EP1618143A2 - Thermoplastisches kunststoffmaterial aus nanoskaligen schichtverbindungen - Google Patents

Thermoplastisches kunststoffmaterial aus nanoskaligen schichtverbindungen

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Publication number
EP1618143A2
EP1618143A2 EP04742580A EP04742580A EP1618143A2 EP 1618143 A2 EP1618143 A2 EP 1618143A2 EP 04742580 A EP04742580 A EP 04742580A EP 04742580 A EP04742580 A EP 04742580A EP 1618143 A2 EP1618143 A2 EP 1618143A2
Authority
EP
European Patent Office
Prior art keywords
particles
composition according
lamellar compounds
nanometric lamellar
nanometric
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP04742580A
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English (en)
French (fr)
Inventor
Olivier Mathieu
Bruno Echalier
Bertrand Lousteau
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rhodia Engineering Plastics SpA
Original Assignee
Rhodia Engineering Plastics SpA
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
Application filed by Rhodia Engineering Plastics SpA filed Critical Rhodia Engineering Plastics SpA
Publication of EP1618143A2 publication Critical patent/EP1618143A2/de
Withdrawn legal-status Critical Current

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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
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/32—Phosphorus-containing compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18—Manufacture of films or sheets
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
    • 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

  • Thermoplastic material comprising nanoscale lamellar compounds
  • the present invention relates to materials comprising a thermoplastic matrix and at least particles based on zirconium phosphate, titanium, cerium and / or silicon in the form of nanometric lamellar compounds having a form factor of less than 100. These materials can in particular be used for the manufacture of plastic parts, such as for example films, sheets, tubes, hollow or solid body, bottles, pipes or tanks.
  • thermoplastic matrices such as in particular the barrier properties to gases or liquids or the mechanical properties.
  • lamellar nanofillers For the reduction of permeability, it is in particular possible to add lamellar nanofillers to the thermoplastic matrix. Such a decrease in permeability is attributed to a "tortuosity" effect caused by the lamellar nanofillers. Indeed, gases or liquids must travel a much longer path because of these obstacles arranged in successive strata.
  • Theoretical models consider that the barrier effects are all the more pronounced the higher the form factor, ie the length / thickness ratio.
  • the most explored lamellar nanofillers today are smectite-type clays, mainly montmorillonite.
  • the difficulty of implementation lies first of all in the more or less extensive separation of these individual sheets, that is to say the exfoliation, and their distribution, in the polymer.
  • intercalation which consists in swelling the crystals with organic cations, generally quaternary ammoniums, which compensate for the negative charge of the sheets.
  • These crystalline aluminosilicates when exfoliated in a matrix thermoplastic are in the form of individual lamellae whose form factor reaches values of the order of 500 or more.
  • fillers can be added, such as glass fibers or talc for example.
  • adding this type of filler in large proportions to obtain the required mechanical properties increases the density of the materials obtained.
  • thermoplastic matrix comprising particles based on zirconium phosphate, titanium, cerium and / or silicon, in the form of nanometric lamellar compounds, not exfoliated, exhibit good barrier properties to liquids and gases, and / or good mechanical properties, such as for example a good module / shock compromise, and / or a thermal resistance allowing its handling and its use at high temperatures.
  • the particles according to the present invention are present in the thermoplastic matrix in the form of nanometric lamellar compounds, that is to say in the form of a stack of several sheets.
  • thermoplastic matrix has the advantage of slightly modifying the rheology of said thermoplastic matrix.
  • thermoplastic compositions obtained thus have the fluidity and mechanical qualities required in the processing industry for these polymers.
  • composition with barrier properties to gases and liquids is intended to mean a composition which has reduced permeability vis-à-vis a fluid.
  • the fluid can be a gas or a liquid.
  • gases to which the composition has a low permeability there may be mentioned in particular oxygen, carbon dioxide and water vapor.
  • non-polar solvents in particular solvents representative of gasolines such as toluene, isooctane and / or polar solvents such as water and alcohols.
  • the present invention relates to a composition
  • a composition comprising at least one thermoplastic matrix and particles based on zirconium phosphate, titanium, cerium and / or silicon, in which at least 50% by number of the particles are in the form of nanometric lamellar compounds having a form factor less than or equal to 100.
  • nanometric lamellar compound means a stack of several lamellae, having a thickness of the order of several nanometers.
  • the nanometric lamellar compound according to the invention can be non-intercalated or else intercalated by an intercalating agent, also called a swelling agent.
  • form factor is meant the ratio of the largest dimension, generally the length, to the thickness of the nanometric lamellar compound.
  • the nanometric lamellar compound particles have a form factor less than or equal to 50, more preferably less than or equal to 10, particularly less than or equal to 5.
  • the nanometric lamellar compound particles have a form factor greater than or equal at 1.
  • a nanometric compound is understood to mean a compound having a dimension of less than 1 ⁇ m.
  • the particles of nanometric lamellar compounds of the invention have a length between 50 and 900 nm, preferably between 100 and 600 nm. ; a width between 100 and 500 nm; and a thickness between 50 and 200 nm (the length representing the longest dimension).
  • the different dimensions of the nanometric lamellar compound can be measured by transmission electron microscopy (TEM) or scanning electron microscopy (SEM).
  • the distance between the lamellae of the nanometric lamellar compound is between 5 and 15 ⁇ , preferably between 7 and 10 ⁇ . This distance between the lamellae can be measured by crystallographic analysis techniques, such as for example X-ray diffraction.
  • 50% by number of the particles are in the form of nanometric lamellar compounds having a form factor less than or equal to 100.
  • the other particles may in particular be in the form of individual lamellae, for example obtained by exfoliation of a nanometric lamellar compound.
  • At least 80% by number of the particles are in the form of nanometric lamellar compounds having a form factor less than or equal to 100, more preferably approximately 100% by number of the particles are in the form of nanometric lamellar compounds having a factor of form less than or equal to 100.
  • the particles according to the invention can optionally be assembled in the form of aggregates and / or agglomerates in the thermoplastic matrix. These aggregates and / or agglomerates can in particular have a dimension greater than one micron. It is also possible to use, for the present invention, particles based on zirconium phosphate, titanium, cerium and / or silicon of hydrated nanometric lamellar compounds, such as, for example, mono-hydrated or bi-hyd failed compounds.
  • zirconium phosphate is used according to the present invention, such as the ⁇ ZrP of formula Zr (HP0 4 ) 2 or ⁇ ZrP of formula
  • thermoplastic matrix it is also possible according to the invention to carry out a treatment with an organic compound of the particles based on zirconium phosphate, titanium, cerium and / or silicon before introduction into the thermoplastic matrix, in particular by an aminosilane compound, such as for example 3-aminopropylethoxysilane, or an alkylamine compound, such as for example pentylamine.
  • an aminosilane compound such as for example 3-aminopropylethoxysilane
  • alkylamine compound such as for example pentylamine
  • the composition according to the invention may comprise from 0.01 to 30% by weight of particles according to the invention relative to the total weight of the composition, preferably less than 10% by weight, more preferably from 0.1 to 10% by weight. weight, even more preferably from 0.1 to 5% by weight, particularly from 0.3 to 3% by weight, very particularly from 1 to 3% by weight.
  • the composition of the invention comprises as main constituent a thermoplastic matrix comprising at least one thermoplastic polymer.
  • the thermoplastic polymers are preferably chosen from the group comprising: polyamides, polyesters, polyolefins, poly (arylene) oxides, blends and copolymers based on these (co) polymers.
  • polymers of the invention there may be mentioned semi-crystalline or amorphous polyamides and copolyamides, such as aliphatic polyamides, semi-aromatic polyamides and more generally, linear polyamides obtained by polycondensation between a saturated aliphatic or aromatic diacid, and a diamine aromatic or aliphatic saturated primer, the polyamides obtained by condensation of a lactam, an amino acid or the linear polyamides obtained by condensation of a mixture of these different monomers.
  • semi-crystalline or amorphous polyamides and copolyamides such as aliphatic polyamides, semi-aromatic polyamides and more generally, linear polyamides obtained by polycondensation between a saturated aliphatic or aromatic diacid, and a diamine aromatic or aliphatic saturated primer, the polyamides obtained by condensation of a lactam, an amino acid or the linear polyamides obtained by condensation of a mixture of these different monomers.
  • these copolyamides can be, for example, the polyadipamide of hexamethylene, the polyphthalamides obtained from terephthalic and / or isophthalic acid, the copolyamides obtained from adipic acid, hexamethylene diamine and caprolactam.
  • the thermoplastic matrix is a polyamide chosen from the group comprising polyamide 6, polyamide 66, polyamide 11, polyamide 12, polymetaxylylenediamine (MXD6), blends and copolymers based of these polyamides.
  • polystyrene resin As other polymeric material, mention may also be made of polyolefins, such as polyethylene, polypropylene, polyisobutylene, polymethylpentene, their mixtures and / or copolymers.
  • Polypropylene is particularly preferred, which can be of the atactic, syndiotactic or isotactic type.
  • Polypropylene can in particular be obtained by polymerization of propylene with optionally ethylene, so as to obtain a polypropylene copolymer. Isotactic homopolymer polypropylene is preferably used.
  • composition according to the invention can optionally also comprise particles of nanometric lamellar compound comprising an intercalating agent which is inserted between the lamellae of the particles and / or an exfoliation agent which is capable of exfoliating the lamellae of the particles. , so as to completely separate the slats from one another, to obtain elementary slats.
  • These particles can be nanometric lamellar compounds based on zirconium phosphate, titanium, cerium and / or silicon, or any other type of compound such as: natural or synthetic clays of the smectite type such as for example montmorillonites, laponites, lucentiles, saponites, lamellar silicas, lamellar hydroxides, needle-like phosphates, hydrotalcites, apatites and zeolitic polymers.
  • natural or synthetic clays of the smectite type such as for example montmorillonites, laponites, lucentiles, saponites, lamellar silicas, lamellar hydroxides, needle-like phosphates, hydrotalcites, apatites and zeolitic polymers.
  • the intercalation and / or exfoliation agents can be chosen from the group consisting of: NaOH, KOH, LiOH, NH 3) monoamines such as n-butylamine, diamines such as hexamethylene diamine, methyl-2- pentamethyiene diamine, amino acids such as amino caproic acid and amino undecanoic acid, and amino alcohols such as triethanolamine.
  • composition of the invention may also comprise other additives generally used in compositions based on a thermoplastic matrix, such as for example: stabilizers, nucleators, plasticizers, flame retardants, stabilizers for example of the HALS type, antioxidants, anti-UV, dyes, optical brighteners, lubricants, anti-bonding agents, matting agents such as titanium oxide, processing agents, elastomers or compositions of elastomers, for example ethylene propylene copolymers optionally functionalized by grafting (maleic anhydrous, glycidyl), olefin and acrylic copolymers or copolymers of butadiene methacrylate and styrene, adhesion agents, for example polyolefins grafted with maleic anhydride allowing adhesion to polyamide, dispersing agents, active oxygen sensors or absorbers, and / o u catalysts.
  • additives generally used in compositions based on a thermoplastic matrix
  • additives such as for example: stabilize
  • composition of the invention can also comprise reinforcing additives, minerals such as alumino-silicate clays (intercalated or not, exfoliated or no), kaolin, talcs, calcium carbonates, fluoro-micas, calcium phosphates and derivatives, fibrous reinforcements such as glass fibers, aramid fibers and carbon fibers.
  • minerals such as alumino-silicate clays (intercalated or not, exfoliated or no), kaolin, talcs, calcium carbonates, fluoro-micas, calcium phosphates and derivatives, fibrous reinforcements such as glass fibers, aramid fibers and carbon fibers.
  • thermoplastic composition Any method known to those skilled in the art for obtaining a dispersion of compounds in a thermoplastic composition can be used to make the composition according to the present invention.
  • a first method consists in mixing at least particles based on zirconium phosphate, titanium, cerium and / or silicon in the form of nanometric lamellar compounds, with monomers and / or oligomers of a thermoplastic matrix, before or during the polymerization step, and then proceed to polymerization.
  • the polymerization processes used in the context of this embodiment are the usual processes.
  • the polymerization can be interrupted at an average degree of progress and / or can be continued in the solid state by known post-condensation techniques.
  • Another method consists in mixing at least particles based on zirconium phosphate, titanium, cerium and / or silicon in the form of nanometric lamellar compounds with a thermoplastic matrix, in particular in molten form, and optionally subjecting the mixture to shearing , for example in an extrusion device, in order to achieve good dispersion.
  • a twin-screw extruder of the ZSK30 type into which a polymer in the molten state and the nanometric lamellar compound according to the invention are introduced, for example, in the form of powder. It is possible that said powder comprises aggregates and / or agglomerates of particles according to the invention.
  • Another method consists in mixing a thermoplastic matrix, in particular in molten form, and at least one composition, such as for example a concentrated mixture, comprising at least particles based on zirconium phosphate, titanium, cerium and / or silicon under the form of nanoscale lamellar compounds, and a thermoplastic matrix, said composition being able to be prepared for example according to one of the methods described above.
  • a thermoplastic matrix in particular in molten form
  • at least one composition such as for example a concentrated mixture, comprising at least particles based on zirconium phosphate, titanium, cerium and / or silicon under the form of nanoscale lamellar compounds, and a thermoplastic matrix, said composition being able to be prepared for example according to one of the methods described above.
  • the nanometric lamellar compound can be introduced into the synthesis medium of the thermoplastic polymer, or into a molten thermoplastic polymer.
  • barrier materials based on polyamide an advantageous embodiment consists in introducing into the polymerization medium a disper
  • the nanometric lamellar compounds used in the process according to the invention can be non-intercalated and / or intercalated. In all cases, the addition of an intercalation and / or exfoliation agent in the nanometric lamellar compound must not lead to a total exfoliation of said nanometric lamellar compound so as to obtain the composition according to the invention such that previously defined.
  • the invention also relates to articles obtained by shaping the composition of the invention, by any thermoplastic transformation technique, such as for example by extrusion, such as for example extrusion of sheets and films or extrusion blow molding; by molding such as for example compression molding, thermoforming or rotational molding; by injection such as for example by injection molding or by blow molding.
  • the preferred articles of the invention are in particular parts, films, sheets, tubes, hollow or solid body, bottles, pipes and / or tanks. These articles can be used in many fields such as for example the automobile, such as fuel lines or tanks, injection rails, parts coming into contact with gasolines such as pump elements, containers, packaging, such as for example the packaging of solid or liquid foodstuffs, the packaging of cosmetics, bottles and films.
  • These articles can also be used for the packaging of raw materials, for example thermosetting composites based on polyester filled with glass fibers, for molding, bitumen sheets, or even as a protective or separation film during processing operation, for example for vacuum molding.
  • composition according to the present invention can be deposited, or associated with another substrate, such as thermoplastic materials for the manufacture of composite articles.
  • This deposit or association can be made by known methods of co-extrusion, lamination, coating, overmolding, co-injection and multi-layer blow molding injection.
  • Multilayer structures can be formed from one or more layers of material according to the invention. These layers can be combined by layers of coextrusion binder with one or more other layers of one or more thermoplastic polymers, for example polyethylene, polypropylene, polyvinyl chloride, polyethylene terephthalate.
  • the films or sheets thus obtained can be mono-stretched or bi-stretched according to known techniques for transforming thermoplastics.
  • the sheets or plates can be cut, thermoformed and / or stamped to give them the desired shape.
  • Example 1 Preparation of a compound based on crystallized zirconium phosphate. The following reagents are used:
  • the cake is dispersed in 1 liter of 10 M aqueous phosphoric acid solution, the dispersion thus obtained is transferred to a 2 liter reactor and then heated to 115 ° C. This temperature is maintained for 5 hours.
  • the dispersion obtained is washed by centrifugation with deionized water to a conductivity of less than 1 mS for the supernatant.
  • a cake based on crystallized zirconium phosphate is obtained.
  • the cake from the last centrifugation is redispersed in water so as to obtain a solution giving a dry extract close to 20%, the pH of the dispersion is between 1 and 2.
  • a dispersion of a crystallized compound based on zirconium phosphate is obtained, the characteristics of which are as follows:
  • TEM Transmission Electronic Microscope
  • Example 2 Process for the manufacture of ⁇ ZrP interspersed with an organic base (Step c)
  • Example 1 The product from Example 1 is neutralized by adding hexamethylene diamine (HMD): to the dispersion is added an aqueous solution of HMD at 70% up to obtaining a pH of 5. The dispersion thus obtained is homogenized using an Ultraturax. The final dry extract is adjusted by adding deionized water (dry extract: 15% by weight). The product obtained is called ZrPi (HMD).
  • HMD hexamethylene diamine
  • a polyamide 6 having a viscosity index of 200 ml / g measured in formic acid is synthesized from caprolactam according to a conventional process. This polyamide 6 is called material A. The granules obtained are called granules A.
  • a polyamide 6 is also synthesized having a viscosity index of 200 ml / g measured in formic acid (Standard ISO EN 307) from caprolactam according to a conventional method, by introducing into the polymerization medium an aqueous dispersion comprising either ZrPi HMD from Example 2 or ZrP from Example 1. 1% or 2% by weight of ZrP or ZrPi HMD are thus introduced, by relative to the total weight of the polyamide.
  • Granules B include ZrP from Example 1.
  • Granules C include ZrPi HMD from Example 2. The granules are washed to remove residual caprolactam. For this purpose, the granules are immersed in boiling water for two times 8 hours, then are dried under primary vacuum ( ⁇ 0.5 mbar) for 16 hours at 110 ° C.
  • a transmission microscopy analysis of the granules B shows that the ZrP introduced during the polymerization of the polyamide remains in the form of a nanometric lamellar compound (sheets) in the polyamide matrix. There was therefore no exfoliation of the ZrP during the polymerization.
  • the form factor calculated from the measurements of the thickness and the length of the nanometric lamellar compounds is 3.
  • Test pieces are produced from granules A, B or C. The test pieces have a width of 10 mm, a length of 80 mm and a thickness of 4 mm. The test pieces are conditioned at 28 ° C and 0% relative humidity. Various tests were carried out on the test pieces according to the measurement methods indicated below to determine the mechanical properties of the materials:
  • HDT-Heat Deflection Temperature measured according to ISO 75, under load of 1.81 N / mm 2 .
  • the Melt Flow Index is measured according to ISO 133 after drying the polymer overnight at 110 ° C at 0.267 mbar, the viscometer used is a Gôttfert MPSE with a 2 mm die.
  • the MFI is expressed in g / 10 min. The measurements are carried out at 275 C with a load of 2160 g.
  • the granules A, B or C from Example 3 are shaped by extrusion on an apparatus of the Mac.Gi brand type TR 35/24 GM, the tubes produced having a thickness of 1 mm (external diameter of 8 mm; internal diameter of 6 mm).
  • the diameter and thickness of the tubes being measured before carrying out the permeability tests.
  • the tubes produced include 3 identical layers (inner, outer and central layer).
  • the tubes are then stored for 48 hours at 23 ° C and 0% RH (relative humidity).
  • the breaking stress is measured on an Instron 4500 (force cell 100
  • Example 5 Permeability to M15 gasoline and unleaded gasoline
  • the permeability of the various materials to M15 gasoline was evaluated by measuring the weight loss as a function of time.
  • the various tubes of Example 4 are dried in a vacuum oven at 70 ° C for 12 hours.
  • the different tubes are filled with M15 petrol or unleaded petrol and the tubes are sealed.
  • the tubes thus filled are weighed on a precision balance.
  • the tubes are then placed in an oven at 40 ° C. for 45 days. At regular time intervals the tubes are weighed and the loss in mass noted. Permeability is therefore measured statically.
  • M15 gasoline consists of: 15% methanol, 42.5% toluene, and 42.5% isooctane (trimethyl-2,2,4 pentane).
  • the weight loss versus time curve is broken down into two phases: a first induction phase (corresponding to the diffusion of the fluid through the wall of the tube), then a second phase of reduction in the weight of the tubes
  • the permeability measured in g.mm/m 2 / day, is calculated from the slope of the
  • Example 6 Barrier film comprising zirconium phosphate.
  • the polymer granules from Example 3 are shaped by extrusion on an apparatus of the CMP brand.
  • the oxygen transmission coefficient is measured according to standard ASTM D3985 under the following specific conditions. Measurement conditions:
  • the preparation ⁇ ZrP is carried out as mentioned in Example 1 except that during the crystallization step of step b) the cake is dispersed in 1 liter of an aqueous solution of 12.6 M phosphoric acid. , the dispersion thus obtained being transferred to a 2 liter reactor and then heated to 125 ° C. The other steps of the process are preserved.
  • Example 2 One thus obtains an ⁇ ZrP similar to Example 1 with, however, obtaining a lamellar structure whose lamellae have a size of between 300 and 500 nm.
  • the dispersion is then dried in an oven for 15 h at 90 ° C.
  • the dry product as well is a powder called ZrP.
  • Example 8 Process for the Manufacture of ⁇ ZrP Powder Treated with an Aminosilane
  • the dispersion thus obtained is washed to remove the residual alcohol and then dried in an oven for 15 h at 90 ° C.
  • the product thus obtained is called ZrP / aminosilane.
  • a nanocomposite based on polypropylene (PP) and ZrP from Examples 7 or 8 is produced under the following conditions.
  • a mixture is made comprising 96.8% of polypropylene resin isotactic homopolymer in granules of melt flow index (according to ISO 1133) of 3 g / 10 min at 230 ° C under 2.16 kg of load, 3% of load mineral dried in an oven 16 h at 90 ° C and 0.2% of antioxidant Irganox B225, in a Brabender mixer equipped with W50 rotors with a rotational speed of the rotors of 125RPM, a filling coefficient of 0.7, a tank temperature of 150 ° C, for a time of 5 min.
  • test pieces are thermoformed in a press for 10 minutes at 200 ° C under a pressure of 200 bars and then cooled for 4 minutes to 200 bars at 15 ° C to form plates of 100 mm by 100 mm by 4 mm.
  • Test pieces of dimension 80 mm by 10 mm by 4 mm are then cut. Analysis by transmission microscopy of the test pieces shows that the ZrP and the ZrP / aminosilane introduced into the polypropylene remains in the form of a nanometric lamellar compound (sheets) with a form factor of less than 100.
  • These test pieces are characterized in three-point bending, according to ISO 178 standard and Charpy impact notched according to ISO 179.
  • the test conditions used are as follows: - Three-point bending: 5 test pieces of ISO dimensions tested at 23 ° C under the conditions established by ISO 178.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
EP04742580A 2003-04-28 2004-04-27 Thermoplastisches kunststoffmaterial aus nanoskaligen schichtverbindungen Withdrawn EP1618143A2 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0305165 2003-04-28
PCT/FR2004/001013 WO2004096903A2 (fr) 2003-04-28 2004-04-27 Materiau thermoplastique comprenant des composes lamellaires nanometriques

Publications (1)

Publication Number Publication Date
EP1618143A2 true EP1618143A2 (de) 2006-01-25

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Country Status (10)

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US (1) US20070082159A1 (de)
EP (1) EP1618143A2 (de)
JP (1) JP4425908B2 (de)
KR (1) KR100779446B1 (de)
CN (1) CN1798801A (de)
BR (1) BRPI0410518A (de)
MX (1) MXPA05011562A (de)
RU (1) RU2326138C2 (de)
UA (1) UA83366C2 (de)
WO (1) WO2004096903A2 (de)

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MXPA05011562A (es) 2007-01-31
UA83366C2 (uk) 2008-07-10
US20070082159A1 (en) 2007-04-12
BRPI0410518A (pt) 2006-06-20
CN1798801A (zh) 2006-07-05
KR20060041162A (ko) 2006-05-11
RU2326138C2 (ru) 2008-06-10
RU2005136878A (ru) 2007-10-27
KR100779446B1 (ko) 2007-11-28
JP2006524732A (ja) 2006-11-02
JP4425908B2 (ja) 2010-03-03
WO2004096903A2 (fr) 2004-11-11
WO2004096903A3 (fr) 2005-07-14

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