Preparation method of dibasic alcohol dicarboxylic acid ester
A technology of dihydric alcohol dicarboxylate and dihydric alcohol is applied in the preparation of dihydric alcohol dialkyl benzoate and the field of dihydric alcohol dibenzoate, which can solve the problem of reduced catalytic activity and poor performance. It can effectively solve the problems of catalyst refinement and deactivation, and achieve the effect of high conversion rate and selectivity, less circulating materials and strong atom economy.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0045] The present invention provides a kind of preparation method of dibasic alcohol dicarboxylate, comprising: in the presence of catalyst, dibasic alcohol and benzoic acid and / or alkyl benzoic acid are contacted and reacted, and the water generated by reaction is removed simultaneously; The catalyst is a bulk phase catalyst containing silicon, tin and oxygen and contains Sn-O-Si bonds.
[0046] According to the present invention, the dihydric alcohol is diethylene glycol, triethylene glycol, 2,2'-dihydroxydipropyl ether (dipropylene glycol), ethylene glycol, 1,3-propanediol and 1,3-butanediol one or more of them.
[0047] According to the present invention, under reflux state, the reaction is performed for 2h-10h, preferably for 3h-6h.
[0048] According to the present invention, the molar ratio of acid to alcohol is (1:0.4)˜(1:0.9), preferably (1:0.52)˜(1:0.6).
[0049] According to the present invention, as a means to adjust the reflux and / or a measure to protect the re...
preparation Embodiment 1
[0097] Get 2.26g stannous chloride dihydrate (SnCl 2 2H 2 O) be dissolved in 10ml deionized water, get Na 2 O SiO 2 9H 2 O was dissolved in deionized water. Add the two solutions into the flask at the same time at 30°C, feed the Si / Sn ratio to 1, add ammonia solution to adjust the pH value to 6, after the precipitation is complete, keep it at 50°C for 2 hours, filter, wash with water, °C, and then baked at 300 °C for 3 hours under the protection of nitrogen to obtain the tin catalyst of the present invention, code A.
[0098] According to XRF analysis, the Si / Sn molar ratio of the catalyst is 0.96.
[0099] According to XPS analysis, the atomic mass fraction of tin on the surface of the catalyst is 5.12%; through ICP analysis, the mass fraction of tin in the catalyst is 63.5%.
preparation Embodiment 2
[0101] Get 2.26g stannous chloride dihydrate (SnCl 2 2H 2 O) be dissolved in 80ml concentration and be in the hydrochloric acid aqueous solution of 1mol / L, take Na 2 O SiO 2 9H 2 O was dissolved in deionized water. Add the two solutions into the flask at the same time at 30°C, feed the Si / Sn ratio of 5, add ammonia solution to adjust the pH value to 7, after the precipitation is complete, continue to keep at 30°C for 2 hours, filter, wash, and dry at 80°C °C, and then baked at 250 °C for 4 hours under the protection of nitrogen to obtain the tin catalyst of the present invention, code B.
[0102] According to ICP analysis, the mass fraction of tin in the catalyst is 27.2%.
PUM
| Property | Measurement | Unit |
|---|---|---|
| quality score | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


