Method for preparation of a group 4 metal silicate and use thereof

Patent metadata

Field	Value
Publication number	US-9764315-B2
Application number	US-201414785184-A
Country	US
Kind code	B2
Filing date	Apr 16, 2014
Priority date	Apr 17, 2013
Publication date	Sep 19, 2017
Grant date	Sep 19, 2017

Abstract

The invention provides a method for the preparation of an amorphous silicate of at least one metal from the Group 4 of the Periodic Table of Elements with a total pore volume of at least 0.3 mL/g. The method of preparation involves the use of pore shaping conditions, which can be the use of a pore shaper and optionally an increased precipitation temperature, e.g. at least 60° C. The silicate of the invention is especially suitable in catalytic reactions such as esterifications, Michael additions, transesterifications, (ep)oxidations, hydroxylations, or in adsorbance of small inorganic and organic molecules e.g. CO 2 or aromatic compounds.

First claim

The invention claimed is:

1. Method for the preparation of a mesoporous and/or macroporous amorphous Group 4 metal silicate with the general formula
M v+ w T x Si y O 2x+2y+0.5vw ,

wherein M is selected from the group consisting of a proton, ammonium, a metal cation and combinations thereof, v is the valence of M being a positive integer, T is at least one of the Group 4 metals, x, y and w are molar ratios:
x is 1;
y is from 0.01 to 99;
w is from 0.01 to 50; and

wherein said silicate has a total pore volume of at least 0.3 mL/g as measured by liquid nitrogen adsorption, comprising the steps of:
(a) providing a metal source of at least one metal of Group 4, a silicate source and optionally a pore shaper in an aqueous medium;
(b) carrying out a precipitation reaction by combining the metal and the silicate sources and having a pH range of 7-8.5, whereby a substance of the metal silicate and a soluble salt are formed; and
(c) drying the substance to remove water,

wherein the preparation is performed under pore shaping conditions, wherein said pore shaping conditions consists of the use of a pore shaper before the drying step (c),
wherein a halide salt of M is formed in the precipitation reaction or is added before, during or after the precipitation reaction in step (b), which halide salt is then replaced by a non-halide salt before drying, which non-halide salt is allowed to accumulate in the substance during step (c).

2. The method according to claim 1 , wherein the pore shaping conditions further consists of the use of a temperature of at least 60° C. during the precipitation in step (b).

3. The method according to claim 1 , wherein the pore shaper is a soluble salt of M, wherein M is selected from the group consisting of a proton, ammonium, a metal cation and combinations thereof.

4. The method according to claim 3 , wherein M is selected from the group consisting of a proton, ammonium, Na, Li, K, Cs, Ca, Mg, Sr, Ba, Fe, Sn, Ce, La, Nb, Ni, V, W, Mo, Al, Ag, Zn, Cu, Mn cations, and combinations thereof.

5. The method according to claim 1 , wherein said non-halide salt is selected from the group consisting of phosphate, biphosphate, phosphite, biphosphite, sulfate, bisulfate, sulfite, bisulfite, nitrate, nitrite, carbonate, bicarbonate, formate, acetate and citrate.

6. The method according to claim 1 , wherein T is selected from the group consisting of Ti, Zr and Hf, and mixtures thereof.

7. The method according to claim 1 , wherein the metal source of at least one metal of Group 4 is a soluble salt, wherein said salt is a halide salt or a non-halide salt.

8. The method according to claim 1 , wherein the metal source of at least one metal of Group 4 is a titanium source selected from the group consisting of TiCl 4 , titanium(IV) oxychloride, titanium(IV) bromide, titanium(IV) fluoride, titanium(IV) iodide, titanium(IV) alkoxides, TiO-alkoxides and Ti(III) compounds.

9. The method according to claim 1 , wherein the silicate source is a soluble metal silicate or an organic silicate.

10. The method according to claim 1 , comprising a calcination step of the metal silicate.

11. The method according to claim 1 , wherein after step (c), the salt is then removed from the metal silicate in a washing step followed by a further drying step.

12. The method according to claim 1 , wherein said method comprises an ion exchange step before or after drying step (c), and wherein said ion exchange step is performed with cations.

Assignees

• Basf Corp

Inventors

• Brandts Jim Aloysius Maria
• Wagemaker Lorianne

Classifications

• C02F2101/006

  Radioactive compounds · CPC title

• C02F2101/20

  Heavy metals or heavy metal compounds · CPC title

• C02F1/42

  by ion-exchange (ion-exchange in general B01J) · CPC title

• C11C3/10

  Ester interchange · CPC title

• B01J29/89 Primary

  Silicates, aluminosilicates or borosilicates of titanium, zirconium or hafnium {(B01J29/005 takes precedence)} · CPC title