Facile and One Pot Synthesis of Gold Nanoparticles Using Tetraphenylborate and Polyvinylpyrrolidone for Selective Colorimetric Detection of Mercury Ions in Aqueous Medium

In this work, we reported for the first time, a facile and one step synthesis of gold nanoparticles from HAuCl4, employing tetraphenylborate as the reducing agent. The synthesis is not only facile but also yields “dumb-bell-shaped”particles. This shape appears to arise from a possible emulsion of the products of oxidation/decomposition of tetraphenylborate by HAuCl4, surrounding the particle. The size and shape of the AuNPs were characterized by Transmission electron microscopy (TEM) and UV-visible Spectroscopy. Interestingly, the addition of polyvinylpyrrolidone (PVP) during the synthesis was found to enhance the stability of the nanoparticle dispersion. The particles synthesized under these conditions assume “spherical” shape with the appearance of only transverse surface plasmon resonance band. The highlight of the observations is that the gold nanoparticles synthesized using tetraphenylborate as reducing agent and PVP as stabilizer are highly stable in alkaline medium, in contrast to the synthesis wherein borohydride is used as reducing agent. The AuNPs synthesized using tetraphenylborate and PVP show their mercury sensing behavior only in the alkaline medium. The color of the nanoparticle dispersion undergoes distinct color change from pink to blue with the addition of mercury ions. They also show dramatic selectivity to mercury ions in presence of other interfering ions, Pb2+, Zn2+ and Ca2+

Nano-cement composite with graphene oxide produced from epigenetic graphite deposit

This study presents the development of a nano-cement composite with graphene oxide (GO) carbon-based nanomaterials synthesized from a high-purity epigenetic graphite deposit. Diamond drill sampled graphite mineralization was upgraded through beneficiation and purification to recover a high-purity graphite product (99.9% graphitic carbon “Cg”). An alternate and improved chemical oxidation process based on the Modified Hummers method was adopted for the synthesis of GO from high-purity graphite. Microstructural analysis were performed to characterise GO. The GO consists of single bondOH, single bondC=O, single bondCOOH, and C-O-C functional groups with a layer thickness of 1.2 nm, 2 to 3 layers of graphene, an interlayer distance of 0.90 nm and a Raman (ID/IG) ratio of 0.79. The effect of 0.02, 0.04, and 0.06 wt% GO of cement on the composite workability, hydration, microstructure, mechanical and transport properties was determined. Increasing the concentration of GO in the composite decreased the workability due to the hydrophilic nature of the 2D planar surface. The rate of hydration accelerated and the cumulative hydration heat increased with the increasing proportions of GO in the composite. GO dosages about 0.02 and 0.04 wt% of cement in the composites resulted the maximum enhancement of compressive and flexural strength by 83 and 26%, respectively, compared to the control mix (0 wt% GO). The microstructural investigation shows that GO enhanced the hydration of calcium hydroxide (CH) and calcium silicate hydrate (C-S-H) during the nucleation and growth stages, filled pores, bridged micro-cracks and created interlocking between the cement hydration products. Collectively, these effects ultimately improved the mechanical properties of the composites. Also, in this process, the 0.02 and 0.04 wt% GO cement composite increased the electrical resistivity by 11.5%, and decreased the sorptivity by 29%, respectively, both of which improved the overall performance of the composite

Sensitive Electrochemical Detection of Caffeic Acid in Wine Based on Fluorine-Doped Graphene Oxide

We report here a novel electrochemical sensor developed using fluorine-doped graphene oxide (F-GO) for the detection of caffeic acid (CA). The synthesized graphene oxide (GO) and F-GO nanomaterials were systematically characterized with a scanning electron microscope (SEM), and the presence of semi-ionic bonds was confirmed in the F-GO using X-ray photoelectron spectroscopy. The electrochemical behaviours of bare glassy carbon electrode (GCE), F-GO/GCE, and GO/GCE toward the oxidation of CA were studied using cyclic voltammetry (CV), and the results obtained from the CV investigation revealed that F-GO/GCE exhibited the highest electrochemically active surface area and electrocatalytic activity in contrast to the other electrodes. Differential pulse voltammetry (DPV) was employed for the analytical quantitation of CA, and the F-GO/GCE produced a stable oxidation signal over the selected CA concentration range (0.5 to 100.0 μM) with a low limit of detection of 0.018 μM. Furthermore, the acquired results from the selectivity studies revealed a strong anti-interference capability of the F-GO/GCE in the presence of other hydroxycinnamic acids and ascorbic acid. Moreover, the F-GO/GCE offered a good sensitivity, long-term stability, and an excellent reproducibility. The practical application of the electrochemical F-GO sensor was verified using various brands of commercially available wine. The developed electrochemical sensor successfully displayed its ability to directly detect CA in wine samples without pretreatment, making it a promising candidate for food and beverage quality control

Electrochemical behavior of gold-silver alloy nanoparticles

We report the voltammetry of alloy nanoparticles via the cyclic voltammetry of gold-silver alloy nanoparticles. Through careful comparison with the response of pure gold nanoparticles, pure silver nanoparticles and their mixture the contrasting electrochemical behavior of the alloy nanoparticles is established, providing insights into the electrochemical stability of gold-silver alloy nanoparticles in chloride-containing media

Electrochemical behavior of gold-silver alloy nanoparticles

We report the voltammetry of alloy nanoparticles via the cyclic voltammetry of gold-silver alloy nanoparticles. Through careful comparison with the response of pure gold nanoparticles, pure silver nanoparticles and their mixture the contrasting electrochemical behavior of the alloy nanoparticles is established, providing insights into the electrochemical stability of gold-silver alloy nanoparticles in chloride-containing media