Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Styrene-butadiene-styrene | HCID 22280236 | — |
Reaction Steps
Into a reaction vessel with a stirrer, 50 kg of cyclohexane, 1,750 g of well dehydrated styrene and 210 g of sec-butyl lithium (10% by weight, cyclohexane solution) were charged to carry out polymerization at 60° C. for 60 minutes. Next, 250 g of tetrahydrofuran was added and 6,500 g of butadiene was also added to carry out polymerization for 60 minutes. Then, 1,750 g of styrene was further added to carry out polymerization for 60 minutes. Thereafter, methanol was added to terminate the reaction. Thus, a styrene-butadiene-styrene type block copolymer was obtained. The block copolymer obtained was subjected to hydrogenation under the same conditions as in Reference Example 1 to give a hydrogenated product of the block copolymer (hereinafter simply referred to as "SEBS"). The SEBS thus obtained had a number average molecular weight of 76,100 and a styrene content of 35% by weight, where the ratio of hydrogenation was 98.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05693711 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-de1b32a6765d4cef91aa05e28d2eff56 |
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| Source note | uspto-grants-1997_12 |
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