Pressurized liquid extraction principle

In this introductory book chapter, several modem extraction techniques will be described, including supercritical fluid extraction, pressurized liquid extraction, pressurized hot Avater extraction, microwave assisted extraction, membrane-assisted solvent extraction, solid phase micro extraction and stir-bar sorptive extraction. These are techniques that meet many of today s requirements in terms of environmental sustainability, speed and automation. Basic principles of operation as well as method optimization will be discussed and compared for the different techniques. Both analytical and industrial applications will be discussed, together with commercial instruments available on the market. Key references will be given, and conclusions regarding applicability of the different techniques with respect to sample e, target-molecules and analytical vs. large-scale applications. 

The mixture to be separated and analyzed may be either a gas, liquid, or a solid in some instances. All that is required is that the materials be stable, have a vapor pressure of 0.1 torr at the operating temperature and interact with the column material (either a solid adsorbent or a liquid stationary phase) and the mobile phase (carrier gas). The result of this interaction is the differing distribution of the sample components between the two phases, resulting in the separation of the sample components into zones or bands. The principle that governs the chromatographic separation is the foundation of most physical methods of separation, for example, distillation and liquid-liquid extraction. 

The same principle of operation as described above is applicable also to liquid-liquid extraction where an aqueous liquid and an organic liquid contact each other inside the contactor for extraction of a solute selectively from one phase to another [6-8]. The critical breakthrough pressure for liquid-liquid system could be calculated by Equation 2.1, except that the term A would now be the interfacial tension between the two liquids. Further variation of membrane contacting technology is called gas membrane or gas-gap membrane where two different liquid phases flow on either side of the membrane, but the membrane pores remain gas filled [9-10]. In this situation two separate gas-hquid contact interfaces are supported on each side of a single membrane. 

See also Chromatography Overview Principles. Dioxins. Extraction Solvent Extraction Principles Microwave-Assisted Solvent Extraction Pressurized Fluid Extraction. Food and Nutritional Analysis Oven/iew. Forensic Sciences Oven/iew. Gas Chromatography Overview. Lipids Oven/iew. Liquid Chromatography Overview. Pesticides. Pharmaceutical Analysis... 

See also Atomic Absorption Spectrometry Interferences and Background Correction. Atomic Emission Spectrometry Principles and Instrumentation Interferences and Background Correction Flame Photometry Inductively Coupled Plasma Microwave-Induced Plasma. Atomic Mass Spectrometry Inductively Coupled Plasma Laser Microprobe. Countercurrent Chromatography Solvent Extraction with a Helical Column. Derivatization of Analytes. Elemental Speciation Overview Practicalities and Instrumentation. Extraction Solvent Extraction Principles Solvent Extraction Multistage Countercurrent Distribution Microwave-Assisted Solvent Extraction Pressurized Fluid Extraction Solid-Phase Extraction Solid-Phase Microextraction. Gas Chromatography Ovenriew. Isotope Dilution Analysis. Liquid Chromatography Ovenriew. 

The ranges of temperatures and pressures, in which various separation methods (such as distillation, liquid extraction, gas chromatography (GC), supercritical fluid extraction (SFE), and chromatography (SFC)) are normally performed, are also marked in Fig. la. Here, SFE and SFC have to be attributed to conditions of temperatures and pressures exceeding the critical values, respectively. In principle. 

Fixed-roof atmospheric tanks require vents to prevent pressure changes which would othei wise result from temperature changes and withdrawal or addition of liquid. API Standard 2000, Venting Atmospheric and Low Pressure Storage Tanks, gives practical rules for vent design. The principles of this standard can be applied to fluids other than petroleum products. Excessive losses of volatile liquids, particularly those with flash points below 38°C (100°F), may result from the use of open vents on fixed-roof tanks. Sometimes vents are manifolded and led to a vent tank, or the vapor may be extracted by a recov-eiy system. 

Principles and Characteristics Water is an interesting alternative for an extraction fluid because of its unique properties and nontoxic characteristics. Two states of water have so far been used in the continuous extraction mode, namely subcritical (at 100 °C < T < 374 °C and sufficient pressure to maintain water in the liquid state) and supercritical (T>374°C, p>218 bar). Unfortunately, supercritical water is highly corrosive, and the high temperatures required may lead to thermal degradation of less stable organic compounds. However, water is also an excellent medium for extraction below its critical temperature [412], Subcritical water exhibits lower corrosive effects. 

Supercritical gas extraction depends on the fact that the vapour pressure of a solid or liquid can be greatly Increased by contacting It with a compressed gas, and that this enhancement Is the more pronounced the greater the gas density ). In principle, It Is consequently possible to transfer Into the vapour phase substances that are otherwise substantially non-volatlle. 

To understand any extraction technique it is first necessary to discuss some underlying principles that govern all extraction procedures. The chemical properties of the analyte are important to an extraction, as are the properties of the liquid medium in which it is dissolved and the gaseous, liquid, supercritical fluid, or solid extractant used to effect a separation. Of all the relevant solute properties, five chemical properties are fundamental to understanding extraction theory vapor pressure, solubility, molecular weight, hydrophobicity, and acid dissociation. These essential properties determine the transport of chemicals in the human body, the transport of chemicals in the air water-soil environmental compartments, and the transport between immiscible phases during analytical extraction. 

In principle many other solvent combinations could be used in biphasic chemistry although the main driving force in this area is to provide environmental benefits. For example, ionic liquids have been combined with supercritical solvents for the hydroformylation of 1-octene.30 Since ionic liquids are have no vapor pressure and are essentially insoluble in supercritical C02, the product can be extracted from the reaction using C02 virtually uncontaminated by the rhodium catalyst. 

---