TY - JOUR
T1 - Conversion of emitted dimethyl sulfide into eco-friendly species using low-temperature atmospheric argon micro-plasma system
AU - Chen, Hsin Hung
AU - Weng, Chih Chiang
AU - Liao, Jiunn Der
AU - Whang, Liang Ming
AU - Kang, Wei Hung
N1 - Funding Information:
This work was financially supported by Chi-Mei Optoelectronics (under grant number 97S062 ) and National Science Council of Taiwan (under grant numbers 99-2221-E-006-013-MY3 , 99-2911-I-006-013- , and 100-2911-I-006-008- ).
PY - 2012/1/30
Y1 - 2012/1/30
N2 - A custom-made atmospheric argon micro-plasma system was employed to dissociate dimethyl sulfide (DMS) into a non-foul-smelling species. The proposed system takes the advantages of low energy requirement and non-thermal process with a constant flow rate at ambient condition. In the experiments, the compositions of DMS/argon plasma, the residual gaseous phases, and solid precipitates were respectively characterized using an optical emission spectrometer, various gas-phase analyzers, and X-ray photoemission spectroscopy. For 400ppm DMS introduced into argon plasma with two pairs of electrodes (90W), a complete decomposition of DMS was achieved; the DMS became converted into excited species such as C*, C 2*, H*, and CH*. When gaseous products were taken away from the treatment area, the excited species tended to recombine and form stable compounds or species, which formed as solid particles and gaseous phases. The solid deposition was likely formed by the agglomeration of C-, H-, and S-containing species that became deposited on the quartz inner tube. For the residual gaseous phases, low-molecular-weight segments mostly recombined into relatively thermodynamic stable species, such as hydrogen, hydrogen sulfide, and carbon disulfide. The dissociation mechanism and treatment efficiency are discussed, and a treatment of converting DMS into H 2-, CS 2-, and H 2S-dominant by-products is proposed.
AB - A custom-made atmospheric argon micro-plasma system was employed to dissociate dimethyl sulfide (DMS) into a non-foul-smelling species. The proposed system takes the advantages of low energy requirement and non-thermal process with a constant flow rate at ambient condition. In the experiments, the compositions of DMS/argon plasma, the residual gaseous phases, and solid precipitates were respectively characterized using an optical emission spectrometer, various gas-phase analyzers, and X-ray photoemission spectroscopy. For 400ppm DMS introduced into argon plasma with two pairs of electrodes (90W), a complete decomposition of DMS was achieved; the DMS became converted into excited species such as C*, C 2*, H*, and CH*. When gaseous products were taken away from the treatment area, the excited species tended to recombine and form stable compounds or species, which formed as solid particles and gaseous phases. The solid deposition was likely formed by the agglomeration of C-, H-, and S-containing species that became deposited on the quartz inner tube. For the residual gaseous phases, low-molecular-weight segments mostly recombined into relatively thermodynamic stable species, such as hydrogen, hydrogen sulfide, and carbon disulfide. The dissociation mechanism and treatment efficiency are discussed, and a treatment of converting DMS into H 2-, CS 2-, and H 2S-dominant by-products is proposed.
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U2 - 10.1016/j.jhazmat.2011.11.064
DO - 10.1016/j.jhazmat.2011.11.064
M3 - Article
C2 - 22172460
AN - SCOPUS:84855344835
SN - 0304-3894
VL - 201-202
SP - 185
EP - 192
JO - Journal of Hazardous Materials
JF - Journal of Hazardous Materials
ER -