WO1997024489A1 - Papier haute qualite et procede de fabrication correspondant - Google Patents
Papier haute qualite et procede de fabrication correspondant Download PDFInfo
- Publication number
- WO1997024489A1 WO1997024489A1 PCT/JP1996/003838 JP9603838W WO9724489A1 WO 1997024489 A1 WO1997024489 A1 WO 1997024489A1 JP 9603838 W JP9603838 W JP 9603838W WO 9724489 A1 WO9724489 A1 WO 9724489A1
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- WO
- WIPO (PCT)
- Prior art keywords
- paper
- metal roll
- pulp
- paper according
- water
- Prior art date
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Classifications
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- 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
- D21H25/00—After-treatment of paper not provided for in groups D21H17/00 - D21H23/00
- D21H25/005—Mechanical treatment
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21G—CALENDERS; ACCESSORIES FOR PAPER-MAKING MACHINES
- D21G1/00—Calenders; Smoothing apparatus
-
- 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
- D21H21/16—Sizing or water-repelling 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
- 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
- D21H21/20—Wet strength 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
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/06—Alcohols; Phenols; Ethers; Aldehydes; Ketones; Acetals; Ketals
-
- 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
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/07—Nitrogen-containing 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
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/37—Polymers of unsaturated acids or derivatives thereof, e.g. polyacrylates
- D21H17/375—Poly(meth)acrylamide
-
- 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
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/47—Condensation polymers of aldehydes or ketones
-
- 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
- D21H19/00—Coated paper; Coating material
- D21H19/10—Coatings without pigments
- D21H19/14—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
-
- 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
- D21H19/00—Coated paper; Coating material
- D21H19/10—Coatings without pigments
- D21H19/14—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
- D21H19/18—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising waxes
-
- 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
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/38—Coatings with pigments characterised by the pigments
- D21H19/40—Coatings with pigments characterised by the pigments siliceous, e.g. clays
Definitions
- the present invention relates to paper having excellent dimensional stability and rigidity and having high tensile strength (referred to as high-performance paper).
- the present invention relates to a method for producing a paper in which two or more papers are laminated, wherein a paper having an arbitrary thickness can be easily obtained without using an adhesive or the like.
- paper is finished by beating pulp to make it acidic or neutral, and subjecting it to a super calender treatment to obtain smoothness and luster.
- various additives such as sizing agents, paper-strengthening agents, drainage agents, fillers, and dyes are appropriately added to the papermaking raw materials.
- a multi-stage super calender is used to increase the tension of the paper, and the structure is such that metal rolls and elastic rolls are alternately arranged. Obtained through moderately moistened paper. The temperature of the roll at that time is about 80 to 120 ° C.
- Machine calendering and super-calendering of paper is a force described in Japanese Patent Application Laid-Open No. H5-24-27896. These calenders are generally not operated at such high pressures, especially super calenders.
- calenders In general, is a combination of a metal roll and an elastic roll. The elastic roll is soft and easily deformed.
- Paper is composed based on cellulose fibers. Paper cellulose has a strong crystalline structure and an amorphous structure, and water penetrates into the amorphous structure to expand fibers, and conversely, water escapes and contracts. In paper, the overall expansion and contraction due to the change in moisture occurs when the expansion and contraction of the fiber spreads over the entire surface through interwoven bonds.
- a polyolefin polymer compound such as polyethylene or polypropylene is laminated on paper, or a compound such as phenolic resin is impregnated into paper and cured.
- Replacement form (Rule 26) Is crosslinked to reduce the expansion and contraction of the paper.
- paper laminated with a polyolefin-based polymer compound has a strong coating layer, and there is a problem such as pulp fibers remaining in flocks when recovering waste paper. There was a problem in terms of resource and resource reuse. Further, in the method of laminating a polyolefin-based polymer compound on paper, since the polyolefin resin is a thermoplastic resin, the resin is melted when heat is applied, resulting in poor heat resistance.
- the lamination methods include ⁇ ⁇ et lamination method, hot-melon lamination method, dry lamination method, and extrusion method. It is roughly classified into four types: coating and lamination method. Pet lamination method, dry lamination method, extrusion coating and lamination method are applied for lamination between papers. .
- a water-soluble adhesive or a water-dispersible adhesive is applied, bonded while wet, integrated, and then removed to remove moisture contained in the adhesive. It is a method of evaporating, drying and winding up after bonding is completed. Since this method uses a water-based adhesive, water must be evaporated and a drying step is required.
- a solvent-type adhesive is applied and dried first, and then a sheet is adhered to the adhesive surface. This method also requires a step of drying the solvent.
- This method involves extruding as a hot-melt film, placing it on a continuous substrate such as paper, placing the paper to be bonded on top of it, crimping and joining, cooling, and cooling and solidifying the molten film.
- Both the wet lamination method and the dry lamination method require a drying step, and require the use of an adhesive, so a coating device is required, and their maintenance and cleaning are difficult.
- Extrusion coating ⁇ The lamination method requires equipment to extrude hot melt resin.
- An object of the present invention is to provide a high-tensile paper having excellent elasticity and rigidity.
- An object of the present invention is to provide a paper which is excellent in dimensional stability and is capable of collecting used paper.
- An object of the present invention is to provide paper which is easy to handle, has excellent dimensional stability, and has excellent rigidity.
- An object of the present invention is to provide a method for producing a paper in which two or more papers having any thickness are easily laminated without using an adhesive.
- the first invention of the present invention is characterized in that paper is passed under a pressurizing condition of a linear pressure of 200 to 250 OkgZcni through a nib portion formed by a metal roll and a metal roll. Related to the paper manufacturing method.
- a method in which, after the cellulose fibrous agent is contained in paper, the paper is applied to a nib formed by a metal roll and a metal roll with a linear pressure of 200 to 25.
- the present invention relates to a paper characterized in that the paper has been passed under a pressure of 0 kgZcm.
- a fourth invention of the present invention is characterized in that two or more papers are passed through a nip portion composed of a metal roll and a metal roll under a pressure condition of a linear pressure of 500 to 250 OkgZcBi.
- the present invention relates to a method for producing paper in which two or more papers are laminated.
- the present inventors are rich in elasticity, rigidity and dimensional stability
- the high-strength paper thus obtained can be used as a substitute for various film supplies, and is rapidly degraded by microorganisms in the natural environment, so that it does not pollute nature. It has a great feature of saying.
- nip line pressure is less than 20 O kgZcm
- film-shaped paper cannot be obtained, and if it exceeds 250 O kgZcni, a phenomenon occurs in which only a part of the paper stretches, and the product value becomes lower. Will be gone.
- paper is passed under a pressurized condition of 200 to 250 O kgZcro through a nip formed by a metal roll and a metal roll, but of course, a paper having a plurality of nips may be used. Included. When the paper passes through a plurality of nibs, the change in paper thickness becomes small, but the paper properties such as air permeability change.
- the paper to be treated in the present invention contains fine paper, medium paper, and the like made by a fourdrinier multi-cylinder paper machine, a fourdrinier Yankee paper machine, a round net paper machine, and the like.
- the filler examples include kaolin, talc, clay, calcium carbonate, calcined clay, titanium oxide, diatomaceous earth, fine anhydrous silica, activated clay, zinc oxide, aluminum oxide, aluminum hydroxide, zinc sulfate, barium sulfate, and silicon dioxide.
- inorganic pigments such as colloidal silica, and organic pigments such as urea formalin-based resin filler, nylon powder, and polyethylene powder.
- a method for impregnating the resin a method such as a size press can be used.
- a method of coating a blade coater, an air knife coater, a gravure coater, a roll coater, or the like can be used as appropriate.
- any device that can satisfy the pressurizing condition of 200 to 250 O kgZcni in the nip portion can be appropriately adopted.
- the apparatus satisfying the pressurizing condition include a two-stage calender, a multi-stage calender, and the like.
- the present inventors have found that the paper subjected to the high-pressure treatment is inferior in dimensional stability to the paper before the treatment. Therefore, we examined the possibility of preventing moisture from penetrating inside the paper by applying a moisture-proof resin on the paper and obtaining paper with good dimensional stability. Or later, it was found that the effect was particularly remarkable when a moisture-proof resin was applied on paper.
- the dimensional stability referred to here is the degree of elongation when the paper is immersed in water, and refers to the elongation in water.
- the preferred water elongation of the paper obtained in the present invention is 2% or less in the transverse direction, particularly preferably in the range of 0 to 1%.
- the measurement of the infiltration elongation was performed by a method based on the B method of J.TAPPI No. 27.
- the coating equipment is not particularly limited, but includes an air knife coater, a bar coater, a roll coater, a blade coater, It can be arbitrarily selected from a gate roll coater or the like.
- the coating amount of the one surface of the coating layer in the present invention is preferably from 3 ⁇ 5 0 g / m ⁇ 1 0 ⁇ 3 0 gZm 2 is good. Incidentally 3 GZni effect is not exerted is less than 2, 5 0 g / D1 2 by weight, the effect is not desirable economically it becomes saturated.
- the wax used in the present invention is an ester of a long-chain fatty acid and a long-chain alcohol.
- Waxes include vegetable waxes, animal waxes, petroleum waxes, mineral waxes, and synthetic waxes.
- Vegetable waxes include, for example, carnauba wax, candelilla wax, wood wax, baby wax, polycury wax, Fire wax, palm wax, sugar wax, cotton wax, rice oil wax, cocoa butter wax and the like.
- Animal waxes include, for example, honeybox, insect box, box, wool box and the like.
- Examples of petroleum wax include paraffin wax and microcrystalline wax.
- mineral wax include montan wax, ozokerite, and pete wax.
- the paraffin box is preferable.
- the shellac used in the present invention is obtained by purifying a resin-secreted substance secreted by the giant larvae of the larvae having a body length of about 0.6 to 0.7 mra.
- Lackaigala is a major production area in the subtropical region of India and Thailand, and is distributed in China, Indonesia, Sri, Vietnam and other countries.
- Rack larvae are bred by tying twigs with black larvae to leguminous plants and mulberry plants, and after the black larvae suck up the sap, they release a resinous material that solidifies by air.
- a product obtained by crushing, washing with water, and purifying is used.
- Refining methods include the hot-melt method, the soda method, and the solvent extraction method.
- the hot-melt method is a method in which the resin attached to the branches is crushed, washed with water, the resin is put into a cotton bag, and the material squeezed out of the bag is stretched thinly. It is.
- the soda method is a method of dissolving the resin, which has also been pulverized and washed with water, in soda ash or caustic soda solution, removing contaminants from the solution, then precipitating with a dilute acid solution, washing with water, and drying.
- the solvent extraction method is a method in which a crushed and washed resin is dissolved in an alcohol-based solvent, filtered, and then the solvent is recovered and purified.
- the shellac used in the present invention depends on the purification method, and its components are slightly different from each other.
- valeric acid, jaralic acid, and laccijaralic acid are used as the main resin acid components, and the carboxyl groups of this resin acid and the other resin acids are used. These are mainly composed of the ones in which the hydroxyl groups are ester-bonded.
- wax components mixed esters of milliserial coal, seryl alcohol, laxeryl alcohol, etc. and lignocellic acid, laccelic acid, stearic acid, palmitic acid, etc. are mixed, and laccaic acid, erythrolaccin, desoxyerythrothrate Lakcin etc. are included.
- a solvent extraction method is preferred in view of purity and quality.
- this resin Since this resin has the ability to dissolve in water, there is no particular problem when recovering waste paper. This resin is tasteless, odorless, and non-toxic, and has no adverse effects on the environment. Therefore, due to the dimensional stability obtained by providing this resin layer on paper, paper does not pose a problem when recovering waste paper.
- wetting agents may be used in the shellac coating solution.
- silane coupling agent, titanate-based coupling agent, and aluminum-based coupling agent used in the present invention can be chemically bonded to each other in an inorganic-organic composite material system, or can be accompanied by a chemical reaction. It is used to enhance the transparency, heat resistance, water resistance, and mechanical strength of inorganic-organic composite materials. In the present invention, it acts to enhance the affinity between the synthetic resin and the fulocylate compound and to improve the moisture-proof property.
- Examples of such coupling agents include vinyltrimethoxysilane containing Si in the hydrophilic group, 7 -glycidoxypropyldimethoxysilane, aglycidoxypropyltrimethoxane, aglycidoxypropyltriethoxysilane, and methacryloxyprol.
- Silane coupling agents such as virutrimethoxysilane, N- /?
- Acetoa containing A 1 in the hydrophilic group examples include aluminum-based coupling agents such as lucoxyaluminum diisopropylate.
- Examples of the method of treating the fuurocate compound with such a coupling agent include an integral blend method and a pretreatment method.
- the integral blending method is a method in which a force coupling agent is directly added to a paint containing a ferrosilicate compound and a synthetic resin.
- the pretreatment method is a method in which a ferrosilicate compound is previously treated with a coupling agent.
- the amount of the cupping agent to be added is 0.1 to 5 parts by weight, preferably 0.5 to 2 parts by weight, based on 100 parts by weight of the fluorate compound. If the addition amount is less than 0.1 part by weight, the coating of the fulocyate compound surface with the coupling agent becomes insufficient, which is not preferable.If the addition amount exceeds 5 parts by weight, the effect of the coupling agent reaches a plateau. It is uneconomical.
- the fluoric acid salt compound used in the present invention is a substantially flat crystalline substance having an average particle diameter of several m or more, and an average particle diameter of 3 ZD! ⁇ 100 jm, preferably 5 // ⁇ ! ⁇ 50.
- the aspect ratio of the furokerate compound is preferably from 5 to 200.
- the aspect ratio in the present invention is obtained by dividing the average particle diameter of the fulocylate compound by the thickness.
- the fluorate compound used in the present invention is plate-like or flaky, and has a clear cleavage.
- clay minerals such as mica, pyrophyllite, talc, shale, septeite, serpentine, and stilp nomelane. Of these, mica and talc are preferred.
- Mica includes muscovite (mascovite), sericite (sericite), phlogopite (furocopite), biotite (biotite), fluorophlogopite (artificial mica), red mica, soda mica, Examples include vanadin mai, illite, chinmai, paragonite, and brittle mica. The most preferred of these are muscovite and sericite.
- Examples of the synthetic resin used in the present invention include styrene-butadiene copolymer (S B
- SBR acrylic styrene copolymer, methacrylate butadiene copolymer, vinyl acetate crotonate copolymer, styrene butyl methacrylate acrylate copolymer, etc.
- SBR is most suitable because the coating layer is less likely to crack due to cracking.
- Other copolymerizable monomers can be used without impairing the purpose of the present invention.
- Copolymerizable monomers include aromatic vinyl monomers such as a-methylstyrene, vinyltoluene, and p-tert-butyltoluene, methyl (meth) acrylate, ethyl (meth) acrylate, and methylacrylate 2 —Ethylhexyl, (meth) acrylic acid ester monomers such as (n) -octyl (meth) acrylate, glycidyl esters of ethylenically unsaturated acids such as (meth) glycidyl acrylate, (meth) acrylamide, N —Methylol (methyl) (meth) acrylamide-based monomers such as acrylamide
- the mixing ratio of the synthetic resin and the ferrosilicate compound is preferably 70 to 30/70 in terms of solid ratio. If the content of the fluorate compound is less than 30%, the number of layers formed by the fuokerate compound is reduced, or the distance between the fluorate compound and the fluorate compound is too large, resulting in insufficient moisture resistance. Therefore, it is necessary to reduce the amount of coating, which is uneconomical. Further, the composition tends to cause blocking. If it exceeds 70%, the number of voids between the synthetic resin and the furosilicate compound in the coating layer will increase, and the moisture resistance will decrease.
- the present inventors impregnated the paper with the cellulose fiber bridging agent and then applied the paper to a nip formed by a metal roll and a metal roll with a linear pressure of 200-200. It has been found that a paper having a tensile strength of 1.2 or more and excellent in dimensional stability can be obtained by heating and curing under a pressure condition of 250 O kg / cB.
- the crosslinker between the cellulose fibers and the glycols react with each other to form a crosslinked structure and suppress the expansion and contraction of pulp magnetic fibers. Also, since the coating liquid contains glycol amount, it quickly penetrates the paper surface during coating, and the coating does not stay on the surface, preventing transfer of the coating liquid during high-pressure treatment in the next process be able to.
- the cross-linking agent between cellulose fibers has two or more groups in one molecule that react or form a hydrogen bond with a hydroxyl group of cellulose, and cross-links between cell mouth fibers.
- R 2 represents H or an alkyl group having 1 to 5 carbon atoms; R 3 and R 4 represent H or CH 3 )
- R 5 and R e represent an alkyl group having 1 to 5 carbon atoms; R 3 and R 4 represent H or CH 3
- Examples of the compound having an N-methylol group include an initial reaction product of urea-formaldehyde and an alkylene diamine. The initial reactants of urea-formaldehyde are listed. Further, a crosslinking agent having a cyclic structure is also preferable. Substances in which these are partially N-alkoxymethylized for the control of stability and reactivity are also preferable.
- -NR- R is an alkyl group, an alkoxy group
- Replacement example paper (Rule 2 6) Ruacetylene diurea, dimethylol acetylene diurea, dimethylol piperazine, trimethylol isocyanurate, dimethylol isocyanurate, tetramethylol melamine, trimethylol melamine, dimethylol melamine, tetramethylol guanamine, trimethylol guanamine, dimethylol guanamine And others.
- Examples of the compound represented by the general formula (3) include dimethylolethylene urea, dimethyloldihydroxyethyleneurea, dimethylolpropyleneurea, 4-methoxy-5,5'-dimethyl-N, N-dimethylolpropyleneurea purple, Methylol-peron, dimethylolalkyltriazone, 1-methylol-1-3-methyloxymethyl-4,5-dihydroxyethylene urea, 1-methylol-13-methoxymethyl-4- 4-methoxy-5-hydroxyethylene urea, 1-methylol 1-3-Methoxymethyl-4-hydroxy-15-methoxyethyleneurea.
- Examples of the compound represented by the general formula (1) include 1.3-dimethyl4.5-dihydroxyethylene urea, 1,3-dimethyl-4,5-dimethoxyethylene urea, and 4-hydroxy-5-methyl Examples include toxylene ethylene urea, 4,5-dihydroxyethylene urea, and 4.5-dimethoxy ethylene urea.
- Examples of the compound represented by the general formula (2) include 1.3-dimethoxymethyl-1,4,5-dihydroxyethylene urea, 1,3-dimethoxymethyl-4-hydroxy-15-methoxyethylene urea, 3-dimethoxymethyl-4,5-dimethylmethoxyurea.
- a cyclic urea compound and a specific ethylene copolymer such as an ethylene-vinyl acetate copolymer, an ethylene monoacetate-vinyl chloride copolymer, an ethylene monovinyl acetate-acrylate copolymer, and styrene It is more effective to use a monobutadiene copolymer, a homopolymer of (meth) acrylamide or a copolymer with another vinyl monomer in combination. Also, reactive polymers such as methylolated polyacrylamide are effective.
- the epoxy compound used in the present invention is preferably of a water-soluble type.
- water-soluble epoxy compounds include ethylene glycol, polyethylene glycol, and propylene.
- the coating liquid permeates the paper surface quickly without remaining on the surface.
- glycols include propylene glycol, polypropylene glycol, dipropylene glycol, methylene glycol, 1,4-butanediol, 2,3-butanediol, 1,5 pentanediol, triethylene glycol, polyethylene glycol and the like.
- dipropylene glycol has excellent wettability and permeability to paper having a large surface size.
- the mixing ratio of the glycols and the cellulose fiber bridging agent depends on the size of the paper to be coated or impregnated, but it is usually preferably 10 to 400% based on the amount of non-precipitates of the initial condensate. , 25-250% is more preferred.
- catalysts include acids such as hydrochloric acid, sulfuric acid, borofluoric acid, acetic acid, glycolic acid, maleic acid, lactic acid, citric acid, tartaric acid, and oxalic acid, magnesium chloride, magnesium nitrate, magnesium borofluoride, and borofluoric acid.
- acids such as hydrochloric acid, sulfuric acid, borofluoric acid, acetic acid, glycolic acid, maleic acid, lactic acid, citric acid, tartaric acid, and oxalic acid
- magnesium chloride, magnesium nitrate, magnesium borofluoride, and borofluoric acid include metal salts such as zinc chloride, zinc chloride, zinc nitrate, sodium bisulfate, ammonium chloride, hydrochloride of organic amine, hydrochloride of alkanolamine and the like are used alone or in combination. These compounds are supplied to the paper by internal addition, impregnation or coating, and the effect of dimensional stability can be obtained by
- crosslinking agents 2 to 50% by weight based on pulp, preferably
- water-soluble (meth) acrylamide copolymers have an effect on the dimensional stability of paper.
- the monomers that form these (meth) acrylamide copolymers include (meth) acrylamide monomers, cationic monomers, hydroxyalkyl (meth) acrylate monomers, hydrophobic unsaturated vinyl monomers and It is a carboxyl group-containing monomer, and the copolymer is composed of three or more of these monomers.
- (meth) acrylamide monomers include, for example,
- Examples of the cationic monomer include 2- (meth) acryloyloxyshethyl trimethylammonium chloride, 2- (meth) acryloyloxyshethyltrimethylammonium chloride, 2- (meta) ) Acryloyloxyshethyltriethylammonium bromide, 3- (meth) acryloyloxypropyldimethylethylammonium chloride, 3-methacryloyloxy2-hydroquinopropyl propyltrimethylammonium Muchloride, 3-methacryloyloxy 2-hydroxypropylmethyl gethylammonium chloride, 3-methacryloyloxy 2-hydroxypropyl trimethyl ammonium chloride, 3-acrylamide propyl trimethyl ammonium Dumchloride, 2- (meth) acryloylaminoethyl trime L-ammonium chloride, 3- (meth) acryloylamino-l 2-hydroxypropyltrimethylammonium chlor
- hydroxyalkyl (meth) acrylate-based monomer examples include, for example, hydroxyshethyl- (meth) acrylate, 2-hydroxypropyl-1- (meth) acrylate, 2-hydroxybutyl-1- (methyl) acrylate, 2- Hydroxy 3-methyl propyl mono (meth) acrylate, ⁇ -hydroxy poly (ethyleneoxy) acrylate (meth) acrylate, ⁇ -hydroxy poly (propyleneoxy) mono (meth) acrylate, ⁇ -methoxy poly ( Ethyleneoxy) (meta) ac
- hydrophobic unsaturated vinyl monomer examples include methyl (meth) acrylate, (methyl) ethyl acrylate, (meth) atalinoleic acid ⁇ -propyl, (meth) isopropyl acrylate, (meth) acryloic acid ⁇ - Butyl, tertiary butyl (meth) acrylate, styrene monomers such as mono-2-ethylhexyl (meth) acrylate, styrene, vinyltoluene, ⁇ -methylstyrene, organic acid vinyl esters such as vinyl acetate, acrylonitrile And nitriles such as methacrylonitrile; halogenated olefins such as vinyl chloride and vinylidene chloride;
- the molecular weight of the copolymer in the present invention may be in the range of about 500 to 300,000, but is preferably in the range of about 10,000 to 200,000.
- a (meth) acrylamide copolymer and a polyhydric aldehyde are used in combination, the dimensional stability of the paper is excellent.
- polyvalent aldehydes include glyoxal, malonaldehyde, succinic aldehyde, glutaraldehyde, and the like.
- a water-soluble polymer or a sizing agent is used in combination with these cellulose fiber interstitial agents, it is more effective in dimensional stability.
- Water-soluble polymers include PVA, starch, oxidized starch, polyacrylamide resin, etc., but various plant gums, sodium alginate, carboquin methylcellulose, methylcellulose, chitosan, glue, casein, polyvinyl acetate, latex And the like also have an effect.
- sizing agent a synthetic sizing agent such as styrene or olefin is effective, but an alkyl ketene dimer sizing agent is particularly preferable.
- the equipment for coating or impregnating the coating liquid of the present invention is not particularly limited.
- Examples of the coating equipment include an air knife coater, a bar coater, a roll coater, a blade coater, and a gate roll coater. Press press
- Coated or impregnated amount of the coating liquid of the present invention is preferably 5 ⁇ 6 O gZn 2, more preferably 8 ⁇ 5 O gZ m 2. If the amount is less than 5 gZm 2 , the effect will not be exhibited, and if it exceeds 60 g / m 2 , the effect will be saturated, which is not economically preferable.
- any method can be used for drying the coated or impregnated citrus fruit. It is necessary. Generally, the drying temperature is 50 to 90, and it is preferable to send a large amount of air to dry.
- auxiliaries such as wetting agents and preservatives can be used as long as the performance is not adversely affected.
- pigments such as calcium carbonate and titanium oxide can be appropriately used as long as the performance is not hindered.
- the paper coated or impregnated with the coating liquid of the present invention is passed through a nip formed by a metal roll and a metal roll under a pressure condition of 200 to 250 OkgZcm.
- a nip formed by a metal roll and a metal roll under a pressure condition of 200 to 250 OkgZcm.
- voids between the pulp fibers are extremely reduced, and a high-strength paper is obtained.
- the nip line pressure is less than 20 O kgZcni, the desired effect cannot be obtained, and if it exceeds 250 O kg / cm, only a part of the paper will be stretched, and the commercial value will decrease. It will be gone.
- the heating conditions for heat curing after passing the paper are usually about 80 to 200 ° C., preferably about 100 to 160 ° C., and about 1 to 120 minutes, preferably about 5 to 6 minutes. 0 minutes is good.
- the water content of the paper to be bonded is preferably 2 to 15%. Further, if water is supplied to at least one of the bonding surfaces to wet the surface, the bonding effect at the time of bonding is further improved.
- the water supply is preferably between 1 and 1 O gZra 2 .
- As a method for supplying water there is a method in which water is applied to at least one of the bonding surfaces, or a method in which the water is sprayed or sprayed.
- the present inventors have studied a method of obtaining a laminated paper by bonding a plurality of papers by a simple method without using a drying step, and as a result, by passing the paper between metal rolls under high pressure conditions, It has been found that a laminated paper can be obtained without using an adhesive.
- the nip linear pressure between the metal rolls is less than 50 O kgZcni, the desired effect of the present invention cannot be obtained. If the nip linear pressure exceeds 250 OkgZon, only a part of the paper will be stretched. However, uniform laminated paper cannot be obtained.
- the bonding effect is further improved.
- the amount of water is preferably 1 ⁇ 1 OgZffi 2, more preferably 2-58 111 2.
- Coating methods such as bar coater, gravure coater, roll-copper, etc., water spraying, steam As a spraying method, a general spraying device, a humidifying device, or the like can be used.
- the temperature of the metal roll when water is applied, sprayed, or steamed is preferably 150 ° C.
- the paper having substantially no adhesive on the surface as referred to in the present invention includes, for example, high quality paper, medium quality paper, single-side coated paper and the like. It should be noted that surface-sized paper is also included in the present invention. Also, by increasing the number of sheets to be laminated or selecting the thickness of the paper to be laminated, a laminated paper having an arbitrary thickness can be obtained. Usually, the number of sheets to be stacked is preferably 2 to 200 sheets. Normally, the thickness of one sheet of paper before bonding is preferably 20 to 100 ⁇ m, and the thickness of the paper after bonding is usually 20 to 250 im.
- the laminated paper having a smooth surface and high air permeability can be obtained.
- the roll temperature during bonding is high, the paper temperature after passing the paper has risen, so it is advisable to cool the bonded paper with a cooling roll or the like to reduce the temperature of the paper.
- the present invention is obtained by passing paper under a pressurized condition of 200 to 250 OkgZcra through a nip formed by a metal roll and a metal roll.
- the pulp to be used is not particularly limited, and chemical pulp such as commonly used softwood bleached kraft pulp (hereinafter NBKP) or hardwood bleached kraft pulp (hereinafter LBKP), GP, BC TMP, MP, TMP, etc. Pulp obtained from non-wood raw materials such as mechanical pulp, hemp pulp, and kenaf, and pulp such as DIP are used. In addition, synthetic valves are used. Examples of the synthetic pulp include vinylon, nylon, polyethylene terephthalate, polyethylene, polypropylene, poly (meth) acrylate, polyurethane, and polystyrene.
- chemical pulp such as commonly used softwood bleached kraft pulp (hereinafter NBKP) or hardwood bleached kraft pulp (hereinafter LBKP), GP, BC TMP, MP, TMP, etc. Pulp obtained from non-wood raw materials such as mechanical pulp, hemp pulp, and kenaf, and pulp such as DIP are used. In addition, synthetic valves are used. Examples of
- softwood pulp has excellent strength. Dimensional stability, curl, etc. are inferior to hardwood pulp.
- the ratio of the softwood pulp to the total pulp is preferably less than 50% by weight.
- the beating degree of the pulp used in the present invention is preferably a Canadian standard and water degree (hereinafter, CSF) of 35 Oral or more, and unbeaten pulp can also be used. If pulp with a CSF of less than 35 Oml is used, curl, dimensional stability, paper habit, etc. of the resulting paper will be poor. In addition, it is not preferable because the re-disintegration property at the time of recovery of used paper is not good. In addition, when paper with less than 50% by weight of softwood pulp in the total pulp is used, the elasticity and rigidity are excellent when the beating degree of the pulp is 35 Oml or more in Canadian standard water content. In addition, a high-stress film-shaped paper having excellent dimensional stability can be obtained.
- CSF Canadian standard and water degree
- the pulp raw material adjusted as described above is paper-made by a fourdrinier multi-cylinder paper machine, a fourdrinier yanky paper machine, a round mesh paper machine or the like. If the paper thus obtained is immersed in water, it will quickly return to the state before the high-pressure treatment. This can be treated in the waste paper recovery process in the same way as ordinary paper. In the natural environment,
- the internal sizing agent and the external sizing agent for paper used in the present invention are not particularly limited, and rosin-based sizing agents, starch, PVA, and the like can be appropriately used.
- a paper strength agent such as polyamide epichlorohydrin resin
- the infiltration elongation tends to be good.
- the water content of the paper is preferably 2 to 15%, more preferably in the range of 5 to 10%.
- the roll temperature at the time of high-pressure treatment of paper is preferably 20 ° C to 300 ° C. If the temperature of the roll is lower than 20 ° C, the temperature of the roll is affected by the outside air temperature.
- the optimal temperature range of the roll temperature varies depending on the paper passing speed, so the amount of heat transferred to the paper changes.Therefore, even at temperatures below 300 ° C, blisters may occur if the paper passing speed is slow. If it exceeds C, the moisture in the base paper becomes a gas at a stretch, and the volume expands rapidly between the paper layers, causing the paper layer to partially peel off, causing a blister phenomenon in which the surface swells, and uniform paper is obtained. It is hard to be.
- the paper passing speed in the present invention is closely related to the temperature and cannot be determined strictly, but is preferably 10 to 50 minutes. By the way, if it exceeds 50 ⁇ / min, the temperature and pressure transmitted to the paper are not enough, and it is difficult to obtain the desired effect.
- rigidity was represented by the return value of bending. This was measured using a Gurley stiffness tester to measure the force with which the sample was bent and returned. The greater the rigidity of the sample, the greater this bending return value.
- This paper was passed through a nib formed by a metal roll and a metal roll under the conditions of a linear pressure of 500 kgZcm and a metal roll temperature of 100 ° C.
- the thickness of the obtained paper was 97 m.
- Example 1 the processing conditions linear pressure 50 Ok g / cni, except that the temperature 175 ° C was conducted in the same manner as in Example 1..
- the paper thickness of the obtained paper was 94 / m.
- Example 1 was repeated in the same manner as in Example 1 except that the processing conditions were set to a linear pressure of 750 kg / cm and a temperature of 175 ⁇ .
- the thickness of the obtained paper was 94 / zm.
- Example 1 was repeated in the same manner as in Example 1 except that the processing conditions were set to a linear pressure of 100 OkgZcnK and a temperature of 175 ° C. The thickness of the obtained paper was 94 / zm.
- Example 5
- Example 1 the paper was treated in the same manner as in Example 1 except that the paper moisture was changed to 13% and the processing conditions were changed to a linear pressure of 25 OkgZcnu and a temperature of 10 (TC.
- the obtained paper had a thickness of 104 ⁇ . there were.
- the processing was performed in the same manner as in Example 1 except that the paper moisture was set to 13% and the processing conditions were set to a linear pressure of 100 Okgcm and a temperature of 100 ° C.
- the thickness of the obtained paper was 98 m.
- the paper obtained by processing in Example 6 was further subjected to a linear pressure of 100 OkgZcni and a temperature of 100.
- Papermaking was carried out in the same manner as in Example 1 except that the raw material pulp was adjusted to 5F 500 ml by mixing the mixed pulp of 81 1 81 ⁇ with 8 2.
- the paper was 127 g / m 2 , the paper thickness was 168 m, the paper moisture was 5.5%, and the air permeability was 450 sec / 10 Occ.
- This paper was treated under the conditions of a linear pressure of 1500 kg / cm and a temperature of 120 ° C. The thickness of the obtained paper was 95 ni, and the paper habit and curl were slightly bad.
- Example 1 The processing was performed in the same manner as in Example 1 except that the processing conditions were changed to the linear pressure SOOOkgZcn temperature 150 ° C. The thickness of the obtained paper was 96 m. Comparative Example 1
- the raw material pulp was adjusted to 200 ml of CSF with 100% NBKP, and 0.5% rosin-based sizing agent was added to the pulp as an internal sizing agent to make paper.
- a 7% aqueous solution of PVA107 manufactured by Kuraray Co., Ltd. was size-pressed on both sides to a solid content of 2 g / m 2 .
- the obtained paper has a rice tsubo of 70 gZm 2 and an air permeability of 500.
- Example 1 the same processing as in Example 1 was performed except that the processing condition was a linear pressure of 15 OkgZoi.
- the thickness of the obtained paper was 121 / im.
- Example 1 the same processing as in Example 1 was performed except that the processing conditions were a linear pressure of 2800 kgZcin. The resulting paper was partially stretched and no uniform paper was obtained.
- High-pressure treatment was not performed on commercially available high-quality paper with a thickness of 95 m (trade name: medium thickness PPC paper manufactured by Fuji Xerox Office Supply Co., Ltd.).
- a sample with a width of 25.4 rarax and a length of 63.5 mm was measured.
- a weight of 5 g was attached at a position 50.8 mm from the fulcrum of the balanced pendulum. Adjust the position of the test sample grip of the tester to 38.1 mm, and attach the sample to the test sample grip. Grasp the other end of the sample to the position where the specimen is gripped.
- the recoil generated when the specimen was released and the sample returned from the bent state was applied to the balance pendulum of the Gurley, the scale on which the pendulum was swung was read, and the numerical value of the scale was obtained. Measurements were taken in the vertical and horizontal directions of the sample, and the average was taken. A value obtained by multiplying the obtained average value by 100 was defined as a bending return value. The measurement was performed five times for each sample.
- Paper stock was prepared by adding talc, and paper was made with a fourdrinier multi-cylinder paper machine. In the papermaking process, 6.5% liquid (trade name; manufactured by Ace A Oji Cornstarch Co., Ltd.) was subjected to size breathing so that SgZin 2 was obtained by combining both sides with a solid content.
- the obtained paper had a paper moisture of 5.5%, a rice tsubo of 140 g / m 2 and a paper thickness of 175 m.
- This paper was passed through a nip formed by a metal roll and a metal roll at a linear pressure of 1000 kgZcm, a metal roll temperature of 200, and a speed of 5 Om / min.
- the thickness of the obtained paper was 105.
- shellac (trade name manufactured by shellac BN-W25A Gifu Shellac Mills) was coated with a bar coater one such that each 1 OgZin 2.
- a paper was obtained in the same manner as in Example 12, except that the paper made in Example 13 was passed through a nip formed by a metal roll and a metal roll under the conditions of a metal roll temperature of 3 p0 ° C. .
- Example 12 The paper made in Example 12 was passed through a nip formed by a gold roll and a gold roll under the conditions of a linear pressure of 1000 kgZcm, a gold roll temperature of 100 aC, and a speed of 5 5 ⁇ min. ; shellac BN-W25 except that the a manufactured Gifu shellac Mills) was SgZm 2 applied, respectively which give the paper in the same manner as in example 12.
- Paper was obtained in the same manner as in Example 15 except that the amount of the resin applied in Example 15 was changed to 2 Og / m 2 .
- Example 12 to the paper the paper in the example 12 with the paraffin wax on both sides of the paper in which the same high-pressure treatment (trade name: HYDRIN P- 7, Chukyo Yushi Co., Ltd.) to respective concentrations and 10 g Zra? 2 barcode one Coated with tar.
- the same high-pressure treatment (trade name: HYDRIN P- 7, Chukyo Yushi Co., Ltd.) to respective concentrations and 10 g Zra? 2 barcode one Coated with tar.
- Difference m paper (Rule 26) A 10% by weight toluene solution of an aminosilane coupling agent (trade name: KBM 603, manufactured by Shin-Etsu Chemical Co., Ltd.) was prepared, and 10 parts of this solution was dried at 120 ° C for 1 hour, muscovite, average particle size of 20 uni, A drop ratio of 20 to 30 (trade name: Mica A21, manufactured by Mika Yamaguchi Corporation) was added dropwise to 100 parts, and the mixture was stirred at a rotation speed of 100 Orpin for 10 minutes using a mixer, and then dried at 80 ° C for 2 hours.
- an aminosilane coupling agent trade name: KBM 603, manufactured by Shin-Etsu Chemical Co., Ltd.
- Example 12 100 parts of the surface-treated ferrosilicate compound thus treated, 0.2 part of a dispersant (trade name: Kyaribbon L400, manufactured by Toa Gosei Co., Ltd.), 20 parts of 5% by weight ammonia water, and 80 parts of water are mixed. The mixture was dispersed at a rotation speed of 200 Orpin for 30 minutes.
- a ceramic and a glass (trade name: Shellac GN—W25A manufactured by Gifu Shellac Works) were applied on both sides of the paper made in Example 12 with a bar coater to a 9 gm 2 volume, and then coated with a metal roll. It was passed through a nib formed by a metal roll under the conditions of a linear pressure of 1000 kg / cm, a metal roll temperature of 50 ° C, and a speed of 1 1 ⁇ .
- Example 12 The paper made in Example 12 was used.
- Both sides of the paper made in Example 13 were coated with shellac (trade name: Shellac BN-W25A manufactured by Gifu Shellac Mfg. Co., Ltd.) with a bar coater so as to obtain 1 Og / m 2 each to obtain paper.
- shellac trade name: Shellac BN-W25A manufactured by Gifu Shellac Mfg. Co., Ltd.
- Example 12 After the paper making in Example 12, the paper was passed through a metal roll and a nip formed by the metal roll under the conditions of a linear pressure l OOOkg / cm, a metal roll temperature of 350 ° C, and a speed of 2 Om / min. Then, blisters occurred on the surface of the paper, and uniform paper could not be formed.
- Example 12 After the paper making in Example 12, the sheet was passed through a nip formed by a metal roll and a metal roll under the conditions of a linear pressure of 100 Okg / cm, a metal roll temperature of 100 ° C, and a speed of 5 Om / min. Both sides of the obtained paper were coated with shellac (trade name: Shellac BN-W25A manufactured by Gifu Shellac Mfg. Co., Ltd.) with a bar coater to a weight of 2 g / m 2 to obtain paper. (Method of measuring water elongation)
- shellac trade name: Shellac BN-W25A manufactured by Gifu Shellac Mfg. Co., Ltd.
- Table 2 shows the physical properties of the papers obtained in Examples 12 to 19 and Comparative Examples 5 to 8.
- the paper moisture after the coating treatment was 6.0%
- the rice tsubo was 150 g / m 2
- the paper thickness was 194 // in.
- the paper was passed through a nip formed of a metal roll and a metal roll under the conditions of a metal roll temperature of 150 ° C., a linear pressure of 100 OkgZcn and a speed of 2 2 ⁇ . Thereafter, the paper was placed in a hot air drier at 120 ° C. for 30 minutes and cured by heating. The thickness of the obtained paper was 107.
- a coating solution having a concentration of 35% was coated with 9.6 g Zro 2 using a bar coater.
- the paper was passed through a nip formed by a metal roll and a metal roll under the conditions of a metal roll temperature of 150 ° C and a linear pressure of 100 OkgZcn at a speed of 10 ⁇ . Thereafter, the paper was placed in a hot-air dryer for 12 CTC for 30 minutes to be heated and cured.
- the paper thickness of the obtained paper was 110 / m.
- Paper was obtained in the same manner as in Example 20, except that the high-pressure treatment was performed under the conditions of a metal roll temperature of 250, a linear pressure of 500 kg / cm, and a speed of 50 m / min.
- the thickness of the obtained paper was 106 ra.
- Paper was obtained in the same manner as in Example 20, except that the pressure treatment was performed under the conditions of a metal roll temperature of 30 ° C.
- the paper thickness of the obtained paper was 129 / m.
- a paper was obtained in the same manner as in Example 20, except that the resin of Example 21 was used, the resin coating amount was 21.2 g Zni 2 , and the metal roll temperature was 100 ° C. The thickness of the obtained paper was 121 juni.
- a 100% LBKP blended pulp was adjusted to 510 ml of CSF as raw material pulp, and 0.05% of alkenyl succinic anhydride (trade name: Faiburan 81: Arakawa Chemical Co., Ltd.) and cationic powder (trade name: Gate F Oji) 0.7% was added, and talc was added so that the paper ash content became 14% to prepare a stock.
- the stock was made with a fourdrinier multi-cylinder paper machine. In the papermaking process, a 6.5% liquid (trade name; manufactured by Ace Oji Cornstarch Co., Ltd.) was size-pressed to a solid content of 2 gZm 2 on both sides.
- the paper moisture of the paper is 5.5%
- rice tsubo is 262gZm 2
- paper thickness The size was over 100 seconds.
- an initial condensate of urea, glyoxal and formaldehyde [trade name: BECK AMI NE DC-W, manufactured by Kichi Nenki Chemical Industry Co., Ltd .; the molar ratio of urea: glyoxal: formaldehyde is about 1 :: 2.1]
- 100% dipropylene daryl was added and dissolved, and then a catalyst containing magnesium chloride as a main component (trade name: CATALYS TG, manufactured by Dainippon Ink and Chemicals, Inc.) It was coated with a bar coater so that it became 2 .
- the paper moisture after the coating treatment was 6.0%
- the rice tsubo was 287 g / m 2
- the paper thickness was 31 kg.
- the paper was passed through a nip formed by a metal roll and a metal roll under the conditions of a metal roll temperature of 100, a linear pressure of 1000 kgZcm, and a speed of SOmZ. Thereafter, the paper was placed in a hot-air drier for 12 minutes (TC, 60 minutes) and heat-cured.
- the thickness of the obtained paper was 197 mm.
- Example 25 On the paper made in Example 25, an initial condensate of urea, glyoxal and formaldehyde [trade name: BECKAMI NE DC-W manufactured by Dainippon Ink and Chemicals, Inc .; the molar ratio of urea: glyoxal: formaldehyde is about 1: 1: 2.1] 100% polyethylene glycol (average molecular weight: about 600) dissolved in non-volatile components
- Example 25 On the paper made in Example 25, an initial condensate of urea, glyoxal and formaldehyde [trade name: BECKAM I NE DC-W manufactured by Dainippon Ink and Chemicals, Inc .; the molar ratio of urea: glyoxal: formaldehyde was about 1 : 1: 2.1]
- a coating solution prepared by adding 54% of dipropylene glycol to the non-volatile components was applied by a bar coater at 26 g / m 2 . After the coating treatment, the paper moisture was 6.0%, the rice tsubo was 28 SgZiD 2 , and the paper thickness was 313 m.
- the paper was passed through a nip formed by a metal roll and a metal roll under the conditions of a metal roll temperature of 100 ° C. and a linear pressure of 100 ° OkgZcn at a speed of 1.0 minute. Thereafter; the paper was placed in a hot air drier at 190 for 2 hours 30 minutes and heat cured. The thickness of the obtained paper was 200.
- the paper was passed through a metal roll and a nib formed by the metal roll under the conditions of a metal roll temperature of 150, a linear pressure of 1000 kg / cm, and a speed of 1 OmZ. Thereafter, the paper was placed in a hot-air dryer at 120 ° C. for 30 minutes and heat-cured. Basis weight of the resulting paper 157gZia 2, the sheet thickness was 107 m.
- Glyoxal 3% was added to the non-volatile content of the synthesized copolymer, and a 10% aqueous solution of polyacrylic acid (concentration 35%) was added to the non-volatile content of the copolymer and glyoxal to reduce the ion-exchanged water concentration to 10%. %. 100% LBKP pulp as raw material pulp is adjusted to 500ml CSF, 0.3% of mouth gin sizing agent, 1.8% of sulfuric acid band is added to pulp, and talc is added to make paper ash content 16.0% Then, a stock was prepared, and paper was made using a fourdrinier multi-cylinder paper machine.
- the paper moisture after the coating treatment was 6.0%
- the rice tsubo was 157 g / m 2
- the paper thickness was 190 zm.
- Example 20 The paper made in Example 20 was used.
- Example 20 a paper that was not subjected to a heat treatment after passing through a nip formed by a metal roll and a metal roll was used.
- the thickness of this paper was 111 m.
- a paper was obtained in the same manner as in Example 20, except that the resin coat green was changed to 2.4 gZm 2 .
- the thickness of the obtained paper was 109 m.
- Paper was obtained in the same manner as in Example 20, except that the linear pressure was changed to 10 OgZcm. The thickness of the obtained paper was 148 tm.
- Example 20 when the paper was passed with the metal roll temperature set to 350 ° C., a prister occurred.
- Example 23 Before pressure treatment in Example 23, it was placed in a hot air dryer at 120 ° C for 30 minutes, and was heated and cured, and then treated under a pressure treatment condition of a gold-roll temperature of 30 ° C and a linear pressure of 100 OkgZcra. I got the paper. The thickness of the obtained paper was 155 ID.
- Example 25 The paper made in Example 25 was passed only under the conditions of a metal roll temperature of 100 ° C., a linear pressure of 100 Okg / cnu, and a speed of 2 OmZ.
- PEG polyethylene glycol (molecular weight about 600)
- Two sheets of this paper are stacked and passed through the nip formed by a gold roll and a gold roll under the conditions of a linear pressure of 2000 kg / cm, a roll temperature of 200 ° C, and a paper passing speed of 8 OmZ. Lamination was performed to obtain a laminated paper.
- the paper thickness after bonding was 205 / ⁇ , and the paper was bonded without peeling.
- the present invention produced a paper having a high air permeability and a high elasticity with a tension of 1. ZgZcni 3 or more.
- the paper of the present invention also has excellent dimensional stability.
- the paper was not subjected to size press coating.
- the paper exhibited excellent dimensional stability especially at high temperatures and high linear pressures.
- the resin coat weight was changed in Example 12,
- the paper of the present invention has excellent dimensional stability. Without heat treatment, the effect of dimensional stability cannot be obtained. From Example 20 and Comparative Example 10, unless the heat treatment is performed after the pressure treatment, the effect of dimensional stability cannot be obtained. When a heat treatment is performed before the pressure treatment as in Example 23 and Comparative Example 14, although the effect of dimensional stability is obtained, high rigidity and excellent rigidity cannot be obtained. If the linear pressure is lower than that of Comparative Example 12, high tension cannot be obtained. In addition, the addition of glycols increases the permeability of the paper, so that even paper of high size does not remain on the surface.
- ADVANTAGE OF THE INVENTION According to the paper manufacturing method of the present invention in which two or more papers are laminated, only a specific pressure treatment is applied to a nip formed by a metal roll and a metal hole, and a drying step is not required and bonding is performed. Paper can be bonded without using any agent.
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Description
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Priority Applications (1)
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EP96943319A EP0812956A4 (en) | 1995-12-28 | 1996-12-26 | HIGH QUALITY PAPER AND MANUFACTURING METHOD THEREOF |
Applications Claiming Priority (8)
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JP7/344027 | 1995-12-28 | ||
JP34402795 | 1995-12-28 | ||
JP19488296 | 1996-07-24 | ||
JP8/194882 | 1996-07-24 | ||
JP8/219224 | 1996-07-31 | ||
JP21922496 | 1996-07-31 | ||
JP8/265519 | 1996-09-13 | ||
JP26551996 | 1996-09-13 |
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WO1997024489A1 true WO1997024489A1 (fr) | 1997-07-10 |
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PCT/JP1996/003838 WO1997024489A1 (fr) | 1995-12-28 | 1996-12-26 | Papier haute qualite et procede de fabrication correspondant |
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JPH1150388A (ja) * | 1997-08-01 | 1999-02-23 | Oji Paper Co Ltd | 易離解性防湿紙 |
JP2005105153A (ja) * | 2003-09-30 | 2005-04-21 | The Inctec Inc | 接着剤 |
JP2009287159A (ja) * | 2008-04-28 | 2009-12-10 | National Institute Of Agrobiological Sciences | 耐酸耐水性紙シート及びその製造方法 |
CN106894282A (zh) * | 2017-04-18 | 2017-06-27 | 邱雪平 | 一种淋膜纸防水涂料 |
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EP0892109A1 (en) * | 1997-06-27 | 1999-01-20 | Oji Paper Co., Ltd. | A stucture comprising at least one layer containing synthetic fiber |
US6177188B1 (en) * | 1998-03-31 | 2001-01-23 | Canon Kabushiki Kaisha | Recording medium and ink jet recording process using it |
US6528119B1 (en) | 2000-01-18 | 2003-03-04 | Lexmark International, Inc. | Paper coating for ink jet printing |
US6585365B1 (en) | 2000-01-18 | 2003-07-01 | Lexmark International, Inc. | Paper coating for ink jet printing |
AUPQ544900A0 (en) | 2000-02-04 | 2000-02-24 | Commonwealth Scientific And Industrial Research Organisation | Treatment of cellulosic material |
CA2641309A1 (en) | 2006-02-03 | 2007-08-16 | Nanopaper Llc | Functionalization of paper components with an amine-containing polymer |
US7820563B2 (en) | 2006-10-23 | 2010-10-26 | Hawaii Nanosciences, Llc | Compositions and methods for imparting oil repellency and/or water repellency |
EP2079878A2 (en) * | 2006-10-27 | 2009-07-22 | Nanopaper LLC | Pigments for colored paper |
US20080163993A1 (en) * | 2007-01-10 | 2008-07-10 | Varnell Daniel F | Surface sizing with sizing agents and glycol ethers |
US7998311B2 (en) * | 2008-07-24 | 2011-08-16 | Hercules Incorporated | Enhanced surface sizing of paper |
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JPH06266045A (ja) * | 1993-03-12 | 1994-09-22 | Mitsubishi Paper Mills Ltd | 写真用支持体の製造方法 |
-
1996
- 1996-12-26 WO PCT/JP1996/003838 patent/WO1997024489A1/ja not_active Application Discontinuation
- 1996-12-26 EP EP96943319A patent/EP0812956A4/en not_active Withdrawn
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JPH01260094A (ja) * | 1988-04-06 | 1989-10-17 | Kanzaki Paper Mfg Co Ltd | 艶消し塗被紙の製造方法 |
JPH03213598A (ja) * | 1990-01-16 | 1991-09-18 | Oji Paper Co Ltd | オフセット用塗工紙の製造方法 |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH1150388A (ja) * | 1997-08-01 | 1999-02-23 | Oji Paper Co Ltd | 易離解性防湿紙 |
JP2005105153A (ja) * | 2003-09-30 | 2005-04-21 | The Inctec Inc | 接着剤 |
JP2009287159A (ja) * | 2008-04-28 | 2009-12-10 | National Institute Of Agrobiological Sciences | 耐酸耐水性紙シート及びその製造方法 |
CN106894282A (zh) * | 2017-04-18 | 2017-06-27 | 邱雪平 | 一种淋膜纸防水涂料 |
Also Published As
Publication number | Publication date |
---|---|
EP0812956A4 (en) | 2000-05-17 |
EP0812956A1 (en) | 1997-12-17 |
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