GB772479A - A process for the manufacture of dry, cold-water-soluble binding agents, adhesives, finishing agents and the like from starch, a urea and an aldehyde - Google Patents

A process for the manufacture of dry, cold-water-soluble binding agents, adhesives, finishing agents and the like from starch, a urea and an aldehyde

Info

Publication number
GB772479A
GB772479A GB8819/53A GB881953A GB772479A GB 772479 A GB772479 A GB 772479A GB 8819/53 A GB8819/53 A GB 8819/53A GB 881953 A GB881953 A GB 881953A GB 772479 A GB772479 A GB 772479A
Authority
GB
United Kingdom
Prior art keywords
urea
starch
mixture
starches
water
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
GB8819/53A
Inventor
Jan Lolkema
Willem Albertus Van Der Meer
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.)
Scholtens Chemische Fabrieken NV
Original Assignee
Scholtens Chemische Fabrieken NV
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
Priority to BE527719D priority Critical patent/BE527719A/xx
Application filed by Scholtens Chemische Fabrieken NV filed Critical Scholtens Chemische Fabrieken NV
Priority to GB8819/53A priority patent/GB772479A/en
Priority to FR1097497D priority patent/FR1097497A/en
Publication of GB772479A publication Critical patent/GB772479A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L3/00Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
    • C08L3/02Starch; Degradation products thereof, e.g. dextrin
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J103/00Adhesives based on starch, amylose or amylopectin or on their derivatives or degradation products
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

A dry cold-water-soluble product is made by heating a mixture of disintegrated starch which may be esterified or etherified, water and either urea or an analogue thereof and an aldehyde or a precondensate thereof, while at the same time the mixture is pressed or spread out to a thin layer which is dried simultaneously or immediately thereafter. The disintegrated starches used are those of which a 15 per cent solution has a viscosity of at most 100 c.p. at 90 DEG C., e.g. dextrins, British gums and highly modified thin boiling starches. The urea-formaldehyde condensate may be etherified and/or esterified. Specified analogues of urea are thiourea, guanidine and glucoseureide. Part of the disintegrated starch may be pretreated with a urea and/or an aldehyde. The products may be used as thickening agents for rendering fabrics crease-resistant, abrasion-resistant or slip-free and to fix the pile thereof; for fixing pigments on textiles; as adhesives; for sizing paper; as a thickening and fixing agent in paper and textile printing; as a binding agent for powdered, granular or fibrous material (e.g. primings, cements, water colours, briquettes, foundry cores and fibre boards); or as a moulding material mixed with wood flour, bentonite, ground slate, asbestos, cellulose fibres, or fabric cuttings. Hardening of the product is effected with an acid or acid-producing substance. Water-soluble polysaccharides, e.g. cellulose ethers, may be added prior to, during or after the heating process. The products may be combined with other starch products, e.g. natural starches, thin boiling starches, dextrins, coldswelling starches, or cold-swelling starch ethers or esters. In examples: (1) a mixture of dextrin, dimethylol urea (or a mixture of 1 mol. of urea and 2 mols. of formaldehyde) of pH 5-11 is heated on a rotating cylinder to 130 DEG C. (2) A mixture of thin boiling starch and dimethylol urea or its dimethyl ether of pH 8 is heated on a rotating cylinder to 130-140 DEG C. (3) A mixture of an etherified disintegrated starch and dimethylol urea or its dimethyl ether of pH8 is heated on a rotating cylinder at 140 DEG C. (4) A urea-formaldehyde condensate is made by heating urea with formalin at pH 4 1/2 -5 and neutralizing with caustic soda; the condensate is then heated with dextrin as in Example (1). Specifications 494,927, [Group IV], 601,374, [Group IV (b)], 632,789 and 632,791, [Group IV (c)], are referred to.ALSO:A dry cold-water-soluble product is made by heating a mixture p of disintegrated starch which may be esterified or etherified water and either a urea and an aldehyde or a urea-aldehyde condensate to gelatinize the starch, while at the same time the mixture is pressed or spread out to a thin layer which is dried simultaneously or immediately thereafter. The disintegrated starches used are those of which a 15 per cent solution has a viscosity of at most 100 c.p. at 90 DEG C., elgl dextrins, British gums and highly modified thin-boiling starches. The urea-aldehyde condensate may be etherified and/or esterified. Specified ureas are urea, thiourea, guanidine and glucoseureide. Part of the disintegrated starch may be pretreated with a urea and/or an aldehyde. The products may be used as thickening agents for rendering fabrics crease-resistant, abrasion-resistant or slip free and to fix the pile thereof; for fixing pigments on textiles; as adhesives; for sizing paper; as a thickening and fixing agent in paper and textile printing; as a binding agent for powdered, granular or fibrous material (e.g. primings, cements, water colours, briquettes, foundry cores and fibre boards); or as a moulding material mixed with wood flour, bentonite, ground slate, asbestos, cellulose fibres or fabric cuttings. Hardening of the product is effected with an acid or acid-producing substance. Water-soluble polysaccharides e.g. cellulose ethers may be added prior to, during or after the heating process. The products may be combined with other starch products e.g. natural starches, thin-boiling starches, cold-swelling starches, or cold-swelling starch ethers or esters. In examples (1) a mixture of dextrin, dimethylol urea (or a mixture of 1 mil of urea and 2 mols of formaldehyde) of pH 5-11 is heated in a rotating cylinder to 130 DEG C. (2) A mixture of thin-boiling starch and dimethylol urea or its dimethyl ether of pH 8 is heated on a rotating cylinder to 130 DEG -140 DEG C. (3) A mixture of an etherified disintegrated starch and dimethylol urea or its dimethyl ether of pH 8 is heated on a rotating cylinder at 140 DEG C. (4) A urea formaldehyde condensate is made by heating urea with formalin at pH 4 1/2 -5 and neutralising with caustic soda; the condensate is then heated with dextrin as in Ex. (1). Specifications 494,927, 601,374, 632,789 and 632,791 are referred to.
GB8819/53A 1953-03-31 1953-03-31 A process for the manufacture of dry, cold-water-soluble binding agents, adhesives, finishing agents and the like from starch, a urea and an aldehyde Expired GB772479A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
BE527719D BE527719A (en) 1953-03-31
GB8819/53A GB772479A (en) 1953-03-31 1953-03-31 A process for the manufacture of dry, cold-water-soluble binding agents, adhesives, finishing agents and the like from starch, a urea and an aldehyde
FR1097497D FR1097497A (en) 1953-03-31 1954-03-31 Process for the manufacture of binders, adhesives, sizing or sizing agents and the like, soluble in cold water

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB8819/53A GB772479A (en) 1953-03-31 1953-03-31 A process for the manufacture of dry, cold-water-soluble binding agents, adhesives, finishing agents and the like from starch, a urea and an aldehyde

Publications (1)

Publication Number Publication Date
GB772479A true GB772479A (en) 1957-04-17

Family

ID=9859826

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8819/53A Expired GB772479A (en) 1953-03-31 1953-03-31 A process for the manufacture of dry, cold-water-soluble binding agents, adhesives, finishing agents and the like from starch, a urea and an aldehyde

Country Status (3)

Country Link
BE (1) BE527719A (en)
FR (1) FR1097497A (en)
GB (1) GB772479A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2999032A (en) * 1958-01-29 1961-09-05 Vasco Ind Corp Process for the preparation of amylose solutions
US3155527A (en) * 1962-06-21 1964-11-03 Corn Products Co Adhesive and method of preparation
US3222199A (en) * 1962-05-04 1965-12-07 Nat Starch Chem Corp Stabilization of amylose
US3284381A (en) * 1962-05-14 1966-11-08 Nat Starch Chem Corp Amylose-based corrugating adhesives
US3300330A (en) * 1962-10-09 1967-01-24 Johnson & Johnson Carrier sheet containing on opposite sides a formaldehyde modified starch release coating and a formaldehyde modified starch tacky coating
GB2172006A (en) * 1983-11-01 1986-09-10 Freunt Ind Co Ltd Excipient composition
WO2005052256A2 (en) * 2003-11-21 2005-06-09 Bercen Incorporated Paper making process and starch compositions comprising a crosslinking agent for use in same
CN109181577A (en) * 2018-09-25 2019-01-11 安溪县斯马拓科技发展有限公司 A kind of mongolicum Turcz. with Modified Starch Adhesive preparation process

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2999032A (en) * 1958-01-29 1961-09-05 Vasco Ind Corp Process for the preparation of amylose solutions
US3222199A (en) * 1962-05-04 1965-12-07 Nat Starch Chem Corp Stabilization of amylose
US3284381A (en) * 1962-05-14 1966-11-08 Nat Starch Chem Corp Amylose-based corrugating adhesives
US3155527A (en) * 1962-06-21 1964-11-03 Corn Products Co Adhesive and method of preparation
US3300330A (en) * 1962-10-09 1967-01-24 Johnson & Johnson Carrier sheet containing on opposite sides a formaldehyde modified starch release coating and a formaldehyde modified starch tacky coating
GB2172006A (en) * 1983-11-01 1986-09-10 Freunt Ind Co Ltd Excipient composition
WO2005052256A2 (en) * 2003-11-21 2005-06-09 Bercen Incorporated Paper making process and starch compositions comprising a crosslinking agent for use in same
WO2005052256A3 (en) * 2003-11-21 2005-09-15 Bercen Inc Paper making process and starch compositions comprising a crosslinking agent for use in same
CN109181577A (en) * 2018-09-25 2019-01-11 安溪县斯马拓科技发展有限公司 A kind of mongolicum Turcz. with Modified Starch Adhesive preparation process

Also Published As

Publication number Publication date
BE527719A (en) 1900-01-01
FR1097497A (en) 1955-07-06

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