KR102438613B1 - Polyester composite using solid dispersion of anhydrosugar alcohol and method for preparing the same, and molded article comprising the same - Google Patents

Abstract

The present invention relates to a polyester composite, a method for manufacturing the same, and a molded article including the same, and more specifically, to a polyester resin in which anhydrosugar alcohol is copolymerized, including a matrix resin and a nanomaterial dispersed in the matrix resin By using a solid dispersion obtained by introducing a nanomaterial (disperse) into anhydrosugar alcohol (dispersion medium) in an aqueous dispersion state and a specific aliphatic diol compound as a diol component, the existing polyester resin Polyester composite and its manufacturing method, which exhibits significantly improved mechanical properties than the composite (for example, tensile strength, tensile modulus and elongation, etc.), and has uniform physical properties because the nanomaterial is uniformly dispersed in the composite; And it relates to a molded article comprising the same.

Description

Polyester composite using solid dispersion of anhydrosugar alcohol and manufacturing method thereof, and molded article comprising the same, and molded article comprising the same

The present invention relates to a polyester composite, a method for manufacturing the same, and a molded article including the same, and more specifically, to a polyester resin in which anhydrosugar alcohol is copolymerized, including a matrix resin and a nanomaterial dispersed in the matrix resin By using a solid dispersion obtained by introducing a nanomaterial (disperse) into anhydrosugar alcohol (dispersion medium) in an aqueous dispersion state and a specific aliphatic diol compound as a diol component, the existing polyester resin Polyester composite and its manufacturing method, which exhibit significantly improved mechanical properties than the composite (for example, tensile strength, tensile modulus and elongation, etc.), and have uniform properties because the nanomaterial is uniformly dispersed in the composite; And it relates to a molded article comprising the same.

Nanomaterials such as nanocellulose can be manufactured from biomass through various methods, and recently, many studies have been conducted to improve mechanical properties by adding it to polyurethane. However, due to the hydrophilicity of nanocellulose, most of the products are manufactured using water as a dispersion medium in an amount of about 1% by weight, so there is a limit to its application when manufacturing a composite material with a polymer resin.

In addition, when nano-cellulose is directly used in the form of solid crystals or powder without dispersing it in water, aggregation occurs between the nano-celluloses, and the physical properties of the polymer resin composite material produced therefrom are reduced. It has the disadvantage of becoming non-uniform.

Therefore, as a resin composite including a matrix resin and a nanomaterial dispersed therein, the nanomaterial is uniformly dispersed in the matrix resin while containing the nanomaterial in a higher content than in the prior art, so that physical properties (especially in comparison to the existing resin composite) , tensile strength, tensile modulus, elongation, etc.) is being requested to develop a resin composite with significantly improved properties.

An object of the present invention is to exhibit significantly improved mechanical properties (for example, tensile strength, tensile modulus, and elongation, etc.) compared to the existing polyester resin composite, and the nanomaterial is uniformly dispersed in the composite, resulting in uniform physical properties. To provide an ester complex, a method for manufacturing the same, and a molded article including the same.

In order to solve the above technical problem, the present invention includes a matrix resin and a nanomaterial dispersed in the matrix resin, wherein the matrix resin is a solid dispersion of anhydrosugar alcohol in which the nanomaterial is dispersed therein; and a polyester resin that is a polymerization reaction product of a diol component and a dicarboxyl component comprising an aliphatic diol compound selected from ethylene glycol, butanediol, cyclohexanedimethanol, or a mixture thereof, wherein the solid dispersion of the anhydrosugar alcohol is It provides a polyester composite, which is obtained by introducing the nanomaterial into anhydrosugar alcohol in an aqueous dispersion state.

According to another aspect of the present invention, the nanomaterial is a solid dispersion of anhydrosugar alcohol dispersed therein, and a diol component comprising an aliphatic diol compound selected from ethylene glycol, butanediol, cyclohexanedimethanol, or a mixture thereof and a polymerization reaction of the dicarboxyl component, wherein the solid dispersion of the anhydrosugar alcohol is obtained by introducing the nanomaterial into the anhydrosugar alcohol in an aqueous dispersion state, a method for producing a polyester composite is provided .

According to another aspect of the present invention, there is provided a molded article comprising the polyester composite of the present invention.

The polyester composite according to the present invention, compared to the existing polyester resin composite, in particular, the nano material (eg, nano cellulose, etc.) is directly used in the form of a solid crystal or powder without dispersing in water, compared to the resin composite , mechanical properties (eg, tensile strength, tensile modulus, elongation, etc.), and the nanomaterial is uniformly dispersed in the composite to have uniform physical properties.

Hereinafter, the present invention will be described in more detail.

The polyester composite of the present invention includes a matrix resin and a nanomaterial dispersed in the matrix resin.

In the present invention, the "nano material" refers to an organic or inorganic material having a size (length or particle diameter) of sub-microns, that is, less than 1 micrometer (eg, 10-900 nm, or 10-500 nm). do.

As such a nanomaterial, a material satisfying the meaning of the above-mentioned nanomaterial, for example, nanocellulose, carbon nanofiber, carbon nanotube, iron, aluminum, chromium, nickel, cobalt, zinc, tungsten, indium, tin, palladium , zirconium, titanium, copper, silver, gold, platinum, kaolin, clay, talc, mica, silica, bentonite, dolomite, calcium silicate, magnesium silicate, asbestos, calcium carbonate, magnesium carbonate, barium carbonate, calcium sulfate, barium sulfate, Aluminum sulfate, aluminum hydroxide, iron hydroxide, aluminum silicate, zirconium oxide, magnesium oxide, aluminum oxide, titanium oxide, iron oxide, zinc oxide, antimony trioxide, indium oxide, indium tin oxide, silicon carbide, silicon nitride, boron nitride, barium titanate, diatomaceous earth , carbon black, rock wool, graphene, graphite, graphene oxide, azo compound, diazo compound, condensed azo compound, thioindigo compound, indanthrone compound, quinacrindone compound, anthraquinone compound, benzimi Dazolone-based compound, perylene-based compound, phthalocyanine-based compound, anthrapyridine-based compound, dioxazine-based compound, polyethylene resin, polypropylene resin, polyester resin, nylon resin, polyamide resin, aramid resin, urethane resin, polystyrene resin, poly One selected from lactic acid, cellulose acetate fiber, hemicellulose, lignin, chitin, chitosan, starch, or mixtures thereof may be used.

In one embodiment, the nanomaterial may be selected from nanocellulose, carbon nanofibers, carbon nanotubes, or a mixture thereof, but is not limited thereto.

In one embodiment, the nano-cellulose may be selected from nano-cellulose fibers, nano-cellulose crystals, or mixtures thereof.

In one embodiment, the carbon nanotubes may be selected from single-walled carbon nanotubes, multi-walled carbon nanotubes, or mixtures thereof.

In one embodiment, the content of the nanomaterial in the polyester composite of the present invention, based on the total weight of the composite, 0.1 wt% or more, 0.2 wt% or more, 0.3 wt% or more, 0.4 wt% or more, or 0.45 wt% or more, and may also be 10 wt% or less, 9 wt% or less, 8 wt% or less, 7 wt% or less, 5 wt% or less, 4 wt% or less, 3 wt% or less, 2.5 wt% or less, or 2 wt% or less and, for example, may be 0.1 wt% to 10 wt%, more specifically 0.1 wt% to 5 wt%, and even more specifically 0.1 wt% to 3 wt%. If the content of the nanomaterial in the composite is lower than the above level, the improvement effect of mechanical strength such as tensile strength of the composite may be insignificant. , it may be difficult to obtain a polymer composite having uniform physical properties.

The matrix resin included in the polyester composite of the present invention is a solid dispersion of anhydrosugar alcohol in which the nanomaterial is dispersed, and an aliphatic diol selected from ethylene glycol, butanediol, cyclohexanedimethanol, or a mixture thereof It is a polyester resin that is a polymerization reaction product of a diol component and a dicarboxyl component containing a compound, and the solid dispersion of the anhydrosugar alcohol is obtained by introducing the nanomaterial in an aqueous dispersion state into anhydrosugar alcohol.

Anhydrosugar alcohol can be prepared by dehydrating a hydrogenated sugar derived from a natural product. Hydrogenated sugar (also referred to as “sugar alcohol”) refers to a compound obtained by adding hydrogen to a reducing end group of a saccharide, generally HOCH ₂ (CHOH) _n CH ₂ OH (where n is an integer of 2 to 5) ), and is classified into tetritol, pentitol, hexitol, and heptitol (with 4, 5, 6 and 7 carbon atoms, respectively) according to the number of carbon atoms. Among them, hexitol having 6 carbon atoms includes sorbitol, mannitol, iditol, galactitol, and the like, and sorbitol and mannitol are particularly effective substances.

In the present invention, the anhydrosugar alcohol may be mono-anhydrosugar alcohol, dianhydrosugar alcohol, or a mixture thereof, which is anhydrosugar by dehydrating hydrogenated sugar (eg, hexitol such as sorbitol, mannitol, iditol). It can be obtained in the process of preparing alcohol.

The monoanhydrosugar alcohol is an anhydrosugar alcohol formed by removing one water molecule from the inside of a hydrogenated sugar, and has a tetraol form having four hydroxyl groups in the molecule. The type of mono-anhydrosugar alcohol that can be used in the present invention is not particularly limited, but may preferably be mono-anhydrosugar hexitol, and more specifically, 1,4-anhydrohexitol, 3,6-anhydrohexitol, 2,5-anhydrohexitol, 1,5-anhydrohexitol, 2,6-anhydrohexitol, or a mixture of two or more thereof.

The dianhydrosugar alcohol is an anhydrosugar alcohol formed by removing two water molecules from the inside of a hydrogenated sugar, has a diol form with two hydroxyl groups in the molecule, and can be prepared using hexitol derived from starch. . Since dianhydrosugar alcohol is an eco-friendly material derived from renewable natural resources, research on its manufacturing method has been conducted with a lot of interest from a long time ago. Among these dianhydrosugar alcohols, isosorbide prepared from sorbitol has the widest industrial application range at present. The type of dianhydrosugar alcohol that can be used in the present invention is not particularly limited, but may preferably be dianhydrosugar hexitol, and more specifically 1,4-3,6-dianhydrohexitol. The 1,4-3,6-dianhydrohexitol may be isosorbide, isomannide, isoidide, or a mixture of two or more thereof, more preferably isosorbide.

In one embodiment, the solid dispersion of the anhydrosugar alcohol is added to the anhydrosugar alcohol in an aqueous dispersion state of the nanomaterial (eg, a state in which the nanomaterial is dispersed in water at a concentration of 0.1 to 5% by weight) and uniformly It is a room temperature solid dispersion obtained by mixing and melting while removing moisture by applying a vacuum at a temperature higher than the melting point of anhydrosugar alcohol (for example, a temperature of 80° C. or higher), and then cooling the molten mixture to room temperature.

In one embodiment, the content of the nanomaterial introduced into the solid dispersion of the anhydrosugar alcohol is, based on the total weight of the solid dispersion, 0.2 wt% or more, 0.3 wt% or more, 0.4 wt% or more, 0.5 wt% % or more, 0.6 wt% or more, 0.7 wt% or more, 0.8 wt% or more, 0.9 wt% or more, or 1 wt% or more, and also 15 wt% or less, 14 wt% or less, 13 wt% or less, 12 wt% or less , may be 11 wt% or less or 10 wt% or less, for example, 0.2 wt% to 15 wt%, more specifically 0.5 wt% to 12 wt%, even more specifically 1 wt% % to 10% by weight.

The matrix resin included in the polyester composite of the present invention is a solid dispersion of such anhydrosugar alcohol, and a diol component comprising an aliphatic diol compound selected from ethylene glycol, butanediol, cyclohexanedimethanol, or a mixture thereof and a diol It is a polyester resin which is a polymerization reaction product of a carboxyl component.

The butane diol may be selected from 1,2-butane diol, 1,3-butane diol, 1,4-butane diol, or a combination thereof.

The cyclohexane dimethanol may be selected from 1,2-cyclohexane dimethanol, 1,3-cyclohexane dimethanol, 1,4-cyclohexane dimethanol, or a combination thereof.

In one embodiment, the dicarboxyl component may be selected from an aliphatic dicarboxyl compound, an aromatic dicarboxyl compound, or a combination thereof, and may preferably include an aromatic dicarboxyl compound.

In one embodiment, the aliphatic dicarboxyl compound may be selected from aliphatic dicarboxylic acids having 4 to 14 carbon atoms or esters thereof.

More specifically, the aliphatic dicarboxyl compound is adipic acid or its ester, cyclohexanedicarboxylic acid or its ester, sebacic acid or its ester, isodecylsuccinic acid or its ester, maleic acid or its ester, fumaric acid or its ester ester, succinic acid or its ester, glutaric acid or its ester, azelaic acid or its ester, itaconic acid or its ester, glutamic acid or its ester, 2,5-furandicarboxylic acid or its ester, tetrahydrofuran-2, 5-dicarboxylic acid or its ester, tetrahydrofuran-3,5-dicarboxylic acid or its ester, undecanedioic acid or its ester, dodecanedioic acid or its ester, tridecanedioic acid or its ester, tetradecanedioic acid Or it may be selected from the group consisting of esters thereof, and combinations thereof. The ester compound of the aliphatic dicarboxylic acid may be a monoester compound, a diester compound, or a mixture thereof, and more specifically, a diester compound. For example, the diester compound of the aliphatic dicarboxylic acid may be dimethyl adipate, diethyl adipate, dimethyl succinate or diethyl succinate. More specifically, the aliphatic dicarboxyl compound may include adipic acid or an ester thereof.

In one embodiment, the aromatic dicarboxyl compound may be selected from aromatic dicarboxylic acids having 8 to 16 carbon atoms or esters thereof.

More specifically, the aromatic dicarboxylic compound is phthalic acid or an acid anhydride or ester thereof, terephthalic acid or an acid anhydride or ester thereof, isophthalic acid or an acid anhydride or ester thereof, 1,5-naphthalenedicarboxylic acid or an acid anhydride thereof, or ester, 2,6-naphthalenedicarboxylic acid or its acid anhydride or ester, 2,5-furandicarboxylic acid or its acid anhydride or ester, diphenic acid or its acid anhydride or ester, p-phenylene diacetic acid or It may be selected from the group consisting of an acid anhydride or ester thereof, o-phenylene diacetic acid or an acid anhydride or ester thereof, and combinations thereof. The ester compound of the aromatic dicarboxylic acid may be a monoester compound, a diester compound, or a mixture thereof, and more specifically, a diester compound. For example, the ester compound of the aromatic dicarboxylic acid is dimethyl terephthalate, diethyl terephthalate, dimethyl isophthalate, diethyl isophthalate, dimethyl 2,5-furandicarboxylate or diethyl 2,5- It may be furandicarboxylate or the like.

In one embodiment, the diol component, in addition to the solid dispersion of the anhydrosugar alcohol, and an aliphatic diol compound selected from ethylene glycol, butane diol, cyclohexanedimethanol, or mixtures thereof, may further include an additional diol component. can

In one embodiment, the additional diol component may be a diol component represented by the following Chemical Formula 1:

[Formula 1]

In Formula 1, X is a mononuclear or polynuclear arylene group having 6 to 30 carbon atoms; a linear alkylene group having 1 to 15 carbon atoms; a branched alkylene group having 3 to 15 carbon atoms; or a cyclic alkylene group having 3 to 15 carbon atoms, wherein the arylene group, linear alkylene group, branched alkylene group and cyclic alkylene group are each a halogen atom, an alkyl group, a cycloalkyl group, an alkenyl group, an alkoxy group, an aryl group, a nitro group, or It may be substituted or unsubstituted with a carboxyl group, with the proviso that ethylene glycol, butane diol, and cyclohexanedimethanol are excluded from the diol component represented by Formula (1).

In one embodiment, in Formula 1, the halogen atom may be F, Cl or Br, and the alkyl group is an alkyl group having 1 to 20 carbon atoms (more specifically, an alkyl group having 1 to 13 carbon atoms, for example, methyl, ethyl , propyl or butyl), and the cycloalkyl group may be a cycloalkyl group having 3 to 10 carbon atoms (more specifically, a cycloalkyl group having 3 to 6 carbon atoms), and the alkenyl group is an alkenyl group having 2 to 20 carbon atoms (more Specifically, it may be an alkenyl group having 2 to 13 carbon atoms), and the alkoxy group is an alkoxy group having 1 to 20 carbon atoms (more specifically, an alkoxy group having 1 to 13 carbon atoms, for example, methoxy, ethoxy, propoxy or butoxy), and the aryl group may be an aryl group having 6 to 30 carbon atoms (more specifically, an aryl group having 6 to 20 carbon atoms, for example, a phenyl group, tolyl group, xylenyl group, or naphthyl group). However, ethylene glycol, butane diol, and cyclohexanedimethanol are excluded from the diol component represented by the formula (1).

In one embodiment, in Formula 1, X is a substituted or unsubstituted bisphenol (eg, bisphenol A, bisphenol F or bisphenol TMC, etc.), a substituted or unsubstituted resorcinol, a substituted or unsubstituted hydroquinone (eg, For example, hydroquinone, 2-nitro hydroquinone, 2-sulfonyl hydroquinone, etc.), substituted or unsubstituted biphenol, substituted or unsubstituted naphthalenediol, or arylene which may be derived from substituted or unsubstituted diphenylphenol It may be a group, for example, it may be represented by the following formulas 1a to 1h.

[Formula 1a]

[Formula 1b]

[Formula 1c]

[Formula 1d]

[Formula 1e]

[Formula 1f]

[Formula 1g]

[Formula 1h]

In one embodiment, in Formula 1, X may be an alkylene group that may be derived from a substituted or unsubstituted propylene glycol, for example, a propylene group.

In one embodiment, in Formula 1, X may be a cycloalkylene group that may be derived from a substituted or unsubstituted cyclohexane diol, or a substituted or unsubstituted tetramethylcyclobutane diol, for example, in Formula 1i and 1j.

[Formula 1i]

[Formula 1j]

In one embodiment, the diol component represented by Formula 1 may be an aromatic diol, an aliphatic diol other than ethylene glycol and butane diol, an alicyclic diol other than anhydrosugar alcohol and cyclohexanedimethanol, or a mixture thereof.

Examples of the aromatic diol include bisphenol (eg, bisphenol A, bisphenol F, bisphenol which is unsubstituted or substituted with a halogen atom, an alkyl group, a cycloalkyl group, an alkenyl group, an alkoxy group, an aryl group, a nitro group or a carboxyl group). TMC, etc.), resorcinol, hydroquinone, biphenol, naphthalene diol, or a mixture thereof may be used, preferably substituted with a halogen atom, an alkyl group, a cycloalkyl group, an alkenyl group, an alkoxy group, an aryl group, a nitro group or a carboxyl group Bisphenol A, optionally or unsubstituted, may be used.

Examples of the aliphatic diol include, for example, a halogen atom, an alkyl group, a cycloalkyl group, an alkenyl group, an alkoxy group, an aryl group, a nitro group or a carboxyl group, unsubstituted or substituted with 2 to 15 carbon atoms, more specifically 2 to 10 carbon atoms may be an aliphatic diol other than ethylene glycol and butanediol of ,2-pentanediol, 1,3-pentanediol, 1,4-pentanediol and 1,5-pentanediol, etc.), hexanediol (1,2-hexanediol, 1,3-hexanediol, 1,4- hexanediol, 1,5-hexanediol and 1,6-hexanediol, etc.), neopentyl glycol, 2,2-dimethyl-1,3-propanediol, 2-ethyl-2-t-butyl-1,3- propane diol, 2,2,4-trimethyl-1,6-hexane diol, or mixtures thereof.

As the alicyclic diol other than the anhydrosugar alcohol and cyclohexanedimethanol, for example, cyclohexane unsubstituted or substituted with a halogen atom, an alkyl group, a cycloalkyl group, an alkenyl group, an alkoxy group, an aryl group, a nitro group or a carboxyl group. diol (1,2-cyclohexane diol, 1,3-cyclohexane diol and 1,4-cyclohexane diol, etc.), tetramethylcyclobutane diol, tricyclodecanedimethanol, adamantanediol, or mixtures thereof have.

In one embodiment, the content of the dicarboxyl component included as a repeating unit in the polyester resin is, based on 100% by weight of the total repeating units in the resin, 30% by weight or more, 35% by weight or more, 40% by weight or more, 45 weight % or more, 50 wt% or more, 60 wt% or more, or 63 wt% or more, and 80 wt% or less, 79 wt% or less, 78 wt% or less, 77 wt% or less, 76 wt% or less, 75 wt% or less or 74% by weight or less, for example 30 to 80% by weight, 40 to 78% by weight, 50 to 76% by weight or 60 to 75% by weight.

In one embodiment, the content of anhydrosugar alcohol included as a repeating unit in the polyester resin is 1 wt% or more, 2 wt% or more, 3 wt% or more, 4 wt%, based on 100 wt% of the total repeating units in the resin. % or more or 5 wt% or more, and 30 wt% or less, 29 wt% or less, 28 wt% or less, 27 wt% or less, 26 wt% or less, 25 wt% or less, 23 wt% or less, 21 wt% or less, or 20% by weight or less, for example 1 to 30% by weight, 3 to 28% by weight, 5 to 25% by weight or 5 to 20% by weight.

In one embodiment, the content of the aliphatic diol compound selected from ethylene glycol, butane diol, cyclohexanedimethanol, or a mixture thereof included as a repeating unit in the polyester resin is 100% by weight of the total repeating unit in the resin. , 1 wt% or more, 2 wt% or more, 3 wt% or more, 4 wt% or more, 5 wt% or more, 10 wt% or more, or 13 wt% or more, and 35 wt% or less, 34 wt% or less, 33 wt% or more % or less, 32 wt% or less, 31 wt% or less, 30 wt% or less, 29 wt% or less or 28 wt% or less, for example 1-35 wt%, 3-33 wt%, 5-30 wt% or 10 to 30% by weight.

In one embodiment, the intrinsic viscosity (IV) of the polyester composite may be 0.6 or more, 0.65 or more, or 0.7 or more, and may be less than 1.3, 1.25 or less, or 1.2 or less. The intrinsic viscosity (IV) can be measured at 35° C. by dissolving the polyester composite in a mixture of phenol and tetrachloroethane (weight ratio = 50:50) to prepare a 0.5 wt% solution, and then using an Uberod viscometer. .

In one embodiment, the reaction molar ratio of the diol component to the dicarboxyl component (the total number of moles of the diol component/the total number of moles of the dicarboxyl component) may be 1 to 1.5. If the reaction molar ratio is less than 1, the unreacted dicarboxyl component remains during the polymerization reaction and there is a risk that the mechanical properties and color of the polyester composite may decrease, and if it exceeds 1.5, the polymerization reaction rate is too slow and the productivity of the polyester composite There is a possibility that this may decrease.

The polyester composite according to the present invention, compared to the existing polyester resin composite, in particular, the nano material (eg, nano cellulose, etc.) is directly used in the form of a solid crystal or powder without dispersing in water, compared to the resin composite , exhibits significantly improved mechanical properties (eg, tensile strength, tensile modulus and elongation, etc.), and the nanomaterial is uniformly dispersed in the composite to have uniform physical properties.

In one embodiment, when the aliphatic diol compound is ethylene glycol, the polyester composite of the present invention may exhibit a tensile strength of 48 MPa or more, specifically 50 MPa or more, and more specifically 51 MPa or more.

In one embodiment, when the aliphatic diol compound is butane diol, the polyester composite of the present invention may exhibit a tensile strength of 109 MPa or more, specifically 110 MPa or more.

In one embodiment, when the aliphatic diol compound is a mixture of ethylene glycol and cyclohexanedimethanol, the polyester composite of the present invention has a tensile strength of 31 MPa or more, specifically 32 MPa or more, more specifically 34 MPa. can indicate

The tensile strength may be, for example, a value measured using a universal testing machine (UTM) based on ASTM D638.

In addition, the polyester composite according to the present invention, since the nanomaterial is uniformly dispersed in the matrix resin, it is possible to uniformly maintain physical properties (in particular, tensile strength, tensile modulus and elongation, etc.) compared to the existing resin composite.

In one embodiment, when the aliphatic diol compound is ethylene glycol, the polyester composite of the present invention may exhibit a standard deviation of tensile strength of 4.5 MPa or less.

More specifically, when the aliphatic diol compound is ethylene glycol, the standard deviation of the tensile strength may be 4.0 MPa or less, 3.0 MPa or less, 2.5 MPa or less, 2.0 MPa or less, 1.9 MPa or less, or 1.8 MPa or less.

In one embodiment, when the aliphatic diol compound is butane diol, the polyester composite of the present invention may exhibit a standard deviation of tensile strength of 5.0 MPa or less.

More specifically, when the aliphatic diol compound is butane diol, the standard deviation of the tensile strength may be 4.0 MPa or less, 3.0 MPa or less, 2.0 MPa or less, 1.9 MPa or less, 1.8 MPa or less, or 1.75 MPa or less.

In one embodiment, when the aliphatic diol compound is a mixture of ethylene glycol and cyclohexanedimethanol, the polyester composite of the present invention may exhibit a standard deviation of tensile strength of 3.5 MPa or less.

More specifically, when the aliphatic diol compound is a mixture of ethylene glycol and cyclohexanedimethanol, the standard deviation of the tensile strength may be 3.0 MPa or less, 2.5 MPa or less, 2.0 MPa or less, 1.9 MPa or less, or 1.85 MPa or less. .

The tensile strength standard deviation may be, for example, the standard deviation of values measured for five specimens using a universal testing machine (UTM) according to ASTM D638.

According to another aspect of the present invention, the nanomaterial is a solid dispersion of anhydrosugar alcohol dispersed therein, and a diol component comprising an aliphatic diol compound selected from ethylene glycol, butanediol, cyclohexanedimethanol, or a mixture thereof and a polymerization reaction of the dicarboxyl component, wherein the solid dispersion of the anhydrosugar alcohol is obtained by introducing the nanomaterial into the anhydrosugar alcohol in an aqueous dispersion state, a method for producing a polyester composite is provided .

In one embodiment, the solid dispersion of the anhydrosugar alcohol is added to the anhydrosugar alcohol in an aqueous dispersion state of the nanomaterial (eg, a state in which the nanomaterial is dispersed in water at a concentration of 0.1 to 5% by weight) and uniformly After mixing and melting while removing moisture by applying a vacuum at a temperature above the melting point of the anhydrosugar alcohol (for example, at a temperature of 80° C. or higher), it may be a room temperature solid dispersion obtained by cooling the molten mixture to room temperature.

Nanomaterials, anhydrosugar alcohols, aliphatic diol compounds, dicarboxyl components, and diol components that can be additionally used in the manufacturing method are as described above. In addition, the solid dispersion of the anhydrosugar alcohol and its manufacturing method are the same as described above.

In one embodiment, the method for preparing the polyester composite includes (1) an aliphatic diol compound selected from the solid dispersion of the anhydrosugar alcohol, and ethylene glycol, butane diol, cyclohexanedimethanol, or a mixture thereof. subjecting the diol component and the dicarboxyl component to an esterification reaction or a transesterification reaction; and (2) subjecting the reaction product obtained in step (1) to a polycondensation reaction.

In one embodiment, in step (1), the solid dispersion of the anhydrosugar alcohol, and a diol component comprising an aliphatic diol compound selected from ethylene glycol, butane diol, cyclohexanedimethanol, or a mixture thereof and a diol The carboxyl component is introduced into the reactor so that the reaction molar ratio of the diol component to the dicarboxyl component (total moles of diol components/total moles of dicarboxyl components) is 1.0 to 1.5, and then 150 to 250° C. (more specifically, The esterification reaction or transesterification reaction is performed at a temperature of 200 to 250 ° C or 200 to 240 ° C) and a pressure condition (reduced pressure condition) of 0.1 to 3.0 kgf/cm 2 (more specifically, 0.2 to 2.0 kgf/cm 2 ). can be

The esterification reaction time or transesterification reaction time is usually 1 to 5 hours, more specifically about 3 to 4 hours, and may vary depending on the reaction temperature and pressure, and the reaction molar ratio of the dicarboxyl component to the diol component.

A catalyst is not necessarily required for the esterification reaction or the transesterification reaction (step (1) above), but a catalyst may be used to shorten the reaction time. The esterification reaction or transesterification reaction (step (1) above) may be performed in a batch or continuous manner, and each reaction raw material may be separately input.

In one embodiment, in step (2), a polycondensation reaction of the reaction product obtained in step (1) is performed.

Before the start of the polycondensation reaction, a polycondensation catalyst and a stabilizer may be added to the reaction product of the esterification reaction or the transesterification reaction. As the polycondensation catalyst, a polycondensation catalyst commonly used in this field may be used without limitation, for example, a titanium-based compound, a germanium-based compound, an antimony-based compound, an aluminum-based compound, and a tin-based compound. One type or a mixture of two or more types may be used. As the stabilizer added to the polycondensation reaction, a phosphorus-based compound may be generally used, and for example, phosphoric acid, trimethyl phosphate, triethyl phosphate, or a mixture thereof may be used.

The polycondensation reaction is carried out at a temperature of 200 to 280 °C (more specifically, 210 to 260 °C or 220 to 240 °C) and a reduced pressure of 500 to 0.1 mmHg. The reduced pressure condition is for removing by-products of the polycondensation reaction.

In one embodiment, the polyester composite of the present invention comprises (a) (i) a dicarboxyl component comprising dimethyl terephthalate; And (ii) a solid dispersion of anhydrosugar alcohol, and a polymerization reaction product comprising a diol component comprising an aliphatic diol compound selected from ethylene glycol, butane diol, cyclohexanedimethanol or mixtures thereof, at atmospheric pressure or 0.1 to 3.0 The esterification reaction or transesterification reaction is carried out at a pressurization pressure of kgf/cm 2 and a temperature of 150 to 250° C. for an average residence time of 1 to 5 hours. (b) Next, the esterification or transesterification reaction product is subjected to a polycondensation reaction under a reduced pressure condition of 500 to 0.1 mmHg and a temperature of 200 to 280° C. for an average residence time of 1 to 10 hours, so that the polycondensation reaction according to the present invention An ester complex can be prepared. Preferably, the final vacuum degree of the polycondensation reaction is 1.0 mmHg or less, and the esterification or transesterification reaction may be performed under an inert gas atmosphere.

According to another aspect of the present invention, there is provided a molded article comprising the polyester composite of the present invention.

The polyester composite of the present invention can have uniform physical properties (especially, tensile strength, tensile modulus and elongation, etc.) because the nanomaterial is uniformly dispersed in the composite. The defect rate can be very low when applying the product.

A method of molding the polyester composite of the present invention to produce a molded article is not particularly limited, and a molded article may be manufactured using a method generally used in the field of plastic molding. For example, the molded article of the present invention may be manufactured by extruding or injection molding the polyester composite of the present invention.

Hereinafter, the present invention will be described in more detail through Examples and Comparative Examples. However, the scope of the present invention is not limited thereto.

[ Example ]

[Solid containing nanocellulose dispersion Produce]

<Nano cellulose fiber ( Nanocellulose fiber( NCF ))Wow no sugar containing alcohol dispersion >

production example A1: Nano Cellulose Fiber 1 by weight % containing dispersion Produce

In a rotary concentrator, 99 g of isosorbide (NOVASORB® Samyang Co., Ltd.) and 100 g of an aqueous solution (KB101, Asia Nano Cellulose Co., Ltd.) in which nanocellulose fibers are dispersed at 1 wt% (KB101, Asia Nano Cellulose Co., Ltd.) were uniformly mixed. Thereafter, the mixture was melted while removing moisture by applying a vacuum under a temperature condition of 80° C. or higher than the melting point of isosorbide. Then, the molten mixture was cooled to room temperature to prepare isosorbide (solid dispersion) in which nano-cellulose fibers were dispersed. The solid dispersion, based on the total weight of the solid dispersion, included 1% by weight of nano-cellulose fibers.

production example A2: 3 nano cellulose fibers by weight % containing dispersion Produce

Except that the content of isosorbide was changed from 99 g to 97 g, and the content of the aqueous solution in which the nano cellulose fibers were dispersed at 1 wt % was changed from 100 g to 300 g, it was carried out in the same manner as in Preparation Example A1. Isosorbide (solid dispersion) in which fibers were dispersed was prepared. The solid dispersion, based on the total weight of the solid dispersion, contained 3% by weight of nano-cellulose fibers.

production example A3: 5 nano cellulose fibers by weight % containing dispersion Produce

Except that the content of isosorbide was changed from 99 g to 95 g, and the content of the aqueous solution in which the nano cellulose fibers were dispersed at 1 wt % was changed from 100 g to 500 g, it was carried out in the same manner as in Preparation Example A1 to nano cellulose Isosorbide (solid dispersion) in which fibers were dispersed was prepared. The solid dispersion, based on the total weight of the solid dispersion, contained 5% by weight of nano-cellulose fibers.

production example A4: 10 nano cellulose fibers by weight % containing dispersion Produce

Except that the content of isosorbide was changed from 99 g to 90 g, and the content of the aqueous solution in which the nano cellulose fibers were dispersed at 1 wt % was changed from 100 g to 1,000 g, it was performed in the same manner as in Preparation Example A1. An isosorbide (solid dispersion) in which cellulose fibers were dispersed was prepared. The solid dispersion, based on the total weight of the solid dispersion, contained 10% by weight of nano cellulose fibers.

<Nano cellulose crystals ( Nanocellulose crystal (NCC)) and no sugar containing alcohol dispersion >

production example B1: Nanocellulose crystals 1 by weight % containing dispersion Produce

Instead of 100 g of aqueous solution (KB101, Asia Nano Cellulose Co., Ltd.) in which nanocellulose fibers are dispersed at 1 wt% , to prepare isosorbide (solid dispersion) in which nano-cellulose crystals are dispersed in the same manner as in Preparation Example A1. The solid dispersion, based on the total weight of the solid dispersion, contained 1% by weight of nano cellulose crystals.

production example B2: Nanocellulose crystals 3 by weight % containing dispersion Produce

The content of isosorbide was changed from 99 g to 97 g, and 300 g of an aqueous solution in which nano cellulose crystals were dispersed at 1 wt % was used instead of 100 g of the aqueous solution in which nano cellulose fibers were dispersed at 1 wt %, except that 300 g of the aqueous solution was used. It was carried out in the same manner as A1 to prepare isosorbide (solid dispersion) in which nano cellulose crystals were dispersed. The solid dispersion, based on the total weight of the solid dispersion, contained 3% by weight of nano cellulose crystals.

production example B3: nano cellulose crystals 5 by weight % containing dispersion Produce

The content of isosorbide was changed from 99 g to 95 g, and 500 g of an aqueous solution in which nano cellulose crystals were dispersed at 1 wt % was used instead of 100 g of an aqueous solution in which nano cellulose fibers were dispersed at 1 wt %, except that 500 g of the aqueous solution was used. It was carried out in the same manner as A1 to prepare isosorbide (solid dispersion) in which nano cellulose crystals were dispersed. The solid dispersion, based on the total weight of the solid dispersion, contained 5% by weight of nano cellulose crystals.

production example B4: nano cellulose crystals 10 by weight % containing dispersion Produce

The content of isosorbide was changed from 99 g to 90 g, and 1,000 g of an aqueous solution in which nano cellulose crystals were dispersed at 1 wt % was used instead of 100 g of an aqueous solution in which nano cellulose fibers were dispersed at 1 wt %. Isosorbide (solid dispersion) in which nanocellulose crystals were dispersed was prepared in the same manner as in Example A1. The solid dispersion, based on the total weight of the solid dispersion, contained 10% by weight of nano cellulose crystals.

<A mixture of nanocellulose fibers and nanocellulose crystals and no sugar containing alcohol dispersion >

production example C1: A mixture of nanocellulose fibers and nanocellulose crystals 1 by weight % containing dispersion Produce

Except for using a mixture of 50 g of an aqueous solution in which nano cellulose fibers are dispersed at 1 wt % and 50 g of an aqueous solution in which nano cellulose crystals are dispersed at 1 wt % instead of 100 g of an aqueous solution in which nano cellulose fibers are dispersed at 1 wt %, Isosorbide (solid dispersion) in which nano-cellulose fibers and nano-cellulose crystals were dispersed was prepared in the same manner as in Preparation Example A1. The solid dispersion contained 1% by weight of a mixture of nano-cellulose fibers and nano-cellulose crystals, based on the total weight of the solid dispersion.

production example C2: a mixture of nanocellulose fibers and nanocellulose crystals 3 by weight % containing dispersion Produce

The content of isosorbide was changed from 99 g to 97 g, and instead of 100 g of the aqueous solution in which the nano cellulose fibers were dispersed at 1 wt %, 150 g of the aqueous solution in which the nano cellulose fibers were dispersed at 1 wt % and the nano cellulose crystals were dispersed at 1 wt % Isosorbide (solid dispersion) in which nano-cellulose fibers and nano-cellulose crystals were dispersed was prepared in the same manner as in Preparation Example A1, except that a mixture of 150 g of an aqueous solution was used. The solid dispersion contained 3 wt% of a mixture of nano-cellulose fibers and nano-cellulose crystals, based on the total weight of the solid dispersion.

production example C3: a mixture of nanocellulose fibers and nanocellulose crystals 5 by weight % containing dispersion Produce

The content of isosorbide was changed from 99 g to 95 g, and instead of 100 g of the aqueous solution in which the nano cellulose fibers were dispersed at 1 wt %, 250 g of the aqueous solution in which the nano cellulose fibers were dispersed at 1 wt % and the nano cellulose crystals were dispersed at 1 wt % Except that a mixture of 250 g of the aqueous solution was used, isosorbide (solid dispersion) in which nano-cellulose fibers and nano-cellulose crystals were dispersed was prepared in the same manner as in Preparation Example A1. The solid dispersion contained 5 wt% of a mixture of nano-cellulose fibers and nano-cellulose crystals, based on the total weight of the solid dispersion.

production example C4: containing a mixture of nano-cellulose fibers and nano-cellulose crystals in an amount of 10% by weight dispersion Produce

The content of isosorbide was changed from 99 g to 90 g, and instead of 100 g of the aqueous solution in which the nano cellulose fibers were dispersed at 1 wt %, 500 g of the aqueous solution in which the nano cellulose fibers were dispersed at 1 wt % and the nano cellulose crystals were dispersed at 1 wt % Isosorbide (solid dispersion) in which nano-cellulose fibers and nano-cellulose crystals were dispersed was prepared in the same manner as in Preparation Example A1, except that a mixture of 500 g of an aqueous solution was used. The solid dispersion contained 10% by weight of a mixture of nano-cellulose fibers and nano-cellulose crystals, based on the total weight of the solid dispersion.

[Solid containing nanocellulose dispersion Polyester resin composite using]

<Preparation of a polyester resin composite using a solid dispersion containing nanocellulose fibers and anhydrosugar alcohol and evaluation of physical properties>

Example A1: production example A1 solid dispersion Polyester resin composite production using

Put the reactants of the composition shown in Table 1 below in a 5L melt-condensation reactor, add 550 ppm of a titanium-based catalyst based on the acid component (dimethyl terephthalate, DMT), and then increase the temperature to 210 ° C. alcohol was removed. When more than 80% of the alcohol is leaked compared to the theoretical amount of alcohol generated, 750 ppm of a titanium-based catalyst and antioxidant are added, and the pressure of the reaction system is gradually reduced to 1 mmHg while raising the temperature to 245° C. to prepare a thermoplastic polyester resin composite did.

In order to measure the nanocellulose fiber content in the obtained thermoplastic polyester resin composite, 50 g of the thermoplastic polyester resin composite was dissolved in 1 L of chloroform, and the remaining crystalline components were filtered, dried in a vacuum oven for about 24 hours, and the As a result of measuring the weight, it was 0.075 g. Through this, the content of the nano-cellulose fibers in the obtained thermoplastic polyester resin composite was calculated to be 0.15% by weight.

Five identical tensile specimens were prepared according to ASTM D638 using the obtained thermoplastic polyester resin composite, and the tensile strength of the five tensile specimens was measured using a universal testing machine (UTM). As a result, the average tensile strength was 51 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 1 below.

Example A2: production example A2 solid dispersion Polyester resin composite production using

A reactant having the composition shown in Table 1 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the content of nanocellulose fibers in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.60 wt%, and the average of the obtained thermoplastic polyester resin composite in the same manner as in Example A1. As a result of measuring the tensile strength, it was 53 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 1 below.

Example A3: production example A3 solid dispersion Polyester resin composite production using

A reactant having the composition shown in Table 1 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the content of nano-cellulose fibers in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.75 wt%, and the average of the obtained thermoplastic polyester resin composite in the same manner as in Example A1. As a result of measuring the tensile strength, it was 54 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 1 below.

Example A4: production example A4 solid dispersion Polyester resin composite production using

A reactant having the composition shown in Table 1 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the content of nano-cellulose fibers in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.50 wt %, and the average of the obtained thermoplastic polyester resin composite in the same manner as in Example A1. As a result of measuring the tensile strength, it was 58 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 1 below.

<Nanocellulose crystals and no sugar solids containing alcohol dispersion Preparation of polyester resin composite using and evaluation of physical properties>

Example B1: production example B1 solid dispersion Polyester resin composite production using

A reactant having the composition shown in Table 1 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the content of nano cellulose crystals in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.20 wt %, and the average of the obtained thermoplastic polyester resin composite in the same manner as in Example A1. As a result of measuring the tensile strength, it was 110.2 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 1 below.

Example B2: production example B2 solid dispersion Polyester resin composite production using

A reactant having the composition shown in Table 1 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the content of nano cellulose crystals in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.30 wt%, and the average of the obtained thermoplastic polyester resin composite in the same manner as in Example A1. As a result of measuring the tensile strength, it was 120 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 1 below.

Example B3: production example B3 solid dispersion Polyester resin composite production using

A reactant having the composition shown in Table 1 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the content of nano cellulose crystals in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.50 wt%, and the average of the obtained thermoplastic polyester resin composite in the same manner as in Example A1. As a result of measuring the tensile strength, it was 120.8 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 1 below.

Example B4: production example B4 solid dispersion Polyester resin composite production using

A reactant having the composition shown in Table 1 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the content of nano cellulose crystals in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.50 wt%, and the average of the obtained thermoplastic polyester resin composite in the same manner as in Example A1. As a result of measuring the tensile strength, it was 121.6 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 1 below.

<A mixture of nanocellulose fibers and nanocellulose crystals and no sugar solids containing alcohol dispersion Preparation of polyester resin composite using and evaluation of physical properties>

Example C1: production example solid of C1 dispersion Polyester resin composite production using

A reactant having the composition shown in Table 1 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the total content of nano-cellulose fibers and nano-cellulose crystals in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.20 wt%, and in the same manner as in Example A1, the obtained thermoplastic poly As a result of measuring the average tensile strength of the ester resin composite, it was 34.6 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 1 below.

Example C2: production example C2 solid dispersion Polyester resin composite production using

A reactant having the composition shown in Table 1 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the total content of nano-cellulose fibers and nano-cellulose crystals in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.30 wt%, and in the same manner as in Example A1, the obtained thermoplastic poly As a result of measuring the average tensile strength of the ester resin composite, it was 34.6 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 1 below.

Example C3: production example C3 solid dispersion Polyester resin composite production using

A reactant having the composition shown in Table 1 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the total content of nano-cellulose fibers and nano-cellulose crystals in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.25 wt%, and in the same manner as in Example A1, the obtained thermoplastic poly As a result of measuring the average tensile strength of the ester resin composite, it was 35.2 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 1 below.

Example C4: production example C4 solid dispersion Polyester resin composite production using

A reactant having the composition shown in Table 1 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the total content of nano-cellulose fibers and nano-cellulose crystals in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 1.0 wt%, and in the same manner as in Example A1, the obtained thermoplastic poly As a result of measuring the average tensile strength of the ester resin composite, it was 44 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 1 below.

[Table 1]

[ comparative example ]

comparative example A1: Nanocellulose particles are not dispersed no sugar Polyester resin manufacturing and physical property evaluation using alcohol

It was carried out in the same manner as in Example A1, except that pure isosorbide (NOVASORB® Samyang Corporation) was used instead of the solid dispersion prepared in Preparation Example A1, and the reactants of the composition shown in Table 2 below were The reaction was carried out to obtain a thermoplastic polyester resin. As a result of measuring the average tensile strength of the obtained thermoplastic polyester resin in the same manner as in Example A1, the average tensile strength was 46 MPa.

The obtained thermoplastic polyester resin was evaluated for physical properties, and the results are shown in Table 2 below.

The thermoplastic polyester resin of Comparative Example A1 that does not contain nano-cellulose particles has a relatively low average tensile strength compared to the thermoplastic polyester resin composite of Examples A1 to A4 according to the present invention, confirming that the mechanical properties are poor. (The thermoplastic polyester resin of Comparative Example A1 and the thermoplastic polyester resin composite of Examples A1 to A4 have the same monomer components (DMT, EG and ISB)).

comparative example B1: Nano Cellulose Fiber Powder 1 by weight % melt containing dispersion Polyester resin composite manufacturing and physical property evaluation using

99 g of isosorbide (NOVASORB® Samyang Co., Ltd.) was heated in an oven at 70° C. to obtain 99 g of molten isosorbide. 1 g of nano cellulose fibers in powder form were directly added to 99 g of the molten isosorbide, and the nanocellulose fibers were dispersed in the molten isosorbide by stirring. After that, it was further dispersed for about 1 hour using an ultrasonicator at the same temperature to prepare isosorbide (liquid molten dispersion) in which nanocellulose fibers were dispersed. The molten dispersion, based on the total weight of the molten dispersion, included 1% by weight of nano cellulose fibers.

Thereafter, a reactant having the composition shown in Table 2 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the content of nanocellulose fibers in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.15% by weight, and the average tensile strength of the obtained thermoplastic polyester resin composite in the same manner as in Example A1. As a result of measuring the strength, the average tensile strength was 46 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 2 below.

Compared with the thermoplastic polyester resin composite of Examples A1 to A4 according to the present invention, the thermoplastic polyester resin composite of Comparative Example B1 had a relatively low average tensile strength, and it was confirmed that mechanical properties were poor (Comparative Example B1 of the thermoplastic polyester resin composite and the thermoplastic polyester resin composite of Examples A1 to A4 have the same monomer components (DMT, EG and ISB).

comparative example B2: Nano Cellulose Fiber Powder 10 by weight % melt containing dispersion Polyester resin composite manufacturing and physical property evaluation using

Except that the content of isosorbide was changed from 99g to 90g and the content of nanocellulose fibers in powder form was changed from 1g to 10g, it was carried out in the same manner as in Comparative Example B1, so that the nanocellulose fibers were dispersed iso A sorbide (liquid molten dispersion) was obtained. The molten dispersion, based on the total weight of the molten dispersion, contained 10% by weight of nano cellulose fibers.

Thereafter, a reactant having the composition shown in Table 2 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the content of nano-cellulose fibers in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.50 wt %, and the average of the obtained thermoplastic polyester resin composite in the same manner as in Example A1. As a result of measuring the tensile strength, it was 47.8 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 2 below.

Compared to the thermoplastic polyester resin composite of Examples A1 to A4 according to the present invention, the thermoplastic polyester resin composite of Comparative Example B2 had a relatively low average tensile strength, and it was confirmed that mechanical properties were poor (Comparative Example B2 of the thermoplastic polyester resin composite and the thermoplastic polyester resin composite of Examples A1 to A4 have the same monomer components (DMT, EG and ISB).

comparative example C1: Nanocellulose crystal powder 1 by weight % melt containing dispersion Polyester resin composite manufacturing and physical property evaluation using

Isosorbide (liquid molten dispersion) in which nanocellulose crystals are dispersed in the same manner as in Comparative Example B1, except that 1g of powdered nanocellulose crystals was used instead of 1g of powdered nanocellulose fibers was obtained. The molten dispersion, based on the total weight of the molten dispersion, contained 1% by weight of nano cellulose crystals.

Thereafter, a reactant having the composition shown in Table 2 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the content of nano cellulose crystals in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.20 wt %, and the average of the obtained thermoplastic polyester resin composite in the same manner as in Example A1. As a result of measuring the tensile strength, it was 105.4 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 2 below.

Compared to the thermoplastic polyester resin composite of Examples B1 to B4 according to the present invention, the thermoplastic polyester resin composite of Comparative Example C1 had a relatively low average tensile strength, and it was confirmed that mechanical properties were poor (Comparative Example C1 of the thermoplastic polyester resin composite and the thermoplastic polyester resin composite of Examples B1 to B4 have the same monomer components (DMT, 1,4-BDO and ISB).

comparative example C2: nano cellulose crystal powder 10 by weight % melt containing dispersion Polyester resin composite manufacturing and physical property evaluation using

The content of isosorbide was changed from 99 g to 90 g, and 10 g of nano cellulose crystals in powder form were used instead of 1 g of nano cellulose fibers in powder form. This dispersed isosorbide (liquid molten dispersion) was obtained. The molten dispersion, based on the total weight of the molten dispersion, contained 10% by weight of nano cellulose crystals.

Thereafter, a reactant having the composition shown in Table 2 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the content of nano cellulose crystals in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.50 wt%, and the average of the obtained thermoplastic polyester resin composite in the same manner as in Example A1. As a result of measuring the tensile strength, it was 108.8 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 2 below.

Compared to the thermoplastic polyester resin composite of Examples B1 to B4 according to the present invention, the thermoplastic polyester resin composite of Comparative Example C2 had a relatively low average tensile strength, and it was confirmed that mechanical properties were poor (Comparative Example C2 of the thermoplastic polyester resin composite and the thermoplastic polyester resin composite of Examples B1 to B4 have the same monomer components (DMT, 1,4-BDO and ISB).

comparative example D1: Nano Cellulose Fiber Powder 1 by weight % melt containing dispersion Polyester resin composite manufacturing and physical property evaluation using

It was carried out in the same manner as in Comparative Example B1 to obtain isosorbide (liquid molten dispersion) in which nano-cellulose fibers were dispersed. The molten dispersion, based on the total weight of the molten dispersion, included 1% by weight of nano cellulose fibers.

Thereafter, a reactant having the composition shown in Table 2 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the content of nanocellulose fibers in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 0.20 wt%, and the average of the obtained thermoplastic polyester resin composite in the same manner as in Example A1. As a result of measuring the tensile strength, it was 30.6 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 2 below.

Compared to the thermoplastic polyester resin composite of Examples C1 to C4 according to the present invention, the thermoplastic polyester resin composite of Comparative Example D1 had a relatively low average tensile strength, and it was confirmed that mechanical properties were poor (Comparative Example D1 of the thermoplastic polyester resin composite and the thermoplastic polyester resin composite of Examples C1 to C4 have the same monomer components (DMT, EG, 1,4-CHDM and ISB).

comparative example D2: Nano Cellulose Fiber Powder 10 by weight % melt containing dispersion Polyester resin composite manufacturing and physical property evaluation using

Except that the content of isosorbide was changed from 99g to 90g and the content of nanocellulose fibers in powder form was changed from 1g to 10g, it was carried out in the same manner as in Comparative Example B1, so that the nanocellulose fibers were dispersed iso A sorbide (liquid molten dispersion) was obtained. The molten dispersion, based on the total weight of the molten dispersion, contained 10% by weight of nano cellulose fibers.

Thereafter, a reactant having the composition shown in Table 2 was put into a 5L melt-condensation reactor, and a thermoplastic polyester resin composite was prepared in the same manner as in Example A1. As a result of measuring the content of nano-cellulose fibers in the obtained thermoplastic polyester resin composite in the same manner as in Example A1, it was 1.0 wt %, and the average of the obtained thermoplastic polyester resin composite in the same manner as in Example A1. As a result of measuring the tensile strength, it was 29.8 MPa.

The obtained thermoplastic polyester resin composite was evaluated for physical properties, and the results are shown in Table 2 below.

Compared to the thermoplastic polyester resin composite of Examples C1 to C4 according to the present invention, the thermoplastic polyester resin composite of Comparative Example D2 had a relatively low average tensile strength, and it was confirmed that mechanical properties were poor (Comparative Example D2 of the thermoplastic polyester resin composite and the thermoplastic polyester resin composite of Examples C1 to C4 have the same monomer components (DMT, EG, 1,4-CHDM and ISB).

[Table 2]

<Evaluation of dispersion uniformity of nano cellulose particles in polyester resin composite>

Tensile strength for each of the five tensile specimens of the thermoplastic polyester resin composites obtained in Examples A1 to A4, B1 to B4, and C1 to C4 and Comparative Examples B1, B2, C1, C2, D1 and D2 above, and Their average values and standard deviations were measured and shown in Table 3 below.

[Table 3]

[Evaluation of physical properties]

The evaluation of physical properties of the thermoplastic polyester resin composites prepared in Examples and Comparative Examples was performed as follows.

(1) Intrinsic Viscosity (IV): After dissolving a polyester resin composite in a mixture of phenol and tetrachloroethane (weight ratio = 50:50) to prepare a 0.5 wt% solution, intrinsic viscosity at 35°C using an Uberod viscometer was measured.

(2) Tensile strength: According to ASTM D638, the tensile strength was measured using a universal testing machine (UTM).

As shown in Table 3, the thermoplastic polyester resin composite of Examples A1 to A4 according to the present invention is a solid dispersion prepared by dispersing an aqueous dispersion containing nanocellulose particles in anhydrosugar alcohol, nanocellulose Compared with the thermoplastic polyester resin containing no particles (Comparative Example A1), mechanical properties (tensile strength) were remarkably improved.

In particular, as a result of measuring the average and standard deviation of the tensile strength of five tensile specimens of each of the thermoplastic polyester resin composites of Examples A1 to A4 according to the present invention, the standard deviation range of the tensile strength of the five tensile specimens is 1.79 MPa or less. As a result, the tensile strengths of the five tensile specimens were equal to each other, and the variation in tensile strength was low. In addition, as a result of measuring the average and standard deviation of the tensile strength of five tensile specimens of each of the thermoplastic polyester resin composites of Examples B1 to B4 according to the present invention, the standard deviation range of the tensile strength of the five tensile specimens is 1.72 MPa or less As the tensile strength of the five tensile specimens was equal to each other, the tensile strength deviation was low, and the average and standard deviation of the tensile strength of the five tensile specimens of each of the thermoplastic polyester resin composites of Examples C1 to C4 according to the present invention were measured. As a result, the standard deviation of the tensile strengths of the five tensile specimens was in the range of 1.85 MPa or less, and the tensile strengths of the five tensile specimens were equal to each other. From this, it can be seen that the nano-cellulose particles are uniformly dispersed in the thermoplastic polyester resin composite according to the present invention.

On the other hand, the thermoplastic polyester resin of Comparative Example A1 did not contain nano-cellulose particles, and mechanical properties were remarkably poor compared to the thermoplastic polyester resin composites of Examples A1 to A4 according to the present invention.

In addition, as shown in Table 3, in the case of the thermoplastic polyester resin composites of Comparative Examples B1, B2, C1, C2, D1 and D2 not according to the present invention, the nanocellulose particles are uniformly dispersed in the thermoplastic polyester resin composite, Therefore, there was a large variation in tensile strength depending on the tensile specimen to be measured.

Specifically, as a result of measuring the average and standard deviation of the tensile strength of five tensile specimens of each of the thermoplastic polyester resin composites of Comparative Examples B1 and B2, the standard deviation range of the tensile strength of the five tensile specimens was 4.77 MPa to 5.27 MPa. The variation in strength was very large, and as a result of measuring the average and standard deviation of the tensile strength of five tensile specimens of each of the thermoplastic polyester resin composites of Comparative Examples C1 and C2, the standard deviation of the tensile strength of the five tensile specimens was 5.31 MPa to The deviation of the tensile strength was very large at 9.22 MPa, and as a result of measuring the average and standard deviation of the tensile strength of five tensile specimens of each of the thermoplastic polyester resin composites of Comparative Examples D1 and D2, the standard deviation of the tensile strength of five tensile specimens was measured. In the range of 3.88 MPa to 6.11 MPa, the variation in tensile strength was very large. This indicated that the nano-cellulose particles were non-uniformly dispersed in the thermoplastic polyester resin composite.

As described above, the tensile strength of the thermoplastic polyester resin composite may be different depending on the type of aliphatic diol used, but when comparing the thermoplastic polyester resin composites containing the same monomer, that is, compared with Examples A1 to A4 The thermoplastic polyester resin composite of Examples B1 and B2, or the thermoplastic polyester resin composite of Examples B1 to B4 and Comparative Examples C1 and C2, or the thermoplastic polyester of Examples C1 to C4 and Comparative Examples D1 and D2 In case of preparing the resin composite, the thermoplastic polyester resin composite of the embodiment according to the present invention has nano-cellulose particles uniformly dispersed in the composite, and thus has high tensile strength and high tensile strength, and can exhibit uniform physical properties, but not according to the present invention In the thermoplastic polyester resin composite of the comparative example, the nano-cellulose particles are not uniformly dispersed in the composite, and, compared to the polyester resin composite of the embodiment according to the present invention, relatively poor tensile strength is implemented, and uniform physical properties are not shown. can confirm that it is not.

Claims (18)

A polyester composite comprising:
It includes a matrix resin and a nanomaterial dispersed in the matrix resin,
Here, the matrix resin is a solid dispersion of anhydrosugar alcohol in which the nanomaterial is dispersed, and a diol component comprising an aliphatic diol compound selected from ethylene glycol, butanediol, cyclohexanedimethanol, or a mixture thereof; It is a polyester resin that is a polymerization reaction product of a dicarboxyl component,
The solid dispersion of the anhydrosugar alcohol is obtained by introducing the nanomaterial into the anhydrosugar alcohol in an aqueous dispersion state,
wherein the composite exhibits a tensile strength standard deviation of 4.5 MPa or less;
polyester composite. According to claim 1, wherein the nanomaterial is nanocellulose, carbon nanofibers, carbon nanotubes, iron, aluminum, chromium, nickel, cobalt, zinc, tungsten, indium, tin, palladium, zirconium, titanium, copper, silver, gold , platinum, kaolin, clay, talc, mica, silica, bentonite, dolomite, calcium silicate, magnesium silicate, asbestos, calcium carbonate, magnesium carbonate, barium carbonate, calcium sulfate, barium sulfate, aluminum sulfate, aluminum hydroxide, iron hydroxide, aluminum silicate , zirconium oxide, magnesium oxide, aluminum oxide, titanium oxide, iron oxide, zinc oxide, antimony trioxide, indium oxide, indium tin oxide, silicon carbide, silicon nitride, boron nitride, barium titanate, diatomaceous earth, carbon black, rock wool, graphene, graphite , graphene oxide, azo-based compound, diazo-based compound, condensed azo-based compound, thioindigo-based compound, indanthrone-based compound, quinacrindone-based compound, anthraquinone-based compound, benzimidazolone-based compound, perylene-based compound, phthalocyanine compound, anthrapyridine compound, dioxazine compound, polyethylene resin, polypropylene resin, polyester resin, nylon resin, polyamide resin, aramid resin, urethane resin, polystyrene resin, polylactic acid, cellulose acetate fiber, hemicellulose, lignin, A polyester composite, which is selected from chitin, chitosan, starch, or mixtures thereof. The polyester composite according to claim 1, wherein the nanomaterial is selected from nanocellulose, carbon nanofibers, carbon nanotubes, or mixtures thereof. 4. Poly according to claim 3, wherein the nanocellulose is selected from nanocellulose fibers, nanocellulose crystals or mixtures thereof, and wherein the carbon nanotubes are selected from single-walled carbon nanotubes, multi-walled carbon nanotubes or mixtures thereof. ester complex. According to claim 1, wherein the content of the nanomaterial, based on the total weight of the composite, 0.1% to 10% by weight, polyester composite. The polyester composite according to claim 1, wherein the anhydrosugar alcohol is a mono-anhydrosugar alcohol, a dianhydrosugar alcohol, or a mixture thereof. The method according to claim 1, wherein the solid dispersion of the anhydrosugar alcohol is mixed with the nanomaterial in an aqueous dispersion state, and melted while removing moisture at a temperature above the melting point of the anhydrosugar alcohol, and then melted What is obtained by cooling the mixture to room temperature, the polyester composite. The polyester composite of claim 1, wherein the dicarboxyl component is selected from an aliphatic dicarboxyl compound, an aromatic dicarboxyl compound, or a combination thereof. According to claim 1, wherein the diol component, in addition to the solid dispersion of the anhydrosugar alcohol, and an aliphatic diol compound selected from ethylene glycol, butane diol, cyclohexanedimethanol or mixtures thereof, further comprising an additional diol component which is a polyester composite. The polyester composite according to claim 1, wherein the aliphatic diol compound is ethylene glycol, and the composite exhibits a tensile strength of 48 MPa or more. The polyester composite according to claim 1, wherein the aliphatic diol compound is butane diol, and the composite exhibits a tensile strength of at least 109 MPa. The polyester composite according to claim 1, wherein the aliphatic diol compound is a mixture of ethylene glycol and cyclohexanedimethanol, and the composite exhibits a tensile strength of at least 31 MPa. The polyester composite according to claim 1, wherein the aliphatic diol compound is ethylene glycol. The polyester composite according to claim 1, wherein the aliphatic diol compound is butane diol. The polyester composite according to claim 1, wherein the aliphatic diol compound is a mixture of ethylene glycol and cyclohexanedimethanol. A method for producing a polyester composite, comprising:
Polymerization of a diol component and a dicarboxyl component comprising a solid dispersion of anhydrosugar alcohol dispersed therein, and an aliphatic diol compound selected from ethylene glycol, butanediol, cyclohexanedimethanol, or a mixture thereof comprising the steps of
Here, the solid dispersion of the anhydrosugar alcohol is obtained by introducing the nanomaterial into the anhydrosugar alcohol in an aqueous dispersion state,
wherein the composite exhibits a tensile strength standard deviation of 4.5 MPa or less;
A method for producing a polyester composite. The method according to claim 16, wherein the solid dispersion of the anhydrosugar alcohol is mixed with the nanomaterial in an aqueous dispersion state, and melted while removing moisture at a temperature equal to or higher than the melting point of the anhydrosugar alcohol, and then melted A method for producing a polyester composite, which is obtained by cooling the mixture to room temperature. A molded article comprising the polyester composite of any one of claims 1 to 15.