Gas phase oxidation as a tool to introduce oxygen containing groups on metal-loaded carbon nanofibers

Oxygen containing groups were introduced, onto carbon nanofibers (CNFs) that were previously loaded with palladium, using HNO3 vapor. Using traditional liquid-phase oxidations this is not possible due to severe metal leaching. For the samples oxidized using HNO3 vapor temperature programmed desorption and X-ray photoelectron spectroscopy revealed the presence of two major classes of oxygen containing groups, i.e. carboxylic acid groups which are thermally stable up to 300 °C and less acidic (e.g. phenol) and basic groups which were stable up to 700 °C. The amount of acidic oxygen containing groups introduced by this gas-phase treatment ranged from 0.1 to 0.3 mmol/g, as determined by titration. The latter amount is comparable to that introduced by traditional liquid-phase treatment in 65% HNO3 on bare CNFs. Transmission electron microscopy and H2-chemisorption measurements show a gradual increase of the average metal particle size from 2.1 nm for the starting Pd/CNF to 4.5 nm for Pd/CNF treated for 75 h in HNO3 vapor indicating that the extent of sintering with gas-phase treatment is limited. Elemental analysis showed that no leaching occurred upon gas-phase oxidation, whereas 90% of the metal was lost with a liquid-phase reflux HNO3 treatment.

[1]  T. A. Nijhuis,et al.  Support effects in hydrogenation of cinnamaldehyde over carbon nanofiber-supported platinum catalysts: Kinetic modeling , 2005 .

[2]  M. Muhler,et al.  Microkinetic modeling of CO TPD spectra using coverage dependent microcalorimetric heats of adsorption. , 2006, Physical chemistry chemical physics : PCCP.

[3]  M Brun,et al.  XPS, AES and Auger parameter of Pd and PdO , 1999 .

[4]  José L. Figueiredo,et al.  The effects of different activated carbon supports and support modifications on the properties of Pt/AC catalysts , 2001 .

[5]  K. P. Jong,et al.  Preparation of Carbon‐Supported Metal Catalysts , 2008 .

[6]  H. Toghiani,et al.  Nitric acid oxidation of vapor grown carbon nanofibers , 2004 .

[7]  Jiango Li,et al.  Surface functionalization and characterization of graphitic carbon nanofibers (GCNFs) , 2005 .

[8]  Wei Xia,et al.  Thermal Stability and Reducibility of Oxygen-Containing Functional Groups on Multiwalled Carbon Nanotube Surfaces: A Quantitative High-Resolution XPS and TPD/TPR Study , 2008 .

[9]  K. P. Jong,et al.  Preparation of carbon nanofiber supported platinum and ruthenium catalysts: Comparison of ion adsorption and homogeneous deposition precipitation , 2004 .

[10]  D. Su,et al.  On the Nature of Oxygen-Containing Surface Groups on Carbon Nanofibers and Their Role for Platinum Deposition―An XPS and Titration Study , 2009 .

[11]  A. Pijpers,et al.  Surface Characterization of Supported and Nonsupported Hydrogenation Catalysts , 1985 .

[12]  D. C. Koningsberger,et al.  Surface oxidation of carbon nanofibres. , 2002, Chemistry.

[13]  T. Bandosz Surface Chemistry of Carbon Materials , 2008 .

[14]  P. Serp,et al.  MWCNT activation and its influence on the catalytic performance of Pt/MWCNT catalysts for selective hydrogenation , 2008 .

[15]  A. Falqui,et al.  Influence of particles alloying on the performances of Pt–Ru/CNT catalysts for selective hydrogenation , 2011 .

[16]  W. Gac,et al.  Reduction and oxidation of a Pd/activated carbon catalyst: evaluation of effects , 2010 .

[17]  F. Xiao,et al.  High Activity in Catalytic Oxidation of Benzyl Alcohol with Molecular Oxygen over Carboxylic-Functionalized Carbon Nanofiber-Supported Ruthenium Catalysts , 2009 .

[18]  T. A. Nijhuis,et al.  Support effects in the hydrogenation of cinnamaldehyde over carbon nanofiber-supported platinum catalysts: characterization and catalysis , 2004 .

[19]  E. Teller,et al.  ADSORPTION OF GASES IN MULTIMOLECULAR LAYERS , 1938 .

[20]  K. P. Jong,et al.  The influence of oxidation on the texture and the number of oxygen-containing surface groups of carbon nanofibers , 2004 .

[21]  De Chen,et al.  Role of surface oxygen in the preparation and deactivation of carbon nanofiber supported cobalt Fischer–Tropsch catalysts , 2007 .

[22]  J. Bitter,et al.  On the origin of the cobalt particle size effects in Fischer-Tropsch catalysis. , 2009, Journal of the American Chemical Society.

[23]  L. Pfefferle,et al.  Effect of surface oxygen containing groups on the catalytic activity of multi-walled carbon nanotube supported Pt catalyst , 2010 .

[24]  E. Borguet,et al.  Detecting and quantifying oxygen functional groups on graphite nanofibers by fluorescence labeling of surface species , 2010 .

[25]  De Chen,et al.  Carbon nanofiber-supported palladium nanoparticles as potential recyclable catalysts for the Heck reaction , 2009 .

[26]  E. V. Ramos‐Fernández,et al.  Effect of thermal treatments on the surface chemistry of oxidized activated carbons , 2007 .

[27]  M. Seah,et al.  Practical Surface Analysis , 1992 .

[28]  K. D. de Jong,et al.  Carbon Nanofibers: Catalytic Synthesis and Applications , 2000 .

[29]  J. Bitter,et al.  Nanostructured carbons in catalysis a Janus material—industrial applicability and fundamental insights , 2010 .

[30]  K. J. Hüttinger,et al.  Surface-oxidized carbon fibers: I. Surface structure and chemistry , 1996 .

[31]  J. Yates,et al.  Etching of carbon nanotubes by ozone--a surface area study. , 2005, Langmuir : the ACS journal of surfaces and colloids.

[32]  G. Somorjai,et al.  TPD and XPS studies of O2, CO2, and H2O adsorption on clean polycrystalline graphite , 1988, Carbon.

[33]  J. Figueiredo,et al.  Modification of the surface chemistry of activated carbons , 1999 .

[34]  D. Su,et al.  Oxidation Stability of Multiwalled Carbon Nanotubes for Catalytic Applications , 2010 .

[35]  C. Jin,et al.  A highly efficient gas-phase route for the oxygen functionalization of carbon nanotubes based on nitric acid vapor , 2009 .

[36]  Freek Kapteijn,et al.  Cobalt particle size effects in the Fischer-Tropsch reaction studied with carbon nanofiber supported catalysts. , 2006, Journal of the American Chemical Society.