EP1835075A1 - Method for making plies for paperboard - Google Patents
Method for making plies for paperboard Download PDFInfo
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- EP1835075A1 EP1835075A1 EP07251134A EP07251134A EP1835075A1 EP 1835075 A1 EP1835075 A1 EP 1835075A1 EP 07251134 A EP07251134 A EP 07251134A EP 07251134 A EP07251134 A EP 07251134A EP 1835075 A1 EP1835075 A1 EP 1835075A1
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- Prior art keywords
- fiber
- paperboard
- slurry
- anionic
- starch
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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
- 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
- D21H23/04—Addition to the pulp; After-treatment of added substances in the pulp
- D21H23/06—Controlling the addition
- D21H23/08—Controlling the addition by measuring pulp properties, e.g. zeta potential, pH
- D21H23/10—Controlling the addition by measuring pulp properties, e.g. zeta potential, pH at least two kinds of compounds being added
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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
- 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
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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
- 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
- D21H23/04—Addition to the pulp; After-treatment of added substances in the pulp
- D21H23/06—Controlling the addition
- D21H23/08—Controlling the addition by measuring pulp properties, e.g. zeta potential, pH
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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
- D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
- D21H11/10—Mixtures of chemical and mechanical pulp
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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
- D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
- D21H11/16—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only modified by a particular after-treatment
- D21H11/20—Chemically or biochemically modified fibres
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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
- 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
- D21H17/28—Starch
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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
- 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
- D21H17/28—Starch
- D21H17/29—Starch cationic
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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
- 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
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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
- 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
- D21H17/54—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
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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
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/63—Inorganic compounds
- D21H17/66—Salts, e.g. alums
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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
- D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
- D21H27/30—Multi-ply
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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
- D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
- D21H27/30—Multi-ply
- D21H27/38—Multi-ply at least one of the sheets having a fibrous composition differing from that of other sheets
Definitions
- This invention relates to methods of making plies for paperboards and to paperboards.
- the application relates to a method for increasing the bond strength in a multi-ply paperboard that has high crosslinked cellulose fiber present in at least one of the plies.
- This application is particularly concerned with a method improving the internal bond strength of paperboard with greater than 25 percent crosslinked fiber in at least one, ply.
- additives are added to the slurry in various combinations and order while maintaining the ionic demand of the slurry at less than zero. Paperboard with high ZDT, Scott Bond and Taber Stiffness is obtained. -
- the invention provides a method for forming at least one ply of a paperboard comprising the steps of forming a slurry of cellulose fibers comprising crosslinked fibers, adding mechanically refined fiber, adding an anionic starch subsequent to adding said mechanically refined fiber, adding a cationic fixative subsequent to adding said anionic starch, wherein, after each addition step, the slurry ionic demand is less than zero, depositing said slurry on a foraminous support, forming a fibrous web layer by withdrawing liquid from said slurry, drying said web to form a paperboard.
- the invention also provides a method for forming a paperboard comprising the steps of forming a slurry of cellulose fibers comprising crosslinked fibers, adding mechanically refined fiber, adding a cationic fixative and mixing with said slurry, adding an anionic starch subsequent to adding said cationic fixative, wherein, after each addition step, the slurry ionic demand is less than zero, depositing said slurry on a foraminous support, forming a fibrous web layer by withdrawing liquid from said slurry, drying said web to form a paperboard.
- the invention further provides a method for forming at least one ply of a paperboard comprising the steps of forming a slurry of cellulose fibers comprising crosslinked fibers, adding mechanically refined fiber, adding an anionic starch subsequent to adding said mechanically refined fiber, adding a first cationic fixative subsequent to adding said anionic starch, adding a second cationic fixative subsequent to adding said first cationic fixative, wherein, after each addition step, the slurry ionic demand is less than zero, depositing said slurry on a foraminous support, forming a fibrous web layer by withdrawing liquid from said slurry, drying said web to form a paperboard.
- the density of the stratum will drop below 0.4 g/cc.
- the internal bond strength can drop so low as to not only be well below levels required for converting the paperboard into packaging products but also below the level where conventional methods of increasing the internal strength cannot provide enough increase to meet minimum levels needed for converting. This effect can occur either in the entire structure or some fraction within the structure.
- the present application provides a method for increasing the internal bond of low density paperboard back into the range which is useable for converting.
- a distinguishing characteristic of the present application is that at least one ply of the paperboard, whether a single-ply or a multiple-ply structure, contains crosslinked cellulose fibers and strength enhancing additives such as mechanically refined fiber, anionic and cationic starches and other additives to offset the board strength lost by adding the crosslinked cellulosic fibers.
- the crosslinked cellulosic fibers increase the bulk density of the insulating paperboard characteristics of the board.
- the paperboard also contains chemical pulp fibers.
- chemical pulp fibers useable in the present application are derived primarily from wood pulp. Suitable wood pulp fibers for use with the application can be obtained from well-known chemical processes such as the kraft and sulfite processes, with or without subsequent bleaching.
- Softwoods and hardwoods can be used. Details of the selection of wood pulp fibers are well known to those skilled in the art. For example, suitable cellulosic fibers produced from southern pine that are useable in the present application are available froma number of companies including Weyerhaeuser Company under the designations C-Pine, Chinook, CF416, FR416, and NB416. A bleached Kraft Douglas Fir pulp (D. Fir), and Grande Prairie Softwood, all manufactured by Weyerhaeuser are examples of northern softwoods that can be used.
- Mercerized fibers such as HPZ and mercerized flash dried fibers such as HPZ III, both manufactured by Buckeye Technologies, Memphis TN, and Porosinier- J-HP available from Rayonier Performance Fibers Division, Jessup, GA are also suitable for use in the present application when used with crosslinked cellulose fibers.
- Non crosslinked cellulose fibers include chemithermomechanical pulp fibers (CTMP), bleached chemithermomechanical pulp fibers (BCTMP), thermomechanical pulp fibers (TMP), refiner groundwood pulp fibers, groundwood pulp fibers, TMP (thermomechanical pulp) made by Weyerhaeuser, Federal Way, WA, and CTMP (chemi-thermomechanical pulp) obtained from NORPAC, Longview, WA, sold as a CTMP NORPAC Newsprint Grade, jet dried cellulosic fibers and treated jet dried cellulosic fibers manufactured by the Weyerhaeuser Company by the method described in U.S. Application No.10/923,447 filed August 20, 2004 . These fibers are twisted kinked and curled. Additional fibers include flash dried and treated flash dried fibers as described in U.S. 6,837,970 ,
- Suitable crosslinking agents for making crosslinked fibers include carboxylic acid crosslinking agents such as polycarboxylic acids.
- carboxylic acid crosslinking agents such as polycarboxylic acids.
- Polycarboxylic acid crosslinking agents e.g., citric acid, propane tricarboxylic acid, and butane tetracarboxylic acid
- catalysts are described in U.S. Patent Nos. 3,526,048 ; 4,820,307 ; 4,936,865 ; 4,975,209 ; and 5,221,285
- C 2 -C 9 polycarboxylic acids that contain at least three carboxyl groups e.g., citric acid and oxydisuccinic acid
- crosslinking agents is described in U.S. Patent Nos. 5,137,537 ; 5,183,707 ; 5,190,563 ; 5,562,740 ; and 5,873,979 .
- Polymeric polycarboxylic acids are also suitable crosslinking agents for making crosslinked fibers. These include polymeric polycarboxylic acid crosslinking agents are described in U.S. Patent Nos. 4,391,878 ; 4,420,368 ; 4,431,481 ; 5,049,235 ; 5,160,789 ; 5,442,899 ; 5,698,074 ; 5,496,476 ; 5,496,477 ; 5,728,771 ; 5,705,475 ; and 5,981,739 . Polyacrylic acid and related copolymers as crosslinking agents are described U.S. Patent Nos. 5,549,791 and 5,998,511 . Polymaleic acid crosslinking agents are described in U.S. Patent No.
- crosslinked cellulosic fibers are present in at least one layer at a level of 25 to 80 percent by total fiber weight of the ply.
- the crosslinked fibers are present at a level of 40 to 75 percent by total fiber weight of the layer and in yet another embodiment they are present at a level of 50 to 70 percent by total fiber weight of the layer.
- the technology relies on the ability to balance the ionic demand in the wet end of the paper machine such that 1) anionic polymeric materials can be retained on the fibers and fines without excess remaining in the water system, 2) the fibers and system do not pass through the zero charge point which destabilizes retention and drainage 3) since pulp fibers are anionic, some cationic material can be added, however, adding too much cationic material without balancing the excess anionic demand will either cause the fibers to flocculate reducing formation and/or cause the drainage to drop, impacting the runnability.
- Each of the components used in the paperboard containing crosslinked fiber in this disclosure has a specific charge density typically measured by ionic demand titration.
- a Mutek PCD-Titrator was used for the particle charge titration coupled with the PCD 02 Particle Charge Detector for measuring the ionic demand of the component or fiber furnish. The method was performed according to a procedure from A.E. Staley Manufacturing, a subsidiary of Tate and Lyle, Decatur, IL The method is as follows.
- Ionic Demand refers to the amount of anionic or cationic charge required to neutralize the counter ion charge and is expressed in meq/g or ueq/kg.
- an additive with an ionic demand of +2.2 meq/g has an anionic demand of 2.2 meq/g; an additive with an ionic demand of -1.8 meq/g has a cationic demand of 1.8 meq/g.
- the difference between the total and available ionic demand represents the amount of charge that is internal to the fiber that is not accessible to polymers of molecular weight above 300,000 g/mole.
- the available ionic demand is more representative of the results obtained in practice than the total ionic demand.
- the fiber slurry is anionic to start with and should remain anionic through the paper making process i.e. the ionic demand of the slurry should less than zero.
- Mechanically refined fiber can be added to the slurry to increase the strength of the paperboard.
- the mechanically refined fiber has a Canadian Standard Freeness of less than 125 mL CSF, a curl index of 1/3 or less of the unrefined fiber and a kink angle of 1/2 or less of the unrefined fiber.
- mechanically refined fiber is added to the slurry followed by the addition of an anionic starch and then followed by addition of a cationic fixative. After each addition step the slurry ionic demand is less than zero.
- the slurry is deposited on a foraminous support, dewatered forming a web and dried to form a paperboard.
- the total starch level on dry fiber is from 50 to 120 lb/t. In another embodiment the total starch level on dry fiber is from 60 to 100 lb/t. In yet another embodiment the total stach level is 80 to 90 lb/t.
- Cationic fixatives such as cationic starch (e.g. STA-LOK® 300, STA-LOK® 330 and RediBOND ®2038) have a low anionic demand i.e. less than 1 meq/g.
- Other cationic additives such as Kymene®557H have a high anionic demand (+2.2 meq/g).
- the cationic fixative has an anionic demand of greater than zero but less than one meq/g.
- the cationic fixative has an anionic demand of from 1 meq/g to 10 meq/g.
- the paperboard of the present application may be one of several structures. In one embodiment the paperboard is a single ply structure, in another the paperboard is a two-ply structure and in yet another embodiment the paperboard is a multi-ply structure.
- the addition order of the additive can vary.
- mechanically refined fiber is added to the slurry followed by the addition of an anionic starch and then followed by addition of a cationic fixative. After each addition step the slurry ionic demand is less than zero.
- the slurry is deposited on a foraminous support, dewatered forming a web and dried to form a paperboard.
- mechanically refined fiber is added to the slurry followed by the addition of a cationic fixative and then followed by addition of an anionic starch. After each addition step the slurry ionic demand is less than zero.
- the slurry is deposited on a foraminous support, dewatered forming a web and dried to form a paperboard.
- mechanically refined fiber is added to the slurry followed by the addition of an anionic starch and then followed by addition of first cationic fixative, followed by adding a second cationic fixative. After each addition step the slurry ionic demand is less than zero.
- the slurry is deposited on a foraminous support, dewatered forming a web and dried to form a paperboard.
- the first cationic fixative may have an anionic demand of from 1 meq/g to 10 meq/g and the second fixant may have an anionic demand of greater than zero but less than 1.
- Fiber and polymer binders were applied to low density board so that internal bond strength increases by 100% or more with 10% or less increase in density.
- the effect of refining on freeness and ionic demand is shown in Table 11.
- mechanically refined fiber is mechanically refined wood pulp for example, Lodgepole Pine having a Canadian Standard Freeness ⁇ 125 mL, a index 1/2 or less of unrefined starting fiber and a kink angle of 1/2 or less of the unrefined starting fiber. Curl Index and kink angle were determined using a Fiber Quality Analyzer (FQA) as published in the Journal of Pulp and Paper Science 21(11):J367 (1995 ). Mechanically refined fiber can be generated to meet these criteria by different refining methods which have different impact on conventional fiber properties. Table III shows the effect on Z-direction tensile and density of various formulations with mechanically refined fiber. ZDT was determined by TAPPI 541.
- Fir 0.256 0.4 80.15 99.3 ⁇ indicates "change in" Internal bond strength can be increased by replacing some of the cationic starch with a higher ionic strength molecule such as Kymene® as shown in the following example. 50% CHB405. 50% Lodgepole Pine refined to 400 mL CSF. 10 #/t Kymene® 557H from Hercules. - 10 #/t Stalok 400 cationic starch from Staley. Mechanically refined Lodgepole pine fiber refined at 50 ml CSF using an Escher Wyss laboratory refiner.
- a third technology is use of a starch excess.
- the general approach was to overcome the normal limits of effective wet-end starch, balancing the charge in the wet-end by adding excess anionic starch and fixing it to the fibers by adding cationic starch or other high charge density cationic polymers thus balancing the system to near neutral charge density.
- the neutralization was important to prevent excessive flocculation and large impacts on drainage.
- total starch content added to the wet can be increased to 2% to 5% based on dry fiber.
- Anionic starch such as RediBOND® 3050 supplied by National Starch & Chemical or Aniofax® AP25 supplied by Carolina Starches can be used.
- Cationic fixatives include common cationic starches like STA-LOK® 300 supplied by Staley Corp., Poly Aluminum Chloride (PAC) like Nalco ULTRION® 8187. or high charge density cationic polymers like M5133 and M5134, GALACTAOL® SP813D (anionic guar) and Kymene® 557H supplied by Hercules Corp. and Nalco NALKAT® 62060 (branched EPEDMA) Nalco NALKAT® 2020 (poly DADMAC).
- a high ionic demand is represented by a polymer that has an ionic demand of 1 meq/g to 17 meq/g, either as an anionic demand or as a cationic demand.
- Kymene®557H has an anionic demand of 2.2 meq/g
- Hercobond®2000 has a cationic demand of 1.8 meq/g.
- the level of anionic starch needed to obtain high strength development depends on the charge density and more importantly on the retention. Typically, 2% to 5% addition level based on dry fiber is adequate.
- the amount of cationic fixative depends entirely on the size of the polymer and the cationic charge density. As defined herein, a fixative is a charged polymer that ionically bonds to a molecule of the opposite charge. In general the higher the charge density the smaller the amount required and for equal charge density the larger the polymer the smaller the amount required.
- control handsheet as described above was adjusted as follows to the non-fiber portion. 40 lbs/t Aniofax AP25 was mixed with the fibers, followed by 20 lbs/t STA-LOK® 300 cationic starch. Kymene® 557H at 5#/t was added and the same combination of Stalok 300 and Aquape1625 as in Example 1, i.e. 20 lb/t and 4 lb/t, respectively. Handsheets were evaluated for density, ZDT and Scott Bond; the results are in Table V 1 combined with the results from Example 1.
- the handsheet formulation described in Example 2 was altered to contain mechanically refined fiber fibers so that the fiber portion of the furnish is:
- Single-ply handsheets designed to simulate the mid-ply of low density multi-ply paperboard were made. A 0.015 percent to 0.035 percent consistency slurry was used in these studies.
- Handsheet making equipment was standard 8" x 8" sheet mold modified with an extended headbox so that twice the normal volume of stock was used. This modification was necessary to improve handsheet formation when using materials designed to generate high bulk (e.g. crosslink fiber such as CHB405 and CHB505). Fiber weights are expressed as a weight percent of the total fiber dry weight; additives are based on weight of dry fiber.
- a series of handsheets were made using different levels of wet-end additives, different addition order and some changes in fiber furnish to demonstrate the level of internal bond strength that could be generated by starch loading the web.
- the additives were added to the slurry in the order across each sample row and the slurry stirred after each addition.
- Table XI shows the conditions and formulations used when making the series of handsheets Table XI-A. Handsheet Formulation And Addition Order. Code Target Basis wt. CHB405 D. Fir PVOH Celanese Celvol 165SF Mechanically Refined Fiber* Anionic Starch Avebe Aniofax AP25 Cationic Starch STA LOK® 300 Anionic Starch Avebe Aniofax AP25 Kymene® 557H Cationic Starch STALOK® 300 Aquapel 650 g/m 2 % % % % #/t #/t #/t #/t #/t #/t 1 250 60% 30% 5% 5% 0 0 0 5 25 4 2 250 60% 35% 0% 5% 0 0 0 5 25 4 2 250 60% 35% 0% 5% 0 0 0 5 25 4 3 250 60% 40% 0% 0% 40 20 0 5 20 4 4 250 60% 35% 0% 5% 40 20 0 5 20 4 5 250 60% 35% 0% 5% 0 20
- Each handsheet was then coated with Polyvinyl Alcohol (PVA) coating, Celvol V24203 supplied by Celanese Ltd.
- PVA Polyvinyl Alcohol
- Celvol V24203 supplied by Celanese Ltd.
- the total coat weight was about 50 g/m 2 and was divided equally between each side of the sheet.
- the coating was added to the surface to facilitate testing Z-direction tensile (ZDT) and internal Scott Bond because low density structures without the coating tend to separate at the tape instead of the within the sheet.
- Samples 1, 2 and 9 can be considered the controls for this experiment.
- Sample number 9 is a fiber formulation designed to deliver low density paper and uses typical wet end chemistry (i.e. cationic starch and Kymene®557H). The result is a very low Scott Bond, but typical Taber Stiffness.
- Sample 2 incorporates mechanically refined fiber in an effort to increase the internal bond and, by itself, results in an increase in ZDT and Scott Bond, but not enough to reach the targets needed for converting multi-ply paperboard. It is estimated the minimum necessary ZDT needed for converting is about 175-190 kPa.
- Sample 1 incorporates mechanically refined fiber with a particle PVOH - known as a good binder but is hindered by issues with retention, cost and process reliability impacts.
- the increase in ZDT and Scott Bond for sample 1 begins to approach the amount needed for converting paperboard.
- Samples 3 and 4 show that by adding 4% total starch to the furnish the ZDT and Scott Bond essentially double. Adding mechanically refined fiber, Sample 4, gives an increase of about the same magnitude as it did to the original structure, Sample 2 v. Sample 4 and Sample 3 v. Sample 9.
- Sample 5 shows reversing the order (i.e. adding cationic starch first then anionic starch) in which the cationic and anionic starch are added makes no difference to the strength development
- Samples 6 and 7 are a case where the amount of anionic starch is doubled while the cationic starch remains constant.
- Kymeme® 557H a higher charge density cationic polymer, is used to balance the additional anionic charge.
- the result is further increase in internal bond, increasing ZDT by 500%, (Sample 6) over the control and Scott Bond is unaffected by the additional starch and Kymene® 557H.
- Sample 7 shows that by adding mechanically refined fiber the effect on ZDT is negative in this case, yet the Scott Bond increases.
- Sample 8 adjusts the source of cationic charge further, increasing the amount of Kymene ®557H and decreasing the amount of cationic starch.
- Table XI-B the ionic demand of the system crosses from negative to positive at the last point of cationic starch addition and from Table XII the corresponding ZDT and Scott bond are further reduced indicating that when the ionic demand exceeds zero the effectiveness of the ionic binding system is reduced.
- Table XIII shows the formulations used in the experiments. Table XIII. Handsheet Formulation and Addition Order Code CHB 405 D.Fir @ 500 ml CSF MRF Anionic Avebe Aniofax® AP25 Cationic STA LOK® 300 Nalco 8187 #/t Nalco 62060 #/t Nalco 2020 #/t Kymene® 557H #/t Cationic STALOK® 300 #/t Wt.
- PVA Polyvinyl Alcohol
- Celvol V24203 supplied by Celanese Ltd.
- the total coat weight was about 50 g/m 2 and was divided equally between each side of the sheet.
- the coating was added to the surface to facilitate testing Z-direction tensile (ZDT) and internal Scott Bond, because low density structures without the coating tend to separate at the tape instead of the within the sheet.
- Sample code 9 from Tables XI and XII above is the base case.
- the fiber furnish used in all of the following examples was the same, only the chemical additives and the order of addition were changed.
- the fiber components were:
- the pilot paper machine was a standard Fourdrinier type single ply former.
- the design is such that there are several chemical addition points so that wet end additive effects can be studied.
- Figure 1 shows the basic unit operations with the chemical addition points. indicated as lower case letters as in Table XV.
- the addition points have been labeled and should be used as a reference for the formulations shown in Table XV.
- Target basis weight was 200 g/m 2 .
- ZDT can be increased by approximately 25% to 85% relative to the same furnish with conventional levels of cationic starch (Codes 2-8, 11-14).
- Starch loading resulted in an increase in density of ⁇ 10% in all cases and had no significant impact on stiffness.
Abstract
Description
- This invention relates to methods of making plies for paperboards and to paperboards. The application relates to a method for increasing the bond strength in a multi-ply paperboard that has high crosslinked cellulose fiber present in at least one of the plies. This application is particularly concerned with a method improving the internal bond strength of paperboard with greater than 25 percent crosslinked fiber in at least one, ply. In the method, additives are added to the slurry in various combinations and order while maintaining the ionic demand of the slurry at less than zero. Paperboard with high ZDT, Scott Bond and Taber Stiffness is obtained. -
- The invention provides a method for forming at least one ply of a paperboard comprising the steps of forming a slurry of cellulose fibers comprising crosslinked fibers, adding mechanically refined fiber, adding an anionic starch subsequent to adding said mechanically refined fiber, adding a cationic fixative subsequent to adding said anionic starch, wherein, after each addition step, the slurry ionic demand is less than zero, depositing said slurry on a foraminous support, forming a fibrous web layer by withdrawing liquid from said slurry, drying said web to form a paperboard.
- The invention also provides a method for forming a paperboard comprising the steps of forming a slurry of cellulose fibers comprising crosslinked fibers, adding mechanically refined fiber, adding a cationic fixative and mixing with said slurry, adding an anionic starch subsequent to adding said cationic fixative, wherein, after each addition step, the slurry ionic demand is less than zero, depositing said slurry on a foraminous support, forming a fibrous web layer by withdrawing liquid from said slurry, drying said web to form a paperboard.
- The invention further provides a method for forming at least one ply of a paperboard comprising the steps of forming a slurry of cellulose fibers comprising crosslinked fibers, adding mechanically refined fiber, adding an anionic starch subsequent to adding said mechanically refined fiber, adding a first cationic fixative subsequent to adding said anionic starch, adding a second cationic fixative subsequent to adding said first cationic fixative, wherein, after each addition step, the slurry ionic demand is less than zero, depositing said slurry on a foraminous support, forming a fibrous web layer by withdrawing liquid from said slurry, drying said web to form a paperboard.
- The following is a description of some specific embodiments of the invention reference being made to Figure which is a schematic diagram of a pilot line for performing the method.
- In single or multi-ply paperboard where the inner plies contain greater than approximately 25 percent crosslinked cellulose fiber the density of the stratum will drop below 0.4 g/cc. As a result, the internal bond strength can drop so low as to not only be well below levels required for converting the paperboard into packaging products but also below the level where conventional methods of increasing the internal strength cannot provide enough increase to meet minimum levels needed for converting. This effect can occur either in the entire structure or some fraction within the structure. The present application provides a method for increasing the internal bond of low density paperboard back into the range which is useable for converting.
- In this application, the use of high concentrations of wet end additives have been demonstrated while producing low density paperboard.
- A distinguishing characteristic of the present application is that at least one ply of the paperboard, whether a single-ply or a multiple-ply structure, contains crosslinked cellulose fibers and strength enhancing additives such as mechanically refined fiber, anionic and cationic starches and other additives to offset the board strength lost by adding the crosslinked cellulosic fibers. The crosslinked cellulosic fibers increase the bulk density of the insulating paperboard characteristics of the board. The paperboard also contains chemical pulp fibers. As defined herein, chemical pulp fibers useable in the present application are derived primarily from wood pulp. Suitable wood pulp fibers for use with the application can be obtained from well-known chemical processes such as the kraft and sulfite processes, with or without subsequent bleaching. Softwoods and hardwoods can be used. Details of the selection of wood pulp fibers are well known to those skilled in the art. For example, suitable cellulosic fibers produced from southern pine that are useable in the present application are available froma number of companies including Weyerhaeuser Company under the designations C-Pine, Chinook, CF416, FR416, and NB416. A bleached Kraft Douglas Fir pulp (D. Fir), and Grande Prairie Softwood, all manufactured by Weyerhaeuser are examples of northern softwoods that can be used. Mercerized fibers such as HPZ and mercerized flash dried fibers such as HPZ III, both manufactured by Buckeye Technologies, Memphis TN, and Porosinier- J-HP available from Rayonier Performance Fibers Division, Jessup, GA are also suitable for use in the present application when used with crosslinked cellulose fibers. Other non crosslinked cellulose fibers include chemithermomechanical pulp fibers (CTMP), bleached chemithermomechanical pulp fibers (BCTMP), thermomechanical pulp fibers (TMP), refiner groundwood pulp fibers, groundwood pulp fibers, TMP (thermomechanical pulp) made by Weyerhaeuser, Federal Way, WA, and CTMP (chemi-thermomechanical pulp) obtained from NORPAC, Longview, WA, sold as a CTMP NORPAC Newsprint Grade, jet dried cellulosic fibers and treated jet dried cellulosic fibers manufactured by the Weyerhaeuser Company by the method described in
U.S. Application No.10/923,447 filed August 20, 2004 U.S. 6,837,970 , - Suitable crosslinking agents for making crosslinked fibers include carboxylic acid crosslinking agents such as polycarboxylic acids. Polycarboxylic acid crosslinking agents (e.g., citric acid, propane tricarboxylic acid, and butane tetracarboxylic acid) and catalysts are described in
U.S. Patent Nos. 3,526,048 ;4,820,307 ;4,936,865 ;4,975,209 ; and5,221,285 The use of C2-C9 polycarboxylic acids that contain at least three carboxyl groups (e.g., citric acid and oxydisuccinic acid) as crosslinking agents is described inU.S. Patent Nos. 5,137,537 ;5,183,707 ;5,190,563 ;5,562,740 ; and5,873,979 . - Polymeric polycarboxylic acids are also suitable crosslinking agents for making crosslinked fibers. These include polymeric polycarboxylic acid crosslinking agents are described in
U.S. Patent Nos. 4,391,878 ;4,420,368 ;4,431,481 ;5,049,235 ;5,160,789 ;5,442,899 ;5,698,074 ;5,496,476 ;5,496,477 ;5,728,771 ;5,705,475 ; and5,981,739 . Polyacrylic acid and related copolymers as crosslinking agents are describedU.S. Patent Nos. 5,549,791 and5,998,511 . Polymaleic acid crosslinking agents are described inU.S. Patent No. 5,998,511 andU.S. 6,582,553 . CHB405, a citric acid crosslinked cellulose fiber and CHB505, a polyacrylic acid crosslinked cellulose, both commercially available from Weyerhaeuser Company, Federal Way, WA were used in this work. - In single or multi-ply paperboard construction a mixture of wood pulp fibers and crosslinked cellulose fibers are used. In one embodiment the crosslinked cellulosic fibers are present in at least one layer at a level of 25 to 80 percent by total fiber weight of the ply. In another embodiment the crosslinked fibers are present at a level of 40 to 75 percent by total fiber weight of the layer and in yet another embodiment they are present at a level of 50 to 70 percent by total fiber weight of the layer.
- The technology relies on the ability to balance the ionic demand in the wet end of the paper machine such that 1) anionic polymeric materials can be retained on the fibers and fines without excess remaining in the water system, 2) the fibers and system do not pass through the zero charge point which destabilizes retention and drainage 3) since pulp fibers are anionic, some cationic material can be added, however, adding too much cationic material without balancing the excess anionic demand will either cause the fibers to flocculate reducing formation and/or cause the drainage to drop, impacting the runnability.
- Each of the components used in the paperboard containing crosslinked fiber in this disclosure has a specific charge density typically measured by ionic demand titration. A Mutek PCD-Titrator was used for the particle charge titration coupled with the PCD 02 Particle Charge Detector for measuring the ionic demand of the component or fiber furnish. The method was performed according to a procedure from A.E. Staley Manufacturing, a subsidiary of Tate and Lyle, Decatur, IL The method is as follows.
- 1. Turn the Mutek on using the power switch on the back of the instrument.
- 2. Place 10 mL of a well mixed sample in the sample vessel. Insert the plunger and washer into the vessel. The sample consistency should be no more than 0.83. Thick stock samples should be diluted.
- 3. With the instrument turned on, the plunger should move up and down and a mV potential should be displayed. The sign of the potential (+ or -) indicates whether the sample is cationic (+) or anionic (-).
- 4. Titrate the sample with the appropriate titrant until the mV potential reads 0 mV (PolyDADMAC is the cationic polymer and is used to titrate anionic samples; PVSK or PESNa are the anionic polymers used to titrate the cationic samples). A buret or syringe can be used to deliver the titrant to the sample. Titration should not be conducted with more than 4 mL of titrant since higher volumes will give inaccurate measurements. If the sample requires more than 4 mL of titrant, the sample should be diluted or more concentrated titrant should be used.
- 5. Record the amount of titrant used to titrate the sample. To calculate the demand of the system, use the following equation:
- Ionic Demand refers to the amount of anionic or cationic charge required to neutralize the counter ion charge and is expressed in meq/g or ueq/kg. For example, an additive with an ionic demand of +2.2 meq/g has an anionic demand of 2.2 meq/g; an additive with an ionic demand of -1.8 meq/g has a cationic demand of 1.8 meq/g.
- Specific components whose ionic demand was measured by the Mutek method are noted in Table 1, other component values are from suppliers.
TABLE I Component Ionic Demand Fully bleached Softwood kraft pulp ~ -0.015 meq/g total Fully bleached Softwood kraft pulp ~ -0.015 meq/g available CHB405 ~ -0.43 meq/g total CHB405 ~ -0.015 meq/g available Kymene® 557H ~ +2.2 meq/g Hercobond® 2000 ~ -1.8 meq/g STA-LOK® 300 ~+0.3 RediBOND® 3050 ~ -0.19 meq/g RediBOND® 2038 ~ +0.24 meq/g STA-LOK® 330 ~+0.41 meq/g PPD M-5133 ~+ 16 meq/g GALACTASOL® SP813D ~ + 2.3 meq/g - With reference to the table, the difference between the total and available ionic demand represents the amount of charge that is internal to the fiber that is not accessible to polymers of molecular weight above 300,000 g/mole. For papermaking, the available ionic demand is more representative of the results obtained in practice than the total ionic demand.
- The situation is further complicated in a paper machine wet-end where dilution water from outside sources and/or wash water from pulp mill bleaching stages contain ionic materials, (both dissolved and dispersed), is used to control consistency of the pulp slurry. In integrated mills where excess ionic materials are present, materials added to the pulp slurry to increase internal bond strength can be consumed by the excess ionic materials. Also, the available ionic sites on pulp will also depend on how much refining has been done and on the basic fiber morphology, i.e. the smaller the fiber or partial fiber the higher available surface area, and therefore the higher available ionic demand.
- In general it may be stated that the fiber slurry is anionic to start with and should remain anionic through the paper making process i.e. the ionic demand of the slurry should less than zero.
- Mechanically refined fiber can be added to the slurry to increase the strength of the paperboard. In one embodiment the mechanically refined fiber has a Canadian Standard Freeness of less than 125 mL CSF, a curl index of 1/3 or less of the unrefined fiber and a kink angle of 1/2 or less of the unrefined fiber.
- In one embodiment mechanically refined fiber is added to the slurry followed by the addition of an anionic starch and then followed by addition of a cationic fixative. After each addition step the slurry ionic demand is less than zero. The slurry is deposited on a foraminous support, dewatered forming a web and dried to form a paperboard.
- In one embodiment the total starch level on dry fiber is from 50 to 120 lb/t. In another embodiment the total starch level on dry fiber is from 60 to 100 lb/t. In yet another embodiment the total stach level is 80 to 90 lb/t.
- Cationic fixatives such as cationic starch (e.g. STA-LOK® 300, STA-LOK® 330 and RediBOND ®2038) have a low anionic demand i.e. less than 1 meq/g. Other cationic additives such as Kymene®557H have a high anionic demand (+2.2 meq/g). In one embodiment the cationic fixative has an anionic demand of greater than zero but less than one meq/g. In another embodiment the cationic fixative has an anionic demand of from 1 meq/g to 10 meq/g.
- The paperboard of the present application may be one of several structures. In one embodiment the paperboard is a single ply structure, in another the paperboard is a two-ply structure and in yet another embodiment the paperboard is a multi-ply structure.
- In the method, the addition order of the additive can vary. As stated earlier, in one embodiment, mechanically refined fiber is added to the slurry followed by the addition of an anionic starch and then followed by addition of a cationic fixative. After each addition step the slurry ionic demand is less than zero. The slurry is deposited on a foraminous support, dewatered forming a web and dried to form a paperboard. In another embodiment mechanically refined fiber is added to the slurry followed by the addition of a cationic fixative and then followed by addition of an anionic starch. After each addition step the slurry ionic demand is less than zero. The slurry is deposited on a foraminous support, dewatered forming a web and dried to form a paperboard. In yet another embodiment, mechanically refined fiber is added to the slurry followed by the addition of an anionic starch and then followed by addition of first cationic fixative, followed by adding a second cationic fixative. After each addition step the slurry ionic demand is less than zero. The slurry is deposited on a foraminous support, dewatered forming a web and dried to form a paperboard. In each case, the first cationic fixative may have an anionic demand of from 1 meq/g to 10 meq/g and the second fixant may have an anionic demand of greater than zero but less than 1.
- Fiber and polymer binders were applied to low density board so that internal bond strength increases by 100% or more with 10% or less increase in density. The effect of refining on freeness and ionic demand is shown in Table 11.
Table II Effect Of Refining On Ionic Demand #Test Fiber Description CSF, mL Curl Index Kink angle, °/mm Ionic Demand,* meq/g 1 LV Lodgepole Pine - Unrefined 720 0.25 92 -0.0008 2 LV Lodgepole Pine - EW 550 0.10 46 -0.0069 3 LV Lodgepole Pine - EW 275 0.07 31 -0.0118 4 LV Doug. Fir - Unrefined 675 0.23 64 5 LV Doug. Fir - EW 85 0.07 28 -0.0114 6 LV Lodgepole Pine - EW 65 0.05 18 -0.0167 7 LV Lodgepole Pine 33 0.05 21 -0.0114 *Fiber only
LV, Longview
EW, Escher Wyss
VB, Valley Beater - 1. Handsheets formed using typical handsheet making equipment with an extension to reduce the forming consistency.
- 2. 250 gsm OD fiber.
- 3. 60% CHB405 (crosslinked fiber), dispersed independently; several methods were used interchangeably (Valley beater with no load, lab disk refiner with 1-2 amps over no load and a pilot scale deflaker. Mechanical dispersion was done to improve formation.
- 4. 40% Douglas Fir refined to 400 ml CSF; pH was adjusted to 7.
- 6. 4 #/t Aquapel sizing agent.
- 7. 5 #/t Kymene®557H.
- 8. 25 #/t cationic starch, (STA-LOK® 300)
The above formulation serves as a control; adjustments to the chemistry are noted in each Example. - As defined herein, mechanically refined fiber (MRF) is mechanically refined wood pulp for example, Lodgepole Pine having a Canadian Standard Freeness <125 mL, a index 1/2 or less of unrefined starting fiber and a kink angle of 1/2 or less of the unrefined starting fiber. Curl Index and kink angle were determined using a Fiber Quality Analyzer (FQA) as published in the Journal of Pulp and Paper Science 21(11):J367 (1995). Mechanically refined fiber can be generated to meet these criteria by different refining methods which have different impact on conventional fiber properties. Table III shows the effect on Z-direction tensile and density of various formulations with mechanically refined fiber. ZDT was determined by TAPPI 541.
Table III Effect Of Mechanically Refined Fiber Addition On Strength Properties Description Density g/cc Change in Density ZDT, kPa Δ ZDT, % 100 % D. Fir 0.628 138 498 1138 Control (as above) 0.264 40.22 10% valley beater mechanically refined fiber replacing 10 % D. Fir 0.292 10.6% 95.38 137 5% Escher Wyss mechanically refined fiber replacing 5 % D. Fir 0.274 3.7% 78.14 94 5% Escher Wyss mechanically refined fiber replacing 5 % D. Fir 0.274 3.7% 110 174 5% Escher Wyss mechanically refined fiber replacing 5 % D. Fir 0.259 -1.9% 52.86 31.4 Control 0.232 24.8 5% Escher Wyss mechanically refined fiber replacing D. Fir 0.238 2.5% 68.95 178 5% mechanically refined fiber replacing D. Fir (double disk refined) 0.242 4.3% 85.5 244 Control 0.255 40.22 5% Valley Beater mechanically refined fiber replacing D. Fir 0.265 3.9 69.81 73.5 Description Density g/cc Change in Density ZDT, kPa Δ ZDT, % 5% Valley Beater mechanically refined fiber replacing D. Fir 0.256 0.4 80.15 99.3 Δ indicates "change in"
Internal bond strength can be increased by replacing some of the cationic starch with a
higher ionic strength molecule such as Kymene® as shown in the following example. 50% CHB405.
50% Lodgepole Pine refined to 400 mL CSF.
10 #/t Kymene® 557H from Hercules. -
10 #/t Stalok 400 cationic starch from Staley.
Mechanically refined Lodgepole pine fiber refined at 50 ml CSF using an Escher Wyss laboratory refiner. - In this formulation the level of the Kymene®557H with an ionic demand of +2.2 meq/g was doubled and the STA-LOK® 300 cationic starch with an ionic demand of + 0.3 meq/g was reduced by 60 %. As noted from the table, significant increases in ZDT bond strength and Scott Bond can be obtained by this method
Table IV Effect On Strength Of Partial Replacement Of Cationic Starch With A Higher Ionic Demand Polymer Mechanically refined fiber % by wt. Density g/cc % Increase ZDT kPa % Increase Scott Bond J/m2 % Increase 0% 0.222 23 98 10% 0.234 +5.4% 62 +170% 135 +38% 20% 0.260 +14.6% 125 +443% 173 +76.5% - A third technology is use of a starch excess. The general approach was to overcome the normal limits of effective wet-end starch, balancing the charge in the wet-end by adding excess anionic starch and fixing it to the fibers by adding cationic starch or other high charge density cationic polymers thus balancing the system to near neutral charge density. The neutralization was important to prevent excessive flocculation and large impacts on drainage. Specifically, total starch content added to the wet can be increased to 2% to 5% based on dry fiber. Anionic starch such as RediBOND® 3050 supplied by National Starch & Chemical or Aniofax® AP25 supplied by Carolina Starches can be used. Cationic fixatives include common cationic starches like STA-LOK® 300 supplied by Staley Corp., Poly Aluminum Chloride (PAC) like Nalco ULTRION® 8187. or high charge density cationic polymers like M5133 and M5134, GALACTAOL® SP813D (anionic guar) and Kymene® 557H supplied by Hercules Corp. and Nalco NALKAT® 62060 (branched EPEDMA) Nalco NALKAT® 2020 (poly DADMAC). As used herein, a high ionic demand is represented by a polymer that has an ionic demand of 1 meq/g to 17 meq/g, either as an anionic demand or as a cationic demand. For example, Kymene®557H has an anionic demand of 2.2 meq/g and Hercobond®2000 has a cationic demand of 1.8 meq/g.
- The level of anionic starch needed to obtain high strength development depends on the charge density and more importantly on the retention. Typically, 2% to 5% addition level based on dry fiber is adequate. The amount of cationic fixative depends entirely on the size of the polymer and the cationic charge density. As defined herein, a fixative is a charged polymer that ionically bonds to a molecule of the opposite charge. In general the higher the charge density the smaller the amount required and for equal charge density the larger the polymer the smaller the amount required.
- The following data was based on laboratory handsheets of the following formulation:
- 1. Handsheets formed using typical handsheet making equipment with an extension to reduce the forming consistency.
- 2. 250 gsm OD fiber.
- 3. 60% CHB405, dispersed independently; several methods were used interchangeably, (Valley Beater with no load, lab disk refiner with 1-2 amps over no load condition, and a pilot scale deflaker). Mechanical dispersion is done to improve formation.
- 4. 40% Douglas Fir refined to 400 ml CSF.
- 5. pH adjusted to 7.
- 6. 5#/t Kymene® 557H.
- 7. 4#/t Aquapel 625 sizing agent.
- 8. 25#/t cationic starch (STA-LOK® 300)
- The above described handsheet is the control. The following adjustments were made to the non-fiber portion of the furnish, 80 lbs/t (4%) Aniofac® AP25 was mixed with the fibers, followed by 20 lbs/t cationic starch STA-LOK® 300. Then Kymene®557H was added and the amount increased to 10 lbs/t. Last, before sheet making a blend of cationic starch STA-LOK® 300 and Aquapel 625 were added, the cationic starch was reduced to 20 lbs/t and the Aquapel was kept constant at 4 lbs/t. Handsheets were evaluated for density, ZDT and Scott Bond the results are in Table V.
Table V Description Density g/cc ZDT kPa Scott Bond J/m2 Control 0.243 45 80 4% Anionic Starch (Aniofac® AP25) Example 1 0.273 204 119 - The control handsheet as described above was adjusted as follows to the non-fiber portion. 40 lbs/t Aniofax AP25 was mixed with the fibers, followed by 20 lbs/t STA-LOK® 300 cationic starch. Kymene® 557H at 5#/t was added and the same combination of Stalok 300 and Aquape1625 as in Example 1, i.e. 20 lb/t and 4 lb/t, respectively. Handsheets were evaluated for density, ZDT and Scott Bond; the results are in Table V 1 combined with the results from Example 1.
Table VI Description Density g/cc ZDT kPa Scott Bond J/m2 Control 0.243 45 80 4% Anionic Starch* Example 1 0.273 204 119 2% Anionic Starch* Example 2 0.262 85 113 *Aniofac® AP25 - The handsheet formulation described in Example 2 was altered to contain mechanically refined fiber fibers so that the fiber portion of the furnish is:
- 60% CHB405.
- 35% Fully Bleached D. Fir refined to 400 mL CSF.
- 5% Valley beater mechanically refined fiber - fully bleached kraft Lodgepole Pine at -50 mL CSF.
- Adjustments were made to the non-fiber portion of the of the handsheet formulation described in Example 3 (containing mechanically refined fiber) as follows:
- 100 lb/t Aniofax® AP25 (was blended with the fibers followed by 90 lb/t Nalco 8187 PAC, then 5 lb/
t Kymene® 557H, 5 lb/t STA-LOK® 300 and 4 lb/t Aquapel 625. The results are shown in Table VIII. - Adjustments were made to the non-fiber portion of the of the handsheet formulation described in Example 3 (containing mechanically refined fiber) as follows: 50 lb/t Aniofax® AP25 was blended with the fibers followed by 8 lb/t Nalco 62060 poly, then 5 lb/
t Kymene® 557H, 5 lb/t STA-LOK® 300 and 4 lb/t Aquapel 625. The results are shown in the Table IX.Table IX Description Density g/cc ZDT kPa Scott Bond J/m2 Control 0.243 45 80 Control + 5% Mechanically refined fiber 0.274 78 106 5% Anionic starch* + 4.5% PAC Example 4 0.304 142 214 2.5% Anionic starch* + 0.4% Poly DADMAC Example 5 0.284 109 138 *Aniofac® AP25 - Adjustments were made to the non-fiber portion of the of the handsheet formulation described in Example 3 (containing mechanically refined fiber) as follows:100 lb/t Aniofax® AP25 was blended with the fibers followed by 6 lb/t Nalco 2020 poly, then 5 lb/
t Kymene® 557H, 5 lb/t STA-LOK® 300 and 4 lb/t Aquapel 625. The results are shown in Table X.Table X Description Density g/cc ZDT kPa Scott Bond J/m2 Control 0.243 45 80 Control + 5% Mechanically refined fiber 0.274 78 106 5% Anionic starch* + 4.5% PAC Example 4 0.304 142 214 2.5% Anionic starch* + 0.4% Poly DADMAC Example 5 0.284 109 138 5% Anionic Starch* + 0.3% Poly Example 6 0.279 218 215 *Aniofac® AP25 - Single-ply handsheets designed to simulate the mid-ply of low density multi-ply paperboard were made. A 0.015 percent to 0.035 percent consistency slurry was used in these studies. Handsheet making equipment was standard 8" x 8" sheet mold modified with an extended headbox so that twice the normal volume of stock was used. This modification was necessary to improve handsheet formation when using materials designed to generate high bulk (e.g. crosslink fiber such as CHB405 and CHB505). Fiber weights are expressed as a weight percent of the total fiber dry weight; additives are based on weight of dry fiber.
- A series of handsheets were made using different levels of wet-end additives, different addition order and some changes in fiber furnish to demonstrate the level of internal bond strength that could be generated by starch loading the web. The additives were added to the slurry in the order across each sample row and the slurry stirred after each addition.
- The Table XI below shows the conditions and formulations used when making the series of handsheets
Table XI-A. Handsheet Formulation And Addition Order. Code Target Basis wt. CHB405 D. Fir PVOH Celanese Celvol 165SF Mechanically Refined Fiber* Anionic Starch Avebe Aniofax AP25 Cationic Starch STA LOK® 300 Anionic Starch Avebe Aniofax AP25 Kymene® 557H Cationic Starch STALOK® 300 Aquapel 650 g/m2 % % % % #/t #/t #/t #/t #/t #/t 1 250 60% 30% 5% 5% 0 0 0 5 25 4 2 250 60% 35% 0% 5% 0 0 0 5 25 4 3 250 60% 40% 0% 0% 40 20 0 5 20 4 4 250 60% 35% 0% 5% 40 20 0 5 20 4 5 250 60% 35% 0% 5% 0 20 40 5 20 4 6 250 60% 35% 0% 0% 80 20 0 10 10 4 7 250 60% 35% 0% 5% 80 20 0 10 10 4 8 250 60% 35% 0% 5% 0 10 80 15 10 4 9 250 60% 40% 0% 0% 0 0 0 5 25 4 * Lodgepole Pine refined with Valley Beater to 33 CSF Table XI-B. Calculated Ionic Demand As Chemical Additions Are Made In Table XI-A Code Ionic demand CHB405 Ionic demand D. Fir Ionic demand PVOH Ionic demand MRF Ionic demand, total pulp and particles Ionic strength with Aniofax® AP25 Ionic strength with STALOK® 300 Ionic strength with Aniofax® AP25 Ionic strength with Kymene® 557H Ionic strength with STA LOK® 300 Ionic strength with Aquapel 650 - end point ueq/g ueq/g ueq/g ueq/g ueq/g ueq/g ueq/g ueq/g ueq/g ueq/g ueq/g 1 -9 -0.45 0 -0.57 -10.02 -10.02 -10.02 -10.02 -4.52 -0.89 -0.89 2 -9 -0.53 0 -0.57 -10.1 -10.1 -10.1 -10.1 -4.60 -0.97 -0.97 3 -9 -0.6 0 0 -0.96 -14.2 -11.3 -11.3 -5.8 -2.9 -2.9 4 -9 -0.53 0 -0.57 -10.1 -14.7 -11.8 -11.8 -6.3 -3.40 -3.40 5 -9 -0.53 0 -0.57 -10.1 -10.1 -7.20 -11.8 -6.3 -3.40 -3.40 6 -9 -0.53 0 0 -9.53 -18.7 -15.8 -15.8 -4.8 -3.38 -3.38 7 -9 -0.53 0 -0.57 -10.1 -19.3 -16.4 -16.4 -5.4 -3.94 -3.94 8 -9 -0.53 0 -0.57 -10.1 -10.1 -0.86 -0.86 -1.34 0.11 0.11 9 -9 -0.6 0 0 -0.96 -0.96 -0.96 -0.96 -4.1 -0.48 -0.48 - Each handsheet was then coated with Polyvinyl Alcohol (PVA) coating, Celvol V24203 supplied by Celanese Ltd. The total coat weight was about 50 g/m2 and was divided equally between each side of the sheet. The coating was added to the surface to facilitate testing Z-direction tensile (ZDT) and internal Scott Bond because low density structures without the coating tend to separate at the tape instead of the within the sheet.
- Each sheet was evaluated for several physical properties including basis weight, caliper, ZDT, internal Scott Bond and Taber Stiffness (15°). Scott Bond and Taber Stiffness were determined by TAPPI T 569 om-00 and T 489 om-04, respectively. Table XII below shows the results for these key characteristics
Table XII. Physical Characteristics of Laboratory Handsheets as Described in Table XI Sample Basis Weight Density Z-direction Tensile Scott Bond Taber Stiffness g/m2 g/cm3 kPa J/m2 g cm 1 297 0.267 124 158 375 2 296 0.274 78 106 316 3 306 0.262 85 113 433 4 303 0.283 122 147 387 5 303 0.281 121 142 388 6 305 0.273 204 119 403 7 301 0.284 179 128 374 8 303 0.284 140 116 394 9 301 0.264 40 67 364 -
Samples Sample number 9 is a fiber formulation designed to deliver low density paper and uses typical wet end chemistry (i.e. cationic starch and Kymene®557H). The result is a very low Scott Bond, but typical Taber Stiffness.Sample 2, incorporates mechanically refined fiber in an effort to increase the internal bond and, by itself, results in an increase in ZDT and Scott Bond, but not enough to reach the targets needed for converting multi-ply paperboard. It is estimated the minimum necessary ZDT needed for converting is about 175-190 kPa. - Sample 1 incorporates mechanically refined fiber with a particle PVOH - known as a good binder but is hindered by issues with retention, cost and process reliability impacts. The increase in ZDT and Scott Bond for sample 1 begins to approach the amount needed for converting paperboard. Samples 3 and 4 show that by adding 4% total starch to the furnish the ZDT and Scott Bond essentially double. Adding mechanically refined fiber, Sample 4, gives an increase of about the same magnitude as it did to the original structure,
Sample 2 v. Sample 4 and Sample 3 v.Sample 9. -
Sample 5 shows reversing the order (i.e. adding cationic starch first then anionic starch) in which the cationic and anionic starch are added makes no difference to the strength development -
Samples 6 and 7 are a case where the amount of anionic starch is doubled while the cationic starch remains constant. Kymeme® 557H, a higher charge density cationic polymer, is used to balance the additional anionic charge. The result is further increase in internal bond, increasing ZDT by 500%, (Sample 6) over the control and Scott Bond is unaffected by the additional starch and Kymene® 557H.Sample 7 shows that by adding mechanically refined fiber the effect on ZDT is negative in this case, yet the Scott Bond increases. -
Sample 8 adjusts the source of cationic charge further, increasing the amount of Kymene ®557H and decreasing the amount of cationic starch. In Table XI-B the ionic demand of the system crosses from negative to positive at the last point of cationic starch addition and from Table XII the corresponding ZDT and Scott bond are further reduced indicating that when the ionic demand exceeds zero the effectiveness of the ionic binding system is reduced. - The ZDT is reduced further, indicating that higher charge density polymer is less effective than cationic starch in adding internal bond strength. In general the impact of the starch loading on Taber Stiffness at 15° is small. For single ply handsheets this is reasonable because caliper is the dominating variable effecting bending stiffness. The impact of the starch loading on density is small enough that the increase in elastic modulus of the sheets due to the starch loading compensates for the small changes in caliper. In a multi-ply web the same response would be expected.
- A second set of handsheets was produced to determine the impact of using high charge density cationic polymers to retain additional anionic starch. It is thought that using higher charge density polymers less total starch would be necessary to achieve the same strength due to better retention. The result would reduce the risk of affecting drainage and formation by adding excess starch. Table XIII shows the formulations used in the experiments.
Table XIII. Handsheet Formulation and Addition Order Code CHB 405 D.Fir @ 500 ml CSF MRF Anionic Avebe Aniofax® AP25 Cationic STA LOK® 300 Nalco 8187 #/t Nalco 62060 #/t Nalco 2020 #/t Kymene® 557H #/t Cationic STALOK® 300 #/t Wt. % Wt. % Wt. % #/t #/t 1 60 35 5 80 20 5 5 2 60 35 5 50 25 5 5 3 60 35 5 50 40 5 5 4 60 35 5 100 60 5 5 5 60 35 5 100 90 5 5 6 60 35 5 50 4 5 5 7 60 35 5 50 8 5 5 8 60 35 5 100 6 5 5 9 60 35 5 100 12 5 5 10 60 35 5 50 4 5 5 11 60 35 5 50 8 5 5 12 60 35 5 100 6 5 13 60 35 5 100 12 5 5 14 0 100 0 5 25 All Codes at 250 g/m2 target; all additives are on a dry fiber wt. basis
Aquapel 650 at 4 #/ton was used in all the studies (dry fiber weight basis)
MRF: Mechanically refined Fiber - Each handsheet was then coated with Polyvinyl Alcohol (PVA) coating, Celvol V24203 supplied by Celanese Ltd. The total coat weight was about 50 g/m2 and was divided equally between each side of the sheet. The coating was added to the surface to facilitate testing Z-direction tensile (ZDT) and internal Scott Bond, because low density structures without the coating tend to separate at the tape instead of the within the sheet.
- Each sheet was evaluated for several physical properties including basis weight, caliper, ZDT, Internal Scott Bond, Taber Stiffness (15°) and other. The table below shows the results for these key characteristics
Table XIV. Physical Characteristics Of Laboratory Handsheets As Described In Table XIII Code Basis Weight Density Z-direction Tensile Scott Bond Taber Stiffness g/m2 g/cm3 kPa J/m2 g cm 1 306 0.287 186 132 392 2 317 0.285 107 137 408 3 314 0.278 83 130 394 4 311 0.287 118 164 388 5 320 0.304 142 214 400 6 303 0.286 87 122 373 7 309 0.284 109 138 392 8 304 0.272 107 104 380 9 306 0.276 118 141 389 10 305 0.281 100 112 384 11 308 0.282 103 141 394 12 308 0.279 218 215 390 13 307 0.276 122 109 394 14 270 0.628 498 329 116 From Table XII - control with normal strength additives, as a reference. 9 301 0.264 40 67 364 -
Sample code 9 from Tables XI and XII above is the base case. - The impact of using PAC such as Nalco 8187 (codes 2-5) to retain the anionic starch in the presence of mechanically refined fiber is less than that of using cationic starch on ZDT, however the impact on Scott Bond is greater, suggesting that the PAC improves the retention of the mechanically refined fiber giving greater shear strength to the board.
- For codes 6-9 using NALKAT®62060 a branched EPEDMA cationic polymer as a fixative, the impact at 2.5% anionic starch addition is roughly the same as the PAC Nalco 8187) but significantly less ZDT development relative to the cationic starch, Code 1. At the 5% anionic starch addition level there was no further significant gain
- Use of the polyDADMAC (codes 10-13) as a fixative shows more promise than the other two cationic polymers at the 5% added starch dose where it exceeded (Code 12) the cationic starch in ZDT and Scott Bond development vs Code 1
- The last code in Tables XIII and XIV,
Code 14, is that of a normal density board, included for comparison. The higher ZDT and Scott Bond come at the expense of bending stiffness. - In general, at equal total starch levels it appears that more ZDT is developed when using combination of anionic and cationic starch than when using higher charge density cationic polymers in combination with anionic starch. However, both methods develop significant ZDT. Scott Bond has the opposite result. The shear strength appears to increase at a greater rate than the ZDT when using higher charge density cationic polymers in combination with anionic starch.
- Finally, the impact of the starch loading, independent of the cationic fixative has little effect on the product density and therefore little impact on the bending stiffness.
- The disclosure was further explored using a pilot paper machine where dynamic drainage and white water re-circulation could be used to improve the simulation of commercial application on a paper machine.
- The fiber furnish used in all of the following examples was the same, only the chemical additives and the order of addition were changed. The fiber components were:
- 60% Weyerhaeuser CHB405
- 35% Weyerhaeuser fully bleached kraft D. Fir wet lap refined to ~500 mL CSF
- 5% Douglas Fir refined to 85 ml CSF (Escher Wyss refined)
- The chemical components were combinations of some or all of the following, levels and addition order are shown in Table XV.
Kymene® 557H supplied by Hercules Incorporated (cationic wet strength resin) Aquapel® 650 supplied by Hercules Incorporated (AKD sizing agent)
Hercobond® 2000 supplied by Hercules Incorporated (anionic polyacrylamide, retention aid)
RediBOND® 3050 supplied by Hercules Incorporated (anionic starch)
RediBOND® 2038 supplied by Hercules Incorporated (cationic starch)
PPD M-5133 supplied by Hercules Incorporated (cationic high charge density polymer)
GALACTASOL® SP813D supplied by Hercules Incorporated (cationic guar gum) - The pilot paper machine was a standard Fourdrinier type single ply former. The design is such that there are several chemical addition points so that wet end additive effects can be studied. Figure 1 shows the basic unit operations with the chemical addition points. indicated as lower case letters as in Table XV. The addition points have been labeled and should be used as a reference for the formulations shown in Table XV.
- Other unit operations were changed to maximize the bulk, for example, lowering the amount of vacuum on the forming table suction boxes, lifting the Dandy rolls away from the web using only one wet press, a normal drying profile, no size press (typical solids entering dryer 32-36%) no calendaring and finally, samples were taken for evaluation at the reel (eliminating effect of reel tension)
- For each different formulation, the machine was run 10 to 15 minutes after making adjustments and insuring the basis weight was on target. In this way, the white water was completely turned over and reach equilibrium with the new chemistry. Target basis weight was 200 g/m2.
- Each sample was then coated with Polyvinyl Alcohol (PVA) coating, Celvol V24203 supplied by Celanese Ltd. The total coat weight was about 22 g/m2 and was divided equally between each side of the sheet. The coating was added to the surface to facilitate testing Z-direction tensile (ZDT) and Internal Scott Bond, because low density structures without the coating tend to separate at the tape instead of the within the sheet.
Table XV. Wet End Additives for Pilot Paper Machine Starch Loading Trials. Code b c d e g h 1 5 #/t Kymene® 557H 2 #/t Hercobond 2000 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 2 20 #/t RediBond2038 20 #/t RediBOND 3050 5 #/t Kymene ® 557H 2 #/t Hercobond 2000 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 3 20 #/t RediBond 2038 20 #/t RediBOND 3050 5 #/t Kymene® 557H 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 4 30 #/t RediBond 2038 40 #/t RediBOND 3050 5 #/t Kymene® 557H 2 #/t Hercobond 2000 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 5 20 #/t RediBond 2038 60 #/t RediBOND 3050 10 #/t Kymene® 557H 2 #/t Hercobond 2000 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 6 20 #/t RediBond 2038 10 #/t Kymene ®557H 20 #/t RediBOND 3050 2 #/t Hercobond 2000 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 7 30 #/t RediBond 2038 10 #/t Kymene® 557H 40 #/t RediBOND 3050 2 #/t Hercobond 2000 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 8 40 #/t RediBond 2038 20 #/t RediBOND 2038 5 #/t Kymene® 557H 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 9 40 #/t RediBOND 3050 2 #/t M-5133 8.2 #/t Hercobond 2000 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 10 5 #/t Kymene® 557H 2 #/t Hercobond 2000 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 11 30 #/t RediBOND 2038 10 #/t Kymene® 557H 40 #/t RediBOND 3050 2 #/t Hercobond 2000 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 12 30 #/t RediBOND 2038 5 #/t Kymene® 557H 40 #/t RediBOND 3050 2 #/t Hercobond 2000 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 13 30 #/t RediBOND 2038 2.5 #/t Kymene® 557H 40 #/t RediBOND 3050 2 #/t Hercobond 2000 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 14 30 #/t RediBOND 2038 40 #/t RediBOND 3050 5 #/t Kymene® 557H 2 #/t Hercobond 2000 10 #/t RediBOND 2038 4.5 #/t Aquapel 650 15 8 #/t GALACTASOL SP813D 40 #/t RediBOND 3050 5 #/t Kymene® 557H 2 #/t Hercobond 2000 8 #/t GALACTASOL SP813D 4.5 #/t Aquapel 650 16 40 #/t RediBOND 3050 20 #/t RediBOND 2038 5 #/t Kymene® 557H 4 #/t GALACTASOL SP813D 4.5 #/t Aquapel 650 Lower case letters refer to the additive addition points in Figure 1 Table XVI. Physical Characteristics of Pilot Paper Machine Samples in Table XV Code Basis Weight Density Z-direction Tensile Geometric Mean Scott Bond Geometric Mean Taber Stiffness g/m2 g/cm3 kPa J/m2 g cm 1 228 0.271 161 198 _135 2 256 0.273 194 242 163 3 251 0.283 204 258 161 4 245 0.274 219 252 166 5 237 0.284 265 236 147 6 236 0.276 241 227 146 7 239 0.279 232 236 146 8 262 0.288 199 246 190 9 236 0.260 134 189 156 10 231 0.271 192 227 140 11 230 0.295 350 354 127 12 229 0.290 360 340 131 13 234 0.288 319 323 131 14 244 0.292 339 340 144 15 228 0.288 305 297 134 16 243 0.273 269 345 146 - The effect of starch loading is basically the same, it is estimated that the target internal bond strength that would be enough for performance during converting is about 2x of the control samples. For the pilot trial ZDT doubled and Scott Bond increased 75 %.
- By loading the wet-end with between 2% and 4% total starch (anionic and cationic), ZDT can be increased by approximately 25% to 85% relative to the same furnish with conventional levels of cationic starch (Codes 2-8, 11-14).
- Loading up to 2% anionic starch into the wet-end and using high charge density cationic polymer (code 9) to retain the starch little or no gain in ZDT or Scott Bond was achieved.
- Loading the wet-end with up to 2% anionic starch and using cationic guar gum (
codes 15 and 16) to improve retention as a substitute for cationic starch about 40%-50% increase in ZDT was obtained. - When changing the order of addition, indications were that adding the anionic starch after the cationic material resulted in better strength efficiency.
- Starch loading resulted in an increase in density of < 10% in all cases and had no significant impact on stiffness.
Description | Density g/cc | ZDT kPa | Scott Bond J/m2 | |
Control | 0.243 | 45 | 80 | |
4% Anionic Starch* | Example 1 | 0.273 | 204 | 119 |
2% Anionic Starch* | Example 2 | 0.262 | 85 | 113 |
Control + 5% Mechanically refined fiber | 0.274 | 78 | 106 | |
2% anionic starch + 5% mechanically refined fiber | Example 3 | 0.283 | 122 | 148 |
*Aniofac® AP25 |
Description | Density g/cc | ZDT kPa | Scott Bond J/m2 | |
Control | 0.243 | 45 | 80 | |
Control + 5% mechanically refined fiber | 0.274 | 78 | 106 | |
5% Anionic starch*+4.5% PAC | Example 4 | 0.304 | 142 | 214 |
*Aniofac® AP25 |
Claims (24)
- A method for forming at least one ply of a paperboard comprising the steps of:forming a slurry of cellulose fibers comprising crosslinked fibers;adding mechanically refined fiber;adding an anionic starch subsequent to adding said mechanically refined fiber;adding a cationic fixative subsequent to adding said anionic starch;wherein, after each addition step, the slurry ionic demand is less than zero;depositing said slurry on a foraminous support;forming a fibrous web layer by withdrawing liquid from said slurry;drying said web to form a paperboard.
- A method as claimed in Claim 1, wherein said crosslinked fibers are present at a level from 25 to 80 percent of the total fiber weight in at least one ply of said paperboard.
- A method as claimed in Claim 1 or Claim 2, wherein the total starch level is 50 to 120 lb/t.
- A method as claimed in any of Claims 1 to 3, wherein the mechanically refined fiber has a CSF of less than 125 CSF, a curl index of 1/3 or less of the unrefined fiber and a kink angle of ½ or less of the unrefined fiber.
- A method as claimed in any of Claims 1 to 4, wherein the cationic fixative has an anionic demand of greater than zero but less than 1 meq/g.
- A method as claimed in any of Claims 1 to 4, wherein the cationic fixative has an anionic demand of from 1 meq/g to 10 meq/g.
- A method as claimed in any of Claims 1 to 6, wherein said paperboard is at least a two-ply board, said at least one ply containing said crosslinked fibers.
- A method as claimed in any of Claims 1 to 6, wherein said paperboard is at least a three-ply board, said at least one ply containing said crosslinked fibers.
- A method for forming a paperboard comprising the steps of:forming a slurry of cellulose fibers comprising crosslinked fibers;adding mechanically refined fiber,adding a cationic fixative and mixing with said slurry;adding an anionic starch subsequent to adding said cationic fixative;wherein, after each addition step, the slurry ionic demand is less than zero;depositing said slurry on a foraminous support;forming a fibrous web layer by withdrawing liquid from said slurry;drying said web to form a paperboard.
- A method as claimed in Claim 9, wherein said crosslinked fibers are present at a level from 25 to 80 percent of the total fiber weight in at least one ply of said paperboard.
- A method as claimed in any of Claim 9 or Claim 10, wherein the total starch level is 50 to 120 lb/t.
- A method as claimed in any of Claims 9 to 11, wherein the mechanically refined fiber has a CSF of less than 125 CSF, a index of 1/3 or less of the unrefined fiber and a kink angle of 1/2 or less of the unrefined fiber.
- A method as claimed in any of Claims 9 to 12, wherein the cationic fixative has an anionic demand of greater than zero but less than 1 meq/g.
- A method as claimed in any of Claims 9 to 12, wherein the cationic fixative has an anionic demand of from 1 meq/g to about 10 meq/g.
- A method as claimed in any of Claims 9 to 14, wherein said paperboard is at least a two-ply board, said at least one ply containing said crosslinked fibers.
- A method as claimed in any of Claims 9 to 14, wherein said paperboard is at least a three-ply board, said at least one ply containing said crosslinked fibers.
- A method for forming at least one ply of a paperboard comprising the steps of:forming a slurry of cellulose fibers comprising crosslinked fibers;adding mechanically refined fiber;adding an anionic starch subsequent to adding said mechanically refined fiber;adding a first cationic fixative subsequent to adding said anionic starch;adding a second cationic fixative subsequent to adding said first cationic fixative;wherein, after each addition step, the slurry ionic demand is less than zero;depositing said slurry on a foraminous support;forming a fibrous web layer by withdrawing liquid from said slurry;drying said web to form a paperboard.
- A method as claimed in Claim 17, wherein said crosslinked fibers are present at a level from 25 to 80 percent of the total fiber weight in at least one ply of said paperboard.
- A method as claimed in Claim 17 or Claim 18, wherein the total starch level is 50 to 120 lb/t.
- A method as claimed in any of Claims 17 to 19, wherein the mechanically refined fiber has a CSF of less than 125 CSF, a curl index of 1/3 or less of the unrefined fiber and a kink angle of 1/2 or less of the unrefined fiber.
- A method as claimed in any of Claims 17 to 20, wherein the first cationic fixative has an anionic demand of from 1 meq/g to 10 meq/g.
- A method as claimed in any of Claim 17 to 20, wherein the second cationic fixative has an anionic demand of greater than zero but less than 1 meq/g.
- A method as claimed in any of Claim 17 to 22, wherein said paperboard is at least a two-ply board, said at least one ply containing said crosslinked fibers.
- A method as claimed in any of Claims 17 to 22, wherein said paperboard is at least a three-ply board, said at least one ply containing said crosslinked fibers.
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US (1) | US20070215301A1 (en) |
EP (1) | EP1835075A1 (en) |
JP (1) | JP2007254948A (en) |
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WO2012039668A1 (en) * | 2010-09-22 | 2012-03-29 | Stora Enso Oyj | A paper or paperboard product and a process for production of a paper or paperboard product |
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WO2017065800A1 (en) * | 2015-10-16 | 2017-04-20 | General Mills, Inc. | Paperboard product |
WO2017147392A1 (en) | 2016-02-26 | 2017-08-31 | Ecolab Usa Inc. | Drainage management in multi-ply papermaking |
US10415188B1 (en) * | 2016-06-28 | 2019-09-17 | Gpcp Ip Holdings Llc | Disposable cups made form recycled fiber |
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