KR20220033928A - Modified conjugated diene-based polymer, preparing method thereof and rubber composition comprising the same - Google Patents

Abstract

The present invention relates to a modified conjugated diene-based polymer with remarkable processability and excellent tensile strength and viscoelastic properties, and a rubber composition comprising the same. The present invention provides the modified conjugated diene-based polymer which comprises: a first chain comprising a repeating unit derived from a conjugated diene-based monomer; a second chain comprising a repeating unit derived from a compound represented by chemical formula 1; and a unit derived from an amine-free alkoxysilane-based modifier, wherein the first chain and the second chain are coupled by a unit derived from a modifier.

Description

Modified conjugated diene-based polymer, manufacturing method thereof, and rubber composition comprising the same

The present invention relates to a modified conjugated diene-based polymer having excellent processability and excellent tensile strength and viscoelastic properties, a method for preparing the same, and a rubber composition comprising the same.

In response to the recent demand for fuel economy reduction in automobiles, a conjugated diene-based polymer having low rolling resistance, excellent abrasion resistance and tensile properties, and adjustment stability typified by wet road resistance is required as a rubber material for tires.

In order to reduce the rolling resistance of the tire, there is a method of reducing the hysteresis loss of the vulcanized rubber, and rebound elasticity of 50°C to 80°C, tan δ, Goodrich heat, etc. are used as evaluation indicators of the vulcanized rubber. That is, a rubber material having a large rebound elasticity at the above temperature or a small tan δ and Goodrich heat generation is preferable.

As a rubber material with a small hysteresis loss, natural rubber, polyisoprene rubber, polybutadiene rubber, etc. are known, but these have a problem of small wet road resistance. Accordingly, recently, conjugated diene-based polymers or copolymers such as styrene-butadiene rubber (hereinafter referred to as SBR) or butadiene rubber (hereinafter referred to as BR) have been manufactured by emulsion polymerization or solution polymerization and are used as rubber for tires. . Among them, the greatest advantage of solution polymerization compared to emulsion polymerization is that the content of vinyl structure and styrene content defining rubber properties can be arbitrarily adjusted, and molecular weight and physical properties can be adjusted by coupling or modification. that it can be adjusted. Therefore, it is easy to change the structure of the final manufactured SBR or BR, and it is possible to reduce the movement of the chain ends by bonding or modifying the chain ends, and to increase the binding force with fillers such as silica or carbon black. It is widely used as a rubber material for

When this solution-polymerized SBR is used as a rubber material for a tire, by increasing the vinyl content in the SBR, the glass transition temperature of the rubber can be increased to adjust the required physical properties of the tire, such as rolling resistance and braking force, as well as lower the glass transition temperature. By properly adjusting it, fuel consumption can be reduced. The solution polymerization SBR is prepared by using an anionic polymerization initiator, and a technique for introducing a functional group at the end by binding or modifying the chain end of the formed polymer using various modifiers is used. For example, U.S. Patent No. 4,397,994 discloses a technique in which an active anion at the chain end of a polymer obtained by polymerizing styrene-butadiene in a non-polar solvent using alkyllithium, a monofunctional initiator, is combined using a binder such as a tin compound. did

On the other hand, as a modifier for introducing a functional group into the chain terminal of a polymer, a technique of applying an aminoalkoxysilane modifier containing an alkoxysilane group and an amine group in a molecule at the same time in order to maximize the dispersibility and reactivity of the filler is widely known. However, as the number of amine groups in the modifier increases, the solubility in the hydrocarbon solvent used for preparing the polymer decreases, and thus there is a problem in that it is difficult to easily perform the modification reaction.

US 4397994 A

The present invention has been devised to solve the problems of the prior art, and has excellent affinity with a filler including a second chain including a repeating unit derived from the compound represented by Formula 1 and a unit derived from an amine-containing alkoxysilane-based modifier An object of the present invention is to provide a modified conjugated diene-based polymer.

In addition, the present invention includes a first chain of an active polymer and a second chain derived from a macromonomer, which are modified by reacting a macromonomer including a repeating unit derived from the compound represented by Formula 1 after the denaturation reaction, wherein the first chain An object of the present invention is to provide a method for producing the modified conjugated diene-based polymer in which a chain and a second chain are coupled by a modifier-derived unit.

In addition, an object of the present invention is to provide a rubber composition comprising the modified conjugated diene-based polymer.

According to one embodiment of the present invention for solving the above problems, the present invention provides a first chain comprising a repeating unit derived from a conjugated diene-based monomer; a second chain comprising a repeating unit derived from a compound represented by the following formula (1); and a unit derived from an amine-containing alkoxysilane-based modifier, wherein the first chain and the second chain are coupled by a modifier-derived unit to provide a modified conjugated diene-based polymer:

[Formula 1]

In Formula 1,

R _1a to R _1c are each independently a hydrogen atom; an alkyl group having 1 to 20 carbon atoms; an alkenyl group having 2 to 20 carbon atoms; an alkynyl group having 2 to 20 carbon atoms; A heteroalkyl group having 1 to 20 carbon atoms, a heteroalkenyl group having 2 to 20 carbon atoms; a heteroalkynyl group having 2 to 20 carbon atoms; a cycloalkyl group having 5 to 20 carbon atoms; an aryl group having 6 to 20 carbon atoms; Or a heterocyclic group having 3 to 20 carbon atoms,

R _1d is a single bond, an alkylene group having 1 to 20 carbon atoms that is unsubstituted or substituted with a substituent; a cycloalkylene group having 5 to 20 carbon atoms that is unsubstituted or substituted with a substituent; Or an arylene group having 6 to 20 carbon atoms substituted or unsubstituted with a substituent, wherein the substituent is an alkyl group having 1 to 10 carbon atoms, a cycloalkyl group having 5 to 10 carbon atoms, or an aryl group having 6 to 20 carbon atoms,

R _1f and R _1g are each independently a single bond, an alkylene group having 1 to 20 carbon atoms substituted or unsubstituted with a substituent; a cycloalkylene group having 5 to 20 carbon atoms that is unsubstituted or substituted with a substituent; Or an arylene group having 6 to 20 carbon atoms substituted or unsubstituted with a substituent, wherein the substituent is an alkyl group having 1 to 10 carbon atoms, a cycloalkyl group having 5 to 10 carbon atoms, or an aryl group having 6 to 20 carbon atoms,

R _1h, R _1i, R _1j and R _1k are each independently an alkyl group having 1 to 20 carbon atoms; an alkenyl group having 2 to 20 carbon atoms; an alkynyl group having 2 to 20 carbon atoms; a heteroalkyl group having 1 to 20 carbon atoms; a heteroalkenyl group having 2 to 20 carbon atoms; a heteroalkynyl group having 2 to 20 carbon atoms; a cycloalkyl group having 5 to 20 carbon atoms; an aryl group having 6 to 20 carbon atoms; or a heterocyclic group having 3 to 20 carbon atoms.

In addition, the present invention comprises the steps of preparing an active first chain by polymerizing a conjugated diene-based monomer or a conjugated diene-based monomer and an aromatic vinyl-based monomer in a hydrocarbon solvent in the presence of a polymerization initiator (S1); preparing a modified active first chain by reacting the active first chain with an amine-containing alkoxysilane-based modifier (S2); And it provides a method for producing the conjugated diene-based polymer comprising the step (S3) of reacting the modified active first chain with a macromonomer including a repeating unit derived from a compound represented by the following formula (1):

[Formula 1]

In Formula 1,

R _1a to R _1c are each independently a hydrogen atom; an alkyl group having 1 to 20 carbon atoms; an alkenyl group having 2 to 20 carbon atoms; an alkynyl group having 2 to 20 carbon atoms; A heteroalkyl group having 1 to 20 carbon atoms, a heteroalkenyl group having 2 to 20 carbon atoms; a heteroalkynyl group having 2 to 20 carbon atoms; a cycloalkyl group having 5 to 20 carbon atoms; an aryl group having 6 to 20 carbon atoms; Or a heterocyclic group having 3 to 20 carbon atoms,

R _1d is a single bond, an alkylene group having 1 to 20 carbon atoms that is unsubstituted or substituted with a substituent; a cycloalkylene group having 5 to 20 carbon atoms that is unsubstituted or substituted with a substituent; Or an arylene group having 6 to 20 carbon atoms substituted or unsubstituted with a substituent, wherein the substituent is an alkyl group having 1 to 10 carbon atoms, a cycloalkyl group having 5 to 10 carbon atoms, or an aryl group having 6 to 20 carbon atoms,

R _1f and R _1g are each independently a single bond, an alkylene group having 1 to 20 carbon atoms substituted or unsubstituted with a substituent; a cycloalkylene group having 5 to 20 carbon atoms that is unsubstituted or substituted with a substituent; Or an arylene group having 6 to 20 carbon atoms substituted or unsubstituted with a substituent, wherein the substituent is an alkyl group having 1 to 10 carbon atoms, a cycloalkyl group having 5 to 10 carbon atoms, or an aryl group having 6 to 20 carbon atoms,

R _1h, R _1i, R _1j and R _1k are each independently an alkyl group having 1 to 20 carbon atoms; an alkenyl group having 2 to 20 carbon atoms; an alkynyl group having 2 to 20 carbon atoms; a heteroalkyl group having 1 to 20 carbon atoms; a heteroalkenyl group having 2 to 20 carbon atoms; a heteroalkynyl group having 2 to 20 carbon atoms; a cycloalkyl group having 5 to 20 carbon atoms; an aryl group having 6 to 20 carbon atoms; or a heterocyclic group having 3 to 20 carbon atoms.

In addition, the present invention provides a rubber composition comprising the modified conjugated diene-based polymer and a filler.

The modified conjugated diene-based polymer according to the present invention is prepared by a manufacturing method comprising the step of reacting the modified active first chain with a macromonomer including a repeating unit derived from the compound represented by Formula 1 after the modification reaction, thereby derived from the modifier A functional group derived from the compound represented by Formula 1 in the polymer molecular chain may be included separately from the functional group used, and thus the affinity with the filler may be excellent.

The method for producing a modified conjugated diene-based polymer according to the present invention comprises reacting a macromonomer including a repeating unit derived from the compound represented by Formula 1 after the modification reaction, thereby adding the polymer represented by Formula 1 separately from the modifier A functional group derived from the compound, such as an amine group, may be introduced to prepare a highly modified conjugated diene-based polymer.

In addition, the rubber composition according to the present invention has excellent tensile properties and viscoelastic properties by including the modified conjugated diene-based polymer.

Hereinafter, the present invention will be described in more detail to help the understanding of the present invention.

The terms or words used in the description and claims of the present invention should not be construed as being limited to their ordinary or dictionary meanings, and the inventor must properly understand the concept of the term in order to best describe his invention. Based on the principle that can be defined, it should be interpreted as meaning and concept consistent with the technical idea of the present invention.

Definition of Terms

As used herein, the term 'macromonomer' may be combined with another polymer chain or a reactive compound through a unit in which two or more units derived from a polymerization-reactive monomer are repeated, or a terminal group.

As used herein, the term 'polymer' refers to a polymer compound prepared by polymerizing monomers, whether of the same or different type. The generic term polymer thus encompasses the terms homopolymer and copolymer, which are commonly used to refer to polymers prepared from only one monomer.

In the present specification, the term 'first chain (main chain)' may mean a molecular chain of a main backbone constituting a polymer, and a chain mainly including a conjugated diene-based monomer or a repeating unit of a conjugated diene-based monomer and an aromatic vinyl-based monomer. may mean, and the 'second chain (sub chain)' may refer to a chain having a smaller number of repeating units than the first chain and mainly including repeating units derived from the compound represented by Formula 1.

As used herein, the term 'vinyl content' refers to the mass (or weight) of butadiene contained in positions 1 and 2 in the polymer chain, based on the portion (total amount of polymerized butadiene) of the conjugated diene monomer (butadiene, etc.) in the polymer. ) refers to the percentage.

As used herein, the term 'monovalent hydrocarbon group' refers to a monovalent atomic group in which carbon and hydrogen are bonded, such as a monovalent alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, a cycloalkyl group containing one or more unsaturated bonds, and an aryl group. and the minimum number of carbon atoms of the substituent represented by the monovalent hydrocarbon may be determined according to the type of each substituent.

As used herein, the term 'divalent hydrocarbon group' refers to a divalent alkylene group, an alkenylene group, an alkynylene group, a cycloalkylene group, a cycloalkylene group including one or more unsaturated bonds, and an arylene group, such as carbon and hydrogen bonded 2 It may mean a valent atomic group, and the minimum number of carbon atoms of the substituent represented by the divalent hydrocarbon may be determined according to the type of each substituent.

As used herein, the term 'alkyl group' may refer to a monovalent aliphatic saturated hydrocarbon, and linear alkyl groups such as methyl, ethyl, propyl and butyl and isopropyl, sec-butyl, ter It may mean including all branched alkyl groups such as tert-butyl and neopentyl.

As used herein, the term 'alkenyl group' may refer to a monovalent aliphatic unsaturated hydrocarbon including one or two or more double bonds.

As used herein, the term 'alkynyl group' may mean a monovalent aliphatic unsaturated hydrocarbon including one or two or more triple bonds.

As used herein, the term 'alkylene group' may refer to a divalent aliphatic saturated hydrocarbon such as methylene, ethylene, propylene, and butylene.

In the present specification, the term 'aryl group' may mean an aromatic hydrocarbon, and also a monocyclic aromatic hydrocarbon in which one ring is formed, or a polycyclic aromatic hydrocarbon in which two or more rings are bonded (polycyclic aromatic hydrocarbon) may be meant to include all of them.

As used herein, the term 'heterocyclic group' refers to a carbon atom in a cycloalkyl group or an aryl group in which one or more hetero atoms are substituted, for example, it may mean including both a heterocycloalkyl group or a heteroaryl group.

As used herein, the term 'substitution' may mean that hydrogen of a functional group, atomic group, or compound is substituted with a specific substituent, and when hydrogen of a functional group, atomic group, or compound is substituted with a specific substituent, within the functional group, atomic group or compound One or two or more plural substituents may be present depending on the number of hydrogens present, and when plural substituents are present, each substituent may be the same or different from each other.

As used herein, the term 'single bond' may refer to a single covalent bond itself that does not include a separate atom or molecular group.

As used herein, the terms 'derived unit', 'derived repeating unit' and 'derived functional group' may refer to a component, structure, or material itself derived from a certain material.

The terms 'comprising', 'having' and their derivatives herein are not intended to exclude the presence of any additional component, step or procedure, whether or not they are specifically disclosed. . For the avoidance of any doubt, all compositions claimed through use of the term 'comprising', unless stated to the contrary, contain any additional additives, adjuvants, or compounds, whether polymeric or otherwise. may include In contrast, the term 'consisting essentially of' excludes from the scope of any subsequent description any other component, step or procedure, except as not essential to operability. The term 'consisting of' excludes any component, step or procedure not specifically described or listed.

Measurement method and conditions

In the present specification, the 'vinyl content' refers to the vinyl content in each polymer was measured and analyzed using Varian VNMRS 500 MHz NMR, and 1,1,2,2-tetrachloroethane was used as the solvent for NMR measurement. , the solvent peak is calculated as 6.0 ppm, 7.2-6.9 ppm is random styrene, 6.9-6.2 ppm is block styrene, 5.8-5.1 ppm is 1,4-vinyl and 1,2-vinyl, 5.1-4.5 ppm is 1, It is measured by calculating the content of 1,2-vinyl bonds in the entire polymer using the peak of 2-vinyl.

In the present specification, 'weight average molecular weight (Mw)', 'number average molecular weight (Mn)' and 'molecular weight distribution (MWD)' are measured through gel permeation chromatohraph (GPC) analysis, and measured by checking the molecular weight distribution curve. will be. Molecular weight distribution (PDI, MWD, Mw/Mn) is calculated from each of the measured molecular weights. Specifically, the GPC uses a combination of two PLgel Olexis (Polymer Laboratories) columns and one PLgel mixed-C (Polymer Laboratories) column, and when calculating molecular weight, the GPC reference material (Standard material) is PS (polystyrene) The GPC measurement solvent is prepared by mixing 2 wt% of an amine compound with tetrahydrofuran.

In the present specification, 'N atom content' may be, for example, measured through an NSX analysis method, and the NSX analysis method is measured using a trace nitrogen quantitative analyzer (NSX-2100H). Exemplarily, when using the trace nitrogen quantitative analyzer, turn on the trace nitrogen quantitative analyzer (Auto sampler, Horizontal furnace, PMT & Nitrogen detector), Ar at 250 ml/min, O ₂ at 350 ml/min, ozonizer 300 ml/ Set the carrier gas flow rate to min, set the heater to 800°C, and wait for about 3 hours to stabilize the analyzer. After the analyzer is stabilized, a calibration curve in the range of 5 ppm, 10 ppm, 50 ppm, 100 ppm and 500 ppm was prepared using Nitrogen standard (AccuStandard S-22750-01-5 ml), and the area corresponding to each concentration was obtained. Then, draw a straight line using the ratio of concentration to area. Thereafter, a ceramic boat containing 20 mg of the sample is placed on the auto sampler of the analyzer to obtain an area, and the N content is calculated using the area of the sample obtained and the calibration curve. At this time, the sample is a modified conjugated diene-based polymer in which the solvent is removed by putting it in hot water heated with steam and stirring, and the residual monomer, residual modifier, and oil are removed.

In the present specification, 'Si atom content' was measured using an inductively coupled plasma emission analyzer (ICP-OES; Optima 7300DV) as an ICP analysis method. Specifically, about 0.7 g of the sample is placed in a platinum crucible (Pt crucible), and about 1 mL of concentrated sulfuric acid (98 wt%, Electronic grade) is added, heated at 300° C. for 3 hours, and the sample is heated in an electric furnace (Thermo Scientific, Lindberg Blue M), after conducting conversation with the program of steps 1 to 3 below,

1) step 1: initial temp 0℃, rate (temp/hr) 180 ℃/hr, temp(holdtime) 180℃ (1hr)

2) step 2: initial temp 180℃, rate (temp/hr) 85 ℃/hr, temp(holdtime) 370℃ (2hr)

3) step 3: initial temp 370℃, rate (temp/hr) 47 ℃/hr, temp(holdtime) 510℃ (3hr)

1 mL of concentrated nitric acid (48 wt%) and 20 μl of concentrated hydrofluoric acid (50 wt%) were added to the residue, sealed in a platinum crucible and shaken for at least 30 minutes, and then 1 mL of boric acid was added to the sample. and stored at 0° C. for 2 hours or more, diluted in 30 mL of ultrapure water, and measured by incineration.

Modified conjugated diene-based polymer

The present invention provides a modified conjugated diene-based polymer capable of providing a rubber composition having excellent affinity with a filler and, as a result, excellent processability, tensile properties and viscoelastic properties.

The modified conjugated diene-based polymer according to an embodiment of the present invention includes a first chain including a repeating unit derived from a conjugated diene-based monomer; a second chain comprising a repeating unit derived from a compound represented by the following formula (1); and a unit derived from an amine-containing alkoxysilane-based modifier, wherein the first chain and the second chain are coupled to each other by a modifier-derived unit.

[Formula 1]

In Formula 1,

R _1a to R _1c are each independently a hydrogen atom; an alkyl group having 1 to 20 carbon atoms; an alkenyl group having 2 to 20 carbon atoms; an alkynyl group having 2 to 20 carbon atoms; A heteroalkyl group having 1 to 20 carbon atoms, a heteroalkenyl group having 2 to 20 carbon atoms; a heteroalkynyl group having 2 to 20 carbon atoms; a cycloalkyl group having 5 to 20 carbon atoms; an aryl group having 6 to 20 carbon atoms; Or a heterocyclic group having 3 to 20 carbon atoms,

R _1d is a single bond, an alkylene group having 1 to 20 carbon atoms that is unsubstituted or substituted with a substituent; a cycloalkylene group having 5 to 20 carbon atoms that is unsubstituted or substituted with a substituent; Or an arylene group having 6 to 20 carbon atoms substituted or unsubstituted with a substituent, wherein the substituent is an alkyl group having 1 to 10 carbon atoms, a cycloalkyl group having 5 to 10 carbon atoms, or an aryl group having 6 to 20 carbon atoms,

R _1f and R _1g are each independently a single bond, an alkylene group having 1 to 20 carbon atoms substituted or unsubstituted with a substituent; a cycloalkylene group having 5 to 20 carbon atoms that is unsubstituted or substituted with a substituent; Or an arylene group having 6 to 20 carbon atoms substituted or unsubstituted with a substituent, wherein the substituent is an alkyl group having 1 to 10 carbon atoms, a cycloalkyl group having 5 to 10 carbon atoms, or an aryl group having 6 to 20 carbon atoms,

R _1h, R _1i, R _1j and R _1k are each independently an alkyl group having 1 to 20 carbon atoms; an alkenyl group having 2 to 20 carbon atoms; an alkynyl group having 2 to 20 carbon atoms; a heteroalkyl group having 1 to 20 carbon atoms; a heteroalkenyl group having 2 to 20 carbon atoms; a heteroalkynyl group having 2 to 20 carbon atoms; a cycloalkyl group having 5 to 20 carbon atoms; an aryl group having 6 to 20 carbon atoms; or a heterocyclic group having 3 to 20 carbon atoms.

The modified conjugated diene-based polymer according to an embodiment of the present invention is a manufacturing method to be described later comprising the step of reacting a macromonomer including a repeating unit derived from the compound represented by Formula 1 with the modified active first chain after the modification reaction may be prepared by, through which the first chain including a repeating unit derived from a conjugated diene-based monomer and an amine-containing alkoxysilane-containing modifier-derived unit coupled to at least one terminal of the first chain derived from the macromonomer It may have the same structure as the graft copolymer to which the second chain is bonded. That is, the modified conjugated diene-based polymer may be one in which a first chain and a second chain are coupled by a unit derived from a modifier.

As such, when all of the functional groups are intensively distributed at one end of the modified conjugated diene-based polymer, only one end of the polymer binds to silica and the other end is free when interacting with silica, so the existing terminal end-modified polymer Similarly, the processability can be remarkably improved by showing an excellent effect on the dispersibility of the filler and the prevention of agglomeration. In addition, the second chain derived from the macromonomer and the modifier-derived unit are included at one end to which the functional group is bonded, so that the effect by interaction with the filler can be achieved at the same or higher level than that of the conventional modified polymer at both ends. Tensile properties and viscoelastic properties may be excellent.

In addition, in general, the modified conjugated diene-based polymer has a residue derived from the modifier, such as an alkoxy group (-OR, where R is a hydrocarbon group) or a hydroxyl group (-OH), and as time passes, a condensation reaction or Due to hydrolysis reaction, etc., storage stability is reduced, Mooney viscosity is increased, molecular weight distribution is increased, and thus excellent properties of the compounding properties of the modified conjugated diene-based polymer cannot be maintained, and the desired properties when applied to a rubber composition I have a problem I can't get. However, the modified conjugated diene-based polymer according to an embodiment of the present invention has a structure in which the second chain derived from the macromonomer is bonded to an alkoxy group, which is a residue derived from a modifier present in the polymer, by being prepared by the manufacturing method described below. As a result, the residue derived from the denaturant in the polymer does not exist or is reduced compared to the conventional manufacturing method.

In addition, the modified conjugated diene-based polymer according to an embodiment of the present invention has an advantage in that more functional groups can be introduced than when only a modifier having many functional groups is used by being prepared by the manufacturing method described later. Specifically, the alkoxy group of the active polymer and the modifier is difficult to bind two or more polymer chains to one molecule of the modifier due to steric hindrance of the polymer. must be insignificant. However, in the production method according to the present invention, the second chain derived from the macromonomer can bind the functional group to the alkoxy residue of the modifier to which the polymer chain is bonded, regardless of the steric hindrance as described above, so that the functional group in the polymer chain is further many can be introduced.

That is, the introduction of a functional group in one molecule of the modifier is clearly limited, and no matter how much is introduced, as in the present invention, when a chain containing a functional group is bonded to an alkoxy moiety without steric hindrance, it is an absolute functional group in the polymer. There is bound to be a difference in quantity.

Accordingly, the modified conjugated diene-based polymer according to the present invention has excellent storage stability over time, so that the compounding property can maintain uniformly excellent properties even after the initial stage of manufacture or over time, and tensile properties compared to conventional terminal-end modified polymers and excellent viscoelastic properties.

First chain comprising a repeating unit derived from a conjugated diene-based monomer

According to an embodiment of the present invention, the first chain serving as the main backbone of the modified conjugated diene-based polymer includes a repeating unit derived from a conjugated diene-based monomer, and the conjugated diene-based monomer includes 1,3-butadiene, 2,3 -Dimethyl-1,3-butadiene, piperylene, 3-butyl-1,3-octadiene, isoprene, 2-phenyl-1,3-butadiene and 2-halo-1,3-butadiene (halo is a halogen atom means) may be at least one selected from the group consisting of.

In addition, the first chain may further include a repeating unit derived from an aromatic vinyl-based monomer, and the aromatic vinyl-based monomer is styrene, α-methylstyrene, 3-methylstyrene, 4-methylstyrene, 4-propylstyrene, 1 -Vinylnaphthalene, 4-cyclohexylstyrene, 4-(p-methylphenyl)styrene, 1-vinyl-5-hexylnaphthalene, 3-(2-pyrrolidino ethyl)styrene (3-(2-pyrrolidino ethyl)styrene) , 4- (2-pyrrolidino ethyl) styrene (4- (2-pyrrolidino ethyl) styrene) and 3- (2-pyrrolidino-1-methyl ethyl) -α-methylstyrene (3- (2-pyrrolidino -1-methyl ethyl)-α-methylstyrene) may be at least one selected from the group consisting of.

As another example, the first chain of the modified conjugated diene-based polymer may be a copolymer further comprising a repeating unit derived from a diene-based monomer having 1 to 10 carbon atoms together with the repeating unit derived from the conjugated diene-based monomer. The repeating unit derived from the diene-based monomer may be a repeating unit derived from a diene-based monomer different from the conjugated diene-based monomer, and the diene-based monomer different from the conjugated diene-based monomer may be, for example, 1,2-butadiene. . When the modified conjugated diene-based polymer is a copolymer further comprising a diene-based monomer, the modified conjugated diene-based polymer contains more than 0% by weight to 1% by weight of the repeating unit derived from the diene-based monomer, more than 0% by weight to 0.1% by weight, It may contain more than 0 wt% to 0.01 wt%, or more than 0 wt% to 0.001 wt%, and has the effect of preventing gel formation within this range.

According to an embodiment of the present invention, when the first chain constituting the backbone of the modified conjugated diene-based polymer includes at least two monomer-derived repeating units, the first chain may be a random copolymer chain, and in this case, each There is an excellent effect of the balance between the physical properties. The random copolymer may mean that the repeating units constituting the copolymer are disorderly arranged.

A second chain comprising a repeating unit derived from a compound represented by Formula 1

In addition, the modified conjugated diene-based polymer according to an embodiment of the present invention further includes a second chain in addition to the first chain, and the second chain is a macromonomer including a repeating unit derived from a compound represented by Formula 1 Derived, the main unit may be a repeating unit derived from the compound represented by the formula (1).

Specifically, in Formula 1, R _1a to R _1c are each independently a hydrogen atom; an alkyl group having 1 to 10 carbon atoms; an alkenyl group having 2 to 10 carbon atoms; an alkynyl group having 2 to 10 carbon atoms; A heteroalkyl group having 1 to 10 carbon atoms, a heteroalkenyl group having 2 to 10 carbon atoms; a heteroalkynyl group having 2 to 10 carbon atoms; a cycloalkyl group having 5 to 10 carbon atoms; an aryl group having 6 to 12 carbon atoms; or a heterocyclic group having 3 to 10 carbon atoms, R _1d is a single bond or an unsubstituted alkylene group having 1 to 10 carbon atoms, R _1f and R _1g are each independently a single bond or unsubstituted alkyl having 1 to 10 carbon atoms a ren group, and R _1h, R _1i, R _1j and R _1k are each independently an alkyl group having 1 to 10 carbon atoms; an alkenyl group having 2 to 10 carbon atoms; an alkynyl group having 2 to 10 carbon atoms; a heteroalkyl group having 1 to 10 carbon atoms; a heteroalkenyl group having 2 to 10 carbon atoms; a heteroalkynyl group having 2 to 10 carbon atoms; a cycloalkyl group having 5 to 10 carbon atoms; an aryl group having 6 to 12 carbon atoms; Or it may be a heterocyclic group having 3 to 10 carbon atoms.

As another example, in Formula 1, R _1a to R _1c are each independently a hydrogen atom; or having 1 to 10 carbon atoms, R _1d is a single bond or an unsubstituted C 1 to C 6 alkylene group, R _1f and R _1g are each independently a single bond or an unsubstituted C 1 to C 6 alkylene group, R _1h, R _1i, R _1j and R _1k may each independently be an alkyl group having 1 to 10 carbon atoms.

More specifically, the compound represented by Formula 1 may be a compound represented by Formula 1-1 below.

[Formula 1-1]

Modifier: amine-containing alkoxysilane modifier

In addition, the modified conjugated diene-based polymer may be in a form in which a first chain and a second chain are coupled by a unit derived from an amine-containing alkoxysilane-based modifier, and the second chain may be coupled to the modifier as a hub. .

According to an embodiment of the present invention, the modifier may be a silica affinity modifier. The silica-affinity modifier may mean a modifier containing a silica-affinity functional group in a compound used as a modifier, and the silica-affinity functional group has excellent affinity with a filler, particularly a silica-based filler, It may mean a functional group capable of interaction between functional groups derived from the denaturant.

Specifically, according to an embodiment of the present invention, the amine-containing alkoxysilane-based modifier may be a compound represented by the following formula (2).

[Formula 2]

In Formula 2, R ¹ may be a single bond or an alkylene group having 1 to 10 carbon atoms, R ² and R ³ may each independently be an alkyl group having 1 to 10 carbon atoms, and R ⁴ is hydrogen, an epoxy group, or an alkylene group having 1 to 10 carbon atoms. It may be a monosubstituted, disubstituted or trisubstituted alkylsilyl group substituted with an alkyl group having 1 to 10 carbon atoms, an allyl group having 2 to 10 carbon atoms, an alkyl group having 1 to 10 carbon atoms, or a heterocyclic group having 2 to 10 carbon atoms, R ²¹ may be a single bond, an alkylene group having 1 to 10 carbon atoms, or -[R ⁴² O] _j -, R ⁴² may be an alkylene group having 1 to 10 carbon atoms, and a and m are each independently from 1 to 3 It may be an integer selected from, n may be an integer from 0 to 2, and j may be an integer selected from 1 to 30.

As a specific example, the compound represented by Formula 2 is N,N-bis(3-(dimethoxy(methyl)silyl)propyl)-methyl-1-amine(N,N-bis(3-(dimethoxy(methyl)silyl) )propyl)-methyl-1-amine), N,N-bis(3-(diethoxy(methyl)silyl)propyl)-methyl-1-amine (N,N-bis(3-(diethoxy(methyl)silyl) )propyl)-methyl-1-amine), N,N-bis(3-(trimethoxysilyl)propyl)-methyl-1-amine(N,N-bis(3-(trimethoxysilyl)propyl)-methyl- 1-amine), N,N-bis(3-(triethoxysilyl)propyl)-methyl-1-amine (N,N-bis(3-(triethoxysilyl)propyl)-methyl-1-amine), tri (trimethoxysilyl)amine), tri(3-(trimethoxysilyl)propyl)amine), N,N-bis(3- (diethoxy (methyl) silyl) propyl) -1,1,1-trimethylsilanamine (N, N-bis (3- (diethoxy (methyl) silyl) propyl) -1,1,1-trimethlysilanamine), N- (3-(1H-1,2,4-triazol-1-yl)propyl)-3-(trimethoxysilyl)-N-(3-(trimethoxysilyl)propyl)propan-1-amine ( N-(3-(1H-1,2,4-triazole-1-yl)propyl)-3-(trimethoxysilyl)-N-(trimethoxysilyl)propyl)propan-1-amine), 3-(trimethoxysilyl) )-N-(3-trimethoxysilyl)propyl)-N-(3-(1-(3-(trimethoxysilyl)propyl)-1H-1,2,4-triazol-3-yl) Propyl)propan-1-amine(3-(trimethoxysilyl)-N-(3-(trimethoxysilyl)propyl)-N-(3-(1-(3-(trimehtoxysilyl)propyl)-1H-1,2,4- triazol-3-yl)propyl)propan-1-amine), N-allyl-N-(3-(trimethoxysilyl)prop Phil)prop-2-en-1amine (N-allyl-N-(3-(trimethoxysilyl)propyl)prop-2-en-1-amine), N,N-bis(oxiran-2-ylmethyl) )-3-(trimethoxysilyl)propan 1-amine (N,N-bis(oxiran-2-ylmethyl)-3-(trimethoxysilyl)propan-1-amine), 1,1,1-trimethyl-N- (3- (triethoxysilyl) propyl) -N- (trimethylsilyl) silanamine (1,1,1-trimethyl-N- (3- (triethoxysilyl) propyl) -N- (trimethylsilyl) silanamine) and N; N-bis(3-(triethoxysilyl)propyl)-2,5,8,11,14-pentaoxahexadecan-16-amine (N,N-bis(3-(triethoxysilyl)propyl)-2, 5,8,11,14-pentaoxahexadecan-16-amine) may be one selected from the group consisting of.

As another example, the compound represented by Formula 2 may be at least one selected from compounds represented by Formulas 2-1 to 2-6 below.

[Formula 2-1]

[Formula 2-2]

[Formula 2-3]

[Formula 2-4]]

[Formula 2-5]

[Formula 2-6]

In Formulas 2-1 to 2-6, Me is a methyl group, and Et is an ethyl group.

As another example, the amine-containing alkoxysilane-based modifier may be a compound represented by the following formula (3).

[Formula 3]

또는

일 수 있으며, 이 때, R¹³, R¹⁴, R¹⁵ 및 R¹⁶은 각각 독립적으로 수소, 또는 탄소수 1 내지 10의 알킬기일 수 있다.In Formula 3, R ⁵ , R ⁶ and R ⁹ may each independently be an alkylene group having 1 to 10 carbon atoms, and R ⁷ , R ⁸ , R ¹⁰ and R ¹¹ are each independently an alkyl group having 1 to 10 carbon atoms. may be, R ¹² may be hydrogen or an alkyl group having 1 to 10 carbon atoms, b and c are each independently 1, 2 or 3, b+c≥4, and A is

or

may be, and in this case, R ¹³ , R ¹⁴ , R ¹⁵ and R ¹⁶ may each independently be hydrogen or an alkyl group having 1 to 10 carbon atoms.

As a specific example, the compound represented by Formula 3 is N-(3-(1H-imidazol-1-yl)propyl)-3-(triethoxysilyl)-N-(3-(triethoxysilyl)propyl Propan-1-amine (N-(3-(1H-imidazol-1-yl)propyl)-3-(triethoxysilyl)-N-(3-(triethoxysilyl)propyl)propan-1-amine) and 3-(4 ,5-dihydro-1H-imidazol-1-yl)-N,N-bis(3-(triethoxysilyl)propyl)propan-1-amine (3-(4,5-dihydro-1H-imidazol) It may be one selected from the group consisting of -1-yl)-N,N-bis(3-(triethoxysilyl)propyl)propan-1-amine).

As another example, the amine-containing alkoxysilane-based modifier may be a compound represented by the following formula (4).

[Formula 4]

In Formula 4, A ¹ and A ² may each independently be a divalent hydrocarbon group having 1 to 20 carbon atoms including or not including an oxygen atom, and R ¹⁷ to R ²⁰ are each independently a monovalent hydrocarbon group having 1 to 20 carbon atoms. may be a hydrocarbon group, and L ¹ to L ⁴ are each independently a monosubstituted, disubstituted or trisubstituted alkylsilyl group substituted with an alkyl group having 1 to 10 carbon atoms, or a monovalent hydrocarbon group having 1 to 20 carbon atoms, or L ¹ and L ² and L ³ and L ⁴ may be connected to each other to form a ring having 1 to 5 carbon atoms, and when L ¹ and L ² and L ³ and L ⁴ are connected to each other to form a ring, a ring formed may include 1 to 3 at least one hetero atom selected from the group consisting of N, O and S.

As a specific example, the compound represented by Formula 4 is 3,3'-(1,1,3,3-tetramethoxydisiloxane-1,3-diyl)bis(N,N-dimethylpropan-1-amine)( 3,3'-(1,1,3,3-tetramethoxydisiloxane-1,3-diyl)bis(N,N-dimethylpropan-1-amine), 3,3'-(1,1,3,3-tetra Ethoxydisiloxane-1,3-diyl)bis(N,N-dimethylpropan-1-amine)(3,3′-(1,1,3,3-tetraethoxydisiloxane-1,3-diyl)bis(N ,N-dimethylpropan-1-amine), 3,3'-(1,1,3,3-tetrapropoxydisiloxane-1,3-diyl)bis(N,N-dimethylpropan-1-amine)( 3,3'-(1,1,3,3-tetrapropoxydisiloxane-1,3-diyl)bis(N,N-dimethylpropan-1-amine), 3,3'-(1,1,3,3-tetra Methoxydisiloxane-1,3-diyl)bis(N,N-diethylpropan-1-amine)(3,3′-(1,1,3,3-tetramethoxydisiloxane-1,3-diyl)bis(N ,N-diethylpropan-1-amine), 3,3'-(1,1,3,3-tetramethoxydisiloxane-1,3-diyl)bis(N,N-dipropylpropan-1-amine) ( 3,3'-(1,1,3,3-tetramethoxydisiloxane-1,3-diyl)bis(N,N-dimpropylpropan-1-amine), 3,3'-(1,1,3,3-tetra Ethoxydisiloxane-1,3-diyl)bis(N,N-diethylpropan-1-amine)(3,3′-(1,1,3,3-tetraethoxydisiloxane-1,3-diyl)bis( N,N-diethylpropan-1-amine), 3,3'-(1,1,3,3-tetrapropoxydisiloxane-1,3-diyl)bis(N,N-diethylpropan-1-amine )(3,3'-(1,1,3,3-tetrapropoxydisiloxane-1,3-diyl)bis(N,N-diethylpropan-1-amine), 3,3'-(1,1,3,3 -tetraethoxydisiloxane-1,3-diyl)bis(N,N-dipropylpropan-1-amine) (3, 3'-(1,1,3,3-tetraethoxydisiloxane-1,3-diyl)bis(N,N-dipropylpropan-1-amine), 3,3'-(1,1,3,3-tetrapropoxy Cydisiloxane-1,3-diyl)bis(N,N-dipropylpropan-1-amine)(3,3′-(1,1,3,3-tetrapropoxydisiloxane-1,3-diyl)bis(N, N-dipropylpropan-1-amine), 3,3'-(1,1,3,3-tetramethoxydisiloxane-1,3-diyl)bis(N,N-diethylmethan-1-amine) (3 ,3'-(1,1,3,3-tetramethoxydisiloxane-1,3-diyl)bis(N,N-diethylmethan-1-amine), 3,3'-(1,1,3,3-tetrae Toxydisiloxane-1,3-diyl)bis(N,N-diethylmethan-1-amine)(3,3′-(1,1,3,3-tetraethoxydisiloxane-1,3-diyl)bis(N ,N-diethylmethan-1-amine), 3,3'-(1,1,3,3-tetrapropoxydisiloxane-1,3-diyl)bis(N,N-diethylmethan-1-amine) (3,3'-(1,1,3,3-tetrapropoxydisiloxane-1,3-diyl)bis(N,N-diethylmethan-1-amine), 3,3'-(1,1,3,3- Tetramethoxydisiloxane-1,3-diyl)bis(N,N-dimethylmethane-1-amine)(3,3′-(1,1,3,3-tetramethoxydisiloxane-1,3-diyl)bis(N ,N-dimethylmethan-1-amine), 3,3'-(1,1,3,3-tetramethoxydisiloxane-1,3-diyl)bis(N,N-dipropylmethan-1-amine) ( 3,3'-(1,1,3,3-tetramethoxydisiloxane-1,3-diyl)bis(N,N-dipropylmethan-1-amine), 3,3'-(1,1,3,3-tetra Propoxydisiloxane-1,3-diyl)bis(N,N-dimethylmethan-1-amine)(3,3′-(1,1,3,3-tetrapropoxydisiloxane-1,3-diyl)bis(N ,N-dimethylmethan-1-amine), 3,3'-(1,1,3, 3-tetrapropoxydisiloxane-1,3-diyl)bis(N,N-dipropylmethane-1-amine)(3,3'-(1,1,3,3-tetrapropoxydisiloxane-1,3-diyl )bis(N,N-dipropylmethan-1-amine), 3,3'-(1,1,3,3-tetraethoxydisiloxane-1,3-diyl)bis(N,N-dimethylmethane-1 -amine) (3,3'-(1,1,3,3-tetraethoxydisiloxane-1,3-diyl)bis(N,N-dimethylmethan-1-amine), 3,3'-(1,1,3 ,3-Tetraethoxydisiloxane-1,3-diyl)bis(N,N-dipropylmethane-1-amine)(3,3'-(1,1,3,3-tetraethoxydisiloxane-1,3-) diyl)bis(N,N-dipropylmethan-1-amine), N,N'-((1,1,3,3-tetramethoxydisiloxane-1,3-diyl)bis(propane-3,1-diyl) ))bis(1,1,1-trimethyl-N-(trimethylsilyl)silanamine(N,N'-((1,1,3,3-tetramethoxydisiloxane-1,3-diyl)bis(propan-3, 1-diyl))bis(1,1,1-trimethyl-N-(trimethylsilyl)silanamine), N,N'-((1,1,3,3-tetraethoxydisiloxane-1,3-diyl) Bis(propane-3,1-diyl))bis(1,1,1-trimethyl-N-(trimethylsilyl)silanamine(N,N'-((1,1,3,3-tetraethoxydisiloxane-1,3) -diyl)bis(propan-3,1-diyl))bis(1,1,1-trimethyl-N-(trimethylsilyl)silanamine), N,N'-((1,1,3,3-tetraprotoxy) Cydisiloxane-1,3-diyl)bis(propane-3,1-diyl))bis(1,1,1-trimethyl-N-(trimethylsilyl)silanamine(N,N'-((1,1, 3,3-tetrapropoxydisiloxane-1,3-diyl)bis(propan-3,1-diyl))bis(1,1,1-trimethyl-N-(trimethylsilyl)silanamine), N,N'-((1, 1,3,3-tetramethoxydisiloxane-1,3-diyl) Bis(propane-3,1-diyl))bis(1,1,1-trimethyl-N-phenylsilaneamine(N,N'-((1,1,3,3-tetramethoxydisiloxane-1,3-diyl) bis(propan-3,1-diyl))bis(1,1,1-trimethyl-N-phenylsilanamine), N,N'-((1,1,3,3-tetraethoxydisiloxane-1,3 -diyl)bis(propane-3,1-diyl))bis(1,1,1-trimethyl-N-phenylsilaneamine (N,N'-((1,1,3,3-tetraethoxydisiloxane-1,3) -diyl)bis(propan-3,1-diyl))bis(1,1,1-trimethyl-N-phenylsilanamine), N,N'-((1,1,3,3-tetrapropoxydisiloxane- 1,3-diyl)bis(propane-3,1-diyl))bis(1,1,1-trimethyl-N-phenylsilaneamine (N,N'-((1,1,3,3-tetrapropoxydisiloxane-) 1,3-diyl)bis(propan-3,1-diyl))bis(1,1,1-trimethyl-N-phenylsilanamine), 1,3-bis(3-(1H-imidazol-1-yl) propyl) 1,1,3,3-tetramethoxydisiloxane (1,3-bis(3-(1H-imidazol-1-yl)propyl)-1,1,3,3-tetramethoxydisiloxane), 1,3- Bis(3-(1H-imidazol-1-yl)propyl)1,1,3,3-tetraethoxydisiloxane(1,3-bis(3-(1H-imidazol-1-yl)propyl)- 1,1,3,3-tetraethoxydisiloxane), and 1,3-bis(3-(1H-imidazol-1-yl)propyl)1,1,3,3-tetrapropoxydisiloxane (1,3- It may be one selected from the group consisting of bis(3-(1H-imidazol-1-yl)propyl)-1,1,3,3-tetrapropoxydisiloxane).

More specifically, the compound represented by Chemical Formula 4 may be a compound represented by the following Chemical Formula 4-1.

[Formula 4-1]

In Formula 4-1, Me is a methyl group.

As another example, the amine-containing alkoxysilane-based modifier may be a compound represented by the following Chemical Formula 5.

[Formula 5]

In Formula 5, R _b2 to R _b4 are each independently an alkylene group having 1 to 10 carbon atoms, R _b5 to R _b8 are independently of each other an alkyl group having 1 to 10 carbon atoms, R _b13 and R _b14 are each independently a carbon number an alkylene group of 1 to 10, R _b15 to R _b18 are each independently an alkyl group having 1 to 10 carbon atoms, and m _{1 ,} m ₂ , m ₃ and m ₄ are each independently an integer of 1 to 3.

Specifically, the compound represented by the formula (5) may be a compound represented by the following formula (5-1).

[Formula 5-1]

In Formula 5-1, Et is an ethyl group.

As another example, the amine-containing alkoxysilane-based modifier may be a compound represented by the following formula (6).

[Formula 6]

In Formula 6, R _e1 and R _e2 are each independently an alkylene group having 1 to 10 carbon atoms, and _Re3 to R _e6 are independently hydrogen, an alkyl group having 1 to 10 carbon atoms, or -R _e7 SiR _e8 R _e9 R _e10 However, at least one of _Re3 to _Re6 is —R _e7 SiR _e8 Re9 _{Re9 Re10} , wherein _Re7 is a single bond or an alkylene group having 1 to 10 carbon atoms, and _Re8 to _Re10 are independently of each other 1 carbon number an alkyl group having 1 to 10 carbon atoms or an alkoxy group having 1 to 10 carbon atoms, wherein at least one of R _e8 to _Re10 is an alkoxy group having 1 to 10 carbon atoms.

Specifically, the compound represented by Chemical Formula 6 may be a compound represented by the following Chemical Formula 6-1.

[Formula 6-1]

In Formula 6-1, Me is a methyl group.

As another example, the amine-containing alkoxysilane-based modifier may be a compound represented by the following formula (7).

[Formula 7]

In Formula 7, R _h1 and R _h2 are each independently an alkyl group having 1 to 10 carbon atoms or an alkoxy group having 1 to 10 carbon atoms, R _h3 is a single bond or an alkylene group having 1 to 10 carbon atoms, A ₃ is -Si (R _h4 R _h5 R _h6 ) or —N[Si(R _h7 R _h8 R _h9 )] ₂ , wherein R _h4 to R _h9 are each independently an alkyl group having 1 to 10 carbon atoms or an alkoxy group having 1 to 10 carbon atoms. am.

Specifically, the compound represented by Formula 7 may be a compound represented by Formula 7-1 or Formula 7-2.

[Formula 7-1]

[Formula 7-2]

In Formulas 7-1 and 7-2, Me is a methyl group.

Main parameters of modified conjugated diene-based polymers

In addition, in the modified conjugated diene-based polymer according to an embodiment of the present invention, the content of N atoms in the polymer according to NSX analysis is 150 ppm or more by weight, and the content of Si atoms in the polymer according to ICP analysis is based on weight 50 ppm or more.

Specifically, in the modified conjugated diene-based polymer, the content of Si atoms in the polymer according to ICP analysis may be 70 ppm or more based on weight, preferably 100 ppm or more, and more preferably 150 ppm or more.

The content of Si atoms may be derived from a modifier, and in some cases, may be derived from a compound represented by Formula 1 and a modifier, and the content of Si atoms may be derived from a functional group present in the modified conjugated diene-based polymer, that is, a filler and As it can be expected to improve the affinity of

According to an embodiment of the present invention, in the modified conjugated diene-based polymer, the content of N atoms in the polymer according to NSX analysis may be 150 ppm or more, preferably 160 ppm or more, and more preferably 170 ppm or more. The modified conjugated diene-based polymer may have a relatively high content of N atoms by a manufacturing method in which a functional group derived from the compound represented by Formula 1, such as an amine group, is repeatedly present, and the functional group derived from the compound represented by Formula 1 is a polymer. By having one chain and a structure bonded to a modifier-derived unit bonded to at least one terminal of the first chain, affinity with a filler, such as silica, and dispersibility of silica in the compounding process are significantly improved, thereby providing excellent viscoelastic properties and at the same time Processability can be greatly improved.

In addition, due to the high content of N atoms, in the modified conjugated diene-based polymer according to an embodiment of the present invention, the molar ratio (N/Si) of N atoms to Si atoms may be 0.75 or more. In general, in the case of a polymer modified by a modifier, it may contain Si atoms and N atoms due to a modified polymerization initiator, a modified monomer, etc., but as described above, in the case of a polymer according to an embodiment of the present invention, as described above, Due to the inclusion of the indicated compound-derived repeating unit, the content of N atoms may be relatively large, and as a symbolic meaning thereof, the molar ratio of N atoms to Si atoms may be 0.75 or more, preferably 0.77 or more, or 0.78 or more , more preferably 0.8 or more, and most optimally 0.9 or more. Through this, it is possible to optimize the effect of improving processability according to the improvement of dispersibility during mixing.

Further, according to an embodiment of the present invention, the modified conjugated diene-based polymer has a Mooney viscosity change rate ( _MVR ) of 20% or less according to Equation 1 below.

[Equation 1]

MV _R = [(MV _f - MV _i ) / MV _i ] x 100

In Equation 1, MV _R is the Mooney viscosity change rate, MV _f is the 100° C. Mooney viscosity after the polymer is left at 25° C. for 30 days, and MV _i is the initial 100° C. Mooney viscosity of the polymer.

The Mooney viscosity change rate may be an indicator that not only processability but also a small increase in Mooney viscosity that occurs during storage after manufacturing is small. Due to the structural feature in which the second chain, the modifier-derived unit, and the first chain of the polymer are combined in a specific structure, processability is improved, and even when stored for a long time, the change rate of Mooney viscosity is low and storage stability can be excellent.

The Mooney viscosity change rate is the change rate of the initial Mooney viscosity of the polymer and the Mooney viscosity after the polymer is stored at room temperature for 30 days. In the present invention, the polymer is 20% or less, and preferably 15% or less. Here, the Mooney viscosity is 100° C. Mooney viscosity, and may be measured by a conventional method applied in the art.

General

As another example, the modified conjugated diene-based polymer according to an embodiment of the present invention has a number average molecular weight (Mn) of 1,000 g/mol to 2,000,000 g/mol, 10,000 g/mol to 1,000,000 g/mol, or 100,000 g/mol mol to 800,000 g/mol, and a weight average molecular weight (Mw) of 1,000 g/mol to 3,000,000 g/mol, 10,000 g/mol to 2,000,000 g/mol, or 100,000 g/mol to 2,000,000 g/mol, and , the peak average molecular weight (Mp) may be 1,000 g/mol to 3,000,000 g/mol, 10,000 g/mol to 2,000,000 g/mol, or 100,000 g/mol to 2,000,000 g/mol. Within this range, there is an excellent effect of rolling resistance and wet road resistance. As another example, the modified conjugated diene-based polymer may have a molecular weight distribution (PDI; MWD; Mw/Mn) of 1.0 or more to 3.0 or less, or 1.1 or more to 2.5 or less, or 1.1 or more and 2.0 or less, and tensile properties within this range and excellent viscoelastic properties, and excellent balance between physical properties.

In addition, the modified conjugated diene-based polymer may have a Mooney viscosity of 30 or more, 40 to 150, or 40 to 140 at 100° C., and has excellent processability and productivity within this range.

Here, the Mooney viscosity may be measured using a Mooney viscometer. Specifically, the polymer was left at room temperature (23±5°C) for more than 30 minutes at 100°C and a rotor speed of 2±0.02 rpm using a Monsanto’s MV2000E Large Rotor, and then 27±3 g was collected and inside the die cavity. It was measured while filling in the platen and applying a torque by operating the platen.

In addition, the modified conjugated diene-based polymer may have a vinyl content of 5 wt% or more, 10 wt% or more, or 10 wt% to 60 wt%. Here, the vinyl content means the content of the 1,2-added conjugated diene-based monomer, not the 1,4-added, based on 100% by weight of the conjugated diene-based copolymer consisting of a monomer having a vinyl group and an aromatic vinyl-based monomer. can

Method for producing a modified conjugated diene-based polymer

In addition, the present invention provides a method for producing the modified conjugated diene-based polymer.

The method for producing the modified conjugated diene-based polymer according to an embodiment of the present invention comprises polymerizing a conjugated diene-based monomer or a conjugated diene-based monomer and an aromatic vinyl-based monomer in a hydrocarbon solvent in the presence of a polymerization initiator to prepare an active first chain. step (S1); preparing a modified active first chain by reacting the active first chain with an amine-containing alkoxysilane-based modifier (S2); and reacting the modified active first chain with a macromonomer including a repeating unit derived from a compound represented by the following formula (1) (S3).

[Formula 1]

In Formula 1, R _1a to R _1k are the same as described above.

In addition, the modifier, the conjugated diene-based monomer and the aromatic vinyl-based monomer are the same as described above.

The hydrocarbon solvent is not particularly limited, but may be, for example, at least one selected from the group consisting of n-pentane, n-hexane, n-heptane, isooctane, cyclohexane, toluene, benzene and xylene.

The polymerization initiator is not particularly limited, for example, methyllithium, ethyllithium, propyllithium, isopropyllithium, n-butyllithium, s-butyllithium, t-butyllithium, hexyllithium, n-decyllithium, t-octyl Lithium, phenyllithium, 1-naphthyllithium, n-eicosyllithium, 4-butylphenyllithium, 4-tolylylithium, cyclohexyllithium, 3,5-di-n-heptylcyclohexyllithium, 4-cyclopentyllithium , sodium naphthyl, potassium naphthyl, lithium alkoxide, sodium alkoxide, potassium alkoxide, lithium sulfonate, sodium sulfonate, potassium sulfonate, lithium amide, sodium amide, potassium amide and lithium isopropylamide. may be more than

According to an embodiment of the present invention, the polymerization initiator is used in an amount of 0.01 mmol to 10 mmol, 0.05 mmol to 5 mmol, 0.1 mmol to 2 mmol, 0.1 mmol to 1 mmol, or 0.15 to 0.8 mmol based on 100 g of the total monomer. can be used Here, the total amount of 100 g of the monomer may represent a conjugated diene-based monomer or a total amount of a conjugated diene-based monomer and an aromatic vinyl-based monomer.

Step S1

The polymerization in step (S1) may be, for example, anionic polymerization, and as a specific example, living anionic polymerization having an anionic active site at the polymerization end by an anion-based growth polymerization reaction. In addition, the polymerization in step (S1) may be elevated temperature polymerization, isothermal polymerization, or constant temperature polymerization (adiabatic polymerization), and the constant temperature polymerization includes the step of polymerizing by its own heat of reaction without optionally applying heat after the polymerization initiator is added. may refer to a polymerization method, and the elevated temperature polymerization may refer to a polymerization method in which the temperature is increased by arbitrarily applying heat after the polymerization initiator is added, and the isothermal polymerization is heat by adding heat after the polymerization initiator is added It may refer to a polymerization method in which the temperature of the polymer is kept constant by increasing the temperature or taking heat away.

In addition, according to an embodiment of the present invention, the polymerization in step (S1) may be carried out by further including a diene-based compound having 1 to 10 carbon atoms in addition to the conjugated diene-based monomer. This has the effect of preventing the formation. An example of the diene-based compound may be 1,2-butadiene.

The polymerization of step (S1) may be carried out in a temperature range of, for example, less than 80 ℃, -20 ℃ to 80 ℃, 0 ℃ to 80 ℃, 0 ℃ to 70 ℃ or 10 ℃ to 70 ℃, within this range By narrowing the molecular weight distribution of the polymer, there is an excellent effect of improving physical properties.

The active polymer chain prepared by the step (S1) may refer to a polymer in which a polymer anion and an organometallic cation are bound.

Meanwhile, the polymerization in step (S1) may be carried out including a polar additive, and the polar additive is 0.001 g to 50 g, 0.001 g to 10 g, or 0.005 g to 0.1 g based on 100 g of the total monomer. It can be added in proportion. As another example, the polar additive may be added in a proportion of 0.001 g to 10 g, 0.005 g to 5 g, 0.005 g to 4 g based on 1 mmol of the polymerization initiator in total.

The polar additive is, for example, tetrahydrofuran, 2,2-di (2-tetrahydrofuryl) propane, diethyl ether, cyclopentyl ether, dipropyl ether, ethylene methyl ether, ethylene dimethyl ether, diethyl glycol, dimethyl ether , tert-butoxyethoxyethane, bis (3-dimethylaminoethyl) ether, (dimethylaminoethyl) ethyl ether, trimethylamine, triethylamine, tripropylamine, N,N,N',N'-tetra It may be at least one selected from the group consisting of methylethylenediamine, sodium mentholate, and 2-ethyl tetrahydrofurfuryl ether, preferably 2,2-di(2-tetra). It may be hydrofuryl) propane, triethylamine, tetramethylethylenediamine, sodium mentholate or 2-ethyl tetrahydrofurfuryl ether, and if the polar additive is included, it may be a conjugated diene In the case of copolymerizing the monomer-based monomer and the aromatic vinyl-based monomer, there is an effect of compensating for the difference in their reaction rate, thereby inducing the easy formation of a random copolymer.

Step S2

Step (S2) is a step for preparing a modified active first chain by reacting the active first chain with an amine-containing alkoxysilane-based modifier, wherein the reaction may be a modification or a coupling reaction, in which case, the The denaturant may be used in an amount of 0.01 mmol to 10 mmol based on 100 g of the total monomer. As another example, the modifier may be used in a molar ratio of 1:0.1 to 10, 1:0.1 to 5, or 1:0.1 to 1:3 based on 1 mole of the polymerization initiator in step (S1).

Step S3

In addition, the step (S3) is a step for preparing a modified conjugated diene-based polymer by reacting the active first chain with a macromonomer including a repeating unit derived from the compound represented by Formula 1.

On the other hand, the preparation method according to an embodiment of the present invention may further include the step of preparing a macromonomer before the step (S3), and the step of preparing the macromonomer is a chemical formula in the presence of an organolithium compound in a hydrocarbon solvent. a compound represented by 1; Alternatively, it may be carried out by polymerizing the compound represented by Formula 1 and a conjugated diene-based monomer. In this case, the polymerization reaction may be a living anionic polymerization having an anionic active site at the polymerization end by a growth polymerization reaction by an anion, and thus, the macromonomer may be a living anionic end capable of functioning as a monomer at one end.

Here, the organolithium compound may be an alkyllithium compound, and specifically, methyllithium, ethyllithium, propyllithium, isopropyllithium, n-butyllithium, s-butyllithium, t-butyllithium, hexyllithium, n -decyllithium, t-octyllithium, phenyllithium, 1-naphthyllithium, n-eicosyllithium, 4-butylphenyllithium, 4-tolylithium, cyclohexyllithium, 3,5-di-n-heptylcyclohexyl lithium or 4-cyclopentyllium, more specifically n-butyllithium.

For example, the macromonomer may be prepared through the following Reaction Scheme 1, and may be a compound having a structure represented by the following Chemical Formula M.

[Scheme 1]

In Scheme 1, R _1f to R _1k are as defined in Formula 1, R-Li is an alkyllithium compound, and R is an alkyl group derived from the alkyllithium.

In addition, the macromonomer includes 1 to 80, 1 to 60, or 1 to 50 repeating units derived from the compound represented by Formula 1, for example, in Formula M, r is 1 to 80, 1 to 60, or 1 to 50. In this case, the processability, tensile properties, and viscoelastic properties of the modified conjugated diene-based polymer including the second chain derived from the macromonomer may be excellent in a well-balanced manner.

Meanwhile, in step (S3), the modified active polymer and the macromonomer react with a functional group derived from the modifier in the modified active polymer and the living anion terminal of the macromonomer to prepare a modified conjugated diene-based polymer.

Specifically, the modified active polymer chain prepared in step (S2) includes a denaturant-derived functional group, and the denaturant-derived functional group includes an alkoxy group remaining without reacting with the polymer chain, and thus the living anion of the macromonomer By reacting the terminal and the alkoxy group, the modified conjugated diene-based polymer may be prepared.

In addition, the macromonomer may be used in an amount of 0.1 to 4.0 moles, 0.1 to 2.0 moles, or 0.5 to 1.5 moles relative to 1 mole of the polymerization initiator.

On the other hand, conventionally, as a method for introducing additional functional groups into the polymer, a condensation reaction in which an active polymer is modified with a modifier and then a compound capable of condensation with the Si-O bond of the modifier is reacted has been applied. However, when the condensation reaction is used in this way, the bond between the material having an additional functional group and the modified active polymer is formed as -Si-O-Si-, and hydrolysis may occur during the steam stripping step, washing step, or storage. , and thus there is a problem in that the bond is separated at the condensed binding site, and consequently a problem in which a functional group is lost.

On the other hand, in the case of the modified conjugated diene-based polymer prepared by the production method according to the present invention, the living end of the macromonomer reacts with the Si-OR group of the modifier to form a Si-C bond, which is hydrolyzed like a condensed bond. Since it is a bond in which no reaction occurs, there is no fear of separation, and thus storage stability is improved and there is no problem of loss of the first introduced functional group.

rubber composition

In addition, the present invention provides a rubber composition comprising the modified conjugated diene-based polymer.

The rubber composition may include the modified conjugated diene-based polymer in an amount of 10% by weight or more, 10% to 100% by weight, or 20% to 90% by weight, within this range, tensile strength, abrasion resistance, etc. It has excellent mechanical properties and excellent balance between the physical properties.

In addition, the rubber composition may further include other rubber components as needed in addition to the modified conjugated diene-based polymer, wherein the rubber component may be included in an amount of 90% by weight or less based on the total weight of the rubber composition. As a specific example, the other rubber component may be included in an amount of 1 to 900 parts by weight based on 100 parts by weight of the modified conjugated diene-based polymer.

The rubber component may be, for example, natural rubber or synthetic rubber, and specific examples thereof include natural rubber (NR) including cis-1,4-polyisoprene; Modified natural rubbers such as epoxidized natural rubber (ENR), deproteinized natural rubber (DPNR), and hydrogenated natural rubber that are modified or refined of the general natural rubber; Styrene-butadiene copolymer (SBR), polybutadiene (BR), polyisoprene (IR), butyl rubber (IIR), ethylene-propylene copolymer, polyisobutylene-co-isoprene, neoprene, poly(ethylene-co-) propylene), poly(styrene-co-butadiene), poly(styrene-co-isoprene), poly(styrene-co-isoprene-co-butadiene), poly(isoprene-co-butadiene), poly(ethylene-co-propylene) -co-diene), polysulfide rubber, acrylic rubber, urethane rubber, silicone rubber, epichlorohydrin rubber, or a synthetic rubber such as halogenated butyl rubber, and any one or a mixture of two or more thereof may be used.

The rubber composition may include, for example, 0.1 parts by weight to 200 parts by weight, or 10 parts by weight to 120 parts by weight of a filler based on 100 parts by weight of the modified conjugated diene-based polymer of the present invention. The filler may be, for example, a silica-based filler, and specific examples include wet silica (hydrous silicic acid), fumed silica (silicic anhydride), calcium silicate, aluminum silicate or colloidal silica, and preferably, the effect of improving fracture properties and wet It may be wet silica that has the best effect of compatibility with wet grip. In addition, the rubber composition may further include a carbon black-based filler if necessary.

As another example, when silica is used as the filler, a silane coupling agent for improving reinforcing properties and low heat generation may be used together, and as a specific example, the silane coupling agent is bis(3-triethoxysilylpropyl)tetrasulfide , bis(3-triethoxysilylpropyl)trisulfide, bis(3-triethoxysilylpropyl)disulfide, bis(2-triethoxysilylethyl)tetrasulfide, bis(3-trimethoxysilyl) propyl) tetrasulfide, bis(2-trimethoxysilylethyl)tetrasulfide, 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, 2-mercaptoethyltrimethoxysilane, 2-Mercaptoethyltriethoxysilane, 3-trimethoxysilylpropyl-N,N-dimethylthiocarbamoyltetrasulfide, 3-triethoxysilylpropyl-N,N-dimethylthiocarbamoyltetrasulfide Feed, 2-triethoxysilylethyl-N,N-dimethylthiocarbamoyltetrasulfide, 3-trimethoxysilylpropylbenzothiazolyltetrasulfide, 3-triethoxysilylpropylbenzolyltetrasulfide, 3-triethoxysilylpropylmethacrylate monosulfide, 3-trimethoxysilylpropylmethacrylate monosulfide, bis(3-diethoxymethylsilylpropyl)tetrasulfide, 3-mercaptopropyldimethoxymethyl It may be silane, dimethoxymethylsilylpropyl-N,N-dimethylthiocarbamoyltetrasulfide or dimethoxymethylsilylpropylbenzothiazolyltetrasulfide, and any one or a mixture of two or more thereof may be used. Preferably, in consideration of the reinforcing improvement effect, it may be bis(3-triethoxysilylpropyl)polysulfide or 3-trimethoxysilylpropylbenzothiazyltetrasulfide.

In addition, in the rubber composition according to an embodiment of the present invention, as a rubber component, a modified conjugated diene-based polymer in which a functional group with high affinity for silica is introduced is used as a rubber component, so the compounding amount of the silane coupling agent is conventional. may be reduced than the case, and accordingly, the silane coupling agent may be used in an amount of 1 to 20 parts by weight, or 5 to 15 parts by weight, based on 100 parts by weight of silica, and the effect as a coupling agent within this range is It has the effect of preventing the gelation of the rubber component while being sufficiently exhibited.

The rubber composition according to an embodiment of the present invention may be crosslinkable with sulfur, and may further include a vulcanizing agent. The vulcanizing agent may be specifically sulfur powder, and may be included in an amount of 0.1 to 10 parts by weight based on 100 parts by weight of the rubber component, and within this range, the vulcanized rubber composition has a low fuel efficiency while securing the required elasticity modulus and strength. It has an excellent effect.

The rubber composition according to an embodiment of the present invention includes, in addition to the above components, various additives commonly used in the rubber industry, specifically, a vulcanization accelerator, process oil, antioxidant, plasticizer, anti-aging agent, scorch inhibitor, zinc white), stearic acid, a thermosetting resin, or a thermoplastic resin may be further included.

The vulcanization accelerator is, for example, a thiazole-based compound such as M (2-mercaptobenzothiazole), DM (dibenzothiazyl disulfide), CZ (N-cyclohexyl-2-benzothiazyl sulfenamide), or DPG A guanidine-based compound such as (diphenylguanidine) may be used, and may be included in an amount of 0.1 to 5 parts by weight based on 100 parts by weight of the rubber component.

The process oil acts as a softener in the rubber composition, and may be, for example, a paraffinic, naphthenic, or aromatic compound. A naphthenic or paraffinic process oil may be used. The process oil may be included in an amount of 100 parts by weight or less based on 100 parts by weight of the rubber component, for example, and has an effect of preventing deterioration of the tensile strength and low heat generation (low fuel efficiency) of the vulcanized rubber within this range.

The antioxidant is, for example, 2,6-di-t-butylparacresol, dibutylhydroxytoluenyl, 2,6-bis((dodecylthio)methyl)-4-nonylphenol (2,6-bis( (dodecylthio)methyl)-4-nonylphenol) or 2-methyl-4,6-bis((octylthio)methyl)phenol (2-methyl-4,6-bis((octylthio)methyl)phenol), It may be used in an amount of 0.1 to 6 parts by weight based on 100 parts by weight of the rubber component.

The antioxidant is, for example, N-isopropyl-N'-phenyl-p-phenylenediamine, N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine, 6-ethoxy-2 ,2,4-trimethyl-1,2-dihydroquinoline, or a high-temperature condensate of diphenylamine and acetone, etc., may be used in an amount of 0.1 to 6 parts by weight based on 100 parts by weight of the rubber component.

The rubber composition according to an embodiment of the present invention can be obtained by kneading using a kneader such as a Banbury mixer, a roll, an internal mixer, etc. according to the compounding prescription, and has low heat generation and wear resistance by a vulcanization process after molding processing. This excellent rubber composition can be obtained.

Accordingly, the rubber composition may be used for each member of the tire such as a tire tread, under tread, side wall, carcass coated rubber, belt coated rubber, bead filler, cheffer, or bead coated rubber, vibration proof rubber, belt conveyor, hose, etc. It may be useful in the manufacture of various industrial rubber products of

In addition, the present invention provides a tire manufactured using the rubber composition.

The tire may include a tire or a tire tread.

Example

Hereinafter, examples will be given to describe the present invention in detail. However, the embodiment according to the present invention may be modified in various other forms, and the scope of the present invention should not be construed as being limited to the embodiment described in detail below. The embodiments of the present invention are provided to more completely explain the present invention to those of ordinary skill in the art.

production example

Put 100 ml of tetrahydrofuran and 1 g (10 wt% in n-hexane) of tetrahydrofuran and 1 g (10 wt% in n-hexane) in a 500 ml round-bottom flask, and 1,1'-(5-vinyl-1,3-phenylene)bis(N ,N-dimethylmethanamine) (1,1'-(5-vinyl-1,3-phenylene)bis(N,N-dimethylmethanamine) was added ([act. Li] 1 mole to 3 mole ratio), and then 10 A solution containing a macromonomer (15.6 mmol/l) was prepared by reacting at ℃ for 30 minutes, and after reaction through GC analysis, 1,1'-(5-vinyl-1,3-phenylene)bis(N, N-dimethylmethanamine) was not detected, confirming that the reaction was carried out.

Example 1

In a 20 L autoclave reactor, 3 kg of n-hexane, 215 g of styrene, 745 g of 1,3-butadiene and 1.29 g of 2,2-bis(2-oxolanyl)propane as a polar additive were added, followed by n-butyl Lithium 3.2 g (10wt% in n-hexane) was added, the internal temperature of the reactor was adjusted to 60° C., and an adiabatic temperature rising reaction was performed. After about 30 minutes, 39 g of 1,3-butadiene was added to cap the end of the polymer with butadiene, and after about 10 minutes, N,N-diethyl-3-(trimethoxysilyl)propane-1- with a modifier Amine (N,N-diethyl-3-(trimethoxysilyl)propan-1-amine) was added and reacted for 15 minutes ([DTP]:[act. Li]=1.5:1 molar ratio, [denaturant]:[act. Li] = 1:1 molar ratio). Then, the solution containing the macromonomer prepared in Preparation Example was added and reacted for 15 minutes ([act. Li]:[macromonomer] = 1:1 molar ratio), the reaction was stopped using ethanol, and the antioxidant 33 g of a solution in which Wingstay K was dissolved in hexane at 30% by weight was added. The resulting polymer was put into hot water heated by steam, stirred to remove the solvent, and then roll-dried to remove the remaining solvent and water to prepare a modified styrene-butadiene copolymer.

Example 2

In Example 1, N-allyl-N-(3-(trimethoxysilyl)propyl)prop- in place of N,N-diethyl-3-(trimethoxysilyl)propan-1-amine as a modifier Modified styrene was carried out in the same manner as in Example 1 except that 2-en-1-amine (N-allyl-N-(3-(trimethoxysilyl)propyl)prop-2-en-1-amine) was added. -Butadiene copolymer was prepared ([modifier]:[act. Li]=1:1 molar ratio).

Example 3

In Example 1, N-methyl-3-(trimethoxysilyl)-N-(3-(tri Methoxysilyl) propyl) propan-1-amine (N-methyl-3- (trimethoxysilyl) -N- (3- (trimethoxysilyl) propyl) propan-1-amine) in Example 1, except that In the same manner, a modified styrene-butadiene copolymer was prepared ([modifier]:[act. Li] = 1:1 molar ratio).

Example 4

In Example 1, N,N-bis(3-(triethoxysilyl)propyl)-3,6 instead of N,N-diethyl-3-(trimethoxysilyl)propan-1-amine as denaturant ,9,12,15-pentaoxanonadecan-1-amine (N,N-bis(3-(triethoxysilyl)propyl)-3,6,9,12,15-pentaoxanonadecan-1-amine) Except for that, a modified styrene-butadiene copolymer was prepared in the same manner as in Example 1 ([modifier]:[act. Li]=1:1 molar ratio).

Comparative Example 1

In Example 1, instead of n-butyllithium, a solution containing the macromonomer prepared in Preparation Example was added in an amount such that n-butyllithium of Example 1 and the macromonomer were equimolar to proceed with an adiabatic temperature rise reaction, , a modified styrene-butadiene copolymer was prepared in the same manner as in Example 1, except that the reaction was stopped after capping the butadiene without adding and reacting the modifier and the macromonomer.

Comparative Example 2

In a 20 L autoclave reactor, 3 kg of n-hexane, 215 g of styrene, 745 g of 1,3-butadiene and 1.29 g of 2,2-bis(2-oxoranyl)propane as a polar additive were added, followed by n-butyllithium 3.2 g (10 wt% in n-hexane) was adjusted to 60° C. inside the reactor and an adiabatic temperature rising reaction was carried out. After about 30 minutes, 39 g of 1,3-butadiene was added to cap the end of the polymer with butadiene, and after about 10 minutes, N,N-diethyl-3-(trimethoxysilyl)propane-1- with a modifier An amine was added and reacted for 15 minutes ([DTP]:[act. Li]=1.5:1 molar ratio, [modifier]:[act. Li]=1:1 molar ratio). Then, the reaction was stopped using ethanol, and 33 g of a solution in which an antioxidant, Wingstay K, was dissolved in hexane at 30% by weight was added. The resulting polymer was put into hot water heated with steam, stirred to remove the solvent, and then roll-dried to remove the remaining solvent and water to prepare a modified styrene-butadiene copolymer.

Comparative Example 3

In Comparative Example 2, instead of n-butyllithium, a solution containing the macromonomer prepared in Preparation Example was added in an amount such that n-butyllithium of Comparative Example 2 and the macromonomer were equimolar to proceed with an adiabatic temperature increase reaction. A modified styrene-butadiene copolymer was prepared in the same manner as in Comparative Example 2 except for the above.

Comparative Example 4

In a 20 L autoclave reactor, 3 kg of n-hexane, 215 g of styrene, 745 g of 1,3-butadiene, 1,1'-(5-vinyl-1,3-phenylene)bis(N,N-) as a modified monomer After adding 1.29 g of dimethylmethanamine) ([act. Li]:[modified monomer] = 1:2 molar ratio) and 2,2-bis(2-oxoranyl)propane as a polar additive, n-butyllithium 3.2 g (10 wt% in n-hexane) was adjusted to 60° C. inside the reactor and an adiabatic temperature rise reaction was carried out. After about 30 minutes, 39 g of 1,3-butadiene was added to cap the end of the polymer with butadiene, and after about 10 minutes, N,N-diethyl-3-(trimethoxysilyl)propane-1- with a modifier An amine was added and reacted for 15 minutes ([DTP]:[act. Li]=1.5:1 molar ratio, [modifier]:[act. Li]=1:1 molar ratio). Then, the reaction was stopped using ethanol, and 33 g of a solution in which 30 wt% of an antioxidant, Wingstay K, was dissolved in hexane was added. The resulting polymer was put into hot water heated by steam, stirred to remove the solvent, and then roll-dried to remove the remaining solvent and water to prepare a modified styrene-butadiene copolymer.

Experimental Example 1

For each modified styrene-butadiene copolymer prepared in Examples and Comparative Examples, the styrene unit content and vinyl content in the polymer, the weight average molecular weight (Mw, X10 ³ g/mol), and the number average molecular weight (Mn, X10 ³ g) /mol), molecular weight distribution (PDI, MWD), Mooney viscosity (MV), Mooney viscosity change rate, and Si and N contents were respectively measured. The results are shown in Table 1 below.

1) Styrene units and vinyl content (wt%)

Styrene unit (SM) and vinyl (Vinyl) contents in each polymer were measured and analyzed using Varian VNMRS 500 MHz NMR.

For NMR measurement, 1,1,2,2-tetrachloroethane was used as the solvent, and the solvent peak was calculated as 5.97 ppm, 7.2~6.9 ppm is random styrene, 6.9~6.2 ppm is block styrene, and 5.8~5.1 ppm is 1,4-vinyl, 5.1-4.5 ppm was calculated as the peak of 1,2-vinyl, and the styrene unit and vinyl content were calculated.

2) Weight average molecular weight (Mw, X10) ³ g/mol), number average molecular weight (Mn, X10 ³ g/mol), molecular weight distribution (PDI, MWD)

The weight average molecular weight (Mw) and number average molecular weight (Mn) were measured through gel permeation chromatography (GPC) analysis, and a molecular weight distribution curve was obtained. In addition, molecular weight distributions (PDI, MWD, Mw/Mn) were calculated and obtained from each of the measured molecular weights. Specifically, the GPC uses a combination of two PLgel Olexis (Polymer Laboratories) columns and one PLgel mixed-C (Polymer Laboratories) column, and when calculating molecular weight, the GPC reference material (Standard material) is PS (polystyrene) was used. The GPC measurement solvent was prepared by mixing 2 wt% of an amine compound in tetrahydrofuran.

3) Mooney viscosity

The Mooney viscosity (MV, (ML1+4, @100°C) MU) was measured using MV-2000 (ALPHA Technologies) at 100°C at 100°C using a Rotor Speed of 2±0.02 rpm, a Large Rotor. After the sample was left at room temperature (23±3° C.) for more than 30 minutes, 27±3 g was collected, filled in the die cavity, and the platen was operated for measurement for 4 minutes.

4) Si content

The Si content was measured using an inductively coupled plasma emission analyzer (ICP-OES; Optima 7300DV) as an ICP analysis method. Specifically, about 0.7 g of the sample is placed in a platinum crucible (Pt crucible), and about 1 mL of concentrated sulfuric acid (98 wt%, Electronic grade) is added, heated at 300° C. for 3 hours, and the sample is heated in an electric furnace (Thermo Scientific, Lindberg Blue M), after conducting conversation with the program of steps 1 to 3 below,

1) step 1: initial temp 0℃, rate (temp/hr) 180 ℃/hr, temp(holdtime) 180℃ (1hr)

2) step 2: initial temp 180℃, rate (temp/hr) 85 ℃/hr, temp(holdtime) 370℃ (2hr)

3) step 3: initial temp 370℃, rate (temp/hr) 47 ℃/hr, temp(holdtime) 510℃ (3hr)

1 mL of concentrated nitric acid (48 wt%) and 20 μl of concentrated hydrofluoric acid (50 wt%) were added to the residue, sealed in a platinum crucible and shaken for at least 30 minutes, and then 1 mL of boric acid was added to the sample. and stored at 0° C. for 2 hours or more, diluted in 30 mL of ultrapure water, and measured by incineration.

5) N content

The N content was measured using a trace nitrogen quantitative analyzer (NSX-2100H) as an NSX analysis method. Specifically, turn on the trace nitrogen quantitative analyzer (Auto sampler, Horizontal furnace, PMT & Nitrogen detector), set the carrier gas flow rate to 250 ml/min for Ar, 350 ml/min for O ₂ , and 300 ml/min for the ozonizer, and heater was set to 800°C and then waited for about 3 hours to stabilize the analyzer. After the analyzer is stabilized, a calibration curve in the range of 5 ppm, 10 ppm, 50 ppm, 100 ppm and 500 ppm was prepared using Nitrogen standard (AccuStandard S-22750-01-5 ml), and the area corresponding to each concentration was obtained. Afterwards, a straight line was drawn using the ratio of concentration to area. Thereafter, a ceramic boat containing 20 mg of the sample was placed on the auto sampler of the analyzer and measured to obtain an area. The N content was calculated using the area of the obtained sample and the calibration curve.

division Example comparative example One 2 3 4 One 2 3 4 NMR
(weight%) SM 21 21 21 21 21 21 21 21 Vinyl 50 50 50 50 50 50 50 50 GPC Mn
(X10 ³ g/mol) 350 375 412 425 389 405 393 350 Mw
(X10 ³ g/mol) 472 525 680 722 447 514 491 490 PDI 1.35 1.40 1.65 1.70 1.15 1.27 1.25 1.40 Mooney viscosity (MV) 54 63 93 100 49 62 57 57 Si content (ppm) 79 72 157 162 215 78 80 185 N content (ppm) 375 377 375 362 213 39 375 316

As shown in Table 1, in Examples 1 to 4, the content of N atoms was significantly increased compared to Comparative Examples 1 and 2. In this case, Comparative Example 1 is a polymer prepared using the macromonomer presented in the present invention as a denaturation initiator and without using a denaturant, and Comparative Example 2 is a polymer prepared without using the macromonomer presented in the present invention. A second chain comprising a repeating unit derived from the compound represented by Formula 1 in the modified conjugated diene-based polymer according to the present invention from the fact that the N atom content in the polymers of Examples 1 to 4 was significantly increased compared to Comparative Examples 1 and 2; and a unit derived from an amine-containing alkoxysilane-based modifier.

In addition, in Example 1, the N content was greatly increased to about 19% compared to Comparative Example 4, and in Comparative Example 4, styrene and 1,3-butadiene and It is a polymer prepared without performing polymerization and reaction with a macromonomer after the denaturation reaction.

Through the above results, the modified conjugated diene-based polymer according to the present invention is prepared by a manufacturing method in which a macromonomer including a derived repeating unit represented by Formula 1 is reacted with a first chain which is an active polymer modified after the modification reaction As a result, it can be confirmed that N atoms in the polymer can be included in a higher content.

Experimental Example 2

In order to compare and analyze the physical properties of the rubber composition containing each modified styrene-butadiene copolymer prepared in Examples and Comparative Examples and molded articles prepared therefrom, tensile properties and viscoelastic properties were measured respectively, and the results are shown in Table 3 below shown in

1) Preparation of rubber specimens

Each of the modified or unmodified conjugated diene-based polymers of Examples, Comparative Examples and Reference Examples was used as a raw rubber and blended under the compounding conditions shown in Table 2 below. The content of the raw material in Table 2 is each part by weight based on 100 parts by weight of the raw rubber.

division Raw material Content (parts by weight) 1st stage kneading rubber 100 silica 70 Coupling agent (X50S) 11.2 fair oil 37.5 Zincizing agent 3 stearic acid 2 antioxidant 2 anti-aging agent 2 wax One 2nd stage kneading sulfur 1.5 rubber accelerator 1.75 vulcanization accelerator 2

Specifically, the rubber specimen is kneaded through the first stage kneading and the second stage kneading. In the first stage kneading, raw rubber, silica (filler), organosilane coupling agent (X50S, Evonik), process oil (TDAE oil), zincating agent (ZnO), stearic acid using a Banbari mixer with a temperature control device is used. , antioxidant (TMQ(RD) (2,2,4-trimethyl-1,2-dihydroquinoline polymer), antioxidant (6PPD ((dimethylbutyl)-N-phenyl-phenylenediamine) and wax (Microcrystaline Wax) ) was kneaded.At this time, the initial temperature of the kneader was controlled to 70° C., and after the mixing was completed, a first formulation was obtained at a discharge temperature of 145° C. to 155° C. In the second stage of kneading, the first formulation was cooled to room temperature. After that, the primary compound, sulfur, rubber accelerator (DPG (diphenylguanidine)) and vulcanization accelerator (CZ (N-cyclohexyl-2-benzothiazylsulfenamide)) are added to the kneader, and at a temperature of 100° C. or less A secondary compound was obtained by mixing, and then, a rubber specimen was prepared through a curing process at 160° C. for 20 minutes.

2) Tensile properties

For tensile properties, each test piece was prepared according to the tensile test method of ASTM 412, and the tensile stress (300% modulus) at 300% elongation of the test piece was measured. Specifically, the tensile properties were measured at room temperature at a speed of 50 cm/min using a Universal Test Machin 4204 (Instron Co., Ltd.) tensile tester.

3) Viscoelastic properties

For the viscoelastic properties, the tan δ value was confirmed by measuring the viscoelastic behavior against dynamic deformation at a frequency of 10 Hz and each measurement temperature (-60°C to 60°C) in Film Tension mode using a dynamic mechanical analyzer (GABO). In the measurement result, the higher the low temperature 0℃ tan δ value, the better the wet road resistance, and the lower the high temperature 60℃ tan δ value, the less the hysteresis loss and the better the rolling resistance (fuel efficiency). Since the result value is expressed in Index (%) based on the result value of Comparative Example 1, the higher the numerical value, the better.

4) Machinability characteristics

1) The Mooney viscosity (MV, (ML1+4, @100℃) MU) of the primary compound obtained during the manufacture of 1) rubber specimen was measured to compare and analyze the processability characteristics of each polymer. In this case, the lower the Mooney viscosity measurement value, the more This indicates that the workability characteristics are excellent, and in Table 3 below, it is expressed as an Index (%) based on the result value of Comparative Example 2, and the higher the number, the better.

Specifically, using MV-2000 (ALPHA Technologies) at 100°C, using a Rotor Speed of 2±0.02 rpm, and a Large Rotor, each primary formulation was left at room temperature (23±3°C) for at least 30 minutes and then 27 ±3 g was collected and filled inside the die cavity, and the platen was operated for 4 minutes.

division Example comparative example One 2 3 4 One 2 3 4 300% modulus (Index) 162 160 161 165 148 149 162 165 viscoelastic
characteristic tan δ
(at 0℃ Index) 101 99 97 101 100 97 98 98 tan δ
(at 60℃ Index) 121 122 119 118 100 97 120 123 Machinability characteristics (Index) 101 100 104 105 89 100 74 60

As shown in Table 3, the modified styrene-butadiene copolymers of Examples 1 to 4, which were reacted with a macromonomer after the modification reaction using the modifier according to an embodiment of the present invention, showed superior processability characteristics compared to Comparative Examples 1 to 3 It was confirmed that the tensile properties and viscoelastic properties were also excellent at the same time.

In particular, Example 1 exhibited significantly improved processability characteristics while exhibiting equally excellent tensile properties and viscoelastic properties compared to Comparative Example 3, wherein Comparative Example 3 uses the macromonomer in Example 1 as a modification initiator, and the modification reaction It is a modified styrene-butadiene copolymer prepared in the same manner as in Example 1, except that the step of reacting with the macromonomer was not performed thereafter.

Although the difference in the manufacturing method of Example 1 and Comparative Example 3 and the Si atoms and N atoms in the polymer are contained at the same level as in Example 1, the present invention is modified through the significant difference in effect between Example 1 and Comparative Example 3 The conjugated diene-based polymer is a copolymer having a structure different from that of Comparative Example 3, for example, a second chain containing a repeating unit derived from a compound represented by Formula 1 derived from a macromonomer is modified in the first chain by a modifier-derived unit. It can be predicted that the coupling is coupled to the same structure as the graft copolymer, and it was confirmed that the tensile properties, viscoelastic properties, and processability properties had a remarkably excellent effect in a balanced manner due to this structural difference (Table 1 and Table 3 above) Reference).

In addition, through Table 1 and Table 3, the modified conjugated diene-based polymer of the present invention is prepared by a manufacturing method comprising the step of reacting with a macromonomer after the modification reaction, thereby the compound represented by Formula 1 as in Comparative Example 4 It can be confirmed that N atoms in the polymer may be present in a high content compared to the polymer prepared by applying as a modified monomer, thereby exhibiting a remarkable effect that is not expressed in the polymer as in Comparative Example 4.

Claims (13)

a first chain comprising a repeating unit derived from a conjugated diene-based monomer; a second chain comprising a repeating unit derived from a compound represented by the following formula (1); and a unit derived from an amine-containing alkoxysilane-based modifier,
A modified conjugated diene-based polymer in which the first chain and the second chain are coupled by a modifier-derived unit:
[Formula 1]

In Formula 1,
R _1a to R _1c are each independently a hydrogen atom; an alkyl group having 1 to 20 carbon atoms; an alkenyl group having 2 to 20 carbon atoms; an alkynyl group having 2 to 20 carbon atoms; A heteroalkyl group having 1 to 20 carbon atoms, a heteroalkenyl group having 2 to 20 carbon atoms; a heteroalkynyl group having 2 to 20 carbon atoms; a cycloalkyl group having 5 to 20 carbon atoms; an aryl group having 6 to 20 carbon atoms; Or a heterocyclic group having 3 to 20 carbon atoms,
R _1d is a single bond, an alkylene group having 1 to 20 carbon atoms that is unsubstituted or substituted with a substituent; a cycloalkylene group having 5 to 20 carbon atoms that is unsubstituted or substituted with a substituent; Or an arylene group having 6 to 20 carbon atoms substituted or unsubstituted with a substituent, wherein the substituent is an alkyl group having 1 to 10 carbon atoms, a cycloalkyl group having 5 to 10 carbon atoms, or an aryl group having 6 to 20 carbon atoms,
R _1f and R _1g are each independently a single bond, an alkylene group having 1 to 20 carbon atoms substituted or unsubstituted with a substituent; a cycloalkylene group having 5 to 20 carbon atoms that is unsubstituted or substituted with a substituent; Or an arylene group having 6 to 20 carbon atoms substituted or unsubstituted with a substituent, wherein the substituent is an alkyl group having 1 to 10 carbon atoms, a cycloalkyl group having 5 to 10 carbon atoms, or an aryl group having 6 to 20 carbon atoms,
R _1h, R _1i, R _1j and R _1k are each independently an alkyl group having 1 to 20 carbon atoms; an alkenyl group having 2 to 20 carbon atoms; an alkynyl group having 2 to 20 carbon atoms; a heteroalkyl group having 1 to 20 carbon atoms; a heteroalkenyl group having 2 to 20 carbon atoms; a heteroalkynyl group having 2 to 20 carbon atoms; a cycloalkyl group having 5 to 20 carbon atoms; an aryl group having 6 to 20 carbon atoms; or a heterocyclic group having 3 to 20 carbon atoms.
According to claim 1,
In Formula 1,
R _1a to R _1c are each independently a hydrogen atom; an alkyl group having 1 to 10 carbon atoms; an alkenyl group having 2 to 10 carbon atoms; an alkynyl group having 2 to 10 carbon atoms; A heteroalkyl group having 1 to 10 carbon atoms, a heteroalkenyl group having 2 to 10 carbon atoms; a heteroalkynyl group having 2 to 10 carbon atoms; a cycloalkyl group having 5 to 10 carbon atoms; an aryl group having 6 to 12 carbon atoms; Or a heterocyclic group having 3 to 10 carbon atoms,
R _1d is a single bond or an unsubstituted alkylene group having 1 to 10 carbon atoms, R _1f and R _1g are each independently a single bond or an unsubstituted alkylene group having 1 to 10 carbon atoms,
R _1h, R _1i, R _1j and R _1k are each independently an alkyl group having 1 to 10 carbon atoms; an alkenyl group having 2 to 10 carbon atoms; an alkynyl group having 2 to 10 carbon atoms; a heteroalkyl group having 1 to 10 carbon atoms; a heteroalkenyl group having 2 to 10 carbon atoms; a heteroalkynyl group having 2 to 10 carbon atoms; a cycloalkyl group having 5 to 10 carbon atoms; an aryl group having 6 to 12 carbon atoms; Or a modified conjugated diene-based polymer that is a heterocyclic group having 3 to 10 carbon atoms.
According to claim 1,
In Formula 1,
R _1a to R _1c are each independently a hydrogen atom; or having 1 to 10 carbon atoms, R _1d is a single bond or an unsubstituted C 1 to C 6 alkylene group, R _1f and R _1g are each independently a single bond or an unsubstituted C 1 to C 6 alkylene group, R _1h, R _1i, R _1j and R _1k are each independently an alkyl group having 1 to 10 carbon atoms.
According to claim 1,
The first chain is a modified conjugated diene-based polymer further comprising a repeating unit derived from an aromatic vinyl-based monomer.
According to claim 1,
The second chain is a modified conjugated diene-based polymer further comprising a unit derived from a conjugated diene-based monomer.
According to claim 1,
a number average molecular weight (Mn) of 1,000 g/mol to 2,000,000 g/mol, a weight average molecular weight (Mw) of 1,000 g/mol to 3,000,000 g/mol, and a peak average molecular weight (Mp) of 1,000 g/mol to 3,000,000 g /mol of a modified conjugated diene-based polymer.
preparing an active first chain by polymerizing a conjugated diene-based monomer or a conjugated diene-based monomer or an aromatic vinyl-based monomer in a carbon solvent in the presence of a polymerization initiator (S1);
preparing a modified active first chain by reacting the active first chain with an amine-containing alkoxysilane-based modifier (S2); and
A method for producing the modified conjugated diene-based polymer of claim 1, comprising the step (S3) of reacting the modified active first chain with a macromonomer including a repeating unit derived from a compound represented by the following formula (1):
[Formula 1]

In Formula 1,
R _1a to R _1c are each independently a hydrogen atom; an alkyl group having 1 to 20 carbon atoms; an alkenyl group having 2 to 20 carbon atoms; an alkynyl group having 2 to 20 carbon atoms; A heteroalkyl group having 1 to 20 carbon atoms, a heteroalkenyl group having 2 to 20 carbon atoms; a heteroalkynyl group having 2 to 20 carbon atoms; a cycloalkyl group having 5 to 20 carbon atoms; an aryl group having 6 to 20 carbon atoms; Or a heterocyclic group having 3 to 20 carbon atoms,
R _1d is a single bond, an alkylene group having 1 to 20 carbon atoms that is unsubstituted or substituted with a substituent; a cycloalkylene group having 5 to 20 carbon atoms that is unsubstituted or substituted with a substituent; Or an arylene group having 6 to 20 carbon atoms substituted or unsubstituted with a substituent, wherein the substituent is an alkyl group having 1 to 10 carbon atoms, a cycloalkyl group having 5 to 10 carbon atoms, or an aryl group having 6 to 20 carbon atoms,
R _1f and R _1g are each independently a single bond, an alkylene group having 1 to 20 carbon atoms substituted or unsubstituted with a substituent; a cycloalkylene group having 5 to 20 carbon atoms that is unsubstituted or substituted with a substituent; Or an arylene group having 6 to 20 carbon atoms substituted or unsubstituted with a substituent, wherein the substituent is an alkyl group having 1 to 10 carbon atoms, a cycloalkyl group having 5 to 10 carbon atoms, or an aryl group having 6 to 20 carbon atoms,
R _1h, R _1i, R _1j and R _1k are each independently an alkyl group having 1 to 20 carbon atoms; an alkenyl group having 2 to 20 carbon atoms; an alkynyl group having 2 to 20 carbon atoms; a heteroalkyl group having 1 to 20 carbon atoms; a heteroalkenyl group having 2 to 20 carbon atoms; a heteroalkynyl group having 2 to 20 carbon atoms; a cycloalkyl group having 5 to 20 carbon atoms; an aryl group having 6 to 20 carbon atoms; or a heterocyclic group having 3 to 20 carbon atoms.
8. The method of claim 7,
The macromonomer is a method for producing a modified conjugated diene-based polymer further comprising a unit derived from a conjugated diene-based monomer,
8. The method of claim 7,
The macromonomer is a compound represented by Formula 1 in the presence of an organolithium compound in a hydrocarbon solvent; Or a method for producing a modified conjugated diene-based polymer prepared by low-polymerization reaction of the compound represented by Formula 1 and the conjugated diene-based monomer.
8. The method of claim 7,
The method for producing a modified conjugated diene-based polymer, wherein the modifier is used in an amount of 0.1 to 10 moles relative to 1 mole of the polymerization initiator.
8. The method of claim 7,
The method for producing a modified conjugated diene-based polymer wherein the macromonomer is used in an amount of 0.1 to 4.0 moles relative to 1 mole of the polymerization initiator.
A rubber composition comprising the modified conjugated diene-based polymer of claim 1 and a filler.
13. The method of claim 12,
A rubber composition comprising 0.1 parts by weight to 200 parts by weight of a filler based on 100 parts by weight of the modified conjugated diene-based polymer.