WO2000073377A1 - Matieres a mouler en polycarbonate, a demoulage facile, et corps moules et demi-produits fabriques a partir de ces matieres et presentant de bonnes caracteristiques de glissement - Google Patents

Matieres a mouler en polycarbonate, a demoulage facile, et corps moules et demi-produits fabriques a partir de ces matieres et presentant de bonnes caracteristiques de glissement Download PDF

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Publication number
WO2000073377A1
WO2000073377A1 PCT/EP2000/004677 EP0004677W WO0073377A1 WO 2000073377 A1 WO2000073377 A1 WO 2000073377A1 EP 0004677 W EP0004677 W EP 0004677W WO 0073377 A1 WO0073377 A1 WO 0073377A1
Authority
WO
WIPO (PCT)
Prior art keywords
molding compositions
polycarbonate
compositions according
molded parts
polycarbonate molding
Prior art date
Application number
PCT/EP2000/004677
Other languages
German (de)
English (en)
Inventor
Klaus Horn
Ralf Hufen
Wolfgang Ebert
Klaus Berg
Original Assignee
Bayer Aktiengesellschaft
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 Aktiengesellschaft filed Critical Bayer Aktiengesellschaft
Priority to EP00936785A priority Critical patent/EP1189982A1/fr
Priority to MXPA01012389A priority patent/MXPA01012389A/es
Priority to CA002374445A priority patent/CA2374445A1/fr
Priority to BR0011096-5A priority patent/BR0011096A/pt
Priority to AU52156/00A priority patent/AU5215600A/en
Priority to IL14625600A priority patent/IL146256A0/xx
Priority to JP2001500701A priority patent/JP2003501506A/ja
Priority to KR1020017015409A priority patent/KR20020005766A/ko
Publication of WO2000073377A1 publication Critical patent/WO2000073377A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/10—Esters; Ether-esters
    • C08K5/101—Esters; Ether-esters of monocarboxylic acids
    • C08K5/103—Esters; Ether-esters of monocarboxylic acids with polyalcohols

Definitions

  • Thermoplastics in general and in particular describing polycarbonate are known.
  • the most common substances used as mold release agents are the esters from long-chain aliphatic acids and alcohols. Examples include the use of esters from fatty acid alcohols or polyols such as e.g. Pentaerythritol with fatty acids, as described in DE 33 12 158, EP 100 918, EP 103 107, EP 561 629,
  • fatty acid esters only show a significant release effect from amounts of more than 0.5% by weight.
  • these concentrations often lead to turbidity and or to the formation of mold deposits.
  • Siloxanes which are also used have sufficient temperature resistance, but are very poorly compatible with polycarbonate and, in the concentrations required for effectiveness, lead to undesirable cloudiness which compromises the applicability of severely restrict mainly in transparent settings of common material such as polycarbonate.
  • the task was therefore to find mold release agents that equally minimize both mold release forces in order to enable all mold geometries to be removed from the mold without the formation of mold deposits.
  • Another object is to reduce problems caused by the adhesion of molded polycarbonate moldings, as occurs, for example, when cups are pulled apart after storage.
  • Another object is to reduce problems caused by the adhesion of molded polycarbonate moldings to metals, such as occurs when sliding on inclined metallic planes.
  • Another task is to control the tying force, which e.g. is important for toys.
  • care must be taken to ensure that the components are precisely matched, since insufficient tying force is also undesirable in some applications.
  • the present invention relates to polycarbonate molding compositions with a content of 0.005 to 5.0% by weight, preferably 0.05 to 3.0% by weight, very particularly preferably 0.15 to 2.0% by weight, of fatty acid esters Basis of 1, 2-dihydroxy propane and C ⁇ to C 40 acids and esters of 1,2-dihydroxypropane with mixtures of different Ci to C 4 o-carboxylic acids where the alcohol can also be partially esterified and mixtures of partially esterified and fully esterified products and optionally using other additives customary in polycarbonate, such as, for example, thermal stabilizers, UV stabilizers, other mold release agents,
  • Flame retardants, anti-dripping agents, fillers, glass fibers and blend partners such as ABS, ASA, SAN, EPDM or polyesters based on terephthalic acid and diols, which are characterized in that the molding compositions on a demoulding force measuring tool (friction coefficient measuring tool) for the static and sliding friction coefficients of friction preferably ⁇ 0.80, particularly preferably ⁇ 0.60 and very particularly preferably ⁇ 0.40, the Reference value of a mold release agent-free polycarbonate of the same viscosity measured on the friction coefficient tool has a value between 0.85 and 1.50.
  • demoulding force measuring tool for the static and sliding friction coefficients of friction preferably ⁇ 0.80, particularly preferably ⁇ 0.60 and very particularly preferably ⁇ 0.40
  • the Reference value of a mold release agent-free polycarbonate of the same viscosity measured on the friction coefficient tool has a value between 0.85 and 1.50.
  • the molding compositions according to the invention can be contaminated with impurities which contain the individual constituents of the molding composition from their synthesis, processing, processing and storage, as well as contaminations which originate during the production or processing of the molding compositions according to the invention.
  • the goal is to work with as clean products as possible.
  • the molding compositions if they contain free OH groups, contain less than 10 ppm ions, particularly preferably less than 5 ppm. This is especially true for ions of the elements Na, K, Mg, Ca, Sn, Ti, Fe, Ni, Cr.
  • the fatty acid esters to be used according to the invention if they are partially esterified and contain free OH groups, contain less than 10 ppm ions, particularly preferably less than 5 ppm. This is especially true for ions of the elements Na, K, Mg, Ca, Sn, Ti, Fe, Ni, Cr.
  • the adhesion of molded parts made of polycarbonate is preferably reduced by the content of 1.5% by weight to 2.5% by weight of mold release agent.
  • the fatty acid esters according to the invention are commercially available.
  • 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.
  • Some, up to 80 mol%, preferably from 20 mol% to 50 mol%, of the carbonate groups in the polycarbonates suitable according to the invention can be replaced by aromatic dicarboxylic acid ester groups.
  • aromatic dicarboxylic acid ester groups Such polycarbonates, the Both acidic residues of carbonic acid and acidic residues of aromatic dicarboxylic acids, incorporated into the molecular chain, are, to be precise, aromatic polyester carbonates. For the sake of simplicity, they should be summed up in the present application under the generic term of thermoplastic, aromatic polycarbonates.
  • Preferred diphenols are 4,4'-dihydroxydiphenyl, 2,2-bis (4-hydroxyphenyl) -l-phenyl-propane, l, l-bis- (4-hydroxyphenyl) -phenyl-ethane, 2,2-bis- (4-hydroxyphenyl) propane, 2,4-bis (4-hydroxyphenyl) -2-methylbutane, 1,1-bis (4-hydroxyphenyl) -m / p diisopropylbenzene, 2,2-bis- (3-methyl-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) -m / p
  • diphenols are 4,4'-dihydroxydiphenyl, l, l-bis (4-hydroxyphenyl) phenylethane, 2,2-bis (4-hydroxyphenyl) propane, 2,2-bis (3rd , 5-dimethyl-4-hydroxyphenyl) propane, l, l-bis (4-hydroxyphenyl) cyclohexane and l, l-bis (4-hydroxyphenyl) -3,3,5-trimethylcyclohexane.
  • Suitable chain terminators are both monophenols and monocarboxylic acids.
  • Suitable monophenols are phenol, alkylphenols such as cresols, p-tert-butylphenol, pn-octylphenol, p-iso-octylphenol, pn-nonylphenol and p-iso-nonylphenol, halophenols such as p-chlorophenol, 2,4-dichlorophenol, p-bromophenol and 2,4,6-tribromophenol, or mixtures thereof.
  • Suitable monocarboxylic acids are benzoic acid, alkylbenzoic acids and halogenated benzoic acids.
  • Preferred chain terminators are the phenols of the formula (I)
  • the amount of chain terminator to be used is 0.5 mol% to 10 mol%, based on moles of diphenols used in each case.
  • the chain terminators can be added before, during or after the phosgenation.
  • Suitable branching agents are the trifunctional or trifunctional compounds known in polycarbonate chemistry, in particular those having three or more than three phenolic OH groups.
  • Suitable branching agents are, for example, phloroglucin, 4,6-dimethyl-2,4,6-tri- (4-hydroxyphenyl) -heptene 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-methylphenol, 2- (4-hydroxyphenyl) -2- (2,4-dihydroxyphenyl) propane, hexa- (4- (4-hydroxyphenyl-isopropyl) phenyl) orthoterephthalic acid
  • 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.
  • Aromatic dicarboxylic acids suitable for the production of the polyester carbonates are, for example, phthalic acid, terephthalic acid, isophthalic acid, tert-butylisophthalic acid, 3,3'-diphenyldicarboxylic acid, 4,4'-diphenyldicarboxylic acid, 4,4-benzophenone dicarboxylic acid, 3,4'- Benzophenone dicarboxylic acid, 4,4'-diphenyl ether dicarboxylic acid, 4,4'-diphenyl sulfone dicarboxylic acid, 2,2-bis (4-carboxyphenyl) propane, trimethyl-3-phenyl indane-4,5'-dicarboxylic acid.
  • aromatic dicarboxylic acids terephthalic acid and or isophthalic acid are particularly preferably used.
  • dicarboxylic acids are the dicarboxylic acid dihalides and the dicarboxylic acid dialkyl esters, in particular the dicarboxylic acid dichlorides and the dicarboxylic acid dimethyl esters.
  • the carbonate groups are replaced by the aromatic dicarboxylic acid ester groups essentially stoichiometrically and also quantitatively, so that the molar
  • the ratio of the reactants is also found in the finished polyester carbonate.
  • the aromatic dicarboxylic acid ester groups can be incorporated either statistically or in blocks.
  • Preferred methods of production of the polycarbonates to be used according to the invention, including the polyester carbonates, are the known interfacial process and the known melt transesterification process.
  • phosgene is preferably used as the carbonic acid derivative, in the latter case preferably diphenyl carbonate.
  • Catalysts, solvents, work-up, reaction conditions etc. for the production of polycarbonate are sufficiently described and known in both cases.
  • the molding compositions according to the invention are prepared by adding the alkanes according to the invention into the melt during synthesis or, in the case of the phase interface process, a work-up or concentration step, but also in solution, by simultaneously dissolving the polycarbonates in a polycarbonate solvent or successively mixed with the alkanes according to the invention and optionally further additives and the polycarbonate solvent is then evaporated.
  • the present invention thus also relates to a process for the preparation of the polycarbonate molding compositions according to the invention, which is characterized in that polycarbonates are mixed with the esters according to the invention either simultaneously or successively, either in bulk or in solution, and then the mixtures either at temperatures between 260 ° C and 450 ° C ° C, preferably
  • the polycarbonate molding compositions according to the invention can still be the usual
  • Suitable glass fibers are all commercially available glass fiber types and types, i.e. cut glass types long glass fibers (chopped strands) and short glass (milled fibers), provided that they are compatible with polycarbonate by suitable sizes.
  • Flame retardants such as find use in polycarbonate and can also be used in the molding compositions according to the invention are alkali metal salts of organic and inorganic acids, in particular sulfonic acids such as, for example
  • Injection molding is preferred.
  • the invention therefore also relates to parts made from the molding compositions according to the invention, such as molded parts and semi-finished products.
  • a process data acquisition system measures the breakaway torque of the plate and the pressing force of the tool stamp on the plate. The coefficients are determined from the measurement parameters.
  • the amounts in the examples relate to the weight of the total mixture.
  • the coefficients of friction were measured using a specially made measuring tool.
  • the same plate-shaped molded part was always injected at a melt temperature of 300 ° C at a mold temperature of 90 ° C. After cooling for 20 seconds, the molded part is rotated through an angle of 90 ° in the closed mold.
  • a process data acquisition system measures the breakaway torque of the plate and the pressing force of the tool stamp on the plate. The coefficients are determined from the measurement parameters.
  • Examples 1 and 2 and comparative examples 1 to 3 are listed in Table 1.
  • a mold-free polycarbonate and a product containing PETS pentaerythritol tetrastearate were given as a comparison.
  • the molding compositions according to the invention are distinguished by significantly smaller coefficients of friction and are already more effective in smaller quantities than the standard demoulder PETS used.
  • the molding compositions according to the invention also show low haze and better transmission (examples 3 and 4) at higher mold release contents than comparative example 4 (see table 2).

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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)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Sewing Machines And Sewing (AREA)
  • Noodles (AREA)
  • Purses, Travelling Bags, Baskets, Or Suitcases (AREA)

Abstract

La présente invention concerne des matières à mouler en polycarbonate, à démoulage facile, et des corps moulés et demi-produits fabriqués à partir de ces matières et présentant de bonnes caractéristiques de glissement.
PCT/EP2000/004677 1999-06-01 2000-05-23 Matieres a mouler en polycarbonate, a demoulage facile, et corps moules et demi-produits fabriques a partir de ces matieres et presentant de bonnes caracteristiques de glissement WO2000073377A1 (fr)

Priority Applications (8)

Application Number Priority Date Filing Date Title
EP00936785A EP1189982A1 (fr) 1999-06-01 2000-05-23 Matieres a mouler en polycarbonate, a demoulage facile, et corps moules et demi-produits fabriques a partir de ces matieres et presentant de bonnes caracteristiques de glissement
MXPA01012389A MXPA01012389A (es) 1999-06-01 2000-05-23 Masas de moldeo de policarbonato con buen desmoldeo y cuerpos moldeados fabricados a partir de las mismas y productos semielaborados con buenas propiedades de deslizamiento.
CA002374445A CA2374445A1 (fr) 1999-06-01 2000-05-23 Matieres a mouler en polycarbonate, a demoulage facile, et corps moules et demi-produits fabriques a partir de ces matieres et presentant de bonnes caracteristiques de glissement
BR0011096-5A BR0011096A (pt) 1999-06-01 2000-05-23 Massas de moldar de policarbonato,com boa desmoldação, e corpos moldados e produtos semi-acabados produzidos das mesmas, com boas propriedades de deslizamento
AU52156/00A AU5215600A (en) 1999-06-01 2000-05-23 Polycarbonate moulding materials with good demoulding properties and moulded bodies and semi-finished products produced with said materials, with good sliding properties
IL14625600A IL146256A0 (en) 1999-06-01 2000-05-23 Polycarbonate moulding materials with good demoulding properties and moulded bodies and semi-finished products produced with said materials, with good sliding properties
JP2001500701A JP2003501506A (ja) 1999-06-01 2000-05-23 良好な離型性を有するポリカーボネート成形用組成物、およびこれから製造される成形品および半完成品
KR1020017015409A KR20020005766A (ko) 1999-06-01 2000-05-23 이형 특성이 양호한 폴리카보네이트 성형 재료 및 이를사용하여 제조된, 미끄러짐 특성이 양호한 성형체 및반마감품

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19925116 1999-06-01
DE19925116.9 1999-06-01

Publications (1)

Publication Number Publication Date
WO2000073377A1 true WO2000073377A1 (fr) 2000-12-07

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PCT/EP2000/004677 WO2000073377A1 (fr) 1999-06-01 2000-05-23 Matieres a mouler en polycarbonate, a demoulage facile, et corps moules et demi-produits fabriques a partir de ces matieres et presentant de bonnes caracteristiques de glissement

Country Status (11)

Country Link
EP (1) EP1189982A1 (fr)
JP (1) JP2003501506A (fr)
KR (1) KR20020005766A (fr)
CN (1) CN1353737A (fr)
AR (1) AR024160A1 (fr)
AU (1) AU5215600A (fr)
BR (1) BR0011096A (fr)
CA (1) CA2374445A1 (fr)
IL (1) IL146256A0 (fr)
MX (1) MXPA01012389A (fr)
WO (1) WO2000073377A1 (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090043053A1 (en) * 2007-08-07 2009-02-12 Rudiger Gorny Aircraft window
JP5273877B2 (ja) * 2008-05-28 2013-08-28 帝人株式会社 眼鏡レンズ
WO2011078265A1 (fr) * 2009-12-24 2011-06-30 三菱レイヨン株式会社 Procédé d'évaluation des performances d'un agent organique de démoulage, processus de production d'un moule et processus de production d'un film transparent présentant une structure finement rugosifiée à sa surface
CN103351596A (zh) * 2013-08-08 2013-10-16 深圳市兴盛迪新材料有限公司 一种改进的玻纤增强pc/asa组合物
JP6340238B2 (ja) * 2014-04-17 2018-06-06 住化ポリカーボネート株式会社 遊技機用可動演出役物
JP7253334B2 (ja) * 2018-07-03 2023-04-06 出光興産株式会社 ポリカーボネート系樹脂組成物及びその成形体

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1489717A (en) * 1975-05-07 1977-10-26 Sapchim Fournier Cimag Sa Synthetic plastics materials containing lubricating agent
WO1998017725A1 (fr) * 1996-10-21 1998-04-30 Eastman Chemical Company Melanges polyester a base de 1,4-cyclohexanedimethanol

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1489717A (en) * 1975-05-07 1977-10-26 Sapchim Fournier Cimag Sa Synthetic plastics materials containing lubricating agent
WO1998017725A1 (fr) * 1996-10-21 1998-04-30 Eastman Chemical Company Melanges polyester a base de 1,4-cyclohexanedimethanol

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Publication number Publication date
IL146256A0 (en) 2002-07-25
AR024160A1 (es) 2002-09-04
CA2374445A1 (fr) 2000-12-07
EP1189982A1 (fr) 2002-03-27
JP2003501506A (ja) 2003-01-14
AU5215600A (en) 2000-12-18
KR20020005766A (ko) 2002-01-17
CN1353737A (zh) 2002-06-12
BR0011096A (pt) 2002-06-11
MXPA01012389A (es) 2002-09-02

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