WO2000031145A1 - Process for oxidising starch - Google Patents
Process for oxidising starch Download PDFInfo
- Publication number
- WO2000031145A1 WO2000031145A1 PCT/NL1999/000726 NL9900726W WO0031145A1 WO 2000031145 A1 WO2000031145 A1 WO 2000031145A1 NL 9900726 W NL9900726 W NL 9900726W WO 0031145 A1 WO0031145 A1 WO 0031145A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- carbohydrate
- process according
- hydrogen peroxide
- starch
- viscosity
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B31/00—Preparation of derivatives of starch
- C08B31/18—Oxidised starch
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
Definitions
- the invention relates to a process for lowering the viscosity of carbohydrates by oxidative degradation
- Starch must be subjected to a treatment to lower the viscosity before it can be used industrially
- the starch is generally subjected to oxidative treatment at elevated temperature (40-60 °C) in an alkaline medium
- oxidative treatment at elevated temperature (40-60 °C) in an alkaline medium
- hypochlorite is used as oxidising agent at 40 °C
- the reaction takes 4 - 15 hours
- the disadvantage of this method is the amount of salt formed and the extensive degradation of starch, accompanied by incorporation of chlorine
- virtually dry potato starch can be gelled by treatment with hydrogen peroxide at 45 °C for 6 hours
- Such a treatment is suitable for the preparation of blancmange, but the viscosity is too high and not stable for other applications.
- US-A 5,362,868 discloses a method according to which the viscosity of (hydroxy- ethyl)starch is lowered by oxidation with a per-acid
- the per-acid used is, for example, peroxysulphuric acid (H 2 SOs) or peracetic acid
- the peroxysulphuric acid has to be prepared in situ from hydrogen peroxide and sulphuric acid
- the reactivity of peracetic acid is lower and leads to longer reaction times It is also described in US-A 5,362,868 that reaction with hydrogen peroxide leads to unacceptable reaction times
- the viscosity of starch and other carbohydrates can be lowered by treatment with hydrogen peroxide in the presence of an acylated carbohydrate
- the aim of the invention is to provide a method for lowering the viscosity of starch and other carbohydrates using simple reagents, without the use of heavy metals and salt- forming reagents, and without organic by-products
- a stable viscosity is obtained, that is to say a stability which does not increase further at ambient temperature
- Said aim is achieved by means of a method wherein the carbohydrate is oxidised with hydrogen peroxide in the presence of a catalyst and, after it lias been brought into contact with the hydrogen peroxide, the carbohydrate is, if necessary, dried at a temperature below 60 °C and is then treated at a temperature of 80 - 140 °C
- the process according to the invention is an inexpensive method with short reaction times and with low consumption of hydrogen peroxide, consumption being approximately 5 times as low as with the method according to WO 97/31951. There is also no salt burden or other waste stream worthy of mention.
- the method leads in high yield and with little loss to a soluble or dispersible carbohydrate, the solution or dispersion of which has a low and stable viscosity.
- Any polysaccharide that is completely or partially soluble in water can be used as the carbohydrate that can be treated in accordance with the process according to the invention.
- Such polysaccharides include, firstly, starch and fractions and derivatives thereof, such as amylose, ethoxylated starch and carboxymethylstarch.
- starch and fractions and derivatives thereof such as amylose, ethoxylated starch and carboxymethylstarch.
- solubility of cellulose and chitin and derivatives thereof can be improved, or the viscosity thereof can be lowered, by means of the method according to the invention.
- the quantity of hydrogen peroxide to be used is entirely dependent on the desired degree of oxidation. By virtue of the higher efficiency of the method according to the invention, a limited quantity of hydrogen peroxide can suffice.
- a solution of 0.1 - 20 % (m/m) hydrogen peroxide, preferably of 1 - 10 % (m/m) is used.
- the quantity and concentration of hydrogen peroxide taken is such that the carbohydrate does not dissolve to a significant extent and, in the case of starch, remains in granular form.
- the catalyst can be an organic acid, such as acetic acid, formic acid, propionic acid, lactic acid, oxalic acid, citric acid, succinic acid or an anhydride such as acetic anhydride, and in particular a cyclic anhydride of a dicarboxylic acid such as succinic anhydride, maleic anhydride or citraconic anhydride, or possibly a lactone or lactide. Phosphoric acid can also be used.
- the quantity of catalyst is, for example, 0.1 - 4 % (m/m), in particular 0.5 - 2 % (m m), with respect to the carbohydrate. After hydrogen peroxide and catalyst have been added and mixed, the undissolved carbohydrate is filtered off if necessary.
- the water content must not be too high for the following step. If the water content is more than 20 or 25 % (with respect to the mass of the carbohydrate and water), the carbohydrate is then dried. Drying is carried out at a temperature of at most 60, and in particular below 55 °C, down to, for example, ambient temperature, to a water content of at most 25 % (m/m), in particular of 15-20 % (m/m), with respect to the carbohydrate. In the case of starch, drying must be carried out under conditions such that the starch does not gelatinise or barely gelatinises. Drying drums can optionally be used for drying on a large scale.
- the dried carbohydrate is then kept at a temperature above 80 °C, in particular above 100 °C, up to about 140 °C, for a period of at least 10 minutes, in particular for a period of 1 - 10 hours, during which period the actual oxidation takes place
- a temperature above 80 °C in particular above 100 °C, up to about 140 °C
- a period of at least 10 minutes in particular for a period of 1 - 10 hours, during which period the actual oxidation takes place
- higher temperature for example 120 °C
- use can be made of fluidised beds, microwave ovens and the like It is important that an open reactor is used, so that any residual water released can be removed easily If the residual water is not adequately removed, the carbohydrate, in the case of starch, can then still gelatinise
- the viscosity of the carbohydrate of reduced viscosity that is obtained using the method according to the invention can be determined using a Brabender viscometer According to the measurement method, a 25 % (m/m) solution or suspension is heated from 40 °C at a rate of 1 5 °C/min, during this heating the viscosity initially rises to a maximum (peak viscosity), on further heating the viscosity falls again, at 90 °C the temperature is not raised further and the viscosity reaches a minimum (valley viscosity), after 30 min at 90 °C cooling is carried out, again at a rate of 1 5 °C/min, to a final temperature of 40 °C, the viscosity at this end point is termed the final viscosity
- the product according to the invention preferably has a peak, valley and final viscosity of 4,000, 200 and 2,000, respectively, with 2,000, 100 and 500 Brabender units, respectively, being most preferred, with a minimal reduction in the
- a quantity of potato starch (100 - 1000 g) is suspended in a solution of 5 % or 2 5 % hydrogen peroxide in water Acetic acid or maleic anhydride is optionally added After filtration, the material filtered off contains 30-40 % water, the hydrogen peroxide content is therefore about 1 % (m/m) at 2 5 % H 2 O 2
- the filter cake is dried in air for three days instead of this it is also possible to dry for a few hours under a stream of air at approximately 50 °C
- the powder obtained is then kept at 120 °C in an oven for a number of hours (reaction time)
- the material obtained is white and has retained its granular structure
- the number of carboxylic acid groups is approximately 1 per 57 anhydroglucose units Brabender curves were recorded for the materials (25 % in water) at pH 7 0
- Table 1 Table 1
- AA acetic acid
- MA maleic anhydride percentage by weight in water viscosity too high to be able to be measured 4 after 30 minutes at 40 °C: 108 wheat starch
- a quantity of potato starch (100 - 1000 g) is dried to a moisture content of at most 10 %.
- 2.5 % H 2 O 2.5 gram per 100 gram dry starch, 100 % solids
- 1 % or 0.5 % or 0.25 % acetic acid (with respect to dry starch)
- 1.0 % or 0.5 % maleic anhydride (with respect to dry starch)
- the peroxide, acetic acid and maleic anhydride are all dissolved in water.
- the total quantity of water water already present in the starch plus water added via the chemicals) is, however, no greater than 20 % (solids content of 80 %).
- the whole is mixed well in order then to react for 3 hours at 120 °C.
- the material obtained is white and has retained its granular structure. Brabender curves were recorded for the materials (25 % in water) at pH 7.0. The results are given in Table 2 below. Table 2
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL99347895A PL347895A1 (en) | 1998-11-26 | 1999-11-26 | Process for oxidising starch |
AU14172/00A AU1417200A (en) | 1998-11-26 | 1999-11-26 | Process for oxidising starch |
JP2000583969A JP2002530487A (en) | 1998-11-26 | 1999-11-26 | Starch oxidation method |
EP99972649A EP1133524A1 (en) | 1998-11-26 | 1999-11-26 | Process for oxidising starch |
CA002352222A CA2352222A1 (en) | 1998-11-26 | 1999-11-26 | Process for oxidising starch |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL1010660A NL1010660C2 (en) | 1998-11-26 | 1998-11-26 | Method for oxidizing starch. |
NL1010660 | 1998-11-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000031145A1 true WO2000031145A1 (en) | 2000-06-02 |
Family
ID=19768210
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/NL1999/000726 WO2000031145A1 (en) | 1998-11-26 | 1999-11-26 | Process for oxidising starch |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP1133524A1 (en) |
JP (1) | JP2002530487A (en) |
CN (1) | CN1328572A (en) |
AU (1) | AU1417200A (en) |
CA (1) | CA2352222A1 (en) |
NL (1) | NL1010660C2 (en) |
PL (1) | PL347895A1 (en) |
WO (1) | WO2000031145A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003025021A1 (en) * | 2001-09-19 | 2003-03-27 | Degussa Ag | Method for oxidizing starch |
US6887496B2 (en) | 2001-12-20 | 2005-05-03 | Kimberly-Clark Worldwide, Inc. | Products for controlling microbial organic compound production |
CN102212143A (en) * | 2011-05-17 | 2011-10-12 | 东华大学 | Pollution-free preparation method for oxidized phosphated double-modified starch |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3205673B1 (en) * | 2016-02-12 | 2018-05-23 | Coöperatie Avebe U.A. | Oxidation of starch |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3975206A (en) * | 1974-11-18 | 1976-08-17 | A. E. Staley Manufacturing Company | Method of peroxide thinning granular starch |
WO1997031951A1 (en) * | 1996-02-29 | 1997-09-04 | Kemira Chemicals B.V. | Process for oxidising starch |
-
1998
- 1998-11-26 NL NL1010660A patent/NL1010660C2/en not_active IP Right Cessation
-
1999
- 1999-11-26 AU AU14172/00A patent/AU1417200A/en not_active Abandoned
- 1999-11-26 WO PCT/NL1999/000726 patent/WO2000031145A1/en not_active Application Discontinuation
- 1999-11-26 CA CA002352222A patent/CA2352222A1/en not_active Abandoned
- 1999-11-26 PL PL99347895A patent/PL347895A1/en not_active Application Discontinuation
- 1999-11-26 JP JP2000583969A patent/JP2002530487A/en active Pending
- 1999-11-26 EP EP99972649A patent/EP1133524A1/en not_active Withdrawn
- 1999-11-26 CN CN99813802A patent/CN1328572A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3975206A (en) * | 1974-11-18 | 1976-08-17 | A. E. Staley Manufacturing Company | Method of peroxide thinning granular starch |
WO1997031951A1 (en) * | 1996-02-29 | 1997-09-04 | Kemira Chemicals B.V. | Process for oxidising starch |
Non-Patent Citations (3)
Title |
---|
DATABASE CAS STN; 1972, "Dry process for the modification of starch", XP002109992 * |
DATABASE CAS STN; 1985, "Production of modified starch products with hydrogen peroxide and IR heating", XP002109993 * |
KUZNETSOVA I.I. ET AL., SAKH. PROM-ST, no. 9, 1984, pages 47 - 50 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003025021A1 (en) * | 2001-09-19 | 2003-03-27 | Degussa Ag | Method for oxidizing starch |
US6887496B2 (en) | 2001-12-20 | 2005-05-03 | Kimberly-Clark Worldwide, Inc. | Products for controlling microbial organic compound production |
US7235263B2 (en) | 2001-12-20 | 2007-06-26 | Kimberly-Clark Worldwide, Inc. | Processes for controlling microbial organic compound production |
CN102212143A (en) * | 2011-05-17 | 2011-10-12 | 东华大学 | Pollution-free preparation method for oxidized phosphated double-modified starch |
Also Published As
Publication number | Publication date |
---|---|
PL347895A1 (en) | 2002-04-22 |
CA2352222A1 (en) | 2000-06-02 |
EP1133524A1 (en) | 2001-09-19 |
AU1417200A (en) | 2000-06-13 |
JP2002530487A (en) | 2002-09-17 |
CN1328572A (en) | 2001-12-26 |
NL1010660C2 (en) | 2000-05-30 |
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