Higher Graphene Oxide Concentrations Research Articles

Immunogenic and toxic effects of graphene oxide nanoparticles in mouse skeletal muscles and human red blood cells

To investigate immunogenic and toxic effects of graphene oxide (GO) nanoparticles in mouse skeletal muscles and in human blood in vitro. GO nanoparticles prepared using a probe sonicator were supended in deionized H2O or PBS, and particle size and surface charge of the nanoparticles were measured with dynamic light scattering (DLS). Different concentrations (0.5, 1.0 and 2.0 mg/mL) of GO suspension or PBS were injected at multiple sites in the gastrocnemius muscle (GN) of C57BL/6 mice, and inflammatory response and immune cell infiltrations were detected with HE and immunofluorescence staining. We also examined the effects of GO nanoparticles on human red blood cell (RBC) morphology, hemolysis and blood coagulation using scanning electron microscope (SEM), spectrophotometry, and thromboelastography (TEG). GO nanoparticles suspended in PBS exhibited better colloidal dispersity, stability and surface charge effects than those in deionized H2O. In mouse GNs, injection of GO suspensions dose- and time-dependently resulted in sustained muscular inflammation and myofiber degeneration at the injection sites, which lasted till 8 weeks after the injection; immunofluorescence staining revealed obvious infiltration of monocytes, macrophages, dendritic cells and CD4+ T cells around the injection sites in mouse GNs. In human RBCs, incubation with GO suspensions at 0.2, 2.0 and 20 mg/mL, but not at 0.002 or 0.02 mg/mL, caused significant alterations of cell morphology and hemolysis. TEG analysis showed significant abnormalities of blood coagulation parameters following treatment with high concentrations of GO. GO nanoparticles can induce sustained inflammatory and immunological responses in mouse GNs and cause RBC hemolysis and blood coagulation impairment, suggesting its muscular toxicity and hematotoxicity at high concentrations.

Fabrication of 3D porous polyurethane-graphene oxide scaffolds by a sequential two-step processing for non-load bearing bone defects

Bone defects as a common orthopedic disease lead to severe pains over a long period. Scaffolds are novel approaches in tissue engineering to treat bone problems and deal with their challenges. Here, 3D porous polyurethane (PU) scaffolds containing graphene oxide (GO) with different percentages (0, 0.1, 0.3, and 0.5 wt%) were developed through a combination of freeze-drying and salt etching techniques for bone tissue engineering applications. The morphologies of scaffolds, physicochemical properties, the degree of crystallinity, and hydrophilicity were evaluated by SEM, FTIR, XRD, and water contact angle assay, respectively. The porosity, degradation behavior, compressive strength, and elastic modulus of 3D porous scaffolds were also determined. To assess the scaffold bioactivity, the morphology of the deposited calcium phosphate layer on the scaffold with macro-structure was evaluated by SEM images. The viability and adhesion of MG63 osteoblast-like cells cultured on the fabricated scaffolds were examined by MTT assay and SEM images, respectively. The results show that adding GO particles not only had no effect on the interconnectivity and porosity of 3D porous macroscopic structures of neat PU but also smaller and more uniformed microscopically pores were obtained. The crystallinity, water contact angle, and weight loss of scaffolds increased as the higher GO concentrations were employed. Followed by increasing GO contents from 0 to 0.5 wt%, the compressive strength and Young’s modulus were increased by 232% and 245%, respectively. The bioactivity of scaffolds was fostered as GO concentration increased. Although, the MTT assay proved the biocompatibility of PU scaffolds containing 0.1 and 0.3 wt% GO, the samples loaded with 0.5 GO had a negative impact on the viability of MG63 cell lines. In conclusion, the present study demonstrates a high potential of PU scaffolds loaded with 0.1 and 0.3 wt% GO particles in bone tissue engineering applications.

Graphene oxide influences transfer of plasmid-mediated antibiotic resistance genes into plants

As an emerging contaminant, antibiotic resistance genes (ARGs) are raising concerns about its significant threat to public health. Meanwhile, graphene oxide (GO), which also has a potential ecological damage with increasingly entering the environment, has a great influence on the transfer of ARGs. However, little is known about the effects mechanisms of GO on the migration of antibiotic resistance genes (ARGs) from bacteria into plants. In this study, we investigated the influence of GO on the transfer of ARGs carried by RP4 plasmids from Bacillus subtilis into rice plants. Our results showed that the presence of GO at concentrations ranging from 0 to 400 mg L−1 significantly reduced the transfer of ARGs into rice roots by 13–71 %. Moreover, the migration of RP4 from the roots to aboveground parts was significantly impaired by GO. These effects may be attributed to several factors. First, higher GO concentrations led to low pH in the culture solution, resulting in a substantial decrease in the number of antibiotic-resistant bacteria. Second, GO induced oxidative stress in rice, as indicated by enhanced Evans blue dye staining, and elevated levels of malondialdehyde, nitric oxide, and phenylalanine ammonia-lyase activity. The oxidative stress negatively affected plant growth, as demonstrated by the reduced fresh weight and altered lignin content in the rice. Microscopic observations confirmed the entry of GO into root cells but not leaf mesophyll cells. Furthermore, potential recipients of RP4 plasmid strains in rice after co-cultivation experiments were identified, including Bacillus subtilis, Bacillus amyloliquefaciens, and Bacillus cereus. These findings clarify the influence of GO on ARGs in the bacteria–plant system and emphasize the need to consider its potential ecological risks.

Exploring the Influence of Chemical Conditions on Nanoparticle Graphene Oxide Adsorption onto Clay Minerals.

High concentrations of graphene oxide (GO), a nanoparticle substance with rapid manufacturing development, have the ability to penetrate the soil surface down to the mineral-rich subsurface layers. The destiny and distribution of such an unusual sort of nanomaterial in the environment must therefore be fully understood. However, the way the chemistry of solutions impacts GO nanoparticle adsorption on clay minerals is still unclear. Here, the adsorption of GO on clay minerals (e.g., bentonite and kaolinite) was tested under various chemical conditions (e.g., GO concentration, soil pH, and cation valence). Non-linear Langmuir and Freundlich models have been applied to describe the adsorption isotherm by comparing the amount of adsorbed GO nanoparticle to the concentration at the equilibrium of the solution. Our results showed fondness for GO in bentonite and kaolinite under similar conditions, but the GO nanoparticle adsorption with bentonite was superior to kaolinite, mainly due to its higher surface area and surface charge. We also found that increasing the ionic strength and decreasing the pH increased the adsorption of GO nanoparticles to bentonite and kaolinite, mainly due to the interaction between these clay minerals and GO nanoparticles' surface oxygen functional groups. Experimental data fit well to the non-linear pseudo-second-order kinetic model of Freundlich. The model of the Freundlich isotherm was more fitting at a lower pH and higher ionic strength in the bentonite soil while the lowest R2 value of the Freundlich model was recorded at a higher pH and lower ionic strength in the kaolinite soil. These results improve our understanding of GO behavior in soils by revealing environmental factors influencing GO nanoparticle movement and transmission towards groundwater.

Effects of Graphene Oxide Nanosheets in Freshwater Biofilms.

Graphene oxide (GO) properties make it a promising material for graphene-based applications in areas such as biomedicine, agriculture, and the environment. Thus, its production is expected to increase, reaching hundreds of tons every year. One GO final destination is freshwater bodies, possibly affecting the communities of these systems. To clarify the effect that GO may impose in freshwater communities, a fluvial biofilm scraped from submerged river stones was exposed to a range (0.1 to 20 mg/L) of GO concentrations during 96 h. With this approach, we hypothesized that GO can: (1) cause mechanical damage and morphological changes in cell biofilms; (2) interfere with the absorption of light by biofilms; (3) and generate oxidative stress, causing oxidative damage and inducing biochemical and physiological alterations. Our results showed that GO did not inflict mechanical damage. Instead, a positive effect is proposed, linked to the ability of GO to bind cations and increase the micronutrient availability to biofilms. High concentrations of GO increased photosynthetic pigment (chlorophyll a, b, and c, and carotenoids) content as a strategy to capture the available light more effectively as a response to the shading effect. A significant increase in the enzymatic (SOD and GSTs activity) and low molecular weight (lipids and carotenoids) antioxidant response was observed, that efficiently reduced oxidative stress effects, reducing the level of peroxidation, and preserving membrane integrity. Being complex entities, biofilms are more similar to environmental communities and may provide more accurate information to evaluate the impact of GO in aquatic systems.

Encapsulation of beta-pancreatic cells in a hydrogel based on alginate and graphene oxide with high potential application in the diabetes treatment

Diabetes mellitus (DM) is a chronic metabolic disease. Current therapies, including islet transplantation suffer instant blood mediated inflammatory reaction, nutrition and oxygen supply deficiency. Graphene oxide (GO) has shown to promote proliferation of different cells and alginate-based scaffolds are alternatives for beta-pancreatic cell functional improvement. We developed an alginate-GO based hydrogel that allows encapsulation and supporting beta-pancreatic cell survival. Physicochemical analysis revealed that a high GO concentration contributed to the morphological and chemical modification of the polymer matrix. Further analysis showed that alginate-GO hydrogel presented a more compact structure, less swelling, and lower degradation rate at high GO concentrations. Mechanical analysis revealed similar behaviour to that of the pancreas. Biocompatibility analysis demonstrated a relative increase in viability, proliferation, and cellular respiration due to GO content. 25 µg/mL alginate-GO hydrogel is a potential candidate for cell encapsulation and in vitro studies suggest a low cytotoxic effect in pancreatic cells, and enhanced functional behaviour, which may be favourable for diabetes treatment.Graphical

Bactericidal Action and Industrial Dye Degradation of Graphene Oxide and Polyacrylic Acid-Doped SnO2 Quantum Dots: In Silico Molecular Docking Study.

The present work demonstrates the systematic incorporation of different concentrations of graphene oxide (GO) into a fixed amount of polyacrylic acid (PAA)-doped SnO2 quantum dots (QDs) through a co-precipitation approach. The research aimed to evaluate the catalytic and antibacterial actions of GO/PAA-SnO2 QDs. Moreover, optical properties, surface morphologies, crystal structures, elemental compositions, and d-spacings of prepared QDs were examined. X-ray diffraction patterns revealed the tetragonal configuration of SnO2, and the crystallinity of QDs was suppressed upon dopants verified by the SAED patterns. Electronic spectra identified the blue shift by incorporating GO and PAA led to a reduction in band gap energy. Fourier transform infrared spectra showed the existence of rotational and vibrational modes associated with the functional groups during the synthesis process. A drastic increase in the catalytic efficacy of QDs was observed in the neutral medium by including dopants, indicating that GO/PAA-SnO2 is a promising catalyst. GO/PAA-SnO2 showed strong bactericidal efficacy against Escherichia coli (E. coli) at higher GO concentrations. Molecular docking studies predicted the given nanocomposites, i.e., SnO2, PAA-SnO2, and GO/PAA-SnO2, as potential inhibitors of beta-lactamaseE.coli and DNA gyraseE.coli.

Swelling and Antimicrobial Activity Characterization of a GO-Reinforced Gelatin-Whey Hydrogel.

Whey-based hydrogel samples with increasing concentrations of graphene oxide (GO) were studied, against a control sample (M), for swelling behavior in light of nuclear magnetic resonance (NMR) and mathematical models of the diffusion process and for antibacterial activity. Graphene oxide (GO) is an optimal filler for whey-based hydrogels, giving them improved mechanical and swelling properties at low concentrations. Crosslinking induces a certain stiffness of the hydrogels, which is why only the first part of the swelling process (<60%) follows the first-order model, while during the whole time interval, the swelling process follows the second-order diffusion model. The NMR relaxometry results are consistent with the swelling behavior of GO-reinforced whey-gelatin composite hydrogels, showing that higher GO concentrations induce a higher degree of cross-linking and, therefore, lower swelling capacity. Only hydrogel samples with higher GO concentrations demonstrated antibacterial activity.

Graphene oxide disruption of homeostasis and regeneration processes in freshwater planarian Dugesia japonica via intracellular redox deviation and apoptosis

The aquatic system is a major sink for engineered nanomaterials released into the environment. Here, we assessed the toxicity of graphene oxide (GO) using the freshwater planarian Dugesia japonica, an invertebrate model that has been widely used for studying the effects of toxins on tissue regeneration and neuronal development. GO not only impaired the growth of normal (homeostatic) worms, but also inhibited the regeneration processes of regenerating (amputated) worms, with LC10 values of 9.86 mg/L and 9.32 mg/L for the 48-h acute toxicity test, respectively. High concentration (200 mg/L) of GO killed all the worms after 3 (regenerating) or 4 (homeostasis) days of exposure. Whole-mount in situ hybridization (WISH) and immunofluorescence analyses suggest GO impaired stem cell proliferation and differentiation, and subsequently caused cell apoptosis and oxidative DNA damage during planarian regeneration. Mechanistic analysis suggests that GO disturbed the antioxidative system (enzymatic and non-enzymatic) and energy metabolism in the planarian at both molecular and genetic levels, thus causing reactive oxygen species (ROS) over accumulation and oxidative damage, including oxidative DNA damage, loss of mitochondrial membrane integrity, lack of energy supply for cell differentiation and proliferation leading to retardance of neuron regeneration. The intrinsic oxidative potential of GO contributes to the GO-induced toxicity in planarians. These data suggest that GO in aquatic systems can cause oxidative stress and neurotoxicity in planarians. Overall, regenerated tissues are more sensitive to GO toxicity than homeostatic ones, suggesting that careful handling and appropriate decisions are needed in the application of GO to achieve healing and tissue regeneration.

Graphene oxide decreases the abundance of nitrogen cycling microbes and slows nitrogen transformation in soils

Graphene oxide (GO) has been widely used in many applications due to its excellent properties. Given the extensive production and use of this nanomaterial, its release into the environment is inevitable. However, little is known about the effects of GO on microbial nitrogen transformation and the related processes after GO enters the soil environment. The present study showed that GO significantly reduced soil microbial biomass and caused a decline in microbial diversity after the soils were subjected to various GO concentrations (10, 100, and 1000 mg kg−1) for 4 months. Among them, the abundances of nitrogen transformation related bacteria such as Firmicutes, Nitrospirota, Proteobacteria, Planctomycetota, and Cyanobacteria were significantly decreased with GO incubation. Among the enzymes that are related to nitrogen transformation, nitrate reductase was the most sensitive even at low concentrations of GO, followed by ammonia monooxygenase and urease, which were reduced by 13–31%, 5–26%, and 9–19% respectively, than those of the control. We found that high concentrations of GO significantly increased the retention of soil urea by 32–59%, and the contents of ammonium and nitrate were 22–28% and 55–69% lower compared to those of the control, respectively. Moreover, the response of most of the indicators in the above process to multilayer GO was more significant than that to single layer GO. Overall, this study provides new insights into the comprehensive understanding of GO's impacts on the soil nitrogen cycle.

Tromethamine functionalized nanocellulose/reduced graphene oxide composite hydrogels with ultrahigh gravimetric and volumetric performance for symmetric supercapacitors

Due to poor pseudocapacitive properties and low packing density, pristine graphene-based supercapacitors have always exhibited inferior gravimetric and volumetric electrochemical performance. Herein, tromethamine functionalized nanocellulose/reduced graphene oxide composites hydrogels (TNGHs) with dense porous structure and high packing density are produced using a one-pot hydrothermal technique. During the reaction, a high-concentration of graphene oxide (GO) solution is used to increase the compactness of the sample. At the same time, tromethamine is used as reducing agent, nitrogen dopant and structure regulator. Furthermore, nanocellulose (NC) can not only be employed as spacers to constrain the extreme agglomeration of graphene, but also be used as reservoirs to boost the diffusion efficiency of electrolytes in the sample. Benefitting from the dense porous structure, pseudocapacitive behavior of the highly-enriched heteroatom functional groups and high packing density, the binder-free symmetric supercapacitors based on TNGH-40 displays ultrahigh gravimetric specific capacitance (342.5 F g−1) and volumetric specific capacitance (339.1 F cm−3) at 0.3 A g−1. This innovative strategy makes TNGHs a potential candidate for miniaturized and compact energy storage devices.

Fluorescence study of the influence of centrifugation on graphene oxide dispersions in water and in tannic acid

Graphene oxide (GO) is acquiring a great interest in biomedicine, biotechnology and biochemistry due to its unique properties. However, GO layers are boundbyvan der Waals forces, which results in aggregation. An efficient dispersion of the aggregated nanostructures is crucial from an application viewpoint, hence eco-friendly procedures are pursued. In this work, the potential of tannic acid (TA) as a GO dispersant in water has been investigated for the first time. Transmission electronic microscopy (TEM) was used to visualize the degree of GO exfoliation in the dispersions. To further assess TA dispersant capability, a fluorescent biomolecule, riboflavin, has been selected. GO and TA cause a quenching effect on riboflavin fluorescence, which depends on the GO and TA concentration, the GO/TA weight ratio and the final centrifugation step that was found to be crucial. Multiple regression analysis has been used to determine the quenching constants for TA and GO simultaneously. The GO-riboflavin interaction weakens upon centrifugation. This step, traditionally used to remove the nanomaterial aggregates, should be avoided to obtain a high GO concentration in the dispersions. This study paves the way towards the use of environmentally friendly dispersant agents instead of conventional organic solvents or synthetic surfactants to attain high-quality dispersions of carbon nanomaterials in water.

Experimental and first-principles study of the interactions between graphene oxide and carbon nanotube

The interaction between carbon nanotubes (CNTs) and graphene oxide (GO) was studied by experimental characterization and first-principle calculation by considering the effect of the functional groups, the chirality of CNT and the contact area between CNT and GO. The results demonstrated that the dispersibility of CNTs can be effectively improved by GO addition. A higher GO concentration results in a better CNT dispersion. The epoxy group is the preferred functional group with the highest Eint, followed by hydroxyl group. The hybridization between C p-O p orbital to form an ionic bond is the primary interaction to strengthen the adhesion between CNT and the epoxy group. For the hydroxyl and carboxyl groups, the interaction between CNT and the functional groups is ascribed to the characteristics of the C-H covalent bonds. The dispersion effect of GO on ac-CNT is more obvious than that of zz-CNT. The contact area between GO and CNT has a more significant impact on the interaction compared with the functional groups. Increasing the contact area is beneficial to improve the interaction between CNT and GO.

Efficiency of marketable decontamination agent and graphene oxide on 99mTc and 131I spillages in nuclear medicine department

Dealing with open sources of radioactive substances in nuclear medicine is a daily task since contamination due to radioactive spills may happen frequently. Proper and safe decontamination management is a vital procedure. However, regular purchase of decontamination agents incurs high costs and might be toxic due to their chemical properties. The purpose of this study is to compare graphene oxide, which is an environmentally friendly carbon-based material and marketable decontamination agent, in decontaminating radioactive spillage. Samples of pure 99mTc and 131I from the laboratory were spilled on a petri dish. The spill was immediately decontaminated with a marketable decontamination agent swab and varying concentrations of graphene oxide swab. The initial radioactivity of each swab containing 99mTc and 131I was measured using a dose calibrator. The absorbance spectra of each sample were analysed using an ultraviolet-visible spectrophotometer. The morphology image of graphene oxide was observed under field emission scanning electron microscope. For decontamination using a marketable decontamination agent, the radioactivity of 131I was slightly higher, whereas that of 99mTc was slightly lower than the high concentration of graphene oxide. The absorbance spectra of 99mTc and 131I that had been decontaminated using graphene oxide were observed at a range of 200 nm to 250 nm due ???* to the transition.

The effect of graphene oxide on thermomechanical and permeability properties of poly(dimethyl siloxane) composites

The effect of graphene oxide (GO) on the properties of composites withhydroxyl-terminated poly(dimethyl siloxane) (PDMS) matrices, prepared by solution mixing, using tetrahydrofuran (THF) as a solvent, were examined. Viscosity measurements during the vulcanization reaction, usinga Brookfield viscosimeter, revealed that GO increases the viscosity of the system, in comparison with the unreinforced PDMS, proportionally to its concentration. The calculation of D and G bands ratio (ID/IG) at 1350 and 1580 cm−1 respectively, using RAMAN spectroscopy, showed more defects in graphene nanoplatelets incorporated in the PDMS nanocomposites. By Differential Scanning Calorimetry (DSC), a slight decrease in glass transition and melting temperatures of PDMS was observed. The thermal stability of composites was significantly improved, especially at higher GO concentrations (0.5 and 1 phr), as it was detected by thermogravimetric analysis (TGA). Also, the tensile strength of composites was enhanced, up to 113%, for samples reinforced with 1 phr GO. The elongation at break was increased, whereas no effect on the modulus of elasticity was observed. A decrease in oxygen permeability of 38% and 15% was measured in membranes made ofcomposites containing 0.5 phr and 1 phr GO respectively. The increase in swellingafter immersion of composites in toluene was explained by the fact that this phenomenon is not only related with the crosslinking density of the elastomer but alsowith the increased absorption properties of GO particles, due to the sonication treatment in THF during the preparation process of the composite, which might contribute to this effect.

Porous-coral-like cerium doped tungsten oxide/graphene oxide micro balls: A robust electrochemical sensing platform for the detection of antibiotic residue

Metal oxides decorated carbon nanomaterials, as an electrode material have been well explored in the field of electrochemical sensor. However, instead of using the high concentration of graphene oxide (GO), we try to explore the influence of minimum quantity of GO in material synthesis. Here we demonstrate the hydrothermal synthesis of low-cost cerium (Ce)-doped tungsten oxide/graphene oxide (CeW/GO) composite for the precise electrochemical detection of antibiotic drug furazolidone (FUZ). For the synthesis of composite, 40 μg/mL concentration of GO has been utilized. Then, several physicochemical and electrochemical techniques were used to examine the morphological, structural, and electrochemical characteristics of the CeW/GO composite. Interestingly, the composite material has a porous-coral-like structure, which is being described here for the first time. The GO nanosheets cover the CeW and make the smooth surface and lead to the porous structure. Then we looked into the analytical behavior of CeW/GO composite modified glassy carbon electrode for the application towards the electrochemical detection of the FUZ using the voltammetric technique. The effect of experimental conditions, including loading concentration of active material, pH, scan rate, accumulation time, and concentration of FUZ, were analyzed with respect to the reduction peak current response of FUZ. At the optimum conditions, the fabricated sensor has a low detection limit (0.054 μM), appreciable sensitivity (2.5 μA μM −1 cm −2 ) with a wide linear range (1–260 μM), and the decent anti-interference ability for FUZ detection. Furthermore, the developed sensor was successfully used to assess the FUZ concentration in the human urine samples, yielding satisfactory results. • porous-coral-like CeW/GO micro balls composite material was designed for the first time. • The CeW/GO composite was employed as a novel electrocatalyst to detect the furazolidone (antibiotic drug). • A detailed study was made on electrochemical performance of the developed sensor. • The performance of CeW/GO/GCE was comparable with the noble metals (Pt, Re, and Au) based modified electrodes.

Integrating transcriptome and physiological analyses to elucidate the molecular responses of buckwheat to graphene oxide

With the increasing application of nanomaterials, evaluation of the phytotoxicity of nanoparticles has attracted considerable interest. Buckwheat is an economically pseudocereal crop, which is a potential model for investigating the response of plants to hazardous materials. In this study, the response of buckwheat to graphene oxide (GO) was investigated by integrating physiological and transcriptome analysis. GO can penetrate into buckwheat root and stem, and high concentrations of GO inhibited seedlings growth. High concentration of GO improved ROS production and regulated the activities and gene expression of oxidative enzymes, which implying GO may affect plant growth via regulating ROS detoxification. Root and stem exhibit distinct transcriptomic responses to GO, and the GO-responsive genes in stem are more enriched in cell cycle and epigenetic regulation. GO inhibited plant hormone biosynthesis and signaling by analyzing the expression data. Additionally, 97 small secreted peptides (SSPs) encoding genes were found to be involved in GO response. The gene expression of 111 transcription factor (TFs) and 43 receptor-like protein kinases (RLKs) were regulated by GO, and their expression showed high correlation with SSPs. Finally, the TFs-SSPs-RLKs signaling networks in regulating GO response were proposed. This study provides insights into the molecular responses of plants to GO.

Effects of Graphene Oxide on Germination and Early Growth of Plants.

Owing to its excellent material properties such as large surface area and superb mechanical and thermal characteristics, graphene oxide (GO) is likely to be applied in a variety of environmental fields. These applications may lead to the entrance of GO in terrestrial ecosystems, but there is little research regarding the impact of GO on plants upon such entrances. To analyze the effects of GO on the germination and growth of various plants, the changes in lettuce, radish, perennial ryegrass, alfalfa, and cucumber seeds under GO treatment was studied. Germination rate and growth were analyzed after the seeds were exposed to GO at 0, 0.2, 0.4, 0.8, and 1.6 mg ml-1. For lettuce, the germination rate decreased with GO concentration. However, no significant effects were observed on the germination rate of other plants. On the other hand, the growth of lettuce, alfalfa, and radish decreased under GO treatment. For example, at 1.6 mg ml-1 of GO, the length of shoot and root of lettuce was shortened by 87% and 86%, respectively. Such results indicate that the germination and early growth of plants can be negatively affected in a species-specific manner under high concentrations of GO. Hence, we anticipate that our results may assist in supplementing the legal regulations for the proper disposal of nanomaterials.

The promotion and inhibition effect of graphene oxide on the process of microbial denitrification at low temperature

This study found that graphene oxide (GO) improved microbial denitrification at low temperatures (~12 °C), and the optimal concentration was 10 mg/L as the removal rate of NO3-N increased by 17%. At the optimal concentration, GO improved the electron transport system activity of the microbes and enhanced the activity of nitrate reductase and nitrite reductase while exhibited low microbial toxicity. The addition of GO increased the content of tightly bound extracellular polymeric substances (EPS). The results of fluorescence spectrometer indicated that GO accelerated the renewal of bound EPS (B-EPS). Fourier Transform infrared spectroscopy (FTIR) results showed that GO affected the secondary structure of the protein in B-EPS, making B-EPS more hydrophobic and promoting microbial aggregation. B-EPS affected by GO can promote the electron transfer process of microorganisms. However, high concentration (>25 mg/L) of GO may inhibit denitrification by competing for electrons, which was not conducive to denitrification thermodynamically.

Performance and responses of aerobic granular sludge at different concentrations of graphene oxide after a single administered dose.

To investigate the impact of graphene oxide (GO) under different concentrations (0, 50, 100, 150, and 200mg/L) on aerobic granular sludge (AGS) after a single administered dose, the performance of nitrogen removal, microbial enzymatic activity, extracellular polymeric substances (EPSs), and microbial community structure was analyzed in batch tests. The results showed that the impact of GO concentrations on AGS was dose- and time-dependent. Short-term GO exposure could accelerate the nitrification process of AGS, while relatively concentrations (≥100mg/L) inhibited the process when present for extended periods of time. The microbial enzymatic activity showed similar tendency. The production of lactate dehydrogenase release (LDH) in 200mg/L group was increased 48.04% and EPS contents decreased 30.06% compared to the control group at 30th day and showed that high concentrations of GO have toxic effects on AGS. The microbial bacteria responded differently to the stimulation of different concentrations of GO. PRACTITIONER POINTS: GO affected AGS system performance in concentration- and time-dependent manners. The nitrification rate of AGS increased in the short term and reversed over time. Long-term exposure to high GO concentrations caused toxicity to AGS. Different microorganisms had diverse responses to GO concentrations.