Search results for "liquid"

Sweeteners determination in table top formulations using FT-Raman spectrometry and chemometric analysis

2004

Abstract A partial least squares (PLS) Fourier transform Raman spectrometry procedure based on the measurement of solid samples contained inside standard glass vials, has been developed for direct and reagent-free determination of sodium saccharin and sodium cyclamate in table top sweeteners. A classical 22 design for standards was used for calibration, but this system provides accuracy errors higher than 13% w/w for the analysis of samples containing glucose monohydrate. So, an extended model incorporating glucose monohydrate (23 standards) was assayed for the determination of sodium saccharin and sodium cyclamate in all the samples. Mean centering spectra data pre-treatment has been emplo…

Determination of pesticides and their degradation products in soil: critical review and comparison of methods

2004

18 páginas, 5 figuras, 5 tablas.

Quantitation of hydrophobicity in micellar liquid chromatography

1999

Abstract Micellar liquid chromatography (MLC) is shown to be a promising technique for measuring the hydrophobicity of solutes. The presence of micelles has a profound effect on the chromatographic characteristics of reversed-phase columns. The linear relationships between the logarithm, log k , of the retention factor and such diverse properties as the number of carbon atoms in homologous series, octanol–water partition coefficients and solvatochromic parameters, which are observed in conventional reversed-phase liquid chromatography (RPLC), are not usually valid in MLC. For series of compounds exhibiting a wide range of hydrophobicity, k itself is linearly related to these properties. The…

Determination of macrolide and lincosamide antibiotics by pressurised liquid extraction and liquid chromatography-tandem mass spectrometry in meat an…

2010

Abstract A total of 155 samples, including meat and milk, were analyzed using a method developed for determining five macrolide antibiotics: tilmicosin (TILM), tylosin (TS), spiramycin (SPM), erythromycin (ERY), and tulathromycin (TULA) and two lincosamide antibiotics: pirlimycin (PIRL) and lincomycin (LM). The method was performed by pressurised liquid extraction (PLE) coupled to LC–MS/MS using electrospray ionization in positive ion mode. 2.5 mL of milk or 2.5 g of meat were dispersed in ethylenediaminetetraacetic acid sodium salt 2-hydrate (EDTA) and sea sand. The PLE conditions as: solvent, temperature, pressure, static time, and cell size were optimized. The following analytical parame…

Gas assisted mechanical expression (GAME) as a promising technology for oil and phenolic compound recovery from tiger nuts

2015

Abstract The aim of this work was to investigate the potential of gas assisted mechanical expression (GAME) process as an innovative technology for oil extraction and polyphenol recovery from tiger nuts. GAME process was first studied by varying the supercritical carbon dioxide (SC-CO2) and the mechanical expression (ME) pressures (10–30 MPa), then was compared to separate processes applied alone, using either SC-CO2 or ME. The results showed that the better conditions for GAME were found using 20 MPa for SC-CO2 and 30 MPa for ME. Under these conditions, 50% of oil was released from tiger nuts after 10 min extraction, compared to only 10% and 20% when using SC-CO2 and ME separately at 20 an…

Taxane analysis by high performance liquid chromatography-Nuclear magnetic resonance spectroscopy ofTaxus species

1998

High performance liquid chromatography–nuclear magnetic resonance spectroscopic analyses of taxane diterpenoids from three Taxus species were carried out employing a stopped-flow technique. Several taxanes have been identified from 500 mg leaf samples without prior isolation. © 1998 John Wiley & Sons, Ltd.

Isobaric Vapor−Liquid and Liquid−Liquid Equilibria for Chloroform + Methanol + 1-Ethyl-3-methylimidazolium Trifluoromethanesulfonate at 100 kPa

2009

Isobaric vapor−liquid equilibria for the binary system chloroform + methanol as well as the vapor−liquid equilibria for the chloroform + methanol + [emim][triflate] ternary system have been obtained at 100 kPa using a recirculating still. The ternary ionic liquid (IL) system presents an immiscibility zone at high chloroform composition, which increases with the temperature. Liquid−liquid equilibria for this system have also been determined. The measured ternary vapor−liquid equilibrium data were correlated using the Mock’s electrolyte nonrandom two-liquid (NRTL) model which reproduces reasonably well the experimental values and predicts the total disappearance of the azeotrope when the mole…

Determination of procaine and tetracaine in plasma samples by micellar liquid chromatography and direct injection of sample

2001

A liquid chromatographic procedure is proposed for the determination of procaine and tetracaine in plasma samples with direct injection. The method uses a Spherisorb octadecylsilane ODS-2 C18 analytical column and a micellar mobile phase containing 0.15 M sodium dodecyl sulphate, 0.5% triethylamine at pH 2.5 and 10% propanol. The UV detection was carried out at 300 nm. Plasma sample preparation required only adequate dilution with the mobile phase before injection into the chromatographic system. The proposed method allows the determination of procaine and tetracaine in plasma at therapeutic levels.

High-performance liquid chromatography of trichothecenes

1981

Liquid–liquid equilibria of the systems isobutyl acetate+isobutyl alcohol+water and isobutyl acetate+isobutyl alcohol+glycerol at different temperatu…

2008

Abstract In this work, experimental liquid–liquid equilibria (LLE) data of the isobutyl acetate + isobutyl alcohol + water and isobutyl acetate + isobutyl alcohol + glycerol systems are presented. The LLE of both systems have been measured at 283.15 and 323.15 K. The NRTL and UNIQUAC models were applied to both ternary systems. The interaction parameters obtained from both models successfully correlated the equilibrium compositions. The experimental tie lines were compared to the values predicted by the UNIFAC method. Moreover, the solvent capabilities of water and glycerol were compared.