JP2582357B2 - Electric machining method - Google Patents

Electric machining method

Info

Publication number
JP2582357B2
JP2582357B2 JP61235388A JP23538886A JP2582357B2 JP 2582357 B2 JP2582357 B2 JP 2582357B2 JP 61235388 A JP61235388 A JP 61235388A JP 23538886 A JP23538886 A JP 23538886A JP 2582357 B2 JP2582357 B2 JP 2582357B2
Authority
JP
Japan
Prior art keywords
working fluid
compound
processing
machining method
electrode
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 - Fee Related
Application number
JP61235388A
Other languages
Japanese (ja)
Other versions
JPS6389222A (en
Inventor
信之 高橋
茂男 森
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.)
DAIICHI KOGYO SEIYAKU KK
SODEITSUKU KK
Original Assignee
DAIICHI KOGYO SEIYAKU KK
SODEITSUKU KK
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 DAIICHI KOGYO SEIYAKU KK, SODEITSUKU KK filed Critical DAIICHI KOGYO SEIYAKU KK
Priority to JP61235388A priority Critical patent/JP2582357B2/en
Publication of JPS6389222A publication Critical patent/JPS6389222A/en
Application granted granted Critical
Publication of JP2582357B2 publication Critical patent/JP2582357B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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、電極と被工作物との間に断続的な放電を行
なわせて放電加工を行なう際、電極と被加工物との間に
介在させるための電気加工法に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Application of the Invention) The present invention relates to an electric discharge machining method in which an intermittent electric discharge is performed between an electrode and a work to be interposed between the electrode and the work. The present invention relates to an electric machining method for causing the electric machining.

(従来の技術) 放電加工法は、作業用電極と導電性被工作物との間の
絶縁性媒体内で断続的に火花放電させることにより、対
象物に形彫りを施したり、孔を穿ったり、又は対象物を
切断したりする技術である。この技術は、対象物の硬度
に影響されないこと、及び表面粗さ±0.2μm又はそれ
以下の鏡面仕上に近い加工精度を期待できること等の特
徴を買われて、今日各種の金属加工に広く利用されてい
る。
(Prior art) The electric discharge machining method performs engraving or drilling on an object by intermittently sparking in an insulating medium between a working electrode and a conductive workpiece. Or a technique for cutting an object. This technology is widely used in various metal processing today because of its features that it is not affected by the hardness of the object and that it can be expected to have a processing accuracy close to a mirror finish with a surface roughness of ± 0.2 μm or less. ing.

ところで、この放電加工法では、従来より上の絶縁性
媒体として、主として鉱油(ケロシン)が使用されてい
る。しかし、鉱油には引火性があるため、無人的に連続
加工を行なう場合には火災発生の危険がある。そこで近
来に至り純水の使用が試みられるようになって来た。な
お、本加工法では、加工効率を向上させるため絶縁性媒
体に添加剤を加えるのが有効であって、このための添加
剤に関しては従来から多くの提案があり、例えばエチレ
ングリコール、プロピレングリコールなどの極性溶媒類
や、ポリアクリル酸、ポリアクリルアミドなどの極性ポ
リマー、あるいはポリエチレングリコールのような非イ
オン性化合物などがそれである(例えば、特公昭59−4,
253号、特開昭60−71,120号又は特開昭61−4,623号など
の各公報参照)。
By the way, in this electric discharge machining method, a mineral oil (kerosene) is mainly used as an insulating medium higher than before. However, since mineral oil is flammable, there is a danger of a fire occurring if continuous processing is performed unattended. Therefore, the use of pure water has recently been attempted. In the present processing method, it is effective to add an additive to the insulating medium in order to improve the processing efficiency, and there have been many proposals for additives for this purpose, such as ethylene glycol and propylene glycol. And polar polymers such as polyacrylic acid and polyacrylamide, and nonionic compounds such as polyethylene glycol (for example, Japanese Patent Publication No. 59-4,
253, JP-A-60-71,120 or JP-A-61-4,623).

しかしながら、これらの添加剤は、加工速度を著しく
向上させるにも拘らず、現在に至るも殆ど実用化の見通
しが立っていない。この理由の主なものは、水性加工液
では鉱油系加工液の場合と異なり、電極の消耗率を実用
レベルである1%以下に低下させるのが困難なことであ
る(鉱油系加工液では、加工速度の増加に半比例して電
極消耗率が低下する)。
However, despite the fact that these additives significantly increase the processing speed, there is almost no prospect of practical use up to the present. The main reason for this is that it is difficult to reduce the consumption rate of the electrode to 1% or less, which is a practical level, in the case of the aqueous working fluid, unlike the case of the mineral oil-based working fluid. The electrode consumption rate is reduced in proportion to the increase in the processing speed).

以上に加えて、過去の有力に見える提案が、いづれも
実用段階に至らないなお主要な原因は、電極の異常消耗
である。即ち、ケロシンあるいは水に極性の有機化合物
を添加した加工液は、見かけの電極消耗(重量測定によ
る)とは別に、電極の部分的消耗や加工鉄粉の再付着に
よる形状変化などの異状が発生するため、結果として電
流量を下げざるを得ず、ひいては低能率の加工を余儀な
くされているのが現状である。
In addition to the above, one of the main causes that none of the past promising proposals have reached the practical stage is abnormal wear of the electrodes. That is, the working fluid in which a polar organic compound is added to kerosene or water causes abnormalities such as partial wear of the electrodes and a change in shape due to reattachment of the working iron powder, apart from apparent electrode consumption (by weight measurement). As a result, the current amount has to be reduced as a result, and as a result, low-efficiency machining is inevitable.

(発明の目的) 本発明は、電極消耗率が画期的に近く、長時間に亘り
連続使用しても、該率を精々1%又はそれ未満に保つこ
とができ、しかも異常消耗もなく、かつ、加工不良も生
じない実用的な電気加工法を提供するのを目的とする。
(Object of the Invention) The present invention has an electrode wear rate that is close to an epoch-making, and even when used continuously for a long time, can keep the rate at most 1% or less, and furthermore, there is no abnormal wear. It is another object of the present invention to provide a practical electric machining method that does not cause machining defects.

(目的達成のための手段) 本発明者は、多数の新規及び公知の有機物質について
精力的な研究を行なった結果、加工液中に浸漬されてい
る被加工材にパルス電流を放電して加工するにあたり、
該加工液に、別工程により予め、その水溶液の抵抗値が
2万Ωcm以上となるようイオン性物質の少なくとも大部
分が除去されている、該加工液と相溶性のポリオキシア
ルキレン鎖を含有する非イオン性化合物を添加すること
により、比抵抗値の安定した加工液による良好な加工が
なされ、電極消耗率が画期的に低く、長時間に亘り連続
使用しても、該率を精々1%又はそれ未満に保つことが
でき、しかも電極の異常消耗も起こらない実用的な電気
加工法を提供できることを見出した。
(Means for Achieving the Object) As a result of intense research on a number of new and known organic substances, the present inventor has performed processing by discharging a pulse current to a work material immersed in a working fluid. In doing so
The working fluid contains a polyoxyalkylene chain compatible with the working fluid in which at least most of the ionic substance has been removed in advance by another process so that the resistance value of the aqueous solution is 20,000 Ωcm or more. By adding a nonionic compound, good working with a working fluid having a stable specific resistance value is performed, the electrode wear rate is remarkably low, and even if the electrode is used continuously for a long time, the rate can be reduced to 1 at most. % Or less, and it has been found that a practical electric machining method can be provided that does not cause abnormal consumption of the electrode.

本発明の実施に有用な、加工液と相溶性を有するポリ
オキシレン鎖を有する非イオン性化合物の例としては、
ポリエチレングリコール、非イオン界面活性剤又は炭素
数3以上のオキシアルキレン基を含有する下記化合物な
どがあるが、これ以外の残基として、RO(式中
Rは炭素数3〜8のアルキル基、aは3〜6の整数)、
−φ−O−、−C≡C−、CH2=CH−CH2−又は−S−な
どの基を含有しても差支えない。但し、該非イオン性化
合物は、予め別工程により、その水溶液の抵抗値が2万
Ωcm以上となるよう夾雑イオン性物質を除されている必
要がある。
Examples of nonionic compounds having a polyoxylene chain that is compatible with the working fluid, useful in the practice of the present invention, include:
Polyethylene glycol, nonionic surfactant or there are such following compounds containing 3 or more oxyalkylene group having a carbon as a residue other than this, RO a (wherein R is an alkyl group having 3 to 8 carbon atoms, a is an integer of 3 to 6),
-Φ-O -, - C≡C-, CH 2 = CH-CH 2 - or -S- no problem also contain groups such as. However, it is necessary that the non-ionic compound be previously removed from contaminating ionic substances by a separate process so that the aqueous solution has a resistance value of 20,000 Ωcm or more.

即ち、一般のポリオキシアルキレン化合物は、その製
造時に触媒として塩基性又は酸性触媒を用いて製造され
るから、特別な場合を除いて触媒の中和塩を含んでいる
のが常識である。これら触媒の中和塩は、通常200P.P.m
乃至500P.P.mにも達し、これらの中和塩が結果として加
工液中に混入した場合、加工液の比抵抗値を著しく低下
せしめるため、良好な加工が不可能となる。このため、
加工液に添加される加工促進剤は、イオン性物質が少な
い程好ましく、具体的には、その水溶液抵抗値として通
常2万Ωcm以上必要である。
That is, since a general polyoxyalkylene compound is produced using a basic or acidic catalyst as a catalyst at the time of its production, it is common knowledge that it contains a neutralized salt of the catalyst except in special cases. The neutralized salt of these catalysts is usually 200 PPm
To reach to 500 PPm, if these neutralized salt is mixed into the working fluid as a result, the allowed to decrease significantly the resistivity value of the machining fluid, it becomes impossible good processability. For this reason,
The processing accelerator added to the processing liquid is preferably as small as possible in the amount of ionic substance. Specifically, the aqueous solution usually needs to have an aqueous solution resistance of 20,000 Ωcm or more.

因に、本発明に於ける非イオン性化合物から夾雑物す
るイオン性物質を除去する方法としては、一般的には既
にいくつかの提案があり、例えば、特公昭37−5,597
号、同昭41−21,237号、同昭45−33,194号、同昭52−1
0,018号、米国特許第4,316,948号などがある。本発明で
は、これらどの方法を採用してもよいが、これらイオン
性物質は、少なくとも加工液に配合される以前に、別工
程で非イオン性化合物の水溶液の抵抗値が2万Ωcm以上
となるよう除去されていなければならない。その理由
は、加工機に付属する小型の脱イオン装置には、加工液
自体の比抵抗値を一定に維持するのに必要にして充分な
程度の能力しかないため、加工液に添加される薬剤から
の大量の混入イオンの排除が非常に困難であり、そして
万一イオン性物質が加工液中に大量に混入すると、脱イ
オン装置に過負荷がかかるのみでなく、脱イオン機能が
急速に低下するため加工液の比抵抗値が不安定になって
良好な加工が不能となるからである。
Incidentally, as a method for removing contaminating ionic substances from a nonionic compound in the present invention, generally, there have already been some proposals, for example, Japanese Patent Publication No. 37-5597.
No. 41-21,237, No. 45-33,194, No. 52-1
No. 0,018 and U.S. Pat. No. 4,316,948. In the present invention, any of these methods may be employed, however, these ionic substances have a resistance value of an aqueous solution of a non-ionic compound of at least 20,000 Ωcm in a separate step, at least before being blended into the working fluid. Must be removed. The reason is that the small deionizer attached to the processing machine has only the necessary and sufficient capacity to keep the specific resistance value of the processing fluid itself constant, It is very difficult to remove large amounts of contaminating ions from the wastewater, and if a large amount of ionic substances is mixed into the working fluid, not only will the deionizer be overloaded, but also the deionization function will decrease rapidly. This is because the specific resistance of the working fluid becomes unstable and good working becomes impossible.

(実施例) 以下、実施例により発明実施の態様を説明するが、例
示が、直接発明思想の内包・外延を限るものではないこ
とは当然である。
(Examples) Hereinafter, embodiments of the invention will be described with reference to examples. However, it is needless to say that exemplification does not directly limit inclusion and extension of the invention idea.

参考例1 表−1に示すポリオキシアルキレン化合物を公知の方
法で重合させた。
Reference Example 1 The polyoxyalkylene compounds shown in Table 1 were polymerized by a known method.

実施例2 実施例1の化合物に2%量の合成硅酸アルミニウムを
添加し、オートクレーブ中、120℃で6時間撹拌したの
ち、固形分を濾過して表−2の精製物を得た。
Example 2 A 2% amount of synthetic aluminum silicate was added to the compound of Example 1, and the mixture was stirred in an autoclave at 120 ° C for 6 hours, and the solid content was filtered to obtain a purified product shown in Table-2.

実施例−3 表−1の化合物A−1及び表−2の化合物B−1をイ
オン交換純水中に溶解させたのち、比抵抗値を測定した
ところ第1図の通りであった。但し、図中−○−で示さ
れる曲線は化合物B−1の、−●−で示される曲線は化
合物A−1のデータを夫々示す。
Example-3 After dissolving the compound A-1 in Table 1 and the compound B-1 in Table 2 in ion-exchanged pure water, the specific resistance was measured, and the result was as shown in FIG. However, in the figure, the curve indicated by -O- indicates the data of the compound B-1, and the curve indicated by-●-indicates the data of the compound A-1.

実施例−4 実施例−3のA−1及びB−1の化合物を用いて表−
3の条件で加工実験を行った。
Example-4 Table using the compounds of A-1 and B-1 of Example-3
A processing experiment was performed under the conditions of No. 3.

結果を第2図及び第3図に示す。 The results are shown in FIGS. 2 and 3.

曲線−○−で示される化合物B−1を使用した場合は
添加剤の濃度を50%まで高めても異常放電が起こらず、
加工速度を向上させることができたが、−×−で示され
る対照化合物A−1を用いた場合は、2%程度の低濃度
でも異常放電を起こし、加工が不能となった。
When the compound B-1 represented by the curve-○-was used, no abnormal discharge occurred even when the concentration of the additive was increased to 50%.
Although the processing speed could be improved, when the control compound A-1 represented by -x- was used, abnormal discharge occurred even at a low concentration of about 2%, and the processing became impossible.

(効果) 以上説明したとおり、本発明は、別工程により予め、
その水溶液の抵抗値が2万Ωcm以上となるようイオン性
物質の少なくとも大部分が除去されている非イオン性化
合物を加工液に添加して加工するため、加工液の比抵抗
値が安定し良好な加工がなされ、かつ、電極消耗率が画
期的に低く長時間に亘り連続運転しても、該率を精々1
%又はそれ未満に保つことができ、しかも異常消耗もな
い実用的な電気加工法を提供できるという結果を通じて
精密工作技術の発展に寄与しうる。
(Effects) As described above, the present invention provides
A non-ionic compound from which at least most of the ionic substance has been removed is added to the working fluid so that the resistance value of the aqueous solution is 20,000 Ωcm or more, and the working fluid is processed. Processing is performed, and the electrode wear rate is remarkably low.
% Or less, and can contribute to the development of precision machining technology through the result that a practical electric machining method without abnormal wear can be provided.

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

第1図は、被検化合物の純水中における濃度と比抵抗値
との関係を示すグラフ、第2図は、被検化合物の濃度と
加工速度との関係を示すグラフ、第3図は、被検化合物
の濃度と電極消耗率との関係を示すグラフである(符号
の説明は図中に併記)。
FIG. 1 is a graph showing the relationship between the concentration of the test compound in pure water and the specific resistance value, FIG. 2 is a graph showing the relationship between the concentration of the test compound and the processing speed, and FIG. 4 is a graph showing the relationship between the concentration of a test compound and the electrode consumption rate (the description of the symbols is also shown in the figure).

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】加工液中に浸漬されている被加工材にパル
ス電流を放電して加工するにあたり、該加工液に、別工
程により予め、その水溶液の抵抗値が2万Ωcm以上とな
るようイオン性物質の少なくとも大部分が除去されてい
る、該加工液と相溶性のポリオキシアルキレン鎖を含有
する非イオン性化合物を添加することを特徴とする電気
加工法。
When a pulse current is discharged to a workpiece immersed in a working fluid and the working fluid is processed, the working fluid is preliminarily subjected to another process so that the aqueous solution has a resistance value of 20,000 Ωcm or more. An electric processing method comprising adding a nonionic compound containing a polyoxyalkylene chain compatible with the working fluid, from which at least most of the ionic substance has been removed.
JP61235388A 1986-10-01 1986-10-01 Electric machining method Expired - Fee Related JP2582357B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61235388A JP2582357B2 (en) 1986-10-01 1986-10-01 Electric machining method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61235388A JP2582357B2 (en) 1986-10-01 1986-10-01 Electric machining method

Publications (2)

Publication Number Publication Date
JPS6389222A JPS6389222A (en) 1988-04-20
JP2582357B2 true JP2582357B2 (en) 1997-02-19

Family

ID=16985341

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61235388A Expired - Fee Related JP2582357B2 (en) 1986-10-01 1986-10-01 Electric machining method

Country Status (1)

Country Link
JP (1) JP2582357B2 (en)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5882629A (en) * 1981-11-10 1983-05-18 Mitsubishi Electric Corp Electric discharge machining device
JPS597529A (en) * 1982-07-02 1984-01-14 Mitsubishi Electric Corp Electrical discharge machining liquid
CH655031A5 (en) * 1983-07-29 1986-03-27 Charmilles Sa Ateliers MACHINING FLUID FOR ELECTRO-EROSIVE DISCHARGE MACHINING MACHINES.

Also Published As

Publication number Publication date
JPS6389222A (en) 1988-04-20

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