Mixed metal oxides, adsorption

Catalyst characterization - Characterization of mixed metal oxides was performed by atomic emission spectroscopy with inductively coupled plasma atomisation (ICP-AES) on a CE Instraments Sorptomatic 1990. NH3-TPD was nsed for the characterization of acid site distribntion. SZ (0.3 g) was heated up to 600°C using He (30 ml min ) to remove adsorbed components. Then, the sample was cooled at room temperatnre and satnrated for 2 h with 100 ml min of 8200 ppm NH3 in He as carrier gas. Snbseqnently, the system was flashed with He at a flowrate of 30 ml min for 2 h. The temperatnre was ramped np to 600°C at a rate of 10°C min. A TCD was used to measure the NH3 desorption profile. Textural properties were established from the N2 adsorption isotherm. Snrface area was calcnlated nsing the BET equation and the pore size was calcnlated nsing the BJH method. The resnlts given in Table 33.4 are in good agreement with varions literature data. 

G.M. Medine et al., Synthesis and adsorption properties of intimately intermingled mixed metal oxide nanoparticles. J. Mater. Chem. 14, 757-763 (2004)... 

Results with intimately mixed oxides show that further enhancement of reactivity for these detoxification reactions can be achieved. Mixed metal oxide systems of AP-Mg0-Al203 and AP-Ca0-Al203 are better at destructively adsorbing paraoxon than AP-MgO, AP-CaO and AP-A1203 by themselves.10 Sulfated mixed metal oxides also show further improved adsorption suggesting that increasing the acidity of the sample enhances adsorption.10... 

Mo-V-Te and Mo-V-Te-Nb mixed-metal oxide catalysts have been characterized by means of C3H8-TPR and NH3 adsorption calorimetry. All samples were strongly heterogeneous, with initial adsorption heats of = 100-80 kJ moT for the Mo-V-Te samples. Introducing an Nb component into the catalysts slightly decreased the initial adsorption heats to = 60 kJ moT but drastically increased the surface density of weak acid sites (<30kJ moT ) [83]. 

In most recent calorimetric studies of the acid-base properties of metal oxides or mixed metal oxides, ammonia and n-butylamine have been used as the basic molecule to characterize the surface acidity, with a few studies using pyridine, triethylamine, or another basic molecule as the probe molecule. In some studies, an acidic probe molecule like CO2 or hexafluoroisopropanol have been used to characterize the surface basicity of metal oxides. A summary of these results on different metal oxides will be presented throughout this article. Heats of adsorption of the basic gases have been frequently measured near room temperature (e.g., 35, 73-75, 77, 78,81,139-145). As demonstrated in Section 111, A the measurement of heats of adsorption of these bases at room temperature might not give accurate quantitative results owing to nonspecific adsorption. 

The acid-base properties of amorphous mixed metal oxides can be varied by choosing different metal oxide constituents at diflerent concentrations and by changing the treatment of the sample (44). Thus, it appears that, by properly choosing the aforementioned variables, mixed oxides could be used to develop new catalysts with desired acid-base properties. The use of micro-calorimetric adsorption measurements to quantify the acid-base properties of metal oxides and mixed metal oxides has been limited, to date, to a few systems. However, for some of these solids, for example, silica, alumina, and silica-alumina, several investigations have led to a satisfactory description of their acidity and acid strength. We present here a compendium of those measurements and discuss some of the important properties observed. 

Polychronopoulou, K., Fierro, J.L.G., and Efstathiou, A.M. Novel Zn-Ti-based mixed metal oxides for low-temperature adsorption of H2S from industrial gas streams. Applied Catalysis. B, Environmental, 2005, 57, 125. 

The perovskite-type catalysts (ref.l), other non noble metal complex oxides catalysts (ref.2), and mixed metal oxides catalysts (ref.3) have been studied in our laboratory. The various preparation techniques of catalysts (ref.4 and 5), the adsorption and thermal desorption of CO, C2H5 and O2 (ref.6 and 7), the reactivity of lattice oxygen (ref.8), the electric conductance of catalysts (ref.9), the pattern of poisoning by SO2 (ref. 10 and 11), the improvement of crushing strength of support (ref. 12) and determination of the activated surface of complex metal oxides (ref. 13) have also been reported. 

Determined that competitive adsorption between H2O and H2S inhibits H2S uptake by these mixed metal oxides. 

Although the sulfidation equilibria suggest that CuO/Cu20 should be able to reduce the H2S concentration in reformate below the 10 ppb DOE target, initial screening of various Cu-containing mixed metal oxides suggests that competitive adsorption between H2O and H2S may inhibit H2S uptake. As a consequence, the H2S concentration that... 

An Auger Electron Spectroscopy Study of SO2 Adsorption on Cerium-Zirconium Mixed Metal Oxides... 

Cerium-zirconium mixed metal oxides are used in conjunction with platinum group metals to reduce and eliminate pollutants in automotive emissions control catalyst systems. The ceria-zirconia promoter materials regulate the partial pressure of oxygen near the catalyst surface, thereby facilitating catalytic oxidation and reduction of gas phase pollutants. However, ceria-zirconia is particularly susceptible to chemical and physical deactivation through sulfur dioxide adsorption. The interaction of sulfur dioxide with ceria-zirconia model catalysts has been studied with Auger spectroscopy to develop fundamental information regarding the sulfur dioxide deactivation mechanism. 

Oxygen-containing compounds such as alcohols also undergo dissociative chemisorption, an example being the adsorption of gaseous methanol on molybdenum oxide catalysts (Eq. 5-28). Such metal oxides, and in particular mixed metal oxides, act as redox catalysts, as we shall see in Section 5.3.3. 

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