Application of apophyllite and thomsonite natural zeolite as modified adsorbents for the removal of zinc from acid mine drainage.

Materials composed of natural zeolite have the potential to serve as highly effective adsorbents in the treatment of wastewater. The present study explores zeolite resin-based Apophyllite and Thomsonite as adsorbents for removing Zinc from acid mine drainage solution. The characteristics of the natural zeolites (Apophyllites and Thomsonite) are investigated using X-ray diffraction, Fourier-transform infrared spectroscopy and Field emission scanning electron microscopy analysis. The removal of Zinc from AMD is explored, and the influence of metal ion concentration, resin dose, and pH is investigated using a batch exchange resin-based experimental method. Maximum zinc removal occurs in the pH range of 2-6 with an initial zinc content of 50-250 mg/L and a resin dosage of 25-700 mg/L, indicating that the adsorption process is pH-dependent. Various isotherm models, including those proposed by Freundlich and Langmuir as well as Redlich-Peterson, Dubinin, and Temkin, are used to verify the results of the experimental research. All these isotherm models' constants are determined. Both resins showed different sorption efficiencies at different operating conditions. However, highest Zn removal efficiency of 86.2% was observed for the Thomsonite zeolite resin whereas Apophyllite zeolite resin showed maximum Zn uptake of 81.6%. Thus, Thomsonite was found to be an effective sorbent.

ZIF-8 decorated cellulose acetate mixed matrix membrane: An efficient approach for textile effluent treatment.

The textile industry is the second largest water-intensive industry and generates enormous wastewater. The dyes and heavy metals present in the textile effluent, even at their lower concentrations, can cause an adverse effect on the environment and human health. Recently, mixed matrix membranes have gained massive attention due to membrane property enhancement caused by incorporating nanofillers/additives in the polymer matrix. This current study examines the efficacy of ZIF-8/CA membrane on dye removal and treatment of real-time textile industry effluent. Initially, ZIF-8 nanoparticles were synthesized using a probe sonicator. The XRD, FT-IR, and SEM analysis confirmed the formation of crystalline and hexagonal facet ZIF-8 nanoparticles. The ZIF-8 nanoparticles were dispersed into a cellulose acetate matrix, and a membrane was prepared using the "phase inversion method." The membrane was characterized using FT-IR and SEM analysis, which endorse incorporating ZIF-8 into the polymer matrix. Later, the efficacy of the ZIF-8/CA membrane was verified by dye removal studies. The dye removal studies on crystal violet, acid red 13, and reactive black 5 reveal that the membrane is ∼85% efficient in dye removal, and the studies were further extended to real-time textile effluent treatment. The studies on textile effluent prevail that ZIF-8/CA membrane is also proficient in removing chemical oxygen demand (COD) ∼70%, total organic carbon (TOC) ∼80%, and heavy metals such as lead, chromium, and cadmium from textile wastewater and proved to be efficient in treating the textile effluent.

Recent progress in chromium removal from wastewater using covalent organic frameworks - A review.

Covalent organic frameworks (COFs) offer a pivotal solution to urgently address heavy metal removal from wastewater due to their exceptional attributes such as high adsorption capacity, tunable porosity, controllable energy band structures, superior photocatalytic performance, and high stability-reusability. Despite these advantages, COFs encounter certain challenges, including inefficient utilization of visible light, rapid recombination of photogenerated carriers, and limited access to active sites due to close stacking. To enhance the photocatalytic and adsorptive performance of COF-based catalysts, various modification strategies have been reported, with a particular focus on molecular design, structural regulation, and heterostructure engineering. This review comprehensively explores recent advancements in COF-based photocatalytic and adsorptive materials for chromium removal from wastewater, addressing kinetics, mechanisms, and key influencing factors. Additionally, it sheds light on the influence of chemical composition and functional groups of COFs on the efficiency of hexavalent chromium [Cr (VI)] removal.

Preparation of coated MgFe layered double hydroxide nanoparticles on cement kiln dust and intercalated with sodium dodecyl sulfate as an intermediate layer for the adsorption of estrogen from water.

Estrogenic hormones, found as micropollutants in water systems, give rise to grave concerns for human health and marine ecosystems, triggering a cascade of adverse effects. This research presents an innovative manufacturing approach using nanoscale layered double hydroxides of magnesium and iron, with sodium dodecyl sulfate surfactant, to create highly efficient sorbent cement kiln dust (CKD) based beads (CKD/MgFe-SDS-LDH-beads). These beads effectively remove estrone from water. Optimization of the preparation process considered factors like molar Mg/Fe ratio, CKD dosage, pH, and SDS dosage using Response Surface Methodology (RSM). The adsorption process was well-characterized by Langmuir isotherm and pseudo-second-order kinetic models, demonstrating a remarkable 6.491 mg/g sorption capacity. Results proved that the calcite was the main component of the CKD with miners of dolomite, and quartz. Adsorption capacity, surface charges, and the availability of vacant sites may be the main mechanisms responsible of removal process. Experimental tests confirmed the beads' potential for estrone removal, aligning with the Bohart-Adams and Thomas-BDST models. This study introduces a promising, eco-friendly solution for addressing water contamination challenges.

Subsurface flow constructed wetlands for treating of simulated cadmium ions-wastewater with presence of Canna indica and Typha domingensis.

The presence of toxic cadmium ions in the wastewater resulted from industrial sector forms the critical issue for public health and ecosystem. This study determines the ability of four vertical subsurface flow constructed wetlands units in the treatment of simulated wastewater laden with cadmium ions. This was achieved through using sewage sludge byproduct as alternative for the traditional sand to be substrate for aforementioned units in order to satisfy the sustainable concepts; however, Canna indica and Typha domingensis can apply to enhance the cadmium removal. The performance of constructed wetlands has been evaluated through monitoring of the pH, dissolved oxygen (DO), temperature, and concentrations of cadmium (Cd) in the effluents for retention time (0.5-120 h) and metal concentration (5-40 mg/L). The results demonstrated that the Cd removal percentage was exceeded 82% beyond 5 days and for concentration of 5 mg/L; however, this percentage was decreased with smaller retention time and higher metal concentration. The Grau second-order kinetic model accurately simulated the measurements of effluent Cd concentrations as a function of retention times. The FT-IR analysis indicated the existence of certain functional groups capable of enhancing the Cd removal. The treated wastewater's pH, DO, temperature, total dissolved solids (TDS), and electrical conductivity (EC) all meet the requirements for irrigation water.

Complete arsenite removal from groundwater by UV activated potassium persulfate and iron oxide impregnated granular activated carbon.

Removal of toxic arsenite [As(III)] from the contaminated surface and groundwater is essential for human health. However, direct arsenite removal is difficult compared to arsenate [As(V)]. Therefore, the peroxidation of arsenite to arsenate is vital for its effective removal from water. Herein, we investigated the removal efficiency of arsenic from groundwater by oxidizing it with UV activated potassium persulfate (KPS) and subsequently adsorbing it on iron oxide impregnated granular activated carbon (FeO/GAC). A batch experiment was carried out to determine the adsorption kinetics and thermodynamics. Further, the effects of the adsorbent mass (FeO/GAC), C/Fe molar ratio, pH, arsenic concentration, competing anions, and humic acid in arsenic adsorption was studied. The characterization of FeO/GAC adsorbent was investigated by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Brunauer-Emmett-Teller (BET), and zeta potential measurements. Using the UV activated KPS and FeO/GAC, a ∼100% removal amount was achieved for 10 ppm of the arsenic solution in 1 h. Also, the effect of pH showed the highest removal efficiency in the pH range of 6.0-7.0 and it decreased dramatically at higher and lower pH values. The groundwater collected from Cheongyang in South Korea was spiked with 10 ppm of the arsenic (III) and more than 82% removal of arsenic was achieved in 90 min even in the presence of natural contaminants. Therefore, the results suggest that the UV activated KPS with FeO/GAC provides an effective method for treating highly-arsenic-contaminated water sources and this may be a viable alternative method over the existing methods.

Influence of Ag nanoparticles anchored on protonated g-C3N4-Bi2MoO6 nanocomposites for effective antibiotic and organic pollutant degradation.

The development of noble metal-anchored semiconductors for photocatalytic processes is now garnering interest for potential application to toxic pollutants as well as antibiotic degradation. Herein, we report novel Ag@p-g-C3N4-Bi2MoO6 nanocomposites synthesized by facile hydrothermal and calcination methods with a size of about 50 nm, exhibiting superior photocatalytic activity for charge separation. The resulting nanocomposites were evaluated by various physiochemical techniques such as X-ray diffraction, X-ray photoelectron spectroscopy, Fourier-transform infrared spectroscopy, scanning electron microscopy, and high-resolution transmission electron microscopy. The charge transfer photogenerated carriers were confirmed by photoluminescence spectra and electrochemical impedance spectroscopy. The anchoring of Ag nanoparticles over p-g-C3N4/Bi2MoO6 decreased the band gap energy from 2.67 to 2.48 eV, to exhibit an abnormal increase in absorption of light towards the visible light region. The degradation performance of the nanocomposites in terms of antibiotic ciprofloxacin and rhodamine B degradation efficiency was measured 85 and 99.7% respectively. The superoxide radical anion ˙O2 - played a significant role throughout the entire degradation process. Focusing on the probable mechanism based on the desirable results, the present work follows the heterostructure mechanism. Moreover, this work features the feasible applications of Ag@p-g-C3N4-Bi2MoO6 as a modified photocatalyst in the treatment of both domestic and industrial waste water.

Correction to "Environmentally Sustainable Synthesis of CoFe2O4-TiO2/rGO Ternary Photocatalyst: A Highly Efficient and Stable Photocatalyst for High Production of Hydrogen (Solar Fuel)".

[This corrects the article DOI: 10.1021/acsomega.8b03221.].

Environmentally Sustainable Synthesis of a CoFe2O4-TiO2/rGO Ternary Photocatalyst: A Highly Efficient and Stable Photocatalyst for High Production of Hydrogen (Solar Fuel).

Herein, a magnetically separable reduced graphene oxide (rGO)-supported CoFe2O4-TiO2 photocatalyst was developed by a simple ultrasound-assisted wet impregnation method for efficient photocatalytic H2 production. Integration of CoFe2O4 with TiO2 induced the formation of Ti3+ sites that remarkably reduced the optical band gap of TiO2 to 2.80 eV from 3.20 eV. Moreover, the addition of rGO improved the charge carrier separation by forming Ti-C bonds. Importantly, the CoFe2O4-TiO2/rGO photocatalyst demonstrated significantly enhanced photocatalytic H2 production compared to that from its individual counterparts such as TiO2 and CoFe2O4-TiO2, respectably. A maximum H2 production rate of 76 559 µmol g-1 h-1 was achieved with a 20 wt % CoFe2O4- and 1 wt % rGO-loaded TiO2 photocatalyst, which was approximately 14-fold enhancement when compared with the bare TiO2. An apparent quantum yield of 12.97% at 400 nm was observed for the CoFe2O4-TiO2/rGO photocatalyst under optimized reaction conditions. This remarkable enhancement can be attributed to synergistically improved charge carrier separation through Ti3+ sites and rGO support, viz., Ti-C bonds. The recyclability of the photocatalyst was ascertained over four consecutive cycles, indicating the stability of the photocatalyst. In addition, it is worth mentioning that the photocatalyst could be easily separated after the reaction using a simple magnet. Thus, we believe that this study may open a new way to prepare low-cost, noble-metal-free magnetic materials with TiO2 for sustainable photocatalytic H2 production.

Oxygen-Functionalized and Ni+x (x=2,†3)-Coordinated Graphitic Carbon Nitride Nanosheets with Long-Life Deep-Trap States and their Direct Solar-Light-Driven Hydrogen Evolution Activity.

Graphitic carbon nitride, a 2 D layered photocatalyst coupled with transition metal oxides often shows promising photocatalytic hydrogen evolution activity. However, low surface area and poor charge separation greatly hinder its photocatalytic efficiency. A Ni+x (x=2, 3)/O-g-C3 N4 photocatalyst with a very high specific surface area (199 m2 g-1 ) has been prepared by thermal condensation and wet-impregnation methods. The oxygen-functionalized and Ni+x (x=2, 3)-coordinated g-C3 N4 produced 1664 µmol g-1 of hydrogen evolution from water under direct solar light irradiation in 4 h, which is 23 times higher than that over O-g-C3 N4 . This significant enhancement results from the combined effects of large surface area, the formation of long-life deep-trap states, effective charge carrier separation, and extended visible light absorption. The separation and transport behavior of the charge carriers are investigated by photoluminescence, time-resolved photoluminescence, photocurrent and Mott-Schottky measurements. Additionally, the interaction between Ni+x (x=2, 3) and O-g-C3 N4 is studied by X-ray photoelectron spectroscopy, X-ray diffraction, and FTIR spectroscopy. The Ni+x (x=2, 3)/O-g-C3 N4 photocatalyst shows remarkable reusability over a period of two months (six cycles). This study may provide a pathway to simultaneously overcome the challenges of low surface area and poor charge separation in g-C3 N4 -based photocatalysts.

Ultrasound assisted synthesis of reduced graphene oxide (rGO) supported InVO4-TiO2 nanocomposite for efficient hydrogen production.

Herein, a ternary nanocomposite, comprising metal oxide (InVO4 and TiO2) photocatalysts supported on rGO sheets was prepared via the hydrothermal method in the presence and absence of ultrasound irradiation. The photocatalytic performance of the prepared rGO/InVO4-TiO2 nanocomposites was evaluated for H2 evolution activity from water splitting with glycerol as a sacrificial agent. Interestingly, a synergistic effect (6-fold) was observed with rGO/InVO4-TiO2 nanocomposite prepared with the help of ultrasound compared to the samples prepared without ultrasound. The optimized nanocomposite (rGO/InVO4-TiO2) exhibited a maximum H2 evolution of 1669 µmol h-1, a ∼13-fold enhancement compared to the bare TiO2. This remarkable enhancement is mainly due to the synergistic effect induced by ultrasonic irradiation along with the shifting of the optical band gap of TiO2 from 3.20 eV to 2.80 eV by loading of InVO4 and rGO and also strong chemical bonding between metal (Ti) and C through Ti-C bond formation, as identified by UV-vis DRS spectra and XPS spectra, respectively. Moreover, a significant quenching of PL emission intensity and smaller radius arc of the Nyquist plot in the EIS were observed when the rGO and InVO4 were loaded in TiO2, indicating the efficient charge carriers separation and transfer in the presence of rGO sheet, resulting in enhanced photocatalytic activity. Thus, application of ultrasound has played significant and important roles in substantially enhancing hydrogen evolution along with rGO and InVO4 acting as support and co-catalyst, respectively.

Synergistic effect of sono-photocatalytic process for the degradation of organic pollutants using CuO-TiO2/rGO.

Combinations of different Advanced Oxidation Processes (AOPs) are being exploited for waste water treatment. The usage of ultrasound in photocatalysis finds much attention as the combined process offers some advantages over individual processes. Herein, we report the ultrasound assisted photocatalytic degradation of an organic pollutant (methyl orange as a model dye) in the presence of CuO-TiO2/rGO photocatalyst which was prepared by a simple wet impregnation method. A synergistic effect (3.7-fold) was observed by combining the sonolysis and photocatalysis processes. Influence of Cu loading and graphene oxide (GO) dosage over the photocatalytic performance of TiO2 was examined in detail. The catalyst dosage and initial concentration of MO were optimized based on a series of experimental studies. Besides, neutral pH was found to show an optimum efficiency for this sono-photocatalytic process.