Enhanced visible light driven photodegradation of rifampicin and Cr(VI) reduction activity of ultra-thin ZnO nanosheets/CuCo2S4QDs: A mechanistic insights, degradation pathway and toxicity assessment.

In this study, we focused on fabrication of porous ultra-thin ZnO nanosheet (PUNs)/CuCo2S4 quantum dots (CCS QDs) for visible light-driven photodegradation of rifampicin (RIF) and Cr(VI) reduction. The morphology, structural, optical and textural properties of fabricated photocatalyst were critically analyzed with different analytical and spectroscopic techniques. An exceptionally high RIF degradation (99.97%) and maximum hexavalent Cr(VI) reduction (96.17%) under visible light was achieved at 10 wt% CCS QDs loaded ZnO, which is 213% and 517% greater than bare ZnO PUNs. This enhancement attributed to the improved visible light absorption, interfacial synergistic effect, and high surface-rich active sites. Extremely high generation of ●OH attributed to the spin-orbit coupling in ZnO PUNs@CCS QDs and the existence of oxygen vacancies. Besides, the ZnOPUNs@CCS QDs, forming Z-scheme heterojunctions, enhanced the separation of photogenerated charge carriers. We investigated the influencing factors such as pH, inorganic ions, catalyst dosage and drug dosage on the degradation process. More impressively, a stable performance of ZnO PUNs@CCS QDs obtained even after six consecutive degradation (85.9%) and Cr(VI) reduction (67.7%) cycles. Furthermore, the toxicity of intermediates produced during the photodegradation process were assessed using ECOSAR program. This work provides a new strategy for ZnO-based photocatalysis as a promising candidate for the treatment of various contaminants present in water bodies.

Construction of Ag/CdZnS QDs nanocomposite for enhanced visible light photoinactivation of Staphylococcus aureus.

With increasing use of antibiotics, the development of antibiotic-resistant pathogens poses a serious threat to human health and the environment. Photocatalytic inactivation of these harmful pathogens is one of the novel and non-antibiotic treatments. The study fabricated Ag NPs decorated CdZnS QDs via a facile and biological co-precipitation method using L. camara plant extract as a green alternative to treat the toxic chemicals. The fabricated Ag/CdZnS QDs (NCs) were prepared for the efficient treatment of antibiotic-resistant pathogens as they raise a major global concern. The fabricated NCs were characterized with various characterization techniques to verify its physicochemical properties. The fabricated NCs have shown excellent photo-sterilization performance of 97 % against S. aureus. The excellent activity was attributed to the decoration of Ag NPs on CdZnS QDs as it helped in shortening band gap, improved visible light absorption ability, increased active sites, and boosted photogenerated electron/hole pairs stability. Radical trapping experiment and ESR analysis indicated the involvement of •OH and h+ in the photoinactivation of bacteria. The photo sterilization reaction of NCs was carried out under different environmental conditions, including light and dark conditions and different pH conditions. The experiment was carried out in sewage-treated water in order to test the real-time application, and the fabricated NCs achieved excellent 95.9 % photo-inactivation of S. aureus cells in sewage treated water and the Chemical Oxygen Demand (COD) of the system was increased after photo inactivation treatment. The fabricated NCs have also shown excellent reusable efficiency of 95% after six runs and the photostability and anti-corrosive nature of NCs were confirmed. The study provides an insight for the employment of photocatalysis for the sterilization of pathogens in real time aquatic environment across the globe.

Interstitial decoration of Ag linking 3D Cu2O octahedron and 2D CaWO4 for augmented visible light active photocatalytic degradation of rifampicin and genotoxicity studies.

A morphological oriented highly active Cu2O-Ag-CaWO4 (CAC) nano-heterojunction was fabricated for the visible light driven degradation of rifampicin (RFP). Octahedron shaped Cu2O being a base material, where the Tagetes shaped CaWO4 and Ag were embedded on it. The shape-controlled morphology of Cu2O and CaWO4 as well as Ag decoration influence high degree of adsorption of RFP and interfacial charge transfer between the nano-heterojunction. Further, the larger specific surface area (129.531 m2/g) and narrow band gap energy (2.57 eV) of CAC nano-heterojunction than the controls support the statement. Positively, CAC nano-heterojunction following Z-scheme-type charge transport mechanism attained 96% of RFP degradation within 100 min. O2•- and •OH are the primarily involved reactive oxidation species (ROS) during the photocatalytic reactions, determined by scavenger study and ESR analysis. The stability and reusability of the CAC nano-heterojunction was assessed through performing cyclic experiment of RFP degradation and it holds 96.8% of degradation even after 6th cycle. The stability of CAC nano-heterojunction after photodegradation was further confirmed based on crystalline pattern (XRD analysis) and compositional states (XPS analysis). Intermediates formed during RFP degradation and its toxicity was discovered by using GC-MS/MS and ECOSAR analysis respectively. The end-product toxicity against bacterial system and genotoxicity of CAC nano-heterojunction against Allium cepa were evaluated and the results were seemed to have no negative causes for the aquatic lives.

Construction of p-n-p nano heterojunction through coupling La2O3, (BiO)2CO3 and Ag3PO4 for effective photocatalytic degradation of doxycycline: Insights into mechanism, pathway and intermediate toxicity evaluation.

The present work is centred around the development of La2O3/(BiO)2CO3/Ag3PO4 (LBA), a p-n-p nano-heterojunction to photodegrade doxycycline under visible light irradiation. Here, ultrasonication assisted co-precipitation method was employed to synthesize the photocatalyst. The photocatalyst was characterized using different analysis such as SEM, TEM, elemental mapping, XRD, XPS, FTIR, Raman, BET, DRS, PL and EIS which confirmed the successful fabrication of LBA and their excellent ability to refrain the e-/h+ recombination owing to the construction of the heterojunction. LBA was found to degrade DOX by 91.75 % with the high mineralization of 87.23%. The impact of the reaction parameters influencing the photodegradation process including the concentration of the NCs and DOX, pH and the influence of the commonly present anions were studied. The stability and reusability of the LBA was assessed through subjecting it to four cycles of photodegradation of DOX. In addition, the recovered LBA was characterized through XPS and XRD analysis to confirm the particles stability and reusability. The active participation of the photogenerated charges and the reactive oxygen species were identified through the scavenging assay and ESR analysis. Further, GC-MS/MS analysis was performed to put forward a plausible photodegradation pathway. The toxicity of the end products as well as the intermediates was predicted through ECOSAR software.

Unravelling the enhanced rifampicin photocatalytic degradation over green-synthesized SrO2@SnIn4S8 p-n heterojunction: Pathway, toxicity evaluation and mechanistic insights.

In recent years, the discharge of pharmaceutical drugs into aquatic ecosystems has become a growing concern, posing a significant threat to aquatic life. In response to this environmental challenge, advanced oxidation processes have gained prominence in wastewater treatment due to their efficacy in eliminating pharmaceutical pollutants and their potential for reusability. In this study, we have fabricated SnIn4S8 coupled SrO2 nano-heterojunction (NH) using a greener co-precipitation approach using leaf extract derived from Acaphyla wilkesiana. The resulting NH exhibited exceptional photocatalytic activity against rifampicin (RIF), achieving a remarkable 97.4% degradation under visible light, surpassing the performance of its individual components. The morphological characteristics of the NH were thoroughly analyzed through SEM, TEM, XRD, and XPS techniques, while EIS, DRS, and BET techniques provided valuable insights into its photocatalytic and optical properties. Furthermore, radical scavenging assays and ESR analysis identified hydroxyl radicals (•OH) and superoxide radicals (O2•-) were the species contributing to the visible light-driven photocatalytic degradation. The study also elucidated the potential degradation pathways and intermediates of RIF through GC-MS analysis. Additionally, the toxicity of the produced intermediates was assessed using the ECOSAR model. The findings have significant implications for the treatment of pharmaceutical pollutants and underscore the importance of eco-friendly synthesis methods in addressing environmental challenges.

Congregating Ag into γ-Bi2O3 coupled with CoFe2O4 for enhanced visible light photocatalytic degradation of ciprofloxacin, Cr(VI) reduction and genotoxicity studies.

The work attempts to construct a highly effective γ-Bi2O3/CoFe2O4/Ag visible active photocatalyst for the enhanced degradation of ciprofloxacin (CIP) and Cr(VI) reduction. γ-Bi2O3/CoFe2O4/Ag photocatalyst was prepared by simple solid phase and co-precipitation methods. The nanosphere shaped CoFe2O4 photocatalyst are embedded on top of γ-Bi2O3 nanotriangle. The addition of Ag into γ-Bi2O3/CoFe2O4 heterojunction primitively facilitates the photocatalytic activity in higher rate. The quantitative analysis of photocatalyst possesses to have lower e-/h+ recombination rate compared to its counterparts. The prepared γ-Bi2O3/CoFe2O4/Ag photocatalyst showed 96.6% degradation of CIP in 220 min and 99.2% reduction of Cr(VI) in 120 min. Additionally, γ-Bi2O3/CoFe2O4/Ag showed outstanding recyclability and long-term stability with a degradation efficiency of 96.5% even after six cycles. The intermediate products formed were identified and the degradation pathway was elucidated by gas chromatography-mass spectrometry analysis. Total organic carbon measurement was carried over to assess the efficiency of complete degradation and the removal percentage was found to be 98%. The end product toxicity study towards bacteria was proven to have less toxicity level when compared to parent compound. Lastly, the genotoxicity of γ-Bi2O3/CoFe2O4/Ag photocatalyst was tested in Allium cepa and the results confirmed to have no cause of toxicity impacts. Overall, the work not only tends to provide a highly visible active γ-Bi2O3/CoFe2O4/Ag photocatalyst, but also attributes to have no further negative imprints in the environment.

Synergistic visible light assisted photocatalytic degradation of p-chlorophenol and rifampicin from aqueous solution using a novel g-C3N4 quantum dots incorporated α-MoO3 nanohybrid - Mechanism, pathway and toxicity studies.

In this work, a simple g-C3N4 quantum dots enriched MoO3 nanohybrid was formulated for the synergistic photocatalytic degradation of an industrially active organic pollutant, p-chlorophenol (PCP) and a widely prescribed antibiotic, rifampicin (RIF). The nanohybrid was synthesised via a facile ultrasonic assisted hydrothermal method and characterized using various characterization analysis. The efficient Z-scheme charge transfer of the nanohybrid resulted in the elimination of 98% PCP and 89% RIF under visible light with a rate constant of 0.012 and 0.006 min-1 respectively. The photocatalysis was attributed to the formation of both hydroxyl (OH•) and superoxide (O2•-) radicals in the resulting nanohybrid. The intermediates formed in the course of reaction were estimated through gas chromatography-mass spectroscopy/mass spectroscopy (GC-MS/MS) analysis and a suitable degradation pathway was constructed. The structural stability and reusability of the nanohybrid was affirmed through X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) analysis to outweigh the industrial potential of the catalyst, with 85% PCP and 80% RIF removal efficiency after six cycles of degradation. In addition, the mineralization of the pollutants was confirmed by total organic carbon analysis. Further, the toxicity of the drug and the formed intermediates was determined using ecological structure activity relationships (ECOSAR) software. On the whole, this work provides an excellent insight for the development of environment-friendly materials in a large scale for the degradation of water-based pollutants.

Self-propelled nanojets an interfacial Schottky junctions modulated oxygen vacancies enriched for enhanced photo-Fenton degradation of organic contaminant: Improving H2O2 generation, Fe3+/Fe2+ cycle and enhancing plant metabolism.

The study reports an innovative approach on sunlit driven heterostructure photocatalytic generation of H2O2 and removal of cefixime. In the present work, we have fabricated Mn/Mg doped CoFe2O4 modified CaCr2O4 decorated by Ag3PO4 quantum dots (Ag3PO4 QDs), a p-n-p nano heterojunction. The study promotes the photocatalytic production of H2O2 and self-Fenton photocatalytic degradation of cefixime. Egg white-assisted synthesis of Mn-doped CoFe2O4 causes the lattice oxygen defect, which enhances the photocatalytic activity. Lattice oxygen defect enable the adsorption of O2, which enable the conversion of •O2 in the valence band of CoFe2O4 for the endogenous production of H2O2. The higher in the surface area enhance the photocatalytic activity under visible light irradiation. Mn-CoFe2O4-CaCr2O4-Ag3PO4 QDs enables the complete photocatalytic degradation of cefixime (99.9%) and the complete removal was determined by total organic carbon (TOC) removal and it was around 99.4%. Meanwhile the photocatalytic degradation pathway of cefixime was determined by LC-MS/MS. Reusability of the nano heterojunction was determined by six cycle test, and the reusability of the nano heterojunction was 99.8%. Further, the toxicity of the nanomaterial was studied in maize plant and the results shows that the nanoheterojunction enhances the maize growth. The study systematically reveals the robust activity of nano heterojunction for sustainable water treatment.

Sunlight promoted self-fenton photodegradation and pathway of doxycycline: Interactive effects of nanomaterial on bean plant and its genotoxicity against Allium cepa.

Photocatalytic induction of electron/hole recombination, surface property and light response ability effectively enhance the photocatalytic activity of nanomaterial. In this work, the effective charge carrier separating Sn/Mn-ZnFe2O4-CdFe2O4-Ag3PO4 Quantum dots (M/SZFO-CFO-AP QDs) was fabricated for photocatalytic degradation of doxycycline (doxy) antibiotic. The result showed enhanced photocatalytic activity of doxy and the degradation efficiency of doxy was about 98.8% in short span of time. The calculated WH plot and urbach energy of prepared photocatalyst exhibited evidence for the prevalence of point defects and its contribution to efficient charge separation and transferability. The total organic carbon (TOC) removal was found to be 98.9%, which depicts the complete mineralization of doxy. The synergetic charge transfer of n-p-n heterojunction enables the effective removal of doxy under visible light irradiation. Further, the genotoxicity study was determined by interacting the SZFO-CFO-AP QDs with Allium Cepa. The results depict that SZFO-CFO-AP QDs show lower toxicity level and there were no trace of defective mitotic phases and micro nuclei. Further, the progression and development of bean plant was determined after treating with prepared nanomaterials and the result showed the enhanced growth in SZFO-CFO-AP QDs treated bean plant compared to the counterparts. Therefore, the prepared SZFO-CFO-AP QDs was can be used as an environmental friendly photocatalyst for effective treatment of antibiotic present in the water bodies.

Eco-friendly cubic-ZnS coupled Cu7S4 spines on chitosan matrix: Unravelling defect-engineered nanoplatform for the photodegradation of p-chlorophenol.

Novel ZnS-Cu7S4 nanohybrid supported on chitosan matrix, as an ideal photocatalyst, was fabricated by the sonochemical method wherein high-resolution transmission electron microscopy (HRTEM) and X-ray powder diffraction (XRD) analysis confirmed the co-existence of both ZnS and Cu7S4; presence of vacancy sites in ZnS was verified by electron paramagnetic resonance (EPR) analysis and their introduction could promote two-photon excitation facilitated visible light response and charge transport/separation. The type II interface is formed in the ZnS-Cu7S4/Chitosan heterojunction owing to interstitial states that promote charge separation. The ZnS-Cu7S4/Chitosan was used for the photodegradation of a pharmaceutical pollutant, p-chlorophenol (PCP); over 98.8% of PCP photodegradation was achieved under visible-light irradiation where the ensued ·O2- and ·OH serve a key role in the photodegradation of PCP. In vitro cytotoxicity studies substantiated that the ZnS-Cu7S4/Chitosan is nontoxic to the ecosystem and human beings and endowed with promising photodegradation properties and accessibility via an environmentally friendly design, bodes well for its potential remediation applications.

Enhanced photodegradation of rifampicin and co-trimoxazole by ZnO/ZnMn2O4/ZnS-PVA and its genotoxicity studies on Allium cepa.

Oxygen vacancies and its associated defect states have a great influence on the electronic and structural aspects of semiconductor photocatalysts, yet there is paucity of investigations about the influence of the defect states on their photocatalytic properties. Herein, this study reports the hierarchical fabrication of oxygen vacancy enriched ZnO/ZnMn2O4/ZnS-PVA nanocomposite (NCs) for the enhanced photodegradation of rifampicin and co-trimoxazole. The formation of lattice expansion induced oxygen vacancies and its associated Urbach tail energy, and n-p-n heterojunction-based S-scheme charge transfer path synergistically contributed to the boosted photocatalytic performance of the as prepared NCs. The photocatalytic performance of the nanomaterial towards rifampicin and co-trimoxazole has been determined to be 80% and 90% under visible light irradiation, respectively. Furthermore, various operating parameters including the concentration of NCs and drug, pH and interference of various ions have been evaluated. The degraded product intermediates have been elucidated by GC-MS analysis. The toxicity of the as-prepared nanomaterials has been evaluated by treating the samples with root tips of Allium cepa, where the NCs was found to be non-toxic. The study provides a new-fangled insight on the preparation and fabrication of non-toxic and defect rich nanomaterials which may help stimulate this area of research.

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.

Photodegradation of 5-flurouracil, carvedilol, para-chlorophenol and methimazole with 3D MnWO4 nanoflower modified Ag2WO4 nanorods: A non-genotoxic nanomaterial for water treatment.

The present study focused on the photocatalytic degradation of 5-Flurouracil (FU), carvedilol (Car), para-chlorophenol (PCP) and methimazole (Met) under visible light irradiation by MnWO4/Ag2WO4 (MWO/AWO) nanohybrid. Here, MWO/AWO nanohybrid was characterized by XRD, TEM, EDS, XPS, ESR, EIS, BET and DRS. The band gap energy of the MWO/AWO nanohybrid was found to be 2.75 eV, which enables effective photocatalytic activity of nanohybrid under visible light. The photocatalytic degradation of various PhACs such as Fu, Car, PCP and Met was found to be 98.8, 100, 98 and 98.1% respectively. The degradation efficiency of the MWO/AWO nanohybrid on various PhACs was higher than the pure MWO and AWO nanoparticle. The effective formation of OH• and •O2 by MWO/AWO nanohybrid played an important role in degradation of PhACs and it was determined by radical scavenging experiment. Further, the intermediates formed during the photocatalytic process were analyzed by GC-MS/MS to elucidate the photodegradation pathway and the results reveal the complete mineralization of the PhACs. The toxicity of the degraded product was performed against on Bacillus subtilis and Escherichia coli where it shows that the nanohybrid possesses high relative growth inhibition than AWO and MWO nanoparticles. In addition, the genotoxicity of the nanohybrid against Allium cepa was performed and it exhibited lower toxicity. The synthesized nanohybrid proves to be an excellent photocatalyst with good stability, reusability, eco-friendly, and cost-effective material for implementation in practical applications.

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.