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In this paper, undoped and copper-doped ZnO nanoparticles (NPs) were successfully synthesized using a gliding arc discharge (GAD) plasma technique, which is a sustainable, cost-effective, and scalable method. This method offers several advantages over traditional synthesis methods. The synthesized NPs were characterized by various techniques to understand their physicochemical properties. XRD analysis confirmed the presence of characteristic peaks of pure ZnO, while doped samples exhibited additional peaks corresponding to CuO crystal planes, indicating the successful incorporation of Cu into the lattice. As obvious, bare ZnO showed absorption peak at 378 nm corresponding to the band gap of 3.21 eV. The band gap of Cu-doped samples increased systematically, i.e., 3.35 eV for 2% Cu, 3.47 eV for 4% Cu, and 3.66 eV for 6% Cu. SEM images revealed aggregation and increase in particle size with the increasing in Cu concentration. EDAX analysis revealed a decrease in the weight percentage of oxygen and zinc with the increase in Cu concentration, suggesting structural changes within the lattice. Furthermore, the antibacterial activity against Gram-positive and Gram-negative bacteria, antioxidant activity, and photocatalytic activity against three different organic dyes such as Brilliant Cresyl Blue (BCB), Methylene Blue (MB), and Congo Red (CR) was studied. It is found that the photocatalytic activity of ZnO NPs varies with Cu concentration, leading to a decrease in its performance. The antibacterial activity of the NPs was also assessed, with undoped ZnO NPs showing dose-dependent effects against bacteria, while the Cu-doped ZnO NPs exhibited decreased efficacy. Interestingly, Cu doping significantly enhanced the antioxidant activity of the NPs compared to the undoped ZnO. [ABSTRACT FROM AUTHOR]

Herein, a Bi2S3/Cu2S was successfully synthesized via a simple one-step wet impregnation process. The compositional behavior and electrical and optical properties of photocatalysts were investigated in detail. Photocatalytic technology has shown great promise in wastewater treatment, splitting water to hydrogen, and converting CO2 to fuel. Researchers or scientist are attempting to design sulfate-based heterojunction photocatalytic systems in order to develop novel photocatalysts with excellent performance. Photodegradation of methylene blue (MB) dye and tetracycline (TC) drug under visible light irradiation was used to assess the photocatalytic activity of as-prepared samples. As a result, 2:1% wt of Bi2S3/Cu2S heterostructure composite revealed superior visible light degradation performing of MB dye, and TC drug efficiency as 90.2% and 87.5%, respectively. The prepared hybrid photocatalyst has demonstated a potential for use in the photocatalytic degradation of antibiotic durgs and dyes, indicating a promissing future for its application. [ABSTRACT FROM AUTHOR]

Together with the rapid growth of technology, the discharge of wastewater from industry into environment had become a hot topic among society nowadays. More attention had been given to the development of water treatment techniques. In this study, sonocatalysis was proposed to degrade the organic pollutants using silver-doped zinc oxide (Ag-ZnO) nanoparticles which were synthesized via green synthesis process using Clitoria ternatea Linn (Asian Pigeonwings flower). The characterization results revealed that the incorporation of Ag into the ZnO lattice decreased the crystallite size and increased the specific surface area of ZnO nanoparticles. It is noteworthy that about 98% of sonocatalytic degradation efficiency of malachite green (MG) was successfully achieved within 30 min in the presence of 5 wt.% Ag-ZnO with 1.0 g/L of catalyst loading under 500 mg/L of initial dye concentration, 80 W of ultrasonic power, 45 kHz of ultrasound frequency, and 2.0 mM of oxidant concentration. The kinetic study showed that the sonocatalytic degradation of organic dye was fitted well into second-order kinetic model with high R2 value (0.9531). In the thermodynamic study, negative value of standard Gibbs free energy and low value of activation energy (+ 24.43 kJ/mol) were obtained in the sonocatalytic degradation of MG using the green-synthesized Ag-ZnO sample. Highlights: • Facile synthesis of silver-doped zinc oxide nanoparticles using plant extract which act as reducing and stabilizing agents • Optical, physical, and chemical characterization of green-synthesized nanomaterials were performed • Evaluation of sonocatalytic degradation of organic dye using green-synthesized nanomaterials • Sonocatalytic behavior, kinetic and thermodynamic studies of sonocatalytic reaction [ABSTRACT FROM AUTHOR]

Water pollutants of non-biodegradable toxic aromatic dye including Methylene blue (MB) and Rhodamine (RhB) are extremely carcinogenic thiazines used in various industries such as leather industry, paper industry, and the dyeing industry. The presence of dyes in wastewater causes severe threats to human health that are responsible for various harmful chronic or acute diseases and also shows an adverse impact on the environment as it reduces transparency and is harmful to water microorganisms. To overcome severe issues, many traditional techniques have been used to remove toxic pollutants, but these methods are insufficient to remove chemically stable dyes that remain in the treated wastewater. However, the photocatalytic degradation process is an efficient approach to degrade the dye up to the maximum extent with improved efficiency. Therefore, in this work, a new class of two-dimensional (2D) transition metal carbide of Titanium Carbide (Ti3C2Tx) MXene material was used for the organic dyes degradation such as MB and RhB using a photocatalytic process. A layered structure of hexagonal lattice symmetry of Ti3C2Tx MXene was successfully synthesized from the Titanium Aluminum Carbide of Ti3AlC2 bulk phase using an exfoliation process. Further, the XRD spectrum confirms the transformation of bulk MAX phase having (002) plane at 9.2° to Ti3C2Tx MXene of (002) plane at 8.88° confirms the successful removal of Al layer from MAX phase. A smooth, transparent, thin sheet-like morphology of Ti3C2Tx nanosheet size were found to be in the range of 70 to 150 nm evaluated from TEM images. Also, no holes or damages in the thin sheets were found after the treatment with strong hydrofluoric acid confirms the formation Ti3C2Tx layered sheets. The synthesized Ti3C2Tx MXene possesses excellent photocatalytic activity for the degradation of dyes MB, RhB, and mixtures of MB and RhB dyes. MB dye degraded with a degradation percentage efficiency of 99.32% in 30 min, while RhB dye was degraded upto 98.9% in 30 min. Also, experiments were conducted for degradation of mixture of MB and RhB dyes by UV light, and the degradation percentage efficiency were found to be 98.9% and 99.75% for mixture of MB and RhB dye in 45 min, respectively. Moreover, reaction rate constant (k) was determined for each dye of MB, RhB, and mixtures of MB and RhB and was found to be 0.0215 min−1 and 0.0058 min−1, and for mixtures, it was 0.0020 min−1 and 0.009 min−1, respectively. [ABSTRACT FROM AUTHOR]

Toxic organic dyes (colorants) are one of the main causes of water pollution that releases destructive effluents in the environment. To overcome this issue, a fundamental need to produce a novel, efficient catalyst for the degradation and mineralization of dye mixtures has arisen. The objective of this research is to develop an eminent Ni-doped magnetic carbon aerogel (Ni-MCA) catalyst using graft co-polymerization method having xanthan gum as backbone doped with Ni-magnetic nanoparticles (Ni-MNPs), that do not show agglomeration and easy to separate. The examination revealed that Ni-MCA provided exceptional magnetic characteristics (Ms = 52.75 emu/g) and potent catalytic activity for the degradation of mono- as well as binary-dye solutions of Congo red (CR) and methyl green (MG) dyes. The formation was verified by various characterization techniques such as FTIR, VSM, XRD, XPS, SEM, TEM, and EDX mapping. Interestingly, Ni-MCA shows faster result on anionic dye CR up to 97% with degradation rate of 5.647 × 10−1 min−1, and MG dye shows degradation of 95.7% with the degradation rate of 2.169 × 10−1 min−1, while dye mixture is showing 90% degradation with rate of 2.159 × 10−1 min−1. [ABSTRACT FROM AUTHOR]

The need to effectively remove toxic organic dyes from aquatic systems has become an increasingly critical issue in the recent years. In pursuit of this objective, polydopamine (PDA)-binary ZIF-8/UiO-66 (MOFs) was synthesized and incorporated into cellulose acetate (CA), producing ZIF-8/UiO-66/PDA@CA composite nanofibers under meticulously optimized conditions. The potential of fabricated nanofibers to remove cationic methylene blue (MB) dye was investigated. Various analysis tools including FTIR, XRD, SEM, zeta potential, BET, tensile strength testing, and XPS were employed. Results revealed a substantial leap in tensile strength, with ZIF-8/UiO-66/PDA@CA registering an impressive 2.8 MPa, as a marked improvement over the neat CA nanofibers (1.1 MPa). ZIF-8/UiO-66/PDA@CA nanofibers exhibit an outstanding adsorption capacity of 82 mg/g, notably outperforming the 22.4 mg/g capacity of neat CA nanofibers. In binary dye systems, these nanofibers exhibit a striking maximum adsorption capacity of 108 mg/g, establishing their eminence in addressing the complexities of wastewater treatment. Furthermore, the adsorption data fitted to the Langmuir isotherm, and the pseudo-second-order kinetic model. The fabricated nanofiber demonstrates good reproducibility and durability, consistently upholding its performance over five cycles. This suite of remarkable attributes collectively underscores its potential as a robust, durable, and highly promising solution for the effective and efficient removal of pernicious MB dye, in the context of both water quality improvement and environmental preservation. [ABSTRACT FROM AUTHOR]

Recently, visible-light-driven photocatalysis attracts much concerns in the remediation of environmental organic pollutants. In this study, the cerium doped biochar was fabricated through the hydrothermal method, and served as an efficient photocatalyst towards rhodamine B degradation under visible light irradiation. Almost 100% of rhodamine B was removed by 2.0 g·L−1 cerium doped biochar after 60 min of visible light irradiation at pH 3, but only about 25.50% and 29.60% of rhodamine B was removed by cerium dioxide and biochar under identical conditions. The degradation process coincided well with the pseudo-first-order kinetic model, and the photodegradation rate constant of cerium doped biochar was 0.0485·min−1, which was respectively 97 and 44 times that of biochar (0.0005·min−1) and cerium dioxide (0.0011·min−1). According to the trapping experiments and electron spin resonance spectroscopy analysis, h+, O2−∙ and ∙OH all participated in the degradation of rhodamine B in the cerium doped biochar photocatalytic systems, and the function of h+ and ∙OH was dominated. Consequently, the biochar could not only be an excellent carrier for supporting cerium dioxide, but also greatly improved its photocatalytic activity. The band gap of cerium doped biochar was narrower than cerium dioxide, which could improve the separation and migration of photogenerated electron–hole pairs under visible-light excitation, thus ultimately enhanced the degradation of rhodamine B. This work provided a deeper understanding of the preparation of biochar-based photocatalyst and its application in the remediation of environmental organic pollution. [ABSTRACT FROM AUTHOR]

Toxic organic dyes-containing wastewater treatment by adsorption and photocatalytic techniques is widely applied, but adsorbents and photocatalysts are often synthesized through chemical methods, leading to secondary pollution by released chemicals. Here, we report a benign method using Tecoma stans floral extract to produce MgFe2O4/ZnO (MGFOZ) nanoparticles for adsorption and photocatalytic degradation of coomassie brilliant blue (CBB) dye. Green MGFOZ owned a surface area of 9.65 m2/g and an average grain size of 54 nm. This bio-based nanomaterial showed higher removal percentage and better recyclability (up to five cycles) than green MgFe2O4 and ZnO nanoparticles. CBB adsorption by MGFOZ was examined by kinetic and isotherm models with better fittings of Bangham and Langmuir or Temkin. RSM-based optimization was conducted to reach an actual adsorption capacity of 147.68 mg/g. Moreover, MGFOZ/visible light system showed a degradation efficiency of 89% CBB dye after 120 min. CBB adsorption can be controlled by both physisorption and chemisorption while •O2- and •OH radicals are responsible for photo-degradation of CBB dye. This study suggested that MGFOZ can be a promising adsorbent and catalyst for removal of organic dyes in water. [ABSTRACT FROM AUTHOR]

Development of nanocomposites as efficient photocatalysts for the removal of hazardous organic pollutants is always in dire demand due to increase in water pollution. In this article, a facile sol-gel method has been used to synthesize cerium oxide (CeO2) nanoparticles followed by their decoration over multi-walled carbon nanotubes (CNTs) and graphene oxide (GO) to construct binary as well ternary hybrid nanocomposites using ultrasonic treatment. The oxygen vacancy defects have been depicted using X-ray photoelectron spectroscopy (XPS) that may result into improved photocatalytic efficiency. The ternary hybrid nanocomposites (CeO2/CNT/GO) showed excellent photocatalytic efficiency towards degradation of rose bengal (RB) dye up to 96.9% in 50 min. CNTs and GO provide the interfacial charge transfer which inhibits the electron-hole pair recombination. The results obtained here indicate that these composites can be effectively utilized as promising materials for the degradation of harmful organic pollutants for wastewater treatment. [ABSTRACT FROM AUTHOR]

Natural dyes have been widely employed in the fabrication of dye-sensitized solar cells (DSSCs). DSSCs are favored for their cost-effective, and simple fabrication process relies on metal-based and organic dyes. The choice of dyes greatly affects the performance of DSSCs. DSSCs have found a lot of applications in indoor, solar power gadgets with reasonable efficiency up to 13%. Nonetheless, despite advances in DSSC technology, the complex photophysics and excited state dynamics associated with natural dyes employed in DSSCs remain elusive and have not been adequately investigated. This information gap emphasizes the need for more study and analysis into the behavior of these dyes, since understanding their underlying principles might lead to major improvements in DSSC performance and efficiency. In this work, we have investigated the fundamental characteristics and excited-state carrier dynamics of natural dye curcumin using ultrafast transient absorption (TA) spectroscopy technique. The curcumin dye shows delay time-dependent positive and negative signals in the TA spectra, which are related to excited state absorption and stimulated emission. We also found that hydrogen bonding and polarity effect of solvent significantly influence the carrier dynamics of curcumin. Ultrafast lifetime component indicates that hydrogen-bond rearrangements are involved in the kinetics of the relaxation process of the S1 state of curcumin photo-sensitizer. [ABSTRACT FROM AUTHOR]

A functionalized gum acacia–activated carbon-CaO/NiO nanocomposite was synthesized using an eco-friendly sol–gel method. The formed nanocomposite was designed to apply various light sources to enhance the improved removal of organic dyes such as methylene blue, methyl orange, methyl red, and rhodamine B from aqueous media. The band gap energies of CaO, NiO nanoparticles and gum acacia–activated carbon were 3.54, 4.28, and 5.34 eV, respectively, corresponding to a reflection edge of 350, 290, and 232 nm, respectively. The surface area of the synthesized nanocomposite was measured to be 17.892 m2 g−1. Sunlight and 20 mg L−1 of the nanocomposite quenched the dyes (methylene blue, 99.7%; methyl orange, 98.3%; methyl red, 96.7%; and rhodamine B, 93.5%) after 120, 100, 100, and 75 min of irradiation, respectively. However, after 80, 100, 100, and 75 min, the percentage of dyes under UV light irradiation was 98.6%, 95.8%, 98.4%, and 94.2% for methylene blue, methyl orange, methyl red, and rhodamine B, respectively. The nanocomposite showed excellent stability after five cycles of dye reduction. [ABSTRACT FROM AUTHOR]

In this work, we have fabricated a novel Fenton-like ferrihydrite/MoS2 (Fh/MoS2) composite and verified that the introduction of a small amount of iron on the surface of MoS2 can directly promote the exposure of Mo4+, finally enhancing the catalytic activity of the catalyst. Even though the content of iron element is only 1.19% in the composite, the reaction rate constant of Fh/MoS2 system for the degradation of environmental pollutants, such as organic dyes, antibiotic, and ionic liquid, is all much better than that of pure MoS2 system, which is attributed to much more generation of reactive oxygen species derived from synergistic effect of Fe3+/Fe2+ and Mo4+/Mo6+ redox cycles. The results of XPS and low-temperature EPR confirm that the exposure amount of Mo4+ active sites of 10% Fh/MoS2 is greatly increased, which is conducive to the conversion of Fe3+ to Fe2+ in the reaction process, thus effectively promoting the activation of H2O2. [ABSTRACT FROM AUTHOR]

The importance of water for all living organisms is unquestionable and protecting its sources is crucial. In order to reduce water contaminants, like toxic metals and organic dyes, researchers are exploring different techniques, such as adsorption, photocatalytic degradation, and electrolysis. Novel materials are also being sought. In particular, biopolymers like guar gum and xanthan gum, that are eco-friendly, non-toxic, reusable, abundant and cost-effective, have enormous potential. Gum-based nanocomposites can be prepared and used for removing heavy metals and colored dyes by adsorption and degradation, respectively. This review explains the significance of gum-based nanomaterials in waste water treatment, including preparative steps, characterization techniques, kinetics models, and the degradation and adsorption mechanisms involved. [ABSTRACT FROM AUTHOR]

We synthesized a γ-irradiated chitosan-ZnO-AgNPs (ICZA) composite by using a simple hydrogels method. We evaluated its adsorption/photocatalytic degradation abilities for the removal of an organic dye and its antibacterial activity. The XRD, SEM, TEM, EDS, and FTIR techniques were used to characterize the obtained samples. Based on the adsorption and degradation of methylene blue (MB) in the dark and under UV light irradiation, the adsorption and the photocatalytic activity of the as-obtained samples were evaluated. The optimum conditions for synthesizing the composite were as follows: contact time of 210 min, a dosage of 2 g/L, MB concentration of 40 mg/L, and a solution pH of 8.0. The ICZA had a high adsorption capacity, which was suitable for removing MB from the aqueous solutions; it showed a maximum adsorption capacity (qm) of 92.59 mg/g. The fit of the adsorption isotherms with the Langmuir model was satisfactory. The photocatalytic degradation ability of the composite was also better than that of other catalysts in the presence of UV light, with an apparent rate constant (kapp) of 3.08 × 10−2. The synthesized ICZA also showed good antibacterial activity against Staphylococcus aureus, with a minimum inhibitory concentration (MIC) and a minimum bactericidal concentration (MBC) of 12.5 g/mL and 50 g/mL under light-incubation and dark-incubation conditions. Finally, we discussed the hypothesized mechanism of the adsorption/photocatalytic activity and antibacterial activity of the ICZA composite in this study. [ABSTRACT FROM AUTHOR]

Water pollution caused by organic dyes is one of the greatest threats to the ecosystem. The removal of dyes from water has remained a challenge for scientists. Recently, metal sulphides have emerged as a potential candidate for water remediation applications. The efficient charge transportation, greater surface-active sites, and low bandgap of metal sulphides make them an excellent choice of semiconductor photocatalysts for degradation of dyes. This review summarises the potential application of metal sulphides and their heterojunctions for the photocatalytic degradation of organic dyes from wastewater. A detailed study has been presented on the synthesis, basics of photodegradation and heterojunctions and photocatalytic activity. The effect of the use of templates, doping agents, synthesis route, and various other factors affecting the photocatalytic activity of metal sulphides have been summarised in this review. The synthesis techniques, characterisation techniques, mechanism of degradation of organic dyes by Z-scheme heterojunction photocatalyst, reusability and stability of metal sulphides, and the scope of future research are also discussed. This study indicates that Scopus-based core gathered data could be used to give an objective overview of the global dye degradation research from 2008 to 2023 (15 years). All data (articles, authors, keywords, and publications) is compiled in the Scopus database. For the bibliometric study, 1962 papers relevant to dye photodegradation by sulfide-based photocatalysts were found, and this number rises yearly. A bibliometric analysis provides a 15-year evaluation of the state-of-the-art research on the impact of metal sulfide-based photocatalysts on the photodegradation of dyes. [ABSTRACT FROM AUTHOR]

The intent of this research work is to implement a biogenic, affordable, and highly effective Ce-Ni@biochar catalyst in order to study its photoactivity in the removal of crystal violet and malachite green oxalate. The catalyst was synthesized using liquid phase reduction method where cerium and nickel nanoparticles are embedded on the rice husk biochar for photocatalytic degradation of organic dyes in the presence of sunshine. Various characterization techniques were conducted on fabricated catalyst for adequate evaluation of the chemical composition as well as morphological and topographical properties of the formed compound. The nanoparticles embedded on biochar persuade increased charge separation that resulted in a substantial decrease in electron-hole recombination rate. The synergistic actions of the catalyst resulted in a high level of photocatalytic activity. The fabricated nanocatalyst showed excellent photoactivity that caused 96 and 99% degradation of crystal violet and malachite green oxalate, a growing industrial pollutant, within 35 and 25 min, respectively. A persuasive mechanism and kinetics are well presented. A series of investigations were done on other factors, such as contact duration, catalyst dosage, starting concentration, interfering ions, and pH, to know its degradation pursuance. The impacts of different water matrices were also investigated. The removal effectiveness of the synthesized catalyst persisted after five consecutive cycles. Marking the burgeoning industrial effluents as a result of rapid industrialization and also focusing on easy availability and low-cost source as well as high efficiency, reusability of the catalyst imparts its novelty and need of this research work. [ABSTRACT FROM AUTHOR]

The present study proposed the synthesis of low-toxicity and eco-friendly spherically shaped manganese oxides (α-MnO2, Mn2O3, and Mn3O4) by using the chemical precipitation method. The unique variable oxidation states and different structural diversity of manganese-based materials have a strong effect on fast electron transfer reactions. XRD, SEM, and BET analyses were used to confirm the structure morphology, higher surface area, and excellent porosity. The catalytic activity of as-prepared manganese oxides (MnOx) was investigated for the rhodamine B (RhB) organic pollutant with peroxymonosulfate (PMS) activation under the condition of control pH. In acidic conditions (pH = 3), complete RhB degradation and 90% total organic carbon (TOC) reduction were attained in 60 min. The effects of operating parameters such as solution pH, PMS loading, catalyst dosage, and dye concentration on RhB removal reduction were also tested. The different oxidation states of MnOx promote the oxidative–reductive reaction under acidic conditions and enhance the SO4•−/•OH radical formation during the treatment, whereas the higher surface area offers sufficient absorption sites for interaction of the catalyst with pollutants. A scavenger experiment was used to investigate the generation of more reactive species that participate in dye degradation. The effect of inorganic anions on divalent metal ions that genuinely occur in water bodies was also studied. Additionally, separation and mass analysis were used to investigate the RhB dye degradation mechanism at optimum conditions based on the intermediate's identification. Repeatability tests confirmed that MnOx showed superb catalytic performance on its removal trend. [ABSTRACT FROM AUTHOR]

Globally, treating and disposing of industrial pollutants is a techno-economic challenge. Industries' large production of harmful heavy metal ions (HMIs) and dyes and inappropriate disposal worsen water contamination. Much attention is required on the development of efficient and cost-effective technologies and approaches for removing toxic HMIs and dyes from wastewater as they pose a severe threat to public health and aquatic ecosystems. Due to the proven superiority of adsorption over other alternative methods, various nanosorbents have been developed for the efficient removal of HMIs and dyes from wastewater and aqueous solutions. Being a good adsorbent, conducting polymer-based magnetic nanocomposites (CP-MNCPs) has drawn more attention for HMIs and dye removal. Conductive polymers' pH-responsiveness makes CP-MNCP ideal for wastewater treatment. The composite material absorbed dyes and/or HMIs from contaminated water could be removed by changing the pH. Here, we review the production strategies and applications of CP-MNCPs for HMIs and dye removal. The review also sheds light on the adsorption mechanism, adsorption efficiency, kinetic and adsorption models, and regeneration capacity of the various CP-MNCPs. To date, various modifications to conducting polymers (CPs) have been explored to improve the adsorption properties. It is evident from the literature survey that the combination of SiO2, graphene oxide (GO), and multi-walled carbon nanotubes (MWCNTs) with CPs-MNCPs enhances the adsorption capacity of nanocomposites to a large extent, so future research should lean toward the development of cost-effective hybrid CPs-nanocomposites. [ABSTRACT FROM AUTHOR]

In this paper, nanocomposite NiO/Cr2O3 has been synthesized by a simple chemical reduction method to study its photocatalytic activity under sunlight irradiation. Various advanced analytical techniques including powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive spectroscopy (EDS), elemental mapping, Fourier transform infrared spectroscopy (FTIR), and UV-visible spectroscopy have been utilized to characterize the synthesized NiO/Cr2O3 nanocomposite. SEM images show the sheet-shaped morphology of NiO/Cr2O3 nanocomposite. These sheets have a rough surface with nano to micro size cracks. These cracks play important role in the enhancement of photocatalytic activity by increasing surface active sites for the adsorption of dye molecules on the surface of the photocatalyst. The organic dyes crystal violet (CV) and methylene blue (MB) have been chosen to study the photocatalytic behavior of NiO/Cr2O3 nanocomposite under sunlight irradiation. The photocatalytic efficiency of NiO/Cr2O3 nanocomposite has been obtained 88.47% and 93.63% against crystal violet and methylene blue respectively. The results of the photocatalytic kinetics exhibit that degradation rate constant value for crystal violet dye is higher as compared to methylene blue dye. Obtained kinetic results indicate that synthesized nanocomposite acts as an efficient photocatalyst for the degradation of both crystal violet dye and methylene blue dye. NiO/Cr2O3 nanocomposite also exhibited reusability and stability for photocatalytic degradation of both organic dyes. Photoelectrochemical measurements as photocurrent, electrochemical impedance spectroscopy (EIS), and Mott-Schottky plot were also performed for synthesized NiO/Cr2O3 nanocomposite. Consequently, this synthesized NiO/Cr2O3 nanocomposite can be utilized for environmental remediation of harmful dyes. [ABSTRACT FROM AUTHOR]

Fabrication of heterojunction semiconductors for the photodegradation of toxic organic dyes under sunlight exposure has earned significant recognition from researchers nowadays. On that account, we have synthesized and explored a comparative photodegradation study of ZnO/CuO nanocomposite with ZnO and CuO nanoparticles. ZnO and CuO nanoparticles have been synthesized by biosynthesis methods using Ficus benghalensis leaf extract. As-synthesized ZnO and CuO nanoparticles have been further utilized for the synthesis of ZnO/CuO nanocomposite by the mortar pestle crushing/milling method. Both biosynthesis methods and mortar pestle crushing/milling methods are simple, low-cost, and environmentally friendly. Structural, optical, and morphological analysis of all the synthesized nanomaterials have been done by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer–Emmett–Teller (BET), field emission scanning electron microscopy (FESEM), energy-dispersive spectroscopy (EDS), fourier transform infrared spectroscopy (FTIR), and UV–visible spectroscopy. PXRD data reveal that synthesized ZnO nanoparticles are in the hexagonal wurtzite phase, CuO nanoparticles in the monoclinic phase, and ZnO/CuO nanocomposite in the hexagonal wurtzite as well as in monoclinic phase. FE-SEM and TEM images of ZnO/CuO nanocomposite reveal the nanorod-shaped morphology along with micro-sized and nano-sized flakes. The BET analysis shows the surface areas 18.128 m2/g for ZnO nanoparticles, 16.653 m2/g for CuO nanoparticles, and 19.580 m2/g for ZnO/CuO nanocomposite, respectively. The energy band gap values of ZnO/CuO nanocomposite are obtained 3.13 eV for ZnO and 2.76 eV for CuO, respectively. The photocatalytic behaviors of all the synthesized nanomaterials are examined against aqueous dye solutions of methylene blue (MB), rhodamine B (RhB), and methyl orange (MO) under sunlight irradiation. The results reveal that the photocatalytic degradation efficiency of ZnO/CuO nanocomposite has been found higher than with ZnO and CuO nanoparticles for all the dyes. Also, all the synthesized nanomaterials indicate higher photocatalytic degradation efficiency for methylene blue dye among all three dyes. The kinetics of photodegradation of all the dye solutions has also been investigated in the presence of ZnO, CuO, and ZnO/CuO photocatalysts separately. The results exhibit that rate constant values for all the dyes are higher with ZnO/CuO nanocomposite than with ZnO and CuO nanoparticles. ZnO/CuO nanocomposite demonstrates degradation efficiency for MB dye 99.13%, for RhB 80.21%, and for MO 67.22% after 180 min of sunlight exposure. ZnO/CuO nanocomposite and ZnO and CuO nanoparticles also show the best reusability and stability up to three cycles for photocatalytic degradation of MB dyes among all the dyes. Therefore, green synthesized ZnO/CuO nanocomposite could be used as an efficient photocatalyst for the degradation of various toxic dyes. The mineralization of different dyes using ZnO/CuO nanocomposite has been examined by FTIR analysis. Furthermore, the mineralization of MB dye has been done by total organic carbon (TOC) measurements. [ABSTRACT FROM AUTHOR]

In the present study, we have synthesized magnesium oxide (MgO) nanoparticles by a facile and cost-effective chemical co-precipitation method with annealing at three different temperatures (350°C, 450°C, and 550°C) for the removal of various organic dyes. X-ray diffraction studies revealed that the prepared samples are having sizes below 20 nm and with pure phase. Phase transformation of hexagonal Mg(OH)2 nanoparticles to discretely cubical structured MgO nanoparticles has been observed with increasing the annealing temperatures which is also supported by the TGA/DSC analysis. Mg–O stretching vibration peaks in the range of 400–800 cm−1 obtained by FTIR spectroscopy support the formation of MgO nanoparticles. The observed Raman active bands for the annealed sample at 550°C confirm the formation of the nanocrystalline phase since these bands are typically absent in the bulk MgO as well as in Mg(OH)2. The surface morphology of the as-prepared Mg(OH)2 are aggregated nano-petals which changed into spherical shape for MgO annealed at 550°C as studied by field emission scanning electron microscopy (FESEM). The specific surface area of MgO nanoparticles annealed at 550°C using BET isotherms is found to be 37.487 m2g−1. The optical bandgaps of the prepared samples are found to be in the range of 4.4 to 5.1 eV using the Tauc plot. Adsorption studies with a variation of initial brilliant green dye concentration and contact time are carried out along with the studies of adsorption kinetic and isotherm models. Langmuir isotherm model is the most suitable model on the basis of correlation constant with maximum BG dye adsorption capacity onto MgO@550°C which is found to be 63.9 mg/g. The adsorption kinetics followed the pseudo-second-order model. Also prepared pristine MgO nanoparticles showed significant photocatalytic performance for the degradation of various dyes; brilliant green (BG: 88.91%), methylene blue (MB: 79.05%), crystal violet (CV: 76.49%), methyl orange (MO: 68.62%), and brilliant blue (BB: 40.44%) under visible irradiation. MgO nanoparticles could be a promising adsorbent and photocatalyst that may be employed in the treatment of effluents from industries. [ABSTRACT FROM AUTHOR]

The discharge of organic dye pollutants in natural water bodies has put forward a big challenge of providing clean water to a large part of the population. As the population is increasing with time, only underground water is not sufficient to complete the water requirements of everyone everywhere. Purification of wastewater and its reuse is the only way to fulfill the water needs. Nanotechnology has been used very efficiently for wastewater treatment via photocatalytic degradation of dye molecules. In the past few years, a lot of investigations have been done to enhance the photocatalytic activity of metal oxide semiconductors for water purification. In this review, we have discussed the different methods of synthesis of various metal oxide semiconductor nanoparticles, energy band gap, their role as efficient photocatalysts, radiations used for photocatalytic reactions, and their degradation efficiency to degrade the dye pollutants. We have also discussed the nanocomposites of metal oxide with graphene. These nanocomposites have been utilized as the efficient photocatalyst due to unique characteristics of graphene such as extended range of light absorption, separation of charges, and high capacity of adsorption of the dye pollutants. [ABSTRACT FROM AUTHOR]

In this work, Fe3O4/CoNi-MOF was synthesized by a simple solvothermal method. The catalytic performance of 0.2-Fe3O4/CoNi-MOF toward PMS activation was studied by degradation of 20 mg/L methylene blue (MB). The results indicated that 0.2-Fe3O4/CoNi-MOF had good catalytic ability, the removal rate of MB was 99.4% within 60 min with 125 mg/L PMS and 150 mg/L catalyst. Quenching experiment and electron paramagnetic resonance (EPR) analysis revealed that the singlet oxygen (1O2), superoxide radical (•O2−) and sulfate radical (SO4•−) played a crucial role in the catalytic degradation process. Meantime, mechanism of PMS activation by 0.2-Fe3O4/CoNi-MOF was proposed, the electrons donated by Fe2+ can also enhance the Co–Ni cycles. In conclusion, Fe3O4/CoNi-MOF composite catalyst has the advantages of simple preparation, excellent catalytic activity and reusability, which is an effective catalyst for water pollution control. [ABSTRACT FROM AUTHOR]

It is a great challenge to develop photocatalysts for the degradation of organic pollutants in the aqueous environment, especially those with excellent catalytic performance under visible light conditions. In this work, using graphene oxide (GO) as an electron shuttle agent and carrier, a hybrid of ZIF-8/NH2-MIL-125(Ti) and GO (ZIF-8/NH2-MIL-125(Ti)/GO) was prepared by a simple two-step solvothermal method. The morphology, structure, and combination of the synthesized catalysts were studied. The results showed that graphene oxide and ZIF-8 formed an in situ load on NH2-MIL-125(Ti). The construction of hybrid materials significantly improved the catalytic activity of NH2-MIL-125(Ti) in the visible light range. The degradation activity of the synthesized catalyst was further tested with reactive red dye. The results showed that the catalyst exhibited excellent catalytic removal efficiency for active red, with a degradation rate of 99.8% within 2 h. The prepared hybrid materials have good application prospects in the field of organic pollutant treatment in water. [ABSTRACT FROM AUTHOR]

In this paper, we present the first attempt to evaluate the role of carboxymethyl cellulose (CMC) as a chelating agent in the sol–gel auto-combustion method of producing barium hexaferrite (BaFe12O19). We also report the application of the system as a photocatalyst for dye degradation. The formation, morphology, and crystalline structure of the synthesized nanoparticles are determined using XRD, SEM, EDS, VSM, FTIR, and TEM techniques. High efficiency under visible light, with a band gap of 1.62 eV and a BET surface of 17.93 m2/g, has been observed for the BaFe12O19 catalyst. The operating parameters, such as reaction time, initial dye concentration, light intensity, reusability, and dye type, are studied. Degradation rates as high as 98.26% (Kapp = 0.082 min–1) and 89.07% (Kapp = 0.0743 min–1) were obtained for cases of methylene blue and malachite green under conditions of visible light irradiations when BaFe12O19 was used. The BaFe12O19 catalyst has been shown to exhibit a high degradation performance for cationic dyes. Furthermore, BaFe12O19 magnetic nanoparticles show excellent reusability for dye degradation because the photocatalyst did not exhibit a significant decrease in its activity even after five runs (81.56%). As a result, the current study confirmed that photocatalytic degradation was a promising technology for saving water and treating wastewater formed from textile dye industries. The technique can be used to study the efficiency of photocatalytic degradation and understand the process of recycling waste effluents under conditions of minimized water use. [ABSTRACT FROM AUTHOR]

Aquatic ecology has been greatly threatened by the discharge of effluents of textile and antibiotic industries into natural waters. Herein, an efficient and easily recycled reduced graphene oxide/zirconium oxide nanocomposite has been synthesized using banana peel extract (abbreviated as rGO–ZrO2 in this work). The X-ray diffraction (XRD), field emission scanning electronic microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), Brunauer–Emmett–Teller (BET), UV–visible diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared (FTIR) spectroscopy were used to analyze the synthesized material. The as-prepared rGO-ZrO2 nanocomposite was employed as a photocatalyst for the decomposition of rhodamine blue (RhB) and crystal violet (CV) dyes, and ciprofloxacin (CIP) antibiotic by illumination with direct sunlight. The RhB and CV were degraded to maximum extent of around 86 and 90%, respectively, over the rGO–ZrO2 nanocomposite after exposure to direct sunlight for 120 min. On the other hand, the degradation of CIP was approximately 93.1% over the rGO–ZrO2 nanocomposite in 240 min under same experimental conditions. Further studies were performed regarding the role of parameters like pH, catalyst dose, and scavengers, in order to understand the superiority of rGO-ZrO2 nanocomposite in degrading organic pollutants. Moreover, the intermediate products and plausible CIP degradation mechanisms were examined using liquid chromatography-mass spectrometry (LC–MS). Moreover, the catalyst was easily separated from the solution and demonstrated good stability and reusability. The RhB, CV, and CIP removal efficiency were 80%, 83%, and 88%, respectively, after five cycles. [ABSTRACT FROM AUTHOR]

A large amount of pharmaceutical industry waste (PIW) was inevitably produced every year, and the PIW can be degraded by high temperature reaction to form porous structures. The study proposed an innovative pathway to valorize PIW with hydrothermal carbonization (HTC) coupled with alkali etching (AE). Without adding any additives, magnetic hydrochar could be generated with rough surface topography and suitable specific surface area (SBET) by this method. Effects of HTC conditions and alkaline solution concentrations on the physicochemical and adsorption properties of PIW were investigated, and adsorption mechanism was explored. Based on evaluations of the magnetism, cyclic regeneration, and heavy metal leaching properties of the products, the feasibility of preparing magnetic adsorbents with solid waste by HTC coupled AE was established. The alkaline etching pharmaceutical industry waste (AEPIW) hydrochar showed the highest SBET (54.64 m2/g) after the PIW was treated by 260 °C for 2 h plus 1 mol/L KOH. The removal rate of methylene blue (MB) could exceed 90% and the saturated magnetization was ~8 emu/g. The proposed new method was able to convert the low-value solid industrial waste into high-performance hydrochar-based magnetic adsorbents, which was tested to have a capability to efficiently and sustainably remove organic pollutants from water. [ABSTRACT FROM AUTHOR]

Discharge of the untreated dye-containing wastewaters will induce water source pollution and further harm aquatic organisms. In this study, the akaganéite/polyaniline catalyst (β-FeOOH/PANI, about 1.0 μm) could be successfully composed by polyaniline (PANI, (C6H7N)n, 200–300 nm) and akaganéite (β-FeOOH, FeO(OH)1−xClx, less than 200 nm), according to the identification and characterization results of XRD, Ramon, FTIR, XPS, SEAD, EDS, and FESEM (or HRTEM). Due to PANI providing more photogenerated electrons, the β-FeOOH/PANI composite (compared with β-FeOOH) in photo-Fenton system had the more highly catalytic degradation capacity to Acid Orange II (AOII) under an optimal condition (7.5 mmol/L of H2O2 oxidant, 40 mg/L of AOII, 0.2 g/L of catalyst dosage, and pH 4.0). The AOII degradation kinetics could be well fitted by pseudo-first-order model. In photo-Fenton catalytic process of AOII dye, the ∙OH and h+ were the main reaction substances. The AOII in solutions could be gradually mineralized into non-toxic inorganic H2O molecule and CO2. The β-FeOOH/PANI catalyst also had a good reusable ability of about 91.4% AOII degradation after 4 runs. These results can provide a reference for synthesis of catalyst used in photo-Fenton system and the applications in degradation removal of organic dye from wastewaters. [ABSTRACT FROM AUTHOR]

Herein, a novel nanocomposite, namely, Zn-modified CeO2@biochar (Zn/CeO2@BC), is synthesized via facile one-step sol-precipitation to study its photocatalytic activity towards the removal of methylene blue dye. Firstly, Zn/Ce(OH)4@biochar was precipitated by adding sodium hydroxide to cerium salt precursor; then, the composite was calcined in a muffle furnace to convert Ce(OH)4 into CeO2. The crystallite structure, topographical and morphological properties, chemical compositions, and specific surface area of the synthesized nanocomposite are characterized by XRD, SEM, TEM, XPS, EDS, and BET analysis. The nearly spherical Zn/CeO2@BC nanocomposite has an average particle size of 27.05 nm and a specific surface area of 141.59 m2/g. All the tests showed the agglomeration of Zn nanoparticles over the CeO2@biochar matrix. The synthesized nanocomposite showed remarkable photocatalytic activity towards removing methylene blue, an organic dye commonly found in industrial effluents. The kinetics and mechanism of Fenton-activated dye degradation were studied. The nanocomposite exhibited the highest degradation efficiency of 98.24% under direct solar irradiation of 90 min, at an optimum dosage of 0.2 g l−1 catalyst and 10 ppm dye concentration, in the presence of 25% (V/V) 0.2 ml (4 µl/ml) hydrogen peroxide. The hydroxyl radical generated from H2O2 during the photo-Fenton reaction process was attributed to the nanocomposite's improved photodegradation performance. The degradation process followed pseudo-first-order kinetics having a rate constant (k) value of 0.0274 min−1. [ABSTRACT FROM AUTHOR]

This study presents the results of synthesis and characterization of nanoparticles of cobalt ferrite (CoFe2O4) and nickel ferrite (NiFe2O4) using co-precipitation method followed by application for removal of hazardous organic textile dyes of thiazole yellow G (TYG) and alizarin yellow R (AYR). XRD analysis confirmed formation of cubic spinel structure with average crystallite sizes at 16.07 nm and 13.84 nm for CoFe2O4 and NiFe2O4, respectively. Field emission scanning electron microscopy (FESEM) analysis showed agglomeration of spherical shape morphology with uniformly distributed Co, Ni, Fe, and O elements. The surface area calculated from Brunauer–Emmett–Teller (BET) analysis was 64 m2/g and 62 m2/g for CoFe2O4 and NiFe2O4, respectively. Vibrating sample magnetometer (VSM) showed super-paramagnetic behavior for all samples with magnetic saturation (Ms) at 7.269 and 6.61 emu/g for CoFe2O4 and NiFe2O4, respectively. The adsorption influencing parameters such as pH of solution, quantity of adsorbent, and contact time on dye removal efficiency were thoroughly investigated. Overall, acidic condition of samples with pH at 4 favored the maximum removal efficiency by CoFe2O4 as 98, 97, and 93%, and by NiFe2O4 as 96, 93, and 92%, respectively, for TYG, AYR, and mixture sample. The Langmuir adsorption isotherm model describes the equilibrium of all samples with the best fit of coefficient of determination (R2). The adsorption results fitted well with a pseudo-second-order kinetic model for all samples. The regeneration-reuse ability of adsorbents and cost estimation analysis of the dye removal process suggested that the economic suitability of nano-adsorbents for remediation of textile effluents was favored. The estimated thermodynamic parameters inferred that the removal of organic dyes onto the surface of CoFe2O4 and NiFe2O4 is a spontaneous, favorable, and exothermic physical adsorption process. [ABSTRACT FROM AUTHOR]

Graphene, a 2D single-layered carbon sp2 hybrid substance set in a honeycomb network, is widespread in many carbon-based materials. Due to its extraordinary optical, electrical, thermal, mechanical, and magnetic competences as well as its significant specific surface area, it has attracted a lot of interest recently. Synthesizing graphene refers to any process for creating or extracting the material, depending on the desired purity, size, and efflorescence of the finished good. Numerous methods have been employed for graphene synthesis categorized as top-down procedures and bottom-up procedures. Graphene finds its implementations in various industries such as electronics, energy, chemical, transport, defence, and biomedical areas such as accurate biosensing. It has been widely used in water treatment as a binder for organic contaminants and heavy metals. Many researches have fixated on creating various modified graphene, graphene oxide composites, graphene nanoparticle composites and semiconductor hybrids of graphene for contaminant removal from water. In this review, we have tried to address various production methods for graphene and its composites along with their advantages and disadvantages. Furthermore, we have presented a summary on graphene's outstanding immobilization of a variety of contaminants like toxic heavy metals, organic dyes, inorganic pollutants and pharmaceutical wastes. Additionally, a development of graphene-based microbial fuel cell (MFC) has been evaluated in an effort to produce ecological wastewater treatment and bioelectricity. [ABSTRACT FROM AUTHOR]

Herein, a highly porous bimetal–organic framework (bi-MOF) based on cobalt and nickel was successfully in situ grown on organoclay (OC) clusters by solvothermal method. Accordingly, the hierarchical porous CoNi-MOF/OC composite with a superior specific surface area of 2046 m2/g and a large pore volume of 0.763 cm3/g was obtained, which facilitated the adsorption of organic dyes. A morphological study using scanning electron microscopy indicated the formation of uniform bi-MOF crystals on the OC plates. Furthermore, the single- and multi-dye adsorption assays were implemented to precisely evaluate the adsorption capacity and selectivity of CoNi-MOF/OC composite to anionic and cationic dyes. The results revealed a high adsorption capacity of 58.61 mg/g at an adsorbent content of 15 mg, initial dye concentration of 20 ppm, and contact time of 25 min for MB, which is superior to several existing clay-based adsorbents. The adsorption kinetics study showed that the adsorption of cationic and anionic dyes onto the CoNi-MOF/OC composite followed the pseudo-second-order kinetic model. Interestingly, the regeneration study showed appropriate reusability and stability of the CoNi-MOF/OC composite for the removal of organic dyes with an almost unchanged structure after four regeneration cycles. The results of this study provide new insights for the rational design and fabrication of next-generation clay-based adsorbent by combining the synergistic advantages of bi-MOF with superior specific surface area and pore volume with organoclay composition and structure. [ABSTRACT FROM AUTHOR]

Herein we report multifunctional surface-modified CuO nanomaterials were used to fulfill escalating needs in the electrochemical energy storage system and to achieve efficient photocatalysts for the degradation of AR88 organic dye. Due to the atom economy, ease of synthesis, high capacitance, observable electrochemical responsiveness, and low bandgap in CuO-based nanomaterials, its active surface was modified through cationic surfactant CTAB. Surface-modified nanoparticles were characterized using various characterization techniques such as XRD, DRS, FESEM, and TEM. Intriguingly the synthesized materials demonstrated a capacitance of 133 F/g with a long-term charge–discharge cycle of 2000 cycles. In addition, at pH 11, the material also exhibited a superior dye degradation performance under the UV lamp by showing 94.8% AR88 degradation at a catalyst concentration of 1.0 g/L. Hence, we believe this concept would provide novel insights into the preparation of the simplest and cheaper multifunctional materials for next-generation energy storage and photocatalytic applications. [ABSTRACT FROM AUTHOR]

Textile industries are one of the leading environmental pollutants by releasing harmful dye effluents. In many textile distrts, the amount of excess color in treated textile effluent that exceeds regulatory limitations is still being a major concern. The combining usage of nanomaterials and polymer material to solve these issues using various techniques. In this research, graphene oxide–copper oxide (GO–CuO) nanomaterial have been incorporated into cellulose-acetate (CA), poly-ether sulfone (PES) blend polymer by using phase inversion process to fabricate thin film nanocomposite (TFN) membrane for removal of dye pollutant. The physiochemical properties of prepared TFN materials were studied by Fourier transform infra-red spectroscopy (FT-IR), X-ray diffractometer (XRD), field emission scanning electron microscopy (FE-SEM), atomic force microscopy (AFM), thermo gravimetric analysis (TGA), and mechanical strength analysis. Dye adsorption experiments were performed with four typical water-soluble organic dyes methylene blue (MB), rhodamine blue (Rh. B), methyl orange (MO) and Congo red (CR). After reaching adsorption equilibrium, the composite membrane final removal effectiveness for MB 92.42%, Rh. B 89.39%, CR 68.39%, and MO 58.82% respectively. As a result, the fabricated TFN material proves to be an effective adsorbent material for cationic dye molecules. Also, when the fabricated material was tested with textile industry effluent sample, all physio-chemical properties exhibited a considerable decrease in concentrations when compared to the real textile effluent concentration. The treated effluents permitted for a relatively greater growth and germination index of Tropical amaranth roots than the textile effluent, this demonstrates that phytotoxicity testing was also successful. The most effective temperature, concentration and pH were found to be 273 K, 1 × 10−5 M and pH 9. The fabricated TFN membrane material (GO–CuO @ CA–PES) can be recommended for water treatment applications. [ABSTRACT FROM AUTHOR]

Tetracycline (TC) is a frequently administered antibiotic in many countries, due to its low price and excellent potency. However, certain antibiotics can be hazardous to living creatures due to their accumulation by complexation with metal ions which can contribute to teratogenicity and carcinogenicity. In this investigation, copper oxide-ferric oxide nanocomposite (CuO/Fe2O3 nanocomposite) was synthesized employing Psidium guajava (P. guajava) leaf extract as a reductant as well as a capping agent in an environment friendly and economical green synthesis method. The as-synthesized CuO/Fe2O3 nanocomposite was comprehensively characterized using various sophisticated techniques and its efficiency as a photocatalyst for degradation of tetracycline (TC) antibiotic and toxic dyes, i.e., rhodamine B (RhB) and methylene blue (MB) were investigated. The CuO/Fe2O3 nanocomposite exhibited exceptional efficiency for degradation of TC antibiotic (88% removal in 80 min), RhB (96% removal in 40 min), and MB (93% elimination in 40 min) with apparent rate constant of 0.048, 0.068, and 0.032 min–1, respectively. In the degradation experiments, photocatalytic activity of CuO/Fe2O3 nanocomposite was studied by varying different factors such as time of contact, catalyst dose, and solution pH. The role of reactive species in antibiotics and dye degradation was validated by radical scavenging studies which indicated that.OH radical played a critical role in photocatalytic decomposition. Furthermore, liquid chromatography-mass spectrometry (LC–MS) investigations were employed to anticipate a plausible mechanism for TC degradation. [ABSTRACT FROM AUTHOR]

By integrating the benefits of poly vinyl alcohol (PVA) and chitosan (CS) with α-MnO2 nanoparticles (MNPs), a novel type of nano-polymer composite (PVA/CS-MNP) membrane was synthesized through a simple and facile casting method. In this proposed work, the membrane prepared was used for removal of organic textile dyes from their aqueous solutions. The as-synthesized PVA/CS-MNP membrane was examined using different analytical techniques such as Fourier transform infrared spectroscopy (FTIR) and field emission scanning electron microscopy (FESEM), and mechanical properties of material was also studied. Two cationic dyes, methylene blue (MB) and eosin yellow (EY), were chosen as template dyes to be removed from industrial waste water. These dyes were degraded by carrying out a reaction in which the synthesized membrane was used as a photocatalyst. The study of kinetics revealed that the reaction process followed pseudo-first-order kinetics. The efficiency of catalyst and the rate of reaction were also examined by varying parameters such as pH, initial concentration of dyes, and composition of membrane. The maximum efficiency of catalyst was observed at pH 12 as more than 95% of dyes degraded within 1 h of time span. The catalyst was found to be reusable as its efficiency did not deteriorate even after using it for several times. Such functional membrane having higher stability, low production cost, excellent efficiency to degrade dyes, and good recyclability are promising material for distinctly effective deletion of organic dyes from waste water. [ABSTRACT FROM AUTHOR]

In this study, a series of ternary composite photocatalysts ZnO/g-C3N4/AgCl(x) (x is the amount of AgCl added, x=0.05, 0.1, 0.15 g) were synthesized, and various characterization methods were used to analyze the morphology, structural, and photochemical properties of the above samples. The photocatalytic activity of the obtained samples was evaluated by degrading rhodamine B (RhB) and acid orange (AOII) under xenon lamp irradiation. The results show that the degradation rate of ZnO/g-C3N4/AgCl (0.1 g) is 99% within 60 min, which is much higher than the 38% degradation rate of g-C3N4. After five cycles, the degradation efficiency of RhB and AOII by ZnO/g-C3N4/AgCl (0.1 g) were still 85% and 94%, respectively. In addition to colored dyes, the photocatalytic degradation of colorless tetracycline hydrochloride (TCH) compounds was also investigated to understand the effect of photosensitization on the degradation process. Based on the electronic structure analysis of the DFT calculations, a staggered heterojunction structure was found between g-C3N4, ZnO, and AgCl. The enhanced photocatalytic activity of the ternary composite is mainly attributed to the efficient separation of charge carriers through the synergistic removal of photogenerated electrons in g-C3N4 by ZnO and AgCl. Radical trapping experiments confirmed that •O2− and h+ were the main active species in the reaction system. As a visible light-responsive catalyst, ZnO/g-C3N4/AgCl can be effectively applied to the degradation of organic dye pollutants and has broad application prospects. [ABSTRACT FROM AUTHOR]

In this work, Ti-doped Fe2O3 with hollow ellipsoidal capsules nanostructure has been prepared in a green manner using plant extract (flax seed). This new green hematite nanomaterial has been evaluated as photocatalyst for water treatment by testing its activity for degradation of bromophenol blue dye (BPB) and 2,4-dichlorophenoxy acetic acid (2,4-D) herbicide. For a better understanding of the green material properties, a comparison with the pristine Fe2O3 nanospheres previously prepared by the same procedure is included. Structural and optical properties of the green prepared materials are studied. The results revealed the success doping of Ti4+ at Fe3+ site, without forming any of TiO2 phases. It was also found that the Ti doping resulted in the reduction of the band gap of Fe2O3 as well as changing the morphology. The Ti-doped Fe2O3 nanomaterial exhibited an enhanced photocatalytic activity either for BPB dye or for 2,4-D degradation with more than 2 times higher rate than that using pristine Fe2O3. [ABSTRACT FROM AUTHOR]

The efficient and rapid removal of organic dyes from wastewater remains a complex and challenging task. In this study, UiO-66-NH2 was prepared by solvothermal synthesis, and then, UiO-66-NS was prepared by compounding l-cysteine with UiO-66-NH2 via the Ugi reaction for the efficient removal of methyl orange. UiO-66-NS was prepared by the addition of 1 mmol l-cysteine and showed good adsorption of methyl orange with 92.00% removal. Pseudo-second-order kinetics and Langmuir isotherms more accurately described the adsorption process of UiO-66-NS on methyl orange, which indicated that the adsorption process was dominated by monolayer adsorption of chemical reactions, and the maximum adsorption amounts of UiO-66-NS on methyl orange were 242.72 mg/g at 298 K. In addition, UiO-66-NS exhibited ultrahigh stability in acidic, neutral, and alkaline media (pH = 3–10), but its adsorption of methyl orange after 5 cycles was only 59.53% of the maximum adsorption amount. The adsorption mechanism is primarily electrostatic adsorption of UiO-66-NS with methyl orange, hydrogen bonding, and π-π interactions. This atomically economical Ugi multicomponent reaction provides new ideas for the preparation of structurally designable adsorbents with excellent performance. [ABSTRACT FROM AUTHOR]

In this research, the treatment of methylene blue (MB) dye wastewater by a novel system that combines H2O2 with an aluminum-carbon micro-electrolysis (ACE) was explored. The effects of the H2O2 amount, initial pH, aluminum to carbon ratio, total aluminum-carbon mass, dye concentration, and reaction temperature on degradation of MB were investigated. The findings revealed that under the following conditions: H2O2 34.0 mg/L, initial pH of 3.0, aluminum-to-carbon ratio of 2:1, total aluminum-carbon mass of 2.0 g/L, MB concentration of 20 mg/L, and 20 °C, the degradation rate of MB could reach 99.3% after 180 min, which is 18.4% more compared with ACE at the same conditions without H2O2. Through the quenching experiments, it was proved that the efficient free radicals produced during degradation are •OH and •O2-. Finally, a possible mechanism of H2O2 enhanced aluminum carbon micro-electrolysis (HP-ACE) for MB degradation was discussed. [ABSTRACT FROM AUTHOR]

In our present study, the photocatalytic degradation of malachite green (MG) an organic dye was carried out using a phycocyanin extract of Spirulina platensis under the irradiation of sunlight. The aim of the present study is to incorporate a simple, novel, an eco-friendly, and cost-effective degradation of dyes without using any harmful metals and chemicals. It was observed that 25 ppm of MG dye got degraded nearly to 100 % at 3 h. The UV absorbance studies indicate the absence of a peak at 620 nm which is a conclusive evidence for MG dye degradation. An optimization study of MG dye degradation was evaluated by Response Surface Methodology using Minitab module 20.4.0.0 statistical software and its percentage of degradation was statistically analyzed using analystat. The FT-IR studies of raw spectra show minimal variation; however, the deconvoluted spectra in the region of 1600–1700 cm−1 indicate the variation in the secondary structure of amide I bands that leads to the dye degradation. The dye degradation study mainly follows the first-order kinetics between the time intervals of 60–180 min. The characteristics of degraded water were assessed by a TOC analyzer. The value of total inorganic carbon (TIC) in MG before treatment was 90 mg/L and seems to be slightly high when compared to MG after treatment which was found to be 87.65 mg/L and the adsorbent-treated water with a low value of 54.25 mg/L. These results well matched with the characteristics of normal water. The presence of phycocyanin in the degraded water was effectively removed by treating with activated carbon and it was confirmed with fluorescence analysis. These results support that the MG dye degradation was exhibited by phycocyanin extract and bio-mimics the quantum dot photocatalytic activity. [ABSTRACT FROM AUTHOR]

This study deals with the toxicity of the treated solutions of two types of dyes, namely, the anthraquinonic Reactive Bleu 19 dye (RB19) and the bi-azoic Direct Red 227 dye (DR227), which are treated in single and binary mixture systems. The target molecules were removed by the photocatalysis process using ZnO as a catalyst, which was calcined at two temperatures 250 and 420 °C (ZnO250 and ZnO420) prepared in the lab by the one-step calcination method. XRD, TEM, EDX, XPS, FT-IR, BET, RAMAN, and EPR analyses were carried out to characterize the catalyst material. While the phytotoxicity was being conducted using watercress seeds, the cytotoxicity took place using a cell line (raw) and an intestinal cell (caco-2). The XRD analysis showed the partial calcination of ZnO250 and the presence of anhydrous zinc acetate along with the ZnO nanoparticles (NPs). This result was not observed for ZnO420. Despite the complete discoloration (100%) of all the final solutions, ZnO250 exhibited a high cytotoxicity and phytotoxicity against the RB19 dye after the photocatalytic treatment; however, it was not the case of ZnO420 which was selected as an eco-friendly photocatalyst for the degradation of organic dyes based on the results of removal efficiency, cytotoxicity, and phytotoxicity. [ABSTRACT FROM AUTHOR]

Excessive discharge of toxic dyes is detrimental to ecological system and human health. Therefore, an effective photocatalyst must be designed and developed to degrade dyes from wastewater. Herein, a novel one-dimensional (1D) flower-like recoverable ZnFe2O4/C/MnO2/BiOI magnetic composite photocatalyst was synthesized via electrospinning technique combined with hydrothermal method. The photocatalytic activities of composite photocatalyst were evaluated by degrading methyl orange (MO) and Rhodamine B (RhB) under simulated light irradiation. The efficiency of ZnFe2O4/C/MnO2/BiOI photocatalyst in visible light for 150 min reached 91% (MO) and 120 min reached 94% (RhB). Moreover, the degradation rate of MO still remained 78% after five cycles. The design of 1D magnetic flower-like composite provided a new strategy for preparing photocatalysts possessing excellent photocatalytic efficiency and cyclic stability. [ABSTRACT FROM AUTHOR]

The photocatalytic activity of semiconducting silver carbonate was restricted by the lower stability and fast recombination rate of photogenerated electron–hole pairs. Sulfur-doped graphene oxide (SGO) is used as a cocatalyst for improving the photocatalytic activity of Ag2CO3 by reducing the recombination rate. A simple precipitation method was used for the modification of silver carbonate. The chemical, physical, optical, and electrochemical properties of the modified photocatalyst was characterized by XRD, SEM, TEM, UV–vis DRS, XPS, CV, impedance, and amperometry. The fabricated SGO-Ag2CO3 composite was successfully degraded various organic pollutants such as methylene blue (MB), rhodamine B(RhB), methyl orange (MO), tartrazine, and thiram with augmented mineralization. The optimization of weight percentage of the developed binary composite with 0.5% SGO-Ag2CO3 showed enhanced photocatalytic degradation and followed pseudo-first-order kinetics with rate constant 0.126. More than 90% of degradation efficiency of the pollutants within a short time promises the binary heterostructure for future industrial applications. The excellent stability and reproducibility of the composite opened a new route in the treatment of wastewater. [ABSTRACT FROM AUTHOR]

Water pollution caused by the discharged insolubility petroleum contaminants and organic compound dyes seriously threatens the natural self-purity capacity of the water body and the survival of aquatic species, so it is imperative to restraint the deterioration of the aquatic environment. In this paper, pathways are propounded for the simultaneous removal of insoluble spilling oil and organic dye contaminants. Particularly, hydrophobic ZnSnO3 after stearic acid modification and Bi2MoO6 photocatalysts are introduced into the cotton fabric substrate through solution dip-coating. The durability of the prepared fabric suffers from the acid–base corrosion, thermal treatment and mechanical wear, while still exhibiting remarkable water-repellent (WCA > 150°) property. Furthermore, the remarkable photocatalytic activity makes it possible for reusable degradation and the primary active species, namely the holes, to be verified by the radicals-capturing experiment. It is worth observing that as-prepared superhydrophobic fabric possesses admirable water-proof property and cycling durability of decomposing toxic water-soluble organic dye, thereby contributing to further realizing the ecological concept of clear waters. [ABSTRACT FROM AUTHOR]

Since the advent of photocatalytic degradation technology, it has brought new vitality to the environmental governance and the response to the energy crisis. Photocatalysts harvest optical energy to drive chemical reactions, which means people can use solar energy to complete some resource-consuming activities by photocatalysts, such as environmental governance. In recent years, researchers have tried to combine photocatalyst TiO2 with building materials to purify urban air and obtained good results. One of the important functions of photocatalysts is to degrade organic pollutants in water through light energy, but this technology has not been reported in the practical application areas. To extend this technology to practical application areas, photocatalytic concrete for degrading pollutants in waters was proposed and demonstrated for the first time in this paper. The photocatalytic concrete proposed based on the K-g-C3N4 shows a strong ability to degrade the organic dyes. According to the experiment results, the angle of light source plays an important role in the process of photocatalytic degradation, while waters with pH value of 6.5–8.5 hardly influenced the degradation of organic dyes. When the angle of light source is advantageous for photocatalytic concrete to absorb more visible light, more organic dyes will be degraded by photocatalytic concrete. The degradation rate of methylene blue could reach about 80% in ½ hour under desirable conditions and is satisfied compared with that of reported works. This study implicates that photocatalytic concrete can effectively degrade organic dyes in water. The influences of changes in the water environment hardly affect the degradation of organic pollutants, which means photocatalytic concrete can be widely used in green infrastructures to achieve urban sewage treatment. [ABSTRACT FROM AUTHOR]

Undoped and manganese doped ZnS nanocrystals encapsulated with thioglycolic acid (ZnS-TGA) were synthesized and characterized with different techniques, and finally tested in the photodegradation of a methyl orange in aqueous solution under UV and sunlight irradiations. FTIR and X-ray diffraction results confirmed the functionalization of these nanocrystal surface by thioglycolic acid and the formation of crystalline structures of ZnS and Mn-doped ZnS with cubic and hexagonal phases. Calculated average size of ZnS nanocrystals was in the range of 2–3 nm. It was observed a blue shift of the absorbance threshold and the estimated bandgap energies were higher than that of Bulk ZnS thus confirming the quantum confinement effect of charge carriers. Photoluminescence spectra of ZnS nanocrystals exhibited emission in the range of 410–490 nm and the appearance of an additional emission band around 580 nm (2.13 eV) connected to the 4T1 → 6A1 transition of the Mn2+ions. Photodegradation of methylene orange with undoped and Mn-doped ZnS-TGA nanocrystals was investigated. Dye adsorption prior to photocatalysis using nanocrystals was studied via kinetic and equilibrium experiments. The maximum dye adsorption capacity on doped ZnS-TGA was ~ 26.98 mg/g. The adsorption kinetic was found to follow the pseudo-second-order kinetic model. A statistical physics model was used to analyze the equilibrium data where the calculated adsorption energy was 17–18 kJ/mol. It was concluded that the dye adsorption was associated to the hydrogen interaction where the removal process was feasible and multi-molecular at 25 °C. The photocatalytic activity of undoped ZnS nanoparticles under UV irradiation showed better efficiency than doped nanocrystals thus indicating that manganese doping generated a dropping of the photocatalytic degradation of the dye. Dye degradation efficiency of 81.37% using ZnS-TGA nanocrystals was achieved after 6 min, which indicated that ZnMnS-TGA nanocrystals may be considered an alternative low cost and environmental friendly material for facing water pollution caused by organic compounds via photodegradation processes. [ABSTRACT FROM AUTHOR]

In order to improve the treatment efficiency of printing and dyeing wastewater, the carbon nanotubes-silver-modified-titanium dioxide (CNTs-Ag-TiO2, CAT) ternary composite was prepared by a mechanical mixing method. It was found that the morphology of the prepared CAT sample was uniformly coated with strips of CNTs, speckled Ag, and lumpy TiO2. The (002) crystal plane of CNTs, the (101) crystal plane of TiO2, and the (111) crystal plane of Ag were observed, which possessed functional groups such as Ti-OH and Ti-O-C, indicating that the prepared CAT sample had photocatalytic reaction sites. The visible light utilization of titanium dioxide can be improved. The treatment effect of different proportions of CNTs-Ag-TiO2 on Congo red wastewater was tested, and the results showed that the optimum degradation effect of Congo red wastewater was CNTs: Ag = 10:1, and the doped amount of CNTs/Ag was 15%, and the removal rate of Congo red wastewater could reach 100% within 140 min. The excellent removal effect of CAT ternary composite on Congo red wastewater provided a new idea and way for the modification of TiO2 and its composites for the potential of organic dyes degradation. [ABSTRACT FROM AUTHOR]

The reduced graphene oxide dopped equaixial geometry TiO2 (rGO/egTiO2) composite as photocatalyst was synthesized hydrothermally with various mass ratios of tetrabutyl titanate. The photocatalyst is considered to be rGO/equaixial geometry TiO2 in terms of modifying the combined reduced graphene Oxide and TiO2. The rGO plays a vital role in rGO/egTiO2 composite as photocatalysts were analyzed in methylene blue (MB) and rhodamine B (RhB) photocatalytic degradation under UV and simulated solar light irradiation. This synthesized catalyst was characterized by various analytical techniques such as XPS, XRD, SEM, BET, and TEM. The rGO/egTiO2 composite exhibits enhanced photocatalytic performance with degradation rates of 97.5 and 97% on RhB and MB for 60 min under UV radiation respectively, while the degradation rate of 94 and 92 % was observed on the same dyes for 6 h under the simulated sunlight radiation. The enhanced photocatalytic performance of the rGO/egTiO2 composite under ultraviolet irradiation source was owing to a high separation efficiency of the photo-induced electron-hole pairs, while the photocatalytic performance under simulated sunlight radiation was due to the photosensitive and charge separator behavior of rGO. This offers us an excellent potential of significant photocatalytic activity for the removal of organic contaminants from wastewater. [ABSTRACT FROM AUTHOR]

Uniformly dispersed Pd nanoparticles on certain supports exhibit exceptional catalytic performance toward various environmental applications. In this work, ultrafine Pd nanoparticles anchored on CeO2 nanorods were synthesized via an absorption-in situ reduction method. The activity of the CeO2/Pd nanocomposites was systematically investigated toward reduction of 4-nitrophenol (4-NP) and organic dyes including methyl blue, rhodamine B, methyl orange, and Congo red. The results indicated that the CeO2/Pd nanocomposites with different weight ratios of Pd nanoparticles (10.23 wt%, 11.01 wt%, and 14.27 wt%) can almost completely reduce 4-NP with a rate constant of 3.31×10−1, 3.22×10−1, and 2.23×10−1 min−1. Besides, the 10.23 wt% CeO2/Pd nanocomposites exhibit remarkable enhanced catalytic activity toward reduction of organic dyes. The catalysts display ideal stability after being used for three times for the reduction of 4-NP. We believe that our strategy demonstrated here offers insights into the design and fabrication of novel Pd-based nanocomposites for various heterogeneous catalysis applications. [ABSTRACT FROM AUTHOR]