Claims
- 1. A process for the preparation of porous cellulose beads suitable for use as a carrier of enzymes and other biological agents which comprises the steps of:
- a. dissolving a hydrolyzable cellulose derivative in an inert organic, water-miscible solvent to form a solution having a density greater than that of a precipitation solution the cellulose derivative to solvent ratio ranging from 1:20 to 1:3 weight/volume;
- b. distributing said solution in the form of droplets into a precipitation solution whereby said cellulose derivative is precipitated in the form of uniformly porous beads;
- c. separating the precipitated beads from said solution;
- d. washing the separated porous beads with water;
- e. hydrolyzing the washed beads to convert the beads to cellulose and to increase the active sites for attachment of enzymes and other biological agents;
- f. washing the hydrolyzed beads to obtain porous cellulose beads having a uniformly distributed void space greater than 50% by volume.
- 2. A process according to claim 1 wherein distributing is accomplished by spraying.
- 3. A process according to claim 1 wherein said precipitation solution is selected from the group consisting of water, hexane, cyclohexane, octane, benzene and mixtures of water and ethanol or methanol.
- 4. A process according to claim 3 wherein said precipitation solution is water.
- 5. A process according to claim 1 wherein said cellulose derivative is cellulose acetate and hydrolysis is carried out in a caustic solution.
- 6. A process according to claim 1 wherein said solvent is a mixture of:
- a. a member from the group consisting of acetone, a mixture of acetone and methanol or ethanol, methyl acetate, a mixture of methylene dichloride and methanol, methyl ethyl ketone, formamide and dimethyl sulfoxide; and
- b. a member from the group consisting of dimethyl sulfoxide, formamide, methyl acetate, cyclohexanone, methylene dichloride, ethylene dichloride, a mixture of methylene dichloride and methanol, and a mixture of ethylene dichloride and methanol.
- 7. A process according to claim 6 wherein said solvent is dimethyl sulfoxide, formamide or methyl acetate.
- 8. A process according to claim 1 wherein the void space of said beads is from about 75 to 95%.
- 9. A process according to claim 1 wherein said porous cellulose beads are cross-linked with at least one cross-linking agent to obtain cross-linked porous cellulose beads.
- 10. A process according to claim 9 wherein said beads are cross-linked prior to being hydrolyzed.
- 11. A process according to claim 9 wherein said beads are cross-linked after being hydrolyzed.
- 12. A process according to claim 9 wherein said cross-linking agent is a diisocyanate.
- 13. A process according to claim 12 wherein said diisocyanate is tolylene-2,4-diisocyanate or hexamethylene diisocyanate.
- 14. A process according to claim 9 wherein said cross-linking agent is epichlorohydrin in a sodium hydroxide solution.
- 15. A process according to claim 9 wherein said cross-linking agent is formaldehyde in a hydrochloric acid solution.
- 16. A process according to claim 9 wherein said cross-linking agent is glutaraldehyde.
- 17. Porous cellulose beads produced according to the process of claim 1.
- 18. Porous cross-linked cellulose beads produced according to the method of claim 9.
- 19. A method for the removal of metallic ions from a dilute solution containing said ions which comprises contacting the dilute solution with the porous cellulose beads of claim 17, said beads being further characterized by the presence of functional groups capable of attaching said ions to the beads.
- 20. A method for the separation and purification of enzymes, proteins, and nucleic acids which comprises contacting enzymes, proteins or nucleic acids with the porous beads of claim 17, said beads being further characterized by the presence of functional groups capable of attaching said enzymes, proteins or nucleic acids.
Parent Case Info
This application is a continuation-in-part of our co-pending application Ser. No. 679,497 filed Apr. 22, 1976.
US Referenced Citations (14)
Non-Patent Literature Citations (1)
Entry |
Tsumura et al., "Continuous Isomerization of Glucose by a Column of Glucose Isomerase," Journal of Food Science and Technology, vol. 14, No. 12, pp. 539-540 (1967). |
Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
679497 |
Apr 1976 |
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