WO2000073386A1 - Matieres a mouler en polycarbonate servant a la realisation de produits attirant peu la poussiere - Google Patents
Matieres a mouler en polycarbonate servant a la realisation de produits attirant peu la poussiere Download PDFInfo
- Publication number
- WO2000073386A1 WO2000073386A1 PCT/EP2000/004573 EP0004573W WO0073386A1 WO 2000073386 A1 WO2000073386 A1 WO 2000073386A1 EP 0004573 W EP0004573 W EP 0004573W WO 0073386 A1 WO0073386 A1 WO 0073386A1
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- WIPO (PCT)
- Prior art keywords
- molding compositions
- compositions according
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- hydroxyphenyl
- tert
- Prior art date
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Classifications
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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
- C08K5/0008—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
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
-
- 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
-
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
Definitions
- the invention relates to transparent polycarbonate molding compositions for plastic articles which contain at least one thermal stabilizer and a mold release agent and which have a lower tendency to accumulate dust.
- a known method to reduce dust accumulation on plastic bodies is through the use of antistatic agents.
- Antistatic agents are described in the literature for thermoplastics (see e.g. Gumbleter, Müller, Plastic Additives, Hanser Verlag, Kunststoff, 1996, p. 749 ff), which restrict dust accumulation. These antistatic agents improve the electrical conductivity of the plastic molding compounds and thus dissipate surface charges that form during manufacture and use. As a result, dust particles are no longer attracted and consequently there is less dust accumulation.
- Antistatic is applied to the molded plastic body after processing, an internal antistatic is added as an additive during processing.
- an internal antistatic agent is usually desirable, since no further steps are necessary to apply the antistatic agent after processing. So far, however, no internal antistatic has been known for transparent settings of polycarbonate, which effectively limits the accumulation of dust and at the same time does not impair the advantageous properties of this material such as high transparency, low haze and high impact strength.
- a disadvantage of adding antistatic agents is that, like any additive added, they increase the production cost of an article. Therefore, it would generally be desirable to use as few additives (number and amount) as possible.
- thermoplastic molding composition which, as an amorphous thermoplastic polymer, contains polycarbonate and at least one antioxidant and a mold release agent, the antioxidant comprising at least one stabilizer from the group TPP, tetrakis (2,4-di-tert-butylphenyl) -4,4'-biphenylene-diphosphonite, Irganox 1222, octadecyl-3- (3 ', 5 ' -di-tert-butyl-4'-hydroxyphenyl) propionate, Irganox ® HP2921, Anox ® TB331, TB123 Anox ® or a mixture thereof, preferably in amounts 0001-1 wt .-%, more preferably is between 0.01 and 0.1 wt .-% contains
- the mold release agent at least one substance from the group
- polyols preferably glycerol, ethylene glycol, propylene glycol, pentaerythritol, dipentaerythritol or tripentaerythritol or fatty alcohols are used.
- Carboxylic acids in particular fatty acids, such as stearic acid or palmitic acid, and mixtures thereof are particularly preferred. Unsaturated fatty acids can optionally also be hydrogenated or epoxidized.
- Suitable end groups are branched or unbranched carboxylic acids having 1-30 carbon atoms, which can also be completely or partially fluorinated.
- esters of trimellitic acid are particularly preferred.
- GMS glycerol monostearate
- triglycerides such as Grinstedt ® PS 102 (Danisco, Braband, Denmark)
- Pentaerythritol tetrastearate PETS
- polyol fatty acid esters such as Loxiol ® EP218 (Henkel KG, Düsseldorf, Germany)
- isocetyl stearyl stearate, 1,3-propanediol esterified with natural fatty acid such as Grinstedt ® PGMS SPV (Danisco, Braband, Denmark)
- epoxidized oils such as soybean oil or linseed oil, which, for example under the name Edenol ® B35 and B316 from Henkel KG, Dusseldorf, Germany, buy, and trimellitic of monocarboxylic acids such as Edenol ® W31 OS Henkel KG, Dusseldorf, Germany.
- Mixtures of the mold release agents described above are also very particularly preferred.
- the mold release agents are preferred in amounts of between 0.001 each
- % By weight and 5% by weight, preferably 0.01% by weight and 1% by weight, preferably between 0.1-1% by weight and very particularly preferably between 0.2 and 0.6% by weight.
- Antioxidants suitable according to the invention are e.g. in EP 0 839 623 AI and EP
- Triarylphosphines such as triphenylphosphine (TPP) or aromatic phosphine substituted with linear or branched alkyl chains with 1-30 C atoms are particularly suitable.
- aliphatic or aromatic phosphites such as, for example, tris (2,4-di-tert.butylphenyl) phosphite, hindered phenols, such as, for example, ocadecyl-3- (3 ' , 5 ' -di-tert-butyl-4 ' Hydroxyphenyl) propionate, other compounds such as thioethers, for example distearyl 3,3 ' thiodipropionate, organic phosphates such as TOF (tris (2-ethylhexyl) phosphate), silicones such as Dynasilan ® Glymo, and mixtures thereof.
- TOF tris (2-ethylhexyl) phosphate
- silicones such as Dynas
- triphenylphosphine Irganox ® 1222 (diethyl ((3,5-bis (l, l-dimethylethyl) -4-hydroxyphenyl) methyl) phosphonate product of Ciba Specialty Chemicals Basel), tetrakis (2,4-di tert-butylphenyl) -4,4'-biphenylene diphosphonite (Irgafos ® PEPQ), octadecyl-3- (3 ', 5 ' -di-tert-butyl-4'-hydroxyphenyl) propionate (Irganox ® 1076), Tris (2,4-di-tert-butyl-phenyl) phosphite (Irgafos ® 168) and Anox ® TB123 (mixture of octadecyl-3- (3 ', 5'-di-tert-buty
- Anox ® TB331 (mixture of Tris (2,4-di-tert-butyl-4-hydroxyhydrocinnamate) methane, tris (2,4-di-tert-butyl-phenyl) phosphite and distearyl-3,3'-thiodipropionate) (product of the Great Lakes Chemical Corp.
- Irganox ® HP2921 mixture of octadecyl 3- (3 ', 5' -di-tert-butyl-4 '- hydroxyphenyl) propionate, tris (2,4-di- tert-butyl ph enyl) phosphite and Irganox ® HP136 5,7-di-tert-butyl-3- (3,4-dimethylphenyl) -2 (3H) -benzofuranone (product of Ciba Specialty Chemicals, Basel).
- the antioxidants are preferably used in amounts of between 0.001% by weight and 10% by weight, preferably between 0.01% by weight and 0.1% by weight and very particularly preferably between 0.02 and 0.06% by weight.
- suitable UV absorbers are also optionally added, these are e.g. in EP 0 839 623 AI and EP 0 500 496.
- hydroxy-benzotriazoles such as 2- (3 ', 5-'Bis- (l, l-dimethylbenzyl) -2' hydroxy-phenyl) benzotriazole (Tinuvin 234, Ciba Specialty Chemicals, Basel), 2- (2'-Hydroxy-5 '- (tert-octyl) phenyl) benzotriazole (Tinuvin ® 329, Ciba Specialty Chemicals, Basel), 2- (2'-Hydroxy-3' - (2-butyl) -5 ' -
- (tert-butyl) phenyl) benzotriazole (Tinuvin ® 350, Ciba Specialty Chemicals, Basel), Bis- (3- (2H-benzotriazolyl) -2-hydroxy-5-tert-octyl) methane, (Tinuvin ® 360, Ciba Specialty Chemicals, Basel), 2- (4-hexoxy-2-hydroxyphenyl) -4,6- diphenyl-l, 3,5-triazine (Tinuvin 1577, Ciba Specialty Chemicals, Basel), and the benzophenone 2,4-dihydroxy-benzophenone (Chimasorb22 ® , Ciba Specialty Chemicals, Basel).
- the UV absorbers are preferred in amounts of in each case between 0.001% by weight and 10% by weight, preferably 0.01% by weight and 1% by weight, preferably between 0.1-1% by weight and very particularly preferably between 0.2 and 0.6 wt .-% used.
- additives can be used, e.g. Flame retardants, fillers, foaming agents, dyes, pigments, optical brighteners and nucleating agents or the like known from the literature, preferably in amounts of up to 5% by weight, preferably 0.01 to 5% by weight, based on the mixture as a whole, particularly preferred 0.01 wt .-% to 1 wt .-% based on the amount of plastic is included. Mixtures of these additives are also suitable.
- Transparent thermoplastics are preferably used as the transparent plastic, particularly preferably the polymers of ethylenically unsaturated monomers and / or polycondensates of bifunctional reactive compounds.
- plastics are polycarbonates or copolycarbonates based on diphenols, the poly- or copolyacrylates and poly- or copolymethacrylates such as poly- or copolymethyl methacrylate, also as copolymers with styrene such as transparent polystyrene-acrylonitrile (SAN), furthermore transparent cycloolefms, Poly- or copolycondensates of terephthalic acid, such as poly- or copolyethylene terephthalate (PET or CoPET) or glycol-modified PET (PETG).
- SAN transparent polystyrene-acrylonitrile
- PET poly- or copolyethylene terephthalate
- PET glycol-modified PET
- Thermoplastic, aromatic polycarbonates in the sense of the present invention are both homopolycarbonates and copolycarbonates; the polycarbonates can be linear or branched in a known manner.
- polycarbonates are produced in a known manner from diphenols, carbonic acid derivatives, optionally chain terminators and optionally branching agents.
- Diphenols suitable for the preparation of the polycarbonates are, for example, hydroquinone, resorcinol, dihydroxydiphenyls, bis (hydroxyphenyl) alkanes, bis (hydroxyphenyl) cycloalkanes, bis (hydroxyphenyl) sulfides, bis (hydroxyphenyl) ethers, Bis (hydroxyphenyl) ketones, bis (hydroxyphenyl) sulfones, bis (hydroxyphenyl) sulfoxides, ⁇ , ⁇ ′-bis (hydroxyphenyl) diisopropylbenzenes, and also their ring-alkylated and ring-halogenated compounds.
- Preferred diphenols are 4,4'-dihydroxydiphenyl, 2,2-bis (4-hydroxyphenyl) propane, 2,4-bis (4-hydroxyphenyl) -2-methylbutane, 1,1-bis (4-hydroxyphenyl ) -p-diisopropylbenzene, 2,2-bis (3-methyl-4-hydroxyphenyl) propane, 2,2-bis (3-chloro-4-hydroxyphenyl) propane, bis (3,5 -dimethyl-4-hydroxyphenyl) methane, 2,2-bis (3,5-dimethyl-4-hydroxyphenyl) propane, bis (3,5-dimethyl-4-hydroxyphenyl) sulfone, 2, 4- bis- (3,5-dimethyl-4-hydroxyphenyl) -2-methylbutane, 1,1-bis (3,5-dimethyl-4-hydroxyphenyl) -p-diisopropylbenzene, 2,2-bis- (3,5-dichloro-4-hydroxyphenyl) propane, 2,2-bis (3,5
- diphenols are 2,2-bis (4-hydroxyphenyl) propane, 2,2-bis (3,5-dimethyl-4-hydroxyphenyl) propane, 2,2-bis (3,5-dichloro) -4-hydroxyphenyl) propane, 2,2-bis (3,5-dibromo-4-hydroxyphenyl) propane, 1,1-bis (4-hydroxyphenyl) cyclohexane and 1,1-bis (4th -hydroxyphenyl) -3, 3,5-trimethylcyclohexane.
- Suitable carbonic acid derivatives are, for example, phosgene or diphenyl carbonate.
- Suitable chain terminators are both monophenols and monocarboxylic acids.
- Suitable monophenols are phenol itself, alkylphenols such as cresols, p-tert-
- the preferred chain terminator is p-tert-butylphenol.
- Suitable monocarboxylic acids are benzoic acid, alkylbenzoic acids and halogenated benzoic acids.
- Preferred chain terminators are the phenols of the formula (I)
- R is hydrogen, tert-butyl or a branched or unbranched C 8 - and / or
- the amount of chain terminator to be used is 0.1 mol% to 5 mol%, based on moles of diphenols used in each case.
- the chain terminators can be added before, during or after phosgenation.
- Suitable branching agents are the tri- or more than triftintional compounds known in polycarbonate chemistry, in particular those with three or more than three phenolic OH groups.
- Suitable branching agents are, for example, phloroglucin, 4,6-dimethyl-2,4,6-tri- (4-hydroxyphenyl) -hepten-2, 4,6-dimethyl-2,4,6-tri- (4-hydroxyphenyl) - heptane, 1, 3,5-tri- (4-hydroxyphenyl) benzene, 1,1,1-tri- (4-hydroxyphenyl) ethane, tri- (4-hydroxyphenyl) phenylmethane, 2,2-bis - [4,4-bis (4-hydroxyphenyl) cyclohexyl] propane, 2,4-bis (4-hydroxyphenyl-isopropyl) phenol, 2,6-bis (2-hydroxy-5'-methyl) -benzyl) -4-methyl- phenol, 2- (4-hydroxyphenyl) -2- (2,4-dihydroxyphenyl) propane, hexa- (4- (4-hydroxyphenylisopropyl) phenyl) orthoterephthalic acid este
- the amount of branching agents which may be used is 0.05 mol% to 2 mol%, based in turn on moles of diphenols used in each case.
- the branching agents can either be introduced with the diphenols and the chain terminators in the aqueous alkaline phase, or added dissolved in an organic solvent before the phosgenation. In the case of the transesterification process, the branching agents are used together with the diphenols.
- thermoplastic polycarbonates All of these measures for the production of the thermoplastic polycarbonates are
- thermoplastics preferably poly- and copolycarbonates
- additional additive usually present in thermoplastics, preferably poly- and copolycarbonates, such as e.g. Flame retardants, fillers, foaming agents, dyes, pigments, optical brighteners, transesterification catalysts and nucleating agents or the like, preferably in amounts of up to 5% by weight, preferably 0.01 to 5% by weight, based on the mixture as a whole, particularly preferably 0 , 01 wt .-% to 1 wt .-% based on the amount of plastic is included.
- additional additive usually present in thermoplastics, preferably poly- and copolycarbonates, such as e.g. Flame retardants, fillers, foaming agents, dyes, pigments, optical brighteners, transesterification catalysts and nucleating agents or the like, preferably in amounts of up to 5% by weight, preferably 0.01 to 5% by weight, based on the mixture as a whole, particularly preferably 0 , 01 wt
- the polymer compositions obtained in this way can be converted into shaped objects, for example toy parts, but also fibers, foils, tapes, plates, multi-wall sheets, vessels, tubes and other profiles by the customary methods, such as hot pressing, spinning, extrusion or injection molding .
- the polymer compositions can also be processed into cast films.
- the invention therefore continues to apply the use of the polymer compositions according to the invention for the production of a shaped article.
- the use of multilayer systems is also of interest.
- the polymer composition according to the invention is applied in a thin layer to a shaped object made of a conventional polymer.
- the application can take place simultaneously or immediately afterwards with the shaping of the base body, e.g. by coextrusion or multi-component injection molding.
- the application can also be done on the finished molded body, e.g. by lamination with a film or by coating with a solution.
- the polycarbonate molding compositions according to the invention can be processed into moldings by, for example, extruding the polycarbonates isolated in a known manner to give granules, and these granules, if appropriate after addition of the additives mentioned above, by injection molding to various articles in a known manner
- the moldings made from the polycarbonate molding compositions according to the invention can be used within a broad spectrum, particularly where dust accumulation is undesirable for the reasons mentioned.
- the application is particularly suitable for optical data carriers, e.g. CDs, automotive components, e.g. Glazing elements, plastic lenses, also for use with extruded sheets, e.g. Solid sheets, double-wall sheets or multi-wall sheets, optionally also with one or more coextruded layers, as well as the use in injection molded parts, such as food containers, components of electrical appliances, in
- polycarbonate molding compositions according to the invention can also be used with conventional others
- Transparent plastics are particularly suitable.
- Transparent thermoplastics are preferred as transparent plastics used, particularly preferably the polymers of ethylenically unsaturated monomers and / or polycondensates of bi-functional reactive compounds.
- plastics for these mixtures are poly- or copolyacrylates and poly- or copolymethacrylates such as poly- or copolymethyl methacrylate, but also particularly copolymers with styrene such as transparent polystyrene-acrylonitrile (SAN), furthermore transparent cycloolefins, poly- or copolycondden- sate of terephthalic acid, such as poly- or copolyethylene terephthalate (PET or CoPET) or glycol-modified PET (PETG).
- SAN transparent polystyrene-acrylonitrile
- SAN transparent polystyrene-acrylonitrile
- poly- or copolycondden- sate of terephthalic acid such as poly- or copolyethylene terephthalate (PET or CoPET) or glycol-modified PET (PETG).
- the sprayed plates are exposed to an atmosphere with whirled up dust.
- a 2-1 beaker with an 80 mm long magnetic stirring bar with a triangular cross section is filled with the respective dust approx. 1 cm high.
- the dust is whirled up with the help of a magnetic stirrer. After stopping the stirrer, the
- Table 2 The dust figures in Table 2 are assessed by the eye. Panels that have delicate dust figures or high contrasts are rated negative (-), those with uniform and large-scale dust figures are rated (+). Table 1:
- Tables 1-3 clearly show that moldings from the molding compositions according to the invention attract less dust, have better transmission after dusting and form optically more beautiful and larger-area dust figures than from conventional molding compositions.
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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)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
- Polyesters Or Polycarbonates (AREA)
- Containers Having Bodies Formed In One Piece (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP00935079A EP1187879A1 (fr) | 1999-06-01 | 2000-05-19 | Matieres a mouler en polycarbonate servant a la realisation de produits attirant peu la poussiere |
CA002374444A CA2374444A1 (fr) | 1999-06-01 | 2000-05-19 | Matieres a mouler en polycarbonate servant a la realisation de produits attirant peu la poussiere |
AU50692/00A AU5069200A (en) | 1999-06-01 | 2000-05-19 | Polycarbonate molding compounds for producing articles with reduced dust attraction |
IL14617300A IL146173A0 (en) | 1999-06-01 | 2000-05-19 | Policarbonate molding compounds for producing articles with reduced dust attraction |
MXPA01012383A MXPA01012383A (es) | 1999-06-01 | 2000-05-19 | Masas de moldeo de policarbonato para la fabricacion de articulos con fijacion de polvo disminuido. |
BR0011245-3A BR0011245A (pt) | 1999-06-01 | 2000-05-19 | Massas de moldar de policarbonato para produção de artigos com acumulação de pó reduzida |
JP2001500707A JP2003501508A (ja) | 1999-06-01 | 2000-05-19 | ダスト吸引性の低い物品を製造するためのポリカーボネート成形用組成物 |
KR1020017015411A KR20020008205A (ko) | 1999-06-01 | 2000-05-19 | 먼지 유인력이 감소된 물품 제조용 폴리카르보네이트 성형배합물 |
HK02108585.2A HK1046921A1 (zh) | 1999-06-01 | 2002-11-28 | 用於生產表現降低的灰塵吸收量製品的聚碳酸酯模塑組合物 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19925125.8 | 1999-06-01 | ||
DE19925125A DE19925125A1 (de) | 1999-06-01 | 1999-06-01 | Polycarbonatformmassen zur Herstellung von Artikeln mit verminderter Staubanlagerung |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000073386A1 true WO2000073386A1 (fr) | 2000-12-07 |
Family
ID=7909910
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2000/004573 WO2000073386A1 (fr) | 1999-06-01 | 2000-05-19 | Matieres a mouler en polycarbonate servant a la realisation de produits attirant peu la poussiere |
Country Status (12)
Country | Link |
---|---|
EP (1) | EP1187879A1 (fr) |
JP (1) | JP2003501508A (fr) |
KR (1) | KR20020008205A (fr) |
CN (1) | CN1353742A (fr) |
AU (1) | AU5069200A (fr) |
BR (1) | BR0011245A (fr) |
CA (1) | CA2374444A1 (fr) |
DE (1) | DE19925125A1 (fr) |
HK (1) | HK1046921A1 (fr) |
IL (1) | IL146173A0 (fr) |
MX (1) | MXPA01012383A (fr) |
WO (1) | WO2000073386A1 (fr) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001090244A1 (fr) * | 2000-05-19 | 2001-11-29 | Dow Global Technologies Inc. | Compositions à base de polymère de carbonate contenant des composés à absorbance uv peu volatils |
DE102009043513A1 (de) | 2009-09-30 | 2011-03-31 | Bayer Materialscience Ag | Polycarbonatzusammensetzungen mit verbesserten optischen Eigenschaften |
US9243125B2 (en) | 2012-09-28 | 2016-01-26 | Sabic Global Technologies B.V. | Release polycarbonate compositions |
US9390744B2 (en) | 2012-09-28 | 2016-07-12 | Sabic Global Technologies B.V. | Polycarbonate composition to produce optical quality products with high quality and good processability |
US9644075B2 (en) | 2013-06-21 | 2017-05-09 | Sabic Global Technologies B.V. | Polycarbonate composition to produce optical quality products with high quality and good processability |
US10150855B2 (en) | 2014-03-06 | 2018-12-11 | Sabic Global Technologies B.V. | Enhanced polycarbonate extrusion grades |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10114803A1 (de) * | 2001-03-26 | 2002-10-10 | Bayer Ag | Neue Polymergemische |
JP5055294B2 (ja) | 2006-12-06 | 2012-10-24 | 帝人化成株式会社 | 眼鏡レンズ |
DE102009043511A1 (de) * | 2009-09-30 | 2011-03-31 | Bayer Materialscience Ag | UV-stabile Polycarbonat-Zusammensetzung mit verbesserten Eigenschaften |
DE102009043512A1 (de) * | 2009-09-30 | 2011-03-31 | Bayer Materialscience Ag | Polycarbonat-Zusammensetzung mit verbesserter Schmelzefließfähigkeit |
EP2374829A1 (fr) * | 2010-04-07 | 2011-10-12 | Bayer MaterialScience AG | Polycarbonate en fusion ramifié doté d'un taux moindre de structures erronées |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0213413A1 (fr) * | 1985-08-02 | 1987-03-11 | Teijin Chemicals, Ltd. | Composition de polycarbonate et son emploi dans des applications optiques |
JPH01284549A (ja) * | 1988-05-12 | 1989-11-15 | Mitsubishi Gas Chem Co Inc | 光学用成形材料 |
JPH02196852A (ja) * | 1989-01-25 | 1990-08-03 | Idemitsu Petrochem Co Ltd | 帯電防止性ポリカーボネート組成物 |
JPH02251560A (ja) * | 1989-03-24 | 1990-10-09 | Idemitsu Petrochem Co Ltd | 眼鏡用樹脂組成物 |
EP0561629A2 (fr) * | 1992-03-17 | 1993-09-22 | Ge Plastics Japan Limited | Compositions de résine de polycarbonate |
JPH0733969A (ja) * | 1993-07-22 | 1995-02-03 | Mitsubishi Gas Chem Co Inc | 耐候性ポリカーボネート樹脂成形品 |
JPH07126505A (ja) * | 1993-11-04 | 1995-05-16 | Mitsubishi Gas Chem Co Inc | 光記録媒体用成形材料 |
US5717021A (en) * | 1996-11-18 | 1998-02-10 | General Electric Company | Polycarbonate/ABS blends |
JPH10168296A (ja) * | 1996-12-13 | 1998-06-23 | Sumitomo Dow Ltd | 滞留熱安定性に優れるポリカーボネート樹脂組成物 |
WO1999005205A1 (fr) * | 1997-07-25 | 1999-02-04 | Bayer Aktiengesellschaft | Matieres de moulage en polycarbonate et leur utilisation comme revetements dans des plaques coextrudees |
EP0979843A2 (fr) * | 1998-08-13 | 2000-02-16 | Idemitsu Petrochemical Co., Ltd. | Composition de résine thermoplastique et des pièces moulées par injection |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW222292B (fr) * | 1991-02-21 | 1994-04-11 | Ciba Geigy Ag | |
US5510450A (en) * | 1992-02-21 | 1996-04-23 | General Electric Company | Method of producing copolymerized polycarbonates |
US5278279A (en) * | 1992-03-11 | 1994-01-11 | Daicel Chemical Industries, Ltd. | Process for producing (co)polycarbonate with transesterification catalyst and compound |
DE4445786A1 (de) * | 1994-12-21 | 1996-06-27 | Bayer Ag | Arylphosphin-haltige Polycarbonate |
DE59702969D1 (de) * | 1996-10-30 | 2001-03-08 | Ciba Sc Holding Ag | Stabilisatorkombination für das Rotomolding-Verfahren |
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1999
- 1999-06-01 DE DE19925125A patent/DE19925125A1/de not_active Ceased
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2000
- 2000-05-19 CN CN00808412A patent/CN1353742A/zh active Pending
- 2000-05-19 IL IL14617300A patent/IL146173A0/xx unknown
- 2000-05-19 KR KR1020017015411A patent/KR20020008205A/ko not_active Application Discontinuation
- 2000-05-19 EP EP00935079A patent/EP1187879A1/fr not_active Withdrawn
- 2000-05-19 CA CA002374444A patent/CA2374444A1/fr not_active Abandoned
- 2000-05-19 BR BR0011245-3A patent/BR0011245A/pt not_active Application Discontinuation
- 2000-05-19 WO PCT/EP2000/004573 patent/WO2000073386A1/fr not_active Application Discontinuation
- 2000-05-19 MX MXPA01012383A patent/MXPA01012383A/es unknown
- 2000-05-19 JP JP2001500707A patent/JP2003501508A/ja active Pending
- 2000-05-19 AU AU50692/00A patent/AU5069200A/en not_active Abandoned
-
2002
- 2002-11-28 HK HK02108585.2A patent/HK1046921A1/zh unknown
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0213413A1 (fr) * | 1985-08-02 | 1987-03-11 | Teijin Chemicals, Ltd. | Composition de polycarbonate et son emploi dans des applications optiques |
JPH01284549A (ja) * | 1988-05-12 | 1989-11-15 | Mitsubishi Gas Chem Co Inc | 光学用成形材料 |
JPH02196852A (ja) * | 1989-01-25 | 1990-08-03 | Idemitsu Petrochem Co Ltd | 帯電防止性ポリカーボネート組成物 |
JPH02251560A (ja) * | 1989-03-24 | 1990-10-09 | Idemitsu Petrochem Co Ltd | 眼鏡用樹脂組成物 |
EP0561629A2 (fr) * | 1992-03-17 | 1993-09-22 | Ge Plastics Japan Limited | Compositions de résine de polycarbonate |
JPH0733969A (ja) * | 1993-07-22 | 1995-02-03 | Mitsubishi Gas Chem Co Inc | 耐候性ポリカーボネート樹脂成形品 |
JPH07126505A (ja) * | 1993-11-04 | 1995-05-16 | Mitsubishi Gas Chem Co Inc | 光記録媒体用成形材料 |
US5717021A (en) * | 1996-11-18 | 1998-02-10 | General Electric Company | Polycarbonate/ABS blends |
JPH10168296A (ja) * | 1996-12-13 | 1998-06-23 | Sumitomo Dow Ltd | 滞留熱安定性に優れるポリカーボネート樹脂組成物 |
WO1999005205A1 (fr) * | 1997-07-25 | 1999-02-04 | Bayer Aktiengesellschaft | Matieres de moulage en polycarbonate et leur utilisation comme revetements dans des plaques coextrudees |
EP0979843A2 (fr) * | 1998-08-13 | 2000-02-16 | Idemitsu Petrochemical Co., Ltd. | Composition de résine thermoplastique et des pièces moulées par injection |
Non-Patent Citations (6)
Title |
---|
DATABASE CHEMABS [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; XP002145510, retrieved from STN Database accession no. 123:171420 * |
DATABASE CHEMABS [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; XP002145511, retrieved from STN Database accession no. 129:136898 * |
DATABASE CHEMABS [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; XP002145512, retrieved from STN Database accession no. 112:181039 * |
DATABASE CHEMABS [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; XP002145513, retrieved from STN Database accession no. 113:213399 * |
DATABASE CHEMABS [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; XP002145514, retrieved from STN Database accession no. 123:288381 * |
DATABASE WPI Section Ch Week 199046, Derwent World Patents Index; Class A23, AN 1990-346127, XP002145515 * |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001090244A1 (fr) * | 2000-05-19 | 2001-11-29 | Dow Global Technologies Inc. | Compositions à base de polymère de carbonate contenant des composés à absorbance uv peu volatils |
DE102009043513A1 (de) | 2009-09-30 | 2011-03-31 | Bayer Materialscience Ag | Polycarbonatzusammensetzungen mit verbesserten optischen Eigenschaften |
US8664349B2 (en) | 2009-09-30 | 2014-03-04 | Bayer Materialscience Ag | Polycarbonate compositions having improved optical properties |
US9243125B2 (en) | 2012-09-28 | 2016-01-26 | Sabic Global Technologies B.V. | Release polycarbonate compositions |
US9390744B2 (en) | 2012-09-28 | 2016-07-12 | Sabic Global Technologies B.V. | Polycarbonate composition to produce optical quality products with high quality and good processability |
US9644075B2 (en) | 2013-06-21 | 2017-05-09 | Sabic Global Technologies B.V. | Polycarbonate composition to produce optical quality products with high quality and good processability |
US10465061B2 (en) | 2013-06-21 | 2019-11-05 | Sabic Global Technologies B.V. | Polycarbonate composition to produce optical quality products with high quality and good processability |
US10150855B2 (en) | 2014-03-06 | 2018-12-11 | Sabic Global Technologies B.V. | Enhanced polycarbonate extrusion grades |
Also Published As
Publication number | Publication date |
---|---|
BR0011245A (pt) | 2002-03-05 |
KR20020008205A (ko) | 2002-01-29 |
DE19925125A1 (de) | 2000-12-07 |
AU5069200A (en) | 2000-12-18 |
HK1046921A1 (zh) | 2003-01-30 |
EP1187879A1 (fr) | 2002-03-20 |
CA2374444A1 (fr) | 2000-12-07 |
CN1353742A (zh) | 2002-06-12 |
JP2003501508A (ja) | 2003-01-14 |
IL146173A0 (en) | 2002-07-25 |
MXPA01012383A (es) | 2002-09-02 |
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