A kind of guanidine magnetic ionic liquid and its application for removing sulfur-containing organic matter in nonpolar solution
A magnetic ionic liquid, non-polar technology, applied in the field of high-efficiency and high-selectivity extraction and removal of sulfur-containing aromatic ring compounds in non-polar solutions, can solve problems such as harsh operating conditions, polluted oil products, and environmental pollution, and achieve chemical properties The effects of stability, reduced desulfurization rate, and short extraction time
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Embodiment 1
[0029] Embodiment 1 (ionic liquid is [TMG] [FeCl 4 ] synthetic method 1):
[0030]
[0031] Weigh 11.5 g of N,N-tetramethylguanidine (0.1 mol) into a 50 ml round bottom flask, add 15 ml of acetonitrile as a solvent, place in an ice bath, control the temperature at 0°C, and stir. Measure 0.12 mol of concentrated hydrochloric acid, slowly drop it into the round bottom flask within 30 min, continue to stir for 2 h, and rotary evaporate under reduced pressure until the solvent is completely removed to obtain a white solid, namely the intermediate [TMG]Cl.
[0032] Accurately weigh 0.1mol anhydrous FeCl 3 , directly added to the above round-bottomed flask, a dark brown liquid was rapidly formed, stirred at room temperature for 4 hours, added a small amount of methanol and rotary evaporated under reduced pressure for 3 hours, and finally obtained a brownish-yellow uniform liquid, which was the product [TMG][FeCl 4 ].
Embodiment 2
[0033] Embodiment 2 (ionic liquid is [TMG] [FeCl 4 ] synthetic method 2):
[0034] Weigh 17.25g of N,N-tetramethylguanidine (0.15mol) into a 50ml round bottom flask, add 30ml of methanol as a solvent, and stir at room temperature. Measure 0.18mol of concentrated hydrochloric acid, slowly add it dropwise into a round bottom flask within 70min, continue to stir for 4h, and rotate under reduced pressure for 3h, then add 10ml of methanol and rotate under reduced pressure until the solvent is completely removed, and after vacuum drying, a white solid is obtained, namely Intermediate [TMG]Cl.
[0035] Accurately weigh 0.5mol anhydrous FeCl 3 , directly added to the above-mentioned round bottom flask, a dark brown liquid was rapidly formed, stirred at room temperature for 5 hours, added 5ml of methanol and rotary steamed under reduced pressure for 3 hours, and finally obtained a brownish-yellow uniform liquid, which was the product [TMG][FeCl 4 ].
Embodiment 3
[0036] Embodiment 3 (ionic liquid [TMG]Cl / 1.25FeCl 3 synthesis method):
[0037]
[0038] Weigh 13.8g of N,N-tetramethylguanidine (0.12mol) into a 50ml round bottom flask, add 20ml of ethanol as a solvent, place in ice bath, control the temperature below 5°C, and stir. Measure 0.14mol of concentrated hydrochloric acid, slowly drop it into the round bottom flask within 30min, continue to stir for 2h, and rotary evaporate under reduced pressure until the solvent is completely removed to obtain a white solid, the intermediate [TMG]Cl.
[0039] Accurately weigh 0.15mol anhydrous FeCl 3 , directly added to the above round-bottomed flask, a dark brown liquid was rapidly formed, stirred at room temperature for 5 hours, ultrasonically oscillated for 0.5 hours, added a small amount of methanol and rotated under reduced pressure for 2 hours, and finally obtained a dark brown uniform liquid with a color slightly darker than that of [TMG][FeCl 4], which is the product [TMG]Cl / 1.25FeC...
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