US3434874A - Acrylic fibers - Google Patents

Acrylic fibers Download PDF

Info

Publication number
US3434874A
US3434874A US491046A US3434874DA US3434874A US 3434874 A US3434874 A US 3434874A US 491046 A US491046 A US 491046A US 3434874D A US3434874D A US 3434874DA US 3434874 A US3434874 A US 3434874A
Authority
US
United States
Prior art keywords
yarn
finish
knitting
yarns
fibers
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
Application number
US491046A
Other languages
English (en)
Inventor
Thomas Jefferson Proffitt Jr
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Application granted granted Critical
Publication of US3434874A publication Critical patent/US3434874A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/244Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
    • D06M13/282Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
    • D06M13/292Mono-, di- or triesters of phosphoric or phosphorous acids; Salts thereof
    • D06M13/295Mono-, di- or triesters of phosphoric or phosphorous acids; Salts thereof containing polyglycol moieties; containing neopentyl moieties
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M7/00Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/40Reduced friction resistance, lubricant properties; Sizing compositions
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • Y10T428/2929Bicomponent, conjugate, composite or collateral fibers or filaments [i.e., coextruded sheath-core or side-by-side type]
    • Y10T428/2931Fibers or filaments nonconcentric [e.g., side-by-side or eccentric, etc.]
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • Y10T428/2933Coated or with bond, impregnation or core
    • Y10T428/2964Artificial fiber or filament
    • Y10T428/2967Synthetic resin or polymer
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • Y10T428/2933Coated or with bond, impregnation or core
    • Y10T428/2964Artificial fiber or filament
    • Y10T428/2967Synthetic resin or polymer
    • Y10T428/2969Polyamide, polyimide or polyester

Definitions

  • This invention relates to a finishing of synthetic fibers, and in particular concerns finishing compositions which will result in spun yarns having good knittability. It is also concerned with finishes which will prevent the accumulation of static charges on the finished fibers.
  • Knitting yarns spun from staple fibers have low twist in order to obtain high bulk, and, as a result of the low twist the yarns have low strength, usually expressed as Lea Product. Knitting imposes a stress on the yarn and some yarns require special finishes to make them strong enough to knit and to reduce stress in knitting. Such yarns can be treated with a wax at the knitting machine but this is inconvenient, can result in accidental choice of an improper wax and it is ditficult to apply finish uniformly at this state. Such finishes often cause difficulties in dyeing because of non-uniformity.
  • the present invention provides a fiber treated with a wax-containing finish, which fiber will process satisfactorily through carding and spinning or through cutting on the Pacific Converter to give yarns which will knit satisfactorily without application of wax by the knitter. It also provides a fiber which will not accumulate a static charge during processing.
  • finish composition consisting essentially of paraffin wax and certain monoand diesters of phosphoric acid. Finish of this composition is applied by the filament manufacturer and results in a finish-containing filament that can be processed without difficulty in the usual manner, for example cut to staple and then spun to yarn, and after such processing can be used by knitting manufacturers without the need to apply at the knitting machines the special waxes heretofore necessary.
  • the phosphate esters in compositions according to the present invention are known and available commercially. These esters are made from fatty alcohols or alkyl phenols which have been condensed with an alkylene oxide, preferably ethylene oxide or propylene oxide.
  • the phosphoric esters are used in the form of their alkali, alkaline earth, ammonium, amine or quaternary ammonium salts.
  • alcohols and alkyl phenols most suitable for making phosphoric acid esters for use in the present invention are the following: Lauryl or decyl alcohol condensed with 2 to 0 mols alkylene oxide; tetradecyl alcohol, hexadecyl alcohol or hexadecenyl alcohol condensed with 4 to 16 mols alkylene oxide; nonyl or decyl phenol condensed with 4 to 16 mols alkylene oxide; and octyl phenol condensed with 3 to 14 mols alkylene oxide.
  • the phosphoric esters can be either monoor diesters or, more conveniently, a mixture of the monoand diesters.
  • the alcohols can likewise consist of mixtures and need not be a single specie.
  • a preferred composition is prepared by heating together a paratfin wax melting at 50 to 55 C. with a mixture of the monoand diesters of phosphoric acid made by reacting phosphoric acid with a product made by condensing lauryl alcohol with 4 mols ethylene oxide.
  • the phosphoric acid ester is preferably used in the form of its sodium salt.
  • the finish composition of this invention is particularly suited to low strength yarns, that is, yarns of low Lea Product.
  • the finish lubricates yarn to which it is applied and increases the strength, but more importantly it lowers the yarn-to-metal friction which decreases the running tension when the yarn is knit resulting in better knitting qualities.
  • the yarn-to-yarn boundary friction is slightly decreased with a typical value of 0.21 where a control yarn having a conventional finish has a coefficient of 0.23.
  • the hydrodynamic yarn-to-metal friction for a typical yarn is 0.26 versus 0.32 for a control yarn.
  • the lower stress in the yarn during knitting, which results from the finish on the fiber means fewer breaks and less defects in the knit fabric.
  • Another property of finishes of this invention is a high degree of thixotrophy as shown by a high viscosity at low shear and low viscosity at high shear.
  • the finishes of this invention are especially useful for acrylic fibers of any of the usual deniers for textile applications but can also be used on other synthetic fibers, not only to improve knitting, but to lower static.
  • a concentration of 0.1 to 0.8% finish, and preferably 0.1 to 0.5%, based on fiber weight, is satisfactory. Higher concentrations within this range will reduce static to satisfactory levels at relative humidities as low as 20%. At higher relative humidities, lower concentrations of finish can be used.
  • the finish can be applied by spraying, roller coating or any other known method as suits the convenience of the operator.
  • Fibers finished according to this invention can be converted to yarns by the staple route or by treating tow on the Pacific Converter in which the tow is cut in a diagonal manner and converted to sliver.
  • the knittability of yarns is determined as follows: Two yarns are used as standards, one of which is known to knit satisfactorily commercially (No. 1) and one which knits with ditficulty (No. 2) because of breaks which result in holes in the knitted fabric. Knitting is done on a. 2l-gauge full-fashioned machine. The number of courses per inch on the machine is adjusted until breaks and holes occur with both yarns. Under these conditions, the satisfactory yarn (No. l) develops 2 to 10 holes in 15 minutes of knitting whereas the poor yarns (No. 2) develops 40 to holes in 15 minutes. vAny other yarn developing no more than 10 holes in 15 minutes of knitting is considered satisfactory.
  • a bicomponent fiber is spun from two polymer compositions as follows:
  • Parts Composition I Polyacrylonitrile 100 3
  • Composition H Parts Terpolymer of:
  • This finish dispersion is applied to the tow by spraying so as to leave 0.3% of finish on the fiber after drying.
  • the tow is then converted to sliver on a Pacific Converter (described in U.S. Patent 2,438,469 to Wilkie).
  • the sliver is pin drafted and spun into 2/30 Worsted count (530 denier) yarn with 11 Z turns per inch (4.3 per cm.) in the singles and 5.7 S turns per inch (2.2 per cm.) in the ply.
  • This yarn is found to have a Lea Product of 1273.
  • Sweaters knit from this yarn are found to be free from pills after 100 hours of wear. This shows that the yarn is made of Weak fibers which ordinarily will not knit, but as a result of the finish the yarn knits satisfactorily. No static is developed during the processing of these fibers or the knitting of these yarns.
  • EXAMPLE II This example is to show that staple fiber finished in accordance with this invention can be carded, drafted, and spun satisfactorily.
  • a tow of 470,000 denier is prepared and finished as in Example I. It is next passed through a stuffer-box crimper to impart 10 to 15 crimps per inch (3.9 to 5.9 crimps per cm.). It is then cut into staple in lengths from 2.5 inches to 5.5 inches (6.3 to 14 cm.). This staple is carded on the Worsted system and spun into 30 Worsted count (266 denier) singles yarn with 11 Z turns per inch (4.3 per cm.) and two-piled with 6 S turns per inch (2.4 per cm.) in the ply.
  • EXAMPLE III Dispersions are made of the finish of Example I at solids concentrations of and The 25% dispersion has a viscosity of 209 centistokes and is capable of being applied to tow by conventional methods but the 30% dispersion is much too viscous for satisfactory application. Both of these dispersions are highly thixotrophic.
  • Bicomponent textile fibers of synthetic acrylic polymer having on the surfaces thereof a finish composition consisting essentially, by weight, of 1.25 to 1.75 parts of a salt of a partial ester of phosphoric acid per part of a paraffin wax, said salt being an alkali metal salt of a monoor diester of phosphoric acid and at least one member of the group consisting of the condensation product of lauryl alcohol with 2 to 10 mols of alkylene oxide, the condensation product of decyl alcohol with 2 to 10 mols of alkylene oxide, the condensation product of tetradecyl alcohol with 4 to 16 mols of alkylene oxide, the condensation product of hexadecyl alcohol with 4 to 16 mols of alkylene oxide, the condensation product of hexadecenyl alcohol with 4 to 16 mols of alkylene oxide, the condensation product of nonyl phenol with 4 to 16 mols of alkylene oxide, the condensation product of decyl phenol with 4 to 16 mols of alky
  • Textile fibers comprising bicomponent acrylic fibers in which the components are in side-by side relation along their length, one of the components being a polyacrylonitrile polymer and the other being a mixture of terpolyrner of acrylonitrile, methyl acrylate and sodium styrenesulfonate and copolymer of acrylonitrile and sodium styrenesulfonate, the fibers having on their surfaces about 0.1 to 0.8 percent, based on the fiber weight, of a finish composition consisting essentially of parts by weight of refined paraffin wax and parts by weight of the sodium salt of a mixture of monoand diesters of phosphoric acid and the condensate of lauryl alcohol with 4 mols of ethylene oxide.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
US491046A 1965-09-28 1965-09-28 Acrylic fibers Expired - Lifetime US3434874A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US49104665A 1965-09-28 1965-09-28

Publications (1)

Publication Number Publication Date
US3434874A true US3434874A (en) 1969-03-25

Family

ID=23950571

Family Applications (1)

Application Number Title Priority Date Filing Date
US491046A Expired - Lifetime US3434874A (en) 1965-09-28 1965-09-28 Acrylic fibers

Country Status (3)

Country Link
US (1) US3434874A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
GB (1) GB1102318A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
NL (1) NL6613540A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3658573A (en) * 1969-04-08 1972-04-25 Eastman Kodak Co Support provided with antistatic layer
US3907689A (en) * 1973-08-29 1975-09-23 Eastman Kodak Co Textile treating composition and textile yarn treated therewith
US3953651A (en) * 1972-11-14 1976-04-27 Japan Exlan Company Limited Acrylic synthetic fiber having animal hair-like hand
US4115351A (en) * 1973-11-12 1978-09-19 Yasushi Joh Flame retardant composition
US4210700A (en) * 1978-09-15 1980-07-01 Allied Chemical Corporation Production of polyester yarn
EP0416917A3 (en) * 1989-09-07 1991-08-28 Kao Corporation Spinning lubricant composition for acrylic fibre
WO2004069980A1 (de) * 2003-02-10 2004-08-19 Cognis Ip Management Gmbh Textilausrüstungsmittel

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB835797A (en) * 1956-05-14 1960-05-25 Boehme Fettchemie Gmbh Process for waterproofing
US3038236A (en) * 1954-02-26 1962-06-12 Du Pont Crimped textile products
US3056744A (en) * 1957-09-18 1962-10-02 Gen Aniline & Film Corp Textile assistant
US3113369A (en) * 1960-05-02 1963-12-10 Monsanto Chemicals Yarn manufacture and products obtained thereby

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3038236A (en) * 1954-02-26 1962-06-12 Du Pont Crimped textile products
GB835797A (en) * 1956-05-14 1960-05-25 Boehme Fettchemie Gmbh Process for waterproofing
US3056744A (en) * 1957-09-18 1962-10-02 Gen Aniline & Film Corp Textile assistant
US3113369A (en) * 1960-05-02 1963-12-10 Monsanto Chemicals Yarn manufacture and products obtained thereby

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3658573A (en) * 1969-04-08 1972-04-25 Eastman Kodak Co Support provided with antistatic layer
US3953651A (en) * 1972-11-14 1976-04-27 Japan Exlan Company Limited Acrylic synthetic fiber having animal hair-like hand
US3907689A (en) * 1973-08-29 1975-09-23 Eastman Kodak Co Textile treating composition and textile yarn treated therewith
US3951825A (en) * 1973-08-29 1976-04-20 Eastman Kodak Company Textile treating composition and textile yarn treated therewith
US4115351A (en) * 1973-11-12 1978-09-19 Yasushi Joh Flame retardant composition
US4210700A (en) * 1978-09-15 1980-07-01 Allied Chemical Corporation Production of polyester yarn
EP0416917A3 (en) * 1989-09-07 1991-08-28 Kao Corporation Spinning lubricant composition for acrylic fibre
US5282871A (en) * 1989-09-07 1994-02-01 Kao Corporation Spinning lubricant composition for acrylic fiber
WO2004069980A1 (de) * 2003-02-10 2004-08-19 Cognis Ip Management Gmbh Textilausrüstungsmittel
US20060258558A1 (en) * 2003-02-10 2006-11-16 Rolf Wachter Textile finishing agents
US7309685B2 (en) 2003-02-10 2007-12-18 Cognis Ip Management Gmbh Textile finishing agents for imparting a sensory effect during use

Also Published As

Publication number Publication date
NL6613540A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) 1967-03-29
GB1102318A (en) 1968-02-07

Similar Documents

Publication Publication Date Title
CA2054277C (en) Cardable hydrophobic polyolefin fiber, material and method for preparation thereof
US2842462A (en) Antistatic synthetic textile material
US2461043A (en) Process of conditioning cellulose ester filaments
EP0312677B1 (de) Mittel zum Glätten von Textilfasermaterialien
US3434874A (en) Acrylic fibers
US3518184A (en) Textile fiber finish composition
US2717842A (en) Antistatic treatment and treated products
US2976186A (en) Treated textile fiber
JP2669559B2 (ja) アクリル繊維用紡績油剤
US2735790A (en) Ttnitehi
US4297407A (en) Finish composition for the spinning of highly crimped cellulose fibers using a composition cont. fatty acid ester, organic phosphoric acid ester, fatty acid ethylene oxide cond. prod. and fatty acid salt
EP0010764B1 (en) Polypropylene yarn product of improved stability and method for preparing a textile material
EP0309253A2 (en) Dyeable polypropylene fibres for clothes
US3888775A (en) Oil composition for synthetic staple fibers
US2436219A (en) Textile product and process
CA2027661A1 (en) Aramid fibers with deposit-free finish
JPS63112769A (ja) ポリエステル短繊維
DE3324662A1 (de) Hydrophile polyester-stapelfaser, verfahren zu ihrer herstellung und daraus hergestelltes textilmaterial
US2717877A (en) Antistatic compositions
US3297570A (en) Yarn treating compositions
US2292211A (en) Yarn conditioning process
US2286793A (en) Yarn conditioning process and composition therefor
US2828229A (en) Cellulose fibres coated with cotton wax
Gupta et al. Chemically texturizing jute and jute-polypropylene blended yarns
Simpson et al. An analysis of carding efficiency and processing performance of cotton/polyester blends