Synthesis method of porous ionic liquid for removing NOx in flue gas
A technology of ionic liquids and synthesis methods, applied in separation methods, chemical instruments and methods, organic compounds/hydrides/coordination complex catalysts, etc., can solve problems such as cumbersome preparation processes, and achieve simple workflow and mild reaction conditions , the effect of less dosage
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Embodiment 1
[0035] 2.0gN-butyl imidazole and 2.20g n-bromobutane are added in the three-necked flask, N 2As a protective gas, it was heated to reflux in an oil bath at 60°C and stirred for 7h. Evaporate in vacuo at 40°C to remove excess n-bromobutane, and cool to room temperature. Use diethyl ether as the extractant and apply vigorous stirring to remove residual N-methylimidazole. The solvent was evaporated and dried under vacuum for 4h to obtain viscous liquid [BMIM]Br. Equimolar lithium bis(trifluoromethanesulfonyl)imide (LiNTf 2 ) was slowly added to 2.0g [BMIM]Br, and after electromagnetic stirring at room temperature for 2h, it was extracted with chloroform (10mL×3). The organic phase was evaporated in vacuo at 90°C to obtain a viscous liquid [BMIM][NTf 2 ].
[0036] At room temperature, 2.97g Zn(NO 3 )·6H 2 O and 2.46 g of 2-methylimidazole were respectively dissolved in 100 mL of methanol, then, the two solutions were mixed and stirred continuously for 15 hours. Subsequentl...
Embodiment 2
[0039] 2.0gN-butyl imidazole and 2.20g n-bromobutane are added in the three-necked flask, N 2 As a protective gas, it was heated to reflux in an oil bath at 60°C and stirred for 7h. Evaporate in vacuo at 40°C to remove excess n-bromobutane, and cool to room temperature. Use diethyl ether as the extractant and apply vigorous stirring to remove residual N-methylimidazole. The solvent was evaporated and dried under vacuum for 4h to obtain viscous liquid [BMIM]Br. Equimolar lithium bis(trifluoromethanesulfonyl)imide (LiNTf 2 ) was slowly added to 2.0g [BMIM]Br, and after electromagnetic stirring at room temperature for 2h, it was extracted with chloroform (10mL×3). The organic phase was evaporated in vacuo at 90°C to obtain a viscous liquid [BMIM][NTf 2 ].
[0040] At room temperature, 2.97g Zn(NO 3 )·6H 2 O and 2.46 g of 2-methylimidazole were respectively dissolved in 100 mL of methanol, then, the two solutions were mixed and stirred continuously for 15 hours. Subsequent...
Embodiment 3
[0043] 2.0gN-butyl imidazole and 2.20g n-bromobutane are added in the three-necked flask, N 2 As a protective gas, it was heated to reflux in an oil bath at 60°C and stirred for 7h. Evaporate in vacuo at 40°C to remove excess n-bromobutane, and cool to room temperature. Use diethyl ether as the extractant and apply vigorous stirring to remove residual N-methylimidazole. The solvent was evaporated and dried under vacuum for 4h to obtain viscous liquid [BMIM]Br. Equimolar lithium bis(trifluoromethanesulfonyl)imide (LiNTf 2 ) was slowly added to 2.0g [BMIM]Br, and after electromagnetic stirring at room temperature for 2h, it was extracted with chloroform (10mL×3). The organic phase was evaporated in vacuo at 90°C to obtain a viscous liquid [BMIM][NTf 2 ].
[0044] At room temperature, 2.97g Zn(NO 3 )·6H 2 O and 2.46 g of 2-methylimidazole were respectively dissolved in 100 mL of methanol, then, the two solutions were mixed and stirred continuously for 15 hours. Subsequent...
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