Effects of Polarization on the Extents and Kinetics of Adsorption of Ionic and Neutral Aromatic Heterocyclics Exhibiting Orientation Transitions at a Porous C Electrode

Verfasser / Beitragende:
[Brian E. Conway, Jianjun Niu]
Ort, Verlag, Jahr:
2004
Enthalten in:
Zeitschrift für Physikalische Chemie/International journal of research in physical chemistry and chemical physics, 218/6/2004(2004-06-01), 709-740
Format:
Artikel (online)
ID: 378924907
LEADER caa a22 4500
001 378924907
003 CHVBK
005 20180305123614.0
007 cr unu---uuuuu
008 161128e20040601xx s 000 0 eng
024 7 0 |a 10.1524/zpch.218.6.709.33451  |2 doi 
035 |a (NATIONALLICENCE)gruyter-10.1524/zpch.218.6.709.33451 
245 0 0 |a Effects of Polarization on the Extents and Kinetics of Adsorption of Ionic and Neutral Aromatic Heterocyclics Exhibiting Orientation Transitions at a Porous C Electrode  |h [Elektronische Daten]  |c [Brian E. Conway, Jianjun Niu] 
520 3 |a Comparative investigations of the adsorption and electrosorption of the heterocyclic compounds, pyridine, 1,4-pyrazine and 1-quinoline, and their orientation behaviours in an high specific-area C-cloth/H2O interphase, directly related to the replacement of preadsorbed and field-oriented solvent (H2O) molecules by oriented adsorbates themselves, have been carried out by means of in situ UV spectrophotometry conducted under positive or negative electric polarization at the C-cloth as an electrode. Surface charge, dipole moment of the adsorbate, polarization mode, acidity of the solution (leading to cation formation) and hydrophilic/hydrophobic properties of the adsorbed molecules in relation to the solvent (H2O vs. non-aqueous) are found to have important influences on these processes and hence govern the experimentally measurable extents and rates of their adsorption. The adsorption and orientation effects were indicated by evaluation of surface-dipole potential changes represented by Esin and Markov (EM)-type effects. Different adsorption and orientation processes amongst the three adsorbates, together with the possible rearrangement of the adsorbed molecules, were revealed by changes of the observed EM effects. The preferred adsorption/electrosorption behaviour arises by either "combined adsorption” (CAD) (i.e. combination of adsorption on open-circuit with electrosorption upon subsequent polarization) or by "alternate polarization electrosorption” (APE) (i.e. electrosorption by periodically reversed direction of polarization, between positive and negative, in one adsorption experiment). Negative-current polarization in a single transient also led to similar results for effective adsorptive removal of 1-quinoline from aqueous solution. Major differences of adsorption arise between neutral pyridine and its cation in acidic solution, including the effect of electrode polarization. 
540 |a © 2004 Oldenbourg Wissenschaftsverlag GmbH 
690 7 |a Thermodynamics & statistical physics  |2 nationallicence 
690 7 |a Laboratory techniques, experiments  |2 nationallicence 
690 7 |a Physical chemistry  |2 nationallicence 
700 1 |a Conway  |D Brian E.  |4 aut 
700 1 |a Niu  |D Jianjun  |4 aut 
773 0 |t Zeitschrift für Physikalische Chemie/International journal of research in physical chemistry and chemical physics  |d Oldenbourg Wissenschaftsverlag GmbH  |g 218/6/2004(2004-06-01), 709-740  |x 0942-9352  |q 218:6/2004<709  |1 2004  |2 218  |o zpch 
856 4 0 |u https://doi.org/10.1524/zpch.218.6.709.33451  |q text/html  |z Onlinezugriff via DOI 
908 |D 1  |a research article  |2 jats 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1524/zpch.218.6.709.33451  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Conway  |D Brian E.  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Niu  |D Jianjun  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Zeitschrift für Physikalische Chemie/International journal of research in physical chemistry and chemical physics  |d Oldenbourg Wissenschaftsverlag GmbH  |g 218/6/2004(2004-06-01), 709-740  |x 0942-9352  |q 218:6/2004<709  |1 2004  |2 218  |o zpch 
900 7 |b CC0  |u http://creativecommons.org/publicdomain/zero/1.0  |2 nationallicence 
898 |a BK010053  |b XK010053  |c XK010000 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-gruyter