Gas-Phase Mixing and Dispersion in a Diffusion Furnace

2004 ◽  
Vol 151 (1) ◽  
pp. G24 ◽  
Author(s):  
Joseph J. Biernacki ◽  
Ramkumar Subramanian ◽  
Mohammed R. Islam ◽  
Casey Schewe ◽  
Michael C. Rogers
Keyword(s):  
Gas Phase ◽  
Phase Mixing

Gas phase mixing due to resonant acoustic oscillations in a cavity

1995 ◽  
Author(s):  
L Matta ◽  
C Zhu ◽  
J Jagoda ◽  
B Zinn
Keyword(s):  
Gas Phase ◽  
Acoustic Oscillations ◽  
Phase Mixing

scholarly journals Supplementary material to "High gas-phase mixing ratios of formic and acetic acid in the High Arctic"

2018 ◽  
Author(s):  
Emma L. Mungall ◽  
Jonathan P. D. Abbatt ◽  
Jeremy J. B. Wentzell ◽  
Gregory R. Wentworth ◽  
Jennifer G. Murphy ◽  
...  
Keyword(s):  
Acetic Acid ◽  
Gas Phase ◽  
High Arctic ◽  
Phase Mixing ◽  
Mixing Ratios ◽  
Supplementary Material

Estimation of gas phase mixing in packed beds

2008 ◽  
Vol 153 (1-2) ◽  
pp. 137-148 ◽  
Author(s):  
S. Frigerio ◽  
H. Thunman ◽  
B. Leckner ◽  
S. Hermansson
Keyword(s):  
Gas Phase ◽  
Packed Beds ◽  
Phase Mixing

scholarly journals Gas-phase mixing in bubble columns.

1989 ◽  
Vol 22 (2) ◽  
pp. 136-142 ◽  
Author(s):  
Mikio Kawagoe ◽  
Tsutao Otake ◽  
Campbell W. Robinson
Keyword(s):  
Gas Phase ◽  
Bubble Columns ◽  
Phase Mixing

Gas-Phase Mixing in Droplet Arrays

2010 ◽  
pp. 409-415
Author(s):  
M. R. G. Zoby ◽  
S. Navarro-Martinez ◽  
A. Kronenburg ◽  
A. J. Marquis
Keyword(s):  
Gas Phase ◽  
Phase Mixing

Experimental Study of Process Emissions From Atomic Layer Deposition of Al2O3 Under Various Temperatures and Purge Time

2017 ◽  
Vol 139 (5) ◽  
Author(s):  
Lulu Ma ◽  
Dongqing Pan ◽  
Yuanyuan Xie ◽  
Fenfen Wang ◽  
Chris Yuan
Keyword(s):  
Atomic Layer Deposition ◽  
Gas Phase ◽  
Environmental Sustainability ◽  
Atomic Layer ◽  
Experimental Investigations ◽  
Phase Mixing ◽  
Sustainability Performance ◽  
Layer Deposition ◽  
Time Changes ◽  
Time Of Reaction

Experimental investigations of process emissions from atomic layer deposition (ALD) of Al2O3 are accomplished under various temperatures and purge times to understand its environmental sustainability performance. About 93% of Trimethylaluminum (TMA) is found flowing through ALD system without deposition. 2–9 × 104 of ultrafine nanoparticles containing 51.9 ± 4.6% of C, 16.6 ± 0.9% of Al, 31.4 ± 4.1% of O are generated during each cycle of reactions. 0.34–0.38 cm3 of CH4 (25 °C, 1 atm), which takes up 45–51% of C contained in TMA is produced simultaneously. The concentration of nanoparticles drops with the increase of purge time. CH4 also has a trend of decreasing but acts more complex with the largest emission at a short purge time. Compared with temperature, which has limited effects on reactants, purge time changes the time of reaction as well as the degree of gas phase mixing, and therefore greatly influences ALD emissions.

Deuterium Incorporation into Glow-Discharge Deposited Deuterated-Hydrogenated Amorphous Silicon

1995 ◽  
Vol 377 ◽  
Author(s):  
L. S. Sidhu ◽  
F. Gaspari ◽  
S. K. O'Leary ◽  
S. Zukotynski
Keyword(s):  
Glow Discharge ◽  
Amorphous Silicon ◽  
Gas Phase ◽  
Hydrogenated Amorphous Silicon ◽  
Growth Surface ◽  
Direct Reaction ◽  
Deuterium Incorporation ◽  
Phase Mixing ◽  
Dominant Process ◽  
Hydrogenated Amorphous

ABSTRACTWe investigate deuterium incorporation into deuterated-hydrogenated amorphous silicon grown by the saddle-field glow-discharge of deuterium and silane. The presence of HD and SiH3D in the discharge suggests strong gas phase mixing. The dominant process of deuterium incorporation into the growing film appears to be the direct reaction between deuterium and the growth surface.

The photoelectron spectra of the methylbromamines and unsubstituted bromamines

1979 ◽  
Vol 57 (11) ◽  
pp. 1279-1285 ◽  
Author(s):  
D. Colbourne ◽  
D. C. Frost ◽  
C. A. McDowell ◽  
N. P. C. Westwood
Keyword(s):  
Gas Phase ◽  
Photoelectron Spectra ◽  
Phase Mixing

HeI photoelectron spectra are reported for pure gas-phase samples of the unstable methylbromamines, CH3NHBr, CH3NBr2, and (CH3)2NBr. Results are also presented for the unsubstituted bromamines NH2Br and NHBr2 obtained as products from a gas-phase mixing of NH3 and Br2. The spectra are compared with those of the corresponding chloramines.

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