US3379001A - Blends of cellulosic and polypivalolactone staple fibers - Google Patents
Blends of cellulosic and polypivalolactone staple fibers Download PDFInfo
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- US3379001A US3379001A US447081A US44708165A US3379001A US 3379001 A US3379001 A US 3379001A US 447081 A US447081 A US 447081A US 44708165 A US44708165 A US 44708165A US 3379001 A US3379001 A US 3379001A
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- US
- United States
- Prior art keywords
- fibers
- polypivalolactone
- blends
- staple
- cellulosic
- Prior art date
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- 238000011084 recovery Methods 0.000 description 32
- 229920000297 Rayon Polymers 0.000 description 24
- 239000002964 rayon Substances 0.000 description 22
- -1 polyethylene terephthalate Polymers 0.000 description 16
- 229920000139 polyethylene terephthalate Polymers 0.000 description 14
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- 238000012360 testing method Methods 0.000 description 12
- 239000008188 pellet Substances 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 9
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- 206010040954 Skin wrinkling Diseases 0.000 description 6
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- 229920000728 polyester Polymers 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
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- TWNIBLMWSKIRAT-VFUOTHLCSA-N levoglucosan Chemical group O[C@@H]1[C@@H](O)[C@H](O)[C@H]2CO[C@@H]1O2 TWNIBLMWSKIRAT-VFUOTHLCSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000009987 spinning Methods 0.000 description 3
- ULKFLOVGORAZDI-UHFFFAOYSA-N 3,3-dimethyloxetan-2-one Chemical compound CC1(C)COC1=O ULKFLOVGORAZDI-UHFFFAOYSA-N 0.000 description 2
- RDFQSFOGKVZWKF-UHFFFAOYSA-N 3-hydroxy-2,2-dimethylpropanoic acid Chemical compound OCC(C)(C)C(O)=O RDFQSFOGKVZWKF-UHFFFAOYSA-N 0.000 description 2
- 229920013682 Avisco Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
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- 239000004408 titanium dioxide Substances 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- YGMFEPNXMQXUBH-UHFFFAOYSA-N 3,3-bis(chloromethyl)oxetan-2-one Chemical compound ClCC1(CCl)COC1=O YGMFEPNXMQXUBH-UHFFFAOYSA-N 0.000 description 1
- FQFQWTFNRFUWKM-UHFFFAOYSA-N 3,3-diethyloxetan-2-one Chemical compound CCC1(CC)COC1=O FQFQWTFNRFUWKM-UHFFFAOYSA-N 0.000 description 1
- 241001086826 Branta bernicla Species 0.000 description 1
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- 239000004677 Nylon Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 1
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- 238000009940 knitting Methods 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
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- 229910052751 metal Inorganic materials 0.000 description 1
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- 238000012986 modification Methods 0.000 description 1
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- 229920001778 nylon Polymers 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
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- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
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- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- UKLNMMHNWFDKNT-UHFFFAOYSA-M sodium chlorite Chemical compound [Na+].[O-]Cl=O UKLNMMHNWFDKNT-UHFFFAOYSA-M 0.000 description 1
- 229960002218 sodium chlorite Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
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- 230000002269 spontaneous effect Effects 0.000 description 1
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- 239000012815 thermoplastic material Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 210000000689 upper leg Anatomy 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
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Classifications
-
- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/02—Yarns or threads characterised by the material or by the materials from which they are made
- D02G3/04—Blended or other yarns or threads containing components made from different materials
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2904—Staple length fiber
Definitions
- This invention relates to novel cellulosic fiber blends.
- Cellulosic fibers such as cotton and rayon are abundant and inexpensive, and they are useful for making a wide variety of articles. Garments made from them are considered comfortable and aesthetically pleasing when properly cared for.
- cellulosic fibers are known to have poor recovery properties, such as inferior recovery from compression and poor ability to recover from wrinkling in fabric form.
- Such deficiencies have imposed limitations on the use of cellulosic fibers for certain forms of stuffing materials, for high performance wash-wear garments requiring only minimum care, and for carpets and other articles requiring good recovery properties.
- Blends of cellulosic fibers with as little as 5% of polypivalolactone staple fibers exhibits markedly improved recovery properties.
- Blends of cellulosic fibers with at least about polypivalolactone staple fibers give striking results; such blends have higher recovery from compression, and fabrics made of the blends have better wash-wear performance, than cellulosic fiber blends containing 65% polyethylene terephthalate fiber, Even more outstanding results are obtained with blends containing about equal parts of cellulosic fibers and polypivalolactone fibers. Still higher proportions of the polypivalolactone may be used if desired, of course.
- the cellulosic fiber blends of this invention are particularly well adapted for the preparation of staple yarns to be used in making fabrics for wash-wear garments.
- Great efforts have been expended on the development of such garments, requiring only minimum care.
- the goal has been a garment which presents and retains a neat appearance during wearing, without the development of Wrinkles; and which can then be laundered in hot water, dried on the line, and still present a neat appearance when worn again without the necessity of pressing to remove wrinkles.
- Blends containing about 35% cotton and 65 polyethylene terephthalate fiber have achieved commercial importance, since they provide considerable improvement over 100% cotton fabrics in wash-wear performance.
- garments made from blends of cotton with from about 15% to about 50% polypivalolactone staple fiber exhibit superior wash-wear performance and also have high aesthetic appeal because they contain such a high proportion of cotton.
- blends containing up to 80% polypivalolactone fiber with cellulosic fiber may be employed. It is preferred, however, that the blends contain at least about cellulosic fiber when 3,379,001 Patented Apr. 23, 1%68 ice it is desired to incorporate in the fabric to a considerable extent the aesthetics of cellulosic fibers.
- any of the various conventional methods for mixing the cellulosic fibers with fibers of synthetic polymers to form a blend and working up the fiber blend to form a fabric may be employed, Standard textile equipment may be used for processing cellulosic staple blends into staple yarns, and weaving or knitting the yarns into fabrics.
- Standard textile equipment may be used for processing cellulosic staple blends into staple yarns, and weaving or knitting the yarns into fabrics.
- the properties and performance of a fabric are dependent upon its construction; but for any given fabric construction, the novel cellulosic fiber/polypivalolactone staple fiber blends of the invention yield markedly superior results to those obtained with cellulosic fibers used alone.
- cellulosic fiber refers to any fiber composed substantially of cellulose. Included are both natural cellulosic fibers such as cotton, fiax, hemp, etc. and rayon, or other fibers of regenerated cellulose, whether linear or cross-linked. More specifically, the term cellulose is defined as a polymer composed of anhydroglucose units linked at the 1 and 4 positions through glucosidic bonds with the beta configuration, wherein fewer than one-half of the anhydroglucose units are chemically substituted. Thus, the term does not comprehend cellulose acetate or other derivatives of cellulose in which one or more hydroxyl groups on most or all of the anhydroglucose units are esterified.
- plypivalolactone refers to a linear condensation polyester comprised essentially of recurring ester structural units of the formula
- Alternative names for the polyester include poly(hydroxypivalic acid), poly (2,2-dirnethylhydracrylic acid), and poly(oxycarbonyl-l, l-dimethyldimethylene).
- the polyester is readily prepared by the polymerization of hydroxypivalic acid or its esters as disclosed by Alderson in his US. Patent 2,658,055; or by the polymerization of pivalolactone, the intramolecular ester of hydroxypivalic acid, as disclosed by Reynolds and Vickers in their British Patent 766,347. In a typical procedure, 25 g.
- pivalolactone is added to a refluxing mixture of 250 ml. of n-h-exane, 2.5 ml. of ethyl alcohol, 0.25 g. of triethylenediamine, 0.025 g. of 2,2-bis(4-hydroxyphenyl) propane and 0.075 g. of finely divided TiO Refiuxing is continued, with stirring, for 4 hours, during which time the delustered polypivalolactone polymer precipitates from the boiling mixture. The solid polymer is subsequently separated by filtration from the hexane solvent. Minor modifications of the polypivalolactone with copolyrneric components are also comprehended.
- 2,2-diethylpropiolactone, 2,2-bis(chloromethyl)propiolactone, or other lactones or hydroxyacids may be employed as copolymeric modifiers in amounts ranging up to about 25 mol percent, preferably 1 to about 10 mol percent; or various thermoplastic materials such as other polyesters or polyamides may be incorporated in the molten polypivalolactone in amounts up to about 10% by weight.
- the polypivalolactone fiber blended with the cellulosic fiber should be oriented and possess a high degree of polymerization as characterized by an inherent viscosity of at least about 0.75, measured at 30 C. in solution in trifiuoroacetic acid at a concentration of 0.5 gram of polymer per ml. of solution.
- the polypivalolactone fibers are formed from the polymer by conventional melt-spinning techniques, usually at a spinning temperature in the range of about 250-290 C., with extrusion of the polypivalolactone filaments through capillary orifices in a spinneret and quenching with a current of air or other inert gas, or by passing the extruded filaments into an inert liquid such as water.
- the filaments may be oriented simply by taking them up on a forwarding roll or windup roll at a thigh spin-stretch factor, i.e.
- the filaments are drawn at a ratio of 1.1 to 5x.
- the oriented olypivalolactone filaments are usually crimped and are then cut to staple fibers of the desired length. If desired, the filaments may be set or relaxed at a temperature in the range of about 125-200" C., either before or after crimping.
- blend refers to an intimate mixture formed of loose staple fibers composed of different polymers, the fibers being intermingled in substantially random manner.
- the novel staple fiber blend of the invention may also contain staple fibers composed of polyamides, polyacrylonitrile, polyurethane, or other staple fibers so long as at least the minimum percentages of cellulosic fiber and polypivalolactone are present as described above, so that the percentages of all the staple fibers in the blend total 100%.
- Multi-component blends are contemplated. For example, excellent poplins, sharkskins, and twills may be prepared using 40% polypivalolactone staple fibers, 30% cotton, 20% rayon staple fibers, and nylon staple fibers.
- Example 1 Polypivalolactone having an inherent viscosity of 1.6 and containing 0.3 weight percent titanium dioxide is melt extruded at 276 C. from a spinneret containing orifices, each 0.009 inch (0.023 cm.) in diameter.
- the extruded filaments are passed through a vertical waterquench tube continuously fed by water maintained at 11 from a cylindrical pan surmounting the tube.
- the filaments are passed through a convergence guide and the yarn so formed is taken up by a roll at 800 y.p.m. (730 meters per min.) and is then passed to draw roll at 900 y.p.m. (822 m.p.m.) for a draw ratio of 1.12 after which the yarn is wound up.
- the drawn yarn has a denier of 65.
- the inherent viscosity of the polymer comprising the yarn is 1.5.
- the yarn is plied (30 ends) and the plied yarn is then heated by passing it twice around an 8-inch (20.3 cm.) roll heated to 175 C. and operated at a peripheral speed of 60 y.p.m. (55 m.p.m.) the contact time being 1.3 seconds.
- the plied yarn is padded with a 5% aqueous solution of anionic textile finishing agent and a tow sheet of plied yarns is formed and fed into a stufi'er box crimper and crimped (approximately 8 crimps per inch or about 3 crimps per cm.).
- the crimped tow is cut to give 1.5 inch (3.81 cm.) staple fibers.
- the filaments in the crimped tow have a tenacity of 4.7 g.p.d., an elongation of 90%, a modulus of 24 g.p.d., a work recovery of 72% at 5% elongation, and a tensile recovery of 88% at 5% elongation.
- Fiber blends are prepared comprising, respectively, 50% and 65% by weight of the olypivalolactone staple fibers and 50% and 35% by weight of combed El Paso cotton (middling grade). It is observed that 50% of the cotton fibers are 1 /8 inches (2.86 cm.) in length or longer.
- Other blends are prepared comprising 50% and 65% by weight of the olypivalolactone staple fibers and 50% and 35% by weight of standard, 1.5 denier rayon staple fibers having a cut length of 1% inches (3.97 cm.) (standard Avisco XL produced by the American Viscose Corporation as Style 2301).
- Busse compressional recovery test measures the ability of a pellet or plug of staple fibers to recover from compressional forces and is expressed in percent.
- the apparatus used in the Busse test is described in Textile Research Journal, 23, 84 (1953). The test is performed at 65% relativ humidity and at 70 F.
- a tuft of staple fibers weighing 0.3 gram is taken from a sliver or batt and placed in a metal cylinder which is 0.8 square inch in area (5.16 crn
- the tuft of staple is formed into a loose pellet by compressing it with a light wooden rod at approximately 0.2 p.s.i. (14 g./cm.
- the initial height of the loose pellet is then measured under this load.
- the wooden rod is then replaced with a steel rod and a loading force of 10,000 p.s.i. (703 kg./cm. is applied to the pellet for one minute.
- This compressed pellet of fiber is then removed from the cylinder and allowed to recover for 24 hours.
- the recovery in percent is calculated from the ratio of the recovered pellet height to the initial pellet height. Because of the removal of the rod before the final measurement, the recovery may be greater in some cases than the initial height.
- Example 2 A quantity of the crimped tow of Example 1 is heated for five hours at C., after which it is cut to give 1.5 inch (3.81 cm.) staple fibers.
- the filaments in the crimped tow have a tenacity of 3.0 g.p.d., an elongation of 92%, a modulus of 25 g.p.d., a work recovery of 84% at 5% elongation, and a tensile recovery of 94% at 5% elongation.
- a fiber blend is prepared comprising 50% by weight of the heat-set polypivalolactone staple fibers and 50% by weight of the cotton fibers employed in Example 1.
- a pellet of this staple blend subjected to the standard Busse compressional recovery test exhibits a recovery of 102%.
- Another fiber blend is prepared comprising 50% by Weight of the heat-set polypivalolactone staple fibers and 50% by weight of the rayon fibers employed in Example 1.
- a recovery value of 42% is obtained from a pellet of this staple blend subjected to the standard Busse compressional recovery test.
- Refiuifable pillows and durable carpets exhibiting good recovery from compression are prepared from the blends of cellulosic fibers with polypivalolactone fiber in the above example.
- Example 3 Fiber blends of the cotton fibers of Example 1 with varying amounts of the polypivalolactone staple fibers of Example 1 (crimped but not heat set) are prepared and subjected to the standard Busse compressional recovery test. Fiber blends of the same cotton fibers with the crimped, heat-set polypivalolacton staple fibers of Ex-' ample 2 are prepared in the same proportions and the Busse recovery values are measured. The results are shown in Table 2.
- the extruded filaments are passed through a vertical water-quench tube continuously fed by cold water from a cylindrical pan surmounting the tube.
- the filaments are passed through a convergence guide and the yarn so formed is taken up by a roll at 900 y.p.m. (823 m.p.m.).
- the resulting yarn has a denier of 39.
- the inherent viscosity of the polymer comprising the yarn is 1.58.
- the yarn is plied (30 ends) at 70 y.p.m. (64 m.p.m.) and the plied yarn is heat-set by passing it (at the same speed) over an 8-inch (20.3 cm.) roll heated to 175 0, contact of the yarn on the roll being maintained over an arc of 180.
- the plied yarn is then padded with a 5% aqueous anionic textile finishing agent, the pick-up of finishing agent on the yarn being about 1%, after which a tow sheet of 23 plied yarns is formed and fed into the stuffer box crim'per and crimped (8 crimps per inch or about 3 crimps per cm.).
- the filaments in the crimped tow have a tenacity of 3.8 g.p.d., an elongation of 59%, a modulus of 28 g.p.d., a work recovery of 69% at 5% elongation, and a tensile recovery of 86% at 5% elongation.
- the tow is skeined and cut to 1.5 inch (3.81 cm.) staple.
- the polypivalolactone staple fibers are blended in various ratios with cotton'fibers and with rayon fibers, following which yarns and fabrics are produced by conventional methods from the staple fiber blends and are compared with each other and with control yarns and fabrics.
- the cotton fibers employed in the various runs, with the exception described below, are combed peeler cotton (good middling grade). It is observed that 50% of the fibers are 1.25 inches (3.17 cm.) in length or longer.
- the rayon fibers employed in the various runs are standard, 1.5 denier rayon staple having a cut length of 1%; inches (3.97 cm.) (standard Avisco XL produced by the American Viscose Corporation as Style 2301).
- the 80% polypivalolactone fiber/20% cotton blend is made with different fiber samples than those described above.
- the extruded polypivalolactone filaments are quenched with room temperature air flowing radially inward toward the spinneret.
- the spinning speed is 500 y.p.m. (457 m.p.1n.), and the yarn is after-drawn 3.77 following which it is relaxed at C. for 5 minutes.
- the yarn has a spontaneous crimp of 7 crimps per inch (2.75 crimps per cm.), an inherent viscosity of 1.5, a tenacity of 2.4 g.p.d., an elongation of 71%, a modulus of 20 g.p.d., and a work recovery of 80%.
- the fiber cut length is 1.5 inch (3.81 cm.).
- the cotton fibers employed in this run are combed El Paso cotton (middling grade). It is observed that 50% of the cotton fibers are 1%; inches (2.
- a picker blend totalling five pounds (2.27 kg.) is made, employing as starting materials the weights of the various fibers required to give the weight percentages indicated in the table.
- the picker lap is carded into sliver, drawn, and converted into roving.
- the roving is spun into a 40s cotton count yarn.
- the yarn is woven into a plain weave fabric having a loom construction of 96 sley x 56 picks per inch (38 X 22 per c1n.).
- the fabrics are finished by scouring, vacuuming to remove water, drying at 250 F. (121 C.), heat setting the dried fabric for 3 minutes at an oven temperature of 375 F.
- the fabrics containing cotton have a finished Weight of 3.05:0.25 0z./yd. (104:9 g./m. in each instance while the fabrics containing rayon have a finished weight of 35:04 oz./yd. (119:14 g./m.
- the fabrics are evaluated for wash-wear performance by washing them in a home model washing machine using water at 35-38" C. with a commercially available detergent for home laundry use, rinsing the fabric in water at 35-38 C., spin drying, and then hanging in a still atmosphere until fully dry (216 hours).
- the fabrics are then evaluated by a group of persons on an arbitrary subjective scale using the following ratings:
- the polyethylene terephthalate fibers employed in making the 65% polyethylene terephthalate/35% rayon blend are standard, 1.5 denier, semidull, normal tenacity polyethylene terephthalate staple having a cut length of 1.5 inches (3.81 cm.) (standard polyethylene terephthalate staple produced by E. I. du P-ont de Nemours & Company, Inc. as Type 54).
- the polyethylene terephthalate fibers employed in making the 65 polyethylene terephthalate/ 35% cotton blend are standard 1.5 denier, semidull, pill resistant polyethylene terephthalate staple designed for blends with cotton and having a cut length of 1.5 inches (3.81 cm.) (polyethylene terephthalate staple for blends with cotton produced by E. I. du Pont de Nemours & Company, Inc. as type 35).
- the wash-wear rating for the fabrics of the cotton-containing blend was 1.5 while that of the rayon staple-containing blend was 1.7.
- Cotton Rayon umoumoawo The 100% citton fabric in the above series has a bulk of 2.7 cc./g., and it is observed that the fabrics of all of the cotton/polypivalolactone staple fiber blends exhibit comparable or superior bulk, ranging from 2.6 to 2.9 cc./g. This is in contrast to the fabric of cotton/polyethylene terephthalate staple fiber blend, which exhibits a relatively poorer bulk of only 2.3 cc./g. although the fabric weight is identical. Similarly, the 100% rayon fabric has a bulk of 2.3 cc./ g.
- rayon/polypivalolactone staple fiber blends exhibit comparable bulk, ranging from 2.3 to 2.5 cc./g., while the fabric of rayon/ polyethylene terephthalate staple fiber blend exhibits a relatively poorer bulk of only 2.1 cc./ g.
- a three-component blend is prepared, employing 30% of the polypivalolactone fibers, 60% combed Peeler cotton fibers, and 10% standard, 2.3 denier, polyhexamethylene adipamide staple fibers having a cut length of 1 /2 inches (3.81 cm.) (standard polyhexamethylene adipamide staple produced by E. I. du Pont de Nemours & Company, Inc. as Type 420).
- Fabric produced as described above from this blend has a Wash-wear rating of 2.1.
- the weight of the fabric is 3.26 oz./yd. (111 g./m. and its bulk is 3.1 cc./ g.
- a similar three-component blend prepared from polypivalolactone fibers, 70% combed Peeler cotton fibers, and 10% polyhexamethylene adipamide fibers is worked up into a fabric exhibiting a wash-wear rating of 1.6. Its weight is 3.50 oz./yd. (119 g./1n. and its bulk is 2.36 cc./g.
- the wash-wear performance of a fabric depends upon three important factors: the nature of the constituent fibers, the construction of the fabric, and the laundering conditions.
- the evaluation of the various fibers and blends thereof in a plain weave fabric is shown since the plain weave construction is one of the most difficult in which to attain adequate wash-wear performance and represents a severe test of the fibers.
- a change of the fabric construction to any of the various twills results in correspondingly higher wash-wear ratings for each of the fibers and blends thereof.
- the laundering conditions employed in the example represent a severe test, corresponding to laundering in a home with no automatic dryer available and the clothes hung indoors.
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- Mechanical Engineering (AREA)
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- Artificial Filaments (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US447081A US3379001A (en) | 1965-04-09 | 1965-04-09 | Blends of cellulosic and polypivalolactone staple fibers |
| NL666605564A NL147797B (nl) | 1965-04-09 | 1966-04-26 | Vezelmengsel uit cellulosehoudende vezels, bijvoorbeeld katoen en synthetische vezels. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US447081A US3379001A (en) | 1965-04-09 | 1965-04-09 | Blends of cellulosic and polypivalolactone staple fibers |
| NL666605564A NL147797B (nl) | 1965-04-09 | 1966-04-26 | Vezelmengsel uit cellulosehoudende vezels, bijvoorbeeld katoen en synthetische vezels. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3379001A true US3379001A (en) | 1968-04-23 |
Family
ID=26644028
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US447081A Expired - Lifetime US3379001A (en) | 1965-04-09 | 1965-04-09 | Blends of cellulosic and polypivalolactone staple fibers |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US3379001A (enrdf_load_stackoverflow) |
| NL (1) | NL147797B (enrdf_load_stackoverflow) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3547891A (en) * | 1969-04-02 | 1970-12-15 | Eastman Kodak Co | Heat formable polyester film |
| US3546756A (en) * | 1967-08-17 | 1970-12-15 | Kanebo Ltd | Method for manufacturing textile products having improved crease resistance |
| US3604470A (en) * | 1969-03-07 | 1971-09-14 | Burlington Industries Inc | Durable-press stretch fabric and method of obtaining same |
| US3686850A (en) * | 1969-12-19 | 1972-08-29 | Ici Ltd | Staple fibers for blends |
| US3751767A (en) * | 1971-01-28 | 1973-08-14 | Kendall & Co | Process for the formation of fibrous webs of staple fiber from continuous textile filaments |
| US3775960A (en) * | 1969-10-08 | 1973-12-04 | Kanegafuchi Spinning Co Ltd | Sewing thread and a method of preparing same |
| US4481256A (en) * | 1980-09-18 | 1984-11-06 | Kanebo, Ltd. | Wadding materials |
Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2658055A (en) * | 1951-08-24 | 1953-11-03 | Du Pont | Orientable condensation polymers of hydroxypivalic acid and process for preparing them |
| US2701406A (en) * | 1952-07-09 | 1955-02-08 | Bloch Godfrey | Fabric and method of making same |
| US2745240A (en) * | 1950-05-18 | 1956-05-15 | Bates Mfg Co | Composite filament and staple yarn |
| GB766347A (en) * | 1953-12-16 | 1957-01-23 | Ici Ltd | Synthetic polyester fibres |
| US2887468A (en) * | 1954-03-11 | 1959-05-19 | Eastman Kodak Co | Copolyesters of a glycol, a dicarboxylic acid and a hydroxy carboxylic acid |
| US2897042A (en) * | 1955-06-30 | 1959-07-28 | Du Pont | Method for increasing pill resistance and density of blended staple polyethylene terephthalate and cellulosic fabrics by applying specific chemical shrinking agents for the polyethylene terephthalate |
| US2985940A (en) * | 1955-11-30 | 1961-05-30 | Du Pont | Production of high bulk fabrics from staple fiber mixtures |
| US3016683A (en) * | 1958-10-01 | 1962-01-16 | Columbian Rope Co | Blended fiber rope |
| US3044250A (en) * | 1957-06-28 | 1962-07-17 | Du Pont | Textile product |
| US3299171A (en) * | 1964-04-20 | 1967-01-17 | Du Pont | Fibers of modified polypivalolactone |
-
1965
- 1965-04-09 US US447081A patent/US3379001A/en not_active Expired - Lifetime
-
1966
- 1966-04-26 NL NL666605564A patent/NL147797B/xx unknown
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2745240A (en) * | 1950-05-18 | 1956-05-15 | Bates Mfg Co | Composite filament and staple yarn |
| US2658055A (en) * | 1951-08-24 | 1953-11-03 | Du Pont | Orientable condensation polymers of hydroxypivalic acid and process for preparing them |
| US2701406A (en) * | 1952-07-09 | 1955-02-08 | Bloch Godfrey | Fabric and method of making same |
| GB766347A (en) * | 1953-12-16 | 1957-01-23 | Ici Ltd | Synthetic polyester fibres |
| US2887468A (en) * | 1954-03-11 | 1959-05-19 | Eastman Kodak Co | Copolyesters of a glycol, a dicarboxylic acid and a hydroxy carboxylic acid |
| US2897042A (en) * | 1955-06-30 | 1959-07-28 | Du Pont | Method for increasing pill resistance and density of blended staple polyethylene terephthalate and cellulosic fabrics by applying specific chemical shrinking agents for the polyethylene terephthalate |
| US2985940A (en) * | 1955-11-30 | 1961-05-30 | Du Pont | Production of high bulk fabrics from staple fiber mixtures |
| US3044250A (en) * | 1957-06-28 | 1962-07-17 | Du Pont | Textile product |
| US3016683A (en) * | 1958-10-01 | 1962-01-16 | Columbian Rope Co | Blended fiber rope |
| US3299171A (en) * | 1964-04-20 | 1967-01-17 | Du Pont | Fibers of modified polypivalolactone |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3546756A (en) * | 1967-08-17 | 1970-12-15 | Kanebo Ltd | Method for manufacturing textile products having improved crease resistance |
| US3604470A (en) * | 1969-03-07 | 1971-09-14 | Burlington Industries Inc | Durable-press stretch fabric and method of obtaining same |
| US3547891A (en) * | 1969-04-02 | 1970-12-15 | Eastman Kodak Co | Heat formable polyester film |
| US3775960A (en) * | 1969-10-08 | 1973-12-04 | Kanegafuchi Spinning Co Ltd | Sewing thread and a method of preparing same |
| US3686850A (en) * | 1969-12-19 | 1972-08-29 | Ici Ltd | Staple fibers for blends |
| US3751767A (en) * | 1971-01-28 | 1973-08-14 | Kendall & Co | Process for the formation of fibrous webs of staple fiber from continuous textile filaments |
| US4481256A (en) * | 1980-09-18 | 1984-11-06 | Kanebo, Ltd. | Wadding materials |
Also Published As
| Publication number | Publication date |
|---|---|
| NL6605564A (enrdf_load_stackoverflow) | 1967-10-27 |
| NL147797B (nl) | 1975-11-17 |
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