Valorization of date palm leaves for adsorptive remediation of 2,4-dichlorophenoxyacetic acid herbicide polluted agricultural runoff.

Alarming rates of water contamination by toxic herbicides have prompted the need and attention for easy, efficient, and affordable treatment options with a touch of circular economy aspects. This study valorized date palm leaf (DPL) wastes into a valuable adsorbent for remediating agricultural wastewater polluted with 2,4-Dichlorophenoxyacetic acid (2,4-DPA) herbicide. The DPL precursor was modified with H2SO4 treatment and both biomass samples were characterized by various analytical techniques. Acid treatment modified the morphology, thermal, and textural properties of the final product (TDPL) while maintaining the structure and surface chemistry intact. Simulated wastewaters containing 2,4-DPA were subsequently treated using TDPL as an adsorbent. Optimum adsorption conditions of pH 2, dosage 0.95 g/L, shaking speed 200 rpm, time 120 min, and temperature 30 °C showed a good herbicide removal efficiency in the range of 55.1-72.6% for different initial feed concentrations (50-250 mg/L). Experimental kinetic data were better represented by the pseudo-second-order model, while the Freundlich isotherm was reliable in describing the equilibrium behavior of the adsorption system. Further, the thermodynamic analysis revealed that the adsorption occurred spontaneously, favorably, and exothermically. Plausible sorption mechanism involved electrostatic interactions, weak van der Waals forces, hydrogen bonds, and π-π interactions between the participating phases. Conspicuously, TDPL application to real-world situations of treating actual herbicide-polluted agricultural runoff resulted in a 69.4% remediation efficiency. Thus, the study demonstrated the valorization of date palm leaves into a valuable and industry-ready adsorbent that can sequester toxic 2,4-DPA herbicide contaminant from aqueous streams.

Phycoremediation for carbon neutrality and circular economy: Potential, trends, and challenges.

Phycoremediation is gaining attention not only as a pollutant mitigation approach but also as one of the most cost-effective paths to achieve carbon neutrality. When compared to conventional treatment methods, phycoremediation is highly effective in removing noxious substances from wastewater and is inexpensive, eco-friendly, abundantly available, and has many other advantages. The process results in valuable bioproducts and bioenergy sources combined with pollutants capture, sequestration, and utilization. In this review, microalgae-based phycoremediation of various wastewaters for carbon neutrality and circular economy is analyzed scientometrically. Different mechanisms for pollutants removal and resource recovery from wastewaters are explained. Further, critical parameters that influence the engineering design and phycoremediation performance are described. A comprehensive knowledge map highlighting the microalgae potential to treat a variety of industrial effluents is also presented. Finally, challenges and future prospects for industrial implementation of phycoremediation towards carbon neutrality coupled with circular economy are discussed.

Fabrication of Ru-CoFe2O4/RGO hierarchical nanostructures for high-performance photoelectrodes to reduce hazards Cr(VI) into Cr(III) coupled with anodic oxidation of phenols.

Dual-functional photo (electro)catalysis (PEC) is a key strategy for removing coexisting heavy metals and phenolic compounds from wastewater treatment systems. To design a PEC cell, it is crucial to use chemically stable and cost-effective bifunctional photocatalysts. The present study shows that ruthenium metallic nanoparticles decorated with CoFe2O4/RGO (Ru-CoFe2O4/RGO) are effective bifunctional photoelectrodes for the reduction of Cr(VI) ions. Ru-CoFe2O4/RGO achieves a maximum Cr(VI) reduction rate of 99% at 30 min under visible light irradiation, which is much higher than previously reported catalysts. Moreover, PEC Cr(VI) reduction rate is also tuned by adding varying concentration of phenol. A mechanism for the concurrent removal of Cr(VI) and phenol has been revealed over a bifunctional Ru-CoFe2O4/RGO catalyst. A number of key conclusions emerged from this study, demonstrating the dual role of phenol during Cr(VI) reduction by PEC. Anodic oxidation of phenol produces the enormous H+ ion, which appears to be a key component of Cr(VI) reduction. Additionally, phenolic molecules serve as hole (h+) scavengers that reduce e-/h+ recombination, thus enhancing the reduction rate of Cr(VI). Therefore, the Ru-CoFe2O4/RGO photoelectrode exhibits a promising capability of reducing both heavy metals and phenolic compounds simultaneously in wastewater.

Nanochitosan/carboxymethyl cellulose/TiO2 biocomposite for visible-light-induced photocatalytic degradation of crystal violet dye.

Development of novel bionanomaterials for water and wastewater treatment has gained increased attraction and attention in recent times. The present study reports an effective biocomposite-based nano-photocatalyst comprised of nanochitosan (NCS), carboxymethyl cellulose (CMC), and titanium dioxide (TiO2) synthesized by sol-gel technique. The as-prepared NCS/CMC/TiO2 photocatalyst was systematically characterized by X-ray diffraction, Fourier Transform Infrared spectroscopy, Scanning Electron Microscopy with energy dispersive X-beam spectroscopy, Differential scanning calorimetry (DSC), and Thermogravimetric analysis (TGA). Photocatalytic degradation of the crystal violet (CV) dye using this nano photocatalyst was studied by varying the irradiation time, catalyst dosage, feed pH, and initial dye concentration. Further, the kinetic analysis of dye degradation was explored using the Langmuir-Hinshelwood model, and a plausible photocatalytic mechanism was proposed. The modification of TiO2 using NCS and CMC accelerated photocurrent transport by increasing the number of photogenerated electrons and holes. Overall, the study indicated the excellent photocatalytic performance of 95% CV dye degradation by NCS/CMC/TiO2 than the bare inorganic TiO2 photocatalyst under visible light irradiation.

Silver-sepiolite (Ag-Sep) hybrid reinforced active gelatin/date waste extract (DSWE) blend composite films for food packaging application.

In this study, date syrup waste extract (DSWE) (15 wt%) and different content of silver doped sepiolite hybrid (Ag-Sep, 0.25-3 wt%) were incorporated into gelatin matrix to develop a series of active composite packaging films. Incorporating 2 wt% of Ag-Sep increased the modulus of blend film by 98% compared to unmodified gelatin/DSWE blend film. The active gelatin composite film exhibited superior active compounds migration to aqueous food simulants. Besides, Ag-Sep provided a tortuous pathway to the composite film, resulting in high 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical inhibition efficiency (91%) and slow-release kinetics of active compounds to the food simulant. The Ag-Sep hybrid was improved the antimicrobial property of the gelatin/DSWE blend film against both gram-negative and gram-positive microbes. Thus, this study demonstrated that the Ag-Sep hybrid exhibits significant properties in the active gelatin composite films, implying that this hybrid could be an effective additive for various active packaging films.

A review of the therapeutic and biological effects of edible and wild mushrooms.

Throughout history, mushrooms have occupied an inseparable part of the diet in many countries. Mushrooms are considered a rich source of phytonutrients such as polysaccharides, dietary fibers, and other micronutrients, in addition to various essential amino acids, which are building blocks of vital proteins. In general, mushrooms offer a wide range of health benefits with a large spectrum of pharmacological properties, including antidiabetic, antioxidative, antiviral, antibacterial, osteoprotective, nephroprotective, hepatoprotective, etc. Both wild edible and medicinal mushrooms possess strong therapeutic and biological activities, which are evident from their in vivo and in vitro assays. The multifunctional activities of the mushroom extracts and the targeted potential of each of the compounds in the extracts have a broad range of applications, especially in the healing and repair of various organs and cells in humans. Owing to the presence of the aforementioned properties and rich phytocomposition, mushrooms are being used in the production of nutraceuticals and pharmaceuticals. This review aims to provide a clear insight on the commercially cultivated, wild edible, and medicinal mushrooms with comprehensive information on their phytochemical constituents and properties as part of food and medicine for futuristic exploitation. Future outlook and prospective challenges associated with the cultivation and processing of these medicinal mushrooms as functional foods are also discussed.

Valorization of groundnut shell via pyrolysis: Product distribution, thermodynamic analysis, kinetic estimation, and artificial neural network modeling.

Pyrolysis of agricultural biomass is a promising technique for producing renewable energy and effectively managing solid waste. In this study, groundnut shell (GNS) was processed at 500 °C in an inert gas atmosphere with a gas flow rate and a heating rate of 10 mL/min and 10 °C/min, respectively, in a custom-designed fluidized bed pyrolytic-reactor. Under optimal operating conditions, the GNS-derived pyrolytic-oil yield was 62.8 wt.%, with the corresponding biochar (19.5 wt.%) and biogas yields (17.7 wt.%). The GC-MS analysis of the GNS-based bio-oil confirmed the presence of (trifluoromethyl)pyridin-2-amine (18.814%), 2-Fluoroformyl-3,3,4,4-tetrafluoro-1,2-oxazetidine (16.23%), 5,7-dimethyl-1H-Indazole (11.613%), N-methyl-N-nitropropan-2-amine (6.5%) and butyl piperidino sulfone (5.668%) as major components, which are used as building blocks in the biofuel, pharmaceutical, and food industries. Furthermore, a 2 × 5 × 1 artificial neural network (ANN) architecture was developed to predict the decomposition behavior of GNS at heating rates of 5, 10, and 20 °C/min, while the thermodynamic and kinetic parameters were estimated using a non-isothermal model-free method. The Popescu method predicted activation energy (Ea) of GNS biomass ranging from 111 kJ/mol to 260 kJ/mol, with changes in enthalpy (ΔH), Gibbs-free energy (ΔG), and entropy (ΔS) ranging from 106 to 254 kJ/mol, 162-241 kJ/mol, and -0.0937 to 0.0598 kJ/mol/K, respectively. The extraction of high-quality precursors from GNS pyrolysis was demonstrated in this study, as well as the usefulness of the ANN technique for thermogravimetric analysis of biomass.

Nano-activated carbon derived from date palm coir waste for efficient sequestration of noxious 2,4-dichlorophenoxyacetic acid herbicide.

Alarming water contamination rates by toxic herbicides have drawn attention to treat these pollutants using efficient, easy, and economic techniques. In this work, date-palm coir (DPC) waste-based nano-activated carbon (DPC-AC) was successfully prepared and examined for adsorptive removal of toxic 2,4-dichlorophenoxyacetic acid (2,4-DPA) herbicide from synthetic wastewater. The DPC-AC was synthesized via a single-step carbonization-KOH activation approach. The nanosorbent displayed a flaky morphology with graphitic structure and oxygen-rich surface functionalities. The nanocarbon with a mean particle size of 163 nm possessed a high specific surface area of 947 m2/g with an average pore size of 2.28 nm. High 2,4-DPA removal efficiency of 98.6% was obtained for the optimal adsorption conditions of pH 2, dosage 0.15 g, rotational speed 100 rpm, time 90 min, and initial 2,4-DPA concentration of 100 mg/L. Langmuir isotherm best described the equilibrium behavior with a theoretical maximum of 50.25 mg/g adsorption capacity for the system. Pseudo-second order model was more appropriate in quantifying the kinetics for all initial feed concentrations. Thermodynamically, the adsorption process was spontaneous, endothermic, and involved low activation energy. A plausible mechanism for the adsorption-desorption of 2,4-DPA onto DPC-AC is also discussed. Cost analysis and regenerability studies proved the economic value ($3/kg) and reusable nature of DPC-AC without any significant loss in its performance. Overall, this study highlights the advantages of DPC waste valorization into efficient nanoadsorbent and the sequestration of noxious 2,4-DPA herbicide from its aqueous streams using this nanosorbent.

Adsorptive removal of noxious atrazine using graphene oxide nanosheets: Insights to process optimization, equilibrium, kinetics, and density functional theory calculations.

Atrazine is a toxic herbicide whose alarming rate of contamination in the drinking water and wastewater poses a severe threat to the environment and human health. Here in this study, the graphene oxide (GO) nanosheets were prepared using Hummers' method with minor modification and studied as a potential adsorbent for atrazine removal from simulated wastewater. The spectroscopy and microscopic analysis confirmed the successful formation of GO with a multilayer structure resembling the crumpled sheets with random stacking. The Response Surface Methodology (RSM) employing Box Behnken design (BBD) was successfully developed to predict the optimal conditions for maximal atrazine removal as adsorbent dosage 121.45 mg/L; initial feed concentration 27.03 mg/L; temperature 27.69 °C, pH 5.37, and time 180 min. The atrazine adsorption onto GO was found to be higher in acidic pH and lower temperature. Density functional theory (DFT) calculation of adsorbent-adsorbate complex in the implicit solvent medium suggests adsorption affinity energy of -24.4 kcal/mol for atrazine. A careful observation of the molecules configuration and binding energy showed that the π-π interactions and hydrogen bonds played a significant role in the adsorption phenomena. Langmuir isotherm suited well to the adsorption process with a maximum adsorption capacity of 138.19 mg/g, at 318 K. The fitness of kinetic models for atrazine adsorption onto GO nanosheets were in following order Ho < Sobkowsk-Czerwi < Avrami model based on their correlation coefficient (R2) values. Reusability analysis showed that GO nanosheets could be effectively recycled using 0.01 N NaOH up to six cycles of atrazine removal. Thus, this study provided a theoretical and experimental basis for the potential application of GO nanosheets as a novel adsorbent for the removal of hazardous atrazine.

Hybrid capacitive deionization of NaCl and toxic heavy metal ions using faradic electrodes of silver nanospheres decorated pomegranate peel-derived activated carbon.

Capacitive deionization (CDI) is an evolving technology for eradicating salt and toxic heavy metal ions from brackish wastewater. However, traditional CDI electrodes have lower salt adsorption capacity and inadequate adsorption of selective metal ions for long-term operations. Herein, Ag nanospheres incorporated pomegranate peel-derived activated carbon (Ag/P-AC) was prepared and implied to the CDI process for removing NaCl, toxic mono-, di-, and trivalent metal ions. Morphological analysis revealed that the 80-100 nm-sized Ag nanospheres were uniformly decorated on the surfaces of P-AC nanosheets. The Ag/P-AC has a higher specific surface area (640 m2 g-1), superior specific capacitance (180 F g-1 at 50 mV s-1) and a lower charge transfer resistance (0.5 Ω cm2). CDI device was fabricated by Ag/P-AC as an anode, which adsorbed anions and P-AC as cathode for adsorption of positively charged ions at 1.2 V in an initial salt concentration of 1000 mg L-1. An asymmetric Ag/P-AC//P-AC exhibited a maximum NaCl adsorption capacity of 36 mg g-1 than symmetric P-AC//P-AC electrodes (22.7 mg g-1). Furthermore, Pb(II), Cd(II), F-, and As(III) ions were successfully removed from simulated wastewater by using Ag/P-AC//P-AC based CDI system. These asymmetric CDI-electrodes have an excellent prospect for the removal of salt and toxic contaminants in industrial wastewater.

Synthesis of TiO2/RGO with plasmonic Ag nanoparticles for highly efficient photoelectrocatalytic reduction of CO2 to methanol toward the removal of an organic pollutant from the atmosphere.

The synergistic photoelectrochemical (PEC) technology is a robust process for the conversion of CO2 into fuels. However, designing a highly efficient UV-visible driven photoelectrocatalyst is still challenging. Herein, a plasmonic Ag NPs modified TiO2/RGO photoelectrocatalyst (Ag-TiO2/RGO) has been designed for the PEC CO2 reduction into selective production of CH3OH. HR-TEM analysis revealed that Ag and TiO2 NPs with average sizes of 4 and 7 nm, respectively, were densely grown on the few-micron-sized 2D RGO nanosheets. The physicochemical analysis was used to determine the optical and textural properties of the Ag-TiO2/RGO nanohybrids. Under VU-Vis light illumination, Ag-TiO2/RGO photocathode possessed a current density of 23.5 mA cm-2 and a lower electrode resistance value of 125 Ω in CO2-saturated 1.0 M KOH-aqueous electrolyte solution. Catalytic studies showed that the Ag-TiO2/RGO photocathode possessed a remarkable PEC CO2 reduction activity and selective production of CH3OH with a yield of 85 µmol L-1 cm-2, the quantum efficiency of 20% and Faradic efficiency of 60.5% at onset potential of -0.7 V. A plausible PEC CO2 reduction mechanism over Ag-TiO2/RGO photocathode is schematically demonstrated. The present work gives a new avenue to develop high-performance and stable photoelectrocatalyst for PEC CO2 reduction towards sustainable liquid fuels production.

Effect of date fruit waste extract as an antioxidant additive on the properties of active gelatin films.

In this work, date-fruit syrup waste extract (DSWE) was used as an antioxidant additive to develop active gelatin films with enhanced food preservation properties. The effect of DSWE content (5, 10, 15, and 25 wt%) on the mechanical, physical, and antioxidant properties of the gelatin films were analyzed. Total phenolic content and antioxidant assay analysis revealed that the active compounds in blend films are highly migrated to the aqueous phase than the fatty medium. In the canola oil stability studies, gelatin/25 wt% DSWE film immersed oil sample exhibited low peroxide (POV) and p-anisidine (PV) values of 28.6 and 7.1, respectively, compared to the control oil (POV = 41.7 and PV = 13.1) in the air atmosphere and 45 °C for 30 days. Totox values of canola oil samples were decreased as a function of DSWE content in the films, indicating that polyphenols in DSWE are significantly resistant to oil's lipid oxidation.

Surface functionalized highly porous date seed derived activated carbon and MoS2 nanocomposites for hydrogenation of CO2 into formic acid.

In recent years, substantial progress has been made towards developing effective catalysts for the hydrogenation of CO2 into fuels. However, the quest for a robust catalyst with high activity and stability still remains challenging. In this study, we present a cost-effective catalyst composed of MoS2 nanosheets and functionalized porous date seed-derived activated carbon (f-DSAC) for hydrogenation of CO2 into formic acid (FA). As-fabricated MoS2/f-DSAC catalysts were characterized by FE-SEM, XRD, Raman, FT-IR, BET, and CO2-TPD analyses. At first, bicarbonate (HCO3-) was successfully converted into FA with a high yield of 88% at 200 °C for 180 min under 10 bar H2 atmosphere. A possible reaction pathway for the conversion of HCO3- into FA is postulated. The catalyst has demonstrated high activity and long-term stability over five consecutive cycles. Additionally, MoS2/f-DSAC catalyst was effectively used for the conversion of gaseous CO2 into FA at 200 °C under 20 bar (CO2/H2 = 1:1) over 15 h. The catalyst exhibited a remarkable TOF of 510 h-1 with very low activation energy of 12 kJ mol-1, thus enhancing the catalytic conversion rate of CO2 into FA. Thus, this work demonstrates the MoS2/f-DSAC nanohybrid system as an efficient non-noble catalyst for converting CO2 into fuels.

Improved permeability and antifouling performance of polyethersulfone ultrafiltration membranes tailored by hydroxyapatite/boron nitride nanocomposites.

To extend the use of polyethersulfone (PES) ultrafiltration membranes in water process engineering, the membrane's wettability and anti-fouling properties should be further improved. In this context, hydroxyapatite/boron nitride (HAp/BN) nanocomposites have been prepared and intercalated into PES membranes using a non-solvent-induced phase separation process. High-quality 2D transparent boron nitride nanosheets (BN NSs) were prepared using an environmentally friendly and green-template assisted synthesis method in which 1D hexagonal hydroxyapatite nanosheets (HAp NRs) were uniformly distributed and hydrothermally immobilized at 180 °C. SEM, XRD, and Raman spectroscopy techniques were used to characterize the HAp/BN nanocomposites. PES membranes intercalated with various nanocomposite amounts (0-4 wt %) were also characterized by permeability, porosity, and contact angle measurements. Additional pathways for water molecule transport were promoted by the high surface area of the BN NSs, resulting in high permeability. Membrane wettability and antifouling properties were also improved by the inclusion of negative charge groups (OH- and PO43-) on HAp. Hybrid membranes containing 4 wt% HAp/BN showed the best overall performance with ∼97% increase in water flux, 90% rejection of bovine serum albumin (BSA), high water flux recovery ratio, low irreversible fouling, and high reversible fouling pattern. The intercalation of HAp/BN with the PES matrix therefore opens up a new direction to enhance the PES UF membranes' hydrophilicity, water flux, and antifouling capacity.

Ultrasound in the deproteinization process for chitin and chitosan production.

Recently, chitin and chitosan are widely investigated for food preservation and active packaging applications. Chemical, as well as biological methods, are usually adopted for the production of these biopolymers. In this study, modification to a chemical method of chitin synthesis from shrimp shells has been proposed through the application of high-frequency ultrasound. The impact of sonication time on the deproteinization step of chitin and chitosan preparation was examined. The chemical identities of chitin and chitosan were verified using infrared spectroscopy. The influence of ultrasound on the deacetylation degree, molecular weight and particle size of the biopolymer products was analysed. The microscopic characteristics, crystallinity and the colour characteristics of the as-obtained biopolymers were investigated. Application of ultrasound for the production of biopolymers reduced the protein content as well as the particle size of chitin. Chitosan of high deacetylation degree and medium molecular weight was produced through ultrasound assistance. Finally, the as-derived chitosan was applied for beef preservation. High values of luminosity, chromatid and chrome were noted for the beef samples preserved using chitosan films, which were obtained by employing biopolymer subjected to sonication for 15, 25 and 40 min. Notably; these characteristics were maintained even after ten days of packaging. The molecular weight of these samples are 73.61 KDa, 86.82 KDa and 55.66 KDa, while the deacetylation degree are 80.60%, 92.86% and 94.03%, respectively; in the same order, the particle size of chitosan are 35.70 µm, 25.51 µm and 20.10 µm.

Green synthesis of zinc oxide nanoparticles using Phoenix dactylifera waste as bioreductant for effective dye degradation and antibacterial performance in wastewater treatment.

Production of multi-functional zinc oxide nanoparticles (ZnO-NPs) for wastewater treatment through green-approaches is a desirable alternative for conventional synthesis routes. Biomass waste valorization for nanoparticles synthesis has received increased research attention. The present study reports date pulp waste (DPW) utilization as an effective bio-reductant for green-synthesis of ZnO-NPs. A simple and eco-friendly process with low reaction time and calcination temperature was adopted for DPW mediated ZnO-NPs (DP-ZnO-NPs) synthesis. Microscopic investigations of DP-ZnO-NPs confirmed the non-agglomeration and spherical nature of particles with mean diameter of 30 nm. EDX and XPS analysis defined the chemical composition and product purity of DP-ZnO-NPs. UV and photoluminescence studies exhibited surface plasmonic resonance at 381 nm and fluorescent nature of DP-ZnO-NPs. FTIR studies established a formation mechanism outline for DP-ZnO-NPs. XRD and Raman investigations confirmed the crystalline and hexagonal wurtzite phase of DP-ZnO-NPs. DSC/TG analysis displayed the thermal stability of DP-ZnO-NPs with <10 wt% loss upto 700 °C. Photocatalytic degradation of hazardous methylene blue and eosin yellow dyes using DP-ZnO-NPs, showed rapid decomposition rate with 90 % degradation efficiency. Additionally, DP-ZnO-NPs demonstrated significant antibacterial effects on various pathogenic bacteria in terms of zone-of-inhibition measured by disc-diffusion method. Thus, the as-prepared DP-ZnO-NPs is suitable for industrial wastewater treatment.

Augmented biohydrogen production from rice mill wastewater through nano-metal oxides assisted dark fermentation.

This study highlights biohydrogen production enrichment through NiO and CoO nanoparticles (NPs) inclusion to dark fermentation of rice mill wastewater using Clostridium beijerinckii DSM 791. NiO (~26 nm) and CoO (~50 nm) NPs were intrinsically prepared via facile hydrothermal method with polyhedral morphology and high purity. Dosage dependency studies revealed the maximum biohydrogen production characteristics for 1.5 mg/L concentration of both NPs. Biohydrogen yield was improved by 2.09 and 1.9 folds higher for optimum dosage of NiO and CoO respectively, compared to control run without NPs. Co-metabolites analysis confirmed the biohydrogen production through acetate and butyrate pathways. Maximum COD reduction efficiencies of 77.6% and 69.5% were observed for NiO and CoO inclusions respectively, which were higher than control run (57.5%). Gompertz kinetic model fitted well with experimental data of NPs assisted fermentation. Thus, NiO and CoO inclusions to wastewater fermentation seems to be a promising technique for augmented biohydrogen production.

Designed assembly of Ni/MAX (Ti3AlC2) and porous graphene-based asymmetric electrodes for capacitive deionization of multivalent ions.

The contamination of aquatic ecosystems by fluoride and heavy metal ions constitute an environmental hazard and has been proven to be harmful to human health. This study explores the feasibility of using asymmetric capacitive deionization (CDI) electrodes to remove such toxic ions from wastewater. An asymmetric CDI cell was fabricated using 2D Ni/MAX as an anode and 3D porous reduced graphene oxide (pRGO) as a cathode for the electrosorption of F-, Pb2+, and As(III) ions. A simple microwave process was used for the synthesis of Ni/MAX composite using fish sperm DNA (f-DNA) as a cross-linker between MAX nanosheets (NSs) and the metallic Ni nanoparticles (NPs). Further, pRGO anode was prepared through effective reduction of RGO using lemon juice as green reducing agent with the assist of f-DNA as a structure-directing agent for the formation of 3D network. With this tailored nanoarchitecture, pRGO and Ni/MAX electrodes exhibited a high specific capacitance of 760 and 385 F g-1, respectively. The fabricated Ni/MAX and pRGO based CDI system demonstrated a high electrosorption capacity of 68, 76, and 51 mg g-1 for the monovalent F-, divalent Pb2+, and trivalent As(III) ions at 1.4 V in neutral pH. Furthermore, Ni/MAX//pRGO system was successfully applied for the removal of total F(T), Pb(T), and As(T) ions from real industrial wastewater and contaminated groundwater. The present findings indicate that the fabricated Ni/MAX//pRGO electrode has excellent electrochemical properties that can be exploited for the removal of anionic and cationic metal ions from aqueous solutions in a CDI based system.

Biosorption potential of Phoenix dactylifera coir wastes for toxic hexavalent chromium sequestration.

Valorization of waste phytomass into valuable components provide new functionality to these biowastes and annul problems associated with their safe disposal. In this study, date palm (Phoenix dactylifera) coir (DPC) waste was tested for its toxic hexavalent chromium (Cr(VI)) ions biosorption. The DPC biosorbent was subjected to SEM, EDX, FTIR, TGA and N2 adsorption/desorption characterization studies. Results showed that the cellulose-rich DPC surface contained mesopores with a wide number of functional groups and possessed suitable surface attributes for Cr(VI) ions sequestration. Batch biosorption tests established the Cr(VI) ions sequestration potential of the DPC biosorbent with a maximum chromium removal efficiency of 87.2% for a 100 ppm initial feed concentration at pH 2, dosage 0.3 g, temperature 30 °C, contact time 60 min and agitation speed 100 rpm. Langmuir isotherm fitted well (R2 = 0.9955) with the experimental data while the kinetic analysis showed that Cr(VI) ions sequestration by DPC followed the pseudo-second order model. Biosorption thermodynamics revealed the exothermic nature and low-temperature preference for the effective binding of chromium ions on DPC. Regeneration of the biosorbent using NaOH wash showed a nearly steady Cr(VI) ions removal efficiency (with a loss <10%) by the DPC till four recycle runs. Economic analysis showed a very low production cost of $1.09/kg for the DPC biosorbent with a total cost of $4.36/m3 for a scale-up batch process wastewater treatment plant. Thus, a low-cost, effectual and sustainable biosorbent for effective treatment of Cr(VI) ions polluted water streams has been reported.

WITHDRAWN: Sustainable liquid membrane separation using interfacial engineering of deep eutectic solvent and cellulose acetate.

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