Classifications

• • 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
  • C08L77/06—Polyamides derived from 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
  • C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
  • C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
  • C08G69/265—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids from at least two different diamines or at least two different dicarboxylic 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
  • C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
  • C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from 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
  • C08G69/02—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
  • 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
  • C08K5/0008—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
  • C08K5/04—Oxygen-containing compounds
  • C08K5/05—Alcohols; Metal alcoholates
  • C08K5/053—Polyhydroxylic alcohols
• • 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
  • C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
• • 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
  • C08K5/13—Phenols; Phenolates
• • 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
  • C08K5/16—Nitrogen-containing compounds
  • C08K5/17—Amines; Quaternary ammonium compounds
  • C08K5/18—Amines; Quaternary ammonium compounds with aromatically bound amino groups
• • 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
  • C08L67/03—Polyesters derived from dicarboxylic acids and dihydroxy compounds the dicarboxylic acids and dihydroxy compounds having the carboxyl- and the hydroxy groups directly linked to aromatic rings
• • 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
• • 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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
  • Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
  • Y10T428/139—Open-ended, self-supporting conduit, cylinder, or tube-type article

Definitions

• the present invention relates to the field of molded and extruded thermoplastic articles having improved long-term high temperature aging characteristics.
• High temperature resins based on polyamides possess desirable chemical resistance, processability and heat resistance. This makes them particularly well suited for demanding high performance applications including automotive and electrical/electronics applications.
• the mechanical properties generally tend to decrease due to the thermo-oxidation of the polymer. This phenomenon is called heat aging.
• heat stabilizers also referred as antioxidants
• examples of such heat stabilizers include hindered phenol antioxidants, amine antioxidants and phosphorus-based antioxidants.
• heat stabilizers include hindered phenol antioxidants, amine antioxidants and phosphorus-based antioxidants.
• polyamide compositions three types of heat stabilizers are conventionally used to retain the mechanical properties of the composition upon exposure to high temperatures.
• phenolic antioxidants optionally combined with a phosphorus based synergist as previously mentioned
• aromatic amines optionally combined with a phosphorus based synergist
• the third one is the use of copper salts and derivatives.
• Phenolic antioxidants are known to improve the mechanical/physical properties of the thermoplastic composition up to an aging temperature of 120° C.
• EP 1041109 discloses a polyamide composition
• a polyamide composition comprising a polyamide resin, a polyhydric alcohol having a melting point of 150 to 280° C., that has good fluidity and mechanical strength and is useful in injection welding techniques.
• Another problem is the heat ageing performance of polyamide compositions that generally have low levels of reinforcing agents or none at all. Since unreinforced compositions are generally used in applications that require some flexibility; an important attribute of unreinforced thermoplastics is the retention of strain at break upon heat ageing.
• thermoplastic article comprising a polyamide composition comprising
• high-temperature means a temperature of 150° C.
• long-term refers to an aging period equal or longer than 1000 hours (h).
• a polyamide composition, or a molded or extruded article therefrom is deemed to have “high heat stability” when 4 mm test specimens, as disclosed herein, when aged in an oven at an test temperature of 150° C. for a test period of 1000 h, in an atmosphere of air, and tested according to ISO 527-2/1A, have, on average, a retention of strain at break of greater than 80 percent, as compared with a control exposed at said test temperature for 72 h.
• the control herein is identical in composition and shape to that of the 2 mm test bar.
• (meth)acrylate is meant to include acrylate esters and methacrylate esters.
• the polyamide resin used in the present invention has a melting point and/or glass transition.
• melting points and glass transitions are as determined with differential scanning calorimetry (DSC) at a scan rate of 10° C./min in the first heating scan, wherein the melting point is taken at the maximum of the endothermic peak and the glass transition, if evident, is considered the mid-point of the change in enthalpy.
• Polyamides are condensation products of one or more dicarboxylic acids and one or more diamines, and/or one or more aminocarboxylic acids, and/or ring-opening polymerization products of one or more cyclic lactams. Suitable cyclic lactams are caprolactam and laurolactam. Polyamides may be fully aliphatic or semi-aromatic.
• Fully aliphatic polyamides used in the resin composition of the present invention are formed from aliphatic and alicyclic monomers such as diamines, dicarboxylic acids, lactams, aminocarboxylic acids, and their reactive equivalents.
• a suitable aminocarboxylic acid is 11-aminododecanoic acid.
• Suitable lactams are caprolactam and laurolactam.
• the term “fully aliphatic polyamide” also refers to copolymers derived from two or more such monomers and blends of two or more fully aliphatic polyamides. Linear, branched, and cyclic monomers may be used.
• Carboxylic acid monomers comprised in the fully aliphatic polyamides include, but are not limited to aliphatic carboxylic acids, such as for example adipic acid (C6), pimelic acid (C7), suberic acid (C8), azelaic acid (C9), decanedioic acid (C10), dodecanedioic acid (C12), tridecanedioic acid (C13), tetradecanedioic acid (C14), and pentadecanedioic acid (C15).
• aliphatic carboxylic acids such as for example adipic acid (C6), pimelic acid (C7), suberic acid (C8), azelaic acid (C9), decanedioic acid (C10), dodecanedioic acid (C12), tridecanedioic acid (C13), tetradecanedioic acid (C14), and pentadecanedi
• Diamines can be chosen among diamines having four or more carbon atoms, including, but not limited to tetramethylene diamine, hexamethylene diamine, octamethylene diamine, decamethylene diamine, dodecamethylene diamine, 2-methylpentamethylene diamine, 2-ethyltetramethylene diamine, 2-methyloctamethylenediamine; trimethylhexamethylenediamine, meta-xylylene diamine, and/or mixtures thereof.
• the semi-aromatic polyamide is a homopolymer, a copolymer, a terpolymer or more advanced polymers formed from monomers containing aromatic groups.
• One or more aromatic carboxylic acids may be terephthalate or a mixture of terephthalate with one or more other carboxylic acids, such as isophthalic acid, phthalic acid, 2-methyl terephthalic acid and naphthalic acid.
• the one or more aromatic carboxylic acids may be mixed with one or more aliphatic dicarboxylic acids, as disclosed above.
• an aromatic diamine such as meta-xylylene diamine (MXD) can be used to provide a semi-aromatic polyamide, an example of which is MXD6, a homopolymer comprising MXD and adipic acid.
• MXD meta-xylylene diamine
• Preferred polyamides disclosed herein are homopolymers or copolymers wherein the term copolymer refers to polyamides that have two or more amide and/or diamide molecular repeat units.
• the homopolymers and copolymers are identified by their respective repeat units.
• the repeat units are listed in decreasing order of mole % repeat units present in the copolymer. The following list exemplifies the abbreviations used to identify monomers and repeat units in the homopolymer and copolymer polyamides (PA):
• the term “6” when used alone designates a polymer repeat unit formed from -caprolactam.
• the “6” when used in combination with a diacid such as T, for instance 6T, the “6” refers to HMD.
• the diamine In repeat units comprising a diamine and diacid, the diamine is designated first.
• the first “6” refers to the diamine HMD, and the second “6” refers to adipic acid.
• repeat units derived from other amino acids or lactams are designated as single numbers designating the number of carbon atoms.
• Polyamides may have semiaromatic repeat units to the extent that the melting point is less than 210° C. and generally the semiaromatic polyamides of the group have less than 40 mole percent semiaromatic repeat units.
• Semiaromatic repeat units are defined as those derived from monomers selected from one or more of the group consisting of: aromatic dicarboxylic acids having 8 to 20 carbon atoms and aliphatic diamines having 4 to 20 carbon atoms.
• One embodiment is a molded or extruded thermoplastic article wherein said polyamide resin is selected from Group (I) Polyamides and wherein said test temperature is at least 150° C. for a test period of at least 1000 hours and said retention of strain is greater than 80%.
• said polyamide resin is selected from Group (I) Polyamides and wherein said test temperature is at least 150° C. for a test period of at least 1000 hours and said retention of strain is greater than 80%.
• One embodiment is a molded or extruded thermoplastic article wherein said polyamide resin is selected from Group (II) Polyamides and wherein said test temperature is at least 150° C. for a test period of at least 1000 hours and said retention of strain is greater than 80%.
• said polyamide resin is selected from Group (II) Polyamides and wherein said test temperature is at least 150° C. for a test period of at least 1000 hours and said retention of strain is greater than 80%.
• polyamide resin is selected from Group (III)
• Polyamides are selected from the group consisting of poly(tetramethylene hexanediamide/tetramethylene terephthalamide) (PA46/4T), poly(tetramethylene hexanediamide/hexamethylene terephthalamide) (PA46/6T), poly(tetramethylene hexanediamide/2-methylpentamethylene hexanediamide/decamethylene terephthalamide)_PA46/D6/10T), poly(hexamethylene hexanediamide/hexamethylene terephthalamide) (PA66/6T), poly(hexamethylene hexanediamide/hexamethylene isophthalamide/hexamethylene terephthalamide PA66/6I/6T, and poly(hexamethylene hexanediamide/2-methylpentamethylene hexanediamide/hexamethylene terephthalamide
• polyamide resin is selected from Group (IV) Polyamides selected from the group consisting of poly(tetramethylene terephthalamide/hexamethylene hexanediamide) (PA4T/66), poly(tetramethylene terephthalamide/ ⁇ -caprolactam) (PA4T/6), poly(tetramethylene terephthalamide/hexamethylene dodecanediamide) (PA4T/612), poly(tetramethylene terephthalamide/2-methylpentamethylene hexanediamide/hexamethylene hexanediamide) (PA4T/D6/66), poly(hexaamethylene terephthalamide/2-methylpentamethylene terephthalamide/hexamethylene hexanediamide) (PA6T/DT/66), poly(hexamethylene terephthalamide/hexamethylene hexanediamide) PA6T/66, poly(hexamethylene terephthalamide/hexamethylene hexan
• polyamide resin is selected from Group (V) Polyamides selected from the group consisting of poly(tetramethylene terephthalamide/2-methylpentamethylene terephthalamide) PA4T/DT, poly(tetramethylene terephthalamide/hexamethylene terephthalamide) PA4T/6T, poly(tetramethylene terephthalamide/decamethylene terephthalamide) PA4T/10T, poly(tetramethylene terephthalamide/dodecamethylene terephthalamide)PA4T/12T, poly(tetramethylene terephthalamide/2-methylpentamethylene terephthalamide/hexamethylene terephthalamide) (PA4T/DT/6T), poly(tetramethylene terephthalamide/hexamethylene terephthalamide/2-methylpentamethylene terephthalamide) (PA4T/6T/DT), poly(hexamethylene terephthalamide resin is selected from Group (V) Polyamides selected from the group consisting
• the polyamide is a Group (III) Polyamide, Group (IV) Polyamide, Group (V) Polyamide or Group (VI) Polyamide, respectively.
• the polyamides may also be blends of two or more polyamides.
• Preferred blends include those selected from the group consisting of Group (I) and Group (II) Polyamides; Group (I) and (III) Polyamide, Group (I) and Group (VI) Polyamides, Group (II) and Group (III) Polyamides, Group (II) and Group (IV) Polyamides, Group (II) and Group (V) Polyamides, Group (II) and Group (VI) Polyamides, Group (III) and Group (VI) Polyamides, and Group (IV) and Group (V) Polyamides.
• a preferred blend includes Group (II) and Group (V) Polyamides, and a specific preferred blend includes poly(hexamethylene hexanediamide) (PA 66) and poly(hexamethylene terephthalamide/2-methylpentamethylene terephthalamide) (PA 6T/DT).
• Another preferred blend includes Group (II) and Group (III) Polyamides and a specific preferred blend includes poly( ⁇ -caprolactam) (PA6) and poly(hexamethylene hexanediamide/hexamethylene terephthalamide (PA66/6T).
• PA6 poly( ⁇ -caprolactam)
• PA66/6T poly(hexamethylene hexanediamide/hexamethylene terephthalamide
• the molded or extruded thermoplastic article comprises 0.1 to 10 weight percent of one or more polyhydric alcohols having more than two hydroxyl groups and having a number average molecular weight (M n ) of less than 2000 as determined for polymeric materials with gel permeation chromatography (GPC).
• M n number average molecular weight
• Polyhydric alcohols may be selected from aliphatic hydroxylic compounds containing more than two hydroxyl groups, aliphatic-cycloaliphatic compounds containing more than two hydroxyl groups, cycloaliphatic compounds containing more than two hydroxyl groups, aromatic and saccharides.
• An aliphatic chain in the polyhydric alcohol can include not only carbon atoms but also one or more hetero atoms which may be selected, for example, from nitrogen, oxygen and sulphur atoms.
• a cycloaliphatic ring present in the polyhydric alcohol can be monocyclic or part of a bicyclic or polycyclic ring system and may be carbocyclic or heterocyclic.
• a heterocyclic ring present in the polyhydric alcohol can be monocyclic or part of a bicyclic or polycyclic ring system and may include one or more hetero atoms which may be selected, for example, from nitrogen, oxygen and sulphur atoms.
• the one or more polyhydric alcohols may contain one or more substituents, such as ether, carboxylic acid, carboxylic acid amide or carboxylic acid ester groups.
• polyhydric alcohol containing more than two hydroxyl groups include, without limitation, triols, such as glycerol, trimethylolpropane, 2,3-di-(2′-hydroxyethyl)-cyclohexan-1-ol, hexane-1,2,6-triol, 1,1,1-tris-(hydroxymethyl)ethane, 3-(2′-hydroxyethoxy)-propane-1,2-diol, 3-(2′-hydroxypropoxy)-propane-1,2-diol, 2-(2′-hydroxyethoxy)-hexane-1,2-diol, 6-(2′-hydroxypropoxy)-hexane-1,2-diol, 1,1,1-tris-[(2′-hydroxyethoxy)-methyl]-ethane, 1,1,1-tris-[(2′-hydroxypropoxy)-methyl]-propane, 1,1,1-tris-(4′-hydroxyphenyl)-ethane, 1,1,1,
• Preferred polyhydric alcohols include those having a pair of hydroxyl groups which are attached to respective carbon atoms which are separated one from another by at least one atom.
• Especially preferred polyhydric alcohols are those in which a pair of hydroxyl groups is attached to respective carbon atoms which are separated one from another by a single carbon atom.
• the polyhydric alcohol used in the thermoplastic composition is pentaerythritol, dipentaerythritol, tripentaerythritol, di-trimethylolpropane, D-mannitol, D-sorbitol and xylitol. More preferably, the polyhydric alcohol used is dipentaerythritol and/or tripentaerythritol. A most preferred polyhydric alcohol is dipentaerythritol.
• the content of said polyhydric alcohol in the thermoplastic composition is 0.1 to less than 10 weight percent, preferably 0.25-8 weight percent, more preferably 0.25-5 weight percent and most preferably 1-4 weight percent; based on the total weight of said thermoplastic composition.
• the molded or extruded thermoplastic article comprises less than 10 weight percent, preferably 5 weight percent % or less of one or more reinforcement agents.
• the molded or extruded thermoplastic article includes no reinforcement agent.
• a reinforcement agent may be any filler, but is preferably selected from the group consisting calcium carbonate, glass fibers with circular and noncircular cross-section, glass flakes, glass beads, carbon fibers, talc, mica, wollastonite, calcined clay, kaolin, diatomite, magnesium sulfate, magnesium silicate, barium sulfate, titanium dioxide, sodium aluminum carbonate, barium ferrite, potassium titanate and mixtures thereof.
• the molded or extruded thermoplastic article may further comprise 0 to 50 weight percent of a polymeric toughener comprising a reactive functional group and/or a metal salt of a carboxylic acid.
• the molded or extruded thermoplastic article comprises 2 to 20 weight percent polymeric toughener selected from the group consisting of: a copolymer of ethylene, glycidyl(meth)acrylate, and optionally one or more (meth)acrylate esters; an ethylene/ ⁇ -olefin or ethylene/ ⁇ -olefin/diene copolymer grafted with an unsaturated carboxylic anhydride; a copolymer of ethylene, 2-isocyanatoethyl(meth)acrylate, and optionally one or more (meth)acrylate esters; and a copolymer of ethylene and acrylic acid reacted with a Zn, Li, Mg or Mn compound to form the corresponding ionomer.
• the molded or extruded thermoplastic article comprises 0 to 3 weight percent of a co-stabilizer that is useful in combination with the polyhdric alcohol, in affecting the long-term heat stability of article.
• a co-stabilizer that is useful in combination with the polyhdric alcohol, in affecting the long-term heat stability of article.
• Preferred co-stabilizers have a 10% weight loss temperature, as determined by TGA, of greater than 30° C. below said melting point of said polyamide if said melting point is present, or at least 250° C. if said melting point is not present; and said co-stabilizers are selected from the group consisting of secondary aryl amines, hindered amine light stabilizers, and mixtures thereof.
• TGA weight loss will be determined according to ASTM D 3850-94, using a heating rate of 10° C./min, in air purge stream, with an appropriate flow rate of 0.8 mL/second.
• the co-stabilizer preferably has a 10% weight loss temperature, as determined by TGA, of at least 270° C., and more preferably 290° C., 320° C., and 340° C., and most preferably at least 350° C.
• the one or more co-stabilizers preferably are present from at or about 0.1 to 3 weight percent, and more preferably at or about 0.1 to at or about 1 weight percent, or more preferably from at or about 0.1 to at or about 0.7 weight percent, based on the total weight of the polyamide composition.
• Secondary aryl amines useful in the invention are high molecular weight organic compound having low volatility.
• the high molecular weight organic compound will be selected from the group consisting of secondary aryl amines further characterized as having a molecular weight of at least 260 g/mol and preferably at least 350 g/mol, together with a 10% weight loss temperature as determined by TGA of at least 290° C., preferably at least 300° C., 320° C., 340° C., and most preferably at least 350° C.
• secondary aryl amine an amine compound that contains two carbon radicals chemically bound to a nitrogen atom where at least one, and preferably both carbon radicals, are aromatic.
• aromatic substituents such as, for example, a phenyl, naphthyl or heteroaromatic group, is substituted with at least one substituent, preferably containing 1 to about 20 carbon atoms.
• suitable secondary aryl amines include 4,4′di( ⁇ , ⁇ -dimethylbenzyl)diphenylamine available commercially as Naugard 445 from Uniroyal Chemical Company, Middlebury, Conn.; the secondary aryl amine condensation product of the reaction of diphenylamine with acetone, available commercially as Aminox from Uniroyal Chemical Company; and para-(paratoluenesulfonylamido)diphenylamine also available from Uniroyal Chemical Company as Naugard SA.
• Other suitable secondary aryl amines include N,N ⁇ -di-(2-naphthyl)-p-phenylenediamine, available from ICI Rubber Chemicals, Calcutta, India.
• Suitable secondary aryl amines include 4,4′-bis( ⁇ , ⁇ ′-tertiaryoctyl)diphenylamine, 4,4′-bis( ⁇ -methylbenzhydryl)diphenylamine, and others from EP 0509282 B1.
• the molded or extruded thermoplastic article may have at least one co-stabilizer selected from one or more secondary aryl amines.
• the one or more secondary aryl amines is present at about 0.25 to 1.0 weight percent and more preferably 0.25 to about 0.9 weight percent, based on the total weight of the polyamide composition.
• HALS hindered amine light stabilizers
• HALS are compounds of the following general formulas and combinations thereof:
• R 1 up to and including R 5 are independent substituents.
• suitable substituents are hydrogen, ether groups, ester groups, amine groups, amide groups, alkyl groups, alkenyl groups, alkynyl groups, aralkyl groups, cycloalkyl groups and aryl groups, in which the substituents in turn may contain functional groups; examples of functional groups are alcohols, ketones, anhydrides, imines, siloxanes, ethers, carboxyl groups, aldehydes, esters, amides, imides, amines, nitriles, ethers, urethanes and any combination thereof.
• a hindered amine light stabilizer may also form part of a polymer or oligomer.
• the HALS is a compound derived from a substituted piperidine compound, in particular any compound derived from an alkyl-substituted piperidyl, piperidinyl or piperazinone compound, and substituted alkoxypiperidinyl compounds.
• Examples of such compounds are: 2,2,6,6-tetramethyl-4-piperidone; 2,2,6,6-tetrametyl-4-piperidinol; bis-(1,2,2,6,6-pentamethyl piperidyl)-(3′,5′-di-tert-butyl-4′-hydroxybenzyl)butylmalonate; di-(2,2,6,6-tetramethyl-4-piperidyl)sebacate (Tinuvin® 770, MW 481); oligomer of N-(2-hydroxyethyl)-2,2,6,6-tetramethyl-4-piperidinol and succinic acid (Tinuvin® 622); oligomer of cyanuric acid and N,N-di(2,2,6,6-tetramethyl-4-piperidyl)-hexamethylene diamine; bis-(2,2,6,6-tetramethyl-4-piperidinyl)succinate; bis-(1-octyloxy-2,2,6,
• Tinuvin® and Chimassorb® materials are available from Ciba Specialty Chemicals; Cyasorb® materials are available from Cytec Technology Corp.; Uvasil® materials are available from Great Lakes Chemical Corp.; Saduvor®, Hostavin®, and Nylostab® materials are available from Clariant Corp.; Uvinul® materials are available from BASF; Uvasorb® materials are available from Partecipazioni Industriali; and Good-rite® materials are available from B.F. Goodrich Co. Mark® materials are available from Asahi Denka Co.
• Preferred HALS include high-molecular weight oligomeric or polymeric HALS having a molecular weight of more than about 1000, and preferably more than about 2000.
• HALS are selected from the group consisting or di-(2,2,6,6-tetramethyl-4-piperidyl)sebacate (Tinuvin® 770, MW 481) Nylostab® S-EED (Clariant Huningue S.
• the molded or extruded thermoplastic article may have at least one co-stabilizer selected from one or more HALS.
• the one or more HALS is present at about 0.25 to 1.0 weight percent and more preferably 0.25 to about 0.9 weight percent, based on the total weight of the polyamide composition.
• a preferred embodiment comprises at least two co-stabilizers, at least one selected from the secondary aryl amines; and at least one selected from the group of HALS, as disclosed above, wherein the total weight percent of the mixture of co-stabilizers is at least 0.5 weight percent, and preferably at least 0.9 weight percent.
• the polyamide composition may also comprise other additives commonly used in the art, such as other heat stabilizers or antioxidants, antistatic agents, blowing agents, lubricants, plasticizers, and colorant and pigments.
• additives commonly used in the art, such as other heat stabilizers or antioxidants, antistatic agents, blowing agents, lubricants, plasticizers, and colorant and pigments.
• heat stabilizers include copper stabilizers and hindered phenols, and mixtures thereof.
• thermoplastic articles of the invention A significant advantage of the molded or extruded thermoplastic articles of the invention is that high thermal stability, as measured under AOA conditions disclosed herein, is provided without the use of conventional copper heat stabilizers. Copper heat stabilizers tend to act as corrosive agents over long periods of time at elevated temperatures; and in some environments actually cause degradation of semiaromatic polymers.
• another embodiment is molded or extruded thermoplastic article wherein said polyamide composition comprises less than 25 ppm copper as determined with atomic absorption spectroscopy.
• the polyamide composition may comprise plasticizers.
• a plasticizer will preferably be miscible with the polyamide.
• suitable plasticizers include sulfonamides, preferably aromatic sulfonamides such as benzenesulfonamides and toluenesulfonamides.
• Suitable sulfonamides include N-alkyl benzenesulfonamides and toluenesufonamides, such as N-butylbenzenesulfonamide, N-(2-hydroxypropyl)benzenesulfonamide, N-ethyl-o-toluenesulfonamide, N-ethyl-p-toluenesulfonamide, o-toluenesulfonamide, p-toluenesulfonamide, and the like.
• Preferred are N-butylbenzenesulfonamide, N-ethyl-o-toluenesulfonamide, and N-ethyl-p-toluenesulfonamide.
• the plasticizer may be incorporated into the composition by melt-blending the polymer with plasticizer and, optionally, other ingredients, or during polymerization. If the plasticizer is incorporated during polymerization, the polyamide monomers are blended with one or more plasticizers prior to starting the polymerization cycle and the blend is introduced to the polymerization reactor. Alternatively, the plasticizer can be added to the reactor during the polymerization cycle.
• the polyamide composition contains no more than 5 weight percent of plasticizer.
• thermoplastic composition is a mixture by melt-blending, in which all polymeric ingredients are adequately mixed, and all non-polymeric ingredients are adequately dispersed in a polymer matrix.
• Any melt-blending method may be used for mixing polymeric ingredients and non-polymeric ingredients of the present invention.
• polymeric ingredients and non-polymeric ingredients may be fed into a melt mixer, such as single screw extruder or twin screw extruder, agitator, single screw or twin screw kneader, or Banbury mixer, and the addition step may be addition of all ingredients at once or gradual addition in batches.
• thermoplastic composition having a polyhydric alcohol having two or more hydroxyl groups is useful in increasing long-term thermal stability at high temperatures of molded or extruded articles made therefrom.
• the long-term thermal stability of the articles can be assessed by air oven ageing (AOA) of 4 mm thick test samples at various test temperatures for various test periods of time.
• the test temperature for the composition disclosed herein is at 150° C. and for about 1000 hours test period.
• the term “at 150° C.” refers to the nominal temperature of the environment to which the test bars are exposed; with the understanding that the actual temperature may vary by ⁇ 2° C. from the nominal test temperature.
• test samples after air oven ageing, are tested for tensile strength and strain at break, according to ISO 527-2/1A test method; and compared with a control aged at said test temperature for 72 hours. Ageing the control at the test temperature for 72 hours may allow crystallization to equilibrate in the molded test specimens, and thus may allow more reliable measure of AOA performance. The comparison with the controls provides the retention of strain at break, and thus the various compositions can be assessed as to long-term high temperature ageing performance.
• the molded 4 mm test specimens of polyamide composition as disclosed herein, have a retention of strain at break of at least 80% after AOA at 150° C. for 1000 hours and preferably at least 90%, based upon comparison with controls exposed at said test temperature for 72 hours.
• the molded 4 mm test specimens of polyamide composition as disclosed herein, have a retention of strain at break of at least 50% after AOA at 150° C. for about 2000 hours and preferably at least 75%, based upon comparison with controls exposed at said test temperature for 72 hours
• the present invention relates a use of the above disclosed thermoplastic compositions for high temperature applications.
• the present invention relates to a method for manufacturing an article by shaping the thermoplastic composition of the invention.
• articles are films or laminates, automotive parts or engine parts or electrical/electronics parts.
• shaping it is meant any shaping technique, such as for example extrusion, injection moulding, thermoform moulding, compression moulding or blow moulding.
• the article is shaped by injection moulding or blow moulding.
• the molded or extruded thermoplastic articles disclosed herein may have application in automotive and other components that meet one or more of the following requirements: high chemical resistance to polar chemicals such as such as zinc chloride and calcium chloride, high impact requirements; resistance to high temperature; resistance to oil and fuel environment; resistance to chemical agents such as coolants; low permeability to fuels and gases, e.g. carbon dioxide.
• Specific extruded or molded thermoplastic articles are selected from the group consisting of pipes for transporting liquids and gases, inner linings for pipes, fuel lines, air break tubes, coolant pipes, air ducts, pneumatic tubes, hydraulic houses, cable covers, cable ties, connectors, canisters, and push-pull cables.
• Examples 1-3 and comparative examples C-1-C-3 were prepared by melt blending the ingredients listed in the Table in a Buss 55 mm extruder, operating at about 230° C. for PA1010 compositions and 250° C. for PA612 compositions, using a screw speed of about 180 rpm, and a throughput of 100 kg/hour. Ingredient quantities shown in the Table are given in weight percent on the basis of the total weight of the thermoplastic composition.
• the compounded mixture was extruded in the form of laces or strands, cooled in a water bath, chopped into granules and placed into sealed aluminum lined bags in order to prevent moisture pick up.
• the cooling and cutting conditions were adjusted to ensure that the materials were kept below 0.15 wt % of moisture level.
• the thickness of the test specimens was 4 mm and a width of 10 mm according to ISO 527/1A at a testing speed of 50 mm/min (tensile strength and elongation). Tensile Modulus was measured at 50 mm/min.
• test specimens were heat aged in a re-circulating air ovens (Heraeus type UT6060) according to the procedure detailed in ISO 2578. At various heat aging times, the test specimens were removed from the oven, allowed to cool to room temperature and sealed into aluminum lined bags until ready for testing. The tensile mechanical properties were then measured according to ISO 527 using a Zwick tensile instrument. The average values obtained from 5 specimens are given in the Table.
• Retention of strain at break corresponds to the percentage of the strain at break at 1008 hours and 2328 hours heat ageing in comparison with the value of specimens after heat aging for 72 hours considered as being 100%.
• PA612 is Zytel® 158 NC010 resin, having a melting point of about 218° C., available from E. I. du Pont de Nemours and Company, Wilmington, Del.
• PA1010 is Herox® polyamide resin available from E. I. du Pont de Nemours and Company, Wilmington, Del.
• Surlyn®9320 copolymer refers to an ethylene/methacrylic acid copolymer, zinc neutralized, available from E.I. DuPont de Nemours and Company, Wilmington, Del., USA.
• Elvaloy EP4934-4 refers to an ethylene/glycidyl methacrylate copolymer available from E.I. DuPont de Nemours and Company, Wilmington, Del., USA.
• Colloids PE 48/93 refers to a carbon black dispersed in polyethylene available from Colloids Limited.
• DPE refers to dipentaerythritol that was from Perstorp Speciality Chemicals AB, Perstorp, Sweden as Di-Penta 93.
• Cu heat stabilizer refers to a mixture of 7 parts of potassium iodide and 1 part of copper iodide in 0.5 part of a stearate wax binder.
• Irgafos® 168 stabilizer is a heat stabilizer available Ciba Speciality Chemicals Inc, Switzerland.
• Irganox® 1098 stabilizer was available from Ciba Speciality Chemicals Inc, Switzerland.
• Chimassorb® 944 refers to (poly[[6-[(1,1,3,3-tetramethylbutyl)amino]-1,3,5-triazine-2,4-diyl][(2,2,6,6-tetramethyl-4-piperidinyl)-imino]-1,6-hexanediyl[(2,2,6,6-tetramethyl-4-piperidinyl)imino]]), supplied by Ciba Specialty Chemicals.
• Tinuvin® 234 refers to a HALS available from Ciba Specialty Chemicals.
• Unreinforced PA 612 compositions of Examples 3 with DPE and Comparative Example C-3 without DPE are listed in Table 1.
• Tensile properties after AOA at 150° C. at 72 h, 1008 h, and 2328 h, and % retention of strain at break are listed in Table 1.
• the example showed greater than 80% retention of strain at break, after 1008 hours AOA at 150° C., as compared to the 72 h AOA control. These results are significantly better than the comparative examples having no DPE present.

Landscapes

• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Proteomics, Peptides & Aminoacids (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Polyamides (AREA)
• Manufacture Of Macromolecular Shaped Articles (AREA)
• Rigid Pipes And Flexible Pipes (AREA)
• Extrusion Moulding Of Plastics Or The Like (AREA)

Priority Applications (1)

Applications Claiming Priority (2)

Publications (1)

Family

ID=41095667

Family Applications (10)

Family Applications Before (1)

Family Applications After (8)

Country Status (7)

Cited By (23)

Families Citing this family (106)

Citations (3)

Family Cites Families (57)

• 2009
  • 2009-07-30 CN CN2009801299732A patent/CN102112527B/zh not_active Expired - Fee Related
  • 2009-07-30 US US12/512,109 patent/US20100029819A1/en not_active Abandoned
  • 2009-07-30 US US12/512,195 patent/US20100028580A1/en not_active Abandoned
  • 2009-07-30 WO PCT/US2009/052238 patent/WO2010014801A1/en active Application Filing
  • 2009-07-30 WO PCT/US2009/052231 patent/WO2010014795A1/en active Application Filing
  • 2009-07-30 US US12/512,311 patent/US8445575B2/en not_active Expired - Fee Related
  • 2009-07-30 WO PCT/US2009/052217 patent/WO2010014790A1/en active Application Filing
  • 2009-07-30 CA CA2725384A patent/CA2725384A1/en not_active Abandoned
  • 2009-07-30 WO PCT/US2009/052219 patent/WO2010014791A1/en active Application Filing
  • 2009-07-30 EP EP09790987A patent/EP2307502A1/en not_active Withdrawn
  • 2009-07-30 WO PCT/US2009/052232 patent/WO2010014796A2/en active Application Filing
  • 2009-07-30 KR KR1020117004405A patent/KR101644200B1/ko active IP Right Review Request
  • 2009-07-30 CN CN2009801298212A patent/CN102112551B/zh not_active Expired - Fee Related
  • 2009-07-30 EP EP09790988A patent/EP2307503A1/en not_active Withdrawn
  • 2009-07-30 JP JP2011521315A patent/JP2011529990A/ja active Pending
  • 2009-07-30 JP JP2011521311A patent/JP2011529987A/ja not_active Withdrawn
  • 2009-07-30 WO PCT/US2009/052253 patent/WO2010014810A1/en active Application Filing
  • 2009-07-30 US US12/512,125 patent/US8445574B2/en not_active Expired - Fee Related
  • 2009-07-30 CN CN2009801298227A patent/CN102112526B/zh active Active
  • 2009-07-30 US US12/512,062 patent/US20100029837A1/en not_active Abandoned
  • 2009-07-30 CN CN2009801298157A patent/CN102112525B/zh active Active
  • 2009-07-30 CN CN2009801297737A patent/CN102112549B/zh not_active Expired - Fee Related
  • 2009-07-30 CA CA2726010A patent/CA2726010A1/en not_active Abandoned
  • 2009-07-30 CN CN2009801299747A patent/CN102112545A/zh active Pending
  • 2009-07-30 EP EP09803583.5A patent/EP2307499A4/en not_active Withdrawn
  • 2009-07-30 JP JP2011521317A patent/JP6042064B2/ja active Active
  • 2009-07-30 US US12/512,101 patent/US20100029820A1/en not_active Abandoned
  • 2009-07-30 CN CN2009801297741A patent/CN102112550A/zh active Pending
  • 2009-07-30 EP EP09790992.3A patent/EP2307504B1/en not_active Not-in-force
  • 2009-07-30 EP EP09791004.6A patent/EP2307482B1/en active Active
  • 2009-07-30 EP EP09790983.2A patent/EP2307480B1/en not_active Not-in-force
  • 2009-07-30 JP JP2011521314A patent/JP5677953B2/ja not_active Expired - Fee Related
  • 2009-07-30 KR KR1020117004583A patent/KR20110032001A/ko not_active Application Discontinuation
  • 2009-07-30 WO PCT/US2009/052212 patent/WO2010014785A1/en active Application Filing
  • 2009-07-30 EP EP20090790995 patent/EP2307481A1/en not_active Withdrawn
  • 2009-07-30 US US12/512,172 patent/US20100029821A1/en not_active Abandoned
  • 2009-07-30 JP JP2011521310A patent/JP5475777B2/ja not_active Expired - Fee Related
  • 2009-07-30 JP JP2011521324A patent/JP2011529993A/ja active Pending
  • 2009-07-30 JP JP2011521312A patent/JP5667054B2/ja not_active Expired - Fee Related
• 2012
  • 2012-04-26 US US13/456,517 patent/US20120208954A1/en not_active Abandoned
  • 2012-09-14 US US13/615,967 patent/US20130072608A1/en not_active Abandoned
  • 2012-10-04 US US13/644,536 patent/US20130053483A1/en not_active Abandoned

Patent Citations (3)

Also Published As

Similar Documents

Legal Events