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Physical and chemical studies of chlorophyll in microemulsions. Progress report

Technical Report ·
DOI:https://doi.org/10.2172/6890397· OSTI ID:6890397
Studies designed to provide fundamental information on both the nature of photoreactions in microemulsions and the utility of these media as solvents for absorbers of solar energy were conducted. As a test system, the photoreduction of absorbed dye (principally methyl red) sensitized by chlorophyll a in an anionic mineral oil in water microemulsion was investiged. Using ascorbate as the water soluble reducing agent and pigment concentrations of up to eight per drop (10mM), the reaction exhibits a pseudo zero order dependence on methyl red. The effect of sensitizer, ascorbate concentration and light intensity on the quantum yield was examined, as well as the effect of varying the microemulsion charge type, product catalysis, and the use of synthetic porphyrin sensitizers. In microemulsions containing up to eight chlorophyll molecules per microdroplet, the quantum yield remains constant over five orders of magnitude concentration. The intrinsic quantum yield is independent of droplet surface charge, but is dependent on pH. One of the products of the chemical reduction of methyl red, N, N-dimethyl-p-phenylenediamine (DMPD), increases the limiting quantum yield two to three fold. Synthetic porphyrins have been found to act as sensitizers, and a number of tetrapyridyl porphyrin derivatives containing one to four carbon chains of varying length have been made and examined. The results show that the quantum yield increases with increasing chain length for the monoalkyl compounds, and also indicate the possible involvement of a sensitizer orientation effect. The transport of oil soluble electroactive species in nonionic microemulsions has been found to exhibit percolation behavior, which has potential photogalvanic applications.
Research Organization:
Drexel Univ., Philadelphia, PA (USA). Dept. of Chemistry
Sponsoring Organization:
USDOE
DOE Contract Number:
AS02-77ER04452
OSTI ID:
6890397
Report Number(s):
DOE/ER/04452-3
Country of Publication:
United States
Language:
English