The CO(2) adsorption characteristics of prototypical poly(ethyleneimine)/silica composite adsorbents can be drastically enhanced by altering the acid/base properties of the oxide support via incorporation of Zr into the silica support. Introduction of an optimal amount of Zr resulted in a significant improvement in the CO(2) capacity and amine efficiency under dilute (simulated flue gas) and ultradilute (simulated ambient air) conditions. Adsorption experiments combined with detailed characterization by thermogravimetric analysis, temperature-programmed desorption, and in situ FT-IR spectroscopy clearly demonstrate a stabilizing effect of amphoteric Zr sites that enhances the adsorbent capacity, regenerability, and stability over continued recycling. It is suggested that the important role of the surface properties of the oxide support in these polymer/oxide composite adsorbents has been largely overlooked and that the properties may be even further enhanced in the future by tuning the acid/base properties of the support.

The structural changes of γ-Al 2 O 3 , Ni/γ-Al 2 O 3 , and Pt/γ-Al 2 O 3 catalysts under aqueous phase reforming conditions (liquid water at 200 °C and autogenic pressure) are examined over the course of 10 h. The changes are characterized by X-ray diffraction, NMR spectroscopy, N 2 physisorption, pyridine adsorption followed by IR spectroscopy, and electron microscopy. It is demonstrated that γ-alumina is converted into a hydrated boehmite (AlOOH) phase with significantly decreased acidity and surface area. For metal-free γ-alumina, the transformation is completed within 10 h, whereas the presence of nickel and platinum particles significantly retards the formation of boehmite. In the beginning of the treatment, the surface area of γ-alumina increases, suggesting surface pitting and formation of small boehmite particles on the surface of γ-alumina. This process is followed by the formation of a compact crystalline boehmite phase. It is proposed that the metal particles affect the kinetics of this transformation by blocking specific surface hydroxyl groups that act as initial hydration sites. The transformation of γ-alumina into boehmite is accompanied by sintering of the supported metal particles.

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Silica supported amine materials are promising compositions that can be used to effectively remove CO(2) from large stationary sources, such as flue gas generated from coal-fired power plants (ca. 10 % CO(2)) and potentially from ambient air (ca. 400 ppm CO(2)). The CO(2) adsorption characteristics of prototypical poly(ethyleneimine)-silica composite adsorbents can be significantly enhanced by altering the acid/base properties of the silica support by heteroatom incorporation into the silica matrix. In this study, an array of poly(ethyleneimine)-impregnated mesoporous silica SBA-15 materials containing heteroatoms (Al, Ti, Zr, and Ce) in their silica matrices are prepared and examined in adsorption experiments under conditions simulating flue gas (10 % CO(2) in Ar) and ambient air (400 ppm CO(2) in Ar) to assess the effects of heteroatom incorporation on the CO(2) adsorption properties. The structure of the composite adsorbents, including local information concerning the state of the incorporated heteroatoms and the overall surface properties of the silicate supports, are investigated in detail to draw a relationship between the adsorbent structure and CO(2) adsorption/desorption performance. The CO(2) adsorption/desorption kinetics are assessed by thermogravimetric analysis and in situ FT-IR measurements. These combined results, coupled with data on adsorbent regenerability, demonstrate a stabilizing effect of the heteroatoms on the poly(ethyleneimine), enhancing adsorbent capacity, adsorption kinetics, regenerability, and stability of the supported aminopolymers over continued cycling. It is suggested that the CO(2) adsorption performance of silica-aminopolymer composites may be further enhanced in the future by more precisely tuning the acid/base properties of the support.

The formation of surface species from two- and three-carbon polyols on γ-Al(2)O(3) in the presence and absence of coadsorbed water is investigated. Aqueous-phase adsorption isotherms indicate that competitive adsorption between water and polyol inhibits the uptake of the polyol molecules on γ-Al(2)O(3) and that the polyol with the most hydroxyl groups, glycerol, experienced the greatest uptake. Deuterium solid echo pulse NMR measurements support the fact that glycerol strongly interacts with γ-Al(2)O(3) in the presence of physisorbed water and that ethylene glycol interacts with γ-Al(2)O(3) only after the physisorbed water has been removed. In situ high-vacuum FT-IR analysis combined with DFT simulations demonstrate that glycerol readily forms a multidentate alkoxy species through its primary hydroxyl groups with coordinatively unsaturated Al atoms of γ-Al(2)O(3) in the presence of physisorbed water. This surface species exhibits a bridging alkoxy bond from one of its primary hydroxyl groups and a strong interaction with the remaining primary hydroxyl group. FT-IR analysis of 1,3-propanediol on γ-Al(2)O(3) also demonstrates the formation of a multidentate alkoxy species in the presence of coadsorbed water. In contrast, polyols with hydroxyl groups only on the one- and two-carbon atoms, ethylene glycol, and 1,2-propanediol do not form alkoxy bonds with the γ-Al(2)O(3) surface when coadsorbed water is present. These polyols will form alkoxy bonds to γ-Al(2)O(3) when coadsorbed water is removed, and these alkoxy species are removed when water is readsorbed on the sample. The formation of strongly bound, stable multidentate alkoxy species by ethylene glycol and 1,2-propanediol on γ-Al(2)O(3) is prevented by steric limitations of vicinal alcohol groups.

The stability of a 1 wt % Pt/γ-Al 2 O 3 catalyst was tested in an ethanol/water mixture at 225°C and autogenic pressure, conditions at which it is possible to dissolve and depolymerize various kinds of lignin, and structural changes to the catalysts were studied by means of X-ray diffraction (XRD), 27 Al MAS NMR, N 2 physisorption, transmission electron microscopy (TEM), H 2 chemisorption, elemental analysis, thermogravimetric analysis-mass spectrometry (TGA-MS), and IR. In the absence of reactants the alumina support is found to transform into boehmite within 4 h, leading to a reduction in support surface area, sintering of the supported Pt nanoparticles, and a reduction of active metal surface area. Addition of aromatic oxygenates to mimic the compounds typically obtained by lignin depolymerization leads to a slower transformation of the support oxide. These compounds, however, were not able to slow down the decrease in dispersion of the Pt nanoparticles. Vanillin and guaiacol stabilize the aluminum oxide more than phenol, anisole, and benzaldehyde because of the larger number of oxygen functionalities that can interact with the alumina. Interestingly, catalyst samples treated in the presence of lignin showed almost no formation of boehmite, no reduction in support or active metal surface area, and no Pt nanoparticle sintering. Furthermore, in the absence of lignin-derived aromatic oxygenates, ethanol forms a coke-like layer on the catalyst, while oxygenates prevent this by adsorption on the support by coordination via the oxygen functionalities.

The surface species formed by glycerol on γ-Al2O3, TiO2 anatase, ZrO2, MgO, and CeO2 both in the presence and in the absence of bulk water are investigated with infrared spectroscopy. The acid–base properties of the metal oxides are characterized by pyridine and CO2 adsorption/temperature-programmed desorption. The metal oxides studied provide a distribution of strengths of Lewis acid sites as well as strengths and types of basic sites which afford insight into the role of these various sites in polyol/metal oxide surface interactions. Even in the presence of bulk water, glycerol forms a bridging alkoxy bond through a primary alcohol group to two coordinatively unsaturated metal atoms and participates in a Lewis acid/base interaction between the oxygen atom of the other primary alcohol and a coordinatively unsaturated metal atom that is also involved in the alkoxy bond. These interactions only occur with metal oxides which contain strong Lewis acid sites. A quantitative correlation between the C–O stretching frequencies of the chemisorbed groups and the electronegativity of the metal atoms is established. Glycerol experiences an additional surface interaction via a hydrogen-bonding interaction between its secondary alcohol group and a relatively weak basic surface oxygen atom. Stronger base sites are blocked by adsorbed water or CO2. In the absence of strong Lewis acid sites, in the case of MgO, hydrogen-bonding interactions between glycerol and surface hydroxyls are the dominant means of interaction.

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