Hybridizing Ag-Doped ZnO nanoparticles with graphite as potential photocatalysts for enhanced removal of metronidazole antibiotic from water.

In this study, the ZnO nanoparticles were doped with Ag and then hybridized on graphite (GP) layer (Ag-ZnO/GP) by a hydrothermal method, which was used as photocatalysts to remove metronidazole (MNZ) antibiotic from aqueous solutions. The fine structure, morphologies, and optical properties of the synthesized composites were first examined. The incorporation of Ag would readily reduce the rate of the recombination of electron-hole pairs and enhance the photocatalytic activity in a wide range of light wavelength. The graphite surface also acted as an electron sink to efficiently inhibit the photocorrosion of ZnO, thereby improving the photostability of the composites. The composition of the composite was optimized to be 0.5 wt% GP/ZnO and 1.0 wt% Ag/ZnO according to the extent of the enhancement of photocatalytic activity. In a solution containing 30 mg L-1 of MNZ and 0.5 g L-1 of Ag-ZnO/GP composite, it was shown that 88.5% and 97.3% of MNZ was removed after 60 min of 100-W UV and 180-min solar irradiation, respectively. Moreover, six over a total of eleven transformation products formed during UV photocatalysis were ascribed to the roles of reactive holes (h+), all which were detected and identified by high-resolution liquid chromatography-mass spectrometry (LC-MS). Finally, the pathways of MNZ degradation over Ag-ZnO/GP composite were proposed.

A Simplified Kinetic Modeling of CO2 Absorption into Water and Monoethanolamine Solution in Hollow-Fiber Membrane Contactors.

The absorption of CO2 from CO2-N2 gas mixtures using water and monoethanolamine (MEA) solution in polypropylene (PP) hollow-fiber membrane contactors was experimentally and theoretically examined. Gas was flowed through the lumen of the module, whereas the absorbent liquid was passed counter-currently across the shell. Experiments were carried out under various gas- and liquid-phase velocities as well as MEA concentrations. The effect of pressure difference between the gas and liquid phases on the flux of CO2 absorption in the range of 15-85 kPa was also investigated. A simplified mass balance model that considers non-wetting mode as well as adopts the overall mass-transfer coefficient evaluated from absorption experiments was proposed to follow the present physical and chemical absorption processes. This simplified model allowed us to predict the effective length of the fiber for CO2 absorption, which is crucial in selecting and designing membrane contactors for this purpose. Finally, the significance of membrane wetting could be highlighted by this model while using high concentrations of MEA in the chemical absorption process.

Fouling Analysis in One-Stage Ultrafiltration of Precipitation-Treated Bacillus subtilis Fermentation Liquors for Biosurfactant Recovery.

Primary recovery of surfactin from precipitation-pretreated fermentation broths of Bacillus subtilis ATCC 21332 culture by one-stage dead-end and cross-flow ultrafiltration (UF) was studied. Dead-end experiments were first performed to select suitable conditions, including the amount of added ethanol-a micelle-destabilizing solvent (0-70 vol%), type (polyethersulfone, polyacrylonitrile, poly(vinylidene fluoride)) and molecular-weight cut-off (MWCO, 30-100 kDa) of the membrane in the surfactin concentration range of 0.25-1.23 g/L. Then, the cross-flow UF experiments were conducted to check the recovery performance in the ranges of feed surfactin concentration of 1.13-2.67 g/L, flow velocity of 0.025-0.05 m/s, and transmembrane pressure of 40-100 kPa. The Hermia model was also used to clarify membrane fouling mechanisms. Finally, three cleaning agents and two in situ cleaning ways (flush and back-flush) were selected to regain the permeate flux. As for the primary recovery of surfactin from the permeate in cross-flow UF, a polyethersulfone membrane with 100-kDa MWCO was suggested, and the NaOH solution at pH 11 was used for membrane flushing.

Efficient removal of antibiotic oxytetracycline from water using optimized montmorillonite-supported zero-valent iron nanocomposites.

In this study, montmorillonite-supported nanoscaled zero-valent iron (Mt-nZVI) composites were fabricated using a facile liquid-phase reduction method to avoid serious agglomeration of nZVI particles in suspensions due to magnetic effect. The morphology, crystal structure, functional groups, and magnetic properties of as-prepared composites were explored using scanning and transmission electron microscope, X-ray diffractometer, Fourier transform infrared spectroscope, X-ray photoelectron spectroscope, zeta potential analyzer, and superconducting quantum interference device. The fabricated composites were then applied to remove antibiotic oxytetracycline from water. The optimal weight ratio of the Mt particles (mean size, 25 µm) to the nZVI particles (size, 60-100 nm) was first determined to be 2:1 (simply denoted as 2Mt-nZVI). Experimental results showed that 99% of 100 mg/L oxytetracycline at pH 5.0 was removed using 0.6 g/L of the 2Mt-nZVI composite and the mineralization reached 70% after 20 min of reaction. Finally, the transformation products and intermediates were detected and identified by a high-resolution liquid chromatography mass spectrometry (LC-MS) and the pathways were proposed during the degradation of oxytetracycline over the 2Mt-nZVI composite.

Removal of metronidazole and amoxicillin mixtures by UV/TiO2 photocatalysis: an insight into degradation pathways and performance improvement.

The degradation efficiencies and pathways of metronidazole (MNZ) and amoxicillin (AMX) in binary mixtures by UV/TiO2 photocatalysis were studied. The presence of AMX significantly decreased the degradation of MNZ, whereas the existence of MNZ slightly reduced the degradation of AMX. This is basically due to the difference in attack ability of oxidizing agents present during TiO2 photocatalysis. All oxidizing agents (hydroxyl radicals, superoxide radicals, and holes) could attack AMX molecules, but hydroxyl radicals showed insignificant attack ability in MNZ degradation. In TiO2 photocatalysis of binary mixture, six transformation products were recognized by a high-resolution LC-QTof/MS. Because of competitive effect, only one product was sourced from MNZ degradation and four others were formed due to AMX degradation. The remaining one was a new product of the side reaction. This work indicated that the molecular structure of AMX determined its preferred degradation in a mixture. It not only affected the removal of antibiotics but also figured out the appearance of transformation products. In contrast to single systems, the extent of degradation reduced for each antibiotic in the presence of the second antibiotic was related to the availability of degradation pathways of each antibiotic. Moreover, suitable pH programming was applied to enhance the mineralization of the mixtures.

Removal of metronidazole by TiO2 and ZnO photocatalysis: a comprehensive comparison of process optimization and transformation products.

The photodegradation of antibiotic metronidazole (MNZ) was systematically studied and compared by using aqueous suspensions of TiO2 and ZnO catalysts under 100-W UV irradiation. The degradation conditions were optimized using the central composite design and response surface methodology. The optimal photodegradation conditions obtained were at pH 6.0 with 1.5 g L-1 of TiO2 (86.10% removal for 50 mg L-1 MNZ) and at pH 9.5 with 0.5 g L-1 of ZnO (60.32% removal for 30 mg L-1 MNZ) after 60-min irradiation at 20 °C. The degradation efficiency in the presence of TiO2 was higher than that of ZnO. The participation of active species such as hydroxyl radicals (OH·), holes (h+), and superoxide radicals (O2-·) during MNZ photodegradation over TiO2 and ZnO catalysts was also examined. Experimental results showed that MNZ oxidation was mainly driven by the presence of holes and superoxide radicals. Totally, 10 major intermediates were detected in UV/TiO2 and UV/ZnO photocatalysis of MNZ using LC-QTof/MS system, in which 5 same intermediates were found. The remaining different intermediates led to the variations of degradation pathways of both processes. Moreover, some bigger transformation products than the parent MNZ were detected.