JP4927449B2 - Antistatic biodegradable resin composition - Google Patents

Description

  The present invention relates to an antistatic resin composition. More specifically, an antistatic agent for a biodegradable resin excellent in the property of imparting permanent antistatic properties without inhibiting the biodegradability of the biodegradable resin, and the antistatic agent contained in the biodegradable resin It is related with the antistatic biodegradable resin composition which becomes.

  Conventionally, a method for imparting antistatic properties by mixing a biodegradable resin such as polylactic acid with a polyether, particularly polyethylene glycol or a modified product thereof, is well known. (For example, see Patent Documents 1 to 3)

JP-A-8-231837 JP-A-8-231838 JP-A-8-253665

However, although these methods provide antistatic properties, biodegradation in a natural environment is difficult, and the original biodegradability of the biodegradable resin is impaired.
The present invention relates to an antistatic agent that imparts a permanent antistatic property to a biodegradable resin without impairing the biodegradability, and an antistatic biodegradable resin composition containing the antistatic agent in a biodegradable resin. The purpose is to provide.

The inventors of the present invention have arrived at the present invention as a result of intensive studies to solve the above problems. That is, the present invention ^{is, 1 × 10 6 ~1 × 10} 10 Ω · cm in volume resistivity antistatic agent consisting of an ester group-containing polymer having (A), the biodegradable polyester resin (B) and ionic liquid ( and also contains the C3), the ratio of the ester group concentration per unit weight of the polymer and (B) [(mol / kg) / (mol / kg)] is 0.1 / 1 to 0.9 / 1 An antistatic biodegradable resin composition comprising: an antistatic agent for the composition (A); an antistatic resin molded product obtained by molding the composition; and the molded product. It is a molded article formed by painting and / or printing.

The antistatic biodegradable resin composition of the present invention and the antistatic agent for the composition have the following effects.
(1) The antistatic agent is excellent in dispersibility in a biodegradable polyester resin.
(2) A molded product formed by molding the antistatic biodegradable resin composition has excellent permanent antistatic properties and does not impair the original biodegradability of the biodegradable resin.

The antistatic biodegradable resin composition of the present invention is a biodegradable polyester comprising an antistatic agent (A) comprising an ester group-containing polymer having a volume resistivity of 1 × 10 ⁶ to 1 × 10 ¹⁰ Ω · cm. It is a composition characterized in that it is contained in the resin (B), and the ratio of the ester group concentration per unit weight between the polymer and (B) is 0.1 / 1 to 0.9 / 1. .

The polymer includes a block polymer containing at least a polyester block. Among these, from the viewpoint of antistatic properties, one selected from the group consisting of a polyether chain-containing block polymer (A1), an anionic group-containing block polymer (A2) and a cationic group-containing block polymer (A3) or Two or more block polymers. Hereinafter, (A1) to (A3) will be described.

[Polyether chain-containing block polymer (A1)]
(A1) is a block polymer comprising a polyester block (a) and a polyether chain-containing block (b), and is obtained by bonding (a) and (b) alternately and / or randomly.
Examples of (a) include a homopolymer of a biodegradable aliphatic polyester-forming monomer (a00), and a copolymer of (a00) and another monomer.
Examples of (a00) include oxycarboxylic acids having 2 to 6 carbon atoms (hereinafter abbreviated as C) [glycolic acid, lactic acid (DL, D and L), etc.], C4 to 6 lactides (DL, D) And L-form) and C3-16 lactones (propiolactone, butyrolactone, caprolactone, etc.). Of these, oxycarboxylic acids are preferable from the viewpoints of biodegradability and reactivity, lactic acid and lactide are more preferable, and L-lactic acid and L-lactide are particularly preferable.

Examples of other monomers copolymerized with (a00) include lactam (a01), aminocarboxylic acid (a02), diamine (a03), and dicarboxylic acid (a04).
The lactam (a01) includes C6-16, such as caprolactam, enantolactam, laurolactam, undecanolactam, and mixtures thereof.
Examples of the ring-opening polymer (a01) include nylon 4, nylon 5, nylon 6, nylon 8, and nylon 12.

As aminocarboxylic acid (a02), C6-16, for example, ω-aminocaproic acid, ω-aminoenanthic acid, ω-aminocaprylic acid, ω-aminopelargonic acid, ω-aminocapric acid, 11-aminoundecanoic acid, 12 -Aminododecanoic acid and mixtures thereof.
Examples of the self-polycondensate of (a02) include nylon 7 by polycondensation of ω-aminoenanthic acid, nylon 11 by polycondensation of ω-aminoundecanoic acid, and nylon 12 by polycondensation of 12-aminododecanoic acid. .

Diamine (a03) includes C2-40, such as aliphatic, alicyclic and aromatic (aliphatic) diamines, and mixtures thereof.
Aliphatic diamines include C2-40, such as ethylene diamine, propylene diamine, hexamethylene diamine, decamethylene diamine, 1,12-dodecane diamine, 1,18-octadecane diamine and 1,20-eicosane diamine.
Alicyclic diamines include C5-40, such as 1,3- and 1,4-cyclohexanediamine, isophorone diamine, 4,4'-diaminocyclohexylmethane and 2,2-bis (4-aminocyclohexyl) propane. It is done.
Examples of araliphatic diamines include C7-20, such as xylylenediamine, bis (aminoethyl) benzene, bis (aminopropyl) benzene, and bis (aminobutyl) benzene.
Aromatic diamines include C6-40, such as p-phenylenediamine, 2,4- and 2,6-toluylenediamine and 2,2-bis (4,4'-diaminophenyl) propane.

Examples of the dicarboxylic acid (a04) include C2-40 dicarboxylic acids such as aliphatic dicarboxylic acids, aromatic ring-containing dicarboxylic acids, alicyclic dicarboxylic acids, and derivatives of these dicarboxylic acids [for example, acid anhydrides, lower (C1-4) ) Alkyl esters and dicarboxylates [alkali metal (lithium, sodium, potassium, etc.) salts]] and mixtures of two or more thereof.

Examples of aliphatic dicarboxylic acids include C2-40 (preferably 4 to 20, more preferably 6 to 12 from the viewpoint of antistatic properties) saturated or unsaturated dicarboxylic acids such as succinic acid, glutaric acid, adipic acid, and pimelic acid. , Suberic acid, azelaic acid, sebacic acid, undecanedioic acid, dodecanedioic acid, maleic acid, fumaric acid and itaconic acid.
Examples of the aromatic ring-containing dicarboxylic acid include C8 to 40 (preferably 8 to 16, more preferably 8 to 14 from the viewpoint of antistatic properties), such as ortho-, iso- and terephthalic acid, 2,6- and 2,7. -Naphthalenedicarboxylic acid, diphenyl-4,4'-dicarboxylic acid, diphenoxyethanedicarboxylic acid, tolylene dicarboxylic acid and xylylene dicarboxylic acid.
As alicyclic dicarboxylic acid, C5-40 (preferably 6-18, more preferably 8-14 from the viewpoint of antistatic properties), for example, cyclopropanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, cyclohexenedicarboxylic acid, Examples include dicyclohexyl-4,4'-dicarboxylic acid and camphoric acid.

  Among the dicarboxylic acid derivatives, examples of the acid anhydride include anhydrides of the above dicarboxylic acids, such as maleic anhydride, itaconic anhydride and phthalic anhydride; examples of lower (C1-4) alkyl esters include lower alkyl esters of the above dicarboxylic acids, such as Dimethyl adipate and ortho-, iso- and dimethyl terephthalate; examples of the dicarboxylate include alkali metal salts of the above dicarboxylic acids such as sodium 5-sulfoisophthalate.

  Of these, aliphatic dicarboxylic acids and aromatic ring-containing dicarboxylic acids are preferable from the viewpoint of antistatic properties, and adipic acid, sebacic acid, terephthalic acid, isophthalic acid, and sodium 5-sulfoisophthalate are more preferable.

  The copolymerization ratio (weight ratio) of (a00) and the other monomer in the copolymer is usually 99.9 / 0.1 or less, and a biodegradable polyester resin (B) described later of the antistatic agent (A). The lower limit is preferably 50/50, more preferably 60/40, and the upper limit is preferably 95/5, more preferably 80/20 from the viewpoint of moldability.

Number average molecular weight of (a) [hereinafter abbreviated as Mn. The measurement is based on a gel permeation chromatography (GPC) method. ] Is preferably 800 to 25,000, more preferably 1,000 to 20,000 from the viewpoint of heat resistance of the molded product and reactivity with the polyether chain-containing block (b) described later.
The terminal group of (a) is preferably a group containing a carbonyl group (such as a carboxyl group) from the viewpoint of reactivity with (b).

As the polyether chain-containing block (b), an addition reaction of alkylene oxide (hereinafter abbreviated as AO) to diol (b01) or dihydric phenol (b02) represented by the following general formula (1) Is mentioned.

_{^{H- (OA 1) m -O-}} E 1 -O- (A 1 O) m '-H (1)

In the formula, E ¹ is a residue obtained by removing a hydroxyl group from an active hydrogen atom-containing compound, A ¹ is a C2-4 alkylene group, and a plurality of (A ¹ O) may be the same or different. It may be either block and / or random. m and m ′ represent an integer of 1 to 300, preferably 2 to 250, particularly preferably 10 to 100.

Diol (b01) includes aliphatic dihydric alcohol [C2-12 (preferably 2-8).
And more preferably 2-6) alkylene glycols such as ethylene glycol, propylene glycol, 1,2-, 1,3-, 2,3- and 1,4-butanediol, 1,2-, 1,3- 1,4-, 1,5-, 1,6-, 2,3-, 2,4-, 2,5- and 3,4-hexanediol, neopentyl glycol (hereinafter referred to as EG, PG, BD, respectively) , Abbreviated as HG and NPG.), 2,2-, 2,3-, 2,4-, 2,5-, 3,3- and 3,4-dimethyl-1,6-hexanediol and 1,12 -Dodecanediol]; alicyclic dihydric alcohol [C5-12 (preferably 5-10, more preferably 5-8), such as cyclopentane-1,2- and 1,3-diol, cyclohexane-1,2 -, 1,3- and 1,4-di Bis (hydroxymethyl) cyclohexane and hydrogenated bisphenol A]; aromatic ring-containing dihydric alcohols [C8-20, such as xylylene glycol, bis (hydroxymethyl) benzene and bis (hydroxyethyl) benzene]; and tertiary Amino group-containing diol [e.g., C1-12 aliphatic or alicyclic primary monoamine [methylamine, ethylamine, cyclopropylamine, 1-propylamine, 2-propylamine, amylamine, isoamylamine, hexylamine, 1, 3-dimethylbutylamine, 3,3-dimethylbutylamine, 2-aminoheptane, 3-aminoheptane, cyclopentylamine, hexylamine, cyclohexylamine, heptylamine, nonylamine, decylamine, undecylamine, Bishydroxyalkyl halides and aromatic primary monoamine C6～12 [aniline-decylamine, etc.], and a bis hydroxyalkyl compound] benzyl amine.
Of (b01), from the viewpoint of antistatic properties of (A1) and dispersibility of (A1) with respect to (B) described later, aliphatic dihydric alcohols are preferred, and EG is more preferred.

Examples of the dihydric phenol (b02) include monocyclic dihydric phenols (C6-18, such as hydroquinone, catechol, resorcin and urushiol), bisphenols (C12-20, such as bisphenol A, -F and -S, 4,4 ' -Dihydroxydiphenyl-2,2-butane and dihydroxybiphenyl) and condensed polycyclic dihydric phenols (dihydroxynaphthalene, binaphthol, etc.)] and the like.
Of (b02), from the viewpoint of the heat resistance of (A1) and the moldability described later, bisphenol and condensed polycyclic dihydric phenol are preferred, and bisphenol A is more preferred.

  Among (b), an aliphatic polyether block that is an AO adduct of an aliphatic dihydric alcohol is preferable from the viewpoint of biodegradability.

Mn in (b) is preferably 300 to 5,000, more preferably 1,000 to 3,000, from the viewpoint of antistatic properties and reactivity with (a).
The terminal group of (b) is preferably a hydroxyl group from the viewpoint of reactivity with (a).

  The lower limit of Mn of (A1) is preferably 2,000, more preferably 4,000, particularly preferably 5,000 from the viewpoint of the mechanical properties of the molded product to be described later, and (A1) biodegradable polyester resin (B). From the viewpoint of dispersibility, the upper limit is preferably 60,000, more preferably 40,000, particularly preferably 30,000.

(A1) is, for example, adding a dicarboxylic acid (a04) to a biodegradable aliphatic polyester-forming monomer (a00) and polymerizing the polyester block (a) at 200 ° C. under pressure (0.1 to 1 Mpa). After the production, the polyether chain-containing block (b) can be added thereto and polymerized at a high temperature (160 to 270 ° C.) and under reduced pressure (0.03 to 3 kPa).
In the polyesterification reaction, an esterification catalyst can be used. Examples of the catalyst include an antimony catalyst (such as antimony trioxide) and a tin catalyst (such as monobutyltin oxide).
, Titanium catalysts (tetrabutyl titanate, etc.), zirconium catalysts (tetrabutyl zirconate, etc.) and acetate metal salt catalysts (zinc acetate, zirconyl acetate, etc.).
The amount of the catalyst used is preferably 0.1 to 5%, more preferably 0.2 to 3% based on the total weight of (a) and (b) from the viewpoint of reactivity and mechanical properties of the molded product. It is.
The amount of (b) constituting (A1) is preferably 20 to 90%, more preferably 25 to 80%, from the viewpoint of antistatic properties and mechanical properties of the molded product, based on the weight of (A1). .

[Anionic group-containing block polymer (A2)]
(A2) is a block polymer comprising the polyester block (a) and an anionic group-containing block (c), and is obtained by bonding (a) and (c) alternately and / or randomly.

  The anionic group-containing block (c) contains a dicarboxylic acid having a sulfo group and a diol as essential structural units, and preferably has 2 to 80 (more preferably 3 to 60) sulfo groups in the molecule. An anionic hydrophilic block (c1), a diol having a sulfo group, and a dicarboxylic acid as essential constituent units, and preferably having 2 to 80 (more preferably 3 to 60) sulfo groups in the molecule (Co) polymerization of a vinyl monomer having a hydrophilic block (c2) and a sulfo group by various polymerization methods (for example, radical polymerization method, Ziegler catalyst polymerization method and metallocene catalyst polymerization method), or other vinyl monomers (as described above) And an anionic hydrophilic block (c3) obtained by copolymerization with the.

  Examples of the sulfo group-containing dicarboxylic acid constituting (c1) include sulfo group-containing aromatic and aliphatic dicarboxylic acids.

Examples of the sulfo group-containing aromatic dicarboxylic acid include C8-20, such as 2-, 4- and 5-sulfoisophthalic acid, 4-sulfo-2,6-naphthalenedicarboxylic acid, salts of these sulfo groups only, and esters thereof. Formable derivatives [eg lower alkyl (C1-4) esters (eg methyl esters and ethyl esters) and acid anhydrides] are included.
The sulfo group-containing aliphatic dicarboxylic acid includes C4-18, for example, sulfosuccinic acid, salts of these sulfo groups only, and ester-forming derivatives thereof (same as above).
Examples of the salt of only the sulfo group of the dicarboxylic acid include salts of alkali metals (for example, lithium, sodium and potassium) or alkaline earth metals (for example, calcium and magnesium), ammonium salts, amine (C1 to C30) salts, mono-, Di- and trialkanolamine (C2-6) salts, quaternary ammonium salts of the amine salts and mixtures of two or more thereof.
Of these, aromatic dicarboxylic acids having a sulfo group are preferable from the viewpoint of heat resistance, and 2-, 4- and 5-sulfoisophthalic acid, and 4-sulfo-2,6-naphthalenedicarboxylic acid are more preferable. is there.

Examples of the diol constituting (c1) include AO adducts of alkylene glycol, polyoxyalkylene and a hydroxyl group-containing compound.
Alkylene glycols include C2-C12, such as ethylene glycol, propylene glycol, 1,6-hexanediol and 1,12-dodecanediol.
As polyoxyalkylene (C is 2 to 4 for alkylene, and the addition form may be random and / or block), polymerization degree is 2 to 60, for example, polyoxyethylene (for example, polymerization degree is 2 to 20), polyoxypropylene (Eg, degree of polymerization 2-20) and polyoxyethylene / propylene copolymer (weight ratio 10 / 90-90 / 10) (eg, degree of polymerization 2
30).

  Examples of the hydroxyl group-containing compound constituting the AO adduct of the hydroxyl group-containing compound include alkylene glycol (above) and dihydric phenol (above). The molecular weight of the AO adduct of the hydroxyl group-containing compound is usually Mn 150 to 2,500, and preferably Mn 300 to 2,000 from the viewpoint of heat resistance.

  Among these diols, preferred are C2-10 alkylene glycol, polyoxyethylene having a polymerization degree of 2-20, EO 2-60 mol adduct of bisphenol, and two or more of these from the viewpoint of heat resistance and antistatic properties. Mixtures, more preferred are ethylene glycol and polyoxyethylene (degree of polymerization 6-15), and particularly preferred is an EO 6-20 molar adduct of bisphenol A.

(C1) can be produced, for example, by adding the above diol to a sulfo group-containing dicarboxylic acid and subjecting it to a polycondensation reaction at a high temperature (160 to 270 ° C.) and a reduced pressure (0.03 to 3 kPa). The above-mentioned polyesterification catalyst can be used for the polycondensation reaction, and the amount used is also the same.
The amount of the catalyst used is preferably 0.1 to 5%, more preferably 0.2 to 3%, based on the total weight of the diol and the dicarboxylic acid.

Examples of the sulfo group-containing diol constituting (c2) include AO2 to 10 mol adducts of sulfamic acid.
Examples of the dicarboxylic acid constituting (c2) include the above (a04). (C2) can be produced by the same method as (c1).

Examples of the vinyl monomer containing a sulfo group constituting (c3) include C4-25 unsaturated sulfones and sulfoxides, such as vinylethylsulfone, divinylsulfone and divinylsulfoxide; and C2-25 unsaturated sulfonic acids (salts). ), Eg alkene sulfonic acids [eg vinyl, methyl vinyl, ethyl vinyl, n- and i-propyl vinyl, n-, i-, sec- and t-butyl vinyl and n-amyl vinyl sulfonic acids, and (meth) allyl sulfonic acids ], Unsaturated aromatic sulfonic acids (eg styrene sulfonic acid and α-methyl styrene sulfonic acid), alkenyl and alkyl (C1-18) alkenyl esters of sulfocarboxylic acids (eg α-sulfoalkanoic acid and sulfosuccinic acid) [eg methyl Vinyl, professional Pyr (meth) allyl and stearyl (meth) allylsulfosuccinate, and (meth) allylsulfolaurate], sulfo (hydroxy) alkyl (meth) acrylates and corresponding (meth) acrylamides [eg, sulfoethyl and sulfopropyl (meth) Acrylate, 3- (meth) acryloyloxy-2-hydroxypropanesulfonic acid, 2- (meth) acrylamide-2-methylpropanesulfonic acid and 3- (meth) acrylamide-2-hydroxypropanesulfonic acid] and salts thereof. Can be mentioned.
The salts of these sulfo groups include alkali metal (above) salts, alkaline earth metal (above) salts, ammonium salts, amines [for example, mono-, di- having hydroxyalkyl (C2-4) groups. And triamine] salts, quaternary ammonium salts obtained by quaternizing these amines (salts) with a quaternizing agent (for example, methyl chloride, dimethyl sulfate and benzyl chloride), and mixtures of two or more of these. It is done.

Among these, from the viewpoint of dispersibility in the biodegradable resin (B) described later, alkene sulfonic acid, unsaturated aromatic sulfonic acid and salts thereof are preferable, and ethyl vinyl, n-propyl vinyl and Styrene sulfonic acid and salts thereof, particularly preferred are styrene sulfonic acid and salts thereof.

  Examples of vinyl monomers copolymerizable with sulfo group-containing vinyl monomers include aromatic ring-containing monomers (such as styrene), hydrocarbon vinyl monomers (such as aliphatic hydrocarbons and alicyclic hydrocarbons), acrylic monomers, and other unsaturated monomers. Mono- and dicarboxylic acids and derivatives thereof, carboxylic acid esters of unsaturated alcohols, alkyl ethers of unsaturated alcohols, halogen-containing vinyl monomers and mixtures of two or more thereof (addition form may be random and / or block). ).

  Aliphatic hydrocarbons include olefins [C2-30, such as ethylene, propylene, C4-30 (preferably 4-12, more preferably 4-10) α-olefins (eg 1-butene, 4-methyl-1). -Pentene, 1-pentene, 1-octene, 1-decene and 1-dodecene)] and alkadienes [C4-30 (preferably 4-18, more preferably 4-8) such as butadiene, isoprene and 1,11- Dodecadiene].

  Alicyclic hydrocarbons include cycloalkenes (C5-30, such as cyclopentene, cyclohexene, cycloheptene and cyclooctene) and cycloalkadienes (C5-30, such as cyclopentadiene, 1,3- and 1,4-cyclohexadiene, 1,3- and 1,4-cycloheptadiene, 1,3-, 1,4- and 1,5-cyclooctadiene and 1-methyl-1,4-cyclohexadiene).

Acrylic monomers include C3-30, such as (meth) acrylic acid and derivatives thereof, (meth) acrylonitrile and (meth) acrylamide.
Examples of (meth) acrylic acid derivatives include alkyl (C1-20) (meth) acrylates [eg methyl-, ethyl- and butyl (meth) acrylates] and mono- and di-alkyl (C1-4) aminoalkyl ( C2-4) (meth) acrylates [for example, aminoethyl (meth) acrylate and dimethylaminoethyl (meth) acrylate].

As unsaturated monocarboxylic acid, C4-30 (preferably C4-18, more preferably 4-12), such as crotonic acid, 3,3-dimethylacrylic acid, ethylacrylic acid, 2- and 4-pentenoic acid, 2- and 3-hexenoic acid, 2-methyl-pentenoic acid, 2,2-dimethyl-pentenoic acid, 6-heptenoic acid, 2-ethyl-2-hexenoic acid and 2-octenoic acid, unsaturated dicarboxylic acid, C4-30 (preferably C4-18, more preferably 4-12) unsaturated dicarboxylic acids such as maleic acid, fumaric acid and itaconic acid.
Unsaturated mono- and dicarboxylic acid derivatives include C4-30, such as mono- and dialkyl (C1-20) esters (eg methyl crotonic acid, dimethyl maleate and diethyl itaconate), acid anhydrides (eg maleic anhydride) , Itaconic anhydride) and acid imides (eg maleic imide).

Carboxylic acid esters of unsaturated alcohols include C4-6, such as carboxylic acid (C2-4) esters of unsaturated alcohols [C2-4, eg vinyl alcohol and (meth) allyl alcohol] [eg vinyl acetate and acetic acid (meta ) Allyl], and alkyl ethers of unsaturated alcohols include C3-30, for example alkyl (C1-20) ethers of unsaturated alcohols (same as above).
Halogen-containing vinyl monomers include C2-12, such as vinyl chloride, vinylidene chloride and chloroprene.

(C3) can be produced by various polymerization methods such as bulk polymerization, pearl polymerization, solution polymerization and emulsion polymerization. The polymerization temperature is usually 25 to 250 ° C., preferably 50 to 150 ° C., and the polymerization time is usually 0.5 to 10 hours.

  Examples of the polymerization initiator include azo compounds, peroxides, and mixtures thereof. Of these, preferred are initiators having a functional group, more preferred are azo compounds having a carbonyl group, a hydroxyl group, an amino group, an epoxy group or an isocyanate group, and peroxides having a carbonyl group.

Among the azo compounds having a functional group, those having a carbonyl group include, for example, 3,3-azobis (3-cyanopropionic acid), 4,4′-azobis (4-cyanovaleric acid), 4-tbutylazo- 4-cyanovaleric acid, 4,4′-azobis (4-cyanopentanoic acid), 2,2′-azobis (methylisobutyrate), 1,1′-azobis (1-acetoxy-1-phenylethane) ), 1,1′-azobisformamide and 2-cyano-2-propylazoformamide;
Examples of those having a hydroxyl group include 2,2′-azobis [2- (hydroxymethyl) propionitrile], 2,2′-azobis [2- (hydroxyethyl) propionitrile], 2,2′-. Azobis [2- (hydroxymethyl) butyronitrile], 4,4 azobiscyanopentanol, di- (3-hydroxybutyl) -2,2′azobisisobutyrate and di- (4-hydroxybutyl) -2, 2 'azobisisobutyrate;

Examples of those having an amino group include 2,2′-azobis [2- (aminomethyl) propionitrile], 2,2′-azobis [2- (aminoethyl) propionitrile], 2,2′-. Azobis [2- (aminomethyl) butyronitrile] and 4-acetaminophenyl-azo-triphenylmethane;
Examples of those having an epoxy group include 2,2′-azobis [2- (glycidyloxyethyl) propionitrile] and 2,2′-azobis [2- (glycidyloxyethyl) butyronitrile];
Examples of those having an isocyanate group include 2,2′-azobis [2- (isocyanatoethyl) propionitrile] and 2,2′-azobis [2- (isocyanatoethyl) butyronitrile].

Among the peroxides having a functional group, those having a carbonyl group include, for example, cyclohexanone peroxide, succinic acid peroxide, t-butylperoxymaleic acid, methylcyclohexanone peroxide, t-butylperoxyacetate, cyclopentaneacetyl peroxide. Oxide and cyclohexaneformyl peroxide;
Examples of those having a hydroxyl group include cyclohexanone peroxide;

  Examples of those having an amino group include dimethylaminomethyl-t-amyl peroxide, diethylaminomethyl-t-amyl peroxide, diisopropylaminomethyl-t-amyl peroxide, 1- [4- (dimethylaminophenyl] Examples include ethyl-t-butyl peroxide and 2- [4- (dimethylaminophenyl] propyl-t-butyl peroxide.

As other polymerization initiators other than the initiator having the above functional group, an initiator for styrene (co) polymerization such as 2,2′-azobisisobutyronitrile, 1,1′-azobiscyclohexane 1- Carbonitrile, 2,2'-azobis-4-methoxy-2,4-dimethylvaleronitrile, 2,2'-azobis-2,4-dimethylvaleronitrile, dimethyl-2,2'-azobis (2-methylpro Pionate), 1,1′-azobis (1-acetoxy-1-phenylethane), 2,2′-azobis (4-methoxy-2,4-dimethylvaleronitrile), benzoyl peroxide, di-t-butyl peroxide, cumene hydroperoxide, triethyl boron, diethyl nitrous hydrogen peroxide -Fe (II) salt, persulfate -NaHSO _3, cumene hydroperoxide Fe (II) salt and a lead salt thereof. Of these, 2,2′-azobisisobutyronitrile and 2,2′-azobis-2,4-dimethylvaleronitrile are preferred.

  The Mn of the anionic group-containing block (c) is preferably 300 to 5,000, more preferably 1,000 to 3,000, from the viewpoints of heat resistance and reactivity with the polyester block (a) of (c). is there.

The terminal group (c) is preferably a group containing a carbonyl group (such as a carboxyl group) or a hydroxyl group from the viewpoint of reactivity with the polyester block (a).
The lower limit of Mn of (A2) is preferably 2,000, more preferably 4,000, particularly preferably 5,000 from the viewpoint of the mechanical properties of the molded product to be described later (B2). From the viewpoint of dispersibility, the upper limit is preferably 60,000, more preferably 40,000, particularly preferably 30,000.

  (A2) is prepared by, for example, adding the dicarboxylic acid constituting the above (c2) to a sulfo group-containing diol and polymerizing it at a high temperature (160 to 270 ° C.) under reduced pressure (0.03 to 3 kPa) to produce (c2). And (c2) and the polyester block (a) are polymerized in the same manner as in the production of (c2). The esterification catalyst can be used for the polymerization reaction, and the amount used is preferably 0.1 to 5%, more preferably 0.2 to 3%, based on the total weight of (c2) and (a). is there.

  The amount of (c) constituting (A2) is preferably 20 to 90%, more preferably 25 to 80% based on the weight of (A2) from the viewpoint of antistatic properties and mechanical properties of the molded product. .

[Cationic group-containing block polymer (A3)]
(A3) is a block polymer comprising the polyester block (a) and the cationic group-containing block (d), and is obtained by bonding (a) and (d) alternately and / or randomly.
As (d), a cationic polymer having 2 to 80, preferably 3 to 60, cationic groups separated by a nonionic molecular chain (e) in the molecule can be used.
(E) is selected from the group consisting of divalent hydrocarbon groups; ether bonds, thioether bonds, carbonyl bonds, ester bonds, imino bonds, amide bonds, imide bonds, urethane bonds, urea bonds, carbonate bonds and siloxy bonds. And a divalent organic group having at least one kind of bond; and at least one divalent organic group selected from the group consisting of a divalent organic group having a heterocyclic structure containing a nitrogen atom or an oxygen atom. .

  Of these (e), from the viewpoint of the mechanical properties of the molded article described later, preferred are a divalent hydrocarbon group and a divalent organic group having an ether bond, and more preferred are C2-8 alkylene groups and phenylene groups. And particularly preferred are (poly) oxyalkylene groups, most preferred are (poly) oxyethylene groups and (poly) oxypropylene groups.

Examples of the cationic group include groups having a quaternary ammonium salt or a phosphonium salt. The group having a quaternary ammonium salt is preferably a divalent aliphatic hydrocarbon group containing a quaternary ammonium base from the viewpoint of biodegradability.
As the divalent aliphatic hydrocarbon group containing a quaternary ammonium base, 1, 2 or tertiary amino-alkylene group (for example, aminomethylene group, methylaminoethylene group, dimethylaminoethylene group) was quaternized. Examples include structural groups.

Examples of the counter anion of the cationic group include an anion of a super strong acid having a Hammett acidity function (-H ₀ ) of 12 or more (for example, a proton acid and a combination of a proton acid and a Lewis acid) and other anions.
Examples of super strong acid anions include CF ₃ SO ₃ ⁻ , N (CF ₃ SO ₃ ) ₂ ⁻ , BF ₄ ⁻ , PF ₆ ⁻ , SbF ₆ ⁻ , AsF ₆ ⁻ , TaF ₆ ⁻ , BF ₃ Cl ⁻ and PF. ₅ Cl ⁻ , SbF ₅ Cl ⁻ , AsF ₅ Cl ⁻ , TaF ₅ Cl ⁻ , BF ₃ Br ⁻ , PF ₅ Br ⁻ , SbF ₅ Br ⁻ , AsF ₅ Br ⁻ , TaF ₅ Br ⁻ , BF ₃ I ⁻ , PF ₅ I ⁻ , SbF ₅ I ⁻ , AsF ₅ I ⁻ and TaF ₅ I ⁻ .
Examples of other anions include halogen ions (for example, F ⁻ , Cl ⁻ , Br ⁻ and I ⁻ ), OH ⁻ , PO ₄ ⁻ , alkyl sulfate ions (for example, CH ₃ OSO ₃ ⁻ , C ₂ H ₅ O).
SO ₃ ⁻ and CF ₃ OSO ₃ ⁻ ) and ClO ₄ ⁻ and the anions of aromatic compounds containing a sulfo group [C12-30, such as alkyl (C6-18) benzenesulfonic acid and naphthalenesulfonic acid].

Of these, CF ₃ SO ₃ ⁻ , BF ₄ ⁻ , N (CF ₃ SO ₃ ) ₂ ⁻ , SbF ₆ ⁻ , AsF ₆ ⁻ , TaF are preferable from the viewpoints of heat resistance and antistatic properties of the molded body described later. ₆ ^- and alkyl (C6~18) anion of benzenesulfonic acid and naphthalene sulfonic acid, and more preferred are ^{_{CF 3 SO 3 -, N (}} CF 3 SO 3) 2 -, BF 4 - and alkyl (C6~18) benzene Anions of sulfonic acid and naphthalenesulfonic acid.

  As the production method of (d), for example, an amino group (secondary or tertiary) -containing diol and a quaternizing agent (2 equivalents or 1 equivalent respectively per equivalent of the amino group) are optionally added in the presence of a solvent. A quaternized diol obtained by reacting, or a mixture thereof with a diol before quaternization, and a dicarboxylic acid [or an ester-forming derivative thereof (for example, acid anhydride, lower alkyl ester and acid halide)] A method of reacting polyester with polyester.

  Mn in (d) is preferably 300 to 5,000, more preferably 1,000 to 3,000, from the viewpoints of heat resistance and reactivity with (d) polyester block (a).

  The terminal group of (d) is preferably a group containing a carbonyl group (such as a carboxyl group), a hydroxyl group, an isocyanate group, a thiol group, an epoxy group and / or an amino group from the viewpoint of reactivity with the polyester block (a). It is.

  Mn of (A3) is preferably 2,000, more preferably 4,000, particularly preferably 5,000, (A3) biodegradable polyester resin (B) from the viewpoint of the mechanical properties of the molded product described later. From the viewpoint of dispersibility, the upper limit is preferably 60,000, more preferably 40,000, particularly preferably 30,000.

  (A3) is, for example, adding a dicarboxylic acid to an amino group-containing diol and polymerizing at a high temperature (160 to 270 ° C.) under reduced pressure (0.03 to 3 kPa), and then adding a quaternizing agent and reacting at a high temperature. The cationic group-containing block (d) is produced, and the (d) and the polyester block (a) are polymerized in the same manner as in the production of (d) above. The esterification catalyst can be used for the polymerization reaction, and the amount used is the same as described above.

  The amount of (d) constituting (A3) is preferably 20 to 90%, more preferably 25 to 80% from the viewpoint of antistatic properties and mechanical properties of the molded product based on the weight of (A3). .

Of the polymers (A1), (A2) and (A3) constituting (A), one more preferably selected from the group consisting of (A1) and (A2) is more preferable from the viewpoint of the heat resistance of the molded article described later. Or two or more polymers.

The biodegradable polyester resin (B) in the present invention includes biodegradable polyester resins obtained by a synthesis method and a fermentation method.
Examples of biodegradable polyester resins obtained by synthesis include ring-opening weights of polylactic acid (including D-form, L-form and DL-form) (B-1) and lactones (C3 to 10, γ-butyrolactone, ε-caprolactone, etc.) Compound (B-2) (poly γ-butyrolactone, poly ε-caprolactone, etc.), and polycondensation polymer obtained from dibasic acid and diol (B-3) [polybutylene succinate, polyethylene succinate, and modifications thereof Body (adipate-modified, carbonate-modified or terephthalate-modified polybutylene succinate, etc.)] and a mixture of two or more thereof; and a biodegradable polyester resin by fermentation is polyhydroxybutyrate (B-4). Can be mentioned.

Among the above-mentioned (B), commercially available products for polylactic acid include, for example, Lacia [trade name, manufactured by Mitsui Chemicals, Inc.], lacty [trade name, manufactured by Shimadzu Corporation]; for polycaprolactone, for example, cell green [ Trade name, manufactured by Daicel Chemical Industries, Ltd.]; for polybutylene succinate, for example, Bionore [trade name, manufactured by Showa Polymer Co., Ltd.]; for polyethylene succinate, for example, Lunare SE [trade name, Nippon Shokubai Co., Ltd.] Product]; Examples of polyhydroxybutyrate include Biogreen [trade name, manufactured by Mitsubishi Gas Chemical Co., Ltd.].
Of these (B), (B-1) and / or (B-3) are preferred from the viewpoint of dispersibility of the antistatic agent (A) in (B).

(B) can be produced by any known method. For example, polylactic acid (B-1) can also be prepared by a method in which lactic acid is directly dehydrated and polycondensed, or lactide, which is a cyclic dimer of lactic acid. Examples include a ring polymerization method.
Mn in (B) is preferably 20,000 to 1,000,000, more preferably 50,000 to 500,000, from the viewpoint of mechanical strength and moldability of the molded product. The melting point of (B) is preferably 70 ° C. or higher, more preferably 100 to 200 ° C., and particularly preferably 140 to 180 ° C. from the viewpoint of antistatic properties.

The volume resistivity of the ester group-containing polymer constituting the antistatic agent (A) is 1 × 10 ⁶ to 1 × 10 ¹⁰ Ω · cm, preferably 1 × 10 ⁶ to 1 × 10 ⁹ Ω · cm, more preferably 1 × 10 ⁶ to 1 × 10 ⁸ Ω · cm. When the volume resistivity is less than 1 × 10 ⁶ Ω · cm, the dispersibility of (A) in the biodegradable polyester resin (B) is poor, and when it exceeds 1 × 10 ¹⁰ Ω · cm, the antistatic property of the molded product Becomes worse.

  The ratio of the ester group concentration per unit weight between the ester group-containing polymer constituting (A) and (B) is 0.1 / 1 to 0.9 / 1, preferably 0.3 / 1 to 0.8. / 1. When the ratio of the ester group concentration is less than 0.1 / 1, the biodegradability of the molded product and the dispersibility of (A) in (B) are deteriorated. Becomes worse.

The ester group concentration per unit weight of the ester group-containing polymer constituting (A) is preferably 0.8 to 13.5 mol / kg, more preferably 1.0 to 1.0 from the viewpoint of antistatic properties and biodegradability. 12.5 mol / kg.
The ester group concentration per unit weight of (B) is preferably 8.0 to 15.0 mol / kg, more preferably 11.0 to 14.0 mol / kg, from the viewpoint of biodegradability.

  The antistatic resin composition of the present invention comprises (A) in (B). The proportion of (A) based on the total weight of (A) and (B) can be variously changed according to the required performance, but the lower limit is preferably 1% from the viewpoint of antistatic properties, more preferably 1. From the viewpoint of the mechanical properties of the molded product, the upper limit is preferably 40%, more preferably 30%.

The antistatic resin composition of the present invention includes an alkali metal or alkaline earth metal salt within the range that does not impair the effects of the present invention if necessary, for the purpose of further improving the antistatic property of the resin of the molded product. An additive (C) selected from the group consisting of (C1), surfactant (C2), ionic liquid (C3), compatibilizer (C4) and other additives for resin (C5) may be contained. Good.
The total content of (C1) to (C5) is usually 40% or less based on the total weight of (A) and (B), and the preferable lower limit from the viewpoint of the effect of the additive is 0.001%, more preferably 0. 0.01%, particularly preferably 0.2%, most preferably 0.5%. From the viewpoint of the mechanical properties of the molded product, the upper limit is preferably 30%, more preferably 25%, particularly preferably 20%, most preferably 10. %.

  (C1) may be an organic acid of an alkali metal (for example, lithium, sodium and potassium, the same shall apply hereinafter) or an alkaline earth metal (for example, magnesium and calcium, the same shall apply hereinafter) [for example, C1-12 mono- and dicarboxylic acids (for example formic acid). , Acetic acid, propionic acid, oxalic acid and succinic acid), C1-20 sulfonic acids (eg methanesulfonic acid and p-toluenesulfonic acid) and thiocyanic acid] salts and inorganic acids [eg hydrohalic acids (eg hydrochloric acid and odors) Hydrochloric acid), perchloric acid, sulfuric acid, nitric acid and phosphoric acid] salts.

Specific examples of (C1) include halides [fluorides (lithium fluoride, -sodium, -potassium, -magnesium, -calcium, etc.), chlorides (lithium chloride, -sodium, -potassium, -magnesium, -calcium, etc.) ), Bromides (such as lithium bromide, -sodium, -potassium, -magnesium and -calcium) and iodides (such as lithium iodide, -sodium, -potassium, -magnesium and -calcium)], perchlorates ( Lithium perchlorate, -sodium, -potassium, -magnesium and -calcium), fluorinated sulfonates (lithium fluorosulfonate, -sodium, -potassium, -magnesium and -calcium), methanesulfonate (methane) Lithium sulfonate, -sodium, -ca Um, -magnesium and -calcium), trifluoromethanesulfonate (lithium trifluoromethanesulfonate, -sodium, -potassium, -magnesium and -calcium, etc.), pentafluoroethanesulfonate (lithium pentafluoroethanesulfonate, -Sodium, -potassium, -magnesium and -calcium), nonafluorobutane sulfonate (such as lithium nonafluorobutane sulfonate, -sodium, -potassium, -magnesium and -calcium), undecafluoropentane sulfonate ( Undecafluoropentanesulfonate lithium, -sodium, -potassium, -magnesium, -calcium, etc.), tridecafluorohexanesulfonate (tridecafluorohexanesulfone) Lithium acid, -sodium, -potassium, -magnesium and -calcium), acetate (lithium acetate, -sodium, -potassium, -magnesium and -calcium etc.), sulfate (sodium sulfate, -potassium, -magnesium and- Calcium, etc.), phosphates (sodium phosphate, -potassium, -magnesium, -calcium, etc.), thiocyanates (potassium thiocyanate, etc.) and the like.
Of these, from the viewpoint of antistatic properties, preferred are chloride, perchlorate, trifluoromethanesulfonate, acetate, and more preferred are lithium chloride, -potassium and -sodium, lithium perchlorate, -potassium. And -sodium, lithium trifluoromethanesulfonate, -potassium and -sodium, potassium acetate.

The amount of (C1) used is usually 5% or less based on the total weight of (A) and (B), preferably 0.001 to 0.001 from the viewpoint of good appearance and antistatic properties of the molded product and mechanical properties. It is 3%, more preferably 0.01 to 2.5%, particularly preferably 0.1 to 2%.
As a method of containing (C1), it is preferable to disperse in (A) in advance so as not to impair the transparency of the molded product, and a method of containing (C1) during the production of (A). Further preferred. There is no particular limitation on the timing at which (C1) is contained during the production of (A), and it may be any before, during or after polymerization, but is preferably contained in the raw material before polymerization.

Examples of the surfactant (C2) include nonionic, anionic, cationic and amphoteric surfactants.
Nonionic surfactants include, for example, ethylene oxide addition type nonionic surfactants [for example, higher alcohols (C8-18, the same shall apply hereinafter), higher fatty acids (C8-24, the same shall apply hereinafter) or higher alkylamines (C8-24). ) Ethylene oxide adduct (molecular weight 158 to Mn 200,000); higher fatty acid ester of polyalkylene glycol (molecular weight 150 to Mn 6,000) which is an ethylene oxide adduct of glycol; polyhydric alcohol (C2-18 divalent to octavalent) Or more, such as ethylene glycol, propylene glycol, glycerin, pentaerythritol and sorbitan) higher fatty acid ester ethylene oxide adduct (molecular weight 250-Mn30,000); higher fatty acid amide ethylene oxide adduct (molecular weight 200-M) 30,000); and ethylene oxide adducts of polyhydric alcohols (as described above) alkyl (C3-60) ether (molecular weight 120-Mn30,000)], and polyhydric alcohol (C3-60) type nonionic And surfactants [for example, fatty acid (C3-60) ester of polyhydric alcohol, alkyl (C3-60) ether of polyhydric alcohol and fatty acid (C3-60) alkanolamide].

Examples of the anionic surfactant include compounds other than the above (C1), such as carboxylic acids (for example, C8-22 saturated or unsaturated fatty acids and ether carboxylic acids) or salts thereof; sulfate salts [for example, higher alcohol sulfate salts ( For example, sulfate esters of C8-18 aliphatic alcohols) and higher alkyl ether sulfate esters [eg, sulfate esters of ethylene oxide (1-10 mol) adducts of C8-18 aliphatic alcohols]]; sulfonates [ C10-20, such as alkyl benzene sulfonates (eg sodium dodecylbenzene sulfonate), alkyl sulfonates, alkyl naphthalene sulfonates, dialkyl ester sulfosuccinates, hydrocarbon (eg alkane, α-olefin) sulfonates and Pont T-type]; and phosphate ester salts [e.g. higher alcohol (C8~60) and phosphoric acid ester salts and alkyl ethylene oxide adduct (C4~60) phenol ethylene oxide adduct phosphoric acid ester salt] can be mentioned.
Examples of the salts include alkali metal (for example, lithium, sodium and potassium) salts, alkaline earth metal (for example, calcium and magnesium) salts, ammonium salts, alkylamine (C1-20) salts and alkanolamines (C2-12, For example, mono-, di- and triethanolamine) salts.

  Cationic surfactants include quaternary ammonium salt types [eg, tetraalkyl (C4-100) ammonium salts (eg, lauryltrimethylammonium chloride, didecyldimethylammonium chloride, dioctyldimethylammonium bromide and stearyltrimethylammonium bromide), Alkyl (C3-80) benzylammonium salts (eg lauryldimethylbenzylammonium chloride (benzalkonium chloride), alkyl (C2-60) pyridinium salts (eg cetylpyridinium chloride), polyoxyalkylene (C2-4) trialkylammonium salts (Eg, polyoxyethylenetrimethylammonium chloride) and sapamine type quaternary ammonium salts (eg, stearamide ester) Rudiethylmethyl ammonium methosulfate)]; and amine salt forms [eg higher aliphatic amines (C12-60, eg laurylamine, stearylamine, cetylamine, hardened tallow amine and rosinamine) inorganic acids (eg hydrochloric acid, sulfuric acid, nitric acid and Phosphoric acid) salts or organic acids (C2-22, eg acetic acid, propionic acid, lauric acid, oleic acid, benzoic acid, succinic acid, adipic acid and azelaic acid) salts, ethylene oxide adducts of aliphatic amines (C1-30) Inorganic acids (above) or organic acids (above) and tertiary amines (C3-30, eg triethanolamine monostearate and stearamide ethyl diethyl methylethanolamine) Thing) salt or organic acid (above thing) salt] It is.

  Examples of amphoteric surfactants include amino acid type amphoteric surfactants [for example, higher alkylamine (C8-24) sodium propionate], betaine type amphoteric surfactants [for example, alkyl (C12-18) dimethylbetaine], sulfate ester salts Type amphoteric surfactants [e.g. sulfate sodium salt of higher alkylamine (C8-24) and hydroxyethyl imidazoline sulfate sodium salt], sulfonate type amphoteric surfactants (e.g. pentadecyl sulfotaurine and imidazoline sulfonic acid) and Examples thereof include phosphate ester type amphoteric surfactants [for example, phosphate ester amine salts of glycerin higher fatty acid (C8-24) esterified products].

These (C2) may be used alone or in combination of two or more.
Of these, anionic surfactants are preferred from the viewpoint of heat resistance and antistatic properties of the resin of the molded article, more preferred are sulfonates, and particularly preferred are alkylbenzene sulfonates, alkyl sulfonates and paraffins. Sulfonate.

The amount of (C2) used is usually 15% or less based on the total weight of (A) and (B), and preferably 0.001 to 0.001 from the viewpoint of good appearance and antistatic properties of the molded product and mechanical properties. It is 12%, more preferably 0.01 to 10%, particularly preferably 0.1 to 8%.
The method for containing (C2) is not particularly limited, but it is preferably contained in advance in (A) in order to effectively disperse in the resin composition. When (C2) is previously contained in (A), it is preferably contained during the production (polymerization) of (A), and the timing of inclusion is not particularly limited, and can be any before, during or after polymerization. Although it is good, it is preferably contained in the raw material before polymerization.

  The ionic liquid (C3) is a compound excluding the above (C1) and (C2), has a melting point of room temperature or lower, and at least one of cations or anions constituting (C3) is an organic ion, and has an initial conductivity. Is a room temperature molten salt of 1 to 200 ms / cm (preferably 10 to 200 ms / cm), for example, a room temperature molten salt described in WO95 / 15572. Examples of the cation constituting (C3) include an amidinium cation, a guanidinium cation, and a tertiary ammonium cation.

Examples of the amidinium cation include imidazolinium cation [1,2,3,4-tetramethylimidazolinium, 1,3,4-trimethyl-2-ethylimidazolinium, 1,3-dimethylimidazolinium. 1,3-dimethyl-2,4-diethylimidazolinium, etc.], imidazolium cation [1,3-dimethylimidazolium, 1,3-diethylimidazolium, 1-ethyl-3-methylimidazolium, 1, 2,3-trimethylimidazolium, etc.], tetrahydropyrimidinium cation [1,3-dimethyl-1
, 4,5,6-tetrahydropyrimidinium, 1,2,3-trimethyl-1,4,5,6-tetrahydropyrimidinium, 1,2,3,4-tetramethyl-1,4,5 6-tetrahydropyrimidinium, 1,2,3,5-tetramethyl-1,4,5,6-tetrahydropyrimidinium, etc.], and dihydropyrimidinium cation [1,3-dimethyl-1,4- Or 1,6-dihydropyrimidinium, 1,2,3-trimethyl-1,4- or -1,6-dihydropyrimidinium, 1,2,3,4-tetramethyl-1,4- or -1,6-dihydropyrimidinium and the like].

Examples of the guanidinium cation include a guanidinium cation having an imidazolinium skeleton [2-dimethylamino-1,3,4-trimethylimidazolinium, 2-diethylamino-1,3,4-trimethylimidazolinium, 2-diethylamino-1,3-dimethyl-4-ethylimidazolinium, 2-dimethylamino-1-methyl-3,4-diethylimidazolinium, etc.], guanidinium cation having an imidazolium skeleton [2-dimethyl Amino-1,3,4-trimethylimidazolium, 2-diethylamino-1,3,4-trimethylimidazolium, 2-diethylamino-1,3-dimethyl-4-ethylimidazolium, 2-dimethylamino-1-methyl -3,4-diethylimidazolium etc.], tetrahydropyrimidi Guanidinium cation having a skeleton [2-dimethylamino-1,3,4-trimethyl-1,4,5,6-tetrahydropyrimidinium, 2-diethylamino-1,3,4-trimethyl-1,4 , 5,6-tetrahydropyrimidinium, 2-diethylamino-1,3-dimethyl-4-ethyl-1,4,5,6-tetrahydropyrimidinium, etc.], and guanidinium having a dihydropyrimidinium skeleton Cation [2-dimethylamino-1,3,4-trimethyl-1,4- or -1,6-dihydropyrimidinium, 2-diethylamino-1,3,4-trimethyl-1,4- or -1, 6-dihydropyrimidinium, 2-diethylamino-1,3-dimethyl-4-ethyl-1,4- or -1,6-dihydropyrimidinium Etc.], and the like.

  Examples of the tertiary ammonium cation include methyl dilauryl ammonium.

The amidinium cation, guanidinium cation and tertiary ammonium cation may be used alone or in combination of two or more.
Of these, from the viewpoint of initial conductivity, an amidinium cation is preferable, an imidazolium cation is more preferable, and a 1-ethyl-3-methylimidazolium cation is particularly preferable.

In the ionic liquid (C3), examples of the organic acid or inorganic acid constituting the anion include the following.
Examples of the organic acid include carboxylic acid, sulfuric acid ester, higher alkyl ether sulfuric acid ester, sulfonic acid and phosphoric acid ester. For example, the organic acid described in (C2) and (C4) described later may be used. it can.
Examples of the inorganic acid include super strong acids (for example, borofluoric acid, tetrafluoroboric acid, perchloric acid, hexafluorophosphoric acid, hexafluoroantimonic acid and hexafluoroarsenic acid), phosphoric acid and boric acid. It is done.
The organic acid and inorganic acid may be used alone or in combination of two or more.
Among the organic and inorganic acids, are preferred from the viewpoint of the initial conductivity of the (C3) is anionic Hamett acidity function constituting the (C3) (-H ₀₎ is 12 to 100, the superacid conjugate base , Acids that form anions other than the conjugate bases of super strong acids and mixtures thereof.

  Examples of the anion other than the conjugate base of the super strong acid include halogen (for example, fluorine, chlorine and bromine) ions, alkyl (C1-12) benzenesulfonic acid (for example, p-toluenesulfonic acid and dodecylbenzenesulfonic acid) ions and poly (n = 1-25) Fluoroalkanesulfonic acid (for example, undecafluoropentanesulfonic acid) ion.

Super strong acids include those derived from protonic acids and combinations of protonic acids and Lewis acids, and mixtures thereof.
Examples of the protonic acid as the super strong acid include bis (trifluoromethylsulfonyl) imidic acid, bis (pentafluoroethylsulfonyl) imidic acid, tris (trifluoromethylsulfonyl) methane, perchloric acid, fluorosulfonic acid, alkane (C1 -30) sulfonic acid [eg methane sulfonic acid, dodecane sulfonic acid etc.], poly (n = 1-30) fluoroalkane (C1-30) sulfonic acid (eg trifluoromethane sulfonic acid, pentafluoroethane sulfonic acid, heptafluoropropane) Sulfonic acid, nonafluorobutanesulfonic acid, undecafluoropentanesulfonic acid and tridecafluorohexanesulfonic acid), borofluoric acid and tetrafluoroboric acid.
Of these, borofluoric acid, trifluoromethanesulfonic acid and bis (pentafluoroethylsulfonyl) imidic acid are preferred from the viewpoint of ease of synthesis.

Examples of the protonic acid used in combination with the Lewis acid include hydrogen halide (for example, hydrogen fluoride, hydrogen chloride, hydrogen bromide and hydrogen iodide), perchloric acid, fluorosulfonic acid, methanesulfonic acid, trifluoromethanesulfonic acid. , Pentafluoroethanesulfonic acid, nonafluorobutanesulfonic acid, undecafluoropentanesulfonic acid, tridecafluorohexanesulfonic acid and mixtures thereof.
Of these, hydrogen fluoride is preferred from the viewpoint of the initial conductivity of (C3).

Examples of the Lewis acid include boron trifluoride, phosphorus pentafluoride, antimony pentafluoride, arsenic pentafluoride, tantalum pentafluoride, and mixtures thereof.
Of these, boron trifluoride and phosphorus pentafluoride are preferable from the viewpoint of the initial conductivity of (C3).
The combination of the protonic acid and the Lewis acid is arbitrary, but as the super strong acid comprising these combinations, for example, tetrafluoroboric acid, hexafluorophosphoric acid, hexafluorotantalic acid, hexafluoroantimonic acid, tantalum hexafluoride Examples include sulfonic acid, tetrafluoroboric acid, hexafluorophosphoric acid, chloroboron trifluoride, arsenic hexafluoride, and mixtures thereof.

  Of the above anions, (C3) from the viewpoint of the initial conductivity, a super strong acid conjugate base (a super strong acid composed of a proton acid and a super strong acid composed of a combination of a proton acid and a Lewis acid), more preferably It is a conjugate base of a super strong acid consisting of a super strong acid consisting of a proton acid and a proton acid and boron trifluoride and / or phosphorus pentafluoride.

The amount of (C3) used is usually 10% or less based on the total weight of (A) and (B), preferably from 0.001 in view of the good appearance and antistatic effect of the molded product and mechanical properties. 5%, more preferably 0.01 to 3%.
The method for adding (C3) is not particularly limited, but from the viewpoint of effective dispersion in the resin, it is preferable to disperse in (A) in advance, and after the production (polymerization) of (A). More preferably, (C3) is added and dispersed in advance.

  As the production method of (C3), for example, an dimethyl carbonate salt of an amidinium cation and / or a guanidinium cation obtained by quaternization with dimethyl carbonate or the like, an acid [the above organic acid constituting an anion in (C3) Or an inorganic acid] to perform acid exchange, or after hydrolyzing the amidinium cation and / or guanidinium cation to form a monoamidoamine, the monoamidoamine is converted to an acid (same as above). The method of neutralizing is mentioned.

As the compatibilizing agent (C4), for example, a modified vinyl (co) polymer having at least one polar group selected from the group consisting of a carboxyl group, an epoxy group, an amino group, a hydroxyl group and a polyoxyalkylene group (for example, a special compound) And a modified vinyl (co) polymer having a sulfo group (for example, those described in JP-A-6-345927) and a polyolefin portion and an aromatic vinyl polymer portion. Examples thereof include block (co) polymers (for example, those described in JP-A-6-345927).
The amount of (C4) used is usually 15% or less based on the total weight of (A) and (B), preferably from the viewpoint of the compatibility of (A) and (B) and the mechanical properties of the molded product. It is 1 to 12%, more preferably 1 to 10%, particularly preferably 1.5 to 8%.

  Other additives for resin (C5) include conductive substance (C51), colorant (C52), filler (C53), nucleating agent (C54), lubricant (C55), plasticizer (C56), flame retardant (C57), dispersant (C58), mold release agent (C59), antioxidant (C510), ultraviolet absorber (C511) and antibacterial agent (C512).

  The conductive substance (C51) is a compound other than the above (C1) and (C3), and examples thereof include carbon nanotubes, carbon black, and white carbon.

Examples of the colorant (C52) include inorganic pigments, organic pigments, and dyes.
Examples of inorganic pigments include white pigments (eg, titanium oxide, lithopone, lead white and zinc white), cobalt compounds (eg, aureoline, cobalt green, cerulean blue, cobalt blue and cobalt violet), and iron compounds (eg, iron oxide and bitumen). , Chromium compounds (eg chromium oxide, lead chromate and barium chromate) and sulfides (eg cadmium sulfide, cadmium yellow and ultramarine).
Examples of organic pigments include azo pigments (eg, azo lake, monoazo, disazo, and chelate azo) and polycyclic pigments (eg, benzimidazolone, phthalocyanine, quinacridone, dioxazine, isoindolinone, thioindigo). Perylene, quinophthalone, and anthraquinone).
Examples of the dye include azo, anthraquinone, indigoid, sulfide, triphenylmethane, pyrazolone, stilbene, diphenylmethane, xanthene, alizarin, acridine, quinoneimine, thiazole, methine, nitro System, nitroso system and aniline system.

  Examples of the filler (C53) include inorganic fillers (eg, calcium carbonate, talc, clay, silicic acid, silicate, asbestos, mica, glass fiber, glass balloon, carbon fiber, metal fiber, ceramic whisker and titanium whisker). And organic fillers [for example, urea, calcium stearate and organic crosslinked fine particles (for example, epoxy-based and urethane-based)].

  Examples of the nucleating agent (C54) include organic nucleating agents [for example, 1,3,2,4-dibenzylidene-sorbitol, aluminum-mono-hydroxy-di-pt-butylbenzoate, sodium bis (4-t -Butylphenyl) phosphate and sodium benzoate] and inorganic nucleating agents (eg graphite, carbon black, magnesium oxide, calcium silicate, magnesium silicate, talc, kaolin, calcium carbonate, magnesium carbonate, sodium carbonate, potassium carbonate, zinc oxide, Alumina, barium sulfate and calcium sulfate).

  Lubricants (C55) include waxes (eg carnauba wax, paraffin wax and polyolefin wax), higher fatty acids (C8-24, eg stearic acid, oleic acid, linoleic acid and linolenic acid), higher alcohols (C8-18, eg stearyl). Alcohols, lauryl alcohol, myristyl alcohol, cetyl alcohol, cetostearyl alcohol and behenyl alcohol) and higher fatty acid amides (C8-24, such as stearic acid amide, oleic acid amide, linoleic acid amide and linolenic acid amide).

  Examples of the plasticizer (C56) include aromatic carboxylic acid esters [for example, phthalic acid esters (for example, dioctyl phthalate and dibutyl phthalate)], aliphatic monocarboxylic acid esters [for example, methyl acetyl ricinoleate and triethylene glycol dibenzoate], aliphatic Dicarboxylic acid esters [for example, di (2-ethylhexyl) adipate and adipic acid-propylene glycol-based polyester (Mn 200 to 2000)], aliphatic tricarboxylic acid esters [for example, citric acid ester (for example, triethyl citrate)], phosphoric acid triesters [ For example, triphenyl phosphate] and petroleum resin.

  Examples of the flame retardant (C57) include organic flame retardants [for example, nitrogen-containing [for example, urea compounds, guanidine compounds, and triazine compounds (for example, melamine and guanamine) salts (for example, inorganic acid (the foregoing) salts, cyanurates and isocyanates)]. Nurates)], sulfur-containing systems (eg sulfates, organic sulfonic acids, sulfamic acids, organic sulfamic acids, and their salts, esters and amides), silicon-containing systems (eg polyorganosiloxanes) and phosphorus-containing systems [eg Phosphate esters (eg tricresyl phosphate)]] and inorganic flame retardants (eg antimony trioxide, magnesium hydroxide, zinc borate, barium metaborate, aluminum hydroxide, red phosphorus and ammonium polyphosphate).

Examples of the dispersant (C58) include dispersants of Mn 1,000 to 100,000, such as naphthalene sulfonic acid formalin condensate (Mn 1,000 to 10,000), polystyrene sulfonate metals [for example, alkali metals (for example, sodium and potassium) ] Salt (Mn 1,000-100,000), polyacrylic acid metal [for example, alkali metal (same as above)] salt (Mn 2,000-50,000), carboxymethyl cellulose and polyvinyl alcohol.

  As the release agent (C59), lower fatty acid (C1-4) alcohol ester (for example, butyl stearate) of higher fatty acid (above), polyvalent (divalent to tetravalent or higher) of fatty acid (C2-18) ) Alcohol esters (eg hydrogenated castor oil), glycol (C2-8) esters of fatty acids (C2-18) (eg ethylene glycol monostearate) and liquid paraffin. Tetrakis [methylene- (3,5-di-tert-butyl-4-hydroxyhydrocinnamate)] methane

  Antioxidants (C510) include phenolic {eg monocyclic phenols [eg 2,6-di-t-butyl-p-cresol and butylated hydroxyanisole], bisphenols [eg 2,2′-methylenebis (4- Methyl-6-tert-butylphenol), 4,4′-butylidenebis (3-methyl) -6-tert-butylphenol and 4,4′-thiobis (3-methyl) -6-tert-butylphenol] and polycyclic phenols [ For example, 1,3,5-trimethyl-2,4,6-tris (3,5-di-tert-butyl-4-hydroxybenzyl) benzene, 1,1,3-tris (2-methyl-4-hydroxy-) 5-t-butylphenyl) butane and tetrakis [methylene- (3,5-di-t-butyl-4-hydroxyhydrocinnamate)] Product name: Irganox 1010, manufactured by Ciba Specialty Chemicals Co., Ltd.]]; sulfur-based [eg, dilauryl 3,3′-thiodipropionate, distearyl 3,3′-thiodipropionate, lauryl stearyl 3, 3′-thiodipropionate, dimyristyl 3,3′-thiodipropionate, distearyl β, β′-thiodibutyrate and dilauryl sulfide]; phosphorus systems [eg triphenyl phosphite, triisodecyl phosphite, Diphenylisodecyl phosphite, phenyl diisodecyl phosphite, tris (2,4-di-tert-butylphenyl) phosphite, 2,2-methylenebis (4,6-di-tert-butylphenyl) octyl phosphite, 4, 4′-butylidene-bis (3-methyl-6-tert-butylphenol Luditridecyl) phosphite, cyclic neopentanetetrayl bis (octadecyl phosphite), cyclic neopentanetetrayl bis (2,6-di-t-butyl-4-methylphenyl) phosphite, cyclic neopentanetetrayl Bis (2,4-di-t-butylphenyl) phosphite and diisodecylpentaerythritol diphosphite]; and amine systems such as octylated diphenylamine, Nn-butyl-p-aminophenol, N, N-diisopropyl- p-phenylenediamine, N, N-bis (1-ethyl-3-methylpentyl) -p-phenylenediamine, N, N-diphenyl-p-phenylenediamine, N-phenyl-α-naphthylamine, phenyl-β-naphthylamine And phenothia Down], and the like.

  Examples of the ultraviolet absorber (C511) include benzotriazoles [for example, 2- (2′-hydroxy-5′-methylphenyl) benzotriazole and 2- (2′-hydroxy-4′-octoxyphenyl) benzotriazole], Benzophenone series [eg 2-hydroxy-4-methoxybenzophenone and 2,2′-dihydroxy-4-methoxybenzophenone], salicylate series [eg phenyl salicylate and ethylene glycol monosalicylate] and acrylate series [eg 2-ethylhexyl 2-cyano-3,3′1-diphenyl acrylate].

As an antibacterial agent (C512), benzoic acid, paraoxybenzoic acid ester, sorbic acid, halogenated phenol (for example, 2,4,6-tribromophenol sodium salt), organic iodine (for example, 4-chlorophenyl-3-iodopropargyl) Formal), nitrile (eg, 2,4,5,6-tetrachloroisophthalonitrile), thiocyano (eg, methylene bisthianocyanate), N-haloalkylthioimide (eg, N-tetrachloroethyl-thio-tetrahydrophthalimide), copper agent (Eg 8-oxyquinoline copper), benzimidazole (eg 2-4-thiazolylbenzimidazole), benzothiazole (eg 2-thiocyanomethylthiobenzothiazole), trihaloallyl (eg 3-bromo-2,3-diiodo- 2-prop Ruethyl carbonate), triazoles (eg azaconazole), organic nitrogen sulfur compounds (eg Suraoff 39), quaternary ammonium compounds (eg trimethoxysilyl-propyloctadecyl ammonium chloride) and pyridine-based compounds [eg 2, 3, 5, 6 -Cytochloro-4- (methylsulfonyl) -pyridine].

  The amount of (C5) used is usually 20% or less in the whole (C5) based on the total weight of (A) and (B), and (C53), (C56), (C57), (C58) and (C512) are usually 10% or less, preferably 1 to 5%; (C51) and (C52) are usually 5% or less, preferably 0.1 to 3%; (C54) and (C55 ), (C59), (C510) and (C511) are usually 2% or less, preferably 0.01 to 0.5%.

As the method for producing the resin composition of the present invention, (A) and (B), or (C) is added to these as necessary [[C1] to (C4) are effective as described above. From the viewpoint of dispersion, it may be previously contained in (A). The method of melt-mixing is mentioned.
As a method of melt mixing, for example, a method of mixing pellets or powdery components with an appropriate mixer (for example, a Henschel mixer) and then melt-mixing (150 to 260 ° C.) with an extruder to pelletize. It is done.
The order of addition of each component during mixing is not particularly limited. For example, (1) (A) and (B), or a method in which (C) is added all at once as necessary to blend and knead And (2) A method of blending and kneading a part of (A) and (B) or, if necessary, (C) and kneading the remaining (C).
Among these methods, the method (2) is called a master batch method or a master pellet method, and is a preferable method from the viewpoint of uniformly dispersing a small amount of (C) in a resin.

  Examples of the molding method of the resin composition of the present invention include injection molding, compression molding, calendar molding, slush molding, rotational molding, extrusion molding, blow molding and film molding (for example, casting method, tenter method and inflation method). Any method can be selected according to the purpose.

The molded product made of the resin composition of the present invention has excellent mechanical strength and permanent antistatic properties, and also has good paintability and printability, and is molded by coating and / or printing the molded product. An article is obtained.
Examples of the method for coating the molded product include, but are not limited to, air spray coating, airless spray coating, electrostatic spray coating, immersion coating, roller coating, and brush coating.
Examples of the paint include paints generally used for plastic coating such as polyester melamine resin paint, epoxy melamine resin paint, acrylic melamine resin paint, and acrylic urethane resin paint.
The coating film thickness (dry film thickness) can be appropriately selected according to the purpose, but is usually 10 to 50 μm.

In addition, as a method of printing after coating the molded product or the molded product, any printing method generally used for plastic printing can be used. For example, gravure printing, flexographic printing , Screen printing, pad printing, dry offset printing, offset printing, and the like.
As the printing ink, those usually used for printing plastics, for example, gravure ink, flexographic ink, screen ink, pad ink, dry offset ink and offset ink can be used.

  EXAMPLES The present invention will be specifically described below with reference to examples, but the present invention is not limited to these examples. In addition, the part in an Example represents a weight part.

Production Example 1
In a stainless steel autoclave, 94.8 parts of L-lactide having an optical purity of 99% or more, 5 parts of adipic acid, antioxidant [trade name: Irganox 1010, manufactured by Ciba Specialty Chemicals Co., Ltd., and so on. ] 0.3 parts and 6 parts of water were charged, the inside of the autoclave was purged with nitrogen, and then heated and stirred at 220 ° C. under pressure (0.3 to 0.5 MPa) for 4 hours under sealed conditions. Acid value having carboxyl groups at both ends 100 parts of 78 polyesters (a-1) were obtained.
Next, 68.5 parts of polyethylene glycol of Mn 2,000 and 1.5 parts of zirconyl acetate were added and polymerized at 245 ° C. under reduced pressure of 0.13 kPa or less for 5 hours to form a viscous polyether chain-containing block polymer (A1 ) The antistatic agent (A-1) consisting of (A1) was obtained by taking out (A1) in a strand form on a belt and pelletizing it. The volume resistivity of the block polymer (A1) was 5 × 10 ⁸ Ω · cm, the ester group concentration per unit weight was 7.8 mol / kg, and Mn was 10,500.

Production Example 2
A stainless steel autoclave is charged with 41 parts of adipic acid, 59 parts of sodium salt of sulfamic acid diethanol and 0.5 part of zirconyl acetate, heated to 220 ° C. over 2 hours and reduced to 1 mmHg over 1 hour for polyesterification reaction. An anionic polymer (c-1) having an average of 8 sodium sulfonate bases in one molecule was obtained.
Next, 50 parts of (c-1), 50 parts of (a-1), and 0.5 parts of zirconyl acetate were charged into another stainless steel autoclave, and the anionic group-containing block polymer (A2) was prepared in the same manner as in Production Example 1. An antistatic agent (A-2) comprising The volume resistivity of the block polymer (A2) was 1 × 10 ⁸ Ω · cm, the ester group concentration per unit weight was 9.4 mol / kg, and Mn was 10,300.

Production Example 3
A stainless steel autoclave was charged with 48 parts of N-methyldiethanolamine, 52 parts of adipic acid and 0.5 part of zirconyl acetate, heated to 220 ° C. over 2 hours, and reduced to 1 mmHg over 1 hour to conduct a polyesterification reaction. . After completion of the reaction, 100 parts of methanol was added to the product and dissolved. While stirring, the temperature in the autoclave was kept at 120 ° C., 33 parts of dimethyl carbonate was gradually added dropwise over 3 hours, and aged at the same temperature for 6 hours. After cooling to room temperature, 100 parts of a 60% hexafluorophosphoric acid aqueous solution was added and stirred at room temperature for 1 hour. Subsequently, the solvent was distilled off under reduced pressure to obtain a cationic polymer (d-1) having an average of 10 quaternary ammonium bases in the molecule.
Next, another stainless steel autoclave was charged with 50 parts of (d-1), 50 parts of (a-1) and 0.5 part of zirconyl acetate, and thereafter the cationic group-containing block polymer (A3) in the same manner as in Production Example 1. An antistatic agent (A-3) comprising The volume resistivity of the block polymer (A3) was 8 × 10 ⁷ Ω · cm, the ester group concentration per unit weight was 10.1 mol / kg, and Mn was 13,000.

Production Example 4
A stainless steel autoclave was charged with 69.9 parts of L-lactide having an optical purity of 99% or more, 29.9 parts of adipic acid, 0.3 part of an antioxidant and 6 parts of water. The mixture was heated and stirred for 4 hours under pressure (0.3 to 0.5 MPa) and sealed to obtain 100 parts of polyester (a-2) having an acid value of 230 having carboxyl groups at both ends.
Next, 1,643 parts of polyethylene glycol of Mn 8,000 and 15.5 parts of zirconyl acetate were added, and an antistatic agent (ratio A-) comprising a polyether chain-containing block polymer (ratio A1) in the same manner as in Production Example 1 below. 1) was obtained. The volume resistivity of the block polymer (ratio A1) was 5 × 10 ⁸ Ω · cm, the ester group concentration per unit weight was 0.6 mol / kg, and Mn was 11,000.

Examples 1-7, Comparative Examples 1-3
According to the formulation shown in Table 1, the antistatic agent and the biodegradable resin [described later (B-1), (B-2)], or an additive (C) is further added to these and added for 3 minutes with a Henschel mixer. After blending, the resin composition (Examples 1-7, Comparative Examples 1-3) was melt-kneaded at 200 ° C. under a condition of a rotational speed of 100 rpm and a residence time of 3 minutes in a twin-screw extruder with a vent. Obtained.

(B-1): Polylactic acid [Brand name: Lacty 1012, manufactured by Shimadzu Corporation, ester group concentration per unit weight of 13.9 mol / kg]
(B-2): Polybutylene succinate [Brand name: Bionore # 1003, Showa Polymer Co., Ltd.
Manufactured by Co., Ltd., ester group concentration per unit weight 13.2 mol / kg]
(C-1): sodium dodecylbenzenesulfonate (C-2): sodium lauryl phosphate (C-3): lithium trifluoromethanesulfonate (C-4): 1-ethyl-3-methylimidazolium trifluoromethanesulfone Naruto

(performance test)
About the said resin composition, each uses injection molding machine [PS40E5ASE, the Nissei Plastic Industry Co., Ltd.], predetermined | prescribed cylinder temperature [(B-1) containing resin composition is 200 degreeC, and mold temperature is 50 degreeC, respectively. Molded articles were prepared, and the antistatic property, biodegradability and dispersibility were evaluated according to the following methods. The results are shown in Table 2.

[1] Antistatic property (1) Volume specific resistance value Using a test piece (100 × 100 × 2 mm), a super insulation meter [DSM-8103 manufactured by Toa Denpa Kogyo Co., Ltd. (electrode SME-8310 for flat plate sample), the same. ] In an atmosphere of 23 ° C. and humidity 50% RH (according to ASTM D257).
(2) Volume resistivity value after water washing The surface of the test piece (100 × 100 × 2 mm) leaning diagonally was washed with 100 ml of ion-exchanged water (23 ° C.) at a flow rate of 100 ml / min, and then in a circulating dryer 80 Dry at 3 ° C. for 3 hours. About the test piece which repeated this water washing-drying operation 10 times, the volume specific resistance value was measured by 23 degreeC and humidity 50% RH atmosphere by the super insulation meter similarly to (1) (based on ASTM D257).

[2] Biodegradability A test piece (100 × 100 × 2 mm) was buried in soil at a depth of about 20 cm from the ground surface, and the appearance change after 6 months was visually observed and evaluated according to the following criteria.
○: Change in appearance (molded piece does not retain its original shape due to biodegradation)
×: No change in appearance

[3] Dispersibility When the molded product was bent 180 °, the fracture surface was visually observed, and the dispersibility of the antistatic agent in the biodegradable resin was evaluated according to the following criteria. In the following, delamination means interfacial delamination between the layer of the antistatic agent (A) and the biodegradable polyester resin (B).

○: Dispersibility is good without delamination ×: Delamination is recognized and dispersibility is poor

  As is apparent from Table 2, the molded article of the present invention is superior in all of antistatic properties, biodegradability and dispersibility, and is superior to the molded article of the comparative example.

  The antistatic agent of the present invention can impart excellent permanent antistatic properties without impairing the biodegradability of the biodegradable resin, and is excellent in dispersibility. A molded product obtained by molding a resin composition containing the antistatic agent in the biodegradable resin has excellent biodegradability and excellent permanent antistatic properties. From this, the antistatic resin composition of the present invention can be used for injection molding, compression molding, calendar molding, slush molding, rotational molding, extrusion molding, blow molding and film molding (for example, casting method, tenter method and inflation method), etc. Housing products such as home appliances / OA equipment, game machines and office equipment, various plastic containers such as IC trays, various packaging films, flooring sheets, artificial turf, mats and automobile parts It can be widely used as a material for various molded articles such as.

Claims (7)

^{1 × 10 6 ~1 × 10 10} Ω · cm in volume resistivity an ester group-containing polymer having an antistatic agent (A), containing a biodegradable polyester resin (B) and ionic liquid (C3) The ratio of the ester group concentration per unit weight between the polymer and (B) [(mol / kg) / (mol / kg)] is 0.1 / 1 to 0.9 / 1. An antistatic biodegradable resin composition. The composition according to claim 1, wherein the ester group concentration per unit weight of the ester group-containing polymer is 0.8 to 13.5 mol / kg. The ester group-containing polymer is one or more polymers selected from the group consisting of a polyether chain-containing block polymer (A1), an anionic group-containing block polymer (A2), and a cationic group-containing block polymer (A3). The composition according to claim 1 or 2. The composition according to any one of claims 1 to 3, wherein the proportion of (A) is 1 to 40% based on the total weight of (A) and (B). It consists of an ester group-containing polymer having a volume resistivity of 1 × 10 ⁶ to 1 × 10 ¹⁰ Ω · cm, and the ratio of the ester group concentration per unit weight between the polymer and the biodegradable polyester resin (B) is 0 The antistatic agent (A) for a composition according to any one of claims 1 to 4 , which is: 1/1 to 0.9 / 1 [(mol / kg) / (mol / kg)] . Claim 1 by molding the composition according to any one of the 4 antistatic resin molded products. A molded article obtained by coating and / or printing the molded article according to claim 6 .