JPH01281A - overlay coating - Google Patents
overlay coatingInfo
- Publication number
- JPH01281A JPH01281A JP63-70831A JP7083188A JPH01281A JP H01281 A JPH01281 A JP H01281A JP 7083188 A JP7083188 A JP 7083188A JP H01281 A JPH01281 A JP H01281A
- Authority
- JP
- Japan
- Prior art keywords
- coating
- weight
- particles
- protective layer
- particle size
- 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
- 238000000576 coating method Methods 0.000 title claims description 33
- 239000011248 coating agent Substances 0.000 title claims description 23
- 239000002245 particle Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 13
- 239000011241 protective layer Substances 0.000 claims description 11
- 238000009826 distribution Methods 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- 239000000853 adhesive Substances 0.000 claims description 6
- 230000001070 adhesive effect Effects 0.000 claims description 6
- 238000005137 deposition process Methods 0.000 claims description 6
- 238000005507 spraying Methods 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 239000002131 composite material Substances 0.000 claims description 3
- 230000008021 deposition Effects 0.000 claims description 3
- 239000011159 matrix material Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 2
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 2
- 239000011819 refractory material Substances 0.000 claims description 2
- 229910052727 yttrium Inorganic materials 0.000 claims description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical group [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 11
- 230000004888 barrier function Effects 0.000 description 10
- 238000007747 plating Methods 0.000 description 7
- 239000010410 layer Substances 0.000 description 5
- 229910017052 cobalt Chemical group 0.000 description 3
- 239000010941 cobalt Chemical group 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical group [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 238000004873 anchoring Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000010285 flame spraying Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000005382 thermal cycling Methods 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
- 229910001233 yttria-stabilized zirconia Inorganic materials 0.000 description 1
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 description 1
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、支持体上に熱障壁を結合するオーバレイ・コ
ーティングの提供に関する。上記のオーバレイ・コーテ
ィングは、特に腐食や浸食が発生しそうな高温環境にさ
らされる構成部分に用いられるが、上記コーティングの
主要な、但し必ずしも唯一ではない応用は、ガスタービ
ン・エンジンの部品、特にガスタービンの燃焼筒製品、
静翼および動翼、ならびに案内羽根に対するものである
。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to the provision of overlay coatings that bond thermal barriers onto substrates. Although the above-mentioned overlay coatings are particularly used on components exposed to high temperature environments where corrosion and erosion are likely to occur, the primary, but not necessarily the only, application of the above-mentioned coatings is on components of gas turbine engines, especially gas Turbine combustion tube products,
This applies to stationary blades, rotor blades, and guide vanes.
従来の技術
適宜に作られた支持体表面に、プラズマ析出プロセスを
用いて、MCrAj!Y (ここにMはニッケルもしく
はコバルト、またはニッケルおよびコバルトなどの適当
な金属)から成る保護層を最初に噴霧コーティングし、
次いで保護か内のそれよりも可成り粗大な粒子を析出物
内に生成するフレーム析出ブOセスにより金属から成る
固着層を噴霧コーティングし、次いでプラズマ析出プロ
゛セスにより耐火物から成る熱障壁を噴霧コーティング
することによってオーバレイ・コーティングを生成する
ことが提案されている。Conventional Techniques Using a plasma deposition process on a suitably prepared support surface, MCrAj! first spray coating a protective layer consisting of Y (where M is nickel or cobalt, or a suitable metal such as nickel and cobalt);
A bonded layer of metal is then spray coated by a flame deposition process which produces significantly coarser particles in the deposit than those in the protective barrier, and then a thermal barrier of refractory is coated by a plasma deposition process. It has been proposed to produce overlay coatings by spray coating.
発明が解決しようとする問題点
この手順は概して申し分のないものであるが、これには
若干の理想的でない面がある。例えば、複雑で内的する
表面に対するフレーム噴霧は困難且つ高価となる可能性
がある。PROBLEM SOLVED BY THE INVENTION Although this procedure is generally satisfactory, it has some non-ideal aspects. For example, flame spraying complex internal surfaces can be difficult and expensive.
問題点を解決するための手段
本発明によれば、CrA1M2の粒子を包含する金属マ
トリックスM 〈ここにMlはNiもしくはCoまたは
その両者、M2はy、si、T;、Hf、 Taまたは
希土類元素の内−つ以上〉の複合の電解または無電解析
出により保護層を形成し、保FillのCrAiM2の
粒子より大きい粒度の粒子を包含する金属マトリックス
の複合の電解または無電解析出により固着被覆を形成し
、次いでプラズマ析出プロセスにより耐火物から成る熱
障壁を噴霧コーティングすることにより、支持体上のオ
ーバレイ・コーティングが得られる。Means for Solving the Problems According to the invention, a metal matrix M containing particles of CrA1M2 (where Ml is Ni or Co or both, M2 is y, si, T; Hf, Ta or a rare earth element) forming a protective layer by electrolytic or electroless deposition of a composite of one or more of The overlay coating on the support is then obtained by spray coating a thermal barrier of refractory material by a plasma deposition process.
従って本発明は、保護層と固着被覆とが何れも、フレー
ム噴霧されるのではなく、めっきされる、という点にお
いて、さきに提案されたそれとは異なるものである。The present invention thus differs from those previously proposed in that both the protective layer and the bonding coating are plated rather than flame sprayed.
めっきによるM CrAIM2層の生成は、あす
る段階で熱処理により修正されるコーティングを生成す
ることを目的とするGB−2,167,446−Aに既
に提案されており、その明細書は粒度の綿密な制御がな
されるべきことを強調しており、概括的に提示された粒
度の要件は、析出されたコーティング内の粒子の少なく
とも99(重量)%が25μm未満または少なくとも9
5%が3.0〜13.6μ卯である、としている。同明
細書には電着により極めて望ましい表面仕上がりを有す
るコーティングが生成される、と述べである。めっきは
、滑らかな、光沢さえある、表面を備えたコーティング
を生成することで周知されており、この粒度の粒子の析
出されたマトリックスへの結合によって比較的滑らかな
表面が更にもたらされる。噴霧されたMCr/M!Yコ
ーティングは不適切なことに表面が荒いので、充分な付
着性を以て、熱障壁を、噴霧コーティングされたMCr
AjYコーティングへ直接に付着させることはできない
。粗い粒子を用いて噴霧コーティングされた固着被覆が
必要とされていた。従って、熱障壁の素地を用意する際
、複合めっきは全く無用であろうと考・えられる。しか
し、最も驚いたことには、より大きい粒子を含むめっき
された固着被覆を後続させた、めっきされた
M CrAIM2被覆によってib満足な素地が得られ
、その上に、層間に全く充分な付着性を保ちながら、噴
霧コーティングにより熱障壁を付着させ得ることが見い
だされたのである。このように、めっきされた固着層は
、荒い定着面を生成するために用いられるが、これは、
平滑度の一つである普通に容認されるめっきされた被覆
の性質と全く反対の何かである。The production of M CrAIM2 layers by plating has already been proposed in GB-2,167,446-A, which aims to produce coatings that are subsequently modified by heat treatment, the specification of which It emphasizes that strict control must be exercised, and the generally proposed particle size requirements are such that at least 99% (by weight) of the particles in the deposited coating are less than 25 μm or at least 9
It is said that 5% is between 3.0 and 13.6 μm. The specification states that electrodeposition produces coatings with highly desirable surface finishes. Plating is well known for producing coatings with smooth, even glossy surfaces, and the bonding of particles of this size to the deposited matrix further provides a relatively smooth surface. Sprayed MCr/M! Since the Y coating has an undesirably rough surface, a thermal barrier with sufficient adhesion can be achieved by spray-coated MCr.
It cannot be applied directly to the AjY coating. A bonded coating was needed that was spray coated with coarse particles. Therefore, it is thought that composite plating would be completely unnecessary when preparing the substrate for the thermal barrier. Most surprisingly, however, a plated M CrAIM2 coating followed by a plated adherent coating containing larger particles yielded an ib satisfactory substrate, and on top of that there was quite sufficient adhesion between the layers. It has now been discovered that the thermal barrier can be applied by spray coating while maintaining the thermal barrier properties. Thus, a plated anchoring layer is used to create a rough anchoring surface, which
This is something quite contrary to the commonly accepted property of plated coatings, which is one of smoothness.
固着被覆の好適な構成要素は保護層のそれと同一または
それに類似しているがそれは、固着機能を備えることに
加えて、下履をなす保M層が設けられるためのそれと同
様な作動条件にこの被覆がさらされるためである。Preferred components of the adhesive coating are the same as or similar to those of the protective layer, which, in addition to providing an adhesive function, is suitable for operating conditions similar to those for which the retention layer of the undergarment is provided. This is because the coating is exposed.
保護層を付着させるための好適な構成要素ならびにその
方法は、前述のGB−2,167,446−Aに記述さ
れたそれらであり、使用され得る装置および方法の更に
詳細については、GB−2゜014.189−Aおよび
US−4,305,792を参照されたい。上記の装置
および方法は、固着被覆を付着させるために使用するこ
とができる。Suitable components and methods for applying the protective layer are those described in GB-2,167,446-A, supra; further details of the apparatus and methods that may be used can be found in GB-2 See 014.189-A and US-4,305,792. The apparatus and method described above can be used to apply bond coatings.
実施例および作用
本発明は種々の方法で実施できるが、ここで例示のため
、ガス・タービン買上の一つの特定のオーバレイの装置
について説明する。DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS AND OPERATION Although the present invention may be implemented in a variety of ways, one particular overlay arrangement on a gas turbine will now be described for purposes of illustration.
翼は先ず、めっきに適した準備処理を施され、一つの例
ににあっては、それが2分間、シアン化物の洗浄剤に浸
せきされ、水洗がこれに続き、塩化第二鉄エッチ液内で
の30秒間の浸せきによりエツチングされ、水洗がこれ
に続き、1dm2当たり3.5Aの電流密度で3分間、
ニッケル浴゛に置くことによりニッケル・ストライクを
施される。The wing is first subjected to a suitable preparation process for plating; in one example, it is soaked in a cyanide cleaner for two minutes, followed by a water rinse, and then soaked in a ferric chloride etch solution. Etched by immersion in water for 30 seconds, followed by rinsing with water for 3 minutes at a current density of 3.5 A per dm2.
A nickel strike is applied by placing it in a nickel bath.
次いで翼は、GB−2,014,189−8に記述され
ためつき用バレル内に保持され、陰極接点に接続される
。GB−2,014,189−Bに記述された技法を用
いて0.076〜0.127閲の厚さにCoN1CrA
IYのコーティングが舅に施されるが、バスはCON
iめっき液を包含し、粒子は重1rcr60SAi40
.Y1.7の割合のものを含むCrAj!Yである。粒
度分布は、5μm未満で5(重量)%、10μm未満で
10〜15(重量)%、20μm未満で35〜55(重
量)%の最大値である。別の粒度分布は、5μ而未満で
7.7(重量)%、10μmで56(重量)%、20μ
m未満で94(重量)%、30μm未満で99(重量)
%の最大値である。The vane is then held in a tampering barrel as described in GB-2,014,189-8 and connected to the cathode contact. CoN1CrA to a thickness of 0.076 to 0.127 mm using the technique described in GB-2,014,189-B.
IY coating is applied to the father-in-law, but the bath is CON
i plating solution, the particles weigh 1rcr60SAi40
.. CrAj! containing a proportion of Y1.7! It is Y. The particle size distribution has a maximum of 5% (by weight) below 5 μm, 10-15% (by weight) below 10 μm, and 35-55% (by weight) below 20 μm. Another particle size distribution is 7.7% (wt) below 5μm, 56% (wt) below 10μm, 20μm
94 (weight)% for less than m, 99 (weight) for less than 30 μm
This is the maximum value of %.
保護層を備える舅は装置から取り外されて洗浄され、次
いで、同様のコバルトめっき液を包含し且つ保護層のた
めに用いたと同じ組成を有しながら後段に述べるような
異なる粒度分布を有するCrAj!Y粒子を装置に装入
した、英国特許出願第2182055号に記述された装
置内に定置される。最初のM、CrAxY被覆から第二
の定着被覆プロセス段階への移動に遅延が生ずると、構
成要素の表面は、塩化第二鉄エッチ液内での浸せきと最
初の前処理と同様なニッケル・ストライクとにより再活
性化される可能性がある。粒度分布は、150μ乳を超
える粒度については粉末の1%以下、38μm未満の粒
度については15%以下となるようになされる。めっき
は、0.025〜0.15Mの厚さを有する固着被覆を
生成するように行われる。The plate with the protective layer is removed from the apparatus and cleaned, then CrAj! containing the same cobalt plating solution and having the same composition as used for the protective layer but with a different particle size distribution as described below. It is placed in the apparatus described in UK Patent Application No. 2182055, in which Y particles are charged into the apparatus. If there is a delay in moving from the first M, CrAxY coating to the second fixed coating process step, the surface of the component will be immersed in a ferric chloride etch solution and a nickel strike similar to the first pretreatment. It may be reactivated by The particle size distribution is such that for particle sizes above 150 μm it is less than 1% of the powder and for particle sizes less than 38 μm it is less than 15% of the powder. Plating is carried out to produce a bonded coating with a thickness of 0.025-0.15M.
次いで、翼は取り外され、洗浄される。コーティングは
次いで、残余の析出物への表面の粉末の接着を行うため
、真空熱処理される。例えば翼を、1115℃で2時間
、もしくは1050〜1100℃の範囲内で2時間、ま
たは900〜1200℃の範囲内で、1200℃で最大
2時間もしくは900℃で最小1/4時間で、処理する
こともできる。次いで熱障壁が、プラズマ・フレーム析
出プロセスにより、固着被覆上に噴霧される。゛この被
覆は本質的に、重量で、7〜9%のY2O3、最大1.
5%のSi0 .0.5%のCaO10,3%のMob
、0.4%のFe2O3,0,2%のAl2O3および
0.2%のrho、、、それに残余がZrO2という化
学組成を有する8%イツトリア・スタビライズド・ジル
コニアから成る。粒度分布は、74μmを超える粒度に
ついでは最大10%、44μm超については65〜10
0%、44μm未満については最大25%となるように
なされる。真空熱処理を固着被覆の付着後に行う代りに
、それを熱障壁の付着後に同じ方法で行っても良い。The wings are then removed and cleaned. The coating is then vacuum heat treated to effect adhesion of the surface powder to the remaining deposit. For example, the blade may be treated at 1115°C for 2 hours, or in the range 1050-1100°C for 2 hours, or in the range 900-1200°C, for a maximum of 2 hours at 1200°C or a minimum of 1/4 hour at 900°C. You can also. A thermal barrier is then sprayed onto the bonded coating by a plasma flame deposition process. ``This coating consists essentially of 7-9% Y2O3 by weight, up to 1.
5% Si0. 0.5% CaO10.3% Mob
, 0.4% Fe2O3, 0.2% Al2O3 and 0.2% rho, . . . 8% yttria stabilized zirconia with the balance ZrO2. Particle size distribution is up to 10% for particle sizes greater than 74 μm and 65-10% for particle sizes greater than 44 μm.
0%, and for those less than 44 μm, the maximum is 25%. Instead of performing the vacuum heat treatment after depositing the adhesive coating, it may be performed in the same manner after depositing the thermal barrier.
GB−2,014,189−8に記述された方法に代わ
る方法として、本出願人等の英国特許出願第85265
46号(公告第2182055号)に記載の装置および
方法により保護層と固着被膜とを付着させることもでき
る。As an alternative to the method described in GB-2,014,189-8, our UK Patent Application No. 85265
The protective layer and the adhesive coating can also be applied by the apparatus and method described in No. 46 (Publication No. 2182055).
本発明による上述の方法で片側にコーティングされ、ま
た表面温度を2分間に1050℃に上昇させ且つ2分間
に下降させるためフレームの内外に動かされた、パドル
形試験片についての熱サイクル試験中、この試験片は、
代表的な商業上の容認レベルが500熱サイクルである
ところを、1000熱サイクルに充分に耐えたのである
。During thermal cycling tests on paddle-shaped specimens coated on one side with the method described above according to the invention and moved in and out of the frame to increase the surface temperature to 1050° C. for 2 minutes and decrease it for 2 minutes, This test piece is
It successfully withstood 1000 thermal cycles, where the typical commercially acceptable level is 500 thermal cycles.
Claims (4)
方法にして、 1)CrAlM_2の粒子を包含する金属マトリックス
M_1(ここにM_1はNiもしくはCoまたはその両
者、M_2はY、Si、Ti、Hf、Taまたは希土類
元素の内一つ以上)の複合の電解または無電解析出によ
り保護層を形成する段階と、 2)保護層のCrAlM_2の粒子より大きい粒度の粒
子を包含する金属マトリックスの複合の電解または無電
解析出により固着被覆を形成する段階と、 3)プラズマ析出プロセスにより耐火物から成る熱陣壁
を噴霧コーティングする段階とを含む方法。(1) A method of producing an overlay coating on a support, comprising: 1) a metal matrix M_1 containing particles of CrAlM_2, where M_1 is Ni or Co or both; M_2 is Y, Si, Ti, Hf; 2) forming a protective layer by electrolytic or electroless deposition of a composite of one or more of Ta or rare earth elements); 3) forming a bonded coating by electroless deposition; and 3) spray coating a thermal wall of refractory material by a plasma deposition process.
着被覆が、保護層の粒子より大きい粒度でありながら、
それと同じ組成であるようにした方法。(2) In the method according to claim 1, while the adhesive coating has a particle size larger than the particles of the protective layer,
How to make it have the same composition.
おいて、保護層の粒子の粒度分布が、5μm未満で5(
重量)%、10μm未満で10〜15(重量)%、20
μm未満で35〜55(重量)%の最大値を有するよう
にした方法。(3) In the method according to claim 1 or 2, the particle size distribution of the particles of the protective layer is less than 5 μm and 5 (
weight)%, 10 to 15 (weight)% less than 10 μm, 20
A method having a maximum value of 35 to 55% (by weight) below μm.
着被覆の粒子の粒度分布が、150μm超で1(重量)
%の最大値と、38μm未満で15(重量)%の最大値
とを有するようにした方法。(4) In the method according to claim 3, the particle size distribution of the particles of the adhesive coating is 1 (weight) when it exceeds 150 μm.
% and a maximum value of 15% (by weight) below 38 μm.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8706951 | 1987-03-24 | ||
GB878706951A GB8706951D0 (en) | 1987-03-24 | 1987-03-24 | Overlay coating |
Publications (3)
Publication Number | Publication Date |
---|---|
JPS64281A JPS64281A (en) | 1989-01-05 |
JPH01281A true JPH01281A (en) | 1989-01-05 |
JP2704878B2 JP2704878B2 (en) | 1998-01-26 |
Family
ID=10614510
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63070831A Expired - Lifetime JP2704878B2 (en) | 1987-03-24 | 1988-03-24 | Overlay coating |
Country Status (7)
Country | Link |
---|---|
US (1) | US4810334A (en) |
EP (1) | EP0288156B1 (en) |
JP (1) | JP2704878B2 (en) |
CA (1) | CA1324104C (en) |
DE (1) | DE3872294T2 (en) |
ES (1) | ES2032552T3 (en) |
GB (2) | GB8706951D0 (en) |
Families Citing this family (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2615871B1 (en) * | 1987-05-26 | 1989-06-30 | Snecma | SUPER-ALLOY TURBOMACHINE PARTS HAVING A METALLOCERAMIC PROTECTIVE COATING |
FR2638781B1 (en) * | 1988-11-09 | 1990-12-21 | Snecma | ELECTROPHORETIC ANTI-WEAR DEPOSITION OF THE CONSOLIDATED METALLOCERAMIC TYPE BY ELECTROLYTIC NICKELING |
US4936745A (en) * | 1988-12-16 | 1990-06-26 | United Technologies Corporation | Thin abradable ceramic air seal |
AU3323193A (en) * | 1991-12-24 | 1993-07-28 | Detroit Diesel Corporation | Thermal barrier coating and method of depositing the same on combustion chamber component surfaces |
GB9414858D0 (en) * | 1994-07-22 | 1994-09-14 | Baj Coatings Ltd | Protective coating |
GB9414859D0 (en) * | 1994-07-22 | 1994-09-14 | Baj Coatings Ltd | Protective coating |
US6422008B2 (en) | 1996-04-19 | 2002-07-23 | Engelhard Corporation | System for reduction of harmful exhaust emissions from diesel engines |
US5987882A (en) * | 1996-04-19 | 1999-11-23 | Engelhard Corporation | System for reduction of harmful exhaust emissions from diesel engines |
FR2787472B1 (en) | 1998-12-16 | 2001-03-09 | Onera (Off Nat Aerospatiale) | PROCESS FOR PRODUCING A METAL ALLOY POWDER OF THE MCRALY TYPE AND COATINGS OBTAINED THEREWITH |
FR2807073B1 (en) * | 2000-03-29 | 2002-06-21 | Onera (Off Nat Aerospatiale) | PROCESS FOR FORMING A SULFUR-FREE PROTECTIVE METAL COATING ON A METAL SUBSTRATE |
US6655369B2 (en) | 2001-08-01 | 2003-12-02 | Diesel Engine Transformations Llc | Catalytic combustion surfaces and method for creating catalytic combustion surfaces |
US6592948B1 (en) * | 2002-01-11 | 2003-07-15 | General Electric Company | Method for masking selected regions of a substrate |
US6998151B2 (en) * | 2002-05-10 | 2006-02-14 | General Electric Company | Method for applying a NiAl based coating by an electroplating technique |
EP1411210A1 (en) * | 2002-10-15 | 2004-04-21 | ALSTOM Technology Ltd | Method of depositing an oxidation and fatigue resistant MCrAIY-coating |
EP1426458B1 (en) * | 2002-12-06 | 2008-03-12 | ALSTOM Technology Ltd | Method of locally depositing a MCrAlY coating |
DE60231084D1 (en) * | 2002-12-06 | 2009-03-19 | Alstom Technology Ltd | Method for the selective deposition of an MCrAlY coating |
EP1491657B1 (en) * | 2003-06-26 | 2006-08-30 | ALSTOM Technology Ltd | Method of applying a coating system |
EP1491658A1 (en) * | 2003-06-26 | 2004-12-29 | ALSTOM Technology Ltd | Method of applying a coating system |
US20050025893A1 (en) * | 2003-07-31 | 2005-02-03 | Smith Clifford L. | Composite tool coating system |
US7604726B2 (en) * | 2004-01-07 | 2009-10-20 | Honeywell International Inc. | Platinum aluminide coating and method thereof |
US20080290138A1 (en) * | 2007-05-22 | 2008-11-27 | David Myron Lineman | Method for bonding refractory ceramic and metal |
EP2096194B1 (en) * | 2008-02-19 | 2016-06-01 | Parker-Hannifin Corporation | Protective coating for metallic seals |
JP4564545B2 (en) * | 2008-03-25 | 2010-10-20 | 株式会社東芝 | Coating method |
FR2954780B1 (en) * | 2009-12-29 | 2012-02-03 | Snecma | METHOD FOR THE ELECTROLYTIC DEPOSITION OF A METALLIC MATRIX COMPOSITE COATING CONTAINING PARTICLES FOR THE REPAIR OF A METAL BLADE |
US8367160B2 (en) | 2010-11-05 | 2013-02-05 | United Technologies Corporation | Coating method for reactive metal |
US8778164B2 (en) | 2010-12-16 | 2014-07-15 | Honeywell International Inc. | Methods for producing a high temperature oxidation resistant coating on superalloy substrates and the coated superalloy substrates thereby produced |
US9771661B2 (en) | 2012-02-06 | 2017-09-26 | Honeywell International Inc. | Methods for producing a high temperature oxidation resistant MCrAlX coating on superalloy substrates |
EP3111049A1 (en) | 2014-02-25 | 2017-01-04 | Siemens Aktiengesellschaft | Turbine abradable layer with airflow directing pixelated surface feature patterns |
US8939706B1 (en) | 2014-02-25 | 2015-01-27 | Siemens Energy, Inc. | Turbine abradable layer with progressive wear zone having a frangible or pixelated nib surface |
US9151175B2 (en) | 2014-02-25 | 2015-10-06 | Siemens Aktiengesellschaft | Turbine abradable layer with progressive wear zone multi level ridge arrays |
US9243511B2 (en) | 2014-02-25 | 2016-01-26 | Siemens Aktiengesellschaft | Turbine abradable layer with zig zag groove pattern |
US10087540B2 (en) | 2015-02-17 | 2018-10-02 | Honeywell International Inc. | Surface modifiers for ionic liquid aluminum electroplating solutions, processes for electroplating aluminum therefrom, and methods for producing an aluminum coating using the same |
WO2016133581A1 (en) | 2015-02-18 | 2016-08-25 | Siemens Aktiengesellschaft | Turbine shroud with abradable layer having composite non-inflected triple angle ridges and grooves |
WO2016133982A1 (en) | 2015-02-18 | 2016-08-25 | Siemens Aktiengesellschaft | Forming cooling passages in thermal barrier coated, combustion turbine superalloy components |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4305792A (en) * | 1977-12-21 | 1981-12-15 | Bristol Aerojet Limited | Processes for the electrodeposition of composite coatings |
JPS55112804A (en) * | 1979-02-26 | 1980-09-01 | Toshiba Corp | Manufacturing gas turbine blade |
JPS58167764A (en) * | 1982-03-26 | 1983-10-04 | Toyo Eng Corp | Method for coating heat resistant alloy substrate |
JPS5950752A (en) * | 1982-09-14 | 1984-03-23 | Aichi Emason Denki Kk | Manufacture of rotary electric machine core |
IL75304A (en) * | 1984-06-08 | 1989-03-31 | United Technologies Corp | Coated superalloy articles and method of strengthening same |
GB2167446B (en) * | 1984-10-05 | 1988-05-05 | Baj Ltd | Electrode deposited composite coating |
US4588607A (en) * | 1984-11-28 | 1986-05-13 | United Technologies Corporation | Method of applying continuously graded metallic-ceramic layer on metallic substrates |
EP0185603B1 (en) * | 1984-11-28 | 1989-11-08 | United Technologies Corporation | Improved durability metallic-ceramic turbine air seals |
-
1987
- 1987-03-24 GB GB878706951A patent/GB8706951D0/en active Pending
-
1988
- 1988-03-23 DE DE8888302546T patent/DE3872294T2/en not_active Expired - Lifetime
- 1988-03-23 EP EP88302546A patent/EP0288156B1/en not_active Expired
- 1988-03-23 ES ES198888302546T patent/ES2032552T3/en not_active Expired - Lifetime
- 1988-03-23 GB GB8806888A patent/GB2204881B/en not_active Expired - Fee Related
- 1988-03-23 CA CA000562171A patent/CA1324104C/en not_active Expired - Lifetime
- 1988-03-24 JP JP63070831A patent/JP2704878B2/en not_active Expired - Lifetime
- 1988-03-24 US US07/173,237 patent/US4810334A/en not_active Expired - Lifetime
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