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WO1997030112A1 - Stabilisation de produits de recyclage de polyolefines - Google Patents

Stabilisation de produits de recyclage de polyolefines Download PDF

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Publication number
WO1997030112A1
WO1997030112A1 PCT/EP1997/000497 EP9700497W WO9730112A1 WO 1997030112 A1 WO1997030112 A1 WO 1997030112A1 EP 9700497 W EP9700497 W EP 9700497W WO 9730112 A1 WO9730112 A1 WO 9730112A1
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WO
WIPO (PCT)
Prior art keywords
hydrogen
alkyl
tert
butyl
bis
Prior art date
Application number
PCT/EP1997/000497
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English (en)
Inventor
Rudolf Pfaendner
Heinz Herbst
Kurt Hoffmann
Original Assignee
Ciba Specialty Chemicals Holding Inc.
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 Ciba Specialty Chemicals Holding Inc. filed Critical Ciba Specialty Chemicals Holding Inc.
Priority to AU16005/97A priority Critical patent/AU1600597A/en
Priority to JP9528943A priority patent/JP2000506185A/ja
Priority to EP97902320A priority patent/EP0880557A1/fr
Publication of WO1997030112A1 publication Critical patent/WO1997030112A1/fr

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    • 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
    • C08K5/15—Heterocyclic compounds having oxygen in the ring
    • C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
    • C08K5/1515—Three-membered rings
    • 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
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/17—Amines; Quaternary ammonium compounds
    • C08K5/18—Amines; Quaternary ammonium compounds with aromatically bound amino groups

Definitions

  • the invention relates to a process for stabilizing polyolefin recyclates, to a stabilizer mixture, and to the recycled polyolefins obtainable by the process.
  • the object of the present invention was therefore to provide a stabilization system which has very good stabilizing properties and consists as far as possible of liquid, homogeneously miscible components. Furthermore, the stabilizer system should be economically acceptable for use in recyclates, i.e. it should either be effective in low concentrations or consist of inexpensive components.
  • a mixture comprising a secondary aromatic amine and a polyfunctional epoxide is particularly suitable for stabilizing polyolefin recyclates in accordance with the requirements set out above.
  • the present invention therefore provides a process for stabilizing a polyolefin recyclate against oxidative, thermal or light-induced degradation, which comprises adding thereto at least one secondary aromatic amine and at least one polyfunctional epoxide.
  • the invention is particularly important in connection with polyolefin recyclates as are obtained from production waste, collections of recyclable material from households, in retail outlets or through obligatory takeback schemes, for example in the automotive industry, such as for old battery cases, or in the electrical sector.
  • films such as agricultural films, pouches, bottles and other containers.
  • these recyclates may also, in minor amounts, include admixed plastics of different structure, for example styrene polymers (IPS, EPS, ABS, ASA), polyesters (PET) or polyamides, and also customary impurities, for example paint residues, traces of metal, fuel residues, ethylene glycol, isopropanol or else traces of water.
  • plastics of different structure for example styrene polymers (IPS, EPS, ABS, ASA), polyesters (PET) or polyamides, and also customary impurities, for example paint residues, traces of metal, fuel residues, ethylene glycol, isopropanol or else traces of water.
  • Polyolefin recyclates are derived from the following pure polyolefins:
  • Polymers of mono- and diolefins for example polypropylene, polyisobutylene, polybut-1- ene, poly-4-methylpent-1 -ene, polyisoprene or polybutadiene, and also polymers of cycloolefins, for example of cyclopentene or norbornene; furthermore polyethylene (which can be crosslinked), for example high-density polyethylene (HDPE), high-density polyethylene of high molar mass (HDPE-HMW), high-density polyethylene of ultra high molar mass (HDPE-UHMW), medium-density polyethylene (MDPE), low-density polyethylene (LDPE), linear low-density polyethylene (LLDPE) and branched low-density polyethylene (VLDPE).
  • HDPE high-density polyethylene
  • HDPE-HMW high-density polyethylene of high molar mass
  • HDPE-UHMW high-density polyethylene of ultra high
  • Polyolefins i.e. polymers of monoolefins exemplified in the preceding paragraph, especially polyethylene and polypropylene, can be prepared by different, and especially by the following, methods:
  • the catalyst normally containing one or more metals of group IVb, Vb, VIb or Vlll.
  • metals usually have one or more ligands, such as oxides, halides, alcoholates, esters, ethers, amines, alkyls, alkenyls and/or aryls that may be either ⁇ - or ⁇ -coordinated.
  • ligands such as oxides, halides, alcoholates, esters, ethers, amines, alkyls, alkenyls and/or aryls that may be either ⁇ - or ⁇ -coordinated.
  • These metal complexes may be in free form or fixed on substrates, for example on activated magnesium chloride, titanium (III) chloride alumina or silica.
  • These catalysts may be soluble or insoluble in the polymerization medium.
  • the catalysts can be active as such in the polymerization or further activators may be used, for example metal alkyls, metal hydrides, metal alkyl halides, metal alkyl oxides or metal alkyloxanes.
  • the metals being elements of groups la, lla and/or Ilia.
  • the activators may be modified, for example, with further ester, ether, amine or silyl ether groups.
  • These catalysts are usually termed Phillips, Standard Oil Indiana, Ziegler (-Natta), TNZ (DuPont), metallocene or single site catalysts (SSC).
  • Mixtures of the polymers mentioned under 1 for example mixtures of polypropylene with polyisobutylene, polypropylene and polyethylene (e.g. PP/HDPE, PP/LDPE) and mixtures of different types of polyethylene (e.g. LDPE/HDPE).
  • Copolymers of monoolefins and diolefins with each other or with other vinyl monomers for example ethylene-propylene copolymers, linear low-density polyethylene (LDPE) and mixtures thereof with low-density polyethylene (LDPE), propylene-but-1 -ene copolymers, propylene-isobutylene copolymers, ethylene-but-1 -ene copolymers, ethylene-hexene copolymers, ethylene-methylpentene copolymers, ethylene-heptene copolymers, ethylene- octene copolymers, propylene-butadiene copolymers, isobutylene-isoprene copolymers, ethylene-alkyl acrylate copolymers, ethylene-alkyl methacrylate copolymers, ethylene-vinyl acetate copolymers and copolymers thereof with carbon monoxide, or ethylene-acrylic acid copolymers
  • the polyolefin recyclate is preferably a copolymer recyclate of mono- and diolefins, especially a polypropylene copolymer recyclate from battery cases or a polyethylene copolymer recyclate.
  • Polyethylene recyclates or polypropylene recyclates are also particularly preferred.
  • Secondary aromatic amines are, for the purposes of this invention, preferably compounds of the formula I
  • Ri is hydrogen or C ⁇ -C 25 alkyl
  • R 2 is hydrogen, C ⁇ -C 2 alkyl or benzyl
  • R 3 is hydrogen, CrC 25 alkyl, C 3 -C ⁇ 2 cycloalkyl, benzyl, ⁇ -methylbenzyl or ⁇ ,cc-dimethylbenzyl;
  • R 4 is hydrogen, C ⁇ -C 2S alkyl or benzyl
  • R 5 is hydrogen or C ⁇ -C 25 alkyl
  • R ⁇ is hydrogen, d-C 25 alkyl or benzyl
  • R 7 is hydrogen, d-C ⁇ alkyl, C 5 -C ⁇ 2 cycloalkyl, benzyl, ⁇ -methylbenzyl, ⁇ , ⁇ -dimethylbenzyl or — N
  • R 8 is hydrogen, C ⁇ -C 25 alkyl or benzyl
  • R 9 is hydrogen or C ⁇ -C 25 alkyl
  • R 10 is C 5 -C 12 cycloalkyl
  • Alkyl of up to 25 carbon atoms is a branched or unbranched radical such as, for example, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 2-ethylbutyl, n-pentyl, isopentyl, 1-methylpentyl, 1 ,3-dimethylbutyl, n-hexyl, 1-methylhexyl, n-heptyl, isoheptyl, 1,1 ,3,3-tetramethylbutyl, 1-methylheptyl, 3-methylheptyl, n-octyl, 2-ethylhexyl, 1 ,1,3-trime- thylhexyl, 1 ,1 ,3,3-tetramethylpentyl, nonyl, decyl, undecyl, 1-methylundecyl, dode
  • Ri, R 2 , R 4 , R 5 , R ⁇ and R 8 is for example C C 18 alkyl, especially CrC ⁇ 2 alkyl, for instance C ⁇ -C ⁇ alkyl.
  • a preferred definition of R 3 and R 7 is for example C ⁇ -C ⁇ 8 alkyl, especially CrC ⁇ 2 alkyl, for instance C -C 12 alkyl.
  • a parti ⁇ cularly preferred definition of R 3 and R 7 is C 4 -C ⁇ oalkyl, especially C 4 -C ⁇ alkyl, for instance tert-butyl or tert-octyl.
  • C 5 -C ⁇ 2 cycloalkyl is, for example, cyclopentyl, cyclohexyl, cycloheptyi, cyclooctyl, cyclodecyl or cyclododecyl.
  • a preferred definition of R 3 , R 7 and Rio is for example Cs-C ⁇ cycloalkyl, es ⁇ pecially C 5 -C 7 cycloalkyl, for instance cyclohexyl.
  • Ri and R 2 independently of one another are hydrogen or CrC ⁇ ⁇ alkyl
  • R 3 is hydrogen, C ⁇ -C ⁇ ⁇ alkyl, Cs-C 8 cycloalkyl, benzyl, ⁇ -methylbenzyl or ⁇ , ⁇ -dimethylbenzyl;
  • R 4l R 5 and R 6 independently of one another are hydrogen or C ⁇ -C 8 alkyl
  • R is hydrogen, Ci-Ci ⁇ alkyl, C 5 -C ⁇ cycloalkyl, benzyl, ⁇ -methylbenzyl, ⁇ , ⁇ -dimethylbenzyl or — N
  • R 8 and R 9 independently of one another are hydrogen or C -C ⁇ 8 alkyl
  • R 10 is C 5 -C 8 cycloalkyl, T
  • R and R 2 are hydrogen
  • R 3 is hydrogen, C 4 -C ⁇ 2 alkyl, cyclohexyl, benzyl, ⁇ -methylbenzyl or ⁇ , ⁇ -dimethylbenzyl; or R 2
  • R , R 5 and R 6 are hydrogen
  • R 7 is hydrogen, cyclohexyl, benzyl, ⁇ -methylbenzyl, ⁇ , ⁇ -dimethylbenzyl or
  • R 8 and R 9 are hydrogen
  • Rio is cyclohexyl, phenyl or ⁇ -naphthyl.
  • R 7 is C 8 alkyl or — N and
  • R 10 is phenyl
  • polyfunctional epoxides can have an aliphatic, aromatic, cycloaliphatic, araliphatic or heterocyclic structure; they include epoxide groups as side groups, or these groups form part of an alicyclic or heterocyclic ring system.
  • the epoxide groups are preferably attached as glycidyl groups to the remainder of the molecule by way of ether or ester linkages, or the compounds involved are N-glycidyl derivatives of hetero ⁇ cyclic amines, amides or imides. Epoxides of these types are generally known and commer ⁇ cially available.
  • polyfunctional epoxides comprise two epoxide radicals, for example those of the formu ⁇ la II
  • R and R ⁇ 3 which are attached directly to carbon, oxygen, nitrogen or sulfur atoms, in which R and R ⁇ 3 are both hydrogen, R ⁇ 2 is hydrogen or methyl and n is 0; or in which Ru and R ⁇ 3 together are -CH 2 CH 2 - or -CH 2 CH 2 CH 2 -, R ⁇ 2 is then hydrogen, and n is 0 or 1.
  • epoxides are: 1. Diglycidyl and di( ⁇ -methylglycidyl) esters obtainable by reacting a compound with two carboxyl groups in the molecule and epichlorohydrin and or glycerol dichlorohydrin and/or ⁇ -methylepichlorohydrin. The reaction is expediently carried out in the presence of bases.
  • aliphatic dicarboxylic acids can be used as compounds of two carboxyl groups in the molecule.
  • these dicarboxylic acids are glutaric acid, adipic acid, pimelic acid, sube ⁇ ric acid, azelaic acid, sebacic acid or dimerized or trimerized linoleic acid.
  • cycloaliphatic dicarboxylic acids for example tetrahy- drophthalic acid, 4-methyltetrahydrophthalic acid, hexahydrophthalic acid or 4-methylhexa- hydrophthalic acid.
  • aromatic dicarboxylic acids for example phthalic acid or isophthalic acid, can be used.
  • Diglycidyl, or di( ⁇ -methyiglycidyl) ethers obtainable by reacting a compound with two free alcoholic hydroxyl groups and/or phenolic hydroxyl groups and a suitable substituted epi ⁇ chlorohydrin under alkaline conditions, or in the presence of an acidic catalyst with subse ⁇ quent alkali treatment.
  • Ethers of this type are derived, for example, from acyclic alcohols, such as ethylene glycol, diethylene glycol and higher poly(oxyethylene) glycols, propane-1 ,2-diol,or polyoxypropy ⁇ lene) glycols, propane- 1 ,3-diol, butane-1 ,4-diol, poiy(oxytetramethylene) glycols, pentane- 1 ,5-diol, hexane-1 ,6-diol, sorbitol, and from polyepichlorohydrins.
  • acyclic alcohols such as ethylene glycol, diethylene glycol and higher poly(oxyethylene) glycols, propane-1 ,2-diol,or polyoxypropy ⁇ lene) glycols, propane- 1 ,3-diol, butane-1 ,4-diol, poiy(oxytetramethylene) glycols, pentane- 1
  • cycloaliphatic alcohols such as 1,3- or 1 ,4-dihydroxycyclohexane, bis(4-hydroxycyclohexyl)methane, 2,2-bis(4-hydroxycyclo-hexyl)- propane or 1 ,1-bis(hydroxymethyl)cyclohex-3-ene, or they possess aromatic nuclei, such as N,N-bis(2-hydroxyethyl)aniline or p,p'-bis(2-hydroxyethylamino)diphenylmethane.
  • aromatic nuclei such as N,N-bis(2-hydroxyethyl)aniline or p,p'-bis(2-hydroxyethylamino)diphenylmethane.
  • the epoxides can also be derived from mononuclear phenols, for example from resorcinol, pyrocatechol or hydroquinone; or they are based on poiynuclear phenols such as, for example, on 4,4'-dihydroxybiphenyl, bis(4-hydroxphenyl)methane, 2,2-bis(4-hydroxy-phe- nyl)propane, 2,2-bis(4-hydroxyphenyl)hexafluoropropane, 2,2-bis(3,5-dibromo-4-hydroxy- phenyl)propane, 4,4'-dihydroxybiphenyl sulfone, 9,9'-bis(4-hydroxyphenyl)fluorene, or on a condensate of phenols with formaldehyde obtained under acidic conditions, such as phenol novolaks.
  • mononuclear phenols for example from resorcinol, pyrocatechol
  • Di(N-glycidyl) compounds are obtainable, for example, by dehydrochlorination of the reaction products of epichlorohydrin with amines containing two amino hydrogen atoms.
  • amines containing two amino hydrogen atoms examples of these amines are aniline, toluidine, n-butylamine, bis(4-aminophenyl)methane, m-xylylenediamine or bis(4-methylaminophenyl)methane.
  • N,N'-diglycidyl derivatives of cycloalkyleneureas such as ethyleneurea or 1 ,3-propyleneurea
  • N,N'-diglycidyl deri ⁇ vatives of hydantoins such as of 5,5-dimethylhydantoin.
  • Di(S-glycidyl) compounds such as di-S-glycidyl derivatives derived from dithiols, for example ethane-1 ,2-dithiol or bis(4-mercaptomethylphenyl) ether.
  • Epoxides with a radical of the formula II in which Rn and R ⁇ 3 together are -CH 2 CH 2 - and n is 0 are, for example, bis(2,3-epoxycyclopentyl) ether, 2,3-epoxycyclopentyl glycidyl ether or 1 ,2-bis(2,3-epoxycyclopentyloxy)ethane;
  • examples of epoxides with a radical of the formula II in which R and R i3 together are -CH 2 CH 2 - and n is 1 are (3',4'-epoxy-6'-methylcyclohe- xyl)methyl 3,4-epoxy-6-methylcyclohexanecarboxylate and 3,4-epoxycyclohexylmethyl 3,4- epoxycyclohexanecarboxylate.
  • the abovementioned difunctional epoxides may include small amounts of mono- or trifunctional fractions.
  • polyfunctional epoxide is a di ⁇ functional epoxide.
  • suitable difunctional epoxides are:
  • liquid bisphenol A diglycidyl ethers such as Araldit®GY 240, Araldit®GY 250, Araldit®GY 260, Araldit®GY 266, Araldit®GY 2600 or Araldit®MY 790;
  • solid bisphenol A diglycidyl ethers such as Araldit®GT 6071 , Araldit®GT 7071 , Araldit®GT 7072, Araldit®GT 6063, Araldit®GT 7203, Araldit®GT 6064, Araldit®GT 7304, Araldit®GT 7004, Araldit®GT 6084, Araldit®GT 1999, Araldit®GT 7077, Araldit®GT 6097, Araldit®GT 7097, Araldit®GT 7008, Araldit®GT 6099, Araldit®GT 6608, Araldit®GT 6609 or Araldit®GT 6610;
  • Araldit®GT 6071 Araldit®GT 7071 , Araldit®GT 7072, Araldit®GT 6063, Araldit®GT 7203, Araldit®GT 6064, Araldit®GT 7304, Araldit®GT 7004, Araldit®
  • liquid bisphenol F diglycidyl ethers such as Araldit®GY 281 , Araldit®GY 282, Araldit®PY 302, or Araldit®PY 306;
  • liquid glycidyl ethers of alcohols such as Shell®Glycidyiether 162, Araldit®DY 0390 or Araldit®DY 0391;
  • liquid glycidyl esters of carboxylic acids such as Shell®Cardura E terephthalic ester, trimellitic ester, Araldit ⁇ PY 284 or mixtures of aromatic glycidyl esters, for example Araldit®PT 910;
  • liquid cycloaliphatic epoxy resins such as Araldit®CY 179.
  • tri- and polyfunctional epoxides can be employed supplementarily, in order, if desired, to obtain branching sites.
  • examples thereof which are suitable are:
  • solid and liquid polyglycidyl ethers of phenol-formaldehyde novolak such as EPN 1138, EPN 1139, GY 1180, PY 307
  • solid and liquid polyglycidyl ethers of o-cresole-formaldehyde novolak such as ECN 1235, ECN 1273, ECN 1280, ECN 1299;
  • difunctional epoxides are liquid or low-melting diglycidyl ethers based on bisphenols, for example on 2,2-bis-(4-hydroxyphenyl)propane (bisphenol A) or mixtures of bis(ortho/para-hydroxyphenyl)methane (bisphenol F).
  • Very particularly preferred epoxides are bisphenol A diglycidyl ethers, for example: Araldit®GT 6071 or Araldit®GY 260; bisphenol F diglycidyl ethers, for example Araldit® PY 306; liquid cycloaliphatic epoxy resins, for example Araldit®CY 179; or phenol novolak epoxy resins, e.g. Araldit®PY EPN 1139.
  • the process can be carried out in any vessels which can be heated and are fitted with a stirring device. These may, for example, be closed apparatus from which atmospheric oxy ⁇ gen is excluded, working for example under an inert gas atmosphere such as nitrogen.
  • the process is preferably conducted in an extruder.
  • the polyolefin recyclate to be heated and the mixture comprising a secondary aromatic amine and a difunctional epoxide are normally charged to the apparatus at the beginning of heating; however, subsequent metered addition of the novel mixture to the polyolefin re ⁇ cyclate is a further option, it being possible to add the mixture as such or else to add the individual components in any desired sequence.
  • the secondary aromatic amine and the polyfunctional epoxide can, indepen ⁇ dently of one another, be present in the form of a liquid, powder, granules or in compacted form, or else on a carrier material such as silica gel, or together with a polymer powder or wax, for example a polyethylene wax.
  • a carrier material such as silica gel
  • a polymer powder or wax for example a polyethylene wax.
  • liquid addition is pre ⁇ ferred.
  • polyolefin recyclate For each 100 parts of polyolefin recyclate, it is preferred to employ from 0.01 to 5 parts of a secondary aromatic amine and from 0.01 to 10 parts of a polyfunctional epoxide.
  • a secondary aromatic amine For each 100 parts of polyolefin recyclate, it is preferred to employ from 0.01 to 5 parts of a secondary aromatic amine and from 0.01 to 10 parts of a polyfunctional epoxide.
  • particular preference is given to the use of from 0.05 to 5 parts, especially from 0.05 to 2 parts, of a secondary aromatic amine, and from 0.05 to 5 parts, especially from 0.05 to 2 parts, of a polyfunctional epoxide.
  • the novel process has the advantage that the polyolefin recyclate is stabilized in short reac ⁇ tion times, and the additives, for example the secondary aromatic amine and the polyfunc ⁇ tional epoxide, can be added in liquid form.
  • the additives for example the secondary aromatic amine and the polyfunc ⁇ tional epoxide, can be added in liquid form.
  • the combination of secondary aromatic amines with polyfunctional epoxides leads synergistically to the stabilization of polyolefin recyclates.
  • the present invention also provides a mixture comprising a) a secondary aromatic amine and b) a polyfunctional epoxide, the weight ratio of the components a): b) being from 10:1 to 1:10, in particular from 5:1 to 1:5, for example from 2:1 to 1:2. Special preference is given to a weight ratio of components a): b) of from 1.5:1 to 1 :1.5, in particular from 1.1:1 to 1:1.1 , for example 1 :1.
  • additives can be added to the polyolefin recyclate.
  • additives include a secondary aromatic amine and a polyfunctional epoxide.
  • Alk lated monophenols for example 2,6-di-t ⁇ rt-butyl-4-methylphenol, 2-tert-butyl-4,6-di- methylphenol, 2,6-di-tert-butyl-4-ethylphenol, 2,6-di-tert-butyl-4-n-butylphenol, 2,6-di-tert-bu- tyl-4-isobutylphenol, 2,6-dicyclopentyl-4-methylphenol, 2-( ⁇ -methylcyclohexyl)-4,6-dimethyl- phenol, 2,6-dioctadecyl-4-methylphenol, 2,4,6-tricyclohexylphenol, 2,6-di-tert-butyl-4- methoxymethylphenol, nonylphenols which are linear or branched in the side chains, for example, 2,6-di-nonyl-4-methylphenoI, 2,4-dimethyl-6-(1 '-methylphenoI
  • Alkylthiomethylphenols for example 2,4-dioctylthiomethyl-6-tert-butylphenol, 2,4-dioc- tylthiomethyl-6-methylphenol, 2,4-dioctylthiomethyl-6-ethylphenol, 2,6-di-dodecylthiomethyl- 4-nonylphenol.
  • Hvdroquinones and alkylated hvdro ⁇ uinones for example 2,6-di-tert-butyl-4-methoxy- phenol, 2,5-di-tert-butylhydroquinone, 2,5-di-tert-amylhydroquinone, 2,6-diphenyl-4-octade- cyloxyphenol, 2,6-di-tert-butylhydroquinone, 2,5-di-tert-butyl-4-hydroxyanisole, 3,5-di-tert- butyl-4-hydroxyanisole, 3,5-di-tert-butyl-4-hydroxyphenyl stearate, bis-(3,5-di-tert-butyl-4- hydroxyphenyl) adipate.
  • Tocopherols for example ⁇ -tocopherol, ⁇ -tocopherol, ⁇ -tocopherol, ⁇ -tocopherol and mixtures thereof (Vitamin E).
  • Hvdroxylated thiodiphenyl ethers for example 2,2'-thiobis(6-tert-butyl-4-methylphenol), 2,2'-thiobis(4-octylphenol), 4,4'-thiobis(6-tert-butyl-3-methylphenol), 4,4'-thiobis(6-tert-butyl- 2-methylphenol), 4,4'-thiobis-(3,6-di-sec-amylphenol), 4,4'-bis(2,6-dimethyl-4-hydroxyphe- nyl)disulfide.
  • 2,2'-thiobis(6-tert-butyl-4-methylphenol 2,2'-thiobis(4-octylphenol), 4,4'-thiobis(6-tert-butyl-3-methylphenol), 4,4'-thiobis(6-tert-butyl- 2-methylphenol), 4,4'-thiobis-(3,6-di-sec-amylphenol), 4,
  • Alkylidenebisphenols for example 2,2'-methylenebis(6-tert-butyl-4-methylphenol), 2,2'- methylenebis(6-tert-butyl-4-ethylphenol), 2,2'-methylenebis[4-methyl-6-( ⁇ -methylcyclohexyl)- phenol], 2,2'-methylenebis(4-methyl-6-cyclohexylphenol), 2,2'-methylenebis(6-nonyl-4-me- thylphenol), 2,2 , -methylenebis(4,6-di-tert-butylphenol), 2,2'-ethylidenebis(4,6-di-tert-butyl- phenol), 2,2'-ethylidenebis(6-tert-butyl-4-isobutylphenol), 2,2'-methylenebis[6-(a-methylben- zyl)-4-nonylphenol], 2,2'-methylenebis[6-(a-methylb
  • N- and S-benzyl compounds for example 3,5,3 ⁇ 5 etra-tert-butyl-4,4'-dihydroxydi- benzyl ether, octadecyl-4-hydroxy-3,5-dimethylbenzylmercaptoacetate, tridecyl-4-hydroxy- 3,5-di-tert-butylbenzylmercaptoacetate, tris(3,5-di-tert-butyl-4-hydroxybenzyl)amine, bis(4- tert-butyl-3-hydroxy-2,6-dimethylbenzyl)dithioterephthalate, bis(3,5-di-tert-butyl-4-hydroxy- benzyl)sulfide, isooctyl-3,5-di-tert-butyl-4-hydroxybenzylmercaptoacetate.
  • hydroxybenzylated malonates for example dioctadecyl-2,2-bis-(3,5-di-tert-butyl-2-hy- droxybenzyl)-malonate, di-octadecyl-2-(3-tert-butyl-4-hydroxy-5-methylbenzyl)-malonate, di- dodecylmercaptoethyl-2,2-bis-(3,5-di-tert-butyl-4-hydroxybenzyl)malonate, bis[4-(1 ,1 ,3,3-te- tramethylbutyl)phenyl]-2,2-bis(3,5-di-tert-butyl-4-hydroxybenzyl)malonate.
  • dioctadecyl-2,2-bis-(3,5-di-tert-butyl-2-hy- droxybenzyl)-malonate di-octadecyl-2-(3-tert
  • Aromatic hvdroxybenzyl com p ounds, for example 1 ,3,5-tris-(3,5-di-tert-butyl-4-hydroxy- benzyl)-2,4,6-trimethylbenzene, 1 ,4-bis(3,5-di-tert-butyl-4-hydroxybenzyl)-2,3,5,6-tetrame- thylbenzene, 2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)phenol.
  • Triazine Compounds, for example 2,4-bis(octylmercapto)-6-(3,5-di-tert-butyl-4-hy- droxyanilino)-1 ,3,5-triazine, 2-octylmercapto-4,6-bis(3,5-di-tert-butyl-4-hydroxyanilino)-1 ,3,5- triazine, 2-octylmercapto-4,6-bis(3,5-di-tert-butyl-4-hydroxyphenoxy)-1 ,3,5-triazine, 2,4,6- tris(3,5-di-tert-butyl-4-hydroxyphenoxy)-1 ,2,3-triazine, 1 ,3,5-tris-(3,5-di-tert-butyl-4-hydroxy- benzyl)isocyanurate, 1,3,5-tris(4-tert-butyl-3-hydroxy-2,6-dimethylbenz
  • Benzylphosphonates for example dimethyl-2,5-di-tert-butyl-4-hydroxybenzylphospho- nate, diethyl-3,5-di-tert-butyl-4-hydroxybenzylphosphonate, dioctadecyl3,5-di-tert-butyl-4-hy- droxybenzylphosphonate, dioctadecyl-5-tert-butyl-4-hydroxy-3-methylbenzylphosphonate, the calcium salt of the monoethyl ester of 3,5-di-tert-butyl-4-hydroxybenzylphosphonic acid.
  • Acylaminophenols for example 4-hydroxylauranilide, 4-hydroxysteara ⁇ ilide, octyl N- (3,5-di-tert-butyl-4-hydroxyphenyl)carbamate.
  • esters of ⁇ -(3.5-di-tert-butyl-4-hydroxyphenyl)propionic acid with mono- or polyhydric alcohols e.g. with methanol, ethanol, n-octanol, i-octanol, octadecanol, 1 ,6-hexanediol, 1,9- nonanediol, ethylene glycol, 1 ,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethy ⁇ lene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl) isocyanurate, N,N'-bis(hy- droxyethyl)oxamide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylol ⁇ propane, 4-hydroxymethyl-1-phospha-2
  • esters of ⁇ - ( 5-tert-butyl-4-hvdroxy-3-methylphenvt propionic acid with mono- or poly ⁇ hydric alcohols e.g. with methanol, ethanol, n-octanol, i-octanol, octadecanol, 1,6-hexane- diol, 1,9-nonanediol, ethylene glycol, 1 ,2-propanediol, neopentyl glycol, thiodiethylene gly ⁇ col, diethylene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl) isocyanurate, N,N'-bis(hydroxyethyl)oxamide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylolpropane, 4-hydroxymethyl-1-phospha-2,6,
  • esters of ⁇ -(3.5-dicvclohexyl-4-hydroxyphenyl)propionic acid with mono- or polyhydric alcohols e.g. with methanol, ethanol, octanol, octadecanol, 1 ,6-hexanediol, 1 ,9-nonanediol, ethylene glycol, 1 ,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl)isocyanurate, N,N'-bis(hydroxyethyl)ox- amide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylolpropane, 4-hy- droxymethyl-1-phospha-2,6,7-trioxabicyclo[2.
  • esters of 3.5-di-tert-butyl-4-hvdroxyphenyl acetic acid with mono- or polyhydric alco ⁇ hols e.g. with methanol, ethanol, octanol, octadecanol, 1 ,6-hexanediol, 1 ,9-nonanediol, ethylene glycol, 1 ,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl)isocyanurate, N,N'-bis(hydroxyethyl)ox- amide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylolpropane, 4-hy- droxymethyl-1-phospha-2,6,7-trio
  • Aminic antioxidants for example N.N'-di-isopropyl-p-phenylenediamine, N,N'-di-sec- butyl-p-phenylenediamine, N,N'-bis(1 ,4-dimethylpentyl)-p-phenylenediamine, N,N'-bis(1 - ethyl-3-methylpentyl)-p-phenylenediamine, N,N'-bis(1-methylheptyl)-p-phenylenediamine, N.N'-dicyclohexyl-p-phenylenediamine, N.N'-diphenyl-p-phenylenediamine, N,N'-bis(2-naph- thyl)-p-phenylenediamine, N-isopropyl-N'-phenyl-p-phenylenediamine, N-(1 ,3-dimethylbutyl)- N
  • UV absorbers and light stabilisers 2.1. 2- ⁇ 2'-Hvdroxy p henyl)benzotriazoles. for example 2-(2'-hydroxy-5'-methylphenyl)-benzo- triazole, 2-(3',5 , -di-tert-butyl-2'-hydroxyphenyl)benzotriazole, 2-(5'-tert-butyl-2'-hydroxyphe- nyl)benzotriazole, 2-(2'-hydroxy-5'-(1 ,1 ,3,3-tetramethylbutyl)phenyl)benzotriazole, 2-(3',5'-di- tert-butyl-2'-hydroxyphenyl)-5-chloro-benzotriazole, 2-(3'-tert-butyl- 2'-hydroxy-5'-methylphe- nyl)-5-chloro-benzotriazole, 2-(3 , -sec-butyl-5'-tert-but
  • benzotriazol-2-ylphenyl 2-[2'-hydroxy-3'-( ⁇ , ⁇ -dimethylbenzyl)-5'-(1 ,1 ,3,3-tetramethylbutyl)- phenyl]benzotriazole; 2-[2'-hydroxy-3'-(1 ,1 ,3,3-tetramethylbutyl)-5'-( ⁇ , ⁇ -dimethylbenzyl)- phenyl]benzotriazole.
  • Esters of substituted and unsubstituted benzoic acids as for example 4-tertbutyl-phenyl salicylate, phenyl salicylate, octylphenyl salicylate, dibenzoyl resorcinol, bis(4-tert-butylben- zoyl) resorcinol, benzoyi resorcinol, 2,4-di-tert-butylphenyl 3,5-di-tert-butyl-4-hydroxybenzo- ate, hexadecyl 3,5-di-tert-butyl-4-hydroxybenzoate, octadecyl 3,5-di-tert-butyl-4-hydroxy- benzoate, 2-methyl-4,6-di-tert-butylphenyl 3,5-di-tert-butyl-4-hydroxybenzoate.
  • Nickel compounds for example nickel complexes of 2,2'-thio-bis-[4-(1 ,1 ,3,3-tetrame- thylbutyl)phenol], such as the 1 :1 or 1:2 complex, with or without additional ligands such as n-butylamine, triethanolamine or N-cyclohexyldiethanolamine, nickel dibutyldithiocarbamate, nickel salts of the monoalkyl esters, e.g. the methyl or ethyl ester, of 4-hydroxy-3,5-di-tert- butylbenzylphosphonic acid, nickel complexes of ketoximes, e.g. of 2-hydroxy-4-methylphe- nyl undecylketoxime, nickel complexes of 1 -phenyl-4-lauroyl-5-hydroxypyrazole, with or without additional ligands.
  • additional ligands such as n-butylamine, triethanolamine or N-cyclohexy
  • Sterically hindered amines for example bis(2,2,6,6-tetramethyl-4-piperidyl)sebacate, bis(2,2,6,6-tetramethyl-4-piperidyl)succinate, bis(1 , 2,2,6, 6-pentamethyl-4-piperidyl)seba- cate, bis(1-octyloxy-2,2,6,6-tetramethyl-4-piperidyl)sebacate, bis(1 ,2,2,6,6-pentamethyl-4-pi- peridyl) n-butyl-3,5-di-tert-butyl-4-hydroxybenzylmalonate, the condensate of 1 -(2-hydroxy- ethyl)-2,2,6,6-tetramethyl-4-hydroxypiperidine and succinic acid, linear or cyclic conden ⁇ sates of N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)hexamethylenedi
  • Oxamides for example 4,4'-dioctyloxyoxanilide, 2,2'-diethoxyoxanilide, 2,2'-dioctyloxy- 5,5'-di-tert-butoxanilide, 2,2 , -didodecyloxy-5,5'-di-tert-butoxanilide, 2-ethoxy-2'-ethyloxani- lide, N,N'-bis(3-dimethylaminopropyl)oxamide, 2-ethoxy-5-tert-butyl-2'-ethoxanilide and its mixture with 2-ethoxy-2'-ethyl-5,4'-di-tert-butoxanilide, mixtures of o- and p-methoxy-disub- stituted oxanilides and mixtures of o- and p-ethoxy-disubstituted oxanilides.
  • Metal deactivators for example N,N'-diphenyloxamide, N-salicylal-N'-salicyloyl hydrazine, N.N'-bis(salicyloyl) hydrazine, N,N'-bis(3,5-di-tert-butyl-4-hydroxyphenylpropionyl) hydrazine, 3-salicyloylamino-1 ,2,4-triazole, bis(benzylidene)oxalyl dihydrazide, oxanilide, isophthaloyi dihydrazide, sebacoyl bisphenylhydrazide, N,N'-diacetyladipoyl dihydrazide, N,N'-bis(salicyl- oyl)oxalyl dihydrazide, N,N'-bis(salicyloyl)thiopropionyl dihydrazide.
  • Phosphites and phosphonites for example triphenyl phosphite, diphenyl alkyl phosphites, phenyl dialkyl phosphites, tris(nonylphenyl) phosphite, trilauryl phosphite, trioctadecyl phos ⁇ phite, distearyl pentaerythritol diphosphite, tris(2,4-di-tert-butylphenyl) phosphite, diisodecyl pentaerythritol diphosphite, bis(2,4-di-tert-butylphenyl) pentaerythritol diphosphite, bis(2,6- di-tert-butyl-4-methylphenyl)-pentaerythritol diphosphite, diisodecyloxypentaerythritol di ⁇ phosphi
  • phosphites Especially preferred are the following phosphites:
  • Tris(2,4-di-tert-butylphenyl) phosphite (lrgafos*168, Ciba-Geigy), tris(nonylphenyl) phos ⁇ phite,
  • Hvdroxylamines for example, N,N-dibenzylhydroxylamine, N,N-diethylhydroxylamine, N,N-dioctylhydroxylamine, N,N-dilaurylhydroxylamine, N,N-ditetradecylhydroxylamine, N,N- dihexadecylhydroxylamine, N,N-dioctadecylhydroxylamine, N-hexadecyl-N-octadecylhy- droxylamine, N-heptadecyl-N-octadecylhydroxylamine, N,N-dialkylhydroxylamine derived from hydrogenated tallow amine.
  • Nitrones for example, N-benzyl-alpha-phenyl-nitrone, N-ethyl-alpha-methyl-nitrone, N-oc- tyl-alpha-heptyl-nitrone, N-lauryl-alpha-undecyl-nitrone, N-tetradecyl-alpha-tridcyl-nitrone, N- hexadecyl-aipha-pentadecyl-nitrone, N-octadecyl-alpha-heptadecyl-nitrone, N-hexadecyl- alpha-heptadecyl-nitrone, N-ocatadecyl-alpha-pentadecyl-nitrone, N-heptadecyl-alpha-hep- tadecyl-nitrone, N-octadecyl-alpha-hexadecyl-
  • Thiosyner ⁇ ists for example, dilauryl thiodipropionate or distearyl thiodipropionate.
  • Peroxide scaven ⁇ ers for example esters of ⁇ -thiodipropionic acid, for example the lauryl, stearyl, myristyl or tridecyl esters, mercaptobenzimidazole or the zinc salt of 2-mercapto- benzimidazole, zinc dibutyldithiocarbamate, dioctadecyl disulfide, pentaerythritol tetrakis( ⁇ - dodecylmercapto)propionate.
  • esters of ⁇ -thiodipropionic acid for example the lauryl, stearyl, myristyl or tridecyl esters, mercaptobenzimidazole or the zinc salt of 2-mercapto- benzimidazole, zinc dibutyldithiocarbamate, dioctadecyl disulfide, pentaerythritol tetrakis( ⁇ - dodecyl
  • Polyamide stabilisers for example, copper salts in combination with iodides and/or phos ⁇ phorus compounds and salts of divalent manganese.
  • Basic co-stabilisers for example, melamine, polyvinylpyrrolidone, dicyandiamide, triallyl cyanurate, urea derivatives, hydrazine derivatives, amines, polyamides, polyurethanes, al ⁇ kali metal salts and alkaline earth metal salts of higher fatty acids for example calcium stea ⁇ rate, zinc stearate, magnesium behenate, magnesium stearate, sodium ricinoleate and po ⁇ tassium palmitate, antimony pyrocatecholate or zink pyrocatecholate.
  • Basic co-stabilisers for example, melamine, polyvinylpyrrolidone, dicyandiamide, triallyl cyanurate, urea derivatives, hydrazine derivatives, amines, polyamides, polyurethanes, al ⁇ kali metal salts and alkaline earth metal salts of higher fatty acids for example calcium stea ⁇ rate, zinc stearate, magnesium
  • Nucleating agents for example, inorganic substances such as talcum, metal oxides such as titanium dioxide or magnesium oxide, phosphates, carbonates or sulfates of, pre ⁇ ferably, alkaline earth metals; organic compounds such as mono- or polycarboxylic acids and the salts thereof, e.g. 4-tert-butylbenzoic acid, adipic acid, diphenylacetic acid, sodium succinate or sodium benzoate; polymeric compounds such as ionic copolymers (ionomers).
  • inorganic substances such as talcum, metal oxides such as titanium dioxide or magnesium oxide, phosphates, carbonates or sulfates of, pre ⁇ ferably, alkaline earth metals
  • organic compounds such as mono- or polycarboxylic acids and the salts thereof, e.g. 4-tert-butylbenzoic acid, adipic acid, diphenylacetic acid, sodium succinate or sodium benzoate
  • polymeric compounds such as ionic copoly
  • Fillers and reinforcing agents for example, calcium carbonate, silicates, glass fibres, glass bulbs, asbestos, talc, kaolin, mica, barium sulfate, metal oxides and hydroxides, car ⁇ bon black, graphite, wood flour and flours or fibers of other natural products, synthetic fi ⁇ bers.
  • additives for example, plasticisers, lubricants, emulsifiers, pigments, rheology additives, catalysts, flow-control agents, optical brighteners, flameproofing agents, antistatic agents and blowing agents.
  • the additional additives and/or stabilizers are preferably added to the novel mixture compri ⁇ sing a) a secondary aromatic amine and b) a polyfunctional epoxide.
  • the additional additives are added to the polyolefin recyclate in concentrations, for example, of from 0.01 to 10 %, based on the overall weight of the polyolefin recyclate to be stabilized.
  • the fillers and reinforcing agents such as, for example, talc, calcium car ⁇ bonate, mica or kaolin, are added to the polyolefin recyclate in concentrations, for example, of from 0.01 to 40 %, based on the overall weight of the polyolefin recyclate to be stabilized.
  • the fillers and reinforcing agents such as, for example, metal hydroxides, especially aluminium hydroxide or magnesium hydroxide, are added to the polyolefin recyclate in concentrations, for example, of from 0.01 to 60 %, based on the overall weight of the polyolefin recyclate to be stabilized.
  • Carbon black as a filler is added to the polyolefin recyclate expediently in concentrations of from 0.01 to 5 %, based on the overall weight of the polyolefin to be stabilized.
  • Glass fibres as reinforcing agent are added to the polyolefin recyclate expediently in con ⁇ centrations of from 1 to 30 %, based on the overall weight of the polyolefin recyclate to be stabilized.
  • customary polyolefin additives can also be polymers which enhance the material properties of the previously damaged polyolefin, such as elastomers (impact modifiers) or compatibilizers (i.e. additives which improve compatibility).
  • elastomers impact modifiers
  • compatibilizers i.e. additives which improve compatibility
  • Impact modifiers are homo- or copolymers which are able to modify brittle polyolefins in such a way that they retain impact strength even in the cold. Suitable examples are EPM polymers, EPDM polymers, ABR, BR or SBR graft polymers.
  • compatibilizers examples include copolymers, especially block copolymers, of sty ⁇ rene with butadiene with or without acrylonitrile.
  • Further compatibilizers can be copolymers of ethylene and propylene with or without a third monomer component, such as butadiene, for example.
  • Chlorinated polyethylene, or ethylene-vinyl acetate copolymers are also sui ⁇ table as compatibilizers, a critical factor being of course the respective composition of the recyclate.
  • Further suitable compatibilizers contain, in particular, polar groups, for example maleic anhydride-styrene copolymers or graft polymers containing acrylic acid groups.
  • the compatibilizers are preferably used in amounts of from 2 to 20 %, based on the overall weight of the polyolefin recyclate to be stabilized.
  • further additives over and above at least one secondary aromatic amine and at least one polyfunctional epoxide are added, especial- ly UV absorbers and light stabilizers (item 2 in the list); amides of ⁇ -(3,5-di-tert-butyl-4-hy- droxyphenyl)propionic
  • Very special interest attaches to the novel process for stabilizing polyolefin recyclates against oxidative, thermal and/or light induced degradation wherein at least one compati ⁇ bilizer is added as a further additive in addition to at least one secondary aromatic amine and at least one polyfunctional epoxide.
  • the incorporation of the secondary aromatic amine and the polyfunctional epoxide, and of further additives if appropriate, into the polyolefin recyclate is accomplished by known methods, for example prior to or during shaping or else by applying the liquid, dissolved or dispersed stabilizer mixture to the polyolefin recyclate, with or without subsequent evapora ⁇ tion of the solvent.
  • the stabilizer mixture can also be added in the form of a masterbatch, containing said stabilizer mixture in a concentration, for example, of from 2.5 to 25 % by weight, based on the weight of the polyolefin recyclate or virgin polyolefin material, to the polyolefin recyclates which are to be stabilized.
  • novel stabilizer mixtures can be inco ⁇ orated in pure form or encapsulated in waxes, oils or polymers into the polyolefin recyclate which is to be stabilized.
  • novel stabilizers such as the secondary aromatic amine and the polyfunctional epoxide or mixtures thereof, can also be sprayed onto the polyolefin recyclate which is to be stabi ⁇ lized. They are capable of diluting other additives (for example the customary additives in ⁇ dicated above) and/or their melts, and consequently can also be sprayed together with these additives onto the polyolefin recyclate which is to be stabilized.
  • additives for example the customary additives in ⁇ dicated above
  • the polyolefin recyclates thus stabilized can be used for a very wide variety of purposes, for example for pipes, profiles and panels, such as insulating panels, pallets, cable insulation, sporting equipment, garden furniture, films, construction components, parts of vehicles and machines, containers of all kinds, such as bottles, or packaging material.
  • the polyolefin recyclate can also be employed in a form mixed with virgin polyolefin material or together with virgin material, for example in a coextrusion process.
  • the invention additionally provides for the use of a mixture comprising a secondary aroma ⁇ tic amine and a polyfunctional epoxide for stabilizing polyolefin recyclates against oxidative, thermal and/or light-induced degradation.
  • the preferences regarding the use correspond to those for the process.
  • the invention also provides a composition
  • a composition comprising a) a polyolefin recyclate, b) a secon ⁇ dary aromatic amine, and c) a polyfunctional epoxide.
  • the preferences regarding the com ⁇ position correspond to those for the process.
  • the invention additionally provides polyolefin recyclates obtainable by the novel process.
  • Example 1 Stabilizing polypropylene copolymer recyclate from battery cases.
  • regrind from used battery cases (polypropylene copolymer) is kneaded at a temperature of 210°C and at 40 revolu ⁇ tions/minute for 60 minutes together with the additives indicated in Table 1.
  • the torque of the polymer is determined after 30, 45 and 60 minutes. The greater the number, the better the stabilization.
  • the melt index (MFR) is measured (at 235°C under 2.16 kg in accordance with ISO 1 133). A large increase in the melt index denotes severe chain degradation, and therefore poor stabilization. The results are compiled in Table 1.
  • lrganox ⁇ 5057 (Ciba-Geigy) is 4,4'-di-tert-octyldiphenylamine (see formula Ie).
  • Araldit'GY 260 (Ciba-Geigy) is a liquid epoxide of the bisphenol A diglycidyl ether type.
  • Araldit'PY 306 (Ciba-Geigy) is a liquid epoxide of the bisphenol F diglycidyl ether type [diglycidyl ether of bis(ortho/para-hydroxyphenyl)methane (Bisphenol F)].
  • Araldit'GT 6071 (Ciba-Geigy) is bisphenol A diglycidyl ether with an epoxide number of 2.15-2.22 Eq/kg and a softening range of 70-75°C. e) Comparison examples. f) Novel examples.
  • Example 2 Stabilizing mixed polyolefin recyclates.
  • a mixture of used plastics consisting of about 80 % by weight of HD-polyethylene, about 15 % by weight of LD-poly- ethylene and about 5 % by weight of polypropylene is kneaded at a temperature of 190°C and at 40 revolutions/minute for 60 minutes together with the additives indicated in Table 2.
  • the torque of the polyolefin mixture is determined after 20, 40 and 60 minutes. The larger the number, the better the stabilization.
  • the melt index (MFR) is measured (at 235°C under 2.16 kg in accordance with ISO 1133). A large increase in the melt index denotes severe chain degradation, and thus poor stabilization. The results are compiled in Table 2.
  • lrganox ⁇ 5057 (Ciba-Geigy) is 4,4'-di-tert-octyldiphenylamine (see formula Ie).
  • Araldit'CY 179 (Ciba-Geigy) is liquid 3,4-epoxycyclohexylmethyl 3,4-epoxy- cyclohexanecarboxylate, epoxide content 7.0-7.5 equivalents/kg.
  • Araldit'EPN 1139 (Ciba-Geigy) is a liquid phenol novolak epoxy resin, epoxide content 5.6-6.8 equivalents/kg.
  • Comparison example e) Novel examples.

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Abstract

On peut stabiliser des produits de recyclage de polyoléfines, afin de les protéger contre la dégradation oxydative, thermique ou provoquée par la lumière, au moyen d'un apport d'au moins une amine aromatique secondaire et d'au moins une époxyde polyfonctionnelle.
PCT/EP1997/000497 1996-02-15 1997-02-04 Stabilisation de produits de recyclage de polyolefines WO1997030112A1 (fr)

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AU16005/97A AU1600597A (en) 1996-02-15 1997-02-04 Stabilisation of polyolefin-recyclates
JP9528943A JP2000506185A (ja) 1996-02-15 1997-02-04 ポリオレフィンリサイクル品の安定化
EP97902320A EP0880557A1 (fr) 1996-02-15 1997-02-04 Stabilisation de produits de recyclage de polyolefines

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EP1095978A1 (fr) * 1999-10-26 2001-05-02 Ciba SC Holding AG Mélange d'additifs pour améliorer les charactéristiques mécaniques des polymères
WO2013068395A1 (fr) 2011-11-09 2013-05-16 Basf Se Polymères à base de polyoléfines greffées
US8987368B2 (en) 2011-11-09 2015-03-24 Basf Se Polymers based on grafted polyolefins
DE102017217312A1 (de) 2017-09-28 2019-03-28 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Verfahren zur Stabilisierung von halogenfreien thermoplastischen Kunststoff-Rezyklaten sowie stabilisierte Kunststoffzusammensetzungen und hieraus hergestellte Formmassen und Formteile
DE102019200905A1 (de) 2019-01-24 2020-07-30 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Verfahren zur Stabilisierung von halogenfreien thermoplastischen Kunststoff-Rezyklaten, Kunststoff-Zusammensetzung, Stabilisator-Zusammensetzung sowie Verwendung der Stabilisator-Zusammensetzung
WO2020193563A1 (fr) 2019-03-26 2020-10-01 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Procédé pour stabiliser des produits recyclés à base de matières plastiques thermoplastiques et compositions de matières plastiques stabilisées ainsi que masses à mouler et pièces moulées fabriquées à partir de celles-ci
US10975228B2 (en) 2015-06-15 2021-04-13 Imertech Sas Compositions for injection moulding
DE102021202103A1 (de) 2021-03-04 2022-09-08 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung eingetragener Verein Verwendung einer Stabilisatorzusammensetzung zur Stabilisierung von halogenfreien thermoplastischen Kunststoff-Recyclaten, eine Stabilisatorzusammensetzung, ein Masterbatch oder Konzentrat, eine stabilisierte Kunststoffzusammensetzung, hier ein Verfahren zur Stabilisierung von halogenfreien thermoplastischen Kunststoff-Recyclaten sowie Verwendung von Zusammensetzungen
DE102021202508A1 (de) 2021-03-15 2022-09-15 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung eingetragener Verein Verwendung einer Stabilisatorzusammensetzung zur Stabilisierung von Polyolefin-Recyclaten, Stabilisatorzusammensetzung, Masterbatchkonzentrat, Kunststoffzusammensetzung, Formmasse oder Formteil, Verfahren zur Stabilisierung eines Polyolefin-Recyclats sowie Verwendung einer Kunststoffzusammensetzung
DE102021205168A1 (de) 2021-05-20 2022-11-24 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung eingetragener Verein Verwendung mindestens einer Schwefel enthaltenden Aminosäure zur Stabilisierung von thermoplastischen Kunststoff-Recyclaten, stabilisiertes thermo-plastisches Kunststoffrecyclat, Stabilisatorzusammensetzung, Masterbatch sowie Formmasse bzw. Formteil
WO2025114330A1 (fr) 2023-11-29 2025-06-05 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Utilisation d'amines secondaires et/ou tertiaires aliphatiques linéaires ou ramifiées, pour la stabilisation de matières thermoplastiques exemptes d'halogènes, de préférence de matières plastiques recyclées, contre la dégradation oxydative, thermique ou actinique, composition de matière thermoplastique, procédé de stabilisation

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US12398256B2 (en) 2019-03-26 2025-08-26 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Method for stabilizing thermoplastic recyclates, stabilized plastic compositions, and molding compounds and molded parts produced therefrom
WO2022184596A1 (fr) 2021-03-04 2022-09-09 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Utilisation d'une composition stabilisante pour stabiliser des thermoplastiques recyclés exempts d'halogène, composition stabilisante, mélange maître ou concentré, composition de plastique stabilisée, procédé de stabilisation de thermoplastiques recyclés exempts d'halogène et utilisation des compositions
DE102021202103A1 (de) 2021-03-04 2022-09-08 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung eingetragener Verein Verwendung einer Stabilisatorzusammensetzung zur Stabilisierung von halogenfreien thermoplastischen Kunststoff-Recyclaten, eine Stabilisatorzusammensetzung, ein Masterbatch oder Konzentrat, eine stabilisierte Kunststoffzusammensetzung, hier ein Verfahren zur Stabilisierung von halogenfreien thermoplastischen Kunststoff-Recyclaten sowie Verwendung von Zusammensetzungen
DE102021202508A1 (de) 2021-03-15 2022-09-15 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung eingetragener Verein Verwendung einer Stabilisatorzusammensetzung zur Stabilisierung von Polyolefin-Recyclaten, Stabilisatorzusammensetzung, Masterbatchkonzentrat, Kunststoffzusammensetzung, Formmasse oder Formteil, Verfahren zur Stabilisierung eines Polyolefin-Recyclats sowie Verwendung einer Kunststoffzusammensetzung
WO2022194672A1 (fr) 2021-03-15 2022-09-22 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Utilisation d'une composition stabilisante pour stabiliser des recyclats de polyoléfine, composition de stabilisant, concentré de mélange maître, composition de matière plastique, composé de moulage ou moulage, procédé de stabilisation recyclat de polyoléfine et utilisation d'une composition de matière plastique
DE102021205168A1 (de) 2021-05-20 2022-11-24 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung eingetragener Verein Verwendung mindestens einer Schwefel enthaltenden Aminosäure zur Stabilisierung von thermoplastischen Kunststoff-Recyclaten, stabilisiertes thermo-plastisches Kunststoffrecyclat, Stabilisatorzusammensetzung, Masterbatch sowie Formmasse bzw. Formteil
WO2022243354A1 (fr) 2021-05-20 2022-11-24 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Utilisation d'au moins un acide aminé soufré pour stabiliser des thermoplastiques recyclés, thermoplastique recyclé stabilisé, composition stabilisante, mélange-maître et matière à mouler ou pièce moulée
WO2025114330A1 (fr) 2023-11-29 2025-06-05 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Utilisation d'amines secondaires et/ou tertiaires aliphatiques linéaires ou ramifiées, pour la stabilisation de matières thermoplastiques exemptes d'halogènes, de préférence de matières plastiques recyclées, contre la dégradation oxydative, thermique ou actinique, composition de matière thermoplastique, procédé de stabilisation

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JP2000506185A (ja) 2000-05-23
AU1600597A (en) 1997-09-02
CA2243697A1 (fr) 1997-08-21
TW364911B (en) 1999-07-21

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