JPH0350822B2 - - Google Patents
Info
- Publication number
- JPH0350822B2 JPH0350822B2 JP6593084A JP6593084A JPH0350822B2 JP H0350822 B2 JPH0350822 B2 JP H0350822B2 JP 6593084 A JP6593084 A JP 6593084A JP 6593084 A JP6593084 A JP 6593084A JP H0350822 B2 JPH0350822 B2 JP H0350822B2
- Authority
- JP
- Japan
- Prior art keywords
- tin
- fusible
- alloy
- brass
- fusing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000004020 conductor Substances 0.000 claims description 18
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 17
- 229910045601 alloy Inorganic materials 0.000 claims description 15
- 239000000956 alloy Substances 0.000 claims description 15
- 229910001369 Brass Inorganic materials 0.000 claims description 7
- 239000010951 brass Substances 0.000 claims description 7
- 230000008018 melting Effects 0.000 description 7
- 238000002844 melting Methods 0.000 description 7
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 6
- 239000011701 zinc Substances 0.000 description 6
- 229910052725 zinc Inorganic materials 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 229910000730 Beta brass Inorganic materials 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 238000005336 cracking Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910017827 Cu—Fe Inorganic materials 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 238000005275 alloying Methods 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
- 238000005266 casting Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 210000000078 claw Anatomy 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000001965 increasing effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 238000005482 strain hardening Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01H—ELECTRIC SWITCHES; RELAYS; SELECTORS; EMERGENCY PROTECTIVE DEVICES
- H01H85/00—Protective devices in which the current flows through a part of fusible material and this current is interrupted by displacement of the fusible material when this current becomes excessive
- H01H85/02—Details
- H01H85/04—Fuses, i.e. expendable parts of the protective device, e.g. cartridges
- H01H85/05—Component parts thereof
- H01H85/055—Fusible members
- H01H85/06—Fusible members characterised by the fusible material
Landscapes
- Fuses (AREA)
Description
【発明の詳細な説明】
本発明はヒユージブルリンクとして好適な可溶
導体用合金に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a fusible conductor alloy suitable for fusible links.
従来、ワイヤハーネスを保護するヒユージブル
リンクの可溶導体としては、主に
() 可溶導体としての軟銅撚線に錫メツキを施
したもの、
() バイメタルに錫をかませたもの(抱合せ)、
() Cu−Fe系合金を用いたもの、
の三種が使用されている。 Conventionally, the fusible conductors of fusible links that protect wire harnesses have mainly been () tin-plated soft copper stranded wire as a fusible conductor, and () tin-plated bimetal (bonded conductor). ), () one using Cu-Fe alloy, and () are used.
このうち、()と()は錫と銅の拡散(融
点降下)を利用して限界電流付近での溶断時間を
速める効果を狙つたものであるが、()〜()
は何れも融点が高い。従つて、溶断限界付近の電
流が流れても温度上昇が緩慢で、溶断までの時間
が長くなる。その結果、可溶導体の赤熱化状態即
ち高温状態が長く続き、これを収容するハウジン
グ等を溶融し、焼損し、通電部が露出して火災を
招く等の危険があつた。 Of these, () and () aim to speed up the fusing time near the limit current by utilizing the diffusion of tin and copper (decreasing the melting point), but () to ()
Both have high melting points. Therefore, even if a current near the fusing limit flows, the temperature rises slowly and it takes a long time until the fusing occurs. As a result, the fusible conductor remains in a red-hot state, that is, a high-temperature state, for a long time, and there is a danger that the housing housing the fusible conductor, etc., may melt and burn out, exposing the current-carrying portion, and causing a fire.
一方、低融点材料という点に着目すれば、亜鉛
やハンダ等の使用も考えられるが、走行、振動す
る自動車等に用いる可溶導体としては、溶断し易
く機械的強度も乏しく不適当である。 On the other hand, if attention is paid to materials with a low melting point, the use of zinc, solder, etc. may be considered, but these materials are unsuitable as they tend to melt and have poor mechanical strength as fusible conductors used in automobiles that run and vibrate.
また、以上のような問題点を解消する材料とし
てはβ黄銅(一般に銅57%、亜鉛43%の合金を示
す。)が注目される。しかし、β黄銅は亜鉛量が
多いため圧延が難しく特に冷間加工では応力腐食
割れ(置割れ)が生じ、また腐食性雰囲気中では
亜鉛が溶出する脱亜鉛現象が起るという問題があ
る。 In addition, β-brass (generally an alloy of 57% copper and 43% zinc) is attracting attention as a material that can solve the above problems. However, β-brass has a large amount of zinc and is therefore difficult to roll, causing stress corrosion cracking (stress cracking) especially during cold working, and dezincing phenomenon in which zinc is eluted in a corrosive atmosphere.
本発明は上記の問題に鑑みてなされたもので、
鋳物、板、棒材等として汎用されている四六黄銅
(亜鉛40%)に錫0.5〜3.0%を添加することによ
り溶断特性(即ち電流感度)及び耐食性に優れ、
しかも加工性良好な可溶導体が得られることを見
出した。 The present invention was made in view of the above problems, and
By adding 0.5 to 3.0% tin to Shiroku brass (40% zinc), which is commonly used for castings, plates, bars, etc., it has excellent fusing characteristics (i.e. current sensitivity) and corrosion resistance.
Moreover, it has been found that a soluble conductor with good workability can be obtained.
本発明の可溶導体用合金は四六黄銅に錫を重量
で0.5〜3.0%添加することにより得られるが、溶
断特性及び加工性の面から0.8〜1.5%とするのが
好ましい。即ち、本発明合金は四六黄銅に錫を添
加することにより相対的に銅量を減らし、βの割
合を増大させるもので、このβ黄銅は470℃付近
で原子配列が変化して電気抵抗が急激に増大する
性質をできるだけ機械的強度を損わずに利用せん
とするものである。この錫の添加量が0.5%より
少ない範囲では融点降下の度合が少なくシヤープ
な溶断時性が得られず、また、3.0%を越えると
機械的強度が減少して振動を伴う走行車等には実
用性が乏しくなる。 The fusible conductor alloy of the present invention can be obtained by adding 0.5 to 3.0% by weight of tin to Shiroku brass, but from the viewpoint of fusing characteristics and workability, the content is preferably 0.8 to 1.5%. In other words, the alloy of the present invention relatively reduces the amount of copper and increases the proportion of β by adding tin to 460°C, and the atomic arrangement of this β-brass changes at around 470°C and the electrical resistance increases. The aim is to utilize the property of rapidly increasing properties without compromising mechanical strength as much as possible. If the amount of tin added is less than 0.5%, the degree of melting point depression will be small and sharp fusing properties will not be obtained, and if it exceeds 3.0%, the mechanical strength will decrease and it will not be suitable for vehicles with vibrations. It becomes less practical.
第1図は本発明合金と従来品の溶断特性を示す
グラフであつて、縦軸は可溶導体の赤熱化状態か
ら溶断までに要した時間(秒)である。図から明
らかなように、従来のCu−Fe系合金(前記)
は軟銅撚線品(前記)よりも溶断時間が速く、
より安全性を増しているが、本発明の錫入り黄銅
では更に赤熱時間が短縮され、優れた溶断特性を
有する。なお、図中の、、等の数値はヒユ
ージブルリンクを収容した熱可塑性合成樹脂製
(ナイロン66+ガラス繊維30%)ハウジングを
各々10個使用したときの溶融個数を示すものであ
る。 FIG. 1 is a graph showing the fusing characteristics of the alloy of the present invention and a conventional product, in which the vertical axis represents the time (seconds) required from the red-hot state of the fusible conductor to the time of fusing. As is clear from the figure, the conventional Cu-Fe alloy (described above)
has a faster fusing time than the annealed copper stranded wire product (above),
In addition to being safer, the tin-containing brass of the present invention also has a shorter glow time and excellent fusing characteristics. In addition, the numerical values such as , , etc. in the figure indicate the number of melted pieces when 10 housings each made of thermoplastic synthetic resin (nylon 66 + glass fiber 30%) containing fusible links are used.
また、本発明合金には耐食性及び機械的性質改
善のため、鉄、マンガン、アルミニウム、ケイ
素、クロム、マンガン等の金属を四六黄銅に対し
1.0以下の範囲で添加することもできる。 In addition, metals such as iron, manganese, aluminum, silicon, chromium, and manganese are added to the alloy of the present invention to improve corrosion resistance and mechanical properties.
It can also be added in a range of 1.0 or less.
第2図は本発明合金をヒユージブルリンクとし
て使用する場合の実施態様を示すものである。即
ち、1はポリアミド樹脂、ポリプロピレン等の熱
可塑性合成樹脂よりなるハウジング、2はそのカ
バーで、ハウジング1内には可溶導体3と雌端子
4とより構成されたヒユージブルリンク5が収容
されるようになつている。 FIG. 2 shows an embodiment in which the alloy of the present invention is used as a fusible link. That is, 1 is a housing made of thermoplastic synthetic resin such as polyamide resin or polypropylene, 2 is a cover thereof, and a fusible link 5 composed of a fusible conductor 3 and a female terminal 4 is accommodated in the housing 1. It is becoming more and more common.
可溶導体3は、前記の如く四六黄銅に錫を添加
した合金よりなる板状の可溶導体部3aの一端を
雌端子4に圧着等により接続し、他端に連成され
た折曲片部3bに爪片3cによつて錫製のチツプ
6が抱合せ圧着されている。 The fusible conductor 3 is made by connecting one end of the plate-shaped fusible conductor part 3a made of an alloy of brass and tin to the female terminal 4 by crimping or the like, as described above, and connecting the bent end to the other end. A tin chip 6 is crimped onto the piece 3b by a claw piece 3c.
この可溶導体3に溶断限界電流付近の電流が流
れ、その温度が400℃前後に達すると、抱合せ固
定されたチツプ6の錫が加熱され徐々に拡散しは
じめる。この際、可溶導体3自体が錫入り合金で
あるためチツプ6に対する親和性が強く、錫が拡
散し易くなる。次いで、温度が約470℃以上にな
ると、β相の結晶格子内の原子配置が整列から不
整列への相変化を起し、電気的抵抗が急激に増加
する。その結果、前記チツプ6の錫の拡散現象と
の相乗効果により、合金化が更に進行して融点が
下がり、温度上昇から溶断までの時間を著しく短
縮することができる。 A current near the fusing limit current flows through the fusible conductor 3, and when the temperature reaches around 400°C, the tin of the chip 6 that is bound and fixed is heated and gradually begins to diffuse. At this time, since the fusible conductor 3 itself is a tin-containing alloy, it has a strong affinity for the chips 6, making it easier for tin to diffuse. Next, when the temperature rises to about 470° C. or higher, the atomic arrangement within the crystal lattice of the β phase undergoes a phase change from aligned to misaligned, resulting in a rapid increase in electrical resistance. As a result, due to the synergistic effect with the diffusion phenomenon of tin in the chips 6, alloying further progresses and the melting point decreases, making it possible to significantly shorten the time from temperature rise to melting.
本発明は以上説明したように、四六黄銅に0.5
〜3.0%の錫を添加したものであるから、β黄銅
よりも加工性に優れて生産性が向上し、四六黄銅
よりもβ相を多く含んだ電流感度の優れた可溶導
体用合金を提供することができる。 As explained above, the present invention has 0.5 to 46 brass.
Since it contains up to 3.0% tin, it has better workability and productivity than β-brass, and it contains more β-phase than Shiroku brass, making it an alloy for fusible conductors with excellent current sensitivity. can be provided.
また、温度上昇から溶断までの時間が短いため
より安全なヒユージブルリンクが製作でき、これ
は第2図に示す如く錫チツプ等との組合せにより
更に促進される。 Furthermore, since the time from temperature rise to melting is short, a safer fusible link can be manufactured, and this is further promoted by the combination with tin chips, etc., as shown in FIG.
更に、錫の添加により亜鉛の量と共に強くなる
脱亜鉛現象や応力腐食割れを抑制し、寿命の長い
ヒユージブルリンクとすることができる。 Furthermore, the addition of tin suppresses the dezincing phenomenon and stress corrosion cracking, which become stronger as the amount of zinc increases, resulting in a fusible link with a long life.
第1図は本発明合金と従来品の溶断特性を示す
グラフ、第2図は本発明合金を使用したヒユージ
ブルリンクの実施態様を示す説明図である。
1……ハウジング、2……カバー、3……可溶
導体、4……雌端子、5……ヒユージブルリン
ク、6……錫製のチツプ。
FIG. 1 is a graph showing the fusing characteristics of the alloy of the present invention and a conventional product, and FIG. 2 is an explanatory diagram showing an embodiment of a fusible link using the alloy of the present invention. 1... Housing, 2... Cover, 3... Fusible conductor, 4... Female terminal, 5... Fusible link, 6... Tin chip.
Claims (1)
とを特徴とする可溶導体用合金。1. A fusible conductor alloy characterized by adding 0.5 to 3.0% of tin to 46 brass.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6593084A JPS60211027A (en) | 1984-04-04 | 1984-04-04 | Alloys for fusible conductors |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6593084A JPS60211027A (en) | 1984-04-04 | 1984-04-04 | Alloys for fusible conductors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60211027A JPS60211027A (en) | 1985-10-23 |
| JPH0350822B2 true JPH0350822B2 (en) | 1991-08-02 |
Family
ID=13301167
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6593084A Granted JPS60211027A (en) | 1984-04-04 | 1984-04-04 | Alloys for fusible conductors |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60211027A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6141737A (en) * | 1984-07-31 | 1986-02-28 | Tamagawa Kikai Kinzoku Kk | Cu alloy for electric fuse |
| JP2624593B2 (en) * | 1991-12-12 | 1997-06-25 | 矢崎総業株式会社 | fuse |
| JP2015159035A (en) * | 2014-02-24 | 2015-09-03 | 旭化成ケミカルズ株式会社 | fuse housing |
-
1984
- 1984-04-04 JP JP6593084A patent/JPS60211027A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60211027A (en) | 1985-10-23 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |