E-Book, Englisch, 150 Seiten
Worstell Adiabatic Fixed-Bed Reactors
1. Auflage 2014
ISBN: 978-0-12-801466-0
Verlag: Elsevier Science & Techn.
Format: EPUB
Kopierschutz: 6 - ePub Watermark
Practical Guides in Chemical Engineering
E-Book, Englisch, 150 Seiten
ISBN: 978-0-12-801466-0
Verlag: Elsevier Science & Techn.
Format: EPUB
Kopierschutz: 6 - ePub Watermark
Jonathan Worstell earned his Physics degree from Northwestern University then switched to the chemical sciences, earning an MS in Chemistry from Ball State University and a PhD in Applied Chemistry from Colorado School of Mines. Dr. Worstell worked at Eli Lilly and Company and Northwestern University Medical School prior to starting a thirty year career in the petrochemical industry. After retiring from the petrochemical industry, he began an academic career at University of Houston where he teaches senior level chemical engineering courses. Dr. Worstell also consults with several global petrochemical companies.
Autoren/Hrsg.
Weitere Infos & Material
1;Front Cover;1
2;Adiabatic Fixed-Bed Reactors;4
3;Copyright Page;5
4;Dedication;6
5;Contents;8
6;1 Introduction;10
6.1;1.1 Slow Reactions and Catalysts;10
6.2;1.2 Fixed-Bed Reactor Classification;13
6.3;1.3 Processes Operating Fixed-Bed Reactors;14
6.3.1;1.3.1 Ammonia Synthesis;14
6.3.2;1.3.2 Oxidation of Ethylene;16
6.3.3;1.3.3 Catalytic Reforming;17
6.3.4;1.3.4 Steam Methane Reforming;18
6.3.5;1.3.5 Double-Bond Isomerization/Metathesis/Hydrogenation;19
6.4;1.4 Operation of Fixed-Bed Reactors;20
6.5;1.5 Summary;20
6.6;References;21
7;2 Fundamentals of Fixed-Bed Reactors;22
7.1;2.1 Analysis of Fixed-Bed Reactors;22
7.2;2.2 Impact of Diffusion;28
7.3;2.3 Implication of Flow Regimes and Rate Controlling Mechanisms;31
7.4;2.4 Identification of Rate Controlling Regimes;33
7.5;2.5 Implications of Controlling Rate Regimes;38
7.6;2.6 Temperature Dependence of Controlling Regimes;40
7.7;2.7 Design of Fixed-Bed Reactors;41
7.8;2.8 Summary;41
7.9;References;41
8;3 Catalyst Deactivation;44
8.1;3.1 Introduction;44
8.2;3.2 Solid-Supported Catalyst Deactivation;45
8.3;3.3 Catalyst Deactivation by Chemical Mechanisms;45
8.4;3.4 Catalyst Deactivation by Thermal Mechanisms;49
8.5;3.5 Catalyst Deactivation by Mechanical Mechanisms;52
8.6;3.6 Solid Bases and Neutral Solids;53
8.7;3.7 Silica–Alumina Oxide Catalysts;54
8.8;3.8 Bifunctional Solid-Supported Catalysts;55
8.9;3.9 Reaction Schemes for Catalyst Deactivation;58
8.10;3.10 Catalyst Deactivation Parameter;61
8.11;3.11 Wave Front or Stream-Time Poisoning;65
8.12;3.12 Selectivity and Catalyst Deactivation;72
8.13;3.13 Summary;74
8.14;References;74
9;4 Improving Fixed-Bed Reactor Performance;76
9.1;4.1 Introduction;76
9.2;4.2 Improving Product Formation Rate;76
9.3;4.3 Improving Product Selectivity—Monofunctional Catalysts;82
9.4;4.4 Improving Product Selectivity—Bifunctional Catalysts;85
9.5;4.5 Summary;88
9.6;References;88
10;5 Scaling Fixed-Bed Reactors;90
10.1;5.1 Introduction;90
10.2;5.2 Models;91
10.3;5.3 Similarity;93
10.4;5.4 Theory of Models;97
10.5;5.5 Scaling Adiabatic Fixed-Bed Reactors;99
10.6;5.6 Scaling Pressure Drop Through a Catalyst Mass;108
10.7;5.7 Summary;117
10.8;References;117
11;6 Regeneration of Solid-Supported Catalysts;118
11.1;6.1 Introduction;118
11.2;6.2 To Regenerate or Not to Regenerate—That Is the Question;119
11.3;6.3 Regeneration of Coked Solid-Supported Catalyst;120
11.4;6.4 Summary;122
11.5;References;122
12;Appendix: Foundation of Dimensional Analysis;124
12.1;A.1 Introduction;124
12.2;A.2 Developing Dimensional Analysis;125
12.3;A.3 Foundation of Method of Indices;130
12.4;A.4 Dimensional Homogeneity;133
12.5;A.5 Matrix Formulation of Dimensional Analysis;135
12.6;A.6 Identifying Variables for Dimensional Analysis;139
12.7;A.7 Summary;140
12.8;References;141
Introduction
This chapter discusses the concept of catalysis and the reasons for designing, building, and operating fixed-bed reactors. It also presents the types of fixed-bed reactors available for use and relates reactor type to the heat transfer requirements of the chemical process. This discussion occurs via examples from the chemical processing industry. It also introduces the classification of fixed-bed reactors as adiabatic or nonadiabatic. This chapter also introduces the concepts of catalyst productivity and selectivity.
Keywords
Catalyst; fixed-bed reactor; adiabatic; nonadiabatic; catalyst productivity; selectivity
1.1 Slow Reactions and Catalysts
Many reactions are too slow to be commercially viable, no matter how much we desire the product. Over the centuries, we have learned that adding a particular chemical, such reactions proceed at commercially viable rates. We call that particular chemical a “catalyst.” A catalyst is a substance that accelerates a specific reaction toward its equilibrium but remains unchanged after the reaction achieves equilibrium.1 Many times the catalyst and product can be in the same phase at the end of the reaction. In other words, the catalyst contaminates the product and must be removed before the product is sold. Achieving this separation can be expensive, which increases the asking price for the product. Separation costs can actually make the product commercially unviable.
Two options exist for alleviating the problem of catalyst separation: (1) increase catalyst productivity to the point that only parts per million of it remain in the product and (2) make the catalyst stationary relative to product formation.
The first option may provide the simplest process, provided we can find a catalyst with sufficient productivity. Catalyst productivity is the rate at which reactant disappears or product appears
• per number of catalytic sites;
• per catalyst surface area;
• per catalyst volume or per catalyst weight.
The chemical processing industry (CPI) generally defines catalyst productivity as rate per unit catalyst weight.2
The chemical process could be as simple as charge the reactor with reactant, inject catalyst, stir, empty the reactor, then sell the product. While such a process certainly has its advantages, it also has some major disadvantages. First, since the catalyst remains in the product, its components must appear in the product specification, even if present as parts per million. If the product is a chemical intermediate, which means it undergoes further reaction, then any change in its specification must be communicated to its users and must gain their approval. In many cases, the processes using such chemical intermediates are sensitive to those parts per million of catalyst. In some cases, those parts per million are beneficial to the process; in most cases, they are a detriment to the process. Thus, the parts per million catalyst in the product must be controlled, which represents a manufacturing cost. A greater disadvantage is we cannot change the catalyst without informing our customers since we will have to alter the product specification. If we adopt a more cost-effective catalyst, our customers are going to want some or all of that cost savings, i.e., they will want a reduction in product price. Or—if those catalyst parts per million are beneficial to the customer, then the customer may simply refuse our request to change catalyst, thereby forcing us to supply current product for the life of the contract. But, the greater disadvantage of this option is the product tells the world what catalyst we used to manufacture product. Such insight allows them to use a similar catalyst or to develop a more productive catalyst.
Second, if the product enters the food chain, either as an ingestible or as a food container or wrapper, then it must undergo significant testing and costly certification by a variety of government agencies. Once a product gains regulatory approval, any change to its process or specification can represent recertification, which is a costly proposition. Thus, improving catalyst performance or changing the catalyst becomes problematic due to all the regulatory issues raised by such a change.
Third, what to do with product not meeting specification? This situation occurs when the catalyst is not as productive as it should be. In this case, the product contains too much catalyst. Diluting the “off-spec” material with “on-spec” product is the most likely action. Diluting in this fashion can require considerable time if the volume of off-spec material is large.
The second option is to immobilize the catalyst relative to process flow. In this case, the catalyst is stationary and the process fluid flows over it or through it. To immobilize a catalyst, we must adsorb, coprecipitate, or attach by some other means the active chemical component of the catalyst onto a solid. The solid must provide enough surface area to meet the productivity requirements of the process. In other words, the solid-supported catalyst must possess a productivity sufficient for economic viability. The solid must also possess enough strength to support its own weight when contained in a vessel. If these requirements are met, then we can install a fixed-bed reactor in our process.
There are several advantages to using a fixed-bed reactor in a catalyzed process. First, we know where the catalyst is—most of the time. Second, we do not have to recover the catalyst from any process stream or from our product. Third, product registration with a government agency may not be required, or, if required, will be simplified considerably since we do not leave trace amounts of catalyst in the product. This advantage can reduce the time to develop a given process and reduce development costs considerably since registration with a government agency may not be required. Fourth, we do not have to disclose the catalyst’s components in our product specification since the product does not contain them. This advantage allows us to decide whether to patent our catalyst or use it as a trade secret. Also, we do not have to inform customers of any catalyst change, unless so stipulated by the sales contract. Fifth, this option expands the choice of catalyst since the catalyst does not have to possess extraordinarily high catalytic productivity. Sixth, solid catalysts can be regenerated. Regeneration is a procedure that returns catalytic activity to or close to its original value. Regeneration generally involves burning organic chemical deposit off the catalyst’s solid surface, then chemically reducing the metal component of the catalyst before exposing it to process fluid.
Fixed-bed reactors also possess disadvantages. First, solid-supported catalytic productivity declines with time for a variety of reasons. In many cases, it is difficult to distinguish which mechanism is causing the catalytic deactivation. Thus, solid-supported catalysts require periodic regeneration or replacement. Second, solid-supported catalysts can move when the screens retaining the catalyst bed fail. When the retaining screens fail, catalyst flows into downstream piping and equipment. Such a screen failure initiates a massive maintenance effort to rehabilitate the process. Third, the solid-supported catalyst can be crushed by its own weight, thereby plugging the fixed-bed reactor. Fourth, the catalyst can attrite, i.e., form dust or fines, which escape the reactor and enter the downstream process. Such fines can blind filters, plug control valves, or accumulate in process dead-legs. In general, such fines cause havoc in the process.
When evaluating the advantages and disadvantages of fixed-bed reactors, the former generally overpowers the latter, making fixed-bed reactors the most popular method for catalyzing reactions in gas or liquid process streams.2(pp5–7)
1.2 Fixed-Bed Reactor Classification
We generally classify fixed-bed reactors as adiabatic or nonadiabatic. Adiabatic and nonadiabatic are thermodynamic terms describing energy exchange. Energy is an extensive variable, thus it depends upon the quantity of material being investigated. We call a given quantity of material a “system” and we idealize it as separated by real or imaginary walls from the rest of the universe, which we call the “surroundings.” By separating the system in this manner, we can control or observe energy exchange between it and its surroundings. A system may be isolated, in which case energy, either as heat or work, is not exchanged between the system and its surroundings. An adiabatic system exchanges work, but not heat, with its surroundings.3 Thus, the walls of an adiabatic system are heat opaque; they are insulated. But, systems with no or poor insulation can be adiabatic if any change within them occurs more rapidly than does achieving a new energy equilibrium with their surroundings, which is the case for fixed-bed reactors: localized events occur, then disappear, within fixed-bed reactors before a new energy equilibrium can be established with their surroundings.4 Adiabatic fixed-bed reactors are the reactor of choice for solid-supported catalysts due to their simple design, straightforward construction, and “hassle-free” operation.
Nonadiabatic fixed-bed reactors exist. They are used primarily in processes that are highly exothermic, such as oxidation of hydrocarbons. These reactors require heat transfer along the catalyst bed, which necessitates a high heat...




