JP2003119276A - Method for producing polylactic acid resin excellent in thermal stability - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a method for producing a polylactic acid which inhibits a depolymerization reaction and the like during thermoforming, gives a stable formed article and suppresses deterioration with time of a formed article. SOLUTION: The method for producing a formed product of a polylactic acid resin excellent in thermal stability during forming comprises washing a polylactic acid mainly composed of a lactic acid with a solvent which dissolvers a lactic acid monomer, a cyclic dimmer and a polymerization catalyst thereby reducing the residual monomer to at most 1% and the residual catalyst to at most 0.01% in the polymer, and carrying out forming with at least 0.05% of a thermal stabilizer added.

Description

Detailed Description of the Invention

[0001]

FIELD OF THE INVENTION The present invention relates to a method for producing a polylactic acid resin having excellent thermal stability. In particular, it relates to a method for producing a resin having excellent thermal stability during molding.

[0002]

2. Description of the Related Art Biodegradable polymers which are decomposed by microorganisms have been attracting attention in recent years from the viewpoint of environmental protection. For example, polyhydroxybutyrate (PHB) and polycaprolactone (PCL) are known as biodegradable polymers that can be melt-molded. However, PHB not only has an excessively high manufacturing cost but also has a transparency of a molded product. Inferiorly, the melting point of PCL is too low at 60 ° C., which is a serious problem and obstacle in practical use.

Polylactic acid is expected to be a biodegradable polymer which has a relatively low cost, a melting point of 170 ° C. or higher and sufficient heat resistance, is melt-moldable and is practically excellent. However, conventionally obtained polylactic acid is inferior in melt moldability,
Moreover, the obtained molded products, films, fibers, etc. have the serious drawbacks of low toughness, brittleness and weakness.

The present inventors have previously proposed a method for producing polylactic acid having good physical properties and biodegradability as a molding material that compensates for the conventional defects. However, if a polylactic acid polymerization catalyst or a lactic acid monomer or oligomer remains during molding of polylactic acid, a depolymerization reaction occurs during heat molding, which causes a decrease in molecular weight and coloring. In addition, if the monomer or oligomer remains, the physical properties of the molded product deteriorate with time, which is a major instability factor in the manufacture and use of various products.

The present inventors have completed the present invention as a result of extensive studies on the cause and countermeasures. That is, the object of the present invention is a method for producing a polylactic acid resin for suppressing depolymerization reaction or the like during heat molding, producing a stable molded article, and suppressing deterioration of the molded article over time. To suggest.

[0006]

[Means and Actions for Solving Problems] According to the present invention, polylactic acid containing lactic acid as a main component is washed with a solvent that dissolves a lactic acid monomer, a cyclic dimer and a polymerization catalyst to obtain an amount of residual monomer in the polymer. At least 1%, the amount of residual catalyst is at most 0.01%, and the heat stabilizer is at least 0.0 at the time of molding.
A method for producing a polylactic acid resin, which comprises adding 5% and molding.

The lactic acid used in the present invention preferably has a lactic acid component of at least 85% by weight, more preferably 99.7.
˜90% by weight, particularly preferably 99.5 to 92% by weight. If the lactic acid component is less than 85% by weight, the crystallinity of the produced polymer is too low and practical heat resistance and strength cannot be obtained, which may cause a problem in use.

Lactic acid has an optically active carbon atom, and L-
It has a body and a D-body. The product generally obtained by the fermentation method has a large amount of L-form and is produced at low cost. In addition, the L-form is preferred because it is easily decomposed by microorganisms after use, but is not particularly limited. Further, a mixture of L-form and D-form can be used, but if the mixing ratio is large, it causes problems in producing a product such as a decrease in melting point and a decrease in mechanical strength. Usually, the proportion of L-form (or D-form) in polylactic acid is at least 80%, preferably at least 85%, more preferably at least 90%.

The monomer copolymerizable with polylactic acid is not limited as long as it is a compound having a functional group that reacts with a hydroxyl group or a carboxyl group of lactic acid, but is preferably a medium or high molecular weight polyethylene glycol (hereinafter abbreviated as PEG). ), Polypropylene glycol, poly (ethylene /
Propylene) glycol and other polyalkylene glycols (hereinafter abbreviated as PAG), polyethylene adipate,
Use of aliphatic polyesters such as polybutylene adipate and polyethylene sebacate, bisphenol compounds having a polyethylene glycol segment or polypropylene segment in the molecular structure, or polylactones such as polycaprolactone and polyhyvalolactone, and cyclic polyester compounds such as caprolactone and hyvalolactone. Is possible. The molecular weight per terminal hydroxyl group or carboxyl group is preferably 300 or more, more preferably 1000 or more, and particularly preferably 3000 to 20.
It is 000.

The copolymerization ratio of the copolymerization components (weight ratio in the copolymer) is preferably at most 15%, more preferably 0.3 to 10%, particularly preferably 0.5 to 8%. When the copolymerization ratio is higher than 15%, the polylactic acid copolymer obtained is flexible and the melting point is lowered, the degree of polymerization is hard to increase, and it becomes difficult to maintain practical strength and heat resistance. The decrease of the melting point of polylactic acid or polylactic acid copolymer is caused by the hydroxyl group or carboxyl group of the copolymerization monomer.
The larger the molecular weight per square, the smaller. Therefore, when using a copolymerizable monomer having a low molecular weight, it is not preferable to increase the copolymerization ratio too much. For example, when the molecular weight per hydroxyl group of the copolymerization monomer is 1000, it is about 0.3 to 10%, and the molecular weight per hydroxyl group is 3000.
In this case, a copolymerization ratio of about 0.5 to 15% is preferable.

The polymerization mechanism of polylactic acid is an acid / alcohol reaction between a hydroxyl group and a carboxyl group, and the degree of polymerization is highest when the numbers of both are the same. Therefore, it is also preferable to add to the polymerization reaction system a dicarboxylic acid component that is substantially equimolar to the terminal hydroxyl group of the PAG component in order to keep the molar balance between the carboxylic acid and the hydroxyl group in the polymerization system constant. That is, "substantially equimolar" means that the molar ratio of the carboxylic acid and the hydroxyl group is 0.
It is preferable to maintain the range of 9 to 1.1, particularly 0.95 to 1.05.

Examples of the dicarboxylic acid component used in the present invention include adipic acid, sebacic acid, decanedicarboxylic acid and the like, aliphatic dicarboxylic acids having about 4 to 12 carbon atoms, isophthalic acid, terephthalic acid, naphthalenedicarboxylic acid and the like. Aromatic dicarboxylic acids, their acid anhydrides, acid halides and low molecular alcohol esters such as methanol esters and ethylene glycol esters of these acids are available. For example, at a stage where the polymerization has progressed to some extent (middle or final stage), an appropriate amount of phthalic anhydride can be added and mixed to react with hydroxyl groups at the ends of two molecular chains to effectively increase the molecular weight. .

The PAG component and the dicarboxylic acid may be added to the reaction system separately, but they are previously reacted (polymerized).
After being at most a polyetherester, it can be reacted with lactic acid, lactide and / or polylactic acid.
This method is also useful in that the dicarboxylic acid component is added to the polymerization system and reacted. Similarly, an oligomer of polyester having a large number of carboxyl groups, which was prepared by reacting an excess amount of dicarboxylic acid with respect to a diol, for example, hexa hexa prepared at a molar ratio of hexanediol / adipic acid of 1/2, 2/3, 3/4, etc. Methylene adipate oligomers can also be used.

The copolymer of the present invention can be copolymerized with a third component in addition to the polylactic acid which is the main component and the PAG component. The copolymerization of the dicarboxylic acid component for balancing the hydroxyl group of the PAG component has already been described.
In addition, for example, the third component can be copolymerized for enhancing or reducing biodegradability, improving dyeability, and the like. For example, by copolymerizing a compound having a sulfonic acid group, for example, sulfoisophthalic acid (or a metal salt thereof),
It can be dyeable with a basic dye, and can be dyed with an acid dye by copolymerizing a compound having an amino group or an amide group, for example, an amino acid.
Since the copolymerization of these third components tends to lower the melting point of the copolymer, it is necessary to perform it carefully while keeping the melting point at 110 ° C or higher.

The molecular weight of the polylactic acid or polylactic acid copolymer of the present invention is remarkably higher than that of the conventionally proposed products.
The toughness of molded products (including films and fibers) is excellent. The molecular weight (Mw) is usually 60 in terms of heat resistance, toughness, fluidity during melting, and molding of molded products (including films and fibers).
000 or more, preferably 80,000 to 300,000, and more preferably 100,000 to 200,000.

As the catalyst used in the polymerization reaction, those usually used for the polymerization of lactic acid and lactide can be used. For example, alcoholates of Na and Mg with various alcohols, Zn, Cd, Mn, Co, Ca, Sb, S
n, Ba and other fatty acid salts, carbonates, sulfates, phosphates,
Oxides such as Mg, Pb, Zn, Sb, Sn, and Ge, hydroxides, halides, or their metals can be used, but not only the catalytic function, but also the product does not form coloring, side reaction, or aggregated foreign matter. Select in consideration of such factors. The amount of catalyst is usually 10 ^-2 to 1 relative to the amount of ester.
Although it is 0 ^-4 mol / mol, it is appropriately selected depending on the temperature and the reaction system. Of course, other than the above, the reaction rate is high,
It is possible to use any one that is excellent in that it has little coloration or side reaction.

In order to improve the chemical stability and thermal stability of the polylactic acid or polylactic acid copolymer, the polymerization system is added with 30 p
It is also preferable to add an antioxidant of about pm to 0.3%, especially 50 ppm to 0.1%. If an antioxidant is used in an excessively large amount, the polymerization may be hindered, and it is desirable that the amount used is the minimum necessary during the polymerization. However, in order to increase the stability of the obtained product, it is possible to additionally mix a large amount of antioxidant, for example, about 0.1 to 3% at the time when the polymerization of the polylactic acid / PAG component copolymer proceeds. I can.

When melt-polymerizing lactide, a part of the monomer (lactide) and a low molecular weight substance (oligomer) may remain in the polymerization system due to the reaction equilibrium of the monomer / polymer. If this residual monomer or low molecular weight oligomer is present in the final product (molded product, film, fiber, etc.), 1
It acts as a kind of plasticizer or as a trigger for hydrolysis, impairing the quality such as coloring of the product, or leaching out during the manufacturing process or use, causing troubles or causing deterioration of strength over time. Therefore, residual low molecular weight compounds (molecular weight 500
The following) is preferably 10% or less, more preferably 5% or less, particularly preferably 3% or less, and most preferably 1% or less. To reduce residual monomers and low molecular weight substances,
To remove them by raising the degree of vacuum in the middle to latter stages of polymerization, polymerization initiator (alcohols such as ethylene glycol, glycerol, propylene glycol and PEG, polypropylene glycol also act as initiators), polymerization catalyst It is also effective to reduce the residual monomer by reacting with the monomer by adding and mixing.

When a large amount of a lactic acid monomer or a dimer or oligomer of lactic acid remains in polylactic acid or a polylactic acid copolymer, the polylactic acid or the polylactic acid copolymer is generated due to the hydroxyl groups or the hydroxyl groups generated by hydrolysis. The molecular weight of the polymer may decrease. Further, if the polylactic acid polymerization catalyst remains, the depolymerization reaction during heating and melting lowers the molecular weight and causes coloration of the polymer. Therefore, it is necessary to reduce the residual lactic acid monomer, dimer or oligomer of lactic acid, and the polymerization catalyst to a certain amount.

The residual monomers include lactic acid monomers, cyclic dimers of lactic acid or linear or cyclic oligomers of lactic acid, the amount of which is at most 1% by weight, preferably at most 0.5% by weight, More preferably, it is 0.1% by weight. If the residual monomer content exceeds 1%, the physical properties of polylactic acid itself and its change over time will be large, and it will cause the generation of monomers and malodor during molding, and also cause foreign matter and whitening in the fibers and molded products.

The amount of residual polymerization catalyst is at most 0.01%, preferably at most 0.007%, more preferably at most 0.0.
It is 05%. When the amount of the residual polymerization catalyst exceeds 0.01%, the decrease in the molecular weight during heat molding becomes large.

As a method for removing the lactic acid monomer, dimer, oligomer and polymerization catalyst remaining in the polylactic acid or the polylactic acid copolymer, it is preferable to dissolve and remove them with a solvent common to both. As the common solvent, for example, a ketone solvent such as ketone, methyl ethyl ketone, methyl isobutyl ketone, methyl acetate, ethyl acetate, methyl lactate,
Examples thereof include ester solvents such as ethyl lactate, carbonate ester solvents such as dimethyl carbonate and diphenyl carbonate, and aromatic solvents such as benzene, toluene and xylene. Preferred is a mixed solvent containing a small amount of strong acid or weak acid such as hydrochloric acid, nitric acid, phosphoric acid or oxalic acid in the above solvent.
The acid concentration is preferably 0.001 N to 1 N in terms of handling.

As a method of dissolving and removing, a method of dipping and stirring in a solvent, a method of passing the solvent through a shower, or the like can be used. Next, the solvent in the polymer is removed by ventilation drying, drying with heated air, or vacuum drying. Although it may be heated to some extent when it is dipped in a solvent or dried, care should be taken so that polylactic acid does not dissolve or stick. In addition, fine powder generated by the washing treatment may adhere to the dried polymer, and therefore caution is required before use. Preferably, it is removed by a cyclone or the like.

By removing the above-mentioned monomers and dimers or various oligomers and catalysts by washing, the heat resistance of polylactic acid is dramatically improved. As a measure of heat resistance, the temperature at which the weight loss rate of a sample reaches 5% by thermal decomposition (eg, TG meter) when heated in nitrogen at a heating rate of 10 ° C./min (hereinafter abbreviated as Td (5%)). However, the melting point of the polylactic acid is higher than the melting point of the polylactic acid by at least 50 ° C. More preferably, it is at least 70 ° C. higher than the melting point of polylactic acid,
Particularly preferably, it is at least 90 ° C higher. Td
When (5%) is less than 50 ° C than the melting point of polylactic acid, polylactic acid is easily decomposed during molding when the molding temperature is raised to increase the fluidity of the polymer, and conversely molding is performed to suppress the decomposition of the polymer. If the temperature is lowered, the viscosity of the polymer at the time of molding becomes too high, and good moldability and molded products cannot be obtained.

By washing, various stabilizers such as a heat stabilizer and a light stabilizer are removed at the same time as the removal of the residual monomer and the residual catalyst, and the thermal stability of the polylactic acid resin at the time of molding is extremely lowered. Therefore, in molding polylactic acid having a high degree of polymerization, melting at a temperature as high as 50 ° C. or more from the melting point of the polymer is usually performed. At that time, the polymer is decomposed, which causes serious problems in terms of quality and operability, such as yarn breakage due to the generation of monomers, contamination of the film, perforation and malodor. Further, when the monomer generated during molding remains in the product or the fiber, there is a demerit as a product quality such as deterioration of physical properties and deterioration of transparency of the molded product or fiber over time.

Accordingly, at the time of molding, the amount of the polymer heat stabilizer is at least 0.05% by weight, preferably 0.1% by weight, more preferably 0.2% by weight or more and 1% by weight or less based on the polylactic acid. Add as much as possible. The amount of heat stabilizer is 0.0
If it is less than 5% by weight, the melt stability of polylactic acid is poor, and the decomposition of polylactic acid causes the generation of monomers, low-molecular compounds, oligomers, etc., which causes deterioration of the operability and the quality of molded products. Further, it is also preferable to add a light stabilizer, a fluidizing agent and the like which are usually used.

As the heat stabilizer used in the present invention, it is possible to use an ordinary polyester resin, a polycarbonate resin, a polyolefin resin or the like used in molding. For example, one or more heat stabilizers such as hindered phenol compounds, hindered amine compounds, arylamine compounds, phosphite compounds and thioester compounds can be used. For the hindered phenol type, for example, there is the “Irganox” series manufactured by Ciba Geigy, and for the hindered amine type, there is the “Tinubin” series. Further, a heat stabilizer such as "Sumilyzer" series can be used as a phenolic antioxidant of Sumitomo Chemical Co., Ltd. Examples of the antioxidants other than those mentioned above include thioether-based ones, and it is often preferable to use two or more kinds of the above stabilizers in combination. Further, from the viewpoint of heat resistance of the heat stabilizer itself, those having a large molecular weight and a high boiling point or sublimation temperature are preferable. For example, the molecular weight is preferably 500 or more, and most preferably 70.
It is 0 or more. The aforementioned Irganox 1010 (molecular weight 1178) is one of the most preferable examples. Examples of the light stabilizers and ultraviolet absorbers that can be used with these heat stabilizers include "Sumisorb" and "Irgafos" series of phosphite compounds.

The polylactic acid or polylactic acid copolymer produced according to the present invention has a markedly improved thermal fluidity of the polymer, facilitates the polymerization operation, especially mixing, degassing and feeding, and is a uniform and excellent polymer. Is obtained. Also, with respect to molding, since the heat fluidity is remarkably improved, good molded products and molding operability can be obtained.

The polymer of the present invention may optionally contain an antioxidant, an ultraviolet absorber, a lubricant, a pigment, a colorant, an antistatic agent,
A release agent and other well-known additives and fillers can be mixed and mixed.

Various polymerization apparatuses can be used for the polymerization of polylactic acid. However, since the polymerization takes place at least at the melting point or higher of the produced polymer, if the polymerization time becomes long, the progress of depolymerization rather causes a decrease in the degree of polymerization or coloring, as described above. Therefore, as a preferable polymerization apparatus,
Rather than a vertical stirring tank for uniform stirring, a twin-screw kneading extruder with a high plug flow property, a horizontal reactor used for polyester polymerization, or a device similar in stirring and feeding function. It is possible to obtain stable quality polylactic acid.

For example, a twin-screw kneading extruder (hereinafter abbreviated as a twin-screw kneader) is provided in parallel, and the shafts rotating in the same direction or in the opposite direction are engaged with each other by a screw (feed section) and a mesh 2 which are also meshed with each other. It is equipped with multiple (many) blades or 3-blade stirring elements, and the cylinder (cylindrical part) is supplied with raw materials and additives as necessary, degassed, and exhausted for reaction under reduced pressure. This is an apparatus provided with one or more vent holes for performing the above. With the twin-screw kneader, the polymerization raw material or the polymer during and after the polymerization is stirred, mixed and moved very effectively, and the reaction speed is considerably increased.

In addition to the above-mentioned kneader-type polymerization machine, a large number of disk-shaped or similar stirring elements are arranged on two rotating shafts so as to overlap each other, and their cross sections are circular, oval, and similar. A horizontal or vertical tank-shaped reaction vessel can also be used in the continuous polymerization of the present invention because it has little dead space, has a self-cleaning action, and can be depressurized.

In the polymerization of the present invention, a plurality of polymerization apparatuses such as the above-mentioned single-screw extruder, twin-screw kneader, and twin-screw stirring reactor may be used in a multi-stage combination, or by a vertical stirring tank. It is also possible to carry out the first-stage polymerization and then to add it to the above-mentioned horizontal type reaction tank.

The obtained polymer can be directly spun (direct spinning) or formed into a film (direct film formation) as it is, but can also be pelletized once, and then molded articles, films and fibers can be produced. Alternatively, once dissolved in a solvent, fibers can be produced by wet spinning or dry spinning, coating or impregnation of film, paper, non-woven fabric, etc.,
It can be emulsified to form fine particles. Particularly in melt spinning, since the polylactic acid of the present invention has good moldability, partially oriented yarn (POY) produced by high-speed spinning at a spinning speed of 3000 m / min or higher oriented yarn (HOY) at a spinning speed of 4000 m / min or more is used. ) And a spin draw method (SPD) in which spinning and drawing are continuously performed, and a spunbonded nonwoven fabric in which spinning and non-woven are performed simultaneously or continuously are also excellent in process adaptability.

[0035]

EFFECT OF THE INVENTION The polymer obtained by the present invention is superior in heating stability and temporal stability of a molded product as compared with conventional polymers. In addition, it has significantly improved melt flowability compared to conventional homopolymers, and can be applied to spunbonded nonwoven fabrics, various containers, injection molded products of various parts, films and sheets, as well as the production of continuous long fibers and short fibers. It is possible. or,
Stable operability and quality can be obtained even in long-term polymerization. Since the polymer of the present invention has a melting point of 110 ° C. or higher, it has features that it can be applied to a great number of applications and there are few problems in the processing stage as compared with conventional biodegradable resins. For example, molded articles such as food containers are 100
It is necessary to be able to sterilize with boiling water at ℃,
Therefore, the melting point is 110 ° C or higher, preferably 130 ° C.
Although the above is required, the polymer of the present invention has sufficiently satisfactory performance. Similarly when applied to fibers, 100
Can withstand dyeing and sterilization at ℃.

In the present invention, the average molecular weight of polylactic acid and a copolymer containing it as a main component is determined by GPC (calibration with polystyrene standard sample) analysis of a 0.1% chloroform solution of the sample. Further, the melting point of the polymer is determined by measuring with a differential calorimetry (DSC) method (heating rate 10 ° C./min).

In the present invention, parts and% are parts by weight and% by weight unless otherwise specified. The solution viscosity (relative viscosity) of the polymer is 1 g of the sample, and phenol / tetrachloroethane =
It was dissolved in 100 ml of a mixed solvent of 6/4 (weight ratio) and measured at 20 ° C. with an Ubbelohde viscometer.

Impact strength is 1 / thickness with V-shaped notch
A test piece having a width of 2 inches and a width of 1/4 inch is measured by the Izod method (ASTM D-256a).

[0039]

The present invention will be described in more detail with reference to the following examples, but the invention is not limited thereto. Example 1 L-lactide having an optical purity of 99.8% that had been sufficiently dried (water content of 80 ppm or less) and had been previously melted was also melt-dried, and a hindered phenolic antioxidant Ciba Geigy Irganox 1010 was added to 0.1%. PEG with a number average molecular weight of 4000 (NOF # 4000) added with 1%
And are supplied to the raw material supply section of the twin-screw kneader at a ratio of 98/2. At the same time, as a polymerization catalyst, 0.3 against lactide
% Tin dioctylate is added. The twin-screw kneader has a diameter of 2
A feed screw of 5 mm and a stirring element having a thickness of 7 mm and two blades are combined, and a feed screw is attached to the raw material supply section and the two vent holes, and a stirring element is attached to the other portions. The cross section of the cylinder has an oval shape with a constricted central portion, the temperature is 190 ° C., and nitrogen gas is supplied from the first vent hole and exhausted from the second vent hole. The two rotating shafts rotate in the same direction, and the rotation speed is 40 times / min. The polymer discharged from the kneader is sent under pressure by a gear pump, filtered through a 20 μm filter, and has a diameter of 3 m.
Approximately 3 mm after being extruded from the m nozzle and cooled with water and solidified
To obtain chips. The average residence (reaction) time of the polymer in the twin-screw kneader is 15 minutes. The chips were slightly yellowish but had excellent transparency.

The molecular weight of the obtained polylactic acid is 130,000.
The residual monomer (Mw <1000) was about 11%. The chip was treated with an acetone solvent containing 5% hydrochloric acid added at 7%, and the lactic acid monomer and the residual catalyst were each adjusted to 0.8.
%, 0.01% is used as a molding chip.

A predetermined amount of the heat stabilizer shown in Table 1 was added to and mixed with the chip, melted at 245 ° C. with an extruder having a single screw of 35 mm, and then a metering pump (gear pump).
A fixed amount of molten polymer is sent through the
It was spun from a spinneret having 25 holes, cooled in air, and oiled to obtain a wound semi-drawn yarn at a speed of 3000 m / min. Next, this semi-drawn yarn was drawn at a drawing temperature of 70 ° C. and a draw ratio of 1.7 times, heat-treated at 150 ° C. under tension, and wound at a speed of 800 m / min to obtain a drawn yarn of 75 denier / 25 filaments. Table 1 shows spinning and drawing operability and yarn characteristics.

[0042]

[Table 1]

Example 2 0.3% of each of the heat stabilizers shown in Table 2 was added to the chip of Example 1.
Using the same, spinning and drawing were performed in the same manner as in Example 1. The results are shown in Table 2. In all cases, thermal decomposition of polylactic acid during spinning was small, and good spinning operability and yarn quality could be obtained.

[0044]

[Table 2]

   ─────────────────────────────────────────────────── ─── Continued front page    (72) Inventor Eiichi Ozeki             1st Nishinokyo Kuwabara-cho, Nakagyo-ku, Kyoto City Stock Association             Shimadzu Corporation Sanjo Factory F-term (reference) 4J002 CF181 EJ016 EN056 EV066                       EW066 FD066                 4J029 AA02 AA05 AB04 AD01 AD10                       BA03 BA08 EA05 KH05                 4J200 AA10 BA05 BA14 CA01 CA06                       CA08 EA04

Claims (5)

[Claims] 1. A polylactic acid containing lactic acid as a main component is washed with a solvent that dissolves a lactic acid monomer, a cyclic dimer and a polymerization catalyst, and the residual monomer amount in the polymer is at most 1%.
A method for producing a polylactic acid resin, characterized in that the residual catalyst amount is at most 0.01%, and a heat stabilizer is added at least 0.05% at the time of molding. 2. The polylactic acid is a polylactic acid comprising at least 85% by weight of a lactic acid component and at most 15% by weight of polyethylene glycol, polypropylene glycol, or a polyethylene / propylene glycol polyalkylene glycol component. The method according to item 1. 3. The optical purity of the lactic acid component is at least 80%.
The method according to claim 1, wherein 4. A polylactic acid having a number average molecular weight of at least 8
The method according to claim 1, wherein the method is 0000. 5. The heat stabilizer is a hindered phenol type,
The method according to claim 1, which is an arylamine-based, phosphorus-based, or sulfur-based heat stabilizer.