US20230073319A1 - Improved thermoplastic condensate polymers and method to form them - Google Patents
Improved thermoplastic condensate polymers and method to form them Download PDFInfo
- Publication number
- US20230073319A1 US20230073319A1 US17/801,347 US202117801347A US2023073319A1 US 20230073319 A1 US20230073319 A1 US 20230073319A1 US 202117801347 A US202117801347 A US 202117801347A US 2023073319 A1 US2023073319 A1 US 2023073319A1
- Authority
- US
- United States
- Prior art keywords
- block
- chain extender
- condensation polymer
- block copolymer
- canceled
- 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
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F10/00—Additive manufacturing of workpieces or articles from metallic powder
- B22F10/10—Formation of a green body
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F10/00—Additive manufacturing of workpieces or articles from metallic powder
- B22F10/10—Formation of a green body
- B22F10/18—Formation of a green body by mixing binder with metal in filament form, e.g. fused filament fabrication [FFF]
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C64/00—Additive manufacturing, i.e. manufacturing of three-dimensional [3D] objects by additive deposition, additive agglomeration or additive layering, e.g. by 3D printing, stereolithography or selective laser sintering
- B29C64/10—Processes of additive manufacturing
- B29C64/106—Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material
- B29C64/118—Processes of additive manufacturing using only liquids or viscous materials, e.g. depositing a continuous bead of viscous material using filamentary material being melted, e.g. fused deposition modelling [FDM]
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C64/00—Additive manufacturing, i.e. manufacturing of three-dimensional [3D] objects by additive deposition, additive agglomeration or additive layering, e.g. by 3D printing, stereolithography or selective laser sintering
- B29C64/10—Processes of additive manufacturing
- B29C64/141—Processes of additive manufacturing using only solid materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C64/00—Additive manufacturing, i.e. manufacturing of three-dimensional [3D] objects by additive deposition, additive agglomeration or additive layering, e.g. by 3D printing, stereolithography or selective laser sintering
- B29C64/10—Processes of additive manufacturing
- B29C64/141—Processes of additive manufacturing using only solid materials
- B29C64/153—Processes of additive manufacturing using only solid materials using layers of powder being selectively joined, e.g. by selective laser sintering or melting
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B33—ADDITIVE MANUFACTURING TECHNOLOGY
- B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
- B33Y10/00—Processes of additive manufacturing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B33—ADDITIVE MANUFACTURING TECHNOLOGY
- B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
- B33Y70/00—Materials specially adapted for additive manufacturing
-
- 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
- C08G63/91—Polymers modified by chemical after-treatment
-
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/14—Lactams
-
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/14—Lactams
- C08G69/16—Preparatory processes
-
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/36—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino acids, polyamines and polycarboxylic acids
-
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/48—Polymers modified by chemical after-treatment
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing 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
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2067/00—Use of polyesters or derivatives thereof, as moulding material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2077/00—Use of PA, i.e. polyamides, e.g. polyesteramides or derivatives thereof, as moulding material
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/25—Process efficiency
Definitions
- the invention relates to condensate polymers and method to make them.
- the invention relates to cleaving of polycondensate polymers (e.g., polyamides and polyesters), capping of the cleaved polymers with a multifunctional end cap and reacting the multifunctional end cap with another compound that can undergo condensation.
- polycondensate polymers e.g., polyamides and polyesters
- Condensation polymers have been used to form shaped articles by traditional methods such as extrusion, film blowing, injection molding and the like. In these processes, the polymer is melted and substantially sheared resulting in cleaving of the polymer and uncontrolled loss of molecular weight causing deformation during forming of the shape (e.g., blow molded bottes and extruded tubes).
- a chain extender is added to reconstitute the molecular weight loss to realize sufficiently high melt strength and melt viscosity as described for polyester and polyethylene terephthalate in U.S. Pat. Nos. 4,246,378 and 7,544,387 respectively.
- thermoplastic polymers typically requires localized melting in layered patterns that then fuses and supports subsequent layers.
- Fused filament fabrication which is also commonly called plastic jetprinting has been used to form 3d parts by using thermo plastic filaments that are drawn into a nozzle heated, melted and then extruded where the extruded filaments fuse together upon cooling (see, for example, U.S. Pat. Nos. 5,121,329 and 5,503,785).
- selective laser sintering or melting has been used to make 3d parts by selectively sintering powders in a bed of powder (see, for example, U.S. Pat. No. 5,597,589).
- a bed of powder maintained at elevated temperatures is selectively sintered using a CO 2 laser or other electromagnetic radiation source.
- a further layer of powder is metered out and the selective sintering repeated until the desired 3d part is made. Since the powder must be sintered or melted, SLS has been limited to the use of thermoplastic polymers with very particular characteristics to allow for sintering without warping, slumping and achieving desired fusing particularly between layers. These requirements have tended to require the use a single type of polymer or highly compatible polymers when printing.
- the strength of the bonding within a layer and in particular between layers is typically lower than a part formed from a monolithic molded mass (e.g., injection molded). Because of the constraints dictated by the ability to localize heat, melt and regain sufficient strength to support the part being formed, the strength within a layer and between layers (referred to as strength in the Z direction or build direction) have been problematic in the use varying polymer together homogeneously within the part or heterogeneously in the part.
- condensation polymers that solves one or more of the problems in the art, such as allowing for the use of condensation polymer with limited compatibility to make additive manufactured articles or other shaped articles.
- a first aspect of the invention is a method of forming a chain extended condensation polymer comprising: (i) heating a condensation polymer in the presence of multifunctional chain extender to cause a portion of the condensation polymer to be cleaved to form a cleaved polymer having a cleaved end, wherein the chain extender reacts with at least a portion of the cleaved ends to form an end capped cleaved polycondensate polymer having an end cap that has at least one condensation reactive group, (ii) reacting a second compound having a reactive group that reacts with the end cap reactive group of the cleaved condensation polymer to form the chain extended condensation polymer, the second compound being different than the condensation polymer.
- the chain extender has a functionality of 1 (i.e., acts as an end cap for the capped cleaved polycondensate polymer), but the same chain extender has a functionality of 2 with another condensation polymer that can then react with the reactive functionality remaining in the chain extender capping the cleaved end capped condensation polymer.
- a second aspect of the invention is a block copolymer comprising a plurality of blocks and each block is a condensation polymer that is attached to another block through the residue of a chain extender with at least two blocks being chemically different.
- a third aspect of the invention is a branched block copolymer comprising, a plurality of blocks, each block being a condensation polymer and each block and branch is attached through the residue of a chain extender with at least one block or one branch being different than another branch or block of the branched block copolymer.
- a fourth aspect of the invention is a star condensation copolymer comprising a plurality of legs, wherein each leg is a condensation polymer that is attached through the residue of a chain extender with at least one leg being chemically different than another leg of the star copolymer.
- FIG. 1 is an illustration of the method to form a linear copolymer of the invention.
- FIG. 2 is an illustration of the method to form a star copolymer of this invention.
- FIG. 3 is another illustration of the method to form a star copolymer of this invention.
- FIG. 4 is an illustration of the method to form a branched copolymer of this invention.
- One or more as used herein means that at least one, or more than one, of the recited components may be used as disclosed. It is understood that the functionality of any ingredient or component may be an average functionality due to imperfections in raw materials, incomplete conversion of the reactants and formation of by-products.
- the method of the invention involves heating a condensation polymer sufficiently to cleave a portion of said polymer in the presence of a multifunctional chain extender.
- the chain extender reacts with the cleaved end.
- the multifunctional chain extender then reacts with a different second compound to form the chain extended polymer of this invention, which may be a block, graft or star polymer having one or more differing blocks.
- the method may be facilitated by shearing the condensation polymer.
- the condensation polymer may be any suitable condensation polymer such as those known in the art and commercially available.
- useful polymers include a polyamide, polyester, polycarbonate, polyamideimide, polyimide, polyacetal or combination thereof.
- the polymer is a polyamide, polyester, or polycarbonate.
- the condensation polymer may be linear or branched. Desirably, the condensation polymer is linear.
- polyamides include those available from Ube Industries Ltd., such as types Polyamide 6, Co polyamide (6/66), Co-polyamide (6/66/12), and Co-polyamide (6/12).
- polyesters include polyethylene terephthalate and other commercial polyesters such as those available from Celanese under the tradename CELANEX.
- polycarbonate include those available from Trinseo S.A. under the tradename CALIBRE.
- the condensation polymers have a weight average molecular weight (Mw) of greater than 1000, 10,000, 100,000 to 1,000,000 daltons.
- the condensation polymers have a melt flow rate (MFR) measured: [g/10 min.] 2.16 Kg @235° C. by a method prescribed by ASTM D1238 of 0.1 or 1 to 100, 50, 20 or 10.
- the multifunctional chain extender may have differing functionality depending on the particular condensation polymer used. Desirably, the functionality of the chain extender is from 1 or 2 to 5 with at least one of the condensation polymers and at least 2 to 4 with the second compound to realize the desired chain extension to for the chain extended condensation polymer. In a particular embodiment, the chain extender has a functionality of 1 (acts as an end cap) for the condensation polymer and a functionality of 2 or more with the second compounds (i.e., extends the condensation polymer with the second compound), which is further illustrated herein.
- the anhydrides which are particularly useful for end capping polyamides (functionality of 1), which is described in co-pending application filed concurrently having a title, CHAIN SCISSION TO MAKE IMPROVED POLYMERS FOR 3D PRINTING by Thomas Fry, et. al., incorporated herein by reference, may react with polyesters twice (functionality of 2).
- the chain extender may have 2 or more functional (reactive) groups with differing reactivity with a particular condensation polymer or differing reactivity with differing condensation polymers.
- the chain extender may be any useful for reacting and extending the condensation polymer and may vary depending on the particular condensation polymer.
- chain extender include those that are comprised of an epoxide, carboxylic acid, alcohol, anhydride, amines, isocyanate, aziridine, oxazoline, or phosphite ester or any combination thereof.
- the chain extender is comprised of a carboxylic acid, epoxide, anhydride or any combination thereof.
- the chain extender may have the ability to react with differing condensation polymers two or more times to extend the particular condensation polymer and or may be able to connect differing condensation polymers during the method.
- One or more multifunctional chain extender may be used, for example, to realize differing desired structures of the resulting chain extended condensation polymer.
- a small quantity of a higher functionality (e.g., 4-10 reactive groups) chain extender may be used with a large quantity of 2 functionality chain extender to realize structures such as a star polymer.
- epoxides may include solid epoxy resins such as those available under the tradename EPON from Miller-Stephenson and styrene based epoxide containing compounds available under the tradename JONCRYL from BASF.
- Other examples include epoxy thermoplastic elastomers.
- Additional examples include (poly) ethylene glycol diglycidylether, (poly)propylene glycol diglycidyl ether, polytetramethylene glycol diglycidyl ether, resorcin diglycidyl ether, neopentylglycol diglycidyl ether, 1,6-hexanediol diglycidylether, diglycidyl adipate, diglycidyl o-phthalate, diglycidyl terephthalate, hydroquinone diglycidyl ether, bisphenol S diglycidyl ether, glycerol diglycidyl ether, Sorbitol polyglycidyl ether, Sorbitan polyglycidyl ether, polyglycerol polyglycidyl ether, pentaerythritol polyglycidyl ether, diglycerolpolyglycidyl ether, triglycidyl tris(2-hydroxy
- Examples anhydrides may include pyromellitic dianhydride, benzophenonetetracarboxylic dianhydride, butane-1,2,3,4-tetracarboxylic dianhydride, maleic anhydride homopolymers, maleic anhydride-vinyl acetate copolymers, maleic anhydride-ethylene copolymers, maleic anhydride-isobutylene copolymers, maleic anhydride-isobutyl vinyl ether copolymers, maleic anhydride-acrylonitrile copolymers, maleic anhydride-styrene copolymers, tetrabromophthalic anhydride, hexahydrophthalic anhydride, trimellitic anhydride, 1,8-naphthalic anhydride, phthalic anhydride, or sulfophthalic anhydride, phenylenebisoxazoline, trimellitic dianhydride pyromellitic dianhydride, Bisphenol A-dig
- Illustrations of chain extenders displaying a functionality of 1 for polyamide and functionality of 2 for polyester include anhydrides having only one anhydride such as, but not limited to, phthalic anhydride, tetrabromophthalic anhydride, hexahydrophthalic anhydride, sulfophthalic anhydride, trimellitic anhydride, 1,8-naphthalic anhydride.
- the anhydride can ring open the anhydride leaving a carboxylic acid that can then be reacted with a polyester forming a chain extended block copolymer.
- the condensation polymer and chain extender are heated and sheared sufficiently to cleave at least a portion of the condensation and have the chain extender react with the cleaved end to form the end capped cleaved condensation polymer.
- the chain extender may react with terminal groups of the condensation polymer too and to cause some chain extension of the condensation polymer itself, so long as there is a portion of such end capped cleaved condensation polymer has an end cap having at least one further condensation reactive group that may react with the second compound.
- a portion may be any amount to realize the desired end capped cleaved condensation polymer and chain extended condensation polymer. Typically, a portion may be any amount from about 2 to 3, 10, 20, 50, 75 percent by number or weight to essentially all, with it being understood that all of the condensation polymer may be cleaved, end capped and extended.
- the second compound may be any desired compound to be incorporated into the condensation polymer of this invention.
- the second compound may be a compound that may react with one or more functional groups remaining in the residue of the chain extender capping the cleaved condensation polymer.
- the second compound may be other condensation polymers that are chemically different than the condensation polymer, which has been reacted with the chain extender. These second compounds of condensation polymers may be any of those described previously.
- the second compound may be an oligomer that is formed from a condensation reaction and has one or more chemical groups that may react with the chain extender reacted with the condensation polymer.
- the second compound may be a compound such as another chain extender that can react with the chain extender reacted with the condensation polymer adding further functionality to the condensation polymer reacted with the chain extender (in such cases, further extension may be subsequently by adding a further different second compound such as another condensation polymer).
- the heating to form the end capped cleaved condensation polymer may be any suitable method and apparatus for heating and mixing/shearing polymers such as those known in the art. Examples include high intensity mixers and screw extruders (e.g., single and twin screw extruders).
- the amount of shear may be any useful to facilitate the cleaving and end capping desired in a particular apparatus.
- the extruder may be held at one temperature or have a gradient along the length of the extruder to facilitate the cleaving and end capping desired.
- the temperature may be any that is sufficient to form the end capped cleaved condensation polymer, for example, just below the temperature where a particular condensation polymer starts to degrade.
- the temperature may be a temperature that is 100° C., 50° C., or 25° C. within the melting temperature of the condensation polymer. Typical temperatures may be from about 150° C., 175° C., or 200° C. to about 300° C. or 250° C.
- any temperature may be used to form the chain extended condensation polymer such as those just described.
- the shear may be any as typically used in the practice of compounding condensation polymers in compounding extruders.
- the time likewise may be any time sufficient to realize the desired chain extended condensation polymer. Typical times may be from 1 to 2 minutes to several hours (3-5) for reacting the chain extender with the cleaved condensation polymer or reacting with the second compound.
- FIG. 1 illustrates one embodiment of forming a linear block copolymer made by the method of this invention.
- Polyamide 1A is cleaved and forms polyamides PA1A and PA1B with PA1B being end capped by the chain extender (trimellitic anhydride depicted).
- These two new polyamides (PA1A and PA1B) of reduced molecular weight may form a linear block copolymer of alternating blocks of the initial two polyamides (PA1A and PA1B) by using a chain extender second compound (e.g., pyromellitic dianhydride).
- a branched or star block polymer may also be formed as described below.
- the PA1A may be a separately provide polyamide of differing chemistry or structure.
- two polymers of different types can be combined by selection of the appropriate end capping reactant and chain extender.
- This type of copolymerization can take place between any polycondensate pair provided, such as: polyamide/polyester, polyamide/polyimide, polyester/polycarbonate, and other combinations thereof with the appropriate chain extender and second compound, which may include a further chain extender and condensation polymer.
- the method may form novel and unique block copolymers comprised of a condensation polymer block that is attached to another block through the residue of a chain extender with at least two blocks being chemically different such as those condensation polymer pairs described above.
- the block copolymer has an alternating A-B block structure (e.g., A-B-A or A-B-A-B-A).
- a block is a polyamide and B block is polyester.
- the block copolymer may be any useful Mw.
- the block copolymer may be useful as compatibilizer and, in a particular embodiment, the block copolymer may be an insitu produced compatibilizer for unreacted condensation polymers remaining during the process of forming the block copolymer.
- FIG. 2 illustrates the formation of a star polymer.
- the polyamide in the illustration described above is heated and sheared in combination with a second compound comprised of a further chain extender pyromellitic dianhydride and a polyester as shown, which then forms a star polymer having three legs with one leg being polyamide and 2 legs being polyester.
- the method may form novel unique star polymers comprising a plurality of legs, wherein each leg is a condensation polymer that is attached through the residue of a chain extender with at least one leg being chemically different than another leg of the star copolymer.
- each leg of the star polymer has a molecular weight that is within 30% of the number average molecular weight (Mn) of all the legs.
- the star copolymer legs are comprised of a condensation polymer selected from the group consisting of polyamide, polyester, polycarbonate, polyamideimide, polyimide, or polyacetal.
- a condensation polymer selected from the group consisting of polyamide, polyester, polycarbonate, polyamideimide, polyimide, or polyacetal.
- at least one of the legs is a polyamide or polyester.
- Exemplary condensation polymer pairs that may make up the legs may be the same as those described above for the linear block copolymers.
- FIG. 3 illustrates a further route to make a star polymer, which may then be used as a cross-linker.
- FIG. 3 shows a polyamide that has been cleaved using aminophthalic anhydride.
- the two new polyamides of reduced molecular weight can be combined in the extrusion process by using a chain extender such as mellitic anhydride. Because most chains contain terminal amino groups, the primary reaction with the mellitic anhydride can be three functional. In this case, the three anhydrides are opened to bond with these terminal amino groups. Three free polyamide chains are able to be bound at this junction creating a large star like molecule. At the end of these three chains, a similar reaction can take place with additional chain extenders, resulting in a crosslinked system.
- a chain extender such as mellitic anhydride
- FIGS. 4 A and 4 B illustrates the formation of branch copolymer by the method of the invention.
- FIGS. 4 A and 4 B displays a reaction scheme for two different linear polyamides being used to develop one branched polyamide.
- Polyamide 1A refers to a polyamide of high molecular weight whereas Polyamide 2 is considered to be of low molecular weight.
- these polyamides are cleaved and end capped using aminophthalic anhydride and hydroxyphthalic anhydride, respectively.
- polyamides 1A and 1B are melt processed with dihydroxypyromellitic dianhydride resulting in a chain extension reaction between the amino end caps of the two polymers and the counter facing anhydride groups present on the chain extension molecule.
- the resulting polymer can then be melt processed with a chain extender like bisphenol-A diglycidyl ether (DGEBA) and polyamides 2A and 2B to encourage a second chain extension reaction.
- DGEBA bisphenol-A diglycidyl ether
- the epoxy groups on the chain extending molecule can form a covalent bond with the hydroxyl groups present on the dihydroxypyromellitic dianhydride.
- the remaining hydroxyl group from the DGEBA can then link with the hydroxyl and amino ends of polyamides 2A and 2B to form branches off the longer main polymer chain.
- the copolymerization and branching may allow the crystallization kinetics to be tuned.
- crystallization can be controlled by the ratio and selection of the two polymers used.
- Slow crystallizing segments such as those derived from a polyamide 12
- High temperature polyamides sections such as polyphthalamide
- amorphous polymer sections such as those from glycol modified polyethylene terephthalate, can be bound to a polyamide to slow or completely disrupt crystal growth.
- branching can be used to slow crystallization to a controlled extent.
- the length and amount of chains from polyamide 2A and 2B can be used to slow crystallization and decrease the degree of crystallinity.
- the free volume between chains can be increased. This increased free volume can disrupt crystal formation by preventing packing of the polyamide chains as well as by inhibiting the ability for the chain to reorient.
- This adjustment of crystallization can be highly controllable based on the selection of polymers to be placed in the backbone/branches as well as the concentration of chain extending molecule chosen to enable branching.
- the degree of crystallization for a given condensation polymer that is made into a branch or star polymer may be changed by about 10%, 20%, 30% 50% or more with all other things being essentially equal such as Mw, polydispersity, heating and cooling history.
- Mw molecular weight
- polydispersity molecular weight
- heating and cooling history a linear polyamide that is cleaved and formed into a branched polymer from the cleaved segments may realize such a change in degree of crystallization.
- the rheological properties may also vary by such amounts, for example, the MFR, as described herein may vary in a like manner.
Landscapes
- 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)
- Materials Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Life Sciences & Earth Sciences (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Exposure Of Semiconductors, Excluding Electron Or Ion Beam Exposure (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Laminated Bodies (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Graft Or Block Polymers (AREA)
- Polyamides (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Adhesives Or Adhesive Processes (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US17/801,347 US20230073319A1 (en) | 2020-02-26 | 2021-02-24 | Improved thermoplastic condensate polymers and method to form them |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US202062981937P | 2020-02-26 | 2020-02-26 | |
US202062981854P | 2020-02-26 | 2020-02-26 | |
US202062985007P | 2020-03-04 | 2020-03-04 | |
PCT/US2021/019405 WO2021173663A2 (en) | 2020-02-26 | 2021-02-24 | Improved thermoplastic condensate polymers and method to form them |
US17/801,347 US20230073319A1 (en) | 2020-02-26 | 2021-02-24 | Improved thermoplastic condensate polymers and method to form them |
Publications (1)
Publication Number | Publication Date |
---|---|
US20230073319A1 true US20230073319A1 (en) | 2023-03-09 |
Family
ID=74885073
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US17/801,344 Pending US20230097954A1 (en) | 2020-02-26 | 2021-02-24 | Method for improving adhesion in and between layers of additive manufactured articles |
US17/801,347 Pending US20230073319A1 (en) | 2020-02-26 | 2021-02-24 | Improved thermoplastic condensate polymers and method to form them |
US17/801,342 Pending US20230159703A1 (en) | 2020-02-26 | 2021-02-24 | Chain scission to make improved polymers for 3d printing |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US17/801,344 Pending US20230097954A1 (en) | 2020-02-26 | 2021-02-24 | Method for improving adhesion in and between layers of additive manufactured articles |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US17/801,342 Pending US20230159703A1 (en) | 2020-02-26 | 2021-02-24 | Chain scission to make improved polymers for 3d printing |
Country Status (7)
Country | Link |
---|---|
US (3) | US20230097954A1 (de) |
EP (3) | EP4110855A2 (de) |
JP (3) | JP2023514965A (de) |
KR (3) | KR20220123423A (de) |
CN (3) | CN115103869A (de) |
IL (3) | IL294900A (de) |
WO (3) | WO2021173651A1 (de) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20230340211A1 (en) | 2022-04-25 | 2023-10-26 | Jabil Inc. | Spherical particles for additive manufacturing |
WO2024063839A2 (en) | 2022-07-22 | 2024-03-28 | Jabil Inc. | Lead-free ammunition projectile |
CN117186388B (zh) * | 2023-08-01 | 2024-04-19 | 中山海明中科新材料有限公司 | 一种尼龙复合材料及其制备方法与应用 |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5592758A (en) | 1978-11-06 | 1980-07-14 | Toray Ind Inc | Resin composition |
ATE116179T1 (de) | 1986-10-17 | 1995-01-15 | Univ Texas | Verfahren und vorrichtung zur herstellung von formkörpern durch teilsinterung. |
US5121329A (en) | 1989-10-30 | 1992-06-09 | Stratasys, Inc. | Apparatus and method for creating three-dimensional objects |
US5503785A (en) | 1994-06-02 | 1996-04-02 | Stratasys, Inc. | Process of support removal for fused deposition modeling |
US20040176537A1 (en) * | 2001-10-16 | 2004-09-09 | Armentrout Rodney Scott | Inherently electrostatic dissipating block copolymer compositions |
EP2264095B1 (de) | 2004-10-20 | 2016-08-10 | The Chemours Company TT, LLC | Zusatzpackung für thermoplastische Kondensationspolymere |
JP2008523182A (ja) | 2004-12-13 | 2008-07-03 | ヘキソン スペシャルティ ケミカルズ インコーポレーテッド | ポリエステル樹脂の調製方法 |
CN101062981B (zh) * | 2006-04-26 | 2013-03-20 | 汕头大学 | 嵌段高分子材料及其制备方法 |
JP2011195815A (ja) | 2010-02-25 | 2011-10-06 | Toray Ind Inc | 熱可塑性樹脂組成物、その製造方法およびそれからなる成形品 |
US9744722B2 (en) * | 2012-11-21 | 2017-08-29 | Stratasys, Inc. | Additive manufacturing with polyamide consumable materials |
CN105408093B (zh) * | 2013-08-09 | 2018-09-25 | 金伯利-克拉克环球有限公司 | 用于三维印刷的聚合物材料 |
KR20180015725A (ko) * | 2015-06-03 | 2018-02-13 | 사빅 글로벌 테크놀러지스 비.브이. | 폴리이미드 전구체의 레이저-개시 적층 가공법 |
EP3526284B1 (de) * | 2016-10-17 | 2021-07-28 | L. Brüggemann GmbH & Co. KG | Additiv zur kontrollierten viskositätseinstellung von polymeren |
CN107652671B (zh) * | 2017-09-26 | 2021-06-01 | 湖南华曙高科技有限责任公司 | 基于聚酰胺的粉末合金材料及制备方法 |
-
2021
- 2021-02-24 KR KR1020227025958A patent/KR20220123423A/ko active Search and Examination
- 2021-02-24 KR KR1020227025956A patent/KR20220125269A/ko active Search and Examination
- 2021-02-24 WO PCT/US2021/019391 patent/WO2021173651A1/en active Search and Examination
- 2021-02-24 JP JP2022544107A patent/JP2023514965A/ja active Pending
- 2021-02-24 CN CN202180015011.5A patent/CN115103869A/zh active Pending
- 2021-02-24 US US17/801,344 patent/US20230097954A1/en active Pending
- 2021-02-24 IL IL294900A patent/IL294900A/en unknown
- 2021-02-24 WO PCT/US2021/019393 patent/WO2021173652A1/en active Search and Examination
- 2021-02-24 KR KR1020227025953A patent/KR20220124195A/ko active Search and Examination
- 2021-02-24 US US17/801,347 patent/US20230073319A1/en active Pending
- 2021-02-24 CN CN202180013917.3A patent/CN115943078A/zh active Pending
- 2021-02-24 JP JP2022544111A patent/JP7461484B2/ja active Active
- 2021-02-24 EP EP21712665.5A patent/EP4110855A2/de active Pending
- 2021-02-24 JP JP2022544110A patent/JP2023514966A/ja active Pending
- 2021-02-24 EP EP21712659.8A patent/EP4110618A1/de active Pending
- 2021-02-24 IL IL294899A patent/IL294899A/en unknown
- 2021-02-24 EP EP21712658.0A patent/EP4110854A1/de active Pending
- 2021-02-24 WO PCT/US2021/019405 patent/WO2021173663A2/en active Search and Examination
- 2021-02-24 IL IL294345A patent/IL294345A/en unknown
- 2021-02-24 CN CN202180013371.1A patent/CN115066455A/zh active Pending
- 2021-02-24 US US17/801,342 patent/US20230159703A1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
US20230159703A1 (en) | 2023-05-25 |
WO2021173652A1 (en) | 2021-09-02 |
US20230097954A1 (en) | 2023-03-30 |
EP4110855A2 (de) | 2023-01-04 |
IL294899A (en) | 2022-09-01 |
JP2023514965A (ja) | 2023-04-12 |
KR20220124195A (ko) | 2022-09-13 |
KR20220125269A (ko) | 2022-09-14 |
KR20220123423A (ko) | 2022-09-06 |
WO2021173663A3 (en) | 2021-09-30 |
JP2023514967A (ja) | 2023-04-12 |
CN115103869A (zh) | 2022-09-23 |
CN115943078A (zh) | 2023-04-07 |
EP4110618A1 (de) | 2023-01-04 |
EP4110854A1 (de) | 2023-01-04 |
WO2021173663A2 (en) | 2021-09-02 |
JP2023514966A (ja) | 2023-04-12 |
JP7461484B2 (ja) | 2024-04-03 |
IL294345A (en) | 2022-08-01 |
IL294900A (en) | 2022-09-01 |
WO2021173651A1 (en) | 2021-09-02 |
CN115066455A (zh) | 2022-09-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20230073319A1 (en) | Improved thermoplastic condensate polymers and method to form them | |
KR102466303B1 (ko) | 올레핀-말레산 무수물 공중합체들을 이용한 엔지니어링 플라스틱들의 변성 | |
CA1083295A (en) | Epoxy-catalyst additive system to produce higher i.v. polybutylene terephthalate from low i.v. polymer | |
EP0984027A1 (de) | Polyesterharz und verfahren zur herstellung eines geformten gegenstandes | |
US5902864A (en) | Process for the production of polyester resins | |
CA1124441A (en) | Copolyesters | |
KR20190038805A (ko) | 3d-프린팅된 물체를 생산하기 위한 열가소성 폴리에스테르 | |
US20020035218A1 (en) | Polyester resin and process for producing molded product thereof | |
KR20190035712A (ko) | 에어로졸 용기를 생산하기 위한 반결정질의 열가소성 폴리에스테르 | |
KR101405871B1 (ko) | 고분자량을 가지는 폴리에스테르 블렌드의 제조방법 및 이를 이용하여 제조된 폴리에스테르 블렌드 | |
CN112480580A (zh) | 一种水溶性生物降解高分子合金及其制备方法 | |
US6121387A (en) | Process for preparing a coating composition | |
EP0698059A1 (de) | Formkörper aus polyesterharzen | |
KR20210070313A (ko) | 폴리(1,4:3,6-디안하이드로헥시톨-코시클로헥실렌 테레프탈레이트) 유형의 폴리에스테르 제조 방법 | |
KR102249171B1 (ko) | 기계적 물성 및 가공성이 향상된 생분해성 수지 조성물 및 그로부터 제조되는 필름 | |
KR100323611B1 (ko) | 고수축성 폴리에스테르 블랜드의 제조방법 | |
EP0616623B1 (de) | Polymerlegierungen aus polyesterharzen und verfahren zu ihrer herstellung | |
KR20170112577A (ko) | 저융점 탄성 블록 공중합체, 이의 조성물, 및 이의 제조방법 | |
JP2023532477A (ja) | 3dプリントされた物体製造用の熱可塑性ポリエステル | |
RU1776680C (ru) | Термопластична полиамидна композици | |
JP2023532478A (ja) | 3dプリンティングされた物体を製造するための熱可塑性ポリエステル | |
JPH07252352A (ja) | 分岐ポリラクトンおよび分岐ポリラクトン組成物 | |
AU699697B2 (en) | Modified polymers | |
MXPA01002766A (en) | Production of improved polymers via the use of star cores | |
JPH09268254A (ja) | ポリエステルブロック共重合体組成物及びその製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: JABIL INC., FLORIDA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:FRY, THOMAS;LOESCH, LEVI;PETERSON, ZACHARY;AND OTHERS;REEL/FRAME:060898/0683 Effective date: 20220808 |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION |