AU620248B2 - Creación de Inventos y Patentes con Inteligencia Artificial

AU620248B2 – Nickel/silica catalyst and the preparation and use thereof
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AU620248B2 – Nickel/silica catalyst and the preparation and use thereof
– Google Patents
Nickel/silica catalyst and the preparation and use thereof

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Publication number
AU620248B2

AU620248B2
AU55107/90A
AU5510790A
AU620248B2
AU 620248 B2
AU620248 B2
AU 620248B2
AU 55107/90 A
AU55107/90 A
AU 55107/90A
AU 5510790 A
AU5510790 A
AU 5510790A
AU 620248 B2
AU620248 B2
AU 620248B2
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AU
Australia
Prior art keywords
catalyst
nickel
catalyst according
surface area
silicate
Prior art date
1989-05-16
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AU55107/90A
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AU5510790A
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Inventor
Cornelis Martinus Lok
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Uniqema BV

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Uniqema BV
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1989-05-16
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1990-05-16
Publication date
1992-02-13
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1990-05-16
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1990-11-22
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1992-02-13
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1992-02-13
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Classifications

C—CHEMISTRY; METALLURGY

C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES

C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM

C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom

C11C3/12—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by hydrogenation

C11C3/123—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by hydrogenation using catalysts based principally on nickel or derivates

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

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

B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium

B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof

B01J21/08—Silica

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

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

B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 – B01J23/36

B01J23/78—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 – B01J23/36 with alkali- or alkaline earth metals

C—CHEMISTRY; METALLURGY

C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES

C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES

C11B3/00—Refining fats or fatty oils

C11B3/02—Refining fats or fatty oils by chemical reaction

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

B01J35/002—Catalysts characterised by their physical properties

B01J35/0046—Physical properties of the active metal ingredient

B01J35/0053—Physical properties of the active metal ingredient 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

B01J35/02—Solids

B01J35/10—Solids characterised by their surface properties or porosity

B01J35/1033—Pore volume

B01J35/1038—Pore volume less than 0.5 ml/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

B01J35/02—Solids

B01J35/10—Solids characterised by their surface properties or porosity

B01J35/108—Pore distribution

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

B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts

B01J37/02—Impregnation, coating or precipitation

B01J37/03—Precipitation; Co-precipitation

B—PERFORMING OPERATIONS; TRANSPORTING

B82—NANOTECHNOLOGY

B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES

B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites

Abstract

The invention provides a nickel/silica catalyst optionally also containing cations of a lower Group II metal (X), which catalyst satisfies the following combination of features: 1) a molar ratio of SiO2/Ni = 0.15 = 0.35 2) a molar ratio of X/Ni = 0 – 0.15 3) an active nickel surface area above 120m<2>/g 4) a BET surface area of which at least 60% is found with pores with a radius below 1.5 nm. Preferably the catalyst has an atomic X/Ni ratio between 0.5 – 0.10 and a BET surface area of which at least 60% is found in pores having a pore radius of below 1.4 nm. The group II metal X is preferably magnesium or barium.

Description

a4 0 7 97 Z r; a i: 3i
AUSTRALIA
PATENTS ACT 1952 COMPLETE SPECIFICATION
(ORIGINAL)
FOR OFFICE USE 620248 Form Short Title: Int. Cl: Application Number: Lodged: *0 0 rt rc, c cc cc cc Complete Specification-Lodged: Accepted: Lapsed: Published: Priority: Related Art: TO BE COMPLETED BY APPLICANT cc r r r Si,’cc,, C I: r
CC
Cc o C 0, G0# a 4 r.
ccii oa CS.
O C Name of Applicant: Address of Applicant: Actual Inventor: Address for Service: UNICHEMA CHEMIE BV BUURTJE 1 2802 BE GOUDA THE NETHERLANDS GRIFFITH HACK CO., 601 St. Kilda Road, Melbourne, Victoria 3004, Australia.
«Sana-, Complete Specification for the invention entitled: NICKEL/SILICA CATALYST AND THE PREPARATION AND USE THEREOF.
The following statement is a full description of this invention including the best method of performing it known to me:- GRIFFITH HACK CO PATENT AN D TRADE MARK ATTORNEYS MELBOURNE SYDNEY PERTH r ;i 9; 0 0 0 0 o so 0 000 o 0 000900 0 0 o o0 0 0 0 oo a 0 0o 00 0 oo0 a 0 0 00 0 o 0 0 0 00 oo o 0 0 0 0400 O d nd 0 0 17- R7062 The invention relates to a nickel/silica catalyst which optionally comprise cations of a lower Group II metal to a process for the preparation of such a catalyst and to a hydrogenation process using this catalyst. More in particular the invention relates to a catalyst suitable for the hydrogenation of unsaturated organic compounds, especially fatty acids.
Nickel/silica catalysts which optionally comprise ions of another metal are known from the prior art and often they are obtained by coprecipitating methods in which the metal and silica are precipitated simultaneously from a metal salt/waterglass solution by means of an alkaline precipitating agent. Such a method is disclosed in DE-A-2631901 (NL Industries Inc).
EP-A-0031472 (Ruhrchemie) discloses a catalyst prepared by impregnating a porous silica and/or alumina material with metal salt solutions, sometimes with nickel and magnesium salt solutions, followed by filtering, drying, calcining and reduction. The catalyst is suitable for methanation processes.
1
I
i 2 R7062 European patent specification EP-A-322049 (Unilever), published 28 June 1989 describes the preparation and use of a nickel/silica catalyst which may comprise ions of a lower Group II metal This catalyst satisfies the following combination of features: o. 1) a molar ratio of SiO 2 /Ni 0.15 0.35 o ao 0 .00 o n 2) a molar ratio of X/Ni 0 0.15 0 2 o oo 3) an active nickel surface area above 120 m /g 0o a o oo o 0 0 0 0 0 4) a BET surface area of which at least 40% is found with pores with a radius above 2.5 nanometers, also this catalyst contains at least 50% of nickel.
0000 0 0 0oo. This catalyst, which has according to 4) mainly 00 fairly wide pores is very suitable for the selective hydrogenation of vegetable and animal oils and fats and 000 0 2 combines excellent activity and selectivity.
0 However, this latter catalyst and most other o catalysts are ideally not suitable for the hydrogenation o 0 of fatty acids and unsuitable for the hydrogenation of afeedstock of fatty acids containing 10 to 50 ppm of sulphur compounds (calculated as sulphur) such as e.g.
undistilled fatty acids of animal origin such as Sundistilled tallow fatty acids, undistilled soya bean fatty acids and undistilled rape seed fatty acids and so called «acid oils». When hydrogenating this type of feedstock at reasonable nickel levels the hydrogenation tends to stop when reaching an iodine values between and 50 due to poisoning of the catalyst.
3 R7062 The present invention provides a catalyst which is very suitable for the hydrogenation of fatty acids, especially those containing sulphur contaminants. This novel catalyst is characterized by the following combination of features: 1) a molar ratio of SiO 2 /Ni 0.15 0.40 0 00 0o.. 2) a molar ratio of X/Ni 0 0.15 o 0 2 0 10 3) an active nickel surface area above 120m /g nickel.
00 0 00 0 4) a BET surface area of which at least 55% is found with pores having a radius below 1.5 nanometers.
0ooo00 This catalyst has unusual narrow pores and when used 0 0 ooounder standard conditions of 0.4% of nickel shows a high oo 00 o activity leading in the case of standard soya bean fatty o o 2 acids to an end iodine value of below 2, often below 1.
ooo o Preferably the pores of the catalyst are so narrow o 0 that at least 60%, most preferably at least 65% of the BET surface area is found with pores having a radius below 000000 nanometers. This percentage of the surface in the pores, above or below a certain pore radius is a better yardstick for catalytic performance than a calculated average pore radius because such a figure ignores the distribution of pore radii. The percentage of the surface in pores above or below a certain pore radius can be determined together with catalyst surface area, pore volume by nitrogen adsorption techniques known as the extended Brunauer, Emmett and Teller (BET) method.
i; 4- R7062 Preferably the composition of the catalyst is such that the molar ratios X/Ni 0.05 0.10 and SiO 2 /Ni 0.20 0.30.
In another embodiment the lower Group II metal has an atomic number below 60, more preferably X is a Group IIa metal such as magnesium or barium, and the former is preferred.
ooo0 09 00 The present invention provides a catalyst in which 0 o 0 the active nickel surface area is above 120 m2/g of 0nickel. Also generally the catalyst according to the o 00 present invention has a pore volume of at most 0.35 ml/g, preferably at most 0.28 ml/g catalyst.
00000 As to catalytic performance the present novel catalysts are such that the standard soya bean fatty acid 0o 0 activity as defined below is such. that the end iodine O 00 value of standard undistilled fatty acids under standard 0 0 conditions is below 2, preferably below i.
0 Usually the catalyst according to the present o o insvention has an active nickel surface area of above 120, preferably above 130 m2/g. Also the catalyst according to the present invention contains as a rule at least preferably at least 65% of nickel. As to catalytic properties the catalyst according to the present invention normally shows an activity of the catalyst by hydrogenation of standard undistilled soya bean fatty acids under standard conditions as defined below leads to an end iodine value below 5, preferably below 1.
The catalyst according to the present invention can conveniently be prepared by continuously precipitating nickel ions from an aqueous salt solution, optionally LL -I r IL IL- 5 R7062 together with X-ions, with an excess alkaline precipitating agent in a stirred reactor with a residence time of between 20 and 120 seconds, followed by continuous addition of aqueous silicate solution, optionally in a second reactor, collecting, drying and reducing the S precipitate characterized in that the temperature of the suspension when adding the aqueous silicate solution is between 90 and 950C, for a period of between 10 and 300 a90 °o.o0 minutes preferably between 30 and 60 minutes.
0 0 :0 As a rule the reactor(s) contain a device for o 0 o vigorously agitating the liquid. After the second reactor o o othe suspended unreduced catalyst is separated, usually by filtration, but prior to that it is kept in a storage tank at an elevated temperature, preferably at a temperature 00000 between 75 and 950C where it is mildly stirred. Also o oo0000 there is the possibility of dosing the silicate to the 0000
I
0 0 o o suspension in more than one reactor, but the total average 0 residence time in this step should remain within the oo oindicated range. The precipitation of the catalyst can be carried out discontinuously (batchwise) or,continuously o0 by the cascade method). Stirring of the reactor(s) 0ooi 0is preferably carried out with an input of mechanical 000040 ooo 0 o energy of 5 2000 Watt per litre of solution.
Nickel compounds which can be used as starting material for the preparation of the catalyst according to the present invention are watersoluble nickel compounds such as nitrate, sulphate, acetate, chloride or formate.
The solution fed into the first reactor contains between and 80 grams of nickel per litre, particularly preferred are solutions containing between 25 and 60 g metal per litre. The Group II metal compound, in particular magnesium, is conveniently also used in the form of a watersoluble compound such as the nitrate or 1* L 6 R7062 chloride. Alkaline precipitation agents which may be used as starting material in the precipitation step are alkali metal hydroxides, alkali metal carbonates, alkali metal bicarbonates, the corresponding ammonium compounds and mixtures of these compounds. The concentration of the alkaline precipitation agent which is fed in stoichiometric excess into the first reactor is preferably o0 0 0 20 to 300 grams of alkaline material per litre (calculated n.
0 as dry material) as far as the solubility permits to do so, more particularly between 50 and 250 g per litre.
0 o 10 o 00 oo 0 0 00 Preferably precipitation of nickel ions and 00 a optionally X-ions with alkaline precipitation agent takes.
place at a temperature of between 20 and 95°C and the aqueous silicate is added at a reactor temperature between 0ooo 90 and 95 0 C. Ageing or maturing of the suspension in an 0ooo ageing or optionally filtering tank takes place at a 6o a temperature between 75 and 95 0 C, preferably between 80 and 20 90 0
C.
0 oo Suitable soluble silicates used in the preparation of S0 the catalysts according to the present invention are 0 0 0 alkali silicates, more especially sodium silicate and 0000o o0 0 neutral silicate such as Na20.3Si03 is preferred. The addition of soluble silicate should take place as quickly as possible after precipitation of the metal(s), preferably within 100 seconds.
The amounts and ratios of nickel, Group II metal, soluble silicate and alkaline precipitating agent added to the reactors depend on the desired composition of the eventual catalyst and can be easily calculated.
The catalysts according to the present invention may contain a water insoluble carrier material which was 1′ i 7 R7062 already present during the preparation or was added thereto later. Suitable carrier materials are e.g. silica containing materials like kieselguhr, aluminium trioxide (alumina) and silicates as bentonite. According to the present invention, however preferably no insoluble carrier is used. Nevertheless for special purposes the presence of an insoluble carrier can be desirable as a filter aid). If insoluble carrier material is used, this material can be added direct as such, as an aqueous I ooosuspension, preferably as a suspension in the aqueous 0 o o o0 solution of a metal salt, or as a suspension in the 0 0 a aqueous solution of the alkaline precipitating agent.
o o00 In a preferred embodiment, in which the precipitation of the metal ions is carried out continuously, the amounts 00 of solutions to be fed into the first reactor are dosed by determining, optionally continuously, the alkalinity 000 o00 o normality) of the discharged liquid. This can also be done by pH detirmination (pH 7- 10). The temperature at which °the precipitation of the metal(s) takes place can conveniently be controlled by adjusting the temperatures a0 of the solutions fed in. In any of the two or more o 000 reactors or the storage tank prior to filtration other 0 o0o compounds, if any, may be added such as a carrier material, some alkaline solution and/or possible promoters such as copper, zirconium, cobalt, molybdenum, silver, possibly other metals or combinations thereof so that their amount in the eventual catalyst does not exceed mole percent of the metal content.
After the silicate addition has been completed the solid components are separated from the mother liquor, washed with water if necessary, e.g. in the presence of a surface active material or organic solvent, e.g. acetone, 8 R7062 and subsequently dried by means of spray-drying, freeze-drying, or oven-drying.
Thereafter, if desired, the dry solid material is optionally ground and/or calcined and then activated 1 reduced) with hydrogen gas at an increased temperature, which as a rule lies between 30 0 and 450 0 C. The o* o o activation can take place at atmospheric or under reduced 0.0° pressure. The reduced catalyst so obtained is then usually .0 suspended in hydrogenated fatty material, often o 0 o o0 triglyceride oil or fatty acids.
o o 0 0 0 0..0 °Another embodiment of the invention provides a method for the hydrogenation of unsaturated organic compounds, in particular fatty acids, more especially those which are undistilled and contaminated with 10 to 50, more o °o particularly 20 30 ppm of sulphur compounds (calculated o00 as sulphur). These hydrogenations are carried out o o conveniently at an increased temperature (800 250 0 C) and 0 o 0 0 0 optionally increased pressure (1.0 to 5 MPa) with hydrogen. The amount of catalyst employed ranges between o 000 0.05 and 0.8 of nickel calculated on the fatty acids.
0000 Especially at pressures below 1.7 MPa performance was 0 0000 excellent.
The hydrogenated fatty material, especially fatty acids, so obtained show a favourable combination of properties such as low iodine value (below 3, most preferably below and have a good stability and a light colour.
The invention is illustrated by the following examples: i R7062 Example 1 Aqueous solutions of a) the nitrate salts of Ni and 2 3 Mg (0.6 M Ni and 0.06 M Mg) and b) Na2CO 3 (10 wt were continuously pumped at equal flow rates into a vigorously stirred precipitation reactor during which Ni and Mg Sooe precipitated forming a mixed Ni/Mg hydroxycarbonate. The oC o o o precipitation took place at a temperature of 500C and at a pH of 8.8. In the precipitation reactor the suspension had o o S0 an average residence time of 25 sec. The suspension was 0 O 0 0 continuously transferred into a second, stirred reactor o oo o a (energy input 4 Watt/litre) in which the average residence time was 30 minutes and the temperature was 92 0 C and a pH of 8.9. Simultaneously an amount of silicate ions were o dosed into this reactor continuously in the form of oa C waterglass Sio whilst maintaining the temperature.
oo° 0 The SiO 2 /Ni molar ratio was 0.21. The suspension o discharged by the second reactor was continuously fed into .o 20 a large filter storage tank from which the suspension was led to a filter where the precipitate was washed with water of 80°C to remove Na ions. The washed green filtercake was then dried in a spray dryer at 1200C.
0 Thereafter the green powder was reduced in a H 2 atmosphere for 30 minutes at a temperature of 430°C to give the active catalyst. The catalyst was characterized by the following chemical and physical methods: 1. The chemical composition expressed as a Sio 2 /Ni or (SiO 2 X)/Ni (molar ratio) was determined by X-ray fluorescence.
10 R7062 2. The active nickel surface area (expressed as m 2 /g nickel was determined by H 2 chemisorption after reduction of the green cake at 430 0
C.
3. The catalyst surface area, pore volume and the pore size (distribution) were determined by nitrogen adsorption (Brunauer, Emmett and Teller method, BET).
go To this end the green cake was reduced at 430 0 C and o0 the resulting pyrophoric catalyst was passivated in a o000oo o 1% 0 2
/N
2 gas mixture at 10 0
C.
0 a 10 0 0 0 o000 The results of the above determinations are given in 0 00 o0 o0 Table 1, where a comparison is made with two catalysts of identical composition but prepared at silicate addition temperatures of 96 and 980C. The catalytic activities of the catalyst were determined by hydrogenating standard a soya bean fatty acids with an S-content of 33 ppm, iodine 0000 o0 value of 126, acid value 200, saponification value 202, soap content 0.04% and water content 0.11%. The 0 00 O 90 0 hydrogenation was carried out at the following conditions: Catalyst dosage 0.45% (as Ni) 0 00 Do oa oo 0 Temperature 220 0
C
0 «a00 Pressure 1.5 MPa reaction time 2.0 hrs Catalytic performance is expressed as end iodine value.
f 1 R7062 Example 1 Comparison 1 Comparison 2 Temperature of 92 0 C 960C 98 0
C
silicate addition 0 oe End Iodine value 2.0 10.1 57.2 00 Si0 2 /Ni (molar) 0.21 0.21 0.20 o o o 00
I
Ni surface area m2/g 130 128 148 (Ni) 0000 ooo BET surface area 262 274 319 0° (m 2 /g) 0 00 000 20 Percentage of 63 40 28 catalyst surface in pores below 0.00 radius 0 0 The catalytic activity and selectivity of the catalyst were determined by hydrogenating two types of edible oil i.e. soybean oil and refined fish oil.
Example 2 The catalyst of Example 1 (silicate addition at 92 0
C)
was used in the hydrogenation of tallow fatty acids (containing 10 ppm of having an iodine value of 58.
The conditions were: I1L -YL_ I i ,1 -I :d 12 R7062 Catalyst dosage Temperature Pressure Reaction time 0.022% (as Ni) 2000C 1.4 MPa 3 hours 00 oo o o 0 000 0000 o o o o 0000 o 0000 0 000000 10 000 1 0 00 0 C 0 o000 0 The end iodine value was 1.0 (after 2 hrs A reference catalyst with wider pores 45% of the surface area in pores smaller than 1.5 nm yielded an end iodine value 22 (after 3 hrs).
Example 3 As Example 1, but nickel nitrate was replaced by nickel sulphate as raw material (same amount of Nickel) and a silicate dosing temperature of 94°C was applied. The resulting end iodine value in the soya bean fatty acid hydrogenation test was 2.4.
oooo 0000 0000 0 0 0 00 0 0 0 00 00 0 0000 0 0 noo.» g O o oo Example 4 As Example 1, but the silica/nickel ratio was raised to 0.24, the Mg/Ni ratio was 0.10 and the reduction temperature was lowered from 430 to 400 0 C. This resulted’ in a catalyst of the following features: Active nickel surface area 123 m2 /g (Ni) 2 BET-surface area 303 m /g catalyst pore volume 0.26 ml/g catalyst Percentage of surface area in pores smaller than nm is 68%. The end iodine value in the standard soya bean fatty acid hydrogenation test was f
J

Claims (14)

1. A nickel/silicate catalyst, characterized in that the reduced catalyst satisfies the following combination of features: 1) a molar ratio of Si0 2 /Ni 0.15 0.40 2) an active nickel surface area above 120 m 2 /g nickel 3) a BET surface area of which at least 55% is found with pores having a radius below 1.5 nanometers.

2. A nickel/silicate catalyst according to claim 1, characterized in that the catalyst contains cations of a lower Group II metal up to a molar ratio X/Ni of 0.15. 00 o car oo,» 3. A catalyst according to claim 2, characterized in that X/Ni 0.05 0.10. oo,, 0 cc 00: 4. A catalyst according to any of the preceding oo 15 claims, characterized in that the BET surface area is such that at least 60% is found with pores having a radius below nanometers. A catalyst according to any of the preceding claims, characterized in that the molar ratio of SiO 2 /Ni is 0.20 0.30.

6. A catalyst according to claim 2, characterized in that X is magnesium. O 7. A catalyst according to claim 2, characterized in that X is barium.

8. A catalyst according to any of the preceding pl^j claims, characterized in that the active nickel surface area is greater than 130 m 2 /nickel. 14

9. A catalyst according to any of the preceding claims, characterized in that the pore volume is at most 0.35 ml/g. ‘II .4. ii A catalyst according to claim 9, characterized in that the pore volume is at most 0.28 ml/g.

11. A catalyst according to any of the preceding claims, characterized in that the catalyst contains at least 50% of nickel.

12. A catalyst according to claim 11, characterized in that the catalyst contains at least 65% of nickel.

13. A catalyst according to any of the preceding claims, characterized in that the activity of the catalyst determined by hydrogenation of standard undistilled soya bean fatty acids under standard conditions as defined above leads to an end iodine value smaller than A catalyst according to claim 13, characterized in that the activity of the catalyst leads to an end iodine value smaller than 3. 00 O tt toot o 00 00 0 000 0 0 00. 00 0 000 0 0r 0 O (c 0 Cr 00a 0 000 40 0 0 C

15. A process for preparing a nickel/silica catalyst having a combination of features as claimed in claim 1 by continuously precipitating nickel ions from an aqueous salt solution with an excess alkaline precipitating agent in a stirred reactor with a residence time of between 20 and 120 seconds followed by continuous addition of aqueous silicate solution, collecting, drying and reducing the precipitate, characterized in that the temperature of the suspension when adding the aqueous silicate solution is between 90 and 0 C, for a period of between 10 and 300 minutes.

16. A process according to claim 15 for preparing a S ,4 nickel/silicate catalyst containing cations of a lower U Group II metal characterized in that nickel ions are :15 ;I f 15 precipitated together with X-ions from an aqueous solution.

17. A process according to claim 15 or 16, characterized in that the silicate solution is added in a second reactor.

18. A process according to claim 15 or 16, characterized in that the temperature of the suspension when adding the silicate solution is between 92 and 940C.

19. A process according to claim 15 or 16, characterized in that the temperature is kept for a period of between 30 and 60 minutes. A process according to claim 15 or 16, characterized in that at least one reactor is stirred with 00 an input of mechanical energy of 5 -2000 Watts per litre of 00 o* solution. 000oo0 0 0 0000 0.000 15 21. A process for the hydrogenation of unsaturated o organic compounds, characterized in that a catalyst 0oo 0 o oo according to claims 1 14 is used. 00 0

22. A process according to claim 21, characterized in that the unsaturated organic compound is a unsaturated 4000 20 fatty acid. 0 DATED THIS 25TH DAY OF NOVEMBER 1991 J UNICHEMA CHEMIE BV By its Patent Attorneys: GRIFFITH HACK CO. 25 Fellows Institute of Patent ,t Attorneys of Australia. C t ,r ii,

AU55107/90A
1989-05-16
1990-05-16
Nickel/silica catalyst and the preparation and use thereof

Ceased

AU620248B2
(en)

Applications Claiming Priority (2)

Application Number
Priority Date
Filing Date
Title

EP89201229

1989-05-16

NL89201229

1989-05-16

Publications (2)

Publication Number
Publication Date

AU5510790A

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Nickel/silica catalyst and the preparation and use thereof

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Families Citing this family (21)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

DD299623A5
(en)

1989-05-16
1992-04-30
��@��@�@��@��@��@��@�}��@�k��

NICKEL / SILICON CATALYST AND METHOD AND MANUFACTURE THEREOF

DE4025525A1
(en)

1990-08-11
1992-02-20
Hoechst Ag

CARRIER CATALYSTS AND A METHOD FOR THEIR PRODUCTION

DE4141771A1
(en)

1991-12-18
1993-06-24
Hoechst Ag

PROCESS FOR THE PREPARATION OF AMINES BY CATALYTIC HYDROGENATION OF NITRILES

CA2145094A1
(en)

1992-09-21
1994-03-31
Brigitte Feldhauser
Nickel/silica catalyst for hydrotreating unsaturated organic compounds

DE4310053A1
(en)

1993-03-27
1994-09-29
Hoechst Ag

Hydrogenation catalyst, a method of preparation and use

IT1268868B1
(en)

1993-06-16
1997-03-13
Mini Ricerca Scient Tecnolog

PROCEDURE FOR THE PREPARATION OF A METALLIC CATALYST WITH SITU GENERATED SUPPORT FOR THE HYDROGENATION OF ORGANIC COMPOUNDS AND

AU9471898A
(en)

1997-09-05
1999-03-29
Henkel Corporation
Method of making hydrogenated acids

US6391815B1
(en)

2000-01-18
2002-05-21
Süd-Chemie Inc.
Combination sulphur adsorbent and hydrogenation catalyst for edible oils

US7468342B2
(en)

2001-05-22
2008-12-23
Mitsubishi Gas Chemical Company, Inc.
Catalysts and process for producing aromatic amines

US20040063576A1
(en)

2002-09-30
2004-04-01
Sud-Chemie Inc.
Catalyst adsorbent for removal of sulfur compounds for fuel cells

US7585990B2
(en)

2003-07-31
2009-09-08
Cargill, Incorporated
Low trans-fatty acid fat compositions; low-temperature hydrogenation, e.g., of edible oils

WO2005012471A2
(en)

2003-07-31
2005-02-10
Cargill, Incorporated
Low trans-fatty acid fat compositions; low-temperature hydrogenation, e.g., of edible oils

GB0501783D0
(en)

2005-01-28
2005-03-09
Johnson Matthey Plc
Catalysts and preparation method

CA2601124C
(en)

2005-03-24
2013-12-17
Idemitsu Kosan Co., Ltd.
Desulfurizing agent and method of desulfurization with the same

JP5196734B2
(en)

2006-05-17
2013-05-15
Ｊｘ日鉱日石エネルギー株式会社

Hydrorefining method

US20080318766A1
(en)

2007-06-21
2008-12-25
Quaid-E-Azam University
Novel nanocatalyst for edible oil hydrogenation

JP5179107B2
(en)

2007-07-24
2013-04-10
花王株式会社

Catalyst for hydrogenation

CN101481315B
(en)

2008-11-07
2012-05-23
甘肃中科药源生物工程有限公司
Method for preparing X substituted diamino naphthalin from X substituted 1,4-dinitronaphthalene

EP2371937A1
(en)

2010-03-26
2011-10-05
BASF Corporation
Process for the hydrogenation of fatty acids using a promoted supported nickel catalyst

EP2380953A1
(en)

2010-04-22
2011-10-26
BASF Corporation
Hydrogenation of fatty acids using a promoted supported nickel catalyst

KR101655764B1
(en)

2014-12-31
2016-09-09
한경대학교 산학협력단
Nickel catalyst and Hydrogenated Castor oil produced by this Nickel catalyst

Citations (1)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US4666635A
(en)

1983-01-20
1987-05-19

Internationale Octrooi Maatschappij «Octropa» B.V.

Nickel-based catalyst, its preparation and its application

Family Cites Families (12)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

FR956586A
(en)

1942-02-05
1950-02-02

GB1195307A
(en)

1968-03-04
1970-06-17
Ici Ltd
Dimerisation of Olefines

LU57716A1
(en)

1968-12-30
1970-07-01

US3868332A
(en)

1970-10-26
1975-02-25
Exxon Research Engineering Co
Massive nickel catalysts

GB1367088A
(en)

1970-12-21
1974-09-18
Unilever Ltd
Catalysts

CA1078878A
(en)

1975-07-16
1980-06-03
Nl Industries
Process of catalytic methanation

DE2952683A1
(en)

1979-12-29
1981-07-02
Ruhrchemie Ag, 4200 Oberhausen

METHANIZATION CATALYST AND METHOD FOR PRODUCING IT

FR2502142B1
(en)

1981-03-17
1983-12-02
Inst Francais Du Petrole

DE3221076A1
(en)

1982-06-04
1983-12-08
Basf Ag, 6700 Ludwigshafen

METHOD FOR PRODUCING MEDICAL WHITE OILS BY CATALYTIC HYDRATION AND CATALYSTS THEREFOR

NL190602C
(en)

1983-12-06
1994-05-16
Unilever Nv

Process for preparing a nickel / nickel silicate catalyst and process for hydrogenating organic compounds therewith.

DE3880113T2
(en)

1987-12-21
1993-07-15
Unilever Nv

NICKEL SILICONE CATALYSTS AND THEIR PREPARATION.

DD299623A5
(en)

1989-05-16
1992-04-30
��@��@�@��@��@��@��@�}��@�k��

NICKEL / SILICON CATALYST AND METHOD AND MANUFACTURE THEREOF

1990

1990-05-15
DD
DD90340688A
patent/DD299623A5/en
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1990-05-15
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KR1019900006978A
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IP Right Cessation

1990-05-16
US
US07/524,262
patent/US5112792A/en
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Expired – Lifetime

1990-05-16
AT
AT90305252T
patent/ATE85765T1/en
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IP Right Cessation

1990-05-16
AU
AU55107/90A
patent/AU620248B2/en
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1990-05-16
EP
EP90305252A
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Expired – Lifetime

1990-05-16
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1990-05-16
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DE9090305252T
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Expired – Lifetime

1990-05-16
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IN123BO1990
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1990-05-16
JP
JP2124318A
patent/JPH0628732B2/en
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Expired – Fee Related

1990-05-16
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BR909002294A
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IP Right Cessation

1990-05-16
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DK90305252.0T
patent/DK0398668T3/en
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1990-05-16
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not_active
Expired – Lifetime

1991

1991-07-24
IN
IN217/BOM/91A
patent/IN171890B/en
unknown

1994

1994-07-06
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US08/268,545
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Patent Citations (1)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
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Title

US4666635A
(en)

1983-01-20
1987-05-19
Internationale Octrooi Maatschappij «Octropa» B.V.
Nickel-based catalyst, its preparation and its application

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ATE85765T1
(en)

1993-03-15

IN171000B
(en)

1992-06-27

KR930008440B1
(en)

1993-09-04

EP0398668A1
(en)

1990-11-22

IN171890B
(en)

1993-01-30

JPH03207449A
(en)

1991-09-10

US5112792A
(en)

1992-05-12

JPH0628732B2
(en)

1994-04-20

AU5510790A
(en)

1990-11-22

CA2016817C
(en)

1998-06-23

US5463096A
(en)

1995-10-31

ES2040051T3
(en)

1993-10-01

EP0398668B1
(en)

1993-02-17

DD299623A5
(en)

1992-04-30

CA2016817A1
(en)

1990-11-16

BR9002294A
(en)

1991-08-13

KR900017659A
(en)

1990-12-19

DK0398668T3
(en)

1993-05-10

ZA903747B
(en)

1992-02-26

DE69000925D1
(en)

1993-03-25

DE69000925T2
(en)

1993-07-08

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