Classifications

• • D—TEXTILES; PAPER
  • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
  • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
  • D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
  • D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
  • D01F8/06—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyolefin as constituent
• • D—TEXTILES; PAPER
  • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
  • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
  • D01D5/00—Formation of filaments, threads, or the like
  • D01D5/28—Formation of filaments, threads, or the like while mixing different spinning solutions or melts during the spinning operation; Spinnerette packs therefor
  • D01D5/30—Conjugate filaments; Spinnerette packs therefor
• • D—TEXTILES; PAPER
  • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
  • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
  • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
  • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
  • D04H1/54—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving
• • D—TEXTILES; PAPER
  • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
  • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
  • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
  • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
  • D04H1/54—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving
  • D04H1/541—Composite fibres, e.g. sheath-core, sea-island or side-by-side; Mixed fibres
  • D04H1/5412—Composite fibres, e.g. sheath-core, sea-island or side-by-side; Mixed fibres sheath-core
• • D—TEXTILES; PAPER
  • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
  • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
  • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
  • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
  • D04H1/54—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving
  • D04H1/542—Adhesive fibres
  • D04H1/544—Olefin series
• • D—TEXTILES; PAPER
  • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
  • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
  • D04H13/00—Other non-woven fabrics
• • D—TEXTILES; PAPER
  • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
  • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
  • D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
  • D04H3/005—Synthetic yarns or filaments
  • D04H3/007—Addition polymers
• • D—TEXTILES; PAPER
  • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
  • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
  • D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
  • D04H3/08—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
  • D04H3/16—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with bonds between thermoplastic filaments produced in association with filament formation, e.g. immediately following extrusion
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
  • Y10T428/2913—Rod, strand, filament or fiber
  • Y10T428/2929—Bicomponent, conjugate, composite or collateral fibers or filaments [i.e., coextruded sheath-core or side-by-side type]
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
  • Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
  • Y10T442/637—Including strand or fiber material which is a monofilament composed of two or more polymeric materials in physically distinct relationship [e.g., sheath-core, side-by-side, islands-in-sea, fibrils-in-matrix, etc.] or composed of physical blend of chemically different polymeric materials or a physical blend of a polymeric material and a filler material
  • Y10T442/641—Sheath-core multicomponent strand or fiber material

Definitions

• the present invention relates to bicomponent fibers with improved bonding properties.
• the present invention relates to bicomponent fibers comprising an exterior component, which in turn comprises a polypropylene that has been degraded from a first melt flow index MFI 1 (measured according to ISO 1133, condition L, 230°C, 2.16 kg) to a second melt flow index MFI 2 (measured according to ISO 1133, condition L, 230°C, 2.16 kg), such that the degradation ratio MFI 1 /MFI 2 is within a well-defined range and such that the second melt flow index MFI 2 is in the range from 50 dg/min to 300 dg/min.
• the present invention relates to nonwovens, composites and laminates comprising said bicomponent fibers.
• the present invention also relates to a process for making such bicomponent fibers, nonwovens, composites and laminates.
• Polypropylene is one of the most widely used synthetic polymers for fibers and nonwovens because it has good mechanical and chemical properties and can be easily processed. Usually, the production of polypropylene fibers and nonwovens is done by a melt extrusion process, wherein molten polypropylene is extruded through a number of fine capillaries to form fibers or filaments, which can then be collected to form a nonwoven.
• polypropylene fibers and nonwovens need to have certain properties.
• fibers and nonwovens used in baby diapers should at the same time be strong, and also have a soft touch and good nonwoven forming properties, such as good thermal bonding behavior.
• Bicomponent fibers and nonwovens are made of an exterior component and an interior component with the interior component being largely covered by the exterior component.
• Such an arrangement allows producing fibers and nonwovens wherein the interior component provides the mechanical strength, and the exterior component provides the thermal bonding properties and/or the soft touch etc. This is exemplified by bicomponent fibers and nonwovens having a polypropylene as interior component and a polyethylene as exterior component.
• fibers and nonwovens comprising polyethylene have the disadvantage that they are more difficult to produce because the processability of polyethylene in fiber spinning is not as good as that of polypropylene.
• fibers and nonwovens that are mono-material, i.e. that are made from polypropylene only.
• the bicomponent fibers and nonwovens comprise an exterior component, which in turn comprises a polypropylene having specific properties.
• the present invention therefore provides a bicomponent fiber comprising
• the present invention further provides spunbond nonwovens, composites and laminates comprising such bicomponent fibers.
• the present invention provides a process for the production of bicomponent fibers comprising the steps of
• the present invention provides a process for the production of nonwovens, composites and laminates comprising the bicomponent fibers of the present invention.
• fiber and “filament” may be used interchangeably.
• the bicomponent fibers of the present invention comprise an exterior component and an interior component.
• the exterior component covers at least 50 % of the surface of the bicomponent fibers. More preferably it covers at least 70 %, even more preferably at least 90 %, 95 %, 97 % or 99 % and most preferably 100 % of the surface.
• Bicomponent fibers are known in many different configurations, such as for example side-by-side, sheath-core, islands-in-the-sea, pie or stripe configurations.
• Bicomponent fibers can be formed by co-extrusion of two different components into one fiber or filament. This is done by separately feeding the components to two extruders and combining the melts (or extrudates) into a single fiber or filament. The resulting fiber or filament has two different, essentially continuous polymer phases.
• Such fibers, their production as well as their forming a nonwoven, are well known to the skilled person and are for example described in F. Fourné, Synthetician Fasern, Carl Hanser Verlag, 1995, chapter 5.2 or in B.C. Goswami et al., Textile Yarns, John Wiley & Sons, 1977, p. 371 - 376 .
• the exterior component of said component fiber comprises a polypropylene.
• the exterior component comprises at least 50 wt%, more preferably at least 70 wt% or 90 wt%, even more preferably at least 95 wt% or 97 wt% or 99 wt% of polypropylene relative to the total weight of the exterior component; it is most preferred that the exterior layer consists of polypropylene.
• the polypropylene used in the exterior component may be produced by polymerizing propylene and one or more optional comonomers as defined below in the presence of a Ziegler-Natta catalyst system.
• catalyst systems are well known to the person skilled in the art. They comprise a titanium compound having at least one titanium-halogen bond and an internal electron donor, both on a suitable support (for example on a magnesium halide in active form), an organoaluminium compound (such as an aluminium alkyl), and an optional external donor (such as a silane or a diether compound).
• the polymerization of propylene and one or more optional comonomers can be carried out in a slurry, bulk or gas phase process.
• a slurry process the polymerization is carried out in a diluent, such as an inert hydrocarbon.
• a bulk process the polymerization is carried out in liquid propylene as reactor medium.
• the polypropylene recovered from the polymerization reactor is degraded either by thermal or by chemical treatment. Degradation by chemical treatment is preferred (“visbreaking").
• a peroxide for example with 2,5-dimethylhexane-2,5-di-tert-butylperoxide
• the melt flow of the polypropylene increases and the molecular weight distribution narrows.
• Visbreaking of polypropylene is generally carried out at temperatures in the range from 200°C to 250°C. It can for example be done in the extruder in the granulation step of a polypropylene manufacturing plant or in the extruder feeding a fiber or nonwoven production line.
• the degree to which a polypropylene has been degraded can be described by the degradation ratio MFI 1 /MFI 2 , which is the ratio between a first melt flow index MFI 1 (measured according to ISO 1133, condition L, 230°C, 2.16 kg) before degradation and a second melt flow index MFI 2 (measured according to ISO 1133, condition L, 230°C, 2.16 kg) after degradation.
• the polypropylene used in the exterior component of the present invention has a degradation ratio MFI 1 /MFI 2 of at least 0.1, preferably at least 0.12, more preferably at least 0.14, even more preferably of at least 0.16, still even more preferably of at least 0.18, and most preferably at least 0.20.
• the polypropylenes used in the present invention have a degradation ratio MFI 1 /MFI 2 of at most 0.8, more preferably of at most 0.7, even more preferably of at most 0.6, and most preferably of at most 0.5.
• the second melt flow index MFI 2 (measured according to ISO 1133, condition L, 230°C, 2.16 kg) of the polypropylenes used in the exterior component is at least 50 dg/min, preferably at least 55 dg/min, and most preferably at least 60 dg/min.
• the second melt flow index MFI 2 of the polypropylenes used in the present invention is at most 300 dg/min, preferably at most 200 dg/min, more preferably at most 150 dg/min and most preferably at most 100 dg/min.
• the interior component of said bicomponent fiber comprises a thermoplastic polymer that adheres to polypropylene.
• said thermoplastic polymer is a polypropylene.
• said thermoplastic polymer is a polypropylene that is different from the polypropylene comprised in the exterior component.
• the interior component comprises at least 50 wt%, more preferably at least 70 wt% or 90 wt%, even more preferably at least 95 wt% or 97 wt% or 99 wt% of said thermoplastic polymer relative to the total weight of the interior component; it is most preferred that the interior layer consists of said thermoplastic polymer.
• the polypropylene suitable for use in the interior component has a melt flow index (measured according to ISO 1133, condition L, 230°C, 2.16 kg) in the range from 5 dg/min to 500 dg/min.
• the polypropylene used in the interior component preferably has a melt flow index in the range from 5 dg/min 40 dg/min.
• the polypropylene used in the interior component preferably has a melt flow index of at least 10 dg/min, more preferably of at least 15 dg/min and most preferably of at least 20 dg/min; preferably the melt flow index is at most 300 dg/min, more preferably at most 200 dg/min, even more preferably at most 100 dg/min and most preferably at most 60 dg/min.
• the polypropylene suitable for use in the interior component has a molecular weight distribution (M w /M n ) in the range from 2.0 to 8.0, more preferably in the range from 2.0 to 5.0.
• M w /M n molecular weight distribution
• Such a polypropylene can for example be produced with a metallocene catalyst or with a Ziegler-Natta catalyst.
• the molecular weight distribution is reduced by thermal or chemical post-reactor treatment, for example by degradation with a peroxide ("visbreaking").
• Molecular weights may be determined by size exclusion chromatography (SEC) as described in the examples.
• polypropylenes used in the present invention can either be homopolymers or random copolymers of propylene with one or more comonomers. Homopolymers are preferred.
• the comonomers can be ethylene or a C 4 - C 20 ⁇ -olefin, such as for example butene-1, pentene-1, hexene-1, octene-1 or 4-methyl-pentene-1.
• the preferred random copolymer is a copolymer of propylene and ethylene.
• the random copolymers of the present invention comprise at least 0.1 wt%, preferably at least 0.2 wt% and most preferably at least 0.5 wt% of comonomer. Preferably they comprise at most 6.0 wt%, more preferably at most 5.0 wt% and most preferably at most 4.0 wt% of comonomer.
• the polypropylenes used in the present invention are predominantly isotactic polypropylenes, meaning that they are characterized by high isotacticity, for which the content of mmmm pentads is a measure.
• the content of mmmm pentads is at least 95.0 % and most preferably at least 96.0 wt%.
• the isotacticity is determined by NMR analysis according to the method described by G.J. Ray et al. in Macromolecules, vol. 10, n° 4, 1977, p. 773-778 .
• the polypropylenes used in the present invention either in the exterior or the interior component may also contain additives such as, by way of example, antioxidants, light stabilizers, acid scavengers, lubricants, antistatic additives, and colorants.
• additives such as, by way of example, antioxidants, light stabilizers, acid scavengers, lubricants, antistatic additives, and colorants.
• the bicomponent fibers as described above may be comprised in nonwovens, particularly in thermally bonded nonwovens or in spunbond nonwovens. It is preferred that such nonwovens comprise at least 50 wt%, preferably at least 70 wt% or 90 wt%, more preferably at least 95 wt% and most preferably that they consist of the bicomponent fibers of the present invention.
• the bicomponent fibers and nonwovens in accordance with the present invention are characterized by no or at most very little improvement in softness as had been expected from the use of the higher melt flow polypropylene as exterior component.
• the nonwovens, especially the spunbond nonwovens, of the present invention show an increase of around 10 % in tenacity. It needs to be emphasized that the tenacity increase was observed in machine as well as in cross-machine direction when compared to nonwovens comprising fibers made from the polypropylene of the interior component only.
• the present inventors have also been surprised that the increase in tenacity that was observed on the nonwovens, especially the spunbond nonwovens, of the present invention was not accompanied by a decrease in elongation but on the contrary by an increase in elongational properties.
• the present invention allows the production of nonwovens that at the same time have improved tenacity and elongation, and this in machine as well as cross-machine direction.
• Nonwovens comprising the bicomponent fibers of the present invention may be used to form a composite of nonwoven layers or a laminate with film.
• a composite according to the present invention comprises a spunbond nonwoven layer (S) according to the present invention and/or a melt blown nonwoven layer (M).
• the composite can for example be of the SS, SSS, SMS, SMMSS or any other type.
• a laminate according to the present invention comprises a spunbond nonwoven layer (S) according to the present invention and a film layer (F)
• the laminate can be of the SF, SFS or any other type.
• the film is a polyolefin film.
• the film of said laminate may be a breathable barrier film, thus resulting in a laminate with breathable properties.
• the bicomponent fibers of the present invention as well as the nonwovens, composites and laminates comprising them are produced by methods well known to the person skilled in the art.
• a polypropylene composition comprising the polypropylene as defined above for the exterior component is molten in a first extruder.
• said polypropylene composition comprises at least 50 wt%, more preferably at least 70 wt% or 90 wt%, even more preferably at least 95 wt% or 97 wt% or 99 wt% of the polypropylene as defined above for the exterior component relative to the total weight of the exterior component; it is most preferred that the exterior layer consists of the polypropylene as defined above for the exterior component.
• thermoplastic polymer composition comprising a thermoplastic polymer as defined for the interior component is molten in a second extruder.
• said thermoplastic polymer composition comprises at least 50 wt%, more preferably at least 70 wt% or 90 wt%, even more preferably at least 95 wt% or 97 wt% or 99 wt% of said thermoplastic polymer as defined for the interior component relative to the total weight of the exterior component; it is most preferred that the interior layer consists of said thermoplastic polymer as defined for the interior component.
• the molten thermoplastic polymer composition is then extruded from a number of fine, usually circular, capillaries of a spinneret.
• the molten polypropylene composition is extruded from a number of fine openings surrounding said capillaries.
• the extrudates from capillary and corresponding fine opening (Depending upon the type or bicomponent fiber to be produced it can also mean the extrudates from one or more capillaries and one or more surrounding fine opening that are intended to form a single filament.) are then combined to form a single, usually circular, filament of an intermediate diameter, whereby the extruded polypropylene composition forms the exterior component and the extruded thermoplastic polymer composition forms the interior component.
• the intermediate diameter of the filaments is rapidly reduced to a final diameter (drawing step).
• the fibers can be drawn over heated rolls or in a heated oven to further reduce the intermediate diameter to a final diameter and increase the tenacity of the fibers. If no further drawing step is performed the intermediate diameter is the final diameter.
• the production of bicomponent fibers is for example described in F. Fourné, Synthetician Fasern, Carl Hanser Verlag, 1995, chapter 5.2 or in B.C. Goswami et al., Textile Yarns, John Wiley & Sons, 1977, p. 371 - 376 .
• the nonwovens comprising the bicomponent fibers of the present invention may be produced either by thermal bonding of the bicomponent fibers of the present invention or by the spunbonding process.
• the nonwovens of the present invention are produced by the spunbonding process.
• the nonwovens are produced by collecting the bicomponent fibers of the present invention on a support and subsequently bonding the collected fibers to form a bonded nonwoven.
• the bicomponent fibers of the present invention are cut into staple fibers having a length in the range from 5 to 30 mm. Said staple fibers are then carded, i.e. collected as a more or less continuous non-consolidated web on a support. In a final step the non-consolidated web is consolidated by thermal or chemical bonding, with thermal bonding being preferred.
• fiber formation can be accomplished either by using one single spinneret with a large number of holes, generally several thousand, or by using several smaller spinnerets with a correspondingly smaller number of holes per spinneret.
• the combined extrudates with the polypropylene composition forming the exterior component and the thermoplastic polymer composition forming the interior component are quenched by a current of cold air.
• the diameter of the filaments is then rapidly reduced to a final diameter by a stream of high-pressure air.
• Air velocities in the drawdown step can be of several thousand meters per minute.
• the filaments are collected on a support, for example a wire mesh belt, thus creating a first fabric, which may then be passed through compaction rolls and finally goes through a bonding step. Bonding of the fabric may be accomplished by thermobonding, hydroentanglement, needlepunching, or chemical bonding.
• the fibers of the present invention proved very easy to process. No problems were encountered in the production of the nonwovens, especially the spunbond nonwovens, comprising the bicomponent fibers of the present invention.
• the bicomponent fibers and nonwovens of the present invention proved to also have the advantage of being more easily produced that fibers and nonwovens made from a commercial polypropylene of melt flow index 25 dg/min (measured according to ISO 1133, condition L, 230°C, 2.16 kg) and of narrow molecular weight distribution. Without wishing to be bound by theory it is believed that this is due to the higher melt flow index of the polypropylene used in the exterior component of the bicomponent fibers and nonwovens of the present invention.
• the higher melt flow index of the polypropylene in the exterior component does not lead to a loss in mechanical properties of the bicomponent nonwovens of the present invention when comprised of fibers having comparable titer but rather to an increase in both, tenacity and elongational properties in both directions, machine and cross-machine direction.
• One or more nonwovens in accordance with the present invention may be applied to one or more other nonwovens, which may but need not be in accordance with the present invention, to form a composite as described above.
• the one or more other nonwovens are thermally bonded nonwovens, spunbond nonwovens or melt blown nonwovens. Spunbond nonwovens are most preferred.
• One of more nonwovens in accordance with the present invention may be laminated to a film to form a laminate.
• the film preferably is a polyolefin film.
• the film may be a breathable barrier film, thus resulting in a laminate with breathable properties.
• the fibers, nonwovens, composites and laminates of the present invention may be used in hygiene articles, such as baby diapers, adult incontinence products, female hygiene products, and wipes, or in products for the construction industry or for agriculture, or for medical drapes and gowns, protective garments, lab coats etc.
• the melt flow index was measured according to norm ISO 1133, condition L, using a weight of 2.16 kg and a temperature of 230°C.
• the isotacticity (mmmm %) is determined by NMR analysis according to the method described by G.J. Ray et al. in Macromolecules, vol. 10, n° 4, 1977, p. 773-778 . It is performed on the dried product resulting of the extraction by boiling heptane of the xylene insoluble PP fraction.
• Nonwovens were produced using a polypropylene homopolymer, denoted as PP1, and a commercial polypropylene homopolymer, denoted as PP2.
• PP1 polypropylene homopolymer
• PP2 polypropylene homopolymer
• Polypropylenes PP1 and PP2 were used to produce the following spunbond nonwovens Example 1 - Bicomponent nonwoven with PP1 as exterior component and PP2 as interior component wherein the exterior layer comprised 30 wt% of the total weight of the fibers Comparative example 1 - Nonwoven made from PP2
• the spunbond nonwovens were produced on a 1.1 m wide Reicofil 4 line with a single beam having about 6800 holes per meter length, the holes having a diameter of 0.6 mm..
• the nonwoven had a fabric weight of 12 g/m 2 .
• the nonwoven were thermally bonded using an embossed roll. Further processing conditions are given in table 2.
• the bonding roll temperature reported in table 2 is the bonding temperature at which the highest values for elongation were obtained. Properties of the nonwoven obtained under these conditions are shown in table 3.
• the results show that the fibers and nonwovens in accordance with the present invention have improved properties in comparison to the fibers and nonwovens of the prior art.
• the present invention further allows the production of bicomponent fibers and nonwovens based on polypropylene only, without having to revert to the use of polyethylene in the exterior component, thus facilitating the production of such bicomponent fibers and nonwovens.

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• 2008
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  • 2009-07-29 US US13/055,013 patent/US20110189916A1/en not_active Abandoned
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