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1.
Chemosphere ; 325: 138423, 2023 Jun.
Article in English | MEDLINE | ID: mdl-36934480

ABSTRACT

Recently, there are still some controversial mechanisms of the 3D electrocatalytic oxidation system, which would probably confound its industrial application. From the conventional viewpoint, the Ti4O7 material may be the desired particle electrodes in the 3D system since its high oxygen evolution potential favors the production of •OH via H2O splitting reaction at the anode side of Ti4O7 particle electrodes. In fact, the incorporation of Ti4O7 particles showed phenol degradation of 88% and COD removal of 51% within 120 min, under the optimum conditions at energy consumption of 0.668 kWh g-1 COD, the performance of which was much lower than those in many previous literatures. In contrast, the prepared carbon black-polytetrafluoroethylene composite (CB-PTFE) particles with abundant oxygen-containing functional groups could yield considerable amounts of H2O2 (200 mg L-1) in the 3D reactor and achieved a complete degradation of phenol and COD removal of 80% in the presence of Fe2+, accompanying a low energy consumption of only 0.080 kWh g-1 COD. It was estimated that only 20% of Ti4O7 particles near the anode attained the potential over 2.73 V/SCE at 30 mA cm-2 based on the potential test and simulation, responsible for the low yield of •OH via the H2O splitting on Ti4O7 (1.74 × 10-14 M), and the main role of Ti4O7 particle electrodes in phenol degradation was through direct oxidation. For the CB-PTFE-based 3D system, current density of 10 mA cm-2 was sufficient for all the CB-PTFE particles to attain cathodic potential of -0.67 V/SCE, conducive to the high yield of H2O2 and •OH (9.11 × 10-14 M) in the presence of Fe2+, and the •OH-mediated indirect oxidation was mainly responsible for the phenol degradation. Generally, this study can provide a deep insight into the 3D electrocatalytic oxidation technology and help to develop the high-efficiency and cost-efficient 3D technologies for industrial application.


Subject(s)
Hydrogen Peroxide , Water Pollutants, Chemical , Water Pollutants, Chemical/analysis , Phenols , Phenol , Oxidation-Reduction , Electrodes
2.
Spectrochim Acta A Mol Biomol Spectrosc ; 59(7): 1605-10, 2003 May.
Article in English | MEDLINE | ID: mdl-12714083

ABSTRACT

The interactions between daunorubicin and human serum albumin (HSA) were studied using the spectrofluorimetric method. The binding constants of daunorubicin with HSA were obtained at different temperatures. The effects of various metal ions on the binding constants of daunorubicin with HSA were also studied. The optimum conditions of fluorometric determination of daunorubicin were studied and the developed method was successfully applied to the determination of daunorubicin in serum samples.


Subject(s)
Daunorubicin/blood , Serum Albumin/metabolism , Blood Chemical Analysis/methods , Energy Transfer , Humans , In Vitro Techniques , Kinetics , Metals/pharmacology , Protein Binding/drug effects , Spectrometry, Fluorescence/methods , Temperature
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