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CA2510258A1 - Process for the preparation of catalyst microspheres - Google Patents

Process for the preparation of catalyst microspheres Download PDF

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Publication number
CA2510258A1
CA2510258A1 CA002510258A CA2510258A CA2510258A1 CA 2510258 A1 CA2510258 A1 CA 2510258A1 CA 002510258 A CA002510258 A CA 002510258A CA 2510258 A CA2510258 A CA 2510258A CA 2510258 A1 CA2510258 A1 CA 2510258A1
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CA
Canada
Prior art keywords
catalyst
particles
ingredients
process according
catalyst ingredients
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
CA002510258A
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French (fr)
Inventor
Monique Van Der Zon
Erik Jeroen Laheij
Paul O'connor
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Albemarle Netherlands BV
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Individual
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Filing date
Publication date
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Publication of CA2510258A1 publication Critical patent/CA2510258A1/en
Abandoned legal-status Critical Current

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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
    • 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
    • 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
    • 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
    • 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
    • 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

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Catalysts (AREA)
  • Glanulating (AREA)

Abstract

The present invention relates to a process for the preparation of catalyst particles with a particle diameter in the range 20-2000 microns involving th e steps of agitating at least two dry catalyst ingredients, spraying a liquid binding agent on the catalyst ingredients while continuing the agitation, an d isolating formed catalyst particles with the desired particle diameter and comprising the catalyst ingredients. In contrast to the conventional way of preparing such particles, spray-drying, the present process allows the formation of small particles from slurries with a high solids content. Hence , smaller amounts of liquid have to be evaporated, which makes the process energy efficient.

Description

PROCESS FOR THE PREPARATION OF CATALYST MICROSPHERES
The present invention relates to a process for the preparation of catalyst compositions with a particle diameter in the range 20-2000 microns.
Within the specification, the term catalyst compositions also encompasses catalyst additives and adsorbents.
For several catalytic applications, such as fluidized bed processes, small catalyst particles are required. Such particles are generally produced by spray-drying a mixture of the catalyst ingredients. For instance, fluid catalytic cracking (FCC) catalysts are generally prepared by spray-drying an aqueous slurry of zeolite, clay, and silica and/or alumina.
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.
Depending on the type of nozzle used, 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.
Unfortunately, only slurries with a low solids content (i.e. below about 45 wt%
solids) and, consequently, a high liquid content can be spray-dried. Slurries with a higher solids content either are too viscous to be pumped through the nozzle or will not give suitable droplets upon spraying.
Due to this low solids limitation, large volumes of liquid are required, which have to be evaporated during the drying step. This is energy inefficient.
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 ~, more preferably from 250 to 2500 s ~, and most preferably from 500 to 1000 s ~.
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, (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
5, 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.
Examples of suitable anionic clays (also called hydrotalcite-like materials or layered double hydroxides) are 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. The term "dry" in this context means that not more than 90% of the pore volume of these ingredients is filled with water.
Most of the 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-s exchange with NH4 and rare earth metals (RE), drying, calcination, and milling.
Suitable liquid binding agents include water, acidic aqueous solutions, or aqueous silicon andlor 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. For example:
If 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.
If 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. Alternatively, 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. Consequently, if one of the catalyst ingredients is an alumina and ACH
or ANH is used as liquid binding agent, 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).
If 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. Examples of 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 5 catalyst ingredients sequentially. For instance, a silicon-containing solution or sol, or an aluminium chlorohydrol or pitrohydrof-containing sol can be used as a first liquid binding agent, while acidified water can be used as a second liquid binding agent.
Depending on the extent of dryness of the catalyst ingredients, it 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 p,m.
Agitation is continued until the right particle size is obtained. In the case of fluidized bed granulation, 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. For fluid catalytic cracking (FCC) applications a particle size between 30 and 100 microns is preferred.
If desired, the resulting particles are dried andlor 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.
EXAMPLES
Example 1 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 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.
Example 3 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.

Claims (7)

8
1. Process for the preparation of catalyst particles with a particle diameter in the range 20-2000 microns, which process comprises the steps of:
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.
2. Process according to claim 1 wherein agitation is performed by high-shear mixing.
3. Process according to claim 1 wherein agitation is performed by fluidization.
4. Process according to any one of the preceding claims wherein at least one of the catalyst ingredients is alumina, clay, or zeolite.
5. Process according to claim 4 wherein the catalyst particles are FCC
catalyst particles or FCC catalyst additive particles.
6. Process according to any one of the preceding claims wherein the liquid binding agent is selected from the group consisting of water, an aqueous acidic solution, a silicon-containing solution or suspension, a suspension comprising aluminium chlorohydrol and/or aluminium nitrohydrol, and mixtures thereof.
7. Process according to claim 2 wherein the shear rate applied on the catalyst ingredients during high-shear mixing ranges from 250 to 1000 s-1.
CA002510258A 2002-12-18 2003-12-09 Process for the preparation of catalyst microspheres Abandoned CA2510258A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP02080617.0 2002-12-18
EP02080617 2002-12-18
PCT/EP2003/014169 WO2004054713A1 (en) 2002-12-18 2003-12-09 Process for the preparation of catalyst microspheres

Publications (1)

Publication Number Publication Date
CA2510258A1 true CA2510258A1 (en) 2004-07-01

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CA002510258A Abandoned CA2510258A1 (en) 2002-12-18 2003-12-09 Process for the preparation of catalyst microspheres

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EP (1) EP1572361A1 (en)
JP (1) JP2006510474A (en)
KR (1) KR20050085754A (en)
CN (1) CN1326618C (en)
AU (1) AU2003294844A1 (en)
BR (1) BR0317345A (en)
CA (1) CA2510258A1 (en)
SA (1) SA04250020B1 (en)
TW (1) TW200502039A (en)
WO (1) WO2004054713A1 (en)

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Publication number Priority date Publication date Assignee Title
JP5255844B2 (en) * 2004-12-21 2013-08-07 アルベマール・ネーザーランズ・ベー・ブイ Catalysts, methods for their production and uses thereof
JP4859774B2 (en) * 2007-07-17 2012-01-25 日揮触媒化成株式会社 Method for producing fluid catalytic cracking catalyst
EP2981603A1 (en) 2013-04-05 2016-02-10 D'Alcante B.V. Improved process for reducing the alcohol and/or sugar content of a beverage
CN103736489B (en) * 2013-12-24 2015-10-28 天津众智科技有限公司 The preparation method of preparing butadiene with butylene oxo-dehydrogenation fluid catalyst
GB201504072D0 (en) * 2015-03-10 2015-04-22 Metalysis Ltd Method of producing metal
BR112020010409B1 (en) 2017-11-28 2023-03-21 Blue Tree Technologies Ltd METHODS AND SYSTEMS TO PRODUCE BEVERAGES WITH LOW SUGAR CONTENT
WO2020012351A1 (en) * 2018-07-10 2020-01-16 Reliance Industries Limited Regenerative adsorbent composition for removal of chlorides from hydrocarbon and a process for its preparation
CN116212937B (en) * 2023-03-06 2024-09-13 青岛惠城环保科技集团股份有限公司 Preparation method of catalytic cracking catalyst for producing diesel oil in large quantity

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EP0163836B1 (en) * 1984-04-07 1988-10-12 Bayer Ag Process and apparatus for the production of granules
US4737478A (en) * 1986-07-02 1988-04-12 Chevron Research Company Process for the manufacture of spheroidal bodies by selective agglomeration
US5286370A (en) * 1987-12-28 1994-02-15 Mobil Oil Corporation Catalytic cracking using a layered cracking catalyst
US5001096A (en) * 1987-12-28 1991-03-19 Mobil Oil Corporation Metal passivating agents
CA1329580C (en) * 1987-12-28 1994-05-17 Pochen Chu Catalytic cracking catalysts for metals laden feeds
US5254516A (en) * 1992-03-26 1993-10-19 Research Triangle Institute Fluidizable zinc titanate materials with high chemical reactivity and attrition resistance
JP4266406B2 (en) * 1998-05-11 2009-05-20 日本ケッチェン株式会社 Granular catalyst carrier, catalyst using the carrier, and method for hydrotreating hydrocarbon oil using the catalyst
WO2002072474A1 (en) * 2001-02-09 2002-09-19 Akzo Nobel N.V. In situ formed anionic clay-containing bodies
EP1264635A1 (en) * 2001-06-05 2002-12-11 Akzo Nobel N.V. Process for the production of catalysts with improved accessibility

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Publication number Publication date
TW200502039A (en) 2005-01-16
BR0317345A (en) 2005-11-08
CN1726083A (en) 2006-01-25
EP1572361A1 (en) 2005-09-14
KR20050085754A (en) 2005-08-29
AU2003294844A1 (en) 2004-07-09
WO2004054713A1 (en) 2004-07-01
CN1326618C (en) 2007-07-18
SA04250020B1 (en) 2008-06-09
JP2006510474A (en) 2006-03-30

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