Method for extracting and separating phenolic compound in oil-phenol mixture by using quaternary ammonium dication liquid
A phenolic compound, dication technology, applied in the field of phenolic compounds
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Embodiment 1
[0021] In this example, phenol and toluene are respectively selected as the analog components of phenolic compounds and oil in the oleophenol mixture. First, add 150.00g of phenolic compound to a beaker containing toluene, stir to dissolve, transfer it to a 500mL volumetric flask, add toluene, shake well and dilute to obtain a simulated oleophenol mixture. The concentration of the compound is 300.00g / L.
[0022] Take 20mL of the above simulated oleylphenol mixture in a 50mL graduated test tube, and add 12.4323g of 1,2-bis(N-triethyl)-1,2-dibromoethane salt, 1,2-bis(N- The molar ratio of triethyl)-1,2-dibromoethane salt [molecular weight is 390g / mol] to phenolic compounds is 0.5, and then placed in a water bath at 25°C and magnetically stirred for 30 minutes, standing for 20 minutes, using a separatory funnel After phase separation, 17.2 mL of phenol-removed oil phase and 3.5 mL of eutectic solvent were obtained.
[0023] The composition of the dephenolic oil phase was analyzed by...
Embodiment 2
[0027] In this example, phenol and toluene are respectively selected as the analog components of phenolic compound and oil in the oleophenol mixture. First, add 50.00g of phenolic compound to a beaker containing toluene, stir to dissolve, transfer it to a 500mL volumetric flask, add toluene, shake well, and dilute to obtain a simulated oleophenol mixture. The concentration of the compound is 100.00g / L.
[0028] Take 20mL of the above-mentioned simulated oleophenol mixture into a 50mL graduated test tube, and add 0.8288g of 1,2-bis(N-triethyl)-1,2-dibromoethane salt, 1,2-bis(N- The molar ratio of triethyl)-1,2-dibromoethane salt [molecular weight is 390g / mol] to phenolic compounds is 0.1, and then placed in a 60℃ water bath and magnetically stirred for 30 minutes, standing for 20 minutes, using a separatory funnel After phase separation, 19.5 mL of the phenol-removed oil phase and 0.8 mL of the eutectic solvent were obtained.
[0029] The composition of the dephenolic oil phase wa...
Embodiment 3
[0033] In this example, phenol and n-hexane are respectively selected as the analog components of phenolic compounds and oil in the oleophenol mixture. First, add 5.00g of phenolic compound to a beaker containing n-hexane, stir to dissolve, transfer it to a 500mL volumetric flask, add n-hexane to it, shake well, and dilute to obtain a simulated oleophenol mixture. The concentration of phenolic compounds is 10.00 g / L.
[0034] Take 20mL of the above simulated oleylphenol mixture in a 50mL graduated test tube, and add 1.6577g of 1,2-bis(N-triethyl)-1,2-dibromoethane salt, 1,2-bis(N- The molar ratio of triethyl)-1,2-dibromoethane salt [molecular weight is 390g / mol] to phenolic compounds is 2.0, and then placed in a 0℃ water bath and magnetically stirred for 30 minutes, standing for 20 minutes, using a separatory funnel Phase separation was performed to obtain 19.5 mL of the phenol-removed oil phase and 0.6 mL of the eutectic solvent.
[0035] An ultraviolet-visible spectrophotometer...
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