JPH0683930B2 - EDM liquid - Google Patents

EDM liquid

Info

Publication number
JPH0683930B2
JPH0683930B2 JP2379186A JP2379186A JPH0683930B2 JP H0683930 B2 JPH0683930 B2 JP H0683930B2 JP 2379186 A JP2379186 A JP 2379186A JP 2379186 A JP2379186 A JP 2379186A JP H0683930 B2 JPH0683930 B2 JP H0683930B2
Authority
JP
Japan
Prior art keywords
discharge machining
electric discharge
weight
machining fluid
wear rate
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 - Lifetime
Application number
JP2379186A
Other languages
Japanese (ja)
Other versions
JPS62181828A (en
Inventor
立 西山
雅一 岸
隆久 増沢
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Via Mechanics Ltd
Original Assignee
Hitachi Seiko Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Hitachi Seiko Ltd filed Critical Hitachi Seiko Ltd
Priority to JP2379186A priority Critical patent/JPH0683930B2/en
Publication of JPS62181828A publication Critical patent/JPS62181828A/en
Publication of JPH0683930B2 publication Critical patent/JPH0683930B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)

Description

【発明の詳細な説明】 〔発明の利用分野〕 本発明は不燃性放電加工液に係り、特に放電加工時に生
成する不燃性放電加工液の分解ガスにより、悪臭を発生
しない不燃性放電加工液に関する。
Description: FIELD OF THE INVENTION The present invention relates to a non-combustible electric discharge machining fluid, and more particularly to a non-combustible electric discharge machining fluid that does not generate a bad odor due to a decomposed gas of the non-combustible electric discharge machining fluid generated during electric discharge machining. .

〔発明の背景〕[Background of the Invention]

従来、可燃性の鉱油系放電加工液に代る不燃性放電加工
液としては、ポリエチレングリコール、多価アルコール
の水溶液が提案されている。しかし、これらの不燃性放
電加工液は、加工中に不燃性放電加工液から分解生成し
たガスによる悪臭が発生する。そこで、上記の不燃性放
電加工液を使用する場合は、従来の鉱油系放電加工液使
用の場合と異なり、局所排気装置を設置しないと加工が
できないという問題点がある。
Conventionally, an aqueous solution of polyethylene glycol or a polyhydric alcohol has been proposed as a non-flammable electric discharge machining fluid instead of a flammable mineral oil-based electric discharge machining fluid. However, these nonflammable electric discharge machining liquids produce a bad odor due to the gas decomposed and produced from the nonflammable electric discharge machining liquid during machining. Therefore, when the above-mentioned non-flammable electric discharge machining liquid is used, there is a problem that machining cannot be performed unless a local exhaust device is installed, unlike the case where a conventional mineral oil-based electric discharge machining liquid is used.

また、不燃性放電加工液で、放電加工時に生成する不燃
性放電加工液での分解ガスが悪臭を発生しないものは、
放電加工特性が悪く実用できない問題点がある。
In addition, non-combustible electrical discharge machining liquids that do not produce a foul odor when decomposed by the non-combustible electrical discharge machining liquid generated during electrical discharge machining
There is a problem that the electrical discharge machining characteristics are poor and it cannot be used in practice.

〔発明の効果〕〔The invention's effect〕

本発明の目的は上記した従来技術の問題点をなくし、放
電加工特性が良好であり、かつ放電加工中に悪臭を発生
しない不燃性放電加工液を提供することにある。
It is an object of the present invention to provide a non-flammable electric discharge machining liquid which eliminates the above-mentioned problems of the prior art, has good electric discharge machining characteristics, and does not generate a bad odor during electric discharge machining.

〔発明の概要〕[Outline of Invention]

上記目的を達成するため、発明者は不燃性放電加工液に
ついて種々検討した結果、ポリオキシアルキレンアルキ
ルエーテル溶液が良いことを見い出した。なお、ポリオ
キシアルキレンアルキルエーテルは、下記一般式(1)
で示されるものがよく RO(R′O)nOH ……(1) 但し、上記一般式(1)中RはC12H25−、C13H27−、C
14H29−、C15H31−であり、R′は−CH2CH2−、−CH2CH
2CH2−、−CH2CH2CH2CH2−であり、nは14〜18であ
る。) なかでもRがC12H25−、R′が−CH2CH2−、nが17のポ
リオキシエチレンラウリルエーテル(分子式C12H25O−
(CH2CH2O)17−OH)が好ましい。
In order to achieve the above-mentioned object, the inventor has conducted various studies on non-combustible electric discharge machining liquid, and found that a polyoxyalkylene alkyl ether solution is preferable. The polyoxyalkylene alkyl ether has the following general formula (1)
In those shown well RO (R'O) nOH ...... (1) where the above general formula (1), R is C 12 H 25 -, C 13 H 27 -, C
14 H 29 −, C 15 H 31 −, and R ′ is —CH 2 CH 2 —, —CH 2 CH.
2 CH 2 -, - CH 2 CH 2 CH 2 CH 2 - and it is, n represents an 14 to 18. ) Among these R is C 12 H 25 -, R 'is -CH 2 CH 2 -, polyoxyethylene lauryl ether n is 17 (molecular formula C 12 H 25 O-
(CH 2 CH 2 O) 17 -OH) are preferred.

そして、上記のポリオキシアルキレンアルキルエーテル
の水溶液は、ポリオキシアルキレンアルキルエーテルの
割合が10ないし30重量%溶液がよく、15ないし30重量%
溶液が、更に好ましく、20重量%溶液が最も好ましい。
The polyoxyalkylene alkyl ether aqueous solution is preferably a solution containing 10 to 30% by weight of polyoxyalkylene alkyl ether, and 15 to 30% by weight.
Solutions are more preferred, with 20% by weight solutions being most preferred.

また、上記のポリオキシアルキルエーテル水溶液に、シ
リコーン系消泡剤を配合してもよく、配合割合はポリオ
キシアルキレンアルキルエーテル水溶液99〜99.99重量
%に対して、シリコーン系消泡剤1〜0.01重量%であ
り、好ましくはポリオキシアルキレンアルキルエーテル
水溶液99.5〜99.95重量%、シリコーン系消泡剤0.5〜0.
05重量%である。
Further, the above polyoxyalkyl ether aqueous solution may be blended with a silicone antifoaming agent, and the blending ratio is 1 to 0.01 weight% of the silicone antifoaming agent with respect to 99 to 99.99% by weight of the polyoxyalkylene alkyl ether aqueous solution. %, Preferably 99.5 to 99.95% by weight of polyoxyalkylene alkyl ether aqueous solution, 0.5 to 0.
It is 05% by weight.

シリコーン系消泡剤としては、たとえばジメチルポリシ
ロキサン を用いる。この化学合物は、ポリオキシアルキレングリ
コール誘導体に添加して用いるのが好ましい。
Examples of the silicone-based defoaming agent include dimethyl polysiloxane To use. This chemical compound is preferably used by adding it to a polyoxyalkylene glycol derivative.

〔発明の実施例〕Example of Invention

以下、本発明を実施例によって詳細に説明する。 Hereinafter, the present invention will be described in detail with reference to examples.

実施例1 C12H25O−(CH2CH2O)17−OH5g、10g、15g、20g、30g、
35gと導電率10μS/cmの純水95g、90g、85g、80g、70g、
65gとを混合し、C12H25O−(CH2CH2O)17−OHの5重量
%、15重量%、20重量%、30重量%、35重量%溶液の不
燃性放電加工液を作成した。
Example 1 C 12 H 25 O- (CH 2 CH 2 O) 17 -OH5g, 10g, 15g, 20g, 30g,
35g and pure water 95g, 90g, 85g, 80g, 70g with conductivity of 10μS / cm,
65g is mixed with a non-combustible electric discharge machining solution of 5% by weight, 15% by weight, 20% by weight, 30% by weight and 35% by weight of C 12 H 25 O- (CH 2 CH 2 O) 17 -OH. Created.

そして、上記の6種類の放電加工液中で、電極にはグラ
ファイト電極(直径25mm)を用い、SKD1の放電加工を放
電ピーク電流52A、印加パルス巾1000μSにて行なっ
た。そして、加工速度、電極消耗率、加工面粗さを求め
ると共に、放電加工液分解ガスの臭気、不燃性か否かを
調べた。
Then, in the above 6 kinds of electric discharge machining liquids, graphite electrodes (diameter 25 mm) were used as electrodes, and electric discharge machining of SKD1 was performed with a discharge peak current of 52 A and an applied pulse width of 1000 μS. Then, the machining speed, the electrode wear rate, and the machined surface roughness were obtained, and it was examined whether or not the odor of the gas decomposed by the electric discharge machining was nonflammable.

測定結果は第1表に示すとうりであり、10ないし30重量
%の範囲で良好な特性を示すことがわかった。
The measurement results are as shown in Table 1, and it was found that good characteristics were exhibited in the range of 10 to 30% by weight.

実施例2 ポリオキシエチレンラウリルエーテルの20重量%水溶液
中で、グラファイト電極(直径25mm)を用いて放電ピー
ク電流52A、印加パルス巾30ないし1000μSにてSKD1の
放電加工実験を行なった。
Example 2 An electric discharge machining experiment of SKD1 was carried out in a 20% by weight aqueous solution of polyoxyethylene lauryl ether using a graphite electrode (diameter 25 mm) with a discharge peak current of 52 A and an applied pulse width of 30 to 1000 μS.

また、比較のため鉱油系放電加工油と、導電率10μS1cm
の純水80重量%を用いて、上記の同一条件で放電加工を
行なった。
Also, for comparison, mineral oil-based electric discharge machining oil and conductivity 10 μS 1 cm
The electric discharge machining was performed under the same conditions as above, using 80% by weight of pure water.

第1図に加工速度とパルス巾との関係を示す。純水の放
電加工速度3は鉱油系放電加工油の放電加工速度2の50
%以下であるのに対して、本発明の放電加工液の放電加
工速度1はパルス巾が100μS以上の領域で鉱油系放電
加工油の160ないし260%となる。第2図に電極消耗率
(体積消耗比)とパルス巾との関係を示す。純水の電極
消耗率6は消耗15%以下の加工は不可能であることを示
している。それに対して、本発明の放電加工液の電極消
耗率4はパルス巾100μS以上の領域で鉱油系放電加工
油の電極消耗率5に近い1%前後以下の加工を実現して
いる。
FIG. 1 shows the relationship between the processing speed and the pulse width. The electric discharge machining speed 3 of pure water is 50 which is the electric discharge machining speed 2 of mineral oil type electric discharge machining oil.
%, The electric discharge machining speed 1 of the electric discharge machining fluid of the present invention is 160 to 260% of that of the mineral oil type electric discharge machining oil in the region where the pulse width is 100 μS or more. FIG. 2 shows the relationship between the electrode wear rate (volume wear ratio) and the pulse width. The electrode wear rate 6 of pure water indicates that processing with a wear rate of 15% or less is impossible. On the other hand, the electrode wear rate 4 of the electric discharge machining fluid of the present invention realizes a machining of about 1% or less, which is close to the electrode wear rate 5 of the mineral oil type electric discharge machine oil in the region of the pulse width of 100 μS or more.

また、本発明の放電加工液を使用したときの工作物の加
工面粗さは放電加工油による面粗さと同等であった。
The surface roughness of the workpiece when the electric discharge machining fluid of the present invention was used was equivalent to the surface roughness due to the electric discharge machining oil.

第3図、第4図はポリオキシエチレンラウリルエーテル
の濃度と加工性能の関係である。ポリオキシエチレンラ
ウリルエーテル濃度は、0ないし30重量%とした。な
お、30重量%以上の濃度では、粘度が高くなり、加工は
不可能である。第3図はピーク電流52A、パルス巾1000
μSで加工したときの加工速度とポリオキシエチレンラ
ウリルエーテル水溶液濃度の関係である。濃度が10重量
%までは加工速度の増加が著しく、10重量%以上の濃度
で加工速度が飽和する。これに対して電極消耗率は、第
4図に示すように濃度10重量%以上で消耗率が5%以
下、濃度15重量%以上で消耗率1%以下の性能が得られ
る。
FIG. 3 and FIG. 4 show the relationship between the concentration of polyoxyethylene lauryl ether and the processing performance. The polyoxyethylene lauryl ether concentration was 0 to 30% by weight. At a concentration of 30% by weight or more, the viscosity becomes high and processing is impossible. Fig. 3 shows a peak current of 52A and a pulse width of 1000.
It is the relationship between the processing speed and the polyoxyethylene lauryl ether aqueous solution concentration when processing with μS. The processing speed increases remarkably up to a concentration of 10% by weight, and the processing speed is saturated at a concentration of 10% by weight or more. On the other hand, as for the electrode wear rate, as shown in FIG. 4, the performance is such that the wear rate is 5% or less when the concentration is 10 wt% or more, and the wear rate is 1% or less when the concentration is 15 wt% or more.

また、加工中、加工液面上に気泡が多量に発生したが、
ジメチルポリシロキサンを消泡剤として0.01ないし1重
量%添加して、加工特性を変えずに発泡を抑えることが
できた。
Also, during processing, a large amount of bubbles were generated on the surface of the processing liquid,
By adding 0.01 to 1% by weight of dimethylpolysiloxane as an antifoaming agent, foaming could be suppressed without changing the processing characteristics.

比較例 従来提案されている水溶液である、エチレングリコール
水溶液の30重量%のものを使って、上記の加工条件と同
じ、ピーク電流52A、パルス巾1000μSで加工を行っ
た。その結果、加工速度は120mm3/min電極消耗率は7.7
%、加工面粗さは75μmRmaxであった。
Comparative Example Using a conventionally proposed aqueous solution of 30% by weight of an ethylene glycol aqueous solution, processing was carried out under the same processing conditions as above with a peak current of 52 A and a pulse width of 1000 μS. As a result, the processing speed was 120 mm 3 / min and the electrode wear rate was 7.7.
%, The processed surface roughness was 75 μm Rmax.

ポリオキシエチレンラウリルエーテル水溶液の加工特性
と比較すると加工面粗さは優れているものの、加工速
度、電極消耗率はかなり劣っており、総合的に見てポリ
オキシエチレンラウリルエーテル水溶液が優れている。
またエチレングリコール水溶液での加工では、強いアル
デヒド臭が感じられ、著しく作業環境を悪くする。
Compared with the processing characteristics of the polyoxyethylene lauryl ether aqueous solution, the processed surface roughness is excellent, but the processing speed and electrode wear rate are considerably inferior, and the polyoxyethylene lauryl ether aqueous solution is excellent overall.
In addition, processing with an ethylene glycol aqueous solution gives a strong aldehyde odor, which significantly deteriorates the working environment.

〔発明の効果〕〔The invention's effect〕

以上述べたように、本発明の不燃性放電加工液によれ
ば、不快な臭気を発生させずに、電極消耗率の低い放電
加工ができる。
As described above, according to the nonflammable electric discharge machining liquid of the present invention, it is possible to perform electric discharge machining with a low electrode consumption rate without generating an unpleasant odor.

【図面の簡単な説明】[Brief description of drawings]

第1図は各種放電加工液の加工速度とパルス巾の関係
図、第2図は各種放電加工液の電極消耗率とパルス巾の
関係図、第3図は放電加工液濃度と加工速度の関係図、
第4図は放電加工液濃度と電極消耗率の関係図である。 1……本発明の放電加工液の放電加工速度 2……鉱油系放電加工油の放電加工速度 3……純水の放電加工速度 4……本発明の放電加工液の電極消耗率 5……鉱油系放電加工油の電極消耗率 6……純水の電極消耗率
Fig. 1 shows the relationship between the machining speed and pulse width of various EDMs, Fig. 2 shows the relationship between the electrode wear rate and pulse width of various EDMs, and Fig. 3 shows the relationship between the EDM concentration and machining speed. Figure,
FIG. 4 is a diagram showing the relationship between the electric discharge machining liquid concentration and the electrode wear rate. 1 ... EDM speed of EDM of the present invention 2 ... EDM speed of mineral oil-based EDM oil 3 ... EDM speed of pure water 4 ... Electrode wear rate of EDM of the present invention 5 ... Electrode wear rate of mineral oil-based electric discharge machining oil 6 ... Electrode wear rate of pure water

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】一般式がRO(R′O)nOH(但しRはアル
キル基、R′はアルキレン基)で表わされるポリオキシ
アルキレンアルキルエーテルと、水よりなることを特徴
とする放電加工液。
1. An electric discharge machining fluid comprising a polyoxyalkylene alkyl ether represented by the general formula RO (R'O) nOH (where R is an alkyl group and R'is an alkylene group) and water.
【請求項2】前記Rがラウリル基(C12H25−)であり、
前記R′が−CH2CH2−であり、nが17のポリオキシエチ
レンラウリルエーテルであることを特徴とする請求範囲
第1項記載の放電加工液。
2. R is a lauryl group (C 12 H 25 —),
2. The electric discharge machining fluid according to claim 1, wherein R ′ is —CH 2 CH 2 — and n is polyoxyethylene lauryl ether.
【請求項3】前記ポリオキシアルキレンアルキルエーテ
ルの濃度が10ないし30重量%であることを特徴とする請
求範囲第2項記載の放電加工液。
3. The electric discharge machining fluid according to claim 2, wherein the concentration of the polyoxyalkylene alkyl ether is 10 to 30% by weight.
【請求項4】一般式がRO(R′O)nOH(但しRはアル
キル基、R′はアルキレン基)で表わされるポリオキシ
アルキレンアルキルエーテルと、水と、シリコーン系消
泡剤よりなることを特徴とする放電加工液。
4. A polyoxyalkylene alkyl ether represented by the general formula RO (R′O) nOH (where R is an alkyl group and R ′ is an alkylene group), water, and a silicone antifoaming agent. A characteristic EDM fluid.
【請求項5】前記シリコーン系消泡剤が0.01ないし1重
量%であることを特徴とする特許請求の範囲第4項記載
の放電加工液。
5. The electric discharge machining fluid according to claim 4, wherein the silicone antifoaming agent is 0.01 to 1% by weight.
【請求項6】前記シリコーン系消泡剤がジメチルポリシ
ロキサンであることを特徴とする特許請求の範囲第4項
記載の放電加工液。
6. The electric discharge machining fluid according to claim 4, wherein the silicone antifoaming agent is dimethylpolysiloxane.
JP2379186A 1986-02-07 1986-02-07 EDM liquid Expired - Lifetime JPH0683930B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2379186A JPH0683930B2 (en) 1986-02-07 1986-02-07 EDM liquid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2379186A JPH0683930B2 (en) 1986-02-07 1986-02-07 EDM liquid

Publications (2)

Publication Number Publication Date
JPS62181828A JPS62181828A (en) 1987-08-10
JPH0683930B2 true JPH0683930B2 (en) 1994-10-26

Family

ID=12120148

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2379186A Expired - Lifetime JPH0683930B2 (en) 1986-02-07 1986-02-07 EDM liquid

Country Status (1)

Country Link
JP (1) JPH0683930B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5081333A (en) * 1989-03-17 1992-01-14 Mitsubishi Denki Kabushiki Kaisha Electric discharge machining fluid with a fatty acid amide additive for rust inhibition

Also Published As

Publication number Publication date
JPS62181828A (en) 1987-08-10

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