WO2006049546A1 - Composition de pigment sous forme de dispersion aqueuse - Google Patents

Composition de pigment sous forme de dispersion aqueuse Download PDF

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Publication number
WO2006049546A1
WO2006049546A1 PCT/SE2005/001523 SE2005001523W WO2006049546A1 WO 2006049546 A1 WO2006049546 A1 WO 2006049546A1 SE 2005001523 W SE2005001523 W SE 2005001523W WO 2006049546 A1 WO2006049546 A1 WO 2006049546A1
Authority
WO
WIPO (PCT)
Prior art keywords
composition
particles
silica
pigment
paper
Prior art date
Application number
PCT/SE2005/001523
Other languages
English (en)
Inventor
Kjell Rune Andersson
Joakim Carlen
Erik Lindgren
Original Assignee
Akzo Nobel N.V.
Eka Chemicals Ab
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 Akzo Nobel N.V., Eka Chemicals Ab filed Critical Akzo Nobel N.V.
Priority to JP2007540280A priority Critical patent/JP5159312B2/ja
Priority to CA2586205A priority patent/CA2586205C/fr
Priority to BRPI0517258-6A priority patent/BRPI0517258A/pt
Priority to MX2007003617A priority patent/MX2007003617A/es
Priority to NZ554299A priority patent/NZ554299A/en
Priority to EP05793349A priority patent/EP1809711A1/fr
Priority to CN2005800358612A priority patent/CN101426865B/zh
Priority to AU2005301350A priority patent/AU2005301350B2/en
Publication of WO2006049546A1 publication Critical patent/WO2006049546A1/fr
Priority to NO20072903A priority patent/NO20072903L/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING 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
    • C09D17/00—Pigment pastes, e.g. for mixing in paints
    • C09D17/004—Pigment pastes, e.g. for mixing in paints containing an inorganic pigment
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING 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
    • C09D17/00—Pigment pastes, e.g. for mixing in paints
    • 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
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/34—Silicon-containing compounds

Definitions

  • US Patent 4554181 discloses a recording surface including a combination of a water soluble polyvalent metal and a cationic polymer.
  • US Patent Application Publication 2004/0255820 discloses a pigment that is surface treated with a water-soluble polyvalent metal salt.
  • one aspect of the invention concerns a pigment composition in the form of an aqueous dispersion comprising:
  • Colloidal primary particles of silica or aluminosilicate have preferably been formed from an aqueous solution of alkali metal silicate where alkali metal ions are removed through an ion exchange process or where the pH of the alkali metal silicate solution has been reduced by the addition of an acid.
  • a process based on ion exchange follows the basic principles described in R.K. Her, "The Chemistry of Silica” 1979, pages 333-334 and results in an aqueous sol comprising colloidal negatively or positively charged particles of silica or aluminosilicate.
  • a process based on pH-reduction of alkali metal silicate follows the basic principles described in e.g. US patents 5176891 , 5648055, 5853616, 5482693, 6060523 and 6274112.
  • sols comprise colloidal primary particles of silica that may or may not be surface modified, for example with a metal oxide such as oxide of aluminium, titanium, chromium, zirconium, boron or any other suitable metal.
  • a metal oxide such as oxide of aluminium, titanium, chromium, zirconium, boron or any other suitable metal.
  • the surface area of the primary particles is from about 30 m 2 /g to about 600 m 2 /g, more preferably from about 30 to about 450 m 2 /g, most preferably from about 40 m 2 /g to about 400 m 2 /g particularly most preferably from about 50 m 2 /g to about 300 m 2 /g.
  • the dry content of the aqueous sol of primary particles is preferably from about 0.5 wt% to about 60 wt%, most preferably from about 1 wt% to about 50 wt%.
  • Suitable aqueous sols of colloidal primary particles of silica or aluminosilicate are commercially available, for example under the trademarks LudoxTM, SnowtexTM, BindzilTM, NyacolTM, VinnsilTM or FennosilTM.
  • a sol formed by dispersing a powder of e.g. precipitated silica, gel-type silica or fumed silica the colloidal particles in a sol prepared from alkali metal silicate by ion exchange or pH-reduction have never been dried to a powder, such as in the case for e.g. precipitated silica or gel-type silica.
  • Aggregation of primary particles in a sol to form a dispersion of porous aggregates may be performed with any suitable method, such as those described in R. K. Her, "The Chemistry of Silica” 1979, pages 364-407.
  • the degree of aggregation can be followed by measuring the viscosity and applying the Einstein and Mooney equations (see e.g. R.K. Her, "The Chemistry of Silica” 1979, pages 360-364).
  • the aggregation may be performed as a separate step or in a mixture also comprising other pigment particles.
  • a salt preferably selected from divalent, multivalent or complex salts, is added to an anionic or cationic sol also resulting in the formation of porous aggregates.
  • salts are aluminium chloride, poly aluminium chloride, poly aluminium silicate sulfate, aluminium sulfate, zirconium carbonates, zirconium acetates, alkali metal borates, and mixtures thereof.
  • a bridging substance is used to form the aggregates from the primary particles.
  • Each porous aggregate is formed from at least three primary particles, which inherently gives at least some pores.
  • the mean particle diameter of the aggregates is preferably from about 0.03 to about 25 ⁇ m, more preferably from about 0.05 to about 10 ⁇ m, most preferably from about 0.1 ⁇ m to about 5 ⁇ m. It is to be understood that the average diameter of the porous aggregates is always larger than the average diameter of the primary particles they are formed from.
  • the surface area of the aggregates is usually essentially the same as of the primary particles.
  • the pigment particles of synthetic amorphous silica or aluminosilicate is a mixture of colloidal particles in a sol prepared from alkali metal silicate by ion exchange or pH-reduction, optionally partially or fully aggregated, with particles of one or more of precipitated silica, gel-type silica or fumed silica.
  • the water soluble aluminium salt in the pigment composition can be any aluminium containing salt and is preferably present in an amount from about 0.1 wt% to about 30 wt% most preferably from about 0.2 wt% to about 15 wt%, calculated as wt% AI 2 O 3 on dry pigment particles.
  • salts include aluminium chloride, poly aluminium chloride, poly aluminium silicate sulfate, aluminium sulfate, zirconium carbonates, zirconium acetates , and mixtures thereof.
  • the aluminium may be present partly or fully on the surface of the particles of silica or aluminosilicate or in the aqueous phase.
  • the cationic polymer in the pigment composition has a molecular weight from about 2000 to about 1000000, preferably from about 2000 to about 500000, most preferably from about 5000 to about 200000.
  • the charge density is from about 0.2 meq/g to about 12 meq/g, preferably from about 0.3 meq/g to about 10 meq/g, most preferably from about 0.5 meq/g to about 8 meq/g.
  • the cationic polymer is preferably present in the pigment dispersion in an amount from about 0.1 wt% to about 30 wt%, more preferably from about 0.5 wt% to about 20 wt%, most preferably from about 1 wt% to about 15 wt%, based on the amount of dry pigment particles.
  • the composition further comprises other kinds of pigment particles such as kaolinites, smectites, talcites, calcium carbonate minerals, precipitated calcium carbonate, and mixtures thereof.
  • the content of synthetic amorphous silica or aluminosilicate particles is preferable from about 10 to 100 wt%, most preferable from about 30 wt% to 100 wt% of the total amount of pigment particles.
  • the pigment composition may also comprise other additives commonly used for paper coating such as stabilisers, rheology modifiers, optical brighteners, lubricants, insolubilizers, dyes, sizing agents etc, as well as various impurities from the raw materials.
  • the dry content of the pigment composition is preferably from about 2 wt% to about 75 wt%, most preferably from about 10 wt% to about 70 wt%.
  • the total amount of other additives (apart from optional binders) and possible impurities is preferably from 0 to about 50 wt%, most preferably from 0 to about 30 wt%, based on the dry content.
  • the invention further relates to a process for the production of a pigment composition as described above comprising mixing particles of synthetic amorphous silica or aluminosilicate, a water soluble aluminium salt and a cationic polymer having a molecular weight from about 2000 to about 1000000 and a charge density from about 0.2 meq/g to about 12 meq/g to an aqueous dispersion in a way so substantial gelling or precipitation is avoided.
  • This can be achieved by several alternative process embodiments.
  • Another alternative process comprises a step of adding particles of synthetic amorphous silica or aluminosilicate to an aqueous solution of a cationic polymer as described above followed by adding a water soluble aluminium salt.
  • Other components such as other pigment particles or binders may be added at any stage in the form of solids, liquids or dispersions.
  • the silica or aluminium silicate particles may be in the form of a solid powder or an aqueous sol of colloidal particles, that may be anionic or cationic. Unless a cationic sol is used, the cationic polymer is preferably in such an excess that it is sufficient for rendering the resulting dispersion predominantly cationic. At least if an anionic sol is used, there may be at least some aggregation of the colloidal particles.
  • Still another process embodiment comprises a step of mixing a cationic aluminium modified aqueous sol of colloidal silica or aluminosilicate with a cationic polymer.
  • a cationic aluminium modified aqueous sol of colloidal silica or aluminosilicate with a cationic polymer.
  • Other components such as other pigment particles or binders may be added at any stage in the form of solids, liquids or dispersions. Regarding suitable and preferred amounts and kinds of the components, the above description of the pigment composition is referred to.
  • the invention also concerns the use of a pigment composition as described above for coating paper or paper board.
  • the invention further concerns a process for the production of coated paper or paperboard comprising a step of applying a pigment composition as described above as a coating to at least one side of a paper or paperboard web.
  • coating refers to any method in which pigments are applied to the surface of paper or paper board, thus including not only conventional coating but also other methods such as for example pigmenting.
  • the invention finally concerns paper or paper board suitable for ink-jet printing obtainable by a process as described above.
  • Such paper or paper board comprises a substantially transparent or substantially non-transparent layer comprising pigment particles of synthetic amorphous silica or aluminosilicate and optionally other pigment particles from the coating composition, the pigment particles preferably forming a nano- structure.
  • the dry amount of coating is preferably from about 0.5 g/m 2 to about 50 g/m 2 , most preferably from about 1.0 g/m 2 to about 25 g/m 2 .
  • the amount of pigment particles from the above described pigment composition per coated side of the paper or paper board is preferably from about 0.7 g/m 2 to about 40 g/m 2 , most preferably from about 1 g/m 2 to about 20 g/m 2 . Preferably no other kind of coating has been applied on top of this layer.
  • the paper or paper board of the invention have particularly good properties for ink-jet printing, giving low line blurriness and mottling and high printing density for colours, but can advantageously also be used for other kinds of printing processes like toner, flexography, letter press, gravure, offset lithography and screen printing. It is a particular advantage that such good properties can be obtained in a simple manner by applying only small amounts of the coating and without the need to apply numerous different coating layers on the paper or paper board. This also enable the coating to be applied with a size press, such as a film press, which for practical reasons is advantageous. Furthermore, the main components of the pigment composition can be made from readily available raw materials.
  • LocronTM was diluted with 3.5 g water and SylojetTM-PVA slurry was mixed with the
  • the print results were evaluated using a print picture with seven colour blocs: cyan, magenta, yellow, red, green, blue and black.
  • the printed blocs and the unprinted paper were measured with a spectrophotometer (Color Touch 2 from Technidyne) and the colour gamut volume was calculated.
  • the gamut volume is approximated with a dodecahedral in the CEI L*a*b* colour space and the measurements of the colours give the corners in the dodecahedral (see "Rydefalk Staffan, Wedin Michael; Litterature review on the colour Gamut in the Printing Process-Fundamentals, PTF-report no 32, May 1997").
  • the results are shown in the table below:
  • Example 2 In these formulation pigment blends with equal parts (dry/dry) of the gel-type silica used was SylojetTM P612 (same as in Example 1) and an anionic silica sol, NyacolTM 9950 from Eka Chemicals, a 50 wt% sol with a mean particle size of 100 nm. As binder the same amount and the same kind of PVA as in Example 1 was used. Two coating formulations with a total pigment content of 20 wt% were prepared. A) 5 g dry silica gel (SylojetTM P612) was dispersed in solution containing 10 g NyacolTM 9950., 20 g 10 wt% PVA and 15 g water under UltraTurraxTM mixing (lO OOOrpm).
  • Example 3 In the test an anionic silica sol, BindzilTM 50/80 from Eka Chemicals was used as pigment, a 50 wt% sol with a mean particle size of 40 nm. Two formulations were prepared without any PVA-binder. A) BindzilTM 50/80 diluted to 30 wt%. B) 6 g LocronTM was diluted with 20 g water and 60 g of BindzilTM 50/80 was added under vigorous mixing (UltraTurraxTM). The mixing continued during the addition of 3 g polyDADMAC (same as in example 1) and 11 g water. The final concentration of silica became 30 wt%.
  • Example 2 Following the same procedure as in Example 1, the coatings were applied to paper and dried (coat weight 8-9 g/m 2 ) and evaluated on two printers. The results are shown in the table below:

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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)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Polymers & Plastics (AREA)
  • Inorganic Chemistry (AREA)
  • Paper (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)
  • Ink Jet Recording Methods And Recording Media Thereof (AREA)
  • Paints Or Removers (AREA)
  • Ink Jet (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Abstract

L'invention concerne une composition de pigment sous forme de dispersion aqueuse qui comprend: (a) des particules de pigment en silice synthétique amorphe ou aluminosilicate; (b) au moins un sel d'aluminium hydrosoluble; et (c) au moins un polymère cationique de poids moléculaire compris entre environ 2 000 et environ 1 000 000 et de densité de charge comprise entre environ 0,2 et environ 12 meq/g. On décrit aussi un procédé pour la fabrication de cette composition, l'utilisation correspondante de la composition telle que décrite, et enfin un procédé de revêtement de papier ou de carton, et du papier ou du carton ainsi revêtu.
PCT/SE2005/001523 2004-11-08 2005-10-13 Composition de pigment sous forme de dispersion aqueuse WO2006049546A1 (fr)

Priority Applications (9)

Application Number Priority Date Filing Date Title
JP2007540280A JP5159312B2 (ja) 2004-11-08 2005-10-13 水性分散液の形態の顔料組成物
CA2586205A CA2586205C (fr) 2004-11-08 2005-10-13 Composition de pigment sous forme de dispersion aqueuse
BRPI0517258-6A BRPI0517258A (pt) 2004-11-08 2005-10-13 composição de pigmento na forma de dispersão aquosa
MX2007003617A MX2007003617A (es) 2004-11-08 2005-10-13 Composicion de pigmento en la forma de dispersion acuosa.
NZ554299A NZ554299A (en) 2005-10-13 2005-10-13 Pigment composition with silica in the form of aqueous dispersion for coating paper
EP05793349A EP1809711A1 (fr) 2004-11-08 2005-10-13 Composition pigmentaire sous forme de dispersion aqueuse
CN2005800358612A CN101426865B (zh) 2004-11-08 2005-10-13 水分散体系形式的颜料组合物
AU2005301350A AU2005301350B2 (en) 2004-11-08 2005-10-13 Pigment composition in the form of aqueous dispersion
NO20072903A NO20072903L (no) 2004-11-08 2007-06-07 Pigmentsammensetning i formen av vandig dispersjon

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP04105595.5 2004-11-08
EP04105595 2004-11-08

Publications (1)

Publication Number Publication Date
WO2006049546A1 true WO2006049546A1 (fr) 2006-05-11

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Application Number Title Priority Date Filing Date
PCT/SE2005/001523 WO2006049546A1 (fr) 2004-11-08 2005-10-13 Composition de pigment sous forme de dispersion aqueuse
PCT/SE2005/001522 WO2006049545A1 (fr) 2004-11-08 2005-10-13 Composition de pigment sous forme de dispersion aqueuse
PCT/SE2005/001524 WO2006049547A1 (fr) 2004-11-08 2005-10-13 Processus de production de papier couche

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PCT/SE2005/001522 WO2006049545A1 (fr) 2004-11-08 2005-10-13 Composition de pigment sous forme de dispersion aqueuse
PCT/SE2005/001524 WO2006049547A1 (fr) 2004-11-08 2005-10-13 Processus de production de papier couche

Country Status (16)

Country Link
EP (3) EP1809711A1 (fr)
JP (3) JP4897694B2 (fr)
KR (3) KR100887002B1 (fr)
CN (3) CN101056956B (fr)
AR (3) AR051614A1 (fr)
AU (3) AU2005301351B2 (fr)
BR (3) BRPI0517262A (fr)
CA (3) CA2586207C (fr)
MX (3) MX2007003617A (fr)
MY (3) MY145100A (fr)
NO (3) NO20072903L (fr)
NZ (1) NZ554297A (fr)
RU (3) RU2375397C2 (fr)
TW (3) TWI308583B (fr)
WO (3) WO2006049546A1 (fr)
ZA (3) ZA200704417B (fr)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010504445A (ja) * 2006-09-26 2010-02-12 エボニック デグサ コーポレーション 増強させた印刷性能のための多機能紙
JP2010505048A (ja) * 2006-09-27 2010-02-18 チバ ホールディング インコーポレーテッド 珪質組成物および製紙におけるその使用
WO2010149676A1 (fr) 2009-06-26 2010-12-29 Akzo Nobel Chemicals International B.V. Substrat revetu et son procede de preparation
US8114486B2 (en) 2006-02-28 2012-02-14 Evonik Degussa Corporation Colored paper and substrates coated for enhanced printing performance
US8834680B2 (en) 2007-07-16 2014-09-16 Akzo Nobel N.V. Filler composition
US11479917B2 (en) 2014-03-14 2022-10-25 Stora Enso Oyj Method for manufacturing a packaging material and a packaging material made by the method

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8758886B2 (en) 2005-10-14 2014-06-24 International Paper Company Recording sheet with improved image dry time
US7682438B2 (en) 2005-11-01 2010-03-23 International Paper Company Paper substrate having enhanced print density
CA2676855A1 (fr) * 2007-02-06 2008-08-14 Sappi Netherlands Services B.V. Methode de preparation d'enduits et papiers en etant recouverts
AU2008219820B2 (en) * 2007-02-26 2013-01-10 Akzo Nobel N.V. Pigment composition
CA2710804C (fr) 2007-12-26 2013-07-02 International Paper Company Substrat de papier contenant un agent mouillant et presentant une marbrure d'impression amelioree
BRPI0906327B1 (pt) 2008-03-31 2020-10-13 International Paper Company folha de registro e método para fabricar folha de registro
CA2726253C (fr) 2008-05-29 2013-08-27 International Paper Company Papier a jet d'encre rapidement couche a sec
WO2010039996A1 (fr) 2008-10-01 2010-04-08 International Paper Company Substrat de papier contenant un agent mouillant et présentant une imprimabilité améliorée
FR2944034B1 (fr) * 2009-04-01 2011-06-03 Arjo Wiggins Fine Papers Ltd Papier fin mat imprimable et son procede de preparation
WO2011026070A1 (fr) * 2009-08-31 2011-03-03 Newpage Corporation Support d'enregistrement à jet d'encre
US8574690B2 (en) 2009-12-17 2013-11-05 International Paper Company Printable substrates with improved dry time and acceptable print density by using monovalent salts
US8652593B2 (en) 2009-12-17 2014-02-18 International Paper Company Printable substrates with improved brightness from OBAs in presence of multivalent metal salts
US8440053B2 (en) 2010-04-02 2013-05-14 International Paper Company Method and system using surfactants in paper sizing composition to inhibit deposition of multivalent fatty acid salts
US8608908B2 (en) 2010-04-02 2013-12-17 International Paper Company Method and system using low fatty acid starches in paper sizing composition to inhibit deposition of multivalent fatty acid salts
US8586156B2 (en) 2010-05-04 2013-11-19 International Paper Company Coated printable substrates resistant to acidic highlighters and printing solutions
SE536746C2 (sv) * 2010-05-12 2014-07-08 Stora Enso Oyj En komposition innehållande mikrofibrillerad cellulosa och en process för tillverkning av en komposition
AU2011280943B2 (en) 2010-07-23 2013-06-13 International Paper Company Coated printable substrates providing higher print quality and resolution at lower ink usage
JP5575594B2 (ja) * 2010-09-17 2014-08-20 富士フイルム株式会社 インク組成物、インクセットおよび画像形成方法
WO2012067976A1 (fr) 2010-11-16 2012-05-24 International Paper Company Composition d'encollage de papier contenant un sel de calcium (ii) et des produits d'acides organiques, son procédé d'utilisation et procédé de préparation
BR112013010260A2 (pt) 2010-11-17 2020-09-01 Hewlett-Packard Development Company, L.P. composição de colagem superfícial, método para fazer uma composição de colagem superfícial, meio de impressão para impressão digital direta, método de fazer o meio de impressão e sistema de impressão digital
JP5817601B2 (ja) * 2012-03-14 2015-11-18 株式会社リコー トナー、並びに、現像剤及び画像形成装置
EP2733260B1 (fr) * 2012-11-20 2019-02-20 Kemira Oyj Procédé de fabrication d'une composition de revêtement, composition de revêtement et son utilisation
FI126543B (fi) * 2013-05-17 2017-02-15 Fp-Pigments Oy Menetelmä pigmenttejä sisältävän kationisen, korkean kuiva-aineen vesidispersion valmistamiseksi, pigmenttejä käsittävä vesidispersio ja sen käyttö
KR101637934B1 (ko) * 2015-03-30 2016-07-08 한국화학연구원 다공성 알루미노 실리카의 제조방법 및 이에 따라 제조되는 다공성 알루미노 실리카
CN105200849A (zh) * 2015-09-23 2015-12-30 西安石油大学 二氧化硅直接涂覆纸基质的方法
CN107034735A (zh) * 2017-03-30 2017-08-11 天长市天达纸箱纸品厂 一种纸箱包装用高强度耐水再生纸板的制备方法
FI128151B (fi) * 2017-10-11 2019-11-15 Build Care Oy Polymeeridispersio ja menetelmä sen valmistamiseksi
CN108914687A (zh) * 2018-08-08 2018-11-30 岳阳林纸股份有限公司 一种造纸纳米微涂工艺及纳米涂层胶版印刷纸
EP3947814A1 (fr) 2019-04-02 2022-02-09 Kemira OYJ Amélioration de la résistance du papier à l'aide de chélates métalliques et de polymères cationiques synthétiques
US11697727B2 (en) * 2019-12-16 2023-07-11 The Goodyear Tire & Rubber Company Silica coated starch
CN114671700B (zh) * 2022-02-25 2023-04-11 广西福美新材料有限公司 一种带装饰图案的改性无机粉复合饰面片材及其制备方法

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2862668A1 (fr) * 2003-11-24 2005-05-27 Honnorat Rech S & Services Papier non couche apte a une impression jet d'encre de qualite renforcee
EP1580019A1 (fr) * 2004-03-25 2005-09-28 Fuji Photo Film Co., Ltd. Matériau pour l'enregistrement par jet d'encre.

Family Cites Families (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3400834C1 (de) * 1984-01-12 1985-02-28 Kernforschungsanlage Jülich GmbH, 5170 Jülich Messgeraet zur Bestimmung des Profils von Gesteinsbohrloechern
JPS6157379A (ja) * 1984-08-28 1986-03-24 Mitsubishi Paper Mills Ltd インクジエツト記録媒体
DE3707221A1 (de) * 1987-03-06 1988-09-15 Nicolaus Md Papier Kationisch eingestellte pigmentdispersion und streichfarbe
JPH0698824B2 (ja) * 1987-11-30 1994-12-07 本州製紙株式会社 インクジェット記録用紙
US4946557A (en) * 1988-03-08 1990-08-07 Eka Nobel Ab Process for the production of paper
JPH03243668A (ja) * 1990-02-21 1991-10-30 Taoka Chem Co Ltd 塗布組成物
US5169441A (en) * 1990-12-17 1992-12-08 Hercules Incorporated Cationic dispersion and process for cationizing finely divided particulate matter
JPH06183131A (ja) * 1992-12-16 1994-07-05 Mitsubishi Paper Mills Ltd インクジェット記録シート
JPH08118787A (ja) * 1994-10-27 1996-05-14 Canon Inc 記録媒体及び画像形成方法
US5551975A (en) * 1994-06-23 1996-09-03 J. M. Huber Corporation Structured pigment compositions, methods for preparation and use
JP2930287B2 (ja) * 1994-11-08 1999-08-03 日本製紙株式会社 記録用紙及びその製造方法
US6548149B1 (en) * 1996-04-24 2003-04-15 Oji Paper Co., Ltd. Ink jet recording material and process for producing same
JPH1193092A (ja) * 1997-09-11 1999-04-06 Hymo Corp 紙用表面塗布剤
CO5070714A1 (es) 1998-03-06 2001-08-28 Nalco Chemical Co Proceso para la preparacion de silice coloidal estable
JP4237409B2 (ja) * 1998-07-01 2009-03-11 キャボット コーポレイション 被覆用組成物および記録媒体
JP4704564B2 (ja) * 1998-10-02 2011-06-15 キャボット コーポレイション シリカ分散体、コーティング組成物、及び記録媒体
WO2000026306A1 (fr) * 1998-11-03 2000-05-11 Engelhard Corporation Composition et procede de fabrication d'argiles fortement gonflantes
JP2000272224A (ja) * 1999-03-25 2000-10-03 Mitsubishi Paper Mills Ltd インクジェット記録用シート
JP4051838B2 (ja) * 1999-04-26 2008-02-27 王子製紙株式会社 被記録体及びその製造方法
JP4460676B2 (ja) * 1999-05-24 2010-05-12 バンドー化学株式会社 Ｖリブドベルト及びその製造方法
AU4255200A (en) * 1999-08-10 2001-02-15 Felix Schoeller Technical Papers, Inc. High gloss ink-jet recording material
US6391427B1 (en) * 1999-12-02 2002-05-21 Eastman Kodak Company Ink jet recording element
GB9930127D0 (en) * 1999-12-22 2000-02-09 Arjo Wiggins Fine Papers Ltd Ink jet printing paper
AU1006001A (en) * 2000-01-06 2001-07-12 Westvaco Corporation Glossy inkjet coated paper
DE60119799T2 (de) * 2000-01-28 2007-04-26 Oji Paper Co., Ltd. Tintenstrahlaufzeichnungsmaterial
JP2001301311A (ja) * 2000-04-18 2001-10-31 Oji Paper Co Ltd インクジェット記録シート及びその製造方法
US6435659B1 (en) * 2000-06-05 2002-08-20 Hewlett-Packard Company Inkjet inks which improve drop-velocity stability and prolong resistor life in inkjet pens
JP4315581B2 (ja) * 2000-08-08 2009-08-19 日清紡ホールディングス株式会社 インクジェット記録用シート
JP2002145609A (ja) * 2000-11-02 2002-05-22 Oji Paper Co Ltd シリカ微粒子分散液の製造方法
JP2002172850A (ja) * 2000-12-07 2002-06-18 Konica Corp インクジェット記録用紙
JP2002338232A (ja) * 2001-05-18 2002-11-27 Nippon Chem Ind Co Ltd 二次凝集コロイダルシリカとその製造方法及びそれを用いた研磨剤組成物
CN100436707C (zh) * 2001-06-11 2008-11-26 巴斯福股份公司 用于纸张的湿强度整理剂
JP2003072233A (ja) * 2001-06-21 2003-03-12 Tomoegawa Paper Co Ltd インクジェット記録シート
US7056969B2 (en) * 2001-10-09 2006-06-06 Kanzaki Specialty Papers, Inc. Ink jet recording material suitable for use in wide format printing applications
JP3854879B2 (ja) * 2002-03-11 2006-12-06 王子製紙株式会社 カチオン性シリカ微粒子凝集体分散液の製造方法及び記録用シート
JP2004001239A (ja) * 2002-03-26 2004-01-08 Konica Minolta Holdings Inc インクジェット記録用紙
JP2004001240A (ja) * 2002-04-05 2004-01-08 Konica Minolta Holdings Inc インクジェット記録用紙
JP2003312139A (ja) * 2002-04-26 2003-11-06 Mitsubishi Paper Mills Ltd インクジェット記録材料およびインクジェット記録用インク
JP4420609B2 (ja) * 2002-05-31 2010-02-24 三菱製紙株式会社 インクジェット記録材料
US20040033377A1 (en) * 2002-06-10 2004-02-19 Koenig Michael F. Waterfast dye fixative compositions for ink jet recording sheets
JP2004058318A (ja) * 2002-07-25 2004-02-26 Fuji Photo Film Co Ltd インクジェット記録用シート
JP4092160B2 (ja) * 2002-09-03 2008-05-28 北越製紙株式会社 インクジェット記録用光沢紙
DE60320671T2 (de) * 2002-11-12 2009-06-10 Nippon Paper Industries Co. Ltd. Tintenstrahlaufzeichnungsmedium und herstellungsverfahren dafür
JP2005138406A (ja) * 2003-11-06 2005-06-02 Oji Paper Co Ltd インクジェット記録用シート
JP4250121B2 (ja) * 2004-07-02 2009-04-08 富士フイルム株式会社 インクジェット記録用媒体

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2862668A1 (fr) * 2003-11-24 2005-05-27 Honnorat Rech S & Services Papier non couche apte a une impression jet d'encre de qualite renforcee
EP1580019A1 (fr) * 2004-03-25 2005-09-28 Fuji Photo Film Co., Ltd. Matériau pour l'enregistrement par jet d'encre.

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP1809711A1 *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8114486B2 (en) 2006-02-28 2012-02-14 Evonik Degussa Corporation Colored paper and substrates coated for enhanced printing performance
JP2010504445A (ja) * 2006-09-26 2010-02-12 エボニック デグサ コーポレーション 増強させた印刷性能のための多機能紙
JP2012136031A (ja) * 2006-09-26 2012-07-19 Evonik Degussa Corp 増強させた印刷性能のための多機能紙
JP2010505048A (ja) * 2006-09-27 2010-02-18 チバ ホールディング インコーポレーテッド 珪質組成物および製紙におけるその使用
US8834680B2 (en) 2007-07-16 2014-09-16 Akzo Nobel N.V. Filler composition
EP2362016B1 (fr) 2007-07-16 2019-01-30 Akzo Nobel Chemicals International B.V. Composition de remplissage
WO2010149676A1 (fr) 2009-06-26 2010-12-29 Akzo Nobel Chemicals International B.V. Substrat revetu et son procede de preparation
US11479917B2 (en) 2014-03-14 2022-10-25 Stora Enso Oyj Method for manufacturing a packaging material and a packaging material made by the method

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