US2016136634A1PendingUtilityA1

Catalyst manufacturing method

Assignee: JOHNSON MATTHEY PLCPriority: Sep 8, 2010Filed: Jan 21, 2016Published: May 19, 2016
Est. expirySep 8, 2030(~4.1 yrs left)· nominal 20-yr term from priority
B01D 2255/2092B01D 15/08B01J 23/08C10G 45/04Y10T428/2982Y10T428/2991B01J 23/06B01J 37/16C10G 2/00B01J 23/10B33Y 10/00B01J 23/40B01J 23/70B01J 37/14C10G 25/003B01J 21/04B01J 23/02C01B 21/48B01D 2255/30B01J 37/0018B01D 2255/92B01D 2257/60B01J 23/16B01D 53/8634B01J 21/12C10G 2300/205B01J 37/18B01J 37/08C22B 43/00B33Y 80/00B01J 37/0244C10G 2300/705B01D 53/0407C10G 2300/202C21B 13/00C22B 61/00B01D 2257/602B01J 37/0215C22B 9/023B01J 37/349B01J 37/341B01J 37/0009B01D 53/9436B22F 10/64B22F 10/14B22F 10/12B22F 12/41B22F 10/28B01J 35/56B33Y 70/00B01J 35/50Y02P10/25
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Claims

Abstract

A method for producing a catalyst using an additive layer method includes: (i) forming a layer of a powdered catalyst or catalyst support material, (ii) binding or fusing the powder in said layer according to a predetermined pattern, (iii) repeating (i) and (ii) layer upon layer to form a shaped unit, and (iv) optionally applying a catalytic material to said shaped unit.

Claims

exact text as granted — not AI-modified
What is claimed: 
     
         1 . A method for producing a catalyst using an additive layer method comprising:
 (i) forming a layer of a powdered catalyst or catalyst support material,   (ii) binding or fusing the powder in said layer according to a predetermined pattern,   (iii) repeating (i) and (ii) layer upon layer to form a shaped unit, and   (iv) optionally applying a catalytic material to said shaped unit.   
     
     
         2 . A method according to  claim 1  wherein the powdered material is a catalyst powder. 
     
     
         3 . A method according to  claim 2  wherein the catalyst powder comprises a metal powder or a powdered metal compound. 
     
     
         4 . A method according to  claim 2  wherein the catalyst powder comprises one or more metals or metal compounds containing metals selected from the group consisting of Na, K, Mg, Ca, Ba, Al, Si, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Ru, Rh, Pd, Ag, Sn, Sb, La, Hf, W, Re, Ir, Pt, Au, Pb, or Ce. 
     
     
         5 . A method according to  claim 2  wherein the catalyst powder comprises a precious metal catalyst powder, comprising one or more of Pt, Pd, Ir, Ru or Re. 
     
     
         6 . A method according to  claim 2  wherein the catalyst powder comprises a transition metal compound selected from a metal oxide, metal hydroxide, metal carbonate, metal hydroxycarbonate or mixture thereof. 
     
     
         7 . A method according to  claim 6  wherein the transition metal oxide comprises a single or mixed metal oxide or a composition comprising two or more transition metal oxides. 
     
     
         8 . A method according to  claim 2  wherein the catalyst powder further comprises one or more inert materials. 
     
     
         9 . A method according to  claim 8  wherein the inert materials are selected from the group consisting of alumina, silica, silicon nitride, silicon carbide, carbon and mixtures thereof. 
     
     
         10 . A method according to  claim 2  wherein the catalyst powder comprises a zeolite. 
     
     
         11 . A method according to  claim 1  wherein the powdered material is a catalyst support powder and the method comprises applying a catalytic material to said shaped unit. 
     
     
         12 . A method according to  claim 11  wherein the catalyst support powder comprises one or more inert materials. 
     
     
         13 . A method according to  claim 12  wherein the inert materials are selected from the group consisting of alumina, silica, silicon nitride, silicon carbide, carbon and mixtures thereof. 
     
     
         14 . A method according to  claim 11  wherein the catalyst support powder comprises one or more transition metal compounds, including lanthanide metal compounds and actinide metal compounds, selected from one or more metal oxides, metal hydroxides, metal carbonates, metal hydroxycarbonates or mixture thereof. 
     
     
         15 . A method according to  claim 14  wherein the transition metal compound comprises a single or mixed metal oxide or a composition comprising two or more transition metal oxides. 
     
     
         16 . A method according to  claim 12  wherein the catalyst support powder comprises an alumina, metal-aluminate, silica, alumino-silicate, titanic, zirconia, zinc oxide, or a mixture thereof. 
     
     
         17 . A method according to  claim 11  wherein the catalyst support powder comprises a metal powder. 
     
     
         18 . A method according to  claim 17  wherein the metal powder comprises a precious metal powder or a non-precious metal powder. 
     
     
         19 . A method according to  claim 18  wherein the non-precious metal powder comprises a ferritic alloy or steel. 
     
     
         20 . A method according to  claim 11  wherein the catalyst support powder comprises a zeolite. 
     
     
         21 . A method according to  claim 11  wherein the catalytic material applied to the shaped unit comprises a metal, metal compound or a zeolite. 
     
     
         22 . A method according to  claim 21  wherein the metal is applied to the shaped unit by metal vapour deposition. 
     
     
         23 . A method according to  claim 21  wherein the metal, metal compound or zeolite is applied to the shaped unit from a solution or dispersion of the metal, metal compound or zeolite. 
     
     
         24 . A method according to  claim 22  wherein the metal or metal compound comprises one or more metals selected from the group consisting of Na, K, Mg, Ca, Ba, Al, Si, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Ru, Rh, Pd, Ag, Sn, Sb, La, Hf, W, Re, Ir, Pt, Au, Pb, or Ce. 
     
     
         25 . A method according to  claim 1  wherein the powdered material has an average particle size, D 50 , in the range 1 to 200 micrometres. 
     
     
         26 . A method according to  claim 1  wherein the additive layer method comprises a 3D printing, a stereolithographic or a laser sintering technique. 
     
     
         27 . A method according to  claim 1  wherein the powder in each layer is fused by a laser. 
     
     
         28 . A method according to  claim 1  wherein the powder in each layer is bound together with a binder. 
     
     
         29 . A method according to  claim 28  wherein the binder is an inorganic binder or an organic binder. 
     
     
         30 . A method according to  claim 28  wherein a burnout additive is included in the catalyst powder or binder to control the porosity of the resulting shaped unit. 
     
     
         31 . A method according to  claim 1  wherein the shaped unit is subjected to a heating step. 
     
     
         32 . A method according to  claim 1  wherein the shaped unit, comprising one or more reducible metal compounds, is subjected to a reduction step. 
     
     
         33 . A method according to  claim 32  wherein the reducing step is performed by exposing the shaped unit to a hydrogen-containing gas stream at a temperature in the range 150 to 800° C. 
     
     
         34 . A method according to  claim 33  wherein the reduced metal in the shaped unit is passivated by controlled exposure of the shaped unit to an oxygen-containing gas stream to form a passivating layer on said reduced metal. 
     
     
         35 . A method according to  claim 1  wherein the shaped unit is a wireframe structure or a skeletal framework containing a void space within which may have multiple internal strengthening rods. 
     
     
         36 . A catalyst obtained by the method of  claim 1 . 
     
     
         37 . A process using a catalyst according to  claim 36  comprising contacting a reactant mixture with the catalyst shaped unit under conditions to effect a catalysed reaction or sorption. 
     
     
         38 . A process according to  claim 37  comprising a catalysed reaction selected from hydroprocessing including hydrodesulphurisation, a hydrogenation, steam reforming including pre-reforming, catalytic steam reforming, autothermal reforming and secondary reforming and reforming processes used for the direct reduction of iron, catalytic partial oxidation, a water-gas shift including isothermal-shift, sour shift, low-temperature shift, intermediate temperature shift, medium temperature shift and high temperature shift reactions, a methanation, a hydrocarbon synthesis by the Fischer-Tropsch reaction, methanol synthesis, ammonia synthesis, ammonia oxidation and nitrous oxide decomposition reactions, or selective oxidation or reduction reactions of internal combustion engine or power station exhaust gases. 
     
     
         39 . A process according to  claim 37  comprising a sorption selected from the recovery of sulphur compounds or heavy metals such as mercury and arsenic from contaminated gaseous or liquid fluid streams, or particulate matter from the exhaust gases of internal combustion engines or power stations.

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