阅读说明：本技术 一种柱状载硫活性炭的制备方法 (Preparation method of columnar sulfur-carrying activated carbon ) 是由 许晓斌 陈辉 董文生 刘春玲 任满年 许金山 杨烨炜 高鹏 罗宵 于 2019-10-18 设计创作，主要内容包括：本发明属于活性炭的制备技术领域,具体涉及一种柱状载硫活性炭的制备方法。本发明以高硫石油焦为原料,用高硫渣油调制结合剂,结合剂与高硫石油焦共混成型后,经炭化和活化工艺处理,制备得到BET比表面积400～800m～2/g、载硫量5～13％、强度70～95％的柱状载硫活性炭。制备工艺简单,绿色环保；所用原料为炼油工艺副产品,对降低活性炭原料成本,提高重油加工的整体效益具有重要的意义。(The invention belongs to the technical field of preparation of activated carbon, and particularly relates to a preparation method of columnar sulfur-carrying activated carbon. The method takes high-sulfur petroleum coke as a raw material, uses high-sulfur residual oil to modulate a binding agent, and the high-sulfur petroleum coke and the binding agent are blended and molded and then are treated by carbonization and activation processes to prepare the high-sulfur petroleum coke with the BET specific surface area of 400-800 m 2 A columnar sulfur-carrying activated carbon with a sulfur-carrying amount of 5-13% and a strength of 70-95%. The preparation process is simple, green and environment-friendly; the raw material is a byproduct of the oil refining process, and has important significance for reducing the cost of the activated carbon raw material and improving the overall benefit of heavy oil processing.)

1. A preparation method of columnar sulfur-carrying activated carbon is characterized by comprising the following steps: the method comprises the following steps:

(1) binder formulation

Placing high-sulfur residual oil in a magnetic stirring reaction kettle, introducing air, nitrogen, oxygen or carbon dioxide at the flow rate of 1-30 mL/min, heating at the heating rate of 3-8 ℃/min until the high-sulfur residual oil in the reaction kettle is completely softened, starting a magnetic stirrer, carrying out constant-temperature reduced-pressure suction filtration for 30-200 min at the vacuum degree of 0-0.096 MPa and the temperature of 250-450 ℃, and discharging to obtain an asphalt binder with the softening point of 240-390 ℃;

the high-sulfur residual oil is high-sulfur atmospheric residual oil, high-sulfur vacuum residual oil or high-sulfur deoiled asphalt generated in the processing process of high-sulfur crude oil;

(2) shaping of

Respectively crushing the asphalt binder and the high-sulfur petroleum coke obtained in the step (1) to below 160 meshes, then loading the high-sulfur petroleum coke, the asphalt binder, water and the bonding aid into a kneading machine according to the mass ratio of 100: 20-100: 4-40: 2-30, uniformly kneading, extruding and molding at 10-50 ℃, standing at normal temperature for 36-60 hours, and obtaining a molded blank;

the bonding auxiliary agent is any one of polyvinyl alcohol, expanded starch, carboxymethyl cellulose, bone glue or diatomite;

(3) charring

Placing the formed blank obtained in the step (2) into a tubular resistance furnace, heating to 550-650 ℃ at a heating rate of 1-8 ℃/min under the protection of nitrogen, and keeping the temperature for 1-2 hours to obtain columnar carbon;

(4) activation of

And (3) under the protection of nitrogen, continuously heating the columnar carbon obtained in the step (3) to 750-950 ℃ under the condition of introducing water vapor with the flow rate of 0.3-0.8 mL/min, and carrying out activation treatment for 1-4 hours to obtain the columnar sulfur-carrying activated carbon.

2. The method for preparing the columnar sulfur-loaded activated carbon according to claim 1, characterized in that: in the step (1), the flow of the introduced air, nitrogen, oxygen or carbon dioxide is 7-20 mL/min.

3. The method for preparing the columnar sulfur-loaded activated carbon according to claim 2, characterized in that: in the step (1), air, nitrogen, oxygen or carbon dioxide is introduced at a flow rate of 12-15 mL/min.

4. The method for preparing the columnar sulfur-loaded activated carbon according to claim 1, characterized in that: in the step (1), the vacuum degree is-0.03 to-0.08 MPa, and the temperature is 300 to 400 ℃, and the constant temperature reduced pressure filtration is carried out for 70 to 150 min.

5. The method for preparing the columnar sulfur-loaded activated carbon according to claim 4, characterized in that: in the step (1), the vacuum filtration is carried out for 100-120 min at constant temperature and reduced pressure under the vacuum degree of-0.05-0.06 MPa and the temperature of 340-360 ℃.

6. The method for preparing the columnar sulfur-loaded activated carbon according to claim 1, characterized in that: in the step (2), the mass ratio of the high-sulfur petroleum coke to the asphalt binder, the water and the bonding auxiliary agent is 100: 40-80: 8-35: 8-25.

7. The method for preparing the columnar sulfur-loaded activated carbon according to claim 6, characterized in that: in the step (2), the mass ratio of the high-sulfur petroleum coke to the asphalt binder, the water and the bonding auxiliary agent is 100: 55-65: 20-25: 15-20.

8. The method for preparing the columnar sulfur-loaded activated carbon according to claim 1, characterized in that: and (2) extruding and molding at the temperature of 30-40 ℃.

9. The method for preparing the columnar sulfur-loaded activated carbon according to claim 1, characterized in that: in the step (4), under the protection of nitrogen, the columnar carbon obtained in the step (3) is continuously heated to 800-850 ℃ under the condition of introducing water vapor with the flow rate of 0.5mL/min, and is subjected to activation treatment for 2 hours.

Technical Field

The invention belongs to the technical field of preparation of activated carbon, and particularly relates to a preparation method of columnar sulfur-carrying activated carbon.

Background

Heavy metals have been difficult to control because of their strong toxicity, carcinogenicity, mutagenicity, difficult degradation and easy enrichment. Due to the combustion of fuel coal, the use of mercury-containing catalysts in petrochemical industry, etc., a large amount of mercury in different forms is emitted into the atmosphere. Mercury is an extremely toxic metal, and its compounds can cause irreversible neurological damage to the human body.

Activated carbon is a type of adsorbent with a developed pore structure and stable chemical properties, and although it has a high specific surface area, the mercury removal capacity of general activated carbon is generally weak due to high volatility of mercury and weak binding of mercury to the carbon surface. Research shows that sulfur-containing functional groups can be introduced to enhance the adsorption effect of the catalyst by adopting a surface sulfur-adding technology, especially for removing mercury. At present, sulfur-carrying activated carbon is generally prepared by chemically modifying ordinary activated carbon, for example, with sulfur, Na₂S or other sulfur-containing compounds are mixed with the activated carbon and then roasted to obtain the sulfur-loaded activated carbon, but the technology has the defects of toxic raw materials, high cost, complicated process and the like in the aspect of preparation process.

Along with the increase of the external dependence of crude oil in China, the processing of middle east imported high-sulfur crude oil is increased rapidly, and more high-sulfur petroleum cokes are generated. At present, high-sulfur petroleum coke is generally used as fuel in industries such as cement rotary kilns, glass melting furnaces and power plants. The new application of the high-sulfur petroleum coke is widened, the additional value of the low-value high-sulfur petroleum coke is improved, and the problem to be solved is needed.

Disclosure of Invention

The technical problem to be solved by the invention is as follows: the preparation method of the columnar sulfur-carrying activated carbon overcomes the defects of the prior art, adopts high-sulfur petroleum coke as a raw material, has simple preparation process, is green and environment-friendly, reduces the raw material cost of the activated carbon, and has important significance for improving the overall benefit of heavy oil processing.

The preparation method of the columnar sulfur-carrying activated carbon sequentially comprises the steps of preparing a binding agent, forming, carbonizing and activating.

The method specifically comprises the following steps:

(1) binder formulation

Placing high-sulfur residual oil in a magnetic stirring reaction kettle, introducing air, nitrogen, oxygen or carbon dioxide at the flow rate of 1-30 mL/min, heating at the heating rate of 3-8 ℃/min until the high-sulfur residual oil in the reaction kettle is completely softened, starting a magnetic stirrer, carrying out constant-temperature reduced-pressure suction filtration for 30-200 min at the vacuum degree of 0-0.096 MPa and the temperature of 250-450 ℃, and discharging to obtain an asphalt binder with the softening point of 240-390 ℃;

the high-sulfur residual oil is high-sulfur atmospheric residual oil, high-sulfur vacuum residual oil or high-sulfur deoiled asphalt generated in the processing process of high-sulfur crude oil;

(2) shaping of

Respectively crushing the asphalt binder and the high-sulfur petroleum coke obtained in the step (1) to below 160 meshes, then loading the high-sulfur petroleum coke, the asphalt binder, water and the bonding aid into a kneading machine according to the mass ratio of 100: 20-100: 4-40: 2-30, uniformly kneading, extruding and molding at 10-50 ℃, standing at normal temperature for 36-60 hours, and obtaining a molded blank;

the bonding auxiliary agent is any one of polyvinyl alcohol, expanded starch, carboxymethyl cellulose, bone glue or diatomite;

(3) charring

Placing the formed blank obtained in the step (2) into a tubular resistance furnace, heating to 550-650 ℃ at a heating rate of 1-8 ℃/min under the protection of nitrogen, and keeping the temperature for 1-2 hours to obtain columnar carbon;

(4) activation of

And (3) under the protection of nitrogen, continuously heating the columnar carbon obtained in the step (3) to 750-950 ℃ under the condition of introducing water vapor with the flow rate of 0.3-0.8 mL/min, and carrying out activation treatment for 1-4 hours to obtain the columnar sulfur-carrying activated carbon.

Wherein:

preferably, in the step (1), the flow of the introduced air, nitrogen, oxygen or carbon dioxide is 7-20 mL/min.

More preferably, in the step (1), the flow rate of the introduced air, nitrogen, oxygen or carbon dioxide is 12-15 mL/min.

Preferably, in the step (1), the vacuum filtration is carried out for 70-150 min at constant temperature and reduced pressure under the vacuum degree of-0.03 to-0.08 MPa and the temperature of 300-400 ℃.

More preferably, in the step (1), the vacuum filtration is carried out for 100-120 min at constant temperature and reduced pressure under the vacuum degree of-0.05-0.06 MPa and the temperature of 340-360 ℃.

Preferably, in the step (2), the mass ratio of the high-sulfur petroleum coke to the asphalt binder, the water and the bonding assistant is 100: 40-80: 8-35: 8-25.

More preferably, in the step (2), the mass ratio of the high-sulfur petroleum coke to the asphalt binder, the water and the bonding assistant is 100: 55-65: 20-25: 15-20.

Preferably, in the step (2), the extrusion molding is carried out at 30-40 ℃.

Preferably, in the step (4), under the protection of nitrogen, the columnar carbon obtained in the step (3) is continuously heated to 800-850 ℃ under the condition of introducing water vapor with the flow rate of 0.5mL/min, and is subjected to activation treatment for 2 hours.

The invention has the following beneficial effects:

1. the method takes high-sulfur petroleum coke as a raw material, uses high-sulfur residual oil to modulate a binding agent, and the high-sulfur petroleum coke and the binding agent are blended and molded and then are treated by carbonization and activation processes to prepare the high-sulfur petroleum coke with the BET specific surface area of 400-800 m²A columnar sulfur-carrying activated carbon with a sulfur-carrying amount of 5-13% and a strength of 70-95%.

2. Compared with the existing preparation method of the sulfur-carrying activated carbon, the preparation method is simple in process and environment-friendly. The raw material used by the method is a byproduct of an oil refining process, and has important significance for reducing the cost of the activated carbon raw material and improving the overall benefit of heavy oil processing.

3. The method of the invention uses high-sulfur petroleum coke as a raw material, and realizes high-value reutilization of the high-sulfur petroleum coke.

Detailed Description

The present invention is further illustrated by the following examples, which are not intended to limit the practice of the invention.

In the following examples, a fully automatic rapid specific surface area and porosity analyzer model ASAP-2020M, Michmark corporation, N₂The BET specific surface area of the activated carbon was measured at 77K. Before the measurement of the sample, the sample was treated at 250 ℃ for 8 hours (10-2Torr) under vacuum. The strength of the activated carbon is measured by using a GB/T7702.3-2008 coal granular activated carbon test method. The sulfur content is measured by an S2CLS-3000 type microcomputer coulomb sulfur detector.

Example 1

1. Binder formulation

And (2) loading 250g of high-sulfur vacuum residue into a magnetic stirring kettle, introducing air at the flow rate of 7mL/min, heating at the heating rate of 5 ℃/min until the high-sulfur vacuum residue in the reaction kettle is completely softened, starting the magnetic stirring kettle, adjusting the vacuum degree to-0.03 MPa when the temperature is increased to 300 ℃, carrying out constant-temperature vacuum filtration for 30min, and discharging to obtain the asphalt binder with the softening point of 243 ℃.

2. Shaping of

Respectively crushing the asphalt binder and the high-sulfur petroleum coke obtained in the step (1) to below 160 meshes, then loading the high-sulfur petroleum coke, the asphalt binder, the water and the bone glue into a kneading and extruding all-in-one machine according to the mass ratio of 100:40:10:20, uniformly kneading, extruding and molding at 30 ℃, and standing for 2 days at normal temperature to obtain a molded blank.

3. Charring

And (3) putting the formed blank obtained in the step (2) into a tubular resistance furnace, heating to 600 ℃ at the heating rate of 5 ℃/min under the protection of nitrogen, and keeping the temperature for 1 hour to obtain the columnar carbon.

4. Activation of

Under the protection of nitrogen, continuously heating the columnar carbon obtained in the step 3 to 800 ℃ under the condition of introducing water vapor with the flow rate of 0.5mL/min, and carrying out activation treatment for 2 hours to obtain the columnar sulfur-carrying activated carbon, wherein the BET specific surface area of the columnar sulfur-carrying activated carbon is 480m²Per g, sulfur loading 8 percent and strength 92 percent.

Example 2

1. Binder formulation

And (2) loading 250g of high-sulfur vacuum residue into a magnetic stirring kettle, introducing air at a flow rate of 7mL/min, heating at a heating rate of 5 ℃/min until the high-sulfur vacuum residue in the reaction kettle is completely softened, starting the magnetic stirring kettle, adjusting the vacuum degree to-0.06 MPa when the temperature is increased to 300 ℃, carrying out constant-temperature vacuum filtration for 90min, and discharging to obtain the asphalt binder with the softening point of 286 ℃.

2. Shaping of

Respectively crushing the asphalt binder and the high-sulfur petroleum coke obtained in the step (1) to below 160 meshes, then loading the high-sulfur petroleum coke, the asphalt binder, the water and the polyvinyl alcohol into a kneading and extruding all-in-one machine according to the mass ratio of 100:40:10:20, uniformly kneading, extruding and molding at 30 ℃, and standing for 2 days at normal temperature to obtain a molded blank.

3. Charring

And (3) putting the formed blank obtained in the step (2) into a tubular resistance furnace, heating to 600 ℃ at the heating rate of 5 ℃/min under the protection of nitrogen, and keeping the temperature for 1 hour to obtain the columnar carbon.

4. Activation of

Under the protection of nitrogen, continuously heating the columnar carbon obtained in the step 3 to 800 ℃ under the condition of introducing water vapor with the flow rate of 0.5mL/min, and carrying out activation treatment for 2 hours to obtain the columnar sulfur-carrying activated carbon, wherein the BET specific surface area of the columnar sulfur-carrying activated carbon is 532m²G, sulfur loading 10 percent and strength 93 percent.

Example 3

1. Binder formulation

And (2) loading 250g of high-sulfur vacuum residue into a magnetic stirring kettle, introducing air at a flow rate of 13mL/min, heating at a heating rate of 5 ℃/min until the high-sulfur vacuum residue in the reaction kettle is completely softened, starting the magnetic stirring kettle, adjusting the vacuum degree to-0.06 MPa when the temperature is increased to 300 ℃, carrying out constant-temperature vacuum filtration for 110min, and discharging to obtain the asphalt binder with the softening point of 346 ℃.

2. Shaping of

Respectively crushing the asphalt binder and the high-sulfur petroleum coke obtained in the step (1) to below 160 meshes, then loading the high-sulfur petroleum coke, the asphalt binder, the water and the expanded starch into a kneading and extruding all-in-one machine according to the mass ratio of 100:60:22:16, uniformly kneading, extruding and molding at 30 ℃, and standing at normal temperature for 2 days to obtain a molded blank.

3. Charring

And (3) putting the formed blank obtained in the step (2) into a tubular resistance furnace, heating to 600 ℃ at the heating rate of 5 ℃/min under the protection of nitrogen, and keeping the temperature for 1 hour to obtain the columnar carbon.

4. Activation of

Under the protection of nitrogen, the columnar carbon obtained in the step 3 is continuously heated to 850 ℃ under the condition of introducing water vapor with the flow rate of 0.5mL/min, and is subjected to activation treatment for 2 hours to obtain the columnar sulfur-loaded activated carbon, wherein the BET specific surface area of the columnar sulfur-loaded activated carbon is 764m²Per g, sulfur loading 6 percent and strength 90 percent.

Example 4

1. Binder formulation

And (2) loading 250g of high-sulfur vacuum residue into a magnetic stirring kettle, introducing air at a flow rate of 13mL/min, heating at a heating rate of 5 ℃/min until the high-sulfur vacuum residue in the reaction kettle is completely softened, starting the magnetic stirring kettle, adjusting the vacuum degree to-0.08 MPa when the temperature is increased to 300 ℃, carrying out constant-temperature vacuum filtration for 90min, and discharging to obtain the asphalt binder with the softening point of 358 ℃.

2. Shaping of

Respectively crushing the asphalt binder and the high-sulfur petroleum coke obtained in the step (1) to below 160 meshes, then loading the high-sulfur petroleum coke, the asphalt binder, the water and the diatomite into a kneading and extruding all-in-one machine according to the mass ratio of 100:40:10:20, uniformly kneading, extruding and molding at 30 ℃, and standing at normal temperature for 2 days to obtain a molded blank.

3. Charring

And (3) putting the formed blank obtained in the step (2) into a tubular resistance furnace, heating to 600 ℃ at the heating rate of 5 ℃/min under the protection of nitrogen, and keeping the temperature for 1 hour to obtain the columnar carbon.

4. Activation of

Under the protection of nitrogen, the columnar carbon obtained in the step 3 is continuously heated to 850 ℃ under the condition of introducing water vapor with the flow rate of 0.5mL/min, and is subjected to activation treatment for 2 hours to obtain the columnar sulfur-carrying activated carbon, wherein the BET specific surface area of the columnar sulfur-carrying activated carbon is 568m²/g、8% of sulfur-carrying agent and 92% of strength.

Example 5

1. Binder formulation

And (2) loading 250g of high-sulfur atmospheric residue into a magnetic stirring kettle, introducing air at the flow rate of 20mL/min, heating at the heating rate of 5 ℃/min until the high-sulfur atmospheric residue in the reaction kettle is completely softened, starting the magnetic stirring kettle, adjusting the vacuum degree to-0.08 MPa when the temperature is increased to 300 ℃, carrying out constant-temperature reduced-pressure suction filtration for 110min, and discharging to obtain the asphalt binder with the softening point of 388 ℃.

2. Shaping of

Respectively crushing the asphalt binder and the high-sulfur petroleum coke obtained in the step (1) to below 160 meshes, then loading the high-sulfur petroleum coke, the asphalt binder, the water and the bone glue into a kneading and extruding all-in-one machine according to the mass ratio of 100:80:35:25, uniformly kneading, extruding and molding at 30 ℃, and standing at normal temperature for 2 days to obtain a molded blank.

3. Charring

And (3) putting the formed blank obtained in the step (2) into a tubular resistance furnace, heating to 600 ℃ at the heating rate of 5 ℃/min under the protection of nitrogen, and keeping the temperature for 1 hour to obtain the columnar carbon.

4. Activation of

Under the protection of nitrogen, the columnar carbon obtained in the step 3 is continuously heated to 900 ℃ under the condition of introducing water vapor with the flow rate of 0.5mL/min, and is activated for 2 hours to obtain the columnar sulfur-carrying activated carbon, wherein the BET specific surface area of the columnar sulfur-carrying activated carbon is 511m²Per g, sulfur loading 5 percent and strength 84 percent.

Example 6

1. Binder formulation

And (2) loading 250g of high-sulfur atmospheric residue oil into a magnetic stirring kettle, introducing air at the flow rate of 20mL/min, heating at the heating rate of 5 ℃/min until the high-sulfur atmospheric residue oil in the reaction kettle is completely softened, starting the magnetic stirring kettle, adjusting the vacuum degree to be-0.08 MPa when the temperature is increased to 350 ℃, carrying out constant-temperature reduced-pressure suction filtration for 110min, and discharging to obtain the asphalt binder with the softening point of 388 ℃.

2. Shaping of

Respectively crushing the asphalt binder and the high-sulfur petroleum coke obtained in the step (1) to below 160 meshes, then loading the high-sulfur petroleum coke, the asphalt binder, the water and the bone glue into a kneading and extruding all-in-one machine according to the mass ratio of 100:40:10:20, uniformly kneading, extruding and molding at 30 ℃, and standing for 2 days at normal temperature to obtain a molded blank.

3. Charring

And (3) putting the formed blank obtained in the step (2) into a tubular resistance furnace, heating to 600 ℃ at the heating rate of 5 ℃/min under the protection of nitrogen, and keeping the temperature for 1 hour to obtain the columnar carbon.

4. Activation of

Under the protection of nitrogen, the columnar carbon obtained in the step 3 is continuously heated to 850 ℃ under the condition of introducing water vapor with the flow rate of 0.5mL/min, and is subjected to activation treatment for 2 hours to obtain the columnar sulfur-carrying activated carbon, wherein the BET specific surface area of the columnar sulfur-carrying activated carbon is 456m²G, sulfur carrying 7 percent and strength 95 percent.

Example 7

1. Binder formulation

And (2) loading 250g of high-sulfur vacuum residue into a magnetic stirring kettle, introducing air at the flow rate of 7mL/min, heating at the heating rate of 5 ℃/min until the high-sulfur vacuum residue in the reaction kettle is completely softened, starting the magnetic stirring kettle, adjusting the vacuum degree to-0.03 MPa when the temperature is increased to 350 ℃, carrying out constant-temperature vacuum filtration for 30min, and discharging to obtain the asphalt binder with the softening point of 243 ℃.

2. Shaping of

Respectively crushing the asphalt binder and the high-sulfur petroleum coke obtained in the step (1) to below 160 meshes, then loading the high-sulfur petroleum coke, the asphalt binder, the water and the bone glue into a kneading and extruding all-in-one machine according to the mass ratio of 100:40:10:20, uniformly kneading, extruding and molding at 40 ℃, and standing for 2 days at normal temperature to obtain a molded blank.

3. Charring

And (3) putting the formed blank obtained in the step (2) into a tubular resistance furnace, heating to 600 ℃ at the heating rate of 5 ℃/min under the protection of nitrogen, and keeping the temperature for 1 hour to obtain the columnar carbon.

4. Activation of

Under the protection of nitrogen, the columnar carbon obtained in the step 3 is continuously heated to 800 ℃ under the condition of introducing water vapor with the flow rate of 0.5mL/min, and is subjected to activation treatment for 2 hours to obtain the columnar carbonThe BET specific surface area of the sulfur-carrying activated carbon is 674m²Per g, 9 percent of sulfur and 94 percent of strength.

Example 8

1. Binder formulation

And (2) loading 250g of high-sulfur atmospheric residue into a magnetic stirring kettle, introducing air at the flow rate of 7mL/min, heating at the heating rate of 5 ℃/min until the high-sulfur atmospheric residue in the reaction kettle is completely softened, starting the magnetic stirring kettle, adjusting the vacuum degree to-0.06 MPa when the temperature is raised to 370 ℃, carrying out constant-temperature reduced-pressure suction filtration for 90min, and discharging to obtain the asphalt binder with the softening point of 286 ℃.

2. Shaping of

Respectively crushing the asphalt binder and the high-sulfur petroleum coke obtained in the step (1) to below 160 meshes, then loading the high-sulfur petroleum coke, the asphalt binder, the water and the bone glue into a kneading and extruding all-in-one machine according to the mass ratio of 100:40:10:20, uniformly kneading, extruding and molding at 20 ℃, and standing at normal temperature for 2 days to obtain a molded blank.

3. Charring

And (3) putting the formed blank obtained in the step (2) into a tubular resistance furnace, heating to 600 ℃ at the heating rate of 5 ℃/min under the protection of nitrogen, and keeping the temperature for 1 hour to obtain the columnar carbon.

4. Activation of

Under the protection of nitrogen, the columnar carbon obtained in the step 3 is continuously heated to 800 ℃ under the condition of introducing water vapor with the flow rate of 0.5mL/min, and is subjected to activation treatment for 2 hours to obtain the columnar sulfur-carrying activated carbon, wherein the BET specific surface area of the columnar sulfur-carrying activated carbon is 613m²G, sulfur loading 10 percent and strength 93 percent.

Example 9

1. Binder formulation

And (2) loading 250g of high-sulfur vacuum residue into a magnetic stirring kettle, introducing air at a flow rate of 13mL/min, heating at a heating rate of 5 ℃/min until the high-sulfur vacuum residue in the reaction kettle is completely softened, starting the magnetic stirring kettle, adjusting the vacuum degree to-0.06 MPa when the temperature is increased to 400 ℃, carrying out constant-temperature vacuum filtration for 110min, and discharging to obtain the asphalt binder with the softening point of 356 ℃.

2. Shaping of

Respectively crushing the asphalt binder and the high-sulfur petroleum coke obtained in the step (1) to below 160 meshes, then loading the high-sulfur petroleum coke, the asphalt binder, the water and the carboxymethyl cellulose into a kneading and extruding all-in-one machine according to the mass ratio of 100:60:22:16, uniformly kneading, extruding and molding at 20 ℃, and standing for 2 days at normal temperature to obtain a molded blank.

3. Charring

And (3) putting the formed blank obtained in the step (2) into a tubular resistance furnace, heating to 600 ℃ at the heating rate of 5 ℃/min under the protection of nitrogen, and keeping the temperature for 1 hour to obtain the columnar carbon.

4. Activation of

Under the protection of nitrogen, the columnar carbon obtained in the step 3 is continuously heated to 800 ℃ under the condition of introducing water vapor with the flow rate of 0.5mL/min, and is activated for 2 hours to obtain the columnar sulfur-carrying activated carbon, wherein the BET specific surface area of the columnar sulfur-carrying activated carbon is 800m²Per g, 13 percent of sulfur and 95 percent of strength.

Example 10

1. Binder formulation

And (2) loading 250g of high-sulfur deoiled asphalt into a magnetic stirring kettle, introducing air at the flow rate of 13mL/min, heating at the heating rate of 5 ℃/min until the high-sulfur deoiled asphalt in the reaction kettle is completely softened, starting the magnetic stirring kettle, adjusting the vacuum degree to-0.08 MPa when the temperature is increased to 350 ℃, carrying out constant-temperature reduced-pressure suction filtration for 90min, and discharging to obtain the asphalt binder with the softening point of 358 ℃.

2. Shaping of

Respectively crushing the asphalt binder and the high-sulfur petroleum coke obtained in the step (1) to below 160 meshes, then loading the high-sulfur petroleum coke, the asphalt binder, the water and the bone glue into a kneading and extruding all-in-one machine according to the mass ratio of 100:40:10:20, uniformly kneading, extruding and molding at 40 ℃, and standing for 2 days at normal temperature to obtain a molded blank.

3. Charring

And (3) putting the formed blank obtained in the step (2) into a tubular resistance furnace, heating to 600 ℃ at the heating rate of 5 ℃/min under the protection of nitrogen, and keeping the temperature for 1 hour to obtain the columnar carbon.

4. Activation of

Under the protection of nitrogen, the columnar carbon obtained in the step 3 is introduced at the flow rate of 0.5mL/miContinuously heating to 850 ℃ under the condition of n water vapor, and carrying out activation treatment for 2 hours to obtain columnar sulfur-carrying activated carbon with the BET specific surface area of 596m²G, sulfur loading of 7 percent and strength of 80 percent.

Example 11

1. Binder formulation

And (2) loading 250g of high-sulfur deoiled asphalt into a magnetic stirring kettle, introducing air at the flow rate of 20mL/min, heating at the heating rate of 5 ℃/min until the high-sulfur deoiled asphalt in the reaction kettle is completely softened, starting the magnetic stirring device, adjusting the vacuum degree to-0.08 MPa when the temperature is increased to 300 ℃, carrying out constant-temperature reduced-pressure suction filtration for 110min, and discharging to obtain the asphalt binder with the softening point of 362 ℃.

2. Shaping of

Respectively crushing the asphalt binder and the high-sulfur petroleum coke obtained in the step (1) to below 160 meshes, then loading the high-sulfur petroleum coke, the asphalt binder, the water and the expanded starch into a kneading and extruding all-in-one machine according to the mass ratio of 100:40:8:8, uniformly kneading, extruding and molding at 20 ℃, and standing at normal temperature for 2 days to obtain a molded blank.

3. Charring

And (3) putting the formed blank obtained in the step (2) into a tubular resistance furnace, heating to 600 ℃ at the heating rate of 5 ℃/min under the protection of nitrogen, and keeping the temperature for 1 hour to obtain the columnar carbon.

4. Activation of

Under the protection of nitrogen, the columnar carbon obtained in the step 3 is continuously heated to 900 ℃ under the condition of introducing water vapor with the flow rate of 0.5mL/min, and is activated for 2 hours to obtain the columnar sulfur-carrying activated carbon, wherein the BET specific surface area of the columnar sulfur-carrying activated carbon is 753m²Per g, 9 percent of sulfur and 70 percent of strength.