Catalysts, general hydrogenations with colloidal

Recently, Chaudhari compared the activity of dispersed nanosized metal particles prepared by chemical or radiolytic reduction and stabilized by various polymers (PVP, PVA or poly(methylvinyl ether)) with the one of conventional supported metal catalysts in the partial hydrogenation of 2-butyne-l,4-diol. Several transition metals (e.g., Pd, Pt, Rh, Ru, Ni) were prepared according to conventional methods and subsequently investigated [89]. In general, the catalysts prepared by chemical reduction methods were more active than those prepared by radiolysis, and in all cases aqueous colloids showed a higher catalytic activity (up to 40-fold) in comparison with corresponding conventional catalysts. The best results were obtained with cubic Pd nanosized particles obtained by chemical reduction (Table 9.13). 

Hydrogenation of unsaturated carboxylic acids, such as acrylic, methacryUc, maleic, fumaric, cinnamic etc. acids was studied in aqueous solutions with a RhCU/TPPTS catalyst in the presence of p-CD and permethylated P-cyclodextrin [7]. In general, cyclodextrins caused an acceleration of these reactions. It is hard to make firm conclusions with regard the nature of this effect, since the catalyst itself is rather undefined (probably a phosphine-stabilized colloidal rhodium suspension, see 3.1.2) moreover the interaction of the substrates with the cyclodextrins was not studied separately. 

The formation and stabilization of noble metal colloids in the aqueous phase are widely known. Platinum and palladium are most widely used in hydrogenation of C=C bonds but some results have been described with rhodium. Generally, surfactants are investigated as stabilizers for the preparation of rhodium nanoparticles for biphasic catalysis in water. In many cases, ionic surfactants, such as ammonium salts, which provide sufficiently hydrophilic character to maintain the catalytic species within the aqueous phase, are used. The obtained micelles constitute interesting nanoreactors for the synthesis of controlled size nanoparticles due to the confinement of the particles inside the micelle cores. Aqueous colloidal solutions are then obtained and can be easily used as catalysts. 

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