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Experimental studies on the ignition behavior of pure silane released into air
Authors:Hsiao-Yun Tsai  Sheng-Wei Wang  Sin-Ying Wu  Jenq-Renn Chen  Eugene Y Ngai  Kelvin Pai-Ping Huang
Institution:1. Department of Safety, Health and Environmental Engineering, 1 University Road, National Kaohsiung First University of Science & Technology, Yenchau, Kaohsiung 824, Taiwan;2. Chemically Speaking LLC, 26 Casper Berger Rd., Whitehouse Station, NJ 08889, USA;3. Air Products San Fu Co. Ltd., Chu Pei, Hsinchu, Taiwan;1. Department of Materials Science and Engineering, National Cheng Kung University, No. 1, University Road, Tainan City 701, Taiwan;2. Department of Materials Science, National University of Tainan, 33 Sec. 3, Shu-Lin St., Tainan 70005, Taiwan;3. Center for Micro/Nano Science and Technology, National Cheng Kung University, No. 1, University Road, Tainan City 701, Taiwan;4. Research Center for Energy Technology and Strategy, National Cheng Kung University, No. 1, University Road, Tainan City 701, Taiwan;5. Advanced Optoelectronic Technology Center, National Cheng Kung University, No. 1, University Road, Tainan City 701, Taiwan;1. National Engineering Research Center for Nanotechnology, 28 East Jiangchuan Road, Minhang District, Shanghai, CA 200241, PR China;2. School of Materials Science and Engineering, Shanghai JiaoTong University, 800 Dongchuan Road, Minhang District, Shanghai, CA 200240, PR China;1. Department of Physical Chemistry and Department “Science and Technology of Life, Light and Matter”, University of Rostock, Dr-Lorenz-Weg 1, D-18059 Rostock, Germany;2. Department of Physical Chemistry, Kazan Federal University, Kremlevskaya str. 18, 420008 Kazan, Russia
Abstract:Silane is a well known pyrophoric gas which normally ignites upon contact with air. However, a silane release from a pressure source may not always lead to prompt ignition and frequently the ignition occurs when the release is shutoff. In a confined space, significant quantities of silane can accumulate prior to autoignition leading to an explosion, causing significant damage. To date, the mechanism and condition of pure silane ignition upon release into air has not been completely explained. Thus there is a need for additional experimental investigations covering a wide range of release conditions to enable a full understanding of silane ignition and explosion characteristics.This work presents a series of tests that aims to uncover the precise condition for pure silane ignition upon release into air. Tests were performed for releases at controlled and steady velocities. Steady flow of silane to a burn box and nitrogen to the desired vent stub are first established through mass flow controllers. An electrically controlled four-way switching valve is used to switch the silane and nitrogen flow such that steady silane flow without acceleration to the vent stub can be established. With careful control of vent conditions, we are able to find a reproducible critical exit velocity for prompt ignition of steady silane releases for different vent diameters. If the releases are reduced to below the critical exit velocity, prompt ignition of silane release is ensured. Above this critical exit velocity, silane can be released indefinitely into air without any ignition. The critical exit velocity is found to vary with the vent diameter. This relationship between the critical exit velocity and the vent diameter suggests that the silane release without prompt ignition was most likely caused by quench of the reactive kernel from the scalar dissipation between the release gas and the ambient air. Analysis of locations where prompt ignition occurred from the clips from high speed video camera found that the most reactive ignition kernel occurs in the range when the ratio of volumetric flow rate of entrained air to the silane flow reaches 0.322 ± 0.076, which is equivalent to the most reactive silane concentration of 75.6% in air. The implications from these results are discussed with emphasis on the safety of silane supply systems and operation practices.
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