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Gradient samples

To use the DCI probe, 1-2 xL of the sample (in solution) are applied to the probe tip, composed of a small platinum coil, and after the solvent has been allowed to evaporate at room temperature, the probe is inserted into the source. DCI probes have the capability of very fast temperature ramping from 20 to 700 °C over several seconds, in order to volatilise the sample before it thermally decomposes. With slower temperature gradients, samples containing a mixture of components can be fractionally desorbed. The temperature ramp can be reproduced accurately. It is important to use as volatile a solvent as possible, so as to minimise the time required to wait for solvent evaporation, which leaves a thin layer of sample covering the coil. The observed spectrum is likely to be the superposition of various phenomena evaporation of the sample with rapid ionisation direct ionisation on the filament surface direct desorption of ions and, at higher temperature, pyrolysis followed by ionisation. [Pg.364]

When we talk about optimization of serial LC/MS operations, we consider the genuinely serial sequences of actions necessary to perform such analyses including equilibration of columns, sample aspiration, sample injection, isocratic or solvent gradient sample separation, detection, and column washout. [Pg.96]

Hardness was estimated by Vickers indentation on sintered gradient samples, thermal expansion coefficient measurements and elastic behaviour was tested on the different dispersions. Preliminary mechanical testing (single edge notched beam, 3PB-SENB) and oxidation tests were performed on sintered FGM s. [Pg.351]

Figure 6b. Analytical separations of a crude glycopeptide complex (gradient). Sample crude antibiotic extract. Column Beckman Ultrasphere ODS, 5 pirn, 4.6 x 150 inm. Mobile phase 27 to 37% acetonitrile in 0.1 M KH2PO4PH 3.2. Flow 1.5 ml/min. Detection 220 nm. Figure 6b. Analytical separations of a crude glycopeptide complex (gradient). Sample crude antibiotic extract. Column Beckman Ultrasphere ODS, 5 pirn, 4.6 x 150 inm. Mobile phase 27 to 37% acetonitrile in 0.1 M KH2PO4PH 3.2. Flow 1.5 ml/min. Detection 220 nm.
It is found that the abrasion value is minimal at a side of the gradient sample contained from PU only or its content is greater in relation to the PIC component, and obtains the values typical of standard rubbers [3], As PIC concentration in the rigid part increases, the abrasion value also increases to significant values (6-7-10 3 cm3/m). It is found that the abrasion value also is affected the technical carbon trademark. As the trademark P803 is used, the abrasion index is insignificantly lower compared with K354 trademark use. [Pg.163]

Lyotrope gradient samples ideally should be fluid. [Pg.103]

Clearly, the best solution is to utilize the entire echo signal and Fourier transform it. Then, you would have the field distribution itself and it can be examined for any distortions due to non-uniform field gradient, sample tilting (except... [Pg.212]

Normal phase separation using a gradient (sample as in Fig. 4.3k (ii))... [Pg.232]

Novalac resins made from p-cresol condensation with formaldehyde were characterized on a 50°C C,g column (A = 280nm) using a complex 55-min 0/50/50 50/50/0 THF/methanol/water gradient. Samples were made up as... [Pg.297]

Figure 1. Gold substrates immersed in either CHsICHgliiSH-or HO(CH2)iiSH-containing ethanol solutions. Static contact angles were measured after different immersion times. The lower the concentration of the solutions, the longer it takes to reach the saturation values. For comparison, two gradient samples are also shown the gradient sample was prepared by immersing a gold-coated substrate (4 cm in length) in 0.003 mM CH3(CH2)iiSH solution at a speed of 40 pxa/s by means of a linear-motion drive. Figure 1. Gold substrates immersed in either CHsICHgliiSH-or HO(CH2)iiSH-containing ethanol solutions. Static contact angles were measured after different immersion times. The lower the concentration of the solutions, the longer it takes to reach the saturation values. For comparison, two gradient samples are also shown the gradient sample was prepared by immersing a gold-coated substrate (4 cm in length) in 0.003 mM CH3(CH2)iiSH solution at a speed of 40 pxa/s by means of a linear-motion drive.
We have shown elsewhere by polarization-modulation infrared spectroscopy (PM-IRRAS) that gradient samples prepared by the two-step method exhibit a highly ordered structure along the gradient and do not show noticeable differences when compared... [Pg.481]

Contact-Angle Measurements. Static contact angles were measured at room temperature and ambient humidity. On gradient samples, a single measurement of sessile drops was... [Pg.535]


See other pages where Gradient samples is mentioned: [Pg.232]    [Pg.321]    [Pg.67]    [Pg.69]    [Pg.73]    [Pg.82]    [Pg.204]    [Pg.187]    [Pg.137]    [Pg.496]    [Pg.120]    [Pg.350]    [Pg.350]    [Pg.385]    [Pg.296]    [Pg.286]    [Pg.643]    [Pg.584]    [Pg.318]    [Pg.143]    [Pg.871]    [Pg.237]    [Pg.238]    [Pg.326]    [Pg.231]    [Pg.87]    [Pg.87]    [Pg.88]    [Pg.88]    [Pg.480]    [Pg.481]    [Pg.489]    [Pg.498]    [Pg.512]    [Pg.536]    [Pg.536]    [Pg.536]    [Pg.536]    [Pg.536]   
See also in sourсe #XX -- [ Pg.165 ]




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