Abstract: A modified liquid diene rubber (A) has a functional group (a) derived from an acid anhydride, and satisfies all the requirements (I) to (III) below: (I) The functional group equivalent weight of the functional groups (a) is in the range of 400 to 3,500 g/eq. (II) The polystyrene-equivalent number average molecular weight (Mn) measured by gel permeation chromatography (GPC) is in the range of 5,000 to 20,000. (III) The melt viscosity at 38° C. is not less than 3 Pa·s and X (K) is not less than 6100 K wherein X is the slope of a linear line passing through two points in a graph in which the two points are values of melt viscosity ? (Pa·s) at 38° C. and 60° C. measured with a Brookfield viscometer which are plotted as Ln[?/(Pa·s)] on ordinate versus 1/T (K?1) on abscissa (with the proviso that T is temperature (K)).

Abstract: The present invention provides a rubber composition capable of giving cured products excellent in durability and vibration insulating properties. The present invention also provides a cured product of the composition, and a rubber vibration insulator using the cured product. The rubber composition includes a solid rubber (A), a liquid diene rubber (B), a silane coupling agent (C), and silica (D) having a BET specific surface area of 15 to 250 m2/g.

Abstract: A modified liquid diene rubber (A) has a functional group (a) derived from an acid anhydride, and satisfies all the requirements (I) to (III) below: (I) The functional group equivalent weight of the functional groups (a) is in the range of 400 to 3,500 g/eq. (II) The polystyrene-equivalent number average molecular weight (Mn) measured by gel permeation chromatography (GPC) is in the range of 5,000 to 20,000. (III) The melt viscosity at 38° C. is not less than 3 Pa·s and X (K) is not less than 6100 K wherein X is the slope of a linear line passing through two points in a graph in which the two points are values of melt viscosity ? (Pa·s) at 38° C. and 60° C. measured with a Brookfield viscometer which are plotted as Ln[?/(Pa·s)] on ordinate versus 1/T (K?1) on abscissa (with the proviso that T is temperature (K)).

Abstract: There are provided a modified liquid diene rubber that can be used for a curable resin composition and a resin composition containing the modified liquid diene rubber. The curable resin composition containing the modified liquid diene rubber has a much higher curing rate than that in the related art, and the resulting cured product has excellent mechanical properties, transparency, and heat resistance. Produced are a modified liquid diene rubber and a resin composition containing the modified liquid diene rubber. The modified liquid diene rubber includes a modifying group (p) partly containing a (meth)acryloyl group therein and a monomer unit (a1) derived from a conjugated diene compound. A carbon-carbon double bond derived from the conjugated diene compound has a hydrogenation rate of 30 to 95 mol %, and the modifying group (p) has a functional group equivalent weight of 700 to 20,000 g/eq.

Abstract: There are provided a modified liquid diene rubber that can be used for a curable resin composition and a resin composition containing the modified liquid diene rubber. The curable resin composition containing the modified liquid diene rubber has a much higher curing rate than that in the related art, and the resulting cured product has excellent mechanical properties, transparency, and heat resistance. Produced are a modified liquid diene rubber and a resin composition containing the modified liquid diene rubber. The modified liquid diene rubber includes a modifying group (p) partly containing a (meth)acryloyl group therein and a monomer unit (a1) derived from a conjugated diene compound. A carbon-carbon double bond derived from the conjugated diene compound has a hydrogenation rate of 30 to 95 mol %, and the modifying group (p) has a functional group equivalent weight of 700 to 20,000 g/eq.

Abstract: A modified liquid diene-based rubber (A) including, in a molecule, a modified group (a) containing a (meth)acryloyl group as a part thereof and at least one modified group (b) selected from a dicarboxylic acid monoester and a dicarboxylic acid monoamide, with the proviso that the modified group (b) comprises no (meth)acryloyl group as a part thereof, wherein the functional group equivalent weights of the modified group (a) and the modified group (b) are each in the range of 700 to 40,000 g/eq. Also provided is a curable resin composition containing the modified liquid diene-based rubber.

Abstract: Provided is a modified liquid diene-based rubber having an acryloyl group or a methacryloyl group, which is highly compatible with various monomers, such as acrylate or methacrylate having relatively high polarity, which can form a curable resin composition containing the modified liquid diene-based rubber with good workability, which has a satisfactory curing rate during curing, and which is capable of providing the curable resin composition that forms a cured product having excellent mechanical properties derived from the modified liquid diene-based rubber and having excellent adhesion to various materials. Also provided is a curable resin composition containing the modified liquid diene-based rubber.