JPH02180401A - Ceramic resonator and manufacture thereof - Google Patents
Ceramic resonator and manufacture thereofInfo
- Publication number
- JPH02180401A JPH02180401A JP33335488A JP33335488A JPH02180401A JP H02180401 A JPH02180401 A JP H02180401A JP 33335488 A JP33335488 A JP 33335488A JP 33335488 A JP33335488 A JP 33335488A JP H02180401 A JPH02180401 A JP H02180401A
- Authority
- JP
- Japan
- Prior art keywords
- sintered body
- electrode layer
- noble metal
- ceramic sintered
- cylindrical
- 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.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000000919 ceramic Substances 0.000 title abstract description 13
- 238000000034 method Methods 0.000 claims abstract description 9
- 229910000510 noble metal Inorganic materials 0.000 claims abstract description 9
- 238000007747 plating Methods 0.000 claims abstract description 9
- 239000003054 catalyst Substances 0.000 claims description 19
- 239000011882 ultra-fine particle Substances 0.000 claims description 11
- 239000002245 particle Substances 0.000 claims description 9
- 229910000831 Steel Inorganic materials 0.000 claims description 7
- 239000010959 steel Substances 0.000 claims description 7
- 239000010970 precious metal Substances 0.000 claims description 5
- 239000006185 dispersion Substances 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- 239000002923 metal particle Substances 0.000 claims 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract description 5
- 229910052802 copper Inorganic materials 0.000 abstract description 5
- 239000010949 copper Substances 0.000 abstract description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 abstract description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract description 4
- 230000003197 catalytic effect Effects 0.000 abstract description 3
- 239000007772 electrode material Substances 0.000 abstract description 3
- 239000010953 base metal Substances 0.000 abstract description 2
- -1 copper complex salt Chemical class 0.000 abstract description 2
- 229910052751 metal Inorganic materials 0.000 abstract description 2
- 239000002184 metal Substances 0.000 abstract description 2
- 238000005498 polishing Methods 0.000 abstract description 2
- 239000003513 alkali Substances 0.000 abstract 1
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 13
- 229910052763 palladium Inorganic materials 0.000 description 7
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 229910052709 silver Inorganic materials 0.000 description 5
- 239000004332 silver Substances 0.000 description 5
- 238000007772 electroless plating Methods 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000002093 peripheral effect Effects 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 2
- 229910002113 barium titanate Inorganic materials 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002940 palladium Chemical class 0.000 description 1
- HIJDQYZZPATXAO-UHFFFAOYSA-N palladium hydrochloride Chemical compound Cl.[Pd] HIJDQYZZPATXAO-UHFFFAOYSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
Landscapes
- Control Of Motors That Do Not Use Commutators (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は高周波用のセツミック共振器とその製造方法に
関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a high frequency electrostatic resonator and a manufacturing method thereof.
従来の技術
近年、情報通信機器の進展にともなって高周波用共振器
の需要は著しく増加しており、それとともに共振器の小
型化、高性能化や低価格化へのニーズが高まっている。BACKGROUND OF THE INVENTION In recent years, with the advancement of information and communication equipment, the demand for high-frequency resonators has increased significantly, and along with this, the need for smaller resonators, higher performance, and lower prices has also increased.
従来のセツミック共振器は第3図に示すようなものであ
り、第3図において1は強誘電性で筒状のセツミック焼
結体、2は貫通孔、3は電極層である。A conventional cetsmic resonator is as shown in FIG. 3, where 1 is a ferroelectric cylindrical cetsmic sintered body, 2 is a through hole, and 3 is an electrode layer.
このセツミック共振器は一般にチタン酸バリウムを主成
分とした強誘電性セツミックを任意の寸法を有する筒′
状に成型加工し、高温焼結して作ったセツミック焼結体
1の貫通孔2内周面および外周面の全面又は一部分を残
して選択的に銀粉末とガラスフリットを混合した導体ペ
ーストを塗布し、これを600〜800度の高温中で焼
成することによって電極層3を形成したものである。This cetsmic resonator is generally made of a ferroelectric cetsmic mainly composed of barium titanate, which is made of a cylinder with arbitrary dimensions.
A conductive paste containing a mixture of silver powder and glass frit is selectively applied to the entire or part of the inner and outer peripheral surfaces of the through hole 2 of the Cetsmic sintered body 1, which is formed by molding into a shape and sintering at high temperatures. The electrode layer 3 was formed by firing this at a high temperature of 600 to 800 degrees.
また一方、昨今セツミック共振器の低価格化や高性能化
を指向した電極形成法として、高温焼結した強誘電性の
セツミック焼結体に直接無電解鋼めっき法によって電極
層を形成する方法も行われている。On the other hand, recently, as an electrode formation method aimed at lowering the price and improving the performance of cetsmic resonators, there is also a method of directly forming an electrode layer on a ferroelectric cetsmic sintered body sintered at high temperature by electroless steel plating. It is being done.
発明が解決しようとする課題
しかしながら、上述したセツミック共振器では、前者の
銀とガラスの焼結体によって電極層3を形成したものは
、使用する電極材料が貴金属のため高価につくことはも
とより、セツミック焼結体1と銀導体の間にガラス層が
介在するだめ、高周波特性として特にQ特性が低下する
という問題があった。Problems to be Solved by the Invention However, in the above-mentioned cetsmic resonator, the former one in which the electrode layer 3 is formed of a sintered body of silver and glass is not only expensive because the electrode material used is a noble metal. Since the glass layer is interposed between the ceramic sintered body 1 and the silver conductor, there is a problem in that the high frequency characteristics, particularly the Q characteristics, are deteriorated.
さらに、銀ペーストラ筒状のセツミック焼結体1の貫通
孔2内周面や外周面に均一に塗布する方法が煩雑を極め
、量産性に欠けるという問題があった。Furthermore, the method for uniformly applying silver paste to the inner and outer peripheral surfaces of the through-holes 2 of the cylindrical sintered body 1 is extremely complicated, and there is a problem in that it lacks mass productivity.
また、後者の無電解めっき法によって強誘電性のセツミ
ック焼結体の表面に直接金属銅から成る電極層を形成し
たものは、無電解めっきの前処理として行う触媒付与処
理に錫とパラジウム塩酸酸性溶液から成る強酸性の触媒
液を使用するものである。しかし、強誘電性のセツミッ
ク焼結体にこのような触媒付与を行って無電解鋼めっき
をしたものは、塩酸性溶液によるセツミック焼結体の浸
食による機械的強度の劣化や、触媒層に錫が残存して触
媒活性が阻害され、めっきの付きまわシ性や密着性の劣
化による高周波特性、とりわけQ特性が低下するという
問題があった。In addition, in the case where an electrode layer made of metallic copper is directly formed on the surface of a ferroelectric ceramic sintered body by the latter electroless plating method, tin and palladium hydrochloric acid are used in the catalyst application treatment performed as a pretreatment for electroless plating. A strongly acidic catalyst solution consisting of a solution is used. However, when a ferroelectric ceramic sintered body is coated with such a catalyst and electroless steel plated, the mechanical strength deteriorates due to erosion of the ceramic sintered body by a hydrochloric acid solution, and tin is added to the catalyst layer. remains, inhibiting the catalytic activity, and deteriorating the coverage and adhesion of the plating, resulting in a decline in high frequency characteristics, especially Q characteristics.
本発明は上記のような問題点を解決し、記法性と高周波
特性にすぐれたセツミック共振器とその製造方法を提供
することを目的とするものである。It is an object of the present invention to solve the above-mentioned problems and to provide a static resonator with excellent notation and high frequency characteristics, and a method for manufacturing the same.
課題を解決するだめの手段
上記目的を達成するために本発明は強誘電性を有する筒
状のセツミック焼結体の表面に、貴金属超微粒子ゾルか
ら成る触媒層を介して無電解鋼めっきによる電極層を形
成したものである。Means for Solving the Problems In order to achieve the above objects, the present invention provides an electrode formed by electroless steel plating on the surface of a ferroelectric cylindrical setumic sintered body, with a catalyst layer made of ultrafine precious metal particle sol interposed therebetween. It is made up of layers.
作用
これにより、貴金属超微粒子ゾルから成る触媒層に錫が
残存することなく、均一かつ強固にセラミンク焼結体に
触媒層が付着するので、無電解めっきにより析出した電
極層の均一付着性が改善され、高周波特性にすぐれたセ
ツミック共振器が実現されることとなる。As a result, the catalyst layer is uniformly and firmly adhered to the ceramic sintered body without any tin remaining in the catalyst layer made of ultrafine precious metal particle sol, improving the uniform adhesion of the electrode layer deposited by electroless plating. As a result, a setmic resonator with excellent high frequency characteristics was realized.
実施例
以下、本発明の一実施例について図面を参照しながら説
明する。EXAMPLE Hereinafter, an example of the present invention will be described with reference to the drawings.
第1図は本発明の第一の実施例におけるセツミック共振
器の斜視図、第2図a及びbはセツミック共振器の製造
工程を説明するための断面図である。第1図および第2
図において、4は強誘電性で筒状のセツミック焼結体、
6はその貫通孔、6は貴金属超微粒子ゾルよりなる触媒
層、7は電極層である。FIG. 1 is a perspective view of a cetsmic resonator according to a first embodiment of the present invention, and FIGS. 2a and 2b are cross-sectional views for explaining the manufacturing process of the cetsmic resonator. Figures 1 and 2
In the figure, 4 is a ferroelectric cylindrical setumic sintered body;
6 is the through hole thereof, 6 is a catalyst layer made of noble metal ultrafine particle sol, and 7 is an electrode layer.
以上の構成から成るセツミック共振器について以下にそ
の製造工程の詳細を説明する。The details of the manufacturing process for the static resonator having the above configuration will be explained below.
本発明の第一の実施例では、チタン酸バリウムを主成分
とした強誘電性セツミックの生シロートを外径約6 m
、内径的2 m +高さ約8gの円筒状に成型加工し
、この円筒状成型体を120O〜1300℃の高温中で
焼成することによって、第1図に示すような円筒状のセ
ツミック焼結体4全作った。In the first embodiment of the present invention, a raw ferroelectric cetsumic material containing barium titanate as a main component was prepared with an outer diameter of approximately 6 m.
By molding into a cylinder with an inner diameter of 2 m and a height of approximately 8 g, and firing this cylindrical molded body at a high temperature of 120 to 1300 °C, a cylindrical setumic sintered product as shown in Fig. 1 is produced. I made all 4 bodies.
そして、このセツミック焼結体4にバレル研摩等を行っ
て素子の端部に丸みをもたせると共に、さらにフッ酸溶
液中でエツチング処理を行ってセツミック焼結体4の全
表面を粗面化した。Then, this ceramic sintered body 4 was subjected to barrel polishing or the like to round the edges of the element, and further etched in a hydrofluoric acid solution to roughen the entire surface of the ceramic sintered body 4.
次いで、第2図乙に示すようにこの円筒状のセツミック
焼結体4を貴金属超微粒子ゾルから成る触媒液に浸漬し
て貫通孔6の内周面及び外周面の全面又は必要によりレ
ジストを塗布して選択的に触媒層6を付着した。Next, as shown in FIG. 2B, this cylindrical ceramic sintered body 4 is immersed in a catalyst liquid consisting of precious metal ultrafine particle sol, and a resist is applied to the entire inner and outer peripheral surfaces of the through holes 6 or if necessary. Then, the catalyst layer 6 was selectively deposited.
この場合、貴金属超微粒子ゾルから成る触媒液としては
銀、パラジウム、白金等の単一金属から成る超微粒子ゾ
ルが使用できるが、本実施例ではパラジウムから成る超
微粒子ゾルを使用した。In this case, an ultrafine particle sol consisting of a single metal such as silver, palladium, or platinum can be used as the catalyst liquid consisting of a noble metal ultrafine particle sol, but in this example, an ultrafine particle sol consisting of palladium was used.
そしてこのパラジウム超微粒子ゾルは塩化ナトリウムと
共に水に溶解し、これに界面活性剤として陰イオン性の
ドデシルベンゼンスルフオン酸ナトリウムを加え、つづ
いて水素化はう素ナトリウムを滴下し還元を行って得た
平均粒径が30〜60人のパラジウム超微粒子から成る
ヒドロゾル系のものと、パラジウム超微粒子を水以外の
トルエンなどの有機溶剤中に分散したオルガノゾル系の
両者を使用した。This palladium ultrafine particle sol is dissolved in water together with sodium chloride, anionic sodium dodecylbenzenesulfonate is added as a surfactant, and then sodium borohydride is added dropwise for reduction. Both a hydrosol type consisting of ultrafine palladium particles having an average particle size of 30 to 60 particles and an organosol type consisting of ultrafine palladium particles dispersed in an organic solvent other than water such as toluene were used.
尚、これらの触媒液はいずれも化学的にほぼ中性の溶液
であるので、セツミック焼結体4を浸食することなく、
しかもパラジウム超微粒子の吸着性は極めて良好であシ
、セツミック焼結体4に均−且つ強固に触媒層6が形成
できる仁とがわかった。Incidentally, since all of these catalyst liquids are chemically almost neutral solutions, they do not erode the cetomic sintered body 4.
Furthermore, it was found that the adsorption properties of the ultrafine palladium particles were extremely good, and that the catalyst layer 6 could be formed evenly and firmly on the ceramic sintered body 4.
それから触媒処理を施したセツミック焼結体4は銅錯塩
のアルカリ溶液とホルマリンから成る無電解鋼めっき液
に浸漬し、第2図すに示すように貴金属超微粒子ゾルか
ら成る触媒層60表面に金属銅を6〜10μの厚さに析
出させ電極層7を形成した。Then, the catalytically treated CETSUMIC sintered body 4 is immersed in an electroless steel plating solution consisting of an alkaline solution of copper complex salt and formalin, and as shown in FIG. Electrode layer 7 was formed by depositing copper to a thickness of 6 to 10 microns.
この場合、パラジウム超微粒子ゾルから成る触媒層6に
よシセツミック焼結体40表面に均一性と密着性に優れ
た電極層7を形成することができた0
発明の効果
以上の説明から明らかなように本発明によるセツミック
共振器は、筒状の強誘電性セツミック焼結体の表面に貴
金属超微粒子ゾルからなる触媒層を介し無電解鋼めっき
法による電極層を形成したものである。In this case, it was possible to form an electrode layer 7 with excellent uniformity and adhesion on the surface of the sintered body 40 using the catalyst layer 6 made of palladium ultrafine particle sol. The cetsmic resonator according to the present invention has an electrode layer formed by electroless steel plating on the surface of a cylindrical ferroelectric cetsmic sintered body, with a catalyst layer made of ultrafine precious metal particle sol interposed therebetween.
従って、従来の銀電極のものに比べ電極材料の卑金属化
及び工程の簡略化による低コスト化がはかれると共に、
セツミック焼結体と電極層の間にガラス絶縁層が介在し
ないため高周波特性、とりわけQ特性が著しく向上する
利点の他に、従来の無電解めっき法に比べても貴金属超
微粒子ゾルの触媒効果によシセツミック焼結体への無電
解めっきのつきまわシ性や密着性が著しく改善される等
の効果が得られた。Therefore, compared to conventional silver electrodes, the electrode material is made from a base metal and the process is simplified, resulting in lower costs.
Since there is no glass insulating layer between the CETSUMIC sintered body and the electrode layer, the high frequency characteristics, especially the Q characteristics, are significantly improved. Effects such as a marked improvement in the spreadability and adhesion of electroless plating to a solid sintered body were obtained.
第1図は本発明の一実施例におけるセツミック共振器の
斜視図、第2図&とbは本発明の一実施例におけるセツ
ミック共振器の製造工程を説明するための断面図、第3
図は従来のセツミック共振器の断面図である。
4・・・・・・セツミック焼結体、6・川・・貫通孔、
6・・・・・・触媒層、7・・・・・・電極層。
代理人の氏名 弁理士 粟 野 重 孝 はが1名第1
図
t5ミヘソクfig体
第
図
6−m−触媒 層
7− 電ii&層
第
図
!FIG. 1 is a perspective view of a cetsmic resonator according to an embodiment of the present invention, FIGS.
The figure is a cross-sectional view of a conventional cetsmic resonator. 4...Setsumic sintered body, 6. River...through hole,
6... Catalyst layer, 7... Electrode layer. Name of agent: Patent attorney Shigetaka Awano (1 person)
Figure t5 Mihye Seok fig body Figure 6-M-Catalyst layer 7-Electric II & layer diagram!
Claims (4)
に貴金属超微粒子ゾルから成る触媒層を介して無電解鋼
めっきによる電極層を形成したことを特徴とするセツミ
ック共振器。(1) A CETSMIC resonator characterized in that an electrode layer made of electroless steel plating is formed on the surface of a ferroelectric cylindrical CETSMIC sintered body through a catalyst layer made of ultrafine noble metal particle sol.
に、貴金属超微粒子ゾルから成る触媒層を付与し、無電
解鋼めっき法により電極層を形成することを特徴とした
セツミック共振器 の製造方法。(2) A CETSUMIC resonator characterized in that a catalyst layer made of ultrafine precious metal particle sol is applied to the surface of a cylindrical CETSUMIC sintered body having ferroelectric properties, and an electrode layer is formed by electroless steel plating. manufacturing method.
子分散溶媒を使用した特許請求の範囲第2項に記載のセ
ツミック共振器の製造方法。(3) The method for manufacturing a cetmic resonator according to claim 2, in which a hydrosol-based ultrafine particle dispersion solvent is used as the noble metal ultrafine particle sol.
子分散溶媒を使用した特許請求の範囲第2項に記載のセ
ツミック共振器の製造方法。(4) The method for manufacturing a cetomic resonator according to claim 2, in which an organosol-based ultrafine particle dispersion solvent is used as the noble metal ultrafine particle sol.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33335488A JPH02180401A (en) | 1988-12-29 | 1988-12-29 | Ceramic resonator and manufacture thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33335488A JPH02180401A (en) | 1988-12-29 | 1988-12-29 | Ceramic resonator and manufacture thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02180401A true JPH02180401A (en) | 1990-07-13 |
Family
ID=18265173
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP33335488A Pending JPH02180401A (en) | 1988-12-29 | 1988-12-29 | Ceramic resonator and manufacture thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02180401A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20040036105A (en) * | 2002-10-23 | 2004-04-30 | 한국전기연구원 | Glass ceramic resonator for exciting laser using high efficiency reflector and manufacturing method thereof |
CN112913138A (en) * | 2018-10-26 | 2021-06-04 | Rf360欧洲有限责任公司 | Method for manufacturing an electroacoustic resonator and electroacoustic resonator device |
-
1988
- 1988-12-29 JP JP33335488A patent/JPH02180401A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20040036105A (en) * | 2002-10-23 | 2004-04-30 | 한국전기연구원 | Glass ceramic resonator for exciting laser using high efficiency reflector and manufacturing method thereof |
CN112913138A (en) * | 2018-10-26 | 2021-06-04 | Rf360欧洲有限责任公司 | Method for manufacturing an electroacoustic resonator and electroacoustic resonator device |
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