Sorption hysteresis of benzene in charcoal particles

被引:294
作者
Braida, WJ
Pignatello, JJ
Lu, YF
Ravikovitch, PI
Neimark, AV
Xing, BS
机构
[1] Connecticut Agr Expt Stn, Dept Soil & Water, New Haven, CT 06504 USA
[2] TRI Princeton, Princeton, NJ 08542 USA
[3] Univ Massachusetts, Dept Plant & Soil Sci, Amherst, MA 01003 USA
关键词
D O I
10.1021/es020660z
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
decreasesCharcoal is found in water, soil and sediment where it may act as a sorbent of organic pollutants. The sorption of organic compounds to natural solids often shows hysteresis. The purpose of this study was to determine the source of pronounced hysteresis that we found in the sorption of a hydrophobic compound (benzene) in water to a maplewood charcoal prepared by oxygen-limited pyrolysis at 673 K. Gas adsorption (N-2, Ar, CO2), C-13 NMR, and FTIR show the charcoal to be a microporous solid composed primarily of elemental (aromatic) C and secondarily of carboxyl and phenolic C. Nonlocal density functional theory (N2, Ar) and Monte Carlo (CO2) calculations reveal a porosity of 0.15 cm(3)/g, specific surface area of 400m(2)/g,and appreciable porosity in ultramicropores <10Angstrom. Benzene sorption-desorption conditions were chosen to eliminate artificial causes of hysteresis (rate-limiting diffusion, degradation, colloids effect). Charcoal sorbed up to its own weight of benzene at similar to69% of benzene water solubility. Sorption was highly irreversible over most of the range tested (10(-4)-10(3) mug/mL). A dimensionless irreversibility index (l) (0 : 1 :5 1) based on local slopes of adsorption and desorption branches was evaluated at numerous places along the isotherm. /(1) decreases as C increases, from 0.9-1 at low concentration to similar to0 (similar tofully reversible) at the highest concentrations. Using sedimentation and volumetric displacement measurements, benzene is observed to cause pronounced swelling (up to >2-fold) of the charcoal particles. It is proposed that hysteresis is due to pore deformation by the solute, which results in the pathway of sorption being different than the pathway of desorption and which leads to entrapment of some adsorbate as the polyaromatic scaffold collapses during desorption. It is suggested that intra-charcoal mass transport may be influenced by structural rearrangement of the solid, in addition to molecular diffusion.
引用
收藏
页码:409 / 417
页数:9
相关论文
共 54 条
[1]  
Barrer R.M., 1978, ZEOLITES CLAY MINERA
[2]   SOME ASPECTS OF THE SURFACE-CHEMISTRY OF CARBON-BLACKS AND OTHER CARBONS [J].
BOEHM, HP .
CARBON, 1994, 32 (05) :759-769
[3]   THE IMPORTANCE OF SPHEROIDAL CARBONACEOUS PARTICLES (SCPS) FOR THE DISTRIBUTION OF PARTICULATE POLYCYCLIC AROMATIC-HYDROCARBONS (PAHS) IN AN ESTUARINE-LIKE URBAN COASTAL WATER AREA [J].
BROMAN, D ;
NAF, C ;
WIK, M ;
RENBERG, I .
CHEMOSPHERE, 1990, 21 (1-2) :69-77
[4]   Adsorption of gases in multimolecular layers [J].
Brunauer, S ;
Emmett, PH ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 :309-319
[5]   Quantification of the soot-water distribution coefficient of PAHs provides mechanistic basis for enhanced sorption observations [J].
Bucheli, TD ;
Gustafsson, Ö .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (24) :5144-5151
[6]   Model of micropore closure in hard carbon prepared from sucrose [J].
Buiel, ER ;
George, AE ;
Dahn, JR .
CARBON, 1999, 37 (09) :1399-1407
[7]   Sorption-desorption of imidacloprid and its metabolites in soils [J].
Cox, L ;
Koskinen, WC ;
Yen, PY .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1997, 45 (04) :1468-1472
[8]  
EVERETT DH, 1967, SOLID GAS INTERFACE, V2, pCH36
[9]   Black carbon in soils: the use of benzenecarboxylic acids as specific markers [J].
Glaser, B ;
Haumaier, L ;
Guggenberger, G ;
Zech, W .
ORGANIC GEOCHEMISTRY, 1998, 29 (04) :811-819
[10]  
Goldberg E. D., 1985, Black carbon in the environment. Properties and distribution