An electrode binder of a lithium ion secondary battery comprising an aqueous dispersion of: (a) a polyvinylidene binder; (b) a (meth)acrylic polymer dispersant; (c) a crosslinking agent comprising an aminoplast and/or a polycarbodiimide; and (d) an organic diluent. The (meth)acrylic polymer dispersant is prepared from a mixture of monomers comprising one or more carboxylic acid group-containing (meth)acrylic monomers and one or more hydroxyl group-containing (meth)acrylic monomers, and carboxylic acid groups on the (meth)acrylic polymer dispersant are at least partially neutralized with a base. The binder can be used in the assembly of electrodes of lithium ion secondary batteries.

An electrode binder of a lithium ion secondary battery comprising an aqueous dispersion of: (a) a polyvinylidene binder; (b) a (meth)acrylic polymer dispersant; (c) a crosslinking agent comprising an aminoplast and/or a polycarbodiimide; and (d) an organic diluent. The (meth)acrylic polymer dispersant is prepared from a mixture of monomers comprising one or more carboxylic acid group-containing (meth)acrylic monomers and one or more hydroxyl group-containing (meth)acrylic monomers, and carboxylic acid groups on the (meth)acrylic polymer dispersant are at least partially neutralized with a base. The binder can be used in the assembly of electrodes of lithium ion secondary batteries.

An electrode binder of a lithium ion secondary battery comprising an aqueous dispersion of: (a) a polyvinylidene binder; (b) a (meth)acrylic polymer dispersant; (c) a crosslinking agent comprising an aminoplast and/or a polycarbodiimide; and (d) an organic diluent. The (meth)acrylic polymer dispersant is prepared from a mixture of monomers comprising one or more carboxylic acid group-containing (meth)acrylic monomers and one or more hydroxyl group-containing (meth)acrylic monomers, and carboxylic acid groups on the (meth)acrylic polymer dispersant are at least partially neutralized with a base. The binder can be used in the assembly of electrodes of lithium ion secondary batteries.

A method of making a flexible pipe layer, which method comprises: commingling polymer filaments and carbon fibre filaments to form an intimate mixture, forming yarns of the commingled filaments, forming the yarns into a tape, and applying the tape to a pipe body to form a flexible pipe layer.

A method of making a flexible pipe layer, which method comprises: commingling polymer filaments and carbon fibre filaments to form an intimate mixture, forming yarns of the commingled filaments, forming the yarns into a tape, and applying the tape to a pipe body to form a flexible pipe layer.

High spherical particles for use in piezoelectric applications may be produced mixing a mixture comprising a graphene oxide-polyvinylidene fluoride (GO-PVDF) composite, a carrier fluid that is immiscible with the PVDF, and optionally an emulsion stabilizer at a temperature equal to or greater than a melting point or softening temperature of the PVDF to disperse the GO-PVDF composite in the carrier fluid, wherein the GO-PVDF composite has a transmission FTIR minimum transmittance ratio of β-phase PVDF to α-phase PVDF of about 1 or less; cooling the mixture to below the melting point or softening temperature of the PVDF to form GO-PVDF particles; and separating the GO-PVDF particles from the carrier fluid, wherein the GO-PVDF particles comprise the graphene oxide dispersed in the PVDF, and wherein the GO-PVDF particles have a transmission FTIR minimum transmittance ratio of β-phase PVDF to α-phase PVDF of about 1 or less.

High spherical particles for use in piezoelectric applications may be produced mixing a mixture comprising a graphene oxide-polyvinylidene fluoride (GO-PVDF) composite, a carrier fluid that is immiscible with the PVDF, and optionally an emulsion stabilizer at a temperature equal to or greater than a melting point or softening temperature of the PVDF to disperse the GO-PVDF composite in the carrier fluid, wherein the GO-PVDF composite has a transmission FTIR minimum transmittance ratio of β-phase PVDF to α-phase PVDF of about 1 or less; cooling the mixture to below the melting point or softening temperature of the PVDF to form GO-PVDF particles; and separating the GO-PVDF particles from the carrier fluid, wherein the GO-PVDF particles comprise the graphene oxide dispersed in the PVDF, and wherein the GO-PVDF particles have a transmission FTIR minimum transmittance ratio of β-phase PVDF to α-phase PVDF of about 1 or less.

Composite materials are described herein. The composite materials include a polymer matrix comprising at least one fluorinated homo- or copolymer and continuous fibers dispersed within the polymer matrix. The continuous fibers are present within the composite material in an amount between about 10 wt % and about 90 wt % of a weight of the composite material. The composite materials also include a filler dispersed within the polymer matrix. The filler is present within the composite material in an amount between about 5 wt % and about 25 wt % of an amount of the polymer matrix.

Composite materials are described herein. The composite materials include a polymer matrix comprising at least one fluorinated homo- or copolymer and continuous fibers dispersed within the polymer matrix. The continuous fibers are present within the composite material in an amount between about 10 wt % and about 90 wt % of a weight of the composite material. The composite materials also include a filler dispersed within the polymer matrix. The filler is present within the composite material in an amount between about 5 wt % and about 25 wt % of an amount of the polymer matrix.

A fabrication method of a SERS substrate includes (a) preparing a hydrophilic membrane; (b) dipping the hydrophilic membrane in an alcohol; (c) immersing the hydrophilic membrane in a chloride ion aqueous solution; and (d) depositing Ag or Au nanoparticles on the hydrophilic membrane by suction filtration to form the SERS substrate. The hydrophilic membrane includes 10˜20 wt % PVDF, PTFE, PC, PES, nylon, or mixtures thereof, 10˜20 wt % PVP, and 0.2˜1.6 wt % PMMA, PHEMA, or mixtures thereof.