GB911223A - Diethylyaminoethyl celluloses - Google Patents

Diethylyaminoethyl celluloses

Info

Publication number
GB911223A
GB911223A GB36277/59A GB3627759A GB911223A GB 911223 A GB911223 A GB 911223A GB 36277/59 A GB36277/59 A GB 36277/59A GB 3627759 A GB3627759 A GB 3627759A GB 911223 A GB911223 A GB 911223A
Authority
GB
United Kingdom
Prior art keywords
cellulose
mesh
water
amorphous
particles
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
GB36277/59A
Inventor
Arthur Ronald Lockwood
Alan Humphrey Raper
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.)
Glaxo Laboratories Ltd
Original Assignee
Glaxo Laboratories Ltd
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
Priority to NL257284D priority Critical patent/NL257284A/xx
Priority to NL127841D priority patent/NL127841C/xx
Application filed by Glaxo Laboratories Ltd filed Critical Glaxo Laboratories Ltd
Priority to GB36277/59A priority patent/GB911223A/en
Priority to DEG30747A priority patent/DE1215124B/en
Priority to CH1194260A priority patent/CH395956A/en
Priority to FR842106A priority patent/FR1271945A/en
Publication of GB911223A publication Critical patent/GB911223A/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14Hydrolases (3)
    • C12N9/24Hydrolases (3) acting on glycosyl compounds (3.2)
    • C12N9/2402Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
    • C12N9/2405Glucanases
    • C12N9/2408Glucanases acting on alpha -1,4-glucosidic bonds
    • C12N9/2411Amylases
    • C12N9/2414Alpha-amylase (3.2.1.1.)
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01DHARVESTING; MOWING
    • A01D87/00Loaders for hay or like field crops
    • A01D87/0038Dumpboxes or metering devices for loading or unloading
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J39/00Cation exchange; Use of material as cation exchangers; Treatment of material for improving the cation exchange properties
    • B01J39/08Use of material as cation exchangers; Treatment of material for improving the cation exchange properties
    • B01J39/16Organic material
    • B01J39/18Macromolecular compounds
    • B01J39/22Cellulose or wood; Derivatives thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J41/00Anion exchange; Use of material as anion exchangers; Treatment of material for improving the anion exchange properties
    • B01J41/08Use of material as anion exchangers; Treatment of material for improving the anion exchange properties
    • B01J41/12Macromolecular compounds
    • B01J41/16Cellulose or wood; Derivatives thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41NPRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
    • B41N3/00Preparing for use and conserving printing surfaces
    • B41N3/08Damping; Neutralising or similar differentiation treatments for lithographic printing formes; Gumming or finishing solutions, fountain solutions, correction or deletion fluids, or on-press development
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B11/00Preparation of cellulose ethers
    • C08B11/02Alkyl or cycloalkyl ethers
    • C08B11/04Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals
    • C08B11/14Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals with nitrogen-containing groups
    • C08B11/145Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals with nitrogen-containing groups with basic nitrogen, e.g. aminoalkyl ethers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D127/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
    • C09D127/02Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
    • C09D127/04Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C09D127/06Homopolymers or copolymers of vinyl chloride
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14Hydrolases (3)
    • C12N9/24Hydrolases (3) acting on glycosyl compounds (3.2)
    • C12N9/2402Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
    • C12N9/2405Glucanases
    • C12N9/2408Glucanases acting on alpha -1,4-glucosidic bonds
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14Hydrolases (3)
    • C12N9/24Hydrolases (3) acting on glycosyl compounds (3.2)
    • C12N9/2402Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
    • C12N9/2405Glucanases
    • C12N9/2408Glucanases acting on alpha -1,4-glucosidic bonds
    • C12N9/2411Amylases
    • C12N9/2414Alpha-amylase (3.2.1.1.)
    • C12N9/2417Alpha-amylase (3.2.1.1.) from microbiological source
    • C12N9/242Fungal source
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F11/00Chemical after-treatment of artificial filaments or the like during manufacture
    • D01F11/02Chemical after-treatment of artificial filaments or the like during manufacture of cellulose, cellulose derivatives, or proteins
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F2/00Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
    • D01F2/06Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from viscose

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Genetics & Genomics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Zoology (AREA)
  • Biomedical Technology (AREA)
  • Biotechnology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Medicinal Chemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Materials Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Textile Engineering (AREA)
  • Environmental Sciences (AREA)
  • Mycology (AREA)
  • Polymers & Plastics (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Abstract

An ion-exchange material comprises diethylaminoethyl cellulose, the cellulose having an essentially amorphous structure. It is made by reacting amorphous cellulose with an alkali metal hydroxide to form alkali cellulose, which is then reacted with a diethylhaloethylamine. Amorphous cellulose is made by very slow extrusion of viscose into an acid coagulating bath, no tension being applied to the filaments, which suitably are monofils of 1,000-60,000 denier and preferably of 25,000 denier. The monofils may be cut into pieces 1/4 inch in length, and milled to form particles not greater than 10 B.S. mesh, preferably between 16 and 52 B.S. mesh. The cellulose particles may then be treated with caustic soda, followed by diethylchloroethylamine. The material so made may be filled into a glass column as a suspension in water, buffered with 0,1 M sodium dihydrogen phosphate at pH 6,6, and used for purification or concentration of proteinceous material, e.g. a -amylase (see Group IV(b) or of poliomyelitis virus, Vitamin B12 acid (by adsorption) and Vitamin B12 (by adsorption of impurities while the vitamin passes through the column), or for the demineralisation of water.ALSO:Diethylaminoethyl cellulose, in which the cellulose residue has an essentially amorphous structure, is made by reacting amorphous cellulose with an alkali metal hydroxide to form alkali cellulose which is then reacted with a diethylhaloethylamine. Amorphous cellulose is made by very slow extrusion of viscose into an acid coagulating bath, no tension being applied to the filaments, which suitably are monofils of 1,000-60,000 denier and preferably of 25,000 denier. The monofils may be cut into pieces 1/4 inch in length, and milled to form particles not greater than 10 B.S. mesh, preferably between 16 and 52 B.S. mesh. The cellulose particles may then be treated with caustic soda, followed by diethylchloroethylamine. In an example, 1,058 Kg. of amorphous cellulose particles between 16 and 52 B.S. mesh are mixed at 11 DEG C. for one hour with 5,3:1 of 6N NaOH. A solution of 1,058 Kg. of diethylchloroethylamine hydrochloride in 1,6:1 of water is then added, and the whole mixed continuously for 35 minutes at 85 DEG C. The mixture is then cooled to room temperature and acidified with 2,5:1 concentrated hydrochloric acid, filtered, and the residue washed with 12:1 tap water, 5,3:1 N.NaOH and then with tap water until the washings are almost neutral. For the application of the product as an ion-exchange material, (see Group III).ALSO:a -Amylase may be separated, purified and concentrated by means of an ion-exchange material comprising diethylaminoethyl cellulose the cellulose having an essentially amorphous structure. The ion-exchange material is made by reacting amorphous cellulose with an alkali metal hydroxide to form alkali cellulose, which is then reacted with a diethylhaloethylamine. Amorphous cellulose is made by very slow extrusion of viscose into an acid coagulating bath, no tension being applied to the filaments, which suitably are monofils of 1,000-60,000 denier and preferably of 25,000 denier. The monofils may be cut into pieces 1/4 inch in length, and milled to form particles not greater than 10 B.S. mesh, preferably between 16 and 52 B.S. mesh. The cellulose particles may then be treated with caustic soda, followed by diethylchloroethylamine. In an example, 1.058 Kg. of amorphous cellulose particles between 16 and 52 B.S. mesh are mixed at 11 DEG C. for one hour with 5.3 l. of 6N NaOH. A solution of 1.058 Kg. of diethylchloroethylamine hydrochloride in 1.6 l. of water is then added, and the whole mixed continuously for 35 minutes at 85 DEG C. The mixture is then cooled to room temperature and acidified with 2.5 l. concentrated hydrochloric acid, filtered, and the residue washed with 12 l. tap water, 5.3 l. N.NaOH and then with tap water until the washings are almost neutral. The material so made may be filled into a 10 ft. X 2 in. glass column as a suspension in water to give a 7 ft. bed of about 4.2 l. volume. The bed is then buffered with 8.4 l. 0.1 M sodium dihydrogen phosphate at pH 6.6 fed downflow at 8.4 l./hr. In an example, 75 l. of fungal a -amylase broth at a dextrinising activity of 14.0 units/ml., equivalent to 1,050 kilo units total activity, are adjusted to pH 6.6 with acetic acid, passed through a sterilising grade of filter paper and fed downflow through the bed at 4.2 l./hr. followed by 4.2 l. water as displacement wash at 4.2 l./hr. Analysis of the column effluent showed 1.7 kilo units total dextrinising activity, giving 1,048.3 kilo units adsorbed, equivalent to 99.8% efficiency. The adsorbed amylase is recovered by downflow elution with 4.2 l. 0.8 M sodium acetate/0.8 M sodium chloride buffer at pH 4.7 followed by a 4.2 l. displacement water wash, all at 2.1 l./hr. A 7 l. portion of the eluate contained 992.2 kilo units total dextrinising activity, representing 94.6% efficiency and a ten fold concentration of the original broth.ALSO:Poliomyelitis virus may be purified or concentrated by means of an ion-exchange material comprising diethylaminoethyl cellulose, the cellulose having an essentially amorphous structure. The ion-exchange material is made by reacting amorphous cellulose with an alkali metal hydroxide to form alkali cellulose, which is then reacted with a diethylhaloethyl amine. The material so made may be filled into a 10 feet x 2 inches glass column as a suspension in water to give a 7 feet bed of about 4.2 1. volume. The bed is then buffered with 8.4 1. 0.1 M sodium dihydrogen phosphate at pH 6.6 fed downflow at 8.4 1/hr.
GB36277/59A 1959-10-26 1959-10-26 Diethylyaminoethyl celluloses Expired GB911223A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
NL257284D NL257284A (en) 1959-10-26
NL127841D NL127841C (en) 1959-10-26
GB36277/59A GB911223A (en) 1959-10-26 1959-10-26 Diethylyaminoethyl celluloses
DEG30747A DE1215124B (en) 1959-10-26 1960-10-21 Process for the production of diaethylaminoethyl cellulose ethers which can be used as anion exchangers
CH1194260A CH395956A (en) 1959-10-26 1960-10-25 Process for the production of an ion exchanger
FR842106A FR1271945A (en) 1959-10-26 1960-10-25 New cellulose derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB36277/59A GB911223A (en) 1959-10-26 1959-10-26 Diethylyaminoethyl celluloses

Publications (1)

Publication Number Publication Date
GB911223A true GB911223A (en) 1962-11-21

Family

ID=10386639

Family Applications (1)

Application Number Title Priority Date Filing Date
GB36277/59A Expired GB911223A (en) 1959-10-26 1959-10-26 Diethylyaminoethyl celluloses

Country Status (5)

Country Link
CH (1) CH395956A (en)
DE (1) DE1215124B (en)
FR (1) FR1271945A (en)
GB (1) GB911223A (en)
NL (2) NL127841C (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2073697A5 (en) * 1969-12-22 1971-10-01 Baxter Laboratories Inc
US3785771A (en) * 1969-08-19 1974-01-15 Du Pont Method and apparatus for analyzing a liquid containing macromolecules that would interfere with the analysis
EP0185379A2 (en) * 1984-12-20 1986-06-25 NABISCO BRANDS, Inc. A process for the production of purified glucose isomerase

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2422699A1 (en) * 1978-04-12 1979-11-09 Merieux Inst Materials for affinity chromatography of biological macromolecules - comprise support coated with polysaccharide coupled to amine

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3785771A (en) * 1969-08-19 1974-01-15 Du Pont Method and apparatus for analyzing a liquid containing macromolecules that would interfere with the analysis
FR2073697A5 (en) * 1969-12-22 1971-10-01 Baxter Laboratories Inc
EP0185379A2 (en) * 1984-12-20 1986-06-25 NABISCO BRANDS, Inc. A process for the production of purified glucose isomerase
EP0185379A3 (en) * 1984-12-20 1988-05-11 NABISCO BRANDS, Inc. A process for the production of purified glucose isomerase

Also Published As

Publication number Publication date
DE1215124B (en) 1966-04-28
FR1271945A (en) 1961-09-15
CH1194260A4 (en) 1966-01-14
NL257284A (en)
CH395956A (en) 1966-01-14
NL127841C (en)

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