Method for separating trace sulfamethoxazole enriched pollutants based on molecularly imprinted polymer loaded with ionic liquid metal organic framework
A metal-organic framework and sulfamethoxazole technology, applied in water pollutants, chemical instruments and methods, water/sewage treatment, etc., can solve the lack of functional active sites, adsorbents or catalysts can not achieve the desired effect, etc. problems, to achieve the effect of strong selection and recognition ability, broad prospects for industrial application, and fast mass transfer rate
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0021] Weigh 0.2212g of 2-aminoterephthalic acid and 0.1314g of zirconium tetrachloride and ultrasonically dissolve them in N,N-dimethylformamide for later use, then weigh 0.3226g of 1-allyl-3-vinyl bromide Add imidazole and 0.0625g sulfamethoxazole into a conical flask containing 20mL N,N-dimethylformamide, shake at 180rpm in a water bath at 30°C for 4h, mix with the previous stock solution, and then add 0.7709g crosslinker II Ethylene glycol methacrylate and 10 mg of initiator azobisisobutyronitrile were ultrasonically transferred to a closed polytetrafluoroethylene reactor and autoclave under nitrogen protection, and solvothermally reacted at 120°C for 24 hours, and the product was centrifuged three times with methanol , extracted by Soxhlet elution with a mixture of methanol and acetic acid at a volume ratio of 9:1 for 72 hours, and then vacuum-dried at 80° C. for 24 hours to obtain a molecularly imprinted polymer with ionic liquids immobilized in metal-organic frameworks. ...
Embodiment 2
[0024] Weigh 0.1106g of 2-aminoterephthalic acid and 0.0657g of zirconium tetrachloride and ultrasonically dissolve them in N,N-dimethylformamide for later use, then weigh 0.3226g of 1-allyl-3-vinyl bromide Add imidazole and 0.0625g sulfamethoxazole into a conical flask containing 20mL N,N-dimethylformamide, shake at 180rpm in a water bath at 30°C for 6h, mix with the previous stock solution, and then add 0.7709g crosslinker II Ethylene glycol methacrylate and 10 mg of initiator azobisisobutyronitrile were ultrasonically transferred to a closed polytetrafluoroethylene reactor and autoclave under nitrogen protection, and solvothermally reacted at 180 ° C for 24 hours. The product was subjected to N, N -Dimethylformamide was centrifuged three times, extracted by Soxhlet elution with a mixture of methanol and acetic acid at a volume ratio of 9:1 for 72 hours, and then vacuum-dried at 60°C for 24 hours to obtain molecularly imprinted polymerization of ionic liquids immobilized in m...
Embodiment 3
[0027] Weigh 0.1106g of 2-aminoterephthalic acid and 0.1314g of zirconium tetrachloride and ultrasonically dissolve them in N,N-dimethylformamide for later use, then weigh 0.2113g of 1-allyl-3-vinyl bromide Add imidazole and 0.0625g sulfamethoxazole into a conical flask containing 20mL N,N-dimethylformamide, shake at 180rpm in a water bath at 30°C for 5h, mix with the previous stock solution, and then add 0.7709g crosslinker II Ethylene glycol methacrylate and 10 mg of initiator azobisisobutyronitrile were ultrasonically transferred to a closed polytetrafluoroethylene reactor and autoclave under nitrogen protection, and solvothermally reacted at 120°C for 36 hours, and the product was centrifuged three times with ethanol , extracted by Soxhlet elution with a mixture of methanol and acetic acid at a volume ratio of 9:1 for 48 hours, and then vacuum-dried at 80° C. for 14 hours to obtain a molecularly imprinted polymer with ionic liquids immobilized in metal-organic frameworks. ...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com