Size fractionation of humic substances: Effect on protonation and metal binding properties
โ Scribed by H.Kipton J. Powell; Eric Fenton
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 990 KB
- Volume
- 334
- Category
- Article
- ISSN
- 0003-2670
No coin nor oath required. For personal study only.
โฆ Synopsis
Humic substances
have been extracted from a standard reference peat at pH 2.0, 6.0-6.5, 9.0 and 12.0 using 0.01 M or 0.001 M Na4P207. Humic acids extracted at pH 6.0, 9.0 and 12.0 showed a progressive increase in mean molecular size, as determined by gel permeation chromatography. With increasing molecular size there was a significant decrease in titratable acidity for humic acids (ca. 5.243 meq -COOHg-'). However, little variation in Cu(I1) binding strength or complexation capacity (gHS)-' was observed between humic acids (or between fulvic acids) extracted at different pH values. Likewise, there was little variation in the protonation constants when calculated on the basis of a discrete binding site model. The major differences were between fulvic and humic fractions. Fulvic acids had (i) a lower Cu(I1) binding strength, (ii) a lower complexation capacity per mol titratable COOH acidity (when batch extracted at pH >6), (iii) a higher titratable acidity (ca. 7.2 (vs. 4.7)meq -COOH g-l), (iv) a lower proportion of polyprotic (n>4) binding sites and (v) a larger fraction of strongly dissociating -COOH groups (42-58% with pK, ca. 2).
๐ SIMILAR VOLUMES
## Abstract The presence of dissolved humic substances (HS, fulvic and humic acids) generally reduces the up take of hydrophobic organic compounds into aquatic organisms. The extent of this effect depends both on the concentration and on the origin of the HS. The aim of this study was to investigat
The electroendosmotic flow (EOF), generated by the migration of solvated ions near the charged capillary surface, is an important factor in determining the capillary electrophoretic behaviour of humic substances (HS). We investigated the electrophoretic mobilities of HS fractions of reduced molecula