Potential Of Graphene Oxide Research Articles

Novel Structures of Functionalized Graphene Oxide with Hydrazide: Characterization and Bioevaluation of Antimicrobial and Cytocompatibility Features

Graphite was oxidized to graphene oxide and activated by thionyl chloride, for further covalently linking three hydrazides with potential biological activity. The obtained materials were characterized by scanning electron microscopy with energy dispersive spectroscopy, Fourier-transform infrared and Raman spectroscopies. The presence of various functional groups specific to graphene oxide (GO) functionalized with different hydrazides was confirmed by spectral data. The ratio between D- and G-bands, observed in Raman spectra, allowed for an evaluation of the disorder degree and the mean crystallite size of the samples. The micrographs highlighted that the samples lead to the occurrence of disorders, probably caused by the sp3 carbons, the formation of oxygen-containing functional groups in the basal planes, and by various structural defects. The new graphene oxide–hydrazide derivatives were tested for their antimicrobial and cytotoxicity activity. Their antimicrobial activity against planktonic and biofilm-embedded cells was inferior to that of free hydrazides, except for GO-3 against planktonic Escherichia coli and GO-2 against Pseudomonas aeruginosa biofilm, demonstrating that further optimization is needed to be able to exploit the huge potential of GO for developing potent antimicrobials.

Bioactivity of PEGylated Graphene Oxide Nanoparticles Combined with Near-Infrared Laser Irradiation Studied in Colorectal Carcinoma Cells.

Central focus in modern anticancer nanosystems is given to certain types of nanomaterials such as graphene oxide (GO). Its functionalization with polyethylene glycol (PEG) demonstrates high delivery efficiency and controllable release of proteins, bioimaging agents, chemotherapeutics and anticancer drugs. GO–PEG has a good biological safety profile, exhibits high NIR absorbance and capacity in photothermal treatment. To investigate the bioactivity of PEGylated GO NPs in combination with NIR irradiation on colorectal cancer cells we conducted experiments that aim to reveal the molecular mechanisms of action of this nanocarrier, combined with near-infrared light (NIR) on the high invasive Colon26 and the low invasive HT29 colon cancer cell lines. During reaching cancer cells the phototoxicity of GO–PEG is modulated by NIR laser irradiation. We observed that PEGylation of GO nanoparticles has well-pronounced biocompatibility toward colorectal carcinoma cells, besides their different malignant potential and treatment times. This biocompatibility is potentiated when GO–PEG treatment is combined with NIR irradiation, especially for cells cultured and treated for 24 h. The tested bioactivity of GO–PEG in combination with NIR irradiation induced little to no damages in DNA and did not influence the mitochondrial activity. Our findings demonstrate the potential of GO–PEG-based photoactivity as a nanosystem for colorectal cancer treatment.

Extraordinary Protective Efficacy of Graphene Oxide over the Stone‐Based Cultural Heritage

AbstractThe deterioration of monumental stones is a common event occurring to our historical and cultural heritage, threatening the preservation of our social identity and its legacy to future generations. The prolonged effect of inclement weather is very harmful for particular stone materials such as limestone and dolomite, to which a truly effective and durable protective agent has not yet been found. Herein, an unprecedented performance of graphene oxide (GO) for the shielding of carbonated ornamental stones against environmental aggressions, namely intense rainfall and extreme temperatures, is demonstrated. A simple additive‐free aqueous suspension of GO serves as the perfect coating, exceedingly preventing from any kind of wear or erosion after different climatic simulations. Additionally, the stones’ original aesthetics is not altered (a critical issue in monuments), together with an improvement in their mechanical properties, reasserting the unique potential of GO for conserving exposed stone‐based monuments in an affordable, accessible, and revolutionary way.

Synergistic Antifungal Activity of Graphene Oxide and Fungicides against Fusarium Head Blight In Vitro and In Vivo.

Plant pathogens constantly develop resistance to antimicrobial agents, and this poses great challenges to plant protection. Therefore, there is a pressing need to search for new antimicrobials. The combined use of antimicrobial agents with different antifungal mechanisms has been recognized as a promising approach to manage plant diseases. Graphene oxide (GO) is a newly emerging and highly promising antimicrobial agent against various plant pathogens in agricultural science. In this study, the inhibitory activity of GO combined with fungicides (Mancozeb, Cyproconazol and Difenoconazole) against Fusarium graminearum was investigated in vivo and in vitro. The results revealed that the combination of GO and fungicides has significant synergistic inhibitory effects on the mycelial growth, mycelial biomass and spore germination of F. graminearum relative to single fungicides. The magnitude of synergy was found to depend on the ratio of GO and fungicide in the composite. In field tests, GO–fungicides could significantly reduce the disease incidence and disease severity, exhibiting a significantly improved control efficacy on F. graminearum. The strong synergistic activity of GO with existing fungicides demonstrates the great application potential of GO in pest management.

Histological and Histochemical Evaluation of the Effects of Graphene Oxide on Thyroid Follicles and Gas Gland of Japanese Medaka (Oryzias latipes) Larvae

Graphene oxide (GO) has become a topic of increasing concern for its environmental and health risks. However, studies on the potential toxic effects of GO, especially as an endocrine disrupting chemical (EDC), are very limited. In the present study we have used Japanese medaka fish as a model to assess the endocrine disruption potential of GO by evaluating its toxic and histopathologic effects on thyroid follicles and the gas gland (GG) of medaka larvae. One day post-hatch (dph) starved medaka fries were exposed to GO (2.5, 5.0, 10.0, and 20 mg/L) for 96 h, followed by 6 weeks depuration in a GO-free environment with feeding. Larvae were sacrificed and histopathological evaluation of thyroid follicles and the GG cells were done microscopically. Different sizes of spherical/oval shape thyroid follicles containing PAS positive colloids, surrounded by single-layered squamous/cuboidal epithelium, were found to be scattered predominantly throughout the pharyngeal region near the ventral aorta. We have apparently observed a sex-specific difference in the follicular size and thyrocytes height and a non-linear effect of GO exposure on the larvae on 47th day post hatch (dph). The GG is composed of large uniform epithelial cells with eosinophilic cytoplasm. Like thyroids, our studies on GG cells indicate a sex-specific difference and GO exposure non-linearly reduced the GG cell numbers in males and females as well as in XY and XX genotypes. Our data further confirm that sex effect should be carefully considered while assessing the toxicity of EDCs on the thyroid gland.

Graphene oxide based electrochemical immunosensor for rapid detection of groundnut bud necrosis orthotospovirus in agricultural crops

Groundnut bud necrosis orthotospovirus (GBNV) is one of the causative plant viruses responsible for the outbreak of many viral epidemics in food crops across India and other south-Asian countries. Its management is a major challenge due to fast vector transmission, and the non-availability of appropriate agrochemical treatment. The timely detection of GBNV becomes indispensable for the effective management of viral infection and the periodic monitoring of plant health. We report the fabrication of graphene oxide (GO) based electrochemical immunosensor for the rapid and sensitive detection of GBNV. The immunoelectrode is prepared by depositing GO onto indium-tin oxide (ITO) coated glass substrates and functionalized by anti-GBNV antibodies using N-ethyl-N′-(3- dimethylaminopropyl) carbodiimide hydrochloride and N-hydroxysuccinimide (EDC-NHS) conjugation chemistry. The response measurements of the immunoelectrodes revealed a sensitivity of 221 ± 1 μA μg−1 mL−1(n = 3) and limit of detection (LOD) of 5.7 ± 0.7 ng mL−1(n = 3) for the standard concentrations of GBNV antigen. Further, the GBNV detection was carried out in infected leaf extracts of three different host plants i.e., Tomato, Cowpea, and N. benthamiana, and the results have been compared with the conventionally used direct antigen coated enzyme-linked immunosorbent assay (DAC-ELISA) technique. The comparable results obtained for the detection of GBNV in infected plants using electrochemical immunosensing and DAC-ELISA techniques advocated the immense potential of GO based immunosensor as a point-of-care sensing device that is poised to overcome the limitations of the traditional methods of virus detection in field conditions and may transform the diagnostics in agriculture.

Inhibition of microtubule assembly and cytotoxic effect of graphene oxide on human colorectal carcinoma cell HCT116

Nanomaterials, such as graphene oxide (GO), are increasingly being investigated for their suitability in biomedical applications. Tubulin is the key molecule for the formation of microtubules crucial for cellular function and proliferation, and as such an appealing target for developing anticancer drug. Here we employ biophysical techniques to study the effect of GO on tubulin structure and how the changes affect the tubulin/microtubule assembly. GO disrupts the structural integrity of the protein, with consequent retardation of tubulin polymerization. Investigating the anticancer potential of GO, we found that it is more toxic to human colon cancer cells (HCT116), as compared to human embryonic kidney epithelial cells (HEK293). Immunocytochemistry indicated the disruption of microtubule assembly in HCT116 cells. GO arrested cells in the S phase with increased accumulation in Sub-G1 population of cell cycle, inducing apoptosis by generating reactive oxygen species (ROS) in a dose- and time-dependent manner. GO inhibited microtubule formation by intervening into the polymerization of tubulin heterodimers both in vitro and ex vivo, resulting in growth arrest at the S phase and ROS induced apoptosis of HCT116 colorectal carcinoma cells. There was no significant harm to the HEK293 kidney epithelial cells used as control. Our report of pristine GO causing ROS-induced apoptosis of cancer cells and inhibition of tubulin-microtubule assembly can be of interest in cancer therapeutics and nanomedicine.

TGF-β3-loaded graphene oxide - self-assembling peptide hybrid hydrogels as functional 3D scaffolds for the regeneration of the nucleus pulposus

Intervertebral disc (IVD) degeneration is a process that starts in the central nucleus pulposus (NP) and leads to inflammation, extracellular matrix (ECM) degradation, and progressive loss of disc height. Early treatment of IVD degeneration is critical to the reduction of low back pain and related disability. As such, minimally invasive therapeutic approaches that can halt and reverse NP degeneration at the early stages of the disease are needed. Recently, we developed an injectable graphene oxide (GO) - self-assembling peptide FEFKFEFK (F: phenylalanine; K: lysine; E: glutamic acid) hybrid hydrogels as potential delivery platform for cells and/or drugs in the NP. In this current study, we explored the possibility of using the GO present in these hybrid hydrogels as a vehicle for the sequestration and controlled delivery of transforming growth factor beta-3 (TGF-β3), an anabolic growth factor (GF) known to direct NP cell fate and function. For this purpose, we first investigated the potential of GO to bind and sequestrate TGF-β3. We then cultured bovine NP cells in the new functional scaffolds and investigated their response to the presence of GO and TGF-β3. Our results clearly showed that GO flakes can sequestrate TGF-β3 through strong binding interactions resulting in a slow and prolonged release, with the GF remaining active even when bound to the GO flakes. The adsorption of the GF on the GO flakes to create TGF-β3-loaded GO flakes and their subsequent incorporation in the hydrogels through mixing, [(GO/TGF-β3Ads)-F8] hydrogel, led to the upregulation of NP-specific genes, accompanied by the production and deposition of an NP-like ECM, rich in aggrecan and collagen II. NP cells actively interacted with TGF-β3-loaded GO flakes and remodeled the scaffolds through endocytosis. This work highlights the potential of using GO as a nanocarrier for the design of functional hybrid peptide-based hydrogels. Statement of significanceIntervertebral disc (IVD) degeneration is a process that starts in the central nucleus pulposus (NP) and leads to inflammation, extracellular matrix (ECM) degradation, and progressive loss of disc height. As such, minimally invasive therapeutic approaches that can halt and reverse NP degeneration at the early stages of the disease are needed. In this current study, we explored the possibility of using peptide - GO hybrid hydrogels as a vehicle for the sequestration and controlled delivery of transforming growth factor beta-3 (TGF-β3), an anabolic growth factor (GF) known to direct NP cell fate and function.

Effect of root exudates on the stability and transport of graphene oxide in saturated porous media

Root exudates are a major source of dissolved organic matters that strongly affect the stability and transport behaviors of nanomaterials in porous media. This study investigated the effect of citric acid (CA) and oxalic acid (OA), two common low molecular weight root exudates, on the stability and transport of graphene oxide (GO) in saturated sand columns under different combinations of pH (4.5, 7.0), ionic strength (IS: 10, 50 mM), and organic acid concentrations (10, 25 mM). Both OA and CA accelerated GO aggregation, especially under high IS and acid concentration conditions. With the presence of OA/CA (≥ 10 mM), the transport of GO was higher at pH of 7.0 than 4.5, and the GO mobility decreased with increasing IS and OA/CA concentrations, whereas, enhanced GO transport was observed at a low concentration of OA/CA (0.1 mM), indicating that the influence of organic acid was concentration-dependent. All the results suggest that perturbations of surface potential of GO and sand, as well as the chemical structure of organic acids under different solution chemistry conditions are crucial in controlling GO stability and transport behaviors. Mathematical models based on the advection-dispersion equation with one-site kinetics simulated the experimental breakthrough curves of GO very well.

TGF-β3-Loaded Graphene Oxide - Self-Assembling Peptide Hybrid Hydrogels as Functional 3D Scaffolds for the Regeneration of the Nucleus Pulposus

Intervertebral disc (IVD) degeneration is a process that starts in the central nucleus pulposus (NP) and leads to inflammation, extracellular matrix (ECM) degradation, and progressive loss of disc height. Early treatment of IVD degeneration is critical to the reduction of low back pain and related disability. As such, minimally invasive therapeutic approaches that can halt and reverse NP degeneration at the early stages of the disease are needed. Recently, we developed novel injectable graphene oxide (GO) - self-assembling peptide FEFKFEFK (F: phenylalanine; K: lysine; E: glutamic acid) hybrid hydrogels as potential delivery platform for cells and/or drugs in the NP. In this current study, we explored the possibility of using the GO present in these hybrid hydrogels as a vehicle for the sequestration and controlled delivery of transforming growth factor beta-3 (TGF-β3), an anabolic growth factor (GF) known to direct NP cell fate and function. For this purpose, we first investigated the potential of GO to bind and sequestrate TGF-β3. We then cultured bovine NP cells in the new functional scaffolds and investigated their response to the presence of GO and TGF-β3. Our results clearly showed that GO flakes can sequestrate TGF-β3 through strong binding interactions resulting in a slow and prolonged release with the GF remaining active even when bound to the GO flakes. The adsorption of the GF on the GO flakes to create TGF-β3-loaded GO flakes and their subsequent incorporation in the hydrogels through mixing, [(GO/TGF-β3Ads)-F8] hydrogel, led to the upregulation of NP-specific genes, accompained by the production and deposition of an NP-like ECM, rich in aggrecan and collagen II. NP cells actively interacted with TGF-β3-loaded GO flakes and remodeled the scaffolds through endocytosis. This work highlights the potential of using GO as a nanocarrier for the design of functional hybrid peptide-based hydrogels.

Graphene Oxide Ameliorates the Cognitive Impairment Through Inhibiting PI3K/Akt/mTOR Pathway to Induce Autophagy in AD Mouse Model.

Alzheimer's disease (AD) is a neurodegenerative disease of the central nervous system characterised by cognitive impairment. Its major pathological feature is the deposition of β-amyloid (Aβ) peptide, which triggers a series of pathological cascades. Autophagy is a main pathway to eliminate abnormal aggregated proteins, and increasing autophagy represents a plausible treatment strategy against relative overproduction of neurotoxic Aβ. Graphene oxide (GO) is an emerging carbon-based nanomaterial. As a derivative of graphene with neuroprotective effects, it can effectively increase the clearance of abnormally aggregated protein. In this article, we investigated the protective function of GO in an AD mouse model. GO (30mg/kg, intraperitoneal) was administered for 2weeks. The results of the Morris water maze test and the novel object recognition test suggested that GO ameliorated learning and memory impairments in 5xFAD mice. The long-term potentiation and depotentiation from the perforant path to the dentate gyrus in the hippocampus were increased with GO treatment in 5xFAD mice. Furthermore, GO upregulated the expression of synapse-related proteins and increased the cell density in the hippocampus. Our results showed that GO up-regulated LC3II/LC3I and Beclin-1 and decreased p62 protein levels in 5xFAD mice. In addition, GO downregulated the PI3K/Akt/mTOR signalling pathway to induce autophagy. These results have revealed the protective potential of GO in AD.

Graphene oxide enhances β-amyloid clearance by inducing autophagy of microglia and neurons

Alzheimer's disease (AD) is a common neurodegenerative disease, and its pathogenesis is closely related to β-amyloid (Aβ) peptide. The deposition of Aβ in the brain due to impaired Aβ clearance is considered as an important cause of AD. The decrease in Aβ clearance is closely related to the autophagy dysfunction in brains of AD patients. It is feasible to treat AD by increasing the autophagy level of cells such as microglia and neurons to accelerate Aβ clearance. In this article we explored the ability of graphene oxide (GO) to clear Aβ through activating autophagy. Our work demonstrated that GO could inhibit the mTOR signaling pathway by activating AMPK to induce the autophagy of microglial and neurons. As expected, with the improvement of autophagy ability of microglia, GO promoted microglia-mediated Aβ phagocytosis. Under the conditions of co-culture of microglia and neurons, GO induced the autophagy of microglia and neurons, especially the autophagy of microglia, thereby promoting the clearance of Aβ, and ultimately achieved the effect of protecting neurons. Moreover, GO was not only non-cytotoxic to microglia and neurons but also able to reduce the toxicity of Aβ to neurons through its clearance. These results have shown the potential of GO in treating Alzheimer's disease.

Potential of graphene oxide as a drug delivery system for Sumatriptan: a detailed density functional theory study

The adsorption property of Sumatriptan drug onto graphene oxide (GO) was studied using density functional theory (DFT) calculations. All possible initial positions of drug adsorption were considered to find out which one is energetically favorable. According to the achieved findings, the stronger interactions occurred between the positively polarized parts of the Sumatriptan (i.e. hydrogen atoms of the–OH and –NH parts) and negatively polarized oxygen atoms of the GO. The presence of non-covalent interactions of GO and Sumatriptan was confirmed based on the determined geometrical parameters, electronic structure analysis results, and adsorption energies. Different parameters such as frontier molecular orbital (FMO), natural bond orbital (NBO), dipole moment, and solation energy were investigated. Global indices such as hardness, softness, chemical potential, and electrophilicity of all systems were calculated and compared. The adsorption energy values were determined within the range of −8.39 to –10.59 kcal/mol (–1.87 to –5.67 BSSE corrected) in the water solvent for different adsorption geometries. The obtained results show that GO can act as a promising carrier/sensor for Sumatriptan drug in practical application. Communicated by Ramaswamy H. Sarma

A Novel Method for the Removal of Uranium by Using Carboxyl Functionalized Graphene Oxide

Graphene oxide (GO) and functionalized carboxylic graphene oxide (COOH-GO) were successfully synthesized by modified Hummer’s technique. The prepared GO and COOH-GO was characterized successfully by UV-Visible Spectroscopy, Fourier transforms infrared spectroscopy (FTIR), X-ray diffraction, Raman spectroscopy, Scanning electron microscopy (SEM)& Zeta potential. The removal of U(VI) heavy metal comparative study was done by using Graphite, GO & COOH-GO and the removal were confirmed by using LED fluorimeter. The effect of pH of medium, contact time, adsorbent dose, initial concentration of U(VI) were examined for the removal of U(VI). The extent of U(VI) removal has been found to be in the order of COOH-GO >GO> graphite. The U(VI) removal maximum efficiency was observed ~96% observed at pH 4.5. The higher removal efficiency is attributed to the higher negative surface charge of COOH-GO (zeta potential:-39.9 mV) in comparison to zeta potential of GO (-28.9 mV) &graphite (-21.6 mV).

Ductile/brittle PA6/PS system: Effect of carbon nanoplatelets‐modified interface on performance

AbstractAddition of rigid PS to ductile PA6 can lead to higher toughness provided plastic deformation of PS is achieved. The current study deals with upgrading of this system by graphene, graphene oxide (GO), and GO with grafted polystyrene (GO‐g‐PS). Low amount of these carbon nanoplatelets can enhance performance of the PA/PS 90/10 system with the best‐balanced properties achieved with GO‐g‐PS by unique combination of reinforcement with the favorable effect of the GO‐g‐PS‐modified interface on plastic deformation of the PS phase causing higher impact resistance. Simultaneous linking of PA chains and hydrogen bonding causes “anchoring” of PS inclusions in the PA6 phase. This results in support of hydrostatic pressure evolution during loading and thus extensive yielding of PS. Another positive effect is reduction of pullout of in situ formed fibrous inclusions, which is different from rigid short‐fiber composites. The study highlights high potential of GO modified with polymer chains to upgrade polymer systems via tailoring the interface.

Graphene oxide-induced neurotoxicity on neurotransmitters, AFD neurons and locomotive behavior in Caenorhabditis elegans

Graphene oxide (GO) and graphene-based nanomaterials have been widely applied in recent years, but their potential health risk and neurotoxic potentials remain poorly understood. In this study, neurotoxic potential of GO and its underlying molecular and cellular mechanism were investigated using the nematode, Caenorhabditis elegans. Deposition of GO in the head region and increased reactive oxygen species (ROS) was observed in C. elegans after exposure to GO. The neurotoxic potential of GO was then investigated, focusing on neurotransmitters contents and neuronal activity using AFD sensory neurons. The contents of all neurotransmitters, such as, tyrosine, tryptophan, dopamine, tyramine, and GABA, decreased significantly by GO exposure. Decreased fluorescence of Pgcy-8:GFP, a marker of AFD sensory neuron, by GO exposure suggested GO could cause neuronal damage on AFD neuron. GO exposure led decreased expression of ttx-1 and ceh-14, genes required for the function of AFD neurons also confirmed possible detrimental effect of GO to AFD neuron. To understand physiological meaning of AFD neuronal damage by GO exposure, locomotive behavior was then investigated in wild-type as well as in loss-of-function mutants of ttx-1 and ceh-14. GO exposure significantly altered locomotor behavior markers, such as, speed, acceleration, stop time, etc., in wild-type C. elegans, which were mostly rescued in AFD neuron mutants. The present study suggested the GO possesses neurotoxic potential, especially on neurotransmitters and AFD neuron in C. elegans. These findings provide useful information to understand the neurotoxic potential of GO and other graphene-based nanomaterials, which will guide their safe application.

Graphene Oxide Enhances Chitosan-Based 3D Scaffold Properties for Bone Tissue Engineering.

The main goal of bone tissue engineering (BTE) is to refine and repair major bone defects based on bioactive biomaterials with distinct properties that can induce and support bone tissue formation. Graphene and its derivatives, such as graphene oxide (GO), display optimal properties for BTE, being able to support cell growth and proliferation, cell attachment, and cytoskeleton development as well as the activation of osteogenesis and bone development pathways. Conversely, the presence of GO within a polymer matrix produces favorable changes to scaffold morphologies that facilitate cell attachment and migration i.e., more ordered morphologies, greater surface area, and higher total porosity. Therefore, there is a need to explore the potential of GO for tissue engineering applications and regenerative medicine. Here, we aim to promote one novel scaffold based on a natural compound of chitosan, improved with 3 wt.% GO, for BTE approaches, considering its good biocompatibility, remarkable 3D characteristics, and ability to support stem cell differentiation processes towards the bone lineage.

Assessment of graphene oxide ecotoxicity at several trophic levels using aquatic microcosms

Extensive development of new applications using graphene based materials such as graphene oxide (GO) increases its potential release and occurrence into aquatic environments, raising the question of its biological and ecological risks. As standardized single-species-based assays fail to highlight toxicological pathways implying interactions between organisms, the use of micro/mesocosms appears as a good solution to fill the lack of environmental realism inherent to these tests. In this work, experiments were achieved using microcosm systems to expose a reconstituted food chain to GO at environmentally-relevant concentrations (0.05 and 0.1 mg L−1). The trophic chain was composed of a consortium of algae and bacteria as primary producers, chironomid larvae as primary consumers and decomposers while larvae of the amphibian Pleurodeles waltii constituted the secondary consumers. Monitoring of multiple ecotoxicological and ecological endpoints allowed to observe changes in bacterial communities while no toxic effects were noticed in chironomids. However, chironomids feeding behaviour changed as a consequence of GO contamination, leading to an increase in leaf litter consumption. Genotoxic effects were noticed in Pleurodeles larvae. This study highlights the importance of using such experimental systems to better encompass the ecotoxic potential of GO through the determination of toxicological routes and consequences on ecosystem’s functioning.

Enhanced electroluminescent performance by doping organic conjugated ionic compound into graphene oxide hole-injecting layer

Organic conjugated ionic compound 10,10′-dimethyl-9,9′-biacridinum bis(monomethyl terephthalate) (MMT) is doped into graphene oxide (GO) hole-injecting layer to enhance the electroluminescent performance of organic light-emitting diodes (OLEDs). The composite films are characterized in detail by FTIR, SEM, XPS, and UPS. The XPS result indicates the evident π–π stacking interaction between the conjugated structures of GO and MMT. The UPS result shows the decrease in ionization potential of GO due to MMT-doping. As a result, at the optimal doping ratio of 4 wt%, the maximum luminous efficiency of OLEDs is increased to 15.46 cd/A, which is 3.4 times as 4.55 cd/A of the control device. Besides, the luminance is also enhanced to 19950 cd/m2, while the turn-on voltage is decreased to 2.5 V. Doping organic conjugated ionic compound into the GO hole-injecting layer is a facile and efficient approach to improve the electroluminescent performance of OLEDs.

A comparative study for evaluating the performance of five coatings applied on Fe3O4 nanoparticles for inhibition of asphaltene precipitation from crude oil

In this study, potential of Graphene oxide (GO), Silica (SiO2) and Chitosan coatings on Fe3O4 magnetic nanoparticles was investigated for asphaltene adsorption. The comparison between coated and uncoated nanoparticles was made to evaluate the adsorption performance of coatings. The synthesis of nanoparticles was conducted using the co-precipitation method. All nanoparticles were verified using FT-IR, FESEM and XRD analyses. The experiments were performed in two stages. The different parameters effects such as temperature, initial concentration of nanoparticles and initial asphaltene concentration in the synthetic solutions were investigated in the first sets of experiments. Decrease of nanoparticles concentration and temperature and increase in initial asphaltene concentration resulted in increase of asphaltene adsorption capacities. GO-Fe3O4 showed the highest adsorption efficiency followed by chitosan-Fe3O4, Fe3O4 and SiO2-Fe3O4. The average values for adsorption efficiency were 70.47, 66.94, 64.56 and 65.94% for GO-Fe3O4, chitosan-Fe3O4, SiO2-Fe3O4 and Fe3O4 nanoparticles, respectively. In the second stage, the tests with crude oil were performed using the optimum amount of nanoparticles concentration under atmospheric pressure and simulated reservoir conditions. The satisfactory results were obtained for improving adsorption of asphaltenes from crude oil similar to synthetic solution trends. The amount of adsorption increased with increasing pressure. The experimental data for adsorption isotherms models followed the Langmuir model. For adsorption kinetics, the pseudo-second-order Lagergren model showed more precise results. The results showed that we could apply appropriate coatings for inhibition of asphaltene precipitation and enhancement of asphaltene adsorption. However, the asphaltene adsorption amount depends strongly on the kind of coatings applied.