Indian Patents. 254178:"A SPUN FIBER HAVING AT LEAST TWO DEFFERENT MELTING POINTS"

Title of Invention	"A SPUN FIBER HAVING AT LEAST TWO DEFFERENT MELTING POINTS"
Abstract	A spun fiber having at least two different melting points, which comprises a composition itself comprising: a first fiber constituent having a first melting point; a second fiber constituent having a second melting point; and a gelling agent that solvates at least one of the first fiber constituent or the second fiber constituent.

Full Text	MULTIPHASE FIBER MATERIALS AJVD COMPOSITIONS, METHODS OF MANUFACTURE AND USES THEREOF LD OF THE SUBJECT MATTER The field of the subject matter herein is multiphase pre-fiber and fiber materials and compositions, fiber products, yarn products and carpet products, methods of manufacture and uses thereof. BACKGROUND i Fibers for consumer use, especially fibers that are incorporated into yams, carpet products and fabrics/textiles, are constantly being evaluated for improvements with respect to aesthetics and performance. These improvements may relate to appearance retention, texture and surface appearance, softness and floorweai performance. Fibers and fiber products are also being evaluated to determine if mere are more efficient and cost-effective manufacturing processes and equipment. Fibers, •which can be used in the production of carpet products, such as wall-to-wall carpet, rugs and mats, are modified and in some instances improved to provide a certain yarn texture when they are incorporated into a carpet product and to provide a desired "look" for the space where the carpet product is being used. Additional issues that arise in the design of carpet fiber material and carpet products are daily and long-term performance and appearance. One method that is being used to modify the texture of fabrics is to incorporate fibers mat have mixed deniers into the fabric product. Denier (or fibei denier) is a physical property of a particular fiber and can be defined as: "A direct yarn numbering measurement, it is die weight in grams of 9,000 meters of yarn. Therefore, the higher the denier, the larger the yarn. Typical nylon carpet fiber has 15-18 denier/filament." (see www.fabrica.com: Glossary of Fabric and Rug Terms) Another method that is being used to modify fibers and the resulting carpet or textile product is to incorporate not only fibers with mixed deniers, but also mixed lusters, such as the fiber and carpet product seen in commonly-owned US Patent Application Serial No.: 10/602459, which is incorporated herein by reference in its entirety. Another method of improving the aesthetics of carpet products that is related to the mixed denier method is to incorporate two fiber types - such as a low melt continuous (minority} fiber and a bulked continuous filament (BCF) host fiber. In order to create softer resultant carpets with improved tips, surface and texture, however, the concentration of the minority fiber needs to be reduced. The reduction in concentration of the low melt continuous minority fiber can be difficult because the concentration is ultimately limited by the denier of the minority fiber. In a conventional low melt/host fiber product, the low melt continuous fiber has a yarn denier of about 20-40 denier, and depending on the denier of the host fiber, the low melt fiber constituent can greatly influence the final properties of the resultant fiber and/or resultant carpet product. Traditionally, carpet yarn deniers range between 1000 and 1500. Caprolactam and nylon compounds have each been individually polymerized with the same compounds (i.e. caprolactam/caprolactam or nylon/nylon) by anionic polymerization in a twin-screw extruder and then tested for residual monomer content and thermal/mechanical properties: however, in both processes, there were no mixed monomer anionic polymerization, the polymerization process did not result in a pre-fiber gel composition that could be processed by any means (including extrusion), there was no pre-fiber dispersion, and there is no indication that the mechanical strength or thermal strength was improved by the single monomer/twin-screw extruder mixing process, (see Antec '93 Conference Proceedings, New Orleans, 9th- 13th May 1993, Vol. 1, p. 470-473; and Antec '94 Conference Proceedings, San Francisco, CA, lsl-5* May 1994, Vol. 1, p. 116-22) Therefore, it would be desirable to produce a multiphase pre-fiber and/or fiber material and/or composition that a) has sufficient viscosity and suitable melt strength such that it can be spun into a fiber or yam, b) can be processed by any processing method, including extrusion, c) can be incorporated into the production of a fiber, yarn, textile and/or carpet product, d) allows for reduction of the .concentration of or the effect of the low melt material component without being constrained by a particular fiber denier, e) would comprise at least two dispersed constituents and exhibits at least two definitive and differentiatable melting points, and f) would produce a composition, fiber and/or product having tv/o melting points whereby the melt temperature of the constituent having the lower melting point is maintained primarily by minimizing/preventing co-polymerization during i blending and processing steps, i SUMMARY OF THE SUBJECT MATTER A pre-fiber composition is disclosed herein that comprises: a) a first fiber constituent having a first melting point; b) a second fiber constituent having a second melting point; and c) a gelling agent that solvates at least one of the first fiber constituent or the second fiber constituent, wherein the gelling agent significantly reduces co-polymerization of either of the constituents in the composition. A fiber is also disclosed herein'that comprises: a) at least two amide-based polymers, each having a melting point, wherein the melting point of one amide-based polymer is dissimilar to the melting point of a second amide-based polymer; and b) a gelling agent that is compatible with at least one of the amide-based polymers, wherein the fiber comprises two differentiatable melting points that are substantially similar to the melting points of each of the amide-based polymers. A method of producing a pre-fiber composition is disclosed herein that comprises: a) providing a first fiber constituent having a first melting point; b) providing a second fiber constituent having a second melting point, wherein the first melting point and the second melting point are dissimilar; c) providing at least one gelling agent; and d) mixing the first constituent, the second constituent and the at least one gelling agent such that there is sufficient viscosity and sufficient melt strength in the composition so that it can be spun into a fiber and mch that the fust melting point and the second melting point in the fiber are substantially similar to their original values before mixing. BRIEF DESCRIPTION OF THE FIGURES Figure 1 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration. Figure 2 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration, Figure 3 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration. Figure 4 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration. Figure 5 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration. t Figure 6 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration. ' Figure 7 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration, Figure 8 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration. Figure 9 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration. Figure 10 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration. Figure 11 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration. Figure 12 shows data collected that relates to the onset of melting of the Dinder pha.se and the lactam concentration. Figure 13 shows data collected that relates to the onset of melting of the jinder phase and the lactam concentration. Figure 14 shows data collected that relates to the onset of melting of the . binder phase and the iactarn concentration. Figure 15 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration. Figure 16 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration. Figure 17 shows data collected that relates to fiber tenacity. i Figure 18 shows data collected that relates to fiber tenacity. Figure 19 shows data collected that relates to fiber tenacity. Figure 20 shows XRD data collected for a contemplated embodiment of the subject matter herein. Figure. 21 shows data collected that relates to the %UE of a contemplated embodiment of the subject matter herein. Figure 22 shows data collected that relates to the %UE of a contemplated embodiment of the subject matter herein. Figure 23 shows data collected that relates to the %UE of a contemplated embodiment of the subject matter herein. i Figure 24 shows data collected that relates to the melting point versus the Tecliriic concentration in a contemplated embodiment of the subject matter herein. Figure 25 shows XRD data collected for a contemplated embodiment of the subject matter herein. Figure 26 shows XRD data collected for a contemplated embodiment of the subject matter herein. Figure 27 shows XRD data collected for a contemplated embodiment of the subject matter herein. DETAILED DESCRIPTION A multiphase pre-fiber and/or fiber material and/or composition has been produced that a) has sufficient viscosity and suitable melt strength such that it can be spun into a fiber or yarn, b) can be processed by any processing method,, including extrusion, c) can be incorporated into the production of a fiber, yarn, textile and/or carpet product, d) allows for reduction of the concentration of or the effect of the low melt material component without being constrained by a .particular fiber denier, e) comprises at least two dispersed constituents and exhibits at least two definitive and differentiatable melting points, and f) can produce a composition, fiber and/or product having at least two constituents each with a different melting point whereby the melt temperature of the constituent having the lower melting point is maintained primarily by minimizing/preventing co-polymerization during blending and processing steps. These pre-fiber and fiber materials and/or compositions at temperatures are also able to be processed at or below normal processing temperatures for a nylon fiber product. Tn some embodiments, there is a formation of a multiphase pre-fiber and/or fiber gel-spun composition and/or material that allows for the control of the properties of the drawn liber by allowing for more favorable orientation of the polymer molecules in the fiber. Controlling the molecule orientation can lead to increased tensile strength and an overall fiber improvement in the fiber physical properties. Furthermore, at least part of the at least one gelling agent can be removed and recovered from the spun fiber once formed. Formation of one of the embodiments - the pre-fiber gel composition - is also described in commonly-owned US Utility Application entitled "Pre-fiber Gel Materials and Compositions, Methods of Manufacture and Uses Thereof (Serial No. not yet assigned) that has been filed concurrently and is incoiporated herein in its entirety by reference. In order to produce a pre-fiber composition, dispersion and/or material that can be formed into a gel spun fiber, a contemplated pre-fiber composition includes, a) a first fiber constituent having a first melting point: b) a second fiber constituent having a second melting point; and c) a gelling agent that solvates at least one of the first fiber constituent or the 'second fiber constituent while at the same time minimizing and/or preventing co-polymerization of the first constituent with the second constituent or either of the individual components with itself (for example, first constituent-first constituent intermolecular or intramolecular polymerization). In other embodiments, the addition of the at least one gelling agent forms a gel composition that has sufficient viscosity and sufficient melt strength upon the mixing of the first fiber constituent, the second fiber constituent i and the at least one gelling agent that the composition can be spun into a fiber. i At this point it should be understood that, unless otherwise indicated, all numbers expressing quantities of ingredients, constituents, interaction conditions and so forth used in the specification and claims are to be understood as being* modified in all instances by the term "about". Accordingly, unless indicated to the contrary, the numerical parameters set forth in the specification and attached claims are approximations that may vary depending upon the desired properties sought to be obtained by the subject matter presented herein. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the subject matter presented herein are approximations., the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contain certain errors ' necessarily resulting from the standard deviation found in then- respective testing measurements. A first fiber constituent and a second fiber constituent are the starting points for the formation of a pre-fiber composition, dispersion and/or material, and the mixture of the two can be characterized as a "binder alloy fiber" or an "alloy mixture". It should be understood that the first fiber constituent and the second fiber constituent may comprise any suitable monomer, polymer or moiety, as long as each individual or both combined constituents is capable of being used as a fiber material, especially in yarn products, fabric/textile products and/or carpet products. In one embodiment, the first fiber constituent may comprise at least one amide-based compound and/or polyamide-based compound and the second liber constituent may comprise at least one second amide-based compound and/or polyamide-based compound. As used herein, the term "compound" means a substance with constant composition that can be broken down into elements by chemical processes. Polyamides and polyamide-based compounds, as the name implies, are polymers that comprise amide monomers. Several contemplated polyamide-based compounds comprise nylon-6, nylon-6,6, "nylon-6,6,6" (uylon-6/nyIon-6,6 copolymer) and/or nylon-12. Amides are an important group of nitrogenous compounds and monomers that are used as intermediates and/or building blocks in the production of polymers, textiles, plastics and adhesives. Amide monomers are generally' represented by the following formula: O II RCNH wherein R is an alkyl group, an aryl group, a cyclic allcyl group, an alkenyl group, an arylalkylene group, or any other appropriate group that can be utilized to be a part of an amide compound. As used herein, the term "monomer" generally refers to any chemical compound that is capable of forming a covalent bond with itself or a chemically iifferent compound in a repetitive manner. The repetitive bond formation between aionomers may lead to a linear, branched, super-branched, or three-dimensional product. Furthermore, monomers may themselves comprise repetitive building blocks, and when polymerized the polymers formed from such monomers are then termed "blockpolymers'". The weight-average molecular weight of monomers may vary greatly between about 40 Dalton and 20000 Dalton. However, especially when monomers comprise repetitive building blocks., monomers may have even higher molecular weights. Monomers may also include additional groups, such as groups used for crosslinking, radiolabeling. and/or chemical or environmental protecting. The term "alkyl" is used herein to mean a branched or a straight-chain saturated hydrocarbon group or substituent of 1 to 24 carbon atoms, such as i methyl, ethyl, n-propyl. isopropyl, n-butyl, isobutyl, t-butyl, octyl, decyl, tetradecyl, hexadecyl. eicosyl, tetracosyl and the like. In some embodiments, contemplated alkyl groups contain 1 to 12 carbon atoms. The term "cyclic alkyl" means an alkyl compound whose structure is characterized by one or more closed rings. The cyclic alkyl may be mono-, bi-, tri- or polycyclic depending on the number of rings present in the compound. The term "aryl" is used herein to mean a monocyclic aromatic species of 5 to 7 carbon atoms or a compound that is buiit with monocyclic aromatic species of 5 to 7 carbon atoms and is typically phenyl, naphthalyl, phenanthryl, anthracyl etc. Optionally, these groups are substituted with one to four, more preferably one to two alkyl. alkoxy, hydroxy, and/or nitro substituents. i The term "alkenyl" is used herein to mean a branched or a straight-chain hydrocarbon chain containing from 2 to 24 carbon atoms and at least one double bond. Preferred alkenyl groups herein contain 1 to 12 carbon atoms. The term "alkoxy" is used herein to mean an alkyl group bound through a single, terminal ether linkage; that is, an alkoxy group may be defined as -OR wherein R is an alley) group, as defined above. The term "arylalkylene" is used herein to mean moieties containing both alkylene and monocyclic aryl species, typically containing less than about 12 carbon atoms in the alkylene portion, and wherein the aryl substituent is bonded to the structure of interest tlirough an alkylene [inking group. Exemplary arylalkylene groups have the structure -(CH2)j-Ar wherein "j" is an integer in the range of 1 to 6 and wherein "Ar" is an aryl species. . The first fiber constituent comprises a first melting point and the second fiber constituent has a second melting point, and it should be understood that the first melting point and the second melting point are different from one another. Melting points can be determined by any available method, including differential scanning calorimetry (DSC), which is used herein and shown in the Examples section. It should further be understood that these at least two melting points are found in the same pre-fiber composition and/or the same fiber before the fiber is formed and after the fiber is formed/spun. In additional embodiments, at least one additional fiber constituent may be added to the pre-fiber composition and/or dispersion, wherein the at least one additional fiber constituent has at least one additional melting point that is measurably different from both the first melting point and the second melting point. > At least one gelling agent is provided mat is mixed and/or blended with the first or second fiber constituent, the at least one poiyamide-based or the at least one amide-based compound in order to fonn a contemplated pre-fiber composition and/or dispersion. The at least one gelling agent may comprise any suitable solvent that a) can solvate and is compatible with either the first or the second fiber constituent and b) is at least partially compatible with the other fiber constituents) in the pre-fiber composition. As mentioned, a suitable gelling agent is one that is compatible with either the first or the second fiber constituent. The term "compatible" means mat gelling agent that does not contribute any negative effects to the pre-fiber composition, such as by making one of the constituents "watery", by reacting with either the first or second fiber constituent (or additional constituents), by making the dispersion "non-spinnable", by making the "low melt" constituent into a composition that does not retain its low melting point, by inducing co-polymerization in the dispersion between or among any of the constituents and combinations of any of these negative effects thereof. In some embodiments, especially those embodiments where the first fiber constituent and the second fiber constituent comprise amide-based compounds. the getting agent comprises a iactam. It should be understood that lactam is a . suitable gelling agent because, in the embodiments where the first fiber constituent and the second fiber constituent comprise amide-based compounds, lactam is very compatible with at least one of the first fiber constituent or the second fiber constituent and is at least partially compatible with the other fiber constiruent(s). In yet other embodiments, the lactam-based gelling agent comprises a caprolactam, such as e-caprolactam. s-Caprolactam, also known as aminocaproic lactam and 2-oxohexamethyleneirnme, is a compound that is produced in flake and molten forms and is used primarily in the manufacture of nylon-6 and nylon-6,6,6 products such as those products contemplated herein or other synthetic fibers, plastics, bristles, films, coatings, synthetic leathers, plasticizers and paint vehicles. Caprolactam can also be used as a cross-linking agent for polyurethanes and in the synthesis of the amino acid lysine. A contemplated lactam preparation method is shown herein in Example 1. Amides, such as caprolactam, can also be produced by reacting a ketone with hydroxylamine to make an oxime, and then using an acid catalyzed rearrangement of the oxime(s), conventionally called the Beckmann rearrangement, to form the amide. Merchant quality caprolactam can be produced i by methods described in US Patent Application Serial No.: 10/251335 filed on September 21, 2002, which is commonly owned and herein incorporated in its entirety. The at least one gelling agent may be added in any suitable weight percentage with respect to the other composition/dispersion constituents, as long as the addition of the gelling agent aids in the production of a pre-fiber composition/dispersion. In a contemplated embodiment, the at least one gelling agent comprises less than 50 weight percent of the composition/dispersion. In another contemplated embodiment, the at least one gelling agent comprises less than 40 weight percent of the composition/dispersion. In yet another contemplated embodiment, the at least one gelling agent comprises less than 30 weight percent of the composition/dispersion. In other contemplated embodiments, the at least one gelling agent comprises less than 20 weight percent of the composition/dispersion. In yet other contemplated embodiments, the at least one gelling agent comprises less than 10 weight percent of the composition/dispersion. Also, in some contemplated embodiments, the at least one gelling agent comprises less than 5 weight percent of the composition/dispersion. Once the pre-fiber composition/dispersion is formed, the composition/dispersion may be extruded through a suitable die or spinnerette for production of a "minority" fiber. It should be understood that the resulting fiber will comprise the first fiber constituent having and retaining a first melting point (at or near its original melting point) and the second fiber constituent having and retaining a second melting point (at or near its original melting point), whereby co-polymerization between any or all of the constituents has been minimized and/or prevented entirely through the addition of the gelling agent. The minority fiber may then be combined with a "host" fiber or bulked continuous filament (BCF) "host" fiber to create a carpet product mat is softer than conventional carpet products made with conventional low melt fiber comprising 100% low melt co-polymer and that comprises improved tips, surface and texture, as opposed to conventional carpet products made without the addition of low melt fibers. These conventional melt-blended polymer fibers generally comprise significant and undesirable co-polymerization, such that the melt point of the low melt polymer increases as the amount of the higher melt point polymer increases. These fibers will not melt and bond at the temperature of the original low melt polymer and hence not effect the aesthetics of the resultant carpets if heat treated at the same temperature. In addition, a method of producing a pre-fiber composition and/or dispersion includes: a) providing a first fiber constituent having a first melting point; b) providing a second fiber constituent having a second melting point, wherein the first melting point and the second melting point are dissimilar; c) providing at least one gelling agent: and d) mixing the first fiber constituent, the second liber coJisuiusru ana me at least one' gelling agent such that there is .sufficient viscosity and sufficient melt strength in the composition so that it can be spun into a fiber while at the same time minimizing and/or preventing co-polyinerization between any of the constituents. Once the pre-fiber composition and/or dispersion is formed, it can be formed into a fiber, which can in turn be combined with a host fiber to form a yarn and then a carpet product having improved tips, surface and texture. i The first fiber constituent, the second fiber constituent, the at least one gelling agent and/or the at least one additional constituent and/or gelling agent may be provided by any suitable method, including a) buying at least some of the first fiber constituent, the second fiber constituent, the at least one gelling agent and/or the at least one additional constituent and/or gelling agent from a supplier or textile mill; b) preparing or producing at least some of the first fiber constituent, the second fiber constituent, the at least one gelling agent and/or the at least one additional constituent and/or gelling agent in house using chemicals provided by another source and/or c) preparing or producing at least some of the first fiber constituent, the second fiber constituent, the at least one gelling agent and/or the at least one additional constituent and/or gelling agent in house using chemicals also produced or provided in house or at the location. ! During or after the formation of contemplated pre-fiber compositions, gel-spun fiber materials, yarn products and/or carpet products, a thermal energy may be applied to the materials and/or products, wherein the thermal energy comprises a temperature that is below, at or above the melting point of the higher melting point constituent, the fiber and/or other heat-active components. The thermal energy can be applied to activate at least some of the plurality of fibers. In some embodiments, activating the fibers comprises forming chemical, such as covalent, ionic or hydrogen and/or physical, such as adhesion, bonds between at least some of the plurality of fibers and at least one of the other components. It should be understood, however, that the thermal energy will not induce co-polymerization between any of the constituents in the minority fiber or pre-fiber composition. It should also be understood that regardless of the temperature of the thermal energy that is applied - whether its below, at or above the melting point of the higher melting fiber constituent - the pre-fiber composition and/or fiber product continues to maintain at least two distinct and differentiatable melting points. The thermal energy may come from any suitable source, including extended/non-point sources, such as a UV-VIS source, an infra-red source, a heat source, both radiative and convective. or a microwave source; or electron sources, such as electron guns or plasma sources. Other suitable energy sources include electron beams, and radiative devices at non-IR wavelengths including x-ray, and gamma ray. Still other suitable energy sources include vibrational sources such as microwave transmitters. In preferred embodiments, the energy source is an extended source. In more preferred embodiments, the energy source is a heat source, such as an atmospheric pressure forced air machine, which can be followed by a steam purge, or a pressurized twist-setting machine. An example of ail atmospheric pressure forced air machine is the Suessen® Twist-Setting , Machine. Examples of pressurized twist-setting machines are those of the autoclave-type and those manufactured by Superba®. It should be understood that the thermal energy may be applied consistently or in short bursts. It is also contemplated that the thermal energy may be gradually and continuously applied over a temperature range until the thermal energy is at or above the melting point of the fiber or other heat-active components. For example, the fiber material and/or yarn may be heated by an atmospheric pressure forced air machine at a temperature of about 195°C for a residence time of about 60 seconds, before the treated fiber material and/or yarn product is tufted. The thermal energy may also be immediately applied at or above the melting point of the binder fiber and/or other heat-active components without any ramp time. It should also be understood that the temperature at which the low melt polymer phase melts is generally dependent on the atmospheric conditions. For example, the melt point of polyamides are depressed in the presence of water. The pre-fiber materials contemplated and described herein may be used . alone or in combination with oilier materials and/or products to form any suitable product, including a spun fiber product, a yam product, a fabric product and/or a carpet product. EXAMPLES The pre-fiber composition, spun and gel-spun fiber materials, yam products, carpet products and methods used to product those materials and products, as described in the examples, are for illustrative purpose only and should not, in any way, limit the scope of this invention. EXAMPLE 1 - L ACT AM PREPARATION Four liters of caprolactam were melted in a convection oven overnight in a covered container. The lactam was poured into a 5L 3-necked distillation flask with a magnetic stir bar and an electric heating mantle (top and bottom mantles). The distillation column was vacuum jacketed by a 29/42 column and a 10 tray-section, a 5 tray section, a splitting distillation head and a condenser. The condenser was held at 50°C with a heated water circulator. The system had the pressure reduced from 7 mm Hg to 4 mm Hg. Heat was applied and the column was brought to reflux conditions and held for 30 minutes. After 30 minutes for the column to stabilize, the distillation head splitter was activated with a 4 second take off and a 10 second reflux. Slightly less than 1 liter-of lactam was distilled off. The heat was turned off and the mantles were removed allowing the lactam in the 5-liter flask to drop to 90UC before breaking the vacuum on the system. The 5-liter flask was removed and the lactam was poured into 1 -liter nalgene beakers and promptly placed into a glove box with a dry nitrogen atmosphere. After cooling overnight, the crystal lactam was transferred to plastic bags and was broken into flake form with a hammer inside the glove box. The lactam was stored inside the dry glove box under house nitrogen until needf-d for the pre-fiber gel composition formation. EXAMPLE: 2 - A CONTEMPLATED PRE-FIBER GEL COMPOSITION FORMATION Nylon-6 was ground to a fine powder and mixed with a lactam gelling agent, which was in this case - caprolactam. A Braybender rnixer was used to mix the nylon and caprolactam at a speed of 60 RPM. Addition time took about 5 minutes and the gd was allowed to mix for 15 minutes after charging at the temperature indicated. The samples were removed while the Braybender was running with a brass wipe stick. The samples were then ground in a Willey mill using a course screen. A weighted amount of each ground gel mix was extracted 16+ hours using a jacketed soxlet extractor. The extract was filtered using a folded #54 paper and rinsed into a 100 mL volumetric flask. The extract was brought to volume with deionized water and then analyzed by Gas Chromatography for % lactam using a Carbowax column.(Table Remove) The resulting gels were geJ spun orr an twin screw extruder. The gels spun into a fiber product surprisingly well and packages of liber were able to be prepared at most conventional spinning conditions. Furthermore, it was observed that extruder temperature could be dropped below conventional conditions for neat polymers, given that the gel compositions allowed for lower extruder pressures. Tables 1-5. shown below, give summaries of several of the spinning conditions utilized in these Examples. i EXAMPLE 3 - A CONTEMPLATED PRJE-FIBER COMPOSITION FORMATION i BACKGROUND: Conventional binder alloy samples (1-end of 22 denier/12 fils) were inserted into 1202 mp 2-ply yarns during cabling and Supeiba® heatset. Plybond tests of the yarns did not show any evidence of bonding after Superba® heatset. Subsequently, we autoclave heatset the yams followed by conversion into a banded carpet. No significant aesthetic effect in the carpet was observed with any of the conventional binder alloy samples. However, there was a slight impact (firmness) on carpet hand at the lowest nylon/binder ratio, but no texture or surface change in the carpet was observed. This study investigated low melt alloy fibers with modifications to their compositions (higher Technic "binder" and higher lactam concentrations).' The goal of the study was to find an alloy composition that would melt and bind fibers * together within a bundle during Superba® heatsetting. A primary requirement is that the composition must be melt spinnable and have acceptable fiber tensile properties. EXPERIMENTAL: The polymer blends were combined in a twin screw extruder and directly spun into fibers. The polymer melt temperature was at or below 218°C for all the blends evaluated, except for Sample #9, which was also run at 225°C. The finish emulsion was F-137-10 (Finish type F-137 with 10% Emulsion). The target Wet Pick Up (WPU) was 8% and the actual WPU was about 3.3-5.2%. The BCF host fiber is about 1100-]200 textured denier and is subsequently twisted to at least 5.75 tpi and Superba® textured prior to tufting. The following compositions were evaluated and spun into 25 denier/12 filaments and 50/12 fiber bundles, as shown in Table 6. (Table Remove) The binder fiber samples were inserted on a drawing and texturing machine into the host product (1123 mt) after drawing/texturing and before cominingling. The samples were Superba textured heatset at 258°C. Yarns were tested for plybonding and forwarded for conversion to a bonded carpet. OBSERVATIONS: CARPET AESTHETIC EVALUATION(TABLE REMOVE) The cut pile carpets were 8th gauge, the stitches per inch were 8, and the pile height was 22/32". The carpets were dyed and finished. The carpet bands were cut apart and subjectively evaluated for tips/texture and hand. The rankings were as follows: HAND EVALUATION: SOFTEST FIRMEST A1=B1 / Desirable } TIPS/TEXTURE EVALUATION: Low (WORST) HIGH (BEST) A1=B1 { Desirable } The best blend of hand and tips/texture appears close to those observed in samples A3 and B4. These results showed that nylon-6, nylon-6/6,6 and lactam can be blended together to form a multiphase fiber system and that when inserted into a host fiber and subsequently heatset yields carpets with varying degrees of hand and texture. The hand and tips/texture of the resultant carpets is a function of composition. Lactam concentration in the alloy mixture can have a significant negative effect on tenacity and ultimate elongation (UE). Tenacity and UE increase with decreasing lactam concentration. Concentrations at 10% or less appear most desirable with respect to fiber physical properties. The optimum mixture composition within the ranges evaluated was 78-82% binder polymer. 8-12% nylon-6 and FIBER MELTING PROPERTIES: Table 8 shows the experimental conditions for the Fiber Melting Tests, including showing each Sample ID (from Table 6 above). Table 9 shows the DSC results for each of these Sample IDs. There are two distinct polymer phases in the polyamide alloy as evidenced by two distinct melting points and multiple birefringence transitions. The shape and location of the melting peaks vary with composition and spinning melt temperature. Lactam concentration significantly effects the onset of melting of the binder polymer phase. The onset of melting of the binder phase decreases linearly as lactam concentration increased as observed in this Example and Figures 1-6. The ratio of lactarn/nylon-6 is highly correlated with melt point of the binder polymer phase. As the ratio increases above 1.5, the melt point of the binder phase decreases. This decrease in melt point is likely associated with a lactam phase and its solvation effect on the nylon-6 phase, which minimizes the co-polymerization of the two polyamide phases during melt processing. The sharpness of the melting peak (Tmeit-T0nset) of the binder polymer phase varies linearly with the lactam/binder polymer ratio. The binder phase melt peak broadens as the lactam/binder ratio increase. The number of plybonds stronger than the control yam (no binder) response increases (non-linearly) as the nylon/binder ratio decreases. The average force to pull the yarns apart also increases (non-linearly) as the nylon/binder ratio decreases. Increasing the bundle denier of the binder alloy in the host fiber increases the number of bonds and the mean force to pull the yarns apart, as expected. The lactam remaining in the fiber after extrusion is approximately 50% of the original amount added (over and above the lactam present in the original nylon-6 (MBM)). EXAMPLE 4 - ANOTHER CONTEMPLATED PRE-FIBER COMPOSITION FORMATION BACKGROUND: The previous study demonstrated sufficient melting and bonding of the binder alloy fibers through the Superba® HS process. The compositional effects on the fiber tensile properties and the melting/bonding properties of the binder alloy fibers are better understood through this and other Examples. EXPERIMENTAL: The polymer blends were combined in a twin screw extruder and directly spun into fibers. The polymer melt temperature was at or below 218°C for all the blends evaluated, except for Sample #9, which was also run at 225°C. The finish emulsion was F-137-10. The target Wet Pick Up (WPU) was 8% and the actual WPU was about 8-9%. The BCF host fiber is about 1100-1200 textured denier i and is subsequently twisted to at least 5.75 tpi and Superba® textured prior to tufting. The following compositions were evaluated and spun into 20 denier/6 filaments fiber bundles and are shown in Table 10 below: The binder fiber samples were inserted on a drawing and texturing machine into the 1202 mt after drawing/texturing and before commingling. The samples were Superba textured heatset at 258°C. Yarns were tested for pjybonding and forwarded for conversion to a bonded carpet. OBSERVATIONS: Lactaro concentration in the alloy mixture can have a significant negative effect on tenacity and ultimate elongation (C[E). Tenacity and VE increase with decreasing lactam concentration. Minimizing lactam concentration appears to be most desirable with respect to fiber physical properties. Ho wever> iactam concentration effects other melting properties and this impact should be considered when establishing the lactam target level. Note: sufficient lactarn is •equired at low spinning melt temperatures ( FIBER MELTING PROPERTIES: Tables 11-13 show the experimental conditions for the Fiber Melting Tests, including showing each Sample ID (from Table 10 above). Table 14 shows the DSC results for each of these Sample IDs. i There are two distinct polymer phases in the polyamide alloy as evidenced by two distinct melting points and multiple birefringence transitions. The shape and location of the melting peaks vary with composition and spinning melt temperature. Sample 9, shown below,, was sputa at 217°C and 225°C, which is slightly higher than the melt point of nylon-6. However, the DSC tests of this sample showed two distinct melting points and a sharper melting peak of the binder polymer phase with a reduced melting point. This result was unexpected, since we have observed that at melt temperatures around 260°C there is oniy one distinct polymer phase for a 50/50 Technic/nylon blend and melting point, in the absence of additional lactam. Lactam concentration significantly effects the onset of melting of the binder polymer phase. The onset of melting of the binder phase decreases linearly as lactam concentration increased as observed in this Example and Figures 7-16. The ratio of lactam/nylon-6 is highly correlated with melt point of the binder polymer phase. As the ratio increases above 1.5, the melt point of the binder phase decreases. This decrease in melt point is likely associated with a lactam phase. The sharpness of the melting peak (Tmcit-Tonset) of the binder polymer phase varies linearly with the lactam/binder polymer ratio. The binder phase melt peak broadens as the lactam/binder ratio increase. The number of plybonds stronger than the control yarn (no binder) response increases (non-1 inearly) as the nylon/binder ratio decreases. The average force to pull the yarns apart also increases (non-1 inearly) as the nylon/binder ratio decreases. Increasing the bundle denier of the binder alloy in the host fiber increases the number of bonds and the mean force to pull the yarns apart, as expected. EXAMPLE 5 - ANOTHER CONTEMPLATED PRE-FIBER COMPOSITION FORMATION BACKGROUND: Example 4 showed that the shape and location of the melting peaks may vary with spinning melt temperature, in addition to composition. Sample 9 from Example 4 was spun at 217°C and 225°C, which is slightly higher than the melt point of nylon-6. The DSC tests of this sample (#9B) showed 2 distinct melting points, which implies two distinct crystalline phases were present. This result was unexpected, since it has been observed mat at melt temperatures around 260°C there is onfy one distinct polymer phase at a 50/50-Technic/nyloa blend and one melting point, in the absence of additional lactam. EXPERIMENTAL: The polymer blends were combined in a twin screw extruder arid directly spun into fibers, The polymer melt temperature was varied between about 225°C and about 265°C. The BCF host fiber is about 1100-1200 textured denier and is subsequently twisted to at least 5.75 tpi and Superba® textured prior to tufting. The following compositions were evaluated and spun into 20 denier/6 filaments fiber bundles and are shown in Table 15 below: (TABLE REMOVE))OBSERVATIONS: Tenacity of the resulting fibers improves as the spinning melt temperature increases from 218°C to about 235DC with the composition evaluated. At temperatures greater 01 equal to about 235°C, tenacity remains constant and equal to the tenacity of the 100% binder (Technic) fibers. (See Figures 17-19). FIBER MELTING PROPERTIES: Tables 16-17 show the experimental conditions for the Fiber Melting Tests, including showing each Sample ID (from Table 15 above). Table 18 shows the DSC results for each of these Sample IDs. Increasing the spinning melt temperature doesn't significantly effect the melting behavior of the nylon or the binder (Technic) polymer phases. There were two distinct melting peaks in all of die samples evaluated between about TECHNIC PHASE ONSET MELTING °C TMELT °C 180.9 188.6 225°C and about 265°C. These results were unexpected. It was anticipated that co-poJyraerization would have taken place resuiting in a single polymer phase with one distinct melting point. The following data are averages of all of the samples evaluated, since there were no significant differences between the samples. Each sample was tested in duplicate. The values are in degrees C: NYLON-6 PHASE SAMPLE TMELT °C PREPARATION 216.1 DRIED PRIOR TO TESTING 110°C-16 HOURS 176.6 187.9 215.4 NONE-, TESTED AS • I RECEIVED Testing the samples as received prevents the formation of a low temperature melting peak at about 132-149°C. However, drying the fiber samples before DSC testing did not materially effect the melting point of either the Technic or nylon phases. The onset of melting of the Technic phase was slightly lower when the samples were tested as received. The multiphase fibers appear to have less gamma (y) crystalline structure as compared to the 100% Technic or 100% nylon-6 fibers. The XRD tests on sample 9F shows cd and a2 crystalline peaks (see Figure 20). EXAMPLE 6 - ANOTHER CONTEMPLATED PRE-FIBER COMPOSITION FORMATION BACKGROUND: Example 5 investigated the effect of spuming melt temperature on the resultant fiber melting and physical properties. The composition was held constant at 70% Technic, 25% nylon-6 and 5% lactam. Increasing the spinning melt temperature did not significantly effectithe melting behavior of the nylon or the binder (Technic) polymer phases. There were two distinct melting peaks in all of the samples evaluated between about 225°C and about 265°C. These results were unexpected. This Example shows if the presence of additional lactam is responsible for achieving multiple phase fibers spun at temperatures significantly higher than the melt point of either base polymer. This Example will establish the role that lactam plays in the phase separation of the two polymers and what is the minimum lactam level required to achieve phase separation during melt spinning. EXPERIMENTAL: The polymer blends were combined in a twin screw extruder and directly spun into fibers. The polymer melt temperature was varied between about 225°C and about 265°C. The BCF host fiber is about 1100-1200 textured denier and is subsequently twisted to at least 5.75 tpi and Superba® textured prior to tufting. , The following compositions were evaluated and spun into 20 denier/6 filaments fiber bundles and are shown in Table 19 belowTable Remove) The Technic/nylon-6 ratio was 2.8 for all of the above-referenced samples. OBSERVATIONS: Increasing lactam concentration has a negative effect on fiber physical properties as previously observed in Example 4. Increasing the melt temperature from about 245°C to about 265°C increases the % UE of the resultant fibers slightly, (see Figures 21-23) FIBER MELTING PROPERTIES: Tables 20-21 show the experimental conditions for the Fiber Melting Tests, including showing each Sample ID (from Table 19 above). Table 22 shows the DSC results for each of these Sample IDs. Removing excess lactam from the given compositional blend (Technic/nylon-6 ratio = 2.8) did not materially effect the melting point of either base polymer phase. Two distinct melt points were observed in the samples •without additional lactam at temperatures between about 245°C and about 265°C. EXAMPLE 7 - ANOTHER CONTEMPLATED FEE-FIBER COMPOSITION FORMATION BACKGROUND: Example 6 showed that removing excess lactam from the given compositional blend (Technic/nylon-6 ratio = 2.8) did not materially effect the melting point of either base polymer phase •within the lactam range evaluated. This Example looks at the compositional effects in the absence of additional lactam on the phase separation of the two base polymers as evidenced by two distinct melting points. EXPERIMENTAL: The polymer blends were combined in a twin screw extruder and directly spun into fibers. The polymer melt temperature was held constant at about 255°C. The BCF host fiber is about 1100-1200 textured denier and is subsequently twisted to at least 5,75 rpi and Superba® textured prior to tufting. The following compositions were evaluated and spun into 20 denier/6 filaments fiber bundles and are shown in Table 23 below; (TABLE REMOVE)OBSERVATIONS: Varying the Technia/Nylon ratio in the absence of additional lactam did not significantly effect the resultant fiber physical properties at spinning melt temperatures significantly higher than the melt point of either base polymer (255°C). The physical properties were very good and similar for all of the samples evaluated. FIBER MELTING PROPERTIES: Tables 24-25 show the experimental conditions for the Fiber Melting Tests, including showing each Sample ID (from Table 23 above). Table 26 shows'the DSC results for each of these Sample IDs. Two distinct melting points are observed at Technic (nylon-6,6,6 co-polymer) concentrations between about 40 and 75%. In this conventional melt blending of two polyamide polymers, the melt point of the low melt co-polymer (nylon-6,6,6) increases as the amount of the higher melt point polymer (nylon-6) increases, This observation can be attributed to co-polymerization that takes place during melt processing, (see Figure 24) The increase in melting point of the Technic phase varies linearly with Technic concentration in the absence of lactam. When combining previous data collected with this Example, it is evident that the incorporation of additional lactam decreases the melt point of the Techni The following regression equation was established using the current and previous compositions evaluated: TraC\|f(nyIon-6,6,6) = 159 + 0.190(% nylon-6,6,6) + 0.575(% nylon-6) - 2.35*(% lactam/% nyJon-6) Note: This equation accounts for over 87% of the variation in the melting point of the nylon-6,6,6 phase in the blend. I CRYSTALLINTY: The XRD analysis of selected samples shows the XRJJ patterns associated with the crystalline structure vary as a function of composition. More importantly, the addition of lactam to the mixture significantly changes the crystalline structure to more of an alpha structure (more stable) than the typical gamma crystalline form, which is common for this type of fiber and process. Sample 9F from Example 5 was included in the overlay graph for comparison. (See Figures 25-27). Thus, specific embodiments and applications of multiphase pre-fiber and fiber compositions and materials, their manufacture and uses thereof have been iisclosed. It should be apparent, however, to those skilled in the art that many nore modifications besides those already described are possible without departing rom the inventive concepts herein. The inventive subject matter, therefore, is not to be restricted except in the spirit of the disclosure. Moreover, in interpreting the disclosure, all terms should be interpreted in the broadest possible manner consistent with the context, hi particular, the terms 'comprises" and "comprising" should be interpreted as referring to elements, components, or steps in a nonexclusive manner, indicating that the referenced elements., components, or teps may he present, or utilized, or combined with other elements, components, or steps that are not expressly referenced. We claim 1. A spun fiber having at least two different melting points, which comprises a composition itself comprising: a first fiber constituent having a first melting point; a second fiber constituent having a second melting point, said second melting point different than said first melting point; one of said first and second fiber constituents present in said composition in an amount greater than the other of said first and second fiber constituents; and a gelling agent that solvates at least one of the first fiber constituent or the second fiber constituent, wherein the at least one gelling agent significantly reduces co-polymerization of the fiber constituents in the composition, and the at least one gelling agent comprises less than SO weight percent of the composition. 2. The spun fiber as claimed in claim 1, comprising at least one additional fiber constituent having a melting point that is different from the first melting point and the second melting point. 3. The spun fiber as claimed in claim 1, wherein at least one of the first fiber constituent and the second fiber constituent comprises at least one amide-based polymer. 4. The spun fiber as claimed in claim 3, wherein the at least one amide-based polymer comprises a nylon compound. 5. Thespun fiber as claimed in claim 4, wherein the nylon compound comprises nylon-6. 6. The spun fiber as claimed in claim 4, wherein the nylon compound comprises nylon-6,6. 7. The spun fiber as claimed in claim 4, wherein the nylon compound comprises a co¬polymer. 8. The spun fiber as claimed in claim 7, wherein the co-polymer comprises nylon-6,6,6. 9. The spun fiber as claimed in claim 1, wherein the at least one gelling agent comprises lactam. 10. The spun fiber as claimed in claim 9, wherein the lactam comprises caprolactam. 11. The spun fiber as claimed in claim 1, wherein the first fiber constituent comprises nylon 6,6,6, the second fiber constituent comprises nylon-6, and the gelling agent comprises a lactam-based compound. 12. The spun fiber as claimed in claim 1, wherein the at least one gelling agent comprises less than 40 weight percent of the composition. 13. The spun fiber as claimed in claim 1, wherein the at least one gelling agent comprises less than 30 weight percent of the composition. 14. The spun fiber as claimed in claim 1, wherein the at least one gelling agent comprises less than 20 weight percent of the composition. 15. The spun fiber as claimed in claim 1, wherein the at least one gelling agent comprises less than 10 weight percent of the composition. 16. The spun fiber as claimed in claim 1, wherein the at least one gelling agent comprises less than 5 weight percent of the composition. 17. The spun fiber as claimed in any of the preceding claims as and when used as a carpet product. 18. The spun fiber as claimed in claim 3, wherein each of the first fiber constituent and the second fiber constituent comprises at least one amide-based polymer. 19. A method of producing a spun fiber according to claim 1, comprising: providing a first fiber constituent having a first melting point; providing a second fiber constituent having a second melting point, wherein the first melting point and the second melting point are dissimilar; providing at least one gelling agent; mixing the first fiber constituent, the second fiber constituent and the at least one gelling agent to form a pre-fiber composition; and spinning the pre-fiber composition into a fiber. 20. The method as claimed in claim 19, comprising providing at least one additional fiber constituent having a melting point that is different from the first melting point and the second melting point. 21. The method as claimed in claim 19, wherein at least one of the first fiber constituent and the second fiber constituent comprises at least one amide-based polymer. 22. The method as claimed in claim 20, wherein the at least one amide-based polymer comprises a nylon compound. 23. The method as claimed in claim 22, wherein the nylon compound comprises nylon-6. 24. The method as claimed in claim 22, wherein the nylon compound comprises nylon 6,6.

Full Text

MULTIPHASE FIBER MATERIALS AJVD COMPOSITIONS, METHODS
OF MANUFACTURE AND USES THEREOF
LD OF THE SUBJECT MATTER
The field of the subject matter herein is multiphase pre-fiber and fiber materials and compositions, fiber products, yarn products and carpet products, methods of manufacture and uses thereof.
BACKGROUND
i
Fibers for consumer use, especially fibers that are incorporated into yams, carpet products and fabrics/textiles, are constantly being evaluated for improvements with respect to aesthetics and performance. These improvements may relate to appearance retention, texture and surface appearance, softness and floorweai performance. Fibers and fiber products are also being evaluated to determine if mere are more efficient and cost-effective manufacturing processes and equipment.
Fibers, •which can be used in the production of carpet products, such as wall-to-wall carpet, rugs and mats, are modified and in some instances improved to provide a certain yarn texture when they are incorporated into a carpet product and to provide a desired "look" for the space where the carpet product is being used. Additional issues that arise in the design of carpet fiber material and carpet products are daily and long-term performance and appearance.
One method that is being used to modify the texture of fabrics is to incorporate fibers mat have mixed deniers into the fabric product. Denier (or fibei denier) is a physical property of a particular fiber and can be defined as: "A direct yarn numbering measurement, it is die weight in grams of 9,000 meters of yarn. Therefore, the higher the denier, the larger the yarn. Typical nylon carpet fiber has 15-18 denier/filament." (see www.fabrica.com: Glossary of Fabric and Rug Terms) Another method that is being used to modify fibers and the resulting carpet or textile product is to incorporate not only fibers with mixed deniers, but also mixed lusters, such as the fiber and carpet product seen in commonly-owned

US Patent Application Serial No.: 10/602459, which is incorporated herein by reference in its entirety.
Another method of improving the aesthetics of carpet products that is related to the mixed denier method is to incorporate two fiber types - such as a low melt continuous (minority} fiber and a bulked continuous filament (BCF) host fiber. In order to create softer resultant carpets with improved tips, surface and texture, however, the concentration of the minority fiber needs to be reduced. The reduction in concentration of the low melt continuous minority fiber can be difficult because the concentration is ultimately limited by the denier of the minority fiber. In a conventional low melt/host fiber product, the low melt continuous fiber has a yarn denier of about 20-40 denier, and depending on the denier of the host fiber, the low melt fiber constituent can greatly influence the final properties of the resultant fiber and/or resultant carpet product. Traditionally, carpet yarn deniers range between 1000 and 1500.
Caprolactam and nylon compounds have each been individually polymerized with the same compounds (i.e. caprolactam/caprolactam or nylon/nylon) by anionic polymerization in a twin-screw extruder and then tested for residual monomer content and thermal/mechanical properties: however, in both processes, there were no mixed monomer anionic polymerization, the polymerization process did not result in a pre-fiber gel composition that could be processed by any means (including extrusion), there was no pre-fiber dispersion, and there is no indication that the mechanical strength or thermal strength was improved by the single monomer/twin-screw extruder mixing process, (see Antec '93 Conference Proceedings, New Orleans, 9th- 13th May 1993, Vol. 1, p. 470-473; and Antec '94 Conference Proceedings, San Francisco, CA, lsl-5* May 1994, Vol. 1, p. 116-22)
Therefore, it would be desirable to produce a multiphase pre-fiber and/or fiber material and/or composition that a) has sufficient viscosity and suitable melt strength such that it can be spun into a fiber or yam, b) can be processed by any processing method, including extrusion, c) can be incorporated into the production

of a fiber, yarn, textile and/or carpet product, d) allows for reduction of the .concentration of or the effect of the low melt material component without being constrained by a particular fiber denier, e) would comprise at least two dispersed constituents and exhibits at least two definitive and differentiatable melting points, and f) would produce a composition, fiber and/or product having tv/o melting points whereby the melt temperature of the constituent having the lower melting
point is maintained primarily by minimizing/preventing co-polymerization during
i
blending and processing steps, i
SUMMARY OF THE SUBJECT MATTER
A pre-fiber composition is disclosed herein that comprises: a) a first fiber constituent having a first melting point; b) a second fiber constituent having a second melting point; and c) a gelling agent that solvates at least one of the first fiber constituent or the second fiber constituent, wherein the gelling agent significantly reduces co-polymerization of either of the constituents in the composition.
A fiber is also disclosed herein'that comprises: a) at least two amide-based polymers, each having a melting point, wherein the melting point of one amide-based polymer is dissimilar to the melting point of a second amide-based polymer; and b) a gelling agent that is compatible with at least one of the amide-based polymers, wherein the fiber comprises two differentiatable melting points that are substantially similar to the melting points of each of the amide-based polymers.
A method of producing a pre-fiber composition is disclosed herein that comprises: a) providing a first fiber constituent having a first melting point; b) providing a second fiber constituent having a second melting point, wherein the first melting point and the second melting point are dissimilar; c) providing at least one gelling agent; and d) mixing the first constituent, the second constituent and the at least one gelling agent such that there is sufficient viscosity and sufficient melt strength in the composition so that it can be spun into a fiber and mch that the fust melting point and the second melting point in the fiber are substantially similar to their original values before mixing.

BRIEF DESCRIPTION OF THE FIGURES
Figure 1 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration.
Figure 2 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration,
Figure 3 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration.
Figure 4 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration.
Figure 5 shows data collected that relates to the onset of melting of the
binder phase and the lactam concentration.
t Figure 6 shows data collected that relates to the onset of melting of the
binder phase and the lactam concentration. '
Figure 7 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration,
Figure 8 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration.
Figure 9 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration.
Figure 10 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration.
Figure 11 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration.
Figure 12 shows data collected that relates to the onset of melting of the Dinder pha.se and the lactam concentration.
Figure 13 shows data collected that relates to the onset of melting of the jinder phase and the lactam concentration.

Figure 14 shows data collected that relates to the onset of melting of the . binder phase and the iactarn concentration.
Figure 15 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration.
Figure 16 shows data collected that relates to the onset of melting of the binder phase and the lactam concentration.
Figure 17 shows data collected that relates to fiber tenacity. i Figure 18 shows data collected that relates to fiber tenacity.
Figure 19 shows data collected that relates to fiber tenacity.
Figure 20 shows XRD data collected for a contemplated embodiment of the subject matter herein.
Figure. 21 shows data collected that relates to the %UE of a contemplated embodiment of the subject matter herein.
Figure 22 shows data collected that relates to the %UE of a contemplated embodiment of the subject matter herein.
Figure 23 shows data collected that relates to the %UE of a contemplated
embodiment of the subject matter herein.
i
Figure 24 shows data collected that relates to the melting point versus the Tecliriic concentration in a contemplated embodiment of the subject matter herein.
Figure 25 shows XRD data collected for a contemplated embodiment of the subject matter herein.
Figure 26 shows XRD data collected for a contemplated embodiment of
the subject matter herein.
Figure 27 shows XRD data collected for a contemplated embodiment of the subject matter herein.

DETAILED DESCRIPTION
A multiphase pre-fiber and/or fiber material and/or composition has been produced that a) has sufficient viscosity and suitable melt strength such that it can be spun into a fiber or yarn, b) can be processed by any processing method,, including extrusion, c) can be incorporated into the production of a fiber, yarn, textile and/or carpet product, d) allows for reduction of the concentration of or the effect of the low melt material component without being constrained by a .particular fiber denier, e) comprises at least two dispersed constituents and exhibits at least two definitive and differentiatable melting points, and f) can produce a composition, fiber and/or product having at least two constituents each with a different melting point whereby the melt temperature of the constituent having the lower melting point is maintained primarily by minimizing/preventing co-polymerization during blending and processing steps. These pre-fiber and fiber materials and/or compositions at temperatures are also able to be processed at or below normal processing temperatures for a nylon fiber product.
Tn some embodiments, there is a formation of a multiphase pre-fiber and/or fiber gel-spun composition and/or material that allows for the control of the properties of the drawn liber by allowing for more favorable orientation of the polymer molecules in the fiber. Controlling the molecule orientation can lead to increased tensile strength and an overall fiber improvement in the fiber physical properties. Furthermore, at least part of the at least one gelling agent can be removed and recovered from the spun fiber once formed. Formation of one of the embodiments - the pre-fiber gel composition - is also described in commonly-owned US Utility Application entitled "Pre-fiber Gel Materials and Compositions, Methods of Manufacture and Uses Thereof (Serial No. not yet assigned) that has been filed concurrently and is incoiporated herein in its entirety by reference.
In order to produce a pre-fiber composition, dispersion and/or material that can be formed into a gel spun fiber, a contemplated pre-fiber composition includes, a) a first fiber constituent having a first melting point: b) a second fiber constituent having a second melting point; and c) a gelling agent that solvates at

least one of the first fiber constituent or the 'second fiber constituent while at the same time minimizing and/or preventing co-polymerization of the first constituent with the second constituent or either of the individual components with itself (for example, first constituent-first constituent intermolecular or intramolecular polymerization). In other embodiments, the addition of the at least one gelling agent forms a gel composition that has sufficient viscosity and sufficient melt
strength upon the mixing of the first fiber constituent, the second fiber constituent
i and the at least one gelling agent that the composition can be spun into a fiber.
i
At this point it should be understood that, unless otherwise indicated, all numbers expressing quantities of ingredients, constituents, interaction conditions and so forth used in the specification and claims are to be understood as being* modified in all instances by the term "about". Accordingly, unless indicated to the contrary, the numerical parameters set forth in the specification and attached claims are approximations that may vary depending upon the desired properties sought to be obtained by the subject matter presented herein. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the subject matter presented herein are approximations., the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contain certain errors ' necessarily resulting from the standard deviation found in then- respective testing measurements.
A first fiber constituent and a second fiber constituent are the starting points for the formation of a pre-fiber composition, dispersion and/or material, and the mixture of the two can be characterized as a "binder alloy fiber" or an "alloy mixture". It should be understood that the first fiber constituent and the second fiber constituent may comprise any suitable monomer, polymer or moiety, as long as each individual or both combined constituents is capable of being used

as a fiber material, especially in yarn products, fabric/textile products and/or carpet products.
In one embodiment, the first fiber constituent may comprise at least one amide-based compound and/or polyamide-based compound and the second liber constituent may comprise at least one second amide-based compound and/or polyamide-based compound. As used herein, the term "compound" means a substance with constant composition that can be broken down into elements by chemical processes. Polyamides and polyamide-based compounds, as the name implies, are polymers that comprise amide monomers. Several contemplated polyamide-based compounds comprise nylon-6, nylon-6,6, "nylon-6,6,6" (uylon-6/nyIon-6,6 copolymer) and/or nylon-12.
Amides are an important group of nitrogenous compounds and monomers that are used as intermediates and/or building blocks in the production of polymers, textiles, plastics and adhesives. Amide monomers are generally' represented by the following formula:
O
II RCNH
wherein R is an alkyl group, an aryl group, a cyclic allcyl group, an alkenyl group, an arylalkylene group, or any other appropriate group that can be utilized to be a part of an amide compound.
As used herein, the term "monomer" generally refers to any chemical compound that is capable of forming a covalent bond with itself or a chemically iifferent compound in a repetitive manner. The repetitive bond formation between aionomers may lead to a linear, branched, super-branched, or three-dimensional product. Furthermore, monomers may themselves comprise repetitive building blocks, and when polymerized the polymers formed from such monomers are then

termed "blockpolymers'". The weight-average molecular weight of monomers may vary greatly between about 40 Dalton and 20000 Dalton. However, especially when monomers comprise repetitive building blocks., monomers may have even higher molecular weights. Monomers may also include additional groups, such as groups used for crosslinking, radiolabeling. and/or chemical or environmental protecting.
The term "alkyl" is used herein to mean a branched or a straight-chain
saturated hydrocarbon group or substituent of 1 to 24 carbon atoms, such as
i
methyl, ethyl, n-propyl. isopropyl, n-butyl, isobutyl, t-butyl, octyl, decyl, tetradecyl, hexadecyl. eicosyl, tetracosyl and the like. In some embodiments, contemplated alkyl groups contain 1 to 12 carbon atoms. The term "cyclic alkyl" means an alkyl compound whose structure is characterized by one or more closed rings. The cyclic alkyl may be mono-, bi-, tri- or polycyclic depending on the number of rings present in the compound. The term "aryl" is used herein to mean a monocyclic aromatic species of 5 to 7 carbon atoms or a compound that is buiit with monocyclic aromatic species of 5 to 7 carbon atoms and is typically phenyl, naphthalyl, phenanthryl, anthracyl etc. Optionally, these groups are substituted with one to four, more preferably one to two alkyl. alkoxy, hydroxy, and/or nitro
substituents.
i The term "alkenyl" is used herein to mean a branched or a straight-chain
hydrocarbon chain containing from 2 to 24 carbon atoms and at least one double bond. Preferred alkenyl groups herein contain 1 to 12 carbon atoms. The term "alkoxy" is used herein to mean an alkyl group bound through a single, terminal ether linkage; that is, an alkoxy group may be defined as -OR wherein R is an alley) group, as defined above. The term "arylalkylene" is used herein to mean moieties containing both alkylene and monocyclic aryl species, typically containing less than about 12 carbon atoms in the alkylene portion, and wherein the aryl substituent is bonded to the structure of interest tlirough an alkylene [inking group. Exemplary arylalkylene groups have the structure -(CH2)j-Ar wherein "j" is an integer in the range of 1 to 6 and wherein "Ar" is an aryl species.

. The first fiber constituent comprises a first melting point and the second fiber constituent has a second melting point, and it should be understood that the first melting point and the second melting point are different from one another. Melting points can be determined by any available method, including differential scanning calorimetry (DSC), which is used herein and shown in the Examples section. It should further be understood that these at least two melting points are found in the same pre-fiber composition and/or the same fiber before the fiber is formed and after the fiber is formed/spun.
In additional embodiments, at least one additional fiber constituent may be
added to the pre-fiber composition and/or dispersion, wherein the at least one
additional fiber constituent has at least one additional melting point that is
measurably different from both the first melting point and the second melting
point. >
At least one gelling agent is provided mat is mixed and/or blended with the first or second fiber constituent, the at least one poiyamide-based or the at least one amide-based compound in order to fonn a contemplated pre-fiber composition and/or dispersion. The at least one gelling agent may comprise any suitable solvent that a) can solvate and is compatible with either the first or the second fiber constituent and b) is at least partially compatible with the other fiber constituents) in the pre-fiber composition. As mentioned, a suitable gelling agent is one that is compatible with either the first or the second fiber constituent. The term "compatible" means mat gelling agent that does not contribute any negative effects to the pre-fiber composition, such as by making one of the constituents "watery", by reacting with either the first or second fiber constituent (or additional constituents), by making the dispersion "non-spinnable", by making the "low melt" constituent into a composition that does not retain its low melting point, by inducing co-polymerization in the dispersion between or among any of the constituents and combinations of any of these negative effects thereof.
In some embodiments, especially those embodiments where the first fiber constituent and the second fiber constituent comprise amide-based compounds.

the getting agent comprises a iactam. It should be understood that lactam is a . suitable gelling agent because, in the embodiments where the first fiber constituent and the second fiber constituent comprise amide-based compounds, lactam is very compatible with at least one of the first fiber constituent or the second fiber constituent and is at least partially compatible with the other fiber constiruent(s).
In yet other embodiments, the lactam-based gelling agent comprises a caprolactam, such as e-caprolactam. s-Caprolactam, also known as aminocaproic lactam and 2-oxohexamethyleneirnme, is a compound that is produced in flake and molten forms and is used primarily in the manufacture of nylon-6 and nylon-6,6,6 products such as those products contemplated herein or other synthetic fibers, plastics, bristles, films, coatings, synthetic leathers, plasticizers and paint vehicles. Caprolactam can also be used as a cross-linking agent for polyurethanes and in the synthesis of the amino acid lysine. A contemplated lactam preparation method is shown herein in Example 1.
Amides, such as caprolactam, can also be produced by reacting a ketone with hydroxylamine to make an oxime, and then using an acid catalyzed rearrangement of the oxime(s), conventionally called the Beckmann
rearrangement, to form the amide. Merchant quality caprolactam can be produced
i
by methods described in US Patent Application Serial No.: 10/251335 filed on September 21, 2002, which is commonly owned and herein incorporated in its entirety.
The at least one gelling agent may be added in any suitable weight percentage with respect to the other composition/dispersion constituents, as long as the addition of the gelling agent aids in the production of a pre-fiber composition/dispersion. In a contemplated embodiment, the at least one gelling agent comprises less than 50 weight percent of the composition/dispersion. In another contemplated embodiment, the at least one gelling agent comprises less than 40 weight percent of the composition/dispersion. In yet another contemplated embodiment, the at least one gelling agent comprises less than 30

weight percent of the composition/dispersion. In other contemplated embodiments, the at least one gelling agent comprises less than 20 weight percent of the composition/dispersion. In yet other contemplated embodiments, the at least one gelling agent comprises less than 10 weight percent of the composition/dispersion. Also, in some contemplated embodiments, the at least one gelling agent comprises less than 5 weight percent of the composition/dispersion.
Once the pre-fiber composition/dispersion is formed, the composition/dispersion may be extruded through a suitable die or spinnerette for production of a "minority" fiber. It should be understood that the resulting fiber will comprise the first fiber constituent having and retaining a first melting point (at or near its original melting point) and the second fiber constituent having and retaining a second melting point (at or near its original melting point), whereby co-polymerization between any or all of the constituents has been minimized and/or prevented entirely through the addition of the gelling agent. The minority fiber may then be combined with a "host" fiber or bulked continuous filament (BCF) "host" fiber to create a carpet product mat is softer than conventional carpet products made with conventional low melt fiber comprising 100% low melt co-polymer and that comprises improved tips, surface and texture, as opposed to conventional carpet products made without the addition of low melt fibers. These conventional melt-blended polymer fibers generally comprise significant and undesirable co-polymerization, such that the melt point of the low melt polymer increases as the amount of the higher melt point polymer increases. These fibers will not melt and bond at the temperature of the original low melt polymer and hence not effect the aesthetics of the resultant carpets if heat treated at the same temperature.
In addition, a method of producing a pre-fiber composition and/or dispersion includes: a) providing a first fiber constituent having a first melting point; b) providing a second fiber constituent having a second melting point, wherein the first melting point and the second melting point are dissimilar; c) providing at least one gelling agent: and d) mixing the first fiber constituent, the

second liber coJisuiusru ana me at least one' gelling agent such that there is .sufficient viscosity and sufficient melt strength in the composition so that it can be spun into a fiber while at the same time minimizing and/or preventing co-polyinerization between any of the constituents. Once the pre-fiber composition and/or dispersion is formed, it can be formed into a fiber, which can in turn be combined with a host fiber to form a yarn and then a carpet product having
improved tips, surface and texture.
i
The first fiber constituent, the second fiber constituent, the at least one gelling agent and/or the at least one additional constituent and/or gelling agent may be provided by any suitable method, including a) buying at least some of the first fiber constituent, the second fiber constituent, the at least one gelling agent and/or the at least one additional constituent and/or gelling agent from a supplier or textile mill; b) preparing or producing at least some of the first fiber constituent, the second fiber constituent, the at least one gelling agent and/or the at least one additional constituent and/or gelling agent in house using chemicals provided by another source and/or c) preparing or producing at least some of the first fiber constituent, the second fiber constituent, the at least one gelling agent and/or the at least one additional constituent and/or gelling agent in house using chemicals also produced or provided in house or at the location.
!
During or after the formation of contemplated pre-fiber compositions, gel-spun fiber materials, yarn products and/or carpet products, a thermal energy may be applied to the materials and/or products, wherein the thermal energy comprises a temperature that is below, at or above the melting point of the higher melting point constituent, the fiber and/or other heat-active components. The thermal energy can be applied to activate at least some of the plurality of fibers. In some embodiments, activating the fibers comprises forming chemical, such as covalent, ionic or hydrogen and/or physical, such as adhesion, bonds between at least some of the plurality of fibers and at least one of the other components. It should be understood, however, that the thermal energy will not induce co-polymerization between any of the constituents in the minority fiber or pre-fiber composition. It should also be understood that regardless of the temperature of the thermal energy

that is applied - whether its below, at or above the melting point of the higher melting fiber constituent - the pre-fiber composition and/or fiber product continues to maintain at least two distinct and differentiatable melting points.
The thermal energy may come from any suitable source, including extended/non-point sources, such as a UV-VIS source, an infra-red source, a heat source, both radiative and convective. or a microwave source; or electron sources, such as electron guns or plasma sources. Other suitable energy sources include electron beams, and radiative devices at non-IR wavelengths including x-ray, and gamma ray. Still other suitable energy sources include vibrational sources such as microwave transmitters. In preferred embodiments, the energy source is an extended source. In more preferred embodiments, the energy source is a heat source, such as an atmospheric pressure forced air machine, which can be followed by a steam purge, or a pressurized twist-setting machine. An example of ail atmospheric pressure forced air machine is the Suessen® Twist-Setting , Machine. Examples of pressurized twist-setting machines are those of the autoclave-type and those manufactured by Superba®.
It should be understood that the thermal energy may be applied consistently or in short bursts. It is also contemplated that the thermal energy may be gradually and continuously applied over a temperature range until the thermal energy is at or above the melting point of the fiber or other heat-active components. For example, the fiber material and/or yarn may be heated by an atmospheric pressure forced air machine at a temperature of about 195°C for a residence time of about 60 seconds, before the treated fiber material and/or yarn product is tufted. The thermal energy may also be immediately applied at or above the melting point of the binder fiber and/or other heat-active components without any ramp time. It should also be understood that the temperature at which the low melt polymer phase melts is generally dependent on the atmospheric conditions. For example, the melt point of polyamides are depressed in the presence of water.

The pre-fiber materials contemplated and described herein may be used . alone or in combination with oilier materials and/or products to form any suitable product, including a spun fiber product, a yam product, a fabric product and/or a carpet product.
EXAMPLES
The pre-fiber composition, spun and gel-spun fiber materials, yam products, carpet products and methods used to product those materials and products, as described in the examples, are for illustrative purpose only and should not, in any way, limit the scope of this invention.
EXAMPLE 1 - L ACT AM PREPARATION
Four liters of caprolactam were melted in a convection oven overnight in a covered container. The lactam was poured into a 5L 3-necked distillation flask with a magnetic stir bar and an electric heating mantle (top and bottom mantles). The distillation column was vacuum jacketed by a 29/42 column and a 10 tray-section, a 5 tray section, a splitting distillation head and a condenser. The condenser was held at 50°C with a heated water circulator. The system had the pressure reduced from 7 mm Hg to 4 mm Hg. Heat was applied and the column was brought to reflux conditions and held for 30 minutes. After 30 minutes for the column to stabilize, the distillation head splitter was activated with a 4 second take off and a 10 second reflux. Slightly less than 1 liter-of lactam was distilled off. The heat was turned off and the mantles were removed allowing the lactam in the 5-liter flask to drop to 90UC before breaking the vacuum on the system. The 5-liter flask was removed and the lactam was poured into 1 -liter nalgene beakers and promptly placed into a glove box with a dry nitrogen atmosphere. After cooling overnight, the crystal lactam was transferred to plastic bags and was broken into flake form with a hammer inside the glove box. The lactam was stored inside the dry glove box under house nitrogen until needf-d for the pre-fiber gel composition formation.

EXAMPLE: 2 - A CONTEMPLATED PRE-FIBER GEL COMPOSITION FORMATION
Nylon-6 was ground to a fine powder and mixed with a lactam gelling agent, which was in this case - caprolactam. A Braybender rnixer was used to mix the nylon and caprolactam at a speed of 60 RPM. Addition time took about 5 minutes and the gd was allowed to mix for 15 minutes after charging at the temperature indicated. The samples were removed while the Braybender was running with a brass wipe stick. The samples were then ground in a Willey mill using a course screen. A weighted amount of each ground gel mix was extracted 16+ hours using a jacketed soxlet extractor. The extract was filtered using a folded #54 paper and rinsed into a 100 mL volumetric flask. The extract was brought to volume with deionized water and then analyzed by Gas Chromatography for % lactam using a Carbowax column.(Table Remove)
The resulting gels were geJ spun orr an twin screw extruder. The gels spun into a fiber product surprisingly well and packages of liber were able to be prepared at most conventional spinning conditions. Furthermore, it was observed that extruder temperature could be dropped below conventional conditions for neat polymers, given that the gel compositions allowed for lower extruder pressures. Tables 1-5. shown below, give summaries of several of the spinning
conditions utilized in these Examples.
i
EXAMPLE 3 - A CONTEMPLATED PRJE-FIBER COMPOSITION FORMATION
i
BACKGROUND:
Conventional binder alloy samples (1-end of 22 denier/12 fils) were inserted into 1202 mp 2-ply yarns during cabling and Supeiba® heatset. Plybond tests of the yarns did not show any evidence of bonding after Superba® heatset. Subsequently, we autoclave heatset the yams followed by conversion into a banded carpet. No significant aesthetic effect in the carpet was observed with any of the conventional binder alloy samples. However, there was a slight impact (firmness) on carpet hand at the lowest nylon/binder ratio, but no texture or surface change in the carpet was observed.
This study investigated low melt alloy fibers with modifications to their compositions (higher Technic "binder" and higher lactam concentrations).' The goal of the study was to find an alloy composition that would melt and bind fibers
*
together within a bundle during Superba® heatsetting. A primary requirement is that the composition must be melt spinnable and have acceptable fiber tensile
properties.
EXPERIMENTAL:
The polymer blends were combined in a twin screw extruder and directly spun into fibers. The polymer melt temperature was at or below 218°C for all the blends evaluated, except for Sample #9, which was also run at 225°C. The finish emulsion was F-137-10 (Finish type F-137 with 10% Emulsion). The target Wet Pick Up (WPU) was 8% and the actual WPU was about 3.3-5.2%. The BCF host

fiber is about 1100-]200 textured denier and is subsequently twisted to at least 5.75 tpi and Superba® textured prior to tufting.
The following compositions were evaluated and spun into 25 denier/12 filaments and 50/12 fiber bundles, as shown in Table 6.

(Table Remove)
The binder fiber samples were inserted on a drawing and texturing machine into the host product (1123 mt) after drawing/texturing and before cominingling. The samples were Superba textured heatset at 258°C. Yarns were tested for plybonding and forwarded for conversion to a bonded carpet.
OBSERVATIONS:
CARPET AESTHETIC EVALUATION(TABLE REMOVE)

The cut pile carpets were 8th gauge, the stitches per inch were 8, and the pile height was 22/32". The carpets were dyed and finished. The carpet bands were cut apart and subjectively evaluated for tips/texture and hand. The rankings were as follows:
HAND EVALUATION:
SOFTEST FIRMEST
A1=B1 / Desirable }
TIPS/TEXTURE EVALUATION:
Low (WORST) HIGH (BEST)
A1=B1 { Desirable }
The best blend of hand and tips/texture appears close to those observed in samples A3 and B4. These results showed that nylon-6, nylon-6/6,6 and lactam can be blended together to form a multiphase fiber system and that when inserted into a host fiber and subsequently heatset yields carpets with varying degrees of hand and texture. The hand and tips/texture of the resultant carpets is a function of composition.
Lactam concentration in the alloy mixture can have a significant negative effect on tenacity and ultimate elongation (UE). Tenacity and UE increase with decreasing lactam concentration. Concentrations at 10% or less appear most desirable with respect to fiber physical properties. The optimum mixture composition within the ranges evaluated was 78-82% binder polymer. 8-12% nylon-6 and FIBER MELTING PROPERTIES:
Table 8 shows the experimental conditions for the Fiber Melting Tests, including showing each Sample ID (from Table 6 above). Table 9 shows the DSC results for each of these Sample IDs.
There are two distinct polymer phases in the polyamide alloy as evidenced by two distinct melting points and multiple birefringence transitions. The shape and location of the melting peaks vary with composition and spinning melt temperature.
Lactam concentration significantly effects the onset of melting of the binder polymer phase. The onset of melting of the binder phase decreases linearly as lactam concentration increased as observed in this Example and Figures 1-6.
The ratio of lactarn/nylon-6 is highly correlated with melt point of the binder polymer phase. As the ratio increases above 1.5, the melt point of the binder phase decreases. This decrease in melt point is likely associated with a lactam phase and its solvation effect on the nylon-6 phase, which minimizes the co-polymerization of the two polyamide phases during melt processing.
The sharpness of the melting peak (Tmeit-T0nset) of the binder polymer phase varies linearly with the lactam/binder polymer ratio. The binder phase melt peak broadens as the lactam/binder ratio increase.
The number of plybonds stronger than the control yam (no binder) response increases (non-linearly) as the nylon/binder ratio decreases. The average force to pull the yarns apart also increases (non-linearly) as the nylon/binder ratio decreases. Increasing the bundle denier of the binder alloy in the host fiber increases the number of bonds and the mean force to pull the yarns apart, as expected.
The lactam remaining in the fiber after extrusion is approximately 50% of the original amount added (over and above the lactam present in the original nylon-6 (MBM)).
EXAMPLE 4 - ANOTHER CONTEMPLATED PRE-FIBER COMPOSITION FORMATION
BACKGROUND:
The previous study demonstrated sufficient melting and bonding of the binder alloy fibers through the Superba® HS process. The compositional effects on the fiber tensile properties and the melting/bonding properties of the binder alloy fibers are better understood through this and other Examples.
EXPERIMENTAL:
The polymer blends were combined in a twin screw extruder and directly spun into fibers. The polymer melt temperature was at or below 218°C for all the blends evaluated, except for Sample #9, which was also run at 225°C. The finish emulsion was F-137-10. The target Wet Pick Up (WPU) was 8% and the actual
WPU was about 8-9%. The BCF host fiber is about 1100-1200 textured denier
i
and is subsequently twisted to at least 5.75 tpi and Superba® textured prior to tufting.
The following compositions were evaluated and spun into 20 denier/6 filaments fiber bundles and are shown in Table 10 below:

The binder fiber samples were inserted on a drawing and texturing machine into the 1202 mt after drawing/texturing and before commingling. The samples were Superba textured heatset at 258°C. Yarns were tested for pjybonding and forwarded for conversion to a bonded carpet.
OBSERVATIONS:
Lactaro concentration in the alloy mixture can have a significant negative effect on tenacity and ultimate elongation (C[E). Tenacity and VE increase with decreasing lactam concentration. Minimizing lactam concentration appears to be most desirable with respect to fiber physical properties. Ho wever> iactam concentration effects other melting properties and this impact should be considered when establishing the lactam target level. Note: sufficient lactarn is •equired at low spinning melt temperatures ( FIBER MELTING PROPERTIES:
Tables 11-13 show the experimental conditions for the Fiber Melting Tests, including showing each Sample ID (from Table 10 above). Table 14
shows the DSC results for each of these Sample IDs.
i There are two distinct polymer phases in the polyamide alloy as evidenced
by two distinct melting points and multiple birefringence transitions. The shape and location of the melting peaks vary with composition and spinning melt temperature. Sample 9, shown below,, was sputa at 217°C and 225°C, which is slightly higher than the melt point of nylon-6. However, the DSC tests of this sample showed two distinct melting points and a sharper melting peak of the binder polymer phase with a reduced melting point. This result was unexpected, since we have observed that at melt temperatures around 260°C there is oniy one

distinct polymer phase for a 50/50 Technic/nylon blend and melting point, in the absence of additional lactam.
Lactam concentration significantly effects the onset of melting of the binder polymer phase. The onset of melting of the binder phase decreases linearly as lactam concentration increased as observed in this Example and Figures 7-16.
The ratio of lactam/nylon-6 is highly correlated with melt point of the binder polymer phase. As the ratio increases above 1.5, the melt point of the binder phase decreases. This decrease in melt point is likely associated with a lactam phase. The sharpness of the melting peak (Tmcit-Tonset) of the binder polymer phase varies linearly with the lactam/binder polymer ratio. The binder phase melt peak broadens as the lactam/binder ratio increase.
The number of plybonds stronger than the control yarn (no binder) response increases (non-1 inearly) as the nylon/binder ratio decreases. The average force to pull the yarns apart also increases (non-1 inearly) as the nylon/binder ratio decreases. Increasing the bundle denier of the binder alloy in the host fiber increases the number of bonds and the mean force to pull the yarns apart, as expected.
EXAMPLE 5 - ANOTHER CONTEMPLATED PRE-FIBER COMPOSITION FORMATION
BACKGROUND:
Example 4 showed that the shape and location of the melting peaks may vary with spinning melt temperature, in addition to composition. Sample 9 from Example 4 was spun at 217°C and 225°C, which is slightly higher than the melt point of nylon-6. The DSC tests of this sample (#9B) showed 2 distinct melting points, which implies two distinct crystalline phases were present. This result was unexpected, since it has been observed mat at melt temperatures around 260°C there is onfy one distinct polymer phase at a 50/50-Technic/nyloa blend and one melting point, in the absence of additional lactam.

EXPERIMENTAL:
The polymer blends were combined in a twin screw extruder arid directly spun into fibers, The polymer melt temperature was varied between about 225°C and about 265°C. The BCF host fiber is about 1100-1200 textured denier and is subsequently twisted to at least 5.75 tpi and Superba® textured prior to tufting.
The following compositions were evaluated and spun into 20 denier/6 filaments fiber bundles and are shown in Table 15 below:

(TABLE REMOVE))OBSERVATIONS:
Tenacity of the resulting fibers improves as the spinning melt temperature increases from 218°C to about 235DC with the composition evaluated. At temperatures greater 01 equal to about 235°C, tenacity remains constant and equal to the tenacity of the 100% binder (Technic) fibers. (See Figures 17-19).
FIBER MELTING PROPERTIES:
Tables 16-17 show the experimental conditions for the Fiber Melting Tests, including showing each Sample ID (from Table 15 above). Table 18 shows the DSC results for each of these Sample IDs.
Increasing the spinning melt temperature doesn't significantly effect the melting behavior of the nylon or the binder (Technic) polymer phases. There were two distinct melting peaks in all of die samples evaluated between about

TECHNIC PHASE
ONSET MELTING °C TMELT °C
180.9 188.6
225°C and about 265°C. These results were unexpected. It was anticipated that co-poJyraerization would have taken place resuiting in a single polymer phase with one distinct melting point. The following data are averages of all of the samples evaluated, since there were no significant differences between the samples. Each sample was tested in duplicate. The values are in degrees C:
NYLON-6 PHASE SAMPLE
TMELT °C PREPARATION
216.1 DRIED PRIOR
TO TESTING
110°C-16
HOURS
176.6 187.9 215.4 NONE-,
TESTED AS •
I
RECEIVED
Testing the samples as received prevents the formation of a low temperature melting peak at about 132-149°C. However, drying the fiber samples before DSC testing did not materially effect the melting point of either the Technic or nylon phases. The onset of melting of the Technic phase was slightly lower when the samples were tested as received.
The multiphase fibers appear to have less gamma (y) crystalline structure as compared to the 100% Technic or 100% nylon-6 fibers. The XRD tests on sample 9F shows cd and a2 crystalline peaks (see Figure 20).
EXAMPLE 6 - ANOTHER CONTEMPLATED PRE-FIBER COMPOSITION FORMATION
BACKGROUND:
Example 5 investigated the effect of spuming melt temperature on the resultant fiber melting and physical properties. The composition was held constant at 70% Technic, 25% nylon-6 and 5% lactam. Increasing the spinning melt temperature did not significantly effectithe melting behavior of the nylon or the binder (Technic) polymer phases. There were two distinct melting peaks in all of the samples evaluated between about 225°C and about 265°C. These results were unexpected. This Example shows if the presence of additional lactam is responsible for achieving multiple phase fibers spun at temperatures significantly higher than the melt point of either base polymer. This Example will establish the role that lactam plays in the phase separation of the two polymers and what is the minimum lactam level required to achieve phase separation during melt spinning.
EXPERIMENTAL:
The polymer blends were combined in a twin screw extruder and directly spun into fibers. The polymer melt temperature was varied between about 225°C and about 265°C. The BCF host fiber is about 1100-1200 textured denier and is subsequently twisted to at least 5.75 tpi and Superba® textured prior to tufting.
, The following compositions were evaluated and spun into 20 denier/6 filaments fiber bundles and are shown in Table 19 belowTable Remove)
The Technic/nylon-6 ratio was 2.8 for all of the above-referenced samples. OBSERVATIONS:
Increasing lactam concentration has a negative effect on fiber physical properties as previously observed in Example 4. Increasing the melt temperature from about 245°C to about 265°C increases the % UE of the resultant fibers slightly, (see Figures 21-23)
FIBER MELTING PROPERTIES:
Tables 20-21 show the experimental conditions for the Fiber Melting Tests, including showing each Sample ID (from Table 19 above). Table 22 shows the DSC results for each of these Sample IDs.
Removing excess lactam from the given compositional blend (Technic/nylon-6 ratio = 2.8) did not materially effect the melting point of either base polymer phase. Two distinct melt points were observed in the samples •without additional lactam at temperatures between about 245°C and about 265°C.
EXAMPLE 7 - ANOTHER CONTEMPLATED FEE-FIBER COMPOSITION FORMATION
BACKGROUND:
Example 6 showed that removing excess lactam from the given compositional blend (Technic/nylon-6 ratio = 2.8) did not materially effect the melting point of either base polymer phase •within the lactam range evaluated. This Example looks at the compositional effects in the absence of additional lactam on the phase separation of the two base polymers as evidenced by two distinct melting points.
EXPERIMENTAL:
The polymer blends were combined in a twin screw extruder and directly spun into fibers. The polymer melt temperature was held constant at about 255°C. The BCF host fiber is about 1100-1200 textured denier and is subsequently twisted to at least 5,75 rpi and Superba® textured prior to tufting.

The following compositions were evaluated and spun into 20 denier/6 filaments fiber bundles and are shown in Table 23 below;

(TABLE REMOVE)OBSERVATIONS:
Varying the Technia/Nylon ratio in the absence of additional lactam did not significantly effect the resultant fiber physical properties at spinning melt temperatures significantly higher than the melt point of either base polymer (255°C). The physical properties were very good and similar for all of the samples evaluated.
FIBER MELTING PROPERTIES:
Tables 24-25 show the experimental conditions for the Fiber Melting Tests, including showing each Sample ID (from Table 23 above). Table 26 shows'the DSC results for each of these Sample IDs.
Two distinct melting points are observed at Technic (nylon-6,6,6 co-polymer) concentrations between about 40 and 75%. In this conventional melt blending of two polyamide polymers, the melt point of the low melt co-polymer (nylon-6,6,6) increases as the amount of the higher melt point polymer (nylon-6) increases, This observation can be attributed to co-polymerization that takes place during melt processing, (see Figure 24) The increase in melting point of the Technic phase varies linearly with Technic concentration in the absence of lactam.
When combining previous data collected with this Example, it is evident that the incorporation of additional lactam decreases the melt point of the Techni The following regression equation was established using the current and previous compositions evaluated:
TraC|f(nyIon-6,6,6) = 159 + 0.190*(% nylon-6,6,6) + 0.575*(% nylon-6) - 2.35*(% lactam/% nyJon-6)
Note: This equation accounts for over 87% of the variation in the melting point of the nylon-6,6,6 phase in the blend.
I
CRYSTALLINTY:
The XRD analysis of selected samples shows the XRJJ patterns associated with the crystalline structure vary as a function of composition. More importantly, the addition of lactam to the mixture significantly changes the crystalline structure to more of an alpha structure (more stable) than the typical gamma crystalline form, which is common for this type of fiber and process. Sample 9F from Example 5 was included in the overlay graph for comparison. (See Figures 25-27).
Thus, specific embodiments and applications of multiphase pre-fiber and fiber compositions and materials, their manufacture and uses thereof have been iisclosed. It should be apparent, however, to those skilled in the art that many nore modifications besides those already described are possible without departing rom the inventive concepts herein. The inventive subject matter, therefore, is not to be restricted except in the spirit of the disclosure. Moreover, in interpreting the disclosure, all terms should be interpreted in the broadest possible manner consistent with the context, hi particular, the terms 'comprises" and "comprising" should be interpreted as referring to elements, components, or steps in a nonexclusive manner, indicating that the referenced elements., components, or teps
may he present, or utilized, or combined with other elements, components, or steps that are not expressly referenced.

We claim
1. A spun fiber having at least two different melting points, which comprises a composition
itself comprising:
a first fiber constituent having a first melting point;
a second fiber constituent having a second melting point, said second melting point
different than said first melting point;
one of said first and second fiber constituents present in said composition in an amount
greater than the other of said first and second fiber constituents; and
a gelling agent that solvates at least one of the first fiber constituent or the second fiber
constituent,
wherein the at least one gelling agent significantly reduces co-polymerization of the fiber
constituents in the composition, and the at least one gelling agent comprises less than SO
weight percent of the composition.
2. The spun fiber as claimed in claim 1, comprising at least one additional fiber constituent having a melting point that is different from the first melting point and the second melting point.
3. The spun fiber as claimed in claim 1, wherein at least one of the first fiber constituent and the second fiber constituent comprises at least one amide-based polymer.
4. The spun fiber as claimed in claim 3, wherein the at least one amide-based polymer comprises a nylon compound.
5. Thespun fiber as claimed in claim 4, wherein the nylon compound comprises nylon-6.
6. The spun fiber as claimed in claim 4, wherein the nylon compound comprises nylon-6,6.
7. The spun fiber as claimed in claim 4, wherein the nylon compound comprises a co¬polymer.

8. The spun fiber as claimed in claim 7, wherein the co-polymer comprises nylon-6,6,6.
9. The spun fiber as claimed in claim 1, wherein the at least one gelling agent comprises lactam.
10. The spun fiber as claimed in claim 9, wherein the lactam comprises caprolactam.
11. The spun fiber as claimed in claim 1, wherein the first fiber constituent comprises nylon 6,6,6, the second fiber constituent comprises nylon-6, and the gelling agent comprises a lactam-based compound.
12. The spun fiber as claimed in claim 1, wherein the at least one gelling agent comprises less than 40 weight percent of the composition.
13. The spun fiber as claimed in claim 1, wherein the at least one gelling agent comprises less than 30 weight percent of the composition.
14. The spun fiber as claimed in claim 1, wherein the at least one gelling agent comprises less than 20 weight percent of the composition.
15. The spun fiber as claimed in claim 1, wherein the at least one gelling agent comprises less than 10 weight percent of the composition.
16. The spun fiber as claimed in claim 1, wherein the at least one gelling agent comprises less than 5 weight percent of the composition.
17. The spun fiber as claimed in any of the preceding claims as and when used as a carpet product.
18. The spun fiber as claimed in claim 3, wherein each of the first fiber constituent and the second fiber constituent comprises at least one amide-based polymer.

19. A method of producing a spun fiber according to claim 1, comprising:
providing a first fiber constituent having a first melting point;
providing a second fiber constituent having a second melting point, wherein the first
melting point and the second melting point are dissimilar;
providing at least one gelling agent;
mixing the first fiber constituent, the second fiber constituent and the at least one gelling
agent to form a pre-fiber composition;
and spinning the pre-fiber composition into a fiber.
20. The method as claimed in claim 19, comprising providing at least one additional fiber
constituent having a melting point that is different from the first melting point and the
second melting point.
21. The method as claimed in claim 19, wherein at least one of the first fiber constituent and
the second fiber constituent comprises at least one amide-based polymer.
22. The method as claimed in claim 20, wherein the at least one amide-based polymer comprises a nylon compound.
23. The method as claimed in claim 22, wherein the nylon compound comprises nylon-6.
24. The method as claimed in claim 22, wherein the nylon compound comprises nylon 6,6.

Documents:

2852-DELNP-2006-Abstract-(06-07-2011).pdf

2852-delnp-2006-abstract.pdf

2852-DELNP-2006-Claims-(06-07-2011).pdf

2852-DELNP-2006-Claims-(07-05-2012).pdf

2852-delnp-2006-claims.pdf

2852-DELNP-2006-Correspodence Others-(08-07-2011).pdf

2852-delnp-2006-Correspondence Others-(06-07-2011).pdf

2852-DELNP-2006-Correspondence Others-(07-05-2012).pdf

2852-delnp-2006-correspondence-others-1.pdf

2852-delnp-2006-description(complete).pdf

2852-DELNP-2006-Drawings-(08-07-2011).pdf

2852-delnp-2006-drawings.pdf

2852-delnp-2006-Form-1-(06-07-2011).pdf

2852-delnp-2006-form-1.pdf

2852-delnp-2006-form-18.pdf

2852-delnp-2006-Form-2-(06-07-2011).pdf

2852-delnp-2006-form-2.pdf

2852-delnp-2006-Form-3-(06-07-2011).pdf

2852-DELNP-2006-Form-3-(07-05-2012).pdf

2852-delnp-2006-form-3.pdf

2852-delnp-2006-form-5.pdf

2852-delnp-2006-GPA-(06-07-2011).pdf

2852-delnp-2006-gpa.pdf

2852-delnp-2006-pct-311.pdf

2852-delnp-2006-pct-search report.pdf

2852-delnp-2006-Petition-137-(06-07-2011).pdf

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Patent Number

254178

Indian Patent Application Number

2852/DELNP/2006

PG Journal Number

40/2012

Publication Date

05-Oct-2012

Grant Date

27-Sep-2012

Date of Filing

19-May-2006

Name of Patentee

HONEYWELL INTERNATIONAL INC.,

Applicant Address

101 COLUMBIA ROAD, P.O.BOX 2245, MORRISTOWN, NEW JERSEY 07960, U.S.A.

Inventors:

#	Inventor's Name	Inventor's Address
1	JOHN B. BOYLE	305 REDBIRD DRIVE, CHESTER, CA 23836, USA;
2	SAMIR ABDALLA	1301 MEDICAL CENTER DRIVE APT. 522, CHULA VISTA, CA 91911, USA;
3	DALE A. HANGEY	629 GLENMEADOW ROAD, MIDLOTHIAN, VA 23113, USA
4	JAMES A. KWEEDER	2835 PINE MEADOW CIRCLE, CHESTER, VA 23831, USA,

PCT International Classification Number

C08K5/34; C08K5/3412; C08K5/00

PCT International Application Number

PCT/US2004/038185

PCT International Filing date

2004-11-15

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	10/717,048	2003-11-18	U.S.A.