Fenton 试剂氧化反应时间120 m...  相似文献   
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