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Samples unconventional

This section deals briefly with classical methods based on conventional mixing of the sample and reagents such as the batch mode and low-pressure flow mixing methods, as well as the use of CL detection in continuous separation techniques such as liquid chromatography and capillary electrophoresis for comparison with the unconventional mixing mode. [Pg.180]

Even at the level of mean field approximation (MFA), the GL theory gives significant information such as penetration depth (l) and coherence length ( ) of the superconducting samples. Many unconventional properties of superconductivity connected with the break down of the simple MFA has been studied both analytically (Tesanovich, 1999)... [Pg.300]

Abstract The discovery in the 1960s to early 1970s that rock geochemistry could be used to detect mineral deposits under 50-100 metres of post-mineralization rocks was probably one of the first indications that that geochemistry could be used for deep exploration. Some case histories from Cyprus and Canada are presented to illustrate this. The second important impetus to considering deep exploration was research into the mechanisms involved in the formation of anomalies. This led to the proposal of electrochemical models and the measurement of unconventional parameters such as pH, conductivity in water slurries of samples as well as measurement of elements in dilute leaches including water. These developments are illustrated by case histories from Canada and Australia. [Pg.47]

For example, our preliminary MALDI MS studies employed a somewhat unconventional sample preparation approach in which the protein deposition step preceded the matrix deposition step. (In the conventional approach, the protein is co-deposited with the MALDI matrix solution.). .. Thus, in the first/next/colleclively group of experiments, we will explore different sample preparation methods to determine if other protocols also lead to an inverse relationship between surface-protein binding affinity and the MALDI ion signal. [Pg.462]

The unconventional applications of SEC usually produce estimated values of various characteristics, which are valuable for further analyses. These embrace assessment of theta conditions for given polymer (mixed solvent-eluent composition and temperature Section 16.2.2), second virial coefficients A2 [109], coefficients of preferential solvation of macromolecules in mixed solvents (eluents) [40], as well as estimation of pore size distribution within porous bodies (inverse SEC) [136-140] and rates of diffusion of macromolecules within porous bodies. Some semiquantitative information on polymer samples can be obtained from the SEC results indirectly, for example, the assessment of the polymer stereoregularity from the stability of macromolecular aggregates (PVC [140]), of the segment lengths in polymer crystallites after their controlled partial degradation [141], and of the enthalpic interactions between unlike polymers in solution (in eluent) [142], as well as between polymer and column packing [123,143]. [Pg.474]

Pathogens and Toxins Risk Minimizing and Prevention by IPCR of Unconventional Sample Matrices... [Pg.278]

In the twelfth official proficiency test, one laboratory failed to identify BHESO in the organic liquid sample because of unconventional sample preparation. The concentrated extract was silylated with BSTFA at room temperature rather than at the recommended 60 °C. [Pg.178]

A quite unconventional approach to internal fission-event detection was a device called the spinner. It operates on the same principle as the cloud chamber. The instrument, Figure 7, consists of a glass cylinder with glass arms filled with about one liter of the sample solution. Upon rotation, a negative pressure develops in the solution through the action of centrifugal forces. The solvent does not evaporate, however, but remains in a metastable... [Pg.299]

In a condensed retrospective as presented here, the exploratory period of superheavy element research may appear as a sequence of frustrating failures. But for the participants it was an exciting time, with a broad range of approaches, from systematic scanning of large numbers of samples to quite unconventional experiments. Claims for success were raised from time to time and challenged for better experiments to prove them. Although in all cases the claims could not be substantiated, they forced the researchers to push physical and chemical detection techniques to levels not achieved before. [Pg.312]

SFG spectroscopy of CO adsorbed on Si02-supported platinum nanoparticle arrays (with 30-, 40-, 45-, 200-, and 1000-nm mean particle diameters), evaporated platinum nanoparticles (6-nm mean diameter), and a thin platinum film (all at approximately 1 bar) was reported by Baldelli et al (132). Unfortunately, the EBL samples had to be prepared under nonUFlV conditions and were cleaned by a rather unconventional method (treated with concentrated FtN03/Fl2S04 solution. [Pg.207]

The presence of carboxylic groups, introduced by maleic anhydride, allows modified HTI to cross-link with unconventional agents, e. g. polyvalent metal oxides, hydroxides, polyamines. For instance, a sample of HTI, completely reacted with maleic anhydride, has been cured with ZnO at 153 °C for 20 minutes and o %d interestii tensile properties. Furthermore, the dynamic-mechanical spectra (Fig. 29)... [Pg.57]

Inoue T, Seta S, Goldberger BA. Analysis of drugs in unconventional samples. In Liu RH, Goldberger BA eds. Handbook of Workplace Drug Testing. Washington, DC AACC Press, 1995 131-58. [Pg.1359]

To omit unconventional instrumentation that was not suitable for routine analysis, as proposed by De Graeve et al.88, Bellia et al.81 developed a quite simple method to determine papaverine in blood samples, using conventional flame ionization or a nitrogen-phosphorus detector. The internal standard, strychnine, was added to the sample prior to extraction, which was carried out with toluene after basification, back extraction with acetic acid and extraction of the liberated base with diethyl ether. The gas chromatography was done on a packed column with 2 % 0V-101 at 275°C. To minimize the adsorption effects, the column was silanized by in situ injection and by injection of a concentrated solution of papaverine and the internal standard prior to routine analysis. Precision and accuracy of the method is shown in Table 14.13. [Pg.128]


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See also in sourсe #XX -- [ Pg.920 ]




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