JP2017052670A - Sealing agent, sealing agent coating solution, corrosion-resistant coating film, high-temperature member, and method for producing high-temperature member - Google Patents
Sealing agent, sealing agent coating solution, corrosion-resistant coating film, high-temperature member, and method for producing high-temperature member Download PDFInfo
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本発明は、耐食性被膜の気孔を埋めるための封孔剤と、これを用いて作製した耐食性被膜及び高温部材に関する。 The present invention relates to a sealing agent for filling pores of a corrosion-resistant film, a corrosion-resistant film produced using the same, and a high-temperature member.
火力発電では石炭や石油、ＬＮＧをボイラーで燃焼させ、その高温高圧のガスを使ってタービンを回転させたり、高温ガスの熱を使って発生させた蒸気でタービンを回転させたりすることで発電を行っている。このためガスタービンや伝熱管などの高温部材は、５００〜１０００℃の酸素や硫黄酸化物、硫化水素などの腐食性、酸化性の燃焼ガス雰囲気に晒される。その結果、いわゆる高温腐食による寿命低下が問題となる。 In thermal power generation, coal, oil, and LNG are burned in a boiler, and the turbine is rotated using the high-temperature and high-pressure gas, or the turbine is rotated by steam generated using the heat of the high-temperature gas. Is going. For this reason, high temperature members, such as a gas turbine and a heat exchanger tube, are exposed to corrosive and oxidizing combustion gas atmospheres, such as oxygen, sulfur oxide, and hydrogen sulfide of 500-1000 degreeC. As a result, there is a problem of a decrease in life due to so-called high temperature corrosion.
このような酸性ガスによる腐食が原因で高温部材の劣化が起こるため、高温部材の交換を頻繁に行う必要がある。高温部材の交換は発電コストを高めることになるから、より長期間劣化の起こらない高温部材が求められている。 Since the high temperature member deteriorates due to the corrosion caused by the acid gas, it is necessary to frequently replace the high temperature member. Since replacement of the high temperature member increases the power generation cost, a high temperature member that does not deteriorate for a longer period of time is required.
そこでこれらの高温部材の表面に耐食性被膜を形成して劣化を防止することが検討されている。耐食性被膜によって高温部材の寿命を延ばすには、如何にして気孔のない緻密な被膜を形成するかが重要となる。つまり耐食性被膜に気孔が存在すると、気孔を通して酸性ガスが高温部材の基材に到達してしまい、高温部材を腐食させてしまう。 Therefore, it has been studied to prevent deterioration by forming a corrosion-resistant film on the surface of these high-temperature members. In order to extend the life of the high-temperature member by the corrosion-resistant coating, it is important how to form a dense coating without pores. That is, if pores exist in the corrosion-resistant film, the acidic gas reaches the base material of the high temperature member through the pores, and the high temperature member is corroded.
例えば特許文献１には、下地層としてサーメットまたはセラミックスを溶射によって形成し、下地層表面に酸化物セラミックによる封孔処理を施し、さらにはガラス質被膜を形成した複合被膜が開示されている。特許文献１に記載の複合被膜は、貫通気孔が無く、腐食性ガスに対して優れた耐食性を示すだけでなく、基材の使用寿命が著しく向上されるとしている。封孔剤としては、耐熱性有機樹脂セラミックス懸濁液、加熱によってＣｒ２Ｏ３を生成するクロム酸、焼成することによって金属酸化物を生成する無機金属化合物の溶液およびコロイド液、金属アルコキシドアルコール溶液、金属塩化物の水溶液またはアルコール溶液、金属燐酸塩水溶液、金属水酸化物のコロイド液、金属酸化物超微粉を含むアルコールまたは水懸濁液あるいはこれらの２種以上の混合液が推奨されている。しかし、これらの封孔剤は固化後にもガスが発生し完全な封孔ができないという問題がある。また無機バインダーとして、Ｎａ２ＳｉＯ３、ＮａＰＯ３、ＮａＨＳｉＯ３の使用も提案されているが、これらはアルカリ金属を含む。特許文献２に記載のように、アルカリ金属は高温腐食の原因となるので、上記した無機バインダーを使用すると、これらが基材や被膜を腐食させてしまうおそれがある。 For example, Patent Document 1 discloses a composite coating in which cermet or ceramics is formed by thermal spraying as a base layer, a sealing process is performed on the surface of the base layer with an oxide ceramic, and a glassy coating is further formed. The composite coating described in Patent Document 1 has no through pores and exhibits not only excellent corrosion resistance against corrosive gas, but also the service life of the substrate is remarkably improved. Examples of sealing agents include heat-resistant organic resin ceramic suspensions, chromic acid that generates Cr 2 O 3 by heating, inorganic metal compound solutions and colloidal solutions that generate metal oxides by firing, metal alkoxide alcohol solutions Metal chloride aqueous solution or alcohol solution, metal phosphate aqueous solution, metal hydroxide colloid solution, alcohol or water suspension containing metal oxide ultrafine powder, or a mixture of two or more of these are recommended . However, these sealing agents have a problem that gas is generated even after solidification and complete sealing cannot be performed. Moreover, although the use of Na 2 SiO 3 , NaPO 3 , NaHSiO 3 as an inorganic binder has been proposed, these include alkali metals. As described in Patent Document 2, since alkali metals cause high-temperature corrosion, if the above-described inorganic binder is used, these may corrode a base material or a coating film.
本発明は上記事情を考慮してなされたものであり、耐食性被膜の気孔を長期に亘って封孔でき、しかも基材を腐食させることのない封孔剤を提供することを課題とする。 This invention is made | formed in view of the said situation, and makes it a subject to provide the sealing agent which can seal the pore of a corrosion-resistant film over a long period of time, and does not corrode a base material.
本発明の封孔剤は、耐食性被膜の気孔を封孔するための封孔剤であって、軟化点が９００℃以下、且つ組成に占めるアルカリ金属酸化物の割合が２０質量％以下である非晶質ガラスからなることを特徴とする。「非晶質ガラス」とは、軟化点＋４０℃、３０分の条件で熱処理したときに、結晶が析出しない性質を有するガラスを意味する。「アルカリ金属酸化物」とは、Ｌｉ２Ｏ、Ｎａ２Ｏ及びＫ２Ｏの一種以上を指す。 The sealing agent of the present invention is a sealing agent for sealing pores of a corrosion-resistant film, and has a softening point of 900 ° C. or less and a proportion of alkali metal oxides in the composition of 20% by mass or less. It consists of crystalline glass. “Amorphous glass” means glass having a property that crystals do not precipitate when heat-treated at a softening point of + 40 ° C. for 30 minutes. “Alkali metal oxide” refers to one or more of Li 2 O, Na 2 O, and K 2 O.
上記構成を有する封孔剤は、低軟化点のガラスからなるため、高温部材が高温に晒されると封孔剤が溶融状態となって流動して気孔内を満たすことから、耐食性被膜の気孔を封孔することができる。またアルカリ金属成分が少ないため、基材を腐食させることがない。 Since the sealing agent having the above-described structure is made of glass having a low softening point, when the high temperature member is exposed to a high temperature, the sealing agent enters a molten state and flows to fill the pores. Can be sealed. Moreover, since there are few alkali metal components, a base material is not corroded.
ところで火力発電設備が、例えば修理等によって操業を一旦中止し、高温部材が冷却された場合、高温部材等との膨張差によって封孔剤に割れが生じることがある。このような事態が生じた場合であっても、本発明の封孔剤は非晶質ガラスからなるため、設備が再稼働して高温部材が高温に晒されるようになると、封孔剤が再溶融する。その結果、封孔剤の割れが消失するため、再び封孔状態に戻すことができる。 By the way, when the thermal power generation facility temporarily stops operation, for example, by repair or the like and the high temperature member is cooled, the sealing agent may be cracked due to a difference in expansion from the high temperature member or the like. Even when such a situation occurs, the sealing agent of the present invention is made of amorphous glass. Therefore, when the equipment is restarted and the high temperature member is exposed to a high temperature, the sealing agent is restarted. Melt. As a result, since the crack of the sealing agent disappears, it can be returned to the sealing state again.
本発明においては、非晶質ガラスが、ガラス組成として、質量百分率でＢ２Ｏ３ １０〜５０％、ＺｎＯ ０〜７０％、ＭｇＯ＋ＣａＯ＋ＳｒＯ＋ＢａＯ ０〜８０％、Ｌｉ２Ｏ＋Ｎａ２Ｏ＋Ｋ２Ｏ ０〜２０％、ＳｉＯ２ ０〜５０％、Ａｌ２Ｏ３ ０〜３０％含有することが好ましい。ここで「ＭｇＯ＋ＣａＯ＋ＳｒＯ＋ＢａＯ」は、ＭｇＯ、ＣａＯ、ＳｒＯ及びＢａＯの合量を意味する。「Ｌｉ２Ｏ＋Ｎａ２Ｏ＋Ｋ２Ｏ」はＬｉ２Ｏ、Ｎａ２Ｏ及びＫ２Ｏの合量を意味する。 In the present invention, the amorphous glass has a glass composition including, B 2 O 3 10~50% in percent by mass, ZnO 0~70%, MgO + CaO + SrO + BaO 0~80%, Li 2 O + Na 2 O + K 2 O 0~20% , SiO 2 0-50%, Al 2 O 3 0-30% are preferable. Here, “MgO + CaO + SrO + BaO” means the total amount of MgO, CaO, SrO and BaO. “Li 2 O + Na 2 O + K 2 O” means the total amount of Li 2 O, Na 2 O and K 2 O.
上記構成を採用すれば、非晶質で、且つ低軟化点の封孔剤を作製することが容易になる。 If the above configuration is adopted, it becomes easy to produce a sealing agent that is amorphous and has a low softening point.
本発明においては、非晶質ガラスが、Ｂ２Ｏ３−ＺｎＯ系ガラスであることが好ましい。ここで「Ｂ２Ｏ３−ＺｎＯ系ガラス」とは、ガラス組成としてＢ２Ｏ３を１０質量％以上、且つＺｎＯを１質量％以上含有するガラスを指す。 In the present invention, the amorphous glass is preferably B 2 O 3 —ZnO-based glass. Here, “B 2 O 3 —ZnO-based glass” refers to glass containing 10% by mass or more of B 2 O 3 and 1% by mass or more of ZnO as a glass composition.
本発明の封孔剤塗布液は、上記の封孔剤を含むことを特徴とする。 The sealing agent coating liquid of the present invention contains the above-mentioned sealing agent.
上記構成を採用すれば、刷毛塗り等の簡便な方法によって、封孔剤を耐食性被膜上に塗布することが容易になる。 If the said structure is employ | adopted, it will become easy to apply | coat a sealing agent on a corrosion-resistant film by simple methods, such as brush coating.
本発明の耐食性被膜は、ＺｒＯ２、Ａｌ２Ｏ３及びＳｉＯ２から選ばれる１種以上を５０質量％以上含む耐食性被膜であって、上記の封孔剤からなる粉末が表面に付着していることを特徴とする。「表面に付着している」とは、封孔剤粉末が耐食性被膜に化学的、物理的に結合している状態に加え、封孔剤粉末が幾何的に耐食性被膜に引っかかり脱落しない状態を含む。 The corrosion-resistant film of the present invention is a corrosion-resistant film containing 50% by mass or more of at least one selected from ZrO 2 , Al 2 O 3 and SiO 2, and the powder composed of the above-mentioned sealing agent is attached to the surface. It is characterized by that. “Adhering to the surface” includes not only the state where the sealant powder is chemically and physically bonded to the corrosion-resistant coating, but also the state where the sealant powder is geometrically caught by the corrosion-resistant coating and does not fall off. .
上記構成を有する耐食性被膜を採用した高温部材は、使用時の高温雰囲気を利用して耐食性被膜の気孔を封孔することが可能であるため、事前の焼成工程を省略することができる。 The high-temperature member employing the corrosion-resistant coating having the above-described configuration can seal the pores of the corrosion-resistant coating using a high-temperature atmosphere at the time of use, so that the preliminary firing step can be omitted.
また本発明の耐食性被膜は、ＺｒＯ２、Ａｌ２Ｏ３及びＳｉＯ２から選ばれる１種以上を５０質量％以上含む耐食性被膜であって、表面に存在する気孔の一部または全体が上記の封孔剤で満たされていることを特徴とする。 The corrosion-resistant film of the present invention is a corrosion-resistant film containing 50% by mass or more of one or more selected from ZrO 2 , Al 2 O 3 and SiO 2, and part or all of the pores existing on the surface are sealed as described above. It is filled with a pore agent.
上記構成を有する耐食性被膜を採用した高温部材は、封孔剤が耐食性被膜の気孔内に固定されているため、移送中や使用箇所への設置の際に、封孔剤層が脱落したり、破損したりする事態を効果的に回避できる。 The high-temperature member employing the corrosion-resistant coating having the above-mentioned configuration is because the sealing agent is fixed in the pores of the corrosion-resistant coating, so that the sealing agent layer may fall off during installation during installation or use, The situation where it breaks can be avoided effectively.
本発明の高温部材は、基材の表面に、上記の耐食性被膜が形成されていることを特徴とする。 The high temperature member of the present invention is characterized in that the above-mentioned corrosion-resistant film is formed on the surface of a base material.
本発明の高温部材の製造方法は、基材上にＺｒＯ２、Ａｌ２Ｏ３及びＳｉＯ２から選ばれる１種以上を５０質量％以上含む耐食性被膜を形成する工程と、耐食性被膜上に上記の封孔剤塗布液を塗布することを特徴とする。なお塗布後に封孔剤塗布液を乾燥させることが好ましい。 The method for producing a high-temperature member of the present invention includes a step of forming a corrosion-resistant film containing 50% by mass or more of at least one selected from ZrO 2 , Al 2 O 3 and SiO 2 on a base material, A sealing agent coating solution is applied. In addition, it is preferable to dry a sealing agent coating liquid after application | coating.
本発明においては、封孔剤塗布液の塗布後（或いは乾燥後）に焼成する工程を有することが好ましい。 In this invention, it is preferable to have the process baked after application | coating (or after drying) of sealing agent coating liquid.
以下、本発明の実施形態について説明する。 Hereinafter, embodiments of the present invention will be described.
本発明の封孔剤は、耐食性被膜に存在する気孔を封孔するものである。本発明の封孔剤を適用できる耐食性被膜は特に制限はなく、例えばＺｒＯ２、Ａｌ２Ｏ３及びＳｉＯ２から選ばれる１種以上を５０質量％以上含む耐食性被膜の封孔剤として使用できる。 The sealing agent of this invention seals the pore which exists in a corrosion-resistant film. The corrosion resistant coating to which the sealing agent of the present invention can be applied is not particularly limited, and can be used as a sealing agent for a corrosion resistant coating containing 50% by mass or more of at least one selected from ZrO 2 , Al 2 O 3 and SiO 2 .
封孔剤を構成する非晶質ガラスは、軟化点が９００℃以下、８５０℃以下、特に８００℃以下であることが好ましい。軟化点が高すぎると、使用温度域においてガラスが溶融状態となりにくくなる。なお軟化点は低いほど有利であるが、低すぎると使用温度域でのガラスの粘性が低くなり過ぎて、耐食性被膜の表面から流失してしまうことがある。このような場合、軟化点は４００℃以上、特に５００℃以上とすることが好ましい。 The amorphous glass constituting the sealant preferably has a softening point of 900 ° C. or lower, 850 ° C. or lower, particularly 800 ° C. or lower. If the softening point is too high, the glass becomes difficult to be in a molten state in the operating temperature range. The lower the softening point, the more advantageous. However, if the softening point is too low, the viscosity of the glass in the operating temperature range becomes too low and the glass may be washed away from the surface of the corrosion-resistant coating. In such a case, the softening point is preferably 400 ° C. or higher, particularly 500 ° C. or higher.
封孔剤を構成するガラスは、ガラス組成中に占めるアルカリ金属酸化物の割合が２０質量％以下である。アルカリ金属酸化物は、ガラスの粘度を下げて低軟化点を達成するための成分であるが、高温腐食の原因となってしまう。よってガラス組成中に含まれるアルカリ金属酸化物の総量（Ｌｉ２Ｏ＋Ｎａ２Ｏ＋Ｋ２Ｏ）は０〜２０％であり、０．１〜１８％、１〜１５％、特に５〜１２％であることが好ましい。なおＬｉ２Ｏの含有量は０〜２０％、０〜１５％、０〜１０％、特に０．１〜５％であることが好ましく、Ｎａ２Ｏの含有量は０〜２０％、０．１〜１５％、１〜１３％、特に１．５〜１２％であることが好ましい。Ｋ２Ｏの含有量は０〜２０％、１〜１５％、特に５〜１３％であることが好ましい。 In the glass constituting the sealing agent, the proportion of the alkali metal oxide in the glass composition is 20% by mass or less. Alkali metal oxide is a component for lowering the viscosity of glass to achieve a low softening point, but it causes high temperature corrosion. Therefore, the total amount of the alkali metal oxide (Li 2 O + Na 2 O + K 2 O) contained in the glass composition is 0 to 20%, 0.1 to 18%, 1 to 15%, particularly 5 to 12%. Is preferred. The Li 2 O content is preferably 0 to 20%, 0 to 15%, 0 to 10%, particularly preferably 0.1 to 5%, and the Na 2 O content is 0 to 20%, 0. It is preferably 1 to 15%, 1 to 13%, particularly preferably 1.5 to 12%. The content of K 2 O is preferably 0 to 20%, 1 to 15%, particularly preferably 5 to 13%.
封孔剤を構成する非晶質ガラスは、例えばガラス組成として、質量百分率でＢ２Ｏ３ １０〜５０％、ＺｎＯ １〜７０％、ＭｇＯ＋ＣａＯ＋ＳｒＯ＋ＢａＯ ０〜８０％、Ｌｉ２Ｏ＋Ｎａ２Ｏ＋Ｋ２Ｏ ０〜２０％、ＳｉＯ２ ０〜５０％、Ａｌ２Ｏ３ ０〜３０％含有するものを使用することができる。ガラス組成を上記のように限定した理由を以下に説明する。なお以下の記載において「％」は質量％を意味する。 The amorphous glass constituting the sealant is, for example, in terms of glass composition, B 2 O 3 10-50%, ZnO 1-70%, MgO + CaO + SrO + BaO 0-80%, Li 2 O + Na 2 O + K 2 O 0 20%, SiO 2 0~50%, it may be used those containing Al 2 O 3 0~30%. The reason for limiting the glass composition as described above will be described below. In the following description, “%” means mass%.
Ｂ２Ｏ３は、ガラスの網目形成酸化物である。Ｂ２Ｏ３の含有量が多すぎると耐水性が低くなり通常湿度での取扱いが難しくなる。Ｂ２Ｏ３の含有量が少なすぎるとガラスが不安定になって失透しやすくなる。Ｂ２Ｏ３の含有量は１０〜５０％、１０％超〜５０％、１５〜４０％、特に２０〜３５％であることが好ましい。 B 2 O 3 is a glass network-forming oxide. B handling in the 2 O 3 of the content is too great water resistance is lowered normal humidity is difficult. B 2 When the content of O 3 is too small glass tends to be devitrified and becomes unstable. The content of B 2 O 3 is preferably 10 to 50%, more than 10% to 50%, 15 to 40%, particularly preferably 20 to 35%.
ＺｎＯは、中間酸化物としてガラス形成に寄与する成分でもある。ＺｎＯの含有量が多すぎると失透しやすくなり、含有量が少なすぎると溶融温度が高くなって溶融し難くなったり、ガラスが不安定になったりする。ＺｎＯの含有量は０〜７０％、１〜７０％、５〜６０％、１０〜５０％、特に１５〜４５％であることが好ましい。 ZnO is also a component contributing to glass formation as an intermediate oxide. If the content of ZnO is too large, devitrification is likely to occur, and if the content is too small, the melting temperature becomes high and it becomes difficult to melt, or the glass becomes unstable. The content of ZnO is preferably 0 to 70%, 1 to 70%, 5 to 60%, 10 to 50%, particularly preferably 15 to 45%.
ＭｇＯ＋ＣａＯ＋ＳｒＯ＋ＢａＯは、０〜８０％、特に５〜２５％であることが好ましい。ＭｇＯ＋ＣａＯ＋ＳｒＯ＋ＢａＯが多すぎると失透しやすくなる。 MgO + CaO + SrO + BaO is preferably 0 to 80%, particularly preferably 5 to 25%. When there is too much MgO + CaO + SrO + BaO, it will become easy to devitrify.
ＭｇＯは、ガラスの溶融温度を低下させ、また熱膨張係数を調整する成分である。ＭｇＯの含有量が多すぎると失透しやすくなり、含有量が少なすぎると溶融温度が高くなって溶融し難くなる。ＭｇＯの含有量は０〜４０％、１〜２５％、特に２〜１０％であることが好ましい。 MgO is a component that lowers the melting temperature of the glass and adjusts the thermal expansion coefficient. When there is too much content of MgO, it will become easy to devitrify, and when there is too little content, a melting temperature will become high and it will become difficult to fuse | melt. The content of MgO is preferably 0 to 40%, 1 to 25%, particularly preferably 2 to 10%.
ＣａＯは、ガラスの溶融温度を低下させ、また熱膨張係数を調整する成分である。ＣａＯの含有量が多すぎると失透しやすくなり、含有量が少なすぎると溶融温度が高くなって溶融し難くなる。ＣａＯの含有量は０〜４０％、１〜３０％、特に２〜２０％であることが好ましい。 CaO is a component that lowers the melting temperature of the glass and adjusts the thermal expansion coefficient. When there is too much content of CaO, it will become easy to devitrify, and when there is too little content, a melting temperature will become high and it will become difficult to fuse | melt. The CaO content is preferably 0 to 40%, 1 to 30%, particularly preferably 2 to 20%.
ＳｒＯは、ガラスの溶融温度を低下させ、また熱膨張係数を調整する成分である。ＳｒＯの含有量が多すぎると失透しやすくなり、含有量が少なすぎると溶融温度が高くなって溶融し難くなる。ＳｒＯの含有量は０〜４０％、１〜３０％、特に２〜２０％であることが好ましい。 SrO is a component that lowers the melting temperature of the glass and adjusts the thermal expansion coefficient. When the content of SrO is too large, devitrification is likely to occur, and when the content is too small, the melting temperature becomes high and it becomes difficult to melt. The SrO content is preferably 0 to 40%, 1 to 30%, particularly preferably 2 to 20%.
ＢａＯは、ガラスの溶融温度を低下させ、また熱膨張係数を調整する成分である。ＢａＯの含有量が多すぎると失透しやすくなり、含有量が少なすぎると溶融温度が高くなって溶融し難くなる。ＢａＯの含有量は０〜５０％、１〜４０％、２〜３０％、特に５〜２５％であることが好ましい。 BaO is a component that lowers the melting temperature of the glass and adjusts the thermal expansion coefficient. When there is too much content of BaO, it will become easy to devitrify, and when there is too little content, a melting temperature will become high and it will become difficult to fuse | melt. The BaO content is preferably 0 to 50%, 1 to 40%, 2 to 30%, and particularly preferably 5 to 25%.
ＭｇＯ＋ＣａＯ＋ＳｒＯ＋ＢａＯ＋ＺｎＯは１０〜８０％、２０〜７０％、特に２５〜５０％であることが好ましい。なお「ＭｇＯ＋ＣａＯ＋ＳｒＯ＋ＢａＯ＋ＺｎＯ」はＭｇＯ、ＣａＯ、ＳｒＯ、ＢａＯ及びＺｎＯの含有量の合量を意味する。 MgO + CaO + SrO + BaO + ZnO is preferably 10 to 80%, 20 to 70%, particularly preferably 25 to 50%. “MgO + CaO + SrO + BaO + ZnO” means the total content of MgO, CaO, SrO, BaO and ZnO.
Ｌｉ２Ｏ＋Ｎａ２Ｏ＋Ｋ２Ｏについては既述の通りであり、ここでは説明を省略する。 Li 2 O + Na 2 O + K 2 O is as described above, and a description thereof is omitted here.
ＳｉＯ２は、ガラスの網目形成酸化物であり、ガラス形成に寄与すると同時に耐水性を上げる成分である。ＳｉＯ２の含有量が多すぎると失透しやすくなり、含有量が少なすぎると耐水性が低くなり、またガラスが不安定になる。ＳｉＯ２の含有量は０〜５０％、３〜４５％、特に５〜３０％であることが好ましい。 SiO 2 is a network-forming oxide of glass, and is a component that contributes to glass formation and simultaneously increases water resistance. If the content of SiO 2 is too large, devitrification tends to occur, and if the content is too small, the water resistance becomes low and the glass becomes unstable. The content of SiO 2 is preferably 0 to 50%, 3 to 45%, particularly 5 to 30%.
Ａｌ２Ｏ３は、耐水性を上げ、ガラスの粘度を上げる成分である。Ａｌ２Ｏ３の含有量が多すぎると失透しやすくなり、含有量が少なすぎると耐水性が低くなって通常湿度での取扱いが難しくなる。Ａｌ２Ｏ３の含有量は０〜３０％、２〜２０％、特に４〜１５％であることが好ましい。 Al 2 O 3 is a component that increases water resistance and increases the viscosity of the glass. When the content of Al 2 O 3 is too large, devitrification tends to occur, and when the content is too small, the water resistance becomes low and handling at normal humidity becomes difficult. The content of Al 2 O 3 is preferably 0 to 30%, 2 to 20%, particularly 4 to 15%.
上記の成分以外にも、所望の特性を損なわない範囲でＰ２Ｏ５、ＴｉＯ２、ＭｎＯ２、Ｆｅ２Ｏ３、ＣｏＯ、ＮｉＯ、ＣｕＯ、Ｙ２Ｏ３、ＺｒＯ２、ＳｎＯ２、Ｌａ２Ｏ３、ＣｅＯ２、Ｂｉ２Ｏ３等をそれぞれ１０％まで含んでも良い。 In addition to the above components, P 2 O 5 , TiO 2 , MnO 2 , Fe 2 O 3 , CoO, NiO, CuO, Y 2 O 3 , ZrO 2 , SnO 2 , and La 2 are within a range that does not impair the desired characteristics. O 3 , CeO 2 , Bi 2 O 3 and the like may be included up to 10% each.
封孔剤を構成する非晶質ガラスは、Ｂ２Ｏ３−ＺｎＯ系の非晶質ガラスからなることが好ましい。この系のガラスは軟化点が低く、高温部材の使用温度域で溶融状態となりやすい性質を有する。また非晶質であることから、溶融状態となった後に冷却されて固化しても、再度の加熱で再び溶融状態に戻るため、発電設備の稼働、停止が繰り返された場合であっても、設備の稼働時には常に溶融状態を維持できる。 The amorphous glass constituting the sealing agent is preferably made of B 2 O 3 —ZnO-based amorphous glass. This type of glass has a low softening point and has a property of being easily melted in the operating temperature range of the high temperature member. Also, since it is amorphous, even if it is cooled and solidified after becoming a molten state, it returns to the molten state again by heating, so even if the operation and stop of the power generation equipment are repeated, When the equipment is in operation, the molten state can always be maintained.
封孔剤を構成する非晶質ガラスは、３０〜３８０℃における熱膨張係数が３０〜１２０×１０−７／Ｋ、特に５０〜９０×１０−７／Ｋであることが好ましい。熱膨張係数が高すぎたり、低すぎたりすると、基材との熱膨張差によって生じる亀裂が大きくなり、発電設備の冷却過程で耐食性被膜表面から脱落してしまう可能性がある。 The amorphous glass constituting the sealant preferably has a thermal expansion coefficient at 30 to 380 ° C. of 30 to 120 × 10 −7 / K, particularly 50 to 90 × 10 −7 / K. If the thermal expansion coefficient is too high or too low, cracks caused by the difference in thermal expansion from the base material become large, and there is a possibility that the surface of the corrosion-resistant coating will fall off during the cooling process of the power generation equipment.
封孔剤を構成する非晶質ガラスは、平均粒径が１０ｎｍ〜５００μｍ、特に１〜１００μｍのガラス粉末であることが好ましい。ここで「平均粒径」とは、レーザー回折散乱法によって任意の粉末の粒径を測定した際、粒子の個数基準で算出されるＤ５０で定義されるものである。 The amorphous glass constituting the sealant is preferably a glass powder having an average particle size of 10 nm to 500 μm, particularly 1 to 100 μm. Here, the “average particle size” is defined by D50 calculated on the basis of the number of particles when the particle size of an arbitrary powder is measured by the laser diffraction scattering method.
本発明の封孔剤塗布液は、封孔剤を各種樹脂や塗料、有機溶媒、水などの無機溶媒と混ぜてペースト化又はスラリー化したものを指す。ペースト化又はスラリー化することにより、耐食性被膜上に均一に塗布し易くなる。また樹脂や塗料には、封孔剤が軟化して耐食性被膜から脱落しなくなるまでの間、封孔剤を被膜上に固定させる働きがある。このような樹脂や塗料として、例えば不飽和ポリエステル樹脂、エポキシ樹脂、シリコーン樹脂、ポリチタノカルボキシルシラン等を使用することができる。これらの中でも、耐熱性が高く、封孔剤が溶融状態（融液）になる温度で還元作用が小さいシリコーン樹脂を採用することが最も好ましい。 The sealant coating solution of the present invention refers to a paste or slurry obtained by mixing a sealant with various resins, paints, organic solvents, water and other inorganic solvents. By making it into a paste or slurry, it becomes easy to apply uniformly on the corrosion-resistant coating. Also, the resin or paint has a function of fixing the sealing agent on the coating until the sealing agent softens and does not fall off from the corrosion-resistant coating. As such a resin or paint, for example, an unsaturated polyester resin, an epoxy resin, a silicone resin, or polytitanocarboxylsilane can be used. Among these, it is most preferable to employ a silicone resin that has high heat resistance and a small reducing action at a temperature at which the sealing agent becomes a molten state (melt).
本発明の耐食性被膜は、ＺｒＯ２、Ａｌ２Ｏ３及びＳｉＯ２から選ばれる１種以上を５０質量％以上含む耐食性被膜である。この種の耐食性被膜は、例えば５００〜１０００℃の酸素や硫黄酸化物、硫化水素などの腐食性、酸化性の燃焼ガス雰囲気に対して耐食性を有し得るものである。 The corrosion-resistant film of the present invention is a corrosion-resistant film containing 50% by mass or more of one or more selected from ZrO 2 , Al 2 O 3 and SiO 2 . This type of corrosion-resistant coating can have corrosion resistance against corrosive and oxidizing combustion gas atmospheres of oxygen, sulfur oxides, hydrogen sulfide and the like at 500 to 1000 ° C., for example.
耐食性被膜の例として、安定化ＺｒＯ２を主たる構成成分とする耐食性被膜（以下、安定化ＺｒＯ２系耐食性被膜という）が挙げられる。安定化ＺｒＯ２は、ＺｒＯ２を主成分とし、Ｙ２Ｏ３、ＭｇＯ、ＣａＯ、ＳｉＯ２、ＣｅＯ２、Ｙｂ２Ｏ３、Ｄｙ２Ｏ３、ＨｆＯ２等から選ばれた１種類以上の安定化剤を添加したものである。具体的には、ＺｒＯ２の含有量が８５質量％以上、好ましくは８５〜９５質量％、安定化剤の含有量が１５質量％以下、好ましくは５〜１５質量％であるものを意味する。ＺｒＯ２の含有量が８５質量％以上であれば、被膜の耐食性が確保できるとともに、プラズマ溶射後の冷却過程において１０００℃付近で発生するＺｒＯ２の正方晶や立方晶から単斜晶への相転移も抑制することができる。なおＺｒＯ２の含有量が８５質量％よりも少ないと、被膜の耐食性が低下してしまう。 Examples of the corrosion resistant coating include a corrosion resistant coating having stabilized ZrO 2 as a main constituent (hereinafter referred to as a stabilized ZrO 2 -based corrosion resistant coating). Stabilized ZrO 2 is mainly composed of ZrO 2 , and one or more kinds of stable selected from Y 2 O 3 , MgO, CaO, SiO 2 , CeO 2 , Yb 2 O 3 , Dy 2 O 3 , HfO 2 and the like. An agent is added. Specifically, the ZrO 2 content is 85% by mass or more, preferably 85 to 95% by mass, and the stabilizer content is 15% by mass or less, preferably 5 to 15% by mass. If the ZrO 2 content is 85% by mass or more, the corrosion resistance of the coating can be ensured, and the phase from the tetragonal or cubic to monoclinic phase of ZrO 2 generated near 1000 ° C. in the cooling process after plasma spraying. Metastasis can also be suppressed. Incidentally the content of ZrO 2 is less than 85 wt%, the corrosion resistance of the coating is reduced.
耐食性被膜の気孔率は５％以下、特に４％以下であることが好ましい。耐食性被膜を緻密にすることによって、酸性ガスが被膜を透過することによって生じる基材の腐食を一層防止することが可能になる。耐食性被膜の気孔率が高すぎると、封孔剤によって気孔を完全に封孔することが難しくなり、酸性ガスの透過抑制が困難になる。ここで「気孔率が５％以下」とは、耐食性被膜の断面を走査型電子顕微鏡により倍率１０００倍で観察した際に、観察画面の面積に対する表面の割れや空隙の総面積の割合が５％以下であることを意味する。 The porosity of the corrosion-resistant film is preferably 5% or less, particularly 4% or less. By densifying the corrosion-resistant film, it becomes possible to further prevent the corrosion of the base material caused by the acidic gas permeating the film. When the porosity of the corrosion-resistant coating is too high, it becomes difficult to completely seal the pores with the sealing agent, and it becomes difficult to suppress permeation of acid gas. Here, “porosity is 5% or less” means that when the cross section of the corrosion-resistant coating is observed with a scanning electron microscope at a magnification of 1000 times, the ratio of the total area of cracks and voids to the surface of the observation screen is 5%. It means the following.
耐食性被膜の膜厚は１０〜１０００μｍ、１０〜５００μｍ、５０〜４００μｍ、特に７０〜３００μｍであることが好ましい。耐食性被膜の膜厚が小さすぎると、酸性ガスの透過抑制が困難になり易い。一方、耐食性被膜の膜厚が大きすぎると、熱サイクルによって発生する熱応力が大きくなり、耐食性被膜が剥離しやすくなる。なお耐食性被膜の気孔率は、溶射粉末（安定化ＺｒＯ２粉末や無機ガラス粉末）の粒径を変えることによって調整することができる。 The thickness of the corrosion-resistant coating is preferably 10 to 1000 μm, 10 to 500 μm, 50 to 400 μm, and particularly preferably 70 to 300 μm. If the thickness of the corrosion-resistant film is too small, it is difficult to suppress permeation of acidic gas. On the other hand, when the film thickness of the corrosion-resistant film is too large, the thermal stress generated by the thermal cycle increases, and the corrosion-resistant film easily peels off. The porosity of the corrosion-resistant coating can be adjusted by changing the particle size of the sprayed powder (stabilized ZrO 2 powder or inorganic glass powder).
本発明の高温部材は、上述の耐食性被膜が形成されていることが好ましい。尚、高温部材本体（基材）の材料としては、Ｆｅ、Ｎｉ、Ｃｏ、Ｃｒの少なくとも１つを主成分とする金属材料が好ましい。また耐食性被膜は基材上に直接形成されることが好ましいが、密着性等を向上させる目的で、基材と耐食性被膜の間に１層又は２層以上の下地層を設けても差し支えない。 The high temperature member of the present invention preferably has the above-mentioned corrosion-resistant film formed thereon. In addition, as a material of a high temperature member main body (base material), the metal material which has at least one of Fe, Ni, Co, and Cr as a main component is preferable. The corrosion-resistant coating is preferably formed directly on the substrate, but for the purpose of improving adhesion and the like, one or more underlayers may be provided between the substrate and the corrosion-resistant coating.
例えばＳＵＳからなる基材上に、上記した安定化ＺｒＯ２系耐食性被膜を形成する場合、下地層として、例えばＭ−Ｃｒ−Ａｌ−Ｙ系合金（Ｍ＝Ｎｉ、Ｃｏ、Ｆｅ）からなる層を設けることが好ましい。Ｍ−Ｃｒ−Ａｌ−Ｙ系合金は、耐高温酸化性や耐高温腐食性に優れた性質を有するＮｉあるいはＣｏを主成分とし、Ｃｒ、Ａｌ及びＹを添加した合金である。この種の合金は、ＳＵＳ及び安定化ＺｒＯ２系耐食性被膜の双方に密着し易いという特徴がある。 For example, when the above-described stabilized ZrO 2 -based corrosion-resistant film is formed on a substrate made of SUS, a layer made of, for example, an M—Cr—Al—Y alloy (M = Ni, Co, Fe) is used as the underlayer. It is preferable to provide it. The M-Cr-Al-Y alloy is an alloy mainly composed of Ni or Co having excellent high-temperature oxidation resistance and high-temperature corrosion resistance, and added with Cr, Al, and Y. This type of alloy is characterized in that it easily adheres to both SUS and the stabilized ZrO 2 -based corrosion resistant coating.
下地層の気孔率は１％以下であることが好ましい。酸性ガスの透過抑制の観点から、下地層の気孔率は低いほど有利になる。 The porosity of the underlayer is preferably 1% or less. From the viewpoint of suppressing permeation of acid gas, the lower the porosity of the underlayer, the more advantageous.
下地層の膜厚は１０〜５００μｍ、特に５０〜４００μｍ、さらには７０〜３５０μｍであることが好ましい。酸性ガスの透過抑制の観点から、下地層の膜厚は厚いほど有利になる。また下地層は、一般に基材と耐食性被膜の界面に生じる熱膨張特性の相違に起因した熱応力を緩和する効果を有するが、下地層の膜厚が小さすぎると熱応力の緩和効果を得難くなる。一方、下地層の膜厚が大きすぎると、発電設備内部の熱サイクル等によって発生する熱応力が大きくなり、下地層が剥離し易くなる。なお下地層の気孔率は、溶射するＭ−Ｃｒ−Ａｌ−Ｙ系合金粉末等の粒径を変えることによって調整することができる。 The film thickness of the underlayer is preferably 10 to 500 μm, particularly 50 to 400 μm, and more preferably 70 to 350 μm. From the viewpoint of suppressing permeation of acid gas, the thicker the base layer, the more advantageous. In addition, the underlayer generally has an effect of relieving thermal stress due to the difference in thermal expansion characteristics generated at the interface between the base material and the corrosion-resistant film, but it is difficult to obtain a thermal stress mitigating effect if the underlayer is too thin. Become. On the other hand, if the film thickness of the underlayer is too large, thermal stress generated by a heat cycle or the like inside the power generation facility increases, and the underlayer is easily peeled off. The porosity of the underlayer can be adjusted by changing the particle diameter of the M-Cr-Al-Y alloy powder to be sprayed.
高温部材は、蒸気や空気等の流体を介して運動エネルギーや熱エネルギーを回収して発電を行う火力発電のタービンや伝熱管であることが好ましい。ただしこれらに限定されるものでない。例えば、各種エンジン等などにも好適に適用できる。 The high-temperature member is preferably a thermal power generation turbine or heat transfer tube that generates power by collecting kinetic energy or thermal energy via a fluid such as steam or air. However, it is not limited to these. For example, it can be suitably applied to various engines.
次に本発明の封孔剤を利用した高温部材の製造方法を、ＳＵＳからなる基材上に、Ｍ−Ｃｒ−Ａｌ−Ｙ系合金からなる下地層を介して、安定化ＺｒＯ２系耐食性被膜を形成する場合を例にとって説明する。なお以下の説明において、基材として金属管を用いれば、耐食性被膜付き伝熱管を作製することができる。なお本発明の製造方法は以下の説明に制限されるものではない。当然ながら下地層の形成が必須要件でないことは言うまでもない。 Next, the manufacturing method of the high temperature member using the sealing agent of the present invention is a stabilized ZrO 2 -based corrosion-resistant coating film on a base material made of SUS with an underlayer made of an M-Cr-Al-Y alloy. An example of forming the case will be described. In the following description, if a metal tube is used as the substrate, a heat transfer tube with a corrosion-resistant coating can be produced. The production method of the present invention is not limited to the following description. Of course, it goes without saying that the formation of the underlayer is not an essential requirement.
まずＳＵＳからなる基材上に、Ｍ−Ｃｒ−Ａｌ−Ｙ系合金からなる下地層を形成する。 First, an underlayer made of an M—Cr—Al—Y alloy is formed on a base material made of SUS.
下地層の形成は、特に制限されるものではないが、高速フレーム溶射（ＨＶＯＦ）のようなガス溶射によって形成されることが好ましい。高速フレーム溶射を用いることで、基材であるＳＵＳとの密着性が良く、気孔率も低い下地層を得やすくなる。またこの際に用いる溶射粉末には、Ｍ−Ｃｒ−Ａｌ−Ｙ系合金からなる粉末を使用することが好ましい。Ｍ−Ｃｒ−Ａｌ−Ｙ系合金については既述の通りであり、ここではその説明を省略する。また溶射粉末の平均粒径は１０〜７５μｍ、１０〜５３μｍ、特に１０〜４５μｍであることが好ましい。溶射粉末の粒径が大きいと、ガス溶射によって形成される下地層の気孔率が高くなる。また溶射粉末の粒径が小さいと溶射粉末をガスあるいはプラズマに供給する、ポートと呼ばれる噴出口の詰まりが発生しやすくなり、任意の膜厚の溶射被膜の形成に時間がかかり、結果的に溶射コストが高くなり易い。 The formation of the underlayer is not particularly limited, but is preferably formed by gas spraying such as high-speed flame spraying (HVOF). By using high-speed flame spraying, it becomes easy to obtain a base layer having good adhesion to SUS as a base material and low porosity. Moreover, it is preferable to use the powder which consists of a M-Cr-Al-Y type alloy for the thermal spraying powder used in this case. The M-Cr-Al-Y alloy is as described above, and the description thereof is omitted here. The average particle size of the sprayed powder is preferably 10 to 75 μm, 10 to 53 μm, and particularly preferably 10 to 45 μm. When the particle size of the thermal spray powder is large, the porosity of the base layer formed by gas spraying is increased. In addition, if the particle size of the sprayed powder is small, clogging of the jet port called the port, which supplies the sprayed powder to gas or plasma, is likely to occur, and it takes time to form a sprayed coating with an arbitrary film thickness. Cost is likely to increase.
次にＭ−Ｃｒ−Ａｌ−Ｙ系合金からなる下地層上に、安定化ＺｒＯ２系耐食性被膜を形成する。 Next, a stabilized ZrO 2 -based corrosion resistant coating is formed on the underlayer made of the M—Cr—Al—Y alloy.
安定化ＺｒＯ２系耐食性被膜は、プラズマ溶射法によって形成することができる。プラズマ溶射法としては大気圧プラズマ溶射法、真空プラズマ溶射法等の種々の方法を用いることが可能である。この際に用いる溶射粉末には、安定化ＺｒＯ２粉末を使用することが好ましい。なお耐食性被膜の形成は、プラズマ溶射以外の溶射技術（例えばガス溶射）、コールドスプレー、エアロゾルデポジション法等の方法で形成することも可能である。 The stabilized ZrO 2 -based corrosion resistant coating can be formed by a plasma spraying method. As the plasma spraying method, various methods such as an atmospheric pressure plasma spraying method and a vacuum plasma spraying method can be used. It is preferable to use stabilized ZrO 2 powder as the thermal spraying powder used at this time. The corrosion resistant coating can be formed by a spraying technique other than plasma spraying (for example, gas spraying), a cold spray, an aerosol deposition method, or the like.
安定化ＺｒＯ２粉末の平均粒径は１０〜７５μｍ、１０〜５３μｍ、特に１０〜４５μｍであることが好ましい。安定化ＺｒＯ２粉末の平均粒径が大きいと、プラズマ溶射によって形成される耐食性被膜の気孔率が高くなる。また安定化ＺｒＯ２粉末の平均粒径が小さいと溶射粉末をプラズマに供給する噴出口（ポート）の詰まりが発生しやすくなり、任意の膜厚の溶射被膜の形成に時間がかかり、結果的に溶射コストが高くなり易い。 The average particle size of the stabilized ZrO 2 powder is preferably 10 to 75 μm, 10 to 53 μm, particularly preferably 10 to 45 μm. When the average particle size of the stabilized ZrO 2 powder is large, the porosity of the corrosion-resistant coating formed by plasma spraying is increased. In addition, if the average particle size of the stabilized ZrO 2 powder is small, clogging of the spray port (port) for supplying the sprayed powder to the plasma is likely to occur, and it takes time to form a sprayed coating having an arbitrary film thickness. Thermal spraying cost tends to be high.
続いて安定化ＺｒＯ２系耐食性被膜上に、封孔剤層を形成する。 Subsequently, a sealing agent layer is formed on the stabilized ZrO 2 -based corrosion resistant coating.
封孔剤層の形成は、例えば上記した封孔剤を含むペーストやスラリーを刷毛塗りやスプレー等の方法で耐食性被膜上に塗布し、必要に応じてさらに乾燥させる。このようにして封孔剤層を形成することができる。なお、スパッタリング、溶射等、封孔剤粉末が耐食性被膜から脱落しない方法であれば他の方法を採用することも可能である。 For forming the sealing agent layer, for example, a paste or slurry containing the sealing agent described above is applied onto the corrosion-resistant coating by a method such as brushing or spraying, and further dried as necessary. In this way, a sealant layer can be formed. It should be noted that other methods may be employed as long as the sealing agent powder does not fall off the corrosion-resistant coating, such as sputtering and thermal spraying.
このようにして作製した高温部材の封孔剤層は、封孔剤粉末が耐食性被膜表面に付着した状態であり、未だ完全に気孔を塞いだ状態とはなっていないが、この状態で使用箇所に設置することが可能である。つまり、使用が開始されると高温雰囲気に晒されることになり、その熱によって封孔剤が軟化流動して、耐食性被膜表面に存在する気孔を埋めるようになるためである。 The sealant layer of the high temperature member thus produced is in a state where the sealant powder is adhered to the surface of the corrosion-resistant coating, and is not yet in a state of completely closing the pores, Can be installed. That is, when the use is started, it is exposed to a high temperature atmosphere, and the heat causes the sealing agent to soften and flow to fill pores existing on the surface of the corrosion-resistant coating.
本発明の高温部材を作製するに当たり、封孔剤層を乾燥させた後（且つ、実使用の前）に焼成を行ってもよい。焼成条件としては、例えば３００〜１０００℃で１０分〜２時間が好ましい。実使用の前に予め焼成しておくことにより、移送中や使用箇所への設置の際に、封孔剤層が脱落したり、破損したりすることを防止できる。 In producing the high-temperature member of the present invention, firing may be performed after the sealant layer is dried (and before actual use). As firing conditions, for example, 10 to 2 hours at 300 to 1000 ° C. is preferable. By firing in advance before actual use, it is possible to prevent the sealant layer from falling off or being damaged during transfer or installation at the place of use.
以下、実施例に基づいて、本発明を詳細に説明する。
［封孔剤の調製］
表１は本発明の封孔剤の実施例（試料Ｎｏ．１〜６）を示している。
Hereinafter, based on an Example, this invention is demonstrated in detail.
[Preparation of sealant]
Table 1 shows Examples (Sample Nos. 1 to 6) of the sealant of the present invention.
各試料は次のようにして作製した。まず表中の組成となるように調合したガラスバッチを１３００℃で１時間溶融した。次いでこれをフィルム状に成形した後、粉砕、分級して平均粒径５０μｍのガラス粉末からなる封孔剤を得た。 Each sample was produced as follows. First, a glass batch prepared to have the composition in the table was melted at 1300 ° C. for 1 hour. Next, after forming this into a film, it was pulverized and classified to obtain a sealing agent made of glass powder having an average particle size of 50 μm.
なお軟化点は、示差熱分析装置を用い、山根正之著「はじめてガラスを作る人のために」に記載の方法に準じて測定した。熱膨張係数は、試料を棒状にプレス成型し、８００℃で２０分間焼成した後、ディラトメーターにて得られた熱膨張曲線より３０〜３８０℃の平均線熱膨張係数として算出した。また各試料について、軟化点＋４０℃、３０分の条件で熱処理した後、光学顕微鏡観察により結晶の有無を観察した。その結果、何れの試料も結晶は析出しておらず、非晶質ガラスであることが確認された。
［高温部材の作製］
次に試料Ｎｏ．１のガラスを用いて高温部材（試料Ａ）を作製した。
The softening point was measured using a differential thermal analyzer in accordance with the method described by Masayuki Yamane, “For the first glass maker”. The thermal expansion coefficient was calculated as an average linear thermal expansion coefficient of 30 to 380 ° C. from a thermal expansion curve obtained by a dilatometer after the sample was press-molded into a rod shape and baked at 800 ° C. for 20 minutes. Each sample was heat-treated at a softening point of + 40 ° C. for 30 minutes, and then observed for the presence of crystals by an optical microscope. As a result, no crystal was precipitated in any of the samples, and it was confirmed that the sample was amorphous glass.
[Production of high-temperature components]
Next, sample no. A high temperature member (sample A) was prepared using the glass No. 1.
試料Ａは次のようにして作製した。まずＳＵＳ３１０Ｓ基材を脱脂、洗浄後、ブラスト処理を行い、Ｃｏ−Ｎｉ−Ｃｒ−Ａｌ−Ｙ系合金からなる平均粒径１０〜４５μｍの合金粉末を高速フレーム溶射し、耐高温酸化性・耐高温腐食性に優れた下地層（Ｃｏ−Ｎｉ−Ｃｒ−Ａｌ−Ｙ合金層）を形成した。下地層の膜厚は均一で２００〜４００μｍであった。なお下地層の膜厚は、マイクロメーターにて測定した。また膜厚の調整は、まず溶射装置を基材と平行に移動させて溶射し、一回の溶射でどの程度の膜厚が得られるかをマイクロメーターで測定し、これを基にして溶射の回数を調節することにより行った。 Sample A was prepared as follows. First, SUS310S base material is degreased, washed, and then subjected to blasting, and high-speed flame spraying is performed on an alloy powder having an average particle size of 10 to 45 μm made of a Co—Ni—Cr—Al—Y alloy to provide high temperature oxidation resistance and high temperature resistance. A base layer (Co—Ni—Cr—Al—Y alloy layer) having excellent corrosivity was formed. The thickness of the underlayer was uniform and was 200 to 400 μm. The film thickness of the underlayer was measured with a micrometer. The film thickness can be adjusted by first moving the thermal spraying device parallel to the substrate and spraying it, and measuring with a micrometer how much film thickness can be obtained with a single spray. This was done by adjusting the number of times.
次に、平均粒径１０〜４５μｍの８％Ｙ２Ｏ３−ＺｒＯ２粉末を、下地層上に大気圧プラズマ溶射して耐食性被膜を形成した。耐食性被膜の膜厚は均一で５０〜２００μｍであった。なお耐食性被膜の膜厚の調整及び測定はＣｏ−Ｎｉ−Ｃｒ−Ａｌ−Ｙ合金を溶射する際と同様の方法で行った。 Next, 8% Y 2 O 3 —ZrO 2 powder having an average particle diameter of 10 to 45 μm was sprayed on the underlayer with atmospheric pressure plasma to form a corrosion-resistant coating. The film thickness of the corrosion-resistant film was uniform and was 50 to 200 μm. The adjustment and measurement of the film thickness of the corrosion-resistant coating were performed in the same manner as when the Co—Ni—Cr—Al—Y alloy was sprayed.
続いて以下の方法で封孔剤層を耐食性被膜上に形成した。まずシリコーン樹脂と試料Ｎｏ．１の封孔剤を混ぜ、封孔剤ペーストを作製した。次に耐食性被膜上に封孔剤ペーストを刷毛塗りによって塗布した後、８００℃で４日間焼成した。このようにして試料Ａを得た。 Subsequently, a sealant layer was formed on the corrosion-resistant film by the following method. First, silicone resin and sample no. 1 sealant was mixed to prepare a sealant paste. Next, a sealant paste was applied onto the corrosion-resistant film by brushing and then baked at 800 ° C. for 4 days. A sample A was thus obtained.
また対比のために高温部材試料Ｂを用意した。 A high temperature member sample B was prepared for comparison.
試料Ｂは次のようにして作製した。まず試料Ａと同様にして基材上に下地層及び耐食被膜を形成した。次にＢ２Ｏ３ ３２質量％、Ｎａ２Ｏ ６８％の組成となるように調製したガラス原料（ホウ酸及び炭酸ナトリウムの混合物）を耐食被膜上に塗布した後、８００℃で４時間焼成することによって試料Ｂを得た。 Sample B was prepared as follows. First, in the same manner as Sample A, an underlayer and a corrosion-resistant film were formed on a substrate. Next, a glass raw material (mixture of boric acid and sodium carbonate) prepared to have a composition of 32% by mass of B 2 O 3 and 68% of Na 2 O is applied on the corrosion-resistant coating and then baked at 800 ° C. for 4 hours. A sample B was obtained.
さらに封孔剤の反応性を判断するための基準として、下地層及び耐食性被膜のみを形成した試料Ｃを用意した。なお試料Ｃは、封孔剤層等を形成しないことを除き、試料Ａと同様にして作製した。 Further, as a reference for judging the reactivity of the sealing agent, a sample C on which only an underlayer and a corrosion-resistant film were formed was prepared. Sample C was prepared in the same manner as Sample A, except that no sealant layer or the like was formed.
このようにして得られた試料Ａ及びＢについて、被膜への浸透性及び反応性を評価した。結果を図１〜図３に示す。なお図４は、試料ＣのＳＥＭ観察及びＥＤＳ分析の結果である。 The samples A and B thus obtained were evaluated for permeability and reactivity into the coating. The results are shown in FIGS. FIG. 4 shows the results of SEM observation and EDS analysis of Sample C.
図１〜図２から明らかなように、試料Ｎｏ．１のＢ２Ｏ３−ＺｎＯ系非晶質ガラスからなる封孔剤を用いた試料Ａは、気孔への浸透性に優れており、また下地層との反応が殆ど見られなかった。これに対して試料Ｂは、図３から明らかなように、下地層と強く反応していることが確認された。これらの事実は、本発明の封孔剤が高い封孔性を有しており、また被膜を腐食させることがなく長期安定性に優れることを示している。 As is clear from FIG. 1 and FIG. Sample A using a sealing agent made of 1 B 2 O 3 —ZnO-based amorphous glass was excellent in permeability to pores, and hardly reacted with the underlayer. On the other hand, it was confirmed that the sample B reacted strongly with the underlayer as apparent from FIG. These facts show that the sealing agent of the present invention has high sealing properties and is excellent in long-term stability without corroding the coating.
なお浸透性は、切断した試料を樹脂に包埋し、切断面を研磨した後、切断面をＳＥＭ（走査電子顕微鏡）観察及びＥＤＳ（エネルギー分散型Ｘ線分析）分析を行った。なお、耐食性被膜内の全ての気孔が外部と貫通しているわけではない。従って、独立気孔が存在していても問題はない。 For the permeability, the cut sample was embedded in a resin, the cut surface was polished, and then the cut surface was subjected to SEM (scanning electron microscope) observation and EDS (energy dispersive X-ray analysis) analysis. Note that not all pores in the corrosion-resistant coating penetrate through the outside. Therefore, there is no problem even if independent pores exist.
本発明の封孔剤を使用した耐食性被膜は、高温燃焼ガスから、蒸気や空気等の流体を介して運動エネルギーや熱エネルギーを回収して発電を行う火力発電のタービンや伝熱管の保護膜として用いることが好ましい。具体的には、ガスタービン発電、石炭火力発電、石炭ガス化複合発電、石油火力発電、廃棄物発電、地熱発電等のタービンや伝熱管などの保護膜として好適である。ただし、これらに限定されるものでなく、各種エンジン等などの保護膜としても好適である。また本発明の高温部材は、ガスタービン発電、石炭火力発電、石炭ガス化複合発電、石油火力発電、廃棄物発電、地熱発電等のタービンや伝熱管、或いは各種エンジン等として好適である。 The corrosion-resistant coating using the sealant of the present invention is a protective film for a thermal power generation turbine or heat transfer tube that recovers kinetic energy or thermal energy from a high-temperature combustion gas via a fluid such as steam or air. It is preferable to use it. Specifically, it is suitable as a protective film for turbines and heat transfer tubes of gas turbine power generation, coal thermal power generation, coal gasification combined power generation, oil thermal power generation, waste power generation, geothermal power generation, and the like. However, the present invention is not limited to these, and is also suitable as a protective film for various engines. The high-temperature member of the present invention is suitable as a turbine or heat transfer tube for various types of engines such as gas turbine power generation, coal-fired power generation, coal gasification combined power generation, oil-fired power generation, waste power generation, and geothermal power generation.
１ 封孔剤
２ 耐食性被膜
３ 下地層
４ Ａｌ２Ｏ３過剰層
５ 樹脂
1 sealing agent 2 corrosion-resistant film 3 underlayer 4 Al 2 O 3 over layer 5 resin
Claims (9)
The method for producing a high-temperature member according to claim 8, further comprising a step of baking after applying the sealant coating solution.
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| CN201680052787.3A CN108025955A (en) | 2015-09-11 | 2016-09-02 | Hole sealing agent, hole sealing agent coating fluid, corrosion resistance coating, the manufacture method of high-temperature component and high-temperature component |
| PCT/JP2016/075826 WO2017043423A1 (en) | 2015-09-11 | 2016-09-02 | Sealing agent, sealing agent coating solution, corrosion-resistant coating film, high-temperature member, and method for producing high-temperature member |
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