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EACF

The ACF shows a decaying cyclic pattern whereas the PACF clearly indicates a significant partial auto-correlation at lag 1. Therefore, an AR(1) model is chosen as the initial model. To incorporate the outlier at index 128, an ARX(l) model is fitted to the original Naphtha time series where a dummy variable xt accounts for the effect of the outlieP  [Pg.42]

The corresponding residuals standard deviation is estimated as a = 0.002 and the model s AIC) is calculated as -8.13. An analysis of the residuals reveals no hints for a violation of the underlying assumption of independent and identically distributed residuals. [Pg.42]

Jarque-Bera s test for normality confirms that the hypothesis of normally distributed residuals cannot be rejected (at a 5% level), i.e. it -is assumed that e A (0, 0.002 ). Due to the already convincing results of the ARX(l) model (which has minimal order) no other ARMA models of higher order are estimated and (2.66) is taken as the best m,odel for the Naphtha time series. [Pg.43]


The second-order rate constant of H with common radical scavengers is relatively small. However, it is large enough to account for the removal of organic compounds. The high-energy electron beam process is the only process that produces these radicals. Table 12.3 summarizes the reaction rate constants of major organic pollutants with OH, eacf, and H. [Pg.479]

In this study the molecular orbital calculation program employed, ARCANA, utilized only atomic data and iterated to charge self-consistency (see Calculation Note). The substrates, ACh and ASCh, and the products of hydrolysis, choline, thiocholine, and acetic acid, were represented in their entirety, while the AChE enzymic active site was modeled by representing the histidine residue and the serine residue thought to be at the active site by imidazol and methanol respectively. Molecular orbital calculations have been performed for reactants, three possible intermediate acylation complexes, and the acylation products. Since the deacylation mechanism is identical for both ACh and ASCh and has been reported elsewhere (14), those results will not be repeated here. For eacF of the acylation steps, three cases were calculated (a) general acid catalyzed,... [Pg.297]

To decide on the order of time series models as well as to check residuals for the white noise assumptions, auto-correlations of time series and residuals need to be calculated and analysed. Standard metrics to analyse for time-dependent correlation structures are the autocorrelation function (ACF), partial ACF (PACF) and extended ACF (EACF). The ACF estimates the empirical auto-correlations between lagged observations... [Pg.36]

Unfortunately, neither PACF nor ACF lead to directly interpretable results for ARMA processes. The extended ACF tries to overcome this drawback by jointly providing information about the order of both components. For each AR order tested, the EACF first determines estimates of the AR coefficients by a sequence of regression models. Afterwards, the residuals ACF is calculated. The results are presented in a table indicating significant or non-significant auto-correlations (typically denoted by an x and o, respectively). In such a table, the rows represent the AR order p whereas columns represent... [Pg.36]

ACF, PACF and EACF are appUed to time series data to initially estimate the type and order of the underlying time series model. Once an initial model is fitted, ACF, PACF and EACF are applied to the corresponding residuals to check the white noise assumptions. If significant auto-correlations are found, the model type or order is adjusted accordingly and the procedure is repeated until the residuals do not show any serious auto-correlations. [Pg.37]

For the small sample, the EACF values (Table 2.3) show an ambiguous pattern. Probably, an ARMA(1,3) or ARMA(3,1) model viould be chosen as initial choices. In contrast, the large sample (Table 2.).) shows a good fit to the theoretical EACF (Table 2.5) and an ARMA(2,1) model seems an appropriate initial choice. Since the analysis of ACF, PACF and EACF cannot reveal an unambiguous favourite model for both samples, all possible order specifications with p 0,4 and q e 0,4 are estimated for both samples. The corresponding AIC , SIC, and HQIC values are displayed in Table 2.6 where the minimum for each criterion and time series is set in bold font and the true model order is coloured in grey. ... [Pg.38]

B. Effects of overexposure to /eacf—(1) Short term (acute) overexposure. Lead is a potent, systemic poison that serves no known useful function once absorbed by your body. Taken in large enough doses, lead can kill you in a matter of days. A condition affecting the brain called acute encephalopathy may arise which develops quickly... [Pg.248]

Figure 49 Two routes to partial shell filled tecto(dendrimers). Route I involves amidation of a limited amount of nucleophilic core dendrimer with an excess of electrophilic shell dendrimer reagent to produce reactive (PS CST)-[Dc-N-X]-a/n/de- Ds-E-Y n. These products may be pacified by reacting with 2-aminoethanol (EA) or fris(hydroxymethyl) aminomethane trie) to produce shell pac///saf-(PS CST)-[Dc-N-X]-a/r7/de- Ds-E-Z n. Route II involves amidation of a limited amount of electrophilic core dendrimer with an excess of nucleophilic shell dendrimer reagent to produce r eacf/Ve-(PS CST)-[Dc-E-Y]-am/cfe- Ds-N-X n. These products may be converted to pacified forms by reacting with 2-aminoethanol (EA) or an excess of EDA to produce core pacified-(PS CST)-[Dc-E-Z]-am/de- Ds-N-X . Figure 49 Two routes to partial shell filled tecto(dendrimers). Route I involves amidation of a limited amount of nucleophilic core dendrimer with an excess of electrophilic shell dendrimer reagent to produce reactive (PS CST)-[Dc-N-X]-a/n/de- Ds-E-Y n. These products may be pacified by reacting with 2-aminoethanol (EA) or fris(hydroxymethyl) aminomethane trie) to produce shell pac///saf-(PS CST)-[Dc-N-X]-a/r7/de- Ds-E-Z n. Route II involves amidation of a limited amount of electrophilic core dendrimer with an excess of nucleophilic shell dendrimer reagent to produce r eacf/Ve-(PS CST)-[Dc-E-Y]-am/cfe- Ds-N-X n. These products may be converted to pacified forms by reacting with 2-aminoethanol (EA) or an excess of EDA to produce core pacified-(PS CST)-[Dc-E-Z]-am/de- Ds-N-X .

See other pages where EACF is mentioned: [Pg.151]    [Pg.218]    [Pg.487]    [Pg.233]    [Pg.836]    [Pg.48]    [Pg.4]    [Pg.843]    [Pg.37]    [Pg.37]    [Pg.38]    [Pg.39]    [Pg.39]    [Pg.261]    [Pg.74]    [Pg.255]    [Pg.246]    [Pg.525]   


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