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JPH0224869B2 - - Google Patents
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JPH0224869B2 - - Google Patents

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Publication number
JPH0224869B2
JPH0224869B2 JP57114273A JP11427382A JPH0224869B2 JP H0224869 B2 JPH0224869 B2 JP H0224869B2 JP 57114273 A JP57114273 A JP 57114273A JP 11427382 A JP11427382 A JP 11427382A JP H0224869 B2 JPH0224869 B2 JP H0224869B2
Authority
JP
Japan
Prior art keywords
water
varnish
dispersed
dispersed varnish
liquid
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
JP57114273A
Other languages
Japanese (ja)
Other versions
JPS594664A (en
Inventor
Aiichiro Hashizume
Wataru Mifuji
Yukio Yamamoto
Hideki Chidai
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.)
Mitsubishi Electric Corp
Original Assignee
Mitsubishi Electric Corp
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 Mitsubishi Electric Corp filed Critical Mitsubishi Electric Corp
Priority to JP11427382A priority Critical patent/JPS594664A/en
Publication of JPS594664A publication Critical patent/JPS594664A/en
Publication of JPH0224869B2 publication Critical patent/JPH0224869B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は水に分散されたマイカ粉と水分散型ワ
ニスからなる電着塗料の製造法に関する。さらに
詳しくは、電気泳動法により電気導体上に電着絶
縁層を形成するのに用いられる無機絶縁材料であ
るマイカ粉と有機絶縁材料である水分散型ワニス
と水とからなる電着塗料を製造するに際し、それ
らを調合するまえに、あらかじめ水分散型ワニス
に限外過または逆浸透処理を行ない、絶縁用マ
イカのバインダーとして好適な水分散型ワニスの
液比抵抗の調整と水分散型ワニス中の雑イオンを
除去せしめることを特徴とする電着塗料の製造法
に関する。 マイカ粉を単独で用いて電気導体上に電着させ
る方法では、形成される電着絶縁層の強度が充分
でなく、電気導体を電着塗料から取り出す際に電
着絶縁層を形成しているマイカが流れ落ちる欠点
があつた。このため水分散型ワニスをマイカ粉の
バインダーとして用いることにより電気絶縁層の
機械的強度および電気的特性を向上させた電着塗
料およびその製造法が知られている(特開昭51−
89178号公報、特開昭51−114602号公報、参照)。 このマイカ粉と水分散型ワニスからなる電着塗
料を用いて製造した電着絶縁層の機械的強度およ
び電気的特性を支配する要因は、主として電着絶
縁層のマイカ含有率、マイカ粉の大きさおよび電
気絶縁層の含水率であり、いずれも電着塗料の調
製段階で制御しうる。 しかしながら、マイカ粉と水分散型ワニスを共
電着させるばあい、一般に水分散型ワニスの表面
電荷密度の方がマイカ粉のそれより大きく、した
がつて電位は水分散型ワニスの方がはるかに大き
いこと、またマイカ粉の重量が大きすぎることな
どにより、電気泳動速度が極端に異なり、その結
果電着槽内の電着塗料と電着絶縁層の組成が大き
く食違つてくるという現象が生ずる。 本発明者らはこの欠点を解決する方法として、
マイカ粉と水分散型ワニスの電気泳動速度が同じ
であれば電着槽内の電着塗料の組成と電気絶縁層
の組成が一定になることから、マイカ粉を水に分
散させたマイカ粉分散液と水分散型ワニスの液比
抵抗を同程度にして電気泳動速度を同等にする方
法を種々試みた。 その1例として、透析チユーブあるいは電気透
析法により水分散型ワニスの液比抵抗を調整する
方法を用いるときは、水分散型ワニス中の雑イオ
ンが除去できるため、雑イオン中の負のイオンが
水を随伴して正電極すなわち電気導体へと泳動す
ることがなくなり、その結果電気絶縁層の含水率
が低下し、マイカ粉が電気導体表面に密にしかも
平行に配列して電気絶縁層の機械的強度を向上せ
しめうることが判明した。 しかしながら、透析チユーブ法あるいは電気透
析法では水分散型ワニスの液比抵抗の調整および
雑イオン除去に長時間かかり、透析チユーブを用
いたばあいにはいわゆるバツチ方式となり多量の
水分散型ワニスを処理するためには多くの人手を
要すること、また透析チユーブ自身の強度の面か
ら連続使用が困難であるという欠点があつた。 本発明者らは多量の水分散型ワニスの液比抵抗
の調整および雑イオンの除去を短時間でかつ連続
的に行なうことができる方法として、限外過あ
るいは逆浸透法による方法を見出した。 すなわち本発明は、マイカ粉と水分散型ワニス
を水に分散するまえに、マイカ粉と水分散型ワニ
スの電気泳動速度を同等にするため、水分散型ワ
ニスの液比抵抗の調整および雑イオンの除去を限
外過または逆浸透処理で行なうことを特徴とす
る電着塗料の製造法に関する。 本発明における限外過あるいは逆浸透処理に
用いる透過膜は公知のものでよい。また水分散型
ワニスの濃度は5〜30重量%が適当であり、液比
抵抗は1000〜5000Ωcmが適当である。 つぎに図面に基づき本発明の方法を説明する。
第1図は本発明に用いる水分散型ワニスの液比抵
抗の調整および雑イオン除去のための処理装置の
概略図である。1は水分散型ワニスを入れる原液
タンク、2は水分散型ワニス、3は水分散型ワニ
ス用の配管、4aは水分散型ワニスを流すための
ポンプ、4bは再生透過液をタンク1に戻すため
のポンプ、5aは透過膜に流入する水分散型ワニ
スの流量および圧力を調整する弁、5bは透過膜
から流出する水分散型ワニスの流量および圧力を
調整する弁、6aは透過膜入口の圧力計、6bは
透過膜出口の圧力計、7は透過膜、8は透過水再
生のためのイオン交換樹脂、9は透過液の流れ、
10は再生透過液を入れるタンク、11は再生透
過液である。 この処理装置のタンク1に水分散型ワニスとイ
オン交換水を入れ、イオン交換水で希釈された水
分散型ワニスはポンプ4aにより透過膜7に送ら
れ、透過膜7により濃縮液と透過液に分離され
る。濃縮された水分散型ワニスはタンク1に戻さ
れ、一方透過液はイオン交換樹脂8で再生されて
タンク10に入る。タンク10の再生透過水11
はポンプ4bでタンク1に戻される。これを数回
繰り返すことで水分散型ワニスの液比抵抗の調整
と雑イオンの除去を行なうことができる。 つぎに本発明に用いる水分散型ワニスは、たと
えばエピコート1001(シエル化学社製のエポキシ
樹脂)100部、テトラヒドロ無水フタル酸25部お
よびエチレングリコール6部から酸価30〜60の酸
付加エポキシ樹脂を調製し、この樹脂をアンモニ
アを含む温水中に分散させたのちチツ素ガスを吹
き込むことによりえられる。 つぎに実施例および比較例をあげて本発明の方
法を説明する。なお、以下の実施例および比較例
では、PH7.0、不揮発分8.0%、液比抵抗250Ωcmの
ものを用いた。 実施例 1 水分散型ワニス30と5MΩcm以上のイオン交
換水30をタンク1に入れ、約12/分の流速で
透過膜を通過させ、濃縮液はタンク1に戻し、約
2/10分の割合で透過される透過液を1時間ご
とに約10の割合でタンク1に戻すことを約6回
繰り返したのち、透過液をタンク1に戻すことを
停止し、余分なイオン交換水を透過させて、9時
間後にPH7.0、不揮発分7.90%、液比抵抗2000Ωcm
の水分散型ワニスをえた。 この水分散型ワニスの固形分20部に対し、イオ
ン交換水でよく水洗いした35メツシユパスのマイ
カ粉を80部混合し、イオン交換水を加えてよく撹
拌し、均一に分散した不揮発分15%の電着塗料を
調製した。 この電着塗料中にあらかじめ形成した亀甲形の
コイルを浸漬し、極間距離50cmで対向電極との間
に直流電圧100Vを20秒間印加して、コイル上に
電着絶縁層を形成した。形成された絶縁層の膜層
および組成を調べた結果を第1表に示す。 実施例 2 実施例1で調製した水分散型ワニスの固形分30
部およびマイカ粉70部を用いたほかは実施例1と
同様の方法によりコイルに絶縁層を形成した。え
られた絶縁層の膜厚および組成を第1表に示す。 実施例 3 実施例1で調製した水分散型ワニスの固形分10
部およびマイカ粉90部を用いたほかは実施例1と
同様の方法により絶縁層を形成した。えられた絶
縁層の膜厚および組成を第1表に示す。 比較例 1 PH7.0、不揮発分8.0%、液比抵抗250Ωcmの前記
水分散型ワニス30を数個の透析チユーブ
(VISKINGチユーブ:白井松器械製)に入れ、
5MΩcm以上のイオン交換水を30入れた3つの
容器に透析チユーブに入れた水分散型ワニスを10
ずつ浸漬し、96時間後にPH6.8、不揮発分7.5
%、液比抵抗2000Ωcmの水分散型ワニスをえた。 この水分散型ワニスの固形分20部に対し、イオ
ン交換水でよく水洗いした35メツシユパスのマイ
カ粉80部を混合したのち、実施例1と同様な方法
でコイルに絶縁層を形成した。えられた絶縁層の
膜厚および組成を第1表に示す。 比較例 2 比較例1で調製した水分散型ワニスの固形分10
に対し、イオン交換水でよく水洗いした35メツシ
ユパスのマイカ粉90部を混合したのち、実施例1
と同様な方法でコイルに絶縁層を形成した。えら
れた絶縁層の膜厚および組成を第1表に示す。 【表】
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing an electrodeposition paint comprising mica powder dispersed in water and a water-dispersible varnish. More specifically, we manufacture electrodeposition paints made of mica powder, an inorganic insulating material used to form an electrodeposited insulating layer on electrical conductors by electrophoresis, water-dispersible varnish, an organic insulating material, and water. Before mixing them, the water-dispersed varnish is subjected to ultrafiltration or reverse osmosis treatment to adjust the liquid specific resistance of the water-dispersed varnish, which is suitable as a binder for insulating mica. The present invention relates to a method for producing an electrodeposition paint, which is characterized by removing miscellaneous ions. In the method of electrodepositing mica powder alone onto an electrical conductor, the strength of the electrodeposited insulating layer formed is not sufficient, and when the electrical conductor is removed from the electrodeposition paint, the electrodeposited insulating layer is formed. There was a defect that the mica ran down. For this reason, an electrodeposition paint and its manufacturing method are known in which the mechanical strength and electrical properties of an electrically insulating layer are improved by using a water-dispersed varnish as a binder for mica powder (Japanese Patent Application Laid-Open No. 51-197-1).
89178, JP-A-51-114602, see). The factors governing the mechanical strength and electrical properties of an electrodeposited insulating layer manufactured using an electrodeposition paint consisting of mica powder and water-dispersed varnish are mainly the mica content of the electrodeposited insulating layer and the size of the mica powder. and the water content of the electrically insulating layer, both of which can be controlled at the stage of preparing the electrodeposition paint. However, when co-electrodepositing mica powder and water-dispersed varnish, the surface charge density of the water-dispersed varnish is generally larger than that of the mica powder, so the potential is much higher for the water-dispersed varnish. Due to the large size of the mica powder and the excessive weight of the mica powder, the electrophoresis speed is extremely different, resulting in a phenomenon in which the compositions of the electrodeposited paint and the electrodeposited insulating layer in the electrodeposition tank differ greatly. . As a method to solve this drawback, the present inventors
If the electrophoresis speeds of mica powder and water-dispersible varnish are the same, the composition of the electrodeposition paint in the electrodeposition bath and the composition of the electrical insulation layer will be constant. We tried various methods to equalize the electrophoresis speed by making the specific resistance of the liquid and the water-dispersed varnish similar. As an example, when using a method of adjusting the liquid resistivity of a water-dispersed varnish using a dialysis tube or electrodialysis method, it is possible to remove miscellaneous ions in the water-dispersed varnish, so negative ions in the miscellaneous ions can be removed. Water does not migrate to the positive electrode, that is, the electrical conductor, and as a result, the water content of the electrical insulating layer decreases, and the mica powder is arranged densely and parallel to the surface of the electrical conductor, forming a mechanical structure in the electrical insulating layer. It was found that the strength of the target could be improved. However, in the dialysis tube method or electrodialysis method, it takes a long time to adjust the liquid specific resistance of the water-dispersed varnish and remove miscellaneous ions, and when a dialysis tube is used, a so-called batch method is used to process a large amount of water-dispersed varnish. The disadvantages are that it requires a lot of manpower to do this, and that the dialysis tube itself is difficult to use continuously due to its strength. The present inventors have discovered a method using ultrafiltration or reverse osmosis as a method capable of adjusting the liquid resistivity of a large amount of water-dispersed varnish and removing miscellaneous ions in a short time and continuously. In other words, the present invention aims to adjust the liquid resistivity of the water-dispersed varnish and to adjust the liquid specific resistance of the water-dispersed varnish before dispersing the mica powder and the water-dispersed varnish in order to equalize the electrophoresis speed of the mica powder and the water-dispersed varnish. The present invention relates to a method for producing an electrodeposition paint, characterized in that the removal of is carried out by ultrafiltration or reverse osmosis treatment. The permeable membrane used in the ultrafiltration or reverse osmosis treatment in the present invention may be any known one. Further, the concentration of the water-dispersed varnish is suitably 5 to 30% by weight, and the liquid resistivity is suitably 1000 to 5000 Ωcm. Next, the method of the present invention will be explained based on the drawings.
FIG. 1 is a schematic diagram of a processing apparatus for adjusting the liquid resistivity and removing miscellaneous ions of a water-dispersed varnish used in the present invention. 1 is a tank for storing the water-dispersible varnish, 2 is the water-dispersible varnish, 3 is piping for the water-dispersible varnish, 4a is a pump for flowing the water-dispersible varnish, and 4b is the recycled permeate that is returned to tank 1. 5a is a valve for adjusting the flow rate and pressure of the water-dispersed varnish flowing into the permeable membrane; 5b is a valve for adjusting the flow rate and pressure of the water-dispersed varnish flowing out from the permeable membrane; 6a is a valve for adjusting the flow rate and pressure of the water-dispersed varnish flowing out from the permeable membrane; A pressure gauge, 6b is a pressure gauge at the outlet of the permeable membrane, 7 is a permeable membrane, 8 is an ion exchange resin for regenerating permeated water, 9 is a flow of permeated liquid,
10 is a tank for storing the regenerated permeate, and 11 is the regenerated permeate. A water-dispersed varnish and ion-exchanged water are put in a tank 1 of this treatment device, and the water-dispersed varnish diluted with ion-exchanged water is sent to a permeable membrane 7 by a pump 4a, and the permeated liquid is separated into a concentrated liquid and a permeated liquid by the permeable membrane 7. separated. The concentrated water-dispersible varnish is returned to tank 1, while the permeate is regenerated with ion exchange resin 8 and enters tank 10. Recycled permeate water 11 from tank 10
is returned to tank 1 by pump 4b. By repeating this several times, the liquid specific resistance of the water-dispersed varnish can be adjusted and miscellaneous ions can be removed. Next, the water-dispersed varnish used in the present invention is prepared by adding an acid-added epoxy resin with an acid value of 30 to 60 from, for example, 100 parts of Epicote 1001 (an epoxy resin manufactured by Ciel Chemical Co., Ltd.), 25 parts of tetrahydrophthalic anhydride, and 6 parts of ethylene glycol. It can be obtained by dispersing this resin in warm water containing ammonia and then blowing nitrogen gas into it. Next, the method of the present invention will be explained with reference to Examples and Comparative Examples. In the Examples and Comparative Examples below, a liquid having a pH of 7.0, a nonvolatile content of 8.0%, and a liquid specific resistance of 250 Ωcm was used. Example 1 Water-dispersed varnish 30 and ion-exchanged water 30 of 5 MΩcm or more were placed in tank 1 and passed through the permeable membrane at a flow rate of approximately 12/min, and the concentrated liquid was returned to tank 1 at a flow rate of approximately 2/10 min. After repeating the process of returning the permeated liquid to tank 1 at a rate of about 10 per hour about 6 times, the process of returning the permeated liquid to tank 1 was stopped, and the excess ion-exchanged water was allowed to permeate. , PH7.0 after 9 hours, non-volatile content 7.90%, liquid specific resistance 2000Ωcm
A water-dispersible varnish was obtained. To 20 parts of the solid content of this water-dispersible varnish, 80 parts of mica powder of 35 mesh pass, which has been thoroughly washed with ion-exchanged water, is mixed, and ion-exchanged water is added and stirred well, resulting in a uniformly dispersed non-volatile content of 15%. An electrodeposition paint was prepared. A hexagonal-shaped coil previously formed in this electrodeposition paint was immersed, and a DC voltage of 100 V was applied for 20 seconds between the poles and a counter electrode with a distance of 50 cm to form an electrodeposited insulating layer on the coil. Table 1 shows the results of examining the film layers and composition of the formed insulating layer. Example 2 Solid content of water-dispersed varnish prepared in Example 1: 30
An insulating layer was formed on the coil in the same manner as in Example 1, except that 70 parts of mica powder and 70 parts of mica powder were used. Table 1 shows the thickness and composition of the obtained insulating layer. Example 3 Solid content of water-dispersed varnish prepared in Example 1: 10
An insulating layer was formed in the same manner as in Example 1, except that 90 parts of mica powder and 90 parts of mica powder were used. Table 1 shows the thickness and composition of the obtained insulating layer. Comparative Example 1 The water-dispersed varnish 30 having a pH of 7.0, a nonvolatile content of 8.0%, and a liquid specific resistance of 250 Ωcm was placed in several dialysis tubes (VISKING tubes manufactured by Shiraimatsu Kikai Co., Ltd.).
Add 10% of the water-dispersible varnish in a dialysis tube to 3 containers containing 30% of ion-exchanged water of 5MΩcm or more.
PH6.8, non-volatile content 7.5 after 96 hours
% and a water-dispersed varnish with a liquid specific resistance of 2000Ωcm. After mixing 80 parts of mica powder of 35 mesh pass thoroughly washed with ion-exchanged water to 20 parts of the solid content of this water-dispersible varnish, an insulating layer was formed on the coil in the same manner as in Example 1. Table 1 shows the thickness and composition of the obtained insulating layer. Comparative Example 2 Solid content of water-dispersed varnish prepared in Comparative Example 1: 10
After mixing 90 parts of mica powder of 35 mesh pass thoroughly washed with ion-exchanged water, Example 1
An insulating layer was formed on the coil using the same method. Table 1 shows the thickness and composition of the obtained insulating layer. 【table】

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

第1図は本発明に用いる水分散型ワニスの処理
装置の概略図である。 図面の符号、1:タンク、2:水分散型ワニ
ス、3:水分散型ワニスの流れ、4a,4b:ポ
ンプ、5a,5b:弁、6a,6b:圧力計、
7:透過膜、8:イオン交換樹脂、9:透過液の
流れ、10:タンク、11:再生透過液。
FIG. 1 is a schematic diagram of a water-dispersed varnish processing apparatus used in the present invention. Reference numbers in the drawings: 1: tank, 2: water-dispersed varnish, 3: flow of water-dispersed varnish, 4a, 4b: pump, 5a, 5b: valve, 6a, 6b: pressure gauge,
7: Permeable membrane, 8: Ion exchange resin, 9: Permeate flow, 10: Tank, 11: Regenerated permeate.

Claims (1)

【特許請求の範囲】 1 水分散型ワニスに限外過または逆浸透処理
を施して水分散型ワニスの液比抵抗を高めかつ水
分散型ワニス中の雑イオンを除去し、ついでこれ
とマイカ粉と水とを調合することを特徴とする電
着塗料の製造法。 2 前記水分散型ワニスがエポキシエステル系水
分散型ワニスであることを特徴とする特許請求の
範囲第1項記載の電着塗料の製造法。 3 前記水分散型ワニスの原液タンクと限外過
装置もしくは逆浸透処理装置の循環回路を形成
し、水分散型ワニスの一部を限外過もしくは逆
浸透処理を行なつて濃縮液と透過液に分離し、濃
縮液は原液タンクに戻し、透過液はイオン交換樹
脂により再生して原液タンクに戻すことにより、
水分散型ワニスが任意の液比抵抗になり、水分散
型ワニス中の雑イオンが除去できるまでこの操作
を繰り返すことを特徴とする特許請求の範囲第1
項記載の電着塗料の製造法。
[Claims] 1. Ultrafiltration or reverse osmosis treatment is applied to the water-dispersed varnish to increase the liquid specific resistance of the water-dispersed varnish and remove miscellaneous ions in the water-dispersed varnish, and then the water-dispersed varnish is treated with mica powder. A method for producing an electrodeposition paint, which comprises mixing the following: and water. 2. The method for producing an electrodeposition paint according to claim 1, wherein the water-dispersible varnish is an epoxy ester-based water-dispersible varnish. 3. A circulation circuit is formed between the stock solution tank of the water-dispersed varnish and an ultrafiltration device or a reverse osmosis treatment device, and a part of the water-dispersed varnish is subjected to ultrafiltration or reverse osmosis treatment to form a concentrated liquid and a permeated liquid. The concentrated liquid is returned to the stock solution tank, and the permeate is regenerated using an ion exchange resin and returned to the stock solution tank.
Claim 1, characterized in that this operation is repeated until the water-dispersed varnish reaches a desired liquid resistivity and miscellaneous ions in the water-dispersed varnish are removed.
Method for manufacturing the electrodeposition paint described in Section 1.
JP11427382A 1982-06-29 1982-06-29 Manufacture of electrodeposition coating Granted JPS594664A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11427382A JPS594664A (en) 1982-06-29 1982-06-29 Manufacture of electrodeposition coating

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11427382A JPS594664A (en) 1982-06-29 1982-06-29 Manufacture of electrodeposition coating

Publications (2)

Publication Number Publication Date
JPS594664A JPS594664A (en) 1984-01-11
JPH0224869B2 true JPH0224869B2 (en) 1990-05-30

Family

ID=14633686

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11427382A Granted JPS594664A (en) 1982-06-29 1982-06-29 Manufacture of electrodeposition coating

Country Status (1)

Country Link
JP (1) JPS594664A (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60159373U (en) * 1984-03-30 1985-10-23 横河電機株式会社 Electrolyte component measuring device with cleaning mechanism
JPH0668085B2 (en) * 1985-12-04 1994-08-31 三菱電線工業株式会社 Concentration method of water-dispersible varnish
JPH0695209B2 (en) * 1986-10-17 1994-11-24 東洋インキ製造株式会社 Plate making method
US5264902A (en) * 1990-02-07 1993-11-23 Canon Kabushiki Kaisha Image forming device
AT404434B (en) * 1997-06-12 1998-11-25 Frings Recycling Anlagen Gmbh METHOD FOR PROCESSING AN ELECTROLYTE USED FOR AN ELECTROPHORETIC PAINTING

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5189178A (en) * 1975-02-03 1976-08-04 ZETSUENTAINOSEI ZOHOHO
JPS5252878A (en) * 1975-10-28 1977-04-28 Kurita Water Ind Ltd Desalting apparatus using reverse osmotic membrane
JPS5952240B2 (en) * 1981-11-13 1984-12-18 旭化成株式会社 Ultrafiltration method

Also Published As

Publication number Publication date
JPS594664A (en) 1984-01-11

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