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  • 1995-1999  (4)
  • Voltammetry  (2)
  • Capillary electrophoresis  (1)
  • Industrial Chemistry and Chemical Engineering  (1)
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Years
  • 1995-1999  (4)
Year
  • 1
    ISSN: 1040-0397
    Keywords: Capillary electrophoresis ; Pulsed electrochemical detection ; Alditols ; Carbohydrates ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Results are presented from a systematic study of the noise (N) and peak-to-noise ratio (P/N) obtained for pulsed electrochemical detection (PED) at a gold micro-wire electrode applied to a mixture of alditols and monosaccharides separated by capillary electrophoresis (CE). The electrode potentials and time periods for oxidative cleaning and reductive reactivation of the electrode were held constant in the PED waveform at minimum allowable values and the time period for digital integration of electrode current (tint) was varied from 50 to 800 ms by 50-ms intervals. The value of N was virtually independent of tint and P/N increased approximately as a linear function of tint in the range 50-200 ms corresponding to waveform frequencies in the range 4.5-2.7 Hz. A detection limit of 9 fmol glucose was determined for a 4-nL injection using tint = 200 ms.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 8 (1996), S. 726-731 
    ISSN: 1040-0397
    Keywords: Ethylamine ; Gold ; Voltammetry ; Adsorption ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Linear scan (cyclic) voltammetry at the disk with simultaneous pulsed electrochemical detection (PED) at the ring of a rotated ring-disk electrode (RRDE) is demonstrated to be applicable for studies of the complex anodic behavior of ethylamine at gold electrodes in 0.10 M NaOH. The oxidation of ethylamine at the disk occurs during positive scans concomitantly with formation of surface oxide (Au → AuOH → AuO). However, the final oxide-covered surface (AuO) is inert for further ethylamine oxidation. Data obtained at the RRDE demonstrate that the total ethylamine signal at the disk is composed of simultaneous contributions from: oxidative desorption of ethylamine preadsorbed at the oxide-free Au surface and oxidation of ethylamine transported to the disk simultaneously with oxide formation. Based on ring-disk data, preadsorbed ethylamine is estimated to correspond to a fractional surface coverage of 0.7 ± 0.1 monolayer for 10 to 60 μM ethylamine. Of this coverage, ca. 75% corresponds to ethylamine coadsorbed reversibly with OH- and 25% to ethylamine adsorbed irreversibly by a mechanism concluded to be chemisorption.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 9 (1997), S. 273-278 
    ISSN: 1040-0397
    Keywords: Titanium ; Voltammetry ; Oxygen ; Hydrogen peroxide ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bright, freshly-polished Ti electrodes give minimal cathodic response for O2 and H2O2 in 1.0 M NaOH. However, the response is increased gradually by repeated application of a triangular waveform within the approximate potential limits of O2 response (ca. -1.5 to -0.7 V vs. SCE). This same voltammetric pretreatment applied for excessive periods results in formation of golden films on the Ti surfaces that are active for reduction of O2 and H2O2. Levich plots of cathodic current for O2 and H2O2 at rotated golden-Ti disk electrodes in 1.0 M NaOH (-1.35 V) are linear over a large range of rotational velocity (42 to 513 rad s-1), a behavior considered to be indicative of fast heterogeneous kinetics. Ring-disk data demonstrate that a small amount of H2O2 is produced throughout the potential region for O2 reduction and H2O2 is concluded to be an intermediate product in the O2-reduction mechanism. These observations are consistent with those reported previously for single-crystal TiO2 electrodes.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 475-478 
    ISSN: 0268-2605
    Keywords: organomercurials ; symmetrization ; column chromatography ; organomercury halides ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The symmetrization reaction of organomercury(II) chlorides (RHgCl) to R2Hg and HgCl2 in toluene solution under identical conditions using a basic alumina column has been studied­in order to compare the effect of the nature of the R groups on the extent of symmetrization. The efficiency of symmetrization depends markedly on the electron-withdrawing nature of­R, varying from 90-94% for R = trichlorovinyl or phenyl to 11% for R = 2,6-dimethylphenyl.© 1998 John Wiley & Sons, Ltd.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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