...Simple and Fractional Distillation Authors: Abion, T.J.J., Aganda, J.C., Alpay, R.F., Berboso, M.J.R., Casuga, J.M.D. (Group01-2A-BC) Abstract Distillation is the process of converting a liquid to a vapor, condensing the vapor, and then, collecting the distillate in another container. More about distillation will be discussed in the introduction. This experiment was carried out to differentiate simple from fractional distillation, to separate the components of an alcoholic drink, and to calculate the percentage of ethanol present in an alcoholic beverage. The group is assigned to do simple distillation. The computations performed for this experiment are the percent alcohol and percent loss. Percent alcohol determines the percentage of ethanol found in the beverage, while percent loss ascertains the amount of sample lost while doing the experiment. The experiment follows the distillation process to flammability test. The experiment follows as is in the procedure with some difficulties that will be seen in the latter part. Introduction Distillation is the process of purifying compounds by means of separating more volatile substance from non-volatile or less volatile substance. The analysts performed one of the two types of distillation processes- the simple distillation and fractional distillation. In simple distillation, the vapor emerging from the evaporating surface moves uniformly without contacting condensed liquid until they reach the condensing surface. Thus...
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...INTRODUCTION Distillation is a technique widely used in organic chemistry for separating compounds based on differences in their boiling points. The experiment is divided into two parts: simple distillation, an easy set-up where a solution or a mixture of substances with different volatility is separated through exposure heat; and fractional distillation, which under goes a series of evaporation and condensation process to purify more complex mixtures. Raoult and Dalton Law are the two principles involving with this experiment. The former states that the vapor pressure of a solvent above a solution is equal to the vapor pressure of the pure solvent at the same temperature scaled by the mole fraction of the solvent present. While the latter states that the total pressure of a gas in a container is the sum of the partial pressures of the individual gases in the container. In this experiment, the group performed a fractional distillation set-up. At the end of the day, they were able to attain the following objectives: differentiate simple from fractional distillation, separate the components of an alcoholic beverage and calculate the percentage of ethanol in a beverage. EXPERIMENTAL A. Compounds tested The compound or sample used in this experiment was vodka (alcohol). Vodka (35%–50%) was originally distilled from fermented wheat mash but now also made from a mash of rye, corn, or potatoes. In chemistry, an alcohol is an organic compound in which the hydroxyl functional...
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...Reflux is used to help carry a reaction to completion because the starting reagent has a slow reaction time. The purpose of reflux is to increase the reaction rate by boiling, but not to vaporize the products due to the low boiling points. The mixture of the starting material were heated first under reflux by increasing the rate of reaction through heating with a condenser attached because the temperature can be controlled while the condenser preserves the reagent by chilling the vapors. At the end of reflux, the mixture contained the products of each starting material. The mixture goes through reflux first because simple distillation does not allow enough time for the reaction to reach completion before separation. The solution goes through simple distillation after reflux to separate the products using the boiling points. For 1-propanol, the boiling point is around 97°C. Boiling point for 1-propanol is higher than the product produced, 1-bromopropane, which boils at around 72°C. The distillate should form around 72°C and should drop into the receiver at around 116°C, which creates the desired product of 1-bromopropane. The temperature range of...
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...VODKA BY MEANS OF SIMPLE DISTILLATION ABSTRACT: Cossack Vodka is distilled liquor composed primarily of water and ethyl alcohol or ethanol (CH3CH2OH) without a definite aroma or taste. Alcohol is a primary content of vodka, and distillation – a process involving condensation and evaporation wherein solvents of different boiling points are separated from each other – is a method that may be used to determine the certain presence of Alcohol content in Cossack vodka. A certain number (17) of test tubes were obtained, each with 0.05 ml until the temperature reached 93(C. The volume of distillate collected by the end of the experiment was 9.00 ml at 93(C, giving percent ethanol of 30.00 %. I. INTRODUCTION: Distillation is the process of evaporating a volatile substance from a solution of non-volatile substance wherein the vapor afterwards is condensed in the condenser and collected in the receiving flask. Simple distillation is a process of separating two liquids with different boiling points. It can be used to separate liquids with boiling points of at least fifty degree Celsius. There are four types of distillation: simple, fractional, vacuum, and azeotropic. Vodka is a colorless liquid made by distilling fermented substances such as sorghum, corn, rye or wheat. Vodka is said to contain 40% to 55% alcohol. The experiment aims to: (a) separate the components of Vodka, an alcoholic beverage, by the means of distillation, particularly simple distillation, (b) compute for the...
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...Azeotropic Distillation of water and ethanol by Harold van Schevensteen The process of simple distillation is a method of separating mixtures based on their differences in volatility in a boiling liquid mixture. We find out, however, that using this process, a mixture of water and ethanol cannot be separated fully. The latter can only be purified to approximately 96%. To get to this point, we go through a process whereby through distillation, we reduce the proportion of water in the mixture and increase that of ethanol. For example, if we were to distill a 50/50 mixture of ethanol and water, the distillate would be 80% ethanol and 20% water. Distilling this new mixture produces a mixture of 87% ethanol and 13% water. This goes on until we reach a ratio of 95.63% ethanol and 4.37% water, at which we reach a point called the azeotropic point of the mixture. At this stage, the mixture is called a positive azeotrope, which is defined when the ratio of the constituents cannot be further changed by simple distillation. This occurs because any further boiling of the mixture will result in a vapour who’s ratio of constituents is the same as the original mixture. The closer we get to this point, the lower the boiling point of the mixture as a whole. Ethanol has a boiling temperature of 78.4°C and water one of 100°C. When we have reached the azeotropic point, the mixture as a whole boils at a temperature of 78.2°C. Any further distillation will see the azeotrope boil at...
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...on the topic ‘Distillation Process’. I would also show my gratitude towards my Programme Leader Dr. Monika Thakur and our HOD Dr Amarinder Singh Bawa for including such a project in my course curriculum which gave me a chance to gain knowledge as much as I can in this field. Thank you Varun Gadodia BTech Food Technology IV semester Amity Institute of Food Technology Introduction This report examines the distillation process. This will enable the reader to understand the necessary components along with distillation calculations. Distillation is a process that separates two or more components into an overhead distillate and bottoms. The bottoms product is almost exclusively liquid, while the distillate may be liquid or a vapour or both. The separation process requires three things. First, a second phase must be formed so that both liquid and vapour phases are present and can contact each other on each stage within a separation column. Secondly, the components have different volatilities so that they will partition between the two phases to different extent. Lastly, the two phases can be separated by gravity or other mechanical means. Distillation differs from absorption and stripping in that the second phase is created by thermal means. The report also high lights the important equipments/methods used for distillation as well as its...
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...SIMPLE DISTILLATION OF VODKA (THE BAR) Somo, John Carlo , Sopoco, Marc Andrew , Sotong, Patricia , Venturina, Flian Lyra , Tia, Queenie de Leon 2B- Medical Technology Faculty of Pharmacy UST ABSTRACT Distillation is the method used for purifying liquids and separating mixtures of liquids into their individual components. The experiment targets to differentiate the two methods; simple and fractional distillation, to separate its water and alcohol components, and to determine the percentage of ethanol present in the vodka using simple distillation. A volume of 15mL vodka was poured into the distillation flask for heating/boiling by the alcohol lamp. 0.50 ml of distillate was collected in every calibrated test tube until the temperature reached 100 C. The initial/first and the final distillates were kept for the testing of flammability. The first distillate was the one containing the ethanol since it is flammable, while the other one is inflammable so it is the one with the purified water content. INTRODUCTION Distillation is the method of converting a liquid to vapor, condensing the vapor, and collecting the distillate in another container. It is used to separate liquids from nonvolatile solids, as in the separation of alcoholic liquors from fermented materials, or in the separation of two or more liquids having different boiling points, as in the separation of gasoline, kerosene, and lubricating oil from crude oil. In the modern organic chemistry laboratory, distillation is...
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...Distillation of Water Distilled water is water that has had many of its impurities removed through distillation. Distillation involves boiling the water and then condensing the steam into a clean container. Distilled water finds its use in a wide range of applications where the natural dissolved salts that water normally contains are not desirable. Some of these are topping up lead acid batteries, preparing aseptic solutions in hospitals, automotive cooling systems, steam irons, etc. Distilled water is not however, considered to be suitable for human consumption on a regular basis simply because it lacks the natural beneficial minerals that ordinary drinking water contains. Required materials: Beaker Rubber cork / tubing Bunsen burner Tripod stand Stand with clamp Basin filled with sand Impure (muddy) water Distilling flask with thermometer Liebig’s condenser with stand Step-By-Step Procedure 1. Pour the muddy water into the distilling flask. 2. Use the stand to hold the flask in place, supported by the tripod stand. 3. Place the burner below this. 4. Connect the pout of the distilling flask to one end of the Liebig’s condenser. 5. Position the Liebig’s condenser using its stand so that it slopes downward slightly; its pout (other end) must open directly above the beaker. 6. Bring the muddy water to a boil and collect the condensed liquid for observation. Note * Place the distilling flask in a sand basin before heating it – this will prevent vigorous boiling and damage thereof...
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...different speeds, causing them to separate. There are different types of chromatographic techniques such as column chromatography, TLC, paper chromatography, and gas chromatography. Paper chromatography is one of the important chromatographic methods. Paper chromatography uses paper as the stationary phase and a liquid solvent as the mobile phase. In paper chromatography, the sample is placed on a spot on the paper and the paper is carefully dipped into a solvent. The solvent rises up the paper due to capillary action and the components of the mixture rise up at different rates and thus are separated from one another. Distillation Simple distillation is a method used for the separation of components of a mixture containing two miscible liquids that boil without decomposition and have sufficient difference in their boiling points. The distillation process involves heating a liquid to its boiling points, and transferring the vapours into the cold portion of the apparatus, then condensing the vapours and collecting the condensed liquid in a container. In this process, when the temperature of a liquid rises, the vapour pressure of the liquid increases. When the vapour pressure of the liquid and the atmospheric pressure reach the same level, the liquid passes into its vapour state. The vapours pass over...
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...Separation of Hexane and Toluene Abstract The purpose of this lab was to separate hexane and toluene using the process of simple distillation. This was collected 3times each at different temperature and after collecting each distillate the refractive index was found of the distillate. Procedure The procedure is the same as Dr. Kelley provided and there were no changes made to it. Data | Fractional index | Temperature | First distillation | 1.3820 | 670c | Second distillation | 1.4656 | 1000c | Third distillation | 1.4851 | 1070c | Calculations X (1.3745) + (1-X) (1.4966) = nD This equation is for the volume fraction of X and the measured refractive index is nD. Found from the sheet of “simple distillation: separation of hexane and toluene” First distillate X (1.3745) + (1-X)(1.4966) = 1.3820 1.3745X - 1.4966X + 1.4966 = 1.3820 -0.1221X = -0.1146 X = 0.9386 1 – X = 0.0614 Volume fraction of Hexane = (X) * 100 = % =0.9386 * 100 = 93.86% Volume fraction of Toluene = (1- X) * 100 = % =0.0614 * 100 = 6.14% Second distillation X (1.3745) + (1-X)(1.4966) = 1.4656 1.3745X - 1.4966X + 1.4966 = 1.4656 -0.1221X = -0.031 X = 0.2539 1-X = 0.7461 Volume fraction of hexane = (X) * 100 = % 0.2539 * 100 = 25.39% Volume fraction of toluene = (1- X) * 100 = % 0.7461 * 100 = 74.61% Final distillation X(1.3745) + (1-X)(1.4966) = 1.4851 1.3745X - 1.4966X + 1.4966 = 1.4851 -0.1221X = -0.0115 X= 0.0942 1 – X = 0.9058 Volume...
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...Preparation of 1-Bromobutane The mechanism is SN2. The overall reaction is: H2SO4 + NaBr + CH3CH2CH2CH2OH 6 CH3CH2CH2CH2Br + H2O + NaHSO4 Boiling Point 118oC Boiling Point 92oC Day 1 CAUTION: Wear gloves during the entire experiment Fill out the table on your lab report form for this experiment INCLUDING YOUR NAME AND DATE and turn it in to the instructors box in NSM B-202 by 10:AM the day of the experiment. BE SURE TO DATE-STAMP YOUR LAB REPORT FORM USING THE DATE STAMP IN THE DEPARTMENT OFFICE (NSM-B-202) BEFORE PLACING IT INTO YOUR INSTRUCTORS BOX. FAILURE TO DO SO WILL RESULT IN YOUR FORM BEING MARKED "LATE". The report form will be returned to you in the lab. At your hood workstation, place a hotplate/stirrer atop a ringstand . Take a 250-mL round-bottomed flask, and clamp the flask to the ringstand, leaving about 1 inch of room between the bottom of the flask and a plastic bowl, whish sits atop the hotplate/stirrer.. Add 0.3 mole 1-butanol and ABOUT 35mL H2O to the flask and begin stirring the solution with the magnetic stirrer. CAREFULLY add 0.3 mole NaBr to the reaction flask. NOW, Add a slurry of ice and water to the bowl beneath the flask. S L O W L Y AND CAREFULLY add 35mL conc. H2SO4 to the flask. Remove the ice bath and replace it with a heating mantle. Add two or three boiling chips to the flask. Equip the flask with a reflux condenser and begin circulating...
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...INDUSTRIAL AND COMMERCIAL SETTINGS / DESIGNER CASE STUDY RESEARCH TASK FASHION DESIGN Fashion design - brand : CHANEL History of Chanel No.5 Chanel No.5 is the first perfume launched by French couturier Gabrielle "Coco" Chanel in 5 May, 1921. The chemical formula for the fragrance was compounded by French-Russian chemist and perfumer Ernest Beaux. The number 5 to Coco Chanel means good luck. She released this perfume on the 5th day of the 5th month and it's main sent is May rose and jasmine. Coco's famous quote on Chanel No.5 is “what is very important in a fragrance, is that the fragrance has some kind of mystery” The Chanel No.5 journey starts of in the fields of May roses at the Mul family's generations-old flower farm, in Pégomas, France. The weather is perfect for growing and picking roses: fresh and not too warm. Every single rose that goes into each bottle of No. 5 parfum is harvested by hand right there. A 30mL bottle of No. 5 parfum contains 1,000 jasmine flowers and 12 May roses - all from this same field. On average, it takes an hour and 20 minutes for a flower to go from being plucked in the field to being processed in the factory. Workers gently place the roses in the pockets of their aprons and transfer them into big burlap sacks; once these sacks are full, they’re loaded onto flatbed trailers and pulled by tractor back to the plant. Jean-Francois Vieille, a cousin of Joseph Mul’s, oversees operations at the prettily landscaped Sotraflor...
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...Simple and Fractional Distillation I. Introduction Distillation is one of the oldest and still most common methods for both the purification and the identification of organic liquids. It is a physical process used to separate chemicals from a mixture by the difference in how easily they vaporize. As the mixture is heated, the temperature rises until it reaches the temperature of the lowest boiling substance in the mixture, while the other components of the mixture remain in their original phase in the mixture. The resultant hot vapor passes into a condenser and is converted to the liquid, which is then collected in a receiver flask. The other components of the mixture remain in their original phase until the most volatile substance has all boiled off. Only then does the temperature of the gas phase rises again until it reaches the boiling point of a second component in the mixture, and so on. There are two types of distillation namely simple distillation and fractional distillation. In this experiment the efficiency of the two types of distillation will be compared. II. Methodology The following is the methods needed to perform fractional distillation. The gather the materials needed for the experiment such as the fractional distillation set-up, alcohol lamp, and vodka after which start performing the experiment. 1. Assemble the distillation set-up. 2. Prepare atleast 30 test tubes calibrated down to the 0.5 ml and number each test tube accordingly...
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...Determination of Percentage Ethanol from Gin Vodka by Simple Distillation *Bejasa,B. ; Beltran,R. ; Bombase,M. ; Bunyi,C. ; Canlas,L. 2BMT Abstract Vodka is composed primarily of water and ethanol with traces of impurities and flavourings and naturally has an alcoholic content of 38-40% by volume. This experiment aimed to determine the percent ethanol of the vodka through simple distillation. A 30mL of the sample was collected and heated through the use of alcohol lamp. A collection of 0.50mL of distillate was continuously made while recording its corresponding temperature until the sample reached 100°C. Through the obtained data, the percentage ethanol was computed (5.0%). Introduction Vodka is a clear liquor manufactured from ethyl alcohol. It is said to have been originally created from potatoes in Russia for medicinal purposes. Nowadays, Vodka is distilled from barley, wheat or rye. Most flavoured vodka contains 30-35% alcohol, whereas clear vodka is normally 40%, with a few brands offering a 50% product on top(1). Its percentage ethanol can be determined through the use of a simple distillation set-up. Simple distillation is designed to evaporate a volatile liquid from a solution of non-volatile substances(2). The first mention of the process of simple distillation appears in India and China around 800 B.C. in the production of beer and rice wine. At present time, simple distillation helps make production simple and economical, creating more products for consumers(3)...
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...Introduction Distillation is a procedure that has been used for many centuries as a separation technique to isolate liquids with different boiling points and vapor pressure. The idea of distillation generally involves the conversion of a solvent into a vapor then back to a solvent based on vapor pressure. The liquid with the lowest boiling point and highest vapor pressure would be collected first (Weldegirma,2017). There are various distillation methods, however the two methods utilize in this experiment are: simple and fractional using cyclohexane and Toluene. Simple distillation is more efficient when the boiling points are more than 25℃ difference and fractional distillation is more effective in separating liquids with boiling point less...
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