Gas phase pyrolysis of coal-related aromatic compounds in a coiled tube flow reactor

Fuel ◽  
1988 ◽  
Vol 67 (3) ◽  
pp. 334-340 ◽  
Author(s):  
Odolphus S.L. Bruinsma ◽  
Peter J.J. Tromp ◽  
Henry J.J. de Sauvage Nolting ◽  
Jacob A. Moulijn
Fuel ◽  
1988 ◽  
Vol 67 (3) ◽  
pp. 327-333 ◽  
Author(s):  
Odolphus S.L. Bruinsma ◽  
Rob S. Geertsma ◽  
Pim Bank ◽  
Jacob A. Moulijn

2019 ◽  
Vol 18 (2) ◽  
pp. 314-318 ◽  
Author(s):  
Martin Dilla ◽  
Ahmet E. Becerikli ◽  
Alina Jakubowski ◽  
Robert Schlögl ◽  
Simon Ristig

Newly developed tubular reactor geometry allows intensive gas–solid interaction in photocatalytic gas-phase CO2 reduction.


1996 ◽  
Vol 03 (01) ◽  
pp. 807-811 ◽  
Author(s):  
M. EHBRECHT ◽  
H. FERKEL ◽  
V.V. SMIRNOV ◽  
O. STELMAKH ◽  
W. ZHANG ◽  
...  

A newly developed technique is employed for the production of carbon and silicon cluster beams starting from gaseous compounds. It is based on the CO 2-laser-induced decomposition of molecular gases containing carbon and silicon, such as CO 2H2 and SiH 4, in a flow reactor. In order to decompose acetylene, SF 6 is used as a sensitizer. By introducing a skimmer into the reaction zone, the generated silicon and carbon clusters are transferred to free molecular flow and analyzed with a time-of-flight mass spectrometer. It is shown that the technique can be efficiently employed to produce fullerenes C 60 and C 70 and, in the case of silicon, ultrapure nanosized particles of up to 3-nm diameter.


2016 ◽  
Vol 41 (4) ◽  
pp. 418-427 ◽  
Author(s):  
David Lokhat ◽  
Maciej Starzak ◽  
Deresh Ramjugernath

The gas-phase reaction of hexafluoropropene and molecular oxygen was investigated in a tubular flow reactor at 450 kPa and within a temperature range of 463–493 K using HFP/O2 mixtures containing 20–67% HFP on a molar basis. Capillary and packed column chromatography served as the main analytical technique. The reaction yielded HFPO, COF2, CF3COF, C2F4 and c-C3F6 as gas-phase products. High molecular weight oligomers were also formed. The oligomers were found to have a polyoxadifluoromethylene structure according to elemental and 19F NMR analysis. At 493 K HFP is proposed to undergo oxygen-mediated decomposition to difluorocarbene radicals, yielding greater quantities of difluorocarbene recombination products. Kinetic parameters for a revised model of the oxidation process were identified through least squares analysis of the experimental data.


2017 ◽  
Vol 4 (6) ◽  
pp. 1115-1121 ◽  
Author(s):  
Felix Rechberger ◽  
Markus Niederberger

A newly developed prototype of a flow reactor enables the exploitation of nanoparticle based aerogel monoliths as macroscopically sized photocatalysts in gas phase reactions.


2016 ◽  
Vol 18 (22) ◽  
pp. 15118-15132 ◽  
Author(s):  
Chantal Sleiman ◽  
Sergio González ◽  
Stephen J. Klippenstein ◽  
Dahbia Talbi ◽  
Gisèle El Dib ◽  
...  

The gas phase reaction between the CN radical and acetonitrile CH3CN was investigated experimentally with a CRESU apparatus and a slow flow reactor as well as theoretically to explore the temperature and pressure dependence of its rate coefficient from 354 K down to 23 K.


2014 ◽  
Vol 14 (13) ◽  
pp. 19395-19429
Author(s):  
L. Zhang ◽  
I. Cheng ◽  
D. Muir ◽  
J.-P. Charland

Abstract. Athabasca oil sands industry in northern Alberta, Canada is a possible source of polycyclic aromatic compounds (PACs). Monitored PACs, including polycyclic aromatic hydrocarbons (PAHs), alkylated PAHs, and dibenzothiophenes, in precipitation and in air at three near-source sites in the Fort MacKay and Fort McMurray area during May 2011 to August 2012 were analyzed to generate a database of scavenging (or washout) ratios (Wt) for PACs scavenged by both snow and rain. Median precipitation and air concentrations of parent PAHs over the May 2011 to August 2012 period ranged from 0.3–184.9 (chrysene) ng L−1 and 0.01–3.9 (naphthalene) ng m−3, respectively, which were comparable to literature values. Higher concentrations in precipitation and air were observed for alkylated PAHs and dibenzothiophenes. The median precipitation and air concentrations were 11.3–646.7 (C3-fluoranthene/pyrene) ng L−1 and 0.21–16.9 (C3-naphthalene) ng m−3, respectively, for alkylated PAHs, and 8.5–530.5 (C4-dibenzothiophene) ng L−1 and 0.13–6.6 (C2-dibenzothiophene) ng m−3 for dibenzothiophenes and their alkylated derivatives. Median Wt over the measurement period were 6100–1.1 × 106 from snow scavenging and 350–2.3 × 105 from rain scavenging depending on the PAC species. Median Wt for parent PAHs were within the range of those observed at other urban and suburban locations. But Wt for acenaphthylene in snow samples was 2–7 times higher. Some individual snow and rain samples exceeded literature values by a factor of 10. Wt for benzo(a)pyrene, dibenz(a,h)anthracene, and benzo(g,h,i)perylene in snow samples had reached 107, which is the maximum for PAH snow scavenging ratios reported in literature. From the analysis of data subsets, Wt for particulate-phase dominant PACs were 14–20 times greater than gas-phase dominant PACs in snow samples and 7–20 times greater than gas-phase dominant PACs in rain samples. Wt from snow scavenging was ∼9 times greater than rain scavenging for particulate-phase dominant PACs and 4–9.6 times greater than rain scavenging for gas-phase dominant PACs. Gas-particle fractions of each PAC, particle size distributions of particulate-phase dominant PACs, and Henry's Law constant of gas-phase dominant PACs explained, to a large extent, the different Wt values among the different PACs and precipitation types. This study verified findings from a previous study of Wang et al. (2014) which suggested that snow scavenging is more efficient than rain scavenging of particles for equivalent precipitation amount, and also provided new knowledge on the scavenging of gas-phase PACs by snow and rain.


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