GB422139A - Improvements in the manufacture and production of trimethylamine - Google Patents

Improvements in the manufacture and production of trimethylamine

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Publication number
GB422139A
GB422139A GB1940433A GB1940433A GB422139A GB 422139 A GB422139 A GB 422139A GB 1940433 A GB1940433 A GB 1940433A GB 1940433 A GB1940433 A GB 1940433A GB 422139 A GB422139 A GB 422139A
Authority
GB
United Kingdom
Prior art keywords
ammonia
substance
trimethylamine
azeotropic mixture
distillation
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
GB1940433A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB1940433A priority Critical patent/GB422139A/en
Publication of GB422139A publication Critical patent/GB422139A/en
Expired legal-status Critical Current

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Abstract

Trimethylamine is separated from mixtures thereof with ammonia by distillation in the presence of a third substance which forms with ammonia an azeotropic mixture of lower boiling point than the azeotropic mixture of trimethylamine and ammonia, but does not form a ternary azeotropic mixture with trimethylamine and ammonia. Suitable substances are low-boiling aliphatic hydrocarbons and ethers. The distillation is preferably effected at a raised pressure, e.g. at the vapour pressure of the mixture at atmospheric temperature, but distillation may also be effected at atmospheric or reduced pressure. When the boiling point of the third substance differs considerably from that of trimethylamine, an excess of the third substance may be added, so that all the ammonia may be removed as azeotropic mixture and the excess of third substance then distilled off. When the boiling point of the third substance is close to that of trimethylamine, the amount of substance added is preferably rather less than is necessary to remove all the ammonia as azeotropic mixture, the remainder of the ammonia being removed as ammonia-trimethylamine mixture. Examples are given describing the distillation of ammoniatrimethylamine mixtures in the presence of n-butane, isobutane, and dimethyl ether; the use of n- or iso-butylene as the third substance is also mentioned. When dimethyl ether is used, the azeotropic mixture can be used, with or without addition of ammonia and methyl alcohol, for the catalytic manufacture of methylamines.ALSO:Trimethylamine is separated from mixtures thereof with ammonia by distillation in the presence of a third substance which forms with ammonia an azeotropic mixture of lower boiling point than the azeotropic mixture of trimethylamine and ammonia, but does not form a ternary azeotropic mixture with trimethylamine and ammonia. Suitable substances are low-boiling aliphatic hydrocarbons and ethers. The distillation is preferably effected at a raised pressure, e.g. at the vapour pressure of the mixture at atmospheric temperature, but distillation may also be effected at atmospheric or reduced pressure. When the boiling point of the third substance differs considerably from that of trimethylamine, an excess of the third substance may be added, so that all the ammonia may be removed as azeotropic mixture and the excess of third substance then distilled off. When the boiling point of the third substance is close to that of trimethylamine, the amount of substance added is preferably rather less than is necessary to remove all the ammonia as azeotropic mixture, the remainder of the ammonia being removed as ammoniatrimethylamine mixture. Examples are given describing the distillation of ammonia-trimethylamine mixtures in the presence of n-butane, isobutane, and dimethyl ether; the use of n-or iso-butylene as the third substance is also mentioned.
GB1940433A 1933-07-08 1933-07-08 Improvements in the manufacture and production of trimethylamine Expired GB422139A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1940433A GB422139A (en) 1933-07-08 1933-07-08 Improvements in the manufacture and production of trimethylamine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1940433A GB422139A (en) 1933-07-08 1933-07-08 Improvements in the manufacture and production of trimethylamine

Publications (1)

Publication Number Publication Date
GB422139A true GB422139A (en) 1935-01-07

Family

ID=10128783

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1940433A Expired GB422139A (en) 1933-07-08 1933-07-08 Improvements in the manufacture and production of trimethylamine

Country Status (1)

Country Link
GB (1) GB422139A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2444175A (en) * 1944-10-12 1948-06-29 Sinclair Refining Co Separation of ammonia and hydrocarbons from mixtures containing ammonia, propane, propylene, and higher boiling materials
US2461010A (en) * 1942-12-29 1949-02-08 Sinclair Refining Co Process for the recovery of ammonia

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2461010A (en) * 1942-12-29 1949-02-08 Sinclair Refining Co Process for the recovery of ammonia
US2444175A (en) * 1944-10-12 1948-06-29 Sinclair Refining Co Separation of ammonia and hydrocarbons from mixtures containing ammonia, propane, propylene, and higher boiling materials

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