Biodegradable MoNx@Mo-foil electrodes for human-friendly supercapacitors.

With the advancement in the field of biomedical research, there is a growing demand for biodegradable electronic devices. Biodegradable supercapacitors (SCs) have emerged as an ideal solution for mitigating the risks associated with secondary surgeries, reducing patient discomfort, and promoting environmental sustainability. In this study, MoNx@Mo-foil was prepared as an active material for biodegradable supercapacitors through high-temperature and nitridation processes. The composite electrode exhibited superior electrochemical performance in both aqueous and solid-state electrolytes. In the case of the solid-state electrolyte, the MoNx@Mo-foil composite electrode-based device demonstrated excellent cycling stability and electrochemical performance. Additionally, the composite electrode exhibited rapid and complete biodegradability in a 3% H2O2 solution. Through detailed experimental analysis and performance testing, we verified the potential application of the MoNx@Mo-foil composite electrode in biodegradable supercapacitors. This work provides a new choice of degradable material for developing biomedical electronic devices.

Evaluating sustainable municipal solid waste management scenarios: A multicriteria decision making approach.

Due to increasing urbanization and population growth, municipal solid waste management (MSWM) is a significant environmental concern in developing countries. Inadequate waste management systems lead to environmental pollution, health hazards, and economic losses. While considering the challenges and limitations, policymakers and authorities need to opt for such waste management scenarios that are environmentally friendly and resolve energy issues. Ten MSWM scenarios were developed and evaluated using seven different criteria. Four multi-criteria decision-making (MCDM) techniques, namely fuzzy logic, AHP, TOPSIS, and PROMETHEE II, were employed to rank the scenarios and identify the most appropriate option for solid waste management in Lahore. This study highlights that the optimal waste management approach comprises a composition of 54% anaerobic digestion, 37% gasification, and 9% landfill technologies. These percentages collectively represent the most suitable and effective strategies for the city's waste management needs. All the MCDM techniques consistently produce similar results. These scenarios have broader applicability across cities in Central Asia and beyond. The study's findings are aligned to promote sustainable and environmentally friendly MSWM practices. These findings endorse implementing strategies and measures aimed at fostering environmental sustainability and the responsible handling of waste, serving as a valuable reference for various regions.

Fabrication of NIPMAM based polymer microgel network assisted rhodium nanoparticles for reductive degradation of toxic azo dyes.

The aim of this study was to prepare poly-N-isopropylmethacrylamide-co-acrylic acid-acrylamide [p-(NIPMAM-co-AA-AAm)] via precipitation polymerization in an aqueous medium. Rhodium nanoparticles were formed in the microgel network by an in-situ reduction technique with the addition of sodium borohydride as a reducing agent. Pure p-(NIPMAM-co-AA-AAm) and hybrid microgels [Rh-(p-NIPMAM-co-AA-AAm)] microgels were examined by using UV-Visible, FTIR (Fourier Transform Infrared), SEM (Scanning Electron Microscopy), TEM (Transmission Electron Microscopy), DLS (Dynamic Light Scattering) and XRD (X-Ray Diffraction) techniques. The catalytic activities of the hybrid microgel [Rh-(p-NIPMAM-co-AA-AAm)] for the degradation of azo dyes such as alizarin yellow (AY), congo red (CR), and methyl orange (MO) were compared and the mechanism of the catalytic action by this system was examined. Various parameters including the catalyst amount and dye concentration influenced the catalytic decomposition of azo dyes. In order to maximize the reaction conditions for the dye's quick and efficient decomposition, the reaction process was monitored by spectroscopic analysis. The rate constants for reductive degradation of azo dyes were measured under various conditions. When kapp values were compared for dyes, it was found that [Rh-(p-NIPMAM-co-AA-AAm)] hybrid microgels showed superior activity for the degradation of MO dyes compared to the reductive degradation of CR and AY.

Valorization of algal biomass to synthesize heterogeneous gC3N4-Biochar photocatalyst for the treatment of industrial wastewater using photocatalysis-persulfate oxidation process.

Textile wastewater, heavily contaminated with organic dyes, is generating severe problems to environment and human health. The implementation of gC3N4 with biochar (gC3N4-BC) for the treatment of textile wastewater is less effective due to the limited adsorption capacity and slower degradation kinetics. To tackle these problems, peroxydisulfate (PDS) is integrated with gC3N4-BC photocatalyst to enhance the process efficiency and kinetics. The synthesized gC3N4-BC-5 composite shows higher separation of charge carriers, light absorbance, and lower energy bandgap (2.62 eV). The results of photocatalytic degradation and rate constant are enhanced up to 99.9 % and 0.041 min-1 using gC3N4-BC-5 with PDS as compared to without PDS (96.8 % and 0.028 min-1, respectively). The radicals (SO4-•,O2-•, and OH•) are responsible to improve the degradation process efficiency and kinetics. The reusability of optimized sample indicates that gC3N4-BC-5 is stable and effective up to five cycles. The gC3N4-BC-5 composite attains highest adsorption (70.9 %) when compared to BC (62.3 %) and pure gC3N4 (27.1 %). The well-fitted models of adsorption (Pseudo-Second-Order and Freundlich) confirm the favorable, chemical, and multilayered adsorption process. The coupling of gC3N4-BC-5 with PDS is effective, efficient, and stable process to enhance the kinetics and degradation of textile wastewater.

Prediction study of structural, electronic and optical properties of 4C16H10Br2O2 Bis (m-bromobenzoyl) methane crystals.

By first-principles calculations with density functional theory and a pseudopotential approach, the structural, electronic, and optical properties of the anhydrous 4C16H10Br2O2 Bis (2-Bromobenzoyl) Methane crystals in Pbnc (N°60) and P21/c (N°14) space group are investigated. All computations are determined by a generalized gradient approximation, local density approximation and an ultra-soft pseudopotential. The calculated equilibrium parameters are in good agreement with their available experimental data. This calculation shows that the GGA/PW91 functional overestimate the lattice constant, unlike the LDA/CA-PZ. The Br-C bond distance of 1.856 (1.902) Å is comparable with experimental value of 1.901 (1.896) Å in Pbnc (P21/c) space groups. The direct band gap nature is obtained for both space groups Pbnc and P21/c, since the maximum of the valence band and the minimum of the conduction band are both situated at the YA center.

Evaluation on microalgae for the production of bio-chemicals and electricity.

Recent advancement in biophotovoltaic systems using microalgae, coupled with biorefinery approach, would improve economy-feasibility in production. The major concern is its commercial strength in terms of scalability, strain selection and extraction procedure cost. It must compete with conventional feedstocks such as fossil fuels. This project proposes to enhance the economic feasibility of microalgae-based biorefinery by evaluating their performance for bio-electricity, bio-diesel and carotenoids production in a single cycle. The first part of the study was to construct and select a Bio-bottle Voltaic (BBV) device that would allow microalgae to grow and produce bioproducts, as well as generate the maximum current output reading derived from the microalgae's photosynthesis process. The second phase consisted of a 25-day investigation into the biorefinery performance of six different microalgal species in producing bio-electricity, bio-diesel and carotenoid in a prototype BBV device. The prototype BBV device with aluminium foil and pencil lead as its anode and cathode produced the highest carotenoid and biodiesel component production from the two microalgae tested, according to the results of the first phase of the experiment. In the second portion of the study, Scenedesmus dimorphus and Chlorella vulgaris were identified as the two microalgae most capable of maintaining their growth throughout the experiment. The maximum current reading observed for C. vulgaris was 653 mV. High Performance Liquid Chromatography analysis showed four major carotenoid compounds found which were Neoxanthin, Cantaxanthin, Astaxanthin and 9-cis antheraxanthin, and the highest carotenoid producer was C. vulgaris which recorded at 1.73 µg/mL. C. vulgaris recorded as the most alkanes producer with 22 compounds detected and Heptacosane and Heneicosane as the two major biodiesel compounds found in the extracts. Evaluation of C. vulgaris data showed that it has enormous potential for microalgal biorefinery candidates. Further ongoing research and development efforts for C. vulgaris will improve the economic viability of microalgae-based industries and reduce reliance on depleted fossil fuels.

Ultrafiltration membrane fabricated from polyethylene terephthalate plastic waste for treating microalgal wastewater and reusing for microalgal cultivation.

Current study had made a significant progress in microalgal wastewater treatment through the implementation of an economically viable polyethylene terephthalate (PET) membrane derived from plastic bottle waste. The membrane exhibited an exceptional pure water flux of 156.5 ± 0.25 L/m2h and a wastewater flux of 15.37 ± 0.02 L/m2h. Moreover, the membrane demonstrated remarkable efficiency in selectively removing a wide range of residual parameters, achieving rejection rates up to 99%. The reutilization of treated wastewater to grow microalgae had resulted in a marginal decrease in microalgal density, from 10.01 ± 0.48 to 9.26 ± 0.66 g/g. However, this decline was overshadowed by a notable enhancement in lipid production with level rising from 181.35 ± 0.42 to 225.01 ± 0.11 mg/g. These findings signified the membrane's capacity to preserve nutrients availability within the wastewater; thus, positively influencing the lipid synthesis and accumulation within microalgal cells. Moreover, the membrane's comprehensive analysis of cross-sectional and surface topographies revealed the presence of macropores with a highly interconnected framework, significantly amplifying the available surface area for fluid flow. This exceptional structural attribute had substantially contributed to the membrane's efficacy by facilitating superior filtration and separation process. Additionally, the identified functional groups within the membrane aligned consistently with those commonly found in PET polymer, confirming the membrane's compatibility and efficacy in microalgal wastewater treatment.

Silver Nanoparticles Decorated with Curcumin Enhance the Efficacy of Metformin in Diabetic Rats via Suppression of Hepatotoxicity.

Hepatotoxicity is one of the significant side effects of chronic diabetes mellitus (DM) besides nephrotoxicity and pancreatitis. The management of this disease is much dependent on the restoration of the liver to its maximum functionality, as it is the central metabolic organ that gets severely affected during chronic diabetes. The present study investigates if the silver nanoparticles decorated with curcumin (AgNP-Cur) can enhance the efficacy of metformin (a conventional antidiabetic drug) by countering the drug-induced hepatoxicity. Swiss albino rats were categorized into six treatment groups (n = 6): control (group I without any treatment), the remaining five groups (group II, IV, V, VI) were DM-induced by streptozocin. Group II was untreated diabetic positive control, whereas groups III was administered with AgNP-cur (5 mg/kg). Diabetic group IV treated with metformin while V and VI were treated with metformin in a combination of the two doses of NPs (5 and 10 mg/kg) according to the treatment schedule. Biochemical and histological analysis of blood and liver samples were conducted after the treatment. The groups V and VI treated with the combination exhibited remarkable improvement in fasting glucose, lipid profile (HDL and cholesterol), liver function tests (AST, ALT), toxicity markers (GGT, GST and LDH), and redox markers (GSH, MDA and CAT) in comparison to group II in most of the parameters. Histological evaluation and comet assay further consolidate these biochemical results, pleading the restoration of the cellular structure of the target tissues and their nuclear DNA. Therefore, the present study shows that the NPs can enhance the anti-diabetic action by suppression of the drug-mediated hepatoxicity via relieving from oxidative stress, toxic burden and inflammation.

Cobalt ferrite/semiconducting single-walled carbon nanotubes based field-effect transistor for determination of carbamate pesticides.

Carbaryl and carbofuran are the carbamate pesticides which have been widely used worldwide to control insects in crops and house. If the pesticides entered in to the food products and drinking water, they could cause serious health effects in humans. Therefore, the development of a rapid, simple, sensitive and selective analytical device for on-site detection of carbamates is crucial to evaluate food and environmental samples. Recently, semiconducting single-walled carbon nanotube-based field effect transistors (s-SWCNT/FETs) have shown several advantages such as high carrier mobility, good on/off ratio, quasi ballistic electron transport, label-free detection and real-time response. Herein, cobalt ferrite (CFO) nanoparticles decorated s-SWCNTs have been prepared and used to bridge the source and drain electrodes. As-prepared CFO/s-SWCNT/FET had been used for the non-enzymatic detection of carbaryl and carbofuran. When used as a sensing platform, the CFO/s-SWCNT hybrid film exhibited high sensitivity, and selectivity with a wide linear range of detection from 10 to 100 fMand the lowest limit of detections for carbaryl (0.11 fM) and carbofuran (0.07 fM) were estimated. This sensor was also used to detect carbaryl in tomato and cabbage samples, which confirmed its practical acceptance. Such performance may be attributed to the oxidation of carbamates by potent catalytic activity of CFO, which led to the changes in the charge transfer reaction on the s-SWCNTs/FET conduction channel. This work presents a novel CFO/s-SWCNT based sensing system which could be used to quantify pesticide residues in food samples.

Photocatalytic Degradation Studies of Organic Dyes over Novel Cu/Ni Loaded Reduced Graphene Oxide Hybrid Nanocomposite: Adsorption, Kinetics and Thermodynamic Studies.

Nowadays, for environmental remediation, photocatalytic process involving graphene-based semiconductors is considered a very promising oxidation process for water treatment. In the present study, nanocomposite (Cu/Ni/rGO) has been synthesized by Dypsis lutescens leaf extract. Characterization of the sample was carried out by UV-visible spectroscopy, scanning electron microscopy (SEM), energy dispersive X-ray (EDX) analysis, Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). Different parameters like contact time, nanocatalyst amount, dye concentration, effect of temperature. and pH factor were optimized to examine the maximum removal efficiency for dyes rhodamine B and alizarine R with and without visible light source. In both cases, i.e., with or without light, maximum removal was observed at 20 mg of nanocatalyst for 5 ppm concentration of both dyes at 45 °C temperature and pH 10 for rhodamine B and pH 4 for alizarine R, respectively with a 20 min contact time. Maximum removal of dyes 93% rhodamine B and 91% alizarine R were observed under a tungsten lamp as compared to without a tungsten lamp, i.e., 78% of RhB and 75% of AR from mixture solution of these dyes. To assess the rate of reaction, spontaneity, and nature of reaction thermodynamics, kinetics and adsorption isotherms were studied. Thermodynamic values indicated that both dyes depicted endothermic and spontaneous degradation processes. Isotherm data fitted best to a Freundlich isotherm, while results of kinetic studies of both dyes followed the pseudo 2nd order kinetic equation. In the end, scavenging radical studies concluded that hydroxyl radicals were the main active specie involved in the photocatalytic degradation process, and regeneration experiments resulted that Cu/Ni/rGO nanocomposites were re-utilized for about four times.

Fabrication of Fe3O4 core-TiO2/mesoSiO2 and Fe3O4 core-mesoSiO2/TiO2 Double Shell Nanoparticles for Methylene Blue Adsorption: Kinetic, Isotherms and Thermodynamic Characterization.

Herein, Fe3O4 core-TiO2/mesoSiO2 and Fe3O4 core-mesoSiO2/TiO2 double shell nanoparticles were prepared by first (R1) and second (R2) routes and applied for the removal of methylene blue. The reported adsorption capacities for R1-0.2, R1-0.4 and R2 samples were 128, 118 and 133 mg.g-1, respectively, which were obtained after 80 min as equilibrium contact time, and pH of 6 using a methylene blue concentration of 200 ppm. The adsorption of methylene blue using the prepared Fe3O4 core-meso SiO2/TiO2 double shell was analyzed by kinetic and isotherms models. In addition, thermodynamic investigations were applied to assess the spontaneous nature of the process. The obtained results confirmed that the pseudo-second order model is well fitted with the adsorption data and the Freundlich-isotherm assumption suggested a multilayer adsorption mechanism. In addition, results of the thermodynamic investigation indicated that ΔG° was in the range of -2.3 to -6.8 kJ/mol for R1-0.2, -2.8 to -6.3 kJ/mol for R1-0.4 and -2.0 to -5.2 kJ/mol for R2. In addition, the ΔH° and ΔS° values were found in the range of 26.4 to 36.19 kJ.mol-1 and 94.9 to 126.3 Jmol-1 K-1, respectively. These results confirm that the surfaces of Fe3O4 core-mesoSiO2/TiO2 and Fe3O4 core-TiO2/mesoSiO2 double shell exhibit a spontaneous tendency to adsorb methylene blue from the aqueous solutions. The achieved performance of Fe3O4 core-meso SiO2/TiO2 and Fe3O4 core-TiO2/meso SiO2 double shell as adsorbent for methylene blue removal will encourage future research investigations on the removal of a broad range of contaminants from wastewater.

Red mud-derived iron carbon catalyst for the removal of organic pollutants in wastewater.

In order to reduce the environmental hazards of red mud (RM) and realize its resource utilization, in this study, RM-based iron-carbon micro-electrolysis material (RM-MEM) were prepared by a carbothermal reduction process using RM as raw material. The influence of the preparation conditions on the phase transformation and structural characteristics of the RM-MEM were investigated during the reduction process. The ability of RM-MEM to remove organic pollutants from wastewater was evaluated. The results showed that RM-MEM prepared at a reduction temperature of 1100 °C, a reduction time of 50 min and a coal dosage of 50% had the best removal effect for the degradation of methylene blue (MB). When the initial MB concentration was 20 mg L-1, the amount of RM-MEM material was 4 g L-1, the initial pH was 7, and the degradation efficiency reached 99.75% after 60 min. When RM-MEM is split into carbon free and iron free parts for use, the degradation effect becomes worse. Compared to other materials, RM-MEM has lower cost and better degradation. X-ray diffraction (XRD) analysis showed that hematite was transformed to zero-valent iron with the increase in the roasting temperature. Scanning electron microscopy (SEM) and energy spectroscopy (EDS) analysis showed that micron-sized ZVI particles were formed in the RM-MEM, and increasing the carbon thermal reduction temperature was beneficial to the growth of zero-valent iron particles.

Investigating the crude oil biodegradation performance in bioreactor by using a consortium of symbiotic bacteria.

Crude oil pollution is one of the most serious environmental issues today, and the clean-up procedure is perhaps the most difficult. Within one to three weeks, the vast majority of oil bacteria may degrade approximately 60% of the crude oil, leaving approximately 40% intact. The by-product metabolites produced during the breakdown of oil are essentially organic molecules in nature. These metabolites inhibit its enzymes, preventing the oil bacteria from further degrading the oil. By combining a variety of different oils with heterotrophic bacteria in a bioreactor, the rate of crude oil biodegradation was accelerated. In this study, two strains of oil-resistant, heterotrophic bacteria (OG1 and OG2-Erythrobacter citreus) and a bacterium that uses hydrocarbons (AR3-Pseudomonas pseudoalcaligenes) were used. Gas chromatography-mass spectroscopy was used to investigate the effectiveness of this consortium of symbiotic bacteria in the biodegradation of crude oil. According to gravimetric and gas chromatography analyses, the consortium bacteria digested 69.6% of the crude oil in the bioreactor, while the AR3 single strain was only able to destroy 61.9% of it. Under the same experimental conditions, consortium bacteria degraded approximately 84550.851 ppb (96.3%) of 16 aliphatic hydrocarbons and 9333.178 ppb (70.5%) of 16 aromatic hydrocarbons in the bioreactor. It may be inferred that the novel consortium of symbiotic bacteria accelerated the biodegradation process and had great potential for use in increasing the bioremediation of hydrocarbon-contaminated locations.

Hydrothermal synthesis of V2O5/TiO2 decorated graphitic carbon nitride nanocomposite for biomolecule oxidation inhibition and dye degradation applications.

Oxides of vanadium, titanium and graphitic carbon nitride (g-C3N4) are well known for their catalytic activities. In order to achieve synergic catalytic effects, a novel nanocomposite (NC) i.e. V2O5/TiO2/g-C3N4 has been synthesized by a very simple, ecofriendly and nonhazardous hydrothermal method. The fabricated NC was characterized employing UV-Visible, FTIR, SEM, and XRD techniques. UV-Visible and FTIR analysis indicated the formation of the nanocomposite and XRD analysis confirmed the association of V2O5 and TiO2 with g-C3N4 in nanocomposite. SEM study indicated the hetero-structure of NC having size ranging from 50 to 80 nm and it was found having hexagonal crystallite structure. The synthesized nanocomposite exhibited excellent scavenging of free radicals DPPH● (91%) and ABTS●+ (64%) that are responsible for the oxidation of biomolecules. Therefore, NC can be claimed having biomolecule oxidation protective potential. In addition, photocatalytic ability for the degradation of methylene blue (MB) and methyl orange (MO) was also achieved up to 94% and 89% respectively. The synthesized novel nanocomposite exhibited excellent potential to remove free radicals and dyes from aqueous medium which can be further used for the environmental remediation.

Biomass derived nitrogen functionalized carbon nanodots for nanomolar determination of levofloxacin in pharmaceutical and water samples.

Binder-free and efficient electrochemical sensing of levofloxacin (LF) was successfully developed based on the nitrogen-doped carbon nanodots (NCNDs). The NCNDs were synthesized by hydrothermal carbonation (180°C for 12 h), and the heteroatom was embedded in aqueous solution of ammonia (NH3). Spectral and microscopic characteristization techniques were used to analyze the topological, crystallinity, and chemical binding behavior of synthesized biomass functional material. HR-TEM image revealed a uniform spherical dot (2.96 nm), and superior quantum yield efficiency (0.42 Φ). The NCNDs was drop coated on a glassy carbon electrode (GCE) and electrochemical sensing of LF was performed by cyclic voltammetry (CV), differential pulse voltammetry (DPV), and amperometric i-t curve in phosphate-buffered saline (PBS; pH = 7.0). The NCNDs modified electrode showed a sharp oxidation peak at +0.95 V (vs. Ag/AgCl) with a four-fold higher current response than the bare GC electrode. The NCNDs/GCE surface not only increases the current response, but has lower detection potential, and facilitates electron transfer reaction. Under optimized working parameters, the NCNDs/GCE showed wide linear concentrations range from 200 nM to 2.8 mM and a low detection limit (LOD) of 48.26 nM (S/N = 3). The electrode modified with NCNDs has high electrochemical sensing stability (RSD = 1.284 ± 0.05% over 5 days), and superior reproducibility (RSD = 1.682 ± 0.06% (n = 3)). Finally, the NCNDs modified GC electrode was successfully applied to quantify the concentration of LF in drug and river water samples with acceptable recovery percentages of 96.60-99.20% and 97.20-99.00% (n=3), respectively.

Thermal Fabrication of Magnetic Fe3O4 (Nanoparticle)@Carbon Sheets from Waste Resources for the Adsorption of Dyes: Kinetic, Equilibrium, and UV-Visible Spectroscopy Investigations.

Thermal treatment is applied for the direct conversion of palm stalk waste to Fe3O4 (np)@carbon sheets (Fe3O4 (np)@CSs). The effect of conversion temperature was investigated. The TEM examination of the prepared magnetic Fe3O4 (np)@CSs showed the formation of Fe3O4 (np) in a matrix of carbon sheets as a coated layer with surface functional groups including carbonyl and hydroxyl groups. Removal of dyes such as methyl orange, methylene blue, and neutral red was achieved using fabricated Fe3O4 (np)@CSs which were prepared at 250 °C, 400 °C, and 700 °C in a weak acidic medium. By studying the contact time effect for the adsorption of methylene blue, neutral red, and methyl orange, using the fabricated Fe3O4 (np)@CSs which were prepared at 250 °C and 400 °C, equilibrium occurred between 120 min and 180 min. In addition, the first-order and second-order kinetic models were applied to the adsorption data. The results revealed that the adsorption data fit better with the second-order kinetic model. Furthermore, the Freundlich model was found to be more suitable for describing the process of the separation of the dyes onto Fe3O4 (np)@CSs which were prepared at 250 °C and 400 °C, suggesting heterogenous surfaces and multi-layer adsorption.

The supercapattery designed with a binary composite of niobium silver sulfide (NbAg2S) and activated carbon for enhanced electrochemical performance.

A supercapattery is a hybrid device that is a combination of a battery and a capacitor. Niobium sulfide (NbS), silver sulfide (Ag2S), and niobium silver sulfide (NbAg2S) were synthesized by a simple hydrothermal method. NbAg2S (50/50 wt% ratio) had a specific capacity of 654 C g-1, which was higher than the combined specific capacities of NbS (440 C g-1) and Ag2S (232 C g-1), as determined by the electrochemical investigation of a three-cell assembly. Activated carbon and NbAg2S were combined to develop the asymmetric device (NbAg2S//AC). A maximum specific capacity of 142 C g-1 was delivered by the supercapattery (NbAg2S//AC). The supercapattery (NbAg2S/AC) provided 43.06 W h kg-1 energy density while retaining 750 W kg-1 power density. The stability of the NbAg2S//AC device was evaluated by subjecting it to 5000 cycles. After 5000 cycles, the (NbAg2S/AC) device still had 93% of its initial capacity. This research indicates that merging NbS and Ag2S (50/50 wt% ratio) may be the best choice for future energy storage technologies.

Facile Strategy for Fabricating an Organosilica-Modified Fe3O4 (OS/Fe3O4) Hetero-nanocore and OS/Fe3O4@SiO2 Core-Shell Structure for Wastewater Treatment with Promising Recyclable Efficiency.

The development of a sustainable process for heavy metal ion remediation has become a point of interest in various fields of research, including wastewater treatment, industrial development, and health and environmental safety. In the present study, a promising sustainable adsorbent was fabricated through continuous controlled adsorption/desorption processes for heavy metal uptake. The fabrication strategy is based on a simple modification of Fe3O4 magnetic nanoparticles with organosilica in a one-pot solvothermal process, carried out in order to insert the organosilica moieties into the Fe3O4 nanocore during their formation. The developed organosilica-modified Fe3O4 hetero-nanocores had hydrophilic citrate moieties, together with hydrophobic organosilica ones, on their surfaces, which facilitated the further surface coating procedures. To prevent the formed nanoparticles from leaching into the acidic medium, a dense silica layer was coated on the fabricated organosilica/Fe3O4 (OS/Fe3O4). In addition, the prepared OS/Fe3O4@SiO2 was utilized for the adsorption of cobalt(II), lead(II), and manganese(II) from the solutions. The data for the adsorption processes of cobalt(II), lead(II), and manganese(II) on OS/(Fe3O4)@SiO2 were found to follow the pseudo-second-order kinetic model, indicating the fast uptake of heavy metals. The Freundlich isotherm was found to be more suitable for describing the uptake of heavy metals by OS/Fe3O4@SiO2 nanoparticles. The negative values of the ΔG° showed a spontaneous adsorption process of a physical nature. The super-regeneration and recycling capacities of the OS/Fe3O4@SiO2 were achieved, comparing the results to those of previous adsorbents, with a recyclable efficiency of 91% up to the seventh cycle, which is promising for environmental sustainability.

Synthesis, characterization and adsorption behavior of modified cellulose nanocrystals towards different cationic dyes.

Green and efficient removal of polluted materials are essential for the sustainability of a clean and green environment. Nanomaterials, particularly cellulose nanocrystals (CNCs), are abundant in nature and can be extracted from various sources, including cotton, rice, wheat, and plants. CNCs are renewable biomass materials with a high concentration of polar functional groups. This study used succinic anhydride to modify the surface of native cellulose nanocrystals (NCNCs). Succinic anhydride has been frequently used in adhesives and sealant chemicals for a long time, and here, it is evaluated for dye removal performance. The morphology and modification of CNCs studied using FTIR, TGA & DTG, XRD, SEM, AFM, and TEM. The ability of modified cellulose nanocrystals (MCNCs) to adsorb cationic golden yellow dye and methylene blue dye was investigated. The MCNCs exhibited high adsorption affinity for the two different cationic dyes. The maximum adsorption efficiency of NCNCs and MCNCs towards the cationic dye was 0.009 and 0.156 wt%. The investigation for adhesive properties is based on the strength and toughness of MCNCs. MCNCs demonstrated improved tensile strength (2350 MPa) and modulus (13.9 MPa) using E-51 epoxy system and a curing agent compared to 3 wt% composites. This research lays the groundwork for environmentally friendly fabrication and consumption in the industrial sector.