GB738184A - Improvements in or relating to process for the production of monoclinic glutamic acid crystals - Google Patents

Improvements in or relating to process for the production of monoclinic glutamic acid crystals

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Publication number
GB738184A
GB738184A GB3569/53A GB356953A GB738184A GB 738184 A GB738184 A GB 738184A GB 3569/53 A GB3569/53 A GB 3569/53A GB 356953 A GB356953 A GB 356953A GB 738184 A GB738184 A GB 738184A
Authority
GB
United Kingdom
Prior art keywords
glutamic acid
monoclinic
solution
crystals
acid hydrochloride
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
GB3569/53A
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.)
International Minerals and Chemical Corp
Original Assignee
International Minerals and Chemical Corp
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 International Minerals and Chemical Corp filed Critical International Minerals and Chemical Corp
Publication of GB738184A publication Critical patent/GB738184A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

An improvement or modification of the process for the production of monoclinic glutamic acid crystals of the parent Specification, is characterized by admixing with an aqueous solution containing between 4 per cent and 40 per cent glutamic acid hydrochloride with vigorous agitation sufficient sodium hydroxide or monosodium glutamate to adjust the pH of said mixture to between 2.5 and 4.0, said aqueous solution containing from the commencement of the pH adjustment up to about thirty seconds after the completion of said adjustment at least one monoclinic glutamic acid crystal nucleus, said adjustment being completed prior to the formation of any orthorhombic crystals, and recovering monoclinic glutamic acid crystals from the resultant crystal containing slurry. The monosodium glutamate and glutamic acid hydrochloride solutions employed may be prepared in any conventional manner from materials from which glutamic acid may be formed on hydrolysis such as animal and vegetable proteins and concentrated Steffen's filtrate and crude hydrolysate or prepared solutions may be employed in preparing the monoclinic glutamic acid. When seed crystals are employed they may be used in the form of a slurry or after separation from the mother liquor. In the original production of seed crystals sodium hydroxide or a solution containing monosodium glutamate is added to a solution containing between about 4 and about 20 per cent of glutamic acid hydrochloride. When solutions containing higher concentrations of glutamic acid hydrochloride are employed rapid stirring should be started as soon as crystallization of monoclinic crystals begins. The solutions may be mixed at atmospheric or higher temperatures. In a continuous process a slurry of monoclinic glutamic acid seed crystals in glutamic acid hydrochloride is prepared and rapidly agitated whilst glutamic acid hydrochloride solution and the solution which adjusts the pH of the mixture are added simultaneously and continuously. The mixture may take place in a small container and the slurry may be continuously removed to a larger container to crystallize the monoclinic glutamic acid. Batch processes may be operated. In examples: monoclinic glutamic acid is obtained when aqueous sodium hydroxide solution is added to aqueous glutamic acid hydrochloride solution to adjust the pH to between 3.0 and 3.3 within three to five seconds (1); aqueous monosodium glutamate solution is employed in a similar process instead of sodium hydroxide solution (2); monoclinic glutamic acid is obtained by adding concentrated sodium hydroxide solution to aqueous glutamic acid hydrochloride to which monoclinic glutamic acid seed crystals have been added. Specification 653,264 is referred to.
GB3569/53A 1952-03-03 1953-02-09 Improvements in or relating to process for the production of monoclinic glutamic acid crystals Expired GB738184A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US738184XA 1952-03-03 1952-03-03

Publications (1)

Publication Number Publication Date
GB738184A true GB738184A (en) 1955-10-12

Family

ID=22115978

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3569/53A Expired GB738184A (en) 1952-03-03 1953-02-09 Improvements in or relating to process for the production of monoclinic glutamic acid crystals

Country Status (1)

Country Link
GB (1) GB738184A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112521291A (en) * 2020-12-15 2021-03-19 梁山菱花生物科技有限公司 Glutamic acid crystal transformation method for shortening crystal transformation time

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112521291A (en) * 2020-12-15 2021-03-19 梁山菱花生物科技有限公司 Glutamic acid crystal transformation method for shortening crystal transformation time

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