JP2013184132A5 - - Google Patents

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JP2013184132A5
JP2013184132A5 JP2012052466A JP2012052466A JP2013184132A5 JP 2013184132 A5 JP2013184132 A5 JP 2013184132A5 JP 2012052466 A JP2012052466 A JP 2012052466A JP 2012052466 A JP2012052466 A JP 2012052466A JP 2013184132 A5 JP2013184132 A5 JP 2013184132A5
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activated carbon
activated
drying
spent
carbonate
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JP5792664B2 (en
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従来、スケールの組成分析法として、これら酸に難溶解性の金属酸化物の溶解には、アルカリ溶融法が採用されている。アルカリ溶融法は、そのアルカリ溶融生成物が、弱酸で容易に溶解できる。
酸化アルミニウム:Al23+アルカリ→Al2(OH)3、NaAlO2
酸化鉄:Fe23+アルカリ→Fe(OH)3
つまり、難溶解性の金属酸化物にアルカリ金属塩、主に炭酸ナトリウムと溶融することで、難溶解性の金属酸化物を酸に溶解しやすいアルカリ塩にできる。
また、炭酸ナトリウム、炭酸カリウムの融点は、それぞれ870℃、850℃であるが、炭酸ナトリウムと炭酸カリウムの等モル混合物の融点は780℃である。炭酸ナトリウムと炭酸カリウムの等モル混合物の融点が低いために低い温度でアルカリ溶融ができる。 本発明は前記の従来技術の課題を解決するために、鋭意研究の結果、考案されたものであり、吸着性能の高い使用済活性炭の再生方法、賦活活性炭およびその製造方法を提供するものである。
Conventionally, as a composition analysis method for a scale, an alkali melting method has been employed for dissolving a metal oxide that is hardly soluble in these acids. In the alkali melting method, the alkali molten product can be easily dissolved with a weak acid.
Aluminum oxide: Al 2 O 3 + alkali → Al 2 (OH) 3 , NaAlO 2
Iron oxide: Fe 2 O 3 + alkali → Fe (OH) 3
That is, by melting an alkali metal salt, mainly sodium carbonate, in a hardly soluble metal oxide, the hardly soluble metal oxide can be easily dissolved in an acid.
The melting points of sodium carbonate and potassium carbonate are 870 ° C. and 850 ° C., respectively, but the melting point of an equimolar mixture of sodium carbonate and potassium carbonate is 780 ° C. Since the melting point of an equimolar mixture of sodium carbonate and potassium carbonate is low, alkali melting can be performed at a low temperature. The present invention has been devised as a result of intensive studies to solve the above-described problems of the prior art, and provides a method for regenerating used activated carbon having high adsorption performance, an activated activated carbon, and a method for producing the same. .

1の発明は、水処理で使用した使用済活性炭を乾燥し、前記乾燥後の使用済活性炭を賦活再生し、前記賦活再生された賦活活性炭を酸洗浄・水洗いし、前記乾燥前または乾燥後の使用済活性炭に炭酸水素塩と、炭酸塩との少なくともいずれか一方を添加することで、再生炭を得ることを特徴とする使用済活性炭の再生方法である。
また、第1の発明は、前記乾燥前または乾燥後の使用済活性炭に、炭酸水素ナトリウムと炭酸水素カリウムとの混合物、または、炭酸ナトリウムと炭酸カリウムとの混合物、または、炭酸水素ナトリウムと炭酸カリウムとの混合物、または、炭酸ナトリウムと炭酸水素カリウムとの混合物を添加することが好ましい。
また、第1の発明は、前記使用済活性炭が高度浄水処理で使用されたものであることが好ましい。
第2の発明は、水処理で使用した使用済活性炭を乾燥する乾燥工程と、前記乾燥前または乾燥後の使用済活性炭に炭酸水素塩と、炭酸塩との少なくともいずれか一方を添加する添加工程と、前記乾燥後の使用済活性炭を賦活再生して賦活活性炭を得る賦活工程と、前記賦活再生された賦活活性炭を酸洗浄・水洗いする酸洗浄・水洗工程と、を備えたことを特徴とする賦活活性炭の製造方法である。
第3の発明は、第2の発明の前記賦活活性炭の製造方法によって得られることを特徴とする賦活活性炭である。
活性炭に捕捉された金属水酸化物は、賦活焼成での熱影響により金属酸化物にその形態が変化し、酸に難溶解性になる。
水酸化アルミニウム Al(OH) 3 → 酸化アルミニウム:Al 2 3
水酸化鉄 Fe(OH) 3 → 酸化鉄:Fe 2 3
二酸化マンガン MnO 2 (熱影響により酸による除去が困難になる)
つまり、賦活焼成前に、使用済活性炭に炭酸水素塩または炭酸塩を共存させることで賦活焼成での熱影響を受けて難溶解性の金属酸化物になるのを防止し、賦活焼成で酸に可溶の金属水酸化物または炭酸塩にする。
酸化アルミニウム:Al 2 3 +アルカリ→Al 2 (OH) 3 、NaAlO 2
酸化鉄:Fe 2 3 +アルカリ→Fe(OH) 3
二酸化マンガン:MnO 2 +アルカリ→Mn(OH) 4
The first invention, the spent activated carbon used in water treatment and dried, the spent activated carbon after drying was activated regeneration, the activated regenerated activated carbon was acid washed and washed with water, the drying before or after drying This is a method for regenerating used activated carbon, characterized in that regenerated charcoal is obtained by adding at least one of hydrogen carbonate and carbonate to the used activated carbon.
The first invention, the spent activated carbon before Symbol before drying or after drying, a mixture of sodium bicarbonate and potassium bicarbonate, or a mixture of sodium carbonate and potassium carbonate, or sodium bicarbonate and carbonate a mixture of potassium, or, preferably a benzalkonium be added a mixture of sodium carbonate and potassium hydrogen carbonate.
In the first invention, the used activated carbon is preferably used in advanced water purification treatment.
The second invention is a drying step of drying the used activated carbon used in the water treatment, and an addition step of adding at least one of a bicarbonate and a carbonate to the used activated carbon before or after the drying. When, characterized by comprising the activation step of obtaining the spent activated carbon activated reproduced by activated carbon after the drying, and a acid washing and water washing step of acid washing and water washing the activated regenerated activated carbon It is a manufacturing method of activated activated carbon.
3rd invention is the activated activated carbon characterized by being obtained by the manufacturing method of the said activated activated carbon of 2nd invention.
The form of the metal hydroxide trapped by the activated carbon is changed to a metal oxide due to the heat effect of the activation firing, and becomes hardly soluble in acid.
Aluminum hydroxide Al (OH) 3 → Aluminum oxide: Al 2 O 3
Iron hydroxide Fe (OH) 3 → Iron oxide: Fe 2 O 3
Manganese dioxide MnO 2 (It becomes difficult to remove by acid due to heat)
In other words, before activated firing, hydrogenated carbonate or carbonate is allowed to coexist with the used activated carbon to prevent it from becoming a hardly soluble metal oxide due to the heat effect of activated firing, and to the acid by activated firing. Soluble metal hydroxide or carbonate.
Aluminum oxide: Al 2 O 3 + alkali → Al 2 (OH) 3 , NaAlO 2
Iron oxide: Fe 2 O 3 + alkali → Fe (OH) 3
Manganese dioxide: MnO 2 + alkali → Mn (OH) 4

Claims (6)

水処理で使用した使用済活性炭を乾燥し
前記乾燥後の使用済活性炭を賦活再生し、
前記賦活再生された賦活活性炭を酸洗浄・水洗いし、
前記乾燥前または乾燥後の使用済活性炭に炭酸水素塩と、炭酸塩との少なくともいずれか一方を添加することで、再生炭を得ることを特徴とする使用済活性炭の再生方法。
Dry used activated carbon used in water treatment ,
Activated and regenerated used activated carbon after drying,
The activated activated carbon that has been activated and regenerated is washed with acid and washed with water,
The drying before or bicarbonate in the spent activated carbon after drying, by adding at least one of the carbonate method for regenerating spent activated carbon, characterized in that to obtain a reproduced charcoal.
前記請求項1記載において、
記乾燥前または乾燥後の使用済活性炭に、以下(1)〜(4)のいずれかを添加することを特徴とする使用済活性炭の再生方法。
(1)炭酸水素ナトリウムと炭酸水素カリウムとの混合
(2)炭酸ナトリウムと炭酸カリウムとの混合
(3)炭酸水素ナトリウムと炭酸カリウムとの混合
(4)炭酸ナトリウムと炭酸水素カリウムとの混合
In the claim 1,
Before Symbol the spent activated carbon after drying before or drying, the following (1) to a method of reproducing the spent activated carbon, characterized by the addition of either (4).
(1) A mixture of sodium bicarbonate and potassium bicarbonate
(2) Mixture of sodium carbonate and potassium carbonate
(3) A mixture of sodium bicarbonate and potassium carbonate
(4) Mixture of sodium carbonate and potassium bicarbonate
前記請求項1、2記載において、
前記使用済活性炭が高度浄水処理で使用されたものであることを特徴とする使用済活性炭の再生方法。
In Claims 1 and 2,
The method of reproducing the spent activated carbon, wherein the spent activated carbon is one that was used in the advanced water treatment.
水処理で使用した使用済活性炭を乾燥する乾燥工程と、
前記乾燥前または乾燥後の使用済活性炭に炭酸水素塩と、炭酸塩との少なくともいずれか一方を添加する添加工程と、
前記乾燥後の使用済活性炭を賦活再生して賦活活性炭を得る賦活工程と、
前記賦活再生された賦活活性炭を酸洗浄・水洗いする酸洗浄・水洗工程と、
備えたことを特徴とする賦活活性炭の製造方法。
A drying process for drying used activated carbon used in water treatment ;
The drying before or bicarbonate in the spent activated carbon after drying, the added step of adding at least one of the carbonate,
Activating and regenerating the activated carbon after drying to obtain activated activated carbon;
Acid cleaning / washing step of washing the activated activated carbon that has been activated and regenerated with water,
Method for producing activated carbon, characterized in that it comprises a.
前記請求項4記載において、
前記賦活工程と前記酸洗浄・水洗工程との間に有し、賦活再生された賦活活性炭を所定の粒度に調整する篩分工程と、
前記酸洗浄・水洗工程の後に有し、酸洗浄・水洗いされた賦活活性炭を乾燥する乾燥工程と、
を備えたことを特徴とする賦活活性炭の製造方法
In claim 4,
A sieving step for adjusting the activated activated carbon that has been activated and regenerated to have a predetermined particle size between the activation step and the acid washing / water washing step,
After the acid washing / water washing step, a drying step for drying the activated activated carbon that has been acid washed / water washed,
A method for producing activated activated carbon, comprising:
前記請求項4、5記載において、
前記賦活活性炭の製造方法によって得られることを特徴とする賦活活性炭。
In the said Claim 4 , 5,
An activated activated carbon obtained by the method for producing an activated activated carbon.
JP2012052466A 2012-03-09 2012-03-09 Method for regenerating used activated carbon, activated activated carbon and method for producing the same Active JP5792664B2 (en)

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JP6165598B2 (en) * 2013-11-13 2017-07-19 水ing株式会社 Regeneration method of plant-based spherical activated carbon and reuse method of the regenerated plant-based spherical activated carbon in water purification treatment
CN107473473A (en) * 2017-10-10 2017-12-15 丁玉琴 A kind of household water purifier
CN111889089A (en) * 2020-05-12 2020-11-06 天津天一爱拓科技有限公司 System and method for regenerating waste activated carbon
CN115121235B (en) * 2021-03-29 2023-11-17 湖南大学 Regeneration and utilization method of edible tree fungus charcoal for adsorbing heavy metals
CN115193428A (en) * 2021-04-14 2022-10-18 上海交通大学 Regeneration method of waste activated carbon containing perfluorinated compounds
CN113231017B (en) * 2021-04-29 2023-07-18 广东工业大学 Modified superfine powder activated carbon and preparation method and application thereof
CN114804104A (en) * 2022-02-21 2022-07-29 江苏联兴成套设备制造有限公司 Organic fermentation reinforced CO 2 Method for regenerating waste active carbon by activating pore-forming
CN114634722A (en) * 2022-04-06 2022-06-17 安徽固瑞特新材料科技有限公司 Method for improving structure of regenerated carbon black
CN115970667B (en) * 2023-02-22 2024-03-19 成都华域环保有限公司 Regeneration method of waste powdery activated carbon
CN116282328B (en) * 2023-02-27 2023-10-13 中国科学院生态环境研究中心 Method for efficiently regenerating mineralized synergistic activated carbon by catalyzing perfluorinated compounds at low temperature

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ZA785864B (en) * 1978-10-18 1979-12-27 Anglo Amer Corp South Africa Regeneration of activated carbon
JPH09225260A (en) * 1996-02-20 1997-09-02 Ebara Corp Regenerating method of activated carbon based material
JP2005034742A (en) * 2003-07-15 2005-02-10 Ebara Engineering Service Co Ltd Method for treating spent carbon and usage of the carbon
JP3746509B1 (en) * 2004-08-20 2006-02-15 日本エンバイロケミカルズ株式会社 Spherical activated carbon and its manufacturing method

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