JPS62236826A - Coated metal wire - Google Patents
Coated metal wireInfo
- Publication number
- JPS62236826A JPS62236826A JP7943886A JP7943886A JPS62236826A JP S62236826 A JPS62236826 A JP S62236826A JP 7943886 A JP7943886 A JP 7943886A JP 7943886 A JP7943886 A JP 7943886A JP S62236826 A JPS62236826 A JP S62236826A
- Authority
- JP
- Japan
- Prior art keywords
- polyamide
- component
- metal wire
- coated metal
- wire
- 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
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 19
- 239000002184 metal Substances 0.000 title claims abstract description 19
- 239000004952 Polyamide Substances 0.000 claims abstract description 30
- 229920002647 polyamide Polymers 0.000 claims abstract description 30
- 230000033001 locomotion Effects 0.000 claims abstract description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 12
- PBLZLIFKVPJDCO-UHFFFAOYSA-N 12-aminododecanoic acid Chemical compound NCCCCCCCCCCCC(O)=O PBLZLIFKVPJDCO-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229920000151 polyglycol Polymers 0.000 claims abstract description 10
- 239000010695 polyglycol Substances 0.000 claims abstract description 10
- -1 polytetramethylene Polymers 0.000 claims abstract description 10
- 230000005540 biological transmission Effects 0.000 claims abstract description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims abstract description 6
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 claims abstract description 4
- GUOSQNAUYHMCRU-UHFFFAOYSA-N 11-Aminoundecanoic acid Chemical compound NCCCCCCCCCCC(O)=O GUOSQNAUYHMCRU-UHFFFAOYSA-N 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 abstract description 4
- 239000011248 coating agent Substances 0.000 abstract description 3
- 238000000576 coating method Methods 0.000 abstract description 3
- 239000000178 monomer Substances 0.000 abstract description 3
- 238000005299 abrasion Methods 0.000 abstract description 2
- 239000004014 plasticizer Substances 0.000 description 5
- TVIDDXQYHWJXFK-UHFFFAOYSA-N dodecanedioic acid Chemical compound OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- UFFRSDWQMJYQNE-UHFFFAOYSA-N 6-azaniumylhexylazanium;hexanedioate Chemical class [NH3+]CCCCCC[NH3+].[O-]C(=O)CCCCC([O-])=O UFFRSDWQMJYQNE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexamethylene diamine Natural products NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は被覆された金属線に関し、更に詳細には一定方
向の動ぎ、回転動、往復動等の運動を伝達する用に供さ
れる被覆された金属線に関する。Detailed Description of the Invention (Industrial Application Field) The present invention relates to a coated metal wire, and more specifically, it is used for transmitting motion such as motion in a fixed direction, rotational motion, reciprocating motion, etc. Concerning coated metal wire.
(従来技術および問題点)
索導管の内索、車への回転伝達用ワイヤー等、金属線は
各種の運動を伝達する目的で広く用いられている。これ
らの金属線には摩擦摩耗特性を向上させ金属線を保護す
る目的で、広く熱可塑性樹脂が被覆されている。熱可塑
性樹脂としては一般にポリエチレン、ポリプロピレン、
ポリアミド等が用いられるが、特に摩擦摩耗特性、耐熱
性が要求される場合はポリアミドが好んで用いられる。(Prior Art and Problems) Metal wires are widely used for the purpose of transmitting various motions, such as inner cables of cable conduits and wires for transmitting rotation to cars. These metal wires are widely coated with thermoplastic resin for the purpose of improving friction and wear characteristics and protecting the metal wires. Thermoplastic resins generally include polyethylene, polypropylene,
Polyamide and the like are used, and polyamide is preferably used especially when friction and wear characteristics and heat resistance are required.
しかしながら、ポリアミドは摩擦摩耗特性、強度、耐熱
性に優れる反面、本質的に硬い樹脂であるため金属線の
しなやかさを損い、このため運動、力の伝達に円滑さを
欠くことがある。また低温で用いられた時、ポリアミド
の脆化によって被覆に割れが生じる場合がある。However, although polyamide has excellent friction and wear characteristics, strength, and heat resistance, it is essentially a hard resin, which impairs the flexibility of metal wires, which may result in a lack of smooth movement and force transmission. Furthermore, when used at low temperatures, the coating may crack due to brittleness of the polyamide.
これらの欠点を改善するため、ポリアミドを柔軟にする
目的で1)可塑剤を添加する2)ポリアミドとゴム成分
をブレンドする等の方法がとられてきた。しかしながら
、可塑剤を添加したものは、使用中可塑剤の揮発、抽出
等によって硬化してくる欠点があると共に、低温では可
塑剤の凍結による逆可塑化現象により柔軟性が失われる
。In order to improve these drawbacks, methods such as 1) adding a plasticizer and 2) blending the polyamide and a rubber component have been taken in order to make the polyamide flexible. However, those to which a plasticizer is added have the disadvantage that they harden during use due to volatilization, extraction, etc. of the plasticizer, and at low temperatures they lose flexibility due to reverse plasticization due to freezing of the plasticizer.
ゴム等のブレンドは摩擦摩耗特性が大幅に低ドする欠点
がある。Blends of rubber, etc. have the disadvantage of significantly lower friction and wear characteristics.
本発明の目的はしなやかであり、低温で割れが生じず、
かつ摩擦摩耗特性、耐熱性に優れた運動伝達用被覆金属
線を提供することにある。The purpose of the present invention is to be flexible, not crack at low temperatures,
Another object of the present invention is to provide a coated metal wire for motion transmission that has excellent friction and wear characteristics and heat resistance.
(問題点を解決するだめの手段)
本発明は分子中にポリアミド成分およびポリグリコール
成分を有するポリアミド共重合体により被覆された運動
伝達用被覆金属線である。(Means for Solving the Problems) The present invention is a coated metal wire for motion transmission coated with a polyamide copolymer having a polyamide component and a polyglycol component in the molecule.
本発明におけるポリアミド成分とは、ポリアミド形成性
モノマーから重合された低重合度の単−重合体又は共重
合体である。ポリアミド形成性モノマーとしてはカプロ
ラクタム、ラウリルラクタム等のラクタム、12−アミ
ノドデカン酸、11−アミノウンデカン酸等のω−アミ
ノカルボン酸、アジピン酸へキサメチレンジアミン塩、
ドデカンニ酸へキサメチレンジアミン塩、イソフタル酸
イソボロンジアミン塩等のジカルボン酸とジアミンの塩
が例示される。なかでもポリアミド成分がラウリルラク
タム、12−アミノドデカン酸、11−アミノウンデカ
ン酸から重合されたポリアミドである場合は、吸水によ
る物性の変化が小さく、最も好ましい被覆金属線が得ら
れる。The polyamide component in the present invention is a low degree of polymerization monopolymer or copolymer polymerized from polyamide-forming monomers. Examples of polyamide-forming monomers include lactams such as caprolactam and lauryllactam, ω-aminocarboxylic acids such as 12-aminododecanoic acid and 11-aminoundecanoic acid, adipic acid hexamethylene diamine salt,
Examples include salts of dicarboxylic acids and diamines such as hexamethylene diamine dodecanoic acid salt and isophthalic acid isoborone diamine salt. Among these, when the polyamide component is a polyamide polymerized from lauryllactam, 12-aminododecanoic acid, and 11-aminoundecanoic acid, the most preferable coated metal wire can be obtained since the change in physical properties due to water absorption is small.
ポリアミド成分の量は、30〜95重量部が好ましく用
いられる。ポリアミド成分の量が95重は部を越えると
柔軟性が充分でなく、従って被覆金属線のしなやかさが
充分でない。ポリアミド成分が30重量部以下であると
摩擦摩耗特性、耐熱性、機械的強度が低下し、従ってポ
リアミドを被覆した金属線の特徴が得られない。The amount of polyamide component used is preferably 30 to 95 parts by weight. If the amount of the polyamide component exceeds 95 parts by weight, the flexibility will not be sufficient, and therefore the coated metal wire will not have sufficient flexibility. If the polyamide component is less than 30 parts by weight, the friction and wear properties, heat resistance, and mechanical strength will be reduced, and therefore the characteristics of the metal wire coated with polyamide cannot be obtained.
ポリグリコール成分としては、ポリエチレングリコール
、ポリプロピレングリコール、ボリテl〜ラメチレング
リコールが例示できる。水および熱に対する安定性から
ポリテトラメチレングリコールが最も好ましく用いられ
、その平均分子量が300〜2200のものが更に好ま
しく用いられる。Examples of the polyglycol component include polyethylene glycol, polypropylene glycol, and ramethylene glycol. Polytetramethylene glycol is most preferably used because of its stability against water and heat, and those having an average molecular weight of 300 to 2,200 are even more preferably used.
ポリアミド成分とポリグリコール成分を化学結合する手
段はいかなる方法をとってもよいが、たとえばアジピン
酸、ドデカンニ酸等のジカルボン酸をポリグリコールと
ほぼ等モル重合時に加えることにより両者をエステル結
合で結合する方法、あるいはポリグリコールの両末端を
アミン化しポリアミドの両末端をカルボキシル基として
アミド結合で結合する方法が例示できる。具体的には、
たとえば12−アミノドデカン酸とα、ω−ジヒドロキ
シポリテトラメチレングリコールと、α、ω−ジヒドロ
キシポリテトラメチレングリコールと等モルのドデカン
ニ酸を攪拌しながら、窒素気流中で240℃に2時間加
熱して発生ずる縮合水を除き、その後5m1lllIO
の減圧下に更に5時間線合を進めることによって重合す
ることができる。Any method may be used to chemically bond the polyamide component and the polyglycol component; for example, a method in which a dicarboxylic acid such as adipic acid or dodecanedioic acid is added during polymerization in substantially equimolar amounts with the polyglycol to bond the two through an ester bond; Alternatively, a method can be exemplified in which both ends of polyglycol are aminated and both ends of polyamide are connected as carboxyl groups with amide bonds. in particular,
For example, 12-aminododecanoic acid, α, ω-dihydroxy polytetramethylene glycol, and α, ω-dihydroxy polytetramethylene glycol and equimolar amounts of dodecanedioic acid are heated to 240°C for 2 hours in a nitrogen stream while stirring. Remove the generated condensation water, then 5 ml IO
Polymerization can be carried out by further proceeding the linearization for 5 hours under reduced pressure.
本発明の被覆材には染顔料、各種安定剤、可塑剤、充填
剤、油等を添加することができる。たとえばポリテトラ
フルオロエチレン粉末、グラファイト、二硫化モリブデ
ン、シリコンオイル等を添加できる。Dyes and pigments, various stabilizers, plasticizers, fillers, oils, etc. can be added to the coating material of the present invention. For example, polytetrafluoroethylene powder, graphite, molybdenum disulfide, silicone oil, etc. can be added.
本発明に用いられる金属線は、単線であっても良いし二
本以上の撚線であっても良い。The metal wire used in the present invention may be a single wire or two or more twisted wires.
(発明の効果)
本発明による被覆金属線は、しなやかでかつ摩m摩耗特
性に優れているため、たとえば自動車に用いられる索導
管の内索、プリンター等のoAll器の動力伝達機構に
好ましく用いられ得る。(Effects of the Invention) The coated metal wire according to the present invention is flexible and has excellent abrasion characteristics, so it is preferably used, for example, in the inner cable of a cable conduit used in an automobile, or in the power transmission mechanism of an oAll device such as a printer. obtain.
(実施例) 以下に実施例により本発明をさらに詳しく説明する。(Example) The present invention will be explained in more detail with reference to Examples below.
実施例1〜3、比較例1〜2
0.11φ鋼線を10本撚った線に、押出成形により表
−1に示す樹脂を約0.2mm厚みに被覆した。Examples 1 to 3, Comparative Examples 1 to 2 Ten twisted 0.11φ steel wires were coated with the resin shown in Table 1 to a thickness of about 0.2 mm by extrusion molding.
これを第1図のように、モーターの動力を別の車に伝え
るワイヤーとして用いた場合のモーターの消費電流を測
定し、その結果を表−1に示す。When this wire was used as a wire to transmit the power of the motor to another car as shown in Figure 1, the current consumption of the motor was measured, and the results are shown in Table 1.
またこのワイヤーを80℃において1ケ月熱老化した後
、同様の試験を行った結果を表−1に示す。Table 1 shows the results of a similar test conducted after heat aging this wire at 80° C. for one month.
本発明のワイヤーがしなやかであり、動力伝達が容易で
あることがわかる。It can be seen that the wire of the present invention is flexible and can easily transmit power.
第1図は実施例1〜3および比較例1〜2の試験方法を
示す説明図である。第2図は実施例4〜6、比較例3〜
4の試験方法を示す説明図である。
1・・・モーターにつながった車、2.3・・・車、4
・・・ワイヤー、5・・・ワイヤー固定部、6・・・外
管、7・・・内索FIG. 1 is an explanatory diagram showing the test method of Examples 1 to 3 and Comparative Examples 1 to 2. Figure 2 shows Examples 4 to 6 and Comparative Examples 3 to 6.
FIG. 4 is an explanatory diagram showing test method No. 4. 1...Car connected to a motor, 2.3...Car, 4
...Wire, 5...Wire fixing part, 6...Outer tube, 7...Inner cable
Claims (1)
を有するポリアミド共重合体により被覆された運動伝達
用被覆金属線。 2 ポリアミド成分が12−アミノドデカン酸、ラウリ
ルラクタム又は11−アミノウンデカン酸から重合され
たポリアミドであり、ポリグール成分がポリテトラメチ
レングリコールである特許請求の範囲第1項記載の被覆
金属線。 3 ポリアミド成分が30〜95重量部、ポリグリコー
ル成分が70〜5重量部である特許請求の範囲第1項又
は第2項記載の被覆金属線。[Scope of Claims] 1. A coated metal wire for motion transmission coated with a polyamide copolymer having a polyamide component and a polyglycol component in the molecule. 2. The coated metal wire according to claim 1, wherein the polyamide component is a polyamide polymerized from 12-aminododecanoic acid, lauryllactam or 11-aminoundecanoic acid, and the polygol component is polytetramethylene glycol. 3. The coated metal wire according to claim 1 or 2, wherein the polyamide component is 30 to 95 parts by weight and the polyglycol component is 70 to 5 parts by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61079438A JPH0715004B2 (en) | 1986-04-07 | 1986-04-07 | Coated metal wire for motion transmission |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61079438A JPH0715004B2 (en) | 1986-04-07 | 1986-04-07 | Coated metal wire for motion transmission |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62236826A true JPS62236826A (en) | 1987-10-16 |
JPH0715004B2 JPH0715004B2 (en) | 1995-02-22 |
Family
ID=13689881
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61079438A Expired - Lifetime JPH0715004B2 (en) | 1986-04-07 | 1986-04-07 | Coated metal wire for motion transmission |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0715004B2 (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS608518A (en) * | 1983-06-09 | 1985-01-17 | ハツク、マニユフアクチユアリング、カンパニ− | Anchoring tool and production thereof |
-
1986
- 1986-04-07 JP JP61079438A patent/JPH0715004B2/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS608518A (en) * | 1983-06-09 | 1985-01-17 | ハツク、マニユフアクチユアリング、カンパニ− | Anchoring tool and production thereof |
Also Published As
Publication number | Publication date |
---|---|
JPH0715004B2 (en) | 1995-02-22 |
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