GB766685A - Improvements in or relating to process for the recovery of glutamic acid - Google Patents
Improvements in or relating to process for the recovery of glutamic acidInfo
- Publication number
- GB766685A GB766685A GB16305/54A GB1630554A GB766685A GB 766685 A GB766685 A GB 766685A GB 16305/54 A GB16305/54 A GB 16305/54A GB 1630554 A GB1630554 A GB 1630554A GB 766685 A GB766685 A GB 766685A
- Authority
- GB
- United Kingdom
- Prior art keywords
- glutamic acid
- crystallizing
- sulphuric acid
- filtrate
- acid
- 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
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/38—Separation; Purification; Stabilisation; Use of additives
- C07C227/40—Separation; Purification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Peptides Or Proteins (AREA)
Abstract
Glutamic acid is obtained by hydrolysing precursors thereof, neutralizing the hydrolysate with an agent which forms an insoluble salt with the hydrolytic agent, separating off the salt, adjusting the pH of the filtrate to 2.5-4.0 with sulphuric acid, crystallizing out glutamic acid, adjusting the pH of the mother liquor to 1.0-3.5 with sulphuric acid, adding sufficient methanol to precipitate ash-forming material and crystallizing glutamic acid from the filtrate at its isoelectric point. The latter step is facilitated by passing the solution through a cation or anion exchanger, subsequently eluting the adsorbed glutamic acid and crystallizing it at pH 2.5-4.0. The process is applicable to the treatment of desugarized beet molasses or proteinaceous materials such as gluten. Hydrolysis may be effected with barium or calcium hydroxide and the metal subsequently precipitated at pH 6-10, preferably 7-10, with carbon dioxide, sulphur dioxide (or salts thereof) or sulphuric acid. It is advantageous to bring the pH first to 4.5-5.5 and concentrate and filter the solution before the final adjustment of the pH. An example is given of the process. Specifications 655,841, 742,497 and U.S.A. Specification 2,586,295 are referred to. Reference has been directed by the Comptroller to Specification 644,382.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US766685XA | 1953-07-01 | 1953-07-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB766685A true GB766685A (en) | 1957-01-23 |
Family
ID=22133480
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16305/54A Expired GB766685A (en) | 1953-07-01 | 1954-06-02 | Improvements in or relating to process for the recovery of glutamic acid |
Country Status (4)
Country | Link |
---|---|
BE (1) | BE530054A (en) |
DE (1) | DE1005521B (en) |
FR (1) | FR1167460A (en) |
GB (1) | GB766685A (en) |
-
0
- BE BE530054D patent/BE530054A/xx unknown
-
1954
- 1954-06-02 GB GB16305/54A patent/GB766685A/en not_active Expired
- 1954-06-28 DE DEI8842A patent/DE1005521B/en active Pending
- 1954-06-29 FR FR1167460D patent/FR1167460A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
BE530054A (en) | |
DE1005521B (en) | 1957-04-04 |
FR1167460A (en) | 1958-11-25 |
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