Title of Invention

A PROCESS FOR THE PREPARATION OF A BIMETALLIC CATALVST

Abstract

This invention relates to a process for preparing a bimetallic catalyst in the form of a ternary nitride of Group VIII metal and a Group VIB metal promoted with one or more metals of Group IA and IIA. The ternary nitride has a formula M°XM"yN wherein M' is a Group VIB metal, M" is a Group VIII metal and x and y are from 1 to 10 oxidic ternary nitride precursor is prepared by mixing a solution containing Group VIII metal with a solution containing Group VIB metal, nitriding the same with ammonia and adding a solution containing the promoter metals.

Full Text

The present invention relates to synthesis of ammonia from ammonia synthesis gas and in particular to a catalyst being highly active in the ammonia synthesis. Industrial preparation of ammonia is most usually performed by contacting hydrogen and nitrogen containing synthesis gas with catalyst at a pressure in the range of 100-400 bar and temperatures between 300°C and 600°C. Widely used catalysts contain iron, typically promoted with oxides of aluminium and magnesium, plus oxides of calcium and potassium to increase heat resistance and synthesis activity. Furthermore, ammonia synthesis catalysts containing other Group VIII metal compounds are known in the art. WO 96/38222 discloses a catalyst for synthesis of aimnonia in presence of a catalyst comprising Group VIII metal clusters supported on basic zeolite support. Use of ruthenium containing catalysts in the synthesis of ammonia from synthesis gas is disclosed in US patent No. 4,600,571, JP patent publication No. 9168739 and GB patent No. 2,033,776. Furthermore, molybdenum oxycarbonitride as active catalyst in the ammonia synthesis is mentioned in US patent Nos. 4,271,041 and 4,337,232, Bimetallic ammonia synthesis catalysts consisting of nickel-molybdenum are described in Z. Elektrochem. Vol. 36, Pages 690-692, 1930. It has now been found that bimetallic catalysts comprising a combination of a Group VIII metal and a Group VIB (CAS version) metal improve activity in the synthesis of ammonia from ammonia synthesis gas, when being in the nitride form. In accordance with the above observation, this invention provides a process for the preparation of ammonia from am-monia synthesis gas by contacting the synthesis gas with a bimetallic catalyst comprising ternary compounds of a Group VIII metal and a Group VIB metal at conditions being effective in the formation of ammonia, wherein the bimetallic catalyst is in its nitride form at contact with the synthesis gas. When operating the inventive process the catalyst will typically be arranged as fixed bed in an ammonia converter. The catalyst may thereby be loaded in its oxidised form which by contact with hydrogen and nitrogen and ammonia in the reacting synthesis gas is converted to the active nitride form according to the following reaction scheme: In the above general formula of the catalyst M' represents a group VIB metal, M" a group VIII metal and x and y is a mixed number between 1 and 10. Still improved catalytic activity has been observed when promoting the inventive catalyst with one or more metals selected form Group lA and IIA. At present, preferred metals for use in the above process include iron, cobalt and nickel as Group VIII metals. Molybdenum is a preferred Group VIB metal. Caesium and barium are preferred as Group lA and Group IIA promoter metals, respectively. Suitable promoters are additionally lanthanide metals. Furthermore, the invention provides a catalyst being active in the synthesis of ammonia from ammonia synthesis gas, which catalyst is a ternary nitride having the general formula optionally promoted with one or more metals selected from Group lA, IIA and the lanthanides. Operation conditions of the catalyst and the above ammonia synthesis-process are conventional and known to those skilled in the art. The invention will become more apparent from the following examples explaining in more detail preparation and operation of the catalyst and ammonia synthesis process according to specific embodiments of the invention. Example 1 Preparation of oxidic CoMo precursor. An aqueous solution containing Co(N03)2 (0.1 mole) is added dropwise to an aqueous solution containing 0.1 mole Mo as (NH4) 6MO7024-4H2O. After completion of the addition, the reaction mixture is evaporated to dryness and dried at 110°C. The product is calcined for 4 h at 600°C under air and was analysed by XRPD to be pure C0M0O4- Example 2 Preparation of oxidic NiMo precursor. Preparation of NiMo04 according to Example 1 using Ni(N03)2 instead of Co(N03)2 - Example 3 Preparation of oxidic NiMo precursor-Preparation of Ni2Mo3011 according to Example 2 using 0.066 mole Ni(N03)2 instead of 0.1 mole Ni(N03)2- Example 4 Preparation of oxidic CoMo precursor. Preparation of C04M0O7 according to Example 1 using 0.4 mole Co(N03)2 instead of 0.1 mole Co(N03)2. Example 5 Preparation of oxidic FeMo precursor. Preparation of Fe2Mo30i2 according to Example 3 using 0.066 mole Fe(N03)3 instead of 0.066 mole Ni(N03)2. Preparation of Coo.9oBao.ioMo04 according to Example 1 using 0.09 mole Co(N03)2ancl 0.010 mole Ba (NO3) 2 instead of 0.10 mole Co(N03)2. Example 9 Preparation of lanthanum promoted oxidic NiMo precursor. Preparation of Nio.85Lao.o5Mo04 according to Example 1 using 0.085 mole Ni(N03)2 and 0,005 mole La{N03)3 instead of 0.10 mole Co(N03)2. Example 10 Nitridation of oxidic CoMo precursor in pure ammonia. C0M0O4 from Example 1 is pressed into pellets, crushed and sieved to a particle size of 0.3-0.8 mm 5.0 g of material is place in the reactor described in A. Nielsen: An Investigation on Promoted Iron Catalysts for the Synthesis of Ammonia, Gjellerup 1968. The catalyst is heated in a 50 1/h stream of gaseous ammonia at 0.1°C/min to 650. It is kept at 650°C for 24 h and cooled to room-temperature. Example 11 Nitridation of oxidic CoMo precursor in diluted ammonia. This experiment is conducted as the above experiment 10 except that the nitridation is performed in a 50 1/h flow of 4.5% ammonia in 71.6% hydrogen and 23.9% nitrogen. Example 12 Nitridation of oxidic NiMo precursor in diluted ammonia. This experiment is conducted as Example 11 except that 3.1 g of NiMo04 from Example 2 is used as a starting material. Example 13 Nitridation of non-oxidic CoMo precursor in diluted ammonia. This experiment is conducted as Example 11 except that 4.3 g of Co (NH3) eMo (CN) 8 is used as a starting material. Example 17 Supported Cs promoted CoMo catalyst. The impregnation was conducted as in Example 16 except that a final impregnation with aqueous CsOH was performed to obtain 4.1% Cs on the catalyst precursor. Example 18 Testing of catalytic ammonia synthesis activity. The testing was performed in the equipment used for the intridation studies mentioned in Example 10. In all test experiments between 3-8 g of catalyst was loaded into the reactor. All catalysts were nitrided using the procedures of Example 10-12 prior to testing. The catalysts were tested at 400°C and 100 bar total pressure. The inlet gas contained 4.5% ammonia in a 3:1 hydrogen-nitrogen mixture. The flow rate was adjusted to obtain 12% ammonia in the exit. Typical flow rates were between 2000 ml/h and 50 1/h. The examples refer to the method of the precursor preparation and the activation procedure, respectively. The activity is based on the mass of catalyst loaded into the reactor. Example 19 The testing was performed as in Example 18, but with a 4.5% ammonia in a 1:1 hydrogen-nitrogen mixture. ^ The examples refer to the method of the precursor preparation and the activation procedure, respectively. The activity is based on the mass of catalyst loaded into the reactor. Comparison Example 20 High surface area molybdenum nitride M02N was prepared according to Boudart et al. (Stud. Surf. Sci. Catal. Vol 16 page 147) resulting in a surface area of 130 . A test of this catalyst by a procedure as described in the above Example 18 revealed an ammonia production activity of 20 Nml/g'h 1. Process for the preparation of ammonia from ammonia synthesis gas by contacting the synthesis gas with a ternary nitride of a Group VIII metal and a Group VIB metal at conditions being effective in the formation of ammonia. 2. Process according to claim 1, wherein the bimetallic catalyst is promoted with one or more metals selected from Group lA and IIA. 3- Process according to claim 1, wherein the catalyst includes iron, cobalt or nickel as Group VIII metals and molybdenum as Group VIB metal. 4. Process according to claim 2, wherein the Group lA catalyst promoter is caesium and the Group IIA promoter is barium. 5. Process according to claim 2, wherein the bimetallic catalyst is promoted with one or more metals selected form the lanthanides. 6. Catalyst being active in the synthesis of ammonia from ammonia synthesis gas being in form of a ternary nitride and having the general formula: wherein M'represents a Group VIB metal, M" a Group VIII metal and x and y each is a mixed number between 1 and 10. 7. Catalyst according to claim 6, wherein the Group VIII metal is selected from iron, cobalt, nickel and mixtures thereof and the Group VIB metal is molybdenum and/or tungsten- 8* Catalyst according to claim 6 further including a promoter selected from Group lA and Group IIA metals. 9. Catalyst according to claim 8, wherein the Group lA metal is caesium and the group IIA metal is barium. Catalyst according to claim 6 further including a promoter selected from lanthanide metals. 11. Process for the preparation of ammonia from ammonia synthesis gas, substantially as herein described and exemplified.

Documents:

209-mas-2000-abstract.pdf

209-mas-2000-claims filed.pdf

209-mas-2000-claims grand.pdf

209-mas-2000-correspondence others.pdf

209-mas-2000-correspondence po.pdf

209-mas-2000-description complete filed.pdf

209-mas-2000-description complete grand.pdf

209-mas-2000-form 1.pdf

209-mas-2000-form 19.pdf

209-mas-2000-form 26.pdf

209-mas-2000-form 3.pdf

209-mas-2000-form 5.pdf

209-mas-2000-other documents.pdf