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HRID 66451作成日:2026年10月25日

Azobisisobutyronitrile → Butadiene maleic acid

https://huagongshe.com/reaction/66451

反応式

関与物質

役割名称HCID仕込み量
反応物AzobisisobutyronitrileHCID 6547—
反応物1,3-ButadieneHCID 7845—
反応物Maleic AnhydrideHCID 7923—
反応物1-DodecanethiolHCID 8195—
反応物Sodium HydroxideHCID 14798—
反応物SulfurHCID 5362487—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
生成物Butadiene maleic acidHCID 86738509—

反応手順

A polymerization was carried out at 70° C. for 6 hrs. using 54.1 g. of butadiene, 98.1 g. of maleic anhydride, 1.7 g. of azobisisobutyronitrile and 36.0 g. of n-dodecylmercaptan in 750 cc. of acetone. There was obtained 61.0 g. of a white copolymer with an intrinsic viscosity of 0.08. Proportion of the end dodecylthio group in the copolymer was found by the elementary analysis for sulfur to be 5.4%. A reaction was carried out at 80° C. for 1 hr. using 16.1 g. of the copolymer, 6.0 g. of sodium hydroxide and 139 g. of water to give an aqueous solution of a butadiene-maleic acid copolymer sodium salt containing end dodecylthio groups. A composition identical in composition with the composition of Example 2 was prepared using the above-prepared aqueous solution, an aqueous calcium chloride solution at a concentration of 0.1 M/l, an aqueous solution of sodium lauryl sulfate at a concentration of 30% and water to which THPA was added in the same amount as that of the copolymer salt. Aqueous gel obtained from the composition was slower in rate of the gelation and lower in strength of the gel as compared with the aqueous gel of Example 2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04342665
出典データセットuspto-grants-1982_08
ORD IDord-612335c55f524cf5863308144335608a
出典メモuspto-grants-1982_08