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Previous extraction studies

Analysis of pesticides in water was performed by fully automated online solid-phase extraction-liquid chromatography-tandem mass spectrometry (SPE-LC-MS/ MS) [25, 31]. These pesticides (a total of 22 belonging to the classes of triazines, OP, chloroacetanilides, phenylureas, thiocarbamates, acid herbicides, and anilides) were selected on the basis of previously published studies [20, 25], information gathered from the water authorities, and known use in rice crops. [Pg.264]

Halides other than fluoride form very weak complexes in aqueous solution there are no reliable equilibrium constants to be found in the literature. The solution chemistry of aqueous solutions of beryllium chloride, bromide, and iodide have been reviewed previously (9). Some evidence for the formation of thiocyanate complexes was obtained in solvent extraction studies (134). [Pg.136]

From the previously discussed studies, the oxidative burst response appears to integrate and/or orchestrate several defense responses. These provide an adaptive mechanism to counteract attacks on or injury to algal cells and thalli. As shown in Fig. 12.2, the occurrence of an oxidative burst associated with the perception of cell-free extracts of A. operculata was shown to play a crucial role in the natural resistance of C. crispus gametophytes (Bouarab et al. 1999). [Pg.259]

Table I presents an evaluation of Equation 21 based on previously reported values for log Kqw, V, and 6. The constant Cj was calculated from the log KQC of benzene estimated from Figure 2. Estimates of log KQC for the remaining compounds in Table I are presented for 6 equal to 10.3 and 11.5. The value of 10.3 corresponds to the 5p implied from solvent extraction studies (31). In this case,... Table I presents an evaluation of Equation 21 based on previously reported values for log Kqw, V, and 6. The constant Cj was calculated from the log KQC of benzene estimated from Figure 2. Estimates of log KQC for the remaining compounds in Table I are presented for 6 equal to 10.3 and 11.5. The value of 10.3 corresponds to the 5p implied from solvent extraction studies (31). In this case,...
We began the batch squalane extraction studies by mixing 30 mis of the middle phase from the surfactant system 10% SDBS/17% IPA/12.4% NaCl/dodecane (Figure 6) with 30 mis. of squalane. The solutions were mixed for 10 minutes on a wrist action shaker and allowed to separate. Coalescence was rapid and complete in 5 minutes. The squalane rich phase was separated, and both phases were analyzed for dodecane and SDBS by the methods described previously. These results are summarized in Table V. The batch study was encouraging since 98% of the original solubilized dodecane from Figure 6 (12.4% NaCl ) partitioned into squalane. All the surfactant remained in the aqueous phase, as expected. [Pg.264]

Liquid-liquid extraction (LLE), solid phase extraction (SPE), and solid phase micro-extraction (SPME) are frequently applied for sample pretreatment. The type of extraction is highly related to the type of metabolites selected for determination. In previous metabolomics studies, extraction was focused on compounds of adequate stability that could be extracted together (carbohydrates, esters, amino acids, or organic acids). [Pg.244]

As indicated before, previous detailed studies of particulate formation and emission processes in automobile engines and exhaust systems have been done using probes which extracted a (hopefully) representative sample of the exhaust gas that was subsequently analyzed for various particulate properties (5). Similar techniques have been used in the most recently developed systems to measure the amounts of particles emitted from auto exhaust. Such sampling techniques, however, suflFer from inherent disadvantages in that they interfere with the hot flow particulate processes and have an unknown effect on the particulates as they flow through the system to an exterior point of analysis. This problem can also be compounded by several phenomena anisokinetic sampling, deposition of particulates in the sampling system, or condensation caused by temperature drops. [Pg.200]

Recognizing the need for a more uniform, polysaccharide material for detailed constitutional studies, O Dwyer prepared two hemicellulose fractions from beechwood previously extracted with water and 0.2% sodium hydroxide. As in previous work, the hemicelluloses were extracted from beechwood sawdust with 4% aqueous sodium hydroxide. Pectic materials were precipitated with lime-water, and a fraction designated hemicellu-lose-A was obtained by acidifying the solution with acetic acid. To the filtrate, from hemicellulose-A, was added 95 % ethanol to precipitate hemi-cellulose-B. After further purification, both of these hemicelluloses were subjected to chemical study. Hemicellulose-A ([ccjn —107° in 1 % sodium hydroxide) was observed to be soluble in cold water when freshly prepared, but it was insoluble after being dried. The preparation did not reduce... [Pg.300]

The extraction of by a synergistic mixture of 2-thenoyltrifluoroacetone (HTTA) and tributylphosphate (TBP) from nitric acid media into benzene has been studied. Previous literature reports have described the synergistically extracted species as U02(N03)(TTA) TBP. However, Patil et have used extraction studies to show that the nitrate anion is not present in the extracted complex. Rather, the only species involved in the synergistic extraction is UO2-(TTA)2 TBP. ... [Pg.298]

Capella-Peiro et al. (28) used a 3 full factorial design to optimize the capillary zone electrophoresis (CZE) separation of a group of seven antihistamines (brompheniramine, chlorpheniramine, cyproheptadine, diphenhydramine, doxylamine, hydroxyzine, and loratadine). In this case, critical parameters such as pH (a concentration of 20 mM phosphate was kept constant in all the experiments) and the applied voltage were studied to evaluate their effect on the resolution and efficiency. Maximum response was achieved at pH 2.0 and an applied voltage of 5 kV. After a repeatability study to check the precision of the electrophoretic method, as well as a suitable calibration, the usefulness of this optimized method was demonstrated through the determination of the listed histamines in pharmaceuticals, urine, and serum samples (recoveries were in agreement with the stated contents). Urine samples were diluted and directly injected in the CE system, while serum samples were previously extracted by means of a solid-phase extraction (SPE) procedure. [Pg.136]

We have certainly noticed in the previous discussion on the gadolinium break that the formation constants are not a simple function of the atomic numbers, and that the plots of the thermodynamic quantities (Fig. 3, 5) leave room for further subdivision of the diad series of Klemm. Actually Peppard etal. (41) during their long time involvement in the liquid-liquid extraction studies of the lanthanides and the actinides (41 —43) observed that the diad series of Klemm could be further subdivided into two subgroups each, giving rise to what they termed as a tetrad series. They summarized (43) their findings as ... [Pg.12]

Solvent Extraction Studies. Techniques necessary to detect lipid species extracted from in vitro and in vivo exposed Biomer were developed. Extractions with a nonpolar swelling solvent (e.g., CHC13) employing a soxhlet apparatus were performed to extract preferentially lipophilic biological components from Biomer or previously isolated neointimal samples. Experimentation demonstrated the high solubility in chloroform of polymer-derived monomeric and oligomeric components. A separation of lipids from these components was therefore required. [Pg.396]

Continuing the theme of comprehensive studies, Woessner [23] recently carried out another major investigation of clay structure. The main improvement here is the use of high-speed MAS. Some of the spectra were collected at 9 kHz, which was significantly faster than for most spectra of clays published to that point. Several of the conclusions reached are in agreement with previous structural studies. One additional parameter that was extracted was the SOQE (second-order quadrupole effect), which is simply the isotropic part of the second-order quadrupolar interaction. The QCC (quadrupolar coupling constant) and T] (asymmetry parameter) are defined in this paper as follows... [Pg.318]

The natural consequence of lead extraction procedures is the need for a subsequent device reimplantation. For this reason, when an extraction procedure is planned, the patient should be aware of the potential risks and complications related to both procedures and should be informed of potential alternatives in case of transvenous reimplantation failure. Reimplantation is not necessary in all the patients. The need for reimplantation after lead extraction cannot be always predicted before pac-ing/defibrillating system removal. In previous published studies, reimplantation rate has been reported to vary from 48% to 87% of cases [1-3] in our experience, according with other centers, reimplantation of a new device is usually not required in about 20% of patients [4, 5]. However, in all patients undergoing lead extraction, especially in case of previous infection, the ongoing need of a cardiac device should be reassessed [6]. [Pg.137]


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