US3454519A - Polyolefin fibers - Google Patents
Polyolefin fibers Download PDFInfo
- Publication number
- US3454519A US3454519A US450203A US3454519DA US3454519A US 3454519 A US3454519 A US 3454519A US 450203 A US450203 A US 450203A US 3454519D A US3454519D A US 3454519DA US 3454519 A US3454519 A US 3454519A
- Authority
- US
- United States
- Prior art keywords
- polypropylene
- fibers
- hosiery
- lubrication
- fiber
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000835 fiber Substances 0.000 title description 47
- 229920000098 polyolefin Polymers 0.000 title description 2
- 239000004743 Polypropylene Substances 0.000 description 53
- -1 polypropylene Polymers 0.000 description 53
- 229920001155 polypropylene Polymers 0.000 description 53
- 238000005461 lubrication Methods 0.000 description 23
- 239000004744 fabric Substances 0.000 description 18
- 239000000194 fatty acid Chemical class 0.000 description 14
- 239000000314 lubricant Substances 0.000 description 14
- 235000014113 dietary fatty acids Nutrition 0.000 description 12
- 229930195729 fatty acid Chemical class 0.000 description 12
- 150000004665 fatty acids Chemical class 0.000 description 12
- 150000001408 amides Chemical class 0.000 description 11
- 238000000034 method Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- UAUDZVJPLUQNMU-UHFFFAOYSA-N Erucasaeureamid Natural products CCCCCCCCC=CCCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-UHFFFAOYSA-N 0.000 description 10
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- 238000011282 treatment Methods 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 238000009940 knitting Methods 0.000 description 5
- 239000004753 textile Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 4
- 239000002253 acid Chemical class 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 230000001050 lubricating effect Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000012209 synthetic fiber Substances 0.000 description 3
- 229920002994 synthetic fiber Polymers 0.000 description 3
- 238000009941 weaving Methods 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- ILRSCQWREDREME-UHFFFAOYSA-N dodecanamide Chemical compound CCCCCCCCCCCC(N)=O ILRSCQWREDREME-UHFFFAOYSA-N 0.000 description 2
- 238000005108 dry cleaning Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 238000009991 scouring Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 230000002459 sustained effect Effects 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- 229920004934 Dacron® Polymers 0.000 description 1
- ORAWFNKFUWGRJG-UHFFFAOYSA-N Docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(N)=O ORAWFNKFUWGRJG-UHFFFAOYSA-N 0.000 description 1
- FATBGEAMYMYZAF-MDZDMXLPSA-N Elaidamide Chemical compound CCCCCCCC\C=C\CCCCCCCC(N)=O FATBGEAMYMYZAF-MDZDMXLPSA-N 0.000 description 1
- 239000004605 External Lubricant Substances 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- SFIHQZFZMWZOJV-UHFFFAOYSA-N Linolsaeure-amid Natural products CCCCCC=CCC=CCCCCCCCC(N)=O SFIHQZFZMWZOJV-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000002202 Polyethylene glycol Chemical class 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 238000009954 braiding Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- TUTWLYPCGCUWQI-UHFFFAOYSA-N decanamide Chemical compound CCCCCCCCCC(N)=O TUTWLYPCGCUWQI-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 229920006379 extruded polypropylene Polymers 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 238000007380 fibre production Methods 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 238000004900 laundering Methods 0.000 description 1
- 229940116335 lauramide Drugs 0.000 description 1
- 210000002414 leg Anatomy 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- SFIHQZFZMWZOJV-HZJYTTRNSA-N linoleamide Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(N)=O SFIHQZFZMWZOJV-HZJYTTRNSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- FATBGEAMYMYZAF-UHFFFAOYSA-N oleicacidamide-heptaglycolether Natural products CCCCCCCCC=CCCCCCCCC(N)=O FATBGEAMYMYZAF-UHFFFAOYSA-N 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- 229920001223 polyethylene glycol Chemical class 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229940037312 stearamide Drugs 0.000 description 1
- 239000008117 stearic acid Chemical class 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
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
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/20—Carboxylic acid amides
-
- 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
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/04—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins
- D01F6/06—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins from polypropylene
Definitions
- This invention relates to improved fibers prepared from polyolefin polymers, and more particularly to improved polypropylene fibers.
- the invention also pertains to fabrics Which are knitted or woven from yarns formed from the improved polypropylene fibers.
- fibers or filaments of polypropylene are prepared by extruding molten polypropylene or a solution of polypropylene through a die provided with numerous, downward-facing, small round openings. Such dies are known as spinnerets.
- the extruded polypropylene fibers may either be air dried or quenched. If solvent is present, it may be removed by evaporation carried out by passing the hot fiber through heated air. The solvent may also be removed by extruding the fiber into a bath which extracts or dissolves out the solvent. The fiber is then dried by the usual means.
- Subsequent processing steps include orientation or stretching, take-up and draw-twisting of the fibers. More specifically, the fibers may be stretched and then knitted or woven as monofilament or multifilament yarn to manufacture various fabrics and finished articles such as hosiery. In many instances, the fibers are formed into yarns of the desired denier by twisting and doubling operations prior to being knitted or woven. It is also possible to combine the polypropylene fibers with other material or synthetic fibers to form different types of yarns.
- polypropylene is intended to mean normally solid, linear polymers of propylene.
- the preferred polypropylene polymers for the purposes of this invention are composed predominately of isotactic polypropylene.
- Some atactic polypropylene may be present, and broadly may constitute up to 20% or higher by weight of the polypropylene.
- the polypropylene will contain less than about 8% by weight of the atactic form of polypropylene.
- the polypropylene will generally have an intrinsic viscosity of about 0.3 to 2 or higher.
- lubricants and lubricating compositions have been employed heretofore in the spin finishing and other surface lubricating treatments as described above.
- Such lubricants have included, for example, mineral oils, mineral oil emulsions, ethoxylated fatty alcohols and acids, stearic acid and other fatty acids, polyethylene glycol esters, waxes, and the like.
- lubricants such as mineral oils or emulsion thereof cannot be employed, since they are readily absorbed by the polypropylene fibers, and cause swelling thereof.
- One object of the present invention is to avoid the difficulties encountered in the prior art with respect to furnishing surface lubrication to polypropylene fibers and to finished articles fabricated therefrom.
- Another object of the present invention is to provide improved polypropylene fibers or filaments which do not require the reapplication of surface lubrication.
- a further object of the present invention is to provide fabrics or finished articles from polypropylene fibers characterized by having outstanding surface lubrication which is not readily depletable.
- amide of a higher fatty acid is intended to apply to amides of saturated and unsaturated monocarboxylic acids, and particularly those having from 10 to 22 carbon atoms, preferably 16 to 22 carbon atoms, per molecule. Such acids are found as free acids or their glycerides in fatty oils.
- Suitable amides for the present purposes include lauramide, stearamide, oleamide, erucamide, elaidamide, linoleamide behenamide, palmitamide, N,N -ethylene-bis-oleamide, decanamide, and the like as well as mixtures thereof. It will be understood that commercially available amides or amide mixtures may be eifectively employed in the present invention.
- the amount of fatty acid amide employed in conjunction with the polypropylene may vary over a rather wide range. In general, however, the amount of fatty acid amide employed will range from about 0.01 to 1% by weight, based on the weight of the polypropylene. Preferably about 0.01 to 0.3% by weight of the fatty acid amide is utilized to achieve the desired results.
- polypropylene consisting predominantly of isotatic polypropylene
- similar or related polymers or polymer components may also be used as the starting material.
- Such other polymeric materials include copolymers of polypropylene, mixtures of polypropylene and other polymers, mixed polymers of polypropylene, as well as poly(4-methyl)pentene polymers.
- the polypropylene-fatty acid amide compositions may be prepared by any method for obtaining a uniform mixture for extrusion into the polypropylene filaments. This can be accomplished by the use of such methods as the addition of the amide as a solid, in solution in an inert solvent, or as a slurry in water or other media which are nonsolvent to the polypropylene, which may be in the form of pellets, dry fluff or molding powder. The resulting admixture is then dried and tumbled.
- the fatty acid amide can also be incorporated into the polypropylene either during polymerization or subsequently thereto such as by melt blending in any conventional equipment employed for polymer compounding such as a Banbury mixer, intensive mixers, Henschel mixers, plasticators, and the like. It is also possible to prepare a concentrate of the amide in the polypropylene by one of the aforedescribed methods, and then blend the concentrate with polypropylene pellets, dry fluff or molding powder by tumbling, Banbury mixing, or other suitable means. It is also possible to have certain conventional additives such as antioxidants, heat and light stabilizers, antistatic compounds, dyes, pigments and the like present in the polypropylene feed resin.
- the dispersion of the fatty acid amide in the polypropylene has been found to result in a sustained lubrication of the polypropylene fiber or filament surface.
- the fatty acid amides appear to be somewhat incompatible with the polypropylene and, consequently, there is a substantially continuous exudation or sweating-out of the amide from the internal or inner portion to the surface of the polypropylene filament or fiber.
- the presence of the fatty acid amide in the interior part of the filament is somewhat analogous to an internal reservoir which supplies a substantially continuous flow of lubricant to the surface and thereby provides a self-replenishing surface lubricant.
- fatty acid amides as described above, eliminates the majority of the subsequent external lubrication treatments as well as the requirement that the place of application be carefully selected in order to avoid a prolonged absence of surface lubrication at any point in the process of converting the raw fiber into finished fabric.
- surface lubrication of the fibers is also important even after garments or other finished articles have been fabricated therefrom.
- the lubrication permits free motion of the yarn in the fabricated articles which increases the ease in recovery to the original dimensions.
- the enhanced lubrication of the fiber surface resulting from the practice of this invention minimizes excessive heat generation during the sewing operation and at the same time minimizes the problems caused when the needle is caught on the fiber surface.
- the improved polypropylene fibers of this invention will not be deprived of their lubricity simply by subjecting the fabricated garment to a limited number of dry cleaning treatments or washings.
- EXAMPLE I Run A approximately 0.1% by weight of erucamide was blended with polypropylene resin having an isotactic content of 95.5% and then compounded with color pigments. The resulting blend was extruded in conventional melt extrusion equipment to form 15 denier monofilament and 40 denier multifilament yarns. The conventional step of orienting the yarns was accomplished using standard drawing equipment.
- Run B The same procedure of Run A was employed with the exception that no erucamide was blended into the polypropylene resin.
- EXAMPLE II A first set of several dozen womens seamless hosiery were knit on a 400 single needle knitting machine. A l5-l-0.25 Z turns polypropylene yarn was used for the leg fabric, while a 4010-0.5 S turns yarn was used for welt fabric as Well as for the heel and toe fabric. Both of these yarns were extruded from a mass colored polymer containing 0.1% by weight erucamide, as described in Run A of Example I. After knitting, the hosiery was looped and preboarded using conventional equipment and procedures. The hosiery thus produced was not washed or scoured in any manner.
- a second set of several dozen womens seamless hosiery was prepared as described above except that after preboarding the hosiery was scoured using conventional equipment and procedures.
- a third set of several dozen womens seamless hosiery was also knit as described above except that the polypropylene resin used to extrude the yarn contained no erucamide (Run B of Example I).
- the resulting hosiery was looped and preboarded using conventional equipment and procedures.
- the hosiery was then scoured, and lubricant finishes were applied in accordancewith conventional practice.
- Lubricant A is a complex amine-fatty acid derivative admixed with lanolin;
- Lubricant B is a resin wax emulsion. Both of these compositions are commercially available and in common use for hosiery finishing.
- the welt, shadow welt and knee portion of the boot are then repeatedly distended from a circumference of 12.5 inches to 22.5 inches.
- the hosiery was flexed until failure occurred.
- 1500 cycles is considered satisfactory stretch-
- the hosiery knitted from the yarns containing erucamide continued to show the same remarkable increase in flex lifedemonstrated above.
- hosiery prepared by practicing the present invention results in average flexural values which far exceed the 1500 minimum established in this field. Since convention lubrication treatments did not result in hosiery meeting the minimum values, the importance of the present invention is readily apparent. Equally satisfactory results were obtained with full fashioned womens hosiery.
- the improved polypropylene fibers and filaments of this invention may be employed to produce a wide variety of difierent types of fabrics, including both apparel and industrial textile products. Specific examples of these products include hosiery, lingerie, suitings, shirtin-gs, dress and blouse fabrics, and the like.
- the finished fabrics or articles e.g., hosiery, entirely from polypropylene fibers, mixtures of polypropylene fibers with other natural or synthetic fibers.
- the natural fibers include silk, wool and cotton; whereas the other synthetic fibers include nylon, Dacron, Acrilan, etc.
- An improved textile fiber prepared from isotactic polypropylene resin containing about 0.01 to 1.0% by weight of erucamide, said fiber being characterized by having self-replenishing surface lubrication.
- a textile fabric comprised of improved polypropylene fibers provided with sustained surface lubrication, said fibers being prepared from isotactic polypropylene resin having dispersed therein from about 0.01 to 1.0% by weight of erucamide.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Artificial Filaments (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
United States Patent US. Cl. 26032.6 3 Claims ABSTRACT OF THE DISCLOSURE Improved textile fibers prepared from isotactic polypropylene resin containing from about 0.01 to about 1.0% by weight of erucamide. These fibers and fabrics prepared therefrom are characterized by having self-replenishing surface lubrication.
This invention relates to improved fibers prepared from polyolefin polymers, and more particularly to improved polypropylene fibers. The invention also pertains to fabrics Which are knitted or woven from yarns formed from the improved polypropylene fibers.
In general, fibers or filaments of polypropylene are prepared by extruding molten polypropylene or a solution of polypropylene through a die provided with numerous, downward-facing, small round openings. Such dies are known as spinnerets. The extruded polypropylene fibers may either be air dried or quenched. If solvent is present, it may be removed by evaporation carried out by passing the hot fiber through heated air. The solvent may also be removed by extruding the fiber into a bath which extracts or dissolves out the solvent. The fiber is then dried by the usual means.
Subsequent processing steps include orientation or stretching, take-up and draw-twisting of the fibers. More specifically, the fibers may be stretched and then knitted or woven as monofilament or multifilament yarn to manufacture various fabrics and finished articles such as hosiery. In many instances, the fibers are formed into yarns of the desired denier by twisting and doubling operations prior to being knitted or woven. It is also possible to combine the polypropylene fibers with other material or synthetic fibers to form different types of yarns.
The terms fiber and filaments as set forth throughout this specification and in the appended claims will be used interchangeably in their usual and acepted sense in the textile industry. It will be further understood that the term polypropylene is intended to mean normally solid, linear polymers of propylene. As described above, the preferred polypropylene polymers for the purposes of this invention are composed predominately of isotactic polypropylene. Some atactic polypropylene may be present, and broadly may constitute up to 20% or higher by weight of the polypropylene. In the preferred practice of the present invention, the polypropylene will contain less than about 8% by weight of the atactic form of polypropylene. The polypropylene will generally have an intrinsic viscosity of about 0.3 to 2 or higher.
As is well known in this art, synthetic polymer fibers as well as natural fiber surfaces are treated with lubricants during the yarn manufacturing operation as well as during the subsequent processing steps of knitting, weaving, braiding, and the like. Surface lubrication is also performed on the knitted, Woven or braided fabrics immediately preceding their use in the manufacture of garments or other finished articles. One purpose for the application of surface lubricants is to minimize the abrasion and wear of both the fibers and the various contact points on each other during the production of the fiber.
For example, it is customary for the manufacturer of the raw fiber to apply a spin finish to the fiber during or subsequent to the spinning step. Another purpose of lubrication is to facilitate the freedom of movement of the yarn itself which may, in turn, permit easy recovery to designed, preset dimensions. Surface lubrication in the case of knitted fabrics, also permits uniform retention of stitch formation through conventional procedures such as relaxation or shrinkage, or by extended fixed dimensional settings. Related advantages are obtained with woven, nonwoven and needled fabrics. In order to accomplish such results, surface lubrication has had to be applied at various stages during the conversion of the raw fibers into finished fabrics and articles. Thus, for example, surface lubrication has been used prior to the knitting or weaving step, subsequent to knitting and weaving, subsequent to final boarding, subsequent to scouring and drying subsequent to the conventional finishing bath treatment, etc.
Conventional lubricants and lubricating compositions have been employed heretofore in the spin finishing and other surface lubricating treatments as described above. Such lubricants have included, for example, mineral oils, mineral oil emulsions, ethoxylated fatty alcohols and acids, stearic acid and other fatty acids, polyethylene glycol esters, waxes, and the like.
A number of serious difiiculties have been encountered with respect to the use and application of the conventional lubricants to the surface of polypropylene fibers. To begin with, lubricants such as mineral oils or emulsion thereof cannot be employed, since they are readily absorbed by the polypropylene fibers, and cause swelling thereof. The use of one or more of the other lubricants, on the other hand, at best only serve as transitory assistance for accomplishing the lubrication objectives sought in any of the above-mentioned steps, since they are readily removed by simple washing, scouring or dry cleaning operations. This lack of durability necessitates multiple reapplications of the surface lubricant throughout the many .and varied steps required to form the yarn and then to transform the raw yarn into finished fabrics or garments. The need for multiple reapplications of the lubricant is a serious economic disadvantage as well as a source of trouble during the formation of the yarn and the fabrication of finished articles therefrom.
One object of the present invention is to avoid the difficulties encountered in the prior art with respect to furnishing surface lubrication to polypropylene fibers and to finished articles fabricated therefrom.
Another object of the present invention is to provide improved polypropylene fibers or filaments which do not require the reapplication of surface lubrication.
A further object of the present invention is to provide fabrics or finished articles from polypropylene fibers characterized by having outstanding surface lubrication which is not readily depletable.
These and other objects of the present invention will become apparent from the ensuing description and illustrative embodiments.
In accordance with the present invention it has now been found that durable, self-replenishing, surface lubricity can be imparted to a polypropylene fiber or filament by incorporating an amide or a mixture of amides of higher fatty acids into the polypropylene resin feed material. The term amide of a higher fatty acid is intended to apply to amides of saturated and unsaturated monocarboxylic acids, and particularly those having from 10 to 22 carbon atoms, preferably 16 to 22 carbon atoms, per molecule. Such acids are found as free acids or their glycerides in fatty oils. Examples of suitable amides for the present purposes include lauramide, stearamide, oleamide, erucamide, elaidamide, linoleamide behenamide, palmitamide, N,N -ethylene-bis-oleamide, decanamide, and the like as well as mixtures thereof. It will be understood that commercially available amides or amide mixtures may be eifectively employed in the present invention.
The amount of fatty acid amide employed in conjunction with the polypropylene may vary over a rather wide range. In general, however, the amount of fatty acid amide employed will range from about 0.01 to 1% by weight, based on the weight of the polypropylene. Preferably about 0.01 to 0.3% by weight of the fatty acid amide is utilized to achieve the desired results.
Although the present invention has been discussed above and will be illustrated below in connection with polypropylene consisting predominantly of isotatic polypropylene, it will be understood that similar or related polymers or polymer components may also be used as the starting material. Such other polymeric materials include copolymers of polypropylene, mixtures of polypropylene and other polymers, mixed polymers of polypropylene, as well as poly(4-methyl)pentene polymers.
The polypropylene-fatty acid amide compositions may be prepared by any method for obtaining a uniform mixture for extrusion into the polypropylene filaments. This can be accomplished by the use of such methods as the addition of the amide as a solid, in solution in an inert solvent, or as a slurry in water or other media which are nonsolvent to the polypropylene, which may be in the form of pellets, dry fluff or molding powder. The resulting admixture is then dried and tumbled. The fatty acid amide can also be incorporated into the polypropylene either during polymerization or subsequently thereto such as by melt blending in any conventional equipment employed for polymer compounding such as a Banbury mixer, intensive mixers, Henschel mixers, plasticators, and the like. It is also possible to prepare a concentrate of the amide in the polypropylene by one of the aforedescribed methods, and then blend the concentrate with polypropylene pellets, dry fluff or molding powder by tumbling, Banbury mixing, or other suitable means. It is also possible to have certain conventional additives such as antioxidants, heat and light stabilizers, antistatic compounds, dyes, pigments and the like present in the polypropylene feed resin.
The dispersion of the fatty acid amide in the polypropylene has been found to result in a sustained lubrication of the polypropylene fiber or filament surface. The fatty acid amides appear to be somewhat incompatible with the polypropylene and, consequently, there is a substantially continuous exudation or sweating-out of the amide from the internal or inner portion to the surface of the polypropylene filament or fiber. The presence of the fatty acid amide in the interior part of the filament is somewhat analogous to an internal reservoir which supplies a substantially continuous flow of lubricant to the surface and thereby provides a self-replenishing surface lubricant.
It was further found that when amides are incorporated in the polypropylene the lubricity of the filament or fiber surface is maintained over a comparatively long period of time. Consequently, the multiplicity of external surface lubricating treatments heretofore required could be eliminated without encountering any untoward results. Various problems which have developed from time to time in fiber production and in the manufacture of fabrics therefrom as a result of insufficient or nondurable surface lubrication were avoided. The use of the fatty acid amides also resulted in overall economic advantages over the prior art lubrication procedures. Although all or substantially all of the previous external lubrication treatment steps could be omitted by the practice of this invention, in some instances the application of an external lubricant is maintained. The use of the fatty acid amides, as described above, eliminates the majority of the subsequent external lubrication treatments as well as the requirement that the place of application be carefully selected in order to avoid a prolonged absence of surface lubrication at any point in the process of converting the raw fiber into finished fabric.
As previously mentioned, surface lubrication of the fibers is also important even after garments or other finished articles have been fabricated therefrom. The lubrication permits free motion of the yarn in the fabricated articles which increases the ease in recovery to the original dimensions. Furthermore, it should be noted that the enhanced lubrication of the fiber surface resulting from the practice of this invention minimizes excessive heat generation during the sewing operation and at the same time minimizes the problems caused when the needle is caught on the fiber surface. Finally, the improved polypropylene fibers of this invention will not be deprived of their lubricity simply by subjecting the fabricated garment to a limited number of dry cleaning treatments or washings.
The invention will be more fully understood by reference to the following illustrative embodiments.
EXAMPLE I Run A.Approximately 0.1% by weight of erucamide was blended with polypropylene resin having an isotactic content of 95.5% and then compounded with color pigments. The resulting blend was extruded in conventional melt extrusion equipment to form 15 denier monofilament and 40 denier multifilament yarns. The conventional step of orienting the yarns was accomplished using standard drawing equipment.
Run B.The same procedure of Run A was employed with the exception that no erucamide was blended into the polypropylene resin.
EXAMPLE II A first set of several dozen womens seamless hosiery were knit on a 400 single needle knitting machine. A l5-l-0.25 Z turns polypropylene yarn was used for the leg fabric, while a 4010-0.5 S turns yarn was used for welt fabric as Well as for the heel and toe fabric. Both of these yarns were extruded from a mass colored polymer containing 0.1% by weight erucamide, as described in Run A of Example I. After knitting, the hosiery was looped and preboarded using conventional equipment and procedures. The hosiery thus produced was not washed or scoured in any manner.
A second set of several dozen womens seamless hosiery was prepared as described above except that after preboarding the hosiery was scoured using conventional equipment and procedures.
A third set of several dozen womens seamless hosiery was also knit as described above except that the polypropylene resin used to extrude the yarn contained no erucamide (Run B of Example I). The resulting hosiery was looped and preboarded using conventional equipment and procedures. The hosiery was then scoured, and lubricant finishes were applied in accordancewith conventional practice. Lubricant A is a complex amine-fatty acid derivative admixed with lanolin; Lubricant B is a resin wax emulsion. Both of these compositions are commercially available and in common use for hosiery finishing.
The above described three sets of hosiery were tested to determine stretch-endurability on the Frazier Hosiery Testing Machine utilizing the present improved model of the machine originally built for the National Bureau of Standards. This is the standard test in the field, and the machine as well as the exact method employed are described in deteail by Schiefer et al., US. Bureau of Standards Journal of Research, 12, No. 5, pp. 54349, Research Paper RP 679 (1934). In this test the hosiery is first Washed by hand and air dried. The hosiery is then placed on the machine at a length between the heel and garter clasp governed by the overall flat measurement of the hose. The welt, shadow welt and knee portion of the boot are then repeatedly distended from a circumference of 12.5 inches to 22.5 inches. The hosiery was flexed until failure occurred. In accordance with the established standard, 1500 cycles is considered satisfactory stretch- On repeated launderings both in laboratory and in wear tests, the hosiery knitted from the yarns containing erucamide continued to show the same remarkable increase in flex lifedemonstrated above.
The above data show that the average number of fiexures for the hosiery prepared from fibers of the erucamide containing polypropylene resin was considerably higher than that obtained by use of the conventional external application of surface lubrication. Moreover, the
hosiery prepared by practicing the present invention results in average flexural values which far exceed the 1500 minimum established in this field. Since convention lubrication treatments did not result in hosiery meeting the minimum values, the importance of the present invention is readily apparent. Equally satisfactory results were obtained with full fashioned womens hosiery.
The improved polypropylene fibers and filaments of this invention may be employed to produce a wide variety of difierent types of fabrics, including both apparel and industrial textile products. Specific examples of these products include hosiery, lingerie, suitings, shirtin-gs, dress and blouse fabrics, and the like.
Although it is preferred to fabricate the finished fabrics or articles, e.g., hosiery, entirely from polypropylene fibers, mixtures of polypropylene fibers with other natural or synthetic fibers. The natural fibers include silk, wool and cotton; whereas the other synthetic fibers include nylon, Dacron, Acrilan, etc.
While particular embodiments of the present invention have been shown above, it will be understood that the invention is obviously subject to variations and modifications without departing from its broadest aspects.
We claim:
1. An improved textile fiber prepared from isotactic polypropylene resin containing about 0.01 to 1.0% by weight of erucamide, said fiber being characterized by having self-replenishing surface lubrication.
2. A textile fabric comprised of improved polypropylene fibers provided with sustained surface lubrication, said fibers being prepared from isotactic polypropylene resin having dispersed therein from about 0.01 to 1.0% by weight of erucamide.
3. A stocking prepared from the improved polypropylene fibers of claim 1.
References Cited UNITED STATES PATENTS 2,938,879 5/1960 Mock et al. 3,107,228 10/1963 Cappuccio et al. 3,141,872 7/1964 Natta et a1. 260-93.7 3,176,021 3/ 1965 Volungis et al.
FOREIGN PATENTS 867,280 5/1961 Great Britain.
ALLAN LIEBERMAN, Primary Examiner.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45020365A | 1965-04-22 | 1965-04-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3454519A true US3454519A (en) | 1969-07-08 |
Family
ID=23787190
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US450203A Expired - Lifetime US3454519A (en) | 1965-04-22 | 1965-04-22 | Polyolefin fibers |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3454519A (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0400622A3 (en) * | 1989-06-01 | 1991-09-11 | Hercules Incorporated | Rewettable polyolefin fiber and corresponding nonwovens |
| US20030049989A1 (en) * | 2001-08-07 | 2003-03-13 | Richard Ferencz | Thermoplastic constructs with improved softness |
| US20030157859A1 (en) * | 2000-02-10 | 2003-08-21 | Masahide Ishikawa | Nonwoven fabric, process for producing the same, sanitary material and sanitary supply |
| US20030181112A1 (en) * | 2000-06-13 | 2003-09-25 | Masahide Ishikawa | Spunbonded nonwoven fabric and absorbent article |
| US20040005457A1 (en) * | 2002-07-03 | 2004-01-08 | Kimberly-Clark Worldwide, Inc. | Methods of improving the softness of fibers and nonwoven webs and fibers and nonwoven webs having improved softness |
| US20040058610A1 (en) * | 2000-09-18 | 2004-03-25 | Masahide Ishikawa | Multilayer non-woven fabric and use thereof |
| US6740609B1 (en) | 2000-08-15 | 2004-05-25 | Polymer Group, Inc. | Soft polypropylene melt spun nonwoven fabric |
| WO2007140163A3 (en) * | 2006-05-25 | 2008-04-24 | Dow Global Technologies Inc | Soft and extensible polypropylene based spunbond nonwovens |
| EP1138472B2 (en) † | 2000-03-30 | 2012-10-03 | Uni-Charm Corporation | Elastically stretchable composite sheet and process for making the same |
| EP3372212A1 (en) | 2017-03-09 | 2018-09-12 | The Procter and Gamble Company | Absorbent core wrap with a low basis weight nonwoven in the bottom layer |
| US10870936B2 (en) | 2013-11-20 | 2020-12-22 | Kimberly-Clark Worldwide, Inc. | Soft and durable nonwoven composite |
| US10946117B2 (en) | 2013-11-20 | 2021-03-16 | Kimberly-Clark Worldwide, Inc. | Absorbent article containing a soft and durable backsheet |
| US20240115432A1 (en) * | 2021-06-30 | 2024-04-11 | Asahi Kasei Kabushiki Kaisha | Nonwoven Fabric, Use of Same, and Method for Producing Nonwoven Fabric |
| EP4461279A1 (en) | 2023-05-11 | 2024-11-13 | The Procter & Gamble Company | Absorbent article comprising a carded calendered nonwoven |
| WO2024229791A1 (en) | 2023-05-11 | 2024-11-14 | The Procter & Gamble Company | Carded calendered nonwovens |
| WO2024229793A1 (en) | 2023-05-11 | 2024-11-14 | The Procter & Gamble Company | Absorbent article comprising a carded calendered nonwoven |
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| GB867280A (en) * | 1957-06-28 | 1961-05-03 | Union Carbide Corp | Non-blocking polymeric mono-olefine compositions |
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| US2938879A (en) * | 1955-10-18 | 1960-05-31 | Union Carbide Corp | Non-blocking polyethylene compositions |
| US3107228A (en) * | 1956-12-12 | 1963-10-15 | Montecatimi Societa Generale P | Polypropylene containing a dye-receptive modifier which comprises polyal-kyleneimine or mixztures thereof with an epoxy resin |
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Cited By (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5582904A (en) * | 1989-06-01 | 1996-12-10 | Hercules Incorporated | Rewettable polyolefin fiber and corresponding nonwovens |
| EP0400622A3 (en) * | 1989-06-01 | 1991-09-11 | Hercules Incorporated | Rewettable polyolefin fiber and corresponding nonwovens |
| US20030157859A1 (en) * | 2000-02-10 | 2003-08-21 | Masahide Ishikawa | Nonwoven fabric, process for producing the same, sanitary material and sanitary supply |
| EP1275763A4 (en) * | 2000-02-10 | 2005-09-21 | Idemitsu Unitech Co Ltd | LIQUID, MANUFACTURING METHOD, HYGIENIC MATERIALS AND HYGIENE ITEMS |
| EP1138472B2 (en) † | 2000-03-30 | 2012-10-03 | Uni-Charm Corporation | Elastically stretchable composite sheet and process for making the same |
| US20030181112A1 (en) * | 2000-06-13 | 2003-09-25 | Masahide Ishikawa | Spunbonded nonwoven fabric and absorbent article |
| AU782574B2 (en) * | 2000-08-15 | 2005-08-11 | Polymer Group, Inc. | Soft polypropylene melt spun nonwoven fabric |
| US6740609B1 (en) | 2000-08-15 | 2004-05-25 | Polymer Group, Inc. | Soft polypropylene melt spun nonwoven fabric |
| US20040058610A1 (en) * | 2000-09-18 | 2004-03-25 | Masahide Ishikawa | Multilayer non-woven fabric and use thereof |
| US7238313B2 (en) * | 2001-08-07 | 2007-07-03 | Polymer Group, Inc. | Thermoplastic constructs with improved softness |
| US20030049989A1 (en) * | 2001-08-07 | 2003-03-13 | Richard Ferencz | Thermoplastic constructs with improved softness |
| WO2004005601A1 (en) * | 2002-07-03 | 2004-01-15 | Kimberly-Clark Worldwide, Inc. | Methods of improving the softness of fibers and nonwoven webs and fibers and nonwoven webs havinb improved softness |
| US20040005457A1 (en) * | 2002-07-03 | 2004-01-08 | Kimberly-Clark Worldwide, Inc. | Methods of improving the softness of fibers and nonwoven webs and fibers and nonwoven webs having improved softness |
| WO2007140163A3 (en) * | 2006-05-25 | 2008-04-24 | Dow Global Technologies Inc | Soft and extensible polypropylene based spunbond nonwovens |
| US20090111347A1 (en) * | 2006-05-25 | 2009-04-30 | Hong Peng | Soft and extensible polypropylene based spunbond nonwovens |
| US10870936B2 (en) | 2013-11-20 | 2020-12-22 | Kimberly-Clark Worldwide, Inc. | Soft and durable nonwoven composite |
| US10946117B2 (en) | 2013-11-20 | 2021-03-16 | Kimberly-Clark Worldwide, Inc. | Absorbent article containing a soft and durable backsheet |
| EP3372212A1 (en) | 2017-03-09 | 2018-09-12 | The Procter and Gamble Company | Absorbent core wrap with a low basis weight nonwoven in the bottom layer |
| WO2018164875A1 (en) | 2017-03-09 | 2018-09-13 | The Procter & Gamble Company | Absorbent core wrap with a low basis weight nonwoven in the bottom layer |
| US20240115432A1 (en) * | 2021-06-30 | 2024-04-11 | Asahi Kasei Kabushiki Kaisha | Nonwoven Fabric, Use of Same, and Method for Producing Nonwoven Fabric |
| US12207997B2 (en) * | 2021-06-30 | 2025-01-28 | Mitsui Chemicals Asahi Life Materials Co., Ltd. | Nonwoven fabric, use of same, and method for producing nonwoven fabric |
| EP4461279A1 (en) | 2023-05-11 | 2024-11-13 | The Procter & Gamble Company | Absorbent article comprising a carded calendered nonwoven |
| EP4461858A1 (en) | 2023-05-11 | 2024-11-13 | The Procter & Gamble Company | Carded calendered nonwovens |
| WO2024229791A1 (en) | 2023-05-11 | 2024-11-14 | The Procter & Gamble Company | Carded calendered nonwovens |
| WO2024229793A1 (en) | 2023-05-11 | 2024-11-14 | The Procter & Gamble Company | Absorbent article comprising a carded calendered nonwoven |
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