WO2000037562A1 - Verwendung von jod- und/oder bromhaltigen polycarbonaten für formteile mit hohem röntgenkontrast sowie damit hergestellte formteile - Google Patents
Verwendung von jod- und/oder bromhaltigen polycarbonaten für formteile mit hohem röntgenkontrast sowie damit hergestellte formteile Download PDFInfo
- Publication number
- WO2000037562A1 WO2000037562A1 PCT/EP1999/009556 EP9909556W WO0037562A1 WO 2000037562 A1 WO2000037562 A1 WO 2000037562A1 EP 9909556 W EP9909556 W EP 9909556W WO 0037562 A1 WO0037562 A1 WO 0037562A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- weight
- iodine
- brominated
- polycarbonates
- ray contrast
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/04—Aromatic polycarbonates
- C08G64/06—Aromatic polycarbonates not containing aliphatic unsaturation
- C08G64/08—Aromatic polycarbonates not containing aliphatic unsaturation containing atoms other than carbon, hydrogen or oxygen
- C08G64/10—Aromatic polycarbonates not containing aliphatic unsaturation containing atoms other than carbon, hydrogen or oxygen containing halogens
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/39—Markers, e.g. radio-opaque or breast lesions markers
-
- A—HUMAN NECESSITIES
- A63—SPORTS; GAMES; AMUSEMENTS
- A63H—TOYS, e.g. TOPS, DOLLS, HOOPS OR BUILDING BLOCKS
- A63H33/00—Other toys
- A63H33/001—Toy-moulding appliances; Toy moulding
Definitions
- the invention relates to the use of iodine and / or bromine-containing thermoplastics for molded parts with high X-ray contrast and those produced therewith
- Molded parts especially toys and medical devices.
- Such molding materials can be made radiopaque by suitable additives.
- X-ray detectable plastic molding compositions have also been described in Silberman-Hazony, Encycl. Polym. Be. Closely. (1988), 14, 1-8. Thermoplastics with various heavy metals have been described as X-ray contrast media. A halogen-containing terpolymer was also mentioned.
- FR 2223403 describes PVC and other vinyl polymers with iodine-containing salicylic acids, benzoic acids and their esters, which are similar to those of US Pat. Nos. 3,361,700 and 3,645,955.
- PVC is not suitable for applications where high transparency and good mechanical properties are required.
- transparent plastic molding compositions made of polycarbonates with iodine-containing end groups have also been described. In this way, iodine is only introduced at the end groups. All other monomers remain unmodified, which is why the weight fraction of iodine remains limited.
- the layer thickness at which the plastic can still be recognized should be as small as possible, but at most 1.2 mm.
- the task was to develop molding compounds with good mechanics and
- Transparency have sufficient contrast in X-ray examinations.
- the addition of heavy metals should be avoided for toxicological reasons, since materials for children's toys were sought.
- the subject of the present application is accordingly the use of iodine and / or bromine-containing transparent thermoplastics for molded parts with high X-ray contrast.
- Polymers of ethylenically unsaturated monomers and / or polycondensates of bifunctional reactive compounds which contain bromine or iodine are suitable.
- Particularly suitable plastics are polycarbonates or copolycarbonates based on diphenols.
- oligomers according to the invention can, however, also be used with poly- or copolyacrylates and poly- or copolymer-methacrylates such as, for example, brominated and / or iodinated poly- or copolymethyl methacrylate, but also as copolymers with styrene, such as transparent brominated and / or iodinated polyurethane-acrylonitrile
- SAN can be used.
- poly- or copolycondensates of terephthalic acid e.g. Poly- or copolyethylene terephthalate (PET or CoPET) or glycol-modified PET (PETG) can be mixed in.
- PET or CoPET Poly- or copolyethylene terephthalate
- PETG glycol-modified PET
- Brominated and / or iodinated polycarbonates are particularly preferred for moldings with high X-ray contrast, the polycarbonates having an iodine and / or brominated diol unit and a weight average molecular weight Mw
- polycarbonates which, as a diol unit, between 0.1 and 100% by weight, preferably between 1 and 100% by weight, particularly preferably between 10 and 100% by weight, preferably 100% by weight, of brominated and / or iodinated 2,2-bis - (4-hydroxyphenyl) propane included.
- diols are 2,2-bis
- the molded parts can consist entirely of the iodine and / or bromine-containing polycarbonate.
- the iodine and / or bromine content in the molded part is then between 0.2 to
- the moldings then contain the iodine and / or bromine-containing polycarbonates in amounts between 0.1 to 100% by weight, preferably 1 to 30% by weight, particularly preferably 2 to 20% by weight and very particularly preferably 2 to 10 % By weight based on the molded part.
- the molded parts can optionally additionally contain at least one transparent thermoplastic, preferably a non-halogenated polycarbonate or copolycarbonate in amounts of 70 to 99% by weight, preferably 80 to 98% by weight, particularly preferably 90 to 98% by weight, based on the molded part his.
- at least one transparent thermoplastic preferably a non-halogenated polycarbonate or copolycarbonate in amounts of 70 to 99% by weight, preferably 80 to 98% by weight, particularly preferably 90 to 98% by weight, based on the molded part his.
- the polymers of ethylenically unsaturated monomers and / or polycondensates of bifunctional reactive compounds are particularly preferably used as transparent thermoplastics.
- Particularly suitable transparent thermoplastics are polycarbonates or copolycarbonates based on diphenols.
- the oligomers according to the invention can also be mixed with poly- or copolyacrylates and poly- or copolymethacrylates such as e.g. Poly- or copolymethyl methacrylate, but also as copolymers with styrene such as transparent polystyrene acrylonitrile (SAN) can be used.
- SAN transparent polystyrene acrylonitrile
- PET or CoPET poly or copolyethylene terephthalate
- PETG 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.
- 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, ä, ä'-bis- (hydroxyphenyl) diisopropylbenzenes, and their alkylated compounds.
- the iodinated and / or brominated derivatives of these diols are suitable for the preparation of the polycarbonates and / or copolycarbonates according to the invention.
- Preferred for the polycarbonates and / or copolycarbonates according to the invention are tetrabromobisphenol and / or tetraiodobisphenol, optionally in a mixture with one another or optionally with other diols.
- a preferred copolymer for the polycarbonates and / or copolycarbonates according to the invention is one of tetrabromobisphenol with bisphenol A as a comonomer.
- a preferred mixture for the polycarbonates and / or copolycarbonates according to the invention is a mixture of polymers from tetrabromobisphenol with polymers with bisphenol A.
- Preferred diphenols for the additional polycarbonates and / or copolycarbonates 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,
- Particularly preferred diphenols for the additional polycarbonates and or copolycarbonates 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-hj-hydroxyphenyl) propane, 1,1-bis (4-hydroxyphenyl ) -cyclohexane and l, l-bis- (4-hydroxyphenyl) -3,3,5-trimethylcyclohexane.
- Suitable carbonic acid derivatives are, for example, phosgene or diphenyl carbonate.
- Suitable chain terminators for the iodine and / or bromine-containing polycarbonates according to the invention, but also the additional polycarbonates and / or copolycarbonates are both monophenols and monocarboxylic acids.
- Suitable monophenols are phenol itself, alkylphenols such as cresols, p-tert-butylphenol, p-n-octylphenol, p-iso-
- halophenols such as p-chlorophenol, 2,4-dichlorophenol, p-bromophenol and 2,4,6-tribromophenol, especially 2,4,6-triiodophenol, p- Jodpbenol, as well as their mixtures.
- 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 C 9 alkyl radical.
- 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 trifunctional 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, l, 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-hydroxyphenylisopropyl) phenyl) -orthotere
- the amount of the branching agents to be used is from 0.05 mol% to
- 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 producing the thermoplastic polycarbonates are familiar to the person skilled in the art.
- the additional polycarbonates and / or copolycarbonates can be present in amounts between 0 and 99.9% by weight, preferably 70 and 99% by weight, particularly preferably between 80 and 98% by weight and very particularly preferably between 90 and 98% by weight. -% based on the molded part.
- thermoplastics preferably poly- and copolycarbonates, such as e.g. Stabilizers (as described, for example, in EP 0 839 623 AI or EP 0 500 496 AI), in particular thermal stabilizers, in particular organic phosphites or phosphines, mold release agents, for example fatty acid esters of glycerol or tetramethanol methane, where unsaturated fatty acid can also be completely or partially epoxidized, in particular Glycerol monostearate or pentaerytetratetearate (PETS), flame retardants, antistatic agents, UV absorbers, for example triazoles, fillers, foaming agents, dyes, pigments, optical brighteners, and nucleating agents or the like, preferably in amounts of up to 5% by weight, preferably 0.01 up to 5% by weight based on the entire mixture, particularly preferably 0.01% by weight to 1% by weight based on the
- transesterification catalysts known from the literature such as organic tin or titanium compounds, can also optionally be used in the amounts known from the literature, preferably between 10 and
- UV stabilizers from the triazole series.
- the x-ray-opaque polymer compositions thus obtained can be prepared by the usual methods, e.g. Hot pressing, spinning, extruding or injection molding, can be converted into shaped objects, e.g. Toy parts, but also fibers,
- the polymer compositions can also be processed into cast films.
- the invention therefore further relates to 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 invention is also of interest.
- Polymer composition with a relatively high content of bromine- or iodine-containing additives in a thin layer applied to a molded article made of a polymer which is transparent to X-rays The application can take place at the same time or immediately afterwards with the shaping of the base body, for example by coextrusion or multi-component injection molding. However, it can also be applied to the finished molded body, for example by lamination with a film or by coating with a solution.
- the molding compounds are particularly suitable for transparent children's toy parts or for medical applications. Such molded parts are particularly suitable for small parts of children's toys. Examples:
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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)
- Toys (AREA)
- Materials For Medical Uses (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Polyesters Or Polycarbonates (AREA)
- Laminated Bodies (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002355142A CA2355142A1 (en) | 1998-12-18 | 1999-12-07 | Use of polycarbonates containing iodine and/or bromine for moulded parts with high x-ray contrast and moulded parts produced with same |
AU19713/00A AU1971300A (en) | 1998-12-18 | 1999-12-07 | Use of polycarbonates containing iodine and/or bromine for moulded parts with high x-ray contrast and moulded parts produced with same |
EP99963402A EP1141129A1 (de) | 1998-12-18 | 1999-12-07 | Verwendung von jod- und/oder bromhaltigen polycarbonaten für formteile mit hohem röntgenkontrast sowie damit hergestellte formteile |
JP2000589625A JP2002533515A (ja) | 1998-12-18 | 1999-12-07 | ヨウ素及び/または臭素を含むポリカーボネートの、高x線コントラストを示す成形部品への使用法、並びにそれから製造される成形部品 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19858788 | 1998-12-18 | ||
DE19858788.0 | 1998-12-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000037562A1 true WO2000037562A1 (de) | 2000-06-29 |
Family
ID=7891783
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1999/009556 WO2000037562A1 (de) | 1998-12-18 | 1999-12-07 | Verwendung von jod- und/oder bromhaltigen polycarbonaten für formteile mit hohem röntgenkontrast sowie damit hergestellte formteile |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP1141129A1 (de) |
JP (1) | JP2002533515A (de) |
CN (1) | CN1330688A (de) |
AU (1) | AU1971300A (de) |
CA (1) | CA2355142A1 (de) |
WO (1) | WO2000037562A1 (de) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005325319A (ja) * | 2004-04-15 | 2005-11-24 | Teijin Chem Ltd | ポリカーボネート樹脂組成物 |
AU2005272944B2 (en) * | 2004-08-13 | 2009-01-15 | Reva Medical, Inc. | Inherently radiopaque bioresorbable polymers for multiple uses |
JP5347244B2 (ja) * | 2006-08-04 | 2013-11-20 | 三菱化学株式会社 | ハロゲン含有ポリカーボネート樹脂の製造方法 |
EP3237487B1 (de) * | 2014-12-23 | 2021-02-17 | Rutgers, the State University of New Jersey | Biokompatible iodierte diphenolmonomere und polymere |
EA202191884A1 (ru) | 2019-02-28 | 2021-12-08 | Спид Кеа Минерал Гмбх | Паста для маркировки текстильных тканей и/или других продуктов, не способных к рентгеновскому контрасту |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4182787A (en) * | 1978-06-19 | 1980-01-08 | General Electric Company | Optically transparent, radiographically opaque tubing |
EP0359366A2 (de) * | 1988-09-06 | 1990-03-21 | Mitsubishi Kasei Corporation | Medizinische Formkörper und Verfahren zu ihrer Herstellung |
JPH0641416A (ja) * | 1992-07-24 | 1994-02-15 | Nippon Steel Chem Co Ltd | 難燃性ポリカーボネート樹脂組成物およびその成形品 |
EP0585778A2 (de) * | 1992-09-04 | 1994-03-09 | Bayer Ag | Verfahren zur Herstellung von Pulvermischungen für matte Polycarbonat-Formmassen |
JPH0857033A (ja) * | 1994-08-25 | 1996-03-05 | Terumo Corp | X線造影性医療用成型品 |
DE19726191A1 (de) * | 1997-06-20 | 1998-12-24 | Bayer Ag | Verwendung von Jod-phenyl-carbonat-haltigen Polycarbonaten zur Herstellung von speziellen Formteilen |
-
1999
- 1999-12-07 EP EP99963402A patent/EP1141129A1/de not_active Withdrawn
- 1999-12-07 AU AU19713/00A patent/AU1971300A/en not_active Abandoned
- 1999-12-07 JP JP2000589625A patent/JP2002533515A/ja active Pending
- 1999-12-07 WO PCT/EP1999/009556 patent/WO2000037562A1/de not_active Application Discontinuation
- 1999-12-07 CN CN99814500A patent/CN1330688A/zh active Pending
- 1999-12-07 CA CA002355142A patent/CA2355142A1/en not_active Abandoned
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4182787A (en) * | 1978-06-19 | 1980-01-08 | General Electric Company | Optically transparent, radiographically opaque tubing |
EP0359366A2 (de) * | 1988-09-06 | 1990-03-21 | Mitsubishi Kasei Corporation | Medizinische Formkörper und Verfahren zu ihrer Herstellung |
JPH0641416A (ja) * | 1992-07-24 | 1994-02-15 | Nippon Steel Chem Co Ltd | 難燃性ポリカーボネート樹脂組成物およびその成形品 |
EP0585778A2 (de) * | 1992-09-04 | 1994-03-09 | Bayer Ag | Verfahren zur Herstellung von Pulvermischungen für matte Polycarbonat-Formmassen |
JPH0857033A (ja) * | 1994-08-25 | 1996-03-05 | Terumo Corp | X線造影性医療用成型品 |
DE19726191A1 (de) * | 1997-06-20 | 1998-12-24 | Bayer Ag | Verwendung von Jod-phenyl-carbonat-haltigen Polycarbonaten zur Herstellung von speziellen Formteilen |
Non-Patent Citations (2)
Title |
---|
DATABASE WPI Section Ch Week 199411, Derwent World Patents Index; Class A23, AN 1994-089472, XP002135107 * |
DATABASE WPI Section Ch Week 199619, Derwent World Patents Index; Class A96, AN 1996-182599, XP002135042 * |
Also Published As
Publication number | Publication date |
---|---|
CN1330688A (zh) | 2002-01-09 |
AU1971300A (en) | 2000-07-12 |
EP1141129A1 (de) | 2001-10-10 |
CA2355142A1 (en) | 2000-06-29 |
JP2002533515A (ja) | 2002-10-08 |
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