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61.
Pan G Zhang MM Chen H Zou H Yan H 《Environmental pollution (Barking, Essex : 1987)》2006,141(2):195-200
Algal removal abilities of 26 clays/minerals were classified into three categories according to the 8-h equilibrium removal efficiency (Q8h) and removal rate at a clay loading of 0.7 g/L. Type I clays (sepiolite, talc, ferric oxide, and kaolinite) had a Q8h > 90%, a t50 (time needed to remove 50% of the algae) < 15 min, and a t80 < 2.5 h. Type II clays (6 clays) had a Q8h 50-90%, a t50 < 2.5 h, and a t80 > 2.5 h. Type III clays (14 clays) with Q8h < 50%, t50 > 8 h and t80 > 14 h had no practical value in removal of algal blooms. When the clay loading was reduced to 0.2 g/L, Q8h for all the 25 materials decreased to below 60%, except for sepiolite whose Q8h remained about 97%. The high efficiency for sepiolite to flocculate M. aeruginosa cells in freshwaters was due to the mechanism of netting and bridging effect. 相似文献
62.
柱生物曝气法吸附处理含铬废水 总被引:7,自引:0,他引:7
利用复合生物吸附剂FY01与活性污泥作为吸附材料,探讨了柱式生物曝气法对高浓度含铬电镀废水的生物吸附效果。研究结果表明,FY01性能稳定,耐进水pH冲击能力较强。当进水pH=2—5、流速为500mL/h时,10gFY01和5g活性污泥联合处理60.4mg/L含铬电镀废水2h后,铬的去除率达78%以上;在4℃冰箱和23—28℃实验室保存50d的FY01对铬的去除分别在78%~83%和77%-84%之间。柱式生物曝气吸附法对含铬废水的处理效果理想,运行稳定。串联处理2000mL总Cr、Cu^2+和COD浓度分别为60.4、4.51和48.2mg/L的电镀废水2h后,去除率分别高达92.1%、99.2%和71.4%。 相似文献
63.
高级氧化法脱除PVA浆料的清洁生产新工艺研究 总被引:3,自引:0,他引:3
为了研究高级氧化法脱除聚乙烯醇(PVA)浆料清洁生产新工艺的可行性,研究了3种高级氧化法UV/H2O2、UV/TiO2、Nation-Fe^2+/H2O2对含PVA溶液的氧化降解,其降解效果依次为iUV/H2O2〉Nation-Fe^2+/H2O2〉UV/TiO2。对于UV/H2O2法,PVA降解速率与H2O2的初始浓度成正相关,且H2O2浓度为2.95mmol/L时14min内就能使PVA的去除率达到98%;pH和温度对PVA的氧化降解效果影响不明显。在此基础上,对建立在高级氧化法基础上的退浆新工艺进行了探讨,结果表明,在65℃和75℃下,高级氧化法条件下的纯棉织物PVA退浆率分别达到70.16%和95.65%;该法不仅可以促进PVA从纯棉织物上的脱附,而且可以达到对PVA的较高降解效果,使得所排退浆废水的生化处理难度明显降低。 相似文献
64.
Status of trace elements in paddy soil and sediment in Taihu Lake region 总被引:14,自引:0,他引:14
Thirteen paddy soil profiles and river sediments which are sources of irrigation water were collected around the Taihu Lake, and the trace elements were estimated. The content of La and Ce in paddy soil and sediment were 39.3 and 68.6 mg/kg soil and 36.9 and 65.1 mg/kg soil, being within the range of background values. The values for Pb, Cu, Ni, Cr, Co, Mn, Zn, Se in paddy soil were 23.3, 27.8, 25.5, 63.5, 10.2, 386, 68.7 and 0.25 mg/kg soil respectively, all below the national permission level. There was a decline of Zn in paddy soil. Some of the river sediments were seriously polluted. The river in Yangjin site was most contaminated with 5.47 g Cu/kg and 7.4 g Zn/kg. The high concentration of Pb and Ni also was observed in this sediment. River in Weitang, Huashi, Xinzhuang and Meiyan were contaminated with Pb, Cu and Ni to some extent. Zn, Cu and Pb were the main pollutants in present experiment sites. The fast development of village/township industries have caused severe environmental pollution in the Taihu Lake region, especially irrigation river sediments. Se content in plant and seed was 0.04 and 0.03 mg/kg respectively, showed Se-deficiency in paddy soil in the Taihu Lake region. 相似文献
65.
Ling R. Zeng Li H. Shi Xin G. Meng J. Xu Gui F. Jia T. Gui 《Journal of environmental science and health. Part. B》2019,54(4):317-325
This study evaluated the hydrolysis and photolysis kinetics of pyraclostrobin in an aqueous solution using ultra-high-performance liquid chromatography–photodiode array detection and identified the resulting metabolites of pyraclostrobin by hydrolysis and photolysis in paddy water using high-resolution mass spectrometry coupled with liquid chromatography. The effect of solution pH, metal ions and surfactants on the hydrolysis of pyraclostrobin was explored. The hydrolysis half-lives of pyraclostrobin were 23.1–115.5?days and were stable in buffer solution at pH 5.0. The degradation rate of pyraclostrobin in an aqueous solution under sunlight was slower than that under UV photolysis reaction. The half-lives of pyraclostrobin in a buffer solution at pH 5.0, 7.0, 9.0 and in paddy water were less than 12?h under the two light irradiation types. The metabolites of the two processes were identified and compared to further understand the mechanisms underlying hydrolysis and photolysis of pyraclostrobin in natural water. The extracted ions obtained from paddy water were automatically annotated by Compound Discoverer software with manual confirmation of their fragments. Two metabolites were detected and identified in the pyraclostrobin hydrolysis, whereas three metabolites were detected and identified in the photolysis in paddy water. 相似文献
66.
Ting Gui Gui F. Jia Jin Xu Shi J. Ge Xiao F. Long 《Journal of environmental science and health. Part. B》2019,54(4):326-335
A modified quick, easy, cheap, effective, rugged and safe (QuEChERS) method was developed for the determination of thiamethoxam and its metabolite clothianidin in citrus (including the whole citrus, peel and pulp) and soil samples by liquid chromatography-tandem mass spectrometry. The sample was extracted with acetonitrile and purified with octadecylsilane. The detection limits of both compounds were 0.0001–0.0002?mg kg–1, while the limit of quantification of thiamethoxam was 0.002?mg kg–1 and the limit of quantitation of metabolites was 0.001?mg kg–1. The recovery was 70.37%–109.76%, with inter-day relative standard deviations (RSD) (n?=?15) values ≤9.46% for the two compounds in the four matrices. The degradation curve of thiamethoxam in whole citrus and soil was plotted using the first-order kinetic model. The half-life of the whole citrus was 1.9–6.2?days, and the half-life of the soil was 3.9–4.2?days. The terminal residue of thiamethoxam (the sum of thiamethoxam and clothianidin, expressed as thiamethoxam) was found to be concentrated on the peel. The final residual amount of thiamethoxam in the edible portion (pulp) was less than 0.061?mg kg–1. The risk quotient values were all below 1, indicating that thiamethoxam as a citrus insecticide does not pose a health risk to humans at the recommended dosage. 相似文献
67.
Guo Jun-Xiong Pan Jie Wang Jing Wang Fei Shi Hong-Xin 《Environmental science and pollution research international》2019,26(20):20499-20509
Environmental Science and Pollution Research - Drinking water containing environmental endocrine disruptor compounds (EDCs) endangers human health, and researching the purification process of... 相似文献
68.
Singh RB Huber AH Braddock JN 《Journal of the Air & Waste Management Association (1995)》2003,53(10):1204-1217
The U.S. Environmental Protection Agency's National Exposure Research Laboratory is pursuing a project to improve the methodology for modeling human exposure to motor vehicle emissions. The overall project goal is to develop improved methods for modeling the source through the air pathway to human exposure in significant exposure microenvironments. Current particulate matter (PM) emission models, particle emission factor model (used in the United States, except California) and motor vehicle emission factor model (used in California only), are suitable only for county-scale modeling and emission inventories. There is a need to develop a site-specific real-time emission factor model for PM emissions to support human exposure studies near roadways. A microscale emission factor model for predicting site-specific real-time motor vehicle PM (MicroFacPM) emissions for total suspended PM, PM less than 10 microm aerodynamic diameter, and PM less than 2.5 microm aerodynamic diameter has been developed. The algorithm used to calculate emission factors in MicroFacPM is disaggregated, and emission factors are calculated from a real-time fleet, rather than from a fleet-wide average estimated by a vehicle-miles-traveled weighting of the emission factors for different vehicle classes. MicroFacPM requires input information necessary to characterize the site-specific real-time fleet being modeled. Other variables required include average vehicle speed, time and day of the year, ambient temperature, and relative humidity. 相似文献
69.
70.