JPS61178027A - Treatment of exhaust gas containing halogenated hydrocarbon - Google Patents
Treatment of exhaust gas containing halogenated hydrocarbonInfo
- Publication number
- JPS61178027A JPS61178027A JP60019119A JP1911985A JPS61178027A JP S61178027 A JPS61178027 A JP S61178027A JP 60019119 A JP60019119 A JP 60019119A JP 1911985 A JP1911985 A JP 1911985A JP S61178027 A JPS61178027 A JP S61178027A
- Authority
- JP
- Japan
- Prior art keywords
- exhaust gas
- halogenated hydrocarbon
- carbon
- passed
- gas containing
- 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
Landscapes
- Treating Waste Gases (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、有毒な気相のノ10ゲン化炭化水素を含むガ
スを処理する方法に関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a method for treating gases containing toxic gas-phase 10-genated hydrocarbons.
(従来技術とその問題点)
近年、高温での気相反応例えば揮発性の金属ハロゲン化
物、金属の有機化合物、炭化水素化合物等の熱分解、水
素還元及び置換反応によって、黒鉛、金属等の基材表面
に炭素、炭化物、珪化物等を蒸着する化学蒸着法が盛ん
に用いられている。(Prior art and its problems) In recent years, groups such as graphite and metals have been produced by gas phase reactions at high temperatures, such as thermal decomposition of volatile metal halides, metal organic compounds, hydrocarbon compounds, hydrogen reduction, and substitution reactions. Chemical vapor deposition methods are widely used to deposit carbon, carbide, silicide, etc. on the surface of materials.
この中でハロゲン化炭化水素は、熱分解炭素の生成、炭
化珪素を析出させる為の炭素源等として幅広く用いられ
ている。Among these, halogenated hydrocarbons are widely used as a carbon source for generating pyrolytic carbon and depositing silicon carbide.
ハロゲン化炭化水素は有毒であシ、又S i C1a等
の金属ハロゲン化物と異なり常温では空気中及び水中で
安定なものが多い。例えばジクロロエタン。Halogenated hydrocarbons are toxic, and unlike metal halides such as S i C1a, many of them are stable in air and water at room temperature. For example dichloroethane.
ジクロロエチレン、トリクロロエタン、t’)/ロロエ
チレン、テトラクロロエチレン又はそれらの誘導体がそ
うである。Examples include dichloroethylene, trichloroethane, t')/loloethylene, tetrachloroethylene, or derivatives thereof.
しかし、ハロゲン化炭化水素を用いて気相反応を行なっ
た後の排ガス中には未反応のハロゲン化炭化水素が含ま
れているにもかかわらず、その効果的な処理が殆んど行
なわれていないのが現状である。例えば反応室を減圧に
保つ為のロータリーポンプ等の真空排気装置から排出さ
れる排ガスを水やアルカリ溶液で処理する方法が知られ
ているが、この方法は塩化水素ガスには有効でも)sロ
ゲン化炭化水素には効果がない。しかも有機塩化物の排
出規制はp、 p、 b、オーダーに及ぶ厳し、いもの
であることを考えると、これらハロゲン化炭化水素は完
全く分解又は分離保存することが望まれる。However, although unreacted halogenated hydrocarbons are contained in the exhaust gas after a gas-phase reaction using halogenated hydrocarbons, there are few effective ways to treat them. The current situation is that there is no such thing. For example, a method is known in which the exhaust gas discharged from a vacuum evacuation device such as a rotary pump to maintain a reduced pressure in the reaction chamber is treated with water or an alkaline solution, but this method is effective against hydrogen chloride gas (s). Hydrocarbons have no effect. Moreover, considering that the emission regulations for organic chlorides are strict, ranging from P, P, B, orders of magnitude, it is desirable that these halogenated hydrocarbons be completely decomposed or separated and stored.
一方ハロゲン化炭化水素によって真空排気装置が劣化す
るという問題もある。On the other hand, there is also the problem that halogenated hydrocarbons deteriorate the vacuum evacuation equipment.
(発明の目的)
本発明は、上記した問題を解消するハロゲン化炭化水素
含有排ガスを処理する方法に関する。(Object of the invention) The present invention relates to a method for treating halogenated hydrocarbon-containing exhaust gas that eliminates the above-mentioned problems.
(問題点を解決するための手段)
本発明は、ハロゲン化炭化水素を含有する排ガスを空気
と混合した後、600℃以上に加熱した熱処理管の中を
3秒以上通し1次いで固形アルカリ充填槽を通過させる
ハロゲン化炭化水素含有排ガスを処理する方法に関する
。(Means for Solving the Problems) The present invention involves mixing exhaust gas containing halogenated hydrocarbons with air, passing it through a heat treatment tube heated to 600°C or higher for 3 seconds or more, and then passing it through a solid alkali filling tank. The present invention relates to a method for treating halogenated hydrocarbon-containing exhaust gas that is passed through.
本発明で、上記加熱温度は900℃以上にすればハロゲ
ン化炭化水素の分解が促進されて好ましい。熱処理管の
材質9寸法・形状について特に制限はないが、蛇管又は
螺旋管等を用いれば小さいスペースでガスが通過する熱
処理部を長くでき排ガスを充分に分解できるので好まし
い。前記熱処理においてハロゲン化炭化水素は炭素及び
ハロゲン化水素に分解されるが、この炭素を熱処理管内
で酸化させてガス化して排出させるために、排ガスを熱
処理管に送る前に空気と混合させる。混合は、排ガスを
例えば混合室に送り、混合室に設けた空気導入口から埋
置調節弁を用いて適量の空気を導入し混合する。混合は
排ガスと空気が均一に混合できればよく、方法、構造等
に制限はない。In the present invention, it is preferable to set the heating temperature to 900° C. or higher because decomposition of the halogenated hydrocarbon is promoted. There are no particular restrictions on the size and shape of the material 9 of the heat treatment tube, but it is preferable to use a serpentine tube or a spiral tube because the heat treatment section through which the gas passes can be lengthened in a small space and the exhaust gas can be sufficiently decomposed. In the heat treatment, the halogenated hydrocarbon is decomposed into carbon and hydrogen halide. In order to oxidize the carbon in the heat treatment tube, gasify it, and discharge it, the exhaust gas is mixed with air before being sent to the heat treatment tube. For mixing, exhaust gas is sent to, for example, a mixing chamber, and an appropriate amount of air is introduced and mixed through an air inlet provided in the mixing chamber using a buried control valve. There are no restrictions on the mixing method, structure, etc., as long as the exhaust gas and air can be mixed uniformly.
均一混合の為には混合行程をある程度長くしたり攪拌す
ることが好ましい。空気量は炭素との反応に必要な量よ
り過剰に加える。For uniform mixing, it is preferable to extend the mixing process to some extent or to stir. The amount of air added is in excess of the amount required for reaction with carbon.
本発明において、熱処理管の加熱温度が600℃未満及
び排ガスを通す時間が3秒未満であるとハロゲン化炭化
水素は分解されるが1分解して生成した炭素微粉を酸化
させるには不充分である。In the present invention, if the heating temperature of the heat treatment tube is less than 600°C and the time for passing the exhaust gas is less than 3 seconds, the halogenated hydrocarbon will be decomposed, but it will not be enough to oxidize the carbon fine powder produced by decomposition. be.
熱処理管からの排ガスは固形アルカリ充填槽全通して含
有するハロゲン化水素を除去する。アルカリ充填槽の帯
造、01!用するアルカリの穐類等はハロゲン化水素が
充分除去できるものであればよく特に制限はない。The exhaust gas from the heat treatment tube passes through the solid alkali-filled tank to remove the hydrogen halide contained therein. Obi-zukuri of alkaline filling tank, 01! There are no particular limitations on the alkali used, as long as it can sufficiently remove hydrogen halides.
本発明の方法は化学蒸着法と併用して用いることが好ま
しい。化学蒸着における気相反応は減圧しながら原料ガ
スをキャリアーガスと共に送って行なうのが一般である
から、化学蒸着装置の反応室と減圧装置との間に空気混
合室、熱処理管及び固形アルカリ充填槽を付加すればよ
い。併用しない場合は送(排)気ポンプ、アスピレータ
−等全付加してガスの流れをよくすることが好ましい。Preferably, the method of the present invention is used in combination with a chemical vapor deposition method. Gas-phase reactions in chemical vapor deposition are generally carried out by sending the raw material gas together with a carrier gas while reducing the pressure. Just add. If not used together, it is preferable to add an air supply (exhaust) pump, an aspirator, etc. to improve the gas flow.
(実施例)
第1図は化学蒸着法と本発明の方法とを併用した場合の
工程図を示す。真空ポンプ8を稼動させ。(Example) FIG. 1 shows a process diagram when the chemical vapor deposition method and the method of the present invention are used together. Operate vacuum pump 8.
減圧調節弁7を開いて反応室10を減圧してから。After opening the pressure reduction control valve 7 and reducing the pressure in the reaction chamber 10.
流を調節弁1を開いてハロゲン化炭化水素を含むガスと
キャリアーガスとの混合ガスAt−反応室10に導く。The flow is introduced into the At-reaction chamber 10 by opening the control valve 1 and introducing a mixture of gas containing halogenated hydrocarbon and carrier gas.
基材2は高周波誘導コイル3によって直接的に加熱され
、4人された混合ガス中のハロゲン化炭化水素を含むガ
スは前記加熱された基材に接触して反応し、基材2の上
に析出物Bi付着させる。以後流量調節弁1及び減圧調
節弁7tl−適宜操作して反応室10を減圧に保ち上記
反応を継続させる。反応室10を通過した排ガスは混合
室11に導かれ、空気導入口13から流量調節弁12を
通って流入してくる空気Cと混合され、電気炉5で加熱
された管内径10mm、巻数20回の螺旋管4を通る過
程で炭素とハロゲン化水素に分解され、炭素は螺旋管中
で直ちに空気中の酸素によって炭酸ガスとなる。螺旋管
を抜けた排ガスは固形アルカリ充填槽15を通ってハロ
ゲン化炭化水素が除去され、真空ポンプ8により排ガス
Gとして排出される。9はガス検知器、14は逆流防止
弁である。The base material 2 is directly heated by the high frequency induction coil 3, and the gas containing the halogenated hydrocarbon in the mixed gas contacts the heated base material and reacts, and is heated on the base material 2. A precipitate of Bi is deposited. Thereafter, the flow rate control valve 1 and the pressure reduction control valve 7tl are appropriately operated to maintain the reaction chamber 10 at a reduced pressure to continue the above reaction. The exhaust gas that has passed through the reaction chamber 10 is led to a mixing chamber 11, where it is mixed with air C that flows in from an air inlet 13 through a flow rate control valve 12, and is heated in an electric furnace 5 using a tube with an inner diameter of 10 mm and a number of turns of 20. During the process of passing through the spiral tube 4, the carbon is decomposed into carbon and hydrogen halide, and the carbon is immediately converted into carbon dioxide by oxygen in the air in the spiral tube. The exhaust gas that has passed through the spiral tube passes through a solid alkali filling tank 15 to remove halogenated hydrocarbons, and is discharged as exhaust gas G by a vacuum pump 8. 9 is a gas detector, and 14 is a check valve.
上記方法において、混合ガスAに1,111−ト!Jク
ロロエタン(和光純系製試薬1級)20容量チ及びキャ
リアーガスとしてアルゴン80容量チ。In the above method, 1,111-t! 20 volumes of J chloroethane (grade 1 reagent manufactured by Wako Pure Chemical Industries, Ltd.) and 80 volumes of argon as a carrier gas.
基材2にピッチコークス系人造黒鉛を用い9反応室10
内の圧力を40mmHg、混合ガスAの流量を毎分20
0mt!、基材2の温度を800℃として反応を行なわ
せ、熱分解炭素を基材2の上に析出させた。排ガスに混
合する導入空気Cの流量を毎分600m1!、排ガスを
分解させる螺旋管4の温度を1000℃として螺旋管4
を3秒で通過させた。9 reaction chambers 10 using pitch coke-based artificial graphite as the base material 2
The pressure inside is 40mmHg, and the flow rate of mixed gas A is 20mmHg/min.
0mt! The temperature of the substrate 2 was set to 800° C. to carry out the reaction, and pyrolytic carbon was deposited on the substrate 2. The flow rate of introduced air C mixed with exhaust gas is 600 m1 per minute! , the temperature of the spiral tube 4 that decomposes the exhaust gas is set to 1000°C.
passed in 3 seconds.
螺旋管4を通過したガスを、径5mmの粒状苛性ソーダ
(和光紬薬製試薬特級)2009が充填された固形アル
カリ充填槽15を通過させて塩化水素(HCIりを吸収
させ、検出器9(日立ガスクロマトグラフ023型)で
分析した結果未反応ハロゲン化炭化水素は全く見られず
、 HC1!は僅かにo、oos容童チを示すだけでめ
った。The gas that has passed through the spiral tube 4 is passed through a solid alkali-filled tank 15 filled with granular caustic soda (special grade reagent manufactured by Wako Tsumugi Co., Ltd.) 2009 with a diameter of 5 mm to absorb hydrogen chloride (HCI). As a result of analysis using a gas chromatograph (Model 023), no unreacted halogenated hydrocarbons were found, and HC1! showed only slight o, oos and oxidation.
(発明の効果)
本発明によれば、ハロゲン化炭化水素は完全に分解され
9分解生成物も無害なものだけ排出することが可能とな
り、真空排気装置の劣化も防止出来る。(Effects of the Invention) According to the present invention, halogenated hydrocarbons are completely decomposed and only harmless decomposition products can be discharged, and deterioration of the vacuum evacuation device can also be prevented.
第1図は本発明の実施例における排ガス処理を示す工程
図である。
符号の説明
1・・・流量調節弁 2・・・基材3・・・^周
波誘導コイル 4・・・螺旋管5・・・電気炉
7・・・減圧調節弁8・・・真空ポンプ 9
・・・ガス検知器10・・・反応室 11・
・・混合室12・・・流量調節弁 13・・・空気
導入口14・・・逆流防止弁
15・・・固形アルカリ充填槽
知・−・FIG. 1 is a process diagram showing exhaust gas treatment in an embodiment of the present invention. Explanation of symbols 1...Flow control valve 2...Base material 3...^Frequency induction coil 4...Spiral tube 5...Electric furnace
7... Pressure reduction control valve 8... Vacuum pump 9
...Gas detector 10...Reaction chamber 11.
...Mixing chamber 12...Flow rate control valve 13...Air inlet 14...Backflow prevention valve 15...Solid alkali filling tank control...
Claims (1)
した後、600℃以上に加熱した熱処理管の中を3秒以
上通し、次いで固形アルカリ充填槽を通過させることを
特徴とするハロゲン化炭化水素含有排ガスを処理する方
法。1. Halogenated hydrocarbon, which is characterized by mixing the exhaust gas containing the halogenated hydrocarbon with air, passing it through a heat treatment tube heated to 600°C or more for 3 seconds or more, and then passing it through a solid alkali-filled tank. A method of treating contained exhaust gas.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60019119A JPS61178027A (en) | 1985-02-01 | 1985-02-01 | Treatment of exhaust gas containing halogenated hydrocarbon |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60019119A JPS61178027A (en) | 1985-02-01 | 1985-02-01 | Treatment of exhaust gas containing halogenated hydrocarbon |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS61178027A true JPS61178027A (en) | 1986-08-09 |
Family
ID=11990579
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60019119A Pending JPS61178027A (en) | 1985-02-01 | 1985-02-01 | Treatment of exhaust gas containing halogenated hydrocarbon |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61178027A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0463133A (en) * | 1990-06-11 | 1992-02-28 | Agency Of Ind Science & Technol | Decomposition device for organic halogen compound |
JPH0463132A (en) * | 1990-06-11 | 1992-02-28 | Agency Of Ind Science & Technol | Decomposition device for organic halogen compound |
JPH0463131A (en) * | 1990-06-11 | 1992-02-28 | Agency Of Ind Science & Technol | Decomposition device for organic halogen compound |
US10981107B2 (en) * | 2015-03-27 | 2021-04-20 | The Boeing Company | Centrifugal air separators |
US11235279B2 (en) | 2016-02-23 | 2022-02-01 | The Boeing Company | Centrifugal air separator coil manufacturing methods |
-
1985
- 1985-02-01 JP JP60019119A patent/JPS61178027A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0463133A (en) * | 1990-06-11 | 1992-02-28 | Agency Of Ind Science & Technol | Decomposition device for organic halogen compound |
JPH0463132A (en) * | 1990-06-11 | 1992-02-28 | Agency Of Ind Science & Technol | Decomposition device for organic halogen compound |
JPH0463131A (en) * | 1990-06-11 | 1992-02-28 | Agency Of Ind Science & Technol | Decomposition device for organic halogen compound |
US10981107B2 (en) * | 2015-03-27 | 2021-04-20 | The Boeing Company | Centrifugal air separators |
US11235279B2 (en) | 2016-02-23 | 2022-02-01 | The Boeing Company | Centrifugal air separator coil manufacturing methods |
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