Storage-Stable 1K Spray Adhesives Based on Polyurethane Dispersions
US-2024101879-A1 · Mar 28, 2024 · US
US2016333236A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016333236-A1 |
| Application number | US-201615202614-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 6, 2016 |
| Priority date | Jan 14, 2014 |
| Publication date | Nov 17, 2016 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present specification relates to moisture reactive hot melt adhesive compositions comprising a silane reactive plasticizer and the reaction product of (i) a semi-crystalline polyol and (ii) a polyisocyanate and (iii) an aminosilane; the production of such adhesives; and the use of such adhesives.
Opening claim text (preview).
1 . A moisture curable composition comprising: a reaction product of (i) a semi-crystalline polyol and (ii) a polyisocyanate and (iii) a primary aminosilane; and a silane reactive plasticizer. 2 . The moisture curable composition of claim 1 wherein the equivalent ratio of polyisocyanate (ii) to semi-crystalline polyol (i) is >1.4. 3 . The moisture curable composition of claim 1 wherein the ratio of equivalents of primary aminosilane (iii) to [equivalents of polyisocyanate (ii)−equivalents of semi-crystalline polyol (i)] is about 1 or greater. 4 . The moisture curable composition of claim 1 being free of water and solvent. 5 . The moisture curable composition of claim 1 wherein the equivalent ratio of polyisocyanate (ii) to semi-crystalline polyol (i) is >1. 6 . The moisture curable composition of claim 1 further comprising adhesion promoter. 7 . The moisture curable composition of claim 1 further comprising an aminosilane adhesion promoter. 8 . The moisture curable composition of claim 1 wherein the equivalent ratio of isocyanate to polyol is greater than 1 to 1. 9 . The moisture curable composition of claim 1 wherein the equivalent ratio of isocyanate to polyol is greater than 1.6 to 1. 10 . The moisture curable composition of claim 1 further comprising one or more of a tackifier; an acrylic polymer; and a catalyst. 11 . The moisture curable composition of claim 1 wherein weight ratio of polyester polyol to silane reactive plasticizer is greater than 1 part polyester polyol to 1 part silane reactive plasticizer. 12 . The moisture curable composition of claim 1 wherein weight ratio of polyester polyol to silane reactive plasticizer is greater than 1.2 parts polyester polyol to 1 part silane reactive plasticizer. 13 . The moisture curable composition of claim 1 wherein the silane reactive plasticizer comprises at least one silyl group with a formula of R-[A-Si(C x H 2x+1 ) n (OH) 3−n ] z or R-[A-Si(C x H 2x+1 ) n (OC y H 2y+1 ) 3−n ] z wherein R is a polymer backbone; A is a linkage to the polymer backbone; x is 1 to 12; y is 1 to 12; and n is 0, 1 or 2. 14 . The moisture curable composition of claim 13 , wherein polymer backbone R is selected from silicone, polyether, polycarbonate, polyisobutylene, ethylene vinyl acetate and polyacrylate. 13 . (canceled) 14 . (canceled) 15 . The moisture curable composition of claim 1 being free of isocyanate monomer. 16 . The moisture curable composition of claim 1 comprising about 70 to about 90 weight percent reaction product and about 10 to about 30 weight percent silane reactive plasticizer. 17 . A method of applying a moisture curable composition comprising: providing the moisture curable composition of claim 1 in solid form at room temperature; heating the moisture curable composition to a molten state at the point of use; applying the molten moisture curable composition to a first substrate; bringing a second substrate in contact with the molten moisture curable composition applied to the first substrate; cooling the applied molten moisture curable composition to a solid state; subjecting the cooled composition to conditions sufficient to irreversibly cure the cooled composition to form a bond between the first and second substrates. 18 . An article of manufacture comprising the moisture curable composition of claim 1 . 19 . A moisture curable hot melt adhesive comprising the moisture curable composition of claim 1 . 20 . The moisture curable composition of claim 1 in cured form. 21 . The moisture curable composition of claim 1 , wherein the silane reactive plasticizer is a liquid at room temperature and polymer backbone R is selected from polyether, polycarbonate, polyisobutylene, and polyacrylate. 22 . The moisture curable composition of claim 1 wherein the reaction product comprises a plurality of terminal silyl groups each independently having a formula of: R-[A-Si(C x H 2x+1 ) n (OC y H 2y+1 ) 3−n ] z wherein R is the polyester backbone; A is a linkage that links the silane to polymer backbone R; n=0, 1 or 2; x and y are, independently a number from 1 to 12.
containing hydrolysable silane groups · CPC title
from polyesters · CPC title
from polyesters · CPC title
containing silicon bound to organic groups containing atoms other than carbon, hydrogen, and oxygen · CPC title
Unsaturated polyesters · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.