JPH0238144B2 - YOSHAZAI - Google Patents
YOSHAZAIInfo
- Publication number
- JPH0238144B2 JPH0238144B2 JP18529984A JP18529984A JPH0238144B2 JP H0238144 B2 JPH0238144 B2 JP H0238144B2 JP 18529984 A JP18529984 A JP 18529984A JP 18529984 A JP18529984 A JP 18529984A JP H0238144 B2 JPH0238144 B2 JP H0238144B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- thermal
- spraying
- thermal spray
- color
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000463 material Substances 0.000 claims description 30
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 24
- 239000007921 spray Substances 0.000 claims description 16
- 229910018072 Al 2 O 3 Inorganic materials 0.000 claims description 11
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 claims description 9
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- 238000007751 thermal spraying Methods 0.000 description 21
- 239000011787 zinc oxide Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- 238000005507 spraying Methods 0.000 description 10
- 238000000034 method Methods 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- LTPBRCUWZOMYOC-UHFFFAOYSA-N beryllium oxide Inorganic materials O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000002845 discoloration Methods 0.000 description 3
- 229910044991 metal oxide Inorganic materials 0.000 description 3
- 150000004706 metal oxides Chemical class 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 229910052614 beryl Inorganic materials 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 238000005524 ceramic coating Methods 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000007750 plasma spraying Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- FRWYFWZENXDZMU-UHFFFAOYSA-N 2-iodoquinoline Chemical compound C1=CC=CC2=NC(I)=CC=C21 FRWYFWZENXDZMU-UHFFFAOYSA-N 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000010975 amethyst Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004534 enameling Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-UHFFFAOYSA-N 0.000 description 1
- 239000010437 gem Substances 0.000 description 1
- 229910001751 gemstone Inorganic materials 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 239000010979 ruby Substances 0.000 description 1
- 229910001750 ruby Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 229910009116 xCuO Inorganic materials 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Paints Or Removers (AREA)
Description
【発明の詳細な説明】
(発明の対象)
本発明は溶射材に係り、特に耐食性、耐摩耗性
かつ変褪色しない安定性着色溶射材に関する。DETAILED DESCRIPTION OF THE INVENTION (Subject of the Invention) The present invention relates to a thermal spray material, and particularly to a stable colored thermal spray material that is corrosion resistant, wear resistant, and resistant to discoloration and fading.
(従来技術)
基材の表面を着色被覆する技術としてホウロウ
法は公知である。ホウロウ法は基材を加熱するた
めコンクリート、木材等には施工できない欠点が
ある。(Prior Art) The enamel method is known as a technique for coloring and coating the surface of a base material. The enameling method has the disadvantage that it cannot be applied to concrete, wood, etc. because it heats the base material.
この欠点を改善する技術として溶射法がある。
溶射法は基材の性質を変えることなく基材表面を
被覆できるのみならず、溶射材にセラミツクスを
用いることにより被覆に耐熱性、耐食性、耐摩耗
性を付与できる利点がある。 Thermal spraying is a technique to improve this drawback.
Thermal spraying has the advantage that not only can the surface of the substrate be coated without changing the properties of the substrate, but also heat resistance, corrosion resistance, and abrasion resistance can be imparted to the coating by using ceramics as the thermal spraying material.
上記の諸機能を有するほか、更に美観を与える
装飾性を具備した溶射被覆材は現在その数極めて
少い。たとえば黒色を呈するAl2O3・TiO2白色の
Al2O3、コバルトブルー色を呈するAl2O3・CoO
等数例が挙げられる程度である。 Currently, there are very few thermal spray coating materials that have the above-mentioned functions and also have decorative properties that add beauty. For example, Al 2 O 3・TiO 2 which exhibits black color
Al 2 O 3 , Al 2 O 3・CoO exhibiting cobalt blue color
An equal number of examples can be cited.
このように着色溶射材が極めて少い理由は溶射
実施の前後における溶射材の発色色調が必ずしも
同一ではないという事実によるものである。特に
セラミツクス溶射をプラズマ法によつて実施する
際にはプラズマ発生を還元性雰囲気で行うため、
通常の結晶格子状態に比べて酸素欠損が多くなり
これに起因する色吸収を生ずるため、溶射後のセ
ラミツクス被覆の全体的色調が溶射前のセラミツ
クスの色調と異なるようになると考えられる。し
たがつて溶射の結果得られる色調を溶射前の溶射
材の見掛けの色調から予想することは極めて困難
であり、溶射を実際に行なつてみないと不明であ
る場合が多い。 The reason why there is so little colored thermal spray material is due to the fact that the color tone of the thermal spray material before and after thermal spraying is not necessarily the same. In particular, when performing ceramic spraying using the plasma method, plasma is generated in a reducing atmosphere.
It is thought that the overall color tone of the ceramic coating after thermal spraying becomes different from the color tone of the ceramic coating before thermal spraying because there are more oxygen vacancies than in a normal crystal lattice state and this causes color absorption. Therefore, it is extremely difficult to predict the color tone obtained as a result of thermal spraying from the apparent color tone of the thermal spraying material before thermal spraying, and it is often unknown until thermal spraying is actually performed.
しかし溶射に当り、溶射後における溶射被覆の
色調を溶射前に予知しておき、希望の色調に合せ
た溶射材を開発することは重要である。 However, when performing thermal spraying, it is important to predict the color tone of the thermal spray coating before thermal spraying and to develop a thermal spray material that matches the desired color tone.
(発明の目的)
本発明は、上記のような溶射技術の問題点にか
んがみ、被溶射基材を損傷せず耐食性、耐摩耗性
をもちながら溶射被覆の色を調節しうる溶射材、
とくに建材等に要望の強い黄土色を発色する溶射
被覆材を提供することにある。(Object of the Invention) In view of the problems of thermal spraying technology as described above, the present invention provides a thermal spraying material that does not damage the substrate to be thermally sprayed, has corrosion resistance and wear resistance, and can adjust the color of the thermal spray coating.
The object of the present invention is to provide a thermal spray coating material that develops an ocher color, which is particularly desired for building materials.
(発明の構成)
本発明の溶射材は配合比において酸化銅
(CuO)1〜20重量%、酸化亜鉛(ZnO)5〜40
重量%、アルミナ(Al2O3)40〜94重量%から成
る溶射材にある。(Structure of the Invention) The thermal spray material of the present invention has a compounding ratio of 1 to 20% by weight of copper oxide (CuO) and 5 to 40% by weight of zinc oxide (ZnO).
% by weight, and a thermal spray material consisting of 40-94% by weight of alumina (Al 2 O 3 ).
一般に金属の酸化物はそれぞれ固有の色を有し
ていることは周知である。たとえばベリリウムの
酸化物BeOはそれ自体白色を呈するが、それが
Al2O3、SiO2等と化合物をつくる場合には、たと
えばベリルの組成である3BeO・Al2O3・6SiO2と
なればいわゆる緑柱石のもつ淡緑色を呈する。ま
たMnOはそれ自体緑色を呈し、これがCaO、
SiO2等と化合物をつくる場合にも緑色を呈する。
天然および人工宝石として知られるサフアイア、
ルビー、スピネル、クオーツ、アメジスト等もす
べて組成成分である金属酸化物の特有の発色によ
るものである。 It is well known that each metal oxide generally has a unique color. For example, beryllium oxide BeO itself is white;
When a compound is made with Al 2 O 3 , SiO 2 , etc., for example, 3BeO.Al 2 O 3.6SiO 2 , which has the composition of beryl, exhibits the pale green color of beryl. In addition, MnO itself exhibits a green color, which is similar to CaO.
It also appears green when it forms a compound with SiO 2 etc.
Saphire, known as a natural and artificial gemstone,
Ruby, spinel, quartz, amethyst, etc. are all due to the unique coloring of the metal oxides that are their compositional components.
しかるに、溶射材においては一般に高温におい
て溶射される。しかも溶射材は金属酸化物の一種
または二種以上の混合物あるいは化合物である。
これらが高温溶射、たとえばプラズマ溶射される
場合には前記した通り、プラズマの高温において
組成物の一部が酸化、還元、化合、相変態等、何
等かの変色的影響を受けるため溶射前の溶射材の
色調は、それが溶射された後において必ずしも溶
射前の色調と同一とは限らない。したがつて被溶
射体である基材に対するカラー溶射材の溶射の場
合においては仕上げ表面の溶射被覆の発色を予め
想定することは極めて困難である。 However, thermal spray materials are generally sprayed at high temperatures. Moreover, the thermal spray material is one or a mixture or compound of two or more metal oxides.
When these are subjected to high-temperature spraying, for example plasma spraying, as mentioned above, some of the compositions are affected by some discoloration such as oxidation, reduction, compounding, phase transformation, etc. at the high temperature of the plasma, so it is necessary to spray them before spraying. The color tone of the material after it has been sprayed is not necessarily the same as the color tone before it was sprayed. Therefore, in the case of spraying a colored thermal spray material onto a base material to be thermally sprayed, it is extremely difficult to predict in advance the color development of the thermal spray coating on the finished surface.
本発明は斯様な困難を解決し、特に黄土色系統
溶射材の組成を特定することにより溶射後の被覆
表面色調を予め想定できるようにしたものであ
る。 The present invention solves such difficulties and makes it possible to predict the coated surface color tone after thermal spraying in advance by specifying the composition of the ocher-based thermal spray material.
本溶射材は溶射対象物、とくに木材、コンクリ
ート等の建造物において美観を与える装飾効果を
目的とするものであり、したがつて特に耐熱性を
問題にしない個所に多く適用される。そのために
ZnOの添加を可能にするものであり、その量は、
5〜40重量%の広範囲にわたり可能である。ZnO
の添加によつてCuOの発色を濃厚にする効果があ
り、黄土色の濃度はZnOの5〜40重量%の範囲に
おいてZnOの添加量に正比例する。従来の溶射材
にはZnOを含有するものは見当らない点から、本
発明溶射材は新規な組成物であると思われる。 This thermal spraying material is intended to provide a decorative effect that gives a beautiful appearance to objects to be thermally sprayed, especially buildings made of wood, concrete, etc. Therefore, it is often applied to areas where heat resistance is not particularly an issue. for that
It enables the addition of ZnO, the amount of which is
A wide range of 5 to 40% by weight is possible. ZnO
The addition of CuO has the effect of deepening the coloration of CuO, and the ocher concentration is directly proportional to the amount of ZnO added in the range of 5 to 40% by weight of ZnO. Since no conventional thermal spraying material contains ZnO, the thermal spraying material of the present invention is considered to have a novel composition.
CuOの組成が1〜20重量%に限定され、また
ZnOの組成が5〜40重量%に限定される理由は上
記各限定値範囲を逸脱する領域では、目的とする
美観を有する黄土色とならないためである。CuO
とZnOを上記の範囲で、調整することにより、溶
射後の被覆着色における黄土色の濃度を調節でき
る。 The composition of CuO is limited to 1-20% by weight, and
The reason why the composition of ZnO is limited to 5 to 40% by weight is that in areas outside the above-mentioned limited value ranges, the desired aesthetic appearance cannot be obtained. CuO
By adjusting ZnO and ZnO within the above ranges, the ocher concentration in the coating coloring after thermal spraying can be adjusted.
Al2O3の組成が40〜94重量%に限定される理由
はAl2O3の組成変化に応じて溶射面の粗度および
硬度に変化を生じ、特にAl2O3組成が40重量%以
下では硬度不足を生じ、また90重量%以上では目
的とする色とならないからである。 The reason why the Al 2 O 3 composition is limited to 40 to 94% by weight is that the roughness and hardness of the sprayed surface change depending on the change in the Al 2 O 3 composition. If it is less than 90% by weight, the hardness will be insufficient, and if it is more than 90% by weight, the desired color will not be obtained.
本発明溶射材はその組成成分であるCuO、ZnO
およびAl2O3がそれぞれ微粒の単体において混合
された粉粒体、または一次バインダーで造粒され
た造粒物もしくは組成式:xCuO・yZnO・
zAl2O3(x=1〜20、y=5〜40、z=40〜94)
で表わされる溶融物粉粒体の態様のいずれにおい
ても可能である。 The thermal spraying material of the present invention has compositional components such as CuO and ZnO.
and Al 2 O 3 are mixed as single fine particles, or granules granulated with a primary binder, or composition formula: xCuO・yZnO・
zAl2O3 (x=1~20, y=5~40, z =40~94)
It is possible in any of the embodiments of the melt powder represented by.
実施例 1
粒度がそれぞれ50μm以下のCuO粉粒物10重量
部、ZnO粉粒物15重量部およびAl2O3粉粒物100
重量部を均一に混合した溶射材は茶灰色を呈する
粉粒物である。この溶射材をコンクリート基材上
にプラズマ溶射した結果、被覆溶射面は濃い黄土
色を呈する美麗な外観が与えられた。この溶射面
のマイクロビツカース硬度は750Kg/mm2であり、こ
れは溶射面として充分な硬度であつた。またこの
溶射面の耐食性、耐摩耗性、耐候性(変褪色性)
もホーロー等に比べ優れたものであり、実用上の
使用に充分耐えるものであつた。Example 1 10 parts by weight of CuO powder, 15 parts by weight of ZnO powder, and 100 parts of Al 2 O 3 powder, each having a particle size of 50 μm or less
The thermal spray material obtained by uniformly mixing parts by weight is a brownish-gray powder. As a result of plasma spraying this thermal spraying material onto a concrete base material, the coated sprayed surface was given a beautiful appearance with a dark ocher color. The micro-Vickers hardness of this thermal sprayed surface was 750 Kg/mm 2 , which was sufficient hardness for a thermal sprayed surface. In addition, this thermal sprayed surface has corrosion resistance, abrasion resistance, and weather resistance (discoloration resistance).
It was also superior to enamel, etc., and was sufficiently durable for practical use.
実施例 2
CuO=3重量部、ZnO=18重量部、Al2O3=80
重量部から成る粒度53〜10μmの混合溶射材は灰
黒色を有する溶射材である。これを木材建物外壁
にプラズマアーク溶射した結果、溶射後の被覆溶
射面の色調は明るい黄土色の美麗な外観を呈する
ものであつた。Example 2 CuO = 3 parts by weight, ZnO = 18 parts by weight, Al 2 O 3 = 80
The mixed thermal spray material having a particle size of 53 to 10 .mu.m in parts by weight is a thermal spray material having a grayish-black color. When this was plasma arc sprayed onto the outer wall of a wooden building, the color tone of the coated sprayed surface after spraying was bright ocher and had a beautiful appearance.
Claims (1)
(ZnO)5〜40重量%、アルミナ(Al2O3)40〜
94重量%から成る溶射材。1 Copper oxide (CuO) 1~20% by weight, zinc oxide (ZnO) 5~40% by weight, alumina (Al 2 O 3 ) 40~
A thermal spray material consisting of 94% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18529984A JPH0238144B2 (en) | 1984-09-06 | 1984-09-06 | YOSHAZAI |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18529984A JPH0238144B2 (en) | 1984-09-06 | 1984-09-06 | YOSHAZAI |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6164771A JPS6164771A (en) | 1986-04-03 |
JPH0238144B2 true JPH0238144B2 (en) | 1990-08-29 |
Family
ID=16168426
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18529984A Expired - Lifetime JPH0238144B2 (en) | 1984-09-06 | 1984-09-06 | YOSHAZAI |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0238144B2 (en) |
-
1984
- 1984-09-06 JP JP18529984A patent/JPH0238144B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS6164771A (en) | 1986-04-03 |
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