Resolution compared

The main cost of this enlianced time resolution compared to fluorescence upconversion, however, is the aforementioned problem of time ordering of the photons that arrive from the pump and probe pulses. Wlien the probe pulse either precedes or trails the arrival of the pump pulse by a time interval that is significantly longer than the pulse duration, the action of the probe and pump pulses on the populations resident in the various resonant states is nnambiguous. When the pump and probe pulses temporally overlap in tlie sample, however, all possible time orderings of field-molecule interactions contribute to the response and complicate the interpretation. Double-sided Feymuan diagrams, which provide a pictorial view of the density matrix s time evolution under the action of the laser pulses, can be used to detenuine the various contributions to the sample response [125]. 

Benchtop X-ray energy dispersive analyzer BRA-17-02 based on a gas-filled electroluminescent detector with an x-ray tube excitation and range of the elements to be determined from K (Z=19) to U (Z=92) an electroluminescent detector ensures two times better resolution compared with traditional proportional counters and possesses 20 times greater x-ray efficiency compared with semiconductor detectors. The device is used usually for grits concentration determination when analysing of aviation oils (certified analysis procedures are available) and in mining industry. 

In principle GD-MS is very well suited for analysis of layers, also, and all concepts developed for SNMS (Sect. 3.3) can be used to calculate the concentration-depth profile from the measured intensity-time profile by use of relative or absolute sensitivity factors [3.199]. So far, however, acceptance of this technique is hesitant compared with GD-OES. The main factors limiting wider acceptance are the greater cost of the instrument and the fact that no commercial ion source has yet been optimized for this purpose. The literature therefore contains only preliminary results from analysis of layers obtained with either modified sources of the commercial instrument [3.200, 3.201] or with homebuilt sources coupled to quadrupole [3.199], sector field [3.202], or time-of-flight instruments [3.203]. To summarize, the future success of GD-MS in this field of application strongly depends on the availability of commercial sources with adequate depth resolution comparable with that of GD-OES. 

The selection of the pulse amplitude and potential scan rate usually requires a trade-off among sensitivity, resolution, and speed. For example, larger pulse amplitudes result in larger and broader peaks. Pulse amplitudes of 25-50 mV, coupled with a 5 mV s 1 scan rate, are commonly employed. Irreversible redox systems result in lower and broader current peaks (i.e., inferior sensitivity and resolution) compared with those predicted for reversible systems (6). In addition to improvements in sensitivity and resolution, the technique can provide information about the chemical form in which the analyte appears (oxidation states, complexa-tion, etc.). 

The resolution of an acoustic lens is determined by diffraction limitations, and is 7 = 0.51 /N.A [95], where is the wavelength of sound in liquid, and N.A is the numerical aperture of the acoustic lens. For smaller (high-frequency) lenses, N.A can be about 1, and this would give a resolution of 0.5 Kyj. Thus a well designed lens can obtain a diameter of the focal spot approaching an acoustic wavelength (about 0.4 /Ltm at 2.0 GHz in water). In this case, the acoustic microscope can achieve a resolution comparable to that of the optical microscope. 

To record a 3D spectrum that covers the entire spectral range in all three dimensions with a resolution comparable to that obtained in 2D spectra, an enormous amount of data must be processed, which not only may be beyond tbe storage capabilities of most computer systems, but may... 

HPLC has proved to be fast and sensitive for the analyses of phenolic plant constit-nents, and is especially useful for the analysis of anthocyanins. The first application of HPLC to anthocyanin analyses was in 1975 by Manley and Shubiak and it has now become the method of choice for the separation of mixtures of anthocyanins and anthocyanidins. HPLC is now used for anthocyanin qualitative, quantitative, and preparative work, offering improved resolution compared to chromatographic procedures previously employed. It also allows for simultaneous rapid monitoring of the eluting anthocyanins. ... 

As remarked in the previous section EH is able to retrieve phase and amplitude information separately and with a resolution comparable with that of conventional HREM observations. 

Preparative HPLC of component II was difficult. Component II was collected with a resolution comparable to that shown in Figure 2. Higher resolution showed the presence of at least 5 minor peaks. Slowing the water/methanol gradient finally produced a single peak, which when collected, totaled 14 mg of slightly yellow oil from 2.1 gms OFAs extracted with ODS silica (16). Structural work on II has not yet appeared in the literature, so more detail is included. 

Figure 9.3 shows an impurity separation under conventional pressures with a 5 /mi particle, 2.1 x 150 mm column, and the same separation performed via UPLC using a 2.1 x 50 mm column with 1.7 /im particles. The run time was improved by a factor of six, with overall resolution comparable to that of the original separation on the 5 /an column. The application of UHPLC technology to impurity profile analysis can exert a significant impact on laboratory productivity by achieving a... 

FTIR spectrometers provide a high resolution compared to dispersive instruments. Moreover, this resolution is constant over the full spectral range. 

Hydrodynamic injection was compared with electrokinetic injection (data not shown). The two injection modes gave comparable percent peak areas. Electrokinetic injection gave slightly higher resolution compared to hydrodynamic injection. For the CE-SDS method, electrokinetic injection is generally recommended. 

Lipase, which is highly useful for kinetic resolution, however, has a limitation for use in DKR in that it carmot be used for (S)-configuration products. For this purpose, subtiHsin, a protease from Bacillus licheniformis, can replace lipase since it provides complementary enantioselectivity (Scheme 1.4). Subtilisin, however, has been much less frequently employed in resolution compared to lipase because it displays poor catalytic performance in organic media. Subtilisin is inferior to lipase in several properties such as activity, enantioselectivity and stability. Accordingly, the use of the enzyme usually requires some special treatments for activation and stabilization before use. For example, the treatment of subtilisin with surfactants has enhanced substantially its activity and stability up to a synthetically useful level. 

The support can then be mechanically coated with a variety of liquid stationary phases. The mobile phase most commonly used in packed column GC is nitrogen with a flow rate of ca 20 ml/min. Packed column GC affords a relatively low degree of resolution compared to capillary GC typically 4000-6000 plates for a 2 m column compared to > 100 000 plates for a 25 m capillary column. The high temperature limit of packed columns is ca 280°C beyond this temperature the liquid stationary phase evaporates at a rate which creates a large background signal. However, for many routine quality control operations, they are quite adequate. 

The most important aspect of electron microscopy in solid state chemistry lies in its ability to elucidate problems that are beyond the capability of X-ray or neutron crystallography. High-resolution electron microscopic (HREM) images show local structures of crystals in remarkable detail in Fig. 2.10 we show the HREM image of Big, W03 obtained with the Cambridge University 500 kV microscope to show the improved resolution compared with the image obtained with a 200 kV microscope... 

In general, ion reaction rates can be observed directly in a time-of-flight spectrometer with a time resolution comparable to that of the system, which is about 10-9 to 10 los. The rate measurement can achieve a much better time resolution by using an ion reaction time amplification method. With this method, very fast ion reactions can be measured with a time resolution much better than the time resolution of the system. It is with this method69 that the field dissociation reaction of 4HeRh2+ was measured with a time resolution of about 20 femtoseconds when the time resolution of the system was still only 1 ns. 

The availability of solid-state detectors (such as the charge-coupled detector, CCD) makes it possible to acquire simultaneously significant portions of the spectra or even the entire rich spectra obtained by ICP-OES in the UV-Vis region, thus providing a large amount of data. The commercial availability of ICP-OES instruments with these multichannel detectors has significantly renewed interest in this technique. However, some limitations, such as the degradation of the spectral resolution compared with photomultiplier-based dispersive systems, still remain. 

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