Activated Carbons from Eucalyptus Wood. Influence of the Carbonization Temperature
- 1 April 1997
- journal article
- research article
- Published by Taylor & Francis in Separation Science and Technology
- Vol. 32 (6) , 1115-1126
- https://doi.org/10.1080/01496399708000950
Abstract
CO2 activation of eucalyptus wood chars obtained at 400, 600, and 800°C has been studied. The carbonization stage develops an incipient microporosity. The micropore volume and width increase with increasing temperature. Partial gasification of these chars with CO2 allows one to obtain activated carbons which show differences in micropore size distribution depending on the temperature at which the starting char was obtained. No significant effect on mesoporosity development was noticed whereas lower macropore volumes were obtained with activated carbons resulting from the char prepared at the highest temperature (800°C).Keywords
This publication has 13 references indexed in Scilit:
- Activated carbons from carbon dioxide partial gasification of eucalyptus kraft ligninEnergy & Fuels, 1993
- Preparation and characterization of activated carbons from eucalyptus kraft ligninCarbon, 1993
- CO2-reactivity of eucalyptus kraft lignin charsCarbon, 1993
- Adsorption of nitrogen by porous and non-porous carbonsCarbon, 1987
- Combined effects of inorganic constituents and pyrolysis conditions on the gasification reactivity of coal charsFuel Processing Technology, 1985
- Reporting physisorption data for gas/solid systems with special reference to the determination of surface area and porosity (Recommendations 1984)Pure and Applied Chemistry, 1985
- Method for the calculation of effective pore size distribution in molecular sieve carbon.JOURNAL OF CHEMICAL ENGINEERING OF JAPAN, 1983
- Studies on pore systems in catalysts V. The t methodJournal of Catalysis, 1965
- Computation of Pore Sizes from Physical Adsorption DataThe Journal of Physical Chemistry, 1953
- The Determination of Pore Volume and Area Distributions in Porous Substances. I. Computations from Nitrogen IsothermsJournal of the American Chemical Society, 1951