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WO2006066394A1 - Melanges maitres de caoutchouc - Google Patents

Melanges maitres de caoutchouc Download PDF

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Publication number
WO2006066394A1
WO2006066394A1 PCT/CA2005/001887 CA2005001887W WO2006066394A1 WO 2006066394 A1 WO2006066394 A1 WO 2006066394A1 CA 2005001887 W CA2005001887 W CA 2005001887W WO 2006066394 A1 WO2006066394 A1 WO 2006066394A1
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WO
WIPO (PCT)
Prior art keywords
olefin
vinyl acetate
rubber
polymer
gel content
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.)
Ceased
Application number
PCT/CA2005/001887
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English (en)
Inventor
Richard Pazur
Werner Obrecht
Bill Best
Lorenzo Ferrari
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.)
Arlanxeo Canada Inc
Original Assignee
Lanxess Inc
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Filing date
Publication date
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Publication of WO2006066394A1 publication Critical patent/WO2006066394A1/fr
Anticipated expiration legal-status Critical
Ceased 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
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L15/00—Compositions of rubber derivatives
    • C08L15/005—Hydrogenated nitrile rubber
    • 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
    • C08L23/04—Homopolymers or copolymers of ethene
    • C08L23/08—Copolymers of ethene
    • C08L23/0846—Copolymers of ethene with unsaturated hydrocarbons containing atoms other than carbon or hydrogen
    • C08L23/0853—Ethene vinyl acetate copolymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L31/00—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 acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid; Compositions of derivatives of such polymers
    • C08L31/02—Homopolymers or copolymers of esters of monocarboxylic acids
    • C08L31/04—Homopolymers or copolymers of vinyl acetate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/14—Peroxides
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00—Polymer mixtures characterised by other features
    • C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00—Polymer mixtures characterised by other features
    • C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L35/00—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 a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L35/04—Homopolymers or copolymers of nitriles

Definitions

  • the present invention relates to a rubber masterbatch containing at least one hydrogenated nitrile polymer, at least two olefin/vinylacetate and/or olefin/acrylate polymers and at least one processing aid, wherein at least one of the olefin/vinyl acetate and/or olefin/acrylate polymers is precrosslinked.
  • the present invention also relates to a curable rubber compound containing the rubber masterbatch and at least one vulcanization agent and at least one filler. Further, the present invention relates to a shaped article containing the curable rubber compound.
  • Hydrogenated nitrile rubbers prepared by the selective hydrogenation of nitrile rubber (NBR, a co-polymer comprising at least one conjugated diene, at least one unsaturated nitrile and optionally further comonomers) are specialty rubbers which have very good heat resistance, excellent ozone and chemical resistance, and excellent oil resistance.
  • HNBR high level of mechanical properties of the rubber
  • oil stators, well head seals, valve plates
  • electrical electrical
  • mechanical engineering wheels, rollers
  • shipbuilding pipe seals, couplings
  • HNBR's that have good low temperature properties.
  • Therban ® LT 2157 is a terpolymer, available from Lanxess, composed of 21 wt% acrylonitrile, acrylate, and butadiene, that has a residual double bond content (RDB) of 5.5% and a glass transition temperature (Tg) of -38° C.
  • Therban ® LT VP KA 8882 is similar, but differs in having an RDB of less than 0.9%, and, again, has a Tg of -38.° C.
  • WO-02/16441 -A discloses a hydrogenated copolymer of an unsaturated nitrile, butadiene and isoprene, wherein the molar ratio of butadiene to isoprene is less than 3:1.
  • EP-A-O 151 691 discloses a blend of 95-5 wt.% of EVA and 5-95 wt.% of HNBR.
  • CA 2,436,742 discloses a polymer blend comprising at least one, preferably statistical, hydrogenated nitrile rubber, at least one, preferably statistical, hydrogenated nitrile terpolymer rubber, at least one, preferably binary, salt of a strong base and a weak acid comprising a group 1 metal, and at least one olefin/vinylacetate or olefin/acrylate rubber.
  • the present invention relates to a rubber masterbatch containing (i) at least one, preferably statistical, hydrogenated nitrile polymer, (ii) at least two olefin/vinyl acetate and/or olefin/acrylate polymers, wherein at least one of the olefin/vinyl acetate and/or olefin/acrylate polymers has a gel content and a swelling index which is adjusted with gamma radiation and wherein the radiation adjusted polymer has a gel content of 40 to 80% based on the total mass of the olefin/vinyl acetate and/or olefin/acrylate polymer and a swelling index of 20 to 80 based on the gel, and (iii) at least one processing aid.
  • the present invention also relates to a rubber masterbatch containing (i) at least one, preferably statistical, hydrogenated nitrile terpolymer rubber, (ii) at least two olefin/vinyl acetate and/or olefin/acrylate polymers, wherein at least one of the olefin/vinyl acetate and/or olefin/acrylate polymers has a gel content and a swelling index which is adjusted with gamma radiation and wherein the radiation adjusted polymer has a gel content of 40 to 80% based on the total mass of the olefin/vinyl acetate and/or olefin/acrylate polymer and a swelling index of 30 to 75 based on the gel, and
  • the present invention relates to curable rubber compound containing the rubber masterbatch and at least one filler, and at least one vulcanization agent.
  • the present invention relates to a shaped article containing the curable rubber compound.
  • Rubber compounds containing rubber masterbatches according to the present invention have improved processability due to lower compound Mooney viscosity and quicker Mooney relaxation times compared to rubber compounds conventionally prepared. Also, rubber compounds containing rubber masterbatches according to the present invention have improved physical properties, in particular, higher moduli or overall compound stiffness.
  • nitrile rubber As used throughout this specification, the term "nitrile rubber”, “nitrile polymer” or NBR is intended to have a broad meaning and is meant to encompass a copolymer having repeating units derived from at least one conjugated diene, at least one alpha, beta-unsatu rated nitrile and optionally further copolymerizable monomer(s).
  • nitrile terpolymer rubber or "LT-NBR” is intended to have a broad meaning and is meant to encompass a copolymer having (a) repeating units derived from at least one conjugated diene, (b) at least one alpha, beta-unsaturated nitrile, (c) repeating units derived from at least one further monomer selected from the group consisting of conjugated dienes, unsaturated carboxylic acids; alkyl esters of unsaturated carboxylic acids, alkoxyalkyl acrylates and ethylenically unsaturated monomers other than dienes and (d) optionally further copolymerizable monomer(s).
  • HNBR residual C-C double bonds
  • the conjugated diene may be any known conjugated diene preferably a C 4 - C- 6 conjugated diene.
  • Preferred conjugated dienes include butadiene, isoprene, piperylene, 2,3-dimethyl butadiene and mixtures thereof. Even more preferred C 4 - Ce conjugated dienes include butadiene, isoprene and mixtures thereof. The most preferred C 4 -C ⁇ conjugated diene is butadiene.
  • the alpha, beta-unsatu rated nitrile may be any known alpha, beta- unsaturated nitrile, preferably a C 3 -C 5 alpha, beta-unsaturated nitrile.
  • Preferred C 3 -C 5 alpha, beta-unsaturated nitriles include acrylonitrile, methacrylonitrile, ethacrylonitrile and mixtures thereof.
  • the most preferred C 3 -C 5 alpha, beta- unsaturated nitrile is acrylonitrile.
  • the unsaturated carboxylic acid may be any known unsaturated carboxylic acid copolymerizable with the other monomers, preferably a C 3 -C 16 alpha, beta- unsaturated carboxylic acid.
  • Preferred unsaturated carboxylic acids include acrylic acid, methacrylic acid, itaconic acid and maleic acid and mixtures thereof.
  • the alkyl ester of an unsaturated carboxylic acid may be any known alkyl ester of an unsaturated carboxylic acid copolymerizable with the other monomers, preferably an alkyl ester of an C 3 -C 16 alpha, beta-unsaturated carboxylic acid.
  • Preferred alkyl ester of an unsaturated carboxylic acid include alkyl esters of acrylic acid, methacrylic acid, itaconic acid and maleic acid and mixtures thereof, preferably methyl acrylate, ethylacrylate, butylacrylate, 2-ethylhexyl acrylate and octyl acrylate.
  • alkyl esters include methyl, ethyl, propyl, butyl and octyl esters.
  • the alkoxyalkyl acrylate may be any known alkoxyalkyl acrylate copolymerizable with the other monomers, preferably methoxyethyl acrylate, ethoxyethyl acrylate and methoxyethoxyethyl acrylate and mixtures thereof
  • the ethylenically unsaturated monomer may be any known ethylenically unsaturated monomer copolymerizable with the other monomers, preferably allyl glycidyl ether, vinyl chloroacetate, ethylene, butene-1 , isobutylene and mixtures thereof.
  • the HNBR in the masterbatch according to the present invention contains in the range of from 40 to 85 weight percent of repeating units derived from one or more conjugated dienes and in the range of from 15 to 60 weight percent of repeating units derived from one or more unsaturated nitriles. More preferably, the HNBR contains in the range of from 60 to 75 weight percent of repeating units derived from one or more conjugated dienes and in the range of from 25 to 40 weight percent of repeating units derived from one or more unsaturated nitriles. Most preferably, the HNBR contains in the range of from 60 to 70 weight percent of repeating units derived from one or more conjugated dienes and in the range of from 30 to 40 weight percent of repeating units derived from one or more unsaturated nitriles.
  • the nitrile terpolymer rubber in the masterbatch according to the present invention is a hydrogenated alpha, beta-unsaturated nitrile/ butadiene/isoprene rubber.
  • the ratio of repeating units derived from butadiene to repeating units derived from isoprene is preferably below 3:1 , more preferably below 2:1.
  • the ratio can be as low as 0.1 :1 , but is preferably not less than 0.5:1. Good results are obtained with a ratio of 1 :1 and the preferred range is 0.75:1 to 1 :0.75.
  • the butadiene plus isoprene usually constitutes in the range of from 50 to 95% of the copolymer, and the nitrile usually constitutes in the range of from 5 to 50% of the copolymer.
  • the nitrile content does not normally exceed 36% and is preferably below 30%.
  • the preferred lower limit on the nitrile content is 15%, because copolymers with lower nitrile contents tend to lose their oil resistance. For applications where oil resistance is not of importance, however, lower nitrile contents are acceptable, down to 10% or even 5%. For most purposes a nitrile content of 15 to 25% is preferred.
  • the nitrile terpolymer rubber is a hydrogenated alpha, beta-unsatu rated nitrile/butadiene/acrylate rubber.
  • the combined butadiene and acrylate content constitutes a range of 50 to 95% of the terpolymer, while the nitrile is in the range of 5 to 50%. More preferably, the nitrile range is between 10 and 30%.
  • Commercially available examples of such terpolymers include
  • Therban® LT 2157 (21% nitrile content, 5.5% residual double bonds)
  • Therban® LT VP KA 8882 (21% nitrile content, 0.9 % maximum double bond content).
  • the hydrogenated nitrile polymer and/or the hydrogenated nitrile terpolymer rubber may further contain repeating units derived from one or more copolymerizable monomers. Repeating units derived from one or more copolymerizable monomers will replace either the nitrile or the diene portion of the nitrile rubber and it will be apparent to the skilled in the art that the above mentioned figures will have to be adjusted to result in 100 weight percent.
  • the olefin/vinylacetate polymers in the masterbatch according to the present invention may be any olefin/vinylacetate rubber known in the art.
  • the olefin may be any known olefin, preferably ethylene, propylene, butenes, pentenes, hexenes, heptenes, octenes and their higher homologues and mixtures thereof.
  • the olefin/vinylacetate rubber usually contains in the range of from 10-95 wt.%, preferably 10-80 wt%., of repeating units derived from the olefin monomer(s) and in the range of from 5-90 wt.%, preferably 20-90 wt.%, of repeating units derived from the vinylacetate.
  • the olefin/acrylate polymer may be any olefin/ acrylate rubber known in the art.
  • the olefin may be any known olefin, preferably ethylene, propylene, butenes, pentenes, hexenes, heptenes, octenes and their higher homologues and mixtures thereof.
  • the acrylate may be any known acrylate copolymerizable with the olefin, preferably acrylic acid and derivatives such as methacrylic acid and methylmethacrylate.
  • the olefin/acrylate rubber usually contains in the range of from 5-95 wt.%, preferably 10-80 wt%., of repeating units derived from the olefin monomer(s) and in the range of from 5-95 wt.%, preferably 20-90 wt.%, of repeating units derived from the acrylate(s).
  • At least one of the olefin/vinylacetate and/or olefin/acrylate polymers in the masterbatch according to the present invention is a precrosslinked olefin/vinylacetate and/or a precrosslinked olefin/acrylate polymer prepared according to United States Patent No. 6,399,671 , the contents of which are herein incorporated by reference.
  • the precrosslinked polymers in the masterbatch according to the present invention are those synthesized from ethylene and vinyl acetate, from ethylene and the above-stated acrylates.
  • the mixture ratio of the monomers relative to each other is conventionally 0.1 %-99.9%, preferably 5%-95%, more preferably 30%-80%.
  • the gel content and degree of swelling of the precrosslinked polymers in the masterbatch according to the present invention is established by ionizing radiation.
  • Treatment with ⁇ radiation is preferably considered as the ionizing radiation.
  • the precrosslinked polymers useful in the present invention preferably have a gel content of 30 to 80%, more preferably of 40 to 70%.
  • the swelling index is preferably 20 to 80, more preferably 40 to 60.
  • the gel content and swelling index of the precrosslinked polymers useful in the present invention are determined using the following method: The sample is placed in methylene chloride, to which 1 g/l of lonol had been added, such that there were 12.5 g of polymer per liter of solvent. The mixture is shaken for 6 hours at 14O 0 C, and then centrifuged for 1 hour at 20,000 rpm, wherein the temperature was still maintained at 140 0 C. The sol solution was separated and may optionally be further investigated. The gel is first weighed while moist and the quantity of the dry gel obtained after drying to constant weight in a vacuum drying cabinet is determined.
  • the treatment with ionizing ⁇ radiation is performed at a radiation dose of 20 to 140, preferably of 60 to 120, more preferably of 70 to 100 kGy (kilogray).
  • Irradiation may be performed using any desired plant suitable for this purpose, for example with a 3.5 MCi 60 Co gamma plant (approx. 1.3 MeV).
  • radiation from the 137 Cs isotope is also suitable.
  • the applied radiation dose may, for example, be measured using a photometric system from Far West Technology, USA and the film dosimeter supplied by this company. These film dosimeters contain a radiation-sensitive dye and the radiation dose is calculated on completion of the irradiation process from the change in the absorbance of said dye. These dosimeters are calibrated ex works against an internationally recognized standard.
  • Treatment with ⁇ radiation may be performed in the conventional manner at temperatures of 0° to 130°, preferably of 10° to 120°, more preferably of 20 to 80°C.
  • the most favorable temperature range may readily be determined by appropriate preliminary testing. It is essential that the temperature range is selected such that adequate free radical mobility is ensured.
  • the precrossl inked olefin/vinylacetate and/or olefin/acrylate polymers according to the present invention are preferably produced by initially polymerizing the monomers used in a conventional manner and then treating the resultant polymers with ionizing radiation.
  • the precrosslinked polymers in the most varied forms, ranging from powders to large bales. It must merely be ensured that the ⁇ radiation used sufficiently penetrates the polymers used.
  • suitable apparatus internal mixers, roll mills or co-kneaders. If the precrosslinked polymer is in finely divided form (for example powder or pellets), a powder mixer may also be used for homogenization. By means of this homogenization, it is possible to obtain a product which is entirely uniform with regard to gel content, irrespective of the shape and size of the irradiated container.
  • the desired average gel content may, of course, also be established by blending with non-irradiated or more or less highly irradiated polymers, i.e. with polymers having different gel contents.
  • the amount of the individual polymers and/or rubbers present in the inventive masterbatch may vary in wide ranges and thus it is possible to tailor the properties of the final compound as well as the properties of the final shaped article.
  • the masterbatch contains in the range of from 5 to 50 wt.%, preferably from 10 to 40 wt.%, of at least one, preferably statistical, hydrogenated nitrile rubber and/or in the range of from 5 to 50 wt.%, preferably from 10 to 40 wt.%, of at least one, preferably statistical, hydrogenated nitrile terpolymer rubber , and in the range of from 5 to 50 wt.%, preferably from 10to 40 wt.%, of at least one olefin/vinylacetate rubbers and/or one or more olefin/acrylate rubbers and in the range of from 20 to 80 wt.%, preferably from 30 to 70 wt.%, of at least one precrosslinked olefin/vinylacetate rubbers and/or precrosslinked olefin/acrylate rubbers .
  • the masterbatch according to the present invention further contains at least one processing aid.
  • the masterbatch contain the range of from 0.1 to 5 wt.%, preferably from 0.2 to 1 wt.% of one or more organic fatty acids as an auxiliary product, preferably an unsaturated fatty acid having one, two or more carbon double bonds in the molecule which more preferably includes 10% by weight or more of a conjugated diene acid having at least one conjugated carbon- carbon double bond in its molecule.
  • those fatty acids have in the range of from 8-22 carbon atoms, more preferably 12-18. Examples include stearic acid, palmitic acid and oleic acid and their calcium-, zinc-, magnesium-, potassium- and ammonium salts.
  • the Mooney viscosity of the polymers and/or rubbers in the masterbatch may vary in wide ranges and thus it is possible to tailor the properties of the final compound as well as the properties of the final shaped article.
  • the hydrogenated nitrile polymer and/or hydrogenated nitrile terpolymer may have a Mooney viscosity ML(1 +4@ 100 0 C) of in the range of from 20 to 100 MU, preferably 40 to 80 MU.
  • the olefin/vinyl acetate and/or olefin/acrylate polymer may have a Mooney viscosity ML (1 +4@ 100 0 C) of in the range of from 10 to 90 MU, preferably 20 to 70 MU.
  • the precrosslinked olefin/vinyl acetate and/or olefin/acrylate polymer may have a Mooney viscosity ML (1+4@ 100°C) of in the range of from 30 to 90 MU, preferably 40 to 70 MU.
  • the Mooney viscosity of the raw polymers, the rubber masterbatch and the cured rubber compound containing the inventive masterbatch can be determined using ASTM test D 1646.
  • the present inventive masterbatch may further contain up to 30 wt% of other polymers such as polyolefins, BR
  • the masterbatch according to the present invention is prepared by mixing at least one, preferably statistical, hydrogenated nitrile polymer and/or hydrogenated nitrile terpolymer, at least two olefin/vinyl acetate and/or olefin/acrylate polymers, wherein at least one of the olefin/vinyl acetate and/or olefin/acrylate polymers has a gel content and a swelling index which is adjusted with gamma radiation and wherein the radiation adjusted polymer has a gel content of 40 to 80% based on the total mass of the olefin/vinyl acetate and/or olefin/acrylate polymer and a swelling index of 20 to 80 based on the gel, and at least one processing aid, then compounding the resulting mixture at a temperature in the range of between 75 to 175°C to form a masterbatch.
  • At least one filler and vulcanizing agent has to be added to the masterbatch.
  • Suitable filler(s) may be an active or an inactive filler or a mixture thereof.
  • the filler(s) may be in particular:
  • silicas prepared e.g. by the precipitation of silicate solutions or the flame hydrolysis of silicon halides, with specific surface areas of in the range of from 5 to 1000 m 2 /g, and with primary particle sizes of in the range of from 10 to 400 nm;
  • the silicas can optionally also be present as mixed oxides with other metal oxides such as those of Al, Mg, Ca, Ba, Zn, Zr and Ti;
  • - synthetic silicates such as aluminum silicate and alkaline earth metal silicate like magnesium silicate or calcium silicate, with BET specific surface areas in the range of from 20 to 400 m 2 /g and primary particle diameters in the range of from 10 to 400 nm;
  • - natural silicates such as kaolin and other naturally occurring silica
  • - glass fibers and glass fiber products matting, extrudates or glass microspheres
  • - metal oxides such as zinc oxide, calcium oxide, magnesium oxide and aluminum oxide
  • - metal carbonates such as magnesium carbonate, calcium carbonate and zinc carbonate
  • - metal hydroxides e.g. aluminum hydroxide and magnesium hydroxide
  • the carbon blacks to be used here are prepared by the lamp black, furnace black or gas black process and have preferably BET (DIN 66 131 ) specific surface areas in the range of from 20 to 200 m 2 /g, e.g. SAF, ISAF, HAF, FEF or GPF carbon blacks; - rubber gels, especially those based on polybutadiene, butadiene/styrene copolymers, butadiene/acrylonitrile copolymers and polychloroprene;
  • - large aspect ratio nanoclays such as Cloisite® or mixtures thereof.
  • preferred mineral fillers include silica, silicates, clay such as bentonite, gypsum, alumina, titanium dioxide, talc, mixtures of these, and the like.
  • the preferred mineral is silica, especially silica made by carbon dioxide precipitation of sodium silicate.
  • Dried amorphous silica particles suitable for use in accordance with the invention may have a mean agglomerate particle size in the range of from 1 to 100 microns, preferably between 10 and 50 microns and most preferably between 10 and 25 microns. It is preferred that less than 10 percent by volume of the agglomerate particles are below 5 microns or over 50 microns in size.
  • a suitable amorphous dried silica moreover usually has a BET surface area, measured in accordance with DIN (Deutsche Industrie Norm) 66131 , in the range from 50 and 450 square meters per gram and a DBP absorption, as measured in accordance with DIN 53601 , in the range from 150 and 400 grams per 100 grams of silica, and a drying loss, as measured according to DIN ISO 787/11 , of in the range of from 0 to 10 percent by weight.
  • Suitable silica fillers are available under the trademarks HiSil® 210, HiSil® 233 and HiSil® 243 from PPG industries Inc. Also suitable are Vulkasil® S and Vulkasil® N, from Bayer AG.
  • carbon black is present in the polymer blend in an amount of in the range of from 20 to 200 parts by weight, preferably 30 to 150 parts by weight, more preferably 40 to 100 parts by weight.
  • carbon black and mineral filler in the inventive rubber compound. In this combination the ratio of mineral fillers to carbon black is usually in the range of from 0.05 to 20, preferably 0.1 to 10.
  • the present curable rubber compound containing the inventive masterbatch may further contains a carbodiimide, a polycarbodiimide or mixtures thereof.
  • the preferred carbodiimide is available commercially under the tradenames RhenogranTM PCD-50 and StabaxolTM P.
  • This ingredient may be used in the present curable rubber compound in an amount in the range of from 0 to about 15 parts by weight, more preferably in the range of from 0 to about 10 parts by weight, even more preferably in the range of from about 2 to about 5 parts by weight.
  • the rubber compound containing the inventive masterbatch further comprises at least one vulcanizing agent or curing system.
  • the present invention is not limited to a special curing system; however, peroxide curing system(s) are preferred. Furthermore, the invention is not limited to a special peroxide curing system. For example, inorganic or organic peroxides are suitable.
  • Preferred peroxides include organic peroxides such as dialkylperoxides, ketalperoxides, aralkylperoxides, peroxide ethers, peroxide esters, such as di-tert.-butylperoxide, bis-(tert.-butylperoxyisopropyl)-benzene, dicumylperoxide, 2,5-dimethyl-2,5- di(tert.-butylperoxy)-hexane, 2,5-dimethyl-2,5-di(tert.-butylperoxy)-hexene-(3), 1 ,1- bis-(tert.-butylperoxy)-3,3,5-trimethyl-cyclohexane, benzoylperoxide, tert.-butyl- cumylperoxide and tert.-butylperbenzoate.
  • organic peroxides such as dialkylperoxides, ketalperoxides,
  • the curable rubber compound according to the invention can contain further auxiliary products for rubbers, such as reaction accelerators, vulcanizing accelerators, vulcanizing acceleration auxiliaries, antioxidants, foaming agents, anti-aging agents, heat stabilizers, light stabilizers, ozone stabilizers, plasticizers, tackifiers, blowing agents, dyestuffs, pigments, waxes, extenders, organic acids, inhibitors, metal oxides, and activators such as triethanolamine, polyethylene glycol, hexanetriol, etc., which are known to the rubber industry.
  • the rubber aids are used in conventional amounts, which depend inter alia on the intended use. Conventional amounts are e.g. from 0.1 to 50 phr.
  • the ingredients of the rubber compound are often mixed together, suitably at an elevated temperature that may range from 25 °C to 200 °C. Normally the mixing time does not exceed one hour and a time in the range from 2 to 30 minutes is usually adequate.
  • the mixing of the rubbers, optionally the filler(s), optionally vulcanization agent, and/or further ingredients is suitably carried out in an internal mixer such as a Banbury mixer, or a Haake or Brabender internal mixer.
  • a two roll mill mixer also provides a good dispersion of the compounds within the final product.
  • An extruder also provides good mixing, and permits shorter mixing times.
  • the masterbatch and the curable rubber compound according to the present invention are very well suited for the manufacture of a shaped article, such as a seal, hose, bearing pad, stator, well head seal, valve plate, cable sheathing, wheel roller, pipe seal, in place gaskets or footwear component. Furthermore, they are very well suited for wire and cable production.
  • the masterbatch provides a compound possessing enhanced processability due to lower compound Mooney viscosity and quicker Mooney relaxation times compared to rubber compounds conventionally prepared. Also, rubber compounds containing rubber masterbatches according to the present invention have improved physical properties, in particular, higher moduli or overall compound stiffness.
  • Carbon black N774 and N990 are both available from Cabot Corp.
  • ElastomagTM 170 Powder is magnesium oxide available from Morton International.
  • NaugardTM 445 is p-dicumyl diphenylamine and is available through Crompton Corp..
  • PlasthallTM TOTM is a trioctyl trimellitate from The CP. Hall Co., Inc..
  • RhenogranTM PCD-50 is a polycarbodiimide from Rhein Chemie Corp..
  • Stearic Acid EmersolTM 132 NF is stearic acid available from Acme- Hardesty Co..
  • TP-759 is an ether/ester based plasticizer available from Morton International.
  • VulkanoxTM ZMB-2/C5 is the zinc salt of 4- and 5-methyl mercaptobenzimidazole (ZMMBI) and is available from Lanxess Deutschland GmbH.
  • Zinc Oxide (KadoxTM 920) is available from St. Lawrence Chem. Inc.
  • TAIC-DLC-A is triallyl isocyanurate (72% by weight) on a silicon dioxide carrier available from Natrochem, Inc..
  • VulcupTM 40KE is a bis 2-(t-butyl-peroxy) diisopropylbenzene (40% on Burgess clay) available from Geo Specialty Chemicals, Inc..
  • the compound Mooney viscosity was determined at 100 0 C using a large rotor.
  • the sample was preheated within the rotor cavity for one minute and then, subjected to the shearing action of the viscometer disk rotating at 2 rpm for a period of 4 minutes.
  • the torque in Mooney units was immediately recorded at that time.
  • the sample was then allowed to relax for a period of 4 minutes in order to acquire information about the relaxation behavior of the rubber compound.
  • the slope, intercept and area under the relaxation curve are all recorded.
  • the tests were compliant with ASTM D-1646.
  • the compound Mooney scorch was measured using a large rotor and a temperature of 135°C. The time at which the Mooney viscosity increases 5 Mooney units from the minimum value was recorded as tO5 in minutes. The test was run in compliance with ASTM D-1646. Rheometry
  • a Moving Die Rheometer (MDR 2000(E)) was used in order to follow the vulcanization behavior of the rubber samples. The platens were set at 180 0 C and a frequency of oscillation of 1.7 Hz coupled with a 1 ° arc were applied to the sample for a time of 30 minutes. This test procedure complies with ASTM D- 5289. Hardness
  • Tensile slabs were prepared by curing the rubber samples for 12 minutes at 180 0 C. Standard die C dumbbells were died out afterwards for testing. Testing was carried out at 23°C and the procedure complies with ASTM D-412 Method A. Tear Resistance Die B and die C geometries were cut out of a tensile sheet which was cured for 12 minutes at 180 0 C. The test complies with ASTM D-624. Compression Set
  • Solid compression buttons were prepared by curing the rubber samples 17 minutes at 180°C. Afterwards, the buttons were compressed 25% in a compression set jig and placed in a hot air oven set at 150 0 C for 70 and 168 hours. The test procedure complies with ASTM D-395 (Method B).
  • the present inventive masterbatches containing the ingredients listed in Table 1 were mixed according to the following procedure.
  • An internal Banbury type mixer with tangential rotors and a mixing capacity of 1.57 liters was employed.
  • the rotor speed was initially set at 77 rpm and the water was set for cooling at 30 0 C.
  • a batch factor of 73% was used.
  • all three polymers and the stearic acid were added into the mixing chamber and the ram was lowered.
  • the ram was raised after 2 minutes to perform a sweep and then lowered for the remainder of the mix.
  • the mix was dumped after 5 minutes of total mixing time. Temperatures did not surpass 125°C using this method. Scale up methods of such mixes may require the lowering of the rotor speed during the mix in order to prevent the temperature from exceeding 125°C.
  • the dumped masterbatch blend was then placed on a 10" by 20" two roll mill with the cooling water set at 3O 0 C.
  • the masterbatch was banded on the mill and refined by using 3/4 cuts. Six endwise passes was also performed to ensure maximum dispersive mixing of the polymers within the masterbatch.
  • the mixing of the rubber compound ingredients given in Table 2 was completed in two stages.
  • an internal BR-82 Banbury mixer with tangential rotors turning at 77 rpm was used.
  • the mixing chamber has a volume of 1.6 liters and the water was set for cooling at 30 0 C.
  • the fill factor was 0.73.
  • the inventive masterbatches or the Levapren® and Therban® polymers used for comparison were added to the mixing chamber and allowed to mix for 1 minute.
  • the carbon black, magnesium oxide, antioxidants (diphenylamine, ZMMBI and polycarbodiimide), TOTM and TP-759 plasticizers, stearic acid and zinc oxide were all added to the mixer. Mixing continued for another 2 minutes.
  • Table 3 illustrates that the compounds prepared with the rubber masterbatch (Ex, 1 , 3 and 5) still possess excellent scorch safety compared to the ones produced conventionally (Ex. 2, 4 and 6). Extra mixing of elastomers is sometimes a cause for a concern especially if degradation effects could arise.
  • Table 4 clearly shows the improvement in compound Mooney viscosity comparing Ex.1 to Ex.2, Ex. 3 to Ex. 4 and finally Ex. 5 to Ex. 6.
  • a lower compound Mooney viscosity translates to easier processing for compression, transfer or injection molding.
  • the quicker relaxation times illustrated by the lower time to decay, the more negative Mooney slopes, the lower intercept values and finally the smaller area under the relaxation curve are all indicative of a material possessing better processability characteristics.
  • Table 7 illustrates that the compression set values are only slightly influenced by using the rubber masterbatch technology.
  • Tables 8 and 9 illustrate that the rubber masterbatch produced compounds age in a similar manner as the conventional prepared ones in service fluid 105.
  • Table 10 illustrates that low temperature properties are not harmed in using the rubber masterbatch compounds versus the conventionally mixed compounds.

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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)
  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

La présente invention concerne un mélange maître de caoutchouc contenant au moins un polymère de nitrile hydrogéné, au moins deux polymères oléfine-acétate de vinyle et au moins un auxiliaire de traitement. La présente invention concerne également un composé de caoutchouc durcissable contenant ledit mélange maître, au moins un agent de vulcanisation et au moins une charge. La présente invention concerne en outre un article façonné contenant ledit composé de caoutchouc durcissable.
PCT/CA2005/001887 2004-12-20 2005-12-13 Melanges maitres de caoutchouc Ceased WO2006066394A1 (fr)

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US63750104P 2004-12-20 2004-12-20
US60/637,501 2004-12-20

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102329441A (zh) * 2011-07-22 2012-01-25 陆洪兴 塑胶交通护栏及其制备方法
EP2292687B1 (fr) * 2009-09-03 2012-07-25 Rhein Chemie Rheinau GmbH Mélanges vulcanisables améliorés exempts de guanidine contenant des caoutchoucs à base d'éthylène acrylate (AEM), polyacrylate (ACM), et/ou acrylnitrile hydrogéné (HNBR), vulcanisats préparés par réticulation de ces mélanges vulcanisables et leur utilisation
WO2015193920A3 (fr) * 2014-06-20 2016-03-31 Zenith Industrial Rubber Products Pvt. Ltd. Caoutchouc pré-réticulé et procédé pour sa fabrication
CN108276685A (zh) * 2017-12-29 2018-07-13 安徽天星电缆科技有限公司 一种高拉伸强度机器人手臂扭转电缆料
WO2020020630A3 (fr) * 2018-07-23 2020-03-19 Arlanxeo Deutschland Gmbh Hydrogénation de caoutchouc nitrile

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US4675248A (en) * 1983-10-29 1987-06-23 Bayer Aktiengesellschaft Polymer mixtures and co-vulcanizates produced therefrom
EP0272071A1 (fr) * 1986-12-16 1988-06-22 BICC Public Limited Company Compositions élastomères
JPH02160850A (ja) * 1988-12-14 1990-06-20 Fujikura Ltd 半導電性樹脂組成物および電力ケーブル
EP0531788A1 (fr) * 1991-09-06 1993-03-17 Bayer Ag Mélanges élastomères vulcanisables
CA2292158A1 (fr) * 1999-12-15 2001-06-15 Bayer Inc. Composition polymerique amelioree et methode de production de vulcanisats a partir de cette composition
CA2436742A1 (fr) * 2003-06-26 2004-12-26 Bayer Inc. Melanges de polymeres contenant du caoutchouc nitrile

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Publication number Priority date Publication date Assignee Title
US4675248A (en) * 1983-10-29 1987-06-23 Bayer Aktiengesellschaft Polymer mixtures and co-vulcanizates produced therefrom
EP0272071A1 (fr) * 1986-12-16 1988-06-22 BICC Public Limited Company Compositions élastomères
JPH02160850A (ja) * 1988-12-14 1990-06-20 Fujikura Ltd 半導電性樹脂組成物および電力ケーブル
EP0531788A1 (fr) * 1991-09-06 1993-03-17 Bayer Ag Mélanges élastomères vulcanisables
CA2292158A1 (fr) * 1999-12-15 2001-06-15 Bayer Inc. Composition polymerique amelioree et methode de production de vulcanisats a partir de cette composition
CA2436742A1 (fr) * 2003-06-26 2004-12-26 Bayer Inc. Melanges de polymeres contenant du caoutchouc nitrile

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2292687B1 (fr) * 2009-09-03 2012-07-25 Rhein Chemie Rheinau GmbH Mélanges vulcanisables améliorés exempts de guanidine contenant des caoutchoucs à base d'éthylène acrylate (AEM), polyacrylate (ACM), et/ou acrylnitrile hydrogéné (HNBR), vulcanisats préparés par réticulation de ces mélanges vulcanisables et leur utilisation
CN102329441A (zh) * 2011-07-22 2012-01-25 陆洪兴 塑胶交通护栏及其制备方法
CN102329441B (zh) * 2011-07-22 2016-01-06 江阴市人人达科技有限公司 塑胶交通护栏及其制备方法
WO2015193920A3 (fr) * 2014-06-20 2016-03-31 Zenith Industrial Rubber Products Pvt. Ltd. Caoutchouc pré-réticulé et procédé pour sa fabrication
CN108276685A (zh) * 2017-12-29 2018-07-13 安徽天星电缆科技有限公司 一种高拉伸强度机器人手臂扭转电缆料
WO2020020630A3 (fr) * 2018-07-23 2020-03-19 Arlanxeo Deutschland Gmbh Hydrogénation de caoutchouc nitrile
CN112449643A (zh) * 2018-07-23 2021-03-05 阿朗新科德国有限责任公司 丁腈橡胶的氢化
US11312791B2 (en) 2018-07-23 2022-04-26 Arlanxeo Deutschland Gmbh Hydrogenation of nitrile rubber
CN112449643B (zh) * 2018-07-23 2023-03-14 阿朗新科德国有限责任公司 丁腈橡胶的氢化

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