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Teruo Hinoue

Publications and source records attributed to Teruo Hinoue.

5 recordsLinked to original sources

Thermal modulation voltammetry with laser heating at an aqueous|nitrobenzene solution microinterface: determination of the standard entropy changes of transfer for tetraalkylammonium ions.

Thermal modulation voltammetry (TMV) with laser heating was successfully performed at an aqueous|nitrobenzene (NB) solution microinterface, by taking advantage of the fact that laser light with a wavelength of 325.0 nm is optically transparent to the aqueous solution but opaque to the NB solution. When the laser beam impinges upon the interface from the aqueous solution side, a temperature is raised around the interface through the thermal diffusion subsequent to the light-to-heat conversion following the optical absorption by the NB solution near the interface. Based on such a principle, we achieved a fluctuating temperature perturbation around the interface for TMV by periodically irradiating the interface with the laser beam. On the other hand, the fluctuating temperature perturbation has influence on currents for transfer of an ion across the interface to produce fluctuating currents synchronized with the perturbation through temperature coefficients of several variables concerning the transfer, such as the standard transfer potential and the diffusion coefficient of the ion. Consequently, TMV has the possibility of providing information about the standard entropy change of transfer corresponding to a temperature coefficient of the standard transfer potential and a temperature coefficient of the diffusion coefficient. In this work, the aqueous|NB solution interface of 30 microm in diameter was irradiated with the laser beam at 10 Hz, and the currents synchronized with the periodical irradiation were recorded as a function of the potential difference across the interface in order to construct a TM voltammogram. TM voltammograms were measured for transfer of tetramethylammonium, tetraethylammonium, tetrapropylammonium, and tetra-n-butylammonium ions from the aqueous solution to the NB solution, and the standard entropy change of transfer was determined for each ion, according to an analytical procedure based on a mathematical expression of the TM voltammogram. Comparison of the values obtained in this work with the literature values has proved that TMV with laser heating is available for the determination of the standard entropy change of transfer for an ion.

Journal Article↗

Ultraviolet laser photo-modulation voltammetry of tetraphenylborate at a liquid/liquid interface.

Photo-modulation voltammetry was applied to detecting the photolysis of tetraphenylborate (TPhB) at a water/1,2-dichloroethane (DCE) interface by using a He-Cd laser emitting a beam with a major 325-nm line and minor lines of shorter wavelengths. When the interface was irradiated from the water-phase side, a new wave appeared in the photomodulation voltammogram, suggesting that TPhB was photolyzed and the anionic product was transferred across the interface. The concentration dependence of the photocurrents was successfully explained by a theory based on the photolytic process at the interface.

Electrochemistry↗

Adsorption behavior of metal ions onto a bovine serum albumin (BSA) membrane monitored by means of an electrode-separated piezoelectric quartz crystal.

The interaction between metal ions and bovine serum albumin (BSA) was studied by using a piezoelectric quartz crystal (PQC) arranged in the electrode-separated configuration. A silanized surface of the PQC was coated with a BSA membrane via a coupling reaction with glutaraldehyde. The frequency shifts obtained from PQC coated with a BSA membrane suggested that various kinds of metal ions could be adsorbed onto the BSA membrane from aqueous solutions containing a low concentration of metal ions (2 or 10 micromol dm(-3)), only when the BSA was denatured with an alkaline solution. Anionic species of Pt(IV) and Au(III) were adsorbed onto the denatured BSA membrane from an acetic acid solution at pH 2.2, and cationic species of Cd(II), Zn(II), Co(II), Ni(II), Cu(II), and Ag(I), and cations, such as Ca2+, Ba2+, and Mg2+, were adsorbed from ammonia buffer at pH 9.5, whereas Al(III), Cr(III), Fe(III), Hg(II), and Pb(II) were hardly adsorbed. The adsorption mechanisms of these metal ions are discussed, based on the electrostatic interaction between the metal ions and the denatured BSA membrane, and complex formation between the metal ions and amino acid residues of the denatured BSA. Further, the PQC coated with a denatured BSA membrane was applied to the determination of Pt and Cd, using large frequency shifts for Pt(IV) and Cd(II).

Adsorption↗

Activation effects of a platinum electrode by laser pulse irradiation on the electro-oxidation of glucose in alkaline solution.

In order to demonstrate the activation effects of a Pt electrode by laser pulse irradiation, the electro-oxidation of glucose was tested at an activated Pt electrode by cyclic voltammetry. A fixed potential was applied to the electrode, and then the electrode was irradiated with laser pulses from a Nd:YAG laser at 20 Hz for 20 s. Activation by the laser pulse irradiation gave two remarkable effects on cyclic voltammograms from the electro-oxidation of glucose in a 0.1 mol dm(-3) NaOH solution, i.e., surface modulation and cleaning effects. Significant differences were found in the cyclic voltammograms at the activated and at the simply polished electrodes. Such differences in the oxidation waves are attributed to a crystallographic change of the electrode surface induced by a laser ablation, accompanied by laser pulse irradiation. Due to the cleaning effect, the activated Pt electrode gave a sharp oxidation wave at -0.3 V even in real samples containing various organic compounds that could foul the electrode, though the activated Pt electrode lacked selectivity to the electro-oxidation of glucose.

Alkalies↗

Potentiometric response mechanism of a poly(acrylamide)-phthalocyaninato tin(II) film coated platinum electrode in acetonitrile and N,N-dimethylacetamide.

A new sensor constructed by a platinum electrode coated with a non-plasticized poly(acrylamide) polymer (PAA) film coupled with phthalocyaninato tin(II) ([Sn(II)(pc)]) was developed. The potentiometric response behavior of this PAA-[Sn(II)(pc)] electrode for such anions as CN-, F-, Cl-, and Br- in dimethylacetamide and acetonitrile were investigated. The electrode showed a Nernstian response to CN- and F- and a quite poor response to Cl- and Br-. The mechanism of the peculiar selective response was studied by cyclic voltammetric and spectrophotometric methods. The voltammetric investigation suggested that the charge of the host compound in the sensor membrane had no effect on the potential response of the electrode. It was also found by a spectrophotometric investigation that the complexing of [Sn(II)(pc)] with CN- and F- lead to the selective response of the electrode. The motive force of the complexing was considered to be a ligand exchange of CN- or F- with molecules at the axial site of [Sn(II)(pc)] due to solvent effects to the interest anions.

Journal Article↗