Journal of Water Resource and Protection

Volume 2, Issue 3 (March 2010)

ISSN Print: 1945-3094   ISSN Online: 1945-3108

Google-based Impact Factor: 1.65  Citations  

Removal of Hydrophobic Organic Contaminants from Aqueous Solutions by Sorption onto Biodegradable Polyesters

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DOI: 10.4236/jwarp.2010.23024    4,892 Downloads   9,884 Views  Citations

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ABSTRACT

Sorption by biodegradable polyesters of several aromatic chemicals as model compounds for hydrophobic organic contaminants (HOCs) was studied. The biodegradable polyesters used were poly(butylene succinate), poly(3-hydroxybutyrate-co-3-hydroxyvalerate), poly(ε-caprolactone), poly(butylene succinate/ terephthalate), and poly(L-lactic acid). Petrochemical plastics, low-density polyethylene and polyethylene terephtalate, were used for comparison. The target HOCs were biphenyl, bisphenol-A, dibenzofuran, diethylstilbestrol, nonyl-phenol, and chlorophenols. The treatment of the HOC solutions with each of the biodegradable polyesters resulted in the nearly complete removal of the chemicals by sorption from the aqueous phase, except for the case of poly(L-lactic acid). Low-density polyethylene adsorbed biphenyl and dibenzofuran selectively, and polyethylene terephtalate did not adsorb any of the HOCs. The adsorptive interaction between the plastics and the HOCs might be related to both the glass transition temperature of the former and the nature of the latter as defined by the Fujita's inorganicity/organicity ratio. The toxic effect of 3,5-dichlorophenol on bacte-rial growth in liquid culture was removed by the addition of a biodegradable polyester. These results provide a basis for the applicability of the biodegradable plastics as the adsorbents for the removal of HOCs from aquatic environments.

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Matsuzawa, Y. , Kimura, Z. , Nishimura, Y. , Shibayama, M. and Hiraishi, A. (2010) Removal of Hydrophobic Organic Contaminants from Aqueous Solutions by Sorption onto Biodegradable Polyesters. Journal of Water Resource and Protection, 2, 214-221. doi: 10.4236/jwarp.2010.23024.

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