Graphene Oxide Research Articles

Immobilization of Phospholipase D on Magnetic Graphene Oxide for Efficient Phosphatidylserine Production

Phosphatidylserine (PS) has significant applications in various sectors, such as the medical and food industries. However, its production relies heavily on phospholipase D (PLD), a crucial tool that is hindered by issues like poor stability and irrecoverability. Immobilization presents itself as an effective solution to overcome these limitations. In this study, magnetic graphene oxide (MGO) modified with an amino (NH2) group was synthesized and utilized for PLD immobilization. The activity of the immobilized PLD (MGO-PLD) reached 3062 U/gMGO, with a specific activity of 33.9 U/mgPLD, virtually identical to that of the free PLD. MGO-PLD was utilized to synthesize PS efficiently in a biphasic system. Under optimal conditions, the PS yield reached 18.66 g/L, with a conversion rate of 92.8% and a productivity of 3.11 g/L/h. Notably, MGO-PLD retained an impressive PS conversion rate of 77.4% even after seven repetitive usages. Moreover, MGO-PLD displayed enhanced thermal and pH resistance properties compared to free PLD, alongside augmented storage stability. After an 8-week preservation at 4 °C, its residual activity was maintained at 76.3%. This study provides a sustainable and highly efficient pathway for the biocatalytic synthesis of PS.

Zinc cobalt sulfide with carbon (graphene oxide and CNT) based nanocomposite as positive electrode for asymmetric coin cell supercapacitors

Abstract The world dependence on portable electronic devices has increased the demand for high-performance energy storage devices. The use of transition metal sulfides as faradaic electrode materials for electrochemical energy storage is rapidly increasing due to their high energy density. Herein Zinc Cobalt Sulfide (ZCS) with graphene oxide (GO) and carbon nanotubes (CNT) were used to create an interconnected ZCS composite network using a solvothermal technique. The materials were characterized by utilizing XRD, FT-Raman, TGA, FESEM/EDX, XPS, and BET. The electrochemical performance of the materials was examined using cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), and electrochemical impedance spectroscopy (EIS). The prepared electrodes exhibited both pseudocapacitor behavior and double-layer capacitor behavior, indicating the hybrid nature. Furthermore, All the electrode ZCS, ZCS/GO, ZCS/CNT, and ZCS/GO/CNT electrodes demonstrated higher capacitance behavior, with values of 420, 551, 585 and 811 F g−1 at 1 A/g. Among these ZCS/GO/CNT electrode exhibits outstanding electrochemical properties, with a notable retention of 81.08% at 10 Ag−1 because Combining ZCS nanoparticles with interconnected GO and CNT provides excellent electronic conductivity and stability. The assembled ZCS/GO/CNT//graphene oxide asymmetric coin cell (ACC) supercapacitor showed a high energy density of 33.3 Wh kg–1 at a power density of 624 W kg–1. The 3D nanostructure of ZCS/GO/CNT/Graphene oxide has great potential for developing foldable energy storage devices.

Synthesis and Characterization of New Chiral Polyurea‐Polyurethane Nanocomposites Incorporating Cinchona‐Derived Urea Organocatalysts

AbstractThe field of asymmetric organocatalysis has witnessed significant advancements in recent years, with chiral urea and thioureas emerging as powerful catalysts. In this study, we aimed to design novel polyurea‐polyurethane nanocomposites functionalized with cinchona urea groups, incorporating organoclay and graphene oxide, to serve as heterogeneous organocatalysts in asymmetric synthesis. The synthesis of these polyurea‐polyurethane nanocomposites was achieved through a two‐component polycondensation reaction. The resulting chiral polyurea‐polyurethanes (PU‐PURs) exhibited favorable yields and demonstrated precise control over stereochemistry, resulting in high enantioselectivity. The incorporation of nanocomposites, such as CU‐MMT and graphene oxide (GO), significantly enhanced the catalytic performance of the PU‐PURs. The CU‐MMT nanocomposites exhibited higher catalytic activity, while the PU‐PURs/GO still exhibited enantioselectivity greater than 99 %. Overall, this study highlights the potential of these novel polyurea‐polyurethane nanocomposites as efficient and versatile heterogeneous organocatalysts in asymmetric synthesis.

A BIONIC-INSPIRED DRAGONFLY ALGORITHM FOR PARAMETRIC OPTIMIZATION AND DAMAGE INVESTIGATION DURING MACHINING OF MODIFIED POLYMER NANOCOMPOSITE

Polymer nanocomposite is commonly used to develop structural components of space, aircraft, biomedical, sensor, automobile, and battery sector applications. It remarkably substitutes the heavyweight metallic and nonmetallic engineering materials. The machining principles of polymer nanocomposites are intensely different and complex from traditional metals and alloys. The nonhomogeneity, abrasive, and anisotropic nature differs its machining aspect from conventional metallic materials. This investigation aims to execute the CNC drilling of modified nanocomposite using Graphene–carbon (G-C) @ epoxy matrix. The process constraints, namely, cutting speed (S), feed (F), and wt.% of graphene oxide (GO) vary up to three levels and are designed according to the response surface methodology (RSM) array. The nonlinear model is created to predict surface roughness (Ra) and delamination (Fd) on regression analysis. It has been found that the average error for Ra is 0.94% and for Fd it is 3.27%, which is acceptable in model predictions. The metaheuristics-based evolutionary Dragonfly algorithm (DA) evaluated the optimal parametric condition. The optimal setting prediction for the DA is observed as cutting speed (S)-37.68[Formula: see text]m/min, feed (F)-80[Formula: see text]mm/min, and wt.% of graphene oxide (GO)-1%. This algorithm demonstrates a higher application potential than the previous efforts in controlling Ra and Fd values. Both the drilling response values are found to be minimized when the cutting speed increases and the feed decreases. The best fitness value for the DA is 1.626 for surface roughness and 5.086 for delamination. This study agreed with the prediction model’s outcomes and the process parameters’ optimal condition. The defects generated during the sample drilling, such as fiber pull out, uncut/burr, and fiber breakage, were examined using FE-SEM analysis. The optimal findings of the DA module significantly controlled the damages during machining.

Experimental Investigation οf Bio-Based Polymers Reinforced with Graphene Oxide

Experimental Investigation οf Bio-Based Polymers Reinforced with Graphene Oxide

Microwave‐assisted control of PtNi nanoalloy clusters on the nitrogen‐doped graphene oxide for energy conversion with oxygen reduction reaction and hydrogen evolution reaction

AbstractResearch on the production and utilization of hydrogen energy is essential to overcome the environmental issues caused by fossil fuels. Herein, we anchor PtNi nanoalloy clusters (Pt‐Ni NACs) on nitrogen‐doped graphene oxide (NrGO) by a facile microwave‐assisted synthesis and analyze the variations of catalyst properties based on the PtNi composition and the presence of nitrogen. Ni inclusion in the Pt matrix can induce lattice strain and change the electronic structure, while the doped nitrogen into the graphene can enhance electron transfer and improve the durability of the catalyst through strong chemical bonding with the alloy clusters. TEM analysis discovers that the NACs are uniformly decorated in a few‐nanometer‐size on the graphene surface, and the formation of the PtNi NACs and structural changes according to composition are confirmed through XRD and XPS. In addition, the structural changes due to N‐doping and its bonding with the NACs are observed through Raman spectroscopy and XPS. Electrochemical measurements reveal that Pt2.6Ni NACs/NrGO exhibits the highest ORR onset potential (0.893 V) and the lowest HER overpotential at 10 mA cm−2 (22 mV) among other catalysts, and those activities are almost unchanged under long‐term durability tests. From these results, Pt2.6Ni NACs/NrGO is utilized in a zinc‐air battery (ZAB) system, demonstrating better battery performance than commercial Pt and Ir‐based catalysts. Moreover, it is applied to hydrogen collection, showing linear trend in hydrogen production over time, confirming the catalyst's availability in hydrogen production and utilization.image

Chitosan/Nitrogen-doped graphene nanocomposite for supercapacitor application

Abstract In this study, we explore the chitosan/nitrogen-doped graphene oxide (CS-NGO) nanocomposite using the hydrothermal method and incorporate it onto carbon paper by a deep coating technique for supercapacitor applications. The incorporation of CS-NGO, a non-toxic and environmentally friendly material, significantly enhances the electrochemical performance. The electrochemical properties are explored by cyclic voltammetry (CV), galvanostatic charge-discharge (GCD), and impedance spectrum (EIS). The analyses reveal a specific capacitance increase from 2.84 μF cm−2 to 3.96 μF cm−2, a reduction in charge transfer resistance (Rct) from 24.75 Ω to 16.74 Ω, a decrease in Rs resistance from 4.9 Ω to 0 Ω, and a reduction of equivalent series resistance (ESR) from 12.87 Ω to 6.41 Ω. In addition, the results demonstrate remarkable enhancements in energy density and power density and an excellent cyclic stability of 100% over up to 1000 CV cycles of the CS-NGO electrode. These improvements are due to the potential of CS-NGO nanocomposite in developing high-performance, sustainable supercapacitors with the growing demand for green and safe energy storage solutions. This sign of success in this research is due to the new nanocomposite.

Cotton fabric coated with graphene oxide nanosheets and CuO nanoparticles as a “dip catalyst” for the photocatalytic degradation of dyes

This research focuses on the immobilization in-situ of CuO nanoparticles on graphene oxide nanosheets modified cotton fabric (CuO/GO@CF) for the photodegradation, of organic dyes. The process involves coating the fabrics (CF) with graphene oxide (GO) nanosheets through sonication.The produced CuO, GO@CF, and CuO/GO@CF have been characterized utilizing various physicochemical methods, such as X-ray diffraction (XRD), Fourrier Transformed Infra-Red (FTIR), trans mission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and Thermogravimetric analysis (TGA).The catalytic activity of the nanocomposite was assessed by methylene blue (MB) oxidation. Additionally, a detailed analysis was conducted to determine how various parameters, including catalyst surface, pH, MB concentration and CuO loading (%), affected the degradation efficiency. The results showed that the 10 %CuO/5 %GO@CF with a surface of 4 cm2 (2 × 2 cm) exhibited the highest catalytic activity, achieving a MB removal efficiency of 82 % in 90 min. Additionally, after successive reaction cycles, the synthesized composite showed excellent stability and no appreciable drop-in catalytic activity. Moreover, it was shown that the primary reactive oxidative species (ROSs) in charge of the extremely effective MB breakdown were HO.. Lastly, catalyst stability and recyclability showed that CuO/GO@CF might be used as a substitute photocatalyst for environmental cleanup and dye degradation. This synthetized composite can be easily added to and removed from the reaction solution while maintaining high catalytic performance in the removal of dyes and it could be beneficial in avoiding problems related to powder separation.

Unlocking Superior Hydrogen Oxidation and CO Poisoning Resistance on Pt Enabled by Tungsten Nitride-Mediated Electronic Modulation.

Enhancing the activity and CO poisoning resistance of Pt-based catalysts for the anodic hydrogen oxidation reaction (HOR) poses a significant challenge in the development of proton exchange membrane fuel cells. Herein, we leverage theoretical calculations to demonstrate that tungsten nitride (WN) can intricately modulate the electronic structure of Pt. This modulation optimizes the hydrogen adsorption, significantly boosting HOR activity, and simultaneously weakens the CO adsorption, markedly improving resistance to CO poisoning. Through prescreening with rational design, we synthesized an efficient catalyst comprising a minimal Pt content (only 1.4 wt %) supported on the small-sized WN/reduced graphite oxide (Pt@WN/rGO). As anticipated, this catalyst showcases a remarkable acidic HOR mass activity of 3060 A gPt-1, which is approximately 11.8 times greater than that of the commercial 20 wt % Pt/C catalyst. Impressively, it maintains high activity with 98.2% retention even in the presence of 1000 ppm of CO, indicating exceptional poison resistance. Operando synchrotron radiation analyses reveal that WN harmonizes the electron state of Pt during electrochemical reactions, optimizing hydrogen adsorption/desorption dynamics. This leads to a lower peak potential of CO stripping on Pt@WN/rGO compared to that on Pt/rGO, suggesting that WN mitigates competitive CO adsorption and enhances the availability of hydrogen adsorption sites on Pt. The synergistic effect significantly accelerates HOR activity and increases antipoisoning efficacy. The assembled PEMFC demonstrates substantial tolerance to CO concentration from 10 to 1000 ppm in the H2/CO mixture.

Reduced Graphene Oxide-Substituted Nanohydroxyapatite: Rejuvenating Bone-Nerve Crosstalk with Electrical Cues in a Fragility Fracture Rat Model under Hyperglycemia.

Diabetes has currently acquired the status of epidemic worldwide, and among its various pathological consequences like retinopathy and nephropathy, bone fragility fractures from diabetic osteopathy occurs in later stages and is equally destructive. Chronic hyperglycemia culminates into deteriorating microvasculature and quality of bone, making it prone to fractures. Among these, hip fractures are most common, especially in older diabetic patients apart from underlying neuropathy. Our study is an attempt to ameliorate hip fragility fracture and nerve trauma with electrical stimulation as an interface in a chronic diabetic rat model. We have fabricated reduced graphene oxide-substituted hydroxyapatite as an electroactive bone substitute and incorporated it into chitosan gelatin cryogels. The in situ reduction of graphene oxide during sintering of hydroxyapatite imparts higher potential to the fabricated composite in dealing with problem at question. The cryogels depicted optimum in vitro biocompatibility and enhanced mineralization after ectopic subcutaneous implantation in rats. The therapeutic potency of composite cryogels was evaluated in a hip fracture model with compression to the sciatic nerve in diabetic rats, mimicking the severe clinical trauma. The presence of cryogels in the femoral neck canal coupled with electrical stimulation and biochemical factors significantly improved bone regeneration in diabetic rats as depicted with microcomputed tomography analysis and histology images. The application of electrical stimulation also ameliorated the nerve trauma observed with 70% improvement in electrophysiological parameters such as the compound muscle action potential with combinatorial therapy. We therefore report the successful implication of a multitarget therapy in a chronic diabetic rat model unraveling the bone-nerve crosstalk with electroactive smart cryogels.

Fully Stretchable Microbial Fuel Cell with 75% Stretchability.

A decent stretchability is of paramount significance to operate microbial fuel cell (MFC) under mechanically dynamic conditions. However, it remains a grand challenge to fabricate fully stretchable MFC without compromising its power output. Here, using Shewanella oneidensis MR-1 (S. oneidensis) as the model electrogenic bacteria, the study demonstrates a fully stretchable MFC device that can operate with a stretchability of 75%. The design takes advantage of a stretchable and ion-conductive polyurethane membrane, which encapsulates the biohybrids composed of S. oneidensis and reduced graphene oxide (rGO) on the polydimethylsiloxane (PDMS) current collector for synchronous stretching. It is discovered that the "stretchable" living biohybrids can sustain an adaptive bio-current output under stretching/releasing stimulation. The design also employs a stretchable air cathode. The stabilized peak power density of the stretchable MFC follows an increasing trend with the applied strain, and reaches 5.0±0.7, 5.9±0.9, 6.2±1.1, 6.6±1.4µW cm-2 at strains of 0%, 25%, 50%, and 75%, respectively (n = 3). At 75% strain, the stretchable MFC yields a maximum current output of 104±27 µA cm-2 and an open-circuit voltage of 283±30mV (n = 3). The results provide insights to design stretchable MFCs to power the next-generation on-skin devices, soft robotics, and sustainable electronics.

Bifunctional SnO2/NiO/rGO nanocomposite electrode for hydrogen evolution reaction and detection of winter wheat cold-resistant RNA.

Aconvenient, non-toxic, and low-cost tin dioxide (SnO2)/nickel oxide (NiO)/reduced graphene oxide (rGO) nanocatalytic electrode was investigated, which can effectively promote the hydrogen evolution reaction and can also be used to construct a sensitive winter wheat cold-tolerant RNA sensor. Due to the good synergy and photocurrent generation between SnO2 and NiO, which accelerates the electron transfer and catalyzes the hydrolysis reaction, the resultant data for the hydrogen evolution reaction in alkaline environment of this material are very impressive, with cathodic current densities of up to 10mAcm-2. The marvelous heterostructures and photovoltaic properties form a signal amplification system, which enables the nanocomposites to have an excellent linear sensitivity in low-concentration RNA solutions. The single-stranded complementary RNA of the target RNA was immobilized on the surface of the nanocomposites, which enabled the materials to recognize the target RNA under enzyme-free conditions. The test results showed that the modified electrode materials had good single detection performance in a wide linear range from 0.1nM to 2mM, with the limit of detection (LOD) of 0.078nM. The developed nanocomposite electrode has good performance in hydrogen evolution and winter wheat cold-resistant RNA detection, and is a bifunctional device with superior performance.

Inclusion of Reduced Graphene Oxide to Silk Fibroin Hydrogels Improve the Conductive, Swelling and Wound Healing Capacity

AbstractDeveloping dressing for wound dressings represents a significant challenge for the scientific community. In this study, a conductive hydrogel was synthesized to promote the wound‐healing process. This hydrogel is composed of silk fibroin (SF), reduced graphene oxide (rGO), and glycerol (G). The impact of modifying the SF:rGO ratio, and the G content (%), on the physicochemical and biological properties. The hydrogels were characterized using FT‐IR, SEM, XRD, TGA, swelling, mechanical resistance, and conductivity. The cytotoxicity of the materials and their wound‐healing capacity in human fibroblasts were also determined. Chemical analysis revealed that the gelation of SF occurs due to the formation of β sheet structures, which was confirmed by the shift from amide I to amide II. An Increase in the SF:rGO ratio favored swelling behavior, although increasing G reduced this effect. The swelling of the hydrogel followed a Fick diffusion mechanism. Furthermore, the increase in the SF:rGO ratio and the percentage G improved the conductivity of the materials. The hydrogels were found to be non‐cytotoxic to human fibroblasts, and those containing rGO exhibited superior wound healing capacity compared to the positive control cell culture medium. Therefore, SF:rGO hydrogels could be considered promising candidates for wound dressing.

Hierarchically Structured Conductive Lanthanide Metal Organic Framework Nanorods for Ultrastable Flexible Magnesium Ion Capacitors

AbstractAqueous multivalent metal ion capacitors are very attractive owing to their high capacitance, low cost, environmental benignity, and safety. Herein, hierarchically structured, conductive lanthanide metal‐organic frameworks (MOFs) assembled by nanorods for ultrastable flexible magnesium ion capacitors (MICs) is designed. Three MOFs, consisting of lanthanide metals (La, Ho, and Yb) and 2,3,6,7,10,11‐hexahydroxytriphenylene (HHTP), are structurally stabilized through the covalent bonds and electronically conductive due to π‐d conjugation. Among 3 MOFs, Ho‐HHTP electrodes in a full‐cell system achieved long‐term cyclic stability with a high capacitance retention of 65.0% after 12 000 cycles and a high Coulombic efficiency of 96.9%. Furthermore, flexible pouch cells are fabricated using Ho‐HHTP as anode, reduced graphene oxide as cathode, and poly(vinyl alcohol) (PVA)/Mg(ClO4)2 as gel electrolyte, demonstrating a low capacitance decay rate of 0.00444% per cycle during 10 000 cycles owing to the hierarchical structure and intrinsic electronic conductivity. As indicated by density functional theory and spectroscopic characterizations, Mg2+ ions are faradaically stored in the catechol part of the ligand, and Mg2+ inserted into the vacant Ho sites contributes to structural stability. Furthermore, operando 2D correlation Raman spectroscopy identified how Mg2+ ions interact with the ligand of Ho‐HHTP and demonstrated the sequential change of peak change.

Enhanced antibiotic degradation using rGO composites under visible light photocatalysis

A robust reduced graphene oxide (rGO), polyaniline (PANI) with calcium (Ca) and magnesium (Mg) bimetallic nanocomposite was successfully prepared using an in-situ chemical facial reducing method and named rGO@PANI-Ca:Mg. Various spectroscopic techniques, including XRD, SEM, TEM, XPS, and supplementary methods, were utilized to characterize the catalyst phase, microstructure, and optical attributes. The composite's photocatalytic efficiency was assessed by degrading antibiotics such as ciprofloxacin (CP) and tetracycline (TC) using calcium peroxide (CaO2) under visible light irradiation. The rGO@PANI-Ca:Mg composite demonstrates superior degradation efficiency for CP, 45 %, and for TC, 70 %, achieving a correlation coefficient R² of 0.94 and 0.991 respectively. This performance surpasses that of pristine GO, rGO, and rGO@PANI. The heightened photocatalytic activity is ascribed to forming a heterojunction, effectively mitigating electron-hole pair recombination. The incorporation of CaO2 promotes the generation of additional active reactive oxygen species (ROS), particularly OH·, ·O2−, e-, h+, as verified by radical scavenging experiments, indicating an enhancement in the degradation and a potential mechanism is also suggested. The degradation rate of TC, CP, and real wastewater (RW) is about 71 %, 45 %, and 40.98 %, respectively. The composite demonstrates stability and reusability for up to three catalytic cycles. Our experiments also showed that when bacteria were treated with a 2 mg catalyst, the minimum inhibitory concentration (MIC) was determined to be at a 10−3 dilution. This MIC value represents the lowest concentration at which the catalyst effectively inhibited bacterial growth, as evidenced by clear inhibition zones.

Flexible Supercapacitor Device Based on Laser‐Synthesized Nanographene for Low‐Power Applications

Laser‐induced graphene (LIG) and laser‐induced reduced graphene oxide (LIrGO) are two relatively recent graphene‐based nanoscale materials suitable for miniaturized flexible supercapacitors. This study employs direct laser engraving techniques to generate patterns on flexible substrates, such as paper and polyamide (PI). This methodology allows fine control over the formed nanographene structures to fabricated LIG and LIrGO supercapacitors. The LIG on PI exhibits a distinctive porous structure and high surface area, adsorption, and transportation of ions. Furthermore, paper‐based LIrGO electrodes are recyclable and are formed in a single step. The morphological study is done using scanning electron microscopy, Raman spectroscopy, X‐ray photoelectron spectroscopy, and X‐ray diffraction. Galvanostatic charge–discharge studies at 0.05 mA cm−2 current density show an areal capacitance of 3.69 mF cm−2 for LIG and 1.61 mF cm−2 for LIrGO. The comparable energy densities for LIG and LIrGO are 0.32 and 0.16 μWh cm−2, respectively. From the calculative analysis of both types, the variation in specific areal capacitance enabling effective is 56.3% from GCD, indicating that the LIG device performs better. Finally, a portable potentiostat is employed to investigate the viability of utilizing supercapacitors to operate self‐powered sensors in a portable and integrable fashion.

Novel synthesis of CuHCF/B-rGO composites for oxygen evolution reaction activity

In this work, we have focused on the preparation of copper hexacyanoferrate/boron doped rGO composites (abbreviated as CuHCF/B-rGO) by employing simple co-precipitation technique subsequently processed with ultrasonication method. The XRD spectra confirmed the existence of the cubic structure of copper hexacyanoferrate with high crystalline peaks. The prepared nanocomposite morphology was evaluated by scanning electron microscopy (SEM), and confirmed CuHCF nanoparticles formation with flake-like and wrinkled sheets. Pure CuHCF nanostructures revealed good OER action at 430 mV to obtain 10 mA/cm2. The obtained CuHCF product OER activity can be further upgraded by incorporating the electrically conductive boron doped reduced graphene oxide matrix into CuHCF nanostructures, for the reason that the overpotential of the CuHCF/B-rGO was reduced to 380 mV to attain 10 mA/cm2 with 88 mV/dec Tafel slope value. The doping of heteroatom considerably improves charge-transfer resistance of metal hexacyanoferrate, giving a small resistance value of 2.97 Ω, which was lower than that of CuHCF (5.57 Ω) and CuHCF/rGO (4.31 Ω). Furthermore, the catalytic activity of the CuHCF/B-rGO was stable at prolonged hours with a small decay of 12.5%. Therefore, this work offers new approach to stimulate the catalytic performance of metal hexcyanoferrate by highly conductive carbon-based materials for water splitting performance.

Graphene Oxide and its Composites: Advanced Membranes for Selective Water Permeation.

Graphene oxide (GO) membranes have gained significant attention as a promising material for separation by selective permeation processes due to their advantageous structural and chemical properties, including high water permeability, chemical resistance, and mechanical strength. In this study, we explore the potential applications of GO membranes in pervaporation to separate liquid mixtures. The layered structure and hydrophilic nature of GO membrane facilitate rapid and selective water transport through angstrom-scale interlayer spacings, resulting in superior performance over conventional polymeric and inorganic membranes. The unique mass transport mechanisms - slip flow and molecular alignment - enable GO membranes to selectively permeate water over organic solvents. For chemical dehydration, GO membranes are the most potential candidates. Furthermore, advancements in composite GO membranes and cross-linking techniques that improve their stability and separation performance are discussed. This study highlights the advantages of GO membranes and their potential to replace or complement existing technologies, by emphasizing their role in advancing membrane-based separation and promoting environmental sustainability. Future research is expected to optimize the fabrication techniques for GO membranes and expand their application scope.

Adsorptive Removal of Dyes: A Comparison of Graphene Oxide to Granular Activated Carbon and Zeolite NaY

Synthetic carbon-based compounds are a prevalent wastewater contaminant that can adversely impact water resources due to their potential carcinogenic and toxic effects on aquatic biota and human health. This research investigates the versatility of graphene oxide (GO) as an alternative to commonly used adsorbents (zeolite NaY (NaY) and granular activated carbon (GAC)) for removal of synthetic cationic dyes. Rhodamine B (RhB) and methylene blue (MB), were selected as the target contaminants to represent cationic synthetic dyes with differing molecular sizes and structural compositions. Batch experiments using GO, NaY, and GAC as adsorbents were used to assess both physicochemical interactions between adsorbent surfaces and contaminants, and removal efficiency. GO demonstrated the highest removal efficiency for both target contaminants—at 99% and 86%, respectively—while the lowest removal efficiency was observed for NaY. Langmuir, Freundlich, Temkin, and BET isotherm models were used to describe the adsorption isotherms. Overall, GO demonstrated a more robust and higher removal efficiency of cationic dyes compared with GAC and NaY, indicating the potential of graphene oxide for the removal of complex structured organic contaminants in wastewater treatment.

Cytotoxicity and photothermal properties of graphene oxide conjugate with folic acid and a cytostatic agent of styryl thiazolopyrimidinium class

ABSTRAСT In recent years, the field of nanomedicine has garnered significant attention, particularly in the development of advanced drug delivery systems. Among the promising materials, highly oxidized graphene oxide (GO) has emerged as key components due to unique physicochemical properties and biocompatibility. These materials offer novel avenues for targeted drug delivery, enhancing therapeutic efficacy while minimizing side effects. This article explores the innovative design of nanoparticle-based drug delivery systems utilizing highly oxidized graphene oxide with folic acid in combination with thiazolopyrimidinium salt, highlighting their potential applications in medicine.