Fundamental Principles of Drying
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1. Define: Unit Operation. Useful Physical Changes Occur in the Chemical Industry Is Known As a Unit Operation
INTREVIEW QUESTIONS 1. Define: Unit operation. Useful Physical changes occur in the chemical industry is known as a Unit Operation. Example: Distillation, Filtration, Drying, Extraction, Gas absorption, Crystallization, etc. 2. Define: Unit process. Useful Chemical changes with or without physical change occur in chemical industry are known as a Unit Process. Example: - Oxidation, Reduction, Alkylation, Sulfonation, Chlorination, etc. 3. Define: Boiling Point and Bubble Point. Boiling Point: -It is a temperature of a liquid at which the vapour pressure of the liquid is equal to atmospheric pressure. Bubble Point: -It is a temperature at which first bubble of vapour is formed. 4. When does liquid boil? When the vapour pressure of the liquid is equal to atmospheric pressure at that time liquid is boil. 5. Define: - Volatile Liquid. It is a tendency of a liquid to vaporize. 6. Acetone and water out of this which is more volatile and why? Acetone is more volatile than water because of boiling point of acetone (56.7 °C) is low compa re to boiling point of water (100° C) 7. What is the Relative Volatility? It is a ratio of concentration of more volatile component in vapour phase to liquid phase is called Relative Volatility 8. What is important of Relative Volatility? For separation of liquid mixture using distillation, Relative volatility should be more than 1. 9. Why is Reflux done in distillation column? and Define Reflux Ratio. For Increasing product purity. Reflux: -It is amount of distillate which is resend to distillation column is known as a reflux. Reflux Ratio: -Reflux ratio is the ratio of the portion of the overhead liquid product from a distillation column that is returned to the upper part of column to the portion of liquid collected as distillate. -
Evaluation of Azeotropic Dehydration for the Preservation of Shrimp. James Edward Rutledge Louisiana State University and Agricultural & Mechanical College
Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1969 Evaluation of Azeotropic Dehydration for the Preservation of Shrimp. James Edward Rutledge Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Rutledge, James Edward, "Evaluation of Azeotropic Dehydration for the Preservation of Shrimp." (1969). LSU Historical Dissertations and Theses. 1689. https://digitalcommons.lsu.edu/gradschool_disstheses/1689 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. This dissertation has been 70-9089 microfilmed exactly as received RUTLEDGE, James Edward, 1941- EVALUATION OF AZEOTROPIC DEHYDRATION FOR THE PRESERVATION OF SHRIMP. The Louisiana State University and Agricultural and Mechanical College, PhJD., 1969 Food Technology University Microfilms, Inc., Ann Arbor, Michigan Evaluation of Azeotropic Dehydration for the Preservation of Shrimp A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Food Science and Technology by James Edward Rutledge B.S., Texas A&M University, 1963 M.S., Texas A&M University, 1966 August, 1969 ACKNOWLEDGMENT The author wishes to express his sincere appreciation to his major professor, Dr, Fred H. Hoskins, for the guidance which he supplied not only in respect to this dissertation but also in regard to the author’s graduate career at Louisiana State University, Gratitude is also extended to Dr. -
Assessment of End-Of-Life Opportunities for Reverse Osmosis
Assessment of End-of-Life Opportunities for Reverse Osmosis Membranes Will Lawler A thesis in fulfilment of the requirements for the degree of Doctor of Philosophy School of Chemical Engineering Faculty of Engineering March 2015 i. Abstract Reverse osmosis (RO) membranes are now core to modern desalination processes and are widely used around the world. Based on the increasing number of desalination plants, and the finite lifespan of the membranes, the resulting number of used RO modules to be discarded is becoming a critical challenge. The overall aim of this study is to identify, develop and assess alternative end-of-life options for used RO elements and investigate the associated technical readiness, environmental impact, financial considerations and legislative challenges. The assessed end-of-life alternatives include, direct reuse of the old membranes within lower throughput systems; chemical conversion into porous, ultrafiltration (UF) like filters; direct reuse or recycling of the various module components; various energy recovery techniques, and landfill disposal. The results show that direct reuse is a promising application that can be utilised with minimal additional treatment or infrastructure; however, module storage techniques are a critical consideration, particularly as membrane drying has a significant and irreversible impact on membrane performance due to pore collapse in the polysulfone support layer. The method for chemical conversion with controlled exposure to NaOCl has been optimised, resulting in promising organic and virus removal properties, comparable to commercially available 10 – 30 kDa molecular weight cut off UF membranes; however, there was significant variation in hydraulic performance, ranging from 8 – 400 L.m-2.h-1.bar-1. -
Flash Column Chromatography Guide
8.9 - Flash Column Chromatography Guide Overview: Flash column chromatography is a quick and (usually) easy way to separate complex mixtures of compounds. We will be performing relatively large scale separations in 5.301, around 1.0 g of compound. Columns are often smaller in scale than this and some of you will experience these once you move into the research lab. Column chromatography uses the same principles discussed in the TLC Handout, but can be used on a preparative scale. We are running flash columns since we will use compressed air to push the solvent through the column. This not only helps provide better separation, but also cuts down the amount of time required to run a column. Reading: For an excellent description, see LLP pages 205 - 214. Preparing and Running a Flash Column: 1) Determine the dry, solvent-free weight of the mixture that you want to separate. 2) Determine the solvent system for the column by using TLC (see TLC Handout). You should aim for Rf values between 0.2 and 0.3. If your mixture is complicated then this may not be possible. In complex cases, you will probably have to resort to gradient elution. This simply means that you increase the polarity of the solvent running through the column (eluent) throughout the course of the purification. This technique will be described in more detail later in the handout, but for the TLC analysis you should determine which solvent systems put the different spots in the 0.2 to 0.3 Rf range. 3) Determine the method of application to the column. -
Settling-Thickening Tanks
Chapter 6 Settling-Thickening Tanks Pierre-Henri Dodane and Magalie Bassan Technology Learning Objectives • Understand in what contexts settling-thickening tanks are an appropriate treatment technology. • Understand the fundamental mechanisms of how settling-thickening tanks function. • Have an overiew of potential advantages and disadvantages of operating a settling-thickening tank. • Know the appropriate level of operations, maintenance and monitoring necessary to achieve solids-liquid separation in settling-thickening tanks. • Be able to design a settling-thickening tank to achieve the desired treatment goal. 6.1 INTRODUCTION Settling-thickening tanks are used to achieve separation of the liquid and solid fractions of faecal sludge (FS). They were fi rst developed for primary wastewater treatment, and for clarifi cation following secondary wastewater treatment, and it is the same mechanism for solids-liquid separation as that employed in septic tanks. Settling-thickening tanks for FS treatment are rectangular tanks, where FS is discharged into an inlet at the top of one side and the supernatant exits through an outlet situated at the opposite side, while settled solids are retained at the bottom of the tank, and scum fl oats on the surface (Figure 6.1). During the retention time, the heavier particles settle out and thicken at the bottom of the tank as a result of gravitational forces. Lighter particles, such as fats, oils and grease, fl oat to the top of the tank. As solids are collected at the bottom of the tank, the liquid supernatant is discharged through the outlet. Quiescent hydraulic fl ows are required, as the designed rates of settling, thickening and fl otation will not occur with turbulent fl ows. -
Stormwater Total Suspended Solids Removal Using a Coalescing Plate
Stormwater Total Suspended Solids Removal using a Coalescing Plate Separator Prepared for Jensen Precast and Mohr Separations Research, Inc. by Portland State University Table of Contents Abstract .....................................................................................................................2 Background ............................................................................................................... 2 Problem Statement and Objectives .......................................................................... 3 Experimental Testing Procedure .............................................................................. 4 Results .......................................................................................................................5 Conclusion ................................................................................................................ 9 References ............................................................................................................... 10 Appendix ................................................................................................................. 11 List of Figures Figure 1. Box plots for influent/effluent TSS concentrations ................................. 3 Figure 2. Photograph of setup ................................................................................. 4 Figure 3. Schematic drawing of setup ..................................................................... 4 Figure 4. Typical particle size distribution for U.S Silica -
MATERIAL BALANCE NOTES Revision 3 Irven Rinard Department
MATERIAL BALANCE NOTES Revision 3 Irven Rinard Department of Chemical Engineering City College of CUNY and Project ECSEL October 1999 © 1999 Irven Rinard CONTENTS INTRODUCTION 1 A. Types of Material Balance Problems B. Historical Perspective I. CONSERVATION OF MASS 5 A. Control Volumes B. Holdup or Inventory C. Material Balance Basis D. Material Balances II. PROCESSES 13 A. The Concept of a Process B. Basic Processing Functions C. Unit Operations D. Modes of Process Operations III. PROCESS MATERIAL BALANCES 21 A. The Stream Summary B. Equipment Characterization IV. STEADY-STATE PROCESS MODELING 29 A. Linear Input-Output Models B. Rigorous Models V. STEADY-STATE MATERIAL BALANCE CALCULATIONS 33 A. Sequential Modular B. Simultaneous C. Design Specifications D. Optimization E. Ad Hoc Methods VI. RECYCLE STREAMS AND TEAR SETS 37 A. The Node Incidence Matrix B. Enumeration of Tear Sets VII. SOLUTION OF LINEAR MATERIAL BALANCE MODELS 45 A. Use of Linear Equation Solvers B. Reduction to the Tear Set Variables C. Design Specifications i VIII. SEQUENTIAL MODULAR SOLUTION OF NONLINEAR 53 MATERIAL BALANCE MODELS A. Convergence by Direct Iteration B. Convergence Acceleration C. The Method of Wegstein IX. MIXING AND BLENDING PROBLEMS 61 A. Mixing B. Blending X. PLANT DATA ANALYSIS AND RECONCILIATION 67 A. Plant Data B. Data Reconciliation XI. THE ELEMENTS OF DYNAMIC PROCESS MODELING 75 A. Conservation of Mass for Dynamic Systems B. Surge and Mixing Tanks C. Gas Holders XII. PROCESS SIMULATORS 87 A. Steady State B. Dynamic BILIOGRAPHY 89 APPENDICES A. Reaction Stoichiometry 91 B. Evaluation of Equipment Model Parameters 93 C. Complex Equipment Models 96 D. -
SEPARATION PROCESS DRYING Part 1
SEPARATION PROCESS DRYING Part 1 by Zulkifly bin Jemaat Faculty of Chemical and Natural Resources Engineering email: [email protected] Introduction • Drying – removal of relatively small amounts of water (or organic liquid) from material – water is removed as a vapor by air • Evaporation – removal of relatively large amounts of water from material – water is removed as vapor at its boiling point • Water also can be removed mechanically from solid materials by means of presses, centrifuging and other methods • Drying is usually the final processing step before packaging and makes many material more suitable for handling (i.e. soap powder, dye, etc.) • Drying or dehydration of biological materials (especially food) is used as a preservation techniques. • Microorganisms are not active when the water content is less than 10%, normally foods are dried less than 5% water content to preserve flavor and nutrition. • Freeze-dried for biological & pharmaceuticals materials which may not be heated for ordinary drying 2 Methods of Drying • Based on operation – Batch - material is inserted into the drying equipment and drying proceeds for given period of time. – Continuous - material is continuously added to the dryer and dried material continuously removed. • Based on physical conditions used to add heat or remove water vapor – Direct contact with heated air at atmospheric pressure, and water vapor formed is removed by the air. – Vacuum drying – evaporation is enhanced by lowering the pressure over the wet material and heat may be added by direct contact with a metal tray holding the wet material or by radiation (IR). – Freeze drying – Low pressures and temperatures are employed to cause the water to sublime from a solid state (ice). -
Unit Operations for Bioprocess Engineers
Unit Operations for Bioprocess Engineers Chenming (Mike) Zhang Department of Biological Systems Engineering Virginia Polytechnic Institute and State University Blacksburg, VA 24061 Abstract Unit Operations in Biological Systems Engineering was introduced into the curriculum at Virginia Tech in 2000. It is a lecture and laboratory combined course. The lectures and experiments covered in the course had a narrow focus before the author took over in 2002. To broaden the education for students selecting the Bioprocess Engineering option within the curriculum, the author has revised the content of the course to give the students an opportunity to understand that different unit operations can be applied in various industries, namely food, biochemical, and biotechnology. The experiments have been decreased from 14 to 8 so the students could have a better grasp of the theories and applications. Students’ responses showed that it is important to design the experiments in a way to stimulate their desire to learn and perform. The author found that it is possible to give the students a better view of the various unit operations in bioprocess engineering. Page 9.1342.1 Page 1 Introduction As defined by Shuler and Kargi (2002), “Bioprocess engineers are engineers working to apply the principles of various disciplines, such as chemical, mechanical, electrical, and industrial, to processes based on using living cells or subcomponents of such cells.” In other words, bioprocess engineers are engineers who process biological materials to produce useful goods for society. Without question, bioprocess engineering is a broad-based engineering discipline. As educators, it is our job to broaden the view of the students, so they can take advantage of numerous, diverse job opportunities presented to them when they finish their BS degree. -
Method 3520C: Continuous Liquid-Liquid Extraction, Part of Test
METHOD 3520C CONTINUOUS LIQUID-LIQUID EXTRACTION 1.0 SCOPE AND APPLICATION 1.1 This method describes a procedure for isolating organic compounds from aqueous samples. The method also describes concentration techniques suitable for preparing the extract for the appropriate determinative steps described in Sec. 4.3 of Chapter Four. 1.2 This method is applicable to the isolation and concentration of water-insoluble and slightly soluble organics in preparation for a variety of chromatographic procedures. 1.3 Method 3520 is designed for extraction solvents with greater density than the sample. Continuous extraction devices are available for extraction solvents that are less dense than the sample. The analyst must demonstrate the effectiveness of any such automatic extraction device before employing it in sample extraction. 1.4 This method is restricted to use by or under the supervision of trained analysts. Each analyst must demonstrate the ability to generate acceptable results with this method. 2.0 SUMMARY OF METHOD 2.1 A measured volume of sample, usually 1 liter, is placed into a continuous liquid-liquid extractor, adjusted, if necessary, to a specific pH (see Table 1), and extracted with organic solvent for 18 - 24 hours. 2.2 The extract is dried, concentrated (if necessary), and, as necessary, exchanged into a solvent compatible with the cleanup or determinative method being employed (see Table 1 for appropriate exchange solvents). 3.0 INTERFERENCES 3.1 Refer to Method 3500. 3.2 The decomposition of some analytes has been demonstrated under basic extraction conditions required to separate analytes. Organochlorine pesticides may dechlorinate, phthalate esters may exchange, and phenols may react to form tannates. -
Making Downstream Processing Continuous and Robust a Virtual Roundtable S
BIOPROCESS TECHNICAL Making Downstream Processing Continuous and Robust A Virtual Roundtable S. Anne Montgomery, Cheryl Scott, and Peter Satzer, with Margit Holzer, Miriam Monge, Ralph Daumke, and Alexander Faude urrent biomanufacturing is driven to pursue continuous processing for cost reduction and increased productivity, Cespecially for monoclonal antibody (MAb) production and manufacturing. Although many technologies are now available and have been implemented in biodevelopment, implementation for large-scale production is still in its infancy. In a lively roundtable discussion at the BPI West conference in Santa Clara, CA (11 March 2019), participants touched on a number of important issues still to be resolved and technologies that are still in need of implementation at large scale. Below, moderator Peter Satzer (senior scientist RENTSCHLER BIOPHARMA (WWW.RENTSCHLER-BIOPHARMA.COM) with the Austrian Center of Industrial Biotechnology, Vienna) summarizes key points raised in that session. Based on Requirements for integration without the need for hold his highlights, BPI asked a number of Continuous Downstream tanks between unit operations requires industry representatives to comment on further exploration. those points further, and their Applications Chromatography Operations: Some responses follow. by Peter Satzer unit operations such as flow-through chromatography and single-pass, Minimizing Buffer and Hold Tanks: One tangential-flow filtration (SPTFF) can be critical parameter is integration of unit integrated easily into a continuous Product Focus: Biologics operations on manufacturing shop downstream process scheme at any floors using minimum numbers of point because they offer constant inflow Process Focus: Downstream buffer tanks and hold tanks. The benefit and outflow of material. Such operations processing of continuous manufacturing can be can be called truly or fully continuous. -
Design of Filtration and Drying Operations
17 DESIGN OF FILTRATION AND DRYING OPERATIONS SARAVANABABU MURUGESAN,PRAVEEN K. SHARMA, AND JOSE E. TABORA Process Research & Development, Bristol-Myers Squibb Co, New Brunswick, NJ, USA 17.1 INTRODUCTION manufacturing of an active pharmaceutical ingredient pro- ceeds via a number of sequential chemical conversions In this chapter, we consider two important unit operations in during which some of the intermediates are isolated in the the pharmaceutical industry, filtration and drying. As part of solid form. Although the isolation of all the intermediates the manufacturing process of active pharmaceutical ingre- may require the implementation of a filtration and drying dients (APIs), these two operations follow naturally from the sequence, these two unit operations acquire extreme impor- main mechanism of isolation and purification used in this tance in the final step when the API is isolated. Both filtration industry, that is, crystallization. It is in fact the dominance of and drying operations play a significant role in the quality and crystallization as an isolation and purification technology the physical properties of the API. that dictates the corresponding use of filtration and drying. As unit operations, both filtration and drying have wide appli- cability in the broad chemical and pharmaceutical industry; 17.2 FILTRATION however, for brevity and clarity we will limit our discussion here to situations in the pharmaceutical industry in which 17.2.1 Background and Principles these unit operations are a continuation of an isolation train that is preceded by a crystallization. In this context, the slurry In the pharmaceutical industry, filtration is the process of resulting from the crystallization is a mixture of the sus- separating solids from a supernatant by exposing the slurry to pended solids (valuable product) and the supernatant (waste a filter medium (filter cloth, screen, etc.) and applying solvent or mother liquor).