JPS5839577B2 - Cutlet Seitan No Saiseihou - Google Patents

Cutlet Seitan No Saiseihou

Info

Publication number
JPS5839577B2
JPS5839577B2 JP13402873A JP13402873A JPS5839577B2 JP S5839577 B2 JPS5839577 B2 JP S5839577B2 JP 13402873 A JP13402873 A JP 13402873A JP 13402873 A JP13402873 A JP 13402873A JP S5839577 B2 JPS5839577 B2 JP S5839577B2
Authority
JP
Japan
Prior art keywords
activated carbon
catalytic cracking
ozone
heating
regeneration
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
Application number
JP13402873A
Other languages
Japanese (ja)
Other versions
JPS5084493A (en
Inventor
勍己 岡山
信宏 八巻
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.)
Suido Kiko Kaisha Ltd
Original Assignee
Suido Kiko Kaisha Ltd
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 Suido Kiko Kaisha Ltd filed Critical Suido Kiko Kaisha Ltd
Priority to JP13402873A priority Critical patent/JPS5839577B2/en
Publication of JPS5084493A publication Critical patent/JPS5084493A/ja
Publication of JPS5839577B2 publication Critical patent/JPS5839577B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 オゾンは特有な酸化能力を有するので、脱臭、脱色等、
水処理等においても有効に利用されているが、オゾンの
水に対する溶解性が低いため、未反応ガスは大気中に放
散され、二次公害をおこすおそれがあるので、廃オゾン
ガスを活性炭等で接触分解したりして、その害を防止す
る必要がある。
[Detailed description of the invention] Ozone has a unique oxidizing ability, so it can be used for deodorization, decolorization, etc.
It is also effectively used in water treatment, etc., but due to the low solubility of ozone in water, unreacted gases may be released into the atmosphere and cause secondary pollution, so waste ozone gas is contacted with activated carbon, etc. It is necessary to prevent the damage by disassembling it.

しかし、接触分解操作に際し、高価な活性炭を使用する
ので、経済性から再生使用の可能性を検討すると、再生
方法としては、水洗法、薬品洗浄法、加熱法、水蒸気加
熱法などが一応考えられ、水洗による再生等も試みたが
、加熱法(空気加熱法)による場合が最も適当であると
考えられたので、ここにおいて、(1)低温度での再生
が可能か否か。
However, since expensive activated carbon is used in the catalytic cracking operation, when considering the possibility of recycling from an economic standpoint, the following recycling methods are considered: water washing, chemical washing, heating, steam heating, etc. Although attempts were made to regenerate the material by washing with water, it was thought that a heating method (air heating method) would be the most appropriate, so the following questions were asked: (1) Is it possible to regenerate at low temperatures?

(2)再生率はどの程度の条件で充分か。(2) What conditions are sufficient for the reproduction rate?

(3)その時の活性炭の消耗はどの程度か。(3) How much is the activated carbon consumed at that time?

(4)繰返し使用の可能性はどうか。(4) Is it possible to use it repeatedly?

等について実験を行った。従来水処理において、水中の
有機物質を接触分解した活性炭は、800℃〜1000
℃附近の高温で再生処理を行っているが、これは活性炭
の消耗を少くするために酸素の混入を少くすると、有機
汚染物質の一部が炭化されて活性炭上に残り、この炭化
物を高温度で賦活しなげれば、活性炭が再生されないと
考えているためである。
We conducted experiments on the following. In conventional water treatment, activated carbon, which has been used to catalytically decompose organic substances in water, is
The regeneration process is carried out at a high temperature around ℃, but this is because when the amount of oxygen mixed in is reduced to reduce consumption of the activated carbon, some of the organic pollutants are carbonized and remain on the activated carbon, and this charcoal is heated to a high temperature. This is because it is believed that if activated carbon is not activated, activated carbon will not be regenerated.

これに対し本発明における再生すべき活性炭は、その接
触分解されるガスはオゾンを含有した空気であり、水中
に含有する有機溶洗物質は存在しないことから、前記の
ような高温度での処理を行う必要はなく、ただオゾンと
活性炭の表面に生じた生成物だげを脱離すればよいわけ
である。
On the other hand, in the activated carbon to be regenerated in the present invention, the gas to be catalytically cracked is air containing ozone, and since there is no organic washing substance contained in water, the activated carbon cannot be treated at high temperatures as described above. There is no need to carry out this process; all that is needed is to remove the ozone and the product residue formed on the surface of the activated carbon.

オゾンと活性炭の接触反応に於て、C>C−0)の二重
結合部分の切断が行われるために活性炭にクラックを生
じ、高温の800℃前後の温度で加熱再生する場合は、
性能の回復は可能ではあるが、炭粒はぼろぼろになり、
原形を維持しえな(なる。
In the contact reaction between ozone and activated carbon, cracks occur in the activated carbon due to the cleavage of the C>C-0) double bond, and if the activated carbon is regenerated by heating at a high temperature of around 800°C,
Although it is possible to recover the performance, the charcoal grains will become tattered and
It cannot maintain its original form.

この現象をおさえるために、低温加熱を行い、再生能力
をチェックして、未使用炭と比較してみたところ、満足
すべき結果かえられ、場合によっては、未使用炭以上の
接触分解能力が上昇することも判明した。
In order to suppress this phenomenon, we performed low-temperature heating, checked the regeneration ability, and compared it with unused coal.We found satisfactory results, and in some cases, the catalytic cracking capacity increased even more than unused coal. It was also found that

次に実施例によりその状態を説明する。Next, the situation will be explained using an example.

例 先ず、水中を通じて出てきた湿潤オゾンガスを接触分解
して飽和に達した活性炭の一定体積30m1を採取して
、電気炉で加熱してから、加熱再生処理後の活性炭につ
いて同様にオゾン濃度4.5り7m3alr、カス風量
3J/分を流ジテオシン接触分解を行い、接触分解装置
の出口濃度を調べながら接触分解破過曲線をつくり比較
したところ、第1図に示すような結果が得られた。
First, a certain volume of 30 ml of activated carbon that has reached saturation by catalytically decomposing the moist ozone gas that has come out through water is collected and heated in an electric furnace. Catalytic cracking of ditheosin was carried out at a flow rate of 3 J/min at a flow rate of 3 J/min of waste, and the catalytic cracking breakthrough curves were created and compared while checking the outlet concentration of the catalytic cracking apparatus, and the results shown in Figure 1 were obtained.

即ち、実験の結果では、100℃の加熱温度では長時間
加熱しても、接触分解力は、はとんど回復せず、200
℃から接触分解力が回復してきた。
In other words, the experimental results show that even if heated for a long time at a heating temperature of 100°C, the catalytic cracking power hardly recovers and the
The catalytic cracking power has recovered from ℃.

そして、300℃では20分加熱で略々未使用炭の域ま
で接触分解能力が回復した。
At 300°C, the catalytic cracking ability was recovered to approximately the level of unused coal after 20 minutes of heating.

第1図をみると、この実験では300℃、20分処理の
活性炭が接触分解開始5時間前後では、未使用炭より優
れた性能を示している場合のあることもわかる。
Looking at FIG. 1, it can be seen that in this experiment, activated carbon treated at 300° C. for 20 minutes sometimes showed better performance than virgin carbon around 5 hours after the start of catalytic cracking.

そして再生繰返し使用による、接触分解力と摩滅率の変
化を調べるため、使用剤活性炭を最も条件のよい300
℃、20分電気炉で加熱再生し、同一条件でオゾンガス
の除去試験を行い、活性炭※※の劣化によりオゾンカス
の出口濃度が0.IVolp、p、mになった時のその
劣化に至る時間とその単位重量活性炭あたりのオゾンガ
ス接触分解状況を比較したのが第2図である。
In order to investigate the changes in catalytic cracking force and attrition rate due to repeated reuse, activated carbon was used under the best conditions.
℃ for 20 minutes in an electric furnace, and an ozone gas removal test was conducted under the same conditions. Due to the deterioration of the activated carbon, the ozone scum outlet concentration was 0. Figure 2 compares the time required for deterioration when IVolp, p, and m are reached and the state of ozone gas catalytic decomposition per unit weight of activated carbon.

又、摩滅率の変化については、試料の乾燥条件を一定に
して、上水道沢過砂試験法に準じて試験を行った結果、
下記表のような結果が得られた。
In addition, regarding the change in the wear rate, the drying conditions of the sample were kept constant and the test was conducted according to the waterworks stream sand test method.
The results shown in the table below were obtained.

この試験法は粒子を最初破砕機にかげてから篩分けする
もので、オゾンを接触分解すると粒子の強度は低下する
In this test method, the particles are first passed through a crusher and then sieved, and the strength of the particles decreases when the ozone is catalytically decomposed.

空気加熱再生による繰返し使用の際の変化は上記の通り
であるが活性炭の強度の劣化を考えるときはそのまま使
用のとき2回再生による3回使用位が限界のようである
The changes during repeated use due to air heating regeneration are as described above, but when considering the deterioration of the strength of activated carbon, it seems that when used as is, the limit is 3 uses due to 2 regenerations.

なお、オゾンを活性炭で処理する際の問題点としては爆
発現象があるが、低濃度の湿潤オゾンガスを接触させた
時は、爆発は見られなかったので、この点を装置設計に
当って考慮すべきである。
Although an issue with treating ozone with activated carbon is the explosion phenomenon, no explosion was observed when low-concentration wet ozone gas was brought into contact, so this point should be taken into account when designing the equipment. Should.

以上を総合すると、本発明方法は、 (1) 従来の再生温度800℃〜1000℃に比べ
200℃〜300℃と低温で再生できる。
To summarize the above, the method of the present invention: (1) Regeneration can be performed at a lower temperature of 200°C to 300°C compared to the conventional regeneration temperature of 800°C to 1000°C.

(2)低温で再生するので酸素含有ガスが混入しても活
性炭の消耗度が少ない。
(2) Since it is regenerated at low temperature, activated carbon is less consumed even if oxygen-containing gas is mixed in.

(3)部分的ではあるが、未使用炭より接触分解能力が
大きい場合も現われ、概して接触分解能力回復は良好で
ある。
(3) Although there are some cases where the catalytic cracking capacity is greater than that of unused coal, the recovery of the catalytic cracking capacity is generally good.

(4)300℃位で加熱するときは、処理は非常に短時
間でできる。
(4) When heating at around 300°C, the treatment can be done in a very short time.

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

添Vfff図面中、第1図は加熱再生による接触分解能
力の回復を示す図表であって、オゾン濃度4.5P/m
、活性炭量3Qmg、ガス風量31/分の条件でIは2
00℃1時間、■は200℃3時間、■は300℃10
分間、■は300℃20分間の夫々加熱再生を行ったも
の、■は未使用炭の接触分解破過曲線を夫々示す。 第2図は再生繰返しによる接触分解量の変化を示す図表
であって、300℃20分間の加熱再生を行ったものに
ついてオゾン濃度2 ′iI/ m’、活性炭量105
m11ガス風量7. Ol:7分の条件で、300℃2
0分間の加熱再生を行ったもので、0は未使用炭、1は
1回再生炭、2は2回再生炭、3は3回再生炭の接触分
解能力の曲線である。
In the attached Vfff drawing, Figure 1 is a chart showing the recovery of catalytic cracking capacity by heating regeneration, and the ozone concentration is 4.5P/m.
, I is 2 under the conditions of activated carbon amount 3Qmg and gas flow rate 31/min.
00℃ 1 hour, ■ 200℃ 3 hours, ■ 300℃ 10
(2) shows the catalytic cracking breakthrough curve of unused coal. Figure 2 is a chart showing changes in the amount of catalytic decomposition due to repeated regeneration, and shows the ozone concentration of 2'iI/m' and the amount of activated carbon of 105 after heat regeneration at 300°C for 20 minutes.
m11 gas air volume 7. Ol: 300℃2 for 7 minutes
The graph shows the catalytic cracking ability curves after 0 minutes of heating regeneration, where 0 is unused coal, 1 is once regenerated coal, 2 is twice regenerated coal, and 3 is three times regenerated coal.

Claims (1)

【特許請求の範囲】[Claims] 1 活性炭の加熱再生処理法において、湿潤したオゾン
ガスを接触反応する機能の衰退により未分解オゾンガス
が検知される如くなった活性炭を、200℃〜300℃
の温度で10分間〜1時間の加熱処理を行うことを特徴
とする、活性炭の再生法。
1 In the thermal regeneration treatment method for activated carbon, activated carbon whose ability to catalytically react wet ozone gas has deteriorated and undecomposed ozone gas can be detected is heated to 200°C to 300°C.
A method for regenerating activated carbon, the method comprising performing heat treatment at a temperature of 10 minutes to 1 hour.
JP13402873A 1973-12-01 1973-12-01 Cutlet Seitan No Saiseihou Expired JPS5839577B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13402873A JPS5839577B2 (en) 1973-12-01 1973-12-01 Cutlet Seitan No Saiseihou

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13402873A JPS5839577B2 (en) 1973-12-01 1973-12-01 Cutlet Seitan No Saiseihou

Publications (2)

Publication Number Publication Date
JPS5084493A JPS5084493A (en) 1975-07-08
JPS5839577B2 true JPS5839577B2 (en) 1983-08-31

Family

ID=15118678

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13402873A Expired JPS5839577B2 (en) 1973-12-01 1973-12-01 Cutlet Seitan No Saiseihou

Country Status (1)

Country Link
JP (1) JPS5839577B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63101763A (en) * 1986-10-17 1988-05-06 Tokin Corp Current detector
JPH01124568U (en) * 1988-02-16 1989-08-24
JPH02259471A (en) * 1989-03-30 1990-10-22 Tokin Corp Current detector

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63101763A (en) * 1986-10-17 1988-05-06 Tokin Corp Current detector
JPH01124568U (en) * 1988-02-16 1989-08-24
JPH02259471A (en) * 1989-03-30 1990-10-22 Tokin Corp Current detector

Also Published As

Publication number Publication date
JPS5084493A (en) 1975-07-08

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