Graphene Oxide Surface Research Articles

Upgraded and Light-Up Biosensing Platform: Entropy-Driven Catalysis Circuit Manipulates the Configuration Transformation of Novel DNA Silver Nanoclusters on the Graphene Oxide Surface.

To tackle the predicament of the traditional turn-off mechanism, exploring an activated turn-on system remains an intriguing and crucial objective in biosensing fields. Herein, a dark DNA Ag nanocluster (NC) with hairpin-structured DNA containing a six-base cytosine loop (6C loop) as a template is atypically synthesized. Intriguingly, the dark DNA Ag NCs can be lit to display strong red-emission nanoclusters. Building upon these exciting findings, an unprecedented and upgraded turn-on biosensing system [entropy-driven catalysis circuit (EDCC)-Ag NCs/graphene oxide (GO)] has been created, which employs an EDCC to precisely manipulate the conformational transition of DNA Ag NCs on the GO surface from adsorption to desorption. Benefiting from the effective quenching of GO and signal amplification capability of the EDCC, the newly developed EDCC-Ag NCs/GO biosensing system displays a high signal-to-background (S/B) ratio (26-fold) and sensitivity (limit of detection as low as 0.4 pM). Meanwhile, it has good specificity, excellent stability, and reliability in both buffer and biological samples. To the best of our knowledge, it is the first example that adopts an EDCC to precisely modulate the configuration transformation of DNA Ag NCs on the GO surface to obtain a biosensor with low background, strong fluorescence, high contrast, and sensitivity. This exciting finding may provide a new route to fabricate a novel turn-on biosensor based on hairpin-templated DNA Ag NCs in the optical imaging and bioanalytical fields.

Effect of DBSA‐doped PANI on the corrosion protection performance of GO/epoxy coatings

AbstractIn this study, the anticorrosion effect of polyaniline doped with dodecyl benzene sulfonic acid (PANI‐DBSA) in graphene oxide (GO)/epoxy coating is investigated. PANI‐DBSA is effectively synthesized on the surface of GO via chemical polymerization, and its properties are investigated via a series of characterization methods. The PANI‐DBSA/GO hybrid exhibits improved compatibility with organic resin. The anticorrosion performance of PANI‐DBSA/GO coatings is assessed through water absorption tests, electrochemical impedance spectroscopy measurements, and adhesion strength tests. The results indicate that PANI reduces the water absorption of GO, and the favorable compatibility of PANI‐DBSA/GO with epoxy resin minimizes coating defects and enhances the interfacial blocking for diffusion electrolytes. In this work, the PANI has no active function such as passivating the metal surface, it just serves to shield the hydrophilic GO surface and to improve compatibility between GO and the epoxy, attributing its low pigment content.

Porous Agarose Layered Magnetic Graphene Oxide Nanocomposite for Virus RNA Monitoring in Wastewater.

The detection of virus RNA in wastewater has been established as a valuable method for monitoring Coronavirus disease 2019. Carbon nanomaterials hold potential application in separating virus RNA owing to their effective adsorption and extraction capabilities. However, carbon nanomaterials have limited separability under homogeneous aqueous conditions. Due to the stabilities in their nanostructure, it is a challenge to efficiently immobilize them onto magnetic beads for separation. Here, we develop a porous agarose layered magnetic graphene oxide (GO) nanocomposite that is prepared by agglutinating ferroferric oxide (Fe3O4) beads and GO with agarose into a cohesive whole. With an average porous size of approximately 500 nm, the porous structure enables the unhindered entry of virus RNA, facilitating its interaction with the surface of GO. Upon the application of a magnetic field, the nucleic acid can be separated from the solution within a few minutes, achieving adsorption efficiency and recovery rate exceeding 90% under optimized conditions. The adsorbed nucleic acid can then be preserved against complex sample matrix for 3 days, and quantitatively released for subsequent quantitative reverse transcription polymerase chain reaction (RT-qPCR) detection. The developed method was successfully utilized to analyze wastewater samples obtained from a wastewater treatment plant, detecting as few as 10 copies of RNA molecules per sample. The developed aMGO-RT-qPCR provides an efficient approach for monitoring viruses and will contribute to wastewater-based surveillance of community infections.

Distinct ion transport behavior between graphene oxide and UV-irradiated reduced graphene oxide membranes

Graphene oxide (GO) membranes are promising materials for achieving selective ion permeation in aqueous solutions. However, the swelling of GO laminates, caused by the affinity of water molecules for oxygen-containing groups (OCGs) on GO, significantly limits the practical prospects of GO membranes for selective ion transport and separation applications. Selectively removing OCGs from GO has been shown to decrease the interlayer distance between individual GO sheets, thereby improving the ability of laminate membranes to discriminate between different ions based on a size-exclusion mechanism. In this work, GO reduced through exposure to ultraviolet light (UV-rGO) is shown to display ion transport behavior that raises questions about size-exclusion as the dominant mechanism determining selective ion transport in GO membranes. Notably, smaller monovalent Li+ cations are found to permeate more slowly through UV-rGO membranes than larger divalent metal cations such as Ca2+ and Mg2+. This unexpected behavior results in a 3 – 4 fold improvement in the separation selectivity between these representative cations with UV-rGO compared to pristine GO membranes. Through a joint experimental and theoretical study, we identified the factors influencing selective ion transport through the nanochannels in UV-rGO membranes. We demonstrate that the selective removal of hydroxyl (–OH) groups from the basal planes of GO enhances the interactions of metal cations with functional groups located at the edges of GO, thereby resulting in a lower ratio of free Li+ in solution, rather than stationary Li+ adsorbed onto the surface GO, compared to Ca2+ cations. Based on these results, we propose a separation mechanism analogous to chromatography, which emphasizes the crucial role of different OCGs on GO surfaces in controlling selective ion transport through GO membranes.

Radiation-induced preparation of nanoscale CoO@graphene oxide for activating peroxymonosulfate to degrade emerging organic pollutants

In this study, ionizing radiation was used to induce the in-situ formation of highly dispersed nanosized cobalt oxide on the surface of graphene oxide (R-Co-GO), which was highly effective for activating PMS to degrade sulfamethoxazole (SMX). R-Co-GO had the highest catalytic activity when 150 μL cobalt chloride hexahydrate solution was used in the precursor, and the pseudo first-order kinetic constant of SMX degradation was 0.07 min−1 with high mineralization efficiency (63.1 %) and high PMS utilization efficiency. The sulfate radicals and high-valent cobalt oxo were mainly responsible for SMX degradation. Mechanism analysis showed that cobalt active site dominated in PMS activation, which was responsible for the formation of sulfate radicals and high-valent cobalt oxo; while the carbon framework contributed to the formation of singlet oxygen. The R-Co-GO-150 had good catalytic activity and stability in five cycling experiments, in which SMX was completely degraded and the concentration of dissolved Co was below 0.1 mg/L. In addition, the R-Co-GO-150/PMS system could also degrade phenol, bisphenol A, atrazine and nitrobenzene effectively, confirming its wide applicability. This study provided a facile method to uniformly disperse the metal oxides on the surface of carbon materials, and an effective system for the removal of emerging organic pollutants from the actual wastewater.

Reduction of graphene oxide film on glass substrate using argon ion beam irradiation: A systematic study with X-ray photoelectron spectroscopy analysis

In our research, we explored a novel and eco-friendly method of utilizing argon ion beam irradiation to thin down graphene oxide (GO) films on glass substrates, aiming to enhance their mechanical, electrical, and optical properties. By employing high-energy argon ions, we developed a groundbreaking, environmentally conscious technique that not only permits micro-patterning directly on GO films but also facilitates concurrent material characterization. Varying the energy levels (1000, 2000, and 3000 eV) and exposure times (0 to 80 s, in 20-second increments), we meticulously examined the impact on carbon and oxygen atomic ratios of the GO using X-ray photoelectron spectroscopy (XPS) for in-depth analysis. Our findings revealed that increasing the argon ion beam energy to 2000 eV and extending the irradiation time significantly reduced oxygen content while increasing the carbon atomic ratio, indicating effective GO surface reduction. However, further increasing the energy to 3000 eV resulted in a slight increase in oxygen content and a decrease in the carbon atomic ratio compared to the energy 2000 eV, suggesting a decrease in reduction efficacy. This method's simplicity, eco-friendliness, and precision mark a significant advancement over traditional chemical reduction methods, offering a solid understanding of high-energy argon ion beam irradiation's effectiveness in GO reduction. Our comprehensive analysis, including survey and high-resolution C 1s and O 1s XPS spectra, highlights the surface chemistry modifications induced by this treatment, demonstrating the versatility of argon ion beam irradiation in producing reduced graphene oxide (rGO) for various applications.

Adsorption of fast green dye onto Fe3O4 MNPs and GO/Fe3O4 MNPs synthesized by photo-irradiation method: Isotherms, thermodynamics, kinetics, and reuse studies

In this study, the adsorption of Fast Green dye (FGD) on the surface of ferrous ferric oxide Fe3O4 MNPs and Graphene oxide Nano-Sheets/ferrous ferric oxide GO/Fe3O4 MNPs as adsorbents was examined. The photo-irradiation method was successfully used to synthesize Fe3O4 MNPs and GO/Fe3O4 MNPs using UV lamp. Raman spectroscopy was used to characterize the GO and GO/ Fe3O4 MNPs. XRD, FESEM, and EDX were used to characterize the Fe3O4 MNPs and GO/ Fe3O4 MNPs. Optimal adsorption conditions were studied, including a contact time of 60 min, MNPs amount of 0.05 g, pH 2, FGD concentration of 10 mg/L, and temperature of 308 K. Langmuir, Freundlich, Temkin, and Dubinin–Radushkevich (D-R) isotherm models were used to fit the experimental equilibrium data at five different temperatures (288, 298, 308, 318, and 328 K). It was noticed that FGD adsorption on Fe3O4 MNPs and GO/ Fe3O4 MNPs is consistent with the Freundlich model at 308 K. The PSO rate kinetics suggests that both MNPs are promising materials for the removal of FGD from aqueous solutions. Thermodynamic studies showed that the adsorption processes are non-spontaneous on both MNPs surfaces, endothermic for Fe3O4 MNPs, and exothermic for GO/ Fe3O4 MNPs. All the results confirm that Fe3O4 MNPs and GO/ Fe3O4 MNPs have the potential to be efficient, low-cost, reusable, and stable adsorbents for the removal of FGD from aqueous solutions.

In situ growth of covalent organic framework on graphene oxide nanosheet enable proton-selective transport in flow battery membrane

Perfluorosulfonic acid (PFSA) is the most widely used membrane material for all-vanadium redox flow batteries (VRFB). However, severe vanadium ion permeation of PFSA membranes remains to be solved. In this work, a series of PFSA-based composite membranes are prepared by introducing two-dimensional continuous covalent organic framework (COF) to achieve enhanced performance. Two dimensional continuous Schiff base network-type COFs (GO/SNW) are synthesized by using the two-dimensional multi-functionalized surface of graphene oxide (GO) as a reaction site. Compared to the original form of agglomerated particles, two-dimensional continuous structure obtained a larger vanadium resistance area. Comparing to conventional PFSA membranes, the special pores of COF have a size sieving mechanism for selectively proton transfer, leading to simultaneously enhancement of proton conductivity and vanadium barrier property. VRFB assembled with PFSA-GO/SNW-7 showed high Coulombic efficiency (CE: 97.47%–98.18 % VS PFSA: 80.73%–91.92 %) and energy efficiency (EE: 93.04%–85.71 % VS PFSA: 77.53%–81.78 %) at 40–120 mA cm−2. In addition, there is no significant decrease in the efficiency of battery assembled with PFSA-GO/SNW-7 after 800 cycle (than 650 h) tests. This work provides a new direction in the design of fillers for mixed matrix membranes.

Amino Group-Driven Adsorption of Sodium p-Perfluorous Nonenoxybenzene Sulfonate in Water by the Modified Graphene Oxide.

Sodium p-perfluorous nonenoxybenzene sulfonate (OBS) is one of the key alternatives to perfluoroalkyl substances (PFASs). Its widespread tendency has increased extensive contamination in the aquatic environment. However, the present treatment technology for OBS exhibited insignificant adsorption capacity and long adsorption time. In this study, three proportions (1:5, 3:5, and 10:1) of chitosan-modified amino-driven graphene oxide (CS-GO) were innovated to strengthen the OBS adsorption capacity, compared with graphene oxide (GO) and graphene (GH). Through the characterization of SEM, BET, and FTIR, it was discovered that CS was synthetized on GO surfaces successfully with a low specific surface area. Subsequently, batch single influence factor studies on OBS removal from simulated wastewater were investigated. The optimum removal efficiency of OBS could be achieved up to 95.4% within 2 h when the adsorbent was selected as CS-GO (10:1), the dosage was 2 mg, and the pH was 3. The addition of inorganic ions could promote the adsorption efficiency of OBS. In addition, CS-GO presented the maximum adsorption energy due to additional functional groups of -NH3, and electrostatic interaction was the foremost motive for improving the adsorption efficiency of OBS. Moreover, OBS exhibited the fastest diffusion coefficient in the CS-GO-OBS solution, which is consistent with the fitting results of adsorption kinetics.

Using Sandwiched Silicon/Reduced Graphene Oxide Composites with Dual Hybridization for Their Stable Lithium Storage Properties.

Using silicon/reduced graphene oxide (Si/rGO) composites as lithium-ion battery (LIB) anodes can effectively buffer the volumetric expansion and shrinkage of Si. Herein, we designed and prepared Si/rGO-b with a sandwiched structure, formed by a duple combination of ammonia-modified silicon (m-Si) nanoparticles (NP) with graphene oxide (GO). In the first composite process of m-Si and GO, a core-shell structure of primal Si/rGO-b (p-Si/rGO-b) was formed. The amino groups on the m-Si surface can not only hybridize with the GO surface to fix the Si particles, but also form covalent chemical bonds with the remaining carboxyl groups of rGO to enhance the stability of the composite. During the electrochemical reaction, the oxygen on the m-Si surface reacts with lithium ions (Li+) to form Li2O, which is a component of the solid-electrolyte interphase (SEI) and is beneficial to buffering the volume expansion of Si. Then, the p-Si/rGO-b recombines with GO again to finally form a sandwiched structure of Si/rGO-b. Covalent chemical bonds are formed between the rGO layers to tightly fix the p-Si/rGO-b, and the conductive network formed by the reintroduced rGO improves the conductivity of the Si/rGO-b composite. When used as an electrode, the Si/rGO-b composite exhibits excellent cycling performance (operated stably for more than 800 cycles at a high-capacity retention rate of 82.4%) and a superior rate capability (300 mA h/g at 5 A/g). After cycling, tiny cracks formed in some areas of the electrode surface, with an expansion rate of only 27.4%. The duple combination of rGO and the unique sandwiched structure presented here demonstrate great effectiveness in improving the electrochemical performance of alloy-type anodes.

Electrochemical polymerization of PEDOT:PSS with graphene oxide and silver nanoparticles for antibacterial coating and SERS detection

This study involved the use of electrochemical polymerization to coat poly(3,4-ethylenedioxythiophene) (PEDOT), polystyrene sulfonate (PSS) and graphene oxide (GO) onto SUS316L stainless steel substrates, aiming to produce PEDOT:PSS and GO@PEDOT:PSS films. Following this, Ag@PEDOT:PSS and GO/Ag@PEDOT:PSS films were developed through the electrochemical deposition of silver nitrate. Electrochemical impedance spectroscopy (EIS) indicated that adding GO increased the impedance of film, while AgNPs deposition decreased it, thereby enhancing conductivity. Films with AgNPs showed surface enhanced Raman scattering (SERS) effects, as assessed using malachite green (MG). Compared to films without GO, the GO/Ag@PEDOT:PSS films exhibit enhanced conductivity and SERS detection performance due to the negatively charged functional groups on the GO surface forming a continuous layer of AgNPs. Moreover, antibacterial capabilities were evaluated through bacterial attachment and inhibition zone assays. Both Ag@PEDOT:PSS and GO/Ag@PEDOT:PSS films were effective in inhibiting bacterial adhesion, achieving up to 99.4 % and 99.0 % inhibition, respectively. In the inhibition zone assays, the GO/Ag@PEDOT:PSS film showed a 1.33 times increase in antibacterial efficacy compared to Ag@PEDOT:PSS. Furthermore, the effectiveness of electrodepositing antibiotics on these substrates was investigated, confirming optimal antibacterial performance. This efficacy is attributed to the synergistic interaction between silver nanoparticles and antibiotics, potentially reducing the need for antibiotics. The findings of this study highlight its significant potential for applications in antibacterial treatments and biomedical detection.

Manganese(II)-Enhanced Graphene Oxide Fluorescence Switch-Based Hybridization Chain Reaction for the Enzyme-Free and Sensitive Determination of Bacillus thuringiensis (Bt) in Transgenic Crops

Bacillus thuringiensis, as a special DNA sequence, has been introduced into crops for insect control. At the same time, the safety risk of transgenic crops has received wide concern. Herein, a simple, enzyme-free and sensitive novel nanosensor for the determination of Bacillus thuringiensis by manganese(II)-enhanced graphene oxide (GO) fluorescence switch (Mn(II)-GO-FS)-based hybridization chain reaction (HCR) signal amplification was developed. The high affinity of Mn(II) to oxygen-containing groups in double-stranded DNA and on the surface of GO was able to overcome the steric effect of rigid double chains and drive the efficient adsorption of HCR hairpin probes with sticky ends on GO. The efficient quenching of 6-carboxyfluorescein (FAM) labeled on the HCR hairpin probes guaranteed a low background. The Bacillus thuringiensis acted as a trigger to initiate a cascade of hybridization events between the two metastable HCR hairpin probes (H1 and H2) to polymerize into a nicked long double-helix structure (dsDNA). The products desorbed from the surface of GO and produced strong fluorescence. The results included a wide linear range (0.1 pM-50 nM) and a low detection limit (0.05 pM). This nanosensor was successfully applied to determine Bacillus thuringiensis in maize seeds with spiked recoveries between 97.5% and 103%. The Mn(II)-GO-FS had a simple design and was conveniently used for the determination of other special genes by changing the corresponding HCR hairpin probe sequence. Moreover, this novel nanosensor did not require harsh experimental conditions, operating in a neutral environment.

Electrochemical Sensor Modified with Graphene Oxide Decorated with Copper Oxide Nanoparticles for Velpatasvir’s Monitoring in Spiked Human Plasma

Velpatasvir, an antiviral agent co-formulated with sofosbuvir used to treat hepatitis C, has recently demonstrated beneficial therapeutic effects against COVID-19. Therefore, therapeutic drug monitoring of velpatasvir is essential to achieve the desired clinical outcomes. An electrochemical sensor modified with synthesized copper oxide nanoparticles on the surface of graphene oxide (CuO/GO-NPs) was fabricated for the analysis of velpatasvir for the first time. Characterization was carried out using Fourier-transform infrared spectroscopy, X-ray diffraction, and scanning electron microscopy with energy-dispersive X-ray spectroscopy. The voltammetric determinations were conducted using differential pulse and cyclic voltammetry, where the modified electrode exhibited better sensitivity than the unmodified one. The method was validated according to the International Council for Harmonisation (ICH) guidelines, exhibiting linearity within a range of 1.0 × 10−7 – 1.0 × 10−5 M, covering velpatasvir’s maximum plasma concentration (Cmax), with a quantification limit of 2.89 × 10−7 M and a detection limit of 9.03 × 10−8 M. The developed sensor was successfully applied to spiked human plasma at velpatasvir’s Cmax level. The method’s greenness was assessed using the Analytical Eco-scale and the Green analytical procedure index tools. This method holds promise as a green simple approach to implemented in future velpatasvir’s therapeutic drug monitoring studies.

Exploring the structure, characteristics, and thermal degradation of composites comprising thermoplastic polyolefin and graphene oxide under high-temperature dynamic shear conditions

Dynamic high-temperature shear aging tests were conducted on thermoplastic polyolefin (TPO)/graphene oxide (GO) composite materials using a Hakke torque rheometer. The study employed ATR-FTIR, DSC, SEM, oxygen performance testing, and TGA to analyze the structure, properties, thermal degradation behavior, kinetics, and mechanisms of TPO/GO composites. The results demonstrated that the high-temperature dynamic shear thermal oxidative aging of TPO/GO composite materials establishes a dual protective mechanism, incorporating physical (intercalation oxygen resistance) and chemical (inorganic oxygen resistance) effects. This can be attributed to the polar surface and honeycomb structure of GO, as well as the shear-induced more uniform physical distribution of GO within TPO. Consequently, TPO/GO composite materials exhibit significantly enhanced resistance to dynamic shear thermal oxidative aging compared to TPO alone.

The synthesis of hyperbranched polysiloxane-functionalized graphene oxide with excellent water lubrication performance

Water, esteemed for its sustainable and environmentally friendly lubricating qualities, faces constraints due to its limited load-bearing capacity and diminished lubrication performance, restricting its applications. This study endeavors to overcome these challenges by synthesizing a hyperbranched polysiloxane (HBPSi) and grafting it onto graphene oxide (GO) surfaces. The remarkable lubricating properties and hydrophilicity of HBPSi enable the stable dispersion of GO in water, thereby enhancing overall lubrication performance. This novel approach not only increases water's carrying capacity but also enhances its lubricating ability. Consequently, the resultant HBPSi-GO exhibits exemplary tribological properties. By elucidating this methodology, our research establishes a practical foundation for the development of high-performance water lubrication additives.

A DFT Study of CO Hydrogenation on Graphene Oxide: Effects of Adding Mn on Fischer–Tropsch Synthesis

The hydrogenation of carbon monoxide (CO) offers a promising avenue for reducing air pollution and promoting a cleaner environment. Moreover, by using suitable catalysts, CO can be transformed into valuable hydrocarbons. In this study, we elucidate the mechanistic aspects of the catalytic conversion of CO to hydrocarbons on the surface of manganese-doped graphene oxide (Mn-doped GO), where the GO surface includes one OH group next to one Mn adatom. To gain insight into this process, we have employed calculations based on the density functional theory (DFT) to explore both the thermodynamic properties and reaction energy barriers. The Mn adatoms were found to significantly activate the catalyst surface by providing stronger adsorption geometries. Our study concentrated on two mechanisms for CO hydrogenation, resulting in either CH4 production via the reaction sequence CO → HCO → CH2O → CH2OH → CH2 → CH3 → CH4 or CH3OH formation through the CO → HCO → CH2O → CH2OH → CH3OH pathway. The results reveal that both products are likely to be formed on the Mn-doped GO surface on both thermodynamic grounds and considering the reaction energy barriers. Furthermore, the activation energies associated with each stage of the synthesis show that the conversion reactions of CH2 + OH → CH3 + O and CH2O + OH → CH2OH + O with energy barriers of 0.36 and 3.86 eV are the fastest and slowest reactions, respectively. The results also indicate that the reactions: CH2OH + OH → CH2 + O + H2O and CH2OH + OH → CH3OH + O are the most exothermic and endothermic reactions with reaction energies of −0.18 and 1.21 eV, respectively, in the catalytic pathways.

A simple chemiluminescent method for the quantification of exosomes based on horseradish peroxidase adsorbed on two-dimensional nanomaterials

The development of simple methods for the isolation and quantification of exosomes in biological samples is important. By using the typical two-dimensional (2D) nanomaterials, graphene oxide (GO), the present work first studied the interaction of liposomes with the nanocomposites formed by adsorbing HRP on the GO surface and found the presence of liposomes led to the release of HRP from the GO surface to the solution phase triggering the luminol-H2O2 chemiluminescence (CL) reaction to emit light. Benefiting from the similarity of exosomes to liposomes in both composition and morphology aspects, the GO-HRP nanocomposites with a mass ratio of 120:1 and 160:1 were employed for the quantitative detection of exosomes in 100-fold diluted serum samples. The whole detection process took about 15 min and as low as 3.2 × 102 particles μL−1 of exosomes could be sensitively detected. In addition to GO-HRP nanocomposites, the CL responses of other nanocomposites obtained from adsorbing HRP on other 2D nanomaterials such as layered MoS2 for exosomes were also tested. MoS2-HRP exhibited similar behavior and the LODs for the detection of exosomes were 5.8 × 102 particles μL−1. The proposed assays were a biomarker-independent quantitative method that achieved the quantification of exosomes in serum samples directly without an isolation process.

Effect of Graphene Oxide Surface Deposition Process on Synthetic Macrofibers and Its Results on the Microstructure of Fiber-Reinforced Concrete.

The improvement of the mechanical properties of concrete can be achieved with the use of synthetic macrofibers. However, this fiber-matrix interaction will be sufficiently efficient for tensile efforts only when there is a binding agent that associates the characteristics of the paste with the characteristics of the surface of the reinforcing material. As already identified, in a first phase of this research using synthetic microfibers, a better fiber-matrix interaction can be achieved with the surface treatment of synthetic fibers with graphene oxide. In this way, we sought to evaluate the surface treatment with graphene oxide on two synthetic polypropylene macrofibers (macrofiber "A" and macrofiber "B") and its contribution to the concrete transition zone. The surface deposition on the macrofiber was carried out using the ultrasonication method; then, the macrofiber with the best deposition for creating reinforced concrete mixtures was identified. To evaluate the quality of GO deposition, scanning electron microscopy (SEM-FEG) and energy-dispersive spectroscopy (EDS) tests were carried out; the same technique was used to evaluate the macrofiber-matrix transition zone. The SEM-FEG images indicated that macrofiber "B" obtained greater homogeneity in surface deposition and it presented a 13% greater deposition of C in the EDS spectra. The SEM-FEG micrographs for reinforced concrete indicated a reduction in voids in the macrofiber-matrix transition zone for concretes that used macrofibers treated with GO.

Nanostructures Originated from Grafting Amino Group Containing Biomolecules on Graphene Oxide

AbstractWith the aim of obtaining new composites from graphene oxide for a new biological application, it urged us to select some amine containing molecules namely purpald, mafenide acetate and fluvoxamine for grafting that was resulted to the formation of purpald‐grafted graphene oxide, mafenide‐grafted graphene oxide and fluvoxamine‐grafted graphene oxide, respectively. These novel nanocomposites were evaluated by X‐ray photoelectron spectroscopy, Transmission electron microscopy, Field emission scanning electron microscopy,Dynamic light scattering, Zeta potential, X‐ray diffraction, Thermogravimetric analysis, Raman, and Fourier‐transform infrared. The findings demonstrated that the grafting was done satisfactorily. X‐ray photoelectron spectroscopy analysis revealed that the peaks seen at 286.07, 285.79, and 285.49 eV corresponded to the formation of carbon‐nitrogen bonds between the amine groups of purpald, mafenide acetate, and fluvoxamine, respectively, and the functionalized oxygen groups present on the surface of graphene oxide. In this study, three nanocomposites were subjected to practical testing in close proximity to human breast cancer cells. After a period of 24 hours, it was shown that purpald‐grafted graphene oxide demonstrated more cellular toxicity compared to the other nanocomposites.

Low-background fluorescent biosensor based on graphene oxide and aptamer biorecognition for sensitive detection of kanamycin

The detection of kanamycin has attracted extensive attention in the field of food safety. A label-free, low-background fluorescent biosensor was successfully constructed based on graphene oxide and aptamer biorecognition in this paper for kanamycin detection in milk samples. In this biosensor, the integrated probe with the aptamer sequence of kanamycin and the G-rich sequence was designed. The aptamer sequence of kanamycin was used as the recognition part, the G-quadruplex/N-methyl mesoporphyrin IX (NMM) complex as the fluorescent probe, and graphene oxide as the fluorescent quencher. Initially, the integrated probe could be adsorbed on the graphene oxide surface through π-π stacking interactions, while the fluorescence of NMM could be efficiently quenched because of the resonance energy transfer between NMM and graphene oxide, which was beneficial to the low background signal of the system. During the detection process, the aptamer sequence preferred to bind to kanamycin, forming aptamer-kanamycin complex. At the same time, the G-rich sequence folded into G-quadruplex structure that specifically bound to NMM under the action of K+, forming G-quadruplex/NMM complex. Under the synergistic effects of the two complexes, the integrated probe with aptamer-kanamycin complex and G-quadruplex/NMM complex was released from the graphene oxide surface due to the steric hindrance effect, restoring the strong fluorescence signal. By combining graphene oxide and G-quadruplex/NMM complex, the fluorescent biosensor could effectively achieve label-free and low-background detection of kanamycin. The linear calibration curve was in the range of 1–400 nM with a detection limit of 0.60 nM for kanamycin. It was successfully applied to analyze raw milk samples (spiked kanamycin) with recoveries of 98.33–101.25 % and also exhibited high selectivity for kanamycin. The experimental data showed that the biosensor was a potentially powerful tool for monitoring food safety.