Direct coupling of CO2 fluid extraction with capillary supercritical fluid chromatography

Summary An interface described in the literature was modified to accommodate small sample quantities. The simple and inexpensive method can be used to obtain rapid qualitative sample information of complex matrices by extraction in sub- or supercritical conditions (SFE) with a concurrent separation by capillary supercritical fluid chromatography (CSFC). Compared to traditional solvent extraction methods the potential for analyte degradation and contamination is minimized resulting in reduced sample amount necessary for extraction and separation, and also in faster extractions. Complex matrices of a plastic material, a natural product and a soil spiked with a substituted hydrocarbon test mixture were analyzed to show the usefulness of the interface.     

Theoretical optimization of analyte collection in analytical supercritical fluid extraction

Summary Optimizing the extracted analyte collection step in analytical supercritical fluid extraction (SFE) is of key importance in achieving high analyte recoveries and extraction efficiencies. Whereas the extraction step in SFE has been well characterized both theoretically and experimentally; the analyte collection step after SFE has few theoretical guidelines, aside from a few empirical studies which have appeared in the literature. In this study, we have applied several theoretical approaches using experimental data to optimize analyte trapping efficiency in SFE. A vapour-liquid equilibrium model has been formulated to predict the trapping efficiency for extracted solute collection in a open collection vessel. Secondly, a simple solution thermodynamic model for predicting solute (analyte) activity coefficients in various trapping solvents has been shown to have utility in predicting collection efficiencies. Finally, effective trapping efficiency after SFE using sorbent media is related to the extent of analyte breakthrough on the sorbent-filled trap after depressurization of supercritical fluid. Using experimental data determined via physico-chemical gas chromatographic measurements (i. e., specific retention volumes), we have shown the relationship between analyte breakthrough volume off of the trapping sorbent and volume of depressurized fluid through the collection trap. The above theoretical guidlines should prove of value to analysts in designing and optimizing the best conditions for trapping analytes after extraction via analytical SFE. Names are necessary to report factually on available data; however the USDA neither guarantees nor warrants the standard of the product, and the use of the name by USDA implies no approval of the products to the exclusion of others that may also be suitable.     

Efficiency of Different Methods and Solvents for the Extraction of Polycyclic Aromatic Hydrocarbons from Soils

The efficiencies of supercritical fluid extraction (SFE), accelerated solvent extraction (ASE), Soxhlet, and ultrasonic extraction in the analysis of polycyclic aromatic hydrocarbons (PAHs) in soils were evaluated. Solvents with different polarity were used to extract the PAHs from two soils, one with high and one with low contamination level. ASE showed good results with all solvents almost independent of the solvent polarity and the best results with acetone-toluene (1 : 1). Ultrasonic extraction with acetone-toluene for the uncontaminated soil and acetone-ethanolamine for the highly contaminated also showed good recoveries. The time-consuming Soxhlet extraction with pentane or dichloromethane was less effective. The PAH recovery from SFE was related to the soil matrix or the contamination level. The best extraction conditions (CO 2 /10% pentane) are successful for the soil with a low contamination level and a high humic acid content whereas the extractions of the highly contaminated soil gave poor results irrespective of the solvent used.     

土壤中烃类污染物的超临界流体萃取

采用超临界流体萃取技术提取环境样品中的烃类污染物，以色谱－质谱联用仪测定了萃取物的化学成分，考察了影响萃取效率的主要因素。比传统的索氏萃取能更有效地从复杂环境样品中萃取分析物。     

SFE of PAHs from soils with a high carbon content and analyte collection via combined liquid/solid trapping

Polynuclear aromatic hydrocarbons (PAHs) are recovered from a soil with a high carbon content (ca. 50%) with supercritical fluid extraction (SFE) as well as with conventional Soxhlet extraction. The influence of temperature and modifier volume on SFE efficiency and the effect of a combined liquid/solid trap for analyte collection are investigated in this study. Such traps, which make analyte collection and clean-up possible in one step, are compared with conventional analyte collection in pure organic solvents. A comparison between reproducibility and efficiency of SFE and Soxhlet extraction is presented.     

Supercritical fluid extraction of polyhalogenated pollutants from aquaculture and marine environmental samples: a review

This article focuses on the state-of-the-art in sample preparation using supercritical fluid extraction (SFE), to monitor the content of polyhalogenated pollutants in aquaculture and marine environmental samples. Marine sediments and biological applications, including several types of samples matrices (fish, shellfish, seaweed and fish feed) and analyte groups (polychlorinated biphenyls (PCBs), polybrominated biphenyls (PBBs), polybrominated diphenylethers (PBDEs), polychlorinated dibenzo-p-dioxin (PCDD)/Fs and organochlorinated pesticide (OCPs)) are discussed with respect to SFE use and optimisation of conditions. We also discuss the great analytical potential of SFE, the integration of the extraction and clean-up steps for rapid sample processing justifying its use for routine work. The most recent SFE applications to the determination of these pollutants in marine environmental (biota and sediment) samples, published in the last 15 years, are reviewed.     

Supercritical fluid extraction of aflatoxin B(1) from soil

This research describes the development of a supercritical fluid extraction (SFE) method to recover aflatoxin B(1) from fortified soil. The effects of temperature, pressure, modifier (identity and percentage), and extraction type were assessed. Using the optimized SFE conditions, the mean recovery from air dried soil was 72%. The variables associated with changes in recovery of aflatoxin were co-solvents, static extraction, and temperature. Acetonitrile-2% acetic acid, used both in-cell and on-line, provided the most efficient recovery. The results indicate that desorption from the soil was the limiting factor in recovery and that the static phase was more important than the dynamic.     

A Unified Sample Preparation System for Extraction of Various Analyte/Matrix Combinations

A supercritical fluid extraction/enhanced solvent extraction system (SFE/ESE) was used to remove polar and non-polar analytes from various matrices. Extraction of environmental pollutants from soil, additives from low density polyethylene, sulfa drugs from animal tissue, and drug from tablet was performed using both SFE and ESE. Results showed that a single instrumental system can be used to perform both ESE with organic solvents and SFE with carbon dioxide-based fluids. Each method has its own unique advantages and applications. The ability to carry out both solvent extraction and supercritical fluid extraction with one system has obvious economical advantages.     

Selective extraction of astaxanthin from crustaceans by use of supercritical carbon dioxide

An on-line supercritical fluid extraction (SFE) system coupled to a continuous flow manifold including a UV detector was used as a screening system to extract astaxanthin from crayfish, which was found to be the major carotenoid present in the samples. This compound constitutes the principal additive used to dye salmon flesh. The flow manifold was used to confirm the presence of astaxanthin in the crustacean samples. Also, an HPLC/UV-vis method was used to ascertain that this compound was the major carotenoid extracted under the optimum SFE conditions employed. The influence of SFE operating variables such as pressure, temperature, equilibration time, extraction time, trap temperature, and volume of CO₂ modifier was examined in order to maximize the efficiency of analyte extraction. The use of supercritical CO₂ enables the expeditious, selective, quantitative extraction of astaxanthin from crustaceans.     

Optimization of supercritical fluid extraction of pesticide residues in soil by means of central composite design and analysis by gas chromatography-tandem mass spectrometry

An environmentally friendly methodology is proposed for the analysis of pesticides in soil samples based on supercritical fluid extraction (SFE) and analysis at high selectivity and sensitivity, by gas chromatography-tandem mass spectrometry (GC-MS-MS). The pesticides investigated are among the most commonly used in intensive horticulture activities comprising organochlorine and organophosphorous insecticides, triazine and acetanilide herbicides, amongst others. An experimental design approach was used for modelling SFE and optimised extraction conditions were derived for the total pesticides extraction or for specific sub-groups of interest. Pesticide residues could be detected in soils in the sub-ppb range (0.1-3.7microgkg(-1)), with quite good precision (4.2-15.7%) and extraction efficiency (80.4-106.5%). The analysis of soil samples from an intensive horticulture area in Póvoa de Varzim, north of Portugal, revealed the presence of persistent pesticides, parent compounds and degradation products among the following: endosulfan, endosulfan sulfate, dieldrin, 4,4'-DDE, 4,4'-DDD, atrazine, alachlor, metolachlor, chlorpyrifos, pendimethalin and lindane. The important features to point out are the easy interpretation of chromatograms and straightforward confirmation of analytes that greatly facilitates the analyst judgement on the contamination of the sample.     

Correlation of supercritical-fluid extraction recoveries with supercritical-fluid chromatographic retention data: A fundamental study

The possibility of using supercritical-fluid chromatographic retention data for examining the effects of operational parameters, such as pressure and flow rate, on the extraction characteristics in supercritical-fluid extraction (SFE) was investigated. A model was derived for calculating the extraction efficiency in SFE from retention data and peak shapes measured in supercritical-fluid chromatography (SFC). By performing the SFC experiments at the same pressure and temperature as the SFE extractions using the SFE extraction cell as the SFC column, an accurate prediction of extraction efficiencies could be made. Finally, the effects of matrix composition and analyte concentration on extraction efficiency were studied.     

Dynamics of chelation-supercritical fluid extraction from wood fibers

The dynamics of supercritical fluid extraction (SFE) of the metal content of wood fibers chelated with lithium bis(trifluoroethyl) dithiocarbamate (FDDC) by supercritical (SF) CO2 was investigated experimentally by monitoring the spectra of the eluted metal complex as a function of time. The characteristic shape of the dynamic SFE curve was determined mainly by the flow conditions in the extraction vessel, the mass transfer resistance in the SF phase, and the solubility. High extraction yields of metal content were obtained in two-stage extraction including static (batch) and dynamic (semi-batch) stages. Increasing the length of the static stage increased the rate of dynamic elution of metal complex until it approached the dynamics of fluid displacement for a continuous stirred tank reactor (CSTR). In such cases, increasing the flow rate had no effect on the dynamic extraction curve when it was plotted using dimensionless time. Efficient chelation-SFE from wood fibers was obtained at a pressure of 20.3 MPa and with a static time of 30 min.     

Comparison of supercritical fluid and Soxhlet extractions for the isolation of nitro compounds from soils

Supercritical fluid extraction (SFE) with CO(2), a clean and rapid alternative to conventional Soxhlet extraction, was investigated for the extraction of nitro compounds from soil samples. Quantitative extraction by SFE was accomplished at a pressure of 25 MPa and an extraction temperature of 60 degrees C, for 30 min in dynamic mode and using acetonitrile as modifier, and the results were comparable with those obtained by acetonitrile Soxhlet extraction (3 h) for all soil samples. Extracts from these two procedures were analyzed by gas chromatography coupled with mass spectrometry. Quantitative reproducibility for SFE extracts was acceptable (RSD 2-10%), and the quantity of solvent was reduced from 160 mL for Soxhlet extraction to 5 mL in the case of SFE.     

环境模拟样品中多环芳烃的超临界流体萃取I．利用正交设计选择最佳萃取条件

采用正交设计实验方法，研究了从环境模拟样品中超临界流体萃取（ＳＦＥ）多环芳烃（ＰＡＨ）的最佳萃取条件。着重考察了超临界流体的压力、温度和用量等对萃取效率的影响。结果表明，压力的影响居第一位，温度影响次之，超临界ＣＯ２的用量的影响居第三位。建立了选择超临界流体萃取条件的简单方法     

Recovery of diesel fuel from soil by supercritical fluid extraction–gas chromatography

An analytical method based on CO₂ supercritical fluid extraction (SFE) followed by gas chromatography (GC) was evaluated, compared to Soxhlet extraction, and found to determine accurately and precisely diesel fuel contamination of standard soil samples at a total petroleum hydrocarbon level of 100 μg/g in soil. While both extraction methods have the same 3% relative repeatability standard deviation for determination of total hydrocarbon contamination at this level, SFE requires much less time, uses less organic solvent and provides better recovery of the more volatile n-C₁₀ to n-C₁₂ hydrocarbons.     

Thermodynamic and kinetic models for the extraction of essential oil from savory and polycyclic aromatic hydrocarbons from soil with hot (subcritical) water and supercritical CO2

Mechanisms that control the extraction rates of essential oil from savory (Satureja hortensis) and polycyclic aromatic hydrocarbons (PAHs) from historically-contaminated soil with hot water and supercritical carbon dioxide were studied. The extraction curves at different solvent flow-rates were used to determine whether the extractions were limited primarily by the near equilibrium partitioning of the analyte between the matrix and solvent (i.e. partitioning thermodynamics, or the "elution" step) or by the rate of analyte desorption from the matrix (i.e. kinetics, or the "initial desorption" step). Two simple models were applied to describe the extraction profiles obtained with hot water and with supercritical CO2: (1) a model based solely on the thermodynamic distribution coefficient KD, which assumes that analyte desorption from the matrix is rapid compared to elution. and (2) a two-site kinetic model which assumes that the extraction rate is limited by the analyte desorption rate from the matrix, and is not limited by the thermodynamic (KD) partitioning that occurs during elution. For hot water extraction, the thermodynamic elution of analytes from the matrix was the prevailing mechanism as evidenced by the fact that extraction rates increased proportionally with the hot water flow-rate. This was also confirmed by the fact that simple removal calculations based on a single KD (for each essential oil compound) gave good fits to experimental data for flow-rates from 0.25 to 4 ml/min. In contrast, supercritical CO2 extraction showed only minimal dependence on flow-rate, and the simple KD model could only describe the initial 20-50% of the extraction. However, a simple two-site kinetic model gave a good fit for all CO2 flow-rates tested. The results of these investigations demonstrated that very simple models can be used to determine and describe extractions which are limited primarily by partitioning thermodynamics, or primarily by desorption kinetics. Furthermore, these results show that the time required for the recovery of essential oil from savory with hot water can be minimized by increasing flow-rate, with little change in the total volume of water required. In contrast, raising the flow-rate of supercritical CO2 has little effect on the mass of essential oils recovered per unit of time, indicating that optimal recovery of these compounds with supercritical CO2 (amount recovered for the lowest amount of CO2) requires longer extraction times rather than faster flow-rates.     

The quantitative effect of microextractor cell geometry on the analytical supercritical fluid extraction efficiencies of environmentally important compounds

Summary The quantitative effect of microextractor cell geometries on supercritical fluid extraction (SFE) efficiencies of polycyclic aromatic hydrocarbons (PAHs) and methoxychlor from octadecyl-bonded sorbents has been evaluated and compared to similar effects seen upon increasing the supercritical fluid density. For the PAHs studied, correlations between the fused ring number and the relative increase in recoveries have been established. SFE recoveries can be increased by greater than a factor of two by decreasing the diameter to length ratio from 120 to 11. The relative recovery increase upon decreasing the diameter to length ratio of the extraction vessel is dependent on the analyte extractability, increasing in proportion to the fused ring number for the PAHs. Recoveries increased linearly as a function of supercritical fluid density for the PAHs studied. The change in the relative recovery upon increasing the supercritical carbon dioxide density again was dependent on the analyte type, decreasing linearly with fused ring number. Although fluid density generally had the greatest effect on achievable SFE recoveries, the cell geometry had effects of a similar order of magnitude, highly dependent on the initial extractability of the analyte.     

超临界二氧化碳萃取秋水仙碱（英文）

 利用超临界二氧化碳对秋水仙块根（经粉碎）中的秋水仙碱进行了萃取,采用高效液相色谱法对萃取出的秋水仙碱的质量分数进行了测定。实验选择40℃20～40MPa作为超临界苹取的操作条件,采用体积分数为95％的乙醇在索氏提取器中对样品进行了对比苹取实验。结果表明:不加浸泡剂进行浸泡处理的样品中的秋水仙碱很难被超临界二氧化碳萃取,在40℃,35MPa条件下,消耗1．28mol的二氧化碳只得到3％的萃取率。加入极少量的有机溶剂浸泡处理样品15min后再进行超临界萃取,可以极大程度地提高秋水仙碱的萃取率。     

Supercritical fluid extraction of polychlorinated biphenyls and pesticides from soil. Comparison with other extraction methods.

A comparison is made of supercritical fluid extraction (SFE) with two other techniques widely used for the extraction of polychlorinated biphenyls (PCBs) and organochlorine pesticides in soil. Extraction conditions for the SFE of PCBs and pesticides were first determined. An experimental approach was set up to determine the influence of different extraction parameters such as pressure, extraction time, static and dynamic extraction, restrictor type and collection solvent for off-line SFE. The use of carbon dioxide at 50 degrees C and 20 MPa, 10 min static followed by 20 min dynamic extraction with collection in iso-octane were been found to be the optimum conditions. Two types of soil, with a low and high content of organic carbon, respectively, spiked with 16 PCBs and organochlorine pesticides with a wide range of volatility and polarity at a level of 5 ng/g dry matter, were used as test materials. Conventional solvent extraction gives a good extraction yield for soil with a low content of organic carbon, but for peat soil the recoveries decrease dramatically to 30% for DDE, DDT and PCB 138 and 153. The recoveries with Soxhlet extraction are good, but an extra clean-up step before analysis is necessary. SFE gives good extraction yields for PCBs and organochlorine pesticides, varying between 85 and 105% with a reproducibility of 5% for each component for both types of soil. SFE is a fast, clean and reproducible method for the extraction of PCBs and organochlorine pesticides from these two soil matrices.     

Supercritical carbon dioxide extraction of volatiles from spices. Comparison with simultaneous distillation-extraction

Supercritical fluid extraction (SFE) and simultaneous distillation-extraction (SDE) were used to extract the essential oils from three different spices (oregano, basil, and mint), and a comparative study of extracts obtained using SFE and SDE is presented. Temperature and pressure for the SFE extraction were optimized prior to the experimental extractions. The extracts obtained using the two methods were very similar in composition, but SFE yielded better relative standard deviations and avoided the thermal degradation or solvent contamination of samples.