Organic/inorganic hybrid compound for fouling resistance, membrane including the same for fouling resistance, and method of preparing membrane for fouling resistance
US-9221019-B2 · Dec 29, 2015 · US
US9598523B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9598523-B2 |
| Application number | US-64192109-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 18, 2009 |
| Priority date | Dec 18, 2008 |
| Publication date | Mar 21, 2017 |
| Grant date | Mar 21, 2017 |
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The invention concerns to the use, as an agent improving the thermal stability of (meth)acrylic comb polymers of a macromonomer whose formula (I) is: R-(A-O) m —(B—O) n —R′ (I) wherein both m and n are non-zero and A and B designate alkyl groups having 2 to 4 carbon atoms, but different from one another. The invention further pertains to the implementation of the polymers obtained, as agents improving the thermal stability of the plastic compositions that contain them.
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The invention claimed is: 1. A method for manufacturing a loaded plastic material having improved thermal stability, comprising: preparing by radical copolymerization, a copolymer consisting of units obtained from: a) a (meth)acrylic monomer, and b) a macromonomer having the formula (I): R-(A-O) m —(B—O) n —R′ (I) wherein: m and n are non-zero whole numbers less than 150, A and B refer to alkyl groups having 2 to 4 carbon atoms, wherein alkyl groups A are different from alkyl groups B, and the alkyl groups A and B are distributed in a block or statistical fashion, R designates a polymerizable unsaturated function, and R′ represents hydrogen or an alkyl group having 1 to 40 carbon atoms; wherein the radical copolymerization is a member selected from the group consisting of radical polymerization in a solution, radical polymerization in a direct or reverse emulsion, radical polymerization in a suspension or precipitation in solvents, radical polymerization in the presence of catalytic systems and transfer agents, and controlled radical polymerization; and incorporating the copolymer formed into the loaded plastic material, wherein the plastic material comprises at least one plastic resin selected from the group consisting of thermoplastic resins and heat-setting resins, wherein when the plastic material comprises a thermoplastic resin, the thermoplastic resin is at least one member selected from the group consisting of halogenated resins, styrenic resins, acrylic resins, polyolefins, polycarbonate resins, unsaturated polyester resins, polyurethane resins, polyamide resins, and mixture of these resins, and wherein when the plastic material comprises a heat-setting resin, the heat-setting resin is at least one member selected from the group consisting of acrylic resins, phenoplasts, aminoplasts, and ethoxinlines. 2. The method according to claim 1 , wherein the copolymer is incorporated into the loaded plastic material in an amount of from 0.05% to 5% of said copolymer by dry weight, in comparison to the dry weight of the load. 3. The method according to claim 2 , wherein the copolymer is incorporated in an amount of from 0.1% to 3%. 4. The method according to claim 3 , wherein the copolymer is incorporated in an amount of from 0.1% to 1%. 5. The method according to claim 1 , where the method comprises at least one step of incorporating said copolymer into the loaded plastic material: 1. in the form of a dry powder, resulting from the steps of: grinding and/or dispersing the load in an aqueous medium in the presence of said copolymer, and, optionally, in the presence of at least one other wet-grinding agent and/or at least one other dispersing agent, drying the obtained dispersion and/or aqueous suspension of mineral or carbonated material, optionally adding said polymer, processing and then optionally classifying the obtained powder, 2. and/or in the form of a dry powder, resulting from the steps of: dry-grinding the load in the presence of said copolymer, and optionally in the presence of at least one other dry grinding agent, processing and optionally classifying the obtained powder, 3. and/or in the form of a dry powder, resulting from the following steps: adding said copolymer into a dispersion and/or into an aqueous suspension containing the load, drying the dispersion and/or aqueous suspension of the load, optionally adding said copolymer, processing and then optionally classifying the obtained powder, 4. and/or in the form of a dry powder resulting from drying said copolymer, 5. and/or in the form of a dry powder, resulting from the following steps: adding said copolymer into a suspension and/or emulsion of at least one additive chosen from among at least one member selected from the group consisting of thermal stabilizers, UV stabilizers, lubricants, rheology modifiers, and impact modifiers that are organic in nature, drying the obtained suspension and/or emulsion, optionally in the presence of said copolymer, and then optionally classifying the obtained powder. 6. The method according to claim 1 , wherein the load is a mineral or organic load. 7. The method according to claim 6 , wherein the load is a mineral load selected from the group consisting of natural calcium carbonate, synthetic calcium carbonate, dolomites, limestone, kaolin, talc, titanium dioxide, aluminum trihydroxide, mica, carbon-black, and silica. 8. The method according to claim 7 , wherein the load is natural or synthetic calcium carbonate. 9. The method according to claim 8 , wherein the load is natural calcium carbonate. 10. The method according to claim 1 , wherein the plastic resin is a thermoplastic resin selected from the group consisting of PVC, chlorinated polyvinyl chloride (CPVC), poly(vinylidene fluoride) (PVDF), high-impact styrene-butadiene (HIPS), styrene-acrylonitrile resins, acrylate-butadiene-styrene resins, methyl methacrylate styrene copolymers, methyl polymethacrylate, polyethylenes, polypropylenes, polyethylene terephthalate and polybutylene terephthalate. 11. The method according to claim 10 , wherein the plastic resin is a thermoplastic resin selected from the group consisting of PVC, chlorinated polyvinyl chloride (CPVC), poly(vinylidene fluoride) (PVDF), methyl poly methacrylate, polycarbonate resins, polyethylene terephthalate and polybutylene terephthalate. 12. The method according to claim 11 , wherein the thermoplastic resin is PVC. 13. The method according to claim 1 , wherein the plastic resin is a heat-setting resin selected from the group consisting of acrylic resins, phenoplasts, aminoplasts, and ethoxinlines. 14. The method according to claim 1 , wherein the plastic resin is a heat-setting resin and is a member selected from the group consisting of epoxides, unsaturated polyesters, polyurethanes, and alkyds. 15. The method according to claim 1 , wherein A and B each independently have 2 to 3 carbon atoms. 16. The method according to claim 15 , wherein A is CH 2 —CH 2 and group B is CH 2 —CH(CH 3 )—.
grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds · CPC title
Homopolymers or copolymers obtained by polymerisation of macromolecular compounds terminated by a carbon-to-carbon double bond · CPC title
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Graft or block copolymers according to groups C08L51/00, C08L53/00 or C08L55/02; Derivatives thereof · CPC title
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