BACKGROUND OF THE INVENTION1. Field of Endeavor[0003]
The present invention relates to fibers and fabrics and more particularly to fibers and fabrics with insulating, waterproofing, and flame-resistant properties.[0004]
2. State of Technology[0005]
U.S. Pat. No. 6,040,251 for garments of barrier webs by J. Michael Caldwell, patented Mar. 21, 2000, incorporated herein by reference, provides the following background information, “Barrier fabrics are generally characterized by being impervious to penetration by liquids. There is a class of barrier fabrics which, additionally, are vapor permeable to provide what is termed breathability. Barrier fabrics are especially useful in the medical career apparel garments. The barrier fabrics in the prior art can be generally classified as disposable and reuseable. Disposable fabrics are typically constructed from nonwovens made from light weight synthetic fibers or synthetic fibers blended with natural fibers. Performance of disposable nonwoven fabrics in terms of liquid repellency and flame retardancy are quite acceptable. Reusable fabrics are normally woven and may be constructed from cotton or cotton/polyester blends of a high thread count to provide a physical barrier to prevent or reduce the spread of infectious materials and vectors.[0006]
While reusable woven fabrics generally offer more comfort in terms of drapeability, breathability, transmission of heat and water vapor, stiffness, etc., and improved (reduced) cost per use, they lack the liquid repellency the market has come to expect on the basis of experience with the disposables, especially after repeated launderings and/or steam (autoclave) sterilizations.[0007]
Woven reusable surgical barrier fabrics must meet or exceed the current criteria for National Fire Protection Association (NFPA-99) and the Association of Operating Room Nurses (AORN) “Recommended Practices-Aseptic Barrier Material for Surgical Gowns and Drapes” used in constructing operating room wearing apparel, draping and gowning materials. To be effective, the fabric must be resistant to blood and aqueous fluid (resist liquid penetration); abrasion resistant to withstand continued reprocessing; lint free to reduce the number of particles and to reduce the dissemination of particles into the wound; drapeable; sufficiently porous to eliminate heat buildup; and flame resistant.[0008]
Reusable fabrics should withstand multiple laundering and, where necessary, sterilization (autoclaving) cycles; be non-abrasive and free of toxic ingredients and non-fast dyes; be resistant to tears and punctures; provide an effective barrier to microbes, preferably be bacteriostatic in their own right; and the reusable material should maintain its integrity over its expected useful life.[0009]
None of the fabrics or the fabrics taught in the prior art has the physical characteristics of (1) being substantially resistant or impermeable to liquids, such as water, (2) being permeable to gases, and (3) impermeable to microorganisms. In addition, none of the fabrics taught in the prior art teach or suggest fabrics that are capable of selectively removing or retaining microorganisms or other particles or molecules from the surrounding milieu.[0010]
In the prior art, it has been proposed to treat porous webs, especially fabrics, with silicone resins and also with fluorochemicals. Conventional treatments of webs fall into the general categories of (i) surface coatings and (ii) saturations or impregnations.[0011]
For example, U.S. Pat. Nos. 3,436,366; 3,639,155; 4,472,470; 4,500,584; and 4,666,765 disclose silicone coated fabrics. Silicone coatings are known to exhibit relative inertness to extreme temperatures of both heat and cold and to be relatively resistant to ozone and ultraviolet light. Also, a silicone coating can selectively exhibit strength enhancement, flame retardancy and/or resistance to soiling. Fluorochemical treatment of webs is known to impart properties, such as soil resistance, grease resistance, and the like.[0012]
Prior art fluorochemical and silicone fabric treatment evidently can protect only that side of the fabric upon which they are disposed. Such treatments significantly alter the hand, or tactile feel, of the treated side. Prior silicone fabric coatings typically degrade the tactile finish, or hand, of the fabric and give the coated fabric side a rubberized finish which is not appealing for many fabric uses, particularly garments.[0013]
U.S. Pat. No. 4,454,191 describes a waterproof and moisture-conducting fabric coated with a hydrophilic polymer. The polymer is a compressed foam of an acrylic resin modified with polyvinyl chloride or polyurethane and serves as a sort of “sponge,” soaking up excess moisture vapor. Other microporous polymeric coatings have been used in prior art attempts to make a garment breathable, yet waterproof.[0014]
Various polyorganosiloxane compositions are taught in the prior art that can be used for making coatings that impart water-repellency to fabrics. Typical of such teachings is the process described in U.S. Pat. No. 4,370,365 which describes a water repellent agent comprising, in addition to an organohydrogenpolysiloxane, either one or a combination of linear organopolysiloxanes containing alkene groups, and a resinous organopolysiloxane containing tetrafunctional and monofunctional siloxane units. The resultant mixture is catalyzed for curing and dispersed into an aqueous emulsion. The fabric is dipped in the emulsion and heated. The resultant product is said to have a good “hand” and to possess waterproofness.[0015]
This type of treatment for rendering fabrics water repellent without affecting their “feel” is common and well known in the art. However, it has not been shown that polyorganosiloxanes have been coated on fabrics in such a way that both high levels of resistance to water by the fibers/filaments and high levels of permeability to water vapor are achieved. As used herein, the term “high levels of permeability to water vapor” has reference to a value of at least about 500 gms/m.sup.2/day, as measured by ASTM E96-80B. Also, as used herein, the term “high level of waterproofness” is defined by selective testing methodologies discussed later in this specification. These methodologies particularly deal with water resistance of fabrics and their component fibers.[0016]
Porous webs have been further shown to be surface coated in, for example, U.S. Pat. Nos. 4,478,895; 4,112,179; 4,297,265; 2,893,962; 4,504,549; 3,360,394; 4,293,611; 4,472,470; and 4,666,765. These surface coatings impart various characteristics to the surface of a web, but do not substantially impregnate the web fibers. Such coatings remain on the surface and do not provide a film over the individual internal fibers and/or yarn bundles of the web. In addition, such coatings on the web surface tend to wash away quickly.[0017]
Prior art treatments of webs by saturation or impregnation also suffer from limitations. Saturation, such as accomplished by padbath immersion, or the like, is capable of producing variable concentrations of a given saturant chemical.[0018]
To treat a flexible web, by heavy saturation or impregnation with a polymer material, such as a silicone resin, the prior art has suggested immersion of the flexible web, or fabric, in a padbath, or the like, using a low viscosity liquid silicone resin so that the low viscosity liquid can flow readily into, and be adsorbed or absorbed therewithin. The silicone resin treated product is typically a rubberized web, or fabric, that is very heavily impregnated with silicone. Such a treated web is substantially devoid of its original tactile and visual properties, and instead has the characteristic rubbery properties of a cured silicone polymer.[0019]
International Patent Application W00106054 A1 for nanoparticle-based permanent treatment for textiles by Soane et al, published Jan. 25, 2001 provides the following information, “an agent or other payload entrapped, that is, surrounded by or contained within a synthetic, polymer shell or matrix that is reactive to fibers, yarns, fabrics, or webs, to give textile-reactive beads or matrices. The beads or matrices are micrometric or nanometric in size, and are herein collectively and interchangeably referred to as “nanobeads” and “nanoparticles.” The nanobead/nanoparticle of the invention may comprise a polymeric shell surrounding the payload or it may comprise a three-dimensional polymeric network entrapping the payload, both of which are referred to herein as a polymer shell.” By “textile-reactive” is meant that the payload bead will form a chemical covalent bond with the fiber, yarn, fabric, textile, finished goods (including apparel), or other web or substrate to be treated. The polymer shell or polymer network of the payload nanoparticle has a surface that includes functional groups for binding or attachment to the fibers, filaments or structural components or elements (referred to collectively herein and in the appended claims as “fibers”) of the textiles or other webs to be treated, to provide permanent attachment of the payload to the fibers. Alternatively, the surface of the nanobead includes functional groups that can bind to a linker molecule that will in turn bind or attach the bead to the fiber. In either case, these functional groups are referred to herein as “textile-reactive functional groups” or “fiber-reactive functional groups” or “substrate-reactive functional groups.” The terms “payload” and “payload agent” as used herein refer collectively to any material or agent that would be desirable for permanent attachment to or treatment of a textile or other web. Alternatively, the payload agent may be released from the cage of the payload nanobead in a controlled and prolonged fashion. The chemical linkage on the surface of the nanobead does not involve the molecules of the payload. The payload agents are physically entrapped within the nanoparticle, thus requiring no chemical modifications of the agents themselves. The resulting encapsulated payload preparations or nanoparticles have improved retention within and on the textile or web fiber structure without changing the inherent character of the payload agent. The architecture of the shell or matrix of the nanobead can be formulated and fine-tuned to exhibit controlled release of the entrapped payload, ranging from constant but prolonged release (desirable for drugs, biologic or anti-biologic agents, softeners, and fragrances, for example) to zero release (desirable for dyes, metallic reflector colloids, and sunblock agents, for example). In an encapsulated configuration, the beads will desirably insulate the payload from the skin, preventing potential allergic reactions. In addition, the nanoparticle can be designed to respond to different environmental stimuli (such as temperature, light change, pH, or moisture) to increase the rate of release, color change, or temperature change at certain times or in certain selected spots or locations on the textile or finished good. This invention is further directed to the fibers, yarns, fabrics (which may be woven, knitted, stitch-bonded or nonwoven), other textiles, or finished goods (encompassed collectively herein under the terms “textiles” or “webs”) treated with the textile-reactive nanoparticles. Such textiles and webs exhibit a greatly improved retention or durability of the payload agent and its activity, even after multiple washings. Methods are provided for synthesizing a textile-reactive payload-containing nanoparticle. The preparations of the invention may be formed via one of several methods of encapsulation, such as interfacial polymerization, microemulsion polymerization, precipitation polymerization, and diffusion. Multi-component mixture preparation followed by atom ization/spraying into a drying chamber is yet another processing scheme. Reactive functional groups on the polymer shell provide a means for attaching the payload nanoparticles to textiles.”[0020]
U.S. Pat. No. 2,673,823 teaches impregnating a polymer into the interstices of a fabric and thus fully filling the interstices. This patent provides no control of the saturation of the fabric. It teaches full saturation of the interstices of the fabric.[0021]
The prior art application of liquid or paste compositions to textiles for purposes of saturation and/or impregnation is typically accomplished by an immersion process. Particularly for flexible webs, including fabric, an immersion application of a liquid or paste composition to the web is achieved, for example, by the so-called padding process wherein a fabric material is passed first through a bath and subsequently through squeeze rollers in the process sometimes called single-dip, single-nip padding. Alternatively, for example, the fabric can be passed between squeeze rollers, the bottom one of which carries the liquid or paste composition in a process sometimes called double-dip or double-nip padding.[0022]
Prior art treatment of webs that force a composition into the spaces of the web while maintaining some breathability have relied on using low viscosity compositions or solvents to aid in the flow of the composition. U.S. Pat. No. 3,594,213 describes a process for impregnating or coating fabrics with liquefied compositions to create a breathable fabric. This patent imparts no energy into the composition to liquefy it while forcing it into the spaces of the web. The composition is substantially liquefied before placement onto and into the web. U.S. Pat. No. 4,588,614 teaches a method for incorporating an active agent into a porous substrate.[0023]
This patent utilizes a solvent to aid in the incorporation of the active agent into the web. Prior art apparatus for the coating of webs, including fabrics, generally deposits a coating onto the fabric at a desired thickness. Coating at a predetermined thickness can be achieved by deposition of coating material or by the scraping of a coating upon the fabric by knives. Flexible webs are generally urged between oppositely disposed surfaces, one of which would be a doctoring blade or drag knife. The blade or knife smooth the coating and maintain the thickness of the coating to a desired thickness. For example, it is possible to apply a relatively thick silicone liquid elastomer coating to a rough web, typically of fiberglass, in order to make architectural fabric as is taught in U.S. Pat. No. 4,666,765. In this example, the drag knives are set to a thickness of about 2 to 10 mils thicker than the web thickness. This setting, depending on the coating speed, can yield a base coat thickness of approximately 3 to 12 mils thicker than the web thickness.[0024]
Various types of coatings, and various coating thicknesses, are possible. However, a general principle of coating machinery is that the coating material is swept, or dragged, along the surface of the fabric. No special attention is normally given to any pressured forcing of the coating into the fabric, therein making the coating also serve as an impregnant. Of course, some coating will be urged into surface regions of the fabric by the coating process. Generally, however, application of high transversely exerted (against a fiber or web surface) forces at the location of the coating deposition and/or smoothing is not desired in the prior art processes because it is the goal of the prior art coating processes to leave a definite thickness of coating material upon a surface of the fabric, and not to scrape the fabric clean of surface-located coating material.[0025]
One prior art silicone resin composition is taught by U.S. Pat. Nos. 4,472,470 and 4,500,584, and includes a vinyl terminated polysiloxane, typically one having a viscosity of up to about 2,000,000 centipoises at 25.degree. C., and a resinous organosiloxane polymer. The composition further includes a platinum catalyst, and an organohydrogenpolysiloxane crosslinking agent, and is typically liquid. Such composition is curable at temperatures ranging from room temperature to 100 C or higher depending upon such variables as the amount of platinum catalyst present in the composition, and the time and the temperature allowed for curing.[0026]
Such compositions may additionally include fillers, including finely divided inorganic fillers. Silicone resin compositions that are free of any fillers are generally transparent or translucent, whereas silicone resin compositions containing fillers are translucent or opaque depending upon the particular filler employed. Cured silicone resin compositions are variously more resinous, or hard, dependent upon such variables as the ratio of resinous copolymer to vinyl terminated polysiloxane, the viscosity of the polysiloxane, and the like.[0027]
Curing (including polymerization and controlled crosslinking) can encompass the same reactions. However, in the fabric finishing arts, such terms can be used to identify different phenomena. Thus, controllable and controlled curing, which is taught by the prior art, may not be the same as control of crosslinking. In the fabric finishing arts, curing is a process by which resins or plastics are set in or on textile materials, usually by heating. Controlled crosslinking may be considered to be a separate chemical reaction from curing in the fabric finishing arts. Controlled crosslinking can occur between substances that are already cured. Controlled crosslinking can stabilize fibers, such as cellulosic fibers through chemical reaction with certain compounds applied thereto. Controlled crosslinking can improve mechanical factors such as wrinkle performance and can significantly improve and control the hand and drape of the web. Polymerization can refer to polymer formation or polymer growth.[0028]
What is needed in the industry is a barrier fabric that is impermeable to liquids, is permeable to gases, and is impermeable to microorganisms. In addition, what is needed are methods and processes for producing fabrics with predetermined pore sizes that allow the manufacturer to produce a fabric with a desired pore size.”[0029]
European Patent No. EP0846802 for a method of filling a hollow fiber with gel by Hajime Izawa and Togi Suzuki of Teijin Limited-Osaka Research Center, published Jun. 10, 1998, incorporated herein by reference, provides the following description, “This invention provides a method for filling a hollow portion of a hollow fiber with a gel without requiring special equipment such as pressure resistant facilities and enabling an industrial mass production, which comprises immersing said hollow fiber on the surface of which pores are diffusely distributed to communicate to said hollow portion in a gelable liquid, leaving said hollow fiber at room temperature so that said gelable liquid may be absorbed through said pores into the hollow portion, and finally causing thus absorbed gelable liquid gelled.”[0030]
U.S. Pat. No. 5,830,548 for articles of manufacture and methods for manufacturing laminate structures including inorganically filled sheets by Per Just Andersen and Simon K. Hodson, patented Nov. 3, 1998, incorporated herein by reference, provides the following description, “Compositions and methods for manufacturing composite laminate structures incorporating sheets having a moldable matrix are disclosed. Suitable compositions are prepared by mixing together a water dispersable organic binder, water, and appropriate additives (such as aggregates and fibers) which impart predetermined properties so that a sheet formed therefrom has the desired performance criteria. The compositions are formed into sheets by first extruding them into a sheet and then calendaring the sheet using a set of rollers. The calendered sheets are dried in an accelerated manner to form a substantially hardened sheet. The drying process is performed by heated rollers and/or a drying chamber. The inorganically filled sheets so formed may have properties substantially similar to sheets made from presently used materials like paper, cardboard, polystyrene, or plastic. Such sheets can be rolled, pressed, scored, perforated, folded, and glued before or after being incorporated into composite laminate structures. Such composite laminate structures have especial utility in the mass production of containers, particularly food and beverage containers.”[0031]
U.S. Pat. No. 6,129,978 for Porous webs having a polymer composition controllably placed therein by J. Michael Caldwell, patented Oct. 10, 2000, incorporated herein by reference, provides the following description, “The present invention relates to a porous web comprising a plurality of structural elements with interstitial spaces therebetween, wherein at least some of the structural elements of the top and bottom surfaces of the web are encapsulated by a cured, shear thinned polymer composition and most of the interstitial spaces are open. The invention also relates to a porous web having a substantially continuous region of a cured, shear thinned polymer composition extending through the web so that the polymer composition fills the interstitial spaces and adheres adjacent structural elements of the web in the region. In the areas of the web above and below the filled region, at least some of the structural elements are encapsulated and most of the interstitial spaces are open.”[0032]
U.S. Pat. No. 6,180,037 for methods for the manufacture of sheets having a highly inorganically filled organic polymer matrix by Just Andersen and Simon K. Hodson, patented Jan. 30, 2001, provides the following description, “Compositions and methods for manufacturing sheets having a highly inorganically filled matrix. Suitable inorganically filled mixtures are prepared by mixing together an organic polymer binder, water, one or more inorganic aggregate materials, fibers, and optional admixtures in the correct proportions in order to form a sheet which has the desired performance criteria. The inorganically filled mixtures are formed into sheets by first extruding the mixtures and the passing the extruded materials between a set of rollers. The rolled sheets are dried in an accelerated manner to form a substantially hardened sheet, such as by heated rollers and/or a drying chamber. The inorganically filled sheets may have properties substantially similar to sheets presently made from traditional materials like paper, cardboard, polystyrene, plastic, or metal. Such sheets can be rolled, pressed, scored, perforated, folded, and glued. They have especial utility in the mass production of containers, particularly food and beverage containers.”[0033]
SUMMARY OF THE INVENTIONFeatures and advantages of the present invention will become apparent from the following description. Applicants are providing this description, which includes drawings and examples of specific embodiments, to give a broad representation of the invention. Various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this description and by practice of the invention. The scope of the invention is not intended to be limited to the particular forms disclosed and the invention covers all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the claims.[0034]
The present invention provides fibers and fabrics that have desirable properties. Embodiments of the invention provide fibers and fabrics that have insulating, waterproofing, and/or fire resistant properties. In various embodiment of the invention, fibers, and fabrics produced from the fibers, are made water repellent, fire-retardant and/or thermally insulating by filling the void spaces in the fibers and/or fabrics with a powdered material. When the powder is sufficiently finely divided, it clings tenaciously to the fabric's fibers and to itself, resisting the tendency to be removed from the fabric. The present invention has many uses including uses for military clothing, blankets, tents, raingear, fire/flame protection clothing, blankets, tents, raingear, fire/flame protection, etc.[0035]
In one embodiment of the invention a single fiber strand includes a porous fiber strand having voids. At least some of the voids are at least partially filled with particles in the size range of 1-500 nm. In another embodiment a single fiber is made up of multiplicity of smaller single fiber strands. The smaller single porous fiber strands have voids and at least some of the voids are at least partially filled with particles in the size range of 1-500 nm. In another embodiment of the invention a single fiber is made up of multiplicity of smaller single fiber strands. The multiplicity of smaller single porous or non-porous fiber strands have voids between the smaller single porous or non-porous fiber strands. At least a portion of the voids are at least partially filled with particles in the size range of 1-500 nm.[0036]
In various embodiments of the invention the particles are at least partially composed of at least one of the following: a porous material, or a nanoporous material, or a nanoporous powdered material, or a solgel derived material, or an aerogel-like material, or an aerogel, or an inorganic material, or aggregates of inorganic particle material, or combinations of the materials. In other embodiments of the invention the particles are at least partially composed of at least one of the following: an insulating material, or a thermally insulating material, or a water repellant material, or a hydrophobic material, or a hydrophobic, nanoporous powdered material, or a hydrophobic silica aerogel, or a fire resistant material, or combinations of the materials. The present invention is not be limited to silica aerogels, other metal oxide aerogels, e.g., alumina, zirconia, tantala, titania, etc., and carbon aerogels are included. The present invention also includes laminates of aerogel powder or powder impregnated fabrics, with other fabrics—where the aerogel layer provides the physical properties of repellancy, fire resistence, and thermal resistence (as well as providing other barrier possibilities by absorption.)[0037]
Another embodiment of the present invention provides a method of producing a fiber. A porous fiber strand containing voids is provided. The voids are filled with particles in the size range of 1-500 nm. The particles are at least partially composed of at least one of the following: a porous material, or a nanoporous material, or a nanoporous powdered material, or a solgel derived material, or an aerogel-like material, or an aerogel, or an inorganic material, or aggregates of inorganic particle material, or an insulating material, or a thermally insulating material, or a water repellant material, or a hydrophobic material, or a hydrophobic, nanoporous powdered material, or a hydrophobic silica aerogel, or a fire resistant material, or combinations of the materials. The present invention is not be limited to silica aerogels, other metal oxide aerogels, e.g., alumina, zirconia, tantala, titania, etc., and carbon aerogels are included. The method includes the step of: filling the voids with a solution which precipitates particles as it dries, or filling the voids with a solution containing a colloidal suspension of particles which remain when the liquid dries, or filling the voids with a dry powder by passing the fibers through the powder in a manner in which the particles attach to the fibers, or filling the voids with a dry powder by passing the powder over the fibers in a manner in which the particles attach to the fibers, or filling the voids with a dry powder by forcing dry powder to enter the space using rollers, or filling the voids with a dry powder by forcing dry powder to enter the space using a press, or combinations of the steps.[0038]
Another embodiment of the present invention provides a method of producing a fiber made up of multiplicity of smaller single fiber strands. Voids are located between the smaller single fiber strands. The voids are filled with particles in the size range of 1-500 nm. In various embodiments the particles are at least partially composed of at least one of the following: a porous material, or a nanoporous material, or a nanoporous powdered material, or a solgel derived material, or an aerogel-like material, or an aerogel, or an inorganic material, or aggregates of inorganic particle material, or an insulating material, or a thermally insulating material, or a water repellant material, or a hydrophobic material, or a hydrophobic, nanoporous powdered material, or a hydrophobic silica aerogel, or a fire resistant material, or combinations of the materials. The present invention is not be limited to silica aerogels, other metal oxide aerogels, e.g., alumina, zirconia, tantala, titania, etc., and carbon aerogels are included. The method includes the step of: filling the voids with a solution which precipitates particles as it dries, or filling the voids with a solution containing a colloidal suspension of particles which remain when the liquid dries, or filling the voids with a dry powder by passing the fibers through the powder in a manner in which the particles attach to the fibers, or filling the voids with a dry powder by passing the powder over the fibers in a manner in which the particles attach to the fibers, or filling the voids with a dry powder by forcing dry powder to enter the space using rollers, or filling the voids with a dry powder by forcing dry powder to enter the space using a press, or combinations of the steps.[0039]
Another embodiment of the invention provides a method of producing a fabric. A multiplicity of fibers is located in association with each other to form the fabric. The fibers containing a void volume located either in the fibers or between the fibers or both in the fibers and between the fibers. At least a portion of the void volume is filled with particles in the size range of 1-500 nm. In various embodiments the particles are at least partially composed of at least one of the following: a porous material, or a nanoporous material, or a nanoporous powdered material, or a solgel derived material, or an aerogel-like material, or an aerogel, or an inorganic material, or aggregates of inorganic particle material, or an insulating material, or a thermally insulating material, or a water repellant material, or a hydrophobic material, or a hydrophobic, nanoporous powdered material, or a hydrophobic silica aerogel, or a fire resistant material, or combinations of the materials. The present invention is not be limited to silica aerogels, other metal oxide aerogels, e.g., alumina, zirconia, tantala, titania, etc., and carbon aerogels are included. The method includes the step of: filling the voids with a solution which precipitates particles as it dries, or filling the voids with a solution containing a colloidal suspension of particles which remain when the liquid dries, or filling the voids with a dry powder by passing the fibers through the powder in a manner in which the particles attach to the fibers, or filling the voids with a dry powder by passing the powder over the fibers in a manner in which the particles attach to the fibers, or filling the voids with a dry powder by forcing dry powder to enter the space using rollers, or filling the voids with a dry powder by forcing dry powder to enter the space using a press, or combinations of the steps.[0040]
The invention is susceptible to modifications and alternative forms. Specific embodiments are shown by way of example. It is to be understood that the invention is not limited to the particular forms disclosed. The invention covers all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the claims.[0041]