JPS6037048B2 - Activated carbon manufacturing method - Google Patents
Activated carbon manufacturing methodInfo
- Publication number
- JPS6037048B2 JPS6037048B2 JP55136019A JP13601980A JPS6037048B2 JP S6037048 B2 JPS6037048 B2 JP S6037048B2 JP 55136019 A JP55136019 A JP 55136019A JP 13601980 A JP13601980 A JP 13601980A JP S6037048 B2 JPS6037048 B2 JP S6037048B2
- Authority
- JP
- Japan
- Prior art keywords
- activated carbon
- adsorption
- activation
- producing activated
- grains
- 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
Landscapes
- Carbon And Carbon Compounds (AREA)
Description
【発明の詳細な説明】
本発明は現在過剰が問題となっている古米等の穀類を原
料としたミクロポア−の粉末活性炭の製造方法に関し、
特に賦活工程を二段階にした活性炭の製造方法に関する
。[Detailed Description of the Invention] The present invention relates to a method for producing micropore powdered activated carbon made from grains such as old rice, which is currently a problem in excess.
In particular, the present invention relates to a method for producing activated carbon in which the activation process is performed in two stages.
一般に粉末活性炭の製造方法として、原料にオガ肩、木
炭等を主として用いた水蒸気賦活法或は塩化亜鉛賦活法
等が知られている。Generally, methods for producing powdered activated carbon include a steam activation method, a zinc chloride activation method, etc., which mainly use sawdust, charcoal, etc. as raw materials.
水蒸気賦活法は400〜500qoで炭化したオガ屑又
は8〜30メッシュに破砕整粒した木炭を700〜90
0qoで水蒸気を添加して賦活艮0ち活性化せしめる方
法であり、また塩化亜鉛賦活法はオガ屑等を乾燥した後
、塩化亜塩と塩酸の混合液に侵債熟成させて500〜6
00ooで鱈焼する方法である。これら一般的な製造法
により製造された粉末活性炭は、吸着紬孔が大きい所謂
マクロポァーに属し、液相中で脱色や吸着反応を行う液
相吸着に用いるには適しているが、自動車の蒸発燃料の
吸着或は農園芸用として土壌中に発生する不純バクテリ
アの吸着に使用する活性炭としては適していない。The steam activation method uses sawdust carbonized at 400 to 500 qo or charcoal crushed to 8 to 30 mesh and 700 to 90 qo
This is a method of activating by adding water vapor at 0qo, and the zinc chloride activation method involves drying sawdust, etc., and then ripening it in a mixed solution of subsalt chloride and hydrochloric acid.
This is a method of grilling cod at 00oo. Powdered activated carbon manufactured by these general manufacturing methods belongs to the so-called macropore type with large adsorption pores, and is suitable for use in liquid phase adsorption that performs decolorization and adsorption reactions in the liquid phase. It is not suitable as activated carbon for adsorption of impure bacteria generated in soil for agricultural and horticultural purposes.
即ち、蒸発燃料の吸着等は気相吸着であるため、吸着紬
孔の小さいミクロポアーの活性炭が必要とされ、斯るミ
クロポアーの活性炭の製造方法が望まれている。本発明
者は上述の如き問題的に鑑み本発明を成したものであり
、その目的とする処は蒸発燃料の吸着等の気相吸着に適
した活性炭の製造方法を提供するにあり、斯る目的を達
成すべく本発明は米穀等の穀類にケイ酸ナトリウム又は
樟藻±類のうち少くとも一方を添加して乾留し、これを
所定の条件下で炭化し、次いでこの炭化物に水蒸気を添
加し、更に炭酸ガスを添加して賦活することを特徴とし
ている。That is, since vapor phase adsorption is used to adsorb evaporated fuel, micropore activated carbon with small adsorption pores is required, and a method for producing such micropore activated carbon is desired. The present inventor has devised the present invention in view of the above-mentioned problems, and the purpose thereof is to provide a method for producing activated carbon suitable for vapor phase adsorption such as adsorption of evaporated fuel. In order to achieve the object, the present invention involves adding at least one of sodium silicate or camphor algae to grains such as rice, carbonizing it under predetermined conditions, and then adding steam to this carbonized product. It is characterized in that it is further activated by adding carbon dioxide gas.
以下に古玄米を原料とした場合の製造法につき説明する
。The manufacturing method using old brown rice as the raw material will be explained below.
原料として使用する古玄米は通常長径が7〜8側の楕円
粒状物であり、成分は炭水化物を王とし他に油脂質物、
糖、アミノ酸類等及び水分約15%を含有している。The old brown rice used as a raw material is usually oval granules with a major axis of 7 to 8 sides, and the main components are carbohydrates, oils and lipids, etc.
Contains sugar, amino acids, etc. and approximately 15% water.
上記の古玄米を乾燥して含有水分を上記の1/3以下と
し、炭化活性処理を容易にするため破砕整粒して直径0
.2〜0.7肋の頚粒状とする。次いで得られた顎粒物
にケイ酸ナトリウム又は桂藻土類を添加してロータリー
キルンに投入し、温度300〜350二0で乾留して原
料中の油脂質物、糖、アミノ酸類を除去する。The above old brown rice is dried to reduce the water content to 1/3 or less of the above amount, and then crushed and sized to make the carbonization process easier.
.. Shape into neck grains with 2 to 0.7 ribs. Next, sodium silicate or cinnamon earth is added to the obtained jaw granules, and the mixture is put into a rotary kiln and carbonized at a temperature of 300 to 35,020 ℃ to remove oil lipids, sugars, and amino acids in the raw materials.
乾留工程の次に炭化工程に入るわけであるが、炭化工程
における条件が吸着紬孔の構造を決定するため、活性炭
製造工程中最も重要である。The carbonization step follows the carbonization step, and since the conditions in the carbonization step determine the structure of the adsorption pores, it is the most important step in the activated carbon production process.
即ち、気相吸着に適するミクロポアーの活性炭を得るに
は温度等の炭化条件を適切に制御すること、更に炭化物
中の揮発成分の残存量が適当でなければならない。炭化
物中の揮発物が多い場合には、賦活加熱中に相乗発熱現
象により賦宿時間が短縮され賦活中に発達する吸着構造
がマイクロポアーとなる。したがって本発明における炭
化工程は、温度を500oo以下に押え、炉内滞留時間
を60〜90分にすると共に塩化カルシウムを添加して
緩慢な炭化を行なわしめる。このようにして得られた炭
化物の揮発分は約15%、固定炭素は約62%であり、
従来のオガ肩の炭化物或は雑木よりつくった木炭の揮発
分が約30%、固定炭素が約60%であるのに比べ、揮
発分が約半分に減少している。次に上記炭化工程により
得られた炭化物を賦活工程によって活性化せしめる。That is, in order to obtain micropore activated carbon suitable for gas phase adsorption, carbonization conditions such as temperature must be appropriately controlled, and the amount of volatile components remaining in the carbide must be appropriate. When there are many volatile substances in the carbide, the activation time is shortened due to a synergistic exothermic phenomenon during activation heating, and the adsorption structure that develops during activation becomes micropores. Therefore, in the carbonization step of the present invention, the temperature is kept below 500 oo, the residence time in the furnace is set to 60 to 90 minutes, and calcium chloride is added to effect slow carbonization. The volatile content of the carbide thus obtained was approximately 15%, and the fixed carbon content was approximately 62%.
Compared to conventional charcoal made from sawdust carbide or miscellaneous wood, which has a volatile content of about 30% and a fixed carbon content of about 60%, the volatile content has been reduced to about half. Next, the carbide obtained by the carbonization step is activated by an activation step.
本実施例においては賦活工程を賦宿ゾーンとエッチング
ゾーンの一段階に分けて賦活を行っている。即ち、ロー
タリーキルンの前半部を水蒸気を瞬間的に添加する賦活
ゾーンとし、後半部を炭酸ガスを供給して賦活反応助成
を行なうエッチングゾーンとしている。In this embodiment, the activation process is divided into one stage, an activation zone and an etching zone. That is, the first half of the rotary kiln is used as an activation zone where steam is added instantaneously, and the second half is used as an etching zone where carbon dioxide gas is supplied to assist the activation reaction.
表1は賦活時間、温度、水蒸気の添加量等を変化せしめ
て得られる活性炭の吸着性能への影響の実験結果を表わ
すものである。表1米穀を原料にした粉末活性炭製造の
賦活条件表1から明らかな如く賦宿時間は90〜180
分であることが好ましく、且つ賭活温度は1000〜1
100℃が最適であり、11500のこなると吸着性能
は低下し、また添加する水蒸気量も炭化物の1.M音以
上が好ましいことが分かる。Table 1 shows the experimental results of the effects on the adsorption performance of activated carbon obtained by varying the activation time, temperature, amount of water vapor added, etc. Table 1 Activation conditions for producing powdered activated carbon using rice as raw material As is clear from Table 1, the activation time is 90 to 180
It is preferable that the heating temperature is 1000 to 1 minute.
The optimal temperature is 100°C, and adsorption performance decreases when the temperature exceeds 11,500°C, and the amount of water vapor added is also 1.5°C. It can be seen that M sound or higher is preferable.
以上説明した工程により得られた活性炭はミクロポアー
の吸着細孔を有し、吸着持続性に富んだものである。The activated carbon obtained by the above-described process has micropores for adsorption and is highly durable in adsorption.
以下にその吸着能を表2及び添付図面を参照しつつ従来
のオガ肩又は木炭を原料とした活性炭との比較において
説明する。表2は本発明方法による活性炭と従来方法に
よる活性炭のカラメルの脱色率とメチレンフルー色素の
吸着率を比較したものである。The adsorption capacity will be explained below in comparison with conventional sawdust or activated carbon made from charcoal, with reference to Table 2 and the attached drawings. Table 2 compares the caramel decolorization rate and methylene flu dye adsorption rate of activated carbon according to the method of the present invention and activated carbon according to the conventional method.
表 2
種類別活性炭の液相吸着比
カラメル脱色試験はJIS規格に定められたカラメル液
を用い、各種活性炭に3び分間吸着反応なさしめた後の
脱色率を光電光度計を用いて計測したものであり、メチ
レンフルーの吸着試験は各種活性炭の吸着量をケミカル
バランスを用いて計測したものである。Table 2 Liquid phase adsorption ratio of activated carbon by type The caramel decolorization test uses caramel liquid specified in JIS standards, and the decolorization rate is measured using a photometer after adsorption reaction is performed on various activated carbons for 3 minutes. The adsorption test for methylene flue was carried out by measuring the adsorption amount of various activated carbons using chemical balance.
表の数値より明らかな如く本発明方法による活性炭はマ
クロポア−活性炭により吸着されるカラメル色素の吸着
度は低く、ミクロポアー活性炭により吸着されるメチレ
ンブルーの如き塩基性色素の吸着性が高いということか
ら吸着紬孔がミクロポアーに構成されていることが分か
る。As is clear from the values in the table, the activated carbon produced by the method of the present invention has a low degree of adsorption of caramel dyes adsorbed by the macropore activated carbon, and a high degree of adsorption of basic dyes such as methylene blue, which is adsorbed by the micropore activated carbon. It can be seen that the pores are structured into micropores.
また図は吸着持続性を比較したグラフであり、メチレン
フルーの2%水溶液に各種活性炭を入れ、吸着性を光電
光度計を用いて単位時間毎に測定したものである。The figure is a graph comparing adsorption persistence, in which various activated carbons were added to a 2% aqueous solution of methylene flue, and the adsorption properties were measured every unit time using a photometer.
このグラフより本発明方法による活性炭が吸着持続性に
優れていることが分かる。以上述べた如く本発明によれ
ば、古玄米等の穀類をケイ酸ナトリウム又は桂藻士類と
共に乾留して油脂質物、糖、アミノ酸類を除去した後、
適切なる条件下において緩慢に焼成炭化せしめ、微細孔
化された炭化物を得、これに所定温度下において水蒸気
を添化し更に炭酸ガスを添加する二段階の賦活工程にお
いて活性化せしめたので、余剰米を有効に利用でき省資
源に役立つとともに、気相吸着に好適なミクロポア−な
吸着紬孔を有し、吸着性能を持続性に富む活性炭を得る
ことができる。This graph shows that the activated carbon produced by the method of the present invention has excellent adsorption durability. As described above, according to the present invention, after carbonizing grains such as old brown rice with sodium silicate or cinnamon to remove oil lipids, sugars, and amino acids,
Slow calcination carbonization under appropriate conditions yields microporous carbide, which is then activated in a two-step activation process in which water vapor is added to this at a predetermined temperature and carbon dioxide gas is further added. It is possible to obtain activated carbon that can be used effectively and help conserve resources, has micropores suitable for gas phase adsorption, and has long-lasting adsorption performance.
図面は本発明方法による活性炭と従来法による活性炭の
吸着持続性を比較したグラフである。The drawing is a graph comparing the adsorption sustainability of activated carbon according to the method of the present invention and activated carbon according to the conventional method.
Claims (1)
とも一方を添加して乾留する工程と、この乾流した穀類
を炭化する工程と、この炭化物に水蒸気を添加する工程
と炭酸ガスを添加する工程とからなる二段階の賦活工程
とからなる活性炭の製造方法。 2 前記穀類は米穀であることを特徴とする特許請求の
範囲第1項記載の活性炭の製造方法。 3 前記穀類は乾燥され且つ破砕整粒されたものである
ことを特徴とする特許請求の範囲第1項又は第2項記載
の活性炭の製造方法。 4 前記炭化工程は塩化カルシウムを添加して行なうこ
とを特徴とする特許請求の範囲第1項から第3項のいず
れかに記載の活性炭の製造方法。 5 前記炭化工程の温度は500℃以下で且つ炭化工程
の時間は60分乃至90分であることを特徴とする特許
請求の範囲第1項から第4項のいずれかに記載の活性炭
の製造方法。 6 前記賦活工程の温度は1000℃乃至1100℃の
範囲で且つ賦活工程の時間は90分乃至180分である
ことを特徴とする特許請求の範囲第1項から第5項のい
ずれかに記載の活性炭の製造方法。[Claims] 1. A step of adding at least one of sodium silicate or diatomaceous earth to grains and carbonizing the grains, carbonizing the dry-flowed grains, and adding steam to the carbonized product. A method for producing activated carbon, which comprises a two-step activation process consisting of a process of adding carbon dioxide gas. 2. The method for producing activated carbon according to claim 1, wherein the grain is rice grain. 3. The method for producing activated carbon according to claim 1 or 2, wherein the grains are dried, crushed and sized. 4. The method for producing activated carbon according to any one of claims 1 to 3, wherein the carbonization step is performed by adding calcium chloride. 5. The method for producing activated carbon according to any one of claims 1 to 4, wherein the temperature of the carbonization step is 500° C. or less, and the time of the carbonization step is 60 minutes to 90 minutes. . 6. The method according to any one of claims 1 to 5, characterized in that the temperature of the activation step is in the range of 1000° C. to 1100° C., and the time of the activation step is 90 minutes to 180 minutes. Method for producing activated carbon.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP55136019A JPS6037048B2 (en) | 1980-09-30 | 1980-09-30 | Activated carbon manufacturing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP55136019A JPS6037048B2 (en) | 1980-09-30 | 1980-09-30 | Activated carbon manufacturing method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5761610A JPS5761610A (en) | 1982-04-14 |
JPS6037048B2 true JPS6037048B2 (en) | 1985-08-23 |
Family
ID=15165278
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP55136019A Expired JPS6037048B2 (en) | 1980-09-30 | 1980-09-30 | Activated carbon manufacturing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6037048B2 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006096568A (en) * | 2004-09-28 | 2006-04-13 | Shiga Pref Gov | Method for producing activated carbon |
DE102007050971B4 (en) * | 2007-03-14 | 2014-12-31 | BLüCHER GMBH | Process for the preparation of high performance adsorbents based on activated carbon with high meso- and macroporosity, high performance adsorbents and their use |
US8198210B2 (en) * | 2010-05-27 | 2012-06-12 | Corning Incorporated | Halogenated activated carbon materials for high energy density ultracapacitors |
KR102506938B1 (en) * | 2018-02-02 | 2023-03-07 | 현대자동차 주식회사 | Method for manufacturing activated carbon |
CN108773841B (en) * | 2018-06-26 | 2020-11-13 | 广西师范大学 | Porous carbon material prepared from waste diatomite and preparation method and application thereof |
-
1980
- 1980-09-30 JP JP55136019A patent/JPS6037048B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS5761610A (en) | 1982-04-14 |
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