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A kind of preparation method of ordered mesoporous carbon material

A mesoporous carbon and surfactant technology, applied in the field of mesoporous materials, can solve the problems of long time-consuming and inability to realize large-scale production, and achieve the effects of high utilization rate, simple equipment requirements, and wide source of raw materials

Active Publication Date: 2018-06-29
LANZHOU INST OF CHEM PHYSICS CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Each of these three methods has some disadvantages, such as the EISA method and the hydrothermal method cannot achieve large-scale production, while the self-assembly method in aqueous solution takes too long

Method used

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  • A kind of preparation method of ordered mesoporous carbon material
  • A kind of preparation method of ordered mesoporous carbon material
  • A kind of preparation method of ordered mesoporous carbon material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] a) Add 1.0 g of phenol into 25 mL of 0.1 mol / L NaOH aqueous solution, heat to dissolve at 70°C, add 3.5 g of 37-40% formaldehyde aqueous solution, heat and stir at 70°C for 30 minutes;

[0030] b) Dissolve 2.2 g of F127 in 25 mL of water, mix well with the solution in step a) under stirring, and continue to react at 70°C for 8 hours;

[0031] c) Slowly add 36-38% concentrated hydrochloric acid to adjust the pH to 0.9, and the color changes from deep red to brownish yellow or bright yellow;

[0032] d) Add saturated sodium chloride aqueous solution, gradually appear yellow precipitate, stop adding when there is no more precipitate;

[0033] e) Centrifuge and separate the yellow precipitate at a rate of 8000 rpm;

[0034] f) The yellow sinking band is heated in air at 100°C for 24 hours, then heat-treated at 900°C in nitrogen or argon for 3 hours, the heating rate is 1°C / min below 600°C, and 3°C / min above 600°C;

[0035] g) The obtained ordered mesoporous carbon materia...

Embodiment 2

[0039] a) Add 1.0 g of phenol into 25 mL of 0.1 mol / L NaOH aqueous solution, heat to dissolve at 70°C, add 3.5 g of 37-40% formaldehyde aqueous solution, heat and stir at 70°C for 30 minutes;

[0040] b) Dissolve 2.2 g of F127 in 25 mL of water, mix well with the solution in step a) under stirring, and continue to react at 70°C for 8 hours;

[0041] c) Slowly add 36-38% concentrated hydrochloric acid to adjust the pH to 0.9, and the color changes from deep red to brownish yellow or bright yellow;

[0042] d) Add saturated ammonium sulfate aqueous solution, gradually appear yellow precipitate, stop adding when there is no more precipitate;

[0043] e) Centrifuge and separate the yellow precipitate at a rate of 8000 rpm;

[0044] f) The yellow sinking band is heated in air at 100°C for 24 hours, then heat-treated at 900°C in nitrogen or argon for 3 hours, the heating rate is 1°C / min below 600°C, and 3°C / min above 600°C;

[0045] g) The obtained ordered mesoporous carbon materi...

Embodiment 3

[0047]a) Add 1.0 g of phenol into 25 mL of 0.1 mol / L NaOH aqueous solution, heat to dissolve at 70°C, add 3.5 g of 37-40% formaldehyde aqueous solution, heat and stir at 70°C for 30 minutes;

[0048] b) Dissolve 2.2 g of F127 in 25 mL of water, mix well with the solution in step a) under stirring, and continue to react at 70°C for 8 hours;

[0049] c) Slowly add 36-38% concentrated hydrochloric acid to adjust the pH to 0.9, and the color changes from deep red to brownish yellow or bright yellow;

[0050] d) Add saturated sodium nitrate aqueous solution, gradually appear yellow precipitate, stop adding when there is no more precipitate;

[0051] e) Centrifuge and separate the yellow precipitate at a rate of 8000 rpm;

[0052] f) The yellow sinking band is heated in air at 100°C for 24 hours, then heat-treated at 900°C in nitrogen or argon for 3 hours, the heating rate is 1°C / min below 600°C, and 3°C / min above 600°C;

[0053] g) The obtained ordered mesoporous carbon material ...

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Abstract

The invention discloses a preparation method of an ordered mesoporous carbon material. The method comprises the following steps: carrying out self-assembly on a surfactant and a polymer source to form an ordered-structure composite, lowering the solubility of the composite in the solution by using a salt solution or solid salt so as to precipitate the composite, heating the obtained precipitate in air, and carrying out high-heat treatment in nitrogen or argon to obtain the ordered mesoporous carbon material. The ordered mesoporous carbon material has a two-dimensional hexagonal structure, the space group is p6mm, the pore size is 2-5nm, and the specific area is 300-500 m<2> / g.

Description

technical field [0001] The invention relates to a method for preparing an ordered mesoporous carbon material, belonging to the technical field of mesoporous materials. Background technique [0002] Porous carbon materials have a wide range of applications in the fields of catalysis, adsorption, separation, sewage treatment, electrochemical energy conversion and storage, etc. The most commonly used porous carbon material is activated carbon, and its pore size is in the range of micropores (less than 2nm), but in some fields such as dye adsorption or drug delivery, micropores are difficult to meet the requirements, while mesoporous (2-50nm ) has better performance. Ordered mesoporous carbon has uniform pore size distribution and adjustable pore structure, so it can better meet some specific application fields. At present, there are two methods for preparing ordered mesoporous carbon. One is the hard template method, which uses ordered mesoporous silicon as a template and org...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01B32/05
CPCC01P2002/72C01P2004/03C01P2006/17
Inventor 张俊彦段有新梁爱民程锦春
Owner LANZHOU INST OF CHEM PHYSICS CHINESE ACAD OF SCI