Resin composition and battery module comprising the same
US-11909053-B2 · Feb 20, 2024 · US
US9701780B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9701780-B2 |
| Application number | US-201615052343-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 24, 2016 |
| Priority date | May 30, 2012 |
| Publication date | Jul 11, 2017 |
| Grant date | Jul 11, 2017 |
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.
A polybutadiene having a hydroxyl group at a terminal end thereof is reacted with a lactone compound such as an ε-caprolactone to obtain a polymer polyol represented by formula (I): HO—X 1 —Y—X 2 —OH (wherein X 1 and X 2 each independently represents a polyester component and Y represents a polybutadiene component), the polymer polyol is reacted with an unsymmetric diisocyanate to obtain a urethane prepolymer, and then the urethane prepolymer is reacted with a chain extender to obtain a polyurethane.
Opening claim text (preview).
The invention claimed is: 1. A method for preparing a polyurethane, comprising: reacting a polybutadiene having a hydroxyl group at a terminal end thereof with an ε-caprolactone to obtain a polymer polyol of formula (I); reacting the polymer polyol and an unsymmetric diisocyanate to obtain a urethane prepolymer having an isocyanate group at a terminal end thereof, wherein an amount of the unsymmetric diisocyanate is determined so that a molar ratio of a mole number of isocyanate groups derived from the unsymmetric diisocyanate to a mole number of hydroxyl groups derived from the polymer polyol is within a range of 2.1 to 3.8; and then reacting a chain extender with the urethane prepolymer to obtain the polyurethane, wherein an amount of the chain extender is determined so that a molar ratio of the mole number of the isocyanate groups derived from the unsymmetric diisocyanate with reference to a total mole number of hvdroxyl groups derived from the polymer polyol and the chain extender is within a range of 0.9 to 1.1, HO—X 1 —Y—X 2 —OH (I) wherein: X 1 and X 2 each independently represents a polyester component, and Y represents a polybutadiene component consisting of: a 1,4-structure consisting of a repeating unit represented by formula (IVb); and a 1,2-structure consisting of a repeating unit represented by formula (Vb): wherein a molar ratio of the 1,2-structure/the 1,4-structure is within a range from 90.4/9.6 to 95/5. 2. The method according to claim 1 , wherein the chain extender is an aliphatic glycol.
Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step · CPC title
containing carboxylic ester groups · CPC title
Valcrolactone and/or substituted valcrolactone · CPC title
Polymers of conjugated dienes {(hydrogenated polymers of conjugated dienes C08G18/6208)} · CPC title
aliphatic · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.