GB982514A - Recovery of resorcinol - Google Patents

Recovery of resorcinol

Info

Publication number
GB982514A
GB982514A GB4897763A GB4897763A GB982514A GB 982514 A GB982514 A GB 982514A GB 4897763 A GB4897763 A GB 4897763A GB 4897763 A GB4897763 A GB 4897763A GB 982514 A GB982514 A GB 982514A
Authority
GB
United Kingdom
Prior art keywords
resorcinol
range
product
cracking
vapour
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
GB4897763A
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.)
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
Distillers Co Yeast Ltd
Distillers Co Ltd
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 Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical Distillers Co Yeast Ltd
Publication of GB982514A publication Critical patent/GB982514A/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
    • 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
    • C07C37/50Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions decreasing the number of carbon atoms
    • C07C37/52Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions decreasing the number of carbon atoms by splitting polyaromatic compounds, e.g. polyphenolalkanes
    • 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
    • C07C37/685Processes comprising at least two steps in series

Landscapes

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

Abstract

Resorcinol is recovered from the product of acid cleavage of m-diisopropylbenzenedihydroperoxide by distilling the cleavage product to remove low-boiling materials, heating the resulting product containing resorcinol to vaporize substantially all of the products other than the high-boiling condensation products, cracking the residual liquid mixture under reduced pressure and with the aid of steam stripping to vaporize further quantities of resorcinol, condensing the combined products of the vaporizer and the cracking process, and recovering resorcinol therefrom. The vaporization may be effected at a temperature in the range from 200 DEG to 250 DEG C., while the cracking may be effected in the range from 200 DEG to 280 DEG C., preferably at less than 500 mm. Hg, and particularly in the range from 50 to 250 DEG mm. Hg. Preferably the feed to the cracker is maintained above pH3 and the vapour phase before condensation is in the pH range from 4 to 7. In an example, a product obtained by the distillation of the cleavage product to remove low-boiling constituents is fed through <PICT:0982514/C2/1> 1 to vaporizer 2 in which all the uncombined resorcinol and water are vaporized; the vapour and residue is fed to column 4, the vapour passing overhead via 8 and the liquid residue to cracker 5 where it is thermally cracked while steam enters at 6 to drive off the vapours, and tar is removed at 7; the combined vapours from column 4 pass into condenser 9 and are cooled directly by water sprayed through 10; liquid resorcinol flows via 11 to vacuum receiver 12 into which flows water obtained by condensing in 14 any vaporized cooling water; toluene is added at 17 to remove phenolic substances and the mixture is taken off via 18 for separation of the resorcinol phase.
GB4897763A 1963-01-19 1963-12-11 Recovery of resorcinol Expired GB982514A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DESC032616 1963-01-19

Publications (1)

Publication Number Publication Date
GB982514A true GB982514A (en) 1965-02-03

Family

ID=7432505

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4897763A Expired GB982514A (en) 1963-01-19 1963-12-11 Recovery of resorcinol

Country Status (6)

Country Link
AT (1) AT248418B (en)
BE (1) BE642717A (en)
FR (1) FR1384992A (en)
GB (1) GB982514A (en)
LU (1) LU45236A1 (en)
NL (1) NL6400270A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4192958A (en) * 1977-09-30 1980-03-11 Mitsui Petrochemical Industries Ltd. Method for recovering resorcinol
JPS55130930A (en) * 1979-03-30 1980-10-11 Sumitomo Chem Co Ltd Recovery of dihydric phenol
US4283567A (en) * 1978-12-20 1981-08-11 Mitsui Petrochemical Industries Ltd. Method for recovering resorcinol
US4339614A (en) * 1980-03-14 1982-07-13 Pcuk Produits Chimiques Ugine Kuhlmann Superacid catalyzed preparation of resorcinol from meta-isopropylphenol

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117447310A (en) * 2023-10-25 2024-01-26 青岛科技大学 Separation method of reaction product liquid for preparing benzenediol by phenol hydroxylation

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4192958A (en) * 1977-09-30 1980-03-11 Mitsui Petrochemical Industries Ltd. Method for recovering resorcinol
US4283567A (en) * 1978-12-20 1981-08-11 Mitsui Petrochemical Industries Ltd. Method for recovering resorcinol
JPS55130930A (en) * 1979-03-30 1980-10-11 Sumitomo Chem Co Ltd Recovery of dihydric phenol
JPS6241489B2 (en) * 1979-03-30 1987-09-03 Sumitomo Chemical Co
US4339614A (en) * 1980-03-14 1982-07-13 Pcuk Produits Chimiques Ugine Kuhlmann Superacid catalyzed preparation of resorcinol from meta-isopropylphenol

Also Published As

Publication number Publication date
AT248418B (en) 1966-07-25
BE642717A (en)
NL6400270A (en) 1964-07-20
FR1384992A (en) 1965-01-08
LU45236A1 (en) 1964-03-17

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