4-Nitrophenol reduction and antibacterial activity of Ag-doped TiO2 photocatalysts.

Water contamination by organic pollutants is a serious environmental problem. 4-Nitrophenol (4-NP) is a potentially harmful chemical, which is commonly present in industrial effluents and can severely damage human health. Photocatalytic reduction of hazardous 4-NP by nano-sized materials to produce 4-aminophenol (4-AP), which is a commercially valuable product, is a promising alternative as the process is framed within the circular economy. In this context, Ag-doped TiO2 (AT) catalysts were synthesized by liquid impregnation and reduction techniques, and their structure, morphology, elemental composition, textural, and light absorption properties were evaluated by XRD, Raman spectroscopy, SEM, TEM, EDS, BET, and DRS spectroscopy. AT catalysts exhibited an enhanced photocatalytic reduction of 4-NP into 4-aminophenol (4-AP) in the presence of NaBH4. Among the tested catalysts, AT21 prepared by a simple aqueous reduction method showed the highest activity reaching about 98% 4-NP reduction within 10 min. Antibacterial tests of these catalysts against Bacillus subtilis, Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa revealed that AT21 also exhibited the lowest minimum inhibitory concentration, suggesting that it has the strongest antibacterial activity. These findings suggest that AT21 catalyst with improved catalytic and antibacterial properties can potentially be utilized for the remediation of 4-NP-contaminated water environment.

Uncovering the Role of Surface-Attached Ag Nanoparticles in Photodegradation Improvement of Rhodamine B by ZnO-Ag Nanorods.

ZnO nanorods decorated with metal nanoparticles have sparked considerable interest in recent years thanks to their suitability for a wide range of applications, such as photocatalysis, photovoltaics, antibacterial activity, and sensing devices. In this study, we prepared and investigated the improved solar-light-assisted photocatalytic activity of ZnO nanorods (NRs) decorated with Ag nanoparticles (NPs) using a conventional rhodamine B (RB) dye as a model water pollutant. We showed that the presence of Ag NPs on the surface of ZnO NRs significantly increases the degradation rate of RB dye (~0.2432 min-1) when compared to bare ZnO NRs (~0.0431 min-1). The improved photocatalytic activity of ZnO-Ag was further experimentally tested using radical scavengers. The obtained results reveal that ˙OH and ˙O2- radicals are main active species involved in the RB dye photodegradation by ZnO-Ag NRs. It was concluded that efficient charge separation plays a major role in photocatalytic activity improvement.

Degradation of 4-Tert-Butylphenol in Water Using Mono-Doped (M1: Mo, W) and Co-Doped (M2-M1: Cu, Co, Zn) Titania Catalysts.

Mono-doped (Mo-TiO2 and W-TiO2) and co-doped TiO2 (Co-Mo-TiO2, Co-W-TiO2, Cu-Mo-TiO2, Cu-W-TiO2, Zn-Mo-TiO2, and Zn-W-TiO2) catalysts were synthesized by simple impregnation methods and tested for the photocatalytic degradation of 4-tert-butylphenol in water under UV (365 nm) light irradiation. The catalysts were characterized with various analytical methods. X-ray diffraction (XRD), Raman, Diffuse reflectance (DR) spectroscopies, Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), and Energy dispersive spectroscopy (EDS) were applied to investigate the structure, optical properties, morphology, and elemental composition of the prepared catalysts. The XRD patterns revealed the presence of peaks corresponding to the WO3 in W-TiO2, Co-W-TiO2, Cu-W-TiO2, and Zn-W-TiO2. The co-doping of Cu and Mo to the TiO2 lattice was evidenced by the shift of XRD planes towards higher 2θ values, confirming the lattice distortion. Elemental mapping images confirmed the successful impregnation and uniform distribution of metal particles on the TiO2 surface. Compared to undoped TiO2, Mo-TiO2 and W-TiO2 exhibited a lower energy gap. Further incorporation of Mo-TiO2 with Co or Cu introduced slight changes in energy gap and light absorption characteristics, particularly visible light absorption. In addition, photoluminescence (PL) showed that Cu-Mo-TiO2 has a weaker PL intensity than undoped TiO2. Thus, Cu-Mo-TiO2 showed better catalytic activity than pure TiO2, achieving complete degradation of 4-tert-butylphenol under UV light irradiation after 60 min. The application of Cu-Mo-TiO2 under solar light conditions was also tested, and 70% of 4-tert-butylphenol degradation was achieved within 150 min.

Anaerobic Membrane Bioreactors for Municipal Wastewater Treatment: A Literature Review.

Currently, there is growing scientific interest in the development of more economic, efficient and environmentally friendly municipal wastewater treatment technologies. Laboratory and pilot-scale surveys have revealed that the anaerobic membrane bioreactor (AnMBR) is a promising alternative for municipal wastewater treatment. Anaerobic membrane bioreactor technology combines the advantages of anaerobic processes and membrane technology. Membranes retain colloidal and suspended solids and provide complete solid-liquid separation. The slow-growing anaerobic microorganisms in the bioreactor degrade the soluble organic matter, producing biogas. The low amount of produced sludge and the production of biogas makes AnMBRs favorable over conventional biological treatment technologies. However, the AnMBR is not yet fully mature and challenging issues remain. This work focuses on fundamental aspects of AnMBRs in the treatment of municipal wastewater. The important parameters for AnMBR operation, such as pH, temperature, alkalinity, volatile fatty acids, organic loading rate, hydraulic retention time and solids retention time, are discussed. Moreover, through a comprehensive literature survey of recent applications from 2009 to 2021, the current state of AnMBR technology is assessed and its limitations are highlighted. Finally, the need for further laboratory, pilot- and full-scale research is addressed.

Photochemical mineralization of amoxicillin medicinal product by means of UV, hydrogen peroxide, titanium dioxide and iron.

In the present study, the photochemical degradation of amoxicillin and total organic carbon (TOC) removal in pharmaceutical aqueous solutions was studied using UV irradiation, titanium dioxide, hydrogen peroxide and iron in a batch photoreactor operated for 120-150 min. The effect of the initial concentrations of the target compound, hydrogen peroxide and ferric ions and of their combination was examined. It was found that under direct UV photolysis, considerable TOC removals were obtained only when the initial concentration of amoxicillin (AM) was below 100 mg/L. For initial concentration of AM 250 mg/L, the TOC removals achieved were of no practical use (below 5%). The TOC removals achieved in the presence of TiO2 were lower than 20% in all cases. In the presence of hydrogen peroxide in the range of 12.2-146.9 mmol/L and initial AM concentration 250 mg/L, for increasing H2O2 concentrations higher TOC removals were achieved up to the concentration of 73.4 mmol/L H2O2. The presence of even very small amounts of Fe(III) in the solution resulted in significantly increased TOC removals; 2.2 times higher than without Fe(III) after 120 min. Fe(III) presence accelerated dramatically the process during the first 60 min. The origin of Fe(III) ions was not important since practically the same results were obtained whether FeCl3 or Fe(NO3)3 was used as source of ferric ions. Adjusting the initial concentrations of AM, Fe(III) and H2O2, TOC removals above 90% were achieved.

Effective photochemical treatment of a municipal solid waste landfill leachate.

This work aimed at studying the photochemical treatment of a landfill leachate using ultraviolet light, hydrogen peroxide, and ferrous or ferric ions, in a batch recycle photoreactor. The effect of inorganic carbon presence, pH, initial H2O2 amount (0-9990 mg L-1) as well as Fe(II) (200-600 ppm) and Fe(III) (300-700 ppm) concentrations on the total carbon removal and color change was studied. Prior to the photochemical treatment, a pretreatment process was applied; inorganic nitrogen and inorganic carbon were removed by means of air stripping and initial pH regulation, respectively. The leachate sent subsequently for photochemical treatment was free of inorganic carbon and contained only organic carbon with concentration 1200±100 mg L-1 at pH 5.1-5.3. The most favorable concentrations of H2O2 and ferric ions for carbon removal were 6660 mg L-1 and 400 ppm, respectively. Adjusting the initial pH value in the range of 2.2-5.3 had a significant effect on the organic carbon removal. The photo-Fenton-like process was more advantageous than the photo-Fenton one for leachate treatment. By applying the most favorable operating conditions, 88.7% removal of total organic carbon, 100% removal of total inorganic carbon, 96.5% removal of total nitrogen, and 98.2% color removal were achieved.

Clustering analysis of countries using the COVID-19 cases dataset.

There is a worldwide effort of the research community to explore the medical, economic and sociologic impact of the COVID-19 pandemic. Many different disciplines try to find solutions and drive strategies to a great variety of different very crucial problems. The present study presents a novel analysis which results to clustering countries with respect to active cases, active cases per population and active cases per population and per area based on Johns Hopkins epidemiological data. The presented cluster results could be useful to a variety of different policy makers, such as physicians and managers of the health sector, economy/finance experts, politicians and even to sociologists. In addition, our work suggests a new specially designed clustering algorithm adapted to the request for comparison of the various COVID time-series of different countries.

A review of cryogels synthesis, characterization and applications on the removal of heavy metals from aqueous solutions.

The physical and chemical attributes of cryogels, such as the macroporosity, elasticity, water permeability and ease of chemical modification have attracted strong research interest in a variety of areas, such as water purification, catalysis, regenerative medicine, biotechnology, bioremediation and biosensors. Cryogels have shown high removal efficiency and selectivity for heavy metals, nutrients, and toxic dyes from aqueous solutions but there are challenges when scaling up from lab to commercial scale applications. This paper represents an overview of the most recent advances in the use of cryogels for the removal of heavy metals from water and attempts to fill the gap in the literature by deepening the understanding on the mechanisms involved, which strongly depend on the initial monomer composition and post-modification agent precursors used in synthesis. The review also describes the advantages of cryogels over other adsorbents and covers synthesis and characterization methods such as SEM/EDS, TEM, FTIR, zeta potential measurements, porosimetry, swelling and mechanical properties.

Degradation and mineralization of 4-tert-butylphenol in water using Fe-doped TiO2 catalysts.

In the present work, the photocatalytic degradation and mineralization of 4-tert-butylphenol in water was studied using Fe-doped TiO2 nanoparticles under UV light irradiation. Fe-doped TiO2 catalysts (0.5, 1, 2 and 4 wt.%) were prepared using wet impregnation and characterized via SEM/EDS, XRD, XRF and TEM, while their photocatalytic activity and stability was attended via total organic carbon, 4-tert-butyl phenol, acetic acid, formic acid and leached iron concentrations measurements. The effect of H2O2 addition was also examined. The 4% Fe/TiO2 demonstrated the highest photocatalytic efficiency in terms of total organic carbon removal (86%). The application of UV/H2O2 resulted in 31% total organic carbon removal and 100% 4-t-butylphenol conversion, however combining Fe/TiO2 catalysts with H2O2 under UV irradiation did not improve the photocatalytic performance. Increasing the content of iron on the catalyst from 0.5 to 4% considerably decreased the intermediates formed and increased the production of carbon dioxide. The photocatalytic degradation of 4-tert-butylphenol followed pseudo-second order kinetics. Leaching of iron was observed mainly in the case of 4% Fe/TiO2, but it was considered negligible taking into account the iron load on catalysts. The electric energy per order was found in the range of 28-147 kWh/m3/order and increased with increasing the iron content of the catalyst.

Photocatalytic treatment of organic pollutants in a synthetic wastewater using UV light and combinations of TiO2, H2O2 and Fe(III).

In this study, the photocatalytic treatment of an organic wastewater with/without phenolic compounds by means of ultraviolet irradiation, titanium dioxide and hydrogen peroxide was examined in an annular photoreactor. Specifically, the effect of initial total carbon concentration, catalyst loading and H2O2 amount on the removal of total carbon was first examined in the case of a synthetic organic wastewater. The influence of partial carbon substitution by phenol, 2-chlorophenol, 2,4-discholophenol, trichlorophenol, and 4-nitrophenol on total carbon removal and target compounds' conversion was studied keeping constant the initial organic carbon load. It was shown that the process applied was effective in treating the wastewater for initial total carbon 32 mg L-1, 0.5 g L-1 TiO2, and 66.6 mg L-1 H2O2. Applying UV/TiO2 and UV/H2O2, 58% and 53% total carbon removals were achieved, respectively, but combining TiO2 and H2O2 did not result in a better performance in the case of the synthetic wastewater without any phenolic compounds. In contrast, when a phenolic compound was added, the addition of H2O2 was beneficial, eliminating the differences observed from one phenolic compound to another. The total carbon removals observed were lower than the corresponding final conversions of the target phenolic compounds. Finally, the electric energy per order values were calculated and found to range in 52-248 kWh/m3/order, being dependent from the process applied and the phenolic compound present in the wastewater.

Photochemical mineralization of Ibuprofen medicinal product by means of UV, hydrogen peroxide, titanium dioxide and iron.

Pharmaceutical compounds contribute to the emerging pollutants in water and in many cases, they are not efficiently mineralized by conventional treatment methods. At the same time, landfills remain the main final destination of discarded drugs. In the present study, the mineralization of the Ibuprofen medicinal commercial product (Algofren®) in aqueous solutions using UV irradiation, hydrogen peroxide, titanium dioxide and ferric ions was examined. All experiments were conducted in a batch photoreactor operated for 120-150 min. The main target was to select the most effective operating conditions for the mineralization of the solutions treated. Single photolysis or TiO2 photocatalysis were proved inefficient in eliminating the total organic carbon (TOC). By adjusting the initial amounts of Ibuprofen product and hydrogen peroxide, 81% TOC removal was achieved after 120 min. Adding iron in the solution led to a higher mineralization degree, especially during the first 30 min of the process. Iron was shown also to decrease the environmental footprint of the process as expressed via the electric energy per order, EEo.

Catalytic destruction of gaseous ethanol and product formation over CuO/CeO2/Al2O3 catalysts.

In the present work, the catalytic decomposition or oxidation of ethanol over CuO/CeO(2)/γ-alumina catalysts is presented. Ethanol was oxidized in a tubular flow reactor under both oxygen excess and deficit conditions. Various amounts of ceria (0-14 % w/w) were added by wet impregnation to catalysts containing 1 % and 10 % w/w CuO on γ-Al(2)O(3). Ceria addition affected catalyst performance mostly at low CuO loading and the formation of the main reaction products, namely acetaldehyde and carbon dioxide, depended strongly on oxygen concentration. The formation of the rest reaction products (i.e., ethylene and diethylether) depended on both oxygen concentration and amount of ceria on the catalyst used.