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Equilibrium Time (equilibrium + time)
Selected AbstractsUltrasound-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] A novel HS-SBSE system coupled with gas chromatography and mass spectrometry for the analysis of organochlorine pesticides in water samplesJOURNAL OF SEPARATION SCIENCE, JSS, Issue 20 2008Paula Grossi Abstract A methodology to analyze organochlorine pesticides (OCPs) in water samples has been accomplished by using headspace stir bar sorptive extraction (HS-SBSE). The bars were in house coated with a thick film of PDMS in order to properly work in the headspace mode. Sampling was done by a novel HS-SBSE system whereas the analysis was performed by capillary GC coupled mass spectrometric detection (HS-SBSE-GC-MS). The extraction optimization, using different experimental parameters has been established by a standard equilibrium time of 120 min at 85°C. A mixture of ACN/toluene as back extraction solvent promoted a good performance to remove the OCPs sorbed in the bar. Reproducibility between 2.1 and 14.8% and linearity between 0.96 and 1.0 were obtained for pesticides spiked in a linear range between 5 and 17 ng/g in water samples during the bar evaluation. [source] Quantitative analogue flume-model study of river,shelf systems: principles and verification exemplified by the Late Quaternary Colorado river,delta evolutionBASIN RESEARCH, Issue 3 2001M. W. I. M. Van Heijst ABSTRACT Physical modelling of clastic sedimentary systems over geological time spans has to resort to analogue modelling since full scaling cannot be achieved within the spatial and temporal restrictions that are imposed by a laboratory set-up. Such analogue models are suitable for systematic investigation of a sedimentary system's sensitivity to allocyclic changes by isolating governing parameters. Until now, analogue models of landscape evolution were mainly qualitative in nature. In this paper, we present a quantitative approach. The quantitative experimental results are verified and discussed by comparison with high-resolution data from the Colorado river,shelf system of the Texas shelf that we used as a prototype. The model's dimensions are proportionally scaled to the prototype, except for a vertical exaggeration. Time is scaled using a Basin Response factor to maintain a similar ratio between the period of change and the system's equilibrium time for model and prototype. A Basin Fill factor was used to compare the ratio between the time-averaged sedimentation rate and the rate of change in accommodation space of model and prototype. The flume-model results are in the form of sediment budgets that are related to shelf cannibalism and fluvial supply, which are compared with the ancestral Colorado river,delta evolution of the last 40 kyr. Model and prototype have similarities in delta evolution in response to one cycle of sea-level change. With sea-level change as the isolated variable, the flume model generates a significant supply pulse caused by headward erosion of the shelf in response to the sea-level fall. This pulse adds to the yield of the hinterland. The supply induced by sea-level change persists during the early rise, although its rate declines. A similar trend is observed on the east Texas shelf. We argue that shelfal and fluvial degradation cycles induced by sea-level changes can significantly influence the timing and amount of sediment supply to basins and must therefore be taken into consideration. [source] Effect of Sodium Halide on Dynamic Surface Tension of a Cationic SurfactantCHINESE JOURNAL OF CHEMISTRY, Issue 8 2005Lü Feng-Feng Abstract The equilibrium and dynamic surface tension (DST) of the novel cationic surfactant, 3-(p -nonylphenoxy)-2-hydroxylpropyl trimethyl ammonium bromide, abbreviated as RTAB, were studied. The effect of sodium halide such as NaCl, NaBr and NaI on the DST behavior of the RTAB solution below its CMC was studied in detail. Due to the preferential adsorption, the effect of hydration and salting out, the ability to reduce the DST values at the same concentration was in the order of NaI>NaBr>NaCl. Attributed to its high surface activity, the equilibrium time of the DST of the surfactant solution was insensitive to the ionic strength. [source] Field testing of equilibrium passive samplers to determine freely dissolved native polycyclic aromatic hydrocarbon concentrationsENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 3 2008Gerard Cornelissen Abstract Equilibrium passive samplers are promising tools to determine freely dissolved aqueous concentrations (CW,free) of hydrophobic organic compounds. Their use in the field, however, remains a challenge. In the present study on native polycyclic aromatic hydrocarbons (PAHs) in Oslo Harbor, Norway, two different passive sampler materials, polyoxymethylene (POM; thickness, 55 ,m [POM-55] and 500 ,m [POM-500]) and polydimethylsiloxane (PDMS; thickness, 200 ,m), were used to determine in the laboratory CW,free in sediment pore water (CPW,free), and the suitability of five passive samplers for determination of CW,free in overlying surface water was tested under field conditions. For laboratory determinations of CPW,free, both POM-55 and PDMS turned out to be suitable. In the field, the shortest equilibrium times (approximately one month) were observed for POM-55 and PDMS (thickness, 28 ,m) coatings on solid-phase microextraction fibers, with PDMS tubing as a good alternative. Low-density polyethylene (thickness, 100 ,m) and POM-500 did not reach equilibrium within 119 d in the field. Realistic values were obtained for dissolved organic carbon,water partition coefficients in the field (approximately one log unit under log KOW), which strengthened the conclusion that equilibrium was established in field-exposed passive samplers. At all four stations, chemical activity ratios between pore water and overlying water were greater than one for all PAHs, indicating that the sediment was a PAH diffusion source and that sediment remediation may be an appropriate treatment for PAH contamination in Oslo Harbor. [source] | ||||||||||