Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Single concentrations

Figure 10-4F(1). Single concentric corrugated tube in single corrugated shell. (Used by permission APV Heat Transfer Technologies.)... Figure 10-4F(1). Single concentric corrugated tube in single corrugated shell. (Used by permission APV Heat Transfer Technologies.)...
Antagonists can produce varying combinations of dextral displacement and depression of maxima of agonist dose-response curves. The concentration-related effect of an antagonist on the system response to a single concentration of agonist constitutes what will be referred to as an inhibition curve. One of the most straightforward examples... [Pg.210]

Yr is the projection of a single concentration data point onto the fh concentration factor. [Pg.136]

REACTIONS THAT ARE ZEROTH-ORDER OR A FRACTIONAL ORDER WITH RESPECT TO A SINGLE CONCENTRATION... [Pg.28]

REACTIONS WITH A COMPLEX DEPENDENCE ON A SINGLE CONCENTRATION VARIABLE... [Pg.34]

In the computer simulations It was necessary to study reaction sequences more complex than those studied by Barkelew, which consequently led to rate functions having double rather than single concentration dependence. Numerous results from both theoretical and computational analyses. Including the effects of e and Tr, have been described elsewhere (see especially Figure 8 of reference 1). [Pg.27]

This result assumes constant density and is most useful when the reaction rate depends on a single concentration, SS-a = A(ciout)-... [Pg.24]

Frequently occurs that extrapolations do not have a common value at their origin ordinates. These deviations may be caused by inadequate lineal extrapolations. The above mentioned is the routine method used for [q] determination. The procedure is laborious and consumes a considerable amount of time and reactive because of this, several equations were developed which estimate intrinsic viscosity at one single concentration and do not require a graphic. They are known as "single-point" methods. [Pg.91]

Isolating isoprene as the only reactant whose concentration changes simplifies the general rate law to a form that can be tested against the single concentration rate laws ... [Pg.1076]

Because the templates compete for amplification and, in the case of reverse transcription PCR (RT-PCR), also for reverse transcription, any variable affecting amplification has the same effect on both. Thus, the ratio of PCR products reflects the ratio of the initial amounts of the two templates as demonstrated by the function C/W=C (l+ )"/Wi(l+ )n, where Cand Ware the amounts of competitor and wild-type product, respectively, and C and W are the initial amounts of competitor and wild-type template, respectively, (Clementi etal., 1993). From this linear relationship, it could be concluded that a single concentration of competitor could be sufficient for quantitating unknown amounts of wild-type templates. However, in practice, the precise analysis of two template species in very different amounts has proved difficult and cPCRs using three to four competitor concentrations within the expected range of wild-type template concentrations are usually performed. In a recent study of different standardization concepts in quantitative RT-PCR assays, coamplification on a single concentration of a competitor with wild-type template was comparable to using multiple competitor concentrations and was much easier to perform (Haberhausen et al, 1998). [Pg.214]

The charge density on the electrode a(m) is mostly found from Eq. (4.2.24) or (4.2.26) or measured directly (see Section 4.4). The differential capacity of the compact layer Cc can be calculated from Eq. (4.3.1) for known values of C and Cd. It follows from experiments that the quantity Cc for surface inactive electrolytes is a function of the potential applied to the electrode, but is not a function of the concentration of the electrolyte. Thus, if the value of Cc is known for a single concentration, it can be used to calculate the total differential capacity C at an arbitrary concentration of the surface-inactive electrolyte and the calculated values can be compared with experiment. This comparison is a test of the validity of the diffuse layer theory. Figure 4.5 provides examples of theoretical and experimental capacity curves for the non-adsorbing electrolyte NaF. Even at a concentration of 0.916 mol dm-3, the Cd value is not sufficient to permit us to set C Cc. [Pg.227]

The graph in Figure 10.11 shows well how a micelle would forms at a single concentration, rather than over a range. Although a single concentration is a theoretical construct, the concentration range can be remarkably narrow. [Pg.516]

Examples of some typical SDOF approximations were briefly introduced in Section 6.4.1 and illustrated in Figure 6.2. These SDOF models greatly simplify the dynamic analysis effort compared to that of structures having distributed mass, For structures having a single concentrated mass, the SDOF system can be defined without an approximation. [Pg.176]

Intermediate-duration inhalation studies were all single concentration studies at concentrations that resulted in serious effects (26-52 ppm) (Deichmann et al. 1944), or no effects (5 ppm) (Sandage 1961). Therefore, an intermediate-duration inhalation MRL was not derived for phenol. The serious effects noted included pneumonia, necrosis of the myocardium, fatty degeneration of the liver, glomerular degeneration, and hindlimb paralysis (Deichmann et al. 1944). Additional inhalation studies that... [Pg.145]

In contrast to traditional methods for total petroleum hydrocarbons that report a single concentration number for complex mixtures, the fractionation methods report separate concentrations for discrete aliphatic and aromatic fractions. The petroleum fraction methods available are GC-based and are thus sensitive to a broad range of hydrocarbons. Identification and quantification of aliphatic and aromatic fractions allows one to identify petroleum products and evaluate the extent of product weathering. These fraction data also can be used in risk assessment. [Pg.205]

A check of robustness includes preliminary experiments on precision. During robustness testing, a single standard is repetitively analyzed before starting the actual calibration. Without sufficient precision at a single concentration, it is fruitless to calibrate. However, the RSD obtained from repeated injections underestimates the overall error by a factor of up to 3. ... [Pg.235]

In addition to that a quick system-suitability check should be done every day and when a system is restarted. The system-suitability test particularly emphasizes on resolution and sensitivity (single/concentration) or the DL. To save time, the system suitability test should restrict to repeatability of migration time and PA, and to resolution of relevant peak pairs. [Pg.241]

As mentioned above, the ISE potential depends directly on the test ion activity and only indirectly on its concentration. At a single concentration, the individual ion activities can vary considerably in their dependence on the solution composition. [Pg.78]


See other pages where Single concentrations is mentioned: [Pg.259]    [Pg.108]    [Pg.567]    [Pg.104]    [Pg.156]    [Pg.158]    [Pg.159]    [Pg.199]    [Pg.238]    [Pg.255]    [Pg.154]    [Pg.338]    [Pg.72]    [Pg.35]    [Pg.882]    [Pg.95]    [Pg.221]    [Pg.627]    [Pg.15]    [Pg.111]    [Pg.57]    [Pg.311]    [Pg.196]    [Pg.851]    [Pg.213]    [Pg.119]    [Pg.92]    [Pg.110]    [Pg.111]    [Pg.127]    [Pg.203]   
See also in sourсe #XX -- [ Pg.240 ]




SEARCH



Concentration single molecule experiments

Concentration single-file system

Peak plasma concentration single extravascular dose

Reactor concentration single irreversible reactions

Reactor concentration single reversible reactions

Single concentrates

Single concentrates

Single concentration gradients

Single concentration profiles

Single-cell protein, concentrates

Single-chain diffusion concentration dependence

Single-concentration counterscreen

© 2024 chempedia.info