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Distillation basic principles

At low reflux ratios, the calculated number of stages will be very dependent on the accuracy of the vapor-liquid equilibrium data available. If the data are suspect, a higher than normal ratio should be selected to give more confidence in the design. [Pg.645]

The precise location of the feed point will affect the number of stages required for a specified separation and the subsequent operation of the column. As a general rule, the feed should enter the column at the point that gives the best match between the feed composition (vapor and liquid if two phases) and the vapor and liquid streams in the column. In practice, it is wise to provide two or three feed-point nozzles located around the predicted feed point to allow for uncertainties in the design calculations and data, and possible changes in the feed composition after startup. [Pg.645]

CONTINUOUS DISTILLATION BASIC PRINCIPLES 11.3.1. Stage Equations [Pg.645]

Material and energy balance equations can be written for any stage in a multistage process. [Pg.645]

CHAPTER 11 SEPARATION COLUMNS (DISTILLATION, ABSORPTION, AND EXTRACTION) [Pg.646]


ALCOHOL DISTILLATION BASIC PRINCIPLES, EQUIPMENT, PERFORMANCE RELATIONSHIPS, AND SAFETY... [Pg.1]

Distillers vary masking procedures, but generally conform to basic principles, especially in the maintenance of sanitary conditions. The cooking and conversion equipment is provided with direct or indirect steam, propeller agitation, and cooling coils. [Pg.84]

Vaporization and diffusion of flammable or toxic liquids or gases is a primary consideration with distillation, evaporation, extraction, and absorption operations. The basic principle of safety for tliese unit operations is contaimnent of the materials witliin the system. These operations should be conducted outdoors whenever possible. In tliis way, any accidental release of flammable or... [Pg.492]

Basic Principles of Operation Gas-separation literature often uses nomenclature derived from distillation, a practice that will generally be followed here. L is the molar feed rate, V is the molar permeate rate, R is the molar residue (L — V). Mole fractions of components i, j, in the feed-residue phase will be Xj, Xj. .. and in the permeate phase yi,yj.... Stage cut, 0, is permeate volume/feed volume, or V/L. [Pg.58]

The HI decomposition section flow sheets for both CEA and GA are heavily focused on efficient heat recovery. The basic principle for decomposition is the same for each. Reactive distillation of the HIX feed results in the production of hydrogen. The operating pressures in the distillation columns typically... [Pg.184]

The processes used in industrial air-separation plants have changed very little in basic principle during the past 25 years. After cooling the compressed air to its dew point in a main heat exchanger by flowing counter current to the products of separation, the air feed, at an absolute pressure of about 6 MPa, is separated in a double distillation column. This unit is kept cold by refrigeration developed in a turbine, which expands a flow equivalent to between 8 and 15% of the air-feed stream down to approximately atmospheric pressure. [Pg.180]

We cannot hope to cover the vast subject of distillation fundamentals and control in a single chapter in this book. Our objective here is to review some of the basic principles about distillation and then to summarize the essentials of distillation column control, particularly as it relates to the plantwide control problem. Many more details are available in the books cited above. In the first section we review some of the important fundamentals about distillation. Sections 6.3 through 6.8 discuss distillation column control mostly from the perspective of an isolated column or column system, This treatment presents what may appear to be a laundry list of control structures for different types of columns. Although we feel this presentation is valuable, particularly for the young inexperienced student or engineer, it is also vital to retain a broader plantwide perspective. Section 6.9 addresses some of these plantwide distillation control issues. In the next section we review the process fundamentals of distillation as they relate to process operation and control. [Pg.183]

When a product has been isolated from a reaction the next step is to purify it. The degree of purity required will depend on the use for which the sample is intended, a synthetic intermediate might only require rough purification, whereas a product for elemental analysis would require rigorous purification. This section describes the most important purification techniques, crystallization, distillation, sublimation, and chromatography. It is assumed that the reader is familiar with the basic principles of these methods, so the emphasis is on more demanding applications such as the purification of air-sensitive materials, and purifications on a micro-scale. [Pg.184]

Fooler The Elements of Chemical Kinetics and Reactor Calculations A Self-Paced Approach Himmelblau Basic Principles and Calculations in Chemical Engineering, 5th edition Holland Fundamentals and Modeling of Separation Processes Absorption, Distillation, Evaporation, and Extraction... [Pg.744]

Skill 12.1 Demonstrating knowledge of various separation techniques (e.g., distillation, filtration, chromatography) and their basic principles... [Pg.149]

The purpose of this publication is to help you understand the distillation of ethyl alcohol. It first presents the basic principles involved in distillation and how the process works. The types of distillation equipment and systems that might be involved in a small fuel alcohol plant are then discussed, as are the performance and control criteria needed for a general evaluation of each. The publication concludes with a discussion of safety, along with some general selection, operation and management criteria useful in evaluating alternatives. [Pg.1]

Winters, R.L. (1990) Deodorizer distillate, in Proc. World Conf. Edible Fats and Oils Processing, Basic Principles and Modem Practices (ed D.R. Erickson), AOCS Press, Champaign, IL, pp. 402-405. [Pg.58]

When chromatographic separations (7) are operated in a batch mode, a portion of the mixture to be separated is introduced at the column inlet. A solute-free carrier fluid is then fed continually through the column, the solutes separating into bands or zones. Some industrial operations such as mixed-vapor solvent recovery and sorption of the less volatile hydrocarbons in natural gas or natural gasoline plants are being carried out on pilot plant and semiworks scales. Continuous countercurrent systems designed along the basic principles of distillation columns have been constructed. [Pg.24]

Reviewing what has been said above, we reahze that the basic principles of distillation were already known in antiquity and in the middle ages, in spite of the simple equipment then available. UntQ the middle of the 19th century, laboratory and semi-... [Pg.30]

For the separation of the liquid feed M (composition x ) into two streams of composition Xg (product, distillate) and Xf, (bottom product), the required number of theoretical plates can be determined graphically with the aid of the McCabe-Thiele method, which was used in the past because no computers were available to solve the extensive systems of equations for mass balances and equilibrium relationships. This method is no longer of practical importance, but it is an excellent didactic aid for understanding the basic principles of rectification. [Pg.102]

The rate of elution of a component of the mixture is determined by the relative affinities of the component for the stationary and mobile phases. In gas chromatography, the elution rate is most often expressed as a retention time, defined as the time between the placement of the sample on the column and the maximum elution of the component in question. The basic principle responsible for the great utility of all chromatographic methods is the same Even compounds with very similar structural features frequently are eluted from the column at sufficiently different rates that an analytical or preparative separation is possible. If the efficiency of a gas chromatographic column is expressed in theoretical plates for comparison with distillation (Sec. 2.4.1), it is found that the gas chromatographic column provides 50 times as many theoretical plates as an efficient distillation column (e.g., a spinning-band column) of the same length. [Pg.73]


See other pages where Distillation basic principles is mentioned: [Pg.641]    [Pg.645]    [Pg.647]    [Pg.649]    [Pg.436]    [Pg.641]    [Pg.645]    [Pg.647]    [Pg.649]    [Pg.436]    [Pg.51]    [Pg.180]    [Pg.141]    [Pg.687]    [Pg.1042]    [Pg.276]    [Pg.509]    [Pg.51]    [Pg.6]    [Pg.132]    [Pg.45]    [Pg.475]    [Pg.51]   
See also in sourсe #XX -- [ Pg.497 , Pg.498 , Pg.499 , Pg.500 ]

See also in sourсe #XX -- [ Pg.492 ]




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