Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
  • C08G63/06—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic 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
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
  • C08G63/06—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids
  • C08G63/08—Lactones or lactides
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/78—Preparation processes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
  • C08K5/0016—Plasticisers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
  • C08K5/005—Stabilisers against oxidation, heat, light, ozone
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
  • C08K5/0066—Flame-proofing or flame-retarding additives
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
  • C08K5/0083—Nucleating agents promoting the crystallisation of the polymer matrix
• • 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
  • C08K2201/00—Specific properties of additives
  • C08K2201/012—Additives improving oxygen scavenging properties
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L2201/00—Properties
  • C08L2201/06—Biodegradable
• • 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

Definitions

• This disclosure relates to biodegradable polymeric compositions. More particularly, this disclosure relates to biodegradable polymeric compositions which incorporate poly(3- hy droxy propi onate) .
• Biodegradable polymers are an area of increasing commercial interest.
• biodegradable polymers may be derived from renewable biomass resources, rather than from fossil fuels.
• biodegradable polymers products are biodegradable in many environments, in contrast to conventional nondegradable polymers which can take centuries to degrade after typical landfill or other disposal.
• PHAs poly(hydroxyalkanoates) or PHAs.
• PHAs are naturally-occurring biodegradable aliphatic polyesters are industrially produced by large-scale bacterial fermentation.
• the present disclosure provides a polymer composition.
• the polymer composition includes at least a first polymer and a second polymer.
• the first polymer is made up of at least 10 mole percent repeat units of (3-hydroxypropionate).
• the second polymer is made up of a poly(hydroxyalkanoate) which does not include repeat units of (3- hy droxy propi onate) .
• the first polymer is a copolymer or a terpolymer.
• This copolymer or terpolymer includes at least a first repeat unit which is (3-hydroxypropionate) and a second repeat unit according to Formula I
• the copolymer or terpolymer may also include a third repeat unit according to Formula II,
• R1 and R2 are each independently selected from the group consisting of linear or branched alkyl groups having from 1 to 22 carbon atoms.
• the polymer composition is preferably made up of about 1 to about 99 weight percent of the first polymer and from about 99 to about 1 weight percent of the second polymer. More preferably, the polymer composition is made up of from about 25 to about 75 weight percent of the first polymer and from about 75 to about 25 weight percent of the second polymer. Even more preferably, the polymer composition is made up of from about 40 to about 60 weight percent of the first polymer and from about 60 to about 40 weight percent of the second polymer.
• the polymer composition may also include at least one additional biopolymer, which is selected from the group consisting of polycaprolactone, poly(butylene succinate), poly(butylene succinate-co-butylene adipate), poly(lactic acid), poly(butylene adipate- co-terephtalate) and mixtures thereof.
• the polymer composition may include from about 5 to about 75 weight percent of the least one additional biopolymer.
• the second polymer is preferably made up of 2-hydroxyalkanoate repeat units, 3 -hydroxy alkanaoate repeat units, or 4-hydroxyalkanoate repeat units, each with or without branching from 1 carbon branches to 12 carbon branches.
• the second polymer is preferably made up of poly(3- hydroxybutyrate-co-3-hydroxyhexanoate) (“P(3HB-co-3HHx)”). More particularly, in some embodiments, this P(3HB-co-3HHx) is itself preferably made up of from about 75 to about 99 mole percent hydroxybutyrate repeat units and from about 1 to about 25 mole percent hydroxyhexanoate repeat units. Even more preferably, the P(3HB-co-3HHx) is made up of from about 93 to about 98 mole percent hydroxybutyrate repeat units and from about 2 to about 7 mole percent hydroxyhexanoate repeat units.
• P(3HB-co-3HHx) poly(3- hydroxybutyrate-co-3-hydroxyhexanoate)
• the polymer composition may also include various additives in addition to the aforementioned polymers.
• the polymer composition also preferably includes a nucleating agent selected from the group consisting of erythritols, pentaerythritol, dipentaerythritols, artificial sweeteners, stearates, sorbitols, mannitols, inositols, polyester waxes, nanoclays, behenamide, erucamide, stearamide, oleamide, poly(hydroxybutyrate), thymine, cyanuric acid, cytosine, adenine, uracil, guanine, boron nitride and mixtures thereof.
• a nucleating agent selected from the group consisting of erythritols, pentaerythritol, dipentaerythritols, artificial sweeteners, stearates, sorbitols, mannitols, inositols, polyester waxes, nanoclays, behenamide,
• the polymer composition also preferably includes a plasticizer selected from the group consisting of sebacates, citrates, fatty esters of adipic, succinic, and glucaric acids, lactates, alkyl diesters, citrates, alkyl methyl esters, dibenzoates, propylene carbonate, caprolactone diols having a number average molecular weight from 200- 10,000 g/mol, polyethylene glycols) having a number average molecular weight of 400 10,000 g/mol, esters of vegetable oils, long chain alkyl acids, adipates, glycerol, isosorbide derivatives or mixtures thereof, polymeric plasticizers, poly(hydroxyalkanoates) copolymers comprising at least 18 mole percent monomer residues of hydroxyalkanoates other than hydroxybutyrate, and mixtures thereof.
• a plasticizer selected from the group consisting of sebacates, citrates, fatty esters of adipic, succinic, and glu
• the polymer composition also preferably includes a filler selected from the group consisting of calcium carbonate, talc, nano clays, nanocellulose, hemp fibers, kaolin, carbon black, wollastonite, glass fibers, carbon fibers, graphite fibers , mica, silica, dolomite, barium sulfate, magnetite, halloysite, zinc oxide, titanium dioxide, montmorillonite, feldspar, asbestos, boron, steel, carbon nanotubes, cellulose fibers, flax, cotton, starch, polysaccharides, aluminum hydroxide, magnesium hydroxide, modified starches, chitins and chitosans, alginates, gluten, zein, casein, collagen, gelatin, polysaccharides, guar gum, xanthan gum, succinoglycan, natural rubbers; rosinic acid, lignins, natural fibers, jute, kenaf, hemp, ground nut shells,
• a filler selected
• the polymer composition also preferably includes an impact modifier selected from the group consisting of group consisting of acrylic-based resins and emulsions, isosorbide derivatives, natural rubbers, aliphatic polyesters, or mixtures thereof.
• the polymer composition preferably also includes at least one additive selected from the group consisting of lubricants, antioxidants, stabilizers, moisture scavengers, coupling agents, nucleators, or flame retardants.
• the first polymer and the second polymer may be further reacted with one another.
• the polymer composition preferably includes a catalyst or an initiator which induces reaction of the poly(3-hydroxypropionate) and the at least one additional poly(hydroxyalkanoate).
• the polymer composition thus also includes a reaction product formed from reaction the poly(3-hydroxypropionate) and the at least one additional poly(hydroxyalkanoate).
• the present disclosure also provides a converted article which is made up of the aforementioned polymer composition.
• the converted article may be selected from the group consisting of films, fibers, sheets, molded articles, rotomolded articles, extrusion blow molded articles, injection stretch blow molded articles, foams, melt coatings on substrates, and calendared sheets.
• the present disclosure also provides a method for making a poly(hydroxyalkanoate) copolymer or terpolymer.
• the methods includes a first step of combining:
• the method also includes a second step of polymerizing the reaction mixture to form a copolymer or terpolymer which comprises [027] a first repeat unit which is (3-hydroxypropionate),
• R1 and R2 are each independently selected from the group consisting of linear or branched alkyl groups having from 1 to 22 carbon atoms.
• the present disclosure first provides a novel polymer composition which includes at least a first polymer and a second polymer.
• the first polymer is made up of at least 10 mole percent repeat units of (3-hydroxypropionate).
• the second polymer is made up of a poly(hydroxyalkanoate) which does not include repeat units of (3-hydroxypropionate).
• the composition first includes a polymer which includes repeat units of (3- hydroxypropionate).
• the first polymer includes at least 10 mole percent repeat units of (3-hydroxypropionate).
• the first polymer may include from about 10 to about 99 mole percent of includes repeat units of (3-hydroxypropionate).
• the first polymer may include from about 25 to about 100 mole percent of includes repeat units of (3 -hy droxy propi onate) .
• the first polymer may be referred to simply as poly(3-hydroxypropionate).
• the first polymer may be a copolymer or even a terpolymer.
• this copolymer or terpolymer includes at least a first repeat unit which is (3-hydroxypropionate) and a second repeat unit according to Formula I
• the first polymer may also include a third repeat unit according to Formula II,
• R1 and R2 are each independently selected from the group consisting of linear or branched alkyl groups having from 1 to 22 carbon atoms.
• the polymer composition also includes a second polymer.
• This second polymer is a poly(hydroxyalkanoate) which does not include repeat units of (3-hydroxypropionate).
• the second polymer may, for instance, be made up of 2-hydroxyalkanoate repeat units, 3 -hydroxy alkanaoate repeat units, or 4- hydroxyalkanoate repeat units, each with or without branching from 1 carbon branches to 12 carbon branches.
• the second polymer is preferably made up of poly-3 -hydroxybutyrate- co-3-hydroxyhexanoate (“P(3HB-co-3HHx)”). More particularly, in some embodiments, this P(3HB-co-3HHx) is itself preferably made up of from about 75 to about 99 mole percent hydroxybutyrate repeat units and from about 1 to about 25 mole percent hydroxyhexanoate repeat units. Even more preferably, the P(3HB-co-3HHx) is made up of from about 93 to about 98 mole percent hydroxybutyrate repeat units and from about 2 to about 7 mole percent hydroxyhexanoate repeat units.
• P(3HB-co-3HHx) poly-3 -hydroxybutyrate- co-3-hydroxyhexanoate
• the relative amounts of the first polymer and the second polymer in the polymer composition may vary considerably.
• the polymer composition may be made up of about 1 to about 99 weight percent of the first polymer and from about 99 to about 1 weight percent of the second polymer.
• the polymer composition is made up of from about 25 to about 75 weight percent of the first polymer and from about 75 to about 25 weight percent of the second polymer. Even more preferably, the polymer composition is made up of from about 40 to about 60 weight percent of the first polymer and from about 60 to about 40 weight percent of the second polymer.
• the polymer composition may in some instances also include at least one additional biopolymer.
• This additional biopolymer may be selected from the group consisting of polycaprolactone, poly(butylene succinate), poly(butylene succinate-co-butylene adipate), poly(lactic acid), and mixtures thereof.
• the polymer composition may include from about 5 to about 75 weight percent of the least one additional biopolymer.
• the polymer composition may also include various additives in addition to the aforementioned polymers.
• the polymer composition may also include a nucleating agent selected from the group consisting of erythritols, pentaerythritol, dipentaerythritols, artificial sweeteners, stearates, sorbitols, mannitols, inositols, polyester waxes, nanoclays, behenamide, erucamide, stearamide, oleamide, poly(hydroxybutyrate), thymine, cyanuric acid, cytosine, adenine, uracil, guanine, boron nitride and mixtures thereof.
• a nucleating agent selected from the group consisting of erythritols, pentaerythritol, dipentaerythritols, artificial sweeteners, stearates, sorbitols, mannitols, inositols, polyester waxes, nanoclays, behenamide,
• the polymer composition may also include a plasticizer selected from the group consisting of sebacates, citrates, fatty esters of adipic, succinic, and glucaric acids, lactates, alkyl diesters, citrates, alkyl methyl esters, dibenzoates, propylene carbonate, caprolactone diols having a number average molecular weight from 200-10,000 g/mol, polyethylene glycols) having a number average molecular weight of 400-10,000 g/mol, esters of vegetable oils, long chain alkyl acids, adipates, glycerol, isosorbide derivatives or mixtures thereof, polymeric plasticizers, poly(hydroxyalkanoates) copolymers comprising at least 18 mole percent monomer residues of hydroxyalkanoates other than hydroxybutyrate, and mixtures thereof.
• a plasticizer selected from the group consisting of sebacates, citrates, fatty esters of adipic, succinic, and glu
• the polymer composition also preferably includes a filler selected from the group consisting of calcium carbonate, talc, nano clays, nanocellulose, hemp fibers, kaolin, carbon black, wollastonite, glass fibers, carbon fibers, graphite fibers , mica, silica, dolomite, barium sulfate, magnetite, halloysite, zinc oxide, titanium dioxide, montmorillonite, feldspar, asbestos, boron, steel, carbon nanotubes, cellulose fibers, flax, cotton, starch, polysaccharides, aluminum hydroxide, magnesium hydroxide, modified starches, chitins and chitosans, alginates, gluten, zein, casein, collagen, gelatin, polysaccharides, guar gum, xanthan gum, succinoglycan, natural rubbers; rosinic acid, lignins, natural fibers, jute, kenaf, hemp, ground nut shells,
• a filler selected
• the polymer composition also preferably includes an impact modifier selected from the group consisting of group consisting of acrylic-based resins and emulsions, isosorbide derivatives, natural rubbers, aliphatic polyesters, or mixtures thereof.
• the polymer composition preferably also includes at least one additive selected from the group consisting of lubricants, antioxidants, stabilizers, moisture scavengers, coupling agents, nucleators, or flame retardants.
• the polymer composition according to the present disclosure is typically prepared by blending, such as melt blending, of the first polymer and the second polymer, along with any other polymers or additives which may optionally be included in the composition.
• This blending can be accomplished using conventional melt blending techniques such as single screw extrusion, twin screw extrusion, or three roll mills.
• the first polymer and the second polymer may be further reacted with one another.
• the polymer composition preferably includes a catalyst or an initiator which induces reaction of the poly(3-hydroxypropionate) and the at least one additional poly(hydroxyalkanoate).
• the polymer composition thus also includes a reaction product formed from reaction the poly(3-hydroxypropionate) and the at least one additional poly(hydroxyalkanoate).
• the present disclosure also provides a method for making the poly(hydroxyalkanoate) copolymer or terpolymer discussed above. According to one embodiment, the methods include a first step of combining:
• R1 and R2 are each independently selected from the group consisting of linear or branched alkyl groups having from 1 to 22 carbon atoms.
• this mixture is then polymerized in a second step to form a copolymer or terpolymer.
• the polymerization reaction may be carried out at a reaction temperature from about 20 to about 120 C.
• a catalyst or initiator such as alkali metal or ammonium alkoxide, is also typically used to aid the polymerization.
• R1 and R2 are each independently selected from the group consisting of linear or branched alkyl groups having from 1 to 22 carbon atoms.
• the polymer composition prepared according to the present disclosure is industrially and/or home compostable, as determined by ASTM D6400.
• the present disclosure also provides a converted article which is made up of the aforementioned polymer composition.
• the converted article may be selected from the group consisting of films, fibers, sheets, molded articles, rotomolded articles, extrusion blow molded articles, injection stretch blow molded articles, foams, melt coatings on substrates, and calendared sheets.
• Embodiment 1 A polymer composition comprising a blend of a first polymer and a second polymer, wherein the first polymer comprises at least 10 mole percent repeat units of (3- hydroxypropionate) and the second polymer comprises a poly(hydroxyalkanoate) which does not include repeat units of (3-hydroxypropionate).
• Embodiment 2 The polymer composition of Embodiment 1, wherein the first polymer comprises poly(3 -hydroxypropionate).
• Embodiment 3 The polymer composition of Embodiment 1 or 2, wherein the first polymer comprises a copolymer or terpolymer, wherein the copolymer or terpolymer comprises
• R1 and R2 are each independently selected from the group consisting of linear or branched alkyl groups having from 1 to 22 carbon atoms.
• Embodiment 4 The polymer composition of any of the preceding Embodiments, wherein the polymer composition comprises from about 1 to about 99 weight percent of the first polymer and from about 99 to about 1 weight percent of the second polymer.
• Embodiment 5 The polymer composition of any of the preceding Embodiments, wherein the polymer composition comprises from about 25 to about 75 weight percent of the first polymer and from about 75 to about 25 weight percent of the second polymer.
• Embodiment 6 The polymer composition of any of the preceding Embodiments, wherein the polymer composition comprises from about 40 to about 60 weight percent of the first polymer and from about 60 to about 40 weight percent of the second polymer.
• Embodiment 7 The polymer composition of any of the preceding Embodiments, wherein the polymer composition further comprises at least one additional biopolymer selected from the group consisting of polycaprolactone, poly(butylene succinate), poly(butylene succinate-co- butylene adipate), poly(lactic acid), poly(butylene adipate-co-terephthalate) and mixtures thereof.
• additional biopolymer selected from the group consisting of polycaprolactone, poly(butylene succinate), poly(butylene succinate-co- butylene adipate), poly(lactic acid), poly(butylene adipate-co-terephthalate) and mixtures thereof.
• Embodiment 8 The polymer composition of Embodiment 7, wherein the polymer composition comprises from about 5 to about 75 weight percent of the least one additional biopolymer.
• Embodiment 9 The polymer composition of any of the preceding Embodiments, wherein the second polymer comprises 2-hydroxyalkanoate repeat units, 3 -hydroxy alkanaoate repeat units, or 4-hydroxyalkanoate repeat units, each with or without branching from 1 carbon branches to 12 carbon branches.
• Embodiment 10 The polymer composition of any of the preceding Embodiments, wherein the second polymer comprises poly-3 -hydroxybutyrate-co-3-hydroxyhexanoate (“P(3HB-co- 3HHx)”).
• Embodiment 11 The polymer composition of Embodiment 10, wherein the P(3HB-co- 3HHx) comprises from about 75 to about 99 mole percent hydroxybutyrate repeat units and from about 1 to about 25 mole percent hydroxyhexanoate repeat units.
• Embodiment 12 The polymer composition of Embodiment 10, wherein the P(3HB-co- 3HHx) preferably comprises from about 93 to about 98 mole percent hydroxybutyrate repeat units and from about 2 to about 7 mole percent hydroxyhexanoate repeat units.
• Embodiment 13 The polymer composition of any of the preceding Embodiments, further comprising a nucleating agent selected from the group consisting of erythritols, pentaerythritol, dipentaerythritols, artificial sweeteners, stearates, sorbitols, mannitols, inositols, polyester waxes, nanoclays, behenamide, erucamide, stearamide, oleamide, poly(hydroxybutyrate), thymine, cyanuric acid, cytosine, adenine, uracil, guanine, boron nitride and mixtures thereof.
• a nucleating agent selected from the group consisting of erythritols, pentaerythritol, dipentaerythritols, artificial sweeteners, stearates, sorbitols, mannitols, inositol
• Embodiment 14 The polymer composition of any of the preceding Embodiments, further comprising a plasticizer selected from the group consisting of sebacates, citrates, fatty esters of adipic, succinic, and glucaric acids, lactates, alkyl diesters, citrates, alkyl methyl esters, dibenzoates, propylene carbonate, caprolactone diols having a number average molecular weight from 200 10,000 g/mol, polyethylene glycols) having a number average molecular weight of 400 10,000 g/mol, esters of vegetable oils, long chain alkyl acids, adipates, glycerol, isosorbide derivatives or mixtures thereof, polymeric plasticizers, poly(hydroxyalkanoates) copolymers comprising at least 18 mole percent monomer residues of hydroxyalkanoates other than hydroxybutyrate, and mixtures thereof.
• a plasticizer selected from the group consisting of sebacates, citrates, fatty est
• Embodiment 15 The polymer composition of any of the preceding Embodiments, further comprising a filler selected from the group consisting of calcium carbonate, talc, nano clays, nanocellulose, hemp fibers, kaolin, carbon black, wollastonite, glass fibers, carbon fibers, graphite fibers , mica, silica, dolomite, barium sulfate, magnetite, halloysite, zinc oxide, titanium dioxide, montmorillonite, feldspar, asbestos, boron, steel, carbon nanotubes, cellulose fibers, flax, cotton, starch, polysaccharides, aluminum hydroxide, magnesium hydroxide, modified starches, chitins and chitosans, alginates, gluten, zein, casein, collagen, gelatin, polysaccharides, guar gum, xanthan gum, succinoglycan, natural rubbers; rosinic acid, lignins, natural fibers, jute, ken
• Embodiment 16 The polymer composition of any of the preceding Embodiments, further comprising an impact modifier selected from the group consisting of group consisting of acrylic- based resins and emulsions, isosorbide derivatives, natural rubbers, aliphatic polyesters, or mixtures thereof.
• an impact modifier selected from the group consisting of group consisting of acrylic- based resins and emulsions, isosorbide derivatives, natural rubbers, aliphatic polyesters, or mixtures thereof.
• Embodiment 17 The polymer composition of any of the preceding Embodiments, further comprising at least one additive selected from the group consisting of lubricants, antioxidants, stabilizers, moisture scavengers, coupling agents, nucleators, or flame retardants.
• Embodiment 18 The polymer composition of any of the preceding Embodiments, wherein the composition further comprises a catalyst or an initiator which induces reaction of the poly(3- hydroxypropionate) and the at least one additional poly(hydroxyalkanoate) and a reaction product formed from reaction the poly(3-hydroxypropionate) and the at least one additional poly(hydroxyalkanoate).
• Embodiment 19 A converted article comprising the polymer composition of any of the preceding Embodiments, wherein the converted article is selected from the group consisting of films, fibers, sheets, molded articles, rotomolded articles, extrusion blow molded articles, injection stretch blow molded articles, foams, melt coatings on substrates, and calendared sheets.
• Embodiment 20 A method for making a poly(hydroxyalkanoate) copolymer or terpolymer, comprising the steps of:
• R1 and R2 are each independently selected from the group consisting of linear or branched alkyl groups having from 1 to 22 carbon atoms.
• samples of poly(hydroxyalkanoate) compositions were compounded using a 40 mm twin screw extruder at the Danimer Polymer Development Center, in Bainbridge GA. Pentaerythritol was added to the samples at 1.0 weight percent to facilitate pelletization.
• the composition included only a poly(hydroxyalkanoate) (99 weight percent) and pentaerythritol (1 weight percent).
• the compositon was made up of about 89 weight percent of the same poly(hydroxyalkanoate), about 10 weight percnet of Poly(3-hydroxypropionate) (P3HP), and about 1 weight percent of pentaerythritol.
• the materials were processed at typical PHA process conditions for unknown R&D samples, with a target melt temperature of approximately 165 °C.
• the melt flow rate was measured at 175 °C using a 10 kg weight.
• Both the number average molecular weight (Mn) and the weight average molecular weight (Mw) of each sample was also measured using gel permeation chromatography using chloroform as a solvent. The results were as follows:

Landscapes

• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Crystallography & Structural Chemistry (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Biological Depolymerization Polymers (AREA)
• Polyesters Or Polycarbonates (AREA)
• Materials For Medical Uses (AREA)

Priority Applications (6)

Applications Claiming Priority (2)

Publications (1)

Family

ID=82942576

Family Applications (1)

Country Status (8)

Families Citing this family (2)

Citations (5)

Family Cites Families (4)

• 2022
  • 2022-07-29 KR KR1020247006455A patent/KR20240072126A/ko active Pending
  • 2022-07-29 CA CA3227351A patent/CA3227351A1/en active Pending
  • 2022-07-29 CN CN202280064124.9A patent/CN118355049A/zh active Pending
  • 2022-07-29 EP EP22757437.3A patent/EP4377374A1/en active Pending
  • 2022-07-29 JP JP2024505285A patent/JP2024527093A/ja active Pending
  • 2022-07-29 WO PCT/US2022/038762 patent/WO2023009773A1/en not_active Ceased
  • 2022-07-29 US US17/876,663 patent/US20230046792A1/en active Pending
  • 2022-07-29 AU AU2022319131A patent/AU2022319131A1/en active Pending

Patent Citations (5)

Also Published As

Similar Documents

Legal Events