Hydrodynamic conditions are important factors for planktonic algae growth, through introducing two parameters which express the optimal velocity and the velocity range for planktonic algae growth, a new velocity factor was put forward for the formula of growth rate. Therefore, the two-dimensional unsteady ecological dynamic model for algae growth was established to analyze the effects of hydrodynamic conditions on algae growth in Chongqing Reach of Jialing River in China. The temporal and spatial distribution of Chlorophyll-a (Chl-a) concentration was simulated numerically for various water levels, under climate conditions in period of high frequency for algae blooms of Three Gorges Reservoir and nutrition status at present in the research reach. The corresponding locations and areas of likely algae blooms were analyzed and forecasted. The results showed that about 0.04 m s−1 was the optimal velocity for algae growth, and the occurrence of algae blooms in large scale is almost impossible because of relatively high water flow velocity for Jialing River. 相似文献
The adsorption of sulfadiazine onto kaolinite clay as an alternative adsorbent was examined in aqueous solution, hnpacts of the contact time, pH, temperature, ionic strength and coexistent surfactants on the adsorption process were evaluated. The pH significantly influenced the adsorption process, with adsorption being promoted at lower pH due to the cation exchange mechanism. Decreasing ionic strength in the solution was favorable for adsorption, and the addition of cationic and anionic surfactants had negative effects on the adsorption capacity of sulfadiazine on kaolinite. Kinetic experiments showed that the adsorption followed the pseudo-second-order model. The equilibrium adsorption was well described by both Freundlich and Dubinin-Radushkevich (DR) models. According to the DR model, the adsorption mechanism was determined by cationic exchange and weak physical forces. The thermodynamic study showed that sulfadiazine adsorption onto kaolinite was a sponta- neous and endothermic reaction. 相似文献
Water contamination by emerging organic pollutants is calling for advanced methods of remediation such as iron-activated sulfite-based advanced oxidation. Sulfate radical, SO4??, and hydroxyl radical, ?OH, are the primary reactive intermediates formed in the Fe(III)/sulfite system, yet the possible involvement of Fe(IV) produced from Fe(II) and persulfates is unclear. Here we explored the role of Fe(IV) in the Fe(III)/sulfite system by methyl phenyl sulfoxide (PMSO) probe assay, electron paramagnetic resonance spectra analysis, alcohol scavenging experiment, and kinetic simulation. Results show that PMSO is partially transformed into methyl phenyl sulfone (PMSO2), thus evidencing Fe(IV) formation. The remaining degradation of PMSO is due to SO4?? and ?OH. The contribution of Fe(IV) versus free radicals is progressively promoted when the Fe(III)-sulfite reaction proceeds, with an upper limit of 80–90%. The contribution of Fe(IV) versus free radicals increases with Fe(III) and sulfite dosages, and decreases with increasing pH. Overall, our findings demonstrate the involvement of Fe(IV) in the Fe-catalyzed sulfite auto-oxidation process.