Big Chemical Encyclopedia

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

Articles Figures Tables About

X -value

CONOUCT NEWTON-RAPHSON ITERATION FOR A AT FIXED X VALUES... [Pg.337]

The older t scale places TMS at IOt with most protons bonded to carbon having smaller X values. [Pg.391]

The deviation of Gibbs monolayers from the ideal two-dimensional gas law may be treated by plotting xA// 7 versus x, as shown in Fig. III-15c. Here, for a series of straight-chain alcohols, one finds deviations from ideality increasing with increasing film pressure at low x values, however, the limiting value of unity for irAfRT is approached. [Pg.83]

This form is obeyed fairly well above x values of 5-10 dyn/cm in Fig. Ill-15c. Limiting areas or a values of about 22 per molecule result, nearly independent of chain length, as would be expected if the molecules assume a final orientation that is perpendicular to the surface. Larger A values are found for longer-chain surfactants, such as sodium dodecyl sulfate, and this has been attributed to the hydrocarbon tails having a variety of conformations [127]. [Pg.83]

The maximum number of latent variables is the smaller of the number of x values or the number of molecules. However, there is an optimum number of latent variables in the model beyond which the predictive ability of the model does not increase. A number of methods have been proposed to decide how many latent variables to use. One approach is to use a cross-validation method, which involves adding successive latent variables. Both leave-one-out and the group-based methods can be applied. As the number of latent variables increases, the cross-validated will first increase and then either reach a plateau or even decrease. Another parameter that can be used to choose the appropriate number of latent variables is the standard deviation of the error of the predictions, SpREss ... [Pg.725]

The ability of partial least squares to cope with data sets containing very many x values is considered by its proponents to make it particularly suited to modern-day problems, where it is very easy to compute an extremely large number of descriptors for each compound (as in CoMFA). This contrasts with the traditional situation in QSAR, where it could be time-consuming to measure the required properties or where the analysis was restricted to traditional substituent constants. [Pg.727]

X in subsequently solving for the v veetor s eoeffieients. That is, eaeh X value has its own veetor V. [Pg.527]

One ean substitute eaeh of these n X values ()ik, k = l,2,n) baek into the eigenvalue... [Pg.527]

Since we have ended up with a continuous distribution function, it is more appropriate to multiply both sides of Eq. (1.34) by dx and to say that the equation gives the probability of x values between x and x + dx for n steps of length 1. [Pg.47]

Very early in the study of radioactivity it was deterrnined that different isotopes had different X values. Because the laws of gravity and electromagnetism were deterministic, an initial concept was that when each radioactive atom was created, its lifetime was deterrnined, but that different atoms were created having different lifetimes. Furthermore, these different lifetimes were created such that a collection of nuclei decayed in the observed manner. Later, as the probabiUstic properties of quantum mechanics came to be accepted, it was recognised that each nucleus of a given radioactive species had the same probabiUty for decay per unit time and that the randomness of the decays led to the observed decay pattern. [Pg.446]

The product is equal to the equilibrium constant X for the reaction shown in equation 30. It is generally considered that a salt is soluble if > 1. Thus sequestration or solubilization of moderate amounts of metal ion usually becomes practical as X. approaches or exceeds one. For smaller values of X the cost of the requited amount of chelating agent may be prohibitive. However, the dilution effect may allow economical sequestration, or solubilization of small amounts of deposits, at X values considerably less than one. In practical appHcations, calculations based on concentration equihbrium constants can be used as a guide for experimental studies that are usually necessary to determine the actual behavior of particular systems. [Pg.391]

The X values for some common scale deposits and nittilotriacetic acid (NTA), which is an effective agent for solubilizing CaSO and CaSiO ... [Pg.391]

The isomeric 2-phenyla2o-l-naphthols (12) [1602-36 ] and l-phenyla2o-2-naphthols (13) [1602-30-8] exist more ia the hydra2one form than the a2o form as shown bv thek uv spectra. Then X values are each about 500 nm. [Pg.275]

Once the form of the correlation is selected, the values of the constants in the equation must be determined so that the differences between calculated and observed values are within the range of assumed experimental error for the original data. However, when there is some scatter in a plot of the data, the best line that can be drawn representing the data must be determined. If it is assumed that all experimental errors (s) are in thejy values and the X values are known exacdy, the least-squares technique may be appHed. In this method the constants of the best line are those that minimise the sum of the squares of the residuals, ie, the difference, a, between the observed values,jy, and the calculated values, Y. In general, this sum of the squares of the residuals, R, is represented by... [Pg.244]

If the units of production may not he subdivided, the procedure is similar except that all X values are increased by 0.5 unit in establishing the curves. The results are not sufficiently different to he significant for estimation purposes. [Pg.821]

When X represents a continuous variable quantity, it is sometimes convenient to take the total or relative frequency of occurrences within a given range of x values. These frequencies can then be plotted against the midvalues of x to form a histogram. In this case, the ordinate should be the frequency per unit of width x. This makes the area under any bar proportional to the probability that the value of x will he in the given range. If the relative frequency is plotted as ordinate, the sum of the areas under the bars is unity. [Pg.821]

Repetition of the calculations with N = 7.0 gives R = 2.519, R = 0.9782, and a calculated check value of N = 6.85, which is close enough. The final-product compositions and the (X values used are as follows ... [Pg.1275]

VALUE OF THE INDEPENDENT AND DEPENDENT VARIABLES X-VALUES Y-VALUE S ... [Pg.92]

The eomputer program PROG52 ean be used to solve any number of nonlinear equations. The partial derivatives of the funetions are estimated by the differenee quotients when a variable is perturbed by an amount equal to a small value (A) used in the program to perturb the X-values. [Pg.334]

With high temperatures the x values will not fit into the diagram. Then the hj values have to be calculated with smaller x values in order to draw the isotherms. In Table 4.6 these values are calculated with values x = x q% at various temperatures. Drawing the fundamental axes and isotherms with the instructions given above and the saturation curve with the help of Table 4.6 leads to the Mollier diagram in Fig 4,10u. [Pg.75]

Noting J m = 95g enables the x, values to be calculated from equation 1.32 and the (j) value from equation 1.33. [Pg.23]

X is an acidity function based on the first-order approximation, Eq. (8-92). Values of X have been assigned by an iterative procedure. The data consist of values of Cb/cbh+ as functions of Ch+ for a large number of indicators. For each indicator an initial estimate of pXbh+ and m is made and X is calculated with Eq. (8-94). This yields a large body of X values, which are fitted to a polynomial in acid concentration. From this fitted curve smoothed X values are obtained, and Eq. (8-94), a linear function in X. allows refined values of pXbh + and m to be obtained. This procedure continues until the parameters undergo no further change. Table 8-20 gives X values for sulfuric and perchloric acid solutions. ... [Pg.451]

The hydrogen effect on ductility and the flow stress will be considered first on the example of non-alloyed titanium. The Ti - H phase diagram is given in Fig. 1, and Fig. 2 shows the temperature dependence of ductility of Ti-a H alloys, A , for several X values. Tensile tests were run at a rate e 10" s . Ductility of the commercial... [Pg.427]

For assumed X values, calculate Y corresponding for key component from... [Pg.111]


See other pages where X -value is mentioned: [Pg.33]    [Pg.83]    [Pg.66]    [Pg.85]    [Pg.329]    [Pg.722]    [Pg.329]    [Pg.43]    [Pg.171]    [Pg.432]    [Pg.349]    [Pg.360]    [Pg.487]    [Pg.491]    [Pg.744]    [Pg.821]    [Pg.1684]    [Pg.93]    [Pg.235]    [Pg.398]    [Pg.36]    [Pg.1017]    [Pg.23]    [Pg.220]    [Pg.67]    [Pg.89]   


SEARCH



Another Way to Plot Two Different Sets of X and Y Values

Hat Matrix (x Values)

Plotting Two Different Sets of X and Y Values in the Same Chart

Plotting two different sets of x and y value

Value of X,mm and

X G value

© 2024 chempedia.info