Silica-supported bimetallic Pt-Au catalysts prepared via different synthetic routes have been investigated in terms of their structural properties, adsorption of CO, and catalytic activity for the selective catalytic reduction of NO by propylene, the oxidation of propylene in the absence of NO, and the 16 O/ 18 O homoexchange reaction. Catalysts prepared by incipient wetness impregnation from individual Pt and Au precursors exhibited characteristics very similar to those of monometallic Pt catalysts, indicating that in these cases the presence of Au did not affect the catalytic performance of Pt in any significant way. This behavior is consistent with a model in which the two metals remain segregated due to their miscibility gap, and only Pt participates in the adsorption of CO and the reactions under consideration. In contrast, catalysts prepared from aPt 2 Au 4 (C≡C t Bu) 8 organo-bimetallic cluster precursor exhibited different behavior both in terms of CO adsorption and their catalytic activity for the three reactions examined. The combination of the kinetic, spectroscopic, and structural characterization data suggests that in this case Pt and Au remain intimately mixed in the form of Pt-Au bimetallic particles and that the presence of Au in these particles modifies the behavior of Pt.

Large amounts of post‐consumer carpet are discarded every year. Most of this waste is currently landfilled, while a small percentage is incinerated. The face carpet fibers, consisting primarily of nylon 6 and nylon 6,6, represent the majority component in the carpet waste. Recent financial incentives and environmental constraints have motivated the industrial sector to develop recycling strategies for these fibers. Depolymerization into their constituent monomers is the most complex recycling route, but at the same time it produces the most valuable product. A second alternative involves the use of solvents for the extraction of carpet fiber components in their polymeric form. Finally, a third recycling option yields thermoplastic mixtures by melt blending the carpet waste. The recent literature on the recycling of nylon from carpet waste is reviewed in this paper. The paper also includes a section focusing on the current state of carpet recycling at the Industrial level.

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A series of bimetallic Al2O3-supported Rh-Ge catalysts was prepared by surface redox reactions under controlled hydrogen atmosphere. The surface properties of these catalysts were probed via in-situ FTIR spectroscopic studies of adsorbed CO and were compared to those of monometallic Rh catalysts that had undergone similar treatments. The results indicate that Ge addition results in the formation and stabilization of smaller rhodium ensembles at the expense of larger Rh0 surfaces. A charge-transfer mechanism from Ge to Rh is also inferred by the IR results for the high Ge loading samples. Air exposure of the catalysts leads to an irreversible segregation of the two metals and formation of large Rh crystallites.