Picture of athlete cycling

Open Access research with a real impact on health...

The Strathprints institutional repository is a digital archive of University of Strathclyde's Open Access research outputs. Strathprints provides access to thousands of Open Access research papers by Strathclyde researchers, including by researchers from the Physical Activity for Health Group based within the School of Psychological Sciences & Health. Research here seeks to better understand how and why physical activity improves health, gain a better understanding of the amount, intensity, and type of physical activity needed for health benefits, and evaluate the effect of interventions to promote physical activity.

Explore open research content by Physical Activity for Health...

Secondary coking and cracking of shale oil vapors from pyrolysis or hydropyrolysis of a Kentucky Cleveland oil-shale in a 2-stage reactor

Carter, S.D. and Citiroglu, M. and Gallacher, J.G. and Snape, Colin and Mitchell, S. and Lafferty, C.J. (1994) Secondary coking and cracking of shale oil vapors from pyrolysis or hydropyrolysis of a Kentucky Cleveland oil-shale in a 2-stage reactor. Fuel, 73 (9). pp. 1455-1458. ISSN 0016-2361

Full text not available in this repository. Request a copy from the Strathclyde author

Abstract

It is widely recognized that secondary reactions which are mainly associated with minerals during oil shale retorting have a marked influence on the product yields and compositions. To understand these phenomena more clearly, the secondary reactions of shale oil vapours from the pyrolysis (or hydropyrolysis) of Kentucky Cleveland oil shale were examined in a two-stage, fixed-bed reactor in flowing nitrogen or hydrogen at pressures of 0.1-15 MPa. The vapours from pyrolysis (first stage) were passed through a second stage containing combusted shale, upgrading catalyst or neither. Carbon conversion to volatile products in the first stage increased from 49% during thermal pyrolysis to 81% at 15 MPa H2 partial pressure. During thermal pyrolysis, total pressure had only a slight effect on carbon removal from the raw shale and subsequent deposition on to the porous solids in the second stage. Carbon deposition on to the combusted shale in the second stage was reduced to zero at 15 MPa H2 partial pressure. The n-alkane distributions of the oils as determined by gas chromatography clearly demonstrated that higher hydrogen pressure, contact with combusted shale, or both contributed to lower-molecular-weight products.