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Experimental sequence

The basis for FTMS is ion-cyclotron motion. A simple experimental sequence in FTMS is composed of four events quench, ion formation, excitation and ion detection. Ions are created in or injected into a cubic cell where they are held by an electric trapping potential and a constant magnetic field B. Each ion assumes... [Pg.395]

Figure 17-2 Typical results for two possible experimental sequences. Figure 17-2 Typical results for two possible experimental sequences.
Fig. 8.20 Experimental sequence of surface sensing (a) The sensor surfaces are functionalized with biotinylated BSA (b) Streptavidin is specifically bound to the sensor surface with the biotin moiety (c) Biotin is captured on the sensor surfaces by the streptavidin... Fig. 8.20 Experimental sequence of surface sensing (a) The sensor surfaces are functionalized with biotinylated BSA (b) Streptavidin is specifically bound to the sensor surface with the biotin moiety (c) Biotin is captured on the sensor surfaces by the streptavidin...
Assay of Homogenate for Aldrin Epoxidation. The following experimental sequence was designed to determine the optimum in vitro conditions for aldrin epoxidation in larval whole body homogenates 1) the effect of component chemicals generally included in an incubation mixture, 2) a pH profile, 3) a temperature profile, 4) a molarity profile, 5) a reaction time profile, 6) a larval concentration (enzyme concentration) profile, 7) a substrate concentration profile, and 8) a restudy of the effects of component chemicals in the initial incubation mixture (Step 1) upon aldrin epoxidation under optimum conditions as defined by steps 2-7 above. The effect of PBO, FMN, and FAD upon enzyme activity was also tested. [Pg.352]

X 10 2 M Tris HC1 buffer, pH 7.5, 2.4 X 10 3 M glucose 6-phosphate (G-6-P), 1.6 units glucose 6-phosphate dehydrogenase (G-6-P dH), 5.1 X 10"5 M NADP, and 2.7 X 10 3 M KC1. In addition, the following chemicals were included in the final concentration indicated 5.1 X 10-3 M NADH, 1% (W/V) bovine serum albumin (BSA), and 1.0 mg aldrin in 0.1 ml ethanol. Whole body homogenate experiments included all of the above chemicals unless otherwise noted. Reaction mixtures were incubated with swirling in test tubes at 30 - 1°C. Reactions in Steps 1-4 of the experimental sequence were stopped after 1 hr and Steps 6-8 after 15 min, by the addition of 2 ml 5% TCA. [Pg.352]

FIGURE 10 Example of an experimental sequence for holistic PQ validation on an HPLC... [Pg.328]

Phloroisobutyrophenone is unstable when heated in the presence of acid the addition of Rochelle salt prevents the precipitation of aluminium hydroxide when the free acid is neutralised with sodium hydroxide. If any precipitate does appear more Rochelle salt should be added the exact amount of aqueous sodium hydroxide will vary with each experimental sequence the point of neutrality is ascertained with universal indicator paper. [Pg.1011]

Single Resonance Experimental sequence using ion formation and... [Pg.197]

Fig. 11.1. Cyclic Voltammetry on Pt electrodes in 1.0 M H2S04. Voltage scan rate, vs = 100 mV s-1. Variation of potential of positive scan reversal basic curve curve in the presence of 11WEPN. Voltages of scan reversal UH (1) 1.4 V, (2) 1.6 V, (3) 1.7 V. Shown is the sixth cycle after starting the experimental sequence. Freshly prepared Pt electrode for the first sequence was at the most positive potential of scan reversal. T = 20 °C, N2 purging. (Reprinted from B. Wermeckes and F. Beck, Electrochim. >4cfa30 1491, copyright 1985, with permission from Elsevier Science.)... Fig. 11.1. Cyclic Voltammetry on Pt electrodes in 1.0 M H2S04. Voltage scan rate, vs = 100 mV s-1. Variation of potential of positive scan reversal basic curve curve in the presence of 11WEPN. Voltages of scan reversal UH (1) 1.4 V, (2) 1.6 V, (3) 1.7 V. Shown is the sixth cycle after starting the experimental sequence. Freshly prepared Pt electrode for the first sequence was at the most positive potential of scan reversal. T = 20 °C, N2 purging. (Reprinted from B. Wermeckes and F. Beck, Electrochim. >4cfa30 1491, copyright 1985, with permission from Elsevier Science.)...
A bare platinum electrode was coated with a close-packed monolayer of n-octadecylamine by retraction from the molten crystal compound (2). The contact angle of methylene iodide with the monolayer was 68° to 70°, which should be true if the film was close packed. This film-coated electrode was used with the FEP resin-covered gold electrode in the experimental sequence described... [Pg.110]

What about an hypothetical experiment yielding a non-Poisson distribution of light-on and light-off states On the basis of the results of Section XV.E, we are led to believe that it would be impossible to make the rate of Gibbs entropy increase to coincide with the KS entropy. We are convinced that for the same reasons the results of the work of Ref. 139 could not be extended to this case, and it would be impossible, in conclusion, to establish a connection between the rate of von Neumann entropy increase and the KS of the experimental sequence of light-on and ligh-off states. [Pg.451]

Though we can compare electron densities directly, there is often a need for more condensed information. The missing link in the experimental sequence are the steps from the electron density to the one-particle density matrix f(1,1 ) to the wavefunction. Essentially the difficulty is that the wavefunction is a function of the 3n space coordinates of the electrons (and the n spin coordinates), while the electron density is only a three-dimensional function. Drastic assumptions must be introduced, such as the description of the molecular orbitals by a limited basis set, and the representation of the density by a single Slater-determinant, in which case the idempotency constraint reduces the number of unknowns... [Pg.40]

In the experimental sequence, the authors at this point replace methylene chloride by THF (tetrahydrofuran) and the mixture is exposed to a mild ba.se in a two-phase system. The three carbonyl groups of V should all be reactive towards nucleophilic bases such as hydroxide ion, but they also differ remarkably in their susceptibility. Of the three, the keto function would be expected to be more prone to react as a consequence of dipole-dipole interactions with its vicinal ester grouping. The intermediate ketone hydrate anion VI may in principle trigger the disconnection of the three bonds around the central carbon as follows ... [Pg.193]

As indicated in Table 5.3d, significant negative enthalpies and entropies of exchange for the exchange of halide ions on quaternary ammonium resins could be interpreted in terms of pure electrostatic interactions. However such a coulombic model invoking solvated ion size or distance of closest approach fails to conform to the observed affinity order I > Br > CI > F . If one includes a larger polyatomic anion such as perchlorate, Cl 04 the experimental sequence is Cl 04 > I > Br"> Cr > F" which clearly contradicts any simple coulombic attraction theory. [Pg.128]

An additional probe of the system is the spin label that we have examined by using ESR. The experimental sequence employed is shown in Figure 4. It is well known that coals contain significant amounts of kinetically stable carbon radicals, which yield an ESR spectrum of the type shown in Figure 4(a). In this particular sample of Wyodak coal, weighing about 200 mg, 3.6 x 10 spins were observed. Immediately after, a hexane solution containing the spin label TEMPOL (2,2,6,6-... [Pg.29]

A script language based on simple text files facilitated the user to predefining complex experimental sequences to be performed by the electrochemical robotic system. This allows executing of complex experimental sequences without actually knowing the programming code. Available action modules consist of a word built by the x,y-position, the name of the procedure, and all necessary parameters that are used by the procedure. A list of action modules, which can be easily extended... [Pg.344]

Table 14.2 Action modules and list of parameters which are transferred from the script file to the individual program modules for the different experimental sequences... Table 14.2 Action modules and list of parameters which are transferred from the script file to the individual program modules for the different experimental sequences...
The data of Table 6.7 show that at pH = 1, in the area of low HF concentrations, the complex formation in group 6 has a reversed trend, W > Sg > Mo, while in the area of high HF concentrations, Sg follows the trend found for Mo and W, so that Sg > W > Mo. The obtained sequences for Mo and W agree with the experimental sequence in the values of K for the sorption of Mo and W from HF solutions by an anion exchange resin (Caletka and Krivan 1990). Thus, Sg will be extracted below or above W depending on the HF concentrations. Considerations of further reactions at much lower HF concentrations with formation of the M(>3F and M02F2(H20)2 complexes of Mo, W and Sg are in progress. [Pg.240]

The second and third bands show a relative decrease in intensity in the He(II) spectrum and are assigned to the M.O. correlating with 7t2 and tt, respectively. The 7t2 band shows a smaller intensity reduction in the He(II) spectrum than the n1 band, which is taken to indicate significant metal character for 7T2. Variations in the profile of the first band also produce evidence that one of its composite ionizations possesses significant ligand character. Ab initio calculations indicate substantial orbital relaxation on ionization, but do not reproduce the experimental sequence of bands. [Pg.93]

The cause of the deviation of the experimental sequence from the theoretical one has not been sought in experimental errors or inaccuracies it was beautifully confirmed by Otaki s experiments (44), who reported the following ratio of decomposition rates r (90% deute-rated complexes on reduced Ag at 100°C) ... [Pg.58]


See other pages where Experimental sequence is mentioned: [Pg.528]    [Pg.757]    [Pg.396]    [Pg.148]    [Pg.79]    [Pg.187]    [Pg.68]    [Pg.190]    [Pg.64]    [Pg.379]    [Pg.451]    [Pg.247]    [Pg.40]    [Pg.38]    [Pg.259]    [Pg.346]    [Pg.128]    [Pg.135]    [Pg.136]    [Pg.137]    [Pg.137]    [Pg.60]    [Pg.254]    [Pg.369]    [Pg.203]   
See also in sourсe #XX -- [ Pg.178 ]




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