Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene | HCID 6325 | — |
| Reactant | Acetylene | HCID 6326 | — |
| Reactant | Vinyl Chloride | HCID 6338 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | Ethane | HCID 6324 | — |
| Product | Chloroethane | HCID 6337 | — |
| Product | Butane | HCID 7843 | — |
Reaction Steps
The reactor was packed to a bed height of 1.50 m with hydrogenation catalyst consisting of gamma-aluminum oxide with a specific surface of 120 m2 /g and doped with 0.1 wt % of palladium. The catalyst was used in the form of tablets measuring 3 mm×3 mm. In reactor 4, ethylene, vinyl chloride, unsaturated C4 -hydrocarbons and optionally acetylene were hydrogenated to form mainly ethane, ethyl chloride and n-butane. The superficial gas velocity calculated with respect to the internal reactor cross-section under reaction conditions is approx. 0.25 msec-1 and the contact time was calculated as approx. 6 seconds. Since the reactor was adiabatically operated and the hydrogenation proceeds weakly exothermically, the gas mixture left reactor 4 at a temperature of approx. 140° C. The gas mixture was passed to water cooler 6 by line 5 where it was cooled to 30° C. Then, the gas mixture flew to the suction side of compressor 7 where it was compressed from approx. 7.5 bar (absolute) to 14 bar (absolute). After the compressed gas was cooled to approx. 30° C. in water cooler 8 and further supercooled by heat exchange with hydrogen chloride gas of approx. -24° C. from the head of the rectifying column 10 in counter-current heat exchanger 9, the gaseous hydrogen chloride flowed through line 5 into column 10, while any produced condensate flowed from water cooler 8 and counter-current heat exchanger 9 through lines 11 and 12 to receiving tank 25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04839153 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-14dfed0fa6de4e74ac3f4d77013c4a76 |
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| Source note | uspto-grants-1989_06 |
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