Acid-base resistant polyether modified trisiloxane surfactant as well as preparation and application thereof
A technology of surfactant and trisiloxane, which is applied in transportation and packaging, silicon organic compounds, chemical instruments and methods, etc., can solve the problems of increased surface tension, poor acid and alkali resistance stability, and limited application range, etc., to achieve unlimited Harmful substances, no biological toxicity, and the effect of simple reaction steps
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Embodiment 1
[0030]Add polyethylene glycol monomethyl ether (M.W=350) (17.5g, 50mmol), triethylamine (6.06g, 60mmol) and CH 2 Cl 2 (100mL), magnetically stirred evenly, and acryloyl chloride (4.98g, 55mmol) and CH 2 Cl 2 (30mL) was added to the constant pressure dropping funnel, then placed in an ice bath to cool down to 0°C, and then the liquid in the constant pressure dropping funnel was slowly dropped into the three-necked flask, and after the ice bath was reacted for 1 hour, the The reaction was carried out for 4 hours, and the reaction was stopped. The insoluble matter was separated by suction filtration with a Buchner funnel, the organic phase was collected, washed with acid, alkali and saturated brine in sequence until neutral, and dried with anhydrous magnesium sulfate. The organic solvent was removed under vacuum to obtain a light yellow transparent liquid which was polyethylene glycol monomethyl ether acrylate (17.98 g, 89%).
[0031] 1 HNMR (400MHz, CDCl 3 ): 6.43 (d, 1H),...
Embodiment 2
[0037] Add polyethylene glycol monomethyl ether (M.W=350) (17.5g, 50mmol), triethylamine (6.06g, 60mmol) and CH 2 Cl 2 (100mL), magnetically stirred evenly, 2-butenoyl chloride (5.75g, 55mmol) and CH 2 Cl 2 (30mL) was added to the constant pressure dropping funnel, then placed in an ice bath to cool down to 0°C, and then the liquid in the constant pressure dropping funnel was slowly dropped into the three-necked flask, reacted in the ice bath for 1 hour, and then After reacting at room temperature for 4 hours, the reaction was terminated. The insoluble matter was separated by suction filtration with a Buchner funnel, the organic phase was collected, washed twice with acid water, twice with alkaline water, washed with saturated saline until neutral, and dried over anhydrous magnesium sulfate. The organic solvent was removed under vacuum to obtain polyethylene glycol monomethyl ether crotonate (20.6 g, 91%) as a light yellow transparent liquid.
[0038] 1 HNMR (400MHz, CDCl...
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