13L «45» 3&5 "u 381* 9 a. o . xx .. .5 1..“ .. 2. .. o“ .. a . 8 a _ in» 1.9 v.3 3m . . 5.». h ‘0“ 4-. q .4. n .3... ‘5”: m. . . é . x. g... “L '3 o s o u .a 9- .. so ‘ .3 s a. -A .5... ....u w. r...“ .Y.. rb ...\.. «a . a“, l . a .w. . . $6.... X3 - ”U u _ V. ‘33 7 AV "flu. « h . L. :3. . 9‘ . . 4 M Jk n fi.‘ ‘v I 'C“ 0r: - o O '0 an. 4&9 \ . {.0 o 0. ..h “a a“ fix Mia» luw m V): v.‘ .1 a a 4 . .. .3. u r: k 8. Ab , 3. «iv “NJ! «to h c .1“ .5.» ‘ ‘ {to bars. H:_:__:_itSEE::_:__:_E___:_E__ mwm W ‘11mmmijlngmanu LIBRARY Mlchigan State University This is to certify that the thesis entitled A Radio-Frequency Pulse Generator for UltraSOnic Studies presented by Walter G. Meyer has been accepted towards fulfillment of the requirements for 15.8. degreem P sites in /A. ;&1LobAA¢ADHAa Major professor Date July 29: 1955 0-169 ___.____.___._. _ _ ML. _ _ ._ _ ‘_ ___ _. _. _ __, A__ _ __ _. PLACE IN RETURN BOX to remove this checkout from your record. To AVOID FINE return on or before date due. MAY BE RECALLED with earlier due date if requested. DATE DUE DATE DUE DATE DUE we WW“ A RADIO—-FREQUENCY PULSE GENERATOR FOR ULTRASONIC STUDIES By Walter Georg Mayer A THESIS Submitted to the School of Graduate Studies of Michigan State University of Agriculture and Applied Science in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE Department of Physics 1955 ACKNOWLEDGEMENT I should like to thank Dr. E. A. Hiedemann, who suggested the construction of the apparatus, for his guidance throughout the experiments and for his willingness to offer helpful suggestions (MW and advice. A RADIO- FREQUENCY PULSE GENERATOR FOR ULTRASONIC STUDIES BY 'Walter Georg mayer AN ABSTRACT Submitted to the School of Graduate Studies of Michigan State University of Agriculture and Applied Science in partial fulfillment of the requirements for the degree of MASTER.OF SCIENCE Department of Physics 1955 I ch )h- QKLLDLLAA~° °. 39 "" L I a -@ H1 .1 kg ”“ __ ‘ flu Jim ’@ 3 :4 _l g 9 3 3W 3 s: | or LW 4 9 ___I_ l U I 8 - 0~ at “I 1% d c U " 4%" > > ® " 8 —\~ 3 I , 3 " -- ._ . a J °‘ : [7 ID I, 23 o If a l _J *W“ * T” 5 3 0 g! 3r ‘ t + _QDQVOWNV“1 i _ ‘ J or ' 5' O—-*% 3 J—s: I E C an X It“ U o: M TV A ‘ l + r---- '6 ”T b a ___q * O O _. O O 3—,,— d ‘ “N, u U _— ‘5: If on) “O 1 tavern-r <>—-—~ uaeerdi 1x3 ”A4” Fig. 10. Multivibrator 21 39VIKV\H9H1 T I A ~---4 (E C? .LnO'VH )5: _mL .Omz Power Amplifier Fig. 11. 22 «L 01’ >md D w, u} 7 JV 0‘63 493!” 0' 123 3A Q—‘ no U x08 I mm»! <-“I NOILV __l inéNl Receiver Fig. 12. 23 F. List of Components Multivibrator: Resistances (R). 3 680K 4 1.2Meg 5 120K 6 300K var. 7,13 10K 5W 8 25K 10W 9 220K 10 6.8K 11,14,18 39K 12 68K 15 25K 16,17 2.2K 19 81K 20 330K 21,24 400 var. 22 470K 23 5.1K 33,34 450 SW 35 20K 10W 36 8K 5W gower Supplies: Resistances‘TR). 1 43K 200W 2 130K 50W Inductances (L). Capacitors (C). 5 lSmmf 659,10 24mmf 7,12,17,18 .01 8 .001 11 .047 13 .0015 14 920mmf 15 .02 16 300mmf var. 32-33-34 50-40-30 350V 35 250mmf Tubes (V). Inductances (L). 6SN7 5 9 microh 5 6A0? 6 5.5 microh 6 884 7 17 microh 6J5 8 5 microh Capacitors (C). 1,2 4 1000V ele. 3 l6 450V ele. 4 20 450V ele. Transformers (T). RFC l 2.5 mh Tubes (V). 1 5Y3 2,3 866A 1 5/25 hy 1 375-0-375, 5v-3amp. 6.3v-1.8amp 2 20 hy 2 Variac 3 5 hy 3 2150-0-2150 4 l4 hy 4 2.5V-10amp gower Amplifier: Resistances_(R). Capacitors (0). 25,27 25K 19,30,31 .005 26 220K 20 .05 28,29,32 100 5w 21,22 .1 30 25K 100w adj. 23 300mmf var. 31 20K 100W 24 .0015 .001 2000V Transformer (T). 5 6 OBV-I'l 08amp 25,27,28,29 26 24 145-145 var. Tubes (V). Inductances (L). 9 6AG7 9 28 microh1 10 807 10 3 turns 4g" diam. 1/8" spacing ll VR 150 14 38 microh RFC 2,3,4 2.5 mh RFC 5,6 7.0 mh Receiver: Resistances (R). Capacitors (C). . 37,42,52,55 2.2Meg 37 lOOmmf 38 220 38 500mmf 39,44,58 10K 39,40,44,48 .001 40,45 81K 41,49 365mmf ganged var. 41,47 500K var. . 42 .05 43 470 43 .0015 46 30K 45 24 150V electrol. 48 39K 46 1.0 49 220K 47,50 .01 50 25K 51 800mmf 51 3.1K 52,53,54 16 450V electrol. 53 500K 54.59 470K 56 2.5K 5W’ Inductances (L). 57,60 450 5w 11,12 38 microh 61 45K 10w 13 14 hy 62 25K 10W RFC 7 2.5 mh 63 70 Tubes (V). Transformer (T). 12,13,14 6A0? 6 350-0-350, 5V-3amp, 6.3V-1.2amp 15 6SJ7 l5 VR 105 17 VR 150 18 80 19,20 6L6 All values of resistances in ohms, unless otherwise Specified, all values of capacitors in microfarad, unless otherwise specified. 25 IV.‘MECHANICAL EQUIPMENT The sound source consists of a crystal which is sup- ported by a holder of conventional design. For maximum output the crystal is air-backed. In all experiments des- cribod here a barium titanate disk was used. Fig. 13 shows the arrangement for the reflection meth- od. The tank holding the liquid is stationary, the left vertical wall is parallel with the crystal face and serves as the reflecting surface. The crystal holder is supported above the tank and can be moved through the liquid by a vernier, calibrated to 0.1 mm. If the instrument is used for transmission measure- ments, a second transducer, identical with the first one, is mounted on the supports on the left between the thermo- meter and the stirring motor. For experiments with liquids of temperatures higher than 50° a Pyrex dish replaces the glass tank, and a metal reflector is submerged in the liquid if the reflection method is employed. The crystal holder can be turned sufficiently around its three axes to hold the crystal in any necessary pos- ition. 26 Crystal Mounting . Fig. 13. 27 V. MEASUREMENTS As pointed out already measurements can be made either by the transmission or the reflection method. Ordinarily the actual distance between the crystals) (or between crystal and reflector) is not known. The trans- ducer is placed somewhere in the liquid, the reading of the mm vernier is recorded for this particular position, and the movable marker on the sweep of the CRO is placed on the be- ginning of the vertical deflection representing the first reflection. The time correponding to the position of the transducer is read on the sweep delay scale of the CRO. Then the crystal is moved some distance, either towards the second crystal (or reflector) or away from it. The readings are repeated for the second position, and the differences between the distances and the times are used to calculate the velocity of sound through the medium. In order to determine the velocity in solids only one reading is taken, and the actual distance between the crys- tals (or crystal and reflecting surface) has to be known. Fig. 14 and 15 show the difference for two readings in water. The crystal was moved through 50.0 mm; thus the difference between the second deflections represents the time reqired for the sound to travel 100.0 mm (reflection method). The first deflection is caused by the initial 28 pulse activating the transducer. Fig. 14. Short Path Fig. 15. Long Path Reflection Reflection If the absorption of the medium is not too high multip- le reflections become visible, and it is possible to use the second or third reflections for measurements. Fig. 16 shows a pattern obtained by using the trans- mission method. The first deflection is the amplified an- tenna pick-up, the second is the signal caused by the sound Fig. 16. Transmission Pattern 29 pulse reaching the receiving crystal. Some of the sound energy is reflected from the holder of the receiving trans- ducer, travels back to the transmitting crystal, is reflect- ed there and finally reaches the receiving crystal. Thus the third deflection is the trace of the sound pulse after it has crossed the medium between the crystals three times, the fourth deflection after five crossings etc. As pointed out previously measurements of absorption meet a fair amount of difficulties. Yet it is not impos- sible to obtain results, numerically too low, yet indic- ative. The attenuation box is placed between the receiv- ing transducer and the input of the receiver, thus the in- put can be attenuated in steps 0f 1 db to a total of 41 db. Measurements are made by observing the negative amplitude of one of the reflections, preferably the first one on ac- count of its relatively high negative deflection, and by noting the position of its lowest point. Then the crystal is moved closer to the second crystal (or reflector), and the deflection of the same echo becomes more negative (longer). Attenuating the receiver input decreases the amplitude, and the amount of attenuation needed to bring the deeper deflection up to the level of the first setting gives an indication of losses due to increased distance of the sound path. Galt15 has used essentially the same method of obtain- 50 ing absorption coefficients, yet there are three main dif- ficulties to be considered. First, since the output of the transmitter is tuned to the crystal frequency, the output stage will resonate with the crystal if it is activated by the sound pulse reaching it from the reflector. This means that not all the electrical energy generated by the crystal reaches the receiver but part of it is consumed in the out- put stmge of the transmitter. This loss varies with the impedance match between crystal and transmitter and between crystal and receiver input. Fig. 17 shows an extreme case where enough power reaches the output tank circuit to be Fig. 17. Vibrations in- duced in Transmitter visible on the CRO. This unwanted situation can be used for measurements of sound velocity in a very simple manner, name- ly by not having a receiver at all, and using the tank cir- cuit as detecting device. The second difficulty arises because the cross section 31 of the wave train constituting the sound pulse varies with the distance from the source, thus not the same cross sec- tion is intercepted by the second crystal (or the first af- ter reflection) at all distances, and as long as not the en- tire pulse is utilized in making absorption measurements, the measurement will be inaccurate. The third difficulty is caused by properties of the elec- tronic circuit. If attenuations are made to decrease the signal amplitude reaching the receiver, then the overshoot of the receiver amplifier caused by a strong initial pulse also decreases, and the base line, which is an.exponentially decreasing sweep from the end of the initial pulse, approach- es a more mearly horizontal position. Thus the pulse traces originating on the base line show a deflection minimum lower than they would have without attenuation and with a more curved base line. Fig. 18 illustrates this source of error. e - . __ _V w - - i cite/imam _ - __ T __ _. 1‘ {561’ any 2 ”4.561507; afar Mada/(2m Fig. 18. Effects of Attenuation Therefore only velocity measurements are included here since they do not depend on above mentioned phenomena. 32 VI. EXPERIMENTAL RESULTS A. Calibration Before any velocity readings of the substances to be examined could be taken the instrument had to be calibrated and checked for consistency; therefore a few preliminary measurements were made in liquids with a known change of sound velocity as a function of temperature. Then sound velocities were measured in liquids which are not suspected to exhibit any abnormal behavior, like tap water and motor oil. Fig. 19 shows some 0f the results, the readings ob- /560 M90 7 Wafer -\.: §~ , egg-1 L 0 $540 1400 s e / “3‘ g , 5.4.5 40 oh; \E m . a 534“” .Sfliiaflad \\\\\\%\\\ [snag § 3 a K 5% HML r /240 20 40 60 80 7enyxya£afle WC Fig. 19. Sound Velocity in Water and Oil 33 tained for distilled water did not differ by more than 0.1% from the values given by Masonl6. S.A.E. 20 motor oil was compared with S.A.E. 40 oil which was examined by Melchor and Petrauskasl7. B. Measurements It was hoped that a pulse generator might be an ins- trument delicate enough to show experimentally whether some liquids cause a dispersion of sound velocity which is not due to temperature changes but to either changes of frequen- cy or changes in sound intensity. Bergmann18 lists a number of researchers who conducted experiments designed to show the existence of velocity dis- persion; only fractions of 0.1% dispersion could be detected. Hueter and Bo1t19 state that at attainable frequencies the dispersion is ordinarily so small that it is not measurable. Yet experimental evidence of dispersion was offered by Mas- on et aleO who investigated polymers of isobutylene. Also Ghurevitch21 mentions experiments performed in 1938 proving that acetic and formic acid show frequency-depending dis- persion. Other workers found a dispersion of sound veloc- ity in rubber4 and a few other substances with high molec- ular weights22. However, none of the papers mentioned demonstrate any velocity dispersion as a function of sound intensity, a1- thoueh it was suspected23. until Wade. Simbo, and Ode21+ 34 published their findings of frequency dependence of sound velocity in fatty acids, including one case of intensity dependence. Thus it was considered interesting to investigate the dependence of sound velocity on sound intensity in lauric, palmitic, and stearic acid. Fig. 20- 22 show the results of this investigation. The sound frequency used in all ex- periments was 2.595 M0, the transducer a disk of BaTi03 which has the pr0perty of decreasing its output intensity at higher temperatures, yet in the range covered this de- crease is smallls. The only influence a change of BaTiO3 can have on the results would show as slightly too low vel- OCity readings in the vicinity 0f 810 and above. It is possible to repeat the experiments at different frequencies without replacing the transducer since BaTiO3 responds to all frequencies within a wide range25; however, this change to a different frequency would quite naturally involve a change in the intensity of the sound output, and since it was found that sound velocity depends on both the frequency and intensity, it would be impossible to differ- entiate between the additive effects of both changes. This impossibility arises from the fact that the sound pulses are so short that no instrument could be found to measure the actual intensity of a single pulse. I280 X 60 a / N O .5on Velocity m/sec. IZOO 80 \. 40 .50 60 70 Tempe/draft °C Pea/A {o — peak daring Voltages; x 90 volt o 70 volt A éETwafi‘ Fig. 20. Velocity Dispersion in Laurie Acid 36 60‘ 0\ Q Sou/7d Veloazv 07/566. 8 0 / 8 2" .MMO \\ 60: 60 70 60 @mperczfare °C 0 90 volts x 70 volts Fig. 21. Velocity Dispersion in Palmitic Acid 37 /’// , 7 k) 0 I200 \\ .Somd Veloci'é/ m/sec‘. so \\ 60 \__+ 60 70 so 90 femperalzzre ‘0 x 90 v0 [1‘5 0 70 volts A 55 volts Fig. 22. Velocity Dispersion in Stearic Acid 38 By using the same transducer at a fixed frequency it becomes convenient to express the relative intensity chan- ges in peak-to—peak voltages with which the crystal is driv- en. Different crystals will not yield the same sound inten- sity, even if supplied with the same voltage. Therefore no attempt was made to confirm wada's results concerning frequ- ency dependence. Fig. 23 indicates the results of an investigation made to determine whether the velocity dispersion in fatty acids is due to only frequency and intensity changes. Palmitic acid was used since it shows the greatest dispersion. Points L on the curve were obtained by transmitting sound pulses of 47 microseconds duration, points 8 by using pulses of 19 microseconds; in both cases the driving voltage rem-‘ ained the same. Considering that the ratio between the pulse length is about 2.5, and comparing it with data in Fig. 22 where the intensity ratio between the two curves is about 1.65, the results seem to indicate that velocity dis- persion is not due to a change in total energy (pulse length) radiated into the medium but only to amplitude variations (pulse height), the frequency remaining constant. The dependence of sound dispersion on sound intensity does not fit into the general scheme Of a linear relaxation theory. For constant temperature Nada observed a dispersion curve showing a resonance type behavior: the sound velocity 39 / \ .S \ \ 1 E5 Sound Veloaly 07/586 /20 \ L ' \ //80 60 7O 80 fifiqpenmmvr”%7 Rzlmlflc Add 80 volts Pulse Length: .3 . .. /9/u¢ec. L ...... 47/usac. Fig. 23. Effects Of Increased Pulse Length 40 increases with increasing frequency to a peak value and then decreases again. This special type of dispersion has been predicted in the unified relaxatiOn theory given by Hiedemann and Spence26 for the case that a substance is present in two different phases. This agrees with the explanation offered by Wada that near the melting point fatty acids may contain certain groups with a higher state of order than the rest. By means of a rather formal approaeh‘wada succeeded in der- iving a dispersion formula predicting a dependence of dis- persion on sound intensity. Wade. himself, however, pointed out that this theory does not give a physical explanation of the relaxation.mechanism involved. It may be significant that recent work27 has proved the existence of a liquid crystal state in derivatives of the fatty acids (sodium stearate etc.). Investigations of ultrasonic dispersions in liquid crystals will show if these effects can be used as indicatOrs for the liquid crystal state 0r also for a lower state of order. 41 VII. SUMMARI The usefulness of a radio-frequency pulse generator was demonstrated. The possibility to change various char- acteristics of sound output allows a great number of in- vestigations.to be carried out with the instrument. It was shown that the apparatus is not limited to sound vel— ocity measurements in liquids which.were described. DiSpersion of sound velocity in three fatty acids was shown to exist; it was found that this phenomenon is a func- tion of sound intensity and not of total sound energy rad- iated into the medium. 42 2. 3. 4. 10. 11. VIII. BIBLIOGRAPHY Hiedemann, E. "Wellenausbreitung in festen KBrpern, Ultraschall", Fiat Review of German Science, Physics of Solids (1947). Firestone, F. A. U.S. Patent 2,280,226 (1942). Teeter, Jr., C. E. "AbsOrption of Supersonic waves in Liquids", J. Acoust. Soc. Am., 18, 488 (1947). Ivey, D. G., Mrowca, B. 1., Guth, a. “Propagation of Ultrasonic Bulk waves in High.Polymers , . Appl. Phyflo, 20, 486 (1949). Lutsch, A. "ZerstBrungsfreie Prflfung durch.Uberschall mit dem Laufzeit-Echoverfahren", Arch. Eisenhttw., 23! 57 (1952). Seemann, H. J., Bentz, W. "Untersuchungen.flber den Ein- fluss des Gefflges auf die Extinktion von Ultraschall- wellen in metallischen Steffen", Z. Metallk., 45, 663 (1953)- Lutsch, A. "Eine einfaehe Methods zur Messung der elast- ischen Konstanten mit Hilfe von Ultraschallimpulsen”, Z. ang. Phys., 4, 166 (1952). Termann, F.E., Pettit, J. M. "Electronic Measurements", MeGraw—Hill, New York (1952). Ficken, G. W. "A Sing-Around Circuit for the Measurement of Sound Velocity , Master's Thesis, Michigan State College (1953). "Radar Electronic Fundamentals", NAVSHIPS 900,016, Navy Department, Washington, D.C. (1944). Elmore, W.C., Sands, M. "Electronics", McGraw-Hill, New York (1949). Easton, A. "Pulse Modulated Oscillator", Electronics, MflPCh 1947. "Radio Amateur's Handbook", 32nd cd., ARRL, west Hart- ford, Conn. (1955). Martin, Jr., T. L. "Ultrahi h Frequency Engineering", Prentice Hall, New York 1950). 43 15. 16. 17. 18. 19. 20. 21. 22. 23. 27. Galt, J. K. "Mechanical Properties of Alkali—Halide Crystals", M. I. T. RLE Techn. Report 45 (1947). Mason, W. P. "PiezOelectrie Crystals and Their Applic- ation to Ultrasonic", Van Nostrand, New York (1950). Melchor, J. L., Petrauskas, A. A. "Ultrasonic Studies of Polymethyl Methacrylate", Ind. Eng. Chem., 44, 716 (1952). Bergmann, L. "Der Ultraschall und seine Anwenduni in Wissensehaft und Technik", Hirzel, Zfirich (l9 9) Hueter, F., Bolt, R. H. "Sonics", John Wiley & Sons, New York (1955). Mason, W. P., Baker, W. 0., MCSkimin, H. J., Heiss, J. H. "Mechanical Properties of Long Chain Melecule Liquids at Ultrasonic Frequencies", Phys. Rev., 73, 1074 (1948). Ghurevitch, S. B. "Absorption of Ultra-Acoustic Waves in Liquids", C. R. (Doklady) Acad. Sci. URSS, EV. 17 (1947)- Ballou, J. w., Smith, J. c. "D amic Measurements of Polymer Physical Properties', J. Appl. Phys., 20. 493 (1949). Seidl, F. "Schallabsorption in beschalltem Transforma- toren81", Colloquium Over Ultrasonore Trillingen, Koninklijke Vlaamse Acad. voor Wetenschappen van Belgié (1951). Wade, Y., Simbo, 5., Oda, M. "Dispersion of Ultrasonic Velocity in the Liquid Fatty Acids", J. Phys. Soc. Japan, 5, 345 (1950). Schaaffs W. "Sehallgeschwindigkeit und Molekfllstruktur in Flflssigxeiten", Erg. ex. Naturw., xxv, 109 (1951). Hiedemann, E., Spence, R. D. "Zu einer einheitlichen Theorie der Relaxationserscheinungen", Z. f. Phys., 133. 109 (1952)- Moses, H. A. "The Proton Resonance Absorption in Liquid Crystals", Master's Thesis, Michigan State College (1953). 44