TY - JOUR
T1 - TiO2/ZnO mixed oxide catalysts, characterization by x-ray photoelectron and infrared-spectroscopy and reactions with propanol and butanol
AU - A. Lercher, Johannes
AU - Vinek, Hannelore
AU - Noller, Heinrich
AU - Stoch, Jerzy
PY - 1984
Y1 - 1984
N2 - TiO2/ZnO mixed oxide catalysts, prepared by hydrolysis of chlorides, were characterized by X-ray photoelectron and infrared spectroscopy as well as by catalytic elimination reactions of propanol and butanol. XPS measurements suggest one phase present in all oxides (ZnTiO3), another only in oxides with 64 and 95 mole % ZnO. This unidentified phase is rather rich in ZnO, has oxygen of very high binding energy (Ols = 533 eV) and decomposes (or is modified) at temperatures above 500° C. I.r. adsorbate spectra of pyridine indicate that Ti4+ cations are mainly present on the surface of the ZnTiO3 phase, Zn2+ on the surface of the other. The changes in product distribution of elimination reactions are discussed in terms of varying acid - base properties.
AB - TiO2/ZnO mixed oxide catalysts, prepared by hydrolysis of chlorides, were characterized by X-ray photoelectron and infrared spectroscopy as well as by catalytic elimination reactions of propanol and butanol. XPS measurements suggest one phase present in all oxides (ZnTiO3), another only in oxides with 64 and 95 mole % ZnO. This unidentified phase is rather rich in ZnO, has oxygen of very high binding energy (Ols = 533 eV) and decomposes (or is modified) at temperatures above 500° C. I.r. adsorbate spectra of pyridine indicate that Ti4+ cations are mainly present on the surface of the ZnTiO3 phase, Zn2+ on the surface of the other. The changes in product distribution of elimination reactions are discussed in terms of varying acid - base properties.
UR - http://www.scopus.com/inward/record.url?scp=0021522497&partnerID=8YFLogxK
U2 - 10.1016/S0166-9834(00)81669-3
DO - 10.1016/S0166-9834(00)81669-3
M3 - Article
AN - SCOPUS:0021522497
SN - 0166-9834
VL - 12
SP - 293
EP - 307
JO - Applied Catalysis
JF - Applied Catalysis
IS - 4
ER -