Process for preparing beta,beta'-bis-(3,5-dichloro-4-hydroxyphenyl)-propane
    1.
    发明授权
    Process for preparing beta,beta'-bis-(3,5-dichloro-4-hydroxyphenyl)-propane 失效
    制备BETA,BET-BIS-(3,5-二氯-4-羟基苯基)丙酸的方法

    公开(公告)号:US3839466A

    公开(公告)日:1974-10-01

    申请号:US21111971

    申请日:1971-12-22

    CPC classification number: C07C37/62 C07C39/367

    Abstract: 1. A PROCESS FOR THE MANUFACTUREOF BETA, BETA''-BIS-(3, 5-DICHLORO-4 - HYDROXYPHENYL)-PROPANE COMPRISING THE STEPS OF ADDING GASEOUS CHLORINE TO BETA,BETA''-BIS-(4-HYDROXYPHENYL)-PROPANE WHICH IS DISSOLVED IN METHANO, AT WORKING TEMPERATURES NOT EXCEEDING 20*C. AND IN THE PRESENCE OF (A) AT LEAST ONE SUBSTANCE HAVING A CATALYTIC EFFECT ON THE CHLORINATION REACTION, SAID SUBSTANCE BEING A METAL CHLORIDE SELECTED FROM THE GROUP CONSISTING OF IRON AND COPPER CHLORIDES, AND (B) AT LEAST ONE SUBSTANCE HAVING AN INHIBITING EFFECT ON FREE RADICAL REACTIONS, SAID SUBSTANCE BEING AN ANTIOXIDIZING AGENT SELECTED FROM THE GROUP CONSISTING OF CRESOLS, THIOCRESOLS, P-TERBUTYL-CATECHOL, HYDROQUINONE AND THE PRODUCTS OF CONDENSATION OF CROTONALDEHYDE WITH 3-METHYL-6-TERBUTYLPHENOL, CONTINUING SAIDCHLORIDE ADDITION UP TO A QUANTITY AT LEAST EQUAL TO THE STOICHIOMETRIC QUANTITY FOR THE CHLORINATION REACTION, AND RECOVERING BETA, BETA''-BIS - (3,5-DICHLORO - 4-HYDROXYPHENYL)-PROPANE FROM THE PRODUCTS OF THE CHLORINATION REACTION.

    Process of separating aromatic hydrocarbons from hydrocarbon mixtures
    5.
    发明授权
    Process of separating aromatic hydrocarbons from hydrocarbon mixtures 失效
    从油气混合物分离芳香烃的方法

    公开(公告)号:US3725257A

    公开(公告)日:1973-04-03

    申请号:US3725257D

    申请日:1971-05-04

    CPC classification number: C10G21/00 B01D11/0488 C07C7/10 Y10S585/932 C07C15/00

    Abstract: AROMATIC HYDROCARBONS ARE SEPARATED FROM A MIXTURE OF LIQUID HYDROCARBONS. THE MIXTURE OF LIQUID HYDROCARBONS IS EXTRACTED IN THE LIQUID PHASE IN AN EXTRACTION ZONE AT A TEMPERATURE FROM ABOUT 40*C. TO AOUT 80*C. WITH ETHYLENEDIAINE SOLVENT HAVING A WATER CONTENT OF FROM 00% TO 20% BY WEIGHT TO FORM AN EXTRACTED PHASE AND A RAFFINATE PHASE. THE EXTRACTED PHASE COMPRISES PREDOMINANTLY AROMATIC HYDROCARBONS, SOLVENT AND A MINOR AMOUNT OF NON-AROMATIC HYDROCARBONS. THE RAFFINATE PHASE COMPRISES PREDOMINANTLY NON-AROMATIC HYDROCARBONS. THE EXTRACTED PHASE AND THE RAFFINATE PHASE ARE SEPARATELY COLLECTED. THE EXTRACTED PHASE IS COLLED TO A TEMPERATURE AT LEAST 300*C. LOWER THAN THE TEMPERATURE OF THE EXTRACTION STEP AND THEN SEPARATED INTO A HEAVIER SOLVENT CONTAINING PHASE AND ALIGHTER HYDROCARONS CONTAINING PHASE. THE NON-AROMATIC HYDROCARBONS IN THE LIGHTER HYDROCARBONS CONTAINING PHASE ARE SEPARATED A OVERHEAD PRODUCT BY MEANS OF EXTRACTIVE STRIPPING AT ATMOSPHERIC PRESSURE. THE AROMATIC HYDROCARBONS REMAIN IN THE RESIDUE OF THE EXTRACTIVE STRIPPING WHICH IS THEN SCRUBBED WITH WATER TO THEREBY OBTAIN AN AROMATIC HYDROCARBONS PHASE AND AN AQUEOUS ETHYLENEDIAMINE CONTAINING PHASE. THE AROMATIC HYDROCARBONS PHASE IS THEN RECTIFIED.

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