Classifications

• • D—TEXTILES; PAPER
  • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
  • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
  • 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
  • D21H21/06—Paper forming aids
  • D21H21/10—Retention agents or drainage improvers
• • 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
• • 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
  • D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • D21H17/41—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
  • D21H17/42—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups anionic
• • D—TEXTILES; PAPER
  • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
  • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
  • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
  • D21H17/20—Macromolecular organic compounds
  • D21H17/33—Synthetic macromolecular compounds
  • D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • D21H17/41—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
  • D21H17/44—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups cationic
• • D—TEXTILES; PAPER
  • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
  • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
  • 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
  • D21H17/55—Polyamides; Polyaminoamides; Polyester-amides

Definitions

• This invention relates to the process of making paper and paperboard from a cellulosic stock, employing a flocculating system.
• the making of cellulosic fiber sheets includes the following: 1) producing an aqueous slurry of cellulosic fiber which may also contain inorganic mineral extenders or pigments; 2) depositing this slurry on a moving papermaking wire or fabric; and 3) forming a sheet from the solid components of the slurry by draining the water.
• Drainage or dewatering of the fibrous slurry on the papermaking wire or fabric is often the limiting step in achieving faster paper machine speeds. Improved dewatering can also result in a drier sheet in the press and dryer sections, resulting in reduced energy consumption.
• the retention and/or drainage aid can impact performance attributes of the final paper sheet.
• papermaking retention aids are used to increase the retention of fine furnish solids in the web during the turbulent method of draining and forming the paper web. Without adequate retention of the fine solids, they are either lost to the mill effluent or accumulate to high levels in the recirculating white water loop, potentially causing deposit buildup. Additionally, insufficient retention increases the papermakers' cost due to loss of additives intended to be adsorbed on the fiber. Additives can provide opacity, strength, sizing or other desirable properties to the paper.
• a method of improving retention and drainage in a papermaking process is disclosed.
• the method provides for the addition of an associative polymer and an organic microparticle to a papermaking slurry.
• composition comprising an associative polymer and an organic microparticle and optionally further comprising cellulose fiber is disclosed.
• composition comprising an associative polymer, an organic microparticle, a siliceous material and optionally further comprising cellulose fiber is disclosed.
• the present invention provides for a synergistic combination comprising a water soluble copolymer prepared under certain conditions (Hereinafter referred to as "associative polymer”) and an organic microparticle. It has surprising been found that this synergistic combination results in retention and drainage performance superior to that of the individual components.
• the present invention also provides for a novel composition comprising an associative polymer and an organic microparticle.
• the present invention also provides for a novel composition comprising an associative polymer, an organic microparticle and a siliceous material.
• the present invention also provides for a novel composition comprising an associative polymer, an organic microparticle, and cellulose fiber.
• the present invention also provides for a novel composition
• a novel composition comprising an associative polymer, an organic microparticle, a siliceous material and cellulose fiber.
• the use of the associative polymer as a retention and drainage aid has an impact on the performance of other additives in the papermaking system. Improved retention and/or drainage can have both a direct and indirect impact.
• a direct impact refers to the retention and drainage aid acting to retain the additive.
• An indirect impact refers to the efficacy of the retention and drainage aid to retain filler and fines onto which the additive is attached by either physical or chemical means.
• filler refers to particulate materials, typically inorganic in nature, that are added to the cellulosic pulp slurry to provide certain attributes or be a lower cost substitute of a portion of the cellulose fiber.
• Their relatively small size, on the order of 0.2 to 10 microns, low aspect ratio and chemical nature results in their not being adsorbed onto the large fibers yet too small to be entrapped in the fiber network that is the paper sheet.
• fines refers to small cellulose fibers or fibrils, typically less than 0.2 mm in length and /or ability to pass through a 200 mesh screen.
• the amount of additive retained in the sheet increases. This can provide either an enhancement of the property, providing a sheet with increased performance attribute, or allows the papermaker to reduce the amount of additive added to the system, reducing the cost of the product. Moreover, the amount of these materials in the recirculating water, or Whitewater, used in the papermaking system is reduced. This reduced level of material, that under some conditions can be considered to be an undesirable contaminant, can provide a more efficient papermaking process or reduce the need for scavengers or other materials added to control the level of undesirable material.
• additive refers to materials added to the paper slurry to provide specific attributes to the paper and/or improve the efficiency of the papermaking process. These materials include, but are not limited to, sizing agents, wet strength resins, dry strength resins, starch and starch derivatives, dyes, contaminant control agents, antifoams, and biocides.
• the associative polymer useful in the present invention can be described as follows:
• a water-soluble copolymer composition comprising the formula:
• B is a nonionic polymer segment formed from the polymerization of one or more ethylenically unsaturated nonionic monomers
• F is an anionic, cationic or a combination of anionic and cationic polymer segment(s) formed from polymerization of one or more ethylenically unsaturated anionic and/or cationic monomers
• the molar % ratio of B:F is from 95:5 to 5:95
• the water-soluble copolymer is prepared via a water-in-oil emulsion polymerization technique that employs at least one emulsification surfactant consisting of at least one diblock or triblock polymeric surfactant wherein the ratio of the at least one diblock or triblock surfactant to monomer is at least about 3:100 and wherein;
• the water-in- oil emulsion polymerization technique comprises the steps of: (a) preparing an aqueous solution of monomers, (b) contacting the aqueous solution with a
• 0.0025 wt. % to 0.025 wt. % of the copolymer in 0.01 M NaCI is greater than 0.75 and the storage modulus (G') for a 1.5 wt. % actives copolymer solution at 4.6 Hz greater than 175 Pa.
• the associative polymer can be a cationic copolymer.
• the cationic copolymer is characterized in that its Huggins 1 constant (k 1 ) determined between 0.0025 wt. % to 0.025 wt. % of the copolymer in 0.01 M NaCI is greater than 0.5; and it has a storage modulus (G') for a 1.5 wt. % actives copolymer solution at 6.3 Hz greater than 50 Pa.
• the associative polymer can be an amphoteric copolymer.
• the amphoteric copolymer is characterized in that its Huggins' constant (k 1 ) determined between 0.0025 wt. % to 0.025 wt. % of the copolymer in 0.01 M NaCI is greater than 0.5; and the copolymer has a storage modulus (G') for a 1.5 wt. % actives copolymer solution at 6.3 Hz greater than 50 Pa.
• Inverse emulsion polymerization is a standard chemical process for preparing high molecular weight water-soluble polymers or copolymers.
• an inverse emulsion polymerization process is conducted by 1) preparing an aqueous solution of the monomers, 2) contacting the aqueous solution with a hydrocarbon liquid containing appropriate emulsification surfactant(s) or surfactant mixture to form an inverse monomer emulsion, 3) subjecting the monomer emulsion to free radical polymerization, and, optionally, 4) adding a breaker surfactant to enhance the inversion of the emulsion when added to water.
• Inverse emulsions polymers are typically water-soluble polymers based upon ionic or non-ionic monomers. Polymers containing two or more monomers, also referred to as copolymers, can be prepared by the same process. These co-monomers can be anionic, cationic, zwitterionic, nonionic, or a combination thereof.
• Typical nonionic monomers include, but are not limited to, acrylamide; methacrylamide; N-alkylacrylamides, such as N-methylacrylamide; N,N-dialkylacrylamides, such as N,N-dimethylacrylamide; methyl acrylate; methyl methacrylate; acrylonitrile; N-vinyl methylacetamide; N-vinyl formamide; N-vinyl methyl formamide; vinyl acetate; N-vinyl pyrrolidone; hydroxyalky(meth)acrylates such as hydroxyethyl(meth)acrylate or hydroxypropyl(meth)acrylate; mixtures of any of the foregoing and the like.
• Nonionic monomers of a more hydrophobic nature can also be used in the preparation of the associative polymer.
• the term 'more hydrophobic' is used here to indicate that these monomers have reduced solubility in aqueous solutions; this reduction can be to essentially zero, meaning that the monomer is not soluble in water. It is noted that the monomers of interest are also referred to as polymerizable surfactants or surfmers.
• These monomers include, but are not limited to, alkylacryamides; ethylenically unsaturated monomers that have pendant aromatic and alkyl groups, and ethers of the formula where R' is hydrogen or methyl; A is a polymer of one or more cyclic ethers such as ethyleneoxide, propylene oxide and/or butylene oxide; and R is a hydrophobic group; vinylalkoxylates; allyl alkoxylates; and allyl phenyl polyolether sulfates.
• Exemplary materials include, but are not limited to, methylmethacrylate, styrene, t-octyl acrylamide, and an allyl phenyl polyol ether sulfate marketed by Clariant as Emulsogen APG 2019.
• Exemplary anionic monomers include, but are not limited to, the free acids and salts of: acrylic acid; methacrylic acid; maleic acid; itaconic acid; acrylamidoglycolic acid; 2-acrylamido-2-methyl-1-propanesulfonic acid; 3- allyloxy-2-hydroxy-1-propanesulfonic acid; styrenesulfonic acid; vinylsulfonic acid; vinylphosphonic acid; 2-acrylamido-2-methylpropane phosphonic acid; mixtures of any of the foregoing and the like.
• Exemplary cationic monomers include, but are not limited to, cationic ethylenically unsaturated monomers such as the free base or salt of: diallyldialkylammonium halides, such as diallyldimethylammonium chloride; the (meth)acrylates of dialkylaminoalkyl compounds, such as dimethylaminoethyl (meth)acrylate, diethylaminoethyi (meth)acrylate, dimethyl aminopropyl (meth)acrylate, 2-hydroxydimethyl aminopropyl (meth)acrylate, aminoethyl (meth)acrylate, and the salts and quaternaries thereof; the N 1 N- dialkylaminoalkyl(meth)acrylamides, such as N,N-dimethylaminoethylacrylamide, and the salts and quaternaries thereof and mixture of the foregoing and the like.
• the co-monomers may be present in any ratio.
• the molar ratio of nonionic monomer to anionic monomer may fall within the range of 95:5 to 5:95, preferably the range is from about 75:25 to about 25:75 and even more preferably the range is from about 65:35 to about 35:65 and most preferably from about 60:40 to about 40:60.
• the molar percentages of B and F must add up to 100%. It is to be understood that more than one kind of nonionic monomer may be present in the Formula I. It is also to be understood that more than one kind of anionic monomer may be present in the Formula I.
• the associative polymer when it is an anionic copolymer, is defined by Formula I where B, the nonionic polymer segment, is the repeat unit formed after polymerization of acrylamide; and F, the anionic polymer segment, is the repeat unit formed after polymerization of a salt or free acid of acrylic acid and the molar percent ratio of B:F is from about 75:25 to about 25:75
• the physical characteristics of the associative polymer, when it is an anionic copolymer, are unique in that their Huggins' constant (k 1 ) as determined in 0.01 M NaCI is greater than 0.75 and the storage modulus (G') for a 1.5 wt. % actives polymer solution at 4.6 Hz is greater than 175 Pa, preferably greater than 190 and even more preferably greater than 205.
• the Huggins 1 constant is greater than 0.75, preferably greater than 0.9 and even more preferably greater than 1.0
• the molar ratio of nonionic monomer to cationic monomer may fall within the range of 99:1 to 50:50, or 95:5 to 50:50, or 95:5 to 75:25, or 90:10 to 60:45, preferably the range is from about 85:15 to about 60:40 and even more preferably the range is from about 80:20 to about 50:50.
• the molar percentages of B and F must add up to 100%. It is to be understood that more than one kind of nonionic monomer may be present in the Formula I. It is also to be understood that more than one kind of cationic monomer may be present in the Formula I.
• the minimum amount of each of the anionic, cationic and non-ionic monomer is 1% of the total amount of monomer used to form the copolymer.
• the maximum amount of the non-ionic, anionic or cationic is 98% of the total amount of monomer used to form the copolymer.
• the minimum amount of any of anionic, cationic and non-ionic monomer is 5%, more preferably the minimum amount of any of anionic, cationic and non-ionic monomer is 7% and even more preferably the minimum amount of any of anionic, cationic and non-ionic monomer is 10% of the total amount of monomer used to form the copolymer.
• the molar percentages of anionic, cationic and non-ionic monomer must add up to 100%. It is to be understood that more than one kind of nonionic monomer may be present in the Formula I, more than one kind of cationic monomer may be present in the Formula I, and that more than one kind of anionic monomer may be present in the Formula I.
• the physical characteristics of the associative polymer when it is a cationic or amphoteric copolymer, are unique in that their Huggins 1 constant (k 1 ) as determined in 0.01 M NaCI is greater than 0.5 and the storage modulus (G') for a 1.5 wt. % actives polymer solution at 6.3 Hz is greater than 50 Pa, preferably greater than 10 and even more preferably greater than 25, or greater than 50, or greater than 100, or greater than 175, or greater than 200.
• the Huggins 1 constant is greater than 0.5, preferably greater than 0.6, or greater than 0.75, or greater than 0.9 or greater than 1.0.
• the emulsification surfactant or surfactant mixture used in an inverse emulsion polymerization system have an important effect on both the manufacturing process and the resultant product.
• Surfactants used in emulsion polymerization systems are known to those skilled in the art. These surfactants typically have a range of HLB (Hydrophilic Lipophilic Balance) values that is dependent on the overall composition.
• HLB Hydrophilic Lipophilic Balance
• One or more emulsification surfactants can be used.
• the emulsification surfactant(s) of the polymerization products that are used to produce the associative polymer include at least one diblock or triblock polymeric surfactant. It is known that these surfactants are highly effective emulsion stabilizers.
• the choice and amount of the emulsification surfactant(s) are selected in order to yield an inverse monomer emulsion for polymerization.
• one or more surfactants are selected in order to obtain a specific HLB value.
• Diblock and triblock polymeric emulsification surfactants are used to provide unique materials.
• diblock and triblock polymeric emulsification surfactants are used in the necessary quantity, unique polymers exhibiting unique characteristic result, as described in WO 03/050152 A1 and US 2004/0143039 A1 , the entire contents of each is herein incorporated by reference.
• Exemplary diblock and triblock polymeric surfactants include, but are not limited to, diblock and triblock copolymers based on polyester derivatives of fatty acids and poly[ethyleneoxide] (e.g., Hypermer® B246SF, Uniqema, New Castle, DE), diblock and triblock copolymers based on polyisobutylene succinic anhydride and polyjethyleneoxide], reaction products of ethylene oxide and propylene oxide with ethylenediamine, mixtures of any of the foregoing and the like.
• the diblock and triblock copolymers are based on polyester derivatives of fatty acids and poly[ethyleneoxide].
• the triblock contains two hydrophobic regions and one hydrophilic region, i.e., hydrophobe-hydrophile-hydrophobe.
• the amount (based on weight percent) of diblock or triblock surfactant is dependent on the amount of monomer used to form the associative polymer.
• the ratio of diblock or triblock surfactant to monomer is at least about 3 to 100.
• the amount of diblock or triblock surfactant to monomer can be greater than 3 to 100 and preferably is at least about 4 to 100 and more preferably 5 to 100 and even more preferably about 6 to 100.
• the diblock or triblock surfactant is the primary surfactant of the emulsification system.
• a secondary emulsification surfactant can be added to ease handling and processing, to improve emulsion stability, and/or to alter the emulsion viscosity.
• secondary emulsification surfactants include, but are not limited to, sorbitan fatty acid esters, such as sorbitan monooleate (e.g., Atlas G-946, Uniqema, New Castle, DE), ethoxylated sorbitan fatty acid esters, polyethoxylated sorbitan fatty acid esters, the ethylene oxide and/or propylene oxide adducts of alkylphenols, the ethylene oxide and/or propylene oxide adducts of long chain alcohols or fatty acids, mixed ethylene oxide/propylene oxide block copolymers, alkanolamides, sulfosuccinates and mixtures thereof and the like.
• sorbitan fatty acid esters such as sorbitan monooleate (e.g., Atlas G-946
• Polymerization of the inverse emulsion may be carried out in any manner known to those skilled in the art. Examples can be found in many references, including, for example, Allcock and Lampe, Contemporary Polymer Chemistry, (Englewood Cliffs, New Jersey, PRENTICE-HALL, 1981), chapters 3- 5.
• a representative inverse emulsion polymerization is prepared as follows. To a suitable reaction flask equipped with an overhead mechanical stirrer, thermometer, nitrogen sparge tube, and condenser is charged an oil phase of paraffin oil (135.Og, Exxsol® D80 oil, Exxon - Houston, TX) and surfactants (4.5g Atlas® G-946 and 9.Og Hypermer® B246SF). The temperature of the oil phase is then adjusted to 37°C.
• paraffin oil (135.Og, Exxsol® D80 oil, Exxon - Houston, TX
• surfactants 4.5g Atlas® G-946 and 9.Og Hypermer® B246SF
• An aqueous phase is prepared separately which comprised 53-wt. % acrylamide solution in water (126.5g), acrylic acid (68.7g), deionized water (70.Og), and Versenex® 80 (Dow Chemical) chelant solution (0.7g).
• the aqueous phase is then adjusted to pH 5.4 with the addition of ammonium hydroxide solution in water (33.1g, 29.4 wt. % as NH 3 ).
• the temperature of the aqueous phase after neutralization is 39°C.
• the aqueous phase is then charged to the oil phase while simultaneously mixing with a homogenizer to obtain a stable water-in-oil emulsion.
• This emulsion is then mixed with a 4-blade glass stirrer while being sparged with nitrogen for 60 minutes. During the nitrogen sparge the temperature of the emulsion is adjusted to 50+1 0 C. Afterwards, the sparge is discontinued and a nitrogen blanket implemented.
• the polymerization is initiated by feeding a 3-wt. % solution of 2,2'- azobisisobutyronitrile (AIBN) in toluene (0.213g). This corresponds to an initial AIBN charge, as AIBN, of 250 ppm on a total monomer basis.
• AIBN 2,2'- azobisisobutyronitrile
• the batch temperature was allowed to exotherm to 62°C ( ⁇ 50 minutes), after which the batch was maintained at 62+1 0 C. After the feed the batch was held at 62+1 0 C for 1 hour.
• 3-wt. % AIBN solution in toluene (0.085g) is then charged in under one minute. This corresponds to a second AIBN charge of 100 ppm on a total monomer basis.
• the associative polymer emulsion is typically inverted at the application site resulting in an aqueous solution of 0.1 to 1% active copolymer. This dilute solution of the associative polymer is then added to the paper process to affect retention and drainage.
• the associative polymer may be added to the thick stock or thin stock, preferably the thin stock.
• the associative polymer may be added at one feed point, or may be split fed such that the associative polymer is fed simultaneously to two or more separate feed points. Typical stock addition points include feed point(s) before the fan pump, after the fan pump and before the pressure screen, or after the pressure screen.
• the associative polymer may be added in any effective amount to achieve flocculation.
• the amount of copolymer could be more than 0.5 Kg per metric ton of cellulosic pulp (dry basis).
• the associative polymer is employed in an amount of at least about 0.03 Ib. to about 0.5 Kg. of active copolymer per metric ton of cellulosic pulp, based on the dry weight of the pulp.
• the concentration of copolymer is preferably from about 0.05 to about 0.5 Kg of active copolymer per metric ton of dried cellulosic pulp.
• the copolymer is added in an amount of from about 0.05 to 0.4 Kg per metric ton cellulose pulp and, most preferably, about 0.1 to about 0.3 Kg per metric ton based on dry weight of the cellulosic pulp.
• the second component of the retention and drainage system can be an organic microparticle (also know as a micropolymer or a microbead)
• organic microparticles are crosslinked, ionic, organic polymeric materials. They are copolymers of a nonionic monomer, an ionic monomer and a crosslinking agent. Further, the ionic monomer may be anionic or cationic. Use of both anionic and cationic monomers in the same polymer results in an amphoteric material.
• microparticles are typically formed by the polymerization of ethylenically unsaturated monomers that can be anionic, cationic or non-ionic. Inverse emulsion polymerization is typically used to prepare these materials although other polymerization methods known to those skilled in the art can be used.
• the preferred ethylenically unsaturated non-ionic monomers in preparing the organic microparticle are selected from acrylamide; methacrylamide; N,N-dialkylacrylamides; N-alkylacrylamides; N-vinyl methacetamide; N-vinyl formamide, N-vinyl methylformamide; N-vinyl pyrrolidone; and mixtures thereof.
• Exemplary anionic monomers used in preparing the organic microparticle include, but are not limited to, the salts and free acid of: acrylic acid, methacrylic acid, ethylacrylic acid, 2-acrylamido-2-alkylsulfonic acids where the alkyl group contains 1 to 6 carbon atoms, such as 2-acrylamido-2-propane- sulfonic acid or mixtures of any of the foregoing and the like; and their alkaline salts.
• the salts or acids of acrylic acid, methacrylic acid, and 2-acrylamido-2-methylpropane sulfonic acid have sodium as the cation
• Exemplary cationic monomers used in preparing the organic microparticle include, but are not limited to , ethylenically unsaturated monomers selected from the free base or salts of: acryloxyethyltrimethylammonium chloride; diallydimethylammonium chloride; 3-(meth)acrylamido-propyltrimethylammonium chloride; S-acrylamido-propyltrimethylammonium ⁇ -hydroxypropylacrylate methosulfate; trimethylammoniumethyl methacrylate methosuifate; 1- trimethylammonium-2-hydroxypropyl-nnethacrylate methosulfate; methacryloxyethyltri-methylammonium chloride; and mixtures of any of the foregoing and the like.
• These ethylenically unsaturated anionic, cationic and nonionic monomers that make up the organic microparticle may be polymerized to form anionic, cationic or amphoteric copolymers, with the three types of monomer present in any ratio.
• Acrylamide is the preferred nonionic monomer.
• polyfunctional crosslinking agent comprises molecules that have at least two double bonds, or a double bond and reactive group, or two reactive groups.
• Examples of the polyfunctional cross-linking agent containing at least two double bonds include, but are not limited to N,N-methylenebisacrylamide, N, N- methylenebismethacrylamide, polyethyleneglycol diacrylate, polyethyleneglycol dimethacrylate, N-vinyl acrylamide, divinylbenzene, triallylammonium salts, N- methyallylacrylamide and the like.
• polyfunctional cross-linking or branching agent containing at least one double bond and at least one reactive group examples include, but are not limited to, glycidyl acrylate, acrolein, methylolacrylamide and the like.
• polyfunctional branching agents containing at least two reactive groups include, but are not limited to, aldehydes such as glyoxal, diepoxy compounds, epichlorohydrin and the like.
• Crosslinking agents are to be used in sufficient quantities to assure a crosslinked composition.
• An example of an organic microparticle is disclosed in US 5,171 ,808. Microparticles are commercially available under the trade name Polyflex® CP.3 (Ciba, Tarrytown, NY).
• the second component of the retention and drainage system can be added at amounts up to 0.5 Kg of active material per metric ton of cellulose pulp based on dry weight of the pulp, with the ratio of the associative polymer to second component being 1 :100 to 100:1. It is contemplated that more than one second component can be used in the papermaking system.
• siliceous materials can be used as an additional component of a retention and drainage aid used in making paper and paperboard.
• the siliceous material may be any of the materials selected from the group consisting of silica based particles, silica microgels, amorphous silica, colloidal silica, anionic colloidal silica, silica sols, silica gels, polysilicates, polysilicic acid, and the like. These materials are characterized by the high surface area, high charge density and submicron particle size.
• This group includes stable colloidal dispersion of spherical amorphous silica particles, referred to in the art as silica sols.
• the term sol refers to a stable colloidal dispersion of spherical amorphous particles.
• Silica gels are three dimensional silica aggregate chains, each comprising several amorphous silica sol particles, that can also be used in retention and drainage aid systems; the chains may be linear or branched.
• Silica sols and gels are prepared by polymerizing monomeric silicic acid into a cyclic structure that result in discrete amorphous silica sols of polysilicic acid. These silica sols can be reacted further to produce a three dimensional gell network.
• the various silica particles (sols, gels, etc.) can have an overall size of 5-50 nm.
• Anionic colloidal silica can also be used.
• the siliceous material can be added to the cellulosic suspension in an amount of at least 0.005 Kg per metric ton based on dry weight of the cellulosic suspension.
• the amount of siliceous material may be as high at 50 Kg per metric ton.
• the amount of siliceous material is from about 0.05 to about 25 Kg per metric ton. Even more preferably, the amount of siliceous material is from about 0.25 to about 5 Kg per metric ton based on the dry weight of the cellullosic suspension.
• an additional component of the retention and drainage aid system can be a conventional flocculant.
• a conventional flocculant is generally a linear cationic or anionic copolymer of acrylamide.
• the additional component of the retention and drainage system is added in conjunction with the aluminum compound and the associative polymer to provide a multi-component system which improves retention and drainage.
• the conventional flocculant can be an anionic, cationic or non-ionic polymer.
• the ionic monomers are most often used to make copolymers with a non-ionic monomer such as acrylamide.
• These polymers can be provided by a variety of synthetic processes including, but not limited to, suspension, dispersion and inverse emulsion polymerization. For the last process, a microemulsion may also be used.
• the co-monomers of the conventional flocculant may be present in any ratio.
• the resultant copolymer can be non-ionic, cationic, anionic, or amphoteric (contains both cationic and anionic charge).
• Yet other additional components that can be part of the inventive system are aluminum sources, such as alum (aluminum sulfate), polyaluminum sulfate, polyaluminum chloride and aluminum chlorohydrate.
• the components of a retention and drainage system may be added substantially simultaneously to the cellulosic suspension.
• retention and drainage system is used here to encompass two or more distinct materials added to the papermaking slurry to provide improved retention and drainage.
• the components may be added to the cellulosic suspension separately either at the same stage or dosing point or at different stages or dosing points.
• any two of more of the materials may be added as a blend.
• the mixture may be formed in-situ by combining the materials at the dosing point or in the feed line to the dosing point.
• the inventive system comprises a preformed blend of the materials.
• the components of the inventive system are added sequentially. A shear point may or may not be present between the addition points of the components.
• the components can be added in any order.
• the inventive system is typically added to the paper process to affect retention and drainage.
• the inventive system may be added to the thick stock or thin stock, preferably the thin stock.
• the system may be added at one feed point, or may be split fed such that the inventive system is fed simultaneously to two or more separate feed points.
• Typical stock addition points include feed points(s) before the fan pump, after the fan pump and before the pressure screen, or after the pressure screen.
• a series of drainage tests were conducted utilizing a synthetic alkaline furnish.
• This furnish is prepared from hardwood and softwood dried market lap pulps, and from water and further materials.
• the hardwood and softwood dried market lap pulp are refined separately. These pulps are then combined at a ratio of about 70 percent by weight of hardwood to about 30 percent by weight of soft wood, in an aqueous medium.
• the aqueous medium utilized in preparing the furnish comprises a mixture of local hard water and deionized water to a representative hardness.
• Inorganic salts are added in amounts so as to provide this medium with a total alkalinity of 75 ppm as CaCO 3 and hardness of 100 ppm as CaCO 3 ..
• Precipitated calcium carbonate is introduced into the pulp furnish at a representative weight percent to provide a final furnish containing 80% fiber and 20% PCC filler.
• the drainage tests were conducted by mixing the furnish with a mechanical mixer at a specified mixer speed, and introducing the various chemical components into the furnish and allowing the individual components to mix for a specified time prior to the addition of the next component.
• the specific chemical components and dosage levels are described in the data tables.
• the drainage activity of the invention was determined utilizing the Canadian Standard Freeness (CSF) .
• CSF test a commercially available device (Lorentzen & Wettre, Sweden), can be utilized to determine relative drainage rate or dewatering rate is also known in the art; standard test method (TAPPI Test Procedure T-227) is typical.
• the CSF device consists of a drainage chamber and a rate measuring funnel, both mounted on a suitable support.
• the CSF drainage tests are conducted with 1 liter of the furnish.
• the furnish is prepared for the described treatment externally from the CSF device in a square beaker to provide turbulent mixing.
• the treated furnish is poured into the drainage chamber, closing the top lid, and them immediately opening the bottom plate.
• the water is allowed to drain freely into the rate-measuring funnel; water flow that exceeds that determined by the bottom orifice will overflow through the side orifice and is collected in a graduated cylinder.
• the values generated are described in milliliters (ml) of filtrate; higher quantitative values represent higher levels of drainage or dewatering.
• Table 1 illustrates the utility of the invention.
• the test samples were prepared as follows: the furnish prepared as described above, is added, first, 5 Kg of cationic starch (Stalok® 400, AE., Staley, Decatur, IL) per metric ton of furnish (dry basis). Next, 2.5 Kg of alum (aluminum sulfate octadecahydrate obtained from Delta Chemical Corporation, Baltimore, MD as a 50% solution) per metric ton of furnish (dry basis) is added, followed by 0.25 Kg of PerForm® PC8138 cationic polymer (Hercules Incorporated, Wilmington, DE) per metric ton of furnish (dry basis).
• alum aluminum sulfate octadecahydrate obtained from Delta Chemical Corporation, Baltimore, MD as a 50% solution
• PerForm® PC8138 cationic polymer Hercules Incorporated, Wilmington, DE
• SP9232 is PerForm® SP9232, a retention and drainage aid associative polymer (see PCT WO 03/050152 A), is a product of Hercules Incorporated, Wilmington, DE; Polyflex is Polyflex CP.3, an organic microparticle marketed by Ciba Specialty Chemicals, Tarrytown, NY; and silica is NP780, a colloidal silica product of Eka Chemicals, Marietta, GA.

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• 2005
  • 2005-12-22 AU AU2005322256A patent/AU2005322256A1/en not_active Abandoned
  • 2005-12-22 EP EP05854764A patent/EP1844193A1/en not_active Withdrawn
  • 2005-12-22 WO PCT/US2005/046104 patent/WO2006071633A1/en active Application Filing
  • 2005-12-22 KR KR1020077017372A patent/KR20070103398A/ko not_active Application Discontinuation
  • 2005-12-22 CA CA002592230A patent/CA2592230A1/en not_active Abandoned

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