巴西专利BR112012016568B1 bicomponent fiber composed of a polyethylene-based resin and a high melting point, non-woven resin,

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专利摘要:
BICOMPONENT FIBER. The present invention relates to a new bicomponent fiber, a non-woven fabric comprising the aforementioned new bicomponent fiber and sanitary products produced therefrom. The bicomponent fiber contains a polyethylene-based resin that forms at least part of the fiber surface longitudinally continuously and is characterized by a comonomer distribution constant greater than about 45, a recrystallization temperature between 85ºC and 110ºC, a tan value delta at 0.1 rd / s of about 15 to 50, and a complex viscosity at 0.1 rad / s of 1400 Pa.s or less. Nonwoven fabrics comprising the new two-component fiber, according to the present invention, are not only excellent in softness, but also have high strength, and can be produced in commercial volumes at lower costs due to higher yields and requiring less energy.
公开号:BR112012016568B1
申请号:R112012016568-2
申请日:2010-12-31
公开日:2021-01-26
发明作者:Jörg Dahringer；Bernd A. Blech；Werner Stefani；Werner Grasser；Mehmet Demirors；Gert Claasen
申请人:Trevira Gmbh；
IPC主号:

专利说明:

[0001] [001] The present invention relates to a new bicomponent fiber, a nonwoven comprising said bicomponent fiber and sanitary products produced with them. The non-woven fabrics comprising the new two-component fiber, according to the present invention, are not only excellent in softness, but also have high strength, and can be produced in commercial volumes at lower costs due to greater passages and which require less energy.
[0002] [002] Non-woven fabrics, such as non-woven fabrics spunbonded using non-woven fabrics produced using carding, meltblowing, or airlaid techniques have been used in a wide variety of applications in recent years, also for sanitary products produced from them.
[0003] [003] A polyethylene non-woven fabric, whose resin fibers are formed from polyethylene, is known for its softness and good tact (EPA-0.154,197). Polyethylene fibers are, however, difficult to swell and, therefore, difficult to allow to have a thinner denier that is necessary to obtain a good softness of a fabric. Non-woven formed of polyethylene fibers dissolve easily when subjected to a heat / pressure treatment with a calender cylinder, and what is even worse, it easily wraps around the cylinder due to the low resistance of the fibers. Measures have been taken against the above problems in which the treatment temperature is lowered; however, in such a case, thermal adhesion is capable of being insufficient, which leads to another problem of being unable to obtain nonwoven with sufficient strength and friction firmness in reality, polyethylene nonwoven is inferior in resistance to a non-woven polypropylene.
[0004] [004] To solve the problems mentioned above, techniques have been proposed for using a bicomponent fiber like a core coat using a polypropylene resin, polyester, etc., as a core and polyethylene as a coating (Japanese Patent Laid-Open n 2-182960 and Japanese Patent Laid-Open No. 5-263353).
[0005] [005] However, non-woven fabrics, which are formed of bicomponent fibers of the core coat type as described above, do not have as much softness or strength as are suitable for use as sanitary materials. Specifically, when the amount of polyethylene as a constituent of the coating is increased, the softness of the nonwoven is increased, but its strength is not allowed to be sufficient, and as a result it is likely to fracture during the process. On the other hand, when the constituent of the core is increased, the nonwoven is allowed to have sufficient strength, but it is poor in softness and its quality, as a material for sanitary goods, decreases. Thus, it was difficult to obtain a nonwoven having both of the above performances at a satisfactory level.
[0006] [006] Many of these bicomponents of the core coating type comprise a polyethylene coating with a polyester or polypropylene core. The responsible polyethylenes typically used in such applications have recrystallization temperatures that are generally greater than 110 ° C.
[0007] [007] A first solution to the problem mentioned above is described in EP-A-1,057,916 which describes spunbonded nonwoven fabrics for disposable sanitary products made from conjugated fibers. Such conjugated fibers having a high-melt core and a low-melt coating material can be of the wing-side type. The proposed low melting material is a polyethylene-based resin having a first high melting point in the range of 120 to 135 ° C and a second low melting point in the range of 90 to 125 ° C, the melting point of the second low melting material being at least 5 ° C below the first high melting point. Such low-fusion polyethylene resins are particularly complex to produce and cause problems during fiber spinning and in the subsequent use of such conjugated fibers in the production of non-woven fabrics, in particular non-woven fabrics produced using techniques of carding, melt-blowing or airlaid.
[0008] [008] However, it would still be desirable to lower the melting point of the polyethylene to allow a faster line speed due to the lower agglutination temperature and less energy use. On the other hand, the decrease in the melting point of polyethylene is associated with significant processing problems during fiber spinning. For expanded applicability for use in bonding fibers, such fibers must have the following characteristics: good spinning performance, so that smoke, fiber breaks and fiber bonding are minimized during the spinning process; fibers also need to have a low COF to allow the ability to be textured; good tensile properties of the fibers; ability to be promptly cut; ability to be processed in the airlaid process and ability to be bonded using the thermal bonding process in the air at the lowest temperature without the fibers becoming sticky. In addition, the outer layer of the bicomponent fiber must have good agglutination to the inner core (substrate) as well as to other fibrous products.
[0009] [009] Consequently, the objective of the present invention is to solve the problem mentioned above, in particular, to provide a bicomponent fiber that provides a non-woven fabric with excellent softness and feel as well as with sufficient strength and that can be produced in existing commercial equipment. lower costs.
[0010] [0010] The objective of the present invention is directed to a bicomponent fiber composed of a resin based on polyethylene (A) and a resin with a high melting point (B) whose melting point is higher than that of resin based on polyethylene (A) at least 10 ° C, the weight ratio of the polyethylene-based resin component (A) to the high melting point resin (B) being in the range 50/50 to 10/90, and the polyethylene-based resin (A) forming at least part of the fiber surface continuously longitudinally where the polyethylene-based resin (A) is characterized by a Comonomer Distribution Constant greater than about 45, a recrystallization temperature between 85 ° C and 110 ° C, a tan delta value at 0.1 rad / s of about 15 to 50, and a complex viscosity at 0.1 rad / s of 1400 Pa.s or less.
[0011] [0011] Other purposes of the present invention are nonwoven fabrics comprising bicomponent fibers as described above. Preferably such non-woven fabrics comprise the bicomponent fibers of the present invention as wavy textured fibers and / or flat non-textured fibers. In addition, such nonwoven comprises the bicomponent fibers previously referred to as cut fiber and / or continuous filament fiber.
[0012] [0012] The preferred non-woven fabrics are (i) non-woven wetlaid, (ii) non-woven air-laid and (iii) non-woven carded.
[0013] [0013] Another object of the present invention is a sanitary product comprising non-woven fabrics according to the present invention. Definitions
[0014] [0014] The term "composition" as used, includes a mixture of materials comprising the composition, as well as the products of the reaction and products of the decomposition formed from materials of the composition.
[0015] [0015] The terms "mixture" and "polymer mixture", as used, mean an intimate physical mixture (that is, without reaction) of two or more polymers. A mixture may or may not be miscible (phase not separated at the molecular level). A mixture may or may not be separate phases. A mixture may or may contain one or more domain configurations, as determined by electronic transmission spectroscopy, light scattering, x-ray scattering, and other methods known in the art. The mixing can be carried out by physically mixing the two or more polymers at the macro level (for example, resins or melt mix compounds) or at the micro level (for example, simultaneous shaping within the same reactor).
[0016] [0016] The term "long chain branched polymer" refers to polymers where the polymer backbone contains branches that are longer than the co-monomers typically used (for example, longer than 6 or 8 carbon atoms). A long chain branched polymer contains more than 0.2 long chain branches per 1000 carbon atoms.
[0017] [0017] The term "linear" refers to polymers where the polymer backbone lacks measurable or demonstrable long chain branches, for example, the polymer can be replaced with an average of less than 0.01 long chain per 1000 atoms of carbon.
[0018] [0018] The term "polymer" refers to a polymeric compound prepared by polymerizing monomers, whether they are of the same or different types. The generic term polymer therefore involves the term "homopolymer", generally used to define a polymer prepared from just one type of monomer, and the term "interpolymer" as defined.
[0019] [0019] The term "interpolymer" refers to polymers prepared by the polymerization of at least two different types of monomers. The generic term interpolymer includes copolymers, generally used to refer to polymers prepared from two different monomers, and polymers prepared from more than two different types of monomers,
[0020] [0020] The term "ethylene-based polymer" refers to a polymer that contains more than 50 mole percent ethylene monomer polymerized (based on the total amount of polymerization monomers) and, optionally, can contain at least one comonomer. Two-component fiber
[0021] [0021] The bicomponent fiber of the present invention can be of any shape and is not limited to a particular shape. However, bicomponent fibers of the core coating type and bicomponent fibers of the side-to-side type are preferred. Resin (A) based on polyethylene
[0022] [0022] The bicomponent fiber of the present invention contains a polyethylene-based resin (A) which has a Comonomer Distribution Constant greater than about 45; a recrystallization temperature between 85 ° C and 110 ° C, a delta tan value at 0.1 rad / s of 1400 Pa.s or less.
[0023] [0023] Ethylene-based polymer resin compositions can also be characterized as having a single differential scanning calorimetry (DSC) melting peak within the temperature range of 85 ° C to 110 ° C.
[0024] [0024] Ethylene-based polymer resin compositions can also be characterized as having a Comonomer Distribution Constant greater than about 45, more preferably greater than 50, more preferably greater than 55 and of the order of 400, more preferably of order of 100. In particular, the ethylene-based polymer resin compositions have a Comonomer distribution composition in the range of 45 to 400, more preferably in the range of 50 to 100, and most preferably still in the range of 55 to 100.
[0025] [0025] Ethylene-based polymer compositions are those made in high pressure reactors using the free radical polymerization process, preferably using a peroxide-based free radical initiator. The preferred polyethylene resin has a melting index (measured according to ASTM D 1238m Condition 190 ° C / 2.16 kg) in the range of 5 to 25 g / 10 min, more preferably 5 to 20.
[0026] [0026] Preferred ethylene resins have a density in the range of 0.910 to 0.930 g / cm3, more preferably 0.915 to 0.925 g / cm3.
[0027] [0027] Ethylene-based polymer compositions can also be characterized by having a recrystallization temperature peak in the range of 85 ° C to 110 ° C, preferably from 90 to 105 ° C.
[0028] [0028] Ethylene-based polymer compositions can also be characterized by having more than about 0.2 long chain branches / 1000 carbon atoms, preferably from about 0.2 to about 3 long chain branches / 1000 carbon atoms.
[0029] [0029] Ethylene-based polymer compositions can also be characterized by having a complex viscosity at 0.1 rad / s of 1400 Pa.s or less, and preferably at 100 rad / s of 500 Pa.s or less. More preferably, the resins of the present invention will have a complex viscosity at 0.1 rad / s in the range of 500 to 1200 and at 100 rad / s in the range of 150 to 450 Pa.s.
[0030] Preferred ethylene-based polymer compositions can also be characterized by having a tan delta value at 0.1 rad / s of about 15 to 50, preferably 15 to 40.
[0031] [0031] In some processes for the production of polyethylene-based resin (A), processing aids, such as plasticizers, can also be included in the ethylene-based polymer of the present invention. Such auxiliaries include, but are not limited to, phthalates, such as dioctyl phthalate and diisobutyl phthalate, natural oils such as lanolin, and paraffin, naphthalenic and aromatic oils obtained from petroleum refining, and liquid pitch resins or petroleum raw materials. Examples of classes of oils useful as processing aids include white mineral oils such as KAYDOL oil (Chemtura Corp .; Middlebury, Conn.) And SHELFLEX 371 naphthalene oil (Shell Lubricants; Houston, Tex.). Another suitable oil is TUFFLO oil (Lyondell Lubricants; Huston, Tex.).
[0032] [0032] In some processes, ethylene polymers are treated with one or more stabilizers, for example, antioxidants such as IRGANOX 1010 and IRGAFOS 168 (Ciba Specialty Chemicals; Glattbrug, Switzerland).
[0033] [0033] In general, polymers are treated with one or more stabilizers before extrusion or other melting processes. In other process configurations, other polymeric additives include, but are not limited to, ultraviolet light absorbers, antistatic agents, pigments, dyes, nucleating agents, fillers, glidants, fire retardants, plasticizers, processing aids, lubricants , stabilizers, smoke inhibitors, viscosity control agents, surface modifying agents and anti-blocking agents. The composition of the ethylene polymer can, for example, comprise less than 10 weight percent, combined of one or more additives, based on the weight of the ethylene polymers of the modality.
[0034] [0034] The ethylene polymer produced can also be composed. In some ethylene polymer compositions, one or more antioxidants may also be composed in the polymer and the polymer compound pelletized. The ethylene polymer compound can contain any amount of one or more antioxidants. For example, the ethylene polymer compound may comprise from about 200 to about 600 parts of one or more phenolic antioxidants to one million parts of the polymer. In addition, the ethylene compound polymer may comprise from about 800 to about 1200 parts of phosphite-based antioxidant for one million parts of the polymer.
[0035] [0035] Polyethylene-based resin (A) can be made using two or more reactors, one of which is a mixed return reactor with at least one reaction zone and a second reaction zone which is a laminar flow with at least two reaction zones. The product can also be advantageously made in a typical high pressure tubular process with two or more reaction zones with ethylene pressure at the entrance of the range from 180 MPa to 350 MPa (1800 bar to 3500 bar). The temperature at the entrance of the first reaction zone can advantageously be in the range of 200 MPa to 300 MPa (2000 to 3000 bar). The start of the polymerization temperature can be from 110 ° C to 150 ° C with the peak temperature from 280 ° C to 330 ° C. For the start of the reaction, the peroxide mixture was used to achieve the desired reaction rate at a given temperature and pressure as is known in the art. The exact composition of the free radical peroxide initiator mixture can be determined based on the details of the installations, process pressures, temperatures and residence times by those skilled in the art. For the production of the compositions of the present invention, a mixture of tertiary butyl peroctoate and dithercary butyl peroxide can advantageously be used in the first zone of the reactor at a ratio of the order of 14 to 3 based on volume. The same two peroxides can also be used in the second reaction zone at a volume ratio of 1 to 1. The exact quantities will depend on the purity of the reactors, the characteristics of the reactor and other process parameters and can be determined by each specific configuration by those skilled in the art.
[0036] [0036] The restart temperature of the second zone can be about 160 ° C to 230 ° C with a peak temperature of about 280 ° C to 330 ° C. A mixture of methyl ethyl ketone and propylene can be used as a chain transfer agent to control molecular weight. Typical ranges can be from about 10 to 5000 ppm by volume of methyl ethyl ketone and from about 0.1% by volume to 5% by volume of propylene depending on the desired complex viscosity ranges. Then, the polymer was separated from the process solvents and unreacted ethylene, pelleted through an extrusion machine and used without further processing.
[0037] [0037] Additives and auxiliaries can also be added to the postformation of ethylene polymer. Suitable additives include fibers, such as organic or inorganic particles, including clays, talc, titanium dioxide, zeolites, pulverized metals, in particular based on silver and / or silver ions, super absorbent materials, organic or inorganic fibers, including carbon fibers, silicon nitride fibers, steel wire or mesh, nylon or polyester string, nano-sized particles, clays, etc .; tackifiers, oil extenders including paraffinic or naphthalenic oils; and other natural and synthetic polymers, including other polymers that are made or can be made according to the methods of the modality. Resin (B) - high melting point resin
[0038] [0038] The bicomponent fiber of the present invention contains a high melting point resin (B), which typically forms the core portion of the bicomponent fiber of the core shear type according to the present invention. Such a high melting point resin (B) is a thermoplastic resin having a higher melting point than that of the polyethylene based resin (A) above, at least 10 ° C, preferably at least 20 ° C, more preferably at least 30 ° C.
[0039] Preferred high melting point (B) resins include polyolefin resins such as polypropylene-based polymers, polyester resins such as polyethylene terephthalate (PET) and polyamide resins such as nylon. Among all the resins above, polyester resins such as polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polyphthalene terephthalate (PEN) are most preferred.
[0040] Among the aforementioned propylene-based polymers, homopolymer propylene or copolymers of propylene and alpha olefins, such as ethylene, 1-butene, 1-hexene, 4-methyl-1-pentene and 1-octene are more preferred. Among all of the above copolymers, propylene-ethylene random copolymers comprised of propylene and a small amount of ethylene whose structural unit content of ethylene is 0.1 to 5 moles% are particularly preferable. The use of such a copolymer provides good spinning capacity and productivity of its bicomponent fibers and a nonwoven having good softness. The term "good spinning capacity" used here means that neither yarn breakage nor filament melting occurs during extrusion by the spinning nozzles and during extraction.
[0041] [0041] Preferably the aforementioned propylene-based polymers have a melt flow rate (MFR; measured at 230 ° C and a load of 2.16 kg according to ASTM D1238) in the range of 20 to 100 g / 10 min in terms of obtaining a particularly excellent fiber in balancing the spinning capacity and strength of the fiber.
[0042] [0042] Preferably the molecular weight distribution (Mw / Mn) of the aforementioned propylene-based polymers, when measured by gel permeation chromatography (GPC), is in the range of 2.0 to 4.0, and more preferably mW / Mn is in the range of 2.0 to 3.0 in terms of obtaining a two-component fiber good in spinning capacity and particularly excellent in fiber strength.
[0043] [0043] The core component may preferably consist of conventional melt-spinnable polyester material. All known types suitable for fiber production can, in principle, be considered as polyester material. Such polyesters essentially consist of components that are derived from aromatic dicarbonic acids and aliphatic diols. Commonly used, aromatic dicarbonic acid components are the divalent residues of benzyl dicarbonic acids, particularly terephthalate acid and isophthalic acid; commonly used diols have 3 to 4 C atoms, ethylene glycol being particularly suitable.
[0044] [0044] Of particular advantage is a polyester material of which at least 85 moles% consists of polyethylene terephthalate. The remaining 15 moles% are then composed of dicarbonic acid units and glycol units that act as so-called modifiers and that allow the expert to also influence the physical and chemical properties of the fibers produced in a specific way. Examples of such dicarbonic acid units are residues of isophthalic acid or aliphatic dicarbonic acid, for example, glutaric acid, adipinic acid, sabbatic acid, examples of diol residues, with a modifying action are those of longer chain diols, for example for example, propane diol or butane diol, or di- or tri-ethylene glycol, or, if available in a small amount, polyglycol with a molecular weight of 500 to 2000 g / mol.
[0045] [0045] Polyesters containing at least 95 mole% polyethylene terephthalate, particularly those of unmodified polyethylene terephthalate, are particularly preferable. Such polyesters normally have a molecular weight equivalent to an intrinsic (IV) viscosity of 0.5 to 1.4 (dl / g), measured in solutions of dichloroacetic acid at 25 ° C. Additions
[0046] [0046] The polyethylene-based resin (A) that forms the fiber coating portion and / or the high melting point resin (B) that forms the core portion the same, can be mixed with additives, such as material coloring, thermosetting stabilizer, lubricant, nucleating agent, and other polymers according to the situation.
[0047] [0047] The coloring materials applicable to the present invention include, for example, inorganic coloring materials, such as titanium oxide and calcium carbonate, and organic coloring materials, such as phthalocyanine.
[0048] [0048] Thermoresistant stabilizers include, for example, phenol-based stabilizers such as BHT (2,6-di-t-butyl-4-methylphenol).
[0049] [0049] Lubricants include, for example, oleic starch, erucic starch, and stearic starch. In the present invention, particularly preferably 0.1 to 0.5% by weight of lubricant is mixed with the polyethylene-based resin (A) that forms the coating portion, since the bicomponent fiber, obtained in the above manner , may have an increased friction firmness.
[0050] [0050] Another group of additives are adhesion promoters that promote adhesion between the polyethylene-based resin (A) that forms the fiber coating portion and the high melting resin (B). Suitable adhesion promoters are maleic acids (MSA), or maleic acid anhydride (MAH) that promote such adhesion. Typical amounts added are 0.05 to 3% by weight. Most preferably the adhesion promoter is added to the polyethylene (A) -based resin in the melt during the spinning of the bicomponent fiber (Please check the quantity and potential of other additives to be said).
[0051] [0051] Preferably the weight ratio of the polyethylene-based resin component (A) to the high melting point resin (B) is in the range of 50/50 to 10/90, and in terms of obtaining a fiber excellent in balance of softness and firmness of friction, preferably in the range of 50/50 to 20/80 and more preferably in the range of 40/60 to 30/70.
[0052] [0052] When the proportion of polyethylene-based resin (A) to the bicomponent fiber exceeds 50, there may be some parts that have not been improved in fiber strength. On the other hand, when the proportion of polyethylene-based resin (A) to a bicomponent fiber is low, on the order of less than 10, some parts may be poor in both softness and touch in the fabric obtained.
[0053] [0053] The area ratio of the coating portion to the core portion in a cross-section of the core-coating type bicomponent fiber according to the present invention is generally almost the same as the weight component ratio described above, and is in the range 50/50 to 10/9, preferably in the range 50/50 to 20/80, and more preferably in the range 40/60 to 3070.
[0054] [0054] The bicomponent fiber of the core-coating type according to the present invention can be a concentric-type fiber, where the circular core portion and the ring-shaped covering portion have the same center and the same cross section in the fiber, the core portion being surrounded by the coating portion, or of an eccentric type, where the centers of the core portion and the coating portion are different from each other. In addition, the bicomponent fiber of the core-coating type may be an eccentric type where the core portion is partially exposed on the surface of the fiber.
[0055] [0055] For bicomponent fibers of the core-coating type, their fineness is preferably from 0.7 to 20 dtex and, in terms of obtaining a fiber more excellent in softness, more preferably from 0.9 to 15 dtex. Two-component fiber production
[0056] [0056] Apparatus of the prior art, with suitable nozzles, can be used to produce bicomponent fibers according to the present invention.
[0057] [0057] In addition to the common two-component core-coating fibers, with a core / coating profile where the core occupies an eccentric position are also part of this invention. These so-called eccentric bicomponent fibers are described in greater detail in US 2005/0093197 which forms part of that specification in relation to such an eccentric bicomponent design.
[0058] [0058] The spinning speed to form the bicomponent fiber according to the present invention is typically between 600 and 2000, preferably between 800 and 1500 m / min.
[0059] [0059] The escape speed on the escape surface of the nozzle is compared to the spinning speed and the exit ratio so that the fiber finally produced has a circulation of 0.7 to 20 dtex, preferably from 0.9 to 15 dtex .
[0060] [0060] The raw materials used for the production of the bicomponent fiber, according to the present invention, are melted independently in the extrusion machine, etc., and each melt is extruded through a spinner with bicomponent fiber spinning nozzles constructed to extrude the melt in order to form the desired structure, for example, core-coating, so that the bicomponent fiber is expanded.
[0061] [0061] The dilated bicomponent fiber is then cooled with a refrigerant fluid, allowed to receive a traction force by air stretching to have a predetermined fineness as defined above. In order to produce spunbonded nonwoven fabrics, the newly spinned bicomponent fiber according to the present invention is collected on a collecting belt to deposit to a predetermined thickness, so that the spunbonded nonwoven of the bicomponent fiber can be obtained. Spunbonded bicomponent fiber nonwoven can also be consolidated, for example, by subjecting the nonwoven to another wrapping, for example, by the modeling process using a shaping cylinder by the known methods of needling / hydro wrapping.
[0062] [0062] In order to produce other non-woven fabrics, such as wet-laid non-woven fabrics, air-laid non-woven fabrics and carded non-woven fabrics, other treatments of recently spinning bicomponent fiber are required. Two-component fiber treatment after spinning
[0063] [0063] To produce nonwoven, such as wet-laid nonwoven, air-laid nonwoven fabrics and carded nonwoven fabrics, other treatments are required after spinning.
[0064] [0064] The bicomponent fibers according to the present invention are typically stretched with individually different ratios between 1.2 and 4.0, the stretch ratio ranging from approx. 0.1, that is, they are 1.2, 1.3, 1.4 ... up to 4.0. The resulting total stretch ratio is between 1.2 and 4.0.
[0065] [0065] The stretching of the bicomponent fiber occurs at the same temperature or at different temperatures between 40 and 70 ° C, preferably at 55 ° C.
[0066] [0066] Subsequently, the stretched bicomponent fiber can be corrugated, typically in a stuffer box.
[0067] [0067] After waving in the stuffer box, the bicomponent fibers are subjected to heat treatment at up to 100 ° C, with a retention time of 3 to 20 minutes, more preferably 12 to 15 minutes.
[0068] [0068] The degree of stretching can be improved using eccentric bicomponent fibers as described above.
[0069] [0069] Typically the degree of stretching can be expressed as stretching contraction (K1) which is calculated using the equation:
[0070] [0070] K1 = (length of hand drawn - length drawn) / length not drawn (standard climate, 20 ° C +/- 2 ° C, relative humidity: 60 - 65%).
[0071] [0071] The number of undulations is typically given in undulations / cm.
[0072] [0072] Two-component fibers, whether textured or not, can be cut into cut fibers, and then processed into suitable products. The lengths of the typical cut fiber are 0.2 to 15 cm, preferably 0.2 to 8 cm, more preferably 0.3 to 6 cm.
[0073] [0073] For use in wet-laid non-woven fabrics, the bicomponent fiber according to the present invention is typically a non-textured flat fiber that is not textured after spinning. Preferably such flat fibers have a length of 0.2 cm to 3 cm, more preferably 0.3 cm to 2.5 cm.
[0074] [0074] For use in air-laid non-woven fabrics the bicomponent fiber according to the present invention is typically a textured fiber. Preferably, the stretch contraction (K1) is 3 to 7% d The number of undulations is 3 to 6 undulations / cm.
[0075] [0075] For this in carded non-woven fabrics, the bicomponent fiber according to the present invention is typically a textured fiber. Preferably the stretch contraction (K1) is 8 to 15% and the number of undulations is 5 to 8 undulations / cm.
[0076] [0076] Subsequently, bicomponent fibers can be processed into suitable products, in particular into textile products, preferably hygienic products, hygienic textile fabrics. Non-woven hygienic fabrics, diapers, towels or linings and the like, but also in cotton swabs, etc.
[0077] [0077] As a result of choosing an eccentric coating core design, such bicomponent fibers are given an additional ripple which, during further processing, can be started by heat treatment at temperatures exceeding approx. 100 ° C. Two-component fiber non-woven
[0078] [0078] Other purposes of the present invention are nonwoven fabrics comprising bicomponent fibers as described above.
[0079] [0079] Due to the nature of the polyethylene-based resin (A) which forms at least part of the fiber surface continuously longitudinally where the polyethylene-based resin (A) is characterized by a comonomer distribution constant greater than about 45, a recrystallization temperature between 85 ° C and 110 ° C, a tan delta value at 0.1 rad / s of about 15 to 50, and a complex viscosity at 0.1 rad / s of 1400 Pa.s or less, the processing of nonwoven fabrics can be significantly improved.
[0080] [0080] The specific polyethylene-based resin (A) allows processing of temperature when the nonwoven is formed and thereafter thermal bonding. Due to the lower melting point of the polyethylene-based resin (A) which is below 120 ° C, a lower bonding temperature and less energy use is required. In addition, higher line speeds are possible resulting in lower production costs. Despite the lower melting point, no significant processing problems occur during fiber spinning. These and other advantages occur, for example, when the bicomponent fiber according to the present invention PE is used in non-woven fabrics combined with cellulose-based fibers, which are extremely sensitive to heat. Even a small reduction in the thermal bonding processing temperature can have a significant commercial advantage due to the high volumes. In addition, the potential fire risk is also reduced. In addition, the potential thermal damage of other materials mixed with the bicomponent fiber according to the present invention can be reduced or even avoided.
[0081] [0081] Preferred non-woven fabrics are (i) wet-laid non-woven fabrics, (ii) air-laid non-woven fabrics and (iii) carded non-woven fabrics.
[0082] [0082] Non-woven fabrics according to the present invention can be mixed with other fibrous materials.
[0083] [0083] Preferably, non-woven fabrics according to the present invention at a basis weight of 10 to 500 g / m2. The base weight stated above depends on the end use.
[0084] [0084] Preferably, the non-woven fabrics according to the present invention comprise two-component fibers textured or not and cut into cut fibers, preferably having a length of cut fiber from 0.2 cm to 15 cm, more preferably 0.2 cm to 8 cm , and even more preferably 0.3 to 6 cm.
[0085] [0085] Preferably, the nonwoven according to the present invention is a wet-laid nonwoven typically comprising the bicomponent fiber according to the present invention, said bicomponent fiber being a non-textured pana fiber, preferably having a length of 0, 2 cm to 3 cm, more preferably 0.3 cm to 2.5 cm.
[0086] [0086] Preferably the nonwoven according to the present invention is an air-laid nonwoven typically comprising the bicomponent fiber according to the present invention, said bicomponent fiber being textured, preferably having a stretch contraction (K1) of 3 to 7 % and the number of dimples of 3 to 6 dimples / cm, preferably having a length of 0.2 cm to 3 cm, more preferably of 03 cm to 2.5 cm.
[0087] [0087] Preferably the nonwoven according to the present invention is a carded nonwoven typically comprising the bicomponent fiber according to the present invention, said bicomponent fiber being textured, preferably having a stretch contraction (K1) of 8 to 15% and the number of corrugations from 5 to 8 corrugations / cm, preferably having a length of 2 cm to 15 cm, more preferably 3 cm to 8 cm.
[0088] [0088] In addition, the nonwoven according to the present invention can be a spunbonded nonwoven comprising continuous filaments or non-continuous fibers, both of the bicomponent type composed of polyethylene-based resin (A) and high-point resin melting points (B) mentioned above.
[0089] [0089] The formation of the nonwoven according to the present invention can be done using the existing techniques.
[0090] [0090] The non-woven fabrics according to the present invention can be mixed with other fibrous materials and / or particulate materials, depending on the intended use.
[0091] [0091] For industrial applications, non-woven fabrics according to the present invention comprise other fibrous materials such as organic and / or inorganic fibrous materials, which can also be recyclable materials.
[0092] [0092] The term organic fibrous materials includes, in addition to organic polymer resins, also natural fibrous materials. Within organic polymer resins, all reliable cast materials can be used. Particular preference is given to reliable fused organic polymers such as polyolefins, for example, polyethylene and / or polypropylene, polyesters, for example, polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polyphthalene terephthalate (PEN), terephthalate polytrimethylene (PTT), polyamides, for example, nylon.
[0093] [0093] For industrial applications, non-woven fabrics according to the present invention comprise particulate materials, such as particulate inorganic materials, in particular milling materials.
[0094] [0094] The term inorganic fibrous materials includes - in addition to others - those based on glass and / or minerals, in particular recycled materials.
[0095] [0095] Industrial applications include filter media and battery separators.
[0096] [0096] For textile applications, preferably hygiene and / or sanitary products, the non-woven fabric according to the present invention comprises other fibrous materials. Preferred fibrous materials are pulp, cellulose, cotton, homo- and copolymers based on polyethylene or polypropylene, in particular based on recycled materials.
[0097] [0097] Subsequently, non-woven fabrics according to the present invention can be processed into suitable products or processed to form an integral part of these products, in particular textile products, preferably hygiene products, textile hygiene fabrics, non-woven hygiene fabrics , disposable diapers, absorbents, diapers, towels or liners and the like, but also cotton swabs, etc.
[0098] [0098] For some textile applications, nonwoven fabrics according to the present invention in addition to other fibrous materials can comprise particulate materials, such as super absorbent materials, inter alia used in disposable diapers.
[0099] [0099] Nonwoven fabrics according to the present invention can be combined with other covering materials or layers of covering to provide an even softer touch. A suitable covering or layer of covering are melt-blown non-woven fabrics formed from fibers having a diameter of 1 to 10 µm. Testing methods Density:
[0100] [00100] Samples that are measured for density are prepared according to ASTM D 1928. Measurements are made within one hour of pressing the sample using method B of ASTM D792. Fusion index
[0101] [00101] The melting index, or I2, is measured according to ASTM D 1238, condition 190 ° C / 2.16 kg, and is reported in grams eluted for 10 minutes. I10 is measured according to ASTM D 1238, condition 190 ° C / 10 kg, and is reported in grams eluted for 10 minutes. DSC Crystallinity
[0102] [00102] Differential scanning calorimetry (DSC) can be used to measure the melting and crystallization behavior of a polymer over a wide temperature range. For example, TA Q1000 DSC instruments, equipped with an RCS (refrigerated cooling system) and an auto-sampler are used to perform this analysis. During the tests, a flow of purifying nitrogen gas of 50 ml / min is used. Each example is melted pressed into a thin film at about 175 ° C, the melted sample is then cooled in air to room temperature (~ 25 ° C). A specimen of 3 to 10 mg and 6 mm in diameter is extracted from the cooled, weighed polymer, placed in a light aluminum pan (ca 50 mg), and corrugated. The analysis is then performed to determine its thermal properties. The thermal behavior of the sample is determined by increasing and decreasing the temperature of the samples to create a heat flow versus a temperature profile. Initially, the sample is heated quickly to 180 ° C and kept isothermal for 3 minutes to remove its thermal history. The sample is then cooled to –40 ° C at a cooling rate of 10 ° C / min and kept isothermal for a - 40 ° C for 3 minutes. The sample is then heated to 150 ° C (this is the "second heating ramp") at a heating rate of 10 ° C / min. The cooling and second heating curves are recorded. The cooling curve is analyzed by adjusting the end points of the baseline to -20 ° C. The heating curve is analyzed by adjusting the end points of the baseline of -20 ° C until the end of the melt. The values determined are peak melting temperature (Tm), peak recrystallization temperature (Tp), heat of melting (Hf) (in Joules per gram), and the percent crystallinity calculated for polyethylene samples using equation 2 : % crystallinity = ((Hf) / (292 J / g) x 10 (Eq. 2)
[0103] [00103] The melting heat (Hf) and the melting peak temperature are reported from the second heating curve. The peak recrystallization temperature is determined from the cooling curve as Tp. Frequency scanning by dynamic mechanical spectroscopy (DMS)
[0104] [00104] The fusion rheology, the frequency sweep at constant temperature, were performed using a TA Instruments ARES rheometer equipped with 25 mm parallel plates under a purifying nitrogen gas. Frequency scans were performed at 190 ° C for all samples at a span of 2.0 mm and at a constant tension of 10%. The frequency range is from 0.1 to 100 rad / s. The stress response was analyzed in terms of amplitude and phase, from which the storage modules (G '), the loss module (G "), and the melt dynamic viscosity (ŋ *) were calculated. CEF Method
[0105] [00105] The comonomer distribution analysis is performed with fractionation of the crystallization elution (CEF) (PolymerChar in Spain) (B. Monrabal et al., Symp. 257, 71-79 (2007)). Ortho-dichlorobenzene (ODCB) with 600 ppm of antioxidant butylated hydroxytoluene (BHT) is used as a solvent. Sample preparation is done with a self-sampler at 160 ° C for 2 hours under agitation at 4 mg / ml (unless otherwise specified. The injection volume is 300 µl.
[0106] [00106] The CEF temperature profile is: crystallization at 3 ° C / min from 110 ° C to 30 ° C, thermal equilibrium at 30 ° C for 5 minutes, elution at 3 ° C / min from 30 ° C to 140 ° Ç. The flow rate during crystallization is 0.052 ml / min. The flow rate during elution is 0.50 ml / min. The data is collected at a data point / second.
[0107] [00107] The CEF column is compressed by the Dow Chemical Company with 125 µm ± 6% glass beads (MO-SCI Specialty Products) with 3.175 mm (1/8 inch) stainless tubing. The glass beads are acid-washed by MO-SCI Specialty at the request of the Dow Chemical Company. The column volume is 206 ml. The column temperature calibration is performed using a mixture of polyethylene NIST Standard Linear Reference Material 1475a (1.0 mg / ml) and Elcosane (2 mg / ml) in ODCB. The temperature is calibrated by adjusting the elution heating rate so that the linear polyethylene NIST 1475a has a peak temperature at 101.0 ° C, and Ecosane has a peak temperature at 30.0 ° C. The resolution of the CEF column is calculated with a mixture of linear polyethylene NIST 1475a (1.0 mg / ml) and hexacontane (Fluka, purum, ≥97.0%, 1 mg / ml). Baseline separation of NIST 1475a hexacontane and polyethylene is achieved. The hexacontane area (from 35.0 to 67.0 ° C) for the NIST 1475a area from 67.0 to 110.0 ° C is 50 to 50, the amount of soluble fraction below 35 ° C is < 1.8% by weight. The resolution of the CEF column is defined as: Resolution = peak temperature of NIST 1475a - peak temperature of hexacontane / half height width of NIST 1475a + half height width of hexacontane
[0108] [00108] The column resolution is 6.0%. CDC Method
[0109] [00109] The comonomer distribution constant (CDC) is calculated from the comonomer distribution profile by CEF, the CDC is defined as the comonomer distribution index divided by the comonomer distribution form factor multiplied by 100 (Equation 1 ).
[0110] [00110] The comonomer distribution index represents the fraction of the total weight of the polymer chain with the comonomer content ranging from 0.5 of the average comonomer content (average C) and 1.5 of the average C of 35.0 ° C at 119.0 ° C.
[0111] [00111] The comonomer distribution form factor is defined as the ratio of the half width of the comonomer distribution profile divided by the standard deviation of the comonomer distribution profile from the peak temperature (Tp).
[0112] [00112] The CDC is calculated according to the following steps:
[0113] [00113] Obtain the weight fraction at each temperature (T) (wT (T)) from 35 ° C to 119 ° C with a temperature step of 0,200 ° C with from the CEF according to equation 2.
[0114] [00114] Calculate the average temperature (Average) to the cumulative fraction of 0.500 (equation 3)
[0115] [00115] Calculate the corresponding average comonomer content in mole% (Average) at the average temperature (Average) by using the comonomer content calibration curve (equation 4). (3i). The comonomer content calibration curve is constructed using a series of reference materials with known amounts of comonomer content. Eleven reference materials with narrow comonomer distribution (mono-modal comonomer distribution in the CEF from 35.0 to 119.0 ° C) with an average weight of 35,000 to 115,000 mW (by conventional GPC) at a comonomer content ranging from 0, The mole% to 7.0 mole% are analyzed with CEF under the same experimental conditions specified in the experimental sections of CEF.
[0116] [00116] The comonomer distribution index is the fraction of the total weight with a comonomer content ranging from 0.5 ° Average to 1.5 ° Average. If average is greater than 98.0 ° C, the comonomer distribution index is set to 0.95.
[0117] [00117] The maximum peak height is obtained from the comonomer distribution profile looking for each data point for the highest peak from 35.0 ° C to 119 ° C (if two peaks are identical, then the lowest temperature is selected). Half width is defined as the temperature difference between the front temperature and the rear temperature at half the height of the maximum peak. The front temperature in the middle of the maximum peak is reached forward from 35 ° C, while the rear temperature in the middle of the maximum peak height is reached backwards from 119 ° C. In the case of a well-defined bimodal distribution where the difference in peak temperatures is equal to or greater than 1.1 times the sum of the half width of each peak, the half width of the polymer is calculated as the arithmetic mean of the half width of each peak.
[0118] [00118] The standard deviation of temperature (Stdev) is calculated according to equation 5.
[0119] [00119] An example of a comonomer distribution profile is shown in figure 1.
[0120] [00120] Schematic drawings for obtaining peak temperature, half width and average temperature from the CEF. Complex viscosity (use of dynamic melt viscosity) also known as Eta:
[0121] [00121] The dynamic viscosity of the melt was calculated from DMS measurements between 0.1 rad / s to 100 rad / s as outlined in the section on the DMS. Tan Delta
[0122] [00122] The tan delta was calculated from G 'and G "as follows: Tan δ = G "/ G" EXAMPLES
[0123] [00123] The present invention will be described in greater detail in relation to the examples and comparative examples shown below.
[0124] [00124] In general for this order, a series of performance attributes are required. First, the resin must be able to form a fiber in the molten state at economically viable rates.
[0125] [00125] Second, the resin must be good enough to form a good bond in the core fiber.
[0126] [00126] Third, the resin must have a melting point low enough for a good airlaid process as well as for thermal agglutination in the air to other substrates such as cellulose.
[0127] [00127] If the Tp is too high, the airlaid process is compromised, and the adhesion properties in the air are poor. If Tp is too low, then fiber adhesion becomes a problem. In fact, a relatively narrow melting range is ideal.
[0128] [00128] The example of the invention in Table 1 is made with the following specific parameters of the reaction:
[0129] [00129] In a free radical high pressure polymerization reactor in zone two, all ethylene is fed in the first zone at a pressure of 247 MPa (2470 bar). A mixture of 14.1% tertiary butyl peroxioctoate (by weight) and 2.8% dithercary butyl peroxide (by weight) is fed into the reactor's first reaction zone in an inert solvent typically used for such mixtures. The initiation temperature of the first zone is 136 ° C and the peak temperature of the first zone is 310 ° C. Also added to the first zone of the reactor is a mixture of methyl ethyl ketone of 1280 ppm by volume and 2.1% by volume of propylene in an inert solvent. To the second reaction zone is added a mixture of 7% (by volume) of tertiary butyl peroxioctoate and 7% (by volume) of butyl peroxide, dissolved in an inert solvent. No chain transfer additions are made to the second reaction zone. The internal temperature of the second reaction zone is 194 ° C and the peak temperature for the second reaction zone is 317 ° C. The total ethylene conversion at the reactor outlet is 28.7% based on the total ethylene feed at the beginning of reaction zone 1. The polymer is then devolatilized to remove unreacted ethylene, inert solvents and other impurities, and then it is pelleted. The pellets are used in the state, without further modifications.
[0130] [00130] This material forms the polyethylene-based resin (A) used in bicomponent firms according to the present invention. Since such resin (A) is more important, the properties have been investigated in the form of fibers made only from that resin (A).
[0131] [00131] Comparative example 1 is a low density polyethylene resin commercially available from Dow Chemical Company as LDPE PT7009.
[0132] [00132] Comparative example 2 is a high density polyethylene resin based on Ziegler Natta (HDPE) commercially available as ASPUN® 6934 resin, also from Dow Chemical Company.
[0133] [00133] Comparative example 3 is a linear low density polyethylene resin Ziegler Natta (LLDPE) commercially available from Dow Chemical Company as DOWFLEX® 2045 resin.
[0134] [00134] Comparative example 4 is a low density ultra low density polyethylene resin Ziegler Natta (ULLDPE) commercially available from Dow Chemical Company as ATTANE® 4606 resin.
[0135] [00135] It was discovered that only comparative examples 1, 2 and the example of the invention could be satisfactorily made into fibers. While comparative example 2 was good at forming fibers due to its high recrystallization temperature, it did not bind well to fibers at the desired low temperatures. A proper connection of this comparative example can only be made at high temperatures.
[0136] [00136] Comparative examples 3 and 4 were not suitable for fiber formation since their values eta 0.1 and eta 100 were very high for the formation of economical fibers at high speed.
[0137] [00137] Although example 1 is satisfactory in terms of fiber formation, in the airlaid process as well as in agglutination to heated air, it was inferior to the example of the invention in texturing. It was observed that it did not agglutinate well with the substrate fiber. It has surprisingly been found that good bonding to the substrate fiber requires that the ratio of G "and G '(tan delta) must be in a certain range. If tan delta is very low, then the coating resin is very elastic and does not provide good agglutination, as in the case of comparative example 1. If tan delta is very high, then the coating resin is not sufficiently elastic to make a good agglutination to the substrate fiber. Without good agglutination between the coating resin and the substrate fiber, no texturing adequate is obtained.
[0138] [00138] Additionally, we found that if the resin has a CDC value less than 45, the adhesion of the fires occurs at a given recrystallization peak temperature.

权利要求:
Claims (39)
[0001]
Two-component fiber composed of a polyethylene-based resin (A) and a high melting point resin (B) whose melting point is greater than that of polyethylene-based resin (A) by at least 10 ° C, the ratio by weight of the component of the polyethylene-based resin (A) for the high melting point resin (B) being in the range of 50/50 to 10/90, and the polyethylene-based resin (A) forming at least part of the fiber surface longitudinally continuously, with polyethylene-based resin (A) characterized by a comonomer distribution constant greater than 45, a recrystallization temperature between 85 ° C and 110 ° C, a tan delta value at 0.1 rad / s from 15 to 50 and a complex viscosity at 0.1 rad / s of 1400 Pa.s or less.
[0002]
Bicomponent fiber according to claim 1, characterized in that the fiber is a bicomponent fiber of the core-coating type, preferably an eccentric bicomponent fiber, and / or a bicomponent fiber of the side-to-side type.
[0003]
Two-component fiber according to claim 1, characterized by the fact that the polyethylene-based resin (A) has a differential scanning calorimetry (DSC) melting peak within the temperature range of 85 ° C to 110 ° C .
[0004]
Two-component fiber, according to claim 1, characterized by the fact that the polyethylene-based resin (A) has a comonomer distribution constant greater than 50.
[0005]
Two-component fiber, according to claim 1, characterized by the fact that the polyethylene-based resin (A) has a comonomer distribution constant in the range of 45 to 400.
[0006]
Two-component fiber, according to claim 1, characterized by the fact that the polyethylene-based resin (A) has a melting index (measured according to ASTM D 1238, condition 190 ° C / 2.16 kg) at range from 5 to 25 g / 10 min.
[0007]
Two-component fiber according to claim 1, characterized by the fact that the polyethylene-based resin (A) has a density in the range of 0.910 to 0.930 g / cm3.
[0008]
Two-component fiber according to claim 1, characterized by the fact that the polyethylene-based resin (A) has a recrystallization peak temperature in the range of 90 ° C to 105 ° C.
[0009]
Two-component fiber according to claim 1, characterized by the fact that the polyethylene-based resin (A) has more than 0.2 long chain branches / 1000 carbon atoms.
[0010]
Two-component fiber according to claim 1, characterized by the fact that the polyethylene-based resin (A) has a complex viscosity at 100 rad / s of 500 Pa.s or less.
[0011]
Two-component fiber, according to claim 1, characterized by the fact that the polyester-based resin (A) has a complex viscosity at 0.1 rad / s in the range of 500 to 1200 and at 100 rad / s in the range of 150 to 450 Pa.s.
[0012]
Two-component fiber according to claim 1, characterized by the fact that the polyethylene-based resin (A) has a tan delta value at 0.1 rad / s from 15 to 40.
[0013]
Two-component fiber according to claim 1, characterized by the fact that the high melting point resin (B) has a higher melting point than that of polyethylene-based resin (A) at least 20 ° C.
[0014]
Two-component fiber according to claim 1, characterized by the fact that the high melting point resin (B) is a polyolefin.
[0015]
Two-component fiber according to claim 14, characterized by the fact that the high melting point resin (B) is a polymer based on propylene.
[0016]
Two-component fiber, according to claim 1, characterized by the fact that the high melting point resin (B) is a polyester resin, being one of the group composed of polyethylene terephthalate (PET), polybutylene terephthalate (PBT) and polyphthalene terephthalate (PEN).
[0017]
Two-component fiber according to claim 1, characterized by the fact that the high melting point resin (B) is a polyamide resin.
[0018]
Two-component fiber according to claim 1, characterized by the fact that the polyethylene-based resin (A) and / or the high melting point resin (B) contains additives, one of the group consisting of coloring material, stabilizer of resistance thermometer, lubricant, nucleating agent and adhesion promoters.
[0019]
Two-component fiber according to claim 18, characterized by the fact that the adhesion promoter is maleic acid (MSA) or maleic acid anhydride (MAH), in amounts of 0.05 to 3% by weight.
[0020]
Two-component fiber, according to claim 1, characterized by the fact that the passage is from 0.7 to 20 dtex.
[0021]
Two-component fiber according to claim 1, characterized by the fact that the fiber is a cut fiber having a length of 0.2 cm to 15 cm.
[0022]
Two-component fiber, according to claim 1, characterized by the fact that the fiber is textured, said fiber having a stretch contraction (K1) of 3 to 7% and a number of corrugations of 3 to 6 corrugations / cm.
[0023]
Two-component fiber, according to claim 1, characterized by the fact that the fiber is textured, said fiber having a stretch contraction (K1) of 8 to 15% and a number of corrugations of 5 to 8 corrugations / cm.
[0024]
Non-woven, characterized by the fact that it comprises bicomponent fiber, as defined in any one of claims 1 to 23.
[0025]
Nonwoven according to claim 24, characterized by the fact that said nonwoven is a wetlaid nonwoven, an air-laid nonwoven or carded nonwoven.
[0026]
Nonwoven, according to claim 24, characterized by the fact that said nonwoven contains other fibrous materials, being an organic and / or inorganic fibrous material.
[0027]
Nonwoven according to claim 24, characterized by the fact that said nonwoven has a base weight of 10 to 500 g / m2.
[0028]
Non-woven fabric according to claim 24, characterized in that said bicomponent fiber is a continuous fiber or cut fibers, having a length of the cut fiber of 0.2 to 8 cm.
[0029]
Non-woven fabric according to claim 24, characterized in that said non-woven fabric is a wetlaid non-woven fabric and said bicomponent fiber is a non-textured flat fiber having a length of 0.2 cm to 3 cm .
[0030]
Non-woven, according to claim 24, characterized by the fact that said non-woven is an airlaid non-woven and said bicomponent fiber is textured, having a stretch contraction (K1) of 3 to 7% and the number of dimples of 3 to 6 dimples / cm, having a length of 0.2 to 3 cm.
[0031]
Non-woven fabric, according to claim 24, characterized by the fact that said non-woven fabric is a carded non-woven fabric and said bicomponent fiber is textured, having a stretch contraction (K1) of 8 to 15% and the number of dimples of 5 to 8 dimples / cm, having a length of 2 cm to 15 cm.
[0032]
Nonwoven, according to claim 24, characterized by the fact that said nonwoven also comprises particulate materials, being superabsorbent materials, said particulate materials being an inorganic particulate material, being a grinding material.
[0033]
Non-woven fabric according to claim 26, characterized by the fact that said fibrous organic material comprises, in addition to organic polymer resins, also fibrous natural materials.
[0034]
Non-woven fabric according to claim 33, characterized by the fact that said organic polymer resins are a reliable melt material, one of the group composed of polyolefins, polyesters, polyamide or a mixture of them.
[0035]
Non-woven fabric according to claim 26, characterized by the fact that said fibrous inorganic material is based on glass and / or minerals.
[0036]
Non-woven fabric according to claim 26, characterized by the fact that said fibrous organic material is based on cellulose, cotton, homo and copolymers based on polyethylene or polypropylene.
[0037]
Textile product, in particular sanitary and / or hygiene products, characterized by the fact that it comprises bicomponent fibers, as defined in any one of claims 1 to 23, and / or at least one non-woven, as defined in any one of the claims 24 to 36.
[0038]
Filter media products, characterized by the fact that they comprise bicomponent fibers, as defined in any one of claims 1 to 23, and / or at least one nonwoven, as defined in any one of claims 24 to 36.
[0039]
Battery separator products, characterized by the fact that they comprise bicomponent fibers, as defined in any one of claims 1 to 23, and / or at least one nonwoven, as defined in any one of claims 24 to 36.

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法律状态:
2018-04-10| B06F| Objections, documents and/or translations needed after an examination request according art. 34 industrial property law|

2019-02-19| B06T| Formal requirements before examination|

2020-01-07| B06A| Notification to applicant to reply to the report for non-patentability or inadequacy of the application according art. 36 industrial patent law|

2020-04-07| B06A| Notification to applicant to reply to the report for non-patentability or inadequacy of the application according art. 36 industrial patent law|

2020-08-25| B09A| Decision: intention to grant|

2021-01-26| B16A| Patent or certificate of addition of invention granted|Free format text: PRAZO DE VALIDADE: 10 (DEZ) ANOS CONTADOS A PARTIR DE 26/01/2021, OBSERVADAS AS CONDICOES LEGAIS. |

优先权:

申请号 | 申请日 | 专利标题

US12/651,628|US8389426B2|2010-01-04|2010-01-04|Bicomponent fiber|

US12/651,628|2010-01-04|

PCT/EP2010/008001|WO2011079959A1|2010-01-04|2010-12-31|New bicomponent fiber|

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