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Biological aerated filters (BAFs) are widely used for the treatment of micropolluted surface water. However, the biological process produces dissolved organic nitrogen (DON), which, as precursors of nitrogenous disinfection by-products, pose potential threats to drinking water safety. Therefore, to control DON in BAF effluent, it is necessary to study the influence of BAF operation parameters on DON production. In this study, the influence of filtration velocity in a BAF on DON production was investigated. Under different filtration velocity (0.5, 2, and 4 m/h) conditions, profiles of DON concentrations along the media layer were measured. The profile at a filtration velocity of 0.5 m/h showed a decreasing trend, and the ones under filtration velocities of 2 and 4 m/h fluctuated in a small range (from 0.1 to 0.4 mg/L). Moreover, the relatively high filtration velocities of 2 and 4 m/h resulted in a lower level of DON concentration. Additionally, 3D excitation-emission matrix fluorescence spectroscopy was used to characterize DON. It is found that the patterns of DON at a relatively high filtration velocity condition (4 m/h) were obviously different from the ones under low filtration velocity conditions (0.5 and 2 m/h).  相似文献   
2.
Radiation-induced degradation of methyl orange in aqueous solutions   总被引:1,自引:0,他引:1  
Chen YP  Liu SY  Yu HQ  Yin H  Li QR 《Chemosphere》2008,72(4):532-536
Degradation of methyl orange under gamma-irradiation was investigated. The reactions followed pseudo first-order kinetics. Apparent degradation rate constant, estimated through linear regression analysis, increased with an increase of dose rate and a decrease of initial methyl orange concentration. Degradation of methyl orange was significantly accelerated under oxidative condition, but was slightly enhanced under reductive condition. However, the result of decoloration was better under reductive condition than oxidative one. An analysis on the intermediates using Fourier transform infrared and gas chromatography/mass spectrometry demonstrates that the radiolytic degradation of methyl orange was processed with different C-N cleavages under oxidative and reductive conditions.  相似文献   
3.
Kinetics and mechanisms of radiation-induced degradation of acetochlor   总被引:7,自引:0,他引:7  
Liu SY  Chen YP  Yu HQ  Zhang SJ 《Chemosphere》2005,59(1):13-19
The radiation-induced degradation of acetochlor was investigated in this work. In a mixed solvent composed of acetonitrile and water at a ratio of 20/80 in volume, the acetochlor degradation rate was proportional to the radiation dose rate and acetochlor concentration. The acetochlor degradation efficiency was higher under alkali conditions and lower under acidic conditions. The contribution to the acetochlor degradation by the radicals was in the order of: e(aq)->.OH>H.. The quantum efficiency ratios of .OH, e(aq)- and H. for the degradation of acetochlor were calculated as 1:3:1.  相似文献   
4.

A pilot-scale side-stream reactor process with single-stage sludge alkaline treatment was employed to systematically investigate characteristics of excess sludge hydrolysis and acidification with alkaline treatment and evaluate feasibility of recovering a carbon source (C-source) from excess sludge to enhance nutrient removal at ambient temperature. The resulting C-source and volatile fatty acid specific yields reached 349.19 mg chemical oxygen demand (COD)/g volatile suspended solids (VSS) d−1 and 121.3 mg COD/g VSS d−1, respectively, the process had excellent C-source recovery potential. The propionic-to-acetic acid ratio of the recovered C-source was 3.0 times that in the influent, which beneficially enhanced biological phosphorus removal. Large populations and varieties of hydrolytic acid producing bacteria cooperated with alkaline treatment to accelerate sludge hydrolysis and acidification. Physicochemical characteristics indicated that recovered C-source was derived primarily from extracellular polymeric substances hydrolysis rather than from cells disruption during alkaline treatment. This study showed that excess sludge as carbon source was successfully recycled by alkaline treatment in the process.

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