GB344872A - Moulding compositions and moulded articles made therefrom - Google Patents

Moulding compositions and moulded articles made therefrom

Info

Publication number
GB344872A
GB344872A GB31010/29A GB3101029A GB344872A GB 344872 A GB344872 A GB 344872A GB 31010/29 A GB31010/29 A GB 31010/29A GB 3101029 A GB3101029 A GB 3101029A GB 344872 A GB344872 A GB 344872A
Authority
GB
United Kingdom
Prior art keywords
products
formaldehyde
moulding
materials
mols
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
GB31010/29A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Publication of GB344872A publication Critical patent/GB344872A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G12/00Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/04Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
    • C08G12/10Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with acyclic compounds having the moiety X=C(—N<)2 in which X is O, S or —N
    • C08G12/12Ureas; Thioureas

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

In the manufacture of moulding compositions comprising fibrous materials and a mixed condensation product of urea and thiourea with formaldehyde, the condensation product is prepared by condensing a sum of 2 mols. of urea and thiourea jointly with less than 4 mols. of formaldehyde in a medium having a hydrion concentration greater than pH 5, preferably pH 3, and heating the reaction mixture until a hydrophobe product is obtained. The products form stable sols. in the heat, thereby by facilitating their incorporation with the fibrous materials; the latter may, however, be present ab initio. The urea and the thiourea may be condensed simultaneously with formaldehyde, or one component may be added after the other has been preliminarily condensed, but the desired products are not obtainable by condensing one of the components almost completely with formaldehyde and then adding the other, or by mixing together condensation products separately obtained. Opaque products are prepared by briefly heating urea (1 mol.) with aqueous formaldehyde (1,5 mols.) in an acid medium as stated above, and then adding thiourea (1 mol.) and formaldehyde (1,5 mols.) with continued heating. Transparent products are obtained by adding urea (1 mol.) to a hot acid solution of thiourea (1 mol.) in aqueous formaldehyde (3 mols.) with continued heating. The hot solutions, after mixing with the fibrous materials, are dried, first in the air and then by heat, e.g. at 90-100 DEG C. Drying may be effected on heated rolls or in a rotary drum, and at atmospheric or reduced pressure. The products may then be ground and finally heated until a sample loses about 5 per cent of its weight when heated at 100 DEG C. They are then ready for moulding, the small amount of residual water being necessary to ensure sufficient fluidity. Moulding is effected at 140-180 DEG C. at 150-300 kg. per sq. cm. pressure, and the moulded materials are preferably dried at 80-100 DEG C. for 12-20 hours in a current of air. To obtain mixed effects, the products may be jointly moulded with phenol-formaldehyde condensation products for which the stated conditions of moulding are suitable. Examples are given describing the manufacture of transparent and opaque products under the conditions set out above, the necessary acidity being obtained by means of oxalic acid or aluminium sulphate, and the fibrous material being cellulose. Other specified fibrous materials are asbestos, cotton, and artificial silk. Filling materials and organic or inorganic colouring materials may also be included, with or without small quantities of fats. Specification 294,253, [Class 2 (iii), Dyes &c.], is referred to.ALSO:Moulding compositions comprise fibrous materials and a mixed condensation product of urea and thiourea with formaldehyde, the condensation product being prepared by condensing a sum of 2 mols. of urea and thiourea jointly with less than 4 mols. of formaldehyde in a medium having a hydrion concentration greater than pH5, preferably pH3, and heating the reactio mixture until a hydrophobe product is obtained. The products form stable sols in the heat, thereby facilitating their incorporation with the fibrous materials; the latter may, however, be present ab initio. The hot solutions, after mixing with the fibrous materials, are dried, first in the air and then by heat, e.g. at 90-100 DEG C. Drying may be effected on heated rolls or in a rotary drum, and at atmospheric or reduced pressure. The products may then be ground and finally heated until a sample loses about 5 per cent of its weight when heated at 100 DEG C. They are then ready for moulding, the small amount of residual water being necessary to ensure sufficient fluidity. Moulding is effected at 140-180 DEG C. at 150-300 kg. per sq. cm. pressure, and the moulded materials are preferably dried at 80-100 DEG C. for 12-20 hours in a current of air. To obtain mixed effects, the products may be jointly moulded with phenol-formaldehyde condensation products for which the stated conditions of moulding are suitable. Specified fibrous materials are cellulose, asbestos, cotton, and artificial silk. Filling materials and organic or inorganic colouring materials may also be included, with or without small quantities of fats. Specification 294,253, [Class 2 (iii), Dyes &c.], is referred to.
GB31010/29A 1928-10-17 1929-10-12 Moulding compositions and moulded articles made therefrom Expired GB344872A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
AT344872X 1928-10-17

Publications (1)

Publication Number Publication Date
GB344872A true GB344872A (en) 1931-03-12

Family

ID=3672251

Family Applications (1)

Application Number Title Priority Date Filing Date
GB31010/29A Expired GB344872A (en) 1928-10-17 1929-10-12 Moulding compositions and moulded articles made therefrom

Country Status (1)

Country Link
GB (1) GB344872A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004065446A1 (en) * 2003-01-24 2004-08-05 Pigmentech Ltd. Condensed urea-formaldehyde compositions and method for production of the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004065446A1 (en) * 2003-01-24 2004-08-05 Pigmentech Ltd. Condensed urea-formaldehyde compositions and method for production of the same

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