GB537009A - Manufacture of synthetic resins - Google Patents

Manufacture of synthetic resins

Info

Publication number
GB537009A
GB537009A GB26886/39A GB2688639A GB537009A GB 537009 A GB537009 A GB 537009A GB 26886/39 A GB26886/39 A GB 26886/39A GB 2688639 A GB2688639 A GB 2688639A GB 537009 A GB537009 A GB 537009A
Authority
GB
United Kingdom
Prior art keywords
urea
heated
aqueous formaldehyde
isobutanol
product
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
GB26886/39A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB537009A publication Critical patent/GB537009A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

537,009. Polyamide-aldehyde condensation products ; treated fabrics ; dyeing. DU PONT DE NEMOURS & CO., E.I. Sept. 29, 1939, No. 26886. Convention date, Sept. 30, 1938. [Classes 2 (iii) and 15 (ii)] [Also in Group VIII] Synthetic resins are prepared by heating a polyamide-forming material as described in Specifications 461,236, 461,237 and 474,999 (a mixture of diamine and dicarboxylic. acid, a diamine dibasic acid salt or a monoaminomonocarbonylic amine) with a urea to form a low molecular weight polymer and treating the condensate with an aldehyde, the quantity of urea employed being at least 0.5 molecules per molecule of polymethylene di ammonium salt present or potentially present in the polyamide. The reaction with aldehyde is preferably effected in the presence of an alcohol. The term " urea includes urea and its equivalents in resin-formation with aldehydes such as thiourea, ammonium isocyanate, ammonium isothiocyanate, biuret, cyanamide, guanidine, guanidine isocyanate, guanidine carbonate, ammonium carbonate, and dicyanadiamide. Suitable diamines include tetra-, penta-, hexa-, and octamethylene diamine, p-xylylenediamine, triglycoldiamine, diaminoisopropanol and diethylenetriamine; suitable acids include glutaric, adipic, pimelic, suberic, lutidinic, sebacic, methyladipic, p-phenylenediacetic, terephthalic and isophthalic acids ; suitable aminoacids or lactams include 6-aminocaproic, 9-aminonon- anoic and 11-aminoundecanoic acids and caprolactam ; the diamines and dicarboxylic acids are preferably used as salts. In examples hexamethylene diammonium adipate and urea are heated and the product reacted (1) with a solution of urea in isobutanol and aqueous formaldehyde, (2) with a solution of aqueous formaldehyde in isobutanol or methanol, (4) with aqueous formaldehyde ; (7) hexamethylene diammonium adipate and urea are heated in the presence of m-cresol, the product being reacted with aqueous formaldehyde in the presence of ethanol; (8) hexamethylenediammonium adipate is heated with urea and the product, after refluxing with isobutanol is reacted with formaldehyde; (10) decamethylenediammonium sebacate is heated with urea and the product heated with a solution of aqueous formaldehyde in isobutanol; (11) hexamethylenediammonium isophthalate is heated with urea and the product heated with a solution of aqueous formaldehyde in isobutanol. The products may be used in the manufacture of coating compositions, moulding powders and films which are readily dyed by silk or wool dyes. Fabrics impregnated with dilute solutions of the resin and baked are rendered crease-resistant and water-repellent and their affinity for silk and wool dyes is increased. The resins may be plasticized by castor oil modified alkyl resins. They may be used as top-coatings over nitro-cellulose coated fabrics. U.S.A. Specifications 2,071,250 and 2,130,948 are referred to.
GB26886/39A 1938-09-30 1939-09-29 Manufacture of synthetic resins Expired GB537009A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US537009XA 1938-09-30 1938-09-30

Publications (1)

Publication Number Publication Date
GB537009A true GB537009A (en) 1941-06-05

Family

ID=21985963

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26886/39A Expired GB537009A (en) 1938-09-30 1939-09-29 Manufacture of synthetic resins

Country Status (1)

Country Link
GB (1) GB537009A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4410652A (en) * 1980-02-22 1983-10-18 Sandoz Ltd. Reaction products useful for improving the wetfastness of direct and reactive dyes on cellulosic substrates

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4410652A (en) * 1980-02-22 1983-10-18 Sandoz Ltd. Reaction products useful for improving the wetfastness of direct and reactive dyes on cellulosic substrates

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