GB835569A - Manufacture of phenol - Google Patents

Manufacture of phenol

Info

Publication number
GB835569A
GB835569A GB3720456A GB3720456A GB835569A GB 835569 A GB835569 A GB 835569A GB 3720456 A GB3720456 A GB 3720456A GB 3720456 A GB3720456 A GB 3720456A GB 835569 A GB835569 A GB 835569A
Authority
GB
United Kingdom
Prior art keywords
sodium sulphite
sodium
solution
phenol
sulphite
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
GB3720456A
Inventor
Ernest Clifford Holdsworth
David William Milner
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.)
YORKSHIRE TAR DISTILLERS Ltd
Original Assignee
YORKSHIRE TAR DISTILLERS 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 YORKSHIRE TAR DISTILLERS Ltd filed Critical YORKSHIRE TAR DISTILLERS Ltd
Priority to GB3720456A priority Critical patent/GB835569A/en
Publication of GB835569A publication Critical patent/GB835569A/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
    • C07C37/01Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis
    • C07C37/04Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis by substitution of SO3H groups or a derivative thereof

Abstract

Pure solid sodium sulphite is obtained as a by-product in a process for manufacturing phenol in which the product from the quenching of a sodium hydroxide fusion of benzene sulphonic acid with water or sodium sulphite or bisulphite solution, is partially or completely neutralized prior to the separation of the sodium sulphite, by the addition of a solution of sodium bisulphite or by the introduction of sulphur dioxide under conditions resulting in the precipitation of solid sodium sulphite. The quenched fusion mass may be completely neutralized, semi-neutralized, i.e. 75-100%, or partially neutralized, i.e. 40-75%, and in each case solid sodium sulphite may be centrifuged off from the phenol layer and the aqueous solution of sodium sulphite which may be used as such for quenching or converted to bisulphite solution for neutralizing. The sodium sulphite obtained is a mixture of that formed in the fusion reaction and a more pure sample formed during the neutralization and comparative analyses are given of sodium sulphite obtained according to the invention and a sample derived from the fusion operation without prior bisulphite treatment of the sodium phenate. Flow sheets showing complete and partial neutralization and phenol finishing are given together with a detailed example.ALSO:Phenol is manufactured by a process in which the product from the quenching of a sodium hydroxide fusion of benzene sulphonic acid with water or sodium sulphide or bisulphite solution, is partially or completely neutralized prior to the separation of the sodium sulphite, by the addition of a solution of sodium bisulphite or by the introduction of sulphur dioxide under conditions resulting in the precipitation of solid sodium sulphite. The slurry of sodium phenate and sodium sulphite resulting from the quenching of the fused mass may be completely neutralized with bisulphite solution or by gassing with sulphur dioxide to give three layers, the top being wet phenol, the middle being sodium sulphite solution and the lower solid sodium sulphite. The phenol layer is removed for finishing and the residue centrifuged to give solid sodium sulphite (a mixture of that formed in the fusion reaction and a more pure sample formed in the neutralization and sodium sulphite solution. The quenched fusion mass may also be semi-neutralized, i.e. to an extent of 75 to 100%. Three layers are again obtained but the phenol layer must be treated with bisulphite solution before finishing and the sodium sulphite solution obtained contains some sodium phenate which may be recycled. Alternatively the quenched fusion mass may be partially neutralized, i.e. to an extent of 40 to 75%, preferably about 50%. In this case further sodium sulphite is precipitated but no phenol layer separates. The mixture is centrifuged to separate the solid sulphite from the solution which is then completely neutralized and the phenol layer separated from the aqueous sodium sulphite solution, no solid being precipitated in the second step. The phenol layer separated from the neutralization contains in addition to water, sodium sulphite and sodium benzene sulphonate which may be removed by extraction with water and recycled to the fusion stage. The phenol may then be purified by distillation. The solid sodium sulphite is recovered as a by-product and the sodium sulphite solution used in the quenching stage or converted to bisulphite solution by gassing with sulphur dioxide and used in the neutralization. Flow sheets are given of the complete neutralization, partial neutralization and phenol finishing stages and a detailed example of the whole process is given.
GB3720456A 1956-12-05 1956-12-05 Manufacture of phenol Expired GB835569A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3720456A GB835569A (en) 1956-12-05 1956-12-05 Manufacture of phenol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3720456A GB835569A (en) 1956-12-05 1956-12-05 Manufacture of phenol

Publications (1)

Publication Number Publication Date
GB835569A true GB835569A (en) 1960-05-25

Family

ID=10394627

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3720456A Expired GB835569A (en) 1956-12-05 1956-12-05 Manufacture of phenol

Country Status (1)

Country Link
GB (1) GB835569A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113998824A (en) * 2021-10-11 2022-02-01 金能科技股份有限公司 Production method and equipment for reducing salt content and solid waste of p-methylphenol

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113998824A (en) * 2021-10-11 2022-02-01 金能科技股份有限公司 Production method and equipment for reducing salt content and solid waste of p-methylphenol
CN113998824B (en) * 2021-10-11 2023-08-29 金能科技股份有限公司 Production method and equipment for reducing salt content and solid waste of p-methylphenol

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