JPH0137839B2 - - Google Patents
Info
- Publication number
- JPH0137839B2 JPH0137839B2 JP58217623A JP21762383A JPH0137839B2 JP H0137839 B2 JPH0137839 B2 JP H0137839B2 JP 58217623 A JP58217623 A JP 58217623A JP 21762383 A JP21762383 A JP 21762383A JP H0137839 B2 JPH0137839 B2 JP H0137839B2
- Authority
- JP
- Japan
- Prior art keywords
- electrode
- boron
- anthracite
- coke
- hour
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 13
- 229910052796 boron Inorganic materials 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 9
- RHZUVFJBSILHOK-UHFFFAOYSA-N anthracen-1-ylmethanolate Chemical compound C1=CC=C2C=C3C(C[O-])=CC=CC3=CC2=C1 RHZUVFJBSILHOK-UHFFFAOYSA-N 0.000 claims description 8
- 239000003830 anthracite Substances 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 239000000571 coke Substances 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 229910002804 graphite Inorganic materials 0.000 claims description 4
- 239000010439 graphite Substances 0.000 claims description 4
- 239000002802 bituminous coal Substances 0.000 claims description 3
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical group B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000003077 lignite Substances 0.000 claims description 3
- 238000001354 calcination Methods 0.000 claims description 2
- 229910052580 B4C Inorganic materials 0.000 claims 1
- 239000003575 carbonaceous material Substances 0.000 claims 1
- 239000002006 petroleum coke Substances 0.000 description 6
- 238000001125 extrusion Methods 0.000 description 5
- 238000005087 graphitization Methods 0.000 description 3
- 238000012856 packing Methods 0.000 description 3
- 239000011295 pitch Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 150000001639 boron compounds Chemical class 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 238000010891 electric arc Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229910015245 B4Si Inorganic materials 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- ZDVYABSQRRRIOJ-UHFFFAOYSA-N boron;iron Chemical compound [Fe]#B ZDVYABSQRRRIOJ-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000011301 petroleum pitch Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- NUSDCJCJVURPFV-UHFFFAOYSA-N silicon tetraboride Chemical compound B12B3B4[Si]32B41 NUSDCJCJVURPFV-UHFFFAOYSA-N 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B7/00—Heating by electric discharge
- H05B7/02—Details
- H05B7/06—Electrodes
- H05B7/08—Electrodes non-consumable
- H05B7/085—Electrodes non-consumable mainly consisting of carbon
Landscapes
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Plasma & Fusion (AREA)
- Ceramic Products (AREA)
- Vertical, Hearth, Or Arc Furnaces (AREA)
- Furnace Details (AREA)
- Discharge Heating (AREA)
- Electrodes For Compound Or Non-Metal Manufacture (AREA)
- Carbon And Carbon Compounds (AREA)
Description
発明の分野
本発明はアーク炉用の黒鉛電極の独特な製造方
法およびこの方法を実施して得られた独特な電極
に関するものである。
先行技術の記述
アーク炉による製鋼用の電極を製造する際にプ
レミアム石油コークスが広く使用されている。し
かしこの種のコークスの価格が非常に急速に高騰
しており、このことが今後のアーク炉の使用、従
つてアーク電極の市場の発展に大きく影響するも
のと思われる。無煙炭、歴青炭、亜炭、いわゆる
No.2、No.3コークスなどの安価な炭素質原料をア
ーク炉用電極の製造に関してテストしたが、これ
らの物質から得られた電極の特性はプレミアム石
油コークスから作られた電極と比較してきわめて
劣悪であり、これらの電極は電気炉に使用するに
は不適当であつた。炭素質原料としての全石油コ
ークス以外の原料から作られた電極の特性を許容
水準まで上昇させる努力は今日まで不成功であつ
た。
本発明の主目的は、炭素質原料が必ずしも全部
プレミアムグレードの石油コークスでないアーク
炉中において使用するに適した電極の製造法を提
供するにある。
本発明の要約
本発明は、他の点では通常の電極製造工程にお
いて、プレミアム石油コークス以外の炭素質原
料、好ましくは無煙炭に対して、元素ホウ素また
はホウ素化合物、好ましくは炭化ホウ素(B4C)
の作用を加えることによつて、無煙炭の非常に無
秩序な構造を非常に黒鉛的な構造に変形するにあ
る。
本発明の詳細な説明
本発明の実施に際して、非石油コークス炭素質
原料の粒子を通常のピツチ結合剤および潤滑剤と
混合し、この混合物に対して元素ホウ素またはホ
ウ素含有化合物を添加する。無煙炭以外の適当な
炭素質原料は歴青炭、亜炭およびNo.2とNo.3コー
クスである。好ましくはホウ素原料は、製造工程
中に黒鉛化段階に際して炭素質原料と反応する際
にガス副生物を放出しないものとする。この様な
ホウ素原料は元素ホウ素、炭化ホウ素(B4C)、
四ホウ化ケイ素(B4Si)およびホウ化鉄(FeB)
である。またホウ素物質は、カ焼中の炭素質原料
と組合わせることができ、この方法においては、
ホウ素化合物はホウ酸(H3BO3)または酸化ホ
ウ素(B2O3)などの酸化物とすることができる。
なぜかなら、この場合に発生するガス副生物は仕
上り電極の構造一体性に影響しないからである。
実施例
6インチ径の粗粒無煙炭電極を押出法によつて
作製した。粉砕と分粒に先立つて無煙炭を2200℃
でカ焼した。粉炭、ピツチ、潤滑剤、およびミツ
クスに対するB4C添加剤は下表に示されてい
る。対照ミツクスはホウ素を含有していなかつた
が、ホウ素化試料片のミツクスは、約3重量%の
ホウ素を有する仕上り製品を生じる様に配合され
ていた。
FIELD OF THE INVENTION The present invention relates to a unique method for manufacturing graphite electrodes for electric arc furnaces and to the unique electrodes obtained by implementing this method. Description of the Prior Art Premium petroleum coke is widely used in producing electrodes for arc furnace steelmaking. However, the price of this type of coke is rising very rapidly, and this is expected to have a major impact on the future use of arc furnaces and, therefore, on the development of the market for arc electrodes. Anthracite, bituminous coal, lignite, so-called
Inexpensive carbonaceous feedstocks such as No. 2 and No. 3 cokes have been tested for the production of arc furnace electrodes, but the properties of electrodes obtained from these materials are not as good as those made from premium petroleum coke. These electrodes were extremely poor and unsuitable for use in electric furnaces. Efforts to raise the properties of electrodes made from feedstocks other than whole petroleum coke as a carbonaceous feedstock to acceptable levels have been unsuccessful to date. The main object of the present invention is to provide a method for producing an electrode suitable for use in an electric arc furnace where the carbonaceous feedstock is not necessarily all premium grade petroleum coke. SUMMARY OF THE INVENTION The present invention provides a method for combining elemental boron or a boron compound, preferably boron carbide (B 4 C), with a carbonaceous feedstock other than premium petroleum coke, preferably anthracite, in an otherwise conventional electrode manufacturing process.
The process consists in transforming the highly disordered structure of anthracite into a highly graphitic structure. DETAILED DESCRIPTION OF THE INVENTION In the practice of this invention, particles of a non-petroleum coke carbonaceous feedstock are mixed with conventional pitch binders and lubricants, and elemental boron or boron-containing compounds are added to the mixture. Suitable carbonaceous feedstocks other than anthracite are bituminous coal, lignite and No. 2 and No. 3 coke. Preferably, the boron feedstock does not release gaseous by-products when reacting with the carbonaceous feedstock during the graphitization step during the manufacturing process. Such boron raw materials include elemental boron, boron carbide (B 4 C),
Silicon tetraboride ( B4Si ) and iron boride (FeB)
It is. The boron material can also be combined with the carbonaceous feedstock during calcination, in which
The boron compound can be an oxide such as boric acid (H 3 BO 3 ) or boron oxide (B 2 O 3 ).
This is because the gaseous by-products generated in this case do not affect the structural integrity of the finished electrode. Example A coarse anthracite electrode with a diameter of 6 inches was prepared by extrusion. Anthracite is heated to 2200℃ prior to crushing and sizing.
I roasted it. B 4 C additives for powdered coal, pitch, lubricants, and mixes are shown in the table below. The control mix contained no boron, while the mix of the boronated sample pieces was formulated to yield a finished product with about 3% boron by weight.
【表】
B4Cはカーボランダムカンパニ、テクニカルグ
レード325/Fであつて、72%のホウ素を含有し、
最大粒径44μmであつた。B4Cと粉炭は、加熱さ
れたシグマ羽根型ミキサの中で他の添加剤と混合
する前に、リボンブレンダーの中で1時間配合さ
れた。158℃のミツクス温度が得られた。次にこ
のミツクスを110℃まで冷却し、105℃で押出し
た。押出圧は、対照の場合390〜500psi、ホウ素
化ミツクスの場合400〜800psiの範囲であつた。
ホウ素含有ミツクスの押出し圧が高いことは、存
在結合剤が不十分であつたことを示し、これはお
そらくは物理的特性、特に強度に対して有害であ
ろうと思われる。しかしそれにもかかわらず、表
に表示の様に、ホウ素化電極は対照電極よりも
はるかに高い強度を有していた。各ミツクスか
ら、6インチ径×18インチ長のサイズの8個のビ
レツトを形成した。
これらのビレツトをサツガーの中にコークスパ
ツキングと共に包装し、2℃/時づつ500℃まで、
次に10℃/時づつ900℃まで焼成し、後者の温度
に約10時間保持した。
焼成されたビレツトをアツシユランド240石油
ピツチで含浸した。この含浸工程は、ビレツトを
オートクレーブ中に225℃まで予熱し、次にこの
チヤンバを半時間〜1時間、真空排気する段階を
必要とした。ピツチを250℃に加熱して導入し、
このシステムを100psiに加圧した。含浸されたビ
レツトをコークスパツキングの中に包装し、10
℃/時づつ750℃まで再焼成し、後者の温度に24
時間保持した。
黒鉛化工程は200℃/時の速度で2000℃まで、
次に400℃/時の速度で3000℃まで誘電加熱する
にあつた。3000℃での保持時間は1時間であつ
た。黒鉛化と冷却中に、コークスパツキングによ
つてストツクの酸化を防止した。
対照試料片とホウ素化無煙炭試料片とについて
得られた特性を表に示す。CTE以外のすべて
の特性は押出方向(WG)と押出方向に対して直
角(AG)とに切断された1″×1″×6″試料片につ
いて測定された。これらのデータは、9AG試料
片と11WG試料片との平均である。CTEデータは
本質的に室温値であり、またこれらの測定は
0.25″×0.75″×6″バーについて実施された。[Table] B 4 C is Carborundum Company, technical grade 325/F, containing 72% boron,
The maximum particle size was 44 μm. The B 4 C and powdered coal were blended in a ribbon blender for 1 hour before being mixed with other additives in a heated Sigma vane mixer. A mix temperature of 158°C was obtained. The mix was then cooled to 110°C and extruded at 105°C. Extrusion pressures ranged from 390-500 psi for controls and 400-800 psi for boronated mixes.
The high extrusion pressure of the boron-containing mix indicates that insufficient binder was present, which would likely be detrimental to the physical properties, especially strength. But nevertheless, as shown in the table, the borated electrode had much higher strength than the control electrode. Eight billets were formed from each mix, measuring 6 inches in diameter by 18 inches in length. These billets were packaged in a sugar bag with coke packing and heated at 2°C/hour up to 500°C.
It was then fired at 10°C/hour to 900°C and held at the latter temperature for about 10 hours. The fired billet was impregnated with Assuland 240 petroleum pitch. The impregnation process required preheating the billet in an autoclave to 225 DEG C. and then evacuating the chamber for one-half to one hour. Heat the pitch to 250℃ and introduce it.
The system was pressurized to 100 psi. Pack the impregnated billet in coke packing and
Refire to 750°C at 24°C/hour and to the latter temperature 24°C
Holds time. The graphitization process is carried out at a rate of 200℃/hour up to 2000℃,
Next, it was dielectrically heated to 3000°C at a rate of 400°C/hour. The holding time at 3000°C was 1 hour. During graphitization and cooling, stock oxidation was prevented by coke packing. The properties obtained for the control specimen and the borated anthracite specimen are shown in the table. All properties except CTE were measured on 1″ x 1″ x 6″ specimens cut in the extrusion direction (WG) and perpendicular to the extrusion direction (AG). These data are based on 9AG specimens. and an 11WG specimen.CTE data are essentially room temperature values, and these measurements are
Performed on 0.25″ x 0.75″ x 6″ bar.
【表】
化
[Table]
【表】
化
[Table]
Claims (1)
コークスからなる群から選ばれた炭素質物質を
カ焼すること、 (b) カ焼された炭素質物質を、石油ピツチ、潤滑
剤、及び元素ホウ素、炭化ホウ素、四ホウ化ケ
イ素とホウ化鉄からなる群から選ばれ、ホウ素
含有量が黒鉛電極の約0.1乃至約5.0重量%とな
るような量のホウ素源と混合して混合物をつく
ること、 (c) この混合物を電極の形に押出すこと、 (d) 前記電極の形を黒鉛化して黒鉛電極をつくる
こと を含むアーク炉黒鉛電極の製造方法。 2 ホウ素源が炭化ホウ素である特許請求の範囲
第1項記載の方法。 3 黒鉛電極のホウ素含有量は電極の約3.0重量
%である、特許請求の範囲第1項記載の方法。[Claims] 1 (a) Anthracite, bituminous coal, lignite, No. 2 and No. 3
(b) Calcining a carbonaceous material selected from the group consisting of coke; (c) extruding the mixture into the form of an electrode; and (c) extruding the mixture into an electrode. (d) A method for producing an arc furnace graphite electrode, comprising graphitizing the shape of the electrode to produce a graphite electrode. 2. The method according to claim 1, wherein the boron source is boron carbide. 3. The method of claim 1, wherein the boron content of the graphite electrode is about 3.0% by weight of the electrode.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US44309882A | 1982-11-19 | 1982-11-19 | |
US443098 | 1982-11-19 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59108294A JPS59108294A (en) | 1984-06-22 |
JPH0137839B2 true JPH0137839B2 (en) | 1989-08-09 |
Family
ID=23759400
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58217623A Granted JPS59108294A (en) | 1982-11-19 | 1983-11-18 | Carbon boride for electrode |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0109839B1 (en) |
JP (1) | JPS59108294A (en) |
DE (1) | DE3380551D1 (en) |
ES (1) | ES8407284A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1396948B1 (en) * | 2009-12-16 | 2012-12-20 | Italghisa S P A | ELECTRODIC PASTE FOR GRAPHITE ELECTRODES WITHOUT "BINDER" WITH HYDROCARBURIC BASIS |
CN105025602A (en) * | 2015-07-13 | 2015-11-04 | 河北联冠电极股份有限公司 | Carbon nanometer ultramicro material large carbon electrode and preparation method thereof |
JP6482442B2 (en) * | 2015-09-30 | 2019-03-13 | クアーズテック株式会社 | Carbon electrode for melting quartz glass |
DE102015221853B4 (en) | 2015-11-06 | 2019-05-16 | Technische Universität Bergakademie Freiberg | Process for the preparation of carbonaceous ceramic components |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1285559A (en) * | 1961-03-15 | 1962-02-23 | Union Carbide Corp | Production of artificial graphite |
DE1904408A1 (en) * | 1969-01-30 | 1970-08-06 | Conradty Fa C | High performance electrode with stabilized arc |
CH545249A (en) * | 1971-04-15 | 1973-12-15 | Lonza Ag | Process for making an isotropic graphite material |
DE3116258A1 (en) * | 1981-04-23 | 1982-11-11 | C. Conradty Nürnberg GmbH & Co KG, 8505 Röthenbach | ELECTRODE FOR ARC OVENS AND METHOD FOR USE THEREOF |
-
1983
- 1983-11-18 ES ES527373A patent/ES8407284A1/en not_active Expired
- 1983-11-18 EP EP19830307051 patent/EP0109839B1/en not_active Expired
- 1983-11-18 JP JP58217623A patent/JPS59108294A/en active Granted
- 1983-11-18 DE DE8383307051T patent/DE3380551D1/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
EP0109839B1 (en) | 1989-09-06 |
EP0109839A2 (en) | 1984-05-30 |
ES527373A0 (en) | 1984-08-16 |
EP0109839A3 (en) | 1985-06-19 |
DE3380551D1 (en) | 1989-10-12 |
ES8407284A1 (en) | 1984-08-16 |
JPS59108294A (en) | 1984-06-22 |
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