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FIBER OPTICAL MICRO-DETECTORS FOR OXYGEN SENSING IN POWER PLANTS
Author(s) -
Gregory L. Baker,
Ruby N. Ghosh,
D. J. Osborn,
Po Zhang
Publication year - 2005
Publication title -
osti oai (u.s. department of energy office of scientific and technical information)
Language(s) - English
Resource type - Reports
DOI - 10.2172/842719
Subject(s) - materials science , oxygen sensor , optical fiber , oxygen permeability , oxygen , quenching (fluorescence) , composite number , sol gel , luminescence , molybdenum , fiber , analytical chemistry (journal) , chemical engineering , composite material , optoelectronics , optics , nanotechnology , chemistry , metallurgy , chromatography , fluorescence , physics , organic chemistry , engineering
A reflection mode fiber optic oxygen sensor is being developed that can operate at high temperatures for power plant applications. The sensor is based on the {sup 3}O{sub 2} quenching of the red emission from hexanuclear molybdenum chloride clusters. Two critical materials issues are the cluster's ability to withstand high temperatures when immobilized in a porous the sol-gel support, and whether after heating to high temperatures, the sol-gel matrix maintains a high and constant permeability to oxygen to support rapid quenching of luminescence. We used a composite materials approach to prepare stable sensing layers on optical fibers. We dispersed 60 w/w% of a pre-cured sol-gel composite containing the potassium salt of molybdenum clusters (K{sub 2}Mo{sub 6}Cl{sub 14}) into a sol-gel binder solution, and established the conditions necessary for deposition of sol-gel films on optical fibers and planar substrates. The fiber sensor has an output signal of 5 nW when pumped with an inexpensive commercial 365 nm ultraviolet light emitting diode (LED). Quenching of the sensor signal by oxygen was observed up to a gas temperature of 175 C with no degradation of the oxygen permeability of the composite after high temperature cycling. On planar substrates the cluster containing composite responds within <1 second to a gas exchange from nitrogen to oxygen, indicating the feasibility of real-time oxygen detection

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