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A kind of composite adsorbent and its preparation method and application

A composite adsorption and template technology, applied in the chemical industry, can solve the problems of easy escape and even decomposition of organic amines, and achieve the effects of high adsorption capacity and effective utilization of amines, improved thermal stability, and mild conditions.

Inactive Publication Date: 2017-01-11
CHENGDU UNIV OF INFORMATION TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In addition, organic amines are easy to escape or even decompose during multiple cycles of adsorption / desorption

Method used

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  • A kind of composite adsorbent and its preparation method and application
  • A kind of composite adsorbent and its preparation method and application
  • A kind of composite adsorbent and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] At 50°C, stir and dissolve 4.80g of cetyltrimethylammonium bromide (CTAB) in 240.00g of deionized water; add 5.72g of tetraethoxysilane (TEOS) and continue stirring for 30min before adding 0.49 g of γ-mercaptopropyltriethoxysilane and 0.25 g of H 2 o 2 (30wt%), then added dropwise 25% ammonia solution to adjust the pH to about 10.5, and after continuing to stir for 2h, the resulting white emulsion was put into a 200ml hydrothermal kettle, and reacted at 100°C for 24h. With 300ml ethanol-hydrochloric acid solution ( ) was repeatedly refluxed three times to remove the templating agent. Finally, it was dried under vacuum at 60°C overnight, and this was the modified MCM-41 carrier, which was designated as 7SBA-15. Stir and dissolve 2.00g polyethyleneimine (PEI) and 1.00g tetraethylenepentamine (TEPA) in 40ml of methanol solution at room temperature, then add the above-mentioned modified carrier material according to the amine loading of 50wt%, and continue stirring for ...

Embodiment 2

[0041] Under the condition of 50°C, stir and dissolve 12.00g CTAB in 25.33g deionized water; then add 0.45g NaOH, continue stirring for 30min, then add 4.26g tetraethoxysilane, 0.41g mercaptopropylmethyldimethoxy silane, 5.15g of H 2 o 2 (30wt%). Stirring was continued for 1 h, and the obtained white emulsion was put into a 200 ml hydrothermal kettle, and reacted at 100° C. for 48 h. With 500ml ethanol-hydrochloric acid solution ( ) was repeatedly refluxed three times to remove the templating agent. Finally, it was dried under vacuum overnight at 80° C., and this was the modified MCM-48 carrier, denoted as 10MCM-48. Stir and dissolve 3g of pentaethylenehexamine (PEHA) in 40ml of methanol solution at room temperature, then add the above-mentioned modified carrier material according to the amine loading capacity of 30wt%, and continue stirring for 3h, evaporate the solvent to dryness, and then vacuum-dry at 100°C overnight. The obtained composite adsorbent is denoted as 3...

Embodiment 3

[0043] Under the conditions of vigorous stirring at 35°C, 1.5g polyethylene glycol (PEG) was dissolved in 30g ethanol solution to form an emulsion, then 0.24g (3-mercaptopropyl) trimethoxysilane and 2.72g H 2 o 2 (30wt%), continue to stir for 45min, add dropwise 4.75g of tetraethoxysilane, use HCl (3.0g) solution to adjust the pH to about 7, and continue to stir for 24h. With 300ml ethanol-hydrochloric acid solution ( ) was repeatedly refluxed three times to remove the templating agent. Finally, it was dried under vacuum overnight at 100° C., and this was the modified MCM-50 carrier, denoted as 5MCM-50. Stir and dissolve 2g of polyethylene polyamine (PEPA) in 30ml of methanol solution at room temperature, then add the above-mentioned modified carrier material according to the amine loading of 40wt%, and continue to stir for 2h, evaporate the solvent to dryness and vacuum dry at 100°C overnight. The resulting composite adsorbent is denoted as 40PEPA / 5MCM-50. The CO of thi...

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Abstract

The invention discloses a composite adsorbent with excellent heat stability and amine availability, and a preparation method and application thereof. The composite adsorbent is composed of a propyl-sulfo-modified porous support material and impregnation-supported organic polyamine, wherein the organic polyamine accounts for 20-50 wt% of the composite adsorbent. The terminal sulfonate contained in the introduced propyl-sulfo group can immobilize the organic polyamine into the support pores, thereby enhancing the stability of the composite adsorbent. The extended long carbon chain obstructs the organic polyamine into granules in space to reduce the diffusional resistance of adsorbed gas in the organic polyamine, so that the organic polyamine is sufficiently combined with the exposed amino group, thereby improving the amine availability of the composite material. The modified composite adsorbent has wide application prospects in CO2, SO2 or H2S entrapment of coal fume.

Description

technical field [0001] The invention belongs to the technical field of chemical industry, and in particular relates to an amine-modified CO with excellent thermal stability and effective utilization of amine. 2 , SO 2 or H 2 S composite adsorbent, the present invention also relates to the preparation method and application of the composite adsorbent. Background technique [0002] CO 2 , SO 2 、H 2 S and other acid gases not only endanger the growth of organisms, but also cause serious damage to buildings, resulting in huge economic losses. Therefore, effective control of acid gases in the atmosphere has become an urgent research topic. In particular, reports from the European Union's Joint Research Center and the Netherlands Environmental Assessment Agency show that my country's CO2 in 2012 2 Emissions have reached 9.1 billion tons, of which CO emissions from coal-fired power plants 2 That's 40%. Therefore, CO in the flue gas of coal-fired power plants 2 (~60-150°C)...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J20/26B01J20/30B01D53/02
CPCB01D53/02B01D2253/202B01J20/26B01J20/3085B01J2220/4812Y02C20/40
Inventor 刘洁徐成华印红玲刘盛余
Owner CHENGDU UNIV OF INFORMATION TECH