Fabrication of MoS2 restrained magnetic chitosan polysaccharide composite for the photocatalytic degradation of organic dyes.

Chitosan (CS) polysaccharide is expected to exhibit greater ionic conductivity, which can be attributed to its increased amino group content when it is blended with different semiconducting materials. Herein, the work used this conducting ability of chitosan and prepared a heterogeneous MoS2-induced magnetic chitosan (MF@CS) composite via the co-precipitation method, which was used to scrutinize the catalytic performance with Methylene Blue (MB) and Malachite Green (MG) dyes by visible light irradiation. The saturation magnetization value of the MF@CS composite is found to be 7.8 emu/g, which is less when compared to that of pristine Fe3O4 (55.7 emu/g) particles. The bandgap of the MF@CS composite is âˆ¼ 2.17eV, which exceeds the bandgap (Eg) of bare MoS2 of 1.80 eV. The maximum color removal of 96.3 % and 93.4 % for MB and MG dyestuffs is recognized in the exposure of the visible spectrum, respectively. At a starting dye dosage of 30 mg/L, 0.1 g/L of MF@CS, a pH level of 8-11, and 70 min of contact with direct light. The photocatalyst provides extremely good durability for a maximum of five phases. Hence, the MF@CS matrix is a viable and appropriate substance for the efficient treatment of effluents containing dye molecules.

Construction of surface-rich MoS2 nanoflowers decorated on 2D layered MXene nanohybrid heterostructure for highly efficient and rapid degradation of oxytetracycline.

In this study, we successfully developed a hybrid architecture referred to as MoS2@MX, involving the integration of MoS2 layered onto MXene using a straightforward co-precipitation method. This innovative hybrid photocatalyst exhibited remarkable efficiency in removing oxytetracycline (OTC) molecules from aqueous solutions under visible-light irradiation. During the photocatalytic process, both MoS2 and MX played distinct yet complementary roles. MoS2 facilitated efficient electron transfer, while MX contributed to the generation of radicals. This unique collaboration resulted in a noteworthy 99 % oxidation efficiency for OTC degradation within a brief 60 min of visible light exposure in an aqueous environment. The radicals 1O2 and •OH were identified as the principal drivers behind OTC degradation, underscoring the vital role of the hybrid material. Mechanistically, the degradation of OTC involved several key steps, including C-H bond cleavage, de-carboxylation, C-N bond oxidation, and de-chlorination. Importantly, the MoS2@MX hybrid composite demonstrated remarkable stability, maintaining a noteworthy photocatalytic efficiency of 89 % for targeted OTC removal after undergoing five consecutive cycles. In conclusion, this study emphasizes the potential of the MoS2@MX hybrid material as an effective agent for degrading organic OTC compounds within aquatic environments. The hybrid's multifaceted roles and exceptional performance suggest promising applications in sustainable water treatment.

Tuning of interfacial HGO@CLS nanohybrid S-scheme heterojunction with improved carrier separation and photocatalytic activity towards RhB degradation.

Herein, we premeditated and invented the innovative hybrid photocatalyst 2D/2D CuLa2S4 on holey graphene oxide (HGO) (HGO@CLS) via the hydrothermal method. Electrochemical techniques demonstrate the action of HGO in the HGO@CLS photocatalyst as an effective medium for electron transfer. Combining bimetallic sulfides on porous HGO synergistically provides a higher negative conduction band edge (-0.141 V), greater photo response (10.8 mA/cm2), smaller charge transfer resistance (Rct = 1.79Ω), and lower photoluminescence (PL) spectral intensity. According to our research, the catalytic recitals are sped up when HGO is assimilated into CLS photocatalyst hetero-junction. Additionally, it lowers the reassimilation rate due to the combined mesh nanostructures and functionality of CLS and HGO. UV-Vis DRS, Mott-Schottky, PL, and Electrochemical impedance spectra (EIS) results manifested that the CuLa2S4/HGO makes the spatial separation competent and transference of charge carriers due to the photon irradiation and exhibits superior photocatalytic ability. Electron spin resonance (ESR) analysis confirmed that •OH and h+ were the predominant radical species responsible for Rhodamine B(RhB) degradation. Moreover, conceivable degradation ways of RhB were deduced according to the identified intermediates which are responsible for the degradation of recalcitrant products. To check the stability of the photocatalyst, revival tests were also carried out. Similarly, the oxidative byproducts created in the deprivation courses were looked at, and a thorough explanation for the mechanism of degradation was given.

Construction of ternary (1D/2D/3D) Fe2O3-supported micro pillared Cu-based MOF on chitosan with improved photocatalytic behavior on removal of paraquat.

A hetero-structured metal organic framework of Cu-BTC and Fe2O3 nano-photocatalyst were tethered over chitosan using the hydrothermal method and fabricated a hybrid porous nanocomposite (CS-Fe@Cu-BTC). X-ray diffractometer results exposed the existence of Fe2O3 peaks. Surface area measurements using BET showed a mesoporous structure and the formation of type IV adsorption isotherm for nanocomposite. XPS and SEM-EDAX confirmed the existence of Fe2O3 nanoparticles in the hybrid porous structure. The UV-vis diffuse reflectance absorption shape emphasized the role of Fe2O3 in enhancing the band gap of CS-Fe@Cu-BTC nanohybrid. The lower intensity photoluminescence spectra of the CS-Fe@Cu-BTC shows a competent charge partition and delayed the recombination of electron-hole pairs. The photo-mineralization efficiency of Cu-BTC and CS-Fe@Cu-BTC was evaluated in terms of electronic interactions using paraquat (PQT) as the probe molecule, which shows a mineralization of 91% at the pH range of ~ 5. The contribution of •OH in the degradation of PQT over CS-Fe@Cu-BTC nanocomposites revealed using the trapping test and the degradation mechanism follows the Langmuir-Hinshelwood model and pseudo-first-order kinetics. The durability of the CS-Fe@Cu-BTC nanocomposite was also established after four cycling processes.

Applications of chitin and chitosan based biomaterials for the adsorptive removal of textile dyes from water - A comprehensive review.

The presence of pollutants in the water bodies deteriorate the water quality and make it unfit for use. From an environmental perspective, it is essential to develop new technologies for the wastewater treatment and recycling of dye contaminated water. The surface modified chitin and chitosan biopolymeric composites based adsorbents, have an important role in the toxic organic dyes from removal wastewater. The surface modification of biopolymers with various organics and inorganics produces more active sites at the surface of the adsorbent, which enhances dye and adsorbent interaction more reliable. Herein, the work brought in the thought of the application of various chitin and chitosan composites in wastewater remediation and suggested the versatility in composites for the development of rapid, selective and effective removal processes for the detoxification of a variety of organic dyes. It further emphasizes the existing obstruction and impending prediction for the deprivation of dyes via adsorption techniques.

Photocatalytic performance of chitosan tethered magnetic Fe2O3-like (3D/2D) hybrid for the dynamic removal of anionic dyes: Degradation and mechanistic pathways.

Efficient photocatalysis methods with a production of less number of toxic intermediates are extremely advantageous for water decontamination. The degradation efficiency, specific surface area, stability and porosity will be improving by wrapping of Fe2O3 using appropriate biopolymers. In this work, Fe2O3 reinforced chitosan (Fe2O3@CS) nanocomposite was fabricated using co-precipitation method. The chitosan makes available its surface for the useful generation of the nanocomposite. These wrapping of Fe2O3 on chitosan provides synergistically improved properties that could be attributed to the elevated partition efficiency and faster transfer of the photo-generated charge carriers, which was substantiated by the experimental outcomes from photoluminescence and ESR spectroscopy. The results obtained from DRS analysis entail the reduction in band gap of Fe2O3@CS (2.52 eV) as compared with 3.52 eV of Fe2O3. The results indicated that 89.2% and 94.6% were the maximum degradations correspondingly for MO and OG. The trapping investigation emphasized the involvement of OH radicals in the degradation of dyes over Fe2O3@CS composites. The five cycles of regeneration experiment recommended the superior photostability of the fabricated Fe2O3@CS composite. This work proposed a practical arrangement and subsequent influence of an advanced photocatalyst for the useful remediation dyes from contaminated water without causing any secondary pollution.

Complex interior and surface modified alginate reinforced reduced graphene oxide-hydroxyapatite hybrids: Removal of toxic azo dyes from the aqueous solution.

In this study, alginate reinforced reduced graphene oxide@hydroxyapatite (rGO@HAP-Alg) hybrids have been fabricated via co-precipitation technique. The developed adsorbent was effectively utilized for the removal of Reactive Blue 4 (RB4), Indigo Carmine (IC) and Acid Blue 158 (AB158) azo dyes from aqueous solution, and found to have the adsorption efficiency of 45.56, 47.16 and 48.26 mg/g, respectively. The thermodynamic parameters demonstrated the endothermic and spontaneous nature of the adsorption process. The adsorption system was pH-dependent and showed maximum dye removal at pH 6-7, which was indicative of the electrostatic interactions, surface complexation and the hydrogen bonding mechanisms involved between the adsorbate and adsorbent during the adsorption process. Furthermore, the renewability studies demonstrated the reusability and stability of rGO@HAP-Alg hybrids up to five successive cycles. This study delivers a promising strategy for removing dye molecules and extends the potential application of rGO@HAP-Alg hybrids to treat practical dye contaminated water/wastewater.

Facile synthesis of Zr4+ incorporated chitosan/gelatin composite for the sequestration of Chromium(VI) and fluoride from water.

The development of industrialization and agricultural activities have carried various negative impacts to living organisms in recent decades and also, the frequent problem of inorganic pollution have been environmental anxiety to the community. Among these, Cr6+ and F- are priority poisonous pollutants from many industries. In this work, we present a low-cost synthesis procedure to obtain biocompatible zirconium incorporated chitosan-gelatin composite (CS-Zr-GEL) were fabricated and explored for the adsorptive removal of toxic Cr6+ and F- from water. The adsorption mechanism of toxic Cr6+ and F- was done by batch mode as a function of contact time, solution pH and co-existing ions. The obtained materials were extensively studied by several physico-chemical techniques to access their properties by X-ray diffraction (XRD), scanning electron microscopy with Energy Dispersive X-ray Spectroscopy (SEM-EDX), Fourier-transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC) analysis. Additionally, the fabricated adsorbent is highly dependent on solution pH. The kinetic and isotherm data were fitted using pseudo-second-order kinetic and Langmuir isotherm models. The maximum adsorption capacity for CS-Zr-GEL is 138.89 and 12.13 mg/g at 323K for Cr6+ and F- respectively. These findings demonstrate that the CS-Zr-GEL adsorbent represents a promising candidate that would have a practical influence on water/wastewater treatments.

Immobilization of MIL-88(Fe) anchored TiO2-chitosan(2D/2D) hybrid nanocomposite for the degradation of organophosphate pesticide: Characterization, mechanism and degradation intermediates.

In this study, we have rationally designed and grafted a bio-assisted 2D/2D TiO2/MIL-88(Fe) (TCS@MOF) heterojunction by growing granular TiO2 on the surface of MIL-88(Fe) nanosheet, as hybrid photocatalyst. The hierarchical TCS@MOF composite was prepared via the one-pot solvothermal process and employed for monocrotophos (MCP) degradation under visible light region, since its persistent nature on soil and water causes major threat to the environment. The TCS@MOF promotes a number of packed high-speed nano-tunnels in the (p-n) heterojunctions, which significantly enhance the migration of photo-induced electrons (e-) and holes (h+), respectively and thus limits the charge recombination of e-s. The optimized photocatalyst achieves significant catalytic activity of ~98.79% for the degradation of MCP within 30 min of irradiation. The prominent oxidative radicals namely •OH, •O2- etc., were involved in the oxidation of organic pesticide. Besides, TCS@MOF exhibits outstanding stability even after five repetitive cycles for the oxidation of MCP with a negligible decrease in photo-activity. The proposed mechanism and oxidative pathways of MCP were rationally deduced in detail subject to experimental results. The mechanism renders insight into the oxidation and consequent bond rupture of pollutant as well as into the formation of products such as H2O, CO2, etc. This report unveils a novel architecture of proficiently optimized TCS@MOF material structure for the perceptive oxidation of organic contaminants.

Boosted insights of novel accordion-like (2D/2D) hybrid photocatalyst for the removal of cationic dyes: Mechanistic and degradation pathways.

In the present work, a novel (2D/2D) accordion like CS@g‒C3N4/MX hybrid composite was prepared through one-pot hydro-thermal synthesis method and utilized as a catalyst for the degradation of organic persistent dyes such as methylene blue (MB) and rhodamine B (RhB). Because the removal of such organic compounds is a major dispute in environmental aspects. In this study, the bio-assisted g‒C3N4/MX nanosheets was utilized for the removal of organic dyes from aqueous solution under visible light irradiation, respectively. The CS@g-C3N4/MX photocatalyst showed high catalytic activity based on ~99% and ~98.5% degradation of MB and RhB within 60 and 40 min using visible light irradiation. This outcome could have resulted in greater catalytic enactment towards the degradation of other persistent pollutants with enhanced light absorption property and it can efficiently suppress photo-generated charge recombination, thus improving the interfacial charge transfer rate. The OH radical was being effective oxidative species involved in the CS@g-C3N4/MX system for the degradation of organic contaminants. Furthermore, CS@g-C3N4/MX showed excellent photo-stability over five consecutive cycles for the degradation of organic dyes with negligible loss of photocatalytic activity. Finally, the purposed catalytic mechanisms and degradation pathways of MB and RhB were systematically discussed in detail based on experimental results. Thus, the organics which oxidized into ring-opened compounds such as ethoxyethane, butadiene etc., to non-toxic products like H2O, CO2 and some mineral salts.

Synthesis and characterization of La(III) supported carboxymethylcellulose-clay composite for toxic dyes removal: Evaluation of adsorption kinetics, isotherms and thermodynamics.

The discharge of organic dyes into the aquatic environment is a serious problem owing to the persistence of possible health risks and ecological hazards of these pollutants. This paper reports a facile method for the preparation of composite material consisting of lanthanum incorporated carboxymethylcellulose-bentonite (LCB) composite and utilized for the removal of Indigo Carmine (IC), Acid Blue 158 (AB158) and Reactive Blue 4 (RB4) dyes from water by batch adsorption techniques. The optimal conditions for the dye adsorption were found to be pH = 3, initial dye concentration: 50 mg/L and adsorbent dosage of 100 mg. The adsorption efficiency of IC, AB158 and RB4 dye molecules were 80.41%, 83.54% and 86.91% respectively. The entire adsorption process was completed within 40 min. The adsorption data fits well with the pseudo-second-order kinetic model, demonstrating the physico-chemical adsorption of the dyes on LCB matrix. The Langmuir, Freundlich, and D-R isotherm models were used to describe saturation point. The fabricated adsorbent material was characterized using PXRD, FTIR, SEM-EDAX, TGA-DSC and surface area measurements. The thermodynamic studies revealed that the adsorption was spontaneous and endothermic in nature. The LCB composite showed remarkable adsorption-desorption efficiency for dye removal in water/wastewater treatment process; hence it can be considered as a competent and potential adsorbent for dye removal.

Chitosan modified zirconium/zinc oxide as a visible light driven photocatalyst for the efficient reduction of hexavalent chromium.

Metal-sensitized biopolymeric hybrid materials can be strategically utilized in photo catalysis due to the behavior of their absorption band lying in the solar radiation spectrum. Herein, chitosan supported zirconium(Zr)/zinc oxide (ZnO)) in the preparation of photo catalyst (Zr-ZnO@CS) for photocatalytic reduction of hexavalent chromium(Cr6+). Moreover, photocatalytic testing factors like exposure time of light, pH, initial Cr6+ concentration, and influence of co-anions on the removal of Cr6+ by Zr-ZnO@CS were also examined. Langmuir-Hinshelwood kinetic model suggested the surface reaction was the rate-controlling step. The removal mechanism of Zr/ZnO@CS was because of enhanced properties like positive positioning of the band gap, boosted charge excitation, and higher dynamic sites. Field trial results showed that Zr-ZnO@CS hybrid photocatalyst demonstrates the potential application for the reduction of Cr6+ ions.

Adsorptive performance of lanthanum encapsulated biopolymer chitosan-kaolin clay hybrid composite for the recovery of nitrate and phosphate from water.

Nitrate and phosphate are primary pollutants of water/wastewaters for eutrophication and methemoglobinemia diseases, harshly threatening the security of aquatic environments and human health as well as all living beings. The present work investigates the adsorption performance and mechanism of lanthanum encapsulated chitosan-kaolin clay (LCK) hybrid composite was prepared and utilized for the remediation of nitrate and phosphate from water. The fabricated LCK hybrid composite was characterized using XRD, SEM, BET, EDAX, TGA-DTA and FTIR analysis. The removal of nitrate and phosphate onto the LCK composite defined by pseudo-second-order kinetic model whereas the isotherms are described by Freundlich adsorption isotherm model and thermodynamic experiments showed spontaneous and exothermic nature of the adsorption process. Results also demonstrated that the LCK hybrid composite exhibited extremely high nitrate and phosphate adsorption capacity and stability which followed the mechanisms by ion exchange, complexation and electrostatic interactions. Adsorption-desorption experiments revealed that the LCK hybrid composite could be potentially reused with maintaining high adsorption efficiency. This study highlights the novel low-cost, eco-friendly and promising adsorbent for efficient denitrification and dephosphorization from water/ wastewater.

Enhanced photocatalytic response of ZnO embedded chitosan/ß-cyclodextrin towards the detoxification of Cr(VI) under visible light.

The present work focused on the assessment of heterogenous photocatalytic efficacy of ZnO@CS-ß-CD towards the degradation of hexavalent chromium under visible light illumination. The prepared ZnO@CS-ß-CD was extensively characterized using XRD, FTIR, SEM, EDX with mapping, TGA, DSC and UV/vis DRS techniques and the photoreduction of Cr(VI) to Cr(III) was confirmed by X-ray photoelectron spectroscopy. The DRS results revealed that the band gap of ZnO@CS-ß-CD was narrowed than ZnO from 3.23 to 2.01 eV. The photocatalyst hold excellent reusability up to seven cycles and the field trail results demonstrated for the practical application for the treatment of wastewater.

Removal of chlorpyrifos, an insecticide using metal free heterogeneous graphitic carbon nitride (g-C3N4) incorporated chitosan as catalyst: Photocatalytic and adsorption studies.

The present study investigates the photocatalytic degradation of an organic pesticide using a metal free heterogeneous graphitic carbon nitride (g-C3N4) incorporated into chitosan as catalyst. Chlorpyrifos (O, O-diethylO-3,5,6-trichloro-2-pyridyl phosphorothioate (CPFS)), an insecticide includes in a class of Organophosphate pesticides with a chemical formula (C9H11Cl3NO3PS). It is widely used in agricultural lands to control pests in cotton, fruit and vegetables. The acute toxicity of chlorpyrifos is still dangerous to all aquatic living organisms. The CS/g-C3N4 materials have been characterized using UV-vis spectrophotometer (UV-vis), Fourier transform infrared spectroscopy (FTIR), Scanning electron microscope (SEM), Energy Dispersive X-ray Analysis (EDX), Thermal analysis (TGA-DSC), Chemical oxygen demand (COD), X-ray diffraction (XRD), Diffuse reflectance spectra (DRS) and Electron spin resonance (ESR). The degradation of pesticide using CS/g-C3N4 showed good efficiency of about 85%. The results suggest that CS/g-C3N4 composite is a good alternative for the treatment of chlorpyrifos in aqueous solution. We have proposed a novel photocatalyst by metal free heterogeneous graphitic carbon using melamine and its recombination effects were minimized by chitosan which act as an electron carrier. The enhanced photocatalytic performance could be attributed to an efficient separation of electron-hole pairs through a Z-scheme mechanism, in which chitosan acted as charge separation carriers.

Performance of chitosan engraved iron and lanthanum mixed oxyhydroxide for the detoxification of hexavalent chromium.

The iron - lanthanum mixed oxyhydroxide (FLMOH) and chitosan engraved iron - lanthanum mixed oxyhydroxide materials (CSFLMOH) were prepared successfully and utilized for the hexavalent chromium adsorption studies. The physicochemical properties of pristine and Cr(VI) treated adsorbents were characterized using XRD, FTIR, SEM with EDX, TGA and DSC analysis. The efficacy of the CSFLMOH was compared with FLMOH towards the uptake of Cr(VI) ions and was explored using batch technique under various influencing parameters viz., time, dose, pH, initial concentration and co-existing anions. Langmuir, Freundlich and Dubinin - Radushkevich isotherms were used to analyze the adsorption behavior at 303, 313 and 323 K. The rate of the reaction was calculated using reaction based and diffusion-based models. Recycle and reuse studies were demonstrated using 0.05 M NaOH as the desorbing medium.