KR100310050B1 - method for forming canbon brick with fire resistance and corrosion resestance - Google Patents

method for forming canbon brick with fire resistance and corrosion resestance Download PDF

Info

Publication number
KR100310050B1
KR100310050B1 KR1019990004069A KR19990004069A KR100310050B1 KR 100310050 B1 KR100310050 B1 KR 100310050B1 KR 1019990004069 A KR1019990004069 A KR 1019990004069A KR 19990004069 A KR19990004069 A KR 19990004069A KR 100310050 B1 KR100310050 B1 KR 100310050B1
Authority
KR
South Korea
Prior art keywords
weight
parts
corrosion
carbon
graphite
Prior art date
Application number
KR1019990004069A
Other languages
Korean (ko)
Other versions
KR20000055447A (en
Inventor
정해룡
범진형
Original Assignee
한종웅
조선내화 주식회사
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 한종웅, 조선내화 주식회사 filed Critical 한종웅
Priority to KR1019990004069A priority Critical patent/KR100310050B1/en
Publication of KR20000055447A publication Critical patent/KR20000055447A/en
Application granted granted Critical
Publication of KR100310050B1 publication Critical patent/KR100310050B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/515Shaped 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
    • C04B35/52Shaped 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
    • C04B35/522Graphite
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/626Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/63Preparing 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
    • C04B35/632Organic additives
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/64Burning or sintering processes
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/40Metallic constituents or additives not added as binding phase
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/65Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
    • C04B2235/656Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes characterised by specific heating conditions during heat treatment
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance

Abstract

본 발명은 내산성, 내부식성, 내열성을 갖는 각종 화학공장의 내산탱크, 용해로의 내화물 등에 대하여 우수한 특성을 갖게함과 함께 공정의 단순화 및 저온의 열처리에 따라 생산원가를 절감하는데 적합한 카본 벽돌의 제조에 관한 것이다.The present invention has excellent properties for acid tanks of various chemical plants, refractory materials of melting furnaces, etc. having acid resistance, corrosion resistance, and heat resistance, and in the manufacture of carbon bricks suitable for reducing the production cost according to the simplification of the process and low temperature heat treatment. It is about.

이에 따른 본 발명은 피치(pitch) 또는 콜타르(coal tar)를 가열 만든 인조흑연 30-95 중량부, 금속규소(Si) 2-25 중량부, 비정질카본, 인상흑연 또는 천연흑연, 금속산화물 중 적어도 1종 이상 2-20 중량부, 열경화성수지 3-15 중량부 혼련하여 성형한 후 환원성 분위기에서 1,200-1700℃ 온도로 3-72시간 소성함을 특징으로 하는 내화성 및 내식성 카본 벽돌의 제조방법에 관한 기술이다.Accordingly, the present invention is 30-95 parts by weight of artificial graphite made by heating a pitch or coal tar, 2-25 parts by weight of metal silicon (Si), amorphous carbon, impression graphite or natural graphite, at least one of metal oxide 2-20 parts by weight of one or more, 3-15 parts by weight of the thermosetting resin after kneading and molding for a method of producing a fire-resistant and corrosion-resistant carbon brick, characterized in that the firing 3-72 hours at a temperature of 1,200-1700 ℃ in a reducing atmosphere Technology.

Description

내화성 및 내식성 카본 벽돌의 제조방법{method for forming canbon brick with fire resistance and corrosion resestance}Method for forming fire and corrosion resistant carbon bricks {method for forming canbon brick with fire resistance and corrosion resestance}

본 발명은 카본 벽돌에 관한 것으로서, 보다 상세하게는 피치(pitch) 또는 콜타르(coal tar)를 가열하여 만든 인조흑연 원료인 주성분과 금속규소 등의 원료로 하여 낮은 온도에서 열처리함으로서, 불순물의 함량이 낮고 기존의 카본 벽돌에 비해 내산성 및 강도특성이 우수하며 제조공정의 간단화 및 고온에서의 흑연화 공정의 생략으로 절감된 제조원가에 적합한 카본 벽돌의 제방법에 관한 것이다.The present invention relates to a carbon brick, and more particularly, by heat-treating at a low temperature by using a raw material such as a main component and a metal silicon, which is an artificial graphite raw material made by heating a pitch or coal tar, the content of impurities is increased. It is low and excellent in acid resistance and strength characteristics compared to the existing carbon brick, and relates to a method of manufacturing a carbon brick suitable for the production cost reduced by the simplification of the manufacturing process and the elimination of the graphitization process at a high temperature.

카본 벽돌은 내산성, 내부식성, 열전도율 등이 우수하여 각종 화학공장의 내산탱크, 고로노저(高爐爐底) 내화물, 철강 및 비철 등의 유도로(誘導爐)용 내화물, 비철금속 제련공장의 귀금속 회수목적의 굴뚝 등 그 사용도가 다양하다.Carbon brick has excellent acid resistance, corrosion resistance, and thermal conductivity, so it is possible to recover acid tanks of various chemical plants, blast furnace refractory materials, induction furnaces for steel and non-ferrous metals, and precious metals in nonferrous metal smelting plants. Chimney and its use is also varied.

카본 벽돌의 제조방법은 여러 종류가 있으나, 통상적으로는 출발원료로 침상 코크스(Needle Cokes)나 저온 열처리 코크스 등 흑연이 아닌 비결정상의 카본을 주성분으로 하여 열가소성수지(예: 피치타르)를 열간 혼련하고, 열간 성형한 후 1,500-3,000℃ 정도의 흑연 화로에서 전기통전 방식으로 가열하여 비결정상의 카본을 흑연화시켜 제조하고 있다.There are many methods for producing carbon bricks. Generally, starting materials are hot kneaded thermoplastics (eg, pitch tar) based on amorphous carbon, such as needle cokes or low temperature heat treated cokes, as non-graphite carbon. After the hot forming, the graphite is heated in an electric furnace at about 1,500 to 3,000 ° C. to form amorphous carbon.

이와 같은 종래의 방법은 열가소성수지를 20% 이상 사용하여 열간에서 혼련 및 통전가열에 2-4일, 냉간에 1-2주간을 하는 등 제조공정이 길고 복잡하는 등 제조경비가 높다는 단점을 가지고 있으며, 특히 화학공장 등의 내산탱크에 사용되는 카본 함량이 92% 가량인 카본 벽돌의 경우는 출발원료로 저급 침상 코크스나 저온 열처리 코크스 사용으로 불순물의 함량이 높고, 1,600℃ 이하의 열처리시에는 흑연화 정도가 낮기 때문에 강도 보강 목적으로 점토 등을 사용하여 사용되는 산 종류에 따라 장시간 사용시 취약해질 가능성이 높다.Such a conventional method has a disadvantage in that the manufacturing cost is high, such as the use of 20% or more of thermoplastic resin for 2-4 days for hot kneading and energizing heating and 1-2 weeks for cold, such as a long and complicated manufacturing process. In particular, carbon bricks containing about 92% of the carbon used in acid tanks in chemical plants have high impurity content by using low needle coke or low temperature heat-treated coke as starting materials, and graphitization during heat treatment below 1,600 ℃. Because of the low level, it is highly likely to be vulnerable when used for a long time depending on the type of acid used for the purpose of strength reinforcement.

본 발명은 상기한 종래의 문제점을 해결하기 위한 것으로, 출발원료로 피치 (pitch)또는 콜타르(coal tar)를 가열하여 만든 인조흑연인 주성분과 금속규소 및 열경화성수지를 사용하여 기존에 비해 낮은 온도에서 열처리하므로써 에너지절약 측면에서 유리하고, 냉간에서 성형 가능하는 등 제조공정의 단순화로 제조원가의 절감효과를 갖음과 함께 우수한 내산성 및 강도특성을 갖는 카본 벽돌을 얻고자 하는데 그 목적이 있다.The present invention is to solve the above-mentioned problems, using the artificial graphite main component made by heating the pitch (pitch) or coal tar (coal tar) as a starting material and metal silicon and thermosetting resin at a lower temperature than conventional It is an object of the present invention to obtain a carbon brick having an excellent acid resistance and strength characteristics as well as a reduction in manufacturing cost by simplifying the manufacturing process, such as being advantageous in terms of energy saving and cold forming by heat treatment.

상기한 목적을 달성하기 위한 본 발명은 피치(pitch) 또는 콜타르(coal tar)를 가열하여 만든 인조흑연 30-95 중량부, 금속규소(Si) 2-25 중량부, 비정질카본, 인상흑연 또는 천연흑연, 금속산화물 중 적어도 1종 이상 2-20 중량부, 열경화성수지 3-15 중량부 혼련하여 성형한 후 환원성 분위기에서 1,200-1,700℃ 온도로 3-72시간 소성하여서 됨을 특징으로 하는 내화성 및 내식성 카본 벽돌의 제조방법으로 이루어 진다.The present invention for achieving the above object is 30-95 parts by weight of artificial graphite made by heating the pitch (pitch) or coal tar (coal tar), 2-25 parts by weight of metal silicon (Si), amorphous carbon, impression graphite or natural 2-20 parts by weight of at least one of graphite and metal oxides, 3-15 parts by weight of thermosetting resins are kneaded and then fired for 3 to 72 hours at a temperature of 1,200-1,700 ° C. in a reducing atmosphere. It is made of brick manufacturing method.

본 발명은 소성중에 카본과 금속규소가 반응하여 입자와 입자 사이에서 베타 탄화규소(β-SiC) 및 산질화규소(Siliconoxynitride)(Si2ON2)를 생성시켜 입자와 입자가 결정되며, 소성 분위기내 일산화탄소(CO)와 금속규소가 반응하여 베타 탄화규소를 생성한다.상기와 같은 환원성분위기중에는 공기가 혼입되어 있으며, 공기중에는 질소가 혼재하고 있다. 따라서 그와 같은 환원성 분위기에서 열처리함로서 산질화규소 (Siliconoxynitride)(Si2ON2)가 생성된다.In the present invention, carbon and metal silicon react during firing to produce beta silicon carbide (β-SiC) and silicon oxynitride (Si 2 ON 2 ) between the particles and the particles to determine the particles and particles, and in the firing atmosphere Carbon monoxide (CO) and metal silicon react to produce beta silicon carbide. In the above-mentioned reducing atmosphere, air is mixed and nitrogen is mixed in the air. Therefore, silicon oxynitride (Si 2 ON 2 ) is produced by heat treatment in such a reducing atmosphere.

이렇게 생성된 베타형 탄화규소는 카본 벽돌의 기공내에 휘스커나 파이버상으로 잘 발달되어 결합강도를 더욱 강화시킨다.The beta-type silicon carbide thus produced is well developed in whiskers or fibers in the pores of the carbon brick to further strengthen the bond strength.

즉, 탄화규소 휘스커나 파이버 등이 소성과정에서 생성되어 흑연 큰 입자와 작은 입자를 더욱 강하게 결합시킨다.That is, silicon carbide whiskers or fibers are produced during the firing process to bond the graphite large particles and small particles more strongly.

따라서 흑연화 공정을 거치는 기존의 방법에 의해 제조된 제품들 보다 제조공정이 단순하면서 제조 경비가 저렴한 방법으로 우수한 특성의 카본 벽돌을 제조할 수 있었다.Therefore, carbon bricks having excellent characteristics could be manufactured by a simpler manufacturing process and a lower manufacturing cost than products manufactured by conventional methods of graphitization.

본 발명에서는 소성온도를 대폭 낮추었는데 그 원인은 기존 방법에서는 비결정질 카본 원료인 침상 코크스 등을 사용하여 판상의 적층 구조인 흑연화가 1,500℃ 이상에서 시작되고 2,000℃ 이상에서 비로서 위와 같은 흑연화 결정 구조를 갖게 되는데, 본 발명의 제조방법은 출발원료 자체가 위의 흑연화 결정 구조를 갖고 있기 때문에 별도의 흑연화 공정이 필요없고 첨가된 금속규소가 소성중에 베타 탄화규소와 산질화규소를 생성하여 흑연화 결정 구조를 가진 입자와 입자의 결합을 이루어 기존의 카본 벽돌보다 우수한 강도특성을 나타낸 것이다.In the present invention, the firing temperature is significantly lowered. The reason for this is that in the conventional method, graphitization, which is a plate-like layered structure using needle-like coke, which is an amorphous carbon raw material, starts at 1,500 ° C or higher, and at 2,000 ° C or higher, such graphitized crystal structure. In the production method of the present invention, since the starting material itself has the above graphitized crystal structure, a separate graphitization step is not necessary and the added metal silicon is graphitized by producing beta silicon carbide and silicon oxynitride during firing. The combination of particles and particles with a crystalline structure showed better strength properties than conventional carbon bricks.

다음은 실시예에 따라 설명한다.The following is described according to the embodiment.

(실시예 1)(Example 1)

원료 배합비, 인조흑연 90중량부, 금속규소 5중량부, 인상흑연 5중량부Raw material blending ratio, artificial graphite 90 parts by weight, metal silicon 5 parts by weight, impression graphite 5 parts by weight

결합재 1-10중량부1-10 parts by weight of binder

입도분포 : 금속규소 10㎛Particle Size Distribution: Metal Silicon 10㎛

결합제를 제외한 원료 전체 입도분포 : 1㎜ 이상 35%, 1-0.212㎜ 30%, 0,212㎜ 이하 35%Total particle size distribution of raw materials excluding binder: 1mm or more 35%, 1-0.212mm 30%, 0,212mm or less 35%

소성조건, 온도 : 1,500℃Firing condition, temperature: 1,500 ℃

시간 : 10시간Time: 10 hours

상기 조건은 (표 1)의 시료(다)를 나타낸 것으로, 상기 원료를 배합하고 혼합기에서 무가압 혼련한 후 혼합 배토를 상온에서 24시간 숙성한다.The above conditions are shown in the sample (C) of (Table 1), and the raw materials are blended and kneaded in a mixer without pressure, and the mixed clay is aged at room temperature for 24 hours.

상기 숙성된 혼합 배토를 평량한 후 한국 공업 규격에 표시된 형태와 이형으로 성형하여 상온에서 하루정도의 자연건조를 행한다.After the maturation of the mixed mixed clay is molded into the shape and mold release indicated in the Korean Industrial Standards, the natural drying is performed at room temperature for about one day.

자연 건조된 성형체를 100-200℃에서 24시간 동안 건조를 행한다.The naturally dried molded body is dried at 100-200 ° C. for 24 hours.

건조된 성형체를 1,500℃에서 10시간 소성한다.The dried molded body is calcined at 1,500 ° C for 10 hours.

소성 킬른은 단가마와 텐널킬른 모두 가능하며, 턴넬킬른에서 소성할 경우 대량생산이 기능하게 되어 생산성 향상과 품질 균일화 측면에서 큰 효과를 나타낸다.Firing kilns are available in both kilns and tennel kilns, and when fired in tunnel kilns, mass production functions, resulting in greater productivity and quality uniformity.

상기와 같은 조건에 따라 나타난 물리적 성질은 기공율 18%, 흡수율 9.5%, 곡강도 220㎏/㎠, 압축강도 300㎏/㎠에 비하여 우수함을 알 수 있었다.The physical properties shown by the above conditions were found to be superior to the porosity of 18%, the absorption rate of 9.5%, bending strength 220㎏ / ㎠, compressive strength 300kg / ㎠.

(실시예 2)(Example 2)

원료 배합비, 인조흑연 80중량부, 인상흑연 10중량부, 금속규소 10중량부Raw material blending ratio, artificial graphite 80 parts by weight, impression graphite 10 parts by weight, metal silicon 10 parts by weight

결합재 1-10중량부1-10 parts by weight of binder

입도분포 : 금속규소 10㎛Particle Size Distribution: Metal Silicon 10㎛

결합제를 제외한 원료 전체 입도분포 : 1㎜ 이상 35%, 1-0.212㎜ 25%, 0,212㎜ 이하 40%Total particle size distribution of raw materials excluding binder: 1mm or more 35%, 1-0.212mm 25%, 0,212mm or less 40%

소성조건, 온도 : 1,500℃Firing condition, temperature: 1,500 ℃

시간 : 10시간Time: 10 hours

상기 조건은 (표1)의 시료(아)를 나타낸 것으로 그외 조건은 실시예 1과 동일하게 하였다.The said conditions showed the sample (a) of (Table 1), and other conditions were made the same as Example 1.

상기와 같은 조건에 따라 나타난 물리적 성질은 기공율 17%, 흡수율 9%, 곡강도 180㎏/㎠, 압축강도 350㎏/㎠ 로서 기존 기술에 비해 우수하게 나타났다.The physical properties shown by the above conditions were porosity 17%, absorption 9%, bending strength 180㎏ / ㎠, compressive strength 350㎏ / ㎠ showed better than the existing technology.

(표 1)Table 1

구 분division end I All la hemp bar four Ah character car Ka Ta wave Ha 인조흑연원료Artificial Graphite Raw Material 9898 9595 9090 8585 8585 8383 8383 8080 8080 8080 6565 6565 5555 5555 금속규소Metal silicon 22 33 55 55 77 77 1010 1010 1313 1515 1515 2020 2020 2525 인상흑연Impression 00 22 55 1010 88 1010 77 1010 77 55 2020 1515 2525 2020 결합제(외 첨가)Binder (external addition) 1-10중량부1-10 parts by weight 소성온도(℃)Firing temperature (℃) 1,200-1,600℃1,200-1,600 ℃ 소성시간(H)Firing time (H) 3-723-72

상기 실시예 1,2(시료 : 다, 아)를 비롯한 (표 1)에 나타낸 다른 실시예(시료 : 가-나, 라-사, 차-하)에 따른 조건을 실시한 바, (표 2)와 같은 결과가 나타났다.The conditions according to the other examples shown in Table 1, including Examples 1 and 2 (Samples: c, a), were carried out. (Table 2) The same result was obtained.

이상에서와 같이 본 발명은 기존의 기술과 다른 방법으로 카본 벽돌을 제조하여 우수한 특성의 제품을 얻을 수 있다.As described above, the present invention can obtain a product having excellent properties by producing carbon bricks by a method different from the existing technology.

본 발명은 기존의 방법보다 제조공정이 단순하고 상기 제조공정시 기존의 방법보다 고온을 필요로 하지 않기 때문에 에너지 절약적인 측면에서도 유리한 방법이라고 생각된다.The present invention is considered to be an advantageous method in terms of energy saving since the manufacturing process is simpler than the existing method and does not require a higher temperature than the existing method in the manufacturing process.

또한, 혼련이나 성형 건조 공정에서 열경화성수지를 사용하므로서 혼련 성형공정을 일반적으로 내화벽돌의 혼련 성형과 같이 냉간에서 가능하게 하였고, 건조공정도 기존 방법인 열경화성수지를 사용하여 장시간 건조하는 것을 대폭적으로 줄일 수 있었다.In addition, by using the thermosetting resin in the kneading or molding drying process, the kneading molding process is generally possible in the cold like kneading molding of the refractory brick, and the drying process is drastically reduced for a long time by using the conventional thermosetting resin. Could.

(표 2)Table 2

구 분division end I All la hemp bar four Ah character car Ka Ta wave Ha 부피비중Volume specific gravity 1.721.72 1.721.72 1.721.72 1.711.71 1.731.73 1.731.73 1.721.72 1.731.73 1.751.75 1.781.78 1.801.80 1.811.81 1.851.85 1.871.87 기공율(%)Porosity (%) 18.218.2 18.818.8 1818 1919 19.519.5 2020 1919 1717 2121 20.520.5 2020 22.322.3 2222 2323 흡수율(%)Absorption rate (%) 9.79.7 1010 9.59.5 1010 10.510.5 1111 9.89.8 99 10.510.5 1111 10.810.8 1111 1111 1212 곡강도(㎏/㎠)Bending strength (㎏ / ㎠) 158158 179179 220220 154154 178178 179179 196196 211211 191191 175175 165165 151151 130130 141141 압축강도(㎏/㎠)Compressive strength (㎏ / ㎠) 245245 315315 443443 293293 346346 295295 320320 415415 382382 380380 376376 380380 392392 311311

이상에서와 같이 본 발명은 기존 방법과는 다르게 피치 또는 콜타르를 가열하여 만든 인조흑연 원료와 금속규소를 첨가하고 열경화수지로 혼련, 성형후 환원성 분위기에서 저온으로 조성함으로서 공정의 간단화 및 에너지 절감으로 생산원가를 절감함과 함께 우수한 내산성 및 강도특성을 갖는 카본 벽돌을 얻게 된다.As described above, the present invention, unlike the conventional method, adds artificial graphite raw material and metal silicon made by heating pitch or coal tar, kneading with thermosetting resin, and forming at low temperature in a reducing atmosphere after molding, thereby simplifying the process and saving energy. As a result, carbon bricks having excellent acid resistance and strength characteristics can be obtained while reducing production costs.

Claims (1)

피치(pitch) 또는 콜타르(coal tar)를 가열하여 만든 인조흑연 30-95 중량부, 금속규소(Si) 2-25 중량부, 비정질카본, 인상흑연 또는 천연흑연, 금속산화물 중 적어도 1종 이상 2-20 중량부, 열경화성수지 3-15 중량부 혼련하여 성형한 후 환원성 분위기에서 1,200-1,700℃ 온도로 3-72시간 소성하여서 됨을 특징으로 하는 내화성 및 내식성 카본 벽돌의 제조방법.30-95 parts by weight of artificial graphite made by heating pitch or coal tar, 2-25 parts by weight of silicon (Si), amorphous carbon, impression graphite or natural graphite, at least one or more of metal oxides 2 -20 parts by weight, thermosetting resin 3-15 parts by weight kneading and molding, and then fired for 3 to 72 hours at a temperature of 1,200-1,700 ℃ in a reducing atmosphere characterized in that the manufacturing method of the fire-resistant and corrosion-resistant carbon brick.
KR1019990004069A 1999-02-06 1999-02-06 method for forming canbon brick with fire resistance and corrosion resestance KR100310050B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019990004069A KR100310050B1 (en) 1999-02-06 1999-02-06 method for forming canbon brick with fire resistance and corrosion resestance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019990004069A KR100310050B1 (en) 1999-02-06 1999-02-06 method for forming canbon brick with fire resistance and corrosion resestance

Publications (2)

Publication Number Publication Date
KR20000055447A KR20000055447A (en) 2000-09-05
KR100310050B1 true KR100310050B1 (en) 2001-10-17

Family

ID=19573588

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019990004069A KR100310050B1 (en) 1999-02-06 1999-02-06 method for forming canbon brick with fire resistance and corrosion resestance

Country Status (1)

Country Link
KR (1) KR100310050B1 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100471356B1 (en) * 2001-07-06 2005-03-08 조선내화 주식회사 carbon for refractories & refractories with carbon
KR101392720B1 (en) * 2013-03-21 2014-05-14 (주)포스코켐텍 Composition for high-temperature adhesive the refractory brick having execellent bonding strength
CN116656022B (en) * 2023-05-30 2024-01-02 荣成荣鹰橡胶制品有限公司 Solid tire tread rubber and preparation method thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03205362A (en) * 1989-12-28 1991-09-06 Kawasaki Refract Co Ltd Graphite-silicon carbide refractory brick and production thereof

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03205362A (en) * 1989-12-28 1991-09-06 Kawasaki Refract Co Ltd Graphite-silicon carbide refractory brick and production thereof

Also Published As

Publication number Publication date
KR20000055447A (en) 2000-09-05

Similar Documents

Publication Publication Date Title
CN100457681C (en) High conductive high strength graphite brick for ultralarge blast furnace, its production technology and application
US2752258A (en) Silicon nitride-bonded silicon carbide refractories
KR940011452B1 (en) Silicon carbide refractories having modified silicon nitride bond
CN101734936A (en) Preparation method of Si3N4-SiC-C fire-resistant material powder
US2636826A (en) Silicon carbide refractory
CN107954697A (en) A kind of magnesia carbon brick for adding boron carbide and preparation method thereof
CN1050591C (en) Fired microporous carbon-aluminium brick
CN112457031A (en) Low-creep high-alumina brick and preparation method thereof
KR100310050B1 (en) method for forming canbon brick with fire resistance and corrosion resestance
CN101591190A (en) A kind of aluminum electrolytic bath side wall New Si 3N 4-SiC-C refractory brick and preparation method thereof
JPH07187755A (en) Refractory ceramic molding compound
CN109265144A (en) A kind of converter body brick and preparation method thereof adding titanium nitride
KR920005409B1 (en) Preparing method of carbon/ceramic composite
KR930011260B1 (en) Method of firebrick use with fly ash
CN111233499A (en) SiC/C homogeneous material, stemming and preparation method thereof
JP2000191363A (en) Spalling resistant spinel brick
CN116283315B (en) Carbon-free inorganic pressed spinel sliding plate brick and preparation method thereof
JPS5839798B2 (en) Method for producing coal-fired firebrick
KR970008735B1 (en) Process for the preparation of burned material using slug
JPH11292615A (en) Crucible for melted metal and its production
CN116639963A (en) Refractory castable for blast furnace cast house iron runner and preparation method thereof
JPH04139057A (en) Wear resistant refractory
JP3382702B2 (en) Setter and its manufacturing method
JPS59107982A (en) Highly antispalling zirconia refractories
JPH0354155A (en) Production of graphite-containing brick for lining of melted metallic vessel

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20120802

Year of fee payment: 12

FPAY Annual fee payment

Payment date: 20130801

Year of fee payment: 13

LAPS Lapse due to unpaid annual fee