JPS58100313A - Laminated sheath electric cable for atomic power generation plant - Google Patents
Laminated sheath electric cable for atomic power generation plantInfo
- Publication number
- JPS58100313A JPS58100313A JP56196555A JP19655581A JPS58100313A JP S58100313 A JPS58100313 A JP S58100313A JP 56196555 A JP56196555 A JP 56196555A JP 19655581 A JP19655581 A JP 19655581A JP S58100313 A JPS58100313 A JP S58100313A
- Authority
- JP
- Japan
- Prior art keywords
- laminated
- electric cable
- tape
- power generation
- cable
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000010248 power generation Methods 0.000 title 1
- 229910052751 metal Inorganic materials 0.000 claims description 18
- 239000002184 metal Substances 0.000 claims description 18
- 229920000098 polyolefin Polymers 0.000 claims description 10
- 230000005855 radiation Effects 0.000 claims description 10
- 229920005989 resin Polymers 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 8
- 229910000077 silane Inorganic materials 0.000 claims description 6
- -1 silane compound Chemical class 0.000 claims description 6
- 150000001491 aromatic compounds Chemical class 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 2
- 150000002391 heterocyclic compounds Chemical class 0.000 claims description 2
- 238000010030 laminating Methods 0.000 claims 1
- 239000000463 material Substances 0.000 description 8
- 230000015556 catabolic process Effects 0.000 description 7
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 239000004020 conductor Substances 0.000 description 6
- 239000002826 coolant Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000011241 protective layer Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 230000006866 deterioration Effects 0.000 description 5
- 238000009413 insulation Methods 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000011810 insulating material Substances 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 2
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 2
- 230000005251 gamma ray Effects 0.000 description 2
- 229920002681 hypalon Polymers 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- UJMCQPQGRLFHGD-UHFFFAOYSA-N 1,2,3-tripropylfluoranthene Chemical compound C12=CC=CC=C2C2=CC=CC3=C2C1=C(CCC)C(CCC)=C3CCC UJMCQPQGRLFHGD-UHFFFAOYSA-N 0.000 description 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- MSYRKNADCLYPAU-UHFFFAOYSA-N 1-propylfluoranthene Chemical compound C1=CC=C2C3=CC=CC=C3C3=C2C1=CC=C3CCC MSYRKNADCLYPAU-UHFFFAOYSA-N 0.000 description 1
- ZNRLMGFXSPUZNR-UHFFFAOYSA-N 2,2,4-trimethyl-1h-quinoline Chemical compound C1=CC=C2C(C)=CC(C)(C)NC2=C1 ZNRLMGFXSPUZNR-UHFFFAOYSA-N 0.000 description 1
- 206010000369 Accident Diseases 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- NOZAQBYNLKNDRT-UHFFFAOYSA-N [diacetyloxy(ethenyl)silyl] acetate Chemical compound CC(=O)O[Si](OC(C)=O)(OC(C)=O)C=C NOZAQBYNLKNDRT-UHFFFAOYSA-N 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000010692 aromatic oil Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- QHZOMAXECYYXGP-UHFFFAOYSA-N ethene;prop-2-enoic acid Chemical compound C=C.OC(=O)C=C QHZOMAXECYYXGP-UHFFFAOYSA-N 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- 238000010559 graft polymerization reaction Methods 0.000 description 1
- 229920001112 grafted polyolefin Polymers 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- BYOIQYHAYWYSCZ-UHFFFAOYSA-N prop-2-enoxysilane Chemical compound [SiH3]OCC=C BYOIQYHAYWYSCZ-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000004250 tert-Butylhydroquinone Substances 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A30/00—Adapting or protecting infrastructure or their operation
- Y02A30/14—Extreme weather resilient electric power supply systems, e.g. strengthening power lines or underground power cables
Landscapes
- Insulated Conductors (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は原子力発電所ラミネートシース電気ケーブルに
係り、特に金属テープにラミネートする樹脂として耐放
射線性架橋ポリオレフィンを用いたラミネートシース電
気ケーブルに関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a laminated sheathed electric cable for a nuclear power plant, and more particularly to a laminated sheathed electric cable using a radiation-resistant crosslinked polyolefin as a resin laminated to a metal tape.
軽水炉型原子力発電所で使用されるケーブルは、常時熱
と放射線に曝され、これに加え、冷却材喪失事故時に、
沸騰水型原子炉(BWR)では高温水蒸気に、加圧水型
原子炉(PWR)では高温水蒸気とホウ酸やカセイソー
ダからなる化学液に曝されてもケーブルとしての機能を
保持するもので−なければならない。Cables used in light water reactor nuclear power plants are constantly exposed to heat and radiation, and in addition, in the event of a loss of coolant accident,
It must maintain its function as a cable even when exposed to high-temperature steam in a boiling water reactor (BWR) or to high-temperature steam and a chemical solution consisting of boric acid or caustic soda in a pressurized water reactor (PWR). .
このため、これらのケーブルに使用される絶縁やシース
材料は、耐熱性、耐放射線性および耐水蒸気性などを兼
ね備えていなければならない。その上、火災事故時を想
定し、高度の離燃性が要求される。Therefore, the insulation and sheath materials used in these cables must have heat resistance, radiation resistance, water vapor resistance, and the like. Furthermore, a high degree of flammability is required in case of a fire accident.
ところで、従来、絶縁材料およびシース材料はこれらの
目□的に適合させるため、高分子材料をペースとしてこ
れに添加する添加剤とその量を選択することで対処する
方法がとられていた。By the way, conventionally, in order to make the insulating material and the sheath material compatible with these objectives, a method has been taken in which the additives added to the polymeric material as a paste and the amount thereof are selected.
しかし、高分子材料のみで絶縁材料およびシース材料を
構成したケーブル構成では、熱劣化、γ線照射および高
温水蒸気に曝された場合、これら高分子材料の機械的特
性が大きく低下し、また、交流破壊電圧などの電気的特
性が著しく低下するという問題を生ずる。However, in a cable configuration in which the insulating material and sheath material are composed only of polymeric materials, the mechanical properties of these polymeric materials deteriorate significantly when exposed to thermal deterioration, gamma ray irradiation, and high-temperature steam, and A problem arises in that electrical characteristics such as breakdown voltage are significantly reduced.
本発明は上記に鑑みてなされたもので、その目的とする
ところは、熱、−放射線および化学液を含む高温水蒸気
に曝されても交流破壊電圧などの電気的特性の低下を大
幅に抑制することができる原子力発電所用ラミネートシ
ース電気ケーブルを提供することにある。The present invention has been made in view of the above, and its purpose is to significantly suppress the deterioration of electrical characteristics such as AC breakdown voltage even when exposed to heat, radiation, and high-temperature steam containing chemical liquids. The object of the present invention is to provide a laminated sheathed electric cable for nuclear power plants that can be used in nuclear power plants.
本発明の特徴は、ポリオレフィンにシラン化合物、芳香
族化合物あるいは複素種化合物のうち1攬以上とラジカ
ル発生剤とを加えて加熱反応させて得た耐放射線性水架
橋シラングラフトポリオレフィンを金属テープにラミネ
ートしたラミネートテープで遮蔽層を形成した電気ケー
ブルとした点にある。A feature of the present invention is that radiation-resistant water-crosslinked silane grafted polyolefin obtained by adding at least one of a silane compound, an aromatic compound, or a complex compound and a radical generator to a polyolefin and causing a heating reaction is laminated onto a metal tape. The electrical cable has a shielding layer made of laminated tape.
本発明において、金属テープにラミネートする樹脂とし
て耐放射線性水架橋シランクラフトポリオレフィンを用
いた理由は、一般にラミネートシース電気ケーブルに用
いられている樹脂は耐放射線性に劣り、放射線照射後接
着強さが極端に低下し、高温水蒸気に曝されるとシース
材料を通して水蒸気が絶縁材料にまで達し、電気的特性
を大幅に低下させるだめ、これを防止するためである。In the present invention, the reason why radiation-resistant water-crosslinked silane craft polyolefin was used as the resin to be laminated to the metal tape is that resins generally used for laminated sheathed electric cables have poor radiation resistance, and the adhesive strength after irradiation is poor. This is to prevent this from occurring, since if the temperature drops to an extremely high temperature and the insulation material is exposed to high-temperature water vapor, the water vapor will reach the insulating material through the sheath material, significantly reducing the electrical characteristics.
ここに、ポリオレフィンとは、オレフィンポリ又または
オレフィンを含むコポリマであり、ポリエチレン、エチ
レン、酢酸ビニル共重合体、エチレン・アクリル酸また
はそのエステルとの共重合体、エチレン・プロピレン(
またはジエンモノマ)共重合体、エチレン−α−オレフ
ィンコポリマ、エチレン・ブチレン共重合体、へロヂン
化ポリオレフィンあるいはそれらに塩化ビニルモノマを
グラフト重合させたものなど含む。Here, polyolefin refers to an olefin poly or a copolymer containing an olefin, such as polyethylene, ethylene, vinyl acetate copolymer, copolymer of ethylene/acrylic acid or its ester, ethylene/propylene (
or diene monomer) copolymers, ethylene-α-olefin copolymers, ethylene-butylene copolymers, herodinated polyolefins, and those obtained by graft polymerization of vinyl chloride monomers.
また、シラン化合物は、加水分解可能な有機基例えば、
メトキシ基、エトキシ基およびブトキシ基等のアルコキ
ン基を含み、かつ、重合体中に発生した遊離ラジカル部
位と反応性である脂肪族的に不飽和な炭化水素基ま、た
けハイドロカーボンオキシ基を有する化合物が好適であ
り、その代表例として線、ビニルトリメトキシシラン、
ビニルトリエトキシシランおよびビニルトリアセトキシ
シランなどが挙げられる。In addition, the silane compound has hydrolyzable organic groups such as
Aliphatically unsaturated hydrocarbon groups containing alkoxy groups such as methoxy, ethoxy, and butoxy groups, and which are reactive with free radical sites generated in the polymer; Compounds are preferred, representative examples of which are silane, vinyltrimethoxysilane,
Examples include vinyltriethoxysilane and vinyltriacetoxysilane.
また、芳香族化合物とは、フェノール系、アミン系、イ
オウ、リン系に代表される酸化防止剤、ゴムの操作油と
して使用される芳香族油などで、例えば、2.5−Di
−第3ブチルヒドロキノン、N、%−1フェニルーP−
フェニレンジアミン、プロピルフルオランセルを挙げる
ことができる。Aromatic compounds include antioxidants such as phenol, amine, sulfur, and phosphorus, and aromatic oils used as operating oils for rubber, such as 2.5-Di
-Tertiary butylhydroquinone, N,%-1 phenyl-P-
Examples include phenylenediamine and propylfluorancel.
複素環化合物としては、例えば、トリアジン誘導体、2
.2.4−トリメチル−1,2−ジヒドロキノリンを挙
げることができる。Examples of the heterocyclic compound include triazine derivatives, 2
.. Mention may be made of 2,4-trimethyl-1,2-dihydroquinoline.
また、ラジカル発生剤としては、ジクミルパーオキサイ
ド、過酸化ベンゾイル、2.5−ジメチル−2,5−:
)(第5ブチル、ペルオキシ)ヘキンン−3などの有機
過酸化物、アゾビスイソブチロニトリルおよびジメチル
アゾイソブチレートなどのアゾ化合物を挙げることがで
きる。In addition, as a radical generator, dicumyl peroxide, benzoyl peroxide, 2,5-dimethyl-2,5-:
) (5-butyl, peroxy)hequin-3, azo compounds such as azobisisobutyronitrile and dimethylazoisobutyrate.
本発明における化学反応の進行にあたっては、必要に応
じ、一般にシロキサン縮合触媒として、ジブチル・スズ
・ジラウレート、ジブチル・スズジオクタエート、ナフ
テン酸鉛などのはかにエチルアミン、ジブチルアミンお
よびヘキシルアミンなどの有機塩基が用いられる。ただ
し、縮合触媒の添加により架橋密度が高くなり過ぎると
、金属テープとの接着力が低下するので注意を要する。In the progress of the chemical reaction in the present invention, as a siloxane condensation catalyst, dibutyl tin dilaurate, dibutyl tin dioctaate, lead naphthenate, etc., ethylamine, dibutylamine, hexylamine, etc. are generally used as a siloxane condensation catalyst. Organic bases are used. However, care must be taken because if the crosslinking density becomes too high due to the addition of a condensation catalyst, the adhesive strength with the metal tape will decrease.
さらに、架橋ポリオレフィンには、本発明の効果を阻害
しないような酸化防止剤、金属害抑制剤柴外線吸収剤、
着色剤など種々の配合剤を使用しても差し支えない。Furthermore, the cross-linked polyolefin may include antioxidants, metal damage inhibitors, and ray absorbers that do not inhibit the effects of the present invention.
Various additives such as coloring agents may be used.
本発明に使用し得る金属は、周期律表第tb、nb■、
■、■および■族の金属である。好ましい金属は、鉄、
アルミニウム、亜鉛、スズ、銅、鉛などや黄銅や鋼のよ
うなこれらの金属の合金などのある。なお、金属の表面
は注意深く浄化し、グリス、汚れ、その他の有機物の残
渣を除去しておくことが好ましい。Metals that can be used in the present invention include metals from periodic table tb, nb■,
Metals of the ■, ■, and ■ groups. Preferred metals are iron,
These include aluminum, zinc, tin, copper, lead, etc. and alloys of these metals such as brass and steel. It is preferred that the metal surface be carefully cleaned to remove grease, dirt, and other organic residues.
本発明に係るラミネートテープの製造方法は、積層法、
塗装法あるいは両者の組合せなどの任意の方法によって
行うことができる。例えば、積層法においては、押出機
または塗装機により連続的にポリオレフィンを金属テー
プ上にラミネートする0その他フィルム状物の代りにペ
レット、粉末などを使用することもできる。The method for producing a laminate tape according to the present invention includes a lamination method,
This can be done by any method such as painting or a combination of both. For example, in the lamination method, polyolefin is continuously laminated onto a metal tape using an extruder or a coating machine.In addition, pellets, powder, etc. can also be used instead of a film-like material.
次に本発明の実施例および参考のための比較例について
説明する。Next, examples of the present invention and comparative examples for reference will be described.
実施例1
密度a934f/cII、溶融指数K Of710mi
nの中密度ポリエチレン100重量部に対して、ビニル
メトキシシランを1.5重量部、ジクミルパーオキサイ
ドをα15重量部、プロピルフルオランセンを3重量部
、ポリ−2,2,4−トリメチル−12−ジヒドロキノ
リンをα1重量部加え、ヘンシェルミキサーにより70
℃にて5分間攪拌含浸した彼、40■押出機により23
−0 ℃でT−ダイを用いて軟アルミニウム(厚さ0.
2冒)上に0.05■の厚さに押出し、このラミネート
テープを用いてエチレン自フロピレンゴム絶縁、クロロ
スルホン化ポリエチレン外部保護層からなる電気ケーブ
ル(導体!SX!L5−)を製作した。Example 1 Density a934f/cII, melting index K Of710mi
n medium density polyethylene, 1.5 parts by weight of vinylmethoxysilane, 15 parts by weight of dicumyl peroxide, 3 parts by weight of propylfluoranthene, poly-2,2,4-trimethyl- Add α1 part by weight of 12-dihydroquinoline and mix with a Henschel mixer to 70%
Stir impregnated for 5 minutes at 40°C and 23°C by extruder.
Soft aluminum (thickness:
2) The laminated tape was extruded to a thickness of 0.05 cm and used to produce an electric cable (conductor! SX! L5-) consisting of an ethylene autofluoropylene rubber insulation and a chlorosulfonated polyethylene outer protective layer.
冑施flJ 2
密度α88t/cd、溶鵬指数゛21口f/10m1n
のエチレン・プロピレン共重合体(エチレン含有量8゜
l1b)100重量部に対して、ビニルメトキノンラン
を2重量部、ジクミルパーオキサイドを0.2重量部、
プロピル7ケオランセンt−2重量部、ポリ−2,2,
4−トリメチル1.2−ジヒドロキノリンを0.1重量
部加え、ヘンシェルミキサーにょシフ0℃にて5分間攪
拌含浸した後、40■押出機により230℃でTダイを
用いて軟アルミニウム(厚さ0.21111 )上K
a O5wi、の厚さに押出し、このラミネートテープ
を用いてエチレン・プロピレンゴム絶縁、クロロプレン
外部保護層からなる電気ケーブル(導体3X5.5−)
を製作した。Dense flJ 2 Density α88t/cd, Weld index ゛21f/10m1n
For 100 parts by weight of ethylene propylene copolymer (ethylene content 8゜l1b), 2 parts by weight of vinylmethquinonelan, 0.2 parts by weight of dicumyl peroxide,
Propyl 7keolanthene t-2 parts by weight, poly-2,2,
0.1 part by weight of 4-trimethyl 1,2-dihydroquinoline was added, stirred and impregnated in a Henschel mixer at 0°C for 5 minutes. 0.21111) upper K
Extruded to a thickness of O5wi, this laminated tape was used to make an electric cable (conductor 3x5.5-) consisting of ethylene/propylene rubber insulation and chloroprene outer protective layer.
was produced.
奥fa例3
密度α88〜α89 f/d、溶融指数3〜5F/IQ
min(190℃)の低結晶性ポリオレフィン樹脂10
0重量部に対し才、ビニルトリメトキシンランを2重量
部、ジクミルパーオキサイドをα2重量部、トリプロピ
ルフルオランセンを2重量部、ポリ−2,2,4−トリ
メチル−1,2−ジヒドロキノリンを0.1重量を加え
、ヘンシェルミキサーにより70℃にて5分間攪拌含浸
した後、4o■押出機により230℃でTダイを用いて
軟アルミニウム(厚さ0.2■)上にO,OS鱈の厚さ
に押出し、このラミネートテープを用いてエチレンプロ
ピレンゴム絶縁、塩素化ポリエチレン外部保護層からな
る電気ケーブル(導体3X5.5−)を製作した。Back fa example 3 Density α88~α89 f/d, melting index 3~5F/IQ
min (190°C) low crystalline polyolefin resin 10
0 parts by weight, 2 parts by weight of vinyl trimethoxine, 2 parts by weight of dicumyl peroxide, 2 parts by weight of tripropylfluoranthene, poly-2,2,4-trimethyl-1,2-dihydro After adding 0.1 weight of quinoline and stirring and impregnating it at 70°C for 5 minutes using a Henschel mixer, O, The laminated tape was extruded to the thickness of OS cod, and an electric cable (conductor 3 x 5.5-) consisting of ethylene propylene rubber insulation and chlorinated polyethylene outer protective layer was manufactured using this laminated tape.
比較例
40■押出機により250℃でTダイを用いて反応性カ
ルボキシル基を含むポリオレフィン共重合体を軟化アル
ミニウム(厚さ0.2 wm )上に0.05■の厚さ
に押出し、このラミネートテープを用いてエチレンフロ
ピレンゴム絶縁、クロロスルホン化ポリエチレン外部保
護層からなる電気ケーブル(導体3xs、sj)を製作
した。Comparative Example 40 ■ A polyolefin copolymer containing a reactive carboxyl group was extruded onto softened aluminum (thickness 0.2 wm) to a thickness of 0.05 ■ using an extruder at 250°C using a T-die, and this laminate was An electric cable (conductor 3xs, sj) consisting of ethylene fluoropylene rubber insulation and a chlorosulfonated polyethylene outer protective layer was manufactured using tape.
なお、一般にラミネートシース電気ケーブルは金属とし
てアルミニウムテープが使用されているので、各実施例
、比較例とも金属テープとしてアルミニウムテープを用
いた。第1図は本発明のラミネートシース電気ケーブル
の一実施例を示す断面図で、第1図において、100は
ケーブルコアであり、1は導体、2は絶縁体である。1
oがラミネートテープであり、3心のケーブルコアを縦
沿え包被しており、3は金属テープ、4はラミネート樹
脂層である。5は合成樹脂の外部保護層を示す。Note that since aluminum tape is generally used as the metal in laminated sheathed electric cables, aluminum tape was used as the metal tape in both Examples and Comparative Examples. FIG. 1 is a sectional view showing an embodiment of the laminated sheathed electric cable of the present invention. In FIG. 1, 100 is a cable core, 1 is a conductor, and 2 is an insulator. 1
o is a laminate tape that covers the three cable cores vertically, 3 is a metal tape, and 4 is a laminate resin layer. 5 indicates an outer protective layer of synthetic resin.
次に1上記した各実施例および比較例により得られたラ
ミネートテープの接着強さと、それを用いた電気ケーブ
ルの交流破壊電圧を調べた。第2図はラミネートテープ
の接着強さの試験方法の説明図で、6はアルミニウムテ
ープ、7Fiラミネ一ト樹脂層で、図示の状態で、図示
矢印方向へ引張速度100m/分で引張ったときの引張
り力を測定した。そのときの条件は、初期、121℃で
7日間熱劣化した後、その後にさらにγ線照射(200
Mrad)後、その後さらに冷却材曝露後の4つとした
。冷却材曝露は第3図に示す温度と時間の関係にな−る
ようにした。なお、最初の24時間は化学スプレーを同
時に行った。また、ケーブルの交流破壊電圧の測定は昇
圧速度500 V/seeとして行った。Next, the adhesive strength of the laminate tapes obtained in each of the above-mentioned Examples and Comparative Examples and the AC breakdown voltage of an electric cable using the same were investigated. Figure 2 is an explanatory diagram of the method for testing the adhesive strength of laminated tapes, where 6 is an aluminum tape and 7Fi laminated resin layer is pulled in the direction shown by the arrow at a pulling speed of 100 m/min in the state shown in the figure. The tensile force was measured. The conditions at that time were initial thermal deterioration at 121°C for 7 days, followed by further gamma ray irradiation (200°C).
Mrad) and then four after coolant exposure. The coolant exposure was made to have the relationship between temperature and time shown in Figure 3. Note that chemical spraying was performed at the same time for the first 24 hours. Further, the AC breakdown voltage of the cable was measured at a boost rate of 500 V/see.
々お、交流破壊電圧測定時のケーブルの条件は上記と同
様とした。11g1表はその結果を示す。The cable conditions when measuring AC breakdown voltage were the same as above. Table 11g1 shows the results.
第 1 表
第1表の結果かられかるように、比較例では、熱劣化→
γ線照射後のラミネートテープの接着強さが大幅に低下
し、その後冷却材に曝露するとラミネートテープとして
の機能を失う。そのため、ケーブルの交流破壊電圧はx
otv以下と著しく低下している。これに対し、実施例
1〜3はいずれも耐放射線性を示し、冷却材曝露後も極
めて良好な電気的特性を示す。Table 1 As can be seen from the results in Table 1, in the comparative example, thermal deterioration→
After irradiation with gamma rays, the adhesive strength of the laminated tape decreases significantly, and it loses its functionality as a laminated tape when subsequently exposed to coolant. Therefore, the AC breakdown voltage of the cable is x
It has significantly decreased below OTV. On the other hand, Examples 1 to 3 all exhibit radiation resistance and exhibit extremely good electrical characteristics even after exposure to coolant.
なお、電気ケーブルの屈曲性を増すため、ラミネートテ
ープを横巻きにしてもよく、また、コルゲートタイプと
してもよく、それによって効果が変ることはない。In addition, in order to increase the flexibility of the electric cable, the laminated tape may be wound horizontally or may be of a corrugated type, but the effect will not change.
以上説明したように、本発明によれば、熱、放射線およ
び化学液を含む高温水蒸気に曝されても交流破壊電圧な
どの電気的特性の低下を大幅に抑制することができると
いう効果がある。As explained above, according to the present invention, there is an effect that deterioration of electrical characteristics such as AC breakdown voltage can be significantly suppressed even when exposed to heat, radiation, and high-temperature steam containing chemical liquid.
第1−は本発明の原子力発電所用ラミネートシース電気
ケーブルの一実施例を示す断面図、第2図はラミネート
テープの接着強さの試験方法の説明図、第3図仲冷却材
曝露試験における温度プロファイルを示す図である。
100・・・・・・ケーブルコア、1・・・・・・導体
、2・・・・・・絶縁体、10・・・・・・ラミネート
テープ、3・・・・・・金属テープ、4・・・・・・ラ
ミネート樹脂層、5・・・・・・外部保護層。Figure 1- is a cross-sectional view showing one embodiment of the laminated sheathed electric cable for nuclear power plants of the present invention, Figure 2 is an explanatory diagram of the method for testing the adhesive strength of laminated tape, and Figure 3 is the temperature in the intermediate coolant exposure test. It is a figure showing a profile. 100... Cable core, 1... Conductor, 2... Insulator, 10... Laminated tape, 3... Metal tape, 4 ... Laminate resin layer, 5 ... External protective layer.
Claims (1)
ープを遮蔽層として使用したラミネートシース電気ケー
ブルにおいて、前記金属テープにラミネートする樹脂と
してポリオレフィンにシラン化合物、芳香族化合物ある
いは複素環化合物のうち1種以上とラジカル発生剤とを
加えて加熱反応させて得た耐放射線性水架橋シラングラ
ットポリオレフィ/を用いであることを特徴とする原子
力発電所用電気ケーブル。1. In a laminated sheathed electric cable using a laminate tape obtained by laminating a resin on a metal tape as a shielding layer, the resin laminated to the metal tape includes polyolefin and one or more of a silane compound, an aromatic compound, or a heterocyclic compound. An electric cable for a nuclear power plant, characterized in that it uses a radiation-resistant water-crosslinked silanglat polyolefin obtained by heating and reacting with a radical generator.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56196555A JPS58100313A (en) | 1981-12-07 | 1981-12-07 | Laminated sheath electric cable for atomic power generation plant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56196555A JPS58100313A (en) | 1981-12-07 | 1981-12-07 | Laminated sheath electric cable for atomic power generation plant |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58100313A true JPS58100313A (en) | 1983-06-15 |
| JPS6231447B2 JPS6231447B2 (en) | 1987-07-08 |
Family
ID=16359677
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56196555A Granted JPS58100313A (en) | 1981-12-07 | 1981-12-07 | Laminated sheath electric cable for atomic power generation plant |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58100313A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103871600A (en) * | 2014-02-27 | 2014-06-18 | 安徽复兴电缆集团有限公司 | Power cable used for nuclear power plant |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5448088A (en) * | 1977-09-26 | 1979-04-16 | Showa Electric Wire & Cable Co | Electric cable |
-
1981
- 1981-12-07 JP JP56196555A patent/JPS58100313A/en active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5448088A (en) * | 1977-09-26 | 1979-04-16 | Showa Electric Wire & Cable Co | Electric cable |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103871600A (en) * | 2014-02-27 | 2014-06-18 | 安徽复兴电缆集团有限公司 | Power cable used for nuclear power plant |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6231447B2 (en) | 1987-07-08 |
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