Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/04—Oxygen-containing compounds
  • C08K5/13—Phenols; Phenolates
• • 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
  • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
  • C08K5/005—Stabilisers against oxidation, heat, light, ozone
• • 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
  • C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
  • C08K5/37—Thiols
  • C08K5/372—Sulfides, e.g. R-(S)x-R'
• • 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
  • C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
  • C08K5/37—Thiols
  • C08K5/375—Thiols containing six-membered aromatic rings

Definitions

• the present invention relates to a composition for cross-linking and stabilization of polymers containing hydrolysable silane groups which comprises a sulphonic acid as a silanol condensation catalyst. Further, the present invention relates to a stabilized polymer containing cross-linked silane groups wherein the cross-linking has been performed by the use of a sulphonic acid as a silanol condensation catalyst and to a process for cross-linking and stabilization of silane group containing polymers by the use of a sulphonic acid as a silanol condensation catalyst.
• cross-link polymers by means of additives as this improves the properties of the polymer such as mechanical strength and chemical heat resistance.
• Cross-linking may be performed by condensation of silanol groups contained in the polymer which can be obtained by hydrolysation of silane groups.
• a silanol condensation catalyst For cross-linking of such polymers, a silanol condensation catalyst must be used.
• Conventional catalysts are for example tin-organic compounds such as dibutyl tin dilaurate (DBTDL).
• DBTDL dibutyl tin dilaurate
• the cross-linking process advantageously is carried out in the presence of acidic silanol condensation catalysts.
• acidic catalysts allow cross-linking to quickly take place already at room temperature.
• Such acidic silanol condensation catalysts are disclosed for example in WO 95/17463.
• stabilizers are added to the polymer which protect it from degradation caused by thermal oxidation, UV-radiation, processing and by penetration of metal.
• ions such as copper ions.
• the stabilizer must be added to the polymer before the cross-linking step is performed.
• the stabilizer usually is added to the polymer together with the silanol condensation catalyst, preferably in the form of a master batch.
• the stabilizer must be therefore compatible with the silanol condensation catalyst, i.e. must not degrade on contact with the catalyst as this may lead to exudation, i.e. migration of the stabilizer or fragments thereof to the surface of the composition or the polymer. Exudation may already occur in the masterbatch which causes problems during processing of the polymer e.g. in an extruder, where during the extrusion of the silane group containing polymer mixed with the cross-linking composition the catalyst feeder is blocked. Such a blocking may lead to a lowering of catalyst added to the polymer and hence to an uncontrolled deterioration of the properties of the finally produced polymer.
• the degradation of the stabilizer may also lead to volatile low molecule substances which evaporate into the air and thus cause a bad smell.
• the degradation of the stabilizer deteriorates the ageing properties of the polymer as a lower amount of original stabilizer is present in the polymer.
• the stabilizer must not inhibit or lower the activity of the catalyst, or negatively effect other properties of the polymer on contact with the catalyst.
• Most common stabilizers for cross-linked polymers include ester group containing compounds such as Irganox 1010, Irganox 1035 and Irganox 1076 of Ciba-Geigy.
• ester group containing compounds such as Irganox 1010, Irganox 1035 and Irganox 1076 of Ciba-Geigy.
• these common stabilizers degrade when mixed with acidic silanol condensation catalysts, e.g. in a master batch, thus leading to exudation. This is the case even if the master batch is kept water free by the addition of water absorbing additives, which inhibits the acid catalysed ester cleavage.
• Stabilizers containing basic groups or metal soaps inhibit the activity of a sulphonic acid silanol condensation catalyst.
• Stabilizers containing aromatic sulfur groups i.e. groups wherein a sulfur atom is directly linked to an aromatic group, also degrade in the presence of acidic silanol condensation catalysts leading to bad smell.
• the present invention is based on the finding that such a stabilizer must be neutral or acidic, must comprise a sterically hindered phenol group or aliphatic sulphur groups and must not contain ester groups.
• the present invention therefore provides a composition for cross-linking and stabilization of polymers containing hydrolysable silane groups comprising a sulphonic acid as a silonal condensation catalyst which comprises a stabilizer which is neutral or acidic, does not contain ester groups and is a compound according to formula (I):
• R is an unsubstituted or substituted aliphatic or aromatic hydrocarbyl radical which may comprise heteroatoms
• R′ is a hydrocarbyl radical
• R′′ is a hydrocarbyl radical
• R′ and/or R′′ being a bulky radical
• X 1 , X 2 and X 3 is the same or different H or OH, whereby at least X 1 , X 2 or X 3 is OH,
• n 1 to 4.
• R′′′ is an aliphatic hydrocarbyl radical
• p is 1 to 6.
• R is unsubstituted. However, if R is substituted it is preferred that it contains only hydroxy radicals as substituents.
• Heteroatoms may also be present in R, such as O-atoms forming ether groups, for example, if the stabilizer is produced in an oligomerisation reaction from phenolic compounds, or S-atoms which however may not be directly linked to an aromatic group.
• n in formula (I) is 2 or 3.
• R′ is a bulky hydrocarbyl radical.
• X 1 in formula (I) is OH.
• p in formula (II) is 1 or 2.
• the present invention provides a stabilized polymer which contains cross-linked silane groups wherein the cross-linking has been performed by use of a sulphonic acid as a silanol condensation catalyst which comprise a stabilizer as specified above for the inventive composition. Further, the invention provides a process for cross-linking and stabilization of silane group containing polymers by the use of a sulphonic acid as a silanol condensation catalyst wherein the process is carried out in the presence of a stabilizer as specified above for the inventive composition.
• inventive composition, polymer or process may as a stabilizer either comprise a single compound as characterized above or a mixture thereof.
• the stabilizer in the inventive composition does not degrade the desired amelioration of ageing properties of the polymer can be achieved.
• the inventive composition comprises a stabilizer which is neutral or acidic, does not contain ester groups and is a compound according to formula (I)
• R is an aliphatic hydrocarbyl radical which may comprise hydroxy groups
• X 1 is OH
• X 2 and X 3 is H
• R′ is a bulky aliphatic hydrocarbyl radical
• R′′ is an aliphatic hydrocarbyl radical
• n 2;
• R′′′ is an aliphatic hydrocarbyl radical from C 12 to C 20 and
• p is 1 or 2.
• R in formula (I) is CH 2 .
• the inventive composition comprises a stabilizer which is selected from the group of 2,2′-methylene-bis(6-(1-methyl-cyclohexyl)para-cresol) (corresponding to the compound of formula (I) wherein R is CH 2 , R′ is 1-methyl-cyclohexyl, R′′ is CH 3 , X 1 is OH, X 2 and X 3 is H and n is 2), 2,2′-methylene-bis(4-methyl-6-tert.-butylphenol) (corresponds to the compound of formula (I) wherein R is CH 2 , R′ is tert.-butyl, R′′ is CH 3 , X 1 is OH, X 2 and X 3 is H and n is 2), and di-octadecyl-disulphide (corresponding to the compound of formula (II) wherein R′′′ is octadecyl and p is 2).
• a stabilizer which is selected from the group of 2,2′-methylene
• This stabilizer is also further preferred in the inventive polymer and process.
• the inventive composition comprises 2-2′-methylene-bis(6-(1methyl-cyclohexyl)para-cresol) as a stabilizer. It is also particularly preferred that the inventive polymer as well as the inventive process comprise this stabilizer.
• This particular preferred stabilizer may also be advantageously used in a mixture with 2,2′-methylene-bis(4-methyl-6-tert.-butylphenol).
• the inventive composition is preferably added to the cross-linkable polymer in the form of a master batch, i.e. the additives such as the catalyst and the stabilizer are mixed with a polymer such as a homo- or copolymer of ethylene, e.g. low density polyethylene or polyethylene-methyl-ethyl-butyl-acrylate copolymer containing 1 to 50 percent by weight of the acrylate and mixtures thereof.
• a polymer such as a homo- or copolymer of ethylene, e.g. low density polyethylene or polyethylene-methyl-ethyl-butyl-acrylate copolymer containing 1 to 50 percent by weight of the acrylate and mixtures thereof.
• Further constituents of the master batch may be for example a drying agent and a scorch retardant.
• the master match contains a minor amount of the stabilizer, generally about 0.01 to 4 wt %, preferably about 0.02 to 2 wt %.
• the stabilizer in general is present in an amount of at most 2 wt %, preferably from 0.1 to 0.5 wt % and most preferred from 0.15 to 0.3 wt %.
• the silanol condensation catalyst is a sulphonic acid compound according to formula (III)
• Ar being a hydrocarbyl substituted aryl group and the total compound containing 14 to 28 carbon atoms.
• the Ar group is a hydrocarbyl substituted benzene or naphthalene ring, the hydrocarbyl radical or radicals containing 8 to 20 carbon atoms in the benzene case and 4 to 18 atoms in the naphthalene case.
• the hydrocarbyl radical is an alkyl substituent having 10 to 18 carbon atoms and still more preferred that the alkyl substituent contains 12 carbon atoms and is selected from dodecyl and tetrapropyl. Due to commercial availability it is most preferred that the aryl group is a benzene substituted group with an alkyl substituent containing 12 carbon atoms.
• the currently most preferred compounds of formula (III) are dodecyl benzene sulphonic acid and tetrapropyl benzene sulphonic acid.
• the silanol condensation catalyst may also be precursor of a compound of formula (III), i.e. a compound that is converted by hydrolysis to a compound of formula (III).
• a precursor is for example the acid anhydride of the sulphonic acid compound of formula (III).
• a sulphonic acid of formula (III) that has been provided with a hydrolysable protective group as e.g. an acetyl group which can be removed by hydrolysis to give the sulphonic acid of formula (III).
• the preferred amount of silanol condensation catalyst with respect to the cross-linkable polymer composition is from 0.0001 to 3 wt %, more preferably 0.001 to 2 weight % and most preferably 0.005 to 1 weight % based on the amount of silanol groups containing polymers in the composition.
• the effective amount of catalyst depends on the molecular weight of the catalyst used. Thus, a smaller amount is required of a catalyst having a low molecular weight than a catalyst having a high molecular weight.
• the catalyst is contained in a master batch it is preferred that it comprises the catalyst in an amount of 0.02 to 5 wt %, more preferably about 0.05 to 2 wt %.
• the present invention generally concerns cross-linkable polymers containing hydrolysable silane groups. More preferably the cross-linkable polymer is a polyolefin and still more preferably is a polyethylene.
• the hydrolysable silane groups may be introduced into the polymer by copolymerization of e.g. ethylene monomers with silane group containing comonomers or by grafting, i.e. by chemical modification of the polymer by addition of silane groups mostly in a radical reaction. Both techniques are well known in the art.
• the silane group containing polymer has been obtained by copolymerization.
• the copolymerization is preferably carried out with an unsaturated silane compound represented by the formula
• R 1 is an ethylenically unsaturated hydrocarbyl, hydrocarbyloxy or (meth)acryloxy hydrocarbyl group
• R 2 is an aliphatic saturated hydrocarbyl group
• Y which may be the same or different, is a hydrolysable organic group and
• q is 0, 1 or 2.
• the unsaturated silane compound are those wherein R 1 is vinyl, allyl, isopropenyl, butenyl, cyclohexanyl or gamma(meth)-acryloxy propyl; Y is methoxy, ethoxy, formyloxy, acetoxy, propionyloxy or an alkyl-or arylamino group; and R 2 , if present, is a methyl, ethyl, propyl, decyl or phenyl group.
• a preferred unsaturated silane compound is represented by the formula
• A is a hydrocarbyl group having 1-8 carbon atoms, preferably 1-4 carbon atoms.
• the most preferred compounds are vinyl trimethoxysilane, vinyl bismethoxyethoxysilane, vinyl triethoxysilane, gamma-(meth)acryloxypropyltrimethoxysilane, gamma(meth)acryloxypropyltriethoxy-silane, and vinyl triacetoxysilane.
• the copolymerization of the olefin, e.g. ethylene, and the unsaturated silane compound may be carried out under any suitable conditions resulting in the copolymerization of the two monomers.
• the copolymerization may be implemented in the presence of one or more other comonomers which can be copolymerized with the two monomers.
• comonomers include (a) vinyl carboxylate esters, such as vinyl acetate and vinyl pivalate, (b) alpha-olefins, such as propene, 1-butene, 1-hexane, 1-octene and 4-methyl-1-pentene, (c) (meth)acrylates, such as methyl(meth)acrylate, ethyl(meth)acrylate and butyl(meth)acrylate, (d) olefinically unsaturated carboxylic acids, such as (meth)acrylic acid, maleic acid and fumaric acid, (e) (meth)acrylic acid derivativs, such as (meth)acrylonitrile and (meth)acrylic amide, (f) vinyl ethers, such as vinyl methyl ether and vinyl phenyl ether, and (
• vinyl esters of monocarboxylic acids having 1-4 carbon atoms such as vinyl acetate
• (meth)acrylate of alcohols having 1-4 carbon atoms such as methyl(meth)-acrylate
• Especially preferred comonomers are butyl acrylate, ethyl acrylate and methyl acrylate.
• the term “(meth)acrylic acid” is intended to embrace both acrylic acid and methacrylic acid.
• the comonomer content of the copolymer may amount to 70% by weight of the copolymer, preferably about 0.5 to 35% by weight, most preferably about 1 to 30% by weight.
• the silane-containing polymer according to the invention suitably contains 0.001-15% by weight of the silane compound, preferably 0.01-5% by weight, most preferably 0.1-2% by weight.
• inventive polymer composition may further contain varies additives, such as miscible thermoplastics, further stabilizers, lubricants, fillers, coloring agents and foaming agents.
• additives such as miscible thermoplastics, further stabilizers, lubricants, fillers, coloring agents and foaming agents.
• the compounds 4,4′-thiobis(2-tert.butyl-5-methylphenol) (Lowinox TBM6P), 2,2′-thiodiethylenebis-(3,5-di-tert.butyl-4-hydroxyphenyl)-propionate (Irganox 1035), octadecyl-3-(3′,5′-di-tert.-butyl-4-hydroxyphenyl)propionate (Irganox 1076), di-lauryl-thio-di-propionate (Irganox PS 802) and tris(2-tert.-butyl-4-thio(2′-methyl-4′hydroxy-5′-tert.-butyl)phenyl-5-methyl)phenylphosphite (Hostanox OSP1) as comparative examples, and 1,3,5-tri-methyl-2,4,6-tris-(3,5-di-tert.butyl-4-hydroxyphenyl)benz
• Pellet samples were prepared according to 1. and were stored for seven days at 23° C. or twenty-one days at 55° C. and seven days at 23° C. in heat sealed hermetic closed Al-foiled polyethylene bags. Before and after this treatment, 20 gram of pellets sample and 50-ml isopropyl alcohol were added to a glass beaker. The mixtures were blended with a magnetic mixer for five minutes. Thereby, the isopropyl alcohol extracted the stabiliser from the pellet surface. 2 ml of the liquid phase was filtered into a Vials.

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