<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Schuttlefield, Jennifer D.</style></author><author><style face="normal" font="default" size="100%">Zeitler, Elizabeth</style></author><author><style face="normal" font="default" size="100%">Jensen, Jan H.</style></author><author><style face="normal" font="default" size="100%">Grassian, Vicki H.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Surface Reactions of Carbon Dioxide at the Adsorbed Water-Oxide Interface.</style></title><secondary-title><style face="normal" font="default" size="100%">J. Phys. Chem. CJournal of Physical Chemistry C</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">surface reaction carbon dioxide adsorbed water oxide interface</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2007///</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">111</style></volume><pages><style face="normal" font="default" size="100%">14870 - 14880</style></pages><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">In this study, FTIR spectroscopy is used to investigate surface reactions of carbon dioxide at the adsorbed water-oxide interface.  In particular, FTIR spectra following CO2 adsorption in the presence and absence of coadsorbed water on hydroxylated nanoparticulate Fe2O3 and γ-Al2O3 at 296 K are reported.  In the absence of coadsorbed water, CO2 reacts with surface O-H groups to form adsorbed bicarbonate on the surface.  In the presence of coadsorbed water, this reaction is blocked as water hydrogen bonds to the reactive M-OH sites.  Instead, CO2 reacts with adsorbed water to yield adsorbed carbonate and protonated surface hydroxyl groups, M-OH2+, through a proposed carbonic acid intermediate.  The carbonate spectra recorded between 10 and 90% RH are nearly identical to that of carbonate adsorbed on these surfaces in the presence of the liq. water.  FTIR isotope studies show that there is extensive exchange between oxygen in adsorbed water and oxygen atoms in both adsorbed carbonate and gas-phase carbon dioxide.  On the basis of these exptl. results along with quantum chem. calcns., a mechanism is proposed for surface reactions of carbon dioxide at the adsorbed water-oxide interface. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">40</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2007:1033025(Journal)</style></notes></record></records></xml>