TY - JOUR
T1 - Tailoring activated carbons for enhanced removal of natural organic matter from natural waters
AU - Dastgheib, Seyed A.
AU - Karanfil, Tanju
AU - Cheng, Wei
N1 - Funding Information:
This work was supported in part by a research grant (R-828-045-01-0) from the United States Environmental Protection Agency’s Science to Achieve Results (STAR) program (Office of Research and Development, National Center for Environmental Research and Quality) and in part by a research grant from National Science Foundation (BES 0093600). However, the manuscript has not been subjected to the peer and policy review of these agencies and therefore does not necessarily reflect their views.
PY - 2004
Y1 - 2004
N2 - Several pathways have been employed to systematically modify two granular activated carbons (GACs), F400 (coal-based) and Macro (wood-based), for examining adsorption of dissolved natural organic matter (DOM) from natural waters. A total of 24 activated carbons with different physical and chemical characteristics was produced. The impact of carbon treatment on the DOM adsorption was examined by conducting isotherm experiments at a neutral pH using the modified carbons and a DOM isolated from the influent to Myrtle Beach drinking water treatment plant in South Carolina (USA). Adsorption of the DOM by two activated carbon fibers, with relatively uniform pore size distributions, showed that only pores with widths larger than 1 nm were accessible to the DOM macromolecules. Increases in the carbon supermicropore and mesopore volume (i.e., > 1 nm) increased the DOM uptake, if the surface chemistry was favorable. The isotherms normalized on a surface area basis showed the significance of carbon surface chemistry on the DOM uptake. At neutral pH, adsorption of negatively charged DOM molecules was favored by basic and positively charged surfaces, while the DOM uptake was minimized when the surface had acidic characteristics. High temperature ammonia treatment of oxidized carbons considerably enhanced the DOM uptake, mainly due to the increase in accessible surface area and surface basicity. Iron-impregnated carbons indicated an enhanced affinity of iron-laden carbon surface toward the DOM species, if the surface was not negatively charged.
AB - Several pathways have been employed to systematically modify two granular activated carbons (GACs), F400 (coal-based) and Macro (wood-based), for examining adsorption of dissolved natural organic matter (DOM) from natural waters. A total of 24 activated carbons with different physical and chemical characteristics was produced. The impact of carbon treatment on the DOM adsorption was examined by conducting isotherm experiments at a neutral pH using the modified carbons and a DOM isolated from the influent to Myrtle Beach drinking water treatment plant in South Carolina (USA). Adsorption of the DOM by two activated carbon fibers, with relatively uniform pore size distributions, showed that only pores with widths larger than 1 nm were accessible to the DOM macromolecules. Increases in the carbon supermicropore and mesopore volume (i.e., > 1 nm) increased the DOM uptake, if the surface chemistry was favorable. The isotherms normalized on a surface area basis showed the significance of carbon surface chemistry on the DOM uptake. At neutral pH, adsorption of negatively charged DOM molecules was favored by basic and positively charged surfaces, while the DOM uptake was minimized when the surface had acidic characteristics. High temperature ammonia treatment of oxidized carbons considerably enhanced the DOM uptake, mainly due to the increase in accessible surface area and surface basicity. Iron-impregnated carbons indicated an enhanced affinity of iron-laden carbon surface toward the DOM species, if the surface was not negatively charged.
KW - A. Activated carbon
KW - B. Surface treatment
KW - D. Adsorption properties
KW - Impregnation
KW - Surface chemistry
UR - http://www.scopus.com/inward/record.url?scp=1042288953&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=1042288953&partnerID=8YFLogxK
U2 - 10.1016/j.carbon.2003.12.062
DO - 10.1016/j.carbon.2003.12.062
M3 - Article
AN - SCOPUS:1042288953
SN - 0008-6223
VL - 42
SP - 547
EP - 557
JO - Carbon
JF - Carbon
IS - 3
ER -