JPH0824015B2 - Method for manufacturing foam insulated wire - Google Patents
Method for manufacturing foam insulated wireInfo
- Publication number
- JPH0824015B2 JPH0824015B2 JP62053700A JP5370087A JPH0824015B2 JP H0824015 B2 JPH0824015 B2 JP H0824015B2 JP 62053700 A JP62053700 A JP 62053700A JP 5370087 A JP5370087 A JP 5370087A JP H0824015 B2 JPH0824015 B2 JP H0824015B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- acid
- insulated wire
- azodicarbonamide
- 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 - Fee Related
Links
- 239000006260 foam Substances 0.000 title claims description 20
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 238000000034 method Methods 0.000 title description 5
- 239000004156 Azodicarbonamide Substances 0.000 claims description 22
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 claims description 22
- 235000019399 azodicarbonamide Nutrition 0.000 claims description 22
- 239000004020 conductor Substances 0.000 claims description 20
- 239000012212 insulator Substances 0.000 claims description 17
- 238000000354 decomposition reaction Methods 0.000 claims description 15
- 229920000098 polyolefin Polymers 0.000 claims description 10
- 239000011701 zinc Substances 0.000 claims description 9
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 7
- 239000000344 soap Substances 0.000 claims description 7
- 229910052725 zinc Inorganic materials 0.000 claims description 7
- 238000001125 extrusion Methods 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 230000005865 ionizing radiation Effects 0.000 claims description 3
- 239000011342 resin composition Substances 0.000 claims description 3
- 238000005187 foaming Methods 0.000 description 15
- 239000002253 acid Substances 0.000 description 13
- 229920001684 low density polyethylene Polymers 0.000 description 10
- 239000004702 low-density polyethylene Substances 0.000 description 10
- 238000009413 insulation Methods 0.000 description 8
- 239000004088 foaming agent Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 238000010894 electron beam technology Methods 0.000 description 3
- 238000007765 extrusion coating Methods 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 3
- BITHHVVYSMSWAG-KTKRTIGZSA-N (11Z)-icos-11-enoic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCC(O)=O BITHHVVYSMSWAG-KTKRTIGZSA-N 0.000 description 2
- YWWVWXASSLXJHU-AATRIKPKSA-N (9E)-tetradecenoic acid Chemical compound CCCC\C=C\CCCCCCCC(O)=O YWWVWXASSLXJHU-AATRIKPKSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- CNVZJPUDSLNTQU-SEYXRHQNSA-N petroselinic acid Chemical compound CCCCCCCCCCC\C=C/CCCCC(O)=O CNVZJPUDSLNTQU-SEYXRHQNSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- -1 polypropylene Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003751 zinc Chemical class 0.000 description 2
- GAWWVVGZMLGEIW-GNNYBVKZSA-L zinc ricinoleate Chemical compound [Zn+2].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O.CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O GAWWVVGZMLGEIW-GNNYBVKZSA-L 0.000 description 2
- 229940100530 zinc ricinoleate Drugs 0.000 description 2
- YHGJECVSSKXFCJ-KUBAVDMBSA-N (6Z,9Z,12Z,15Z,18Z,21Z)-tetracosahexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCCC(O)=O YHGJECVSSKXFCJ-KUBAVDMBSA-N 0.000 description 1
- CUXYLFPMQMFGPL-UHFFFAOYSA-N (9Z,11E,13E)-9,11,13-Octadecatrienoic acid Natural products CCCCC=CC=CC=CCCCCCCCC(O)=O CUXYLFPMQMFGPL-UHFFFAOYSA-N 0.000 description 1
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- GCORITRBZMICMI-CMDGGOBGSA-N (e)-dodec-4-enoic acid Chemical compound CCCCCCC\C=C\CCC(O)=O GCORITRBZMICMI-CMDGGOBGSA-N 0.000 description 1
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 1
- OXEDXHIBHVMDST-UHFFFAOYSA-N 12Z-octadecenoic acid Natural products CCCCCC=CCCCCCCCCCCC(O)=O OXEDXHIBHVMDST-UHFFFAOYSA-N 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- KIHBGTRZFAVZRV-UHFFFAOYSA-N 2-Hydroxyoctadecanoic acid Natural products CCCCCCCCCCCCCCCCC(O)C(O)=O KIHBGTRZFAVZRV-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- YWWVWXASSLXJHU-UHFFFAOYSA-N 9E-tetradecenoic acid Natural products CCCCC=CCCCCCCCC(O)=O YWWVWXASSLXJHU-UHFFFAOYSA-N 0.000 description 1
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- GCORITRBZMICMI-UHFFFAOYSA-N Linderic acid Natural products CCCCCCCC=CCCC(O)=O GCORITRBZMICMI-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- CNVZJPUDSLNTQU-UHFFFAOYSA-N Petroselaidic acid Natural products CCCCCCCCCCCC=CCCCCC(O)=O CNVZJPUDSLNTQU-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241001125046 Sardina pilchardus Species 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- CUXYLFPMQMFGPL-SUTYWZMXSA-N all-trans-octadeca-9,11,13-trienoic acid Chemical compound CCCC\C=C\C=C\C=C\CCCCCCCC(O)=O CUXYLFPMQMFGPL-SUTYWZMXSA-N 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229940114079 arachidonic acid Drugs 0.000 description 1
- 235000021342 arachidonic acid Nutrition 0.000 description 1
- 125000005603 azodicarboxylic group Chemical group 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229940108623 eicosenoic acid Drugs 0.000 description 1
- BITHHVVYSMSWAG-UHFFFAOYSA-N eicosenoic acid Natural products CCCCCCCCC=CCCCCCCCCCC(O)=O BITHHVVYSMSWAG-UHFFFAOYSA-N 0.000 description 1
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
- 235000021299 gondoic acid Nutrition 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- OYHQOLUKZRVURQ-AVQMFFATSA-N linoelaidic acid Chemical compound CCCCC\C=C\C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-AVQMFFATSA-N 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 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
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 235000019512 sardine Nutrition 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- AQWHMKSIVLSRNY-UHFFFAOYSA-N trans-Octadec-5-ensaeure Natural products CCCCCCCCCCCCC=CCCCC(O)=O AQWHMKSIVLSRNY-UHFFFAOYSA-N 0.000 description 1
- MEYZYGMYMLNUHJ-UHFFFAOYSA-N tunicamycin Natural products CC(C)CCCCCCCCCC=CC(=O)NC1C(O)C(O)C(CC(O)C2OC(C(O)C2O)N3C=CC(=O)NC3=O)OC1OC4OC(CO)C(O)C(O)C4NC(=O)C MEYZYGMYMLNUHJ-UHFFFAOYSA-N 0.000 description 1
- 229920001862 ultra low molecular weight polyethylene Polymers 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
- 229940098697 zinc laurate Drugs 0.000 description 1
- NPJHXSZKSBSLLK-UHFFFAOYSA-L zinc;2-hydroxyoctadecanoate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCC(O)C([O-])=O.CCCCCCCCCCCCCCCCC(O)C([O-])=O NPJHXSZKSBSLLK-UHFFFAOYSA-L 0.000 description 1
- GPYYEEJOMCKTPR-UHFFFAOYSA-L zinc;dodecanoate Chemical compound [Zn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O GPYYEEJOMCKTPR-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Processes Specially Adapted For Manufacturing Cables (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は、高発泡化が可能であり、しかも導体と発泡
絶縁体との粘着を防止した発泡絶縁電線の製造方法に関
するものである。TECHNICAL FIELD The present invention relates to a method for producing a foam-insulated electric wire, which is capable of high foaming and which prevents adhesion between a conductor and a foam insulator.
[従来の技術] コンピュータ、電話通信などの高速情報回路において
は、低誘電率の電線が必要とされており、発泡ポリオレ
フィン絶縁電線が多用されてきている。発泡ポリオレフ
ィン絶縁電線の製造方法としては、化学発泡剤を含むポ
リオレフィンを押出機に供給して発泡剤の分解温度以上
の温度でもって溶融混練し、導体外周に押出被覆する方
法が一般に知られているが、この方法では、発泡剤の分
解ガスが飛散しやすく、50%以上の高発泡体を得ること
が困難な状況にある。[Background Art] In high-speed information circuits such as computers and telephone communications, low dielectric constant electric wires are required, and foamed polyolefin insulated electric wires are frequently used. As a method for producing a foamed polyolefin insulated wire, a method is generally known in which a polyolefin containing a chemical foaming agent is supplied to an extruder, melt-kneaded at a temperature equal to or higher than the decomposition temperature of the foaming agent, and extruded around the conductor. However, in this method, the decomposition gas of the foaming agent is liable to be scattered, and it is difficult to obtain a high foam of 50% or more.
発泡剤の分解ガスの飛散を防止する対策として、特公
昭53−4909には、発泡剤を含むプラスチック混和物を導
体上に押出被覆した後、放射線、電子線により連続的に
架橋し、続いて加圧流体雰囲気中で加熱して発泡させる
製造方法が提案されている。As a measure to prevent the decomposition gas of the foaming agent from scattering, in JP-B-53-4909, a plastic mixture containing a foaming agent is extrusion-coated on a conductor and then continuously crosslinked by radiation and electron beams, There has been proposed a manufacturing method in which foaming is performed by heating in a pressurized fluid atmosphere.
[発明が解決しようとする問題点] しかし、この方法によれば、流体加圧設備が必要であ
ることから汎用性に欠け、また、圧力変動による外径の
不均一、流体による絶縁電線の汚損などの問題がある。[Problems to be Solved by the Invention] However, this method lacks versatility due to the necessity of a fluid pressurizing facility, and has non-uniform outer diameter due to pressure fluctuation, and contamination of insulated wires due to fluid. There is such a problem.
このため、常圧下での加熱発泡について種々検討した
ところ、発泡剤として最も適切なアゾジカルボンアミド
を使用した場合、導体と発泡絶縁体とが粘着し、ワイヤ
ストリッパを用いて発泡絶縁体を剥取る際、導体周囲に
発泡絶縁体が残り、端末処理作業性が極めて悪くなるこ
とが指摘されるに至った。For this reason, various studies were conducted on heat foaming under normal pressure. When the most suitable azodicarbonamide was used as a foaming agent, the conductor and foamed insulation adhered and the foamed insulation was peeled off using a wire stripper. At this time, it has been pointed out that the foam insulation remains around the conductor and the workability of the terminal treatment is extremely deteriorated.
本発明は、上記に基づいてなされたもので、高発泡化
が可能であり、しかも導体と発泡絶縁体との粘着を抑制
して発泡絶縁体の剥離を容易とする発泡絶縁電線の製造
方法の提供を目的とするものである。The present invention has been made on the basis of the above, and is a method for manufacturing a foam insulated wire, which is capable of high foaming, and which suppresses adhesion between a conductor and a foam insulating material and facilitates peeling of the foam insulating material. It is intended to be provided.
[問題点を解決するための手段] 本発明の発泡絶縁電線の製造方法は、ポリオレフィン
100重量部に対してアゾジカルボンアミド0.5〜15重量部
および式Zn(OOCR)2で示される亜鉛石鹸(Rは炭素数
7以上のアルキル基)0.05〜5重量部含有する樹脂組成
物をアゾジカルボンアミドの分解温度以下の温度で導体
外周に押出被覆してから電離性放射線の照射により架橋
せしめ、しかる後アゾジカルボンアミドの分解温度以上
に加熱して発泡絶縁体を形成することを特徴とするもの
である。[Means for Solving the Problems] The method for producing a foamed insulated wire according to the present invention comprises a polyolefin
Azodicarboxylic resin composition containing 0.5 to 15 parts by weight of azodicarbonamide and 0.05 to 5 parts by weight of zinc soap (R is an alkyl group having 7 or more carbon atoms) represented by the formula Zn (OOCR) 2 with respect to 100 parts by weight. Characterized by extrusion coating the outer circumference of a conductor at a temperature not higher than the decomposition temperature of amide and then crosslinking by irradiation with ionizing radiation, and then heating to a temperature not lower than the decomposition temperature of azodicarbonamide to form a foamed insulator. Is.
本発明におえるポリオレフィンとしては、低密度ポリ
エチレン、中高密度ポリエチレン、リニア低密度ポリエ
チレン、超低密度ポリエチレン、ポリプロピレンなどが
例示されるが、これに限るものではない。Examples of the polyolefin in the present invention include, but are not limited to, low density polyethylene, medium and high density polyethylene, linear low density polyethylene, ultra low density polyethylene, polypropylene and the like.
アゾジカルボンアミドは、分解温度が200〜210℃の粉
末物質であり、分解によって発生するガスにより、発泡
体が形成される。アゾジカルボンアミドの添加量は、ポ
リオレフィン100重量部に対して0.5〜15重量部の範囲と
する必要があり、0.5重量部未満では発泡が不十分であ
り、15重量部を越えると発泡状態のコントロールが難し
くなる。Azodicarbonamide is a powder substance having a decomposition temperature of 200 to 210 ° C., and a gas generated by the decomposition forms a foam. The addition amount of azodicarbonamide must be in the range of 0.5 to 15 parts by weight per 100 parts by weight of polyolefin, and if it is less than 0.5 part by weight, foaming is insufficient, and if it exceeds 15 parts by weight, the foaming state is controlled. Becomes difficult.
式Zn(OOCR)2で示される亜鉛石鹸(Rは炭素数7以
上のアルキル基)は、導体と発泡絶縁体との粘着を抑制
するために添加するものである。すなわち、導体と発泡
絶縁体との粘着は、アゾジカルボンアミドの分解残渣に
よるものであり、亜鉛石鹸はこの分解残渣が生成される
のを抑制するものである。亜鉛石鹸の添加量は、ポリオ
レフィン100重量部に対して0.05〜5重量部の範囲であ
り、0.05重量部未満では導体と発泡絶縁体との粘着防止
に効果がなく、5重量部を越えるとアゾジカルボンアミ
ドの分解温度を著しく低下させるため、押出成形時に発
泡してしまうことになる。The zinc soap represented by the formula Zn (OOCR) 2 (R is an alkyl group having 7 or more carbon atoms) is added to suppress the adhesion between the conductor and the foamed insulator. That is, the adhesion between the conductor and the foamed insulator is due to the decomposition residue of azodicarbonamide, and the zinc soap suppresses the generation of this decomposition residue. The amount of zinc soap added is in the range of 0.05 to 5 parts by weight with respect to 100 parts by weight of the polyolefin. Since the decomposition temperature of dicarbonamide is remarkably lowered, foaming occurs during extrusion molding.
亜鉛石鹸としては、ステアリン酸、ラウリン酸、リシ
ノール酸、ナフテン酸、2−エチルヘキソイン酸、オク
チル酸、ヒドロキシステアリン酸、フタル酸などの亜鉛
塩が好適であるが、さらに、リンデル酸、エライジン
酸、ツズ酸、カドレン酸、フィセトレイン酸、ゴンドウ
酸、ミリストレイン酸、鯨油酸、ゾーマリン酸、エルカ
酸、ペトロセリン酸、プランジン酸、オレイン酸、セラ
コイレン酸、リノール酸、リノエライジン酸、リノレン
酸、エレオステアリン酸、モロクチ酸、バリナリン酸、
アラキドン酸、イワシ酸、ヒラガシラ酸、ニシン酸など
の亜鉛塩が例示される。As the zinc soap, zinc salts such as stearic acid, lauric acid, ricinoleic acid, naphthenic acid, 2-ethylhexoic acid, octylic acid, hydroxystearic acid, and phthalic acid are preferable, and further, linderic acid, elaidic acid, and tunic acid. Duzic acid, cadrenic acid, ficetrain acid, gondoic acid, myristoleic acid, whale oil acid, zomarinic acid, erucic acid, petroselinic acid, prandic acid, oleic acid, ceracoilenic acid, linoleic acid, linoelaidic acid, linolenic acid, eleo Stearic acid, moloctic acid, valinaric acid,
Examples include zinc salts such as arachidonic acid, sardine acid, hiragashicholic acid and nisinic acid.
ポリオレフィン、アゾジカルボンアミドおよび亜鉛石
鹸を必須成分として含有する樹脂組成物は、アゾジカル
ボンアミドの分解温度以下の温度、例えば160℃以下の
温度で溶融混練を行い、導体外周に押出被覆する。続い
て、電子線などの電離性放射線を0.5〜5Mradの範囲で照
射して架橋し、常圧下でアゾジカルボンアミドの分解温
度以上に加熱して発泡絶縁体を形成する。この加熱は、
電気炉などを用いて連続的に行うのが好ましく、設定温
度は、アゾジカルボンアミドの分解温度よりも数十度高
くすることが好ましい。当然ではあるが、ポリオレフィ
ンが分解してしまうような高温は避けるべきである。The resin composition containing polyolefin, azodicarbonamide and zinc soap as essential components is melt-kneaded at a temperature not higher than the decomposition temperature of azodicarbonamide, for example at a temperature not higher than 160 ° C., and extrusion-coated on the outer circumference of the conductor. Subsequently, ionizing radiation such as an electron beam is irradiated in the range of 0.5 to 5 Mrad to crosslink, and the foamed insulator is formed by heating at a temperature not lower than the decomposition temperature of azodicarbonamide under normal pressure. This heating
It is preferable to carry out continuously using an electric furnace or the like, and the set temperature is preferably higher than the decomposition temperature of azodicarbonamide by several tens of degrees. Of course, high temperatures at which the polyolefin decomposes should be avoided.
[発明の実施例] 実施例1 低密度ポリエチレン(宇部興産UBEC−400)100重量部
にアゾジカルボンアミド3重量部を添加し、これを135
℃に設定した8インチロールで混練してからステアリン
酸亜鉛0.5重量部添加してコンパウンドとした。このコ
ンパウンドを28mm押出機(設定温度130℃)に導入して
溶融混練を行い、外径0.45mmのスズメッキ銅線外周に厚
さ1.0mmに押出被覆してした。続いて、電子線照射装置
により1.5Mrad照射して架橋を行い、300℃に設定した内
径70mmφ、炉長2.5mの筒型電気炉中を常圧下で通過させ
ることにより発泡絶縁電線を製造した。[Examples of the Invention] Example 1 To 100 parts by weight of low-density polyethylene (UBEC-400 manufactured by Ube Industries, Ltd.), 3 parts by weight of azodicarbonamide was added, and 135 parts of this was added.
The mixture was kneaded with an 8-inch roll set at 0 ° C., and then 0.5 part by weight of zinc stearate was added to obtain a compound. This compound was introduced into a 28 mm extruder (set temperature 130 ° C.), melt-kneaded, and extrusion-coated to a thickness of 1.0 mm on the outer circumference of a tin-plated copper wire having an outer diameter of 0.45 mm. Subsequently, 1.5 Mrad was irradiated by an electron beam irradiation device to perform cross-linking, and the foamed insulated wire was manufactured by passing through a cylindrical electric furnace having an inner diameter of 70 mmφ and a furnace length of 2.5 m set at 300 ° C. under normal pressure.
この絶縁電線の発泡度は約68%であり、しかも、発泡
絶縁体のワイヤストリッパによる剥取りは極めて容易で
あった。The degree of foaming of this insulated wire was about 68%, and the foamed insulator was extremely easily peeled off by the wire stripper.
実施例2 低密度ポリエチレン(宇部興産UBEC−400)100重量部
にアゾジカルボンアミド3重量部およびリシノール酸亜
鉛0.5重量部を添加した以外は実施例1と同様にして発
泡絶縁電線を製造した。Example 2 A foam insulated wire was produced in the same manner as in Example 1 except that 3 parts by weight of azodicarbonamide and 0.5 part by weight of zinc ricinoleate were added to 100 parts by weight of low-density polyethylene (UBEC-400 manufactured by Ube Industries).
この絶縁電線の発泡度は約71%であり、しかも、発泡
絶縁体のワイヤストリッパによる剥取りは極めて容易で
あった。The degree of foaming of this insulated wire was about 71%, and it was extremely easy to peel off the foamed insulation with a wire stripper.
実施例3 低密度ポリエチレン(三井石油化学ミラソン3530)10
0重量部にアゾジカルボンアミド4重量部およびステア
リン酸亜鉛0.3重量部を添加した以外は実施例1と同様
にして発泡絶縁電線を製造した。Example 3 Low-density polyethylene (Mitsui Petrochemical Mirason 3530) 10
A foam insulated wire was produced in the same manner as in Example 1 except that 4 parts by weight of azodicarbonamide and 0.3 part by weight of zinc stearate were added to 0 parts by weight.
この絶縁電線の発泡度は約73%であり、しかも、発泡
絶縁体のワイヤストリッパによる剥取りは極めて容易で
あった。The degree of foaming of this insulated wire was about 73%, and it was extremely easy to peel off the foamed insulation with a wire stripper.
実施例4 低密度ポリエチレン(三井石油化学ミラソン3530)10
0重量部にアゾジカルボンアミド4重量部およびラウリ
ン酸亜鉛0.7重量部を添加した以外は実施例1と同様に
して発泡絶縁電線を製造した。Example 4 Low-density polyethylene (Mitsui Petrochemical Mirason 3530) 10
A foam insulated wire was produced in the same manner as in Example 1 except that 4 parts by weight of azodicarbonamide and 0.7 parts by weight of zinc laurate were added to 0 parts by weight.
この絶縁電線の発泡度は約74%であり、しかも、発泡
絶縁体のワイヤストリッパによる剥取りは極めて容易で
あった。The foamed degree of this insulated wire was about 74%, and the foamed insulator was extremely easily peeled off by the wire stripper.
実施例5 低密度ポリエチレン(三井石油化学ミラソン3530)10
0重量部にアゾジカルボンアミド4重量部およびナフテ
ン酸亜鉛0.5重量部を添加した以外は実施例1と同様に
して発泡絶縁電線を製造した。Example 5 Low-density polyethylene (Mitsui Petrochemical Mirason 3530) 10
A foam insulated wire was produced in the same manner as in Example 1 except that 4 parts by weight of azodicarbonamide and 0.5 part by weight of zinc naphthenate were added to 0 parts by weight.
この絶縁電線の発泡度は約70%であり、しかも、発泡
絶縁体のワイヤストリッパによる剥取りは極めて容易で
あった。The foamed degree of this insulated wire was about 70%, and the foamed insulator was extremely easily peeled off by the wire stripper.
実施例6 低密度ポリエチレン(宇部興産UBEC−400)100重量部
にアゾジカルボンアミド3重量部およびヒドロキシステ
アリン酸亜鉛0.5重量部を添加した以外は実施例1と同
様にして発泡絶縁電線を製造した。Example 6 A foam insulated wire was produced in the same manner as in Example 1 except that 3 parts by weight of azodicarbonamide and 0.5 part by weight of zinc hydroxystearate were added to 100 parts by weight of low-density polyethylene (UBEC-400 manufactured by Ube Industries).
この絶縁電線の発泡度は約96%であり、しかも、発泡
絶縁体のワイヤストリッパによる剥取りは極めて容易で
あった。The foamed degree of this insulated wire was about 96%, and the foamed insulator was extremely easily peeled off by the wire stripper.
比較例1 低密度ポリエチレン(宇部興産UBEC−400)100重量部
にアゾジカルボンアミド3重量部を添加した組成物を用
いた以外は実施例1と同様にして発泡絶縁電線を製造し
た。Comparative Example 1 A foam insulated wire was produced in the same manner as in Example 1 except that a composition obtained by adding 3 parts by weight of azodicarbonamide to 100 parts by weight of low-density polyethylene (UBEC-400 manufactured by Ube Industries) was used.
この絶縁電線の発泡度は約70%であったが、導体と発
泡絶縁体が粘着し、発泡絶縁体のワイヤストリッパによ
る剥取りを行ったところ、導体上に発泡絶縁体が残っ
た。Although the degree of foaming of this insulated wire was about 70%, the conductor and the foamed insulator adhered to each other. When the foamed insulator was peeled off with a wire stripper, the foamed insulator remained on the conductor.
比較例2 低密度ポリエチレン(三井石油化学ミラソン3530)10
0重量部にアゾジカルボンアミド4重量部を添加した組
成物を用いた以外は実施例1と同様にして発泡絶縁電線
を製造した。Comparative Example 2 Low Density Polyethylene (Mitsui Petrochemical Mirason 3530) 10
A foam insulated wire was produced in the same manner as in Example 1 except that the composition in which 4 parts by weight of azodicarbonamide was added to 0 parts by weight.
この絶縁電線の発泡度は約76%であったが、導体と発
泡絶縁体が粘着し、発泡絶縁体のワイヤストリッパによ
る剥取りを行ったところ、導体上に発泡絶縁体が残っ
た。Although the foaming degree of this insulated wire was about 76%, the conductor and the foamed insulator adhered to each other. When the foamed insulator was peeled off with a wire stripper, the foamed insulator remained on the conductor.
比較例3 ステアリン酸亜鉛の添加量を8重量部とした以外は実
施例1と同様にして発泡絶縁電線を製造した。Comparative Example 3 A foam insulated wire was produced in the same manner as in Example 1 except that the amount of zinc stearate added was 8 parts by weight.
導体外周にコンパウンドを押出被覆する工程で発泡し
てしまい、絶縁電線の製造は不可能であった。It was impossible to manufacture an insulated wire because foaming occurred in the step of extrusion-coating the outer circumference of the conductor.
比較例4 リシノール酸亜鉛の添加量を8重量部とした以外は実
施例1と同様にして発泡絶縁電線を製造した。Comparative Example 4 A foam insulated wire was produced in the same manner as in Example 1 except that the amount of zinc ricinoleate added was 8 parts by weight.
導体外周にコンパウンドを押出被覆する工程で発泡し
てしまい、絶縁電線の製造は不可能であった。It was impossible to manufacture an insulated wire because foaming occurred in the step of extrusion-coating the outer circumference of the conductor.
比較例5 低密度ポリエチレン(三井石油化学ミラソン3530)10
0重量部にアゾジカルボンアミド3重量部およびシテア
リン酸0.5重量部を添加したコンパウンドを用いた以外
は実施例1と同様にして発泡絶縁電線を製造した。Comparative Example 5 Low-density polyethylene (Mitsui Petrochemical Mirason 3530) 10
A foam insulated wire was produced in the same manner as in Example 1 except that a compound obtained by adding 3 parts by weight of azodicarbonamide and 0.5 part by weight of citearic acid to 0 part by weight was used.
この絶縁電線の発泡度は約75%であったが、導体と発
泡絶縁体が粘着し、発泡絶縁体のワイヤストリッパによ
る剥取りを行ったところ、導体上に発泡絶縁体が残っ
た。The degree of foaming of this insulated wire was about 75%, but the conductor and the foamed insulation adhered to each other, and when the foamed insulation was stripped off with a wire stripper, the foamed insulation remained on the conductor.
[発明の効果] 以上説明してきた通り、本発明によれば高発泡化が可
能となり、しかも導体と発泡絶縁体との粘着を防止して
端末処理作業性を向上できる発泡絶縁電線を実現できる
ようになる。[Effects of the Invention] As described above, according to the present invention, it is possible to realize a foamed insulated wire that can be highly foamed and that can prevent sticking between a conductor and a foamed insulator to improve workability of terminal treatment. become.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 大窪 裕寿 茨城県日立市日高町5丁目1番1号 日立 電線株式会社電線研究所内 (72)発明者 浅井 孝康 茨城県日立市日高町5丁目1番1号 日立 電線株式会社日高工場内 (72)発明者 阿部 典元 茨城県日立市日高町5丁目1番1号 日立 電線株式会社日高工場内 (56)参考文献 特開 昭48−22559(JP,A) 特開 昭61−44933(JP,A) ─────────────────────────────────────────────────── ─── Continued front page (72) Inventor Hirotoshi Okubo 5-1-1 Hidaka-cho, Hitachi-shi, Ibaraki Electric Cable Research Laboratory, Hitachi Cable, Ltd. (72) Inventor Takayasu Asai 5 Hidaka-cho, Hitachi-shi, Ibaraki 1-1-1 Hitachi Cable Co., Ltd. Hidaka Plant (72) Inventor Norimoto Abe 5-1-1 Hidakacho, Hitachi City, Ibaraki Hitachi Cable Co., Ltd. Hidaka Plant (56) References 48-22559 (JP, A) JP-A-61-44933 (JP, A)
Claims (1)
カルボンアミド0.5〜15重量部および式Sn(OOCR)2で
示される亜鉛石鹸(Rは炭素数7以上のアルキル基)0.
05〜5重量部含有する樹脂組成物をアゾジカルボンアミ
ドの分解温度以下の温度で導体外周に押出被覆してから
電離性放射線の照射により架橋せしめ、しかる後アゾジ
カルボンアミドの分解温度以上に加熱して発泡絶縁体を
形成することを特徴とする発泡絶縁電線の製造方法。1. 0.5 to 15 parts by weight of azodicarbonamide and 100 parts by weight of polyolefin and zinc soap represented by the formula Sn (OOCR) 2 (R is an alkyl group having 7 or more carbon atoms).
The resin composition containing 05 to 5 parts by weight is extrusion-coated on the outer circumference of the conductor at a temperature not higher than the decomposition temperature of azodicarbonamide, and then crosslinked by irradiation of ionizing radiation, and then heated to a temperature not lower than the decomposition temperature of azodicarbonamide. A method for producing a foam insulated wire, comprising forming a foam insulator.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62053700A JPH0824015B2 (en) | 1987-01-08 | 1987-03-09 | Method for manufacturing foam insulated wire |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP211287 | 1987-01-08 | ||
| JP62-2112 | 1987-01-08 | ||
| JP62053700A JPH0824015B2 (en) | 1987-01-08 | 1987-03-09 | Method for manufacturing foam insulated wire |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63304533A JPS63304533A (en) | 1988-12-12 |
| JPH0824015B2 true JPH0824015B2 (en) | 1996-03-06 |
Family
ID=26335431
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62053700A Expired - Fee Related JPH0824015B2 (en) | 1987-01-08 | 1987-03-09 | Method for manufacturing foam insulated wire |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0824015B2 (en) |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6144933A (en) * | 1984-08-10 | 1986-03-04 | Hatsupoo Kagaku Kogyo Kk | Flame-retarding resin composition for extrusion foaming |
-
1987
- 1987-03-09 JP JP62053700A patent/JPH0824015B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63304533A (en) | 1988-12-12 |
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