GB631242A - Improvements in making of starch derivatives - Google Patents
Improvements in making of starch derivativesInfo
- Publication number
- GB631242A GB631242A GB2606146A GB2606146A GB631242A GB 631242 A GB631242 A GB 631242A GB 2606146 A GB2606146 A GB 2606146A GB 2606146 A GB2606146 A GB 2606146A GB 631242 A GB631242 A GB 631242A
- Authority
- GB
- United Kingdom
- Prior art keywords
- anhydride
- starch
- per cent
- anhydrides
- acetic
- 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
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
- C08B31/02—Esters
- C08B31/04—Esters of organic acids, e.g. alkenyl-succinated starch
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Paper (AREA)
Abstract
Ungelatinized starch derivatives are obtained by treating ungelatinized starch with a carboxylic acid anhydride in an aqueous alkaline medium of preferably pH 7 to 11. The derivatives show "non-gel," "increased water absorption" and "inhibited" characteristics depending on the quantity and type of anhydride used. In general, "non-gel" starches are obtained from acetic, propionic, butyric and phthalic anhydrides, "water absorptive" from succinic, maleic, glutaric and citraconic anhydrides these derivatives also having "non-gel" properties and inhibited starches from adipic and azelaic anhydrides. The starch used may be modified as by e.g. acid hydrolysis to yield "fluidity starches." Up to 10 per cent by weight of anhydride is preferred per weight of dry starch and alkalies mentioned are sodium, potassium and calcium hydroxides, sodium carbonate and tri-sodium phosphate. In the preferred method the anhydride is added to an aqueous alkaline suspension of ungelatinized starch. Other methods are the concurrent addition of aqueous alkali and anhydride to a starch milk; concurrent addition to the reaction vessel of aqueous alkali, anhydride and starch milk, heating a mixture of anhydride and commercially dry starch (containing about 5 to 20 per cent moisture) which has been treated with trisodium phosphate. Derivatives of anhydrides such as chloro-maleic anhydride may be used alone or mixed with anhydrides and acids such as citric acid may be used in conjunction with a dehydrating chemical such as acetic anhydride, acetyl chloride and thionyl chloride, in which case the corresponding acid anhydride is produced. The derivatives obtained may be after-treated as by e.g. chlorination with sodium hypochlorite solution. The products may be used as sizes in the textile and paper trades, and in the adhesive and food industries. In examples, "non - gelling" starches are produced by treating corn starch with 2 per cent sodium hydroxide solution and (1) and (2) acetic anhydride, (6) maleic anhydride followed by sodium hypochlorite and (7) phthalic anhydride, (3) by the concurrent addition of propionic anhydride and 3 per cent sodium hydroxide to corn starch milk, (4) and (5) from 20 fluidity starch by treatment with maleic and acetic anhydrides, (8) and (9) from corn starch by treatment with succinic anhydride and 3 per cent sodium hydroxide, sodium succinate formed being removed at the halfway stage because it buffers the reaction, (14) and (15) heating a mixture of corn starch with either acetic or succinic anhydride and trisodium phosphate, "water absorptive" by (7), (8), (9), (14), (15) and (10) from tapioca starch on treatment with chloro-maleic anhydride and 3 per cent sodium hydroxide, and "inhibited" by waxy maize starch and 3 per cent sodium hydroxide and (11) adipic anhydride, (12) mixed succinic and acetic anhydrides, (13) from high-grade tapioca starch with 3 per cent sodium hydroxide and adipic or citric acid in acetic anhydride and (16) by heating waxy-maize starch with adipic anhydride and trisodium phosphate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2606146A GB631242A (en) | 1946-08-29 | 1946-08-29 | Improvements in making of starch derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2606146A GB631242A (en) | 1946-08-29 | 1946-08-29 | Improvements in making of starch derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
GB631242A true GB631242A (en) | 1949-10-31 |
Family
ID=10237743
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2606146A Expired GB631242A (en) | 1946-08-29 | 1946-08-29 | Improvements in making of starch derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB631242A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4297144A (en) | 1975-07-22 | 1981-10-27 | Cpc International Inc. | High speed corrugating adhesives |
CN102702368A (en) * | 2012-05-08 | 2012-10-03 | 华南理工大学 | Mobile starch and dry-process preparation method thereof |
CN104262492A (en) * | 2014-09-22 | 2015-01-07 | 华南理工大学 | Preparation method of starch glutarate or modified starch glutarate |
CN109810288A (en) * | 2018-12-28 | 2019-05-28 | 东莞建泰生物科技有限公司 | A kind of crosslinking agent, preparation method and application |
CN112144302A (en) * | 2020-09-09 | 2020-12-29 | 浙江智兴集团有限公司 | Reactive dye dyeing process with high rubbing color fastness |
CN113058073A (en) * | 2021-03-16 | 2021-07-02 | 卫纳塞德(北京)医疗科技有限公司 | Cold compress type medical hydrogel and preparation method thereof |
CN113058072A (en) * | 2021-03-16 | 2021-07-02 | 卫纳塞德(北京)医疗科技有限公司 | Antibacterial medical cold compress hydrogel and preparation method thereof |
CN114272434A (en) * | 2021-03-16 | 2022-04-05 | 卫纳塞德(北京)医疗科技有限公司 | Degradable medical cold compress hydrogel and preparation method thereof |
-
1946
- 1946-08-29 GB GB2606146A patent/GB631242A/en not_active Expired
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4297144A (en) | 1975-07-22 | 1981-10-27 | Cpc International Inc. | High speed corrugating adhesives |
CN102702368A (en) * | 2012-05-08 | 2012-10-03 | 华南理工大学 | Mobile starch and dry-process preparation method thereof |
CN104262492A (en) * | 2014-09-22 | 2015-01-07 | 华南理工大学 | Preparation method of starch glutarate or modified starch glutarate |
CN109810288A (en) * | 2018-12-28 | 2019-05-28 | 东莞建泰生物科技有限公司 | A kind of crosslinking agent, preparation method and application |
CN112144302A (en) * | 2020-09-09 | 2020-12-29 | 浙江智兴集团有限公司 | Reactive dye dyeing process with high rubbing color fastness |
CN113058073A (en) * | 2021-03-16 | 2021-07-02 | 卫纳塞德(北京)医疗科技有限公司 | Cold compress type medical hydrogel and preparation method thereof |
CN113058072A (en) * | 2021-03-16 | 2021-07-02 | 卫纳塞德(北京)医疗科技有限公司 | Antibacterial medical cold compress hydrogel and preparation method thereof |
CN114272434A (en) * | 2021-03-16 | 2022-04-05 | 卫纳塞德(北京)医疗科技有限公司 | Degradable medical cold compress hydrogel and preparation method thereof |
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