Sunlit photocatalytic degradation of organic pollutant by NiCr2O4/Bi2S3/Cr2S3 tracheid skeleton nanocomposite: Mechanism, pathway, reactive sites, genotoxicity and byproduct toxicity evaluation.

In this study, 3D C2S3 (CS) and 2D Bi2S3 (BS) modified NiCr2O4 nanocomposite (NCO-BS-CS NCs) was prepared by sonochemical assisted co-precipitation method for the enhanced photocatalytic activity. Here, NCO-BS-CS NCs showed band gap energy of 2.23 eV and the PL intensity of NCO-BS-CS NCs was lower than NCO, BS, and CS NPs. Thus, the results indicate the fabricated NCO-BS-CS NCs enhance the charge segregation and lower in recombination rate. NCO-BS-CS NCs showed enhanced photodegradation of methyl orange (MO) (95%) and congo red (CR) (99.7%) respectively. The total organic compound (TOC) analysis shows the complete mineralization of about 91 and 98% for MO and CR respectively. Furthermore, the Fukui function was used for the prediction of reactive sites in the photodegradation pathway of MO and CR by NCs. ECOSAR program was done to determine the toxicity of the intermediate and the results conclude that the degraded product shows nontoxic to the environmental organism (fish, daphnia, and algae). Thus, the fabricated NCO-BS-CS NCs can be used for the remediation of toxic organic pollutants from the waste water by photocatalytic degradation.

Green synthesis of two-electron centre based ZnO/NiCo2S4 QDs-OVs using Punica granatum fruit peel extract for an exceptional visible light photocatalytic degradation of doxycycline and ciprofloxacin.

Biosynthesis of nanomaterials using plant extract makes them attractive in the field of photocatalysis as they are environmental friendly. The current study focused on the biosynthesis of ZnO/NiCo2S4 QDs (NCs) using Punica granatum fruit peel extract as the reducing agent. The nanomaterials were characterized with XRD, FTIR, Raman, SEM, TEM, UV-vis DRS, BET, PL, EIS, and ESR analysis and were used for photocatalytic degradation of doxycycline (DOX) and ciprofloxacin (CIP). The bandgap of ZnO is 3.2 eV, and the decoration of NiCo2S4 QDs aids in narrowing the bandgap (2.8 eV), making the NCs visible light active. The fabricated NCs achieved 99 and 89% degradation of DOX and CIP respectively. The photocatalytic efficiency of ZnO/NiCo2S4 QDs was much higher compared to individual ZnO and NiCo2S4 QDs. The half-life period of DOX and CIP were evaluated to be 58 and 152 min respectively. The percentage of TOC removal in the photodegraded product of DOX and CIP was estimated to be 99 and 89% respectively, indicating the mineralization of the compounds. The enhanced photocatalytic efficiency of the NCs was attributed to the narrowed visible light active bandgap, synergistic charge transfer across the interface, and lower charge recombination. The intermediates formed during the photocatalytic degradation of DOX and CIP were analyzed using GC-MS/MS analysis, and the photodegradation pathway was elucidated. Also, the toxicity of the intermediates was computationally analyzed using ECOSAR software. The fabricated ZnO/NiCo2S4 QDs have excellent stability and reusability, confirmed by XRD and XPS analysis. The reusable efficiency of the NCs for the photocatalytic degradation of DOX and CIP were 98.93, and 99.4% respectively. Thus, the biologically fabricated NCs are shown to be an excellent photocatalyst and have wide applications in environmental remediation.

Robust visible light active CoNiO2-BiFeO3-NiS ternary nanocomposite for photo-fenton degradation of rhodamine B and methyl orange: Kinetics, degradation pathway and toxicity assessment.

Sustainable wastewater treatment is crucial to remediate the water pollutants through the development of highly efficient, low-cost and separation free photocatalyst. The aim of this study is to construct a novel CoNiO2-BiFeO3-NiS ternary nanocomposite (NCs) for the efficient degradation of organic pollutants by utilising visible light. The NCs was characterized by various physiochemical techniques, including HR-TEM, SEM, XPS, FT-IR, ESR, EIS, PL, UV-visible DRS, and N2 adsorption and desorption analysis. The photocatalyst exhibits extraordinary degradation efficiency towards MO (99.8%) and RhB (97.8%). The intermediates were determined using GC-MS analysis and the degradation pathway was elucidated. The complete mineralization was further confirmed by TOC analysis. The CoNiO2-BiFeO3-NiS ternary NCs have shown excellent photostability, structural stability and reusability even after six cycles and it is confirmed by XRD and XPS analysis. The kinetic study reveals that the photodegradation of the dyes follows first order reaction. The influence of different pH, dye concentrations and NCs dosages were investigated. The intermediate toxicity was predicted by computational stimulation using ECOSAR software. The NCs shows promising potential for ecological safety which demonstrates its practical application in the treatment of waste water pollutants in large scale.

Double Z-Scheme ZnCo2O4/MnO2/FeS2 photocatalyst with enhanced photodegradation of organic compound: Insights into mechanisms, kinetics, pathway and toxicity studies.

The present work highlights the preparation of double Z-scheme ZnCo2O4/MnO2/FeS2 nanocomposite (NCs) and investigated its photocatalytic activity against methyl orange (MO) dye degradation under visible light. An array of techniques was carried out to characterize the nanoparticles (NPs) in order to evaluate their morphological, structural, optical, and photocatalytic properties using FE-SEM, TEM, XRD, N2 adsorption and desorption studies, PL, UV-visible spectrophotometer, XPS, Raman, and UV-vis DRS analysis. The degradation efficiency of NCs was tested along with different parameter studies such as different pH, NCs concentration, dye concentration, reusability and structural stability. The NCs exhibited complete photodegradation of MO dye under visible light within 80 min at pH 4. The structural and compositional stability of the prepared NCs over 6 consecutive cycles was tested via XRD and XPS analysis. The results of active species trapping experiments showed that O2-• and OH• are responsible for the degradation of MO dye. The TOC analysis showed 95% of mineralization by the prepared NCs. The MO dye degradation pathway was determined using GC-MS/MS analysis and drafted all the intermediates involved. End product toxicity via seed germination and intermediate toxicity study using ECOSAR software results in less toxicity of end product compared to parent compound. Finally, the genotoxicity of the prepared NCs was evaluated using Allium cepa and showed its no causes of cytotoxicity & genotoxicity by the prepared NCs. ZnCo2O4/MnO2/FeS2 NCs exhibited its high photocatalytic activity and the toxicity studies confirms that there is no cause of any environmental impact.

A prominent dual heterojunction framed CuWO4/Bi2WO6/MnS ternary NCs for para-chlorophenol degradation, Cr(VI) reduction & toxicity studies.

In account of environmental remediation, an ideal photocatalyst was fabricated for the effective treatment of water systems. Herein, dual heterojunctions framed CuWO4/Bi2WO6/MnS nanocomposite (NCs) was synthesized via simple co-precipitation method followed by ultra-sonicated assisted route. The prepared NCs were investigated its photocatalytic degradation performance using para-chlorophenol (4-CP) and reduction of chromium VI (Cr (VI)) under visible light irradiation. The photocatalyst were characterized by various analytical techniques including XRD, HR-TEM, XPS, UV-vis DRS, FE-SEM, EIS, PL, ESR, Raman and N2 adsorption and desorption studies. The excellent photodegradation of 4-CP was observed within 180 min by the NCs. Similarly, the Cr (VI) reduction was about 97% within 140 min. The effect of pH and influence of different dosage of NCs and 4-CP on the photodegradation efficiency was investigated. The reusability and stability of the NCs was examined over 6 consecutive runs where the XRD and XPS confirm the structural stability of the prepared NCs. The scavenging experiment were carried out to elucidate the mechanism and the active species involved were O2-• and OH• radicals. The TOC analysis affirmed the complete mineralization of the prepared NCs. The ecotoxicity analysis was carried out to determine the toxicity effect of intermediates using ECOSAR software and the end product toxicity was also evaluated against E. coli and S. epidermis. The end product toxicity study also confirmed that the degraded product was less toxic compared to parent compound. Further, the genotoxicity study was done to understand the environmental impact using allium cepa and results confirms that there are no causes of cytotoxicity & genotoxicity by the prepared NCs. Therefore, the prepared NCs can be economical, efficient with excellent photocatalytic performance and environment friendly.

Sunlit expeditious visible light-mediated photo-fenton degradation of ciprofloxacin by exfoliation of NiCo2O4 and Zn0·3Fe2·7O4 over g-C3N4 matrix: A brief insight on degradation mechanism, degraded product toxicity, and genotoxic evaluation in Allium cepa.

Pharmaceutical pollutant in the environmental water bodies has become a major concern, which causes adverse effect to aquatic entities. This study provides an incisive insight on the photocatalytic degradation of ciprofloxacin (CIP) and the development of rationally engineered g-C3N4-NiCo2O4-Zn0.3Fe2·7O4 nanocomposite for boosted photocatalytic performance under visible light irradiation. The g-C3N4-NiCo2O4-Zn0.3Fe2·7O4 nanocomposite was synthesized via ultrasonication-assisted hydrothermal method. The characterization of the as-prepared material was evaluated by XPS, SEM, HR-TEM, PL, FT-IR, EIS, ESR, XRD, BET, and UV-Vis DRS techniques. Furthermore, the effect of catalytic dosage, drug dosage, and pH changes was explored, where g-C3N4-NiCo2O4-Zn0.3Fe2·7O4-10% unveiled excellent visible light photo-Fenton degradation of 92% for CIP at 140 min. The hydroxyl radicals (OH.) served as the predominant radical species on the photodegradation of CIP, which was confirmed by performing a radical scavenging test. Furthermore, the degradation efficiency was determined by six consecutive cycle tests, where the nanomaterial exhibited excellent stability with 98.5% reusable efficiency. The degradation of CIP was further scrutinized by GC-MS analysis, where the degraded intermediate products and the possible pathway were elucidated. The degraded product toxicity was determined by ECOSAR program, where the degraded products haven't exhibited any considerable toxic effects. In addition, the genotoxicity of the nanomaterial was determined by treating them with root tips of A. cepa, where it was found to be non-toxic. Here, the prepared g-C3N4-NiCo2O4-Zn0.3Fe2·7O4 nanocomposite (CNZ NCs) shows eco-friendly and excellent photo-Fenton activity for environmental applications.

Plasma-assisted in-situ preparation of L-cystine functionalized silver nanoparticle: An intelligent multicolor nano-sensing of cadmium and paracetamol from environmental sample.

L-cystine (L-cys) functionalized plasmonic silver nanomaterial (Ag NPs) was fabricated toward the selective and sensitive detection of paracetamol and cadmium. The prepared L-cys-Ag nanoparticles (NPs) were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction spectroscopy (XRD) and fourier transform infrared spectroscopy (FTIR) analyses. SEM imaging show that Ag NPs was decorated on the surface of L-cysteine 3D cubic nanosheet. L-cys-Ag NPs showed selective and sensitive detection towards paracetamol and cadmium. The interference study confirms that the presence of other metal ions didn't inhibit the detection of cadmium by L-cys-Ag NPs. The limit of detection of paracetamol and cadmium by L-cys-Ag NPs was calculated to be 1.2 and 2.82 nM respectively. In addition, the real sample detection of paracetamol on blood serum and urine, and cadmium on STP were performed and the recovery percentage was above 97%. Further, the real sample analysis was performed in tap and drinking water and the recovery percentage was more than 98%. The analytic logic gate on the multicolour detection of cadmium and paracetamol was performed for the semi-quantitative monitoring of paracetamol and cadmium by L-cys-Ag NPs. The developed L-cys-Ag NPs were found to be an effective tool for the monitoring of cadmium in environmental water bodies and paracetamol in blood and urine.

Self-assembling of 3D layered flower architecture of BiOI modified MgCr2O4 nanosphere for wider spectrum visible-light photocatalytic degradation of rhodamine B and malachite green: Mechanism, pathway, reactive sites and toxicity prediction.

In this study, 3D BiOI nanoparticle (BOI NPs) modified MgCr2O4 nanoparticle (MCO NPs) was fabricated by simple sonochemical and coprecipitation method for the enhanced photocatalytic activity. The morphological structure of the MgCr2O4-BiOI nanocomposite (MCO-BOI NCs) was characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV-visible diffuse reflectance spectroscopy (DRS), electron impedance spectroscopy (EIS) and photo luminescence (PL). The lower in the PL intensity and small arc in EIS for NCs shows the effective charge separation and lower in rate of recombination of charge carriers in NCs than the pure MCO and BOI NPs. The degradation efficiency of Rhodamine B (RhB) and malachite green (MG) by MCO-BOI NCs was found to be 99.5% and 98.2% receptivity. In addition, the photocatalytic degradation of RhB and MG was studied under various environmental parameters (different pH, varying the concentration of NCs and dyes) and response surface (RSM) plot was performed. The complete mineralization of RhB and MG by MCO-BOI NCs was determined by TOC. In addition, the photocatalytic degradation pathway was elucidated based on GC-MS results and Fukui function. In addition, the toxicity of intermediate formed during the degradation of RhB and MG was predicted by ECOSAR. The present work highlights the application of MCO-BOI NCs in environmental remediation for toxic pollutant removal.

Designing novel MgFe2O4 coupled V2O5 nanorod for synergetic photodegradation of tetracycline with enhanced visible-light energy harvesting: Photoluminescence, kinetics, intrinsic mechanism and bactericidal effect.

The present study focused on the enhancement of degradation of an important pharmaceutical pollutant, tetracycline with the help of nano photocatalyst under visible light irradiation. The study found that the synergetic effect of novel MgFe2O4-V2O5 enhanced the photocatalytic degradation of tetracycline. Here, the photocatalyst was synthesized by sonochemical technique. Scanning electron microscopy image indicates the coupling of MgFe2O4 nanocapsules on the surface of the V2O5 nanorod. The bandgap of MgFe2O4 (1.8 eV) and V2O5 (2.5 eV) was shifted to 2.32 eV in MgFe2O4-V2O5 to promote visible-light harvesting and it was depicted by the UV-visible DRS. XPS was used to identify the presence of chemical states with the existence of Mg 1s, Fe 2p, V 2p, and O 1s. The electrochemical impedance spectroscopy and photoluminescence spectra indicate the better separation of charge carriers owing to the formation of type II heterojunction formation. The tetracycline (25 mg/L) was degraded with MgFe2O4-V2O5 (150 mg/L) that exhibited 3.3 and 5 folds enhanced rates than its counterparts (MgFe2O4 and V2O5) owing to synergism. The possible intermediate formation and degradation pathway was determined based on GC/MS analysis. TOC analysis of end products indicated maximum mineralization of tetracycline. The MgFe2O4-V2O5 showed excellent recycling ability and reusability. The key photo-degradation of tetracycline was occurred by the generation of hydroxyl radicals. The MgFe2O4-V2O5 exhibited high antibacterial activity that ensures the dual functionality of the prepared nanocomposites (NCs). Therefore, the present study displays MgFe2O4 decorated V2O5 nanorod as an ideal candidate for environmental remediation.