JP2012182036A - Insulation wire - Google Patents
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- JP2012182036A JP2012182036A JP2011044618A JP2011044618A JP2012182036A JP 2012182036 A JP2012182036 A JP 2012182036A JP 2011044618 A JP2011044618 A JP 2011044618A JP 2011044618 A JP2011044618 A JP 2011044618A JP 2012182036 A JP2012182036 A JP 2012182036A
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- derived polyamide
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- 238000009413 insulation Methods 0.000 title abstract description 7
- 229920005989 resin Polymers 0.000 claims abstract description 31
- 239000011347 resin Substances 0.000 claims abstract description 31
- 239000004952 Polyamide Substances 0.000 claims abstract description 30
- 229920002647 polyamide Polymers 0.000 claims abstract description 30
- 239000012212 insulator Substances 0.000 claims abstract description 18
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000004020 conductor Substances 0.000 claims abstract description 13
- 239000000155 melt Substances 0.000 claims abstract description 9
- 239000011342 resin composition Substances 0.000 claims abstract description 7
- GUOSQNAUYHMCRU-UHFFFAOYSA-N 11-Aminoundecanoic acid Chemical compound NCCCCCCCCCCC(O)=O GUOSQNAUYHMCRU-UHFFFAOYSA-N 0.000 claims description 3
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- 239000002028 Biomass Substances 0.000 abstract description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 20
- 230000007613 environmental effect Effects 0.000 abstract description 8
- 241000196324 Embryophyta Species 0.000 description 24
- 239000000203 mixture Substances 0.000 description 21
- 229920003023 plastic Polymers 0.000 description 11
- 239000004033 plastic Substances 0.000 description 11
- -1 polyethylene Polymers 0.000 description 11
- 239000003063 flame retardant Substances 0.000 description 8
- 239000000654 additive Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 5
- 229920001155 polypropylene Polymers 0.000 description 5
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 4
- 229920000747 poly(lactic acid) Polymers 0.000 description 4
- 239000004626 polylactic acid Substances 0.000 description 4
- 238000010998 test method Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 229920002301 cellulose acetate Polymers 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229920002961 polybutylene succinate Polymers 0.000 description 3
- 239000004631 polybutylene succinate Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 239000010779 crude oil Substances 0.000 description 2
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 2
- 229960001826 dimethylphthalate Drugs 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- LLVVSBBXENOOQY-UHFFFAOYSA-N 1,2,3,4,5-pentabromobenzene Chemical compound BrC1=CC(Br)=C(Br)C(Br)=C1Br LLVVSBBXENOOQY-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- PIABECBOMBVJHV-UHFFFAOYSA-N BrC1=C(C(=C(C=C1)Br)Br)Br.BrC1=C(C(=C(C=C1)Br)Br)Br.C=C Chemical compound BrC1=C(C(=C(C=C1)Br)Br)Br.BrC1=C(C(=C(C=C1)Br)Br)Br.C=C PIABECBOMBVJHV-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 102100035474 DNA polymerase kappa Human genes 0.000 description 1
- 101710108091 DNA polymerase kappa Proteins 0.000 description 1
- 239000004803 Di-2ethylhexylphthalate Substances 0.000 description 1
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004712 Metallocene polyethylene (PE-MC) Substances 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- 240000000528 Ricinus communis Species 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 1
- 239000005042 ethylene-ethyl acrylate Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 239000003112 inhibitor 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
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000029553 photosynthesis Effects 0.000 description 1
- 238000010672 photosynthesis Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920005629 polypropylene homopolymer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Insulated Conductors (AREA)
Abstract
Description
本発明は、絶縁電線に関するものであり、さらに詳しくは、自動車、電気・電子機器等に好適な絶縁電線に関するものである。 The present invention relates to an insulated wire, and more particularly to an insulated wire suitable for automobiles, electrical / electronic devices, and the like.
従来から、例えば自動車や電気・電子機器等に配線される絶縁電線には、ポリオレフィンなどの化石資源(石油資源)を原料とする樹脂を絶縁体(絶縁被覆)に用いたものが知られている。周知の通り、化石資源は限りある資源である。また、化石資源から生産された製品を焼却廃棄すると、大気中のCO2濃度の上昇に繋がる。 2. Description of the Related Art Conventionally, for insulated wires wired to automobiles, electric / electronic devices, and the like, those using a resin made of fossil resources (petroleum resources) such as polyolefin as an insulator (insulation coating) are known. . As is well known, fossil resources are limited resources. In addition, incineration and disposal of products produced from fossil resources will lead to an increase in atmospheric CO 2 concentration.
最近、地球環境への配慮から、バイオマス資源が注目されている。バイオマス資源は、植物等の現生生物由来の、比較的短期間で再生可能な資源である。また、バイオマス資源に含まれる炭素は、そのバイオマスが成長過程で光合成により大気中から吸収されたCO2に由来するため、バイオマス資源は大気中のCO2濃度のバランスを維持する面を有する。さらに、バイオマス資源の多くは生分解性を有するため、バイオマス資源から生産されたバイオマスプラスチック製品は、使用後に埋め立て処理できる場合がある。なにより、バイオマス資源を用いることで化石資源の使用量を低減できる。したがって、バイオマス資源を用いることにより、環境負荷の低減を図ることができる。 Recently, biomass resources have attracted attention because of consideration for the global environment. Biomass resources are resources that can be regenerated in a relatively short period of time, derived from modern organisms such as plants. Moreover, since carbon contained in biomass resources is derived from CO 2 absorbed from the atmosphere by photosynthesis during the growth process, the biomass resources have a surface that maintains a balance of CO 2 concentration in the atmosphere. Furthermore, since many biomass resources are biodegradable, biomass plastic products produced from biomass resources may be landfilled after use. Above all, the use of fossil resources can be reduced by using biomass resources. Therefore, environmental load can be reduced by using biomass resources.
従来、このようなバイオマスプラスチックは、その機械特性から、主に成形部品に用いる試みはなされているものの、自動車等の電線分野で用いる試みはあまりなされていない(特許文献1など)。 Conventionally, such biomass plastics have been attempted mainly for use in molded parts due to their mechanical properties, but not much attempts have been made in the field of electric wires such as automobiles (Patent Document 1, etc.).
自動車等の電線分野でバイオマスプラスチックを用いる場合には、電線を配策する場所の特殊性から、電線として求められる各種機械特性の他、耐水性を備えていることが求められる。しかしながら、バイオマスプラスチックは、ポリエステルやセルロースからなるものが多く、これらのものは、その分子構造から十分な耐水性を備えていないのが現状である。 When using biomass plastic in the field of electric wires such as automobiles, it is required to have water resistance in addition to various mechanical properties required for electric wires because of the particularity of the location where the electric wires are routed. However, many biomass plastics are made of polyester or cellulose, and the present situation is that these plastics do not have sufficient water resistance due to their molecular structure.
本発明が解決しようとする課題は、再生可能なバイオマス資源を用いて環境負荷の低減を図るとともに、バイオマス資源を用いた場合においても耐水性に優れる絶縁電線を提供することにある。 The problem to be solved by the present invention is to provide an insulated wire that is excellent in water resistance even when a biomass resource is used while reducing the environmental load using a renewable biomass resource.
上記課題を解決するため本発明に係る絶縁電線は、導体と、前記導体の外周を被覆する絶縁体とを備えた絶縁電線において、前記絶縁体が、植物由来のポリアミドと塩化ビニル樹脂とを含有する樹脂組成物よりなることを要旨とするものである。 In order to solve the above problems, an insulated wire according to the present invention is an insulated wire comprising a conductor and an insulator covering the outer periphery of the conductor, wherein the insulator contains a plant-derived polyamide and a vinyl chloride resin. The gist of the invention is that it comprises a resin composition.
この際、前記植物由来のポリアミドのASTM D1238に準拠して測定される230℃、21.18Nにおけるメルトフローレイトが0.1〜50g/10分の範囲内であることが好ましい。 Under the present circumstances, it is preferable that the melt flow rate in 230 degreeC and 21.18N measured based on ASTM D1238 of the said plant-derived polyamide exists in the range of 0.1-50 g / 10min.
本発明に係る絶縁電線によれば、植物由来のポリアミドと塩化ビニル樹脂とを含有する樹脂組成物により絶縁体が構成されているため、環境負荷の低減を図ることができる。また、この植物由来のポリアミドは、ポリエステルやセルロースからなるバイオマスプラスチックとは異なり、加水分解しにくく、耐水性を有する。したがって、バイオマスプラスチックを用いた場合においても耐水性に優れる。 According to the insulated wire according to the present invention, since the insulator is composed of the resin composition containing the plant-derived polyamide and the vinyl chloride resin, it is possible to reduce the environmental load. Moreover, unlike the biomass plastic which consists of polyester and a cellulose, this plant-derived polyamide is hard to hydrolyze and has water resistance. Therefore, even when biomass plastic is used, the water resistance is excellent.
この際、植物由来のポリアミドのASTM D1238に準拠して測定される230℃、21.18Nにおけるメルトフローレイトが特定の範囲内であると、ともに用いる塩化ビニル樹脂との相溶性が高くなるため、耐寒性を低下させにくくできる。 At this time, if the melt flow rate at 230 ° C. and 21.18 N measured in accordance with ASTM D1238 of the plant-derived polyamide is within a specific range, the compatibility with the vinyl chloride resin used together increases, It is difficult to reduce cold resistance.
次に、本発明の実施形態について詳細に説明する。 Next, an embodiment of the present invention will be described in detail.
本発明に係る絶縁電線は、導体と、この導体の外周を被覆する絶縁体とを備える。導体は、金属線、金属撚線などにより構成される。導体の金属としては、銅、銅合金、アルミニウム、アルミニウム合金などを挙げることができる。 The insulated wire according to the present invention includes a conductor and an insulator covering the outer periphery of the conductor. The conductor is composed of a metal wire, a metal stranded wire, or the like. Examples of the metal of the conductor include copper, copper alloy, aluminum, and aluminum alloy.
絶縁体は、植物由来のポリアミドと塩化ビニル樹脂とを含有する特定の樹脂組成物(以下、本組成物ということがある。)よりなる。 The insulator is made of a specific resin composition (hereinafter sometimes referred to as the present composition) containing a plant-derived polyamide and a vinyl chloride resin.
植物由来のポリアミドは、例えばトウゴマから採取されるひまし油を原料とすることができる。このひまし油からは、11−アミノウンデカン酸を合成することができる。得られた11−アミノウンデカン酸を重合することにより、植物由来のポリアミドを得ることができる。 The plant-derived polyamide can be made from, for example, castor oil collected from castor bean. From this castor oil, 11-aminoundecanoic acid can be synthesized. Plant-derived polyamide can be obtained by polymerizing the obtained 11-aminoundecanoic acid.
植物由来のポリアミドは、原油由来のものではないため、カーボンニュートラルの観点から、二酸化炭素の増加を抑えるものである。植物由来のポリアミドは、植物由来のものではあるが、生分解性がない。このため、生分解性の他のバイオマスプラスチックと比べて、耐久性に優れる。また、耐水性にも優れる。 Since plant-derived polyamide is not derived from crude oil, it suppresses the increase in carbon dioxide from the viewpoint of carbon neutrality. Plant-derived polyamides are plant-derived, but are not biodegradable. For this reason, it is excellent in durability compared with other biodegradable biomass plastics. Moreover, it is excellent also in water resistance.
植物由来のポリアミドとしては、具体的には、例えばアルケマ社のBESV O FDA、BESN O P40 TL、BESN O P20 TL、BESN O TL、BECN O TL、BMN O TLDなどを挙げることができる。これらは単独で用いることもできるし、2つ以上を組み合わせて用いることもできる。 Specific examples of the plant-derived polyamide include BESV O FDA, BESN O P40 TL, BESN O P20 TL, BESN O TL, BECN O TL, and BMN O TLD from Arkema. These can be used alone or in combination of two or more.
植物由来のポリアミドは、ASTM D1238に準拠して測定される230℃、21.18Nにおけるメルトフローレイトが0.1〜50g/10分の範囲内であることが好ましい。植物由来のポリアミドのメルトフローレイトが特定の範囲内であると、ともに用いる塩化ビニル樹脂との相溶性が高くなるため、耐寒性を低下させにくくできる。この観点から、より好ましくは0.2〜45g/10分の範囲内、さらに好ましくは0.3〜40g/10分の範囲内である。 The plant-derived polyamide preferably has a melt flow rate at 230 ° C. and 21.18 N measured in accordance with ASTM D1238 in the range of 0.1 to 50 g / 10 minutes. When the melt flow rate of the plant-derived polyamide is within a specific range, the compatibility with the vinyl chloride resin used together increases, so that the cold resistance can be hardly lowered. From this viewpoint, it is more preferably in the range of 0.2 to 45 g / 10 minutes, and still more preferably in the range of 0.3 to 40 g / 10 minutes.
例示する植物由来のポリアミドのメルトフローレイトは、次の通りである。すなわち、BESV O FDA:0.5g/10分、BESN O P40 TL:0.1g/10分、BESN O P20 TL:0.05g/10分、BESN O TL:1.0g/10分、BECN O TL:30g/10分、BMN O TLD:55g/10分である。 The melt flow rate of the plant-derived polyamide exemplified is as follows. That is, BESV O FDA: 0.5 g / 10 min, BESN O P40 TL: 0.1 g / 10 min, BESN O P20 TL: 0.05 g / 10 min, BESN O TL: 1.0 g / 10 min, BECN O TL: 30 g / 10 min, BMN O TLD: 55 g / 10 min.
植物由来のポリアミドの含有量は、特に限定されるものではないが、本組成物の樹脂成分中における割合として、10〜50質量%程度であれば良い。本組成物は、植物由来のポリアミドを含有するため、環境負荷の低減に貢献できる。なお、植物由来のポリアミドの含有量が本組成物の樹脂成分中における割合として50質量%を超える場合において、植物由来のポリアミドのメルトフローレイトが0.1g/10分未満あるいは50g/10分超となると、耐寒性が低下しやすい傾向にある。 The content of the plant-derived polyamide is not particularly limited, but may be about 10 to 50% by mass as a ratio in the resin component of the composition. Since this composition contains plant-derived polyamide, it can contribute to reduction of an environmental burden. When the content of the plant-derived polyamide exceeds 50% by mass in the resin component of the composition, the plant-derived polyamide has a melt flow rate of less than 0.1 g / 10 minutes or more than 50 g / 10 minutes. Then, the cold resistance tends to decrease.
植物由来のポリアミドとともに用いる塩化ビニル樹脂は、市販のものを用いることができる。このようなものとしては、昭和電工社製「エラスレン」シリーズや、大洋塩ビ社製「リューロン」シリーズなどを挙げることができる。これらは単独で用いても良いし、2種以上を組み合わせて用いても良い。 A commercially available thing can be used for the vinyl chloride resin used with plant-derived polyamide. As such a thing, the "Eraslen" series made by Showa Denko KK, the "Luron" series made by Taiyo PVC, etc. can be mentioned. These may be used alone or in combination of two or more.
塩化ビニル樹脂は、可塑剤を含有していても良い。可塑剤としてはジメチルフタレート(DMP)、ジエチルフタレート(DEP)、ジブチルフタレート(DBP)、ジイソデシルフタレート(DINP)、ジ−2−エチルヘキシルフタレート(DOP)などを挙げることができる。 The vinyl chloride resin may contain a plasticizer. Examples of the plasticizer include dimethyl phthalate (DMP), diethyl phthalate (DEP), dibutyl phthalate (DBP), diisodecyl phthalate (DINP), and di-2-ethylhexyl phthalate (DOP).
本組成物は塩化ビニル樹脂を含有することから、耐水性の低下を抑えることができるとともに、難燃性も良好である。このため、難燃剤を配合しなくても、自動車等の車両に用いられる絶縁電線として求められる難燃性を十分に確保することができる場合がある。あるいは、難燃剤の配合量を極力減らすことができる。したがって、難燃剤の配合によるコストの上昇を抑えることができる。 Since this composition contains a vinyl chloride resin, it can suppress a decrease in water resistance and also has good flame retardancy. For this reason, even if it does not mix | blend a flame retardant, the flame retardance calculated | required as an insulated wire used for vehicles, such as a motor vehicle, can fully be ensured. Or the compounding quantity of a flame retardant can be reduced as much as possible. Therefore, an increase in cost due to the blending of the flame retardant can be suppressed.
このような難燃性を確保する観点から、塩化ビニル樹脂の含有量は、本組成物の樹脂成分中における割合として、10質量%以上であることが好ましい。より好ましくは15質量%以上、さらに好ましくは20質量%以上である。一方、塩化ビニル樹脂の含有量の上限値としては、特に限定されるものではないが、再生可能なバイオマス資源を用いて環境負荷の低減を図る観点から、本組成物の樹脂成分中における割合として、90質量%以下であることが好ましい。より好ましくは85質量%以下である。 From the viewpoint of ensuring such flame retardancy, the content of the vinyl chloride resin is preferably 10% by mass or more as a ratio in the resin component of the present composition. More preferably, it is 15 mass% or more, More preferably, it is 20 mass% or more. On the other hand, the upper limit of the content of the vinyl chloride resin is not particularly limited, but from the viewpoint of reducing the environmental burden using renewable biomass resources, the ratio in the resin component of the composition 90% by mass or less is preferable. More preferably, it is 85 mass% or less.
本組成物中には、上記樹脂成分以外に、物性を損なわない範囲で、必要に応じて、他の樹脂成分を含有していても良い。他の樹脂成分としては、他のオレフィン系樹脂を挙げることができる。他のオレフィン系樹脂としては、原油由来のものを挙げることができる。このような他のオレフィン系樹脂を含む場合にも、耐水性の低下は抑えられる。 In the present composition, in addition to the above resin components, other resin components may be contained as necessary within a range not impairing the physical properties. Examples of other resin components include other olefin resins. Examples of other olefinic resins include those derived from crude oil. Even when such other olefin-based resins are included, a decrease in water resistance can be suppressed.
他のオレフィン系樹脂としては、ポリエチレン、ポリプロピレン等のポリオレフィンや、エチレン−ビニル酢酸共重合体(EVA)、エチレン−アクリル酸エチル共重合体(EEA)等のエチレン共重合体、プロピレン−ビニル酢酸共重合体、プロピレン−アクリル酸エチル共重合体等のプロピレン共重合体などを挙げることができる。ポリエチレンとしては、低密度ポリエチレン、高密度ポリエチレン、直鎖状低密度ポリエチレン、メタロセンポリエチレンなどを挙げることができる。ポリプロピレンとしては、ホモポリプロピレン、ブロックポリプロピレン、ランダムポリプロピレンなどを挙げることができる。他のオレフィン系樹脂は、酸無水物やカルボン酸等により変性されていても良いし、変性されていなくても良い。 Other olefin-based resins include polyolefins such as polyethylene and polypropylene, ethylene copolymers such as ethylene-vinyl acetate copolymer (EVA) and ethylene-ethyl acrylate copolymer (EEA), and propylene-vinyl acetate copolymer. Examples thereof include a polymer and a propylene copolymer such as a propylene-ethyl acrylate copolymer. Examples of polyethylene include low density polyethylene, high density polyethylene, linear low density polyethylene, and metallocene polyethylene. Examples of polypropylene include homopolypropylene, block polypropylene, and random polypropylene. Other olefin-based resins may be modified with an acid anhydride or carboxylic acid, or may not be modified.
他のオレフィン系樹脂としては、耐摩耗性に優れる組成物が得られるなどの観点から、ポリプロピレンである。特に好ましくは、耐寒性と耐摩耗性とのバランスに優れる組成物が得られるなどの観点から、ポリプロピレンのうちでも、ポリエチレンとのブロック共重合体(ブロックポリプロピレン)である。 Another olefin-based resin is polypropylene from the viewpoint of obtaining a composition having excellent wear resistance. Particularly preferable is a block copolymer with polyethylene (block polypropylene) from the viewpoint of obtaining a composition having an excellent balance between cold resistance and wear resistance.
本組成物中には、上記成分以外に、物性を損なわない範囲で、必要に応じて、添加剤を適宜配合することができる。添加剤としては、例えば、難燃剤、酸化防止剤、銅害防止剤(金属不活性化剤)、紫外線吸収剤、紫外線隠蔽剤、加工助剤(ワックスなど)、顔料、相溶化剤、可塑剤などを挙げることができる。 In the present composition, in addition to the above components, additives can be appropriately blended as necessary within a range not impairing physical properties. Examples of additives include flame retardants, antioxidants, copper damage inhibitors (metal deactivators), UV absorbers, UV masking agents, processing aids (such as waxes), pigments, compatibilizers, and plasticizers. And so on.
本組成物の添加剤として配合可能な難燃剤としては、特に限定されるものではない。例えば、水酸化マグネシウム、水酸化アルミニウムなどの金属水和物、メラミンイソシアヌレートなどの窒素系難燃剤、エチレンビス(テトラブロモベンゼン)、エチレンビス(ペンタブロモベンゼン)などのハロゲン系難燃剤などを挙げることができる。これらの難燃剤の配合量は、適宜定めることができる。 The flame retardant that can be blended as an additive of the present composition is not particularly limited. For example, metal hydrates such as magnesium hydroxide and aluminum hydroxide, nitrogen flame retardants such as melamine isocyanurate, halogen flame retardants such as ethylene bis (tetrabromobenzene) and ethylene bis (pentabromobenzene), etc. be able to. The amount of these flame retardants can be determined as appropriate.
本発明に係る絶縁電線は、例えば、導体の外周に本組成物を押出成形するなどして製造することができる。本組成物の調製方法は、特に限定されるものではなく、公知の方法を用いることができる。例えば、本組成物の必須成分および任意添加成分をバンバリミキサー、加圧ニーダー、混練押出機、二軸混練押出機、ロール等の通常の混練機で溶融混練して均一に分散することで、本組成物を調製することができる。 The insulated wire according to the present invention can be produced, for example, by extruding the composition on the outer periphery of a conductor. The preparation method of this composition is not specifically limited, A well-known method can be used. For example, the essential components and optional additional components of the present composition are melt-kneaded and uniformly dispersed in a conventional kneader such as a Banbury mixer, a pressure kneader, a kneading extruder, a twin-screw kneading extruder, and a roll. A composition can be prepared.
以上の構成の本発明に係る絶縁電線においては、絶縁体を構成する材料にバイオマス資源から得られるポリアミドを用いているため、従来の絶縁電線と比較して、化石資源の使用量を低減できる。また、バイオマス資源は、化石資源と比較して、比較的短期に再生可能な資源であり、カーボンニュートラルな性質を有する。したがって、本発明に係る絶縁電線によれば、従来よりも環境負荷の低減を図ることができる。 In the insulated wire according to the present invention having the above-described configuration, since the polyamide obtained from biomass resources is used as the material constituting the insulator, the amount of fossil resources used can be reduced compared to conventional insulated wires. Biomass resources are resources that can be regenerated in a relatively short period of time compared to fossil resources, and have carbon neutral properties. Therefore, according to the insulated wire which concerns on this invention, reduction of an environmental load can be aimed at rather than before.
また、本発明においては、バイオマス資源から得られるポリアミド自体が耐水性を有するものであるため、絶縁体を構成する材料にバイオマス資源を用いたときにも、絶縁体の耐水性を低下させないようにすることができる。併せて、絶縁体を構成する材料に塩化ビニル樹脂を用いているため、絶縁体の耐水性を低下させず、優れた耐水性を示す。 Further, in the present invention, since the polyamide itself obtained from biomass resources has water resistance, even when biomass resources are used as a material constituting the insulator, the water resistance of the insulator is not lowered. can do. In addition, since a vinyl chloride resin is used as a material constituting the insulator, the water resistance of the insulator is not lowered and excellent water resistance is exhibited.
以下に本発明を実施例により具体的に説明するが、本発明はこれらによって限定されるものではない。 EXAMPLES The present invention will be specifically described below with reference to examples, but the present invention is not limited thereto.
(実施例1〜11)
表1に記載の成分組成(質量部)となるように、植物由来のポリアミド成分、塩化ビニル樹脂成分、添加剤を加え、二軸混練機を用いて200℃で混合した後、ペレタイザーにてペレット状に成形して樹脂組成物のペレットを得た。このペレットを押出成形機により、軟銅線を7本撚り合わせた軟銅撚線の導体(断面積:0.5mm2)の外周に0.2mm厚で押出して、樹脂組成物からなる絶縁体により導体が被覆された実施例1〜11に係る絶縁電線を得た。
(Examples 1 to 11)
After adding a plant-derived polyamide component, a vinyl chloride resin component, and additives so as to have the component composition (parts by mass) shown in Table 1, the mixture is mixed at 200 ° C. using a twin-screw kneader, and then pelletized by a pelletizer. The resin composition pellets were obtained. The pellets were extruded by an extruder at a thickness of 0.2 mm onto the outer periphery of a annealed copper stranded wire conductor (cross-sectional area: 0.5 mm 2 ) in which seven annealed copper wires were twisted together, and the conductor was formed by an insulator made of a resin composition. The insulated wire which concerns on Examples 1-11 with which was covered was obtained.
(比較例1〜7)
表2に記載の他のバイオマスプラスチックと添加剤を用いて絶縁体の組成物を形成し、実施例と同様にして、比較例1〜7に係る絶縁電線を得た。
(Comparative Examples 1-7)
The composition of the insulator was formed using other biomass plastics and additives described in Table 2, and the insulated wires according to Comparative Examples 1 to 7 were obtained in the same manner as in the Examples.
実施例及び比較例で得られた絶縁電線を用いて、耐寒性試験及び耐水性試験を行った。試験の結果を表1〜2に示す。耐寒性試験方法及び耐水性試験方法は下記の通りである。 Using the insulated wires obtained in Examples and Comparative Examples, a cold resistance test and a water resistance test were performed. The test results are shown in Tables 1-2. The cold resistance test method and the water resistance test method are as follows.
〔耐寒性試験方法〕
JIS C3005に準拠して行った。すなわち、実施例、比較例の絶縁電線を38mmの長さに切断し試験片とし、試験片を耐寒性試験機に装着し、所定の温度まで冷却し、打撃具で打撃して、試験片の打撃後の状態を観察した。5本の試験片を用いて、5本の試験片が全て割れた温度を耐寒温度とした。
[Cold resistance test method]
This was performed in accordance with JIS C3005. That is, the insulated wires of Examples and Comparative Examples were cut into 38 mm lengths to make test pieces, the test pieces were mounted on a cold resistance tester, cooled to a predetermined temperature, hit with a hitting tool, The condition after hitting was observed. Using five test pieces, the temperature at which all five test pieces were broken was defined as the cold resistant temperature.
〔耐水性試験方法〕
ISO6722に準拠して、実施例、比較例の絶縁電線を80℃の温水に5週間浸漬した後、絶縁体の絶縁抵抗値を測定した。絶縁抵抗値が1×109Ω・mm以上であったものを合格「○」とし、絶縁抵抗値が1×109Ω・mm未満であったものを不合格「×」とした。
[Water resistance test method]
In accordance with ISO 6722, the insulated wires of Examples and Comparative Examples were immersed in warm water at 80 ° C. for 5 weeks, and then the insulation resistance value of the insulator was measured. A sample having an insulation resistance value of 1 × 10 9 Ω · mm or more was evaluated as “good”, and a sample having an insulation resistance value of less than 1 × 10 9 Ω · mm was determined as “failed”.
(植物由来のポリアミド成分)
いずれもアルケマ社製
・BESV O FDA:0.5g/10分
・BESN O P40 TL:0.1g/10分
・BESN O P20 TL:0.05g/10分
・BESN O TL:1.0g/10分
・BMN O TLD:55g/10分
・BECN O TL:30g/10分
(Plant-derived polyamide component)
All are made by Arkema, Inc. · BESV O FDA: 0.5 g / 10 min · BESN O P40 TL: 0.1 g / 10 min · BESN O P20 TL: 0.05 g / 10 min · BESN O TL: 1.0 g / 10 Minutes · BMN O TLD: 55 g / 10 minutes · BECN O TL: 30 g / 10 minutes
(塩化ビニル樹脂成分)
・エラスレン301A、303B:昭和電工社製
・リューロンE−1700、E−2200:大洋塩ビ社製
(Vinyl chloride resin component)
・ Elasticene 301A, 303B: Showa Denko ・ Luron E-1700, E-2200: Taiyo PVC
(他のバイオマスプラスチック成分)
・ポリ乳酸(V351X51):東レ社製
・ポリ乳酸(V554R10):東レ社製
・ポリ乳酸(TCA8070MN):ユニチカ社製
・酢酸セルロース(15300−26):ダイセル社製
・酢酸セルロース(15300−31):ダイセル社製
・ポリブチレンスクシネート(NF01U):ケミテック社製
・ポリブチレンスクシネート(ビオノーレ1020):昭和高分子社製
(Other biomass plastic components)
・ Polylactic acid (V351X51): manufactured by Toray Industries, Inc. ・ Polylactic acid (V554R10): manufactured by Toray Industries, Inc. ・ Polylactic acid (TCA8070MN): manufactured by Unitika ・ Cellulose acetate (15300-26): manufactured by Daicel Corporation ・ Cellulose acetate (15300-31) : Manufactured by Daicel, Inc./polybutylene succinate (NF01U): manufactured by Chemtech, Inc./polybutylene succinate (Bionore 1020): manufactured by Showa Polymer Co., Ltd.
(添加剤成分)
・酸化防止剤(イルガノックス1010):チバスペシャリティケミカルズ社製
(Additive component)
Antioxidant (Irganox 1010): manufactured by Ciba Specialty Chemicals
比較例は、樹脂成分が、ポリ乳酸、酢酸セルロース、ポリブチレンスクシネートからなるバイオマスプラスチック成分のみからなるものであるため、耐水性に劣っている。これに対し、実施例は、樹脂成分が、植物由来のポリアミド成分と塩化ビニル樹脂成分とを含有するものからなるため、耐寒性を維持しつつ、耐水性にも優れることが分かる。 The comparative example is inferior in water resistance because the resin component consists only of a biomass plastic component composed of polylactic acid, cellulose acetate, and polybutylene succinate. On the other hand, since the resin component consists of a plant-derived polyamide component and a vinyl chloride resin component, it can be seen that the examples are excellent in water resistance while maintaining cold resistance.
したがって、本発明に係る絶縁電線によれば、再生可能なバイオマス資源を用いて環境負荷の低減を図ることができるとともに、この場合においても耐水性に優れる絶縁電線が得られることが確認できた。 Therefore, according to the insulated wire which concerns on this invention, while being able to aim at reduction of an environmental load using the renewable biomass resource, it has confirmed that the insulated wire excellent in water resistance was obtained also in this case.
以上、本発明の実施の形態について詳細に説明したが、本発明は上記実施の形態に何ら限定されるものではなく、本発明の要旨を逸脱しない範囲で種々の改変が可能である。 Although the embodiments of the present invention have been described in detail above, the present invention is not limited to the above-described embodiments, and various modifications can be made without departing from the gist of the present invention.
Claims (3)
前記絶縁体が、植物由来のポリアミドと塩化ビニル樹脂とを含有する樹脂組成物よりなることを特徴とする絶縁電線。 In an insulated wire comprising a conductor and an insulator covering the outer periphery of the conductor,
The insulated wire is characterized in that the insulator is made of a resin composition containing a plant-derived polyamide and a vinyl chloride resin.
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012227101A (en) * | 2011-04-22 | 2012-11-15 | Yazaki Corp | Insulating composition and electric wire and cable |
| CN103554775A (en) * | 2013-10-31 | 2014-02-05 | 合肥得润电子器件有限公司 | Modified polyvinyl chloride insulation material for automobile wire harness |
-
2011
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012227101A (en) * | 2011-04-22 | 2012-11-15 | Yazaki Corp | Insulating composition and electric wire and cable |
| CN103554775A (en) * | 2013-10-31 | 2014-02-05 | 合肥得润电子器件有限公司 | Modified polyvinyl chloride insulation material for automobile wire harness |
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