2005
DOI: 10.1088/1742-6596/15/1/042
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Hazardous gas detection with an integrating sphere in the near-infrared

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Cited by 10 publications
(8 citation statements)
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“…Luminescent sensors often have long delay times and so are not suited to exhaust gas sensing where the concentrations change rapidly. A wide range of absorption-based techniques exist including a whole range of evanescent wave gas sensors [8]- [11], single-pass cell sensors [12], [13] and multipass cell sensors [14]- [16]. Evanescent wave gas sensors can have sensitivity issues as the interaction between the optical light and the test gas is often very limited.…”
Section: Introductionmentioning
confidence: 99%
“…Luminescent sensors often have long delay times and so are not suited to exhaust gas sensing where the concentrations change rapidly. A wide range of absorption-based techniques exist including a whole range of evanescent wave gas sensors [8]- [11], single-pass cell sensors [12], [13] and multipass cell sensors [14]- [16]. Evanescent wave gas sensors can have sensitivity issues as the interaction between the optical light and the test gas is often very limited.…”
Section: Introductionmentioning
confidence: 99%
“…With the improvement of light power, the PA signal also increases, but high-power light sources usually have high cost and large volumes. Some researchers have used devices in which light beams are reflected multiple times to achieve the equivalent effects [ 30 , 31 , 32 , 33 , 34 ]. Lassen reported a photoacoustic sensor based on an integrating sphere.…”
Section: Introductionmentioning
confidence: 99%
“…In 1996, Tranchart et al 9 used an integrating sphere in combination with tunable diode laser spectroscopy at l = 830 nm and 1200 nm to detect water vapour and butane, respectively. A significant number of works launched by Hawe of the University of Limerick has resulted in a broadband spectroscopic sensor for CO 2 in 2005 (at 1590 nm) 10 and in 2007 (at 1570 nm and 2000 nm) 11 with a detection limit of 200 ppm as well as NO 2 , SO 2 and O 3 (in the UV-visible) in 2006, 12 2000 13 and 2008 14 with limits of detection of 5 ppm, 10 ppm and 500 ppm, respectively. More recent work performed by Hodgkinson et al 15,16 has enabled the realisation of spectroscopic sensor for CH 4 (at 1.65 µm) with limits of detection of 75 ppm and 0.4 ppm for a sphere diameter of 50 mm using direct scan and 100 mm using wavelength modulation spectroscopy, respectively.…”
Section: Introductionmentioning
confidence: 99%