Catalyst of methyl glycolate hydrogenation to produce ethylene glycol, and preparation method and application of the catalyst
A technology of methyl glycolate and catalyst, which is applied to the catalyst and preparation field of the hydrogenation of methyl glycolate to ethylene glycol, can solve the problems of poor stability of the catalyst, high cost of raw materials, easy high temperature sintering, etc. The effect of low product generation, low cost and not easy inactivation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0040] Weigh 21.26g of lanthanum nitrate and dissolve it in 20ml of water to prepare solution I, weigh 100g of alumina and 40g of titanium oxide and add it to solution I to prepare mixture II, knead and dry mixture II with 3.5ml of dilute nitric acid and 65ml of water to prepare Obtain mixture III, roast mixture III at 1050 DEG C to obtain the lanthanum-modified carrier; take by weighing 64.47g of nickel nitrate and 26.78g of cobalt nitrate and dissolve in 60ml of water to obtain solution IV, take by weighing 2.5g of ethylenediamine and Dissolve 5g of polyethylene glycol-2000 in 12ml of ethanol to make solution V; place solutions IV, V and the previously prepared carrier in a crystallization kettle for aging at 60°C for 4 hours, and then adjust the pH of the crystallization kettle with ammonium bicarbonate The value is 7.5. After filtering and washing, it is dried at 120°C for 2 hours and roasted at 350°C for decomposition. Introduce hydrogen at a space velocity of 1000m 3 / m ...
Embodiment 2
[0042] Weigh 10.63g of lanthanum nitrate and dissolve it in 20ml of water to make solution I, weigh 60g of alumina and 80g of zirconia and add it to solution I to make mixture II, knead and dry mixture II with 5ml of dilute nitric acid and 52ml of water to prepare Mixture III, roast mixture III at 1100°C to obtain a lanthanum-modified carrier; weigh 79.83g of nickel nitrate and 19.01g of copper nitrate and dissolve them in 60ml of water to prepare solution IV, weigh 3.1g of P123 and 1.8g of polyethylene Diol-2000 was dissolved in 15ml ethanol to make solution V; solution IV, V and the previously prepared carrier were placed in a crystallization kettle for aging at 90°C for 3 hours, and then ammonium bicarbonate was used to adjust the pH of the crystallization kettle to 9.0. After filtering and washing, dry at 120°C for 2 hours, and roast and decompose at 390°C. Introduce hydrogen at a space velocity of 1000m 3 / m 3 h -1 Under the conditions, the temperature was programmed t...
Embodiment 3
[0044] Weigh 15.95g of lanthanum nitrate and dissolve it in 20ml of water to make solution I, weigh 135g of alumina and add it to solution I to make mixture II, knead and dry mixture II with 4.0ml of dilute nitric acid and 60ml of water to make mixture III , roasting mixture III at 1150°C to obtain a lanthanum-modified carrier; weigh 55.74g of nickel nitrate and 21.54g of zinc nitrate in 60ml of water to prepare solution IV, weigh 4.5g of TMB and 3.2g of ethylenediamine in Prepare solution V with 10ml of ethanol; place solutions IV, V and the previously prepared carrier in a crystallization tank for aging at 80°C for 4 hours, then use ammonium bicarbonate to adjust the pH of the crystallization tank to 8.0, filter and wash, and dry at 120°C 2h, 460 ℃ roasting decomposition. Introduce hydrogen at a space velocity of 1000m 3 / m 3 h -1 Under the conditions, the temperature was programmed to rise to 420°C, kept for 8 hours, and the catalyst was prepared after cooling down. Acc...
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