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
  • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
• • 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
  • B01J37/0009—Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
  • B01J37/0063—Granulating
• • 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
  • B01J29/00—Catalysts comprising molecular sieves
  • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
• • 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
  • B01J29/00—Catalysts comprising molecular sieves
  • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
  • B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
• • 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
  • B01J29/00—Catalysts comprising molecular sieves
  • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
  • B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
  • B01J29/08—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the faujasite type, e.g. type X or Y
  • B01J29/084—Y-type faujasite
• • 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
  • B01J37/04—Mixing
• • 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
  • B01J37/08—Heat treatment
• • 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
  • B01J2229/00—Aspects of molecular sieve catalysts not covered by B01J29/00
  • B01J2229/30—After treatment, characterised by the means used
  • B01J2229/42—Addition of matrix or binder particles
• • 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
  • B01J35/40—Catalysts, in general, characterised by their form or physical properties characterised by dimensions, e.g. grain size

Definitions

• the present invention relates to a process for the preparation of catalyst compositions with a particle diameter in the range 20-2000 microns.
• catalyst compositions also encompasses catalyst additives and adsorbents.
• FCC fluid catalytic cracking
• Spray-drying involves pumping a slurry containing the catalyst ingredients through a nozzle (a high-pressure nozzle or a rotating wheel with nozzle) into a chamber heated with hot air. During this process, high shear is placed on the slurry, thereby creating small droplets that quickly dry in the heated chamber.
• nozzle a high-pressure nozzle or a rotating wheel with nozzle
• the particle size distribution of the resulting catalyst particles depends on either the nozzle pressure or the rotating speed of the wheel, but generally lies in the range of 30-90 microns.
• This problem is solved by the process according to the present invention, which involves the following steps: a) agitating at least two dry catalyst ingredients, b) spraying a liquid binding agent on the catalyst ingredients while continuing the agitation, c) isolating formed catalyst particles with the desired particle diameter and comprising the catalyst ingredients, and d) optionally calcining the isolated catalyst particles.
• This process requires less liquid than spray-drying. Hence, less liquid has to be evaporated in the drying step, making this process more energy efficient than spray-drying.
• the process according to the invention requires at least two individual catalyst ingredients to form a catalyst particle. It is not a process that involves only surface coating of existing catalyst particles as in US 5,286,370 and US 5,001 ,096.
• Suitable agitation techniques involve fluidization and high-shear mixing.
• Fluidization is performed by fluidizing the catalyst ingredients in a stream of gas, generally air.
• a nozzle is present above the so formed fluidized bed. Through this nozzle, the liquid binding agent is sprayed on the catalyst ingredients.
• a suitable apparatus for performing this process is a fluidized bed granulator.
• the gas velocity influences the size of the catalyst particles obtained. This gas velocity preferably ranges from 1-10 times the minimum fluidization velocity and most preferably from 1-5 times the minimum fluidization velocity, with the minimum fluidization velocity being defined as the minimum gas velocity required for holding up the catalyst ingredients. It will be clear that this minimum velocity depends on the particle size of the catalyst ingredients: the larger the particles, the higher the required minimum gas velocity. Catalyst ingredients for the preparation of FCC catalyst particles generally have a particle size up to about 10 microns.
• the temperature of the gas preferably ranges from 20° to 700°C, more preferably from 50° to 200°C, and most preferably from 80° to 120°C.
• High-shear mixing is performed in a high-shear mixer.
• a nozzle is present in the mixer, above the catalyst ingredients. Through this nozzle, the liquid binding agent is sprayed on the catalyst ingredients.
• the preferred shear rate ranges from 250 to 5000 s "1 , more preferably from 250 to 2500 s “1 , and most preferably from 500 to 1000 s "1 .
• the temperature during high shear mixing preferably is below 100°C, more preferably below 50°C, and most preferably ambient.
• Catalyst ingredients which can be used in the process according to the invention include solid acids, alumina, iron (hydr)oxide, (meta)kaolin, bentonite,
• anionic clays (calcined) anionic clays, saponite, sepiolite, smectite, montmorillonite, and mixtures thereof.
• Suitable solid acids include zeolites such as zeolite beta, MCM-22, MCM-36, mordenite, faujasite zeolites such as X-zeolites and Y-zeolites (including H-Y- zeolites, RE-Y zeolites, and USY-zeolites), pentasil-type zeolites such as ZSM-
• non-zeolitic solid acids such as silica-alumina, sulphated oxides such as sulphated oxides of zirconium, titanium, or tin, sulphated mixed oxides of zirconium, molybdenum, tungsten, etc., and chlorinated aluminium oxides.
• Suitable aluminas include boehmite, pseudoboehmite, transition aluminas such as alpha-, delta-, gamma-, eta-, theta-, and chi-alumina, aluminium trihydrate such as gibbsite or bauxite ore concentrate (BOC), and flash-calcined aluminium trihydrate.
• anionic clays also called hydrotalcite-like materials or layered double hydroxides
• Mg-AI anionic clays Fe-AI anionic clays, Zn-AI anionic clays, Fe-Fe anionic clays, etc.
• the catalyst ingredients used have to be dry before starting the process according to the invention.
• dry in this context means that not more than 90% of the pore volume of these ingredients is filled with water.
• aluminas used for FCC applications are made via precipitation processes. These processes usually involve the sequential steps of precipitation, crystallization, and dewatering.
• a suitable dewatering technique to obtain alumina sufficiently dry to be used in the process according to the invention uses a high-pressure filter.
• Zeolites are usually prepared via crystallization, washing/dewatering, ion- exchange with NH 4 and rare earth metals (RE), drying, calcination, and milling.
• RE rare earth metals
• Suitable liquid binding agents include water, acidic aqueous solutions, or aqueous silicon and/or aluminium-containing solutions or suspensions.
• the term "liquid binding agent” refers to liquids, solutions, or suspensions that assist in binding of the catalyst ingredients to form the catalyst particles.
• the liquid binding agent can initiate this binding either during step b) or later, for instance during an additional calcination step. Whether or not binding takes place during step b) depends on the liquid binding agent and the catalyst ingredients used.
• the desired liquid binding agent depends on the desired binder.
• anionic clay is the desired binder
• water can be used as the liquid binding agent and a calcined anionic clay as one of the catalyst ingredients. Said water will rehydrate the calcined anionic clay to form a binder anionic clay.
• alumina is the desired binder
• acidified water can be used as liquid binding agent and a peptizable alumina such as pseudoboehmite as one of the catalyst ingredients.
• aluminium chlorohydrol (ACH) or aluminium nitrohydrol (ANH)-containing suspensions can be used as liquid binding agent, with formation of alumina binder, irrespective of the types of catalyst ingredients used.
• the resulting catalyst will comprise two types of alumina.
• Another option to obtain a catalyst particle with an alumina binder is to use water as the liquid binding agent and flash-calcined aluminium trihydrate as one of the catalyst ingredients. Although the latter combination does not result in binding of the particles during step b), binding does take place during an additional calcination step (step d).
• silica is the desired binder
• a solution or suspension containing a silicon compound can be used as liquid binding agent, irrespective of the types of catalyst ingredients used.
• suitable silicon compounds are silica sol, sodium (meta) silicate, and precipitated silica.
• More than one liquid binding agent can be used, which can be sprayed on the catalyst ingredients sequentially.
• a silicon-containing solution or sol, or an aluminium chlorohydrol or nitrohydrol-containing sol can be used as a first liquid binding agent, while acidified water can be used as a second liquid binding agent.
• the catalyst ingredients may be preferred to spray some water on the catalyst ingredients before spraying the liquid binding agent.
• the required amount of water is such that about 90% of the pores of the catalyst ingredients can be filled with water.
• the liquid binding agent is preferably sprayed on the catalyst ingredients at a rate of 1-1.5 times the required amount divided by the residence time. This residence time generally ranges from about 1 to 30 minutes.
• the droplet size preferably is between 1 and 20 ⁇ m.
• the gas velocity is selected in such a way that it can only hold up particles smaller than the desired size. Hence, once the particles have the desired size, they fall down.
• the particles obtained by the process according to the invention range in size from about 20 to about 2000 microns, preferably 20-600 microns, more preferably 20-200 microns, and most preferably 30-100 microns.
• FCC fluid catalytic cracking
• a particle size between 30 and 100 microns is preferred.
• the resulting particles are dried and/or calcined. If the applied liquid binding agent does not result in binding during agitation step b), a calcination step d) may be required to initiate this binding.
• Drying involves heating of the formed particles at a temperature preferably in the range 100-200°C. Calcination is preferably conducted at 300°-1200°C, more preferably 300°-800°C, and most preferably 300°-600°C for 15 minutes to 24 hours, preferably 1-12 hours, and most preferably 2-6 hours.
• the particles obtained by the process according to the invention can be used for various purposes, e.g. as a catalyst, adsorbent, etc.
• Suitable catalytic applications include Gas to Liquid processes (e.g. Fischer-Tropsch), E-bed and H-oil processes, reforming, isomerization, alkylation, and auto exhaust catalysis.
• This Example describes the preparation of FCC catalyst particles with the following composition (on dry base): 15 wt% alumina, 20 wt% USY, 4 wt% silica, 61 wt% kaolin.
• a fluidized bed granulator was filled with about 200 g of a mixture of dry pseudoboehmite, dry kaolin, and dry zeolite. The mixture was fluidized and afterwards 35 g of silicasol were sprayed on top of the fluidized bed at a rate of 4.8 g/min. Simultaneously, the inlet temperature of the gas was set to 70°C. Next, 10% nitric acid solution was sprayed on top of the fluidized bed through the same nozzle at a rate of 4.8 g/min. After addition of 100 g of the nitric acid solution, liquid addition was stopped and the gas inlet temperature was set to 135°C to dry the material. The resulting FCC particles had a mean diameter (d50) of 76 microns. SEM analysis showed that the particles had a uniform distribution of ingredients.
• Example 2 A fluidized bed granulator was filled with about 200 g of a mixture of dry pseudoboehmite, dry kaolin, and dry zeo
• This Example describes the preparation of FCC catalyst particles with the following composition (on dry base): 15 wt% pseudoboehmite, 20 wt% USY, 10 wt% alumina originating from aluminium chlorohydrol (ACH), 55 wt% kaolin.
• a fluidized bed granulator was filled with about 200 g of a mixture of dry pseudoboehmite, dry kaolin, and dry zeolite. The mixture was fluidized and afterwards 90 g of an aluminium chlorohydol suspension were sprayed on top of the fluidized bed at a rate of 4.8 g/min. Simultaneously, the inlet temperature of the gas was set to 70°C. Next, a 10% nitric acid solution was sprayed on top of the fluidized bed through the same nozzle at a rate of 4.8 g/min. After addition of 100 g of the nitric acid solution, the liquid addition was stopped and the gas inlet temperature was set to 135°C to dry the material. The resulting FCC particles had a mean diameter (d50) of 78 microns. SEM analysis showed that the particles had a uniform distribution of ingredients.
• This Example describes the preparation of FCC catalyst particles with the following composition (on dry base): 25 wt% pseudoboehmite, 25 wt% USY, 35 wt% kaolin, and 15 wt% Mg-AI anionic clay.
• a Mg-AI anionic clay was first calcined and then rehydrated in aquesous suspension at hydrothermal conditions, i.e. 130°C and autogeneous pressure.
• a fluidized bed granulator was filled with about 200 g of a mixture of dry pseudoboehmite, kaolin, the anionic clay, and zeolite. The mixture was fluidized and afterwards 10% nitric acid solution was sprayed on top of the fluidized bed through the same nozzle at a rate of 4.8 g/min. Simultaneously, the inlet temperature of the gas was set to 70°C. After addition of 100 g of the nitric acid solution, liquid addition was stopped and the gas inlet temperature was set to 135°C to dry the material.
• the resulting FCC particles have a mean diameter (d50) of 75 microns. SEM analysis showed that the particles had a uniform distribution of ingredients.

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• 2003
  • 2003-12-09 KR KR1020057011307A patent/KR20050085754A/ko not_active Application Discontinuation
  • 2003-12-09 WO PCT/EP2003/014169 patent/WO2004054713A1/en active Application Filing
  • 2003-12-09 AU AU2003294844A patent/AU2003294844A1/en not_active Abandoned
  • 2003-12-09 CA CA002510258A patent/CA2510258A1/en not_active Abandoned
  • 2003-12-09 JP JP2004560394A patent/JP2006510474A/ja active Pending
  • 2003-12-09 CN CNB2003801065323A patent/CN1326618C/zh not_active Expired - Fee Related
  • 2003-12-09 EP EP03785808A patent/EP1572361A1/en not_active Withdrawn
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