New Ca-sequestering materials based on the oxidation of the hydrolysis products of lactose

Citation
A. Abbadi et al., New Ca-sequestering materials based on the oxidation of the hydrolysis products of lactose, GREEN CHEM, 1(5), 1999, pp. 231-235
Citations number
27
Categorie Soggetti
Chemistry
Journal title
GREEN CHEMISTRY
ISSN journal
14639262 → ACNP
Volume
1
Issue
5
Year of publication
1999
Pages
231 - 235
Database
ISI
SICI code
1463-9262(199910)1:5<231:NCMBOT>2.0.ZU;2-E
Abstract
The Ca-sequestering capacity of the equimolar mixture of aldonic acids or a ldaric acids obtained by selective catalytic oxidation of the hydrolysis pr oducts of lactose (D-glucose and D-galactose) was determined using a Ca ion selective electrode. Also, the Ca-sequestering capacity of each component of these mixtures was quantified. The addition of boric acid at pH = 10 enh anced the Ca-sequestering capacity substantially, especially for D-gluconic acid and D-glucaric acid. Apparently the configuration of the vicinal diol moiety at the 3,4-position is of major importance in defining the Ca-seque stering capacity of aldonic and aldaric acids in the presence of borate. Th e effect of the concentration of NaOH on the Ca-sequestering capacity was e valuated in the range of 1-5 wt.% by titration with 0.1 M calcium acetate. The polyhydroxycarboxylic acids exhibit an optimum Ca-sequestering capacity up to one mol Ca ions per mol carboxylate group at these high pHs.