ES2641302T3 - Aplicación superficial de polímeros para mejorar la resistencia del papel - Google Patents

Aplicación superficial de polímeros para mejorar la resistencia del papel Download PDF

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ES2641302T3
ES2641302T3 ES11782337.7T ES11782337T ES2641302T3 ES 2641302 T3 ES2641302 T3 ES 2641302T3 ES 11782337 T ES11782337 T ES 11782337T ES 2641302 T3 ES2641302 T3 ES 2641302T3
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meth
acrylamide
acrylate
component
starch
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Sachin Borkar
Marc C. Putnam
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Solenis Technologies Cayman LP
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Solenis Technologies Cayman LP
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    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H19/00Coated paper; Coating material
    • D21H19/10Coatings without pigments
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/24Homopolymers or copolymers of amides or imides
    • C08L33/26Homopolymers or copolymers of acrylamide or methacrylamide
    • 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
    • C09D103/00Coating compositions based on starch, amylose or amylopectin or on their derivatives or degradation products
    • 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
    • C09D133/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/24Homopolymers or copolymers of amides or imides
    • C09D133/26Homopolymers or copolymers of acrylamide or methacrylamide
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • D21H21/18Reinforcing agents
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/52Amides or imides
    • C08F220/54Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/52Amides or imides
    • C08F220/54Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
    • C08F220/56Acrylamide; Methacrylamide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F226/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
    • C08F226/02Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a single or double bond to nitrogen
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/64Paper recycling

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Paper (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Composición de recubrimiento que comprende el componente a) copolímero catiónico que comprende de 0,01 a 100 por ciento molar de monómero catiónico, en la que dicho copolímero catiónico se prepara a partir de un monómero seleccionado del grupo que consiste en (met)acrilato de dimetilaminoetilo, (met)acrilato de dietilaminoetilo, (met)acrilato de dimetilaminopropilo, (met)acrilato de dietilaminopropilo, (met)acrilamida de N,N-dimetilaminopropilo, cloruro de acrilamidapropiltrimetilamonio, cloruro de trimetilamoniopropilmetacrilamida, dialquilalilamina, dialilamina y alilamina, y un comonómero seleccionado del grupo que consiste en acrilamida, metacrilamida, (met)acrilamida de N-metilo, (met)acrilamida de N-etilo, (met)acrilamida de N,N-dimetilo, (met)acrilamida de N-isopropilo, ácido acrílico, N-vinilformamida, N-vinilacetamida y vinil-N-ftalimida, el componente b) almidón, o bien nativo o bien derivatizado, y opcionalmente, el componente c) un producto químico modificador de la viscosidad; en la que la composición carece de precipitados, coagulados y geles.

Description

imagen1
imagen2
imagen3
imagen4
imagen5
imagen6
*: Comparativo, no según invención
Ejemplo 4 – Comparativo -No según invención
5 Se preparó una mezcla de poliacrilamida catiónica y polivinilamina o polivinilamina modificada (aditivos de rendimiento del papel Hercobond® 6000, disponibles de Ashland Incorporated) mezclando las dos disoluciones de polímero. En un experimento típico, se cargó un tarro de 4 oz con 100 g disolución de poliacrilamida catiónica (PAM) tal como se prepara siguiendo el protocolo del ejemplo 1, a esta se le añadió este producto Hercobond® 6000 al 5%
10 en peso (base sólida total). Se agitó la mezcla de polímeros en un agitador Lab Line® Orbit Environ durante 1 hora a 25ºC.
TABLA 4: Mezcla de poliacrilamida catiónica con polivinilamina
Ejemplos
Denominación PAM Polivinilamina
4-1
Ejemplo 1-4 Hercobond® 6350 al 2,5% en peso
4-2
Ejemplo 1-4 Hercobond® 6350 al 5,0% en peso
15 Ejemplo 5
Usando el método de aplicación al papel anteriormente descrito, se evaluaron las poliacrilamidas catiónicas para determinar el efecto sobre la resistencia de la hoja. Todas las series, excepto la 5-1, contenían el 3% en peso de
20 ExcelSize 15 en la disolución de la prensa encoladora. Los copolímeros que contienen o bien dialilamina o bien dimetilaminopropilmetacrilamida proporcionan resistencia mejorada cuando se aplican a la superficie de hojas de soporte del cartón de cobertura reciclado. Las concentraciones de los aditivos indicados a continuación son en base seca del papel (Aditivo seco sobre peso seco del papel, “d/d”).
25 TABLA 5: Efecto de aditivos a base de acrilamida sobre la resistencia en seco del cartón de cobertura reciclado. La hoja de soporte fabricada usando cartulina ondulada vieja china, peso base = 100 g/m2, espesor 7,4 mil, ExcelSize 15 = almidón de tapioca oxidado
Ejemplos
Aditivo % de aditivo (d/d) Datos de resistencia
Mullen (lb/in2)
RCT (lbf/6 in.)
5-1
Sin almidón - 19,0 21,3
5-2
Sólo almidón - 24,2 29,1
5-3
2-2 0,50 28,2 30,3
5-4
2-2 1,00 33,0 35,5
5-5
1-1 0,50 26,6 28,6
5-6
1-1 1,00 32,0 36,4
5-7
1-3 0,30 27,6 34,7
30 Ejemplo 6
Usando el método de aplicación al papel anteriormente descrito, se evaluaron las poliacrilamidas catiónicas para determinar el efecto sobre la resistencia de la hoja. Todas las series, excepto la 6-1, contenían el 2% en peso de ExcelSize C155 en la disolución de la prensa encoladora. Los copolímeros que contienen metacrilato de N,N
35 dimetilaminoetilo demuestran algo menos de mejora de la resistencia eficaz en comparación con copolímeros que contienen o bien dialilamina o bien dimetilaminopropilmetacrilamida. En el caso de poli(acrilamida-covinilformamida), la eficacia mejora cuanto más hidrolizado está el polímero. Las concentraciones de los aditivos indicados a continuación son en base seca del papel. (Aditivo seco sobre peso seco de papel)
40 TABLA 6: Efecto de aditivos a base de acrilamida sobre la resistencia en seco del cartón de cobertura reciclado. La hoja de soporte fabricada usando cartulina ondulada vieja americana, peso base = 198 g/m2, espesor = 11,5 mil, ExcelSize C155 = almidón de tapioca oxidado y ligeramente catiónico.
Ejemplos
Aditivo % de aditivo (d/d) Datos de resistencia
Mullen (lb/in2)
RCT (lbf/6 in.)
6-1
Sin almidón - 58,1 84,4
6-2
Sólo almidón - 69,8 98,7
6-3
1-1 0,5 77,6 105,8
6-4
1-1 1,0 81,6 115,4
6-5
1-5 0,5 68,4 106,9
6-6
1-5 1,0 73,4 109,2
6-7
1-6 0,5 74,6 107,4
6-8
1-6 1,0 74,0 112,6
8
6-9
2-1 0,5 73,6 107,1
6-10
2-1 1,0 80,4 108,6
Comparativo 6-11
3-1 0,5 66,0 98,0
Comparativo 6-12
3-1 1,0 72,4 106,3
6-13
3-2 0,5 71,6 105,9
6-14
3-2 1,0 71,1 109,4
6-15
3-3 0,5 73,7 105,2
6-16
3-3 1,0 76,0 107,9
6-17
3-4 0,5 73,4 109,6
6-18
3-4 1,0 77,9 109,0
Ejemplo 7
Usando el método de aplicación al papel anteriormente descrito, se evaluaron las poliacrilamidas catiónicas para
5 determinar el efecto sobre la resistencia de la hoja usando cartulina ondulada vieja americana, una hoja de soporte fuerte. Todas las series, excepto la 7-1, contenían el 2% en peso de almidón ExcelSize 15 en la disolución de la prensa encoladora. El uso de aditivo catiónico mostró mejora de la resistencia, sin embargo, la mejora de la resistencia global observada es menor en comparación con la observada en cartulina ondulada vieja china. Las concentraciones de los aditivos indicados a continuación son en base seca en el papel.
10 TABLA 7 Efecto de aditivos a base de acrilamida sobre la resistencia en seco del cartón de cobertura reciclado. La hoja de soporte fabricada usando cartulina ondulada vieja americana, peso base = 198 g/m2, espesor = 11,5 mil, ExcelSize 15 = almidón de tapioca oxidado
Ejemplos
Aditivo % de aditivo (d/d) Datos de resistencia
Mullen (lb/in2)
RCT (lbf/6 in.)
7-1
Sin almidón - 58,1 97,8
7-2
Sólo almidón - 76,1 123,3
7-3
2-2 0,5 84,4 119,9
7-4
2-2 1,0 82,4 125,4
7-5
1-6 1,0 76,6 126,8
7-6
1-1 0,25 78,0 131,3
7-7
1-1 0,5 81,8 126,6
9

Claims (1)

  1. imagen1
ES11782337.7T 2010-11-05 2011-10-31 Aplicación superficial de polímeros para mejorar la resistencia del papel Active ES2641302T3 (es)

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US41048310P 2010-11-05 2010-11-05
US410483P 2010-11-05
PCT/US2011/058620 WO2012061305A1 (en) 2010-11-05 2011-10-31 Surface application of polymers to improve paper strength

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EP (1) EP2635645B1 (es)
JP (1) JP5893041B2 (es)
KR (2) KR101836210B1 (es)
CN (1) CN103201348B (es)
AU (1) AU2011323632B2 (es)
CA (1) CA2813996C (es)
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MX (1) MX343488B (es)
PL (1) PL2635645T3 (es)
PT (1) PT2635645T (es)
TW (1) TWI575135B (es)
WO (1) WO2012061305A1 (es)
ZA (1) ZA201304082B (es)

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PL2635645T3 (pl) 2017-11-30
EP2635645A1 (en) 2013-09-11
AU2011323632B2 (en) 2016-03-10
CA2813996C (en) 2015-01-27
MX2013004106A (es) 2013-07-17
TWI575135B (zh) 2017-03-21
KR20180027633A (ko) 2018-03-14
KR20130117804A (ko) 2013-10-28
ZA201304082B (en) 2014-12-23
WO2012061305A1 (en) 2012-05-10
EP2635645B1 (en) 2017-07-05
CA2813996A1 (en) 2012-05-10
KR101836210B1 (ko) 2018-03-09
CN103201348A (zh) 2013-07-10
US8900412B2 (en) 2014-12-02
KR101946221B1 (ko) 2019-02-08
PT2635645T (pt) 2017-08-11
JP2013543066A (ja) 2013-11-28
JP5893041B2 (ja) 2016-03-23
MX343488B (es) 2016-11-08
TW201229358A (en) 2012-07-16
AU2011323632A1 (en) 2013-06-27
US20120111517A1 (en) 2012-05-10
CN103201348B (zh) 2017-02-15

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