scholarly journals Possibility of using pressure timing course from outlet nozzle of low-pressure impulse gas-phase injector to evaluate its flow properties

Author(s):  
Dariusz Szpica ◽  
Andrzej Borawski ◽  
Grzegorz Mieczkowski ◽  
Mohamed M. Awad ◽  
Ahmed Elgarayhi ◽  
...  
AIChE Journal ◽  
2015 ◽  
Vol 61 (11) ◽  
pp. 4013-4019 ◽  
Author(s):  
Galina Pavlovskaya ◽  
Joseph Six ◽  
Thomas Meersman ◽  
Navin Gopinathan ◽  
Sean P. Rigby

2019 ◽  
Vol 91 (7) ◽  
pp. 4429-4435 ◽  
Author(s):  
Christopher L. Suiter ◽  
Mark O. McLinden ◽  
Thomas J. Bruno ◽  
Jason A. Widegren

1987 ◽  
Vol 42 (3) ◽  
pp. 301-307 ◽  
Author(s):  
Hans Bock ◽  
Ralph Dammel

The HCl elimination from β-chloroethyl azide (1-azido-2-chloroethane) over potassium tert. butanolate at 350 K in a low pressure flow system is optimized using PE spectroscopic real-time gas analysis. The highly explosive vinyl azide formed can be purified by cool-trapping the by-products. Its subsequent and virtually hazard-free pyrolysis yields 2H-azirine, which can be isolated at temperatures below 240 K.In contrast, the direct pyrolysis of β-chloroethyl azide requires temperatures above 710 K and results in a simultaneous split-off of both HCl and N2, yielding acetonitrile as the main thermolysis product. No intermediates such as β-chloroethanimine or ketenimine are observed, a result which is interpreted in terms of chemical activation


1988 ◽  
Vol 135 (9) ◽  
pp. 2378-2379 ◽  
Author(s):  
Z. M. Qian ◽  
H. Michiel ◽  
A. Van Ammel ◽  
J. Nijs ◽  
R. Mertens

1985 ◽  
Vol 63 (1) ◽  
pp. 62-67 ◽  
Author(s):  
Hélène Deslauriers ◽  
Guy J. Collin

The photofragmentation of 2,3-dimethylbutene and 3,3-dimethylbutene has been studied at 147 and 184.9 nm in the gas phase. The main primary decomposition process at both wavelengths involves the rupture of a β(C—C) bond. The quantum yield for this process is higher than 0.7 at 147 nm and is probably even higher at 184.9 nm. All dimethallyl radicals formed at 147 nm in this process decompose at low pressure, but some of them isomerize from the α,β- to the α,α- structure (and vice versa) — via a 1,4-H transfer — before decomposition. At 184.9 nm, the same primary process is used to get a rough value for the lifetime of the photoexcited molecule, compared with the one made with RRKM calculations by assuming that all the photon energy resides in the vibrational framework of the fundamental electronic state. These lifetimes are about one nanosecond or less.


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