Patent classifications
C08F220/06
WATER-DISPERSED PRESSURE-SENSITIVE ADHESIVE COMPOSITION AND PRESSURE-SENSITIVE ADHESIVE SHEET
A water-dispersed pressure-sensitive adhesive composition of the present invention includes a water-dispersible polymer, a carboxylic acid copolymer thickener, a polyacrylic acid thickener, and water. A ratio of the carboxylic acid copolymer thickener in the solid content of the water-dispersed pressure-sensitive adhesive composition is 0.1% by mass or more and 1.5% by mass or less. A ratio of the polyacrylic acid thickener in the solid content of the adhesive composition is 1% by mass or more and 3.7% by mass or less. A pressure-sensitive adhesive sheet of the present invention has a pressure-sensitive adhesive layer formed from the water-dispersed pressure-sensitive adhesive composition.
LOW-DIELECTRIC RUBBER RESIN MATERIAL AND LOW-DIELECTRIC METAL SUBSTRATE
A low-dielectric rubber resin material and a low-dielectric metal substrate are provided. The rubber resin material includes a low-dielectric rubber resin composition and inorganic fillers. The low-dielectric rubber resin composition includes: 5 wt % to 40 wt % of a liquid rubber, 20 wt % to 70 wt % of a polyphenylene ether resin, 5 wt % to 30 wt % of a bismaleimide resin, and 20 wt % to 45 wt % of a crosslinker. A molecular weight of the liquid rubber ranges from 800 g/mol to 6000 g/mol. An iodine value of the liquid rubber ranges from 30 g/100 g to 60 g/100 g.
LOW-DIELECTRIC RUBBER RESIN MATERIAL AND LOW-DIELECTRIC METAL SUBSTRATE
A low-dielectric rubber resin material and a low-dielectric metal substrate are provided. The rubber resin material includes a low-dielectric rubber resin composition and inorganic fillers. The low-dielectric rubber resin composition includes: 5 wt % to 40 wt % of a liquid rubber, 20 wt % to 70 wt % of a polyphenylene ether resin, 5 wt % to 30 wt % of a bismaleimide resin, and 20 wt % to 45 wt % of a crosslinker. A molecular weight of the liquid rubber ranges from 800 g/mol to 6000 g/mol. An iodine value of the liquid rubber ranges from 30 g/100 g to 60 g/100 g.
Binder composition for non-aqueous electrolyte batteries, and binder aqueous solution for non-aqueous electrolyte batteries, slurry composition for non-aqueous electrolyte batteries, electrode for non-aqueous electrolyte batteries and non aqueous electrolyte battery each utilizing same
The present invention relates to a binder composition for a non-aqueous electrolyte battery, which is characterized by containing (A) polyvinyl alcohol, (B) at least one selected from a copolymer of vinyl alcohol and ethylenically unsaturated carboxylic acid and a neutralized salt of the copolymer and (C) at least one selected from an amino acid, a carboxylic acid-containing polymer and a polyamine; and a binder aqueous solution for a non-aqueous electrolyte battery, a slurry composition for a non-aqueous electrolyte battery, an electrode for a non-aqueous electrolyte battery, and a non-aqueous electrolyte battery, each containing the binder composition; and others.
Binder composition for non-aqueous electrolyte batteries, and binder aqueous solution for non-aqueous electrolyte batteries, slurry composition for non-aqueous electrolyte batteries, electrode for non-aqueous electrolyte batteries and non aqueous electrolyte battery each utilizing same
The present invention relates to a binder composition for a non-aqueous electrolyte battery, which is characterized by containing (A) polyvinyl alcohol, (B) at least one selected from a copolymer of vinyl alcohol and ethylenically unsaturated carboxylic acid and a neutralized salt of the copolymer and (C) at least one selected from an amino acid, a carboxylic acid-containing polymer and a polyamine; and a binder aqueous solution for a non-aqueous electrolyte battery, a slurry composition for a non-aqueous electrolyte battery, an electrode for a non-aqueous electrolyte battery, and a non-aqueous electrolyte battery, each containing the binder composition; and others.
Method for producing printed material and system for producing printed material
A method for producing a printed material includes providing pressure-induced phase transition particles on a recording medium having an arithmetic average roughness Ra of 0.07 μm or more and 3.80 μm or less to form a pressure-induced phase transition particle layer having a coverage C within a range of 30% to 90%; bonding the pressure-induced phase transition particles onto the recording medium; and folding the recording medium having the pressure-induced phase transition particles bonded thereon and pressure-bonding the folded recording medium, or pressure-bonding the recording medium having the pressure-induced phase transition particles bonded thereon and another recording medium placed on top of each other. The pressure-induced phase transition particles have at least two glass transition temperatures, and the difference between the lowest glass transition temperature and the highest glass transition temperature among the glass transition temperatures exhibited by the pressure-induced phase transition particles is 30° C. or more.
Method for producing printed material and system for producing printed material
A method for producing a printed material includes providing pressure-induced phase transition particles on a recording medium having an arithmetic average roughness Ra of 0.07 μm or more and 3.80 μm or less to form a pressure-induced phase transition particle layer having a coverage C within a range of 30% to 90%; bonding the pressure-induced phase transition particles onto the recording medium; and folding the recording medium having the pressure-induced phase transition particles bonded thereon and pressure-bonding the folded recording medium, or pressure-bonding the recording medium having the pressure-induced phase transition particles bonded thereon and another recording medium placed on top of each other. The pressure-induced phase transition particles have at least two glass transition temperatures, and the difference between the lowest glass transition temperature and the highest glass transition temperature among the glass transition temperatures exhibited by the pressure-induced phase transition particles is 30° C. or more.
Polymer emulsion and manufacturing method thereof
A method for manufacturing a polymer emulsion includes the following steps. A mixture is heated to a first temperature less than or equal to about 40° C. The mixture including about 100 to about 500 parts by weight of a monomer and about 0.5 to about 95 parts by weight of a first cross-linking agent, in which the monomer has a structure of formula (I): ##STR00001##
and R.sub.1, R.sub.2, and R.sub.3 represent H or C1-C4 alkyl group, respectively. About 0.005 to about 5 parts by weight of a first initiator is added. About 0.003 to about 5 parts by weight of a reducing agent is added to form an intermediate product. The intermediate product is heated to a second temperature less than or equal to about 92° C.
Polymer emulsion and manufacturing method thereof
A method for manufacturing a polymer emulsion includes the following steps. A mixture is heated to a first temperature less than or equal to about 40° C. The mixture including about 100 to about 500 parts by weight of a monomer and about 0.5 to about 95 parts by weight of a first cross-linking agent, in which the monomer has a structure of formula (I): ##STR00001##
and R.sub.1, R.sub.2, and R.sub.3 represent H or C1-C4 alkyl group, respectively. About 0.005 to about 5 parts by weight of a first initiator is added. About 0.003 to about 5 parts by weight of a reducing agent is added to form an intermediate product. The intermediate product is heated to a second temperature less than or equal to about 92° C.
Preparation method of super absorbent polymer
The present disclosure relates to a preparation method of a super absorbent polymer containing a novel cross-linking agent compound. The preparation method of a super absorbent polymer of the present disclosure can provide a super absorbent polymer exhibiting excellent absorption properties and an excellent deodorizing effect by including a cross-linking agent with a novel structure. Therefore, according to the present disclosure, since a separate additive for a deodorizing property is not required, processability and economic efficiency of the manufacturing process can be improved.