Method for producing psicose

US12024751B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12024751-B2
Application numberUS-201716464356-A
CountryUS
Kind codeB2
Filing dateNov 24, 2017
Priority dateDec 8, 2016
Publication dateJul 2, 2024
Grant dateJul 2, 2024

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The present invention relates to a method for effectively utilizing fructose raffinate obtained in the process for separating psicose conversion product with a high purity chromatography in the process for preparing psicose, and more specifically, it is utilized for preparation of fructose-containing raw material solution for preparing psicose by supplying the fructose raffinate obtained in the separation step of psicose preparation into the psicose conversion reaction.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method of preparation for psicose comprising: separating psicose conversion product of a psicose conversion reaction with a simulated moving bed (SMB) chromatography separation process to obtain a psicose fraction and a fructose raffinate, and recycling the fructose raffinate as a first fructose raw material into the psicose conversion reaction, mixing the fructose raffinate with a fresh fructose raw material as a second fructose raw material, before being recycled to the psicose conversion reaction, wherein a mixing ratio of the fructose raffinate and the second fructose raw material (raffinate:second fructose raw material) is a volume ratio of 1:0.9 to 1.5, when the fructose raffinate and the second fructose raw material have 50 Brix. 2. The method of preparation of claim 1 , wherein the psicose conversion product is obtained by a biological psicose conversion process using fructose-containing raw material. 3. The method of preparation of claim 1 , wherein a mixing ratio of the fructose raffinate and the second fructose raw material (raffinate:second fructose raw material) is a volume ratio of 1:0.95 to 1.15 or 1:1.05 to 1.2, when the fructose raffinate and the second fructose raw material have 50 Brix. 4. The method of preparation of claim 1 , wherein the fructose raffinate is treated by performing one or more step selected from the group consisting of cooling, pH adjustment, ion purification and concentration, before being recycled to the psicose conversion reaction. 5. The method of preparation of claim 4 , wherein the product treated by the ion purification has an electric conductivity of 0 to 15 μs/cm (microsiemens per centimeter). 6. The method of preparation of claim 1 , wherein the fructose raffinate obtained in the SMB chromatography separation process has an electric conductivity of 20 to 200 μs/cm (microsiemes per centimeter). 7. The method of preparation of claim 1 , wherein the method further comprises a step of ion purification step for adjusting the fructose raffinate in the mixture such that the mixture has an calcium ion concentration of 0.05 mM (millimolar) or lower, before being recycled to the psicose conversion reaction. 8. The method of preparation of claim 4 , wherein the cooling is performed by a step of cooling the fructose raffinate obtained in the SMB chromatography separation process with a heat exchanger. 9. The method of preparation of claim 1 , wherein the fructose content of fructose-containing raw material supplied to the psicose conversion reaction is 85 wt % or higher based on the 100 wt % of the total saccharides content in the fructose raffinate. 10. The method of preparation of claim 1 , wherein the fructose raffinate obtained in the SMB chromatography separation process contains 85 to 98 wt % of fructose content and 2.0 wt % or lower of psicose content, based on the 100 wt % of the total saccharides content in the fructose raffinate. 11. The method of preparation of claim 1 , wherein the method further comprises a step of adjusting a temperature, or controlling an input amount of fructose raffinate supplied to the psicose conversion reaction, after supplying the fructose raffinate into a storage tank. 12. The method of preparation of claim 1 , wherein the method further comprises a step of ion purification of the fructose raffinate (1) before, or after the SMB chromatography separation process, or (2) both before and after the SMB chromatography separation process. 13. The method of preparation of claim 1 , wherein the SMB chromatography separation process is carried out by a chromatographic column packed with a cation exchange resin having an attached calcium active group. 14. The method of preparation of claim 1 , wherein the psicose conversion reaction is performed by using a biological catalyst having a psicose conversion rate of 15% to 70%. 15. The method of preparation of claim 1 , wherein the method is performed continuously. 16. The method of preparation of claim 1 , wherein the method further comprises a step of concentrating the psicose fraction and crystallizing the psicose from the concentrated psicose fraction to obtain psicose crystal and crystallization mother liquor.

Assignees

Inventors

Classifications

  • Fructose (separation from invert sugar C13K3/00) · CPC title

  • Cation-exchange · CPC title

  • Intermediate storage of effluents · CPC title

  • placed in series · CPC title

  • B01D15/185Primary

    characterised by the components to be separated · CPC title

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What does patent US12024751B2 cover?
The present invention relates to a method for effectively utilizing fructose raffinate obtained in the process for separating psicose conversion product with a high purity chromatography in the process for preparing psicose, and more specifically, it is utilized for preparation of fructose-containing raw material solution for preparing psicose by supplying the fructose raffinate obtained in the…
Who is the assignee on this patent?
Samyang Corp
What technology area does this patent fall under?
Primary CPC classification B01D15/185. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Jul 02 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 4 related publications on this page (citations in our corpus or others sharing the same primary CPC).