JPS62283866A - Manufacture of active carbon formed body - Google Patents
Manufacture of active carbon formed bodyInfo
- Publication number
- JPS62283866A JPS62283866A JP61124509A JP12450986A JPS62283866A JP S62283866 A JPS62283866 A JP S62283866A JP 61124509 A JP61124509 A JP 61124509A JP 12450986 A JP12450986 A JP 12450986A JP S62283866 A JPS62283866 A JP S62283866A
- Authority
- JP
- Japan
- Prior art keywords
- activated carbon
- temperature
- organic binder
- starts
- substance
- 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
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims description 99
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 229910052799 carbon Inorganic materials 0.000 title description 2
- 239000000126 substance Substances 0.000 claims description 26
- 239000011230 binding agent Substances 0.000 claims description 17
- 238000010304 firing Methods 0.000 claims description 7
- 238000004898 kneading Methods 0.000 claims description 5
- 238000000354 decomposition reaction Methods 0.000 claims description 4
- 238000003763 carbonization Methods 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- 239000002245 particle Substances 0.000 description 5
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- -1 baladichlorobenzene Chemical compound 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000004801 Chlorinated PVC Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229960000846 camphor Drugs 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 229920000457 chlorinated polyvinyl chloride Polymers 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000007849 furan resin Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
Landscapes
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Ceramic Products (AREA)
- Carbon And Carbon Compounds (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
5、 発明の詳細な説明
(産業上の利用分野)
例えば、電池電極のような解媒担体やフィルターなどに
用いられる活性炭成形物の製造方法に関する。目的は、
吸着能や触媒能など活性炭機能の発揮を十分になさしめ
ることである。Detailed Description of the Invention 5. Detailed Description of the Invention (Industrial Field of Application) For example, the present invention relates to a method for manufacturing an activated carbon molded product used for a dissolving medium carrier such as a battery electrode, a filter, and the like. My goal is,
The goal is to allow activated carbon to fully demonstrate its functions such as adsorption and catalytic abilities.
有機結合材を活性炭および必要に応じて使用される他の
材料とともに混練し、焼成処理を施すことによって活性
炭成形物を製造している。焼成による有機結合材の炭化
時に自ずと形成される微細気孔が分散含有される活性炭
への気体通路として使用される訳である。Activated carbon molded articles are manufactured by kneading the organic binder with activated carbon and other materials used as necessary, and subjecting the mixture to a firing treatment. The fine pores that are naturally formed when the organic binder is carbonized by firing are used as gas passages to the activated carbon that is dispersed therein.
しかし、活性炭表面上が炭素骨格で覆われてしまうため
であろうと思われるが、十分′な活性炭機能を得ること
が難しい。However, it is difficult to obtain a sufficient activated carbon function, probably because the surface of the activated carbon is covered with a carbon skeleton.
そこで2本願出願人は活性炭を解重合型有機物で予め被
覆したものを使用することによってこの問題を大きく改
善するという出願を前になした(特開昭60−2046
10号)。Therefore, the applicant of the present application previously filed an application to greatly improve this problem by using activated carbon coated in advance with a depolymerizable organic substance (Japanese Unexamined Patent Publication No. 60-2046).
No. 10).
これを更により大きな効果を奏し得るようにしたのが本
発明である。The present invention makes it possible to achieve even greater effects.
(問題点を解決するための手段)
本発明は、焼成により炭化する有機結合材と活性炭とを
少なくとも主材として使用し、混線後、焼成して活性炭
成形物を製造するにあたり。(Means for Solving the Problems) The present invention uses an organic binder that carbonizes when fired and activated carbon as at least the main materials, and after cross-wiring, fires to produce an activated carbon molded product.
混練前の前記活性炭を、前記有機結合材が分解炭化開始
する温度以下で昇華開始する昇華性物質で予め含浸して
おき、さらに、その表面を前記有機結合材の分解炭化開
始する温度以上で気散する解重合型有機物で被覆したこ
とを特徴とする活性炭成形物の製造方法を要旨とする。The activated carbon before kneading is impregnated in advance with a sublimating substance that starts to sublimate at a temperature below the temperature at which the organic binder starts to decompose and carbonize, and the surface is further impregnated with air at a temperature above the temperature at which the organic binder starts to decompose and carbonize. The gist of the present invention is a method for producing an activated carbon molded article, which is characterized by being coated with a depolymerizable organic substance that is dispersed in the activated carbon.
以下詳述する。The details will be explained below.
有機結合材としては、天然1合成の樹脂、ゴム、熱硬化
性初期縮合体、ピッチ、タール、アスファルトなど種々
の選択対象があり、−例としては、スチロール樹脂、ア
クリル樹脂、尿素樹脂、メラミン樹脂、ポリエステル樹
脂、フラン樹脂、ポリビニルアルコール、ポリアクリル
アミド、ブチルゴム、塩素化ポリ塩化ビニル。There are a variety of organic binders to choose from, including natural and synthetic resins, rubber, thermosetting precondensates, pitch, tar, and asphalt; examples include styrene resin, acrylic resin, urea resin, and melamine resin. , polyester resin, furan resin, polyvinyl alcohol, polyacrylamide, butyl rubber, chlorinated polyvinyl chloride.
塩素化ポリエチレン、ポリ塩化ビニルなど挙げられ、適
宜1種もしくけ2種以上組み合わせて使用することがで
きる。Examples include chlorinated polyethylene and polyvinyl chloride, and they can be used alone or in combination of two or more.
活性炭としては、原材料や製法などによらず適宜使用で
き2粒径も特に限定されない。但し。As activated carbon, it can be used as appropriate regardless of raw materials, manufacturing method, etc., and the particle size is not particularly limited. however.
あまり粒径が大きいと成形物の強度を損う原因にもなり
かねないので、望ましくは100μm以下のものを使用
する。If the particle size is too large, it may cause a loss in the strength of the molded product, so it is preferable to use particles with a particle size of 100 μm or less.
活性炭に含浸させる昇華性物質としては、有機結合材の
分解炭化開始する温度以下で昇華開始するものを選択す
る。−例としては、ナフタリン、ショウノウ、バラジク
ロルベンゼン、ヨウ素などである。As the sublimable substance to be impregnated into the activated carbon, one is selected that starts to sublimate at a temperature below the temperature at which decomposition and carbonization of the organic binder starts. - Examples are naphthalene, camphor, baladichlorobenzene, iodine, etc.
活性炭に昇華性物質を含浸させる方法としては、昇華性
物質を溶剤等に溶解させた溶液に活性炭を浸漬させたり
、加熱浸漬や真空含浸させたりする一般に知られている
方法を用いることができる。As a method for impregnating activated carbon with a sublimable substance, generally known methods such as immersing activated carbon in a solution of a sublimable substance dissolved in a solvent, heating immersion, or vacuum impregnation can be used.
活性炭表面を被覆する解重合型有機物としては、有機結
合材が分解炭化開始する温度以上で気散するものを選択
する。−例としては、ポリエチレン、ホ゛リプロピレン
、ポリブタジェン。As the depolymerizable organic substance that coats the surface of the activated carbon, one is selected that vaporizes at a temperature higher than the temperature at which the organic binder starts to decompose and carbonize. - Examples are polyethylene, polypropylene, polybutadiene.
ポリイソブチレン、ポリスチレン、ナイロン。Polyisobutylene, polystyrene, nylon.
ポリメタメチルスチレン、ポリメタクリル酸メチル、ポ
リエタクリル酸エチル、ピリ−α−トイテロスチレンな
どである。天然ゴムの中にも解重合型のものがある。こ
れらの中で特に好ましいのはポリメタクリル酸メチルで
あり、解重合の程度が極めて高1ρ。These include polymethmethylstyrene, polymethyl methacrylate, polyethyl ethacrylate, pyri-α-toiterostyrene, and the like. There are also depolymerized types of natural rubber. Particularly preferred among these is polymethyl methacrylate, which exhibits an extremely high degree of depolymerization.
解重合型有機物質による活性炭の表面被覆方法は、エマ
ルジョンやサスペンションにしてなす方法とか粉床法な
どマイクロカプセルの製造方法として公知の種々方法を
採用することもできるが、最も簡単と思われるのは、可
塑剤や溶剤などを必要に応じて使用しながら混練するこ
とである。使用量の相対的割合が容易に変化できる長所
もある。To coat the surface of activated carbon with a depolymerized organic substance, various methods known for producing microcapsules can be adopted, such as emulsion or suspension methods, powder bed methods, etc., but the easiest method is considered to be , kneading, using plasticizers, solvents, etc. as necessary. Another advantage is that the relative proportions of usage can be easily changed.
このようにして得られた活性炭を有機結合材や必要に応
じて使用される安定剤、溶剤、黒鉛などとともにニーダ
−23本ロールなどで混練する。これを、板状2円柱状
、ハニカム状など所望の形状に成形し、更に必要に応じ
て乾燥後。The activated carbon thus obtained is kneaded with an organic binder and optionally used stabilizers, solvents, graphite, etc. using a kneader with 23 rolls or the like. This is formed into a desired shape such as a plate, two cylinders, or a honeycomb shape, and further dried if necessary.
焼成の熱処理を施して有機結合材を炭化させる。The organic binder is carbonized by heat treatment of firing.
このとき、活性炭中に含浸させた昇華性物質や表面に被
覆した解重合型有機物が気散する際に。At this time, when the sublimable substance impregnated into the activated carbon and the depolymerizable organic substance coated on the surface are diffused.
急速な昇温速度では成形物の割れや脹れなどを生じる可
能性もあるので、十分考慮して昇温速度を決めることが
望ましい。たとえば有機結合材としてポリ塩化ビニルを
使用した場合は、グレードなどによっても異なるが、1
30°Cから300°Cくらいの範囲の昇温速度を毎分
5°Cとか2℃とかいったようにするとよい。また、焼
成は、不活性ガス雰囲気、還元雰囲気、真空雰囲気とい
った適宜の非酸化性雰囲気で行なうことができ2通常、
最高温度は600℃〜900°C程度である。A rapid temperature increase rate may cause cracking or swelling of the molded product, so it is desirable to decide the temperature increase rate with due consideration. For example, when polyvinyl chloride is used as an organic binder, it varies depending on the grade, etc.
It is recommended that the temperature increase rate be 5°C or 2°C per minute in the range from 30°C to 300°C. Further, the firing can be carried out in an appropriate non-oxidizing atmosphere such as an inert gas atmosphere, a reducing atmosphere, or a vacuum atmosphere.2 Usually,
The maximum temperature is about 600°C to 900°C.
焼成後、更に必要に応じて賦活処理を施して活性炭成形
物を得る。After firing, an activation treatment is further performed as necessary to obtain an activated carbon molded product.
(作用)
活性炭に含浸された昇華性物質は、有機結合材が分解炭
化開始する温度以下で昇華開始するため、微細孔まで含
浸されていても容易に気散する。この状態で、活性炭の
表面には、有機結合材の分解炭化開始する温度以上で気
散する解重合型有機物が被覆している。つまり、空とな
った細孔、特に微細孔部が有機結合材の炭化物に塞がれ
ることなく確保されている。そして。(Function) Since the sublimable substance impregnated into the activated carbon starts sublimating at a temperature below the temperature at which the organic binder starts to decompose and carbonize, it easily evaporates even if it is impregnated to the minute pores. In this state, the surface of the activated carbon is coated with a depolymerizable organic substance that evaporates at a temperature higher than the temperature at which decomposition and carbonization of the organic binder starts. In other words, empty pores, especially micropores, are secured without being blocked by the carbide of the organic binder. and.
解重合型有機物の分解により発生したガスの抜は道が連
通気孔として残ることになる。このとき、解重合型有機
物が活性炭細孔に残存することはまずない。しかも、こ
の連通気孔は、活性炭の内部とつながる。かように本発
明者は推察している。The gas generated by the decomposition of the depolymerized organic matter is vented, leaving a path as a continuous vent. At this time, it is unlikely that depolymerized organic substances remain in the activated carbon pores. Moreover, this communicating hole is connected to the inside of the activated carbon. This is what the inventor of the present invention conjectures.
(実施例) 以下単に部とあるのは重量部を示す。(Example) Hereinafter, parts simply refer to parts by weight.
〔実施例1〕
(1) 昇華性物質含浸解重合型有機物被覆活性炭の
準備
ナフタリンとメチルエチルケトンとを1:5に調製した
溶液に日次Y(日立炭素工業■製の粉末活性炭二粒径1
50メソシュ以下)50部を浸漬し、約30分放置して
活性炭中に溶液を十分に含浸させた。溶液から取り出し
た活性炭をメチルエチルケトン除去のため速やかに乾燥
した後、アクリシラ、プ5Y−103(三菱レイヨン■
製のポリメタクリル酸メチル)とメチルエチルケトンを
1=2に調製した溶液に浸漬し。[Example 1] (1) Preparation of activated carbon coated with a depolymerizable organic substance impregnated with a sublimable substance.
50 parts (50 mesosh or less) was immersed and left to stand for about 30 minutes to fully impregnate the solution into the activated carbon. After quickly drying the activated carbon taken out from the solution to remove methyl ethyl ketone,
Polymethyl methacrylate) and methyl ethyl ketone were immersed in a solution prepared in a ratio of 1=2.
約10分放置後、取出し、活性炭表面にアクリシラツブ
5Y−103を被覆させた。After being left for about 10 minutes, it was taken out and the activated carbon surface was coated with Acrysilab 5Y-103.
得たものは75部あった。I got 75 copies.
(2) 活性炭成形物の製造
(1)で準備した活性炭 75部ポリ塩化
ビニル樹脂 30部ジオクチルフタレート
(可塑剤) 15部ステアリン酸塩(安定剤)
2部黒 鉛
20部メチルエチルケトン
20部上記配合物をニーダで15分間混練後、押出成形
して直径約1mmの棒状成形物を得た。(2) Manufacture of activated carbon molded product Activated carbon prepared in (1) 75 parts Polyvinyl chloride resin 30 parts Dioctyl phthalate (plasticizer) 15 parts Stearate (stabilizer)
Part 2 graphite
20 parts methyl ethyl ketone
20 parts of the above blend was kneaded in a kneader for 15 minutes and then extruded to obtain a rod-shaped molded product with a diameter of about 1 mm.
これを空気中で室温から300°Cまで2°C/分程度
の昇温速度で加熱した後、密閉容器中で850℃、1時
間の焼成処理を施して活性炭成形物を得た。This was heated in air from room temperature to 300°C at a rate of temperature increase of about 2°C/min, and then fired in a closed container at 850°C for 1 hour to obtain an activated carbon molded article.
〔実施例2〕
実施例1において1白炭Yに代えて粉末炭PW(クラレ
ケミカル■製の粉末活性炭:粒径200メ、シュ以下)
を使用した以外、すべて実施例1と同様にした。[Example 2] In Example 1, instead of white charcoal Y, powdered carbon PW (powdered activated carbon manufactured by Kuraray Chemical ■: particle size of 200 mm or less) was used.
Everything was the same as in Example 1 except that .
〔実施例3〕
実施例1において、ナフタリンに代えてdi−ショウノ
ウを使用した以外、すべて実施例1と同様にした。[Example 3] Everything was the same as in Example 1 except that di-camphor was used in place of naphthalene.
〔比較例1,2〕
実施例1の(2)、2の(2)において、昇華性物質含
浸解重合型有機物被覆処理した活性炭75部に代えて昇
華性物質含浸処理のみした活性炭(処理前活性炭50部
)を使用した以外、すべて実施例1,2と同様にした。[Comparative Examples 1 and 2] In Example 1 (2) and 2 (2), instead of 75 parts of activated carbon impregnated with a sublimable substance and coated with a depolymerizable organic substance, activated carbon impregnated with a sublimable substance (before treatment) was used. The same procedure as in Examples 1 and 2 was carried out except that 50 parts of activated carbon was used.
〔比較例3,4〕
実施例1の(2)、2の(2)において、昇華性物質含
浸解重合型有機物被覆処理した活性炭75部に代えて解
重合型有機物被覆のみした活性炭(処理前活性炭50部
)を使用した以外、すべて実施例1.2と同様にした。[Comparative Examples 3 and 4] In Example 1 (2) and 2 (2), instead of 75 parts of activated carbon impregnated with a sublimable substance and coated with a depolymerizable organic substance, activated carbon coated with a depolymerizable organic substance (before treatment) was used. Everything was the same as in Example 1.2 except that 50 parts of activated carbon) was used.
〔比較例5,6〕
実施例1の(2)、2の(2)において、昇華性物質含
浸解重合型有機物被覆処理した活性炭75部に代えて何
ら処理しない活性炭50部を使用した以外、すべて実施
例1,2と同様にした。[Comparative Examples 5 and 6] In Examples 1-(2) and 2-(2), 50 parts of activated carbon without any treatment was used instead of 75 parts of activated carbon impregnated with a sublimable substance and coated with a depolymerizable organic substance. All procedures were carried out in the same manner as in Examples 1 and 2.
(発明の効果) 各側で得たものについての評価結果を表−1に示す。(Effect of the invention) Table 1 shows the evaluation results obtained on each side.
尚1強度はJIS S 6005に準じ、比表面積けB
ET法により測定した。In addition, 1 strength is based on JIS S 6005, specific surface area B
Measured by ET method.
表−1
この表−1より判るように1本発明によれば活性炭機能
に優れた活性炭成形物を得ることができる。Table 1 As can be seen from Table 1, according to the present invention, an activated carbon molded product having excellent activated carbon function can be obtained.
Claims (1)
も主材として使用し、混練後、焼成して活性炭成形物を
製造するにあたり、混練前の前記活性炭を、前記有機結
合材が分解炭化開始する温度以下で昇華開始する昇華性
物質で予め含浸しておき、さらに、その表面を前記有機
結合材の分解炭化開始する温度以上で気散する解重合型
有機物で被覆したことを特徴とする活性炭成形物の製造
方法。When producing an activated carbon molded product by using at least an organic binder that carbonizes by firing and activated carbon as the main materials and firing after kneading, the activated carbon before kneading is heated to a temperature below the temperature at which the organic binder starts to decompose and carbonize. An activated carbon molded article characterized in that it has been impregnated in advance with a sublimable substance that starts to sublimate at , and its surface is further coated with a depolymerizable organic substance that evaporates at a temperature higher than the temperature at which decomposition and carbonization of the organic binder starts. Production method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61124509A JPS62283866A (en) | 1986-05-29 | 1986-05-29 | Manufacture of active carbon formed body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61124509A JPS62283866A (en) | 1986-05-29 | 1986-05-29 | Manufacture of active carbon formed body |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62283866A true JPS62283866A (en) | 1987-12-09 |
Family
ID=14887245
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61124509A Pending JPS62283866A (en) | 1986-05-29 | 1986-05-29 | Manufacture of active carbon formed body |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62283866A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008136982A (en) * | 2006-12-05 | 2008-06-19 | Chiyoda Corp | Carbon-based catalyst for flue-gas desulfurization and its manufacturing method |
-
1986
- 1986-05-29 JP JP61124509A patent/JPS62283866A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008136982A (en) * | 2006-12-05 | 2008-06-19 | Chiyoda Corp | Carbon-based catalyst for flue-gas desulfurization and its manufacturing method |
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