GB825475A - Process for the production of alkanolamines - Google Patents

Process for the production of alkanolamines

Info

Publication number
GB825475A
GB825475A GB1742558A GB1742558A GB825475A GB 825475 A GB825475 A GB 825475A GB 1742558 A GB1742558 A GB 1742558A GB 1742558 A GB1742558 A GB 1742558A GB 825475 A GB825475 A GB 825475A
Authority
GB
United Kingdom
Prior art keywords
alkylene oxide
alkanolamines
mixture
reaction
gas
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
GB1742558A
Inventor
Thomas Albert Joyce
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.)
Petrochemicals Ltd
Original Assignee
Petrochemicals 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 Petrochemicals Ltd filed Critical Petrochemicals Ltd
Priority to GB1742558A priority Critical patent/GB825475A/en
Publication of GB825475A publication Critical patent/GB825475A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C215/00Compounds containing amino and hydroxy groups bound to the same carbon skeleton
    • C07C215/02Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C215/04Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
    • C07C215/06Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
    • C07C215/12Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic the nitrogen atom of the amino group being further bound to hydrocarbon groups substituted by hydroxy groups

Landscapes

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

Abstract

Di- or tri-alkanolamines or a mixture comprising di- and tri-alkanolamines are prepared by passing a gas containing an alkylene oxide gaseous under the reaction conditions through a monoalkanolamine, dialkanolamine or a mixture of mono- and di-alkanolamines liquid under the reaction conditions and continuously venting from the reaction zone at least part of the gas. The gas mixture may contain an inert gas such as nitrogen. It is preferably passed through the alkanolamine starting material at a rate such that part of the alkylene oxide, preferably 1-5% by weight, remains unreacted. In a preferred embodiment the gas consists substantially of alkylene oxide free from inert gas. It is desirable to pass an inert gas, e.g. nitrogen, through the alkanolamine starting material to remove substances such as oxygen which would react with the alkylene oxide, and also through the product to remove unreacted alkylene oxide, or the latter may be removed by reducing the pressure. At atmospheric pressure, temperatures of 80-120 DEG C. are suggested for alkanolamines having less than 4 carbon atoms in each alkane radical. Pressures of 0.5 to 20 atmospheres are mentioned. Unreacted alkylene oxide vented from the reaction zone is normally absorbed, e.g. in alkanolamines, perhaps in aqueous solution or in acidified water. It is preferred that the carbon chains in the alkanolamine starting material contain 4 or less carbon atoms each and in the alkylene oxide 3 or less. The chains may be straight or branched. The progress of the reaction may be followed by the increase in volume of the liquid reaction mixture or by equivalent weight determinations. Examples describe the reaction of ethylene oxide with mono- and with di-ethanolamine to form triethanolamine and of propylene oxide with di-isopropanolamine to give a mixture of di- and tri-isopropanolamine which is then mixed with mono-isopropanolamine.
GB1742558A 1958-05-30 1958-05-30 Process for the production of alkanolamines Expired GB825475A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1742558A GB825475A (en) 1958-05-30 1958-05-30 Process for the production of alkanolamines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1742558A GB825475A (en) 1958-05-30 1958-05-30 Process for the production of alkanolamines

Publications (1)

Publication Number Publication Date
GB825475A true GB825475A (en) 1959-12-16

Family

ID=10094981

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1742558A Expired GB825475A (en) 1958-05-30 1958-05-30 Process for the production of alkanolamines

Country Status (1)

Country Link
GB (1) GB825475A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2307902A1 (en) * 1973-02-17 1974-10-03 Basf Ag PROCESS FOR THE PRODUCTION OF TRIAETHANOLAMINE
CN112851531A (en) * 2021-01-18 2021-05-28 南京红宝丽醇胺化学有限公司 Continuous preparation method of triisopropanolamine
CN114890905A (en) * 2022-05-20 2022-08-12 唐山冀东水泥外加剂有限责任公司 Method for synthesizing diethanolisopropanolamine

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2307902A1 (en) * 1973-02-17 1974-10-03 Basf Ag PROCESS FOR THE PRODUCTION OF TRIAETHANOLAMINE
CN112851531A (en) * 2021-01-18 2021-05-28 南京红宝丽醇胺化学有限公司 Continuous preparation method of triisopropanolamine
CN112851531B (en) * 2021-01-18 2022-04-19 南京红宝丽醇胺化学有限公司 Continuous preparation method of triisopropanolamine
CN114890905A (en) * 2022-05-20 2022-08-12 唐山冀东水泥外加剂有限责任公司 Method for synthesizing diethanolisopropanolamine

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