i. Pressurized liquid extraction (PLE)
In 2010, Nieto et al. reported in his journal where this method is known with several names such as pressurized Fluid Extraction (PFE), accelerated fluid extraction (ASE), enhanced solvent extraction (ESE) and high pressure solvent extraction (HSPE). The concept of this method is the application of high pressure to remain solvent liquid beyond their normal boiling point. Simply means, high pressure facilitates the extraction process. Automation technique are the main reason for the greater development of PLE-based technique along with the decreased in extraction time and solvents requirement. Automation techniques are the technique where the sample is packed with inert material such as sand in the stainless
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The supercritical fluid has a higher diffusion coefficient and lower viscosity and surface tension than a liquid solvent, provide more penetration to a sample matrix and favourable mass transfer. The repeated flux of supercritical fluid to the sample provides complete extraction. The selectivity of supercritical fluid is higher than liquid solvent as its solvation power can be tuned either by changing temperature and/or pressure. Separation of solute from solvent in conventional extraction process can easily be bypassed by depressurization of supercritical fluid, which is time saving. SFE is operated at room temperature. Small amount of sample can be extracted compared with solvent extraction methods which will save time for overall experiment. SFE uses a little amount of organic solvent and considered as environment friendly. On-line coupling of SFE with chromatographic process is possible which is useful for highly volatile compounds. The recycling and reuse of supercritical fluid is possible and thus minimizing waste generation. SFE scale can be arranged on specific purpose from few milligram samples in laboratory to tons of sample in industries. SFE process provides information regarding extraction process and mechanism which can be manipulated to optimize the extraction
The purpose of this experiment was to learn and preform an acid-base extraction technique to separate organic compounds successfully and obtaining amounts of each component in the mixture. In this experiment, the separation will be done by separatory funnel preforming on two liquids that are immiscible from two layers when added together. The individual components of Phensuprin (Acetylsalicylic acid, Acetanilide, and Sucrose as a filler) was separated based upon their solubility and reactivity, and the amount of each component in the mixture was obtained. Also, the purity of each component will be determined by the melting point of the component.
The boiling point of the product was conducted with the silicone oil. Lastly, for each chemical test, three test tubes were prepared with 2-methylcyclohexanol, the product, and 1-decene in each test tube, and a drop of the reagent were added to test tubes. The percent yield was calculated to be 74.8% with 12.6g of the product obtained. This result showed that most of 2-methylcyclohexanol was successfully dehydrated and produced the product. The loss of the product could be due to the incomplete reaction or distillation and through washing and extraction of the product. The boiling point range resulted as 112oC to 118oC. This boiling point range revealed that it is acceptable because the literature boiling point range included possible products, which are 1-methylcyclohexene, 3-methylcyclohexene, and methylenecyclohexane, are 110 to 111oC, 104oC, and 102 to 103 oC. For the results of IR spectroscopy, 2-methylcyclocahnol showed peaks at 3300 cm-1 and 2930 cm-1, which indicated the presence of alcohol and alkane functional group. Then, the peak from the product showed the same peak at 2930 cm-1 but the absence of the other peak, which indicated the absence of the alcohol
The objective of this experiment is to separate a liquid mixture of Ethyl Acetate and Toluene through the process of Fractional Distillation. It is also to determine the mixture composition and the physical properties of the two liquids. Fractional Distillation “is used to separate (purify) the different liquid components of a mixture.”1 This type of distillation differs from Simple Distillation in which the mixture being used “is composed largely of a single liquid component.”1 Both processes use the liquids boiling point for the purification. If a liquid is gathering and the temperature corresponds to the theoretical boiling point of the liquid, then that liquid is what is being collected. The theoretical plate is “Each section of the
In this experiment, a mixture of three substances (benzoic acid, 2-naphthol, and 1-4 dimethoxybenzene) will be separated based off acidity strength using the liquid-liquid extraction technique through a separatory funnel. Benzoic acid and 2-napthol will be converted into ionic salts when reacting with their appropriate bases (sodium bicarbonate and sodium hydroxide). Both ionic salts will then form solids through the addition of acidic HCl. Neutral 1,4 – dimethoxybenzene forms a solid through the evaporation of ether. Each compound will then be purified through recrystallization, using the processes of dissolving the solid in either water or methanol, and isolating the solid through vacuum filtration. After a week of evaporation, the compounds will then be examined for both
The objective of this experiment was to perform extraction. This is a separation and purification technique, based on different solubility of compounds in immiscible solvent mixtures. Extraction is conducted by shaking the solution with the solvent, until two layers are formed. One layer can then be separated from the other. If the separation does not happen in one try, multiple attempts may be needed.
A convenient method of separating a mixture of organic compounds is recognized as liquid-liquid extraction, which involves the dispersion of a substance between two immiscible solvents using preferential solubility. Strategically using the differences in solubility of the interested solute, the compound can be transferred from one liquid part to the other during extraction. Organic acids and bases can be separated from each other by using an organic solvent like diethyl ether and a polar solvent such as water. Diethyl ether is an appropriate solvent since it wil...
Starting this experiment, we knew that the extraction was going to form varies layers due to the density differences. When placing three different substances, we saw that two layers formed because the Clove Oil is soluble in MTBE, but not in water. In order, to get the organic layer we used separatory funnel to take out the excess substances and leave the oil layer. Then we transferred to a beaker and dried with Magnesium Sulfate. Lastly, we filtered the liquid using funnel; we placed the liquid to boil, let it cool to room temperature. The purpose of drying and evaporation is to help us with the Gas Chromatography analysis of the product.
In this lab had to use acid- base extraction process. Since isopentyl acetate is soluble in diethyl ether, but acetic acid is soluble in both solvents. Therefore, a simple extraction procedure would remove only some of the acetic acid from isopentyl acetate, but it would not completely separate the two compounds.
Now days, this extraction technique was enhanced by the introducing an electrical potential. In this technique, which called electro membrane extraction (EME), the same setup for HF-LPME, plus the using of two electrodes. The driving force (which makes the extraction faster) in EME is the migration of the ions due to the response electrical potential. One electrode is put in the acceptor phase in the fibre, and the one is placed in the sample solution. That can be obvi...
The objective of this experiment was to use a common method of separation distillation. Distillation can be used in purifying or separating liquids, when the liquid if heated the more volatile component, the molecule with the lower boiling point, vaporizes and can be condensed. This type of separation will work efficiently when the feed mixture has a decent range between the boiling points of the components. The relationship between component’s vapor pressure to the composition of the solution is Ptotal==P1+P2, Raoult’s Law. This can be used with Dalton’s Law of partial pressure,
Remove the extra solvent on a steam bath under a hood while flushing the flask with N2 gas, leaving the crude extract. Weigh extract.
Once the mixture had been completely dissolved, the solution was transferred to a separatory funnel. The solution was then extracted twice using 5.0 mL of 1 M
In a practical application, fractional distillation could be used in environmental chemistry in order to
Chromatography and electrophoresis are used for many wonderful processes that take place in labs. Chromatography and electrophoresis are separation techniques employed by chemists. Chemists execute multiple chemical tasks daily therefore they must find the most efficient ways to carry out these functions. Even though electrophoresis has some benefits, Chromatography is more useful than electrophoresis because it is more versatile and can be widely used in research; chromatography should be used more than electrophoresis in scientific research because it is more effective in a lab setting and can be used in more fields.
HPLC (High Performance Liquid Chromatography) is an analytical technique which separates a complex mixture of components into its specific individual components. It is a powerful tool in analysis, as it combines high speed with extreme sensitivity compared to traditional methods of chromatography because of the use of a pump which creates a high pressure and forces the mobile phase to move with the analyte in high speed. It is been used as a principle technology in various automated analyzers used for diagnostic purpose.