WO1995028716A1 - Matiere electroconductrice et procede de preparation - Google Patents

Matiere electroconductrice et procede de preparation Download PDF

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Publication number
WO1995028716A1
WO1995028716A1 PCT/FI1995/000085 FI9500085W WO9528716A1 WO 1995028716 A1 WO1995028716 A1 WO 1995028716A1 FI 9500085 W FI9500085 W FI 9500085W WO 9528716 A1 WO9528716 A1 WO 9528716A1
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WIPO (PCT)
Prior art keywords
dry blend
polyaniline
blend
dry
complex
Prior art date
Application number
PCT/FI1995/000085
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English (en)
Inventor
Esa Karhu
Toivo Kärnä
Jukka Laakso
Matti Suominen
Matti Jussila
Pauli Kirmanen
Original Assignee
Neste Oy
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 Neste Oy filed Critical Neste Oy
Priority to AU17096/95A priority Critical patent/AU1709695A/en
Priority to EP95908969A priority patent/EP0756748A1/fr
Publication of WO1995028716A1 publication Critical patent/WO1995028716A1/fr

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Classifications

    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
    • H01B1/12—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
    • H01B1/124—Intrinsically conductive polymers
    • H01B1/128—Intrinsically conductive polymers comprising six-membered aromatic rings in the main chain, e.g. polyanilines, polyphenylenes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/02—Polyamines
    • C08G73/026—Wholly aromatic polyamines
    • C08G73/0266—Polyanilines or derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10—Homopolymers or copolymers of propene
    • C08L23/12—Polypropene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02—Homopolymers or copolymers of hydrocarbons
    • C08L25/04—Homopolymers or copolymers of styrene
    • C08L25/06—Polystyrene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00

Definitions

  • the invention relates to an electrically conductive plastics blend which contains a polyaniline complex doped with a protonic acid and which is prepared by dry mixing an electrically conductive polyaniline complex and a matrix plastic.
  • the invention also relates to a method for preparing such an electrically conductive dry blend.
  • the blend thus obtained may be processed further into desired end products by using conventional plastics processing methods.
  • Electrically conductive plastics blends in which the conductive component is an intrinsical ⁇ ly conductive polymer can be prepared according to the state of the art by mixing in molten state an electrically conductive polymer and a matrix plastic.
  • the electrically conductive components used may also be various other conductive particles, for example carbon black, metals, and various powders and fibers, such as carbon fibers.
  • Typical electrically conductive plastics products include various films, coatings such as plastic floor coverings, sheets, pipes, various formed pieces, etc.
  • the most common areas of use include various targets requiring EMI and ESD shielding, for example in the packaging industry, the electronics industry, the coating of spaces requiring shielding, etc.
  • Intrinsically conductive polymers are produced by adding to polymers suitable oxidizing or reducing agents, i.e. dopants. These serve in the polymer as electron acceptors or electron donors, whereby electron holes or excess electrons are formed in the polymer, enabling electric current to travel along the conjugated chain.
  • suitable oxidizing or reducing agents i.e. dopants. These serve in the polymer as electron acceptors or electron donors, whereby electron holes or excess electrons are formed in the polymer, enabling electric current to travel along the conjugated chain.
  • suitable oxidizing or reducing agents i.e. dopants.
  • dopants serve in the polymer as electron acceptors or electron donors, whereby electron holes or excess electrons are formed in the polymer, enabling electric current to travel along the conjugated chain.
  • mtrinsically conductive polymers known in the art include poly acetylene, poly-p-phenylene, poly- pyrrole, polythiophene with its derivatives, and polyaniline
  • Polyaniline with its derivatives has proved to be a technically and commercially promising electrically conductive polymer.
  • Polyaniline may be present in a number of forms, which include leucoemeraldine, protoemeraldine, emeraldine, nigraline and toluprotoemeraldine forms.
  • Polyaniline can be rendered electrically conductive by being doped with a protonic acid, such as protonic mineral acids or organic acids. Examples of doping acids used include HC1, H 2 S0 4 , HN0 3 , HCIO 4 , HBF 4 , HPF 6 , HF, phosphoric acids, sulfonic acids, picrinic acid, n-nitrobenzoic acid, dichloroacetic acid, and polymeric acids.
  • the doping is carried out using sulfonic acid or its derivatives, and dodecylbenzenesulfonic acid (DBSA) has proved to be the most preferable doping acid.
  • DBSA dodecylbenzenesulfonic acid
  • such a doped polyaniline is as such a staining or corrosive liquid or viscous material which is difficult to handle.
  • EP patent publication 545 729 discloses a method for bringing a polyaniline doped with a protonic acid to an easy-to-handle, melt-processible form by heat treating it with sulfonic acid or its derivative at a temperature of approx. 40 °C - 250 °C.
  • EP patent publication 582919 further discloses a method by which it is possible to produce an electrically conductive, melt-processible polyaniline complex which has a substantially neutral pH and is easy to handle.
  • a metal compound most preferably zinc oxide
  • plasticizing the polyaniline plasticizing the polyaniline.
  • plasticization is meant the rendering of the polymer such that it can be further processed to the desired form for application.
  • An electrically conductive, melt-processible polyaniline complex, having a substantially neutral pH, prepared by the methods described above, can be mixed, as is also stated in the above-mentioned publications, by conventional melt-mixing methods with any matrix plastics generally used for this purpose.
  • the most common matrix plastics include homo- or copolymers based on, for example, olef ⁇ ns, styrene, vinyl polymers or acrylic poly ⁇ mers, or their mixtures or thermoplastic condensation polymers.
  • Some of the most commonly used matrix polymers include polyethylene, polypropylene, styrene butadiene, polystyrene, polyvinyl chloride, polyamide, and polyester.
  • the proportion mentioned for the conductive polymer complex in such plastics blends prepared by melt-mixing methods is 1-50 % by weight, preferably 1-25 % by weight, and most preferably 5-15 % by weight.
  • such plastics blends should, however, in general contain the conductive polymer complex at least in an amount of 5 % by weight; most often the amount of the complex is at a level of approx. 10 % by weight.
  • the electrically conductive plastics blends contain, depending on the matrix polymer and the targeted use, for example softeners, stabilizers, pigments, mold lubricants, modifiers, and fillers.
  • softeners for example in PNC products, are derivatives of phthalic acids, such as phthalates, of which the most commonly used is dioctyl phthalate (DOP).
  • DOP dioctyl phthalate
  • the stabilizers are most commonly metal soaps, inorganic acids (such as barium and lead salts), organostannium compounds, and epoxy compounds. Both organic and inorganic pigments and dyes can be used as coloring agents.
  • the mold lubricants may be, for example, long-chain alcohols or various waxes.
  • Plastics blends containing a conductive polyaniline complex as described above are thus prepared, as stated above, by a melt mixing method.
  • the processibility of the electrically conductive, protonic acid doped and plasticized polyanili ⁇ ne complex present in the plastics blends is limited with respect to the common plastics processing temperatures and methods. Problems may appear in both the structural stability and the stability of the electrical conductivity of the polyaniline complex. Since in the polymer melt-mixing step the temperature must be raised above the thermal resistance limit of the doped polyaniline complex, destruction of the polymer blend will follow within a very short time. For example, the typical processing temperature of PNC is within the range 165 °C - 180 °C.
  • plastics blend additives such as pigments, stabilizers, plasticizers, and lubricants.
  • a product so prepared is a material which produces dust, is difficult to handle, and is non-homogenous.
  • separation of the various components, i.e. the conductive particles and the matrix polymer particles will occur in it, and as a result the material will have an unevenly distributed conductivity, which in turn will cause the processed end product to be uneven in quality.
  • electrically conductive plastics blends can also be prepared by using dry- mixing techniques, known per se.
  • the conductive component used is carbon black, metals, various powders, and fibers, such as carbon fibers.
  • the use of such components causes, for example, problems associated with the outer appearance of the product (e.g. color problems), mechanical and technical problems, and problems associated with the control of the conductivity level.
  • Intrinsically conductive polymers have not previously been used in such blends prepared by dry-mixing techniques.
  • dry mixing is meant the mixing of the components with each other in high-speed mixers, which include friction mixers, which typically have a cooling mantle by means of which excessive elevation of the temperature during mixing can be prevented.
  • Examples of the use of carbon black in the form of a softener dispersion in a PNC matrix include US patent publications 4 976 890 and 5 066 422. In the methods described in these publications, a preliminary blend (softener, carbon black and stabilizers) is com ⁇ bined with a porous PVC resin. The temperature in the mixing step must not rise above 70 °C.
  • composition disclosed in EP patent publication 539 936 comprises a thermoplastic polymer and, as the conductive material, a short fiber derived from carbon or germanium. These can be combined by dry mixing or by compounding the mixture in, for example, an extruder.
  • US patent publication 5 217 649 discloses a plastics blend in which the conductive polymer, such as polyaniline, is dispersed in a matrix plastic which contains a sulfonamide softener. What is in question is thus not a dry blend of an electrically conductive polymer and a matrix plastic.
  • US patent publication 5 254 633 discloses a process for the preparation of a plastics blend, in which process matrix polymer particles and conductive polymer particles are contacted with each other by means of a medium which serves as a solvent. This medium must subsequently be removed from the blend, for example by evaporation, before the further processing of the blend.
  • EP patent publication 497 514 discloses a blend of PNC, doped polyaniline, a softener, and additives, the blend being formed by dispersing polyaniline into PVC in a 2-roll mill. According to the publication, highly polar, ester-free softeners, such as sulfonamides, must be used as the softener, since, according to the publication, polyaniline reacts with conventional softeners, such as esters, used with PNC, thus causing a weakening of the conductivity.
  • EP patent publication 500 054 further discloses a dry blend of two resins and a process for its preparation, the purpose being to produce a carrier for a two-component developing agent for the developing of electrostatic latent pictures.
  • seed particles formed of ferromagnetic metals and alloys, as well as a fluorine-containing resin and a resin having a lower melting point than the first- mentioned resin are dry mixed together, and the mixture is heated while stirring so that the coating resin, having a lower melting point, will soften and melt and coat the seed particles with a continuous coating layer. This is followed by a cooling to prevent agglomeration of the carrier particles.
  • This publication does not describe the use of a conductive polymer in the blend.
  • a further example of dry mixing is US patent publication 4 889 673, which describes a dry-mixing process for a suspension PNC to be used for extrusion molding, a softener, stabilizer and pigments by using a mixer having a high shear force.
  • the temperature during mixing is maintained below 165 °C, preferably the mixing temperature is 80 °C - 110 °C, i.e. the temperature must be well below the melting temperature of PNC, which is 170 °C.
  • the blend thus obtained is kneaded and pelleted by extrusion.
  • the process according to this publication includes neither the use of conductive particles in the preparation of the blend nor the mixing of different polymers with each other.
  • the polyaniline is dispersed in the matrix, and no results regarding this dispersion remaining a homogenous material are disclosed. Furthermore, it is important to note that no pH values of the polyaniline-matrix dispersion are presented, and it can be assumed that they are acid compositions. The polyaniline used in these blends it not a doped and plasticized, substantially neutral polyaniline.
  • An object of the present invention is thus to provide an electrically well conductive plastics blend prepared by dry-mixing techniques, in which blend the conductive com ⁇ ponent is a polyaniline complex doped with a protonic acid and containing a plasticizing agent, and the matrix polymer consists of one or several commonly used matrix plastics, and which blend is suitable for being further processed by conventional plastics processing methods.
  • Another object of the invention is a plastics blend in which better electrical conductivities are achieved with a lower content of conductive polymer and in which the conductivity withstands the processing of the blend into the desired end products.
  • the mixing together of a matrix polymer and a conductive polymer complex may, instead of compounding in molten state, be conducted by dry mixing the components with each other in a dry mixer the temperature of which can be adjusted and by selecting a suitable plasticizer for the polyaniline.
  • the mixing must be carried out at so low a temperature that thermal decomposition of the polymer will not occur, but at such a temperature that a dry blend according to the invention, having the properties stated above, will be formed. This can be done by selecting a suitable com ⁇ pound which plasticizes the doped polyaniline.
  • An electrically conductive dry blend which contains a protonic acid doped polyaniline and a matrix polymer/matrix polymers is thus characterized in what is stated in the characterizing clause of Claim 1.
  • the preparation of an electrically conductive dry blend according to the invention is thus based on the fact that, when the plasticizer melts on the complex particle during mixing, the temperature being below 125 °C, preferably below 120 °C, the complex particle easily adheres to the surface of a matrix polymer particle, and thereby a dust-free dry plastics blend which is easy to handle is produced. Furthermore, separation of matrix polymer particles and complex particles, due to a weight and size difference, is prevented. It can be said that the molten plasticizer serves as if as a "glue" between the complex particles and the matrix polymer particles in the blend. It is important that the plasticizer is selected so that its melting temperature is so low that thermal decomposition of the polymer will not occur.
  • the compound used as the plasticizer must thus be a compound which is capable of plasticizing the conductive polyaniline at a temperature lower than the plasticization temperature of the matrix polymer.
  • the plasticization temperatures of the polymer complex and the matrix polymer are very close to each other, i.e. the differences are below an order of 10 °C, the conse ⁇ quence is that the conductive polymer complex and the matrix polymer will blend physico- chemically with each other, the result not being a dry blend.
  • a dry blend according to the invention is thus prepared at a temperature at which thermal decomposition of the conductive polyaniline does not occur but at which its plasticization can take place. These requirements are fulfilled when the mixing takes place at a tempera ⁇ ture below 125 °C, preferably below 120 °C, but above 80 °C.
  • the lower limit for the temperature is, of course, determined by the melting range of the plasticizer.
  • Suitable plasticizers, which melt and plasticize the polyaniline in a complex at a temperature below 120 °C and by means of which the desired properties of a plastics blend, stated earlier in this specification, are accomplished include sulfonic acid derivatives, most preferably dodecylbenzenesulfonic acid, together with a zinc compound, preferably zinc oxide.
  • the melting properties of the plasticizer are exploited, which further affect the plasticization of the polymer.
  • the plas ⁇ ticization can also be described by the viscosity difference of the polymers so that the plasticized polymer complex has a lower viscosity than has the matrix polymer.
  • the mixing of the conductive polymer complex and the matrix polymer is preferably carried out in high-speed mixers, one such mixer being the so-called friction mixer, in which the temperature rises during mixing but excessive rising of its temperature can be prevented by means of a cooling mantle in the mixer.
  • the matrix polymer particles and the polyaniline complex particles may be: a) of equal size b) the matrix polymer particles larger than the complex particles or c) the matrix polymer particles smaller than the complex particles.
  • the particles are evenly mixed in the dry blend.
  • the complex particles coat the matrix polymer particles, and in case c) the matrix polymer particles for their part coat the complex particles.
  • An improvement of the homogeneity of the blend is thus a significant advantage in the process according to the invention,
  • An advantageous conductivity network structure is already formed in a dry blend prepared according to the invention, and this structure will not substantially change in conventional processing screws designed for the melting and homogenization of plastics.
  • This blend homogeneity, with respect to the structure and thus also the conductivity, is also retained during, for example, transport and storage, since separation of the particles from each other will not occur.
  • the electrically conductive dry blend material is made especially advantageous from the viewpoint of the onward user by the fact that any necessary additives and also a matrix polymer can be added to it, depending on the end products.
  • the dry blend can be regarded as if it were a "concentrate" with which it is possible to mix, i.e. which is capable of binding to itself, other necessary ingredients.
  • the performer of the processing can thus add to this dry blend material, depending on the intended use, a necessary amount of a matrix polymer, such as polyolef ⁇ ns or PNC for example in the form of plastic granulates or powder, softeners, stabilizers, pigments, and other desired additives.
  • the additives may be added to the blend either during its preparation or to the completed blend.
  • Such a dry blend material according to the present invention is, from the viewpoint of not only the supplier of the blend but also the onward user, very practical in terms of the production of an electrically conductive plastics material, its further delivery, and its use for various processing applications.
  • the polyaniline doped with a protonic acid, used in a plastics blend according to the invention, prepared by dry mixing techniques is plasticized and heat treated at a tempera ⁇ ture of 40 °C - 300 °C, preferably 60 °C - 250 °C.
  • the doping protonic acid may be, as stated, a mineral acid or an organic acid.
  • Dodecylbenzenesulfonic acid is a commonly used doping acid.
  • the plasticizer used must thus melt at a temperature below 120 °C.
  • Such a compound is most preferably a compound formed by DBSA and zinc oxide ZnO.
  • a Zn-DBSA compound melts at approx.
  • a Zn-DBSA compound When softening and melting, a Zn-DBSA compound will cause the conductive polyaniline complex particles to adhere during dry mixing to the surfaces of matrix polymer particles, and thus the result will be a dust-free, homogenous, highly electrically conductive plastics blend material which retains its homogeneity well.
  • the plasticized, electrically conductive polyaniline complex used in a dry blend material according to the present invention may have a pH value ranging from acid to nearly neutral. It is, however, usually more advantageous considering the various processing and other apparatus coming into contact with the electrically conductive polyaniline complex that the pH of the complex is substantially within the neutral range. By this is meant in this context a pH range of approx. 3.5 - 7. Preferably the pH value is within the range 4 - 6.5.
  • a plastics dry blend according to the present invention containing an electrically conductive polyaniline complex, is prepared by using the dry-blending techniques known per se.
  • An electrically conductive polyaniline complex which contains the plasticizer is first ground using a shear-action mill to a finely-divided powder.
  • the screen used may be, for example, a screen of 0.5 - 1.5 mm.
  • the molar ratio of the plasticizer to the doped polyaniline may vary within a range of approx. 1 : 0.1 - 1 : 3, preferably within the range 1 : 0.25 - 1 : 1, and most preferably within the range 1 : 0.5 - 1 : 0.7.
  • the polyaniline complex typically contains plasticizer approx. 10 - 50 % by weight and doped polyaniline approx. 90 - 50 % by weight, preferably plastizer approx. 20 - 40 % by weight and doped polyaniline approx. 80 - 60 % by weight.
  • the amount of plasticizer affects not only the result of the plasticization but also the acidity of the polyaniline complex.
  • the plasticized polyaniline complex is mixed with the matrix plastic in a high-speed mixer, such as a friction mixer, at a temperature below 125 °C, preferably below 120 °C.
  • a high-speed mixer such as a friction mixer
  • the mixing time is approx. 10 - 30 min.
  • the proportion of matrix polymer may vary within a wide range, i.e. approx. 99 - 50 % by weight, depending on the desired conductivity level and on the additives added at this stage.
  • the result obtained is a homogenous, electrically well conductive, easy-to-handle dust-free plastics dry blend which retains its conductivity and homogeneity, the acidity of which can be adjusted, and which can be further processed into the desired end products.
  • More matrix plastic or matrix plastics and desired additives can be further mixed with the conductive dry blend obtained from the step described above.
  • the matrix plastic may be in pulverous or granulate form, the pulverous form being, however, generally preferable.
  • the essential point is that a dry blend material is obtained which adapts flexibly to the needs of the onward user.
  • the conductivity level attained with a smaller conductive polymer content in the plastics dry blend material according to the invention is significantly better than that in a product prepared by a conventional melt-mixing method.
  • the achieved conductivity level is preferably at a level > 10 "9 S/cm, preferably at a level > 10 "6 S/cm, and most preferably at a level > 10 *3 S/cm.
  • ESD electrical conductivity
  • conductivities are achieved which better than prior art make EMI and microwave applications possible.
  • pieces made from a dry blend according to the invention have a good attenuation capacity, which property can be exploited, for example, in the manufacture of shielding casings of sensitive electronic devices, such as computers.
  • the antistatic properties of products made from the dry blend can, for their part, be exploited, for example, in transportation and packaging cases for electronic equipment, floor covering applications, etc.
  • the suitable electrical conductivity is at a level of 10 6 - 10 8 ⁇ .
  • a typical floor covering material com ⁇ position may in the main contain, for example, in total 10 % a blend which contains 30 % a Zn-DBSA compound and 70 % doped polyaniline, and 90 % a mixture which contains approx. 50 % PVC and 50 % filler.
  • pieces injection molded from a plastics dry blend according to the invention have moderate and highly comparable mechanical properties as compared with pieces made from a melt-mixed blend.
  • FIG. 1 An enlarged detail of a PVC particle with polyaniline-DBSA complex particles adhering to its surface.
  • Figure 3 A microscopic picture of a polyaniline-DBSA complex particle with PVC particles adhering to its surface.
  • Figure 4 A microscopic picture of PVC particles with polyaniline-DBSA complex particles adhering to their surfaces.
  • Figure 5 depicts the shielding efficiency, i.e. the attenuation capacity (in decibels dB), of a piece injection molded from a dry blend prepared according to Example 1, as a function of the frequency of the incident radiation. It can be seen from the figure that the shielding efficiency drops by approx. 20 dB when the frequency increases by one order, from the 5th exponential to the 6th exponential, but remains unchanged thereafter up to the 8th exponential.
  • the shielding efficiency i.e. the attenuation capacity (in decibels dB)
  • An electrically conductive, solidified polyaniline complex was prepared in which the proportion of polyaniline doped with dodecylbenzenesulfonic acid (DBSA) was 60 % by weight and the proportion of the Zn-DBSA compound used as the plasticizer was 40 % by weight.
  • DBSA dodecylbenzenesulfonic acid
  • This complex was mixed with the polypropylene powder (VB 6550B, manufacturer Neste Oy) used as the matrix polymer and with Ketjenflex 9S sulfonamide additive at the weight ratio 47.5 : 47.5 : 5 in a friction mixer (Henschel FM10L). The mixing time was 16 minutes and the temperature was at maximum 125 °C. The mixture was cooled for 15 minutes while mixing was continued. The size of the batch mixed was 1000 g.
  • a master batch dry blend prepared in accordance with Example 1 was further mixed by dry-mixing the homopolymer with the polypropylene VB 6550B at different ratios. Round pieces were formed from the blend in an injection mold KM210. Table 1 shows the master batch contents, complex contents, and the contents of the added polypropylene in the blends prepared.
  • Reference samples 5 samples were prepared, in which the doped polyaniline complex was mixed directly with the matrix polymer VB 6550B by the melt-mixing method in an injection mold and was processed into test sheets. The absorption capacity of the sheets per wavelength, i.e. their attenuation coefficient tan( ⁇ ) at the frequency 11 GHz, was measured. The contents of the complex and the matrix polymer and the obtained attenuation coefficients are shown in Table 3. The reference samples are indicated by the code MaK 1-5.
  • Blends 1. PVC 100 phr, DOP 15 phr, and complex 30 phr
  • Example 5 30 phr of polyaniline complex Cl/9 EB96 A70B30, which had been milled in a disinte ⁇ grator, 100 phr of PVC S88Y, and 10 phr of DOP were mixed as in Example 5.
  • a microscopic picture, Figure 3 was taken of the dry blend. The figure shows that the obtained dry blend consists of PVC particles with polyaniline-DBSA complex particles adhering to their surfaces. The particles are of an even quality and the formed blend is homogenous.
  • Example 6 With the mixing proportions and mixing method according to Example 6, a dry blend was prepared on an industrial scale (an approx. 100 kg batch) by using a blend con ⁇ taining 30 phr of polyaniline complex, 100 phr of PVC, and 10 phr of DOP.
  • the dry blend thus obtained was highly homogenous, it did not produce any dust, and the dry blend was easy to batch.
  • PVC floor covering was made from the dry blend. The outer appearance of the floor covering was good and even.
  • the electrical conductivity measu- red of the floor covering was in accordance with the standard.
  • the electrical conducti ⁇ vities of floor coverings made from the dry blend were more even and better controlla ⁇ ble than those of floor coverings made by conventional methods.
  • Example 8
  • Two blends were prepared, each having the same ingredients as follows: 51 g of so- called floor covering mix (contains the PVC, stabilizers, etc.), 8 g of a polyaniline complex containing a Zn-DBSA plasticizer, 3 g of TiO 2 , and 3 g of a color pigment.
  • the first blend was prepared using a known melt-mixing method, and the second blend was prepared using the dry-mixing method according to the invention. Electrical con ⁇ ductivities were measured from the obtained blends. The result was that the electrical conductivity of the blend obtained by the melt-mixing method was 5 M ⁇ , whereas that of the blend obtained by the dry-mixing method was, repeatedly measured, as high as 40 k ⁇ .
  • the difference in electrical conductivity between the blend prepared by the melt-mixing method and the dry blend according to the invention is thus highly signifi ⁇ cant - the differences are up to several decades in favor of the dry blend according to the invention.
  • the plastics dry blend according to the invention is, with respect to its technical properties, handlability, outer appearance, and processibility, a material highly practical and usable as a raw material for industry using conductive polymer materials.

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Abstract

L'invention se rapporte à des mélanges de matières plastiques électroconducteurs contenant un complexe de polyaniline dopé d'un acide protonique. On prépare ces mélanges en combinant à sec un complexe de polyaniline électroconducteur et une matière plastique formant matrice. Le mélange sec selon l'invention est une matière homogène qui peut être traitée à chaud, et présentant de très bonnes propriétés de conduction électrique, même à de faibles teneurs en polymères conducteurs. L'invention se rapporte également à un procédé de préparation d'un tel mélange sec. Il est possible d'ajouter au mélange davantage de matière plastique formant matrice ainsi que tout additif plastique requis, et de mettre en oeuvre le mélange selon des procédés de traitement de matières plastiques classiques pour obtenir les produits finis requis. Les produits finis préférés sont notamment des enveloppes de blindage, des boîtes d'emballage et des boîtes de transport pour des dispositifs électroniques sensibles, ainsi que différents matériaux de revêtement de sol.
PCT/FI1995/000085 1994-04-18 1995-02-20 Matiere electroconductrice et procede de preparation WO1995028716A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
AU17096/95A AU1709695A (en) 1994-04-18 1995-02-20 Electrically conducting material and a method to prepare it
EP95908969A EP0756748A1 (fr) 1994-04-18 1995-02-20 Matiere electroconductrice et procede de preparation

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FI941783 1994-04-18
FI941783A FI102683B1 (fi) 1994-04-18 1994-04-18 Sähköä johtava kuivasekoite ja menetelmä sen valmistamiseksi

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WO1995028716A1 true WO1995028716A1 (fr) 1995-10-26

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AU (1) AU1709695A (fr)
FI (1) FI102683B1 (fr)
WO (1) WO1995028716A1 (fr)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0782970A1 (fr) * 1995-12-26 1997-07-09 Morita, Ken-ichi Agents et méthode de génération d'oxygène actif
FR2751660A1 (fr) * 1996-07-29 1998-01-30 Commissariat Energie Atomique Composition pour la fabrication d'un materiau composite conducteur contenant une polyaniline et materiau composite obtenu a partir de cette composition
US5741887A (en) * 1995-12-26 1998-04-21 Ken-ichi Morita Agents and methods for generation of active oxygen
FR2783524A1 (fr) * 1998-09-22 2000-03-24 Commissariat Energie Atomique Materiau a resistance au vieillissement thermique amelioree et son procede de fabrication
CN106750918A (zh) * 2016-12-08 2017-05-31 广东美的环境电器制造有限公司 防尘抗污塑料及其制备方法和应用以及防尘电风扇扇叶和防尘电风扇
CN110358194A (zh) * 2019-08-22 2019-10-22 苏州润佳工程塑料股份有限公司 一种抗静电聚丙烯复合材料及其制备方法
CN116218081A (zh) * 2023-03-23 2023-06-06 江苏金发科技新材料有限公司 一种聚丙烯复合材料及其制备方法

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0582919A2 (fr) * 1992-08-11 1994-02-16 Neste Oy Matériau de plastique conducteur et méthode de sa préparation

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0582919A2 (fr) * 1992-08-11 1994-02-16 Neste Oy Matériau de plastique conducteur et méthode de sa préparation

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0782970A1 (fr) * 1995-12-26 1997-07-09 Morita, Ken-ichi Agents et méthode de génération d'oxygène actif
US5741887A (en) * 1995-12-26 1998-04-21 Ken-ichi Morita Agents and methods for generation of active oxygen
US6235220B1 (en) 1996-01-29 2001-05-22 Commissariat A L'energie Atomique Composition for producing a conductive composite material containing a polyaniline, and resulting composite material
FR2751660A1 (fr) * 1996-07-29 1998-01-30 Commissariat Energie Atomique Composition pour la fabrication d'un materiau composite conducteur contenant une polyaniline et materiau composite obtenu a partir de cette composition
WO1998005040A1 (fr) * 1996-07-29 1998-02-05 Commissariat A L'energie Atomique Composition pour la fabrication d'un materiau composite conducteur contenant une polyaniline et materiau composite obtenu a partir de cette composition
FR2783524A1 (fr) * 1998-09-22 2000-03-24 Commissariat Energie Atomique Materiau a resistance au vieillissement thermique amelioree et son procede de fabrication
WO2000017274A1 (fr) * 1998-09-22 2000-03-30 Commissariat A L'energie Atomique Materiau a resistance au vieillissement thermique amelioree et son procede de fabrication
CN106750918A (zh) * 2016-12-08 2017-05-31 广东美的环境电器制造有限公司 防尘抗污塑料及其制备方法和应用以及防尘电风扇扇叶和防尘电风扇
CN110358194A (zh) * 2019-08-22 2019-10-22 苏州润佳工程塑料股份有限公司 一种抗静电聚丙烯复合材料及其制备方法
CN110358194B (zh) * 2019-08-22 2022-04-01 苏州润佳工程塑料股份有限公司 一种抗静电聚丙烯复合材料及其制备方法
CN116218081A (zh) * 2023-03-23 2023-06-06 江苏金发科技新材料有限公司 一种聚丙烯复合材料及其制备方法

Also Published As

Publication number Publication date
FI941783A0 (fi) 1994-04-18
EP0756748A1 (fr) 1997-02-05
FI941783A (fi) 1995-10-19
AU1709695A (en) 1995-11-10
FI102683B (fi) 1999-01-29
FI102683B1 (fi) 1999-01-29

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