GB799752A - Citric acid production - Google Patents

Citric acid production

Info

Publication number
GB799752A
GB799752A GB2079/55A GB207955A GB799752A GB 799752 A GB799752 A GB 799752A GB 2079/55 A GB2079/55 A GB 2079/55A GB 207955 A GB207955 A GB 207955A GB 799752 A GB799752 A GB 799752A
Authority
GB
United Kingdom
Prior art keywords
citric acid
medium
fermentation
carbohydrate
per cent
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
GB2079/55A
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.)
Bayer Corp
Original Assignee
Miles Laboratories Inc
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 Miles Laboratories Inc filed Critical Miles Laboratories Inc
Publication of GB799752A publication Critical patent/GB799752A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00Preparation of oxygen-containing organic compounds
    • C12P7/40Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
    • C12P7/44Polycarboxylic acids
    • C12P7/48Tricarboxylic acids, e.g. citric acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42Separation; Purification; Stabilisation; Use of additives
    • C07C51/43Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Microbiology (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Biotechnology (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Citric acid is obtained from an impure carbohydrate-containing material by deionizing an aqueous solution of the carbohydrate-containing material to reduce the ion concentration thereof to the equivalent of from 5 to 10 parts per million of sodium chloride as measured by conductivity methods, acidifying the de-ionized solution to pH 2.2 to 2.8, fermenting the solution with citric acid producing fungi under submerged fermentation conditions, removing the fungi by filtration to yield a citric acid containing liquor, heating the liquor to concentrate the citric acid therein by evaporative removal of water, and cooling the concentrated liquor to crystallize solid citric acid. The fermentation medium may be derived from invert molasses, corn starch hydrolysate or beet molasses and is suitably an aqueous solution of carbohydrate material in an amount approximating to about 10 to 15 per cent of sucrose, dextrose, levulose or glucose. The impure carbohydrate solution may be submitted to a preliminary treatment for removal of impurities by the addition of lime or an insoluble hydroxide of a heavy metal and the deionization may be effected by subjecting the impure solution to the action of a cation exchange resin, e.g. one operating on the hydrogen cycle, and this treatment should be continued until the Fe concentration is below 4 parts per million whilst other cations such as those of lead, mercury, copper and cobalt are simultaneously removed. In those cases where the total concentration of ions is high treatment with an anion exchange resin is also necessary in order to remove interfering quantities of anions but with purer carbohydrate sources a simple removal of cations by the use of a cation exchange resin may be sufficient. To such a purified carbohydrate medium various nutrient salts are added in the following amounts: 0.15 to 0.2 per cent of ammonium carbonate, 0.01 to 0.02 per cent of potassium acid phosphate, 0.08 to 0.15 per cent of hydrated magnesium sulphate and 0.0002 to 0.0004 per cent of zinc in the form of zinc chloride or other soluble zinc salt. This medium is then brought to a pH of 2.2 to 2.8 by the addition of hydrochloric acid and is then introduced into a fermenter the contents of which are sterilized by bringing the temperature of the medium to 180 DEG F. for two hours. After allowing the medium to cool to about room temperature any fungi capable of producing citric acid are added in concentrations of about 5 million to about 25 million spores per litre of fermentation medium, a vast preponderance of the spores being disposed beneath the surface of the medium. Best results are obtained by using selected mutants and wild strains of Aspergillus niger. Sterile air is then introduced into the inoculated medium, between one tenth volume and one volume of air per volume of medium per minute being generally employed. Anti-foam agent is added as necessary and the temperature is maintained at 24 DEG to 34 DEG C. during the fermentation, 8 to 12 days being generally required to complete the fermentation. On completion of the fermentation the contents are withdrawn and the mycelium which has grown from the spores is removed by filtration which optimumly will include a clarifying filtration using a commercially available activated carbon. The filtered liquor which normally contains about 10 to 12 per cent of citric acid is then concentrated by evaporation at elevated temperature and preferably under reduced pressure, until its volume is reduced to about one tenth to one fourteenth of its volume after fermentation and on cooling and stirring the citric acid will crystallize and can be removed by centrifugation or filtration. The recovered crystals may be further purified by recrystallization by cooling a hot saturated aqueous solution thereof. Examples are given for the crystallization of citric acid from fermented liquors prepared from a corn sugar solution and from a beet molasses fermentation liquor, the carbohydrate medium being first deionized and acidified to a pH of 2.2 to 2.8 as above.
GB2079/55A 1954-02-12 1955-01-24 Citric acid production Expired GB799752A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US799752XA 1954-02-12 1954-02-12

Publications (1)

Publication Number Publication Date
GB799752A true GB799752A (en) 1958-08-13

Family

ID=22153995

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2079/55A Expired GB799752A (en) 1954-02-12 1955-01-24 Citric acid production

Country Status (3)

Country Link
DE (1) DE1018374B (en)
FR (1) FR1118674A (en)
GB (1) GB799752A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105797422A (en) * 2016-04-20 2016-07-27 西安航天华威化工生物工程有限公司 Citric acid continuous cooling crystallization system and method thereof
CN109970546A (en) * 2017-12-28 2019-07-05 华东理工大学 A kind of preparation method and its device of electronic grade citric acid
CN111675610A (en) * 2020-06-18 2020-09-18 湖南新绿方药业有限公司 Refining method for preparing high-purity non-caking fine-particle citric acid crystal

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US515033A (en) * 1894-02-20 Carl wehmer
DE551930C (en) * 1925-12-09 1932-06-08 Auguste Fernbach Process for the production of citric acid using mushrooms
DE619977C (en) * 1930-10-04 1935-10-10 Wilhelm Klapproth Dr Ing Process for the production of citric acid by fermentation
NL76900C (en) * 1935-04-04
US2492673A (en) * 1947-04-21 1949-12-27 Miles Lab Conditioning molasses and the like for production of citric acid by fermentation

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105797422A (en) * 2016-04-20 2016-07-27 西安航天华威化工生物工程有限公司 Citric acid continuous cooling crystallization system and method thereof
CN109970546A (en) * 2017-12-28 2019-07-05 华东理工大学 A kind of preparation method and its device of electronic grade citric acid
CN111675610A (en) * 2020-06-18 2020-09-18 湖南新绿方药业有限公司 Refining method for preparing high-purity non-caking fine-particle citric acid crystal
CN111675610B (en) * 2020-06-18 2023-08-29 湖南新绿方药业有限公司 Refining method for preparing high-purity non-caking fine-particle citric acid crystals

Also Published As

Publication number Publication date
FR1118674A (en) 1956-06-08
DE1018374B (en) 1957-10-31

Similar Documents

Publication Publication Date Title
Currie The citric acid fermentation of Aspergillus niger
AU2011214268B2 (en) Process for manufacturing succinic acid
BRPI0703692B1 (en) A method for obtaining the crystals of a basic amino acid hydrochloride comprising generating a basic amino acid using microbial cells by fermentation in a fermentation broth or by an enzymatic method in an enzyme reaction solution using the cells as catalysts.
US4828993A (en) Process for the preparation of organic acids
HU214675B (en) Method for separing lysine from aqueous solution
DE3063910D1 (en) Production of fructose and useful by-products
US2024565A (en) Process for the production of lactic acid
GB907321A (en) Improvements in the manufacture of lactic acid
GB799752A (en) Citric acid production
US20070037266A1 (en) Process for producing erythritol
US3689362A (en) Enzymatic method for manufacture of fructose
US2326986A (en) Process for the production of fumaric acid
US3050444A (en) Method for the production of levulose
GB2085884A (en) Crystals of beta -nicotinamide- adenine-dinucleotide and process for preparing the same
US2729587A (en) Production of fructose
US3044941A (en) Process for producing itaconic acid
US3576718A (en) Process of producing gluconic acid and gluconates
DE60020483T2 (en) Process for the production of citric acid
JPS6338B2 (en)
US2142739A (en) Fermentation process of treating sulphite waste liquor
US2883329A (en) Process for producing citric acid
EP0737753A2 (en) Process for the production of sugar from raw juice of sugar beet
US5041645A (en) Method for the preparation and recovery of alkali metal citrates
US2686777A (en) Isolation of dextran by alkaline earth hydroxide complex formation and products thereof
JPS5886091A (en) Preparation of citric acid