M86 iiiiiiiiiiii This is to certify that the thesis entitled A NEW EXPERIMENTAL METHOD FOR MEASURING WATER CHARACTERISTIC CURVES OF SOILS presented by Gholamreza Rakhshandehroo has been accepted towards fulfillment of the requirements for M.S. , Civil & Environmental degree in Engineering ajor professor Date ¢§A¢L 0-7639 MS U is an Affirmative Action/Equal Opportunity Institution LIBRARY Michtgan State 'I Untverslty PLACE IN RETURN BOX to remove this checkout from your record. TO AVOID FINES return on or before date due. DATE DUE DATE DUE DATE DUE A NEW EXPERIMENTAL METHOD FOR MEASURING WATER CHARACTERISTIC CURVES OF SOILS BY Gholamreza Rakhshandehroo A THESIS Submitted to Michigan State University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE Department of Civil and Environmental Engineering 1992 r 4") A A If. I cv/ C1, 79,; ABSTRACT A NEW EXPERIMENTAL METHOD FOR MEASURING WATER CHARACTERISTIC CURVES OF SOILS BY G. Reza Rakhshandehroo A new experimental method by which one can measure saturation as a function of capillary pressure in a soil sample was investigated. The method imposed a saturation on a sample and measured resulting capillary pressure. After each drainage increment a period of time was required for the sample to come to internal static equilibrium. In this paper, this was referred to as the "redistribution time". The effect of hydraulic gradient on both drainage time and redistribution time at different saturations was investigated. The results showed that data obtained by this new method and the traditional method agree. Increasing the hydraulic gradient when high saturations exist speeded the drainage up but increased the redistribution time. At lower saturations a higher hydraulic gradient retarded both the drainage and redistribution processes. Seven experiments determined the internal moisture profiles at the end of a drainage step which found not reproducible. It. was postulated. that 'the shape of such profiles depend on the internal microscopic structure of the sample. ACKNOWLEDGEMENTS First and foremost I would like to thank professor Arthur T. Corey for presenting his invaluable course in the mechanics of immiscible fluids in jporous media. His guidance and assistance to complete this thesis were also greatly appreciated. My sincere thanks to my major advisor Dr. Roger B. Wallace for his encouragement, support and patience throughout my thesis. Furthermore, I would like to thank the members of my thesis committee, professor David C. Wiggert and Dr. Susan Hasten. In addition, I wish to thank my office mates and friends who have made my study easier and my life more enjoyable. Finally I greatly thank my family. My father and mother have provided me with the motivation to continue my study. My wife has continuously encouraged me to complete my master's work. ii QHAEIEB TABLE OF CONTENTS LISTOF FIGURES ......OOOOOOOOOOOOOOOOO. LISTOF 8mm ......OOOOOOOOOOOOOOOOOO CHAPTER 1 INTRODUCTION ............................. m2 PROBLHSTATMT ......OOOOOOOOOOOOOOOOOO General Background ................................ Objecti Theory Physics ves ......OOOOOOOO......OOOOOOOOOOOO of The Problem .................... EQUIPMENT AND PROCEDURE .................. General Pressure Cell ............................. Burette Pressure TranSducer ......OOOOOOOOOOOOOOOOO Valves Set up 3.6.1 3.6.2 3.6.3 3.6.4 3.6.5 And Procedure ......OOOOOOOOOOOOOOO. Set up ............................. New Method Procedure for Determination of Pc(S) .............. Traditional Method Procedure for Determination of Pc(S) .............. Procedure for Determining moisture Profiles Within the Soil Samples ... Procedure for Determining the Influence of Hydraulic Gradient...... iii 10 12 21 21 21 24 24 25 27 27 28 32 34 35 CHAPTER 4 iv RESULTS AND DISCUSSION ................... General ....................OOOOOOOOOOO.... Water Characteristic Curves ............... 4.3 Moisture Profiles Within the Soil Samples .. APPENDIX REFERENCES Influence of the Hydraulic Gradient on the Drainage and Redistribution Times .. CONCLUSION AND RECOMMENDATIONS ........... 37 37 37 50 52 59 LIST OF FIGURES EIEUBE 1 Schematic of Experimental Apparatus .......... 2 Pressure Cell Schematic ...................... 3 Water Characteristic Curve ................... 4 Redistribution Time at Different Saturations . 5 Moisture Profile Within the Soil Samples ..... 6 Drainage Time Under Different Gradients ...... 7 Redistribution Time Under Two Gradients ...... A-l Calibration Curves 22 23 38 43 46 48 53 LIST OF SYMBOLS flux through a unit cross sectional area; [L/T] hydraulic conductivity; [L/T] hydraulic head; [L] distance from the origin in the direction of flow; [L] ”I." :3 NH, radius of curvature of the interface; [L] a interfacial tension; [F/L] P; capillary pressure across an interface; [F/L’]. V output voltage; [v] IL capillary pressure head; [cm of water] vi CHAPTER 1 INTRODUCTION Water flow in soil is of great importance to engineering, 'hydrology’and.agriculture. The laws under which water flows in fully saturated soil have been studied extensively' both experimentally and theoretically, however, flow in unsaturated zone needs more study. In the unsaturated or vadose zone, soil water content depends on the difference in water and air pressure within the soil. In the vadose zone, water pressure is usually less than that of the air. The greater the soil water content, the smaller the difference between air and water pressures. The functional relationship, however, depends on the type of soil and is also subject to hysteresis. Curves depicting water content (or saturation) as a function of pressure difference (between soil air and water) are called "water characteristic curves". These curves can be obtained. either through a drainage or wetting cycle. Starting with fully saturated soil (with water) and decreasing the soil water content successively completes a drainage (or drying) cycle. The wetting (or inhibition) cycle, on the other hand, requires 2 addition of water to initially dry soil. These curves are also called "water retention" or "capillary pressure vs. saturation" curves. This thesis presents results Vof experiments which generate water characteristic curves for a given soil sample using a different method than those traditionally employed. The "pressure equilibrium" method, which has not been previously studied with this design and accompanying simple procedure, is reported and the results are compared to the traditional method of generating data. The basic concept of this neW'method is to impose a known saturation on the soil sample and measure the resulting pressure difference under a static fluid (no flow) condition. The set up is designed to make the overall measurements faster. The use of a reluctant pressure transducer and associated electrical instruments makes the pressure difference measurements more reliable. A modified pressure cell technique is employed so that the size of the sample is relatively small and changing the sample saturation requires removal or addition of less wetting phase. This thesis is divided into five chapters and an appendix. Chapters 2 and 3 present theory and experimental procedures used in this study, respectively. Comparison of results obtained from different equilibration techniques, as well as details of this new method, are presented in Chapter 4 of the thesis. The last chapter contains conclusions based 3 on the results and some recommendations for future work. The Appendix contains the procedure to calibrate the pressure transducer along with some data and also a list of apparatus components with names and addresses of parts providers. CHAPTER 2 PROBLEM STATEMENT 2.1. General Water characteristic curves have been generated by many investigators using a variety of different laboratory techniques. Topp, etmal. (1967), havercompared.curves obtained by different methods and have shown that the results are dependent on the state of flow of the water. However, it is a common practice to use the water characteristic curves obtained under static condition of fluids in most cases. This chapter presents a review of traditional methods for developing water characteristic curves along with a brief explanation of the new apparatus and approach employed in this study. This is followed by the objectives of this work. The theory and the physics of new system are described at the end. 2.2. Background Richards published the first plots of water characteristic: curves, in 1928. These curves ‘usually’ are determined on samples by changing the pressure difference across the air-water interface (the capillary pressure) in 5 increments and letting the water content adjust until equilibrium is achieved. The apparatus used to make such measurements is called a "pressure cell". The pressure cell was first described by W. Gardner et a1. (1922). The pressure cell method involves placing a soil sample in contact with a "pressure plate" or capillary barrier and controlling water and/or air pressures. The pressure plate is an essential component of a pressure cell. It is a porous plate made of glass, ceramic or a thin sheet of metal. In any case, the pressure plate has very small pores so that, when saturated, it allows only water and not air to pass through its pores over a range of capillary pressures chosen to study the saturation characteristics of the soil sample. The pressure difference at which air breaks through the plate is called the bubbling point or air entry pressure. Hence, any pressure difference less than the bubbling point applied across the plate is transmitted to the soil water in the cell. This feature of the pressure plate provides an efficient way t0.~> o>_m> EBA.” cozeamwéaaog to mE 0 852558 a a. > 8:th m>_m> 325m \ t D .8335... § 8335 .6233. =8 ._o=_om 8:365 3325 538052 , .825 I m>_m> ._< _ Eozusm . v 9:305 .3 ch 23 To Air Pressure (or Suction) ‘ ‘ Top Cap Outer ’/ Cylinder \ ‘— \ Inner Cylinder Sa I mp e \ Screw Filter Paper N 0 II It rings Pressure /— Plate liottom ,_LJ Cap To Burette and Transducer Figure 2. Pressure Cell Schematic 24 to transmit suction to the soil water. Two O-rings on the top and bottom of the pressure plate along with the epoxy provided a seal, while on the top of the cell a single O-ring was used. A paper filter placed on the topiof plate prevented clay-sized particles from entering the plate. Side screws were provided to fix the inner cylinder relative to the outer one in order to permit the bottom seal to be achieved before packing soil into the cell. 3.3. Burette A glass, 25 ml burette with a bottom stop cock and 0.1 m1 graduations was used during the experiment. The stop cock was a high quality, zero-displacement valve. It was used to stop and start the drainage in order to impose known saturations on the sample. Thick-walled Teflon tubing was usedto connect the burette to the cell and transducer, Figure 1. The liquid content of the sample was monitored volumetrically using this burette. 3.4. Pressure Transducer The most critical device used in the experiment was the pressure transducer and its associated components. A very sensitive variable reluctance pressure transducer was used (model number CJVR, C.J.Enterprises, Tarzana, CA). It was designed to measure low and medium gage, as well as, differential pressures. Using a carrier demodulator and 25 voltmeter, the transducer produced a 0 to :10 volt DC output in response to a 0 to maximum pressure difference on its diaphragm. A brief technical description of the transducer from the manufacturer's manual states: "The transducer consists of basically a flat pressure sensing diaphragm (field replaceable) clamped between two matched case halves each containing electrical pick off coils. Applied pressure deflects the diaphragm which is detected by the two pick off coils. When the coils are connected as two opposing legs of a bridge circuit, the resultant bridge output is proportional to pressure. Bleed screws are provided in both case halves to facilitate . complete liquid filling for dynamic measurements." The pressure transducer was connected across the ends of the cell. One port was always filled with Soltrol, whereas, the other port was connected to the air source as shown in Figure 2. This pressure measurement reflects the pressure difference between air and Soltrol i.e. the capillary pressure, .P , across the plate. C A calibration curve was frequently developed to convert output voltage into pressure difference. Characteristics of the transducer and other related electrical devices were investigated and shown to be satisfactorily stable. A typical result is discussed in the Appendix. 3.5. valves Besides the burette valve, which, was previously 26 described, three other valves were used in the system (Figure 1). They are referred to as the 3-way valve, air valve and vacuum saturation valve. The vacuum saturation valve was used for initially saturating the plate and the soil. It had two important characteristics. First, it was capable of providing adequate seal when a relatively high vacuum (around 700 millibar) was imposed on the air phase at the top of the cell to take the air out. Secondly, it was a displacing valve (not a desired characteristic) that was capable of a fairly fine regulation of valve opening and therefore liquid flow. With this valve, the Soltrol inflow to the cell to initially saturate the sample was kept to a reasonably low rate. This was judged necessary as a relatively high inflow rate could have changed the internal structure of the packed sample, especially at the unrestrained top surface of the soil. The internal volume of this valve was measured and accounted for during the experiment. Once the sample was saturated, the vacuum was released and this valve was left open for the rest of the experiment. The air valve was a three-way stopcock. It had.a rotating core with T-shape opening. It connected all three air lines during the experiment. In order to initially vacuum saturate the sample, this valve was set so that the suction was transmitted only to the cell. During the calibration, however, the air pressure was applied only on the transducer through this valve. 27 The 3-way valve on the liquid side was a 3-way ball valve with directional flow switching. It had an inlet port that could.be connected to either'of the other two ports. The inlet port was connected to the transducer. During the experiment this valve was positioned so that the transducer'was connected to the pressure cell. For calibration purposes and during the initial vacuum saturation of the sample, the valve was used to, isolate the cell and connect the transducer to the constant pressure head Soltrol reservoir. The calibration setup and procedure are discussed in the next section. 3.6. Set up and Procedure 3.6.1. Set up The procedure used here, as discussed before, is a variation of traditional pressure cell technique. The main differences are: 1. A desired saturation is imposed on the sample and the resultant capillary pressure is measured, as opposed to the traditional method that leaves the soil under a constant capillary pressure to come to saturation equilibrium over time. 2. A pressure transducer along with a carrier demodulator and voltmeter are used to monitor the capillary pressure. The setup allows a quick, reliable measurement. 3. An aluminum cell is used to minimize the effect of 28 diffusion through the cell body. These differences enable the investigator to obtain the whole water characteristic curve in a more convenient manner than with other static devices and procedures. The design allowed data to be obtained both by this new method and the traditional method. Figure 1 shows the setup schematically. The transducer was wired to the carrier demodulator and a voltmeter. It had a sensitive replaceable diaphragm and because of the type of soil sample a 0-1 psi diaphragm was employed. The demodulator was set so that the output signal had the maximum. possible value when the transducer ‘was subjected to the maximum pressure difference. By setting the controls on the demodulator, a 0-10 volt output was registered on the voltmeter when the transducer was subjected to its full range of pressure differences. By locating the transducer at the same elevation as the midpoint of the sample, it directly provided capillary pressure corresponding to the mid sample position whenever the fluids were static. 3.6.2. New Method Procedure for Determination of Pc(S) The general procedure was to remove a specified volume of water from the soil and measure the resulting capillary pressure. The drained volume was determined with the graduated burette and the saturation was calculated. The capillary pressure was measured with the pressure transducer which was connected to a voltmeter. The voltage signal was registered on 29 the voltmeter and.was converted to capillary pressure by using the calibration data. Vacuum saturating the space beneath the plate and the plate itself was the first step. The vacuum saturation valve was closed and the burette valve opened. An oven dried pressure plate was employed and the vacuum was created by applying 700 millibar air suction on top of the plate. Then the vacuum saturation valve was opened.to let Soltrol saturate the space and the plate. When the saturation process was complete the air suction was removed. Any air trapped inside the space was identified and removed by turning the cell over and applying a small suction on top of the burette. Then the burette valve was closed. A paper filter was placed on top of the pressure plate and the system was weighted. » A fine sandy air-dried soil was packed on the filter paper and plate: the soil had a free top surface. The packing device was a 20 cm long, 3 cm diameter tube with a 2 mm mesh screen at the bottom to help uniformly distribute the soil particles. The tube was placed on the plate, filled with the soil, pulled up slowly and rotated uniformly until the cell was almost filled up. The cell was dropped 10 times from an elevation of 3 cm. Then the free top of the soil was hammered by dropping a 1.5 kg weight 10 times from a 1 cm elevation. When the packing was complete, the system was weighted again and vacuum saturated, in place, within the cell. 30 Vacuum saturating the soil was almost the same as vacuum saturating the plate. As rationalized earlier, the vacuum saturation valve was used to insure a small flow rate of Soltrol during saturation. First the sample was over saturated. Then the high vacuum was removed and the vacuum saturation valve was totally opened. The system was left under a small hydraulic gradient for a long time so that excess Soltrol would drain out. The volume of Soltrol necessary to fully saturate the sample was monitored with the burette. It was corrected for the small volume added to the system by totally opening the displacement valve (vacuum saturation valve) and was considered to be the total pore volume. At the end, the pressure transducer along with the Soltrol reservoir and other electrical devices were connected to the system as shown in Figure 1. I Before starting the experiment, the transducer was calibrated. It was also frequently calibrated in place during the experiment. Calibration was achieved by positioning the air valve and the 3-way valve in Figure 1 such that the pressure cell and burette were isolated from the transducer. Transducer calibration was accomplished by controlling the regulated air pressure on one side of the transducer and connecting a static Soltrol reservoir to the other side. Data for calibration were obtained by progressively increasing the air pressure on the transducer and decreasing it.back to zero. Air pressure was monitored with a U-tube water manometer. The 31 accuracy of the calibration procedure is discussed in the Appendix.‘ The drainage branch of a water characteristic curve was initiated by positioning the air valve so that air pressure was applied to both the transducer and the cell. The 3-way valve was set to connect the transducer to the cell and isolate the Soltrol reservoir. With the burette valve closed, relatively high air pressure was applied to the top of the cell. Soltrol was then allowed to drain.out of the sample into the burette under a relatively high pressure gradient by opening the burette valve. When the desired volume of Soltrol was drained into the burette, the burette valve was closed again. Saturation of the sample at that point was calculated from the known Soltrol drainage and the initial Soltrol volume in the pore space. Output voltage was read on the voltmeter and converted to capillary pressure by using the calibration curve. The process of desaturating the sample and measuring capillary pressure and saturation went on by opening and closing the burette valve and reading the voltmeter and burette. Smaller drainage increments were employed where the water characteristic curve exhibited large values of dS/ch. Once a specified volume of Soltrol was drained out.of the sample, a period of waiting was required for the system to equilibrate (redistribution period) before additional Soltrol was drained. During this time Soltrol was not allowed toidrain 32 out, but the voltage signal on the voltmeter was observed to drop to some stable value asymptotically. As rationalized earlier, this transient time was attributed to the redistribution of the moisture inside. the sample. In this study, the ‘time required for ‘voltmeter stabilization is referred to as "redistribution time". During redistribution, the voltage was recorded periodically until it approached a stable value. However, the length of time required to achieve internal equilibrium was not well defined because it is approached asymptotically. Furthermore this time was observed to depend upon saturation. Therefore, the actual time recorded as necessary to achieve redistribution was dependent on the operator's judgement. In this study the voltage was recorded for a long time after each drainage step to insure that most of the change in capillary pressure had occurred. Despite the subjectivity associated with the determination, a consistent criteria was used throughout the experiments. 3.6.3. Traditional Method.Procedure for'Determinationiof p43) The second objective of this study was to compare the results obtained by this newrmethod.and'the traditional method quantitatively. To achieve that, in between the new method points and within the same run, some data were collected by allowing the sample Soltrol saturation to equilibrate under an 33 applied pressure difference. The procedure was as follows: The drainage curve was. developed. by increasing air pressure to its maximum value in four steps. Within each step, data were obtained using the previously described procedure. At the end of each step the burette valve was left open for a relatively long time so that the soil sample could drain to equilibrium under the imposed pressure difference. Then a single data point was recorded that was based on the traditional method. An indication of the occurrence of true equilibrium was obtained by shutting the burette valve off and determining that no significant change on the voltmeter could be observed. This would occur if no outflow'had.been occurring when the valve was closed which indicated, by definition, that equilibrium existed. By this technique, data were obtained using both the traditional method and the new method on a drainage cycle. At the end of each experiment the Soltrol mass balance was checked by oven drying the sample. In addition, the transducer was recalibrated. Comparison of before and after calibration curves show sufficient consistency in basic characteristics of the electrical devices used in the experiment. The Appendix includes a set of such curves. Although only drainage cycle curves were generated in this study wetting cycle curves could have been measured. These would be initiated after the Soltrol was brought to residual saturation on the drainage cycle. 34 3.6.4. Procedure for Determining Moisture Profiles Within the Soil Samples To achieve the third objective seven experiments were conducted.to:measure the moisture profile within the sample at the end of a drainage step. The air valve and 3-way valve were positioned to isolate the transducer and the Soltrol reservoir since no measurement of the capillary pressure was needed in these experiments. The soil was packed and vacuum saturated in the same way as explained earlier. The soil sample was brought to a fully saturated condition while the saturation was monitored by the burette. At this time the burette and vacuum saturation valves were fully open. Desaturation of the sample was initiated by applying 70 mbar air pressure to the top of the cell. As a result, Soltrol was driven out of the soil under a relatively high hydraulic gradient. When the Soltrol saturation was reduced to approximately 0.5, the burette valve was closed and the air pressure reduced to atmospheric. The soil sample was stratified into three layers. Each layer was divided into three smaller samples. The samples were weighted, oven dried and weighted again. The Soltrol saturation of each sample was computed and a coarse moisture profile developed. In addition, the total saturation was checked by the mass balance. The stratifying process was conducted as quickly as experimentally possible to minimize internal moisture redistribution during this process. On average, 95% of the 35 mass of soil samples was collected and oven dried for saturation determination during the stratifying process. 3.6.5. Procedure for Determining the Influence of Hydraulic Gradient The final set of experiments measured the drainage and redistribution times at different saturations under two different hydraulic gradients. These experiments were performed using the new method procedure except that the air pressure was periodically adjusted in order to maintain a constant hydraulic gradient. Two soil samples were packed and vacuum saturated as explained earlier. The transducer was connected to the system and calibrated before running the experiment. With the burette valve closed, the air pressure was applied on top of the first sample so that the voltmeter registered 2 volts. By opening the burette valve, Soltrol was allowed to drain out of the sample into the burette. During the drainage increment, the air pressure was adjusted so that the voltmeter remained stable at 2 volts. The time required to drain the required volume of Soltrol was monitored with a stopwatch. At the end of the drainage step, the redistribution time was determined. The experiment continued by progressively desaturating the sample until the times required became too large. The second sample was subjected to a 4 volts gradient during the drainage. Except for this, it was desaturated in 36 the same way as the first sample. The drainage increments were the same in both cases. CHAPTER 4 RESULTS AND DISCUSSION 4.1. General An example of a water characteristic curve on a drainage cycle obtained. by the procedure previously' described is presented in this chapter. The results of the supplementary experiments and the drainage time measurements are presented next. The last section includes a general discussion on the redistribution process in the new method and the results of the redistribution time measurements. 4.2. Water Characteristic Curves A typical water characteristic curve obtained by the described procedures is shown on Figure 3. Solid squares represent data from the traditional method, where open squares are data recorded by the new method. The wetting phase saturation of the sample is shown on the horizontal axis and the capillary head in centimeters of water is on the vertical axis. The data were obtained on a single drainage cycle experiment on one packed sample. Soltrol was used as the wetting phase and air as the non wetting phase. 37 I323 £35.62 30 I .5562 >32 2 VIII. 'Illl'l 'II .....m l 'l‘.,' 3.: m- Tim -E i $-34 m LYIIIII ‘luitl, 6?. :0 053.230.3625 scoot m 939.1 I c ..n. .. .. a. _ ..m" Cu. 3’11 IC)ZZIII' 1351‘) 39 The probable error in values of He resulting from uncertainty in the calibration, is represented by the height of the squares. The contribution to this error due to the uncertainty of the true end of redistribution is not shown on the figure. This error was partly discussed in the last chapter and. will be discussed further in the following section. The inconsistency in the data especially at very low saturations could be mostly the result of the subjectivity in identifying the true end of redistribution. As shown in Figure 3, data from both methods appear to fit on a single smooth curve. This indicates that the water characteristic curve obtained by this new method has the same characteristics as the old curve and therefore such a curve could have the same applications as the traditional one. The data denoted by numbers are those for which data in the form of voltage as a function of time were collected during the redistribution period. The fact that the voltmeter did not register a constant stable voltage at the end of a drainage step is shown in Figure 4. This figure shows the voltage history at 5 saturation points. These points are labeled in Figure 3. The vertical axis is the voltage registered on the voltmeter at any time. The horizontal axis is the time that the voltmeter was monitored. Note that during these transition periods the drainage had been stopped by closing the burette valve (Figure 1) and the soil system was under an external static condition. 40 n b v x a o m . _ D 3.3: 65:. cvm com cc. om— on cw c — Ii'lllliriliiiu .IIIIi XIIXIIIXIIX I iifrt I 21/ ‘IIID. %.l./Ililf /W /’.L r/ €025.5an 6.2—0 do 68: Gofisfisamsom .V 9.39... c— afienoA (3104) 41 The voltmeter sensitivity' was one 'millivolt. It is equivalent to less than 0.1 mm of water when converted to pressure head. This level of accuracy was more than adequate for the system under consideration. Thetime was also measured accurately with a stopwatch. Therefore the margin of error in the data shown in Figure 4 is probably less than 1% in all cases. The main difficulty in analyzing the redistribution process is associated with the definition of redistribution time. It is the time required for the voltmeter to become "stable". As shown in Figure 4 the voltmeter drops to a final value asymptotically. Therefore, in a certain sense it will never become "stable" as it only becomes stable as t~w. Figure 4 shows that in some cases the rate of the drop is smaller and therefore it takes longer for the voltmeter to stabilize. One may conclude that the data determining the redistribution time and therefore the corresponding voltage at those cases are less accurate. Note that during the main experiment a long time was considered for the voltmeter stabilization at each point. The attempt was to capture the voltage drop as much as possible. Figure 4 shows that at low saturations the redistribution process is slower. In other words, it takes longer for the system to come to an internal static condition. It seems that the low conductivity and relatively large drainage increment could cause the delay. On the other hand at high saturations, 42 especially with small drainage increments, it is on the order of minutes for the redistribution precess to take place. Again the high conductivity there, could be the main reason for this behavior. . The voltage drop, by itself, shows that the capillary pressure across the cell is dropping. Noting that a constant high air pressure was applied on top of the cell, Figure 4 reveals that the wetting phase pressure:in the plate increases during the redistribution process. It confirms the physical analysis of the behavior of the system during the redistribution process presented in Chapter 2. 4.3. Moisture Profiles Within the Soil Samples The data from seven experiments are shown in Figure 5. The vertical axis represents the height of the soil sample which was divided into three equal layers. Layers 1, 2 and 3 refer to the bottom, middle and top layers, respectively. Each moisture profile in this figure depicts the saturation of the various layers of a particular packed soil sample after it has been drained from 100% to around 50% saturation in one step. As described before, three smaller samples were collected at each layer. It was observed that of all possible moisture profiles in a packed sample the vertical moisture profile was the dominant and more consistent one. Therefore, the average saturation of the three samples for each layer is shown in Figure 5. Saturation of the samples at each layer is provided we so mm sores—sum es ov mm 43 ii. 191(8'1 D w usur— 44 in the Appendix. As mentioned earlier, an average of 5% of the mass of the soil sample was lost during the stratifying procedure. The average saturation error associated with the data shown in Figure 5 is i0.8%. It was computed from the mass balance check at the end of each experiment by oven drying the samples. The layer’s heights were chosen to be equal in each soil sample. The average error in layer height is i3%. To analyze the profiles shown in Figure 5 let us first discuss why some regions in a single sample have higher moisture contents than other regions. According to the physics of the flow, the drainage will first occur locally along the path of least resistance. This path possibly includes the biggest pores that are filled with the wetting phase at the time. It is reasonable to believe that.in.a packed soil sample these paths and pores are located randomly. By the above analysis the inconsistency between the saturation profiles of different samples, shown in Figure 5, could.be rationalized- The profiles in this figure reveal that the drainage process within different samples occurs preferentially from different regions. These regions seem to be located in the samples without any consistent order. The reason could be the fact that each packed soil has randomness with regard to positioning of the pores and the least resistant paths. It is a microscopic property of a particular packed soil and can not be repeated by following the same 45 macroscopic packing procedures. 4.4. Influence of the Hydraulic Gradient on the Drainage and Redistribution Times 1 Figure 6 depicts the results of the experiments on the drainage process. They measured the drainage time for equal drainage increments under two different hydraulic gradients. They were performed on two different samples. Hydraulic gradients are given in volts which can be converted to the differential pressure head using the calibration curve. The time to drain the sample from a higher to lower saturation has been plotted at the lower saturation on the vertical axis. Drainage time was measured accurately using a stopwatch which recorded time to the nearest hundredth of a second. The saturation was monitored by the burette. The maximum error in saturation due to propagation of the burette reading error was 10.5%. The mass balance was checked at the end of the experiment by oven drying the sample. The measured error was -2% saturation. The loss was probably due to Soltrol that remained on the surface of the cell. As shown in Figure 6, at high saturations the wetting phase will drain.out.more quickly under higher gradients. This is consistent with the expectation based on Darcy’s equation presented earlier. At high saturations an average conductivity could be assigned to the entire sample. Then, neglecting conductivity variation over time and space, the drainage flux 46 .> v n 2325.5 + .> m H gag—coho D Jaw “no m6 m6 —.o g} .../«1; r. H JUNE. ... \«mwie 3:355» 9:98:20 .83.: we: owosgn m 939..— -. cm Cw. cm cc oc— om— cw— om: on: com Gem °1d am 01 163 01 sum. ('urw) 47 out of the sample is directly proportional to the hydraulic gradient. At low saturations, however, Figure 6 shows that the higher gradient retards the drainage process. The reason could be explained by considering conductivity variations inside the sample. As discussed earlier, drainage occurs in some regions of the sample first. Applying a high gradient could desaturate these regions considerably. Therefore conductivity of the sample would locally drop to a low value. Further drainage from the sample may require flow of the wetting phase through this region. In this situation the low conductive region would delay the overall flux out of the sample. Results from the experiments investigating the redistribution time are depicted in Figure 7. The figure shows the results on two packed soil samples each drained under a different hydraulic gradient. The vertical axis shows the redistribution time. The saturation of the sample is on the horizontal axis. Since the redistribution occurs when a fixed saturation exists in the sample, unlike in the case of drainage time, the redistribution time is assigned to a saturation point. The packed soil samples used in this last study were those used to develop Figure 6. The drainage and redistribution times were recorded on the same samples in a single run. Therefore, the errors associated with the measurements of the time and saturation are the same as 48 $6 .> e n Scam—5.5 + Jam .> m u 5:23.20 3 96 —.c h lmi I/T\\\V 3:253» 35 some: 083 :03355363— h 830E ow on co co— om— ov— om— cc— com. cum com owm emu. nonnqrnsmaa (mm) ' 49 discussed with regard to Figure 6. However, the determination of the redistribution time has an inherent uncertainty due to its indeterminate character by definition. This was discussed earlier in the last section. I In Figure 7 for saturations greater than 30%, data for the two gradients can not be significantly distinguished from one another due to the margin of error associated with each one. However, since the redistribution time measurements were conducted consistently throughout the experiment, one may draw a conclusion from those data. For example, it may be interpreted that the higher gradient causes a longer redistribution time, in general. At low saturation, the higher gradient causes such a longer redistribution time that the conclusion is obvious and undoubted. The behavior of the system during redistribution (Figure 7) may be deduced from Darcy's equation in a similar way to what was done with regard to drainage (Figure 6). The only difference is that the drainage is a process in which the wetting phase flows out of the soil sample where the redistribution process considers internal flow of the wetting phase. However, both processes are governed by the same concepts and equations. Note that the drainage increment may have an effect on the drainage and redistribution time under any gradient. This effect was not considered in this study. CHAPTERS CONCLUSION AND RECOMMENDATION C 5'0 5: Consistent results could be obtained by the new method by applying the explained procedures. Water characteristic curves obtained by the new method agree with the traditionally generated data. By' using' more controls, this method. generates more reliable results more easily, compared to previous methods. The controls include valves to set the saturation , a pressure transducer to track Pc , and capability to alter the hydraulic gradient. The new' method could require less overall time to generate Pc(S) curves, by using the controls. Very accurate measurements of capillary pressure are made by using a sensitive pressure transducer. The method establishes the external and internal static equilibrium conditions at two separate stages. Once the external static condition is imposed on the system,an internal moisture profile exists inside the soil sample that. may not. be at static equilibrium condition. The exact shape of such profile may depend on the internal structure of the sample and may not be reproducible through same packing procedures. The method requires a waiting period for the internal moisture to redistribute. Redistribution of moisture inside the sample is necessary for establishing the internal static equilibrium condition. 50 51 The hydraulic gradient causing the internal redistribution of moisture drops to zero asymptotically. Other things being equal, the redistribution time is longer at lower saturations. Results show 'that. at lower saturations, the higher hydraulic gradient retards both the drainage and redistribution. At higher saturations the higher hydraulic gradient makes the drainage and redistribution occur faster. The drainage and redistribution times may also depend on the drainage increments. MW Get the entire Pc(S) curve by the new method several times. Look for reproducibility of the curve. Determine the internal moisture profile at the end of drainage without destroying the soil sample. Look for reproducibility of the profiles. Try several hydraulic gradients to monitor the drainage and redistribution times at.different saturations. Look for the optimum gradient at every saturation. Apply suction on top of the burette to drain the sample. Look for any difference in the drainage and redistribution times compared to applying air pressure on top of the cell. Numerically simulate the drainage and redistribution processes. Compare the internal moisture profile at the end of drainage and also the drainage and redistribution times to experimental results. Look at the effect of drainage increment on the overall time to generate Pc( S) curves. APPENDIX APPENDIX During the course of the experiment, the valves and manometer were placed in the system.and.positioned.so that the set up could function for both the experiment and transducer calibration (Figure 1). The positioning of the valves is discussed in the set up and procedure section. Figure A-l shows two different calibration curves one obtained before and one obtained after an experiment that lasted two days. Pressure head difference across the transducer, in centimeters of water is shown on the vertical axis and the output voltage on the horizontal axis. Each calibration curve was obtained by increasing air pressure from zero to maximum and decreasing it back to zero in a step wise manner. The method of least squares was used to fit a straight line to the data. Based on that, the equation for the 95% confidential interval is: PM = -.854 + 7.735 V i 0.458 where, V is output voltage, and H; is the capillary pressure 52 53 o— _o>see:_ .3350 ”Ba ..._o> c motzo seize—o0 74 8%: - -.---. ....l- e ....... - I -. i i -- - WW \ i.\ - \\ - ...: \I. - -.-..ii: ...- I... 3:. .. ..-... IIIIWHK - cache: 0 ll... _ c—I c c— on co so on on on s: 081-! 'm3 54 head in cm of water. This interval is shown on Figure A-l. Figure A-l suggests that basic properties of the transducer remained constant over this two day period. The transducer was recalibrated for each.experiment.to account for small amounts of drift. 55 Part List: Aluminum cell was made at the Research Complex-Engineering Machine shop 5/8" x 1/4", 1 Bar High Flow Ceramic Plate (Part No. 604D02- B1M3 Soil Moisture Equipment Corp. Santa Barbara, CA.) Viton O-ring (National O-rings Company, Detroit Ball Bearing, Lansing, MI) 0.062" ID x 1/8" OD Teflon Tube (Upchurch Scientific Inc., Oak Harbor, WA) Variable Reluctance Pressure Transducer, Model No. CJVR (C.J. Enterprises Tarzana, CA) Carrier Demodulator Model No. CJCD—2061 (C.J. Enterprises Tarzana, CA) Bench Digital voltmeter (Part No. 8050A John Fluke MFG. Co. Plymouth, MI) 3-way Ball Valve Model No. ZZ-BZXJ-SSP (Parker Hannifin Corp., Instrumentation Valve Division, Jacksonville, AL) Air Valve (Three-way stopcock, Chemistry shop at MSU, E.Lansing, MI) Soltrol 170 Cat. No. AP1700 (Phillips 66 Company, Borger, TX) 25 ml. Burette with stop cock (Chemistry shop at MSU, E.Lansing, MI) 56 Experiments to determine the moisture profile at the end of drainage Experimental Run 1 2 3 4 5 6 7 Sample 1 40.7 36.1 40.4 49.4 39.9 48.5 39.0 Top Layer Sample 2 40.7 48.5 46.7 ' 47.2 43.0 48.5 41.3 Sample 3 48.4 55.0 37.5 50.1 44.3 53.5 34.8 Sample 1 47.4 42.8 55.3 43.5 45.7 56.2 47.3 Mid.Layer Sample 2 56.1 45.7 57.4 49.3 41.7 51.7 54.2 Sample 3 45.0 44.5 47.5 45.7 39.3 52.1 52.2 Sample 1 47.8 51.8 56.4 54.1 56.0 39.5 62.9 Bot.Layer Sample 2 46.5 57.4 57.2 50.4 65.9 44.3 57.0 Sample 3 44.8 51.6 59.2 46.9 69.4 49.0 52.3 57 PRESSURE TRANSDUCER VARIABLE RELUCTANCE--- MODEL CJVR RANGES OF 0.1 T0 500 PSIG 5 PSID ACCEPTS CORROSIVE LIQUIDS & GASES LOW VIBRATION & SHOCK SENSITIVITY HIGH NATURAL FREQUENCY 4 t! 4 DESCRIPTION The Model CJVR Variable Reluctance Pressure Transducer is designed to measure low and medium gage and differential pressures. In typical AC excited bridge circuits, the system provides a full scale output of approximately 25 millivolts per volt input at SKHz. The trans- ducer will operate with most carrier systems operating at a frequency between 3KHz and IOKHz. With C.J. carrier demodulators CJCD and most Pace carrier systems. the transducer will deliver a 0 to :SVDC or :lOVDC output. Constructed primarily of 400 series stainless steel. the transducer consists of basically of a flat pressure sensing dia- phragm (field replaceable) clamped between two matched case halves each containing electrical pickoff coils. Applied pressure deflects the diaphragm which is detected by the two pickoff coils. When the coils are connected as two opposing legs of a bridge circuit, the resultant bridge output is proportional to pressure. The pickoff coils are hermetically sealed in the case so as to isolate them from the pressure media. Bleed screws are provided in both case halves to facilitate complete liquid filling for dynamic measurements. SPECIFICATIONS ‘ RANGES: 0.1 to 500 psi gage & differential LINEARITY: :1/2% full scale (best fit straight line) HYSTERESIS: 1/2% full scale OVERPRESSURE: 2 times range with 1/2% F.S. maximum zero shift LINE PRESSURE: 25 times range or 500 psi, whichever is less OUTPUT: 25 mv/V nominal e SKHz INDUCTANCE: 10 mh/coil nominal @ SKHz, zero balance within 20% F-So PRESSURE MEDIA: Corrosive liquids & gases both sides compatible with 400 series stainless steel, Buna "N" and silver TEMPERATURE: Operational from -65° to +250°F. Compensated from 0° to +170°F. with nominal deviation from 70°F. calibration 0f 3% F.S. PRESSURE CAVITY: 4 x 10'3 cubic inches VOLUMETRIC 4 x 10‘4 cubic inches DISPLACEMENT: _ WEIGHT: 15 ounces .—.—-—— 14° . '——1.38—-" 36. PRESSURE III-27NPT _ ‘.J. ‘ {—— -/I-- ""I 1.20 I._._ /-¢- -£ / [’05. PRESSURE III-27"" / \.P08. BLED SCRDI NEG. ILnD SCREW ELECTRICAL COMR HR-C- 12$ . HATES HIT" HR-l-ZIC {—‘l"lf'['5J C. J. ENTERPRISES division of C. J. Instruments. Inc. P. 0. BOX 834 TARZANA, CA 91356 (818) 996-4131 58 CARRIER DEMODULATOR FOR VARIABLE RELUCTANCE TRANSDUCERS . MODELS CJCD-Rlll, CJCD-A 11M, AND CJCD-RlliD FEATURES “ llSVAC INPUT * UP TO ilOVDC OUTPUT * SMALL RUGGED CONSTRUCTION * OPERATES WITH C.J. 6 PACE TRANSDUCERS IDESCRIPTION The Model CJCD-élll Carrier Demodulator. designed for operation on unregulated IISVAC. 60Hz. operates with C.J. and Pace variable reluctance transducers to provide up to 0-10 or :IOVDC full scale output for voltage controlled telemetry and other DC systems. Ex- citation of 8 volts pk-pk at 4 KB: is applied to a bridge including the two inductance arms of the transducer. A solid-State amplifier and demodulator converts the bridge output to DC. Response time is less than 50 milliseconds. The assembly is packaged in a small lightweight aluminum housing with external digital turns-counting dials for zero and span control. Models CJCD-bllLM and CJCD-éllID are the same as the basic Model CJCD- bill except the CJCD-blllh incorporates a dial indicating readout and the CJCD—blllIJin- corporates a digital readout. SPECIFICATIONS POWER REQUIREMENTS: IISVAC. 60 Hz (specials available for DC operation) REGULATION: Better than 0.22 from a voltage level of 105 to IZSVAC at frequen- cies from 50 to 7082. OUTPUT: Full scale is adjustable from :IVDC to :10VDC into a 1000 ohm load or greater with a 10 turn digital turns counting dial. ZERO: Adjustable up to 3752 of full scale with a 10 turn digital turns counting dial. RESPONSE: Less than 50 milliseconds. ACCURACY: Better than 20.52 F.S. including linearity 6 drift. TEMPERATURE: 32°F. to I60'F. THERMAL EFFECT: 0.032 F.S./°F. maximum. WEIGHT: 24 ounces ourrur connecron wu-J-st "5°3‘31C reansoucra connecroa wx-c-izs """25 ua-c-st -—POHIR INPUT IISVAC wa-a-ztc T— 14 A / .--. ‘ ‘ 1 i. ' I "’ 1.: oureui:;:j : z cats-4:11 2 2 ' : 1 J | Ah J J ‘ ‘ , : ‘— 1 1 SVAC ELECTRICAL SCHWATIC 1::r \E:I A numuncsaLjU MODELS “€0-01!!! 6 CJCD-CIIID 2.” © O A a: g ::::: O 5.00 1_______ [5' - the C. J. ENTERPRISES division of C. J. Instruments, Inc. P. 0. BOX 8314 TARZANA, CA 91356 (818) 996-4131 I REFERENCES Bear J., 1979, Hydraulics of Ground Water, Mc.Graw Hill Inc., pp.190-224 Collins R.E., 1961, Flow of Fluids Through Porous Materials, Reinhols publishing Corp. New York Corey A.T., 1986, Mechanics of Immiscible Fluids in Porous Media, Water Resources Publications, pp.26—55 Corey A.T., Brooks R.H., 1975, Drainage Characteristic of Soils, Soil Science Society'of America Proceeding Vol. 39 Freeze R.A., Cherry J.A., 1979, Ground Water, Prentice Hall Inc., pp.18-45 Gardner W., Israelsen O.W., Edlefsen N.W. and Clyde H., The Capillary Potential Function and its Relation to Irrigation Practice, Physical Review, Second Series July-December, 1922, p. 196 Lenhard R.J. and Parker J.C., Measurement And Prediction of Saturation-Pressure Relationships in Three-Phase Porous Media System Richards L.A., The Usefulness of Capillary Potential to Soil Moisture and Plant Investigators, Journal of Agricultural Research, Vol. 37, No.1, 1928, pp.719-742 Su C., Brooks R.H., 1980, Water Retention Measurements for Soils, Journal of Irrigation and Drainage Division, ASCE, Vol. 106 No. IR2 Top G.C., Klute A. and Peters D.P., 1967, Comparison of Water Content-Pressure Head Data Obtained by Equilibrium, Steady State and Unsteady State Methods, Soil Science Society of America Proceeding Vol. 31 White N.F., Duke H.R., Sunada D.K., Corey A.T., 1972, Boundary Effects in the Desaturation of Porous Media, Soil Science Society of America Vol. 113 59 MICHIGAN STATE UNIV. 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