JPH037884A - Protective tube for measuring temperature of molten metal of nonferrous metal - Google Patents
Protective tube for measuring temperature of molten metal of nonferrous metalInfo
- Publication number
- JPH037884A JPH037884A JP14255189A JP14255189A JPH037884A JP H037884 A JPH037884 A JP H037884A JP 14255189 A JP14255189 A JP 14255189A JP 14255189 A JP14255189 A JP 14255189A JP H037884 A JPH037884 A JP H037884A
- Authority
- JP
- Japan
- Prior art keywords
- ceramic particles
- metal
- titanium
- composite material
- protective tube
- 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.)
- Pending
Links
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 41
- 239000002184 metal Substances 0.000 title claims abstract description 41
- 230000001681 protective effect Effects 0.000 title claims abstract description 22
- 239000000919 ceramic Substances 0.000 claims abstract description 39
- 239000002245 particle Substances 0.000 claims abstract description 35
- 239000002131 composite material Substances 0.000 claims abstract description 22
- 229910001069 Ti alloy Inorganic materials 0.000 claims abstract description 10
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000010936 titanium Substances 0.000 claims abstract description 9
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 9
- 239000012535 impurity Substances 0.000 claims abstract description 4
- 238000009529 body temperature measurement Methods 0.000 claims description 3
- -1 ferrous metals Chemical class 0.000 claims description 3
- 150000002739 metals Chemical class 0.000 abstract description 9
- 238000002844 melting Methods 0.000 abstract description 7
- 230000008018 melting Effects 0.000 abstract description 7
- 229910045601 alloy Inorganic materials 0.000 abstract description 2
- 239000000956 alloy Substances 0.000 abstract description 2
- 230000035939 shock Effects 0.000 abstract 2
- 230000000052 comparative effect Effects 0.000 description 8
- 230000003628 erosive effect Effects 0.000 description 8
- 239000010410 layer Substances 0.000 description 6
- 229910001018 Cast iron Inorganic materials 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 229910052581 Si3N4 Inorganic materials 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 235000019353 potassium silicate Nutrition 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- QYEXBYZXHDUPRC-UHFFFAOYSA-N B#[Ti]#B Chemical compound B#[Ti]#B QYEXBYZXHDUPRC-UHFFFAOYSA-N 0.000 description 1
- 101100258328 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) crc-2 gene Proteins 0.000 description 1
- 229910033181 TiB2 Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229910007948 ZrB2 Inorganic materials 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- VWZIXVXBCBBRGP-UHFFFAOYSA-N boron;zirconium Chemical compound B#[Zr]#B VWZIXVXBCBBRGP-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000005524 ceramic coating Methods 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001513 hot isostatic pressing Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910052574 oxide ceramic Inorganic materials 0.000 description 1
- 239000011224 oxide ceramic Substances 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Landscapes
- Measuring Temperature Or Quantity Of Heat (AREA)
- Waste-Gas Treatment And Other Accessory Devices For Furnaces (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明はアルミニウム、亜鉛、スズ及び鉛等の非鉄金属
溶湯の温度を測定する熱電対を溶湯から保護する非鉄金
属溶湯測温用保護管に関する。Detailed Description of the Invention [Field of Industrial Application] The present invention relates to a protection tube for measuring the temperature of molten nonferrous metals that protects thermocouples that measure the temperature of molten nonferrous metals such as aluminum, zinc, tin, and lead from the molten metal. .
〔従来の技術]
従来、非鉄金属溶湯測温用の保護管(以下、保護管とい
う)には、JIS FCD50等の鋳鉄が一般に多く使
用されている。しかしながら、−船釣に非鉄金属は鉄と
反応しやすいという性質があるため、非鉄金属溶湯と接
触する部分では保護管に著しい溶損が発生する。従って
、保護管を頻繁に交換する必要があり、寿命が短い。こ
のため、通常、保護管の表面にセラミックス層を設けて
保護管の溶損を抑制するようにしている。例えば、セラ
ミックス粒子である325メツシユ以下のアルミナに1
重量%の水ガラスと30重量%の水又はPVA (ポリ
ビニルアルコール)等のバインダを配合してよく混合し
た泥漿を、JTs FCD50鋳鉄製の保護管の表面に
ハケ塗りでコーティングした後十分に一乾燥させて、厚
さが約21のセラミックス層を形成する。このようにし
て得られたセラミックス被覆保護管は耐溶損性が優れて
いる。また、近年、非鉄金属溶湯に対して安定なセラミ
ックス材質である窒化ケイ素からなる保護管も使用され
ている。[Prior Art] Conventionally, cast iron such as JIS FCD50 is generally used for protection tubes for temperature measurement of molten nonferrous metals (hereinafter referred to as protection tubes). However, since non-ferrous metals used in boat fishing tend to react easily with iron, significant erosion occurs in the protective tubes at the portions that come into contact with molten non-ferrous metals. Therefore, the protection tube must be replaced frequently, and its lifespan is short. For this reason, a ceramic layer is usually provided on the surface of the protective tube to suppress melting and damage of the protective tube. For example, for alumina of 325 mesh or less, which is a ceramic particle,
After coating the surface of the JTs FCD50 cast iron protective tube with a brush, a slurry made by blending 30% by weight of water glass and 30% by weight of water or a binder such as PVA (polyvinyl alcohol) was coated with a brush, and then thoroughly dried. In this way, a ceramic layer having a thickness of approximately 21 mm is formed. The ceramic-coated protective tube thus obtained has excellent erosion resistance. Furthermore, in recent years, protective tubes made of silicon nitride, which is a ceramic material that is stable against molten nonferrous metals, have also been used.
[発明が解決しようとする課題]
しかしながら、上述した従来の非鉄金属溶湯測混用保護
管は以下に示す欠点を有する。先ず、セラミックス被覆
層を設けた保護管は、使用の過程でこのセラミックス層
が剥離しやすい。そして、セラミックス層が剥離したと
きには、鋳鉄製保護管が露出してこの保護管に著しい溶
損が発生するという問題点がある。[Problems to be Solved by the Invention] However, the conventional protection tube for measuring and mixing non-ferrous metal molten metal described above has the following drawbacks. First, in a protective tube provided with a ceramic coating layer, the ceramic layer is likely to peel off during the course of use. When the ceramic layer peels off, there is a problem in that the cast iron protective tube is exposed and significant melt damage occurs in the protective tube.
また、窒化ケイ素からなる保護管は耐溶損性は優れてい
るものの、基質がセラミックスであるため、脆いという
難点がある。このため、溶湯中へ地金を投入する場合又
は溶湯を攪拌する場合に、地金又は攪拌羽根が保護管に
衝突したときに、窒化けい素製保護管が容易に破損して
しまう。そうすると、溶湯を測温することができなくな
り、鋳造等の作業を中断する必要が生じ、作業性が悪%
>という問題点がある。Furthermore, although a protection tube made of silicon nitride has excellent corrosion resistance, it has the disadvantage of being brittle because its substrate is ceramic. For this reason, the silicon nitride protection tube is easily damaged when the metal ingot or the stirring blade collides with the protection tube when pouring the metal into the molten metal or stirring the molten metal. In this case, it becomes impossible to measure the temperature of the molten metal, and it becomes necessary to interrupt work such as casting, which reduces work efficiency.
>There is a problem.
本発明はかかる問題点に鑑みてなされたものであって、
非鉄金属溶湯に対する耐溶損性が優れていると共に、耐
衝撃性にも優れており、作業性を向上できる長寿命の非
鉄金属溶湯測温用保護管を提供することを目的とする。The present invention has been made in view of such problems, and includes:
It is an object of the present invention to provide a protective tube for temperature measurement of molten nonferrous metal that has excellent resistance to melting and damage to molten nonferrous metal, has excellent impact resistance, and has a long life and can improve workability.
[課題を解決するための手段]
本発明に係る非鉄金属溶湯測温用保護管は、少なくとも
溶湯と接触する部分がチタン又はチタン合金とセラミッ
クス粒子と不可避的不純物とからなる複合材料により形
成されており、前記セラミックス粒子の体積含有率が0
.1乃至50%であることを特徴とする。[Means for Solving the Problems] The protection tube for measuring the temperature of molten nonferrous metal according to the present invention has at least the portion that comes into contact with the molten metal formed of a composite material consisting of titanium or a titanium alloy, ceramic particles, and inevitable impurities. and the volume content of the ceramic particles is 0.
.. It is characterized by being 1 to 50%.
[作用コ
本発明においては、少なくとも溶湯と接触する部分がチ
タン又はチタン合金と所定のセラミックス粒子との複合
材料により形成されている。この複合材料は、非鉄金属
の溶湯に対して優れた耐溶損性を何すると共に耐衝撃性
にも優れたチタン又はチタン合金に、高強度且つ高硬度
のセラミックス粒子を添加したものであり、耐溶損性、
耐衝撃性及び耐摩耗性を兼備している。従って、この複
合材料で溶湯接触部を形成することにより、長寿命であ
り、作業性が優れた非鉄金属溶湯測温用の保護管が得ら
れる。[Function] In the present invention, at least the portion that comes into contact with the molten metal is formed of a composite material of titanium or a titanium alloy and predetermined ceramic particles. This composite material is made by adding high-strength and hard ceramic particles to titanium or titanium alloy, which has excellent corrosion resistance against molten nonferrous metals and also has excellent impact resistance. damage,
It has both impact resistance and abrasion resistance. Therefore, by forming the molten metal contact portion with this composite material, a protective tube for measuring the temperature of molten nonferrous metal can be obtained that has a long life and is excellent in workability.
次に、この複合材料を構成するセラミックス成分の体積
含有率及び平均粒径の限定理由について説明する。Next, the reason for limiting the volume content and average particle size of the ceramic components constituting this composite material will be explained.
複合材料中のセラミックス粒子の体積含有率が0.1%
未溝の場合は、複合材料の硬度及び耐摩耗性は極めて低
いものとなる。一方、セラミックス粒子の体積含有率が
50%を超えると、複合材料が脆性化するため、耐衝撃
性が劣′化し、割れやすくなる。このため、複合材料中
のセラミックス粒子の体積含有率は0.1乃至50%に
する。The volume content of ceramic particles in the composite material is 0.1%
If no grooves are formed, the hardness and wear resistance of the composite material will be extremely low. On the other hand, if the volume content of the ceramic particles exceeds 50%, the composite material becomes brittle, resulting in poor impact resistance and becoming susceptible to cracking. For this reason, the volume content of ceramic particles in the composite material is set to 0.1 to 50%.
また、複合材料中のセラミックス粒子の平均粒径が0.
01μm未満の場合は、マトリックスであるチタン又は
チタン合金中にセラミックス粒子を均一に分散させるこ
とが困難になり、安定した特性の複合材料を得にくくな
る。一方、セラミックス粒子の平均粒径が500μmを
超えると、セラミックス粒子間の間隔が大きくなるため
、複合材料の硬度が低下しやすい。そうすると、複合材
料の耐摩耗性も低下する。このため、複合材料中のセラ
ミックス粒子の平均粒径は0.Ol乃至500μmにす
ることが好ましい。Further, the average particle size of the ceramic particles in the composite material is 0.
If it is less than 0.01 μm, it becomes difficult to uniformly disperse the ceramic particles in the titanium or titanium alloy matrix, making it difficult to obtain a composite material with stable characteristics. On the other hand, when the average particle size of the ceramic particles exceeds 500 μm, the distance between the ceramic particles becomes large, so that the hardness of the composite material tends to decrease. This also reduces the wear resistance of the composite material. Therefore, the average particle size of the ceramic particles in the composite material is 0. It is preferable to set the thickness to 01 to 500 μm.
なお、本発明においては、その使用対象となる非鉄金属
は純A!及び純Zn等の純金属以外に、これらの金属の
合金も含むことは勿論である。In addition, in the present invention, the non-ferrous metal to be used is pure A! Of course, in addition to pure metals such as pure Zn, alloys of these metals are also included.
[実施例コ
次に、本発明の実施例についてその比較例と比較して説
明する。[Example] Next, an example of the present invention will be described in comparison with a comparative example.
先ず、平均粒径が35μmであり、5重量%のCOを含
有するチタン合金粉末と、平均粒径が15μmの炭化ケ
イ素(SiC)粉末とを下記第1表に示す割合で均一に
混合して原料とした。First, titanium alloy powder having an average particle size of 35 μm and containing 5% by weight of CO and silicon carbide (SiC) powder having an average particle size of 15 μm were uniformly mixed in the proportions shown in Table 1 below. Used as raw material.
この原料をゴム型に装入し、その中心に芯金を配置して
、加圧力が2トン/ cJの条件で冷間静水圧プレス(
CI P)加工を行った。これにより、タンマン管状の
圧粉体を得た。そして、この圧粉体を真空度が10−5
Torr、温度が1300°Cの真空炉中で焼結させる
ことにより、第1表に示す組成の複合材料からなる保護
管を製作した。この各保護管を実施例1乃至4及び比較
例1乃至3とした。This raw material was charged into a rubber mold, a core metal was placed in the center, and cold isostatic press (
CI P) processing was performed. As a result, a powder compact in the form of a Tamman tube was obtained. Then, the degree of vacuum of this powder compact is 10-5.
A protective tube made of a composite material having the composition shown in Table 1 was manufactured by sintering it in a vacuum furnace at a temperature of 1300°C. These protective tubes were designated as Examples 1 to 4 and Comparative Examples 1 to 3.
第1表
鋼製モールドを溶解させ、複合材料からなる保護管を製
作した。この各保護管を実施例5乃至9及び比較例4と
した。Table 1 A protective tube made of a composite material was manufactured by melting a steel mold. These protective tubes were designated as Examples 5 to 9 and Comparative Example 4.
第2表
次に、平均粒径が20μmであり、純度が99.7重量
%以上のチタン粉末と下記第2表に示す平均粒径のA1
□03粉末とを体積比で80 : 20 (セラミック
スの体積含有率20%)で混合して原料とした。Table 2 Next, titanium powder with an average particle size of 20 μm and a purity of 99.7% by weight or more and A1 with the average particle size shown in Table 2 below.
□03 powder was mixed at a volume ratio of 80:20 (volume content of ceramics: 20%) to prepare a raw material.
この原料を厚さが1龍のJIS 5S41鋼板で作られ
たモールドに封入し、加圧力が1トン/c11温度が1
250℃の条件で、熱間静水圧プレス(HI P)加工
を行って焼結させた。次いで、この焼結体及び鋼製モー
ルドの全体を濃塩酸溶液に浸漬して、次に、鋳鉄(FC
D 50)型保護管の表面に、325メツシユ以下のア
ルミナ粒子(69重量%)と、 1重量%の水ガラスと
、30重量%の水とを混合した泥漿をハケ塗りでコーテ
ィングした後、十分に乾燥させて厚さが約2■嘗のセラ
ミックス層を形成した。このセラミックス層被覆鋳鉄製
保護管を従来例1とした。また、窒化ケイ素製保護管を
従来例2とした。This raw material is sealed in a mold made of JIS 5S41 steel plate with a thickness of 1 dragon, and the pressure is 1 ton/c11 temperature is 1
Sintering was performed by hot isostatic pressing (HIP) at 250°C. Next, the entire sintered body and steel mold were immersed in a concentrated hydrochloric acid solution, and then cast iron (FC
After coating the surface of the D50 type protection tube with a slurry made by mixing alumina particles of 325 mesh or less (69% by weight), 1% by weight of water glass, and 30% by weight of water with a brush, apply thoroughly. It was dried to form a ceramic layer about 2 inches thick. This ceramic layer-coated cast iron protective tube was designated as Conventional Example 1. Further, a protection tube made of silicon nitride was used as Conventional Example 2.
上述した実施例、比較例及び従来例の各保護管に対し、
下記に示す試験を行ってその性能を調べた。For each protection tube of the above-mentioned example, comparative example, and conventional example,
The following tests were conducted to examine its performance.
■硬度試験
実施例、比較例及び従来例の各保護管のマイクロビッカ
ース硬度を測定した。(2) Hardness Test The micro-Vickers hardness of each protection tube of the Example, Comparative Example, and Conventional Example was measured.
■引張試験 引張試験機により伸びを測定した。■Tensile test Elongation was measured using a tensile tester.
■実用試験
実施例、比較例及び従来例の各保護管をアルミニウム合
金溶解炉(能力1トン)に浸漬させて、1000時間後
の溶損状況を調べた。(4) Practical Test The protective tubes of Examples, Comparative Examples, and Conventional Examples were immersed in an aluminum alloy melting furnace (capacity: 1 ton), and the state of melting damage after 1000 hours was investigated.
これらの試験結果をまとめて下記第3表に示す。The results of these tests are summarized in Table 3 below.
但し、溶損状況は保護管の表面における最大溶損量が0
.1■以下の場合を◎、0.1mmを超え0.3m■以
下の場合を0. 0.3mmを超える場合をΔで示した
。However, regarding the erosion condition, the maximum amount of erosion on the surface of the protection tube is 0.
.. ◎ if it is less than 1■, 0. if it is more than 0.1mm and less than 0.3m■. Cases exceeding 0.3 mm are indicated by Δ.
第3表(その1)
第3表(その2)
この第3表から明らかなように、実施例1乃至8はいず
れも溶損量が0.1m以下であり、割れも発生していな
い。一方、比較例3及び従来例2は伸びが0.2%以下
と極めて低く、地金投入時の接触により割れが発生した
。その他の比較例工、2゜4及び従来例1はいずれも溶
損量が0.1■■を超えており、耐溶損性が悪いもので
あった。Table 3 (Part 1) Table 3 (Part 2) As is clear from Table 3, in Examples 1 to 8, the amount of erosion was less than 0.1 m, and no cracking occurred. On the other hand, in Comparative Example 3 and Conventional Example 2, the elongation was extremely low at 0.2% or less, and cracks occurred due to contact when the metal was introduced. The other Comparative Examples, 2°4, and Conventional Example 1 all had an amount of erosion exceeding 0.1■■, and had poor erosion resistance.
なお、本発明において使用可能なセラミックスは上述の
SiC及びA1□03に限定されるものではなく、Cr
2O3、TiO2、ZrO2、MgO1Y203等の酸
化物等系セラミックス、S 13N4 、T iNs
B N及びAlN等の窒化物系セラミックス、WCzT
tCsBaC及びCrC2等の炭化物系セラミックス、
ZrB2及びTiB2等のホウ化物系セラミックス並び
にサイアロン等、種々のものを使用することができる。Note that the ceramics that can be used in the present invention are not limited to the above-mentioned SiC and A1□03, but include Cr
Oxide ceramics such as 2O3, TiO2, ZrO2, MgO1Y203, S13N4, TiNs
Nitride ceramics such as B N and AlN, WCzT
Carbide ceramics such as tCsBaC and CrC2,
Various materials can be used, such as boride ceramics such as ZrB2 and TiB2, and sialon.
また、これらのセラミックスを2種類以上混合して使用
することもできる。Moreover, two or more types of these ceramics can be mixed and used.
[発明の効果]
以上説明したように本発明によれば、非鉄金属溶湯測温
用保護管の少なくとも溶湯と接触する部分がチタン又は
チタン合金とセラミックス粒子との複合材料により形成
されているため、耐溶損性及び耐衝撃性の双方が優れた
保護管が得られる。[Effects of the Invention] As explained above, according to the present invention, at least the portion of the nonferrous metal molten metal temperature measuring protection tube that comes into contact with the molten metal is formed of a composite material of titanium or a titanium alloy and ceramic particles. A protective tube excellent in both erosion resistance and impact resistance can be obtained.
従って、この保護管を使用すれば、溶損が抑制されて寿
命が延長され、また地金投入時等の衝撃を受けても割れ
の発生が抑制され、作業性を著しく向上させることがで
きる。Therefore, if this protection tube is used, melting damage is suppressed and the service life is extended, and cracking is also suppressed even when subjected to impact such as when inserting ingots, and workability can be significantly improved.
Claims (2)
ン合金とセラミックス粒子と不可避的不純物とからなる
複合材料により形成されており、前記セラミックス粒子
の体積含有率が0.1乃至50%であることを特徴とす
る非鉄金属溶湯測温用保護管。(1) At least the part that comes into contact with the molten metal is made of a composite material consisting of titanium or titanium alloy, ceramic particles, and unavoidable impurities, and the volume content of the ceramic particles is 0.1 to 50%. A protective tube for temperature measurement of molten non-ferrous metals.
500μmであることを特徴とする請求項1に記載の非
鉄金属溶湯測温用保護管。(2) The protective tube for measuring the temperature of molten nonferrous metal according to claim 1, wherein the ceramic particles have an average particle size of 0.01 to 500 μm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14255189A JPH037884A (en) | 1989-06-05 | 1989-06-05 | Protective tube for measuring temperature of molten metal of nonferrous metal |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14255189A JPH037884A (en) | 1989-06-05 | 1989-06-05 | Protective tube for measuring temperature of molten metal of nonferrous metal |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH037884A true JPH037884A (en) | 1991-01-16 |
Family
ID=15317979
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14255189A Pending JPH037884A (en) | 1989-06-05 | 1989-06-05 | Protective tube for measuring temperature of molten metal of nonferrous metal |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH037884A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20130067285A (en) * | 2013-05-27 | 2013-06-21 | 한국토형와전 주식회사 | Environmental permeation block and method thereof |
-
1989
- 1989-06-05 JP JP14255189A patent/JPH037884A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20130067285A (en) * | 2013-05-27 | 2013-06-21 | 한국토형와전 주식회사 | Environmental permeation block and method thereof |
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