JPS6042465A - Production of acetylene black - Google Patents

Production of acetylene black

Info

Publication number
JPS6042465A
JPS6042465A JP14999883A JP14999883A JPS6042465A JP S6042465 A JPS6042465 A JP S6042465A JP 14999883 A JP14999883 A JP 14999883A JP 14999883 A JP14999883 A JP 14999883A JP S6042465 A JPS6042465 A JP S6042465A
Authority
JP
Japan
Prior art keywords
section
aging
acetylene
thermal decomposition
carbon
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
Application number
JP14999883A
Other languages
Japanese (ja)
Inventor
Mitsuo Nakakawara
中河原 三雄
Eizo Mori
森 英蔵
Kunio Sugano
菅野 国夫
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Denka Co Ltd
Original Assignee
Denki Kagaku Kogyo KK
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 Denki Kagaku Kogyo KK filed Critical Denki Kagaku Kogyo KK
Priority to JP14999883A priority Critical patent/JPS6042465A/en
Publication of JPS6042465A publication Critical patent/JPS6042465A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To produce acetylene black having good hydrochloric acid absorption consistently over a long period of time, by using a thermal cracker having a thermal cracking part and an aging part in series and treating acetylene gas under specified conditions. CONSTITUTION:A vertical tubular cracker composed of a thermal cracking part 1 and an aging part 2 and satisfying the relationship of D1/D2=1.2-2.2 and L1/L2=0.4-1, wherein D1 is the diameter of the thermal cracking part 1 and L1 is the length thereof, and D2 is the diameter of the aging part 2 and L2 is the length thereof, is used. Acetylene gas [which may contain not more than 40wt% (in terms of carbon) unsaturated hydrocarbons such as propylene and benzene] is thermally cracked at 1,900 deg.C and cracked products contg. carbon aerosol are allowed to stay for 30-150sec. in the thermal cracking part 1. The formed aerosol is allowed to stay at 1,700 deg.C or above for 20-90sec to produce acetylene black in the aging part 2.

Description

【発明の詳細な説明】 本発明はアセチレンブランクの製造方法、さらに詳しく
説明すると、14品の塩酸吸液量を低下させることなく
長期操業可能なアセチレンブランクの製造方法に関する
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing an acetylene blank, and more specifically, to a method for producing an acetylene blank that can be operated for a long period of time without reducing the hydrochloric acid absorption of 14 products.

従来アセチレンブランクの製造方法、としては、アセチ
レンガスを熱分解し、その時発生する分解熱により引続
き連続的に供給されるアセチレンガスを分解させて必要
な温度を几持シつつ、連続してアセチレンブラックta
造する方法が知られている(便覧カーがンブランク昭和
25年9月版)。しかし、この公知の方法でアセテレン
プ2ンクti+li造する場合、生成したアセチレンブ
ラックが炉内の内壁面に附着するために、製品の塩酸吸
液量の低下や分解炉の閉塞などが起り、品質の良好なア
セチレンブラックを長期操業して製造することができな
い欠点があった。
Conventional methods for producing acetylene blanks include thermally decomposing acetylene gas, decomposing the continuously supplied acetylene gas using the decomposition heat generated at that time, and continuously producing acetylene black while maintaining the required temperature. ta
There is a known method for making it (Handbook Car Gun Blank September 1950 edition). However, when acetylene black is produced using this known method, the produced acetylene black adheres to the inner wall surface of the furnace, resulting in a decrease in the amount of hydrochloric acid absorbed by the product and clogging of the decomposition furnace, resulting in poor quality. The drawback was that it was not possible to produce good acetylene black over a long period of time.

本発明はアセチレンガスA又はアセチレンガスAに不飽
和炭化水素Bを前記A中の炭素分100重量部に対しB
中の炭素分が40重量部以下となるように添加した原料
を、熱分解部1と熟成部2とからなり、しかも熟成部2
の直径D2に対する熱分解部1の直径D1の比CDI/
D2)が1.2〜2.2、かつ熟成部2の長さり、に対
する熱分解部1の長さり。
The present invention is characterized in that acetylene gas A or unsaturated hydrocarbon B is added to acetylene gas A per 100 parts by weight of carbon in said A.
The raw material added so that the carbon content is 40 parts by weight or less is processed into a thermal decomposition section 1 and a ripening section 2.
The ratio of the diameter D1 of the pyrolysis section 1 to the diameter D2 of CDI/
D2) is 1.2 to 2.2, and the length of the thermal decomposition section 1 is relative to the length of the aging section 2.

の比LLI/L2)が6.4〜1.0である竪型円筒状
分解炉に供給し、熱分解してアセチレンブランクを製造
するにあたり、前記熱分Wr部1および熟成部2を下記
の条件で操作することを特徴とするアセチレンブランク
の製造方法である。
When supplying to a vertical cylindrical cracking furnace with a ratio LLI/L2) of 6.4 to 1.0 and thermally decomposing it to produce an acetylene blank, the heat Wr part 1 and the aging part 2 were This is a method for producing an acetylene blank characterized by operating under certain conditions.

熱分解部1:温度1900℃以上の分解生成物の雰囲気
に該分解生成物中 のカーボンエアロゾルを標4 状態換算で30〜150秒n1? 溜させる。
Thermal decomposition section 1: The carbon aerosol in the decomposition product is placed in the atmosphere of the decomposition product at a temperature of 1900°C or higher for 30 to 150 seconds n1? Let it accumulate.

熟成部2:熱分解部から導入された温度1700℃以上
のカーボンエア ロゾルを標準状態換算で20 〜90放滞溜させる。
Aging section 2: The carbon aerosol introduced from the thermal decomposition section and having a temperature of 1,700°C or higher is allowed to accumulate for 20 to 90 hours in terms of standard conditions.

以下本発明の内容を詳細に説明する。The contents of the present invention will be explained in detail below.

本発明において使用する原料としては、アセチレンガス
A又はアセチレンガスAにエチレン系、単項式、多環式
、及び芳香族系の不飽和炭化水素から選ばれた一種以上
を添加したものが使用できるが、必ずしもこれらに限ら
れるものではない。
As the raw material used in the present invention, acetylene gas A or acetylene gas A to which one or more selected from ethylene, monomial, polycyclic, and aromatic unsaturated hydrocarbons can be used. It is not necessarily limited to these.

エチレン系不飽和炭化水素の具体例としては、エチレン
、プロピレン及びブクノエン等、又多環式不飽和炭化水
素の具体例としてはベンゼン、フレオン−1・油、ナフ
タレン等が企げられる。
Specific examples of ethylenically unsaturated hydrocarbons include ethylene, propylene, buknoene, etc., and specific examples of polycyclic unsaturated hydrocarbons include benzene, freon-1 oil, naphthalene, and the like.

上記した不飽和炭化水素Bの選択にあたつては、熱分解
炉の構造、原料の分解熱及び操作方法等によって決定す
るが、アセチレンガスに対する添加割合は、アセチレン
ガスA中゛の炭素分100重量部に対し上記不飽和炭化
水素B中の炭素分が40重量部以下となるようにするこ
とが好ましい。
The selection of the unsaturated hydrocarbon B described above is determined by the structure of the pyrolysis furnace, the decomposition heat of the raw material, the operating method, etc., but the addition ratio to the acetylene gas is determined by the carbon content in the acetylene gas A being 100 It is preferable that the carbon content in the unsaturated hydrocarbon B is 40 parts by weight or less relative to parts by weight.

不飽和炭化水素Bの割合が40重量部をこえると、連続
して原料を熱分解させるための温度を維持することがで
きなくなるために、製品アセチレンブラックの塩酸吸液
量が低下するので好ましくない。次に不飽和炭化水素B
’5アセチレンガスに混合するときは前記炭化水素Bを
気化器で気化させた後7行なえばよい。
If the proportion of unsaturated hydrocarbon B exceeds 40 parts by weight, it is not possible to maintain the temperature for continuous thermal decomposition of the raw material, so the amount of hydrochloric acid absorbed by the product acetylene black decreases, which is undesirable. . Next, unsaturated hydrocarbon B
When mixing with '5 acetylene gas, it is sufficient to vaporize the hydrocarbon B in a vaporizer and then carry out 7 steps.

以上説明した原料を第1図に示すような堅型円筒状炉に
供給する。この炉は熱分解部1と熟成部2とからなり、
しかも熟成部2の直径D2に対する熱分解部1の直径D
Iの比(D、/D2)が1.2〜2.2、好捷しくは1
.3〜1.8であり、しかも熟成部2の長さL2に対す
る熱分解部1の長さり、の比(L +/ L 2)が0
4〜1.0、好ましくは06〜0.8である形状に構成
されていることが好ましい。すなわち従来の方法におい
て用いる熱分解炉は、熱分解部と熟成部の区分がなく、
熱分解部と熟成部が操業条件によって複雑多岐に入り交
るため、品質の安定をかき量産出来ないのに対し、本発
明は熱分解部と熟成部を明確に区分され各々独立して存
在させるようにした炉を用いることにより、品質の安定
及び量産を可能とするものである。
The raw materials explained above are fed to a vertical cylindrical furnace as shown in FIG. This furnace consists of a pyrolysis section 1 and a ripening section 2,
Moreover, the diameter D of the thermal decomposition section 1 is relative to the diameter D2 of the aging section 2.
The ratio of I (D, /D2) is 1.2 to 2.2, preferably 1
.. 3 to 1.8, and the ratio (L + / L 2) of the length of the thermal decomposition section 1 to the length L2 of the aging section 2 is 0.
It is preferable to have a shape of 4 to 1.0, preferably 06 to 0.8. In other words, the pyrolysis furnace used in the conventional method does not have a pyrolysis section and a ripening section;
The thermal decomposition section and the ripening section are complicated and intertwined depending on the operating conditions, making it difficult to maintain quality and mass production.However, in the present invention, the thermal decomposition section and the ripening section are clearly separated and exist independently. By using such a furnace, stable quality and mass production are possible.

すなわち本発明において用いる熱分解炉の場合は、熱分
解部1においては熱分解反応を均一にするため必要な温
度を保ちながら、その雰囲気に所定時間滞溜させて熱分
1yf反応を完結させると共に連鎖構造を発達させたも
のとする(以下カーがンエアロゾルという)。
In other words, in the case of the pyrolysis furnace used in the present invention, in the pyrolysis section 1, while maintaining the necessary temperature to make the pyrolysis reaction uniform, the heat component 1yf reaction is completed by staying in the atmosphere for a predetermined time. It is assumed that a chain structure has developed (hereinafter referred to as a carbon aerosol).

次いでこれを熟成部2において、熱分解反応によって発
生した熱により分子配列が整えられ、連鎖構造が強化さ
れるに必要な時間滞溜させることにより、製品の塩酸吸
液量の低下させることなく、炉の閉塞が防止され長期操
業力ゞ可能となる。
Next, in the aging section 2, the heat generated by the thermal decomposition reaction adjusts the molecular arrangement and allows the product to remain for a time necessary to strengthen the chain structure, without reducing the amount of hydrochloric acid absorbed by the product. Blockage of the furnace is prevented and long-term operating power is possible.

本発明において用いる炉については、上記範囲以外の形
状である場合には本発明の目的を達成することが難しい
Regarding the furnace used in the present invention, if the shape is outside the above range, it will be difficult to achieve the purpose of the present invention.

以上説明した分解炉に供給された原料は、1ず熱分解部
1で1900℃以上の温度で熱分解され、カーボンエア
ロゾルを含有した分解生成物を生成する。
The raw material supplied to the decomposition furnace described above is first thermally decomposed at a temperature of 1900° C. or higher in the thermal decomposition section 1 to generate a decomposition product containing carbon aerosol.

ここで必要なことは、この熱分解部1で上記エアロゾル
を含有した分解生成物を所定時間滞溜させることである
が、その条件は1900℃以上の温度でしかも標準状態
換算で30〜150秒滞溜させることである。滞溜させ
る熱分解部1の温度が1900℃未満では原料の熱分解
反応が完結せず、連鎖構造が発達しない。
What is required here is to allow the decomposition products containing the aerosol to remain in the thermal decomposition section 1 for a predetermined period of time, and the conditions for this are a temperature of 1900°C or higher and a time period of 30 to 150 seconds in terms of standard conditions. It is to let it accumulate. If the temperature of the thermal decomposition section 1 where the material is stored is lower than 1900° C., the thermal decomposition reaction of the raw material will not be completed and a chain structure will not develop.

1だ、滞溜時間が30秒未満では製品の連鎖構造が発達
しないし、150秒をこえると生成アセチレンブラック
の2次粒子の凝集化が起る。
1. If the residence time is less than 30 seconds, the chain structure of the product will not develop, and if it exceeds 150 seconds, the secondary particles of the acetylene black produced will aggregate.

滞溜時間の調節は原料の供給量を変えることによジ行わ
れる。原料ガス線速度は標準状態換算で0.01〜0.
06m/秒、好ましくは002〜0.05m/秒が適当
である。
The residence time is adjusted by changing the feed rate of the raw material. The raw material gas linear velocity is 0.01 to 0.0 in terms of standard conditions.
0.6 m/sec, preferably 0.02 to 0.05 m/sec is suitable.

次に熱分解部1で生成したカーボンエアロゾル含有熱分
解生成物を熟成部2に導入する。
Next, the carbon aerosol-containing pyrolysis product produced in the pyrolysis section 1 is introduced into the aging section 2.

熟成部2では前記カー−?ンエアロゾルの改質が行われ
るが、その条件としては、1700℃以上の温度でしか
も20〜90秒滞溜させることが好ましい。
In the aging section 2, the car? The aerosol is modified, and the conditions are preferably that it is kept at a temperature of 1700° C. or higher and for 20 to 90 seconds.

温度が1700℃未満では分解生成物中のカーytfン
エアロゾルの分子配列を整えることができないため製品
の塩酸吸液量が低下するので、好ましくない。
If the temperature is less than 1700° C., the molecular arrangement of carbon ytf aerosol in the decomposition product cannot be adjusted, so the amount of hydrochloric acid absorbed by the product decreases, which is not preferable.

また滞溜時間が20秒未満ではカーボンエアロゾルの分
子配列を整えて改質することができないし、90秒をこ
えるとカーボンエアロゾルの2次粒子の凝集化が促進さ
れると共に炉壁への町着が多くなるので好ましくない。
Furthermore, if the residence time is less than 20 seconds, the molecular arrangement of the carbon aerosol cannot be adjusted and reformed, and if the residence time exceeds 90 seconds, the agglomeration of the secondary particles of the carbon aerosol will be promoted and the particles will accumulate on the furnace wall. This is not preferable as it increases the number of

この場合のガス線速度は標準状態換算で0.03〜(1
,14m7秒 、好ましくは0.05−Q、 、L l
 m7秒 と熱分j’l’1都のそれよりガスの流速を
速める事によp熱分解部で生成されたアセチレンブラン
クの熟成をそこなうことなく炉壁へのアセチレンブラン
クの防着を防ぐことができる。
In this case, the gas linear velocity is 0.03 to (1
, 14m7 seconds, preferably 0.05-Q, , L l
To prevent the acetylene blank from adhering to the furnace wall without impairing the ripening of the acetylene blank produced in the p-pyrolysis section by increasing the gas flow rate from that of m7 seconds and heat fraction j'l'1. Can be done.

以上説明したように、本発明の方法は原料ガスを特定の
形状の熱分解炉に供給し熱分91部1で生成したカーボ
ンエアロゾルを熟成部2で改質することによる効果と長
期操業を可能とする生産性の効果とを併せて達成するも
のであり、従来品より塩酸吸液量が1.0〜1.3CC
15g高いアセチレンブランクラ1.2〜1.4倍多量
に生産することができる。
As explained above, the method of the present invention enables effects and long-term operation by supplying the raw material gas to a pyrolysis furnace with a specific shape and reforming the carbon aerosol produced in the heat component 91 part 1 in the aging part 2. This product also achieves the productivity effects of 1.0 to 1.3 cc of hydrochloric acid compared to conventional products.
It is possible to produce 1.2 to 1.4 times more acetylene blank, which is 15g higher.

次に本発明を実施例をあげて説明する。Next, the present invention will be explained by giving examples.

実施例1および比較例1 第1図に示す構造の熱分解炉の熱分w1部1の直径D1
が74cm5その長さLlが250m1熟成部2の直径
D2が50crn1その長さL2が360crnである
竪型円筒状分解炉+ DI/D2= 1.48、”l/
L2= 0.69 )にアセチレンガスを50 N”/
fi、”間供給し−Cアセチレンブランク全製造した。
Example 1 and Comparative Example 1 Diameter D1 of heat component w1 part 1 of a pyrolysis furnace having the structure shown in FIG.
is 74 cm5, its length Ll is 250 m1, the diameter D2 of the ripening section 2 is 50 crn1, its length L2 is 360 crn + DI/D2 = 1.48, "l/
L2=0.69) with acetylene gas at 50 N”/
Acetylene blanks were completely produced by supplying them for a period of time.

捷た比較のために熱分91部と熟成部とを区別のない寸
胴の第2図に示す構造の直径50crnの熱分解炉にア
セチレンガス40 ”/時間を供給してアセチシブ5r
ノ、lt=製造した。これらの条件および結果を第1表
に示す。
For comparison purposes, 91 parts of the heat and the aging section were fed into a pyrolysis furnace with a diameter of 50 crn as shown in Fig. 2 with no distinction between the two, and acetylene gas was supplied at 40''/hour to produce 5r of acetylene gas.
ノ,lt=manufactured. These conditions and results are shown in Table 1.

実施例2および比較例2 実施例1で用いた分解炉にアセチレンガス58N7″゛
/時間に温度]、 l 0℃に加熱して気化したベンゼ
ン21”時間を添加した原料を供給した以外は実施例1
と同様に行った。
Example 2 and Comparative Example 2 The same procedure was carried out except that the same raw material was supplied to the decomposition furnace used in Example 1, with the addition of acetylene gas of 58N 7''/hour and benzene heated to 0°C and vaporized for 21 hours. Example 1
I did the same thing.

比較のために比較例1で用いた熱分解炉を用いた以外は
実施例2と同様に行った。
The same procedure as in Example 2 was conducted except that the pyrolysis furnace used in Comparative Example 1 was used for comparison.

比較例3 アセチレンガス2ON″”/時間’第2図に示す構造の
熱分解炉に供給したこと以外は実施例1と同様に行った
Comparative Example 3 The same procedure as in Example 1 was carried out except that acetylene gas was supplied to a thermal decomposition furnace having the structure shown in FIG. 2 at a rate of 2ON''/hour.

比較例4 アセチレンガス160−’jigz間に第2図の分解炉
に供給したこと以外は実施例1と同様に行った。
Comparative Example 4 The same procedure as in Example 1 was carried out except that acetylene gas was supplied to the decomposition furnace shown in FIG. 2 at a rate of 160 mm.

以上、実施例において示すように、本発明の方法によれ
ば、従来の場合にくらべ長期操業することにより塩酸吸
液量の高いアセチレンブラックを多量に生産することが
できる。
As shown in the Examples above, according to the method of the present invention, acetylene black with a high hydrochloric acid absorption capacity can be produced in large quantities by operating for a longer period than in the conventional case.

(注l) 第1表に記載した分解生成物の滞溜時間及び
ガス線速度の算出は次の 方法Vtよった。
(Note 1) The residence time and gas linear velocity of the decomposition products listed in Table 1 were calculated according to the following method Vt.

(注2) 塩酸吸液量の測定はJISK1469に準拠
して行った。(単位”75 g l(注3) 操業時間
はスタートから炉内閉塞に至るまでの時間で示した。
(Note 2) The amount of hydrochloric acid absorbed was measured in accordance with JIS K1469. (Unit: 75 g l (Note 3) The operating time is expressed as the time from start to blockage in the furnace.

(注4) 熱分解部1及び熟成部2の温度は炉内中心部
までグラッシーカーピン 製(東海カーがン製)保護管を入れ、 その先端温度を光高温計で測定した。
(Note 4) The temperatures in the pyrolysis section 1 and aging section 2 were determined by inserting a Glassy Carpin (manufactured by Tokai Cargan) protection tube to the center of the furnace, and measuring the temperature at the tip with an optical pyrometer.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の実施例に用いた竪型円筒状分解炉の説
明図、第2図は比較例に用いた熱分解炉の説明図である
。 何分 1・・・熱分解部 2・・・熟成部 特許出願人 電気化学工業株式会社
FIG. 1 is an explanatory diagram of a vertical cylindrical decomposition furnace used in an example of the present invention, and FIG. 2 is an explanatory diagram of a pyrolysis furnace used in a comparative example. What fraction 1...Pyrolysis section 2...Aging section Patent applicant Denki Kagaku Kogyo Co., Ltd.

Claims (1)

【特許請求の範囲】 アセチレンガスA又はアセチレンガスAに不飽和炭化水
素Bを前記A中の炭素分100重量部に対しB中の炭素
分が40重量部以下を含有させた原料を、熱分解部1と
熟成部2とからなり、しかも熟成部2の直径D2に対す
る熱分解部1の直径D+の比(D +/ D t)が1
.2〜22、かつ熟成部2の長さり、に対する熱分解部
1の長もり、の比LLs/Ltlが0.4〜1.0であ
る竪型円筒状分解炉に供給し、熱分解してアセナレノブ
ラックt?!!造するにあたり、前記熱分解部1および
熟成部2を下記の条件で操作することを特徴とするアセ
チレンブラックの製造方法。 熱分解部1:温度1900℃以上の分解生成物の雰囲気
に該分解生成物中 のカービンエアロゾルを標準 状態換算で30〜150秒滞 溜させる。 熟成部2:熱分解部から導入された温度1700℃以上
のカービンエア ロゾルを標準状態換算で20 〜90秒滞溜させる。
[Scope of Claims] Acetylene gas A or a raw material in which acetylene gas A contains unsaturated hydrocarbon B in an amount of 40 parts by weight or less of carbon in B based on 100 parts by weight of carbon in A is thermally decomposed. It consists of a section 1 and a ripening section 2, and the ratio (D + / D t) of the diameter D+ of the thermal decomposition section 1 to the diameter D2 of the ripening section 2 is 1.
.. 2 to 22, and the ratio LLs/Ltl of the length of the pyrolysis section 1 to the length of the aging section 2 is 0.4 to 1.0. Asena Reno Black T? ! ! A method for producing acetylene black, which comprises operating the thermal decomposition section 1 and the aging section 2 under the following conditions. Thermal decomposition part 1: The carbine aerosol in the decomposition product is allowed to remain in the atmosphere of the decomposition product at a temperature of 1900° C. or higher for 30 to 150 seconds in terms of standard conditions. Aging section 2: The carbine aerosol introduced from the thermal decomposition section and having a temperature of 1,700°C or higher is retained for 20 to 90 seconds in terms of standard conditions.
JP14999883A 1983-08-17 1983-08-17 Production of acetylene black Pending JPS6042465A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14999883A JPS6042465A (en) 1983-08-17 1983-08-17 Production of acetylene black

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14999883A JPS6042465A (en) 1983-08-17 1983-08-17 Production of acetylene black

Publications (1)

Publication Number Publication Date
JPS6042465A true JPS6042465A (en) 1985-03-06

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP14999883A Pending JPS6042465A (en) 1983-08-17 1983-08-17 Production of acetylene black

Country Status (1)

Country Link
JP (1) JPS6042465A (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5690860A (en) * 1979-12-24 1981-07-23 Denki Kagaku Kogyo Kk Carbon black manufacturing apparatus

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5690860A (en) * 1979-12-24 1981-07-23 Denki Kagaku Kogyo Kk Carbon black manufacturing apparatus

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