WO2000034376A1 - Nanocomposite polymere argile comprenant un melange d'argile et procede de production - Google Patents

Nanocomposite polymere argile comprenant un melange d'argile et procede de production Download PDF

Info

Publication number
WO2000034376A1
WO2000034376A1 PCT/US1999/028988 US9928988W WO0034376A1 WO 2000034376 A1 WO2000034376 A1 WO 2000034376A1 US 9928988 W US9928988 W US 9928988W WO 0034376 A1 WO0034376 A1 WO 0034376A1
Authority
WO
WIPO (PCT)
Prior art keywords
ammonium
nanocomposite
mixture
octadecyl
intercalate
Prior art date
Application number
PCT/US1999/028988
Other languages
English (en)
Other versions
WO2000034376A8 (fr
Inventor
Robert Boyd Barbee
John Walker Gilmer
James Christopher Matayabas, Jr.
Tie Lan
Vasiliki Psihogios
Original Assignee
Eastman Chemical Company
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from PCT/US1999/028340 external-priority patent/WO2000034375A1/fr
Application filed by Eastman Chemical Company filed Critical Eastman Chemical Company
Priority to BR9916044-7A priority Critical patent/BR9916044A/pt
Priority to JP2000586817A priority patent/JP2003525964A/ja
Priority to EP99966036A priority patent/EP1137706A1/fr
Priority to MXPA01005694A priority patent/MXPA01005694A/es
Priority to AU21681/00A priority patent/AU771071B2/en
Publication of WO2000034376A1 publication Critical patent/WO2000034376A1/fr
Publication of WO2000034376A8 publication Critical patent/WO2000034376A8/fr

Links

Classifications

    • 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
    • C08K9/00—Use of pretreated ingredients
    • C08K9/04—Ingredients treated with organic substances
    • 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
    • C08K3/34—Silicon-containing compounds
    • C08K3/346—Clay
    • 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
    • C08K7/00—Use of ingredients characterised by shape
    • 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
    • C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K

Definitions

  • This invention relates generally to a polymer-clay nanocomposite comprising a mixture of clay materials. This invention further relates to articles produced from a nanocomposite, and a process for preparing a nanocomposite.
  • the clay-based polymer nanocomposites there is much interest in layered, clay-based polymer nanocomposites because of the improved properties exhibited by the nanocomposites. It is desirable to maximize delamination of the clay into individual platelet particles in order to maximize some property improvements, including barrier improvements, and to minimize deleterious effects on some properties including elongation-at-break. Ideally, the clay is exfoliated into particles with size less than about 100 nm in order to achieve clarity that is comparable to the clay- free polymer. To date, the only polymer/clay nanocomposites that meet this expectation are prepared by incorporation of organically treated clays during synthesis of the polymer from monomer.
  • Polyesters such as poly(ethylene terephthalate) (PET) are widely used in bottles and containers which are used for carbonated beverages, fruit juices, and certain foods.
  • Useful polyesters have high molecular weight values (high inherent viscosities (IN.s)) as determined by solution viscometry, which allow polyesters to be formed into parisons and subsequently molded into containers.
  • PET containers are not generally used for products requiring long shelf life. For example, oxygen transmission into PET bottles which contain beer, wine and certain food products causes these products to spoil.
  • multilayer structures comprising one or more barrier layers and one or more structural layers of PET.
  • multilayer structures have not found wide use and are not suitable for use as a container for beer due to the high cost, the large thickness of the barrier layer required and poor adhesion of the barrier layer with the structural layer.
  • U.S. Patent 4,739,007 discloses the preparation of ⁇ ylon-6/clay nanocomposites from caprolactam and alkyl ammonium-treated montmorillonite.
  • U.S. Patent 4,889,885 describes the polymerization of various vinyl monomers such as methyl methacrylate and isoprene in the presence of sodium montmorillonite.
  • Some patents describe the blending of up to 60 weight percent of intercalated clay materials with a wide range of polymers including polyamides, polyesters, polyurethanes, polycarbonates, polyolefms, vinyl polymers, thermosetting resins and the like. Such high loadings with modified clays are impractical and useless with most polymers because the melt viscosity of the blends increases so much that they cannot be molded.
  • WO 93/04117 discloses a wide range of polymers melt blended with up to 60 weight percent of dispersed platelet particles.
  • WO 93/04118 discloses nanocomposite materials of a melt processable polymer and up to 60 weight percent of a clay that is intercalated with organic onium salts. The use of a mixture of swellable layered clays or a clay mixture intercalated with an onium ion is not contemplated nor disclosed.
  • U.S. Patent 5,552,469 describes the preparation of intercalates derived from certain clays and water soluble polymers such as polyvinyl pyrrolidone, polyvinyl alcohol, and polyacrylic acid. The use of clay mixtures or mixtures intercalated with onium ions is specifically excluded.
  • JP Kokai patent no. 9-176461 discloses polyester bottles wherein the polyester contains unmodified sodium montmorillonite. Incorporation of the clay into the polyester by melt compounding is disclosed; however the use of clay mixtures or clays intercalated with onium ions was neither contemplated nor disclosed.
  • This invention provides a novel polymer nanocomposite comprising a mixture of clay materials. This invention also provides articles produced from this polymer nanocomposite that have improved properties.
  • a mixture of clays is useful for the preparation of a polymer/clay nanocomposite with sufficient exfoliation for improved properties and clarity for commercial applications, including film, bottles, and containers.
  • the polymer nanocomposite materials of this invention are useful for forming articles or packages that have improved gas barrier properties over neat PET, for example.
  • Containers made from these polymer composite materials are ideally suited for protecting consumable products, such as foodstuffs, soft drinks, and medicines.
  • This invention also seeks to provide a cost-effective method for producing nanocomposite compositions, and articles made therefrom, having sufficient barrier and clarity for wide spread applications as multilayer bottles and containers, including beer bottles.
  • the polymer/clay nanocomposite composition and process of this invention are especially suited for use in applications requiring crystalline, molded or thermoformed parts.
  • this invention in one embodiment, relates to a polymer-clay nanocomposite comprising (i) a melt-processible matrix polymer, and incorporated therein (ii) a mixture of at least two swellable layered clay materials.
  • this invention relates to a process for preparing a polymer-clay nanocomposite comprising (i) preparing a mixture of at least two swellable layered clay materials, and (ii) incorporating the mixture with a matrix polymer by melt processing the matrix polymer with the mixture.
  • “Clay material, "layered clay” or “layered clay material” shall mean any organic or inorganic material or mixtures thereof, such as a smectite clay mineral, which is in the form of a plurality of adjacent, bound layers.
  • the layered clay comprises platelet particles and is typically swellable.
  • Plate particles shall mean individual or aggregate unbound layers of the layered clay material. These layers may be in the form of individual platelet particles, ordered or disordered small aggregates of platelet particles (tactoids), and small aggregates of tactoids.
  • Dispersion or “dispersed” is a general term that refers to a variety of levels or degrees of separation of the platelet particles. The higher levels of dispersion include, but are not limited to, “intercalated” and “exfoliated.”
  • Intercalated or “intercalate” shall mean a layered clay material that includes an intercalant disposed between adjacent platelet particles or tactoids of the layered material to increase the interlay er spacing between the adjacent platelets and tactoids.
  • the intercalant is preferably an organic cation and may also be a matrix polymer.
  • Exfoliate or “exfoliated” shall mean platelets dispersed predominantly in an individual state throughout a carrier material, such as a matrix polymer. Typically, “exfoliated” is used to denote the highest degree of separation of platelet particles.
  • Exfoliation shall mean a process for forming an exfoliate from an intercalated or otherwise less dispersed state of separation.
  • Nanocomposite(s) or “nanocomposite composition(s)” shall mean a polymer or copolymer having dispersed therein a plurality of individual platelets obtained from an exfoliated, layered clay material.
  • Microx polymer shall mean a thermoplastic or melt-processible polymer in which the platelet particles are dispersed to form a nanocomposite.
  • the platelet particles are predominantly exfoliated in the matrix polymer to form a nanocomposite.
  • the present invention relates to clay mixtures, polymer/clay nanocomposite compositions comprising clay mixtures, a process for preparing a polymer/clay nanocomposite, and to molded articles, films, fiber, etc. prepared from the polymer/clay nanocomposites of this invention.
  • the process of this invention may be used to prepare a wide variety of polymer/clay nanocomposite compositions, the most preferred being polyester/clay nanocomposites.
  • the degree of improved gas barrier depends upon the embodiment ratio of the resulting particle platelets and aggregates, the degree to which they are dispersed or uniformly distributed, and the degree to which they are ordered perpendicular to the flux of the permeant.
  • the platelet particles representative of the bulk of the composite be exfoliated, and preferably be highly exfoliated, in the matrix polymer such that the majority, preferably at least about 75 percent and perhaps as much as at least about 90 percent or more of the platelet particles, be dispersed in the form of individual platelets and small aggregates having a thickness in the shortest dimension of less than about 20 nm and preferably less than about 10 nm, as estimated from TEM images.
  • Polymer-platelet nanocomposites containing more individual platelets and fewer aggregates, ordered or disordered, are most preferred.
  • the prior art has defined the degree of separation of platelet particles based on peak intensity and basal spacing value, or lack of predominant basal spacing, as determined by X-ray analyses of polymer-platelet composites. Even though X-ray analysis alone often does not unambiguously predict whether the platelet particles are individually dispersed in the polymer, it can often allow quantification of the level of dispersion achieved. Basal spacing by X-ray diffraction indicates the separation distance of a platelet in a tactoid rather than single platelets. X-ray diffraction intensity (basal spacing peak height) may correlate to barrier in an article resulting from a nanocomposite including a clay material mixture as described above.
  • a low basal spacing peak height indicates few tactoids; therefore, the remainder must be either individual platelets or tactoids that are disordered.
  • one organoclay a clay treated with an organic cation
  • another organoclay that has a low basal spacing, as shown by X-ray
  • two individual X-ray spacings are expected.
  • TEM images of polymer-platelet composites show that platelet particles which are incorporated into at least one polymer exist in a variety of forms, including, but not limited to, individual platelets (the exfoliated state), disordered agglomerates of platelets, well ordered or stacked aggregates of platelets (tactoids), swollen aggregates of stacked platelets (intercalated tactoids), and aggregates of tactoids. It has been discovered that intimately mixing two individual clays, for example, does not produce the expected two individual X-ray spacings.
  • Intimate mixing of a clay blend can be achieved by delaminating the stacked silicate layered structure of each clay or organoclay, usually from a solvent.
  • the clay (silicate) layers may be recombined upon removal of the solvent to provide a uniform dispersion of silicate layers within the clay blend.
  • Solvents useful for obtaining an intimate mixture of clays include, but are not limited to water, alcohols (e.g., methanol), chlorinated solvents (e.g., methylene chloride), ketones (e.g., acetone), esters (e.g., ethyl acetate), and/or ethers (e.g., tetrahydrofuran or dioxane). After intimately mixing the clays, the solvents are removed, and as such, low boiling point solvents are preferred.
  • alcohols e.g., methanol
  • chlorinated solvents e.g., methylene chloride
  • ketones e.g., acetone
  • esters e.g., ethyl acetate
  • ethers e.g., tetrahydrofuran or dioxane
  • the polymer/clay nanocomposites of this invention exhibit an unexpectedly lower gas permeability, particularly oxygen permeability, than clay-free polymers.
  • the present invention it has been found that using a mixture of layered clay materials while melt processing with a polymer gives a good dispersion of platelet particles in a resulting nanocomposite, creating mostly individual platelet particles.
  • the resulting nanocomposite has improved barrier to gas when formed into a wall or article compared to a neat polymer formed into the same or similar structure.
  • this invention relates to a polymer nanocomposite comprising a melt-processible polymer and up to about 25 weight percent of a mixture of swellable layered clay materials, which may be intercalated with an organic cation, preferably an onium ion.
  • the intercalated clay material mixture has platelet particles, which are dispersed in the polymer.
  • the polymer nanocomposite is preferably a polyester polymer or copolymer nanocomposite having an IN. of at least 0.5 dL/g as measured in 60 wt.%/40 wt.% phenol tetrachloroethane at 25°C.
  • a process for manufacturing the polymer nanocomposite of this invention comprises (1) preparing the layered clay material mixture and (2) incorporating the layered clay material mixture with a polymer by melt processing the polymer and the layered clay material mixture.
  • Melt processing includes melt and extrusion compounding.
  • Use of extrusion compounding to mix the clay mixture and the polymer presents advantages. Chiefly, the extruder is able to handle the high viscosity exhibited by the nanocomposite material.
  • the use of solvents can be avoided. Low molecular weight liquids can often be costly to remove from the nanocomposite resin.
  • the nanocomposite composition of the present invention comprises less than about 25 weight percent, preferably from about 0.5 to about 20 weight percent, more preferably from about 0.5 to about 15 weight percent, and most preferably from about 0.5 to about 10 weight percent of clay mixtures.
  • the amount of platelet particles is determined by measuring the amount of silicate residue in the ash of the polymer/platelet composition when treated in accordance with ASTM D5630-94.
  • Useful clay materials include natural, synthetic, and modified phyllo silicates.
  • Natural clays include smectite clays, such as montmorillonite, hectorite, mica, vermiculite, bentonite, nontronite, beidellite, volkonskoite, saponite, magadite, kenyaite, and the like.
  • Synthetic clays include synthetic mica, synthetic saponite, synthetic hectorite, and the like.
  • Modified clays include fluoronated montmorillonite, fluoronated mica, and the like. Suitable clays are available from various companies including Nanocor, Inc., Southern Clay Products, Kunimine Industries, Ltd., and Rheox.
  • the layered clay materials useful in this invention are an agglomeration of individual platelet particles that are closely stacked together like cards, in domains called tactoids.
  • the individual platelet particles of the clays preferably have thickness of less than about 2 nm and diameter in the range of about 10 to about 3000 nm.
  • the clays are dispersed in the polymer so that most of the clay material exists as individual platelet particles, small tactoids, and small aggregates of tactoids.
  • a majority of the tactoids and aggregates in the polymer/clay nanocomposites of the present invention will have thickness in its smallest dimension of less than about 20 nm. Polymer/clay nanocomposite compositions with the higher concentration of individual platelet particles and fewer tactoids or aggregates are preferred.
  • the layered clay materials are typically swellable free flowing powders having a cation exchange capacity from about 0.3 to about 3.0 milliequivalents per gram of mineral (meq/g), preferably from about 0.9 to about 1.5 meq/g.
  • the clay may have a wide variety of exchangeable cations present in the galleries between the layers of the clay, including, but not limited to, cations comprising the alkaline metals (group IA), the alkaline earth metals (group IIA), and their mixtures.
  • the most preferred cation is sodium; however, any cation or combination of cations may be used provided that most of the cations may be exchanged for organic cations (onium ions).
  • the exchange may occur by treating a individual clay for a mixture or a mixture of clays with organic cations.
  • Preferred clay materials for at least one of the components of the clay mixture, are phyllosilicates of the 2:1 type having a cation exchange capacity of
  • the most preferred clay materials, for at least one of the components of the clay mixture, are smectite clay minerals, particularly bentonite or montmorillonite, more particularly Wyoming-type sodium montmorillonite or Wyoming-type sodium bentonite.
  • preferred clay mixtures include mixtures in which at least one the clay components has an alkyl group containing at least 12 carbon atoms and the other clay component has an alkyl group containing less than 12 carbon atoms.
  • Preferred mixtures would be a mixture of dodecyl ammonium montmorillonite with tetramethyl ammonium montmorillonite or dodecyl ammonium montmorillonite with sodium montmorillonite.
  • the most preferred mixtures include mixtures in which at least one clay component has an alkyl group containing 18 carbons and the other component has an alkyl group containing less than 18 carbons.
  • Most preferred mixtures would be mixtures of bis(2-hydroxyethyl) octadecyl methyl ammonium montmorillonite with dodecyl ammonium montmorillonite and octadecyl trimefhyl ammonium montmorillonite with tetramethyl ammonium montmorillonite.
  • the preferred ratios of the clay mixtures include any ratio from about 75/25 to about 25/75, and more preferably from about 60/40 to about
  • Non-clay materials having the above-described ion-exchange capacity and size such as chalcogens, may also be used as a source of platelet particles under the present invention.
  • Chalcogens are salts of a heavy metal and group VIA (O, S, Se, and Te). These materials are known in the art and do not need to be described in detail here.
  • the clay mixtures of this invention may comprise refined but unmodified clays, modified clays or mixtures of modified and unmodified clays.
  • Many clay treatments used to modify the clay for the purpose of improving dispersion of clay materials are known and may be used in the practice of this invention. The clay treatments may be conducted prior to, during, or after mixing the clay materials. When the treatments are made prior to mixing, the modifications may be the same or different.
  • an intercalated layered clay material mixture is prepared by the reaction of a swellable layered clay with an organic cation, preferably an ammonium compound (to effect partial or complete cation exchange). If desired, two or more organic cations may be used to treat a clay. Moreover, mixtures of organic cations may also be used to prepare an intercalated layered clay material, wherein the intercalated layered clay material in a polymer nanocomposite comprises a mixture of intercalated clays. The process to prepare the organoclays (intercalated clays) may be conducted in a batch, semi-batch, or continuous manner.
  • Organic cations used to intercalate a clay material or a mixture of clay materials of a nanocomposite of this invention are derived from organic cation salts, preferably onium salt compounds.
  • Organic cation salts useful for the nanocomposite and process of this invention may generally be represented by the following formula (I):
  • Rt (I) wherein M is either nitrogen or phosphorous; X " is a halide, hydroxide, or acetate anion, preferably chloride and bromide; and Ri, R , R 3 , and R are independently organic and/or oligomeric ligands or may be hydrogen.
  • useful organic ligands include, but are not limited to, linear or branched alkyl groups having 1 to 22 carbon atoms, aralkyl groups which are benzyl and substituted benzyl moieties including fused-ring moieties having linear chains or branches of 1 to 100 carbon atoms in the alkyl portion of the structure, aryl groups such as phenyl and substituted phenyl including fused- ring aromatic substituents, beta, gamma unsaturated groups having six or less carbon atoms, and alkyleneoxide groups having repeating units comprising 2 to 6 carbon atoms.
  • useful oligomeric ligands include, but are not limited to, poly(alkylene oxide), polystyrene, polyacrylate, polycaprolactone, and the like.
  • Examples of useful organic cations include, but are not limited to, alkyl ammonium ions, such as tetramethyl ammonium, hexyl ammonium, butyl ammonium, bis(2-hydroxyethyl) dimethyl ammonium, hexyl benzyl dimethyl ammonium, benzyl trimefhyl ammonium, butyl benzyl dimethyl ammonium, tetrabutyl ammonium, di(2-hydroxyethyl) ammonium, and the like, and alkyl phosphonium ions such as tetrabutyl phosphonium, trioctyl octadecyl phosphonium, tetraoctyl phosphonium, octadecyl triphenyl phosphonium, and the like or mixtures thereof.
  • alkyl ammonium ions such as tetramethyl ammonium, hexyl ammonium, butyl ammoni
  • organic cations for this invention include, but are not limited to, alkyl ammonium ions such as dodecyl ammonium, octadecyl trimethyl ammonium, bis(2-hydroxyethyl) octadecyl methyl ammonium, octadecyl benzyl dimethyl ammonium, and the like or mixtures thereof.
  • alkyl ammonium ions such as dodecyl ammonium, octadecyl trimethyl ammonium, bis(2-hydroxyethyl) octadecyl methyl ammonium, octadecyl benzyl dimethyl ammonium, and the like or mixtures thereof.
  • suitable polyalkoxylated ammonium compounds include the hydrochloride salts of polyalkoxylated amines such as JEFFAMLNE (of Huntsman Chemical), namely, JEFFAMLNE-506 and JEFFAMINE 505, and an amine available under the trade name ETHOMEEN (of Akzo Chemie America), namely, ETHOMEEN 18/25, which is octadecyl bis(polyoxyethylene[15])amine, wherein the numbers in brackets refer to the total number of ethylene oxide units.
  • JEFFAMLNE of Huntsman Chemical
  • ETHOMEEN of Akzo Chemie America
  • a further illustrative example of a suitable polyalkoxylated ammonium compound is ETHOQUAD 18/25 (of Akzo Chemie America), which is octadecyl methyl bis(polyoxyethylene[15]) ammonium chloride, wherein the numbers in brackets refer to the total number of ethylene oxide units.
  • the preferred organic cation for use in polyesters, such as polyethylene terephthalates, is a polyalkoxylated ammonium compound, preferably ETHOQUAD 18/25.
  • One embodiment of this invention is the modification of a layered clay with an organic cation salt by the process of dispersing a layered clay or mixture of clays into hot water, most preferably from 50 to 80°C, adding the organic cation salt separately or adding a mixture of the organic cation salts (neat or dissolved in water or alcohol) with agitation, then blending for a period of time sufficient for the organic cations to exchange most of the metal cations present in the galleries between the layers of the clay material(s). Then, the organically modified layered clay material(s) is isolated by methods known in the art including, but not limited to, filtration, centrifugation, spray drying, and their combinations.
  • organic cation salt(s) it is desirable to use a sufficient amount of the organic cation salt(s) to permit exchange of most of the metal cations in the galleries of the layered particle for the organic cation(s); therefore, at least about 0.5 equivalent of total organic cation salts is used and up to about 3 equivalents of organic cation salts can be used. It is preferred that about 0.5 to 2 equivalents of organic cation salts be used, more preferably about 0.9 to 1.5 equivalents. It is desirable, but not required, to remove most of the metal cation salts and most of the excess organic cation salts by washing and other techniques known in the art.
  • the particle size of the clay material Prior to incorporation into a polymer, the particle size of the clay material is reduced in size by methods known in the art, including, but not limited to, grinding, pulverizing, hammer milling, jet milling, and their combinations. It is preferred that the average particle size be reduced to less than 100 micron in diameter, more preferably less than 50 micron in diameter, and most preferably less than 20 micron in diameter.
  • the clay mixtures may be further treated for the purposes of aiding exfoliation in the composite and/or improving the strength of the polymer/clay interface. Any treatment that achieves the above goals may be used. Examples of useful treatments include intercalation with water-soluble or water-insoluble polymers, organic reagents or monomers, silane compounds, metals or organometallics, and/or their combinations. Treatment of the clay can be accomplished prior to the addition of a polymer to the clay material mixture, during the dispersion of the clay mixture with a polymer or during a subsequent melt blending or melt fabrication step. Examples of useful pretreatment with polymers and oligomers include those disclosed in U.S. Patents 5,552,469 and 5,578,672, incorporated herein by reference.
  • Examples of useful polymers for treating the clay mixtures include polyvinyl pyrrolidone, polyvinyl alcohol, polyethylene glycol, polytetrahydrofuran, polystyrene, polycaprolactone, certain water-dispersible polyesters, Nylon-6 and the like.
  • Examples of useful pretreatment with organic reagents and monomers include those disclosed in EP 780,340 Al, incorporated herein by reference.
  • Examples of useful organic reagents and monomers for intercalating the swellable layered clay include dodecylpynolidone, caprolactone, caprolactam, ethylene carbonate, ethylene glycol, bishydroxyethyl terephthalate, dimethyl terephthalate, and the like or mixtures thereof.
  • Examples of useful pretreatment with silane compounds include those treatments disclosed in WO 93/11190, incorporated herein by reference.
  • Examples of useful silane compounds includes (3- glycidoxypropyl)trimethoxysilane, 2-methoxy (polyethyleneoxy)propyl heptamethyl trisiloxane, octadecyl dimethyl (3-trimethoxysilylpropyl) ammonium chloride and the like.
  • a dispersing aid may be present during or prior to the formation of the composite by melt mixing for the purposes of aiding exfoliation of the treated or untreated swellable layered particles into the polymer.
  • Many such dispersing aids are known, covering a wide range of materials including water, alcohols, ketones, aldehydes, chlorinated solvents, hydrocarbon solvents, aromatic solvents, and the like or combinations thereof.
  • dispersing aids and/or pretreatment compounds may account for significant amount of the total composition, in some cases up to about 30 weight percent. While it is prefened to use as little dispersing aid/pretreatment compound as possible, the amounts of dispersing aids and/or pretreatment compounds may be as much as about 8 times the amount of the platelet particles.
  • melt-processible polymer or oligomer may be used in this invention.
  • melt-processible polymers are polyesters, polyetheresters, polyamides, polyesteramides, polyurethanes, polyimides, polyetherimides, polyureas, polyamideimides, polyphenyleneoxides, phenoxy resins, epoxy resins, polyolefms, polyacrylates, polystyrenes, polyethylene-co- vinyl alcohols (ENOH), and the like or their combinations and blends.
  • the prefened polymers are linear or nearly linear, polymers with other architectures, including branched, star, cross-linked and dendritic structures, may be used if desired.
  • the prefened polymers include those materials that are suitable for use in the formation of multilayer structures with polyesters, and include polyesters (such as poly(ethylene terephthalate)), polyamides (such as poly(m-xylylene adipamide)), polyethylene-co-vinyl alcohols (such as ENOH), and similar or related polymers and/or copolymers.
  • polyesters such as poly(ethylene terephthalate)
  • polyamides such as poly(m-xylylene adipamide)
  • polyethylene-co-vinyl alcohols such as ENOH
  • the most prefened polyester is poly(ethylene terephthalate) and/or its copolymers.
  • the most prefened polyamide is poly(m-xylylene adipamide) and/or its copolymers.
  • Suitable polyesters include at least one dibasic acid and at least one glycol.
  • the primary dibasic acids are terephthalic, isophthalic, naphthalenedicarboxylic, 1 ,4-cyclohexanedicarboxylic acid and the like.
  • the various isomers of naphthalenedicarboxylic acid or mixtures of isomers may be used, but the 1,4-, 1,5, 2,6-, and 2,7-isomers are prefened.
  • the 1 ,4- cyclohexanedicarboxylic acid may be in the form of cis, trans, or cis/trans mixtures.
  • the lower alkyl esters or acid chlorides may be also be used.
  • the prefened polyester is poly(ethylene terephthalate) (PET) or a copolymer thereof.
  • PET poly(ethylene terephthalate)
  • the polyester may be prepared from one or more of the following dicarboxylic acids and one or more of the
  • the dicarboxylic acid component of the polyester may optionally be modified with up to about 50 mole percent of one or more different dicarboxylic acids.
  • additional dicarboxylic acids include dicarboxylic acids having from 3 to about 40 carbon atoms, and more preferably dicarboxylic acids selected from aromatic dicarboxylic acids preferably having 8 to 14 carbon atoms, aliphatic dicarboxylic acids preferably having 4 to 12 carbon atoms, or cycloaliphatic dicarboxylic acids preferably having 8 to 12 carbon atoms.
  • dicarboxylic acids examples include phthalic acid, isophthalic acid, naphthalene- 2,6-dicarboxylic acid, cyclohexanedicarboxylic acid, cyclohexanediacetic acid, diphenyl-4,4'-dicarboxylic acid, phenylene (oxyacetic acid) succinic acid, glutaric acid, adipic acid, azelaic acid, sebacic acid, and the like. Polyesters may also be prepared from two or more of the above dicarboxylic acids.
  • Typical glycols used in the polyester include those containing from two to about ten carbon atoms.
  • Prefened glycols include ethylene glycol, propanediol, 1 ,4-butanediol, 1 ,6-hexanediol, 1 ,4-cyclohexanedimethanol, diethylene glycol and the like.
  • the glycol component may optionally be modified with up to about 50 mole percent, preferably up to about 25 mole percent, and more preferably up to about 15 mole percent of one or more different diols.
  • Such additional diols include cycloaliphatic diols preferably having 3 to 20 carbon atoms or aliphatic diols preferably having 3 to 20 carbon atoms.
  • diols examples include: diethylene glycol, triethylene glycol, 1,4-cyclohexanedimethanol, propane- 1, 3 -diol, butane- 1,4-diol, pentane-1,5- diol, hexane-l,6-diol, 3-methylpentanediol-(2,4), 2-methylpentanediol-(l,4),
  • Polyesters may also be prepared from two or more of the above diols.
  • Small amounts of multifunctional polyols such as trimethylolpropane, pentaerythritol, glycerol and the like may be used, if desired.
  • 1 ,4- cyclohexanedimethanol it may be the cis, trans or cis/trans mixtures.
  • phenylenedi(oxyacetic acid) it may be used as 1,2; 1,3; 1,4 isomers, or mixtures thereof.
  • the polymer may also contain small amounts of trifunctional or tetrafunctional comonomers to provide controlled branching in the polymers.
  • Such comonomers include trimellitic anhydride, trimethylolpropane, pyromellitic dianhydride, pentaerythritol, trimellitic acid, trimellitic acid, pyromellitic acid and other polyester forming polyacids or polyols generally known in the art.
  • Suitable polyamides include partially aromatic polyamides, aliphatic polyamides, wholly aromatic polyamides and/or mixtures thereof.
  • partially aromatic polyamide it is meant that the amide linkage of the partially aromatic polyamide contains at least one aromatic ring and a nonaromatic species.
  • Suitable polyamides have an article forming molecular weight and preferably an IN. of greater than 0.4.
  • Prefened wholly aromatic polyamides comprise in the molecule chain at least 70 mole% of structural units derived from m-xylylene diamine or a xylylene diamine mixture comprising m-xylylene diamine and up to 30% of p- xylylene diamine and an aliphatic dicarboxylic acid having 6 to 10 carbon atoms, which are further described in Japanese Patent Publications No. 1156/75, No. 5751/75, No. 5735/75 and No. 10196/75 and Japanese Patent Application Laid-Open Specification No. 29697/75.
  • the low molecular weight polyamides may also contain small amounts of trifunctional or tetrafunctional comonomers such as trimellitic anhydride, pyromellitic dianhydride, or other polyamide forming polyacids and polyamines known in the art.
  • Prefened partially aromatic polyamides include, but are not limited to poly(m-xylylene adipamide), poly(m-xylylene adipamide-co-isophthalamide), poly(hexamethylene isophthalamide), poly(hexamethylene isophfhalamide-co- terephthalamide), poly(hexamethylene adipamide-co-isophthalamide), poly(hexamethylene adipamide-co-terephthalamide), poly(hexamethylene isophthalamide-co-terephthalamide) and the like or mixtures thereof.
  • More prefened partially aromatic polyamides include poly(m-xylylene adipamide), poly(hexamefhylene isophthalamide-co-terephthalamide), poly(m-xylylene adipamide-co-isophthalamide), and/or mixtures thereof.
  • the most prefened partially aromatic polyamide is poly( -xylylene adipamide).
  • Preferred aliphatic polyamides include, but are not limited to poly(hexamethylene adipamide) and poly (caprolactam). The most preferred aliphatic polyamide is poly(hexamethylene adipamide). Partially aromatic polyamides are prefened over the aliphatic polyamides where good thermal properties are crucial.
  • Prefened aliphatic polyamides include, but are not limited to polycapramide (nylon 6), poly-aminoheptanoic acid (nylon 7), poly- aminonanoic acid (nylon 9), polyundecane-amide (nylon 11), polyaurylactam (nylon 12), poly(ethylene-adipamide) (nylon 2,6), poly(tetramethylene- adipamide) (nylon 4,6), poly(hexamethylene-adipamide) (nylon 6,6), poly(hexamethylene-sebacamide) (nylon 6,10), poly(hexamethylene- dodecamide) (nylon 6,12), poly(octamethylene-adipamide) (nylon 8,6), poly(decamethylene-adipamide) (nylon 10,6), poly(dodecamethylene- adipamide) (nylon 12,6) and poly(dodecamethylene-sebacamide) (nylon 12,8).
  • polycapramide nylon 6
  • the most prefened polyamides include poly(m-xylylene adipamide), polycapramide (nylon 6) and polyhexamethylene- adipamide (nylon 6,6).
  • Poly(m-xylylene adipamide) is a prefened polyamide due to its availability, high barrier, and processability.
  • the polyamides are generally prepared by processes that are well known in the art.
  • the polymers of the present invention may also include additives normally used in polymers.
  • additives normally used in polymers.
  • additives known in the art are colorants, pigments, carbon black, glass fibers, fillers, impact modifiers, antioxidants, stabilizers, flame retardants, reheat aids, crystallization aids, acetaldehyde reducing compounds, recycling release aids, oxygen scavengers, plasticizers, nucleators, mold release agents, compatibilizers, and the like, or their combinations.
  • This invention also relates to monolayer and multilayer articles prepared from the nanocomposite material of this invention, including, but not limited to, film, sheet, pipes, tubes, profiles, molded articles, preforms, stretch blow molded films and containers, injection blow molded containers, extrusion blow molded films and containers, thermoformed articles and the like.
  • the containers are preferably bottles.
  • the bottles and containers of this invention provide increased shelf storage life for contents, including beverages and food that are sensitive to the permeation of gases.
  • Articles, more preferably containers, of the present invention often display a gas transmission or permeability rate (oxygen, carbon dioxide, water vapor) of at least 10% lower (depending on clay concentration) than that of similar containers made from clay-free polymer, resulting in conespondingly longer product shelf life provided by the container. Desirable values for the sidewall modulus and tensile strength may also be maintained.
  • the articles may also be multilayered.
  • the multilayered articles have a nanocomposite material disposed intermediate to other layers, although the nanocomposite may also be one layer of a two-layered article.
  • the nanocomposite may form the food contact layer of the desired articles. In other embodiments it is prefened that the nanocomposite be in a layer other than the food contact layer.
  • the multilayer articles may also contain one or more layers of the nanocomposite composition of this invention and one or more layers of a structural polymer.
  • structural polymers may be used.
  • Illustrative of structural polymers are polyesters, polyetheresters, polyamides, polyesteramides, polyurethanes, polyimides, polyetherimides, polyureas, polyamideimides, polyphenyleneoxides, phenoxy resins, epoxy resins, polyolefins, polyacrylates, polystyrene, polyethylene-co-vinyl alcohols (EVOH), and the like or their combinations and blends.
  • the prefened structural polymers are polyesters, such as poly(ethylene terephthalate) and its copolymers.
  • the polymer-clay nanocomposite and the molded article or extruded sheet may be formed at the same time by co-injection molding or co-extruding.
  • Another embodiment of this invention is the combined use of silicate layers uniformly dispersed in the matrix of a high barrier thermoplastic together with the multilayer approach to packaging materials.
  • the high barrier material is often the most expensive component in multilayer packaging, a reduction in the amount of this material used can be quite beneficial.
  • the nanocomposite layer being sandwiched between two outer polymer layers, the surface roughness is often considerably less than for a monolayer nanocomposite material.
  • the level of haze is reduced.
  • This example illustrates a method for preparing a blend of organoclays fabricated from different clays but containing the same alkylammonium tether.
  • Sodium montmorillonite (7.50 grams, 7.12 milliequivalents) supplied by Southern Clay Products and reported to have a cation exchange capacity of 95 milliequivalents/100 grams and Laponite RD (2.5 grams, 1.37 milliequivalents) were mixed in 490 ml of water at 60°C in a Vitamix blender to form a 2% by weight slurry of clay in water.
  • Octadecyltrimethylammonium chloride (5.9 grams, 8.49 milliequivalents), commercially available as a 50% solution in isopropanol as ARQUAD 18/50, was dissolved in 25 ml of water then added to the Vitamix blender containing the clay suspension.
  • This example illustrates a method for blending two organoclays in solvents and the melt compounding of this blend into PET.
  • Octadecyl methyl di(2-hydroxyethyl)ammonium montmorillonite (20.7 grams) and dodecylamrnonium montmorillonite (19.2 grams) were suspended in 1000 ml of a solution of 85 wt % toluene and 15 wt % methanol. The mixture was thoroughly blended with an Ultra Tunax T50 blender. The solvent was evaporated from the mixture and the solid remaining was dried in an oven at 60°C for 24 hours. The product exhibited a basal spacing by X-ray diffraction of 1.5 nanometers.
  • the polyester composite had an inherent viscosity of 0.56 dl g and an ash content of 4.5 wt %.
  • the pellets are dried at 115°C in a vacuum oven for about 16 hours then compression molded into about 10 mil film by pressing the sample between layers of polyimide film at 285°C.
  • the oxygen permeability of the polyester/composite is then determined by conecting for the permeability of the polyimide film and converting to a one-mil basis using conventional calculations.
  • the oxygen permeability rate is 5.48 cc-mil/100 in 2 -24 hour- atmosphere.
  • a film of poly(ethylene terephthalate) molded under conditions similar to those used above has an oxygen permeability of 14.0 cc-mil/100 in 2 -24 hour- atmosphere.
  • This example illustrates a method for blending an organoclay and sodium montmorillonite in solvents and the melt compounding of this blend into PET.
  • Octadecyl methyl di(2-hydroxyethyl)ammonium montmorillonite 39.9 grams
  • sodium montmorillonite 20 grams
  • the mixture was thoroughly blended with an Ultra Tunax T50 blender.
  • the solvent was evaporated from the mixture and the solid remaining was dried in an oven at
  • the product exhibited a basal spacing by X-ray diffraction of 1.4 nanometers.
  • Polyethylene terephthalate (375 grams) (or PET 9921 of Eastman Chemical Company) was dry blended with the mixed clays (25 grams) described above and the blend dried in a vacuum oven at 110°C for 16 hours.
  • the blend was extruded on a Leistritz Micro- 18 double screw extruder at 275°C and 200 rpm.
  • the molten strand was quenched in chilled water and pelletized.
  • the polyester composite had an inherent viscosity of 0.57 dl/g and an ash content of 4.8 wt %.
  • the pellets are dried at 115°C in a vacuum oven for about 16 hours then compression molded into about 10 mil film by pressing the sample between layers of polyimide film at 285°C.
  • the oxygen permeability of the polyester/composite is then determined by conecting for the permeability of the polyimide film and converting to a one-mil basis using conventional calculations.
  • the oxygen permeability rate is 5.76 cc-mil/100 in 2 -24 hour- atmosphere.
  • This example illustrates a method for blending an organoclay and the synthetic clay Laponite RD in solvents and the melt compounding of this blend into PET.
  • Octadecyl methyl di(2-hydroxyethyl)ammonium montmorillonite 39.9 grams
  • Laponite RD (20 grams) were suspended in 1000 ml of a solution of 85 wt % toluene and 15 wt % methanol.
  • the mixture was thoroughly blended with an Ultra Tunax T50 blender.
  • the solvent was evaporated from the mixture and the solid remaining was dried in an oven at 60°C for 24 hours.
  • the product exhibited a basal spacing by X-ray diffraction of 1.4 nanometers.
  • Polyethylene terephthalate (375 grams) (or PET 9921 of Eastman Chemical Company) was dry blended with the mixed clays (25 grams) described above and the blend dried in a vacuum oven at 110°C for 16 hours.
  • the blend was extruded on a Leistritz Micro- 18 double screw extruder at 275°C and 200 rpm.
  • the molten strand was quenched in chilled water and pelletized.
  • the polyester composite had an inherent viscosity of 0.63 dl/g and an ash content of 4.1 wt %.
  • the pellets are dried at 115°C in a vacuum oven for about 16 hours then compression molded into about 10 mil film by pressing the sample between layers of polyimide film at 285°C.
  • the oxygen permeability of the polyester/composite is then determined by conecting for the permeability of the polyimide film and converting to a one-mil basis using conventional calculations.
  • the oxygen permeability rate is 5.52 cc-mil/100 in -24 hour- atmosphere.
  • Example 1 The procedure of Example 1 was repeated using different weight percent combinations of sodium montmorillonite and Laponite RD. Sodium montmorillonite and Laponite RD were also tested individually. The results are shown in Table 1.
  • Table 1 The resulting clay mixtures, as shown in Table 1 , display X-ray diffraction basal spacings that are intermediate between that of the two clays individually. Intermediate basal spacings indicate that intimate mixing was achieved in the mixture and also indicates a transformation of the order of the clay materials from two basal spacings to one intermediate basal spacing. In other words, the spacing of each individual organoclay has been disordered from one basal spacing order to another.
  • Nanocor, Inc. provides several kinds of Na- montmorillonite clays. These clays originate from different geographic locations. For example, one Na-montmorillonite is called Na-CWC, which has a cation exchange capacity of about 1.4 meq per gram. Another Na- montmorillonite, called Na-Belle Yellow (Na-BY), has a cation exchange capacity of 1.2 meq per gram. Na-CWC and Na-BY also have different particle sizes and particle size distributions. Na-CWC is white-like, but with tint color when dispersed into water. Na-BY has yellow color in dry and slurry form.
  • the ODA solution was mixed with the mixed clay slurry.
  • Onium ion-intercalated clay precipitated from the slurry upon mixing.
  • the treated clay was filtered, washed, and dried according to procedures stated in the early text.
  • X-ray diffraction XRD results of the ODA-CWC/BY (1 :1) and ODA-CWC, and ODA-BY clays are given in the following table.
  • the milled clay was compounded into PET to form a nanocomposite and the compounded nanocomposite showed improved color compared to the nanocomposite prepared from single CWC or BY clays.
  • the nanocomposite demonstrated improved O 2 barrier properties compared with the PET-9921 (of Eastman Chemical) resin and nanocomposites prepared from single clays.
  • the nanocomposites prepared from the mixed clays are suitable for use in PET contained applications, such as bottled water, beer and soft drinks, as well as for incorporation into all other polymers. Comparative Example 1
  • Equal portions of octadecyltrimethylammonium-intercalated sodium montmorillonite and octadecylammonium-intercalated Laponite RD were dry mixed (in contrast to intimately mixed) and then evaluated by X-ray diffraction, which showed two basal spacings of 1.86 nm and 1.34 nm. These spacings are about the same as that of the individual clay materials, indicating that the order within each of the clay tactoids is preserved.
  • the dry mixed clay mixture did not transform the order from two basal spacings to one intermediate basal spacing. This lack of order transformation may result in less dispersion when the clay mixture is intercalated with a matrix polymer to form a polymer-clay nanocomposite.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Dispersion Chemistry (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Laminated Bodies (AREA)
  • Containers Having Bodies Formed In One Piece (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

Cette invention a trait à un nanocomposite comprenant, (i), une matrice polymère pouvant être traitée à chaud et, incorporé à cette matrice, (ii), un mélange constitué d'au moins deux matériaux argileux stratifiés. Elle porte également sur des articles produits à l'aide de ce nanocomposite ainsi que sur un procédé de préparation du nanocomposite.
PCT/US1999/028988 1998-12-07 1999-12-07 Nanocomposite polymere argile comprenant un melange d'argile et procede de production WO2000034376A1 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
BR9916044-7A BR9916044A (pt) 1998-12-07 1999-12-07 Nanocompósito de polìmero-argila, artigo, processo para preparar um nanocompósito de polìmero-argila, intercalado, esfoliado, e, processo para preparar um intercalado
JP2000586817A JP2003525964A (ja) 1998-12-07 1999-12-07 クレイ混合物を含むポリマー／クレイナノ複合材料及びその製造方法
EP99966036A EP1137706A1 (fr) 1998-12-07 1999-12-07 Nanocomposite polymere argile comprenant un melange d'argile et procede de production
MXPA01005694A MXPA01005694A (es) 1998-12-07 1999-12-07 Manocompuesto arcilla/polimero que consta de una mezcla de arcilla y un proceso para elaborar el mismo.
AU21681/00A AU771071B2 (en) 1998-12-07 1999-12-07 A polymer/clay nanocomposite comprising a clay mixture and a process for making same

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US11107498P 1998-12-07 1998-12-07
US60/111,074 1998-12-07
USPCT/US99/28340 1999-11-30
PCT/US1999/028340 WO2000034375A1 (fr) 1998-12-07 1999-11-30 Nanocomposite a base de polymere/d'argile comprenant unelange d'argile et procede de fabrication correspondant

Publications (2)

Publication Number Publication Date
WO2000034376A1 true WO2000034376A1 (fr) 2000-06-15
WO2000034376A8 WO2000034376A8 (fr) 2000-10-19

Family

ID=26795917

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1999/028988 WO2000034376A1 (fr) 1998-12-07 1999-12-07 Nanocomposite polymere argile comprenant un melange d'argile et procede de production

Country Status (6)

Country Link
EP (1) EP1137706A1 (fr)
JP (1) JP2003525964A (fr)
AU (1) AU771071B2 (fr)
BR (1) BR9916044A (fr)
MX (1) MXPA01005694A (fr)
WO (1) WO2000034376A1 (fr)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002003609A (ja) * 2000-06-23 2002-01-09 Nippon Synthetic Chem Ind Co Ltd:The 樹脂組成物の製造法
JP2002003608A (ja) * 2000-06-23 2002-01-09 Nippon Synthetic Chem Ind Co Ltd:The 樹脂組成物の製造法
EP1286825A1 (fr) * 2000-05-12 2003-03-05 Pechiney Emballage Flexible Europe Contenants dotes de proprietes barriere et mecanique ameliorees
JP2003342432A (ja) * 2002-05-24 2003-12-03 Eastman Kodak Co ポリマーナノ複合材料
WO2004005388A1 (fr) * 2002-07-05 2004-01-15 Exxonmobil Chemical Patents Inc. Nanocomposite elastomere fonctionnalise
WO2004022651A2 (fr) * 2002-09-06 2004-03-18 Ems-Chemie Ag Procede de production de nanocomposites a base de polyamides et pieces moulees par injection pouvant etre produites a partir de ces nanocomposites
WO2006069131A1 (fr) * 2004-12-22 2006-06-29 E. I. Du Pont De Nemours And Company Nanocomposites de polyester/argile pour applications de barrieres
WO2007098784A1 (fr) * 2006-03-03 2007-09-07 Pirelli Tyre S.P.A. Pneu et composition élastomère réticulable
CN106867238A (zh) * 2015-12-14 2017-06-20 现代自动车株式会社 用于燃料填充管的聚酰胺复合树脂组合物
CN110036073A (zh) * 2016-11-01 2019-07-19 信一化学工业株式会社 具有优异的气体阻隔性的聚酰胺类复合树脂组合物

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6613021B2 (ja) * 2014-06-06 2019-11-27 積水化学工業株式会社 トップエミッション型有機エレクトロルミネッセンス表示素子封止用樹脂組成物、トップエミッション型有機エレクトロルミネッセンス表示素子封止用樹脂シート、及び、トップエミッション型有機エレクトロルミネッセンス表示素子
KR101986733B1 (ko) * 2018-01-03 2019-06-07 (주)대아씨앤아이 기체차단성 수지 조성물 및 이를 이용한 기체차단성 용기
KR102570403B1 (ko) * 2023-02-22 2023-08-28 순천향대학교 산학협력단 나노클레이-폴리우레탄 나노복합체 및 이의 용도

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996025458A1 (fr) * 1995-02-15 1996-08-22 Concrete Sealants, Inc. Compositions arretant l'eau et procedes pour les preparer
WO1997017398A1 (fr) * 1995-11-07 1997-05-15 Southern Clay Products, Inc. Compositions a base d'argile riche en matieres organiques permettant de gelifier des systemes de resine polyester non saturee
JPH09217012A (ja) * 1996-02-13 1997-08-19 Asahi Chem Ind Co Ltd 熱可塑性樹脂／層状粘土鉱物複合材料の製造方法
WO1998053000A1 (fr) * 1997-05-20 1998-11-26 Exxon Chemical Patents Inc. Nanocomposites de resine thermoplastique renforces en caoutchouc

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996025458A1 (fr) * 1995-02-15 1996-08-22 Concrete Sealants, Inc. Compositions arretant l'eau et procedes pour les preparer
WO1997017398A1 (fr) * 1995-11-07 1997-05-15 Southern Clay Products, Inc. Compositions a base d'argile riche en matieres organiques permettant de gelifier des systemes de resine polyester non saturee
JPH09217012A (ja) * 1996-02-13 1997-08-19 Asahi Chem Ind Co Ltd 熱可塑性樹脂／層状粘土鉱物複合材料の製造方法
WO1998053000A1 (fr) * 1997-05-20 1998-11-26 Exxon Chemical Patents Inc. Nanocomposites de resine thermoplastique renforces en caoutchouc

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Section Ch Week 199743, Derwent World Patents Index; Class A23, AN 1997-466289, XP002134181 *

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6841211B1 (en) 2000-05-12 2005-01-11 Pechiney Emballage Flexible Europe Containers having improved barrier and mechanical properties
EP1286825A1 (fr) * 2000-05-12 2003-03-05 Pechiney Emballage Flexible Europe Contenants dotes de proprietes barriere et mecanique ameliorees
EP1286825A4 (fr) * 2000-05-12 2004-06-09 Pechiney Emballage Flexible Eu Contenants dotes de proprietes barriere et mecanique ameliorees
JP2002003608A (ja) * 2000-06-23 2002-01-09 Nippon Synthetic Chem Ind Co Ltd:The 樹脂組成物の製造法
JP2002003609A (ja) * 2000-06-23 2002-01-09 Nippon Synthetic Chem Ind Co Ltd:The 樹脂組成物の製造法
JP2003342432A (ja) * 2002-05-24 2003-12-03 Eastman Kodak Co ポリマーナノ複合材料
WO2004005388A1 (fr) * 2002-07-05 2004-01-15 Exxonmobil Chemical Patents Inc. Nanocomposite elastomere fonctionnalise
US8399551B2 (en) 2002-07-05 2013-03-19 Exxonmobil Chemical Patents Inc. Functionalized elastomer nanocomposite
WO2004022651A3 (fr) * 2002-09-06 2004-05-06 Ems Chemie Ag Procede de production de nanocomposites a base de polyamides et pieces moulees par injection pouvant etre produites a partir de ces nanocomposites
WO2004022651A2 (fr) * 2002-09-06 2004-03-18 Ems-Chemie Ag Procede de production de nanocomposites a base de polyamides et pieces moulees par injection pouvant etre produites a partir de ces nanocomposites
WO2006069131A1 (fr) * 2004-12-22 2006-06-29 E. I. Du Pont De Nemours And Company Nanocomposites de polyester/argile pour applications de barrieres
WO2007098784A1 (fr) * 2006-03-03 2007-09-07 Pirelli Tyre S.P.A. Pneu et composition élastomère réticulable
CN106867238A (zh) * 2015-12-14 2017-06-20 现代自动车株式会社 用于燃料填充管的聚酰胺复合树脂组合物
CN110036073A (zh) * 2016-11-01 2019-07-19 信一化学工业株式会社 具有优异的气体阻隔性的聚酰胺类复合树脂组合物

Also Published As

Publication number Publication date
AU2168100A (en) 2000-06-26
JP2003525964A (ja) 2003-09-02
AU771071B2 (en) 2004-03-11
BR9916044A (pt) 2001-10-02
WO2000034376A8 (fr) 2000-10-19
MXPA01005694A (es) 2002-04-24
EP1137706A1 (fr) 2001-10-04

Similar Documents

Publication Publication Date Title
US6653388B1 (en) Polymer/clay nanocomposite comprising a clay mixture and a process for making same
US6387996B1 (en) Polymer/clay intercalates, exfoliates; and nanocomposites having improved gas permeability comprising a clay material with a mixture of two or more organic cations and a process for preparing same
US6486253B1 (en) Polymer/clay nanocomposite having improved gas barrier comprising a clay material with a mixture of two or more organic cations and a process for preparing same
EP1141136B1 (fr) Nanocomposite polymere/argile comportant un polymere ou un oligomere fonctionnalise et procede de production
US6552113B2 (en) Polymer-clay nanocomposite comprising an amorphous oligomer
US6828370B2 (en) Intercalates and exfoliates thereof having an improved level of extractable material
EP1155079B1 (fr) Nanocomposite a base de polymere/d'argile et procede de preparation correspondant
EP1144494B1 (fr) Nanocomposite a base de polyamide amorphe et d'argile impermeable et son procede de production
US20020137834A1 (en) Polymer/clay nanocomposite comprising a functionalized polymer or oligomer and a process for preparing same
AU771071B2 (en) A polymer/clay nanocomposite comprising a clay mixture and a process for making same
AU758250B2 (en) A polymer/clay nanocomposite having improved gas barrier comprising a clay material with a mixture of two or more organic cations and a process for preparing same
MXPA01005599A (es) Nanocompuestos de polimero/arcilla y proceos para hacerlo

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AU BR CA CN JP MX

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
AK Designated states

Kind code of ref document: C1

Designated state(s): AU BR CA CN JP MX

AL Designated countries for regional patents

Kind code of ref document: C1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE

CFP Corrected version of a pamphlet front page
CR1 Correction of entry in section i

Free format text: PAT. BUL. 24/2000 UNDER (30) REPLACE "NOT FURNISHED" BY "PCT/US99/28340"

WWE Wipo information: entry into national phase

Ref document number: 21681/00

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: PA/a/2001/005694

Country of ref document: MX

ENP Entry into the national phase

Ref country code: JP

Ref document number: 2000 586817

Kind code of ref document: A

Format of ref document f/p: F

WWE Wipo information: entry into national phase

Ref document number: 1999966036

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 1999966036

Country of ref document: EP

WWG Wipo information: grant in national office

Ref document number: 21681/00

Country of ref document: AU

WWW Wipo information: withdrawn in national office

Ref document number: 1999966036

Country of ref document: EP