TW201600491A - Process for producing lining structure of vessel for molten metal, and lining structure of vessel for molten metal - Google Patents
Process for producing lining structure of vessel for molten metal, and lining structure of vessel for molten metal Download PDFInfo
- Publication number
- TW201600491A TW201600491A TW104102097A TW104102097A TW201600491A TW 201600491 A TW201600491 A TW 201600491A TW 104102097 A TW104102097 A TW 104102097A TW 104102097 A TW104102097 A TW 104102097A TW 201600491 A TW201600491 A TW 201600491A
- Authority
- TW
- Taiwan
- Prior art keywords
- refractory
- lining
- molten metal
- mass
- metal container
- Prior art date
Links
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 51
- 239000002184 metal Substances 0.000 title claims abstract description 51
- 238000000034 method Methods 0.000 title abstract description 8
- 230000008569 process Effects 0.000 title description 4
- 229910052596 spinel Inorganic materials 0.000 claims abstract description 34
- 239000011029 spinel Substances 0.000 claims abstract description 34
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 24
- 238000010438 heat treatment Methods 0.000 claims abstract description 22
- 239000010459 dolomite Substances 0.000 claims abstract description 8
- 229910000514 dolomite Inorganic materials 0.000 claims abstract description 8
- 239000002689 soil Substances 0.000 claims description 42
- 239000011810 insulating material Substances 0.000 claims description 27
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 24
- 238000010276 construction Methods 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 13
- 229910052742 iron Inorganic materials 0.000 claims description 12
- 239000011823 monolithic refractory Substances 0.000 claims description 5
- 239000011819 refractory material Substances 0.000 claims description 5
- 229910052788 barium Inorganic materials 0.000 claims 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract description 26
- 239000000395 magnesium oxide Substances 0.000 abstract description 13
- 235000012245 magnesium oxide Nutrition 0.000 abstract description 13
- 229910000831 Steel Inorganic materials 0.000 abstract description 4
- 239000010959 steel Substances 0.000 abstract description 4
- 150000002739 metals Chemical class 0.000 abstract 4
- 239000012212 insulator Substances 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 22
- 230000008859 change Effects 0.000 description 18
- 239000000463 material Substances 0.000 description 13
- 230000000694 effects Effects 0.000 description 10
- 229910000420 cerium oxide Inorganic materials 0.000 description 8
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 8
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 6
- 230000007797 corrosion Effects 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 6
- 239000012535 impurity Substances 0.000 description 6
- 239000002994 raw material Substances 0.000 description 5
- 239000002893 slag Substances 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 238000005056 compaction Methods 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000003348 petrochemical agent Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000004901 spalling Methods 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D41/00—Casting melt-holding vessels, e.g. ladles, tundishes, cups or the like
- B22D41/02—Linings
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/10—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on aluminium oxide
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/10—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on aluminium oxide
- C04B35/101—Refractories from grain sized mixtures
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/66—Monolithic refractories or refractory mortars, including those whether or not containing clay
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27D—DETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
- F27D1/00—Casings; Linings; Walls; Roofs
- F27D1/0003—Linings or walls
- F27D1/0006—Linings or walls formed from bricks or layers with a particular composition or specific characteristics
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27D—DETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
- F27D1/00—Casings; Linings; Walls; Roofs
- F27D1/16—Making or repairing linings ; Increasing the durability of linings; Breaking away linings
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3205—Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
- C04B2235/3206—Magnesium oxides or oxide-forming salts thereof
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3205—Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
- C04B2235/3208—Calcium oxide or oxide-forming salts thereof, e.g. lime
- C04B2235/321—Dolomites, i.e. mixed calcium magnesium carbonates
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3217—Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
- C04B2235/3222—Aluminates other than alumino-silicates, e.g. spinel (MgAl2O4)
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/80—Phases present in the sintered or melt-cast ceramic products other than the main phase
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Organic Chemistry (AREA)
- Structural Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Metallurgy (AREA)
- Furnace Housings, Linings, Walls, And Ceilings (AREA)
- Ceramic Products (AREA)
- Casting Support Devices, Ladles, And Melt Control Thereby (AREA)
- Compositions Of Oxide Ceramics (AREA)
Abstract
Description
本發明係關於熔融金屬容器的襯砌構造體(Lining structure)的製造方法及熔融金屬容器的襯砌構造體。 The present invention relates to a method for producing a lining structure of a molten metal container and a lining structure for a molten metal container.
混鐵爐(torpedo car)、高爐(blast furnace 、轉爐(steelmaking converter)、鋼液鍋(molten steel ladle)等之各種熔融金屬容器的襯砌構造體係以在熔融金屬容器的最外側設置鐵皮(outer steel shell),朝熔融金屬容器的內側依序為永久襯砌耐火物、內襯耐火物所構成。位於最內側的內襯耐火物之運行面(working face(of refractory))是與熔融金屬接觸。作為熔融金屬容器之內襯耐火物的特性,被要求對熔融金屬、共存的熔融氧化物之渣(slag)等的耐蝕性(corrosion resistance)、和對伴隨溫度變化所引起之龜裂(spalling)之耐性。 a lining structure system of various molten metal containers such as a torpedo car, a blast furnace, a steelmaking converter, a molten steel ladle, etc., to provide an outer steel on the outermost side of the molten metal container (outer steel) Shell), which is composed of a permanent lining refractory and a lining refractory toward the inside of the molten metal container. The working face (of refractory) of the innermost lining refractory is in contact with the molten metal. The properties of the refractory lining the molten metal container are required to have corrosion resistance to the molten metal, the slag of the coexisting molten oxide, and the like, and the spalling caused by the temperature change. patience.
一般,含有氧化鋁(alumina和苦土(magnesia)之內襯耐火物係藉由在施工後進行燒結,使得 尖晶石化(spinelization)行進。在尖晶石化行進時的體積膨脹,耐火物的體積會膨脹,並且存在於耐火物內的空隙會減少。藉此,可將耐火物緊緻化而使氣孔率降低,能夠防止熔渣侵入到耐火物,因此,能夠減低耐火物的耗損速度。 Generally, a lining refractory containing alumina (magmina) is sintered by post-construction. Spinelization travels. As the volume of the spinel is expanded, the volume of the refractory expands and the voids present in the refractory are reduced. Thereby, the refractory can be made compact, the porosity can be lowered, and the slag can be prevented from intruding into the refractory, so that the refractory wear rate can be reduced.
在熔融金屬容器的使用過程,在內襯耐火物的運行面附近,會產生急遽的溫度上升、下降。因此,如上述般,將在內襯耐火物施工後使氧化鋁與苦土尖晶石化之方法適用於熔融金屬容器的情況時會造成以下這種問題產生。亦即,當內襯耐火物的運行面附近的尖晶石化未充分進行時,因來自於使用過程之熔融金屬的受熱產生溫度上升,因起內襯耐火物產生熱膨脹,因該熱膨脹與伴隨尖晶石化之構造膨脹,會造成在內襯耐火物產生龜裂的問題產生。 In the use of the molten metal container, an imminent temperature rise and fall occurs in the vicinity of the running surface of the lining refractory. Therefore, as described above, the following problem arises when the method of making alumina and bitter soil spinel after the lining of the lining is applied to the molten metal container. That is, when the spinel in the vicinity of the running surface of the lining refractory is not sufficiently performed, the temperature due to the heating of the molten metal from the use process rises due to the thermal expansion of the lining refractory due to the thermal expansion and the accompanying tip. The expansion of the structure of the crystal petrochemical causes a problem of cracking of the lining refractory.
相對於此,在專利文獻1揭示有作為內襯用耐火物,使用以未尖晶石化的氧化鋁與苦土作為主要材料來使用,在內襯用耐火物施工後,以1300℃以上的高溫進行4小時以上的燒成,藉此在熔融金屬容器使用前,使內襯用耐火物尖晶石化。 On the other hand, Patent Document 1 discloses that a refractory for lining is used, and alumina and bitter soil which are not sputtered and petrified are used as main materials, and after refractory construction for the inner lining, the temperature is 1300 ° C or higher. The firing is carried out for 4 hours or more, whereby the lining is sputtered with a refractory before the molten metal container is used.
在專利文獻2提案有添加微量的使熔點降低之二氧化矽(silica),使尖晶石化迅速地進行。 Patent Document 2 proposes to add a small amount of silica which lowers the melting point, and the spinel petrochemical is rapidly carried out.
[專利文獻1]日本特開平10-167846號公報 [Patent Document 1] Japanese Patent Laid-Open No. Hei 10-167846
[專利文獻2]日本專利第4220131號公報 [Patent Document 2] Japanese Patent No. 4220131
但,在專利文獻1所揭示的方法,提案有在熔融金屬容器使用前,使用噴燈將內襯耐火物的運行面以1300℃以上且加熱4小時以上,藉此使內襯耐火物的尖晶石化行進,但,為了以1300℃以上加熱內襯耐火物的運行面,必須採用強力的噴燈設備。又,在內襯耐火物的內部,由於溫度從運行面朝永久襯砌耐火物的方向亦即耐火物的背面方向下降,故,為了進行4小時以上的加熱,讓內襯耐火物的內部充分地尖晶石化,必須需要龐大的能量。因此,適用專利文獻1所揭示的方法並不經濟。 However, in the method disclosed in Patent Document 1, it is proposed to use a burner to heat the running surface of the lining refractory at 1300 ° C or higher and to heat it for 4 hours or more before use of the molten metal container, thereby lining the refractory. Petrochemicals travel, but in order to heat the running surface of the lining refractory at 1300 ° C or above, strong blowtorch equipment must be used. Further, since the temperature inside the refractory is lowered from the running surface toward the direction in which the refractory is permanently lining, that is, in the direction of the back surface of the refractory, the inside of the lining refractory is sufficiently heated for heating for 4 hours or longer. Spinel petrochemicals must require huge amounts of energy. Therefore, the application of the method disclosed in Patent Document 1 is not economical.
在專利文獻2,添加微量的使熔點下降之二氧化矽,使部分產生液相,藉此,對一般的固相擴散,成為迅速的尖晶石化。但,因添加二氧化矽所引起之耐火性能的降低,會有損使耐火物緊緻化而防止熔渣的侵入之尖晶石化的優點,比起不添加二氧化矽而花費充分的時間進行預熱之情況,會有耐火性能較差之問題。 In Patent Document 2, a small amount of cerium oxide having a lowered melting point is added to partially generate a liquid phase, whereby a general solid phase is diffused and rapidly crystallized. However, the reduction in the fire resistance caused by the addition of cerium oxide may impair the advantages of the spinel and petrochemical which make the refractory compact and prevent the intrusion of the slag, and it takes a sufficient time to carry out the addition of cerium oxide. In the case of preheating, there is a problem of poor fire resistance.
本發明係為了解決這樣的問題點而開發完成的發明,其目的在於提供不需要以往這種強力的噴燈設備,即可具有充分的耐火性能之熔融金屬容器之襯砌構造體的製造方法及熔融金屬容器的襯砌構造體。 The present invention has been developed in order to solve such a problem, and an object of the invention is to provide a method for producing a lining structure of a molten metal container which has sufficient fire resistance without requiring a conventional torch device, and a molten metal. The lining structure of the container.
本發明係為了解決這樣的問題點而開發完成的發明,具有以下的特徵。 The present invention has been developed in order to solve such a problem, and has the following features.
[1]一種熔融金屬容器之襯砌構造體的製造方法,係從外側的鐵皮側依序具有永久襯砌耐火物和內襯耐火物的熔融金屬容器之襯砌構造體的製造方法,其特徵為:在前述鐵皮與前述永久襯砌耐火物之間,設置熱傳達係數為100W/m2K以下的隔熱材,施工含有60質量%以上的氧化鋁及4質量%以上的苦土且在1500℃進行3小時的熱處理之前後室溫下的線性變化率為0.8%以上之作為前述內襯耐火物的不燒結耐火物(unfired refractory)及/或不定形耐火物(unshaped refractory),在使用前述熔融金屬容器前,將前述內襯耐火物的運行面預熱。 [1] A method for producing a lining structure of a molten metal container, which is a method for producing a lining structure having a permanent lining refractory and a lining refractory-lined molten metal container from the outer side of the iron sheet, characterized in that: A heat insulating material having a heat transfer coefficient of 100 W/m 2 K or less is provided between the iron sheet and the permanent lining refractory, and the coating contains 60% by mass or more of alumina and 4% by mass or more of bitter soil and is carried out at 1500 ° C. In the case of an unfired refractory and/or an unshaped refractory as the aforementioned lining refractory, the linear change rate at room temperature before and after the heat treatment is 0.8% or more, and the molten metal container is used. Before, the running surface of the aforementioned lining refractory is preheated.
[2]如前述[1]之熔融金屬容器之襯砌構造體的製造方法,其中,進行施工前的前述內襯耐火物係前述苦土的50質量%以上包含方鎂石(periclase)或燒成白雲石(calcined dolomite),在前述熔融金屬容器使用前之預熱,是在施工前的前述內襯耐火物,預熱至方鎂石或燒成白雲石之苦土的一部分氧化鋁與尖晶石化。 [2] The method for producing a lining structure of a molten metal container according to the above [1], wherein the lining refractory before the construction is 50% by mass or more of the bitter soil, comprising pericyl or baking. Calcined dolomite, preheating before the use of the aforementioned molten metal container, is the aforementioned lining refractory before construction, preheating to a portion of alumina and spinel of periclase or burnt dolomite bitter soil Petrochemical.
[3]一種熔融金屬容器的襯砌構造體,其特徵為:藉 由如[1]或[2]所記載之熔融金屬容器之襯砌構造體的製造方法加以製造。 [3] A lining structure of a molten metal container, characterized in that: It is produced by the method for producing a lining structure of a molten metal container as described in [1] or [2].
若依據本發明,能夠提供不需要以往這種強力的噴燈設備,即可具有充分的耐火性能之熔融金屬容器之襯砌構造體的製造方法及熔融金屬容器的襯砌構造體。 According to the present invention, it is possible to provide a method for producing a lining structure of a molten metal container and a lining structure for a molten metal container which have sufficient fire resistance without requiring a conventional torch device.
1‧‧‧鐵皮 1‧‧‧ 铁皮
2‧‧‧隔熱材 2‧‧‧Insulation
3‧‧‧永久襯砌耐火物 3‧‧‧Permanent lining refractory
4‧‧‧內襯耐火物 4‧‧‧ lining refractory
圖1係顯示本發明的實施形態之熔融金屬容器的襯砌構造體的圖。 Fig. 1 is a view showing a lining structure of a molten metal container according to an embodiment of the present invention.
圖2係顯示本發明例1(有隔熱材)與比較例3(無隔熱材)之內襯耐火物從運行面起的距離與苦土的尖晶石化比率之關係的圖。 Fig. 2 is a graph showing the relationship between the distance from the running surface of the lining refractory of Example 1 (with heat insulating material) and Comparative Example 3 (without heat insulating material) and the spinel ratio of bitter soil.
以下,參照圖面,說明關於本發明的實施形態。 Hereinafter, embodiments of the present invention will be described with reference to the drawings.
首先,說明關於本發明的概要。本發明係針對熔融金屬容器的襯砌構造體的製造,發現在內襯耐火物施工後,將能夠讓氧化鋁與苦土尖晶石化的材料作為內襯耐火物使用,並且將隔熱層中介於鐵皮與永久襯砌耐火物之間,藉此,不會使設備費用、能量成本惡化,而能大幅 地減低耐火物成本而開發完成。 First, an outline of the present invention will be described. The invention relates to the manufacture of a lining structure of a molten metal container, and finds that after the lining refractory is constructed, a material capable of allowing alumina and bitter soil spinel to be used as a lining refractory is used, and the heat insulating layer is interposed. Between the iron sheet and the permanent lining refractory, the equipment cost and energy cost will not be deteriorated, and The development was completed by reducing the cost of refractories.
亦即,將苦土的半量以上作為方鎂石(periclase)或燒成白雲石(calcined dolomite)進行調配,為了既可謀求藉由尖晶石化之耐火物的緊緻化,又可減低因內襯耐火物開始使用後急遽的溫度上升時的熱膨脹與伴隨尖晶石化的行進之膨脹的合成膨脹所引起的龜裂,在較內襯耐火物更靠近鐵皮側設置隔熱層。藉此,即可使內襯耐火物的內部之溫度梯度平緩,且可提高內襯耐火物的背面及到背面為止的部位之溫度。其結果,當施工後的預熱時提高進行尖晶石化的比率,進一步使尖晶石化行進至充分深的部分,相對地減低實際開始使用後亦即內襯耐火物開始運行後的尖晶石化之行進的膨脹而可抑制龜裂。藉此,不會使設備費用、能量成本惡化而可大幅地減低耐火物成本。再者,內襯耐火物的背面係指對運行面亦即與熔融金屬接觸的面相反側之面。 That is, more than half of the bitter soil is blended as periclase or calcined dolomite, in order to reduce the refractory by the spinel petrochemical and reduce the internal The crack caused by the rapid expansion of the temperature at which the lining refractory starts to rise and the synthetic expansion accompanying the expansion of the spinel petrochemical is provided with a heat insulating layer closer to the iron side than the lining refractory. Thereby, the temperature gradient inside the lining refractory can be made gentle, and the temperature of the back surface of the lining refractory and the portion to the back surface can be increased. As a result, when the preheating after construction is increased, the ratio of the spinel and petrochemical is increased, and the spinel petrochemical is further advanced to a sufficiently deep portion, and the spinel petrochemical after the actual start of use, that is, after the lining refractory starts to operate, is relatively reduced. The expansion of the travel can suppress cracking. Thereby, the equipment cost and the energy cost are not deteriorated, and the refractory cost can be greatly reduced. Further, the back surface of the lining refractory means the surface opposite to the running surface, that is, the surface in contact with the molten metal.
圖1係顯示本發明的實施形態之熔融金屬容器的襯砌構造體的一例之圖。在熔融金屬容器的最外側設有鐵皮1。襯砌構造體係在內側亦即紙面右側,與熔融金屬(未圖示)接觸。此襯砌構造體係從鐵皮1朝內側,亦即朝熔融金屬進入的方向(襯砌方向)依序具備隔熱材2、永久襯砌耐火物3、內襯耐火物4。 Fig. 1 is a view showing an example of a lining structure of a molten metal container according to an embodiment of the present invention. A metal sheet 1 is provided on the outermost side of the molten metal container. The lining structure is in contact with molten metal (not shown) on the inside, that is, on the right side of the paper. The lining structure system is provided with a heat insulating material 2, a permanent lining refractory 3, and a lining refractory 4 in this order from the iron sheet 1 toward the inner side, that is, in the direction in which the molten metal enters (the lining direction).
在隔熱材2設置於永久襯砌耐火物3與鐵皮1之間的前述襯砌構造體,隔熱材2具有100W/m2K以下的熱傳達係數。一般,永久襯砌耐火物3的熱傳達係數為 100W/m2K左右。在此,熱傳達係數係指針對內襯耐火物4、永久襯砌耐火物3、隔熱材2等的各耐火物層,各層的厚度除各熱傳導率後的值。 The heat insulating material 2 is provided in the lining structure between the permanent lining refractory 3 and the iron sheet 1, and the heat insulating material 2 has a heat transfer coefficient of 100 W/m 2 K or less. Generally, the permanent lining refractory 3 has a heat transfer coefficient of about 100 W/m 2 K. Here, the heat transfer coefficient refers to each refractory layer such as the lining refractory 4, the permanent lining refractory 3, and the heat insulating material 2, and the thickness of each layer is divided by the values of the respective thermal conductivities.
藉由將隔熱材2作為具有較永久襯砌耐火物3低的100W/m2K以下的熱傳達係數之隔熱材所構成,能夠使內襯耐火物4的內部之溫度梯度平緩,並且能增高背面及至背面為止的溫度,能利用使用前的預熱,讓內襯耐火物4的尖晶石化充分地進行。隔熱材2一般為多孔質且耐火性能低,因此,為了將隔熱材2的溫度保持成較低,而將其設在鐵皮1與永久襯砌耐火物3之間。 By forming the heat insulating material 2 as a heat insulating material having a heat transfer coefficient of 100 W/m 2 K or less which is lower than the permanent lining refractory 3, the temperature gradient inside the lining refractory 4 can be made gentle and can be By increasing the temperature of the back surface and the back surface, it is possible to sufficiently perform the spinelization of the lining refractory 4 by the preheating before use. The heat insulating material 2 is generally porous and has low fire resistance. Therefore, in order to keep the temperature of the heat insulating material 2 low, it is provided between the iron sheet 1 and the permanent lining refractory 3.
在此,廉價的隔熱材之熱傳導率大約為0.3W/mK。當將這樣的隔熱材適用作為隔熱材2,而施工厚度作為3mm時,熱傳達係數會成為100W/m2K。例如,藉由將施工厚度作成為2倍的6mm、且熱傳達係數降至50W/m2K或稍微高價但熱傳導率大約為之0.03W/mK的奈米多孔系隔熱材,能夠將熱傳達係數降至10W/m2K,則可使本發明的效果進一步變大。 Here, the thermal conductivity of the inexpensive heat insulating material is about 0.3 W/mK. When such a heat insulating material is applied as the heat insulating material 2, and the construction thickness is 3 mm, the heat transfer coefficient becomes 100 W/m 2 K. For example, a nanoporous heat insulating material having a construction thickness of 6 mm and a heat transfer coefficient of 50 W/m 2 K or a slightly high heat conductivity of about 0.03 W/mK can be used. When the transmission coefficient is lowered to 10 W/m 2 K, the effect of the present invention can be further increased.
永久襯砌耐火物3一般是由鋁氧質等的磚所構成,以砂漿掩埋接縫。永久襯砌耐火物3的熱傳達係數為100W/m2K左右。在圖1中,圖示為1層,但永久襯砌耐火物3亦可設置為2層。 The permanent lining refractory 3 is generally composed of a brick such as alumina or the like, and the joint is buried with mortar. The heat transfer coefficient of the permanent lining refractory 3 is about 100 W/m 2 K. In Fig. 1, one layer is illustrated, but the permanent lining refractory 3 may also be provided in two layers.
內襯耐火物4為含有氧化鋁與苦土,藉由在耐火物施工後進行燒結,使得氧化鋁與苦土尖晶石化之不燒結耐火物及/或不定形耐火物。再者,「不燒結耐火 物」係指成形後施工前未預先燒成之耐火物,「不定形耐火物」係指施工前未預先成形之耐火物。內襯耐火物4係藉由含有60質量%以上的氧化鋁、4質量%以上的苦土之不燒結耐火物及不定形耐火物中的其中一方或雙方所構成為佳。更理想為除了因應特殊用途調配石墨等之情況,期望內襯耐火物4含有80質量%以上的氧化鋁、5質量%以上的苦土。 The lining refractory 4 is an unsintered refractory and/or an amorphous refractory containing alumina and bitter soil, which are sintered by refractory construction to make alumina and bitter spinel. Furthermore, "non-sintering fire resistance "Material" means a refractory that has not been previously fired before construction, and "unshaped refractory" means a refractory that has not been previously formed before construction. It is preferable that the lining refractory 4 is composed of one or both of a non-sintered refractory containing 60% by mass or more of alumina, 4% by mass or more of bitter soil, and an amorphous refractory. More preferably, the lining refractory 4 is required to contain 80% by mass or more of alumina and 5% by mass or more of bitter soil in addition to the case where graphite or the like is blended for a specific use.
又,在使氧化鋁與苦土進行尖晶石化前之內襯耐火物4,50質量%以上的苦土作為方鎂石或燒成白雲石含於耐火物。藉此,因在施工後可提高尖晶石化的比率,所以能夠獲得使內襯耐火物4緊緻化或而提升耐蝕性之效果。在此,雖依據原料價格的市場情況,但期望苦土的90質量%以上作為方鎂石被供給為更理想。 Further, 4,50% by mass or more of the lining refractory before the spinel and the bitter soil are subjected to spinel and petrochemical is contained in the refractory as periclase or calcined dolomite. Thereby, since the ratio of the spinel and petrochemical can be increased after the application, the effect of tightening the lining refractory 4 or improving the corrosion resistance can be obtained. Here, it is preferable that 90% by mass or more of the bitter soil is supplied as the periclase, depending on the market situation of the raw material price.
構成內襯耐火物4的不燒結耐火物及/或不定形耐火物調整成將在1500℃下進行3小時的熱處理前後之室溫的線性變化率(以下亦稱為1500℃的熱處理後之線性變化率)作成為0.8%以上。藉由將1500℃的熱處理後之線性變化率作成為0.8%以上,作成為包含前述隔熱材2的襯砌構造體之情況,在耐火物施工後的預熱時及作為熔融金屬容器使用後(進行運行後),藉由氧化鋁與苦土之尖晶石化,獲得使內襯耐火物4緊緻化而提升耐蝕性之效果。在此,將熱處理溫度設為1500℃、熱處理時間設為3小時之理由為考量作為熔融金屬容器,使用後(進行運行後)的內襯耐火物4之運行面側的溫度履歷,作為藉由尖 晶石化之內襯耐火物4的緊緻化的指標之故。 The non-sintered refractory and/or the monolithic refractory constituting the lining refractory 4 are adjusted to have a linear change rate of room temperature before and after heat treatment at 1500 ° C for 3 hours (hereinafter also referred to as linearity after heat treatment at 1500 ° C). The rate of change is made 0.8% or more. By setting the linear change rate after the heat treatment at 1500 ° C to 0.8% or more, the lining structure including the heat insulating material 2 is used, and during the preheating after the refractory construction and after being used as the molten metal container ( After the operation, the effect of improving the corrosion resistance of the lining refractory 4 is obtained by the spinel of the alumina and the bitter soil. Here, the reason why the heat treatment temperature is 1500 ° C and the heat treatment time is 3 hours is considered as the temperature history of the molten metal container, and the temperature history of the running surface side of the lining refractory 4 after use (after running) tip The reason for the compaction of the refractory 4 lining the crystal petrochemical.
又,在1500℃的熱處理後的室溫之線性變化率未滿0.8%時,即使在作為含有隔熱材2的襯砌構造體的情況,也無法充分地獲得將內襯耐火物4緊緻化並提升耐蝕性之效果。另外,在未含有隔熱材2的層之襯砌構造體,當將在1500℃的熱處理後的室溫之線性變化率作成為0.8%以上時,由於施工後的預熱時以低溫進行尖晶石化的比率低,故內襯耐火物4使用(運行)初期,因尖晶石化所引起之膨脹會急遽地行進,因此,會因內襯耐火物4開始使用後的急遽的溫度上升時之熱膨脹與尖晶石化之膨脹的合成膨脹產生龜裂,變得無法充分地獲得藉由尖晶石化之耐火物的緊緻化使耐蝕性提升而延長耐火物的使用壽命之效果。 In addition, when the linear change rate of the room temperature after the heat treatment at 1500 ° C is less than 0.8%, even when the lining structure including the heat insulating material 2 is used, the lining refractory 4 cannot be sufficiently obtained. And improve the effect of corrosion resistance. In addition, when the linear change rate of the room temperature after the heat treatment at 1500 ° C is 0.8% or more in the lining structure of the layer containing the heat insulating material 2, the spin crystal is spun at a low temperature during preheating after the construction. Since the ratio of the petrochemical is low, the expansion of the lining refractory 4 at the initial stage of operation (operation) causes the expansion due to the spinel petrification to proceed violently. Therefore, the thermal expansion of the lining refractory 4 after the initial temperature rise is started. The expansion of the expansion with the spinel petrification causes cracking, and the effect of increasing the corrosion resistance and prolonging the service life of the refractory by the tightening of the refractory by the spinel is not sufficiently obtained.
且,為了將內襯耐火物4緊緻化而使耐蝕性提升,更期望將在1500℃的熱處理後的室溫之線性變化率作成為1.5%以上。在此,1500℃的熱處理後的線性變化率係分別對應於正值為膨脹、負值為收縮,藉由使作為方鎂石或燒成白雲石而含於耐火物之耐火物的苦土之含有量增加之類的方法而能夠增加,又作為雜質等含於耐火物中的氧化鈦、氧化鐵、二氧化矽之含有量增加等的方法來予以減少的方式進行調整。 Further, in order to improve the corrosion resistance by tightening the lining refractory 4, it is more desirable to set the linear change rate at room temperature after heat treatment at 1500 ° C to 1.5% or more. Here, the linear change rate after the heat treatment at 1500 ° C corresponds to a positive value of expansion and a negative value, respectively, and is made of bitter soil which is contained in the refractory of the refractory material as periclite or fired dolomite. The method of increasing the content can be increased, and it can be adjusted so as to reduce the amount of titanium oxide, iron oxide, and cerium oxide contained in the refractory, such as impurities.
再者,作為供給至熔融金屬容器的內襯耐火物4之耐火物,藉由作成為包含60質量%的氧化鋁、4質量%以上的苦土之材質,可充分地發揮藉由尖晶石化之耐 蝕性提升的效果。 In addition, the refractory of the lining refractory 4 supplied to the molten metal container can be sufficiently made to be lysed by spinel by using a material containing 60% by mass of alumina and 4% by mass or more of bitter soil. Resistance The effect of erosion improvement.
在以上所述的襯砌構造體中,在將隔熱材2中介於鐵皮1與永久襯砌耐火物3之間的情況,促進內襯耐火物4的尖晶石化之效果,可在熔融金屬容器使用前的內襯耐火物4之乾燥、預熱製程產生。 In the lining structure described above, in the case where the heat insulating material 2 is interposed between the iron sheet 1 and the permanent lining refractory 3, the effect of the spinel lining of the lining refractory 4 is promoted, and it can be used in a molten metal container. The drying and preheating process of the front lining refractory 4 is produced.
在以往,當內襯耐火物4乾燥、預熱時,若將內襯耐火物4的運行面的溫度保持在1300℃以上且4小時以上,則內襯耐火物4的尖晶石化不會行進。相對於此,在本發明,於內襯耐火物4的背面側,藉由設置熱傳達係數為100W/m2K以下的隔熱材2,將內襯耐火物4的運行面之溫度提升至800℃,則能夠使運行面附近的內襯耐火物4之尖晶石化充分地行進。再者,從縮短乾燥、預熱時間的點來看,更期望在乾燥、預熱製程末期的內襯耐火物之表面(運行面)溫度為900至1200℃。 In the past, when the lining refractory 4 was dried and preheated, if the temperature of the running surface of the lining refractory 4 was maintained at 1300 ° C or more and 4 hours or more, the spinel lining of the lining refractory 4 did not travel. . On the other hand, in the present invention, the temperature of the running surface of the lining refractory 4 is raised to the back side of the lining refractory 4 by providing the heat insulating material 2 having a heat transfer coefficient of 100 W/m 2 K or less. At 800 ° C, the spinel lining of the lining refractory 4 near the running surface can be sufficiently advanced. Further, from the viewpoint of shortening the drying and preheating time, it is more desirable that the temperature of the surface (running surface) of the lining lining at the end of the drying and preheating process is 900 to 1200 °C.
因此,能夠能有效地抑制因來自於熔融金屬容器開始使用後的熔融金屬之受熱所引起的急遽的溫度上升所引起的龜裂。並且,藉此,不會使設備費用、能量成本惡化而可大幅地減低耐火物成本。又,由於不需要如以往添加二氧化矽,故可維持耐火性能。 Therefore, it is possible to effectively suppress the crack caused by the rapid temperature rise caused by the heat of the molten metal from the start of use of the molten metal container. In addition, the cost of the refractory can be greatly reduced without deteriorating the equipment cost and the energy cost. Further, since it is not necessary to add cerium oxide as in the prior art, the fire resistance can be maintained.
其次,說明關於本發明的實施例。使用圖1所示的襯砌構造體,調查本發明效果。再者,將進行調查的以往例、比較例1至5、本發明例1顯示於表1。在本 發明例1,包含方鎂石以外的苦土之所有的成分為不燒結耐火物及/或不定形耐火物。 Next, an embodiment relating to the present invention will be described. The effect of the present invention was investigated using the lining structure shown in Fig. 1 . In addition, the conventional example which investigated, the comparative examples 1 to 5, and the invention example 1 are shown in Table 1. In this In Inventive Example 1, all components including bitter soil other than periclase are non-sintered refractories and/or monolithic refractories.
(以往例)在襯砌構造體,作為內襯耐火物4,使用91質量%氧化鋁-6質量%苦土,且苦土中的6分之5(質量基準)是預先作為氧化鋁-苦土尖晶石加以調配之1500℃的熱處理後的室溫之線性變化率為0.1%的材質之流入型不定形耐火物。在以往例,未施工有隔熱薄片2。永久襯砌耐火物3的熱傳達係數為100W/m2K。使用壽命為225爐次。 (Conventional Example) In the lining structure, 91% by mass of alumina-6 mass% bitter soil is used as the lining refractory 4, and 5/6 of the bitter soil (mass basis) is previously used as alumina-bitter soil An inflow-type monolithic refractory of a material having a linear change rate of room temperature of 1500 ° C after the heat treatment at 1500 ° C. In the conventional example, the heat insulating sheet 2 was not constructed. The permanent lining refractory 3 has a heat transfer coefficient of 100 W/m 2 K. The service life is 225 heats.
(比較例1)在圖1所示的襯砌構造體,作為內襯耐火物4,使用與以往例相同的91質量%氧化鋁-6質量%苦土,且苦土中的6分之5(質量基準)是預先作為氧化鋁-苦土尖晶石加以調配之1500℃的熱處理後的室溫之線性變化率為0.1%的材質之流入型不定形耐火物。在鐵皮1與永久襯砌耐火物3之間施工有熱傳導率為0.2W/mK且厚度為3mm之隔熱薄片2。隔熱薄片2與永久襯砌耐火物3的總合熱傳達係數為40W/m2K。其結果,比起以往例,使用壽命惡化20%。 (Comparative Example 1) In the lining structure shown in Fig. 1, as the lining refractory 4, 91% by mass of alumina-6 mass% bitter soil similar to the conventional example was used, and 5/6 of the bitter soil was used ( The mass standard) is an inflow type amorphous refractory of a material having a linear change rate of room temperature of 0.1% after heat treatment at 1500 ° C, which is prepared in advance as alumina-bitrite spinel. An insulating sheet 2 having a thermal conductivity of 0.2 W/mK and a thickness of 3 mm was applied between the iron sheet 1 and the permanent lining refractory 3 . The total heat transfer coefficient of the heat insulating sheet 2 and the permanent lining refractory 3 is 40 W/m 2 K. As a result, the service life is deteriorated by 20% compared to the conventional example.
回收使用後的耐火物並進行調查時,熔渣成分之氧化鈣、二氧化矽等對耐火物中之浸潤深度,對於一般的30mm,變成較深的40mm,且在其邊界部亦產生龜裂。一般,在耐火物的背面側實施隔熱時,由於耐火物的溫度會上升而造成耐用度惡化,即使在氧化鋁-苦土系的材質也成為相同結果。 When the refractory after use is recovered and investigated, the depth of penetration of the slag component such as calcium oxide or cerium oxide into the refractory is 40 mm deep for a normal 30 mm, and cracks are also formed at the boundary portion. . In general, when heat is applied to the back side of the refractory, the temperature of the refractory material rises and the durability is deteriorated, and the material of the alumina-bitter soil system has the same result.
(比較例2)其次,作為內襯耐火物4,使用91質量%氧化鋁-6質量%苦土,且苦土中的6分之4(質 量基準)是預先作為氧化鋁-苦土尖晶石加以調配之1500℃的熱處理後的線性變化率為0.3%的材質之流入型不定形耐火物。實施與比較例1相同的隔熱。其結果,浸潤深度減低至30mm前後,但內襯耐火物4的壽命為與以往例相同程度、或較差程度等。 (Comparative Example 2) Next, as the lining refractory 4, 91% by mass of alumina-6 mass% bitter soil was used, and 4/4 of the bitter soil was used. The amount of the standard is an inflow type amorphous refractory of a material having a linear change rate of 0.3% after heat treatment at 1500 ° C which is prepared in advance as alumina-bitrite spinel. The same heat insulation as in Comparative Example 1 was carried out. As a result, the infiltration depth was reduced to about 30 mm, but the life of the lining refractory 4 was the same as or worse than the conventional example.
(比較例3)且,作為內襯耐火物4,使用91質量%氧化鋁-6質量%苦土,且苦土中的95質量%以上作為方鎂石加以調配之1500℃的熱處理後的線性變化率為1.5%的材質之流入型不定形耐火物。再者,在此比較例3,未實工有隔熱薄片。其結果,內襯耐火物4的壽命比起以往例,變長大約11%。 (Comparative Example 3), as the lining refractory 4, 91% by mass of alumina - 6% by mass of bitter soil, and 95% by mass or more of bitter soil, which is formulated as a magnesite, is linear after heat treatment at 1500 ° C. An inflow type amorphous refractory of a material having a rate of change of 1.5%. Further, in Comparative Example 3, there was no actual heat insulating sheet. As a result, the life of the lining refractory 4 is about 11% longer than that of the conventional example.
(比較例4)作為內襯耐火物4,使用94質量%氧化鋁-3質量%苦土,且苦土中的95質量%以上作為方鎂石加以調配的材質之流入型不定形耐火物,施工與比較例1相同的隔熱薄片。其結果,內襯耐火物4的壽命比起以往例變長,但較比較例3變短。這是因為即使使用方鎂石比率高的苦土,在苦土總量未滿4質量%時,1500℃的熱處理後的室溫之線性變化率為較低的0.7%,無法獲得耐火物之緊緻化效果之故。 (Comparative Example 4) As the lining refractory 4, an inflow type monolithic refractory made of 94% by mass of alumina-3 mass% bitter soil and 95% by mass or more of bitter clay as a material for blending with periclase is used. The same heat insulating sheet as in Comparative Example 1 was constructed. As a result, the life of the lining refractory 4 was longer than that of the conventional example, but it was shorter than that of the comparative example 3. This is because even if a bitter soil having a high ratio of periclase is used, when the total amount of bitter soil is less than 4% by mass, the linear change rate of room temperature after heat treatment at 1500 ° C is 0.7% lower, and refractory cannot be obtained. The effect of compaction.
(比較例5)作為內襯耐火物4,使用採用雜質稍多的氧化鋁原料、且90質量%氧化鋁-6質量%苦土且苦土中的95質量%以上作為方鎂石加以調配,並且來自於氧化鋁原料之雜質(氧化鈦、氧化鐵、二氧化矽)為1質量%之1500℃的熱處理後的線性變化率為0.7%之材質的流入 型不定形耐火物,並施工與比較例1相同的隔熱薄片。其結果,內襯耐火物4的壽命比起以往例變長,但較比較例3變短。這是因為即使使用方鎂石比率高的苦土,因容易產生低熔點的液相之雜質的影響,在1500℃的熱處理後的室溫之線性變化率為較低的0.7%,無法獲得耐火物之緊緻化效果之故。 (Comparative Example 5) As the lining refractory 4, an alumina raw material having a slightly larger amount of impurities and 90% by mass of alumina-6 mass% bitter soil and 95% by mass or more of bitter soil were used as the periclite. Inflow of a material having a linear change rate of 0.7% after heat treatment at 1500 ° C in which the impurities (titanium oxide, iron oxide, and cerium oxide) of the alumina raw material are 1% by mass The amorphous refractory was molded, and the same heat insulating sheet as in Comparative Example 1 was applied. As a result, the life of the lining refractory 4 was longer than that of the conventional example, but it was shorter than that of the comparative example 3. This is because even if a bitter soil having a high ratio of periclase is used, the linear change rate at room temperature after heat treatment at 1500 ° C is 0.7% lower due to the influence of impurities which are likely to cause a low melting point liquid phase, and fire resistance cannot be obtained. The effect of the compaction of the object.
再者,在其他的比較例、以往例及本發明例1所使用的內襯耐火物4,來自於氧化鋁原料之雜質(氧化鈦、氧化鐵、二氧化矽)為0.5質量%,在表1所示的任何一個實驗例,作為組成所顯示的數值之總和以外的殘餘部為來自於苦土原料及礬土水泥之氧化鋁及苦土以外的雜質等的成分。 Further, in the other comparative examples, the conventional examples, and the lining refractory 4 used in the first embodiment of the present invention, the impurities (titanium oxide, iron oxide, and cerium oxide) derived from the alumina raw material were 0.5% by mass. In any of the experimental examples shown in Fig. 1, the residual portion other than the sum of the numerical values shown by the composition is a component derived from the alumina of the bitter soil raw material and the alumina cement, and impurities other than the bitter soil.
(本發明例1)作為內襯耐火物4,使用與比較例3相同的91質量%氧化鋁-6質量%苦土,且苦土中的95質量%以上作為方鎂石加以調配之1500℃的熱處理後的室溫之線性變化率為1.5%的材質。又,施工有與比較例1相同的隔熱薄片。其結果,內襯耐火物4的壽命比起以往例,變長大約33%。 (Inventive Example 1) As the lining refractory 4, 91% by mass of alumina-6 mass% bitter soil similar to that of Comparative Example 3 was used, and 95% by mass or more of bitter soil was blended as ferrargsite at 1500 °C. The material has a linear rate of change of room temperature of 1.5% after heat treatment. Further, the same heat insulating sheet as in Comparative Example 1 was applied. As a result, the life of the lining refractory 4 is about 33% longer than that of the conventional example.
亦即,這是因為藉由內襯耐火物4之材質變更的壽命延長中,比較例3的壽命延長為11%,並且藉由設置隔熱材2的層之壽命延長中,本發明例1與比較例3的壽命延長之差異為22%。 That is, this is because the life of Comparative Example 3 is extended by 11% due to the change in the life of the material of the lining refractory 4, and the life of the layer of the heat insulating material 2 is extended, and the present invention is invented. The difference from the life extension of Comparative Example 3 was 22%.
在本發明例1與比較例3之襯砌構造體,在使用前的預熱末期,將內襯耐火物4的運行面的溫度設為 1200℃,將預熱48小時後的內襯耐火物4之尖晶石化比率顯示於圖2。圖2係顯示本發明例1(有隔熱材)與比較例3(無隔熱材)之內襯耐火物從運行面起的距離與苦土的尖晶石化比率之關係的圖。內襯耐火物4的厚度為130mm。 In the lining structures of Inventive Example 1 and Comparative Example 3, the temperature of the running surface of the lining refractory 4 was set at the end of preheating before use. The spinel ratio of the lining refractory 4 after preheating for 48 hours at 1200 ° C is shown in Fig. 2 . Fig. 2 is a graph showing the relationship between the distance from the running surface of the lining refractory of Example 1 (with heat insulating material) and Comparative Example 3 (without heat insulating material) and the spinel ratio of bitter soil. The thickness of the lining refractory 4 is 130 mm.
對於不具有隔熱材2之比較例3,在具有隔熱材2之本發明例1,在各部尖晶石化比率高出24至30點,特別是在中央部之56至75mm的深度之部分,相對於11%是高達35%,對於比較例3,換算成比率則為3.2倍之尖晶石化比率。 In Comparative Example 3 which does not have the heat insulating material 2, in the inventive example 1 having the heat insulating material 2, the spinel ratio in each portion is 24 to 30 points higher, particularly in the depth portion of 56 to 75 mm in the center portion. It is as high as 35% with respect to 11%, and the ratio of spinel to petrochemical ratio is 3.2 times for Comparative Example 3.
藉此可得知,對含有60質量%以上的氧化鋁、4質量%以上的苦土且苦土的50質量%以上是作為方鎂石被供給之內襯耐火物4,藉由在鐵皮1與永久襯砌耐火物3之間設置熱傳達係數為100W/m2K以下的隔熱材,能夠延長內襯耐火物4的耐用時間。 In this way, it is found that 60% by mass or more of the alumina and 4% by mass or more of the bitter soil and 50% by mass or more of the bitter soil are the lining refractory 4 supplied as the periclase by the iron sheet 1 A heat insulating material having a heat transfer coefficient of 100 W/m 2 K or less is provided between the permanent lining refractory 3 and the durability of the lining refractory 4 can be prolonged.
再者,本發明不限於前述實施形態,當然能夠適用各種設計變更。 Furthermore, the present invention is not limited to the above embodiment, and of course, various design changes can be applied.
1‧‧‧鐵皮 1‧‧‧ 铁皮
2‧‧‧隔熱材 2‧‧‧Insulation
3‧‧‧永久襯砌耐火物 3‧‧‧Permanent lining refractory
4‧‧‧內襯耐火物 4‧‧‧ lining refractory
Claims (3)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2014010237 | 2014-01-23 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW201600491A true TW201600491A (en) | 2016-01-01 |
| TWI572581B TWI572581B (en) | 2017-03-01 |
Family
ID=53681206
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW104102097A TWI572581B (en) | 2014-01-23 | 2015-01-22 | A method for manufacturing a lining structure of a molten metal container, and a lining structure of a molten metal container |
Country Status (5)
| Country | Link |
|---|---|
| JP (1) | JP5907312B2 (en) |
| KR (1) | KR101929640B1 (en) |
| CN (1) | CN105917186B (en) |
| TW (1) | TWI572581B (en) |
| WO (1) | WO2015111394A1 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6428692B2 (en) * | 2016-03-28 | 2018-11-28 | Jfeスチール株式会社 | Refractory structure |
| TWI837098B (en) | 2017-08-29 | 2024-04-01 | 美商維蘇威美國公司 | Refractory lining structure and metallurgical vessel |
| JP6995709B2 (en) * | 2018-07-06 | 2022-01-17 | 新東工業株式会社 | Cast steel casting manufacturing system |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04220131A (en) | 1991-01-28 | 1992-08-11 | Mitsubishi Materials Corp | Manufacture of deformed section bar |
| JP3192806B2 (en) * | 1993-02-01 | 2001-07-30 | 品川白煉瓦株式会社 | Heating and drying method for refractory lining of closed vessel for molten steel treatment |
| JPH07330452A (en) * | 1994-06-13 | 1995-12-19 | Harima Ceramic Co Ltd | Cast refractories for molten steel processing equipment |
| JPH10167846A (en) | 1996-12-02 | 1998-06-23 | Kobe Steel Ltd | Drying method for alumina-magnesia amorphous refractory material and amorphous refractory material produced by that method |
| JP2001302364A (en) * | 2000-04-20 | 2001-10-31 | Nippon Steel Corp | Zirconium oxide-containing alumina-magnesia castable refractories and molten metal containers for metal refining |
| JP2002037677A (en) * | 2000-05-16 | 2002-02-06 | Nippon Steel Corp | Precast block drying method |
| JP4220131B2 (en) * | 2001-02-01 | 2009-02-04 | 品川白煉瓦株式会社 | Amorphous refractory composition for ladle |
| JP2003171183A (en) * | 2001-12-05 | 2003-06-17 | Nippon Steel Corp | Low modulus alumina-magnesia castable refractories, precast blocks and molten metal containers |
| JP3726778B2 (en) * | 2002-06-05 | 2005-12-14 | Jfeスチール株式会社 | Hot metal holding container |
| JP2004142957A (en) * | 2002-10-21 | 2004-05-20 | Nippon Steel Corp | Low modulus alumina-magnesia castable refractories, precast blocks and molten metal containers |
| JP4692104B2 (en) * | 2004-06-29 | 2011-06-01 | Jfeスチール株式会社 | Indefinite refractory |
| JP3903321B2 (en) * | 2004-12-28 | 2007-04-11 | 株式会社大紀アルミニウム工業所 | Molten metal ladle |
| JP5366560B2 (en) * | 2009-01-05 | 2013-12-11 | 日新製鋼株式会社 | Non-fired brick refractory |
| JP5659462B2 (en) * | 2009-05-14 | 2015-01-28 | Jfeスチール株式会社 | Refractory lining structure for steelmaking containers |
| JP5680297B2 (en) * | 2009-11-17 | 2015-03-04 | Jfeスチール株式会社 | Refractory lining structure for steelmaking containers |
| JP5601290B2 (en) * | 2011-08-17 | 2014-10-08 | 新日鐵住金株式会社 | Lining repair method |
| JP5741316B2 (en) * | 2011-08-17 | 2015-07-01 | 新日鐵住金株式会社 | Lining drying method |
| CN103172388A (en) * | 2011-12-20 | 2013-06-26 | 旭硝子陶瓷株式会社 | Magnesium spinel lithoidal refractory body |
-
2015
- 2015-01-16 CN CN201580004938.3A patent/CN105917186B/en active Active
- 2015-01-16 KR KR1020167022832A patent/KR101929640B1/en active Active
- 2015-01-16 WO PCT/JP2015/000185 patent/WO2015111394A1/en not_active Ceased
- 2015-01-16 JP JP2015517516A patent/JP5907312B2/en active Active
- 2015-01-22 TW TW104102097A patent/TWI572581B/en active
Also Published As
| Publication number | Publication date |
|---|---|
| CN105917186B (en) | 2017-11-28 |
| TWI572581B (en) | 2017-03-01 |
| CN105917186A (en) | 2016-08-31 |
| JPWO2015111394A1 (en) | 2017-03-23 |
| KR101929640B1 (en) | 2018-12-14 |
| KR20160111484A (en) | 2016-09-26 |
| JP5907312B2 (en) | 2016-04-26 |
| WO2015111394A1 (en) | 2015-07-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN104591752B (en) | Burnt magnesia spinel brick for RH refining furnace dip pipe and circulating pipe and preparation method thereof | |
| KR100938727B1 (en) | Refractory wall and refractory bricks for building said wall | |
| TWI572581B (en) | A method for manufacturing a lining structure of a molten metal container, and a lining structure of a molten metal container | |
| JP5361795B2 (en) | Lined casting material | |
| US1458724A (en) | Refractory composition | |
| CN103936443A (en) | Novel micropore corundum brick and preparation method thereof | |
| JP3679443B2 (en) | Unstructured refractory lining structure for chaotic cars | |
| JP6287918B2 (en) | Manufacturing method of container for high temperature | |
| JP2015189640A (en) | Alumina-silicon carbide-carbon brick | |
| JP6742579B2 (en) | How to build a molten metal container | |
| TW201326081A (en) | Ramming mass for the refractory lining of a metallurgical vessel, method for the placement thereof and metallurgical vessel, in particular blast furnace, comprising a lining using said ramming mass | |
| JP2951432B2 (en) | Unfired refractory containing magnesia | |
| JP3238592B2 (en) | Irregular cast refractory moldings | |
| JP7802608B2 (en) | Refractory structure of ladle and operation method using ladle with said refractory structure | |
| JPH0725669A (en) | Castable refractory for lining of sintered-metal container | |
| CN217083308U (en) | Composite magnesia-chrome brick | |
| JP2003002754A (en) | Heat insulating castable refractory | |
| JPH046150A (en) | Magnesia-chrome refractories | |
| JPS5855379A (en) | Refractory castable for ladle lining | |
| JPH0671422A (en) | How to line the ladle floor | |
| JPH06199575A (en) | Alumina-spinel castable refractory | |
| JPH08290958A (en) | Oxide refractory and method for manufacturing the same | |
| JP2013231592A (en) | Construction method of monolithic refractory | |
| JPH0375275A (en) | Magnesian refractory mortar | |
| JPH06172020A (en) | Refractory material containing magnesia component |