Publication Details

Category Text Publication
Reference Category Journals
DOI 10.1002/etc.5620210902
Document Shareable Link
Title (Primary) Validation of a modified Flory-Huggins concept for description of hydrophobic organic compound sorption on dissolved humic substances
Author Georgi, A.; Kopinke, F.-D.
Source Titel Environmental Toxicology and Chemistry
Year 2002
Department TUCHEM
Volume 21
Issue 9
Page From 1766
Page To 1774
Language englisch
Abstract Sorption coefficients (K-DOC) on dissolved organic matter (DOM) have been determined by means of solid-phase microextraction (SPME) for hydrophobic organic compounds (HOCs) of various classes, for example, polycyclic aromatic hydrocarbons (PAHs), noncondensed arenes, and alkanes. Relating the K-DOC values obtained to the octanol-water partition coefficients of the solutes results in class-specific correlations. Obviously, PAHs have a higher affinity to DOM than other HOCs with equal K-OW values. The different K-DOC to K-OW correlations can be combined into one general formula based on a modified Flory-Huggins concept. It permits the calculation of sorption coefficients from the solubility parameters (8) and K-OW values of the solutes and the solubility parameter of the sorbent. The latter value, which is specific to the DOM under consideration, can be determined from a single measured sorption coefficient. By applying the proposed Flory-Huggins concept, which is based on the presumption of nonspecific interactions between HOCs and DOM, the different affinities of PAHs, noncondensed arenes, and alkanes to DOM can be accurately predicted.
Persistent UFZ Identifier https://www.ufz.de/index.php?en=20939&ufzPublicationIdentifier=5506
Georgi, A., Kopinke, F.-D. (2002):
Validation of a modified Flory-Huggins concept for description of hydrophobic organic compound sorption on dissolved humic substances
Environ. Toxicol. Chem. 21 (9), 1766 - 1774 10.1002/etc.5620210902