JPS59128209A - Method and apparatus for manufacturing calcium carbide - Google Patents
Method and apparatus for manufacturing calcium carbideInfo
- Publication number
- JPS59128209A JPS59128209A JP58000595A JP59583A JPS59128209A JP S59128209 A JPS59128209 A JP S59128209A JP 58000595 A JP58000595 A JP 58000595A JP 59583 A JP59583 A JP 59583A JP S59128209 A JPS59128209 A JP S59128209A
- Authority
- JP
- Japan
- Prior art keywords
- mixture
- cac2
- calcium carbide
- reaction
- combustion
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims abstract description 18
- 239000005997 Calcium carbide Substances 0.000 title claims description 26
- CLZWAWBPWVRRGI-UHFFFAOYSA-N tert-butyl 2-[2-[2-[2-[bis[2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl]amino]-5-bromophenoxy]ethoxy]-4-methyl-n-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl]anilino]acetate Chemical compound CC1=CC=C(N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)C(OCCOC=2C(=CC=C(Br)C=2)N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)=C1 CLZWAWBPWVRRGI-UHFFFAOYSA-N 0.000 title claims description 26
- 238000004519 manufacturing process Methods 0.000 title abstract description 8
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims abstract description 41
- 239000000292 calcium oxide Substances 0.000 claims abstract description 23
- 235000012255 calcium oxide Nutrition 0.000 claims abstract description 23
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 19
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 19
- 239000001301 oxygen Substances 0.000 claims abstract description 19
- 238000002485 combustion reaction Methods 0.000 claims abstract description 18
- 239000000203 mixture Substances 0.000 claims abstract description 13
- 239000000571 coke Substances 0.000 claims abstract description 11
- 239000003245 coal Substances 0.000 claims abstract description 9
- 238000010438 heat treatment Methods 0.000 claims abstract 4
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 16
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 15
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 5
- 229910002090 carbon oxide Inorganic materials 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 abstract description 21
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 12
- 229910052799 carbon Inorganic materials 0.000 abstract description 12
- 239000007789 gas Substances 0.000 abstract description 11
- 230000008018 melting Effects 0.000 abstract description 7
- 238000002844 melting Methods 0.000 abstract description 7
- 239000003575 carbonaceous material Substances 0.000 abstract description 5
- 238000005192 partition Methods 0.000 abstract description 4
- 239000000567 combustion gas Substances 0.000 abstract description 3
- 238000013021 overheating Methods 0.000 abstract description 3
- 239000012495 reaction gas Substances 0.000 abstract description 3
- 238000003860 storage Methods 0.000 abstract description 3
- 239000002893 slag Substances 0.000 abstract description 2
- 229910014813 CaC2 Inorganic materials 0.000 abstract 4
- 239000007858 starting material Substances 0.000 abstract 3
- 238000000354 decomposition reaction Methods 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 239000002994 raw material Substances 0.000 description 16
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 7
- RHZUVFJBSILHOK-UHFFFAOYSA-N anthracen-1-ylmethanolate Chemical compound C1=CC=C2C=C3C(C[O-])=CC=CC3=CC2=C1 RHZUVFJBSILHOK-UHFFFAOYSA-N 0.000 description 7
- 239000003830 anthracite Substances 0.000 description 7
- 239000002245 particle Substances 0.000 description 6
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 3
- 239000000374 eutectic mixture Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000002344 surface layer Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 238000006864 oxidative decomposition reaction Methods 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 229910002076 stabilized zirconia Inorganic materials 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 230000002747 voluntary effect Effects 0.000 description 1
Landscapes
- Carbon And Carbon Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
この発明は、電力によらず炭素と純酸素(空気中酸素で
ない酸素を言う、以下同じ)の燃焼熱を以ってカルシウ
ム・カーバイドを!!!造する方法(以後酸素法カルシ
ウム・カーバイド製造法造法と言う)及び装置の改良に
関するものである。[Detailed Description of the Invention] This invention produces calcium carbide using the combustion heat of carbon and pure oxygen (meaning oxygen that is not oxygen in the air, the same applies hereinafter) without relying on electricity! ! ! This paper relates to improvements in the method for producing calcium carbide (hereinafter referred to as the oxygen method for producing calcium carbide) and equipment.
酸素法カルシウム・カーバイド製造法は、熱誠として消
費された炭素と純酸素とか、化学工業原料として重要な
薗純反−酸化炭素として全量回収されるので、電力法に
比較して極めて有利であるため、従来多くの研究と提案
がなされて来たが、未だ工業的に実施されていない。そ
の理由は、従来のこの種の装置が、純酸素を直接に生石
灰と炭素質の混合物中に吹込んで、混合物中の炭素質を
直接酸素て燃焼せしめる方法を採っていたため、酸素吹
込み箇所に炭素の純酸素による完全燃焼が起こり、局部
的にr=度が数千0cに達し、酸化カ等の蒸発、熱分解
、酸化分解等が起こり、カルシウム・カーバイドの生成
が妨害され、且っ炉壁や酸素吹込管の溶融、損傷、更に
たい積原料が、燃焼と反応により空胴化した炉底部へ、
崩落する等の晶乱が起こり、安定した操業はほとんと不
可能であったためである。本発明は以上の諸欠陥を改善
するものである。以下に本発明の方法及び装置について
詳細に説明する。The oxygen method calcium carbide production method is extremely advantageous compared to the electric power method, as the carbon and pure oxygen consumed in the process of fervor are recovered in their entirety as pure anti-oxidized carbon, which is important as a raw material for the chemical industry. Although many studies and proposals have been made in the past, it has not yet been implemented industrially. The reason for this is that conventional equipment of this type injects pure oxygen directly into a mixture of quicklime and carbonaceous material, causing the carbonaceous material in the mixture to be directly combusted by the oxygen. Complete combustion of carbon with pure oxygen occurs, locally reaching r = several thousand degrees Celsius, evaporation of oxidizing power, thermal decomposition, oxidative decomposition, etc. occur, the formation of calcium carbide is hindered, and the furnace The walls and oxygen blowing pipes are melted and damaged, and the accumulated raw materials reach the bottom of the furnace, which has become a cavity due to combustion and reaction.
This was because crystal disturbances such as collapse occurred, making stable operation almost impossible. The present invention aims to improve the above-mentioned deficiencies. The method and apparatus of the present invention will be explained in detail below.
本発明方法の骨子は、粒子状の生石灰と石炭又はコーク
スの混合物が自然に安息角を保ってたい積している傾斜
面に、反応により発生する一酸化炭素と純酸素の燃焼炎
を投射し、該斜面の表層を加熱焼結してカルシウム・カ
ーバイド−上底の固4目反応を半ば起こさせ、継続して
供給される原料、の背圧により該表層をるつは内に滑落
せしめ、カルシウム・カーバイドと酸化カルシウムから
なる共融混合物内に投入し、固液用反応として反応を完
結せしめ、純度約80%前後の溶融カルシウム・カーバ
イドとして流出取得し、燃焼ガスは、炭素との反応によ
り再び一酸化炭素となり、カルシウム・カーバイド生成
の反応ガスと共に原料を予熱した後、その一部は再び酸
素との燃焼により反応に供される方法である。The gist of the method of the present invention is to project a combustion flame of carbon monoxide and pure oxygen generated by a reaction onto a slope where a mixture of particulate quicklime and coal or coke is piled up while maintaining a natural angle of repose. The surface layer of the slope is heated and sintered to partially cause the calcium carbide-upper solidification reaction, and the back pressure of the continuously supplied raw material causes the surface layer to slide down into the crucible.・Put it into a eutectic mixture consisting of carbide and calcium oxide, complete the reaction as a solid-liquid reaction, and obtain it as molten calcium carbide with a purity of about 80%.The combustion gas is regenerated by reaction with carbon. In this method, the raw material is preheated together with a reaction gas that turns into carbon monoxide and produces calcium carbide, and then a portion of the raw material is burned with oxygen again to be subjected to a reaction.
本発明方法によれば、熱源は一酸化炭素と純酸素の燃焼
炎によるために、炎の温度はバーナーの調節により酸素
の多少を以って精密な温度の調節が可能であるから、旧
来の方法におけるような極端な局部過熱による原料酸化
カルシウムや炭素の蒸発、昇華又は生成カルシウム・カ
ーバイドの熱分解等を引き起こすことはなく、又炉壁や
附属物等を溶融したり損傷したりすることもない。又、
酸素により生成カルシウム・カーバイドを酸化分解する
ことも防止出来る。又、本発明方法では、反応部と原料
予熱部とを明確に分離しているために、旧来の方′法の
ように予熱の目的で上部にたい積されている原料の圧力
により、下部の反応部が押しつぶされて崩落する等の混
乱は起こらない。According to the method of the present invention, since the heat source is a combustion flame of carbon monoxide and pure oxygen, the temperature of the flame can be precisely adjusted by adjusting the amount of oxygen by adjusting the burner. This method does not cause evaporation or sublimation of the raw calcium oxide or carbon or thermal decomposition of the produced calcium carbide due to extreme local overheating, and will not melt or damage the furnace walls or accessories. do not have. or,
Oxidative decomposition of calcium carbide produced by oxygen can also be prevented. In addition, in the method of the present invention, since the reaction section and the raw material preheating section are clearly separated, unlike the conventional method, the pressure of the raw material accumulated in the upper part for the purpose of preheating prevents the reaction in the lower part. There will be no confusion such as parts being crushed and collapsing.
又2000°C前後におけるカルシウム・カーバイド生
成反応は同相反応のため反応速度が極めてかさいが、本
発明方法では炭月と生石灰が加熱されて固4I4状態で
Hyε結1−ハt?’J融液上にdMし易い炭素質が生
石灰に固イど、された後、該傾斜面に背H―を加えて、
表層を、酸化カルシウムとりJルシウム・カーバイドの
共融混合物が1900〜2000’Cで溶融しているる
つば内に、滑落せしめ、残存酸化カルシウムをカルシウ
ム・カーバイドとの共融混合物として比較的低温で溶融
せしめ、炭素との反応を固液用反応として反応速度を増
大し、且つ発生する一酸化炭素を液中の気泡として反応
系外に出すことにより、カルシウム・カーバイド生成の
平衡をね利ならしめている。燃焼生成ガスは、炭酸ガス
と一酸化炭素の混合ガスとなるが、予熱部の1000〜
20(100Cの高温下に炭素と接触して全て一酸化炭
末となり、カルシウム・カーバイド生成反応により生成
する一酸化炭素と共に原料を(/熱して降θ、jXシ、
その一部はIJイび燃料として酸素による燃焼に供され
、残部は副産物として採取される。次に本発明方法及び
装置について図並びに実施例により具体的に説明する。In addition, the reaction rate of calcium carbide production at around 2000°C is extremely slow due to the in-phase reaction, but in the method of the present invention, the charcoal and quicklime are heated to form a solid 4I4 state with Hyε 1-hat? 'After the carbonaceous material that is easy to dM on the J melt is hardened into quicklime, a back H- is added to the slope,
The surface layer is slid down into a crucible in which a eutectic mixture of calcium oxide and lucium carbide is melted at 1900-2000'C, and the remaining calcium oxide is converted into a eutectic mixture with calcium carbide at a relatively low temperature. By melting and increasing the reaction rate by making the reaction with carbon a solid-liquid reaction, and by releasing the generated carbon monoxide out of the reaction system as bubbles in the liquid, the equilibrium of calcium carbide production is balanced. There is. The combustion generated gas is a mixed gas of carbon dioxide gas and carbon monoxide.
20 (contact with carbon at a high temperature of 100C, all becomes carbon monoxide powder, and the raw material is heated (/heated to reduce θ, jX,
A part of it is used for combustion with oxygen as IJ fuel, and the rest is collected as a by-product. Next, the method and apparatus of the present invention will be specifically explained with reference to figures and examples.
図は本発明方法及び装置を説明するための模式図である
。予め粉砕し粒度を一定にそろえた生石灰及び無煙炭又
はコークスの一定割合の均@混合物が原料貯そう1より
スクリュー・コンベアー2を以って一部量宛炉体3の上
部より予熱部4に供給され、目孔仕切板5の上方にたい
積され、燃焼室6よりの熱ガスに依って予熱されて、水
平開閉廊7の開度に従って一部量宛炉底8に送入され、
安息角傾斜面9を保ちつつ燃焼室6内に押出される。一
方ガスギ送機10により圧送される一1浚化炭紮は、混
合器11において、酸素供給管12より送入される純酸
素と混合され、燃焼器13で燃焼され、燃焼炎が原料傾
斜面9に投射される。傾斜面9の生石灰と無煙炭又はコ
ークス粒子は加熱され、固41」反応により生石灰粒子
と無煙炭又はコークス粒・子とが焼結し、法統原料の圧
力に押されて溶融るつば14内に滑落し、固簸相反応に
より反応が完結され、生成したカルシウム・カーバイド
約80%、生石灰約20%の溶融混合物はカルシウム・
カーバイド出口15より流出し、液面に浮上するスラッ
プはスラップ出口16より排出される。燃焼ガス及び1
1a′I斜iMi 9と浴融るつば14より発生する反
応ガスは、[」孔イ」切板5の1」孔より予熱¥4に入
り、ガス中の炭酸カスは、髄温下原料中の炭素に接触し
て一酸化炭素となり、原料を予熱して上部ガス出D 1
7より抽出され、その−gliは圧送機」0により混合
器11に送られて酸素と混合され゛、燃焼器]3により
燃焼され、再びカルシウム・カーバイド生成反応の熱隙
に供される。炉内において1900’C以」二に接し、
且つ強度を要する場所、RIJち目孔仕切板5、燃焼室
6、水平開閉卑7、炉底8、浴融るっば14、カルシウ
ム・カーバイド出O15、スラッグ出口16の拐質は酸
化カルシウム部分安定化ジルコニアとし、その他はその
温度に応じる1ljJ穴度のAA質を用いる。次に実施
例について説明する。The figure is a schematic diagram for explaining the method and apparatus of the present invention. A homogeneous mixture of quicklime and anthracite or coke in a fixed proportion, which has been crushed in advance and has a uniform particle size, is supplied from the raw material storage 1 to the preheating section 4 from the upper part of the furnace body 3 via a screw conveyor 2. is piled up above the perforated partition plate 5, preheated by hot gas from the combustion chamber 6, and fed into the hearth bottom 8 in portions according to the opening degree of the horizontal opening/closing corridor 7.
It is pushed out into the combustion chamber 6 while maintaining the angle of repose inclined surface 9. On the other hand, the dredged carbon silica fed under pressure by the gas feeder 10 is mixed with pure oxygen fed from the oxygen supply pipe 12 in the mixer 11, and is combusted in the combustor 13, so that the combustion flame is spread over the slope of the raw material. Projected to 9. The quicklime and anthracite coal or coke particles on the inclined surface 9 are heated, and the quicklime particles and the anthracite coal or coke particles are sintered by a solid reaction, and pushed by the pressure of the raw material, they slide down into the molten collar 14. The reaction is completed by a solid elutriation phase reaction, and the resulting molten mixture of about 80% calcium carbide and about 20% quicklime is calcium carbide.
Slap that flows out from the carbide outlet 15 and floats to the liquid surface is discharged from the slap outlet 16. combustion gas and 1
The reaction gas generated from the 1a'I diagonal iMi 9 and the bath melting collar 14 enters the preheated ¥4 through the 1'' hole of the cutting plate 5, and the carbon dioxide in the gas is absorbed into the raw material under marrow temperature. It comes into contact with carbon and becomes carbon monoxide, which preheats the raw material and releases upper gas
7, the -gli is sent to a mixer 11 by a pressure feeder 0, mixed with oxygen, combusted in a combustor 3, and again provided to the heat gap for the calcium carbide production reaction. 1900'C or higher in the furnace,
In places where strength is required, RIJ perforated partition plate 5, combustion chamber 6, horizontal opening/closing base 7, furnace bottom 8, bath melting chamber 14, calcium carbide outlet O 15, and slag outlet 16, the particulate matter is calcium oxide. Stabilized zirconia is used, and the rest is made of AA material with a hole size of 1ljJ depending on the temperature. Next, an example will be described.
純+W約80%のカルシウム・カーバイド日ノμ−lト
ンの本発明方法の実験装置による実施例を示せば次の如
し。平均粒径1oおの生石灰1正損と同粒径の無煙炭1
.94重量の均一混合物毎時114.5に9を原眉貯#
]より供給し、前記の装置の説明の通り操作して原料傾
斜面9を型成させ、一方ガス圧送機10より圧送される
毎時s5.xN、、zの一酸化炭素を、管12より圧送
される毎時42.5Niの純酸累を以って燃規至6内で
燃焼せしめ、発生ずる炎を該傾斜面に投射し、以後前記
説明の通りに操作した結果、カルシウム・カーバイド出
口15より岳時41.7Kgの82%純度のカルシウム
・カー八イドが得られ、上部ガス出口17より98%純
度で釣200°Cの一酸化炭素毎時182.3Nm3が
排出され、その回毎時85..lN77%が反応用熱誠
として酸素と燃焼に供され、残り毎時97.2N、IF
の98%純反の一酸化炭素が副産物として得られた。An example of the method of the present invention using an experimental apparatus for preparing approximately 80% pure +W calcium carbide is as follows. 1 piece of quicklime with average particle size 1 piece of anthracite with the same particle size
.. Uniform mixture of 94 weight per hour 9 to 114.5 #
] and operated as described above to form the raw material inclined surface 9, while the hourly s5. The carbon monoxide xN,,z is combusted in the fuel standard 6 using 42.5Ni per hour of pure acid pumped through the pipe 12, and the flame generated is projected onto the slope. As a result of operating as described, 41.7 kg of calcium carbide with 82% purity was obtained from the calcium carbide outlet 15, and 98% pure calcium carbide was obtained from the upper gas outlet 17 at 200°C with carbon monoxide. 182.3 Nm3 was emitted per hour, and 85.3 Nm3 per hour was emitted. .. 77% of lN is used for combustion with oxygen as reaction heat, remaining 97.2N/hour, IF
98% pure carbon monoxide was obtained as a by-product.
以上を82%純度のカルシウム・カーバイド1トン当り
の原単位に換算すると、生石灰935.3に9、無煙炭
1810.51’:9、酸]1o2o、5Niを消費し
、2332.1Nデの一酸化炭素を副産することとなり
、これを従来方法のIQ Q位、82%カルシウム・カ
ーバイド1トン当り、生石灰1000Kg、無煙炭2Q
OOK9、酸素1100N771!を消費し、230o
Nm3の一酸化炭素を発生するのに比較して効率がはる
かに商いことが認められ、なお且つ本実験は局部過熱に
よる前述のような混乱もなく長期間安定した操業が得ら
れた。Converting the above to the consumption per ton of calcium carbide with 82% purity, 935.3 to 9 of quicklime, 9 to 1810.51' of anthracite, 5 Ni of acid] are consumed, and monoxide of 2332.1N of Carbon is produced as a by-product, and this is compared to the IQ of the conventional method, per 1 ton of 82% calcium carbide, 1000 kg of quicklime, and 2 Q of anthracite.
OOK9, oxygen 1100N771! consumes 230o
It was recognized that the efficiency was much higher than that of generating Nm3 carbon monoxide, and in addition, stable operation for a long period of time was obtained in this experiment without the above-mentioned disturbance due to local overheating.
なお炭材として無煙炭の替りにコークスを用いることも
出来ることは論を待たない。It goes without saying that coke can be used instead of anthracite as the carbon material.
図は本発明方法及び装置を説明するための模式図であっ
て、lは原料貯槽、2はスクリュー・コンベアー、3は
炉体、4は予熱部、5は目孔仕切板、6は燃焼室、7は
水平開閉涛、8は炉底、9は原料安息角傾斜面、10は
ガス圧送機、11は程合器、12は酸素供給管、13は
燃焼器、14は浴融るつは、15はカルシウム・カーバ
イド出口、6はスラッグ出口、17はガス出口をそれぞ
れ示す。
手 続 補 正 書(自発)
q守Wl’lf J*官苔杉和夫殿
1.41件の表74< 昭和58年特許出願第000
595匂2、発明の名利、 ノコルシウム・カーバイド
を製造する方法及び装置
3・補正する名゛
住所 新潟市小金町15番地
明細書
5、補正の内容The figure is a schematic diagram for explaining the method and apparatus of the present invention, where l is a raw material storage tank, 2 is a screw conveyor, 3 is a furnace body, 4 is a preheating section, 5 is a hole partition plate, and 6 is a combustion chamber. , 7 is a horizontal opening/closing valve, 8 is a furnace bottom, 9 is a slope of the angle of repose of the raw material, 10 is a gas pumper, 11 is a tempering vessel, 12 is an oxygen supply pipe, 13 is a combustor, 14 is a bath melting unit, 15 indicates a calcium carbide outlet, 6 indicates a slug outlet, and 17 indicates a gas outlet. Procedural Amendment (Voluntary) qkori Wl'lf J*Kankokesugi Kazuo 1.41 Table of 74< 1981 Patent Application No. 000
595 No. 2, Benefits of the invention, Method and apparatus for producing nocolsium carbide 3. Name and address to be amended: 15 Koganemachi, Niigata City Specification 5, Contents of amendment
Claims (3)
と酸素の燃焼炎により加熱してjjルシウム・カーバイ
ドと一酸化炭素を製造する方法。(1) A method of producing lucium carbide and carbon monoxide by heating a mixture of quicklime and coal or coke with a combustion flame of carbon monoxide and oxygen.
と酸素の燃焼炎を以って加熱してカルシウム・カーバイ
ドと一酸化炭素を造り、該−酸化炭素が生石灰と石炭又
はコークスを予熱した後、その一部が再び酸素により燃
焼して生石灰と石炭又はコークスの混合物を加熱するこ
とを特徴とする、カルシウム・カーバイドを製造する装
置。(2) heating a mixture of quicklime and coal or coke with a combustion flame of carbon monoxide and oxygen to produce calcium carbide and carbon monoxide, after the carbon oxide preheats the quicklime and coal or coke; An apparatus for producing calcium carbide, characterized in that a part of it is burned again with oxygen to heat a mixture of quicklime and coal or coke.
然たい積せしめ、安息角を保って形成落せしめて浴融す
ることを特徴とする特、ヂ1゜請求範囲(2)の装置。(3) The apparatus according to claim (2), characterized in that a mixture of particulate quicklime and coal or coke is naturally deposited, formed while maintaining an angle of repose, and melted in a bath.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58000595A JPS59128209A (en) | 1983-01-05 | 1983-01-05 | Method and apparatus for manufacturing calcium carbide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58000595A JPS59128209A (en) | 1983-01-05 | 1983-01-05 | Method and apparatus for manufacturing calcium carbide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS59128209A true JPS59128209A (en) | 1984-07-24 |
Family
ID=11478086
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58000595A Pending JPS59128209A (en) | 1983-01-05 | 1983-01-05 | Method and apparatus for manufacturing calcium carbide |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59128209A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4683621A (en) * | 1984-10-02 | 1987-08-04 | Nippon Notion Kogyo Co., Ltd. | Flexible button |
| JP2011529840A (en) * | 2008-08-01 | 2011-12-15 | 北京化工大学 | Carbide manufacturing method and system |
| CN105293495A (en) * | 2015-11-04 | 2016-02-03 | 中冶南方工程技术有限公司 | Flash smelting furnace for calcium carbide and system |
| CN106564900A (en) * | 2016-11-07 | 2017-04-19 | 中国石油大学(华东) | Clean, efficient and safe process for preparing calcium carbide powder through molten-state calcium carbide cooling |
| CN108502884A (en) * | 2018-03-23 | 2018-09-07 | 宁夏宝塔化工中心实验室(有限公司) | A method of producing the grey mix and convert calcium lime powder pressure ball molding of calcium carbide furnace of calcium carbide purification |
-
1983
- 1983-01-05 JP JP58000595A patent/JPS59128209A/en active Pending
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4683621A (en) * | 1984-10-02 | 1987-08-04 | Nippon Notion Kogyo Co., Ltd. | Flexible button |
| JP2011529840A (en) * | 2008-08-01 | 2011-12-15 | 北京化工大学 | Carbide manufacturing method and system |
| CN105293495A (en) * | 2015-11-04 | 2016-02-03 | 中冶南方工程技术有限公司 | Flash smelting furnace for calcium carbide and system |
| CN106564900A (en) * | 2016-11-07 | 2017-04-19 | 中国石油大学(华东) | Clean, efficient and safe process for preparing calcium carbide powder through molten-state calcium carbide cooling |
| CN106564900B (en) * | 2016-11-07 | 2019-03-29 | 中国石油大学(华东) | A kind of cooling calcium carbide powder technique processed of the molten state calcium carbide of clean and effective safety |
| CN108502884A (en) * | 2018-03-23 | 2018-09-07 | 宁夏宝塔化工中心实验室(有限公司) | A method of producing the grey mix and convert calcium lime powder pressure ball molding of calcium carbide furnace of calcium carbide purification |
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