Non-aqueous dispersant, color material dispersion liquid for color filter, color filter, liquid crystal display device and organic light-emitting display device
US-2016376443-A1 · Dec 29, 2016 · US
US9540583B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9540583-B2 |
| Application number | US-201313936539-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 8, 2013 |
| Priority date | Jul 9, 2012 |
| Publication date | Jan 10, 2017 |
| Grant date | Jan 10, 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.
Concentrates containing specific functionalized diblock copolymers serve as effective additives for improving the cold flow behavior of fuels and oils, the copolymers being derived from a terminally-unsaturated intermediate polymer obtained via a metallocene process involving hydrogen.
Opening claim text (preview).
What is claimed is: 1. An additive concentrate comprising a functionalised diblock copolymer in admixture with an organic liquid miscible with fuel or oil, the copolymer comprising 2 polymeric blocks wherein: (i) the first block consists of a chain of ethylenic structural units, optionally interrupted by one or more structural units derived from 1-alkene co-monomers higher than ethylene, and (ii) the second block comprises a chain of structural units derived from one or more α,β-unsaturated monomers selected from styrene, substituted styrene, acrylate, methacrylate and diene compounds, and wherein said first and second blocks of the copolymer are terminally joined by the following structural linkage: wherein each R group independently represents an alkyl or aryl group and R′ represents hydrogen or an alkyl group, and wherein the aromatic ring substituent joined to the second block is positioned meta or para to the aromatic ring substituent joined to the first block. 2. The additive concentrate of claim 1 wherein the first and second blocks of the copolymer are terminally joined by the structural linkage: wherein each R group independently represents an alkyl group having from 1 to 4 carbon atoms and R′ represents an alkyl group having from 1 to 10 carbon atoms. 3. The additive concentrate of claim 2 wherein the first and second blocks of the copolymer are terminally joined by the structural linkage: wherein R′ represents an alkyl group having from 1 to 4 carbon atoms. 4. The additive concentrate of claim 3 wherein, in the copolymer, R′ represents n-butyl. 5. The additive concentrate of claim 1 wherein, in the copolymer, the aromatic ring substituent joined to the second block is positioned meta to the aromatic ring substituent joined to the first block. 6. The additive concentrate of claim 1 wherein, in the copolymer, the first block consists of a polyethylene chain. 7. The additive concentrate of claim 1 wherein, in the copolymer, the second block consists of a chain of structural units derived from one or more α,β-unsaturated monomers selected from styrene, substituted styrene, acrylate and methacrylate compounds. 8. The additive concentrate of claim 7 wherein the second block of the copolymer consists of a homo- or copolymeric chain derived from one or more acrylate or methacrylate monomers. 9. The additive concentrate of claim 7 wherein, in the copolymer, the second block consists of homo- or copolymeric chain derived from isoprene or butadiene or both. 10. The additive concentrate of claim 7 wherein the first block of the copolymer has a number average molecular weight (Mn), as measured by GPC against polystyrene standards, in the range of 500 to 20,000. 11. A fuel composition comprising: (i) a base fuel derived from one or more petroleum, animal, vegetable or synthetic sources, the base fuel containing one or more n-alkyl-, iso-alkyl- or n-alkenyl-substituted compounds exhibiting a tendency to crystallise from the base fuel in cold storage or use thereby adversely affecting the cold flow behaviour of the base fuel, and (ii) the additive concentrate of claim 1 , wherein the additive is present in the composition in an amount sufficient to improve the cold flow behaviour of the base fuel during cold storage or use. 12. The composition of claim 11 , wherein the base fuel is a diesel fuel or heating oil. 13. The composition of claim 11 , wherein the base fuel (i) is a base fuel containing one or more n-alkanes containing at least 20 carbon atoms. 14. A method of improving the cold flow behaviour of a fuel composition derived from one or more petroleum, animal, vegetable or synthetic sources and containing one or more n-alkyl-, iso-alkyl- or n-alkenyl-substituted compounds exhibiting a tendency to crystallise from the base fuel in cold storage or use thereby adversely affecting the cold flow behaviour of the base fuel, the method comprising: (i) determining the cold flow behaviour of the base fuel in question and the improvement that is required; (ii) determining the amount of the additive concentrate of claim 1 necessary to effect the desired improvement in cold flow behaviour; and (iii) treating the base fuel with that amount of the additive concentrate. 15. A diblock copolymer comprising: (i) a first block consisting of a chain of ethylenic structural units, optionally interrupted by one or more structural units derived from 1-alkene co-monomers higher than ethylene, and (ii) a second block comprising a chain of structural units derived from one or more α,β-unsaturated monomers selected from styrene, substituted styrene, acrylate, methacrylate and diene compounds, wherein said first and second blocks of the copolymer are terminally joined by means of the following structural linkage: wherein each R group independently represents an alkyl or aryl group and R′ represents hydrogen or an alkyl group, and wherein the aromatic ring substituent joined to the second block is positioned meta or para to the aromatic ring substituent joined to the first block. 16. An oil composition comprising: (i) a base oil derived from one or more petroleum, animal, vegetable or synthetic sources, the base oil containing one or more n-alkyl-, iso-alkyl- or n-alkenyl-substituted compounds exhibiting a tendency to crystallise from the base oil in cold storage or use thereby adversely affecting the cold flow behaviour of the base oil, and (ii) the additive concentrate of claim 1 , wherein the additive is present in the composition in an amount sufficient to improve the cold flow behaviour of the base oil during cold storage or use. 17. The composition of claim 16 , wherein the base oil fuel is a a lubricating oil. 18. The composition of claim 11 , wherein the base oil (i) is a base oil containing one or more n-alkanes containing at least 20 carbon atoms. 19. A method of improving the cold flow behaviour of an oil composition derived from one or more petroleum, animal, vegetable or synthetic sources and containing one or more n-alkyl-, iso-alkyl- or n-alkenyl-substituted compounds exhibiting a tendency to crystallise from the base oil in cold storage or use thereby adversely affecting the cold flow behaviour of the base oil, the method comprising: (i) determining the cold flow behaviour of the base oil in question and the improvement that is required; (ii) determining the amount of the additive concentrate of claim 1 necessary to effect the desired improvement in cold flow behaviour; and (iii) treating the base oil with that amount of the additive concentrate.
Acrylate; Methacrylate · CPC title
containing aromatic monomers, e.g. styrene · CPC title
Monocyclic hydrocarbons · CPC title
modified · CPC title
Cloud point · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.