Stability of volatile sulfur compounds (VSCs) in sampling bags - impact of temperature

Volatile sulfur compounds (VSCs) are a major component of odorous emissions that can cause annoyance to local populations surrounding wastewater, waste management and agricultural practices. Odour collection and storage using sample bags can result in VSC losses due to sorption and leakage. Stabilit...

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Veröffentlicht in:Water science and technology : a journal of the International Association on Water Pollution Research. - 1986. - 68(2013), 8 vom: 25., Seite 1880-7
1. Verfasser: Le, H (VerfasserIn)
Weitere Verfasser: Sivret, E C, Parcsi, G, Stuetz, R M
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Water science and technology : a journal of the International Association on Water Pollution Research
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Disulfides Sulfhydryl Compounds Sulfides Sulfur Compounds ethylmethyl sulfide methylmercaptan 2X8406WW9I dimethyl trisulfide mehr... 3E691T3NL1 dimethyl disulfide 3P8D642K5E n-butyl mercaptan 77OY909F30 ethanethiol M439R54A1D dimethyl sulfide QS3J7O7L3U Hydrogen Sulfide YY9FVM7NSN
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245 1 0 |a Stability of volatile sulfur compounds (VSCs) in sampling bags - impact of temperature 
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520 |a Volatile sulfur compounds (VSCs) are a major component of odorous emissions that can cause annoyance to local populations surrounding wastewater, waste management and agricultural practices. Odour collection and storage using sample bags can result in VSC losses due to sorption and leakage. Stability within 72 hour storage of VSC samples in three sampling bag materials (Tedlar, Mylar, Nalophan) was studied at three temperatures: 5, 20, and 30 °C. The VSC samples consisted of hydrogen sulfide (H2S), methanethiol (MeSH), ethanethiol (EtSH), dimethyl sulfide (DMS), tert-butanethiol (t-BuSH), ethylmethyl sulfide (EMS), 1-butanethiol (1-BuSH), dimethyl disulfide (DMDS), diethyl disulfide (DEDS), and dimethyl trisulfide (DMTS). The results for H2S showed that higher loss trend was clearly observed (46-50% at 24 hours) at 30 °C compared to the loss at 5 °C or 20 °C (of up to 27% at 24 hours) in all three bag materials. The same phenomenon was obtained for other thiols with the relative recoveries after a 24 hour period of 76-78% at 30 °C and 80-93% at 5 and 20 °C for MeSH; 77-80% at 30 °C and 79-95% at 5 and 20 °C for EtSH; 87-89% at 30 °C and 82-98% at 5 and 20 °C for t-BuSH; 61-73% at 30 °C and 76-98% at 5 and 20 °C for 1-BuSH. Results for other sulfides and disulfides (DMS, EMS, DMDS, DEDS) indicated stable relative recoveries with little dependency on temperature (83-103% after 24 hours). DMTS had clear loss trends (with relative recoveries of 74-87% in the three bag types after 24 hours) but showed minor differences in relative recoveries at 5, 20, and 30 °C 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 7 |a Disulfides  |2 NLM 
650 7 |a Sulfhydryl Compounds  |2 NLM 
650 7 |a Sulfides  |2 NLM 
650 7 |a Sulfur Compounds  |2 NLM 
650 7 |a ethylmethyl sulfide  |2 NLM 
650 7 |a methylmercaptan  |2 NLM 
650 7 |a 2X8406WW9I  |2 NLM 
650 7 |a dimethyl trisulfide  |2 NLM 
650 7 |a 3E691T3NL1  |2 NLM 
650 7 |a dimethyl disulfide  |2 NLM 
650 7 |a 3P8D642K5E  |2 NLM 
650 7 |a n-butyl mercaptan  |2 NLM 
650 7 |a 77OY909F30  |2 NLM 
650 7 |a ethanethiol  |2 NLM 
650 7 |a M439R54A1D  |2 NLM 
650 7 |a dimethyl sulfide  |2 NLM 
650 7 |a QS3J7O7L3U  |2 NLM 
650 7 |a Hydrogen Sulfide  |2 NLM 
650 7 |a YY9FVM7NSN  |2 NLM 
700 1 |a Sivret, E C  |e verfasserin  |4 aut 
700 1 |a Parcsi, G  |e verfasserin  |4 aut 
700 1 |a Stuetz, R M  |e verfasserin  |4 aut 
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773 1 8 |g volume:68  |g year:2013  |g number:8  |g day:25  |g pages:1880-7 
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