Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | tert-BUTYL CHLORIDE | HCID 10486 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Styrene-butadiene-styrene | HCID 22280236 | — |
Reaction Steps
4800 g of cyclohexane was placed in a 10 l autoclave reactor, followed by the addition of 11 g of tetrahydrofuran, 124 g of styrene monomer and 16 mmol of n-butyl lithium for 30-minute polymerization. Then, 552 g of 1,3-butadiene monomer were added to the reactor for another polymerization for 1 hour. Also, 124 g of styrene monomer were added for further polymerization for 30 minutes, followed by the addition of 1.5 g of t-butyl chloride to deactivate the terminal of polymer. Thus, a styrene-butadiene-styrene block copolymer, so obtained, had the following characteristics: 31.0% as a combined content of styrene (block styrene content: 30.0%), 38.5% as a combined 1,2 vinyl content of butadiene unit, and a number average molecular weight of about 50,000.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06410657B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-1204e18773a846a3bb6e020e8336b778 |
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| Source note | uspto-grants-2002_06 |
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