Key role of •O2- in promoting deep degradation of VOCs in VUV-based process.

VUV photolysis presents a simple process for VOCs degradation, while the poor mineralization rate and extensive by-products greatly limit its application. In this study, the contribution and synergy between •OH and •O2- to toluene degradation in the VUV-based process were comprehensively investigated by controlling water and oxygen in the gas flow. It was found that •OH promoted the initial degradation of toluene and macromolecular intermediates, while •O2- dominated toluene mineralization by boosting the formation of small molecules and CO2. Compared with the •OH-dominated VUV photolysis, the presence of catalyst greatly changed the degradation pathway, promoted toluene mineralization into CO2 and reduced health toxicity via promoting •O2- formation. This study originally focuses on the key role of •O2- in VOCs deep oxidation and provides an effective strategy to boost its clean mineralization via the VUV-based process.

BiVO4 prepared by the sol-gel doped on graphite felt cathode for ciprofloxacin degradation and mechanism in solar-photo-electro-Fenton.

In this research, bismuth vanadate-doped graphite felt (GF-BiVO4) was successfully prepared by sol-gel method, in which BiVO4 owned superior electro-Fenton (EF) and solar-photo-electro-Fenton (SPEF) performance. Combined with the analysis by X-ray diffractometer (XRD), field emission transmission electron microscopy (FE-TEM), nitrogen adsorption-desorption isotherms and cyclic voltammetry (CV), the changes of electrodes were reflected in structure and physicochemical properties. The doping of monoclinic BiVO4 endued GF with a higher surface area and more electro-active sites and better electrode activity in comparison to Raw-GF. Then, the GFs were used as cathodes to detect •OH concentration with coumarin (COU) as probe molecule and to evaluate photoelectric performance with ciprofloxacin (CIP) in photocatalysis, EF and SPEF processes. The results demonstrated that the concentration of •OH followed an order of SPEF> EF> photocatalysis, which was consistent with the removal rate of CIP (99.8%, 99.4% and 21.2%, respectively) on GF-BiVO4 at 5 min. Further, five degradation pathways of CIP in SPEF system were proposed including the attack on piperazine ring, oxidation on cyclopropyl group, decarboxylation and hydroxyl radical addition, oxidation on benzene group and defluorination. The study provides insights into the enhancement of EF and SPEF performance and the degradation pathway of CIP in SPEF.

Kinetics and mechanisms of oxytetracycline degradation in an electro-Fenton system with a modified graphite felt cathode.

The removal of trace antibiotics from the aquatic environment has received great interest. In this investigation, NaOH activated graphite felt (NaOH-GF) was characterized by multiple-methods, including scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), contact angle, linear sweep voltammetry (LSV) and electron paramagnetic resonance (EPR). The NaOH-GF was then used as the cathode in the electro-Fenton process for oxytetracycline (OTC) degradation, the experiment was carried out in an undivided and light-proof beaker with a Pt anode and a NaOH-GF cathode at pH 3. The results showed that the modification with NaOH enhanced the antibiotics degradation efficiency of graphite felt by increasing the oxygen reduction capacity and hydroxyl radicals yielding rate. Complete OTC removal was achieved at 5.17 mA cm-2 after 40, 60 and 90 s with initial OTC concentration of 22, 44, and 66 µM, respectively. With an initial OTC concentration of 44 µM, after 30 min the removal rates of chemical oxygen demand (COD) by Raw-GF and NaOH-GF were 59.18% and 83.75%, respectively. The proposed degradation mechanism of OTC was an EF process, which consisted of hydroxylation, secondary alcohol oxidation, demethylation, decarbonylation, dehydration and deamination. This study demonstrates that NaOH activated GF cathode possesses high degradation capacity and good stability. It provides insight into the removal of non-biodegradable antibiotics and may shed light on future to its practical application.

Optimization of kinetics and operating parameters for the bioleaching of heavy metals from sewage sludge, using co-inoculation of two Acidithiobacillus species.

This study explores the potential for synchronous extraction of Cu, Cr, Ni and Zn during sewage sludge bioleaching processes, using three types of bacterial cultures: a pure culture of Acidithiobacillus ferrooxidans (A. ferrooxidans); a pure culture of Acidithiobacillus thiooxidans (A. thiooxidans); and a mixed culture of A. ferrooxidans and A. thiooxidans. Variable operating parameters included initial pH, solids concentration, sulfur concentration and ferrous iron concentration, with optimization via Box-Behnken design of response surface methodology. Results indicate that the mixed culture of A. ferrooxidans and A. thiooxidans, was the most effective at bioleaching heavy metals from sewage sludge. The optimal operating conditions were as follows: an initial pH of 2.0, with concentrations of 3% solids, 6.14 g L-1 sulfur and 4.55 g L-1 ferrous iron. Maximum extraction efficiencies obtained after 14 days of bioleaching under optimal conditions, were 98.54% Cu, 57.99% Cr, 60.06% Ni and 95.60% Zn. Bioleaching kinetics were effectively simulated using a shrinking core model to explain the leaching reaction, with modelling results suggesting that the rate was determined by the diffusion step.