KWAME NKRUMAH UNIVERSITY OF SCIENCE AND TECHNOLOGY COLLEGE OF ENGINEERING DEPARTMENT OF PETROLEUM ENGINEERING EXPERIMENT: SURFACE TENSION AND INTERFACIAL TENSION NAME: GAND OBED FIIFI FRANCIS INDEX NUMBER: 3521718 LAB SUPERVISOR: MR. MICHAEL OBBO GROUP NUMBER: THREE (3) DATE: 9TH MARCH, 2021 TABLE OF CONTENT TABLE OF CONTENT ............................................................................................................. 2 INTRODUCTION ..................................................................................................................... 4 AIM OF THE EXPIREMENT................................................................................................... 4 LITERATURE REVIEW .......................................................................................................... 4 MATERIALS AND APPARATUS ........................................................................................... 5 METHOD AND PROCEDURE ................................................................................................ 6 PRECAUTIONS ........................................................................................................................ 7 EXPERIMENTAL DATA AND OBSERVATION .................................................................. 8 OBSERVATIONS ..................................................................................................................... 8 CALCULATIONS ......................................................... Ошибка! Закладка не определена. DISCUSSIONS ........................................................................................................................ 12 EFFECTS OF TEMPERATURE ON SURFACE TENSION ................................................. 13 CONCLUSION ........................................................................................................................ 13 REFERENCES ........................................................................................................................ 13 FIGURE 1: ATTENSION SIGMA 700/701(TENSIOMETER) ............................................... 6 FIGURE 2: A GRAPH OF THE SURFACE TENSION OF TAP WATER AT ROOM TEMP. WITH RESPECT TO TIME ...................................................................................................... 9 FIGURE 3: A GRAPH OF THE SURFACE TENSION OF HEXANE AT ROOM TEMP. WITH RESPECT TO TIME ............................................................................................................... 10 FIGURE 4: A GRAPH OF THE INTERFACIAL TENSION OF HEXANE AND TAP WATER AT ROOM TEMP. WITH RESPECT TO TIME. ................................................................... 11 TABLE 1: EXPERIMENTAL DATA OF SURFACE TENSION OF TAP WATER WITH RESPECT TO TIME ................................................................................................................. 8 TABLE 2: EXPERIMENTAL DATA OF THE SURFACE TENSION OF HEXANE WITH RESPECT TO TIME ................................................................................................................. 9 TABLE 3: EXPERIMENTAL DATA OF THE INTERFACIAL TENSION OF HEXANE AND WATER WITH RESPECT TO TIME ..................................................................................... 10 INTRODUCTION AIM OF THE EXPIREMENT To determine the surface tension of tap water. To determine the surface tension of hexane. To determine the interfacial tension of hexane and tap water. To study the effects of temperature on surface tension (surface phenomenon). LITERATURE REVIEW The cohesive forces between liquid molecules are responsible for the phenomenon known as surface tension (ST). The molecules at the surface do not have the similar neighboring atoms on all sides and thus they cohere more strongly to those directly associated with them on the surface. This forms a surface “film” which makes it more difficult to move an object through the surface than move it when it is completely immersed. The same situation applies also at the interface of the two liquids that do not mix together. In this case the term interfacial tension (IFT) is used. If the surface area of the liquid is increased, more molecules are present at the surface, and work must be done for this to occur. Therefore, the surface has excess Gibbs energy relative to the interior of the liquid. There are several different units for surface and interfacial tension; typically, mN/m (which is equivalent to dynes/ cm) is used.1 One of the main factors affecting surface tension of pure liquids is the temperature. Experimentally it has been found that the surface tension decreases almost linearly with temperature. When temperature increases, the molecular thermal activity increases causing a decrease in cohesive interaction. This causes decrease in surface tension.2 Surface tension of pure liquids is also easily affected by certain impurities, called surfactants. Surfactants are amphiphilic molecules that include both hydrophobic (non-polar, water insoluble) and hydrophilic (polar, water soluble) segments. When surfactants are dissolved in water they orientated at the surface so that hydrophilic parts are in water and hydrophobic parts are in air. The surface tension is reduced as some of the water molecules are replaced by the surfactant molecules and interaction forces between surfactant and water is less than between two water molecules. The effectiveness of surfactant molecule is determined by the amount of surfactant needed and the minimum surface tension value that can be reached. This can be studied with critical micelle concentration (CMC) measurements as micelles are formed when the surfactant concentration is high enough to saturate the surface.2 The measurement of the surface and interfacial tension can be done by using Sigma force tensiometer. It is based on the force measurements of the interaction of a probe at the liquid-gas or liquid-liquid interface. A probe is hang on the balance and brought into contact with the liquid interface tested. The forces experienced by the balance as the probe interacts with the surface of the liquid can be used to calculate the surface tension. The forces present in this situation depend on the following factors; size and shape of the probe, contact angle between the probe and the liquid and surface tension of the liquid. The size and the shape of the probe are easily controlled. The probe is made of platinum which ensures the zero contact angle between the probe and the liquid to be studied. Two types of probes are commonly used; the Du Noüy ring and the Wilhelmy plate. A metal rod can also be used when the sample volume is limited.1 MATERIALS AND APPARATUS Hexane Tap water Sigma Tensiometer (One Attension software) Standard vessel Small vessel Du Noüy ring (probe) FIGURE 1: ATTENSION SIGMA 700/701(TENSIOMETER) METHOD AND PROCEDURE For the surface tension of tap water; The Du Noüy ring was placed on the hook in the measuring chamber. The measurement chamber was opened; the stage was lowered and the small vessel containing the tap water was placed on the stage after which it was raised again for the Du Noüy ring to hang just above the surface of the tap water. The measurement chamber was closed and the One Attension software was opened on a computer connected to the tensiometer. On the One Attension software, surface tension(ST)/interfacial tension(IFT) was selected, the probe selected was with ring, the experiment name was typed, the vessel used in the tensiometer which was the small vessel was selected and the phase was selected for the surface tension experiment. Finally, the program was ran to start the measurement of the surface tension of the tap water. For the surface tension of hexane; The Du Noüy ring was placed on the hook in the measuring chamber. The measurement chamber was opened; the stage was lowered and the small vessel containing the hexane was placed on the stage after which it was raised again for the Du Noüy ring to hang just above the surface of the hexane. The measurement chamber was closed and the One Attension software was opened on a computer connected to the tensiometer. On the One Attension software, surface tension(ST)/interfacial tension(IFT) was selected, the probe selected was with ring, the experiment name was typed, the vessel used in the tensiometer which was the small vessel was selected and the phase was selected for the surface tension experiment. Finally, the program was ran to start the measurement of the surface tension of the hexane. For the interfacial tension of water and hexane; With the Du Noüy ring already in place in the measurement chamber, the stage was lowered and the standard vessel containing hexane and tap water with hexane (light phase) settling on top was placed on the stage after which the stage was raised for the Du Noüy ring to touch the hexane-water contact of the mixture. The measurement chamber was closed and the One Attension software was opened on a computer connected to the tensiometer. On the One Attension software, surface tension(ST)/interfacial tension(IT) was selected, the probe selected was with ring, the experiment name was typed, the vessel used in the tensiometer which was the standard vessel was selected after which the phase was selected for the interfacial tension experiment of the hexane and tap water mixture. Finally, the program was ran to start the measurement of the interfacial tension of the hexane and water mixture. PRECAUTIONS The tensiometer was placed on a level and stable ground to avoid rupturing of the meniscus which will lead to the restart of the measurement which will intend prolong the experiment. The stage was lowered before placing any of the vessels on top. The measurement chamber was closed before the One Attension program was ran. For the measurement of the interfacial tension of the hexane and water mixture, the stage was raised so the Du Noüy ring will touch the hexane-water contact so as to measure interfacial tension and not surface tension of the hexane. EXPERIMENTAL DATA AND OBSERVATION OBSERVATIONS When the One Attension was ran and the ring was above the surface for the surface tension and in the hexane and water mixture, the force was zeroed. As the ring touched the surface for the surface tension experiment, there was a slight positive force due to the adhesive force between the ring and the surface. The ring was then pushed through the surface due to surface tension which caused a small increment force (the same thing also happened in the case of the interfacial tension). The ring broke the surface and there was a small positive force which was measured due to the supporting wires of the ring. When lifted through the surface, the measured force started to increase. The force kept increasing. The maximum force was reached. After the maximum, there was a small decrease of the force until the ring was pushed back below the surface.3 TABLE 1: EXPERIMENTAL DATA OF SURFACE TENSION OF TAP WATER WITH RESPECT TO TIME No. Time / sec ST / (mN/m) F/L (mN/m) F (mN) 1 63.387 69.091 73.754 8.879 2 83.238 68.778 73.443 8.841 3 104.238 68.743 73.408 8.837 4 124.529 68.723 73.389 8.835 5 144.888 68.662 73.328 8.828 6 165.698 68.622 73.328 8.828 7 186.927 68.636 73.302 8.825 8 207.375 68.610 73.276 8.821 9 227.966 68.499 73.166 8.808 10 248.464 68.523 73.190 8.811 A Graph of surface tension of tap water at room temperature. 69,2 Surface Tension (mN/M) 69,1 69 68,9 68,8 68,7 68,6 68,5 68,4 60 80 100 120 140 160 180 200 220 240 Time (s) FIGURE 2: A GRAPH OF THE SURFACE TENSION OF TAP WATER AT ROOM TEMP. WITH RESPECT TO TIME TABLE 2: EXPERIMENTAL DATA OF THE SURFACE TENSION OF HEXANE WITH RESPECT TO TIME No. Time / sec ST / (mN/m) F/L (mN/m) F (mN) 1 45.500 16.139 18.523 2.230 2 62.509 16.144 18.529 2.231 3 79.649 16.154 18.539 2.232 4 96.570 16.158 18.544 2.232 5 112.950 16.180 18.568 2.235 6 129.880 16.187 18.575 2.236 7 146.977 16.186 18.573 2.236 8 163.879 16.188 18.576 2.236 9 180.538 16.212 18.601 2.239 10 197.638 16.207 18.596 2.239 A Graph of surface tension of hexane at room temperature. 16,22 Surface Tension (mN/m) 16,21 16,2 16,19 16,18 16,17 16,16 16,15 16,14 16,13 40 60 80 100 120 140 160 180 200 Time (s) FIGURE 3: A GRAPH OF THE SURFACE TENSION OF HEXANE AT ROOM TEMP. WITH RESPECT TO TIME TABLE 3: EXPERIMENTAL DATA OF THE INTERFACIAL TENSION OF HEXANE AND WATER WITH RESPECT TO TIME No. Time / sec ST / (mN/m) F/L (mN/m) F (mN) 1 71.627 32.758 34.141 4.110 2 90.946 32.235 33.639 4.050 3 111.464 31.885 33.301 4.009 4 132.187 31.661 33.086 3.983 5 152.855 31.484 32.915 3.963 6 174.144 31.355 32.791 3.948 7 195.164 31.237 32.677 3.934 8 216.553 31.156 32.600 3.925 9 237.395 31.041 32.489 3.911 10 258.694 30.983 32.433 3.904 A Graph of interfacial tension of hexane and water at room temp. 33 32,8 Surface Tension (nM/m) 32,6 32,4 32,2 32 31,8 31,6 31,4 31,2 31 30,8 60 80 100 120 140 160 180 200 220 240 260 Time (s) FIGURE 4: A GRAPH OF THE INTERFACIAL TENSION OF HEXANE AND WATER AT ROOM TEMP. WITH RESPECT TO TIME. CALCULATION 𝐴𝑣𝑒𝑟𝑎𝑔𝑒 𝑜𝑓 𝑠𝑢𝑟𝑓𝑎𝑐𝑒 𝑡𝑒𝑛𝑠𝑖𝑜𝑛/𝑖𝑛𝑡𝑒𝑟𝑓𝑎𝑐𝑖𝑎𝑙 𝑡𝑒𝑛𝑠𝑖𝑜𝑛 = 𝑠𝑢𝑚 𝑜𝑓 𝑣𝑎𝑙𝑢𝑒𝑠 𝑛𝑢𝑚𝑏𝑒𝑟 𝑜𝑓 𝑣𝑎𝑙𝑢𝑒𝑠 For the average surface tension of tap water; 69.091 + 68.778 + 68.743 + 68.723 + 68.662 + 68.662 + 68.636 + 68.610 + 68.499 + 68.523 10 = 𝟔𝟖. 𝟔𝟗𝟑𝒎𝑵/𝒎 = For the average surface tension of hexane; 16.139 + 16.144 + 16.154 + 16.158 + 16.180 + 16.187 + 16.186 + 16.188 + 16.212 + 16.207 10 = 𝟏𝟔. 𝟏𝟕𝟔𝒎𝑵/𝒎 = For the average of the interfacial tension of hexane and water; 32.758 + 32.235 + 31.885 + 31.661 + 31.484 + 31.355 + 31.237 + 31.156 + 31.041 + 30.983 10 = 𝟑𝟏. 𝟓𝟖𝟎𝒎𝑵/𝒎 = DISCUSSIONS For the experiment of the surface tension of the tap water, it was seen that the surface tension decreased with time and this was as a result of the decrease in the cohesive force with time between the molecules of the tap water. Also, it can be observed that the surface tension of that of the hexane also decreased gradually with time and as said for that of the tap water, the forces within the molecules of the hexane decreased with time. For the experiment concerning the interfacial tension of the hexane and tap water, the same decrement in the values of the interfacial tension was seen and since force it directly proportional to the interfacial tension, it can be said that the decrement was also as a result of the decrease in the force. Now comparing the average surface tension of the tap water experiment to that of the liquid hexane (68.693 and 16.176 respectively), it can be noted the average surface tension of the tap water is higher than that of the hexane and this is because the affecting cohesive force and since surface tension is proportional to the force and there is a decrease in the force there will be a decrease in the surface tension as compared to that of tap water which has a strong cohesive force. Hence, obtaining an average surface tension of the tap water higher than that of the hexane. Surface tension observed between two liquids; water and hexane are known as the interfacial tension. This is defined to the interface of two immiscible liquids. The surface tension of water at room temperature was found to be 68.693 mN/m while that of liquid hexane; 16.176 mN/m. The interfacial tension which is “surface tension” between the two liquids was found to be 31.580 mN/m which is lower when compared to water but higher relative to liquid hexane. This is due to the fact that the polar to non-polar attraction between the unlike molecules yields an attractive force lower than the cohesive force in the polar liquid but higher than cohesive force in the non-polar liquid; hexane. EFFECTS OF TEMPERATURE ON SURFACE TENSION One of the main factors affecting surface tension of pure liquids is the temperature. Experimentally it has been found that the surface tension decreases almost linearly with temperature. When temperature increases, the molecular thermal activity increases causing a decrease in cohesive interaction. This causes decrease in surface tension.2 CONCLUSION Both surface tension and interfacial tension depend on the force of attraction between the molecules of the fluid(s); the stronger the force of attraction, the greater the value of either the surface tension or the interfacial tension and vice versa. Also, temperature has an effect on surface tension and it is inversely proportional. REFERENCES 1. Susanna Lauren, PHD, Biolin Scientific. Surface and Interfacial Tension and their Measurement Techniques. Attension [TN 2], page 1. 2. Susanna Lauren, PHD, Biolin Scientific. Surface and Interfacial Tension and their Measurement Techniques. Attension [TN 1], page 3. 3. Susanna Lauren, PHD, Biolin Scientific. Surface and Interfacial Tension and their Measurement Techniques. Attension [TN 2], page 2. 4. Gibbs. J. W. (2002) [1876-1878], “On the equilibrium of heterogeneous substances”, in Bumstead, H. A.; Van Nameeds, R. G., The Scientific Papers of J. Willard Gibbs, 1, Woodbridge, CT: Ox Bow Press, pp. 55-80, ISBN 091802477