阅读说明：本技术 以氯化盐为模板剂制备电容炭并循环再生模板剂的方法 (Method for preparing capacitance carbon and circularly regenerating template by using chloride as template ) 是由 马新龙 杨子盼 李圣平 王成秀 高金森 于 2021-07-23 设计创作，主要内容包括：本发明提供了一种以氯化盐为模板剂制备电容炭并循环再生模板剂的方法,其包括(1)将超细的氯化盐粉末、碳的前驱体和活化剂按一定比例混合；(2)于惰性气氛中对步骤(1)所得混合物进行高温煅烧处理；(3)将步骤(2)所得反应产物酸洗至中性后烘干,得到所述电容炭；(4)对酸洗所得酸洗液进行蒸发结晶,得到再生的氯化盐,将再生的氯化盐循环至步骤(1)作为模板剂继续制备电容炭。本发明利用氯化盐作为模板剂制备电容炭材料,所用氯化盐模板剂可进行再生及循环使用,大大降低了电容炭材料的生产成本。同时,本发明制备得到的电容炭材料具有高比表面积和发达的孔道结构,且具有优异的电容特性,在电容器中具有良好的应用前景。(The invention provides a method for preparing capacitance carbon and circularly regenerating a template by taking chloride as the template, which comprises the following steps of (1) mixing superfine chloride powder, a precursor of carbon and an activating agent according to a certain proportion; (2) carrying out high-temperature calcination treatment on the mixture obtained in the step (1) in an inert atmosphere; (3) pickling the reaction product obtained in the step (2) to be neutral, and drying to obtain the capacitance carbon; (4) and (3) evaporating and crystallizing the pickling solution obtained by pickling to obtain regenerated chloride, and circulating the regenerated chloride to the step (1) to be used as a template agent to continuously prepare the capacitance carbon. According to the invention, the chloride is used as the template agent to prepare the capacitance carbon material, and the chloride template agent can be regenerated and recycled, so that the production cost of the capacitance carbon material is greatly reduced. Meanwhile, the capacitance carbon material prepared by the invention has high specific surface area, developed pore structure, excellent capacitance characteristic and good application prospect in capacitors.)

1. A method for preparing capacitance carbon by taking chloride as a template and recycling the template is characterized by comprising the following steps:

(1) mixing superfine chloride powder, a precursor of carbon and an activating agent according to a certain proportion;

(2) carrying out high-temperature calcination treatment on the mixture obtained in the step (1) in an inert atmosphere;

(3) pickling the reaction product obtained in the step (2) to be neutral, and drying to obtain the capacitance carbon;

(4) and (3) evaporating and crystallizing the pickling solution obtained by pickling to obtain regenerated chloride, and circulating the regenerated chloride to the step (1) to be used as a template agent to continuously prepare the capacitance carbon.

2. The method according to claim 1, wherein the mass ratio of the chloride salt powder, the carbon precursor and the activator is 0.5:1:1 to 10:1: 1.

3. The method according to claim 1 or 2, characterized in that the chloride salt powder has a particle size in the numerical range of 2-15 μ ι η;

preferably, the chloride salt powder comprises sodium chloride and/or potassium chloride.

4. The method of claim 1 or 2, wherein the carbon precursor comprises one or more of petroleum pitch, coal pitch, waste tire pyrolysis oil, vacuum residuum, wax oil, and petroleum coke.

5. A method according to claim 1 or 2, characterized in that the activator comprises potassium hydroxide and/or sodium hydroxide.

6. The method of claim 1 or 2, wherein the inert atmosphere comprises one or a combination of nitrogen, argon and helium.

7. The method as claimed in claim 1 or 2, wherein the calcination temperature is 600-1200 ℃ and the time is 0.5-5 h;

preferably, the temperature of the calcination is 700-900 ℃ and the time is 1-2 h.

8. The capacitance carbon material prepared by the method for preparing capacitance carbon by taking chloride as a template agent and circularly regenerating the template agent as claimed in any one of claims 1 to 7;

preferably, the pore size distribution of the capacitance carbon material is 1-100nm, and the specific surface area range is 1000-2000m²/g。

9. Use of the capacitive carbon material of claim 8 in a supercapacitor.

10. A super capacitor, wherein the electrode material is the capacitance carbon material as claimed in claim 8.

Technical Field

The invention relates to a method for preparing capacitance carbon by taking chloride as a template agent and circularly regenerating the template agent, belonging to the technical field of functional carbon materials.

Background

The capacitance carbon material is a carbon material with a high specific surface area and a highly developed pore structure, the pore size distribution of the carbon material can be regulated according to actual requirements, and the pore size can be between a nanometer level and a micron level. The capacitance carbon material has the advantages of high chemical stability, low price, narrow pore size distribution, good conductivity and the like, wherein the pore size range of the capacitance carbon material can be divided into three categories: micropores (<2nm), mesopores (2-50nm) and macropores (>50nm), and the existence of the pore structure helps to enhance the adsorption capacity and increase the specific surface area of the carbon material. Therefore, the capacitance carbon material can be applied to the capacitance storage field.

The conventional methods for preparing the capacitance carbon material mainly comprise an activation method and a template method, wherein the activation method comprises methods of chemical activation, physical activation, carbonization and activation of biomass, carbonization and activation of high molecular polymer and the like. Disordered capacitance carbon is usually synthesized by using the traditional activation methods, and the shape and the size of the pore channel of the disordered capacitance carbon are not easy to control. The template method is a method for copying the morphology and the pore structure of a template agent into a carbon material by selecting a proper template agent. The template method mainly includes a soft template method, a hard template method and a double template method. The hard template method is characterized in that a material with a unique pore structure and a special shape is selected as a template, a precursor of carbon is introduced into a pore channel of the template, the precursor of the carbon is subjected to a carbonization reaction under a high-temperature condition, and finally the template is removed to obtain the capacitance carbon with the shape similar to that of the template. The double-template method is to control the shape and pore channels of carbon material with hard template and soft template separately to obtain capacitance carbon with multilevel pore channels. The most remarkable advantage of the template method is that the synthesized capacitance carbon material has good structural stability and structural controllability, and can realize the mass production of the capacitance carbon material. Johnson et al (Chemistry of Materials 1997; 9(11):2448-58.) select phenolic resin as precursor of carbon, respectively adopt Y-type, L-type and Beta-type molecular sieves as template agent, successfully prepare microporous carbon by template method, the synthetic method has low operation cost, and is easy to realize the mass preparation of microporous carbon. Fang et al (Journal of Materials Chemistry 2010; 20(45):10253-9.) prepared an ordered multi-channel mesoporous carbon material having a large specific surface area and pore volume using a composite of monodisperse PS microspheres and nano silicon particles as a template and furfuryl alcohol as a precursor of carbon by a templating method.

In the current research process, after the template is removed by acid washing, the removed template cannot be recycled, so that the waste of the template agent is caused, and the production cost is increased. Therefore, the cyclic regeneration of the template agent in the preparation of the capacitance carbon material by using the template method has become a technical problem which needs to be solved in the field.

Disclosure of Invention

In order to solve the above disadvantages and shortcomings, an object of the present invention is to provide a method for preparing capacitance carbon using chloride as a template and recycling the template.

The invention also aims to provide a capacitance carbon material prepared by the method.

It is also an object of the present invention to provide the use of the above-described capacitive carbon material in a supercapacitor.

The invention also aims to provide a super capacitor, wherein the electrode material of the super capacitor is the capacitance carbon material.

In order to achieve the above objects, in one aspect, the present invention provides a method for preparing capacitance carbon using chloride salt as a template and recycling the template, wherein the method comprises:

(1) mixing superfine chloride powder, a precursor of carbon and an activating agent according to a certain proportion;

(2) carrying out high-temperature calcination treatment on the mixture obtained in the step (1) in an inert atmosphere;

(3) pickling the reaction product obtained in the step (2) to be neutral, and drying to obtain the capacitance carbon;

(4) and (3) evaporating and crystallizing the pickling solution obtained by pickling to obtain regenerated chloride, and circulating the regenerated chloride to the step (1) to be used as a template agent to continuously prepare the capacitance carbon.

In one embodiment of the above method of the present invention, the mass ratio of the chloride powder, the carbon precursor and the activator is 0.5:1:1 to 10:1: 1.

In one embodiment of the above method of the present invention, the particle size of the chloride powder is in the range of 2 to 15 μm.

In one embodiment of the above method of the present invention, the chloride salt powder comprises sodium chloride and/or potassium chloride.

According to the invention, the capacitor carbon is prepared by taking chloride as a template agent, wherein the chloride is low in price and easy to dissolve; in one embodiment of the present invention, commercial chloride salt may be first pulverized and then the larger particles of chloride salt are prepared into ultrafine chloride salt powder.

As a specific embodiment of the above method of the present invention, the carbon precursor includes one or more of petroleum pitch, coal pitch, waste tire cracking oil (waste tire oil), vacuum residue, wax oil and petroleum coke.

In a specific embodiment of the above method of the present invention, the activating agent comprises potassium hydroxide and/or sodium hydroxide.

As a specific embodiment of the above method of the present invention, the inert atmosphere includes one or a combination of nitrogen, argon and helium.

As a specific embodiment of the above method of the present invention, wherein the temperature of the calcination is 600-1200 ℃, and the time is 0.5-5 h;

preferably, the temperature of the calcination is 700-900 ℃ and the time is 1-2 h.

In the above-described method step (2) of the present invention, the precursor of carbon is activated and carbonized during the high-temperature calcination treatment.

In the step (3) of the method, the reaction product obtained in the step (2) is cooled to room temperature, and then is washed with acid to be neutral and dried. The temperature and time for drying are not specifically required, and the skilled in the art can reasonably set according to the actual operation needs on site as long as the reaction product can be dried. For example, in one embodiment of the present invention, the drying temperature is 100 ℃.

In the step (3) of the method of the present invention, the acid solution used for pickling is dilute hydrochloric acid, and the present invention does not specifically require the concentration of the dilute hydrochloric acid, and those skilled in the art can reasonably set the concentration of the dilute hydrochloric acid according to the actual operation needs on site, as long as the purposes of pickling, chloride regeneration and cyclic utilization of the present invention can be achieved.

In the step (4) of the method, the pickling solution obtained after pickling is evaporated, concentrated, crystallized and dried to obtain regenerated chloride, and the regenerated chloride can be recycled to the step (1) to be used as a template agent to continuously prepare the capacitor carbon, so that the regeneration and recycling of the chloride template agent are realized, and the batch production of the capacitor carbon material is ensured by the regeneration and recycling of the chloride template agent.

The temperature and time for drying in the step (4) are not specifically required, and the technical personnel in the field can reasonably set according to the actual operation needs on site as long as the regenerated chloride salt can be dried.

On the other hand, the invention also provides the capacitance carbon material prepared by the method for preparing the capacitance carbon by taking the chloride as the template and circularly regenerating the template.

As a specific embodiment of the above capacitance carbon material of the present invention, the pore size distribution of the capacitance carbon material is 1-100nm, and the specific surface area range is 1000-2000m²/g。

In another aspect, the invention also provides the application of the capacitance carbon material in the super capacitor.

In another aspect, the invention further provides a super capacitor, wherein the electrode material of the super capacitor is the capacitance carbon material.

The capacitance carbon material prepared by the invention has high specific surface area and developed pore structure, and when the capacitance carbon material is used as an electrode material of a super capacitor, the capacitance carbon material shows excellent capacitance storage characteristics.

According to the invention, heavy components such as chloride, petroleum asphalt, coal asphalt, waste tire pyrolysis oil, vacuum residuum, wax oil and petroleum coke are respectively adopted as a template agent and a carbon source for the growth of capacitance carbon, a mixture of the heavy components, the chloride and an activating agent is subjected to high-temperature calcination treatment in an inert atmosphere based on a directional guide coupling in-situ activation technology, and a high-performance capacitance carbon material with a high specific surface area and a developed pore structure is prepared under the guide of the template agent and the activation of the activating agent; in the process of pickling and purifying the capacitance carbon material, the obtained pickling solution is a chloride solution, and after evaporation and crystallization, chloride crystals can be obtained again, so that the regeneration and the full cyclic utilization of the chloride template agent are realized; meanwhile, the method provided by the invention is green and environment-friendly, the operation condition is easy to control, and the operation cost is low.

In conclusion, the invention uses the chloride as the template agent, and the chloride can be regenerated and recycled, thereby greatly reducing the production cost of the capacitance carbon material. Meanwhile, the capacitance carbon material prepared by the invention has high specific surface area, developed pore structure, excellent capacitance characteristic and good application prospect in capacitors.

Drawings

In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings needed to be used in the description of the embodiments will be briefly introduced below, and it is obvious that the drawings in the following description are some embodiments of the present invention, and it is obvious for those skilled in the art that other drawings can be obtained according to these drawings without creative efforts.

Fig. 1 is a scanning electron microscope image of the capacitance carbon material prepared in step (3) of example 1 of the present invention.

FIG. 2 is a scanning electron microscope image of a capacitance carbon material obtained when the regenerated potassium chloride is recycled to step (1) as a template in step (4) of example 1 of the present invention to continue to prepare the capacitance carbon material.

Fig. 3 is a nitrogen adsorption and desorption curve of the capacitance carbon material prepared in step (3) of example 1 of the present invention.

Fig. 4 is a pore distribution curve of the capacitance carbon material prepared in step (3) of example 1 of the present invention.

Fig. 5 is a nitrogen adsorption and desorption curve of the capacitance carbon material prepared in step (3) of example 2 of the present invention.

Fig. 6 is a pore distribution curve of the capacitance carbon material prepared in step (3) of example 2 of the present invention.

FIG. 7 is a scanning electron microscope image of a capacitance carbon material obtained by recycling the regenerated potassium chloride in step (4) of example 2 to step (1) as a template to continue the preparation of the capacitance carbon material.

Fig. 8 is a pore distribution curve of the capacitance carbon material prepared in step (3) of example 3 of the present invention.

Fig. 9 is a nitrogen adsorption and desorption curve of the capacitance carbon material prepared in step (3) of example 4 of the present invention.

FIG. 10 is a scanning electron micrograph of an initial sodium chloride templating agent in step (1) of example 4 of the present invention.

FIG. 11 is a scanning electron micrograph of a sodium chloride template after recycling in step (4) of example 4 of the present invention.

Fig. 12 is a nitrogen adsorption/desorption curve of the capacitance carbon material obtained in step (3) of example 5 of the present invention.

FIG. 13 is a pore distribution curve of the carbon material for capacitors obtained in step (3) of example 5 of the present invention.

Fig. 14 is a nitrogen adsorption/desorption curve of the capacitance carbon material obtained in step (3) of example 6 of the present invention.

FIG. 15 is a pore distribution curve of a capacitance carbon material obtained in step (3) of example 6 of the present invention.

Fig. 16 is a nitrogen adsorption/desorption curve of the capacitance carbon material obtained in step (3) of example 7 of the present invention.

FIG. 17 is a pore distribution curve of a capacitance carbon material obtained in step (3) of example 7 of the present invention.

Fig. 18 is a cyclic voltammogram of the capacitive carbon material obtained in step (3) of example 5 as an electrode material of a supercapacitor in examples 5 to 5 of the present invention at different scanning speeds.

Fig. 19 is a constant current charge and discharge curve of the capacitive carbon material prepared in step (3) of example 6 as an electrode material of a supercapacitor in examples 6 to 6 of the present invention.

Fig. 20 is a rate performance curve of the capacitive carbon material obtained in step (3) of example 7 as an electrode material of a supercapacitor in examples 7 to 7 of the present invention.

Detailed Description

In order to clearly understand the technical features, objects and advantages of the present invention, the following detailed description of the technical solutions of the present invention will be made with reference to the following specific examples, which should not be construed as limiting the implementable scope of the present invention.

Example 1

The embodiment provides a method for preparing capacitance carbon by using chloride as a template and recycling the template, wherein the method comprises the following steps:

(1) weighing 20g of potassium chloride, 10g of petroleum asphalt and 10g of potassium hydroxide, and fully and uniformly mixing;

(2) placing the mixture in a porcelain boat, placing the porcelain boat in a horizontal tube furnace, introducing Ar into the horizontal tube furnace, simultaneously raising the temperature of the horizontal tube furnace to 700 ℃ at a heating rate of 10 ℃/min, and keeping the temperature for 60min to calcine the mixture;

(3) after the furnace temperature is naturally cooled to room temperature, taking out a black product, placing the black product in a dilute hydrochloric acid solution, carrying out reflux acid washing for 1h to remove a potassium chloride template agent, drying the obtained product at 100 ℃, and obtaining the capacitance carbon material after the drying is finished; the dilute hydrochloric acid solution is prepared by firstly calculating the using amount of concentrated hydrochloric acid (the mass concentration is 36% -38%) with the required standard concentration according to the amount of potassium hydroxide used in the embodiment 1 and then preparing the concentrated hydrochloric acid with the standard concentration and distilled water according to the volume ratio of 1: 3;

(4) and (3) evaporating and crystallizing the pickling solution obtained by pickling, drying the obtained crystal to obtain regenerated potassium chloride, and circulating the regenerated potassium chloride to the step (1) to be used as a template agent to continuously prepare the capacitance carbon material.

Scanning electron microscope analysis is performed on the capacitance carbon material prepared in the step (3) of this embodiment to obtain a scanning electron microscope image of the capacitance carbon material, the scanning electron microscope image is shown in fig. 1, and it can be seen from fig. 1 that the capacitance carbon material prepared in the step (3) has a relatively rich pore structure.

The nitrogen adsorption-desorption curve and the pore distribution curve of the capacitance carbon material prepared in the step (3) of the embodiment are respectively shown in fig. 3 and fig. 4, and the specific surface area of the capacitance carbon material is 1109m²The pore diameter is mainly distributed between 2 and 30 nm; from the above results, it can be seen that the capacitance carbon material prepared in this embodiment has a high specific surface area and a developed pore structure.

Scanning electron microscope analysis is performed on the capacitance carbon material prepared when the regenerated potassium chloride in the step (4) of the embodiment is recycled to the step (1) and used as a template to continuously prepare the capacitance carbon material, an obtained scanning electron microscope image is shown in fig. 2, and as can be seen by comparing fig. 1 and fig. 2, the capacitance carbon materials prepared in the steps (3) and (4) of the embodiment both have rich pore channel structures, which indicates that the regenerated potassium chloride can be repeatedly used as the template to continuously prepare the capacitance carbon material.

Example 2

The embodiment provides a method for preparing capacitance carbon by using chloride as a template and recycling the template, wherein the method comprises the following steps:

(1) weighing 40g of potassium chloride, 10g of petroleum asphalt and 10g of potassium hydroxide, and fully and uniformly mixing;

(2) placing the mixture in a porcelain boat, placing the porcelain boat in a horizontal tube furnace, introducing Ar into the furnace, simultaneously raising the temperature of the horizontal tube furnace to 700 ℃ at a temperature rise rate of 10 ℃/min, and keeping the temperature for 60min to calcine the mixture;

(3) naturally cooling the furnace temperature of the horizontal tube furnace to room temperature, taking out a black product, placing the black product in a dilute hydrochloric acid solution, carrying out reflux acid washing for 1h to remove a potassium chloride template agent, drying the obtained product at 100 ℃, and obtaining the capacitance carbon material after the drying is finished; the dilute hydrochloric acid solution is prepared by firstly calculating the dosage of concentrated hydrochloric acid (the mass concentration is 36% -38%) with the required standard concentration according to the amount of potassium hydroxide used in the embodiment 2, and then mixing the concentrated hydrochloric acid with the standard concentration and distilled water according to the ratio of 1: 3;

(4) and (3) evaporating and crystallizing the pickling solution obtained by pickling, drying the obtained crystal to obtain regenerated potassium chloride, and circulating the regenerated potassium chloride to the step (1) to be used as a template agent to continuously prepare the capacitance carbon material.

The nitrogen adsorption-desorption curve and the pore distribution curve of the capacitance carbon material prepared in the step (3) of the present embodiment are shown in fig. 5 and 6, respectively, and it can be seen from fig. 5 and 6 that the specific surface area of the capacitance carbon material is 1365m²(ii)/g, pore size distribution of 2-100 nm.

Scanning electron microscope analysis is performed on the capacitance carbon material prepared when the regenerated potassium chloride in the step (4) of the embodiment is recycled to the step (1) and used as a template to continuously prepare the capacitance carbon material, an obtained scanning electron microscope image is shown in fig. 7, and as can be seen from fig. 7, the capacitance carbon material still has a relatively rich pore structure, which indicates that the regenerated potassium chloride can be repeatedly used as the template to continuously prepare the capacitance carbon material.

Example 3

The embodiment provides a method for preparing capacitance carbon by using chloride as a template and recycling the template, wherein the method comprises the following steps:

(1) weighing 20g of potassium chloride, 10g of waste tire pyrolysis oil and 10g of potassium hydroxide, and fully and uniformly mixing;

(2) placing the mixture in a porcelain boat, placing the porcelain boat in a horizontal tube furnace, introducing Ar into the furnace, simultaneously raising the temperature of the horizontal tube furnace to 750 ℃ at a temperature rise rate of 10 ℃/min, and keeping the temperature for 60min so as to calcine the mixture;

(3) naturally cooling the furnace temperature of the horizontal tube furnace to room temperature, taking out a black product, placing the black product in a dilute hydrochloric acid solution, carrying out reflux acid washing for 1h to remove a potassium chloride template agent, drying the obtained product at 100 ℃, and obtaining the capacitance carbon material after the drying is finished; the dilute hydrochloric acid solution is prepared by firstly calculating the dosage of concentrated hydrochloric acid (the mass concentration is 36% -38%) with the required standard concentration according to the amount of potassium hydroxide used in the embodiment 3 and then mixing the concentrated hydrochloric acid with the standard concentration and distilled water according to the ratio of 1: 3;

(4) and (3) evaporating and crystallizing the pickling solution obtained by pickling, drying the obtained crystal to obtain regenerated potassium chloride, and circulating the regenerated potassium chloride to the step (1) to be used as a template agent to continuously prepare the capacitance carbon material.

The specific surface area of the capacitance carbon material prepared in the step (3) of the embodiment is 1805m²The pore distribution curve is shown in figure 8, and as can be seen from figure 8, the pore size distribution of the capacitance carbon material is 2-40 nm.

Example 4

The embodiment provides a method for preparing capacitance carbon by using chloride as a template and recycling the template, wherein the method comprises the following steps:

(1) weighing 10g of sodium chloride, 10g of vacuum residue and 10g of sodium hydroxide, and fully and uniformly mixing;

(2) placing the mixture in a porcelain boat, placing the porcelain boat in a horizontal tube furnace, introducing Ar into the furnace, simultaneously raising the temperature of the horizontal tube furnace to 700 ℃ at a temperature rise rate of 10 ℃/min, and keeping the temperature for 60min to calcine the mixture;

(3) naturally cooling the furnace temperature of the horizontal tube furnace to room temperature, taking out a black product, placing the black product in a dilute hydrochloric acid solution, carrying out reflux acid washing for 1h to remove a sodium chloride template agent, drying the obtained product at 100 ℃, and obtaining the capacitance carbon material after the drying is finished; the dilute hydrochloric acid solution is prepared by firstly calculating the dosage of concentrated hydrochloric acid (the mass concentration is 36% -38%) with the required standard concentration according to the amount of sodium hydroxide used in the embodiment 4 and then mixing the concentrated hydrochloric acid with the standard concentration and distilled water according to the ratio of 1: 3;

(4) and (3) evaporating and crystallizing the pickling solution obtained by pickling, drying the obtained crystal to obtain regenerated sodium chloride, and circulating the regenerated sodium chloride to the step (1) to be used as a template agent to continuously prepare the capacitance carbon material.

The nitrogen adsorption and desorption curve of the capacitance carbon material prepared in the step (3) of the embodiment is shown in fig. 9, and as can be seen from fig. 9, the specific surface area is 1570m²(ii)/g; the pore size distribution of the capacitance carbon material is 2-50 nm.

In this embodiment, the scanning electron microscope image of the initial sodium chloride template and the scanning electron microscope image of the sodium chloride template after the recycling in step (4) are respectively shown in fig. 10 and fig. 11, and as can be seen from fig. 10 and fig. 11, the morphology of the initial sodium chloride template is substantially the same as the morphology of the sodium chloride template after the recycling in step (4), which indicates that in this embodiment, the sodium chloride template can be obtained by recycling and recycled to step (1) as the template to continue to prepare the capacitive carbon material, and since the morphology of the initial sodium chloride template is substantially the same as the morphology of the sodium chloride template after the recycling in step (4), the performance of the capacitive carbon material prepared in step (3) and step (4) is also substantially the same.

Example 5

The embodiment provides a method for preparing capacitance carbon by using chloride as a template and recycling the template, wherein the method comprises the following steps:

(1) weighing 30g of potassium chloride, 10g of coal tar pitch and 10g of potassium hydroxide, and fully and uniformly mixing;

(2) placing the mixture in a porcelain boat, placing the porcelain boat in a horizontal tube furnace, introducing Ar into the furnace, simultaneously raising the temperature of the horizontal tube furnace to 750 ℃ at a temperature rise rate of 10 ℃/min, and keeping the temperature for 60min so as to calcine the mixture;

(3) naturally cooling the furnace temperature of the horizontal tube furnace to room temperature, taking out a black product, placing the black product in a dilute hydrochloric acid solution, carrying out reflux acid washing for 1h to remove a potassium chloride template agent, drying the obtained product at 100 ℃, and obtaining the capacitance carbon material after the drying is finished; the dilute hydrochloric acid solution is prepared by firstly calculating the using amount of concentrated hydrochloric acid (the mass concentration is 36% -38%) with the required standard concentration according to the amount of potassium hydroxide used in the embodiment 5 and then mixing the concentrated hydrochloric acid with the standard concentration and distilled water according to the ratio of 1: 3;

(4) and (3) evaporating and crystallizing the pickling solution obtained by pickling, drying the obtained crystal to obtain regenerated potassium chloride, and circulating the regenerated potassium chloride to the step (1) to be used as a template agent to continuously prepare the capacitance carbon material.

The nitrogen adsorption-desorption curve and the pore distribution curve of the capacitance carbon material prepared in step (3) of this embodiment are shown in fig. 12 and 13, respectively, and as can be seen from fig. 12 and 13, the capacitance carbon material has a high specific surface area and rich pores; the specific surface area of the capacitance carbon material is 1157m²The pore diameter is mainly distributed between 2 and 40 nm.

Example 6

The embodiment provides a method for preparing capacitance carbon by using chloride as a template and recycling the template, wherein the method comprises the following steps:

(1) weighing 25g of potassium chloride, 10g of coal tar pitch and 10g of potassium hydroxide, and fully and uniformly mixing;

(2) placing the mixture in a porcelain boat, placing the porcelain boat in a horizontal tube furnace, introducing Ar into the furnace, simultaneously raising the temperature of the horizontal tube furnace to 750 ℃ at a temperature rise rate of 10 ℃/min, and keeping the temperature for 60min so as to calcine the mixture;

(3) naturally cooling the furnace temperature of the horizontal tube furnace to room temperature, taking out a black product, placing the black product in a dilute hydrochloric acid solution, carrying out reflux acid washing for 1h to remove a potassium chloride template agent, drying the obtained product at 100 ℃, and obtaining the capacitance carbon material after the drying is finished; the dilute hydrochloric acid solution is prepared by firstly calculating the dosage of concentrated hydrochloric acid (the mass concentration is 36% -38%) with the required standard concentration according to the amount of potassium hydroxide used in the embodiment 6 and then mixing the concentrated hydrochloric acid with the standard concentration and distilled water according to the ratio of 1: 3;

(4) and (3) evaporating and crystallizing the pickling solution obtained by pickling, drying the obtained crystal to obtain regenerated potassium chloride, and circulating the regenerated potassium chloride to the step (1) to be used as a template agent to continuously prepare the capacitance carbon material.

The nitrogen adsorption-desorption curve and the pore distribution curve of the capacitance carbon material prepared in the step (3) of the embodiment are respectively shown in fig. 14 and 15, and the specific surface area of the capacitance carbon material is 1450m²(ii)/g, pore size distribution of 2-30 nm.

Example 7

The embodiment provides a method for preparing capacitance carbon by using chloride as a template and recycling the template, wherein the method comprises the following steps:

(1) weighing 10g of sodium chloride, 10g of waste tire pyrolysis oil and 10g of sodium hydroxide, and fully and uniformly mixing;

(2) placing the mixture in a porcelain boat, placing the porcelain boat in a horizontal tube furnace, introducing Ar into the furnace, simultaneously raising the temperature of the horizontal tube furnace to 750 ℃ at a heating rate of 10 ℃/min, and keeping the temperature for 60 min;

(3) naturally cooling the furnace temperature of the horizontal tube furnace to room temperature, taking out a black product, placing the black product in a dilute hydrochloric acid solution, carrying out reflux acid washing for 1h to remove a NaCl template agent, drying the obtained product at 100 ℃, and obtaining the capacitance carbon material after the drying is finished; wherein the dilute hydrochloric acid solution is prepared by firstly calculating the dosage of concentrated hydrochloric acid (with the mass concentration of 36% -38%) with the required standard concentration according to the amount of sodium hydroxide used in the embodiment 7 and then mixing the concentrated hydrochloric acid with the standard concentration and distilled water according to the ratio of 1: 3;

(4) and (3) evaporating and crystallizing the pickling solution obtained by pickling, drying the obtained crystal to obtain regenerated sodium chloride, and circulating the regenerated sodium chloride to the step (1) to be used as a template agent to continuously prepare the capacitance carbon material.

The nitrogen adsorption-desorption curve and the pore distribution curve of the capacitance carbon material prepared in the step (3) of the embodiment are respectively shown in fig. 16 and 17, and the specific surface area of the capacitance carbon material is 1350m²The pore diameter is mainly distributed between 2 and 50 nm.

Examples 5 to 5

The present embodiment provides a super capacitor, wherein the electrode material of the super capacitor is the capacitance carbon material prepared in step (3) of example 5, fig. 18 is a cyclic voltammetry curve of the capacitance carbon material as the electrode material of the super capacitor at different scanning speeds, and as can be seen from fig. 18, the cyclic voltammetry curve shows a good rectangular shape, which indicates that the capacitance curve has good capacitance characteristics.

Examples 6 to 6

The present embodiment provides a supercapacitor, wherein the electrode material of the supercapacitor is the capacitance carbon material prepared in the step (3) of the example 6, fig. 19 is a constant current charging and discharging curve of the capacitance carbon material when the capacitance carbon material is used as the electrode material of the supercapacitor, as can be seen from fig. 19, the symmetry of the constant current charging and discharging curve is good, and the capacitance at a current density of 1A/g is 225F/g.

Examples 7 to 7

The present embodiment provides a supercapacitor, wherein the electrode material of the supercapacitor is the capacitance carbon material prepared in step (3) of example 7, fig. 20 is a rate performance curve of the capacitance carbon material as the electrode material of the supercapacitor, and as can be seen from fig. 20, when the capacitance carbon material prepared in step (3) of example 7 of the present invention is used as the electrode material of the supercapacitor, the capacitor not only has ultrahigh capacity, but also has relatively small capacity attenuation with the increase of current density, which indicates that the capacitance carbon material prepared in the example of the present invention has relatively excellent rate performance as the electrode material of the supercapacitor.

In summary, the capacitance carbon material prepared by the embodiment of the invention has a high specific surface area and a developed pore structure, and when the capacitance carbon material is used as an electrode material of a super capacitor, the capacitance carbon material exhibits excellent capacitance storage characteristics.

According to the embodiment of the invention, heavy components such as chloride, petroleum asphalt, coal asphalt, waste tire pyrolysis oil and vacuum residue oil are respectively adopted as a template agent and a carbon source for the growth of capacitance carbon, a mixture of the heavy components, the chloride and an activating agent is subjected to high-temperature calcination treatment in an inert atmosphere based on a directional guide coupling in-situ activation technology, and a high-performance capacitance carbon material with high specific surface area and developed pore structure is prepared under the guide of the template agent and the activation of the activating agent; in the process of pickling and purifying the capacitance carbon material, the obtained pickling solution is a chloride solution, and after evaporation and crystallization, chloride crystals can be obtained again, so that the regeneration and the full cyclic utilization of the chloride template agent are realized; meanwhile, the method provided by the invention is green and environment-friendly, the operation condition is easy to control, and the operation cost is low.

In summary, the embodiment of the invention uses the chloride as the template agent, and the chloride can be regenerated and recycled, thereby greatly reducing the production cost of the capacitance carbon material. Meanwhile, the capacitance carbon material prepared by the embodiment of the invention has high specific surface area, developed pore structure, excellent capacitance characteristic and good application prospect in capacitors.

The above description is only exemplary of the invention and should not be taken as limiting the scope of the invention, so that the invention is intended to cover all modifications and equivalents of the embodiments described herein. In addition, the technical features and the technical inventions of the present invention, the technical features and the technical inventions, and the technical inventions can be freely combined and used.