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Journal of the Chemical Society, Faraday Transactions | 1995

Acidity of aluminophosphate structures. Part 1.—Incorporation of sillicon into chabazite-like structure 44

Ursula Lohse; Barbara Parlitz; Bernd Altrichter; Karin Jancke; Elke Löuffler; Ellen Schreier; Fritz Vogt

SAPO-44 samples have been prepared with different silicon contents up to 34.3 mass% SiO2. Characterization of the samples by X-ray diffraction (XRD), thermal analysis, adsorption measurements, chemical analysis, microprobe analysis and IR spectroscopy reveals that the samples are highly crystalline, even those with the highest SiO2 content. The number of Bronsted acid sites determined by NH3 sorption [calorimetric and temperature-programmed desorption (TPD) measurements] is independent of the SiO2 content of the samples and amounts to about one acid centre per double-six-ring of the chabazite-like structure.Concerning the silicon ordering within the framework, it is proposed that aluminophosphate-based as well as aluminosilicate-based double-six-rings form the structure.


Journal of the Chemical Society, Faraday Transactions | 1993

Catalytical conversion of silicon tetrachloride to trichlorosilane. Characterization of the nickel silicalite catalyst by ferromagnetic resonance spectroscopy

Wolfgang Mörke; Fritz Vogt; Klaus-Peter Wendlandt; Holger Walter; Gerhard Roewer

The formation of nickel silicide in the reaction between nickel supported on silicalite and a gas mixture (molar ratio, H2 : SiCl4= 6 : 1) is studied. By ferromagnetic resonance (FMR) based Curie temperature measurements, it was determined that the formation of metal silicides starts at 723 K. From the signal intensity, it follows that the Si content of the silicides increases with increasing temperature from ca. 1 atom% at 723 K up to 6 atom% at 865 K. The geff values suggest the presence of two kinds of alloy containing ca. 1 atom% Si: one kind, produced at temperatures up to 723 K, forms a shell layer at the surface of the Ni metal particle, and the other, generated by decomposition of silicon-rich silicides formed at 865 K, is homogeneously alloyed over the whole particle.


Zeitschrift für anorganische und allgemeine Chemie | 1983

Untersuchungen an oxidischen Katalysatoren. XXXIV. Redoxverhalten des Nickels in NiNaY‐Zeolithen 1. Reduzierbarkeit und Reoxydierbarkeit von Nickel in NiNaY‐Zeolithen

Hartmut Lausch; W. Mörke; Fritz Vogt; H. Bremer


Archive | 1990

Two=stage prodn. of tri:chloro-silane from silicon tetra:chloride - by catalytic hydrogenation to silicon@ and hydrogen chloride, then reaction with silicon@

Rolf Dipl Chem Dr Re Teichmann; Hans Dipl Chem Dr Rer Kraemer; Johannes Dipl Chem Dr R Brumme; Detlef Jaeckel; Gerhard Roewer; Wolfgang Dipl Chem Dr Horlbeck; Fritz Vogt; Klaus-Peter Dipl Ch Wendtlandt


Zeitschrift für Chemie | 2010

Untersuchungen zum Reduktionsverhalten modifizierter NaNiY‐Zeolithkatalysatoren

H. Bremer; Karl-Heinz Bager; Fritz Vogt


Zeitschrift für anorganische und allgemeine Chemie | 1983

Untersuchungen an oxidischen Katalysatoren. XXXV. Redoxverhalten des Nickels in NiNaY-Zeolithen 2. Untersuchungen zur Dispersität von Ni- und Ni/NiO-Teilchen in reduzierten und reoxydierten NiNaY-Proben

H. Lausch; Fritz Vogt; H. Bremer


Zeitschrift für Chemie | 2010

Magnetische Eigenschaften von NaCuY-, NaCoY- und NaNiY-Zeolithen

H. Bremer; Rainer Schöudel; Fritz Vogt; A. M. Rubinštejn; A. A. Slinkin; G. A. Fedorovskaja


Zeitschrift für Chemie | 2010

FT‐IR‐spektroskopische Untersuchung der Wechselwirkung von CO mit Cu2+‐Ionen in Zeolithen

Fritz Vogt; Issam Achkar; Klaus-Peter Wendlandt; Hartmut Hobert; Michael Meier


Zeitschrift für Chemie | 2010

Charakterisierung des Nickels in polykationischen NiNaY-Zeolithen mittels der Röntgen-Photoelektronenspektroskopie (XPS)

Ch. M. Minačev; G. V. Antošin; E. S. Špiro; Fritz Vogt; Karl-Heinz Bager; H. Bremer


Zeitschrift für anorganische und allgemeine Chemie | 1984

Untersuchungen an oxidischen Katalysatoren. XLI. Redoxverhalten des Nickels in NiNa–Y-Zeolithen 3. Reduzierbarkeit von Ni2+ -Ionen und Eigenschaften des reduzierten Nickels in aciden NiNa–Y-Zeolithen†

Fritz Vogt; U.‐D. Pitzing; L. Peitzsch; H. Bremer

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H. Bremer

Technische Hochschule

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