JPH04369909A - Crystal vibrator - Google Patents
Crystal vibratorInfo
- Publication number
- JPH04369909A JPH04369909A JP3173035A JP17303591A JPH04369909A JP H04369909 A JPH04369909 A JP H04369909A JP 3173035 A JP3173035 A JP 3173035A JP 17303591 A JP17303591 A JP 17303591A JP H04369909 A JPH04369909 A JP H04369909A
- Authority
- JP
- Japan
- Prior art keywords
- crystal
- conductive
- present
- polyhydric alcohol
- bisphenol
- 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
- 239000013078 crystal Substances 0.000 title claims abstract description 23
- 230000001070 adhesive effect Effects 0.000 claims abstract description 17
- 239000000853 adhesive Substances 0.000 claims abstract description 16
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims abstract description 8
- 239000000843 powder Substances 0.000 claims abstract description 8
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 7
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000004020 conductor Substances 0.000 claims abstract description 6
- 229920000642 polymer Polymers 0.000 claims abstract description 6
- 239000002184 metal Substances 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 229930185605 Bisphenol Natural products 0.000 claims description 3
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 abstract description 4
- 238000002156 mixing Methods 0.000 description 5
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 239000010453 quartz Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- -1 hydrogen compound Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
Landscapes
- Conductive Materials (AREA)
- Piezo-Electric Or Mechanical Vibrators, Or Delay Or Filter Circuits (AREA)
- Polyurethanes Or Polyureas (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、耐久性、接着性に優れ
、クラック発生のない水晶振動子に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a crystal resonator which has excellent durability and adhesive properties and is free from cracks.
【0002】0002
【従来の技術】水晶振動子は、水晶結晶体を所定の角度
に切断して形成した薄い水晶片に金属電極を設け、ケー
ス蓋板から延びる引出導体と金属電極とを接着した後、
水晶片にカバーを被せてこれを密封して製造され、発振
用等として広く使用されている。この水晶振動子の金属
電極と引出導体間あるいは半導体装置のパッドと引出導
体間等など導電性を保持させながら、両者間の機械的な
結合を維持させるため、導電性接着剤が使用されている
。従来は、この導電性接着剤として二液性のエポキシ系
接着剤が使用されていた。[Prior Art] A quartz resonator is manufactured by cutting a quartz crystal at a predetermined angle, providing metal electrodes on a thin quartz piece, and bonding the metal electrodes to a lead-out conductor extending from a case cover plate.
It is manufactured by covering a crystal piece with a cover and sealing it, and is widely used for oscillation purposes. Conductive adhesive is used between the metal electrode of this crystal resonator and the lead-out conductor, or between the pad of the semiconductor device and the lead-out conductor, etc., in order to maintain electrical conductivity and maintain mechanical bond between the two. . Conventionally, a two-component epoxy adhesive has been used as this conductive adhesive.
【0003】しかしながら、従来の導電性接着剤では満
足すべき特性が得られていない。例えば高周波用の薄型
水晶片を被覆している導電性接着剤が硬化後に水晶片に
クラックを発生させたり、水晶振動子の落下試験で発振
しないものが発生する等の欠点があった。また、二液性
のため二液混合後の可使時間が短いことや、アウトガス
(放出ガス)の発生量が多く、密着性を低下させ又は他
に影響を与えたりする欠点があった。However, conventional conductive adhesives do not have satisfactory properties. For example, there were drawbacks such as the conductive adhesive that coats a thin crystal piece for high frequency use causing cracks in the crystal piece after curing, and some crystal units failing to oscillate during a drop test. In addition, since it is a two-component product, it has short pot life after mixing the two-component products, and a large amount of outgas (released gas) is generated, which may reduce adhesion or affect other products.
【0004】0004
【発明が解決しようとする課題】本発明は、上記の欠点
を解消するためになされたもので、耐久性、接着性に優
れ、クラックの発生がなく、落下テストにおいても不発
振のない、アウトガスの発生量が少なく、可使時間の長
い水晶振動子を提供しようとするものである。[Problems to be Solved by the Invention] The present invention has been made in order to eliminate the above-mentioned drawbacks. The purpose is to provide a crystal resonator that generates a small amount of ion and has a long pot life.
【0005】[0005]
【課題を解決するための手段】本発明者は、上記の目的
を達成しようと鋭意研究を重ねた結果、後述する組成の
導電性接着剤を使用することによって、上記目的が達成
されることを見いだし、本発明を完成したものである。[Means for Solving the Problems] As a result of intensive research aimed at achieving the above object, the present inventor has found that the above object can be achieved by using a conductive adhesive having the composition described below. This discovery has led to the completion of the present invention.
【0006】即ち、本発明は、水晶片に設けられた金属
電極と引出導体とを、(A)ビスフェノールブロックウ
レタンポリマー、(B)多価アルコール化合物および(
C)導電性粉末下記を必須成分とする導電性接着剤で接
着固定してなることを特徴とする水晶振動子である。That is, the present invention provides metal electrodes and lead-out conductors provided on a crystal piece with (A) a bisphenol block urethane polymer, (B) a polyhydric alcohol compound, and (
C) Conductive powder A crystal resonator characterized by being adhesively fixed with a conductive adhesive containing the following essential components.
【0007】以下、本発明を詳細に説明する。The present invention will be explained in detail below.
【0008】本発明に用いる水晶片は、水晶結晶体を所
定の角度に切断した厚さ80μm 程度の薄片である。The crystal piece used in the present invention is a thin piece of about 80 μm thick obtained by cutting a crystal body at a predetermined angle.
【0009】本発明に用いる導電性接着剤は、(A)ビ
スフェノールブロックウレタンポリマー、(B)多価ア
ルコール化合物、(C)導電性粉末を含むものである。The conductive adhesive used in the present invention contains (A) a bisphenol block urethane polymer, (B) a polyhydric alcohol compound, and (C) a conductive powder.
【0010】本発明に用いる(A)ビスフェノールブロ
ックウレタンプレポリマーとしては、ウレタンを形成す
るプレポリマーおよびオリゴマーの末端活性イソシアネ
ート基を、ビスフェノール活性水素化合物でブロック化
したブロックイソシアネートプレポリマーである。代表
的なものとしては、末端活性イソシアネートを有するポ
リエステル又はポリブタジエンを、ビスフェノールAあ
るいはビスフェノールFでブロック化したものである。
これらは単独又は2 種以上混合して使用することがで
きる。これらのブロック化されたウレタンプレポリマー
およびオリゴマーは室温では安定であるが、120 ℃
以上に加熱するとイソシアネート基を解離する性質をも
っている。The bisphenol-blocked urethane prepolymer (A) used in the present invention is a blocked isocyanate prepolymer obtained by blocking the terminal active isocyanate groups of the urethane-forming prepolymer and oligomer with a bisphenol-active hydrogen compound. A typical example is one in which polyester or polybutadiene having a terminally active isocyanate is blocked with bisphenol A or bisphenol F. These can be used alone or in combination of two or more. These blocked urethane prepolymers and oligomers are stable at room temperature, but at 120 °C
It has the property of dissociating isocyanate groups when heated to a higher temperature.
【0011】本発明に用いる(B)多価アルコール化合
物としては、可撓性、柔軟性を考慮して長鎖のアルキル
基を有するもの、例えばポリエステル系、ポリブタジエ
ン系およびシリコーン系の多価アルコール化合物が使用
可能である。具体的には、出光石油化学社製R−45H
T、三洋化成社製ポリエチレングリコール,ポリプロピ
レングリコール、トーレシリコーン社製アルコール変性
シリコーンBYシリーズ等が挙げられ、これらは、単独
又は2 種以上混合して使用することができる。これら
の多価アルコール化合物の水酸基は前記のウレタンポリ
マーおよびオリゴマーから解離したイソシアネート基と
反応する。このウレタンポリマーやオリゴマーと多価ア
ルコール類の配合割合は、解離イソシアネート基(NC
O)と多価アルコール化合物の水酸基(OH)の比(N
CO/OH)が1.0〜 1.2当量の範囲であること
が望ましい。この配合割合が、1.0当量未満または
1.2当量を超えると所定の特性が得られず好ましくな
い。またこの反応系を促進する触媒としては、一般的に
はジアルキルチンジラウレート等が使用される。The polyhydric alcohol compound (B) used in the present invention is one having a long chain alkyl group in consideration of flexibility and softness, such as polyester-based, polybutadiene-based and silicone-based polyhydric alcohol compounds. is available. Specifically, R-45H manufactured by Idemitsu Petrochemical Co., Ltd.
T, polyethylene glycol, polypropylene glycol manufactured by Sanyo Chemical Co., Ltd., alcohol-modified silicone BY series manufactured by Toray Silicone Co., Ltd., etc., and these can be used alone or in combination of two or more types. The hydroxyl groups of these polyhydric alcohol compounds react with the isocyanate groups dissociated from the urethane polymers and oligomers. The blending ratio of this urethane polymer or oligomer and polyhydric alcohol is determined by dissociated isocyanate groups (NC
O) and the hydroxyl group (OH) of the polyhydric alcohol compound (N
CO/OH) is preferably in the range of 1.0 to 1.2 equivalents. This blending ratio is less than 1.0 equivalent or
If the amount exceeds 1.2 equivalents, the desired properties cannot be obtained, which is not preferable. Further, as a catalyst for promoting this reaction system, dialkyltin dilaurate or the like is generally used.
【0012】本発明に用いる(C)導電性粉末としては
、銀粉末、銅粉末、ニッケル粉末、表面に金属層を有す
る銀粉末等が挙げられ、これらは、単独又は2種以上混
合して使用することができる。これらの導電性粉末は、
いずれも平均粒径が10μm 以下であることが望まし
い。平均粒径が10μm を超えると、組成物の性状が
ペースト状にならず塗布性能が低下し好ましくない。導
電性粉末と樹脂成分との配合割合は、重量比で70/3
0〜90/10であることが望ましい。導電性粉末が、
70重量部未満であると満足な導電性が得られず、また
90重量部を超えると作業性や密着性が低下し好ましく
ない。[0012] Examples of the conductive powder (C) used in the present invention include silver powder, copper powder, nickel powder, and silver powder having a metal layer on the surface, and these may be used alone or in a mixture of two or more. can do. These conductive powders are
In both cases, it is desirable that the average particle diameter is 10 μm or less. If the average particle size exceeds 10 μm, the composition will not become paste-like and the coating performance will deteriorate, which is not preferable. The mixing ratio of conductive powder and resin component is 70/3 by weight.
It is desirable that it is 0 to 90/10. conductive powder,
If it is less than 70 parts by weight, satisfactory conductivity cannot be obtained, and if it exceeds 90 parts by weight, workability and adhesion will deteriorate, which is not preferable.
【0013】本発明に用いる導電性接着剤は、粘度調整
のため必要に応じて有機溶剤を使用することができる。
その溶剤類としては、ジオキサン、ヘキサン、酢酸セロ
ソルブ、エチルセロソルブ、ブチルセロソルブ、ブチル
セロソルブアセテート、ブチルカルビトールアセテート
、イソホロン等が挙げられ、これらは単独又は2 種以
上混合して使用することができる。また、本発明の目的
に反しない範囲に応じて、消泡剤、カップリング剤、そ
の他の添加剤を配合することができる。本発明に用いる
導電性接着剤の製造方法は、常法に従い各原料成分を十
分混合した後、更に例えば三本ロールによる混練処理を
し、その後、減圧脱泡して製造することができる。[0013] The conductive adhesive used in the present invention may contain an organic solvent if necessary to adjust the viscosity. Examples of the solvent include dioxane, hexane, cellosolve acetate, ethyl cellosolve, butyl cellosolve, butyl cellosolve acetate, butyl carbitol acetate, isophorone, etc., and these can be used alone or in combination of two or more. Further, an antifoaming agent, a coupling agent, and other additives may be blended within a range that does not contradict the purpose of the present invention. The conductive adhesive used in the present invention can be produced by thoroughly mixing each raw material component according to a conventional method, and then kneading the mixture using, for example, three rolls, followed by degassing under reduced pressure.
【0014】[0014]
【実施例】次に、本発明を実施例によって説明するが、
本発明はこれらの実施例によって限定されるものではな
い。実施例及び比較例において「部」とは特に説明が無
い限り「重量部」を意味する。[Examples] Next, the present invention will be explained by examples.
The present invention is not limited to these examples. In Examples and Comparative Examples, "parts" means "parts by weight" unless otherwise specified.
【0015】実施例1〜3
表1に示した各成分を三本ロールにより3 回混練して
一液性導電性接着剤(A)、(B)、(C)をそれぞれ
製造した。Examples 1 to 3 The components shown in Table 1 were kneaded three times using three rolls to produce one-component conductive adhesives (A), (B), and (C), respectively.
【0016】比較例
市販のエポキシ樹脂ベース溶剤型導電性接着剤(D)を
入手した。Comparative Example A commercially available epoxy resin-based solvent-type conductive adhesive (D) was obtained.
【0017】実施例1〜3及び比較例で得た導電性接着
剤(A)、(B)、(C)および(D)を厚さ80μm
の水晶片の電極部と半導体装置のパッド部に、ディス
ペンス塗布した後、150 ℃で30分間加熱硬化させ
てそれぞれ水晶振動子を製造した。30個の水晶振動子
について、水晶片クラックおよび75cm上法から10
回落下したときの不発振試料数を測定したので、その結
果を表1に示した。[0017] The conductive adhesives (A), (B), (C) and (D) obtained in Examples 1 to 3 and Comparative Examples were applied to a thickness of 80 μm.
A crystal resonator was manufactured by dispensing coating on the electrode part of the crystal piece and the pad part of the semiconductor device, and heating and curing it at 150° C. for 30 minutes. For 30 crystal resonators, crystal piece cracks and 10 from 75cm top method
The number of samples that failed to oscillate after being dropped twice was measured, and the results are shown in Table 1.
【0018】[0018]
【表1】[Table 1]
【0019】[0019]
【発明の効果】以上の説明及び表1からも明らかなよう
に本発明の水晶振動子は、耐久性、接着性に優れ、クラ
ックの発生がなく、また落下試験においても不発振がな
く、アウトガスの発生量も少なくて可使時間が長い、信
頼性の高いものである。Effects of the Invention As is clear from the above explanation and Table 1, the crystal resonator of the present invention has excellent durability and adhesion, does not generate cracks, does not oscillate in a drop test, and has no outgas. It is highly reliable, has a long pot life, and generates little amount of carbon dioxide.
Claims (1)
体とを、(A)ビスフェノールブロックウレタンポリマ
ー、(B)多価アルコール化合物および(C)導電性粉
末下記を必須成分とする導電性接着剤で接着固定してな
ることを特徴とする水晶振動子。Claim 1: The metal electrode provided on the crystal piece and the lead-out conductor are bonded together using a conductive adhesive containing (A) a bisphenol block urethane polymer, (B) a polyhydric alcohol compound, and (C) a conductive powder, the following being essential components: A crystal resonator characterized by being adhesively fixed with an adhesive.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3173035A JPH04369909A (en) | 1991-06-18 | 1991-06-18 | Crystal vibrator |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3173035A JPH04369909A (en) | 1991-06-18 | 1991-06-18 | Crystal vibrator |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04369909A true JPH04369909A (en) | 1992-12-22 |
Family
ID=15952996
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3173035A Pending JPH04369909A (en) | 1991-06-18 | 1991-06-18 | Crystal vibrator |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04369909A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6720713B2 (en) | 2000-06-14 | 2004-04-13 | Murata Manufacturing Co., Ltd. | Piezoelectric resonant component |
-
1991
- 1991-06-18 JP JP3173035A patent/JPH04369909A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6720713B2 (en) | 2000-06-14 | 2004-04-13 | Murata Manufacturing Co., Ltd. | Piezoelectric resonant component |
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