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Adsorption of Natural Organic Polyelectrolytes by Activated Carbon: A Size-Exclusion Chromatography Study

Kilduff, James E., Karanfil, Tanju, Chin, Yu-Ping, Weber, Walter J.·1996·Environmental Science & Technology

Abstract

The adsorption of several different organic polyelectrolytes from aqueous solution by activated carbon was characterized. Polyelectrolytes included humic acids extracted from peat and soil, polymaleic acid, a synthetic polymer identified as a fulvic acid surrogate, and natural organic matter in Huron River (Ann Arbor, MI) water. Isotherms of individual ultrafiltration size fractions confirmed that smaller molecular size components adsorb to a greater extent on an adsorbent mass basis. The molecular weight distributions of organic polyelectrolytes remaining in solution after equilibration with various amounts of activated carbon were measured with high-performance size-exclusion chromatography (HPSEC). A comparison of molecular weight distributions demonstrated conclusively that small molecular size components are adsorbed preferentially; i.e., adsorptive fractionation on the basis of molecular size occurs. This behavior was observed for each of the wide variety of samples studied, suggesting that it may be a rather general feature of the adsorption of polyelectrolyte mixtures from solution by activated carbon.

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Metadata

Authors
Kilduff, J. E., Karanfil, T., Chin, Y.-P., & Weber, W. J.
Venue
Environmental Science & Technology
Published
1996-03-01
Volume
30
Issue
4
Pages
1336-1343
ISSN
  • 0013-936X (ISSN-L)
  • 1520-5851
OpenAlex
W2053275409
Cited by
196
References
0
FWCI
12.52
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Adsorption of Natural Organic Polyelectrolytes by Activated Carbon: A Size-Exclusion Chromatography Study. https://app.cochat.ai/papers/10.1021/es950547r
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Kilduff, J. E., Karanfil, T., Chin, Y.-P., & Weber, W. J. (1996). Adsorption of Natural Organic Polyelectrolytes by Activated Carbon: A Size-Exclusion Chromatography Study. Environmental Science & Technology. https://doi.org/10.1021/es950547r

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