KR20110076702A - Binder composition for carbon based refractory, carbon based refractory composition, carbon based refractory and method for producing the same - Google Patents
Binder composition for carbon based refractory, carbon based refractory composition, carbon based refractory and method for producing the same Download PDFInfo
- Publication number
- KR20110076702A KR20110076702A KR1020090133462A KR20090133462A KR20110076702A KR 20110076702 A KR20110076702 A KR 20110076702A KR 1020090133462 A KR1020090133462 A KR 1020090133462A KR 20090133462 A KR20090133462 A KR 20090133462A KR 20110076702 A KR20110076702 A KR 20110076702A
- Authority
- KR
- South Korea
- Prior art keywords
- carbon
- based refractory
- binder
- titanium
- composition
- Prior art date
Links
Classifications
-
- 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
-
- 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
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/52—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbon, e.g. graphite
- C04B35/522—Graphite
-
- 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
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
- C04B35/6303—Inorganic additives
-
- 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
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
- C04B35/632—Organic additives
- C04B35/634—Polymers
- C04B35/63448—Polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C04B35/63452—Polyepoxides
-
- 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
- C04B2235/3231—Refractory metal oxides, their mixed metal oxides, or oxide-forming salts thereof
- C04B2235/3232—Titanium oxides or titanates, e.g. rutile or anatase
-
- 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
- C04B2235/38—Non-oxide ceramic constituents or additives
- C04B2235/3817—Carbides
- C04B2235/3826—Silicon carbides
-
- 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
- C04B2235/38—Non-oxide ceramic constituents or additives
- C04B2235/3817—Carbides
- C04B2235/3839—Refractory metal carbides
- C04B2235/3843—Titanium carbides
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Ceramic Products (AREA)
Abstract
Description
본 발명은 탄소계 내화물용 결합재 조성물, 탄소계 내화물 및 그 제조방법에 관한 것으로, 더욱 상세하게는 성형성이 우수하고, 내열충격성이 현저히 향상된 탄소계 내화물용 결합재 조성물, 탄소계 내화물 및 그 제조방법에 관한 것이다.The present invention relates to a carbon-based refractory binder composition, a carbon-based refractory material and a method for manufacturing the same. More particularly, the binder composition for a carbon-based refractory material, a carbon-based refractory material and a method for producing the same, having excellent moldability and significantly improved thermal shock resistance. It is about.
본 발명은 내화물 조성물에 관한 것으로, 더욱 상세하게는 성형성이 우수하고, 내스폴링성이 현저히 향상된 탄소계 내화물 조성물에 관한 것이다.The present invention relates to a refractory composition, and more particularly, to a carbon-based refractory composition excellent in moldability and remarkably improved spalling resistance.
탄소를 함유하는 탄소계 내화물은 산업 설비에서 고온에 대한 보호를 위해 사용되는 것으로, 내화물의 주 사용영역은 강철, 유리, 시멘트 및 비철 금속 산업이다. Carbon-based refractory containing carbon is used for protection against high temperatures in industrial facilities, the main application of the refractory is the steel, glass, cement and nonferrous metals industry.
이러한 내화물은 일반적으로, 배소 무연탄, 인상흑연 등의 탄소계 골재에 결 합재를 첨가하여 혼련하고, 이를 성형한 후, 소성하여 제조된다.Such refractory materials are generally produced by adding kneaded materials to carbon-based aggregates such as roasted anthracite coal and impression graphite, kneading them, molding them, and then firing them.
이때, 종래에 결합재로는 페놀계 수지, 석탄계 핏치, 또는 석유계 핏치 등이 사용되어 왔으며, 비산화분위기에서 열처리 시 고온특성, 내식성 및 성형성 등을 확보하기 위하여 가능한 많은 양의 잔존탄소를 생성하는 결합재를 사용하여왔다. 그러나, 상기 핏치를 결합재로 사용할 경우, 성형성이 저하된다는 문제점이 있고, 열경화성 수지를 결합재로 사용할 경우는 성형성 확보는 용이한 반면에 열처리에 의해서 비정질 탄소(vitreous carbon, glassy carbon)을 형성하여, 내화물의 취성파괴(brittle catastrophic fracture)를 유도하며 열충격 저항성이 결여된다는 문제점이 있다.In this case, phenolic resins, coal-based pitches, or petroleum-based pitches have been used as binders in the past, and as much residual carbon is produced as possible in order to secure high temperature characteristics, corrosion resistance, and moldability during heat treatment in a non-oxidizing atmosphere. Has been using a binder. However, when the pitch is used as a binder, there is a problem that the moldability is lowered. When using the thermosetting resin as a binder, the moldability is easily secured, but amorphous carbon (vityous glass, glassy carbon) is formed by heat treatment. In addition, there is a problem of inducing brittle catastrophic fracture of the refractory and lacking thermal shock resistance.
본 발명은 성형성이 우수하고, 내스폴링성이 현저히 향상된 탄소계 내화물용 결합재 조성물, 탄소계 내화물 조성물, 탄소계 내화물 및 그 제조방법을 제공하는 것을 목적으로 한다.An object of the present invention is to provide a binder composition for a carbon-based refractory material, a carbon-based refractory composition, a carbon-based refractory material, and a method for producing the same, having excellent moldability and remarkably improved spalling resistance.
본 발명은 상기 과제를 해결하기 위한 수단으로서, 산화티탄 또는 그의 전구체; 및 바인더 수지를 포함하는 탄소계 내화물용 결합재 조성물을 제공한다.The present invention is a means for solving the above problems, titanium oxide or a precursor thereof; And it provides a binder composition for carbon-based refractory comprising a binder resin.
본 발명은 상기 과제를 해결하기 위한 다른 수단으로서, 골재;와The present invention is another means for solving the above problems, aggregate; and
산화티탄 또는 그의 전구체; 및 바인더 수지를 함유하는 탄소계 내화물용 결합재 조성물을 포함하는 탄소계 내화물 조성물을 제공한다.Titanium oxide or a precursor thereof; And it provides a carbon-based refractory composition comprising a binder composition for carbon-based refractory containing a binder resin.
본 발명은 상기 과제를 해결하기 위한 또 다른 수단으로서, 본 발명에 따른 산화티탄 또는 그의 전구체와 바인더 수지를 포함하는 결합재를 제조하는 제 1단계; 상기 1단계에서 제조된 결합재를 골재와 혼합하는 제 2단계; 및 상기 2단계에서 얻어진 혼합물을 성형하고 열처리 하는 제 3단계를 포함하는 탄소계 내화물의 제조방법을 제공한다.The present invention as another means for solving the above problems, the first step of producing a binder comprising a titanium oxide or a precursor thereof and a binder resin according to the present invention; A second step of mixing the binder prepared in step 1 with aggregate; And it provides a method for producing a carbon-based refractory comprising a third step of molding and heat-treating the mixture obtained in the second step.
본 발명은 상기 과제를 해결하기 위한 또 다른 수단으로서, 본 발명의 탄소계 내화물의 제조방법에 따라 제조되고, 티타늄 카바이드(TiC)를 포함하는 탄소계 내화물을 제공한다.As another means for solving the above problems, the present invention provides a carbon-based refractory material prepared according to the method for producing a carbon-based refractory material of the present invention and containing titanium carbide (TiC).
본 발명에서는, 산화티탄 전구체와 바인더 수지로 이루어진 결합재를 사용하여, 내화물 제조시 발생되는 탄소를 촉매흑연화를 통해 비정질 탄소에서 결정질 흑연으로 전환시켜 줌으로써, 성형성은 유지할 수 있고, 내스폴링성과 내산화성을 향상시킬 수 있는 탄소계 내화물용 결합재 조성물, 탄소계 내화물 조성물, 탄소계 내화물 및 그의 제조방법을 제공할 수 있다.In the present invention, by using a binder composed of a titanium oxide precursor and a binder resin, by converting the carbon generated in the production of the refractory from amorphous carbon to crystalline graphite through catalytic graphite, the moldability can be maintained, spalling resistance and oxidation resistance It is possible to provide a binder composition for a carbon-based refractory material, a carbon-based refractory composition, a carbon-based refractory material and a method of manufacturing the same.
본 발명은 산화티탄 또는 그의 전구체; 및 바인더 수지를 포함하는 탄소계 내화물용 결합재 조성물을 제공한다. The present invention is titanium oxide or precursors thereof; And it provides a binder composition for carbon-based refractory comprising a binder resin.
이하, 본 발명을 상세하게 설명한다. EMBODIMENT OF THE INVENTION Hereinafter, this invention is demonstrated in detail.
본 발명에서 사용되는 산화티탄은 그 종류를 특별히 제한하는 것은 아니고, 아나타제 (anatase) 형 및 루틸 (rutile) 형과 같은 결정형은 특히 제한되지 않는다. The titanium oxide used in the present invention is not particularly limited in kind, and the crystalline forms such as the anatase and rutile forms are not particularly limited.
또한, 상기 산화티탄의 형상은 구형, 이방형과 같은 정형의 입자, 및 부(不)정형의 입자를 제한 없이 사용할 수 있다. 상기 산화티탄은 입도가 200 내지 350 메쉬(mesh)의 산화티탄 분체를 사용할 수 있으며, 이러한 산화티탄 분체의 입도가 200 메쉬 미만일 경우에는 미분으로 인해 공정상의 문제점이 있을 수 있으며, 350 메쉬를 초과할 경우에는 균일한 혼합이 어려울 수 있다.In addition, the shape of the titanium oxide can be used without limitation, spherical particles, amorphous particles such as anisotropic particles, and non-crystalline particles. The titanium oxide may use titanium oxide powder having a particle size of 200 to 350 mesh, and when the particle size of the titanium oxide powder is less than 200 mesh, there may be a process problem due to fine powder, and may exceed 350 mesh. In this case, even mixing can be difficult.
상기 산화티탄 전구체는 소성되어 산화티탄으로 전환될 수 있는 것이면 특별히 한정하는 것은 아니나, 예를 들어, 상기 산화티탄 전구체는 티탄함유 금속염, 티타늄알콕사이드, 수산화티탄, 수산화함유티탄, 및 티타늄 할라이드로 이루어진 군 중에서 선택된 하나 이상일 수 있다. 이러한, 상기 산화티탄 또는 그의 전구체는 탄소계 내화물용 결합재에 포함되는 것으로, 결합재 조성물 100중량부 중 0.1 내지 50중량부인 것이 바람직하며, 5 내지 40 중량부인 것이 보다 바람직하며, 10 내지 20 중량부인 것이 가장 바람직하다. 만약, 상기 산화티탄 또는 그의 전구체가 0.1 중량부 미만일 경우, 만족할만한 내열충격성을 갖지 못하게 되고, 50 중량부를 초과할 경우, 결합재의 점도증가로 인해 결합력에 지장을 줄 수 있으며, 지나 친 이산화탄소 발생으로 인해 파괴강도에 영향을 줄 수 있다. The titanium oxide precursor is not particularly limited as long as it can be calcined and converted to titanium oxide. For example, the titanium oxide precursor is a group consisting of titanium-containing metal salts, titanium alkoxides, titanium hydroxides, titanium hydroxide-containing titanium titanium, and titanium halides. It may be one or more selected from. The titanium oxide or its precursor is included in the binder for carbon-based refractory, preferably 0.1 to 50 parts by weight, more preferably 5 to 40 parts by weight, and 10 to 20 parts by weight of the binder composition. Most preferred. If the titanium oxide or its precursor is less than 0.1 parts by weight, it does not have a satisfactory thermal shock resistance, and if it exceeds 50 parts by weight, it may interfere with the binding force due to the increase in viscosity of the binder, excessive carbon dioxide generation This can affect the breaking strength.
본 발명에서, 상기 바인더 수지는 내화물에 사용되는 통상의 바인더 수지를 사용할 수 있으며, 구체적으로, 난흑연화성 탄소를 생성하는 수지를 사용할 수 있다. 이와 같은 난흑연화성 탄소를 생성하는 수지는 예를 들어, 에폭시 수지, 시아네이트 에스테르 수지, 비스말레이미드 수지, 폴리이미드 수지, 벤조시클로부텐계 수지 및 페놀 수지로 이루어진 군으로부터 선택된 하나 이상을 들 수 있다. 이러한, 바인더 수지는 결합재 조성물 100중량부에 대하여, 40 내지 90 중량부로 포함되는 것이 바람직하며, 60 내지 80 중량부인 것이 보다 바람직하다. 10 내지 20 중량부인 것이 가장 바람직하다. 만약, 상기 바인더 수지가 40 중량부 미만일 경우, 저조한 결합력으로 인해 내화물의 강도가 저하될 뿐만 아니라 내화물의 제조시 상온에서의 성형이 불가능하고, 90 중량부를 유동성이 지나치게 증가하여 성형강도가 오히려 감소될 수 있으며, 열처리 중 점도가 낮은 바인더 수지가 외부로 배출되어 내화물 전체의 성능이 열화 될 수 있다는 문제점이 있다.In the present invention, the binder resin may be used a conventional binder resin used in the refractory, specifically, may be used a resin that produces non-graphitizable carbon. Examples of such a non-graphitizable carbon resin include one or more selected from the group consisting of epoxy resins, cyanate ester resins, bismaleimide resins, polyimide resins, benzocyclobutene resins and phenol resins. have. It is preferable that such a binder resin is contained in 40 to 90 weight part with respect to 100 weight part of binder composition, and it is more preferable that it is 60 to 80 weight part. Most preferably, it is 10-20 weight part. If the binder resin is less than 40 parts by weight, the strength of the refractory is not only lowered due to poor bonding strength, but also molding at room temperature is impossible during the production of the refractory, and 90 parts by weight of the fluidity is excessively increased so that the molding strength may be reduced. The binder resin may be discharged to the outside during the heat treatment to deteriorate the performance of the entire refractory.
본 발명은 또한, 골재;와 산화티탄 또는 그의 전구체와 바인더 수지를 함유하는 결합재를 포함하는 탄소계 내화물 조성물에 관한 것이다.The present invention also relates to a carbon-based refractory composition comprising an aggregate; and a binder containing titanium oxide or a precursor thereof and a binder resin.
본 발명에 사용되는 골재는 내화물에 사용되는 통상의 골재를 사용할 수 있으며, 구체적으로 흑연, 카본블랙(carbon black), 무연탄, 페이즈(mesophase) 카 본, Al2O3 클린커(clinker), MgO 클린커, ZrO2 클린커 및 SiO2 클린커로 이루어진 군으로부터 선택된 하나 이상을 단독 또는 혼합하여 사용할 수 있으며, 이러한 골재는 최종 내화물이 사용되는 용도, 목적 등에 따라 선택하여 사용할 수 있다.As the aggregate used in the present invention, a conventional aggregate used for refractory may be used, and specifically, graphite, carbon black, anthracite, mesophase carbon, Al 2 O 3 clinker, MgO One or more selected from the group consisting of a clinker, a ZrO 2 clinker, and a SiO 2 clinker may be used alone or in combination. Such aggregates may be selected and used according to the use, purpose, and the like of the final refractory material.
또한, 상기 산화티탄 또는 그의 전구체와 바인더 수지를 함유하는 결합재는 상술한 본 발명의 탄소계 내화물용 결합재 조성물을 동일하게 사용할 수 있다.In addition, as the binder containing the titanium oxide or its precursor and binder resin, the binder composition for carbon-based refractory materials of the present invention described above can be used in the same manner.
상기 결합재는 골재 100 중량부에 대하여 2 내지 5 중량부로 포함되는 것이 바람직하다. 그 함량이 2 중량부 미만일 경우에는 상온에서의 성형이 불가능하고, 결합능이 미미하고, 5 중량부를 초과할 경우에는 유동성이 지나치게 증가하여 성형강도가 오히려 감소될 수 있으며, 열처리 중 점도가 낮은 바인더 수지가 외부로 배출되어 내화물 전체의 성능이 열화 될 수 있다는 문제점이 있다.The binder is preferably included 2 to 5 parts by weight based on 100 parts by weight of the aggregate. If the content is less than 2 parts by weight, molding at room temperature is impossible, the binding capacity is insignificant, and if the content is more than 5 parts by weight, the fluidity may be excessively increased, thereby reducing the molding strength. There is a problem that is discharged to the outside can degrade the performance of the entire refractory.
한편, 상기 탄소계 내화물 조성물은 산화방지제를 추가로 포함할 수 있다. 이러한 상기 산화방지제는 산화방지제 역할뿐만 아니라, 동시에 결합재의 중/축합 촉매 작용을 한다. 즉, 상기 산화방지제는 결합재의 중/축합 촉매 작용을 하고, 이에 따라 결합재의 중/축합 반응이 활발하게 일어나 골재 성분들을 더욱 견고하게 결합시킬 수 있게 된다. On the other hand, the carbon-based refractory composition may further comprise an antioxidant. Such antioxidants not only act as antioxidants, but also act as poly / condensation catalysts for the binder. That is, the antioxidant acts as a poly / condensation catalyst of the binder, and thus the poly / condensation reaction of the binder is active to more firmly bind the aggregate components.
본 발명에서 사용할 수 있는 산화방지제는 구체적으로, 탄화규소, 질화규소, 티타니아, 지르코니아, 지르콘, 산화 알루미늄, 실리카, 뮬라이트, 2규화 몰리브덴, 탄화 붕소, 및 붕소로 이루어지는 군으로부터 선택된 하나 이상을 사용할 수 있다.Antioxidants that may be used in the present invention may specifically use one or more selected from the group consisting of silicon carbide, silicon nitride, titania, zirconia, zircon, aluminum oxide, silica, mullite, molybdenum silicide, boron carbide, and boron. .
상기 산화방지제는 골재 100 중량부에 대하여 2 내지 5 중량부로 사용되는 것이 바람직하며, 그 함량이 2 중량부 미만이거나 5 중량부를 초과할 경우에는 산화방지제로서의 역할 및 결합재의 중/축합 촉매 작용이 미미하다는 문제점이 있다.The antioxidant is preferably used in an amount of 2 to 5 parts by weight based on 100 parts by weight of aggregate, and when the content thereof is less than 2 parts by weight or more than 5 parts by weight, the role as an antioxidant and the poly / condensation catalysis of the binder are insignificant. There is a problem.
한편, 본 발명은 산화티탄 또는 그의 전구체와 바인더 수지를 포함하는 결합재를 제조하는 제 1단계; 상기 1단계에서 제조된 결합재를 골재와 혼합하는 제 2단계; 및 상기 2단계에서 얻어진 혼합물을 성형하고 열처리 하는 제 3단계를 포함하는 내화물의 제조방법을 제공한다.On the other hand, the present invention comprises a first step of producing a binder comprising titanium oxide or a precursor thereof and a binder resin; A second step of mixing the binder prepared in step 1 with aggregate; And it provides a method for producing a refractory comprising a third step of molding and heat-treating the mixture obtained in the second step.
상기 제 1단계는 상술한 본 발명의 탄소계 내화물용 결합재 조성물을 혼합하여 결합제를 제조하는 단계이다. The first step is to prepare a binder by mixing the binder composition for carbon-based refractory materials of the present invention described above.
상기 제 2단계는 결합재를 골재와 혼합하는 단계이다. 이때, 상기 제 1단계와 2단계의 혼합방법은 통상의 혼합방법을 이용한다.The second step is a step of mixing the binder with the aggregate. At this time, the mixing method of the first step and the second step uses a conventional mixing method.
한편, 상기 제 2단계는 산화방지제를 첨가하여 혼합하는 단계를 추가로 포함할 수 있다. 이러한, 산화방지제는 산화방지제로서의 역할과 결합재의 중/축합 촉매 역할을 한다. On the other hand, the second step may further comprise the step of mixing by adding an antioxidant. These antioxidants serve as antioxidants and as poly / condensation catalysts for the binder.
상기 제 3단계에는 상기 2단계에서 얻어진 혼합물을 성형하고 열처리 하는 것으로, 성형 방법은 목적으로 하는 제품의 형태, 형상에 따라 적당한 방법으로 성형할 수 있고, 열처리 방법은 상기에서 성형된 성형물을 환원 분위기 또는 비산화 분위기 중에서 열처리한다. 이때, 열처리는 800 내지 1800℃의 열처리 온도에서 수 행될 수 있고, 보다 구체적으로는 800 내지 1600℃의 온도에서 수행될 수 있다. 상기 열처리 온도의 범위 내에서 적합한 소성강도를 얻을 수 있다.In the third step, by molding and heat-treating the mixture obtained in the second step, the molding method can be molded in a suitable method according to the shape and shape of the target product, the heat treatment method is a reducing atmosphere of the molded article Or heat treatment in a non-oxidizing atmosphere. At this time, the heat treatment may be performed at a heat treatment temperature of 800 to 1800 ℃, more specifically may be carried out at a temperature of 800 to 1600 ℃. Suitable plastic strength can be obtained within the range of the heat treatment temperature.
상기 제 3단계의 열처리 시간은 특별히 제한되는 것은 아니지만, 예를 들면, 5분 내지 20분 동안 수행될 수 있다.The heat treatment time of the third step is not particularly limited, but may be performed, for example, for 5 minutes to 20 minutes.
또한, 상기 열 처리를 연속로에서 수행함에 따라 생산성을 향상시킬 수도 있다.In addition, productivity may be improved by performing the heat treatment in a continuous furnace.
아울러, 상기 열 처리를 통하여, 본 발명의 결합재에 포함되어 있던 산화티탄의 전구체는 약 300 내지 600℃의 온도에서 소성되어, 산화티탄을 수득할 수 있다. In addition, through the heat treatment, the precursor of titanium oxide contained in the binder of the present invention may be calcined at a temperature of about 300 to 600 ° C. to obtain titanium oxide.
[반응식 1]Scheme 1
TiO2+2C→TiC+CO2 TiO 2 + 2C → TiC + CO 2
이와 같이, 첨가 또는 제조된 산화티탄은 탄소계 내화물의 소성공정 시 상기 반응식 1과 같은 반응을 유도하여, 탄소계 내화물의 소성공정 시 발생하는 비정질 탄소를 촉매흑연화를 통해 결정질 흑연으로 전환시키게 되고, 이로 인해, 탄소계 내화물의 내열충격성을 개선하고, 더 나아가 내산화성을 증진하는 내화물을 제공할 수 있다. As such, the added or prepared titanium oxide induces a reaction as in Scheme 1 during the firing process of the carbon-based refractory, and converts amorphous carbon generated during the firing process of the carbon-based refractory to crystalline graphite through catalytic graphite. Due to this, it is possible to provide a refractory which improves the thermal shock resistance of the carbon-based refractory material and further enhances the oxidation resistance.
따라서, 본 발명의 탄소계 내화물의 제조방법에 따라 제조된 탄소계 내화물은 티타늄 카바이드(TiC)를 포함할 수 있다. Therefore, the carbon-based refractory material prepared according to the method for preparing carbon-based refractory material of the present invention may include titanium carbide (TiC).
또한, 상기 탄소계 내화물은 탄소 입자의 평균 격자면간격(d002)이 0.334nm 내지 0.338nm일 수 있으며, 바람직하게는 0.335㎚ 내지 0.337㎚일 수 있다. 이러한 탄소 입자의 평균 격자면간격(d200)의 범위 내에서 적합한 결정성과 내스폴링성을 유지할 수 있다. In addition, the carbon-based refractory material, the average lattice spacing (d 002 ) of the carbon particles may be 0.334nm to 0.338nm, preferably 0.335nm to 0.337nm. Suitable crystallinity and spalling resistance can be maintained within the range of the average lattice spacing d 200 of such carbon particles.
또한, 상기 반응식 1로 표기되는 화학반응에 의해 생성된 이산화탄소(CO2)는 내화물 외부로 배출된다. 이렇게 배출되는 이산화탄소(CO2)의 배출과정에서 내화물에 미세기공을 형성시키게 되고, 이러한 미세기공은 내화물의 균열전파를 막을 수 있고, 내스폴링성을 높일 수 있다. In addition, carbon dioxide (CO 2 ) generated by the chemical reaction represented by the reaction scheme 1 is discharged to the outside of the refractory. In the process of discharging carbon dioxide (CO 2 ) is discharged to form a fine pore in the refractory, the fine pores can prevent crack propagation of the refractory, it is possible to increase the spalling resistance.
이하, 본 발명의 이해를 돕기 위하여 바람직한 실시예를 제시하나, 하기 실시예는 본 발명을 예시하는 것일 뿐 본 발명의 범위가 하기 실시예에 한정되는 것은 아니다.Hereinafter, the present invention will be described in more detail with reference to the following examples. However, the scope of the present invention is not limited to the following examples.
[실시예 1] Example 1
액상 페놀수지 100중량부와 TiO2분체(입도: 325mesh) 20중량부를 혼합하였다. 상기에서 혼합된 혼합물을 질소분위기하에서 1400℃의 온도로 1시간동안 열처리를 행하여, 탄소입자를 제조하였고, 이렇게 제조된 실시예 1에 따른 탄소입자의 결정 면간격(X선 회절에 의한 결정 면간격을 학진법으로 측정)은 d002 = 0.336nm이 었다. 100 parts by weight of the liquid phenol resin and 20 parts by weight of TiO 2 powder (particle size: 325 mesh) were mixed. The mixed mixture was heat-treated at a temperature of 1400 ° C. for 1 hour under a nitrogen atmosphere to prepare carbon particles, and crystal plane spacing of the carbon particles according to Example 1 thus prepared (crystal plane spacing by X-ray diffraction). Measured by the school method) was d 002 = 0.336 nm.
[비교예 1] Comparative Example 1
액상 페놀수지 100중량부를 질소분위기하에서 900~1550℃의 온도로1시간동안 열처리를 행하여, 탄소입자를 제조하였고, 이렇게 제조된 비교예1에 따른 탄소입자의 결정 면간격(X선 회절에 의한 결정 면간격을 학진법으로 측정)은 d002 = 0.340nm이었다.100 parts by weight of the liquid phenolic resin was heat-treated under a nitrogen atmosphere at a temperature of 900 to 1550 ° C. for 1 hour to prepare carbon particles, and crystal plane spacing of carbon particles according to Comparative Example 1 thus prepared (crystallization by X-ray diffraction). The plane spacing was measured by the academic method), d 002 = 0.340 nm.
상기에서 보인 바와 같이, TiO2를 함유하지 않은 비교예 1에 따른 탄소입자의 면간격은 0.340nm이상을 나타내었으나, TiO2가 첨가된 실시예 1에 따른 탄소입자의 결정 면간격은 0.340nm 부근으로 흑연화가 진행되었음을 확인할 수 있었다.As shown above, the surface spacing of the carbon particles according to Comparative Example 1 containing no TiO 2 was 0.340 nm or more, but the crystal surface spacing of the carbon particles according to Example 1 to which TiO 2 was added was about 0.340 nm. It was confirmed that graphitization proceeded.
Claims (19)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020090133462A KR101223845B1 (en) | 2009-12-29 | 2009-12-29 | Binder composition for carbon based refractory, carbon based refractory composition, carbon based refractory and method for producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020090133462A KR101223845B1 (en) | 2009-12-29 | 2009-12-29 | Binder composition for carbon based refractory, carbon based refractory composition, carbon based refractory and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20110076702A true KR20110076702A (en) | 2011-07-06 |
KR101223845B1 KR101223845B1 (en) | 2013-01-17 |
Family
ID=44916575
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020090133462A KR101223845B1 (en) | 2009-12-29 | 2009-12-29 | Binder composition for carbon based refractory, carbon based refractory composition, carbon based refractory and method for producing the same |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR101223845B1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101530263B1 (en) * | 2011-09-09 | 2015-06-29 | 풀 부르스 에스.에이. | Ramming mass for the refractory coating of a metallurgical vessel, method for implementing same and metallurgical vessel, in particular a blast furnace, comprising a coating using said ramming mass |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08169766A (en) * | 1994-12-15 | 1996-07-02 | Nippon Steel Corp | Starting material for refractory, binder for refractory and production of refractory |
-
2009
- 2009-12-29 KR KR1020090133462A patent/KR101223845B1/en active IP Right Grant
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101530263B1 (en) * | 2011-09-09 | 2015-06-29 | 풀 부르스 에스.에이. | Ramming mass for the refractory coating of a metallurgical vessel, method for implementing same and metallurgical vessel, in particular a blast furnace, comprising a coating using said ramming mass |
Also Published As
Publication number | Publication date |
---|---|
KR101223845B1 (en) | 2013-01-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Jin et al. | Highly transparent AlON pressurelessly sintered from powder synthesized by a novel carbothermal nitridation method | |
Lian et al. | Effect of in situ synthesized SiC whiskers and mullite phases on the thermo-mechanical properties of Al2O3–SiC–C refractories | |
CN101903305B (en) | Mix and refractory product having a high hydration resistance produced therefrom | |
Nanda et al. | Raw materials, microstructure, and properties of MgO–C refractories: directions for refractory recipe development | |
WO2010095637A1 (en) | Unburned alumina-carbon brick and kiln facility utilizing same | |
CN103664199B (en) | Take Polycarbosilane as the method that carborundum refractory prepared by bonding agent | |
CN102115335A (en) | Novel abrasion resistant silicon-mullite-nitrogen brick for transition zones of rotary cement kiln | |
KR101544861B1 (en) | Aluminum oxycarbide composition and process for producing same, and refractory | |
CN107954710B (en) | Silicon carbide and calcium titanium aluminate combined complex-phase refractory material and preparation method thereof | |
Talabi et al. | Synthesis and graphitization of resole resins by ferrocene | |
CN104276831B (en) | A kind of method preparing calcium oxide carbon brick | |
CN104261840B (en) | A kind of phosphate combines low aluminum silicon not brick and preparation method thereof | |
KR101223845B1 (en) | Binder composition for carbon based refractory, carbon based refractory composition, carbon based refractory and method for producing the same | |
CN109608200A (en) | A kind of carbon silicated aluminum combination SiC fire resistant materials and preparation method thereof | |
CN112500130A (en) | Silicon-calcium-barium complex phase combined silicon carbide magnesia-carbon brick and manufacturing method thereof | |
CN106220193A (en) | A kind of silicon carbide brick | |
JP5126984B2 (en) | Method for producing SiC-containing castable refractory | |
JP5331077B2 (en) | Carbon-containing refractories | |
JP2012066986A (en) | Aluminum oxycarbide composition and method for producing the same | |
JP2011016667A (en) | Ferrosilicon nitride powder and refractory | |
JP2617086B2 (en) | Silicon carbide casting material | |
JP4160796B2 (en) | High thermal shock resistant sliding nozzle plate brick | |
JP2003171184A (en) | SiC FOR MONOLITHIC REFRACTORY HAVING EXCELLENT CORROSION RESISTANCE, SPALLING RESISTANCE AND DRYNESS, PRODUCTION METHOD THEREFOR, AND RAW MATERIAL FOR THE MONOLITHIC REFRACTORY | |
KR100503353B1 (en) | CHEMICAL COMPOSITION FOR MgO-CARBON REFRACTORY | |
KR20000006654A (en) | MgO-C BASED REFRACTORY |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
E90F | Notification of reason for final refusal | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant | ||
FPAY | Annual fee payment |
Payment date: 20160107 Year of fee payment: 4 |
|
FPAY | Annual fee payment |
Payment date: 20170110 Year of fee payment: 5 |
|
FPAY | Annual fee payment |
Payment date: 20180111 Year of fee payment: 6 |
|
FPAY | Annual fee payment |
Payment date: 20190109 Year of fee payment: 7 |