JPS623527B2 - - Google Patents
Info
- Publication number
- JPS623527B2 JPS623527B2 JP16302378A JP16302378A JPS623527B2 JP S623527 B2 JPS623527 B2 JP S623527B2 JP 16302378 A JP16302378 A JP 16302378A JP 16302378 A JP16302378 A JP 16302378A JP S623527 B2 JPS623527 B2 JP S623527B2
- Authority
- JP
- Japan
- Prior art keywords
- lubricant
- wire
- melting point
- insulated wire
- acid
- 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
- 239000000314 lubricant Substances 0.000 claims description 78
- 238000002844 melting Methods 0.000 claims description 52
- 230000008018 melting Effects 0.000 claims description 52
- 239000007787 solid Substances 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 26
- 238000010438 heat treatment Methods 0.000 claims description 21
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 230000001050 lubricating effect Effects 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 230000003068 static effect Effects 0.000 claims description 3
- 239000012188 paraffin wax Substances 0.000 description 29
- 239000002904 solvent Substances 0.000 description 21
- 235000019441 ethanol Nutrition 0.000 description 20
- 150000001298 alcohols Chemical class 0.000 description 16
- 235000014113 dietary fatty acids Nutrition 0.000 description 16
- 229930195729 fatty acid Natural products 0.000 description 16
- 239000000194 fatty acid Substances 0.000 description 16
- 150000004665 fatty acids Chemical class 0.000 description 16
- 238000004804 winding Methods 0.000 description 13
- 238000000576 coating method Methods 0.000 description 11
- 229920006395 saturated elastomer Polymers 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 9
- 239000000155 melt Substances 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- UTOPWMOLSKOLTQ-UHFFFAOYSA-N octacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O UTOPWMOLSKOLTQ-UHFFFAOYSA-N 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- 239000001993 wax Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 239000010687 lubricating oil Substances 0.000 description 4
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 150000002763 monocarboxylic acids Chemical class 0.000 description 3
- YDLYQMBWCWFRAI-UHFFFAOYSA-N n-Hexatriacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC YDLYQMBWCWFRAI-UHFFFAOYSA-N 0.000 description 3
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 3
- GWVDBZWVFGFBCN-UHFFFAOYSA-N tetratriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC GWVDBZWVFGFBCN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- ONLMUMPTRGEPCH-UHFFFAOYSA-N Hentriacontanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O ONLMUMPTRGEPCH-UHFFFAOYSA-N 0.000 description 2
- LRKATBAZQAWAGV-UHFFFAOYSA-N Hexatriacontylic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O LRKATBAZQAWAGV-UHFFFAOYSA-N 0.000 description 2
- AJQRZOBUACOSBG-UHFFFAOYSA-N Octatriacontanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O AJQRZOBUACOSBG-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000002390 adhesive tape Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- HOWGUJZVBDQJKV-UHFFFAOYSA-N docosane Chemical compound CCCCCCCCCCCCCCCCCCCCCC HOWGUJZVBDQJKV-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- QHMGJGNTMQDRQA-UHFFFAOYSA-N dotriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC QHMGJGNTMQDRQA-UHFFFAOYSA-N 0.000 description 2
- ICAIHSUWWZJGHD-UHFFFAOYSA-N dotriacontanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O ICAIHSUWWZJGHD-UHFFFAOYSA-N 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 230000005183 environmental health Effects 0.000 description 2
- -1 ethyl alcohol Chemical class 0.000 description 2
- FNAZRRHPUDJQCJ-UHFFFAOYSA-N henicosane Chemical compound CCCCCCCCCCCCCCCCCCCCC FNAZRRHPUDJQCJ-UHFFFAOYSA-N 0.000 description 2
- CKDDRHZIAZRDBW-UHFFFAOYSA-N henicosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCC(O)=O CKDDRHZIAZRDBW-UHFFFAOYSA-N 0.000 description 2
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 2
- BJQWYEJQWHSSCJ-UHFFFAOYSA-N heptacosane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCC BJQWYEJQWHSSCJ-UHFFFAOYSA-N 0.000 description 2
- KEMQGTRYUADPNZ-UHFFFAOYSA-N heptadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(O)=O KEMQGTRYUADPNZ-UHFFFAOYSA-N 0.000 description 2
- PXEZIKSRSYGOED-UHFFFAOYSA-N heptatriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC PXEZIKSRSYGOED-UHFFFAOYSA-N 0.000 description 2
- HMSWAIKSFDFLKN-UHFFFAOYSA-N hexacosane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCC HMSWAIKSFDFLKN-UHFFFAOYSA-N 0.000 description 2
- XMHIUKTWLZUKEX-UHFFFAOYSA-N hexacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O XMHIUKTWLZUKEX-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- BTFJIXJJCSYFAL-UHFFFAOYSA-N icosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- IGGUPRCHHJZPBS-UHFFFAOYSA-N nonacosane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCC IGGUPRCHHJZPBS-UHFFFAOYSA-N 0.000 description 2
- IHEJEKZAKSNRLY-UHFFFAOYSA-N nonacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O IHEJEKZAKSNRLY-UHFFFAOYSA-N 0.000 description 2
- ISYWECDDZWTKFF-UHFFFAOYSA-N nonadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCCC(O)=O ISYWECDDZWTKFF-UHFFFAOYSA-N 0.000 description 2
- SNXOSZZZNFRFNZ-UHFFFAOYSA-N nonatriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC SNXOSZZZNFRFNZ-UHFFFAOYSA-N 0.000 description 2
- ZYURHZPYMFLWSH-UHFFFAOYSA-N octacosane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCC ZYURHZPYMFLWSH-UHFFFAOYSA-N 0.000 description 2
- BVKCQBBZBGYNOP-UHFFFAOYSA-N octatriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC BVKCQBBZBGYNOP-UHFFFAOYSA-N 0.000 description 2
- YKNWIILGEFFOPE-UHFFFAOYSA-N pentacosane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCC YKNWIILGEFFOPE-UHFFFAOYSA-N 0.000 description 2
- MWMPEAHGUXCSMY-UHFFFAOYSA-N pentacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCC(O)=O MWMPEAHGUXCSMY-UHFFFAOYSA-N 0.000 description 2
- VHQQPFLOGSTQPC-UHFFFAOYSA-N pentatriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC VHQQPFLOGSTQPC-UHFFFAOYSA-N 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- KUPLEGDPSCCPJI-UHFFFAOYSA-N tetracontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC KUPLEGDPSCCPJI-UHFFFAOYSA-N 0.000 description 2
- POOSGDOYLQNASK-UHFFFAOYSA-N tetracosane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC POOSGDOYLQNASK-UHFFFAOYSA-N 0.000 description 2
- OLTHARGIAFTREU-UHFFFAOYSA-N triacontane Natural products CCCCCCCCCCCCCCCCCCCCC(C)CCCCCCCC OLTHARGIAFTREU-UHFFFAOYSA-N 0.000 description 2
- VHOCUJPBKOZGJD-UHFFFAOYSA-N triacontanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O VHOCUJPBKOZGJD-UHFFFAOYSA-N 0.000 description 2
- FIGVVZUWCLSUEI-UHFFFAOYSA-N tricosane Chemical compound CCCCCCCCCCCCCCCCCCCCCCC FIGVVZUWCLSUEI-UHFFFAOYSA-N 0.000 description 2
- XEZVDURJDFGERA-UHFFFAOYSA-N tricosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCC(O)=O XEZVDURJDFGERA-UHFFFAOYSA-N 0.000 description 2
- SZHOJFHSIKHZHA-UHFFFAOYSA-N tridecanoic acid Chemical compound CCCCCCCCCCCCC(O)=O SZHOJFHSIKHZHA-UHFFFAOYSA-N 0.000 description 2
- 235000021357 Behenic acid Nutrition 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ROOBHHSRWJOKSH-UHFFFAOYSA-N Hentriacontan-1-ol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO ROOBHHSRWJOKSH-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000021353 Lignoceric acid Nutrition 0.000 description 1
- CQXMAMUUWHYSIY-UHFFFAOYSA-N Lignoceric acid Natural products CCCCCCCCCCCCCCCCCCCCCCCC(=O)OCCC1=CC=C(O)C=C1 CQXMAMUUWHYSIY-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229940053200 antiepileptics fatty acid derivative Drugs 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 235000019504 cigarettes Nutrition 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- KFEVDPWXEVUUMW-UHFFFAOYSA-N docosanoic acid Natural products CCCCCCCCCCCCCCCCCCCCCC(=O)OCCC1=CC=C(O)C=C1 KFEVDPWXEVUUMW-UHFFFAOYSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N heptadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- FUJXKFCTVKZXTJ-UHFFFAOYSA-N hexacosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCN FUJXKFCTVKZXTJ-UHFFFAOYSA-N 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- YAQXGBBDJYBXKL-UHFFFAOYSA-N iron(2+);1,10-phenanthroline;dicyanide Chemical compound [Fe+2].N#[C-].N#[C-].C1=CN=C2C3=NC=CC=C3C=CC2=C1.C1=CN=C2C3=NC=CC=C3C=CC2=C1 YAQXGBBDJYBXKL-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000010721 machine oil Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- IACKKVBKKNJZGN-UHFFFAOYSA-N n-Pentakosylalkohol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCO IACKKVBKKNJZGN-UHFFFAOYSA-N 0.000 description 1
- XGFDHKJUZCCPKQ-UHFFFAOYSA-N n-nonadecyl alcohol Natural products CCCCCCCCCCCCCCCCCCCO XGFDHKJUZCCPKQ-UHFFFAOYSA-N 0.000 description 1
- 231100000989 no adverse effect Toxicity 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- DZLRGXSUDHQIOZ-UHFFFAOYSA-N octacosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCN DZLRGXSUDHQIOZ-UHFFFAOYSA-N 0.000 description 1
- CNNRPFQICPFDPO-UHFFFAOYSA-N octacosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCO CNNRPFQICPFDPO-UHFFFAOYSA-N 0.000 description 1
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 1
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- REIUXOLGHVXAEO-UHFFFAOYSA-N pentadecan-1-ol Chemical compound CCCCCCCCCCCCCCCO REIUXOLGHVXAEO-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 229920003055 poly(ester-imide) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 150000003839 salts Chemical group 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003509 tertiary alcohols Chemical class 0.000 description 1
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 1
- QZZGJDVWLFXDLK-UHFFFAOYSA-N tetracosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC(O)=O QZZGJDVWLFXDLK-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- REZQBEBOWJAQKS-UHFFFAOYSA-N triacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO REZQBEBOWJAQKS-UHFFFAOYSA-N 0.000 description 1
- SUJUOAZFECLBOA-UHFFFAOYSA-N tritriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC SUJUOAZFECLBOA-UHFFFAOYSA-N 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B13/00—Apparatus or processes specially adapted for manufacturing conductors or cables
- H01B13/06—Insulating conductors or cables
- H01B13/16—Insulating conductors or cables by passing through or dipping in a liquid bath; by spraying
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/308—Wires with resins
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Manufacturing Of Electric Cables (AREA)
- Lubricants (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Description
【発明の詳細な説明】
本発明は捲線性のすぐれた潤滑性絶縁電線の製
造方法に関するものである。
近年、エナメル線を使用する電機メーカー等に
於ては、機器の製造工程の迅速化を図るため、高
速自動捲線機を使用するようになつて来ている。
しかし、この場合、工程の迅速化により機器の加
工費は著しく減少させることが出来たかに見受け
られるが、実際には捲線加工時エナメル線は摩擦
等をうけ、絶縁層が機械的損傷をうける。このた
め機器に組み込まれた後、レアーシヨートを起し
てロス率が大幅に増加するという大きな問題を有
している。これを解決するため、エナメル線に潤
滑性を付与し、機械的損傷を低減することが試み
られている。このことは自動捲線機のみならず手
作業においても同様であり、例えばモーターの狭
いスロツトにエナメル線を挿入する際、手作業の
能率を高めるためすべり性の良いエナメル線が要
望されている。
エナメル線自体は潤滑性に乏しいため、エナメ
ル線同志、エナメル線と捲線機間、エナメル線と
機器間等のすべりが悪く、絶縁層に損傷を受けた
り作業効率が悪くなつたりする。このため、エナ
メル線上に流動パラフイン、冷凍機油等の液体の
潤滑剤を塗布する方法が取られている。しかしな
がらこの方法は潤滑性、すべり性が不十分である
ため、手作業において線さばき性が悪く、又捲線
時にはトランス、コイル等の整列巻性が悪いとい
う難点があり、更に近年の高速捲線化、占積率向
上インサーター方式の適用拡大等によりレヤーシ
ヨートが増大している。又この方法は液体の潤滑
剤を使用するので、電線にゴミが付着しやすいば
かりでなくコイル捲後線のばらけや、端末止めの
ための粘着テープとか接着テープの粘着力、接着
力に悪影響を及ぼしテープがはがれ易いという欠
点もある。
この解決のため、コイル捲きを行う電機メーカ
ーでは例えば塊状の固形パラフインの上に電線を
通して電線表面に固形パラフインをこすりつける
方法をとる事もあるが、付着量が不均一でむらが
あり、一般に多すぎる事、電線が固形パラフイン
にすぐに喰い込んでゆきそのたびに取り替え、又
再生のために融解して後固化再生をたびたび繰返
す必要がある事、作業能率が低下する事等の欠点
があり、電線メーカーに対して用途、サイズに応
じて潤滑処理を行い、かつ用途、サイズ等に応じ
て潤滑剤の種類、量を変えるよう強く要望されて
いる。
これを受けて電線メーカーでは、例えばベンジ
ン、キシレン等の溶剤に固形パラフインを1%程
度溶解して電線表面に塗布或は塗布後加熱乾燥を
するという方法でやむなく対処しているのが現状
である。
しかしこの方法の場合、大部分が溶剤であるた
め大量の無駄になる溶剤を消費し、衛生、安全上
排気設備を必要とし公害対策上排出された溶剤の
燃焼等による除去設備を必要とし、かつ引火点の
低い溶剤を使用するため火災の危険性をはらんで
いる。又加熱乾燥を行う場合は加熱炉を必要とす
る。次に特性面よりみると、溶剤が電線表面に接
触した時電線品種によつてはクレージングを発生
し電線として商品価値がなくなるため適用品種が
限定され、又潤滑剤溶液は低濃度で非常に低粘度
であるため付着膜厚のコントロールは出来ずただ
電線が溶液中を通る時付着するにまかせるしかな
い。なお、固形パラフインは溶剤に対する溶解性
が悪く、溶剤の種類、濃度に大きな制約があり、
固形パラフイン以外の固体の有機潤滑剤をみて
も、ほとんどのものが溶剤に難溶もしくは不溶で
仮りに溶解しても低濃度である。従つて所望の固
体の有機潤滑剤を使おうとしても、溶剤に溶解し
ないため使用出来ないが、もしくは溶解した場合
でも低濃度でしか使えないという制約がある。
以上述べた通り溶液法は省資源、公害規制、環
境衛生、安全上、多くの不具合点を有し、かつ特
性適用範囲、適用潤滑剤の範囲の点でも制約条件
が多いのが現状である。
しかしながら需要家の要求にこたえないわけに
はゆかず矛盾点を包合しながら製造せざるを得な
いのが現状である。
本発明者らは、これら問題解決について鋭意検
討の結果本発明の方法に到達したものである。
本発明は、溶剤を使わず、常温で固体の有機潤
滑剤を加熱溶融してエナメル線上に塗布し潤滑性
のすぐれた絶縁電線を得るものである。
本発明では、常温で固体の有機潤滑剤を使用す
るので、液体潤滑剤を使用する場合に較べ滑り性
がよく、又電線にゴミが付着することなく、接着
テープの接着力に悪影響もなく、液体潤滑剤の問
題点を解決することが出来る。又本発明では溶液
法と同等以上の潤滑性絶縁電線が得られ、しかも
溶剤を使用しないので溶剤を消費せず省資源にな
り環境衛生、安全のための排気設備が必要なく、
公害対策のための排出溶剤の燃焼等の除去設備が
不要で、低引火点溶剤による火災の心配もない。
又当然ながら溶剤乾燥用の加熱炉も必要ない。
更に溶剤によるクレージングの心配がないので
適用品種の制限もない。又100%潤滑剤であるた
め粘度コントロール、温度コントロール、塗布
量、絞り量等のコントロールで自由に付着膜厚が
変えられる。
更に加熱溶融するため、溶液法では使用出来な
かつた溶剤に難溶もしくは不溶の潤滑剤が使用で
きる利点がある。
本発明で用いられる常温で固体の有機潤滑剤は
加熱時に溶融するものでかつ、エナメル線上に塗
布された後、固化し潤滑性を示すものであればい
かなるものでもよい。
潤滑剤としては長鎖の脂肪族基をもつた化合物
が好ましい。
脂肪族基は極性が小さく滑り性が良いからであ
る。脂肪族基には飽和と不飽和があるが、飽和の
方が極性が小さく好ましい。アルキル基が長けれ
ば長いほどその効果が発揮でき、特にアルキル基
の炭素数が21以上が好ましい。
アルキル基は、分岐したものより直鎖状の方が
滑りが良く好ましい。特にアルキル基の骨格の一
部が−(CH2−)oから成りn20が好ましい。
潤滑剤はその平均分子量が100以下が好まし
い。分子量が大きすぎると、溶融粘度が高く塗布
が困難になつたり融点又は軟化点が高すぎて熱分
解することがあり好ましくないからである。
次に本発明で用いられる潤滑剤の例をあげる。
各々の潤滑剤のなかで特に好ましいものは先に
述べたアルキル基の炭素数、アルキル基の骨格、
平均分子量等を満すものであることはいうまでも
ない。
例としては炭化水素、脂肪酸或はその誘導体、
アルコール或いはその誘導体、脂肪酸アミド或は
その誘導体、ワツクス類、グリース類、等があげ
られる。勿論これらの潤滑剤を混合して使用する
こともできる。
潤滑剤の更に具体的な例を次にあげる。
炭化水素は炭素数の大きいものが好ましいのは
いうまでもない。炭化水素には、飽和、不飽和の
ものがあり、又、直鎖状、分岐状のものがある
が、一般式CH3(CH2)oCH3で表わされる飽和で
直鎖状のものが好ましい。
この例としてヘンエイコサン、ドコサン、トリ
コサン、テトラコサン、ペンタコサン、ヘキサコ
サン、ヘプタコサン、オクタコサン、ノナコサ
ン、トリアコンタン、ヘントリアコンタン、ドト
リアコンタン、トリトリアコンタン、テトラトリ
アコンタン、ペンタトリアコンタン、ヘキサトリ
アコンタン、ヘプタトリアコンタン、オクタトリ
アコンタン、ノナトリアコンタン、テトラコンタ
ン、等がある。
又いわゆる固形パラフインとして市販されてい
る飽和で直鎖の炭化水素を主成分とする炭化水素
も好ましい。
次に脂肪酸或はその誘導体について例をあげ
る。脂肪酸は、炭素数の多いアルキル基をもつた
もの即ち、高級脂肪酸が好ましい。
高級脂肪酸には、飽和酸、不飽和酸があり、又
アルキル基が直鎖のもの分岐したものがある。又
官能基数によりモノカルボン酸、ジカルボン酸、
テトラカルボン酸などがある。この中でも一般式
CH3(CH2)oCOOHであらわされる直鎖飽和モノ
カルボン酸が最も好ましい。この理由は潤滑性の
効果を発揮するためには極性基が少ない方が良い
からである。
高級脂肪酸のうち最も好ましい直鎖飽和モノカ
ルボン酸の一例をあげると、ドデカン酸、トリデ
カン酸、テトラデカン酸、ペンタデカン酸、ヘキ
サデカン酸、ヘプタデカン酸、オクタデカン酸、
ノナデカン酸、エイコサン酸、ヘンエイコサン
酸、ドコサン酸、トリコサン酸、テトラコサン
酸、ペンタコサン酸、ヘキサコサン酸、ヘプタコ
サン酸、オクタコサン酸、ノナコサン酸、トリア
コンタン酸、ヘントリアコンタン酸、ドトリアコ
ンタン酸、テトラトリアコンタン酸、ヘキサトリ
アコンタン酸、オクタトリアコンタン酸、等があ
る。脂肪酸の誘導体として酸無水物、エステル、
塩などがある。エステルにはメチルアルコール、
エチアルコール等の一価アルコール、エチレング
リコール、ジエチレングリコール等の二価アルコ
ール、グリセリン、トリメチロールプロパン等の
三価アルコール、ペンタエリスリツト等の四価ア
ルコール等種々のアルコールとのエステルがあ
る。潤滑性付与のためには、脂肪族基が長い方が
好ましいので二価以上のアルコールとのエステル
が好ましい。又同じ理由で低級アルコールより高
級アルコールとのエステルが好ましい。
次にアルコール或はその誘導体の例を示す。ア
ルコールは、炭素数の多いアルキル基をもつたも
の即ち、高級アルコールが好ましい。
高級アルコールには飽和アルコール、不飽和ア
ルコールがあり又アルキル基が直鎖のもの、分岐
したものがある。又、官能基の位置により1級ア
ルコール、2級アルコール、3級アルコールがあ
り又官能基数により1価アルコール、2価アルコ
ール、3価アルコール等がある。
この中で最も好ましいのは、先に述べた理由か
ら一般式CH3(CH2)oOHで表わされる直鎖状飽
和の1級1価アルコールが好ましい。例として
は、ペンタデカン1−オール、ヘキサデカン1−
オール、ヘプタデカン1−オール、オクタデカン
1−オール、ノナデカン1−オール、エイコサン
1−オール、ヘンエイコサノール−1、ドコサノ
ール−1、テトラコサノール−1、ペンタコサノ
ール−1、ヘキサコサノール−1、ヘプタコサノ
ール−1、オクタコサノール−1、ノナコサノー
ル−1、トリアコンタノール−1、ヘントリアコ
ンタノール−1、ドトリアコンタノール−1、ト
リトリアコンタノール−1、テトラトリアコンタ
ノール−1、ペンタトリアコンタノール−1、ヘ
プタトリアコンタノール−1、等がある。
アルコールの誘導体として、カルボン酸とのエ
ステルがあるが、特に好ましいのは、先に述べた
高級脂肪酸とのエステルである。
次に脂肪酸アミド或その誘導体の例をあげる。
脂肪酸アミドは炭素数の多いアルキル基をもつた
もの、即ち高級脂肪酸アミドが好ましい。脂肪酸
アミドの骨格のうち炭化水素基は前述の脂肪酸で
述べたものがある。脂肪酸アミドの中で好ましい
のは、一般式CH3(CH2)oCONH2で表わされるも
のである。この例として、パルミチルアミド、ス
テアリルアミド、エイコシルアミド、ドコシルア
ミド、ヘキサコシルアミド、オクタコシルアミド
等がある。脂肪酸アミドの誘導体としては、アミ
ノ基の水素がアルキル基によつて置換されたもの
とか、一般式RCONH−CH2−NHCOR、RCONH
−CH2−CH2−NHCORで表わされるビス脂肪酸
アミドがある。
ワツクス類の例として、マイクロクリスタリン
ワツクス、カルナバロウ、ミツロウ、モンタンロ
ウ等がある。又モンタンワツクス酸をベースとし
た或は、その誘導体である、ヘキストジヤパン社
から販売されているヘキストワツクスOP(鎖長
C28〜32のモンタン酸からの部分ケン化エステル
ワツクス)、ヘキストワツクスE(モンタン酸か
らのエステルワツクス)、ヘキストワツクスS
(モンタン酸ワツクス)も好適である。
以上述べた潤滑剤の中で最も好ましいのは固形
パラフインである。固形パラフインは安価に容易
に入手することが出来るし、通常融点範囲毎に市
販されているので所望の融点のものが選択出来
る。又、化学的に安定で毒性もなく取扱いには好
適である。
本発明の特徴は、融点が56℃以下の有機潤滑剤
と融点が60℃以上の有機潤滑剤とを二種以上混合
して用いることである。
潤滑剤を単独で用いる場合、加熱温度は潤滑剤
の融点以上にしなければならないが、高い融点の
潤滑剤と低い融点の潤滑剤を混合して使用すれば
両者の融点の間の温度で溶融出来るので、加熱温
度範囲が広くなり加熱装置の温度制御幅が広く、
又溶融粘度も自由に選択出来る。
固形パラフインを例にとつて説明する。
固形パラフインは一般に融点範囲毎に市販され
ているが、異なる融点のものを混合して用いると
次のような利点がある。例えば融点54〜56℃の固
形パラフイン(以下(イ)と称す)と融点68〜70℃の
固形パラフイン(以下(ロ)と称す)を重量比で1:
1に混合するとこの混合したパラフイン(以下(ハ)
と称す)は、(イ)が溶剤のような作用をするためか
60℃でも液状の状態を保つている。即ち70℃以上
でしか使用出来なかつた(ロ)が(イ)と混合することに
より70℃以下でも使用可能になる。一方(イ)は56℃
以上で使用できるが、(ロ)に較べ分子量は低く、そ
の溶融粘度は低い。従つて溶融粘度が高いものが
必要な場合(ロ)を使用して70℃以上に加熱しなけれ
ばならない。
ところが(ハ)を使用すれば60℃以上でよく、しか
も(ハ)には分子量が(イ)より高くて溶融粘度を上げる
効果がある(ロ)が混合されており、(ロ)より低温で(イ)
より高粘度が達成できる。
又、(ハ)のような効果を上げようと仮りに融点が
60℃ぐらいの固形パラフイン(以下(ニ)と称す)を
もつて来ても、(ニ)は(ハ)に較べ分子量分布が狭く溶
融後のわずかな温度上昇で粘度低下が著しいため
(ハ)のようなすぐれた効果は示さないことは明白で
ある。仮りに融点をごく少し上まわる温度にすれ
ば可能な場合もあるかも知れないが、加熱装置の
温度制御幅を非常に狭くしなければならず事実上
不可能である。
以上述べたのはごく一例で二種以上の融点の異
なる潤滑剤をその融点、混合比率を選択すること
によつて所望の温度範囲で所望の溶融粘度が得ら
れる。
融点の異なる二種以上の有機潤滑剤を用いる場
合潤滑剤の加熱温度は最高の融点以下でかつ最低
の融点以上の温度であることが好ましい。加熱溶
融するために最低の融点以上の温度であることは
いうまでもないが、前述の如く溶融粘度を上げる
ために、又後述の如く加熱温度を下げることが好
ましいことから最高の融点以下の温度が好まし
い。本発明において、加熱溶融して塗布される潤
滑剤の塗布時の温度は潤滑剤の融点によつて決定
される。溶融した潤滑剤の溶融粘度を下げるため
には融点よりかなり高い温度が必要であり又、溶
融粘度を上げるためには融点より高温でしかも融
点に近い温度が必要とされる。加熱温度が150℃
を越えると、潤滑剤が分解し、更に煙を発生する
こともあるので150℃以下が好ましい。長時間加
熱を続けると潤滑剤が徐々に酸化変質して来るの
で120℃以下が更に好ましい範囲である。又、作
業時のやけど等安全面を考慮すれば100℃以下更
に好ましくは80℃以下が好適である。従つて潤滑
剤の好ましい融点範囲もこれによつて決定され
る。ここに述べたように、種々の制約で加熱溶融
温度が低い方が好ましく、先に述べた二種以上の
融点の異なる潤滑剤を混合して用いるのは、高融
点の潤滑剤がその融点以下で使用出来るので好ま
しい。潤滑剤の中で固形パラフインが最も好まし
いことは先に述べたが、種々の融点のものが揃つ
ていて加熱温度を低くしたい場合や、融点の異な
るものを混合する場合に選択の範囲が広くこれら
の意味も含めて好ましい潤滑剤といえる。
本発明において用いられるエナメル線には制限
はない。即ち丸線でも平角線でもよく、導体のサ
イズ、絶縁層の種類、構成、自己融着層の有無等
を問わない。あえていえば捲線されて使われるも
のであり、特に高速捲線されるものとか、手作業
でもすべりが要求される分野に使用されるもので
ある。又先に述べたように溶剤法と異なりクレー
ジングの心配がないのでどの品種にも適用でき
る。本発明において加熱溶融した潤滑剤を塗布す
る方法は、いかなる方法でも良い。勿論、均一に
塗布する方法が好ましいのはいうまでもない。
塗布する方法には、エナメル線を加熱溶融した
潤滑剤の中を直接通過させるデイツピング方式と
かミゾローラー方式、ワイパローラー方式等があ
る。又、フエルトに加熱溶融した潤滑剤をしみ込
ませこのフエルトの上又は間を通過させて塗布す
る方法もある。
フエルトは塗布と絞りを兼ねることも可能であ
る。勿論上記の塗布方法を組合せて行うこともで
きる。潤滑剤を塗布されたエナメル線はそのまま
使用することもできるし、又絞りを加えても良
い。絞りを行う理由は潤滑剤の塗布厚みを均一か
つ一定にするためである。絞りの方法は、いかな
る方法でもよい。例えばダイス絞り、ゴム絞り、
フエルト絞りがある。勿論、上記絞り方法を組合
せて使うこともできる。
潤滑剤は常温で固体であるため、エナメル線上
に塗布される時や塗布された後絞りを加えようと
する前に固化することがある。この時点で潤滑剤
が固化すると均一に塗布されなかつたり、絞りが
うまく出来ず、塗布厚みを一定にすることが出来
なくなる。
従つて、塗布部そして/又は絞り部を加熱する
ことが好ましい。
これにより潤滑剤の固化が防止出来るため、均
一な塗布や絞りが達成出来る。
塗布部そして/又は絞り部が加熱したフエルト
であることが一層好ましい。フエルト塗布そし
て/又は絞りはうすく、均一に塗布する方式とし
てすぐれており、このフエルトが加熱されている
と潤滑剤の固化が防止できるので好ましい。
フエルトを加熱する場合、フエルトは熱伝導が
悪いためあらかじめ溶融した潤滑剤をフエルトに
しみ込ませることも好ましい。こうしておいて、
フエルトに潤滑剤を供給すれば塗布と絞りが兼ね
て行える。別の方法で塗布を行い潤滑剤をしみ込
ませた加熱フエルトで絞る場合、仮りにエナメル
線上に塗布された潤滑剤が片面のみにしか付いて
いないような状態の時でも、全体に付きまわらせ
ることが出来る。塗布されたエナメル線自体をあ
らかじめ加熱しておくことも好ましい。エナメル
線が加熱されておれば、溶融した潤滑剤の固化を
防ぐことが出来るからである。
本発明においてエナメル線に塗布された潤滑剤
の塗布状態、厚み等については特に制限はない。
例えば、エナメル線上に不連続にもしくは片面の
みに潤滑剤が塗布されていても、捲線時にエナメ
ル線が損傷をうけるパスライン、ガイドローラー
等に、エナメル線に塗布された潤滑剤が付着し、
すべりが良くなり、損傷が軽減出きるからであ
る。しかしながら均一に塗布されていないという
ことは、滑りの悪い部分があるということで、損
傷をうける可能性は大きく、又、手作業で線を使
用するところでは、線のさばき、滑りが悪いので
均一に塗布されていることが好ましいのはいうま
でもない。
塗布厚みが厚いと、捲線機のパスライン、ガイ
ドローラー等に潤滑剤が付着し、機械を汚した
り、又かえつて滑り性を疎外することもあり、更
にむやみに潤滑剤が多いのは経済的でない。又多
すぎると線が粘着したり潤滑剤が剥離して落ちた
りすることもある。従つて均一にうすく塗布する
のが好ましい。このような理由でエナメル線上に
塗布される潤滑剤の平均の厚みが1ミクロン以下
であることが好ましい。
このようにして得られた潤滑性絶縁電線は潤滑
剤が塗布されていない未塗布のエナメル線に較
べ、すべり性が良くなつており、その目的は達成
される。
しかしながら、高速捲線機等で損傷なく、有効
に使用されるために、得られた潤滑性絶縁電線の
静摩擦係数は0.1以下が好ましい。
以下の実施例で本発明の内容を説明する。
尚、実施列の特性中、静摩擦係数は線間摩擦係
数で測定しその測定方法は、金属性ブロツクに平
行に2本のサンプル電線をとりつけ、これを平面
上におかれた平行な2本のサンプル電線の上に
各々の線が直角をなすようにおいて、前者の先に
荷重をのせ行うものである。
線さばき性は、電線をたばに取り、手触によつ
て線さばき、すべて性を見る官能試験によつた。
潤滑剤の厚みは、非常に薄く直接測定できない
ため、潤滑剤が塗布された電線を温水で加熱した
トルエン中に浸漬し、潤滑剤を洗い落して後、ト
ルエンを飛ばし、残つた潤滑剤の重量をはかりこ
れから厚みを計算した。
往復摩耗試験はJIS C3003の往復摩耗試験機を
用い荷重290gで行つた。
尚第1表中のオリジナルは潤滑剤を塗布してい
ないエナメル線である。
以下に実施例で使用た絶縁塗料を示す。
ワニスA:デラコートE 220G(日東電気工業
社より発売されているポリエステル絶縁塗料)
ワニスB:アイソミツドLV(日触スケネクタデ
イ社より発売されているポリエステルイミド絶
縁塗料)
ワニスC:HI−400(日立化成社より発売されて
いるポリアミドイミド絶縁塗料)
ワニスD:6.6−ナイロンをm−クレゾールに溶
解した絶縁塗料。
ワニスE:フエノキシ樹脂をm−クレゾールに溶
解した自己融着塗料。
実施例 1
直径0.65mmの銅線上にワニスAを数回繰返し塗
布焼付け、その上にワニスCを数回繰返し塗布焼
付け、更にその上に、融点54〜56℃の固形パラフ
イン400gと融点68〜70℃の固形パラフイン200g
を混合した固形パラフインを65℃で加熱溶融させ
塗布し、潤滑性絶縁電線を得た。固形パラフイン
は、ミゾローラーで塗布し、次いで塗布直後の電
線を、溶融したパラフインを浸み込ませたフエル
トで絞り更にゴムで絞つた。尚、フエルトは100
℃に加熱したブロツクをのせ、又ゴムはフエルト
に密接させておいた。得られた潤滑性絶縁電線の
特性を第1表に示す。
実施例 2
直径0.2mmの銅線上にワニスAを数回繰返し塗
布焼付け、その上にワニスDを塗布焼付け、更に
その上に融点54〜56℃の固形パラフイン400gと
融点68〜70℃の固形パラフイン200gを混合した
固形パラフインを70℃で加熱溶融させミゾローラ
ーで塗布し、更に溶融したパラフインを浸み込ま
せたフエルトで絞つて潤滑性絶縁電線を得た。
尚、フエルトには100℃に加熱したブロツクをの
せた。
得られた潤滑性絶縁電線の特性を第1表に示
す。
実施例 3
直径1.0mmの銅線上にワニスBを数回繰返し塗
布焼付け、その上にワニスCを数回繰返し塗布焼
付け、更にその上に融点54〜56℃の固形パラフイ
ン400gと融点68〜70℃の固形パラフインを混合
した固形パラフインを65℃で加熱溶融せしめミゾ
ローラーで塗布し、更に溶融パラフインを浸み込
ませたフエルトで絞つて潤滑性絶縁電線を得た。
尚、フエルトには100℃に加熱したブロツクをの
せた。
【表】DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a lubricious insulated wire with excellent windability. In recent years, electronics manufacturers that use enamelled wire have begun to use high-speed automatic wire winding machines in order to speed up the manufacturing process of devices.
However, in this case, although it appears that the processing cost of the equipment has been significantly reduced by speeding up the process, in reality, the enamelled wire is subjected to friction during winding, and the insulating layer is mechanically damaged. For this reason, after being incorporated into equipment, there is a serious problem in that rare shots occur and the loss rate increases significantly. In order to solve this problem, attempts have been made to impart lubricity to the enameled wire to reduce mechanical damage. This applies not only to automatic winding machines but also to manual winding. For example, when inserting enameled wire into a narrow slot in a motor, enamelled wire with good sliding properties is desired in order to improve the efficiency of manual winding. Since the enameled wire itself has poor lubricity, there is poor slippage between the enamelled wires, between the enameled wires and the winding machine, between the enameled wires and the equipment, and the insulating layer is damaged and work efficiency is reduced. For this reason, a method has been adopted in which a liquid lubricant such as liquid paraffin or refrigerating machine oil is applied onto the enameled wire. However, this method has the disadvantage of poor lubricity and slipperiness, resulting in poor wire handling by hand and poor alignment of transformers, coils, etc. during winding. The number of layered seats is increasing due to the expansion of the application of the inserter method that improves the space factor. Also, since this method uses a liquid lubricant, not only is it easy for dust to adhere to the wire, but it can also cause the wire to come loose after winding the coil, and have a negative impact on the adhesive strength of the adhesive tape used to secure the end. Another drawback is that the tape tends to peel off easily. In order to solve this problem, electrical manufacturers that wind coils sometimes use a method of passing the wire over lumps of solid paraffin and rubbing the solid paraffin onto the wire surface, but the amount of coating is uneven and is generally overused. There are drawbacks such as the electric wires quickly getting eaten into the solid paraffin, requiring replacement each time, and the need to repeat the process of melting, solidifying and regenerating frequently for regeneration, and reduced work efficiency. There is a strong demand for electric wire manufacturers to perform lubrication treatment according to the purpose and size, and to change the type and amount of lubricant depending on the purpose, size, etc. In response to this, electric wire manufacturers have no choice but to deal with the problem by dissolving approximately 1% solid paraffin in a solvent such as benzine or xylene and applying it to the wire surface, or heating and drying it after application. . However, in this method, since most of the solvent is solvent, a large amount of wasted solvent is consumed, exhaust equipment is required for hygiene and safety reasons, and equipment for removing the emitted solvent by combustion etc. is required as a pollution control measure. There is a risk of fire as it uses a solvent with a low flash point. Moreover, when performing heat drying, a heating furnace is required. Next, in terms of characteristics, when the solvent comes into contact with the wire surface, depending on the wire type, crazing occurs and the wire loses its commercial value, so the applicable types are limited, and the lubricant solution has a very low concentration. Because of the viscosity, it is not possible to control the thickness of the deposited film, so the only option is to allow the wire to adhere as it passes through the solution. Furthermore, solid paraffin has poor solubility in solvents, and there are major restrictions on the type and concentration of solvents.
Looking at solid organic lubricants other than solid paraffin, most of them are poorly soluble or insoluble in solvents, and even if they do dissolve, the concentration is low. Therefore, even if a desired solid organic lubricant is used, there are restrictions in that it cannot be used because it does not dissolve in the solvent, or even if it is dissolved, it can only be used at a low concentration. As mentioned above, the solution method has many disadvantages in terms of resource saving, pollution control, environmental health, and safety, and currently there are many restrictions in terms of the range of applicable properties and the range of applicable lubricants. However, the current situation is that we have no choice but to manufacture products while addressing contradictory points in order to meet the demands of consumers. The present inventors have arrived at the method of the present invention as a result of intensive studies to solve these problems. The present invention provides an insulated wire with excellent lubricity by heating and melting a solid organic lubricant at room temperature and applying it onto an enameled wire without using a solvent. In the present invention, since an organic lubricant that is solid at room temperature is used, it has better slipperiness than when using a liquid lubricant, and there is no adhesion of dust to the electric wire, and there is no adverse effect on the adhesive strength of the adhesive tape. Problems with liquid lubricants can be solved. In addition, in the present invention, an insulated wire with lubricity equivalent to or better than the solution method can be obtained, and since no solvent is used, no solvent is consumed and resources are saved, and there is no need for exhaust equipment for environmental health and safety.
There is no need for removal equipment such as combustion of discharged solvents as a pollution control measure, and there is no need to worry about fires caused by low flash point solvents.
Also, of course, a heating furnace for drying the solvent is not required. Furthermore, since there is no need to worry about crazing caused by solvents, there are no restrictions on the types of products to which it can be applied. Also, since it is a 100% lubricant, the thickness of the deposited film can be changed freely by controlling viscosity, temperature, amount of application, amount of squeezing, etc. Furthermore, since it is heated and melted, it has the advantage that lubricants that are poorly soluble or insoluble in solvents that cannot be used in the solution method can be used. The organic lubricant that is solid at room temperature used in the present invention may be any organic lubricant that melts when heated and that solidifies and exhibits lubricity after being applied to the enameled wire. Preferably, the lubricant is a compound having a long chain aliphatic group. This is because aliphatic groups have low polarity and good slipperiness. There are saturated and unsaturated aliphatic groups, but saturated is preferred because it has less polarity. The longer the alkyl group is, the more effective it can be, and it is particularly preferable that the alkyl group has 21 or more carbon atoms. It is preferable that the alkyl group has a straight chain shape as it has better slippage than a branched one. In particular, a part of the skeleton of the alkyl group consists of -( CH2- ) o , and n20 is preferable. The average molecular weight of the lubricant is preferably 100 or less. This is because if the molecular weight is too large, the melt viscosity will be high, making coating difficult, or the melting point or softening point will be too high, leading to thermal decomposition, which is undesirable. Next, examples of lubricants used in the present invention will be given. Among the various lubricants, those having the above-mentioned carbon number of the alkyl group, skeleton of the alkyl group,
Needless to say, it satisfies the average molecular weight, etc. Examples include hydrocarbons, fatty acids or derivatives thereof,
Examples include alcohol or its derivatives, fatty acid amide or its derivatives, waxes, greases, and the like. Of course, a mixture of these lubricants can also be used. More specific examples of lubricants are given below. It goes without saying that hydrocarbons with a large number of carbon atoms are preferred. There are saturated and unsaturated hydrocarbons, as well as linear and branched hydrocarbons, but the saturated and linear ones represented by the general formula CH 3 (CH 2 ) o CH 3 are preferable. Examples include heneicosane, docosane, tricosane, tetracosane, pentacosane, hexacosane, heptacosane, octacosane, nonacosane, triacontane, hentriacontane, dotriacontane, tritriacontane, tetratriacontane, pentatriacontane, hexatriacontane, heptatria Contane, octatriacontane, nonatriacontane, tetracontane, etc. Also preferred are hydrocarbons whose main component is saturated, straight-chain hydrocarbons, which are commercially available as so-called solid paraffin. Next, we will give examples of fatty acids or their derivatives. The fatty acid preferably has an alkyl group with a large number of carbon atoms, that is, a higher fatty acid. Higher fatty acids include saturated acids and unsaturated acids, and those with straight chain alkyl groups and those with branched alkyl groups. Also, depending on the number of functional groups, monocarboxylic acid, dicarboxylic acid,
Examples include tetracarboxylic acids. Among these, the general formula
Most preferred is a linear saturated monocarboxylic acid represented by CH 3 (CH 2 ) o COOH. The reason for this is that in order to exhibit a lubricating effect, it is better to have fewer polar groups. Examples of the most preferred linear saturated monocarboxylic acids among higher fatty acids include dodecanoic acid, tridecanoic acid, tetradecanoic acid, pentadecanoic acid, hexadecanoic acid, heptadecanoic acid, octadecanoic acid,
Nonadecanoic acid, eicosanoic acid, heneicosanoic acid, docosanoic acid, tricosanoic acid, tetracosanoic acid, pentacosanoic acid, hexacosanoic acid, heptacanoic acid, octacosanoic acid, nonacosanoic acid, triacontanoic acid, hentriacontanoic acid, dotriacontanoic acid, tetratriacontane acids, hexatriacontanoic acid, octatriacontanoic acid, etc. Acid anhydrides, esters, and fatty acid derivatives
There is salt, etc. Methyl alcohol for ester,
There are esters with various alcohols such as monohydric alcohols such as ethyl alcohol, dihydric alcohols such as ethylene glycol and diethylene glycol, trihydric alcohols such as glycerin and trimethylolpropane, and tetrahydric alcohols such as pentaerythritol. For imparting lubricity, it is preferable for the aliphatic group to be long, so esters with dihydric or higher alcohols are preferable. For the same reason, esters with higher alcohols are preferable to lower alcohols. Next, examples of alcohols or derivatives thereof will be shown. The alcohol is preferably one having an alkyl group with a large number of carbon atoms, that is, a higher alcohol. Higher alcohols include saturated alcohols and unsaturated alcohols, and those with straight-chain alkyl groups and those with branched alkyl groups. Furthermore, there are primary alcohols, secondary alcohols, and tertiary alcohols depending on the position of the functional group, and monohydric alcohols, dihydric alcohols, trihydric alcohols, etc. depending on the number of functional groups. Among these, the linear saturated primary monohydric alcohol represented by the general formula CH 3 (CH 2 ) o OH is most preferred for the reasons mentioned above. Examples include pentadecane 1-ol, hexadecane 1-ol
All, heptadecan 1-ol, octadecane 1-ol, nonadecan 1-ol, eicosan 1-ol, heneicosanol-1, docosanol-1, tetracosanol-1, pentacosanol-1, hexacosanol-1 , heptacosanol-1, octacosanol-1, nonacosanol-1, triacontanol-1, hentriacontanol-1, dotriacontanol-1, tritriacontanol-1, tetratriacontanol-1, pentatriacontanol-1 1, heptatriacontanol-1, etc. Examples of alcohol derivatives include esters with carboxylic acids, but particularly preferred are esters with the above-mentioned higher fatty acids. Next, examples of fatty acid amides or derivatives thereof will be given.
The fatty acid amide is preferably one having an alkyl group with a large number of carbon atoms, that is, a higher fatty acid amide. Hydrocarbon groups in the skeleton of fatty acid amide include those described above for fatty acids. Preferred among fatty acid amides are those represented by the general formula CH 3 (CH 2 ) o CONH 2 . Examples include palmitylamide, stearylamide, eicosylamide, docosylamide, hexacosylamide, octacosylamide, and the like. Derivatives of fatty acid amides include those with the hydrogen of the amino group replaced by an alkyl group, those with the general formula RCONH-CH 2 -NHCOR, RCONH
There is a bis fatty acid amide represented by -CH2 - CH2 -NHCOR. Examples of waxes include microcrystalline wax, carnauba wax, beeswax, and montan wax. Hoechstwax OP (chain length
C28-32 partially saponified ester wax from montanic acid), Hoechstwax E (ester wax from montanic acid), Hoechstwax S
(Montan acid wax) is also suitable. Among the lubricants mentioned above, solid paraffin is most preferred. Solid paraffin can be easily obtained at low cost, and since it is usually commercially available in different melting point ranges, one with a desired melting point can be selected. In addition, it is chemically stable, non-toxic, and suitable for handling. A feature of the present invention is that two or more organic lubricants having a melting point of 56°C or lower and an organic lubricant having a melting point of 60°C or higher are used as a mixture. When using a lubricant alone, the heating temperature must be higher than the melting point of the lubricant, but if a lubricant with a high melting point and a lubricant with a low melting point are used in combination, it can be melted at a temperature between the melting points of the two. Therefore, the heating temperature range is wide and the temperature control range of the heating device is wide.
Furthermore, the melt viscosity can be freely selected. This will be explained using solid paraffin as an example. Solid paraffin is generally commercially available in different melting point ranges, but using a mixture of paraffins with different melting points has the following advantages. For example, solid paraffin with a melting point of 54 to 56°C (hereinafter referred to as (a)) and solid paraffin with a melting point of 68 to 70°C (hereinafter referred to as (b)) are mixed in a weight ratio of 1:
When mixed with 1, this mixed paraffin (hereinafter (c)
) is because (a) acts like a solvent.
It remains liquid even at 60℃. That is, (b), which could only be used at temperatures above 70°C, can now be used at temperatures below 70°C by mixing it with (a). On the other hand (A) is 56℃
Although the above can be used, the molecular weight is lower than that of (b), and its melt viscosity is low. Therefore, if a material with a high melt viscosity is required, (b) must be used and heated to 70°C or higher. However, if (c) is used, the temperature is 60℃ or higher, and (b) is mixed with (b), which has a higher molecular weight than (b) and has the effect of increasing the melt viscosity, so it can be used at a lower temperature than (b). (stomach)
Higher viscosities can be achieved. Also, in order to increase the effect like (c), if the melting point is
Even if solid paraffin (hereinafter referred to as (d)) at about 60℃ is brought, (d) has a narrower molecular weight distribution than (c), and the viscosity decreases significantly with a slight temperature rise after melting.
It is clear that the excellent effect shown in (c) is not shown. It may be possible to do so if the temperature is slightly higher than the melting point, but this would require a very narrow temperature control range of the heating device, making it virtually impossible. The above-mentioned lubricants are just examples, and by selecting the melting points and mixing ratio of two or more lubricants having different melting points, a desired melt viscosity can be obtained in a desired temperature range. When two or more organic lubricants having different melting points are used, the heating temperature of the lubricants is preferably below the highest melting point and above the lowest melting point. Needless to say, the temperature is above the lowest melting point for heating and melting, but it is also below the highest melting point in order to increase the melt viscosity as described above, and because it is preferable to lower the heating temperature as described below. is preferred. In the present invention, the temperature at which the lubricant is applied by heating and melting is determined by the melting point of the lubricant. To lower the melt viscosity of a molten lubricant, a temperature considerably higher than the melting point is required, and to increase the melt viscosity, a temperature higher than the melting point but close to the melting point is required. Heating temperature is 150℃
If the temperature exceeds 150°C, the lubricant may decompose and even generate smoke, so a temperature of 150°C or lower is preferable. If heating is continued for a long time, the lubricant will gradually undergo oxidation and deterioration, so a temperature of 120°C or lower is more preferable. In addition, in consideration of safety such as burns during work, the temperature is preferably 100°C or lower, more preferably 80°C or lower. The preferred melting point range of the lubricant is therefore also determined by this. As mentioned here, due to various restrictions, it is preferable that the heating melting temperature is low, and when using a mixture of two or more lubricants with different melting points as mentioned above, it is recommended that the lubricant with a high melting point is lower than the melting point of the lubricant with a high melting point. This is preferable because it can be used in As mentioned earlier, solid paraffin is the most preferred among lubricants, but since it is available in various melting points, there is a wide range of choices when you want to lower the heating temperature or when mixing substances with different melting points. It can be said that it is a preferable lubricant considering these meanings. There are no restrictions on the enamelled wire used in the present invention. That is, the wire may be a round wire or a rectangular wire, and the size of the conductor, the type and structure of the insulating layer, the presence or absence of a self-bonding layer, etc. do not matter. To put it bluntly, it is used as a winding wire, especially in fields where high-speed winding is required, or where slippage is required even when manual work is performed. Also, as mentioned earlier, unlike the solvent method, there is no worry about crazing, so it can be applied to any variety. In the present invention, any method may be used to apply the heated and melted lubricant. Of course, it goes without saying that a method in which the coating is applied uniformly is preferable. Coating methods include a dipping method in which an enameled wire is directly passed through heated and molten lubricant, a groove roller method, and a wiper roller method. Alternatively, there is a method of impregnating heated and molten lubricant into felt and passing the lubricant over or between the felt to apply the lubricant. Felt can also be used for both coating and drawing. Of course, the above coating methods can also be combined. The enameled wire coated with lubricant can be used as is, or it can be squeezed. The reason for squeezing is to make the coating thickness of the lubricant uniform and constant. Any method may be used for the aperture. For example, die drawing, rubber drawing,
There is a felt diaphragm. Of course, the above aperture methods can also be used in combination. Since the lubricant is solid at room temperature, it may solidify when it is applied to the enamelled wire or before it is squeezed after being applied. If the lubricant solidifies at this point, it will not be applied uniformly or squeezed properly, making it impossible to maintain a constant coating thickness. Therefore, it is preferable to heat the application section and/or the squeezing section. This prevents the lubricant from solidifying, making it possible to achieve uniform application and squeezing. It is more preferable that the application part and/or the squeeze part be heated felt. Felt application and/or squeezing is an excellent method for applying thinly and uniformly, and heating the felt is preferred because it prevents solidification of the lubricant. When heating felt, it is also preferable to soak a molten lubricant into the felt in advance, since felt has poor thermal conductivity. In this way,
By supplying lubricant to the felt, it can be used for both application and squeezing. If the lubricant is applied using another method and squeezed using a heated felt soaked with lubricant, even if the lubricant applied to the enameled wire is only on one side, it should be applied to the entire wire. I can do it. It is also preferable to heat the coated enameled wire itself in advance. This is because if the enameled wire is heated, it is possible to prevent the molten lubricant from solidifying. In the present invention, there are no particular limitations on the coating state, thickness, etc. of the lubricant applied to the enameled wire.
For example, even if lubricant is applied discontinuously or only on one side of the enameled wire, the lubricant applied to the enamelled wire will adhere to pass lines, guide rollers, etc. where the enameled wire is damaged during winding.
This is because it improves slippage and reduces damage. However, the fact that it is not applied evenly means that there are areas with poor slippage, which increases the possibility of damage.Also, in places where the wire is used by hand, the line is not well distributed and slippery, so it is not evenly coated. Needless to say, it is preferable that the coating be applied to If the coating thickness is too thick, the lubricant will adhere to the pass lines, guide rollers, etc. of the winding machine, contaminating the machine or even impairing the slipperiness. Furthermore, it is not economical to use too much lubricant. Not. Also, if there is too much, the wire may become sticky or the lubricant may peel off and fall off. Therefore, it is preferable to apply it evenly and thinly. For this reason, it is preferable that the average thickness of the lubricant applied to the enameled wire is 1 micron or less. The lubricated insulated wire thus obtained has better sliding properties than an uncoated enamelled wire that is not coated with a lubricant, thus achieving the objective. However, in order to be effectively used without damage in a high-speed winding machine or the like, the coefficient of static friction of the obtained lubricant insulated wire is preferably 0.1 or less. The following examples illustrate the invention. In addition, among the characteristics of the actual series, the static friction coefficient is measured by the line-to-line friction coefficient, and the measurement method is to attach two sample electric wires in parallel to a metal block, and then connect them to two parallel wires placed on a flat surface. Each wire is placed at right angles to the sample electric wire, and a load is placed on the tip of the former. Wire handling properties were determined through a sensory test in which a wire was picked up from a cigarette and the wire was handled to the touch to determine the quality. The thickness of the lubricant is too thin to measure directly, so the lubricant-coated wire is immersed in toluene heated with hot water, the lubricant is washed off, the toluene is blown off, and the weight of the remaining lubricant is measured. The thickness was calculated from this. The reciprocating abrasion test was conducted using a JIS C3003 reciprocating abrasion tester with a load of 290 g. Note that the original in Table 1 is an enameled wire without lubricant applied thereto. The insulating paints used in the examples are shown below. Varnish A: Delacote E 220G (polyester insulating paint sold by Nitto Electric Industries, Ltd.) Varnish B: Isomyd LV (polyester imide insulating paint sold by Nippon Schenectaday Co., Ltd.) Varnish C: HI-400 (Hitachi Chemical Co., Ltd.) Varnish D: An insulating paint made by dissolving 6.6-nylon in m-cresol. Varnish E: Self-fusing paint made by dissolving phenoxy resin in m-cresol. Example 1 Varnish A was repeatedly coated and baked on a copper wire with a diameter of 0.65 mm several times. Varnish C was repeatedly coated and baked on top of that several times, and then 400 g of solid paraffin with a melting point of 54-56°C and a melting point of 68-70 200g solid paraffin at ℃
A lubricious insulated wire was obtained by heating and melting a solid paraffin mixture at 65°C. The solid paraffin was applied with a groove roller, and then the electric wire immediately after the application was squeezed with a felt impregnated with molten paraffin, and further squeezed with a rubber. In addition, felt is 100
A block heated to ℃ was placed on it, and the rubber was kept in close contact with the felt. Table 1 shows the properties of the obtained lubricious insulated wire. Example 2 Varnish A was repeatedly coated and baked on a copper wire with a diameter of 0.2 mm several times. Varnish D was coated and baked on top of that, and then 400 g of solid paraffin with a melting point of 54 to 56°C and solid paraffin with a melting point of 68 to 70°C were added on top of that. A lubricious insulated wire was obtained by heating and melting 200 g of solid paraffin mixed at 70°C, applying it with a groove roller, and squeezing it with felt impregnated with the melted paraffin.
A block heated to 100°C was placed on the felt. Table 1 shows the properties of the obtained lubricious insulated wire. Example 3 Varnish B was repeatedly coated and baked several times on a copper wire with a diameter of 1.0 mm. Varnish C was repeatedly coated and baked on top of that several times, and then 400 g of solid paraffin with a melting point of 54 to 56°C and a melting point of 68 to 70°C were added on top of that. Solid paraffin mixed with solid paraffin was heated and melted at 65°C, applied with a groove roller, and further squeezed with felt impregnated with molten paraffin to obtain a lubricating insulated wire.
A block heated to 100°C was placed on the felt. 【table】
Claims (1)
メル線上に塗布する方法において、融点が56℃以
下の有機潤滑剤と融点が60℃以上の有機潤滑剤と
を二種以上混合して用いることを特徴とする潤滑
性絶縁電線の製造方法。 2 二種以上の有機潤滑剤の最高の融点以下で、
かつ最低の融点以上の温度で有機潤滑剤を加熱溶
融する特許請求の範囲第1項記載の潤滑性絶縁電
線の製造方法。 3 潤滑性絶縁電線の静摩擦係数が0.1以下であ
る特許請求の範囲第1項記載の潤滑性絶縁電線の
製造方法。 4 二種以上の常温で固体の有機潤滑剤の少くと
も一つの有機潤滑剤のアルキル基の炭素数が21以
上のものを主成分とする特許請求の範囲第1項記
載の潤滑性絶縁電線の製造方法。 5 アルキル基の骨格の一部が−(CH2−)oから成
り、n20である特許請求の範囲第4項記載の潤
滑性絶縁電線の製造方法。 6 潤滑剤の平均分子量が1000以下である特許請
求の範囲第1項記載の潤滑性絶縁電線の製造方
法。 7 エナメル線上に塗布される潤滑剤の平均の厚
みが1ミクロン以下である特許請求の範囲第1項
記載の潤滑性絶縁電線の製造方法。[Claims] 1. A method of heating and melting an organic lubricant that is solid at room temperature and applying it to an enameled wire, which comprises two types of organic lubricants: one with a melting point of 56°C or lower and one with a melting point of 60°C or higher. A method for manufacturing a lubricating insulated wire, characterized by using a mixture of the above. 2 below the highest melting point of two or more organic lubricants,
2. The method for producing a lubricating insulated wire according to claim 1, wherein the organic lubricant is heated and melted at a temperature equal to or higher than the lowest melting point. 3. The method for manufacturing a lubricious insulated wire according to claim 1, wherein the lubricious insulated wire has a static friction coefficient of 0.1 or less. 4. A lubricious insulated wire according to claim 1, wherein the main component is at least one organic lubricant having an alkyl group of 21 or more carbon atoms among two or more organic lubricants that are solid at room temperature. Production method. 5. The method for producing a lubricious insulated wire according to claim 4, wherein a part of the skeleton of the alkyl group consists of -( CH2- ) o and is n20. 6. The method for producing a lubricating insulated wire according to claim 1, wherein the lubricant has an average molecular weight of 1000 or less. 7. The method for producing a lubricating insulated wire according to claim 1, wherein the average thickness of the lubricant applied to the enameled wire is 1 micron or less.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16302378A JPS5588211A (en) | 1978-12-26 | 1978-12-26 | Method of fabricating lubricated insulated wire |
| CH1147079A CH640972A5 (en) | 1978-12-26 | 1979-12-27 | Method for producing a lubricated, insulated wire |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16302378A JPS5588211A (en) | 1978-12-26 | 1978-12-26 | Method of fabricating lubricated insulated wire |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5588211A JPS5588211A (en) | 1980-07-03 |
| JPS623527B2 true JPS623527B2 (en) | 1987-01-26 |
Family
ID=15765707
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16302378A Granted JPS5588211A (en) | 1978-12-26 | 1978-12-26 | Method of fabricating lubricated insulated wire |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JPS5588211A (en) |
| CH (1) | CH640972A5 (en) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5762315U (en) * | 1980-09-30 | 1982-04-13 | ||
| US4350738A (en) * | 1981-10-13 | 1982-09-21 | Essex Group, Inc. | Power insertable polyamide-imide coated magnet wire |
| US4385435A (en) * | 1981-10-13 | 1983-05-31 | United Technologies Corporation | Method of power inserting polyamide-imide coated magnet wire |
| US4406055A (en) * | 1981-10-19 | 1983-09-27 | Essex Group, Inc. | Power insertable polyamide-imide coated magnet wire |
| US4385437A (en) * | 1981-10-19 | 1983-05-31 | United Technologies Corporation | Method of power inserting polyamide-imide coated magnet wire |
| US4390590A (en) * | 1981-10-19 | 1983-06-28 | Essex Group, Inc. | Power insertable polyamide-imide coated magnet wire |
| US4348460A (en) * | 1981-10-19 | 1982-09-07 | Essex Group, Inc. | Power insertable polyamide-imide coated magnet wire |
| JPS62154408A (en) * | 1985-12-25 | 1987-07-09 | 住友電気工業株式会社 | Lubricative insulated wire |
| JPS62154409A (en) * | 1985-12-25 | 1987-07-09 | 住友電気工業株式会社 | Lubricative insulated wire |
| JPS62200605A (en) * | 1986-02-27 | 1987-09-04 | 古河電気工業株式会社 | Processing resistant insulated wire |
| CN101527193B (en) * | 2009-04-24 | 2012-07-04 | 浙江长城电工科技股份有限公司 | Method for coating surface lubricant on lacquered wire and coating device thereof |
| CN103219099A (en) * | 2013-03-29 | 2013-07-24 | 诚信漆包线(惠州)有限公司 | Environmental-friendly type varnished wire lubricating oil coating device |
| CN103247393A (en) * | 2013-05-22 | 2013-08-14 | 江苏句容联合铜材有限公司 | Paper-covered wire anti-damage device |
| CN103928197B (en) * | 2014-04-23 | 2016-06-29 | 湖州三行线缆有限公司 | Roller shaft type surface lubricant coating device for enamelled wires and application thereof |
| CN103909045B (en) * | 2014-04-23 | 2016-07-06 | 湖州三行线缆有限公司 | Enamelled wire surface lubricant painting method and coating unit and application thereof |
| CN105220550B (en) * | 2015-10-23 | 2018-05-25 | 苏州市吴江神州双金属线缆有限公司 | A kind of oiling station in the production for cable |
| EP3389059A1 (en) * | 2017-04-10 | 2018-10-17 | Siemens Aktiengesellschaft | Winding wire and use of same |
| CN111554455B (en) * | 2020-06-10 | 2024-12-06 | 无锡统力电工有限公司 | A device for coating solid paraffin on the surface of a wrapped conductor |
| CN114220653A (en) * | 2021-12-08 | 2022-03-22 | 深圳麦格米特电气股份有限公司 | Enameled stranded wire preparation method, enameled stranded wire and transformer |
-
1978
- 1978-12-26 JP JP16302378A patent/JPS5588211A/en active Granted
-
1979
- 1979-12-27 CH CH1147079A patent/CH640972A5/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5588211A (en) | 1980-07-03 |
| CH640972A5 (en) | 1984-01-31 |
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