Method for producing glyoxylate through oxydehydrogenation of glycollate
A technology of glycolic acid ester and glyoxylic acid ester, which is applied in the direction of carboxylic acid ester preparation, chemical instruments and methods, metal/metal oxide/metal hydroxide catalyst, etc., and can solve the problem of oxidative dehydrogenation to produce glyoxylic acid ester  issues of low sex
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Embodiment 1
[0028] Prepare and stir 200ml solution I of ammonium molybdate and ammonium metavanadate containing 5.6% molybdenum and 1.4% vanadium, add 100g of alumina carrier to solution I and stir evenly to obtain slurry II, then mix 50ml iron-containing 6.6% ferric nitrate solution was slowly added dropwise to the slurry II, and then the pH was adjusted to 8 with nitric acid and ammonia water to obtain the slurry IV; after aging the slurry IV at 80°C for 8 hours, vacuum-evaporated to dryness at 90°C, and then roasted at 500°C The catalyst C1A was obtained, and the catalyst sample was taken for X-fluorescence (XRF) characterization test to determine the catalyst components. The results are shown in Table 1.
Embodiment 2
[0030] Prepare and stir 200ml solution I of ammonium molybdate and ammonium metavanadate containing 2.7% molybdenum and 1.4% vanadium, add 100g of alumina carrier to solution I and stir evenly to obtain slurry II, and then mix 50ml iron-containing 6.6% ferric nitrate solution was slowly added dropwise to the slurry II, and then the pH was adjusted to 8 with nitric acid and ammonia water to obtain the slurry IV; after aging the slurry IV at 80°C for 8 hours, vacuum-evaporated to dryness at 90°C, and then roasted at 500°C Catalyst C2A was obtained, and the catalyst sample was taken for XRF characterization test. The test results are shown in Table 1.
Embodiment 3
[0032] Prepare and stir 200ml solution I of ammonium molybdate and ammonium metavanadate containing 0.1% molybdenum and 0.05% vanadium, add 100g of alumina carrier into solution I and stir evenly to obtain slurry II, and then mix 50ml iron-containing 6.6% ferric nitrate solution was slowly added dropwise to the slurry II, and then the pH was adjusted to 8 with nitric acid and ammonia water to obtain the slurry IV; after aging the slurry IV at 80°C for 8 hours, vacuum-evaporated to dryness at 90°C, and then roasted at 500°C Catalyst C3A was obtained, and a catalyst sample was taken for XRF characterization test. The test results are shown in Table 1.
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