All-solid-state Z-scheme ZnFe-LDH/rGO/g-C3N5 heterojunction for enhanced sonophotocatalytic degradation of ciprofloxacin: Performance and mechanistic insights.

The fabrication of all-solid-state Z-scheme sonophotocatalysts is vital for improving the transfer rate of photogenerated electrons to remove antibiotics present in wastewater. Herein, a novel indirect Z-scheme ZnFe-layered double hydroxide (LDH)/reduced graphene oxide (rGO)/graphitic carbon nitride (g-C3N5) heterojunction was synthesized using a simple strategy. The ZnFe-LDH/rGO/g-C3N5 (ZF@rGCN) ternary composites were systematically characterized using different techniques. Results revealed that the 15%ZF@rGCN catalyst achieved a ciprofloxacin (CIP) degradation efficiency of 95% via the synergistic effect of sonocatalysis and photocatalysis. The improved sonophotocatalytic performance of the ZF@rGCN heterojunction was attributed to an increase in the number of active sites, a Z-scheme charge-transfer channel in ZF@rGCN, and an extended visible light response range. The introduction of rGO further enhanced the charge-transfer rate and preserved the reductive and oxidative sites of the ZF@rGCN system, thereby affording additional reactive species to participate in CIP removal. In addition, owing to its unique properties, rGO possibly increased the absorption of incident light and served as an electronic bridge in the as-formed ZF@rGCN catalyst. Finally, the possible CIP degradation pathways and the sonophotocatalytic Z-scheme charge-migration route of ZF@rGCN were proposed. This study presents a new approach for fabricating highly efficient Z-scheme sonophotocatalysts for environmental remediation.

Photodegradation of rhodamine-B in aqueous environment using visible-active gC3N4@CS-MoS2 nanocomposite.

Rapid industrial expansion leads to environmental pollution especially in an aqueous environment. Photocatalytic degradation is one of the most efficient and environmentally friendly techniques used to treat industrial pollution due to its complete degradation capability of a variety of water contaminants to their non-toxic state. Graphitic carbon nitride (gC3N4) and molybdenum disulfide (MoS2) provide efficient dye degradation, but MoS2 has few disadvantages. Hence, chitosan (CS) supported gC3N4-MoS2 hybrid nanocomposite was developed in this study to reduce these issues by accelerating the degradation of dye molecules such as rhodamine-B under visible light. The prepared gC3N4@CS-MoS2 hybrid nanocomposite was thoroughly characterized using various analytical tools including FTIR, XRD, SEM, EDX, XPS, UV-Visible, and PL spectra. Several influencing parameters such as irradiation time, initial pH, dosage, and initial dye concentration were optimized by batch mode. The photodegradation of rhodamine-B could be induced by the heterogeneous gC3N4@CS-MoS2-water hybrid nanocomposite. The narrow band gap of gC3N4@CS-MoS2 (1.80 eV) makes it suitable for effective degradation of rhodamine-B due to more active in the visible region and attained its highest degradation efficiency of 99% after 40 min at pH 8 with minimum dosage of 60 mg. The possible degradation mechanism was tentatively proposed for rhodamine-B dye molecules from aqueous environment. The present work shows a novel photocatalyst for the purification and detoxification of dye molecules as well as other water contaminants found in polluted wastewater.

Synthesis of magnetic chitosan biopolymeric spheres and their adsorption performances for PFOA and PFOS from aqueous environment.

Due to numerous applications and excellent environmental stability, long-chain perfluorinated chemicals (PFCs) are ubiquitous in water across the world and adversely affect the living organisms. Thus, this study focused on the mitigation of the most frequently used long-chain PFCs namely perfluorooctanoate (PFOA) and perfluorooctane sulfonate (PFOS) from water using reduced graphene oxide modified zinc ferrite immobilized chitosan beads (rGO-ZF@CB) as an adsorbent. The results from the adsorption isotherm and kinetic studies revealed that the adsorption data fitted well to the Langmuir and the pseudo-second-order models. According to the Langmuir isotherm, the rGO-ZF@CB possessed the maximum adsorption capacity of 16.07 mg/g for PFOA and 21.64 mg/g for PFOS. Both the electrostatic attractions and hydrophobic interactions have driven the removal of PFOA and PFOS by prepared rGO-ZF@CB. Eventually, the rGO-ZF@CB could be considered as an efficient adsorbent for the effective removal of PFOA and PFOS molecules from the aqueous environment.

Magnetic kaolinite immobilized chitosan beads for the removal of Pb(II) and Cd(II) ions from an aqueous environment.

In recent decades, magnetic bead material has attracted considerable attention in water and wastewater purification. In this study, the potential of magnetic kaolinite immobilized in chitosan beads (MKa@CB) to remove Pb(II) and Cd(II) ions from an aqueous environment has been successfully investigated. The addition of magnetic kaolinite generates more active sites, whereas that of chitosan enhances the stability of synthesized bead materials, which enable them to effectively interact with the targeted contaminants. Various factors including agitation time, solution pH, and competitive ions were examined to optimize the removal efficiency of the MKa@CB. The adsorption kinetics and isotherm studies indicated that the adsorption fitted well to the pseudo-second-order kinetic model as well as to the Langmuir isotherm. The prepared adsorbent could be reused up to four cycles without any significant adsorption capacity loss. Thus, the synthesized MKa@4%CB can be a promising adsorbent in effectively removing Pb(II) and Cd(II) from water.

Magnesium ferrite-reinforced polypyrrole hybrids as an effective adsorbent for the removal of toxic ions from aqueous solutions: Preparation, characterization, and adsorption experiments.

Contaminated waters with high contents of toxic anions are detrimental to the human health and wildlife. Thus, the quality of drinking water should be carefully monitored. Adsorption technique has been determined to be a reasonable strategy out of several methods used to remove toxic anions from water. Novel MgFe2O4-reinforced polypyrrole (Ppy@x%MgFe2O4) (x = 1%, 2%, and 5% of MgFe2O4) hybrids were synthesized from a pyrrole monomer and MgFe2O4 using a simple chemical oxidation method. The fabricated hybrids were studied for their capability to remove PO43-, NO3-, and Cr(VI) from aqueous solutions. The results showed that PO43-, NO3-, and Cr(VI) removal was highly pH-dependent. The adsorption isotherms of hybrids were fitted well by the Langmuir model, with the maximum adsorption efficiency of 116.90, 76.14, and 138.60 mg/g for PO43-, NO3-, and Cr(VI), respectively. In addition, the above-mentioned toxic anions could be efficiently desorbed from spent Ppy@x%MgFe2O4 using a 0.1 M NaOH solution, and the hybrids exhibited good regenerability. The prepared materials are promising candidates for PO43-, NO3-, and Cr(VI) removal and exhibit high adsorption efficiency, rapid adsorption-desorption behavior, and appropriate recovery from the aqueous medium under external magnetic field.

Effective adsorption of oil droplets from oil-in-water emulsion using metal ions encapsulated biopolymers: Role of metal ions and their mechanism in oil removal.

Herein, synthesized and compared the three different kinds of hybrid bio-polymeric composites viz., lanthanum embedded chitosan/gelatin (La@CS-GEL), zirconium embedded chitosan/gelatin (Zr@CS-GEL) and cerium embedded chitosan/gelatin (Ce@CS-GEL) in terms of their oil uptake efficiency. The adsorption efficiency was studied under various optimized parameters like contact time, pH, dose, initial oil concentration and temperature. The oil adsorption capacity was found to be 91, 82 and 45% for La@CS-GEL, Zr@CS-GEL and Ce@CS-GEL composites respectively. The metals were used as a bridging material to connect both CS and GEL using the hydrophilic groups to enhance the oil recovery by hydrophobic interaction. Also, the introduction of metal ions on the surface of biopolymers would modify the oil/water properties which in turn, decrease the interfacial tension between oil and water phases. The mechanism of oil uptake was explained using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscope (SEM), energy dispersive X-ray (EDAX) and heat of combustion. The experimental data confirmed Langmuir isotherm as the best fit for oil adsorption process. Thermodynamic parameters such as standard free energy (ΔG°), standard enthalpy (ΔH°) and standard entropy (ΔS°) indicated that the oil adsorption was spontaneous and endothermic. The oil adsorption mechanism was established based on isotherm and thermodynamic models.

Synthesis and characterization of chitosan/Mg-Al layered double hydroxide composite for the removal of oil particles from oil-in-water emulsion.

The recovery of oil from oil-in-water emulsion has been investigated using chitosan/magnesium-aluminium layered double hydroxide hybrid composite (CS-LDHCs) by a single co-precipitation method. Resulting better adsorption efficiency of CS-LDHCs could be observed, indicating the synthesized material was effective to adsorb oil particles from oil-in-water emulsion at acidic pH (pH 3.0) than as-prepared LDH and raw chitosan. The enhancement of adsorption properties by CS-LDHCs material were attributed to the high content of LDH in chitosan, which makes the material more effective towards immobilization of oily particles. Batch experiment study has been elucidated by varying different physicochemical parameters such as time, pH, dose, initial oil concentration and temperature. The as-synthesized CS-LDHCs was characterized by various spectro analytical techniques viz., FTIR, SEM with EDAX, XRD, TGA and DSC analysis. To find out the best fit for the sorption process, the obtained adsorption equilibrium data was explained with Freundlich, Langmuir, Dubinin-Radushkevich and Tempkin isotherm models. The mechanism of adsorption process was demonstrated by calculating ΔG°, ΔH° and ΔS° values from thermodynamic parameters in order to understand the nature of sorption process. The schematic representation of oil removal using CS-LDHCs was explored in detail. This work provides an apparent proposal for the growth of oil removal technology.

Defluoridation of water by Tea-bag model using La(3+) modified synthetic resin@chitosan biocomposite.

The aim of this work is to gain a better understanding of the formation of lanthanum complex onto iminodiacetic acid and chitosan (CS@La-IDAMP) composite for effective removal of fluoride from aqueous solution using a tea-bag model for the first time. The surface textural and chemical properties of the synthesized composites were characterized by FTIR, SEM with EDAX and mapping images. The experimental data revealed that the fluoride adsorption was rapid, maximum fluoride removal could be removed within 12min contact time at neutral pH in room temperature under batch equilibrium model. The equilibrium data for adsorption of fluoride on the synthesized blends were well represented by the Freundlich isotherm, giving a maximum adsorption capacity of 17.50mg/g. The adsorption kinetic models were also examined and it was found that all the sorption processes were better described by the pseudo-second-order model. This results suggested that the efficiency of the fluoride removal process was mainly controlled by electrostatic attraction and ion-exchange mechanism. Furthermore, the CS@La-IDAMP material was tested for the regeneration ability with the suitable regenerant to make this process as cost-effective. Finally, it can be concluded that the composite material is the potential adsorbent for the treatment of fluoride from water.

Enhancement of oil recovery using zirconium-chitosan hybrid composite by adsorptive method.

Recovery of oil from oil-in-water emulsion has been investigated by many scientists and it continues to be a challenging task for environmental scientists so far. Among all the techniques, adsorption is found to be an appropriate process for the removal of oil from oil-in-water emulsion owing to its high efficiency and easy operation. A hybrid material, zirconium-chitosan composite (Zr-CS-HC) was prepared to remove the oil from oil-in-water emulsion and oil was measured by extractive gravimetric method. Various parameters viz., agitation time, pH, sorbent dosage and initial oil concentration for maximum sorption were optimized. In this study, the maximum oil removal percentage was found to be at pH 3.0 and a minimum contact time of 50min using prepared sorbent. The pH of the sorption studies revealed that oil sorption was favored in acidic condition. The sorbent was characterized using FTIR, SEM with EDAX, XRD, TGA and DSC; contact angle and heat of combustion. The experimental data were explained using Freundlich, Langmuir, D-R and Tempkin isotherms to find the best fit for the sorption process. Thermodynamic parameters such as ΔG°, ΔH° and ΔS° were calculated to understand the nature of sorption process. This work provides a potential platform for the expansion of oil removal technology.

Recovery of oil from oil-in-water emulsion using biopolymers by adsorptive method.

In the present study, it is aimed to identify, a low cost sorbent for the recovery of oil from oil-in-water emulsion using biopolymers such as chitin and chitosan. Chitin has the greater adsorption capacity than chitosan due to its hydrophobic nature. The characterizations of chitin and chitosan were done using FTIR, SEM, EDAX, XRD, TGA and DSC techniques. Under batch equilibrium mode, a systematic study was performed to optimize the various equilibrium parameters viz., contact time, pH, dosage, initial concentration of oil, and temperature. The adsorption process reached equilibrium at 40 min of contact time and the percentage removal of oil was found to be higher (90%) in the acidic medium. The Freundlich and Langmuir models were applied to describe the equilibrium isotherms and the isotherm constants were calculated. Thermodynamic parameters such as ΔG°, ΔH° and ΔS° were calculated to find out the nature of the sorption mechanism. The kinetic studies were investigated with reaction-based and diffusion-based models. The suitable mechanism for the removal of oil has been established.