GB970945A - Process for neutralising acidic acetone-phenol mixtures - Google Patents

Process for neutralising acidic acetone-phenol mixtures

Info

Publication number
GB970945A
GB970945A GB3401161A GB3401161A GB970945A GB 970945 A GB970945 A GB 970945A GB 3401161 A GB3401161 A GB 3401161A GB 3401161 A GB3401161 A GB 3401161A GB 970945 A GB970945 A GB 970945A
Authority
GB
United Kingdom
Prior art keywords
resin
acetone
water
cumene
hydrolysate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB3401161A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Societa Italiana Resine SpA SIR
Original Assignee
Societa Italiana Resine SpA SIR
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Societa Italiana Resine SpA SIR filed Critical Societa Italiana Resine SpA SIR
Publication of GB970945A publication Critical patent/GB970945A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C37/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
    • C07C37/68Purification; separation; Use of additives, e.g. for stabilisation
    • C07C37/70Purification; separation; Use of additives, e.g. for stabilisation by physical treatment
    • C07C37/82Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by solid-liquid treatment; by chemisorption
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C37/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
    • C07C37/08Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by decomposition of hydroperoxides, e.g. cumene hydroperoxide
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/51Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C07C45/53Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition of hydroperoxides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/78Separation; Purification; Stabilisation; Use of additives
    • C07C45/79Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Solutions containing at least 25% by weight of cumene peroxide obtained from the acid hydrolysis of cumene hydroperoxide in admixture with cumene, and possibly side products of the oxidation of cumene by air or molecular oxygen, are neutralised by passing over an anion exchange resin, preferably phenolic-base resins having a secondary amino or tertiary amino functional group. A fixed bed of resin in a column is employed. The resin is first brought to its hydroxyl state by washing with dilute NaOH, and then with distilled water, to remove excess NaOH. When the water retained by the resin has been fully displaced by acetone the supply of acidic hydrolysate is started, and stopped when the resin is spent. The residual partly neutralised hydrolysate in the resin is displaced by acetone and added to the acidic hydrolysate to be neutralised in the next run. Upon completion of this displacement, the acetone is displaced in turn by distilled water and the resin then regenerated using NaOH solution. The cycle can then be repeated. In modifications of the process, after regenerating the resin with NaOH and washing with water, instead of displacing the water with acetone, the water is discharged by draining. Water absorbed by the resin is removed with warm air and the supply of acid hydrolysate then started. Upon completion of the cycle, instead of displacing the partly neutralised hydrolysate with acetone, the mixture is drained from the resin with the assistance of compressed air. The resin is then washed by flooding it from the bottom with acetone and subsequently water. Washing with water and regeneration are carried out as before. In examples "Duolite" A7 and A2 resins (Registered Trade Marks) are utilised in the process and its modifications to neutralise a phenol/acetone mixture containing about 22% of a mixture of cumene and side-products and 0.2% sulphuric acid.
GB3401161A 1960-11-12 1961-09-22 Process for neutralising acidic acetone-phenol mixtures Expired GB970945A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT1967660 1960-11-12

Publications (1)

Publication Number Publication Date
GB970945A true GB970945A (en) 1964-09-23

Family

ID=11160302

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3401161A Expired GB970945A (en) 1960-11-12 1961-09-22 Process for neutralising acidic acetone-phenol mixtures

Country Status (1)

Country Link
GB (1) GB970945A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003076381A1 (en) * 2002-03-14 2003-09-18 Eurotecnica Development & Licensing S.P.A. Process for the synthesis of cumene hydroperoxide
EP1411040A1 (en) * 2002-10-15 2004-04-21 Kellogg Brown & Root, Inc. Low sodium cleavage product in phenol production
CN105646156A (en) * 2010-09-14 2016-06-08 埃克森美孚化学专利公司 Method for preparing phenol

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003076381A1 (en) * 2002-03-14 2003-09-18 Eurotecnica Development & Licensing S.P.A. Process for the synthesis of cumene hydroperoxide
US7335797B2 (en) 2002-03-14 2008-02-26 Eurotechnica Development & Licensing S.P.A. Process for the synthesis of cumene hydroperoxide
EP1411040A1 (en) * 2002-10-15 2004-04-21 Kellogg Brown & Root, Inc. Low sodium cleavage product in phenol production
US6825387B2 (en) 2002-10-15 2004-11-30 Kellogg Brown & Root, Inc. Low sodium cleavage product
CN105646156A (en) * 2010-09-14 2016-06-08 埃克森美孚化学专利公司 Method for preparing phenol
EP3031792A1 (en) * 2010-09-14 2016-06-15 ExxonMobil Chemical Patents Inc. Processes for producing phenol
US9815759B2 (en) 2010-09-14 2017-11-14 Exxonmobil Chemical Patents Inc. Processes for producing phenol
CN105646156B (en) * 2010-09-14 2018-07-13 埃克森美孚化学专利公司 The method for being used to prepare phenol

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