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Redox behavior of transition metal ions in zeolites 6. Reversibility of the reduction reaction in silver zeolites

Abstract

Degassing above 573/sup 0/K of Ag-Y or Ag-mordenite previously reduced by hydrogen at 623/sup 0/K resulted in hydrogen evolution, the amount of hydrogen increasing to a maximum at about 873/sup 0/K. No hydrogen was evolved when the zeolite was reduced by hydrazine or hydroxylamine, indicating that hydrogen is formed by reaction between silver metal and hydroxyl groups formed in the reduction step (i.e., the reverse of the reduction step). Consumption of hydroxyl groups was proven by IR studies of pyridine chemisorption which occurs entirely as pyridinium ions on Broensted sites or reduced samples but with increasing formation of pyridine on Lewis acid sites as the degassing temperature increases; formation of silver(I) ions was proven by carbon monoxide complexation. Silver metal outside the zeolite pores was not affected by the degassing, and the amount of hydrogen evolved upon degassing decreased with increasing number of reduction-degassing cycles, probably as a result of dehydroxylation or sintering. Spectra, graphs, tables, and 21 references.
Publication Date:
Jan 01, 1977
Product Type:
Journal Article
Reference Number:
EDB-83-161117
Resource Relation:
Journal Name: J. Chem. Soc., Faraday Trans. 1; (United Kingdom); Journal Volume: 73:11
Subject:
37 INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; SILVER; REDOX REACTIONS; TRANSITION ELEMENTS; ZEOLITES; REDUCTION; ABSORPTION SPECTROSCOPY; CARBON MONOXIDE; CATALYSIS; CATALYSTS; CHEMISORPTION; HIGH TEMPERATURE; HYDROGEN; LEWIS ACIDS; OXIDATION; OXYGEN COMPOUNDS; CARBON COMPOUNDS; CARBON OXIDES; CHALCOGENIDES; CHEMICAL REACTIONS; ELEMENTS; HYDROGEN COMPOUNDS; INORGANIC ACIDS; INORGANIC ION EXCHANGERS; ION EXCHANGE MATERIALS; MATERIALS; METALS; MINERALS; NONMETALS; OXIDES; SEPARATION PROCESSES; SORPTION; SPECTROSCOPY; 400201* - Chemical & Physicochemical Properties; 400301 - Organic Chemistry- Chemical & Physicochemical Properties- (-1987)
OSTI ID:
5770157
Research Organizations:
Univ. of Kath., Leuven, Belgium
Country of Origin:
United Kingdom
Language:
English
Other Identifying Numbers:
Journal ID: CODEN: JCFTA
Submitting Site:
HEDB
Size:
Pages: 1755-1762
Announcement Date:
Apr 01, 1983

Citation Formats

Jacobs, P A, Uytterhoeven, J B, and Beyer, H K. Redox behavior of transition metal ions in zeolites 6. Reversibility of the reduction reaction in silver zeolites. United Kingdom: N. p., 1977. Web. doi:10.1039/f19777301755.
Jacobs, P A, Uytterhoeven, J B, & Beyer, H K. Redox behavior of transition metal ions in zeolites 6. Reversibility of the reduction reaction in silver zeolites. United Kingdom. https://doi.org/10.1039/f19777301755
Jacobs, P A, Uytterhoeven, J B, and Beyer, H K. 1977. "Redox behavior of transition metal ions in zeolites 6. Reversibility of the reduction reaction in silver zeolites." United Kingdom. https://doi.org/10.1039/f19777301755.
@misc{etde_5770157,
title = {Redox behavior of transition metal ions in zeolites 6. Reversibility of the reduction reaction in silver zeolites}
author = {Jacobs, P A, Uytterhoeven, J B, and Beyer, H K}
abstractNote = {Degassing above 573/sup 0/K of Ag-Y or Ag-mordenite previously reduced by hydrogen at 623/sup 0/K resulted in hydrogen evolution, the amount of hydrogen increasing to a maximum at about 873/sup 0/K. No hydrogen was evolved when the zeolite was reduced by hydrazine or hydroxylamine, indicating that hydrogen is formed by reaction between silver metal and hydroxyl groups formed in the reduction step (i.e., the reverse of the reduction step). Consumption of hydroxyl groups was proven by IR studies of pyridine chemisorption which occurs entirely as pyridinium ions on Broensted sites or reduced samples but with increasing formation of pyridine on Lewis acid sites as the degassing temperature increases; formation of silver(I) ions was proven by carbon monoxide complexation. Silver metal outside the zeolite pores was not affected by the degassing, and the amount of hydrogen evolved upon degassing decreased with increasing number of reduction-degassing cycles, probably as a result of dehydroxylation or sintering. Spectra, graphs, tables, and 21 references.}
doi = {10.1039/f19777301755}
journal = []
volume = {73:11}
journal type = {AC}
place = {United Kingdom}
year = {1977}
month = {Jan}
}