JPS6164867A - Glass reinforced thermal spraying material - Google Patents
Glass reinforced thermal spraying materialInfo
- Publication number
- JPS6164867A JPS6164867A JP59183777A JP18377784A JPS6164867A JP S6164867 A JPS6164867 A JP S6164867A JP 59183777 A JP59183777 A JP 59183777A JP 18377784 A JP18377784 A JP 18377784A JP S6164867 A JPS6164867 A JP S6164867A
- Authority
- JP
- Japan
- Prior art keywords
- glass
- thermal spraying
- ceramic
- spraying material
- powder
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/10—Oxides, borides, carbides, nitrides or silicides; Mixtures thereof
- C23C4/11—Oxides
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Coating By Spraying Or Casting (AREA)
Abstract
Description
【発明の詳細な説明】 で強化し、緻密にした耐摩耗性の溶射材に関する。[Detailed description of the invention] It relates to abrasion-resistant thermal sprayed materials that are reinforced and densified.
従」U丸歯
溶射材はアルミナ、ジルコニア等のセラミック粉末、高
融点の金属粉末、これらの混合物が一般的である。これ
らの溶射材の溶射被膜の構造は溶射フレーム中で溶融し
た粒子が積層したものであるが、積層間にはかなりの気
孔が存在しているため強度や耐摩耗性は成形体に較べ非
常に劣っている。The thermal spraying materials for round teeth are generally ceramic powders such as alumina and zirconia, high melting point metal powders, and mixtures thereof. The structure of the thermal spray coating of these thermal spray materials is that particles melted in the thermal spray flame are laminated, but since there are considerable pores between the laminated layers, the strength and abrasion resistance are much lower than that of molded products. Inferior.
良!!L!!2JL部
本発明は溶射被膜が緻密で耐摩耗性に優れた溶射材を提
供することを目的とする。good! ! L! ! 2JL Section An object of the present invention is to provide a thermal spray material with a dense thermal spray coating and excellent wear resistance.
l豆立l真−11
本発明はアルミナ、ジルコニア等ノ融点が1600℃以
上のセラミック粉末とホウケイ醜ガラス等の融点が90
0°C以下のガラス粉末とを前者70〜90重量%(以
下%は重量基準)、後者lO〜30%に混合し、造粒し
た溶射材である。The present invention uses ceramic powder such as alumina, zirconia, etc., which has a melting point of 1600°C or higher, and porcelain glass, etc., which has a melting point of 90°C.
It is a thermal spray material made by mixing 70 to 90% by weight of the former and 10 to 30% of the latter and granulating the glass powder at 0°C or lower.
この溶射材を用いた溶射被膜はセラミック粒子が溶融し
、積層して生じた気孔に低融点、低粘度のガラス相が充
填した構造をなしている。セラミック相とガラス相とが
別々の相をなしていることが一つの特徴である。そのた
めにはセラミック材は融点が高く、ガラス材は融点が低
いことが必要である0両者の融点の差が小さいと両者か
に充填されるものであり、そのため低粘度であることが
必要である。A thermal spray coating using this thermal spray material has a structure in which ceramic particles are melted and stacked to form pores, which are filled with a glass phase having a low melting point and low viscosity. One of the characteristics is that the ceramic phase and the glass phase are separate phases. To do this, the ceramic material must have a high melting point, and the glass material must have a low melting point.0 If the difference in melting point between the two is small, both will be filled, so it is necessary to have a low viscosity. .
本発明で使用できる融点が1900 ’O以上のセラミ
ック材料としてはアルミナ、ジルコニア、マグネシャス
ピネノイMg0−AR,z03等)、チタン酸アルミ、
ムライト等を挙げることができる。Ceramic materials with a melting point of 1900'O or higher that can be used in the present invention include alumina, zirconia, magnetic spinenoy (Mg0-AR, z03, etc.), aluminum titanate,
Mullite etc. can be mentioned.
融点が900℃以下で本発明に好適なガラス材料として
はホウケイ酸ガラス、リン酸ガラスである。これらの組
成範囲を示せば、
ホウケイ酸ガラス
B2 03 20〜50%
5i02 0〜50%
CaO5〜15%
Na2O5〜25%
A又 203 <5%
PbO5〜50%
リン酸ガラス
P2O530〜70%
Ca0 5〜15%
Na2O5〜25%
BaO10〜50%
両者の混合割合はガラス成分が10%未満(セラミック
成分が90%を越)では気孔を充填し、被膜を緻密にす
るに不十分であり、30%を越えると被膜の抗折力、耐
摩耗性等の特性が低下する。Glass materials having a melting point of 900° C. or less and suitable for the present invention include borosilicate glass and phosphate glass. These composition ranges are as follows: borosilicate glass B2 03 20-50% 5i02 0-50% CaO 5-15% Na2O 5-25% A or 203 <5% PbO 5-50% phosphate glass P2O 530-70% Ca0 5- 15% Na2O5-25% BaO10-50% The mixing ratio of both is that if the glass component is less than 10% (ceramic component is more than 90%), it is insufficient to fill the pores and make the coating dense. If it exceeds this, the properties such as transverse rupture strength and abrasion resistance of the coating will deteriorate.
両者の混合、造粒についてはセラミック粉末は10pm
以下に粉砕し、またガラスは溶融して製造したフリット
を粉砕してLO4rn以下程度にし、これらをよく混合
し、PVA、CMC,コンスターチ等を1次バインダに
して造粒する。造粒は例えばスプレードライヤー、ヘン
シルミキサー等により行なう0粒子の大きさは水プラズ
マ装置の場合88〜10pm、ガスプラズマ装置の場合
53〜lO用m程度が適する。For mixing and granulation of both, ceramic powder is 10pm.
The glass is pulverized as follows, and the frit produced by melting the glass is pulverized to about LO4rn or less, mixed well, and granulated using PVA, CMC, cornstarch, etc. as a primary binder. Granulation is carried out using, for example, a spray dryer, a Henshil mixer, etc. The size of the zero particles is suitably 88 to 10 pm in the case of a water plasma device, and 53 to 10 m in the case of a gas plasma device.
1厘1
セラミック材として電融アルミナ(AJ120コ97%
)、ガラス材として次の組成のホウケイ酸ガラスを用い
た。1 liter 1 Electro-fused alumina (AJ120 97%) as a ceramic material
), borosilicate glass having the following composition was used as the glass material.
B、203 37.1% Na2O15,8%S
i 02 37.I A1203 1JCa
O7,9K2O0,7
電融アルミナは10ga+以下に粉砕、ガラスは工OJ
Lm以下に粉砕し、前者90%、後者20%の割合に混
合し、コーンスターチを一次バインダーとし。B, 203 37.1% Na2O15,8%S
i 02 37. I A1203 1JCa
O7,9K2O0,7 Fused alumina is crushed to 10ga+ or less, glass is milled OJ
Pulverized to less than Lm and mixed at a ratio of 90% of the former and 20% of the latter, using cornstarch as the primary binder.
スラリー濃度30%、スラリー供給量20文/+in、
アトマイザ−回転数1200Or、p、Il、、乾tl
&温度f50’cで、88〜IOHの粒子に造粒した。Slurry concentration 30%, slurry supply amount 20 sentences/+in,
Atomizer - rotation speed 1200Or, p, Il, dry tl
& granulated into particles of 88 to IOH at a temperature of f50'c.
この粒子を用い、公知の水プラズマ溶射機により5S−
41基材上に溶射し、その被膜の特性を測定した。比較
として電融アルミナの溶射被膜を示す。Using these particles, 5S-
No. 41 was thermally sprayed onto a substrate, and the properties of the coating were measured. For comparison, a sprayed coating of fused alumina is shown.
本発明 電融アルミナ
真比重 3.21 3.91
見掛比重 3.18 3.B:1余気孔率
8.9 12.2開気孔率 5.5
8.9抗折力 3.91 kg/lIm
’ 1.99摩擦摩耗 0.006 g/cr
n’ 0.230摩擦摩耗はポール板に圧子をと
りつけ
回転させ被膜の重量減少を求めた。Present invention Fused alumina True specific gravity 3.21 3.91 Apparent specific gravity 3.18 3. B: 1 remaining porosity 8.9 12.2 open porosity 5.5
8.9 Transverse rupture strength 3.91 kg/lIm
' 1.99 Frictional wear 0.006 g/cr
n' 0.230 Frictional wear was measured by attaching an indenter to a pole plate and rotating it to determine the weight loss of the coating.
え監立分」
本発明によればセラミックのもつ特性を殆んど失なうこ
となく、上記結果が示すように抗折力、#摩耗性を大幅
に改善することができる。According to the present invention, transverse rupture strength and abrasion resistance can be significantly improved, as shown by the above results, without losing much of the characteristics of ceramics.
Claims (3)
0重量%と融点が900℃以下のガラス粉末10〜30
重量%とを混合、造粒してなるガラス強化 溶射材。(1) Ceramic powder 70-9 with a melting point of 1600°C or higher
0% by weight and a glass powder with a melting point of 900°C or less 10-30
A glass-reinforced thermal spray material made by mixing and granulating % by weight.
シヤスピネルである特許請求の範囲第1項記載のガラス
強化溶射材。(2) The glass-reinforced thermal spray material according to claim 1, wherein the ceramic powder is alumina, zirconia, or magnesia spinel.
求の範囲第1項記載のガラス強化溶射材。(3) The glass reinforced thermal spray material according to claim 1, wherein the glass powder is borosilicate glass powder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59183777A JPS6164867A (en) | 1984-09-04 | 1984-09-04 | Glass reinforced thermal spraying material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59183777A JPS6164867A (en) | 1984-09-04 | 1984-09-04 | Glass reinforced thermal spraying material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6164867A true JPS6164867A (en) | 1986-04-03 |
JPS6366899B2 JPS6366899B2 (en) | 1988-12-22 |
Family
ID=16141763
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59183777A Granted JPS6164867A (en) | 1984-09-04 | 1984-09-04 | Glass reinforced thermal spraying material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6164867A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63274681A (en) * | 1987-05-01 | 1988-11-11 | Inax Corp | Inorganic building material having ceramics-glass composite film and its production |
JPH04164874A (en) * | 1990-10-26 | 1992-06-10 | Tomoaki Murata | Production of construction material |
EP0796929A1 (en) * | 1996-03-21 | 1997-09-24 | United Technologies Corporation | Abrasive Seal coatings |
JP2009035774A (en) * | 2007-08-01 | 2009-02-19 | Nippon Tokushu Rozai Kk | Method for smoothing surface of thermal-sprayed body |
JP2009511743A (en) * | 2005-10-11 | 2009-03-19 | コミッサリア タ レネルジー アトミーク | Stable joint formed by thermal spraying |
JP2014019876A (en) * | 2012-07-12 | 2014-02-03 | Yoshino:Kk | Thermal barrier material and manufacturing method of the same, and thermal barrier coating film and formation method of the same |
JP2015002306A (en) * | 2013-06-18 | 2015-01-05 | 富士電機株式会社 | Insulating substrate and manufacturing method therefor |
JP2018012852A (en) * | 2016-07-19 | 2018-01-25 | 株式会社東芝 | Aggregate, production method thereof, and formation method of coating sheet using aggregate |
JP2018199856A (en) * | 2017-05-29 | 2018-12-20 | 日立造船株式会社 | Manufacturing method of thermal spray material, thermal spray material, thermal spray method and thermal spray product |
-
1984
- 1984-09-04 JP JP59183777A patent/JPS6164867A/en active Granted
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63274681A (en) * | 1987-05-01 | 1988-11-11 | Inax Corp | Inorganic building material having ceramics-glass composite film and its production |
JPH04164874A (en) * | 1990-10-26 | 1992-06-10 | Tomoaki Murata | Production of construction material |
EP0796929A1 (en) * | 1996-03-21 | 1997-09-24 | United Technologies Corporation | Abrasive Seal coatings |
JP2009511743A (en) * | 2005-10-11 | 2009-03-19 | コミッサリア タ レネルジー アトミーク | Stable joint formed by thermal spraying |
JP2009035774A (en) * | 2007-08-01 | 2009-02-19 | Nippon Tokushu Rozai Kk | Method for smoothing surface of thermal-sprayed body |
JP2014019876A (en) * | 2012-07-12 | 2014-02-03 | Yoshino:Kk | Thermal barrier material and manufacturing method of the same, and thermal barrier coating film and formation method of the same |
JP2015002306A (en) * | 2013-06-18 | 2015-01-05 | 富士電機株式会社 | Insulating substrate and manufacturing method therefor |
JP2018012852A (en) * | 2016-07-19 | 2018-01-25 | 株式会社東芝 | Aggregate, production method thereof, and formation method of coating sheet using aggregate |
JP2018199856A (en) * | 2017-05-29 | 2018-12-20 | 日立造船株式会社 | Manufacturing method of thermal spray material, thermal spray material, thermal spray method and thermal spray product |
Also Published As
Publication number | Publication date |
---|---|
JPS6366899B2 (en) | 1988-12-22 |
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