Preparation method of C5 fatty acid monosaccharide ester and application in cigarette and cigarette
A technology of monosaccharide ester and fatty acid, which is applied in the field of preparation of fatty acid monosaccharide ester, can solve the problems of inconsistent taste and affect the quality of cigarette smoke, and achieves the advantages of softening smoke, improving smoke quality and improving the dryness of smoke. Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0015] The present invention provides a kind of preparation method of saturated fatty acid monosaccharide ester, in one embodiment, comprises the steps:
[0016] (1) preparing a mixed ionic liquid, in which the volume ratio of the hydrophilic ionic liquid to the hydrophobic ionic liquid is 1:0.1 to 1:10;
[0017] (2) adding an aqueous monosaccharide solution 0.1 to 10 times the volume of the mixed ionic liquid into the mixed ionic liquid and mixing evenly, concentrating under reduced pressure at 50°C to 60°C to remove water, and then removing undissolved monosaccharides to obtain a super Saturated monosaccharide ionic liquid;
[0018] (3) Add C5 fatty acid to the supersaturated monosaccharide ionic liquid, the mass concentration of the C5 fatty acid in the supersaturated monosaccharide ionic liquid is 10-1000g / L, and then press lipase and the C5 fatty acid Add lipase at a ratio of 5 to 500 U / g to form a reaction system, add a desiccant to the reaction system to remove water, ...
Embodiment 1
[0056] 50mL hydrophilic ionic liquid [Bmim][TfO] and 50mL hydrophobic ionic liquid [Bmim][TfO] 2 N] Mix well. Add 50 g of 400 g / L glucose aqueous solution to the mixed ionic liquid. Concentrate the glucose ionic liquid mixture in a rotary evaporator at 50°C to remove water until the water content in the mixed liquid is less than 10% (mass fraction) (determined by Karl Fischer method), and then mix the undissolved glucose particles with ions The liquid was separated, and the ionic liquid layer was collected to obtain a supersaturated glucose ionic liquid mixture. Add the above-mentioned glucose ionic liquid, 8.2g of 3-methylbutyric acid, Novozyme435 (from Candida Antarctica) 410U, 10g of 4A molecular sieve into a 500ml Erlenmeyer flask with a stopper, and react on a constant temperature shaker at 40°C for 20h, calculated as 3-methylbutyric acid , The reaction conversion rate was 82%. Add 500 mL of ethyl acetate to extract 3 times, collect the ethyl acetate, distill off the e...
Embodiment 2
[0058] Mix 90mL hydrophilic ionic liquid [Bmim][TfO] with 10mL hydrophobic ionic liquid [Bmim][TfO] 2 N] Mix well. Add 40 g of 500 g / L glucose aqueous solution to the mixed ionic liquid. Concentrate the glucose ionic liquid mixture in a rotary evaporator at 50°C to remove water until the water content in the mixed liquid is less than 2% (measured by Karl Fischer method), then separate the undissolved glucose particles from the ionic liquid and collect The supersaturated glucose ionic liquid mixture was obtained from the ionic liquid layer. Add the above-mentioned glucose ionic liquid, 8.2g of 3-methylbutyric acid, Novozyme435 (from Candida Antarctica) 410U, 15g of 4A molecular sieve into a 500ml Erlenmeyer flask with a stopper, and react on a constant temperature shaker at 40°C for 20h. Calculated, the reaction conversion rate was 80%. Add 500 mL of ethyl acetate to extract 3 times, collect the ethyl acetate, distill off the ethyl acetate under reduced pressure, and collect...
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