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JPH0131674B2 - - Google Patents
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JPH0131674B2 - - Google Patents

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Publication number
JPH0131674B2
JPH0131674B2 JP56096340A JP9634081A JPH0131674B2 JP H0131674 B2 JPH0131674 B2 JP H0131674B2 JP 56096340 A JP56096340 A JP 56096340A JP 9634081 A JP9634081 A JP 9634081A JP H0131674 B2 JPH0131674 B2 JP H0131674B2
Authority
JP
Japan
Prior art keywords
coating layer
coating
silicon carbide
boron nitride
melting point
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
Application number
JP56096340A
Other languages
Japanese (ja)
Other versions
JPS57210589A (en
Inventor
Susumu Inoe
Isao Sakashita
Kazunori Meguro
Kunio Hamaguchi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Coorstek KK
Original Assignee
Toshiba Ceramics Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Toshiba Ceramics Co Ltd filed Critical Toshiba Ceramics Co Ltd
Priority to JP9634081A priority Critical patent/JPS57210589A/en
Priority to US06/390,135 priority patent/US4485143A/en
Publication of JPS57210589A publication Critical patent/JPS57210589A/en
Publication of JPH0131674B2 publication Critical patent/JPH0131674B2/ja
Granted legal-status Critical Current

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  • Resistance Heating (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はAl、Pb等の低融点金属の溶解、保持
炉等に使用される浸漬ヒーターの保護管に関する
ものである。 近年、例えばAlを溶解し保持する方式として
熱源を浸漬加熱する内熱式のものが採用されるよ
うになつてきた。 然し乍ら、この方式のものは熱効率の著しい向
上にもかかわらず、ヒーターの保護管が、溶融金
属やその表面に浮遊する酸化防止剤によつて浸蝕
され、或いは著しい温度差に基づく熱衝撃によつ
て割れるこということが多かつた。これは一般に
は鋳鉄管に粘土質の被膜を施したものであるため
上述のような現象を起すものと思われる。又炭化
珪素質保護管も使用し得るが、炭化珪素は熱伝導
が良好であるにもかかわらず、耐スポーリング性
については必ずしも満足すべきものではなかつ
た。 本発明は炭化珪素質保護管の改良にかゝるもの
で、炭化珪素の高強度、高熱伝導性という特長を
生かし、且つこれに断熱耐蝕性を有するコーテイ
ングを施すことによつて解決したものである。即
ち、コーテイング材として窒化珪素或いは窒化ホ
ウ素を使用し、これを一層又は二層以上被覆し、
更にその厚さを0.3〜3.5mmの範囲に限定したもの
である。 窒化珪素結合の炭化珪素あるいは自己結合の炭
化珪素等の炭化珪素質成形体はその製造工程に基
因する残存熱歪は保護管として使用した場合、急
激な温度変化によつてマイクロクラツクを生じ、
これが成長して使用期間の不安定化を招いてい
る。材料の温度変化に耐え得る最大値は一般に次
式によつて表わされている。 ΔT=σf(1−ν)/Eα ΔT=温度変化の最大値、σf=平均破壊係数、
ν:ポアソン比、E:ヤング率、α:熱膨脹係数 この値は材料によつてほぼ一定しているから、
材料の熱衝撃破壊を防ぐにはその内部温度の差を
ΔT以下に抑えることが必要である。そのために
は材料の表面温度上昇速度を遅延させることが効
果的である。 この発明においては断熱材として優れ、且つ低
融点金属又はその酸化防止剤によつても侵蝕され
ない材料として窒化珪素、窒化ホウ素が好ましい
ことを見い出したものである。尚、このコーテイ
ング層は二層以上にした場合にはより効果が高ま
ることが明らかになつた。 これはコーテイング層内に溶湯が浸透した場
合、二層の境界面で浸透が抑制され内部コーテイ
ング層への浸透が大巾に遅延されるものであるこ
とが明らかになつた。 コーテイング方法は窒化珪素又は窒化ホウ素の
粉末をリン酸アルミ等の無機のバインダーを加え
てスリツプ状にし、吹きつけ或いは浸漬法によつ
て行なう。又、コーテイング層は厚ければよいと
いうものではなく、3.5mm以上ではコーテイング
層自体の強度が不充分となり易く剥離が起る。一
方、その厚さが0.3mm以下では断熱効果が期待で
きず、従つて好ましい膜厚の範囲は0.3〜3.5mmで
ある。 以下に本発明の実施例につき説明する。 実施例 1 再結晶炭化珪素質保護管を下記4種のコーテイ
ング層を施し、Al溶湯740℃の保持炉に挿入、抜
き取りを繰り返し、その寿命を測定した。 (1) コーテイング層を施さない。 (2) 外表面に窒化珪素をスプレーコーテイング。 (3) 外表面に窒化ホウ素をスプレーコーテイン
グ。 (4) 外表面にAl2O3をスプレーコーテイング。 尚、コーテイング材はそれぞれの粉末にリン酸
Alを粘結材として加えたもので、膜厚はいづれ
も1.5mmである。Al溶湯への挿入速度を30秒、抜
き取り速度を30秒としてこの操作を1日3回繰り
返し、その耐用日数を調べた結果、下記の通りで
あつた。
The present invention relates to a protective tube for an immersion heater used in melting and holding furnaces for low-melting metals such as Al and Pb. In recent years, for example, an internal heating method in which a heat source is immersed in heat has been adopted as a method for melting and retaining Al. However, despite the remarkable improvement in thermal efficiency of this method, the protective tube of the heater is corroded by molten metal and antioxidants floating on its surface, or is susceptible to thermal shock caused by significant temperature differences. It often broke. It is thought that the above-mentioned phenomenon occurs because this is generally a cast iron pipe coated with a clay coating. A silicon carbide protective tube may also be used, but although silicon carbide has good thermal conductivity, its spalling resistance is not necessarily satisfactory. The present invention relates to an improvement of a silicon carbide protection tube, and the problem was solved by taking advantage of silicon carbide's characteristics of high strength and high thermal conductivity, and applying a coating that has heat insulation and corrosion resistance to it. be. That is, silicon nitride or boron nitride is used as a coating material, and one or more layers of this are coated,
Furthermore, the thickness is limited to a range of 0.3 to 3.5 mm. Residual thermal strain caused by the manufacturing process of silicon carbide molded bodies such as silicon nitride bonded silicon carbide or self-bonded silicon carbide causes microcracks due to sudden temperature changes when used as a protection tube.
This has grown and led to an unstable usage period. The maximum value that a material can withstand against temperature changes is generally expressed by the following equation. ΔT=σf(1-ν)/Eα ΔT=maximum temperature change, σf=average rupture coefficient,
ν: Poisson's ratio, E: Young's modulus, α: coefficient of thermal expansion. Since this value is almost constant depending on the material,
To prevent thermal shock destruction of materials, it is necessary to suppress the difference in internal temperature to below ΔT. For this purpose, it is effective to delay the rate of increase in surface temperature of the material. In the present invention, it has been found that silicon nitride and boron nitride are preferable as materials that are excellent as heat insulating materials and are not corroded by low melting point metals or their antioxidants. It has been found that the effect is further enhanced when this coating layer has two or more layers. It has become clear that this is because when the molten metal permeates into the coating layer, the permeation is suppressed at the interface between the two layers, and the permeation into the internal coating layer is greatly delayed. The coating method is performed by adding an inorganic binder such as aluminum phosphate to silicon nitride or boron nitride powder to make it into a slip, and applying it by spraying or dipping. Further, the thickness of the coating layer is not necessarily sufficient; if it is 3.5 mm or more, the strength of the coating layer itself becomes insufficient and peeling tends to occur. On the other hand, if the thickness is less than 0.3 mm, no heat insulating effect can be expected, so the preferred thickness range is 0.3 to 3.5 mm. Examples of the present invention will be described below. Example 1 A recrystallized silicon carbide protection tube was coated with the following four types of coating layers, and the tube was repeatedly inserted into a holding furnace at 740° C. for Al molten metal and extracted, and its lifespan was measured. (1) No coating layer is applied. (2) Spray coating of silicon nitride on the outer surface. (3) Spray coating the outer surface with boron nitride. (4) Spray coating Al 2 O 3 on the outer surface. In addition, the coating material contains phosphoric acid in each powder.
Al is added as a binding agent, and the film thickness is 1.5 mm in each case. This operation was repeated three times a day with an insertion speed of 30 seconds and a withdrawal speed of 30 seconds into the molten Al, and the service life was investigated and the results were as follows.

【表】 実施例 2 コーテイング層を二層とした以外は実施例1と
同様のものの寿命を調べた。 コーテイング層は一層目は窒化珪素を0.7mm、
二層目は窒化ホウ素を0.7mmとした。その結果、
60〜65日で二層目が剥離した。このものに再度窒
化ホウ素をコーテイングしたところ更に50〜60日
の使用によつて二層目に剥離が見られた。 一般には市販の窒化珪素粉、窒化ホウ素粉には
SiO2、Si、B2O3等の不純物が存在しているが、
これらは反応性に富むものであるため、予め精製
処理を行うことによつてコーテイング剤として更
に耐用性のあるものとすることができる。膜厚に
ついても比較試験を行つたが、例えば窒化ホウ素
を用いた場合0.2mmでは1〜2日で剥離し、又3.6
mmでは1日目でいづれも剥離が見られた。 本発明による保護管は炭化珪素の持つすぐれた
高熱伝導性を生かしてヒーター保護管として耐熱
性があり、且つ熱応答性の良い材料とすることが
できると共にすぐれたコーテイング層を形成する
ことによつて長寿命の保護管とすることができ
た。
[Table] Example 2 The life of a product similar to Example 1 except that the coating layer was two layers was investigated. The first coating layer is silicon nitride with a thickness of 0.7 mm.
The second layer was made of boron nitride with a thickness of 0.7 mm. the result,
The second layer peeled off in 60 to 65 days. When this material was again coated with boron nitride, peeling was observed in the second layer after 50 to 60 days of use. Generally, commercially available silicon nitride powder and boron nitride powder are
Although impurities such as SiO 2 , Si, and B 2 O 3 are present,
Since these are highly reactive, they can be made more durable as coating agents by performing a purification treatment in advance. Comparative tests were also conducted regarding film thickness, and for example, when boron nitride was used, a film of 0.2 mm peeled off in 1 to 2 days, and a film of 3.6 mm
In mm, peeling was observed on the first day. The protection tube according to the present invention takes advantage of the excellent high thermal conductivity of silicon carbide, and can be used as a heater protection tube as a material that is heat resistant and has good thermal responsiveness.It also forms an excellent coating layer. As a result, we were able to create a long-life protection tube.

Claims (1)

【特許請求の範囲】 1 基体が炭化珪素質からなり少なくとも低融点
金属に接触する部分の表面に窒化珪素及び又は窒
化ホウ素よりなる厚さ0.3〜3.5mmのコーテイング
層が設けられていることを特徴とする低融点金属
用浸漬ヒーターの保護管。 2 コーテイング層が二層以上の構造を有してな
る特許請求の範囲第1項記載の低融点金属用浸漬
ヒーターの保護管。
[Scope of Claims] 1. The substrate is made of silicon carbide, and a coating layer of 0.3 to 3.5 mm thick made of silicon nitride and/or boron nitride is provided on at least the surface of the part that contacts the low melting point metal. Protection tube for immersion heaters for low melting point metals. 2. A protective tube for an immersion heater for low melting point metals according to claim 1, wherein the coating layer has a structure of two or more layers.
JP9634081A 1981-06-22 1981-06-22 Protecting tube for low melting point metal dipping heater Granted JPS57210589A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP9634081A JPS57210589A (en) 1981-06-22 1981-06-22 Protecting tube for low melting point metal dipping heater
US06/390,135 US4485143A (en) 1981-06-22 1982-06-18 Silicon carbide material for low-melting point fusion metal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9634081A JPS57210589A (en) 1981-06-22 1981-06-22 Protecting tube for low melting point metal dipping heater

Publications (2)

Publication Number Publication Date
JPS57210589A JPS57210589A (en) 1982-12-24
JPH0131674B2 true JPH0131674B2 (en) 1989-06-27

Family

ID=14162280

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9634081A Granted JPS57210589A (en) 1981-06-22 1981-06-22 Protecting tube for low melting point metal dipping heater

Country Status (1)

Country Link
JP (1) JPS57210589A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5275844U (en) * 1975-11-29 1977-06-06

Also Published As

Publication number Publication date
JPS57210589A (en) 1982-12-24

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