Home About us Contact
|
Home About us Contact | ||
|
|
||
Extraction Efficiency (extraction + efficiency)
Kinds of Extraction Efficiency Selected AbstractsRemoval and Recovery of UO2(??) from Water Samples Using 2,2,-Diamino-4,4,-bithiazole as a New Reagent for Solid Phase ExtractionCHINESE JOURNAL OF CHEMISTRY, Issue 4 2010Majid Soleimani Abstract A novel sensitive and simple method for rapid and selective extraction, preconcentration and determination of uranyl as its 2,2,-diamino-4,4,-bithiazole (DABTZ) complex by using octadecylsilica columns and spectrophotometry is presented. Extraction efficiency and the influence of flow rates of sample solution and eluent, pH, amount of DABTZ, type and least amount of eluent for elution of uranyl complex from columns, break-through volume and limit of detection were evaluated. Also the effects of various cationic and anionic interferences on percent recovery of uranyl were studied. Average extraction efficiency of ca. 90% was obtained by elution of the column with minimal amount of solvent in the presence of interferences. The average preconcentration factor, 136 and a detection limit 0.32 ng·mL,1 were obtained. The method was applied to the recovery and determination of uranyl in different water samples. [source] Solid-Phase Extraction of Metoprolol onto (Methacrylic acid- ethylene glycol dimethacrylate)-based Molecularly Imprinted Polymer and Its Spectrophotometric DeterminationCHINESE JOURNAL OF CHEMISTRY, Issue 4 2010Mohammad Saber Tehrani Abstract A new adsorbent for molecularly imprinted solid phase extraction (MISPE) of metoprolol was synthesized using methacrylic acid (MAA) as functional monomer and ethylene glycol dimethacrylate (EGDMA) as cross-linking agent causing a non-covalent, bulk, thermal radical-polymerization. Control polymer (non-imprinted polymer) was prepared under well defined conditions without the use of metoprolol. The synthesized polymers were characterized by IR spectroscopy, X-ray diffraction and thermal analysis techniques. This polymer was used for the rapid extraction and preconcentration of metoprolol from real samples prior to spectrophotometric determination. Extraction efficiency and the influence of flow rates of sample and stripping solutions, pH, type of eluent for elution of metoprolol from polymer, break through volume and limit of detection were studied. The detection limit of the proposed method is 0.4 ng·mL,1. The method was applied successfully to the recovery and determination of metoprolol in tablets, human urine and plasma samples. [source] Automated stir plate (bar) sorptive extraction coupled to high-performance liquid chromatography for the determination of polycyclic aromatic hydrocarbonsJOURNAL OF SEPARATION SCIENCE, JSS, Issue 14 2010Chunhe Yu Abstract Automated methods of PDMS/,-CD/divinylbenzene-coated stir plate sorptive extraction (SPSE) coupled to HPLC-fluorescence detector were reported for the first time. Three automation modes, static SPSE, circular flow SPSE and continuous flow SPSE, were evaluated and critically compared with stir bar sorptive extraction by using six polycyclic aromatic hydrocarbons as model analytes. It was found that the operable sample volume for circular flow SPSE and continuous flow SPSE was larger than that for static SPSE. Under the same extraction conditions, continuous flow SPSE exhibited the highest extraction efficiencies in all automated modes and manual stir bar sorptive extraction for the target compounds. Compared with the manual operation (approximately 5,10,min), automated SPSE required a relatively short time (117,180,s) to finish sampling, washing and sample loading. Besides being labor-saving and time-saving, automated SPSE has other advantages, such as no time limit and non-attended operation. The proposed continuous flow PDMS/,-CD/divinylbenzene-coated SPSE-HPLC-fluorescence detector was successfully applied to environmental water analysis. [source] Designing supercritical carbon dioxide extraction of rice bran oil that contain oryzanols using response surface methodologyJOURNAL OF SEPARATION SCIENCE, JSS, Issue 8 2008Chih-Hung Wang Abstract This study examines the supercritical carbon dioxide (SC-CO2) extraction of oryzanols contained rice bran oil from powdered rice bran. The extraction efficiencies and concentration factors of oryzanols, free fatty acids and triglycerides in the SC-CO2 extracts were determined. With top-flow type SC-CO2 extraction the total oil yield was 18.1% and the extraction efficiencies of oryzanols and triglycerides were 88.5 and 91.3% respectively, when 2750 g CO2 was consumed during the extraction of 35 g rice bran powder. The concentration factors of oryzanols and triglycerides in SC-CO2 -extracted oil were higher than in the Soxhlet n -hexane extracted oil. SC-CO2 extractions indicated that pressure can be used more effectively than temperature to enhance the extraction efficiency and concentration factor of oryzanols. A two-factor central composite scheme of response surface methodology was employed to determine the optimal pressure (300 bar) and temperature (313 K) for increasing the concentration of oryzanols in the SC-CO2 extracted oil. [source] Determination of gastrodin and vanillyl alcohol in Gastrodia elata Blume by pressurized liquid extraction at room temperatureJOURNAL OF SEPARATION SCIENCE, JSS, Issue 13 2007Eng Shi Ong Abstract Pressurized liquid extraction (PLE) at room temperature with a laboratory-assembled system was applied for the extraction of gastrodin (GA) and vanillyl alcohol (VA) in Gastrodia elata Blume. The proposed system setup for this current work was simpler as no heating and backpressure regulator was required. Extraction with PLE was carried out dynamically at a flow rate of 1.5 mL/min, at room temperature, under an applied pressure of 10,20 bars with an extraction time of 40,50 min. The extraction efficiencies of the proposed method using 20% aqueous ethanol were compared with heating under reflux using organic solvents such as methanol and ethanol/water (20:80) for different batches of medicinal plant materials. For the determination of GA and VA in G. elata Blume, the extraction efficiencies of PLE at room temperature were observed to be comparable with heating under reflux. The method precision was found to vary from 1.6 to 8.6% (RSD, n = 6) on different days. The marker compounds present in the various medicinal plant extracts were determined by gradient elution HPLC and HPLC/MS/MS. Our work demonstrated the possibility of implementation of PLE at room temperature and the advantages of minimizing the use of organic solvents in the extraction process. [source] Analysis of flavor and perfume using an internally cooled coated fiber deviceJOURNAL OF SEPARATION SCIENCE, JSS, Issue 7 2007Yong Chen Abstract A miniaturized internally cooled coated fiber device was applied for the analysis of flavors and fragrances from various matrices. Its integration with a CTC CombiPAL autosampler enabled high throughput for the analysis of analytes in complex matrices that required simultaneous heating of the matrices and cooling of the fiber coating to achieve high extraction efficiency. It was found that up to ten times increase of extraction efficiencies was observed when the device was used to extract flavor compounds in water, even when limited sample temperatures were used to preserve the integrity of target compounds. The extraction of the flavor compounds in water with the device was reproducible, with RSD not larger than 15%. The lower limits of the linear ranges were in the low ppb range, which was about one order of magnitude smaller than those obtained with the commercialized 100 ,m PDMS fibers. Exhaustive extraction of some perfume ingredients from a complex matrix (shampoo) was realized. All achieved recoveries were not less than 80%. The repeatability of the extraction of the perfume compounds from shampoo was better than 10%. The linear ranges were about 1,3000 ,g/g, and the LOD was about 0.2,1 ,g/g. The automated internally cooled coated fiber device was demonstrated to be a powerful sample preparation tool in flavor and fragrance analysis. [source] Application of water as a solvent in microwave-assisted extraction for analysis of PCBs and CBzs in fly ashJOURNAL OF SEPARATION SCIENCE, JSS, Issue 6 2005Yifei Sun Abstract Polychlorinated biphenyls (PCBs) and chlorobenzenes (CBzs) are two classes of dioxin precursors formed in municipal solid waste incinerators (MSWIs); they produce negative health effects similar to those of dioxins. Reducing the analytical time required for determining the concentrations of these compounds in MSWIs is important for quickly evaluating their importance and assessing associated health risks. In the present study, water is used as a safe and environmentally friendly solvent in microwave-assisted extraction (MAE) for PCB and CBz analyses. MAE is compared with traditional Soxhlet extraction (SE) to determine the extraction efficiencies. The evaluation of extraction efficiencies shows that MAE has a high extraction efficiency compared with that of SE when water content is lower than 60%. Furthermore, the extraction time and organic solvent consumption are reduced with MAE compared with SE. [source] Extraction of Lanthanides from Aqueous Solution by Using Room-Temperature Ionic Liquid and Supercritical Carbon Dioxide in ConjunctionCHEMISTRY - A EUROPEAN JOURNAL, Issue 6 2006Soufiane Mekki Dr. Abstract For the first time, the study of a three-step extraction system of water/ionic liquid/supercritical CO2 has been performed. Extraction of trivalent lanthanum and europium from an aqueous nitric acid solution to a supercritical CO2 phase via an imidazolium-based ionic liquid phase is demonstrated, and extraction efficiencies higher than 87,% were achieved. The quantitative extraction is obtained by using different fluorinated ,-diketones with and without the addition of tri(n -butyl)phosphate. The complexation phenomenon occurring in the room-temperature ionic-liquid (RTIL) phase was evidenced by using luminescence spectroscopy. [source] Temporal indication of cannabis use by means of THC glucuronide determinationDRUG TESTING AND ANALYSIS, Issue 11-12 2009Ute Mareck Abstract According to the regulations of the World Anti-Doping Agency (WADA), the use of cannabinoids is forbidden in competition. In doping controls, the detection of cannabinoid misuse is based on the analysis of the non-psychoactive metabolite 11-nor-9-carboxy-delta-9-tetrahydrocannabinol (carboxy-THC). The determination of values greater than 15 ng/mL in urine represents an adverse analytical finding; however, no accurate prediction of the time of application is possible as the half-life of carboxy-THC ranges between three and four days. Consequently the detection of carboxy-THC in doping control urine samples collected in competition might also result from cannabis use in out-of-competition periods. The analysis of the glucuronide of the pharmacologically active delta 9-tetrahydrocannabinol (THC-gluc) may represent a complementary indicator for the detection of cannabis misuse in competition. An assay for the determination of THC-gluc in human urine was established. The sample preparation consisted of liquid-liquid extraction of urine specimens, and extracts were analysed by liquid chromatography/tandem mass spectrometry (LC-MS/MS). Authentic doping-control urine samples as well as specimens obtained from a controlled smoking study were analysed and assay characteristics such as specificity, detection limit (0.1 ng/mL), precision (>90%), recovery (,80%), and extraction efficiency (90%) were determined. Copyright © 2010 John Wiley & Sons, Ltd. [source] Poly(methacrylic acid-ethylene glycol dimethacrylate) monolith in-tube solid-phase microextraction applied to simultaneous analysis of some amphetamine derivatives in urine by capillary zone electrophoresisELECTROPHORESIS, Issue 16 2005Fang Wei Abstract A method based on in-tube solid-phase microextraction and capillary zone electrophoresis (CZE) was proposed for simultaneously determining four amphetamines (amphetamine, methamphetamine, 3,4-methylenedioxyamphetamine, and 3,4-methylenedioxymethamphetamine) in urine. A poly(methacrylic acid-ethylene glycol dimethacrylate) monolithic capillary column, which can provide sufficient extraction efficiency, was introduced for the extraction of amphetamines from urine samples. The hydrophobic main chains and acidic pendant groups of the monolithic column make it a superior material for extraction of basic analytes from aqueous matrix. After extraction, the samples were analyzed by CZE. The best separation was achieved using a buffer composed of 0.1,M disodium hydrogen phosphate (adjusted to pH,4.5 with 1,M hydrochloric acid) and 20% methanol v/v, with a temperature and voltage of 25°C and 20,kV, respectively. By applying electrokinetic injection with field-amplified sample stacking, detection limits of 25,34,µg/L were achieved. Excellent method of reproducibility was found over a linear range of 0.1,5,mg/L. Determination of these analytes from abusers' urine sample was also demonstrated. [source] Slow desorption behavior of one highly resistant aromatic amine in Lake Macatawa, Michigan, USA, sedimentENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 12 2005Shihua Chen Abstract The desorption behavior of benzidine from Lake Macatawa (Holland, MI, USA) sediment was investigated in this study using batch solvent extraction method. Seven solvents were tested as the extracting reagents: Deionized water (DI), calcium chloride in DI (CaCl2), sodium hydroxide in DI (NaOH), acetonitrile (ACN), a mixture of acetonitrile and ammonium acetate in DI (ACNNH4OAc), methanol (MeOH), and hydrochloric acid in DI (HCl). These solvents are proposed to react with sediment-associated benzidine by different mechanisms (e.g., cation exchange, hydrophobic partitioning, and covalent binding). Three sets of sorption isotherm experiments were conducted separately in these seven solvents with a 7-d, three-week, and two-month contact time. The results demonstrated nonlinear isotherms with Freundlich 1/n values varying from 0.25 to 0.52. The desorption behavior of benzidine in the solvents was evaluated after the sorption of benzidine onto the sediment with same contact times of 7 d, three weeks, and two months. A two-stage model subsequently was applied to simulate the experimental data. The rapidly desorbing rate constants were on the order of one to two per day for ACN, ACN-NH4OAc, and NaOH solvents, and the slowly desorbing rate constants were on the order of 10,5 to 10,4/d. Sequential desorption experiment demonstrated low total extraction efficiency of less than 40%. Both the observed sorption and desorption phenomena suggested that hysteresis and/or mass-transfer limited diffusion may result in the slow desorption behavior observed in this study. [source] Effect of sample size on cyst recovery by flotation methods: Recommendations for sample processing during EU monitoring of potato cyst nematodes (Globodera spp.)EPPO BULLETIN, Issue 2 2008J. Bellvert Under EC Council Directive 2007/33/EC member states of the European Union are recommended to take soil samples ranging from 100 mL to >1500 mL to monitor populations of potato cyst nematodes [PCN] (Globodera spp.) in targeted fields. This study examines the effects of varying sample size on sample processing and cyst extraction using two widely used laboratory methods. Cyst recovery was stable using the Fenwick can from 100 mL up to the physical limits of the can. Recovery was significantly lower for low density 50 mL samples; however, this was partly due to a statistical artefact since higher numbers of cysts were lost from successively larger samples with constant cyst numbers (i.e. decreasing densities). The Schuiling centrifuge had functional limits of <100 mL and >500 mL. Outside this range, cyst recovery from low density samples was significantly reduced. Cyst recovery from samples of varying size, but with equal numbers of cysts was only constant above 100 mL. However, samples ranging from 200,500 mL were optimal for the Schuiling centrifuge. Cyst extraction efficiency was similar using both methods for samples ranging from 150 mL to 1500 mL, where larger samples were divided into <500 mL portions. However, processing times (i.e. cyst extraction and microscopic examination) and water consumption increased significantly with increasing sample size and were significantly higher when using the Fenwick can. [source] Enhancement of Light Extraction Through the Wave-Guiding Effect of ZnO Sub-microrods in InGaN Blue Light-Emitting DiodesADVANCED FUNCTIONAL MATERIALS, Issue 7 2010Ki Seok Kim Abstract The improvement of the light extraction efficiency (LEE) of a conventional InGaN blue light-emitting diode (LED) by the incorporation of one-dimensional ZnO sub-microrods is reported. The LEE is improved by 31% through the wave-guiding effect of ZnO sub-microrods compared to LEDs without the sub-microrods. Different types of ZnO microrods/sub-microrods are produced using a simple non-catalytic wet chemical growth method at a low temperature (90,°C) on an indium-tin-oxide (ITO) top contact layer with no seed layer. The crystal morphologies of needle-like or flat-top hexagonal structures, and the ZnO microrods/sub-microrod density and size are easily modified by controlling the pH value and growth time. The wave-guiding phenomenon within the ZnO rods is observed using confocal scanning electroluminescence microscopy and micro-electroluminescence spectra. [source] Evaluation of the extraction efficiency for polyphenol extracts from by-products of green kiwifruit juicingINTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 12 2009Dongxiao Sun-Waterhouse Summary The health benefits of fruits are attributable in part to their bioactive components such as phenolics and pectic polysaccharides. By-products derived from kiwifruit processing can be a good source of such bioactive compounds. Extracts were produced using different concentrations of ethanol in water (0%, 30%, 50%, 74% and 96% v/v) from by-products (skin, residue and pulp) of the green-fleshed kiwifruit (Actinidia deliciosa,Hayward') juicing process. The amounts of phenolic compounds and uronic acid (UA) as well as the phenolic composition in each extract were determined. Results show that different by-products contained different concentrations of phenolics and pectic polysaccharides. Based on total phenolic contents, 96% v/v ethanol appeared to be the best extraction medium. The 30% or 74% ethanolic dilution was the second best medium for phenolic extraction from skin and pulp/residue, respectively. Water was a good medium for extracting satisfactory quantities of phenolics as well as the highest concentration of pectic polysaccharides. Phenolic profiling by high-performance liquid chromatography (HPLC) was used to detect individual phenolic compounds in an extract. Results using HPLC showed that alkali pre-treatment has improved the extraction efficiency of phenolics as a function of alkali concentration, fruit tissue type, extraction media, by-product preparation method, and class of polyphenols. As a result more efficient methods for both extraction and characterisation of polyphenols could be evaluated. [source] Evaluation of rayon swab surface sample collection method for Bacillus spores from nonporous surfacesJOURNAL OF APPLIED MICROBIOLOGY, Issue 4 2007G.S. Brown Abstract Aim:, To evaluate US Centers for Disease Control and Prevention recommended swab surface sample collection method for recovery efficiency and limit of detection for powdered Bacillus spores from nonporous surfaces. Methods and Results:, Stainless steel and painted wallboard surface coupons were seeded with dry aerosolized Bacillus atrophaeus spores and surface concentrations determined. The observed mean rayon swab recovery efficiency from stainless steel was 0·41 with a standard deviation (SD) of ±0·17 and for painted wallboard was 0·41 with an SD of ±0·23. Evaluation of a sonication extraction method for the rayon swabs produced a mean extraction efficiency of 0·76 with an SD of ±0·12. Swab recovery quantitative limits of detection were estimated at 25 colony forming units (CFU) per sample area for both stainless steel and painted wallboard. Conclusions:, The swab sample collection method may be appropriate for small area sampling (10 ,25 cm2) with a high agent concentration, but has limited value for large surface areas with a low agent concentration. The results of this study provide information necessary for the interpretation of swab environmental sample collection data, that is, positive swab samples are indicative of high surface concentrations and may imply a potential for exposure, whereas negative swab samples do not assure that organisms are absent from the surfaces sampled and may not assure the absence of the potential for exposure. Significance and Impact of the Study:, It is critical from a public health perspective that the information obtained is accurate and reproducible. The consequence of an inappropriate public health response founded on information gathered using an ineffective or unreliable sample collection method has the potential for undesired social and economic impact. [source] Solvent extraction studies of Sm(III) from nitrate medium and separation factors of rare earth elements with mixtures of sec -octylphenoxyacetic acid and 1,10-phenthrolineJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 6 2010Shujuan Fan Abstract BACKGROUND: Liquid,liquid extraction is widely used for the separation of rare earths, among which synergistic extraction has attracted more and more attention. Numerous types of synergistic extraction systems have been applied to rare earths with high extraction efficiency and selectivities. In the present study, mixtures of sec -octylphenoxyacetic acid (CA12, H2A2) and 1,10-phenanthroline (phen, B) have been used for the extraction of rare earths from nitrate medium. The stoichiometry of samarium(III) extraction has been studied using the methods of slope analysis and constant molar ratio. The possibility of using synergistic extraction effects to separate rare earths has also been studied. RESULTS: Mixtures of CA12 and phen display synergistic effects in the extraction of rare earth elements giving maximum enhancement coefficients of 5.5 (La); 13.7 (Nd); 15.9 (Sm); 24.5 (Tb); 45.4 (Yb) and 12.3 (Y). Samarium(III) is extracted as SmHA4B3 with mixtures of CA12 and phen instead of SmHA4 when extracted with CA12 alone. The calculated logarithm of the equilibrium constant is 6.0 and the thermodynamic functions, ,H, ,G, and ,S, have been calculated as 4.3 kJ mol,1, , 33.7 kJ mol,1 and 129.7 J mol,1 K,1, respectively. CONCLUSION: Mixtures of CA12 and phen exhibit synergistic effects on rare earth elements. Graphical and numerical methods have been successfully used to determine their stoichiometries. The different synergistic effects may provide the possibility of separating yttrium from heavy lanthanoids at an appropriate ratio of CA12 and phen. Copyright © 2010 Society of Chemical Industry [source] Computer simulation of flow-sheets for the solvent extraction of uranium: a new route to delay the effect of chemical degradation of the organic phase during uranium recovery from acidic sulfate mediaJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 12 2009Alexandre Chagnes Abstract BACKGROUND: The extractants used in solvent extraction processes undergo degradation under thermal, chemical and radiolytical stresses. In the case of uranium plants, tri- n -octylamine, used as an extractant, slowly degrades into di- n -octylamine. Such degradation causes a gradual depletion of the uranium extraction isotherms and as a result, of the efficiency of uranium recovery from feed solutions. The present work highlights a new route to delay this depletion of the extraction efficiency, merely by optimizing the flow-sheets involved in the process. Five flow-sheets have been compared for uranium recovery from acidic sulfate media by a solution of 0.146 mol L,1 tri- n -octylamine in kerosene modified with 5% w/w 1-tridecanol and stripping with a 199 g L,1 Na2CO3 solution. These five flow-sheets include the classical counter-current flow-sheet with four mixers,settlers in extraction and three mixers,settlers in stripping and four unusual combined solvent extraction flow-sheets with two independent extraction stripping loops and with one or two feed inlets. RESULTS: Computer simulation supplied evidence of the strong influence of the studied flow-sheets on the sturdiness of the process. More precisely, the unusual combined solvent extraction flow-sheets appeared to be significantly more efficient than the classical counter-current one and it is shown that an advantage of this can be to delay the negative impact of gradual degradation of tri- n -octylamine on uranium recovery efficiency from acidic sulfate media. CONCLUSION: The replacement of classical counter-current flow-sheets with a unique extraction-stripping loop in unusual combined flow-sheets with two or more independent extraction-stripping loops and with one or more feed inlets is a fruitful approach to delay the periodic addition of fresh tri- n -octylamine necessary for counter-balancing the progressive degradation of the extraction solvent and, as a result, to delay the gradual depletion of the efficiency of uranium recovery. Copyright © 2009 Society of Chemical Industry [source] APPLICATION OF ULTRASONICATION OR HIGH-PRESSURE EXTRACTION OF FLAVONOIDS FROM LITCHI FRUIT PERICARPJOURNAL OF FOOD PROCESS ENGINEERING, Issue 6 2009K. NAGENDRA PRASAD ABSTRACT Litchi (Litchi chinensis Sonn.) fruit pericarp (LFP) contains a high amount of flavonoids, which could be used as natural antioxidants. Some emerging novel technologies, such as ultrasonic extraction (UE) and high-pressure extraction (HPE), have exhibited great potential for flavonoid extraction. Experiments were conducted to comparatively investigate the effects of conventional extraction (CE), 40-KHz UE and 200- or 400-MPa HPE on the extraction efficiency of flavonoids from LFP. After 30 min of extraction, the extract yield, total phenolic content, 1,1-diphenyl-2-picrylhydrazyl radical scavenging activity and superoxide anion scavenging ability were examined. The crude extract yields by the UE, 400 HPE and CE were 24, 30 and 1.83%, respectively. However, there were no significant differences (P > 0.05) in the total phenolic content and antioxidant activity tested among these three different extractions at the same concentration. In addition, two flavonoids, namely epicatechin and epicatechin gallate, were identified and quantified as the major compounds, while catechin and procyanidin B2 were identified as the minor compounds. The total flavonoid content detected was 0.65, 0.75, 0.29 and 0.07 mg/g dry weight by HPE at 200 and 400 MPs, UE, and CE, respectively. Thus, the HPE technique showed a higher efficiency in extracting flavonoids from LFP, and the HPE could reduce the extraction time and increase the amount of the extracted phenolics. PRACTICAL APPLICATIONS Litchi (Litchi chinensis Sonn.) is a subtropical fruit that originated in Southeast Asia. As litchi fruit is gradually accepted by consumers for its delicious taste and attractive red skin, litchi production has steadily increased in recent decades, with increasing exports to Europe and North America from both the southern and northern hemisphere production areas. Litchi fruit pericarp (LFP) accounts for approximately 16% by weight of the whole fresh fruit and is comprised of a significant amount of flavonoids. Therefore, LFP tissues may be considered an important source of dietary flavonoids. This work showed that HPE technique has a high efficiency in extracting flavonoids from LFP tissues, which may help the litchi industry develop new extraction methods to better utilize the flavonoids from LFP tissues. [source] Methodology Optimization for Quantification of Total Phenolics and Individual Phenolic Acids in Sweetpotato (Ipomoea batatas L.) RootsJOURNAL OF FOOD SCIENCE, Issue 7 2007M.S. Padda ABSTRACT:, Phenolic acids are one of the several classes of naturally occurring antioxidant compounds found in sweetpotatoes. Simplified, robust, and rapid methodologies were optimized to quantify total and individual phenolic acids in sweetpotato roots. Total phenolic acid content was quantified spectrophotometrically using both Folin,Denis and Folin,Ciocalteu reagents. The Folin,Ciocalteu reagent gave an overestimation of total phenolic acids due to the absorbance of interfering compounds (that is, reducing sugars and ascorbic acid). Individual phenolic acids were quantified by high-performance liquid chromatography (HPLC) using the latest in column technology. Four reversed-phase C18 analytical columns with different properties (dimensions, particle size, particle shape, pore size, and carbon load) were compared. Three different mobile phases using isocratic conditions were also evaluated. A column (4.6 × 150 mm) packed with 5-,m spherical silica particles of pore size 110 Å combined with 14% carbon load provided the best and fast separation of individual phenolic acids (that is, chlorogenic acid, caffeic acid, and 3 isomers of dicaffeoylquinic acid) with a total analysis time of less than 7 min. Among the 3 mobile phases tested, a mobile phase consisting of 1% (v/v) formic acid aqueous solution: acetonitrile: 2-propanol, pH 2.5 (70:22:8, v/v/v) gave adequate separation. Among the solvents tested, aqueous mixtures (80:20, solvent:water) of methanol and ethanol provided higher phenolic acid extraction efficiency than the aqueous mixture of acetone. [source] Deodorization of Fish Sauce by Continuous-Flow Extraction with Microbubbles of Supercritical Carbon DioxideJOURNAL OF FOOD SCIENCE, Issue 8 2000M. Shimoda ABSTRACT: Volatiles were removed from fish sauce by continuous-flow extraction with microbubbles of supercritical carbon dioxide. The extraction was done at 35 °C and CO2/sample flow ratio of 0.14 and 0.29 under pressures of 10 to 30 MPa. After the treatment at a CO2/sample flow ratio, 0.29 at 10 MPa, remaining percentage ((the concentration in treated sample/that in untreated one) × 100) was 5.2% trimethylamine, 8.0% S-methyl ethanethioate, 30% dimethyldisulfide, 55 to 61% aliphatic aldehydes, and 25 to 42% carboxylic acids. The increase in CO2 flow rate improved the extraction efficiency significantly, but no effect of pressure was observed. The odor intensities of treated samples were between 1/4 and 1/8 of the untreated fish sauce. [source] Toward greener separations of rare earths: Bifunctional ionic liquid extractants in biodieselAICHE JOURNAL, Issue 9 2010Yinghui Liu Abstract Ionic liquids (ILs) containing quaternary phosphonium cations and phosphonic acid anions were explored as novel extractants for rare earths (RE) separation. They were considered to be bifunctional ionic liquid extractants (bif-ILEs), since both cations and anions of ILs were involved in the extraction. Trihexyl(tetradecyl)phosphonium bis 2,4,4-trimethylpentylphosphinate (Cyphos IL 104), as a bif-ILE, together with propylene carbonate (PC), dimethyl carbonate (DMC), and soybean oil methyl ester (SBME, biodiesel) as diluents was employed in the extraction of RE(III) from aqueous solutions. Acidified Cyphos IL 104 (HNO3 -Cyphos IL 104) exhibited high solubility in three diluents, and higher extraction efficiency than bis(2,4,4-trimethylpentyl)phosphinic acid (Cyanex 272) because of the coextraction of RE(III) by quaternary phosphonium cation and phosphonic acid anion in organic phase. Additionally, this coextraction mechanism could eliminate the loss of IL. The physical properties and miscibility test results indicated that SBME was an excellent solvent for RE(III) extraction. © 2010 American Institute of Chemical Engineers AIChE J, 2010 [source] Extraction of propionic acid from model solutions: Effect of pH, salts, substrate, and temperatureAICHE JOURNAL, Issue 7 2009Amit Keshav Abstract Propionic acid can be successfully produced from fermentation broth once an efficient recovery method is available for the produced acid. Reactive extraction in this regard is a promising recovery method. pH, salt, substrate, and temperature studies are crucial in the extraction of propionic acid, because these parameters varied in actual fermentation broth. With this regard, effects of these were studied. Extraction from model solutions and salt or substrate containing systems is lower than what was obtained from normal aqueous solutions. Reason of this is the varying degree of hindrances of the salts on extraction of the acid. pH has very large effect on extraction efficiency of the extracting system. At pH > pKa of acid, very low extraction was obtained. Temperature was found to have no effect on the extraction from model solutions used. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source] Extractive bioconversion in a four-phase external-loop airlift bioreactorAICHE JOURNAL, Issue 7 2000Lidija Sajc The integration of biosynthesis and product separation can increase the productivity of immobilized plant cells in airlift bioreactors. Extractive bioconversion of anthraquinones was studied in an external-loop airlift bioreactor consisting of a riser, a downcomer, and two horizontal sections, while containing alginate-immobilized Frangula alnus cells, a continuous aqueous phase (nutrient solution), dispersed solvent phase (n-hexadecane or silicone oil), and gas bubbles. A simple mathematical model was developed to describe the cocurrent liquid-liquid extraction in the riser section of the bioreactor and to rationalize the measured product concentrations in the aqueous and solvent phase. The model equations were solved analytically in a dimensionless form and used to study the effects of flow conditions, solvent properties, product formation rate, droplet size, and contactor length on the extraction efficiency and product concentration profiles in the continuous and dispersed phase. [source] Ultrasound-assisted dispersive liquid,liquid microextraction coupled with capillary gas chromatography for simultaneous analysis of nine pyrethroids in domestic wastewatersJOURNAL OF SEPARATION SCIENCE, JSS, Issue 12 2010Hongyuan Yan Abstract A simple and rapid ultrasound-assisted dispersive liquid,liquid microextraction method coupled with GC-flame ionization detection was developed for simultaneous determination of nine pyrethroids in domestic wastewater samples. An ultrasound-assisted process was applied to accelerate the formation of the fine cloudy solution using small volume of disperser solvent, which markedly increased the extraction efficiency and reduced the equilibrium time. Various parameters affecting the extraction efficiency were investigated, including the type and volume of extraction solvent and disperser solvent, extraction and ultrasonic time. Good linearity was obtained for all analytes in the range of 0.8,100,,g/L with the correlation coefficient (r2),0.998. The recoveries at three spiking levels ranged from 75.3 to 101.2% with the RSD less than 8.7% (n=5). Under the optimum condition, the enrichment factors for the nine pyrethroids ranged from 728- to 1725-fold. This method offered a good alternative for routine analysis due to its simplicity and reliability. [source] Magnesium oxide microspheres as a novel solid-phase extraction sorbent for the determination of benzo[a]pyrene in environmental water samplesJOURNAL OF SEPARATION SCIENCE, JSS, Issue 12 2010Jing Jin Abstract Magnesium oxide microspheres were developed as a novel SPE sorbent for the determination of benzo[a]pyrene (BaP), one of the most potent carcinogenic agents, in environmental water samples. The parameters controlling the extraction efficiency, such as elution volume, flow rate, pH values, and breakthrough volume, were investigated in detail. Considering the facile preparation and satisfying recovery, a corresponding analytical method has been developed to determine the concentration of BaP in real tap water, river water, and seawater. The recoveries for the spiked BaP were excellent (94,101%). [source] Highly sensitive determination of tetrabromobisphenol A and bisphenol A in environmental water samples by solid-phase extraction and liquid chromatography-tandem mass spectrometryJOURNAL OF SEPARATION SCIENCE, JSS, Issue 11 2010Ru-Song Zhao Abstract Using bamboo-activated charcoal as SPE adsorbent, a novel SPE method was developed for the sensitive determination of tetrabromobisphenol A and bisphenol A in environmental water samples by rapid-resolution LC-ESI-MS/MS. Important parameters influencing extraction efficiency, including type of eluent, eluent volume, sample pH, volume and flow rate, were investigated and optimized. Under the optimal extraction conditions (eluent: 8,mL methanol, pH: 7; flow rate: 4,mL/min; sample volume: 100,mL), low LODs (0.01,0.02,ng/mL), good repeatability (6.2,8.3%) and wide linearity range (0.10,10,ng/mL) were obtained. Satisfied results were achieved when the proposed method was applied to determine the two target compounds in real-world environmental water samples with spiked recoveries over the range of 80.5,119.8%. All these facts indicate that trace determination of tetrabromobisphenol A and bisphenol A in real-world environmental water samples can be realized by bamboo-activated charcoal SPE-rapid resolution-LC-ESI-MS/MS. [source] Headspace solid-phase microextraction for direct determination of volatile phenols in ciderJOURNAL OF SEPARATION SCIENCE, JSS, Issue 21 2009Consuelo Pizarro Abstract A headspace solid-phase microextraction coupled to gas chromatography-tandem mass spectrometry (GC-MS/MS) method was optimised and validated for the determination of 4-ethylguaiacol, 4-ethylphenol, 4-vinylguaiacol and 4-vinylphenol, involved in the presence of Brett character, in ciders. The influence of different parameters on extraction efficiency (fibre coating, salt addition, exposure time, extraction temperature and sample volume/total volume ratio) was evaluated. Divinylbenzene/carboxen/PDMS was selected as extraction fibre and the other optimised parameters were as follows: 10,mL of cider, temperature 70°C, extraction time 60,min and addition of 0.4,g/mL of NaCl. The proposed method showed satisfactory linearity. The detection limits obtained were 0.01,,g/L for 4-ethylguaiacol, 0.02,,g/L for 4-ethylphenol, 0.08,,g/L for 4-vinylguaiacol and 0.03,,g/L for 4-vinylphenol. These detection limits were lower than those obtained in previous studies on the determination of volatile phenols in other alcoholic beverages. Good recoveries of over 95% were observed for all compounds, and the repeatability obtained was considered acceptable, ranging between 4 and 10%. To demonstrate the feasibility of the procedure, the method was applied to the analysis of commercial ciders. To our knowledge, this is the first time that the headspace solid-phase microextraction procedure has been optimised to determine specifically the Brett character responsible compounds in cider. [source] Influence of temperature on mass transfer in an incomplete trapping supported liquid membrane extraction of triazole fungicidesJOURNAL OF SEPARATION SCIENCE, JSS, Issue 7 2009Luke Chimuka Abstract The influence of temperature in a supported liquid membrane (SLM) extraction of triazole fungicides was investigated. The mass transfer parameters such as diffusion coefficient, flux and apparent viscosity were determined at temperatures ranging from 5 to 40°C. Increase in temperature led to an increase in diffusion coefficient and flux with a flowing acceptor solution. The apparent viscosity also decreased with an increase in temperature. However, the increase in mass transfer parameters did not result in an overall increase in extraction efficiency with a stagnant or circulation acceptor phase. Stripping of the analytes from the membrane into the acceptor phase as well as the configuration of the extraction unit could have limited the influence of temperature on mass transfer. The partition coefficient of analytes from the acceptor solution to the membrane, KA, was found to be much higher than that from the donor solution to the membrane KD, thus triazole compounds preferred to remain in the membrane even with an increased extraction temperature. [source] Application of continual injection liquid-phase microextraction method coupled with liquid chromatography to the analysis of organophosphorus pesticidesJOURNAL OF SEPARATION SCIENCE, JSS, Issue 4 2009Yanuardi Raharjo Abstract A liquid-phase microextraction coupled with LC method has been developed for the determination of organophosphorus pesticides (methidation, quinalphos and profenofos) in drinking water samples. In this method, a small amount (3 ,L) of isooctane as the acceptor phase was introduced continually to fill-up the channel of a 1.5 cm polypropylene hollow fiber using a microsyringe while the hollow fiber was immersed in an aqueous donor solution. A portion of the acceptor phase (ca. 0.4 ,L) was first introduced into the hollow fiber and additional amounts (ca. 0.2 ,L) of the acceptor phase were introduced to replenish at intervals of 3 min until set end of extraction (40 min). After extraction, the acceptor phase was withdrawn and transferred into a 2 mL vial for a drying step prior to injection into a LC system. Parameters that affect the extraction efficiency were studied including the organic solvent, length of fiber, volume of acceptor and donor phase, stirring rate, extraction time, and effect of salting out. The proposed method provided good enrichment factors of up to 189.50, with RSD ranging from 0.10 to 0.29%, analyte recoveries of over 79.80% and good linearity ranging from 10.0 to 1.25 mg/L. The LOD ranged from 2.86 to 82.66 ,g/L. This method was applied successfully to the determination of organophosphorus pesticides in selected drinking water samples. [source] Sensitive determination of phenols in environmental water samples with SPE packed with bamboo carbon prior to HPLCJOURNAL OF SEPARATION SCIENCE, JSS, Issue 4 2009Ru-Song Zhao Abstract Bamboo carbon, an inexpensive, readily available material, has attracted great attention in recent years because of adsorptive properties. In this paper, the potential of bamboo carbon as a SPE adsorbent for the determination of phenols, was investigated. Phenols are important environmental contaminants that may adversely affect human health. Parameters influencing extraction efficiency, including type of eluent, eluent volume, amount of adsorbent, as well as sample pH, volume, and flow rate were investigated and optimized. The optimized results exhibited excellent linear relationships between peak area and phenol concentrations over the range of 2.0,100 ng/mL, with precision between 2.2,7.2%. The LODs were 0.06,0.4 ng/mL for the eight phenols tested. The proposed method has been successfully applied to the analysis of several real-world environmental water samples. These results indicate that bamboo carbon may be used as a novel SPE adsorbent for the concentration and determination of phenols in real environmental water samples. [source] | ||||||||||||||||||||||||||||||||||