CN1224034A - Method for preparing asphalt based spherical active carbon - Google Patents
Method for preparing asphalt based spherical active carbon Download PDFInfo
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- CN1224034A CN1224034A CN 98104975 CN98104975A CN1224034A CN 1224034 A CN1224034 A CN 1224034A CN 98104975 CN98104975 CN 98104975 CN 98104975 A CN98104975 A CN 98104975A CN 1224034 A CN1224034 A CN 1224034A
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- asphalt
- active carbon
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Abstract
A process for preparing spherical asphalt-base activated carbon includes mixing asphalt, organic metal compound and aromatic solvent in a ratio of 1 : (0.001-0.1) : (0.1-0.5) at 100-300 deg.C in a high-pressure tank, granulating by emulsification, non-melting treatment, charring, and activating. Obtained activated carbon features high total specific surface area up to 873-15171 sq.m/g, mesopores in different sizes with high specific surface area up to 153-475 sq.m/g, high activity and strength, low resistance, low cost and quick adsorption and desorption.
Description
The invention belongs to a kind of preparation method of gac, being specifically related to a kind of is the method for feedstock production spheric active carbon with pitch.
Characteristics such as the little and adsorption desorption speed of asphalt-base globular active carbon has good sphericity, physical strength height, fixed bed when using resistance is fast have obtained using widely in fields such as environmental protection, medical treatment, military affairs, chemical industry.But because the influence of the character of pitch own, the aperture of the asphalt-base globular active carbon that conventional steam activation makes belongs to range of micropores (＜20 ) mostly, can obtain the mesopore about a small amount of 20-40 after the deep activation, but can not obtain more wide-aperture mesopore.This has just limited the range of application of asphalt-base globular active carbon, particularly the application aspect the absorption of liquid phase macromole.Therefore press for and develop asphalt-base globular active carbon with flourishing central hole structure.
In order to improve the active of above-mentioned gac and to enlarge its range of application, people adopt the whole bag of tricks to increase its specific surface, particularly increase the ratio of mesopore (＞20 ) structure.For example, the An Tianyuan of Japan and Yu Jing such as take charge of for a long time at the macromolecule complex that the scholar utilizes organo-metallic mixture or metal, have prepared the gac [Chem.Mater.1996,8,454-462 and TANSO (Japanese) 1996,175,243-248] of mesopore prosperity.Used organo-metallic mixture and metal macromolecule complex need oneself preparation in its technology, and its preparation method mainly contains following three kinds:
(1) contains the self-polymerization of metal composite (as 2,4-hexadienyl [iron tricarbonyl] vinylformic acid) of vinyl or the copolymerization of these metal composites and vinyl cyanide (AN), vinylbenzene (ST), methyl methylacrylic acid (MMA) or 4-ethylpyridine (VP).
(2) metallic compound and the organic macromolecule that contains certain functional group (as poly-propionitrile (PAN), poly-ethylpyridine (PVP) and contain-COO-,-NR2 or cyclopentadienyl coordinate polystyrene (PST) etc.) form coordination compound.
(3) soluble metal organic macromolecule compound (as poly-ethyl dicyclopentadienyl iron, 1,1 ' two menaphthyl ferrocene etc.) mixes with pitch or organic polymer (as polyacrylonitrile (PAN), poly-ethylpyridine (PVP) etc.).
An Tianyuan and Yu Jing the scholar such as take charge of for a long time and adopt the third method more, mid-temperature pitch (SP=85 ℃) is dissolved in tetrahydrofuran (THF) or the quinoline, then with organometallic compound (as Y (acac)
3, Ln (C
5H
5)
3(Ln=Y, La, Yb, Nd, Sm, Gd etc.), (C
5H
5)
2CO, (C
5H
5)
2YbCl, Fe (C
5H
5)
2Deng) mix, under vacuum state, remove tetrahydrofuran (THF) or quinoline then, the pitch of the containing metal particulate that makes like this mixes with hard pitch (SP=280 ℃) again, after the fragmentation again through the gac that does not melt, charing, activation can make the mesopore prosperity.The BET and the aperture structure of the gac that above method makes are as shown in table 1.
Table 1
| Add metal | BET specific surface area (m 2/g) | Middle pore specific surface area (m 2/g) | Mesopore ratio (%) | Aperture () |
| Y(C 5H 5) 3 | ????210 | ????139 | ????66.3 | ????49.0 |
| Yb(C 5H 5) 3 | ????261 | ????193 | ????74.1 | ????56.8 |
| La(C 5H 5) 3 | ????191 | ????125 | ????65.5 | ????57.6 |
| YCl 3 | ????237 | ????40 | ????16.9 | ????33.8 |
The above results shows, although the mesopore ratio is higher, Zong because specific surface is few, the absolute value of mesopore specific surface is also little.Adopt organo-metallic mixture and the metal macromolecule complex that needs oneself to prepare in the technology, make the pitch of containing metal particulate with soft pitch after, also to increase and hard pitch blended step, not only make the preparation method complicated, also improved the cost of asphalt based active carbon greatly, it is unformed granular that the gained gac is, sphericity is poor, intensity difference in the use, resistance is big, and adsorption desorption speed is slow.
The objective of the invention is to develop the preparation method of a kind of total specific surface height, mesopore specific surface height, method asphalt-base globular active carbon simple, with low cost.
Preparation method of the present invention mixes general organometallic compound and hard pitch (SP=200-300 ℃) and aromatic solvent (one or more of benzene,toluene,xylene, naphthalene, methylnaphthalene), the homodisperse pitch of preparation metal particle, utilize the bitumen ball of the bitumen production containing metal particulate of containing metal particulate then, at last, with above-mentioned bitumen ball through do not melt, charing and activation treatment get the product gac.
The used asphalt stock of the present invention is that the useless pitch of the by product in petroleum pitch, coal-tar pitch, pitch earth or the oil refining makes it the hard pitch that modification obtains through thermal treatment or oxide treatment.
The used organometallic compound of the present invention is the organometallic compound (as ferrocene, nickelocene, three cyclopentadienyl yttriums, acetyl acetone yttrium etc.) of transition metal such as iron, nickel, yttrium or rare earth metal.
The detailed step of method is as follows:
1. containing metal particulate bituminous preparation
With pitch, organometallic compound and aromatic solvent with 1: (0.001-0.1): the high temperature (100-300 ℃) in autoclave of ratio (0.1-0.5) mixes, and can make and know the asphalt stock that is suitable for the containing metal particulate for preparing bitumen ball;
2. the asphalt emulsification balling-up that aforesaid method is made, the bitumen ball of preparation containing metal particulate;
3. the pre-treatment before the bitumen ball of containing metal particulate does not melt: add the bitumen ball that organometallic compound makes, utilize the method for vacuum extraction that aromatic solvent is removed, to make the porous asphalt ball of containing metal particulate.
4. the not melt processed of the bitumen ball of containing metal particulate: the porous asphalt ball of containing metal particulate is in oxidizing atmosphere, carry out not melt processed under 200-350 ℃ temperature, used oxidizing gas can be air or oxygen, ozone etc. and the gas mixture of rare gas element.
5. the charing of not melting the bitumen ball of containing metal particulate is handled: the bitumen ball that does not melt the containing metal particulate rises to 700-1200 ℃ with the temperature rise rate of 5-20 ℃/min and carries out charing and handle under protection of inert gas.
6. the activation treatment of the charing bitumen ball of containing metal particulate: the charing bitumen ball of containing metal particulate utilizes water vapor or carbonic acid gas to carry out activation treatment under 700-1200 ℃, can make the asphalt-base globular active carbon of mesopore prosperity.
Test-results is listed in table 2 and Fig. 1.
Fig. 1 is the pore size distribution of the asphalt based active carbon of interpolation ferrocene, and the Building X is designated as aperture (), and the Building Y is designated as pore volume (cm
3/ g)
Table 1
| Add metal | BET specific surface area (m 2/g) | Middle pore specific surface area (m 2/g) | Total pore volume (cm 3/g | Mesopore ratio * (%) | Mean pore size * * () |
| Ferrocene | ????1517 | ????475 | ????1.03 | ????63 | ????55 |
| Nickelocene | ????837 | ????153 | ????0.58 | ????41 | ????77 |
| The acetyl acetone yttrium | ????980 | ????190 | ????0.68 | ????43 | ????72 |
*: the mesopore ratio is drawn than total pore volume by mesopore volume;
*: mean pore size is drawn from desorption branch (4V/ ) by the BJH method.
The result shows:
1. total specific surface is up to 873-15171m2/ g, the mesopore specific surface is up to 153-475m2/ g wherein not only contains the mesopore of 20-40 , but also contains the mesopore of 300-500 , and average hole is 55-76 . Therefore, this active carbon is not only active high, and applied range.
2. increase the emulsion process balling-up of pitch in the method, gained active carbon sphericity is high, and intensity is high in therefore using, and resistance is little, and adsorption desorption is fast.
3. adopt common metallo-organic compound to make raw material, the substep that has simplified pitch adds, and has not only simplified operation, and has greatly reduced cost.
Embodiments of the invention are as follows:
Embodiment 1
Get 300 gram pitches, add 3 gram nickelocenes, 120 gram naphthalenes, in 140 ℃ of mixing and stirring, the cooling back is broken in autoclave, can be suitable for preparing the material asphalt of porous asphalt ball.With the pitch of above-mentioned containing metal particulate after the emulsion process balling-up, low temperature is removed naphthalene under vacuum state, be that oxidizing medium carries out not melt processed at 300 ℃ then with the air, again in nitrogen atmosphere in 900 ℃ of charings, then use water vapor 900 ℃ of activation, can make the asphalt-base globular active carbon of mesopore prosperity.
Get 300 gram pitches, add 12 gram acetyl acetone yttrium and 200 milliliters of benzene, in 120 ℃ of mixing and stirring, the cooling back is broken in autoclave, can be suitable for preparing the material asphalt of porous asphalt ball.Charing and activation temperature are 800 ℃, and other are with embodiment 1.
Embodiment 3
Get 300 gram pitches, add 6 gram ferrocene, 90 gram naphthalenes, in 170 ℃ of mixing and stirring, the cooling back is broken in autoclave, can be suitable for preparing the material asphalt of porous asphalt ball.Charing and activation temperature are 900 ℃, and other are with embodiment 1.
Claims (5)
1. the preparation method of an asphalt-base globular active carbon, it is by containing metal particulate bituminous preparation and this bituminous gives processings, melt processed, charing processing and activation treatment do not constitute, it is characterized in that described containing metal particulate bituminous preparation method be with common organometallic compound, aromatic solvent and hard pitch with 1: (0.001-0.1): the high temperature at 100-300 ℃ in autoclave of ratio (0.1-0.5) mixes.
2. the preparation method of asphalt-base globular active carbon as claimed in claim 1 is characterized in that having increased containing metal particulate bituminous emulsification balling-up and handles.
3. the preparation method of asphalt-base globular active carbon as claimed in claim 1 or 2 is characterized in that described organometallic compound is the organic compound of iron, nickel, yttrium transition metal or rare earth metal.
4. the preparation method of asphalt-base globular active carbon as claimed in claim 3 is characterized in that described organometallic compound is a ferrocene.
5. the preparation method of asphalt-base globular active carbon as claimed in claim 1 or 2 is characterized in that described aromatic solvent is naphthalene, methylnaphthalene, benzene,toluene,xylene.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN98104975A CN1089098C (en) | 1998-01-21 | 1998-01-21 | Method for preparing asphalt based spherical active carbon |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN98104975A CN1089098C (en) | 1998-01-21 | 1998-01-21 | Method for preparing asphalt based spherical active carbon |
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| CN1224034A true CN1224034A (en) | 1999-07-28 |
| CN1089098C CN1089098C (en) | 2002-08-14 |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100528747C (en) * | 2007-02-07 | 2009-08-19 | 中国科学院山西煤炭化学研究所 | Method for preparing medium pore carbon of narrow aperture and high degree of graphitization |
| CN104030287A (en) * | 2014-07-09 | 2014-09-10 | 四川创越炭材料有限公司 | Spherical activated carbon and preparation method thereof |
| CN105271225A (en) * | 2015-11-05 | 2016-01-27 | 新奥科技发展有限公司 | Preparing method for activated carbon |
| CN107572499A (en) * | 2017-10-16 | 2018-01-12 | 中国科学院山西煤炭化学研究所 | A kind of method and apparatus for preparing multi-functional Carbon Materials |
| CN109052397A (en) * | 2018-09-25 | 2018-12-21 | 湖南曦威新材料有限公司 | A kind of preparation method with hierarchical pore structure asphalt-base spherical activated carbon |
| CN111558363A (en) * | 2020-05-30 | 2020-08-21 | 深圳市儒碳新材料科技有限公司 | Asphalt-based one-shell multi-core magnetic carbon ball and preparation method thereof |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3917806A (en) * | 1973-09-27 | 1975-11-04 | Kureha Chemical Ind Co Ltd | Method for the preparation of carbon moldings and activated carbon molding therefrom |
| JPS6114110A (en) * | 1984-06-26 | 1986-01-22 | Kawasaki Steel Corp | Manufacture of fine and hollow body of carbon |
| CN1104075A (en) * | 1993-12-22 | 1995-06-28 | 刘以宁 | Special raincoat for motorcycle |
-
1998
- 1998-01-21 CN CN98104975A patent/CN1089098C/en not_active Expired - Fee Related
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100528747C (en) * | 2007-02-07 | 2009-08-19 | 中国科学院山西煤炭化学研究所 | Method for preparing medium pore carbon of narrow aperture and high degree of graphitization |
| CN104030287A (en) * | 2014-07-09 | 2014-09-10 | 四川创越炭材料有限公司 | Spherical activated carbon and preparation method thereof |
| CN104030287B (en) * | 2014-07-09 | 2015-11-18 | 四川创越炭材料有限公司 | A kind of spheric active carbon and preparation method thereof |
| CN105271225A (en) * | 2015-11-05 | 2016-01-27 | 新奥科技发展有限公司 | Preparing method for activated carbon |
| CN107572499A (en) * | 2017-10-16 | 2018-01-12 | 中国科学院山西煤炭化学研究所 | A kind of method and apparatus for preparing multi-functional Carbon Materials |
| CN109052397A (en) * | 2018-09-25 | 2018-12-21 | 湖南曦威新材料有限公司 | A kind of preparation method with hierarchical pore structure asphalt-base spherical activated carbon |
| CN109052397B (en) * | 2018-09-25 | 2021-12-03 | 湖南曦威新材料有限公司 | Preparation method of asphalt-based spherical activated carbon with hierarchical pore structure |
| CN111558363A (en) * | 2020-05-30 | 2020-08-21 | 深圳市儒碳新材料科技有限公司 | Asphalt-based one-shell multi-core magnetic carbon ball and preparation method thereof |
| CN111558363B (en) * | 2020-05-30 | 2021-03-23 | 中国石油大学(华东) | Asphalt-based one-shell multi-core magnetic carbon ball and preparation method thereof |
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| Publication number | Publication date |
|---|---|
| CN1089098C (en) | 2002-08-14 |
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