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*B:PE1# configure router ldp *B:PE1>config>router>ldp$ interface-parameters *B:PE1>config>router>ldp>if-params$ interface toPE2 *B:PE1>config>router>ldp>if-params>if$ exit *B:PE1>config>router>ldp>if-params# exit *B:PE1>config>router>ldp# no shutdown *B:PE1>config>router>ldp#

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The dissolved electrolyte must have the following properties: (a) The electrolyte in the aqueous phase, BXAX (assumed to dissociate completely to form cation B ^ and anion A ^ ) , is strongly hydrophilic, while the electrolyte in the organic phase, B2A2 (completely dissociated to cation B 2 + and anion A2~), is strongly hydrophobic These properties can be expressed quantitatively by the conditions for the distribution coefficients between water and the organic phase k^ Ax and k^ Al: <oAl l, ^ A 2 1 (b) The equilibria of the exchange reactions Bi+(w) + B2+(o) ^ Bj+(o) + B2+(w) Ar(w) + A 2 -(o) Ar(o) + A2~(w) (4516).

2. Once both routers have LDP configured, verify that LDP is correctly configured on both PE routers and that they have established an LDP session.

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241 are shifted to the left In other words, the standard potential difference between water and the organic phase for the transfer of the cation of the aqueous phase and the anion of the organic phase must be as positive as possible and the corresponding potential difference for the cation of the organic phase and the anion of the aqueous phase must be as negative as possible In addition, there must be a sufficiently large difference between the less positive value of A 0 for the first pair and the less negative value for the second pair (cf Section 328) Under these conditions, the potential difference between the two phases AQ0 can be changed by charge injection from an external electric current source The appropriate experimental arrangement is shown in Fig 518 E J W Verwey and K F.

*B:PE1>config>router>ldp# show router ldp interface ============================================================ LDP Interfaces ============================================================ Interface Adm Opr Hello Hold KA KA Transport Factor Time Factor Timeout Address -----------------------------------------------------------toPE2 Up Up 3 15 3 30 System -----------------------------------------------------------No. of Interfaces: 1 ============================================================ *B:PE1>config>router>ldp# *B:PE1>config>router>ldp# show router ldp session ==================================================================== LDP Sessions ==================================================================== Peer LDP Id Adj Type State Msg Sent Msg Recv Up Time -------------------------------------------------------------------150.10.0.1:0 Link Established 60 61 0d 00:02:36 -------------------------------------------------------------------No. of Sessions: 1 ==================================================================== *B:PE1>config>router>ldp# exit *B:PE1#

Niessen described the electric double layer at ITIES using a simplifying assumption that consists of only two diffuse electric layers, each in one of the phases (see Fig 41C) The overall potential difference between the two phases, A^^, is thus given by the relationship A:0 = 0 2 (o)-0 2 (w) (4518) where the potential differences in the diffuse layers, 02(o) and 02(w), are defined such that the potential in the bulk of the phase is subtracted from the potential at the interface The terms <j)2{o) and $2(w) are given by Eq (4314), where the appropriate permittivity, e(w) or e(o), is substituted for each phase, along with the electrolyte concentrations c(w) and c(o) As the surface charges a(w) and a(o) are equal except for the sign (cf Eq 411), Eqs (4518) and (43.