Ceria-doped SnO2 nanocubes for solar light–driven photocatalytic hydrogen production

Environmental Science and Pollution Research - The photocatalytic generation of hydrogen via solar energy using metal oxide semiconductor catalysts is a clean and renewable process which has the...     

Synthesis of γ-Fe2O3/La/Bi2WO6 composites for enhanced visible light-driven photocatalytic degradation of tetracycline hydrochloride

Environmental Science and Pollution Research - γ-Fe2O3/La/Bi2WO6 heterojunction composites have been successfully synthesized by simple and convenient hydrothermal method. The photocatalytic...     

Ag/ZnO hollow sphere composites: reusable photocatalyst for photocatalytic degradation of 17α-ethinylestradiol

Characterizations of Ag/ZnO hollow sphere by scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectra, and UV–vis absorption spectra have been made after its synthesis. The results showed that the composite was hollow structure with diameters of about 1–4 μm. The samples synthesized were tested and identified as silver doped ZnO, which have extended and boosted the spectral absorption. The photocatalytic activity of Ag/ZnO hollow spheres was assessed using 17α-ethinylestradiol aqueous solution under UV irradiation. It has been observed that the 17α-ethinylestradiol absorption efficiency and degradation rate is higher for Ag/ZnO hollow spheres. As reusable photocatalysts, Ag/ZnO hollow spheres which could be easily separated from a suspension will facilitate their application in wastewater treatment with enhanced photostability.     

Solar light–driven photocatalytic degradation and mineralization of beta blockers propranolol and atenolol by carbon dot/TiO2 composite

Herein improved solar light–driven photocatalytic degradation and mineralization of two emerging pollutants as well as recalcitrant beta blockers propranolol (PR) and atenolol (AT) have been demonstrated by metal-free carbon dot/TiO₂ (CDT) composite. Hydrothermally synthesized TiO₂ has been decorated with electrochemically synthesized carbon dots (CDs) and was well characterized by various analytical techniques viz. XRD, FTIR, Raman, XPS, UV–visible DRS, FESEM, and TEM. The optimized CDT composite, 2CDT (2 mL carbon dot/TiO₂), showed?~?3.45- and?~?1.75-fold enhancement in the photodegradation rate as compared to pristine TiO₂ for PR and AT respectively in 1 hour of irradiation along with complete degradation of PR and AT after 3 hours of irradiation. 2CDT exhibited 76% and 80% mineralization of PR and AT in contrast with 62% and 47% observed by pristine TiO₂. Further, the major reaction intermediates formed after degradation have been identified by HPLC/MS analysis, confirming more than 99% reduction of the parent compound for both PR and AT. Reusability of the optimized catalyst also showed successful degradation up to 3 cycles, showing reduction abilities of 97%, 95%, and 94% for 1st, 2nd, and 3rd cycle respectively. The enhanced degradation and mineralization efficiency of the 2CDT composite could be attributed to the excellent photosensitizer and electron reservoir properties of the CD along with upconverted photoluminescence behavior. The present study unlocks the possibility of using metal-free, facile CDT composite for effective degradation and mineralization of widely used beta blockers and other pharmaceuticals.

     

Evaluation of chlordimeform and degradation products for mutagenic and DNA‐damaging activity in salmonella typhimurium and escherichia coli

Abstract

The mutagenic activity of chlordimeform and two of its breakdown products, 4‐chloro‐o‐toludine and 4‐chloro‐N‐formyl‐o‐toluidine were determined with five histidine dependent strains of Salmonella typhimurium (TA1535, TA1537, TA1538, TA98, TA100) and five tryptophan dependent strains of E. coli WP₂. (WP₂, WP₂uvrA, WP67, CM611, CM571) with and without rat liver microsomal enzymes. 4‐chloro‐o‐toluidine increased the number of the reversions of the S. typhimurium strain TA1535 more than two fold over spontaneous at the concentration of 400 μg/plate.

The results of the DNA repair tests in the Salmonella TA1538/TA1978 and E. coli multirepair deficient systems showed that both breakdown products were active in inducing damage not repaired in at least one repair deficient strain while chlordimeform itself was inactive.     

Preparation,characterization, and photocatalytic activity evaluation of Fe–N-codoped TiO2/fly ash cenospheres floating photocatalyst

Nitrogen-doped titanium dioxide (TiO₂) and Fe–N-codoped TiO₂ layers on fly ash cenospheres (FAC) as floating photocatalyst were successfully prepared through sol–gel method. Photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), ultraviolet (UV)–Vis diffuse reflectance spectroscopy (DRS), and nitrogen adsorption analyses for Brunauer–Emmett–Teller (BET) specific surface area. Photocatalytic efficiency of the prepared catalyst was evaluated through using the decomposition of Rhodamine B (RhB) as a model compound under visible light irradiation. Photocatalytic activity and kinetics of catalyst under visible light were detected in details from different Fe/Ti mole ratios by detecting photodegradation of RhB. Experimental results show that when the calcination temperature was 550 °C, the dosage of FAC was 3.0 g, and the mole ratio of Fe/Ti was 0.71 %; the synthesized Fe–N-TiO₂/FAC photocatalyst presented as anatase phase and that N and Fe ions were doped into TiO₂ lattice. The material’s specific surface area was 34.027 m²/g, and UV–Vis diffuse reflectance spectroscopy shows that the edge of the photon absorption has been red shifted up to 400–500 nm. Fe–N-codoped titanium dioxide on FAC had excellent photocatalytic activity during the process of photodegradation of RhB under visible light irradiation.

     

Pyridinic N–reduced graphene oxide and ZnO composite synergistically enhance photocatalytic performance

Environmental Science and Pollution Research - This paper reports the synthesis of nitrogen-doped reduced graphene oxide (N-rGO)/zinc oxide (ZnO) composite photocatalysts by one-step hydrothermal...     

Novel PVA/chitosan composite membrane modified using bio-fabricated α-MnO2 nanoparticles for photocatalytic degradation of cationic dyes

Environmental Science and Pollution Research - By integrating the benefits of poly vinyl alcohol (PVA) and chitosan (CS) with α-MnO2 nanoparticles (MNPs), a novel type of nano-polymer...     

Comparative photocatalytic dye and drug degradation study using efficient visible light–induced silver phosphate nanoparticles

Environmental Science and Pollution Research - The industrialization, growing population, and human activities (e.g., liquid waste of households, industrial units, and agricultural lands) are the...     

Influence of the presence of ruthenium on the activity and stability of Co–Mg–Al-based catalysts in CO2 reforming of methane for syngas production

Environmental Science and Pollution Research - Hydrogen production by methane dry reforming is an important yet challenging process. A performing catalyst will favor the thermodynamic equilibrium...     

Hydrogen peroxide–assisted photocatalytic dye degradation over reduced graphene oxide integrated ZnCr2O4 nanoparticles

Environmental Science and Pollution Research - Zinc chromite nanoparticles (NPs) and zinc chromite–reduced graphene oxide (ZnCr2O4-rGO) nanocomposite have been synthesized by the combined...     

Adsorptive removal and photocatalytic decomposition of sulfamethazine in secondary effluent using TiO2–zeolite composites

We investigated the adsorption and decomposition of sulfamethazine (SMT), which is used as a synthetic antibacterial agent and discharged into environmental water, using high-silica Y-type zeolite (HSZ-385), titanium dioxide (TiO₂), and TiO₂–zeolite composites. By using ultrapure water and secondary effluent as solvents, we prepared SMT solutions (10 μg/L and 10 mg/L) and used them for adsorption and photocatalytic decomposition experiments. When HSZ-385 was used as an adsorbent, rapid adsorption of SMT in the secondary effluent was confirmed, and the adsorption reached equilibrium within 10 min. The photocatalytic decomposition rate using TiO₂ in the secondary effluent was lower than that in ultrapure water, and we clarified the inhibitory effect of ions and organic matter contained in the secondary effluent on the reaction. We synthesized TiO₂–zeolite composites and applied them to the removal of SMT. During the treatment of 10 μg/L SMT in the secondary effluent using the composites, 76 % and more than 99 % of the SMT were decomposed within 2 and 4 h by photocatalysis. The SMT was selectively adsorbed onto high-silica Y-type zeolite in the composites. Resultantly, the inhibitory effect of the coexisting materials was reduced, and the composites could remove SMT more effectively compared with TiO₂ alone in the secondary effluent.     

Production and characterization of novel thermo- and organic solvent–stable keratinase and aminopeptidase from Pseudomonas aeruginosa 4–3 for effective poultry feather degradation

Environmental Science and Pollution Research - Feather biodegradation is an important premise for efficient resource development and utilization, in which keratinase plays an important role....     

Synthesis and characterisation of transition metal sulphide-loaded fly ash–based mesoporous EU-12 photocatalysts for degradation of rhodamine B

Transition metal sulphide-loaded fly ash–based EU-12 photocatalysts were synthesized by sono-hydrothermal method followed by ion exchange. The composites were characterized by XRD, FESEM, DSC-TGA, Raman spectroscopy, and BET surface area analysis. The XRD results imply 76.39% crystallinity of EU-12 and morphological studies by FESEM, and TEM revealed the shape and size of EU-12, i.e. rod-shaped with size ranging from 5 to 200 nm. Band gap of all synthesized photocatalysts were found to be?≤?3.44 eV. The photoactivities of the photocatalysts were examined by degrading rhodamine B (RhB). The results indicated that metal sulphide/EU-12 composite had the strong photoactivity under visible light compared to dark environment. Furthermore, the efficiency of photocatalysts was determined in terms of degradation efficiency towards RhB which was found to be maximum of 98.62% for 0.2 M CdS/EU-12 at 2 gL^?1 of catalyst dosage and 10 ppm of dye concentration within 3 h under visible light source of 200 W.

     

Magnetic photocatalysts from δ-FeOOH and TiO2 and application in reactions for degradation of methylene blue and paracetamol with UV-C and sunlight

Environmental Science and Pollution Research - Water contamination is a common problem, especially considering dyes and drugs disposal. A possible and effective treatment method to remove these...     

Estrogenic effects of dissolved organic matter and its impact on the activity of 17β-estradiol

Background and purpose  

The ubiquitous dissolved organic matter (DOM) is actually not inert as we always think, and the hormone-like effects of DOM have been reported. The objective of this study was to investigate the estrogenic effects of DOM and its impact on the activity of the natural estrogen 17β-estradiol (E2).     

Titanium dioxide and graphitic carbon nitride–based nanocomposites and nanofibres for the degradation of organic pollutants in water: a review

Environmental Science and Pollution Research - The paper reviews graphitic carbon nitride–based nanostructured photocatalytic materials and nanofibres for applications in water purification....     

Photocatalytic degradation of acetaminophen and caffeine using magnetite–hematite combined nanoparticles: kinetics and mechanisms

Environmental Science and Pollution Research - The increased use of pharmaceutical and personal care products (PPCPs) has contributed to the contamination of water systems and put pressure on the...     

Application of activated M/ZnO (M = Mn,Co, Ni,Cu, Ag) in photocatalytic degradation of diazo textile coloring dye

Activated ZnO powder has been prepared by procedures involving first its dissolution in nitric acid, then simultaneous treatment by adding NH₄OH and CO₂ bubbling leading to precipitation as Zn(OH)CO₃ (ZH) and further thermal decomposition of ZH at 400 °C. The gas evolution leads to formation of pores and increase in the specific surface area. Chemically activated M/ZnO powders doped with Mn, Co, Ni, Cu, and Ag have been obtained by the impregnation method. The samples have been characterized by ultraviolet-visible (UV-Vis) spectroscopy, diffuse reflectance (DR) UV-Vis, X-ray diffraction (XRD), single point Brunauer–Emmet–Teller (BET), scanning electron microscope (SEM), and X-ray photoelectron spectroscopy (XPS) methods. The experiments have shown that metal-doped activated ZnO powders possess higher photocatalytic activities in oxidative discoloration of model contaminant textile coloring dye Reactive Black 5 in slurry reactor compared to that of the pure ZnO. The XRD and XPS data have shown the presence of defects, nonstoichiometricity implying the formation of solid solutions. Copper-doped (1.5 wt%) activated ZnO (Cu²⁺ replaces Zn²⁺) is outstanding in its photocatalytic performance in discoloration of the dye due to the higher specific surface area and improved charge carrier separation.