JPH038440A - Adsorbent for oil mist - Google Patents
Adsorbent for oil mistInfo
- Publication number
- JPH038440A JPH038440A JP14347489A JP14347489A JPH038440A JP H038440 A JPH038440 A JP H038440A JP 14347489 A JP14347489 A JP 14347489A JP 14347489 A JP14347489 A JP 14347489A JP H038440 A JPH038440 A JP H038440A
- Authority
- JP
- Japan
- Prior art keywords
- oil mist
- pellets
- carbon
- adsorbent
- black
- 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
- 239000003595 mist Substances 0.000 title claims abstract description 22
- 239000003463 adsorbent Substances 0.000 title claims description 17
- 239000011148 porous material Substances 0.000 claims abstract description 24
- 239000008188 pellet Substances 0.000 claims abstract description 15
- 239000006229 carbon black Substances 0.000 claims abstract description 12
- 229910021397 glassy carbon Inorganic materials 0.000 claims abstract description 9
- 239000002344 surface layer Substances 0.000 claims abstract description 6
- 238000009826 distribution Methods 0.000 claims description 6
- 238000005259 measurement Methods 0.000 claims description 4
- 238000010586 diagram Methods 0.000 claims description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 3
- 229910052753 mercury Inorganic materials 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 29
- 239000011347 resin Substances 0.000 abstract description 13
- 229920005989 resin Polymers 0.000 abstract description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract description 4
- 239000010410 layer Substances 0.000 abstract description 4
- 239000002904 solvent Substances 0.000 abstract description 4
- 229920001187 thermosetting polymer Polymers 0.000 abstract description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract description 2
- 238000003763 carbonization Methods 0.000 abstract description 2
- 238000010304 firing Methods 0.000 abstract description 2
- 239000007849 furan resin Substances 0.000 abstract 1
- 239000005011 phenolic resin Substances 0.000 abstract 1
- 238000001179 sorption measurement Methods 0.000 description 16
- 229910052799 carbon Inorganic materials 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003575 carbonaceous material Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000006231 channel black Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000006234 thermal black Substances 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、各種オイルミスト(油蒸気)の吸着除去に用
いられるオイルミスト用吸着材に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an oil mist adsorbent used for adsorption and removal of various oil mist (oil vapor).
オイルミスト用の吸着材には、ステンレス鋼、アルミナ
、ガラスなどの繊維を編組したフェルト状のものが市販
されている。ところが、これらの材料は高価格であるう
え、施工時に短繊維となって飛散するなど取扱い面に問
題がある。Felt-like adsorbents made of braided fibers of stainless steel, alumina, glass, etc. are commercially available as adsorbents for oil mist. However, these materials are expensive and have problems in handling, such as becoming short fibers and scattering during construction.
この点、従来から気相/液相用の吸着材として汎用され
ている石炭系、ヤシガラ系などの粒状活性炭は価格およ
び取扱いの両面において有利である。しかしながら、活
性炭はガス、蒸気等の気相吸着には優れた除去性能を発
揮するものの、オイルミストのような微小液相粒子に対
しては十分な吸着効果を示さない難点がある。In this respect, granular activated carbon such as coal-based or coconut shell-based activated carbon, which has been widely used as an adsorbent for gas/liquid phases, is advantageous in terms of both price and handling. However, although activated carbon exhibits excellent removal performance for vapor phase adsorption of gases, vapors, etc., it has the disadvantage that it does not exhibit sufficient adsorption effects for minute liquid phase particles such as oil mist.
活性炭がオイルミストに対して十分な吸着性能を発揮し
ない理由は、その気孔構造が主に窒素吸着比表面積(N
!SA) 1000 rrr/g以上の比表面積で代表
される高いミクロボアーで構成されており、オイルミス
トの吸着に必要とされる微細孔容積(nm以上の微細孔
)が少ないためである。The reason why activated carbon does not exhibit sufficient adsorption performance for oil mist is that its pore structure mainly has a nitrogen adsorption specific surface area (N
! SA) It is composed of high micropores represented by a specific surface area of 1000 rrr/g or more, and the micropore volume (micropores of nm or more) required for oil mist adsorption is small.
本発明は、活性炭とは異なる組織構造をもつカーボンブ
ラック表層部にガラス状炭素被膜を形成した炭素賞球状
体が微細孔容積を多く保存し、そのほかオイルミストの
吸着に有効な特性を備えていることを知見して開発に至
ったものである。In the present invention, carbon spherical bodies with a glassy carbon film formed on the surface layer of carbon black, which has a different structure from activated carbon, preserve a large volume of micropores and have other properties that are effective in adsorbing oil mist. This was developed based on this knowledge.
したがって、本発明の目的は、オイルミストを効果的に
吸着することができる炭素質吸着材を提供するところに
ある。Therefore, an object of the present invention is to provide a carbonaceous adsorbent that can effectively adsorb oil mist.
(課題を解決するための手段)
上記の目的を達成するための本発明の係にオイルミスト
用吸着材は、カーボンブラックベレットの表層部にガラ
ス状炭素を被着形成した炭素質球状体であって、水銀ポ
ロシメーターによる細孔分布測定において、全細孔容積
が0.4 tying以上、細孔分布図から算出される
平均細孔径が20nl11以上の特性を有してなること
を構成上の特徴とする。(Means for Solving the Problems) To achieve the above object, an oil mist adsorbent is a carbonaceous spherical body formed by adhering glassy carbon to the surface layer of a carbon black pellet. In the pore distribution measurement using a mercury porosimeter, the structural feature is that the total pore volume is 0.4 tying or more and the average pore diameter calculated from the pore distribution diagram is 20 nl11 or more. do.
本発明の炭素質球状体は、次のようにして製造される。The carbonaceous spherical bodies of the present invention are manufactured as follows.
まず、熱硬化性樹脂を適宜な有機溶媒に溶解してカーボ
ンブラックペレットに含浸したのち加熱処理する。First, a thermosetting resin is dissolved in an appropriate organic solvent and impregnated into carbon black pellets, followed by heat treatment.
カーボンブラックとしては、オイルファーネスブラック
、ガスファーネスブラック、チャンネルブラック、サー
マルブラック、アセチレンブラック、ランプブラック、
副生ブラックなど各種製造系統のものが適用でき、常用
の造粒手段により球状のペレットに形成して使用に供さ
れる。Carbon black includes oil furnace black, gas furnace black, channel black, thermal black, acetylene black, lamp black,
Various production systems such as by-product black can be used, and the product is formed into spherical pellets by conventional granulation means and used.
熱硬化性樹脂には、炭化処理によってガラス状炭素に転
化しやすいフェノール系あるいはフラン系のものが有用
され、アルコール、エーテル、アセトン、ベンゼン、ト
ルエン、キシレンなど揮発性の有機溶媒に溶解した状態
で用いられる。Phenol-based or furan-based thermosetting resins that are easily converted into glassy carbon by carbonization are useful, and they can be dissolved in volatile organic solvents such as alcohol, ether, acetone, benzene, toluene, and xylene. used.
含浸処理は、例えばカラム中にカーボンブランクペレッ
トを充填して樹脂溶液を流下する方法、回転円筒管中で
カーボンブラックベレットを転勤させながら樹脂溶液を
噴霧する方法あるいは樹脂溶液中にカーボンブランクベ
レットを浸漬する方法等の手段を用いておこなわれる。The impregnation treatment can be carried out, for example, by filling a column with carbon blank pellets and letting the resin solution flow down, by spraying the resin solution while transferring the carbon black pellets in a rotating cylindrical tube, or by immersing the carbon blank pellets in the resin solution. This is done using methods such as
これらの方法でカーボンブラックペレットに含浸した樹
脂溶液は、その一部がペレット内部に浸透するが、加熱
時の溶媒連敗に伴って表層部に移行して被着状態で固定
化される。A portion of the resin solution impregnated into the carbon black pellets by these methods penetrates into the inside of the pellets, but as the solvent continues to fail during heating, it migrates to the surface layer and is fixed in an adhered state.
ついで、これを非酸化性雰囲気中1500〜2000°
C程度の温度域で焼成炭化すると樹脂層部分はガラス状
炭素に転化し、カーボンブラックペレットの表層部にガ
ラス状炭素が被着形成した炭素質球状体が得られる。Next, this was heated at 1500 to 2000° in a non-oxidizing atmosphere.
When carbonized by firing in a temperature range of approximately C, the resin layer portion is converted to glassy carbon, and a carbonaceous spherical body in which glassy carbon is adhered to the surface layer of carbon black pellets is obtained.
本発明の吸着材は、上記の炭素賞球体であるうえに、水
銀ポロシメーターによる細孔分布測定において全細孔容
積が0.4 tall/g以上、また細孔分布図から算
出される平均細孔径が20nm以上の特性を保有するこ
とが要件となるもので、この要件を満足しないとオイル
ミストに対する十分な吸着性能を付与することができな
くなる。The adsorbent of the present invention is not only the above-mentioned carbon sphere, but also has a total pore volume of 0.4 tall/g or more in pore distribution measurement using a mercury porosimeter, and an average pore diameter calculated from a pore distribution diagram. is required to have a characteristic of 20 nm or more, and if this requirement is not satisfied, sufficient adsorption performance for oil mist cannot be imparted.
これら細孔構造特性は上記した炭素質球状体の製造条件
を制御することで付与することができるが、主に原料に
用いるカーボンブラックの細孔特性に支配される要素が
大きい。These pore structure characteristics can be imparted by controlling the manufacturing conditions of the carbonaceous spheres described above, but they are largely influenced by the pore characteristics of the carbon black used as the raw material.
本発明によるオイルミスト用吸着材は、性状として炭素
分99%を越える高純度性と安息角30°程度の真球性
に富む炭素質物であり、かつオイルミストの吸着に好適
な全細孔容積0.4 af/g以上および平均細孔径2
0nn以上の細孔構造特性を備えている。The adsorbent for oil mist according to the present invention is a carbonaceous material with high purity with a carbon content of over 99% and sphericity with an angle of repose of about 30°, and has a total pore volume suitable for oil mist adsorption. 0.4 af/g or more and average pore diameter 2
It has a pore structure characteristic of 0 nn or more.
オイルミストの吸着にあたっては、まず高純度特性がオ
イルミストとの濡れ性を改善するために寄与し、真球性
はカラムなどへの充填・排出に際しての作業性を円滑化
するとともにオイルミスト含有ガスとの接触を良好にす
る作用を営む。これらの作用が全細孔容積0.4 m7
g以上および平均細孔径20nm以上に基づく吸着性能
と相俟って吸着効果を一層高めるために機能する。When adsorbing oil mist, firstly, high purity properties contribute to improving wettability with oil mist, and sphericity facilitates workability when filling and discharging columns etc. It acts to improve contact with the These actions reduce the total pore volume to 0.4 m7
Together with the adsorption performance based on g or more and an average pore diameter of 20 nm or more, it functions to further enhance the adsorption effect.
以下、本発明を実施例により説明する。 The present invention will be explained below with reference to Examples.
(1)吸着材の製造
2種類のカーボンブランク〔実施例1:東海カーボン■
製”5EAS↑116”、実施例2:東海カーボン■製
“5EAST 9”〕を湿式造粒したペレットを篩分け
して、直径0.5〜2.0踵の粒度範囲を採取した。こ
のカーボンブラックベレットを回転円筒管に入れ、フラ
ン樹脂〔日立化成■製“ヒタフランVF303”〕の2
.5%アセトン溶液を噴霧しながらlQrpmの速度で
回転して均一に含浸させた。(1) Production of adsorbent Two types of carbon blanks [Example 1: Tokai Carbon ■
"5EAS↑116" manufactured by Tokai Carbon Corporation, Example 2: "5EAST 9" manufactured by Tokai Carbon ■] were sieved to collect particles in the particle size range of 0.5 to 2.0 diameter. This carbon black pellet was placed in a rotating cylindrical tube, and 2
.. While spraying a 5% acetone solution, it was rotated at a speed of 1 Qrpm to uniformly impregnate it.
引続き、転勤させながら加熱して溶媒成分を揮散させ、
樹脂層を硬化した。Next, heat the solvent while transferring it to volatilize the solvent component,
The resin layer was cured.
硬化処理後の粒体は、窒素ガス雰囲気炉で1500°C
の温度に30分保持して樹脂成分を焼成炭化した。After the hardening treatment, the granules are heated at 1500°C in a nitrogen gas atmosphere furnace.
The resin component was fired and carbonized by holding the resin at a temperature of 30 minutes.
このようにして作成した炭素質吸着材は、内部にカーブ
ンブラックを封入し外層が強固かつ平滑なガラス状炭素
被膜を有する極めて真球に近い性状を呈しており、その
元素分析値はC:99%、H: 0.05%以下、N:
Q、1%、O:O,X%と高純変炭素質であることが確
認された。The carbonaceous adsorbent created in this way exhibits properties that are extremely close to a perfect sphere, with carbune black sealed inside and a strong and smooth glassy carbon coating on the outer layer, and its elemental analysis value is C: 99%, H: 0.05% or less, N:
It was confirmed that it was a highly pure modified carbonaceous material with a content of Q: 1% and O:O:X%.
(2)オイルミスト吸着性能の評価
内径60m、外径70■のアクリル樹脂製円筒カラムに
吸着材を充填し、両端部をステンレス網で固定した。こ
の際の吸着材充填条件は、充填150g、かさ密度0.
31g/cc、粒度2000〜250 tttsに設定
した。市販の真空ポンプの排気管に上記の吸着材充填カ
ラムを接続して駆動させ、吸着量の経時変化を測定した
。なお、オイルミスト発生量の制御は吸引側のガス量を
調節することによりおこなった。(2) Evaluation of oil mist adsorption performance An acrylic resin cylindrical column with an inner diameter of 60 m and an outer diameter of 70 cm was filled with adsorbent, and both ends were fixed with stainless steel nets. The adsorbent filling conditions at this time were: filling 150g, bulk density 0.
The particle size was set at 31 g/cc and a particle size of 2000 to 250 ttts. The above-mentioned adsorbent-filled column was connected to the exhaust pipe of a commercially available vacuum pump and driven, and changes in adsorption amount over time were measured. The amount of oil mist generated was controlled by adjusting the amount of gas on the suction side.
(3)吸着結果
上記のようにして評価した吸着性能の測定結果を、吸着
材の特性と対比させて第1表に示した。(3) Adsorption Results The measurement results of the adsorption performance evaluated as described above are shown in Table 1 in comparison with the characteristics of the adsorbent.
なお、比較のために市販の石炭系球状活性炭について評
価した結果も併せて示した(比較例)。For comparison, the results of evaluating commercially available coal-based spherical activated carbon are also shown (comparative example).
本発明の実施例は比較例に比べ長時間に亘って安定した
オイルミストの吸着性能を維持しており、とくに細孔容
積および平均細孔径の大きい実施例1において高性能を
示すことが認められた。The Examples of the present invention maintained stable oil mist adsorption performance over a long period of time compared to the Comparative Examples, and it was observed that Example 1, which had a large pore volume and average pore diameter, exhibited particularly high performance. Ta.
以上のとおり、本発明によれば安価で取扱いの良好な炭
素質材料により優れた吸着性能を有するオイルミスト用
吸着材を提供することができるから、工業的に資すると
ころ大である。As described above, according to the present invention, it is possible to provide an oil mist adsorbent having excellent adsorption performance using a carbonaceous material that is inexpensive and easy to handle, so it is of great industrial benefit.
Claims (1)
を被着形成した炭素質球状体であって、水銀ポロシメー
ターによる細孔分布測定において、全細孔容積が0.4
ml/g以上、細孔分布図から算出される平均細孔径が
20nm以上の特性を有してなるオイルミスト用吸着材
。1. A carbonaceous spherical body formed by adhering glassy carbon to the surface layer of carbon black pellets, which has a total pore volume of 0.4 in pore distribution measurement using a mercury porosimeter.
An adsorbent for oil mist having characteristics of ml/g or more and an average pore diameter calculated from a pore distribution diagram of 20 nm or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14347489A JPH038440A (en) | 1989-06-06 | 1989-06-06 | Adsorbent for oil mist |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14347489A JPH038440A (en) | 1989-06-06 | 1989-06-06 | Adsorbent for oil mist |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH038440A true JPH038440A (en) | 1991-01-16 |
Family
ID=15339540
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14347489A Pending JPH038440A (en) | 1989-06-06 | 1989-06-06 | Adsorbent for oil mist |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH038440A (en) |
-
1989
- 1989-06-06 JP JP14347489A patent/JPH038440A/en active Pending
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