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The Residual Mode

Expression (2.8) will in general not constitute the entire RCS of an antenna. In fact, it is only a component of the total radar cross section, which implies that there may be something else. This is usually called the residual (or structural) component a res- It was defined earlier as whatever must be added to the field associated with a am as given by (2.8) in order to obtain the field associated with the total antenna RCS, that is. [Pg.20]

Inspection of (2.10) might seem to imply thatOre is proportional to GjGrPiPr-This is not necessarily the case. In general it is a more intricate function. In fact, the only reason we write it on the form in (2.10) is that it enables us to add [Pg.20]

More specifically, consider Fig. 2.6, top. We show here a Smith chart normalized to Ra. Recall farther that one of the nnique features of the Smith chart is that the reflection coefficient F as given by (2.2) is a phasor measured from the center Ra of the Smith chart to the modified load impedance Rp + jiXi + Xa) s shown in the Smith chart. The magnitude of the field associated with the antenna mode component is proportional to r [see (2.8)], while the magnitnde of the field associated with the residual mode component is proportional to C [see (2.10)]. Thus, according to (2.9) the field associated with atot is proportional to the magnitude of the phasor sum (T + C) as also shown in the same Smith chart. [Pg.21]

The beauty of this representation is that it clearly shows how Otot varies with the load impedance Zp (as mentioned above, C does not depend on Zp). For example, we may let Zp vary in such a way that the VSWR is constant. In [Pg.21]

We considered above the case where the residual component C was bigger than F. We found that atm could never become zero no matter how we chose our load impedance Z. However, if we instead considered an antenna where C 1 as shown in Fig. 2.6, bottom (there are no particular limitations on C), we readily observe that we can choose the load impedance Zi such that C + F =0 that is, atm min = 0. This technique is referred to as RCS control by cancellation. [Pg.22]


To this end, an additional orthogonal coordinate transformation is introduced, by which the bilinear couplings occurring in Eq. (13) are transformed to a band-diagonal form that only allows a coupling to the (three) nearest neighbors. By concatenating the effective-mode construction described in the previous section with this additional transformation in the residual-mode subspace,... [Pg.196]

Bands can often be assigned by studying their frequency behavior when an isotopic substitution is made in the molecule. An obvious case is the effect of N-deuteration, which, for example, results in the replacement of an NH stretch mode near 3300 cm" by an ND stretch mode in the 2500-2400-cm" region or in the disappearance of amide II, III, and V modes (the first two of which involve major contributions from NH ib and the third of which involves NH ob) and the appearance of ND modes at lower frequencies. For modes with minor contributions from NH deformation, normal-mode calculations are a very important guide in assigning bands Calculations for the N-deuterated molecule indicate explicitly the behavior of the residual mode when the NH contribution is removed, as well as how the ND contribution may mix with other modes in its spectral region, both aspects of which may be specific to the particular structure. [Pg.227]

The residual mode component representing whatever must be added to the antenna mode component to obtain the total RCS. It may or may not depend on the gain G, the polarization, the freqnency, and the angle of incidence, but never on the load impedance Zi. [Pg.17]

The definition of the residual mode admittedly violates a fundamental scientific principle Never explain something unknown by something else unknown. Nevertheless, the concept is extremely useful for understanding antenna scattering. [Pg.17]

It is not unusual to hear the notion that low RCS antennas are obtained by a more or less systematic approach based entirely on computation. This is of course possible. In fact, we addressed this problem in Section 2.3 where we pointed out that any antenna with a residual component C < 1 could indeed produce a low RCS by simply adjusting the load impedance Zl in such a way that cancellation between the antenna mode and the residual mode would occur. As also pointed ont, this condition is not compatible with maximum power transfer, and perhaps worst of all it is usually narrowbanded, sensitive to the angle of incidence and polarization. Thus, these types of solutions are primarily of academic interest and shonld not be propagated as anything else when teaching antenna scattering theory on a practical level. [Pg.48]

We opened this chapter with a review of the classical theory of antenna scattering. The total RCS of any antenna could be written as the phasor addition of two components, namely the antenna and the residual mode components. The first of these was clearly and precisely defined by the antenna gain G, the reflection... [Pg.49]

Fig. 15.1 Schematic illustration of the coupling patterns within the residual-mode subspace, as described in Sect. 15.2.3. The number of effective modes is N ff = 3 in the present example. L Star type pattern, with a diagonal form of the djj matrix in the residual Ng —iVeff)-dimensional subspace middle chain type configuration with a band-diagonal form right truncated chain pattern which re-introduces the star pattern at a higher order of the chain... Fig. 15.1 Schematic illustration of the coupling patterns within the residual-mode subspace, as described in Sect. 15.2.3. The number of effective modes is N ff = 3 in the present example. L Star type pattern, with a diagonal form of the djj matrix in the residual Ng —iVeff)-dimensional subspace middle chain type configuration with a band-diagonal form right truncated chain pattern which re-introduces the star pattern at a higher order of the chain...
In the 2003 NEHRP Recommended Provisions (BSSC 2004) for buildings with passive dampers, and for the equivalent lateral force (ELF) analysis (linear static analysis) specifically, the response is defined by two modes the fundamental mode and the residual mode, which is used to approximate the combined effects of higher modes. For response spectrum analysis, higher modes are... [Pg.401]

The LIN method ( Langevin/Implicit/Normal-Modes ) combines frequent solutions of the linearized equations of motions with anharmonic corrections implemented by implicit integration at a large timestep. Namely, we express the collective position vector of the system as X t) = Xh t) + Z t). (In LN, Z t) is zero). The first part of LIN solves the linearized Langevin equation for the harmonic reference component of the motion, Xh t)- The second part computes the residual component, Z(t), with a large timestep. [Pg.246]

In the sphtless mode, the vent is turned off and everything injected goes onto the column. After a short period, the vent is opened and any residual solvent is vented. The spHdess mode is found particularly in trace analytical schemes (see Trace and residue analysis). Sphtless sample injection is an art, and it requites practice to ensure reproducible introduction of sample onto the column. This type of injection is usually used for quahtative analysis. [Pg.109]

The A-plane is based on the concepts of the modal technique. From Equation (17-5), there are N principal modes that need to be zero for the perfect balance of a rotor, which runs through Mh critical speed. Thus, A-planes located at the peaks of the principal modes will be enough for cancelling these modes. From the point of view of residual forces and moments at the support bearings, (N + 2)-planes are better than A-planes. [Pg.596]

Figure 10.5 Comparison of the sequence-specific binding to DNA of six different zinc fingers. Residues in the N-terminus of the a helix in the finger regions are numbered 1 to 6. The residue immediately preceding the a helix is numbered -1. Amino acid residues and nucleotides that make sequence-specific contacts are colored. In spite of the structural similarities between the zinc fingers and their overall mode of binding, there is no simple rule that governs which bases the fingers contact. Figure 10.5 Comparison of the sequence-specific binding to DNA of six different zinc fingers. Residues in the N-terminus of the a helix in the finger regions are numbered 1 to 6. The residue immediately preceding the a helix is numbered -1. Amino acid residues and nucleotides that make sequence-specific contacts are colored. In spite of the structural similarities between the zinc fingers and their overall mode of binding, there is no simple rule that governs which bases the fingers contact.
When the eore s flux is eompletely emptied prior to the next cyele, it is referred to as the discontinuous-mode of operation. This is seen in the induetor eurrent and voltage waveforms in Figure 3-4. When the eore does not eompletely empty itself, a residual amount of energy remains in the eore. This is ealled the continuous mode of operation and ean be seen in Figure 3-5. The majority of boost-mode eonverters operate in the diseontinuous mode sinee there are some intrinsie instability problems when operating in the eontinuous mode. [Pg.25]

Fig. 4.18. Detection limit ofTXRF for the residues of aqueous solutions, depending on the atomic number of the analyte element. Three excitations modes were used (a) W-tube, 50 kV Ni-fil-ter, cutoff 35 keV (b) Mo-tube 50 kV Mo filter, cutoff 20 keV (c) W-tube,... Fig. 4.18. Detection limit ofTXRF for the residues of aqueous solutions, depending on the atomic number of the analyte element. Three excitations modes were used (a) W-tube, 50 kV Ni-fil-ter, cutoff 35 keV (b) Mo-tube 50 kV Mo filter, cutoff 20 keV (c) W-tube,...
To maintain a high polymerization rate at high conversions, reduce the residual amount of the monomer, and eliminate the adverse process of polyacrylamide structurization, polymerization is carried out in the adiabatic mode. An increase in temperature in the reaction mixture due to the heat evolved in the process of polymerization is conductive to a reduction of the system viscosity even though the polymer concentration in it rises. In this case, the increase in flexibility and mobility of macromolecules shifts the start of the oncoming gel effect into the range of deep transformation or eliminates it completely. [Pg.66]

It is found, however, that in sensitive situations this mode of conditioning may still lead to undesirably high amounts of acidicity or alkalinity. This is caused by the precipitation from solutions of tri-sodium phosphate of material with an excess of sodium so that the residual solute is... [Pg.848]

The characteristic mode of corrosion of some alloys may be the formation as a corrosion product of a redeposited layer of one of the alloy constituents, as in the case of the brasses that dezincify, or of a residue of one of the components, as in the case of the graphitic corrosion of cast iron. Particularly in the case of the dezincified brass, the adherent copper is not likely to be removed with the other corrosion products, and therefore the mass-loss determination will not disclose the total amount of brass that has been corroded. This is especially important because the copper layer has very little strength and ductility and the extent of weakening of the alloy will not be indicated by the mass loss. In these cases, also, the mass-loss determinations must be supplemented by, or replaced by, mechanical tests or metallographic examination, or both, to reveal the true extent of damage by corrosion. Difficulties in obtaining accurate mass losses of heavily graphitised specimens have been reported... [Pg.989]

Therefore, in order to obtain a 1,4-addition of an allyl residue to an enone, two activation modes can be used reactions take place either under electrophilic conditions with Lewis acid promotion, or in the presence of fluoride ions. This is important as the stereochemical outcome often depends on the activation mode selected. [Pg.937]

Some limitations of optical microscopy were apparent in applying [247—249] the technique to supplement kinetic investigations of the low temperature decomposition of ammonium perchlorate (AP), a particularly extensively studied solid phase rate process [59]. The porous residue is opaque. Scanning electron microscopy showed that decomposition was initiated at active sites scattered across surfaces and reaction resulted in the formation of square holes on m-faces and rhombic holes on c-faces. These sites of nucleation were identified [211] as points of intersection of line dislocations with an external boundary face and the kinetic implications of the observed mode of nucleation and growth have been discussed [211]. [Pg.26]


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