TY - JOUR
T1 - The effect of palladium dispersion and promoters on lactose oxidation kinetics
AU - Mäki-Arvela, Päivi
AU - Murzina, Elena V.
AU - Campo, Betiana
AU - Heikkilä, Teemu
AU - Leino, Anne Riikka
AU - Kordas, Krisztian
AU - Wolf, Dorit
AU - Tokarev, Anton V.
AU - Murzin, Dmitry Yu
N1 - Funding Information:
Acknowledgements We would like to express our gratitude to the European Union for the funding of this research with the Seventh Framework Programme (project NANOCAT). Degussa is gratefully acknowledged for the catalyst samples. This work is part of the activities at the Åbo Akademi University Process Chemistry Centre within the Finnish Centres of Excellence Programme (2000–2011) appointed by the Academy of Finland. Krisztian Kordas acknowledges the Academy of Finland for funding (120853, 124357, 128626).
Copyright:
Copyright 2010 Elsevier B.V., All rights reserved.
PY - 2010/6
Y1 - 2010/6
N2 - Lactose oxidation was investigated at 70 °C and at pH 8 using oxygen as an oxidant over a comprehensive set of commercially available mono- and multi-metallic as well as promoted Pd catalysts with active carbon, alumina and calcium carbonate as catalyst supports. An optimum cluster size of 6-10 nm resulted in the highest initial turnover frequencies. High conversion levels above 90% were achieved on Pd/C catalyst, as well as over Pd/Al 2O3 and (Pd-Pb)/CaCO3, whereas (Pd-V)/C catalyst gave only 30% conversion after 200 min. The latter catalyst was relatively inactive due to its high support acidity and profound deactivation during oxidation. Besides the main oxidation product, lactobionic acid, also, lactulose was generated as a result of lactose isomerisation under alkaline conditions. The electrochemical potentials of the catalysts were measured during lactose oxidation. The main result of these measurements was that, when the electrochemical potential of the catalyst increased very quickly, its oxidation activity was low due to metal over-oxidation. The selectivities to the desired product, lactobionic acid, were relatively high, above 80% for most of the catalysts, except for (Pd-V)/C. Furthermore, the selectivity to the lactobionic acid decreased with increasing metal dispersion, thus, indicating that the optimum metal particle sizes for producing high amounts of lactobionic acid is above 3 nm.
AB - Lactose oxidation was investigated at 70 °C and at pH 8 using oxygen as an oxidant over a comprehensive set of commercially available mono- and multi-metallic as well as promoted Pd catalysts with active carbon, alumina and calcium carbonate as catalyst supports. An optimum cluster size of 6-10 nm resulted in the highest initial turnover frequencies. High conversion levels above 90% were achieved on Pd/C catalyst, as well as over Pd/Al 2O3 and (Pd-Pb)/CaCO3, whereas (Pd-V)/C catalyst gave only 30% conversion after 200 min. The latter catalyst was relatively inactive due to its high support acidity and profound deactivation during oxidation. Besides the main oxidation product, lactobionic acid, also, lactulose was generated as a result of lactose isomerisation under alkaline conditions. The electrochemical potentials of the catalysts were measured during lactose oxidation. The main result of these measurements was that, when the electrochemical potential of the catalyst increased very quickly, its oxidation activity was low due to metal over-oxidation. The selectivities to the desired product, lactobionic acid, were relatively high, above 80% for most of the catalysts, except for (Pd-V)/C. Furthermore, the selectivity to the lactobionic acid decreased with increasing metal dispersion, thus, indicating that the optimum metal particle sizes for producing high amounts of lactobionic acid is above 3 nm.
KW - Active carbon
KW - Catalyst potential
KW - Dispersion
KW - Lactose oxidation
KW - Palladium
UR - http://www.scopus.com/inward/record.url?scp=77955848345&partnerID=8YFLogxK
U2 - 10.1007/s11164-010-0143-4
DO - 10.1007/s11164-010-0143-4
M3 - Article
AN - SCOPUS:77955848345
SN - 0922-6168
VL - 36
SP - 423
EP - 442
JO - Research on Chemical Intermediates
JF - Research on Chemical Intermediates
IS - 4
ER -