ES2599203T3 - Materiales de tinta líquida y películas hechas a partir de los mismos - Google Patents

Materiales de tinta líquida y películas hechas a partir de los mismos Download PDF

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Publication number
ES2599203T3
ES2599203T3 ES12733372.2T ES12733372T ES2599203T3 ES 2599203 T3 ES2599203 T3 ES 2599203T3 ES 12733372 T ES12733372 T ES 12733372T ES 2599203 T3 ES2599203 T3 ES 2599203T3
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grams
films made
liquid ink
film
ink materials
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Susan M. Endle
Corey J. Radloff
Jeffrey J. Schwab
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3M Innovative Properties Co
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3M Innovative Properties Co
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B67/00Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0071Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/02Emulsion paints including aerosols
    • C09D5/024Emulsion paints including aerosols characterised by the additives
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/22Luminous paints
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K9/00Tenebrescent materials, i.e. materials for which the range of wavelengths for energy absorption is changed as a result of excitation by some form of energy
    • C09K9/02Organic tenebrescent materials

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Dispersion Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Paints Or Removers (AREA)
  • Silicon Compounds (AREA)
  • Luminescent Compositions (AREA)
  • Silicon Polymers (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

Un material de teñido líquido filmógeno que comprende: una dispersión acuosa polimérica; un agente de teñido dispersado en la dispersión polimérica acuosa, en donde el agente de teñido está encapsulado en una pluralidad de partículas híbridas orgánicas-inorgánicas; en donde tras entrar en contacto con un sustrato, el material de teñido líquido filmógeno se seca para formar una película que sea transparente y que se pueda teñir.

Description

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DS-10: Dodecilbencenosulfonato de sodio.
HJB: Una pasta acuosa de pigmento de color negro, obtenida con la designación comercial “1-11-JET BLACK30B465” de Penn Color, Inc., Doylestown, Pennsylvania.
M-600: Una polieteramina, obtenida con la designación comercial “JEFFAMINE M-600” de Huntsman Chemical Corporation, The Woodlands, Texas.
NMP: N-Metil-2-pirrolidona.
PPES: Polipropilenoxisilano, preparada de la siguiente forma: Se añadieron 50 gramos de M-600 a un frasco de cristal con una barra agitadora. Se añadieron gota a gota 19:6 gramos de isocianato de trietoxisililpropano a Jeffamine y se agitaron durante 2 horas a 21 °C. El producto de reacción, PPES, se usó sin purificación.
PSSA: Ácido poliestireno sulfonato co málieco).
PTMS: Feniltrimetoxisilano.
RM-8W: Un modificador de la reología no iónico, obtenido con la designación comercial “ACRYSOL RM-8W” de Dow Chemical Company, Midland, Michigan.
RM-12W: Un modificador de la reología no iónico, obtenido con la designación comercial “ACRYSOL RM-12W” de Dow Chemical Company.
RSP: Un tinte fotocrómico, obtenido con la designación comercial “REVERSACOL STORM PURPLE” de Vivimed Labs Ltd., Hyderabad, India.
RU 13-825: Un poliuretano, obtenido con la designación comercial “RU 13-825” de Stahl USA, Inc., Peabody, Massachusetts.
EPCD1: Un tinte fotocrómico encapsulado, preparado de la siguiente forma. A un matraz de fondo redondo de 1000 ml provisto de un agitador se añadieron 437,5 ml de una solución de hidróxido sódico 6 milimolar, 35 gramos de BTC, y la mezcla se agitó a 21 °C hasta que el BTC se disolvió. 35 gramos de una solución de tinte de silano que contenía un 0,33% en peso de RSP, 33% en peso de PTMS, y 66,67% en peso de A1230 se añadió usando una minibomba VWR de flujo variable a un caudal de 0,1 ml/minuto. La agitación continuó durante al menos dos horas tras completar la adición de la solución de tinte-silano. A continuación se añadieron 437,5 ml de acetato de etilo y el contenido se transfirió a un embudo de decantación grande. La capa orgánica, un 8,2% en peso de ECDP1, a continuación se recogió en un matraz de fondo redondo.
EPCD2: Un tinte fotocrómico encapsulado, se preparó como se ha descrito de forma general en ECDP1, en donde el A1230 se sustituyó por un peso igual de PPES.
EPCD3: Un tinte fotocrómico encapsulado, preparado de la siguiente forma. 178 gramos de una solución de hidróxido sódico 30 milimolar se añadieron a un frasco de vidrio de 473 ml (16 oz), seguido por 11 gramos de DS-l0, y la mezcla se agitó a 21 °C hasta que el DS-10 se disolvió. Continuando con la agitación, se añadieron 11 gramos de una solución de silano-tinte al 1% en peso en PTMS usando la minibomba VWR de flujo variable a un caudal de 0,1 ml/minuto. La agitación continuó durante al menos 2 h a 21 °C, tras completar la adición de la solución RSP-PTMS. El tamaño de partículas promedio de las partículas resultantes se determinó en 30,0 nm de diámetro. La distribución de tamaño de partículas se determinó mediante dispersión de luz dinámica (DLS) usando un analizador de tamaño de partículas modelo “ZETASIZER-NANOZSTM” obtenido con Malvern Instruments, Malvern, Reino Unido. Los soles de muestra se prepararon en agua para realizar mediciones de DLS. Una pequeña alícuota (0,1 — 0,5 ml) se extrajo del sol y se diluyó con 2 ml de agua. La muestra diluida resultante se mezcló bien y después se transfirió a una cubeta de plástico. Se registraron los datos de dispersión de luz después de ajustar la temperatura de la muestra a 25 °C. Para transformar la función de autocorrelación en tamaño de partículas, se utilizaron valores normalizados para la viscosidad (0,8872 x 10-3 Pa.s; 0,8 cps) y el índice de refracción (1,33) del agua a 25 °C. Se usó un valor de 1,428 como el índice de refracción de la sílice amorfa. El diámetro promedio en Z notificado (diámetro de partícula promedio, d, en nm) se basó en una distribución ponderada según la intensidad. Todos los resultados se notificaron en términos del tamaño de partículas, d (nm).
Ejemplo 1
103,3 gramos de n-metil-2-pirrolidona (NMP) se combinaron con 393,4 gramos de 8,2% en peso de EPCD1 en acetato de etilo. El acetato de etilo se eliminó de la mezcla con un evaporador rotatorio, dando como resultado 34% en peso de sol de EPCD1 en NMP. Se añadieron a continuación 5 gramos de cada uno de RU 13-825 y EPCD1-NMP y se mezclaron a 2500 revoluciones usando un mezclador por vortización, modelo “MV 1 MINI VORTEXER” obtenido de IKA Works, Inc., Wilmington, Carolina del Norte. Se introdujeron aproximadamente 1-2 gramos de la mezcla en un porta
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Claims (1)

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ES12733372.2T 2011-06-28 2012-06-27 Materiales de tinta líquida y películas hechas a partir de los mismos Active ES2599203T3 (es)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201161501799P 2011-06-28 2011-06-28
US201161501799P 2011-06-28
US13/532,307 US9382428B2 (en) 2011-06-28 2012-06-25 Liquid tint materials and films made therefrom
US201213532307 2012-06-25
PCT/US2012/044303 WO2013003404A1 (en) 2011-06-28 2012-06-27 Liquid tint materials and films made therefrom

Publications (1)

Publication Number Publication Date
ES2599203T3 true ES2599203T3 (es) 2017-01-31

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US (2) US9382428B2 (es)
EP (2) EP2726571B1 (es)
JP (1) JP5963856B2 (es)
CN (2) CN103619990A (es)
BR (1) BR112013033698A2 (es)
CA (1) CA2840605A1 (es)
ES (1) ES2599203T3 (es)
WO (2) WO2013003264A1 (es)

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US20140128608A1 (en) 2014-05-08
WO2013003404A1 (en) 2013-01-03
CN103649241B (zh) 2016-08-17
EP2726563B1 (en) 2016-07-20
US20130001830A1 (en) 2013-01-03
EP2726571B1 (en) 2016-05-25
BR112013033698A2 (pt) 2018-07-03
CA2840605A1 (en) 2013-01-03
EP2726571A4 (en) 2015-02-25
EP2726571A1 (en) 2014-05-07
JP2014527094A (ja) 2014-10-09
US9382428B2 (en) 2016-07-05
EP2726563A1 (en) 2014-05-07
WO2013003264A1 (en) 2013-01-03
CN103649241A (zh) 2014-03-19
JP5963856B2 (ja) 2016-08-03
US9163145B2 (en) 2015-10-20
CN103619990A (zh) 2014-03-05

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