The aggregation of astaxanthin in hydrated methanol was kinetically studied in the temperature range from 10 ◦C to 50◦C, at different astaxanthin concentrations and solvent composition. A kinetic model for the formation and transformation of astaxanthin aggregated has been proposed. Spectrophotometric studies showed that monomeric astaxanthin decayed to H-aggregates that after-wards formed J-aggregates when water content was 50% and the temperature lower than 20 ◦C; at higher temperatures, very stable J-aggregates were formed directly. Monomer formed very stable H-aggregates when the water content was greater than 60%; in these conditions H-aggregates decayed into J-aggregates only when the temperature was at least 50 ◦C. Through these findings it was possible to establish that the aggregation reactions took place through a two steps consecutive reaction with first order kinetic constants and that the values of these depended on the solvent composition and temperature.

Kinetic model for astaxanthin aggregation in water-methanol mixtures

GIOVANNETTI, Rita;ALIBABAEI, Leila;PUCCIARELLI, Filippo
2009-01-01

Abstract

The aggregation of astaxanthin in hydrated methanol was kinetically studied in the temperature range from 10 ◦C to 50◦C, at different astaxanthin concentrations and solvent composition. A kinetic model for the formation and transformation of astaxanthin aggregated has been proposed. Spectrophotometric studies showed that monomeric astaxanthin decayed to H-aggregates that after-wards formed J-aggregates when water content was 50% and the temperature lower than 20 ◦C; at higher temperatures, very stable J-aggregates were formed directly. Monomer formed very stable H-aggregates when the water content was greater than 60%; in these conditions H-aggregates decayed into J-aggregates only when the temperature was at least 50 ◦C. Through these findings it was possible to establish that the aggregation reactions took place through a two steps consecutive reaction with first order kinetic constants and that the values of these depended on the solvent composition and temperature.
2009
262
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11581/112294
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