Supercritical assisted phase

When using supercritical fluids in place of liquids (non-solvent),an advanced, and greener, manufacturing approach to induce precipitation of the polymer can be achieved. This approach is commonly named the supercritical assisted phase inversion method (SAPIM) (Cardea et al, 2010). 

Duarte, A.R.C., Mano, J.F., Reis, R.L., 2009. Dexamethasone-loaded scaffolds prepared by supercritical-assisted phase inversion. Acta Biomaterialia 5, 2054-2062. 

In liquid-solid extraction (LSE) the analyte is extracted from the solid by a liquid, which is separated by filtration. Numerous extraction processes, representing various types and levels of energy, have been described steam distillation, simultaneous steam distillation-solvent extraction (SDE), passive hot solvent extraction, forced-flow leaching, (automated) Soxh-let extraction, shake-flask method, mechanically agitated reflux extraction, ultrasound-assisted extraction, y -ray-assisted extraction, microwave-assisted extraction (MAE), microwave-enhanced extraction (Soxwave ), microwave-assisted process (MAP ), gas-phase MAE, enhanced fluidity extraction, hot (subcritical) water extraction, supercritical fluid extraction (SFE), supercritical assisted liquid extraction, pressurised hot water extraction, enhanced solvent extraction (ESE ), solu-tion/precipitation, etc. The most successful systems are described in Sections 3.3.3-3.4.6. Other, less frequently... 

Ionic liquids have been described as designer solvents [11]. Properties such as solubility, density, refractive index, and viscosity can be adjusted to suit requirements simply by making changes to the structure of either the anion, or the cation, or both [12, 13]. This degree of control can be of substantial benefit when carrying out solvent extractions or product separations, as the relative solubilities of the ionic and extraction phases can be adjusted to assist with the separation [14]. Also, separation of the products can be achieved by other means such as, distillation (usually under vacuum), steam distillation, and supercritical fluid extraction (CO2). 

For the analysis of organic additives in polymeric materials, in most cases, prior extraction will be necessary. Depending on the nature of the additive, many different approaches are employed. These include soxhlet extraction with organic solvent or aqueous media, total sample dissolution followed by selective precipitation of the polymer leaving the additive in solution, assisted extraction using pressurised systems, ultrasonic agitation and the use of supercritical fluids. In trace analysis, solid phase extraction (SPME) from solution or solvent partition may be required to increase the analyte concentration. 

Supercritical fluid extraction (SFE), microwave-assisted extraction (MAE) and Soxhlet extraction under various experimental conditions were applied for spiked poly(vinyl) chloride samples. Extracted dyes were separated in an ODS column (250 X 4.6 mm i.d. particle size 5 jum) using methanol as the mobile phase. Dyes are well separated by this method as demonstrated in Fig. 3.59. The optimal parameters of the extraction methods are compiled in Table 3.23. Recoveries depended on both the type of extraction method and the chemical structure of the dye. It was found that the highest recovery can be obtained by MAE and the extraction efficacy was the lowest for Solvent red 24 [129],... 

Extraction of solid samples Homogenization extractions Sonication extractions Microwave assisted extractions Soxhlet extractions Accelerated solvent extractions Supercritical fluid extractions Extraction of liquid samples Liquid-liquid extractions Solid phase extractions (SPE)... 

The racemate of 1,3,2-benzodithiazole 1-oxide 42 was separated by supercritical fluid chromatography on the (A j )-Whelk-( )l column with supercritical carbon dioxide containing 20% methanol as a mobile phase. Peak areas of enantiomers prior to and after the separation, used for the calculation of the enantiomerization barrier, were detected by computer-assisted peak deconvolution of peak clusters registered on chromatograms using computer software <2002CH1334>. 

Extraction procedures of plant materials classical percolation, maceration, digestion, decoction, and so on, as well as supercritical fluid extraction, microwave-assisted extraction, pressurized solvent extraction, and solid-phase microextraction are described. Eor biological matrices, liquid-liquid, and solid phase extractions are mainly used for different samples such as blood, urine, microdialysates, and saliva, among others. 

Keywords Pressurized liquid extraction supercritical fluid extraction ultra-sound-assisted extraction microwave-assisted extraction matrix solid-phase extraction high-performance liquid chromatography gas chromatography liquid-liquid extraction solid phase extraction column chromatography... 

Depending on the complexity of the sample matrix, a pre-cleaning step is a possible solution to remove interfering eflFects nevertheless, the choice should be a good compromise in relation to the total time and cost of analysis [33]. Supercritical fluid- [48,49], microwave-assisted- [50] or solid-phase extraction (SPE) [51-53] have been used as pre-cleaning steps prior to immunoassay. However, in certain situations, the extraction step led to a decrease in accuracy and recovery, probably due to analyte loss during clean-up/ evaporation/re-dissolution steps [53]. 

The impact of the extraction conditions using various solvents on the recoveries has never been studied in detail, and the results have never been compared. The introduction of modern extraction methods, such as microwave-assisted extraction, supercritical fluid extraction, and solid-phase extraction, probably will improve the efficiency of extraction, even in the instance of unstable pigments and pigment mixtures. The majority of TLC separations were carried out on traditional silica layers. As the chemical structures and, consequently, the retention characteristics of pigments are highly different, a wide variety of eluent systems has been employed for their separation, consisting of light petroleum, ethyl formate, ethyl acetate, benzene, toluene, chloroform, methanol, n-butanol, formic or acetic acid, and so forth. 

Figure 6 Pressure effect on the temperature-induced and gas-assisted melting of tetracosane and PVDF (for more details and explanations, see refs. 26 and 29) (al) and (a2) heat rate evolution during fusion in the presence of supercritical CH and C 2 2 (VF), respectively (bl) fluid phase equilibria in the tetracosane/methane system and (b2) partial p—T phase diagram for the PVDF-VF and PVDF-N2 systems. Note the depression in the melting/crystallization temperatures in the pressure range up to 30 MPa for the tetracosane/CH and PVDF/VF systems...

First of all, it is important to identify what the acronyms represent. The following have been used aMAE, atmospheric microwave-assisted extraction SFE, supercritical fluid extraction pMAE, pressurized microwave-assisted extraction PFE, pressurized fluid extraction ASE, accelerated solvent extraction MSPD, matrix solid-phase dispersion. 

The focus in Chapters 7 and 8 is on the specific sample preparation approaches available for the extraction of organic compounds from environmental matrices, principally soil and water. Chapter 7 is concerned with the role of Soxhlet, ultrasonic and shake-flask extraction on the removal of organic compounds from solid (soil) matrices. These techniques are contrasted with newer developments in sample preparation for organic compound extraction, namely supercritical fluid extraction, microwave-assisted extraction and pressurized fluid extraction. Chapter 8 is arranged in a similar manner. Initially, details are provided on the use of solvent extraction for organic compounds removal from aqueous samples. This is followed by descriptions of the newer approaches, namely solid-phase extraction and solid-phase microextraction. 

The extraction techniques described in this book fulfill many of Anastas and Warner s principles. For example, the use of supercritical carbon dioxide (SC-CO2) as the sole extraction solvent results in a nonpolluting process (prevention of waste and safer solvents and auxiliaries). Other beneficial properties of supercritical CO2 include fast diffusivity and nearly zero surface tension, which lead to extremely efficient extractions. In Chapters 2-4, applications of SC-CO2 as an extraction solvent are described. Ethanol and water are also environmentally friendly solvents that can be used as extraction media in many applications (see Chapters 5-7). Pressurized hot water ( 100-200 °C) in particular is a safe and nonpolluting solvent that has a similar dielectric constant to polar organic solvents, such as ethanol or acetone. Hence, pressurized hot water is a viable green alternative to many current extraction processes that use toxic organic solvents. Similarly, pressurized hot ethanol is an excellent solvent for the extraction of most medium polar to nonpolar organic molecules. Some of the techniques, such as membrane-assisted solvent extraction, described in Chapter 10, use organic solvents but in much smaller amounts compared to classical extraction techniques. Other techniques, for instance solid-phase microextraction and stir-bar sorptive extraction, described in Chapter 11, use no solvents. 

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 procedure to be used to extract carbamate pesticides from environmental samples depends on their polarity and on the type of sample matrix involved. Various choices exist for the extraction of pesticides ranging from conventional procedures (e.g., Soxhlet extraction, liquid-liquid extraction (LLE), evaporation, steam distillation) to new methodologies including solid-phase extraction (SPE), solid-phase microextraction (SPME), supercritical fluid extraction (SEE), matrix solid-phase dispersion (MSPD), accelerated solvent extraction (ASE) and microwave-assisted extraction. " ... 

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