JP5882712B2 - Polylactic acid resin composition and resin molded body thereof - Google Patents

Description

  The present invention relates to a polylactic acid resin composition and a resin molded body thereof.

In the face of problems such as depletion of petroleum resources and CO ₂ reduction, polylactic acid using lactic acid obtained by fermenting grain resources such as corn as a raw material has attracted attention. Polylactic acid is a plant-derived resin as described above, and has the property of being highly rigid and excellent in transparency, but because it cannot be used under high temperature conditions due to low heat resistance and impact resistance, Its use is limited compared to ordinary resins.

  As a method for improving the heat resistance of polylactic acid, for example, there is a method of increasing the crystallization degree by heat treatment (annealing treatment). However, the heat treatment time is very long and impractical, and the transparency increases with the progress of crystallization. There are problems such as lowering.

  Therefore, in recent years, as a method for solving these problems, various plasticizers and crystal nucleating agents have been studied in a resin composition containing polylactic acid as a polymer.

  For example, it has been proposed to use a fatty acid ester comprising a sugar alcohol dehydration condensate and a fatty acid as the plasticizer, and a layered silicate as the crystal nucleating agent (Patent Document 1).

  In addition, for example, it has been proposed to use a saturated ester as the plasticizer and use an aliphatic ester or a fatty acid amide as the crystal nucleating agent (Patent Document 2).

WO2008 / 010318 JP 2007-130895 A

  However, the resin composition disclosed in Patent Document 1 has a low heat resistance, and the usable applications are very limited. In addition, the resin composition is prone to deformation when the molded product is removed unless the molding time is long, so that the productivity at the time of molding the mold is poor. is there.

  On the other hand, although the resin composition disclosed in Patent Document 2 has slightly improved impact resistance, it is easy to elute into water and alcohol, and a molded product having excellent impact resistance and dissolution resistance is obtained. I can't. Furthermore, since the resin composition does not have sufficient productivity at the time of mold molding, there is still room for improvement.

  The present invention has been made in view of such circumstances, and is a polylactic acid resin composition that is excellent in impact resistance, elution resistance, and heat resistance, and is excellent in productivity during mold molding, and a resin molded body thereof. The purpose is to provide

In order to achieve the above object, the first gist of the present invention is a polylactic acid resin composition containing the following components (B) to (D) together with the following component (A).
(A) Polylactic acid.
(B) A reaction product of at least one of a polyol and a polyol dehydration condensate, an alkylene oxide mainly composed of ethylene oxide, and a fatty acid having 12 to 24 carbon atoms.
(C) Fatty acid amide.
(D) Silica compound.

  Moreover, this invention makes the 2nd summary the resin molding which consists of a polylactic acid resin composition of said 1st summary.

  That is, the present inventors have conducted extensive research in order to obtain a polylactic acid resin composition that is excellent in impact resistance, elution resistance, and heat resistance, and also excellent in productivity at the time of mold molding. As a result, in the resin composition containing polylactic acid as a polymer, a specific reaction product as a plasticizer, that is, at least one of a polyol and a polyol dehydration condensate, an alkylene oxide mainly composed of ethylene oxide, and a carbon number of 12 Formulation of reaction products (component B) with 24 to 24 fatty acids, a fatty acid amide (component C) as a crystal nucleating agent, and a silica compound (component D) to further improve impact resistance, etc. Then, the present inventors have found that the intended purpose can be achieved, and have reached the present invention.

  As described above, the polylactic acid resin composition of the present invention comprises polylactic acid (component A), at least one of a polyol and a polyol dehydration condensate, an alkylene oxide mainly composed of ethylene oxide, and a fatty acid having 12 to 24 carbon atoms. And a reaction product (component B), a fatty acid amide (component C), and a silica compound (component D). Therefore, it has excellent impact resistance, elution resistance, and heat resistance, and also exhibits excellent effects on productivity at the time of mold molding (resin can be efficiently efficiently in a short time without causing deformation at the time of demolding). To obtain a molded body). Moreover, since it is excellent in heat resistance etc., there exists an effect that the high temperature countermeasure at the time of transportation is unnecessary, for example.

  In particular, when the reaction product as component B contains an oxyethylene group in a specific range, the polylactic acid resin composition of the present invention and the resin molded product thereof are excellent in transparency, productivity during molding, and the like. become.

  Furthermore, the polylactic acid resin composition of the present invention is such that the polyol which is the material of the reaction product of the component B is a specific polyol such as glycerin, erythritol, pentaerythritol, xylitol, sorbitol, mannitol, galactitol, maltitol And the resin molding becomes more excellent in impact resistance and the like.

  In addition, when the fatty acid amide as the C component is a bisamide compound obtained by reacting a fatty acid having 8 to 24 carbon atoms having a hydroxyl group with a compound having two amino groups, the polylactic acid resin composition of the present invention And the resin molding becomes more excellent in transparency etc.

  In addition, when the content of the reaction product as the component B is in a specific range, the polylactic acid resin composition of the present invention and the resin molded body thereof are more excellent in impact resistance and the like.

  Furthermore, when the content of the fatty acid amide as the C component is in a specific range, the polylactic acid resin composition of the present invention and the resin molded body thereof are more excellent in productivity at the time of molding.

In addition, when the content of the silica (SiO ₂ ) component (in the component D) is in a specific range, the polylactic acid resin composition and the resin molded body thereof according to the present invention have more impact resistance, crystallization speed, etc. To become better.

  Next, modes for carrying out the present invention will be specifically described, but the present invention is not limited to these.

As described above, the polylactic acid resin composition of the present invention has at least one of polyol and polyol dehydration condensate, an alkylene oxide mainly composed of ethylene oxide, and 12 to 12 carbon atoms, together with polylactic acid (component A). It contains a reaction product (component B) with 24 fatty acids, a fatty acid amide (component C), and a silica compound (component D). In the polylactic acid resin composition of the present invention, the reaction product of the component (B) usually has a function as a plasticizer, and the fatty acid amide of the component (C) has a function as a crystal nucleating agent. . In addition to the above components, the polylactic acid resin composition of the present invention contains other resins, other inorganic fillers, hydrolysis inhibitors, impact resistance improvers, antioxidants, and the like as necessary. be able to.
Hereinafter, these will be described.

[Polylactic acid]
The polylactic acid (component A) in the polylactic acid resin composition of the present invention is a polylactic acid obtained by polycondensation of only lactic acid as a raw material monomer, or a lactic acid component and a hydroxycarboxylic acid component other than lactic acid (hereinafter referred to as a raw material monomer). And also referred to as a hydroxycarboxylic acid component) and polylactic acid obtained by condensation polymerization.

  In lactic acid, there are optical isomers of L-lactic acid (L form) and D-lactic acid (D form). In the present invention, either or both of the optical isomers may be contained as the lactic acid component, but both the flexibility, rigidity and heat resistance of the polylactic acid resin composition, and production at the time of molding From the viewpoint of safety, it is preferable to use lactic acid having high optical purity mainly composed of any optical isomer. In the present specification, the “main component” refers to a component whose content in the lactic acid component is 80 mol% or more.

  The content of the L-form or D-form in the lactic acid component when only the lactic acid component is polycondensed, that is, the content of the larger of the isomers is 95.0 mol% or more from the above viewpoint. It is preferable that it is 98 mol% or more.

  The content of the L-form or D-form in the lactic acid component when the lactic acid component and the hydroxycarboxylic acid component are subjected to polycondensation, that is, the higher content of the isomers is 95.0 from the above viewpoint. It is preferably at least mol%, more preferably at least 98 mol%.

  In addition, the polylactic acid is composed mainly of polycondensation of D form as lactic acid, polycondensation of L form only as lactic acid, copolymer of D form and L form, and other main components. A blend of L-form polylactic acid and D-form polylactic acid at an arbitrary ratio may be used.

  On the other hand, examples of the hydroxycarboxylic acid component other than lactic acid include hydroxycarboxylic acid compounds such as glycolic acid, hydroxybutyric acid, hydroxyvaleric acid, hydroxypentanoic acid, hydroxycaproic acid, and hydroxyheptanoic acid. These are used together. Of these, glycolic acid and hydroxycaproic acid are preferable.

  Moreover, in this invention, the dimer of the said lactic acid and the hydroxycarboxylic acid compound may be contained in each component. For example, lactide, which is a cyclic dimer of lactic acid, is used as the dimer of lactic acid, and glycolide, which is a cyclic dimer of glycolic acid, is used as the dimer of the hydroxycarboxylic acid compound, for example. The lactide includes L-lactide, which is a cyclic dimer of L-lactic acid, D-lactide, which is a cyclic dimer of D-lactic acid, meso-lactide obtained by cyclic dimerization of D-lactic acid and L-lactic acid, DL-lactide, which is a racemic mixture of D-lactide and L-lactide, and any lactide can be used in the present invention, but the flexibility and rigidity of the polylactic acid resin composition and the polylactic acid resin From the viewpoint of productivity during molding, D-lactide and L-lactide are preferred. In addition, the dimer of lactic acid may be contained in the lactic acid component in any case where only the lactic acid component is polycondensed and in the case where the lactic acid component and the hydroxycarboxylic acid component are polycondensed.

  The condensation polymerization reaction of only the lactic acid component and the condensation polymerization reaction of the lactic acid component and the hydroxycarboxylic acid component are not particularly limited and can be performed using a known method.

  The weight average molecular weight of the polylactic acid in the present invention is usually in the range of 10,000 to 400,000, preferably in the range of 50,000 to 400,000, and more preferably in the range of 100,000 to 300,000. That is, if the weight average molecular weight of the polylactic acid is less than the above range, the mechanical properties of the resin molded product are low, and conversely, if the weight average molecular weight of the polylactic acid exceeds the above range, the fluidity during molding may be poor. Because it becomes. The polylactic acid has a weight average molecular weight of gel permeation chromatograph (GPC), chloroform as the solvent, high-temperature SEC column (GMHHR-H series) manufactured by Tosoh Corporation, flow rate 1.0 mL / min, column temperature 40 It can be obtained by conversion using ° C, a differential refractive index detector (RI) as a detector, and styrene having a known molecular weight as a reference.

[Plasticizer]
The plasticizer in the polylactic acid resin composition of the present invention includes a reaction product (component B) of at least one of a polyol and a polyol dehydration condensate, an alkylene oxide mainly composed of ethylene oxide, and a fatty acid having 12 to 24 carbon atoms. ) Is used. The above “alkylene oxide mainly composed of ethylene oxide” means that a majority of the alkylene oxide is ethylene oxide, and includes the fact that all of the alkylene oxide is ethylene oxide. In addition, when things other than ethylene oxide are used together with ethylene oxide as said alkylene oxide, for example, propylene oxide, butylene oxide, isobutylene oxide, etc. are used together.

  The polyol that is a material of the reaction product of the component (B) is not particularly limited, but preferably from the viewpoint of impact resistance and the like, glycerin, erythritol, pentaerythritol, xylitol, sorbitol, mannitol, gas Lactitol, maltitol, etc. are used.

  As a method for producing the reaction product (component B), for example, polyol and polyol dehydration condensate and fatty acid are reacted under heating to esterify the polyol and polyol dehydration condensate, and further ethylene in an autoclave under heating. Examples thereof include a method in which an oxide is subjected to an addition reaction to obtain the reaction product (component B). Moreover, after adding an ethylene oxide to a polyol and a polyol dehydration condensate, you may make a fatty acid react. In addition, a fatty acid ester is synthesized in advance with a fatty acid and a monohydric alcohol (methanol, ethanol) having a short carbon number, subjected to a transesterification reaction with a polyol and a polyol dehydration condensate, and ethylene oxide is added in the same manner as in the above method. There is also a method for obtaining a reaction product (component B). The reaction product (component B) thus obtained is used alone or in combination of two or more in the polylactic acid resin composition of the present invention.

  From the viewpoint of excellent impact resistance in the polylactic acid resin composition of the present invention, the content ratio of the oxyethylene group in the reaction product (component B) is preferably 20 to 95% by weight, more preferably 30. ~ 95 wt%.

  The reaction product (component B) may be either a saturated ester in which all the hydroxyl groups of the polyol and the polyol dehydration condensate are esterified with fatty acids, or a partial ester in which a part of the hydroxyl groups is esterified.

  From the viewpoint of impact resistance, the reaction product (component B) preferably has an average of 2 or more (greater than 2) 9 or less ester groups in the molecule, and more than 2.5 (from 2.5 Large) It is more preferable to have 6 or less.

  From the viewpoint of excellent impact resistance and elution resistance to water and alcohol solvents in the polylactic acid resin composition of the present invention, fatty acids having 12 to 24 carbon atoms are used for the synthesis of the reaction product (component B), Preferably, a fatty acid having 14 to 24 carbon atoms is used. That is, when the number of carbon atoms in the fatty acid is less than the above range, desired impact resistance is difficult to obtain, and the amount of elution into water and alcohol solvents increases. Conversely, when the number of carbon atoms in the fatty acid exceeds the above range, compatibility is poor and transparency is poor. In addition, the said fatty acid may use what corresponds to either saturated or unsaturated, and may use them further together. Moreover, the mixture of the fatty acid converted from fats and oils may be sufficient, and the thing whose average carbon number is the said range is used in that case.

  And as said reaction product (B component), specifically, polyoxyethylene glycerol laurate, polyoxyethylene glycerol cocoate, polyoxyethylene glycerol myristate, polyoxyethylene glycerol palmitate, polyoxyethylene glycerol Linoleate, polyoxyethylene glyceryl stearate, polyoxyethylene glycerin isostearate, polyoxyethylene glycerin-12-hydroxystearate, polyoxyethylene glycerin oleate, polyoxyethylene glycerin eicosinate, polyoxyethylene glycerin behenate , Polyoxyethylene glycerine lignoserate, polyoxyethylene erythritol laurate, polyoxyethylene erythritol cocoate, poly Xylethylene erythritol myristate, polyoxyethylene erythritol palmitate, polyoxyethylene erythritol linoleate, polyoxyethylene erythritol stearate, polyoxyethylene erythritol isostearate, polyoxyethylene erythritol-12-hydroxystearate, polyoxy Ethylene erythritol oleate, polyoxyethylene erythritol eicosanate, polyoxyethylene erythritol behenate, polyoxyethylene erythritol lignocerate, polyoxyethylene anhydroerythritol laurate, polyoxyethylene anhydroerythritol cocoate, polyoxyethylene anhydro Erythritol myristylate, polyoxyethylene Droerythritol palmitate, polyoxyethylene anhydroerythritol linoleate, polyoxyethylene anhydroerythritol stearate, polyoxyethylene anhydroerythritol isostearate, polyoxyethylene anhydroerythritol-12-hydroxystearate, polyoxyethylene anhydro Erythritol oleate, polyoxyethylene anhydroerythritol eicosinate, polyoxyethylene anhydroerythritol behenate, polyoxyethylene anhydroerythritol lignoserate, polyoxyethylene sorbitol laurate, polyoxyethylene sorbitol cocoate, polyoxyethylene sorbitol Myristylate, polyoxyethylene sorbitol palmi Tate, polyoxyethylene sorbitol linoleate, polyoxyethylene sorbitol stearate, polyoxyethylene sorbitol isostearate, polyoxyethylene sorbitol-12-hydroxystearate, polyoxyethylene sorbitol oleate, polyoxyethylene sorbitol eicosinate, Polyoxyethylene sorbitol behenate, polyoxyethylene sorbitol lignoserate, polyoxyethylene sorbitan laurate, polyoxyethylene sorbitan cocoate, polyoxyethylene sorbitan myristate, polyoxyethylene sorbitan palmitate, polyoxyethylene sorbitan linoleate, polyoxy Ethylene sorbitan stearate, polyoxyethylene sorbitans isotea , Polyoxyethylene sorbitans-12-hydroxytearate, polyoxyethylene sorbitan oleate, polyoxyethylene sorbitan eicosanate, polyoxyethylene sorbitan behenate, polyoxyethylene sorbitan lignocerate, polyoxyethylene isosorbide laurate Rate, polyoxyethylene isosorbide cocoate, polyoxyethylene isosorbide myristate, polyoxyethylene isosorbide palmitate, polyoxyethylene isosorbide linoleate, polyoxyethylene isosorbide stearate, polyoxy Ethylene isosorbide isostearate, polyoxyethylene isosorbide-12-hydroxystearate, polyoxyethylene isosorbide oleate, poly Xylethylene isosorbide eicosanate, polyoxyethylene isosorbide behenate, polyoxyethylene isosorbide gnoselate, polyoxyethylene mannitol laurate, polyoxyethylene mannitol cocoate, polyoxyethylene mannitol myristate, poly Oxyethylene mannitol palmitate, polyoxyethylene mannitol linoleate, polyoxyethylene mannitol stearate, polyoxyethylene mannitol isostearate, polyoxyethylene mannitol-12-hydroxystearate, polyoxyethylene mannitol oleate, polyoxyethylene mannitol eico Sanate, polyoxyethylene mannitol behenate, polyoxyethylene mannitol rig Noserato, polyoxyethylene mannitan laurate, polyoxyethylene mannitan cocoate, polyoxyethylene mannitan myristate, polyoxyethylene mannitan palmitate, polyoxyethylene mannitan linoleate, polyoxyethylene mannitan stearate , Polyoxyethylene mannitan isostearate, polyoxyethylene mannitan-12-hydroxystearate, polyoxyethylene mannitan oleate, polyoxyethylene mannitan eicosinate, polyoxyethylene mannitan behenate, polyoxyethylene mannitan Lignocerate, polyoxyethylene isomannide laurate, polyoxyethylene mannide cocoate, polyoxyethylene mannide myristate, polio Siethylene mannide palmitate, polyoxyethylene mannidonolate, polyoxyethylene mannide stearate, polyoxyethylene mannide isostearate, polyoxyethylene mannide-12-hydroxystearate, polyoxyethylene mannide oleate , Polyoxyethylene mannide laurate, polyoxyethylene mannide eicosinate, polyoxyethylene mannide behenate, polyoxyethylene mannide lignoselate, polyoxyethylene xylitol laurate, polyoxyethylene xylitol cocoate, polyoxy Ethylene xylitol myristate, polyoxyethylene xylitol palmitate, polyoxyethylene xylitol linoleate, polyoxyethylene key Ritol stearate, polyoxyethylene xylitol isostearate, polyoxyethylene xylitol-12-hydroxystearate, polyoxyethylene xylitol oleate, polyoxyethylene xylitol eicosinate, polyoxyethylene xylitol behenate, polyoxyethylene xylitol Lignoserato, polyoxyethylene anhydroxylitol laurate, polyoxyethylene anhydroxylitol cocoate, polyoxyethylene anhydroxylitol myristylate, polyoxyethylene anhydroxylitol palmitate, polyoxyethylene anhydroxylitol linoleate, poly Oxyethylene anhydroxylitol stearate, polyoxyethylene anhydroxylitol Ruisostearate, polyoxyethylene anhydroxylitol-12-hydroxystearate, polyoxyethylene anhydroxylitol oleate, polyoxyethylene anhydroxylitol eicosinate, polyoxyethylene anhydroxylitol behenate, polyoxyethylene an Hydroxylitol lignoselate, polyoxyethylene maltitol laurate, polyoxyethylene maltitol cocoate, polyoxyethylene maltitol myristate, polyoxyethylene maltitol palmitate, polyoxyethylene maltitol linoleate, polyoxyethylene multi Tall stearate, polyoxyethylene maltitol isostearate, polyoxyethylene maltitol-12-hydroxys Allate, polyoxyethylene maltitol oleate, polyoxyethylene maltitol eicosanate, polyoxyethylene maltitol behenate, polyoxyethylene maltitol lignoserate, polyoxyethylene anhydro maltitol laurate, polyoxyethylene anhydro Maltitol cocoate, polyoxyethylene anhydro maltitol myristate, polyoxyethylene anhydro maltitol palmitate, polyoxyethylene anhydro maltitol linoleate, polyoxyethylene anhydro maltitol stearate, polyoxyethylene an Hydromaltitol isostearate, polyoxyethylene anhydromaltitol-12-hydroxystearate, polyoxye Ren anhydro maltitol oleate, polyoxyethylene anhydro maltitol eicosinate, polyoxyethylene anhydro maltitol behenate, polyoxyethylene anhydro maltitol lignocerate, polyoxyethylene galactitol laurate, polyoxyethylene Galactitol cocoate, polyoxyethylene galactitol myristate, polyoxyethylene galactitol palmitate, polyoxyethylene galactitol linoleate, polyoxyethylene galactitol stearate, polyoxyethylene galactitol isostearate, polyoxyethylene Galactitol-12-hydroxystearate, polyoxyethylene galactitol oleate, polyoxyethylene galacti Tall eicosinate, polyoxyethylene galactitol behenate, polyoxyethylene galactitol lignoselate, polyoxyethylene anhydrogalactitol laurate, polyoxyethylene anhydrogalactitol cocoate, polyoxyethylene anhydrogalactitol myristate Rate, polyoxyethylene anhydrogalactitol palmitate, polyoxyethylene anhydrogalactitol linoleate, polyoxyethylene anhydrogalactitol stearate, polyoxyethylene anhydrogalactitol isostearate, polyoxyethylene anhydrogalactitol -12-hydroxystearate, polyoxyethylene anhydrogalactitol oleate, polyoxyethylene Emissions en Hydro galactitol eicosapentaenoic sulfonate, polyoxyethylene en Hydro-galactopyranoside Tito behenate, polyoxyethylene en Hydro galactitol lignocerate, and the like. These may be used alone or in combination of two or more. In addition, since one or more fatty acid ester groups are present in one molecule of the reaction product listed above, for example, the polyoxyethylene glycerol laurate is “polyoxyethylene glycerol monolaurate, polyoxyethylene glycerol dilaurate, Including “polyoxyethylene glycerol trilaurate”.

  The content of the reaction product (component B) in the polylactic acid resin composition of the present invention is 100 parts by weight of polylactic acid (component A) from the viewpoint of excellent impact resistance, productivity during molding, and the like. The amount is preferably 2 to 15 parts by weight, more preferably 3 to 15 parts by weight.

[Crystal nucleating agent]
As the crystal nucleating agent in the polylactic acid resin composition of the present invention, a fatty acid amide (C component) is used from the viewpoint of moldability, heat resistance, impact resistance and the like of the polylactic acid resin molded body.

  The fatty acid amide (C component) used in the present invention may have a hydroxyl group or may not have a hydroxyl group.

  The fatty acid amide having no hydroxyl group is not particularly limited, but is preferably caprylic acid amide, capric acid amide, myristic acid amide, palmitic acid amide because of its excellent impact resistance in the polylactic acid resin composition of the present invention. , Fatty acid monoamides such as lauric acid amide, stearic acid amide, arachidinamide, behenic acid amide, lignoceric acid amide, stearic acid monoethanolamide, oleic acid amide, linoleic acid amide, arachidonic acid amide, ethylene biscaprylic acid amide, butylene Biscaprylic amide, hexamethylene biscaprylic amide, m-xylylene biscaprylic amide, ethylene biscapric amide, butylene biscapric amide, hexamethylene biscapric amide, m-xylylene biscapric acid Amide, ethylene bis lauric acid amide, butylene bis lauric acid amide, hexamethylene bis lauric acid amide, m-xylylene bis lauric acid amide, ethylene bis stearic acid amide, butylene bis stearic acid amide, hexamethylene bis stearic acid amide, m -Xylylene bis stearic acid amide, ethylene bis arachidic acid amide, butylene bis arachidic acid amide, hexamethylene bis arachidic acid amide, m-xylylene bis arachidic acid amide, ethylene bis behenic acid amide, butylene bis behenic acid Amide, hexamethylene bisbehenate amide, m-xylylene bisbehenate amide, ethylene bislignoceramide, butylene bisoleic acid amide, hexamethylene bislignoceramide, m-xylylene bis Gnoceric acid amide, ethylene bis oleic acid amide, butylene bis oleic acid amide, hexamethylene bis oleic acid amide, m-xylylene bis oleic acid amide, ethylene bis linoleic acid amide, butylene bis linoleic acid amide, hexamethylene bis linoleic acid amide And fatty acid bisamides such as m-xylylene bis arachidonic acid amide, ethylene bis arachidonic acid amide, butylene bis arachidonic acid amide, hexamethylene bis arachidonic acid amide, and m-xylylene bis arachidonic acid amide. In addition, these are used individually or in combination of 2 or more types.

  In addition, the fatty acid amide having a hydroxyl group has excellent transparency and the like in the polylactic acid resin composition of the present invention, and thus has, for example, a fatty acid having 8 to 24 carbon atoms having a hydroxyl group and two amino groups. A bisamide compound obtained by reacting a compound is preferably used. In addition, the said fatty acid may use what corresponds to either saturated or unsaturated, and may use them further together. Moreover, the mixture of the fatty acid converted from fats and oils may be sufficient, and the thing whose average carbon number is the said range is used in that case.

  As the fatty acid amide having a hydroxyl group, specifically, 8-hydroxycaprylic acid amide, 10-hydroxylauric acid amide, 10-hydroxycapric acid amide, 11-hydroxymyristic acid amide, 16-hydroxypalmitic acid amide, 12-hydroxystearic acid amide, 2-hydroxyarachidic acid amide, 2-hydroxybehenic acid amide, 2-hydroxylignoceric acid amide, 12-hydroxystearic acid monoethanolamide, 12-hydroxyoleic acid amide, 11-hydroxylinol Hydroxyl-containing fatty acid monoamides such as acid amides and 2-hydroxyarachidonic acid amides, N, N′-ethylenebis-8-hydroxycapric acid amides, N, N′-butylenebis-8-hydroxycapric acid amides, N, '-Hexamethylenebis-8-hydroxycapric acid amide, N, N'-m-xylylenebis-8-hydroxycapric acid amide, N, N'-ethylenebis-10-hydroxylauric acid amide, N, N'-butylenebis -10-hydroxylauric acid amide, N, N′-hexamethylenebis-10-hydroxylauric acid amide, N, N′-m-xylylene bis-10-hydroxylauric acid amide, N, N′-ethylenebis-11 Hydroxymyristic acid amide, N, N′-butylenebis-11-hydroxymyristic acid amide, N, N′-hexamethylenebis-11-hydroxymyristic acid amide, N, N′-m-xylylenebis-11-hydroxymyristic acid amide N, N'-ethylenebis-16-hydroxypalmitin Amide, N, N′-butylenebis-16-hydroxypalmitic acid amide, N, N′-hexamethylenebis-16-hydroxypalmitic acid amide, N, N′-m-xylylenebis-16-hydroxypalmitic acid amide, N, N′-ethylenebis-12-hydroxystearic acid amide, N, N′-butylene bis-12-hydroxystearic acid amide, N, N′-hexamethylene bis-12-stearic acid amide, N, N′-m-xylylene bis -12-hydroxystearic amide, N, N'-ethylenebis-2-hydroxyarachidic acid amide, N, N'-butylene bis-2-hydroxyarachidic acid amide, N, N'-hexamethylene bis-2- Hydroxy arachidic acid amide, N, N'-m-xylylene bis-2-hydroxy Arachidic acid amide, N, N′-ethylenebis-2-hydroxybehenic acid amide, N, N′-butylene bis-2-hydroxybehenic acid amide, N, N′-hexamethylenebis-2-hydroxybehenic acid amide, N , N′-m-xylylene bis-2-hydroxybehenic acid amide, N, N′-ethylene bis-2-hydroxy lignoceric acid amide, N, N′-butylene bis-2-hydroxy lignoceric acid amide, N, N ′ -Hexamethylenebis-2-hydroxylignoceramide, N, N'-m-xylylenebis-2-hydroxylignoceramide, N, N'-ethylenebis-12-hydroxyoleate, N, N'- Butylenebis-12-hydroxyoleic acid amide, N, N′-hexamethylenebis-12-hydroxyoleamide Acid amide, N, N′-m-xylylenebis-12-hydroxyoleic acid amide, N, N′-ethylenebis-11-hydroxylinoleic acid amide, N, N′-butylenebis-11-hydroxylinoleic acid amide, N , N′-hexamethylenebis-11-hydroxylinoleic acid amide, N, N′-m-xylylenebis-11-hydroxylinoleic acid amide, N, N′-ethylenebis-11-hydroxyarachidonic acid amide, N, N ′ Hydroxyl group-containing fatty acid bisamides such as -butylenebis-11-hydroxyarachidonic acid amide, N, N'-hexamethylenebis-11-hydroxyarachidonic acid amide, N, N'-m-xylylenebis-11-hydroxyarachidonic acid amide It is done. These may be used alone or in combination of two or more.

  The content of fatty acid amide (component C) in the polylactic acid resin composition of the present invention is in the range of 0.1 to 0.7 parts by weight with respect to 100 parts by weight of polylactic acid (component A). It is preferable from the viewpoint of improving the productivity at the time.

[Silica compound]
In the polylactic acid resin composition of the present invention, a silica compound (component D) is blended together with the components (A) to (C) from the viewpoint of impact resistance, crystallization speed and the like.

  Examples of the silica compound include silica obtained by the decomposition of silicon halide, dry silica obtained by heating and reducing silica sand and then oxidizing with air, and sodium silicate as a mineral acid such as sulfuric acid. Wet silica obtained by direct decomposition, etc., sol-gel silica obtained by hydrolysis of alkoxysilane, those silicas surface-treated with a silane coupling agent, etc., lactic acid, lactide and polymers thereof And silica compounds obtained by reacting alkoxides with silicon alkoxide compounds. That is, the silica compound is intended to include silica itself, and the shape thereof is not particularly limited, and is in the form of powder, particles, flakes, plates, fibers, needles, cloths, mats, or any other shape. It may be. In addition, the said various silica compounds are used individually or in combination of 2 or more types.

  Examples of the silane coupling agent used for the surface treatment of silica include vinyltrialkoxysilane, N- (2-aminoethyl) 3-aminopropylmethyl dialkoxysilane, and N- (2-aminoethyl) 3-amino. Propyltrialkoxysilane, 3-aminopropyltrialkoxysilane, 3-glycidoxypropyltrialkoxysilane, 3-glycidoxypropylmethyl dialkoxysilane, 2- (3,4-epoxycyclohexyl) ethyltrialkoxysilane 3-chloropropylmethyl dialkoxysilane, 3-chloropropyltrialkoxysilane, 3-methacryloxypropyltrialkoxysilane, 3-mercaptopropyltrialkoxysilane, 3-isocyanatopropyltriethoxysilane, bis (trie Silyl propyl) tetrasulfide, and the like.

  Examples of a method for synthesizing a silica compound obtained by reacting lactic acid, lactide and a polymer thereof with a silicon alkoxide compound include, for example, dehydration polymerization of lactic acid and / or ring-opening polymerization of lactide in the presence of the silicon alkoxide compound. Known methods described in International Publication WO 2007/40187 and the like can be used.

  Examples of the silicon alkoxide compound include tetraalkoxysilane having 1 to 5 carbon atoms in an alkoxy group such as tetraethoxysilane, methyltrialkoxysilane such as methyltriethoxysilane, phenyltrialkoxysilane such as phenyltriethoxysilane, Dimethyl dialkoxysilanes such as dimethyldiethoxysilane, diphenyldialkoxysilanes such as diphenyldimethoxysilane and diphenylsilanediol, vinyltrialkoxysilanes, N- (2-aminoethyl) 3-aminopropylmethyl dialkoxysilanes, N- ( 2-aminoethyl) 3-aminopropyltrialkoxysilane, 3-aminopropyltrialkoxysilane, 3-glycidoxypropyltrialkoxysilane, 3-glycidoxypropylmethyl dial Xysilane, 2- (3,4-epoxycyclohexyl) ethyltrialkoxysilane, 3-chloropropylmethyl dialkoxysilane, 3-chloropropyltrialkoxysilane, 3-methacryloxypropyltrialkoxysilane, 3-mercaptopropyltri Alkoxysilane, N- (1,3-dimethylbutylidene) -3- (trialkoxysilyl) -1-propanamine, N- [2- (vinylbenzylamino) ethyl] -3-aminopropyltrialkoxysilane / hydrochloric acid Salt, N, N′-bis [3- (trialkoxysilyl) propyl] ethylenediamine, oligomer of amino silane coupling agent, oligomer of epoxy silane coupling agent, terminal hydrogenated polydimethylsiloxane, terminal vinylated polydimethyl Siloxane, terminal Tacryloxy-based polydimethylpolysiloxane, terminally hydroxylated polydimethylsiloxane, terminally epoxidized polydimethylsiloxane, terminally carboxylated polydimethylsiloxane, polymethylsilsesquioxane, 90% methyl-10% of polymethyl-hydridosilsesquioxane-10% Hydride, polyphenylsilsesquioxane, 90% phenyl-10% methyl of polyphenyl-methylsilsesquioxane, 70% phenyl-30% dimethyl of phenylsilsesquioxane-dimethylsiloxane copolymer, polyphenyl-propylsilsesquioxane Oxane 70% phenyl, 30% propyl, polyphenyl-vinylsilsesquioxane 90% phenyl-10% vinyl, polycyclohexylsilsesquioxane silanol reactivity> 90% T7 cube, poly Recyclohexyl Silsesquioxane Silanol Reactivity> 95% T7 Cube, Polycyclopentyl Silsesquioxane (H Substitution) T8 Cube for Hydrosilylation, Polycyclopentyl Silsesquioxane (Methacryloxy Substitution) Polymerizable T8 Cube, Polycyclopentyl Examples thereof include polysilsesquioxanes such as silsesquioxane (all H-substituted) T8 cube, poly (2-chloroethyl) silsesquioxane, T8 cube, poly (2-chloroethyl) silsesquioxane, and the like.

Then, the amount of the silica compound of the polylactic acid resin composition of the present invention (D component), impact resistance, from the viewpoint of crystallization rate, the content of the silica (SiO ₂₎ component, polylactic acid ( It is preferable to mix | blend so that it may become the range of 0.01-2 weight part with respect to 100 weight part of A component), and it is more preferable to mix | blend so that it may become the range of 0.01-1 weight part.

[Other resins]
In the polylactic acid resin composition of the present invention, in addition to the above components (A) to (D), the range in which the effects of the present invention are not impaired (less than 20% by weight of the entire polylactic acid resin composition. Preferably 1 to 15). In the range of% by weight, more preferably in the range of 1 to 10% by weight.), Other resins may be appropriately contained. Examples of other resins include thermoplastic resins such as acrylic resin, polypropylene, polystyrene, ABS resin, AS resin, polyphenylene sulfide, polyether ether ketone, polyester, polyacetal, polysulfone, polyphenylene oxide, and polyetherimide, and phenol resin. , Thermosetting resins such as melamine resin, unsaturated polyester resin, silicone resin and epoxy resin. These may be used alone or in combination of two or more. Of these, acrylic resins are preferable from the viewpoint of excellent impact resistance and the like.

[Inorganic filler]
Moreover, the polylactic acid resin composition of the present invention may contain an inorganic filler as necessary. Specific examples of the inorganic filler include talc, clay, mica, zeolite, bentonite, montmorillonite, glass fiber, and carbon fiber. These may be used alone or in combination of two or more.

  From the viewpoint of being excellent in impact resistance, crystallization speed, etc., the content of the inorganic filler (including the silica component of component D) in the polylactic acid resin composition of the present invention is polylactic acid (component A). ) It is preferably in the range of 0.01 to 2 parts by weight, more preferably in the range of 0.01 to 1 part by weight with respect to 100 parts by weight.

(Hydrolysis inhibitor)
Moreover, the hydrolysis inhibitor may contain in the polylactic acid resin composition of this invention as needed. Examples of the hydrolysis inhibitor include carbodiimide compounds such as polycarbodiimide compounds and monocarbodiimide compounds, and polycarbodiimide compounds are preferred from the viewpoint of moldability of polylactic acid resin molded articles, and heat resistance and molding of polylactic acid resin molded articles. Monocarbodiimide compounds are more preferred from the viewpoints of heat resistance, fluidity, impact resistance, and bloom resistance of crystal nucleating agents.

  Examples of the polycarbodiimide compound include poly (4,4′-diphenylmethanecarbodiimide), poly (4,4′-dicyclohexylmethanecarbodiimide), poly (1,3,5-triisopropylbenzene) polycarbodiimide, poly (1,3,3). 5-triisopropylbenzene and 1,5-diisopropylbenzene) polycarbodiimide and the like, and examples of the monocarbodiimide compound include N, N′-di-2,6-diisopropylphenylcarbodiimide and the like.

  And from a viewpoint of the moldability of a polylactic acid resin molded object, content of the hydrolysis inhibitor in the polylactic acid resin composition of this invention is 0.05-2 with respect to 100 weight part of polylactic acid (A component). It is preferably in the range of parts by weight, more preferably in the range of 0.1 to 1 part by weight.

[Impact resistance improver]
Moreover, the polylactic acid resin composition of the present invention may contain an impact resistance improver, if necessary, from the viewpoint of improving physical properties such as flexibility. Examples of the impact resistance improver include (meth) acrylic acid polymer, ethylene- (meth) acrylic acid copolymer, ethylene (meth) acrylic acid alkyl ester copolymer, epoxy-modified silicone acrylic rubber, diene and vinyl monomer. A copolymer with a monomer, a hydrogenated product thereof, an organic fiber such as an aromatic polyamide fiber, a diene rubber, a compatibilizing agent and the like can be used. In addition, (meth) acrylic acid represents acrylic acid and / or methacrylic acid.

  From the viewpoint of impact resistance and moldability of the resin composition, the content of the impact resistance improver in the polylactic acid resin composition of the present invention is 1 to 100 parts by weight of polylactic acid (component A). The range is preferably 20 parts by weight, more preferably 3 to 10 parts by weight.

  The polylactic acid resin composition of the present invention includes, as components other than those described above, a flame retardant, an antioxidant, a lubricant, an antistatic agent, an antifogging agent, a light stabilizer, an ultraviolet absorber, a pigment, a colorant, and an antifungal agent. An agent, an antibacterial agent, a foaming agent, and the like can be contained as long as the object of the present invention is not hindered.

[Preparation of polylactic acid resin composition and resin molding thereof]
The polylactic acid resin composition of the present invention comprises polylactic acid (component A), a specific reaction product (component B) as a plasticizer, a fatty acid amide (component C) as a crystal nucleating agent, and a silica compound (D Ingredients) and other materials as necessary may be blended at a predetermined ratio and melt mixed at 160 to 240 ° C. The melt mixing may be performed after the above materials are blended, and polylactic acid (component A) is first melted using an extruder, a Banbury mixer, a kneader, a heating roll, or the like. Then, other materials may be blended and prepared in the form of pellets.

  A resin molded body can be obtained by casting, injection molding, blow molding, extrusion molding, or the like using the resin composition melt-mixed as described above as a material. Moreover, it can also be set as various molded objects by shaping | molding methods, such as vacuum forming after a sheet process, pressure forming, and vacuum pressure forming.

  When molding using the mold when obtaining the resin molded body, the mold temperature during the molding is preferably 40 to 140 ° C, more preferably 70 to 120 ° C, from the viewpoint of productivity. Range. Moreover, the holding time in the metal mold | die of the said resin molding in vacuum forming, pressure forming, and vacuum pressure forming is 1-15 second from viewpoints of productivity etc., More preferably, it is 1-10 second.

  Further, the polylactic acid resin molded body of the present invention was measured for elution amount according to the elution test method defined by the FCN system related to food packaging containers of the US FDA, and the cumulative estimated daily intake (CEDI) was calculated. The smaller the value of the elution amount and CEDI, the smaller the elution amount from the molded product (the better the elution resistance). The polylactic acid resin composition of the present invention and the molded product thereof can have a CEDI of less than 1 ppm, preferably less than 0.5 ppm. Thus, since CEDI is low, the amount of elution at the time of use is low, and it can be safely used as a food packaging container. In addition, since the amount of elution is small, deterioration of physical properties is also suppressed.

  Thus, the polylactic acid resin composition of the present invention and the resin molded body thereof are excellent in impact resistance, heat resistance, etc., and have high biodegradability. Therefore, the polylactic acid resin composition and the resin molded body thereof according to the present invention are used in various kinds of disposable containers (fresh food trays, instant food containers, fast food containers, lunch boxes, beverage bottles, mayonnaise and other seasoning containers). Food containers such as food containers, agricultural and horticultural containers such as nursery pots, blister pack containers, press-through pack containers, etc.), CD cases, cards such as clear files, credit cards, tableware such as spoons and straws, plastic models, It can be suitably used for various resin products such as resin sheets, resin films, and resin hoses, textile products such as clothing fibers, and non-woven fabrics. Furthermore, since the polylactic acid resin composition of the present invention has improved impact resistance, heat resistance, etc., compared to conventional polylactic acid resin compositions, it is more suitably used than conventional polylactic acid resin compositions. can do.

  Next, examples will be described together with comparative examples. However, the present invention is not limited to these examples as long as the gist thereof is not exceeded.

  First, prior to the examples and comparative examples, the following materials were prepared.

[Polylactic acid A-1]
Polylactic acid (trade name: 4032D, manufactured by Natureworks)

[Plasticizer B-1]
Polyoxyethylene sorbitan tristearate (oxyethylene group content: 48% by weight)

[Plasticizer B-2]
Polyoxyethylene sorbitan tribehenate (oxyethylene group content: 43% by weight)

[Plasticizer B-3]
Polyoxyethylene triisostearic acid hydrogenated castor oil (oxyethylene group content: 34% by weight, trade name: EMALEX RWIS-320, manufactured by Nippon Emulsion Co., Ltd.)

[Plasticizer B-4]
Polyoxyethylene glycerin triisostearate (oxyethylene group content: 50% by weight, trade name: EMALEX GWIS-320, manufactured by Nippon Emulsion Co., Ltd.)

[Plasticizer B-5]
Polyoxyethylene mannitan tristearate (oxyethylene group content: 48% by weight)

[Plasticizer B-6]
Polyoxyethylene sorbitan tristearate (oxyethylene group content: 31% by weight)

[Plasticizer B-7]
Polyoxyethylene sorbitan tristearate (oxyethylene group content: 65% by weight)

[Plasticizer B-8]
Polyoxyethylene glyceryl tristearate (oxyethylene group content: 20% by weight)

[Plasticizer B-9]
Polyoxyethylene sorbitan tri-12-hydroxystearate (oxyethylene group content: 45% by weight)

[Plasticizer b-1]
Ester compound of adipic acid and benzyl alcohol, diethylene glycol monomethyl ether (oxyethylene group content: 26% by weight, trade name: DAIFACTY-101, manufactured by Daihachi Chemical Industry Co., Ltd.)

[Plasticizer b-2]
Diester of succinic acid and triethylene glycol monomethyl ether (oxyethylene group content: 43% by weight)

[Plasticizer b-3]
Glycerol monostearate (oxyethylene group content: 0% by weight, trade name: Excel S-95, manufactured by Kao Corporation)

[Plasticizer b-4]
Polyoxyethylene glycerin tricaprylate (oxyethylene group content: 20% by weight)

[Plasticizer b-5]
Fatty acid ester of polyglycerin (oxyethylene group content: 0% by weight, trade name: Tyrabazole VR-05, manufactured by Taiyo Chemical Co., Ltd.)

[Crystal nucleating agent C-1]
N, N′-ethylenebis (12-hydroxystearic acid amide) (trade name: ITOHWAX J-530, manufactured by Ito Oil Co., Ltd.)

[Crystal nucleating agent C-2]
N, N′-ethylenebisstearic acid amide (trade name: ITOHWAX J-550S, manufactured by Ito Oil Co., Ltd.)

[Crystal nucleating agent C-3]
N, N′-xylylenebis (12-hydroxystearic acid amide) (trade name: ITOHWAX J-700, manufactured by Ito Oil Co., Ltd.)

[Crystal nucleating agent C-4]
N′-hydroxyethyl-12-hydroxystearylamide (trade name: ITOHWAX J-420, manufactured by Ito Oil Co., Ltd.)

[Crystal nucleating agent c-1]
Talc (trade name: MicroAce P-6, manufactured by Nihon Talc)

[Crystal nucleating agent c-2]
Montmorillonite in which interlayer ions are substituted with dioctadecyldimethylammonium ion (trade name: S-ben W, manufactured by Hojun Co.)

[Silica compound D-1]
Dry silica (trade name: Leolosil QS-102, manufactured by Tokuyama Corporation, silica content:> 99.9%)

[Silica compound D-2]
Silica modified with poly-D-lactic acid (obtained by Synthesis Example 1 below)
[Synthesis Example 1] 10.0 g of tetraethoxysilane was dissolved in 990 g of D-lactic acid (manufactured by Pulac Co., Ltd., 90% by mass aqueous solution), dehydrated and condensed at 130 ° C. for 4 hours while bubbling with nitrogen, and further 170 ° C. and 5 mmHg. After stirring for 12 hours under reduced pressure to perform dehydration polymerization, the fluid polymer obtained by the reaction was taken out and cooled and solidified to obtain silica modified with colorless and transparent poly-D-lactic acid (silica-containing 680 g of (amount: 0.42%) was obtained.

[Silica compound D-3]
Poly D-lactic acid silica dispersion (obtained by Synthesis Example 2 below)
[Synthesis Example 2] Silica modified with poly-D-lactic acid in the same manner except that 100 g of tetraethoxysilane of Synthesis Example 1 and 900 g of D-lactic acid (manufactured by Pulac Co., Ltd., 90% by mass) were changed to 900 g 630 g of (silica content: 4.6%) was obtained.

[Silica compound D-4]
Poly D-lactic acid silica dispersion (obtained by Synthesis Example 3 below)
[Synthesis Example 3] Silica modified with poly-D-lactic acid in the same manner except that 90 g of tetraethoxysilane and 10 g of 3-glycidoxypropyltriethoxysilane in Synthesis Example 1 were changed (silica content: 0.45%) was obtained.

[Silica compound D-5]
3-glycidoxypropyltriethoxysilane (trade name: KBE-403, manufactured by Shin-Etsu Silicone, silica content: 62.9%)

[Antioxidant E-1]
Hindered phenol antioxidant (trade name: IRGANOX 1076, manufactured by BASF)

[Examples 1 to 23, Comparative Examples 1 to 9]
Each of the above materials is blended in the proportions shown in Tables 1 to 4 below, and this is heated and kneaded using a twin screw extruder (manufactured by Technobel, KZW20-30MG) at a cylinder temperature of 160 to 190 ° C. As a result, pellets of the resin composition were obtained. The pellets were dried for 12 hours or more at a temperature of 70 ° C. under reduced pressure.

  Using the polylactic acid resin compositions (pellets) of Examples and Comparative Examples thus obtained, each characteristic was measured and evaluated according to the following criteria. The results are shown in Tables 1 to 4 below.

[Mold holding time]
A T-die extruder (manufactured by Technobel) was used to produce a 0.4 mm thick sheet from the pellets, and then the sheet was softened by heating from above and below with an infrared heater at about 300 ° C, followed by 90 ° C. The above-mentioned sheet was placed in a mold whose temperature was adjusted to a vacuum, and subjected to vacuum and pressure molding, followed by demolding to obtain a resin molded body. At the time of demolding, the shortest time (mold holding time) until the resin molded body can be taken out from the mold without deformation was measured. In addition, it shows that productivity is so high that this shortest time is short.

〔Heat-resistant〕
The resin molded body (molded body made of the polylactic acid resin composition) obtained by mold molding as described above was placed in an oven at 90 ° C. and held for 30 minutes. Then, a case where the molded body was not deformed at all after the heating was evaluated as ◯, and a case where the molded body was deformed was evaluated as x.

(Impact resistance)
Dropping ball impact test by placing a ball-shaped striker with a tip of 10 mm in diameter on the resin molded body obtained by molding as described above, and dropping a weight of 300 g or 500 g on the ball. Went. And the fall height (mm) of the weight when a crack generate | occur | produced in the resin molding was measured. In addition, even if the above drop altitude exceeds 1000 mm, the resin molded body was not cracked and expressed as “> 1000”, and when the above drop altitude was less than 50 mm, the resin molded body was cracked “<50”. ".

[CEDI]
The resin molded body (molded body made of a polylactic acid resin composition) obtained by mold molding as described above was measured for the amount of elution according to the elution test method stipulated by the FCN system of the US FDA, and the cumulative estimated daily intake (CEDI) was calculated. In the dissolution test, 10% ethanol was used as a pseudo solvent and heated at 66 ° C. for 2 hours. Then, the eluate eluted in the pseudo solvent was quantified by gas chromatography to obtain the elution amount, and CEDI (ppm) was calculated. In addition, it shows that it is excellent in elution resistance, so that this value is small.

  From the results of Tables 1 to 4, the polylactic acid resin compositions of the examples are both highly productive because the mold holding time is short compared to the polylactic acid resin compositions of the comparative examples. The resin molded body was not deformed by heating and was excellent in heat resistance. In addition, the polylactic acid resin compositions of the examples were all excellent in impact resistance as compared with the polylactic acid resin compositions of the comparative examples.

  The polylactic acid resin composition of the present invention and the resin molded product thereof are used in various disposable containers (fresh food trays, instant food containers, fast food containers, lunch boxes, beverage bottles, seasoning containers such as mayonnaise, etc.) Containers, seedling pots and other agricultural and horticultural containers, blister pack containers, press-through pack containers, etc.), CD cases, clear files, credit cards and other tableware, spoons, straws and other tableware, plastic models, resin sheets, It can be suitably used for various resin products such as resin films and resin hoses, textile products such as clothing fibers, and non-woven fabrics. Furthermore, since the polylactic acid resin composition of the present invention has improved impact resistance, heat resistance, etc. compared to the conventional polylactic acid resin composition, it is suitable for a wider field than the conventional polylactic acid resin composition. Can be used.

Claims (8)

A polylactic acid resin composition comprising the following components (B) to (D) together with the following component (A):
(A) Polylactic acid.
(B) A reaction product of at least one of a polyol and a polyol dehydration condensate, an alkylene oxide mainly composed of ethylene oxide, and a fatty acid having 12 to 24 carbon atoms.
(C) Fatty acid amide.
(D) Silica compound.   The polylactic acid resin composition according to claim 1, wherein the reaction product (B) contains 20 to 95% by weight of oxyethylene groups.   The polyol which is a material of the reaction product of the component (B) is at least one selected from the group consisting of glycerin, erythritol, pentaerythritol, xylitol, sorbitol, mannitol, galactitol and maltitol. Or the polylactic acid resin composition of 2.   The fatty acid amide as the component (C) is a bisamide compound obtained by reacting a fatty acid having 8 to 24 carbon atoms having a hydroxyl group with a compound having two amino groups. A polylactic acid resin composition as described in 1.   Content of the said (B) component is the range of 2-15 weight part with respect to 100 weight part of said (A) component, The polylactic acid resin composition as described in any one of Claims 1-4.   The polylactic acid resin according to any one of claims 1 to 5, wherein the content of the component (C) is in the range of 0.1 to 0.7 parts by weight with respect to 100 parts by weight of the component (A). Composition. Silica content of (SiO ₂₎ component, polylactic acid resin composition according to any one of claims 1 to 6 in the range of 0.01 to 2 parts by weight relative to component (A) 100 parts by weight object.   A resin molded body comprising the polylactic acid resin composition according to any one of claims 1 to 7.