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Middle-pore carbon material and its preparation method

A technology of porous carbon and carbon coating, which is applied in chemical instruments and methods, carbon preparation/purification, and other chemical processes, and can solve problems such as limitations, high-temperature residual carbon rate, and failure of porous carbon to provide effective examples.

Inactive Publication Date: 2013-02-13
PEKING UNIV +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, this method fails to provide an effective example for the preparation of porous carbons with large mesopore diameters in the range of 20nm-50nm.
2. The magnesium gluconate and magnesium citrate template precursors used in the Inagaki method have a relatively high high-temperature carbon residue rate, resulting in the final porous carbonization of pure magnesium gluconate or magnesium citrate even without mixing any other carbon precursors. The mesopore wall thickness of carbon products can only be nano-scale thickness, and the adjustment to the direction of thinner pore wall is completely limited by the method itself

Method used

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  • Middle-pore carbon material and its preparation method
  • Middle-pore carbon material and its preparation method
  • Middle-pore carbon material and its preparation method

Examples

Experimental program
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Effect test

Embodiment 1

[0076] 1) Nano magnesium oxide powder (specific surface area 369m 2 / g) 4.6g, resorcinol 1.4g, furfural 1.7g, ethanol 50mL, after mixing, carry out polymerization reaction at 90 ° C for 3 hours, after the reaction is completed, resin-coated magnesium oxide is obtained, and then it is dried;

[0077] 2) In an inert atmosphere, the resin-coated magnesia obtained in step 1) is heated from room temperature to 1000° C. for 3 hours at a heating rate of 5° C. / min to carbonize to obtain charcoal-coated magnesia;

[0078] 3) Remove the magnesium oxide template from the carbon-coated magnesium oxide obtained in step 2) with 1mol / L sulfuric acid, filter, wash the solid product with deionized water until neutral, and dry to obtain the mesoporous carbon provided by the present invention.

[0079] The BET specific surface area of ​​the mesoporous carbon is 2618m 2 / g, nitrogen adsorption total pore volume 2.7cm 3 / g, t-map microporosity is less than 1%, the average pore diameter is 4.2nm,...

Embodiment 2

[0081] 1) Nano magnesium oxide powder (specific surface area 401m 2 / g) 5.2g, resorcinol 3.0g, mass percentage concentration is 3.2g of formaldehyde aqueous solution 37%, ethanol 45mL after mixing, carry out polymerization reaction at 90 ℃ for 3 hours, after the reaction is completed, resin-coated magnesium oxide is obtained. then dry it;

[0082] 2) In an inert atmosphere, the resin-coated magnesia obtained in step 1) is heated from room temperature to 1000° C. for 3 hours at a heating rate of 5° C. / min to carbonize to obtain charcoal-coated magnesia;

[0083] 3) Remove the magnesium oxide template from the carbon-coated magnesium oxide obtained in step 2) with 2mol / L hydrochloric acid, filter, and wash the solid product with deionized water until neutral. Dry to obtain mesoporous carbon.

[0084] The BET specific surface area of ​​the mesoporous carbon is 1975m 2 / g, nitrogen adsorption total pore volume 2.4cm 3 / g, t-map microporosity is less than 1%, the average pore d...

Embodiment 3

[0086] 1) Nano magnesium oxide powder (specific surface area 401m 2 / g) 5.2g, resorcinol 3.0g, benzaldehyde 4.2g, ethanol 50mL and then carry out polymerization reaction at 90 ℃ for 3 hours, after the reaction is completed, resin-coated magnesium oxide is obtained, and then it is dried;

[0087] 2) In an inert atmosphere, the resin-coated magnesia obtained in step 1) is heated from room temperature to 1000° C. for 3 hours at a heating rate of 5° C. / min to carbonize to obtain charcoal-coated magnesia;

[0088] 3) Remove the magnesium oxide template from the carbon-coated magnesium oxide obtained in step 2) with 1 mol / L sulfuric acid, filter, and wash the solid product with deionized water until neutral. Dry to obtain mesoporous carbon.

[0089] The BET specific surface area of ​​the mesoporous carbon is 1782m 2 / g, nitrogen adsorption total pore volume 1.6cm 3 / g, t-map microporosity is less than 5%, the average pore diameter is 3.7nm, and the most probable pore diameter is ...

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Abstract

The invention discloses a middle-pore carbon material and its preparation method. The method comprises the following steps: 1, uniformly mixing an aldehyde compound, a phenolic compound and a magnesium oxide template, and carrying out a polymerization reaction to obtain resin coated magnesium oxide; 2, carbonizing the resin coated magnesium oxide obtained in step 1 through heating in an inert atmosphere to obtain carbon coated magnesium oxide; and 3, dissolving magnesium oxide through uniformly mixing the carbon coated magnesium oxide obtained in step 2 with an acid in order to obtain the middle-hole carbon material. The highest specific surface area and the highest middle-pore pore volume of the middle-pore carbon material provided by the invention can exceed 2600m<2> / g and 5.5cm<3> / g respectively under a condition that the middle pore rate of the middle-pore carbon material exceeds 95%; and the method has obvious advantages unmatched by known technologies in the regulation of the pore diameter distribution, the pore wall thickness and the like of the middle-pore carbon material, and deserves the wide popularization and application in the catalytic field, the adsorption field, the electrode material field and the like.

Description

technical field [0001] The invention belongs to the field of advanced nanoporous materials and technologies, and specifically relates to a mesoporous carbon material and a preparation method thereof. Background technique [0002] According to the classification of the International Union of Pure and Applied Chemistry (IUPAC), the pores in porous carbon materials can be divided into micropores (pore diameter<2nm), mesopores (2-50nm) and macropores (>50nm). The pore size distribution of traditional activated carbon materials is mainly in the micropore range, and the specific surface area is generally 500-1500m 2 / g, the pore volume is generally less than 1cm 3 / g, its application in emerging high-tech fields is limited by the small aperture. [0003] After the 1970s, the technology of preparing so-called super activated carbon (Super activated carbon) by the chemical activation method represented by the potassium hydroxide activation method appeared, and industrial pro...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C01B31/02B01J20/20B01J2/30C01B32/05
Inventor 朱月香隗罡王羽谢有畅
Owner PEKING UNIV