CN101816919A - Method for improving coke adsorption - Google Patents
Method for improving coke adsorption Download PDFInfo
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- CN101816919A CN101816919A CN 201010153112 CN201010153112A CN101816919A CN 101816919 A CN101816919 A CN 101816919A CN 201010153112 CN201010153112 CN 201010153112 CN 201010153112 A CN201010153112 A CN 201010153112A CN 101816919 A CN101816919 A CN 101816919A
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Abstract
The invention relates to a method for improving coke adsorption. The method comprises the following steps of: putting coke into a closed reactor; charging inert gas such as nitrogen or argon and the like into the closed reactor till the closed reactor has no air; when the inert gas such as nitrogen or argon and the like is charged, heating the closed reactor to between 800 and 1,100 DEG C; when the closed reactor is heated to 800 DEG C, introducing CO2 gas into the closed reactor till the pressure in the closed reactor reaches 1.1 to 2.0MPa, and stabilizing the pressure for 20 to 120 minutes; after the pressure stabilization is finished, stopping introducing the CO2 gas and heating; then introducing the inert gas such as nitrogen or argon and the like into the closed reactor till the closed reactor has no CO2 gas; meanwhile, naturally cooling the closed reactor to room temperature; and taking the modified coke out. The porosity of the modified coke is improved to 60 percent from primary 30 percent around; the vacuum degree is reduced to 800kg/m<3>, and reduced by nearly 30 percent compared with the un-modified coke; and inner micro-pores of the coke are obviously enlarged.
Description
Technical field
The present invention relates to coke, specifically belong to the method that improves or improve the coke adsorption energy.
Background technology
In the Environmental Technology field, coke is because of it has certain adsorptivity, cheapness, characteristics such as be easy to get, more and more adsorbents that are used as.But coke adsorption can low deep development and the application that is always restricting this adsorbent.Through actual measurement, the real density of coke is generally at 1100kg/m
3About, porosity is generally about 35%.Real density and porosity be influence coke adsorption can an important indicator, as in addition modification of STRENGTH ON COKE not, the absorption property of coke is then limited.Therefore improve the coke porosity, reduce the coke real density, improving coke adsorption can be to promote the key that coke is used in environmental project as adsorbent.The method that improves the coke adsorption energy at present is mainly crush method and chemical corrosion method: crush method is about to coke and is crushed to very little particle diameter, with raising coke ratio surface area, thus the absorption property of raising coke.Chemical corrosion method mainly is with strong acid or strong oxidizer chemicals corrosion coke surface, forms hole in coke surface, thereby improves the adsorptivity of coke.There is the shortcoming of following several respects in these two kinds of methods:
1) just improve the coke adsorption energy from improving the coke ratio surface area simply, and do not change the cavernous structure of coke inside, thus limited to the raising of absorption property.
2) coke after the crush method modification is a fine particle, and packing phenomenon in use takes place easily, causes and uses inconvenience.
3) chemical corrosion method easily causes spent acid and waste liquid in modifying process, forms secondary pollution.
3) crush method energy consumption in modifying process is higher, causes coke modification cost height.
Summary of the invention
The objective of the invention is to overcome above-mentioned deficiency, provide a kind of by improving charred coal porosity, reduce the coke real density and improve the inner cavernous structure of coke, thus improve coke adsorption can method.
Realize the technical measures of above-mentioned purpose:
A kind of method that improves coke adsorption, its step:
1) coke is inserted in the closed reactor of anti-1200 ℃ and above temperature;
2) inert gases such as nitrogen or argon gas are charged in the closed reactor, till no air exists in closed reactor; In inert gases such as inflated with nitrogen or argon gas, closed reactor is heated, the control heating-up temperature is 800~1100 ℃;
3) be heated when reaching 800 ℃ when closed reactor, begin to feed CO
2Gas, the pressure in closed reactor reaches 1.1~2.0Mpa, and voltage stabilizing 20~120 minutes under 1.1~2.0Mpa pressure, 800~1100 ℃ of temperature conditions;
4) after voltage stabilizing finishes, stop CO
2Gas input and heating;
5) stop CO
2Import inert gases such as nitrogen or argon gas immediately after the gas input, in closed reactor, do not have CO
2Till gas exists; Simultaneously, make closed reactor naturally cool to room temperature;
6) modified coke in the taking-up closed reactor.
It is: voltage stabilizing is 45~70 minutes under 1.1~2.0Mpa pressure, 800~1100 ℃ of temperature conditions.
The present invention is compared with prior art:
1) the coke porosity can bring up to 60% by original about 30% after its modification, compares with unmodified coke, and the porosity improves nearly one times;
2) real density can be reduced to 800kg/m
3, to compare with unmodified coke, real density reduces nearly 30%;
3) internal capillary of coke is also obviously increased.
Description of drawings
Fig. 1 is the internal capillary situation of the coke before the present invention
Fig. 2 is the internal capillary situation of coke behind employing the present invention
The specific embodiment
Be described in detail below
Embodiment 1
A kind of method that improves coke adsorption, its step:
1) coke is inserted in the closed reactor of anti-1200 ℃ and above temperature;
2) nitrogen is charged in the closed reactor, till no air exists in closed reactor; In inflated with nitrogen, closed reactor is heated to 800~830 ℃;
3) be heated when reaching 800 ℃ when closed reactor, begin to feed CO
2Gas, the pressure in closed reactor reaches 1.1Mpa, and voltage stabilizing 20 minutes under 1.1Mpa pressure, 800~830 ℃ of temperature conditions;
4) after voltage stabilizing finishes, stop CO
2Gas input and heating;
5) stop CO
2Import nitrogen immediately after the gas input, in closed reactor, do not have CO
2Till gas exists; Simultaneously, closed reactor is naturally cooled to room temperature;
6) modified coke in the taking-up closed reactor.
Embodiment 2
A kind of method that improves coke adsorption, its step:
1) coke is inserted in the closed reactor of anti-1200 ℃ and above temperature;
2) argon gas is charged in the closed reactor, till no air exists in closed reactor; In applying argon gas, closed reactor is heated to 890~910 ℃;
3) be heated when reaching 800 ℃ when closed reactor, begin to feed CO
2Gas, the pressure in closed reactor reaches 1.3Mpa, and voltage stabilizing 45 minutes under 1.3Mpa pressure, 890~910 ℃ of temperature conditions;
4) after voltage stabilizing finishes, stop CO
2Gas input and heating;
5) stop CO
2Import argon gas immediately after the gas input, in closed reactor, do not have CO
2Till gas exists; Simultaneously, closed reactor is naturally cooled to room temperature;
6) modified coke in the taking-up closed reactor.
Embodiment 3
A kind of method that improves coke adsorption, its step:
1) coke is inserted in the closed reactor of anti-1200 ℃ and above temperature;
2) nitrogen is charged in the closed reactor, till no air exists in closed reactor; In inflated with nitrogen, closed reactor is heated to 950~965 ℃;
3) be heated when reaching 800 ℃ when closed reactor, begin to feed CO
2Gas, the pressure in closed reactor reaches 1.55Mpa, and voltage stabilizing 70 minutes under 1.55Mpa pressure, 950~965 ℃ of temperature conditions;
4) after voltage stabilizing finishes, stop CO
2Gas input and heating;
5) stop CO
2Import nitrogen immediately after the gas input, in closed reactor, do not have CO
2Till gas exists; Simultaneously, closed reactor is naturally cooled to room temperature;
6) modified coke in the taking-up closed reactor.
Embodiment 4
A kind of method that improves coke adsorption, its step:
1) coke is inserted in the closed reactor of anti-1200 ℃ and above temperature;
2) nitrogen is charged in the closed reactor, till no air exists in closed reactor; In inflated with nitrogen, closed reactor is heated to 990~1015 ℃;
3) be heated when reaching 800 ℃ when closed reactor, begin to feed CO
2Gas, the pressure in closed reactor reaches 1.8Mpa, and voltage stabilizing 95 minutes under 1.8Mpa pressure, 990~1015 ℃ of temperature conditions;
4) after voltage stabilizing finishes, stop CO
2Gas input and heating;
5) stop CO
2Import nitrogen immediately after the gas input, in closed reactor, do not have CO
2Till gas exists; Simultaneously, closed reactor is naturally cooled to room temperature;
6) modified coke in the taking-up closed reactor.
Embodiment 5
A kind of method that improves coke adsorption, its step:
1) coke is inserted in the closed reactor of anti-1200 ℃ and above temperature;
2) nitrogen is charged in the closed reactor, till no air exists in closed reactor; In inflated with nitrogen, closed reactor is heated to 1085~1100 ℃;
3) be heated when reaching 800 ℃ when closed reactor, begin to feed CO
2Gas, the pressure in closed reactor reaches 2.0Mpa, and voltage stabilizing 120 minutes under 2.0Mpa pressure, 1085~1100 ℃ of temperature conditions;
4) after voltage stabilizing finishes, stop CO
2Gas input and heating;
5) stop CO
2Import nitrogen immediately after the gas input, in closed reactor, do not have CO
2Till gas exists; Simultaneously, closed reactor is naturally cooled to room temperature;
6) modified coke in the taking-up closed reactor.
Need to prove that in an embodiment, what charge in the closed reactor mostly is nitrogen greatly, is to consider the cost problem, because production costs such as neon, krypton gas, xenon are very high, so employing.When not considering cost, be to be used as the gas that charges into of the present invention fully.
The modified coke of the foregoing description after testing, it the results are shown in Table 1.
Table 1 modified coke testing result
Embodiment | ??1 | ??2 | ??3 | ??4 | ??5 |
Coke porosity (%) | ??39.12 | ??42.18 | ??48.37 | ??53.12 | ??57.64 |
Embodiment | ??1 | ??2 | ??3 | ??4 | ??5 |
Real density (kg/m 3) | ??951 | ??923 | ??882 | ??861 | ??823 |
Claims (2)
1. method that improves coke adsorption, its step:
1) coke is inserted in the closed reactor of anti-1200 ℃ and above temperature;
2) inert gases such as nitrogen or argon gas are charged in the closed reactor, till no air exists in closed reactor; In inert gases such as inflated with nitrogen or argon gas, closed reactor is heated, the control heating-up temperature is 800~1100 ℃;
3) be heated when reaching 800 ℃ when closed reactor, begin to feed CO
2Gas, the pressure in closed reactor reaches 1.1~2.0Mpa, and voltage stabilizing 20~120 minutes under 1.1~2.0Mpa pressure, 800~1100 ℃ of temperature conditions;
4) after voltage stabilizing finishes, stop CO
2Gas input and heating;
5) stop CO
2Import inert gases such as nitrogen or argon gas immediately after the gas input, in closed reactor, do not have CO
2Till gas exists; Simultaneously, make closed reactor naturally cool to room temperature;
6) modified coke in the taking-up closed reactor.
2. a kind of method that improves coke adsorption as claimed in claim 1 is characterized in that: voltage stabilizing is 45~70 minutes under 1.1~2.0Mpa pressure, 800~1100 ℃ of temperature conditions.
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CN 201010153112 CN101816919B (en) | 2010-04-16 | 2010-04-16 | Method for improving coke adsorption |
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CN 201010153112 CN101816919B (en) | 2010-04-16 | 2010-04-16 | Method for improving coke adsorption |
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CN101816919B CN101816919B (en) | 2013-01-23 |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103007883A (en) * | 2012-12-13 | 2013-04-03 | 武汉钢铁(集团)公司 | Iron and steel industrial wastewater iron remover and preparation method thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1031804A (en) * | 1988-10-22 | 1989-03-22 | 冶金工业部建筑研究总院 | Absorbent for greasy flue gas and preparation method thereof |
WO2006030668A1 (en) * | 2004-09-17 | 2006-03-23 | Nippon Petroleum Refining Company, Limited | Adsorbent, method for producing same, and method for processing oil-containing wastewater |
-
2010
- 2010-04-16 CN CN 201010153112 patent/CN101816919B/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1031804A (en) * | 1988-10-22 | 1989-03-22 | 冶金工业部建筑研究总院 | Absorbent for greasy flue gas and preparation method thereof |
WO2006030668A1 (en) * | 2004-09-17 | 2006-03-23 | Nippon Petroleum Refining Company, Limited | Adsorbent, method for producing same, and method for processing oil-containing wastewater |
Non-Patent Citations (1)
Title |
---|
《广西梧州师范高等专科学校学报》 20050930 谢复青,等 改性焦碳处理亚甲基蓝染料废水研究 第21卷, 第3期 2 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103007883A (en) * | 2012-12-13 | 2013-04-03 | 武汉钢铁(集团)公司 | Iron and steel industrial wastewater iron remover and preparation method thereof |
CN103007883B (en) * | 2012-12-13 | 2014-12-24 | 武汉钢铁(集团)公司 | Iron and steel industrial wastewater iron remover and preparation method thereof |
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