Deactivation, heterogeneous catalysis poisoning

Measurement of heat of adsorption by means of microcalorimetry has been used extensively in heterogeneous catalysis to gain more insight into the strength of gas-surface interactions and the catalytic properties of solid surfaces [61-65]. Microcalorimetry coupled with volumetry is undoubtedly the most reliable method, for two main reasons (i) the expected physical quantities (the heat evolved and the amount of adsorbed substance) are directly measured (ii) no hypotheses on the actual equilibrium of the system are needed. Moreover, besides the provided heat effects, adsorption microcalorimetry can contribute in the study of all phenomena, which can be involved in one catalyzed process (activation/deactivation of the catalyst, coke production, pore blocking, sintering, and adsorption of poisons in the feed gases) [66]. 

As in the case of homogeneous catalysis, poisons can also lead to deactivation of heterogeneous catalysts. Soluble or volatile metal or nitrogen compounds can destroy acid sites, while carbon monoxide and sulphur compounds almost invariably poison nickel and noble metal hydrogenation catalysts by bonding strongly with surface metal atoms. These considerations often lead to the selection of less active, but more poison-resistant, catalysts for industrial use. 

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