Patent classifications
B01J23/85
Hydroprocessing co-catalyst compositions and methods of introduction thereof into hydroprocessing units
A hydroprocessing co-catalyst composition may comprise in an embodiment a first component comprising co-catalyst particles and a liquid carrier, and a second component comprising a dispersant and a dispersant diluent. The co-catalyst particles may be in the micron size range, and the dispersant may promote dispersion of the co-catalyst particles in materials such as the liquid carrier, the dispersant diluent, and combinations thereof. Methods of introducing a hydroprocessing co-catalyst composition into a hydroprocessing system are also disclosed.
Hydroprocessing co-catalyst compositions and methods of introduction thereof into hydroprocessing units
A hydroprocessing co-catalyst composition may comprise in an embodiment a first component comprising co-catalyst particles and a liquid carrier, and a second component comprising a dispersant and a dispersant diluent. The co-catalyst particles may be in the micron size range, and the dispersant may promote dispersion of the co-catalyst particles in materials such as the liquid carrier, the dispersant diluent, and combinations thereof. Methods of introducing a hydroprocessing co-catalyst composition into a hydroprocessing system are also disclosed.
CATALYST SUPPORT AND CATALYSTS PREPARED THEREFROM
A supported catalyst useful in processes for chemically refining hydrocarbon feedstocks is prepared, the catalyst comprising a metal from Group 6 of the Periodic Table, a metal from Groups 8, 9 or 10 and optionally phosphorous, wherein the metals, and phosphorous when present, are carried on a foraminous carrier or support, the carrier or support, preferably comprises porous alumina having a total pore volume (TPV) of about 0.6 cc/g to about 1.1 cc/g and comprising: (a) equal to or greater than about 78% to about 95% of TPV in pores having a diameter of less than about 200 Angstroms (); (b) greater than about 2% to less than about 19% of the TPV in pores having a diameter of about 200 () to less than about 1000 ; (c) equal to or greater than 3% to less than 12% of the TPV in pores having a diameter equal to or greater than about 1000 ; and (d) a pore mode equal to or greater than about 90 and less than about 160 . Preferably the support exhibits a d50 greater than about 100 and less than about 150 .
Catalyst for selective hydrogenation of dienes, preparation method and application thereof
A mixed metal oxide catalyst for selective hydrogenation of dienes comprising a Group VIII metal, a trivalent metal, a Group IA metal, a Group IVB metal, a Group IIB metal, two Group VIB metals and SiO.sub.2Al.sub.2O.sub.3 as balance. The catalyst comprises 10-40 wt % of Group VIII metal, 5-30 wt % of trivalent metal, 0.1-8 wt % of Group IA metal, 0.1-8 wt % of Group IVB metal, 0.1-30 wt % of Group IIB metal, 5-50 wt % of two Group VIB metals and 10-30 wt % of SiO.sub.2Al.sub.2O.sub.3, based on the catalyst in terms of oxide, and has 150-300 m.sup.2/g of specific surface area, 0.4-0.8 ml/g of pore volume.
Ammoxidation catalyst for propylene, manufacturing method of the same catalyst, ammoxidation method using the same catalyst
An ammoxidation catalyst includes a metal oxide represented by Chemical Formula 1 supported on a silica carrier, wherein the catalyst has pores having a diameter of 5 to 200 nm, a pore volume of 0.1 to 3.0 cm.sup.3/g, and a BET surface area of 50 m2/g to 1,000 m2/g:
Mo.sub.12Bi.sub.aFe.sub.bA.sub.cB.sub.dC.sub.eO.sub.xChemical Formula 1 wherein in Chemical Formula 1, A is one or more elements of Ni, Mn, Co, Zn, Mg, Ca, and Ba, B is one or more elements of Li, Na, K, Rb, and Cs, C is one or more elements of Cr, W, B, Al, Ca, and V, and a to e, and x are respectively fractions of each atom or atomic group, wherein a is 0.1 to 5, b is 0.1 to 5, c is 0.1 to 10, d is 0.1 to 2, e is 0 to 10, and x is 24 to 48.
Ammoxidation catalyst for propylene, manufacturing method of the same catalyst, ammoxidation method using the same catalyst
An ammoxidation catalyst includes a metal oxide represented by Chemical Formula 1, wherein a first peak having intensity of A appears in the 2 range of 26.3=0.5, and a second peak having intensity of B appears in the 2 range of 28.30.5 in X ray diffraction analysis by CuK, and an intensity ratio (A/B) of the first peak to the second peak is 1.5 or more:
Mo.sub.xBi.sub.aFe.sub.bA.sub.cB.sub.dC.sub.eD.sub.fO.sub.yChemical Formula 1 wherein in Chemical Formula 1, A and B are different from each other, and each independently, are one or more elements of Ni, Mn, Co, Zn, Mg, Ca, and Ba, C is one or more elements of Li, Na, K, Rb, and Cs, D is one or more elements of Cr, W, B, Al, Ca, and V, a to f, x, and y are respectively mole fractions of each atom or atomic group, a is 0.1 to 7, b is 0.1 to 7, provided that the sum of a and b is 0.1 to 7, c is 0.1 to 10, d is 0.01 to 5, e is 0.1 to 10, f is 0 to 10, x is 11 to 14, y is a value determined by each oxidation number of Mo, Bi, Fe, A, B, C, and D.
Catalyst to attain low sulfur gasoline
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.
Catalyst to attain low sulfur gasoline
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.
Production of renewable diesel and propylene
Feeds containing triglycerides are processed to produce a diesel fuel product and propylene. The diesel product and propylene are generated by deoxygenating the triglyceride-containing feed using processing conditions that enhance preservation of olefins that are present in the triglycerides. The triglyceride-containing feed is processed in the presence of a catalyst containing a Group VI metal and a Group VIII non-noble metal and in the presence of CO.
Method for selective hydrogenation of unsaturated compound
The present invention relates to a method for the selective hydrogenation of an unsaturated compound, particularly a method in an unsaturated compound or a mixture containing unsaturated compounds for increase of the light sulphides weight, hydrogenation of a polyunsaturated compound and isomerization of a monounsaturated compound. The method uses a supported catalyst. The supported catalyst contains at least one Group VIB non-noble metal oxide and at least one Group VIII non-noble metal oxide deposited on a carrier; and the catalyst has an optimized acid distribution on the surface of the catalyst, and more preferably has an optimized Group VIII/VIB metal ratio and a Group VIII non-noble metal density per unit of catalyst surface area.