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

HRID 1076432Notes

Reaction equation

HRID 1076432 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 42 parts by weight of butadiene, 10 parts by weight of styrene, 0.14 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, 0.11 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 of sodium formaldehyde sulfoxylate), and so on, and the emulsion-polymerization was conducted at a temperature of 45°C for 17 hours to obtain a rubber latex of butadiene-styrene copolymer.

Sources & evidence

ORD record
ord-59a9a15270ae40d48895ccfcae4f86c7
Source dataset
uspto-grants-1976_05
Patent number
US03956424

Reaction notes

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