Edit filter log

''''Fractional distillation''' is the separation of a [[mixture]] into its component parts, or [[Fractionation|fractions]], such as in separating [[chemical compound]]s by their [[boiling point]] by heating them to a [[temperature]] at which one or more fractions of the compound will [[Vaporization|vaporize]]. It is a special type of [[distillation]]. Generally the component parts boil at less than 25&nbsp;°C from each other under a pressure of one [[atmosphere (unit)|atmosphere]]. If the difference in boiling points is greater than 25&nbsp;°C, a [[simple distillation]] is used. ==Laboratory setup== Fractional distillation in a laboratory makes use of common [[laboratory glassware]] and apparatuses, typically including a [[Bunsen burner]], a [[round-bottomed flask]] and a [[Condenser (heat transfer)|condenser]], as well as the single-purpose [[fractionating column]]. ===Apparatus=== [[Image:Fractional distillation lab apparatus.svg|thumb|300px|Fractional distillation <br> An [[Erlenmeyer flask]] is used as a receiving flask. Here the distillation head and [[fractionating column]] are combined in one piece.<ref name=HarwoodMoodyEOCPAP>{{cite book |author = Laurence M. Harwood, Christopher J. Moody |title = Experimental organic chemistry: Principles and Practice |edition = Illustrated |pages = 145–147 |isbn = 978-0-632-02017-1 |date=13 June 1989}}</ref>]] *heat source, such as a [[hot plate]] with a bath, and ideally with a magnetic stirrer. *distilling flask, typically a [[round-bottom flask]] *receiving flask, often also a round-bottom flask *[[fractionating column]] *distillation head *[[thermometer]] and adapter if needed *[[Condenser (heat transfer)|condenser]], such as a [[Liebig condenser]] or [[Allihn condenser]] *vacuum adapter (not used in image to the right) *[[boiling chip]]s, also known as anti-bumping granules *Standard [[laboratory glassware]] with [[ground glass joint]]s, e.g. [[quickfit apparatus]]. ===Discussion=== As an example consider the distillation of a mixture of water and [[ethanol]]. Ethanol boils at 78.4&nbsp;°C while water boils at 100&nbsp;°C. So, by heating the mixture, the most volatile component (ethanol) will concentrate to a greater degree in the vapor leaving the liquid. Some mixtures form [[azeotrope]]s, where the mixture boils at a lower temperature than either component. In this example, a mixture of 96% ethanol and 4% water boils at 78.2&nbsp;°C; the mixture is more [[Volatility (chemistry)|volatile]] than pure ethanol. For this reason, ethanol cannot be completely purified by direct fractional distillation of ethanol-water mixtures. The apparatus is assembled as in the diagram. (The diagram represents a batch apparatus as opposed to a continuous apparatus.) The mixture is put into the round bottomed flask along with a few [[Boiling chip|anti-bumping granules]] (or a Teflon coated magnetic stirrer bar if using magnetic stirring), and the fractionating column is fitted into the top. The fractional distillation column is set up with the heat source at the bottom on the still pot. As the distance from the stillpot increases, a temperature gradient is formed in the column; it is coolest at top and hottest at the bottom. As the mixed vapor ascends the temperature gradient, some of the vapor condenses and revaporizes along the [[temperature gradient]]. Each time the vapor condenses and vaporizes, the composition of the more volatile component in the vapor increases. This distills the vapor along the length of the column, and eventually the vapor is composed solely of the more volatile component (or an azeotrope). The vapor [[Condensation|condenses]] on the glass platforms, known as [[theoretical tray|trays]], inside the column, and runs back down into the liquid below, [[reflux]]ing distillate. The efficiency in terms of the amount of heating and time required to get fractionation can be improved by insulating the outside of the column in an insulator such as wool, aluminium foil or preferably a vacuum jacket. The hottest tray is at the bottom and the coolest is at the top. At steady state conditions, the vapor and liquid on each tray are at ''[[vapor–liquid equilibrium|equilibrium]]''. The most volatile component of the mixture exits as a [[gas]] at the top of the column. The vapor at the top of the column then passes into the condenser, which cools it down until it liquefies. The separation is more pure with the addition of more trays (to a practical limitation of heat, flow, etc.) Initially, the condensate will be close to the azeotropic composition, but when much of the ethanol has been drawn off, the condensate becomes gradually richer in water.{{citation needed|date=December 2013}} The process continues until all the ethanol boils out of the mixture. This point can be recognized by the sharp rise in temperature shown on the [[thermometer]]. The above explanation reflects the theoretical way fractionation works. Normal laboratory fractionation columns will be simple glass tubes (often vacuum-jacketed, and sometimes internally [[Silvering|silvered]]) filled with a packing, often small glass helices of 4 to 7&nbsp;mm diameter. Such a column can be calibrated by the distillation of a known mixture system to quantify the column in terms of number of theoretical trays. To improve fractionation the apparatus is set up to return condensate to the column by the use of some sort of reflux splitter (reflux wire, gago, Magnetic swinging bucket, etc.) - a typical careful fractionation would employ a reflux ratio of around 4:1 (4 parts returned condensate to 1 part condensate take off). In laboratory distillation, several types of condensers are commonly found. The [[Liebig condenser]] is simply a straight tube within a [[water jacket]], and is the simplest (and relatively least expensive) form of condenser. The [[Graham condenser]] is a spiral tube within a water jacket, and the [[Allihn condenser]] has a series of large and small constrictions on the inside tube, each increasing the surface area upon which the vapor constituents may condense. Alternate set-ups may use a multi–outlet distillation receiver flask (referred to as a "cow" or "pig") to connect three or four receiving [[Laboratory flask|flask]]s to the condenser. By turning the cow or pig, the distillates can be channeled into any chosen receiver. Because the receiver does not have to be removed and replaced during the distillation process, this type of apparatus is useful when distilling under an inert atmosphere for [[air-sensitive]] chemicals or at reduced pressure. A [[Perkin triangle]] is an alternative apparatus is often used in these situations because it allows isolation of the receiver from the rest of the system, but does require removing and reattaching a single receiver for each fraction. [[Vacuum distillation]] systems operate at reduced pressure, thereby lowering the boiling points of the materials. [[Boiling chip|Anti-bumping granules]], however, become ineffective at reduced pressures. ==Industrial distillation== [[Image:Colonne distillazione.jpg|right|thumb|250px|Typical industrial fractional distillation columns]] Fractional distillation is the most common form of separation technology used in [[oil refinery|petroleum refineries]], [[petrochemical]] and [[chemical plant]]s, [[natural gas processing]] and [[Air separation|cryogenic air separation]] plants.<ref name=Kister>{{cite book|author=Kister, Henry Z.|title= [[Distillation Design]]|edition=1st|publisher=McGraw-Hill|year=1992|isbn=0-07-034909-6}}</ref><ref name=Perry>{{cite book|author=Perry, Robert H. and Green, Don W.|title=[[Perry's Chemical Engineers' Handbook]]|edition=6th|publisher=McGraw-Hill|year=1984|isbn=0-07-049479-7}}</ref> In most cases, the distillation is operated at a [[Continuous distillation|continuous]] [[steady state]]. New feed is always being added to the distillation column and products are always being removed. Unless the process is disturbed due to changes in feed, heat, ambient temperature, or condensing, the amount of feed being added and the amount of product being removed are normally equal. This is known as continuous, steady-state fractional distillation. Industrial distillation is typically performed in large, vertical cylindrical columns known as "distillation or fractionation towers" or "distillation columns" with diameters ranging from about 65 centimeters to 6 meters and heights ranging from about 6 meters to 60 meters or more. The distillation towers have liquid outlets at intervals up the column which allow for the withdrawal of different fractions or products having different [[boiling points]] or boiling ranges. By increasing the temperature of the product inside the columns, the different hydrocarbons are separated. The "lightest" products (those with the lowest boiling point) exit from the top of the columns and the "heaviest" products (those with the highest boiling point) exit from the bottom of the column. For example, fractional distillation is used in [[oil refinery|oil refineries]] to separate [[crude oil]] into useful substances (or fractions) having different [[hydrocarbons]] of different boiling points. The crude oil fractions with higher boiling points: * have more [[carbon atom]]s * have higher [[molecular weight]]s * are more branched chain [[alkane]]s * are darker in color * are more [[viscosity|viscous]] * are more difficult to ignite and to [[combustion|burn]] [[File:Continuous Binary Fractional Distillation.PNG|frame|right|217px|Diagram of a typical industrial distillation tower]] Large-scale industrial towers use [[reflux]] to achieve a more complete separation of products. Reflux refers to the portion of the condensed overhead liquid product from a distillation or fractionation tower that is returned to the upper part of the tower as shown in the schematic diagram of a typical, large-scale industrial [[distillation]] tower. Inside the tower, the reflux liquid flowing downwards provides the cooling needed to condense the vapors flowing upwards, thereby increasing the effectiveness of the distillation tower. The more reflux is provided for a given number of [[theoretical plate]]s, the better the tower's separation of lower boiling materials from higher boiling materials. Alternatively, the more reflux provided for a given desired separation, the fewer theoretical plates are required. [[Image:Crude Oil Distillation.png||thumb|left|225px|[[Crude oil]] is separated into fractions by fractional distillation. The fractions at the top of the [[fractionating column]] have lower [[boiling point]]s than the fractions at the bottom. All of the fractions are processed further in other refining units.]] Fractional distillation is also used in air separation, producing [[liquid oxygen]], [[liquid nitrogen]], and highly concentrated [[argon]]. Distillation of [[chlorosilane]]s also enable the production of high-purity [[silicon]] for use as a [[semiconductor]]. In industrial uses, sometimes a packing material is used in the column instead of trays, especially when low pressure drops across the column are required, as when operating under vacuum. This packing material can either be random dumped packing (1-3" wide) such as [[Raschig ring]]s or [[structured packing|structured sheet metal]]. Typical manufacturers are Koch, Sulzer and other companies. Liquids tend to wet the surface of the packing and the vapors pass across this wetted surface, where [[mass transfer]] takes place. Unlike conventional tray distillation in which every tray represents a separate point of [[vapor liquid equilibrium]] the vapor liquid equilibrium curve in a packed column is continuous. However, when modeling packed columns it is useful to compute a number of [[theoretical plate|"theoretical plates"]] to denote the separation efficiency of the packed column with respect to more traditional trays. Differently shaped packings have different surface areas and void space between packings. Both of these factors affect packing performance. ===Design of industrial distillation columns=== [[Image:Tray Distillation Tower.PNG|frame|right|Chemical engineering schematic of typical bubble-cap trays in a distillation tower]] Design and operation of a distillation column depends on the feed and desired products. Given a simple, binary component feed, analytical methods such as the [[McCabe–Thiele method]]<ref name=Perry/><ref name=Beychok>{{cite journal | last = Beychok | first = Milton | title = Algebraic Solution of McCabe-Thiele Diagram | journal = Chemical Engineering Progress | date = May 1951 }}</ref><ref name=SeaderHenley>{{cite book|author=Seader, J. D., and Henley, Ernest J.|title=Separation Process Principles|publisher=Wiley| location=New York|year=1998|isbn=0-471-58626-9}}</ref> or the [[Fenske equation]]<ref name=Perry/> can be used. For a multi-component feed, [[simulation]] models are used both for design and operation. Moreover, the efficiencies of the vapor–liquid contact devices (referred to as ''plates'' or ''trays'') used in distillation columns are typically lower than that of a theoretical 100% efficient [[equilibrium stage]]. Hence, a distillation column needs more plates than the number of theoretical vapor–liquid equilibrium stages. Reflux refers to the portion of the condensed overhead product that is returned to the tower. The reflux flowing downwards provides the cooling required for condensing the vapours flowing upwards. The reflux ratio, which is the ratio of the (internal) reflux to the overhead product, is conversely related to the theoretical number of stages required for efficient separation of the distillation products. Fractional distillation towers or columns are designed to achieve the required separation efficiently. The design of fractionation columns is normally made in two steps; a process design, followed by a mechanical design. The purpose of the process design is to calculate the number of required theoretical stages and stream flows including the reflux ratio, heat reflux and other heat duties. The purpose of the mechanical design, on the other hand, is to select the tower internals, column diameter and height. In most cases, the mechanical design of fractionation towers is not straightforward. For the efficient selection of tower internals and the accurate calculation of column height and diameter, many factors must be taken into account. Some of the factors involved in design calculations include feed load size and properties and the type of distillation column used. The two major types of distillation columns used are tray and packing columns. Packing columns are normally used for smaller towers and loads that are corrosive or temperature sensitive or for vacuum service where pressure drop is important. Tray columns, on the other hand, are used for larger columns with high liquid loads. They first appeared on the scene in the 1820s. In most oil refinery operations, tray columns are mainly used for the separation of petroleum fractions at different stages of oil refining. In the oil refining industry, the design and operation of fractionation towers is still largely accomplished on an empirical basis. The calculations involved in the design of petroleum fractionation columns require in the usual practice the use of numerable charts, tables and complex empirical equations. In recent years, however, a considerable amount of work has been done to develop efficient and reliable computer-aided design procedures for fractional distillation.<ref> {{cite book |last=Ibrahim |first=Hassan Al-Haj |editor-last=Bennett |editor-first=Kelly |title=Matlab: Applications for the Practical Engineer |publisher=Sciyo |date=2014 |pages=139-171 |chapter=Chapter 5 |isbn= 978-953-51-1719-3}}</ref> ==See also== *[[Azeotropic distillation]] *[[Batch distillation]] *[[Extractive distillation]] *[[Freeze distillation]] *[[Steam distillation]] ==References== {{reflist}} ==External links== *[http://www.cheresources.com/validatingzz.shtml Validating Your Binary VLE Data] *[http://www.chemheritage.org/EducationalServices/pharm/antibiot/activity/distil.htm Chemistry Activity: Fractional Distillation] {{Distillation}} {{DEFAULTSORT:Fractional Distillation}} [[Category:Distillation]] [[Category:Fractionation]] [[Category:Industrial processes]] [[Category:Laboratory techniques]] [[de:Destillation#Fraktionierte Destillation]] [[ja:蒸留#精留]]'