Patent classifications
C08C19/28
METHOD FOR PRODUCING CONJUGATED DIENE RUBBER
A method for producing conjugated diene rubber is provided, including: a first step of obtaining a conjugated diene polymer chain having an active end by polymerizing a monomer comprising a conjugated diene compound and a vinyl compound having a functional group interactive with silica using a polymerization initiator in an inert solvent; a second step of reacting a siloxane compound with the active end of the conjugated diene polymer chain having the active end; and a third step of reacting a hydrocarbyloxysilane compound with the conjugated diene polymer chain with which the siloxane compound has been reacted that is obtained in the second step.
METHOD FOR PRODUCING CONJUGATED DIENE RUBBER
A method for producing conjugated diene rubber is provided, including: a first step of obtaining a conjugated diene polymer chain having an active end by polymerizing a monomer comprising a conjugated diene compound and a vinyl compound having a functional group interactive with silica using a polymerization initiator in an inert solvent; a second step of reacting a siloxane compound with the active end of the conjugated diene polymer chain having the active end; and a third step of reacting a hydrocarbyloxysilane compound with the conjugated diene polymer chain with which the siloxane compound has been reacted that is obtained in the second step.
ZWITTERIONIC MONOMERS, POLYZWITTERIONIC POLYMERS FORMED THEREFROM, SURFACE FUNCTIONALIZATION AND SURFACE MODIFICATION
Disclosed herein are zwitterionic monomers, non-zwitterionic monomers, polyzwitterionic polymers formed therefrom; surface functionalization; surface modification; and articles containing any such compositions or surfaces formed therefrom.
ZWITTERIONIC MONOMERS, POLYZWITTERIONIC POLYMERS FORMED THEREFROM, SURFACE FUNCTIONALIZATION AND SURFACE MODIFICATION
Disclosed herein are zwitterionic monomers, non-zwitterionic monomers, polyzwitterionic polymers formed therefrom; surface functionalization; surface modification; and articles containing any such compositions or surfaces formed therefrom.
COMPOSITION COMPRISING THERMOASSOCIATIVE AND EXCHANGEABLE COPOLYMERS
Compositions resulting from the mixing of at least: a comb polydiol copolymer A1 and a compound A2 including at least two boronic ester functional groups, the comb polydiol copolymer A1 including a main chain and side chains, at least a portion of the side chains of the copolymer A1 being composed of oligomers. They exhibit very varied rheological properties depending on the proportion of the compounds A1 and A2 used. Composition resulting from the mixing of at least one lubricating oil with such a composition of associative and exchangeable polymers and use of this composition for lubricating a mechanical part.
POLYMERIC-INORGANIC NANOPARTICLE COMPOSITIONS, MANUFACTURING PROCESS THEREOF AND THEIR USE AS LUBRICANT ADDITIVES
The invention relates to polymeric-inorganic nanoparticle compositions and preparation processes thereof. The invention also relates to an additive and lubricant compositions comprising these polymeric-inorganic nanoparticle compositions, as well as to the use of these polymeric-inorganic nanoparticle compositions in an oil lubricant formulation to improve tribological performance, in particular to improve extreme pressure performance and friction reduction on metal parts.
RUBBER COMPOSITION FOR TIRE TREAD AND TIRE MANUFACTURED BY USING SAME
The present disclosure relates to a rubber composition for tire tread and a tire manufactured by using the same, and the rubber composition for tire tread improves rolling resistance and abrasion resistant performance and can improve handling and braking performances on a wet road surface and an ice and snow road surface at the same time by comprising 100 parts by weight of raw rubber and 70 to 120 parts by weight of a reinforcing filler, wherein the raw rubber includes 0 to 50 parts by weight of natural rubber, 20 to 100 parts by weight of a melt grafting-functionalized styrene butadiene rubber, and 0 to 30 parts by weight of butadiene rubber.
Modified Conjugated Diene-Based Polymer and Rubber Composition Including the Same
A modified conjugated diene-based polymer and a rubber composition including a modified conjugated diene-based polymer are disclosed herein. In some embodiments, a modified conjugated diene-based polymer includes a functional group derived from a modification initiator at one terminal and a functional group derived from a modifier represented by the Formula 2 or Formula 3 at the other terminal, wherein the modified conjugated diene-based polymer having a unimodal molecular weight distribution, and a polydispersity index of 1.0 to less than 1.7. The modified conjugated diene-based polymer prepared by continuous polymerization and having remarkable processability, narrow molecular weight distribution and excellent physical properties.
Modified Conjugated Diene-Based Polymer and Rubber Composition Including the Same
A modified conjugated diene-based polymer and a rubber composition including a modified conjugated diene-based polymer are disclosed herein. In some embodiments, a modified conjugated diene-based polymer includes a functional group derived from a modification initiator at one terminal and a functional group derived from a modifier represented by the Formula 2 or Formula 3 at the other terminal, wherein the modified conjugated diene-based polymer having a unimodal molecular weight distribution, and a polydispersity index of 1.0 to less than 1.7. The modified conjugated diene-based polymer prepared by continuous polymerization and having remarkable processability, narrow molecular weight distribution and excellent physical properties.
MODIFIED LIQUID DIENE RUBBERS
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.Math.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.Math.s) at 38 C. and 60 C. measured with a Brookfield viscometer which are plotted as Ln[/(Pa.Math.s)] on ordinate versus 1/T (K.sup.1) on abscissa (with the proviso that T is temperature (K)).