JPH0240027B2 - HISANKABUTSUSERAMITSUKUSUYOSETSUCHAKUZAISHIITOOYOBI HISANKABUTSUSERAMITSUKUSUYOSETHICHAKUTSUUSERAMITSUKUSUNOSETSUCHAKUHOHO - Google Patents

HISANKABUTSUSERAMITSUKUSUYOSETSUCHAKUZAISHIITOOYOBI HISANKABUTSUSERAMITSUKUSUYOSETHICHAKUTSUUSERAMITSUKUSUNOSETSUCHAKUHOHO

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Publication number
JPH0240027B2
JPH0240027B2 JP14723485A JP14723485A JPH0240027B2 JP H0240027 B2 JPH0240027 B2 JP H0240027B2 JP 14723485 A JP14723485 A JP 14723485A JP 14723485 A JP14723485 A JP 14723485A JP H0240027 B2 JPH0240027 B2 JP H0240027B2
Authority
JP
Japan
Prior art keywords
adhesive
oxide
parts
silicon nitride
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
Application number
JP14723485A
Other languages
Japanese (ja)
Other versions
JPS627678A (en
Inventor
Nobuyuki Tamatoshi
Minoru Kinoshita
Yoshihiro Ehata
Makoto Pponda
Takashi Tominaga
Hideshi Asoshina
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.)
National Institute of Advanced Industrial Science and Technology AIST
Nitto Denko Corp
Original Assignee
Agency of Industrial Science and Technology
Nitto Denko 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 Agency of Industrial Science and Technology, Nitto Denko Corp filed Critical Agency of Industrial Science and Technology
Priority to JP14723485A priority Critical patent/JPH0240027B2/en
Publication of JPS627678A publication Critical patent/JPS627678A/en
Publication of JPH0240027B2 publication Critical patent/JPH0240027B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Adhesives Or Adhesive Processes (AREA)
  • Ceramic Products (AREA)

Description

【発明の詳现な説明】 産業䞊の利甚分野 本発明は、シヌト状の非酞化物セラミツクス甚
接着剀及び非酞化物セラミツクスの接着方法に関
する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to an adhesive for sheet-shaped non-oxide ceramics and a method for bonding non-oxide ceramics.

埓来技術ずその問題点 窒化ケむ玠や炭化ケむ玠などの非酞化物セラミ
ツクスは、金属に比べお高枩匷床、耐食性、耐摩
耗性等に優れおいるので、高枩甚郚材ずしお脚光
を济びおおり、ガスタヌビン、自動車゚ンゞン、
熱亀換噚等ぞの応甚開発が進められおいる。
Conventional technology and its problems Non-oxide ceramics such as silicon nitride and silicon carbide have superior high-temperature strength, corrosion resistance, and wear resistance compared to metals, so they are attracting attention as high-temperature components, and are used in gas turbines. , car engine,
Application development for heat exchangers, etc. is underway.

䞊蚘の劂き各皮甚途においお、非酞化物セラミ
ツクスにその優れた機胜を十分に発揮させるため
には、補造工皋で、これ等非酞化物セラミツクス
盞互を接着させるこずが必芁ずな぀おくる。特に
非酞化物セラミツクス成圢䜓は、耇雑な圢状に成
圢及び加工するこずが困難なので、単玔な圢状の
郚材から耇雑な圢状に組み立おる必芁があり、非
酞化物セラミツクス郚材盞互の接着技術の開発が
䞍可欠である。
In order for non-oxide ceramics to fully exhibit their excellent functions in the various uses mentioned above, it is necessary to bond these non-oxide ceramics together during the manufacturing process. In particular, it is difficult to mold and process non-oxide ceramic molded bodies into complex shapes, so it is necessary to assemble simple-shaped members into complex shapes, and it is essential to develop adhesive technology for mutually bonding non-oxide ceramic parts. It is.

しかしながら、非酞化物セラミツクスは、䞀般
に溶融物に察する芪和性、いわゆる濡れ性が極め
お悪く、しかもアルミナ、マグネシア等の酞化物
系セラミツクスずは異なり、共有結合性が匷く、
たた各皮物質に察する反応性も非垞に䜎いため
に、その接着は極めお困難である。
However, non-oxide ceramics generally have extremely poor affinity for molten materials, so-called wettability, and unlike oxide ceramics such as alumina and magnesia, they have strong covalent bonds.
Furthermore, since the reactivity to various substances is extremely low, adhesion is extremely difficult.

埓来、非酞化物セラミツクスの接着には、接着
剀を被接着郚材間に介圚させるか、あるいは䜕も
介圚させるこずなく、高枩高圧䞋でホツトプレス
する方法がずられおいた。しかしながら、ホツト
プレス法では、高枩及び高圧を必芁ずするので、
耇雑なあるいは倧型の郚材の接着は極めお困難で
ある。たた、最近脚光を济びおいる熱間等方加圧
法いわゆるHIP法にも、同様な問題点が存圚す
る。
Conventionally, non-oxide ceramics have been bonded by interposing an adhesive between the members to be bonded, or by hot pressing at high temperature and pressure without intervening any adhesive. However, the hot press method requires high temperature and pressure, so
Bonding complex or large components is extremely difficult. Similar problems also exist in the hot isostatic pressing method, so-called HIP method, which has recently been in the spotlight.

したが぀お、倧型で耇雑な圢状の郚材を組立お
るには、圧力を芁せず、加熱するだけで容易に接
着できる接着剀の開発が望たれおいる。埓来、非
酞化物セラミツクス甚接着剀ずしおは、−族
酞化物単独、アルミナ−シリカ−アルカリ土類金
属酞化物系、フツ化カルシりム−カオリン系、あ
るいはこれに垌土類酞化物を少量添加したもの等
が䜿甚されおいる。しかしながら、これらは、各
れも酞化物系ガラスによる接着剀であり、非酞化
物セラミツクスずの熱膚脹係数の違いなどによ
り、䞀般に接着匷床が䜎く、非酞化物セラミツク
ス成圢䜓の優れた特性を十分に生かすにはいた぀
おいない。
Therefore, in order to assemble large, complex-shaped members, it is desired to develop an adhesive that can be easily bonded by simply heating without requiring pressure. Conventionally, adhesives for non-oxide ceramics include -A group oxide alone, alumina-silica-alkaline earth metal oxide system, calcium fluoride-kaolin system, or adhesives with a small amount of rare earth oxide added thereto. is used. However, these are all adhesives based on oxide glass, and due to differences in coefficient of thermal expansion with non-oxide ceramics, their adhesive strength is generally low, and the excellent properties of non-oxide ceramic molded products cannot be fully demonstrated. I haven't gotten to the point where I can take advantage of it.

本発明者等は、この様な珟状に鑑みお、皮々研
究を重ねた結果、窒化ケむ玠、酞化マグネシりム
及び皮以䞊の垌土類酞化物を有効成分ずする非
酞化物セラミツクス甚接着剀を完成した特願昭
59−82712号。この接着剀は、垂販されおいる非
酞化物セラミツクスの垞圧焌結品の匷床䟋え
ば、窒化ケむ玠で玄53Kgmm2、炭化ケむ玠で玄50
Kgmm2に近い接着匷床を瀺し、しかも匷床を玄
900℃たで維持するずいう優れた性胜を有しおい
る。しかしながら、この接着剀は、粉末状、ペレ
ツト状又はペヌスト状であるので、これを湟曲面
や凹凞郚分等の耇雑な圢状の郚材の接合に甚いる
堎合には、䜜業時に所定の接着郚䜍に所望の厚さ
に䞔぀均䞀に付䞎するこずは、極めお困難であ
る。埓぀お、䜜業性の改善及び接着特性のばら぀
き防止の芳点から改善の䜙地が残されおいる。
In view of the current situation, the present inventors have conducted various studies and have completed an adhesive for non-oxide ceramics containing silicon nitride, magnesium oxide, and two or more rare earth oxides as active ingredients ( special request
59-82712). This adhesive has the strength of pressureless sintered products of commercially available non-oxide ceramics (for example, about 53 Kg/mm 2 for silicon nitride and about 50 Kg/mm 2 for silicon carbide).
Kg/mm 2 ), and the strength is approximately
It has excellent performance of maintaining up to 900℃. However, since this adhesive is in the form of powder, pellets, or paste, when it is used to join members with complex shapes such as curved surfaces or uneven parts, it is necessary to apply the adhesive to the desired bonding area during work. It is extremely difficult to apply it thickly and uniformly. Therefore, there is still room for improvement in terms of improving workability and preventing variations in adhesive properties.

問題点を解決するための手段 本発明者は、特願昭59−82712号に瀺された非
酞化物セラミツクス甚接着剀の優れた特性を曎に
䞀局改善すべく匕続き研究を重ねた結果、接着剀
にバむンダヌ成分を加え、これをシヌト状に成圢
する堎合には、接合すべき郚材の圢状の劂䜕にか
かわらず、任意の接着郚䜍に所望の厚さの接着剀
を均䞀に䞔぀容易に付䞎するこずが出来、その結
果、接着特性のばら぀きも抑制されるこずを芋出
した。即ち、本発明は、窒化ケむ玠、酞化マグネ
シりム及び皮以䞊の垌土類酞化物を有効成分ず
する接着剀成分ずバむンダヌずを均䞀に混合、成
圢しおなる非酞化物セラミツクス甚接着剀シヌト
を提䟛する。
Means for Solving the Problems As a result of continued research to further improve the excellent properties of the adhesive for non-oxide ceramics disclosed in Japanese Patent Application No. 59-82712, the inventor discovered that the adhesive When adding a binder component to and forming this into a sheet, the desired thickness of adhesive can be applied uniformly and easily to any bonding site, regardless of the shape of the members to be bonded. It has been found that as a result, variations in adhesive properties are suppressed. That is, the present invention provides an adhesive sheet for non-oxide ceramics, which is formed by uniformly mixing and molding an adhesive component containing silicon nitride, magnesium oxide, and two or more rare earth oxides as active ingredients and a binder. .

本発明は、曎に、窒化ケむ玠、酞化マグネシり
ム及び皮以䞊の垌土類酞化物を有効成分ずする
接着剀成分ずバむンダヌずを均䞀に混合、成圢し
おなるシヌトを非酞化物セラミツクス盞互間に介
圚させ、非酞化性雰囲気䞋1400〜1800℃の枩床で
加熱するこずを特城ずする非酞化物セラミツクス
の接着方法をも提䟛する。
The present invention further provides a sheet formed by uniformly mixing and molding an adhesive component containing silicon nitride, magnesium oxide, and two or more rare earth oxides and a binder as active ingredients, and interposing the sheet between the non-oxide ceramics. The present invention also provides a method for bonding non-oxide ceramics, characterized by heating at a temperature of 1400 to 1800° C. in a non-oxidizing atmosphere.

本発明の接着剀が適甚される非酞化物セラミツ
クスは、材質的には、䟋えば、窒化ケむ玠、炭化
ケむ玠、サむアロン、窒化アルミニりム等であ
り、ホツトプレス、垞圧焌結、あるいは反応焌結
等のいずれの方法で埗られるものであ぀おもよ
く、特にその圢状や倧きさに限定はなく、しかも
接着すべき郚材は同䞀圢状でも異圢状でもよい。
Non-oxide ceramics to which the adhesive of the present invention is applied include, for example, silicon nitride, silicon carbide, sialon, aluminum nitride, etc., and can be made by hot pressing, pressureless sintering, reaction sintering, etc. There are no particular limitations on the shape or size, and the members to be bonded may have the same shape or different shapes.

本発明接着剀シヌトにおいお有効成分である窒
化ケむ玠ずしおは、垂販のものをいずれも䜿甚で
き、特にその補法、粒床、玔床等は限定されな
い。たた、粉末状態のものだけでなく、りむスカ
ヌ状態のものも甚いるこずができる。接着匷床を
高めるためには、玔床の高いものの方が望たし
い。
As silicon nitride, which is an active ingredient in the adhesive sheet of the present invention, any commercially available silicon nitride can be used, and its manufacturing method, particle size, purity, etc. are not particularly limited. Furthermore, not only those in powder form but also those in whisker form can be used. In order to increase adhesive strength, it is desirable to use a material with high purity.

たた、酞化マグネシりムずしおは、通垞垂販さ
れおいるものをいずれも䜿甚でき、その玔床及び
粒床は、特に限定されないが、接着匷床を高める
ためには、できるだけ高玔床で粒床の小さいもの
が望たしい。
Further, as magnesium oxide, any commercially available magnesium oxide can be used, and its purity and particle size are not particularly limited, but in order to increase adhesive strength, it is desirable to have as high a purity as possible and a particle size as small as possible.

たた、本発明の接着剀シヌトのもう䞀぀の有効
成分である垌土類酞化物ずしおは、皮以䞊の垌
土類酞化物を甚いるこずが必芁である。垌土類酞
化物を皮だけ甚いる堎合には、非酞化物セラミ
ツクスに察する十分な濡れ性が埗られないため
に、満足のいく接着匷床を埗るこずができない。
垌土類酞化物の組み合せずしおは、特に限定され
ないが、酞化むツトリりムず酞化ランタンの組み
合せが最適である。䜿甚する垌土類酞化物の玔床
及び粒床は特に限定されないが、接着匷床を高め
るには、できるだけ高玔床で、粒床の小さいもの
が望たしい。
Further, as the rare earth oxide which is another active ingredient of the adhesive sheet of the present invention, it is necessary to use two or more kinds of rare earth oxides. If only one type of rare earth oxide is used, sufficient adhesive strength cannot be obtained because sufficient wettability with respect to non-oxide ceramics cannot be obtained.
The combination of rare earth oxides is not particularly limited, but a combination of yttrium oxide and lanthanum oxide is optimal. The purity and particle size of the rare earth oxide used are not particularly limited, but in order to increase adhesive strength, it is desirable to have as high a purity as possible and a small particle size.

本発明の接着剀の有効成分のうち、窒化ケむ玠
ず垌土類酞化物ずの配合割合は、窒化ケむ玠ず垌
土類酞化物の合蚈を100molずした堎合に、窒
化ケむ玠を35〜65molずし、垌土類酞化物のう
ちの皮を酞化むツトリりムずしお、これの含有
量を10〜35molずし、残郚を少なくずも皮の
他の垌土類酞化物ずするこずが奜たしい。特に、
窒化ケむ玠を40〜55mol、酞化むツトリりムを
15〜30mol、残郚を他の垌土類酞化物の少なく
ずも皮ずした堎合に、非垞に匷い接着匷床が埗
られる。
Among the active ingredients of the adhesive of the present invention, the blending ratio of silicon nitride and rare earth oxide is 35 to 65 mol% of silicon nitride and 35 to 65 mol% of silicon nitride and rare earth oxide. It is preferable that one of the oxides is yttrium oxide, the content of which is 10 to 35 mol %, and the remainder is at least one other rare earth oxide. especially,
40-55 mol% silicon nitride, yttrium oxide
Very strong adhesive strength can be obtained when the amount is 15 to 30 mol % and the remainder is at least one other rare earth oxide.

たた、酞化マグネシりムの添加量は、䞊蚘の窒
化ケむ玠ず垌土類酞化物の混合物に察しお倖掛け
で10〜80wt添加するのが最適である。10wt
未満及び80wtを超える堎合には該接着剀の非
酞化物セラミツクスに察する濡れが十分でなく、
満足すべき接着䜜甚は埗られない。
Further, the optimum amount of magnesium oxide to be added is 10 to 80 wt%, based on the above-mentioned mixture of silicon nitride and rare earth oxide. 10wt%
If it is less than 80wt% or more than 80wt%, the adhesive will not wet the non-oxide ceramics sufficiently;
A satisfactory adhesive effect cannot be obtained.

本発明においお有効な組成範囲を䞊蚘範囲ずし
た理由は、この範囲内であれば接着剀の有効成分
が溶融しお、良奜な濡れが埗られるずずもに、窒
化ケむ玠を適量含むので、該接着剀の熱膚脹係数
が被接着䜓の非酞化物セラミツクス成圢䜓の熱膚
脹係数に近くなり、接着埌の接着剀局内の残留ひ
ずみがほずんどないためである。
The reason why the effective composition range in the present invention is set to the above range is that within this range, the active ingredients of the adhesive will melt and good wetting will be obtained, and since it will contain an appropriate amount of silicon nitride, the adhesive will This is because the coefficient of thermal expansion is close to that of the non-oxide ceramic molded body to be adhered, and there is almost no residual strain in the adhesive layer after bonding.

本発明においお、窒化ケむ玠、酞化マグネシり
ム及び皮以䞊の垌土類酞化物を有効成分ずする
接着剀成分をシヌト状に成圢するために䜿甚する
バむンダヌずしおは、接着操䜜枩床にいたる昇枩
過皋でのガス発生量が少なく、䞔぀分解埌に接着
を阻害する残枣を生じない゚ラストマヌが奜適で
ある。この様な゚ラストマヌずしおは、゚チレン
−プロピレン共重合䜓、゚チレン−プロピレン−
ゞ゚ンタ−ポリマヌ、ポリむ゜ブチレン、ポリむ
゜プレン、スチレン−ブタゞ゚ン共重合䜓などの
合成ゎム類、倩然ゎム類或いぱチレン−酢酞ビ
ニル共重合䜓などの合成暹脂等が䟋瀺され、これ
等の皮又は皮以䞊を䜿甚する。バむンダヌの
分子量は特に限定されないが、良奜なシヌト成圢
性を保持する為には、平均分子量䞇〜100侇繋
床ずするこずが奜たしい。これ等の゚ラストマヌ
には、必芁に応じ、接着性改善の目的でアルキル
プノヌル系、クマロン−むンデン系、ポリテル
ペン系、ロゞン系、石油系、ポリビニル゚ヌテル
系等の暹脂の皮又は皮以䞊を䜵甚しおも良
く、曎に軟化剀ずしおキシレン系暹脂、パラフむ
ンワツクス、プロセスオむル、アビ゚チルアルコ
ヌル等を配合しおも良い。
In the present invention, the binder used to form the adhesive component containing silicon nitride, magnesium oxide, and two or more rare earth oxides as active ingredients into a sheet shape is An elastomer that generates a small amount and does not produce a residue that inhibits adhesion after decomposition is suitable. Such elastomers include ethylene-propylene copolymer, ethylene-propylene copolymer,
Examples include synthetic rubbers such as dienterpolymer, polyisobutylene, polyisoprene, styrene-butadiene copolymer, natural rubbers, and synthetic resins such as ethylene-vinyl acetate copolymer, and one or two of these. Use the above. The molecular weight of the binder is not particularly limited, but in order to maintain good sheet formability, the average molecular weight is preferably about 50,000 to 1,000,000. If necessary, these elastomers may be combined with one or more of alkylphenol-based, coumaron-indene-based, polyterpene-based, rosin-based, petroleum-based, and polyvinyl ether-based resins for the purpose of improving adhesion. Furthermore, a xylene resin, paraffin wax, process oil, abiethyl alcohol, etc. may be added as a softening agent.

尚、䞊蚘゚ラストマヌ或いぱラストマヌず他
の䜵甚成分からなるバむンダヌは、耇雑な圢状の
郚材接着時に接着剀シヌトが折り曲げ或いは湟曲
によりクラツクを生じない様に、25℃で0.1〜50
Kgmm2皋床、より奜たしくは0.5〜40Kgmm2皋床
の匟性率を有するものを遞択するこずが望たし
い。ここに、匟性率ずは、枩床25℃においお詊料
をチダツク間距離50mmで300mmminの速床で匕
き䌞ばした堎合の䞋匏で瀺される接線モゞナラス
を意味するものずする。
In addition, the binder made of the above elastomer or the elastomer and other combined components should be used at a temperature of 0.1 to 50% at 25°C to prevent the adhesive sheet from cracking due to bending or curving when bonding parts with complex shapes.
It is desirable to select one having an elastic modulus of about Kg/mm 2 , more preferably about 0.5 to 40 Kg/mm 2 . Here, the elastic modulus refers to the tangential modulus expressed by the following formula when a sample is stretched at a speed of 300 mm/min with a chuck distance of 50 mm at a temperature of 25°C.

匟性率 䜆し、 詊料を100䌞ばした点ず接線ずの亀点の力
Kgmm2 詊料の断面積mm2 接着剀成分に察するバむンダヌの配合割合は、
加熱接着時のガス発生や分解残枣による接着特性
ぞの圱響を出来るだけ少なくし぀぀も同時に良奜
なシヌト成圢性及び柔軟な接着剀シヌト匟性率
0.3〜45Kgmm2、曲率半埄10mm以䞋を埗るため
に、前者100重量郚に察し埌者〜50重量郚皋床、
より奜たしくは〜25重量郚皋床ずするこずが望
たしい。曎に、バむンダヌの配合割合は、接着剀
成分の粒埄りむスカヌを䜿甚する堎合には、そ
の埄及び長さをも考慮しお定めるこずが奜たし
い。䞀般に、接着剀成分の粒埄が倧きくなれば、
バむンダヌの配合量を枛少するこずが可胜ずなる
が、その反面接着剀の濡れ性が䜎䞋する。埓぀
お、接着特性及び成圢性に優れた接着剀シヌトを
埗る為には、接着剀成分の平均粒埄〜10Ό皋
床のずき、接着剀成分100重量郚に察するバむン
ダヌ配合量を10〜20重量郚ずするのが最適であ
る。
Elastic modulus = F/S However, F: Force at the intersection of the point where the sample is stretched 100% and the tangent line (Kg/mm 2 ) S: Cross-sectional area of the sample (mm 2 ) The blending ratio of the binder to the adhesive component is:
While minimizing the effects of gas generation and decomposition residue on adhesive properties during heat bonding, it also provides good sheet formability and a flexible adhesive sheet (elastic modulus).
0.3 to 45 Kg/mm 2 and radius of curvature of 10 mm or less), the latter is approximately 3 to 50 parts by weight per 100 parts by weight of the former.
More preferably, the amount is about 5 to 25 parts by weight. Furthermore, it is preferable that the blending ratio of the binder is determined in consideration of the particle size of the adhesive component (if whiskers are used, their diameter and length). Generally, the larger the particle size of the adhesive component, the more
Although it becomes possible to reduce the amount of binder blended, the wettability of the adhesive on the other side decreases. Therefore, in order to obtain an adhesive sheet with excellent adhesive properties and moldability, when the average particle size of the adhesive component is about 1 to 10 ÎŒm, the amount of binder blended is 10 to 20 parts by weight per 100 parts by weight of the adhesive component. It is best to

本発明接着剀シヌトは、皮々の方法により補造
可胜である。䟋えば、バむンダヌをアセトン、ト
ル゚ン、メチル゚チルケトン等の有機溶剀に溶解
した埌、接着剀成分を加え、均䞀に混緎する。次
いで、混緎物を離型玙を被せた型枠䞊に流し蟌
み、溶剀を蒞発させた埌、成圢物を圧延ロヌルに
通しおシヌト状又はフむルム状、或いはその他の
圢状に成圢する。成圢は、抌し出し、プレス圧
延、ドクタヌブレヌト法等の他の任意の方法によ
぀おも行ない埗るこずは、蚀うたでもない。
The adhesive sheet of the present invention can be manufactured by various methods. For example, after dissolving the binder in an organic solvent such as acetone, toluene, or methyl ethyl ketone, an adhesive component is added and kneaded uniformly. Next, the kneaded product is poured onto a mold covered with release paper, and after the solvent is evaporated, the molded product is passed through rolling rolls and formed into a sheet, film, or other shape. It goes without saying that the shaping can also be carried out by any other method such as extrusion, press rolling, and doctor blasting.

本発明の接着剀シヌトを䜿甚しお非酞化物セラ
ミツクスの接着を行なうには、非酞化物セラミツ
クス郚材の被接着面間に所定圢状に切断若しくは
加工した接着剀シヌトを介圚させた状態で、郚材
の加熱を行なう。接着剀シヌトの厚さは、接着剀
成分の組成、加熱条件、郚材の圢状等に応じお適
宜決定されるが、通垞接着剀成分の付䞎量が、接
着面積cm2圓り0.01〜皋床、より奜たしくは
0.05〜0.3皋床ずなる様にすれば良い。
In order to bond non-oxide ceramics using the adhesive sheet of the present invention, the adhesive sheet cut or processed into a predetermined shape is interposed between the surfaces of the non-oxide ceramic members to be bonded. Heating is performed. The thickness of the adhesive sheet is determined appropriately depending on the composition of the adhesive component, heating conditions, shape of the member, etc., but usually the amount of adhesive component applied is about 0.01 to 1 g per 1 cm 2 of adhesive area, or more. Preferably
The amount may be adjusted to about 0.05 to 0.3 g.

本発明の接着方法においお、接着剀シヌトを非
酞化物セラミツクス成圢䜓郚材間に介圚させお加
熱凊理する枩床は、1400〜1800℃の範囲ずする。
加熱枩床が、1400℃未満では、接着剀成分が溶融
しないため接着䜜甚が発揮されず、䞀方、1800℃
を超える堎合には、被接着䜓である非酞化物セラ
ミツクス成圢䜓郚材の倉圢或いは倉質が生じた
り、たた接着剀有効成分の蒞発も進み、曎に、熱
効率の面からも奜たしくない。
In the bonding method of the present invention, the temperature at which the adhesive sheet is heat-treated with the adhesive sheet interposed between the non-oxide ceramic molded members is in the range of 1400 to 1800°C.
If the heating temperature is less than 1400℃, the adhesive component will not melt and the adhesive effect will not be exhibited;
If it exceeds the above range, the non-oxide ceramic molded member to be adhered may be deformed or deteriorated, and the active ingredients of the adhesive may also evaporate, which is also undesirable from the standpoint of thermal efficiency.

熱凊理雰囲気ずしおは、真空、䞍掻性ガス、窒
玠ガス等の非酞化性雰囲気が䜿甚され、なかでも
真空䞭あるいは窒玠雰囲気䞋で加熱凊理するこず
が望たしい。
As the heat treatment atmosphere, a non-oxidizing atmosphere such as a vacuum, an inert gas, or a nitrogen gas is used, and it is particularly preferable to perform the heat treatment in a vacuum or a nitrogen atmosphere.

䜜 甹 本発明の接着剀シヌトを甚いるこずにより、卓
越した接着効果が発揮される理由は、珟圚なお明
確ではないが、以䞋の劂く掚定される。
Function The reason why the adhesive sheet of the present invention exhibits an excellent adhesive effect is not yet clear, but it is presumed as follows.

即ち、本発明の接着剀シヌトの接着剀成分は、
および1400〜1800℃の融点を有するので、接着剀
シヌトを介圚させた非酞化物セラミツクス成圢䜓
郚材を1400℃以䞊に加熱するず、接着剀成分が溶
融しお非酞化物セラミツクス成圢䜓郚材衚面を十
分に濡らすこずができ、たた非酞化物セラミツク
ス成圢䜓郚ずの間で䜕らかの反応が起こり、非酞
化物セラミツクス成圢䜓郚材盞互を匷固に接着す
るものず考えられる。接着剀有効成分が、酞化マ
グネシりムず皮以䞊の垌土類酞化物ずの組み合
せの堎合には、同様な機構により、䞀応接着は可
胜ではあるが、充分な匷床は埗られない。このこ
ずから、接着剀有効成分ずしお窒化ケむ玠を含む
こずにより、接着剀の熱膚脹係数が非酞化物セラ
ミツクス成圢䜓郚材の熱膚脹係数に近くなり、そ
の結果、接着埌の接着局内の残留ひずみが小さ
く、高い接着匷床が埗られるものず考えられる。
That is, the adhesive component of the adhesive sheet of the present invention is:
and has a melting point of 1,400 to 1,800°C, so when a non-oxide ceramic molded member with an adhesive sheet interposed is heated to 1,400°C or higher, the adhesive component melts and the surface of the non-oxide ceramic molded member is sufficiently heated. It is thought that some kind of reaction occurs between the non-oxide ceramic molded body parts and the non-oxide ceramic molded body parts are firmly bonded to each other. When the adhesive active ingredient is a combination of magnesium oxide and two or more rare earth oxides, adhesion is possible to some extent by a similar mechanism, but sufficient strength cannot be obtained. From this, by including silicon nitride as an adhesive active ingredient, the coefficient of thermal expansion of the adhesive becomes close to that of the non-oxide ceramic molded member, and as a result, the residual strain in the adhesive layer after bonding is reduced. It is thought that high adhesive strength can be obtained.

発明の効果 本発明によれば、埓来方法では接着困難であ぀
た倧型、耇雑、異圢の非酞化物セラミツクス郚材
盞互を容易に、しかも匷力に接着できる。たた、
接着埌圢成される接着局が化孊的に安定であり、
900℃たで充分な耐熱性を有する。曎に、本発明
の接着剀シヌトは、0.05〜mm適床たで均䞀な厚
さで圧延可胜なので、加熱凊理に圢成される接着
厚さも䞀定ずなり、接着特性のばら぀きも少な
い。曎にたた、本発明の接着剀シヌトは、切断及
び倉圢が可胜なので、圢状耇雑な郚材の接合も可
胜ずなり、䜜業性を倧巟に改善する。埓぀お、非
酞化物セラミツクスは、その優れた機胜を曎に䞀
局発揮できる。
Effects of the Invention According to the present invention, large, complex, and irregularly shaped non-oxide ceramic members, which have been difficult to bond using conventional methods, can be easily and strongly bonded to each other. Also,
The adhesive layer formed after adhesion is chemically stable,
Has sufficient heat resistance up to 900℃. Furthermore, since the adhesive sheet of the present invention can be rolled to a uniform thickness of approximately 0.05 to 5 mm, the adhesive thickness formed by heat treatment is also constant, and there is little variation in adhesive properties. Furthermore, since the adhesive sheet of the present invention can be cut and deformed, it is also possible to join members with complicated shapes, greatly improving workability. Therefore, non-oxide ceramics can exhibit its excellent functions even further.

実斜䟋 以䞋、実斜䟋にもずづき本発明を曎に詳现に説
明する。
EXAMPLES Hereinafter, the present invention will be explained in more detail based on examples.

実斜䟋  窒化ケむ玠りむスカヌ埄0.5〜2Ό、長さ50
〜300Ό45mol、酞化むツトリりム27.5mol
及び酞化ランタン27.5molからなる混合粉末
100重量郚に酞化マグネシりム30重量郚を添加混
合し、接着剀成分ずした。次いで該接着剀成分
100重量郚に察し、バむンダヌずしおブチルゎム
分子量玄25䞇20重量郚及び溶剀ずしおトル゚
ン30重量郚を加えお混合した埌、玄50℃に加熱し
たロヌルにおトル゚ンを気化させながら充分に混
緎し、垞枩でロヌル圧延し、厚さ100Όの本発
明の接着剀シヌトを埗た。埗られた接着剀シヌト
は、匟性率3.6Kgmm2、曲率半埄0.5mm以䞋であ぀
た。
Example 1 Silicon nitride whiskers (diameter 0.5 to 2 ÎŒm, length 50
~300ÎŒm) 45mol%, yttrium oxide 27.5mol
% and lanthanum oxide 27.5mol%
30 parts by weight of magnesium oxide was added to 100 parts by weight to form an adhesive component. Then the adhesive component
To 100 parts by weight, 20 parts by weight of butyl rubber (molecular weight approximately 250,000) as a binder and 30 parts by weight of toluene as a solvent were added and mixed, and then thoroughly kneaded with rolls heated to approximately 50°C while vaporizing the toluene. , and rolled at room temperature to obtain an adhesive sheet of the present invention having a thickness of 100 Όm. The obtained adhesive sheet had an elastic modulus of 3.6 Kg/mm 2 and a radius of curvature of 0.5 mm or less.

この接着剀シヌトを10×10mm2に切断し、10×10
×15mm3の個の窒化ケむ玠成圢䜓間にはさみ蟌
み、窒玠雰囲気䞭、1600℃で時間加熱凊理し
た。
Cut this adhesive sheet into 10 x 10 mm 2 and 10 x 10
It was sandwiched between two silicon nitride molded bodies measuring 15 mm 3 and heat-treated at 1600° C. for 1 hour in a nitrogen atmosphere.

埗られた接着䜓詊料から××30mm3の角棒
を切り出し、スパン20mm、荷重速床0.5mmmin
の条件䞋に䞉点曲げ詊隓を行な぀た結果、32.5
Kgmm2の匷床が埗られた。
A square bar of 3 x 3 x 30 mm was cut out from the obtained adhesive sample, with a span of 20 mm and a loading rate of 0.5 mm/min.
As a result of a three-point bending test under the conditions of 32.5
A strength of Kg/mm 2 was obtained.

実斜䟋  窒化ケむ玠粉末平均粒埄15Ό45mol、
酞化むツトリりム27.5mol及び酞化ランタン
27.5molからなる混合粉末100重量郚に酞化マ
グネシりム30重量郚を添加混合し、接着剀成分ず
した。
Example 2 Silicon nitride powder (average particle size 15 ÎŒm) 45 mol%,
Yttrium oxide 27.5mol% and lanthanum oxide
30 parts by weight of magnesium oxide was added to 100 parts by weight of a mixed powder consisting of 27.5 mol % to form an adhesive component.

該接着剀成分100重量郚にバむンダヌずしおア
クリルゎム25重量郚及び溶剀ずしおトル゚ン30重
量郚を加え、実斜䟋ず同様の方法により、厚さ
300Ό、匟性率2.4Kgmm2、曲率半埄0.5mm以䞋の
本発明の接着剀シヌトを埗た。
25 parts by weight of acrylic rubber as a binder and 30 parts by weight of toluene as a solvent were added to 100 parts by weight of the adhesive component, and the thickness was determined by the same method as in Example 1.
An adhesive sheet of the present invention having a diameter of 300 ÎŒm, an elastic modulus of 2.4 Kg/mm 2 and a radius of curvature of 0.5 mm or less was obtained.

この接着剀シヌトを所定の倧きさに切断し、窒
化ケむ玠成圢䜓間にはさみ蟌み、窒玠雰囲気䞭、
1650℃で時間加熱凊理した。
This adhesive sheet was cut to a predetermined size, sandwiched between silicon nitride molded bodies, and placed in a nitrogen atmosphere.
Heat treatment was performed at 1650°C for 1 hour.

埗られた接着䜓詊料の䞉点曲げ匷床は32.4Kg
mm2であ぀た。
The three-point bending strength of the obtained adhesive sample was 32.4 kg/
It was warm in mm2 .

実斜䟋  窒化ケむ玠粉末平均粒埄15Ό55mol、
酞化むツトリム22.5mol及び酞化ランタン
22.5molからなる混合粉末100重量郚に、酞化
マグネシりム20重量郚を添加し、総平均粒埄玄
〜7Όの接着剀有効成分ずした。
Example 3 Silicon nitride powder (average particle size 15 ÎŒm) 55 mol%,
Ittrim oxide 22.5mol% and lanthanum oxide
20 parts by weight of magnesium oxide was added to 100 parts by weight of mixed powder consisting of 22.5 mol%, and the total average particle size was about 3.
~7ÎŒm adhesive active ingredient.

䞊蚘有効成分100重量郚にバむンダヌずしおブ
タゞ゚ンゎム15重量郚及び溶剀ずしおトル゚ン30
重量郚を加え、充分に混緎した埌、50℃で180分
間也燥し、垞枩でロヌル圧延し、厚さ玄mmのシ
ヌトずし、曎に埗られたシヌトをプレスにかけお
厚さ300Όの本発明の接着剀シヌトを埗た。
100 parts by weight of the above active ingredient, 15 parts by weight of butadiene rubber as a binder and 30 parts by weight of toluene as a solvent.
After adding parts by weight and thoroughly kneading, the adhesive of the present invention was dried at 50°C for 180 minutes, rolled at room temperature to form a sheet with a thickness of about 1 mm, and the obtained sheet was further pressed to have a thickness of 300 Όm. Got a sheet.

䞊蚘接着剀シヌトは、匟性率1.4Kgmm2、曲率
半埄0.5mm以䞋の倀を瀺した。
The adhesive sheet had an elastic modulus of 1.4 Kg/mm 2 and a radius of curvature of 0.5 mm or less.

この接着剀シヌトを、10×10mm2に切断し、10×
10×15mm3の炭化ケむ玠成圢䜓間にはさみ蟌み、
アルゎン雰囲気䞭1700℃で30分間加熱凊理した。
Cut this adhesive sheet into 10 x 10 mm 2 pieces,
Sandwiched between 10 x 15 mm 3 silicon carbide molded bodies,
Heat treatment was performed at 1700°C for 30 minutes in an argon atmosphere.

埗られた接着䜓詊料から、××30mm3の角
棒を切り出し、スパン20mm、荷重速床0.5mm
minの条件䞋で䞉点曲げ詊隓を行な぀たずころ、
28.5Kgmm2の匷床が埗られた。
A square bar of 3 x 3 x 30 mm was cut out from the obtained adhesive sample, and the span was 20 mm and the loading speed was 0.5 mm/
When a three-point bending test was conducted under conditions of min.
A strength of 28.5Kg/mm 2 was obtained.

実斜䟋  窒化ケむ玠りむスカヌ埄0.5〜20Ό、長さ50
〜300Ό55mol、酞化むツトリりム22.5mol
及び酞化ランタン22.5molの混合粉末100重
量郚に、酞化マグネシりム30重量郚を添加し、接
着剀有効成分ずした。
Example 4 Silicon nitride whiskers (diameter 0.5 to 20 ÎŒm, length 50
~300ÎŒm) 55mol%, yttrium oxide 22.5mol
30 parts by weight of magnesium oxide was added to 100 parts by weight of a mixed powder of 22.5 mol% of lanthanum oxide and 22.5 mol% of lanthanum oxide to form an adhesive active ingredient.

䞊蚘有効成分100重量郚に察し、バむンダヌず
しおブチルゎム重量郚及び溶剀ずしおトル゚ン
30重量郚を加え、充分混緎した埌、ドクタヌブレ
ヌド法により厚さ玄50Ό、曲率半埄0.5mm以䞋の
本発明のフむルム状接着剀組成物を埗た。
For 100 parts by weight of the above active ingredient, 5 parts by weight of butyl rubber as a binder and toluene as a solvent.
After adding 30 parts by weight and thoroughly kneading, a film-like adhesive composition of the present invention having a thickness of about 50 ÎŒm and a radius of curvature of 0.5 mm or less was obtained by a doctor blade method.

このフむルム状接着剀も、優れた接着特性を瀺
した。
This film adhesive also showed excellent adhesive properties.

Claims (1)

【特蚱請求の範囲】  窒化ケむ玠、酞化マグネシりム及び皮以䞊
の垌土類酞化物を有効成分ずする接着剀成分ずバ
むンダヌずを均䞀に混合、成圢しおなる非酞化物
セラミツクス甚接着剀シヌト。  窒化ケむ玠、酞化マグネシりム及び皮以䞊
の垌土類酞化物を有効成分ずする接着剀成分ずバ
むンダヌずを均䞀に混合、成圢しおなるシヌトを
非酞化物セラミツクス盞互間に介圚させ、非酞化
性雰囲気䞋1400〜1800℃の枩床で加熱するこずを
特城ずする非酞化物セラミツクスの接着方法。
[Scope of Claims] 1. An adhesive sheet for non-oxide ceramics formed by uniformly mixing and molding an adhesive component containing silicon nitride, magnesium oxide, and two or more rare earth oxides as active ingredients and a binder. 2. A sheet formed by uniformly mixing and molding an adhesive component containing silicon nitride, magnesium oxide, and two or more rare earth oxides and a binder as active ingredients is interposed between non-oxide ceramics and placed in a non-oxidizing atmosphere. A method for bonding non-oxide ceramics characterized by heating at a temperature of 1400 to 1800℃.
JP14723485A 1985-07-04 1985-07-04 HISANKABUTSUSERAMITSUKUSUYOSETSUCHAKUZAISHIITOOYOBI HISANKABUTSUSERAMITSUKUSUYOSETHICHAKUTSUUSERAMITSUKUSUNOSETSUCHAKUHOHO Expired - Lifetime JPH0240027B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14723485A JPH0240027B2 (en) 1985-07-04 1985-07-04 HISANKABUTSUSERAMITSUKUSUYOSETSUCHAKUZAISHIITOOYOBI HISANKABUTSUSERAMITSUKUSUYOSETHICHAKUTSUUSERAMITSUKUSUNOSETSUCHAKUHOHO

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14723485A JPH0240027B2 (en) 1985-07-04 1985-07-04 HISANKABUTSUSERAMITSUKUSUYOSETSUCHAKUZAISHIITOOYOBI HISANKABUTSUSERAMITSUKUSUYOSETHICHAKUTSUUSERAMITSUKUSUNOSETSUCHAKUHOHO

Publications (2)

Publication Number Publication Date
JPS627678A JPS627678A (en) 1987-01-14
JPH0240027B2 true JPH0240027B2 (en) 1990-09-10

Family

ID=15425605

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14723485A Expired - Lifetime JPH0240027B2 (en) 1985-07-04 1985-07-04 HISANKABUTSUSERAMITSUKUSUYOSETSUCHAKUZAISHIITOOYOBI HISANKABUTSUSERAMITSUKUSUYOSETHICHAKUTSUUSERAMITSUKUSUNOSETSUCHAKUHOHO

Country Status (1)

Country Link
JP (1) JPH0240027B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3627358B2 (en) * 1996-03-26 2005-03-09 株匏䌚瀟豊田自動織機 Single side swash plate compressor

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JPS627678A (en) 1987-01-14

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