JP2000007812A - Composition for producing foam, production of foam and foam - Google Patents

Abstract

PROBLEM TO BE SOLVED: To prepare a composition for producing foam capable of exhibiting excellent foaming property and moldability, land suitable for foaming by adding a thickener and a decomposition-type blowing agent to a biodegradable polyactic acid-based resin in a specific ratio. SOLUTION: This composition contains (A) 100 pts.wt. polylactic acid-based resin, (B) 0.01-20 pts.wt. thickener (e.g. a multivalent isocyanate, a polybasic acid anhydride, or the like) and (C) 0.1-20 pts.wt. decomposition-type blowing agent (e.g. an inorganic blowing agent such as sodium bicarbonate, an organic blowing agent such as azodicarbonamide). The composition is melt-foamed, and a polylactic acid-based foam or sheet both improved in foaming moldability is obtained. Melt tension in melt-foaming is sufficient and it is possible to produce molded foam in a high expansion ratio.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

TECHNICAL FIELD The present invention relates to a composition for producing a polylactic acid-based foamable resin foam. Furthermore, the present invention relates to a method for obtaining a foam, a foam as a molded product, and a sheet.

[0002]

2. Description of the Related Art Generally, foam materials are manufactured from resins such as polyethylene, polypropylene, and polystyrene.
It is used in other fields by utilizing its performances such as light weight, heat insulation, soundproofing, and cushioning. However, these foamed materials are difficult to recover and reuse after use,
Since it is hardly decomposed in the natural environment, it remains in the ground semi-permanently. In addition, abandoned plastics have caused problems such as spoiling the landscape and destroying the living environment of marine life.

On the other hand, lactic acid-based polymers such as polylactic acid and copolymers of lactic acid and other aliphatic hydroxycarboxylic acids, and aliphatic polyhydric alcohols and aliphatic polyhydric alcohols include thermoplastic resins having biodegradability. Aliphatic polyesters derived from carboxylic acids have been developed. Some of these polymers are 100% biodegradable within months to one year in animals or, when placed in soil or seawater, begin to degrade within weeks in a humid environment, with about 1 It disappears in a few years from the year. Furthermore, the decomposition products have the property of becoming lactic acid, carbon dioxide, and water that are harmless to the human body.

[0004] In particular, polylactic acid has recently been produced in large quantities and inexpensively by fermentation of L-lactic acid as a raw material, has a high decomposition rate in compost, has resistance to mold, and has a high resistance to food. Due to its excellent characteristics such as odor resistance and coloring resistance, it is expected that its field of use will be expanded.

[0005] However, polylactic acid generally has a low melt tension, so that it is still insufficient for molding methods such as foam molding. That is, since there is no sufficient melt tension at the time of melt molding, it is difficult to obtain a foam molding having a high magnification, and it is difficult to find appropriate foam molding conditions.

JP-A-4-304244, JP-A-5-304244
JP-A-140361, JP-A-6-287347, etc., describe a molding technique relating to foaming of a polylactic acid-based resin composition, but effectively perform foam molding of an aliphatic polyester such as polylactic acid. The method is still inadequate.

[0007]

The problem to be solved by the present invention is to provide a polylactic acid-based resin composition having excellent foamability and moldability during foam molding, a method for producing a foam,
An object of the present invention is to provide a sheet made of a foam.

[0008]

Means for Solving the Problems As a result of intensive studies on polylactic acid-based resins, the present inventors have found that by adding a specific foaming nucleating agent and a foaming auxiliary to a polylactic acid-based resin at a specific ratio, the above-mentioned properties can be obtained. The present inventors have found a foamable resin composition that satisfies the above-mentioned problems, and a method for producing a foam, and have completed the present invention.
That is, the present invention is specified by the following items [1] to [8].

[1] (A) 100 parts by weight of a polylactic acid-based resin based on 100 parts by weight of a polylactic acid-based resin;
(B) 0.01 to 20 parts by weight of a thickening agent and (C) 0.1 to 20 parts by weight of a decomposable foaming agent, for producing a polylactic acid-based resin foam. Composition.

[2] (A) 100 parts by weight of polylactic acid-based resin, based on 100 parts by weight of polylactic acid-based resin,
And (B) a resin composition containing 0.01 to 20 parts by weight of a thickener, and (C) a decomposable foaming agent of 0.1 to 2 parts.
A composition for producing a polylactic acid-based resin foam, comprising 0 parts by weight.

[3] (A) 100 parts by weight of polylactic acid-based resin, based on 100 parts by weight of polylactic acid-based resin,
A composition comprising (B) 0.01 to 20 parts by weight of a thickener and (C) 0.1 to 20 parts by weight of a decomposable foaming agent,
A method for producing a polylactic acid-based resin foam, characterized by performing melt foam molding.

[4] (A) 100 parts by weight of polylactic acid-based resin, based on 100 parts by weight of polylactic acid-based resin,
And (B) a resin composition containing 0.01 to 20 parts by weight of a thickener, and (C) a decomposable foaming agent of 0.1 to 2 parts.
A method for producing a polylactic acid-based resin foam, comprising subjecting a composition containing 0 parts by weight to melt foam molding.

[5] (A) 100 parts by weight of polylactic acid-based resin, based on 100 parts by weight of polylactic acid-based resin,
And (B) adding 0.1 to 20 parts by weight of a decomposable foaming agent at the time of melt-molding a resin composition containing 0.01 to 20 parts by weight of a thickener; A method for producing a polylactic acid-based resin foam.

[6] A method for producing a polylactic acid-based foam, comprising subjecting the composition according to [1] or [2] to melt foam molding.

[7] A polylactic acid-based foam obtained by the production method according to any one of [3] to [6].

[8] A polylactic acid-based foam sheet obtained by the production method according to any one of [3] to [6].

[0017]

BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail.

[Types of thickeners] The thickeners used in the present invention include (1) polyvalent isocyanate compounds, (2) polybasic anhydrides, (3) cyclic imino esters, (4) A) cyclic imino ethers, (5) aromatic hydroxycarboxylic acids, (6) polyamine compounds, (7) polyhydric alcohols, (8) epoxy compounds, (9) polyfunctional aziridine compounds, (10) lactams , (11) lactones, (1
2) diethylene glycol bischloroformate,
(13) alkaline earth metal compound, (14) alkali metal salt, (15) water-soluble polymer, (16) cellulose derivative, (17) natural rubber, (18) thermoplastic resin and the like. These may be used alone or in combination of two or more as long as the purpose is not impaired.

The polyvalent isocyanate used in the present invention is, for example, hexamethylene diisocyanate, 2,4
-Tolylene diisocyanate, a mixture of 2,4-tolylene diisocyanate and 2,6-tolylene diisocyanate, 4,4'-diphenylmethane diisocyanate,
Xylene diisocyanate, isophorone diisocyanate, trimethylene diisocyanate, tetramethylene diisocyanate, pentamethylene diisocyanate,
1,2-propylene diisocyanate, 2,3-butylene diisocyanate, 1,3-butylene diisocyanate, 2,4,4-trimethylhexamethylene diisocyanate, dodecamethylene diisocyanate, 2,6- Diisocyanate methyl caproate, 1,3-cyclopentane diisocyanate, 1,4-cyclohexane diisocyanate, 1,3-cyclohexane diisocyanate, 4,4′-methylenebis (cyclohexyl isocyanate), methyl- 2,4-cyclohexane diisocyanate, methyl-2,6-cyclohexane diisocyanate, 1,4-bis (isocyanatomethyl) cyclohexane, 1,3-bis (isocyanatomethyl) cyclohexane, dicyclohexyl-4,4- Methane-diisocyanate, phenyl Range isocyanate, 4,4'-
Diphenyl diisocyanate, 1,5-naphthalenediisocyanate, 3,3,5-trimethyl-1-isocyanato-3-isocyanatomethylcyclohexane, di (2-isocyanatoethyl) bicyclo [2,2,1]
Hept-5-ene-2,3-dicarboxylate, 4,
4′-toluidine diisocyanate, dianisidine diisocyanate, 4,4′-diphenyl ether diisocyanate, ω, ω′-diisocyanate-1,4-diethylbenzene, 1,3-tetramethylxylylene diisocyanate, 1,4-tetramethylxylylene diisocyanate, hydrogenated diphenylmethane diisocyanate,
Examples thereof include hydrogenated tolylene diisocyanate and hydrogenated xylylene diisocyanate. Among these, trimers such as buret type, adduct type and nullate type can be used.

The polybasic anhydrides used in the present invention include, for example, maleic anhydride, succinic anhydride, itaconic anhydride,
Glutaric anhydride, adipic anhydride, phthalic anhydride, citraconic anhydride, trimellitic anhydride, pyromellitic anhydride, 2,3-benzophenone dicarboxylic anhydride, 3,
4-benzophenone dicarboxylic anhydride, 2,3-dicarboxyphenyl-phenyl-ether anhydride, 3,4
-Dicarboxyphenyl-phenyl-ether anhydride,
3,4-biphenyldicarboxylic anhydride, 2,3-dicarboxyphenyl-phenyl-sulfonic anhydride, 2,
3-dicarboxyphenyl-phenyl-sulfide,
1,2-naphthalenedicarboxylic anhydride, 2,3-naphthalenedicarboxylic anhydride, 1,8-naphthalenedicarboxylic anhydride, 2,3-anthracenedicarboxylic anhydride, 1,9-anthracenedicarboxylic anhydride, Ethylene tetracarboxylic dianhydride, cyclopentane tetracarboxylic dianhydride, 3,3 ', 4,4'-benzophenone tetracarboxylic dianhydride, 2,2', 3,3'-benzophenone tetracarboxylic dianhydride Anhydride, 3,3 ',
4,4'-biphenyltetracarboxylic dianhydride, 2,
2 ', 3,3'-biphenyltetracarboxylic dianhydride, 2,2'-bis (3,4-dicarboxyphenyl)
Propane dianhydride, bis (3,4-dicarboxyphenyl) ether dianhydride, bis (3,4-dicarboxyphenyl) sulfonic dianhydride, 1,1-bis (2,3-
Dicarboxyphenyl) ethane dianhydride, bis (2,3
-Dicarboxyphenyl) methane dianhydride, 1,1-bis (2,3-dicarboxyphenyl) ethane dianhydride,
Bis (3,4-dicarboxyphenyl) methane dianhydride, 2,3,6,7-naphthalenetetracarboxylic dianhydride, 1,4,5,8-naphthalenetetracarboxylic dianhydride, 1,2,2 5,6-naphthalenetetracarboxylic dianhydride, 1,2,3,4-benzenetetracarboxylic dianhydride, 3,4,9,10-berylenetetracarboxylic dianhydride, 2,3,6 , 7-anthracenecarboxylic dianhydride, 1,2,7,8-phenanthrenecarboxylic dianhydride and the like.

Examples of the cyclic imino esters used in the present invention include an oxazolone compound having a 5-membered imino ester ring, an oxazinone compound or a benzoxazinone compound having a 6-membered imino ester ring.

As the oxazolone compound, for example, 2
-Oxazolin-5-one, 3-oxazolin-5-one, 2-oxazolin-4-one, 3-oxazoline-
2-one, 4-oxazolin-2-one, 4-methyl-
2-oxazolin-5-one, 2-methyl-3-oxazolin-5-one, 5-methyl-2-oxazoline-4
-One, 5-methyl-3-oxazolin-2-one,
2,2′-bis (5 (4H) -oxazolone), 2,2
'-Methylenebis (5 (4H) -oxazolone), 2,
2'-ethylenebis (5 (4H) -oxazolone),
2,2'-tetramethylenebis (5 (4H) -oxazolone), 2,2'-hexamethylenebis (5 (4H)-
Oxazolone), 2,2'-decamethylenebis (5 (4
H) -oxazolone), 2,2′-p-phenylenebis (5 (4H) -oxazolone), 2,2′-m-phenylenebis (5 (4H) -oxazolone), 2,2′-naphthalenebis ( 5 (4H) -oxazolone), 2,2 ′
-Diphenylenebis (5 (4H) -oxazolone),
2,2 '-(1,4-cyclohexylene) bis (5 (4
H) -oxazolone), 2,2'-bis (4-methyl-
5 (4H) -oxazolone), 2,2′-methylenebis (4-methyl-5 (4H) -oxazolone), 2,2 ′
-Ethylenebis (4-methyl-5 (4H) -oxazolone), 2,2'-tetramethylenebis (4-methyl-5
(4H) -oxazolone), 2,2′-hexamethylenebis (4-methyl-5 (4H) -oxazolone), 2,
2'-decamethylenebis (4-methyl-5 (4H) -oxazolone), 2,2'-p-phenylenebis (4-methyl-5 (4H) -oxazolone), 2,2'-m-phenylenebis (4-methyl-5 (4H) -oxazolone), 2,2′-naphthalenebis (4-methyl-5 (4
H) -oxazolone), 2,2′-diphenylenebis (4-methyl-5 (4H) -oxazolone), 2,2 ′
-(1,4-cyclohexylene) bis (4-methyl-5
(4H) -oxazolone), 2,2′-bis (4,4-
Dimethyl-5 (4H) -oxazolone), 2,2'-methylenebis (4,4-dimethyl-5 (4H) -oxazolone), 2,2'-ethylenebis (4,4-dimethyl-
5 (4H) -oxazolone), 2,2′-tetramethylenebis (4,4-dimethyl-5 (4H) -oxazolone), 2,2′-hexamethylenebis (4,4-dimethyl-5 (4H) -Oxazolone), 2,2'-octamethylenebis (4,4-dimethyl-5 (4H) -oxazolone), 2,2'-decamethylenebis (4,4-dimethyl-5 (4H) -oxazolone), 2,2′-p-phenylenebis (4,4-dimethyl-5 (4H) -oxazolone), 2,2′-m-phenylenebis (4,4-dimethyl-5 (4H) -oxazolone), 2, 2′-naphthalenebis (4,4-dimethyl-5 (4H) -oxazolone), 2,2′-diphenylenebis (4,4-dimethyl-5 (4H) -oxazolone), 2,2 ′-(1 , 4-
Cyclohexylene) -bis (4,4-dimethyl-5 (4
H) -oxazolone), 2,2′-bis (4-isopropyl-5 (4H) -oxazolone), 2,2′-methylenebis (4-isopropyl-5 (4H) -oxazolone), 2,2′-ethylene Bis (4-isopropyl-5
(4H) -oxazolone), 2,2′-tetramethylenebis (4-isopropyl-5 (4H) -oxazolone), 2,2′-hexamethylenebis (4-isopropyl-5 (4H) -oxazolone), 2 , 2'-p-phenylenebis (4-isopropyl-5 (4H) -oxazolone), 2,2'-m-phenylenebis (4-isopropyl-5 (4H) -oxazolone), 2,2'-naphthalenebis (4-isopropyl-5 (4H) -oxazolone), 2,2'-bis (4-isobutyl-5 (4H)-
Oxazolone), 2,2'-methylenebis (4-isobutyl-5 (4H) -oxazolone), 2,2'-ethylenebis (4-isobutyl-5 (4H) -oxazolone), 2,2'-tetramethylenebis (4-isobutyl-5 (4H) -oxazolone), 2,2′-hexamethylenebis (4-isobutyl-5 (4H) -oxazolone), 2,2′-p-phenylenebis (4-isobutyl-5 ( 4H) -oxazolone), 2,2′-m-phenylenebis (4-isobutyl-5 (4H) -oxazolone), 2,2′-m-naphthalenebis (4-isobutyl-5 (4H) -oxazolone) and the like And especially 2
-Oxazolin-5-one, 2,2'-bis (5 (4
H) -Oxazolone) is preferred.

As the oxazinone compound, for example,
2,2'-bis (3,1-benzoxazin-4-one), 2,2'-methylenebis (3,1-benzoxazin-4-one), 2,2'-ethylenebis (3,1-
Benzoxazin-4-one), 2,2′-tetramethylenebis (3,1-benzoxazin-4-one),
2,2'-hexamethylenebis (3,1-benzoxazin-4-one), 2,2'-decamethylenebis (3
1-benzoxazin-4-one), 2,2'-p-phenylenebis (3,1-benzoxazin-4-one), 2,2'-m-phenylenebis (3,1-benzoxazine-4) -One), 2,2'-naphthalenebis (3,1-benzoxazin-4-one), 2,2'-
(4,4′-diphenylene) bis (3,1-benzoxazin-4-one), 2,2′-bis (4,5-dihydro-1,3,6H-oxazin-6-one), 2,2 ´-
Methylene bis (4,5-dihydro-1,3,6H-oxazin-6-one), 2,2′-ethylenebis (4,5-
Dihydro-1,3,6H-oxazin-6-one), 2,
2'-tetramethylenebis (4,5-dihydro-1,
3,6H-oxazin-6-one), 2,2'-p-phenylenebis (4,5-dihydro-1,3,6H-oxazin-6-one), 2,2'-m-phenylenebis (4,
5-dihydro-1,3,6H-oxazin-6-one),
2,2'-bis (4-methyl-5-hydro-1,3,6
H-oxazin-6-one), 2,2'-bis (4-methyl-5-hydro-1,3,6H-oxazin-6-one), 2,2'-ethylenebis (4-methyl-5) -Hydro-1,3,6H-oxazin-6-one), 2,2 '
-P-phenylenebis (4-methyl-5-hydro-1,
3,6H-oxazin-6-one), 2,2'-m-phenylenebis (4-methyl-5-hydro-1,3,6H
-Oxazin-6-one), 2,2'-p-phenylenebis (4-hydro-5-methyl-1,3,6H-oxazin-6-one), 2,2'-m-phenylenebis (4
-Hydro-5-methyl-1,3,6H-oxazine-6
-One) and the like, and 2,2'-bis (3,1-benzoxazin-4-one) is most preferred.

As the benzoxazinone compound, for example, 2,8-dimethyl-4H, 6H-benzo [1,2-
d: 5,4-d '] bis- [1,3] -oxazine-
4,6-dione, 2,7-dimethyl-4H, 9H-benzo [1,2-d: 4,5-d '] bis- [1,3] -oxazine-4,9-dione, 2,8 -Diphenyl-4
H, 8H-benzo [1,2-d: 5,4-d '] bis-
[1,3] -oxazine-4,6-dione, 2,7-diphenyl-4H, 9H-benzo [1,2-d: 4,5-
d '] bis- [1,3] -oxazane-4,6-dione, 6,6'-bis (2-methyl-4H, 3,1-benzoxazin-4-one), 6,6'-bis (2-ethyl-4H, 3,1-benzoxazin-4-one),
6,6'-bis (2-phenyl-4H, 3,1-benzoxazin-4-one), 6,6'-methylenebis (2
-Methyl-4H, 3,1-benzoxazin-4-one), 6,6′-methylenebis (2-phenyl-4H,
3,1-benzoxazin-4-one), 6,6'-ethylenebis (2-methyl-4H, 3,1-benzoxazin-4-one), 6,6'-ethylenebis (2-phenyl- 4H, 3,1-benzoxazin-4-one),
6,6′-butylenebis (2-methyl-4H, 3,1-
Benzoxazin-4-one), 6,6'-butylenebis (2-phenyl-4H, 3,1-benzoxazine-
4-one), 6,6'-oxybis (2-methyl-4
H, 3,1-benzoxazin-4-one), 6,6 ′
-Oxybis (2-phenyl-4H, 3,1-benzoxazin-4-one), 6,6′-sulfonylbis (2
-Methyl-4H, 3,1-benzoxazin-4-one), 6,6′-sulfonylbis (2-phenyl-4)
H, 3,1-benzoxazin-4-one), 6,6 ′
-Carbonylbis (2-methyl-4H, 3,1-benzoxazin-4-one), 6,6′-carbonylbis (2-phenyl-4H, 3,1-benzoxazin-4
-One), 7,7'-methylenebis (2-methyl-4
H, 3,1-benzoxazin-4-one), 7,7 '
-Methylenebis (2-phenyl-4H, 3,1-benzoxazin-4-one), 7,7′-bis (2-methyl-4H, 3,1-benzoxazin-4-one), 7,
7'-ethylenebis (2-methyl-4H, 3,1-benzoxazin-4-one), 7,7'-oxybis (2
-Methyl-4H, 3,1-benzoxazin-4-one), 7,7'-sulfonylbis (2-methyl-4H,
3,1-benzoxazin-4-one), 7,7'-carbonylbis (2-methyl-4H, 3,1-benzoxazin-4-one) and the like, and 2,8-dimethyl-
4H, 6H-benzo [1,2-d: 5,4-d '] bis- [1,3] -oxazine-4,6-dione is most preferred.

The cyclic imino ethers used in the present invention include oxazoline compounds having a 5-membered imino ether ring and oxazine compounds having a 6-membered imino ether ring.

As the oxazoline compound, for example, 2
-Oxazoline, 4-methyl-2-oxazoline, 5-
Methyl-2-oxazoline, 4,5-dimethyl-2-oxazoline, 2,2′-bis (2-oxazoline),
2,2′-bis (4-methyl-2-oxazoline),
2,2′-bis (4-ethyl-2-oxazoline),
2,2'-bis (4,4'-diethyl-2-oxazoline), 2,2'-bis (4-propyl-2-oxazoline), 2,2'-bis (4-butyl-2-oxazoline) 2,2'-bis (4-hexyl-2-oxazoline), 2,2-bis (4-cyclohexyl-2-oxazoline), 2,2'-bis (4-phenyl-2-oxazoline), 2, 2'-bis (4-benzyl-2-oxazoline), 2,2'-o-phenylenebis (2-oxazoline), 2,2'-m-phenylenebis (2-oxazoline), 2,2'-p -Phenylenebis (2-oxazoline), 2,2'-o-phenylenebis (4-methyl-2-oxazoline), 2,2'-m-phenylenebis (4-methyl-2-oxazoline), 2,2 '-P-phenylenebis (4-methyl- - oxazoline), 2,
2'-o-phenylenebis (4,4'-dimethyl-2-
Oxazoline), 2,2'-m-phenylenebis (4,
4'-dimethyl-2-oxazoline), 2,2'-p-
Phenylenebis (4,4'-dimethyl-2-oxazoline), 2,2'-ethylenebis (2-oxazoline),
2,2′-tetramethylenebis (2-oxazoline),
2,2′-hexamethylenebis (2-oxazoline),
2,2-octamethylenebis (2-oxazoline),
2,2-decamethylenebis (2-oxazoline), 2,
2-ethylenebis (4-methyl-2-oxazoline),
2,2'-tetramethylenebis (4,4'-dimethyl-
2-oxazoline), 2,2'-9,9'-diphenoxyethanebis (4,4'-dimethyl-2-oxazoline), 2,2'-cyclohexylenebis (2-oxazoline) and the like. Can be made, but 2,2'-bis (2
-Oxazoline) is most preferred. Examples of the oxazine compound include 1,2-oxazine, 2,2′-bis (5,6-dihydro-4H-1,3-oxazine),
2,2'-methylenebis (5,6-dihydro-4H-
1,3-oxazine), 2,2′-ethylenebis (5,
6-dihydro-4H-1,3-oxazine), 2,2 ′
-Propylene bis (5,6-dihydro-4H-1,3-
Oxazine), 2,2'-butylenebis (5,6-dihydro-4H-1,3-oxazine), 2,2'-hexamethylenebis (5,6-dihydro-4H-1,3-oxazine), , 2'-p-phenylenebis (5,6-dihydro-4H-1,3-oxazine), 2,2'-m-
Phenylenebis (5,6-dihydro-4H-1,3-oxazine), 2,2'-naphthylenebis (5,6-dihydro-4H-1,3-oxazine), 2,2'-p, p
'-Diphenylenebis (5,6-dihydro-4H-1,
3-oxazine), but 2,2 '
-Bis (5,6-dihydro-4H-1,3-oxazine) is most preferred.

The aromatic hydroxycarboxylic acid used in the present invention includes, for example, o-hydroxybenzoic acid, m-hydroxybenzoic acid, p-hydroxybenzoic acid, 1-carboxy-2-hydroxynaphthalene, 1-carboxy-3-
Hydroxynaphthalene, 1-carboxy-4-hydroxynaphthalene, 1-carboxy-5-hydroxynaphthalene, 1-carboxy-6-hydroxynaphthalene, 1
-Carboxy-7-hydroxynaphthalene, 1-carboxy-8-hydroxynaphthalene, 1-hydroxy-2
-Carboxynaphthalene, 1-hydroxy-3-carboxynaphthalene, 1-hydroxy-6-carboxynaphthalene, 1-hydroxy-7-carboxynaphthalene,
2-carboxy-3-hydroxynaphthalene, 2-carboxy-6-hydroxynaphthalene, 2-carboxy-
7-hydroxynaphthalene, 3-carboxy-3'-hydroxybiphenyl, 3-carboxy-4'-hydroxybiphenyl, 3-hydroxy-4'-carboxybiphenyl, 4-carboxy-4'-hydroxybiphenyl and the like can be mentioned.

The polyvalent amine compound used in the present invention is
For example, 1,4-diaminobenzene, 1,3-diaminobenzene, 1,2-diaminobenzene, 2,3-diaminotoluene, 2,4-diaminotoluene, 2,5-diaminotoluene, 2,6-diaminotoluene 1,2-diaminoethane, 1,2-diaminopropane, 1,3-diaminopropane, 1,2-diaminobutane, 1,3-diaminobutane, 1,4-diaminobutane, 1,3-diamino-2 -Methylpropane, 4,4'-diaminobiphenyl, 3,4-diaminobiphenyl, 3,3'-diaminobiphenyl, bis (3-aminophenoxy) methane,
Bis (4-aminophenoxy) methane, bis (3-aminophenoxy) ethane, bis (4-aminophenoxy)
Ethane, 2,2-bis (3-aminophenoxy) propane, 2,2-bis (4-aminophenoxy) propane,
Bis (3-aminophenoxy) ether, bis (4-aminophenoxy) ether, bis (3-aminophenoxy) ketone, bis (4-aminophenoxy) ketone, bis (3-aminophenoxy) sulfone, bis (4-amino Phenoxy) sulfone, bis (3-aminophenoxy) sulfide, bis (4-aminophenoxy) sulfide, bis (3-aminophenoxy) sulfoxide, bis (4-aminophenoxy) sulfoxide, melamine,
1,2,3-triaminobenzene, 1,2,4-triaminobenzene, 1,3,5-triaminobenzene, 1,
2,3-triaminocyclohexane, 1,2,4-triaminocyclohexane, 1,3,5-triaminocyclohexane, 1,2,3-triaminonaphthalene, 1,
2,4-triaminonaphthalene, 1,2,5-triaminonaphthalene, 1,2,6-triaminonaphthalene,
1,2,7-triaminonaphthalene, 1,2,8-triaminonaphthalene, 1,3,5-triaminonaphthalene, 1,3,6-triaminonaphthalene, 1,3,7-
Triaminonaphthalene, 1,3,8-triaminonaphthalene, 1,4,5-triaminonaphthalene, 1,4,6
-Triaminonaphthalene, 1,4,7-triaminonaphthalene, 1,6,7-triaminonaphthalene, 1,6
8-triaminonaphthalene, 2,3,6-triaminonaphthalene, 2,3,7-triaminonaphthalene, 3,3
'-Diaminobenzidine, 1,2,3,4-tetraaminobenzene, 1,2,3,5-tetraaminobenzene,
1,2,4,5-tetraaminobenzene, 3,3 ′,
4,4'-tetraaminophenyl ether, 3,3 ',
4,4'-tetraaminophenylsulfone, 3,3 ',
4,4'-tetraaminophenyl ketone and the like.

The polyhydric alcohols used in the present invention include, for example, ethylene glycol, 1,3-propanediol, 1,2-propanediol, 1,4-butanediol, 1,3-butanediol, 2-butanediol, 1,2-pentanediol, 1,3-pentanediol, 1,4-pentanediol, 1,5-pentanediol, 2,3-pentanediol, 2,4-pentadiol, 1,6 -Hexanediol, 1,5-hexanediol, 1,4-hexanediol, 1,3-hexanediol, 1,2-hexanediol, 2,3-hexanediol, 2,4-hexanediol, 2,5-hexanediol
Hexanediol, 3,5-hexanediol, 1,1
0-decanediol, neopentyl glycol, 2,
2,4-trimethyl-1,3-pentanediol, 3-
Methyl-1,5-pentanediol, 3,3-dimethyl-1,3-propanediol, 1,4-cyclohexanedimethanol, 1,4-benzenedimethanol, polymethylene glycol, polyethylene glycol, polyvinyl alcohol, polyhydroxy Ethyl methacrylate,
Polyhydroxypropyl methacrylate, glycerin,
Trimethylolethane, trimethylolpropane, trimethylolbutane, trimethylolpentane, pentaerythritol, sorbitol, castor oil, hydrogenated bisphenol A, bisphenol dihydroxypropyl ether, 1,3,5-tri (hydroxymethyl) pentane, 1,3, 3,5-tetra (hydroxymethyl) pentane, 1,2,6-trihydroxyhexane, 1,2,2
2,6-tetrahydroxyhexane and the like; and other sugars such as arabinose, ribose, deoxyribose, xylose, glucose, fructose, mannose and galactose, or disaccharides, oligosaccharides and polysaccharides which are condensates thereof. Examples of those having optical activity include D-form, L-form and DL-form.

The epoxy compounds used in the present invention include ethylene oxide, propylene oxide, butylene oxide, styrene oxide, butyl glycidyl ether, allyl glycidyl ether, phenyl glycidyl ether, epichlorohydrin, cyclohexane vinyl monoxide, dipentene monoxide. Cresyl glycidyl ether, α-pinene oxide, glycidyl methacrylate, butadiene monoepoxide, 1,2-epoxy-7-octene, glycidyl acrylate, glycidyl undecylate, methyl vinyl glycidylamine, vinyl-3,4-epoxycyclohexane, Allyl-3,
4-epoxycyclohexane, 3,4-epoxycyclohexyl acrylate, 2,3-epoxypropyl-4
-Vinylphenyl ether, 2,3-epoxycinnamyl acrylate, 9,10-epoxyoleyl acrylate, 2,3-epoxybutyl methacrylate, methyl glycidyl methacrylate, bisphenol A glycidyl ether, ethylene glycol diglycidyl ether, 1,4-butane Diol diglycidyl ether, aryl glycidyl ether, 3,4-epoxycyclohexylmethyl methacrylate, glycerol diglycidyl ether, ethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, resorcin diglycidyl ether, neopentyl glycol diglycidyl ether, 1,6 -Hexanediol diglycidyl ether, hydroquinone diglycidyl ether, bisphenol S Glycidyl ether, diglycidyl adipate, diglycidyl o-phthalate, diglycidyl terephthalate, sorbitol polyglycidyl ether, sorbitan polyglycidyl ether, polyglycerol polyglycidyl ether, pentaerythritol polyglycidyl ether, diglycerol polyglycidyl ether Tri, methylolpropane polyglycidyl ether, polyethylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, polytetramethylene glycol diglycidyl ether and the like. Among these epoxy compounds, glycidyl acrylate and glycidyl methacrylate are particularly preferred from the viewpoint of ease of handling, low cost, miscibility, and low vapor pressure.

Examples of the polyfunctional aziridine compound used in the present invention include 2,2-bishydroxymethylbutanol tris [3- (1-aziridinyl) propionate] and ethylene glycol-bis [3- (1-aziridinyl) Propionate], polyethylene glycol-
Bis- [3- (1-aziridinyl) propionate],
Propylene glycol-bis [3- (1-aziridinyl) propionate], polypropylene glycol-bis [3- (1-aziridinyl) propionate], tetramethylene glycol-bis [3- (1-aziridinyl) propionate], polytetramethylene glycol -Bis [3- (1-aziridinyl) propionate] and the like.

The lactams used in the present invention include:
For example, ε-caprolactam, ω-laurolactam, 2
-Pyrrolidone, 2-piperidone, 2-azacyclobutanone, 2-azacyclooctanone, 2-azacyclononanone, glycosiamidine, oxindole, isatin,
N, N'-terephthalyl biscaprolactam and the like.

The lactones used in the present invention include:
For example, glycolide, lactide, 1,4-dioxanone, ε-caprolactone, 1,5-dioxysepan 2-
ON, trimethylene carbonate, β-butyrolactone, β-propiolactone, δ-valerolactone, γ-
Butyrolactone, enantholactone, caprylolactone, β-methylpropiolactone, β-dimethylpropiolactone, δ-caprolactone, ethylene oxalate, ethylene malonate, ethylene succinate, ethylene adipate, propylene oxalate, propylene malonate, Propylene succinate, propylene adipate, tetramethylene oxalate, tetramethylene malonate, tetramethylene succinate, tetramethylene adipate, ｛o-α-D-glucopyranosyl-
(1 → 4)｝ 4-D′-glucono-1,5-lactone,
β-methyl-δ-valerolactone and the like. In addition, diethylene glycol bischloroformate is effective as a thickener.

Examples of the alkaline earth metal compound used in the present invention include magnesium oxide, calcium oxide, calcium hydroxide, magnesium hydroxide, magnesium silicate, calcium silicate, and other silicates.

Examples of the alkali metal salts include sodium polyacrylate, potassium polyacrylate, lithium polyacrylate, sodium polymethacrylate, potassium polymethacrylate, polylithium methacrylate, sodium alginate, potassium alginate, lithium alginate and the like. Can be

Examples of the water-soluble polymer include Noritsugi, Laponite, oxide, troloioi, gluten, and belowoi.

In addition, examples of the thermoplastic resin include an acrylic resin, polyisobutylene, an ethylene-propylene copolymer, a styrene-diene block copolymer, a carboxyl-containing vinyl copolymer, and a polyalkyl methacrylate.

Other examples include natural rubber, cellulose derivatives such as carboxymethylcellulose and hydroxyethylcellulose, starch, boric acid, borax, glyoxal,
Terephthalyl bis, bis-okgoloid, hydroxysilky, polyol ester, p-toluenesulfonic acid, radical generator and the like also have an effect as a thickener.

[Addition amount of thickener] The addition amount of the thickener is in the range of 0.01 to 20 parts by weight based on 100 parts by weight of the polylactic acid resin. Preferably, it is in the range of 0.1 to 15 parts by weight, more preferably 1 to 10 parts by weight. If it is less than 0.01 part by weight, the effect as a thickener is not sufficient. If it exceeds 20 parts by weight, depending on the type of the thickener, the viscosity may be too high to be melt-molded.

[Types of Decomposition Type Blowing Agent] Examples of the decomposition type blowing agent used in the present invention include inorganic blowing agents such as sodium bicarbonate, and the like.
Organic foaming agents such as azodicarbonamide, N, N'-dinitropentamethylenetetramine, p, p'-oxybis (benzenesulfonylcarbazide), azobisisobutyronitrile and benzenesulfonylhydrazide.

[Addition amount of decomposable foaming agent] The amount of the decomposable foaming agent added is 0.1 to 100 parts by weight of the polylactic acid resin.
It is in the range of ２０20 parts by weight. Preferably, 0.5 to 10
Parts by weight, more preferably 0.8 to 5 parts by weight. If the amount is less than 0.1 part by weight, the effect as a decomposition-type foaming agent is not sufficient. If the amount exceeds 20 parts by weight, poor appearance may be caused.

[Polylactic acid-based resin] The polylactic acid-based resin in the present invention refers to polylactic acid alone, a copolymer of polylactic acid and an aliphatic polyester, or a blend or alloy of polylactic acid and an aliphatic polyester.

[Polylactic acid] In the present invention, specific examples of the lactic acid as a raw material of the polylactic acid include L-lactic acid, D-lactic acid, DL-lactic acid or a mixture thereof, or a cyclic dimer of lactic acid. Lactide can be mentioned. Specific examples of the method for producing polylactic acid used in the present invention include, for example, a method of directly dehydrating polycondensation using lactic acid or a mixture of lactic acid and an aliphatic hydroxycarboxylic acid (for example, US Pat. No. 5,310,865). ), A ring-opening polymerization method for melt-polymerizing a cyclic dimer of lactic acid (lactide) (for example, a production method disclosed in US Pat. No. 2,758,987), lactic acid and fat A cyclic dimer of an aromatic hydroxycarboxylic acid,
For example, a ring-opening polymerization method in which lactide or glycolide and ε-caprolactone are melt-polymerized in the presence of a catalyst (for example, a production method disclosed in US Pat. No. 4,057,537), lactic acid, aliphatic divalent A method of directly dehydrating and polycondensing a mixture of an alcohol and an aliphatic dibasic acid (for example, a production method disclosed in US Pat. No. 5,428,126); a polylactic acid, an aliphatic dihydric alcohol and an aliphatic dibasic A method of condensing a polymer with an acid in the presence of an organic solvent (for example, a production method disclosed in European Patent Publication No. 0712880 A2) can be mentioned, but the production method is not particularly limited. Further, a small amount of an aliphatic polyhydric alcohol such as glycerin, an aliphatic polybasic acid such as butanetetracarboxylic acid, and a polyhydric alcohol such as a polysaccharide may coexist and may be copolymerized. The molecular weight may be increased by using a binder (polymer chain extender) such as a diisocyanate compound.

[Aliphatic polyester] The polylactic acid in the present invention may be a copolymer or a blend with an aliphatic polyester, if necessary. Aliphatic polyesters are biodegradable polymers that can be produced by various combinations of aliphatic hydroxycarboxylic acids, aliphatic dihydric alcohols and aliphatic dibasic acids. As a method for producing a copolymer with an aliphatic polyester or polylactic acid,
A method similar to the method for producing polylactic acid can be used, but is not limited thereto.

[Aliphatic hydroxycarboxylic acid] Specific examples of the aliphatic hydroxycarboxylic acid include glycolic acid,
Examples thereof include 3-hydroxybutyric acid, 4-hydroxybutyric acid, 3-hydroxyvaleric acid, 4-hydroxyvaleric acid, and 6-hydroxycaproic acid. Further, cyclic esters of aliphatic hydroxycarboxylic acids, for example, glycolic acid Examples include glycolide which is a dimer and ε-caprolactone which is a cyclic ester of 6-hydroxycaproic acid. These can be used alone or in combination of two or more.

[Aliphatic dihydric alcohol] Specific examples of the aliphatic dihydric alcohol include, for example, ethylene glycol, diethylene glycol, triethylene glycol,
Polyethylene glycol, propylene glycol, dipropylene glycol, 1,3-butanediol, 1,4
-Butanediol, 3-methyl-1,5-pentaneddiol, 1,6-hexanediol, 1,9-nonanediol, neopentyl glycol, polytetramethylene glycol, 1,4-cyclohexanedimethanol, 1,
4-benzenedimethanol and the like. They are,
They can be used alone or in combination of two or more.

[Aliphatic dibasic acid] Specific examples of the aliphatic dibasic acid include, for example, succinic acid, oxalic acid, malonic acid,
Glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, undecandioic acid, dodecandioic acid, phenylsuccinic acid, 1,4-phenylenediacetic acid, and the like. These can be used alone or in combination of two or more. In the present invention, the aliphatic polyester is a biodegradable fat having a melting point of 40 ° C to 250 ° C, which can be produced by variously combining the above-described aliphatic hydroxycarboxylic acid, aliphatic dihydric alcohol and aliphatic dibasic acid. There is no restriction as long as it is a group III polyester. Particularly, a soft aliphatic polyester having crystallinity is preferable. When the melting point of the aliphatic polyester is lower than 40 ° C., the heat resistance of the obtained polylactic acid-based resin composition is reduced, and when the melting point is higher than 250 ° C., the melting temperature during pelletization is increased, so that the polylactic acid component is deteriorated. It is not preferred because it tends to be colored. Preferred aliphatic polyesters include polyethylene oxalate, polybutylene oxalate, polycaprolactone, polyneopentyl glycol oxalate, polyethylene succinate, polybutylene succinate, polyhydroxybutyric acid and β-hydroxybutyric acid and β-hydroxyvaleric acid. And particularly preferred are polyethylene succinate and polybutylene succinate.

These aliphatic polyesters may have a polymer chain extended by a binder such as diisocyanate, or may be a small amount of an aliphatic polyhydric alcohol such as glycerin or butanetetracarboxylic acid. Polyhydric alcohols such as aliphatic polybasic acids and polysaccharides may coexist and be copolymerized. The weight average molecular weight (Mw) and molecular weight distribution of polylactic acid and aliphatic polyester are not particularly limited as long as they can be substantially molded. The weight average molecular weight of the polylactic acid and the aliphatic polyester used in the present invention is not particularly limited as long as it shows substantially sufficient mechanical properties, but is generally 1 to 5 in weight average molecular weight (Mw). 1,000,000 is preferred, and 3 to
500,000 is more preferable, and 50,000 to 300,000 is further preferable.
In general, when the weight average molecular weight (Mw) is less than 10,000, the mechanical properties of the foamed molded article obtained are insufficient, and when the molecular weight exceeds 1,000,000, handling becomes difficult. , It can be uneconomical.

[Foam Extrusion Molding] As a foam extrusion apparatus used to obtain a foam or a foam sheet by extrusion foam molding, a single-screw extruder, a twin-screw extruder, and a tandem-type foaming apparatus having two single-screw units connected to each other. Extrusion equipment is mentioned. For the production of the foam and the foamed sheet of the present invention, a tandem type foam extruder is more preferable in terms of efficiency.

The screw used for the extruder may be a screw used for ordinary extrusion molding, and the L / D is usually good in the range of 28 to 35.

The die used in the extruder may be any one of circular dies, capillary dies, T dies, and the like, depending on the desired foam shape. Land length is usually
The range is 5 to 100 mm. Die pressure is usually 2-10
MPa range. Die temperature is typically 130-150
It is in the range of ° C. The extruder is usually fitted with a gas leakage prevention ring. The cylinder temperature near the ring is 17
It is essential that the resin is completely melted at about 0 to 200 ° C.

The extrusion temperature depends on the type and molecular weight of the polylactic acid-based resin composition to be used and the type and amount of the thickener.
It is in the range of 50-250 ° C. More preferably 160 ~
The range is 230 ° C, most preferably 170-200 ° C. It is preferable that the resin extruded from the die be rapidly cooled at the time of foaming to prevent dissipation of the foaming agent. For this purpose, it is desirable to install a cooling device after the extruder, and the cooling is performed by a method of blowing air or the like, a method of passing the same through water, a method of spraying them, or the like. The extruded foam can be wound into a roll by installing a mandrel, a cutter, a take-up machine and a take-up machine.

[Other Additives] In the present invention, a lubricant, a filler, a coloring agent, a plasticizer, an ultraviolet absorber, an antioxidant and the like may be added if the purpose is not impaired.

[Foam Sheet] The foam sheet obtained in the present invention can be subjected to secondary processing such as vacuum forming, pressure forming, and vacuum forming.

[0055]

The present invention will be described in detail with reference to the following examples, but it should not be construed that the invention is limited thereto without departing from the technical scope of the present invention. The weight average molecular weight (Mw) of the polylactic acid-based resin, the shapeability in the examples, and the strength were measured by the following methods.

Weight average molecular weight (Mw) Measured by gel permeation chromatography (GPC) using a polystyrene as a standard and a column temperature of 40 ° C. in a chloroform solvent.

The brittleness of the foam molded article was classified as follows.・ ・ ・: Strong △: Slightly brittle ×: Brittle

Production Example 1 400 g of L-lactide and stannous octoate
04 g and lauryl alcohol 0.12 g were sealed in a thick cylindrical stainless steel polymerization vessel equipped with a stirrer and degassed under vacuum for 2 hours. After replacing with nitrogen gas, 200 ℃
The mixture was heated and stirred at / 10 mmHg for 2 hours. After completion of the reaction, a melt of polylactic acid was extracted from the lower outlet, air-cooled, and cut with a pelletizer. The resulting polylactic acid had a yield of 340 g, a yield of 85%, and a weight average molecular weight (M
w) 138,000.

Production Example 2 9 reactor was equipped with a Dien-Stark trap.
10 kg of 0% L-lactic acid and 45 g of tin powder are charged, and 150 ° C.
After distilling water while stirring at / 50 mmHg for 3 hours, the mixture was stirred at 150 ° C / 30 mmHg for 2 hours to oligomerize. 21.1 kg of diphenyl ether was added to this oligomer, and an azeotropic dehydration reaction at 150 ° C./35 mmHg was performed. The distilled water and the solvent were separated by a water separator, and only the solvent was returned to the reactor. Two hours later, the organic solvent to be returned to the reactor was passed through a column packed with 4.6 kg of molecular sieve 3A, and then returned to the reactor.
The reaction was carried out at 17 mmHg for 20 hours to obtain a polylactic acid solution having a weight average molecular weight (Mw) of 150,000. 44 kg of dehydrated diphenyl ether was added to this solution to dilute it, and then cooled to 40 ° C., and the precipitated crystals were filtered. 12 kg of 0.5 N HCl and 12 k of ethanol
g, and the mixture was stirred at 35 ° C. for 1 hour, and then filtered.
Drying at 50 mmHg yielded 6.1 kg of polylactic acid powder (85% yield). This powder was melted and pelletized by an extruder to obtain polylactic acid. The weight average molecular weight (Mw) of this polymer was 1470,000.

Production Example 3 In a reactor equipped with a Dien-Stark trap,
50.5 kg of 1,4-butanediol and succinic acid
After 5 kg of tin powder and 45 g of tin powder were charged, water was distilled off while stirring at 100 ° C. for 3 hours, and the mixture was further stirred at 150 ° C./50 mmHg for 2 hours to oligomerize. 385 kg of diphenyl ether is added to this oligomer,
An azeotropic dehydration reaction of 5 mmHg was performed, and the distilled water and the solvent were separated by a water separator, and only the solvent was returned to the reactor. Two hours later, the organic solvent to be returned to the reactor was passed through a column filled with 50 kg of molecular sheep 3A, and then returned to the reactor. The reaction was carried out at 130 ° C./17 mmHg for 15 hours, and the weight average molecular weight (Mw) was obtained. 14,000 polybutylene succinate (hereinafter abbreviated as PSB) solution was obtained. After 180 kg of dehydrated diphenyl ether was added to this solution for dilution, the solution was cooled to 40 ° C., and the precipitated crystals were filtered. To this powder were added 200 kg of 0.5 N HCl and 200 kg of ethanol, and the mixture was stirred at 25 ° C. for 1 hour, filtered, dried at 60 ° C./50 mmHg, and dried with PSB 91.
5 kg (94.8% yield) were obtained. The weight average molecular weight (Mw) of this PSB was 138,000.

Examples 1 to 4 and Comparative Example 1 As shown in Table 1, a polylactic acid-based resin, a thickener and a foaming agent were mixed using a Henschel mixer, and were melt-kneaded using a single screw extruder. The cylinder temperature was 170 to 180 ° C, the temperature near the gas leakage prevention ring was 180 ° C, and the temperature of the T-die was 140 ° C. The resin kneaded material was discharged into the atmosphere from the slit to obtain a foamed sheet having a width of 650 mm. The expansion ratio and brittleness of the obtained sheet were evaluated. The results are summarized in Table 1 (Table 1).

[0062]

[Table 1] HDI: Hexamethylene diisocyanate

[0063]

The composition for producing a polylactic acid-based resin foam of the present invention is suitable for foam molding and improves the expansion ratio. The obtained molded article and sheet have improved foam moldability as compared with conventional polylactic acid.

 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Takayuki Watanabe 1190 Kasama-cho, Sakae-ku, Yokohama-shi, Kanagawa Prefecture (72) Inventor Hisashi Aihara 1190 Kasama-cho, Sakae-ku, Yokohama-shi, Kanagawa Mitsui Chemicals ( 72) Inventor Tomoyuki Nakata 1190 Kasama-cho, Sakae-ku, Yokohama-shi, Kanagawa Prefecture F-term (reference) 4F074 AA68 AC19 AC33 AD13 AG20 BA01 BA13 CA22 DA02 DA08 4J029 AA02 AA03 AB07 AC01 AC02 AD01 AD06 AD10 AE03 AE18 BA02 BA03 BA05 BA07 BA08 BA09 BA10 BB06A BD07A BF09 BF10 BF18 BF25 CA01 CA02 CA03 CA04 CA05 CA06 CA09 EA02 EA03 EA05 EG09 EH01 EH02 FC03 FC14 HA01 HB01 JA093 JA283 J303 JB123 JB163 JB173 JBJC JB173 JB183 JBC JB273 JBC3 JC373 JD05 JE012 JE013 JE023 JE033 JE043 JE053 JE083 JE093 JE153 JE163 JE1 82 JE183 JF133 JF143 KE05 KE09 KH01 KH08

Claims (8)

[Claims] 1. (A) 100 parts by weight of a polylactic acid-based resin, based on 100 parts by weight of a polylactic acid-based resin, (B)
A composition for producing a polylactic acid-based resin foam, comprising 0.01 to 20 parts by weight of a thickener and 0.1 to 20 parts by weight of a decomposition type foaming agent (C). 2. (A) 100 parts by weight of a polylactic acid-based resin based on 100 parts by weight of a polylactic acid-based resin; and
(B) a resin composition containing 0.01 to 20 parts by weight of a thickener, and (C) 0.1 to 20 parts by weight of a decomposable foaming agent. A composition for producing a polylactic acid-based resin foam. 3. (A) 100 parts by weight of a polylactic acid-based resin based on 100 parts by weight of a polylactic acid-based resin, and (B)
A polylactic acid-based resin obtained by melt-foam molding a composition containing 0.01 to 20 parts by weight of a thickener and 0.1 to 20 parts by weight of a decomposable foaming agent. A method for producing a foam. 4. A polylactic acid-based resin (A) 100 parts by weight, based on (A) a polylactic acid-based resin 100 parts by weight, and
(B) A resin composition containing 0.01 to 20 parts by weight of a thickener and (C) a composition containing 0.1 to 20 parts by weight of a decomposable foaming agent are melt-foamed. A method for producing a polylactic acid-based resin foam. 5. A polylactic acid-based resin based on 100 parts by weight of (A) a polylactic acid-based resin, and
(B) When melt-molding a resin composition containing 0.01 to 20 parts by weight of a thickener, (C) a decomposition type foaming agent of 0.1
A method for producing a polylactic acid-based resin foam, comprising adding to 20 parts by weight and foaming. 6. A method for producing a polylactic acid-based foam, comprising subjecting the composition according to claim 1 or 2 to melt foam molding. 7. A polylactic acid-based foam obtained by the production method according to claim 3. 8. A polylactic acid-based foamed sheet obtained by the production method according to claim 3.