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Matching coefficient

Alloys suitable for castings that ate to be bonded to porcelain must have expansion coefficients matching those of porcelain as well as soHdus temperatures above that at which the ceramic is fired. These ate composed of gold and palladium and small quantities of other constituents silver, calcium, iron, indium, tin, iridium, rhenium, and rhodium. The readily oxidi2able components increase the bond strength with the porcelain by chemical interaction of the oxidi2ed species with the oxide system of the enamel (see Dental materials). [Pg.384]

Figure 6.2 Simulated superimposed melting endotherms (dark line). Final simplex-program coefficients match those used for the simulation. Dotted lines are plots of each term in the sum in eq. 6.3, representing the deconvo-luted melting endotherms. Figure 6.2 Simulated superimposed melting endotherms (dark line). Final simplex-program coefficients match those used for the simulation. Dotted lines are plots of each term in the sum in eq. 6.3, representing the deconvo-luted melting endotherms.
For mitochondria, L33 is an overall phenomenological coefficient lumping together all the conductances of ATP-utilizing processes, while Lx x shows the conductance of phosphorylation. If these two coefficients match according to Eq. (11.111), then the natural steady state of oxidative phosphorylation is at the optimal efficiency. Stucki called Eq. (11.111) the condition of conductance matching of oxidative phosphorylation, and presented an experimental verification. [Pg.571]

If the coefficients are calculated for 1-methoxy-1,3-butadiene the termini are -1-0.3 and —0.58 (or —0.3 and -1-0.58). For acrylonitrile the coefficients are -1-0.2 and —0.66 (or —0.2 and -1-0.66). The cycloaddition reaction proceeds so that the coefficients match, in terms of both phase (essential) and coefficient magnitude -1-0.3 with -1-0.2 and —0.58 with —0.66. Thus, the preferred orientation of reactants (diene and dienophile) for the initial bonding interaction is displayed and this orientation agrees with the regioselectivity reported in Fig. 8.33. [Pg.338]

Low thermal expansion coefficient matching that of the co-fired ceramic capsule. [Pg.290]

Figure 3 shows the correlation function and the corresponding spectrum of relaxation times for a solution of sodium poly(styrenesulfonate) (NaPSS) in 3.7 M NaCl. Two modes can be clearly recognized. The slower mode corresponds to the diffusion of polyions, which will be discussed in the next section. The faster mode corresponds to the diffusion of salt (NaCl). As expected for a diffusive process, the inverse relaxation time of this mode Tvf (the subscript vf refers to very fast ) is q2 dependent (Figure 4). The diffusion coefficient of the salt small ions was calculated from the slope of the dependence Tvf = Dwfq2 in Figure 4 as Dvf = (1.7 0.1) X 10 5 cm2s The scattering amplitude of the very fast mode varies proportionally with the salt concentration and is q independent as expected. Figure 5 shows the correlation function and the corresponding spectrum of relaxation times for a pure solution of NaCl in water (no polymer added). Only one diffusive mode is present with the diffusion coefficient matching relatively closely the value of Dvf obtained in polyelectrolyte solution. Figure 3 shows the correlation function and the corresponding spectrum of relaxation times for a solution of sodium poly(styrenesulfonate) (NaPSS) in 3.7 M NaCl. Two modes can be clearly recognized. The slower mode corresponds to the diffusion of polyions, which will be discussed in the next section. The faster mode corresponds to the diffusion of salt (NaCl). As expected for a diffusive process, the inverse relaxation time of this mode Tvf (the subscript vf refers to very fast ) is q2 dependent (Figure 4). The diffusion coefficient of the salt small ions was calculated from the slope of the dependence Tvf = Dwfq2 in Figure 4 as Dvf = (1.7 0.1) X 10 5 cm2s The scattering amplitude of the very fast mode varies proportionally with the salt concentration and is q independent as expected. Figure 5 shows the correlation function and the corresponding spectrum of relaxation times for a pure solution of NaCl in water (no polymer added). Only one diffusive mode is present with the diffusion coefficient matching relatively closely the value of Dvf obtained in polyelectrolyte solution.
The above analysis, however, is not applicable to phthalic anhydride 127. The electron-donating and electron-withdrawing substituents should make the reaction selective for attack at Cp and Ca, respectively, due to the relatively larger LUMO coefficients on these positions. Except for R = Me, when the values are hardly different, the LUMO coefficients match this expectation. However, in spite of being sterically disfavored, the attack by NaBH4 takes place preferably at Ca of all the three substrates Ca Cp = 87 13 for R = OMe, 57 43 for R = Me, and 83 17 for R = NO2. Thus, the overall situation remains unclear and no suitable rationale could be offered to explain the observed selectivity. [Pg.179]

Category III noise Is reduced by strategies combining optimization of both detector and non-detector hardware as In reduction of reciprocating pump pulsation, the use of low thermal coefficient, matched pairs of photodiodes for reference and sample beam optical trains, and thermal coupling of reference and sample photodiodes. Pump pulsation noise can also be reduced by proper flow cell design ( ). [Pg.109]

After IC devices are manufactured on a substrate wafer, a dicing saw is used to break the wafers into smaller chips. The chips are then bonded to a metal frame (called a lead frame) using epoxy. The lead frame is often made of Cu-Ni-Fe alloys with a thermal expansion coefficient matched with that of the silicon substrate as well as of the plastic compound. Wire bonding is used to connect contact pads on the device to the lead frame. The device (and the lead frame) is then put into a mold. The plastic compound, with a thermal expansion coefficient matched with silicon, is molded around the deviceAead frame to form a protective case. [Pg.2644]

MS-SOFCs are not only cost efficient, but they also promise other advantages such as robusmess and tolerance to rapid thermal- and redox-cycling. Ferritic stainless steel is a widespread candidate for the support, because it is cheap, its thermal expansion coefficient matches closely with that of metal interconnects and it has a good high temperature oxidation resistance... [Pg.77]

Shao and Haile (2004) suggested a material based on strontium-doped barium cobaltite ferrite [BaFe03 Bai xSrjcCoyFei 3,03 (BSCF) (0.1 data reported by Wei et al. (2005), difficulties arise because of the complex temperature dependence of the thermal expansion coefficient. According to results obtained by Lim et al. (2(K)7), this coefficient matches that of the electrolyte when x = 0.2. [Pg.151]


See other pages where Matching coefficient is mentioned: [Pg.363]    [Pg.504]    [Pg.79]    [Pg.538]    [Pg.643]    [Pg.338]    [Pg.347]    [Pg.419]    [Pg.518]    [Pg.3]    [Pg.2644]    [Pg.748]    [Pg.206]    [Pg.1594]    [Pg.1594]    [Pg.186]    [Pg.80]    [Pg.83]    [Pg.158]    [Pg.10]    [Pg.26]    [Pg.31]   
See also in sourсe #XX -- [ Pg.304 ]




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