TY - JOUR
T1 - Importance of catalyst dispersion in the gasification of lignite chars
AU - Radovic, Ljubisa R.
AU - Walker, Philip L.
AU - Jenkins, Robert G.
N1 - Funding Information:
This study was supportedb y the Gas ResearchI nsti-tute, under Contract 5014-363-023I5n.i tial supportf or LRR in the form of a Fulbright Scholarship was provided by the Yugoslav-American Commissionf or Ed-ucationalE xchange. The assistanceo f Dr. Katarzyna Steczko in the preparation of samples is gratefully acknowledgedT. hanks are also due to Dr. L. Schmitt, of American Cyanamid, for the XPS work. The ele- mental analyses were performed by the staff of the Mineral ConstitutionL aboratory of The Pennsylvania State University. The coal samples were obtained from the Coal Research Section of The Pennsylvania State University.
PY - 1983/8
Y1 - 1983/8
N2 - Lignite chars were prepared in N2 under widely varying conditions of pyrolysis heating rate, temperature, and residence time. Their reactivities were measured by isothermal thermogravimetric analysis in 0.1 MPa air. A major decrease in char reactivity was observed with increasing severity of heat-treatment conditions. The relatively high gasification reactivity of lignite chars, compared to those obtained from higher rank coals, is due to the catalytic effect of the initially very highly dispersed CaO on the char surface. Char deactivation is caused primarily by CaO crystallite growth, measured by X-ray diffraction line broadening. When the reactivities of the various chars are expressed as turnover frequencies, i.e., per unit catalyst site, differences in observed rates of about 200 times are reduced to within 1 order of magnitude. Thus, it has been shown that the commonly observed and heretofore empirically treated lignite char deactivation with increasing severity of pyrolysis conditions can be correlated with a decrease in a measurable fundamental property of the chars: catalyst dispersion.
AB - Lignite chars were prepared in N2 under widely varying conditions of pyrolysis heating rate, temperature, and residence time. Their reactivities were measured by isothermal thermogravimetric analysis in 0.1 MPa air. A major decrease in char reactivity was observed with increasing severity of heat-treatment conditions. The relatively high gasification reactivity of lignite chars, compared to those obtained from higher rank coals, is due to the catalytic effect of the initially very highly dispersed CaO on the char surface. Char deactivation is caused primarily by CaO crystallite growth, measured by X-ray diffraction line broadening. When the reactivities of the various chars are expressed as turnover frequencies, i.e., per unit catalyst site, differences in observed rates of about 200 times are reduced to within 1 order of magnitude. Thus, it has been shown that the commonly observed and heretofore empirically treated lignite char deactivation with increasing severity of pyrolysis conditions can be correlated with a decrease in a measurable fundamental property of the chars: catalyst dispersion.
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U2 - 10.1016/0021-9517(83)90205-1
DO - 10.1016/0021-9517(83)90205-1
M3 - Article
AN - SCOPUS:0001261166
SN - 0021-9517
VL - 82
SP - 382
EP - 394
JO - Journal of Catalysis
JF - Journal of Catalysis
IS - 2
ER -