A method for efficiently removing nitrogen compounds in oil products
A technology for nitrogen compounds and oil products, which is applied in the field of removing nitrogen compounds in oil products by using polysulfonate ionic liquid, can solve the problems of limited nitrogen compound removal capacity, difficulty in non-basic nitrogen removal, and high agent-oil ratio. Achieve mild reaction conditions, high acid density, and small agent-oil ratio.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0028] 1) Preparation of ionic liquid:
[0029] a) After mixing 1,4-butane sultone and triphenylphosphine in a molar ratio of 1:1, place it in a microwave reactor, and set it at 90 o After C reacted for 30 minutes, carry out vacuum filtration and wash with anhydrous acetone for 2 times, carry out vacuum drying to obtain substance M;
[0030] b) Mix substance M and 98wt% concentrated sulfuric acid at room temperature in a molar amount of 1:4, put it into a microwave reactor, and heat it at 120 o The reaction was carried out under the condition of C for 30 min, and then the polysulfonate ionic liquid was obtained by vacuum filtration, washing with anhydrous acetone for 2 to 3 times, and vacuum drying.
[0031] Put 1g of ionic liquid sample into a glass reactor with magnetic stirring, and then add 400mL of quinoline simulated oil with a nitrogen content of 250mg / L, stir and react at room temperature for 20min, settle for 30min and absorb the upper layer Use TNS-3000 nitrogen an...
Embodiment 2
[0033] 1) Preparation of ionic liquid:
[0034] a) Mix 1,4-butane sultone and triphenylphosphine in a molar ratio of 1:1 and place it in a microwave reactor. o After C was reacted for 2 hours, it was then vacuum-filtered and washed with anhydrous acetone for 3 times, then vacuum-dried to obtain substance M;
[0035] b) Mix substance M and 98wt% concentrated sulfuric acid at a molar ratio of 1:4 at room temperature, put it into a microwave reactor, and heat it at 120 o The reaction was carried out under the condition of C for 30 min, and then vacuum filtration was carried out, washed with anhydrous acetone for 2 to 3 times, and then vacuum-dried to obtain the polysulfonate ionic liquid.
[0036] Put 1g of ionic liquid sample into a glass reactor with magnetic stirring, and then add 400mL of pyridine simulated oil with a nitrogen content of 250mg / L to it, stir and react at room temperature for 30min, and absorb the upper layer of oil after static settlement for 30min Use TNS-3...
Embodiment 3
[0038] 1) Preparation of ionic liquid
[0039] 1) Mix 1,4-butane sultone and triphenylphosphine in a molar ratio of 1:1 and place it in a microwave reactor. o After C reacted for 80 hours, carry out vacuum filtration and wash with anhydrous acetone, and carry out vacuum drying to obtain substance M;
[0040] 2) Mix substance M with 98wt% concentrated sulfuric acid at room temperature in a molar ratio of 1:4, put it into a microwave reactor, and heat it at 120 o The reaction was carried out under the condition of C for 30 min, and then vacuum filtration was carried out, washed with anhydrous acetone for 2 to 3 times, and then vacuum-dried to obtain the polysulfonate ionic liquid.
[0041] Put 1g of ionic liquid sample into a glass reactor with magnetic stirring, then add 400mL simulated oil of quinoline and pyridine mixture with a nitrogen content of 250mg / L, stir and react at room temperature for 25min, and settle After 30 minutes, absorb the upper layer of oil and use TNS-3...
PUM

Abstract
Description
Claims
Application Information

- Generate Ideas
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com