Capture of Gas-Phase Arsenic Oxide by Lime:  Kinetic and Mechanistic Studies

2001 ◽  
Vol 35 (4) ◽  
pp. 794-799 ◽  
Author(s):  
Raja A. Jadhav ◽  
Liang-Shih Fan
Keyword(s):  
Gas Phase ◽  
Mechanistic Studies ◽  
Arsenic Oxide

Mechanistic studies on gas-phase negative ion unimolecular decompositions. Alkoxide anions

1988 ◽  
Vol 110 (9) ◽  
pp. 2714-2722 ◽  
Author(s):  
William. Tumas ◽  
Robert F. Foster ◽  
John I. Brauman
Keyword(s):  
Gas Phase ◽  
Negative Ion ◽  
Mechanistic Studies

scholarly journals A new charge-tagged proline-based organocatalyst for mechanistic studies using electrospray mass spectrometry

2014 ◽  
Vol 10 ◽  
pp. 2027-2037 ◽  
Author(s):  
J Alexander Willms ◽  
Rita Beel ◽  
Martin L Schmidt ◽  
Christian Mundt ◽  
Marianne Engeser
Keyword(s):  
Mass Spectrometry ◽  
Gas Phase ◽  
Electrospray Mass Spectrometry ◽  
Temporal Evolution ◽  
Mechanistic Studies ◽  
Catalytic Center ◽  
Enamine Catalysis ◽  
Esi Mass Spectrometry ◽  
Catalyzed Reactions ◽  
Gas Phase Fragmentation

A new 4-hydroxy-L-proline derivative with a charged 1-ethylpyridinium-4-phenoxy substituent has been synthesized with the aim of facilitating mechanistic studies of proline-catalyzed reactions by ESI mass spectrometry. The charged residue ensures a strongly enhanced ESI response compared to neutral unmodified proline. The connection by a rigid linker fixes the position of the charge tag far away from the catalytic center in order to avoid unwanted interactions. The use of a charged catalyst leads to significantly enhanced ESI signal abundances for every catalyst-derived species which are the ones of highest interest present in a reacting solution. The new charged proline catalyst has been tested in the direct asymmetric inverse aldol reaction between aldehydes and diethyl ketomalonate. Two intermediates in accordance with the List–Houk mechanism for enamine catalysis have been detected and characterized by gas-phase fragmentation. In addition, their temporal evolution has been followed using a microreactor continuous-flow technique.

Fluorine Atom Production Mechanisms From COF2 and NF3 in Uv Laser Etching of Poly-Silicon and Molybdenum

1986 ◽  
Vol 75 ◽  
Author(s):  
Gary L. Loper ◽  
Martin D. Tabat
Keyword(s):  
Production Process ◽  
Gas Phase ◽  
Fluorine Atom ◽  
Charge Carriers ◽  
Uv Laser ◽  
Mechanistic Studies ◽  
Laser Etching ◽  
Microelectronic Devices ◽  
Film Layer ◽  
Production Mechanisms

AbstractUltraviolet laser-induced, radical-etching processes developed by us can provide practical etch rates and selectivities for most of the important film layer combinations used in silicon microelectronic devices. These processes have been demonstrated in simple proximity and projection exposure experiments to produce etch features on surfaces with dimensions of a few tenths of a micrometer.Mechanistic studies suggest that, in our etching processes for polysilicon and molybdenum, fluorine atoms responsible for etching are primarily produced from the precursors COF2 and NF3 on the surface rather than in the gas phase. The predominant production process appears to be photodecomposition of surface adsorbed precursor. Contributions due to precursor pyrolysis or precursor reaction with photogenerated charge carriers are found to be unimportant.

Thermal degradation events as health hazards: Particle vs gas phase effects, mechanistic studies with particles

1992 ◽  
Vol 27 ◽  
pp. 251-256 ◽  
Author(s):  
G. Oberdörster ◽  
J. Ferin ◽  
J. Finkelstein ◽  
S. Soderholm
Keyword(s):  
Thermal Degradation ◽  
Gas Phase ◽  
Health Hazards ◽  
Mechanistic Studies

Mechanistic studies of the role of formaldehyde in the gas-phase methylation of phenol

2008 ◽  
Vol 256 (2) ◽  
pp. 215-225 ◽  
Author(s):  
N BALLARINI ◽  
F CAVANI ◽  
L MASELLI ◽  
S PASSERI ◽  
S ROVINETTI
Keyword(s):  
Gas Phase ◽  
Mechanistic Studies

scholarly journals Kinetic and Mechanistic Studies for the Gas-phase Reaction of Ozone with 2, 3-Dimethyl-2-Butene and 1, 3-Butadiene

2017 ◽  
Vol 14 (3) ◽  
pp. 547-556
Author(s):  
Baghdad Science Journal
Keyword(s):  
Double Bond ◽  
Gas Phase ◽  
Rate Coefficients ◽  
Phase Reaction ◽  
Atmospheric Conditions ◽  
Absolute Rate ◽  
Mechanistic Studies ◽  
Methyl Group ◽  
Gas Phase Reaction ◽  
Good Agreement

The reactions of ozone with 2,3-Dimethyl-2-Butene (CH3)2C=C(CH3)2 and 1,3-Butadiene CH2=CHCH=CH2 have been investigated under atmospheric conditions at 298±3K in air using both relative and absolute rate techniques, and the measured rate coefficients are found to be in good agreement in both techniques used. The obtained results show the addition of ozone to the double bond in these compounds and how it acts as function of the methyl group substituent situated on the double bond. The yields of all the main products have been determined using FTIR and GC-FID and the product studies of these reactions establish a very good idea for the decomposition pathways for the primary formed compounds (ozonides) and give a good information for the effect of the methyl group on the degradation pathways. The results have been discussed from the view point of their importance in the atmospheric oxidation of these pollutants.

Sign in / Sign up

Export Citation Format

Share Document