Multi-branch cationic phosphonium salt, forward osmosis extract containing it, and forward osmosis seawater desalination process
A cationic, phosphonium salt technology, used in osmotic/dialysis water/sewage treatment, seawater treatment, water treatment parameter control, etc., can solve the problems of difficulty in removing magnetic nanoparticles, high energy consumption, and difficult re-dispersion of magnetic particles.
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preparation example 1
[0079] 1,8-Octanediyl-bis(tri-n-butylphosphonium)bis(p-toluenesulfonate)(P2-TOS)
[0080] First, synthesize 1,8-octanediyl-bis(tri-n-butylphosphonium) dibromide (1,8-octanediyl-bis(tri-n-butylphosphonium) dibromide) (hereinafter referred to as P2-Br):
[0081] (1) Take a 500mL round bottom bottle, put 80g (0.4mol) of tributylphosphine and 48.9g (0.18mol) of 1,8-dibromooctane (1,8-dibromooctane), and then add anhydrous Acetone 150mL was stirred at 40°C for 48 hours.
[0082] (2) After the reaction, slowly drop the above solution into 1.5L ether. The resulting white powder solid was filtered and washed several times with ether.
[0083] (3) The washed white solid was dried to obtain 117 g of the product P2-Br.
[0084] Next, 1,8-octanediyl-bis(tri-n-butylphosphonium)di(p-toluenesulfonate) was synthesized (hereinafter referred to as P2-TOS):
[0085] (1) Dissolve 2.67 g (3.7 mmol) of P2-Br and 1.57 g (8.1 mmol) of sodium p-toluenesulfonate (TOS-Na) in 13 g of deionized water...
preparation example 2
[0091] 1,8-Octanediyl-bis(tri-n-butylphosphonium)bis(2,4,6-trimethyl-benzenesulfonate)(P2-TMBS)
[0092] Synthesis of 1,8-octanediyl-bis(tri-n-butylphosphonium)bis(2,4,6-trimethyl-benzenesulfonate)(1,8-octanediyl-bis(tri-n-butylphosphonium) di(2,4,6-trimethyl-benzenesulfonate)) (hereinafter referred to as P2-TMBS):
[0093] (1) Dissolve 10g (14.7mmol) of P2-Br and 6.8g (29.6mmol) of 2,4,6-trimethylbenzenesulfonate (sodium2,4,6-trimethyl-benzenesulfonate) (TMBS-Na) in 40 g of deionized water, stirred at room temperature for 24 hours.
[0094] (2) After the reaction was completed, 20 mL of ethyl acetate was added for extraction.
[0095] (3) The organic layer was concentrated to obtain about 12.4 g of the product P2-TMBS.
[0096] The product P2-TMBS was determined via NMR ( 1 H-NMR, 400MHz, at D 2 O): 0.8(t,18H,CH 3 CH 2 -), 1.09(m,4H,-CH 2 -), 1.1~1.5(m,32H,-CH 2 -), 1.9~2.0(t,16H,PCH 2 -), 2.12(s,6H,Ar-CH 3 ), 2.25(s,12H,Ar-CH 3 ), 6.88 (s, 4H, ArH). The chemical...
preparation example 3
[0099] Trimethylolpropane tris[(tri-n-butylphosphonium)butyrate]tris(p-toluenesulfonate)(P3-TOS)
[0100] First, trimethylolpropanetris(4-bromobutyrate) is synthesized:
[0101] (1) Take a 50 mL round-bottomed reaction bottle, put 1 g (8.3 mmol) of trimethylolpropane (trimethylolpropane), dissolve it with 20 mL of anhydrous tetrahydrofuran (tetrahydrofuran; THF), then slowly add 1.1 g of NaH (60%), After stirring with a magnet at room temperature for 2 hours, 5 g (27 mmol) of 4-bromobutyryl chloride (4-bromobutyryl chloride) was added dropwise and reacted overnight at room temperature.
[0102] (2) Drain THF after the reaction is finished, add 20 mL of ether, filter the solution to remove solids, wash the obtained filtrate three times with 50 mL of water, and then drain the product to obtain 3.4 g of the product trimethylolpropane trimethylolpropane (4-Bromobutyrate).
[0103] Next, synthesize trimethylolpropane tris[(tri-n-butylphosphonium)butyrate]tribromide (trimethylolpr...
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