CA1256052A - Tows and yarns of high strength electroplated carbon fibers - Google Patents
Tows and yarns of high strength electroplated carbon fibersInfo
- Publication number
- CA1256052A CA1256052A CA000423551A CA423551A CA1256052A CA 1256052 A CA1256052 A CA 1256052A CA 000423551 A CA000423551 A CA 000423551A CA 423551 A CA423551 A CA 423551A CA 1256052 A CA1256052 A CA 1256052A
- Authority
- CA
- Canada
- Prior art keywords
- metal
- core
- layer
- fibers
- yarn
- 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
Links
- 229920000049 Carbon (fiber) Polymers 0.000 title description 13
- 239000004917 carbon fiber Substances 0.000 title description 13
- 239000000835 fiber Substances 0.000 claims abstract description 130
- 229910052751 metal Inorganic materials 0.000 claims abstract description 93
- 239000002184 metal Substances 0.000 claims abstract description 93
- 239000002131 composite material Substances 0.000 claims abstract description 68
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 67
- 238000000034 method Methods 0.000 claims abstract description 54
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 34
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 33
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 18
- 230000001464 adherent effect Effects 0.000 claims abstract description 11
- 238000004519 manufacturing process Methods 0.000 claims abstract description 8
- 238000004070 electrodeposition Methods 0.000 claims abstract description 4
- 239000000463 material Substances 0.000 claims description 20
- 238000000576 coating method Methods 0.000 claims description 17
- 239000011133 lead Substances 0.000 claims description 16
- 239000011248 coating agent Substances 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 13
- 239000011159 matrix material Substances 0.000 claims description 11
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 10
- 229910052802 copper Inorganic materials 0.000 claims description 10
- 239000010949 copper Substances 0.000 claims description 10
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 7
- 230000006835 compression Effects 0.000 claims description 7
- 238000007906 compression Methods 0.000 claims description 7
- 239000004744 fabric Substances 0.000 claims description 7
- 229910052709 silver Inorganic materials 0.000 claims description 7
- 239000004332 silver Substances 0.000 claims description 7
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 6
- 229920000914 Metallic fiber Polymers 0.000 claims description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 6
- 230000015556 catabolic process Effects 0.000 claims description 6
- 238000006731 degradation reaction Methods 0.000 claims description 6
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052737 gold Inorganic materials 0.000 claims description 6
- 239000010931 gold Substances 0.000 claims description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 6
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 6
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 6
- 229910052725 zinc Inorganic materials 0.000 claims description 6
- 239000011701 zinc Substances 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 5
- 230000003014 reinforcing effect Effects 0.000 claims description 5
- 238000000926 separation method Methods 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 4
- 238000000151 deposition Methods 0.000 claims description 4
- 238000007654 immersion Methods 0.000 claims description 4
- 229910052580 B4C Inorganic materials 0.000 claims description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 3
- 229910001338 liquidmetal Inorganic materials 0.000 claims description 3
- 229910052697 platinum Inorganic materials 0.000 claims description 3
- 229910052718 tin Inorganic materials 0.000 claims description 3
- 239000011135 tin Substances 0.000 claims description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052721 tungsten Inorganic materials 0.000 claims description 3
- 239000010937 tungsten Substances 0.000 claims description 3
- 229910052785 arsenic Inorganic materials 0.000 claims description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 2
- 229910052793 cadmium Inorganic materials 0.000 claims description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 229910052738 indium Inorganic materials 0.000 claims description 2
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 2
- 229910052741 iridium Inorganic materials 0.000 claims description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- 238000004064 recycling Methods 0.000 claims description 2
- 229910052714 tellurium Inorganic materials 0.000 claims description 2
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 claims description 2
- 238000009940 knitting Methods 0.000 claims 2
- 238000009941 weaving Methods 0.000 claims 2
- 229940000425 combination drug Drugs 0.000 claims 1
- 239000010410 layer Substances 0.000 description 29
- 229910002804 graphite Inorganic materials 0.000 description 16
- 239000010439 graphite Substances 0.000 description 16
- 150000002739 metals Chemical class 0.000 description 13
- 239000004033 plastic Substances 0.000 description 9
- 229920003023 plastic Polymers 0.000 description 9
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 238000007747 plating Methods 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- -1 R.V. Sara Chemical class 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 239000003792 electrolyte Substances 0.000 description 4
- 238000009713 electroplating Methods 0.000 description 4
- 230000002787 reinforcement Effects 0.000 description 4
- 229910001369 Brass Inorganic materials 0.000 description 3
- 241001131688 Coracias garrulus Species 0.000 description 3
- 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 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052796 boron Inorganic materials 0.000 description 3
- 239000010951 brass Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229910021645 metal ion Inorganic materials 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- 230000002441 reversible effect Effects 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000002344 surface layer Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- JHWIEAWILPSRMU-UHFFFAOYSA-N 2-methyl-3-pyrimidin-4-ylpropanoic acid Chemical compound OC(=O)C(C)CC1=CC=NC=N1 JHWIEAWILPSRMU-UHFFFAOYSA-N 0.000 description 2
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000008151 electrolyte solution Substances 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 230000006911 nucleation Effects 0.000 description 2
- 238000010899 nucleation Methods 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 2
- 238000005494 tarnishing Methods 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 238000001771 vacuum deposition Methods 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- 229920002430 Fibre-reinforced plastic Polymers 0.000 description 1
- 239000001828 Gelatine Substances 0.000 description 1
- 229910004039 HBF4 Inorganic materials 0.000 description 1
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 101100216234 Schizosaccharomyces pombe (strain 972 / ATCC 24843) cut20 gene Proteins 0.000 description 1
- 229920001229 Starlite Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 235000011124 aluminium ammonium sulphate Nutrition 0.000 description 1
- LCQXXBOSCBRNNT-UHFFFAOYSA-K ammonium aluminium sulfate Chemical compound [NH4+].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O LCQXXBOSCBRNNT-UHFFFAOYSA-K 0.000 description 1
- 229910003481 amorphous carbon Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 230000002844 continuous effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 239000011151 fibre-reinforced plastic Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 238000005087 graphitization Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 1
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 150000002843 nonmetals Chemical class 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- LFAGQMCIGQNPJG-UHFFFAOYSA-N silver cyanide Chemical compound [Ag+].N#[C-] LFAGQMCIGQNPJG-UHFFFAOYSA-N 0.000 description 1
- 229940098221 silver cyanide Drugs 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/22—Yarns or threads characterised by constructional features, e.g. blending, filament/fibre
- D02G3/36—Cored or coated yarns or threads
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F41—WEAPONS
- F41J—TARGETS; TARGET RANGES; BULLET CATCHERS
- F41J2/00—Reflecting targets, e.g. radar-reflector targets; Active targets transmitting electromagnetic or acoustic waves
-
- 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
- D01F11/00—Chemical after-treatment of artificial filaments or the like during manufacture
- D01F11/10—Chemical after-treatment of artificial filaments or the like during manufacture of carbon
- D01F11/12—Chemical after-treatment of artificial filaments or the like during manufacture of carbon with inorganic substances ; Intercalation
- D01F11/127—Metals
-
- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/44—Yarns or threads characterised by the purpose for which they are designed
- D02G3/441—Yarns or threads with antistatic, conductive or radiation-shielding properties
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Electromagnetism (AREA)
- Remote Sensing (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Radar, Positioning & Navigation (AREA)
- Physics & Mathematics (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Ropes Or Cables (AREA)
- Manufacture Of Alloys Or Alloy Compounds (AREA)
- Woven Fabrics (AREA)
- Knitting Of Fabric (AREA)
- Nonwoven Fabrics (AREA)
- Laminated Bodies (AREA)
Abstract
TITLE: YARNS AND TOWS COMPRISING HIGH STRENGTH
METAL COATED FIBERS, PROCESS FOR THEIR
PRODUCTION, AND ARTICLES MADE THEREFROM
ABSTRACT OF THE DISCLOSURE
Yarns or tows of high strength composite fibers the majority of which comprise a core of carbon or the like and a thin, uniform firmly adherent electrically conductive layer or an electro-depositable metal, such as nickel or the like, the bond strength of the metal to the core being greater than 10 percent of the intermetallic bond strength of the metal layer. The composites can be produced by electrodeposition from a bath onto the core but the procedure must use external voltages high enough both (i) to dissociate the metal at the core and (ii) to nucleate the metal through the boundary layer into direct contact with the core.
METAL COATED FIBERS, PROCESS FOR THEIR
PRODUCTION, AND ARTICLES MADE THEREFROM
ABSTRACT OF THE DISCLOSURE
Yarns or tows of high strength composite fibers the majority of which comprise a core of carbon or the like and a thin, uniform firmly adherent electrically conductive layer or an electro-depositable metal, such as nickel or the like, the bond strength of the metal to the core being greater than 10 percent of the intermetallic bond strength of the metal layer. The composites can be produced by electrodeposition from a bath onto the core but the procedure must use external voltages high enough both (i) to dissociate the metal at the core and (ii) to nucleate the metal through the boundary layer into direct contact with the core.
Description
1;2~6~5~
YARNS AND TOWS COMPRISING HIGH
STRENGTH METAL COATED FIBERS, PROCESS FOR THEIR PRODUCTION, AND ARTICLES MADE THEREFROM
The present invention relates to continuous yarns and tows comprising high strength bundles of composite fibers compris-ing conductive semi-metallic cores coated with thin adherent layers of metals, to methods for their production, and to articles made from such yarns.
, ~2S6(~52 BACKGROUND OF THE INVENTION
Bundles of high strength fibers of non-metals and semi-metals, such as carbon, boron, silicon carbide, and the like, in the form of filaments, mats, cloths and chopped strands are known to be ~seful in reinforcing metals an~ organic polymeric materials. Articles com-prising metals or plastics reinforced with such fibers find wide-spread use in replacing heavier components made of lower strength conventional materials such as aluminum, steel, titanium, vinyl polymers, nylons, polyesters, etc., in aircraft, automobiles, office equipment, sporting goods, and in many other fields.
A common problem in the use of such fibers, and also glass, asbestos, and others, is a seeming lack of ability to translate the properties of the high strength fibers to the material to which ultimate and intimate con-tact is to be made.
The problem is manifested in a variety of ways:
for example, if a length of high strength carbon fiber yarn is enclosed lengthwise in the center of a rod formed from solidified molten lead, and the rod is pulled until broken, 25 the breaking strength will be less than expected from the rule of mixtures, and greater than that of a rod formed from lead alone, due to the mechanical entrapment of the fibers. The lack of reinforcement strength is entirely due to poor translation of strength between the carbon fibers and the 30 lead. The same thing happens if an incompatible high strength fiber is mixed with a plastic material. If some types of carbon fibers, boron fibers, silicon carbide fibers, and the like in the forms of strands, chopped strands, non-woven mats, felts, papers, etc. or woven fabrics are mixed 35 w;th or~anic Dolymeri~ substances. such as phenolics B
lZS6~S2 styrenics, epoxy resins, polycarbonates, and the like, or mixed into molten metals, such as lead, aluminum, titanium, etc., they merely fill them without providing any reinforce-ment, and in many cases even cause physical properties to deteriorate.
All of these problems are generally recognized now, after years of research, to result from the need to insure adequate bonding between the high strength fiber and the so-called matrix materlal, the metal or plastic sought to be reinforced. It is also known that bonding can be improved with careful attention to the surface layer on each~
macro-micro filament or fibril in the material selected for use. Glass filaments, for example, are flame cleaned and 15 then sized with a plastic-compatible organosilane to produce reinforcements uniquely suitable for plastics.
Such techni~ues do not work well with other fibrous materials and, for obvious reasons, are not suitable 20 for carbon fibers, which would not have surface texture, and which have different boundary layers.
High stength carbon fibers are made by heating polymeric fiber, e.g., acrylonitrile polymers or copolymers, 25 in two stages, one to remove volatiles and carbonize and another to convert amorphous carbon into crystalline carbon.
During such procedure, it is known that the carbon changes from amorphous to single crystal then orients into fibrils.
If the fibers are stretched during the graphitization, then 30 high strength fibers are formed. This is critical to the formation of the boundary layer, because as the crystals grow, there are formed high surface energies, as exemplified by incomplete bonds, edge-to-edge stresses, differences in morphology, and the like. It is also known that the new 35 carbon fibrils in this form can scavenqe nascent oxygen ~,,1~
,,,~' lZ56~S2 from the air7 and even organic materials, to produce non-carbon surface layers which are firmly and chemically bonded thereto, although some can be removed by solvent treating, and there are some gaps or open spaces in the boundary layers.
Not unlike the contaminants on uncleaned, unsized glass fila-ments, these boundary layers on carbon fibers are mainly responsib~e for failure to achieve reinforcement with plastics and metals.
Numerous unsuccessful attempts have been reported to provide such filaments, especially carbon filaments, in a form uniquely suitable for reinforcing metals and plastics.
Most have involved depositing layers of metals, especially nickel and copper as thin surface layers on the filaments.
Such a composite filament was then to be used in a plastic or metal matrix. The metals in the prior art procedures have been vacuum deposited, electrolessly deposited, and electro-lytically deposited, but the resulting composites were not suitable.
Vacuum deposition, e.g., of nickel, U.S. 4,132,828, made what appears to be a continuous coating, but really isn't because the vacuum deposited metal first touches the fibrils through spaces in the boundary layer, then grows outwardly like a mushroom, then joins away from the surface, as observed under a scannins electron microscope as nodular nucleation. If the fiber is twisted, such a coating will fall off. The low density non-crystalline deposit limits use.
Electroless nickel baths have also been employed to plate such fibers but again there is the same problem, the initial nickel or other electroless metal seeds only small spots through holes in the boundary layer, then new 35 metal grows up like a mushroom and joins into what looks --- 12~(3S2 like a contlnuous coating, but it too will fall off when the fiber is twisted. The intermetallic compound is very locally nucleated and this, too, limits use. In the case of both vacuum deposition and electroless deposition, the strength of the metal-to-core bond is always substantially less than one-tenth that of the tensile strength of the : metal deposit itself.
Finally, electroplating with nickel and other metals is also featured in reported attempts to provide carbon fibers with a metal layer to make them compatible with metals and plastics, e.g., R.V. Sara, U.S. 3,622,283.
Short lengths of carbon fibers were clamped in a battery clip, immersed in an electrolyte, and electroplated with lS nickel. When the plated fibers were put into a tin metal matrix, the fibers did not translate their strength to the matrix to the extent expected from the rule or mixtures.
When fibers produced by such a process are sharply bent, on the compression side of the bend there appear a number of 20 transverse cracks and on the tension side of the bend the metal breaks and flakes off. If the metal coating is mechanically stripped, and the reverse side is examined under a high-power microscope, there is either no replica or at best only an incomplete replica of the fibril, the 25 replica defined to the 40 angstrom resolution of the scan-ning electron microscope. The latter two observations are strongly suggestive that failure to reinforce the aluminum matrix was due to poor bonding between the carbon and the nickel plating. In these cases, the metal to core bond 30 strength is no greater than one-half of the tensile strength on at most 10% of the fibers, and substantially less than one-tenth on the remaining 90~.
It has now been discovered that if electroplating 35 is selected, and if a very high order of external voltage is ~l~S6~5~
applied, much higher than was thought to be achievable in the prior art, uniform, continuous adherent, thin metal coatings can be provided to reinforcing fibrils, especially carbon fibrils. The voltage must be high enough to provide energy sufficient to push the metal ions through the boundary layer to provide uniform nucleation with the fibrils directly.
Composites of yarns or tows comprising the thin metal coat-ings on fibers, woven cloth, yarns, and the like, according to this invention can be knotted and folded without the metal flaking off. The composites are distinguishable from any of the prior art because they can be sharply bent without the fibrils slipping through a tube of the metal, as observed with electroless metal or vacuum deposited composites and sharply bending them, especially with nickel, produces - 15 neither transverse cracking ("alligatoring") on the compres-sion side of the bend nor breaking and flaking when the elastic limit of the metal is exceeded on the tension side - of the bend. In other words, the composites of the present invention are distinguishable from those of the prior art 20 because (i) they are continuous, (ii) the majority of the composite fibers are uniformly metal coated; and (iii) the bond strength (metal-to-core) on the majority of fibers is at least about 10 percent of the tensile strength of the metal deposit, preferably not substantially less than about 25 per-25 cent, especially preferably not substantially less than about50 percent. In the most preferred embodiments, the metal-to-core bond strength will be not substantially less than about 90 percent of the tensile strength of the metal deposit.
Highest properties will be achieved with yarns or tows of 30 composite fibers in which the metal-to-core bond strength approaches about 99 percent of the tensile strength of the metal, and special mention is made of these.
Articles made by adding the yarns or tows of the 35 present invention to a matrix forming material also dis-110-014 12~6~52 tinguish from the prior art because they are strongly reinforced. In addition, th~ articles possess other advantages, for example, they dissipate electrical charges and if certain innocuous metals are used in the coatings, e.g., gold and platinum, they will not be rejected when im-planted into the body.
' 10 ~ZS~S~
BRIEF DESCRIPTION OF THE DRAWINGS
The invention may be more readily understood by reference to the accompanying drawings in which:
Fig. 1 is a transverse cross sectional view of a metal coated fiber of this invention.
Fig. la is a longitudinal cross sectional view of a metal fiber according to this invention.
Fig. 2 and 2a are transverse cross sectional views of, respectively, a multinodal core and a "cracked"
core fiber coated with metal according to this invention.
Fig. 3 shows a longitudinal cross section of sharply bent metal coated fiber according to this invention;
and Fig. 3a shows a longitudinal cross section of a sharply bent metal coated composite prepared according to the prior art;
Fig. 4 is a partial sectional view of a metal coated composite fiber-reinforced polymer obtained by using this invention; and Fig. 5 is a view showing an apparatus for carry-ing out the process of the present invention.
All the drawings represent models of the articles described.
~25~52 SUMMARY OF THE INVENTION
In this disclosure the following terms are used with the following ~eanings:
fiber - the untreated material employed in the process of the invention to produce composite fiber composite fiber - metal-coated fiber of the invention core - central portion of the composite fiber (derived from the fiber) metal layer - the outer metal portion of the composite fiber.
(or layer) According to the present invention, there is provided a continuous yarn or tow comprising high strength composite fibers, the majority of which have an electrically conductive semi-metallic core and at least one thin, uniform and firmly adherent, electrically conductive layer of at least one metal on said core. Preferably the bond strength of said layer to said core being not substantially less than about 10 percent of the tensile strength of the metal. The bond strength of the layer to the core preferably is at least sufficient to provide that when the composite fiber is bent sharply enough to break the layer on the tension side of the bend because its elastic limit is exceeded, the layer on the compression side of the bend will remain bonded to the core and will not crack circumferentially.
Preferably the continuous yarn or tow can be knotted without substantial separation and loss of the metal layer.
In preferred features the core comprises carbon, boron or silicon carbide, especially carbon fibrils.
The most preferred yarns of composite fibers will be 1~56Q5Z
those in which, when the coating is removed by mechanical means and examined, there will be a replica of the fiber or fibril surface on the innermost surface of the removed coating, as examined under a scanning electron microscope of a definition of 40 angstroms or better.
Among the features of the invention are knottable tows or yarns of the new composite fibers, fabrics woven from such yarns (alone or with yarns which are of different material), non-woven sheets, mats and papers laid up from such fibers, chopped strands of such fibers and articles comprising such fibers uniformly dispersed in a matrix comprising a metal or an organic polymeric material. In preferred embodiments, coating metals will be nickel, silver, zinc, copper, lead, arsenic, cadmium, tin, cobalt, gold, indium, iridium, iron, palladium, platinum, tellurium, tungsten or a mixture of any of the fore-going, without limitation, preferably in crystalline form.
The invention further provides a continuous yarn or tow comprising high strength composite fibers, the majority of which have an electrically conductive semi-metallic substantially undegraded core and at least one thin, uniform and firmly adherent, electrically conductive layer of at least one metal on said core. Preferably the metal is a high voltage electrodeposited metal. Particularly preferred is a continuous yarn or tow of this type wherein the layer has been electrodeposited in an electro-deposition bath at an applied external voltage in excess of 10 volts while maintaining the yarn or tow cool enough outside the bath to prevent degradation of the continuous fibers.
12S~52 ~ 61109-7188 In another principal aspect of the present invention there is provided a process for the production of a continuous yarn or tow of high strength composite fibers having a fiber core and at least one thin, uniform, and firmly adherent electrically conductive layer of at least on~ metal adhered thereto; said process comprising:
(a) providing a continuous length of a plurality of electrically conductive semi-metallic fibers;
(b) continuously immersing at least a portion of the 10 length of said fibers in a bath capable of electrolytically depositing at least one metal thereon, (c) applying an external voltage in excess of 10 volts, (d) maintaining said voltage and resulting current, for a time sufficient to produce composite fibers comprising a thin, uniform, firmly adherent, electrically conductive layer of electrolytically deposited metal on said fibers each said fiber forming a core of each said composite fiber, (e) cooling the composite fibers as they leave the bath, for a time sufficient to prevent degradation of the said composite fibers, and (f) forming a yarn or tow from said composite fibers.
Preferably the applied external voltage is between 10 and 50 volts particularly between 12 and 36 volts and especially in excess of 13 volts.
In preferred features, the process will use core fibers of carbon, boron or silicon carbide, especially carbon fibrils.
Preferably the composite fibers are maintained cool enough by means outside the bath so that degradation is substant--lla- 61109-7188 ially avoided by recycling the liquid contents of the bath into contact with the fiber prior to immersion therein and with the composite fibers immediately subsequent to immersion therein.
A further aspect of the invention provides a process for preparing a reinforced composite which comprises intimately - contacting a liquid metal or a liquid organic material with at least a reinforcing amount of a fabric, a non-woven sheet or a chopped yarn, each as described above. Such a reinforced compos-ite thereby produced preferably forms a reinforced electrostati-cally shielded composite.
''0-014 _12 _ DETAILED DESCRIPTION OF THE INVENTION
Referring to Figs. 1 and la continuous yarns and tows for use in the core 2 according to the present invention are available from a number of sources commercially. For example, suitable carbon fiber yarns are available from Hercules Company, Hitco, Great Lakes Carbon Company, AVCO
Company and similar sources in the United States, and overseas. All are made, in general, by procedures des-10 cribed in U.S. 3,677,705. The fibers can be long and con-tinuous or they can be short, e.g., 1 to 15 cm. in length.
As mentioned above, all such carbon fibers will contain a thin, imperfect boundary layer (not shown) of chemically bonded oxygen and chemically or mechanically bonded other materials, such as organics.
Metal layer 4 will be of any electrodepositable metal, and it will be electrically continuous. Two layers, or even more, of metal can be applied and metal can be the same or different, as will be shown in the working examples.
In any case, the innermost layer will be so firmly bonded to core 2 that sharp bending will neck the metal down as shown in Fig. 3, snapping the fiber core and breaking the metal on the tension side of the bend when its elastic limit is exceeded. This is accomplished without causing the metal to flake off when broken (Fig. 3a), which is a problem in fibers metal coated according to the prior art.
As a further distinction from the prior art, the metal layer of the present invention fills interstices and "cracks" in fibers, uniformly and completely, as illustrated in Figs. 2 and 2a.
The high strength metal coated fibers of this invention can be assembled by conventional means into com-posites represented in Fig. 5 in which matrix 6 is a 1~ 014 1~'~6~SZ
_ 13 -o plastic, e.g., epoxy resin, or a metal, e.g., lead, the matrix being reinforced by virtue of the presence of high strength fibrous cores 2.
Formation of the metal coating layer by the electrodeposition process of this invention can be carried out in a number of ways. For example, a plurality of core fibers can be immersed in an electrolytic bath and through suitable electrical connections the required high external voltage can be applied. In one manner of proceeding, a high order of voltage is applied for a short period of time.
A pulse generator, for example, will send a surge of voltage through the electrolyte, sufficient to push or force the metal ion through the boundary layer into contact with the carbon or other fiber comprising the cathode. The short time elapsing in the pulse will prevent heat from building up in the fiber and burning it up or out. Because the fibers are so small, e.g., 5 to 10 microns in diameter, and because the innermost fibers are usually surrounded by hundreds or even thousands of others, even though only 0.5 to 2.6 volts are needed to dissociate the electrolytic metal ion, e.g., nickel, gold, silver, copper, depending on the salt used, massive amounts of external voltage are needed, of the order of 5 times the dissociation values, to uniformly nucleate the ions through the bundle of fibers into the innermost fibril and then through the boundary layer. Mini-mum external voltages of e.g., lO to 50, or even more, volts - are necessary.
Although pulsing as described above is suitable for small scale operations, for example, to metallize pieces of woven fabrics, and small lengths of carbon fiber yarns or tows, it is preferred to carry out the procedure in a continuous fashion on a moving tow of fibers. To over-come the problem of fiber burnout because of the high voltages, lZ5~(~52 to keep them cool enough outside the bath, one can separate the fibers and pour water on them,for example, but it is preferred to operate in an apparatus shown schematically in Figure 5. Electro-lytic bath solution 8 is maintained in tank 10. Also included are anode baskets 12 and idler rolls 14 near the bottom of tank 10.
Two electrical contact rollers 16 are located above the tank. Tow 24 is pulled by means not shown off feed roll 26, over first con-tact rol-ler 16 down into the bath under idler rolls 14, up through the bath, over second contact roller 16 and into take up roller 28. By way of illustration, the immersed tow length is about 6 feet. Optional, but very much preferred, is a simple loop compris-ing pump 18, conduit 20, and feed head 22. This permits recircu-lating the plating solution at a large flow rate, e.g., 2-3 gallons/
min. and pumping it onto contact rolls 16. Discharged just above the rolls, the sections of tow 24 leaving the solution are totally bathed with recirculated electrolyte, thus cooling them.
At the high current carried by the tow fibers, the I2R heat gener-ated in some cases might destroy them before they reach or after they leave the bath surface without such cooling. The flow of the electrolyte overcomes anisotropy. Of course, more than one plating bath can be used in series, and the fibers can be rinsed free of electrolyte solution, treated with other conventional materials and dried, chopped, woven into fabric, all in accordance with conventional procedures.
~' ., ,, ~ .
~2S6(~S2 - 15 _ DESCRIPTION OF THE PREFERRED EMBODIMENTS
The following Examples illustrates the present invention, but are not intended to limit it.
In a continuous electroplating system, a bath is provided having the following composition:
Ingredient Amount -nickel sulfate (NiSO4.6~2O) 40 ounces/gallon nickel chloride (NiC12.6H2O) 12 20 ounces/gallon boric acid (H3BO3) 5-8 ounces/gallon wetting agent (WA-129*, State 2% by volume Chemical) brightener (Starlite 915, State 2% by volume Chemical) The bath is heated to 140-160F and has a pH of 3.8-4.2.
The anode baskets are kept filled with electrolytic nickel pellets and 4 tows (fiber bundles) of 12,000 strands each of 7 micron carbon fibers are continuously drawn through the bath while an external voltage of 30 volts is applied at a current adjusted to give 10 ampere-minutes per 1000 strands total. At the same time,electrolytic solution is recycled through a loop into contact with the entering and leaving parts of the tow. The tow is next passed continuously through an identical bath, at a tow speed of 5.0 ft./min.
with 180 amps. current in each bath. The final product is a tow of high strength composite fibers according to this invention comprising a 7 micron fiber core and`about 50% by weight of the composite of crystalline electrodeposited nickel * I'rademark 110-014 1~56~S~
adhered firmly to the core.
If a length of the fi~er is sharply bent, then examined, there is no circumferential cracking on the metal coating in the tension side of the bend. The tow can be twisted and knotted without causing the coating to flake or come off as a powder. If a section of the coating is mechanically stripped from the fibrils, there will be a perfect reverse image (replica) on the reverse side. -If the procedure of Example 1 is repeated,substituting two baths of the following compositions, in series, and using silver in the anode baskets, silver coated graphite fibers according to this invention will be obtained.
Ingredient First BathSecond Bath Silver Cyanide 0.1-0.3 oz./gal.7-11 oz./gal.
Potassium Cyanide 12 - 20 oz./gal.12 oz./gal.
Potassium Hydroxide - - - 1- 2 oz./gal.
The first bath is to be operated at room tempera-ture and 12-36 volts; the second at room temperature and 6-18 volts.
The procedure of Example 2 can be modified, by substituting nickel plated graphite fibers as prepared in Example 1 for the feed, and the voltage in the first bath is reduced to about 18 volts. There are obtained high strength composite fibers according to this invention in 110-014 ~256~S2 which a silver ccating surrounds a nickel coating on a graphite fiber core.
The procedure of Example 1 can be modified by substituting for the nickel bath a bath of the following composition, using zinc in the anode baskets, and zinc coated graphite fibers according to this invention will be obtained:
Ingredient Amount Zinc sulfate 8 oz./gal.
Ammonium alum 3-4 oz./gal.
Potassium hydroxide 16 oz./gal.
Potassium cyanide 3 oz./gal.
The bath is run at 100F and 18 volts are externally applied.
The procedure of Example 1 can be modified by substituting for the nickel bath a bath of the following composition, using copper in the anode baskets, and copper coated graphite fibers according to this invention will be obtained:
Ingredient Amount Copper cyanide 3.5 oz./gal.
Sodium cyanide ~4.6 oz./gal.
Sodium carbonate 4 oz./gal.
Sodium hydroxide 0.5 oz./aal.
Rochelle salt 6 oz./gal.
.
The bath is run at 140F and 18 volts are externally applied. The copper plated fibers should be washed with sodium dichromate solution immediately after plating to prevent tarnishing. If the procedure of Example 3 is repeated, substituting the copper bath of this example for the silver bath, there will be obtained high strength composite fibers according to this invention in which a copper coating surrounds a nickel coating on a graphite fiber core.
The procedure of Example 1 can be modified by substituting for the nickel bath two baths of the following composition, using standard 80% cut20~ zinc anodes, and brass coated graphite fibers according to this invention will be obtained:
Ingredient Amount Copper cyanide4 oz./gal.
Zinc cyanide1.25 oz./gal.
Sodium cyanide7.5 oz./gal.
Sodium carbonate4 oz./gal.
Both baths are run at 110-120F. Since one-third of the brass is plated in the first bath, at 24 volts, and two-thirds in the second at 15 volts, the current is pro-portioned accordingly. Following two water rinses, the 30 brass plated fibers are washed with a solution of sodium dichromate, to prevent tarnishing, and then rinsed twice again with water.
lZ56~S2 The procedure of Example 1 can be modified by substituting for the nickel bath a bath of the following composition, using solid lead bars in the anode baskets, and lead coated graphite fibers according to this inven-tion wilI be obtained:
Inqredient Amount Lead fluoborate, Pb(BF4)2 14 oz. Pbtga Fluoboric acid, HBF4 13 oz./gal.
Optionally, about 2 g./l. each of ~-naphthol and of gelatine are added. The pH is less than 1, the bath is operated at ~0F and an external voltage of 12 volts is applied. If the coating thickness exceeds 0.5 microns, there is a tendency for the lead to bridge between individual filaments.
By the general procedure of Example 1, and sub-stituting a conventional gold bath for the nickel electro-plating bath and applying sufficient external voltage,composite high strength fibers comprising gold on graphite fibers are obtained.
Silicon carbide filaments and boron fibers are coated with nickel by placing them in cathodic contact with a nickel plating bath of Example 1 and applying an external voltage of about 30 volts.
l~S6~S2 A composition is prepared by chopping the composite fibers of Example 1 into short lengths, 1/8" to 1" long, then thoroughly mixing with thermoplastic nylon polyamide in an extruder, and chopping the extrudate into molding pellets in accordance with conventional procedures. The pellets are injection molded into plaques 4" x 8" x 1/8" in size. The plaque is reinforced by the composite fibers. By virtue of the metal content, it also does not build up static charge, and it can act as an electrical shield in electronic assemblies.
Bundles of nickel plated graphite fibers of about one inch in length prepared according to the procedure of Example 1 are mixed 1:9 with uncoated graphite fibers and laid up into a non woven mat, at 1 oz./l sq. yard. The mat has a metal content of about 5% by weight of nickel and can be impregnated with thermo-setting resinvarnishes and consolided under heat and pressure into reinforced laminates having high strength and excellent electrical dissipation properties.
Long, nickel coated graphite yarns prepared by the gen-eral procedure of Example 1 are pultruded at a high rate with molten lead in an apparatus from which a 1/8" diameter rod issues in solidified form, run down through the center of which lies the nickel coated graphite fibers. The lead is alloyed to the nickel without complete solvency of the nickel and the nickel is well bonded to the graphite fibrils. This results in a translation of the physical *i.e. pulled through molten metal and coated therewith *~
~lZ5~SZ
strength of the graphite fibers through the nickel plating, nickel/lead interlayer to the lead matrix. A section of the rod is pulled in an apparatus to measure breaking strength. In com-parison with a lead rod of the same diameter, the breaking strength of the nickel coated graphite fibers of this invention is very much higher.
Many variations of the present invention will suggest themselves to those skilled in this art in light of the above, de-tailed description. For example, aluminum can be deposited from ethereal solutions. Some metals, e.g., tungsten, can be deposited from molten salt solutions, e.g., sodium tungstenate. The tow can be treated to remove metal from sections thereof, and thereby segmented structures are provided which have utility, for example, as electrical resistors. All such variations are within the full intended scope of the invention as defined in the appended claims.
YARNS AND TOWS COMPRISING HIGH
STRENGTH METAL COATED FIBERS, PROCESS FOR THEIR PRODUCTION, AND ARTICLES MADE THEREFROM
The present invention relates to continuous yarns and tows comprising high strength bundles of composite fibers compris-ing conductive semi-metallic cores coated with thin adherent layers of metals, to methods for their production, and to articles made from such yarns.
, ~2S6(~52 BACKGROUND OF THE INVENTION
Bundles of high strength fibers of non-metals and semi-metals, such as carbon, boron, silicon carbide, and the like, in the form of filaments, mats, cloths and chopped strands are known to be ~seful in reinforcing metals an~ organic polymeric materials. Articles com-prising metals or plastics reinforced with such fibers find wide-spread use in replacing heavier components made of lower strength conventional materials such as aluminum, steel, titanium, vinyl polymers, nylons, polyesters, etc., in aircraft, automobiles, office equipment, sporting goods, and in many other fields.
A common problem in the use of such fibers, and also glass, asbestos, and others, is a seeming lack of ability to translate the properties of the high strength fibers to the material to which ultimate and intimate con-tact is to be made.
The problem is manifested in a variety of ways:
for example, if a length of high strength carbon fiber yarn is enclosed lengthwise in the center of a rod formed from solidified molten lead, and the rod is pulled until broken, 25 the breaking strength will be less than expected from the rule of mixtures, and greater than that of a rod formed from lead alone, due to the mechanical entrapment of the fibers. The lack of reinforcement strength is entirely due to poor translation of strength between the carbon fibers and the 30 lead. The same thing happens if an incompatible high strength fiber is mixed with a plastic material. If some types of carbon fibers, boron fibers, silicon carbide fibers, and the like in the forms of strands, chopped strands, non-woven mats, felts, papers, etc. or woven fabrics are mixed 35 w;th or~anic Dolymeri~ substances. such as phenolics B
lZS6~S2 styrenics, epoxy resins, polycarbonates, and the like, or mixed into molten metals, such as lead, aluminum, titanium, etc., they merely fill them without providing any reinforce-ment, and in many cases even cause physical properties to deteriorate.
All of these problems are generally recognized now, after years of research, to result from the need to insure adequate bonding between the high strength fiber and the so-called matrix materlal, the metal or plastic sought to be reinforced. It is also known that bonding can be improved with careful attention to the surface layer on each~
macro-micro filament or fibril in the material selected for use. Glass filaments, for example, are flame cleaned and 15 then sized with a plastic-compatible organosilane to produce reinforcements uniquely suitable for plastics.
Such techni~ues do not work well with other fibrous materials and, for obvious reasons, are not suitable 20 for carbon fibers, which would not have surface texture, and which have different boundary layers.
High stength carbon fibers are made by heating polymeric fiber, e.g., acrylonitrile polymers or copolymers, 25 in two stages, one to remove volatiles and carbonize and another to convert amorphous carbon into crystalline carbon.
During such procedure, it is known that the carbon changes from amorphous to single crystal then orients into fibrils.
If the fibers are stretched during the graphitization, then 30 high strength fibers are formed. This is critical to the formation of the boundary layer, because as the crystals grow, there are formed high surface energies, as exemplified by incomplete bonds, edge-to-edge stresses, differences in morphology, and the like. It is also known that the new 35 carbon fibrils in this form can scavenqe nascent oxygen ~,,1~
,,,~' lZ56~S2 from the air7 and even organic materials, to produce non-carbon surface layers which are firmly and chemically bonded thereto, although some can be removed by solvent treating, and there are some gaps or open spaces in the boundary layers.
Not unlike the contaminants on uncleaned, unsized glass fila-ments, these boundary layers on carbon fibers are mainly responsib~e for failure to achieve reinforcement with plastics and metals.
Numerous unsuccessful attempts have been reported to provide such filaments, especially carbon filaments, in a form uniquely suitable for reinforcing metals and plastics.
Most have involved depositing layers of metals, especially nickel and copper as thin surface layers on the filaments.
Such a composite filament was then to be used in a plastic or metal matrix. The metals in the prior art procedures have been vacuum deposited, electrolessly deposited, and electro-lytically deposited, but the resulting composites were not suitable.
Vacuum deposition, e.g., of nickel, U.S. 4,132,828, made what appears to be a continuous coating, but really isn't because the vacuum deposited metal first touches the fibrils through spaces in the boundary layer, then grows outwardly like a mushroom, then joins away from the surface, as observed under a scannins electron microscope as nodular nucleation. If the fiber is twisted, such a coating will fall off. The low density non-crystalline deposit limits use.
Electroless nickel baths have also been employed to plate such fibers but again there is the same problem, the initial nickel or other electroless metal seeds only small spots through holes in the boundary layer, then new 35 metal grows up like a mushroom and joins into what looks --- 12~(3S2 like a contlnuous coating, but it too will fall off when the fiber is twisted. The intermetallic compound is very locally nucleated and this, too, limits use. In the case of both vacuum deposition and electroless deposition, the strength of the metal-to-core bond is always substantially less than one-tenth that of the tensile strength of the : metal deposit itself.
Finally, electroplating with nickel and other metals is also featured in reported attempts to provide carbon fibers with a metal layer to make them compatible with metals and plastics, e.g., R.V. Sara, U.S. 3,622,283.
Short lengths of carbon fibers were clamped in a battery clip, immersed in an electrolyte, and electroplated with lS nickel. When the plated fibers were put into a tin metal matrix, the fibers did not translate their strength to the matrix to the extent expected from the rule or mixtures.
When fibers produced by such a process are sharply bent, on the compression side of the bend there appear a number of 20 transverse cracks and on the tension side of the bend the metal breaks and flakes off. If the metal coating is mechanically stripped, and the reverse side is examined under a high-power microscope, there is either no replica or at best only an incomplete replica of the fibril, the 25 replica defined to the 40 angstrom resolution of the scan-ning electron microscope. The latter two observations are strongly suggestive that failure to reinforce the aluminum matrix was due to poor bonding between the carbon and the nickel plating. In these cases, the metal to core bond 30 strength is no greater than one-half of the tensile strength on at most 10% of the fibers, and substantially less than one-tenth on the remaining 90~.
It has now been discovered that if electroplating 35 is selected, and if a very high order of external voltage is ~l~S6~5~
applied, much higher than was thought to be achievable in the prior art, uniform, continuous adherent, thin metal coatings can be provided to reinforcing fibrils, especially carbon fibrils. The voltage must be high enough to provide energy sufficient to push the metal ions through the boundary layer to provide uniform nucleation with the fibrils directly.
Composites of yarns or tows comprising the thin metal coat-ings on fibers, woven cloth, yarns, and the like, according to this invention can be knotted and folded without the metal flaking off. The composites are distinguishable from any of the prior art because they can be sharply bent without the fibrils slipping through a tube of the metal, as observed with electroless metal or vacuum deposited composites and sharply bending them, especially with nickel, produces - 15 neither transverse cracking ("alligatoring") on the compres-sion side of the bend nor breaking and flaking when the elastic limit of the metal is exceeded on the tension side - of the bend. In other words, the composites of the present invention are distinguishable from those of the prior art 20 because (i) they are continuous, (ii) the majority of the composite fibers are uniformly metal coated; and (iii) the bond strength (metal-to-core) on the majority of fibers is at least about 10 percent of the tensile strength of the metal deposit, preferably not substantially less than about 25 per-25 cent, especially preferably not substantially less than about50 percent. In the most preferred embodiments, the metal-to-core bond strength will be not substantially less than about 90 percent of the tensile strength of the metal deposit.
Highest properties will be achieved with yarns or tows of 30 composite fibers in which the metal-to-core bond strength approaches about 99 percent of the tensile strength of the metal, and special mention is made of these.
Articles made by adding the yarns or tows of the 35 present invention to a matrix forming material also dis-110-014 12~6~52 tinguish from the prior art because they are strongly reinforced. In addition, th~ articles possess other advantages, for example, they dissipate electrical charges and if certain innocuous metals are used in the coatings, e.g., gold and platinum, they will not be rejected when im-planted into the body.
' 10 ~ZS~S~
BRIEF DESCRIPTION OF THE DRAWINGS
The invention may be more readily understood by reference to the accompanying drawings in which:
Fig. 1 is a transverse cross sectional view of a metal coated fiber of this invention.
Fig. la is a longitudinal cross sectional view of a metal fiber according to this invention.
Fig. 2 and 2a are transverse cross sectional views of, respectively, a multinodal core and a "cracked"
core fiber coated with metal according to this invention.
Fig. 3 shows a longitudinal cross section of sharply bent metal coated fiber according to this invention;
and Fig. 3a shows a longitudinal cross section of a sharply bent metal coated composite prepared according to the prior art;
Fig. 4 is a partial sectional view of a metal coated composite fiber-reinforced polymer obtained by using this invention; and Fig. 5 is a view showing an apparatus for carry-ing out the process of the present invention.
All the drawings represent models of the articles described.
~25~52 SUMMARY OF THE INVENTION
In this disclosure the following terms are used with the following ~eanings:
fiber - the untreated material employed in the process of the invention to produce composite fiber composite fiber - metal-coated fiber of the invention core - central portion of the composite fiber (derived from the fiber) metal layer - the outer metal portion of the composite fiber.
(or layer) According to the present invention, there is provided a continuous yarn or tow comprising high strength composite fibers, the majority of which have an electrically conductive semi-metallic core and at least one thin, uniform and firmly adherent, electrically conductive layer of at least one metal on said core. Preferably the bond strength of said layer to said core being not substantially less than about 10 percent of the tensile strength of the metal. The bond strength of the layer to the core preferably is at least sufficient to provide that when the composite fiber is bent sharply enough to break the layer on the tension side of the bend because its elastic limit is exceeded, the layer on the compression side of the bend will remain bonded to the core and will not crack circumferentially.
Preferably the continuous yarn or tow can be knotted without substantial separation and loss of the metal layer.
In preferred features the core comprises carbon, boron or silicon carbide, especially carbon fibrils.
The most preferred yarns of composite fibers will be 1~56Q5Z
those in which, when the coating is removed by mechanical means and examined, there will be a replica of the fiber or fibril surface on the innermost surface of the removed coating, as examined under a scanning electron microscope of a definition of 40 angstroms or better.
Among the features of the invention are knottable tows or yarns of the new composite fibers, fabrics woven from such yarns (alone or with yarns which are of different material), non-woven sheets, mats and papers laid up from such fibers, chopped strands of such fibers and articles comprising such fibers uniformly dispersed in a matrix comprising a metal or an organic polymeric material. In preferred embodiments, coating metals will be nickel, silver, zinc, copper, lead, arsenic, cadmium, tin, cobalt, gold, indium, iridium, iron, palladium, platinum, tellurium, tungsten or a mixture of any of the fore-going, without limitation, preferably in crystalline form.
The invention further provides a continuous yarn or tow comprising high strength composite fibers, the majority of which have an electrically conductive semi-metallic substantially undegraded core and at least one thin, uniform and firmly adherent, electrically conductive layer of at least one metal on said core. Preferably the metal is a high voltage electrodeposited metal. Particularly preferred is a continuous yarn or tow of this type wherein the layer has been electrodeposited in an electro-deposition bath at an applied external voltage in excess of 10 volts while maintaining the yarn or tow cool enough outside the bath to prevent degradation of the continuous fibers.
12S~52 ~ 61109-7188 In another principal aspect of the present invention there is provided a process for the production of a continuous yarn or tow of high strength composite fibers having a fiber core and at least one thin, uniform, and firmly adherent electrically conductive layer of at least on~ metal adhered thereto; said process comprising:
(a) providing a continuous length of a plurality of electrically conductive semi-metallic fibers;
(b) continuously immersing at least a portion of the 10 length of said fibers in a bath capable of electrolytically depositing at least one metal thereon, (c) applying an external voltage in excess of 10 volts, (d) maintaining said voltage and resulting current, for a time sufficient to produce composite fibers comprising a thin, uniform, firmly adherent, electrically conductive layer of electrolytically deposited metal on said fibers each said fiber forming a core of each said composite fiber, (e) cooling the composite fibers as they leave the bath, for a time sufficient to prevent degradation of the said composite fibers, and (f) forming a yarn or tow from said composite fibers.
Preferably the applied external voltage is between 10 and 50 volts particularly between 12 and 36 volts and especially in excess of 13 volts.
In preferred features, the process will use core fibers of carbon, boron or silicon carbide, especially carbon fibrils.
Preferably the composite fibers are maintained cool enough by means outside the bath so that degradation is substant--lla- 61109-7188 ially avoided by recycling the liquid contents of the bath into contact with the fiber prior to immersion therein and with the composite fibers immediately subsequent to immersion therein.
A further aspect of the invention provides a process for preparing a reinforced composite which comprises intimately - contacting a liquid metal or a liquid organic material with at least a reinforcing amount of a fabric, a non-woven sheet or a chopped yarn, each as described above. Such a reinforced compos-ite thereby produced preferably forms a reinforced electrostati-cally shielded composite.
''0-014 _12 _ DETAILED DESCRIPTION OF THE INVENTION
Referring to Figs. 1 and la continuous yarns and tows for use in the core 2 according to the present invention are available from a number of sources commercially. For example, suitable carbon fiber yarns are available from Hercules Company, Hitco, Great Lakes Carbon Company, AVCO
Company and similar sources in the United States, and overseas. All are made, in general, by procedures des-10 cribed in U.S. 3,677,705. The fibers can be long and con-tinuous or they can be short, e.g., 1 to 15 cm. in length.
As mentioned above, all such carbon fibers will contain a thin, imperfect boundary layer (not shown) of chemically bonded oxygen and chemically or mechanically bonded other materials, such as organics.
Metal layer 4 will be of any electrodepositable metal, and it will be electrically continuous. Two layers, or even more, of metal can be applied and metal can be the same or different, as will be shown in the working examples.
In any case, the innermost layer will be so firmly bonded to core 2 that sharp bending will neck the metal down as shown in Fig. 3, snapping the fiber core and breaking the metal on the tension side of the bend when its elastic limit is exceeded. This is accomplished without causing the metal to flake off when broken (Fig. 3a), which is a problem in fibers metal coated according to the prior art.
As a further distinction from the prior art, the metal layer of the present invention fills interstices and "cracks" in fibers, uniformly and completely, as illustrated in Figs. 2 and 2a.
The high strength metal coated fibers of this invention can be assembled by conventional means into com-posites represented in Fig. 5 in which matrix 6 is a 1~ 014 1~'~6~SZ
_ 13 -o plastic, e.g., epoxy resin, or a metal, e.g., lead, the matrix being reinforced by virtue of the presence of high strength fibrous cores 2.
Formation of the metal coating layer by the electrodeposition process of this invention can be carried out in a number of ways. For example, a plurality of core fibers can be immersed in an electrolytic bath and through suitable electrical connections the required high external voltage can be applied. In one manner of proceeding, a high order of voltage is applied for a short period of time.
A pulse generator, for example, will send a surge of voltage through the electrolyte, sufficient to push or force the metal ion through the boundary layer into contact with the carbon or other fiber comprising the cathode. The short time elapsing in the pulse will prevent heat from building up in the fiber and burning it up or out. Because the fibers are so small, e.g., 5 to 10 microns in diameter, and because the innermost fibers are usually surrounded by hundreds or even thousands of others, even though only 0.5 to 2.6 volts are needed to dissociate the electrolytic metal ion, e.g., nickel, gold, silver, copper, depending on the salt used, massive amounts of external voltage are needed, of the order of 5 times the dissociation values, to uniformly nucleate the ions through the bundle of fibers into the innermost fibril and then through the boundary layer. Mini-mum external voltages of e.g., lO to 50, or even more, volts - are necessary.
Although pulsing as described above is suitable for small scale operations, for example, to metallize pieces of woven fabrics, and small lengths of carbon fiber yarns or tows, it is preferred to carry out the procedure in a continuous fashion on a moving tow of fibers. To over-come the problem of fiber burnout because of the high voltages, lZ5~(~52 to keep them cool enough outside the bath, one can separate the fibers and pour water on them,for example, but it is preferred to operate in an apparatus shown schematically in Figure 5. Electro-lytic bath solution 8 is maintained in tank 10. Also included are anode baskets 12 and idler rolls 14 near the bottom of tank 10.
Two electrical contact rollers 16 are located above the tank. Tow 24 is pulled by means not shown off feed roll 26, over first con-tact rol-ler 16 down into the bath under idler rolls 14, up through the bath, over second contact roller 16 and into take up roller 28. By way of illustration, the immersed tow length is about 6 feet. Optional, but very much preferred, is a simple loop compris-ing pump 18, conduit 20, and feed head 22. This permits recircu-lating the plating solution at a large flow rate, e.g., 2-3 gallons/
min. and pumping it onto contact rolls 16. Discharged just above the rolls, the sections of tow 24 leaving the solution are totally bathed with recirculated electrolyte, thus cooling them.
At the high current carried by the tow fibers, the I2R heat gener-ated in some cases might destroy them before they reach or after they leave the bath surface without such cooling. The flow of the electrolyte overcomes anisotropy. Of course, more than one plating bath can be used in series, and the fibers can be rinsed free of electrolyte solution, treated with other conventional materials and dried, chopped, woven into fabric, all in accordance with conventional procedures.
~' ., ,, ~ .
~2S6(~S2 - 15 _ DESCRIPTION OF THE PREFERRED EMBODIMENTS
The following Examples illustrates the present invention, but are not intended to limit it.
In a continuous electroplating system, a bath is provided having the following composition:
Ingredient Amount -nickel sulfate (NiSO4.6~2O) 40 ounces/gallon nickel chloride (NiC12.6H2O) 12 20 ounces/gallon boric acid (H3BO3) 5-8 ounces/gallon wetting agent (WA-129*, State 2% by volume Chemical) brightener (Starlite 915, State 2% by volume Chemical) The bath is heated to 140-160F and has a pH of 3.8-4.2.
The anode baskets are kept filled with electrolytic nickel pellets and 4 tows (fiber bundles) of 12,000 strands each of 7 micron carbon fibers are continuously drawn through the bath while an external voltage of 30 volts is applied at a current adjusted to give 10 ampere-minutes per 1000 strands total. At the same time,electrolytic solution is recycled through a loop into contact with the entering and leaving parts of the tow. The tow is next passed continuously through an identical bath, at a tow speed of 5.0 ft./min.
with 180 amps. current in each bath. The final product is a tow of high strength composite fibers according to this invention comprising a 7 micron fiber core and`about 50% by weight of the composite of crystalline electrodeposited nickel * I'rademark 110-014 1~56~S~
adhered firmly to the core.
If a length of the fi~er is sharply bent, then examined, there is no circumferential cracking on the metal coating in the tension side of the bend. The tow can be twisted and knotted without causing the coating to flake or come off as a powder. If a section of the coating is mechanically stripped from the fibrils, there will be a perfect reverse image (replica) on the reverse side. -If the procedure of Example 1 is repeated,substituting two baths of the following compositions, in series, and using silver in the anode baskets, silver coated graphite fibers according to this invention will be obtained.
Ingredient First BathSecond Bath Silver Cyanide 0.1-0.3 oz./gal.7-11 oz./gal.
Potassium Cyanide 12 - 20 oz./gal.12 oz./gal.
Potassium Hydroxide - - - 1- 2 oz./gal.
The first bath is to be operated at room tempera-ture and 12-36 volts; the second at room temperature and 6-18 volts.
The procedure of Example 2 can be modified, by substituting nickel plated graphite fibers as prepared in Example 1 for the feed, and the voltage in the first bath is reduced to about 18 volts. There are obtained high strength composite fibers according to this invention in 110-014 ~256~S2 which a silver ccating surrounds a nickel coating on a graphite fiber core.
The procedure of Example 1 can be modified by substituting for the nickel bath a bath of the following composition, using zinc in the anode baskets, and zinc coated graphite fibers according to this invention will be obtained:
Ingredient Amount Zinc sulfate 8 oz./gal.
Ammonium alum 3-4 oz./gal.
Potassium hydroxide 16 oz./gal.
Potassium cyanide 3 oz./gal.
The bath is run at 100F and 18 volts are externally applied.
The procedure of Example 1 can be modified by substituting for the nickel bath a bath of the following composition, using copper in the anode baskets, and copper coated graphite fibers according to this invention will be obtained:
Ingredient Amount Copper cyanide 3.5 oz./gal.
Sodium cyanide ~4.6 oz./gal.
Sodium carbonate 4 oz./gal.
Sodium hydroxide 0.5 oz./aal.
Rochelle salt 6 oz./gal.
.
The bath is run at 140F and 18 volts are externally applied. The copper plated fibers should be washed with sodium dichromate solution immediately after plating to prevent tarnishing. If the procedure of Example 3 is repeated, substituting the copper bath of this example for the silver bath, there will be obtained high strength composite fibers according to this invention in which a copper coating surrounds a nickel coating on a graphite fiber core.
The procedure of Example 1 can be modified by substituting for the nickel bath two baths of the following composition, using standard 80% cut20~ zinc anodes, and brass coated graphite fibers according to this invention will be obtained:
Ingredient Amount Copper cyanide4 oz./gal.
Zinc cyanide1.25 oz./gal.
Sodium cyanide7.5 oz./gal.
Sodium carbonate4 oz./gal.
Both baths are run at 110-120F. Since one-third of the brass is plated in the first bath, at 24 volts, and two-thirds in the second at 15 volts, the current is pro-portioned accordingly. Following two water rinses, the 30 brass plated fibers are washed with a solution of sodium dichromate, to prevent tarnishing, and then rinsed twice again with water.
lZ56~S2 The procedure of Example 1 can be modified by substituting for the nickel bath a bath of the following composition, using solid lead bars in the anode baskets, and lead coated graphite fibers according to this inven-tion wilI be obtained:
Inqredient Amount Lead fluoborate, Pb(BF4)2 14 oz. Pbtga Fluoboric acid, HBF4 13 oz./gal.
Optionally, about 2 g./l. each of ~-naphthol and of gelatine are added. The pH is less than 1, the bath is operated at ~0F and an external voltage of 12 volts is applied. If the coating thickness exceeds 0.5 microns, there is a tendency for the lead to bridge between individual filaments.
By the general procedure of Example 1, and sub-stituting a conventional gold bath for the nickel electro-plating bath and applying sufficient external voltage,composite high strength fibers comprising gold on graphite fibers are obtained.
Silicon carbide filaments and boron fibers are coated with nickel by placing them in cathodic contact with a nickel plating bath of Example 1 and applying an external voltage of about 30 volts.
l~S6~S2 A composition is prepared by chopping the composite fibers of Example 1 into short lengths, 1/8" to 1" long, then thoroughly mixing with thermoplastic nylon polyamide in an extruder, and chopping the extrudate into molding pellets in accordance with conventional procedures. The pellets are injection molded into plaques 4" x 8" x 1/8" in size. The plaque is reinforced by the composite fibers. By virtue of the metal content, it also does not build up static charge, and it can act as an electrical shield in electronic assemblies.
Bundles of nickel plated graphite fibers of about one inch in length prepared according to the procedure of Example 1 are mixed 1:9 with uncoated graphite fibers and laid up into a non woven mat, at 1 oz./l sq. yard. The mat has a metal content of about 5% by weight of nickel and can be impregnated with thermo-setting resinvarnishes and consolided under heat and pressure into reinforced laminates having high strength and excellent electrical dissipation properties.
Long, nickel coated graphite yarns prepared by the gen-eral procedure of Example 1 are pultruded at a high rate with molten lead in an apparatus from which a 1/8" diameter rod issues in solidified form, run down through the center of which lies the nickel coated graphite fibers. The lead is alloyed to the nickel without complete solvency of the nickel and the nickel is well bonded to the graphite fibrils. This results in a translation of the physical *i.e. pulled through molten metal and coated therewith *~
~lZ5~SZ
strength of the graphite fibers through the nickel plating, nickel/lead interlayer to the lead matrix. A section of the rod is pulled in an apparatus to measure breaking strength. In com-parison with a lead rod of the same diameter, the breaking strength of the nickel coated graphite fibers of this invention is very much higher.
Many variations of the present invention will suggest themselves to those skilled in this art in light of the above, de-tailed description. For example, aluminum can be deposited from ethereal solutions. Some metals, e.g., tungsten, can be deposited from molten salt solutions, e.g., sodium tungstenate. The tow can be treated to remove metal from sections thereof, and thereby segmented structures are provided which have utility, for example, as electrical resistors. All such variations are within the full intended scope of the invention as defined in the appended claims.
Claims (36)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A continuous yarn or tow comprising high strength composite fibers, the majority of which have an electrically conductive semi-metallic core and at least one thin, uniform and firmly adherent, electrically conductive layer of at least one metal on said core.
2. A continuous yarn or tow as defined in Claim 1 wherein said core comprises carbon.
3. A continuous yarn or tow as defined in Claim 1 which can be knotted without substantial separation and loss of said metal layer.
4. A continuous yarn or tow as defined in Claim 1 wherein the bond strength of said layer to said core in the majority of said composite fibers is at least sufficient to provide that when the composite fiber is bent sharply enough to break the layer on the tension side of the bend because its elastic limit is exceeded, the layer on the compression side of the bend will remain bonded to the core and will not crack circumferentially.
5. A continuous yarn or tow as defined in Claim 1 wherein said metal comprises nickel, silver, zinc, copper, lead, arsenic, cadmium, tin, cobalt, gold, indium, iridium, iron, palladium, platinum, tellurium, tungsten, or a mixture of any of the foregoing.
6. A continuous yarn or tow comprising high strength composite fibers, the majority of which have an electrically conductive semi-metallic substantially undegraded core and at least one thin, uniform and firmly adherent, electrically con-ductive layer of at least one metal on said core.
7. A continuous yarn or tow as defined in Claim 6 wherein said metal is a high voltage electrodeposited metal.
8. A continuous yarn or tow as defined in Claim 7 wherein said layer has been electrodeposited in an electrodeposition bath at an applied external voltage in excess of 10 volts while main-taining the yarn or tow cool enough outside the bath to prevent degradation of the said composite fibers.
9. A continuous yarn or tow as defined in Claim 8 wherein the composite fibers can be knotted without separation of the layer of metal or portions thereof from the core.
10. A continuous yarn or tow as defined in Claim 8 wherein the bond strength of said layer to said core in the majority of said composite fibers is at least sufficient to provide that when the composite fiber is bent sharply enough to break the layer on the tension side of the bend because its elastic limit is exceeded, the layer on the compression side of the bend will remain bonded to the core and will not crack circumferentially.
11. A fabric woven or knitted from yarns as defined in Claim 1, alone, or in combination with yarns which are of different material.
12. A non-woven sheet laid up from lengths of yarns as defined in Claim 1, alone, or in combination with yarns of different material.
13. A three-dimensional article of manufacture produced by weaving, knitting or laying up a mat comprised of yarns as defined in Claim 1, alone, or in combination with yarns of different material.
14. A composition of matter comprising yarns or tows as defined in Claim 1, disposed in a matrix comprising metal or an organic polymeric material.
15. A process for the production of a continuous yarn or tow of high strength composite fibers having a fiber core and at least one thin, uniform, and firmly adherent electrically conductive layer of at least one metal adhered thereto; said process comprising:
(a) providing a continuous length of a plurality of elec-trically conductive semi-metallic fibers;
(b) continuously immersing at least a portion of the length of said semi-metallic fibers in a bath capable of electrolytically depositing at least one metal thereon, (c) applying an external voltage in excess of 10 volts, (d) maintaining said voltage and resulting current, for a time sufficient to produce composite fibers comprising a thin, uniform, firmly adherent, electrically conductive layer of elec-trolytically deposited metal on said semi-metallic fibers each said semi-metallic fiber forming a core of each said composite - 24a -fiber, (e) cooling the composite fibers as they leave the bath, for a time sufficient to prevent degradation of the said composite fibers, and (f) forming a yarn or tow from said composite fibers.
(a) providing a continuous length of a plurality of elec-trically conductive semi-metallic fibers;
(b) continuously immersing at least a portion of the length of said semi-metallic fibers in a bath capable of electrolytically depositing at least one metal thereon, (c) applying an external voltage in excess of 10 volts, (d) maintaining said voltage and resulting current, for a time sufficient to produce composite fibers comprising a thin, uniform, firmly adherent, electrically conductive layer of elec-trolytically deposited metal on said semi-metallic fibers each said semi-metallic fiber forming a core of each said composite - 24a -fiber, (e) cooling the composite fibers as they leave the bath, for a time sufficient to prevent degradation of the said composite fibers, and (f) forming a yarn or tow from said composite fibers.
16. A process as defined in Claim 15 wherein the bond strength of said layer to said core in the majority of said composite fibers is at least sufficient to provide that when a composite fiber is bent sharply enough to break the coating on the tension side of the bend because its elastic limit is exceeded, the layer on the compression side of the bend will remain bonded to the core and will not crack circumferentially.
17. A process as defined in Claim 15 wherein said metal is crystalline.
18. A process as defined in Claim 15 wherein said core comprises carbon, boron or silicon carbide.
19. A process as defined in Claim 15 wherein said core comprises carbon.
20. A process as defined in Claim 15 wherein the product of the process is a tow or yarn of composite fibers which can be knotted without separation of the layer of metal or portions thereof from the core of said composite fibers.
21. A process as defined in Claim 15 including the step of weaving or knitting yarn produced by the process alone, or in combination with yarn of a different material into a fabric.
22. A process as defined in Claim 15 including the step of laying up the yarn produced by the process alone, or in com-bination with yarn or a different material into a non-woven sheet.
23. A process as defined in either of Claims 21 or 22 including the further step of converting the woven, knitted, or laid-up material into a three-dimensional article of manufacture.
24. A process as defined in Claim 15 including the step of chopping the yarn produced by the process into shortened lengths.
25. A process for forming a reinforced composite which comprises intimately contacting a liquid metal or a liquid organic polymeric material with at least a reinforcing amount of (a) a fabric produced according to Claim 21; or (b) a non-woven sheet produced according to Claim 22; or (c) chopped yarn produced according to Claim 24.
26. A composition of matter comprising a reinforced com-posite produced by intimately contacting a liquid metal or a liquid organic polymeric material with an amount of yarn, sheet or chopped fibers prepared according to Claim 21, 22 or 24, wherein the amount of yarn, sheet or chopped fibers is sufficient to provide a reinforced electrostatically shielded composite.
27. A process as defined in Claim 15 wherein the applied external voltage is between 10 and 50 volts.
28. A process as defined in Claim 27 wherein the applied external voltage is between 12 and 36 volts.
29. A process as defined in Claim 28 wherein the applied external voltage is in excess of 13.0 volts.
30. A process as defined in Claim 15 wherein the composite fibers are maintained cool enough by means outside the bath so that degradation is substantially avoided, comprising recycling liquid contents of the bath into contact with the semi-metallic fiber prior to immersion therein and with the composite fibers immediately subsequent to immersion therein.
31. A process as defined in Claim 30 wherein the applied external voltage is in the range of 10 to 50 volts.
32. A process as defined in Claim 31 wherein the applied external voltage is in the range of 12 to 36 volts.
33. A process as defined in Claim 32 wherein the applied external voltage is in excess of 13.0 volts.
34. A process as defined in Claim 30 wherein the bond strength of said layer to said core in the majority of said composite fibers is at least sufficient to provide that when a composite fiber is bent sharply enough to break the layer on the tension side of the bend because its elastic limit is exceeded, the layer on the compression side of the bend will remain bonded to the core and will not crack circumferentially.
35. A process as defined in Claim 30 wherein said metal is crystalline.
36. A process as defined in Claim 30 wherein the product of the process is a tow or yarn of composite fibers which can be knotted without separation of the layer of metal or portions thereof from the core of said composite fibers.
Applications Claiming Priority (2)
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US35863782A | 1982-03-16 | 1982-03-16 | |
US358,637 | 1989-05-30 |
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CA000423551A Expired CA1256052A (en) | 1982-03-16 | 1983-03-14 | Tows and yarns of high strength electroplated carbon fibers |
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IL (1) | IL67867A (en) |
IN (1) | IN158302B (en) |
MX (1) | MX159077A (en) |
NO (1) | NO164996C (en) |
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IL67867A (en) * | 1982-03-16 | 1987-10-30 | Electro Metalloid Corp | Yarns and tows comprising high strength metal coated fibers,process for their production and articles made therefrom |
EP0129845B1 (en) * | 1983-06-24 | 1988-10-26 | American Cyanamid Company | Electrodes, electro-chemical cells containing said electrodes, and process for forming and utilizing such electrodes |
DE3482273D1 (en) * | 1983-06-24 | 1990-06-21 | American Cyanamid Co | DEVICE AND METHOD FOR CONTINUOUSLY PLATING FIBERS. |
EP0149763A3 (en) * | 1983-11-29 | 1985-08-21 | Toho Beslon Co., Ltd. | Electroplating method for carbon fibers and apparatus therefor |
FR2562101B1 (en) * | 1984-03-27 | 1987-03-06 | Brochier Sa | MATERIAL BASED ON INORGANIC FIBERS, PARTICULARLY SILICON CARBIDE, FOR USE IN THE PRODUCTION OF COMPOSITE STRUCTURES |
EP0269850A1 (en) * | 1986-10-31 | 1988-06-08 | American Cyanamid Company | Copper coated fibers |
ATE73010T1 (en) * | 1988-10-12 | 1992-03-15 | Johnson Matthey Plc | METAL FABRIC. |
CA2125378A1 (en) * | 1993-06-09 | 1994-12-10 | James A. E. Bell | Composition for lightning strike protection and improved electrical conductivity |
JP2002180372A (en) * | 2000-12-15 | 2002-06-26 | Toho Tenax Co Ltd | Carbon fiber coated with metal oxide and method for producing the same |
JP7032348B2 (en) * | 2019-03-26 | 2022-03-08 | 矢崎総業株式会社 | Metal-plated carbon material and its manufacturing method |
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GB1215002A (en) * | 1967-02-02 | 1970-12-09 | Courtaulds Ltd | Coating carbon with metal |
FR1535660A (en) * | 1967-06-28 | 1968-08-09 | Thomson Houston Comp Francaise | Improvements in manufacturing processes for composite materials and products obtained |
IL67867A (en) * | 1982-03-16 | 1987-10-30 | Electro Metalloid Corp | Yarns and tows comprising high strength metal coated fibers,process for their production and articles made therefrom |
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1983
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- 1983-02-08 EP EP83101195A patent/EP0088884B1/en not_active Expired
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- 1983-03-11 JP JP58039306A patent/JPS58169532A/en active Pending
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- 1983-03-14 ES ES520574A patent/ES520574A0/en active Granted
- 1983-03-14 CA CA000423551A patent/CA1256052A/en not_active Expired
- 1983-03-15 NO NO830897A patent/NO164996C/en unknown
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- 1983-03-15 DK DK120683A patent/DK158159C/en not_active IP Right Cessation
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1987
- 1987-04-03 AU AU71081/87A patent/AU588991B2/en not_active Ceased
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1991
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DK158159C (en) | 1990-08-27 |
ES8406576A1 (en) | 1984-08-01 |
DK120683D0 (en) | 1983-03-15 |
IL67867A0 (en) | 1983-06-15 |
AU1245083A (en) | 1983-09-22 |
ES520574A0 (en) | 1984-08-01 |
EP0088884B1 (en) | 1986-09-10 |
IL67867A (en) | 1987-10-30 |
BR8301227A (en) | 1983-11-22 |
AR240342A1 (en) | 1990-03-30 |
AU588991B2 (en) | 1989-09-28 |
KR880000477B1 (en) | 1988-04-07 |
KR840004193A (en) | 1984-10-10 |
FI830854L (en) | 1983-09-17 |
DK120683A (en) | 1983-09-17 |
HK14491A (en) | 1991-03-08 |
NO164996C (en) | 1990-12-05 |
NO830897L (en) | 1983-09-19 |
FI75876C (en) | 1988-08-08 |
ATE22121T1 (en) | 1986-09-15 |
FI830854A0 (en) | 1983-03-15 |
IN158302B (en) | 1986-10-11 |
EP0088884A1 (en) | 1983-09-21 |
FI75876B (en) | 1988-04-29 |
AU7108187A (en) | 1987-07-23 |
NO164996B (en) | 1990-08-27 |
JPS58169532A (en) | 1983-10-06 |
AU561667B2 (en) | 1987-05-14 |
MX159077A (en) | 1989-04-14 |
DK158159B (en) | 1990-04-02 |
DE3365941D1 (en) | 1986-10-16 |
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