JPH0376770B2 - - Google Patents
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- Publication number
- JPH0376770B2 JPH0376770B2 JP1130070A JP13007089A JPH0376770B2 JP H0376770 B2 JPH0376770 B2 JP H0376770B2 JP 1130070 A JP1130070 A JP 1130070A JP 13007089 A JP13007089 A JP 13007089A JP H0376770 B2 JPH0376770 B2 JP H0376770B2
- Authority
- JP
- Japan
- Prior art keywords
- capacitance
- less
- dielectric
- ceramics
- weight
- 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
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- 239000003985 ceramic capacitor Substances 0.000 claims description 15
- VEALVRVVWBQVSL-UHFFFAOYSA-N strontium titanate Chemical compound [Sr+2].[O-][Ti]([O-])=O VEALVRVVWBQVSL-UHFFFAOYSA-N 0.000 claims description 14
- 238000010438 heat treatment Methods 0.000 claims description 8
- 230000006698 induction Effects 0.000 claims description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 7
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- 230000009467 reduction Effects 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 4
- 229910000416 bismuth oxide Inorganic materials 0.000 claims description 4
- TYIXMATWDRGMPF-UHFFFAOYSA-N dibismuth;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Bi+3].[Bi+3] TYIXMATWDRGMPF-UHFFFAOYSA-N 0.000 claims description 4
- 230000005684 electric field Effects 0.000 claims description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 4
- 239000000395 magnesium oxide Substances 0.000 claims description 4
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 3
- 230000000996 additive effect Effects 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 239000011651 chromium Substances 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 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 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 150000002739 metals Chemical class 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 229910052758 niobium Inorganic materials 0.000 claims description 3
- 239000010955 niobium Substances 0.000 claims description 3
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims description 3
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 239000000919 ceramic Substances 0.000 description 29
- 230000007423 decrease Effects 0.000 description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 3
- 229910002113 barium titanate Inorganic materials 0.000 description 3
- AOWKSNWVBZGMTJ-UHFFFAOYSA-N calcium titanate Chemical compound [Ca+2].[O-][Ti]([O-])=O AOWKSNWVBZGMTJ-UHFFFAOYSA-N 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000005611 electricity Effects 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 3
- 239000003990 capacitor Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229910052570 clay Inorganic materials 0.000 description 2
- 229910052839 forsterite Inorganic materials 0.000 description 2
- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000009958 sewing Methods 0.000 description 2
- -1 steatite Chemical compound 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Inorganic Insulating Materials (AREA)
- General Induction Heating (AREA)
- Control Of High-Frequency Heating Circuits (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Ceramic Capacitors (AREA)
Description
〔産業上の利用分野〕
本発明は、電源装置に関するもの、さらに詳し
くいえば、高周波の発振、共振または結合の電気
回路の部材にチタン酸ストロンチウム系セラミツ
クコンデンサを用いた電源装置に関するものであ
る。
〔従来の技術〕
木材、樹脂、塗料、食品、衣類などの高周波乾
燥や衣類の高周波ミシンなどの誘電加熱、あるい
は、鉄鋼の高周波焼入れ、金属、ガラスなどの高
周波熔融、または高周波熔融などの誘導加熱の用
途に対しては、その電源の回路に一部セラミツク
コンデンサが使用されている。
セラミツクコンデンサは、熱的、化学的に安定
である、小形化し得る等の他に、コンデンサの構
造が極めて簡単なため、高周波で使い易い。
通常、セラミツクコンデンサとしてはフオルス
テライト系、ステアタイト系、チタン酸マグネシ
ウム系、酸化チタン系、チタン酸カルシウム系な
どのセラミツクスが用いられているが、これらの
セラミツクスは誘電率が小さいためにある程度の
電源出力を確保する上にあつては電源装置が大形
化せざるを得ない。
近年、前記の各種用途の電源に関し、できるだ
け大出力化もしくは小形化が要望されて来てい
る。
この要望に応えるために、高誘電率の例えばチ
タン酸バリウム系のセラミツクスを誘電体とする
セラミツクスコンデンサを、前記各種用途の電源
の回路部材として使用することを検討して来た。
その結果は、従来の高誘電率系のセラミツクスで
は、使用中の温度上昇がはげしく、または課電時
の電源出力が計算通りにとれないなどの問題点が
あり、高周波の小電力の範囲に限定して使用せざ
るを得なかつた。本発明者らは、この原因は、こ
れら従来の高誘電率系のセラミツクスが強誘電性
であることによることを突き止め、これを常誘電
性又は程度の低い強誘電性のものに置き換えるこ
とによつてその問題点を克服しうることを見いだ
し、この知見に基づいて本発明をなすに至つた。
〔発明が解決しようとする課題〕
すなわち、本発明は、セラミツクコンデンサと
してチタン酸ストロンチウム系セラミツクスを用
いた、セラミツクコンデンサを前記回路の部材と
する高周波誘電または高周波誘導を用途とする電
源装置を提供するものである。本発明において、
チタン酸ストロンチウム系セラミツクスを用いた
ことにより上述した問題点である、使用中の温度
上昇を小さくするとともに、課電時の電源出力も
計算通りに近くとれ、さらに前記各種の電源の大
出力もしくは小形化を達成することができた。こ
れらについて、次に遂次、説明したい。
セラミツクコンデンサの使用中の温度上昇はセ
ラミツクスの高周波誘電体損失が小さいほど低く
押さえられる。これまでのフオルステライト系、
ステアタイト系、チタン酸マグネシウム系、酸化
チタン系、チタン酸カルシウム系などのセラミツ
クスの高周波誘電体損失は何れも0.1%以下のも
のが上記各種用途の電源の回路部材として実用化
されている。一方、電源の大出力化もしくは小形
化のためにはセラミツクスは誘電率が高いことが
必要であるが、この高誘電率系セラミツクスの中
で高周波誘電損失を0.1%以下のもので上記各種
セラミツクス並みのものを見い出すことはむずか
しく、現状では前述したように従来の高周波誘電
体損失が大きい高誘電率系のセラミツクスを使用
する限定した高周波の小電力の範囲に留まざるを
得ない。一方、本発明者らは、これまでチタン酸
ストロンチウム系セラミツクスを研究して来た
が、このセラミツクスが最近ではその高周波誘電
体損失が0.1%以下であるものが可能であり、こ
のセラミツクスを使用することによつて、はじめ
て上記各種用途の使用中の温度上昇を低く押える
ことに成功した。なお、このセラミツクスは、高
周波誘電体損失は、0.1%以下、また組成を適当
に選択すれば0.03%以下にまで小さくすることが
できる。また、高周波誘電体損失は、そのコンデ
ンサの使用寿命に大きく関係し、できるだけ小さ
いことがのぞましいので、この点でも有利であ
る。
次に、課電時の電源出力について説明したい。
上記各種用途の出力は使用するセラミツクコンデ
ンサに課電される電圧の自乗とその課電時の静電
容量の積に比例する。従つて、電源出力を大きく
するには、課電電圧を大きくすることがまず必要
である。しかるに、従来の高誘電率系セラミツク
スは課電時の静電容量が著しく低下するという欠
点があり、この欠点からも、従来の高誘電率系セ
ラミツクスを使用すると、限定した高周波の小電
力の範囲に留まらざるを得ない。近年、前記の各
種電源に関し、できるだけ電源出力の電圧を高く
することが要望され、回路設計の都合上、コンデ
ンサの能力の最上限まで電圧を印加することが、
しばしば必要とされるようになつたため、上記の
欠点の改善がこの分野の重要な課題となつてきて
いる。本発明者らは、この欠点の原因が、従来の
高誘電率系セラミツクスが強誘電性であることに
よるとみて、この場合も常誘電性または程度の低
い強誘電性のチタン酸ストロンチウム系セラミツ
クスであれば解決できることを見い出した。すな
わち、これまでのフオルステライト系、ステアタ
イト系、チタン酸マグネシウム系、酸化チタン
系、チタン酸カルシウム系などのセラミツクス
は、課電時の静電容量の低下は無視できる程度で
あるが、本発明のチタン酸ストロンチウム系セラ
ミツクスの課電時の静電容量の低下、すなわち、
静電容量の電圧の電圧依存率は1KV/mm誘電体
厚さ当り1%以下に押えられ、遥かに大きい低下
率を示すチタン酸バリウム系などの高誘電率系セ
ラミツクスに比べ非常に優れていることが云え
る。
また、温度特性は、20℃における静電容量に対
する85℃における静電容量の減少率を20%以下に
することができ、さらに、誘電率(または静電容
量)の経時変化が殆どなく優れている。従来の例
えばチタン酸バリウム系などの高誘電率系のセラ
ミツクスはこの経時変化が甚だ大きく、上記各種
用途の回路部材として適していないことが良く分
る。
したがつて、本発明の電源装置においては、比
誘電率1050〜1310、誘電体損失0.1%以下、静電
容量の電圧依存率1KV/mm誘電体厚さの電界当
り1%以下を有し、かつ20℃における静電容量に
対する85℃における静電容量の減少率が20%以下
であるチタン酸ストロンチウム系セラミツクコン
デンサを用いるものである。
〔課題を解決するための手段〕
この発明は、チタン酸ストロンチウム62.4〜
72.3重量%と酸化ビスマス7.1〜11.9重量%と酸化
チタン20.2〜23.9重量%と酸化マグネシウム0.4〜
2.4重量%とから成り、かつマンガン、ニオブ、
クロム、ニツケル、コバルト及び鉄の中から選ば
れた金属の酸化物と粘土質物と希土類元素酸化物
の中から選ばれた少なくとも1種の添加成分を含
有し、比誘電率1050〜1310、誘電体損失0.1%以
下、静電容量の電圧依存率1KV/mm誘電体厚さ
の電界当り1%以下を有し、かつ20℃における静
電容量に対する85℃における静電容量の減少率が
20%以下であるチタン酸ストロンチウム系セラミ
ツクコンデンサを用いた誘電または誘導加熱用の
電源装置である。
〔作 用〕
本発明は比較的比誘電率が大きくても、高周波
誘電体損失が小さいため、使用中の温度上昇を少
なくすることができ、また課電時の静電容量の低
下が小さいものである。
〔実施例〕
次に実施例によつて、本発明をさらに詳細に説
明する。
第1表に示す重量比でチタン酸ストロンチウ
ム、酸化ビスマス、酸化チタン、酸化マグネシウ
ム及び必要な添加成分を混合し、適当量のバイン
ダーを加え、直径16.5mm、厚さ1mmの円板に加圧
成形したのち約1200℃で2時間焼成してセラミツ
クスを得た。添加成分中の希土類元素酸化物は、
誘電体損失をさらに少なくするために添加される
ものであり、例えば酸化セリウム、酸化ランタン
などが用いられる。この添加量は、通常0.01〜10
重量%の範囲内で選ばれる。
また、マンガン、ニオブ、クロム、ニツケル、
コバルト及び鉄の酸化物と粘度質物は、ち密な組
織の焼結体を形成させるために鉱化剤として添加
されるものでありその添加量は、通常0.1〜0.5重
量%の範囲内で選ばれる。
これらのセラミツクスは、例えば第1図、第2
図に示す構造のセラミツクコンデンサとして使用
される。第1図においてセラミツクス1の両面に
はそれぞれ端子2,2′が電極3,3′を介しては
んだ付等の手段で固着され、その周囲全面にわた
つてエポキシ樹脂等の合成樹脂5で被覆されてい
る。4は連結具である。
第1図に示す形状のセラミツクコンデンサに加
工し、その特性を測定し、その結果を第1表に示
す。
[Industrial Application Field] The present invention relates to a power supply device, and more specifically, to a power supply device using a strontium titanate ceramic capacitor as a member of a high-frequency oscillation, resonance, or coupling electric circuit. [Prior art] Dielectric heating for high frequency drying of wood, resin, paint, food, clothing, etc., high frequency sewing machines for clothing, induction heating for induction hardening of steel, high frequency melting of metals, glass, etc. Ceramic capacitors are used in some of the power supply circuits for these applications. Ceramic capacitors are thermally and chemically stable, can be miniaturized, and have an extremely simple structure, making them easy to use at high frequencies. Normally, ceramic capacitors use ceramics such as forsterite, steatite, magnesium titanate, titanium oxide, and calcium titanate, but these ceramics have a low dielectric constant, so they can be used as a power source to some extent. In order to secure the output, the power supply device has to be larger. In recent years, there has been a demand for power supplies for the various uses mentioned above to be as large in output as possible or as compact as possible. In order to meet this demand, studies have been conducted on the use of ceramic capacitors whose dielectric material is barium titanate-based ceramics having a high dielectric constant, for example, as circuit members for power sources for the various uses mentioned above.
As a result, conventional high-permittivity ceramics have problems such as rapid temperature rise during use or inability to obtain the calculated power output when energized, and are limited to high-frequency, low-power ranges. I had no choice but to use it. The present inventors discovered that the cause of this is that these conventional high dielectric constant ceramics are ferroelectric, and by replacing them with paraelectric or less ferroelectric materials. The inventors have discovered that this problem can be overcome, and based on this knowledge, the present invention has been completed. [Problems to be Solved by the Invention] That is, the present invention provides a power supply device using strontium titanate-based ceramics as a ceramic capacitor and using the ceramic capacitor as a member of the circuit for high-frequency dielectric or high-frequency induction. It is something. In the present invention,
By using strontium titanate-based ceramics, the temperature rise during use, which is the problem mentioned above, can be reduced, and the power output when applying electricity can be obtained close to the calculated value. was able to achieve this goal. I would like to explain these in turn. The temperature rise during use of a ceramic capacitor can be suppressed as the high frequency dielectric loss of the ceramic is small. Previous forsterite series,
Ceramics such as steatite-based, magnesium titanate-based, titanium oxide-based, and calcium titanate-based ceramics with a high frequency dielectric loss of 0.1% or less have been put into practical use as circuit members for power supplies for the various uses mentioned above. On the other hand, ceramics need to have a high dielectric constant in order to increase the output power or downsize the power supply. It is difficult to find one, and at present, as mentioned above, we have no choice but to limit ourselves to the limited high-frequency, low-power range using conventional high-permittivity ceramics with large high-frequency dielectric loss. On the other hand, the present inventors have been researching strontium titanate-based ceramics, and recently it has become possible to use this ceramic with a high-frequency dielectric loss of 0.1% or less. As a result, for the first time, we succeeded in suppressing the temperature rise during use in the various applications mentioned above. Note that the high frequency dielectric loss of this ceramic can be reduced to 0.1% or less, and if the composition is appropriately selected, to 0.03% or less. Furthermore, the high-frequency dielectric loss is greatly related to the service life of the capacitor, and it is desirable that the high-frequency dielectric loss be as small as possible, which is also advantageous. Next, I would like to explain the power output when charging.
The output for each of the above-mentioned applications is proportional to the product of the square of the voltage applied to the ceramic capacitor used and the capacitance at the time of application. Therefore, in order to increase the power output, it is first necessary to increase the applied voltage. However, conventional high-permittivity ceramics have the disadvantage of a significant decrease in capacitance when a voltage is applied, and due to this disadvantage, conventional high-permittivity ceramics are difficult to use in a limited high-frequency, low-power range. I have no choice but to stay. In recent years, there has been a demand for the power supply output voltage to be as high as possible for the various power supplies mentioned above, and for reasons of circuit design, it is difficult to apply voltage up to the maximum capacity of the capacitor.
The improvement of the above-mentioned shortcomings has become an important task in this field as it is often required. The present inventors believe that this drawback is due to the fact that conventional high dielectric constant ceramics are ferroelectric; I found that there is a solution. In other words, conventional ceramics such as forsterite-based, steatite-based, magnesium titanate-based, titanium oxide-based, and calcium titanate-based ceramics have a negligible decrease in capacitance when electricity is applied, but the present invention The decrease in capacitance of strontium titanate ceramics when energized, i.e.,
The voltage dependence rate of capacitance voltage is kept to less than 1% per 1KV/mm dielectric thickness, which is extremely superior to high dielectric constant ceramics such as barium titanate, which have a much larger reduction rate. I can say that. In addition, the temperature characteristics are excellent, with the reduction rate of capacitance at 85°C being less than 20% relative to the capacitance at 20°C, and in addition, there is almost no change in dielectric constant (or capacitance) over time. There is. It is clear that conventional high dielectric constant ceramics, such as barium titanate ceramics, undergo extremely large changes over time and are not suitable as circuit members for the various uses mentioned above. Therefore, the power supply device of the present invention has a dielectric constant of 1050 to 1310, a dielectric loss of 0.1% or less, and a capacitance voltage dependence rate of 1 KV/mm per electric field of 1 KV/mm dielectric thickness, In addition, a strontium titanate ceramic capacitor is used in which the capacitance at 85°C decreases by 20% or less relative to the capacitance at 20°C. [Means for Solving the Problems] This invention provides strontium titanate 62.4~
72.3% by weight, bismuth oxide 7.1~11.9% by weight, titanium oxide 20.2~23.9% by weight, and magnesium oxide 0.4~
2.4% by weight, and consists of manganese, niobium,
Contains at least one additive component selected from oxides of metals selected from chromium, nickel, cobalt, and iron, clay materials, and oxides of rare earth elements, and has a dielectric constant of 1050 to 1310. It has a loss of 0.1% or less, a voltage dependence of capacitance of 1% or less per electric field of 1KV/mm dielectric thickness, and a reduction rate of capacitance at 85℃ relative to capacitance at 20℃.
This is a power supply device for dielectric or induction heating using a strontium titanate ceramic capacitor with a strontium titanate content of 20% or less. [Function] Even though the present invention has a relatively large dielectric constant, the high-frequency dielectric loss is small, so the temperature rise during use can be reduced, and the capacitance decreases when electricity is applied. It is. [Example] Next, the present invention will be explained in more detail with reference to Examples. Strontium titanate, bismuth oxide, titanium oxide, magnesium oxide, and the necessary additives are mixed in the weight ratio shown in Table 1, an appropriate amount of binder is added, and the mixture is press-formed into a disc with a diameter of 16.5 mm and a thickness of 1 mm. After that, it was fired at about 1200°C for 2 hours to obtain ceramics. The rare earth element oxides in the additive components are
It is added to further reduce dielectric loss, and for example, cerium oxide, lanthanum oxide, etc. are used. This addition amount is usually 0.01 to 10
Selected within the range of weight %. Also, manganese, niobium, chromium, nickel,
Cobalt and iron oxides and clay substances are added as mineralizers to form a sintered body with a dense structure, and the amount added is usually selected within the range of 0.1 to 0.5% by weight. . These ceramics are, for example, shown in Figures 1 and 2.
It is used as a ceramic capacitor with the structure shown in the figure. In FIG. 1, terminals 2 and 2' are fixed to both sides of a ceramic 1 through electrodes 3 and 3' by means such as soldering, and the entire surrounding area is covered with a synthetic resin 5 such as epoxy resin. ing. 4 is a connector. A ceramic capacitor having the shape shown in FIG. 1 was processed and its characteristics were measured. The results are shown in Table 1.
本発明に係る電源装置はセラミツクコンデンサ
としてチタン酸ストロンチウム、酸化ビスマス、
酸化チタン、酸化マグネシウムからなるチタン酸
ストロンチウム系セラミツクスを用い、比誘電率
1050〜1310、誘電体損失0.1%以下、静電容量の
電圧依存率1KV/mm誘電体厚さの電界当り1%
以下を有し、かつ20℃における静電容量に対する
85℃における静電容量の減少率が20%以下のセラ
ミツクスを用いた電源装置を特徴をとする為に、
高周波感応や高周波ミシン等の誘導加熱あるいは
高周波波焼入れ、高周波熔融、高周波熔接等の誘
導加熱用の電源装置として、電源の大出力化及び
小形化が可能となつたもので工業上の利益に多大
なものがある。
The power supply device according to the present invention uses strontium titanate, bismuth oxide,
Using strontium titanate ceramics consisting of titanium oxide and magnesium oxide, the relative dielectric constant is
1050~1310, dielectric loss 0.1% or less, voltage dependence of capacitance 1% per electric field of 1KV/mm dielectric thickness
with the following and for capacitance at 20℃
In order to feature a power supply device using ceramics with a capacitance reduction rate of 20% or less at 85℃,
As a power supply device for induction heating such as high-frequency sensing and high-frequency sewing machines, induction heating for high-frequency hardening, high-frequency melting, high-frequency welding, etc., it has become possible to increase the power output and downsize the power supply, and it has great industrial benefits. There is something.
第1図及び第2図は従来及び本発明に使用され
る高周波誘電加熱、誘導加熱用セラミツクコンデ
ンサの断面図を示す。第3図は本発明の実施例で
印加電圧に対する電圧依存率の関係を示す図であ
る。第4図は同じく本発明の実施例で温度に対す
る静電容量変化りつ示す図である。第5図は同じ
く本発明の実施例で静電容量の経時変化を示す図
である。
FIGS. 1 and 2 show cross-sectional views of ceramic capacitors for high frequency dielectric heating and induction heating used conventionally and in the present invention. FIG. 3 is a diagram showing the relationship of the voltage dependence rate to the applied voltage in an embodiment of the present invention. FIG. 4 is a diagram showing the change in capacitance with respect to temperature in the same embodiment of the present invention. FIG. 5 is a diagram showing the change in capacitance over time in the same example of the present invention.
Claims (1)
酸化ビスマス7.1〜11.9重量%と酸化チタン20.2〜
23.9重量%と酸化マグネシウム0.4〜2.4重量%と
から成り、かつマンガン、ニオブ、クロム、ニツ
ケル、コバルト及び鉄の中から選ばれた金属の酸
化物と粘土質物と希土類元素酸化物の中から選ば
れた少なくとも1種の添加成分を含有し、比誘電
率1050〜1310、誘電体損失0.1%以下、静電容量
の電圧依存率1KV/mm誘電体厚さの電界当り1
%以下を有し、かつ20℃における静電容量に対す
る85℃における静電容量の減少率が20%以下であ
るチタン酸ストロンチウム系セラミツクコンデン
サを用いた誘電または誘導加熱用の電源装置。1 Strontium titanate 62.4~72.3% by weight, bismuth oxide 7.1~11.9% by weight, and titanium oxide 20.2~
23.9% by weight and 0.4-2.4% by weight of magnesium oxide, and selected from oxides of metals selected from manganese, niobium, chromium, nickel, cobalt and iron, argillaceous materials and oxides of rare earth elements. Contains at least one additive component, has a relative dielectric constant of 1050 to 1310, a dielectric loss of 0.1% or less, and a voltage dependence of capacitance of 1 KV/mm per electric field of dielectric thickness.
% or less, and a dielectric or induction heating power supply device using a strontium titanate ceramic capacitor, which has a capacitance reduction rate of 20% or less at 85°C relative to the capacitance at 20°C.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1130070A JPH0228304A (en) | 1989-05-25 | 1989-05-25 | Power supply |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1130070A JPH0228304A (en) | 1989-05-25 | 1989-05-25 | Power supply |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10645281A Division JPS589315A (en) | 1981-07-08 | 1981-07-08 | Power source |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0228304A JPH0228304A (en) | 1990-01-30 |
| JPH0376770B2 true JPH0376770B2 (en) | 1991-12-06 |
Family
ID=15025279
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1130070A Granted JPH0228304A (en) | 1989-05-25 | 1989-05-25 | Power supply |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0228304A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102061508B1 (en) * | 2013-09-05 | 2020-01-02 | 삼성전기주식회사 | Dielectric ceramic composition and multilayer ceramic capacitor comprising the same |
| JP2015137194A (en) * | 2014-01-21 | 2015-07-30 | エプコス アクチエンゲゼルシャフトEpcos Ag | Dielectric ceramic composition, dielectric element, electronic component and laminated electronic component |
-
1989
- 1989-05-25 JP JP1130070A patent/JPH0228304A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0228304A (en) | 1990-01-30 |
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