Claims
- 1. A crystalline metal silicate which is substantially free of aluminum having a composition in terms of mole ratios as follows:
- 0.8.+-.0.4M.sub.2/n O:W.sub.2 O.sub.3 :5 to 500 SiO.sub.2 :O to 100 H.sub.2 O where M is a cation, n is the valence of said cation and W.sub.2 O.sub.3 is a metal oxide, said metal silicate having the X-ray diffraction pattern set forth in Table 1 of the specification prepared by the method which comprises preparing a reaction mixture which is substantially free of aluminum ions and which contains tetraalkylammonium compound, sodium hydroxide, an oxide of the desired metal, an oxide of silicon, water and an aluminum chelating agent effective to provide a catalytically active crystalline metal silicate, maintaining the mixture at an elevated temperature until crystals said metal silicate are formed and separating and recovering said crystals, and in terms of mole ratios falling within the following ranges, the reaction mixture contains:
- ______________________________________OH.sup.- /SiO.sub.2 .05-3R.sub.4 N.sup.+ /(R.sub.4 N.sup.+ + Na.sup.+) 0.1-1H.sub.2 O/OH.sup.- 10-500SiO.sub.2 /W.sub.2 O.sub.3 5-500SiO.sub.2 /Chelating agent 1-1000______________________________________
- wherein R is propyl.
- 2. A crystalline metal silicate according to claim 1 wherein the metal is boron and the aluminum content is an amount of less than about 100 wppm based on the weight of silica in the reaction mixture.
- 3. A crystalline metal silicate according to claim 2 wherein the chelating agent is selected from the group consisting of ethylene diamine tetraacetic acid, nitriliotriacetic acid and 8-hydroxyquinoline.
- 4. A crystalline metal silicate according to claim 3 wherein the chelating agent is ethylene diamine tetraacetic acid.
- 5. An activated crystalline metal silicate prepared by an activation method which comprises:
- (1) heat treating the dried silicate composition of, claim 1 at about 200.degree. to 900.degree. C.;
- (2) treating the heated silicate with a reducing agent for about 1 to 80 hours at about 200.degree. to 900.degree. C.; and
- (3) heat treating the reduced silicate following the procedure of step (1),
- said activated crystalline metal silicate having a nitrogen isotherm adsorption capacity as shown in FIG. 2.
- 6. An activated crystalline metal silicate according to claim 5 wherein the silicate heat treated in step (1) is in the hydrogen ion form.
Parent Case Info
This is a continuation of application Ser. No. 092,127, filed Nov. 7, 1979, now Pat. No. 4,331,641.
US Referenced Citations (6)
Continuations (1)
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Number |
Date |
Country |
Parent |
92127 |
Nov 1979 |
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