GB687380A - Process for the purification of alcohols - Google Patents

Process for the purification of alcohols

Info

Publication number
GB687380A
GB687380A GB26148/50A GB2614850A GB687380A GB 687380 A GB687380 A GB 687380A GB 26148/50 A GB26148/50 A GB 26148/50A GB 2614850 A GB2614850 A GB 2614850A GB 687380 A GB687380 A GB 687380A
Authority
GB
United Kingdom
Prior art keywords
resin
resins
alcohol
anion
isopropanol
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
GB26148/50A
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.)
Bataafsche Petroleum Maatschappij NV
Original Assignee
Bataafsche Petroleum Maatschappij NV
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 Bataafsche Petroleum Maatschappij NV filed Critical Bataafsche Petroleum Maatschappij NV
Publication of GB687380A publication Critical patent/GB687380A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/74Separation; Purification; Use of additives, e.g. for stabilisation

Landscapes

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

Abstract

A process for the purification of an alcohol comprises bringing the alcohol which has received preliminary purification by fractional distillation into intimate contact with one or more ion exchange resins. Atmospheric temperature and pressure or elevated pressure and/or temperature may be employed. The alcohol may be mixed with the resin and filtered or passed through a bed of resin and the latter may be regenerated if an anion-exchange resin by flushing with a dilute solution of alkaline material such as sodium hydroxide, ammonium hydroxide or sodium carbonate whilst if a cation exchange resin by washing with a dilute solution, e.g. of hydrochloric or sulphuric acid. Anion- and cation-exchange resins may be used together or consecutively. Before or after the treatment the alcohol may be hydrogenated or refluxed with caustic alkali or permanganate. Isopropanol produced by the catalytic hydration of propylene may be fractionated, refluxed with potassium permanganate or other oxidizing agent such as sodium hypochlorite, hydrogen peroxide, sodium chromate or dichromate before treatment with the ion exchange resin. Representative anion-exchange resins are those of the phenol-formaldehyde-polyamine type, e.g. prepared by condensing phenols with formaldehyde to form intermediate water-soluble condensates containing methylol groups and further reacting with polyamines and heating, or the products obtained by condensation of aliphatic polyamines with polyhalogen derivatives of hydrocarbons. Representative of cation-exchange resins which may be used are phenol-formaldehyde sulphonic acid resins, a carboxylic acid resin and a sulphonated cross-linked polystyrene resin. Suitable commercial resins mentioned are "Amberlite" (Registered Trade Mark), IR-4B, IRA-400, IR-100, IRC-50, IR-120 and "Ionac" A-300, A-293-M, C-200 and C-212. In examples: (I) isopropanol, prepared by the hydration of propylene in the presence of a sulphuric acid catalyst is successively fractionated and passed through "Amberlite" IR-4B freshly regenerated with sodium hydroxide solution. A heart cut from the fractionated product is diluted with water and the odour compared with a solution of untreated isopropanol; (II) a similar process is carried out after treating the starting material with potassium permanganate. Similar runs were made using the other commercial resins mentioned. The process may be applied to other alcohols, e.g. ethanol or other aliphatic monohydric alcohols produced by catalytic hydration of olefines. Specification 489,173 is referred to.
GB26148/50A 1949-10-29 1950-10-26 Process for the purification of alcohols Expired GB687380A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US687380XA 1949-10-29 1949-10-29

Publications (1)

Publication Number Publication Date
GB687380A true GB687380A (en) 1953-02-11

Family

ID=22084403

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26148/50A Expired GB687380A (en) 1949-10-29 1950-10-26 Process for the purification of alcohols

Country Status (1)

Country Link
GB (1) GB687380A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0236981A1 (en) * 1986-03-12 1987-09-16 RWE-DEA Aktiengesellschaft für Mineraloel und Chemie Process for deodorization of isopropyl alcohol
EP0550183A1 (en) * 1991-12-16 1993-07-07 Texaco Chemical Inc. Purification of tertiary butyl alcohol
WO2023102727A1 (en) * 2021-12-07 2023-06-15 晶瑞电子材料股份有限公司 Method for producing ultra-high purity isopropanol by using resin purification method

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0236981A1 (en) * 1986-03-12 1987-09-16 RWE-DEA Aktiengesellschaft für Mineraloel und Chemie Process for deodorization of isopropyl alcohol
EP0550183A1 (en) * 1991-12-16 1993-07-07 Texaco Chemical Inc. Purification of tertiary butyl alcohol
WO2023102727A1 (en) * 2021-12-07 2023-06-15 晶瑞电子材料股份有限公司 Method for producing ultra-high purity isopropanol by using resin purification method

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