Two fresh refuse bioreactors (F1 and F2) were operated under semi-aerobic and anaerobic conditions, respectively. The leachate from the bioreactors F1 and F2 was introduced into the aged refuse bioreactors (A1 and A2), and the effluent from A1 and A2 was subsequently recirculated into F1 and F2, respectively. The effect of the semi-aerobic recirculation process on refuse degradation was investigated, comparing it with that of the anaerobic recirculation process. Results indicate that the semi-aerobic recirculation process can increase the accumulated net production of leachate and promote evaporation. The accumulated net production of refuse in F1 is 320 mL/kg and that of F2 is 248 mL/kg, with leachate reduction amounting to 315 and 244 mL/kg refuse, respectively. The leachate quantity reduction of semi-aerobic and anaerobic leachate recirculation process accounted for 98.4% and 98.3% of the accumulated net production of leachate, respectively. The semi-aerobic leachate recirculation process can improve the biodegradation of organic matter from fresh refuse and the reduction rate of the pollutant concentration in leachate. This should shorten considerably the time required to meet the discharge standard and the time of stabilization of the refuse as observed in the anaerobic recirculation process. It was predicted that the COD concentration of leachate from the anaerobic recirculation process would reach 1000 mg/L in the anaerobic recirculation process after 2.2 years, as for semi-aerobic leachate recirculation process it is about 100 days. Compared with anaerobic recirculation process, the semi-aerobic recirculation process is more effective on NH3-N transformation and TN removal. The NH3-N and TN concentration of F1 is far below those of F2 at the end of our experiment. Refuse settlement in the semi-aerobic recirculation process was faster than that in the anaerobic recirculation process. At the end of the experiment, refuse settlement ratios in the semi-aerobic and anaerobic bioreactors were 33.5% and 18%, respectively. 相似文献
It has been shown that starch can effectively stabilize nanoscale magnetite particles, and starch-stabilized magnetite nanoparticles (SMNP) are promising for in situ remediation of arsenic-contaminated soils. However, a molecular level understanding has been lacking. Here, we carried out XAFS studies to bridge this knowledge gap. Fe K-edge XAFS spectra indicated that the Fe-O and Fe-Fe coordination numbers of SMNP were lower than those for bare magnetite particles, and these coordination numbers decreased with increasing starch concentration. The decrease in the average coordination number at elevated stabilizer concentration was attributed to the increase in the surface-to-volume ratio. Arsenic K-edge XAFS spectra indicated that adsorbed arsenate on SMNP consisted primarily of binuclear bidentate (BB) complexes and monodentate mononuclear (MM) complexes. More BB complexes (energetically more favorable) were observed at higher starch concentrations, indicating that SMNP not only offered greater adsorption surface area, but also stronger adsorption affinity toward arsenate. 相似文献
Environmental Science and Pollution Research - The pollution of heavy metals is a severer problem for the ecosystems in waters. The toxicity of Cd2+ on phycocyanin (PC) is studied in molecular... 相似文献
AbstractMulti-spectroscopic and molecular docking methods were used to study the interaction between triclosan (TCS) and bovine serum albumin (BSA). The results indicated that the fluorescence quenching of BSA by TCS was due to the formation of TCS–BSA complex through static quenching. This result was also demonstrated by time-resolved fluorescence experiment. The binding constants and number of binding sites between TCS and BSA were 1.30?×?105 M?1 and 1.17 at 298?K, respectively. The thermodynamic parameters were studied in detail which suggested that hydrophobic forces and hydrogen bond played major roles in the TCS–BSA interaction. Moreover, the site marker competitive experiments and docking studies revealed that TCS could bind BSA into site I in subdomain IIA. All the results of UV–vis spectrophotometry, circular dichroism spectroscopy and synchronous fluorescence spectroscopy showed that interaction between TCS and BSA induced conformation changes of BSA. 相似文献
Environmental Science and Pollution Research - In this study, the immature mice were taken to assess the potential neurological toxicity of lead (Pb) and di (n-butyl) phthalates (DBP) combination... 相似文献
Efficient abatement of an iodinated X-ray contrast media iohexol by an emerging sulfite autoxidation advanced oxidation process is demonstrated, which is based on transition metal ion–catalyzed autoxidation of sulfite to form active oxidizing species. The efficacy of the combination of sulfite and transition metal ions (Ag(I), Mn(II), Co(II), Fe(II), Cu(II), Fe(III), or Ce(III)) was tested for iohexol abatement. Co(II) and Cu(II) are proven to show more pronounced catalytic activity than other metals at pH 8.0. According to the quenching studies, sulfate radical (SO4??) is identified to be the primary species for oxidation of iohexol. Increasing dosages of metal ion or sulfite and higher pH values are favorable for iohexol abatement. Inhibition of iohexol abatement is observed in the absence of dissolved oxygen, which is vital for the production of SO5?? and subsequent formation of SO4??. Overall, activation of sulfite to produce reactive radicals with extremely low Co(II) or Cu(II) concentrations (in the range of μg L?1) in circumneutral conditions is confirmed, which offers a potential SO4??-based advanced oxidation process in treatment of aquatic organic contaminants.