HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522934Generated: November 4, 2026
Azane;molybdenum;tetracosahydrate → Molybdenum
https://huagongshe.com/reaction/1522934
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azane;molybdenum;tetracosahydrate | HCID 25488 | — |
| Solvent | Water | HCID 962 | — |
| Product | Molybdenum | HCID 23932 | — |
| Product | Azane;molybdenum;tetracosahydrate | HCID 25488 | — |
Reaction Steps
The catalyst of this Example was prepared in a similar manner as described in Example 6. An ammoniumheptamolybdate solution was prepared by dissolving 4.63 g of ammoniumheptamolybdate in 20 mL of deionized water and adjusting the volume to 25 mL to provide a solution with a molybdenum concentration of 0.15 mol/L. The zeolite was subjected to impregnation as a powder without shaping. The zeolite, 10 g, was impregnated with a solution comprising 6.4 mL of the ammoniumheptamolybdate solution and 2.7 mL of deionized water. The zeolite powder and the solution were manually mixed with a spatula. The impregnated support was dried and calcined by placing it in an oven and heating it with dry air (1 L/min) at a rate of 1° C./min to 70° C. and holding for 10 hours. Then the temperature was increased to 120° C. at a rate of 1° C. per minute and held for 10 hours. Finally, the temperature was increased to 500° C. at a rate of 1° C. per minute and held for 5 hours. The finished catalyst was sieved to remove fines and to obtain the desired 315-500 microns fraction. The catalyst had a molybdenum content of 6.0% wt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09079169B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-e0e26918d1b147f1b55833151297af58 |
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| Source note | uspto-grants-2015_07 |
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