WO2005065655A2 - Verfahren zur herstellung von keto-l-gulonsäuresprühgranulaten - Google Patents
Verfahren zur herstellung von keto-l-gulonsäuresprühgranulaten Download PDFInfo
- Publication number
- WO2005065655A2 WO2005065655A2 PCT/EP2004/014824 EP2004014824W WO2005065655A2 WO 2005065655 A2 WO2005065655 A2 WO 2005065655A2 EP 2004014824 W EP2004014824 W EP 2004014824W WO 2005065655 A2 WO2005065655 A2 WO 2005065655A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- keto
- gulonic acid
- fluidized bed
- drying
- spray
- 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.)
- Ceased
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1682—Processes
- A61K9/1688—Processes resulting in pure drug agglomerate optionally containing up to 5% of excipient
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/191—Carboxylic acids, e.g. valproic acid having two or more hydroxy groups, e.g. gluconic acid
Definitions
- the present invention relates to a process for the preparation of keto-L-gulonic acid spray granules.
- Keto-L-gulonic acid is an important intermediate in the production of ascorbic acid (vitamin C).
- crystalline keto-L-gulonic acid is produced via the process steps of the fermentative production of sodium ketogulonate, cell separation, ion exchange chromatography, evaporation and crystallization.
- keto-L-gulonic acid spray granules from finely divided, pure keto-L-gulonic acid by using an aqueous or water-containing solution of keto-L-gulonic acid a) a spray fluidized-bed drying, b) a single-component atomization drying or c) a spray drying Sputtering drying supplies.
- the process according to the invention is particularly advantageous if the aqueous or water-containing solution of pure keto-L-gulonic acid is fed to a fluidized-bed dryer.
- keto-L-gulonic acid as is available in the prior art, is used as the starting material for the process according to the invention.
- Keto-L-gulonic acid which has been produced in a fermentative process, is used particularly advantageously.
- the aqueous or water-containing solution of the pure keto-L-gulonic acid usually contains 10 to 80% by weight, preferably 40 to 70% by weight of keto-L-gulonic acid.
- water-miscible solvents include, for example, alkanols with a chain length of 1 to 4 carbon atoms.
- Pure keto-L-gulonic acid is hereinafter referred to as a keto-L-gulonic acid with a degree of purity of higher than 95%, preferably 98 or 99%.
- the solution is sprayed continuously or discontinuously into a fluidized bed of dry reaction product in the spray fluidized bed drying according to the invention.
- keto-L-gulonic acid in the form of a keto-L-gulonic acid dry powder is placed in a fluidized bed dryer in a fluidized bed kept at 50 to 150 ° C., for this purpose adds the aqueous or water-containing solution of keto-L-gulonic acid in sprayed form in accordance with the drying rate, removes the keto-L-gulonic acid particles from the fluidized bed after a suitable dwell time and separates them into particle fractions by means of a suitable device, which removes the particle fraction in the particle size range of approximately and returns the finely divided particles and / or the coarser particles to the granulation process, if necessary after comminution.
- the spray fluidized bed drying can be carried out batchwise or continuously, but the continuous mode of operation is preferred.
- keto-L-gulonic acid product To carry out the process, such a keto-L-gulonic acid product must first be produced from dry keto-L-gulonic acid powder, with the aid of which a fluidized bed can be produced. In the case of discontinuous operation, a relatively fine-particle product can be placed in the fluidized bed. Depending on the residence time of the particles in the fluidized bed, a dry product with a smaller or larger particle size range is then obtained. Particles in the size range from 50 to 1000 ⁇ m, preferably 100 to 500 ⁇ m, have the desired handling properties and are therefore obtained as a valuable product. Smaller particles and keto-L-gulonic acid product obtained by suitable grinding, for example grinding larger particles, are used as fluidized bed material for further batches.
- the aqueous or water-containing solution of keto-L-gulonic acid is sprayed continuously into a fluidized bed.
- the rate of spraying is adjusted so that the fluidized bed has a temperature corresponding to the desired degree of drying. Accordingly, it is ultimately determined by the difference between the inlet and outlet temperatures of the fluidizing gas. If the process is carried out continuously, the first time the fluidized bed dryer is started up, fine-particle keto-L-gulonic acid in the fluidized bed is assumed. Then you get a dry product with an almost constant particle size ratio. A certain part of this is continuously removed and separated into particle size fractions.
- Customary binders for the spray fluidized-bed drying process according to the invention can also be added to the keto-L-gulonic acid, but the embodiment without the addition of binders is preferred.
- keto-L-gulonic acid An aqueous solution containing 50% by weight of keto-L-gulonic acid was placed in a laboratory stirred tank, heated to approx. 45 ° C. and continuously pumped into the Miniplant spray vortex dryer under the in Boundary conditions listed in Table 1 injected.
- the solid produced was continuously discharged. This resulted in 8.5 kg of free-flowing, dust-free keto-L-gulonic acid granules with a residual moisture content of ⁇ 0.5% by weight and the following particle size distribution: 91% ⁇ 900 ⁇ m, 9%> 900 ⁇ m
- aqueous solution with 35% by weight of keto-L-gulonic acid was placed in a stirred tank and heated to about 35 to 40 ° C. With the help of a peristaltic pump, the solution was continuously injected into the pilot plant spray vortex dryer under the boundary conditions listed in Table 1 over a period of 18 hours.
- the solid produced was continuously discharged. This resulted in 320 kg of free-flowing, dust-free keto-L-gulonic acid granulate with a residual moisture content of ⁇ 0.5% by weight and the following particle size distribution:
Landscapes
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04804409A EP1703897A2 (de) | 2004-01-05 | 2004-12-30 | Verfahren zur herstellung von keto-l-gulonsäuresprühgranulaten |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004001187.7 | 2004-01-05 | ||
| DE200410001187 DE102004001187A1 (de) | 2004-01-05 | 2004-01-05 | Verfahren zur Herstellung von Keto-L-gulonsäuresprühgranulaten |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2005065655A2 true WO2005065655A2 (de) | 2005-07-21 |
| WO2005065655A3 WO2005065655A3 (de) | 2005-11-03 |
Family
ID=34716328
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2004/014824 Ceased WO2005065655A2 (de) | 2004-01-05 | 2004-12-30 | Verfahren zur herstellung von keto-l-gulonsäuresprühgranulaten |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP1703897A2 (de) |
| DE (1) | DE102004001187A1 (de) |
| WO (1) | WO2005065655A2 (de) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103110105A (zh) * | 2012-11-14 | 2013-05-22 | 江苏江山制药有限公司 | 食品添加剂无糖维生素c钠盐颗粒的生产方法 |
| CN108774125A (zh) * | 2018-05-28 | 2018-11-09 | 苏州澄江环境科技有限公司 | 一种从古龙酸母液中回收原料的工艺 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102008045739B4 (de) | 2008-09-04 | 2021-12-30 | ABUS August Bremicker Söhne Kommanditgesellschaft | Schließzylindersystem |
| CN107473959B (zh) * | 2017-08-30 | 2021-03-12 | 沈阳农业大学 | 一种维生素c生产中的古龙酸减排提取法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5268283A (en) * | 1990-10-05 | 1993-12-07 | Miles Inc. | Method for the production of detergent builder formulations utilizing spray granulated citric acid and salts thereof |
| ATE289355T1 (de) * | 1995-12-27 | 2005-03-15 | Genencor Int | Verfahren zur herstellung von gluconsäure und durch dieses hergestellte gluconsäure |
| US6187570B1 (en) * | 1998-05-26 | 2001-02-13 | The Electrosynthesis Company, Inc. | Electrodialysis methods for purification and recovery of gluconic acid derivatives |
| KR20020019598A (ko) * | 1999-08-03 | 2002-03-12 | 추후제출 | 유기산의 회수 방법 |
-
2004
- 2004-01-05 DE DE200410001187 patent/DE102004001187A1/de not_active Withdrawn
- 2004-12-30 WO PCT/EP2004/014824 patent/WO2005065655A2/de not_active Ceased
- 2004-12-30 EP EP04804409A patent/EP1703897A2/de not_active Withdrawn
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103110105A (zh) * | 2012-11-14 | 2013-05-22 | 江苏江山制药有限公司 | 食品添加剂无糖维生素c钠盐颗粒的生产方法 |
| CN108774125A (zh) * | 2018-05-28 | 2018-11-09 | 苏州澄江环境科技有限公司 | 一种从古龙酸母液中回收原料的工艺 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1703897A2 (de) | 2006-09-27 |
| DE102004001187A1 (de) | 2005-08-04 |
| WO2005065655A3 (de) | 2005-11-03 |
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