US20120285644A1 - Functionalization of paper components - Google Patents

Functionalization of paper components Download PDF

Info

Publication number
US20120285644A1
US20120285644A1 US13/369,392 US201213369392A US2012285644A1 US 20120285644 A1 US20120285644 A1 US 20120285644A1 US 201213369392 A US201213369392 A US 201213369392A US 2012285644 A1 US2012285644 A1 US 2012285644A1
Authority
US
United States
Prior art keywords
polymer
paper
amine
pulp
complementary
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US13/369,392
Inventor
David S. Soane
Michael C. Berg
William A. Mowers
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NanoPaper LLC
Original Assignee
NanoPaper LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by NanoPaper LLC filed Critical NanoPaper LLC
Priority to US13/369,392 priority Critical patent/US20120285644A1/en
Publication of US20120285644A1 publication Critical patent/US20120285644A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/34Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/41Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
    • D21H17/44Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups cationic
    • D21H17/45Nitrogen-containing groups
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/21Macromolecular organic compounds of natural origin; Derivatives thereof
    • D21H17/24Polysaccharides
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H21/00Non-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
    • D21H21/14Non-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
    • D21H21/18Reinforcing agents

Definitions

  • the technical field of the invention relates to compositions and methods for enhancing the properties of materials such as paper-related products.
  • Paper manufacturing is an important industrial process, resulting in the production of a vast variety of products. Paper products often times include the use of filler materials, which allow products to be produced more cheaply. The use of fillers, however, can decrease the quality of the product in terms of strength, appearance, and other features. Though additives have been derived for further improving the quality of manufactured paper, a need persists for processes and compositions that further improve the quality of paper. Indeed, the development of additives which result in improved efficiency and lower cost production is desirable.
  • compositions and methods disclosed herein relate to methods for enhancing the mechanical properties of paper.
  • these compositions and methods can relate to improving the economics of papermaking, or can enable paper fibers to be used in other applications where presently their use has been limited by their mechanical properties.
  • the techniques disclosed herein can enhance other advantageous properties of paper, such as the hydrophobicity of paper.
  • the pulp and/or filler to be used in making a paper sheet can be functionalized with an amine-containing polymer.
  • a complimentary polymer can be added either sequentially or in an emulsion form. When performed sequentially, the complimentary polymer can be added either before or after the formation of a paper sheet.
  • a mixture which can be used for producing a paper-based material.
  • the mixture can include an aqueous medium, a pulp comprising fibers, filler particles, and an amine-containing polymer.
  • the amine-containing polymer can enhance properties of either the mixture or a paper-based material to be produced from the mixture.
  • the fibers of the pulp can be substantially free of synthetic polymer-based fibers, and/or can have a net negative charge.
  • the filler particles can have an inorganic surface, and can include one or more of calcium carbonate, kaolin, and titanium dioxide.
  • the amine-containing polymer can be adapted to functionalize a surface of the filler particles.
  • the fibers of the pulp are not substantially functionalized by the amine-containing polymer.
  • the amine-containing polymer can be substantially coupled to, or functionalize, only one of the pulp and the filler particles.
  • Amine-containing polymers used in some embodiments can include at least one of a homopolymer and a copolymer.
  • the amine-containing polymer can also include at least a polycationic segment such as at least one segment of chitosan, polyalkyleneimine, polyvinyl amine, and polyallyl amine.
  • the amine-containing polymer includes one or more segments of any one of chitosan and branched polyethyleneimine.
  • One or more crosslinking agents e.g., a silane coupling agent
  • a crosslinking agent can include two or more functionalities for reacting with the amine-containing polymer and/or a paper making component (e.g., filler particles, pulp fibers, or both).
  • a complementary polymer can be included for enhancing the properties of a mixture or a paper-based material.
  • Such embodiments can be utilized when both a pulp and filler particles are functionalized by an amine-containing polymer, though only one of the pulp and fillers can be functionalized as well.
  • one exemplary embodiment can be drawn to a mixture including an aqueous medium; a pulp with fibers; an amine-containing polymer for functionalizing a surface of the fibers; and a complementary polymer capable of coupling with the amine-containing polymer.
  • the complementary polymer can be capable of coupling with the amine-containing polymer, either through reaction or some nonreactive interaction (e.g., electrostatic attraction). This can couple a portion of the pulp with a portion of the filler when the amine-containing polymer functionalizes both components.
  • Complementary polymers can be polyanionic, and can be a homopolymer, copolymer, or any combination thereof.
  • the complementary polymer can also include one or more epoxide, anhydride (e.g., maleic anhydride), carboxylic acid, and isocynate groups.
  • Non-limiting examples of complementary polymers include polymers that have at least one polymer segment of pectin, xanthan gum, carboxymethyl cellulose, polyacrylic acid, and polymethacrylic acid.
  • Other types of complementary polymers can have an elastomeric component or a component that increases water resistance of a paper-based material.
  • the amine-containing polymer can emulsify the complementary polymer (e.g., a polymer that is substantially insoluble in water).
  • fibers of a pulp are functionalized using an amine-containing polymer.
  • Filler particles can be combined with the functionalized fibers of the pulp to produce at least a portion of a paper-forming mixture.
  • the mixture can be used to produce a paper-based material.
  • the amine-containing polymer optionally does not functionalize the filler particles.
  • the filler particles are functionalized with the amine-containing polymer.
  • the pulp can be combined with the functionalized filler particles to form the portion of the paper-forming mixture.
  • the amine-containing polymer optionally does not functionalize the pulp (e.g., the fibers of the pulp). It is also understood that in some of these embodiments, both the filler and the pulp can be functionalized by the amine-containing polymer.
  • the methods can include any of the mixtures described herein as well.
  • the functionalization of fibers of pulp, or filler particles can be achieved by combining the component with an amine-containing polymer that can include chitosan segments and/or branched polyethyleneimine segments.
  • the pulp or filler particles can be combined with chitosan to form a functionalizing mixture.
  • the pH of the functionalizing mixture can be raised to at least about 6 to cause the chitosan to associate with the pulp and/or filler particles.
  • Embodiments drawn to methods of producing paper-based materials can also utilize a complementary polymer, the use of which can be consistent with other embodiments disclosed herein.
  • the complementary polymer can be capable of coupling with the amine-containing polymer, through any combination of chemical reaction and nonreactive interaction mechanisms (e.g., electrostatic interactions).
  • the complementary polymer can provide one or more enhanced properties to the produced paper material relative to materials that do not utilize a complementary polymer.
  • Non-limiting examples of enhanced properties include mechanical properties such as strength, stiffness, wear resistance, water resistance (e.g., though increased water contact angle), and elasticity.
  • a sheet can be formed using the paper-forming mixture, where the complementary polymer can be added either before or after the sheet is formed.
  • the addition can occur either before or after the sheet is dried.
  • functionalizing either the fibers of a pulp or the filler particles can include emulsifying the complementary polymer with the amine-containing polymer (e.g., a hydrophobic polymer), and adding the emulsion to the component being functionalized.
  • the term “functionalization” and “functionalize” refer to a change in one or more aspects of the physicochemical nature of an entity.
  • functionalization of a particle surface refers to a change in one or more aspects of the particle surface, which result in some physicochemical change in how the particle surface interacts with other entities.
  • functionalization of an entity can result in a change in some macroscopic property (e.g., tensile strength) when the functionalized entity is used to produce a product due to the associations of the functionalized entity with other components, or even with other functionalized entities.
  • Functionalization can also alter the types of chemical reactions that an entity can be subjected to relative to when the entity is not functionalized.
  • polymer refers to a molecule comprising a plurality of repeat units or monomers.
  • a polymer can comprise one or more distinct repeat units.
  • a “copolymer” refers to a polymer having two or more distinct repeat units. Repeat units can be arranged in a variety of manners. For example, a homopolymer refers to a polymer with one type of repeat unit where the repeat units are adjacently connected. In another example, a plurality of different repeat units can be assembled as a copolymer. If A represents one repeat unit and B represents another repeat unit, copolymers can be represented as blocks of joined units (e.g., A-A-A-A-A-A . . .
  • B-B-B-B-B-B-B-B . . . or interstitially spaced units (e.g., A-B-A-B-A-B . . . or A-A-B-A-A-B-A-A-B . . . ), or randomly arranged units.
  • these representations can be made with 3 or more types of repeat units as well.
  • polymers e.g., homopolymers or copolymers
  • macromolecules in a broad range of configurations e.g., cross-linked, linear, and/or branched).
  • segment refers to a portion of a polymer that includes one or more units.
  • a segment can include one or more types of units (e.g., A-A-A-A or A-B-C-A-C).
  • Some embodiments are directed to compositions and methods for producing materials such as paper-based materials.
  • Such embodiments can utilize an amine-containing polymer, which can be a polycation.
  • the amine-containing polymer can associate with one or more components of a mixture (e.g., a paper-making mixture).
  • Components can include pulp fibers, the surfaces of a particle filler, and other elements or portions of the elements.
  • the association of the amine-containing polymer with any particular component can functionalize that component, potentially increasing the strength, or improving one or more other qualities, of a paper product produced with compositions consistent with such embodiments.
  • some exemplary embodiments are directed to mixtures that can be used to produce various materials, such as paper-based materials.
  • mixtures can include any number of typical components utilized in commercial paper making
  • some embodiments include a solution medium (e.g., an aqueous solution), a pulp material, and filler particles.
  • the mixtures can include an amine-containing polymer, which can associate and/or interact with one or more components of the mixture.
  • the amine-containing polymer can functionalize the component of the mixture with which the polymer interacts.
  • the amine-containing polymer can functionalize the particle filler component (e.g., the surface of the filler particles), but does not substantially functionalize the pulp.
  • the amine-containing polymer can functionalize the pulp (e.g., the fibers of the pulp), but does not substantially functionalize the filler component.
  • the amine-containing polymer functionalizes both the filler component and the pulp. Functionalization can and cannot also optionally occur with other components in a selective manner.
  • Functionalization of one or more components of a paper-making mixture with an amine-containing polymer can result in the enhancement of one or more properties of the mixture or a paper product formed from the mixture, relative to the properties when functionalization of the component is absent.
  • functionalization of one or more components can lead to an enhancement of mechanical properties of a paper product, e.g., tensile strength.
  • some embodiments can utilize functionalization of both components, some particular embodiments only functionalize one of the two components, while leaving the other component substantially unfunctionalized, i.e., either the pulp or the filler particles are functionalized, not both. It has surprisingly been found that in some instances, only functionalizing the pulp or the filler particles, but not both components, can lead to paper products that are stronger, or about as strong, relative to both components being functionalized.
  • average molecular weight of an amine-containing polymer it is understood that such average molecular weights can be applied to any described polymer (e.g., homopolymers or copolymers of any particular type of polymer such as branched polyethyleneimine or polyvinylamine). It is further understood that those skilled in the art will appreciate variations and combinations of the described features that are also within the scope of the present disclosure.
  • an amine-containing polymer can be any homopolymer or copolymer that has at least a portion of its repeat units containing an amine (e.g., quaternary, ternary, secondary or primary).
  • the amine-containing polymer can contain repeat units with primary amines due to the reactivity of the primary amine.
  • the amine-containing polymer is a polycation. Polycations can be advantageously utilized, for example, when the components sought to be functionalized have a net negative charge. In such instances, the use of electrostatic interactions with pulp fibers and/or filler can be effective in certain embodiments when the pulp fibers and/or filler have an inherent negative charge that can interact with the polycation.
  • amine-containing polymers can be utilized with various embodiments that include one or more different types of amine-containing polymers.
  • Amine-containing polymers can be naturally-occurring macromolecules with amine groups such as chitosan.
  • various types of synthetic polymers bearing amine groups such as polyalkyleneimines, polyvinylamine, polyallylamine, and polydiallylamine can be utilized.
  • copolymers comprising any combination of amine-containing homopolymer units can also be used.
  • Chitosan is an aminopolysaccharide typically prepared by deacetylation of chitin (poly-beta(1,4)-N-acetyl-D-glucosamine) obtained from marine organisms such as shrimp, crabs, lobsters, squid, and the like. Accordingly, it can be prepared with relative ease.
  • Branched polyethyleneimine herein “BPEI”) is an easily manufactured synthetic polymer that is also readily available at moderate cost.
  • some embodiments utilize chitosan, polyethyleneimine (such as BPEI), or a combination of the two polymers as separate homopolymers or as one or more copolymers.
  • BPEI polyethyleneimine
  • a combination of the two polymers as separate homopolymers or as one or more copolymers.
  • the average molecular weight of an amine-containing polymer is not necessarily limited, in some embodiments the average molecular weight of the amine-containing polymer can range from about 1,000 daltons to about 10,000,000 daltons; or from about 10,000 daltons to about 500,000 daltons. Such ranges can advantageously utilize amine-containing polymers which can be large enough to functionalize one or more components effectively, while not being so large as to effect the paper-making process.
  • Measurement of the average molecular weights for any polymer discussed herein can be with respect to a number of bases. For example, can be number averaged, weight averaged, or averaged based on some other weighting factors. As well, the techniques utilized to determine molecular weight can include the range of those known to those skilled in the art. Examples include gel permeation chromatography and light-scattering.
  • the average molecular weight can be difficult to ascertain.
  • Chitosan is an example of such an amine-containing polymer.
  • the average molecular weight of the polymer can be defined by some alternative parameter such as viscosity.
  • the chitosan has an average molecular weight defined by a viscosity range between about 10 centipoise and about 800 centipoise.
  • the viscosity can optionally be further defined by a set of conditions, such as being measured for a 1% solution of chitosan in pH 4 (or 0.1M) aqueous acetic acid at 25° C.
  • the pulp utilized in some embodiments disclosed herein can comprise fibers such as cellulose-based fibers, and can also include components typically found in pulps used to make paper products. Accordingly, the fibers of the pulp can have a net negative charge. Such charge can be utilized advantageously in some embodiments to cause electrostatic attraction of an amine-containing polymer that is, or is partially, a polycation.
  • the fibers of a pulp exclude the presence of synthetic fibers such as polymer-based fibers (e.g., aromatic amide fibers). Thus, some embodiments utilize pulps that include substantially naturally-occurring fibers.
  • Fillers utilized in some embodiments disclosed here can include particulates that are typically utilized as fillers in paper manufacturing applications.
  • the fillers can have a surface that is, at least partially, substantially inorganic in nature.
  • non-limiting examples of filler particles can include particles constructed from calcium, carbonate, kaolin, titanium dioxide, and other inorganic materials. Fillers can also be a composite of inorganics.
  • the surface of the fillers can have a net negative charge, which can tend to attract amine-containing polymers that are polycationic in nature.
  • functionalization of one or more components can be achieved by some type of coupling interaction between an amine-containing polymer and the component.
  • Such coupling can be achieved using either through a coupling agent or through electrostatic interactions that permit the polyamine to self-assemble onto the surface of the component.
  • electrostatic interactions with pulp fibers and filler can be effective in certain embodiments because both pulp fibers and filler have an inherent negative charge that can interact with the polyamine.
  • Coupling agents such as multifunctional crosslinking agents described herein, can be used to increase the amount of amine-containing polymer that can adhere to a surface, such as a surface of the filler particles.
  • multifunctional crosslinking agents can be used as a coupling agent. Such agents can react with at least one of the amine-containing polymer and the component to be coupled.
  • the multifunctional coupling agent can include a silicon containing coupling agent and at least one of the following functional groups: an epoxy group, a hydroxyl group, a carboxyl group, and/or an isocyano group.
  • the multifunctional coupling agent is a silane coupling agent.
  • the coupling agent does not include silicon (e.g., in embodiments in which silicon is not used).
  • the multifunctional coupling agent includes an isocyanosilane, for example, a trialkoxy isocyanosilane such as trimethoxy isocyanosilane, triethoxy isocyanosilane, and/or triisopropoxy isocyanosilane.
  • the multifunctional coupling agent includes an epoxy siloxane.
  • the multifunctional coupling agent can include triethoxy methacryloxypropyl silane. Other agents can also be employed as would be understood by those of skilled in the art.
  • functionalization of a paper making component can be achieved without the use of a coupling agent.
  • the amine-containing polymer can be added directly to a pulp stream, a filler stream, or to both, resulting in the association of the amine-containing polymer and the pulp, filler, or both.
  • the component can be functionalized by precipitating chitosan onto the surface of the component using, for example, a shift in pH. Since chitosan is only soluble in acidic conditions, the polymer can be made to precipitate when the pH is raised by adding a base to the solution after adding chitosan (e.g., to a pH of at least about 6).
  • the pH of the mixture can be in the range from about 4 to about 8; or from about 5 to about 8; or from about 6 to about 8.
  • some embodiments can utilize a mixture with one or more multivalent acids; non-limiting examples include citric, tartaric, aldaric (any in the family), oxalic, malonic, malic, succinic, glutaric, and adipic acid.
  • precipitation can occur spontaneously when a chitosan solution is added to a basic environment like a calcium carbonate solution.
  • the amount of chitosan to be added can be from about 0.01% to about 5.0% (based on weight of the component), or from about 0.1% to about 2%.
  • a complementary polymer can be added to a paper-making mixture.
  • the complementary polymer can be capable of coupling with an amine-containing polymer (e.g., the complementary polymer can react or nonreactively interact with the amine-containing polymer).
  • Such a complementary polymer can be used to enhance the properties of the mixture, or a resulting paper product produced from the mixture, relative to not using the complementary polymer.
  • the complementary polymer can be utilized when an amine-containing polymer is intended to functionalize pulp (e.g., fibers), filler particles, or both pulp and filler particles, among other paper-making mixture components.
  • the complementary polymer can be coupled with the amine-containing polymer, or can be free but will eventually couple with the amine-containing polymer.
  • the complementary polymer can be added to a process after an amine-containing polymer has functionalized one or more mixture components, or before functionalization has occurred such as in an emulsion technique described herein.
  • Some embodiments can utilize any complementary polymer (e.g., homopolymers, copolymers, and combinations of different polymers) which can interact nonreactively with an amine-containing polymer or which can react with the amine-containing polymer (e.g., reacting with an amine group).
  • the complementary polymer nonreactively interacts rather than reacts with the amine-containing polymer, the interaction may involve electrostatic forces, hydrogen bonds, or any other secondary interaction forces or association mechanisms.
  • the nonreactive interaction can be an electrostatic interaction when a polyanion is used as a portion or the entirety of the complementary polymer.
  • an appropriate polymer can also be used that includes repeat units with anionic charge.
  • the polyanion can include one or more carboxylic acid groups.
  • Non-limiting examples of suitable polyanions, or polyanion segments include biopolymers such as pectin, xanthum gum, and carboxymethyl cellulose, and synthetic polymers such as polyacrylic acid or polymethacrylic acid.
  • biopolymers such as pectin, xanthum gum, and carboxymethyl cellulose
  • synthetic polymers such as polyacrylic acid or polymethacrylic acid.
  • complementary polymers such as polyanions or polymers with polyanionic segments, can also be used consistent with the embodiments disclosed herein.
  • the complementary polymer when the complementary polymer can react with the amine-containing polymer, can contain repeat units that include one or more groups which can react with a portion of the amine-containing polymer.
  • the groups can be selected to react with an amine functionality (primary, secondary, ternary, or quaternary).
  • groups include but are not limited to epoxides, anhydrides (e.g., maleic anhydride), carboxylic acids, and isocyanates.
  • copolymers When copolymers are utilized as a complementary polymer, such copolymers can also contain some repeat units with these reactive groups.
  • the molecular weight of the complementary polymer can be between about 1,000 daltons and about 10,000,000 daltons; or between about 10,000 daltons and about 500,000 daltons.
  • a complementary polymer can be used to enhance the properties of a mixture, or a resulting paper product produced from the mixture.
  • the complementary polymer can be used to provide additional strength to a resulting paper-based product, whether an amine-containing polymer is used to functionalize pulp, filler particles, or both pulp and filler.
  • the complementary polymer can act to bridge components that have been functionalized with the amine-containing polymer. As an example, if only the pulp fibers are functionalized, the polymer bridges different fibers. However, if both the pulp and filler have been functionalized, the filler can also be bound to the pulp for enhancing mechanical properties of the paper making mixture or a resulting paper product.
  • the complementary polymer can contain one or more components that can impart additional or alternative properties to a resulting paper product besides strength enhancement.
  • elastic homopolymers or copolymers can be used to change the resulting paper's stiffness or wear resistance, or hydrophobic homopolymers or copolymers can be used to change the water contact angle (e.g., the tendency to resist water penetration).
  • hydrophobic homopolymers or copolymers can be used to change the water contact angle (e.g., the tendency to resist water penetration).
  • Combinations of various types of complementary polymers can also be used to provide multiple property enhancement (e.g., strength, elasticity, and water resistance).
  • the complementary polymer can be emulsified by the amine-containing polymer. This combination can be mixed with a portion of a pulp furnish, i.e., delivered in one addition versus in sequential steps. In this case, one or a combination of the type of amine-containing polymers discussed previously can be used, along with one or more complementary polymers which are not soluble in water.
  • the complementary polymer can interact nonreactively or react with the amine-containing polymer. Besides being substantially hydrophobic, the complementary polymer can have any of the properties previously disclosed herein.
  • the complementary polymer can either be emulsified using the amine-containing polymer alone (e.g., if it is in liquid form) or dissolved in a water immiscible solvent to form a “water-in-oil” emulsion.
  • This emulsion can then be added to either the fiber and/or filler stream so that the amine-containing polymer can interact with the filler and/or fiber.
  • the miscelle can open up to allow the emulsified polymer to interact or bind between multiple fillers and/or fibers.
  • Some exemplary embodiments are drawn to methods of producing materials such as paper-based materials, which are optionally consistent with one or more of the compositions disclosed herein.
  • One exemplary method includes functionalizing fibers of a pulp using an amine-containing polymer. Filler particles can be combined with the functionalized pulp fibers to produce at least a portion of a paper-forming mixture such as a pulp furnish. A paper-based material can then be produced from the paper-forming mixture. In some instances, it can be advantageous for the method not to substantially functionalize the filler particles, though the pulp components can be functionalized.
  • the method can be practiced as a batch process or in continuous fashion using flowing streams of components.
  • the methods of producing materials functionalize filler particles (e.g., the surface of filler particles) using the amine-containing polymer.
  • Fibers of a pulp can be combined with the functionalized filler particles to produce a portion or the entirety of a paper-making mixture, which can be subsequently used to produce a paper-based material.
  • it can be advantageous in some instances to not substantially functionalize the fibers of the pulp.
  • both the pulp and the filler particles can be functionalized.
  • amine-containing polymers, filler particles, and pulps that can be used with these methods include all the types disclosed in the present application.
  • specific techniques for functionalizing the pulp, filler particle, or both pulp and filler particles can follow the techniques disclosed herein (e.g., addition of coupling agents to aid coupling of an amine-containing polymer to a component).
  • chitosan can be combined with either pulp or filler particles to form a functionalizing mixture.
  • the pH of the mixture can be raised to a level of at least about 6 to cause the chitosan to associate with the pulp fibers or filler particles, thereby functionalizing the component.
  • paper-forming mixtures utilized in the various methods can include any of the other components of mixtures disclosed herein (e.g., complementary polymers).
  • the step of producing a paper-based material from the paper-forming mixture can utilize any set of paper-forming techniques including those known to ones skilled in the art.
  • the paper-forming mixture can be set on a screen to form a sheet.
  • the sheet can be subsequently dried to form the paper product. Modifications of this technique and others to accommodate embodiments disclosed herein are also contemplated by the present application.
  • the complementary polymer in methods that utilize a complementary polymer, can be added to a paper-making mixture before a sheet is formed from the mixture, or after the sheet has been formed (e.g., applied onto the sheet).
  • the complementary polymer when added to the process before sheet formation, it can be of sufficient quantity to produce a desired enhancement in some property (e.g., mechanical properties of the end paper product), but not enough to cause problems with sheet formation.
  • this addition level can be from about 0.01% to about 5.0% (based on sheet dry weight), or between about 0.1% and about 2%.
  • the complementary polymer When the complementary polymer is added after sheet formation, it can be added prior to drying the sheet (e.g., while the sheet is still on the paper machine), or it may be added after drying the sheet (e.g., in a coating or other dry end process).
  • the polymer can be added in solution form which can either be aqueous or non-aqueous. Aqueous solutions can be used when addition is done prior to drying the sheet, but non-aqueous solutions can be advantageous after drying due to energy usage in eliminating the solvent.
  • the complementary polymer When the complementary polymer is reactive, the reaction can occur anytime in the process after introduction of the complementary polymer, i.e., the reaction between the complementary polymer and the amine-containing polymer can occur either immediately after addition or anytime thereafter.
  • the methods described herein can include emulsifying a complementary polymer (e.g., a substantially hydrophobic polymer) with the amine-containing polymer in an aqueous solution.
  • a complementary polymer e.g., a substantially hydrophobic polymer
  • the emulsion formed from the complementary polymer and amine-containing polymer can be added to the pulp fibers, the filler particles, or both to cause the amine-containing polymer to functionalize one or more components.
  • the amine-containing polymer can couple a portion of the pulp and a portion of the filler particles.
  • a 5% pulp slurry was prepared by blending 17.5 g of pine furnish (dry weight) with 32.5 g of birch (dry weight) in 1 L of water. This thick slurry was then diluted to 0.5% by adding 9.5 L of water to the 1 L of thick stock slurry.
  • a 5% pulp slurry was prepared by blending 17.5 g of pine furnish (dry weight) with 32.5 g of birch (dry weight) in 1 L of water. This thick slurry was then diluted to 0.5% by adding 9.5 L of water to the 1 L of thick stock slurry. To this 0.5% slurry, 12.5 mL of a 2.0% CG110 chitosan solution (Primex, Iceland) was slowly added.
  • a 5% pulp slurry was prepared by blending 17.5 g of pine furnish (dry weight) with 32.5 g of birch (dry weight) in 1 L of water. This thick slurry was then diluted to 0.5% by adding 9.5 L of water to the 1 L of thick stock slurry. To this 0.5% slurry, 12.5 mL of a 2.0% CG110 chitosan solution was slowly added. A solution of 0.1 M NaOH was then titrated into the pulp slurry until the pH reached 8.0 (the original pH was approximately 6.5—example 2).
  • a 10% PCC slurry was made by stirring 100 g of PCC into 1 L of water.
  • a 10% PCC slurry was made by stirring 10 g of PCC into 100 mL of water. To this slurry, 2.5 mL of a 2.0% CG110 chitosan solution was slowly added. The high pH of the PCC solution caused the chitosan to precipitate onto the PCC particles. This was verified by taking a sample and attaching a reactive intense blue dye that turned the PCC blue. The dye did not react with PCC that was not functionalized with chitosan.
  • Handsheets were prepared using a handsheet maker, model Mark V Dynamic Handsheet Mold/Paper Chemistry Jar from Paper Chemistry Laboratory Inc. (Larchmont, N.Y.). The appropriate volume of 0.5% pulp slurry (functionalized or unfunctionalized) was combined with the appropriate volume of the 10% filler slurry (functionalized or unfunctionalized). This combined slurry was diluted with water up to 2 L and added to the handsheet maker. The overhead stirrer was then powered on and set to stir at 1100 RPM for 5 seconds, 700 RPM for 5 seconds, 400 RPM for 5 seconds, and then raised out of the slurry. The water was then drained off. The subsequent sheet was then transferred off of the wire and pressed and dried. Each test condition was repeated to make two handsheets for each trial point. Three 1′′ wide strips were then cut out from each handsheet for tensile testing on an Instron Single Column Testing System Model #3343 (Norwood, Mass.). The reported values are the averages of the six strips (three from each handsheet).
  • Two handsheets were produced using the above procedure. In the process, 500 mL of pulp from example 1 was used along with no filler. These were control sheets that had an average max load/width of 9.9 lb/in. When normalized by the basis weight (i.e., the density of each sheet on a mass per unit area basis), the result was 0.11 lb*m 2 /in/g.
  • Two handsheets were produced using the above procedure. In the process, 500 mL of pulp from example 2 was used with no filler. These sheets that had an average max load/width of 10.1 lb/in. When normalized by the basis weight, the result was 0.12 lb*m 2 /in/g.
  • Two handsheets were produced using the above procedure. In the process, 450 mL of pulp from example 3 was used along with 3.0 mL of filler from example 4. The retention of the filler from example 4 with pulp from example 3 was previously tested to be approximately 83%, so these handsheets would be approximately 10% by weight PCC. These 90% fiber/10% PCC sheets had an average max load/width of 10.1 lb/in. When normalized by the basis weight, the result was 0.11 lb*m 2 /in/g; a substantially similar result to the control sample of 100% pulp.
  • Handsheets were created using the above procedures. After drying the handsheet, approximately 6.5 mL of a 0.2% aqueous poly[(isobutylene-alt-maleic acid), ammonium salt)-co-(isobutylene-alt-maleic anhydride] solution was applied to the handsheet. Each test condition was repeated to make two handsheets for each trial point. Three 1′′ wide strips were then cut out of each handsheet for tensile testing on the Instron 3343. The reported values are the averages of the six strips (three from each handsheet).
  • the second polymer addition produced a sheet approximately 35% stronger than the control sheet (example 7).
  • a sheet was produced that was approximately 50% stronger than the sheet with chitosan on pulp (example 8).

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Paper (AREA)

Abstract

Compositions and methods of producing paper-based materials are disclosed. In general, the techniques utilize an amine-containing polymer, such as chitosan, to functionalize one or more components of a mixture used to form materials such as paper-based materials. Such components can include the fibers of a pulp and/or filler particles. In one instance, either the pulp or the filler particles are functionalized, but not both. Such functionalization can improve the qualities of a paper-based material relative to when such functionalization is not utilized. Techniques and compositions are also described to further improve the qualities of a paper material by utilizing a complementary polymer which can couple with the amine-containing polymer.

Description

    RELATED APPLICATIONS
  • This application is a continuation of U.S. application Ser. No. 12/184,308, filed Aug. 1, 2008, which is a continuation of International Application No. PCT/US07/03159, which designated the United States and was filed on Feb. 5, 2007, published in English, which claims the benefit of U.S. Provisional Application No. 60/765,119, filed on Feb. 3, 2006 and U.S. Provisional Application No. 60/864,783, filed on Nov. 7, 2006. The entire teachings of the above applications are incorporated herein by reference.
  • FIELD OF THE INVENTION
  • The technical field of the invention relates to compositions and methods for enhancing the properties of materials such as paper-related products.
  • BACKGROUND OF THE INVENTION
  • Paper manufacturing is an important industrial process, resulting in the production of a vast variety of products. Paper products often times include the use of filler materials, which allow products to be produced more cheaply. The use of fillers, however, can decrease the quality of the product in terms of strength, appearance, and other features. Though additives have been derived for further improving the quality of manufactured paper, a need persists for processes and compositions that further improve the quality of paper. Indeed, the development of additives which result in improved efficiency and lower cost production is desirable.
  • SUMMARY OF THE INVENTION
  • In one aspect, the compositions and methods disclosed herein relate to methods for enhancing the mechanical properties of paper. In particular, these compositions and methods can relate to improving the economics of papermaking, or can enable paper fibers to be used in other applications where presently their use has been limited by their mechanical properties.
  • In another aspect, the techniques disclosed herein can enhance other advantageous properties of paper, such as the hydrophobicity of paper.
  • In other embodiments, the pulp and/or filler to be used in making a paper sheet can be functionalized with an amine-containing polymer. In some embodiments, a complimentary polymer can be added either sequentially or in an emulsion form. When performed sequentially, the complimentary polymer can be added either before or after the formation of a paper sheet.
  • Accordingly, some exemplary embodiments are drawn toward a mixture, which can be used for producing a paper-based material. The mixture can include an aqueous medium, a pulp comprising fibers, filler particles, and an amine-containing polymer. The amine-containing polymer can enhance properties of either the mixture or a paper-based material to be produced from the mixture. The fibers of the pulp can be substantially free of synthetic polymer-based fibers, and/or can have a net negative charge. The filler particles can have an inorganic surface, and can include one or more of calcium carbonate, kaolin, and titanium dioxide. In one related embodiment, the amine-containing polymer can be adapted to functionalize a surface of the filler particles. Optionally in this embodiment, the fibers of the pulp are not substantially functionalized by the amine-containing polymer. In another embodiment, the amine-containing polymer can be substantially coupled to, or functionalize, only one of the pulp and the filler particles.
  • Amine-containing polymers used in some embodiments can include at least one of a homopolymer and a copolymer. The amine-containing polymer can also include at least a polycationic segment such as at least one segment of chitosan, polyalkyleneimine, polyvinyl amine, and polyallyl amine. In a particular embodiment, the amine-containing polymer includes one or more segments of any one of chitosan and branched polyethyleneimine. One or more crosslinking agents (e.g., a silane coupling agent) can be used to couple the amine-containing polymer to a paper component (e.g., filler particles, fibers of pulp, or both). A crosslinking agent can include two or more functionalities for reacting with the amine-containing polymer and/or a paper making component (e.g., filler particles, pulp fibers, or both).
  • Consistent with some embodiments, a complementary polymer can be included for enhancing the properties of a mixture or a paper-based material. Such embodiments can be utilized when both a pulp and filler particles are functionalized by an amine-containing polymer, though only one of the pulp and fillers can be functionalized as well. For example, one exemplary embodiment can be drawn to a mixture including an aqueous medium; a pulp with fibers; an amine-containing polymer for functionalizing a surface of the fibers; and a complementary polymer capable of coupling with the amine-containing polymer.
  • In general, the complementary polymer can be capable of coupling with the amine-containing polymer, either through reaction or some nonreactive interaction (e.g., electrostatic attraction). This can couple a portion of the pulp with a portion of the filler when the amine-containing polymer functionalizes both components. Complementary polymers can be polyanionic, and can be a homopolymer, copolymer, or any combination thereof. The complementary polymer can also include one or more epoxide, anhydride (e.g., maleic anhydride), carboxylic acid, and isocynate groups. Non-limiting examples of complementary polymers include polymers that have at least one polymer segment of pectin, xanthan gum, carboxymethyl cellulose, polyacrylic acid, and polymethacrylic acid. Other types of complementary polymers can have an elastomeric component or a component that increases water resistance of a paper-based material. In a related embodiment, the amine-containing polymer can emulsify the complementary polymer (e.g., a polymer that is substantially insoluble in water).
  • Other exemplary embodiments are drawn to methods of producing a paper-based material. In one embodiment, fibers of a pulp are functionalized using an amine-containing polymer. Filler particles can be combined with the functionalized fibers of the pulp to produce at least a portion of a paper-forming mixture. The mixture can be used to produce a paper-based material. In such an embodiment, the amine-containing polymer optionally does not functionalize the filler particles. In an alternate embodiment, the filler particles are functionalized with the amine-containing polymer. The pulp can be combined with the functionalized filler particles to form the portion of the paper-forming mixture. In the alternate embodiment, the amine-containing polymer optionally does not functionalize the pulp (e.g., the fibers of the pulp). It is also understood that in some of these embodiments, both the filler and the pulp can be functionalized by the amine-containing polymer.
  • These method embodiments can utilize any of the filler particles, pulps, and amine-containing polymers described herein. As well, the methods can include any of the mixtures described herein as well. For instance, the functionalization of fibers of pulp, or filler particles, can be achieved by combining the component with an amine-containing polymer that can include chitosan segments and/or branched polyethyleneimine segments. In one particular instance, the pulp or filler particles can be combined with chitosan to form a functionalizing mixture. The pH of the functionalizing mixture can be raised to at least about 6 to cause the chitosan to associate with the pulp and/or filler particles.
  • Embodiments drawn to methods of producing paper-based materials can also utilize a complementary polymer, the use of which can be consistent with other embodiments disclosed herein. The complementary polymer can be capable of coupling with the amine-containing polymer, through any combination of chemical reaction and nonreactive interaction mechanisms (e.g., electrostatic interactions). The complementary polymer can provide one or more enhanced properties to the produced paper material relative to materials that do not utilize a complementary polymer. Non-limiting examples of enhanced properties include mechanical properties such as strength, stiffness, wear resistance, water resistance (e.g., though increased water contact angle), and elasticity. In some instances, a sheet can be formed using the paper-forming mixture, where the complementary polymer can be added either before or after the sheet is formed. Furthermore, when the complementary polymer is added to a sheet, the addition can occur either before or after the sheet is dried. In other instances, functionalizing either the fibers of a pulp or the filler particles can include emulsifying the complementary polymer with the amine-containing polymer (e.g., a hydrophobic polymer), and adding the emulsion to the component being functionalized.
  • Other embodiments are drawn to paper-based materials produced using any of the compositions or methods disclosed herein.
  • DETAILED DESCRIPTION
  • As utilized in the present application, the term “functionalization” and “functionalize” refer to a change in one or more aspects of the physicochemical nature of an entity. For example, with respect to a particle, functionalization of a particle surface refers to a change in one or more aspects of the particle surface, which result in some physicochemical change in how the particle surface interacts with other entities. Consistent with some embodiments described herein, functionalization of an entity can result in a change in some macroscopic property (e.g., tensile strength) when the functionalized entity is used to produce a product due to the associations of the functionalized entity with other components, or even with other functionalized entities. Functionalization can also alter the types of chemical reactions that an entity can be subjected to relative to when the entity is not functionalized.
  • The term “polymer” refers to a molecule comprising a plurality of repeat units or monomers. A polymer can comprise one or more distinct repeat units. For example, a “copolymer” refers to a polymer having two or more distinct repeat units. Repeat units can be arranged in a variety of manners. For example, a homopolymer refers to a polymer with one type of repeat unit where the repeat units are adjacently connected. In another example, a plurality of different repeat units can be assembled as a copolymer. If A represents one repeat unit and B represents another repeat unit, copolymers can be represented as blocks of joined units (e.g., A-A-A-A-A-A . . . B-B-B-B-B-B . . . ) or interstitially spaced units (e.g., A-B-A-B-A-B . . . or A-A-B-A-A-B-A-A-B . . . ), or randomly arranged units. Of course, these representations can be made with 3 or more types of repeat units as well. In general, polymers (e.g., homopolymers or copolymers) include macromolecules in a broad range of configurations (e.g., cross-linked, linear, and/or branched).
  • The term “segments,” and the phrase “polymer segments,” which can be used interchangeably, refer to a portion of a polymer that includes one or more units. A segment can include one or more types of units (e.g., A-A-A-A or A-B-C-A-C).
  • Some embodiments are directed to compositions and methods for producing materials such as paper-based materials. Such embodiments can utilize an amine-containing polymer, which can be a polycation. The amine-containing polymer can associate with one or more components of a mixture (e.g., a paper-making mixture). Components can include pulp fibers, the surfaces of a particle filler, and other elements or portions of the elements. In general, the association of the amine-containing polymer with any particular component can functionalize that component, potentially increasing the strength, or improving one or more other qualities, of a paper product produced with compositions consistent with such embodiments.
  • Accordingly, some exemplary embodiments are directed to mixtures that can be used to produce various materials, such as paper-based materials. Though such mixtures can include any number of typical components utilized in commercial paper making, some embodiments include a solution medium (e.g., an aqueous solution), a pulp material, and filler particles. The mixtures can include an amine-containing polymer, which can associate and/or interact with one or more components of the mixture. For example, the amine-containing polymer can functionalize the component of the mixture with which the polymer interacts. In one aspect, the amine-containing polymer can functionalize the particle filler component (e.g., the surface of the filler particles), but does not substantially functionalize the pulp. In another aspect, the amine-containing polymer can functionalize the pulp (e.g., the fibers of the pulp), but does not substantially functionalize the filler component. In still another aspect, the amine-containing polymer functionalizes both the filler component and the pulp. Functionalization can and cannot also optionally occur with other components in a selective manner.
  • Functionalization of one or more components of a paper-making mixture with an amine-containing polymer can result in the enhancement of one or more properties of the mixture or a paper product formed from the mixture, relative to the properties when functionalization of the component is absent. For instance, functionalization of one or more components can lead to an enhancement of mechanical properties of a paper product, e.g., tensile strength.
  • With respect to the pulp and the filler particles in a mixture, though some embodiments can utilize functionalization of both components, some particular embodiments only functionalize one of the two components, while leaving the other component substantially unfunctionalized, i.e., either the pulp or the filler particles are functionalized, not both. It has surprisingly been found that in some instances, only functionalizing the pulp or the filler particles, but not both components, can lead to paper products that are stronger, or about as strong, relative to both components being functionalized.
  • The following text describes some features of the components of mixtures consistent with embodiments of the present invention. Unless specifically delineated in particular embodiments, it is understood that one or more of the described features, or specific components, can be utilized with any of the embodiments within the scope of the present application. For instance, any of the specific types of amine-containing polymers can be used in any mixture type (e.g., chitosan or polyalkyleneimines or a combination of the two can be used to functionalize any one or more of pulp, filler particles, and other components of a mixture). It is also understood that features of components can be utilized any combination with the embodiments consistent herein. For instance, in describing the average molecular weight of an amine-containing polymer, it is understood that such average molecular weights can be applied to any described polymer (e.g., homopolymers or copolymers of any particular type of polymer such as branched polyethyleneimine or polyvinylamine). It is further understood that those skilled in the art will appreciate variations and combinations of the described features that are also within the scope of the present disclosure.
  • With respect to various embodiments disclosed herein, an amine-containing polymer can be any homopolymer or copolymer that has at least a portion of its repeat units containing an amine (e.g., quaternary, ternary, secondary or primary). Advantageously, the amine-containing polymer can contain repeat units with primary amines due to the reactivity of the primary amine. In particular embodiments, the amine-containing polymer is a polycation. Polycations can be advantageously utilized, for example, when the components sought to be functionalized have a net negative charge. In such instances, the use of electrostatic interactions with pulp fibers and/or filler can be effective in certain embodiments when the pulp fibers and/or filler have an inherent negative charge that can interact with the polycation.
  • A variety of amine-containing polymers can be utilized with various embodiments that include one or more different types of amine-containing polymers. Amine-containing polymers can be naturally-occurring macromolecules with amine groups such as chitosan. Also, various types of synthetic polymers bearing amine groups such as polyalkyleneimines, polyvinylamine, polyallylamine, and polydiallylamine can be utilized. Of course, copolymers comprising any combination of amine-containing homopolymer units can also be used.
  • In some instances, it can be advantageous to utilize amine-containing polymers that are relatively inexpensive because of the scale and relative costs of paper manufacturing. Chitosan is an aminopolysaccharide typically prepared by deacetylation of chitin (poly-beta(1,4)-N-acetyl-D-glucosamine) obtained from marine organisms such as shrimp, crabs, lobsters, squid, and the like. Accordingly, it can be prepared with relative ease. Branched polyethyleneimine (herein “BPEI”) is an easily manufactured synthetic polymer that is also readily available at moderate cost. Thus, some embodiments utilize chitosan, polyethyleneimine (such as BPEI), or a combination of the two polymers as separate homopolymers or as one or more copolymers. Though many specific instances herein discuss the use of chitosan with particular embodiments and examples, it is understood that such descriptions are merely demonstrative of features of the present invention, and not intended to limit the practice of the present invention.
  • Though the average molecular weight of an amine-containing polymer is not necessarily limited, in some embodiments the average molecular weight of the amine-containing polymer can range from about 1,000 daltons to about 10,000,000 daltons; or from about 10,000 daltons to about 500,000 daltons. Such ranges can advantageously utilize amine-containing polymers which can be large enough to functionalize one or more components effectively, while not being so large as to effect the paper-making process.
  • Measurement of the average molecular weights for any polymer discussed herein can be with respect to a number of bases. For example, can be number averaged, weight averaged, or averaged based on some other weighting factors. As well, the techniques utilized to determine molecular weight can include the range of those known to those skilled in the art. Examples include gel permeation chromatography and light-scattering.
  • For certain amine-containing polymers, the average molecular weight can be difficult to ascertain. Chitosan is an example of such an amine-containing polymer. In such instances, the average molecular weight of the polymer can be defined by some alternative parameter such as viscosity. Accordingly, in some embodiments the chitosan has an average molecular weight defined by a viscosity range between about 10 centipoise and about 800 centipoise. The viscosity can optionally be further defined by a set of conditions, such as being measured for a 1% solution of chitosan in pH 4 (or 0.1M) aqueous acetic acid at 25° C.
  • The pulp utilized in some embodiments disclosed herein can comprise fibers such as cellulose-based fibers, and can also include components typically found in pulps used to make paper products. Accordingly, the fibers of the pulp can have a net negative charge. Such charge can be utilized advantageously in some embodiments to cause electrostatic attraction of an amine-containing polymer that is, or is partially, a polycation. In some embodiments, the fibers of a pulp exclude the presence of synthetic fibers such as polymer-based fibers (e.g., aromatic amide fibers). Thus, some embodiments utilize pulps that include substantially naturally-occurring fibers.
  • Fillers utilized in some embodiments disclosed here can include particulates that are typically utilized as fillers in paper manufacturing applications. For instance, the fillers can have a surface that is, at least partially, substantially inorganic in nature. Thus, non-limiting examples of filler particles can include particles constructed from calcium, carbonate, kaolin, titanium dioxide, and other inorganic materials. Fillers can also be a composite of inorganics. In some embodiments, the surface of the fillers can have a net negative charge, which can tend to attract amine-containing polymers that are polycationic in nature.
  • In some embodiments, functionalization of one or more components (e.g., pulp and/or filler) can be achieved by some type of coupling interaction between an amine-containing polymer and the component. Such coupling can be achieved using either through a coupling agent or through electrostatic interactions that permit the polyamine to self-assemble onto the surface of the component. The use of electrostatic interactions with pulp fibers and filler can be effective in certain embodiments because both pulp fibers and filler have an inherent negative charge that can interact with the polyamine. Coupling agents, such as multifunctional crosslinking agents described herein, can be used to increase the amount of amine-containing polymer that can adhere to a surface, such as a surface of the filler particles.
  • For the compositions and methods disclosed herein, multifunctional crosslinking agents can be used as a coupling agent. Such agents can react with at least one of the amine-containing polymer and the component to be coupled. For example, in some embodiments the multifunctional coupling agent can include a silicon containing coupling agent and at least one of the following functional groups: an epoxy group, a hydroxyl group, a carboxyl group, and/or an isocyano group. In one embodiment, the multifunctional coupling agent is a silane coupling agent. In another embodiment, the coupling agent does not include silicon (e.g., in embodiments in which silicon is not used). In certain embodiments, the multifunctional coupling agent includes an isocyanosilane, for example, a trialkoxy isocyanosilane such as trimethoxy isocyanosilane, triethoxy isocyanosilane, and/or triisopropoxy isocyanosilane. In certain embodiments, the multifunctional coupling agent includes an epoxy siloxane. The multifunctional coupling agent can include triethoxy methacryloxypropyl silane. Other agents can also be employed as would be understood by those of skilled in the art.
  • In some embodiments, functionalization of a paper making component can be achieved without the use of a coupling agent. For instance, the amine-containing polymer can be added directly to a pulp stream, a filler stream, or to both, resulting in the association of the amine-containing polymer and the pulp, filler, or both. If chitosan is used as the amine-containing polymer, the component can be functionalized by precipitating chitosan onto the surface of the component using, for example, a shift in pH. Since chitosan is only soluble in acidic conditions, the polymer can be made to precipitate when the pH is raised by adding a base to the solution after adding chitosan (e.g., to a pH of at least about 6). Accordingly, it can be advantageous to prepare mixtures of one or more components (e.g., one or more of fillers and pulp) with chitosan having a pH close to the precipitation point of the amine-containing polymer to reduce the amount of base needed to induce precipitation and functionalize the component. Thus, the pH of the mixture can be in the range from about 4 to about 8; or from about 5 to about 8; or from about 6 to about 8. In some instances, it can be advantageous to utilize a multivalent acid to enhance the dissolution of chitosan into a pulp furnish or other paper-making mixture. Accordingly, some embodiments can utilize a mixture with one or more multivalent acids; non-limiting examples include citric, tartaric, aldaric (any in the family), oxalic, malonic, malic, succinic, glutaric, and adipic acid.
  • Alternatively, precipitation can occur spontaneously when a chitosan solution is added to a basic environment like a calcium carbonate solution. In some embodiments, the amount of chitosan to be added can be from about 0.01% to about 5.0% (based on weight of the component), or from about 0.1% to about 2%.
  • In some embodiments, a complementary polymer can be added to a paper-making mixture. In general, the complementary polymer can be capable of coupling with an amine-containing polymer (e.g., the complementary polymer can react or nonreactively interact with the amine-containing polymer). Such a complementary polymer can be used to enhance the properties of the mixture, or a resulting paper product produced from the mixture, relative to not using the complementary polymer. The complementary polymer can be utilized when an amine-containing polymer is intended to functionalize pulp (e.g., fibers), filler particles, or both pulp and filler particles, among other paper-making mixture components.
  • In a mixture, the complementary polymer can be coupled with the amine-containing polymer, or can be free but will eventually couple with the amine-containing polymer. As well, the complementary polymer can be added to a process after an amine-containing polymer has functionalized one or more mixture components, or before functionalization has occurred such as in an emulsion technique described herein.
  • Some embodiments can utilize any complementary polymer (e.g., homopolymers, copolymers, and combinations of different polymers) which can interact nonreactively with an amine-containing polymer or which can react with the amine-containing polymer (e.g., reacting with an amine group). If the complementary polymer nonreactively interacts rather than reacts with the amine-containing polymer, the interaction may involve electrostatic forces, hydrogen bonds, or any other secondary interaction forces or association mechanisms. For example, the nonreactive interaction can be an electrostatic interaction when a polyanion is used as a portion or the entirety of the complementary polymer. Accordingly, an appropriate polymer can also be used that includes repeat units with anionic charge. Advantageously, the polyanion can include one or more carboxylic acid groups. Non-limiting examples of suitable polyanions, or polyanion segments, include biopolymers such as pectin, xanthum gum, and carboxymethyl cellulose, and synthetic polymers such as polyacrylic acid or polymethacrylic acid. Other types of complementary polymers, such as polyanions or polymers with polyanionic segments, can also be used consistent with the embodiments disclosed herein.
  • In embodiments when the complementary polymer can react with the amine-containing polymer, the complementary polymer can contain repeat units that include one or more groups which can react with a portion of the amine-containing polymer. In particular embodiments, the groups can be selected to react with an amine functionality (primary, secondary, ternary, or quaternary). Such groups include but are not limited to epoxides, anhydrides (e.g., maleic anhydride), carboxylic acids, and isocyanates. When copolymers are utilized as a complementary polymer, such copolymers can also contain some repeat units with these reactive groups. The molecular weight of the complementary polymer can be between about 1,000 daltons and about 10,000,000 daltons; or between about 10,000 daltons and about 500,000 daltons.
  • As previously mentioned, a complementary polymer can be used to enhance the properties of a mixture, or a resulting paper product produced from the mixture. For example, the complementary polymer can be used to provide additional strength to a resulting paper-based product, whether an amine-containing polymer is used to functionalize pulp, filler particles, or both pulp and filler. Without being bound by theory, it is believed that the complementary polymer can act to bridge components that have been functionalized with the amine-containing polymer. As an example, if only the pulp fibers are functionalized, the polymer bridges different fibers. However, if both the pulp and filler have been functionalized, the filler can also be bound to the pulp for enhancing mechanical properties of the paper making mixture or a resulting paper product.
  • In some embodiments, the complementary polymer can contain one or more components that can impart additional or alternative properties to a resulting paper product besides strength enhancement. As an example, elastic homopolymers or copolymers can be used to change the resulting paper's stiffness or wear resistance, or hydrophobic homopolymers or copolymers can be used to change the water contact angle (e.g., the tendency to resist water penetration). Combinations of various types of complementary polymers can also be used to provide multiple property enhancement (e.g., strength, elasticity, and water resistance).
  • In other embodiments, the complementary polymer can be emulsified by the amine-containing polymer. This combination can be mixed with a portion of a pulp furnish, i.e., delivered in one addition versus in sequential steps. In this case, one or a combination of the type of amine-containing polymers discussed previously can be used, along with one or more complementary polymers which are not soluble in water. The complementary polymer can interact nonreactively or react with the amine-containing polymer. Besides being substantially hydrophobic, the complementary polymer can have any of the properties previously disclosed herein. The complementary polymer can either be emulsified using the amine-containing polymer alone (e.g., if it is in liquid form) or dissolved in a water immiscible solvent to form a “water-in-oil” emulsion. This emulsion can then be added to either the fiber and/or filler stream so that the amine-containing polymer can interact with the filler and/or fiber. For example, upon drying, the miscelle can open up to allow the emulsified polymer to interact or bind between multiple fillers and/or fibers.
  • Some exemplary embodiments are drawn to methods of producing materials such as paper-based materials, which are optionally consistent with one or more of the compositions disclosed herein. One exemplary method includes functionalizing fibers of a pulp using an amine-containing polymer. Filler particles can be combined with the functionalized pulp fibers to produce at least a portion of a paper-forming mixture such as a pulp furnish. A paper-based material can then be produced from the paper-forming mixture. In some instances, it can be advantageous for the method not to substantially functionalize the filler particles, though the pulp components can be functionalized. The method can be practiced as a batch process or in continuous fashion using flowing streams of components.
  • In alternative embodiments, the methods of producing materials functionalize filler particles (e.g., the surface of filler particles) using the amine-containing polymer. Fibers of a pulp can be combined with the functionalized filler particles to produce a portion or the entirety of a paper-making mixture, which can be subsequently used to produce a paper-based material. In this embodiment, it can be advantageous in some instances to not substantially functionalize the fibers of the pulp. In still other embodiments, both the pulp and the filler particles can be functionalized.
  • The types of amine-containing polymers, filler particles, and pulps that can be used with these methods include all the types disclosed in the present application. As well, specific techniques for functionalizing the pulp, filler particle, or both pulp and filler particles can follow the techniques disclosed herein (e.g., addition of coupling agents to aid coupling of an amine-containing polymer to a component). In one particular example, chitosan can be combined with either pulp or filler particles to form a functionalizing mixture. The pH of the mixture can be raised to a level of at least about 6 to cause the chitosan to associate with the pulp fibers or filler particles, thereby functionalizing the component. It is also understood that paper-forming mixtures utilized in the various methods can include any of the other components of mixtures disclosed herein (e.g., complementary polymers).
  • The step of producing a paper-based material from the paper-forming mixture can utilize any set of paper-forming techniques including those known to ones skilled in the art. For example, the paper-forming mixture can be set on a screen to form a sheet. The sheet can be subsequently dried to form the paper product. Modifications of this technique and others to accommodate embodiments disclosed herein are also contemplated by the present application.
  • For example, in methods that utilize a complementary polymer, the complementary polymer can be added to a paper-making mixture before a sheet is formed from the mixture, or after the sheet has been formed (e.g., applied onto the sheet). When the complementary polymer is added to the process before sheet formation, it can be of sufficient quantity to produce a desired enhancement in some property (e.g., mechanical properties of the end paper product), but not enough to cause problems with sheet formation. In some embodiments, this addition level can be from about 0.01% to about 5.0% (based on sheet dry weight), or between about 0.1% and about 2%.
  • When the complementary polymer is added after sheet formation, it can be added prior to drying the sheet (e.g., while the sheet is still on the paper machine), or it may be added after drying the sheet (e.g., in a coating or other dry end process). The polymer can be added in solution form which can either be aqueous or non-aqueous. Aqueous solutions can be used when addition is done prior to drying the sheet, but non-aqueous solutions can be advantageous after drying due to energy usage in eliminating the solvent. When the complementary polymer is reactive, the reaction can occur anytime in the process after introduction of the complementary polymer, i.e., the reaction between the complementary polymer and the amine-containing polymer can occur either immediately after addition or anytime thereafter.
  • In alternative embodiments connected with the use of a complementary polymer, the methods described herein can include emulsifying a complementary polymer (e.g., a substantially hydrophobic polymer) with the amine-containing polymer in an aqueous solution. The emulsion formed from the complementary polymer and amine-containing polymer can be added to the pulp fibers, the filler particles, or both to cause the amine-containing polymer to functionalize one or more components. In instances where both pulp fibers and filler particles are functionalized, the amine-containing polymer can couple a portion of the pulp and a portion of the filler particles.
  • Other embodiments are drawn to paper-based materials that can be produced from any of the mixtures or methods described in the present application.
  • EXAMPLES
  • The following examples are provided to illustrate some aspects of the present application. The examples, however are not meant to limit the practice of any embodiment of the invention.
  • Example 1 Control Pulp Synthesis
  • A 5% pulp slurry was prepared by blending 17.5 g of pine furnish (dry weight) with 32.5 g of birch (dry weight) in 1 L of water. This thick slurry was then diluted to 0.5% by adding 9.5 L of water to the 1 L of thick stock slurry.
  • Example 2 Chitosan on Pulp (No Base Addition)
  • A 5% pulp slurry was prepared by blending 17.5 g of pine furnish (dry weight) with 32.5 g of birch (dry weight) in 1 L of water. This thick slurry was then diluted to 0.5% by adding 9.5 L of water to the 1 L of thick stock slurry. To this 0.5% slurry, 12.5 mL of a 2.0% CG110 chitosan solution (Primex, Iceland) was slowly added.
  • Example 3 Chitosan on Pulp (With Addition of NaOH)
  • A 5% pulp slurry was prepared by blending 17.5 g of pine furnish (dry weight) with 32.5 g of birch (dry weight) in 1 L of water. This thick slurry was then diluted to 0.5% by adding 9.5 L of water to the 1 L of thick stock slurry. To this 0.5% slurry, 12.5 mL of a 2.0% CG110 chitosan solution was slowly added. A solution of 0.1 M NaOH was then titrated into the pulp slurry until the pH reached 8.0 (the original pH was approximately 6.5—example 2).
  • Example 4 Control Precipitated Calcium Carbonate (PCC)
  • A 10% PCC slurry was made by stirring 100 g of PCC into 1 L of water.
  • Example 5 Chitosan Coated PCC
  • A 10% PCC slurry was made by stirring 10 g of PCC into 100 mL of water. To this slurry, 2.5 mL of a 2.0% CG110 chitosan solution was slowly added. The high pH of the PCC solution caused the chitosan to precipitate onto the PCC particles. This was verified by taking a sample and attaching a reactive intense blue dye that turned the PCC blue. The dye did not react with PCC that was not functionalized with chitosan.
  • Example 6 Handsheet Preparation
  • Handsheets were prepared using a handsheet maker, model Mark V Dynamic Handsheet Mold/Paper Chemistry Jar from Paper Chemistry Laboratory Inc. (Larchmont, N.Y.). The appropriate volume of 0.5% pulp slurry (functionalized or unfunctionalized) was combined with the appropriate volume of the 10% filler slurry (functionalized or unfunctionalized). This combined slurry was diluted with water up to 2 L and added to the handsheet maker. The overhead stirrer was then powered on and set to stir at 1100 RPM for 5 seconds, 700 RPM for 5 seconds, 400 RPM for 5 seconds, and then raised out of the slurry. The water was then drained off. The subsequent sheet was then transferred off of the wire and pressed and dried. Each test condition was repeated to make two handsheets for each trial point. Three 1″ wide strips were then cut out from each handsheet for tensile testing on an Instron Single Column Testing System Model #3343 (Norwood, Mass.). The reported values are the averages of the six strips (three from each handsheet).
  • Example 7 Control 100% Pulp
  • Two handsheets were produced using the above procedure. In the process, 500 mL of pulp from example 1 was used along with no filler. These were control sheets that had an average max load/width of 9.9 lb/in. When normalized by the basis weight (i.e., the density of each sheet on a mass per unit area basis), the result was 0.11 lb*m2/in/g.
  • Example 8 100% Pulp (w/Chitosan, No Base)
  • Two handsheets were produced using the above procedure. In the process, 500 mL of pulp from example 2 was used with no filler. These sheets that had an average max load/width of 10.1 lb/in. When normalized by the basis weight, the result was 0.12 lb*m2/in/g.
  • Example 9 Control 90% Pulp/10% PCC
  • Two handsheets were produced using the above procedure. In the process, 450 mL of pulp from example 1 was used along with 12.5 mL of filler from example 4. The retention of the filler from example 4 with pulp from example 1 was previously tested to be approximately 20%, so these handsheets would be approximately 10% by weight PCC. These 90% fiber/10% PCC sheets had an average max load/width of 5.9 lb/in. When normalized by the basis weight, the result was 0.068 lb*m2/in/g.
  • Example 10 90% Pulp (With Chitosan, No Base)/10% PCC
  • Two handsheets were produced using the above procedure. In the process, 450 mL of pulp from example 2 was used along with 3.0 mL of filler from example 4. The retention of the filler from example 4 with pulp from example 2 was previously tested to be approximately 83%, so these handsheets would be approximately 10% by weight PCC. These 90% fiber/10% PCC sheets had an average max load/width of 9.1 lb/in. When normalized by the basis weight, the result was 0.095 lb*m2/in/g.
  • Example 11 90% Pulp (With Chitosan, NaOH Added)/10% PCC
  • Two handsheets were produced using the above procedure. In the process, 450 mL of pulp from example 3 was used along with 3.0 mL of filler from example 4. The retention of the filler from example 4 with pulp from example 3 was previously tested to be approximately 83%, so these handsheets would be approximately 10% by weight PCC. These 90% fiber/10% PCC sheets had an average max load/width of 10.1 lb/in. When normalized by the basis weight, the result was 0.11 lb*m2/in/g; a substantially similar result to the control sample of 100% pulp.
  • Example 12 90% Pulp/10% PCC (With Chitosan)
  • Two handsheets were produced using the above procedure. In the process, 450 mL of pulp from example 1 was used along with 2.5 mL of filler from example 5. The retention of the filler from example 5 with pulp from example 1 was previously tested to be approximately 99%, so these handsheets would be approximately 10% by weight PCC. These 90% fiber/10% PCC sheets had an average max load/width of 8.2 lb/in. When normalized by the basis weight, the result was 0.087 lb*m2/in/g.
  • Example 13 90% Pulp (With Chitosan, NaOH Added)/10% PCC (With Chitosan)
  • Two handsheets were produced using the above procedure. In the process, 450 mL of pulp from example 3 was used along with 2.5 mL of filler from example 5. The retention of the filler from example 5 with pulp from example 1 was previously tested to be approximately 99%, so these handsheets would be approximately 10% by weight PCC. These 90% fiber/10% PCC sheets had an average max load/width of 7.2 lb/in. When normalized by the basis weight, the result was 0.080 lb*m2/in/g. Accordingly, example 13 shows that functionalizing the pulp and PCC with chitosan unexpectedly results in a sheet that is less strong than just functionalizing the pulp (example 11) or just functionalizing the PCC (example 12).
  • Example 14 Addition of a Complementary Polymer
  • Handsheets were created using the above procedures. After drying the handsheet, approximately 6.5 mL of a 0.2% aqueous poly[(isobutylene-alt-maleic acid), ammonium salt)-co-(isobutylene-alt-maleic anhydride] solution was applied to the handsheet. Each test condition was repeated to make two handsheets for each trial point. Three 1″ wide strips were then cut out of each handsheet for tensile testing on the Instron 3343. The reported values are the averages of the six strips (three from each handsheet).
  • Example 14a Poly[(isobutylene-alt-maleic acid), ammonium salt)-co-(isobutylene-alt-maleic anhydride] Added to 100% Pulp
  • Two handsheets were made using the procedure described in example 7 (100% pulp). Then, the sheets were treated with the Poly[(isobutylene-alt-maleic acid), ammonium salt)-co-(isobutylene-alt-maleic anhydride] solution using the above procedure. These sheets had an average max load/width of 13.2 lb/in. When normalized by the basis weight, the result was 0.14 lb*m2/in/g.
  • Example 14b Poly[(isobutylene-alt-maleic acid), ammonium salt)-co-(isobutylene-alt-maleic anhydride] Added to 100% Pulp with Chitosan
  • Two handsheets were made using the procedure described in example 8 (100% pulp with chitosan). Then, the sheets were treated with the Poly[(isobutylene-alt-maleic acid), ammonium salt)-co-(isobutylene-alt-maleic anhydride] solution using the above procedure. These sheets had an average max load/width of 14.2 lb/in. When normalized by the basis weight, the result was 0.16 lb*m2/in/g.
  • In example 14a, the second polymer addition produced a sheet approximately 35% stronger than the control sheet (example 7). In example 14b, a sheet was produced that was approximately 50% stronger than the sheet with chitosan on pulp (example 8).
  • While the present invention has been described in terms of specific methods, structures, and devices it is understood that variations and modifications will occur to those skilled in the art upon consideration of the present application. As well, the features illustrated or described in connection with one embodiment may be combined with the features of other embodiments. Such modifications and variations are intended to be included within the scope of the present invention. Those skilled in the art will appreciate, or be able to ascertain using no more than routine experimentation, further features and advantages of the invention based on the above-described embodiments. Accordingly, the invention is not to be limited by what has been particularly shown and described, except as indicated by the appended claims. All publications and references are herein expressly incorporated by reference in their entirety.

Claims (44)

1-64. (canceled)
65. A method of producing a paper-based material, comprising:
functionalizing fibers of a pulp using an amine-containing polymer;
combining filler particles with the functionalized fibers of the pulp to produce at least a portion of a paper-forming mixture; and
producing the paper-based material from the paper-forming mixture.
66. The method of claim 65, wherein the amine-containing polymer does not functionalize the filler particles.
67. The method of claim 65, wherein the pulp is substantially free of synthetic polymer-based fibers.
68. The method of claim 65, wherein the step of functionalizing fibers includes combining the pulp with a polymer comprising at least one of chitosan segments and branched polyethyleneimine segments.
69. The method of claim 68, wherein the step of combining the pulp with the polymer includes:
combining the pulp with chitosan to form a functionalizing mixture; and
raising the pH of the functionalizing mixture to at least about 6 to cause the chitosan to associate with a surface of fibers of the pulp.
70. The method of claim 65, wherein the step of functionalizing fibers includes adding a crosslinking agent to couple the amine-containing polymer to the fibers of the pulp.
71. The method of claim 65, further comprising:
adding a complementary polymer to functionalized fibers of the pulp, the complementary polymer capable of coupling with the amine-containing polymer.
72. The method of claim 71, wherein the step of adding the complementary polymer includes coupling the complementary polymer to the amine-containing polymer without using a chemical reaction.
73. The method of claim 71, wherein the step of adding the complementary polymer includes coupling the complementary polymer to the amine-containing polymer using a chemical reaction.
74. The method of claim 71, wherein the step of adding the complementary polymer includes increasing strength of the paper-based material formed by the method.
75. The method of claim 71, wherein the step of adding the complementary polymer includes altering stiffness of the paper-based material formed by the method.
76. The method of claim 71, wherein the step of adding the complementary polymer includes increasing wear resistance of the paper-based material formed by the method.
77. The method of claim 71, wherein the step of adding the complementary polymer includes increasing water-resistance of the paper-based material formed by the method.
78. The method of claim 77, wherein the step of adding the complementary polymer includes increasing water-contact angle of the paper-based material formed by the method.
79. The method of claim 71, wherein the step of producing the paper-based material includes forming a sheet with the paper-forming mixture, and further wherein the step of adding the complementary polymer is performed before the step of forming the sheet.
80. The method of claim 71, wherein the step of producing the paper-based material includes forming a sheet with the paper-forming mixture, and further wherein the step of adding the complementary polymer is performed after the step of forming the sheet.
81. The method of claim 80, wherein the step of producing the paper-based material further includes drying the sheet, and further wherein the step of adding the complementary polymer is performed before drying the sheet.
82. The method of claim 80, wherein the step of producing the paper-based material further includes drying the sheet, and further wherein the step of adding the complementary polymer is performed after drying the sheet.
83. The method of claim 65, wherein the step of functionalizing fibers comprises:
emulsifiying a complementary polymer with the amine-containing polymer in an aqueous solution; and
adding the emulsion to the fibers of the pulp to cause attraction between the amine-containing polymer and the fibers of the pulp.
84. The method of claim 83, wherein the complementary polymer is a hydrophobic polymer.
85. A method of producing a paper-based material, comprising:
functionalizing a surface of filler particles using an amine-containing polymer;
combining fibers of a pulp with the functionalized filler particles to produce at least a portion of a paper-forming mixture; and
producing the paper-based material from the paper-forming mixture.
86. The method of claim 85, wherein the amine-containing polymer does not functionalize the fibers of the pulp.
87. The method of claim 85, wherein the pulp is substantially free of synthetic polymer-based fibers.
88. The method of claim 85, wherein the step of functionalizing the surface includes combining the filler particles with a polymer comprising at least one of chitosan segments and branched polyethyleneimine segments.
89. The method of claim 88, wherein the step of combining the filler particles with the polymer includes:
combining the filler particles with chitosan to form a functionalizing mixture; and
raising the pH of the functionalizing mixture to at least about 6 to cause the chitosan to associate with the surface of the filler particles.
90. The method of claim 85, wherein the surface of the filler particles is an inorganic surface.
91. The method of claim 85, wherein the step of functionalizing the surface includes adding a crosslinking agent to couple the amine-containing polymer to the surface of the filler particles.
92. The method of claim 85, further comprising:
adding a complementary polymer to the functionalized filler particles, the complementary polymer capable of coupling with the amine-containing polymer.
93. The method of claim 92, wherein the step of adding the complementary polymer includes coupling the complementary polymer to the amine-containing polymer without using a chemical reaction.
94. The method of claim 92, wherein the step of adding the complementary polymer includes coupling the complementary polymer to the amine-containing polymer using a chemical reaction.
95. The method of claim 92, wherein the step of adding the complementary polymer includes increasing strength of the paper-based material formed by the method.
96. The method of claim 92, wherein the step of adding the complementary polymer includes altering stiffness of the paper-based material formed by the method.
97. The method of claim 92, wherein the step of adding the complementary polymer includes increasing wear resistance of the paper-based material formed by the method.
98. The method of claim 92, wherein the step of adding the complementary polymer includes increasing water-resistance of the paper-based material formed by the method.
99. The method of claim 98, wherein the step of adding the complementary polymer includes increasing water-contact angle of the paper-based material formed by the method.
100. The method of claim 92, wherein the step of producing the paper-based material includes forming a sheet with the paper-forming mixture, and further wherein the step of adding the complementary polymer is performed before the step of forming the sheet.
101. The method of claim 92, wherein the step of producing the paper-based material includes forming a sheet with the paper-forming mixture, and further wherein the step of adding the complementary polymer is performed after the step of forming the sheet.
102. The method of claim 101, wherein the step of producing the paper-based material further includes drying the sheet, and further wherein the step of adding the complementary polymer is performed before drying the sheet.
103. The method of claim 101, wherein the step of producing the paper-based material further includes drying the sheet, and further wherein the step of adding the complementary polymer is performed after drying the sheet.
104. The method of claim 85, wherein the step of functionalizing fibers comprises:
emulsifying a complementary polymer with the amine-containing polymer in an aqueous solution;
adding the emulsion to the filler particles to cause attraction between the amine-containing polymer and the filler particles.
105. The method of claim 104, wherein the complementary polymer is a hydrophobic polymer.
106. The method of claim 92, wherein at least a portion of the fibers of the pulp are also functionalized by the amine-containing polymer.
107. The method of claim 106, wherein at least a portion of the complementary polymer couples a portion of the pulp and a portion of the filler particles.
US13/369,392 2006-02-03 2012-02-09 Functionalization of paper components Abandoned US20120285644A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US13/369,392 US20120285644A1 (en) 2006-02-03 2012-02-09 Functionalization of paper components

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US76511906P 2006-02-03 2006-02-03
US86478306P 2006-11-07 2006-11-07
PCT/US2007/003159 WO2007092450A2 (en) 2006-02-03 2007-02-05 Functionalization of paper components
US12/184,308 US8123906B2 (en) 2006-02-03 2008-08-01 Functionalization of paper components
US13/369,392 US20120285644A1 (en) 2006-02-03 2012-02-09 Functionalization of paper components

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US12/184,308 Continuation US8123906B2 (en) 2006-02-03 2008-08-01 Functionalization of paper components

Publications (1)

Publication Number Publication Date
US20120285644A1 true US20120285644A1 (en) 2012-11-15

Family

ID=38345746

Family Applications (2)

Application Number Title Priority Date Filing Date
US12/184,308 Expired - Fee Related US8123906B2 (en) 2006-02-03 2008-08-01 Functionalization of paper components
US13/369,392 Abandoned US20120285644A1 (en) 2006-02-03 2012-02-09 Functionalization of paper components

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US12/184,308 Expired - Fee Related US8123906B2 (en) 2006-02-03 2008-08-01 Functionalization of paper components

Country Status (4)

Country Link
US (2) US8123906B2 (en)
EP (1) EP1984564A4 (en)
CA (1) CA2641309A1 (en)
WO (1) WO2007092450A2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120152476A1 (en) * 2009-08-12 2012-06-21 Nanopaper, Llc High strength paper
US9587353B2 (en) 2012-06-15 2017-03-07 Nanopaper, Llc Additives for papermaking
US20240052571A1 (en) * 2022-08-03 2024-02-15 World Centric Moisture/oil resistant composite materials

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1928404A2 (en) * 2005-08-09 2008-06-11 Soane Labs, LLC Hair hold formulations
US20090165976A1 (en) * 2006-02-03 2009-07-02 Nanopaper, Llc Expansion agents for paper-based materials
CA2641309A1 (en) 2006-02-03 2007-08-16 Nanopaper Llc Functionalization of paper components with an amine-containing polymer
US7820563B2 (en) * 2006-10-23 2010-10-26 Hawaii Nanosciences, Llc Compositions and methods for imparting oil repellency and/or water repellency
WO2009018327A2 (en) * 2007-07-30 2009-02-05 Soane Labs, Llc Ultraphobic compositions and methods of use
CA2738087A1 (en) * 2008-09-22 2010-03-25 Patrick D. Kincaid Fibrous products and methods of manufacture
WO2011072349A1 (en) * 2009-12-18 2011-06-23 Universidade Estadual De Campinas - Unicamp Biodegradable sensor containing h2s indicators and method for producing same
JP5649632B2 (en) 2012-05-02 2015-01-07 山田 菊夫 Manufacturing method of water-disintegrating paper
WO2014052300A1 (en) * 2012-09-26 2014-04-03 Earth Renewable Technologies Extrudable composition derived from renewable resources
US10441978B2 (en) 2014-05-30 2019-10-15 Kikuo Yamada Fiber sheet
CN107604739B (en) * 2017-09-26 2019-06-07 江南大学 A kind of filtering preparation method of cotton stalk bark fiber and the compound nonwoven fabric of chitosan
CN111608014B (en) * 2020-04-13 2022-07-15 仙鹤股份有限公司 High-performance low-quantitative dictionary paper and preparation method thereof

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5061346A (en) * 1988-09-02 1991-10-29 Betz Paperchem, Inc. Papermaking using cationic starch and carboxymethyl cellulose or its additionally substituted derivatives
US5200036A (en) * 1990-04-30 1993-04-06 The Procter & Gamble Company Paper with polycationic latex strength agent
USRE35151E (en) * 1991-02-20 1996-01-30 Fuji Spinning Company, Limited Modified cellulose regenerated fiber comprising chitosan particles
US5807636A (en) * 1994-12-16 1998-09-15 Advanced Surface Technology Durable hydrophilic surface coatings
US5827610A (en) * 1997-01-10 1998-10-27 E. I. Du Pont De Nemours And Company Chitosan-coated pulp, a paper using the pulp, and a process for making them
US20020088579A1 (en) * 1998-11-23 2002-07-11 Sven Forsberg Method of producing a particle or group of particles having a coating of polymers interacting with each other
US20030134120A1 (en) * 2001-12-24 2003-07-17 Ibeks Technologies Co., Ltd. Natural fiber coated with chitosan and a method for producing the same
US6767553B2 (en) * 2001-12-18 2004-07-27 Kimberly-Clark Worldwide, Inc. Natural fibers treated with acidic odor control/binder systems
US6936136B2 (en) * 2002-12-31 2005-08-30 Kimberly-Clark Worldwide, Inc. Amino-functionalized pulp fibers
US6939443B2 (en) * 2002-06-19 2005-09-06 Lanxess Corporation Anionic functional promoter and charge control agent

Family Cites Families (92)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3049469A (en) * 1957-11-07 1962-08-14 Hercules Powder Co Ltd Application of coating or impregnating materials to fibrous material
US2601597A (en) * 1946-09-06 1952-06-24 American Cyanamid Co Application of dispersed coating materials to cellulosic fibers
US3545909A (en) 1958-06-26 1970-12-08 Union Carbide Corp Polyaminoalkylsilanes color fixation and articles so colored
GB948163A (en) 1960-10-31 1964-01-29 Ici Ltd Improvements in or relating to fillers, pigments and like materials
US3567680A (en) 1968-05-03 1971-03-02 Huber Corp J M Surface modified pigments and methods for producing same and elastomers containing same
US3902958A (en) * 1974-01-30 1975-09-02 Nalco Chemical Co Method of making improved paper and paper products
DE2429762C2 (en) 1974-06-21 1984-08-30 Merck Patent Gmbh, 6100 Darmstadt Dye-containing luster pigments
JPS51105406A (en) * 1975-02-12 1976-09-18 Mitsubishi Paper Mills Ltd Senishiito * b * noseizoho
US4199142A (en) 1976-04-30 1980-04-22 Michael Ebert Toys and games using super-hydrophobic surfaces
US4142724A (en) 1976-04-30 1979-03-06 Michael Ebert Water maze game with super-hydrophobic surface
US4151154A (en) 1976-09-29 1979-04-24 Union Carbide Corporation Silicon treated surfaces
US4102738A (en) 1977-01-17 1978-07-25 American Cyanamid Company Use of chitosan in corrugating medium
DE2739845A1 (en) 1977-09-03 1979-03-15 Dynamit Nobel Ag Process for the production of colored pigments
DE2812635A1 (en) 1978-03-22 1979-09-27 Bayer Ag HETEROCYCLIC COMPOUNDS
DE2935720A1 (en) 1979-09-04 1981-03-12 Bayer Ag, 5090 Leverkusen AZO DYES, INTERMEDIATE PRODUCTS AND METHOD FOR THE PRODUCTION THEREOF AND METHOD FOR PIGMENTING ORGANIC MATERIAL.
US4309480A (en) 1980-02-28 1982-01-05 The Mearl Corporation Iron blue nacreous pigments
US4402703A (en) 1982-01-06 1983-09-06 Albany International Corp. Bleed resistant colored crepe paper and the method of its preparation
US4398915A (en) 1982-01-06 1983-08-16 Albany International Corp. Bleed resistant colored cellulosics and the method of their preparation
US4543128A (en) 1982-04-05 1985-09-24 Sandoz Ltd. Fillers dyed with polycationic dyestuffs useful for coloring paper and non-woven fabrics
IT1173680B (en) 1983-10-28 1987-06-24 Montedison Spa DYES AND PIGMENTS PERYLENE COMPOSITE TETRACARBOSSIL DIIMIDIC SILANIC
US4566908A (en) 1984-02-24 1986-01-28 Mita Industrial Company, Limited Azoic pigments having a silica core
DE3412730A1 (en) 1984-04-05 1985-10-17 Hoechst Ag, 6230 Frankfurt DISAZO CONNECTIONS, METHOD FOR THEIR PRODUCTION AND THEIR USE
GB8521646D0 (en) 1985-08-30 1985-10-02 English Clays Lovering Pochin Inorganic fillers
GB8531558D0 (en) 1985-12-21 1986-02-05 Wiggins Teape Group Ltd Loaded paper
JPS62226809A (en) 1986-03-27 1987-10-05 Olympus Optical Co Ltd Silica substance
JPH0678213B2 (en) 1986-05-15 1994-10-05 ライオン株式会社 Hair cosmetics
US4755229A (en) 1987-02-09 1988-07-05 The Mearl Corporation Colored micaceous pigments
JPH0697333B2 (en) 1987-03-18 1994-11-30 コニカ株式会社 Method for preventing photo-fading of organic coloring substances
JPS63316717A (en) 1987-06-18 1988-12-26 Lion Corp Permanent wave agent
FI78924C (en) 1988-01-22 1989-10-10 Kemira Oy Dye or color pigment containing pearl pigment and a process for its preparation
US5378574A (en) 1988-08-17 1995-01-03 Xerox Corporation Inks and liquid developers containing colored silica particles
US5338406A (en) * 1988-10-03 1994-08-16 Hercules Incorporated Dry strength additive for paper
US4968351A (en) 1988-11-02 1990-11-06 The Mearl Corporation Nacreous pigments colored by adsorbed dyes
US5147507A (en) 1990-03-08 1992-09-15 Pfizer Inc. Cationic polymer-modified filler material, process for its prepartion and method of its use in papermaking
DE4007535A1 (en) 1990-03-09 1991-09-12 Hoechst Ag WATER-INSOLUBLE AZO PAINTS, THEIR PRODUCTION AND USE
JPH0628890B2 (en) 1990-08-22 1994-04-20 工業技術院長 Method for producing film or sheet composed of natural polysaccharides
US5344489A (en) 1991-11-15 1994-09-06 Manfred R. Kuehnle Synthetic, monodispersed color pigments for the coloration of media such as printing inks, and method and apparatus for making same
US6696585B1 (en) 1993-04-13 2004-02-24 Southwest Research Institute Functionalized nanoparticles
GB9310438D0 (en) 1993-05-20 1993-07-07 Ecc Int Ltd Pigmenting fillers for polymeric compositions
US5427652A (en) * 1994-02-04 1995-06-27 The Mead Corporation Repulpable wet strength paper
US5532059A (en) 1994-09-29 1996-07-02 E. I. Du Pont De Nemours And Company Poly(p-phenylene terephthalamide) pulp
US6228217B1 (en) * 1995-01-13 2001-05-08 Hercules Incorporated Strength of paper made from pulp containing surface active, carboxyl compounds
US5656257A (en) 1995-04-28 1997-08-12 Electronics Hair Styling, Inc. Shampoo and conditioning composition
EP0812956A4 (en) 1995-12-28 2000-05-17 Oji Paper Co High performance paper and process for producing the same
DE19821665A1 (en) 1997-05-28 1998-12-03 Basf Ag Composite pigment with good fastness to colour bleeding
US6599631B2 (en) 2001-01-26 2003-07-29 Nanogram Corporation Polymer-inorganic particle composites
US5958180A (en) 1997-09-23 1999-09-28 International Paper Company Method for increasing the strength of a paper or paperboard product
GB9726807D0 (en) 1997-12-18 1998-02-18 Mupor Ltd Hydrophobic/Oleophobic surfaces and a method of manufacture
CA2324949A1 (en) 1998-03-24 1999-09-30 Avantgarb, Llc Modified textile and other materials and methods for their preparation
US6261679B1 (en) 1998-05-22 2001-07-17 Kimberly-Clark Worldwide, Inc. Fibrous absorbent material and methods of making the same
US6649222B1 (en) 1998-09-07 2003-11-18 The Procter & Gamble Company Modulated plasma glow discharge treatments for making superhydrophobic substrates
US20010044477A1 (en) * 1998-12-10 2001-11-22 Soane David S. Expandable polymeric microspheres, their method of production, and uses and products thereof
US6096469A (en) 1999-05-18 2000-08-01 3M Innovative Properties Company Ink receptor media suitable for inkjet printing
WO2001006054A1 (en) 1999-07-19 2001-01-25 Avantgarb, Llc Nanoparticle-based permanent treatments for textiles
US6780497B1 (en) 1999-08-05 2004-08-24 Gore Enterprise Holdings, Inc. Surface modified expanded polytetrafluoroethylene devices and methods of producing the same
US6368456B1 (en) * 1999-08-17 2002-04-09 National Starch And Chemical Investment Holding Corporation Method of making paper from aldehyde modified cellulose pulp with selected additives
US6812276B2 (en) * 1999-12-01 2004-11-02 General Electric Company Poly(arylene ether)-containing thermoset composition, method for the preparation thereof, and articles derived therefrom
US6497732B1 (en) 2000-02-28 2002-12-24 Nano-Tex, Llc Fiber-reactive polymeric dyes
US6497733B1 (en) 2000-04-03 2002-12-24 Nano-Tex, Llc Dye fixatives
US6635702B1 (en) 2000-04-11 2003-10-21 Noveon Ip Holdings Corp. Stable aqueous surfactant compositions
AU2001253417B2 (en) 2000-04-14 2006-06-15 Soane Laboratories, Llc. Nanoscopic hair care products
CA2420552A1 (en) 2000-10-02 2002-04-11 Kimberly-Clark Worldwide, Inc. Nanoparticle based inks and methods of making the same
US20020068139A1 (en) 2000-12-04 2002-06-06 Polak Brent T. Foamed starch structures & methods for making them
EP1358282A1 (en) 2000-12-15 2003-11-05 Ucb S.A. Surface functionalization of pigments and/or dyes for radiation curable ink printing and coating applications
EP1383470B8 (en) 2001-04-30 2009-09-09 Unilever PLC Hair treatment compositions
EP1412580B1 (en) 2001-05-18 2008-11-12 Sun Chemical Corporation Method of coloring cellulosic materials using a cationic pigment dispersion
FR2831178B1 (en) 2001-10-22 2006-04-14 Rhodia Chimie Sa PIGMENT COMPOSITIONS BASED ON SILICA
FR2831179B1 (en) 2001-10-22 2005-04-15 Rhodia Chimie Sa PROCESS FOR THE AQUEOUS PREPARATION OF SILICA-BASED PIGMENT COMPOSITIONS
FR2831176A1 (en) 2001-10-22 2003-04-25 Rhodia Elect & Catalysis Pigment composition, e.g. useful for coloration of plastics, paints, rubber, ceramics, glazes, paper, inks and cosmetics, comprises a dye covalently bound to rare earth metal sulfide particles through a coupling agent
US6824650B2 (en) 2001-12-18 2004-11-30 Kimberly-Clark Worldwide, Inc. Fibrous materials treated with a polyvinylamine polymer
AU2003218571B2 (en) 2002-04-09 2007-11-29 Fpinnovations Swollen starch-latex compositions for use in papermaking
US6699319B2 (en) 2002-05-06 2004-03-02 Cabot Corporation Process for preparing modified pigments
JP2003322992A (en) 2002-05-08 2003-11-14 Fuji Photo Film Co Ltd Electrophotographic image receiving sheet
US6955844B2 (en) 2002-05-24 2005-10-18 Innovative Construction And Building Materials Construction materials containing surface modified fibers
US20040110883A1 (en) 2002-10-18 2004-06-10 Pakan Dwight J. Coloration of paper by binding colorants in a surface application
WO2004041942A1 (en) 2002-10-24 2004-05-21 Rhodia Electronics And Catalysis Colloidal dispersion and cerium or cerium and titanium, zirconium, aluminium or rare earth coloured powder, method for preparing same and use thereof
US6884479B2 (en) 2002-12-16 2005-04-26 Eastman Kodak Company Ink jet recording element
US6796649B2 (en) 2002-12-16 2004-09-28 Eastman Kodak Company Ink jet printing method
FR2849049B1 (en) 2002-12-20 2005-06-03 COLORED PIGMENT COMPOSITIONS BASED ON SILICA.
FR2848845B1 (en) 2002-12-20 2005-05-06 ANTI-UV COMPOSITION BASED ON MINERAL PARTICLES AND THEIR PREPARATION
US6923216B2 (en) 2003-04-15 2005-08-02 Entegris, Inc. Microfluidic device with ultraphobic surfaces
US6852390B2 (en) 2003-04-15 2005-02-08 Entegris, Inc. Ultraphobic surface for high pressure liquids
US20050038498A1 (en) 2003-04-17 2005-02-17 Nanosys, Inc. Medical device applications of nanostructured surfaces
JP4871726B2 (en) 2003-04-28 2012-02-08 ナノシス・インク. Super lyophobic surface, its preparation and use
US20050084456A1 (en) 2003-10-21 2005-04-21 Liping Tang Functionalized particles
JP4577481B2 (en) 2003-12-22 2010-11-10 日清紡ホールディングス株式会社 Inorganic-organic composite functional composition
FR2872412B1 (en) 2004-06-30 2007-07-20 Lcw Les Colorants Wackherr Sa PIGMENTS BASED ON WATER-SOLUBLE DYES LINKED TO A MINERAL SUPPORT
FR2879097B1 (en) 2004-12-15 2007-04-13 Lcw Les Colorants Wackherr Sa PIGMENTS BASED ON WATER-SOLUBLE COLORANTS
EP1928404A2 (en) 2005-08-09 2008-06-11 Soane Labs, LLC Hair hold formulations
WO2007021731A2 (en) 2005-08-09 2007-02-22 Soane Laboratories, Llc. Dye-attached and/or surface-modified pigments
CA2641309A1 (en) 2006-02-03 2007-08-16 Nanopaper Llc Functionalization of paper components with an amine-containing polymer
CA2666139A1 (en) 2006-10-27 2008-05-15 Nanopaper, Llc Pigments for colored paper

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5061346A (en) * 1988-09-02 1991-10-29 Betz Paperchem, Inc. Papermaking using cationic starch and carboxymethyl cellulose or its additionally substituted derivatives
US5200036A (en) * 1990-04-30 1993-04-06 The Procter & Gamble Company Paper with polycationic latex strength agent
USRE35151E (en) * 1991-02-20 1996-01-30 Fuji Spinning Company, Limited Modified cellulose regenerated fiber comprising chitosan particles
US5807636A (en) * 1994-12-16 1998-09-15 Advanced Surface Technology Durable hydrophilic surface coatings
US5827610A (en) * 1997-01-10 1998-10-27 E. I. Du Pont De Nemours And Company Chitosan-coated pulp, a paper using the pulp, and a process for making them
US20020088579A1 (en) * 1998-11-23 2002-07-11 Sven Forsberg Method of producing a particle or group of particles having a coating of polymers interacting with each other
US6767553B2 (en) * 2001-12-18 2004-07-27 Kimberly-Clark Worldwide, Inc. Natural fibers treated with acidic odor control/binder systems
US20030134120A1 (en) * 2001-12-24 2003-07-17 Ibeks Technologies Co., Ltd. Natural fiber coated with chitosan and a method for producing the same
US6939443B2 (en) * 2002-06-19 2005-09-06 Lanxess Corporation Anionic functional promoter and charge control agent
US6936136B2 (en) * 2002-12-31 2005-08-30 Kimberly-Clark Worldwide, Inc. Amino-functionalized pulp fibers

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Definition of Pulp, "Paper Glossary & Dictionary", Paper Machinery, 2006, [online], 2 pages, Retrieved from the Internet [retrieved 01/30/2014], . *
Smook, Gary A., Handbook for Pulp and Paper Technologists, 2nd ed, Angus Wilde Publications, 1992, pp 283-289. *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120152476A1 (en) * 2009-08-12 2012-06-21 Nanopaper, Llc High strength paper
US8980059B2 (en) * 2009-08-12 2015-03-17 Nanopaper, Llc High strength paper
US9587353B2 (en) 2012-06-15 2017-03-07 Nanopaper, Llc Additives for papermaking
US20240052571A1 (en) * 2022-08-03 2024-02-15 World Centric Moisture/oil resistant composite materials

Also Published As

Publication number Publication date
CA2641309A1 (en) 2007-08-16
WO2007092450A2 (en) 2007-08-16
WO2007092450A3 (en) 2007-11-22
EP1984564A4 (en) 2013-04-03
EP1984564A2 (en) 2008-10-29
US20090165975A1 (en) 2009-07-02
US8123906B2 (en) 2012-02-28

Similar Documents

Publication Publication Date Title
US8123906B2 (en) Functionalization of paper components
JP6050122B2 (en) Method for enhancing dry strength of paper by treatment with vinylamine-containing polymer and acrylamide-containing polymer
AU619599B2 (en) Dry strength additive for paper
CA2817004C (en) Composition and process for increasing the dry strength of a paper product
EP2556191B1 (en) Stable and aqueous compositions of polyvinylamines with catlonic starch, and utility for papermaking
AU2010208154B2 (en) Quaternary vinylamine-containing polymers as additives in papermaking
CN104884706B (en) By increasing the method for paper intensity using natural gum and dry strength reagent in wet end
WO2001086067A1 (en) Method for pretreatment of filler, modified filler with a hydrophobic polymer and use of the hydrophobic polymer
US20080271865A1 (en) Pigments for colored paper
EP2917406A1 (en) Method for treating a fibre stock for making of paper, board or the like and product
US20090165976A1 (en) Expansion agents for paper-based materials
US20170233947A1 (en) Additives for papermaking
AU663141B2 (en) Novel cationic compounds useful as drainage aids and stabilizers for rosin-based sizing agents
BRPI0917678B1 (en) process for the production of paper, cardboard and cardboard
CN111433407A (en) Paper strength improving polymer composition and additive system, use thereof and manufacture of paper products
US20080093040A1 (en) Papermaking Additive
US11453979B2 (en) Paper strength improving composition, manufacture thereof and use in paper making
CN106368060B (en) Ternary microparticle retention and drainage aid system
Sang et al. The adsorption of cationic PVA on cellulose fibres and its effect with polyelectrolyte complex on paper strength
CN109715884A (en) Paper product and the method for increasing its intensity
MICROGELS CHUANWEI MIAO, B. Eng, M. Sci.

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION