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EP1349807A1 - Composes mineraux, leur procede de preparation et leur utilisation dans les materiaux thermoplastiques - Google Patents

Composes mineraux, leur procede de preparation et leur utilisation dans les materiaux thermoplastiques

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Publication number
EP1349807A1
EP1349807A1 EP01965341A EP01965341A EP1349807A1 EP 1349807 A1 EP1349807 A1 EP 1349807A1 EP 01965341 A EP01965341 A EP 01965341A EP 01965341 A EP01965341 A EP 01965341A EP 1349807 A1 EP1349807 A1 EP 1349807A1
Authority
EP
European Patent Office
Prior art keywords
compound
titanium
zirconium phosphate
zirconium
functions
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Withdrawn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
EP01965341A
Other languages
German (de)
English (en)
French (fr)
Inventor
Emmanuelle Bougelot
Dominique Dupuis
Gilles Robert
Jo[L Varlet
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.)
Rhodianyl SAS
Original Assignee
Rhodianyl SAS
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 Rhodianyl SAS filed Critical Rhodianyl SAS
Publication of EP1349807A1 publication Critical patent/EP1349807A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B25/00Phosphorus; Compounds thereof
    • C01B25/16Oxyacids of phosphorus; Salts thereof
    • C01B25/26Phosphates
    • C01B25/37Phosphates of heavy metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/32Phosphorus-containing compounds
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B25/00Phosphorus; Compounds thereof
    • C01B25/16Oxyacids of phosphorus; Salts thereof
    • C01B25/26Phosphates
    • C01B25/37Phosphates of heavy metals
    • C01B25/372Phosphates of heavy metals of titanium, vanadium, zirconium, niobium, hafnium or tantalum
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/10Metal compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers

Definitions

  • the present invention relates to a mineral compound with a lamellar structure, its preparation process, and its use for the reinforcement of macromolecular materials. It relates more precisely to a compound based on zirconium phosphate and / or titanium.
  • thermomechanical properties of macromolecular materials it is known to use mineral particles. It is thus possible to modify, for example, the modulus of the materials, the impact resistance, the ductility, the dimensional stability, the deformation temperature under load, the resistance to abrasion or the abrasive power. It is known to reinforce macromolecular materials, and in particular thermoplastic materials, with platelet particles of nanometric thickness. Such particles can for example be obtained by exfoliation from an inorganic compound with a lamellar structure. This is the case for example for the particles obtained from montmorillonite.
  • montmorillonite which has a lamellar structure
  • an organic swelling agent which is inserted between the lamellae and separates them from one another, in order to promote their exfoliation.
  • the organic agent often comprises an ammonium group, and at least one relatively long chain.
  • the preferred ammoniums are quaternary ammoniums.
  • Japan JP05306370 describes the use of platelet particles obtained by exfoliation from a compound based on zirconium phosphate with a lamellar structure.
  • the compound with a lamellar structure is treated with an organic swelling agent, before incorporation into polyamide, in order to ensure its exfoliation.
  • exfoliation of these mineral compounds with a lamellar structure is important for improving the thermomechanical properties of the macromolecular materials in which they are introduced. This exfoliation is favored in particular by the prior treatment of the mineral compounds with often bulky organic swelling agents, as indicated in the state of the art described above.
  • the preliminary treatment of the mineral compound with these organic blowing agents can sometimes have drawbacks. On the one hand, this involves an additional step in the process of manufacturing the final material, between the synthesis or the extraction of the compound with a lamellar structure, and its use for example as reinforcement.
  • the presence of the organic swelling agent can induce difficulties during the incorporation of the compound, or during the processes for shaping the materials.
  • the organic swelling agent can be degraded during these operations and thus either deteriorate the quality of the macromolecular compound in which it is used, or lose its potential for assisting exfoliation.
  • the compounds used are generally smelly, which makes their handling unpleasant, or requires high investment to overcome the odor. This is a particular case for agents comprising an ammonium group.
  • the object of the present invention is to provide new lamellar compounds based on zirconium phosphate and / or titanium having good exfoliation properties, and a process for preparing this compound comprising a treatment which does not have the drawbacks mentioned above. above. It also aims to propose new macromolecular materials comprising these lamellar compounds.
  • the invention firstly provides a compound based on zirconium phosphate and / or titanium comprising a compound according to the following formula (I): A-R-B (I) in which
  • a and B are functions, identical or different, capable of reacting with the acid functions of zirconium phosphate and / or titanium
  • R is an aliphatic, cycloaliphatic or aromatic hydrocarbon radical, substituted or not, comprising from 2 to 20 atoms of carbon, and which may include heteroatoms characterized in that the molar ratio ⁇ between the number of moles of functions A and B and the number of moles of zirconium phosphate and / or titanium being between 0.1 and 0.8.
  • a process for preparing the above compound optionally dispersed in a liquid comprising the following successive steps: a) Precipitation in an acid medium of a compound based on zirconium phosphate and / or titanium, starting from phosphoric acid and a zirconium compound and / or a titanium-based compound or mixed titanium-zirconium-based compounds, the titanium and / or zirconium being at oxidation state IV b) Crystallization of the compound c) Treatment of the crystallized compound, in a liquid medium, at a pH between 3 and 9.
  • compositions comprising a macromolecular material, preferably a thermoplastic polymer and, the lamellar compound, dispersed at least partially under form of sheets in the composition.
  • a process for manufacturing compositions comprising a thermoplastic matrix and a lamellar compound, as well as the compositions obtained according to this process, the lamellar compound being dispersed at least partially in the form of sheets in the composition.
  • the compound of formula (I), present in the compound based on zirconium phosphate and / or titanium of the first subject of the invention, comprises two functions A and B capable of reacting with the acid functions of zirconium phosphate and / or titanium.
  • the functions A and B can for example be basic functions capable of reacting with the protons of zirconium phosphate and / or of titanium. Functions A and B and
  • B are preferably in neutral or positively charged form.
  • functions A and B which may be suitable for the invention, mention may be made of amines, ammoniums, phosphoniums.
  • the functions A and B are amino functions.
  • the compound (I) is chosen from hexamethylene diamine, methyl-2-pentamethylene diamine, metaxylene diamine.
  • the molar ratio ⁇ between the number of moles of functions A and B and the number of moles of zirconium and / or titanium phosphate is between 0.1 and 0.8.
  • number of moles of functions A and B is meant the sum of the number of moles of functions A and the number of moles of functions B.
  • one mole of compound of formula (I) corresponds to two moles of functions A and B .
  • number of moles of zirconium and / or titanium phosphate is meant the number of moles of phosphorus element.
  • one mole of zirconium phosphate compound generally corresponds to two moles of phosphorus element.
  • the molar ratio ⁇ is between 0.4 and 0.6.
  • the molar ratio ⁇ is substantially equal to 0.5.
  • the compound based on zirconium phosphate and / or titanium has a interleaf distance less than or equal to 15 ⁇ .
  • the radical R is not reactive with respect to the acid functions of zirconium phosphate and / or titanium, nor with respect to phosphate in general.
  • the second object of the invention relates to a process for the preparation of the above compound.
  • the preparation process according to the invention comprises at least the three successive stages a), b), and c). It may include other steps or phases of the process before, after or between these steps. These are, for example, washing, purification, filtration, dilution, centrifugation, addition of compounds in order to regulate certain process parameters such as pH, ionic strength.
  • steps or phases of the process before, after or between these steps are, for example, washing, purification, filtration, dilution, centrifugation, addition of compounds in order to regulate certain process parameters such as pH, ionic strength.
  • the implementation of such process phases will appear in particular in the light of the examples which are presented below.
  • Step a) consists of a precipitation of a compound based on zirconium phosphate and / or titanium.
  • the preparation of such precipitates is known to those skilled in the art. It is carried out from phosphoric acid and a zirconium compound and / or a titanium compound, the zirconium and / or titanium being at the oxidation state IV. Mention is made of zirconium and / or titanium tetra-halides, zirconium and / or titanium oxyhalides, in particular zirconium oxychloride and titanium oxychloride. Mixed compounds based on zirconium and titanium can also be used.
  • a simplified assessment of the precipitation reaction is, for example, as follows: 2 H 3 P0 4 + ZrOCI 2 ⁇ Zr (H + , PO 4 3 " ) 2 + 2 HCI
  • the precipitation is preferably carried out in an aqueous medium.
  • the use of phosphoric acid induces an acidity of the precipitation medium.
  • the precipitation can advantageously be carried out at acid pH, preferably controlled, for example between
  • An acid can be used for this purpose, in addition to the precursors of the precipitate. Mention is made, for example, of hydrochloric acid.
  • the precipitate can crystallize in a lamellar structure, at room temperature, without it being necessary to carry out a crystallization operation distinct from the precipitation step.
  • the crystallization can be carried out by hot treatment in water or in an aqueous solution, for example by immersion of the compound in water at a temperature between 100 ° C and 200 ° C.
  • the crystallization is preferably carried out in an acidic aqueous solution, for example a phosphoric acid solution.
  • the crystallization time can be several hours.
  • the crystallization step is advantageously preceded by a phase for washing the precipitate, making it possible inter alia to eliminate the ionic species resulting from the precipitation reaction.
  • the crystallization step is advantageously followed by a washing and centrifugation phase.
  • the pH measured in the aqueous phase of a dispersion comprising the crystallized compound, at 20% by weight in dry extract is between 0.5 and 2.
  • the lamellar compound is never dried, the only operations for removing water being filtration or centrifugation operations.
  • drying operation is understood here to mean an operation during which the compound is introduced into a hot atmosphere and devoid of water, for a period greater than 15 minutes, for example in an oven.
  • the compound crystallizes in the ⁇ phase of zirconium phosphate.
  • the structure of this phase has for example been described in J. Inorg. Nucl. Chem vol 26, p 117-129.
  • This phase has a lamellar structure, with protons interposed between the lamellae. Without wishing to be bound by any theory, it is believed that these protons can be exchanged by a positively charged chemical species.
  • Treatment step c) consists in treating the compound, crystallized, in a liquid medium, at a pH of between 3 and 9.
  • the liquid medium is preferably an aqueous solution, in which the zirconium phosphate-based compound is dispersed.
  • the aqueous solution comprises a mineral or organic compound of a nature and / or in an amount such that the pH is between 3 and 9. According to a preferred characteristic, the pH is between 4 and 7.
  • the mineral or organic compound is chosen from the compounds which, in aqueous solution, have a pH greater than 3, preferably greater than 7.
  • the compound is generally the compound of formula (I) described above, corresponding to the compound based on zirconium phosphate and / or titanium which it is desired to prepare.
  • the use of these organic compounds can be very particularly indicated for the use of the compound with a lamellar structure for the reinforcement of polyamides.
  • the organic compound is hexamethylene diamine.
  • the mineral compound for the treatment at a pH of between 2 and 7 can also be chosen from hydroxides of metals, alkalis, or alkaline earths, for example sodium hydroxide; the mineral compounds of the ammonium ion, such as ammonium hydroxide; lithium, sodium, potassium cations in the presence, optionally, of a basic agent.
  • the organic compound can be for example caprolactam or ammonia. These compounds may be indicated for the use of the compound with a lamellar structure for the reinforcement of polyamides.
  • the compound can be washed and / or separated from the liquid medium, for example by filtration, evaporation of the liquid medium, preferably evaporation of water. It can also be dried.
  • a mineral compound with a lamellar structure is thus obtained which can easily exfoliate into platelet particles.
  • the compound can be packaged in different forms. It can be packaged in powder form, after elimination of the liquid medium, and optionally drying. It can be packaged in the form of a dispersion in a liquid medium, for example water.
  • the form of packaging generally depends on the use for which it is intended.
  • the compound can be advantageously introduced in the form of a dispersion in the medium for synthesis of the polymer.
  • the compound is introduced in the form of a dispersion into the medium containing the monomers at the origin of the synthetic polymer.
  • the third subject of the invention relates to compositions comprising a matrix consisting of a macromolecular material, and a lamellar compound based on zirconium phosphate and / or titanium, dispersed at least partly in the form of sheets in the matrix.
  • the lamellar compound is the compound described above.
  • the macromolecular material can be of different natures: elastomeric, thermoplastic, thermoset.
  • the macromolecular material is preferably a thermoplastic polymer.
  • polymers which may be suitable, mention is made of: polylactones such as poly (pivalolactone), poly (caprolactone) and polymers of the same family; polyurethanes obtained by reaction between diisocyanates such as 1,5-naphthalene diisocyanate; p-phenylene diisocyanate, m-phenylene diisocyanate, 2,4-toluene diisocyanate, 4,4'-diphenylmethane diisocyanate, 3,3'-dimethyl-4,4'-diphenylmethane diisocyanate, 3, 3-'dimethyl-4,4'-biphenyl diisocyanate, 4,4'- diphenylisopropylidene diisocyanate, 3,3'-dimethyl-4,4'-dipheny
  • polyamides are particularly preferred, such as polyamide 6, polyamide 66, semi-aromatic polyamides, PVC, PET, PPO and mixtures and copolymers based on these polymers.
  • compositions can also comprise other additives, such as for example stabilizers, plasticizers, flame retardants, dyes, lubricants, catalysts. This list is in no way limiting. They may also include other reinforcing additives such as impact resistance modifiers such as optionally grafted elastomers, mineral reinforcements such as clays, kaolin, fibrous reinforcements such as glass fibers, aramids, carbon fibers.
  • additives such as for example stabilizers, plasticizers, flame retardants, dyes, lubricants, catalysts. This list is in no way limiting. They may also include other reinforcing additives such as impact resistance modifiers such as optionally grafted elastomers, mineral reinforcements such as clays, kaolin, fibrous reinforcements such as glass fibers, aramids, carbon fibers.
  • a first method consists in mixing the lamellar compound in a thermoplastic material in molten form and optionally subjecting the mixture to significant shearing, for example in a twin-screw extrusion device, in order to achieve good dispersion.
  • Another method consists in mixing the compound to be dispersed with the monomers in the polymerization medium, then in carrying out the polymerization.
  • Another method consists in mixing with a thermoplastic polymer in molten form, a concentrated mixture of a thermoplastic polymer and dispersed particles, prepared for example according to one of the methods described above.
  • the lamellar compound is introduced into the synthesis medium of the macromolecular compound, or in a molten thermoplastic polymer. It can for example be introduced in the form of a solid powder or in the form of a dispersion in water or in an organic dispersant.
  • an advantageous embodiment consists in introducing into the polymerization medium a dispersion in water of the lamellar compound based on zirconium phosphate.
  • the dispersion can be introduced into the medium comprising the monomers of the polyamide to be manufactured.
  • the polymerization processes used in the context of this embodiment are the usual processes.
  • the proportion by weight of the lamellar compound in the composition is preferably less than or equal to 5%.
  • the fourth subject of the invention relates to a process for manufacturing a composition comprising a thermoplastic matrix and a compound based on zirconium phosphate and / or titanium according to which a compound based on zirconium phosphate and / or titanium having a interleaf distance of less than or equal to 15 ⁇ in the matrix or in the polymerization medium of the matrix.
  • This compound based on zirconium phosphate and / or titanium comprises an inorganic or organic compound comprising at least one function capable of reacting with the acid functions of zirconium phosphate and / or titanium.
  • an inorganic or organic compound can be in the form of a cation.
  • mineral compound in cationic form there may be mentioned, by way of example, metal cations, alkaline cations such as Na + , K + , Li + , the ammonium ion NH 4 + . Without wishing to be bound by any theory, it is believed that such cations can be exchanged with the protons of zirconium and / or titanium phosphate.
  • a cation such as Na + , K + , Li + or NH 4 + corresponds to a function capable of reacting with the acid functions of zirconium and / or titanium phosphate.
  • the mineral compound is the Na + ion.
  • the mineral or organic compound comprises a function capable of reacting with the acid functions of zirconium and / or titanium phosphate.
  • This function can be a basic function.
  • basic function one can cite for example the amino function.
  • the function can for example be in a neutral form or positively charged.
  • the organic compound is a monoamine. It may for example be an aliphatic monoamine such as n-butylamine.
  • the organic compound is an amino acid or a lactam. Mention may be made, for example, of caprolactam.
  • the mineral or organic compound comprises two functions capable of reacting with the acid functions of zirconium and / or titanium phosphate.
  • organic compound is a compound according to the following formula (II): ARB (II) in which
  • a and B are functions, identical or different, capable of reacting with the acid functions of zirconium phosphate and / or titanium,
  • R is an aliphatic, cycloaliphatic or aromatic hydrocarbon radical, substituted or not, comprising from 2 to 20 atoms of carbon, and may include heteroatoms
  • the molar ratio ⁇ between the number of moles of functional groups capable of reacting with the mineral or organic compound and the number of moles of zirconium and / or titanium phosphate is between 0, 1 and 0.8.
  • number of moles of functions capable of reacting means the sum of the number of moles of each function of the mineral or organic compound capable of reacting.
  • the number of moles of functions capable of reacting corresponds to the number of moles of the compound.
  • the number of moles of functions capable of reacting corresponds to twice the number of moles of the compound.
  • number of moles of zirconium and / or titanium phosphate is meant the number of moles of phosphorus element.
  • one mole of zirconium phosphate compound generally corresponds to two moles of phosphorus element.
  • the ⁇ molar ratio is between 0.4 and 0.6.
  • the molar ratio ⁇ is substantially equal to 0.5.
  • the compound based on zirconium phosphate and / or titanium having an interleaf distance less than or equal to 15 ⁇ is obtained by the process for preparing the second object of the invention.
  • the inorganic or organic compound of treatment step c) is suitably chosen as a function of the compound based on zirconium phosphate and / or titanium which it is desired to prepare.
  • the invention also relates to the compositions obtained by the process for manufacturing the fourth object of the invention, at least part of the compound based on zirconium phosphate and / or titanium being dispersed in the form of sheets in the composition. All that has been described above concerning the compositions of the third object of the invention is valid here identically for the compositions obtained by the method of the fourth object of the invention, in particular what relates to the nature of the matrix, to the proportion of the compound based on zirconium phosphate and / or titanium in the composition, and to the addition of other additives.
  • the invention also relates in a fifth object to the articles shaped from the compositions of the invention described above in the third and the fourth object of the invention.
  • the articles can be shaped by molding or spinning.
  • the methods of manufacturing molded articles that can be used are, for example, injection, extrusion, extrusion blow-molding methods.
  • the invention also relates to yarns, fibers or filaments consisting of a composition of the invention.
  • the spun articles, threads, fibers or filaments are produced according to the usual spinning techniques from a material comprising a thermoplastic polymer and the compound based on zirconium phosphate and / or titanium. Spinning can be carried out immediately after the polymerization of the thermoplastic polymer, the latter being in molten form. It can be produced from a granulated composite comprising the compound and the polymer. The compound can be incorporated into the molten polymer before the spinning operation, as a concentrated mixture in a polymer. All modes of incorporating the compound into a spinning polymer can be used.
  • the yarns, fibers or filaments according to the invention can be subjected to all the treatments that can be carried out in steps subsequent to the spinning step. They can in particular be stretched, textured, crimped, heated, twisted, dyed, sized, cut, etc. These additional operations can be carried out continuously and can be integrated after the spinning device or be carried out discontinuously.
  • the list of post-spinning operations has no limiting effect.
  • the yarns, fibers or filaments according to the invention can be used in woven, knitted or non-woven form.
  • the fibers according to the invention are in particular suitable for the manufacture of felts for paper machines. They can also be used for the manufacture of carpet yarns.
  • platelet particles based on zirconium phosphates makes it possible to improve the abrasion resistance of a material. This improvement is particularly advantageous in the context of the use of the material in the form of threads, fibers or filaments.
  • the precipitate is washed by centrifugation at 4500 rpm, with 1200 ml of H 3 PO 20 g / L then with deionized water, until a conductivity of 6.5 mS (supernatant) is reached. A cake of the precipitate based on zirconium phosphate is obtained.
  • 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 (supernatant).
  • the cake from the last centrifugation is redispersed so as to obtain 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, of which the characteristics are as follows:
  • Examples 2-3 Treatment of the compound with a mineral base (Step c) 805 g (in dry extract) of product from Example 1 are centrifuged. The centrifugation pellet is redispersed in an aqueous sodium hydroxide solution at 10 "3 mol / L (500 ml). Three washes are carried out under these same conditions. The cake resulting from the last centrifugation is redispersed in 500 ml of sodium hydroxide solution. 10 "3 mol / L. The pH is adjusted to 5 (example 2) or to 3 (example 3) by adding 8 mol / l sodium hydroxide. The dispersion is centrifuged and the pellet is redispersed in 300 ml of purified water (dry extract: 30% by weight). The final conductivity of the suspension is less than 1 mS.
  • Example 2 The product from Example 1 is neutralized by adding hexamethylene diamine: To the dispersion is added an aqueous solution of HMD at 70% until a pH of 5 is obtained. The dispersion thus obtained is homogenized with using an Ultraturax. The final dry extract is adjusted by adding deionized water (dry extract: 15% by weight).
  • Example 5 Treatment of the compound with caprolactam (Step c)) Caprolactam is incorporated into the mineral sol obtained according to example 1 (33% by weight of caprolactam relative to the dry extract). The pH measured in the solution is 3.3. Then by distillation of the water, a powder is recovered containing the corresponding fraction of caprolactam.
  • Examples 6-10 Compositions comprising platelet particles based on zirconium phosphate.
  • a polyamide 6 is synthesized from caprolactam according to a conventional process, by introducing into the polymerization medium an aqueous dispersion obtained in examples 2 to 4, or the powder obtained in example 5. The proportion of compound based of zirconium phosphate introduced is 2% by weight.
  • a polymer is also synthesized that does not contain the compound (Example 10, comparative). After polymerization, the polymer is formed into granules. These are washed to remove the residual caprolactam (the granules are immersed in an excess of water at 90 ° C for a few hours) and are then dried under primary vacuum ( ⁇ 0.5 mbar) for 16 hours at 110 ° C.
  • Tensile tests are carried out on extruded rods and conditioned for 30 days at 50% RH and 23 ° C.
  • the diameter of the rods is between 0.5 and 1 mm.
  • An INSTRON 1185 traction machine is used with a force sensor with a capacity of 100 N.
  • the nominal stress is reported (ratio of the force measured over the section evaluated by diameter measurement with Palmer) as a function of the relative deformation applied. The results are reported in Table 1.
  • a composition based on polyamide is obtained whose elongation at break is greater than that of a polyamide not comprising the mineral compound, and whose modulus is improved.
  • FIG. 1 represents a photograph of a composition observed under the microscope comprising the zirconium phosphate compound corresponding to example 2.
  • FIG. 2 represents a photograph of a composition observed under the microscope comprising the zirconium phosphate compound corresponding to example 4.
  • Example 11-14 Filaments Monofilaments with a diameter of approximately 250 ⁇ m are spun at low speed from a composition according to Example 9, or from a pure polyamide according to Example 10. The monofilaments are stretched. in recovery at different drawing rates. The mechanical properties and the abrasion resistance of the monofilaments are evaluated according to the following tests:
  • the initial length of the wires is 50 mm and the crosshead speed is 50 mm / min.
  • a simultaneous friction is imposed on 15 stationary wires, the tension of which is kept constant at 15 wires by 3 brass rollers ensuring interlocking.
  • the point of application of the lashing area is moved along the wires over an amplitude of 90 mm at a frequency of 220 cycles per minute.
  • Abrasion resistance is defined by the number of cycles (back and forth) required to break 13 of the 15 wires. The measurements presented are the average of the values obtained on three tests with similar wires.
  • the characteristics of the yarns produced are presented in Table 2.
  • the properties measured are presented in Table 3.
  • Examples 15-17 Compositions comprising platelet particles based on zirconium phosphate.
  • a polyamide 6 is synthesized from caprolactam according to a conventional process, by introducing into the polymerization medium an aqueous dispersion obtained in Example 4.
  • the proportion of compound based on zirconium phosphate introduced is 1 (Example 16) or 2 (example 17)% by weight.
  • a polymer is also synthesized that does not contain the compound (Example 15, comparative).
  • the polymer After polymerization, the polymer is formed into granules. These are washed to remove the residual caprolactam (the granules are immersed in an excess of water at
  • HDT-Heat Deflection Temperature HDT-Heat Deflection Temperature
  • Polyamide-based compositions are obtained whose tensile strength, modulus and deformation temperature under load are higher than those of a polyamide not comprising the mineral compound.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Inorganic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Paper (AREA)
EP01965341A 2000-08-23 2001-08-23 Composes mineraux, leur procede de preparation et leur utilisation dans les materiaux thermoplastiques Withdrawn EP1349807A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR0010872A FR2813300B1 (fr) 2000-08-23 2000-08-23 Procede de preparation de composes mineraux, composes obtenus, et leur utilisation dans les materiaux thermoplastiques
FR0010872 2000-08-23
PCT/FR2001/002653 WO2002016264A1 (fr) 2000-08-23 2001-08-23 Composes mineraux, leur procede de preparation et leur utilisation dans les materiaux thermoplastiques

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EP1349807A1 true EP1349807A1 (fr) 2003-10-08

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US (1) US7241827B2 (pt)
EP (1) EP1349807A1 (pt)
JP (1) JP2004506585A (pt)
KR (1) KR100639290B1 (pt)
AU (1) AU2001286002A1 (pt)
BR (1) BR0113434A (pt)
CA (1) CA2420323A1 (pt)
FR (1) FR2813300B1 (pt)
MX (1) MXPA03001583A (pt)
WO (1) WO2002016264A1 (pt)

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JP4857471B2 (ja) * 2001-02-06 2012-01-18 株式会社豊田中央研究所 多孔性物質及びその製造方法、並びにそれを用いた触媒
FR2836476B1 (fr) * 2002-02-22 2005-03-18 Rhodianyl Materiau thermoplastique a proprietes barrieres elevees
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AU2001286002A1 (en) 2002-03-04
MXPA03001583A (es) 2004-11-01
JP2004506585A (ja) 2004-03-04
US20040033186A1 (en) 2004-02-19
KR100639290B1 (ko) 2006-10-27
BR0113434A (pt) 2003-06-24
FR2813300A1 (fr) 2002-03-01
WO2002016264A1 (fr) 2002-02-28
FR2813300B1 (fr) 2002-10-25
US7241827B2 (en) 2007-07-10
KR20030053505A (ko) 2003-06-28

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