Non-hot-melt MDI-based polyurethane composition bearing NCO end groups and having a low content of MDI monomer, comprising at least one isocyanate compound of particular molar volume

US11078322B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11078322-B2
Application numberUS-201916448575-A
CountryUS
Kind codeB2
Filing dateJun 21, 2019
Priority dateMay 28, 2014
Publication dateAug 3, 2021
Grant dateAug 3, 2021

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

1) Polyurethane composition comprising: a) at least 98% by weight of at least one non-hot-melt polyurethane bearing NCO end groups based on diphenyl methane diisocyanates (MDI), b) a MDI monomer content of less than or equal to 1% by weight, c) at least one particular isocyanate compound with a molar volume of less than or equal to 300 millilitres per mole. 2) Process for preparing a polyurethane composition as defined previously, and an adhesive, mastic and/or surface coating composition formulated from such a polyurethane composition.

First claim

Opening claim text (preview).

The invention claimed is: 1. A polyurethane composition comprising: a) at least 98% by weight of at least one non-hot-melt polyurethane bearing NCO end groups based on diphenylmethane diisocyanate (MDI), which polyurethane is not solid at a temperature ranging from 5 to 35° C., and has a MDI content of less than or equal to 1% by weight relative to the weight of the polyurethane composition, b) at least one isocyanate compound with a molar volume of less than or equal to 300 millilitres per mole (mL/mol), noted compound A, in which the isocyanate group or groups are not linked to a carbon atom of an aromatic hydrocarbon-based ring, the weight percentages being expressed relative to the total weight of the polyurethane composition. 2. The composition according claim 1 , wherein the non-hot-melt polyurethane(s) bearing NCO end groups based on MDI may be obtained via a polyaddition reaction of a polyisocyanate composition consisting of MDI, and of a composition consisting of polyol(s), at a temperature of less than 95° C., under anhydrous conditions, in amounts of polyisocyanate(s) and of polyol(s) leading to an NCO/OH ratio noted r1 ranging from 1.60 to 1.95. 3. The composition according to claim 2 , wherein the temperature ranges from 70 to 80° C. and the NCO/OH ratio noted r1 ranges from 1.60 to 1.75. 4. The composition according to claim 2 , wherein the composition consisting of polyol(s) is a mixture of polyether diol and polyether triol. 5. The composition according to claim 1 , comprising: from 10% to 30% by weight of the polyurethane composition, from 25% to 70% by weight of at least one filler, from 0.01% to 1% by weight of at least one crosslinking catalyst, the weight percentages being expressed relative to the total weight of the composition. 6. A composition comprising: a) at least 98% by weight of at least one non-hot-melt polyurethane bearing NCO end groups based on diphenylmethane diisocyanate noted MDI b) a content of MDI monomer of less than or equal to 1% by weight, c) at least one isocyanate compound with a molar volume of less than or equal to 300 millilitres per mole noted compound A, which compound is different from MDI and in which the isocyanate group or groups are not linked to a carbon atom of an aromatic hydrocarbon-based ring, the weight percentages being expressed relative to the total weight of the polyurethane composition. 7. A composition comprising: a) at least 98% by weight of at least one non-hot-melt polyurethane bearing NCO end groups based on diphenylmethane diisocyanate noted MDI b) a content of MDI monomer of less than or equal to 1% by weight, c) at least one isocyanate compound with a molar volume of less than or equal to 300 millilitres per mole noted compound A, in which the isocyanate group or groups are not linked to a carbon atom of an aromatic hydrocarbon-based ring, compound A being an aliphatic, acyclic, linear or branched monoisocyanate, benzyl monoisocyanate, cycloaliphatic monoisocyanate, benzyl diisocyanate, cycloaliphatic diisocyanate, or a linear or branched acyclic aliphatic diisocyanate, the weight percentages being expressed relative to the total weight of the polyurethane composition, said process. 8. The composition according to claim 1 , wherein compound A is XDI, IPDI, HMDI or a mixture thereof.

Assignees

Inventors

Classifications

  • containing oxypropylene or higher oxyalkylene end groups · CPC title

  • containing two or more cycloaliphatic rings · CPC title

  • containing only one alkylene bisphenyl group · CPC title

  • Carbonates; Bicarbonates · CPC title

  • Compositions for pressure-sensitive adhesives · CPC title

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Frequently asked questions

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What does patent US11078322B2 cover?
1) Polyurethane composition comprising: a) at least 98% by weight of at least one non-hot-melt polyurethane bearing NCO end groups based on diphenyl methane diisocyanates (MDI), b) a MDI monomer content of less than or equal to 1% by weight, c) at least one particular isocyanate compound with a molar volume of less than or equal to 300 millilitres per mole. 2) Process for prepari…
Who is the assignee on this patent?
Bostik Sa
What technology area does this patent fall under?
Primary CPC classification C08G18/4845. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Aug 03 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).