Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/34—Silicon-containing compounds
  • C08K3/36—Silica
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
  • C08K5/0016—Plasticisers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers

Definitions

• the present invention relates to an aliphatic polyester resin composition having excellent flexibility and high heat resistance.
• Plastics are employed in various fields because of excellent chemical stability and high durability. However, plastics may cause problems upon disposal after use due to the stability. It is a social problem derived from landfill disposal and incineration of the wasted plastics. The plastics subjected to landfill disposal are not decomposed for a long period of time; thus, more landfills are necessary. Further, incineration of wasted plastics emits superheat to damage an incinerator. Furthermore, wasted plastics may generate a harmful substance.
• a biodegradable resin which is easily decomposed into water and carbon dioxide by microorganisms in earth or water.
• an aliphatic polyester resin is an excellent biodegradable resin, which is more environmentally friendly because it has a characteristic capable of being easily decomposed in the presence of water and therefore decomposed after disposal without causing environmental pollution when used as a general-purpose resin, and also which is more biologically friendly because it exerts no or little influence on the living body after achieving the purpose and then decomposed and absorbed in the living body when retained as a medical material in the living body.
• the aliphatic polyester resin caused problems when formed into a film, a filament or a molded article because of characteristics such as hardness, brittleness, and poor pliability at normal temperature. Also, the aliphatic polyester resin can not be used in hot water or a microwave oven and therefore used in limited purposes because an elastic modulus is rapidly lowered at a glass transition temperature or higher and the glass transition temperature is an upper temperature limit of the heat resistance.
• polylactic acid which is one of the aliphatic polyester resins
• polylactic acid is replaced by a copolymer with the other aliphatic polyester resin or a mixture of polylactic acid and the copolymer.
• EP 0 515 203 A discloses adding an aliphatic dihydric alcohol such as polyethylene glycol or polypropylene glycol to impart the flexibility to polylactic acid.
• JP Kokai No. 10-81815 discloses to impart the flexibility by adding silica, as an inorganic additive, and an aliphatic carboxylic acid amide to a mixture of an aliphatic polyester resin and a polyalkylene glycol. Since polylactic acid is hard at room temperature and has an elastic modulus of more than 10 ⁇ Pa, and the elastic modulus decreases quickly to less than 10 ⁇ Pa at a temperature of 100 °C or more, the heat resistance is poor.
• a desire of the present invention is to simultaneously impart the flexibility, heat resistance, and formability to an aliphatic polyester resin such as polylactic acid, to which the flexibility, the heat resistance and the formability are hardly imparted, simultaneously, according to the prior art.
• the present invention provides an aliphatic polyester resin composition
• an aliphatic polyester resin composition comprising an aliphatic polyester resin, a plasticizer, and hydrophilic silica particles, wherein the amount ofthe hydrophilic silica particles is within a range from 10 to 100 parts by weight based on 100 parts by weight of the total amount of the aliphatic polyester resin and the plasticizer.
• Fig. 1 is a graph showing the results of measuring an elastic modulus of resin films produced in the Examples and Comparative Examples of the present invention.
• Fig. 2 is a graph showing the results of measuring an elastic modulus of resin films produced in the Examples and Comparative Examples of the present invention.
• Fig. 3 is a graph showing the results of measuring an elastic modulus of resin films produced in the Examples and Comparative Examples of the present invention.
• Fig. 4 is a graph showing the results of measuring an elastic modulus of resin films produced in the Examples and Comparative Examples of the present invention.
• Fig. 5 is a graph showing the results of measuring an elastic modulus of resin films produced in the Examples and Comparative Examples of the present invention.
• a biodegradable resin having the flexibility and improved heat resistance by adding a plasticizer and a hydrophilic silica to an aliphatic polyester resin such as polylactic acid.
• Flexibility is imparted to the aliphatic polyester resin by adding a plasticizer such as aliphatic polyhydric alcohol, while the addition of hydrophilic silica particles forms a hydrogen bond with the plasticizer, and thus making it possible to improve the heat resistance of the aliphatic polyester resin. Further, by using the aliphatic polyester resin of the present invention, various shaped articles can be formed.
• a plasticizer such as aliphatic polyhydric alcohol
• hydrophilic silica particles forms a hydrogen bond with the plasticizer
• the aliphatic polyester resin composition ofthe present invention contains an aliphatic polyester resin, a plasticizer, and hydrophilic silica particles.
• the aliphatic polyester resin includes an aliphatic polyhydroxycarboxylic acid, an aliphatic polyester resin, and a mixture thereof described below.
• aliphatic polyhydroxycarboxylic acid for example, copolymer of a homopolymer such as polylactic acid or polyhydroxycaproic acid and lactic acid and the other aliphatic hydroxycarboxylic acid; (2) aliphatic polyester resin comprising a lactic acid unit, an aliphatic polyhydric carboxylic acid unit, and an aliphatic polyhydric alcohol unit; (3) aliphatic polyester resin containing a lactic acid unit and polyfunctional polysaccharides; (4) aliphatic polyester resin of an aliphatic polyhydric carboxylic acid such as polybutylene succinate and an aliphatic polyhydric alcohol; and (5) mixture of the above aliphatic polyhydroxycarboxylic acid and the above aliphatic polyester resin.
• aliphatic polyhydroxycarboxylic acid for example, copolymer of a homopolymer such as polylactic acid or polyhydroxycaproic acid and lactic acid and the other aliphatic hydroxycarboxylic acid
• the aliphatic polyhydroxycarboxylic acid and aliphatic polyester resin are copolymers, a random copolymer, an alternating copolymer, a block copolymer, and a graft copolymer are included.
• the concept of the mixture includes the concepts of a polymer blend and a polymer alloy.
• Examples of the aliphatic hydroxycarboxylic acid other than lactic acid, which constitutes the aliphatic polyhydroxycarboxylic acid, include glycolic acid, 3-hydroxybutyric acid, 4- hydroxybutyric acid, 4-hydroxyvaleric acid, 5-hydroxyvaleric acid, and 6-hydroxycaproic acid. These aliphatic hydroxycarboxylic acids are used alone as a homopolymer, or used in combination with lactic acid as a copolymer.
• the polylactic acid used in the present invention can be prepared by the method of directly subjecting L-lactic acid, D-lactic acid, or DL-lactic acid to dehydration polycondensation. Also it can be prepared by the method of subjecting lactide as a cyclic dimer of lactic acid to ring-opening polymerization. The ring-opening polymerization may be performed in the presence of a compound having a hydroxyl group, such as higher alcohol or hydroxycarboxylic acid.
• the copolymer of lactic acid and the other aliphatic hydroxycarboxylic acid can be prepared by the method of subjecting lactic acid and the hydroxycarboxylic acid to dehydration polycondensation.
• polylactic acid can be prepared by the method of subjecting lactide as a cyclic dimer of lactic acid and a cyclic compound of the aliphatic hydroxycarboxylic acid to ring-opening copolymerization.
• the polylactic acid may be prepared by any method.
• Examples ofthe aliphatic polyhydric carboxylic acid which is used in the preparation of the aliphatic polyester resin containing a lactic acid unit, an aliphatic polyhydric carboxylic acid unit and an aliphatic polyhydric alcohol unit or the aliphatic polyester resin of the aliphatic polyhydric carboxylic acid and the aliphatic polyhydric alcohol, include oxalic acid, succinic acid, malonic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, undecanoic diacid, dodecanoic diacid, and anhydrides thereof.
• These aliphatic polyhydric carboxylic acids may be acid anhydrides or mixtures with the acid anhydrides.
• Examples of the aliphatic polyhydric alcohol include ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, 1,3-butanediol, 1.4- butanediol, 3-methyl-l,5-pentanediol, 1,6-hexanediol, 1,9-nonanediol, neopentyl glycol, tetramethylene glycol and 1,4-cyclohexane dimethanol.
• the aliphatic polyester resin comprising a lactic acid unit, an aliphatic polyhydric carboxylic acid unit, and an aliphatic polyhydric alcohol unit can be prepared by the method of reacting the aliphatic polyhydric carboxylic acid and the aliphatic polyhydric alcohol with a copolymer of polylactic acid or lactic acid of the other hydroxycarboxylic acid, or the method of reacting the aliphatic polyhydric carboxylic acid and the aliphatic polyhydric alcohol with lactic acid.
• the aliphatic polyhydric carboxylic acid and the aliphatic polyhydric alcohol can be prepared by the method of reacting the aliphatic polyhydric carboxylic acid and the aliphatic polyhydric alcohol with lactide as the cyclic dimer of lactic acid or a cyclic ester of the hydroxycarboxylic acid.
• the aliphatic polyester resin can be prepared by any method.
• the aliphatic polyester resin of the aliphatic polyhydric carboxylic acid and the aliphatic polyhydric alcohol can be prepared by the method of reacting the aliphatic polyhydric carboxylic acid with the aliphatic polyhydric alcohol.
• polyfunctional polysaccharides used in the preparation of the aliphatic polyester resin containing a lactic acid unit and polyfunctional polysaccharides include cellulose, cellulose nitrate, cellulose acetate, methylcellulose, ethylcellulose, carboxymethylcellulose, nitrocellulose, cellophane, viscose rayon, regenerated cellulose such as cupra, hemicellulose, starch, amylopectin, dextrin, dextran, glycogen, pectin, chitin, chitosan, and mixtures and derivatives thereof.
• the aliphatic polyester resin containing a lactic acid unit and polyfunctional polysaccharides can be prepared by the method of reacting the polyfunctional polysaccharides and lactic acid or polylactic acid with a copolymer of lactic acid and hydroxycarboxylic acid. Also it can be prepared by the method of reacting the polyfunctional polysaccharides with lactide as the cyclic dimer of lactic acid or cyclic esters of the hydroxycarboxylic acid.
• the aliphatic polyester resin may be prepared by any method.
• various aliphatic polyester resins described above can be used.
• those containing a lactic acid component for example, a copolymer of a homopolymer such as polylactic acid, polybutylene succinate or polyhydroxycaproic acid, lactic acid and an aliphatic hydroxycarboxylic acid other than lactic acid (in case the transparency is required, those containing lactic acid in a weight ratio of 50% or more are preferred) and an aliphatic polyester resin of lactic acid, an aliphatic polyhydric carboxylic acid and an aliphatic polyhydric alcohol (in case the transparency is required, those containing lactic acid in a weight ratio of 50% or more are preferred) are preferably used.
• the molecular weight of the aliphatic polyester resin used in the present invention is not specifically limited as far as the resulting molded article such as container, film, sheet, or plate exhibits substantially sufficient mechanical and physical properties.
• the weight-average molecular weight of the aliphatic polyester resin used in the present invention is within a range from 10,000 to 5,000,000, preferably from 30,000 to 3,000,000, more preferably from 50,000 to 2,000,000, still more preferably from 70,000 to 1,000,000, and most preferably from 90,000 to 500,000.
• plasticizer refers to any compound having the effect capable of lowering the elastic modulus of the resin by adding to the resin, and the compound may be in the form of gas, liquid, or solid and may be an organic or inorganic compound.
• the plasticizer used in the aliphatic polyester resin composition may be at least one selected from phthalic acid derivative, adipic acid derivative, azelaic acid derivative, sebacic acid derivative, maleic acid derivative, fumaric acid derivative, trimellitic acid derivative, citric acid derivative, fatty acid derivative, sulfonic acid derivative, phosphoric acid derivative, glycol derivative, glycerin derivative, paraffin derivative, diphenyl derivative, epoxy derivative and polymer such as polyester, polyether or polyglycerin, which are substituted or added with hydroxyl group, ether group, ester group, carboxyl group, acyl group, amino group, nitro group, sulfo group, or halogen.
• phthalic acid derivative examples include dimethyl phthalate, diethyl phthalate, dibutyl phthalate, diisobutyl phthalate, diamyl phthalate, dihexyl phthalate, butyloctyl phthalate, butylisodecyl phthalate, butyllauryl phthalate, di- (2-ethylhexyl) phthalate, di-n-octyl phthalate, di-2-octyl phthalate, butyl coconut alkyl phthalate, phthalate of higher alcohol by high-pressure reduction of coconut oil, phthalate of higher alcohol, mixed alcohol phthalate, straight-chain alcohol phthalate, dilauryl phthalate, diheptyl phthalate, diisooctyl phthalate, octyldecyl phthalate, n-octyl,n-decyl phthalate, diisodecyl
• Examples of usable adipic acid derivative include di-n-butyl adipate, diisobutyl adipate, di-(2-ethylhexyl) adipate, diisooctyl adipate, diisodecyl adipate, octyldecyl adipate, dicapryl adipate, benzyl-n-butyl adipate, polypropylene adipate, polybutylene adipate, dibutoxyethyl adipate and benzyloctyl adipate; and examples of usable azelaic acid derivative include di-2(-ethylhexyl) azelate, diisooctyl azelate, di-2-ethylhexyl-4- thioazelate, di-n-hexylazelate and diisobutyl azelate; and specific examples of the sebacic acid derivative,
• maleic acid derivative examples include di-n-butyl maleate, dimethyl maleate, diethyl maleate, di-(2-ethylhexyl) maleatea, and dinonyl maleate; and examples of the fumaric acid derivative, which can be used, include dibutyl fumarate and di-(2-ethylhexyl) fumarate.
• fumaric acid derivative examples include dibutyl fumarate and di-(2-ethylhexyl) fumarate.
• trimellitic acid derivative examples include tri-(2- ethylhexyl) trimellitate, triisodecyl trimellitate, n-octyl, n-decyl trimellitate, triisooctyl trimellitate, and diisooctylmonoisodecyl trimellitate.
• citric acid derivative examples include triethyl citrate, tri-n-butyl citrate, acetyl triethyl citrate, acetyl tri-n-butyl citrate, acetyl tri-n-octyl, n-decyl citrate, and acetyl tri-(2-ethylhexyl) citrate.
• fatty acid derivative examples include methyl oleate, butyl oleate, methoxyethyl oleate, tetrahydrfurfuryl oleate, glyceryl monooleate, diethylene glycol monooleate, methylacetyl ricinoleate, butylacetyl ricinoleate, glyceryl monoricinoleate, diethylene glycol monoricinoleate, glyceryl tri-(acetyl ricinoleate), alkylacetyl ricinoleate, n-butyl stearate, glyceryl mono stearate, diethylene glycoldi stearate, stabilized pentachloromethyl stearate, chlorinated methyl stearate, chlorinated alkyl stearate, diethylene glycol monolaurate, diethylene glycol dipelargonate, triethylene glycol dipelargonate, butylcellosolv
• Examples of the sulfonic acid derivative, which can be used, include benzenesulfonebutylamide, o-toluenesulfonamide, p-toluenesulfonamide, N-ethyl-p- toluenesulfonamide, o-tolueneethylsulfonamide, p-tolueneethylsulfonamide, N- cyclohexyl-p-toluenesulfonamide, alkyl sulfonate ester of phenol and cresol, and sulfonamide-formamide.
• Examples of the phosphoric acid derivative which can be used, include triethyl phosphate, tributyl phosphate, tri-(2-ethylhexyl) phosphate, triphenyl phosphate, cresyldiphenyl phosphate, tricresyl phosphate, tritolyl phosphate, trixylyl phosphate, phosphate containing at most 1% of an ortho-cresol isomer, alkylallyl phosphate, tris(chloroethyl) phosphate, diphenylmono-o-xenyl phosphate, and diphenylxylenyl phosphate.
• glycol derivative examples include triethylene glycol di- (2-ethylbutylate), triethylene glycol di-(2-ethylhexoate), polyethylene glycol di(2- ethylhexoate), dibutylmethylenebis-thioglycolate, polyethylene glycol, and polyglycol ether; and examples of the glycerin derivative, which can be used, include glycerol monoacetate, glycerol diacetate, glycerol triacetate, glycerol tributylate, glycerol O 2004/055104
• tripropionate tripropionate
• glycerol ether acetate tripropionate
• paraffin derivative or diphenyl derivative examples include chlorinated paraffin, chlorinated diphenyl, chlorinated triphenyl, chlorinated polyphenyl and partially hydrogenated triphenyl; and examples of the epoxy derivative, which can be used, include butylepoxy stearate, epoxy monoester, octylepoxy stearate, epoxidated butyloleate, epoxy fatty acid ester, di-(2-ethylhexyl)4,5-epoxycyclohexane-l,2- carboxylae, epoxidated semidrying oil, epoxidated fatty acid monoester, epoxidated triglyceride, epoxybutyl stearate, epoxy octyl stearate, epoxydecyl stearate, epoxidated soybean oil, methylepoxy hydrostearate, glyceryltri-(epoxyacetoxystearate), isooc
• Examples of the polymer, polyester, polyether, polyglycerin, etc., which can be used, include sebacic acid polyester, adipic acid polyester, phthalic acid polyester, acetylated polyester, alkyd resin, low-molecular weight polystyrene, poly- -methylstyrene, unsaturated fatty acid nitrile, dibutoxyehoxyethyl formal, isobutylate, ether thioether, dibenzyl ether, phenol derivative, and dimethyl polysiloxane.
• the amount of the plasticizer can vary according to the kind of the aliphatic polyester resin and the kind of the plasticizer. The amount may be controlled so that the aliphatic polyester resin composition plasticized by the plasticizer is softened at the temperature lower than a melting point of the aliphatic polyester resin and can be molded, and is usually within a range from 2.0 to 50 parts by weight based on 100 parts by weight of the aliphatic polyester resin.
• the hydrophilic silica particles to be added in the aliphatic polyester resin composition of the present invention can form a hydrogen bond with the plasticizer and means both hydrophilic silica particles and particles coated with the hydrophilic silica.
• the hydrophilic silica is silica having a SiOH (silanol group) formed by bonding silicon with a hydroxyl group.
• the hydrophilic silica is desirably amorphous and may be prepared by either a thermal decomposition method or a precipitation method.
• the silica prepared by the thermal decomposition method can be obtained by continuously decomposing silicon tetrachloride (SiCl 4 ) with intense heating at 1000 °C in the presence of hydrogen and oxygen.
• the silica prepared by the precipitation method is obtained by reacting a O 2004/055104
• an alkali metal silicate for example, sodium silicate with an acid.
• an alkali metal silicate for example, sodium silicate with an acid.
• FINE SEAL B trade name, manufactured by Tokuyama Soda Co., Ltd.
• AEROSIL 200 trade name, manufactured by Japan Aerosil Ltd.
• the particles coated with the hydrophilic silica also include particles coated entirely or partially with silica, particularly mineral particles coated entirely or partially with silica, and examples thereof include titanium oxide-containing silica beads which are commercially available from Toray Industries, Inc. under the trade name of Torayceram S- ITTM; titanium oxide-containing silica alumina microsphere which is commercially available from Zeelan Co. under the trade name of Z-Light-Sphere W1O12TM; silica/titanium oxide particles (particle diameter: 106 to 500 ⁇ m) synthesized by an amorphous precipitation method, which are commercially available from Crossfield Co.
• the average particle diameter of the hydrophilic silica particle is not specifically limited, but is within a range from 5 nm to 30 nm. Especially, in case optically transparency is required, it is within a range from 5 nm to 100 nm. When the average particle diameter of the hydrophilic silica particle is larger than 100 nm, light is scattered and transparency decreases.
• the amount of the hydrophilic silica particle is controlled within a range from 10 to 100 parts by weight, or 15 to 40 parts by weight based on 100 parts by weight ofthe total amount of the aliphatic polyester resin and the plasticizer.
• the amount of the hydrophilic silica particle is less than 10 parts by weight, heat resistance is insufficient.
• the amount is more than 100 parts by weight, resin strength decreases and formability decreases.
• antioxidants antioxidants, ultraviolet absorbers, antistatic agents, lubricants, coloring pigments, and a small amount of other resins can be added for the purposes of improving physical properties such as elastic modulus, tensile strength, flexural strength, mechanical strength, heat resistance, and weatherability.
• various elastomers for example, SBR (styrene-butadiene rubber), NBR (acrylonitrile-butadiene rubber), SBS (polystyrene- polybutadiene-polystyrene) type thermoplastic elastomers), additives (for example, nucleating agents, pigments, stabilizers, releasants, flame retardants, antioxidants, ultraviolet absorbers, antibacterial agent, and dyes), fillers (for example, calcium carbonate, clay, carbon black, impact-resistant core/shell type particles), pigments (for example, titanium oxide, metallic pigments and pearlescent pigments) can be appropriately used according to the purposes and applications.
• the aliphatic polyester resin, the plasticizer, the hydrophilic silica, and other additives can be mixed in the form of a solid using publicly known kneading means such as Henschel mixer and ribbon blender.
• molded articles can be produced by an injection molding method, an extrusion blow molding method, an extrusion stretching blow molding method, an injection blow molding method, an injection stretching blow molding method, a thermoforming method, or a compression molding method.
• film-, sheet- and plate-shaped molded articles can be produced by an inflation molding method or a T-die molding method.
• the aliphatic polyester resin composition of the present invention has the flexibility at normal temperature and it is not necessary to stretch to increase the crystallinity when used as a thin film or fibers. Since a stretching operation is not required, it is possible to impart sufficient durability to a thick sheet such as doormat.
• a molded article having proper elastic modulus even at high temperature of 100 °C or higher can be produced. Therefore, it became possible to apply an aliphatic polyester resin, particularly polylactic acid, which had hitherto been used only in stationery and packaging materials, to various uses such as film-shaped molded articles having different thickness and shape in outdoor, automotive, and electrical fields. Specifically, mechanical fasteners, floor mats composed of thick fibers, agricultural films, various containers for beverages and cosmetics, and packaging films for foods can be formed by the above method.
• a composition was prepared and the elastic modulus were measured according to Example 1, except that the amount ofthe hydrophilic amorphous silica particles is changed to 40 parts by weight. Comparative Example 1
• Polylactic acid alone used in Example 1 was formed into a film at 150 °C and the elastic modulus were measured.
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 1, except that polyethylene glycol was not added.
• Comparative Example 3 A composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 1, except that the hydrophilic amorphous silica particles were not added.
• Fig. 1 As shown in Fig. 1, when using polylactic acid alone (Comparative Example 1), the resulting product is hard having an elastic modulus of 10 ⁇ Pa at 50 °C or lower.
• the elastic modulus When polyethylene glycol is added to polylactic acid (Comparative Example 3), the elastic modulus is 1.0 x 10 ⁇ Pa or less at room temperature (25 °C) and the flexibility is imparted, while the temperature dependence of the elastic modulus is high and the elastic modulus at 40 °C is lower than that of polylactic acid. Therefore, the heat resistance is poor.
• Example 1 the addition of 20 parts by weight of hydrophilic amorphous silica particles to 100 parts by weight of the total amount of the polylactic acid and the plasticizer makes it possible to prevent lowering of the elastic modulus at high temperature, and thus the same elastic modulus as the original elastic modulus of polylactic acid can be maintained even at 80 °C or higher.
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 1, except that polyethylene glycol having a weight- average molecular weight of 200 was changed to polyethylene glycol having a number- average molecular weight of 1000.
• Example 4
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 1, except that the amount ofthe polyethylene glycol was changed to 15 parts by weight.
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 3, except that the hydrophilic amorphous silica particles were not added.
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 3, except that the amount of the hydrophilic amorphous silica particles was changed to 10 parts by weight.
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 4, except that the amount of the hydrophilic amorphous silica particles was changed to 10 parts by weight.
• polylactic acid LACTY9800, manufactured by Shimadzu Corp.
• polyethylene glycol having a weight-average molecular weight of 2,000 was added and the mixture was kneaded at 150 °C and 30 rpm using a Brabender mixer.
• AEROSIL 200 having an average primary particle diameter of 12 nm, manufactured by Japan Aerosil Ltd.
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 5, except that the hydrophilic amorphous silica particles were not added.
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 5, except that hydrophobic amorphous silica particles ("AEROSIL RX200" having an average primary particle diameter of 12 nm, manufactured by Japan Aerosil Ltd.) were added instead of the hydrophilic amorphous silica particles.
• hydrophobic amorphous silica particles (“AEROSIL RX200” having an average primary particle diameter of 12 nm, manufactured by Japan Aerosil Ltd.) were added instead of the hydrophilic amorphous silica particles.
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 1, except the polyethylene glycol having a weight- average molecular weight of 200 was changed to a polyethylene glycol having a number- average molecular weight of 1000.
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 1, except the polyethylene glycol having a weight- average molecular weight of 200 was changed to diglycerol ester having an acetylation ratio of 50% or more (manufactured by Riken Vitamin Co., Ltd., "LIKEMAL PL-710"). Comparative Example 9
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 6, except that the hydrophilic amorphous silica particles were not added.
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 7, except that the hydrophilic amorphous silica particles were not added.
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 3, except the polylactic acid having a weight- average molecular weight of 120,000 was changed to polyethylene succinate having a weight-average molecular weight of 240,000 (manufactured by Nihon Syokubai Co., Ltd., Runare SE-P1000).
• Example 8 The polyethylene succinate having a weight-average molecular weight of 240,000 alone used in Example 8 was formed into film and the elastic modulus were measured according to Example 1. Comparative Example 12
• a composition was prepared, it was formed into a film, and the elastic modulus were measured according to Example 8, except that the hydrophilic amorphous silica particles were not added.
• the flexibility was evaluated by the elastic modulus, and the symbol O means that the elastic modulus is 1 x 10 ⁇ or less at 20 °C; ⁇ means that the elastic modulus is 1 x 10 ⁇ or less at 20 to 30 °C; andX means that the elastic modulus is 1 x 10 ⁇ or more at 40 °C.
• the heat resistance is also evaluated by the elastic modulus, and the symbol O means that the elastic modulus is 1 x 10 ⁇ or more at 100 °C; ⁇ means that the elastic modulus is 1 x 10 ⁇ or less at 90 to 100 °C; and X means that the elastic modulus is 1 x 10° " or less at 90 °C.

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