Investigatins on Broadband Planar Dipole Antennas

This thesis Entitled Investigations on Broadband planar Dipole Antennas. An antenna is a device ordinarily used for both transmitting and receiving electromagnetic energy. It is an integral part of the radio communication system and accounts for a good deal of progress that has been made in this field during the last few decades.The effect of flaring the dipole arms is studied in Section 4.1. It is observed that the flaring modifies the impedance characteristics of the dipole. In particular, the change in the reactive part of the impedance with frequency is controlled considerably. This improves the 2:1 VSWR bandwidth of the antenna. The effect of various other design parameters on the impedance bandwidth of the antenna are also studied. The important conclusion drawn is that, there is considerable improvement in the impedance bandwidth of the dipole when ground arm dimensions are larger than the main arm dimensions. Theoretical analysis of various cavity backed antennas are given in Chapter 6. The experimental values agree well with the computation. Also the theory gives a clear inside view and explains the reasons for bandwidth enhancement due to flaring and end-loading of the dipole arms. The percentage bandwidth is determined by calculating the Q of the antenna. Since the approach is for the analysis of microstrip antenna on thick grounded substrate, this method cannot be used to predict the impedance bandwidth of the antennas without cavity backup. Also, the structures analysed are simplified versions of the optimised ones. Specially, the arms overlapping is neglected in the analysis. Also, the antennas with symmetrical arms can only be analysed with this theory.

FT-IR and FT-Raman study of Nasicon type phosphates, ASnFe(PO4)3 [A=Na2, Ca, Cd]

FT-Raman and FT-IR spectra of ASnFe(PO4)3 [A=Na2, Ca, Cd] were recorded and analyzed. The bands were assigned in terms of the vibrational group frequencies of SnO6 octahedral and PO4 tetrahedral. The spectral analysis shows that the symmetry of corner shared octahedral (SnO6) and the tetrahedral (PO4) are lowered from their free ion symmetry state. The presence of Fe3+ ions disrupts the S–N–O–S–N chain in the structure. This causes distortion of SnO6 and PO4 in the structure of all the compounds. Also it is seen that there are two distinct PO4 tetrahedra of different P–O bond lengths. One of these tetrahedra is linearly distorted in all the title compounds. The PO4 frequencies and bond lengths are calculated theoretically and are in agreement with the experimental values. The presence of PO4 polyanion in the structure can reduce the redox energy and hence reduce the metal oxygen covalency strength in the structure