The utilization of in situ DRIFT spectroscopy combined with advanced thermoanalytical techniques (temperature programmed decomposition, TPDE; temperature programmed oxidative decomposition, TPOD) allows the characterization of redox behavior of copper ions inside ZSM-5 zeolites. The oxidation of carbonaceous impurities inside the solid matrix to CO and CO2 is demonstrated to be responsible for Cu(ii)--> Cu(i) reduction, since the formation of other oxidation products, namely O-2, H2O2 or O-2(-) ions, was not detected by mass spectrometry and DRIFT. The unusual kinetics of CO evolution in thermoanalytical experiments was attributed to the formation of a relatively stable Cu+... CO adduct characterized by a typical IR band at 2157 cm(-1), which acts as a specific active site of a chromatographic adsorbent material.
In situ analytical investigation of redox behavior of Cu-ZSM-5 catalysts / Carlo, Dossi; Sandro, Recchia; Andrea, Pozzi; Achille, Fusi; Vladimiro, Dalsanto; Moretti, Giuliano. - In: PHYSICAL CHEMISTRY CHEMICAL PHYSICS. - ISSN 1463-9076. - 1:18(1999), pp. 4515-4519. [10.1039/a905222d]
In situ analytical investigation of redox behavior of Cu-ZSM-5 catalysts
MORETTI, GIULIANO
1999
Abstract
The utilization of in situ DRIFT spectroscopy combined with advanced thermoanalytical techniques (temperature programmed decomposition, TPDE; temperature programmed oxidative decomposition, TPOD) allows the characterization of redox behavior of copper ions inside ZSM-5 zeolites. The oxidation of carbonaceous impurities inside the solid matrix to CO and CO2 is demonstrated to be responsible for Cu(ii)--> Cu(i) reduction, since the formation of other oxidation products, namely O-2, H2O2 or O-2(-) ions, was not detected by mass spectrometry and DRIFT. The unusual kinetics of CO evolution in thermoanalytical experiments was attributed to the formation of a relatively stable Cu+... CO adduct characterized by a typical IR band at 2157 cm(-1), which acts as a specific active site of a chromatographic adsorbent material.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


