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Inorganic Chemistry | 2010

Hexagonal Molybdenum Trioxide : Known for 100 Years and Still a Fount of New Discoveries

Hans-Joachim Lunk; Hans Hartl; Monika Hartl; Martin Fait; Ilya G. Shenderovich; Michael Feist; Timothy A. Frisk; Luke L. Daemen; Daniel Mauder; Reinhard Eckelt; Andrey A. Gurinov

In 1906, the preparation of “molybdic acid hydrate” was published by Arthur Rosenheim. Over the past 40 years, a multitude of isostructural compounds, which exist within a wide phase range of the system MoO3−NH3−H2O, have been published. The reported molecular formulas of “hexagonal molybdenum oxide” varied from MoO3 to MoO3·0.33NH3 to MoO3·nH2O (0.09 ≤ n ≤ 0.69) to MoO3·mNH3·nH2O (0.09 ≤ m ≤ 0.20; 0.18 ≤ n ≤ 0.60). Samples, prepared by the acidification route were investigated using thermal analysis coupled online to a mass spectrometer for evolved gas analysis, X-ray powder diffraction, Fourier transform infrared, Raman, magic-angle-spinning 1H- and 15N NMR spectroscopy, and incoherent inelastic neutron scattering. A comprehensive characterization of these samples will lead to a better understanding of their structure and physical properties as well as uncover the underlying relationship between the various compositions. The synthesized polymeric parent samples can be represented by the structural formula (NH4)(x∞)(3)[Mo(y square 1−y)O(3y)(OH)(x)(H2O)(m−n)]·nH2O with 0.10 ≤ x ≤ 0.14, 0.84 ≤ y ≤ 0.88, and m + n ≥ 3 − x − 3y. The X-ray study of a selected monocrystal confirmed the presence of the well-known 3D framework of edge- and corner-sharing MoO6 octahedra. The colorless monocrystal crystallizes in the hexagonal system with space group P6(3)/m, Z = 6, and unit cell parameters of a = 10.527(1) Å, c = 3.7245(7) Å, V = 357.44(8) Å3, and ρ = 3.73 g·cm(−3). The structure of the prepared monocrystal can best be described by the structural formula (NH4)(0.13∞)(3)[Mo(0.86 square 0.14)O2.58(OH)0.13(H2O)(0.29−n)]·nH2O, which is consistent with the existence of one vacancy (square) for six molybdenum sites. The sample MoO3·0.326NH3·0.343H2O, prepared by the ammoniation of a partially dehydrated MoO3·0.170NH3·0.153H2O with dry gaseous ammonia, accommodates NH3 in the hexagonal tunnels, in addition to [NH4]+ cations and H2O. The “chimie douce” reaction of MoO3·0.155NH3·0.440H2O with a 1:1 mixture of NO/NO2 at 100 °C resulted in the synthesis of MoO3·0.539H2O. This material is of great interest as a host of various molecules and cations.


Thermochimica Acta | 2008

Thermal decomposition of ammonium paratungstate tetrahydrate under non-reducing conditions: Characterization by thermal analysis, X-ray diffraction and spectroscopic methods

Martin Fait; H.-J. Lunk; Michael Feist; M. Schneider; J.N. Dann; Timothy A. Frisk


Archive | 1996

Process of making a non-sag tungsten wire for electric lamps

Martin Fait; Joachim Fuchs; Alfred-Georg Gahn; Hans-Joachim Lunk; Michael Salmen; Burkhard Ziemer


Thermochimica Acta | 2016

Thermal decomposition of ammonium paratungstate tetrahydrate: New insights by a combined thermal and kinetic analysis

Martin Fait; Elena Moukhina; Michael Feist; Hans-Joachim Lunk


Archive | 1996

Method of manufacturing a non-sag tungsten wire for electric lamps

Michael Salmen; Hans-Joachim Lunk; Alfred-Georg Gahn; Bernhard Altmann; Martin Fait


Archive | 2006

Catalyst for the synthesis of dimethyl carbonate in the gas phase

Reinhard Eckelt; Martin Fait; Rolf Fricke; Manfred Richter


European Journal of Inorganic Chemistry | 2012

Thermal Decomposition of Ammonium Paratungstate Tetrahydrate Traced by In Situ UV/Vis Diffuse Reflectance Spectroscopy

Martin Fait; Hans-Joachim Lunk


Thermochimica Acta | 2016

Surface tungsten reduction during thermal decomposition of ammonium paratungstate tetrahydrate in oxidising atmosphere: A paradox?

Martin Fait; Jörg Radnik; Hans-Joachim Lunk


Archive | 1996

Potassium-doped tungsten wire esp. for incandescent lamp filament

Michael Salmen; Hans-Joachim Lunk; Alfred Gahn; Bernhard Altmann; Martin Fait


Archive | 2006

Katalysator zur Synthese von Dimethylcarbonat in der Gasphase

Reinhard Eckelt; Martin Fait; Rolf Fricke; Manfred Richter

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Michael Feist

Humboldt University of Berlin

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Joachim Fuchs

Humboldt State University

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Daniel Mauder

Free University of Berlin

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