US2023022210A1PendingUtilityA1
Metal oxides-silica composite and method for preparing the same
Est. expiryMay 3, 2039(~12.8 yrs left)· nominal 20-yr term from priority
B01J 21/08B01J 35/1019B01J 23/02B01J 37/0236B01J 35/1014B01J 37/10B01J 37/035B01J 35/1061B01J 2235/00B01J 2235/15B01J 35/70B01J 35/613B01J 21/14B01J 37/031B01J 35/615B01J 35/647
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Claims
Abstract
Metal oxides-silica composite materials are synthesized by a co-precipitation method to serve as modified catalysts for converting ethanol into four-carbon hydrocarbons. The method includes mixing a liquid-phase silicon source and a metal precursor at different ratios so as to change the acid-base composition of the composite materials and thereby increase selectivity with respect to the four-carbon products.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for preparing a metal oxides-silica composite, comprising the steps of:
titrating a basic solution with a metal precursor solution so that a titration reaction takes place between the metal precursor solution and the basic solution at a pH value greater than 7, wherein the basic solution contains a basic agent dissolved in a first solvent, the metal precursor solution contains an M 3+ salt and an N 2+ salt, both dissolved in a second solvent, and the M 3+ salt and the N 2+ salt are a trivalent metal salt and a bivalent metal salt respectively, with an N:M molar ratio of 3:1; adding a liquid-phase silicon source after completion of the titration reaction, and then allowing an aging reaction to take place, thereby obtaining a precipitate, wherein the liquid-phase silicon source is added at an N 2+ :M 3+ :Si molar ratio of 3:1:x, in which 0<x≤10; and calcinating the precipitate to obtain the metal oxides-silica composite.
2 . The method of claim 1 , wherein the M 3+ salt is an aluminum salt, and the N 2+ salt is a magnesium salt.
3 . The method of claim 2 , wherein the M 3+ salt is aluminum nitrate, and the N 2+ salt is magnesium nitrate.
4 . The method of claim 1 , wherein the basic agent is an alkali metal hydroxide.
5 . The method of claim 1 , wherein both the first solvent and the second solvent are water or aqueous alcohol solutions.
6 . The method of claim 1 , wherein the liquid-phase silicon source is selected from the group consisting of alkoxysilane, silicate, and a combination thereof.
7 . The method of claim 1 , wherein the titration reaction takes place at a pH value greater than or equal to 10.
8 . The method of claim 1 , wherein the calcinating is performed at a temperature of at least 100° C.
9 . The method of claim 8 , wherein the calcinating comprises: performing a first calcination process at least 110° C. for a first predetermined amount of time, then raising to at least 550° C. at which performs a second calcination process for a second predetermined amount of time.
10 . The method of claim 9 , wherein the first predetermined amount of time is at least 6 hours, and the second predetermined amount of time is at least 12 hours.
11 . The method of claim 1 , wherein the calcinating is performed after the precipitate is dried.Join the waitlist — get patent alerts
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