|Número de publicación||USRE35621 E|
|Tipo de publicación||Concesión|
|Número de solicitud||US 08/473,917|
|Fecha de publicación||7 Oct 1997|
|Fecha de presentación||7 Jun 1995|
|Fecha de prioridad||30 May 1989|
|Número de publicación||08473917, 473917, US RE35621 E, US RE35621E, US-E-RE35621, USRE35621 E, USRE35621E|
|Inventores||A. Chandler Schmalz|
|Cesionario original||Hercules Incorporated|
|Exportar cita||BiBTeX, EndNote, RefMan|
|Citas de patentes (52), Otras citas (8), Citada por (18), Clasificaciones (21), Eventos legales (11)|
|Enlaces externos: USPTO, Cesión de USPTO, Espacenet|
.Iadd.This application is a continuation of application Ser. No. 07/909,188, filed Jul. 6, 1992, now abandoned. .Iaddend.
The present invention relates to a method utilizing topically applied modifier compositions arranged in sequence and in a unique arrangement whereby polyolefin-containing hydrophobic fiber or filament is made receptive to interim cutting and carding operations without loss of hydrophobicity in the resulting fiber or nonwoven product.
While the manufacture of polyolefin-based fiber, webs and corresponding nonwoven materials are well known in the textile art, attempts to broadly apply such knowledge to produce products in the area of personal hygiene, such as catamenial devices, disposable diapers, incontinence pads and the like, have met with serious technical problems.
In general, such products must have a fluid-absorbent core, usually comprising one or more layers of absorbent material such as wood pulp, rayon, gauze, tissue and the like and, in some cases, synthetic hydrophilic material such as a hydrophilic polyurethane foam.
Such fluid-absorbing core is most generally fabricated in the form of a thermally bonded pad, of wood pulp, fiber and conjugate fiber, having a rectangular or somewhat oval shape. To protect a wearer's clothing, and surrounding areas from stain or wetting by fluids already absorbed in such a core, a fluid-impervious barrier sheet is usually required. In general, the absorbent device is positioned against the body of the user with hydrophilic material facing and contacting the body and the fluid impervious barrier sheet positioned on the outside or opposite side.
A particularly troublesome technical problem arises when a high degree of hydrophobicity is desired in a nonwoven component produced substantially from conventionally bonded webs of hydrophobic fiber such as polyolefin-containing staple or spun-bonded webs.
In general, untreated hydrophobic fiber quickly becomes unworkable due to friction and accumulated static charge generated during conventional spinning, cutting and carding operations. For this reason, the art has long recognized and used a variety of topically applied antistatic agents which change fiber surface properties sufficiently to permit such conventional fiber processing. In effect, however, such treatment also produces fiber, web and nonwoven product which is substantially more hydrophilic than the untreated spun fiber.
Because of the nature of commercial high speed operations, and the somewhat unpredictable affinity of such agents to individual batches or bales of hydrophobic fiber, it becomes very difficult to maintain adequate control over bonding steps and over the wetting characteristics of the final nonwoven product.
It is an object of the present invention to prepare a hydrophobic polyolefin-containing spun fiber or filament for processing such as intermediate cutting and carding steps without unduly interfering with subsequent bonding steps or sacrificing needed hydrophobic characteristics in the nonwoven product.
The above objects are obtained in accordance with the present invention by preparing polyolefin-containing spun fiber or filament in accordance with the steps of
A. initially treating the corresponding continuous spun fiber or filament with an effective amount, varying from about0.09%-0.5% based on fiber weight, of a first modifier composition comprising
(a) about 70%-100% by weight of modifier composition of at least one neutralized phosphoric acid ester represented by the formula ##STR1## wherein Alk is individually defined as a lower alkyl group, such as a 1-8 carbon alkyl and preferably a 1-4 carbon alkyl group;
R is defined as an amino group or an alkali metal,
n and m are individually defined as positive numbers of not less than about 1, the sum of which is about 3; and
(b) up to about 30% by weight of modifier composition of at least one polysiloxane represented by the formula ##STR2## wherein X and Y are individually defined as a hydrophobic chemical end group such as a lower alkyl group;
R' is individually defined as a lower alkyl such as a methyl group, and
o is defined as a positive number within the range of about 10-50 or higher;
B. crimping the resulting continuous fiber or filament in a crimper;
C. applying to said continuous fiber or filament preferably at a point proximate to said crimper an effective amount, varying from about 0.05%-0.20% by fiber weight, of a second modifier composition comprising
(a) about 70%-100%, by weight of second modifier composition, of at least one polysiloxane represented by formula (2), and
(b) up to about 30%, by weight of second modifier composition, of at least one neutralized phosphoric acid ester represented by formula (1);
D. processing the resulting modifier-treated continuous fiber or filament, for spun bonding or for staple web bonding purposes, to obtain position one or more webs for bonding; and
E. bonding the resulting web in a conventional manner to obtain a desired hydrophobic nonwoven material.
For present purposes the term "polyolefin-containing spun fiber or filament" includes continuous as well as staple melt spun fibers which are obtainable from conventionally blended isotactic polypropylene as well as art-recognized hydrophobic copolymers thereof with ethylene, 1-butene, 4-methylpentene-1 and the like. The resulting blended . .an.!. .Iadd.and .Iaddend.extruded spun melt conveniently has a weight average varying from about 3×105 to about 5×105, a molecular weight distribution of about 5.0-8.0, a melt flow rate of about 2.5 to about 4.0 g/10 minutes, and a spin temperature conveniently within a range of about 220° C.-300° C.
Also includible within the spun melt are various art-recognized fiber additives, including pH stabilizers such as calcium stearate, antioxidants, pigments, including whiteners and colorants such as TiO2 and the like. Generally such additives vary, in amount, from about 0.5%-3% by weight of spun melt.
The present invention is found particularly applicable to high speed production of a variety of nonwoven materials utilizing webs obtained, for instance, from spun bonded or carded staple and may also comprise additional web components such as . .fabricated.!. .Iadd.fibrillated .Iaddend.film and the like. In each case, the fiber-handling difficulties generated by friction and accumulated static charge can be avoided, without unacceptable sacrifice in bonding characteristics (i.e. strength) or loss of hydrophobic properties of the final nonwoven product.
In this regard, the term "processing" as applied in process step "D" is inclusive of art recognized web formation techniques applicable to continuous as well as crimped, cut and carded staple fiber, the crimping step in the former case being optional with respect to webs formed solely of fiber or filament.
Continuous spun fiber or filaments used to form webs within the scope of the present invention preferably comprise topically treated spun melt staple fiber, filament or fibrillated film of bicomponent or monofilament types, the above-defined modifier compositions being conventionally drawn over a feed wheel partially immersed in a bath of the above-defined modifier composition, dipped therein, or sprayed in effective amount for fiber processing, and dried.
For present purposes, webs used to form nonwovens within the scope of the present invention can be formed by spun bonded, melt blown or conventional "Dry" carded Process using staple fiber and bonded together using techniques employing adhesive binders (U.S. Pat. No. 4,535,013), calender rolls, hot air, sonic, laser, pressure bonding, needle punching and the like, known to the art.
Webs used to fabricate nonwoven material can also usefully comprise conventional sheath/core or side-by-side bicomponent fiber of filament, alone or combined with treated or untreated homogeneous type fiber or filament and/or fibrillated film.
Also within the scope of the present invention is the use of nonwovens comprised of one or more bonded webs of modifier-treated polyolefin fiber and/or fiber-like (fibrillated film) components having a mixed fiber denier of homogeneous and/or bicomponent types not exceeding about 40 dpf. Such webs preferably utilize fiber or filaments within a range of about 0.1-40 dpf.
In addition, the resulting nonwoven material can be embossed and/or calender printed conventionally with various designs and colors, as desired, to increase loft, augment wet strength, and provide easy market identification.
In addition, webs used in forming nonwovens within the scope of the present invention are produced from one or more types of conventionally spun fibers or filaments having, for instance, round, delta, . .trifocal.!. .Iadd.trilobal.Iaddend., or diamond cross sectional configurations.
Nonwoven cover stock of the above defined types can usefully vary in weight from about 10-45 gm yd2 or higher.
The invention is further illustrated but not limited by the following Examples and Tables:
A. Polypropylene in flake form and characterized as follows: (crystallinity 60% Mw 3.5×105, molecular weight distribution 6.4, and melt flow 3.2 g/10 minutes) is mixed in an impact blender. After thorough blending, the mixture is fed into a 11/2 extruder and spun through a 210 hole spinnerette at 280° C., air quenched, and stretched at 115° C. (4×) to obtain a 2 dpf circular filament which is then passed over a feed or kiss wheel partly immersed in a tank of first modifier composition consisting of a 50% aqueous solution of Lurol® AS-Y.sup.(*1), a neutralized phosphoric acid/alcohol ester, contact being of sufficient duration and speed to topically apply about 0.6 wt. % of the dried composition. The resulting continuous filament is crimped at about 100° C. and spray coated (0.10 wt %) with a second modifier composition consisting of a 20:1 mixture by weight of a 60% polydimethyl siloxane emulsion commercially available as LE-458HS.sup.(*2) and a 50% aqueous solution of Lurol AS-Y. After air drying, the coated 2.0 dpf fiber is chopped to 1.5" length staple and set aside for conventional ASTM Sink Time tests in which a given weight of fiber is loosely packed into a mesh basket and the sink time measured in seconds. The remainder is carded into webs weighing about 20 g/yd2, two webs being calender bonded at 162° C. to obtain test nonwoven material. The test nonwoven is cut into strips of convenient dimensions for carrying out conventional strength and run off tests using syn urine.sup.(*3) as the wetting fluid. Test results, are summarized and reported in Tables I and II.
TABLE I__________________________________________________________________________STAPLE PROPERTIESColor Degree of Percent Finish Tenacity Elongation Spin Fin. Over Fin.Sample #Type Hydrophobicity*4 MFR Tow Staple DPF gms % CPI Type/AMT Type/AMT__________________________________________________________________________S-1 195 5 17.6 0.77 0.41 2.6 2.05 308.7 28.9 263/0.6 262/0.3S-2 187 5 35.7 0.31 0.49 2.0 -- -- -- 263/0.2 262/0.3S-3 195 5 24.3 0.15 -- 2.2 263/0.2 262/0.15*5S-4 187 5 21.7 0.48 0.48 2.43 1.68 402.0 25.1 263/0.2 262/0.3Lt. BlueS-5 187 5 22.2 0.25 0.38 2.54 1.72 424.8 28.5 263/0.2 262/0.3Med. BlueS-6 195 5 21.0 0.5 0.53 2.28 1.91 375.1 26.0 263/0.4 262/0.3S-7 195 5 21.0 0.5 0.51 2.38 1.86 373.8 21.5 263/0.4 262/0.3*6S-8 195 5 21.0 0.5 0.48 2.45 2.10 411.4 22.8 263/0.4 262/0.3*7S-9 195 5 21.0 0.5 0.60 2.43 1.91 363.0 22.1 263/0.4 262/0.3*8S-10 195 5 21.0 0.5 0.61 2.50 1.93 361.5 20.5 263/0.4 262/0.3*9S-11 187 5 0.42 -- -- -- -- 30.8 263/0.4 262/0.3Lt. BlueS-12 187 5 0.45 -- -- -- -- 30.8 263/0.4 262/0.3Med. BlueS-13 195 5 22.3 0.35 0.4 2.42 1.87 273.9 27.5 263/0.4 262/0.15S-14 187 5 19.8 0.47 0.52 2.36 21.3 263/0.4 262/0.3BlueS-15 187 5 20.9 0.56 0.53 2.42 1.80 297.0 27.8 263/0.4 262/0.3Blue 225S-16 187 5 20.8 0.44 0.48 2.13 1.92 347.0 26.3 263/0.4 262/0.3Blue 275__________________________________________________________________________ *4 1 = Fully Hydrophilic 5 = Fully Hydrophobic based on Fiber Sink Test. *5 Added Finish No. 262 to tow with kim roll to reduce static. Total 262 addon not known. *6 Finish No. 262 + 0.08 Lurol ASY; *7 Extra (0.24) Lurol ASY: *8 Extra 0.32 Lurol ASY. *9 Extra 0.72 Lurol ASY
TABLE II__________________________________________________________________________THERMOBONDED WEBBond Bond Line Speed Strength g/in.*10 Elongation %*10 Run-Off Rewet Strike TimeStaple Temp. °C. Press. Pli ft./min. MD CD MD CD % gms. sec.__________________________________________________________________________S-1 165 160 250 930 271 43 86 98.3 *11 *11S-2 160 160 250 892 288 27 70 99.3 *11 *11S-3 157.5 160 100 1294 325 30 77 97.3 *11 *11S-4 160 160 250 1716 339 50 101 91.2 *11 *11S-5 155 160 100 1500 423 37 87 94.7 *11 *11S-6 155 160 100 1463 310 27 70 95.9 0.105 *11S-7 155 160 100 1345 292 27 76 95.0 0.120 *11S-8 155 160 100 1188 285 23 78 97.1 0.111 *11S-9 155 160 100 1325 255 28 70 94.1 0.102 *11S-10 155 160 100 1391 220 29 73 98.8 0.147 *11S-11 152.5 160 100 1244 257 31 71 93.0 *11 *11S-12 152.5 160 100 1389 294 37 80 95.2 *11 *11S-13 150 160 100 *12 *12 *12 *12 91.5 *11 *11S-14 157.5 160 100 1944 533 34 78 95.0 *11 *11S-15 157.5 160 -- *12 *12 *12 *12 94.9 *11 *11S-16 157.5 160 100 1347 392 26 80 >90.0 *11 *11__________________________________________________________________________ *10 20 g/yd2 Wet *11 Could not test. Solution remained on surface of fabric in Run Of Test (fully hydrophobic) *12 No determination run.
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|Clasificación de EE.UU.||156/308.8, 428/391, 442/359, 427/393.1, 252/8.81, 156/296, 428/369, 156/305, 524/274|
|Clasificación internacional||D06M13/292, D06M15/643|
|Clasificación cooperativa||Y10T442/635, Y10T428/2962, D06M13/292, D06M7/00, Y10T428/2922, D06M2200/40, D06M15/643|
|Clasificación europea||D06M7/00, D06M13/292, D06M15/643|
|9 Jul 1997||AS||Assignment|
Owner name: FIBERCO, INC., DELAWARE
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Year of fee payment: 8
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Year of fee payment: 12
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