Styrene → Styrene-butadiene-styrene
Reaction equation
[CH:1]([Li])([CH2:3][CH3:4])[CH3:2].[CH2:6]=[CH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.O1CCCC1.C=CC=C>C1CCCCC1>[CH2:6]=[CH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[CH2:2]=[CH:1][CH:3]=[CH2:4].[CH2:6]=[CH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
In a 200 L pressure-resistant vessel filled with dry nitrogen, 75 kg of cyclohexane as a solvent and 45 g of sec-butyllithium as a polymerization initiator were added and, subsequently, 3.4 kg of styrene was added. After polymerization at 50° C., 0.21 kg of tetrahydrofuran as a Lewis base was added and, subsequently, 33.2 kg of butadiene and 3.4 kg of styrene were added in this order. When polymerization was carried out, a triblock copolymer of styrene-butadiene-styrene type was obtained. The block copolymer had a branching degree (α) of 0.150. The block copolymer obtained was subjected to hydrogenation at a hydrogen pressure of 2 MPa and a reaction temperature of 100° C. in cyclohexane using Pd/C as a catalyst, yielding a styrene-hydrogenated butadiene-styrene block copolymer (SEBS). The resulting block copolymer had a weight average molecular weight of 100900, a styrene content of 17% by weight, and a ratio of hydrogenation of 95 mol %.
Workup
- customAfter polymerization at 50° C.
- customWhen polymerization
Sources & evidence
- ORD record
- ord-441d848f6fd847ff973e0143f80255e7
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07109272B2
Reaction notes
Loading…