Binder composition for non-aqueous secondary battery electrode

US2016156039A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016156039-A1
Application numberUS-201615013127-A
CountryUS
Kind codeA1
Filing dateFeb 2, 2016
Priority dateApr 3, 2009
Publication dateJun 2, 2016
Grant date

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  1. Title

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  2. Abstract

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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.

A binder composition for a non-aqueous secondary battery electrode may comprise functional group-containing crosslinked resin microparticles produced by polymerizing: (A) at least one monomer selected from the group consisting of (a) a monomer having one ethylenically unsaturated group per molecule and also having a monofunctional or polyfunctional epoxy group, (b) a monomer having one ethylenically unsaturated group per molecule and also having a monofunctional or polyfunctional amide group, and (c) a monomer having one ethylenically unsaturated group per molecule and also having a monofunctional or polyfunctional hydroxy group; (B) at least one monomer selected from the group consisting of (d) a monomer having one ethylenically unsaturated group per molecule and also having an alkoxysilyl group and (e) a monomer having at least two ethylenically unsaturated groups per molecule; and (C) (k) a monomer which has an ethylenically unsaturated group and is different from the monomers (a) to (e).

First claim

Opening claim text (preview).

1 . A non-aqueous secondary battery electrode comprising a binder composition that contains fine particles of a functional group-containing cross-linking resin, wherein the fine particles of a functional group-containing cross-linking resin are fine particles of the resin obtained by emulsification polymerization of monomers having an ethylenically unsaturated group with a radical polymerization initiator in water in the presence of a surfactant, wherein the monomers having an ethylenically unsaturated group contains: (A) 0.1 to 20% by weight of at least one monomer that is selected from the group consisting of (a) a monomer having one ethylenically unsaturated group per molecule and also having one or more epoxy groups, (b) a monomer having one ethylenically unsaturated group per molecule and also having one or more-amide groups, and (c) a monomer having one ethylenically unsaturated group per molecule and also having one or more hydroxide groups; (B) 0.1 to 5% by weight of at least one monomer that is selected from the group consisting of (d) a monomer having one ethylenically unsaturated group per molecule and also having one or more alkoxysilyl groups, and (e) a monomer having two or more ethylenically unsaturated groups per molecule; and (C) 75 to 99.8% by weight of (k) a monomer which has an ethylenically unsaturated group and is different from the monomers (a) to (e), having an ethylenically unsaturated group contains at least (m) a monomer having one ethylenically unsaturated group per molecule and also having a C 8-18 alkyl group and/or (n) a monomer having one ethylenically unsaturated group per molecule and also having a cyclic structure, wherein the monomers (m) and (n) are included in 30 to 95% by weight in sum in total monomers having an ethylenically unsaturated group ((a) to (e) and (k)), wherein the monomer (a) is selected from at least one of glycidyl(meth)acrylate and 3,4-epoxy cyclohexyl(meth)acrylate; the monomer (b) is selected from at least one of (meth)acrylic amide, diacetone(meth)acrylate amide, N-methylol acrylic amide, N,N-di(methylol)acrylic amide and N-methylol-N-methoxymethyl(meth)acrylic amide; the monomer (c) is selected from at least one of 2-hydroxyethyl(meth)acrylate, 2-hydroxypropyl(meth)acrylate and 4-hydroxybutyl(meth)acrylate; the monomer (d) is selected from at least one of γ-methacryloxypropyltrimethoxysilane, γ-methacryloxypropyltriethoxysilane, γ-methacryloxypropyltributoxysilane, γ-methacryloxypropylmethyldimethoxysilane, γ-methacryloxypropylmethyldiethoxysilane, γ-acryloxypropyltrimethoxysilane, γ-acryloxypropyltriethoxysilane, γ-acryloxypropylmethyldimethoxysilane, γ-methacryloxymethyltrimethoxysilane, γ-acryloxymethyltrimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, vinyltributoxysilane, and vinylmethyldimethoxysilane; the monomer (e) contains allyl(meth)acrylate; the monomer (m) is selected from at least one of 2-ethylhexyl(meth)acrylate, lauryl(meth)acrylate, myristyl(meth)acrylate, cetyl(meth)acrylate and stearyl(meth)acrylate; and the monomer (n) is selected from at least one of styrene, α-methyl styrene, 2-methyl styrene, cyclohexyl(meth)acrylate, isobonyl(meth)acrylate, benzyl(meth)acrylate and phenoxyethyl(meth)acrylate. 2 . The non-aqueous secondary battery electrode of claim 1 , wherein the composition further comprises (D) anon-cross-linked compound that is selected from the group consisting of a non-cross-linked epoxy group-containing compound, a non-cross-linked amide group-containing compound, a non-cross-linked hydroxide group-containing compound, and a non-cross-linked oxazoline group-containing compound. 3 . The non-aqueous secondary battery electrode of claim 1 , wherein the monomers (A) constitute 1 to 15% by weight of the composition. 4 . The non-aqueous secondary battery electrode of claim 1 , wherein the monomers (A) constitute 2 to 10% by weight of the composition. 5 . The non-aqueous secondary battery electrode of claim 1 , wherein the monomers (B) constitute 0.5 to 3% by weight of the composition. 6 . The non-aqueous secondary battery electrode of claim 1 , wherein the monomers having an ethylenically unsaturated group further comprise at least one keto group-containing ethylenically unsaturated monomer, which constitutes 0.1 to 10% by weight with respect to the total monomers having an ethylenically unsaturated group ((a) to (e) and (k)) in the composition. 7 . The non-aqueous secondary battery electrode of claim 6 , wherein the at least one keto group-containing ethylenically unsaturated monomer constitutes 1 to 8% by weight with respect to the total monomers having an ethylenically unsaturated group ((a) to (e) and (k)) in the composition. 8 . The non-aqueous secondary battery electrode of claim 6 , wherein the at least one keto group-containing ethylenically unsaturated monomer constitutes 3 to 7% by weight with respect to the total monomers having an ethylenically unsaturated group ((a) to (e) and (k)) in the composition. 9 . The non-aqueous secondary battery electrode of claim 6 , wherein the at least one keto group-containing ethylenically unsaturated monomer comprises diacetone(meth)acrylic amide. 10 . The non-aqueous secondary battery electrode of claim 1 comprising: i) an electrode-active material; ii) a conductive auxiliary agent; iii) a binder comprising the binder composition; and iv) a current collector, wherein the binder attaches the electrode-active material and the conductive auxiliary agent to the current collector. 11 . A non-aqueous secondary battery comprising: a non-aqueous secondary battery electrode comprising a binder composition that contains fine particles of a functional group-containing cross-linking resin, wherein the fine particles of a functional group-containing cross-linking resin are fine particles of the resin obtained by emulsification polymerization of monomers having an ethylenically unsaturated group with a radical polymerization initiator in water in the presence of a surfactant, wherein the monomers having an ethylenically unsaturated group contains: (A) 0.1 to 20% by weight of at least one monomer that is selected from the group consisting of (a) a monomer having one ethylenically unsaturated group per molecule and also having one or more epoxy groups, (b) a monomer having one ethylenically unsaturated group per molecule and also having one or more amide groups group, and (c) a monomer having one ethylenically unsaturated group per molecule and also having one or more hydroxide groups; (B) 0.1 to 5% by weight of at least one monomer that is selected from the group consisting of (d) a monomer having one ethylenically unsaturated group per molecule and also having one or more alkoxysilyl groups, and (e) a monomer having two or more ethylenically unsaturated groups per molecule; and (C) 75 to 99.8% by weight of (k) a monomer which has an ethylenically unsaturated group and is different from the monomers (a) to (e), having an ethylenically unsaturated group contains at least (m) a monomer having one ethylenically unsaturated group per molecule and also having a C 8-18 alkyl group and/or (n) a monomer having one ethylenically unsaturated group per molecule and also having a cyclic structure, wherein the monomers (m) and (n) are included in 30 to 95% by weight in sum in total monomers having an ethylenically unsaturated group ((a) to (e) and (k)), wherein the monomer (a) is selected from at least one of glycidyl(meth)acrylate and 3,4-epoxy cyclohexyl(meth)acrylate; the monomer (b) is selected from at least one of (meth)acrylic amide, diacetone(meth)acrylate amide, N-methylol acrylic amide, N,N-di(methylol) acrylic amide and N-methylol-N-methoxymethyl(meth)acry

Assignees

Inventors

Classifications

  • Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title

  • H01M4/622Primary

    being polymers · CPC title

  • Batteries in portable systems, e.g. mobile phone, laptop · CPC title

  • Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof · CPC title

  • Energy storage using capacitors · CPC title

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What does patent US2016156039A1 cover?
A binder composition for a non-aqueous secondary battery electrode may comprise functional group-containing crosslinked resin microparticles produced by polymerizing: (A) at least one monomer selected from the group consisting of (a) a monomer having one ethylenically unsaturated group per molecule and also having a monofunctional or polyfunctional epoxy group, (b) a monomer having one ethyleni…
Who is the assignee on this patent?
Toyo Ink Sc Holdings Co Ltd, Toyocolor Co Ltd
What technology area does this patent fall under?
Primary CPC classification H01M4/622. Mapped technology areas include Electricity.
When was this patent published?
Publication date Thu Jun 02 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).