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US4193832A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for making bonds

Assignee: Bayer AG
•
Filing: 1978-04-24
•
Granted: 1980-03-18
•
Expires: 1998-04-24
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Abstract

Abstract The instant invention is directed to a method for bonding one or more substrates by applying adhesives comprising organic polyisocyanates and compounds containing isocyanate-reactive hydrogen atoms which react to form polyurethanes, or moisture-hardening reaction products containing free isocyanate groups or excess quantities of polyisocyanates and compounds containing isocyanate-reactive hydrogen atoms, the improvement wherein said compounds containing isocyanate-reactive hydrogen atoms are dispersions of polymers in organic polyhydroxyl compounds.

Inventors

  • 👤 Artur Reischl
  • 👤 Rudolf Hombach
  • 👤 Manfred Dollhausen

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-27 10:15
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/08; C08G18/0838; C08G18/0842; C08G18/0861; C08G18/0871; C08G18/0876; C09; C09J; C09J175/00; C09J175/04; C08L; C08L2666/00; C08L2666/02; Y; Y10; Y10T; Y10T428/00; Y10T428/31504; Y10T428/31551

Claims Analysis

Total Claims: 15
Claim 1
Independent Claim 142 words
In a method for bonding one or more substrates with polyurethane adhesives comprising: (A) applying to at least one of the surfaces to be bonded adhesives comprising organic polyisocyanates and compounds containing isocyanate-reactive hydrogen atoms which react with each other to form polyurethanes, or moisture-hardening reaction products containing free isocyanate groups or excess quantities of polyisocyanates and compounds containing isocyanate-reactive hydrogen atoms which react with each other and (B) fitting together said surfaces to be bonded, the improvement wherein said compounds containing isocyanate-reactive hydrogen atoms are dispersions of isocyanate polyaddition products which contain terminal hydroxyl groups and primary or secondary amino groups or semicarbazide groups, in organic polyhydroxyl compounds, prepared from diisocyanates having a molecular weight of from 112 to 300 and compounds containing isocyanate-reactive groups having a functionality of at least two and a molecular weight of from 32 to 300.
Claim 2
Dependent Claim 142 words
In a method for bonding one or more substrates with polyurethane adhesives comprising: (A) applying to at least one of the surfaces to be bonded adhesives comprising organic polyisocyanates and compounds containing isocyanate-reactive hydrogen atoms which react with each other to form polyurethanes, or moisture-hardening reaction products containing free isocyanate groups or excess quantities of polyisocyanates and compounds containing isocyanate-reactive hydrogen atoms which react with each other and (B) fitting together said surfaces to be bonded, the improvement wherein said compounds containing isocyanate-reactive hydrogen atoms are dispersions of isocyanate polyaddition products which contain terminal hydroxyl groups and primary or secondary amino groups or semicarbazide groups, in organic polyhydroxyl compounds, prepared from diisocyanates having a molecular weight of from 112 to 300 and compounds containing isocyanate-reactive groups having a functionality of at least two and a molecular weight of from 32 to 300.
Claim 3
Dependent Claim 35 words
The method of claim 1, wherein said diisocyanates of said low molecular weight units are selected from the group consisting of 2,4-diisocyanatotoluene, 2,6-diisocyanatotoluene, ethylene diisocyanate, hexamethylene diisocyanate, 3,3,5-trimethyl-5-isocyanatomethyl cyclohexyl isocyanate, 4,4'-diisocyanatodiphenyl methane, and mixtures thereof.
Claim 4
Dependent Claim 45 words
The method of claim 1, wherein said isocyanate-reactive groups of said low molecular weight units are selected from the group consisting of hydrazine, ethylene diamine, hexamethylene diamine, 2,4-diaminotoluene, 2,6-diaminotoluene, 4,4'-diaminodiphenyl methane, aminoethanol, 2-aminopropanol, N,N-diethanolamine, ethylene glycol, trimethylene glycol, 1,2-propane diol, hexamethylene glycol, and mixtures thereof.
Claim 5
Dependent Claim 18 words
The method of claim 1, wherein said organic polyhydroxyl compounds have a molecular weight from 200 to 4,000.
Claim 6
Dependent Claim 18 words
The method of claim 4, wherein said organic polyhydroxyl compounds have a molecular weight from 400 to 2,500.
Claim 7
Dependent Claim 39 words
The method of claim 1, wherein said organic polyhydroxyl compounds are mixtures of different polyhydroxyl compounds having an average molecular weight of from 200 to 4,000 and the individual organic polyhydroxyl compounds have molecular weights from 62 to 20,000.
Claim 8
Dependent Claim 21 words
The method of claim 6, wherein said mixtures of different polyhydroxyl compounds have an average molecular weight of 400 to 2,500.
Claim 9
Dependent Claim 27 words
The method of claim 1, wherein said organic polyhydroxyl groups are selected from the group consisting of polyhydric alcohols, polyether polyols, and natural oils containing hydroxyl groups.
Claim 10
Dependent Claim 26 words
The method of claim 1, wherein said dispersions have a solids content of from 3 to 60%, by weight, based on the dispersion as a whole.
Claim 11
Dependent Claim 13 words
The method of claim 9, wherein said solids content is 10 to 50%.
Claim 12
Dependent Claim 27 words
The method of claim 1, wherein said dispersions are sedimentation-stable and are in the form of 20% solutions having a viscosity at 25° C. below 100,000 cP.
Claim 13
Dependent Claim 18 words
The method of claim 11, wherein the dispersed particles have a size of from 0.01 to 10 μm.
Claim 14
Dependent Claim 21 words
The method of claim 1, wherein said organic polyisocyanates are selected from the group consisting of 2,4-diisocyanatotoluene, 2,6-diisocyanatotoluene, and mixtures thereof.
Claim 15
Dependent Claim 23 words
The method of claim 1, wherein said organic polyisocyanates are selected from the group consisting of 2,4'-diisocyanatodiphenyl methane, 4,4'-diisocyanatodiphenyl methane, and mixtures thereof.

References Cited (Backward Citations)

US3218215A Cited
US3523093A Cited
US3522218A Cited
US3770555A Cited
GB1408510A Cited
US4089835A Cited
US4092275A Cited
US4093569A Cited
US4147680A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-03-18 1983-09-17 1984-03-18 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-03-18 1987-09-17 1988-03-18 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-03-18 1991-09-17 1992-03-18 $7700.00 Window Closed / Lapsed

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