Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | 68953-70-8 | HCID 160054 | — |
| Reactant | HCID 21703154 | HCID 21703154 | — |
| Product | Triethanolamine | HCID 7618 | — |
| Product | Diethanolamine | HCID 8113 | — |
Reaction Steps
The reaction was carried out by use of the apparatus shown in FIG. 5. A stainless steel tube having an inner diameter of 15 mm, a length of 400 mm, a heater wound thereon for compensating the heat radiation, and a heat-insulation was used as a reactor 501. Within the reactor 501, a protection tube where a thermocouple could be inserted to measure the temperature profile of a fixed catalytic layer, was installed. Into the reactor 501 was packed 50 cm3 of catalyst A, and the raw material (the molar ratio of ammonia/ethylene oxide: 8/1) heated to 60° C. through a pre-heater 502 was fed at 5 hr−1 (LHSV), to carry out the reaction. The reaction pressure was 10 MPa, and the reaction was in a gas-liquid mixing phase. Though the temperature increased up to 150° C. by the heat of reaction over the length of about 100 mm from the inlet at the initial stage, the temperature came to have a profile barely rising to nearly 150° C. after 200 hrs near the outlet of the catalytic layer. As a result, a reduction in catalytic activity was observed. The results obtained are as follows: the conversion of ethylene oxide was 100%; and the ratio of each component in the produced ethanolamines was: monoethanolamine/diethanolamine/triethanolamine=51/46/3. Diethanolamine was produced at a high selectivity while a small amount of triethanolamine was produced.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06559342B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-fba3b2a4933e4f01950ea81e631c8130 |
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| Source note | uspto-grants-2003_05 |
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