Abstract
Carrageenan in milk and milk products was precipitated by adding Rivanol to the system at pH 4-6. Under these conditions, the milk proteins were precipitated simul- taneously. The combined carrageenan- Rivanol and milk proteins-Rivanol precip- itates were separated by eentrifugation and washed with 0.2% Rivanol in 0.05 ~ acetic acid, to remove inorganic sulfate. The washed precipitate was hydrolyzed with tiC1, decolorized with carbon and interfer- ing cations in the hydrolyate removed with Dowex 50W-X8 resin (H ÷ form, 50-100 mesh). The sulfate content of the deionized hydrotyate, after adjustment to pH 4.0, was determined in a buffered system (pH 4.0) with barium ehloranilate. The red color developed was measured at 530 m~. The influence of several variables affecting both the precipitation of the carrageenan and the eolorimetric determination was examined.