JPH02213458A - Method for sealing thermally sprayed ceramic material - Google Patents
Method for sealing thermally sprayed ceramic materialInfo
- Publication number
- JPH02213458A JPH02213458A JP3378289A JP3378289A JPH02213458A JP H02213458 A JPH02213458 A JP H02213458A JP 3378289 A JP3378289 A JP 3378289A JP 3378289 A JP3378289 A JP 3378289A JP H02213458 A JPH02213458 A JP H02213458A
- Authority
- JP
- Japan
- Prior art keywords
- monomer
- pores
- reduced pressure
- under reduced
- pressure
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims abstract description 19
- 238000007789 sealing Methods 0.000 title claims description 16
- 229910010293 ceramic material Inorganic materials 0.000 title abstract description 5
- 239000000463 material Substances 0.000 claims abstract description 37
- 239000000178 monomer Substances 0.000 claims abstract description 33
- 239000011148 porous material Substances 0.000 claims abstract description 33
- 239000002685 polymerization catalyst Substances 0.000 claims abstract description 10
- 238000010438 heat treatment Methods 0.000 claims abstract description 5
- 230000000379 polymerizing effect Effects 0.000 claims abstract description 3
- 239000000919 ceramic Substances 0.000 claims description 22
- 239000007921 spray Substances 0.000 claims description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract description 22
- 230000007797 corrosion Effects 0.000 abstract description 10
- 238000005260 corrosion Methods 0.000 abstract description 10
- 239000004342 Benzoyl peroxide Substances 0.000 abstract description 6
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract description 6
- 235000019400 benzoyl peroxide Nutrition 0.000 abstract description 6
- 238000006116 polymerization reaction Methods 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 12
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- 238000005507 spraying Methods 0.000 description 10
- 238000010586 diagram Methods 0.000 description 9
- 238000000576 coating method Methods 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 7
- 238000001704 evaporation Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 4
- 238000007751 thermal spraying Methods 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000001291 vacuum drying Methods 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Coating By Spraying Or Casting (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はセラミック溶射が適用される製品の封孔処理方
法に関し、特に軸流ファン翼、コンデVツサ翼などの可
動翼ポンプのフンナペーンの製作に有利に適用すること
ができる方法に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a method for sealing a product to which ceramic spraying is applied, and in particular to the production of a funnel for a movable vane pump such as an axial fan blade or a V-shape blade. Concerning a method that can be advantageously applied to.
セフミックの溶射材は耐摩耗性に優れた材料であシ、最
近各種製品に利用されている。Cefmic's thermal spray material has excellent wear resistance and has recently been used in various products.
例えば、最近可動翼ポンプは流体輸送の負荷変動追従制
御運転が容易に行える特徴を活かして多用されるようセ
なってきているが、土砂、アッVユ、その低化合物の結
晶を含むスラリ溶液の輸送において、可動翼が激しく摩
耗する問題をしばしば生じている。このため、従来から
耐摩耗性及び耐食性に優れた材料の選定が強く望まれて
いるが、耐摩耗性に優れた材料が必ずしも耐食性を満足
せず、逆に耐食性に優れた材料が耐摩耗性を満足しない
といった環境も多く、腐食、摩耗の問題が解決されてい
ないのが現状状であシ、これに対して、従来、耐摩耗性
を満足しなかった材料の接液部の表面にセラミック溶射
を施こし、耐摩耗性を改蕾するといった方法が提案され
ている。For example, movable vane pumps have recently come into widespread use due to their ability to easily perform load fluctuation follow-up control operations for fluid transport. In transportation, the problem of severe wear of movable wings often arises. For this reason, it has been strongly desired to select materials with excellent wear resistance and corrosion resistance.However, materials with excellent wear resistance do not necessarily satisfy corrosion resistance, and conversely, materials with excellent corrosion resistance have high wear resistance. There are many environments where the wear resistance is not satisfied, and the current situation is that the problems of corrosion and wear have not been solved. A method of thermal spraying to improve wear resistance has been proposed.
しかしながら、現状開発されている溶射技術では無細孔
の皮膜が得られず、耐食性が要求される製品への応用が
阻れている。これを解決するため、従来から溶射層[K
生じた細孔を封じる、謂ゆる封孔処理方法が提案されて
いる。However, currently developed thermal spraying techniques cannot produce pore-free coatings, which prevents them from being applied to products that require corrosion resistance. To solve this problem, conventional thermal sprayed layers [K
A so-called pore sealing treatment method has been proposed to seal the generated pores.
従来、提案されている封孔処理方法はエポキシ樹脂、ポ
リエステ〃系樹脂、シリコーン系樹脂などの熱硬化性樹
脂又はアクリル樹脂、酢酸ビニル樹脂のエマルジョンを
塗布する方法あるいはそれらの樹脂を希釈した溶液に浸
漬して含浸させる方法がある。Conventionally, proposed pore sealing methods include applying emulsions of thermosetting resins such as epoxy resins, polyester resins, and silicone resins, acrylic resins, and vinyl acetate resins, or applying diluted solutions of these resins. There is a method of soaking and impregnating.
従来の樹脂溶液の塗布あるいは含浸させる方法において
、樹脂の希釈率を小さくした場合は溶液の粘度が高くな
るため溶射皮膜の細孔内に入シに<(、溶射層の極く表
層を覆っているだけの状態になシ易く、又、逆に希釈率
を大きくした場合には細孔の奥深(まで入シ易くなるが
、乾燥により溶媒が揮散後は細孔内に再び穴ができ、細
孔内全体を樹脂で埋めた状態にはなり難いなどの問題が
あり、従来から封孔処理をしたセラミック溶射材であっ
ても、水溶液と接触する環境では溶射セラミックと母材
との界面が腐食され、長期耐久性が要求されるような製
品には適用し難い。In the conventional method of applying or impregnating a resin solution, if the dilution rate of the resin is reduced, the viscosity of the solution increases, so it may not penetrate into the pores of the sprayed coating, and may not cover the very surface layer of the sprayed layer. On the other hand, if the dilution rate is increased, it becomes easier to penetrate deep into the pores, but after the solvent evaporates due to drying, holes are formed in the pores again, There are problems such as it being difficult to fill the entire hole with resin, and even with conventionally sealed ceramic sprayed materials, the interface between the sprayed ceramic and the base material corrodes in an environment where it comes into contact with an aqueous solution. Therefore, it is difficult to apply it to products that require long-term durability.
本発明は上記技術水準に鑑み、セフミック溶射材の封孔
処理方法における従来の欠点を解消し、セフミック溶射
材の細孔を完全に樹脂で封じ込め、腐食性液体の浸透を
防止できる耐食性に優れ九封孔処理方法を提供しようと
するものである。In view of the above-mentioned state of the art, the present invention eliminates the conventional drawbacks in the pore sealing method for Cefmic thermal spraying materials, completely seals the pores of Cefmic thermal spraying materials with resin, and provides excellent corrosion resistance that prevents the penetration of corrosive liquids. The present invention attempts to provide a method for sealing.
本発明は、セラミック溶射材の封孔処理を行うに際し、
セフミック溶射材を加温しながら減圧乾燥する第一工程
、
減圧を保持し良状態で、モノマーをフラッシュさせて該
溶射材の細孔にモノマーを吸着させる第二工程、
減圧状態を保持した状態で、モノマーに重合触媒を混合
した溶液を該溶射材の細孔内に含浸させる第三工程、
前記モノマーに重合触媒を混合した溶液を含浸した溶射
材のモノマーを、化ツマー蒸気が温度、圧力に対して平
衡な分圧下において重合させる第四工程
からなることを特徴とするセラミック溶射材の封孔処理
方法である。When performing pore sealing treatment on ceramic sprayed materials, the present invention involves the first step of drying the cefmic sprayed material under reduced pressure while heating it, and the monomer is flashed into the pores of the sprayed material while maintaining reduced pressure and in good condition. A second step of adsorbing the monomer; A third step of impregnating the pores of the thermal spray material with a solution of a mixture of monomers and a polymerization catalyst while maintaining a reduced pressure state; Impregnating the monomer with a solution of a mixture of a polymerization catalyst. This is a method for sealing a ceramic thermal sprayed material, which comprises a fourth step of polymerizing the monomer of the thermal sprayed material under a partial pressure in which the chemical vapor is in equilibrium with the temperature and pressure.
本発明におけるセラミック溶射材としては、アルミナ、
タングステンカーバイド、ジルコニア、チタニアなど多
くの耐摩耗性に優れたセラミック材ならば何んでも使用
できる。また化ツマ−としてはスチレン、メチルメタア
クリレートなど多くのものが使用でき、重合触媒として
もベンゾイルパーオキサイド、バークミルパーオキサイ
ドなど多くの有機過酸化物が使用できる。なお重合触媒
の混合量は製品の種類によって任意に選定できるが、好
ましくは15〜!L。The ceramic spraying material in the present invention includes alumina,
Any highly wear-resistant ceramic material can be used, including tungsten carbide, zirconia, titania, and many others. Furthermore, many compounds such as styrene and methyl methacrylate can be used as the chemical compound, and many organic peroxides such as benzoyl peroxide and bark mill peroxide can be used as the polymerization catalyst. The mixing amount of the polymerization catalyst can be arbitrarily selected depending on the type of product, but preferably 15~! L.
vtlの範囲の量で使用される。Used in amounts ranging from vtl.
本発明は微細な細孔の奥深くまで樹脂を完全に充填する
ため、第一工程において細孔内に吸着した水分を完全に
除去する目的で加温し表から減圧乾燥を行う。もし水分
が残留した場合にはモノマー含浸工程において、モノマ
ーを細孔全体に充填するのを阻害するばかりでなく、セ
ラミックとモノマーとの濡れを阻害するため、モノマー
を含浸させて重合させた場合、セラミックと樹脂とが接
着した状態になりにくい。In the present invention, in order to completely fill the resin deep into the fine pores, in the first step, the resin is heated and dried under reduced pressure from the surface in order to completely remove the moisture adsorbed in the pores. If moisture remains, it will not only prevent the monomer from filling all the pores in the monomer impregnation process, but also inhibit wetting of the ceramic and the monomer, so if the monomer is impregnated and polymerized, It is difficult for the ceramic and resin to form an adhesive state.
第二の工程は化ツマ−を細孔内に含浸させやすくするた
めの処理で、減圧した状態でモノマーをフラッシュさせ
て、細孔内にモノマーの蒸気を導入するととにより、細
孔内のセラミック面を化ツマ−で濡らす工程である。こ
の工程によシ、次工程のモノマー含浸を完全にする作用
をするばかりでなく、化ツマ−を重合した樹脂とセラミ
ックの接着を強め、細孔を完全に封孔できるのである。The second step is a treatment to facilitate the impregnation of the chemical into the pores.The monomer is flashed under reduced pressure and the monomer vapor is introduced into the pores. This is the process of wetting the surface with soap. This step not only serves to complete the monomer impregnation in the next step, but also strengthens the adhesion between the polymerized resin and the ceramic, thereby completely sealing the pores.
第三の工程は、重合触媒を混合した化ツマ−を含浸させ
る工程である。セラミック溶射材を重合触媒を混合した
七ツマー溶液に完全に浸漬させて減圧することにより、
セラミック溶射材の細孔部に重合触媒を混合したモノマ
ーを含浸させることができる。The third step is a step of impregnating a polymer mixed with a polymerization catalyst. By completely immersing the ceramic spray material in a 7-mer solution containing a polymerization catalyst and reducing the pressure,
The pores of the ceramic thermal spray material can be impregnated with a monomer mixed with a polymerization catalyst.
第四の工程は、セラミック溶射材の細孔部に含浸したモ
ノマーを蒸発揮散させることなく、すべて重合させる工
程である。含浸した化ツマ−を蒸発揮散させないために
、モノマーの蒸気が含浸したモノマーを重合させる温度
、圧力において平衡な分圧に調斃した容器内に移し、重
合が完結する迄保持するのがよい。The fourth step is a step in which all of the monomer impregnated into the pores of the ceramic thermal spray material is polymerized without evaporation or diffusion. In order to prevent the impregnated polymer from evaporating and evaporating, it is preferable to transfer the monomer vapor into a container whose partial pressure is adjusted to equilibrium at the temperature and pressure at which the monomer is polymerized, and to hold the container until the polymerization is completed.
以上、第一工程から第四工程まで連続的に処理すること
により、セラミック溶射材の細孔内を完全に封じること
ができ、耐食性に優れたセラミック溶射材を提供できる
。By carrying out the continuous treatment from the first step to the fourth step as described above, the pores of the ceramic sprayed material can be completely sealed, and a ceramic sprayed material with excellent corrosion resistance can be provided.
以下、本発明の一実施例を第1図〜第8図を参照しなが
ら詳述する。Hereinafter, one embodiment of the present invention will be described in detail with reference to FIGS. 1 to 8.
第1図、第2図は可動翼ポンプのランナベーンの一態様
を示す図で、第1図はポンプ本体に取付ける軸に対して
正面から見た図、第2図は軸に対して上から見た図であ
る。第5図はランナベーンの軸部を除いた全面に500
μmの厚さにアルミナを溶射したランナベーンを軸に対
して上から見た図、第4図は第3図のA−に矢視の一部
の断面を拡大した図である。Figures 1 and 2 are views showing one aspect of the runner vane of a movable vane pump. Figure 1 is a front view of the shaft attached to the pump body, and Figure 2 is a view of the shaft from above. This is a diagram. Figure 5 shows a 500mm coating on the entire surface of the runner vane excluding the shaft.
FIG. 4 is an enlarged view of a cross section taken in the direction of the arrow A- in FIG.
第5図〜第8図はアルミナを溶射したランナベーンをス
チレンモノマーを用いて封孔処理スる態様を示す図であ
り、第5図は溶射したランナベーンの減圧乾燥工程の態
様を示す図、第6図ハスチレンモノマ一のフラッシュに
よるアルミナ溶射コーティング膜細孔内ヘモツマを吸着
させる態様を示す図、第7図はスチレンモノマーに重合
触媒としてベンゾイルパーオキサイドをs wt4加え
た溶液中にアルミナ溶射したランナベーンを浸漬し、減
圧状態でベンゾイルパーオキサイドを含むスチレンモノ
マーを含浸する態様を示す図、第8図はスチレンモノマ
ー蒸気中でアルミナ溶射ランナベーンのコーテイング膜
細孔内に含浸したモノマーを重合させる態様を示す図で
ある。Figures 5 to 8 are diagrams showing how runner vanes sprayed with alumina are sealed using styrene monomer; Figure 5 is a diagram showing how the sprayed runner vanes are dried under reduced pressure; Figure 7 shows a method of adsorbing hemotsma in the pores of an alumina thermal spray coating film using a flash of hastyrene monomer. Figure 8 shows an embodiment in which the styrene monomer containing benzoyl peroxide is impregnated in a reduced pressure state by immersion, and Figure 8 shows an embodiment in which the monomer impregnated into the pores of the coating membrane of an alumina thermal spray runner vane is polymerized in styrene monomer vapor. It is.
第1図〜第8図の図において、1は可動翼ポンプのラン
ナーベーン本体(日as141Ell)、2はランナベ
ーン先端部に溶射したアルミナ溶射コーテイング膜、3
は蓋付減圧容器、4はコック付モノマー注入器、5はコ
ック、6は真空ポンプ、7はベンゾイルパーオキサイド
を含むスチレンモノマーのi液、8はスチレンモノマー
の蒸気、9はスチレンモノマー蒸発用容器である。1 to 8, 1 is the runner vane body of the movable vane pump (Japanese AS141Ell), 2 is the alumina spray coating film sprayed on the tip of the runner vane, 3
is a vacuum container with a lid, 4 is a monomer injector with a cock, 5 is a cock, 6 is a vacuum pump, 7 is a styrene monomer i-liquid containing benzoyl peroxide, 8 is a styrene monomer vapor, 9 is a styrene monomer evaporation container It is.
最長部の長さ400−のランナーベーン先端部にアルミ
ナを500μm溶射したランナーベーンを作製し、その
ランナベーンを100℃に加熱したのち、真空ボンデ6
で減圧できるようにした容器3内に入れ、100℃に加
温しながら、1トー〜で10分間減圧乾燥した。(第5
図)
次いで、減圧を保持した状態で、温度を室温まで下げた
のち、あらかじめ容器3上部にセットしたスチレンモノ
マー注入器4のコック5を開き、溶射コーテイング膜の
面にスチレンのモノマーが接触しないようにフラッシュ
させ、その後、真空ポンプ6につながるコック5を閉じ
て10分間保持した。(第6図)
次いで、モノマー注入器4内にベンゾイルパーオキサイ
ド3 wt4を含むスチレンモノマーを入れ、真空ボン
デ6につながるコック5を開いて容器内を減圧にしなが
ら、スチレンモノマー注入器4のコック5を開いて、供
試ランナベーンのアルミナ溶射コーティング部の全体が
完全に浸漬するまで、ベンゾイルパーオキサイド3yt
4を含むスチレンモノマーを注入し九のち、減圧しなが
ら10分間保持した。(第7図)次いで、減圧を解除し
たのち、ランナーベーンを取り出し、スチレンモノマー
を入れた蒸発用容器9を設置した蓋付容器3に移し、5
0Cで24時間保持した。(第8図)
上記、処理を行ったアμミナ溶射フンナベーンと、封孔
処理を行なわセかったアルミナ溶射ランナベーン及び常
温硬化エポキシ樹脂を表面に塗布したアルミナ溶射ラン
ナベーンを可動翼ポンプに取付け、pHaoの硫酸溶液
を循環させながら、6ケ月間耐久性評価試験を行った結
果、上記封孔処理を行ったランナベーンは接着面の異常
は認められなかったのに対し、封孔処理をしなかったも
の及びエポキシ樹脂を塗布したものはコーティング嘆と
母材の接着面から剥離した。A runner vane was prepared by thermally spraying alumina to a thickness of 500 μm on the tip of the runner vane with a length of 400 mm at the longest part, and after heating the runner vane to 100 °C, it was vacuum bonded to 6
The sample was placed in a container 3 capable of being depressurized, and dried under reduced pressure of 1 tor for 10 minutes while heating to 100°C. (5th
Figure) Next, while maintaining the reduced pressure, the temperature was lowered to room temperature, and then the cock 5 of the styrene monomer injector 4, which had been set in advance on the top of the container 3, was opened to prevent the styrene monomer from coming into contact with the surface of the thermally sprayed coating film. After that, the cock 5 connected to the vacuum pump 6 was closed and held for 10 minutes. (Fig. 6) Next, styrene monomer containing benzoyl peroxide 3wt4 is put into the monomer injector 4, and while the cock 5 connected to the vacuum bonder 6 is opened to reduce the pressure inside the container, the cock 5 of the styrene monomer injector 4 is opened. Open the test runner vane and add 3 yt of benzoyl peroxide until the entire alumina spray coating part of the test runner vane is completely immersed.
A styrene monomer containing 4 was injected, and after 9 hours, the mixture was held for 10 minutes under reduced pressure. (Fig. 7) Next, after releasing the reduced pressure, the runner vane was taken out and transferred to a lidded container 3 equipped with an evaporation container 9 containing styrene monomer.
It was kept at 0C for 24 hours. (Fig. 8) Attach the Amu Mina thermal sprayed runner vane that has undergone the above treatment, the alumina thermal sprayed runner vane that has not been subjected to the sealing treatment, and the alumina thermal sprayed runner vane whose surface is coated with room temperature curing epoxy resin to a movable vane pump. As a result of conducting a durability evaluation test for 6 months while circulating a sulfuric acid solution, no abnormality was observed on the adhesive surface of the runner vane that had undergone the above sealing treatment, whereas the runner vane that had not undergone the sealing treatment And those coated with epoxy resin peeled off from the adhesive surface of the coating and base material.
実施例Iと同様の操作で、スチレンモノマーをメチルメ
タアクリレートモノマーにかえて、封孔処理を行なった
供試セラミック溶射材を作成した。これを実施例■と同
条件で腐食試験した結果、スチレンモノマーで封孔処理
したのと同様、良好な1耐食性を示した。A sample ceramic sprayed material was prepared in the same manner as in Example I except that the styrene monomer was replaced with methyl methacrylate monomer and the pores were sealed. This was subjected to a corrosion test under the same conditions as in Example (2), and as a result, it showed good corrosion resistance (1), similar to that obtained by sealing with styrene monomer.
本発明は従来セラミック溶射材が適用で舞なかった腐食
性環境までセラミック溶射材を適用できるようにしたも
ので、耐摩耗性が要求されるあらゆる製品にセラミック
溶射材を適用可能にした工業的効果は大きい。The present invention enables ceramic spraying materials to be applied to corrosive environments where conventional ceramic spraying materials could not be applied, and has the industrial effect of making ceramic spraying materials applicable to all products that require wear resistance. is big.
第1図、第2図は可動翼ランナベーンの態様を示す図、
第5図はランナベーンの一部にセラミック溶射した態様
を示す図、第4図は第3図のA −A’矢視の一部の断
面の拡大図、第5図〜第8図は封孔処理方法の態様を示
す図でsb、第5図は溶射し°たランナベーンの減圧乾
燥工程の態様を示す図、第6図はスチレンモノマーのフ
ラッシュによるアルミナ溶射コーティング膜細孔内ヘモ
ツマ−を吸着させる態様を示す図、第7図はスチレンモ
ノマーに重合触媒としてペンシイ〃パーオキサイドS
wt4加えた溶液中にアルミナ溶射したランナベーンを
浸漬し、減圧状態でペンシイ〃パーオキサイドを含むス
チレンモノマーを含浸する態様を示す図、第8図はスチ
レンモノマー蒸気中でアルミナ溶射ランナベーンのコー
テイング膜細孔内に含浸したモノマーを重合させる態様
を示す図である。
第1図Figures 1 and 2 are diagrams showing aspects of the movable blade runner vane;
Fig. 5 is a diagram showing a state in which ceramic spraying is applied to a part of the runner vane, Fig. 4 is an enlarged view of a cross section taken along arrow A-A' in Fig. 3, and Figs. 5 to 8 are sealing holes. Figure 5 is a diagram showing an aspect of the treatment method, Figure 5 is a diagram showing an aspect of the vacuum drying process of the thermally sprayed runner vane, and Figure 6 is a diagram showing the aspect of the vacuum drying process of the thermally sprayed runner vane, and Figure 6 is the adsorption of hemotsma in the pores of the alumina thermally sprayed coating film by flashing styrene monomer. A diagram showing an embodiment, Figure 7 shows the addition of Pencil Peroxide S to styrene monomer as a polymerization catalyst.
Figure 8 shows the coating film pores of the alumina sprayed runner vane in the styrene monomer vapor by immersing the alumina sprayed runner vane in a solution containing wt4 and impregnating it with styrene monomer containing pencil peroxide under reduced pressure. It is a figure which shows the aspect which polymerizes the monomer impregnated in the inside. Figure 1
Claims (1)
溶射材を加温しながら減圧乾燥する第一工程、 減圧を保持した状態で、モノマーをフラツシュさせて該
溶射材の細孔にモノマーを吸着させる第二工程、 減圧状態を保持した状態で、モノマーに重合触媒を混合
した溶液を該溶射材の細孔内に含浸させる第三工程、 前記モノマーに重合触媒を混合した溶液を含浸した溶射
材のモノマーを、モノマー蒸気が温度、圧力に対して平
衡な分圧下において重合させる第四工程 からなることを特徴とするセラミツク溶射材の封孔処理
方法。[Claims] When sealing the ceramic sprayed material, the first step is to dry the ceramic sprayed material under reduced pressure while heating it, and while the reduced pressure is maintained, the monomer is flashed to close the pores of the sprayed material. a second step in which the monomer is adsorbed on the thermal spray material; a third step in which the pores of the thermal spray material are impregnated with a solution in which the monomer is mixed with a polymerization catalyst while maintaining a reduced pressure state; A method for sealing a ceramic thermal spray material, comprising a fourth step of polymerizing the impregnated monomer of the thermal spray material under a partial pressure where the monomer vapor is in equilibrium with temperature and pressure.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1033782A JP2647482B2 (en) | 1989-02-15 | 1989-02-15 | Sealing treatment method for ceramic spray coating |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1033782A JP2647482B2 (en) | 1989-02-15 | 1989-02-15 | Sealing treatment method for ceramic spray coating |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02213458A true JPH02213458A (en) | 1990-08-24 |
JP2647482B2 JP2647482B2 (en) | 1997-08-27 |
Family
ID=12396037
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1033782A Expired - Fee Related JP2647482B2 (en) | 1989-02-15 | 1989-02-15 | Sealing treatment method for ceramic spray coating |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2647482B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2305672A (en) * | 1995-09-29 | 1997-04-16 | Aea Technology Plc | An electrically isolating support for electronic components |
GB2397257A (en) * | 2003-01-16 | 2004-07-21 | Rolls Royce Plc | Article provided with a vibration damping coating |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01263259A (en) * | 1988-04-15 | 1989-10-19 | Mitsubishi Heavy Ind Ltd | Sealing treatment for ceramic thermally sprayed material |
-
1989
- 1989-02-15 JP JP1033782A patent/JP2647482B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01263259A (en) * | 1988-04-15 | 1989-10-19 | Mitsubishi Heavy Ind Ltd | Sealing treatment for ceramic thermally sprayed material |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2305672A (en) * | 1995-09-29 | 1997-04-16 | Aea Technology Plc | An electrically isolating support for electronic components |
GB2397257A (en) * | 2003-01-16 | 2004-07-21 | Rolls Royce Plc | Article provided with a vibration damping coating |
Also Published As
Publication number | Publication date |
---|---|
JP2647482B2 (en) | 1997-08-27 |
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