Hydroprocessing catalyst prepared with waste catalyst fines and its use
US-9211536-B2 · Dec 15, 2015 · US
US9636662B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9636662-B2 |
| Application number | US-39070609-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 23, 2009 |
| Priority date | Feb 21, 2008 |
| Publication date | May 2, 2017 |
| Grant date | May 2, 2017 |
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This invention relates to a hydrodesulfurization catalyst, a method for preparing the catalyst, and a method for the preparation of low sulfur gasoline fuel with minimal loss of RON. The catalyst particles include a group VIB metal and a support material having relatively high surface area, and optionally includes one or more group VIIIB metal. The method for preparing the catalyst allows for greater loading of the active metal species on the surface of the support material under aqueous reaction conditions.
Opening claim text (preview).
We claim: 1. A method for preparing a hydrodesulfurization catalyst consisting essentially of: placing an activated carbon catalyst support that is not acidic under vacuum; heating the activated carbon catalyst support under vacuum to a temperature of 100° C.; preparing an aqueous solution comprising molybdenum, cobalt and water; introducing, after placing the activated carbon catalyst support under vacuum, the aqueous solution to the activated carbon catalyst support, such that the aqueous solution and activated carbon catalyst support are under vacuum; removing the water from the solution under vacuum and collecting the catalyst particles; calcinating the catalyst particles by heating the particles to a temperature of greater than 200° C., the calcinated catalyst particles comprising 25 % by weight molybdenum oxide and 6 . 2 % by weight cobalt oxide; and partially sulfiding the catalyst particles by contacting the calcined catalyst particles with a liquid hydrocarbon comprising dimethyldisulfide at a temperature of 320° C.; wherein the support material has a surface area of greater than 1000 m 2 /g. 2. The method of claim 1 wherein the step of calcinating the solid catalyst particles comprises heating the particle in the presence of oxygen to a temperature greater than about 300° C. 3. The method of claim 1 wherein the molar concentration of the molybdenum and cobalt in solution is between about 0.001 and 1.5 M. 4. The method of claim 1 wherein the molar ratio of molybdenum to cobalt is between 1.5:1 and 5:1. 5. The method of claim 1 wherein the weight ratio of the oxide form of molybdenum to the activated carbon catalyst support that is not acidic is greater than about 15% by weight. 6. The method of claim 1 wherein the weight ratio of the oxide form of cobalt to the activated carbon catalyst support is between about 4% and 10% by weight. 7. The method of preparing a desulfurization catalyst consisting essentially of: placing an activated carbon catalyst support that is not acidic under vacuum; heating the activated carbon catalyst support under vacuum to a temperature of 100° C.; preparing a first mixture comprising (NH 4 )6Mo 7 O24.4H 2 O and water introducing, after placing the activated carbon catalyst support under vacuum, the first mixture to the activated carbon catalyst support, such that the aqueous solution and activated carbon catalyst support are under vacuum; removing the water under vacuum from the first mixture to produce a solid catalyst precursor; preparing a second mixture comprising Co(NO 3 ) 2 .6H 2 O, water and the solid catalyst precursor; removing the water under vacuum from the second mixture to produce catalyst particles; calcinating the catalyst particles by heating the particles in an oxygen containing atmosphere to a temperature of 320° C. at a rate of 2° C. per minute; and sulfiding the calcinated catalyst particles to a sulfur content of 2.5% by weight. 8. The method of claim 7 wherein the surface area of the active carbon catalyst support that is not acidic is about 250 m 2 /g to about 500 m 2 /g.
Chromium, molybdenum or tungsten · CPC title
characterised by the catalyst used · CPC title
Chromium, molybdenum or tungsten · CPC title
Chromium, molybdenum or tungsten · CPC title
and cobalt · CPC title
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