Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
  • B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
  • B01J23/74—Iron group metals
  • B01J23/755—Nickel
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J35/00—Catalysts, in general, characterised by their form or physical properties
  • B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
  • B01J35/391—Physical properties of the active metal ingredient
  • B01J35/392—Metal surface area
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J35/00—Catalysts, in general, characterised by their form or physical properties
  • B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
  • B01J35/61—Surface area
  • B01J35/613—10-100 m2/g
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J35/00—Catalysts, in general, characterised by their form or physical properties
  • B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
  • B01J35/64—Pore diameter
  • B01J35/647—2-50 nm
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J35/00—Catalysts, in general, characterised by their form or physical properties
  • B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
  • B01J35/64—Pore diameter
  • B01J35/651—50-500 nm

Definitions

• the invention is directed to a nickel catalyst, more in particular to a nickel catalyst mainly consisting of nickel, with very advantageous structural properties.
• Nickel catalysts have been used already for a long time in various catalytic applications, such as hydrogenation and desulfu ⁇ zation. Traditionally either supported nickel catalysts or so-called Raney nickel catalysts are used.
• the supported catalyst are generally based on a ceramic support, such as silica, alumina and the like, on the surface of which an amount of nickel is present. These amounts of nickel may vary widely, from as low as 5 wt.% up to amounts of more than 75 wt.%.
• Supported catalysts have the advantage that it is relatively easy to provide a suitable catalyst structure. By first structuring the support, before applying the active material, it is possible to maintain the structure of the support. This applies especially to catalysts having a not too high nickel loading.
• Raney nickel has a high nickel content, i.e. more than 90 wt.%, but the pore sizes of Raney nickel tend to be rather small, namely typically between 4.5 and 6.5 nm, and the total pore volume is typically about 0.15 ml/g.
• the present invention is based on the surprising discovery that the use of only a small amount of a structural promoter m the preparation of high nickel content catalysts makes it possible to produce nickel catalysts having a high nickel loading, a good nickel surface area m combination with good sinter resistance and wide pores.
• the invention is accordingly directed to a nickel catalyst comprising 0.1 to 12.5 wt.% of at least one structural promoter, selected from the group of oxides of metals and metalloids and combinations thereof, and 87.5 to 99.9 wt.% of nickel, calculated on the weight of nickel and the structural promoter together, the catalyst having an nickel surface area, as defined herein, of at least 10 m 2 /g catalyst and an average pore diameter, as defined herein, of 10 to 60 nm.
• the structural promoter can be any material that provides a binding, structure promoting effect on the catalyst. More in particular, oxides of metal and metalloids are suitable, such as silica, silica-alumina, alumina, zirconia, titania, magnesia or ceria. Preferred materials are alumina, silica and silica-alumina. In the case of alumina it is preferred to use amounts, calculated on the weight of nickel (metal) and alumina of not more than 6.35 wt.%. Higher amounts are not necessary and may lead to a decrease in pore size. Most preferred amounts for the structural promoter are up to 5 wt . % . These amounts provide the possibility of a very high nickel loading in a stable material, in combination with the very advantageous pore structure.
• the structural promoter is included in the catalyst during the preparation thereof, for example by adding the structural promoter during or after the precipitation of nickel precursor, such as nickel carbonate.
• An especially suitable method comprises first precipitating the nickel precursor, ageing the precipitate and adding a solution or suspension of the (precursor) of the structural binder to the precipitate, optionally followed by further ageing. Subsequently the material is further treated to produce a catalyst, which may include drying, calcining, reducing and passivating. These steps are conventional in the preparation of nickel catalysts .
• Suitable sources for the structural promoter that may be added " during the preparation of the catalyst are clay, metasilicate, colloidal silica, waterglass and sililic acid ether.
• the type of material used as (precursor for) the structural promoter depends on the required properties of the catalyst .
• the structural promoter may influence the acid-base properties of the catalyst.
• Such a catalyst may have a very good selectivity in the hydrogenation of unsaturated fatty nitrils to produce unsaturated fatty amines, without substantial hydrogenation of the unsaturation.
• a more alkaline catalyst for example by using a silicate solution as precursor for the structural promoter.
• a silicate solution as precursor for the structural promoter.
• Such a catalyst has a better selectivity than Raney nickel towards primary amines in the hydrogenation of fatty nitriles.
• the nickel surface area of the catalyst will generally be between 10 and 65 m/g of catalyst.
• hydrogen chemisorption measurements are performed with a dynamic pulse method similar to that described and discussed by Wanke et.al. (Can. J. Chem. Eng. vol 59, June 1981, 357). From the hydrogen chemisorption the nickel surface area is calculated according to a method as described by Bartholomew et.al. (Journal of Catal. 65 (1980)
• the BET surface area as determined by single point adsorption using the BET equation (as e.g. described by G.
• Sandstede et.al., Chem. Ing. Tech. 32 (1960), 413) is in general at least 15 m 2 /g catalyst. This surface area will generally be up to about 100m 2 /g .
• the advantageous pore structure of the catalyst of the present invention is characterised by wide pores in combination with a good porosity.
• the average pore diameter of the catalyst is at least 10 nm, preferably between 10 and 60 nm. This average pore diameter is calculated from the pore volume by the formula PV*4000/SA, m which PV is the pore volume as defined underneath, and SA is the single point BET surface area. For example for silica containing materials, this is quite contrary to the usual pore size of 4 nm. At higher amounts of structural promoter, these typical values are found again.
• the macropore size does not play a role in this, which is also confirmed by the use of nitrogen physisorption for defining the average pore diameter.
• This method only determines pore diameters up to about 60 nm.
• the best definition of the shape of the pores is a cylindrical shape. Accordingly the model for determining the average pore diameter was based on this shape.
• the other aspect of the structure of the catalyst is the pore volume.
• This pore volume is the pore volume as determined with nitrogen physisorption for pores smaller than 60 nm, and will be generally be at least 0.2 ml/g of catalyst, more in particular be between 0.2 and 1.0 ml/g of catalyst. Within these ranges a mechanically strong material is obtained, having good accessibility for the reactants, without undue diffusion restrictions.
• the required values for both the pore volume and the average pore diameter can be obtained by careful selection of the production conditions, including choice of promoter, precipitation conditions, ageing conditions and the like.
• the catalyst of the invention may be based on nickel only, or may contain minor amounts (less than 2.5 wt.% on nickel) of one or more promoting metals. It is also possible to use the catalyst m sulfided form, for example for the desulfurisation of solvents.
• the catalyst of the invention may be used for all kinds of reactions for which nickel catalyst are being used, including both supported and Raney nickel catalysts.
• Examples thereof are the various hydrogenation reactions, such as hydrogenation of fatty nitrils to amines, hydrogenation of aromatic nitro compounds to produce l.a. aniline, hydrogenation of acids and aldehydes, hydrogenation of solvents and resins, desulfurisation reactions, such as desulfurisation of solvents, dehydrogenation reactions and the like.
• the invention is further elucidated on the basis of some examples .
• a nickel catalyst is prepared according to the following steps :
• the sodium carbonate solution is heated to 55 °C in a 5 dm 3 vigorously stirred stainless steel vessel in which baffles are installed to provide good agitation. Within a period of 1.5 hours the nickel solution is dosed into the sodium carbonate solution. The final pH of solution is between 7.5 and 7.8.
• the temperature of the slurry is elevated to 90°C, at which it is aged for 1 hour .
• a nickel catalyst containing a structural promoter is prepared by following step A to E as mentioned in example 1, with the following changes in step A and C:
• step A Besides the 2 solutions mentioned in example 1, in step A also the following solution is prepared:
• step A the silicate solution as mentioned in step A is added to the slurry.
• a nickel catalyst containing a structural promoter is prepared by following step A to E as mentioned in example 1, with the following changes in step A and C:
• step B also the following solution is prepared: • 30 ml sodium silicate solution, by diluting 9.4 g
• step A the silicate solution as mentioned in step A is added to the slurry.

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• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Catalysts (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
• Inorganic Compounds Of Heavy Metals (AREA)

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• 1998
  • 1998-08-28 EP EP98202878A patent/EP0985448A1/en not_active Withdrawn
• 1999
  • 1999-08-27 AU AU55347/99A patent/AU5534799A/en not_active Abandoned
  • 1999-08-27 JP JP2000567301A patent/JP4473450B2/ja not_active Expired - Fee Related
  • 1999-08-27 EP EP99941872A patent/EP1117481B1/en not_active Expired - Lifetime
  • 1999-08-27 WO PCT/NL1999/000534 patent/WO2000012210A1/en not_active Ceased
  • 1999-08-27 DK DK99941872T patent/DK1117481T3/da active
  • 1999-08-27 ES ES99941872T patent/ES2232164T3/es not_active Expired - Lifetime
  • 1999-08-27 US US09/763,846 patent/US6524994B1/en not_active Expired - Lifetime
  • 1999-08-27 AT AT99941872T patent/ATE279980T1/de not_active IP Right Cessation
  • 1999-08-27 DE DE69921347T patent/DE69921347T2/de not_active Expired - Lifetime

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