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981.
The influence of the vapors ofn-amyl orn-decyl alcohol on the stability of single thin liquid films, single bubbles, and foam columns was determined. It was found that the presence of surfactant vapors lowered the stability of foams and single foam films. The mechanism of the destabilizing action of the surfactant vapors on wet, dynamic foams under dynamic conditions is discussed. It is shown that the destabilizing action of the surfactant vapors is a further indication that surface elasticity forces are the main factor determining stability of wet, dynamic foams. 相似文献
982.
C. Allen Chang Tamar E. Woodhouse Qihui Wu Ceshing Sheu Katherine McManus 《中国化学会会志》1988,35(4):253-260
Substitution-inert metal complexes, [Co(edda)(H2O)2]+, (Co(edda)(en)]+, [Co(edda)(dmen)]+, [Co(en)2-(gly)]2+, [Co(en)2(acac)]2+, and [Co(trien)(gly)]2+ in their nitrate salt solutions are used as eluents in nonsuppressed cation chromatography (where edda = ethylenediamine-N,N′-diacetic acid, en = ethylenediamine, dmen = N,N′-dime-thylethylenediamine, gly = glycine, acac = acetylacetone, and trien = triethylenetetraamine). It is found that all the mono- and di-valent charged complexes can be used to separate alkali and alkaline earth metal cations, respectively. The separations for monovalent cations are sometimes comparable to those using ultrapure HNO3 solutions. However, the divalent Ca2+ and Sr2+ ions cannot be resolved using the metal complex eluents. On the other hand, a selected, direct non-suppressed IC separation of zinc(II) and cadmium(II) ions is demonstrated for the first time using a substitution-inert metal complex eluent and a conductivity detector. Comparisons of these eluents with those reported previously, i. e. HNO3 and ethylenediammonium salt solution are made and explanations are proposed to account for the different selectivities observed where possible. The future development of this technique is also briefly discussed. 相似文献
983.
Summary The distribution equilibria of cationic compounds in reversed-phase chromatographic systems (ion-pair chromatography) have
been studied on the basis of their effect on a detectable mobile phase component. The solid phase was a polystyrene-divinylbenzene
copolymer and the detectable component, a quaternary ammonium ion, 1-methylpyridine. The solutes were mono- and divalent amines
and quaternary ammonium ions.
The cations can be retained by ion-pair adsorption and ion exchange. Expressions for the ion-pair retention of the solutes
and the mobile phase cation (system peak) have been developed assuming Langmuir distribution of ion pairs to a solid phase
with one kind of binding site. The validity of the expressions has been tested by evaluation of ion-pair distribution constants
using non-linear curve fitting techniques. Good agreement for the constants of common ion pairs was obtained from different
kinds of capacity ratio expressions.
Ion exchange retention can appear beside ion-pair retention, and it has been observed in the pH range 1.6–6.1. The effect
depends not only on cations in the mobile phase, but also on the nature of the buffering systems. 相似文献
984.
Summary High pressure liquid chromatographic methods for the determination of diphenylmethane-4,4-diisocyanate (MDI) and toluene diisocyanate (TDI) in chemical products are described. The MDI- and TDI monomers were determined as their urea derivative formed by the reaction with 9-(methyl aminomethyl)-anthracene. Using these methods MDI- and TDI monomer concentrations have been determined in 55 chemical products: sealing waxes, insulating- and adhesive foam, hardener, primer, adhesives and surface coatings. The recovery of both MDI and TDI monomers from various types of chemical product was found to be 92–97%, and the relative standard deviations of the methods was <5% for all types of products. 相似文献
985.
Summary We have investigated to which extent retention data, acquired on single capillary columns, can be used for predicting retention factors in a coupled column system. For this purpose we utilized a model mixture of 18 lipid components with widely different vapor pressures and polarities. The sample was chromatographed on two columns, SB-biphenyl-30 (70% methyl-30% biphenylpolysiloxane) and SB-cyanopropyl-50 (50% methyl-50% cyanopropylsiloxane). Experimental retention factors, acquired in coupled column systems with two columns connected in different order, were thus compared with values calculated from runs on each single column. The agreement between calculated and experimental values generally was better than 5% without any pressure drop correction.To study the possibility of predicting retention behavior in a wide pressure range from a limited number of experiments, we also investigated the relation between solute retention and mobile phase density. We found that all data could be fitted to second order equations, which gives the possibility to optimize the resolution with respect to pressure from a limited number of runs at different pressures. 相似文献
986.
In this work, different extracts from the microalga Spirulina platensis are obtained using pressurized liquid extraction (PLE) and four different solvents (hexane, light petroleum, ethanol and water). Different extraction temperatures (115 and 170 degrees C) were tested using extraction times ranging from 9 to 15 min. The antioxidant activity of the different extracts is determined by means of an in vitro assay using a free radical method. Moreover, a new and fast method is developed using micellar electrokinetic chromatography with diode array detection (MEKC-DAD) to provide a preliminary analysis on the composition of the extracts. This combined application (i.e., in vitro assays plus MEKC-DAD) allowed the fast characterization of the extracts based on their antioxidant activity and the UV-vis spectra of the different compounds found in the extracts. To our knowledge, this work shows for the first time the great possibilities of the combined use of PLE-in vitro assay-MEKC-DAD to investigate natural sources of antioxidants. 相似文献
987.
Guo X Shuang S Wang X Dong C Pan J Aboul-Enein HY 《Biomedical chromatography : BMC》2004,18(8):559-563
The interaction of rutin and venoruton (troxerutin), with alpha-, beta- and gamma-cyclodextrin (CD), hydroxypropyl-beta-cyclodextrin (HP-beta-CD) and methyl-beta-cyclodextrin (M-beta-CD) was investigated by reversed-phase thin layer chromatography on polyamide plates. A mobile phase consisted of NH(4)OH; NH(4)Cl buffer solution containing various CD concentrations (pH = 9.7, 20 degrees C) was used as mobile phase. The equilibrium constants (K(f)) and the retention factor (R(f)) were determined and used to study the inclusion process. The in fluence of CDs on the solubility of rutin and venoruton was characterized by R(M) values and the increasing hydrophilicity of drugs. The results show that the inclusion capacity of cyclodextrins follows the order HP-beta-CD > M-beta-CD > beta-CD > gamma-CD, and rutin is more easily included by the studied cyclodextrins than venoruton. In addition, the thermodynamic parameters (Delta H, Delta S) for the formation of complexes were obtained from the van't Hoff equation, displaying the enthalpy-entropy compensation effect. 相似文献
988.
Feed additives in animal nutrition: Quantification of a new adrenergic drug by hyphenated techniques
《Journal of separation science》2003,26(5):363-368
Zilpaterol, (±)‐trans‐4,5,6,7‐tetrahydro‐7‐hydroxy‐6‐(isopropylamino) imidazo [4,5,1‐jk]‐[1]benzazepin‐2(1H)‐one, is an adrenergic agonist drug licensed in Mexico and South Africa as feed additive for cattle at slaughter age. In contrast, the EU legislative framework prohibits the use of beta‐agonists as growth promoters to produce lean meat. In this study, the compound was quantified as its TMS derivative both by gas chromatography‐mass spectrometry (GC‐MS) with a quadrupole detector (QUADR) and by GC‐MS/MS with an ion trap detector (ITD), in Electron Impact (EI) ionization. Subsequently, an extraction and clean‐up procedure for the identification of Zilpaterol in commercial feeds was set up. Different extraction solvents and matrices were considered for their influence on Zilpaterol yield. The analytical method led to good recoveries and limits of detection and quantification in feeds well below the 5–20 μg/g dose proposed for animal nutrition. 相似文献
989.
Summary An analytical procedure has been developed for simultaneous determination of solvent mixture vapors to enable evaluation of
occupational exposure. To determine the desorption efficiency the volatile components of the solvent mixtures were generated
from a glass tube filled with glass wool. This device is easy to prepare and use. These vapors were then collected in activated
charcoal tubes and analyzed by capillary gas chromatography. The method was tested with a mixture of 22 solvents, including
aliphatic and aromatic hydrocarbons, alcohols, ethers, esters, and ketones, all at low concentrations. All the components
were detected. When a 99∶1 mixture of carbon disulfide-dimethylformamide was used for desorption the efficiency was>75% for
most of the solvents. 相似文献
990.
A method using GC-MS and derivatization with N-(t-butyldimethylsilyl)-N-ethyltrifluoroacetamide (MTBSTFA) was developed for the analysis of 19 chlorophenols compounds in atmospheric samples (gas
and particles). Air sampling was carried out using a Hi-Vol sampler with glass fibre filter and XAD-2 resin at a flow rate
of 60 m3 h−1. The particle and gas phases were collected separately over a period of 4 h. Samples were Soxhlet extracted, evaporated to
dryness under nitrogen and refilled with acetonitrile. 100 mL of these extracts were derivatized with 100 μL of MTBSTFA at
80 °C for 1 h under strong stirring. Sylylated chlorophenols were injected into a GC-MS in splitless mode and quantified as
their TBDMS derivatives in the SIM mode. Mass spectral analysis of the derivatives of the 19 compounds studied indicates that
the spectra are highly specific showing an ion at [M - 57]+ which is useful for structure confirmation or analysis at low levels using selected ion monitoring. Quantification limits
varied between 5 μg L−1 and 10 μg L−1 which correspond to 20 pg m−3 and 40 pg m−3 for 250 m3 of air sampled. This method was successfully applied to atmospheric samples collected simultaneously in winter 2004 in an
urban (Strasbourg) and rural (Erstein) areas in east of France. 相似文献