EP1392920B1 - Nappe fibreuse enduite et procede de production de ladite nappe - Google Patents
Nappe fibreuse enduite et procede de production de ladite nappe Download PDFInfo
- Publication number
- EP1392920B1 EP1392920B1 EP02716870A EP02716870A EP1392920B1 EP 1392920 B1 EP1392920 B1 EP 1392920B1 EP 02716870 A EP02716870 A EP 02716870A EP 02716870 A EP02716870 A EP 02716870A EP 1392920 B1 EP1392920 B1 EP 1392920B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- filler
- fibrous web
- fibrils
- light scattering
- coating
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims description 15
- 238000004519 manufacturing process Methods 0.000 title abstract description 8
- 230000008569 process Effects 0.000 title description 5
- 239000000945 filler Substances 0.000 claims abstract description 58
- 238000000576 coating method Methods 0.000 claims abstract description 51
- 239000011248 coating agent Substances 0.000 claims abstract description 48
- 239000000049 pigment Substances 0.000 claims abstract description 33
- 239000000463 material Substances 0.000 claims abstract description 32
- 239000002245 particle Substances 0.000 claims abstract description 21
- 239000000835 fiber Substances 0.000 claims abstract description 20
- 238000000149 argon plasma sintering Methods 0.000 claims abstract description 16
- 229920002678 cellulose Polymers 0.000 claims abstract description 13
- 239000001913 cellulose Substances 0.000 claims abstract description 13
- 238000007670 refining Methods 0.000 claims abstract description 11
- 239000011247 coating layer Substances 0.000 claims abstract description 5
- 238000012216 screening Methods 0.000 claims abstract 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 44
- 239000000203 mixture Substances 0.000 claims description 24
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 19
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 14
- 239000000454 talc Substances 0.000 claims description 11
- 229910052623 talc Inorganic materials 0.000 claims description 11
- 235000012211 aluminium silicate Nutrition 0.000 claims description 10
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 10
- 239000005995 Aluminium silicate Substances 0.000 claims description 9
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 7
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 6
- 239000001175 calcium sulphate Substances 0.000 claims description 5
- 235000011132 calcium sulphate Nutrition 0.000 claims description 5
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 4
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 4
- 229910021502 aluminium hydroxide Inorganic materials 0.000 claims description 4
- PZZYQPZGQPZBDN-UHFFFAOYSA-N aluminium silicate Chemical compound O=[Al]O[Si](=O)O[Al]=O PZZYQPZGQPZBDN-UHFFFAOYSA-N 0.000 claims description 4
- 229910000323 aluminium silicate Inorganic materials 0.000 claims description 4
- QXDMQSPYEZFLGF-UHFFFAOYSA-L calcium oxalate Chemical compound [Ca+2].[O-]C(=O)C([O-])=O QXDMQSPYEZFLGF-UHFFFAOYSA-L 0.000 claims description 4
- 239000010440 gypsum Substances 0.000 claims description 4
- 229910052602 gypsum Inorganic materials 0.000 claims description 4
- 239000000391 magnesium silicate Substances 0.000 claims description 4
- 235000019792 magnesium silicate Nutrition 0.000 claims description 4
- 229910052919 magnesium silicate Inorganic materials 0.000 claims description 4
- 230000001376 precipitating effect Effects 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000002023 wood Substances 0.000 claims description 3
- 239000012736 aqueous medium Substances 0.000 claims description 2
- 239000001040 synthetic pigment Substances 0.000 claims description 2
- 239000011787 zinc oxide Substances 0.000 claims description 2
- ZADYMNAVLSWLEQ-UHFFFAOYSA-N magnesium;oxygen(2-);silicon(4+) Chemical compound [O-2].[O-2].[O-2].[Mg+2].[Si+4] ZADYMNAVLSWLEQ-UHFFFAOYSA-N 0.000 claims 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 abstract description 6
- 239000002131 composite material Substances 0.000 abstract description 5
- 230000008901 benefit Effects 0.000 abstract description 3
- 230000014759 maintenance of location Effects 0.000 abstract description 3
- 239000000758 substrate Substances 0.000 abstract description 2
- 235000010216 calcium carbonate Nutrition 0.000 description 17
- 229920001131 Pulp (paper) Polymers 0.000 description 12
- 239000011230 binding agent Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000011148 porous material Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 238000009826 distribution Methods 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
- 239000012752 auxiliary agent Substances 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 235000010755 mineral Nutrition 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- 238000003490 calendering Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000002105 nanoparticle Substances 0.000 description 4
- 235000018185 Betula X alpestris Nutrition 0.000 description 3
- 235000018212 Betula X uliginosa Nutrition 0.000 description 3
- 229920003043 Cellulose fiber Polymers 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 2
- 235000011613 Pinus brutia Nutrition 0.000 description 2
- 241000018646 Pinus brutia Species 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- -1 calcium carbonate Chemical compound 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 229920006184 cellulose methylcellulose Polymers 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- YSGSDAIMSCVPHG-UHFFFAOYSA-N valyl-methionine Chemical compound CSCCC(C(O)=O)NC(=O)C(N)C(C)C YSGSDAIMSCVPHG-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- REJHVSOVQBJEBF-OWOJBTEDSA-N 5-azaniumyl-2-[(e)-2-(4-azaniumyl-2-sulfonatophenyl)ethenyl]benzenesulfonate Chemical class OS(=O)(=O)C1=CC(N)=CC=C1\C=C\C1=CC=C(N)C=C1S(O)(=O)=O REJHVSOVQBJEBF-OWOJBTEDSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 206010016807 Fluid retention Diseases 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 241000269849 Thunnus Species 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- JPNZKPRONVOMLL-UHFFFAOYSA-N azane;octadecanoic acid Chemical class [NH4+].CCCCCCCCCCCCCCCCCC([O-])=O JPNZKPRONVOMLL-UHFFFAOYSA-N 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000000404 calcium aluminium silicate Substances 0.000 description 1
- 235000012215 calcium aluminium silicate Nutrition 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- JYIMWRSJCRRYNK-UHFFFAOYSA-N dialuminum;disodium;oxygen(2-);silicon(4+);hydrate Chemical compound O.[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Al+3].[Al+3].[Si+4] JYIMWRSJCRRYNK-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 244000144992 flock Species 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000011049 pearl Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000004537 pulping Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP 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
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/63—Inorganic compounds
- D21H17/67—Water-insoluble compounds, e.g. fillers, pigments
- D21H17/69—Water-insoluble compounds, e.g. fillers, pigments modified, e.g. by association with other compositions prior to incorporation in the pulp or paper
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP 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
- D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
- D21H11/16—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only modified by a particular after-treatment
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP 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
- D21H15/00—Pulp or paper, comprising fibres or web-forming material characterised by features other than their chemical constitution
- D21H15/02—Pulp or paper, comprising fibres or web-forming material characterised by features other than their chemical constitution characterised by configuration
- D21H15/10—Composite fibres
- D21H15/12—Composite fibres partly organic, partly inorganic
Definitions
- the present invention relates to a coated fibrous web according to the preamble of claim 1.
- This kind of a fibrous web generally comprises a base web with a filler, having a pigment-containing coating layer on at least one surface.
- the present invention relates also to the method according to the preamble of claim 12 for producing a coated fibrous web.
- the printability of paper and board - properties of the printing surface and the printing process - are improved by coating the paper with different mineral coatings.
- the purpose of the coating is to cover the fibres and the fibre flocks of the paper and board and, by these measures, to decrease the roughness of the surface and the size of the pores of the surface.
- the coatings usually consist of pigments and binders, as well as of various additives.
- the coatability of paper in other words the capability of the base paper to be covered with a coating, has become even more important with the increased demand for lightweight paper grades. Although the coverage can be affected by the properties of the coating mix and the coating manner, the qualities of the base paper are also important. Good formation and smoothness as well as suitable air resistance and porosity are properties of the base paper that are the most important factors affecting the coatability, especially when good quality is aspired with a small amount of coating.
- the fibre web to be coated usually contains filler. The filler improves the formation of the paper web by filling the spaces between the fibres. Also the opacity of the web can be improved with the help of the filler.
- Finnish Patent Specification No. 100729 discloses a papermaking filler comprising porous aggregates formed by precipitated calcium carbonate particles on the surface of fines. What characterises this new kind of filler is that, according to the patent specification, the calcium carbonate is precipitated on fine fibrils produced by refining cellulose fibres and/or mechanical pulp fibres. The size distribution of the fines fraction corresponds mainly to the wire screen fraction P100.
- fillers consisting at least partly of cellulose or lignocellulose fibrils, over which light scattering material particles has been precipitated, can be used as fillers.
- These particles are typically inorganic salts precipitating in an aqueous phase, such as calcium carbonate, calcium sulphate, barium sulphate and calcium oxalate.
- the method according to the present invention is mainly characterised by what is stated in the characterising part of claim 1.
- the method according to the present invention is characterised by what is stated in the characterising part of the claim 12.
- the present invention provides considerable advantages.
- a composite filler consisting of fibrils and mineral pigments has been found to provide the base paper with properties that are, as far as coatability is concerned, better than what can be achieved with fillers that are at the present commercially available.
- the composite filler used in the present invention surprisingly can improve considerably the formation of the fibre web without impairing retention, a very smooth coating substrate can be obtained by means of the present invention.
- the smoothness of the surface can also be improved.
- the fines-based carrier fraction makes the surface of the base paper denser so that the coating does not penetrate too much into the fibre network. Due to these reasons, even a small amount of coating provides good coverage and a high quality of the coating, improving the cost efficiency.
- the filler used in the present invention is based on fibrils obtained from chemical pulp.
- chemical pulp refers to a pulp, which has been treated with cooking chemicals for delignification of the cellulose fibres.
- fibrils have been obtained by refining a pulp produced by the sulphate process or by another alkaline pulping process.
- the present invention can also be applied to modification of fibrils obtained from chemimechanical and mechanical pulp, in addition to chemical pulps.
- the average thickness of cellulose or lignocellulose fibrils is smaller than 5 ⁇ m, conventionally smaller than 1 ⁇ m.
- the fibrils are characterized by at least one of the following criteria:
- the source material for the fibrils i.e. the fines based on cellulose or other fibers, is fibrillated by beating it in a pulp refiner.
- the desired fraction may, when necessary, be separated by using a screen, but fines need not always be screened.
- Suitable fibril fractions include wire screen fractions P50 - P400.
- refiners with grooved blades are used.
- the light-scattering material particles in the filler are inorganic or organic salts that can be formed from their source materials by precipitation in an aqueous medium.
- Such compounds include calcium carbonate, calcium oxalate, calcium sulphate, barium sulphate, and mixtures thereof.
- the material particles are deposited on the fibrils.
- the amount of an inorganic salt compound in proportion to the fibril amount is approx. 0.0001 - 95 % by weight, preferably approx. 0.1 - 90 % by weight, most suitably approx. 60 - 80 % by weight, calculated from the amount of filler, and approx. 0.1 - 80 % by weight, preferably approx. 0.5 - 50 % by weight, of the paper.
- the filler is produced by precipitating a mineral pigment on the surface of fine fibrils prepared from cellulose fibres and/or mechanical pulp fibres.
- the precipitation of calcium carbonate can be carried out by feeding into an aqueous slush of fibrils an aqueous calcium hydroxide solution which possibly contains a solid calcium hydroxide, and a compound which contains carbonate ions and is at least partly dissolved in water (e.g. sodium carbonate or ammonium carbonate). It is also possible to introduce into the aqueous phase carbon dioxide gas that, in the presence of calcium hydroxide, produces calcium carbonate. There are formed string-of pearls-like calcium carbonate crystal aggregates, which are held together by fibrils, i.e.
- the diameter of the calcium carbonate particles in the aggregates is about 0.1 to 5 ⁇ m, typically about 0.2 to 3 ⁇ m.
- the fibrils correspond to wire screen fractions P50 (or P100) to P400.
- the filler at least 80 %, preferably up to 90 %, of the light scattering pigments are attached to the fibrils.
- the paper pulp is slushed by a process known per se (typically to solids content of about 0.1 to 1 %) and it is spread on the wire.
- the above-mentioned filler is added to the fibre slush most suitably in the headbox of a paper or board machine, usually in an amount of about 1 to 100 % by weight of fibres of pulp. In other words, the amount of the filler can be up to equal to - or greater than - the amount of the actual pulp.
- the pulp is webbed in a paper or board machine to form a paper or board web.
- the fibre web is dried and coated and possibly processed further, for example, by calendering.
- Coating can be carried out as single-coating or double-coating, whereupon the coating colour can be used as single-coat mixes and as so called precoating and surface-coat mixes. Also triple coatings are possible.
- the coating colour according to the present invention contains from 10 to 100 parts by weight of at least one pigment or mixture of pigments, from 0.1 to 30 parts by weight of at least one binder and from 1 to 10 parts by weight of other additives known per se.
- the typical composition of a precoating mixture is as follows: Coating pigment (for example, coarse calcium carbonate) 100 parts by weight Binder 1 - 20 % of the weight of the pigments Additives and auxiliary agents 0.1 - 10 % of the weight of the pigments Water the rest
- Water is added to the precoating mix so that the solids content is generally from 40 to 70 %.
- the composition of the surface-coat mixture or single-coat mixture is as follows: Coating pigment I (for example, fine carbonate) 10 - 90 parts by weight Coating pigment II (for example fine kaolin) 10 - 90 parts by weight Pigment total 100 parts by weight Binder 1 - 20 parts by weight Additives and auxiliary agents 0.1 - 10 parts by weight Water the rest
- Water is added to this kind of a coating colour so that the dry solids content is typically from 50 to 75 %.
- pigments that have a steep particle size distribution, so that the case at maximum 35 % of the pigment particles are smaller than 0.5 ⁇ m, preferably at maximum 15 % are smaller than 0.2 ⁇ m.
- the present invention is applicable to any pigment.
- Precipitated calcium carbonate, ground calcium carbonate, calcium sulphate, calcium oxalate, aluminium silicate, kaolin (hydrous aluminium silicate), aluminium hydroxide, magnesium silicate, talc (hydrous magnesium silicate), titanium dioxide and barium sulphate, and mixtures thereof can be mentioned as examples of the pigments.
- Synthetic pigments can also be used.
- the main pigments are kaolin, calcium carbonate, precipitated calcium carbonate and gypsum, which in general constitute over 50 % of the dry solids in the coating mix.
- Calcined kaolin, titanium dioxide, satin white, aluminium hydroxide, sodium silicoaluminate and plastics pigments are additional pigments, and their amounts are in general less than 25 % of the dry solids in the mix.
- special pigments special-quality kaolins and calcium carbonates, as well as barium sulphate and zinc oxide, should be mentioned.
- the present invention is applied especially preferably to calcium carbonate, calcium sulphate, aluminium silicate and aluminium hydroxide, magnesium silicate, titanium dioxide and/or barium sulphate, as well as mixtures thereof, in which case, especially preferably, the principal pigment in the pre-coat mixes is calcium carbonate or gypsum and in surface-coat mixes and single-coat mixes the principal pigment consists of mixtures of calcium carbonate or gypsum and kaolin.
- binders generally employed in paper production as binders in the coating colours.
- binders it is also possible to use mixtures of binders.
- typical binders include synthetic latexes made up of polymers or copolymers of ethylenically unsaturated compounds, e.g. copolymers of the butadienestyrene type, which possibly also have a comonomer containing a carboxyl group, such as acrylic acid, itaconic acid or maleic acid, and polyvinyl acetate having comonomers that contain carboxyl groups.
- the water-soluble polymers starch, CMC, hydroxyethyl cellulose and polyvinyl alcohol as binders.
- additives and auxiliary agents such as dispersants (e. g. sodium salt of polyacrylic acid), agents affecting the viscosity and water retention of the mix (e. g. CMC, hydroxyethyl cellulose, polyacrylates, alginates, benzoate), so-called lubricants, hardeners used for improving water-resistance, optical auxiliary agents, anti-foaming agents, pH control agents, and preservatives in the coating composition.
- dispersants e. g. sodium salt of polyacrylic acid
- agents affecting the viscosity and water retention of the mix e. g. CMC, hydroxyethyl cellulose, polyacrylates, alginates, benzoate
- so-called lubricants so-called lubricants
- hardeners used for improving water-resistance e. hydroxyethyl cellulose, polyacrylates, alginates, benzoate
- hardeners used for improving water-resistance
- optical auxiliary agents
- lubricants include sulpfonate oils, esters, amines, calcium or ammonium stearates; of agents improving water resistance, glyoxal; of optical auxiliary agents, diaminostilbene disulfonic acid derivatives; of anti-foaming agents, phosphate esters, silicones, alcohols, ethers, vegetable oils; of pH control agents, sodium hydroxide, ammonia; and finally of preservatives, formaldehyde, phenol, quaternary ammonium salts.
- the coating mix can be applied to the material web in a manner known per se.
- the method according to the present invention for coating paper and/or board can be carried out with a conventional coating apparatus, i.e. by blade coating, or by film coating or JET application.
- a coating layer having a grammage of 5-30 g/m 2 is formed at least on one surface, preferably on both surfaces.
- An uncoated side can be treated, for example, by web sizing.
- coated and optionally calendared cellulose-containing material webs having excellent printing properties, good smoothness and high opacity and brightness, can be produced.
- cellulose-containing material we refer to the paper or board or a corresponding cellulosic material derived from a lignocellulose-containing raw material, in particular from wood or from annual or perennial plants.
- the said material can be wood-containing or wood-free, and it can be produced from mechanical, semi-mechanical (chemimechanical) or chemical pulp. Chemical pulp or mechanical pulp may be bleached or unbleached.
- the material may also contain recycled fibers, in particular recycled paper or recycled board.
- the material may also contain recycled fibers, in particular recycled paper or recycled board.
- the grammage of the material web ranges typically from 35 to 500 g/m 2 , typically it is about 50 to 450 g/m 2 .
- the grammage of the base paper is 20-250 g/m 2 , preferably 30-80 g/m 2 .
- the grammage of which is approx. 50-70 g/m 2
- 10-20 g of coating/m 2 /side and by calendering the paper a product that has a grammage of 70-110 g/m 2 , a brightness of at least 90 %, an opacity of at least 90 % is obtained.
- An especially preferred product is a coated offset paper in which high gloss and high opacity and bulk are combined.
- the present invention is suitable also for production of coated fine paper, possibly also for those that contain mechanical pulp.
- Birch sulphate pulp was refined with a Valmet JC-01 refiner to produce pulp that is suitable for production of the filler.
- the consistency of refining was about 4 % and the total energy consumption was 343 kWh/t and the specific edge load was 0,5 J/m.
- Carbonating was performed in tap water according to the FI Patent Specification No. 100729 .
- the water slurry was obtained, the dry matter content of which was 2.22 % and total amount 248 m 3 .
- the final product had CaCO 3 content of 69.7 % and a specific surface area 10.6 m 2 /kg.
- Example 1 The product produced in Example 1 was used as a filler in coated fine papers.
- Table 2 presents the results that were obtained in the test where fine paper was produced on the pilot machine (FEX) of STFI in Sweden: Table 2.
- a base paper that has a grammage of 56 g/m 2 was produced in factory conditions for coating.
- the slush consisted of a mixture of birch pulp (74 %) and pine pulp (24 %). After refining, the SR value of the pine was 32 to 34° and that of birch was 22 to 25 °. The SR value of the pulp in the headbox was 35 to 40°.
- the wire compartment of the paper machine had a hybride wire of Valmet (Sym-former), and the wet pressing compartment consisted of a Valmet Sym-Press II that has a triple compressor and a conventional drying section.
- Nanoparticles and cationic starch (Compozil Plus: EKA NP 780 nanoparticle and EKA PL 1510 C-PAM, supplier: EKA Chemicals) were used as retention chemicals.
- the dosage amounts in the case of talc and PCC were as follows: nanoparticle 280 g/t, polymer 70 g/t, and with SuperFill: nanoparticle 280 g/t, polymer 50 g/t.
- the amounts of cationic starch and resin adhesive used were 8 kg/t and 5.2 g/t.
- the alum was administered for talc at 13 kg/t and with PCC and SuperFill at 19 kg/t.
- the coulter-oil porosity was measured from the base paper samples. No significant differences were observed in the pore size distribution with low filler contents. 75 % of all pores were in the range of 1.2 to 1.8 ⁇ m (around the maximum point). When the filler content was increased to 20 %, significant differences were observed. In the case of PCC, the median of the pore size increased as the amount of filler was increased. The median decreased and the distribution narrowed with the SuperFill filler, whereupon 75 % of the values were around 0.8 ⁇ m. The same effect can be seen with talc but in a smaller scale.
- the median of the pore size was only 60 % of the corresponding value of the PCC, and the width of the pore size distribution (75 % of values) was only 34 % of values obtained with the PCC.
- the SuperFill provides paper, the surface of which is more enclosed than the surface of the paper filled with PCC, which facilitates the coating and improves the quality of paper due to the better coverage.
- better glossier and smoother surface is obtained as the coating pigments cannot penetrate into the base paper as easily.
- the base paper described hereinbefore was coated one-side and the other side was surface-sized.
- the ABC single-blade coater of BTG was used for coating.
- the surface sizing was performed in the same unit by film transferring on the backing-roll of the coater.
- the machine velocity was 750 m/min and length of the reeler of the web was 252 cm.
- Online-coating was carried out after the fourth drying group and the coating was dried with drying cylinders (the 5 th drying group).
- the coated and calendered paper that contains SuperFill has about 5 % units better gloss and 0.1 pps units better smoothness than a corresponding paper filled with talc. This is a very good result, taking into account that the coater amounts of the SuperFill papers were even slightly smaller. The light scattering factor and brightness of the SuperFill papers were also considerably better than the corresponding papers filled with talc..
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Paper (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
Claims (16)
- Bande fibreuse revêtue, comprenant- une bande de base contenant une charge, qui comprend une couche de revêtement contenant un pigment au moins sur l'une des surfaces,
caractérisée en ce que- la charge de la bande de base est au moins partiellement constituée de fibrilles de cellulose ou de lignocellulose, sur lesquelles des particules d'un matériau diffusant la lumière ont été précipitées. - Bande fibreuse selon la revendication 1, caractérisée en ce que la charge comprend des fibrilles de cellulose ou de lignocellulose qui ont une épaisseur moyenne inférieure à 5 µm, produites par raffinage et tamisage de fibres végétales.
- Bande fibreuse selon la revendication 2, caractérisée en ce que les particules de matériau diffusant la lumière sont précipitées sur des fibrilles qui correspondent à une fraction traversant un tamis de 50 mesh et/ou ayant une épaisseur moyenne de 0,01 à 5 µm et une longueur moyenne de 10 à 1500 µm.
- Bande fibreuse selon l'une quelconque des revendications 1 à 3, caractérisée en ce que les particules de matériau diffusant la lumière sont des sels inorganiques qui peuvent être formés à partir de leurs matériaux sources par précipitation dans un milieu aqueux.
- Bande fibreuse selon la revendication 4, caractérisée en ce que les particules de matériau diffusant la lumière sont du carbonate de calcium, de l'oxalate de calcium, du sulfate de calcium, du sulfate de baryum ou leurs mélanges.
- Bande fibreuse selon l'une quelconque des revendications 1 à 5, caractérisée en ce que les particules de matériau sont précipitées sur les fibrilles.
- Bande fibreuse selon la revendication 6, caractérisée en ce que la quantité de particules de matériau diffusant la lumière par rapport à la quantité de fibrilles est de 0,0001 à 95 % en poids, de préférence d'environ 0,1 à 90 % en poids, de la manière la plus appropriée d'environ 60 à 80 % en poids, par rapport à la quantité de charge, et d'environ 0,1 à 60 % en poids, de préférence de 0,5 à 50 % en poids du papier.
- Bande fibreuse selon l'une quelconque des revendications précédentes, caractérisée en ce qu'elle est revêtue avec du carbonate de calcium, du gypse, du silicate d'aluminium, du kaolin, de l'hydroxyde d'aluminium, du silicate de magnésium, du talc, de l'oxyde de titane, du sulfate de baryum, de l'oxyde de zinc, un pigment synthétique ou leurs mélanges.
- Bande fibreuse selon l'une quelconque des revendications précédentes, caractérisée en ce que la charge, qui comprend des fibrilles de cellulose ou de lignocellulose, sur lesquelles les particules de matériau diffusant la lumière ont été précipitées, forme 10 à 100 % en poids de la charge de la bande de base.
- Bande fibreuse selon l'une quelconque des revendications précédentes, caractérisée en ce que la charge, qui comprend des fibrilles de cellulose ou de lignocellulose, sur lesquelles les particules de matériau diffusant la lumière ont été précipitées, forme 10 à 100 % en poids du matériau fibreux de la bande de base.
- Bande fibreuse selon l'une quelconque des revendications précédentes, caractérisée en ce qu'elle comprend du papier revêtu, contenant du bois ou sans bois.
- Procédé de fabrication d'une bande fibreuse, selon lequel une couche de revêtement contenant un pigment est appliquée au moins sur une surface d'une bande de base contenant un matériau fibreux, caractérisé par la formation de la bande de base à partir d'une boue du matériau fibreux, à laquelle un produit comprenant des fibrilles de cellulose ou de lignocellulose, sur lesquelles des particules d'un matériau diffusant la lumière ont été déposées, est ajouté en tant que charge.
- Procédé selon la revendication 12, caractérisé par l'utilisation d'une charge qui comprend des fibrilles de cellulose ou de lignocellulose ayant une épaisseur moyenne inférieure à 5 µm produites par raffinage et tamisage de fibres végétales.
- Procédé selon la revendication 12, caractérisé par l'utilisation d'une charge, dont les particules de matériau diffusant la lumière ont été déposées sur des fibrilles, qui correspond à une fraction qui traverse un tamis de 50 mesh et/ou ayant une épaisseur moyenne de 0,1 à 10 µm et une longueur moyenne de 10 à 1 500 µm.
- Procédé selon l'une quelconque des revendications 12 à 14, caractérisé par l'utilisation d'une charge dans laquelle au moins 80 % des particules de pigment diffusant la lumière sont attachées aux fibrilles.
- Procédé selon la revendication 12, caractérisé par le revêtement de la bande de base dans une machine à papier avec un mélange de revêtement contenant un pigment.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FI20010846 | 2001-04-24 | ||
FI20010846A FI117870B (fi) | 2001-04-24 | 2001-04-24 | Päällystetty kuiturata ja menetelmä sen valmistamiseksi |
PCT/FI2002/000341 WO2002092909A1 (fr) | 2001-04-24 | 2002-04-24 | Nappe fibreuse enduite et procede de production de ladite nappe |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1392920A1 EP1392920A1 (fr) | 2004-03-03 |
EP1392920B1 true EP1392920B1 (fr) | 2012-03-21 |
Family
ID=8561046
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP02716870A Expired - Lifetime EP1392920B1 (fr) | 2001-04-24 | 2002-04-24 | Nappe fibreuse enduite et procede de production de ladite nappe |
Country Status (10)
Country | Link |
---|---|
US (1) | US20040173329A1 (fr) |
EP (1) | EP1392920B1 (fr) |
JP (1) | JP2004525281A (fr) |
CN (1) | CN100519936C (fr) |
AT (1) | ATE550485T1 (fr) |
AU (1) | AU2002247793B2 (fr) |
CA (1) | CA2444085C (fr) |
FI (1) | FI117870B (fr) |
NZ (1) | NZ529161A (fr) |
WO (1) | WO2002092909A1 (fr) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FI115475B (fi) * | 2002-10-24 | 2005-05-13 | M Real Oyj | Menetelmä paperin ja kartongin valmistamiseksi |
FI20030976L (fi) * | 2003-06-30 | 2004-12-31 | M Real Oyj | Päällystetty pohjapaperi ja menetelmä päällystetyn pohjapaperin valmistamiseksi |
FR2879225B1 (fr) * | 2004-12-15 | 2007-02-16 | Honnorat Rech S & Services Sar | Papier brillant |
FI122674B (fi) * | 2005-06-23 | 2012-05-15 | M Real Oyj | Menetelmä kuituradan valmistamiseksi |
GB2427868A (en) * | 2005-07-04 | 2007-01-10 | Samuel Michael Baker | Cellulosic products having oleophobic and hydrophobic properties |
EP2092118A1 (fr) | 2006-12-11 | 2009-08-26 | International Paper Company | Composition d'encollage de papier, papier encollé et procédé d'encollage de papier |
SI2805986T1 (en) | 2009-03-30 | 2018-04-30 | Fiberlean Technologies Limited | Process for the production of nano-fibrillary cellulose gels |
HUE026741T2 (en) | 2009-03-30 | 2016-07-28 | Omya Int Ag | Process for the preparation of nano-fibrous cellulose suspensions |
GB0908401D0 (en) | 2009-05-15 | 2009-06-24 | Imerys Minerals Ltd | Paper filler composition |
FI124142B (fi) | 2009-10-09 | 2014-03-31 | Upm Kymmene Corp | Menetelmä kalsiumkarbonaatin ja ksylaanin saostamiseksi, menetelmällä valmistettu tuote ja sen käyttö |
DK2386682T3 (da) | 2010-04-27 | 2014-06-23 | Omya Int Ag | Fremgangsmåde til fremstilling af strukturerede materialer under anvendelse af nano-fibrillære cellulosegeler |
EP2386683B1 (fr) | 2010-04-27 | 2014-03-19 | Omya International AG | Procédé de fabrication de matériaux composites à base de gel |
GB201019288D0 (en) | 2010-11-15 | 2010-12-29 | Imerys Minerals Ltd | Compositions |
EP2460935A1 (fr) | 2010-12-01 | 2012-06-06 | SAPPI Netherlands Services B.V. | Procédé de production de dihydrate de sulfate de calcium à base de substrats de papier et/ou couleurs de revêtement |
FI20125569L (fi) * | 2012-05-28 | 2013-11-29 | Nordkalk Oy Ab | Saostettua karbonaattia sisältävän komposiittirakenteen valmistus ja käyttö |
FI126571B (fi) * | 2012-06-28 | 2017-02-28 | Nordkalk Oy Ab | Päällystyskoostumuksen käyttö maalina |
EP3362508B1 (fr) | 2015-10-14 | 2019-06-26 | FiberLean Technologies Limited | Matériau formable en feuille 3d |
EP3400333B1 (fr) * | 2016-01-05 | 2020-03-25 | Stora Enso Oyj | Procede pour la prouction d'une composite comprenant du mfc et une composite produi par le procede |
RU2727605C1 (ru) | 2016-04-05 | 2020-07-22 | Фиберлин Текнолоджис Лимитед | Бумажные и картонные продукты |
US11846072B2 (en) | 2016-04-05 | 2023-12-19 | Fiberlean Technologies Limited | Process of making paper and paperboard products |
KR102137796B1 (ko) | 2016-04-22 | 2020-07-24 | 파이버린 테크놀로지스 리미티드 | 미세섬유화 셀룰로스를 포함하는 섬유 및 그로부터 제조된 섬유 및 부직포 물질의 제조 방법 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE461860B (sv) * | 1989-02-13 | 1990-04-02 | Mo Och Domsjoe Ab | Foerfarande foer framstaellning av papper och bestruket papper varvid baspappret innehaaller precipiterat kalciumkarbonat |
US5731034A (en) * | 1990-12-04 | 1998-03-24 | Ecc International Limited | Method of coating paper |
US5223090A (en) * | 1991-03-06 | 1993-06-29 | The United States Of America As Represented By The Secretary Of Agriculture | Method for fiber loading a chemical compound |
FR2689530B1 (fr) * | 1992-04-07 | 1996-12-13 | Aussedat Rey | Nouveau produit complexe a base de fibres et de charges, et procede de fabrication d'un tel nouveau produit. |
DE4335194A1 (de) * | 1993-10-15 | 1995-04-20 | Basf Ag | Wäßrige Pigmentanschlämmungen und ihre Verwendung bei der Herstellung von füllstoffhaltigem Papier |
EP0772702A4 (fr) * | 1995-05-18 | 1998-07-01 | Huber Corp J M | Procede de preparation de fibres de papier pigmentees et de produits fibreux |
FI100729B (fi) * | 1995-06-29 | 1998-02-13 | Metsae Serla Oy | Paperinvalmistuksessa käytettävä täyteaine ja menetelmä täyteaineen va lmistamiseksi |
FI100670B (fi) * | 1996-02-20 | 1998-01-30 | Metsae Serla Oy | Menetelmä täyteaineen lisäämiseksi selluloosakuituperäiseen massaan |
FI108283B (fi) * | 1997-01-13 | 2001-12-31 | M Real Oyj | Menetelmä paperin ja kartongin päällystämiseksi |
US5952082A (en) * | 1997-07-18 | 1999-09-14 | Consolidated Papers, Inc. | Electrophotographic recording medium and method |
FI106140B (fi) * | 1997-11-21 | 2000-11-30 | Metsae Serla Oyj | Paperinvalmistuksessa käytettävä täyteaine ja menetelmä sen valmistamiseksi |
FI111401B (fi) * | 2000-01-28 | 2003-07-15 | M Real Oyj | Menetelmä kalanteroidun paperiradan valmistamiseksi sekä kalanteroitu paperituote |
FI117874B (fi) * | 2000-01-28 | 2007-03-30 | M Real Oyj | Menetelmä paperiradan päällystämiseksi sekä päällystyskoostumus |
-
2001
- 2001-04-24 FI FI20010846A patent/FI117870B/fi not_active IP Right Cessation
-
2002
- 2002-04-24 US US10/475,774 patent/US20040173329A1/en not_active Abandoned
- 2002-04-24 CA CA2444085A patent/CA2444085C/fr not_active Expired - Fee Related
- 2002-04-24 AU AU2002247793A patent/AU2002247793B2/en not_active Ceased
- 2002-04-24 CN CNB028126602A patent/CN100519936C/zh not_active Expired - Lifetime
- 2002-04-24 WO PCT/FI2002/000341 patent/WO2002092909A1/fr active IP Right Grant
- 2002-04-24 EP EP02716870A patent/EP1392920B1/fr not_active Expired - Lifetime
- 2002-04-24 NZ NZ529161A patent/NZ529161A/en not_active IP Right Cessation
- 2002-04-24 JP JP2002590163A patent/JP2004525281A/ja active Pending
- 2002-04-24 AT AT02716870T patent/ATE550485T1/de active
Also Published As
Publication number | Publication date |
---|---|
WO2002092909A1 (fr) | 2002-11-21 |
AU2002247793B2 (en) | 2008-05-01 |
FI20010846A0 (fi) | 2001-04-24 |
CN100519936C (zh) | 2009-07-29 |
NZ529161A (en) | 2005-04-29 |
CN1520484A (zh) | 2004-08-11 |
JP2004525281A (ja) | 2004-08-19 |
CA2444085A1 (fr) | 2002-11-21 |
US20040173329A1 (en) | 2004-09-09 |
ATE550485T1 (de) | 2012-04-15 |
FI20010846L (fi) | 2002-10-25 |
FI117870B (fi) | 2011-06-27 |
EP1392920A1 (fr) | 2004-03-03 |
CA2444085C (fr) | 2011-11-22 |
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