Acid-Resistant Alloy Catalyst
US-2017203283-A1 · Jul 20, 2017 · US
US10464870B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10464870-B2 |
| Application number | US-201515514980-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 23, 2015 |
| Priority date | Sep 28, 2014 |
| Publication date | Nov 5, 2019 |
| Grant date | Nov 5, 2019 |
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Provided is a method for preparing a diol. In the method, a saccharide and hydrogen as raw materials are contacted with a catalyst in water to prepare the diol. The employed catalyst is a composite catalyst comprised of a main catalyst and a cocatalyst, wherein the main catalyst is a water-insoluble acid-resistant alloy; and the cocatalyst is a soluble tungstate and/or soluble tungsten compound. The method uses an acid-resistant, inexpensive and stable alloy needless of a support as a main catalyst, and can guarantee a high yield of the diol in the case where the production cost is relatively low.
Opening claim text (preview).
The invention claimed is: 1. A method for preparing a diol comprising contacting a sugar and hydrogen with a catalyst in water in a reactor to prepare a diol; wherein the catalyst is a composite catalyst consisting of a main catalyst and a cocatalyst; the main catalyst is a water-insoluble acid-resistant alloy comprising nickel, one or more rare earth elements, tin and aluminum; and the cocatalyst is a soluble tungstic acid salt and/or an insoluble tungsten compound. 2. The method of claim 1 , wherein the diol is ethylene glycol. 3. The method of claim 2 , wherein the pH of the reactor is 1-7. 4. The method of claim 1 , wherein the sugar is selected from the group consisting of one or more five-carbon monosaccharides, disaccharides, and oligosaccharides; six-carbon monosaccharides, disaccharides and oligosaccharides; soluble five-carbon polysaccharides and soluble six-carbon polysaccharides. 5. The method of claim 1 , wherein the sugar is provided in the form of an aqueous sugar solution, wherein the aqueous sugar solution has a concentration of 5-60 wt %. 6. The method of claim 5 , wherein the amount of the soluble cocatalyst used is 0.01-5 wt % of the aqueous sugar solution. 7. The method of claim 6 , wherein the amount of the insoluble cocatalyst used is 0.5-50 wt % of the main catalyst. 8. The method for preparing a diol as claimed in claim 1 , characterized in that the acid-resistant alloy comprises, in parts by weight, 10-90 parts nickel, 1-5 parts rare earth element, 1-60 parts tin and 5-9 parts aluminum. 9. The method of claim 1 , wherein the acid-resistant alloy comprises, in parts by weight, 10-90 parts nickel, 1-5 parts rare earth element, 1-60 parts tin, 5-9 parts aluminum, 1-90 parts tungsten and 0.5-20 parts molybdenum. 10. The method of claim 1 , wherein the soluble tungstic acid salt is selected from the group consisting of ammonium tungstate, sodium tungstate, sodium phosphotungstate and combinations thereof. 11. The method of claim 1 , wherein the insoluble tungsten compound is selected from tungsten trioxide, tungstic acid and a combination thereof. 12. The method of claim 1 , wherein the amount of the main catalyst used is 0.01-10 times the amount of sugar fed per hour. 13. The method of claim 1 , wherein the reactor has a reaction pressure of 6-10 MPa, a reaction temperature of 180-250° C., and a reaction time of 0.5-3 h. 14. The method of claim 1 , wherein the method is continuous. 15. The method of claim 14 , wherein the amount of main catalyst added is: 0.01-5 kg of main catalyst is added per 1000 kg of sugar fed. 16. The method of claim 1 , further comprising separating the cocatalyst from the diol and then recycling the cocatylst in a subsequent method. 17. The method of claim 1 , wherein the reactor is slurry bed reactor.
Dihydroxylic alcohols · CPC title
Tungsten · CPC title
by elimination of -OH groups, e.g. by dehydration (C07C29/34 takes precedence) · CPC title
by reduction of an oxygen containing functional group · CPC title
Mixing {(B01J37/0009, B01J37/0018 take precedence)} · CPC title
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