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Biomedical subjects

Andrew O Simm

Publications and source records attributed to Andrew O Simm.

11 recordsLinked to original sources

Nano-electrochemical detection of hydrogen or protons using palladium nanoparticles: distinguishing surface and bulk hydrogen.

The benefits of using nanoparticle-modified electrodes are exemplified through the electrochemical detection of protons and/or hydrogen. It is shown that a palladium-nanoparticle-modified boron-doped diamond allows voltammetric information relating to the relative roles played by the surface and the bulk metal to be obtained for the proton-hydrogen system at palladium surfaces which is not accessible using palladium macroelectrodes or microelectrodes.

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AFM studies of metal deposition: instantaneous nucleation and the growth of cobalt nanoparticles on boron-doped diamond electrodes.

In situ atomic force microscopy (AFM) is used to study the growth of cobalt nuclei on a boron doped diamond electrode under potentiostatic control. The rate of growth of the nuclei at the electrode surface is monitored using AFM as a function of time at different deposition potentials. The nucleation of cobalt nuclei is found to be "instantaneous" and the growth of the nuclei is shown to be kinetically rather than diffusionally controlled over periods of tens and hundreds of seconds. At very short times (<10 seconds) the kinetics of nucleation are apparent.

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The electroanalytical detection of hydrazine: a comparison of the use of palladium nanoparticles supported on boron-doped diamond and palladium plated BDD microdisc array.

We show that both a random distribution of palladium nanoparticles supported on a BDD electrode or a palladium plated BDD microelectrode array can each provide a sensing platform for the electrocatalytic detection of hydrazine. The palladium nanoparticle modified electrode displays a sensitivity and limit of detection of 60 mA mol(-1) L and 2.6 microM respectively while the array has a sensitivity of 8 mA mol(-1) L with a detection limit of 1.8 microM. The beneficial cost implications of using palladium nano- or micro-particles in sensors compared to a palladium macroelectrode are evident. Interestingly the array of the nanoparticles shows similar sensitivity and limit of detection to the microelectrode array which probably indicates that the random distribution of the former leads to 'clumps' of nanoparticles that effectively act as microelectrodes.

Boron↗

Boron-doped diamond microdisc arrays: electrochemical characterisation and their use as a substrate for the production of microelectrode arrays of diverse metals (Ag, Au, Cu)via electrodeposition.

A novel boron-doped diamond (BDD) microelectrode array is characterised with electrochemical and atomic force microscopic techniques. The array consists of 40 micron-diameter sized BDD discs which are separated by 250 microns from their nearest neighbour in a hexagonal arrangement. The conducting discs can be electroplated to produce arrays of copper, silver or gold for analytical purposes in addition to operating as an array of BDD-microelectrodes. Proof-of-concept is shown for four separate examples; a gold plated array for arsenic detection, a copper plated array for nitrate analysis, a silver plated array for hydrogen peroxide monitoring and last, cathodic stripping voltammetry for lead at the bare BDD-array.

Arsenic↗

Cysteine methyl ester modified glassy carbon spheres for removal of toxic heavy metals from aqueous media.

Glassy carbon spherical powder (10-20 microm diameter) modified with cysteine methyl ester is found to be an inexpensive, novel material for the rapid removal of large quantities of toxic heavy metal ions such as Cd(II), Cu(II) and As(III) from aqueous media, with wide ranging potential applications such as third world drinking water filtration or environmental cleanup.

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Acoustically fabricated random microelectrode assemblies.

We report the insonation of bismuth, silver, copper and tungsten metal particles suspended in octane in the vicinity of a glassy carbon electrode. AFM and voltammetry reveal that metal particles are immobilised onto the electrode substrate. In the case of bismuth, silver and copper, the possible melting of the metal particles due to the high sonochemical conditions cannot unambiguously be ruled out. However, it is likely that the immobilisation of the metal particles occurs predominantly through mechanical attachment due to the high rates of mass transport, evidenced from the fact that tungsten can be immobilised at a glassy carbon surface which has a melting point (mp 3410 degrees C) outside the likely sonochemical conditions. The immobilised particles are found to be in electrical contact with the glassy carbon electrodes which can then act as random assemblies of microelectrodes. Proof-of-concept for use in electro-analysis is examined for the possible detection of arsenic and cadmium at a silver and bismuth random microelectrode assemblies, respectively. This approach suggests a simple generic methodology for the construction of microelectrode assemblies via abrasive attachment induced by insonation with power ultrasound.

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Hydrodynamic electrochemistry: design for a high-speed rotating disk electrode.

We report a novel gas-driven high-speed rotating disk electrode (HSRDE). The HSRDE when immersed in an aqueous solution rotates at approximately 650 Hz, generating laminar flow resulting in a diffusion layer, under steady-state conditions, of thickness approximately 2 microm. The use of high-pressure gas to drive the rotator offers significant improvement in electrical noise as compared to conventional mechanically driven devices. The electroanalytical utility of the HSRDE was exemplified by the anodic stripping voltammetry of arsenic(III) at a gold working electrode. The charge under the arsenic stripping peak was found to increase by more than 1 order of magnitude under the enhanced mass transport regime at the HSRDE in comparison to that seen under quiescent conditions.

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Novel methods for the production of silver microelectrode-arrays: their characterisation by atomic force microscopy and application to the electro-reduction of halothane.

A new method is proposed for the simple preparation of random silver micro and nano-electrode arrays. This employs acoustic streaming directed at a glassy carbon surface to "mechanically" attach particles from a suspension of metal colloidal or other small particles. The particles tend to adhere to the substrate at points of imperfection such as scratches, crevices etc. These arrays are compared with arrays formed by the electro-deposition of silver at a glassy carbon substrate, with the silver being partially stripped off, leaving a stable micro and nanoparticle array on the surface. Both surfaces are characterised using optical and atomic force microscopy. The two types of electrodes are evaluated to their analytical utility via the electrochemical reduction of halothane and their performance compared with that of a silver macroelectrode. A notable increase in sensitivity and peak current is observed.

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A comparison of different types of gold-carbon composite electrode for detection of arsenic(III).

A study has been conducted using abrasively modified basal and edge-plane graphite, carbon-paste, and carbon-epoxy electrodes to create gold-carbon composite electrodes. Using either nano or micro-sized gold particles their suitability for use in detecting arsenic(III) is assessed. It was found that gold arrays prepared from micron-sized particles gave the best performance for arsenic detection. In particular micron arrays produced in carbon-paste electrodes with an easily renewable surface work well for detection of arsenic, producing a detection limit of 5(+/-2)x10(-9) mol L(-1), with a high sensitivity of 10(+/-0.1) A mol(-1) L.

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Sonically assisted electroanalytical detection of ultratrace arsenic.

A simple portable handheld electrochemical sensor with an integrated sound source for the detection of ultratrace quantities of arsenic using square wave anodic stripping voltammetry is described. The sensor uses low-frequency sound (250 Hz) during the arsenic deposition step to enhance the sensitivity of the arsenic stripping response. It is found that under quiescent (silent) conditions a detection limit of 2.1 x 10(-7) M with a sensitivity of 0.51 M(-1) A is achievable using a 120-s accumulation period, while applying low-frequency sound using a "sonotrode" reduced this detection limit to 3.7 x 10(-9) M with an increased sensitivity of 27.2 M(-1) A. Thus, the low-frequency sonotrode is shown to increase the sensitivity by ca. 50 times while reducing the limit of detection by 2 orders of magnitude. A study of the effect of copper contamination is carried out as well as analysis in real samples; it is found that although as expected copper detrimentally effects the arsenic limit of detection, it does not rise significantly above 10(-8) M levels.

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