z-logo
Premium
Analytical method for determing copper in edible shortenings and oils
Author(s) -
Deck Rudolph E.,
Kaiser Kay K.
Publication year - 1970
Publication title -
journal of the american oil chemists' society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.512
H-Index - 117
eISSN - 1558-9331
pISSN - 0003-021X
DOI - 10.1007/bf02640401
Subject(s) - copper , reagent , chemistry , boiling , chromatography , relative standard deviation , organic chemistry , detection limit
A reliable, practical method was developed for the quantitative determination of sub‐ppm levels of copper in edible shortenings and oils. Copper is quantitatively extracted with a boiling solution of 0.01% EDTA in 25% HCl. The extract was analyzed with 2,9‐dimethyl‐4,7‐diphenyl‐1,10‐phenanthroline (Bathocuproine), a highly specific and exceptionally sensitive reagent for the colorimetric determination of copper. An average recovery of 99.8% was obtained on 22 samples containing added oil soluble copper standards. A standard deviation of 0.002 ppm was established at the 0.05 ppm level during routine application of this method to a variety of shortenings and oils.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom