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Full stepping

There exists a point of view that the main mechanism of electrochemical corrosion is assoceated with a full step by step oxidation of graphite to C02 during the cycling, according with reaction (3), [2],... [Pg.405]

The synthetic plan in Figure 6 has been realized as full steps shown in Figure 7. C-Glycosidation of 18 with phenylthiotrimethylsilyl-acetylene and boron trifluoride etherate followed by treatment with biscobaltoctacarbonyl gave the biscobalthexacarbonyl complex 25 in 92% yield. Epimerization of the cobalt complex 25 was achieved with trifluoromethane sulfonic acid in... [Pg.186]

From the above it may be clear that MD, MC and stochastical methods tend to the half-wav point is then used for taking the full step. [Pg.180]

Local approximations (linear or quadratic) are often particularly poor in dynamic optimization problems. For instance, this situation is found to occur when taking the full step predicted from the local approximation, 6, causes a path constraint to become active or the system to become unstable. [Pg.340]

The patient received his sixth therapy. The patient stated at that time that he felt much better. He ambulated a small amount on the weekend. He was able to walk up one full step, which was considered quite a feat by his family and himself. [Pg.100]

In the application of these relationships, ek is set equal to sk, which amounts to using a full step size to approximate the total derivative see Eq. (15-51). The numerical value of sk is picked such that convergence is promoted that is, for the /cth trial, sk is picked such that the euclidean norm (see App. A) of fk+1 is less than the euclidean norm of fk, that is,... [Pg.578]

Second, in polyketide synthesis, the full steps of p-carbonyl reduction (ketoreduction, dehydration, and enoylreduction) are not always involved after every condensation as in fatty acid synthesis. The keto group in the polyketide backbone results from the lack of ketoreduction after the condensation step. Similarly, the hydroxyl group at the P position results from ketoreduction and failure to undergo the subsequent dehydration step, the a,p unsaturated group results from ketoreduction and dehydration steps, and the methylene group results from the full steps of reduction after the condensation. After all steps of condensation and P-carbonyl reduction are completed, the resulting acyl residue is released from polyketide synthases by thioesterase (TE) and spontaneous lactonization proceeds. [Pg.288]

A full step by step procedure was written which included aUocated time per activity and responsible person. As mentioned earher the Procedure, Critical Path Schedule and Risk Assessment were synchronized and reference points was made to assist with ease of use. [Pg.557]

There are twelve keys on a piano keyboard from A to G, and this represents twelve half steps, or intervals. The distance between two notes can be described in terms of steps. The distance between E and F is one half step (one semitone), while the distance between D and E is one full step (one tone or two semitones). Chords can simply be described in terms of intervals, or the distance between the various notes that make up the chord. For example, a chord called a C major triad could be described as a C root note, a second note four semitones higher, and another note seven semitones above the root. Expressed numerically, a major triad might be described as a 0-4-7 chord. Unfortunately, life is not so simple. [Pg.67]

Obviously, it would be a bit tedious to click through the menus, one semitone at a time, until the desired pitch is achieved. An easier method of changing the pitch of a track quickly is to click on the Track Header to select it and then press the + or - keys on your keyboard s number pad repeatedly. For example, pressing the -I- key twice raises the pitch of the track a full step. [Pg.76]

Section 3-4 presented the mechanism for the chlorination of methane in full, step-by-step detail. Section 3-5 discussed the reactions of methane with the other three halogens, but it did not actually display either the full equations for any of these reactions, nor did it illustrate any of the individual steps of their mechanisms. Why not The reactions of methane with the four halogens all proceed through mechanisms that are qualitatively identical to one another. To write a mechanism for the reaction of methane with fluorine, bromine, or iodine you need only (1) copy the mechanism for reaction with chlorine and (2) replace every Cl in those equations with the symbol for the new halogen. The energy values will be different because the bond strengths are different, but the overall appearance of the mechanisms will be the same. Solved Exercise 3-4 already illustrated this strategy for the chlorination of ethane. Let us try some examples ... [Pg.113]

A simple test for checking the step size is to do the calculations at each interval twice Once with the full step size, and then repeat the calculations over the same interval with a smaller step size, u.sually half that of the first one. If at the end of the interval, the difference between the predicted value of y by both approaches is less than the specified convergence criterion, the step size may be increased. Otherwise, a larger than acceptable difference between the two calculated y values suggests that the step size is large, and it should be shortened in order to achieve an acceptable truncation error. [Pg.352]


See other pages where Full stepping is mentioned: [Pg.345]    [Pg.236]    [Pg.417]    [Pg.426]    [Pg.407]    [Pg.70]    [Pg.397]    [Pg.339]    [Pg.345]    [Pg.397]    [Pg.88]    [Pg.117]    [Pg.89]    [Pg.198]    [Pg.511]    [Pg.438]    [Pg.447]    [Pg.417]    [Pg.647]    [Pg.402]    [Pg.287]    [Pg.79]    [Pg.81]   
See also in sourсe #XX -- [ Pg.13 , Pg.25 ]




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