Chemical Reactions of Organic Compounds with X‐Ray Activated Water

1938 ◽  
Vol 6 (5) ◽  
pp. 229-240 ◽  
Author(s):  
Hugo Fricke ◽  
Edwin J. Hart ◽  
Homer P. Smith
Keyword(s):  
Organic Compounds ◽  
Chemical Reactions ◽  
X Ray

Chemical Reactions of Organic Compounds with X-Ray Activated Water

1962 ◽  
Vol 17 (3) ◽  
pp. 262 ◽  
Author(s):  
Hugo Fricke ◽  
Edwin J. Hart ◽  
Homer P. Smith
Keyword(s):  
Organic Compounds ◽  
Chemical Reactions ◽  
X Ray

Phase-partitioning and chemical reactions of low molecular weight organic compounds in fog

Tellus B ◽  
1992 ◽  
Vol 44 (5) ◽  
pp. 533-544 ◽  
Author(s):  
M. C. Facchini ◽  
S. Fuzzi ◽  
J. A. Lind ◽  
H. Fierlinger-Oberlinninger ◽  
M. Kalina ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Organic Compounds ◽  
Chemical Reactions ◽  
Low Molecular Weight ◽  
Phase Partitioning

Use of TALP with laboratory powder diffraction data from 2D detectors

2013 ◽  
Vol 28 (S2) ◽  
pp. S481-S490
Author(s):  
Oriol Vallcorba ◽  
Anna Crespi ◽  
Jordi Rius ◽  
Carles Miravitlles
Keyword(s):  
Organic Compounds ◽  
Structural Study ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Powder Pattern ◽  
Experimental Setup ◽  
Intensity Data ◽  
Powder Diffraction Data ◽  
X Ray ◽  
Molecular Compounds

The viability of the direct-space strategy TALP (Vallcorba et al., 2012b) to solve crystal structures of molecular compounds from laboratory powder diffraction data is shown. The procedure exploits the accurate metric refined from a ‘Bragg-Brentano’ powder pattern to extract later the intensity data from a second ‘texture-free’ powder pattern with the DAJUST software (Vallcorba et al., 2012a). The experimental setup for collecting this second pattern consists of a circularly collimated X-ray beam and a 2D detector. The sample is placed between two thin Mylar® foils, which reduces or even eliminates preferred orientation. With the combination of the DAJUST and TALP software a preliminary but rigorous structural study of organic compounds can be carried out at the laboratory level. In addition, the time-consuming filling of capillaries with diameters thinner than 0.3mm is avoided.

X-ray Microspectroscopy and Chemical Reactions in Soil Microsites

2011 ◽  
Vol 40 (3) ◽  
pp. 667-678 ◽  
Author(s):  
Dean Hesterberg ◽  
Martine C. Duff ◽  
Joe B. Dixon ◽  
Michael J. Vepraskas
Keyword(s):  
Chemical Reactions ◽  
X Ray

Identification of crystalline organic compounds by means of X-ray analysis

2010 ◽  
Vol 65 (12) ◽  
pp. 891-896 ◽  
Author(s):  
J. J. de Lange ◽  
J. P. W. Houtman
Keyword(s):  
Organic Compounds ◽  
X Ray

scholarly journals Chemical Bonding and the Sulfur K X-Ray Spectrum

1965 ◽  
Vol 9 ◽  
pp. 354-364 ◽  
Author(s):  
D. W. Wilbur ◽  
J. W. Gofman
Keyword(s):  
Electronic Structure ◽  
Single Crystal ◽  
Organic Compounds ◽  
Sulfur Atom ◽  
Chemical Bonding ◽  
Proportional Counter ◽  
Pulse Height ◽  
X Ray ◽  
Pulse Height Analysis ◽  
Chemical States

AbstractAn investigation has been made of the relative Kβ intensities in different chemical states of the sulfur atom using the Kα lines, with appropriate corrections, to provide the intensity standards. Both inorganic and organic compounds were included in the study. The data for each compound appear to be reliable to about ± 0.5%, while the whole series of compounds shows a variation greater than 20% in the corrected Kβ/Kα ratios. Energies were also measured, particularly the Kα energies, and their shifts were studied relative to the Kβ, intensity shifts. The work was done with a plane, single-crystal, helium-path spectrometer with proportional counter and pulse-height analysis for detection. The results are indicative of the usefulness of the method both in clarifying an uncertain chemical state and in studying the electronic structure of the bonded atom.

scholarly journals Catalytic Abatement of Volatile Organic Compounds and Soot over Manganese Oxide Catalysts

Materials ◽  
2021 ◽  
Vol 14 (16) ◽  
pp. 4534
Author(s):  
Miguel Jose Marin Figueredo ◽  
Clarissa Cocuzza ◽  
Samir Bensaid ◽  
Debora Fino ◽  
Marco Piumetti ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Low Temperature ◽  
Manganese Oxide ◽  
Organic Compounds ◽  
Catalytic Performance ◽  
Oxide Catalysts ◽  
X Ray ◽  
Manganese Oxide Catalysts ◽  
Volatile Organic ◽  
Temperature Programmed

A set of manganese oxide catalysts was synthesized via two preparation techniques: solution combustion synthesis (Mn3O4/Mn2O3-SCS and Mn2O3-SCS) and sol-gel synthesis (Mn2O3-SG550 and Mn2O3-SG650). The physicochemical properties of the catalysts were studied by means of N2-physisorption at −196 °C, X-ray powder diffraction, H2 temperature-programmed reduction (H2-TPR), soot-TPR, X-ray photoelectron spectroscopy (XPS) and field-emission scanning electron microscopy (FESEM). The high catalytic performance of the catalysts was verified in the oxidation of Volatile Organic Compounds (VOC) probe molecules (ethene and propene) and carbon soot in a temperature-programmed oxidation setup. The best catalytic performances in soot abatement were observed for the Mn2O3-SG550 and the Mn3O4/Mn2O3-SCS catalysts. The catalytic activity in VOC total oxidation was effectively correlated to the enhanced low-temperature reducibility of the catalysts and the abundant surface Oα-species. Likewise, low-temperature oxidation of soot in tight contact occurred over the Mn2O3-SG550 catalyst and was attributed to high amounts of surface Oα-species and better surface reducibility. For the soot oxidation in loose contact, the improved catalytic performance of the Mn3O4/Mn2O3-SCS catalyst was attributed to the beneficial effects of both the morphological structure that—like a filter—enhanced the capture of soot particles and to a probable high amount of surface acid-sites, which is characteristic of Mn3O4 catalysts.

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