[go: up one dir, main page]

GB675793A - Stabilized starch derivatives - Google Patents

Stabilized starch derivatives

Info

Publication number
GB675793A
GB675793A GB2624/50A GB262450A GB675793A GB 675793 A GB675793 A GB 675793A GB 2624/50 A GB2624/50 A GB 2624/50A GB 262450 A GB262450 A GB 262450A GB 675793 A GB675793 A GB 675793A
Authority
GB
United Kingdom
Prior art keywords
starch
beta
lactone
treated
per cent
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
Application number
GB2624/50A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NAT STARCH PRODUCTS Inc
Original Assignee
NAT STARCH PRODUCTS Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by NAT STARCH PRODUCTS Inc filed Critical NAT STARCH PRODUCTS Inc
Publication of GB675793A publication Critical patent/GB675793A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B31/00Preparation of derivatives of starch
    • C08B31/02Esters
    • C08B31/04Esters 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)

Abstract

Starch ethers and esters of poly-beta-hydroxy aliphatic acids are obtained by reacting starches with lactones of the acids. Alkaline reaction conditions give esters and neutral or acid conditions yield ethers (c.f. Group IV(b)). The term starch includes its conversion products or derivatives which contain free hydroxyl groups. Many lactones are specified, representative being beta propio-, isobutyro- and valero-lactone.ALSO:Starch reacted with an inner ester of a beta hydroxy aliphatic acid yields esters under alkaline conditions and ethers under neutral or acid conditions. Starch or its conversion products or derivatives which contain free hydroxyl groups may be used. Inner esters specified are beta-propio-, -butyro-, -isobutyro-, -valero- and -iso-valero-lactone. Room or higher temperatures may be used. The products form aqueous dispersions of substantially the same viscosity as those obtained from the untreated starch but retain their clarity and viscosity for longer. Desirably moisture is present during reaction, e.g. a minimum of approximately 10 per cent, based on dry weight of starch. Quantities of inner ester mentioned are 0.1 and 300 per cent of the weight of dry starch, higher proportions leading to a product which absorbs and swells in alcohols, e.g. glycerine and glycols. The lactone may react with the substituent of the starch to yield an ether or ester of a polyacid. The lactone may be added to an aqueous dispersion of the starch. Preferably the ratio of starch/water is not in excess of 5/1. Inorganic and organic alkalies are specified, preferably in amounts of 0.1-3 per cent of the starch. Large amounts of lactone, e.g. 10 per cent, are added at intervals as is the alkali so as to maintain a pH of about 10. The lactone may also be blended, e.g. by spraying, with an ordinary air-dry starch which may contain the alkali. In examples: (1) an ungelatinized thin-boiling corn starch, (2) tapioca British gum, (3) and (5) corn starch, and (4) thin-boiling potato starch are treated in aqueous caustic soda suspension with beta-propiolactone; (6) corn starch is made alkaline by treatment with sodium hydroxide, dried to a moisture content of 10-15 per cent, and treated by spraying with beta-propiolactone; (7) wheat starch suspended in aqueous caustic potash is treated with beta-butyro-lactone; (8) corn starch in aqueous suspension is treated with beta-propiolactone; and (9) corn starch is treated in hydrochloric acid suspension, pH 3.0, with beta-propiolactone. The products may be marketed as mixtures of the reactants, the reaction then taking place on addition to water.
GB2624/50A 1949-02-02 1950-02-01 Stabilized starch derivatives Expired GB675793A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US675793XA 1949-02-02 1949-02-02

Publications (1)

Publication Number Publication Date
GB675793A true GB675793A (en) 1952-07-16

Family

ID=22076974

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2624/50A Expired GB675793A (en) 1949-02-02 1950-02-01 Stabilized starch derivatives

Country Status (1)

Country Link
GB (1) GB675793A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8149655B2 (en) 2004-09-17 2012-04-03 Pioneer Corporation Information recording medium, information recording apparatus and method, information reproducing apparatus and method, and computer program

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8149655B2 (en) 2004-09-17 2012-04-03 Pioneer Corporation Information recording medium, information recording apparatus and method, information reproducing apparatus and method, and computer program

Similar Documents

Publication Publication Date Title
US2426125A (en) Manufacture of glycol alginates
US2517577A (en) Preparation of carboxyalkyl ethers of cellulose
US3375243A (en) Method of producing alkyl glucoside compositions
GB714701A (en) Improvements in or relating to a process for the production of starch derivatives and the resulting product
US3378546A (en) Hydroxypropyl starch ether
US2332048A (en) Preparation of water-soluble carboxyethyl cellulose ether
US4480091A (en) Process for preparing cellulose sulfate esters
US2698818A (en) Production of starch conversion products
GB912387A (en) A chemically modified starch and method of producing same
GB675793A (en) Stabilized starch derivatives
GB691364A (en) Polysaccharide derivatives of substituted dicarboxylic acids
US3033853A (en) Preparation of hydroxyalkyl starches
Nichols Jr et al. Allyl ether of starch
GB699530A (en) Foaming agents and processes for their production from starch or high polymeric starch derivatives
GB881371A (en) Water resistant adhesive comprising a gelatinized starch and process for preparing same
GB741742A (en) Improvements in or relating to preparation of starch ethers and the products resulting therefrom
US2609367A (en) Gum reaction product and processes
GB688291A (en) Starch product of improved properties and method of making the same
GB992213A (en) Cold water soluble adhesives
US2654736A (en) Stabilized starch derivatives
GB713750A (en) Ungelatinized cold water soluble starch ethers
GB343521A (en) Improvements in or relating to the manufacture of cellulose ethers
US3071573A (en) Method of preparing a starch carboxyl alkyl ether derivative
US2697094A (en) Fungicidal products of cellulose ethers
GB734924A (en) Improvements in or relating to modified ethyl cellulose and its method of preparation