KR20230133212A - Biodegradable film - Google Patents

Abstract

In the present invention, a biodegradable film comprising a hydroxyalkanoate-lactide copolymer and polybutylene adipate terephthalate (PBAT) is provided. According to the present invention, the biodegradable film having excellent tensile properties such as yield tensile strength and Young's modulus while maintaining environmental friendliness and biodegradability and containing bio raw materials can be provided.

Description

Biodegradable film {BIODEGRADABLE FILM}

The present invention relates to biodegradable films.

Recently, as interest in environmental protection and eco-friendliness has rapidly increased, the need for methods of growing eco-friendly agricultural products is increasing. Mulching is known as one of these eco-friendly farming methods. When growing crops, the surface of the soil is covered with a mulching film to prevent the growth of weeds, prevent pests and diseases, maintain soil moisture or regulate ground temperature, and in case of rain. This is a method to prevent soil erosion by rainwater and reduce pesticide use.

The mulching film used in this mulching farming method greatly contributes to the productivity of agricultural products, but there are difficulties in collecting and recycling after use. Usually, synthetic resins such as polypropylene and polyethylene are used and biodegradable ingredients are added as additives to provide biodegradability, but biodegradation of the synthetic resin itself is impossible. Additionally, synthetic resins left behind without being biodegraded have the problem of contaminating the soil.

Accordingly, there have been attempts to manufacture mulching films using polybutylene adipate terephthalate (PBAT), a biodegradable plastic. However, while polybutylene adipate terephthalate (PBAT) has high elongation, mechanical properties such as Young's modulus have been There are fewer problems compared to films such as polyethylene. In addition, polybutylene adipate terephthalate (PBAT) is a 100% petroleum-based material, so it has a low bio-material content.

Accordingly, attempts have been made to improve the physical properties and increase the content of bio-based materials by compounding various biodegradable materials with polybutylene adipate terephthalate (PBAT), but there is a difference between polybutylene adipate terephthalate and other biodegradable materials. There is a problem with low tensile properties due to low compatibility.

The present invention is intended to provide a biodegradable film with excellent tensile properties such as yield tensile strength and Young's modulus and an increased content of bio raw materials.

According to one embodiment of the present invention, a biodegradable film comprising a hydroxyalkanoate-lactide copolymer and polybutylene adipate terephthalate (PBAT) is provided.

Hereinafter, the biodegradable film according to specific embodiments of the invention will be described in more detail.

Throughout this specification, unless otherwise specified, “include” or “contains” refers to the inclusion of a certain component (or component) without particular limitation, excluding the addition of other components (or components). cannot be interpreted as

Throughout this specification, “polylactic acid prepolymer” refers to polylactic acid with a weight average molecular weight of 1,000 to 50,000 g/mol, which is obtained by oligomerizing lactic acid.

Throughout this specification, “poly(3-hydroxypropionate) prepolymer” refers to poly(3-hydroxypropionate) with a weight average molecular weight of 1,000 to 50,000 g/mol obtained by oligomerizing 3-hydroxypropionate. it means.

In addition, unless otherwise stated herein, the weight average molecular weight of polylactic acid prepolymer, poly(3-hydroxypropionate) prepolymer, and copolymer can be measured using gel permeation chromatography (GPC). . Specifically, the prepolymer or copolymer is dissolved in chloroform to a concentration of 2 mg/ml, then 20 μl is injected into GPC, and GPC analysis is performed at 40°C. At this time, the mobile phase of GPC uses chloroform and flows at a flow rate of 1.0 mL/min, the column uses two Agilent Mixed-Bs connected in series, and the detector uses an RI Detector. The Mw value is derived using a calibration curve formed using a polystyrene standard specimen. The weight average molecular weights of the polystyrene standard specimens were 2,000 g/mol, 10,000 g/mol, 30,000 g/mol, 70,000 g/mol, 200,000 g/mol, 700,000 g/mol, 2,000,000 g/mol, 4,000,000 g/mol, and 10,000,000. Nine types of g/mol were used.

Additionally, in this specification, the term “substituted or unsubstituted” refers to deuterium; halogen group; Nitrile group; nitro group; hydroxyl group; carbonyl group; ester group; imide group; amino group; Phosphine oxide group; Alkoxy group; Aryloxy group; Alkylthioxy group; Arylthioxy group; Alkyl sulphoxy group; Aryl sulfoxy group; silyl group; boron group; Alkyl group; Cycloalkyl group; alkenyl group; Aryl group; Aralkyl group; Aralkenyl group; Alkylaryl group; Alkylamine group; Aralkylamine group; heteroarylamine group; Arylamine group; Arylphosphine group; or substituted or unsubstituted with one or more substituents selected from the group consisting of heterocyclic groups containing one or more of N, O and S atoms, or substituted or unsubstituted with two or more of the above-exemplified substituents linked. . For example, “a substituent group in which two or more substituents are connected” may be a biphenyl group. That is, the biphenyl group may be an aryl group, or it may be interpreted as a substituent in which two phenyl groups are connected.

Conventionally, to produce a biodegradable film, only polybutylene adipate terephthalate was used, or polybutylene adipate terephthalate was compounded with other biodegradable materials, but the method using only polybutylene adipate terephthalate In this case, there is a problem in that mechanical properties such as Young's modulus are low and the content of bio raw materials is also low, and in the case of compounding polybutylene adipate terephthalate with other biodegradable materials, there is a problem in that tensile properties are low due to low compatibility between materials.

In response to this, the present inventors found that, in the case of a biodegradable film manufactured by compounding polybutylene adipate terephthalate (PBAT) with a hydroxyalkanoate-lactide copolymer, compatibility between materials was excellent, resulting in high yield tensile strength. The present invention was completed by finding that the tensile properties such as and Young's modulus were also excellent.

In addition, since the hydroxyalkanoate-lactide copolymer contains a large amount of bio raw materials and exhibits eco-friendly and biodegradable characteristics, the biodegradable film containing it also contains a large amount of bio raw materials while maintaining eco-friendly and biodegradable characteristics. It can be included.

According to one embodiment of the invention, a biodegradable film comprising a hydroxyalkanoate-lactide copolymer and polybutylene adipate terephthalate (PBAT) is provided.

The hydroxyalkanoate-lactide copolymer included in the biodegradable film according to the above embodiment is a block copolymer containing one or more polyhydroxyalkanoate (PHA; polyhydrxyalkanoate) blocks and one or more polylactic acid blocks. It may be a combination. As the hydroxyalkanoate-lactide copolymer contains the above-mentioned blocks, it can exhibit the environmental friendliness and biodegradability of polyhydroxyalkanoate and polylactic acid.

The hydroxyalkanoates include 3-hydroxybutyrate, 4-hydroxybutyrate, 2-hydroxypropionate, 3-hydroxypropionate, and (D)-3- having a medium chain length of 6 to 14 carbon atoms. It may be hydroxycarboxylate, 3-hydroxyvalate, 4-hydroxyvalate or 5-hydroxyvalate. Therefore, the hydroxyalkanoate-lactide copolymer is 3-hydroxybutyrate-lactide copolymer, 4-hydroxybutyrate-lactide copolymer, 2-hydroxypropionate-lactide copolymer, 3- It may be a hydroxypropionate-lactide copolymer, a 4-hydroxyvalate-lactide copolymer, or a 5-hydroxyvalate-lactide copolymer, for example, the hydroxyalkanoate-lactide. The copolymer may be a 3-hydroxypropionate-lactide copolymer to improve flexibility and mechanical properties.

The 3-hydroxypropionate-lactide copolymer may be a block copolymer obtained by polymerizing polylactic acid prepolymer and poly(3-hydroxypropionate) prepolymer.

The 3-hydroxypropionate-lactide copolymer exhibits the excellent tensile strength and elastic modulus characteristics of the polylactic acid prepolymer, while the poly(3-hydroxypropionate) prepolymer has a glass transition temperature (Tg). By increasing flexibility by lowering and improving mechanical properties such as impact strength, it is possible to prevent the brittleness of polylactic acid due to its poor elongation.

The polylactic acid prepolymer may be manufactured by fermentation or polycondensation of lactic acid.

The polylactic acid prepolymer may have a weight average molecular weight of 1,000 g/mol or more, or 5,000 g/mol or more, or 6,000 g/mol or more, or 8,000 g/mol or more, and 50,000 g/mol or less, or 30,000 g/mol or less, When it is desired to increase the crystallinity of the block containing repeating units derived from polylactic acid prepolymer in the final manufactured block copolymer, the polylactic acid prepolymer must be greater than 20,000 g/mol, or 22,000 g/mol or more, or 23,000 g/mol. It is preferable to have a high weight average molecular weight of more than or equal to 25,000 g/mol, and less than or equal to 50,000 g/mol, or less than or equal to 30,000 g/mol, or less than or equal to 28,000 g/mol, or less than or equal to 26,000 g/mol.

If the weight average molecular weight of the polylactic acid prepolymer is less than 20,000 g/mol, the polymer crystals are small and it is difficult to maintain the crystallinity of the polymer in the final manufactured block copolymer. If the weight average molecular weight of the polylactic acid prepolymer exceeds 50,000 g/mol, it is difficult to maintain the crystallinity of the polymer. During polymerization, the side reaction rate occurring within the prepolymer chain becomes faster than the reaction rate between polylactic acid prepolymers.

Meanwhile, 'lactic acid' used in the present invention refers to L-lactic acid, D-lactic acid, or a mixture thereof.

The poly(3-hydroxypropionate) prepolymer may be manufactured by fermenting or condensation polymerization of 3-hydroxypropionate.

The weight average molecular weight of the poly(3-hydroxypropionate) prepolymer is 1,000 g/mol or more, or 5,000 g/mol or more, or 8,000 g/mol or more, or 8,500 g/mol or more, and 50,000 g/mol or less, Alternatively, it may be 30,000 g/mol or less, and when it is desired to increase the crystallinity of the repeating unit derived from the poly(3-hydroxypropionate) prepolymer in the final manufactured block copolymer, the poly(3-hydroxypropionate) The prepolymer has a high weight average molecular weight of more than 20,000 g/mol, or more than 22,000 g/mol, or more than 25,000 g/mol, and less than or equal to 50,000 g/mol, or less than or equal to 30,000 g/mol, or less than or equal to 28,000 g/mol. desirable.

As explained in the polylactic acid prepolymer, if the weight average molecular weight of the poly(3-hydroxypropionate) prepolymer is 20,000 g/mol or less, the polymer crystals are small, making it difficult to maintain the crystallinity of the polymer in the final manufactured block copolymer. It is difficult, and if the weight average molecular weight of the poly(3-hydroxypropionate) prepolymer exceeds 50,000 g/mol, the side reaction rate occurring inside the prepolymer chain is higher than the reaction rate between poly(3-hydroxypropionate) prepolymers during polymerization. becomes faster.

That is, at least one of the polylactic acid prepolymer and the poly(3-hydroxypropionate) prepolymer may have a weight average molecular weight of more than 20,000 g/mol and less than or equal to 50,000 g/mol.

Meanwhile, the lactic acid and 3-hydroxypropionate may be plastic and biodegradable compounds produced from renewable sources by microbial fermentation, and polylactic acid prepolymer and poly(3-hydroxypropionate) formed by polymerizing them The block copolymer containing the prepolymer may also exhibit environmental friendliness and biodegradability. For this reason, the biodegradable film containing the block copolymer can contain a large amount of bio raw materials while exhibiting environmental friendliness and biodegradability.

The 3-hydroxypropionate-lactide copolymer is a block copolymer in which polylactic acid prepolymer and poly(3-hydroxypropionate) prepolymer are polymerized, and in the block copolymer, the polylactic acid prepolymer and poly(3 -Hydroxypropionate) The weight ratio of the prepolymer is 95:5 to 50:50, 90:10 to 55:45, 90:10 to 60:40, 90:10 to 70:30, or 90:10 to 80:20. It can be. If too little of the poly(3-hydroxypropionate) prepolymer is included in the polylactic acid prepolymer, brittleness may increase, and the poly(3-hydroxypropionate) prepolymer may increase brittleness. If too much prepolymer is included, the molecular weight may be lowered and processability and heat stability may be reduced.

As described above, the 3-hydroxypropionate-lactide copolymer includes one or more poly(3-hydroxypropionate) blocks and one or more polylactic acid blocks, and exhibits high crystallinity. You can.

For example, the 3-hydroxypropionate-lactide copolymer has a poly in the copolymer calculated according to the following equations 1 and 2 using the crystallization temperature and melting temperature measured through differential scanning calorimetry. The crystallinity of the lactic acid block ( _{Xc_PLA} ) may be greater than 0 and 50 or less, or the crystallinity of the poly(3-hydroxypropionate) block ( _{Xc_P(3HP)} ) may be 0 to 50, or greater than 0 and 50 or less.

In addition, the total sum of the crystallinity degree of the polylactic acid block and the crystallinity degree of the poly(3-hydroxypropionate) block in the copolymer is 20 to 100, more specifically, 20 or more, or 30 or more, or 32 or more, It may be 100 or less, or 70 or less, or 50 or less, or 48 or less.

As the copolymer satisfies the above-mentioned degree of crystallinity, flexibility and mechanical properties can be well balanced and improved, and it can simultaneously exhibit the excellent strength characteristics of polylactic acid and the excellent elongation characteristics of poly(3-hydroxypropionate).

On the other hand, if the total crystallinity degree is too high, biodegradability and processability may be reduced, and if the total crystallinity degree is too low, the strength may be reduced.

[Equation 1]

Crystallinity of polylactic acid block ( _{Xc_PLA} )= [(PLA Tm area)-(PLA Tcc area)]/93.7

In Equation 1, the PLA Tm area is the integral value of the peak at the melting temperature (Tm) of the polylactic acid (PLA) block in the block copolymer measured through differential scanning calorimetry, and the PLA Tcc area is the differential scanning area. It may be the integral value of the peak at the crystallization temperature (Tcc) of the polylactic acid block in the block copolymer measured through calorimetric analysis.

[Equation 2]

Crystallinity of poly(3-hydroxypropionate) block (Xc_ _P(3HP) )= [(P(3HP) Tm area)-(P(3HP) Tcc area)]/64

In Equation 2, the P(3HP) Tm area is the melting temperature (Tm) of the poly(3-hydroxypropionate) (P(3HP)) block in the block copolymer measured through differential scanning calorimetry. is the integral value for the peak, and the P(3HP) Tcc area is the integral for the peak at the crystallization temperature (Tcc) of the poly(3-hydroxypropionate) block in the block copolymer measured through differential scanning calorimetry. It can be a value.

In addition, the integrated value for the peaks at Tm and Tcc means a value obtained by integrating the lower areas of the peaks representing Tm and Tcc, respectively.

At this time, differential scanning calorimetry for measuring Tm and Tcc of each block can be performed using PerkinElmer DSC800 equipment. In addition, the sample to be analyzed was heated at a rate of 10°C per minute from 25°C to 250°C under a nitrogen atmosphere, cooled again from 250°C to -50°C at a rate of -10°C per minute, and then again from -50°C to 250°C. By increasing the temperature at a rate of 10°C per minute and obtaining an endothermic curve, Tm and Tcc can be confirmed.

The hydroxyalkanoate-lactide copolymer has a weight average molecular weight (Mw) measured using gel permeation chromatography (GPC) of 50,000 to 300,000 g/mol, and more specifically, 50,000 g/mol. mol or more, 70,000 g/mol or more, or 100,000 g/mol or more, and has a weight average molecular weight of 300,000 g/mol or less, or 200,000 g/mol or less, or 150,000 g/mol or less. If the weight average molecular weight of the hydroxyalkanoate-lactide copolymer is too small, the overall mechanical properties may be significantly reduced, and if the weight average molecular weight is too large, the process may be difficult and processability and elongation may be low.

The biodegradable film according to the embodiment includes the hydroxyalkanoate-lactide copolymer, for example, may be included in 3 to 40% by weight based on the total 100% by weight of the biodegradable film, and more specifically, It may be included in an amount of 3% by weight or more, 5% by weight or more, 7% by weight or less, or 40% by weight or less, 35% by weight or less, and 30% by weight or less.

If the hydroxyalkanoate-lactide copolymer is included in too little of the biodegradable film, tensile properties such as Young's modulus and yield tensile strength may decrease, and the hydroxyalkanoate-lactide copolymer may be biodegradable. If too much is included in the film, the elongation may be lowered.

The biodegradable film according to the above embodiment includes polybutylene adipate terephthalate (PBAT).

The polybutylene adipate terephthalate (PBAT) is a biodegradable resin and may be included in an amount of 30 to 98% by weight based on the total 100% by weight of the biodegradable film, and more specifically, 30% by weight or more, 40% by weight or more, or 50% by weight. % or more, or may be included in 98 wt% or less, 95 wt% or less, or 92 wt% or less.

If too little polybutylene adipate terephthalate (PBAT) is included in the biodegradable film, the elongation may be lowered, and if too much polybutylene adipate terephthalate (PBAT) is included in the biodegradable film, the Young's modulus and Tensile properties such as yield tensile strength may decrease.

The weight ratio of the hydroxyalkanoate-lactide copolymer and polybutylene adipate terephthalate (PBAT) included in the biodegradable film according to the embodiment is 5:95 to 50:50, 5:95 to 40. :60, 10:90 to 30:70.

If too little polybutylene adipate terephthalate (PBAT) is included compared to the hydroxyalkanoate-lactide copolymer, the elongation may be lowered, and compared to the hydroxyalkanoate-lactide copolymer, the polybutylene adipate terephthalate (PBAT) may be lowered. If too much butylene adipate terephthalate (PBAT) is included, tensile properties such as Young's modulus and yield tensile strength may be reduced.

The biodegradable film according to the above embodiment may further include thermoplastic starch.

The present inventors found that, in the case of a biodegradable film produced by compounding polybutylene adipate terephthalate (PBAT) with a hydroxyalkanoate-lactide copolymer and thermoplastic starch, the yield tensile strength was excellent due to excellent compatibility between materials. It was found that tensile properties such as strength and Young's modulus were also excellent.

In addition, the biodegradable film is used to increase the processability of polybutylene adipate terephthalate and to speed up the biodegradation rate. It may further contain thermoplastic starch.

The thermoplastic starch may be a starch in which a plasticizer is added to starch, a natural polymer, to provide thermoplasticity that allows the shape to be freely changed without being carbonized above a certain temperature, like existing general-purpose resins such as polyethylene, polystyrene, and polypropylene.

The thermoplastic starch may include one or more selected from the group consisting of rice starch, wheat starch, corn starch, sweet potato starch, potato starch, tapioca starch, cassava starch, and modified starches thereof.

Additionally, the plasticizer included in starch, a natural polymer, may be one or more selected from the group consisting of isosorbide, glycerol, sorbitol, fructose, formamide, xylitol, corn oil, and edible oil.

The plasticizer may be included in an amount of 5% to 50% by weight, 10% to 45% by weight, or 15% to 35% by weight based on the total 100% by weight of the thermoplastic starch.

The thermoplastic starch may be included in an amount of 10 to 70% by weight based on the total 100% by weight of the biodegradable film, and more specifically, 10% by weight or more, 15% by weight or more, 20% by weight or more, or 70% by weight or less, 60% by weight. Hereinafter, it may be included in an amount of 50% by weight or less.

If the thermoplastic starch is included in too little of the biodegradable film, the biodegradation rate may be slowed and tensile properties such as Young's modulus and yield tensile strength may be lowered, and if the thermoplastic starch is included in too much of the biodegradable film, the elongation may be lowered. there is.

As described above, hydroxyalkanoate-lactide copolymer, polybutylene adipate terephthalate (PBAT), and thermoplastic starch are added to the biodegradable film, and the hydroxyalkanoate-lactide copolymer and The thermoplastic starch may be included in an amount of 10 to 100 parts by weight, 20 to 90 parts by weight, 30 to 80 parts by weight, or 30 to 70 parts by weight based on a total of 100 parts by weight of polybutylene adipate terephthalate (PBAT).

The biodegradable film according to the embodiment may further include a compatibilizer to improve mechanical properties by improving the bonding strength of the hydroxyalkanoate-lactide copolymer and polybutylene adipate terephthalate (PBAT). there is. In addition, the compatibilizer can improve mechanical properties by improving the bonding strength of hydroxyalkanoate-lactide copolymer, polybutylene adipate terephthalate (PBAT), and thermoplastic starch. The compatibilizer can act as a chain extender to increase molecular weight, increase melt viscosity, and improve formability such as stretchability.

The compatibilizer is not limited thereto, but may be a compound containing at least one functional group selected from a glycidyl group, an acid anhydride group, a carbodiimide group, an isocyanate group, an oxazoline group, and an amino group.

Examples of compounds containing the glycidyl group include glycidyl ether compounds, glycidyl ester compounds, glycidylamine compounds, glycidyl imide compounds, glycidyl (meth)acrylate compounds, and alicyclic epoxy compounds. I can hear it. Commercially available products include DuPont's "BIOMAX" (registered trademark) Strong series, which is a copolymer of ethylene, acrylic acid ester, and glycidyl (meth)acrylate, and Arkema's "LOTADER" (registered trademark) series. , BASF's "JONCRYL" (registered trademark) series, which is an acrylic/styrene-based copolymer containing glycidyl groups, and Toa Kosei Co., Ltd.'s "Rezeda" (registered trademark) series, which is an acrylic resin containing glycidyl groups. 'Alphone' (registered trademark) series, etc. Additionally, examples of the compound containing the acid anhydride group include compounds containing succinic anhydride, maleic anhydride, phthalic anhydride, etc. Commercially available products include Arkema's registered patent 10-1970847 - 10 - "BONDINE" (registered trademark) series, which is a copolymer of ethylene, acrylic acid ester, and maleic anhydride, and Arkema's "OREVAC" (registered trademark), which is a maleic anhydride graft polymer. registered trademark) series, DuPont's "Bynel" series, Sanyo Kasei Kogyo Co., Ltd.'s "UMEX" (registered trademark) series, a polymer copolymerized with styrene-ethylene-butylene-styrene copolymer (SEBS) and maleic anhydride. and the "KRATON" (registered trademark) series from Kraton. The compound containing the carbodiimide group is a compound having at least one carbodiimide group represented by (-N=C=N-) in the molecule, and commercially available compounds include "Carbodiimide Group" from Nisshin Boseki Co., Ltd. Examples include the “Body Light” (registered trademark) series and the “STABAXOL” (registered trademark) series from Rhein Chemie. Examples of the compound containing the isocyanate group include hexamethylene diisocyanate.

For example, the compatibilizer may include a repeating unit represented by the following formula (1).

[Formula 1]

In Formula 1,

R ₁ to R ₆ are each independently hydrogen, deuterium, hydroxy, nitro, amino, substituted or unsubstituted alkyl having 2 to 60 carbon atoms, substituted or unsubstituted alkoxy having 2 to 60 carbon atoms, or substituted or unsubstituted 2 to 60 carbon atoms. Alkenyl of 60, substituted or unsubstituted cycloalkyl of 4 to 60 carbon atoms, substituted or unsubstituted aryl of 6 to 60 carbon atoms, or substituted or unsubstituted carbon atoms containing one or more of O, N, Si and S It may be 2 to 60 heteroaryl.

For example, R ₁ to R ₃ may each independently be hydrogen or deuterium.

Additionally, R ₄ and R ₆ may each independently be hydrogen, deuterium, methyl, ethyl, or propyl.

Additionally, R ₅ may be alkyl having 2 to 60 carbon atoms.

x, y, and z may each independently be integers from 1 to 20.

The compatibilizer may be included in an amount of 0.1 to 10 parts by weight based on 100 parts by weight of the biodegradable film, and more specifically, 0.1 parts by weight or more, 0.2 parts by weight or more, 0.3 parts by weight or more, 10 parts by weight or less, 5 parts by weight or less, It may contain less than 3 parts by weight.

If the compatibilizer is included in too little of the biodegradable film, the mechanical properties are not improved, and if the compatibilizer is included in too much of the biodegradable film, the melt viscosity may increase excessively and formability may be reduced.

The biodegradable film according to the above embodiment may have a yield tensile strength measured according to ASTM D882-07 of 7 MPa or more, 8 MPa or more, or 7 MPa to 30 MPa.

Additionally, the biodegradable film may have a Young's Modulus measured according to ASTM D882-07 of 80 MPa or more, 85 MPa or more, 90 MPa or more, and 100 MPa to 800 MPa.

The thickness of the biodegradable film according to the above embodiment may be 10 to 300 ㎛, more specifically, 10 ㎛ or more, 20 ㎛ or more, 30 ㎛ or more, or 300 ㎛ or less, 200 ㎛ or less, and 150 ㎛ or less. When the thickness of the film is within the above-mentioned range, elasticity can be strengthened, handling properties can be excellent, and the winding state and unwinding properties of the roll can be improved.

If the film thickness is too thin, the tensile strength, tear strength, and elongation may deteriorate, which may cause holes or tears in the film during use, and if the film thickness is too thick, unit price competitiveness may be reduced.

The biodegradable film can be used as agricultural mulching film, disposable gloves, individual medical packaging, food packaging, garbage bags, or bags for various industrial products.

The method of producing the biodegradable film is not particularly limited, but a melt-kneading method of melting and kneading hydroxyalkanoate-lactide copolymer, polybutylene adipate terephthalate (PBAT), and/or thermoplastic starch is used, or A composition can be prepared by uniformly mixing a solution in which each component is dissolved in a solvent and then removing the solvent.

In the case of the melt kneading method, there are no particular restrictions on the method, but conventional mixers such as a kneader, roll mill, Banbury mixer, single-screw or twin-screw extruder can be used. During melt kneading, the temperature of the extruder may be 150°C to 240°C, 160°C to 220°C, or 170°C to 200°C.

The biodegradable film can be obtained by conventional film production methods such as the known inflation method, tubular method, and T die casting method, using a composition prepared by a melt kneading method or the like. For example, the composition can be pelletized and the pellets dried at 60 to 100° C. for 6 hours or more to control the moisture content to 1,200 ppm or less, 500 ppm or less, or 200 ppm or less.

Thereafter, the pelletized composite can be applied to a release film, placed in a thermocompressor, and pressure applied to produce a film. At this time, the temperature may be 130°C to 250°C, 150°C to 220°C, or 160°C to 200°C, and the pressure may be 5 MPa to 20 MPa, 8 MPa to 17 MPa, or 10 MPa to 15 MPa.

According to the present invention, a biodegradable film containing bio raw materials and having excellent tensile properties such as yield tensile strength and Young's modulus while maintaining environmental friendliness and biodegradability can be provided.

1 is a stress-strain curve for the films prepared in Examples 1 to 4 and Comparative Example 1.
Figure 2 is a stress-strain curve for the films prepared in Examples 5 to 9 and Comparative Example 2.

The invention is explained in more detail in the following examples. However, the following examples only illustrate the present invention, and the content of the present invention is not limited by the following examples.

Preparation Example 1: Preparation of 3-hydroxypropionate-lactide block copolymer

(1) Production of polylactic acid prepolymer

25 g of 85% L-lactic acid aqueous solution was added to a 100 ml Schlenk flask in an oil bath and the pressure was reduced for 2 hours at 70°C and 50 mbar to remove moisture in L-lactic acid. Afterwards, based on 100 parts by weight of lactate, 0.4 parts by weight of p-toluenesulfonic acid (p-TSA) and SnCl ₂ catalyst Add 0.1 part by weight of each and simmer at a temperature of 150°C for 12 hours. During the melt condensation polymerization reaction. After the reaction was completed, the reactant was dissolved in chloroform and extracted with methanol to obtain a polylactic acid prepolymer (weight average molecular weight: 8,000 g/mol).

(2) Poly(3-hydroxypropionate) prepolymer production

Add 25 ml of 60% 3-hydroxypropionate aqueous solution to a 100 ml Schlenk flask in an oil bath, remove moisture in the 3-hydroxypropionate for 3 hours at 50 ℃ and 50 mbar, and then incubate at 70 ℃ and After oligomerization at 20 mbar for 2 hours, p-toluenesulfonic acid (p-TSA) catalyst based on 100 parts by weight of 3-hydroxypropionate was added to the reaction flask. Add 0.4 parts by weight and simmer for 24 hours at a temperature of 110°C. During the melt condensation polymerization reaction. After the reaction was completed, the reactant was dissolved in chloroform and extracted with methanol to obtain poly(3-hydroxypropionate) prepolymer (weight average molecular weight: 26,000 g/mol).

(3) Preparation of block copolymers

The polylactic acid prepolymer and the poly(3-hydroxypropionate) prepolymer were mixed in a 100 ml Schlenk flask in an oil bath at a weight ratio of 9:1, added to a total content of 30 g, and p-toluenesulfonic acid ( 90 mg of p-TSA) was added, and annealing was performed at 60°C for 3 hours. Afterwards, using an evaporator, mix at 150°C and 0.5 mbar for 24 hours and perform solid phase polymerization to produce 3-hydroxypropionate-lactide. A block copolymer (weight average molecular weight: 130,000 g/mol) was prepared.

Meanwhile, the weight average molecular weight of the polylactic acid prepolymer, poly(3-hydroxypropionate) prepolymer, and block copolymer was measured using gel permeation chromatography (GPC).

Preparation Example 2: Preparation of thermoplastic starch

Based on dry weight, 225 g of corn starch and 75 g of glycerol were mixed in a mixer and then put into an extruder for compounding. The temperature range of the extruder was 80 to 150 °C, the screw speed was set to 150 rpm, and the extruded strand was cut with a pelletizer to prepare thermoplastic starch pellets.

<Examples and Comparative Examples>

Example 1: Preparation of biodegradable film

After hand mixing 90 g of polybutylene adipate terephthalate (PBAT, Solpol 1000N, SOLTECH) and 10 g of 3-hydroxypropionate-lactide block copolymer prepared in Preparation Example 1 based on dry weight. It was put into an extruder and compounded. The temperature range of the extruder was 170 to 190 °C, the screw speed was set to 150 rpm, and the extruded strand was cut with a pelletizer to prepare composite pellets. After applying the prepared composite pellet to the release film, it was placed in a thermocompressor and a pressure of 12 MPa was applied at 190° C. to prepare a film with a thickness of 100 μm.

Examples 2 to 5 and Comparative Example 1: Production of biodegradable film

The same as Example 1 except that the contents of polybutylene adipate terephthalate, 3-hydroxypropionate-lactide block copolymer, and compatibilizer (Joncryl ^® ADR 4468, BASF) were used as shown in Table 1 below. The film was manufactured using this method. Meanwhile, in Table 1 above, “-“ means absent.

(Unit: g) Polybutylene adipate terephthalate 3-Hydroxypropionate-lactide block copolymer compatibilizer Example 1 90 10 - Example 2 80 20 - Example 3 90 10 One Example 4 80 20 One Comparative Example 1 100 - -

Example 5: Manufacturing biodegradable film

Based on dry weight, 42 g of polybutylene adipate terephthalate (PBAT, Solpol 1000N, SOLTECH), 18 g of 3-hydroxypropionate-lactide block copolymer prepared in Preparation Example 1, and Preparation Example 2 40 g of thermoplastic starch manufactured in and 0.5 g of compatibilizer (Joncryl ^® ADR 4468, BASF) were mixed by hand and then put into an extruder for compounding. The temperature range of the extruder was 170 to 190 °C, the screw speed was set to 150 rpm, and the extruded strand was cut with a pelletizer to prepare composite pellets. After applying the prepared composite pellet to the release film, it was placed in a thermocompressor and a pressure of 12 MPa was applied at 160° C. to prepare a film with a thickness of 100 μm.

Examples 6 to 9 and Comparative Example 2: Preparation of biodegradable film

A film was prepared in the same manner as in Example 5, except that the contents of polybutylene adipate terephthalate, 3-hydroxypropionate-lactide block copolymer, thermoplastic starch, and compatibilizer were used as shown in Table 2 below. . Meanwhile, in Table 2 above, “-“ means absent.

Comparative Example 3: Production of biodegradable film

Based on dry weight, 90 g of polybutylene adipate terephthalate (PBAT, Solpol 1000N, SOLTECH) and 10 g of polylactic acid (PLA, product name: PLA 2003D, NATUREWORKS) are mixed by hand and then put into an extruder for compounding. did. The temperature range of the extruder was 170 to 190 °C, the screw speed was set to 150 rpm, and the extruded strand was cut with a pelletizer to prepare composite pellets. After applying the prepared composite pellet to the release film, it was placed in a thermocompressor and a pressure of 12 MPa was applied at 190° C. to prepare a film with a thickness of 100 μm.

(Unit: g) Polybutylene adipate terephthalate 3-Hydroxypropionate-lactide block copolymer thermoplastic starch compatibilizer Example 5 42.0 18.0 40.0 0.5 Example 6 48.0 12.0 40.0 0.5 Example 7 52.5 22.5 25.0 0.5 Example 8 60.0 15.0 25.0 0.8 Example 9 67.5 7.5 25.0 1.0 Comparative Example 2 100 - - - Comparative Example 3 90 polylactic acid 10 - -

evaluation

1. Tensile property evaluation

The tensile properties of the films of Examples and Comparative Examples were evaluated according to ASTM D882-07. Tensile properties include tensile strength at yield, Young's modulus, ultimate tensile strength, and elongation at break, and the results are shown in Tables 3 and 4 below.

Yield tensile strength is the maximum stress at which permanent inelastic deformation begins. The yield point is the point (load) at which the material yields, i.e. an increase in strain occurs without an increase in stress. Young's modulus is the ratio of stress to strain within the elastic region of the stress-strain curve (before the yield point). Ultimate tensile strength is the maximum stress that a material can withstand before breaking. Elongation at break is the strain at break, or the rate of change in length at break.

Figure 1 is a stress-strain curve showing the tensile property evaluation results of Examples 1 to 4 and Comparative Example 1, and Figure 2 is a stress-strain curve showing the tensile property evaluation results of Examples 5 to 9 and Comparative Example 2. It is a stress-strain curve, and Young's modulus was calculated as the highest slope value in the initial part of the curve, and the yield tensile strength is the tensile strength at the point where the Young's modulus and slope begin to differ by more than 3%.

Yield tensile strength (MPa) Young's modulus (MPa) Maximum tensile strength (MPa) Elongation at break (%) Example 1 7.80 98 22.8 629 Example 2 8.93 133 16.8 552 Example 3 7.90 86 25.5 603 Example 4 8.27 96 26.6 599 Comparative Example 1 6.85 79 40.0 831

According to Table 3, it was confirmed that Examples 1 to 4 were excellent in tensile properties including yield tensile strength, Young's modulus, ultimate tensile strength, and elongation at break, and in particular, the yield tensile strength and Young's modulus were significantly superior. In addition, Examples 3 and 4, which further included a compatibilizer, confirmed that the maximum tensile strength and elongation at break were superior to those without a compatibilizer. On the other hand, it was confirmed that Comparative Example 1 using only polybutylene adipate terephthalate was inferior in yield tensile strength and Young's modulus.

Yield tensile strength (MPa) Young's modulus (MPa) Maximum tensile strength (MPa) Elongation at break (%) Example 5 10.8 347 10.8 20 Example 6 9.1 238 9.4 66 Example 7 8.9 276 10.1 116 Example 8 8.4 182 12.2 338 Example 9 7.4 147 17.4 607 Comparative Example 2 6.9 79 40.0 831 Comparative Example 3 - 79 26.1 756

According to Table 4, it was confirmed that Examples 5 to 9 were excellent in tensile properties including yield tensile strength, Young's modulus, maximum tensile strength, and elongation at break, and in particular, were significantly superior in yield tensile strength and Young's modulus. Meanwhile, it was confirmed that Comparative Example 2 using only polybutylene adipate terephthalate was inferior in yield tensile strength and Young's modulus, and Comparative Example 3 using polylactic acid was inferior in Young's modulus.

Claims (16)

Containing hydroxyalkanoate-lactide copolymer and polybutylene adipate terephthalate (PBAT),
Biodegradable film.
According to paragraph 1,
further comprising thermoplastic starch,
Biodegradable film.
According to paragraph 2,
The thermoplastic starch includes one or more selected from the group consisting of rice starch, wheat starch, corn starch, sweet potato starch, potato starch, tapioca starch, cassava starch, and modified starches thereof.
Biodegradable film.
According to paragraph 1,
The hydroxyalkanoate-lactide copolymer is a 3-hydroxypropionate-lactide copolymer,
Biodegradable film.
According to paragraph 4,
The 3-hydroxypropionate-lactide copolymer is a block copolymer in which polylactic acid prepolymer and poly(3-hydroxypropionate) prepolymer are polymerized.
Biodegradable film.
According to clause 5,
At least one of the polylactic acid prepolymer and poly(3-hydroxypropionate) prepolymer has a weight average molecular weight of more than 20,000 g/mol and less than or equal to 50,000 g/mol,
Biodegradable film.
According to clause 5,
The weight ratio of the polylactic acid prepolymer and poly(3-hydroxypropionate) prepolymer is 95:5 to 50:50,
Biodegradable film.
According to clause 5,
The 3-hydroxypropionate-lactide copolymer has a total sum of the crystallinity degree of the polylactic acid block and the crystallinity degree of the poly(3-hydroxypropionate) block, calculated according to Equations 1 and 2 below, of 20 to 100. person,
Biodegradable Film:
[Equation 1]
Crystallinity of polylactic acid block ( _{Xc_PLA} )= [(PLA Tm area)-(PLA Tcc area)]/93.7
(In Equation 1 above, the PLA Tm area is the integral value of the peak at the melting temperature (Tm) of the polylactic acid (PLA) block in the block copolymer measured through differential scanning calorimetry, and the PLA Tcc area is the differential This is the integrated value of the peak at the crystallization temperature (Tcc) of the polylactic acid block in the block copolymer measured through scanning calorimetry.)
[Equation 2]
Crystallinity of poly(3-hydroxypropionate) block (Xc_ _P(3HP) )= [(P(3HP) Tm area)-(P(3HP) Tcc area)]/64
(In Equation 2 above, the P(3HP) Tm area is the melting temperature (Tm) of the poly(3-hydroxypropionate) (P(3HP)) block in the block copolymer measured through differential scanning calorimetry. is the integral value for the peak at, and the P(3HP) Tcc area is for the peak at the crystallization temperature (Tcc) of the poly(3-hydroxypropionate) block in the block copolymer measured through differential scanning calorimetry. (integral value)
According to paragraph 1,
The hydroxyalkanoate-lactide copolymer has a weight average molecular weight of 50,000 to 300,000,
Biodegradable film.
According to paragraph 1,
The weight ratio of the hydroxyalkanoate-lactide copolymer and polybutylene adipate terephthalate (PBAT) is 5:95 to 50:50,
Biodegradable film.
According to paragraph 2,
Containing 10 to 100 parts by weight of the thermoplastic starch based on a total of 100 parts by weight of the hydroxyalkanoate-lactide copolymer and polybutylene adipate terephthalate (PBAT),
Biodegradable film.
According to paragraph 1,
The biodegradable film further contains a compatibilizer,
Biodegradable film.
According to clause 12,
The compatibilizer contains a repeating unit represented by the following formula (1),
Biodegradable Film:
[Formula 1]

In Formula 1,
R ₁ to R ₆ are each independently hydrogen, deuterium, hydroxy, nitro, amino, substituted or unsubstituted alkyl having 2 to 60 carbon atoms, substituted or unsubstituted alkoxy having 2 to 60 carbon atoms, or substituted or unsubstituted 2 to 60 carbon atoms. Alkenyl of 60, substituted or unsubstituted cycloalkyl of 4 to 60 carbon atoms, substituted or unsubstituted aryl of 6 to 60 carbon atoms, or substituted or unsubstituted carbon atoms containing one or more of O, N, Si and S 2 to 60 heteroaryl,
x, y, and z are each independently integers from 1 to 20.
According to clause 12,
Containing 0.1 to 10 parts by weight of the compatibilizer based on 100 parts by weight of the biodegradable film,
Biodegradable film.
According to paragraph 1,
The biodegradable film has a yield tensile strength of 7 MPa or more, measured according to ASTM D882-07.
Biodegradable film.
According to paragraph 1,
The biodegradable film has a Young's modulus of 80 MPa or more, measured according to ASTM D882-07.
Biodegradable film.