A novel, functionalized bubble surface can be obtained in dissolved air flotation (DAF) by dosing chemicals in the saturator. In this study, different cationic chemicals were used as bubble surface modifiers, and their effects on natural organic matter (NOM) removal from river water were investigated. NOM in the samples was fractionated based on molecular weight and hydrophobicity. The disinfection byproduct formation potentials of each fraction and their removal efficiencies were also evaluated. The results showed that chitosan was the most promising bubble modifier compared with a surfactant and a synthetic polymer. Tiny bubbles in the DAF pump system facilitated the adsorption of chitosan onto microbubble surfaces. The hydrophobic NOM fraction was preferentially removed by chitosan-modified bubbles. Decreasing the recycle water pH from 7.0 to 5.5 improved the removal of hydrophilic NOM with low molecular weight. Likewise, hydrophilic organic compounds gave high dihaloacetic acid yields in raw water. An enhanced reduction of haloacetic acid precursors was obtained with recycle water at pH values of 5.5 and 4.0. The experimental results indicate that NOM fractions may interact with bubbles through different mechanisms. Positive bubble modification provides an alternative approach for DAF to enhance NOM removal.
CoFe2O4/ordered mesoporous carbon (OMC) nanocomposites were synthesized and tested as heterogeneous peroxymonosulfate (PMS) activator for the removal of rhodamine B. Characterization confirmed that CoFe2O4 nanoparticles were tightly bonded to OMC, and the hybrid catalyst possessed high surface area, pore volume, and superparamagnetism. Oxidation experiments demonstrated that CoFe2O4/OMC nanocomposites displayed favorable catalytic activity in PMS solution and rhodamine B degradation could be well described by pseudo-first-order kinetic model. Sulfate radicals (SO4−·) were verified as the primary reactive species which was responsible for the decomposition of rhodamine B. The optimum loading ratio of CoFe2O4 and OMC was determined to be 5:1. Under optimum operational condition (catalyst dosage 0.05 g/L, PMS concentration 1.5 mM, pH 7.0, and 25 °C), CoFe2O4/OMC-activated peroxymonosulfate system could achieve almost complete decolorization of 100 mg/L rhodamine B within 60 min. The enhanced catalytic activity of CoFe2O4/OMC nanocomposites compared to that of CoFe2O4 nanoparticles could be attributable to the increased adsorption capacity and accelerated redox cycles between Co(III)/Co(II) and Fe(III)/Fe(II).
A triple-objective optimal sizing method based on a dynamic strategy is presented for an islanded hybrid energy microgrid, consisting of wind turbine, solar photovoltaic, battery energy storage system and diesel generator. The dynamic strategy is given based on a dynamic complementary coordination between two different master-slave control modes for maximum renewable energy utilization. Combined with the proposed strategy, NSGA-II-based optimization program is applied to the sizing optimization problem with triple different objectives including the minimization of annualized system cost, the minimization of loss of power supply probability and the maximization of utilization ratio of renewable energy generation. The sizing results and the proposed strategy are both compared and analyzed to validate the proposed method in a real case of an islanded hybrid energy microgrid on Dong’ao Island, China. 相似文献
Zeolite-carbon composites (Na-P1(C), Na-X(C)) and pure zeolites (Na-P1, Na-X) were synthesized from hazardous high-carbon fly ash waste (HC FA) via hydrothermal reaction with sodium hydroxide (NaOH). These solids were applied in the removal of diclofenac (DCF) from aqueous solution, with and without poly(acrylic acid) (PAA). The experiments included adsorption–desorption measurements, as well as electrokinetic and stability analyses. The obtained results showed that HC FA and Na-P1(C) had the greatest adsorption capacity towards DCF, i.e., 26.51 and 21.19 mg/g, respectively. PAA caused considerable decrease in the DCF adsorption due to the competition of both adsorbates of anionic character for active sites. For example, the adsorbed amount of DCF on Na-P1 without PAA was 14.11 mg/g, whereas the one measured with PAA was 5.08 mg/g. Most of prepared solids were effectively regenerated by the use of NaOH. Desorption degree reached even 73.65% in the single systems (with one adsorbate) and 97.24% in the mixed ones (with two adsorbates). Zeolitic materials formed suspensions of rather low stability, which underwent further deterioration in the organic molecules presence. All the results obtained in this study indicated that HC FA can be successfully managed in the removal of organic substances.
A technique is presented to solve analytically the turbulent diffusion equation for the concentration of a passive contaminant
emitted from an elevated continuous source into the atmosphere. A generalized method of solution using Sturm–Liouville and
WKB theories is developed to overcome difficulties due to the height‐dependent wind velocity and diffusion coefficient appearing
in the diffusion equation. The method presented in this paper is able to derive an asymptotic expression for the concentration
obtained from the solution of the atmospheric diffusion equation which involves explicitly inhomogeneous wind velocity and
diffusion coefficient. The diffusion equation model derived from this method can be applied in a practical prediction of contaminant
concentration in a turbulent atmosphere.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
Journal of Material Cycles and Waste Management - Waste classification is comprehensively carried out in China as an important national-level policy, and the large amount and the wide range of food... 相似文献