関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Methanethiol | HCID 878 | — |
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Ethanethiol | HCID 6343 | — |
| 反応物 | Sulfur | HCID 5362487 | — |
| 生成物 | Dimethyl Sulfide | HCID 1068 | — |
| 生成物 | Ethyl sulfide | HCID 9609 | — |
| 生成物 | Ethyl methyl sulfide | HCID 12230 | — |
反応手順
To produce a sulfide, the sulfur compound reactant stream 10b can be a mercaptan, such as methanethiol (methyl mercaptan) or ethanethiol (ethyl mercaptan). Either one of these mercaptans can be reacted with methanol or ethanol as the alcohol feed stream 8b to produce 2-thiopropane (dimethyl sulfide), 1-(methylthio)ethane (methyl ethyl sulfide), or 1,1′-thiobisethane (diethyl sulfide), depending upon the selected sulfur compound reactant stream 10b and alcohol feed stream 8b. For example, methanethiol (methyl mercaptan) can be reacted with methanol, in the presence of the catalyst blend 5b of the present invention, to produce 2-thiopropane (dimethyl sulfide) or with ethanol to produce 1-(methylthio)ethane (methyl ethyl sulfide). As another example, ethanethiol (ethyl mercaptan) can be reacted with methanol to produce 1-(methylthio)ethane (methyl ethyl sulfide) or with ethanol to produce 1,1′-thiobisethane (diethyl sulfide). As shown in FIG. 3, the catalyst blend 5b includes a plurality of zones with each zone having a lower volumetric ratio of the alumina diluent B to the hydrotreating catalyst A than the previous zone.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07399893B2 |
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| 出典データセット | uspto-grants-2008_07 |
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| ORD ID | ord-d4465cdf039543f1bbf379bcdc8b34c4 |
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| 出典メモ | uspto-grants-2008_07 |
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