EP0276756A2 - Conductive composite filaments and fibrous articles containing the same - Google Patents
Conductive composite filaments and fibrous articles containing the same Download PDFInfo
- Publication number
- EP0276756A2 EP0276756A2 EP88100844A EP88100844A EP0276756A2 EP 0276756 A2 EP0276756 A2 EP 0276756A2 EP 88100844 A EP88100844 A EP 88100844A EP 88100844 A EP88100844 A EP 88100844A EP 0276756 A2 EP0276756 A2 EP 0276756A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- conductive
- filament
- core
- sheath
- conductive path
- 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.)
- Granted
Links
- 239000002131 composite material Substances 0.000 title claims abstract description 49
- 239000002245 particle Substances 0.000 claims abstract description 51
- 239000000203 mixture Substances 0.000 claims abstract description 30
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 27
- 229920000642 polymer Polymers 0.000 claims description 25
- -1 polyethylene terephthalate Polymers 0.000 claims description 20
- 239000000835 fiber Substances 0.000 claims description 12
- 229920002292 Nylon 6 Polymers 0.000 claims description 8
- 239000004698 Polyethylene Substances 0.000 claims description 8
- 230000002093 peripheral effect Effects 0.000 claims description 6
- 229920000573 polyethylene Polymers 0.000 claims description 5
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 5
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 4
- 229930040373 Paraformaldehyde Natural products 0.000 claims description 3
- 239000004743 Polypropylene Substances 0.000 claims description 3
- 229920006324 polyoxymethylene Polymers 0.000 claims description 3
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 claims description 2
- 229920000299 Nylon 12 Polymers 0.000 claims description 2
- 229920000305 Nylon 6,10 Polymers 0.000 claims description 2
- 229920002302 Nylon 6,6 Polymers 0.000 claims description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 claims description 2
- 239000000306 component Substances 0.000 description 48
- 229910052751 metal Inorganic materials 0.000 description 28
- 239000002184 metal Substances 0.000 description 28
- 229920001940 conductive polymer Polymers 0.000 description 17
- 238000002156 mixing Methods 0.000 description 11
- 238000005299 abrasion Methods 0.000 description 10
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 10
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 9
- 238000009987 spinning Methods 0.000 description 9
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 8
- 229910044991 metal oxide Inorganic materials 0.000 description 8
- 150000004706 metal oxides Chemical class 0.000 description 8
- 229910001887 tin oxide Inorganic materials 0.000 description 8
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 239000004744 fabric Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000004677 Nylon Substances 0.000 description 5
- 229910000410 antimony oxide Inorganic materials 0.000 description 5
- 229920001778 nylon Polymers 0.000 description 5
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 5
- 229920000914 Metallic fiber Polymers 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000010954 inorganic particle Substances 0.000 description 4
- 238000009940 knitting Methods 0.000 description 4
- 238000010791 quenching Methods 0.000 description 4
- 230000000171 quenching effect Effects 0.000 description 4
- 230000003068 static effect Effects 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 238000009941 weaving Methods 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000003190 augmentative effect Effects 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000008358 core component Substances 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- 238000007599 discharging Methods 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000002923 metal particle Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000036555 skin type Effects 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000002238 attenuated effect Effects 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- CJOBVZJTOIVNNF-UHFFFAOYSA-N cadmium sulfide Chemical compound [Cd]=S CJOBVZJTOIVNNF-UHFFFAOYSA-N 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229920000547 conjugated polymer Polymers 0.000 description 1
- 230000001268 conjugating effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- BWFPGXWASODCHM-UHFFFAOYSA-N copper monosulfide Chemical compound [Cu]=S BWFPGXWASODCHM-UHFFFAOYSA-N 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 1
- GBRBMTNGQBKBQE-UHFFFAOYSA-L copper;diiodide Chemical compound I[Cu]I GBRBMTNGQBKBQE-UHFFFAOYSA-L 0.000 description 1
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 description 1
- 229940112669 cuprous oxide Drugs 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000005486 organic electrolyte Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
- 239000002491 polymer binding agent Substances 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910001930 tungsten oxide Inorganic materials 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05F—STATIC ELECTRICITY; NATURALLY-OCCURRING ELECTRICITY
- H05F3/00—Carrying-off electrostatic charges
- H05F3/04—Carrying-off electrostatic charges by means of spark gaps or other discharge devices
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/09—Addition of substances to the spinning solution or to the melt for making electroconductive or anti-static filaments
Definitions
- the present invention relates to novel conductive composite filaments, more particularly, conductive composite filaments which are industrially easily manufacturable, having substantially no metal abrasive property, and further relates to antistatic fibrous articles containing the same.
- fibers particularly, hydrophobic fibers consisting of polyester, polyamide, polyacrylonitrile, polyolefin or the like, generate a lot of static electricity due to friction, etc., often exceeding 10 kV, which causes various troubles. Therefore, many proposals relating to destaticization (imparting of antistatic properties) have been made.
- the metallic fibers have shortcomings, such as brittleness to induce breakages by bending during processing and using, which cause a decrease in antistatic property. Also the metallic fibers are difficult in blending, mixed weaving or mixed knitting with other fibers and, moreover, have an inherent metallic luster that impairs the quality of articles when the metallic fibers are incorporated therewith.
- metal deposited fibers and conductive material coated fibers also have many drawbacks, such as an extremely high cost of production, a low durability owing to liability to detachment of the coating by bending or due to friction during processing and using, or the like.
- conductive particles for example, carbon black, metal particles, etc.
- composite filaments in which a conductive component composed of a thermoplastic polymer containing conductive particles, for example, carbon black, metal particles, etc., dispersed therein and a non-conductive component of a fiber-forming thermoplastic polymer are bonded together in a side by side or sheath-core relationship uniformly extending along the longitudinal axis of the filament have been proposed in the gazettes of Japanese Patent Application Publication Nos. 31,450/77, 44,579/78 and 25,647/82, Japanese Patent Application Laid-open No. 60-224,813, etc.
- sheath-core type composite filaments those having a non-conductive component completely encapsulating a conductive particles containing conductive component, since dielectric breakdown in the sheath portion to induce corona discharge hardly occurs, have a shortcoming that is a poor antistatic property.
- these composite filaments exhibit noticeable black or dark grey color of carbon black or inorganic conductive particles, deteriorate the appearance of articles containing these filaments.
- these composite filaments having a hard conductive particles containing conductive component exposed on the filament surface when the filaments travel as rubbing upon a stationary body, abrade and eventually mar the body due to friction. Therefore, such composite filaments thus provided with an augmented metal abrasive property are involved in serious problems in the course of manufacturing and processing.
- the gazette of Japanese Patent Application Laid-open No. 60-110,920 discloses a core and thin skin type composite filament that comprises a skin component having the thinnest portions of 3 ⁇ m or less on the cross section.
- This filament is very excellent for obviating the metal abrasive property as well as providing the antistatic property.
- the non-conductive skin is made thin enough to provide a satisfactory antistatic property, the skin becomes liable to break, resulting in metal abrasion by the uncovered core. Accordingly, this type of filament still poses a problem such that stable manufacture is difficult to be performed.
- the gazette of Japanese Patent Application Laid-open No.60-224,812 discloses an improved core and thin skin type composite filament, where the skin is composed of a fiber-forming polymer having conductive particles of metal oxide or metal compound, and more preferably the particle size satisfies the formula; 0.5 ⁇ size of conductive particle/minimum thickness of skin ⁇ 4.
- the conductive particles in the skin are contained much enough to provide a satisfactory antistatic property, the color or metal abrasion is revealed again.
- a conductive composite filament prepared by conjugating a mixture (A) consisting of a conductive polymer composition (P1 ⁇ ) and a fiber-forming thermoplastic polymer (P2) which is incompatible with (P1 ⁇ ) with non-conductive fiber-forming thermoplastic polymer.
- the mixture (A) occupies part of the surface area of the filament and part of (P1 ⁇ ) comes up to the surface in the lengthwise direction of the filament through an opening.
- a conductive composite filament in fact, is unstable in yarn-spinnability and, moreover, insufficient in electroconductivity for lack of a conductive core as in the Case of Comparative Example Y17 that will be described hereinafter.
- An object of the present invention is to provide improved conductive composite filaments which have high whiteness, excellent antistatic property, exhibiting no abrasive property, which can be commercially easily manufactured.
- Another object of the present invention is to provide fibrous articles with excellent antistatic property and aesthetic appearance which contain the conductive composite filaments of the invention.
- a unitary conductive composite filament which comprises:
- the cross-sectional figure of the composite filaments according to the present invention is not specifically limited. It may be either circular or non-circular, but the circular one is preferred.
- the cross-sectional figure of the conductive component is important.
- the cross-sectional figure of the conductive component consists of a thick conductive core 1 and a thin conductive path 2, both lapped in a sheath 3 composed of a non-conductive component extending along the entire length of the filament.
- the conductive path 2 extends laterally from a part of the periphery of the thick conductive core 1, transversely through the sheath 3, up to or close to the outer circumference of the sheath. Longitudinally, it extends along the entire length of said core in such a manner that the conductive path is exposed at least partly lengthwise and not more than 1.5 ⁇ m in width on the outer peripheral surface of the sheath.
- a tadpole-like figure is particularly preferred which is composed of the conductive core as its head and the conductive path as its tail.
- the conductive core embedded in the sheath is positioned nearly in the center of the filament and only the tip of the conductive path barely reaches the circumference of the filament.
- the cross-sectional figure of the conductive component may be either same or different throughout the entire length of the filament.
- the figure or width of the conductive path may vary gradually along the longitudinal axis of the filament. This means that the thick conductive core extends continuously along the length of the filament and the thin conductive path can be exposed either continuously or intermittently lengthwise on the surface of the filament.
- the cross-sectional figure of the conductive core may be arbitrarily selected from circular, elliptical, triangular, rectangular or the like.
- the conductive core occupies a major portion, for example, at least 60% by volume, of the conductive component. Its thickness, for example, d1 in FIG. 1, is preferably at least 5 ⁇ m. There may be either case where the core is clearly distinguishable (e.g., FIG. 1) or indistinguishable (e.g., FIGS. 2 and 5).
- the conductive path means a thin portion conjoined with the conductive core. Its cross-sectional figure may be straight and, however, a bent or crooked one is more preferred for narrowing the exposed width of its tip. Additionally, from the joint with the conductive core to the tip, of the conductive path, the thicknesses may be substantially same (FIG. 1) and, however, those gradually attenuated (FIGS. 2, 4 and 5) or thin-and-thick (FIG. 6) are preferred for controlling the exposed width narrow as desired. In contrast, when the conductive component consists solely of a thin band without having a core (thick portion) as shown in FIG. 10, the electric conductivity or antistatic property is apt to decrease or become unstable, while, if it is formed thick, the metal abrasive property will increase appreciably, so that this type of the conductive component is not suitable.
- the width of the conductive path that is exposed on surfaces of the filament is not more than 1.5 ⁇ m, preferably not more than 1.2 ⁇ m, most preferably not more than 1.0 ⁇ m. If the exposed width is too large, the metal abrasion becomes liable to occur.
- the conductive path may be exposed lengthwise intermittently on the surface of the filament.
- the portion to be exposed is the tip or a part of its vicinity of the conductive path.
- the length along the longitudinal axis of the filament of the exposed portion is not specifically defined.
- the proportion of the exposed length to the entire length of the filament is preferably not more than 90%, more preferably not more than 70%, most preferably not more than 50%. Too large the width or the length proportion of the exposed portion tends to cause metal abrasion.
- the composite filaments according to the present invention have a novel crosssectional figure that is quite different from those of any conventional sheath-core or side by side type conductive composite filaments.
- the conjugate ratio that is, the area ratio occupied by the conductive component in the cross-section of the composite filaments is preferably 3-40%, more preferably 4-20%, most preferably 5-15%.
- the conjugate ratio is too small, the conductivity will decrease, lessening therefore the antistatic property.
- it is too large physical or mechanical properties of the filaments will be deteriorated and the metal abrasive property will be augmented.
- any kind of particles can be employed insofar as they have a specific resistance in powdery form of not more than about 104 ⁇ cm. Not only those particles coated with a metal oxide or metal hydroxide having high whiteness but also metallic powders (e.g., silver, nickel, copper, iron, alloys thereof, etc.) and metallic compounds such as copper sulphide, copper iodide, zinc sulphide, cadmium sulphide and the like, can be employed.
- metallic powders e.g., silver, nickel, copper, iron, alloys thereof, etc.
- metallic compounds such as copper sulphide, copper iodide, zinc sulphide, cadmium sulphide and the like.
- metal oxide particles mention may be made of particles of tin oxide, zinc oxide, copper oxide, cuprous oxide, indium oxide, zirconium oxide, tungsten oxide, etc. Most metal oxides are insulators or semi-conductors and do not show enough conductivity to satisfy the object of the present invention. However, the conductivity is increased, for example, by adding a small amount (not more than 50%, particularly not more than 25%) of a proper secondary component (impurity) to the metal oxide, whereby conductive metal oxide powders having sufficient conductivity to satisfy the object of the present invention can be obtained.
- a secondary component i.e., a conductivity modifier
- antimony oxide can be used for tin oxide, and also oxides of aluminum, gallium, indium, germanium, tin and the like for zinc oxide.
- particles wherein a conductive film of the above-described metal oxides or other metallic compounds is formed on surfaces of non-conductive inorganic particles such as titanium oxide, zinc oxide, magnesium oxide, tin oxide, iron oxide, silicon oxide, aluminum oxide and the like, also can be used.
- non-conductive inorganic particles such as titanium oxide, zinc oxide, magnesium oxide, tin oxide, iron oxide, silicon oxide, aluminum oxide and the like.
- conductive particles which is obtained by mixing tin-oxide-coated titanium oxide particles with antimony oxide and firing the resulting mixture.
- the conductivity of the conductive metal oxide particles is preferred to be not more than about 104 ⁇ cm, particularly not more than about 102 ⁇ cm, most preferably not more than about 101 ⁇ cm in specific resistance in the powdery state.
- the particles having about 102 ⁇ cm ⁇ 10 ⁇ 2 ⁇ cm are obtained and can be suitably applied to the object of the present invention.
- the particles more excellent in conductivity are more preferable.
- the specific resistance (volume resistivity) is measured by charging 5 g of a sample into an insulative cylinder having a diameter of 1 cm and applying a pressure of 200 kg to the cylinder from the top by means of a piston and applying a direct current voltage (for example, 0.001-1,000 V, current of 1 mA or less).
- the conductive particles are preferred to be sufficiently small in the grain size.
- Particles having an average grain size of 1-2 m can be used but, in general, those having an average grain size of not more than 1 ⁇ m, particularly not more than 0.5 ⁇ m, most preferably not more than 0.3 ⁇ m, are suitably used.
- the mixed ratio of the conductive particles in the conductive component depends upon the kind, conductivity, grain size, chain forming ability of particles, and the property, crystallinity, etc. of the polymer binder the particles are mixed with. However, it is generally within a range of about 10-85%, preferably about 20-80%, by weight.
- the mixed ratio of titanium oxide particles coated with a conductive film is generally in the range of about 40-85%, more preferably 50-80%, most preferably 60-80%, by weight.
- thermoplastic polymer to be mixed with the inorganic conductive particles, which forms the conductive component is not particularly limited and can be selected arbitrarily from a host of thermoplastic polymers such as polyamides, polyesters, polyolefins, polyvinyls, polyethers and the like. These polymers are preferred to have fiber-formability from the standpoint of spinning operation. However, even though those polymers deficient in fiber-formability are used, composite filaments can be provided with sufficiently good spinnability by using a fiber-forming thermoplastic polymer as the non-conductive component to be conjugated therewith.
- thermoplastic polymers used for the conductive component particularly preferred are those having a crystallinity of at least 60%, which are poor in compatibility with the non-conductive fiber-forming thermoplastic polymers.
- Such polymers include polyethylene, polypropylene, polyoxymethylene, polyethylene oxide and its derivatives (for example, ethylene oxide/ethylene terephthalate block copolymers), polyvinyl alcohol, polypivalolactone, polycaprolactone, etc.
- polyethylene, polypropylene polyoxymethylene, and copolymers thereof are particularly suitable.
- the conductive component is preferred to have a specific resistance (volume resistivity) of less than 107 ⁇ cm, more preferably not more than 104 ⁇ cm, and not more than 102 ⁇ cm is particularly preferred.
- dispersants for example, waxes, polyalkylene oxides, various surfactants, organic electrolytes, etc.
- coloring agents for example, waxes, polyalkylene oxides, various surfactants, organic electrolytes, etc.
- coloring agents for example, pigments, stabilizers (antioxidants, ultraviolet ray absorbents, etc.) flow improvers and other additives.
- any spinnable polymers can be used.
- spinnable polymers polyamides such as nylon-6, nylon-66, nylon-12, nylon-610 and the like, polyesters such as polyethylene terephthalate, polyethylene oxybenzoate, polybutylene terephthalate and the like, polyacrylonitrile and copolymers and modified polymers thereof, are particularly suitable.
- additives such as delustrants, pigments, coloring agents, stabilizers, antistatic agents (such as polyalkylene oxides, various surfactants or the like).
- the non conductive component composed of a fiber-forming thermoplastic polymer as described above is preferred to have a specific resistance of at least 107 ⁇ cm.
- the conductive core and conductive path usually have substantially the same composition.
- the thermoplastic polymer composition in the conductive path consists of a mixture of the polymer for the non-conductive sheath component with the polymer composition for the conductive core component.
- the mixing ratio of the both components is not specifically limited.
- a mixing ratio such as to bring the content in the mixture of the conductive inorganic particles into the range of 3-50%, particularly 5-40%, by weight, is preferred. If the content is too large, the composite filaments too much increase in metal abrasive property, while, if too small, the antistatic property becomes insufficient.
- the mixture is preferred to occupy at least the exposed portion on filament surfaces of the conductive path.
- the above-described polymer mixture can be produced according to any known processes.
- a process for mixing by means of a static mixer composed of relatively a few, preferably 1-3 mixing elements which is provided in a polymer flow path inside a spinneret assembly (FIG. 12), a mechanical mixer such as an impeller or rotor (FIG. 13), a hydrodynamic mixing utilizing collision of fluids caused by high pressure injection or a breaker such as glass beads or a filter layer provided in the flow path (FIG. 14), etc., and combinations thereof.
- a static mixer composed of relatively a few, preferably 1-3 mixing elements which is provided in a polymer flow path inside a spinneret assembly (FIG. 12), a mechanical mixer such as an impeller or rotor (FIG. 13), a hydrodynamic mixing utilizing collision of fluids caused by high pressure injection or a breaker such as glass beads or a filter layer provided in the flow path (FIG. 14), etc., and combinations thereof.
- the numeral 101 denotes an entrance for a fiber-forming thermoplastic polymer; 102, an entrance for a conductive component polymer composition; 103, a static mixer; 104, a kneader; 105, a mixing zone; 106-108, meeting points; 109, a constriction device, and 110, a spinneret.
- the fiber-forming thermoplastic polymer and conductive component polymer composition to be mixed with each other are preferred to be mutually incompatible. Such a combination provides a mixture in a mutually phase-separated state.
- an unevenly mixed state for example, a fine archipelagic or multi-layeredly dispersed state is preferred from the viewpoint of corona discharging.
- the thick conductive core for example, having a thickness of not less than 5 ⁇ m and a specific resistance of not more than about 107 ⁇ cm, extending continuously along the entire length of the filament, is considered to make movements in the longitudinal direction of the electric charge easy.
- This function since the conductive core has a thickness larger than a certain degree, will not be deteriorated in processes such as drawing, false-twisting, rewinding, knitting, weaving and the like.
- the conductive path conjoined with the thick conductive core reaches its tip up to or close to the surface of the filament and is exposed lengthwise continuously or intermittently, when the filaments are electrified, destaticization by corona discharge is considered to occur at a low potential.
- composite filaments of the present invention in a very small amount, fibrous articles provided with an excellent antistatic property can be produced without impairing aesthetic appearance, such as apparels, lingerie, foundations, hosiery, particularly working clothes for clean rooms, sheetings, carpets, upholsteries, interior cloths, or the like.
- the composite filaments of the invention may be mixed with other natural fibers or artificial fibers and used as continuous filament yarns, staple fibers, in a non-crimped, crimped, undrawn or drawn form.
- the antistatic property was evaluated according to the following method.
- An ordinary nylon-6 drawn yarn (210 deniers/54 filaments) was knit on a circular knitting machine, incorporating a conductive composite filament yarn in every eleventh course, to prepare a tubular knitted fabric mixed with 0.85% based on the weight of the fabric of the conductive composite filaments.
- the resulting fabric in which oils were removed by scouring was thoroughly washed with water, then dried at 80°C for 3 hours and further conditioned at 25°C in an atmosphere of 30% R.H. for 6 hours. Thereafter, the fabric was rubbed 15 times with a cotton cloth at the same temperature and humidity as the above, and the electrified charge after 10 seconds was measured.
- the metal abrasive property was measured by the time required for breaking a stainless steel wire having a diameter of 35 ⁇ m, when the filament yarn traveled on the stainless steel wire at a speed of 100 m/min. (The yarn tension before contacting was 4-5 g and the contact angle was 45°).
- the electric resistance was measured of a yarn consisting of 5 single filaments having a length of 10 cm. Both ends of the yarn were bonded to metal terminals with a conductive adhesive (Dodite D-550, manufactured by Fujikura Kasei K.K.), 10 V of direct current was applied between both the terminals, and the electric resistance was determined. The specific resistance of the conductive component was calculated from the above obtained value of the filament yarn.
- a conductive adhesive Dodite D-550, manufactured by Fujikura Kasei K.K.
- Conductive particles having an average grain size of 0.25 ⁇ m and a specific resistance of 6.3 ⁇ cm was obtained by firing a mixture of titanium oxide particles coated with a tin oxide film and 0.75% by weight of said particles of antimony oxide. Seventyfive parts by weight of the above obtained particles and 25 parts by weight of polyethylene having a molecular weight of 80,000 were kneaded together to prepare a conductive polymer composition A1.
- H2SO4 of 2.3 were simultaneously spun from orifices having a diameter of 0.25 mm at a spinning temperature of 280°C into composite filament yarns having cross-sectional figures as shown in Table 1, with a conjugated ratio of 1/9 (areal raio in cross section).
- the as-spun yarns were taken up on a bobbin at a rate of 800 m/min., while cooling and oiling. Then the taken-up filament yarns were drawn at a draw ratio of 2.6 times on a hot roll at 80°C, further contacting with a plate heater at 170°C, to produce drawn yarns Y1 ⁇ Y5 of 20 deniers/3 filaments which were wound up on a pirn.
- any of the yarns Y1 ⁇ Y5 had a specific resistance of not more than the order of 103 ⁇ cm and exhibited good conductivity.
- the yarns Y1 ⁇ Y3 and Y5 had good antistatic properties but the yarn Y4 that had not exposed the conductive polymer component on the filament surface was poor in antistatic property.
- the yarns Y1 ⁇ Y4 had a little metal abrasive property but the yarn Y5 exposing the conductive component largely in width on the surface of the filament had an extremely increased metal abrasive property.
- the yarn Y5 could not be stably manufactured due to increased abrasion of thread guides.
- the yarns Y1 ⁇ Y4 were respectively plied with a nylon-6 filament yarn of 2,600 deniers/140 filaments and the plied yarns were crimped by texturizing.
- a tufted carpet (looped, the mixed ratio of the conductive filaments: 0.17%) was produced.
- the charged voltages of the carpets incorporated with the yarns Y1 ⁇ Y3 of the present invention were -2.0 kV, -2.3 kV and -1.8 kV, respectively.
- that of the carpet incorporated with the yarn Y4 a sheath-core type composite filament yarn, was -4.3 kV and an electric shock was received from a grounded doorknob.
- the charged voltage of human body of a carpet composed only of nylon was measured -9.2 kV and the electric shock received from the grounded doorknob was so violent that a considerable fear was felt.
- a polyethylene terephthalate polymer having a molecular weight of 15,000 blended with 0.65% based on the weight of the polymer of titanium oxide as a delustrant was used as a non-conductive polymer and the conductive polymer composition A1 prepared in EXAMPLE 1 was used as a conductive polymer composition.
- These polymers were conjugated, in a spinneret, in side by side relation having a cross-sectional figure as shown in FIG. 3, and spun from orifices having a diameter of 0.3 mm at a spinning temperature of 285°C. After quenching and oiling, the as-spun filament yarn was wound up on a take-up roll at a rate of 1,000 m/min.
- Titanium oxide particles coated with tin oxide (SnO2) and 1.5% based on the weight of the particles of antimony oxide were mixed together and fired to produce oonductive particles having an average grain size of 0.25 ⁇ m, a content of tin oxide of 15% by weight, a specific resistance of 7 ⁇ cm and a whiteness, i.e., light reflection, of 83%.
- Seventy five parts by weight of the produced conductive particles and 25 parts by weight of a low density polyethylene having a molecular weight of about 50,000 and a melting point of 103°C were mixed and kneaded uniformly together with 0.5 parts by weight of magnesium stearate (a flow improver) to prepare a conductive polymer composition that was denoted as A2.
- Nylon-6 having a molecular weight of about 16,000 and a melting point of 215°C admixed with 0.8% based on the weight of the nylon of titanium oxide to prepare a polymer B1.
- the conductive polymer A2 and the polymer B1 were conjugate-spun with a conjugate ratio of 9/1 at a spinning temperature of 280°C from orifices having a diameter of 0.25 mm into composite filaments having cross-sectional figures as shown in Table 3.
- the as-spun filament yarns were wound up on a take-up roll at a rate of 800 m/min., while quenching and oiling. Then the yarns were drawn 2.6 times their original lengths with a hot roll at 80°C, further brought into contact with a plate heater at 170°C, and wound up on a pirn. Thus, drawn yarns Y10 ⁇ Y13 of 18 deniers/1 filament were obtained.
- any Of the yarns Y10 ⁇ Y13 had a specific resistance of the order of 103 ⁇ Cm and exhibited good conductivity.
- the yarns Y10 ⁇ Y12 had a good antistatic property of not more than 2.0 kV, but the yarn Y11 whose conductive polymer component was not exposed on the surface of the filaments had a poor antistatic property. Further, the yarns Y10 and Y11 had a decreased metal abrasive property, while the yarns Y12 and Y13 showed a considerably increased metal abrasive property.
- the yarns Y12 and Y13 abraded travellers so remarkably during draw-twisting operation that the stable manufacture of the yarns could not be performed.
- the yarn Y10 was the only yarn that had a good antistatic property as well as a decreased metal abrasive property.
- Titanium oxide particles coated with tin oxide and 0.75% based on the weight of the particles of antimony oxide were mixed together and fired to produce conductive particles having an average grain size of 0.25 ⁇ m and a specific resistance of 6.3 ⁇ cm.
- Seventyfive parts by weight of the produced conductive particles and 25 parts by weight of a polyethylene having a molecular weight of 80,000 were mixed and kneaded together to prepare a conductive polymer composition A3.
- a spinning machine provided with a static mixer comprising a couple of mixing elements in a spinneret assembly such as shown in FIG. 12, 10 parts by volume of the above conductive polymer A3 and 90 parts by volume of a nylon-6 (N1) having a relative viscosity in 95% conc. H2SO4 of 2.3 were spun from orifices having a diameter of 0.25 mm at a spinning temperature of 280°C to form filaments with cross-sectional figures and mixing ratios as shown in Table 5.
- the polymers N1 and A3 were introduced from the entrances 101 and 102, respectively, and the constriction devices 109 were adjusted to control the mixing ratio.
- the as-spun filament yarns were wound up on a take-up roll at a rate of 800 m/min., while quenching and oiling. Then the yarns were drawn 2.6 times their original lengths with a hot roll at 80°C, further brought into contact with a plate heated at 170°C, and wound up on a pirn. Thus, drawn yarns Y18 ⁇ Y20 of deniers/3 filaments were obtained.
- any of the yarns Y18 ⁇ Y20 had a specific resistance of the order of 102 ⁇ cm and exhibited good conductivity.
- the yarns Y18 and Y20 had a good antistatic property but the yarn Y19 whose conductive polymer component was not exposed on the surface of the filaments had a poor antistatic property.
- the yarns Y18 and Y19 had a decreased metal abrasive property, while the yarn Y20 showed a considerably increased metal abrasive property and could not manufactured stably due to abrasion of thread guides.
- the yarns Y18 and Y19 were respectively plied with a nylon-6 yarn of 2,600 deniers/140 filaments and the plied yarns were crimped by texturizing.
- a tufted carpet (looped, the mixed ratio of the conductive filaments: 0.17%) was produced.
- a charged voltage of a human body generated when a man putting on leather shoes walked on resulting carpet in a room at 25°C with 20% R.H. was measured.
- the charged voltage of the carpet incorporated with the yarn Y18 of the present invention was -2.1 kV.
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Abstract
Description
- The present invention relates to novel conductive composite filaments, more particularly, conductive composite filaments which are industrially easily manufacturable, having substantially no metal abrasive property, and further relates to antistatic fibrous articles containing the same.
- It is well known that fibers, particularly, hydrophobic fibers consisting of polyester, polyamide, polyacrylonitrile, polyolefin or the like, generate a lot of static electricity due to friction, etc., often exceeding 10 kV, which causes various troubles. Therefore, many proposals relating to destaticization (imparting of antistatic properties) have been made.
- One of them is a process to blend electrifiable fibers with metallic fibers. However, the metallic fibers have shortcomings, such as brittleness to induce breakages by bending during processing and using, which cause a decrease in antistatic property. Also the metallic fibers are difficult in blending, mixed weaving or mixed knitting with other fibers and, moreover, have an inherent metallic luster that impairs the quality of articles when the metallic fibers are incorporated therewith.
- Alternatively, metal deposited fibers and conductive material coated fibers also have many drawbacks, such as an extremely high cost of production, a low durability owing to liability to detachment of the coating by bending or due to friction during processing and using, or the like.
- Meanwhile, fibers composed of a thermoplastic polymer that contains conductive particles, for example, carbon black, metal particles, etc., dispersed therein, when the conductive particles are dispersed in an amount large enough to provide a conductivity, cannot avoid decreases in spinnability, tenacity and elongation. Consequently, it is extremely difficult to obtain practicable such fibers.
- In order to obviate such drawbacks, composite filaments in which a conductive component composed of a thermoplastic polymer containing conductive particles, for example, carbon black, metal particles, etc., dispersed therein and a non-conductive component of a fiber-forming thermoplastic polymer are bonded together in a side by side or sheath-core relationship uniformly extending along the longitudinal axis of the filament have been proposed in the gazettes of Japanese Patent Application Publication Nos. 31,450/77, 44,579/78 and 25,647/82, Japanese Patent Application Laid-open No. 60-224,813, etc.
- Among the above proposed sheath-core type composite filaments, those having a non-conductive component completely encapsulating a conductive particles containing conductive component, since dielectric breakdown in the sheath portion to induce corona discharge hardly occurs, have a shortcoming that is a poor antistatic property. In contrast, sheath-core type composite filaments, different therefrom, having a sheath composed of a conductive component as well as side by side type composite filaments wherein a conductive component and a non conductive component are bonded together in a side by side relationship, since the conductive component is exposed on the filament surface, are excellent in corona discharging property, i.e., antistatic property. However, these composite filaments exhibit noticeable black or dark grey color of carbon black or inorganic conductive particles, deteriorate the appearance of articles containing these filaments. Moreover, these composite filaments having a hard conductive particles containing conductive component exposed on the filament surface, when the filaments travel as rubbing upon a stationary body, abrade and eventually mar the body due to friction. Therefore, such composite filaments thus provided with an augmented metal abrasive property are involved in serious problems in the course of manufacturing and processing.
- In order to solve such problems, some proposals have been made. For example, the gazette of Japanese Patent Application Laid-open No. 60-110,920 discloses a core and thin skin type composite filament that comprises a skin component having the thinnest portions of 3 µm or less on the cross section. This filament is very excellent for obviating the metal abrasive property as well as providing the antistatic property. However, if the non-conductive skin is made thin enough to provide a satisfactory antistatic property, the skin becomes liable to break, resulting in metal abrasion by the uncovered core. Accordingly, this type of filament still poses a problem such that stable manufacture is difficult to be performed. The gazette of Japanese Patent Application Laid-open No.60-224,812 discloses an improved core and thin skin type composite filament, where the skin is composed of a fiber-forming polymer having conductive particles of metal oxide or metal compound, and more preferably the particle size satisfies the formula; 0.5≦ size of conductive particle/minimum thickness of skin ≦4. However, if the conductive particles in the skin are contained much enough to provide a satisfactory antistatic property, the color or metal abrasion is revealed again.
- Further, in order to mitigate the metal abrasion during manufacturing and processing of composite filaments, for example, of side by side type or the like that expose a conductive component on surfaces of the filament, there is disclosed, for example, in Japanese Patent Application Laid-open No. 61-132,626 a sheathcore type composite filament of which the sheath component is composed of a solvent soluble polymer. The sheath component of this filament can be removed by dissolving, after fabricated into articles, to expose the conductive core component. In the gazette of Japanese Patent Application Laid-open No. 61-152,823, there is also disclosed a conductive composite filament prepared by conjugating a mixture (A) consisting of a conductive polymer composition (P1ʹ) and a fiber-forming thermoplastic polymer (P2) which is incompatible with (P1ʹ) with non-conductive fiber-forming thermoplastic polymer. In this filament, the mixture (A) occupies part of the surface area of the filament and part of (P1ʹ) comes up to the surface in the lengthwise direction of the filament through an opening. However, such a conductive composite filament, in fact, is unstable in yarn-spinnability and, moreover, insufficient in electroconductivity for lack of a conductive core as in the Case of Comparative Example Y₁₇ that will be described hereinafter. Accordingly, fibrous articles containing such a filament are deficient in antistatic property and less practical. In the Japanese Patent Application Laid-open No. 57-161,126, there is also disclosed a composite filament whose exposed conductive component occupies 30% or less of the surface of the filament. Although both of these filaments have an excellent antistatic property and, in addition, careful consideration has been given to prevent the metal abrasion in manufacturing and processing steps, these filaments inconveniently necessitates use of special polymers or complicated apparatuses or imposition of extraordinarily delicate conditions for manufacture.
- An object of the present invention is to provide improved conductive composite filaments which have high whiteness, excellent antistatic property, exhibiting no abrasive property, which can be commercially easily manufactured.
- Another object of the present invention is to provide fibrous articles with excellent antistatic property and aesthetic appearance which contain the conductive composite filaments of the invention.
- The above objects of the present invention will be achieved by a unitary conductive composite filament which comprises:
- (a) a non-conductive component composed of a fiber-forming thermoplastic polymer, forming a sheath extending along the entire length of the filament, and
- (b) a conductive component consisting of a conductive core and a conductive path, being lapped in and extending lengthwise along said sheath, said conductive core being composed of a mixture of a thermoplastic polymer with inorganic particles, said conductive path having a composition the same as or different from the conductive core, comprising a thermoplastic polymer and inorganic conductive particles,
which is characterized in that said conductive path extends laterally from a part of the periphery of said conductive core, transversely through the sheath, up to or close to the outer circumference of the sheath and that the conductive path is exposed at least partly lengthwise and not more than 1.5 µm in width on the outer peripheral surface of the sheath. - For better understanding of the invention, reference is made to the accompanying drawings, wherein:
- FIGS. 1-6 show the cross-sectional views of the conductive composite filaments of the present invention;
- FIGS. 7-11 show the cross-sectional views of the conventional conductive composite filaments, FIG. 7 of a sheath core type and FIGS. 8-11 of side by side type filaments;
- FIGS. 12-14 are polymer flow diagrams in a spinneret assembly to be preferably employed for manufactur ing the filaments according to the present invention;
- FIG. 15 is a graph showing the relation between the blend ratio of the conductive composite filaments and the amount of the electrified charge in an example of the fibrous article, a nonwoven fabric composed of polyethylene terephthalate staple fibers, of the present invention;
- FIG. 16 is a graph showing the relation between the pitch of the conductive composite filaments spacedly incorporated into a fibrous article, i.e., a circular knitted fabric, and the voltage of frictional electrification;
- FIGS. 17 and 18 are SEM photomicrographs showing the cross-sectional view and side surface view, respectively, of the conductive composite filaments of the present invention (undrawn filaments); and,
- FIG. 19 is a SEM photomicrograph showing the cross-sectional and peripheral views of an example, the conductive composite filament Y₃, of the invention (the PE composing a conductive component has been removed from the undrawn filament).
- The cross-sectional figure of the composite filaments according to the present invention is not specifically limited. It may be either circular or non-circular, but the circular one is preferred.
- In the composite filaments of the present invention, the cross-sectional figure of the conductive component is important. As is shown in FIGS. 1-6, the cross-sectional figure of the conductive component consists of a thick conductive core 1 and a thin
conductive path 2, both lapped in asheath 3 composed of a non-conductive component extending along the entire length of the filament. Theconductive path 2 extends laterally from a part of the periphery of the thick conductive core 1, transversely through thesheath 3, up to or close to the outer circumference of the sheath. Longitudinally, it extends along the entire length of said core in such a manner that the conductive path is exposed at least partly lengthwise and not more than 1.5 µm in width on the outer peripheral surface of the sheath. - For the conductive component, a tadpole-like figure is particularly preferred which is composed of the conductive core as its head and the conductive path as its tail. With respect to the position of the conductive component in the cross-section of the filament, it is preferred that the conductive core embedded in the sheath is positioned nearly in the center of the filament and only the tip of the conductive path barely reaches the circumference of the filament.
- The cross-sectional figure of the conductive component may be either same or different throughout the entire length of the filament. In particular, the figure or width of the conductive path may vary gradually along the longitudinal axis of the filament. This means that the thick conductive core extends continuously along the length of the filament and the thin conductive path can be exposed either continuously or intermittently lengthwise on the surface of the filament.
- The cross-sectional figure of the conductive core may be arbitrarily selected from circular, elliptical, triangular, rectangular or the like. The conductive core occupies a major portion, for example, at least 60% by volume, of the conductive component. Its thickness, for example, d₁ in FIG. 1, is preferably at least 5 µm. There may be either case where the core is clearly distinguishable (e.g., FIG. 1) or indistinguishable (e.g., FIGS. 2 and 5).
- The conductive path means a thin portion conjoined with the conductive core. Its cross-sectional figure may be straight and, however, a bent or crooked one is more preferred for narrowing the exposed width of its tip. Additionally, from the joint with the conductive core to the tip, of the conductive path, the thicknesses may be substantially same (FIG. 1) and, however, those gradually attenuated (FIGS. 2, 4 and 5) or thin-and-thick (FIG. 6) are preferred for controlling the exposed width narrow as desired. In contrast, when the conductive component consists solely of a thin band without having a core (thick portion) as shown in FIG. 10, the electric conductivity or antistatic property is apt to decrease or become unstable, while, if it is formed thick, the metal abrasive property will increase appreciably, so that this type of the conductive component is not suitable.
- The width of the conductive path that is exposed on surfaces of the filament (e.g., d₂ in FIG. 1) is not more than 1.5 µm, preferably not more than 1.2 µm, most preferably not more than 1.0 µm. If the exposed width is too large, the metal abrasion becomes liable to occur.
- In the composite filaments according to the present invention, the conductive path may be exposed lengthwise intermittently on the surface of the filament. The portion to be exposed is the tip or a part of its vicinity of the conductive path. The length along the longitudinal axis of the filament of the exposed portion is not specifically defined. However, the proportion of the exposed length to the entire length of the filament is preferably not more than 90%, more preferably not more than 70%, most preferably not more than 50%. Too large the width or the length proportion of the exposed portion tends to cause metal abrasion.
- As explained above, the composite filaments according to the present invention have a novel crosssectional figure that is quite different from those of any conventional sheath-core or side by side type conductive composite filaments.
- The conjugate ratio, that is, the area ratio occupied by the conductive component in the cross-section of the composite filaments is preferably 3-40%, more preferably 4-20%, most preferably 5-15%. When the conjugate ratio is too small, the conductivity will decrease, lessening therefore the antistatic property. Alternatively, when it is too large, physical or mechanical properties of the filaments will be deteriorated and the metal abrasive property will be augmented.
- As the inorganic conductive particles to be used in the present invention, any kind of particles can be employed insofar as they have a specific resistance in powdery form of not more than about 104 Ω·cm. Not only those particles coated with a metal oxide or metal hydroxide having high whiteness but also metallic powders (e.g., silver, nickel, copper, iron, alloys thereof, etc.) and metallic compounds such as copper sulphide, copper iodide, zinc sulphide, cadmium sulphide and the like, can be employed.
- As metal oxide particles, mention may be made of particles of tin oxide, zinc oxide, copper oxide, cuprous oxide, indium oxide, zirconium oxide, tungsten oxide, etc. Most metal oxides are insulators or semi-conductors and do not show enough conductivity to satisfy the object of the present invention. However, the conductivity is increased, for example, by adding a small amount (not more than 50%, particularly not more than 25%) of a proper secondary component (impurity) to the metal oxide, whereby conductive metal oxide powders having sufficient conductivity to satisfy the object of the present invention can be obtained. As such a secondary component, i.e., a conductivity modifier, antimony oxide can be used for tin oxide, and also oxides of aluminum, gallium, indium, germanium, tin and the like for zinc oxide.
- Further, particles wherein a conductive film of the above-described metal oxides or other metallic compounds is formed on surfaces of non-conductive inorganic particles, such as titanium oxide, zinc oxide, magnesium oxide, tin oxide, iron oxide, silicon oxide, aluminum oxide and the like, also can be used. In the case where particularly high whiteness is required, it is preferred to use conductive particles which is obtained by mixing tin-oxide-coated titanium oxide particles with antimony oxide and firing the resulting mixture.
- The conductivity of the conductive metal oxide particles is preferred to be not more than about 10⁴ Ω·cm, particularly not more than about 10² Ω·cm, most preferably not more than about 10¹ Ω·cm in specific resistance in the powdery state. In fact, the particles having about 10² Ω·cm ∼ 10⁻² Ω·cm are obtained and can be suitably applied to the object of the present invention. The particles more excellent in conductivity are more preferable. The specific resistance (volume resistivity) is measured by charging 5 g of a sample into an insulative cylinder having a diameter of 1 cm and applying a pressure of 200 kg to the cylinder from the top by means of a piston and applying a direct current voltage (for example, 0.001-1,000 V, current of 1 mA or less).
- The conductive particles are preferred to be sufficiently small in the grain size. Particles having an average grain size of 1-2 m can be used but, in general, those having an average grain size of not more than 1 µm, particularly not more than 0.5 µm, most preferably not more than 0.3 µm, are suitably used.
- The term "grain size" used herein means the weight average diameter of single particles. A sample is observed by an electron microscope and is separated into single particles. Diameters (mean values of the long diameter and the short diameter) of about 1,000 particles are measured and classified by a unit of 0.01 µm to determine the grain size distribution and then the weight average grain size is determined from the following formulae (I) and (II).
Ni: Number of particles classified in No. i, and
Wi: Weight of particles classified in No. i.
Grain weightW= pD³
wherein
p : Density of particle, and
D : Diameter of particle. - The mixed ratio of the conductive particles in the conductive component depends upon the kind, conductivity, grain size, chain forming ability of particles, and the property, crystallinity, etc. of the polymer binder the particles are mixed with. However, it is generally within a range of about 10-85%, preferably about 20-80%, by weight. For example, the mixed ratio of titanium oxide particles coated with a conductive film is generally in the range of about 40-85%, more preferably 50-80%, most preferably 60-80%, by weight.
- The thermoplastic polymer to be mixed with the inorganic conductive particles, which forms the conductive component, is not particularly limited and can be selected arbitrarily from a host of thermoplastic polymers such as polyamides, polyesters, polyolefins, polyvinyls, polyethers and the like. These polymers are preferred to have fiber-formability from the standpoint of spinning operation. However, even though those polymers deficient in fiber-formability are used, composite filaments can be provided with sufficiently good spinnability by using a fiber-forming thermoplastic polymer as the non-conductive component to be conjugated therewith. As the thermoplastic polymers used for the conductive component, particularly preferred are those having a crystallinity of at least 60%, which are poor in compatibility with the non-conductive fiber-forming thermoplastic polymers. Such polymers include polyethylene, polypropylene, polyoxymethylene, polyethylene oxide and its derivatives (for example, ethylene oxide/ethylene terephthalate block copolymers), polyvinyl alcohol, polypivalolactone, polycaprolactone, etc. Among these polymers, polyethylene, polypropylene polyoxymethylene, and copolymers thereof, are particularly suitable.
- The conductive component is preferred to have a specific resistance (volume resistivity) of less than 10⁷ Ω·cm, more preferably not more than 10⁴ Ω·cm, and not more than 10² Ω·cm is particularly preferred.
- To the conductive component may be further added dispersants (for example, waxes, polyalkylene oxides, various surfactants, organic electrolytes, etc.), coloring agents, pigments, stabilizers (antioxidants, ultraviolet ray absorbents, etc.) flow improvers and other additives.
- As the fiber-forming thermoplastic polymers to form the non-conductive component in the composite filaments of the invention, any spinnable polymers can be used. Among the spinnable polymers, polyamides such as nylon-6, nylon-66, nylon-12, nylon-610 and the like, polyesters such as polyethylene terephthalate, polyethylene oxybenzoate, polybutylene terephthalate and the like, polyacrylonitrile and copolymers and modified polymers thereof, are particularly suitable. To the fiber-forming thermoplastic polymers may be added additives, such as delustrants, pigments, coloring agents, stabilizers, antistatic agents (such as polyalkylene oxides, various surfactants or the like). However, addition of inorganic particles in such a large amount as to possibly induce metal abrasion is not preferred. The non conductive component composed of a fiber-forming thermoplastic polymer as described above is preferred to have a specific resistance of at least 10⁷ Ω·cm.
- Meanwhile, in the conductive component of the composite filaments according to the present invention, the conductive core and conductive path usually have substantially the same composition. However, in a preferred embodiment, the thermoplastic polymer composition in the conductive path consists of a mixture of the polymer for the non-conductive sheath component with the polymer composition for the conductive core component. the mixing ratio of the both components is not specifically limited. However, a mixing ratio such as to bring the content in the mixture of the conductive inorganic particles into the range of 3-50%, particularly 5-40%, by weight, is preferred. If the content is too large, the composite filaments too much increase in metal abrasive property, while, if too small, the antistatic property becomes insufficient. The mixture is preferred to occupy at least the exposed portion on filament surfaces of the conductive path.
- The above-described polymer mixture can be produced according to any known processes. For example, use may be made of a process for mixing by means of a static mixer composed of relatively a few, preferably 1-3 mixing elements which is provided in a polymer flow path inside a spinneret assembly (FIG. 12), a mechanical mixer such as an impeller or rotor (FIG. 13), a hydrodynamic mixing utilizing collision of fluids caused by high pressure injection or a breaker such as glass beads or a filter layer provided in the flow path (FIG. 14), etc., and combinations thereof. In FIGS. 12-14, the numeral 101 denotes an entrance for a fiber-forming thermoplastic polymer; 102, an entrance for a conductive component polymer composition; 103, a static mixer; 104, a kneader; 105, a mixing zone; 106-108, meeting points; 109, a constriction device, and 110, a spinneret.
- The fiber-forming thermoplastic polymer and conductive component polymer composition to be mixed with each other are preferred to be mutually incompatible. Such a combination provides a mixture in a mutually phase-separated state. Alternatively, in the case of mutually compatible combinations, an unevenly mixed state, for example, a fine archipelagic or multi-layeredly dispersed state is preferred from the viewpoint of corona discharging.
- The reason why the excellent antistatic property and metal abrasion resistance that are the objects of the present invention are achieved by virtue of the specified figure of the conductive component comprising a thick conductive core and a conductive path of which only the tip reaches to the peripheral surface of the filament, is accounted as follows: the thick conductive core, for example, having a thickness of not less than 5 µm and a specific resistance of not more than about 10⁷ Ω·cm, extending continuously along the entire length of the filament, is considered to make movements in the longitudinal direction of the electric charge easy. This function, since the conductive core has a thickness larger than a certain degree, will not be deteriorated in processes such as drawing, false-twisting, rewinding, knitting, weaving and the like. Alternatively, since the conductive path conjoined with the thick conductive core reaches its tip up to or close to the surface of the filament and is exposed lengthwise continuously or intermittently, when the filaments are electrified, destaticization by corona discharge is considered to occur at a low potential.
- Thus, by incorporating the composite filaments of the present invention in a very small amount, fibrous articles provided with an excellent antistatic property can be produced without impairing aesthetic appearance, such as apparels, lingerie, foundations, hosiery, particularly working clothes for clean rooms, sheetings, carpets, upholsteries, interior cloths, or the like. The composite filaments of the invention may be mixed with other natural fibers or artificial fibers and used as continuous filament yarns, staple fibers, in a non-crimped, crimped, undrawn or drawn form.
- The present invention will be further explained by way of examples.
- In the examples, the antistatic property was evaluated according to the following method. An ordinary nylon-6 drawn yarn (210 deniers/54 filaments) was knit on a circular knitting machine, incorporating a conductive composite filament yarn in every eleventh course, to prepare a tubular knitted fabric mixed with 0.85% based on the weight of the fabric of the conductive composite filaments. The resulting fabric in which oils were removed by scouring was thoroughly washed with water, then dried at 80°C for 3 hours and further conditioned at 25°C in an atmosphere of 30% R.H. for 6 hours. Thereafter, the fabric was rubbed 15 times with a cotton cloth at the same temperature and humidity as the above, and the electrified charge after 10 seconds was measured.
- The metal abrasive property was measured by the time required for breaking a stainless steel wire having a diameter of 35 µm, when the filament yarn traveled on the stainless steel wire at a speed of 100 m/min. (The yarn tension before contacting was 4-5 g and the contact angle was 45°).
- The electric resistance was measured of a yarn consisting of 5 single filaments having a length of 10 cm. Both ends of the yarn were bonded to metal terminals with a conductive adhesive (Dodite D-550, manufactured by Fujikura Kasei K.K.), 10 V of direct current was applied between both the terminals, and the electric resistance was determined. The specific resistance of the conductive component was calculated from the above obtained value of the filament yarn.
- The following examples are given for the purpose of illustration of this invention and are not intended as limitations thereof.
- Conductive particles having an average grain size of 0.25 µm and a specific resistance of 6.3 Ω·cm was obtained by firing a mixture of titanium oxide particles coated with a tin oxide film and 0.75% by weight of said particles of antimony oxide. Seventyfive parts by weight of the above obtained particles and 25 parts by weight of polyethylene having a molecular weight of 80,000 were kneaded together to prepare a conductive polymer composition A₁. This conductive polymer composition A₁ and nylon-6 having a relative viscosity in 95% conc. H₂SO₄ of 2.3 were simultaneously spun from orifices having a diameter of 0.25 mm at a spinning temperature of 280°C into composite filament yarns having cross-sectional figures as shown in Table 1, with a conjugated ratio of 1/9 (areal raio in cross section). The as-spun yarns were taken up on a bobbin at a rate of 800 m/min., while cooling and oiling. Then the taken-up filament yarns were drawn at a draw ratio of 2.6 times on a hot roll at 80°C, further contacting with a plate heater at 170°C, to produce drawn yarns Y₁∼Y₅ of 20 deniers/3 filaments which were wound up on a pirn.
-
- Any of the yarns Y₁∼Y₅ had a specific resistance of not more than the order of 10³ Ω·cm and exhibited good conductivity. The yarns Y₁∼Y₃ and Y₅ had good antistatic properties but the yarn Y₄ that had not exposed the conductive polymer component on the filament surface was poor in antistatic property. Additionally, the yarns Y₁∼Y₄ had a little metal abrasive property but the yarn Y₅ exposing the conductive component largely in width on the surface of the filament had an extremely increased metal abrasive property. The yarn Y₅ could not be stably manufactured due to increased abrasion of thread guides.
- Next, the yarns Y₁∼Y₄ were respectively plied with a nylon-6 filament yarn of 2,600 deniers/140 filaments and the plied yarns were crimped by texturizing. Using the texturized yarn in every fourth course and only the nylon yarn in every three courses, a tufted carpet (looped, the mixed ratio of the conductive filaments: 0.17%) was produced. A charged voltage of a human body generated when a man putting on leather shoes walked on the resulting carpet in a room at 25°C with 20% R.H. was measured. The charged voltages of the carpets incorporated with the yarns Y₁∼Y₃ of the present invention were -2.0 kV, -2.3 kV and -1.8 kV, respectively. In contrast, that of the carpet incorporated with the yarn Y₄, a sheath-core type composite filament yarn, was -4.3 kV and an electric shock was received from a grounded doorknob. For the purpose of comparison, the charged voltage of human body of a carpet composed only of nylon was measured -9.2 kV and the electric shock received from the grounded doorknob was so violent that a considerable fear was felt.
- A polyethylene terephthalate polymer having a molecular weight of 15,000 blended with 0.65% based on the weight of the polymer of titanium oxide as a delustrant was used as a non-conductive polymer and the conductive polymer composition A₁ prepared in EXAMPLE 1 was used as a conductive polymer composition. These polymers were conjugated, in a spinneret, in side by side relation having a cross-sectional figure as shown in FIG. 3, and spun from orifices having a diameter of 0.3 mm at a spinning temperature of 285°C. After quenching and oiling, the as-spun filament yarn was wound up on a take-up roll at a rate of 1,000 m/min. Then the yarn was drawn 3.1 times its original length using a hot roll at 85°C, heat-set with a plate heater at 150°C and wound up on a pirn. Thus, conductive composite filament yarns Y6 Y9 were obtained. These filament yarns had properties shown in Table 2.
- Titanium oxide particles coated with tin oxide (SnO₂) and 1.5% based on the weight of the particles of antimony oxide were mixed together and fired to produce oonductive particles having an average grain size of 0.25 µm, a content of tin oxide of 15% by weight, a specific resistance of 7 Ω·cm and a whiteness, i.e., light reflection, of 83%. Seventy five parts by weight of the produced conductive particles and 25 parts by weight of a low density polyethylene having a molecular weight of about 50,000 and a melting point of 103°C were mixed and kneaded uniformly together with 0.5 parts by weight of magnesium stearate (a flow improver) to prepare a conductive polymer composition that was denoted as A₂. Nylon-6 having a molecular weight of about 16,000 and a melting point of 215°C admixed with 0.8% based on the weight of the nylon of titanium oxide to prepare a polymer B₁.
- The conductive polymer A₂ and the polymer B₁ were conjugate-spun with a conjugate ratio of 9/1 at a spinning temperature of 280°C from orifices having a diameter of 0.25 mm into composite filaments having cross-sectional figures as shown in Table 3. The as-spun filament yarns were wound up on a take-up roll at a rate of 800 m/min., while quenching and oiling. Then the yarns were drawn 2.6 times their original lengths with a hot roll at 80°C, further brought into contact with a plate heater at 170°C, and wound up on a pirn. Thus, drawn yarns Y₁₀ ∼Y₁₃ of 18 deniers/1 filament were obtained.
-
- Any Of the yarns Y₁₀∼Y₁₃, had a specific resistance of the order of 10³ Ω·Cm and exhibited good conductivity. The yarns Y₁₀∼Y₁₂ had a good antistatic property of not more than 2.0 kV, but the yarn Y₁₁ whose conductive polymer component was not exposed on the surface of the filaments had a poor antistatic property. Further, the yarns Y₁₀ and Y₁₁ had a decreased metal abrasive property, while the yarns Y₁₂ and Y₁₃ showed a considerably increased metal abrasive property. The yarns Y₁₂ and Y₁₃ abraded travellers so remarkably during draw-twisting operation that the stable manufacture of the yarns could not be performed. The yarn Y₁₀ was the only yarn that had a good antistatic property as well as a decreased metal abrasive property.
- A non-conductive polymer of polyethylene terephthalate having a molecular weight of 15,000, blended with 0.65 weight % of titanium oxide as a delustrant and the conductive polymer composition A₂ used in EXAMPLE 3, were conjugated, in a spinneret, in side by side relation such as cross sectional figures shown in Table 4, as covering the conjugated polymers with a thin sheath of the non-conductive polymer, and spun from orifices having a diameter of 0.3 mm at a spinning temperature of 282°C. After quenching and oiling, the as-spun filament yarn was wound up on a take-up roll at a rate of 1,000 m/min. Then the yarn was drawn 3.1 times its original length using a hot roll at 85°C, heat-set with a plate heater at 150°C and wound up on a pirn. Thus, composite filament yarns Y₁₄∼Y₁₇ were obtained. Those filament yarns had cross-sectional figures and properties shown in Table 4.
- On the peripheral surfaces of the yarns Y₁₄∼ Y₁₇, intermittent unevennesses caused by the conductive polymer were observed by SEM. All of these yarns exhibited substantially no metal abrasive property so that no troubles occurred in spinning, drawing, knitting and weaving processes. The yarns Y₁₄∼Y₁₆ had a good antistatic property. The yarn Y₁₇ that lacked the thick conductive core was high in specific resistance and poor in antistatic property.
- Titanium oxide particles coated with tin oxide and 0.75% based on the weight of the particles of antimony oxide were mixed together and fired to produce conductive particles having an average grain size of 0.25µm and a specific resistance of 6.3 Ω·cm. Seventyfive parts by weight of the produced conductive particles and 25 parts by weight of a polyethylene having a molecular weight of 80,000 were mixed and kneaded together to prepare a conductive polymer composition A₃.
- Using a spinning machine provided with a static mixer comprising a couple of mixing elements in a spinneret assembly such as shown in FIG. 12, 10 parts by volume of the above conductive polymer A₃ and 90 parts by volume of a nylon-6 (N₁) having a relative viscosity in 95% conc. H₂SO₄ of 2.3 were spun from orifices having a diameter of 0.25 mm at a spinning temperature of 280°C to form filaments with cross-sectional figures and mixing ratios as shown in Table 5. In the spinning, the polymers N₁ and A₃ were introduced from the
entrances constriction devices 109 were adjusted to control the mixing ratio. The as-spun filament yarns were wound up on a take-up roll at a rate of 800 m/min., while quenching and oiling. Then the yarns were drawn 2.6 times their original lengths with a hot roll at 80°C, further brought into contact with a plate heated at 170°C, and wound up on a pirn. Thus, drawn yarns Y₁₈ ∼Y₂₀ of deniers/3 filaments were obtained. -
- Any of the yarns Y₁₈∼Y₂₀ had a specific resistance of the order of 10² Ω·cm and exhibited good conductivity. The yarns Y₁₈ and Y₂₀ had a good antistatic property but the yarn Y₁₉ whose conductive polymer component was not exposed on the surface of the filaments had a poor antistatic property.
- Further, the yarns Y₁₈ and Y₁₉ had a decreased metal abrasive property, while the yarn Y₂₀ showed a considerably increased metal abrasive property and could not manufactured stably due to abrasion of thread guides.
- Next, the yarns Y₁₈ and Y₁₉ were respectively plied with a nylon-6 yarn of 2,600 deniers/140 filaments and the plied yarns were crimped by texturizing. Using the texturized yarn in every fourth course and only the nylon yarn in every three courses, a tufted carpet (looped, the mixed ratio of the conductive filaments: 0.17%) was produced. A charged voltage of a human body generated when a man putting on leather shoes walked on resulting carpet in a room at 25°C with 20% R.H. was measured. The charged voltage of the carpet incorporated with the yarn Y₁₈ of the present invention was -2.1 kV. In contrast, that of the carpet incorporated with the yarn Y₁₉, a sheath-core type composite filament yarn, was -4.3 kV and an electric shock was received from a grounded doorknob. For the purpose of comparison, the charged voltage of human body of a carpet composed only of nylon was measured -9.2 kV and the electric shock received from the grounded doorknob was so violent that a considerable fear was felt.
Claims (16)
(a) a non-conductive component composed of a fiber-forming thermoplastic polymer, forming a sheath extending along the entire length of the filament, and
(b) a conductive component consisting of a conductive core and a conductive path, being lapped in and extending lengthwise along said sheath, said conductive core being composed of a mixture of a thermoplastic polymer with inorganic conductive particles, said conductive path having a composition the same as or different from the conductive core, comprising a thermoplastic polymer and inorganic conductive particles,
which is characterized in that said conductive path extends laterally from a part of the periphery of said conductive core, transversely through the sheath, up to or close to the outer circumference of the sheath and that the conductive path is exposed at least partly lengthwise and not more than 1.5 µm in width on the outer peripheral surface of the sheath.
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62020860A JPS63190017A (en) | 1987-01-30 | 1987-01-30 | Antistatic conjugate fiber |
JP20860/87 | 1987-01-30 | ||
JP62069454A JPS63235525A (en) | 1987-03-23 | 1987-03-23 | Electrically conductive conjugated yarn |
JP69454/87 | 1987-03-23 | ||
JP62306233A JPH01148811A (en) | 1987-12-02 | 1987-12-02 | Production of electrically conductive conjugate fiber |
JP306233/87 | 1987-12-02 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0276756A2 true EP0276756A2 (en) | 1988-08-03 |
EP0276756A3 EP0276756A3 (en) | 1990-02-21 |
EP0276756B1 EP0276756B1 (en) | 1994-04-06 |
Family
ID=27283201
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP88100844A Expired - Lifetime EP0276756B1 (en) | 1987-01-30 | 1988-01-21 | Conductive composite filaments and fibrous articles containing the same |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0276756B1 (en) |
KR (1) | KR900008725B1 (en) |
CA (1) | CA1285358C (en) |
DE (1) | DE3888856T2 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0343496A2 (en) * | 1988-05-27 | 1989-11-29 | Kuraray Co., Ltd. | Conductive composite filament and process for producing the same |
DE9108057U1 (en) * | 1991-07-01 | 1991-08-22 | August Mink KG, 7320 Göppingen | Technical brush with roller or strip-shaped brush body and, depending on the respective application, a wide variety of bristles |
US5126201A (en) * | 1988-12-28 | 1992-06-30 | Kao Corporation | Absorbent article |
DE4110279A1 (en) * | 1991-03-28 | 1992-10-01 | Alfo Ag | LIGHT GUIDE |
WO1996028611A1 (en) * | 1995-03-13 | 1996-09-19 | Arjo Wiggins S.A. | Security paper with conductive fibres detectable by microwave radiation and method for making same |
WO1996037656A1 (en) * | 1995-05-24 | 1996-11-28 | Arjo Wiggins S.A. | Security paper |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2001901A (en) * | 1977-08-08 | 1979-02-14 | Kanebo Ltd | Conductive composite filaments |
GB2077182A (en) * | 1980-06-06 | 1981-12-16 | Kanebo Ltd | Conductive composite filaments |
-
1988
- 1988-01-14 CA CA000556540A patent/CA1285358C/en not_active Expired - Lifetime
- 1988-01-21 EP EP88100844A patent/EP0276756B1/en not_active Expired - Lifetime
- 1988-01-21 DE DE3888856T patent/DE3888856T2/en not_active Expired - Lifetime
- 1988-01-30 KR KR1019880000844A patent/KR900008725B1/en active Pre-grant Review Request
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2001901A (en) * | 1977-08-08 | 1979-02-14 | Kanebo Ltd | Conductive composite filaments |
GB2077182A (en) * | 1980-06-06 | 1981-12-16 | Kanebo Ltd | Conductive composite filaments |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0343496A2 (en) * | 1988-05-27 | 1989-11-29 | Kuraray Co., Ltd. | Conductive composite filament and process for producing the same |
EP0343496A3 (en) * | 1988-05-27 | 1990-10-31 | Kuraray Co., Ltd. | Conductive composite filament and process for producing the same |
US5126201A (en) * | 1988-12-28 | 1992-06-30 | Kao Corporation | Absorbent article |
DE4110279A1 (en) * | 1991-03-28 | 1992-10-01 | Alfo Ag | LIGHT GUIDE |
DE9108057U1 (en) * | 1991-07-01 | 1991-08-22 | August Mink KG, 7320 Göppingen | Technical brush with roller or strip-shaped brush body and, depending on the respective application, a wide variety of bristles |
WO1996028611A1 (en) * | 1995-03-13 | 1996-09-19 | Arjo Wiggins S.A. | Security paper with conductive fibres detectable by microwave radiation and method for making same |
WO1996037656A1 (en) * | 1995-05-24 | 1996-11-28 | Arjo Wiggins S.A. | Security paper |
Also Published As
Publication number | Publication date |
---|---|
EP0276756B1 (en) | 1994-04-06 |
KR880009536A (en) | 1988-09-15 |
KR900008725B1 (en) | 1990-11-27 |
EP0276756A3 (en) | 1990-02-21 |
DE3888856D1 (en) | 1994-05-11 |
DE3888856T2 (en) | 1994-08-18 |
CA1285358C (en) | 1991-07-02 |
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