US2875019A - Method for producing crimped filaments - Google Patents
Method for producing crimped filaments Download PDFInfo
- Publication number
- US2875019A US2875019A US559709A US55970956A US2875019A US 2875019 A US2875019 A US 2875019A US 559709 A US559709 A US 559709A US 55970956 A US55970956 A US 55970956A US 2875019 A US2875019 A US 2875019A
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- US
- United States
- Prior art keywords
- filaments
- groups
- active agent
- amine groups
- drum
- 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
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- 238000004519 manufacturing process Methods 0.000 title description 7
- 239000004094 surface-active agent Substances 0.000 claims description 28
- 229920005989 resin Polymers 0.000 claims description 23
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- 238000000034 method Methods 0.000 claims description 18
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- 150000001875 compounds Chemical class 0.000 claims description 8
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- 229910052783 alkali metal Inorganic materials 0.000 claims description 7
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims description 5
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 4
- 239000010452 phosphate Substances 0.000 claims description 4
- 150000003141 primary amines Chemical group 0.000 claims description 3
- 150000003335 secondary amines Chemical group 0.000 claims description 3
- 150000003512 tertiary amines Chemical group 0.000 claims description 3
- 150000001412 amines Chemical group 0.000 claims description 2
- 150000002148 esters Chemical group 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- -1 polyethylene Polymers 0.000 description 11
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 229920006038 crystalline resin Polymers 0.000 description 7
- 239000000243 solution Substances 0.000 description 6
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- 150000001340 alkali metals Chemical class 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
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- 125000003277 amino group Chemical group 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 125000004185 ester group Chemical group 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 230000003381 solubilizing effect Effects 0.000 description 3
- 229920005992 thermoplastic resin Polymers 0.000 description 3
- ZGHFDIIVVIFNPS-UHFFFAOYSA-N 3-Methyl-3-buten-2-one Chemical compound CC(=C)C(C)=O ZGHFDIIVVIFNPS-UHFFFAOYSA-N 0.000 description 2
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- 239000004677 Nylon Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000011149 active material Substances 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- FXDDASGKIJJAQS-UHFFFAOYSA-N (octadecylamino)methanol Chemical compound CCCCCCCCCCCCCCCCCCNCO FXDDASGKIJJAQS-UHFFFAOYSA-N 0.000 description 1
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 1
- LIFLRQVHKGGNSG-UHFFFAOYSA-N 2,3-dichlorobuta-1,3-diene Chemical compound ClC(=C)C(Cl)=C LIFLRQVHKGGNSG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ZJZJKRFYHSRMNR-UHFFFAOYSA-N Cl[C]=C Chemical compound Cl[C]=C ZJZJKRFYHSRMNR-UHFFFAOYSA-N 0.000 description 1
- 229920004934 Dacron® Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical compound ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 229920004933 Terylene® Polymers 0.000 description 1
- 241001416177 Vicugna pacos Species 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- QGVQVNIIRBPOAM-UHFFFAOYSA-N dodecyl naphthalene-1-sulfonate;sodium Chemical class [Na].C1=CC=C2C(S(=O)(=O)OCCCCCCCCCCCC)=CC=CC2=C1 QGVQVNIIRBPOAM-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 229960004756 ethanol Drugs 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical class 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- ZHALDANPYXAMJF-UHFFFAOYSA-N octadecanoate;tris(2-hydroxyethyl)azanium Chemical compound OCC[NH+](CCO)CCO.CCCCCCCCCCCCCCCCCC([O-])=O ZHALDANPYXAMJF-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229940068918 polyethylene glycol 400 Drugs 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229940096992 potassium oleate Drugs 0.000 description 1
- 229940114930 potassium stearate Drugs 0.000 description 1
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 239000012260 resinous material Substances 0.000 description 1
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N salicylic acid phenyl ester Natural products OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- 229940082004 sodium laurate Drugs 0.000 description 1
- 229940045870 sodium palmitate Drugs 0.000 description 1
- GGXKEBACDBNFAF-UHFFFAOYSA-M sodium;hexadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCC([O-])=O GGXKEBACDBNFAF-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229940037312 stearamide Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229940029614 triethanolamine stearate Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/22—Formation of filaments, threads, or the like with a crimped or curled structure; with a special structure to simulate wool
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/04—Polyester fibers
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/10—Polyvinyl halide esters or alcohol fiber modification
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/21—Nylon
Definitions
- This invention relates to the production of fine crimped fusible to form very fluid melts.
- crystalline resins such as the vinylidene chloride, nylon, polyethylene, polydichlorobutadiene and other crystalline high polymeric resinous materials.
- crimped, wool-likefilaments may be manufactured from the crystalline resins by melt-extruding an array of filaments versely of the filaments after they emerge from the die, quenching the filaments in a coolant, and cold-stretching the filaments to convert them to the oriented-crystalline state. After the cold-stretching, the tension is released from the filaments and the uneven strains therein cause the filaments to retract slightly and become crimped and curly. This relaxation is not as rapid as might be desired, apparently (in the light of the present invention) due to the clinging together of the filaments while still blowing cold air transt wet from the quenching bath; usually the retraction is not complete until the filaments have completely dried. This is both timeconsuming and also results in a less complete retraction and crimping of the filaments. Accordingly, it is an object of this invention. to provide a novel and improved method for the of crimped filaments from crystalline'resins.
- Another object is to provide a process of the type abovedescribed in which the filaments are 'exposedto a cold air blast, quenched, oriented, and. relaxed, in'which the relaxation of the filaments takes place substantially immediately upon removal of tension therefrom.
- a further object is to provide such a process which will result in filaments having improved. and more pronounced crimp.
- Fig. 1 is a general diagrammatic view of the employed in this invention
- Fig. 2 is a detailed side view of the extruding die and employed in this invention; and Fig. 3 is a sectional view along line 33 of Fig. 2.
- the more rapid relaxation and kinking obtained in accordance with this invention avoids the necessity for and space for the filaments while they are relaxing. Also the more rapid relaxation accordance with thisinvention results in a more pronounced and resilient kinking of the filaments;the delay in-relaxationincurred with solution of asurface-active agent is distributed upon the filaments at a point subsequent to the orientation of the filaments, and in which the manufacture e as Terylene or 2,875,019 iatented eb. 24, 19559 THE CRYSTALLINE RESINS
- the resins employed in the manufacture of kinked filamerits in accordance with this invention are of the special class known as crystalline resins.
- These resins are solid state, the long molecular chains of these resins tend to associate together locally to produce crystalline regions. If these resins are formed into filaments, as for instance by extrusion in the heat-softened state, and the filaments are thereafter subjected to stretching, these crystalline .aggregates become aligned lengthwise in the direction of stretching and impart a high degree of strength and flexibility to the resultant filaments.
- Resins of this type are well known, and include for'instance the vinylidene chloride resins, which are polymers of vinylidene chloride and copolymers thereof with up to 20% of other unsaturated compounds copolymerizable therewith, such for example, as vinyl chloride, vinyl fluoride, vinyl acetate, styrene, esters of acrylic and methacrylic acids such as methyl methacrylate, and ethyl methacrylate, acrylonitrile, vinyl typeethers and ketones such as methyl vinyl ether, methyl vinyl ketone and related compounds such as methyl isopropenyl ketone and the like.
- vinylidene chloride resins which are polymers of vinylidene chloride and copolymers thereof with up to 20% of other unsaturated compounds copolymerizable therewith, such for example, as vinyl chloride, vinyl fluoride, vinyl acetate, styrene, esters of acrylic and methacrylic acids such as methyl methacryl
- the invention is also applicable to the processing into curly crimped filaments of othercrystalline resins, such for instance as the nylon resins, which are high molecular weight condensation products of dicarboxylic acidswith diamines or of amino acids alone or of mixtures of amino acids with dicarboxylic acids and diarnines;
- Dacron which are condensation prodnets of terephthalic acid and ethylene glycol; polyethylene; and polymers of 2,3-dichlorobutadiene-1,3 such as described in the patent to Kuhn 2,451,195. All of these resins maybe processed in accordance with this inventio-ninto crimped fibers having excellent curliness, loft andfeelz' i
- kinked filaments of crystalline resins may be produced by melt-extruding extruded filaments, and quenching, orienting andrelaxingthe filaments. The process may take various forms; for instance, air maybe blown upon thefilaments from all sides as they emerge from the extrusion die.
- An advantageous means for achieving thispurpo'se consists in 'an arrangement in which theextruding dies have the orifices thereof arranged in a circle in a horizontal plane with the orifices opening downwardly, normal to the plane of said circle;
- Theemerging filaments are conducted vertically downwardly from said orifices, so that they form a substantially cylindrical array-i. e., at the orifice the filaments are all substantially parallel to.each other and equidistant from and substantially parallel to an axis drawn perpendicular with the center of the circle upon which the orifices of the die are disposed.
- this extruding head comprises a conical distributing passage 14 into which the molten resin is forced by the extruding machine 10, which receiving passage leads downward to the periphery of a die 16.
- the face of this die 16 is disposed in a horizontal plane and is provided with a large number of die orifices 18 communicating with the conical passage 14 from which they receive the molten resin under pressure and extrude it as filaments 20.
- These orifices are arranged in a circle having its center at the center 22 of the die 16, and it will be seen that the filaments 20 are extruded downwardly in a substantially vertical direction equidistant from an axis 24 drawn through the center 22 and perpendicular to the face of the die 16.
- the description of the filaments 20 as being in a cylindrical array is approximate only: they will be deflected outwardly by cooling air as described below. 'Countervailing this, the filaments will usually also be drawn inwardly into a frusto-conical array, since they aregathered together in passing over the guides 26 in the quenching bath 28.
- the array of filaments may be designated cylindrical.
- Means are provided for directing a flow of cooling air or other gas radially in all directions away from the axis of the cylindrical array of extruded filaments and outwardly past the extruded filaments.
- This flow of coolling air is indicated by the arrows 30.
- this means comprises an air jet 32 mounted upon a bracket arm 33 attached to the wall of a quenching tank into which the filaments ultimately fall.
- This air jet is directed upwardly and concentrically of the cylindrical array of filaments so as to project a stream ofair (indicated by the arrows 34) against a discoidal deflector plate 36 which is suspended from the extrusion die 16 in a position immediately below the die and coaxial of the cylindrical array of filaments.
- the air from the jet impinging upon this deflector plate is deflected radially outwardly and away from the axis24 of the cylindrical array of filaments in all directions past the freshly extruded filaments 20.
- This air flow effects two purposes; first it rapidly chills the skin surface of the filaments and does do in a non-uniform manner, the greatest cooling effect being on that side of any given filament facing the axis of the cylindrical array of filaments thereby setting up uneven strains in the filaments; likewise, the flow of air appears to induce vibrations in the freshly extruded filaments, setting up varying strains in the filaments distributed periodically lengthwise of the filaments.
- the filaments after passing the outwardly-directed flow 30 of cooling air, drop into a tank 28 of cooling water 40.
- the filaments thereby become chilled and completely solidified, whereby the strains induced as above discussed become preserved therein.
- the filaments then pass down through the bath under a set of guide, pins 26 and thence upward through and out of the bath to and over a guide roll 41 to a pair of drawing rolls 42,.
- the drawing rolls are driven at a peripheral speed in l excess of the linear velocity at which the filaments are extruded; due to the'resistance of the water 40 andto some extent the friction of the pins 26, a considerable tension is induced in the filaments and they are stretched to several times their extruded length during their passage through the bath and to the drawing rolls, whereby the filaments are drawn into an oriented crystalline form.
- the filaments pass from the drawing rolls 42 to a windup drum 44 upon which the filaments are accumulated as a skeina
- a revolving roll 43 dipping into a trough 45 containing asolution or emulsion 47 of a surface-active agent bears against the windup drum so as to apply a regulated amount of the surface-active agent to the filaments as they accumulate upon the drum.
- the surface-activeagent solution may also be applied in a number of other ways. For example, a constant regulated stream may be applied from an overhead reservoir directly onto the filament as it is wound upon drum 44. Alternatively the solution rfiay be pumped from a reservoir and applied directly.
- the filament may pass over an applicator arrangement similar to the assembly 43, 45 prior to reaching drum 44.
- the filament is cut and transferred to a second windup roll 46 so as to be wound and accumulated upon the second windup roll.
- the accumulated fila ment is then stripped from the first winduproll.
- the stripped filaments contract and, due to the uneven strains set up by the action of the air flow to which they were subjected between the extruder and the quenching bath, this contraction takes place with the formation of kinks and curls which are quite sharp and close. contrast to theresults obtained when the identical process is carried out without the application of the surface-active agentsolution 47;in such case the filaments must be hung up' in a relaxed condition for several hours in order to develop the kinks.
- an applicator roll 49 similar to the applicator roll 43 bears against the windup drum and is arranged to apply the solution 47 of the wetting agent to the filaments as they accumulate on the drum.
- the filament is again cut and transferred back to the first windup drum 44, and the accumulated filament stripped from the drum 46, and so on, the filament being accumulated alternately upon the two drums 46.
- the surface-active agent applied by the rolls 43 and 49 may be any of a wide variety of such materials.
- the ordinary alkali metal and amine fatty acid soaps such as sodium laurate, sodium myristrate, sodium palmitate, potassium oleate, potassium stearate, triethanolamine stearate and the like may be employed.
- sulfateand sulfonategroup-containing surface-active agents such as the sulfonated fatty oils and fatty acids, anionic phosphated alcohols, the alkyl sulfosuccinates, the fatty alcohol sulfates.
- sulfated castor oil fatty acids sulfated coconut oil alco hol's, di-(Z-ethyl hexyl) sulfosuccinate, sodium dodecyl naphthalene sulfonates and the like.
- Other classes of surface-activeagents include the fatty amines and amides, such as dodecyl amine, hexadecyl amine, stearamide, N-stearyl methylolamide, and the like.
- surface-active agents which have the greatest antistatic action exert the most effective action in the practice of this invention, although there appears to be no apriori reason why this should be so.
- Surfaceactive agents in general may be defined as compounds containing from 8 to 22 carbon atoms coupled to highly polar solubilizing groups such as alkali metal and ammonium carboxylate groups, sulfate half-ester groups, sulfonate groups, phosphate partial ester groups, primary, secondary, tertiary and quaternary amine groups and the like.
- the surface-active agent is conveniently supplied to the applicator rolls as a 0.5 to 10% (preferably 2.0% solution in water, and a sufficient amount will .be used so that the filament takes up 0.01 to 3.0% (preferably l.()%) ofzsprface-active agent, based on the weight of the filament.
- a point which it is highly desirable to observe in the application of the surface-active agent to the filament is that it ,shall be Withhflld until after the orienting step, e. g. the cold stretching effected in advance of the drawing rolls 42. It has been found, for operational reasons, that the surface-active agents interfere with the colddrawing behavior of the filament, causing wrapping of broken filaments on rolls 42 and slippage of the main filament band resulting in uneven orienting stretch.
- Antistat N an anionic phosphated alcohol mixture marketed by E. I. du Pont de Nemours and Co.
- Olate flakes a relatively pure, neutral sodium oleate marketed by Armour and Co.
- Avitone A a modified anionic sodium salt of su'lfonated hydrocarbon marketed 'by E. I. du Pont de Nemours & Co.
- Zelec DP a permanent antistat having an acrylic ester resin base, marketed by E. I. du Pont de Nemours & Co. v
- G 1300 a polyoxyethylene sorbital marketed by Atlas Powder Company.
- Nacconol NR a sodium alkyl aryl sulfonate, marketed by National Aniline Division, Allied Chemical & Dye Corporation.
- Diameter of orifices 18 0.0125 inch Diameter of circle upon which the orifices are arranged: 6 inches Temperature of die 16: 170 C.
- Theoretical speed of filament extruded through orifice (assuming no contraction of diameter of filament): 132 ft. per min.
- the filaments produced as above described 'had excellent feel, handle and loft'comparable to naturally kinked fibers such as wool, alpaca and the like.
- the filaments were spun into yarn which was woven as the pile of an Axminster carpet, and in this application exhibited a'very desirable loft and showed good resistance to ordinary wear.
- the filaments were likewise found highly suitable when spun into yarns for knitting into garments, and for ordinary woven fabric.
- this invention provides a novel process and apparatus for the production of curly, kinked fine filaments of oriented crystalline resins.
- the process can be carried out With a minimum of skilled attendance and the apparatus required is both simple and inexpensive.
- the process avoids the necessity for providing a large detention space for hanging the filament to develop the curl thereof, which has heretofore been necessary in processes of the general type.
- Process which comprises melt-extruding an array of filaments of an orientable crystalline thermoplastic resin, chilling the filaments when freshly extruded by blowing air thereupon, quenching said filaments in a cooling medium, subjecting the filaments to cold drawing in the absence of a surface-active agent, applying a surface-active agent to the filaments while still under tension, and thereafter removing tension from the filaments to permit them to relax into a crimped configuration, the surface-active agent applied to the filaments being a compound containing from 8 to 22 carbon atoms coupled to a highly polar solubilizing group selected from the group consisting of alkali metal carboxylate groups, ammonium carboxylate groups, sulfate half-ester groups, sulfonate groups, phosphate partial ester groups, primary amine groups, secondary amine groups, tertiary amine groups and quaternary amine groups.
- Process which comprises melt-extruding an array of filaments of a vinylidene chloride resin, chilling the laments when freshly extruded by blowing air thereupon, quenching said filaments in a cooling medium, subjecting the filaments to cold drawing in the absence of a surface-active agent, Winding the cold-drawn filaments upon a collecting drum, applying a surface-active agent to the filaments while still under tension and wound upon said collecting drum, and stripping said filaments from said drum so as to remove tension from the filaments to permit them to relax into a crimped configuration, the surface-active agent applied to the filaments being a compound containing from 8 to 22 carbon atoms coupled to a highly polar solubilizing group selected from the group consisting of alkali metal carboxylate groups, ammonium carboxylate groups, sulfate half-ester groups, sulfonate groups, phosphate partial ester groups, primary amine groups, secondary amine groups, tertiary amine groups and quaternary amine
- Process which comprises melt-extruding an array of filaments of an orientable crystalline thermoplastic resin, chilling the filaments when freshly extruded by blowing air thereupon, quenching said filaments in a cooling medium, subjecting the filaments to cold drawing in the absence of a surface-active agent, winding the cold-drawn filaments upon a collecting drum, applying a phosphated alcohol surface-active agent containing from 8 to 22 carbon atoms to the filaments while still under tension and wound upon said collecting drum, and stripping said filaments from said drum so as to remove tension from the filaments to permit them to relax into a crimped configuration.
- Process which comprises melt-extruding an array of filaments of an orientable crystalline thermoplastic resin, chilling the filaments when freshly extruded by blowing air thereupon, quenching said filaments in a cooling medium, subjecting'the filaments to cold drawing in the absence of a surface-active agent, winding the colddrawn filaments upon a collecting drum, applying an alkali metal soap containing from 8 to 22 carbon atoms to the filaments while still under tension and wound upon said collecting drum, and stripping said filaments from said drum so as to remove tension from the filaments to permit them to relax into a crimped configuration.
- Process which comprises melt-extruding an array of filaments of a vinylidene chloride resin, chilling the filaments when freshly extruded by blowing air thereupon, quenching said filaments in a cooling medium, subjecting the filaments to cold drawing in the absence of a surface-active agent, windingthe cold-drawn filaments upon a collecting drum, applying a phosphated alcohol upon a collecting drum,
- Process which comprises melt-extruding an array of filaments of a vinylidene chloride resin, chilling the filaments when freshly extruded by blowing air thereupon, quenching said filaments in a cooling medium, subjecting the filaments to cold drawing in the absence of a surface-active agent, winding the cold-drawn filaments applying an alkali metal soap containing from 8 to 22 carbon atoms to the filaments while still under tension and wound upon said collecting drum, and stripping said filaments from said drum so as to remove tension from the filaments to permit them to relax into a crimped configuration.
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Description
Feb. 24, SPQHN EI-AL METHOD FOR PRODUCING CRIMPE'D FILAMENTS Filed Jan. 17, 1956 By MELT/37F J-sxy/m' associated equipment described in which a which no surface-active material is applied;
providing detention facilities of the filaments obtained in United States PatentO METHOD FOR PRODUCING CRIMPED FILAMENTS Application January 17, 1956, Serial N0.559,709 6 Claims. 01. lit-54) This invention relates to the production of fine crimped fusible to form very fluid melts. In the filaments of crystalline resins such as the vinylidene chloride, nylon, polyethylene, polydichlorobutadiene and other crystalline high polymeric resinous materials.
It is known that crimped, wool-likefilaments may be manufactured from the crystalline resins by melt-extruding an array of filaments versely of the filaments after they emerge from the die, quenching the filaments in a coolant, and cold-stretching the filaments to convert them to the oriented-crystalline state. After the cold-stretching, the tension is released from the filaments and the uneven strains therein cause the filaments to retract slightly and become crimped and curly. This relaxation is not as rapid as might be desired, apparently (in the light of the present invention) due to the clinging together of the filaments while still blowing cold air transt wet from the quenching bath; usually the retraction is not complete until the filaments have completely dried. This is both timeconsuming and also results in a less complete retraction and crimping of the filaments. Accordingly, it is an object of this invention. to provide a novel and improved method for the of crimped filaments from crystalline'resins.
Another object is to provide a process of the type abovedescribed in which the filaments are 'exposedto a cold air blast, quenched, oriented, and. relaxed, in'which the relaxation of the filaments takes place substantially immediately upon removal of tension therefrom. A further object is to provide such a process which will result in filaments having improved. and more pronounced crimp.
The invention will be described annexed drawing, in which:
Fig. 1 is a general diagrammatic view of the employed in this invention;
Fig. 2 is a detailed side view of the extruding die and employed in this invention; and Fig. 3 is a sectional view along line 33 of Fig. 2.
SYNOPSIS OF THE INVENTION The above and other objects are secured,in accordance with this invention, in a process of the general type in connection with the apparatus substantial time to assume the kinked configuration.
"The more rapid relaxation and kinking obtained in accordance with this invention avoids the necessity for and space for the filaments while they are relaxing. Also the more rapid relaxation accordance with thisinvention results in a more pronounced and resilient kinking of the filaments;the delay in-relaxationincurred with solution of asurface-active agent is distributed upon the filaments at a point subsequent to the orientation of the filaments, and in which the manufacture e as Terylene or 2,875,019 iatented eb. 24, 19559 THE CRYSTALLINE RESINS The resins employed in the manufacture of kinked filamerits in accordance with this invention are of the special class known as crystalline resins. These resins are solid state, the long molecular chains of these resins tend to associate together locally to produce crystalline regions. If these resins are formed into filaments, as for instance by extrusion in the heat-softened state, and the filaments are thereafter subjected to stretching, these crystalline .aggregates become aligned lengthwise in the direction of stretching and impart a high degree of strength and flexibility to the resultant filaments. Resins of this type are well known, and include for'instance the vinylidene chloride resins, which are polymers of vinylidene chloride and copolymers thereof with up to 20% of other unsaturated compounds copolymerizable therewith, such for example, as vinyl chloride, vinyl fluoride, vinyl acetate, styrene, esters of acrylic and methacrylic acids such as methyl methacrylate, and ethyl methacrylate, acrylonitrile, vinyl typeethers and ketones such as methyl vinyl ether, methyl vinyl ketone and related compounds such as methyl isopropenyl ketone and the like. For a more complete list of compounds known to copolymerize with vinylidene chloride to produce crystalline resins which can be processed as described herein see Krczil "*Kurzes Idandbuch (ler Polymerisation Technik, vol. II, Mehrstoff Polymerization," Edwards Bros. Inc., page 739, the items indented under Vinyliden chlor'id." These vinylidene chloride resins are particularly adapted for use in this invention, and outstanding results have been obtained therewith. However, the invention is also applicable to the processing into curly crimped filaments of othercrystalline resins, such for instance as the nylon resins, which are high molecular weight condensation products of dicarboxylic acidswith diamines or of amino acids alone or of mixtures of amino acids with dicarboxylic acids and diarnines;
Dacron which are condensation prodnets of terephthalic acid and ethylene glycol; polyethylene; and polymers of 2,3-dichlorobutadiene-1,3 such as described in the patent to Kuhn 2,451,195. All of these resins maybe processed in accordance with this inventio-ninto crimped fibers having excellent curliness, loft andfeelz' i As noted hereinabove, it is known that kinked filaments of crystalline resins may be produced by melt-extruding extruded filaments, and quenching, orienting andrelaxingthe filaments. The process may take various forms; for instance, air maybe blown upon thefilaments from all sides as they emerge from the extrusion die. It is preferable, however, to blow the air upon one side only An advantageous means for achieving thispurpo'se consists in 'an arrangement in which theextruding dies have the orifices thereof arranged in a circle in a horizontal plane with the orifices opening downwardly, normal to the plane of said circle; Theemerging filaments are conducted vertically downwardly from said orifices, so that they form a substantially cylindrical array-i. e., at the orifice the filaments are all substantially parallel to.each other and equidistant from and substantially parallel to an axis drawn perpendicular with the center of the circle upon which the orifices of the die are disposed. This is best seenin the drawing,
which shows a conventional screw type extruding ma chine 10 which takes raw granular resin, melts it and forces it intoan extruding head'l Z: Asshown in Fig. 2,
aromatic polyester resins such this extruding head comprises a conical distributing passage 14 into which the molten resin is forced by the extruding machine 10, which receiving passage leads downward to the periphery of a die 16. The face of this die 16 is disposed in a horizontal plane and is provided with a large number of die orifices 18 communicating with the conical passage 14 from which they receive the molten resin under pressure and extrude it as filaments 20. These orifices are arranged in a circle having its center at the center 22 of the die 16, and it will be seen that the filaments 20 are extruded downwardly in a substantially vertical direction equidistant from an axis 24 drawn through the center 22 and perpendicular to the face of the die 16.
It will be understood that the description of the filaments 20 as being in a cylindrical array is approximate only: they will be deflected outwardly by cooling air as described below. 'Countervailing this, the filaments will usually also be drawn inwardly into a frusto-conical array, since they aregathered together in passing over the guides 26 in the quenching bath 28. For all practical purposes, however, the array of filaments may be designated cylindrical.
Means are provided for directing a flow of cooling air or other gas radially in all directions away from the axis of the cylindrical array of extruded filaments and outwardly past the extruded filaments. This flow of coolling air is indicated by the arrows 30. As shown, this means comprises an air jet 32 mounted upon a bracket arm 33 attached to the wall of a quenching tank into which the filaments ultimately fall. This air jet is directed upwardly and concentrically of the cylindrical array of filaments so as to project a stream ofair (indicated by the arrows 34) against a discoidal deflector plate 36 which is suspended from the extrusion die 16 in a position immediately below the die and coaxial of the cylindrical array of filaments. The air from the jet impinging upon this deflector plate is deflected radially outwardly and away from the axis24 of the cylindrical array of filaments in all directions past the freshly extruded filaments 20. This air flow effects two purposes; first it rapidly chills the skin surface of the filaments and does do in a non-uniform manner, the greatest cooling effect being on that side of any given filament facing the axis of the cylindrical array of filaments thereby setting up uneven strains in the filaments; likewise, the flow of air appears to induce vibrations in the freshly extruded filaments, setting up varying strains in the filaments distributed periodically lengthwise of the filaments.
The filaments after passing the outwardly-directed flow 30 of cooling air, drop into a tank 28 of cooling water 40. The filaments thereby become chilled and completely solidified, whereby the strains induced as above discussed become preserved therein. The filaments then pass down through the bath under a set of guide, pins 26 and thence upward through and out of the bath to and over a guide roll 41 to a pair of drawing rolls 42,.
The drawing rolls are driven at a peripheral speed in l excess of the linear velocity at which the filaments are extruded; due to the'resistance of the water 40 andto some extent the friction of the pins 26, a considerable tension is induced in the filaments and they are stretched to several times their extruded length during their passage through the bath and to the drawing rolls, whereby the filaments are drawn into an oriented crystalline form. The filaments pass from the drawing rolls 42 to a windup drum 44 upon which the filaments are accumulated as a skeina A revolving roll 43 dipping into a trough 45 containing asolution or emulsion 47 of a surface-active agent bears against the windup drum so as to apply a regulated amount of the surface-active agent to the filaments as they accumulate upon the drum. The surface-activeagent solution (or emulsion) may also be applied in a number of other ways. For example, a constant regulated stream may be applied from an overhead reservoir directly onto the filament as it is wound upon drum 44. Alternatively the solution rfiay be pumped from a reservoir and applied directly. In another modification the filament may pass over an applicator arrangement similar to the assembly 43, 45 prior to reaching drum 44. When a sufficiently large skein of filaments has accumulated on the drum, the filament is cut and transferred to a second windup roll 46 so as to be wound and accumulated upon the second windup roll. The accumulated fila ment is then stripped from the first winduproll. Immediately upon removal of the tension, the stripped filaments contract and, due to the uneven strains set up by the action of the air flow to which they were subjected between the extruder and the quenching bath, this contraction takes place with the formation of kinks and curls which are quite sharp and close. contrast to theresults obtained when the identical process is carried out without the application of the surface-active agentsolution 47;in such case the filaments must be hung up' in a relaxed condition for several hours in order to develop the kinks.
Reverting to the second windup drum 46, an applicator roll 49 similar to the applicator roll 43 bears against the windup drum and is arranged to apply the solution 47 of the wetting agent to the filaments as they accumulate on the drum. When a convenient amount of filament has accumulated upon the drum 46, the filament is again cut and transferred back to the first windup drum 44, and the accumulated filament stripped from the drum 46, and so on, the filament being accumulated alternately upon the two drums 46.
As to the surface-active agent applied by the rolls 43 and 49, this may be any of a wide variety of such materials. For instance the ordinary alkali metal and amine fatty acid soaps such as sodium laurate, sodium myristrate, sodium palmitate, potassium oleate, potassium stearate, triethanolamine stearate and the like may be employed. Likewise there may be employed sulfateand sulfonategroup-containing surface-active agents, such as the sulfonated fatty oils and fatty acids, anionic phosphated alcohols, the alkyl sulfosuccinates, the fatty alcohol sulfates. and the like, as exemplified in turkey red oil, sulfated castor oil fatty acids, sulfated coconut oil alco hol's, di-(Z-ethyl hexyl) sulfosuccinate, sodium dodecyl naphthalene sulfonates and the like. Other classes of surface-activeagents include the fatty amines and amides, such as dodecyl amine, hexadecyl amine, stearamide, N-stearyl methylolamide, and the like. In general, it appears thatthose surface-active agents which have the greatest antistatic action exert the most effective action in the practice of this invention, although there appears to be no apriori reason why this should be so. Surfaceactive agents in general may be defined as compounds containing from 8 to 22 carbon atoms coupled to highly polar solubilizing groups such as alkali metal and ammonium carboxylate groups, sulfate half-ester groups, sulfonate groups, phosphate partial ester groups, primary, secondary, tertiary and quaternary amine groups and the like. The surface-active agent is conveniently supplied to the applicator rolls as a 0.5 to 10% (preferably 2.0% solution in water, and a sufficient amount will .be used so that the filament takes up 0.01 to 3.0% (preferably l.()%) ofzsprface-active agent, based on the weight of the filament. v
A point which it is highly desirable to observe in the application of the surface-active agent to the filament is that it ,shall be Withhflld until after the orienting step, e. g. the cold stretching effected in advance of the drawing rolls 42. It has been found, for operational reasons, that the surface-active agents interfere with the colddrawing behavior of the filament, causing wrapping of broken filaments on rolls 42 and slippage of the main filament band resulting in uneven orienting stretch.
With the foregoing general discussion in mind, there This is in sharp "are given herewith detailed ation of the process of this are by weight.
aa zegore examples iof modes of operinvention. All parts :given Examples RESIN FORMULATION Parts Vinylidene chloride resin (a copolymer of 85% vinylidene chloride, 15% vinyl chloride) 92 Tertiary-butyl phenyl salicylate 5 Phenoxy propene oxide 2 SURFACE-ACTIVE AGENTS Two-percent aqueous solutions of each of the following:
Antistat N, an anionic phosphated alcohol mixture marketed by E. I. du Pont de Nemours and Co.
Olate flakes, a relatively pure, neutral sodium oleate marketed by Armour and Co.
Avitone A, a modified anionic sodium salt of su'lfonated hydrocarbon marketed 'by E. I. du Pont de Nemours & Co.
Polyethylene Glycol 400 Monolaurate, marketed by Kessler Chemical Co.
Zelec DP, a permanent antistat having an acrylic ester resin base, marketed by E. I. du Pont de Nemours & Co. v
G 1300, a polyoxyethylene sorbital marketed by Atlas Powder Company.
Profine, an anionic fatty ester based compound, marketed by Armour & Co.
Nacconol NR, a sodium alkyl aryl sulfonate, marketed by National Aniline Division, Allied Chemical & Dye Corporation.
v The ingredients listed under Resin Formulation were blended together and placed in the extruder of Figs. 1-3. A number of runs was made, using a different one of the surface-active agent solutions listed above in each of the several runs. Specifications and dimensions of the equipment, and operating conditions, were as follows:
EXTRUDING MACHINE Make: National Rubber Machinery Co.
Size: 2 inch Revolutions per minute of screw: 30-45 R. P. M. Temperature of barrel: 170 C.
Temperature of extruding head: 190 C.
EXTRUDING DIE 16 Number of orifices 18: 250
Diameter of orifices 18: 0.0125 inch Diameter of circle upon which the orifices are arranged: 6 inches Temperature of die 16: 170 C.
Through-put of resin through each die orifice: lb. per min.
Theoretical speed of filament extruded through orifice (assuming no contraction of diameter of filament): 132 ft. per min.
FLOW OF COOLING AIR Diameter of air jet orifice: /8 inch Volume of air to jet: 125 cubic ft. free air per min.
Distance from nozzle tip to deflector plate: s inch Approximate velocity of air flow outward past the filament at a point inch below die: 16 ft. persec.
QUENCHING, ORIENTATION AND TAKE-OFF PROPERTIES OF THE CURLY FILAMENT Diameter of individual filament: .0018 inch Tensile strength: 26,100 pounds per square inch Kinks in filament per inch of length of filament: 8
derivative,
'6 Approximate height of kinks from one extreme to other: .125 inch Elongation at break: 13%
The filaments in all runs relaxed immediately upon removal from the windup drums 44 and 46, and formed tight kinks and curls immediately. In comparable runs in which no surface-active material was applied, it was necessary to hang the'fiiarnents in a relaxed condition for from 1 to 24 hours in order to develop the optimum curl and kink in the filaments.
The filaments produced as above described 'had excellent feel, handle and loft'comparable to naturally kinked fibers such as wool, alpaca and the like. The filaments were spun into yarn which was woven as the pile of an Axminster carpet, and in this application exhibited a'very desirable loft and showed good resistance to ordinary wear. The filaments were likewise found highly suitable when spun into yarns for knitting into garments, and for ordinary woven fabric.
From the foregoing general discussion and detailed description of the operation of the invention, it will be evident that this invention provides a novel process and apparatus for the production of curly, kinked fine filaments of oriented crystalline resins. The process can be carried out With a minimum of skilled attendance and the apparatus required is both simple and inexpensive. The process avoids the necessity for providing a large detention space for hanging the filament to develop the curl thereof, which has heretofore been necessary in processes of the general type.
What is claimed is:
1. Process which comprises melt-extruding an array of filaments of an orientable crystalline thermoplastic resin, chilling the filaments when freshly extruded by blowing air thereupon, quenching said filaments in a cooling medium, subjecting the filaments to cold drawing in the absence of a surface-active agent, applying a surface-active agent to the filaments while still under tension, and thereafter removing tension from the filaments to permit them to relax into a crimped configuration, the surface-active agent applied to the filaments being a compound containing from 8 to 22 carbon atoms coupled to a highly polar solubilizing group selected from the group consisting of alkali metal carboxylate groups, ammonium carboxylate groups, sulfate half-ester groups, sulfonate groups, phosphate partial ester groups, primary amine groups, secondary amine groups, tertiary amine groups and quaternary amine groups.
2. Process which comprises melt-extruding an array of filaments of a vinylidene chloride resin, chilling the laments when freshly extruded by blowing air thereupon, quenching said filaments in a cooling medium, subjecting the filaments to cold drawing in the absence of a surface-active agent, Winding the cold-drawn filaments upon a collecting drum, applying a surface-active agent to the filaments while still under tension and wound upon said collecting drum, and stripping said filaments from said drum so as to remove tension from the filaments to permit them to relax into a crimped configuration, the surface-active agent applied to the filaments being a compound containing from 8 to 22 carbon atoms coupled to a highly polar solubilizing group selected from the group consisting of alkali metal carboxylate groups, ammonium carboxylate groups, sulfate half-ester groups, sulfonate groups, phosphate partial ester groups, primary amine groups, secondary amine groups, tertiary amine groups and quaternary amine groups.
3. Process which comprises melt-extruding an array of filaments of an orientable crystalline thermoplastic resin, chilling the filaments when freshly extruded by blowing air thereupon, quenching said filaments in a cooling medium, subjecting the filaments to cold drawing in the absence of a surface-active agent, winding the cold-drawn filaments upon a collecting drum, applying a phosphated alcohol surface-active agent containing from 8 to 22 carbon atoms to the filaments while still under tension and wound upon said collecting drum, and stripping said filaments from said drum so as to remove tension from the filaments to permit them to relax into a crimped configuration.
4. Process which comprises melt-extruding an array of filaments of an orientable crystalline thermoplastic resin, chilling the filaments when freshly extruded by blowing air thereupon, quenching said filaments in a cooling medium, subjecting'the filaments to cold drawing in the absence of a surface-active agent, winding the colddrawn filaments upon a collecting drum, applying an alkali metal soap containing from 8 to 22 carbon atoms to the filaments while still under tension and wound upon said collecting drum, and stripping said filaments from said drum so as to remove tension from the filaments to permit them to relax into a crimped configuration.
5. Process which comprises melt-extruding an array of filaments of a vinylidene chloride resin, chilling the filaments when freshly extruded by blowing air thereupon, quenching said filaments in a cooling medium, subjecting the filaments to cold drawing in the absence of a surface-active agent, windingthe cold-drawn filaments upon a collecting drum, applying a phosphated alcohol upon a collecting drum,
surface-active agent containing from 8 to 22 carbon atoms to the filaments while still under tension and wound upon said collecting drum, and stripping said filaments from said drum so as to remove tension from the filaments to permit them to relax into a crimped configuration.
6. Process which comprises melt-extruding an array of filaments of a vinylidene chloride resin, chilling the filaments when freshly extruded by blowing air thereupon, quenching said filaments in a cooling medium, subjecting the filaments to cold drawing in the absence of a surface-active agent, winding the cold-drawn filaments applying an alkali metal soap containing from 8 to 22 carbon atoms to the filaments while still under tension and wound upon said collecting drum, and stripping said filaments from said drum so as to remove tension from the filaments to permit them to relax into a crimped configuration.
References Cited in the file of this patent UNITEDSTATES PATENTS 2,287,099 Hardy et al. June 23, 1942 2,327,460 Rugeley Aug. 24, 1943 2,510,967 Flanagan June 13, 1950 2,730,758 Morrell et al. M Jan. 17, 1956
Claims (1)
1. PROCESS WHICH COMPRISES MELT-ETRUDING THERMOLASTIC OF FILAMENTS OF AN ORIENTABLE CRYSTALLIE THERMOPLWWTIC RESIN, CHILLING THE FILAMENTS WHEN FRESHLY EXTRUDED BY BLOWING AIR THEREUPON, QUENCHING SAID FILAMENTS IN A COOLING MEDIUM, SUBJECTING THE FILAMENTS TO COLD DRAWING IN THE ABSENCE OF A SURFACE-ACTIVE AGENT, APPLYING A SURFACE-ACTIVE AGENT TO THE FILAMENTS WHILE STILL UNDER TENSION AND THEREAFTER REMOVING TENSION FROM THE FILA MENTS TO PERMIT THEN TO RELAX INTO A CRIMPLED CONFIGURA TION, THE SURFACE-ACTIVE AGENT APPLIED TO THE FILAMENTS BEING A COMPOUND CONTAINING FROM 8 TO22 CARBON ATOMS COUPLED TO A HIGHLY POLAR SOLUBLIZING GROUP SELECTED FROM THE GROUP CONSISTING OF ALKALI METAL CARBOXYLATE GROUPS, AMMONIUM CARBOXYLATE GROUPS, SULFATE HALF-ESTER GROUPS, SULFONATE GROUP PHOSPHATE PARTIAL PARTIAL ESTER GROUPS PRIMARY AMINE GROUPS, SECONDARY AMINE GROUPS, TERTIARY AMINE GROUPS AND QUANTERNARY AMINE GROUPS.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US559709A US2875019A (en) | 1956-01-17 | 1956-01-17 | Method for producing crimped filaments |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US559709A US2875019A (en) | 1956-01-17 | 1956-01-17 | Method for producing crimped filaments |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2875019A true US2875019A (en) | 1959-02-24 |
Family
ID=24234694
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US559709A Expired - Lifetime US2875019A (en) | 1956-01-17 | 1956-01-17 | Method for producing crimped filaments |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2875019A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3039524A (en) * | 1958-11-03 | 1962-06-19 | Du Pont | Filaments having improved crimp characteristics and products containing same |
| US3418160A (en) * | 1965-05-14 | 1968-12-24 | Du Pont | Process for coating polyester fibers with a mixture of lanolin and an oily silicone |
| US3457340A (en) * | 1966-03-25 | 1969-07-22 | Du Pont | Process for uniform application of finish to polyester yarns |
| US3480709A (en) * | 1967-01-03 | 1969-11-25 | Hoechst Ag | Process for the manufacture of filaments of synthetic linear polymers of high molecular weight crimped during spinning |
| US4301102A (en) * | 1979-07-16 | 1981-11-17 | E. I. Du Pont De Nemours And Company | Self-crimping polyamide fibers |
| US4343860A (en) * | 1979-07-16 | 1982-08-10 | E. I. Du Pont De Nemours And Company | Self-crimping polyamide fibers |
| US4446089A (en) * | 1982-02-17 | 1984-05-01 | Basf Aktiengesellschaft | Process and apparatus for the production of plastic strands |
| US5785997A (en) * | 1993-10-22 | 1998-07-28 | Bayer Aktiengesellschaft | Continuous process for melt-spinning monofilaments |
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| US2287099A (en) * | 1937-02-15 | 1942-06-23 | Du Pont | Artificial wool |
| US2327460A (en) * | 1939-05-10 | 1943-08-24 | Carbide & Carbon Chem Corp | Process for stapling and crimping synthetic textile fibers |
| US2510967A (en) * | 1946-11-12 | 1950-06-13 | New Wrinkle Inc | Apparatus for producing wrinkle texture on nonwrinkling films |
| US2730758A (en) * | 1954-07-21 | 1956-01-17 | Firestone Tire & Rubber Co | Method and apparatus for the production of crimped filaments |
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- 1956-01-17 US US559709A patent/US2875019A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2287099A (en) * | 1937-02-15 | 1942-06-23 | Du Pont | Artificial wool |
| US2327460A (en) * | 1939-05-10 | 1943-08-24 | Carbide & Carbon Chem Corp | Process for stapling and crimping synthetic textile fibers |
| US2510967A (en) * | 1946-11-12 | 1950-06-13 | New Wrinkle Inc | Apparatus for producing wrinkle texture on nonwrinkling films |
| US2730758A (en) * | 1954-07-21 | 1956-01-17 | Firestone Tire & Rubber Co | Method and apparatus for the production of crimped filaments |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3039524A (en) * | 1958-11-03 | 1962-06-19 | Du Pont | Filaments having improved crimp characteristics and products containing same |
| US3418160A (en) * | 1965-05-14 | 1968-12-24 | Du Pont | Process for coating polyester fibers with a mixture of lanolin and an oily silicone |
| US3457340A (en) * | 1966-03-25 | 1969-07-22 | Du Pont | Process for uniform application of finish to polyester yarns |
| US3480709A (en) * | 1967-01-03 | 1969-11-25 | Hoechst Ag | Process for the manufacture of filaments of synthetic linear polymers of high molecular weight crimped during spinning |
| US4301102A (en) * | 1979-07-16 | 1981-11-17 | E. I. Du Pont De Nemours And Company | Self-crimping polyamide fibers |
| US4343860A (en) * | 1979-07-16 | 1982-08-10 | E. I. Du Pont De Nemours And Company | Self-crimping polyamide fibers |
| US4446089A (en) * | 1982-02-17 | 1984-05-01 | Basf Aktiengesellschaft | Process and apparatus for the production of plastic strands |
| US5785997A (en) * | 1993-10-22 | 1998-07-28 | Bayer Aktiengesellschaft | Continuous process for melt-spinning monofilaments |
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