EP2635636A1 - Matières moulables en polycarbonate protégées contre les uv et ignifuges, ayant un poids moléculaire à faible dégradation - Google Patents

Matières moulables en polycarbonate protégées contre les uv et ignifuges, ayant un poids moléculaire à faible dégradation

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Publication number
EP2635636A1
EP2635636A1 EP11778591.5A EP11778591A EP2635636A1 EP 2635636 A1 EP2635636 A1 EP 2635636A1 EP 11778591 A EP11778591 A EP 11778591A EP 2635636 A1 EP2635636 A1 EP 2635636A1
Authority
EP
European Patent Office
Prior art keywords
polycarbonate
free
less
absorber
flame
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP11778591.5A
Other languages
German (de)
English (en)
Inventor
Berit Krauter
Michael Wagner
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.)
Bayer Intellectual Property GmbH
Original Assignee
Bayer Intellectual Property GmbH
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 Bayer Intellectual Property GmbH filed Critical Bayer Intellectual Property GmbH
Priority to EP11778591.5A priority Critical patent/EP2635636A1/fr
Publication of EP2635636A1 publication Critical patent/EP2635636A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
    • 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
    • C08K5/41—Compounds containing sulfur bound to oxygen
    • C08K5/42—Sulfonic acids; Derivatives thereof
    • 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
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3472—Five-membered rings
    • C08K5/3475—Five-membered rings condensed with carbocyclic 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
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3477—Six-membered rings
    • C08K5/3492—Triazines

Definitions

  • the present invention relates to flame-retardant, UV-resistant polycarbonate molding compositions, with improved flame retardancy and a low incorporation of the UV absorber into the polymer chain and a resulting compared to the polycarbonates with increased incorporation of UV radiation.
  • plastics such as e.g. Transparency, toughness and low density paired with thermoplastic ductility, which ensures high design freedom, are increasingly replacing plastics with metal as a material from various applications. This happens especially where weight reduction comes to the fore.
  • materials are mainly used in aircraft construction, but also in rail transport or automotive engineering.
  • plastics are also used in IT and electrical engineering and electronics, where they are used e.g. be used as a carrier of live parts or for the production of television and monitor housings. For the aforementioned applications, it is necessary in many cases that the used
  • Plastics in addition to good mechanical properties also have increased flame retardance and good resistance to UV rays.
  • suitable additives such as flame retardants and UV stabilizers, must be added to the plastics that are generally combustible.
  • flame retardants and UV stabilizers must be added to the plastics that are generally combustible.
  • the addition of these additives not only brings the desired benefits. That is how it is
  • Lower molecular weight polycarbonates also tend to have inferior mechanical properties. Short-chain polycarbonates are more prone to burning droplets in the UL94V test than long-chain ones. Thus, the molecular weight degradation caused by the esterification of the UV absorber also gives a negative influence on the flame retardancy. This described problem also exists for polycarbonate compositions which are flame-retardant with the aid of alkali or alkaline-earth salts, since here the poor dripping behavior is primarily responsible for a negative evaluation in the flame retardancy test.
  • EP 1 770 126 A1 describes aromatic polycarbonate compositions having good flame retardancy and improved fire dripping behavior.
  • the compositions contain aromatic polycarbonate, a salt of a fluorinated organic acid containing free fluoride in a proportion of 0.2-20 ppm, and at least one other additive.
  • EP 1 770 126 A1 discloses compositions according to the present invention comprising polycarbonate, flame retardant and reactive UV stabilizer which contain fluoride and sulfate in the given amounts and a reduced incorporation of the reactive UV absorber and improved stability (low relative) Viscosity), not described.
  • JP 06 299057 halogen-containing aromatic polycarbonate compounds are described which improve their transparency, flame properties and impact resistance by the addition of alkali metal salts.
  • Polycarbonates with various alkali metal or alkaline earth sulfonates as flame retardants are known and described inter alia in US Pat. No. 3,933,734, US Pat. No. 3,940,366, US Pat. No. 3,953,399, US Pat. No. 3,926,908, US Pat. No. 4,104,246 and EP392,252.
  • US 2003/0069338 discloses flame-retardant molding compositions containing synergistic combinations of cyanoacrylates and flame retardants.
  • the molding compositions thus treated are distinguished by improved flame retardance and improved weathering stability.
  • WO 2008/125203 A1 describes a composition comprising polycarbonate and 2- [2-hydroxy-4- (2-ethylhexyl) oxy] phenyl-4,6-di (4-phenyl) phenyl-1,3,5-triazine as UV absorber in combination with flame retardant additives.
  • the object of the present invention is therefore to provide UV-protected, flame-retardant polycarbonate molding compositions with less polymer degradation and resulting improved flame retardancy, in comparison to the polycarbonates with increased incorporation of UV absorbers of higher relative solution viscosity and improved mechanical properties.
  • the relative solution viscosity should be at most 2.00%, preferably at most 1.50%, more preferably at most 1.30%, and most preferably at most 1.10% lower than the relative solution viscosity for the preparation of the respective overall composition used pure, not with component B) and C) additized polycarbonate (corresponding to 100% component A) in the overall composition).
  • polycarbonates which contain as flame retardants alkali metal or alkaline earth metal salts of fluorinated organic acids in combination with at least one UV absorber, and which show a significantly reduced degradation of the polymer chain, preferably more than 50 wt % of the UV absorber originally used is freely present in the polycarbonate and is not incorporated into the polymer chain.
  • composition comprising at least one polycarbonate, at least one alkali metal or alkaline earth metal salt of fluorinated organic acids as flame retardants and at least one reactive UV absorber, wherein the alkali metal or alkaline earth metal salt (component C)) contains a proportion of sulfate less than 0.007 wt .-% and preferably additionally has a content of free fluoride of less than 0.017 wt .-%, each based on the total mass of component C).
  • the polycarbonates are used in the context of the present inventions as component A) in amounts of 99.998% to 98,000% by weight, preferably 99.949% to 98.400% by weight, more preferably 99.890% to 98.900% by weight and even more preferably 99.790% by weight. % to 99.300 wt .-%, and particularly preferably from 99.780 wt .-% to 99.400 wt -.%, Each based on the total composition used.
  • the UV absorbers as component B) are used in the context of the present invention in amounts of from 0.001% by weight to 1,000% by weight, preferably from 0.050% by weight to 0.800% by weight, more preferably 0, 100% by weight. % to 0.500 wt .-%, and particularly preferably 0.200 wt .-% to 0.400 wt .-%, each based on the total composition used.
  • the alkali metal or alkaline earth metal salts are used in the context of the present invention as component C) in amounts of from 0.001% by weight to 1,000% by weight, preferably from 0.001% by weight to 0.800% by weight, more preferably 0.010% by weight. to 0.600 wt .-%, and more preferably 0.010 wt .-% to 0.300 wt .-%, and particularly preferably 0.020 wt .-% to 0.200 wt .-%, each based on the total composition used in the molding compositions.
  • the sum of the components AC add up to 100.
  • Alkaline or alkaline earth metal salts in the context of the present invention are derived from aliphatic or aromatic sulfonic acid sulfonamide and sulfonimide derivatives.
  • Potassium perfluoro-1-butanesulfonate is commercially available inter alia as Bayowet® C4 from Lanxess, Leverkusen, Germany.
  • Suitable UV absorbers in the context of the present invention are compounds of the formula (I), it also being possible to use mixtures of differently substituted compounds,
  • R 1 and R 2 are the same or different and are H, halogen, C 1 to C 10 alkyl, C 5 to C 10 cycloalkyl, C 7 to C 13 aralkyl
  • R5 is H or Cl - to C4-alkyl
  • R3 and R4 are the same or different and are H, C1 to C4 alkyl, C5 to C6 cycloalkyl, benzyl or C6 to C14 aryl, m is 1, 2 or 3 and n is 1, 2, 3 or 4 is.
  • UV absorbers are compounds of the formula (II) and also mixtures which are substituted in different ways,
  • R and X are identical or different and are H or alkyl or alkylaryl
  • UV absorbers are compounds of the formula (III) and also mixtures which are substituted in different ways,
  • R 1 and R 2 are identical or different and are H, halogen, C 1 - to C 10 -alkyl, C 5 - to C 10 -cycloalkyl, C 7 - to C 13 -aralkyl,
  • R5 is H or Cl - to C4-alkyl, m is 1, 2 or 3 and n is 1, 2, 3 or 4,
  • Y is -CH 2 -CH 2 -, - (CH 2) 3, - (CH 2) 4, - (CH 2) 5, - (CH 2) 6, or CH (CH 3) -CH 2 -and and
  • R 10 and R 11 are identical or different and denote H, C 1 - to C 4 -alkyl, C 5 - to C 6 -cycloalkyl, benzyl or C 6 - to C 14 -aryl.
  • R 10 and R 11 are identical or different and denote H, C 1 - to C 4 -alkyl, C 5 - to C 6 -cycloalkyl, benzyl or C 6 - to C 14 -aryl.
  • those are preferred
  • the compounds of formula (I), (II) and (III) to be used according to the invention are commercially available. They can be prepared by known methods.
  • Compounds of formula (II) are 2- (2-hydroxy-5-tert-octylphenyl) -2H-benzotriazole (Tinuvin® 329), 2- (2H-benzotriazol-2-yl) -4- (1,1-dimethylethyl ) -6- (2-methylpropyl) phenol (Tinuvin® 350) or 2- [2'-hydroxy-3,5-di (1,1-dimethylbenzyl) phenyl] -2H-benzotriazole (Tinuvin® 234).
  • the Tinuvines are available from BASF AG, Ludwigshafen, Germany (formerly available from Ciba Spezimaschineenchemie, Lampertheim, Germany).
  • UV absorbers based on triazines Furthermore, it is also possible to use UV absorbers based on triazines.
  • Suitable polycarbonates for the production of the plastic composition according to the invention are all known polycarbonates. These are homopolycarbonates, copolycarbonates and thermoplastic polyestercarbonates.
  • the suitable polycarbonates preferably have average molecular weights M w of from 18,000 to 40,000 g / mol, preferably from 22,000 to 31,000 g / mol and especially from 26,000 to 28,000 g / mol, determined by measuring the relative solution viscosity in dichloromethane (versus polycarbonate standard) at one concentration of 5 g / 1 and a temperature of 25 ° C with an Ubbelohde viscometer.
  • the preparation of the polycarbonates is preferably carried out by the interfacial process or the melt transesterification process, which are described in various ways in the literature.
  • interfacial process see, for example, H. Schnell, Chemistry and Physics of Polycarbonates, Polymer Reviews, Vol. 9, Interscience Publishers, New York 1964, p. 33 et seq., Polymer Reviews, Vol. 10, "Condensation Polymers by Interfacial and Solution Methods". , Paul W. Morgan, Interscience Publishers, New York 1965, Chapter VIII, p. 325, to Dres. U. Grigo, K. Kircher and P.
  • melt transesterification process is described, for example, in the Encyclopedia of Polymer Science, Vol. 10 (1969), Chemistry and Physics of Polycarbonates, Polymer Reviews, H. Schnell, Vol. 9, John Wiley and Sons, Inc. (1964) and in US Pat Patent DE-B 10 31 512 and US-B 6 228 973 described.
  • the polycarbonates are obtained from reactions of bisphenol compound with carbonic acid compounds, in particular phosgene, or in the melt transesterification process, diphenyl carbonate or dimethyl carbonate. Homopolycarbonates based on bisphenol A and copolycarbonates based on the monomers bisphenol A and 1,1-bis (4-hydroxyphenyl) -3,3,5-trimethylcyclohexane are particularly preferred. Other bisphenol compounds which can be used for the polycarbonate synthesis are disclosed inter alia in WO-A 2008037364, EP-A 1 582 549, WO-A 2002026862, WO-A 2005113639
  • the polycarbonates may be linear or branched. Mixtures of branched and unbranched polycarbonates can also be used.
  • Suitable branching agents for polycarbonates are known from the literature and described for example in the patents US-B 4 185 009, DE-A 25 00 092, DE-A 42 40 313, DE-A 19 943 642, US-B 5 367 044 and US Pat in literature cited herein.
  • the polycarbonates used can also be intrinsically branched, in which case no branching agent is added during the polycarbonate production.
  • An example of intrinsic branches are so-called frieze structures, as disclosed for melt polycarbonates in EP-A 1 506 249.
  • the polycarbonates and copolycarbonates according to the invention may also contain other aromatic polycarbonates and / or other plastics such as aromatic polyester carbonates, aromatic polyesters such as polybutylene terephthalate or polyethylene terephthalate, polyamides, polyimides, polyesteramides, polyacrylates and polymethacrylates such as, for example, polyalkyl (meth) acrylates and in particular polymethyl methacrylate, polyacetals, Polyurethanes, polyolefins, halogen-containing polymers, polysulfones, polyethersulfones, polyetherketones, polysiloxanes, polybenzimidazoles, urea-formaldehyde resins, melamine-formaldehyde resins, phenol-formaldehyde resins,
  • Alkyd resins epoxy resins, polystyrenes, copolymers of styrene or of alpha-methylstyrene with dienes or acrylic derivatives, graft polymers based on acrylonitrile / butadiene / styrene or graft copolymers based on acrylate rubber (see, for example, the graft polymers described in EP-A 640 655) or silicone rubbers in be admixed known manner, for example by compounding.
  • polycarbonates according to the invention and any further plastics contained may also be added in conventional amounts for the customary additives for these thermoplastics, such as fillers, thermal stabilizers, antistatic agents and pigments; if necessary, the demolding behavior or the flow behavior can be improved by adding external mold release agents, or flow agents (eg., Alkyl- and aryl phosphites, phosphates, phosphanes, - low molecular weight carboxylic acid esters, halogen compounds, salts, chalk, quartz powder, glass and Carbon fibers, pigments and their combination). Such compounds are z. In WO 99/55772, pages 15-25, EP 1 308 084 and in the corresponding chapters of the "Plastics Additives Handbook", ed.
  • composition containing polycarbonate and said additives is carried out by conventional incorporation methods and can be, for example, by mixing solutions of the additives and solution of polycarbonate in suitable solvents such as dichloromethane, haloalkanes, haloaromatics, chlorobenzene and xylenes.
  • suitable solvents such as dichloromethane, haloalkanes, haloaromatics, chlorobenzene and xylenes.
  • the solution mixtures are preferably worked up in a known manner by evaporation of the solvent and subsequent extrusion, for example, compounded.
  • composition can be mixed in conventional mixing devices such as screw extruders (for example twin-screw extruder, ZSK), kneaders, Brabender or Banbury mills and then extruded. After extrusion, the extrudate can be cooled and comminuted. It is also possible to premix individual components and then to add the remaining starting materials individually and / or likewise mixed.
  • compositions according to the invention can be worked up in a known manner and processed to give any shaped bodies, for example by extrusion, injection molding or extrusion blow molding.
  • the content of sulfate and free fluoride was determined according to DIN-ISO 17025.
  • the solution viscosities were determined according to the DIN ISO 1628 standards.
  • the content of free Tinuvin was determined by UV / Vis spectroscopy.
  • Tinuvin 329 is detected at the two wavelengths 300 nm for the total amount used and at 340 nm for the free portion of the tinuvin.
  • the incorporated amount of TIN 329 was determined from the difference of the products from the UV intensities at 300nm multiplied by the factor 2, 16 and at 340nm multiplied by the factor 1.96. The factors were determined by calibration.
  • Eta-rel The relative solution viscosity Eta rel is determined in methylene chloride (0.5 g polycarbonate / 1) at 25 ° C. in an Ubbelohde viscometer.
  • Makrolon ® 2808 is a commercially available linear polycarbonate based on bisphenol A from Bayer Material Science AG. Makroion ® 2808 contains no UV absorber. The melt volume flow rate (MVR) according to ISO 1133 is 9.5 cm7 (10 min) at 300 ° C and 1.2 kg load.
  • Tinuvin ® 329 is a 2- (2H-benzotriazol-2-yl) -4- (l, l, 3,3-tetramethylbutyl) phenol and as Tinuvin ® (329 CAS No. 3147-75-9) the company BASF AG, Ludwigshafen, Germany (formerly available from the company Ciba Spezilticianenchemie, Lampertheim, Germany) commercially available,
  • potassium perfluoro-l-butane sulfonate and example as Bayowet ® C4 from Lanxess, Leverkusen, Germany, CAS-No. 29420-49-3 are currently available. Potassium perfluorobutanesulfonates with different fluorine and sulfate contents were used. These potassium perfluorobutanesulfonates are preferably to be prepared by doping de s by repeated recrystallization purified flame retardant.
  • compositions according to the invention have a high content and free UV absorber and a higher relative solution viscosity.

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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)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

La présente invention concerne des matières moulables en polycarbonate résistantes aux ultraviolets et protégées contre les flammes, ayant une aptitude de non propagation de la flamme améliorée et une faible incorporation d'absorbeurs d'UV dans la chaîne polymérique et, par conséquent, une viscosité relative supérieure comparé aux polycarbonates ayant une incorporation accrue d'absorbeurs d'UV. Les compositions de polycarbonate contiennent A) au moins un polycarbonate ayant un poids moléculaire moyen (a) de 18.000 à 40.000 g/mol, B) au moins un absorbeur d'UV réactif et, C) au moins un sel alcalin ou alcalino-terreux d'un acide organique fluoré et C) une fraction d'un sulfate libre inférieur à 0,007 % en poids et une teneur en un fluorure libre inférieur à 0,017 % en poids respectivement par rapport à la masse de C).
EP11778591.5A 2010-11-05 2011-11-03 Matières moulables en polycarbonate protégées contre les uv et ignifuges, ayant un poids moléculaire à faible dégradation Withdrawn EP2635636A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP11778591.5A EP2635636A1 (fr) 2010-11-05 2011-11-03 Matières moulables en polycarbonate protégées contre les uv et ignifuges, ayant un poids moléculaire à faible dégradation

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP10190144 2010-11-05
PCT/EP2011/069289 WO2012059528A1 (fr) 2010-11-05 2011-11-03 Matières moulables en polycarbonate protégées contre les uv et ignifuges, ayant un poids moléculaire à faible dégradation
EP11778591.5A EP2635636A1 (fr) 2010-11-05 2011-11-03 Matières moulables en polycarbonate protégées contre les uv et ignifuges, ayant un poids moléculaire à faible dégradation

Publications (1)

Publication Number Publication Date
EP2635636A1 true EP2635636A1 (fr) 2013-09-11

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EP11778591.5A Withdrawn EP2635636A1 (fr) 2010-11-05 2011-11-03 Matières moulables en polycarbonate protégées contre les uv et ignifuges, ayant un poids moléculaire à faible dégradation

Country Status (5)

Country Link
US (1) US9193848B2 (fr)
EP (1) EP2635636A1 (fr)
KR (1) KR101838994B1 (fr)
CN (1) CN103391970B (fr)
WO (1) WO2012059528A1 (fr)

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CN106188652A (zh) * 2016-07-08 2016-12-07 广安奥海通讯电子科技有限公司 一种显示屏外壳材料

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Also Published As

Publication number Publication date
CN103391970B (zh) 2015-03-25
KR20130143071A (ko) 2013-12-30
KR101838994B1 (ko) 2018-03-15
US20130245165A1 (en) 2013-09-19
WO2012059528A1 (fr) 2012-05-10
CN103391970A (zh) 2013-11-13
US9193848B2 (en) 2015-11-24

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