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HRID 531387作成日:2026年10月26日

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

https://huagongshe.com/reaction/531387

反応式

関与物質

役割名称HCID仕込み量
反応物OxygenHCID 977—
反応物4-tert-ButylcatecholHCID 7381—
反応物1,3-ButadieneHCID 7845—
溶媒WaterHCID 962—
生成物Benzene, ethenyl-, polymer with 1,3-butadieneHCID 62697—

反応手順

A pressure-resistant glass bottle, specifically an empty bottle for carbonated drink was used as a reactor; 60 g of ion-exchanged water was charged in this glass bottle; and dissolved oxygen was removed with a nitrogen gas. This glass bottle was cooled in an iced water bath; the emulsifier that is the invention product or comparative product and polyfunctional monomers shown in Table 4 were added; 0.12 g of a naphthalenesulfonic acid formalin condensate, 0.12 g of sodium carbonate, and 0.12 g of dodecyl mercaptan were added; and the glass bottle was temporarily plugged with a rubber stopper. This glass bottle was lightly manually shaken to make the contents uniform and then opened; 20 g of styrene and 0.12 g of potassium persulfate were charged; and the glass bottle was again temporarily plugged with a rubber stopper and allowed to stand for cooling in an iced water bath. Subsequently, butadiene was introduced from a butadiene cylinder into a graduated sample collecting tube in a methanol dry ice bath and liquefied. And 20 g of the liquefied butadiene was weighed out and charged in the glass bottle by using a stop cock-equipped syringe; and immediately after charging, a prescribed metal-made crown was covered and capped, thereby preparing a bottle polymerization reactor. Subsequently, the capped glass bottle was vigorously shaken, thereby making the content liquid in the glass bottle in an emulsified state. Subsequently, the glass bottle was set in a holder within a rotary polymerization tank for bottle polymerization adjusted at a water temperature of 50° C., polymerization was conducted for 20 hours at a rotation number of 50 rpm, thereby conducting emulsion polymerization by the bottle polymerization method. The glass bottle was then put in an iced water bath and cooled. Then, after opening the glass bottle, 0.12 g of p-tert-butyl catechol was added, and unreacted butadiene was vaporized and distilled off by means of bubbling of a nitrogen gas within a draft, thereby obtaining a polymer dispersion.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09353195B2
出典データセットuspto-grants-2016_05
ORD IDord-ba5af217e33b4adeb30ed139d1f11d9c
出典メモuspto-grants-2016_05