Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Supercritical fluids extraction using

Principles and Characteristics Supercritical fluid extraction uses the principles of traditional LSE. Recently SFE has become a much studied means of analytical sample preparation, particularly for the removal of analytes of interest from solid matrices prior to chromatography. SFE has also been evaluated for its potential for extraction of in-polymer additives. In SFE three interrelated factors, solubility, diffusion and matrix, influence recovery. For successful extraction, the solute must be sufficiently soluble in the SCF. The timescale for diffusion/transport depends on the shape and dimensions of the matrix particles. Mass transfer from the polymer surface to the SCF extractant is very fast because of the high diffusivity in SCFs and the layer of stagnant SCF around the solid particles is very thin. Therefore, the rate-limiting step in SFE is either... [Pg.85]

Supercritical fluid extraction uses a supercritical fluid (Box 25-2) as the extraction solvent.20 C02 is the most common supercritical fluid because it is inexpensive and it eliminates the need for costly disposal of waste organic solvents. Addition of a second solvent such as methanol increases the solubility of polar analytes. Nonpolar substances, such as petroleum hydrocarbons, can be extracted with supercritical argon.21 The extraction process can be monitored by infrared spectroscopy because Ar has no infrared absorption. [Pg.656]

H. Daimon and Y. Hirata, Direct coupling of capillary supercritical fluid chromatography with supercritical fluid extraction using modified carbon dioxide , J. High Resolut. Chromatogr. 17 809-813 (1994). [Pg.149]

Supercritical fluid extraction with carbon dioxide has been shown to be an excellent alternative to conventional solvent extraction for the removal of hydrocarbon pollutants from solid samples [4-7]. It is fast ( 30 minutes), nonpolluting, and relatively simple to implement. Additionally, recent work has shown that (supercritical fluid extraction using carbon dioxide is generally applicable to soil samples that have been contaminated with petroleum hydrocarbons ranging from those found in gasoline to those in medium crude oil (i.e., < C30) hydrocarbons) [8-10]. [Pg.89]

Supercritical CO2 extraction may be used in batch or continuous systems to fractionate anhydrous milk fat into fractions with specific properties in order to enhance its utilization (Arul et al., 1987 Bhaskar et al., 1993). Supercritical fluid extraction using CO2 provides an alternative to the use of... [Pg.304]

Experimental work on resolution of ibuprofen and c/.v-chrysanthemic acid by supercritical fluid extraction using carbon dioxide was carried out. The effects of extraction temperature and pressure were investigated on the yield and enantiomeric excess of extracts and raffinates. An efficient extraction procedure was developed for production of (-)-c/s-chrysanthemic acid and (+)-c75-chrysanthemic acid resulting in 90 % enantiomeric excess. [Pg.393]

Supercritical Fluid Extraction Use of supercritical fluid C02 to solubilize and extract additives (ii)... [Pg.20]

So far some very important aroma chemicals better known as flavor and fragrance chemicals used to be isolated and extracted from natural products such as essential oils, resinoids, extracts, etc. Solvent extraction, steam distillation or, more recently, supercritical fluid extraction using high pressure CO2 have been some of the important methods for isolation of the important flavor and fragrance chemicals. There is a wide range of aromatic chemicals both from natural sources or made by organic chemical synthesis which have been introduced in various finished products. They are never used in very pure form but are further formulated for specific... [Pg.60]

Supercritical fluid extraction using CO, with methanol liquid-liquid extraction of SFE eluate with n-hexane after complexation with DDTC Derivatisation by addition of propylmagnesium chloride Separation by CGC detection by MS (Lab. 04)... [Pg.469]

Supercritical fluid extraction using CO has long been an appealing technology to extract soybeans. At elevated temperatures and pressures (31°C and 73 bar, 88°F and 1,060 psi), a supercritical state is achieved where CO has the diffusivity of a gas and the density of a liquid and has significant oil solvency. A simplified flow diagram is... [Pg.375]

Da Porto, C Natolino, A Decorti, D. Extraction of proanthocyanidins from grape marc by supercritical fluid extraction using C02 as solvent and ethanol-water mixture as cosolvent. Journal of Supercritical Fluids 2014, 87, 59-64. [Pg.78]

Supercritical Fluid Extraction. Supercritical fluid (SCF) extraction is a process in which elevated pressure and temperature conditions are used to make a substance exceed a critical point. Once above this critical point, the gas (CO2 is commonly used) exhibits unique solvating properties. The advantages of SCF extraction in foods are that there is no solvent residue in the extracted products, the process can be performed at low temperature, oxygen is excluded, and there is minimal protein degradation (49). One area in which SCF extraction of Hpids from meats maybe appHed is in the production of low fat dried meat ingredients for further processed items. Its apphcation in fresh meat is less successful because the fresh meat contains relatively high levels of moisture (50). [Pg.34]

The concern by consumers about cholesterol has stimulated the development of methods for its removal. Three principal approaches are in the pilot-plant stages use of enzymes, supercritical fluid extraction, and steam distillation. Using known techniques, it is not possible to remove all cholesterol from milk. Therefore, FDA guidelines identify cholesterol-free foods as containing less than 2 mg cholesterol per serving, and low cholesterol foods as containing from 2 to 20 mg (37). [Pg.371]

Purifications of elfamycins have been described in the Hterature using Craig distribution (2,34), chromatography on Sephadex LH-20 (2,14,26) and Amberlite XAD-2 (10,17,19,26), supercritical fluid extraction (37), and chromatography on an Ito multilayer cod planet centrifuge (26,38). and nmr assignments of most elfamycins have been accompHshed (3,24,26,32). The characteristic uv spectra permits some differentiation (12) and bathochromic shifts associated with Al " complexation have been used to quantify efrotomycin (2, R = CH ) in feed premixes (39,40). [Pg.523]

Removing an analyte from a matrix using supercritical fluid extraction (SEE) requires knowledge about the solubiUty of the solute, the rate of transfer of the solute from the soHd to the solvent phase, and interaction of the solvent phase with the matrix (36). These factors collectively control the effectiveness of the SEE process, if not of the extraction process in general. The range of samples for which SEE has been appHed continues to broaden. Apphcations have been in the environment, food, and polymers (37). [Pg.242]

The development of methods of analysis of tria2ines and thek hydroxy metabohtes in humic soil samples with combined chromatographic and ms techniques has been described (78). A two-way approach was used for separating interfering humic substances and for performing stmctural elucidation of the herbicide traces. Humic samples were extracted by supercritical fluid extraction and analy2ed by both hplc/particle beam ms and a new ms/ms method. The new ms /ms unit was of the tandem sector field-time-of-flight/ms type. [Pg.246]

Separation Techniques. Current methods for separating fatty acids are by solvent crystaUi2ation or by the hydrophili2ation process. Other methods that have been used in the past, or perhaps could be used in the future, are panning and pressing, solvent extraction, supercritical fluid extraction, the use of metal salts in assisting in separation, separations using urea complexes, and adsorption/desorption. [Pg.90]

Adsorption and Desorption Adsorbents may be used to recover solutes from supercritical fluid extracts for example, activated carbon and polymeric sorbents may be used to recover caffeine from CO9. This approach may be used to improve the selectivity of a supercritical fluid extraction process. SCF extraction may be used to regenerate adsorbents such as activated carbon and to remove contaminants from soil. In many cases the chemisorption is sufficiently strong that regeneration with CO9 is limited, even if the pure solute is quite soluble in CO9. In some cases a cosolvent can be added to the SCF to displace the sorbate from the sorbent. Another approach is to use water at elevated or even supercritical temperatures to facilitate desorption. Many of the principles for desorption are also relevant to extraction of substances from other substrates such as natural products and polymers. [Pg.2003]

Analytical Supercritical Fluid Extraction and Chromatography Supercritical fluids, especially CO9, are used widely to extrac t a wide variety of solid and hquid matrices to obtain samples for analysis. Benefits compared with conventional Soxhlet extraction include minimization of solvent waste, faster extraction, tunabihty of solvent strength, and simple solvent removal with minimal solvent contamination in the sample. Compared with high-performance liquid chromatography, the number of theoretical stages is higher in... [Pg.2004]

Supercritical fluid extraction (SFE) has been widely used to the extraction processes in pharmaceutical industries. Besides application of SFE in phannaceuticals, it has been applied on a wide spectmm of natural products and food industries such as natural pesticides, antioxidants, vegetable oil, flavors, perfumes and etc [1-2]. [Pg.365]

Supercritical fluid extraction (SFE) and Solid Phase Extraction (SPE) are excellent alternatives to traditional extraction methods, with both being used independently for clean-up and/or analyte concentration prior to chromatographic analysis. While SFE has been demonstrated to be an excellent method for extracting organic compounds from solid matrices such as soil and food (36, 37), SPE has been mainly used for diluted liquid samples such as water, biological fluids and samples obtained after-liquid-liquid extraction on solid matrices (38, 39). The coupling of these two techniques (SPE-SFE) turns out to be an interesting method for the quantitative transfer... [Pg.139]

S. A. Westwood (Ed.), Supercritical Fluid Extraction and its Use in Chromatographic Sample Preparation, CRC Press, Boca Raton, PE (1992). [Pg.148]

Supercritical fluid extraction (SFE) has been extensively used for the extraction of volatile components such as essential oils, flavours and aromas from plant materials on an industrial as well as an analytical scale (61). The extract thus obtained is usually analysed by GC. Off-line SFE-GC is frequently employed, but on-line SEE-GC has also been used. The direct coupling of SEE with supercritical fluid chromatography (SEC) has also been successfully caried out. Coupling SEE with SEC provides several advantages for the separation and detection of organic substances low temperatures can be used for both SEE and SEC, so they are well suited for the analysis of natural materials that contain compounds which are temperature-sensitive, such as flavours and fragrances. [Pg.241]

One example of normal-phase liquid chromatography coupled to gas chromatography is the determination of alkylated, oxygenated and nitrated polycyclic aromatic compounds (PACs) in urban air particulate extracts (97). Since such extracts are very complex, LC-GC is the best possible separation technique. A quartz microfibre filter retains the particulate material and supercritical fluid extraction (SPE) with CO2 and a toluene modifier extracts the organic components from the dust particles. The final extract is then dissolved in -hexane and analysed by NPLC. The transfer at 100 p.1 min of different fractions to the GC system by an on-column interface enabled many PACs to be detected by an ion-trap detector. A flame ionization detector (PID) and a 350 p.1 loop interface was used to quantify the identified compounds. The experimental conditions employed are shown in Table 13.2. [Pg.362]


See other pages where Supercritical fluids extraction using is mentioned: [Pg.230]    [Pg.8]    [Pg.916]    [Pg.130]    [Pg.152]    [Pg.275]    [Pg.170]    [Pg.61]    [Pg.192]    [Pg.170]    [Pg.3781]    [Pg.230]    [Pg.8]    [Pg.916]    [Pg.130]    [Pg.152]    [Pg.275]    [Pg.170]    [Pg.61]    [Pg.192]    [Pg.170]    [Pg.3781]    [Pg.74]    [Pg.226]    [Pg.242]    [Pg.165]    [Pg.91]    [Pg.116]    [Pg.136]    [Pg.141]    [Pg.144]    [Pg.250]    [Pg.251]    [Pg.303]   
See also in sourсe #XX -- [ Pg.624 ]

See also in sourсe #XX -- [ Pg.779 ]




SEARCH



Extractants supercritical fluid

Extraction of Organic Compounds from Ionic Liquids using Supercritical Fluids

Fluid extraction

Supercritical extractants

Supercritical extraction

Supercritical fluid extraction

Supercritical fluid extraction fluids

Use of supercritical fluid extraction

© 2024 chempedia.info