AU693536B2 - Highly crimpable conjugate fibers and nonwoven webs made therefrom - Google Patents

Highly crimpable conjugate fibers and nonwoven webs made therefrom Download PDF

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AU693536B2
AU693536B2 AU20425/95A AU2042595A AU693536B2 AU 693536 B2 AU693536 B2 AU 693536B2 AU 20425/95 A AU20425/95 A AU 20425/95A AU 2042595 A AU2042595 A AU 2042595A AU 693536 B2 AU693536 B2 AU 693536B2
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fibers
conjugate
fiber
ethylene
conjugate fiber
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AU2042595A (en
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Simon Kwame Ofosu
Ty Jackson Stokes
Alan Edward Wright
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Kimberly Clark Worldwide Inc
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Kimberly Clark Worldwide Inc
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    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING 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
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-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
    • D04H1/54Non-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
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/02Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/04Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/28Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/30Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising olefins as the major constituent
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F8/00Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
    • D01F8/04Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
    • D01F8/06Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyolefin as constituent
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING 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
    • D04H3/00Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/08Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
    • D04H3/16Non-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

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nonwoven Fabrics (AREA)
  • Multicomponent Fibers (AREA)
  • Cleaning Implements For Floors, Carpets, Furniture, Walls, And The Like (AREA)
  • Collation Of Sheets And Webs (AREA)
  • Filtering Materials (AREA)
  • Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
  • Artificial Filaments (AREA)

Description

Docket 11,219 Highly Crimpable Conjugate Fibers and Nonwoven Webs Made Therefrom BACKGROUND OF THE INVENTION The present invention is related to conjugate fibers containing a high melt flow rate propylene polymer and to nonwoven webs produced therefrom.
Conjugate fibers having two or more of component polymers that are designed to benefit from combinations of desired chemical and/or physical properties of the component polymers are well known in the art. Methods for making conjugate fibers and fabrics made therefrom are disclosed, for example, in U.S. Patents 3,423,266 to Davies et al., Reissue 30,955 to Stanistreet and European Patent Application 0 586 924.
In addition to providing combined desirable properties of component polymers, conjugate fibers can be thermally crimped, especially when the fibers are produced from component polymers that are different in crystallization, shrinkage and/or solidification properties, to improve tactile properties, including "cloth-like" texture, bulk and fullness, of nonwoven webs or fabrics made from the fibers. For example, European Patent Application 0 586 924 discloses thermally crimped conjugate fibers that are dimensionally stable.
Although processes for thermally crimping conjugate fibers are known in the art, it is also known that the process of thermally imparting crimps becomes highly onerous as the thickness of fibers gets smaller.
Consequently, small denier fibers tend to form flat or dense nonwoven webs. Although thermally crimped finedenier conjugate fibers can be produced by significantly reducing the throughput, the amount of polymer processed through a spinneret, or by increasing the processing temperature of the polymer components, neither of the alternatives is commercially desirable. Reducing the throughput rate decreases the production rate of the fibers and increasing the polymer processing temperature 2 creates processing difficulties, thermal degradation of the polymers, and heightens the quenching requirement of the spun fibers.
It is highly desirable to provide a method of producing highly crimpable conjugate fibers that can be processed to have high levels of crimps even at fine deniers and that does not require complicated and/or onerous manufacturing steps, and it is also highly desirable to provide nonwoven webs made from such fibers.
Summary of the Invention There is disclosed herein a highly crimpable conjugate fiber comprising: a propylene polymer component and an ethylene polymer component, wherein said polypropylene polymer component comprises a polypropylene polymer having a melt flow rate between 50 g/10 min. and 200 g/10 min. as measured in accordance with ASTM D1238, Testing Condition 2302/2.16 and is selected from homopolymers and copolymers of propylene and blends thereof, and wherein the ethylene polymer component comprises an ethylene polymer which is selected from homopolymers and copolymers of ethylene.
There is further disclosed herein a lofty nonwoven fabric having a bulk of at least 0.015 mm/g/m 2 and comprising crimped conjugate spunbond fibers, said conjugate spunbond fibers having a weight per unit length equal to or less than 2.5 denier and comprising the above disclosed conjugate 'iber, wherein each of said components 20 occupies a distinct section of substantially the entire length of said spunbond fiber.
The present conjugate fibers are highly crimpable even at fine deniers, providing a soft, high loft nonwoven web. As such, the nonwoven webs produced from the conjugate fibers are highly useful as various parts for disposable articles, including diapers, sanitary napkins, incontinence products, wipes, cover materials, garment 25 materials and the like, and filters.
The term "conjugate fibers" refers to fibers containing at least two polymeric Scomponents which are arranged to occupy distinct sections for substantially the entire length of the fibers. The conjugate fibers are formed by simultaneously extruding at S: least two molten polymeric component compositions as a plurality of unitary multicomponent filaments or fibers from a plurality of capillaries of a spinneret. The term "spunbond fiber web" refers to a nonwoven fiber web of small diameter filaments or fibers that are formed by extruding or melt-spinning /^4J -o 4' "o IN ILIBDLL0143KEH molten thermoplastic polymers as filaments or fibers from a plurality of capillaries of a spinneret. The extruded filaments are partially cooled and then rapidly drawn by an eductive or other well-known drawing mechanism. The drawn filaments are deposited or laid onto a forming surface in a random, isotropic manner to form a loosely entangled fiber web, and then the laid fiber web is subjected to a bonding process to impart physical integrity and dimensional stability. Bonding processes suitable for spunbond fiber webs are well known in the art, which include calender bonding, ultrasonic bonding, hydroentangling, needlepunching and through air bonding processes. The production of spunbond webs is disclosed, for example, in U.S. Patents 4,340,563 to Appel et al.; o. 15 3,692,618 to Dorschner et al and European Patent Application 0 586 924 to Kimberly-Clark Corp. European Patent Application 0 586 924, which is herein incorporated by reference in its entirety, d.scloses a particularly suitable spunbond fiber web forming process for the present 20 invention. Typically, spunbond filaments or fibers have an average diameter in excess of 10 im and up to about im or higher, although finer spunbond fibers can be produced. The term "bonded carded staple fiber web" refers to a nonwoven web that is formed from staple fibers.
Staple fibers are conventionally produced with a meltspinning process, in which continuous fibers or filaments are produced and then cut to a staple length, often in the range of from about 1 inch to about 8 inches. The continuous fiber-forming steps of the process are typically similar to the melt-spinning steps of a conventional spunbond fiber web-forming process. The staple fibers are subsequently carded and bonded to form a nonwoven web.
BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 illustrates a suitable process for producing the conjugate fiber and the nonwoven web of the invention.
I- -Y DETAILED DESCRIPTION OF THE INVENTION The present invention provides a nonwoven fiber web of spunbond conjugate fibers or staple conjugate fibers that are highly crimpable even at fine deniers. The fiber web provides improved textural properties, including softness and bulk, as well as improved physical properties, such as web uniformity and coverage. The conjugate fibers of the present invention contain an ethylene polymer component and a propylene polymer component, although the conjugate fibers may contain additional polymer components that are selected from a wide variety of fiber-forming polymers.
Desirably, the conjugate fibers contain from about 20 wt% to about 80 wt% of an ethylene polymer and from about wt% to about 20 wt% of a propylene polymer, based on the 15 total weight of the fibers.
Suitable propylene polymers for the present invention are homopolymers and copolymers of propylene, which include isotactic polypropylene, syndiotactic polypropylene and propylene copolymers containing minor amounts of one or 20 more of other monomers that are known to be suitable for forming propylene copolymers, ethylene, butylene, methylacrylate-co-sodium allyl sulphonate, and styrene-costyrene sulphonamide. Also suitable are blends of these polymers. Additionally suitable propylene polymers are the above-mentioned propylene polymers blended with a minor amount of ethylene alkyl acrylate, ethylene ethyl acrylate; polybutylene; and/or ethylene-vinyl acetate. Of these suitable propylene polymers, more desirable are isotactic polypropylene and propylene copolymers containing up to about 10 wt% of ethylene. In accordance with the present invention, suitable propylene polymers have a melt flow rate higher than conventional fiber-forming polypropylenes. The melt flow rate of a suitable propylene polymer is equal to or higher than about 45 g/ 10 min. at 2300C, as measured in accordance with ASTM D-1238; and desirably, the melt flow rate is between about 50 and about 200 g/ 10 min at 230°C; more desirably, between about and about 175 g/ 10 min at 230 0 C and most desirably, the melt flow rate is between about 60 and about 150 g/ 10 min at 230 0 C. If the melt flow rate of the propylene polymer is lower than the specified range, it is difficult to produce highly crimped conjugate fibers of fine deniers, 2.5 denier or less, with a conventional fiber-forming process at commercial speed, and if the melt flow rate is higher than the specified umore desired range, the physical incompatibility of the component polymer melts may cause fiber-spinning difficulties and produce malformed fibers or fail the fiber-spinning process altogether. To a limited extent, the difficulties in spinning a propylene polymer having a melt flow rate higher than the specified range can be alleviated by employing an ethylene polymer having a 15 comparably high melt flow rate. Surprisingly, the present conjugate fibers containing a high melt flow rate propylene polymer can be thermally processed to contain high levels of crimps even at fine deniers and thus can be fabricated into lofty fabrics of fine denier fibers. For example, the conjugate fibers can be processed to provide a fiber web having a bulk of at least about 20 mils per ounce per square yard, as measured under a 0.025 psi load, even when the size of the fibers is reduced to about 2.5 denier or less, desirably to about 2 denier or less, and more desirably to about 1.5 denier.
Ethylene polymers suitable for the present invention are fiber-forming homopolymers of ethylene and copolymers of ethylene and one or more of comonomers, such as, butene, hexene, 4-methyl-i pentene and octene, ethylene-vinyl acetate and ethylene alkyl acrylate, ethylene ethyl acrylate, as well as blends thereof. The suitable ethylene polymers may be blended to contain a minor amount of ethylene alkyl acrylate, ethylene ethyl acrylate; polybutylene; and/or ethylene-vinyl acetate. More desirable ethylene polymers include high density polyethylene, linear low density polyethylene, medium density polyethylene, low density polyethylene and blends thereof; and most desirable ethylene polymers are high density polyethylene and linear low density polyethylene.
Fiber-forming polymers suitable for the additional polymer components of the present conjugate fibers include polyolefins, polyesters, polyamides, acetals, acrylic polymers, polyvinyl chloride, vinyl acetate-based polymer and the like, as well as blends thereof. Useful polyolefins include polyethylenes, high density polyethylene, medium density polyethylene, low density polyethylene and linear low density polyethylene; polypropylenes, isotactic polypropylene and syndiotactic polypropylene; polybutylenes, poly(lbutene) and poly(2-butene); polypentenes, poly(2pentene), and poly(4-methyl-l-pentene); and blends thereof.
S 15 Useful vinyl acetate-based polymers. include polyvinyl acetate; ethylene-vinyl acetate; saponified polyvinyl acetate, polyvinyl alcohol; ethylene-vinyl alcohol and blends thereof. Useful polyamides include nylon 6, nylon 6/6, nylon 10, nylon 4/6, nylon 10/10, nylon 12, hydrophilic polyamide copolymers such as caprolactam and alkylene oxide, ethylene oxide, copolymers and hexamethylene adipamide and alkylene oxide copolymers, and blends thereof. Useful polyesters include polyethylene terephthalate, polybutylene terephthalate, and blends thereof. Acrylic polymers suitable for the present invention include ethylene acrylic acid, ethylene i.ethacrylic acid, ethylene methyl methacrylate and the like as well as blends thereof. In addition, the fiber composition may further contain minor amounts of compatibilizing agents, colorants, pigments, optical brighteners, ultraviolet light stabilizers, antistatic agents, lubricants, abrasion resistance enhancing agents, crimp inducing agents, nucleating agents, fillers and other processing aids.
suitable conjugate fibers for the present invention may have a side-by-side or sheath-core configuration. When a sheath-core configuration is utilized, an eccentric sheath-core configuration, non-concentrically aligned sheath and core, is more desirable since eccentric sheathcore fibers are more amenable to thermal crimping processes. Suitable conjugate fibers can be produced with any known staple or continuous conjugate fiber forming process, for example, disclosed in U.S. Patents 3,423,266 to Davies et al., Reissue 30,955 to Stanistreet, 4,189,338 to Ejima et al. and European Patent Application 0 586 924.
As is known in the art, crimps in conjugate fibers can be imparted before, during or after the fibers are deposited or laid to form a nonwoven web. However, it is highly desirable to crimp the conjugate fibers before they are formed into a nonwoven web since the crimping process to 1 inherently causes shrinkage and dimensional changes. It is 15 to be noted that although the present invention is .00. illustrated with thermal crimping processes, any known mechanical crimping process can also be utilized.
Turning to Figure 1, the drawing illustrates a highly suitable process 10 for producing a highly suitable nonwoven conjugate fiber web, more specifically a bicomponent fiber web. A pair of extruders 12a and 12b separately extrude two polymeric compositions, which compositions are separately fed into a first hopper 14a and Ic °a second hopper 14b, to simultaneously supply molten polymeric compositions to a spinneret 18 through conduits 16a and 16b. Suitable spinnerets for extruding conjugate **1*Ie
I
fibers are well known in the art. Briefly, the spinneret 18 has a housing which contains a spin pack, and the spin pack contains a plurality of plates and dies. The plates have a pattern of openings arranged to create flow paths for directing the two polymers to the dies that have one or more rows of openings, which are designed in accordance with the desired configuration of the resulting conjugate fibers.
A curtain of fibers is produced from the rows of the die openings and is partially quenched by a quench air blower 20 before being fed into a fiber draw unit, or an aspirator, 22. The quenching process not only partially quenches the fibers but also develops a latent helical crimp in the fibers. Suitable fiber draw units or aspirators for use in melt spinning polymers are well known in the art, and particularly suitable fiber draw units for the present invention include linear fiber aspirators of the type disclosed in European Patent Application 0 586 924, published March 16, 1994, which is incorporated by reference. Briefly, the fiber draw unit 22 includes an elongate vertical passage through which the filaments are drawn by heated aspirating air entering from the side of the passage from a temperature adjustable heater 24. The hot aspirating air draws the filaments and ambient air *...through the fiber draw unit 22. The temperature of the air 15 supplied from the heater 24 is sufficient that, after some cooling due to mixing with cooler ambient air aspirated with the filaments, the air heats the filaments to a temperature required to activate the latent crimp. The temperature of the air from the heater can be varied to achieve different levels of crimp. In general, a higher air temperature produces a higher number of crimps.
The process line 10 further includes an endless S.foraminous forming surface 26 which is positioned below the fiber draw unit 22. The continuous fibers from the outlet of the draw unit are deposited onto the forming surface 26 in a random fashion to produce a continuous web of uniform
I
density and thickness. The fiber depositing process can be assisted by a vacuum unit 30 placed below the forming surface 26. Optionally, the resulting web can be subjected to a light compacting pressure with a roller 32 to consolidate the web to impart additional physical integrity to the web before being subjected to a bonding process.
The nonwoven web is then bonded, for example, by a through air bonding process. Generally described, a through air bonder 36 includes a perforated roller 38, which receives the web, and a hood 40 surrounding the perforated roller. Heated air, which is sufficiently high enough to melt the lower melting component polymer the conjugate fiber, is supplied to the web through the perforated roller 38 and withdrawn by the hood 40. The heated air melts the lower melting polymer and the melted polymer forms interfiber bonds throughout the web, especially at the points where the fibers cross over.
Through air bonding processes are particularly suitable for producing a lofty, uniformly bonded spunbond web since these processes uniformly effect interfiber bonds and do not utilize intermittently placed compacting pressures to effect interfiber bonds. Alternatively, the unbonded nonwoven web can be bonded with a calender bonder. A calender bonder is typically is an assembly of two or more of abuttingly placed heated rolls that apply a combination of heat and pressure to melt fuse the fibers of a thermoplastic nonwoven web, thereby effecting bonded regions or points in the web. The bonding rolls may be o. smooth to provide uniformly bonded nonwoven webs or contain a pattern of raised bond points to provide point bonded 20 webs.
The soft, high loft nonwoven web of the present invention are highly useful as disposable medical fabrics, surgical gowns, surgical drapes and sterile wrap; cover materials, automobile and boat covers; protective garments, coveralls, uniforms and aprons; *see*: and various parts for disposable and personal care 6 articles, e.g. diapers, training pants, sanitary napkins, incontinence products, wipes and the like. In addition, the present lofty nonwoven web that contains fine denier fibers and has a higher bulk and improved uniformity over conventional conjugate spunbond fiber webs is highly useful for filtration applications in that the web provides uniformly distributed finer interfiber pores without sacrificing the loft of the web.
The following examples are provided for illustration purposes and the invention is not limited thereto.
Examples: Examples 1-2 (Exl-Ex2) Point bonded spunbond fiber webs of round side-byside conjugate fibers containing 50 wt% linear low density polyethylene and 50 wt% polypropylene were produced using the process illustrated in Figure 1. The bicomponent spinning die had a 0.6 mm spinhole diameter, a 6:1 L/D ratio and a 50 holes/inch spinhole density. Linear low density polyethylene (LLDPE), Aspun 6811A, which is available from Dow Chemical, was blended with 2 wt% of a Tio 2 concentrate containing 50 wt% of TiO 2 and 50 wt% of polypropylene, and the mixture was fed into a first single screw extruder. The LLDPE composition was extruded to have a melt temperature of about 430OF as the extrudate exits 15 the extruder. Polypropylene, X11029-20-1, which has a melt flow rate (MFR) of about 65 g/ 10 min. at 230 0 C and is o .available from Himont, was blended with 2 wt% of the abovedescribed TiO 2 concentrate, and the mixture was fed into a second single screw extruder. The melt temperature of the 20 polypropylene composition was kept at 430°F for Example 1 and 465 0 F for Example 2. The LLDPE and polypropylene extrudates were fed into the spinning die which was kept at about 430 0 F, and the spinhole throughput rate was kept at 0.7 gram/hole/minute for Example 1 and 0.5 gram/hole/minute for Example 2. The bicomponent fibers exiting the spinning die were quenched by a flow of air having a flow rate of SCFM/inch spinneret width and a temperature of 65 0 F. The quenching air was applied about 5 inches below the spinneret. The quenched fibers were drawn and crimped in the aspirating unit using a flow of air heated to about 350°F and supplied to have a flow rate of 50.9 ft 3 /min/inch width. Then, the drawn, crimped fibers were deposited onto a foraminous forming surface with the assist of a vacuum flow to form an unbonded fiber web. The unbonded fiber web was bonded by passing the web through the nip formed by two abuttingly placed bonding rolls, a smooth anvil roll and a patterned embossing roll. The raised bond points of the 111- 1 1-~II-I ~lld- 1_11 embossing roll covered about 15% of the total surface area and there were about 310 regularly spaced bond points per square inch. Both of the rolls were heated to about 250 0
F
and the pressure applied on the webs was about 100 lbs/linear inch of width. The bonded nonwoven webs, which had an average weight of about 1.0 ounce per square yard (osy), were tested for their bulk and average fiber size.
The crimp level of the fibers forming the nonwoven webs was indirectly measured by comparing the bulk of the webs since the bulk is directly correlated to the crimp level of the fibers, and the bulk is measured in mils under a 0.025 psi load. The results are shown in Table 1.
Control 1-2 (C1-C2) 15 The procedure outlined for Examples 1 and 2 was repeated to produce Control 1-2, respectively, except Exxon PP3445 polypropylene was used. The polypropylene has a melt flow rate of about 35 g/ min. at 230 0 C and is a conventional fiber grade polypropylene. The results are 20 shown in Table 1.
25 Table 1 Polypropylene Throughput Example MFR Rate Fiber Size Bulk (g/min) (g/hole/min) (denier) (mil) Ex 65 0.7 2.5 20.3 Ex2 65 0.5 1.8 14.5 Cl 35 0.7 2.8 11.8 C2 35 0.5 1.8 11.0 The results demonstrate that the conjugate fibers containing a high melt flow polypropylene provide bulkier nonwoven fabrics, and thus the fibers contain a higher level of crimps than the conjugate fibers produced from a conventional spunbond fiber-forming fiber grade polypropylene. It is also to be noted that Cl and C2
I
exhibited similar bulk values even though the difference in the size of the fibers was highly significant, demonstrating the difficulty in thermally crimping fine denier fibers.
Example 3-7 (Ex3-Ex7) Unbonded nonwoven webs of side-by-side conjugate fibers were produced in accordance with the procedure outline in Example 1 using two different grades of polypropylene as indicated in Table 2, except the polymer throughput rate was kept at 0.7 g/hole/minute and the melt temperature of the two component polymer compositions was maintained at 430 0 F. In addition, the size of the fibers was controlled by changing the flow rate of heated air supplied to the aspirating unit as indicated in Table 2.
Both 100 melt flow rate and 65 melt flow rate polypropylene resins were obtained from Shell Chemical.
The unbonded nonwoven webs were then bonded by passing the webs through a through-air bonder. The bonder exposed the nonwoven webs to a flow of heated air having a temperature of about 270OF and a flow rate of about 200 feet/min. The average weight, fiber size and bulk of the bonded webs were measured, and the bulk was normalized to 1 osy. The results are shown in Table 2.
Control 3-5 Example 3 was repeated except the polypropylene employed was the 35 melt flow rate polypropylene disclosed in Control 1. The results are shown in Table 2.
Table 2 Flow Rate Fiber Example PP M4FR of Heated Air Size (g/min) (f t'/min/ (denier) inch width) Ex3 100 37.3 2.0 Ex4 65 37.3 2.5 Ex5 100 42.9 1.9 Ex6 100 48.6 1.8 Ex7 65 48.5 1.9 C3 35 37.3 2.5 C4 35 42.9 2.41 C5 35 44.5 2.0 Web Weight (osy) 2 .03 1.85 1.189 1.94 2 .18 1.95 2 .03 2 .12 Bulk (mil/osy) 36.5 37.2 37.4 23.7 23.6 19.5 14.5 14.3 0 0 *0e 20 9b 00 *000 *000 0 *0 0* The results clearly demonstrate that utilizing a high melt flow propylene polymer significantly improves the bulk of thie conjugate f iber webs. For example, although the fibers of Example 4 and Control 3 had the same fiber size, the bulk of Example 4 was about 91% loftier than that of Control 3.
*0 0 0 0*0 U 0000 0Y 0 0~ 4 @00 0 0000 0 0000

Claims (13)

1. A highly crimpable conjugate fiber comprising: a propylene polymer component and an ethylene polymer componert, wherein said polypropylene polymer component comprises a polypropylene polymer having a melt flow rate between 50 g/10 min. and 200 g/10 min. as measured in accordance with ASTM D1238, resting Condition 2302/2.16 and is selected from homopolymers and copolymers of propylene and blends thereof, and wherein the ethylene polymer component comprises an ethylene polymer which is selected from homopolymers and copolymers of ethylene. to
2. The conjugate fiber of claim 1 wherein said propylene polymer is selected from the group consisting of isotactic polypropylene and propylene copolymers containing up to 10 wt of ethylene.
3. The conjugate fiber of claim 1 wherein said conjugate fiber has a side-by- side configuration.
4. The conjugate fiber of claim 1 having an eccentric sheath-core configuration.
The conjugate fiber of claim 1 wherein said propylene polymer has a melt flow rate between 55 and 150 g/10 min.
6. The conjugate fiber of claim 1 wherein said propylene polymer is isotactic 20 polypropylene and said ethylene polymer is linear low density polyethylene.
7. A lofty nonwoven fabric having a bulk of at least 0.015 mm/g/m 2 and :comprising crimped conjugate spunbond fibers, said conjugate spunbond fibers having a weight per unit length equal to or less than 2.5 denier and comprising the conjugate fiber of any one of the preceding claims, wherein each of said components occupies a 25 distinct section of substantially the entire length of said spunbond fiber.
8. A disposable article comprising the lofty nonwoven fabric of claim 7. a.
9. A personal care article comprising the lofty nonwoven fabric of claim 7. S*
10. A disposable gown comprising the lofty nonwoven fabric of claim 7.
11. A filter comprising the lofty nonwoven fabric of claim 7. a. 30
12. A highly crimpable conjugate fiber, substantially as hereinbefore described with reference to any one of the Examples but excluding the Comparative Examples.
13. A lofty nonwoven fabric substantially as hereinbefore described with reference to any one of the Examples but excluding the Comparative Examples. Dated 4 May, 1998 Kimberly-Clark Corporation Patent Attorneys for the Applicant/Nominated Person SPRUSON FERGUSON IN.LIOLL1dt435:KEH I __I Highly Crimpable Conjugate Fibers and Nonwoven Webs Made Therefrom Abstract of the Invention The present invention provides conjugate fibers having an ethylene polymer component and a propylene polymer component, which are highly crimpable even at fine deniers. Also provided are nonwoven fabrics made from the fibers. The propylene polymer component of the conjugate fiber contains a propylene polymer having a melt flow rate equal to or higher than about 45 g/ 10 min. at 230 0 C. o* 0 .0 00
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EP1709224B2 (en) 2004-01-27 2016-10-12 The Procter and Gamble Company Soft extensible nonwoven webs containing multicomponent fibers with high melt flow rates
JP4897469B2 (en) * 2006-12-21 2012-03-14 パナソニック株式会社 Nonwoven fabric manufacturing apparatus and nonwoven fabric manufacturing method
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CZ201324A3 (en) * 2013-01-14 2014-07-23 Pegas Nonwovens S.R.O. Fiber layer comprising crimped bi- or multicomponent fibers and process for producing thereof
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EP0685579A2 (en) 1995-12-06
DE69506784T2 (en) 1999-05-20
KR960001222A (en) 1996-01-25
EP0685579B1 (en) 1998-12-23
KR100335729B1 (en) 2002-11-22
CA2136575A1 (en) 1995-12-04
CO4440450A1 (en) 1997-05-07
AU2042595A (en) 1995-12-14
EP0685579A3 (en) 1996-07-31
JP3850901B2 (en) 2006-11-29
ES2126806T3 (en) 1999-04-01
DE69506784D1 (en) 1999-02-04
BR9502630A (en) 1996-01-02
JPH0827625A (en) 1996-01-30

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