Patent classifications
C08L27/04
Impact Strength Modifier for Chlorine-Containing Resin, Chlorine-Containing Resin Composition and Molded Body of Chlorine-Containing Resin Composition
Disclosed is an impact strength modifier (α) for a chlorine-containing resin, comprising a powder of a graft copolymer (A) obtained by graft polymerizing one or more kinds of vinyl monomers (b1) onto a polyorganosiloxane rubber (A1) or a composite rubber (A2) containing a polyorganosiloxane rubber and a polyalkyl (meth)acrylate rubber, wherein the specific surface area of the powder of the graft copolymer (A) measured by a nitrogen gas adsorption method is from 0.6 to 30 m.sup.2/g, and the pH of water used for extraction under conditions, in which (1) in an oven at 180° C., 5.0 g of the powder of the graft copolymer (A) is left to stand still and heated for 15 minutes, and (2) after the heating, the powder is dispersed in 100 ml of heated pure water and extracted for 1 hour at 70° C. while stirring, is from 4 to 11.
Impact Strength Modifier for Chlorine-Containing Resin, Chlorine-Containing Resin Composition and Molded Body of Chlorine-Containing Resin Composition
Disclosed is an impact strength modifier (α) for a chlorine-containing resin, comprising a powder of a graft copolymer (A) obtained by graft polymerizing one or more kinds of vinyl monomers (b1) onto a polyorganosiloxane rubber (A1) or a composite rubber (A2) containing a polyorganosiloxane rubber and a polyalkyl (meth)acrylate rubber, wherein the specific surface area of the powder of the graft copolymer (A) measured by a nitrogen gas adsorption method is from 0.6 to 30 m.sup.2/g, and the pH of water used for extraction under conditions, in which (1) in an oven at 180° C., 5.0 g of the powder of the graft copolymer (A) is left to stand still and heated for 15 minutes, and (2) after the heating, the powder is dispersed in 100 ml of heated pure water and extracted for 1 hour at 70° C. while stirring, is from 4 to 11.
COMPOSITE MATERIAL FROM WASTE AND AT LEAST ONE ELEMENT OF VULCANIZED RUBBER AND TIRE CORDS
The subject matter discloses a composite material comprising a first component and a second component, the first component comprising an organic element and a thermoplastic element and the second component comprising at least one element selected from the group consisting of vulcanized rubber and tire cords. The subject matter further discloses a process comprising mixing while heating under shear forces a first component comprising organic waste and thermoplastic waste with a second component comprising at least one element selected from the group consisting of vulcanized rubber and tire cords; to obtain a melt; processing the melt, the processing comprises at least cooling the melt to obtain a composite material comprising: organic element; thermoplastic element; and at least one element selected from the group consisting of vulcanized rubber and tire cords.
Resin composition and molded body formed therefrom
A novel vinyl chloride resin composition having exceptional transparency is provided. This resin composition comprises 3-15 parts by mass of a rubbery impact-absorbing material (B) for which the glass transition point in differential scanning calorimetry does not exceed 0° C., and 0.1-10 parts by mass of a lubricant (C) that satisfies (i)-(iv) below, the content amounts above being indicated relative to 100 parts by mass of a vinyl chloride resin (A) having a chlorine content of 55-75 mass %. (i) The melt viscosity at 200° C. is 5-5,000 mPa.Math.s (ii) The softening point is in the range of 60−180° C. (iii) The glass transition point (Tg) as measured in DSC is in the range of 0−100° C. (iv) A structural unit derived from at least one species selected from the group consisting of styrene, α-methylstyrene, indene, vinyl toluene, and isopropenyl toluene is contained in the molecule in an amount of 50-100 mass %
Resin composition and molded body formed therefrom
A novel vinyl chloride resin composition having exceptional transparency is provided. This resin composition comprises 3-15 parts by mass of a rubbery impact-absorbing material (B) for which the glass transition point in differential scanning calorimetry does not exceed 0° C., and 0.1-10 parts by mass of a lubricant (C) that satisfies (i)-(iv) below, the content amounts above being indicated relative to 100 parts by mass of a vinyl chloride resin (A) having a chlorine content of 55-75 mass %. (i) The melt viscosity at 200° C. is 5-5,000 mPa.Math.s (ii) The softening point is in the range of 60−180° C. (iii) The glass transition point (Tg) as measured in DSC is in the range of 0−100° C. (iv) A structural unit derived from at least one species selected from the group consisting of styrene, α-methylstyrene, indene, vinyl toluene, and isopropenyl toluene is contained in the molecule in an amount of 50-100 mass %
Method for low temperature bonding of elastomers
A method of bonding a vulcanized elastomer is provided comprising the steps of; providing an adhesive comprising a primary acrylate monomer, a reactive flexibilizing monomer, and further optionally comprising a toughener, an adhesion promoter and a free radical initiator, then depositing the adhesive on at least one surface of an elastomer or a second substrate, wherein the elastomer is a vulcanized elastomer, then bringing the elastomer substrate and second substrate together with the adhesive disposed therebetween, and allowing the adhesive to cure and bond the elastomer and second substrate together at a temperature of less than about 100° C. to produce a bonded structure.
Method for low temperature bonding of elastomers
A method of bonding a vulcanized elastomer is provided comprising the steps of; providing an adhesive comprising a primary acrylate monomer, a reactive flexibilizing monomer, and further optionally comprising a toughener, an adhesion promoter and a free radical initiator, then depositing the adhesive on at least one surface of an elastomer or a second substrate, wherein the elastomer is a vulcanized elastomer, then bringing the elastomer substrate and second substrate together with the adhesive disposed therebetween, and allowing the adhesive to cure and bond the elastomer and second substrate together at a temperature of less than about 100° C. to produce a bonded structure.
RESIN COMPOSITION
This invention relates to a resin composition comprising a resin component in an amount of 100 parts by weight, thermally expandable graphite in an amount of 3 to 300 parts by weight, and an inorganic filler in an amount of 2 to 200 parts by weight, wherein the expansion starting temperature of the thermally expandable graphite is lower than the decomposition starting temperature of the resin component.
RESIN COMPOSITION
This invention relates to a resin composition comprising a resin component in an amount of 100 parts by weight, thermally expandable graphite in an amount of 3 to 300 parts by weight, and an inorganic filler in an amount of 2 to 200 parts by weight, wherein the expansion starting temperature of the thermally expandable graphite is lower than the decomposition starting temperature of the resin component.
Moisture Curable Adhesive Compositions
A moisture curable composition, a method of applying the same, and a composition including the same are disclosed herein. In some embodiments, a curable composition, comprises: a component (A) having an organic polymer containing reactive silicon groups represented by the following general formula (1): —Si(R.sup.1.sub.3-a)X.sub.a (1) wherein R.sup.1 represents an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, or an aralkyl group having 7 to 20 carbon atoms, wherein X represents a hydrolyzable group, wherein each X is the same or different when two or more X are present, a is an integer from 1 to 3, when a is 1, each R.sup.1 may be the same or different, and when a is 2 or 3, each X may be the same or different; a component (B) having a chlorinated polyolefin polymer; and a component (C) having a carboxylic acid metal salt.