Electrochemical reduced graphene oxide-poly(eriochrome black T)/gold nanoparticles modified glassy carbon electrode for simultaneous determination of ascorbic acid,dopamine and uric acid

This work reports on the preparation of electrochemically reduced graphene oxide (ERGO)-poly(eriochrome black T) (pEBT) assembled gold nanoparticles for the simultaneous determination of ascorbic acid (AA), dopamine (DA) and uric acid (UA) in PBS pH 6.0. Characterisations of the composite were carried out by scanning electron microscopy (SEM), Fourier transform infrared (FTIR), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry. As a result of the synergistic effect, the modified glassy carbon electrode (GCE) possessed an efficient electrochemical catalytic activity with a high selectivity and sensitivity in oxidising AA-DA and DA-UA as compared to the bare GCE. The peak separations of AA and DA, DA and UA were 183 mV and 150 mV, respectively. The linear response ranges for AA, DA and UA were 10–900 μM, 0.5–20 μM and 2–70 μM with detection limits of 0.53 μM, 0.009 μM and 0.046 μM (S/N = 3), respectively. The sensitivity of ERGO-pEBT/AuNPs was measured as 0.003 µA/μM, 0.164 µA/μM and 0.034 µA/μM for AA, DA, and UA, respectively. The modified electrochemical sensor was used in the determination of AA, DA, and UA in vitamin C tablets and urine sample with good recovery.     

Comparative study of graphene nanosheet- and multiwall carbon nanotube-based electrochemical sensor for the sensitive detection of cadmium

A novel nanocomposite was obtained through the controlled surface modification of graphene nanosheets (nanographene) with Nafion by ultrasonic oscillation. The composite was used as an ultrasensitive platform for the detection of cadmium ions (Cd²⁺) by differential pulse anodic stripping voltammetry (DPASV) analysis. The performance of the nanographene-based sensor was systematically compared with that of a multiwall carbon nanotube (MWCNT)-modified sensor. The results indicate that the nanographene-based sensor exhibits significant advantages over the MWCNT-based sensor in terms of repeatability, sensitivity and limit of detection (LOD). The nanographene-based sensor displayed superior analytical performance over a linear range of Cd²⁺ concentrations from 0.25 μg L⁻¹ to 5 μg L⁻¹, with a LOD of 3.5 ng L⁻¹. This sensor was also used to systematically screen for 6 types of chemicals, including sodium salts, magnesium salts and zinc salts. It was observed that the sensor could successfully differentiate cadmium ions from interferents (magnesium salts, zinc salts, etc.). The nanographene-based sensor was also demonstrated to be a promising and reliable tool for the rapid detection of cadmium existing in tap water and for the rapid on-site analysis of critical pollution levels of cadmium.     

Discrimination and simultaneous determination of hydroquinone and catechol by tunable polymerization of imidazolium-based ionic liquid on multi-walled carbon nanotube surfaces

Tunable polymerization of ionic liquid on the surfaces of multi-walled carbon nanotubes (MWCNTs) was achieved by a mild thermal-initiation-free radical reaction of 3-ethy-1-vinylimidazolium tetrafluoroborate in the presence of MWCNTs. Successful modification of polymeric ionic liquid (PIL) on MWCNTs surfaces (PIL-MWCNTs) was demonstrated by scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis and X-ray photoelectron spectroscopy. The resulting PIL-MWCNTs possessed unique features of high dispersity in aqueous solution and tunable thickness of PIL layer, due to positive imidazole groups along PIL chains and controllable ionic liquid polymerization by tuning the ratio of precursor. Based on cation-π interaction between the positive imidazole groups on PIL-MWCNTs surface and hydroquinone (HQ) or catechol (CC), excellent discrimination ability toward HQ and CC and improved simultaneous detection performance were achieved. The linear range for HQ and CC were 1.0 × 10⁻⁶ to 5.0 × 10⁻⁴ M and 1.0 × 10⁻⁶ to 4.0 × 10⁻⁴ M, respectively. The detection limit for HQ was 4.0 × 10⁻⁷ M and for CC 1.7 × 10⁻⁷ M (S/N = 3), correspondingly.     

The Cu-MOF-199/single-walled carbon nanotubes modified electrode for simultaneous determination of hydroquinone and catechol with extended linear ranges and lower detection limits

A novel electrochemical sensor based on Cu-MOF-199 [Cu-MOF-199 = Cu₃(BTC)₂ (BTC = 1,3,5-benzenetricarboxylicacid)] and SWCNTs (single-walled carbon nanotubes) was fabricated for the simultaneous determination of hydroquinone (HQ) and catechol (CT). The modification procedure was carried out through casting SWCNTs on the bare glassy carbon electrode (GCE) and followed by the electrodeposition of Cu-MOF-199 on the SWCNTs modified electrode. Cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM) were performed to characterize the electrochemical performance and surface characteristics of the as-prepared sensor. The composite electrode exhibited an excellent electrocatalytic activity with increased electrochemical signals towards the oxidation of HQ and CT, owing to the synergistic effect of SWCNTs and Cu-MOF-199. Under the optimized condition, the linear response range were from 0.1 to 1453 μmol L⁻¹ (R_HQ = 0.9999) for HQ and 0.1–1150 μmol L⁻¹ (R_CT = 0.9990) for CT. The detection limits for HQ and CT were as low as 0.08 and 0.1 μmol L⁻¹, respectively. Moreover, the modified electrode presented the good reproducibility and the excellent anti-interference performance. The analytical performance of the developed sensor for the simultaneous detection of HQ and CT had been evaluated in practical samples with satisfying results.     

Improved interfacial properties of PI composites through graphene oxide and carbon nanotubes on carbon fiber surface

Carbon nanotubes (CNTs) have been identified as excellent nanoreinforcements for carbon fiber (CF)–reinforced polymers regarding a wide range of engineering applications. The outstanding properties of CNTs, such as their large surface area, high mechanical strength, and low manufacturing cost bring them to be distinguished nanoreinforcements for carbon fiber–reinforced polymers to form multifunctional and multiscale composites. Electrophoretic deposition of graphene oxide for CNTs onto the CF surface was conducted. The presence of graphene oxide–CNTs may effectively increase both the roughness and wettability of the CF surface, resulting in an improvement to the interfacial bonding strength between the CF and the polyimide (PI).     

Toxicity of graphene oxide and multi-walled carbon nanotubes against human cells and zebrafish

Graphene possesses unique physical and chemical properties, which have inspired a wide range of potential biomedical applications. However, little is known about the adverse effects of graphene on the human body and ecological environment. The purpose of our work is to make assessment on the toxicity of graphene oxide (GO) against human cell line (human bone marrow neuroblastoma cell line and human epithelial carcinoma cell line) and zebrafish (Danio rerio) by comparing the toxic effects of GO with its sister, multi-walled carbon nanotubes (MWNTs). The results show that GO has a moderate toxicity to organisms since it can induce minor (about 20%) cell growth inhibition and slight hatching delay of zebrafish embryos at a dosage of 50 mg/L, but did not result in significant increase of apoptosis in embryo, while MWNTs exhibit acute toxicity leading to a strong inhibition of cell proliferation and serious morphological defects in developing embryos even at relatively low concentration of 25 mg/L. The distinctive toxicity of GO and MWNTs should be ascribed to the different models of interaction between nanomaterials and organisms, which arises from the different geometric structures of nanomaterials. Collectively, our work suggests that GO does actual toxicity to organisms posing potential environmental risks and the result is also shedding light on the geometrical structure-dependent toxicity of graphitic nanomaterials.     

Characterization of electrodes modified with nanocomposites of cobalt tetraaminophenoxyphthalocyanine,reduced graphene and multi-walled carbon nanotubes

Abstract

Glassy carbon electrodes or plates were modified with nanocomposites consisting of cobalt tetraaminophenoxyphthalocyanine (CoTAPhPc), reduced graphene oxide nanosheets (rGONs) and multi-walled carbon nanotubes (MWCNTs). The modified electrodes were characterized using cyclic voltammetry, scanning electrochemical microscopy (SECM) and time-of-flight-secondary ion mass spectrometer (TOF-SIMS). The electrocatalytic activity of the modified electrode was tested for detection of L-cysteine. The presence of CoTAPhPc on sequential layers of MWCNT and rGONs resulted in improved detection currents compared to CoTAPhPc alone or when MWCNT/rGONs are mixed in CoTAPhPc–MWCNT/rGONs (mix)–glassy carbon electrode (GCE). CoTAPhPc–MWCNT–GCE (without rGONS) showed higher sensitivity toward l-cysteine as compared to the probes incorporating rGONs with a catalytic rate constant of 4.62?×?10⁴ M^?1s^?1 and a detection limit of 30?nM. The presence of rGONs improved the stability of the electrode.     

Electrodeposited nitrogen-doped graphene/carbon nanotubes nanocomposite as enhancer for simultaneous and sensitive voltammetric determination of caffeine and vanillin

A nitrogen-doped graphene/carbon nanotubes (NGR–NCNTs) nanocomposite was employed into the study of the electrochemical sensor via electrodeposition for the first time. The morphology and structure of NGR–NCNTs nanocomposite were investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM), respectively. Meanwhile, the electrochemical performance of the glassy carbon electrode (GCE) modified with electrodeposited NGR–NCNTs (ENGR–NCNTs/GCE) towards caffeine (CAF) and vanillin (VAN) determination was demonstrated by cyclic voltammetry (CV) and square wave voltammetry (SWV). Under optimal condition, ENGR–NCNTs/GCE exhibited a wide linearity of 0.06–50 μM for CAF and 0.01–10 μM for VAN with detection limits of 0.02 μM and 3.3 × 10⁻³ μM, respectively. Furthermore, the application of the proposed sensor in food products was proven to be practical and reliable. The desirable results show that the ENGR–NCNTs nanocomposite has promising potential in electrocatalytic biosensor application.     

碳纳米管预处理及其在催化材料中应用

本文以碳纳米管作催化剂载体为出发点,回顾了大管径尤其是大内径碳纳米管制备,介绍了不同纯化处理工艺对碳纳米管性能的影响,综述了制备、预处理等因素对碳纳米管复合材料和碳纳米管负载型催化剂性能的影响。     

A sensor based on the carbon nanotubes-ionic liquid composite for simultaneous determination of hydroquinone and catechol

MWNTs-IL-Gel/GCE, a glassy carbon electrode modified with multiwalled carbon nanotubes (MWNTs) and ionic liquids (IL), was developed to serve as a sensor for simultaneous determination of Hydroquinone (HQ) and catechol (CC) in this paper. The modified GCE showed two well-defined redox waves for HQ and CC in both CV and DPV with a peak potential separation of ca. 0.1 V, which was large enough for simultaneous detection. The results revealed that the oxidation of HQ and CC with the enhancement of the redox peak current and the decrease of the peak-to-peak separation exhibit excellent electrocatalytic behaviors. A high sensitivity of 1.8×10(-7)M with detection limits of 6.7×10(-8)M and 6.0×10(-8)M (S/N=3) for HQ and CC were obtained. Moreover, the constants of apparent electron transfer rate of HQ and CC at MWNTs-IL-Gel/GCE were calculated as 7.402 s(-1) and 8.179 s(-1), respectively, and the adsorption quantity of HQ and CC was 1.408×10(-6) mol cm(-2) with chronocoulometry. The developed sensor can be applied to determinate directly of HQ and CC in aqueous solution.     

Preparation of cobalt-tetraphenylporphyrin/reduced graphene oxide nanocomposite and its application on hydrogen peroxide biosensor

A novel cobalt-tetraphenylporphyrin/reduced graphene oxide (CoTPP/RGO) nanocomposite was prepared by a π–π stacking interaction and characterized by ultraviolet–visible absorption spectroscopy (UV–vis), Fourier transform infrared spectroscopy (FTIR) and electrochemical impedance spectroscopy (EIS). The CoTPP/RGO nanocomposite exhibited high electrocatalytic activity both for oxidation and reduction of H₂O₂. The current response was linear to H₂O₂ concentration with the concentration range from 1.0 × 10⁻⁷ to 2.4 × 10⁻³ mol L⁻¹ (R = 0.998) at the reductive potential of −0.20 V and from 1.0 × 10⁻⁷ to 4.6 × 10⁻⁴ mol L⁻¹ (R = 0.996) at the oxidative potential of +0.50 V. The H₂O₂ biosensor showed good anti-interfering ability towards oxidative interferences at the oxidative potential of +0.50 V and good anti-interfering ability towards reductive interferences at the reductive potential of −0.20 V.     

High-performance supercapacitor based on ultralight and elastic three-dimensional carbon foam/reduced graphene/polyaniline nanocomposites

A novel supercapacitor based on ultralight and elastic three-dimensional porous melamine foam-derived macroporous carbon/reduced graphene oxide/polyaniline nanocomposites were fabricated, which showed great electrical performance and cycle performance.     

MOF-derived binary mixed carbon/metal oxide porous materials for constructing simultaneous determination of hydroquinone and catechol sensor

Journal of Solid State Electrochemistry - It is a top priority to simultaneously and accurately detect hydroquinone (HQ) and catechol (CC). Here, a new strategy for constructing simultaneous...     

Synergistic effect of functional carbon nanotubes and graphene oxide on the anti‐corrosion performance of epoxy coating

In this work, we reported the synergistic effect of functional carbon nanotubes (CNTs) and graphene oxide (GO) on the anticorrosion performance of epoxy coating. For this purpose, the GO and CNTs were firstly modified by the 3‐aminophenoxyphthalonitrile to realize the nitrile functionalized graphene oxides (GO‐CN) and carbon nanotubes (CNTs‐CN). As modified GO‐CN and CNTs‐CN were characterized and confirmed by Fourier transform infrared spectroscopy, X‐ray photoelectron spectroscopy, and gravimetric analyzer. It was found that about 19 and 24 wt% of 3‐aminophenoxyphthalonitrile were grafted onto the surface of the GO and CNTs, respectively. The electrochemical impedance spectroscopy results showed that the GO‐CN&CNTs‐CN hybrid materials exhibit a remarkable superiority in enhancing the anticorrosion performance of epoxy coatings. Significant synergistic effect of the lamellar structural GO‐CN and CNTs‐CN on the anticorrosion performance of epoxy composite coatings was designed. Besides, the epoxy coating with 1 wt% of the GO‐CN&CNTs‐CN hybrid exhibited the best anticorrosion performance, in which the impedance showed the largest one (immersion in 3.5 wt% of NaCl solution for 168 hr). Copyright © 2016 John Wiley & Sons, Ltd.     

The loading of polyoxometalates based compound on reduced graphene oxide,a composite material for electrical energy storage and tetracycline removal

A polyoxometalate based composite material (NiPW₁₂NP/FrGO) was synthesized successfully, in which the nanoparticle of a polyoxometalate compound (NiPW₁₂NP) distributes on carboxylate group functionalized reduced graphene oxide (FrGO) homogenously. There exist intensive chemical bonds between NiPW₁₂NP and FrGO, which guarantees the stability of this composite material. When employed as a cathode material, NiPW₁₂NP/FrGO exhibits high specific capacitance, remarkable rate capability and long-term stability. When the current density is 4 A g⁻¹, a specific capacitance as high as 437.6 F g⁻¹ is achieved by NiPW₁₂NP/FrGO. With NiPW₁₂NP/FrGO serving as cathode and MnO₂ acting as anode, a high performance asymmetric supercapacitor (ASC) is assembled, which possesses a high energy density of 12.96 W h·kg⁻¹ at 0.67 kW kg⁻¹. It also shows a good rate capability, when the current density increases from 4 to 12 A g⁻¹, its specific capacitances decreases from 115.2 to 90.9 F g⁻¹, with 78.9% capacitance retention. After 5000 cycles charge-discharge experiments, 94.3% of its capacitance can be maintained, which exhibits good stability. Furthermore, NiPW₁₂NP/FrGO composite material also shows excellent tetracycline adsorption ability with capacity 288.28 mg g⁻¹, the adsorption can be well described with Temkin model, which suggests electrostatic attraction dominates the adsorption process.     

在3,4-二羟基肉桂酸介质中以多壁碳纳米管为传感器电催化检测L-半胱氨酸(英文)

A highly sensitive electrochemical sensor was prepared for the determination of L-cysteine using a modified multiwall carbon nanotubes paste electrode in the presence of 3,4-dihydroxycinnamic acid(3,4-DHCA) as a mediator, based on an electrocatalytic process. The results indicate that the electrode is electrocatalytically efficient for the oxidation of L-cysteine in the presence of 3,4-DHCA. The interaction between the mediator and L-cysteine can be used for its sensitive and selective determination. Using chronoamperometry, the catalytic reaction rate constant was calculated to be 2.37 × 102 mol–1 L s–1. The catalytic peak current was linearly dependent on the L-cysteine concentration in the range of 0.4–115 μmol/L. The detection limit obtained by linear sweep voltammetry was 0.25 μmol/L. Finally, the modified electrode was examined as a selective, simple, and precise new electrochemical sensor for the determination of L-cysteine in real samples.     

Influence of micelles on the electrochemical behaviors of catechol and hydroquinone and their simultaneous determination

A simple and highly selective electrochemical method for the simultaneous determination of CAT and HQ at a glassy carbon electrode in micellar solutions has been developed. The electrochemical behaviors of CAT and HQ in aqueous CPB and SDBS micellar solutions have been studied by cyclic voltammetry. The oxidation peak potentials shift negatively, the reduction peak potentials shift positively, and the peak currents increase in the presence of CPB for both CAT and HQ. However, the oxidation peak potentials shift positively, the reduction peak potentials shift negatively, and the peak currents decrease in the presence of SDBS for both CAT and HQ. The electrochemical kinetic parameters for CAT and HQ in aqueous CPB and SDBS micellar solutions were also determined by chronocoulometry (CC) and chronoamperometry (CA). The cyclic and pulse differential voltammetric behaviors of the system consisting of CAT coexisting with HQ were also investigated in this work. It was found that the oxidation peak potential waves of CAT and HQ were separated by 100 mV in the presence of CPB in 0.10 M PBS (pH 6.8). Therefore, CAT and HQ can be determined simultaneously in such a system. This simple method was applied to the simultaneous determination of HQ and CAT in a household tap water sample and it exhibited high selectivity.     

还原氧化石墨烯/碳纳米管/Co_3O_4三元复合材料的制备与电化学性能

将低温水热反应和低温热处理相结合,制备了含还原氧化石墨烯(RGO)、碳纳米管(CNTs)和Co3O4的三元纳米复合材料RGO-CNTs-Co3O4;利用X射线衍射仪、扫描电子显微镜、透射电子显微镜分析了合成产物的相组成和微观结构,分析了其形成过程;并利用电化学测试装置测定了其作为锂离子电池负极材料的电化学性能.结果表明,在合成反应过程中,氧化石墨烯被还原剂肼还原为石墨烯,同时在石墨烯和CNTs表面生成氢氧化钴;再经低温热处理得到RGO-CNTs-Co3O4三元复合材料.Co3O4纳米颗粒均匀分散在由RGO片层和CNTs组成的三维网络结构中;这种三维网络结构既有利于电子和离子的传输,又能够有效抑制Co3O4在脱嵌锂过程中因体积变化引起的结构破坏.总体而言,合成的新型三元复合材料具有高的比容量以及良好的循环性能与倍率性能.     

Multilayer films of carbon nanotubes and redox polymer on screen-printed carbon electrodes for electrocatalysis of ascorbic acid

Multilayer films containing multiwall carbon nanotubes and redox polymer were successfully fabricated on a screen-printed carbon electrode using layer-by-layer (LBL) assembled method. UV-vis spectroscopy, X-ray photoelectron spectroscopy, field-emission scanning electron microscopy and electrochemical method were used to characterize the assembled multilayer films. The multilayer films modified electrodes exhibited good electrocatalytic activity towards the oxidation of ascorbic acid (AA). Compared with the bare electrode, the oxidation peak potential negatively shifted about 350 mV (versus Ag/AgCl). Furthermore, the modified screen-printed carbon electrodes (SPCEs) could be used for the determination of ascorbic acid in real samples.     

A review on the mechanical,electrical and EMI shielding properties of carbon nanotubes and graphene reinforced polycarbonate nanocomposites

Recently, it has been found that carbon nanotubes (CNTs) and graphene could prove to be the most promising carbonaceous fillers in polymers nanocomposites field because of their better structural and functional properties. Their uniform dispersion in polymer matrix leads to significant improvements in their several properties. This paper reviews the effect of nanofillers, ie, CNTs, derivatized CNTs, and graphene on the polycarbonate nanocomposite and its application in aerospace, automobile, sports, electronic sectors, and various industries. The comparative analysis of carbon‐based fillers on the different properties of polycarbonate nanocomposites is also included.