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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 487511생성일: 2026년 10월 24일

Methane → Resorcinol

https://huagongshe.com/ko/reaction/487511

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물Hydrochloric AcidHCID 313—
반응물WaterHCID 962—
반응물StyreneHCID 7501—
반응물2-Ethylhexyl acrylateHCID 7636—
반응물Phenyl isocyanateHCID 7672—
반응물Lauroyl peroxideHCID 7773—
반응물Toluene 2,4-DiisocyanateHCID 11443—
반응물1-Methyl-4-nitroimidazoleHCID 18209—
반응물Tricalcium PhosphateHCID 24456—
반응물1,2-DiethenylbenzeneHCID 66666—
용매tert-ButanolHCID 6386—
생성물ResorcinolHCID 5054—
생성물DabcoHCID 9237—
생성물3-AminophenolHCID 11568—

반응 단계

40 parts by weight of carbon black grafted with styrene "GP-E-3" (manufactured by Ryoyu Kogyo K. K.), which contains 40% by weight of styrene monomer, 30% by weight of polystyrene and 30% by weight of grafted carbon black, 1.5 parts by weight of charge control agent of negative charging type 3-methyl-5-nitroimidazole, 4.5 parts by weight of lauroyl peroxide, 9.0 parts by weight of tolylene diisocyanate "Coronate T-100" (mfd. by Nippon Polyurethane Industry Co., Ltd.) and 0.5 part by weight of phenyl isocyanate were added to a mixture of 50 parts by weight of styrene with 35 parts by weight of 2-ethylhexyl acrylate and 0.9 part by weight of divinylbenzene to prepare a polymerizable composition. The polymerizable composition was added to 800 g of a 4 wt. % solution of calcium phosphate in an aqueous colloid previously prepared in a 2-l separable glass flask in such an amount that the concentration of the polymerizable composition became 30 % by weight based on the total of the aqueous colloid solution and the polymerizable composition. The mixture was dispersed and emulsified on a TK Homomixer mfd. by Tokushu Kika Kogyo Co., Ltd. at 10,000 rpm at 5° C. for 2 min. A four neck glass lid was placed on the flask and fitted with a reflux condenser, a thermometer, a dropping funnel having a nitrogen-inlet tube and a stainless steel stirring rod. The flask was placed in an electric mantle. A mixed solution of 24.0 g of resorcinol, 3.0 g of m-aminophenol, 2.2 g of t-butyl alcohol, 0.5 g of 1,4-diazabicyclo[2.2.2]-octane and 40 g of deionized water was prepared and added dropwise into the flask through the dropping funnel while stirring over a period of 30 min. Then the temperature was elevated to 85° C. while continuing the stirring under nitrogen and the reaction was conducted for 10 h. After cooling the reaction mixture, the dispersant was dissolved by adding 10% aqueous hydrochloric acid solution, and the mixture was filtered. The residue was washed with water, dried at 45° C. for 12 hr under a reduced pressure of 20 mmHg, and classified by means of an air classifier to give an encapsulated toner having an average particle diameter of 9 μm wherein the shell comprises a resin having thermally dissociable urethane bonds. The glass transition point of the resin in the core material of the encapsulated toner and the softening point of the encapsulated toner were 32.0° C. and 129.5° C., respectively.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05294490
출처 데이터셋uspto-grants-1994_03
ORD IDord-745390f1ad1346cabf82b62a14670b2a
출처 메모uspto-grants-1994_03