Styrene → Benzene, ethenyl-, polymer with 1,3-butadiene

HRID 1076433Notes

Reaction equation

HRID 1076433 reaction equation
[CH2:1]=[CH:2][CH:3]=[CH2:4].[CH2:5]=[CH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.C(C1C=CC=CC=1C=C)=C.C([O-])(=O)CCCCCCC/C=C\CCCCCCCC.[K+].[O-]O.C(C1C=CC=CC=1C(C)C)(C)C.C(S([O-])=O)O.[Na+].S([O-])[O-].C=O.[Na+].[Na+]>[Fe].O>[CH2:1]=[CH:2][CH:3]=[CH2:4].[CH2:5]=[CH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1

Participants

10

Procedure

Into a stainless steel autoclave of 10-liter capacity having an agitator, there were charged 48 parts by weight of butadiene, 12 parts by weight of styrene, 0.6 part by weight of divinyl benzene, and 200 parts by weight of water containing therein 0.9 part by weight of potassium oleate as an emulsifier, 0.12 part by weight of diisopropyl benzene hydroperoxide as a polymerization initiator, and a very small amount of redox assistants such as iron, Rongalite (a trademark for sodium formaldehyde sulfoxylate), and so on, and the emulsion-polymerization was conducted at a temperature of 45°C for 16 hours to obtain a rubber latex of butadiene-styrene copolymer.

Sources & evidence

ORD record
ord-db5d79627bda4047bd351faa69712e8e
Source dataset
uspto-grants-1976_05
Patent number
US03956424

Reaction notes

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