Catalysts, bifunctional reforming oxide

Cobalt is used to promote CO oxidation in reformers [284, 285], suggesting PtCo alloys may be useful catalysts for H2 oxidation in the presence of CO. PtCo alloys have been proposed as improved methanol oxidation catalysts [286] because cobalt may assist with CO removal (CO is an intermediate in meflianol electrooxidation) through a mechanism analogous to the PtRu bifunctional mechanism. PtCo alloys have also been studied as improved ORR catalysts [200, 287, 288]. In addition to their improved ORR kinetics, these alloys have been shown to be more tolerant to methanol crossover in direct methanol fuel cells (DMFCs), again possibly through improved CO removal kinetics [289]. However, Stevens et al. [235] observed no impact on CO-stripping with the addition of eobalt to Pt, and explained this as due to surface cobalt dissolving away. 

Catalytic processes frequently require more than a single chemical function, and these bifunctional or polyfunctional materials innst be prepared in away to assure effective communication among the various constitnents. For example, naphtha reforming requires both an acidic function for isomerization and alkylation and a hydrogenation function for aromati-zation and saturation. The acidic function is often a promoted porous metal oxide (e.g., alumina) with a noble metal (e.g., platinum) deposited on its surface to provide the hydrogenation sites. To avoid separation problems, it is not unusual to attach homogeneous catalysts and even enzymes to solid surfaces for use in flow reactors. Although this technique works well in some environmental catalytic systems, such attachment sometimes modifies the catalytic specifici-... 

We have explored rare earth oxide-modified amorphous silica-aluminas as "permanent" intermediate strength acids used as supports for bifunctional catalysts. The addition of well dispersed weakly basic rare earth oxides "titrates" the stronger acid sites of amorphous silica-alumina and lowers the acid strength to the level shown by halided aluminas. Physical and chemical probes, as well as model olefin and paraffin isomerization reactions show that acid strength can be adjusted close to that of chlorided and fluorided aluminas. Metal activity is inhibited relative to halided alumina catalysts, which limits the direct metal-catalyzed dehydrocyclization reactions during paraffin reforming but does not interfere with hydroisomerization reactions. 

Some of the typical reforming reactions catalyzed by the bifunctional, metal-acidic oxide catalysts, along with a specific example of each, are listed below ... 

A well-known cooperation effect is due to bifunctional catalysis in catalytic reforming, both Pt and alumina carry out part of the catalytic work. Several other types of cooperation have been mentioned in the last years, e.g. between catalysts within zeolitic structures and another component (1-3) or between separate oxide phases in oxidation or related reactions (4-12). Explanations for these cooperations often rest on spill over processes (13-15). 

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