GB878542A - Caulking compositions - Google Patents

Caulking compositions

Info

Publication number
GB878542A
GB878542A GB35386/59A GB3538659A GB878542A GB 878542 A GB878542 A GB 878542A GB 35386/59 A GB35386/59 A GB 35386/59A GB 3538659 A GB3538659 A GB 3538659A GB 878542 A GB878542 A GB 878542A
Authority
GB
United Kingdom
Prior art keywords
phthalate
benzyl
caulks
equivalents
polyol
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
GB35386/59A
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 GB878542A publication Critical patent/GB878542A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/34Filling pastes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B63SHIPS OR OTHER WATERBORNE VESSELS; RELATED EQUIPMENT
    • B63BSHIPS OR OTHER WATERBORNE VESSELS; EQUIPMENT FOR SHIPPING 
    • B63B5/00Hulls characterised by their construction of non-metallic material
    • B63B5/02Hulls characterised by their construction of non-metallic material made predominantly of wood
    • B63B5/06Decks; Shells
    • B63B5/065Decks; Shells caulking decks
    • 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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/2805Compounds having only one group containing active hydrogen
    • 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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67Unsaturated compounds having active hydrogen
    • C08G18/671Unsaturated compounds having only one group containing active hydrogen
    • C08G18/6715Unsaturated monofunctional alcohols or amines
    • 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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/71Monoisocyanates or monoisothiocyanates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04Polyurethanes
    • 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
    • C08G2190/00Compositions for sealing or packing joints

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Combustion & Propulsion (AREA)
  • Mechanical Engineering (AREA)
  • Ocean & Marine Engineering (AREA)
  • Materials Engineering (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Sealing Material Composition (AREA)

Abstract

A stable, low-modulus caulk comprises as an essential constituent the polyurethane reaction product of (1) at least one polymeric polyol which is a polyalkylene-ether glycol or polyester, the polyol having an average molecular weight of 400-3,000, an acid number of less than 5 and an average of 2-3 free hydroxyl groups per molecule; (2) from 1,2-2,0 equivalents of at least one organic diisocyanate for each equivalent of polyol, and (3) from 0,003-0,0835 equivalents of monofunctional modifier selected from saturated primary alcohols, saturated primary amines and monofunctional saturated isocyanates for each equivalent of organic diisocyanate. In the figure for equivalents the last digit given is a significant figure in the mathematical sense. Substituted and unsubstituted polyalkylene ether glycols, linear polyesters, alkyd resins and aromatic, aliphatic and cycloaliphatic diisocyanates are listed. As the third component used in preparing the polyurethane there are specified methanol, ethanol, propanol, 2-methyl-propanol-1, butanol, hexanol, octanol, 2-ethylhexanol, decanal, octadecanal, benzyl alcohol, 2-cyclohexylethanol, 2-methoxy-ethanol, 4-acetoxybutanol; methylamine, ethylamine, propylamine, 2-methylbutylamine, n-hexylamine, octylamine, octadecylamine, 2-cyclohexylethylamine and benzylamine; phenyl, 4-tolyl, naphthyl, 4-chlorophenyl, butyl, hexyl, decyl, octadecyl, cyclohexyl, and tetrahydronaphthyl isocyanates. Nonslumping caulks are obtained by incorporating a finely divided particulate or fibrous antislumping agent, the particles preferably having a size of 0,01-0,04 microns and a surface area of 100-400 square metres per gram and the fibres preferably having a fibre length of 1/16 inch or less. Specified are titanium dioxide, silica, carbon black, zinc oxide, glass, aluminium oxide, talc; fibres of glass, polyacrylonitrile, polyamides, polyethylene, polyethylene terephthalate, wood flour, leather dust and asbestos. There may also be added fillers such as iron oxide, calcium carbonate, talc, magnesium oxide, diatomaceous earth, metal oxides, chromates, silicates, sulphides, sulphates and carbonates; plasticizers such as di (2-ethylhexyl) phthalate, or azelate, benzyl butyl phthalate, dibutyl phthalate, triphenyl phosphate, 2-ethylhexyl benzyl phthalate, low molecular weight polyurethanes, dicyclohexyl phthalate, triacetylated castor oil and epoxidized soy bean oil; antioxidants such as di-(p-tertiary butyl) cresol, 2-benzyl-6-tertiary butyl p-cresol, polymerized trimethyl dihydroquinoline, phenyl a - or b -naphthyl-amine, hydroquinone monobutyl ether and paraffin hydrocarbons. The caulks can be prepared by heating the polyalkylene-ether glycol or polyester with a solvent such as hexane, decane, xylene, benzene, toluene or naphtha with azeotropic distillation of water. Next the mixture is heated at 80 DEG -120 DEG C. with the organic diisocyanate, and after some hours the monofunctional reactant is added and heating is continued. After application the caulks cure under normal atmospheric conditions. Curing can be accelerated by subjecting to a more humid atmosphere or by adding to the composition a tertiary amine such as butylamine, trimethylamine, dimethyl dodecylamine or N-methyl morpholine.
GB35386/59A 1958-10-28 1959-10-19 Caulking compositions Expired GB878542A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US878542XA 1958-10-28 1958-10-28

Publications (1)

Publication Number Publication Date
GB878542A true GB878542A (en) 1961-10-04

Family

ID=22207642

Family Applications (1)

Application Number Title Priority Date Filing Date
GB35386/59A Expired GB878542A (en) 1958-10-28 1959-10-19 Caulking compositions

Country Status (3)

Country Link
FR (1) FR1237936A (en)
GB (1) GB878542A (en)
NL (1) NL244519A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1983002453A1 (en) * 1982-01-20 1983-07-21 Grouiller, Hervé New utilization of a thermoplastic material as a sealing means, particularly for fixing an insert
GB2137638A (en) * 1983-04-05 1984-10-10 Bostik Ltd Adhesive compositions
US4888124A (en) * 1985-05-14 1989-12-19 Basf Aktiengesellschaft Preparation of stable dispersions of finely divided polyisocyanates and preparation of heat-crosslinkable isocyanate systems

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2126932A1 (en) * 1971-01-28 1972-10-13 Naphtachimie Sa Polyurethane coatings - for use in making artificial leathers
DE3228723A1 (en) * 1982-07-31 1984-02-02 Basf Farben + Fasern Ag, 2000 Hamburg STORAGE-STABLE, HEAT-CURABLE MATERIAL MIXTURES MADE OF POLYISOCYANATE AND COMPOUNDS WITH REACTIVE COMPOSITIONS, METHOD FOR THE PRODUCTION AND USE THEREOF
EP0100507B1 (en) * 1982-07-31 1988-10-26 BASF Lacke + Farben AG Thermosetting mixtures of polyisocyanates and polyoles having an extended storage life, process for their preparation, and their use
US4642321A (en) * 1985-07-19 1987-02-10 Kollmorgen Technologies Corporation Heat activatable adhesive for wire scribed circuits
US5340946A (en) * 1985-12-20 1994-08-23 Advanced Interconnection Technology, Inc. Heat activatable adhesive for wire scribed circuits

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1983002453A1 (en) * 1982-01-20 1983-07-21 Grouiller, Hervé New utilization of a thermoplastic material as a sealing means, particularly for fixing an insert
FR2520069A1 (en) * 1982-01-20 1983-07-22 Lhd Lab Hygiene Dietetique NEW USE OF A THERMOPLASTIC MATERIAL AS A SEALING MEDIUM, ESPECIALLY FOR FIXING THE INSERT
GB2137638A (en) * 1983-04-05 1984-10-10 Bostik Ltd Adhesive compositions
US4888124A (en) * 1985-05-14 1989-12-19 Basf Aktiengesellschaft Preparation of stable dispersions of finely divided polyisocyanates and preparation of heat-crosslinkable isocyanate systems

Also Published As

Publication number Publication date
NL244519A (en)
FR1237936A (en) 1960-08-05

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