Patent classifications
C08C19/12
MODIFIED DIENE-BASED POLYMER
An object of the present invention is to provide a diene-based polymer that can control the crosslinking morphology. The present invention provides a modified diene-based polymer having a structure represented by the formula (1).
##STR00001##
[In the formula (1), R.sup.1 and R.sup.2 represent an alkyl group having 1 or more carbon atoms, an aryl group having 6 or more carbon atoms, an aralkyl group having 6 or more carbon atoms, a hydrogen atom, or a halogen atom; and Z is an organic group, an organic group where a part of hydrogen atom of the above organic group is substituted, a hydrogen atom, or a halogen atom.]
VULCANIZED RUBBER SURFACE TREATMENT AGENT, METHOD OF PRODUCING ADHESIVE STRUCTURE, ADHESIVE STRUCTURE, AND TIRE
Provided is a vulcanized rubber surface treatment agent that enables firm adhesion between vulcanized rubbers without heating and has little effect on rubber deterioration. The vulcanized rubber surface treatment agent is used for adhering vulcanized rubbers to each other, which is an aqueous solution of hypochlorous acid having a pH value of 2 or more and 7 or less and an effective chlorine concentration of 100 ppm or more and 13000 ppm or less.
VULCANIZED RUBBER SURFACE TREATMENT AGENT, METHOD OF PRODUCING ADHESIVE STRUCTURE, ADHESIVE STRUCTURE, AND TIRE
Provided is a vulcanized rubber surface treatment agent that enables firm adhesion between vulcanized rubbers without heating and has little effect on rubber deterioration. The vulcanized rubber surface treatment agent is used for adhering vulcanized rubbers to each other, which is an aqueous solution of hypochlorous acid having a pH value of 2 or more and 7 or less and an effective chlorine concentration of 100 ppm or more and 13000 ppm or less.
Method for producing brominated and halohydrated polymers
Conjugated diene polymers such as a styrene-butadiene copolymer are sequentially brominated by reaction with a quaternary ammonium tribromide or quaternary phosphonium tribromide and halohydrated by reaction with an N-haloimide compound. This produces a brominated and halohydrated polymer with very good thermal stability. The product is useful as a flame retardant in a variety of polymer systems.
Method for producing brominated and halohydrated polymers
Conjugated diene polymers such as a styrene-butadiene copolymer are sequentially brominated by reaction with a quaternary ammonium tribromide or quaternary phosphonium tribromide and halohydrated by reaction with an N-haloimide compound. This produces a brominated and halohydrated polymer with very good thermal stability. The product is useful as a flame retardant in a variety of polymer systems.
CHEMICALLY RESISTANT FLUORINATED MULTIBLOCK POLYMER STRUCTURES, METHODS OF MANUFACTURING AND USE
Multi-block isoporous structures for non-aqueous and/or harsh chemical media having at least one of high separation specificity, chemical resistance, and antifouling properties, methods of manufacturing and use, for replacements or alternatives to existing separation membrane technologies.
Method of producing a conjugated diene polymer, a modified conjugated diene polymer, and a vinyl cis-polybutadiene composition
A method for producing a conjugated diene polymer having a high content of cis-1,4-structures with a high activity, a conjugated diene polymer, and a modified conjugated diene polymer. The catalyst for conjugated diene polymerization in the method includes: a non-metallocene type gadolinium compound (A) represented by the general formula (1); an ionic compound (B) formed of a non-coordinating anion and a cation; and an organic metal compound (C) of an element selected from the group consisting of a group 2, a group 12, and a group 13 of the periodic table.
Method of producing a conjugated diene polymer, a modified conjugated diene polymer, and a vinyl cis-polybutadiene composition
A method for producing a conjugated diene polymer having a high content of cis-1,4-structures with a high activity, a conjugated diene polymer, and a modified conjugated diene polymer. The catalyst for conjugated diene polymerization in the method includes: a non-metallocene type gadolinium compound (A) represented by the general formula (1); an ionic compound (B) formed of a non-coordinating anion and a cation; and an organic metal compound (C) of an element selected from the group consisting of a group 2, a group 12, and a group 13 of the periodic table.
Green chemistry method of synthesizing polymer structures that can function as a built-in antioxidant
A method of making a solid composition by reacting a tetrazine component and a polymer component through an inverse electron demand Diels-Alder reaction (IEDDA). The solid composition formed by the Diels-Alder reaction is in the form of either a foam or a powder depending on the functional groups of the tetrazine component. The polymer component can be various substituted polybutadienes, mixtures of stereoisomeric polydienes, and polybutadiene copolymers. The gas produced during the reaction is nitrogen, hence, the solid composition can be considered a greener material than polyurethanes, which involves carbon monoxide release during the course of the reaction. The aromatized polymer can act as a built in anti-oxidant with up to two hydrogen atom equivalents per dihydropyridazine group. The polymers of dihydropyridazines are converted to polymeric pyridazine groups by aromatization and the aromatic polymer becomes more stable.
Green chemistry method of synthesizing polymer structures that can function as a built-in antioxidant
A method of making a solid composition by reacting a tetrazine component and a polymer component through an inverse electron demand Diels-Alder reaction (IEDDA). The solid composition formed by the Diels-Alder reaction is in the form of either a foam or a powder depending on the functional groups of the tetrazine component. The polymer component can be various substituted polybutadienes, mixtures of stereoisomeric polydienes, and polybutadiene copolymers. The gas produced during the reaction is nitrogen, hence, the solid composition can be considered a greener material than polyurethanes, which involves carbon monoxide release during the course of the reaction. The aromatized polymer can act as a built in anti-oxidant with up to two hydrogen atom equivalents per dihydropyridazine group. The polymers of dihydropyridazines are converted to polymeric pyridazine groups by aromatization and the aromatic polymer becomes more stable.