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The Playback menu is only accessible when the G11 is in Playback mode. Some of the menu items are used to set parameters for image playback and others actually perform camera functions.



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219 decreasing to as little as 6 at potentials more distant from Epzc (for the mercury-water interface; these values vary with the electrode metal) It can be seen from Fig 45 that a maximum (or 'hump') appears at potentials somewhat more positive than the potential of the electrocapillary maximum on the differential capacity-potential curve This capacity maximum can be explained by postulating that, in the corresponding potential range, the orientation of the water molecules is minimal, ie the permittivity is maximal; at more positive potentials, the water dipoles are oriented so that their negative ends (ie the oxygen atoms) are directed towards the electrode surface while at more negative potentials this orientation is reversed The disagreement between the potential of the 'hump' and the potential of the electrocapillary maximum is apparently a result of weak chemical interaction between the water molecules and the surface of the electrode.





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3. Confirm that a debug log is still configured using the show log log-collector command (from Lab 2.2 in 2). All logs except 99 and 100 disappear every time you log out. If necessary, re-create the log (see Lab 6.1 in 6). Do the same for router PE2. 4. Turn on debugging for ICMP only (see Lab 6.1 in 6). Do the same for router PE2. 5. Test the new static route by pinging the system interface of PE2 from PE1.

It should be noted that the dependence of the differential capacity for some mercury-solvent interfaces is simpler than that for water (eg for methanol or formic acid) and for others is more complicated (propylene carbonate, dimethylsulphoxide, sulpholane, etc) In water, the hump disappears at higher temperatures The picture of the compact double layer is further complicated by the fact that the assumption that the electrons in the metal are present in a constant concentration which discontinuously decreases to zero at the interface in the direction towards the solution is too gross a simplification.

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*B:PE1# ping 150.10.0.1 PING 150.10.0.1 56 data bytes 1 2000/01/01 13:49:07.77 UTC MINOR: DEBUG #2001 Base PIP PIP: ICMP instance 1 (Base), interface index 3 (toPE2), ICMP egressing on toPE2: 140.10.0.1 -> 150.10.0.1 type: Echo (8) code: No Code (0) [... Additional output omitted ...]

Indeed, Kornyshev, Schmickler, and Vorotyntsev have pointed out that it is necessary to assume that the electron distribution in the metal and its surroundings can be represented by what is called a 'jellium': the positive metal ions represent a fixed layer of positive charges, while the electron plasma spills over the interface into the compact layer, giving rise to a surface dipole This surface dipole, together with the dipoles of the solvent molecules, produces the total capacity value of the compact double layer Specific adsorption occurs, ie ions enter the compact layer, in a considerable majority of cases The most obvious result of specific adsorption is a decrease and shift in the maximum of the electrocapillary curve to negative values because of adsorption of anions (see Fig 42) and to positive values for the adsorption of cations.

Request timed out. icmp_seq=1. Request timed out. icmp_seq=2. [... Additional output omitted ...]

The Slideshow menu presents three options for controlling the way your slide show plays back. Use the 4-Way Controller s area buttons to navigate these settings. Repeat. Sometimes called loop, with this control you can set the G11 to replay the slide show once the camera has shown all the images, or you can set it to stop with the last photo. Play Time. This setting determines how long each image is displayed. Choose from 3, 4, 5, 6, 7, 8, 9, 10, 15, or 30 seconds.

A layer of ions is formed at the interface only when specific adsorption occurs By means of the thermodynamic theory of the double layer and the theory of the diffuse layer it is possible to determine the charge density ox corresponding to the adsorbed ions, ie ions in the inner Helmholtz plane, and the potential of the outer Helmholtz plane 0 2 in the presence of specific adsorption The charge density of specifically adsorbed ions (assuming that anions are adsorbed specifically while cations are present only in the diffuse layer) for a valence-symmetrical electrolyte (z+ = z_ = z) is ax = -zF(TA - r A -, d ) = - z / T A - f l (4315).

[ Output captured from PE2 terminal session ] *A:PE2# 1 2000/01/01 13:48:12.54 UTC MINOR: DEBUG #2001 Base PIP PIP: ICMP instance 1 (Base), interface index 3 (toPE1), ICMP ingressing on toPE1: 140.10.0.1 -> 150.10.0.1 type: Echo (8) code: No Code (0)

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