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Step height analysis

The determination of film thicknesses can be carried out, as shown above, by analyzing cross sectional plots. An improved statistics is obtained using a step height analysis. Here, two sets of two lines define certain areas on the two levels of altitude, which are analyzed. Instead of calculating individual height differences, the software estimates the mean difference in height between the areas selected Fig. 2.40. [Pg.65]

Fig. 2.40 Step height analysis of AFM height images of a thin polymer film prior to and after swelling (step heights of 19.0 and 21.3 nm were measured). Reproduced with permission from [31]. Copyright 2005. American Chemical Society... Fig. 2.40 Step height analysis of AFM height images of a thin polymer film prior to and after swelling (step heights of 19.0 and 21.3 nm were measured). Reproduced with permission from [31]. Copyright 2005. American Chemical Society...
The step height analysis of these two-dimensional cholesterol crystals gives 90 A, which corresponds to six layers of cholesterol (90 A/length of cholesterol molecule =15 A). This is different from what is seen for the collapsed films of Mg-(stearate)2, as is well known from monolayer surface pressure vs. area isotherms. ... [Pg.662]

In summary, pulse-height analysis (PHA) prior to a Mossbauer measurement is an essential step in tuning a Mossbauer spectrometer. PHA allows the adjustment of the y-detection system to the Mossbauer photons and the reduction of noise by rejecting nonresonant background radiation. [Pg.37]

It is a well recognized fact that in field ion microscopy field evaporation does not occur at a constant rate because of the atomic step structures of the tip surface. For the sole purpose of a compositional analysis of a sample, one should try to aim the probe hole at a high index plane where the step height is small and field evaporation occurs more uniformly. But even so, the number of atoms field evaporated per HV pulse or laser pulse within the area covered by the probe-hole will not be the same every time. It is reasonable to assume that the field evaporation events are nearly random even though there has been no systematic study of the nature of such field evaporation events. Let the average number of atoms field evaporated per pulse within the area covered by the probe-hole area be n. The probability that n atoms are field evaporated by a pulse is then given by the Poisson distribution... [Pg.156]

In aqueous methanol, indomethacin exhibits a half-wave potential (E.,-) at the droning mercury electrode which is dependent upon pH. In 0.1M methanolic lithium chloride, indomethacin has two waves between -1.4v and -1.6v (vs. S.C.E.). The first step height is diffusion controlled and corresponds to a two electron reduction of the amide carbonyl. The second wave is believed to be a kinetic wave. The method as described is specific for nonhydrolyzed indomethacin and is suitable for analysis of capsules, suppositories and suspensions with precision of +1.2%, +0.7% and +1.2% for the respective formulations(43). [Pg.230]

The major advantage of square-wave voltammetry is its speed. The effective scan rate is given by / AEs. The term / is the square-wave frequency (in Hz) and AEs is the step height. Frequencies of 1-100 cycles per second permit the use of extremely fast potential scan rates. For example, if AEs = 10 mV and /= 50 Hz, then the effective scan rate is 0.5 V/s. As a result, the analysis time is drastically reduced a complete voltammogram can be recorded within a few... [Pg.81]

Fig. 9 Catalytic square wave voltammetry of PDDA/ds-DNA (/Mb/ds-DNA)2 films on rough PG electrodes before and after incubations at 37°C with 2% styrene (no styrene in controls) and 0.2 mM H202 in aerobic buffer (SWY amplitude 25 mV frequency 15 Hz step height 4 mV PDDA=polydiallyldi-methylammonium ion). After incubation, electrodes were washed and placed into pH 5.5 buffer containing 50 pM Ru(bpy)3+ for the SWY analysis. (From Ref. [15] with permission. Copyright American Chemical Society.)... Fig. 9 Catalytic square wave voltammetry of PDDA/ds-DNA (/Mb/ds-DNA)2 films on rough PG electrodes before and after incubations at 37°C with 2% styrene (no styrene in controls) and 0.2 mM H202 in aerobic buffer (SWY amplitude 25 mV frequency 15 Hz step height 4 mV PDDA=polydiallyldi-methylammonium ion). After incubation, electrodes were washed and placed into pH 5.5 buffer containing 50 pM Ru(bpy)3+ for the SWY analysis. (From Ref. [15] with permission. Copyright American Chemical Society.)...
Figures 2b,d represent a detailed analysis of cross sections indicated in figures 2a,c as black solid lines. It is demonstrated that the step heights of the observed features are in good agreement with the value for one monolayer of standing PSP molecules corresponding to 2.6 nm. The formation and increment in size of these crystallites is induced by increasing the substrate temperature dining PSP deposition, which is observed for both - illuminated and non-illuminated substrates -as shown in Figure 1. Similar results are found in literature for small organic molecules [13],... Figures 2b,d represent a detailed analysis of cross sections indicated in figures 2a,c as black solid lines. It is demonstrated that the step heights of the observed features are in good agreement with the value for one monolayer of standing PSP molecules corresponding to 2.6 nm. The formation and increment in size of these crystallites is induced by increasing the substrate temperature dining PSP deposition, which is observed for both - illuminated and non-illuminated substrates -as shown in Figure 1. Similar results are found in literature for small organic molecules [13],...
Only horizontal components of shifts from step to step are considered here. In intensity analysis, however, one must also consider those phase shifts arising from different step heights normal to the surface. [Pg.197]

There is no universal procedure for the qualitative evaluation of the steps in the record the interpretation is mainly based on the comparison of the data obtained by the analysis of standard substances and of the samples under the same conditions. The significance of either agreement or disagreement between the qualitative parameters of the records of the standard mixttire and the sample must be taken into consideration. If a known standard substance provides a step which does not coincide with any step height of the sample, then it can be stated that the standard substance is not present in the sample. If the step height of the standard coincides with one of the steps of the sample, the presence of a substance identical with the standard substance in the sample can be considered as probable only. [Pg.151]

For qualitative analysis, it is necessary to take into account in the first place the fact that the heating in various zones is different and step heights h,j and h correspond to reciprocal mobilities % and Uj of not only different substances X and S but also to various temperatures of the zones, and Tg. These also differ from the thermostat temperature, T, i.e. qualitative index Ax(S) represents the ratio (cf. Eq. (28))... [Pg.156]

The amount of data to be handled during this evaluation procedure requires the use of computers. At present, the multichannel analyzer not only carries out pulse height analysis but also does most of the data processing. The manufacturers of computer-based MCAs usually provide built-in or software programs for the different aforementioned steps. [Pg.776]


See other pages where Step height analysis is mentioned: [Pg.65]    [Pg.229]    [Pg.666]    [Pg.359]    [Pg.65]    [Pg.229]    [Pg.666]    [Pg.359]    [Pg.1931]    [Pg.76]    [Pg.73]    [Pg.120]    [Pg.121]    [Pg.89]    [Pg.25]    [Pg.13]    [Pg.101]    [Pg.20]    [Pg.458]    [Pg.317]    [Pg.14]    [Pg.125]    [Pg.665]    [Pg.514]    [Pg.115]    [Pg.661]    [Pg.665]    [Pg.30]    [Pg.1931]    [Pg.73]    [Pg.245]    [Pg.186]    [Pg.955]    [Pg.1997]    [Pg.399]    [Pg.45]    [Pg.1429]    [Pg.209]    [Pg.303]   
See also in sourсe #XX -- [ Pg.65 , Pg.229 ]




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