ES2639197T3 - Cuerpo multicapa de policarbonato con efecto de brillo profundo - Google Patents
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- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
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- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
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- B32B27/00—Layered products comprising a layer of synthetic resin
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- C08K5/0041—Optical brightening agents, organic pigments
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- C08K5/0091—Complexes with metal-heteroatom-bonds
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- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C08K5/18—Amines; Quaternary ammonium compounds with aromatically bound amino groups
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- C08K5/00—Use of organic ingredients
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- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
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- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3442—Heterocyclic compounds having nitrogen in the ring having two nitrogen atoms in the ring
- C08K5/3462—Six-membered rings
- C08K5/3465—Six-membered rings condensed with carbocyclic rings
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- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
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- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2255/00—Coating on the layer surface
- B32B2255/10—Coating on the layer surface on synthetic resin layer or on natural or synthetic rubber layer
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/40—Properties of the layers or laminate having particular optical properties
- B32B2307/402—Coloured
- B32B2307/4026—Coloured within the layer by addition of a colorant, e.g. pigments, dyes
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/40—Properties of the layers or laminate having particular optical properties
- B32B2307/406—Bright, glossy, shiny surface
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- B60—VEHICLES IN GENERAL
- B60J—WINDOWS, WINDSCREENS, NON-FIXED ROOFS, DOORS, OR SIMILAR DEVICES FOR VEHICLES; REMOVABLE EXTERNAL PROTECTIVE COVERINGS SPECIALLY ADAPTED FOR VEHICLES
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- C08J2300/00—Characterised by the use of unspecified polymers
- C08J2300/22—Thermoplastic resins
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- C08J2483/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
- C08J2483/04—Polysiloxanes
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24942—Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
- Y10T428/2495—Thickness [relative or absolute]
- Y10T428/24967—Absolute thicknesses specified
- Y10T428/24975—No layer or component greater than 5 mils thick
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
- Y10T428/263—Coating layer not in excess of 5 mils thick or equivalent
- Y10T428/264—Up to 3 mils
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Abstract
Cuerpo multicapa que comprende: 1) una capa de base que contiene * al menos un material termpolástico, * al menos un colorante seleccionado del grupo que consiste en las estructuras 1a, 1b:`**Fórmula** en las que - Ra y Rb independientemente entre sí representan un resto alquilo lineal o ramificado o halógeno; - n representa independientemente del R respectivo un número natural entre 0 y 3, siendo el resto para n >= 0 hidrógeno; y 2a, 2b:**Fórmula** en las que - Rc y Rd independientemente entre sí representan un resto alquilo lineal o ramificado o halógeno; - n representa independientemente del R respectivo un número natural entre 0 y 3, siendo el resto para n >= 0 hidrógeno; con una transmisión de luz de la capa de base inferior al 1 %, determinada según la norma ISO 13468-2, 2) al menos en un lado de la capa de base un recubrimiento resistente al rayado a base de polisiloxano con un grosor de 2 a 15 μm, que contiene al menos un absorbedor UV, n donde, siempre que los colorantes de las estructuras (1a), (1b), (2a) y (2b) se empleen individualmente, estos colorantes se emplean en cada caso en concentraciones del 0,05 al 0,50 % en peso.
Description
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las coordenadas de cromaticidad (CIE) y se calcula según la norma ASTM E313. A este respecto se resta el valor de medición del disolvente de laca puro (diacetona alcohol/ 2-metoxipropanol (15 % % en peso / 85 % en peso) de los valores de medición respectivos, es decir la solución de laca coloreada.
Materiales para la fabricación de las probetas:
- •
- Bisfenol A lineal-policarbonato con grupos terminales a base de fenol con un índice de fluidez volumétrico (MVR) de 6 cm3/10 min, medido a 300 °C y 1,2 kg de carga según la norma ISO 1033), denominado a continuación PC
1.
- •
- Bisfenol A lineal-policarbonato con grupos terminales a base de fenol con un MVR de 12,5 cm3/10 min, medido a 300 °C y 1,2 kg de carga según la norma ISO 1033), denominado a continuación como PC 2. PC 2 contiene aún una mezcla de aditivos que consiste en agente de desmoldeo, termoestabilizador y estabilizador UV. Como agente de desmoldeo se emplea tetraestearato de pentaeritritol (CAS 115-83-3), como termoestabilizador trifenilfosfina (CAS 603-35-0) y como estabilizador UV Tinuvin® 329 (CAS 3147-75-9).
- •
- Como negro de humo nanométrico (tamaño de partícula aproximadamente 17 nm) se emplean Black Pearls® 800 (n.º de CAS 1333-86-4) de la empresa Cabot Corp.
Colorante
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- Como colorante de fórmula (1a, 1b) se usa el producto de I (todas las R = H, véase más adelante).
- •
- Como colorante de fórmula (2a, 2b) se usa el producto de II (todas las R = H, véase más adelante).
- •
- Como colorante de fórmula (3) se usa Macrolex Violet B (Solvent Violet 13, n.º de CAS 81-48-1) de la empresa Lanxess AG, Leverkusen.
I) Preparación de una mezcla 1:1 (% en peso) de (1a) y (1b):
Se disponen 5,62 g (0,025 mol) de dianhídrido de ácido beceno-1,2,4,5-tetracarboxílico y 7,99 g (0,05 mol) de 1,8diaminonaftaleno en 75 ml de n-etilpirrolidona a temperatura ambiente y se calienta lentamente hasta 150 °C. A esta temperatura se agita durante 5 horas. Tras enfriar se añaden 125 ml de agua y se separa por filtración el precipitado formado. El precipitado se suspende aún varias veces en agua y se lava de esta manera. El precipitado se seca a alto vacío a 80°C. El precipitado secado se mezcla con una mezcla de 50 ml de ácido acético y 25 ml de anhídrido acético. La mezcla se hierve durante 4 horas a reflujo. Tras enfriar se añade la mezcla de reacción en 500 ml de agua. El precipitado se separa por filtración, se lava con agua y se seca a alto vacío a 80 °C. Se obtienen 12,5 g de polvo de color lila.
II) Preparación de una mezcla 1:1 (% en peso) de (2a) y (2b):
Se disponen 6,71 g (0,025 mol) de dianhídrido de ácido naftaleno-1,4,5,8-tetracarboxílico y 7,99 g (0,05 mol) de 1,8diaminonaftaleno en 75 ml de n-etilpirrolidona a temperatura ambiente y se calienta lentamente a 150 °C. A esta temperatura se agita durante 5 horas. Tras enfriar se añaden 152 ml de agua y se separa por filtración el precipitado formado. El precipitado se suspende aún varias veces en agua y se lava de esta manera. El precipitado se seca a alto vacío a 80 °C. El precipitado secado se mezcla con una mezcla de 50 ml de ácido acético y 25 ml de anhídrido acético. La mezcla se hierve durante 4 horas a reflujo. Tras enfriar se añade la mezcla de reacción en 125 ml de agua. El precipitado se separa por filtración, se lava con agua caliente y se seca a alto vacío a 80 °C. Se obtienen 13,7 g de polvo de color lila.
Preparación de las composiciones de polímero termoplásticas mediante combinación:
La combinación de los aditivos tuvo lugar en una extrusora de doble árbol de la empresa KraussMaffei Berstorff, TYP ZE25, a una temperatura de carcasa de 260°C o una temperatura de medición de 270°C y una velocidad de giro de 100 rpm con un caudal de 10 kg/h con las cantidades de componentes indicadas en los ejemplos. En este caso se prepara para el mejor mezclado una mezcla de polvo de PC 1 (10 % en peso de mezcla de polvo con respecto a la composición total) que contiene los componentes adicionales indicados a continuación. Esta mezcla de polvo se dosifica a la combinación a PC 2.
Fabricación de las probetas:
El granulado se seca a 120 °C durante 3 horas a vacío y a continuación se procesa en una máquina de moldeo por inyección de tipo Arburg 370 con una unidad de inyección 25 a una temperatura de masa de 300°C y una temperatura de herramienta de 90 °C dando placas redondas ópticas con un diámetro de 80 mm y un grosor de 2,0 mm.
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Ejemplo 1 (Ejemplo comparativo)
Se produce una composición de polímero que contiene las cantidades de los siguientes componentes tal como se describió anteriormente mediante combinación:
Macrolex Violett B (colorante para ejemplo comparativos): 0,20 % en peso Black Pearls® 800 (componente b)): 0,02 % en peso
5 Se preparan como anteriormente placas de muestra y granulado.
Ejemplo 2 (de acuerdo con la invención)
Se prepara una composición de polímero que contiene las cantidades de los siguientes componentes tal como se describió anteriormente mediante combinación:
mezcla 1:1 (% en peso) de (1a) y (1b) (componente a)): 0,10 % en peso mezcla 1:1 (% en peso) de (2a) y (2b) (componente a)): 0,10 % en peso
10 Se preparan como anteriormente placas de muestra y granulado. Medición de la transmisión de luz: Las placas de muestra de los Ejemplos 1 y 2 presentan una transmisión de luz inferior al 0,1 %. Comparación visual: Las placas de muestra de los Ejemplos 1 y 2 se comparan visualmente. Estas presentan una superficie libre de
15 defectos y una impresión de color negro suficiente. Tabla 1: Prueba de sangrado en el granulado (tal como se describió anteriormente)
- Duración de extracción
- YI Ejemplo 1 (comparativo) YI Ejemplo 2
- 0 min
- 0 0
- 30 min
- -6,8 -2,6
- 60 min
- -11,6 -4,5
- 120 min
- -20,4 -7,4
- 180 min
- -29,9 -9,2
- 270 min
- -41,8 -11,7
- 24 h
- -113,3 -28,6
Se aprecia claramente que en el material comparativo, a pesar del uso de negro de humo, la solución de laca se tiñe claramente más que en el caso del granulado de acuerdo con la invención. En el caso de cuerpos moldeados, que
20 presentan una superficie claramente menor que el granulado, con el uso de la composición de acuerdo con la invención no ha de temerse sangrado alguno, mientras que en el caso del material comparativo existe el riesgo de tinción de la solución de laca.
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Claims (1)
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imagen1 imagen2 imagen3 imagen4
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11191314 | 2011-11-30 | ||
| EP11191314 | 2011-11-30 | ||
| PCT/EP2012/073712 WO2013079477A1 (de) | 2011-11-30 | 2012-11-27 | Mehrschichtkörper aus polycarbonat mit tiefenglanzeffekt |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2639197T3 true ES2639197T3 (es) | 2017-10-25 |
Family
ID=47263338
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES12794298.5T Active ES2639197T3 (es) | 2011-11-30 | 2012-11-27 | Cuerpo multicapa de policarbonato con efecto de brillo profundo |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20140322509A1 (es) |
| EP (1) | EP2785795B1 (es) |
| JP (1) | JP6178332B2 (es) |
| KR (1) | KR101992509B1 (es) |
| CN (1) | CN103946310B (es) |
| BR (1) | BR112014012633A2 (es) |
| ES (1) | ES2639197T3 (es) |
| WO (1) | WO2013079477A1 (es) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2935437B1 (de) * | 2012-12-20 | 2025-07-02 | Covestro Deutschland AG | Organische farbmittel und eingefärbte polymer-zusammensetzungen mit guten verarbeitungseigenschaften |
| ITRM20120656A1 (it) * | 2012-12-20 | 2014-06-21 | Bayer Materialscience Ag | Articolo multistrato a base di policarbonato con forte resistenza agli agenti atmosferici. |
| CN108440543A (zh) * | 2017-02-16 | 2018-08-24 | 北京鼎材科技有限公司 | 萘嵌间二氮杂苯衍生物 |
| EP3395875B2 (de) | 2017-04-24 | 2023-01-25 | Covestro Deutschland AG | Laserstrahl-durchlässiges substratmaterial für sensoranwendungen |
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-
2012
- 2012-11-27 EP EP12794298.5A patent/EP2785795B1/de active Active
- 2012-11-27 ES ES12794298.5T patent/ES2639197T3/es active Active
- 2012-11-27 CN CN201280058368.2A patent/CN103946310B/zh active Active
- 2012-11-27 BR BR112014012633A patent/BR112014012633A2/pt not_active Application Discontinuation
- 2012-11-27 KR KR1020147014196A patent/KR101992509B1/ko active Active
- 2012-11-27 US US14/359,317 patent/US20140322509A1/en not_active Abandoned
- 2012-11-27 WO PCT/EP2012/073712 patent/WO2013079477A1/de not_active Ceased
- 2012-11-27 JP JP2014543861A patent/JP6178332B2/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| WO2013079477A1 (de) | 2013-06-06 |
| BR112014012633A2 (pt) | 2017-06-13 |
| EP2785795B1 (de) | 2017-06-07 |
| KR20140105444A (ko) | 2014-09-01 |
| JP6178332B2 (ja) | 2017-08-09 |
| US20140322509A1 (en) | 2014-10-30 |
| CN103946310A (zh) | 2014-07-23 |
| CN103946310B (zh) | 2016-03-02 |
| EP2785795A1 (de) | 2014-10-08 |
| JP2015506854A (ja) | 2015-03-05 |
| KR101992509B1 (ko) | 2019-06-24 |
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