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In light of growing environmental concerns over emerging contaminants in aquatic environments, antibiotics in particular, have prompted the development of a new generation of effective sonocatalytic systems. In this study, a new type of nano-laminated material, Ti2SnC MAX phase, is prepared, characterized, and evaluated for the sonocatalytic degradation of oxytetracycline (OTC) antibiotic. A variety of identification analyses, including X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectrometry, Brunauer-Emmett-Teller, and diffuse reflectance spectroscopy, were conducted to determine the physicochemical properties of the synthesized catalyst. By optimizing the operating factors, total degradation of OTC occurs within 120 min with 1 g L-1 catalyst, 10 mg L-1 OTC, at natural pH of 7.1 and 150 W ultrasonic power. The scavenger studies conclude that the singlet oxygen and superoxide ions are the most active species during the sonocatalytic reaction. Based on the obtained data and GC–MS analysis, a possible sonocatalytic mechanism for the OTC degradation in the presence of Ti2SnC is proposed. The catalyst reusability within eight consecutive runs reveals the proper stability of Ti2SnC MAX phase. The results indicate the prospect for MAX phase-based materials to be developed as efficient sonocatalysts in the treatment of antibiotics, suggesting a bright future for the field.

Here, we investigate the band structure, density of states, photocatalytic activity, and heterojunction mechanism of WS2 with CeO2 (CeO2@WS2) as a photoactive heterostructure. In this heterostructure, CeO2′s growth within WS2 layers is achieved through ultrasonicating WS2 and intercalating CeO2′s precursor within the WS2 interlayers, followed by hydrothermal treatment. Through a set of density functional calculations, we demonstrate that CeO2 and WS2 form an interface through a covalent bonding that can be highly stable. The electrochemical impedance spectroscopy (EIS) found that the CeO2@WS2 heterostructure exhibits a remarkably higher conductivity (22.23 mS cm−2) compared to either WS2 and CeO2, assignable to the interface in CeO2@WS2. Furthermore, in a physically mixed CeO2-WS2 where the interaction between particles is noncovalent, the resistance was significantly higher (0.67 mS cm−2), confirming that the heterostructure in the interface is covalently bonded. In addition, Mott-Schottky and the bandgap measurements through Tauc plots demonstrate that the heterojunction in CeO2 and WS2 is type II. Eventually, the CeO2@WS2 heterostructure indicated 446.7 µmol g −1 CO2 generation from photocatalytic oxidation of a volatile organic compound (VOC), formic acid, compared to WS2 and CeO2 alone.

Metribuzin is an herbicide that easily contaminates ground and surface water. Herein, La-doped ZnFe layered double hydroxide (LDH) was synthesized for the first time and used for the degradation of metribuzin via ultrasonic (US) assisted peroxydisulfate (PDS) activation. The synthesized LDH had a lamellar structure, an average thickness of 26 nm, and showed mesoporous characteristics, including specific surface area 110.93 m2 g−1, pore volume 0.27 cm3 g−1, and pore diameter 9.67 nm. The degradation efficiency of the US/La-doped ZnFe LDH/PDS process (79.1 %) was much greater than those of the sole processes, and the synergy factor was calculated as 3.73. The impact of the reactive species on the sonocatalytic process was evaluated using different scavengers. After four consecutive cycles, 10.8 % loss occurred in the sonocatalytic activity of the La-doped LDH. Moreover, the efficiency of the US/La-doped LDH/PDS process was studied with respect to the degradation of metribuzin in a wastewater matrix. According to GC–MS analysis, six by-products were detected during the degradation of metribuzin. Our results indicate that the US/La-doped ZnFe LDH/PDS process has great potential for efficient degradation of metribuzin-contaminated water and wastewater.

Supercapacitors and water splitting cells have recently played a key role in offering green energy through converting renewable sources into electricity. Perovskite-type electrocatalysts such as BaTiO3, have been well-known for their ability to efficiently split water and serve as supercapacitors due to their high electrocatalytic activity. In this study, BaTiO3, Al-doped BaTiO3, Ce-doped BaTiO3, and Al-Ce co-doped BaTiO3 nanofibers were fabricated via a two-step hydrothermal method, which were then characterized and compared for their electrocatalytic performance. Based on the obtained results, Al-Ce co-doped BaTiO3 electrode exhibited a high capacitance of 224.18 Fg−1 at a scan rate of 10 mVs−1, high durability during over the 1000 CV cycles and 2000 charge–discharge cycles, proving effective energy storage properties. Additionally, the onset potentials for OER and HER processes were 11 and − 174 mV vs. RHE, respectively, demonstrating the high activity of the Al-Ce co-doped BaTiO3 electrode. Moreover, in overall water splitting, the amount of the overpotential was 0.820 mV at 10 mAcm−2, which confirmed the excellent efficiency of the electrode. Hence, the remarkable electrocatalytic performance of the Al-Ce co-doped BaTiO3 electrode make it a promising candidate for renewable energy technologies owing to its high conductivity and fast charge transfer. [ABSTRACT FROM AUTHOR]

The high-salinity wastewater from the textile industry faces a significant challenge in effectively separating dyes and salts. In this study, a CeZnFe-layered double hydroxide (LDH)-incorporated nanofiltration (LNF) membrane was fabricated using the conventional interfacial polymerization (IP) technique to fractionate dyes and salts within the wastewater. The impact of CeZnFe LDH on various aspects of membrane performance was examined, including water flux, dye removal efficiency, dye/salt separation capability, self-cleaning ability, and membrane integrity. The addition of LDHs resulted in improved membrane surface hydrophilicity, thereby enhancing water flux. The optimized TFN membrane (0.050 wt% LDH in PIP solution) significantly improved pure water flux, exceeding 150%. All TFN membranes exhibited excellent performance in dye and salt fractionation (93% for Congo red, 2.6% for NaCl, and 40.7% for Na2SO4). Also, excellent self-cleaning ability was observed for the optimized membrane, exhibiting a remarkable water flux recovery rate after three operation cycles. Moreover, including CeZnFe LDH in the optimized TFN membrane played a significant role in enhancing membrane integrity. This study provides new inspiration for fabricating self-cleaning loose NF membranes using CeZnFe LDH for effective dye/salt separation.

Layered double hydroxide functionalized biochar and hydrochar composites are environmentally friendly and low-cost adsorbents for the removal of phosphate from aqueous solutions. In the present study, Mg-Al layered double hydroxide functionalized apple wood biochar and hydrochar were prepared and their phosphate adsorption characteristics were examined through batch experiments. Moreover, important factors affecting adsorption including initial phosphorus concentration (25-200 mg/L), contact time (5-120 min), ionic strength (deionized water, and 0.001, 0.01, and 0.1 mol/L KCl), pH (3-10), and adsorbent dosage (1, 2, 3, and 4 g/L) were investigated. Based on the results, the phosphate adsorption by Mg-Al layered double hydroxide modified biochar and hydrochar were comparable with Mg-Al layered double hydroxide and were greater than biochar and hydrochar. As expected, phosphate adsorption was decreased by increasing solution pH and ionic strength. The highest phosphate removal was attained at pH 4, adsorbent dosage of 4 g/L, and in the presence of deionized water as a background solution. Determination of adsorption characteristics of the adsorbents revealed that the phosphate adsorption mechanism involved a combination of electrostatic attraction, interlayer anion exchange, and formation of surface complexes. The Mg-Al layered double hydroxide modified biochar and hydrochar composites as cost-effective and efficient adsorbents suggest alternative biochar- and hydrochar-based composites for the phosphate removal from contaminated waters that could be used as P-fertilizers.

On the basis of recent advances in battery research and technology, we have developed a novel laboratory exercise centered on an organic--inorganic battery using the redox chemistry of the organic molecule anthraquinone-2,7-disulfonic acid disodium salt (AQDS). Although most commercially available batteries are based on inorganic redox couples, the development of batteries based on organic redox active materials has great potential for stationary energy storage. As such, the experiment described in this report exposes students to state-of-the-art battery technology, despite a rather simple experimental protocol. The exercise allows students to acquire hands-on learning and visualize central concepts of the Nernst equation, battery technology and components, half-cell reactions, charging/discharging tests, and performance analysis. Additionally, students are required to operate a range of key electronic instruments, including multimeters, power supplies, and electronic loads. This laboratory exercise is part of a third semester undergraduate course in physical chemistry and can be completed in a single laboratory session. Student feedback shows that the experimental work, coupled with a written report, significantly broadens student understanding of the electrochemistry of batteries.

The 3D Zn(II) coordination polymer {[Zn3(L)(4,4′-bpy)]}n (GTU-3) was prepared with a novel hexapod-shaped molecular building block, hexakis(methyl-2-(4-phenoxyphenyl)acetatebenzene) cyclotriphosphazene (H6L1) by solvothermal reaction in dimethylformamide (DMF). Zn(II) coordination polymer was characterized by FTIR, thermal analysis, SEM-EDX, BET, powder X-ray diffraction analysis, and single crystal X-ray diffraction techniques. GTU-3 consists of six crystallographically independent Zn2+ ions, two fully deprotonated cyclophosphazene-based ligands, and two 4,4′-bipyridines (4,4′-bpy). In the complex, the flexible multisite cyclotriphosphazene bridging ligand (H6L) was completely deprotonated. GTU-3 exhibited relatively good catalytic activity toward Rhodamine B (RhB) removal in aqueous solution. A 0.4 g/L amount of GTU-3 could degrade the 10 mg/L solution of RhB up to 76.5% in the presence of peroxymonosulfate (PMS) oxidant in 1 h. The kinetic studies showed that the degradation process followed pseudo-first-order kinetic. By extending the degradation time to 5 h, the degradation efficiency reached 95.3%. Under the same conditions, Methylene Blue (MB) and Acid Red 17 (AR17) dyes were degraded by 86.2% and 52.8%, respectively.