Formation of catalytically active copper and nickel nanoparticles in natural zeolites; 4th FEZA Conference, Collège de France, Paris, France, september, 2-6, 2008

Bibliographische Detailangaben
Parent link:4th FEZA Conference, Collège de France, Paris, France, september, 2-6, 2008.— 2008.— PI-C05
Weitere Verfasser: Petranovskii V., Pestryakov A. N. Aleksey Nikolaevich, Kazantseva L. K., Cruz J., Kryazhov A. N.
Zusammenfassung:Structure, thermostability and catalytic properties of copper and nickel nanoparticles in natural and synthetic zeolites have been studied using methods of XRD, elemental analysis, UV-visible spectroscopy, MAS NMR, TEM and catalytic testing. Different states of Cu have been identified by UV-Vis spectroscopy: Cu+ and Cu2+ ions, O-Cu-O and Cu-O-Cu complexes and Cu nanoparticles. Measurements of synthetic zeolites showed that shape and position of plasma resonance band depend on the acidity of zeolite supports. The most acid mordenites with Si/Al≈7-10 prevents formation of copper nanoparticles while Cu2+ is reduced to Cu+ and few atomic Cun clusters. Less acid erionite, clinoptilolite and mordenites with high Si/Al ratio promote formation of Cu nanoparticles. For Ni-exchanged zeolites spectra typical for Ni(H2O)62+ are observed. The spectra changed with increasing temperature due to dehydration of Ni2+ coordination sphere and replacement of H2O ligand molecules by oxygen atoms of zeolite framework. The catalytic experiments demonstrate that the temperature of beginning of hydrocarbons conversion starts in 170-250°C range, depending on the composition of the catalyst. The complete conversion can be observed for all zeolites, depending (probably) on Si/Al ratio of the zeolite matrix. No destruction of crystalline structure was observed from XRD and 27Al MAS NMR spectra under conditions used for catalytic tests.
В фонде НТБ ТПУ отсутствует
Sprache:Englisch
Veröffentlicht: 2008
Schlagworte:
Format: Buchkapitel
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=599112

MARC

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200 1 |a Formation of catalytically active copper and nickel nanoparticles in natural zeolites  |f V. Petranovskii [et al.] 
330 |a Structure, thermostability and catalytic properties of copper and nickel nanoparticles in natural and synthetic zeolites have been studied using methods of XRD, elemental analysis, UV-visible spectroscopy, MAS NMR, TEM and catalytic testing. Different states of Cu have been identified by UV-Vis spectroscopy: Cu+ and Cu2+ ions, O-Cu-O and Cu-O-Cu complexes and Cu nanoparticles. Measurements of synthetic zeolites showed that shape and position of plasma resonance band depend on the acidity of zeolite supports. The most acid mordenites with Si/Al≈7-10 prevents formation of copper nanoparticles while Cu2+ is reduced to Cu+ and few atomic Cun clusters. Less acid erionite, clinoptilolite and mordenites with high Si/Al ratio promote formation of Cu nanoparticles. For Ni-exchanged zeolites spectra typical for Ni(H2O)62+ are observed. The spectra changed with increasing temperature due to dehydration of Ni2+ coordination sphere and replacement of H2O ligand molecules by oxygen atoms of zeolite framework. The catalytic experiments demonstrate that the temperature of beginning of hydrocarbons conversion starts in 170-250°C range, depending on the composition of the catalyst. The complete conversion can be observed for all zeolites, depending (probably) on Si/Al ratio of the zeolite matrix. No destruction of crystalline structure was observed from XRD and 27Al MAS NMR spectra under conditions used for catalytic tests. 
333 |a В фонде НТБ ТПУ отсутствует 
463 |t 4th FEZA Conference, Collège de France, Paris, France, september, 2-6, 2008  |o book of abstracts and recent research reports  |v PI-C05  |d 2008 
610 1 |a труды учёных ТПУ 
701 1 |a Petranovskii  |b V. 
701 1 |a Pestryakov  |b A. N.  |c Chemist  |c Professor of Tomsk Polytechnic University, Doctor of Chemical Science  |f 1963-  |g Aleksey Nikolaevich  |3 (RuTPU)RU\TPU\pers\30471  |4 070  |9 14796 
701 1 |a Kazantseva  |b L. K. 
701 1 |a Cruz  |b J. 
701 1 |a Kryazhov  |b A. N. 
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801 2 |a RU  |b 63413507  |c 20130328  |g RCR 
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