GB804970A - Improvements in or relating to the purification of lysine - Google Patents

Improvements in or relating to the purification of lysine

Info

Publication number
GB804970A
GB804970A GB23621/57A GB2362157A GB804970A GB 804970 A GB804970 A GB 804970A GB 23621/57 A GB23621/57 A GB 23621/57A GB 2362157 A GB2362157 A GB 2362157A GB 804970 A GB804970 A GB 804970A
Authority
GB
United Kingdom
Prior art keywords
lysine
resin
sulphonated
per cent
resins
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
GB23621/57A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB804970A publication Critical patent/GB804970A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/38Separation; Purification; Stabilisation; Use of additives
    • C07C227/40Separation; Purification

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

An impure aqueous solution of lysine or a water-soluble salt thereof containing amine impurities including one or both of di- and tri-(5-amino-5-carboxypentyl) amine is purified by passage through a strongly oxidic cationexchange resin, removing at least part of said amine impurities from the resin and subsequently removing lysine of increased purity from the resin. The purification may be effected in two preferred ways. Using low lysine loading of the resin, the solution is passed through a bed of resin in the acid or ammonium form, preferably the former, to absorb lysine and impurities, and the latter selectively eluted with dilute aqueous ammonia, preferably of concentration 0.1-0.7 per cent NH3, through an unloaded portion of the bed in the ammonium form, such unloaded portion preferably being at least one-third the length, more preferably one to two times the length of the loaded portion; the lysine remaining on the resin is subsequently eluted. Using high lysine loading of the resin, the solution is passed through a bed of the resin in the ammonium form until the bed is substantially completely loaded with lysine and preferably overloaded, preferably until 0.1-15 per cent, more preferably 2-10 per cent, of the lysine fed to the column has passed into the effluent. After a water wash, the lysine is eluted from the resin. The elution of lysine is preferably effected with aqueous ammonia of strength 5-29 per cent NH3. Preferably room temperature is used. Suitable resins are those having strongly acidic functional groups such as sulphonic, phosphonic or phosphorous acid groups. Preferred resins are the sulphonic acid type such as sulphonated coals, sulphonated phenol-aldehyde resins and nuclear sulphonated aromatic hydrocarbon resins. Particularly preferred are the nuclear sulphonated aromatic hydrocarbon cross-linked resins such as the sulphonated copolymers of a monovinylbenzene and a polyvinylbenzene, particularly sulphonated styrene-divinylbenzene copolymers having the equivalent of from 4-16 per cent divinylbenzene. The resin is used in particulate form, generally of 20-100 mesh, and preferably of 20-50 mesh (U.S. Standard screen scale). Repeated purification and re-cycling may be employed. Examples describe various procedures of the process of the invention.
GB23621/57A 1956-08-01 1957-07-25 Improvements in or relating to the purification of lysine Expired GB804970A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US804970XA 1956-08-01 1956-08-01

Publications (1)

Publication Number Publication Date
GB804970A true GB804970A (en) 1958-11-26

Family

ID=22157762

Family Applications (1)

Application Number Title Priority Date Filing Date
GB23621/57A Expired GB804970A (en) 1956-08-01 1957-07-25 Improvements in or relating to the purification of lysine

Country Status (1)

Country Link
GB (1) GB804970A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4835309A (en) * 1988-04-14 1989-05-30 Eastman Kodak Company Ion exchange recovery of L-lysine

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4835309A (en) * 1988-04-14 1989-05-30 Eastman Kodak Company Ion exchange recovery of L-lysine

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