EP3818099A1 - High pla content plastic material comprising a citrate ester - Google Patents
High pla content plastic material comprising a citrate esterInfo
- Publication number
- EP3818099A1 EP3818099A1 EP19734824.6A EP19734824A EP3818099A1 EP 3818099 A1 EP3818099 A1 EP 3818099A1 EP 19734824 A EP19734824 A EP 19734824A EP 3818099 A1 EP3818099 A1 EP 3818099A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- pla
- composition
- composition according
- chosen
- compatibilizer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/04—Polyesters derived from hydroxycarboxylic acids, e.g. lactones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L89/00—Compositions of proteins; Compositions of derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/08—Polymer mixtures characterised by other features containing additives to improve the compatibility between two polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/66—Substances characterised by their function in the composition
- C08L2666/68—Plasticizers; Solvents
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/062—Copolymers with monomers not covered by C08L33/06
- C08L33/068—Copolymers with monomers not covered by C08L33/06 containing glycidyl groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/08—Homopolymers or copolymers of acrylic acid esters
Definitions
- the present invention relates to a plastic composition based on biodegradable and biobased polyesters, in particular for the preparation of plastic films.
- Biobased and biodegradable films are known, based on starches or on derivatives of starches and polyesters, in particular monolayer or multilayer films, used in particular for the manufacture of plastic bags. These bags are used in particular for packaging food products, in particular fruit and vegetables.
- PLA polylactic acid
- PBAT polybutylene adipate terephthalate
- compatibilizers are known for this use, in particular polyacrylates, such as the products marketed under the names Joncryl® ADR (Dong & al., International Journal of Molecular Sciences, 2013, 14, 20189-20203; Ojijo & al., Polymer 2015 , 80, 1 -17; EP 1 699 872; EP 2 258 775; EP 2 679 633; WO 2013/164743; WO 2015/057694; US 7 448 510; US 2012/232191; US 7 368 503)
- the increase in the PLA content occurs at the expense of the mechanical properties of the products prepared with these polymer compositions.
- the films obtained with such compositions with a high PLA content and despite the addition of compatibilizing agent have reduced mechanical properties compared to films with less PLA, in particular in terms of elongation at break and of strength. tearing.
- increasing the PLA content in the compositions of the prior art does not make it possible to meet the specifications of the sacherie.
- the invention solves this technical problem by adding a particular plasticizer to the mixture of polyesters and compatibilizer.
- the invention relates to a plastic composition which comprises
- PLA polylactic acid
- a polyester chosen from PBAT (polybutylene adipate terephthalate), PHAs (polyhydroxyalkanoates), PBS (polybutylene succinate), PBSA (polybutylene succinate adipate) and their mixtures,
- a plasticizer chosen from citrate esters chosen from citrate esters.
- the invention also relates to a plastic film, the composition of which comprises a composition according to the invention, in particular obtained by extrusion of a composition according to the invention.
- the invention finally relates to a process for preparing a composition according to the invention which comprises at least the successive stages of mixing and melting with
- polyester chosen from PBAT (polybutylene adipate terephthalate), PHAs (polyhydroxyalkanoates), PBS (polybutylene succinate), PBSA (polybutylene succinate adipate) and their mixtures,
- plasticizer chosen from citrate esters which can be added at any time during the process.
- the invention relates to a plastic composition which comprises
- PLA polylactic acid
- a polyester chosen from PBAT (polybutylene adipate terephthalate), PHAs (polyhydroxyalkanoates), PBS (polybutylene succinate), PBSA (polybutylene succinate adipate) and their mixtures
- a plasticizer chosen from citrate esters chosen from citrate esters.
- compositions according to the invention are well known to those skilled in the art, in particular described in the publications, patents and patent applications mentioned above, in particular the polyesters and the PLA commonly used in the industry.
- biodegradable and / or biobased plastic materials in particular for the preparation of biobased and biodegradable films.
- PLA is formed from levorotatory lactic acid monomers (L) and / or dextrorotatory monomers (D), the level of monomers (L) and (D) can be variable.
- PLA can be a mixture of levorotatory PLA (PLLA), which is formed from predominantly monomers (L), and dextrorotatory PLA (PDLA), which is formed from predominantly monomers (D).
- the polyester b) is PBAT.
- PBAT is in the majority in the blend of polyesters other than PLA, preferably more than 60% of the blend, more preferably more from 70% even more preferably more than 80% by weight.
- polyester b) other than PLA is essentially PBAT, more preferably consists of only PBAT.
- the compatibilizers PLA / Polyesters are well known to those skilled in the art, in particular chosen from polyacrylates, terpolymers of ethylene, acrylic ester and glycidyl methacrylate (for example sold under the brand Lotader® by the company Arkema) , triblock copolymers PLA-PBAT-PLA, PLA grafted with maleic anhydride (PLA-g-AM) or PBAT grafted with maleic anhydride (PBAT-g-AM).
- the compatibilizer is chosen from polyacrylates, advantageously selected from methacrylate derivatives, preferably the compatibilizer is poly (ethylene-co-methyl acrylate-co-glycidyl methacrylate).
- the compatibilizer is poly (ethylene-co-methyl acrylate-co-glycidyl methacrylate).
- Such compatibilizers are well known and described in particular by Dong & al. (International Journal of Molecular Sciences, 2013, 14, 20189-20203) and Ojijo & al. (Polymer 2015, 80, 1 -17).
- a preferred compatibilizer is poly (ethylene-co-methyl acrylate-co-glycidyl methacrylate) sold under the name JONCRYL ADR-4468- ® by the company BASF.
- Citrate esters are also plasticizers known to those skilled in the art, in particular as bio-based materials. These include triethyl citrate (TEC), triethyl acetyl citrate (TEAC), tributyl citrate (TBC), tributyl acetyl citrate (TBAC).
- TEC triethyl citrate
- TEAC triethyl acetyl citrate
- TBAC tributyl citrate
- the citrate ester used as a plasticizer in the composition according to the invention is TBAC.
- the composition according to the invention comprises at least 25% of PLA, more preferably at least 28% of PLA, even more preferably at least 30% of PLA.
- the combination of the compatibilizer and the plasticizer used according to the invention and in particular the selection of citrate esters as plasticizers makes it possible to obtain PLA contents up to at least 35%, or even more, up to approximately 50% of PLA.
- the polyester content b) is advantageously at least 50% of the total weight of the composition. According to an advantageous embodiment of the invention, the polyester content b) is between 60 and 72%.
- the content of compatibilizer c) in the composition according to the invention is advantageously at least 0.1%, preferably from 0.4 to 2%, in particular 0.4, 0.5, or 1%, more preferably from 0.4 to 1.5%, advantageously approximately 0.4% by weight relative to the total weight of the composition.
- the content of citrate ester plasticizer d) in the composition according to the invention is advantageously at least 0.5%, preferably from 1 to 5%, more preferably from 2 to 4%, advantageously from approximately 3%, preferably about 2.5%.
- composition according to the invention may comprise other usual additives used in the composition of plastics, in particular for the preparation of films, such as mineral or organic fillers, pigments or dyes, etc.
- the composition according to the invention can comprise calcium carbonate.
- composition according to the invention comprises, relative to the total weight of the composition
- PLA polylactic acid
- a polyester chosen from PBAT (polybutylene adipate terephthalate), PHAs (polyhydroxyalkanoates), PBS (polybutylene succinate), PBSA (polybutylene succinate adipate) and their mixtures
- vs. between 0.4 to 1.5% of a PLA / Polyester compatibilizer chosen from polyacrylates, and d. between 2 to 4% of a plasticizer chosen from citrate esters.
- composition according to the invention can also comprise enzymes capable of degrading the polyesters so as to improve the biodegradability of the film according to the invention.
- the composition according to the invention can comprise enzymes capable of degrading the PLA.
- enzymes and their mode of incorporation into thermoplastic films are known to those skilled in the art, in particular described in patent applications WO 2013/093355, WO 2016/198652, WO 2016/198650, WO 2016/146540 and WO 2016/062695.
- these enzymes are chosen from proteases and serine proteases.
- the serine proteases are chosen from the Proteinase K of Tritirachium album, or the enzymes degrading the PLA originating from Amycolatopsis sp., Actinomadura keratinilytica, Laceyella sacchari LP175, Thermus sp., Or Bacillus licheniformis or commercial enzymes reformulated and known to degrade PLA such as Savinase®, Esperase®, Everlase® or any enzyme of the family of subtilisins CAS 9014-01 -1 or any functional variant.
- composition according to the invention also comprises enzymes degrading the polyesters, in particular degrading the PLA
- composition supplemented with enzymes is advantageously as follows:
- an enzymatic composition comprising from 0.0005 to 10% of enzyme associated with 50 to 95% of a polymer of low melting point and optionally associated with a stabilizing.
- This stabilizer can be chosen from polysaccharides, preferably from natural gums such as gum arabic.
- Said enzymatic composition can be prepared by extruding 50 to 95%, preferably 70 to 90%, of a low melting point polymer and 5 to 50%, preferably 10 to 30%, of a formulation liquid enzyme comprising from 0.01 to 35% of enzymes, from 19 to 60% preferably 19 to 65% of water and from 15 to 70% of stabilizer.
- a preferred enzymatic composition comprises in particular from 50 to 95% of a low melting point polymer, in particular polycaprolactone (PCL), preferably from 70 to 90%, from 0.001 to 10% of enzymes, preferably from 0.5 at 6%, or even 1 to 6%, and from 1.5 to 21% of gum arabic, preferably from 3 to 7%.
- PCL polycaprolactone
- plasticizer chosen from citrate esters
- the invention also relates to a process for the preparation of compositions according to the invention, with the compounds described above, with their proportions, comprising the steps of
- polyester chosen from PBAT (polybutylene adipate terephthalate), PHAs (polyhydroxyalkanoates), PBS (polybutylene succinate), PBSA (polybutylene succinate adipate) and their mixtures, at a temperature where the previously obtained mixture is partially or totally melted.
- PBAT polybutylene adipate terephthalate
- PHAs polyhydroxyalkanoates
- PBS polybutylene succinate
- PBSA polybutylene succinate adipate
- the plasticizer chosen from citrate esters can be added at any time during the process: at the time of step 1 with the PLA and the compatibilizer, between step 1 and step 2, at the time of step 2 with polyester or after step 2.
- the invention relates to a process for preparing a composition according to the invention comprising the steps of
- polyester chosen from PBAT (polybutylene adipate terephthalate), PHAs (polyhydroxyalkanoates), PBS (polybutylene succinate), PBSA (polybutylene succinate adipate) and their mixtures, at a temperature where the mixture previously obtained is partially or totally melted,
- PBAT polybutylene adipate terephthalate
- PHAs polyhydroxyalkanoates
- PBS polybutylene succinate
- PBSA polybutylene succinate adipate
- plasticizer chosen from citrate esters which can be carried out at any time during the process.
- the preparation of the composition is carried out according to the usual methods of the technique, in particular by extrusion.
- the extruded molten mixture is then cooled to form granules and is generally transformed into a final article of particular shape (films, flexible or solid parts).
- the articles prepared with the composition according to the invention also comprise enzymes degrading the polyesters as defined above, the latter are added either at the time of the preparation of the composition, or at the time of the preparation of the final articles by mixing granules of composition according to the invention, and the enzymes in a form suitable for their incorporation and according to the usual methods known to those skilled in the art.
- the latter will advantageously be used in the form of a suitable composition, which allows both the preservation and the transport of the enzymes, but also promotes their incorporation by preventing their degradation during this incorporation step.
- suitable compositions are known to those skilled in the art, and in particular described in patent applications WO 2019/043145 and WO 2019/043134.
- the addition of enzymes to the composition according to the invention can advantageously be carried out as follows: mixture between 80% and 98% of a composition according to the invention, with between 2% and 20% of a composition comprising an enzyme degrading the polyester and in particular the PLA, the percentages being given by weight relative to the weight of the final composition.
- the invention also relates to any article of plastic material made up or comprising elements made up of the composition according to the invention.
- the composition is in the form of granules prepared according to the usual techniques. These granules may be stored, transported, as granules used in the manufacture of plastic products, whatever their form and use, which can be called "final articles". They can be films, or flexible or solid parts of shapes and volumes adapted to their uses.
- the methods for preparing these final articles are well known to those skilled in the art, including in particular the usual techniques of plastics such as extrusion-inflation, extrusion-blowing, extrusion of cast film, calendering and thermoforming, injection molding, compression molding, rotational molding, coating, lamination, expansion, pultrusion, compression-granulation.
- plastics such as extrusion-inflation, extrusion-blowing, extrusion of cast film, calendering and thermoforming, injection molding, compression molding, rotational molding, coating, lamination, expansion, pultrusion, compression-granulation.
- Such operations are well known to those skilled in the art, who will easily adapt the conditions of the process as a function of the type of plastic articles provided (for example temperature, residence time, etc.).
- composition according to the invention is particularly suitable for the production of plastic films.
- the films according to the invention can be produced according to the usual methods of the technique, in particular by extrusion-inflation.
- the films can be prepared directly at the outlet of the extrusion die used for the preparation of the composition according to the invention, or also from granules of composition according to the invention which are melted according to the usual techniques, in particular by extrusion.
- the invention therefore also relates to a film of composition as defined above, with or without enzymes.
- the films according to the invention can be monolayer or multilayer films. In the case of a multilayer film, at least one of the layers has a composition as defined above.
- composition according to the invention is particularly suitable for being combined with enzymes degrading polyesters for the production of biodegradable plastic films.
- Plastic films, in particular monolayer films, of composition as defined above have both a high PLA content and retain mechanical properties as sought for the preparation of biodegradable and bio-based bags, in particular for packaging, films mulching, packaging of non-food or food products.
- compositions according to the invention will preferably be chosen from products compatible with food use.
- the films according to the invention advantageously have a thickness of less than 100 ⁇ m, more advantageously less than 50 ⁇ m, 40 ⁇ m or 30 ⁇ m, preferably less than 20 ⁇ m, in particular from 10 to 20 ⁇ m, more preferably from 6 to 20 ⁇ m.
- plastic films obtained with the composition according to the invention advantageously have the following properties,
- the elongation at break of the plastic film obtained with the composition according to the invention is advantageously at least 170%, in the longitudinal direction preferably at least 200%.
- the tear resistance of the plastic film obtained with the composition according to the invention is advantageously at least 35 N / mm in the transverse direction of the film, preferably at least 40 N / mm, more preferably at least 45 N / mm
- the plastic films obtained with the composition according to the invention also have the following properties,
- composition according to the invention can also be used for the production of rigid plastic products such as food packaging.
- compositions were produced on a Leistritz ZSE 18MAXX co-rotating twin-screw extruder. Solid materials such as polymers and compatibilizer were introduced using one or two gravimetric dosers depending on the composition. Indeed, for the compositions comprising the compatibilizer Joncryl® ADR 4468 C, first the PLA and compatibilizer mixture was introduced at the start of the extruder via a first dispenser, then the PBAT was introduced in a delayed manner via a second dispenser. For the compositions without compatibilizer, the PLA (4043D) and the PBAT (Ecoflex® C1200) were mixed and then introduced with a dispenser from the start of the extrusion. TBAC (Citrofol® BII) was introduced with a Brabender liquid pump from the start of extrusion. CaC03 was introduced with a gravimetric doser in zone 7/10.
- compositions were prepared under the same process conditions with a screw speed of 70 rpm and at a flow rate of 2 to 4 kg / h.
- the mixture of components arrives in the molten state in the last zone of the twin-screw which comprises a die with a hole with a diameter of 3.5 mm and is immediately immersed in a 2 m water tank and brought to a granulator to obtain cylindrical granules with a diameter of less than 3 mm.
- the granules obtained have the compositions described in table 2 (% by weight relative to the total weight of the composition)
- compositions 1 to 6 prepared in A) were used for the preparation of films.
- a LabTech LF-250 laboratory line, 20 mm wide, 30 L / D screw type LBE20-30 / C was used.
- the compositions were dried in a desiccator for 4 hours at 80 ° C.
- the screw speed was 60 rpm.
- the inflation rate was around 5.
- the films were then mechanically characterized in simple traction and in tearing using a Zwick test machine equipped with a 50 N sensor.
- the experimental conditions by type of test are summarized in Table 5.
- a “pants” type test piece is used for the tear test.
- the inventors established a specification to allow the films of the invention to be sold in the sack market, namely that it is desirable that the films of the invention reach the following values:
- Elongation at break which measures the ability of a material to lie under load before it breaks: 130% in the longitudinal direction and 240% in the transverse direction measured according to EN ISO 527-3.
- Tear resistance 40 N / mm in the transverse direction and measured according to the conditions of standard DIN EN ISO 6383 at 200 mm / min or under the conditions as described in this example.
- Elastic modulus 200 MPa in the longitudinal direction and 150 MPa in the transverse direction
- Maximum stress 15 MPa in the longitudinal direction and 13 MPa in the transverse direction
- All the films resulting from the invention have properties of elastic modulus and maximum stress not deteriorated compared to the films of the state of the art, and corresponding to the values requested by the specifications defined above.
- the granules were produced on a Clextral Evolum 25 HT co-rotating twin-screw.
- a PCM pump was used to dose the liquid TBAC.
- the PLA and Joncryl® mixture was introduced via a metering device at the start of the screw in the presence of the plasticizer TBAC. The mixture is melted and brought to the PBAT introduction area.
- the granules were prepared with a screw speed of 500 rpm and at a flow rate of 40 kg / h.
- the parameters used for the extrusion of the granules are presented in the table
- Table 8 The mixture of components arrives in the molten state in the Z12 screw and is immediately immersed in a 2.5 m water tank and brought to a granulator to obtain cylindrical granules with a diameter of less than 3 mm.
- compositions Three compositions are prepared, a composition 8 corresponding to the state of the art comprising 30% of PLA and 70% of PBAT, a composition 9 according to the invention comprising 30% of PLA, 66% of PBAT, 3% of T BAC and 1% of Joncryl® ADR 4468 C, and a composition 10 according to the invention comprising 35% of PLA, 60.3% of PBAT, 3.5% of TBAC and 1.2% of Joncryl® ADR 4468 C (% by weight relative to the total weight of the composition).
- the film 8 of composition 8 has an average thickness of 10 ⁇ m.
- Films 9 and 10 of compositions 9 and 10 have an average thickness of 14 ⁇ m. The thicknesses were measured with a micrometer.
- the films were then mechanically characterized in simple traction and in tear using a Lloyd LS5 testing machine equipped with a 20 N sensor and using the standards EN ISO 527-3 and EN ISO 6383-1. respectively.
- the experimental conditions by type of test are summarized in Table 9.
- a “pants” type test piece is used for the tear test.
- Films 9 and 10 according to the invention meet all the properties of the specifications defined by the inventors in example 1 part C), unlike film 8.
- composition 1 1 based on dibutyl sebacate (DBS) produced with the same compounding and extrusion-swelling processes as in Example 1 was produced for comparison.
- Composition 9 comprises 29% PLA, 67% PBAT, 3% DBS and 1% Joncryl® ADR 4468C.
- the film 1 1 corresponding to the composition 1 1 was characterized under the same conditions as the films of example 1 part D).
- the use of a conventional plasticizer such as DBS does not make it possible to meet all of the specifications defined by the inventors and adapted to the bag making market, the elongation at break in the transverse direction being less than 240% required and its breaking strength being less than 40 N / mm required.
- the granules were produced on a Clextral Evolum 25 HT co-rotating twin-screw.
- a PCM pump was used to dose the liquid TBAC.
- the PLA and Joncryl® mixture was introduced via a metering device at the start of the screw in the presence of the plasticizer TBAC. The mixture is melted and brought to the PBAT introduction area.
- the granules were prepared with a screw speed of 450 rpm and at a flow rate of 40 kg / h.
- the mixture of components arrives in the molten state in the screw in Z1 1 and is immediately granulated with an underwater cutting system to obtain half-moon granules with a diameter of less than 3 mm.
- compositions are prepared, a composition 12 according to the invention comprising 35% of PLA, 61, 1% of PBAT, 3.5% of TBAC and 0.4% of Joncryl® ADR 4468, a composition 13 according to the invention comprising 35% of PLA, 62.1% of PBAT, 2.5% of TBAC and 0.4% of Joncryl® ADR 4468, and a composition 14 according to the invention comprising 35% of PLA, 59.6% of PBAT, 2.5% TBAC 2.5% CaCO3 and 0.4% Joncryl® ADR 4468 (% by weight relative to the total weight of the composition).
- the granules prepared as described in A) were used for swelling extrusion with the same process and the same parameters described in example 1 part B).
- the film 12 of composition 12 has an average thickness of 13.7 ⁇ m.
- Films 13 and 14 of compositions 13 and 14 have an average thickness of 15 ⁇ m. The thicknesses were measured with a micrometer.
- the films were then mechanically characterized in simple traction and in tear using a Lloyd LS5 testing machine equipped with a 20 N sensor and using the standards EN ISO 527-3 and EN ISO 6383-1. respectively.
- the experimental conditions by type of test are summarized in Table 9 of Example 2.
- a “pants” type test piece is used for the tear test.
- Films 12, 13 and 14 according to the invention meet all of the properties of the specifications defined by the inventors.
- the addition of CaC03 slightly decreases the mechanical properties (elongation at break in the longitudinal direction and stress at break in both directions of measurement) while remaining within the specifications.
- the granules were produced on a Clextral Evolum 25 HT co-rotating twin-screw.
- a PCM pump was used to dose the liquid TBAC.
- the PLA and Joncryl® mixture was introduced via a metering device at the start of the screw in the presence of the plasticizer TBAC. The mixture is melted and brought to the PBAT introduction area.
- the granules were prepared with a screw speed of 450 rpm and at a flow rate of 40 kg / h.
- the mixture of components arrives in the molten state in the Z11 screw and is immediately granulated with an underwater cutting system to obtain half-moon granules with a diameter of less than 3 mm.
- a composition 15 is prepared according to the invention comprising 35% of PLA, 62.1% of PBAT, 2.5% of TBAC and 0.4% of Joncryl® ADR 4468
- the granules prepared as described in A) were used for the calendering film extrusion.
- a FAIREX extruder with a diameter of 45 mm, a flat die of 220 mm and adjustable lips fixed at 0.6 mm of opening were used as well as a three-cylinder calendering machine.
- the composition was dried for 4 hours at 80 ° C. in a desiccator.
- the calendered film 15 of composition 15 has an average thickness of 30 ⁇ m. The thicknesses were measured with a micrometer.
- the film was then mechanically characterized in simple traction and in tear using a Lloyd LS5 testing machine equipped with a 5 kN sensor and using the standards EN ISO 527-3 and EN ISO 6383-1. respectively.
- the experimental conditions by type of test are summarized in Table 9 of Example 2.
- a “pants” type test piece is used for the tear test.
- the inventors have established specifications to allow the film of the invention to be sold in the packaging market, namely that it is desirable for the film of the invention to reach the following values:
- Elongation at break which measures the capacity of a material to lie under load before it breaks: 10% in the longitudinal direction and measured according to standard EN ISO 527-3.
- Tear resistance 8 N / mm in the longitudinal direction and measured according to the conditions of DIN EN ISO 6383 at 200 mm / min or under the conditions as described in this example.
- the elastic module 400 MPa in the longitudinal direction
- the film 15 according to the invention meets all of the properties of the specifications defined by the inventors. This film has even more favorable properties, especially and especially in terms of elongation.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Biological Depolymerization Polymers (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1870810A FR3083543B1 (en) | 2018-07-06 | 2018-07-06 | HIGH PLA PLASTIC MATERIAL INCLUDING A CITRATE ESTER |
PCT/EP2019/068095 WO2020008029A1 (en) | 2018-07-06 | 2019-07-05 | High pla content plastic material comprising a citrate ester |
Publications (1)
Publication Number | Publication Date |
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EP3818099A1 true EP3818099A1 (en) | 2021-05-12 |
Family
ID=63312188
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19734824.6A Pending EP3818099A1 (en) | 2018-07-06 | 2019-07-05 | High pla content plastic material comprising a citrate ester |
Country Status (5)
Country | Link |
---|---|
US (1) | US11993705B2 (en) |
EP (1) | EP3818099A1 (en) |
CN (1) | CN112384554A (en) |
FR (1) | FR3083543B1 (en) |
WO (1) | WO2020008029A1 (en) |
Families Citing this family (4)
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CN110184851A (en) * | 2019-06-03 | 2019-08-30 | 武汉鑫亚泰科技有限公司 | A kind of degradable poly lactic acid dixie cup and preparation method thereof |
JP6916571B1 (en) | 2021-03-25 | 2021-08-11 | 株式会社Tbm | Resin composition and molded product |
CN113264835B (en) * | 2021-05-17 | 2023-06-16 | 河南正通食品科技有限公司 | Lactoyl citrate plasticizer and preparation method thereof |
CN113861636B (en) * | 2021-10-27 | 2023-01-03 | 佳易容聚合物(上海)有限公司 | High-stiffness high-toughness fully-degradable PBAT/PLA resin composition and preparation method thereof |
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ITTO20010057A1 (en) | 2001-01-25 | 2002-07-25 | Novamont Spa | BIODEGRADABLE POLYESTER TERNARY MIXTURES AND PRODUCTS OBTAINED FROM THESE. |
ITTO20010060A1 (en) | 2001-01-25 | 2002-07-25 | Novamont Spa | TERNARTIE MIXTURES OF BIODEGRADABLE ALIPHATIC POLYESTERS AND PRODUCTS OBTAINED FROM THESE. |
ITTO20010059A1 (en) | 2001-01-25 | 2002-07-25 | Novamont Spa | BIODEGRADABLE ALIPHATIC POLYESTER TERNARY MIXTURES AND PRODUCTS OBTAINED FROM THIS. |
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-
2018
- 2018-07-06 FR FR1870810A patent/FR3083543B1/en active Active
-
2019
- 2019-07-05 US US17/258,116 patent/US11993705B2/en active Active
- 2019-07-05 EP EP19734824.6A patent/EP3818099A1/en active Pending
- 2019-07-05 WO PCT/EP2019/068095 patent/WO2020008029A1/en unknown
- 2019-07-05 CN CN201980044850.2A patent/CN112384554A/en active Pending
Also Published As
Publication number | Publication date |
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FR3083543B1 (en) | 2021-03-05 |
WO2020008029A1 (en) | 2020-01-09 |
CN112384554A (en) | 2021-02-19 |
FR3083543A1 (en) | 2020-01-10 |
US20210284836A1 (en) | 2021-09-16 |
US11993705B2 (en) | 2024-05-28 |
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