XPS valence band observable light-responsive system for photocatalytic acid Red114 dye decomposition using a ZnO-Cu2O heterojunction.

ZnO-Cu2O composites were made as photocatalysts in a range of different amounts using an easy, cheap, and environment-friendly coprecipitation method due to their superior visible light activity to remove pollutants from the surrounding atmosphere. X-ray diffraction and Fourier transform infrared spectroscopy (FT-IR) have demonstrated that ZnO-Cu2O catalysts are made of highly pure hexagonal ZnO and cubic Cu2O. X-ray photoelectron spectroscopy has confirmed that there is a substantial interaction between the two phases of the resultant catalyst. The optical characterizations of the synthesized ZnO-Cu2O composite were done via UV-vis reflectance spectroscopy. Due to the doping on ZnO, the absorption range of the ZnO-Cu2O catalyst is shifted from the ultraviolet to the visible region due to diffuse reflection. The degradation efficiency is affected by the Ratio of ZnO: Cu2O and ZnO-Cu2O composite with a proportion of 90:10 exhibited the most prominent photocatalytic activity on Acid Red 114, with a pseudo-first-order rate constant of 0.05032 min-1 that was 6 and 11 times greater than those of ZnO and Cu2O, respectively. The maximum degradation efficiency is 97 %. The enhanced photocatalytic activity of the composite is caused by the synergistic interaction of ZnO and Cu2O, which improves visible light absorption by lowering band gap energy and decreasing the rate at which the electron-hole pairs recombine. The scavenging experiment confirmed that hydroxyl radical was the dominant species for the photodegradation of Acid Red 114. Notably, the recycling test demonstrated the ZnO-Cu2O photocatalyst was highly stable and recyclable. These results suggest that the ZnO-Cu2O mix might be able to clean up environmental pollutants when it meets visible light.

Ophiorrhiza mungos-Mediated Silver Nanoparticles as Effective and Reusable Adsorbents for the Removal of Methylene Blue from Water.

Green synthesis of silver nanoparticles (AgNPs) using a plant extract has attracted significant attention in recent years. It is found as an alternative for other physicochemical approaches because of its simplicity, low cost, and eco-friendly rapid steps. In the present study, Ophiorrhiza mungos (Om)-mediated AgNPs have been shown to be effective bioadsorbents for methylene blue (MB) dye removal (88.1 ± 1.74%) just after 1 h at room temperature in the dark from an aqueous medium for the first time. Langmuir and Freundlich isotherms fit the experimental results having the correlation coefficient constants R2 = 0.9956 and R2 = 0.9838, respectively. From the Langmuir fittings, the maximum adsorption capacity and adsorption intensity were found to be 80.451 mg/g and 0.041, respectively, indicating the excellent performance and spontaneity of the process. Taking both models under consideration, interestingly, our findings indicated a fairly cooperative multilayer adsorption that might have been governed by chemisorption and physisorption, whereas the adsorption kinetics followed the pseudo-second-order kinetics mechanism. The positive and low values of enthalpy (ΔH0 = 4.91 kJ/mol) confirmed that adsorption is endothermic and physical in nature; however, the negative free energy and positive entropy value (ΔS0 = 53.69 J/mol K) suggested that the adsorption is spontaneous. The biosynthesized adsorbent was successfully reused up to the fifth cycle. A proposed reaction mechanism for the adsorption process of MB dye onto Om-AgNPs is suggested. The present study may offer a novel finding such as an effective and sustainable approach for the removal of MB dye from water using biosynthesized Om-AgNPs as reusable adsorbents at a comparatively faster rate at a low dose for industrial applications.

Source-specific geochemical and health risk assessment of anthropogenically induced metals in a tropical urban waterway.

Thorough deliberation is necessary to safeguard the tropical urban streams near the shoreline from human interference, as it is becoming a notable environmental danger. Consequently, an in-depth study was carried out on a significant urban waterway located on the southern seashore of Bangladesh, which is positioned in the Bengal delta, renowned as the largest delta in the globe. The current investigation assesses the potential health hazards associated with trace metals (Hg, Cu, As, Pb, Ni, Zn, Cd, Cr, Fe, and Mn) and uses chemometric analysis to determine where they originate. Likewise geochemical methods are used to analyze the levels of trace metal enrichment and pollution in the sediments of the river. Almost all of the elements' mean concentrations were observed to be within the standard limits. The findings not only demonstrate the extent of trace metal contamination but also the health threats that it poses to the public (male, female, and children) by polluting the sediment. For all age groups of people, the hazard index was <1, suggesting there was no non-carcinogenic threat. Regardless of age and sex, exposure occurred in descending order: ingestion > dermal > inhalation. Total carcinogenic risk (TCR) values for males, females, and children were 1.45E-05, 1.56E-05, and 1.34E-04, respectively, recommending that children are at greater vulnerability than adults. The geochemical approach and chemometric analysis corroborate the human-induced impact of trace metal loading in the sediment of the waterway, which is predominantly caused by the oil industry, domestic garbage, and untreated waste discharge.

Comparison of the Effect of Kaolin and Bentonite Clay (Raw, Acid-Treated, and Metal-Impregnated) on the Pyrolysis of Waste Tire.

This study investigates the effectiveness of kaolin and bentonite catalysts in improving liquid hydrocarbon yields during the pyrolysis of waste tires. Raw clay, nitric acid-treated clay, and mono- or bimetal-impregnated clay were used as catalysts in the pyrolysis of waste tire. Acid-treated kaolin produced a higher yield of liquid hydrocarbons (43.24-47%) compared to acid-treated bentonite (35.34-41.85%). This improvement in the liquid yield can be attributed to the higher specific surface area and pore diameter of the acid-treated clay in comparison to raw kaolin (39.48%) and raw bentonite (31.62%). Moreover, the use of metal-impregnated catalysts, such as Fe/kaolin and Ni/Fe/kaolin, resulted in higher liquid yields (47%) compared to the 3 M HNO3-treated kaolin catalyst (43.24%). Gas chromatography-mass spectrometry (GC-MS) analysis confirmed the presence of limonene, a crucial ingredient for commercial perfume production, in the liquid products. The calorific values of oil obtained through kaolin and bentonite catalysis were measured at 13,922 and 10,174 kcal/kg, respectively, further highlighting the potential of these catalysts in waste tire valorization.

Waste newspaper driven activated carbon to remove polycyclic aromatic hydrocarbon from wastewater.

In this study, a carbon-based adsorbent was developed from waste newspaper through pyrolysis at 800 °C to evaluate the removal efficiency of polycyclic aromatic hydrocarbons (Benzo[ghi]perylene (BghiP) and Indeno [1,2,3-cd] pyrene (IP)) from wastewater. The surface area of the developed adsorbent was estimated at 509.247m2g-1 which allowed the adsorption of the PAHs from wastewater. The maximum adsorption capacity was estimated at 138.436 µg g-1 and 228.705 µg g-1 for BghiP and IP, respectively and the highest removal efficiency was observed at pH 2. Around 91% removal efficiency was observed at pH 7 for both pollutants. Experimental adsorption data were fit for pseudo-second-order kinetics and Langmuir isotherm models, which demonstrate electrostatic interaction, monolayered deposition, hydrogen bonding, and π-π interaction between adsorbate and adsorbent which play a significant role in adsorption. The regeneration study described that the developed adsorbent could be able to intake 52.75% BghiP and 48.073% IP until the 8th and 6th cycles, respectively. The removal efficiency of the adsorbent in the real sample was also evaluated. This study will provide a method to convert waste material into adsorbent and will remove PAHs from wastewater as a function of pollutant mitigation and waste management.

Calcined chicken eggshell-derived biomimetic nano-hydroxyapatite as a local drug-delivery aid for doxycycline hyclate: characterization, bio-activity, cytotoxicity, antibacterial activity and in vitro release study.

The integration of bioactive substances with antibiotics has been extensively pursued for the treatment of osteomyelitis. These materials, also known as biomaterials, can serve both as bone replacements and targeted drug delivery systems for antibiotics. In this study, biomimetic nano-hydroxyapatite (nHAp) was synthesized via the coprecipitation technique where waste chicken eggshell (WCE) was employed as the source of Ca. Heat treatment was performed at four different temperatures (100 °C, 300 °C, 600 °C and 900 °C). Subsequently, the samples were characterized using XRD, FTIR spectroscopy, Raman spectroscopy, FESEM, EDX, XPS, DLS hydrodynamic size and zeta potential analysis. Also, their biomedical effectiveness was evaluated in terms of cytotoxicity, hemolysis, antibacterial performance, and bioactivity. Doxycycline hyclate (DOXh) was loaded in the synthesized nHAp samples, and subsequently its in vitro release was studied under stirring in simulated body fluid (SBF). The DOXh release kinetics was evaluated, and it was found that the first-order model was the best fitted kinetic model describing the release of DOXh from the nHAp samples, except for nHAp100, which was best described by the Korsmeyer-Peppas model. The nHAp synthesized utilizing WCE showed excellent potential for biomedical application and can be used as a drug delivery agent for antibiotics, such as DOXh.

Sediment-bound hazardous trace metals(oid) in south-eastern drainage system of Bangladesh: First assessment on human health.

Despite the beneficial aspect of a natural drainage system, increasing human-induced activities, which include urbanization and growth in industrialization, degrade the ecosystem in terms of trace metal contamination. In response, given the great importance of the south-eastern drainage system in Bangladesh, a detailed evaluation of the human health risk as well as the potential ecological risk of trace metals (Be, Cd, Co, Cr, Cu, Hg, Ni, Pb, Se, V, Zn, and As) in Karnaphuli riverbed sediment was conducted. Mean levels of the elements in mg/kg were As (5.62 ± 1.47); Se (0.84 ± 0.61); Hg (0.37 ± 0.23); Be (1.17 ± 0.49); Pb (15.62 ± 8.42); Cd (0.24 ± 0.33); Co (11.59 ± 4.49); Cr (112.75 ± 40.09); Cu (192.67 ± 49.71); V (27.49 ± 10.95); Zn (366.83 ± 62.82); Ni (75.83 ± 25.87). Pollution indicators, specifically contamination factor (CF), pollution load index (PLI), degree of contamination (Cd), enrichment factor (EF), geo-accumulation index (Igeo), and potential ecological risk index (RI), were computed to assess sediment quality. For the first observation of health risk, chronic daily intake (CDI), hazard quotient (HQ), hazard index (HI), carcinogenic risk (CR) and total carcinogenic risk (TCR) indices were calculated. According to the results, CDI values through the ingestion route of both the adult and child groups were organized in the following descending mode respectively: Zn > Cu > Cr > Ni > V > Pb > Co > As > Se > Be > Cd > Hg. The non-carcinogenic risks were generally low for all routes of exposure, except HQingestion was slightly higher for both adults and children. The calculated hazard index (HI) was, nevertheless, within the permitted range (HI < 1). Similarly, none of the metals exhibited any carcinogenic risks, as all CR values were within the 10-4-10-6 range. The need for authoritative efforts and water policy for the sake of the surrounding ecosystem and human health in the vicinity of the examined watershed is strongly felt as an outcome of this study. The purpose of this study is to protect public health by identifying trace metal sources and reducing industrial and domestic discharge into this natural drainage system.

A combined first principles and experimental approach to Bi2WO6.

Here we synthesized Bi2WO6 (BWO) using both solid-state reaction (SBWO) and hydrothermal (HBWO-U and HBWO-S) methods. The orthorhombic Pca21 phase purity in all samples is confirmed from Rietveld refinement of X-ray diffraction data, Raman spectroscopy, and Fourier transform infrared spectroscopy. The HBWO-U and HBWO-S morphology revealed rectangular, spherical, and rod-like features with an average particle size of 55 nm in field emission scanning electron micrographs. A high-resolution transmission electron micrograph showed spherical-shaped particles in the HBWO-U sample with an average diameter of ∼10 nm. The diffuse reflectance-derived indirect electronic band gaps lie within the 2.79-3.23 eV range. The BWO electronic structure is successfully modeled by Hubbard interaction Ud and Up corrected Perdew-Burke-Ernzerhof generalized gradient approximation GGA-PBE+Ud+Up with van der Waals (vdW) force in effect. The optimized (Ud, Up) values are further justified by tuning the Hartree-Fock (HF) exact-exchange mixing parameter αHF from 25% in Heyd-Scuseria-Ernzerhof (HSE06) to 20% in the PBE-HF20% functional. Moreover, no inconsistencies were seen in the GGA-PBE+Ud+Up+vdW simulated crystallographic parameters, and the elastic tensor, phonon, and linear optical properties. Overall, the computationally cheap GGA-PBE+Ud+Up with vdW force may have successfully probed the physical properties of BWO.