A kind of crude oil demulsifier and preparation method thereof
A technology of crude oil demulsifier and demulsifier, which is applied in chemical dehydration/demulsification, treatment of hydrocarbon oil, petroleum industry, etc. It can solve the problems of secondary pollution and poor environmental friendliness of demulsifier, and achieve a neat and strong oil-water interface. Competitive adsorption capacity, good effect of safe use
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Embodiment 1
[0049] Prepare the N-n-butyrylation carboxymethyl chitosan of polyethylene glycol monomethyl ether graft, concrete steps are as follows:
[0050] (1) Synthesis of N-acylated chitosan: 2g chitosan (CS) (M w =179.17kDa, degree of deacetylation >95%, viscosity 100-200mPa·s) dissolved in 40mL of 10% acetic acid aqueous solution, added 160mL of methanol to dilute, added 5.9mmol of n-butyric anhydride under stirring conditions, and stood at room temperature for 24h Add 260mL of acetone as precipitating agent, precipitate is washed three times respectively with methanol and ether, and freeze-dried to obtain white water-soluble solid N-n-butyrylated chitosan (A 4 CS).
[0051] Wherein the consumption of n-butyric anhydride is 0.5 times of the amount of amino substance contained in chitosan, and concrete calculation method is as follows:
[0052] The sugar unit of chitosan is glucosamine residue, and the molecular weight of this residue (sugar unit of chitosan) is 161, and the amount...
Embodiment 2
[0057] Prepare the N-n-hexanoylated carboxymethyl chitosan grafted with polyethylene glycol monomethyl ether, the specific steps are as follows:
[0058] (1) Synthesis of N-acylated chitosan: 2g chitosan (CS) (M w =179.17kDa, deacetylation degree>95%, viscosity 100~200mPa·s) was dissolved in 40mL 10% acetic acid aqueous solution, added 160mL methanol to dilute, under stirring condition, add n-hexanoic anhydride 5.9mmol according to the amount of amino substance 0.5 times, in Placed at room temperature for 24 hours, 260 mL of acetone was added as a precipitant, the precipitate was washed three times with methanol and ether, and freeze-dried to obtain a white water-soluble solid N-n-hexanoylated chitosan (A 6 CS). Wherein the calculation method of n-hexanoic anhydride consumption is described in step (1) with reference to embodiment 1.
[0059] (2) Carboxymethylation of N-n-hexanoylated chitosan: get 1.128g A 6 Add 100mL of distilled water to CS in a 250mL three-neck flask, a...
Embodiment 3
[0063] Prepare the N-octanoyl carboxymethyl chitosan grafted with polyethylene glycol monomethyl ether, and the specific steps are as follows:
[0064] (1) Synthesis of N-acylated chitosan: 2g chitosan (CS) (M w =179.17kDa, degree of deacetylation>95%, viscosity 100-200mPa·s) dissolved in 40mL of 10% acetic acid aqueous solution, added 160mL of methanol for dilution, and added 5.9mmol of n-octylic anhydride according to 0.5 times the amount of amino substances under stirring conditions, After standing at room temperature for 24 h, 260 mL of acetone was added as a precipitating agent, and the precipitate was washed three times with methanol and ether, and freeze-dried to obtain a white water-soluble solid N-octanoyl chitosan (A 8 CS). Wherein the calculating method of n-octanoic anhydride consumption is described with reference to step (1) among the embodiment 1.
[0065] (2) Carboxymethylation of N-octanoyl chitosan: get 1.256g A 8 Add 100mL of distilled water to CS in a 25...
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