WO2012042115A1 - Procédé d'amélioration de l'aptitude au passage sur machine de bande de papier humide, utilisation de solution et papier - Google Patents

Procédé d'amélioration de l'aptitude au passage sur machine de bande de papier humide, utilisation de solution et papier Download PDF

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Publication number
WO2012042115A1
WO2012042115A1 PCT/FI2011/050842 FI2011050842W WO2012042115A1 WO 2012042115 A1 WO2012042115 A1 WO 2012042115A1 FI 2011050842 W FI2011050842 W FI 2011050842W WO 2012042115 A1 WO2012042115 A1 WO 2012042115A1
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WO
WIPO (PCT)
Prior art keywords
anionic polymer
paper web
cationic
wet paper
anionic
Prior art date
Application number
PCT/FI2011/050842
Other languages
English (en)
Inventor
Kristian Salminen
Elias Retulainen
Original Assignee
Kemira Oyj
Stora Enso Oyj
Upm-Kymmene Corporation
Kataja-Aho, Janne
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 Kemira Oyj, Stora Enso Oyj, Upm-Kymmene Corporation, Kataja-Aho, Janne filed Critical Kemira Oyj
Priority to CN201180047192.6A priority Critical patent/CN103201426B/zh
Priority to ES11770850.3T priority patent/ES2674881T3/es
Priority to BR112013007876-6A priority patent/BR112013007876B1/pt
Priority to EP11770850.3A priority patent/EP2622132B1/fr
Publication of WO2012042115A1 publication Critical patent/WO2012042115A1/fr

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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
    • D21H17/20—Macromolecular organic compounds
    • 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
    • D21H17/20—Macromolecular organic compounds
    • D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
    • D21H17/24—Polysaccharides
    • 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
    • D21H17/20—Macromolecular organic compounds
    • D21H17/33—Synthetic macromolecular compounds
    • D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/41—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
    • D21H17/42—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups anionic
    • 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
    • D21H21/00—Non-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
    • D21H21/14—Non-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
    • D21H21/18—Reinforcing agents
    • 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
    • D21H17/20—Macromolecular organic compounds
    • D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
    • D21H17/24—Polysaccharides
    • D21H17/25—Cellulose
    • 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
    • D21H17/20—Macromolecular organic compounds
    • D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
    • D21H17/24—Polysaccharides
    • D21H17/31—Gums
    • D21H17/32—Guar or other polygalactomannan gum
    • 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
    • D21H17/20—Macromolecular organic compounds
    • D21H17/33—Synthetic macromolecular compounds
    • D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/41—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
    • D21H17/44—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups cationic
    • 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
    • D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
    • D21H23/02—Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
    • D21H23/22—Addition to the formed paper
    • D21H23/50—Spraying or projecting

Definitions

  • the present invention relates to a method for improving runnability of a wet paper web, use of a solution and a paper according to the preambles of the enclosed claims.
  • the wet paper runnability may be increased by increasing the strength of the wet web.
  • a number of solutions are known for increasing the strength of the wet paper web, such as increasing the beating degree of the pulp, varying the overall furnish composition or web tension in process.
  • many of these solutions cause, at the same time, deterioration of the properties of the final produced paper or increase significantly the production costs.
  • an increase in the beating degree may increase curling and adversely affect the properties of final paper.
  • Traditional wet strength additives which are used to increase the wet strength of the dried final paper web, do not enhance strength of the wet paper web, i.e. the strength of never dried wet webs. This is because wet strength additives typically require heating and curing before they show strength improving properties. Paper machines producing paper grades whose strength before drying is a critical factor may have high efficiency but their average production speed may be significantly lower than their nominal speed. The speed of these paper machines could be raised if the strength of the wet paper web could be increased.
  • Fillers such as clay, calcium carbonate, calcium sulphate or talc are used in paper making to reduce cost of paper and to improve optical properties of paper. Fillers are added to the stock before paper machine. For coated paper grades coating pigments, which comprise the same minerals, may partly enter to the paper via the broke, which is recycled back to paper making process. The content of fillers and coating pigments is typically measured through ash content measurement by burning the stock or paper sample in 525 °C.
  • the base paper for uncoated fine paper and for coated fine paper is made from softwood and hardwood and its ash content is typically 18 - 24 %.
  • the base paper for 100 % softwood based uncoated fine paper and for coated fine paper has an ash content typically 10— 17 %.
  • An important limiting factor preventing the increase of filler content in fine papers is the wet web runnability.
  • An object of this invention is to minimise or even eliminate the disadvantages existing in the prior art.
  • An object of the present invention is to provide an effective and simple method for improving the strength of a wet paper web or the like.
  • An object of the present invention is to increase filler content of paper in order to reduce papermaking cost.
  • Typical paper according to the present invention is produced by using the method according to the invention.
  • the solution comprising an anionic polymer in dissolved form is used for improving runnability of a wet paper web by applying the solution to the web.
  • the interactions between the fibres are improved as well as the strength of the wet paper web. It is assumed, without willing to be bound by theory, that the applied anionic polymer is adsorbed or attached by the electronic interactions on the fibre surface with cationic charge.
  • the increase in wet paper web strength could be affected by the molecular level interactions between the chemicals and fibres. This may promote the amount of fibre-fibre interactions and the strength of the bonds that are formed between the fibres.
  • an anionic polymer solution to the wet paper web may enable an increase in the filler content of paper.
  • a high filler content in the base paper may be used, corresponding to ash content e.g. over 25 % for uncoated fine paper and for coated fine paper base paper made from softwood and hardwood mixture.
  • a high filler content in the base paper may be used for 100% softwood based uncoated fine paper and for coated fine paper base paper, the high filler content corresponding to an ash content over 18%.
  • An improvement in initial wet web strength and dry strength would enable ash content increase also for other paper and board grades, such as ash content increase to 5 - 17 % for newsprint grades, or ash content increase to 8 - 14 for SC and LWC base paper.
  • Improvement in strength of the initial wet paper web may also be utilised by changing to cheaper raw material mixture for the stock. For example, less old corrugated container (OCC) and more collected paper from households to make test liner or fluting board grade. The ash content of recycled fibre based fluting or test liner board may be increased over 15%.
  • OCC corrugated container
  • Another way to utilise the improved initial wet web strength is to reduce line loads at the press, which improves dry strength and decreases porosity of paper. This would be beneficial for printability.
  • the anionic polymer solution may be applied to the wet fibre web and the application may be performed in any suitable manner, for example by spraying or coating.
  • the anionic polymer solution may also be applied by using film transfer, such as film transfer to a press belt, foam layer application or feeding of anionic polymer solution from a separate headbox.
  • Preferably the application of the anionic polymer solution is performed by spraying. It has been found out that the spraying of the anionic polymer solution to the fibre web provides many surprising advantages. Spraying of the polymer solution does not influence the formation of the paper web, whereby there is no negative effects to be noticed in the final paper properties. On the other hand, it has also been noticed that the retention of the anionic polymer solution to the web is better than by addition the polymer solution to the stock.
  • the used amount of the anionic polymer can be kept low, and chemical losses may be minimised. It has been observed that when the anionic polymer solution is added by spraying, the polymer is evenly distributed through the whole web. No difference in amount of the polymer can be observed between the surfaces and the core part of the web.
  • the applying of the anionic polymer to the wet paper web does not have an effect on the density of final dry paper. This might indicate that the application of anionic polymer increases the strength of fibre-fibre bonds in the wet paper web but it might not increase the number of these bonds.
  • the spraying of the anionic polymer may increase the air permeability of the final dried paper, even by 35% on average.
  • the anionic polymer solution is a solution that comprises a dissolved anionic polymer in a solvent, typically water.
  • the anionic polymer solution may comprise the anionic polymer both in dissolved and dispersed form, as long as the amount of dissolved anionic polymer is sufficient for obtaining the desired effect.
  • the anionic polymer solution, which is used in this invention may be free from discrete polymer particles.
  • the anionic polymer solution may comprise one anionic polymer or it may comprise a mixture of different dissolved anionic polymers, for example a mixture of two or three anionic polymers.
  • This embodiment means applying to the wet paper web anionic polymer solution, which comprises a mixture of different anionic polymers, for example a mixture of two or three anionic polymers.
  • the anionicity of the polymers may be different from each other.
  • the solution may comprise two or more dissolved anionic polymers having different anionicity.
  • two or more anionic polymer solutions may be applied on the wet paper web sequentially, preferably by spraying.
  • a first anionic polymer solution is applied to the wet paper web and after this a second and optional following anionic polymer solutions are applied to the wet paper web.
  • the application is preferably performed by spraying.
  • the anionic polymer solution comprises synthetic anionic polymer, such as anionic polyacrylamide, or carboxymethyl cellulose (CMC) or other anionic high molecular weight polymers, such as anionic starch, anionic guar gum or alginate. This anionic polymer solution is applied on the wet paper web.
  • Carboxymethyl cellulose is an anionic polymer produced by introducing carboxyl methyl groups to the cellulose chain, the degree of substitution and the chain length of the cellulose backbone affecting its properties. When the degree of substitution exceeds 0.3, carboxymethyl cellulose becomes water soluble.
  • the anionic polymer solution may also be obtained by using an amphoteric polymer, provided that its net charge is anionic at the pH of the papermaking process.
  • the concentration of the anionic polymer solution is ⁇ 1 weight-%, more typically 0.05 - 1 weight-%, even more typically 0.2 - 0.6 weight-%
  • a solution of a synthetic anionic polymer is applied as the anionic polymer solution to the wet paper web.
  • the synthetic anionic polymer may, for example, be selected from the group comprising a completely or partly hydrolyzed polyacrylamide, or a homopolymer or a copolymer comprising at least one anionic monomer, such as (meth)acrylic acid, maleic acid, crotonic acid, itaconic acid, vinylsulphonic acid, 2-acrylamide-2- methylpropanesulfonic acid, styrene sulfonic acid, vinyl phosphonic acid or ethylene glycol methacrylate phosphate. Also non charged monomers can be included.
  • the synthetic anionic polymer is a copolymer of acrylamide with one or more anionic comonomers.
  • glyoxylated anionic acrylamide copolymers are suitable for use in the present invention.
  • the synthetic anionic polymer can be either in acid or in salt form, and it can be linear, branched or slightly crosslinked.
  • a copolymer means a polymer, which is composed of at least two different monomers.
  • the number of different monomers, which form the copolymer may be higher than two, for example three or four.
  • the weight average molecular weight (MW) of the synthetic anionic polymer is typically >100,000 g/mol, more typically >1 ,000,000 g/mol.
  • the application of the anionic polymer solution on the wet paper web may be performed by spraying a synthetic anionic polymer solution having a concentration in the range of 0.3 - 0.5 weight-%.
  • the solution of synthetic anionic polymer is sprayed to the wet paper web.
  • a solution suitable for use in the present invention may be obtained, for example, by dissolving a synthetic anionic polymer powder in water in order to form a 0.3 - 0.5 % w/w solution.
  • the solution may also be obtained by dissolving an emulsion or dispersion of a synthetic anionic polymer.
  • the anionic polymer may be applied, preferably by spraying, in amount ⁇ 2 g/m 2 , typically 0.05 - 1 .5 g/m 2 , more typically ⁇ 1 g/m 2 , most typically 0.05 - 1 g/m 2 , preferably 0.05 - 0.5 g/m 2 , more preferably 0.05 - 0.3 g/m 2 to the wet paper web.
  • the surface charge of natural unmodified cellulosic, lignocellulosic or wood fibres, which are used in papermaking is anionic.
  • the surface charge of the fibres is manipulated to be at least partially cationic, i.e. the fibres may have surface areas that have a cationic charge, even if they may have other surface areas that have anionic charge. This may be obtained by modifying at least part of the fibres in order to at least partially change their surface charge.
  • the surface charge of the fibres, which are used for making the paper web may be modified, partially or wholly, by adding a cationic polymer to the stock.
  • the cationic polymer, which is added to the stock may be any cationic polymer suitable to be used in the stock.
  • Cationic polymer, which is added to the stock of fibres may be selected from the group comprising chitosan, a cationised polysaccharide, such as cationic starch or cationic guar gum, or a cationic synthetic polymer, such as cationic acrylamide copolymers, vinylamine copolymers or polyamidoamine. Also glyoxylated cationic polyacrylamides may be used as cationic polymer in the present invention.
  • Cationic polymer may also be a cationic starch graft co-polymer that is described for example in US 7,786,238 B2.
  • the cationic polymer, which is added to the stock is cationic starch.
  • cationic polymer, which is added to the stock of fibres is cationic acrylamide polymer, it may be formed from water soluble ethylenically unsaturated monomers or from a monomer blend, which includes cationic monomers.
  • the cationic acrylamide polymer has an apparent intrinsic viscosity of at least 1 .0 dl/g more preferably at least 1 .5 dl/g.
  • cationic polymer may be an amphoteric polymer, provided that its net charge is cationic at the pH of the papermaking process.
  • the addition is preferably made to the thick stock, which has consistency of > 2 %, preferably 3 - 5 %.
  • Synthetic cationic polymers are typically and preferably added to the thick stock in amount of 0.5 - 5 kg/t.
  • the synthetic cationic copolymers that are added to the stock have low charge density, for example cationic acrylamide copolymers are typically low charge cationic acrylamide copolymers having charge ⁇ 1 .7 meq/g preferably ⁇ 1 .2 meq/g at pH 4.
  • the surface charge of the fibres is modified by adding cationised polysaccharide, such as cationic starch or cationic guar gum, to the stock of fibres.
  • cationised polysaccharide such as cationic starch or cationic guar gum
  • the cationised polysaccharide, such as cationic starch or cationic guar gum is preferably added to the thick stock, having, for example, consistency of 2 - 5 % between pulp storage tower and short circulation.
  • Cationic starch may be any cationic starch suitable to be used in paper making, such as potato, rice, corn, waxy corn, wheat, barley or tapioca starch. Starches having an amylopectin content > 75 % are advantageous.
  • cationic starch comprises cationic groups, such as quaternized ammonium groups, and the degree of substitution (DS), indicating the number of cationic groups in the starch on average per glucose unit, is typically 0.01 - 0.20, preferably 0.01 - 0.06.
  • cationic starch has a charge of 0.06 - 1 .04 meq/g, preferably 0.06 - 0.35 meq/g.
  • the starch may be used in amount of 2 - 20 kg/ton pulp, typically 7 - 12 kg/ton pulp.
  • the anionic polymer solution may be applied to the wet paper web when the dryness of the web is ⁇ 50 %, typically ⁇ 40 %, more typically ⁇ 30 %, most typically 8 - 15 %.
  • the pulp suspension When the pulp suspension enters the headbox and thus the paper machine, its dryness level is typically more or equal to 0.3 % and less than 2 %.
  • the first water removal from the web is driven by gravity when the web enters the wire section from the headbox. As paper travels further in the wire section, water removal is assisted by different vacuum units. After the wire section, the dryness of the paper is typically 20 %. The dryness of paper increases to 40 - 50 % during wet pressing.
  • the applying of the anionic polymer solution is preferably conducted before the last vacuum zone of the wire section, preferably by spraying.
  • the applying of the anionic polymer solution is performed to the wet paper web before press section of a paper machine.
  • the present invention is advantageous for improving strength of the wet paper web when producing wood-free uncoated and coated paper grades.
  • the present invention is also suitable for improving strength of the wet paper web when producing paper grades including super calendered (SC) paper, ultralight weight coated (ULWC) paper, light weight coated (LWC) paper and newsprint paper, but not limited to these.
  • Typical coated magazine paper, such as LWC comprises mechanical pulp around 40 - 60 weight-%, bleached softwood pulp around 25 - 40 weight-% and fillers and/or coating agents around 20 - 35 weight-%.
  • SC paper comprises mechanical pulp around 70 - 90 weight-% and long fibered cellulose pulp around 10 - 30 %.
  • the paper web may comprise fibres from hardwood trees or softwood trees or a combination of both fibres.
  • the fibres may be obtained by any suitable pulping or refining technique normally employed in paper making, such as thermomechanical pulping (TMP), chemimechanical (CMP), chemithermomechanical pulping (CTMP), groundwood pulping, alkaline sulphate (kraft) pulping, acid sulphite pulping, and semichemical pulping.
  • TMP thermomechanical pulping
  • CMP chemimechanical
  • CMP chemithermomechanical pulping
  • groundwood pulping alkaline sulphate (kraft) pulping
  • acid sulphite pulping acid sulphite pulping
  • semichemical pulping The paper web may comprise only virgin fibres or recycled fibres or a combination of both.
  • the weight of the final paper web is 30 - 800 g/m 2 , typically 30 - 600 g/m 2 , more typically 50 - 500 g/m 2 , preferably 60 - 300 g/m 2 , more preferably 60 - 120 g/m 2 , even more preferably 70 - 100 g/m 2 .
  • the paper web may comprise fibres originating from non-wood material, such as bamboo, sugar cane bagasse, hemp, wheat or rice straw.
  • the application of the anionic polymer solution to the wet paper web is preceded or followed by application of cationic or amphoteric polymer solution.
  • This kind of sequential application of polymers to the wet paper web preferably through spraying, may produce a marked improvement of dry and wet paper web strength.
  • Anionic and cationic polymer solutions may also be pre- mixed together before their application, preferably by spraying, to the wet paper web.
  • addition of a cationic polymer to the stock of fibres is not compulsory, but it may be performed.
  • polymer solution(s) of carboxymethyl cellulose (CMC), polyvinyl alcohol (PVA), modified polyvinyl alcohol, guar gum and/or chitosan are applied on wet paper web before the press section before or after applying the anionic polymer solution to the wet paper web.
  • Carboxymethyl cellulose, polyvinyl alcohol, modified polyvinyl alcohol, guar gum or chitosan may be applied one at the time or two or three of them may be applied sequentially.
  • CMC and chitosan improve the wet web strength when the web has a dryness level above approximately 55%
  • PVA improves the wet web strength also at lower web dryness levels.
  • Polyelectrolyte multilayers of anionic and cationic polymers increase the molecular contact area in the fibre-fibre joints and thus increase the strength of dry paper.
  • the layering of polymers for example two layers, may improve also the strength of the wet paper web significantly. This shows that the layering of polymers also increases the interactions between fibres in the wet state.
  • the spraying of anionic polymer to the outermost layer may reduce the adhesion between the wet web and the anionic centre roll on a paper machine. During the generation of polymer bi- or multilayers on the paper machine by spraying the amount of sprayed polymers is advantageously minimised.
  • one or more layers of chemical solutions are applied to the wet paper web before the press section or drying section.
  • a cationic polymer to the stock of fibres is not compulsory, but it may be performed.
  • Cationic polymers are as defined earlier in this text.
  • the chemical solutions are preferably applied to the wet paper web by spraying, as described in the application, but they may be applied by coating, film transfer, foam layer application or feeding from a separate headbox.
  • the chemical solution that is applied to the web e.g. by spraying, may be a solution of carboxymethyl cellulose (CMC), polyvinyl alcohol (PVA), chitosan or guar gum. Guar gum is here understood as a galactomannan.
  • the backbone of the guar gum is a linear chain of ⁇ 1 ,4-linked mannose residues to which galactose residues are 1 ,6-linked at every second mannose, forming short side-branches.
  • Guar gum may be applied to the web in form of native guar gum, anionic guar gum or cationic guar gum.
  • native, cationic or anionic guar gum may be applied to the wet paper web, which is formed without using addition of a cationic polymer to the stock.
  • native or anionic guar gum may be applied to the wet paper web, which is formed from stock into which cationic polymer, such as cationic guar gum, is added.
  • EXPERIMENTAL Example 1 Commercial never-dried bleached softwood kraft pulp from a Finnish paper mill is used as raw material. The pulp has a Canadian Standard Freeness (CSF) value of 500 ml, measured according to standard SCAN-C 21 :65.
  • CSF Canadian Standard Freeness
  • Wet handsheets having grammage of 60 g/m2 are formed by using standard for preparation of laboratory sheets with recirculated white water SCAN-CM 64:00.
  • the amount of added cationic starch is 10 kg/t (Raisamyl 135 starch DS 0.035, BASF).
  • Anionic polymer solution is sprayed onto the formed handsheets attached onto a wire with a vacuum underneath. The vacuum enhances the penetration of anionic polymer solution into the wet paper sheet during spraying.
  • the concentration of the sprayed anionic polyacrylamide (Fennopol A 8500 R from Kemira Oyj) is 0.3 % w/w consistency and mixed at room temperature over night before spraying. Reference sheets are sprayed with water.
  • the handsheets are wet pressed.
  • the wet pressing is done at two different pressure levels, 50 kPa and 350 kPa to reach two different dryness levels for the wet handsheets.
  • Wet samples are cut to a width of 20 mm with a sample length of 100 mm.
  • Wet samples are stored in an air-proof condition in a plastic bag at a temperature of 7°C in order to maintain the level of dryness.
  • A-PAM anionic polyacrylamide

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Abstract

L'invention porte sur procédé d'amélioration de l'aptitude au passage sur machine d'une bande de papier humide ou autre. Le procédé comporte l'ajout d'un polymère cationique à une pâte de fibres, la formation d'une bande de papier humide à partir de la pâte de fibres et l'application d'une solution de polymère anionique sur la bande de papier humide. L'invention porte également sur un papier obtenu par ce procédé et sur l'utilisation d'une solution comportant un polymère anionique.
PCT/FI2011/050842 2010-10-01 2011-09-30 Procédé d'amélioration de l'aptitude au passage sur machine de bande de papier humide, utilisation de solution et papier WO2012042115A1 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
CN201180047192.6A CN103201426B (zh) 2010-10-01 2011-09-30 改善湿纸幅的运转性能的方法、溶液的用途以及纸
ES11770850.3T ES2674881T3 (es) 2010-10-01 2011-09-30 Método para mejorar la fluidez de una banda continua de papel húmedo, uso de una disolución y papel
BR112013007876-6A BR112013007876B1 (pt) 2010-10-01 2011-09-30 método para melhorar operabilidade de uma rede papel úmida
EP11770850.3A EP2622132B1 (fr) 2010-10-01 2011-09-30 Procédé d'amélioration de l'aptitude au passage sur machine de bande de papier humide, utilisation de solution et papier

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US38865810P 2010-10-01 2010-10-01
FI20106021A FI125713B (fi) 2010-10-01 2010-10-01 Menetelmä märän paperirainan ajettavuuden parantamiseksi ja paperi
US61/388,658 2010-10-01
FI20106021 2010-10-01

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WO2012042115A1 true WO2012042115A1 (fr) 2012-04-05

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PCT/FI2011/050843 WO2012042116A1 (fr) 2010-10-01 2011-09-30 Méthode pour améliorer un procédé de fabrication de papier ou de carton, utilisation d'un polysaccharide, et papier
PCT/FI2011/050842 WO2012042115A1 (fr) 2010-10-01 2011-09-30 Procédé d'amélioration de l'aptitude au passage sur machine de bande de papier humide, utilisation de solution et papier

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WO2016034776A1 (fr) * 2014-09-04 2016-03-10 Kemira Oyj Composition d'encollage, son utilisation et procédé pour produire du papier, du carton, ou similaire
US9752284B2 (en) 2012-11-12 2017-09-05 Kemira Oyj Method for treating a fibre stock for making of paper, board or the like and product
US10145068B2 (en) 2014-04-29 2018-12-04 Stora Enso Oyj Process for producing at least one ply of a paper or board and a paper or board produced according to the process
WO2019057350A1 (fr) * 2017-09-19 2019-03-28 Kemira Oyj Composition polymère améliorant la résistance du papier et système additif, leur utilisation et la fabrication de produits de papier
WO2019180302A1 (fr) * 2018-03-22 2019-09-26 Kemira Oyj Composition à résistance à sec, son utilisation et procédé de fabrication de papier, de carton ou similaire
WO2022117921A1 (fr) * 2020-12-02 2022-06-09 Kemira Oyj Système de traitement pour la fabrication de papier, carton ou similaire
US11365517B2 (en) 2018-03-22 2022-06-21 Kemira Oyj Method for manufacturing a multi-layered paperboard, multi-layered paperboard and composition for use in multi-layered paperboard manufacturing
EP4036305A1 (fr) * 2021-02-02 2022-08-03 BillerudKorsnäs AB Procédé de fabrication de papier
WO2022167437A1 (fr) * 2021-02-02 2022-08-11 Billerudkorsnäs Ab Procédé de fabrication de papier

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Cited By (14)

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US9752284B2 (en) 2012-11-12 2017-09-05 Kemira Oyj Method for treating a fibre stock for making of paper, board or the like and product
US8999111B2 (en) 2012-12-28 2015-04-07 Ecolab Usa Inc. Method of increasing paper surface strength by using acrylic acid/acrylamide copolymer in a size press formulation containing starch
WO2014105494A1 (fr) * 2012-12-28 2014-07-03 Ecolab Usa Inc. Procédé d'augmentation de la résistance de surface de papier par l'utilisation de copolymère acide acrylique/acrylamide dans une formulation de presse encolleuse contenant de l'amidon
US10145068B2 (en) 2014-04-29 2018-12-04 Stora Enso Oyj Process for producing at least one ply of a paper or board and a paper or board produced according to the process
US10407831B2 (en) 2014-09-04 2019-09-10 Kemira Oyj Sizing composition, its use and a method for producing paper, board or the like
WO2016034776A1 (fr) * 2014-09-04 2016-03-10 Kemira Oyj Composition d'encollage, son utilisation et procédé pour produire du papier, du carton, ou similaire
WO2019057350A1 (fr) * 2017-09-19 2019-03-28 Kemira Oyj Composition polymère améliorant la résistance du papier et système additif, leur utilisation et la fabrication de produits de papier
US10914038B2 (en) 2017-09-19 2021-02-09 Kemira Oyj Paper strength improving polymer composition and additive system, use thereof, and manufacture of paper products
WO2019180302A1 (fr) * 2018-03-22 2019-09-26 Kemira Oyj Composition à résistance à sec, son utilisation et procédé de fabrication de papier, de carton ou similaire
US11365517B2 (en) 2018-03-22 2022-06-21 Kemira Oyj Method for manufacturing a multi-layered paperboard, multi-layered paperboard and composition for use in multi-layered paperboard manufacturing
US11427965B2 (en) 2018-03-22 2022-08-30 Kemira Oyj Dry strength composition, its use and method for making of paper, board or the like
WO2022117921A1 (fr) * 2020-12-02 2022-06-09 Kemira Oyj Système de traitement pour la fabrication de papier, carton ou similaire
EP4036305A1 (fr) * 2021-02-02 2022-08-03 BillerudKorsnäs AB Procédé de fabrication de papier
WO2022167437A1 (fr) * 2021-02-02 2022-08-11 Billerudkorsnäs Ab Procédé de fabrication de papier

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PT2622132T (pt) 2018-07-03
CN103140626A (zh) 2013-06-05
CN103201426A (zh) 2013-07-10
WO2012042116A1 (fr) 2012-04-05
CA2813148A1 (fr) 2012-04-05
ES2674881T3 (es) 2018-07-04
US20130299109A1 (en) 2013-11-14
FI20106021A (fi) 2012-04-02
FI20106021A0 (fi) 2010-10-01
EP2622131B1 (fr) 2020-02-26
CA2813148C (fr) 2018-02-06
CN103201426B (zh) 2016-05-11
EP2622132B1 (fr) 2018-04-04
FI125713B (fi) 2016-01-15
BR112013007876A2 (pt) 2019-08-27
BR112013007876B1 (pt) 2020-12-29
ES2791997T3 (es) 2020-11-06
EP2622132A1 (fr) 2013-08-07
FI20106021L (fi) 2012-04-02
BR112013007244A2 (pt) 2016-06-14
EP2622131A1 (fr) 2013-08-07

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