GB130968A - Improvements in Continuous Process for the Manufacture of Esters. - Google Patents
Improvements in Continuous Process for the Manufacture of Esters.Info
- Publication number
- GB130968A GB130968A GB15775/19A GB1577519A GB130968A GB 130968 A GB130968 A GB 130968A GB 15775/19 A GB15775/19 A GB 15775/19A GB 1577519 A GB1577519 A GB 1577519A GB 130968 A GB130968 A GB 130968A
- Authority
- GB
- United Kingdom
- Prior art keywords
- still
- pipe
- alcohol
- methyl
- methyl acetate
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/12—Acetic acid esters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
- B01D3/34—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping with one or more auxiliary substances
- B01D3/36—Azeotropic distillation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/08—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/22—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
130,968. U.S. Industrial Alcohol Co., (Assignees of Backhaus, A. A.). Aug. 7, 1918, [Convention date]. Distilling-plant.-Esters are prepared in a continuous manner by feeding an alcohol, an organic acid, and a catalyst, either separately or mixed together, to a column still while distilling off the ester formed. The production of methyl acetate from methyl alcohol, dilute or glacial acetic acid, and sulphuric acid is described. Using the apparatus shown in Fig. 1, sulphuric acid, dilute acetic acid, and methyl alcohol are fed continuously in regulated amounts from tanks 8, 12, 18 respectively by pipes 7, 11, 15 to a column still 1 of ordinary construction; at the commencement sufficient methyl alcohol is run in to seal all the plates in the still. Vapours of methyl acetate and alcohol pass off by pipe 22 to a dephlegmator 23; condensed alcohol runs back from the dephlegmator to the still by pipe 24, while methyl acetate vapours pass off by pipe 25 to a second column still 26. From this still the methyl acetate vapours pass by pipe 27<1> to a dephlegmator 28, condensed alcohol flows back by pipe 29 to the top of still 26, while the methyl acetate vapours pass on to a condenser 31. A pipe 27 leads methyl alcohol from the lower part of still 26 to the still 1. Water and sulphuric acid flow from the bottom of still 1 by a pipe 20. The apparatus shown in Fig. 2 is similar in all respects except the feed device. Sulphuric acid, acetic acid (in this case glacial), and methyl alcohol are fed from tanks 42, 46, 50 respectively to a mixing-tank 35 which contains a rotary stirrer 36, and after undergoing partial reaction in the mixing-tank, the mixture is fed to the still by pipe 34; an initial charge of methyl alcohol as before is fed to the still by pipe 50<a>. Specifications 130,969 and 130,970 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US248754A US1400849A (en) | 1918-08-07 | 1918-08-07 | Continuous process for the manufacture of esters |
Publications (1)
Publication Number | Publication Date |
---|---|
GB130968A true GB130968A (en) | 1920-08-12 |
Family
ID=22940529
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB15776/19A Expired GB130969A (en) | 1918-08-07 | 1919-06-23 | Improvements in Apparatus for the Manufacture of Esters. |
GB15775/19A Expired GB130968A (en) | 1918-08-07 | 1919-06-23 | Improvements in Continuous Process for the Manufacture of Esters. |
GB15777/19A Expired GB130970A (en) | 1918-08-07 | 1919-06-23 | Improvements in Apparatus for the Production of Esters. |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB15776/19A Expired GB130969A (en) | 1918-08-07 | 1919-06-23 | Improvements in Apparatus for the Manufacture of Esters. |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB15777/19A Expired GB130970A (en) | 1918-08-07 | 1919-06-23 | Improvements in Apparatus for the Production of Esters. |
Country Status (3)
Country | Link |
---|---|
US (1) | US1400849A (en) |
FR (3) | FR501499A (en) |
GB (3) | GB130969A (en) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL72344C (en) * | 1947-11-03 | 1952-12-15 | ||
US2645660A (en) * | 1951-05-16 | 1953-07-14 | Standard Oil Dev Co | Excess acid process for the manufacture of esters |
ZA816748B (en) * | 1980-10-01 | 1982-10-27 | Hoechst Ag | Process for the preparation of an ethyl ester |
US4435595A (en) * | 1982-04-26 | 1984-03-06 | Eastman Kodak Company | Reactive distillation process for the production of methyl acetate |
GB0325530D0 (en) * | 2003-10-31 | 2003-12-03 | Davy Process Techn Ltd | Process |
CN1902144B (en) * | 2003-12-12 | 2010-06-09 | 滑铁卢大学 | Composite catalyst for the selective oligomerization of lower alkenes and the production of high octane products |
US7667068B2 (en) * | 2004-07-19 | 2010-02-23 | Board Of Trustees Of Michigan State University | Process for reactive esterification distillation |
US7652167B2 (en) * | 2004-07-19 | 2010-01-26 | Board Of Trustees Of Michigan State University | Process for production of organic acid esters |
DE102004056672A1 (en) * | 2004-11-24 | 2006-06-01 | Basf Ag | Process for the chemical reaction and separation of a mixture in a column |
FR2957918B1 (en) | 2010-03-25 | 2012-07-13 | Rhodia Poliamida E Especialidades Ltda | PROCESS FOR OBTAINING A CARBOXYLIC ACID ESTER |
EP4076532A4 (en) * | 2019-12-16 | 2023-09-13 | Eastman Chemical Company | Esterification of acetic acid recovered from wood acetylation with alcohols |
CN111747828B (en) * | 2020-07-23 | 2023-05-26 | 浙江皇马科技股份有限公司 | Preparation method and system of ethylene glycol monopropyl ether |
-
1918
- 1918-08-07 US US248754A patent/US1400849A/en not_active Expired - Lifetime
-
1919
- 1919-06-23 GB GB15776/19A patent/GB130969A/en not_active Expired
- 1919-06-23 GB GB15775/19A patent/GB130968A/en not_active Expired
- 1919-06-23 GB GB15777/19A patent/GB130970A/en not_active Expired
- 1919-07-08 FR FR501499A patent/FR501499A/en not_active Expired
- 1919-07-08 FR FR501500A patent/FR501500A/en not_active Expired
- 1919-07-08 FR FR501501A patent/FR501501A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR501501A (en) | 1920-04-16 |
FR501500A (en) | 1920-04-15 |
GB130970A (en) | 1920-09-23 |
US1400849A (en) | 1921-12-20 |
GB130969A (en) | 1920-09-23 |
FR501499A (en) | 1920-04-15 |
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