Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPS6048042B2 - Method for manufacturing a vibrating body for an acoustic transducer - Google Patents
[go: Go Back, main page]

JPS6048042B2 - Method for manufacturing a vibrating body for an acoustic transducer - Google Patents

Method for manufacturing a vibrating body for an acoustic transducer

Info

Publication number
JPS6048042B2
JPS6048042B2 JP12442476A JP12442476A JPS6048042B2 JP S6048042 B2 JPS6048042 B2 JP S6048042B2 JP 12442476 A JP12442476 A JP 12442476A JP 12442476 A JP12442476 A JP 12442476A JP S6048042 B2 JPS6048042 B2 JP S6048042B2
Authority
JP
Japan
Prior art keywords
vibrating
acoustic transducer
boron
manufacturing
vibrating body
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
Application number
JP12442476A
Other languages
Japanese (ja)
Other versions
JPS5350703A (en
Inventor
庸弘 塚越
照夫 当摩
俊和 吉野
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.)
Pioneer Corp
Original Assignee
Pioneer Electronic 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 Pioneer Electronic Corp filed Critical Pioneer Electronic Corp
Priority to JP12442476A priority Critical patent/JPS6048042B2/en
Publication of JPS5350703A publication Critical patent/JPS5350703A/en
Publication of JPS6048042B2 publication Critical patent/JPS6048042B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Diaphragms For Electromechanical Transducers (AREA)

Description

【発明の詳細な説明】 本発明は音響変換器用振動体の製造方法に関・し、特に
振動体の基体とは異なつた性質を有する硼素材料を浸透
拡散させて、振動体材料のヤング率E)またはヤング率
Eと密度ρとの比を高めた高性能な音響変換器用振動体
の製造方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a vibrating body for an acoustic transducer, and in particular, the Young's modulus ) or a method of manufacturing a high-performance vibrating body for an acoustic transducer with a high ratio of Young's modulus E to density ρ.

従来上記したような振動体に使用されている材料として
は軽量で圧延加工容易なアルミニウム、チタン等が多く
用いられていたが、振動体が振動板の場合には、その材
料からして振動板全体に特定の振動モードが生じ、高域
の周波数特性に大きなピークを生じ著しく音質を害する
ものであり、レコードプレヤー・カートリッジ用カンチ
レバーの場合には、振動系の実効質料の大半をカンチレ
バーが占めてしまい、カートリッジの高性能化に必要な
振動系の実効質量を小さくすることが非常に困難であつ
た。
Conventionally, the materials used for the above-mentioned vibrating bodies are often aluminum, titanium, etc., which are lightweight and easy to roll. A specific vibration mode occurs throughout the vibration system, causing a large peak in the high frequency response, which significantly impairs sound quality.In the case of cantilevers for record player cartridges, the cantilever accounts for most of the effective mass of the vibration system. Therefore, it has been extremely difficult to reduce the effective mass of the vibration system, which is necessary to improve the performance of the cartridge.

すなわち、カンチレバーを軽量化しようとしてバイブの
肉厚、直径を減少していくと、剛性が低下して特性が悪
化してしまう欠点があつた。
That is, when the thickness and diameter of the vibrator are reduced in an attempt to reduce the weight of the cantilever, the rigidity decreases and the characteristics deteriorate.

上記特性を改良するにはヤング率Eと密度ρの比E/ρ
(以下比弾性率と称する)が大きな材料を使用すること
により行なうことができる。この比弾性率比E/ρの大
きな材料としては硼素、ベリリウム等がるが、硼素は入
手が困難であり(特に良質のもの)、ベリリウムは製造
工程において公害防止設備に多額の費用を必要とする。
また、硼素、ベリリウムは圧延やブレス等の加工が困難
であり、所定の形状に形成するには多額の費用を要する
とともに、その形状も大幅に制限されるものであつた。
そこで、アルミニウム、チタン等の成形加工容一易な材
料を、所定の形状に成形しておき、該成形物を基体とし
て、硼素、ベリリウム等を物理的蒸着あるいは化学的手
段によつてコーティングした振動板、カンチレバー等を
得ることが考えられる。
To improve the above characteristics, the ratio of Young's modulus E to density ρ is E/ρ.
This can be achieved by using a material with a large specific elastic modulus (hereinafter referred to as specific modulus). Materials with a large specific elastic modulus ratio E/ρ include boron, beryllium, etc., but boron is difficult to obtain (especially high quality ones), and beryllium requires a large amount of money for pollution prevention equipment in the manufacturing process. do.
Further, boron and beryllium are difficult to process by rolling, pressing, etc., and forming them into a predetermined shape requires a large amount of cost, and the shape is also severely limited.
Therefore, an easily molded material such as aluminum or titanium is molded into a predetermined shape, and the molded material is used as a base material and is coated with boron, beryllium, etc. by physical vapor deposition or chemical means. It is possible to obtain plates, cantilevers, etc.

ところで、物理的蒸着または化学的手段によ!り振動基
体にコーティング層を形成する場合、蒸着膜の特性を向
上させるには振動基体を150゜C以上に加熱すること
が望ましいが、この場合振動基体とコーティング層の熱
膨張係数が大きく異なるので、冷却後に機械的な歪が生
じたり、コーテイーング層に亀裂が生じて使用に耐えな
くなることがある。また蒸着等により振動基体にベリリ
ウムまたは硼素等のコーティング層を設け、このコーテ
ィング層のみを基体から剥離して、ベリリウムまたはク
硼素の振動体を形成することも提案されているが、蒸着
等の手段で製作されたベリリウムまたは硼素のコーティ
ング層は機械的強度が低く、壊れやすいという欠点を有
する。
By the way, by physical vapor deposition or chemical means! When forming a coating layer on a vibrating substrate, it is desirable to heat the vibrating substrate to 150°C or higher in order to improve the properties of the deposited film, but in this case, the thermal expansion coefficients of the vibrating substrate and the coating layer are significantly different. After cooling, mechanical distortion may occur or cracks may occur in the coating layer, making it unusable. It has also been proposed to provide a coating layer of beryllium or boron on the vibrating base by vapor deposition or the like, and to peel only this coating layer from the base to form a vibrating body of beryllium or boron. The beryllium or boron coating layer produced by Beryllium or Boron has the disadvantage of having low mechanical strength and being easily broken.

また蒸着等の手段]ーテイング層を振動基体上に形成す
るには、電子ビーム加熱等の蒸発装置が必要となり、設
備に多額の費用がかかる上、長い製作時間を要するため
、製品コストが非常に高くなる。そこで、振動基体に硼
素のコーティング層を形成し、これを熱処理することよ
つて基体に硼素の拡散した音響変換器用振動体が提案さ
れている。
In addition, in order to form a coating layer on a vibrating substrate by means such as vapor deposition, an evaporation device such as electron beam heating is required, which requires a large amount of equipment and a long production time, resulting in a very high product cost. It gets expensive. Therefore, a vibrating body for an acoustic transducer has been proposed in which boron is diffused in the base by forming a coating layer of boron on the vibrating base and heat-treating the coating layer.

しかしながら、この提案に係る音響変換器用振動体は、
振動基体に拡散層を形成することを特徴にlしているが
、この層を形成するに当つて、物理的蒸着あるいは化学
的手段を用いて振動基体に拡散層を生成する拡散物質の
コーティング層を形成するため、製造プロセスに非常に
多額の設備を必要とし、また拡散層になるコーティング
層が硼素のように非常に沸点が高い加工困難な材料にあ
つては、振動基体にコーティング層を形成する時間が長
くかかり、製造コストが高くつき、したがつて提供され
る音響変換器用振動体の製品コストが非常に高くなる欠
点があつた。また振動基体に拡散層を形成する熱処理温
度が非常に高く(振動基体にチタン、拡散材料に硼素を
それぞれ用いた場合9000C〜1300′C)、この
ため基体に機械的な歪が生じて変形したり、亀裂が生じ
たりし、この対策に苦慮しなければならない欠点が生じ
た。このような欠点に対する解決策として、化学気相析
出法によつて硼素層を振動基体に形成するという方法が
提案されている。
However, the vibrating body for an acoustic transducer according to this proposal is
It is characterized by forming a diffusion layer on the vibrating base, and in forming this layer, a coating layer of a diffusive substance is used to create the diffusion layer on the vibrating base using physical vapor deposition or chemical means. The manufacturing process requires a very large amount of equipment to form the diffusion layer, and if the coating layer that becomes the diffusion layer is made of a material such as boron that has a very high boiling point and is difficult to process, it is necessary to form the coating layer on the vibrating substrate. This has disadvantages in that it takes a long time to process and the manufacturing cost is high, resulting in a very high product cost of the vibrating body for an acoustic transducer. Furthermore, the heat treatment temperature for forming the diffusion layer on the vibrating base is extremely high (9000C to 1300'C when titanium is used for the vibrating base and boron is used as the diffusion material), which causes mechanical strain and deformation in the base. This resulted in problems such as cracks and cracks that had to be taken care of. As a solution to these drawbacks, a method has been proposed in which a boron layer is formed on the vibrating substrate by chemical vapor deposition.

この方法では、キャリアガスとして水素ガスを使用し、
塩化硼素ガス(BCe3)より硼素を析出させているが
、水素ガスを用いると、チタンと反応して、水素化チタ
ンが形成され、非常にもろくなつて振動体として使用不
能となる。本発明は叙上の如き欠点を克服するために成
されたもので、その主たる目的は、振動体になるべき振
動基体に拡散材料を被覆形成することなく、安価に大量
生産可能で特性のバラツキの少ない、基体に拡散材料を
浸透拡散させる有効な手段を提供することによつて振動
基体内に拡散材料の拡散領域を有する高性能な音響変換
器用振動体を得ることにある。
This method uses hydrogen gas as a carrier gas,
Boron is precipitated from boron chloride gas (BCe3), but when hydrogen gas is used, it reacts with titanium to form titanium hydride, making it extremely brittle and unusable as a vibrating body. The present invention was made to overcome the above-mentioned drawbacks, and its main purpose is to enable mass production at low cost without coating the vibrating base, which is to become a vibrating body, with a diffusion material, and to reduce the variation in characteristics. An object of the present invention is to obtain a high-performance vibrating body for an acoustic transducer having a diffusion region of a diffusive material in a vibrating base by providing an effective means for permeating and diffusing a diffusing material into a base with a small amount.

また本発明の他の目的は、振動体になるべき振動基体に
拡散材料の拡散領域を形成する際、振動基体に機械的な
歪が生じるために起きる変形、亀裂が生じることのない
音響変換器用振動体の製造方法を提供することにある。
Another object of the present invention is to provide an acoustic transducer that does not cause deformation or cracks caused by mechanical strain on the vibrating base when forming a diffusion region of a diffusion material on the vibrating base to become a vibrating body. An object of the present invention is to provide a method for manufacturing a vibrating body.

次に本発明の音響変換器用振動体の製造方法を図面とと
もに詳細に説明する。一般に、振動基体材料を加熱する
と非常に活性化され、還元性ガス雰囲気中でないと、表
面が酸化し、硼素層の形成が不可能とる。
Next, a method for manufacturing a vibrating body for an acoustic transducer according to the present invention will be explained in detail with reference to the drawings. Generally, when the vibrating base material is heated, it becomes highly activated, and unless it is in a reducing gas atmosphere, the surface will oxidize, making it impossible to form a boron layer.

そのために、キャリアガスとして水素ガスを使用するこ
とが考えられるが実際には前述の如き欠点のために使用
できない(特にチタンを基体とした場合)。そこで、本
発明の1つの特徴としては、キャリアガスに一酸化炭素
ガスを用いた点が挙げられる。図は本発明の方法に用い
る装置の一実施形態を示す構成図である。まず、それぞ
れの目的の音響変換器用振動体の形状に形成した振動基
体1を自動温度調節器2を備えた反応管3の中に適切に
設定する。振動基体材料としてはチタン、ジルコニウム
、イットリウム、バナジウム等の無機固体物質を使用す
ることができるが、本発明においては特にチタンを用い
た実施形態について説明する。このように設定した反応
管3内に原料ガス4およびキャリアガスとしての一炭酸
化炭素(CO)5をそれぞれ流量計6および6″によつ
て適切な混合比に混合して導入し、反応管に通電して基
体温度が900′C〜1200℃となるように加熱する
。原料ガスとして塩化硼素(BCf3)、臭化硼素(B
Br3)、ヨウ化硼素(BI3)、フッ化硼素(BF3
)等を用いることができるが、本発明においては、特に
塩化硼素(BC′3)を用いた場合について説明する。
このように、振動基体1を設定した反応管3に原料ガス
4とキャリアガス5との混合ガスを通じ、加熱して、チ
タン振動基体表面にコーティング層として析出した拡散
材料たる硼素が析出されると同時に振動基体内に浸透拡
散するうにして拡散層を形成する。上記拡散層は硼素と
チタンの金属間化合物を形成するが、このようにして形
成された金属間化合物は硼化チタン(TlB2)が主体
であり、硼化チタンのヤング率Eは58,000k9/
順2と非常に大きくなり、チタンのみの場合の約5倍に
も達する。硼化チタンの比重pは約3.8y/Ccてあ
るから比弾性率(E/ρ)は1.5×1010−となる
。これは硼素の比弾性率とほぼ同等の値である。これに
対して、チタン振動基体上に硼素層を設け、上記硼素層
とチタンの二重構造の振動体を製作した場合、見掛け上
のヤング率および密度はチタンと硼素のそれを合成した
ものとなり、比弾性率は硼素の値より必ず低くなり、硼
素拡散したものの比弾性率より劣ることになる。
For this reason, it is conceivable to use hydrogen gas as a carrier gas, but in practice this cannot be used due to the drawbacks mentioned above (particularly when titanium is used as the substrate). Therefore, one feature of the present invention is that carbon monoxide gas is used as the carrier gas. The figure is a configuration diagram showing one embodiment of an apparatus used in the method of the present invention. First, a vibrating base 1 formed in the shape of a vibrating body for an acoustic transducer for each purpose is appropriately set in a reaction tube 3 equipped with an automatic temperature controller 2. Although inorganic solid substances such as titanium, zirconium, yttrium, and vanadium can be used as the vibrating base material, an embodiment using titanium will be particularly described in the present invention. A raw material gas 4 and carbon monocarbonate (CO) 5 as a carrier gas are mixed at an appropriate mixing ratio and introduced into the reaction tube 3 set in this way using flowmeters 6 and 6'', respectively. The substrate is heated to a temperature of 900'C to 1200°C by applying electricity to the substrate.Boron chloride (BCf3) and boron bromide (B
Br3), boron iodide (BI3), boron fluoride (BF3)
), etc., but in the present invention, a case in which boron chloride (BC'3) is used will be explained in particular.
In this way, a mixed gas of raw material gas 4 and carrier gas 5 is passed through the reaction tube 3 in which the vibrating base 1 is set, and heated, and boron, which is a diffusion material, is deposited as a coating layer on the surface of the titanium vibrating base. At the same time, it permeates and diffuses into the vibrating base to form a diffusion layer. The above diffusion layer forms an intermetallic compound of boron and titanium, and the intermetallic compound thus formed is mainly titanium boride (TlB2), and the Young's modulus E of titanium boride is 58,000k9/
It is extremely large in rank 2, reaching about five times that in the case of titanium alone. Since the specific gravity p of titanium boride is approximately 3.8y/Cc, the specific elastic modulus (E/ρ) is 1.5×10 10 −. This value is approximately equivalent to the specific elastic modulus of boron. On the other hand, if a boron layer is provided on a titanium vibrating base and a double-structure vibrating body made of the boron layer and titanium is manufactured, the apparent Young's modulus and density will be a combination of those of titanium and boron. , the specific elastic modulus is always lower than the value of boron, and is inferior to the specific elastic modulus of a material with boron diffused therein.

従つて、塩化硼素(BCe3)ガスより析出した硼素を
殆んど全部チタン振動基体内に拡散させるという本発明
の方法による場合の方がより高性能な振動体が得られる
。このように、チタン振動基体表面に析出した硼素を殆
んど全部チタン振動基体内部に拡散させるためには、硼
素の析出速度を非常に遅くする必要があり、発明者の実
験においては、壱酸化炭素(CO)キャリアガスと塩化
硼素(BC′3)ガスの混合比を20:1とし、約2f
/Min.の流量で約2分間反応管(内径約60φ)に
流した時にほぼ上記の最適条件が得られた。なお、上記
実験においては、反応管の温度は基体温度が1000′
Cとなるよう選択した。上記の流量及び時間以下におい
ては、析出した硼素は殆んど全てチタン振動基体内に拡
散され、振動基体表面上には硼素層は形成されない。な
おコーティングされる拡散材料としては、硼素の外にシ
リコン、炭素などがあり、これ等は無機固体物質てある
Therefore, a vibrating body with higher performance can be obtained by using the method of the present invention in which almost all of the boron precipitated from boron chloride (BCe3) gas is diffused into the titanium vibrating base. In this way, in order to diffuse almost all of the boron deposited on the surface of the titanium vibrating base into the interior of the titanium vibrating base, it is necessary to make the precipitation rate of boron extremely slow. The mixing ratio of carbon (CO) carrier gas and boron chloride (BC'3) gas is 20:1, and approximately 2f
/Min. When the reaction tube was allowed to flow through the reaction tube (inner diameter of about 60φ) for about 2 minutes at a flow rate of In the above experiment, the temperature of the reaction tube was 1000'
I chose C. At a flow rate and time less than the above, almost all of the deposited boron is diffused into the titanium vibrating base, and no boron layer is formed on the surface of the vibrating base. In addition to boron, the diffusion materials to be coated include silicon, carbon, etc., which are inorganic solid substances.

上記のような本発明の音響変換器用振動体の製造方法に
よれば、還元性のキャリアガスとして一酸化炭素を用い
るために振動基体の酸化を防止することができるととも
に、チタンとキャリアガスとの反応を生じることがなく
、安定した硼素の析』出、沈積、従つて拡散を確保する
ことがてきる。
According to the method for manufacturing a vibrating body for an acoustic transducer of the present invention as described above, since carbon monoxide is used as a reducing carrier gas, oxidation of the vibrating base can be prevented, and the combination of titanium and carrier gas can be prevented. Stable boron precipitation, deposition, and therefore diffusion can be ensured without causing any reaction.

さらに、本発明の方法によれば、毒性の強い塩化硼素(
BC′3)ガスの使用量が少なくて済み、製作された振
動体は厚さがほんの僅か増加する程度で寸法の変化が小
さく、析出される硼素層の膜7厚のコントロールおよび
除去も不要であるため工程が簡単化され、バラツキが少
なくかつ高性能の音響変換器用振動体を得ることができ
る。
Furthermore, according to the method of the present invention, highly toxic boron chloride (
BC'3) The amount of gas used is small, the manufactured vibrating body has only a slight increase in thickness, and the change in dimensions is small, and there is no need to control or remove the thickness of the deposited boron layer. Therefore, the process is simplified, and a vibrating body for an acoustic transducer with little variation and high performance can be obtained.

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

図は本発明の音響変換器用振動体の製造方法に使用する
装置の一実施形態を示す構成図である。 1・・・・・・振動基体、3・・・・・・反応管、4・
・・・・・原料ガス、5・・・・・・一酸化炭素ガス。
The figure is a configuration diagram showing one embodiment of an apparatus used in the method of manufacturing a vibrating body for an acoustic transducer according to the present invention. 1... Vibrating base, 3... Reaction tube, 4...
... Raw material gas, 5 ... Carbon monoxide gas.

Claims (1)

【特許請求の範囲】 1 無機固体物質よりなり所望形状に形成された音響変
換器用振動体になるべき振動基体を用意する工程と、加
熱した上記振動基体に拡散材料である硼素を含む原料ガ
スとキャリアガスとしての一酸化炭素とを混合した混合
ガスを導く工程と上記混合ガス雰囲気中にて原料ガス中
の拡散材料を振動基体に析出させると共に析出した拡散
材料を振動基体に拡散させる工程とを具備し、拡散材料
が一定時間内に振動基体表面に析出する析出量より、拡
散材料が振動基体内部に拡散する拡散量を大とするよう
硼素を含む原料ガスの流量を制限したことを特徴とする
音響変換器用振動体の製造方法。 2 振動基体材料としてチタンまたはチタンを主成分と
するチタン含有物を用いたことを特徴とする前記特許請
求の範囲第1項の音響変換器用振動体の製造方法。 3 振動基体材料としてジルコニウムまたはジルコニウ
ムを主成分とするジルコニウム含有物を用いたことを特
徴とする前記特許請求の範囲第1項の音響変換器用振動
体の製造方法。 4 振動基体材料としてイットリウムまたはイットリウ
ムを主成分とするイットリウム含有物を用いたことを特
徴とする前記特許請求の範囲第1項の音響変換器用振動
体の製造方法。 5 振動基体材料としてバナジウムまたはバナジウムを
主成分とするバナジウム含有物を用いたことを特徴とす
る前記特許請求の範囲第1項の音響変換器用振動体の製
造方法。 6 原料ガスが塩化硼素(BCl_3)より成ることを
特徴とする前記特許請求の範囲第1項の音響変換器用振
動体の製造方法。 7 原料ガスが臭化硼素(BBr_3)より成ることを
特徴とする前記特許請求の範囲第1項の音響変換器用振
動体の製造方法。 8 原料ガスがヨウ化硼素(BI_3)より成ることを
特徴とする前記特許請求の範囲第1項の音響変換器用振
動体の製造方法。 9 原料ガスがフッ化硼素(BF_3)より成ることを
特徴とする前記特許請求の範囲第1項の音響変換器用振
動体の製造方法。
[Claims] 1. A step of preparing a vibrating base to be a vibrating body for an acoustic transducer made of an inorganic solid material and formed into a desired shape, and applying a raw material gas containing boron as a diffusion material to the heated vibrating base. A step of introducing a mixed gas mixed with carbon monoxide as a carrier gas, and a step of precipitating a diffusion material in the source gas onto a vibrating base in the mixed gas atmosphere and diffusing the precipitated diffusion material into the vibrating base. The flow rate of the source gas containing boron is restricted so that the amount of diffusion material diffused into the vibrating base is greater than the amount of diffusion material deposited on the surface of the vibrating base within a certain period of time. A method for manufacturing a vibrating body for an acoustic transducer. 2. The method for manufacturing a vibrating body for an acoustic transducer according to claim 1, characterized in that titanium or a titanium-containing material containing titanium as a main component is used as the vibrating base material. 3. The method for manufacturing a vibrating body for an acoustic transducer according to claim 1, characterized in that zirconium or a zirconium-containing material containing zirconium as a main component is used as the vibrating base material. 4. The method for manufacturing a vibrating body for an acoustic transducer according to claim 1, characterized in that yttrium or an yttrium-containing material containing yttrium as a main component is used as the vibrating base material. 5. The method for manufacturing a vibrating body for an acoustic transducer according to claim 1, characterized in that vanadium or a vanadium-containing material containing vanadium as a main component is used as the vibrating base material. 6. The method for manufacturing a vibrating body for an acoustic transducer according to claim 1, wherein the raw material gas is made of boron chloride (BCl_3). 7. The method for manufacturing a vibrating body for an acoustic transducer according to claim 1, wherein the raw material gas is made of boron bromide (BBr_3). 8. The method for manufacturing a vibrating body for an acoustic transducer according to claim 1, wherein the raw material gas is made of boron iodide (BI_3). 9. The method for manufacturing a vibrating body for an acoustic transducer according to claim 1, wherein the raw material gas is made of boron fluoride (BF_3).
JP12442476A 1976-10-19 1976-10-19 Method for manufacturing a vibrating body for an acoustic transducer Expired JPS6048042B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12442476A JPS6048042B2 (en) 1976-10-19 1976-10-19 Method for manufacturing a vibrating body for an acoustic transducer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12442476A JPS6048042B2 (en) 1976-10-19 1976-10-19 Method for manufacturing a vibrating body for an acoustic transducer

Publications (2)

Publication Number Publication Date
JPS5350703A JPS5350703A (en) 1978-05-09
JPS6048042B2 true JPS6048042B2 (en) 1985-10-25

Family

ID=14885129

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12442476A Expired JPS6048042B2 (en) 1976-10-19 1976-10-19 Method for manufacturing a vibrating body for an acoustic transducer

Country Status (1)

Country Link
JP (1) JPS6048042B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60185489A (en) * 1984-03-02 1985-09-20 Onkyo Corp Diaphragm for electroacoustic transducer
JPS60186197A (en) * 1984-03-05 1985-09-21 Onkyo Corp Diaphragm for electroacoustic transducer and its manufacturing method

Also Published As

Publication number Publication date
JPS5350703A (en) 1978-05-09

Similar Documents

Publication Publication Date Title
US3547676A (en) Pyrolytic carbon structures and process for making same
JPH1025576A (en) Sublimation method of raw material compound in cvd film formation method
JPS6048042B2 (en) Method for manufacturing a vibrating body for an acoustic transducer
Brennan et al. Heats of adsorption of oxygen on evaporated films of molybdenum, tungsten, cobalt and nickel at 77, 90 and 273° K, and nature of adsorbed layers
US2528454A (en) Coating process
US5294586A (en) Hydrogen-water vapor pretreatment of Fe-Cr-Al alloys
Roshan et al. The effect of the surface state on the hydrogen permeability and the catalytic activity of palladium alloy membranes
US4781734A (en) Non-porous hydrogen diffusion membrane and utilization thereof
US4196022A (en) Surface hardening method
JP2982055B2 (en) Method for producing fine metal particles of gold, silver or copper
JPS6229550B2 (en)
JPH01131002A (en) Production of hydrogen-occlusive alloy
JPS6123268B2 (en)
JP3342416B2 (en) Hydrogen purification membrane and hydrogen production method
US4866746A (en) Coated material and X-ray exposure mask
JPH01188401A (en) Production of thin film of hydrogen occluding alloy
JPS5815070A (en) Manufacture of thin plate
JPS589214A (en) Magnetic recording medium
JPS6350474A (en) Formation of magnetic thin film
Horton Anisotropic reaction kinetics of oxygen with pyrolytic graphite
JPS6047004A (en) Production of organic substance powder
JPS5857038B2 (en) Method for manufacturing diaphragm for electroacoustic transducer
JPS5822917B2 (en) speaker diaphragm
JP2627286B2 (en) Manufacturing method of hydrogen storage alloy
JPH02502549A (en) Vapor deposition method