Microwave-enhanced electro-deposition and stripping of palladium at boron-doped diamond electrodes
In situ microwave activation has been applied to the electro-deposition and stripping of palladium metal (which is widely used as a catalyst) at cavitation resistant boron-doped diamond electrodes. Focused microwave radiation leading to heating, boiling, and cavitation is explored as an option to im...
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Published in | Talanta (Oxford) Vol. 72; no. 1; pp. 66 - 71 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
15.04.2007
Oxford Elsevier |
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Abstract | In situ microwave activation has been applied to the electro-deposition and stripping of palladium metal (which is widely used as a catalyst) at cavitation resistant boron-doped diamond electrodes. Focused microwave radiation leading to heating, boiling, and cavitation is explored as an option to improve the speed and sensitivity of the analytical detection procedure. The deposition and anodic stripping of palladium by linear sweep voltammetry in 0.1
M KCl (pH 2) solution and at boron-doped diamond electrodes is shown to be strongly enhanced by microwave activation due to both (i) the increase in mass transport and (ii) the increase in the kinetic rate of deposition and stripping.
The temperature at the electrode surface is calibrated with the reversible redox couple Fe(CN)
6
4−/Fe(CN)
6
3− and found to be reach 380
K. In the presence of microwave radiation, the potential of onset of the deposition of palladium is strongly shifted positive from −0.4 to +0.1
V versus SCE. The optimum potential for deposition in the presence of microwaves is −0.4
V versus SCE and the anodic stripping peak current is shown to increase linearly with deposition time. Under these conditions, the stripping peak current varies linearly with the palladium concentration down to ca. 2
μM. At concentration lower than this a logarithmic variation of the stripping peak current with concentration is observed down to ca. 0.1
μM (for 5
min pre-concentration in presence of microwave radiation). |
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AbstractList | In situ microwave activation has been applied to the electro-deposition and stripping of palladium metal (which is widely used as a catalyst) at cavitation resistant boron-doped diamond electrodes. Focused microwave radiation leading to heating, boiling, and cavitation is explored as an option to improve the speed and sensitivity of the analytical detection procedure. The deposition and anodic stripping of palladium by linear sweep voltammetry in 0.1M KCl (pH 2) solution and at boron-doped diamond electrodes is shown to be strongly enhanced by microwave activation due to both (i) the increase in mass transport and (ii) the increase in the kinetic rate of deposition and stripping. The temperature at the electrode surface is calibrated with the reversible redox couple Fe(CN)(6)(4-)/Fe(CN)(6)(3-) and found to be reach 380K. In the presence of microwave radiation, the potential of onset of the deposition of palladium is strongly shifted positive from -0.4 to +0.1V versus SCE. The optimum potential for deposition in the presence of microwaves is -0.4V versus SCE and the anodic stripping peak current is shown to increase linearly with deposition time. Under these conditions, the stripping peak current varies linearly with the palladium concentration down to ca. 2muM. At concentration lower than this a logarithmic variation of the stripping peak current with concentration is observed down to ca. 0.1muM (for 5min pre-concentration in presence of microwave radiation). In situ microwave activation has been applied to the electro-deposition and stripping of palladium metal (which is widely used as a catalyst) at cavitation resistant boron-doped diamond electrodes. Focused microwave radiation leading to heating, boiling, and cavitation is explored as an option to improve the speed and sensitivity of the analytical detection procedure. The deposition and anodic stripping of palladium by linear sweep voltammetry in 0.1 M KCl (pH 2) solution and at boron-doped diamond electrodes is shown to be strongly enhanced by microwave activation due to both (i) the increase in mass transport and (ii) the increase in the kinetic rate of deposition and stripping. The temperature at the electrode surface is calibrated with the reversible redox couple Fe(CN) 6 4−/Fe(CN) 6 3− and found to be reach 380 K. In the presence of microwave radiation, the potential of onset of the deposition of palladium is strongly shifted positive from −0.4 to +0.1 V versus SCE. The optimum potential for deposition in the presence of microwaves is −0.4 V versus SCE and the anodic stripping peak current is shown to increase linearly with deposition time. Under these conditions, the stripping peak current varies linearly with the palladium concentration down to ca. 2 μM. At concentration lower than this a logarithmic variation of the stripping peak current with concentration is observed down to ca. 0.1 μM (for 5 min pre-concentration in presence of microwave radiation). |
Author | Marken, Frank Hanson, Harriet Ghanem, Mohamed A. Coles, Barry A. Compton, Richard G. |
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Keywords | Linear sweep voltammetry Stripping Boron-doped diamond Microwave Palladium Deposition Sensor Catalytic reaction In situ Anodic stripping voltammetry Carbon electrode Diamond Metal Chemical sensor Chemical enrichment Boron Chemical modification Sensitivity Redox couple Catalyst |
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References | Gründler, Degenring (bib4) 2001; 512 Marken, Tsai, Matthews, Compton (bib8) 2000; 24 Tsai, Coles, Holt, Foord, Marken, Compton (bib29) 2001; 13 Marken, Matthews, Compton, Coles (bib10) 2000; 12 Ghanem, Compton, Coles, Canals, Marken (bib15) 2005; 130 Zimmermann, Sures (bib20) 2004; 11 Korbut, Buckova, Tarapcik, Labuda, Gründler (bib5) 2001; 506 Ghanem, Marken, Coles, Compton (bib17) 2005; 9 Holt, Del Campo, Foord, Compton, Marken (bib26) 2001; 513 Locatelli (bib18) 2005; 17 Flechsig, Korbut, Hocevar, Thongngamdee, Ogorevc, Gründler, Wang (bib6) 2002; 14 Compton, Coles, Marken (bib9) 1998 Marken, Tsai, Saterlay, Coles, Tibbetts, Holt, Goeting, Foord, Compton (bib30) 2001; 5 Tsai, Coles, Compton, Marken (bib27) 2001; 13 Coles, Moorcroft, Compton (bib3) 2001; 513 Qiu, Compton, Marken, Wilkins, Goeting, Foord (bib1) 2000; 72 Marken, Sur, Coles, Compton (bib31) 2006; 51 Richens (bib33) 1997 Tsai, Coles, Compton, Marken (bib13) 2002; 124 Zhang, Wang, Qu (bib22) 1984; 1 Batchelor-McAuley, Banks, Simm, Jones, Compton (bib34) 2006; 131 Sur, Marken, Compton, Coles (bib12) 2004; 28 The asymmetry observed for anodic, and cathodic limiting currents observed at boron-doped diamond under microwave conditions is unexplained (see Fig. 1A) and not observed at platinum electrodes. The effect occurs for several redox systems and remains to be further investigated. Palacios, Gomez, Moldovan, Morrison, Rauch, McLeod, Ma, Laserna, Lucena, Caroli, Alimonti, Petrucci, Bocca, Schramel, Lustig, Zischka, Wass, Stenbom, Luna, Saenz, Santamaria (bib21) 2000; 257 Sur, Marken, Coles, Compton, Dupont (bib14) 2004 Sur, Marken, Rees, Coles, Compton, Seager (bib11) 2004; 573 Flechsig, Korbut, Gründler (bib7) 2001; 13 Compton, Foord, Marken (bib25) 2003; 15 Baranski (bib2) 2002; 74 Sures, Zimmermann, Messerschmidt, Von Bohlen (bib19) 2002; 11 Locatelli (bib23) 2006; 557 Sur, Marken, Coles, Compton (bib28) 2004; 28 Sur, Marken, Seager, Foord, Chatterjee, Coles, Compton (bib16) 2005; 17 Wang (bib24) 1985 |
References_xml | – volume: 513 start-page: 94 year: 2001 ident: bib26 publication-title: J. Electroanal. Chem. contributor: fullname: Marken – year: 1997 ident: bib33 article-title: The Chemistry of Aqua Ions contributor: fullname: Richens – volume: 5 start-page: 313 year: 2001 ident: bib30 publication-title: J. Solid State Electrochem. contributor: fullname: Compton – volume: 11 start-page: 194 year: 2004 ident: bib20 publication-title: Environ. Sci. Poll. Res. contributor: fullname: Sures – volume: 512 start-page: 74 year: 2001 ident: bib4 publication-title: J. Electroanal. Chem. contributor: fullname: Degenring – volume: 124 start-page: 9784 year: 2002 ident: bib13 publication-title: J. Am. Chem. Soc. contributor: fullname: Marken – volume: 9 start-page: 809 year: 2005 ident: bib17 publication-title: J. Solid State Electrochem. contributor: fullname: Compton – volume: 72 start-page: 2362 year: 2000 ident: bib1 publication-title: Anal. Chem. contributor: fullname: Foord – start-page: 2816 year: 2004 ident: bib14 publication-title: Chem. Commun. contributor: fullname: Dupont – volume: 17 start-page: 385 year: 2005 ident: bib16 publication-title: Electroanalysis contributor: fullname: Compton – volume: 74 start-page: 1294 year: 2002 ident: bib2 publication-title: Anal. Chem. contributor: fullname: Baranski – volume: 28 start-page: 1544 year: 2004 ident: bib28 publication-title: New J. Chem. contributor: fullname: Compton – volume: 513 start-page: 87 year: 2001 ident: bib3 publication-title: J. Electroanal. Chem. contributor: fullname: Compton – volume: 130 start-page: 1425 year: 2005 ident: bib15 publication-title: Analyst contributor: fullname: Marken – volume: 257 start-page: 1 year: 2000 ident: bib21 publication-title: Sci. Total Environ. contributor: fullname: Santamaria – volume: 506 start-page: 143 year: 2001 ident: bib5 publication-title: J. Electroanal. Chem. contributor: fullname: Gründler – volume: 573 start-page: 175 year: 2004 ident: bib11 publication-title: J. Electroanal. Chem. contributor: fullname: Seager – volume: 17 start-page: 140 year: 2005 ident: bib18 publication-title: Electroanalysis contributor: fullname: Locatelli – volume: 51 start-page: 2195 year: 2006 ident: bib31 publication-title: Electrochim. Acta contributor: fullname: Compton – volume: 13 start-page: 831 year: 2001 ident: bib29 publication-title: Electroanalysis contributor: fullname: Compton – volume: 15 start-page: 1349 year: 2003 ident: bib25 publication-title: Electroanalysis contributor: fullname: Marken – volume: 13 start-page: 639 year: 2001 ident: bib27 publication-title: Electroanalysis contributor: fullname: Marken – volume: 24 start-page: 653 year: 2000 ident: bib8 publication-title: New J. Chem. contributor: fullname: Compton – start-page: 2595 year: 1998 ident: bib9 publication-title: Chem. Commun. contributor: fullname: Marken – volume: 557 start-page: 70 year: 2006 ident: bib23 publication-title: Anal. Chim. Acta contributor: fullname: Locatelli – volume: 28 start-page: 1544 year: 2004 ident: bib12 publication-title: New J. Chem. contributor: fullname: Coles – volume: 12 start-page: 267 year: 2000 ident: bib10 publication-title: Electroanalysis contributor: fullname: Coles – volume: 13 start-page: 786 year: 2001 ident: bib7 publication-title: Electroanalysis contributor: fullname: Gründler – year: 1985 ident: bib24 article-title: Stripping Analysis: Principal, Instrumentation and Application contributor: fullname: Wang – volume: 11 start-page: 385 year: 2002 ident: bib19 publication-title: Ecotoxicology contributor: fullname: Von Bohlen – volume: 14 start-page: 192 year: 2002 ident: bib6 publication-title: Electroanalysis contributor: fullname: Wang – volume: 1 start-page: 291 year: 1984 ident: bib22 publication-title: Mikrochim. Acta contributor: fullname: Qu – volume: 131 start-page: 106 year: 2006 ident: bib34 publication-title: Analyst contributor: fullname: Compton |
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Snippet | In situ microwave activation has been applied to the electro-deposition and stripping of palladium metal (which is widely used as a catalyst) at cavitation... |
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SubjectTerms | Analytical chemistry Boron-doped diamond Chemistry Deposition Electrochemical methods Exact sciences and technology General, instrumentation Linear sweep voltammetry Microwave Palladium Sensor Stripping |
Title | Microwave-enhanced electro-deposition and stripping of palladium at boron-doped diamond electrodes |
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