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If a tube of very narrow bore (called capillary) is dipped in a liquid, it is found that the liquid in the capillary either ascends or descends relative to the surrounding liquid. This phenomenon is called capillarity. The root cause of capillarity is the difference in pressures on two sides of (concave and convex) curved surface of liquid. Examples of capillarity : (i) Ink rises in the fine pores of blotting paper leaving the paper dry. (ii) A towel soaks water. (iii) Oil rises in the long narrow spaces between the threads of a wick. (iv) Wood swells in rainy season due to rise of moisture from air in the pores. (v) Ploughing of fields is essential for preserving moisture in the soil. (vi) Sand is drier soil than clay. This is because holes between the sand particles are not so fine as compared to that of clay, to draw up water by capillary action.  

Angle of contact between a liquid and a solid is defined as the angle enclosed between the tangents to the liquid surface and the solid surface inside the liquid, both the tangents being drawn at the point of contact of the liquid with the solid.
\[\theta ={{90}^{o}}\] \[{{F}_{a}}>\frac{{{F}_{c}}}{\sqrt{2}}\] concave meniscus. Liquid wets the solid surface
\[\theta ={{90}^{o}}\] \[{{F}_{a}}=\frac{{{F}_{c}}}{\sqrt{2}}\] plane meniscus. Liquid does not wet the solid surface.
\[\theta >{{90}^{o}}\] \[{{F}_{a}}<\frac{{{F}_{c}}}{\sqrt{2}}\] convex meniscus. Liquid does not wet the solid surface.
(i) Its value lies between \[{{0}^{o}}\]and \[{{180}^{o}}\] \[\theta ={{0}^{o}}\] for pure water and glass,  \[\theta ={{8}^{o}}\] for tap water and glass, \[\theta ={{90}^{o}}\] for water and silver \[\theta ={{138}^{o}}\] for mercury and glass,  \[\theta ={{160}^{o}}\] for water and chromium (ii) It is particular for a given pair of liquid and solid. Thus the angle of contact changes with the pair of solid and liquid. (iii) It does not depends upon the inclination of the solid in the liquid. (iv) On increasing the temperature, angle of contact decreases. (v) Soluble impurities increases the angle of contact. (vi) Partially soluble impurities decreases the angle of contact.  

We know that a liquid assumes the shape of the vessel in which it is contained i.e. it can not oppose permanently any force that tries to change its shape. As the effect of force is zero in a direction perpendicular to it, the free surface of liquid at rest adjusts itself at right angles to the resultant force. When a capillary tube is dipped in a liquid, the liquid surface becomes curved near the point of contact. This curved surface is due to the resultant of two forces i.e. the force of cohesion and the force of adhesion. The curved surface of the liquid is called meniscus of the liquid. If liquid molecule A is in contact with solid (i.e. wall of capillary tube) then forces acting on molecule A are (i) Force of adhesion \[{{F}_{a}}\] (acts outwards at right angle to the wall of the tube). (ii) Force of cohesion \[{{F}_{c}}\] (acts at an angle \[{{45}^{o}}\] to the vertical). Resultant force \[{{F}_{N}}\] depends upon the value of \[{{F}_{a}}\] and \[{{F}_{c}}\]. If resultant force \[{{F}_{N}}\] make an angle \[\alpha \] with \[{{F}_{a}}\]. Then \[\tan \alpha =\frac{{{F}_{c}}\sin {{135}^{o}}}{{{F}_{a}}+{{F}_{c}}\cos {{135}^{o}}}=\frac{{{F}_{c}}}{\sqrt{2}\,{{F}_{a}}-{{F}_{c}}}\] By knowing the direction of resultant force we can find out the shape of meniscus because the free surface of the liquid adjust itself at right angle to this resultant force.  
If \[{{F}_{c}}=\sqrt{2}Fa\] \[\tan \alpha =\infty \]\[\therefore \]\[\alpha ={{90}^{o}}\] i.e. the resultant force acts vertically downwards. Hence the liquid meniscus must be horizontal. \[{{F}_{c}}<\sqrt{2}Fa\] \[\tan \alpha =\] positive  \[\therefore \]\[\alpha \] is acute angle i.e. the resultant force directed outside the liquid. Hence the liquid meniscus must be concave upward. \[{{F}_{c}}>\sqrt{2}Fa\] \[\tan \alpha =\] negative  \[\therefore \]\[\alpha \]  is obtuse angle i.e. the resultant force directed inside the liquid. Hence the liquid meniscus must be convex upward.
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Due to the property of surface tension a drop or bubble tends to contract and so compresses the matter enclosed. This in turn increases the internal pressure which prevents further contraction and equilibrium is achieved. So in equilibrium the pressure inside a bubble or drop is greater than outside and the difference of pressure between two sides of the liquid surface is called excess pressure. In case of a drop, excess pressure is provided by hydrostatic pressure of the liquid within the drop while in case of bubble the gauge pressure of the gas confined in the bubble provides it. Excess pressure in different cases is given in the following table :  
Plane surface Concave surface
\[\Delta P=0\] \[\Delta P=\frac{2T}{R}\]
Convex surface Drop
\[\Delta P=\frac{2T}{R}\] \[\Delta P=\frac{2T}{R}\]
Bubble in air Bubble in liquid
\[\Delta P=\frac{4T}{R}\] more...
If n small drops of radius r coalesce to form a big drop of radius R then surface area of the liquid decreases. Amount of surface energy released = Initial surface energy ? final surface energy                                         \[E=n4\pi {{r}^{2}}T-4\pi {{R}^{2}}T\]    
Various formulae of released energy  
\[4\pi T[n{{r}^{2}}-{{R}^{2}}]\] \[4\pi {{R}^{2}}T({{n}^{1/3}}-1)\] \[4\pi T{{r}^{2}}{{n}^{2/3}}({{n}^{1/3}}-1)\] \[4\pi T{{R}^{3}}\left[ \frac{1}{r}-\frac{1}{R} \right]\]      
(i) If this released energy is absorbed by a big drop, its temperature increases and rise in temperature can be given by \[\Delta \theta =\frac{3T}{JSd}\left[ \frac{1}{r}-\frac{1}{R} \right]\] (ii) If this released energy is converted into kinetic energy of a big drop without dissipation then by the law of conservation of energy. \[\frac{1}{2}m{{v}^{2}}=4\pi {{R}^{3}}T\left[ \frac{1}{r}-\frac{1}{R} \right]\]     \[\Rightarrow \] \[\frac{1}{2}\left[ \frac{4}{3}\pi {{R}^{3}}d \right]{{v}^{2}}=4\pi {{R}^{3}}T\left[ \frac{1}{r}-\frac{1}{R} \right]\]     \[\Rightarrow \] \[{{v}^{2}}=\frac{6T}{d}\left[ \frac{1}{r}-\frac{1}{R} \right]\]  \[\therefore \]  \[v=\sqrt{\frac{6T}{d}\left( \frac{1}{r}-\frac{1}{R} \right)}\]  

When a drop of radius R splits into n smaller drops, (each of radius r) then surface area of liquid increases. Hence the work is to be done against surface tension.   Since the volume of liquid remains constant therefore \[\frac{4}{3}\pi {{R}^{3}}=n\frac{4}{3}\pi {{r}^{3}}\]  \[\therefore \] \[{{R}^{3}}=n{{r}^{3}}\] Work done \[=T\times \Delta A=T\times \] [Total final surface area of \[n\] drops \[-\] surface area of big drop] \[=T[n4\pi {{r}^{2}}-4\pi {{R}^{2}}]\]  
Various formulae of work done  
\[4\pi T[n{{r}^{2}}-{{R}^{2}}]\] \[4\pi {{R}^{2}}T[{{n}^{1/3}}-1]\] \[4\pi T{{r}^{2}}{{n}^{2/3}}[{{n}^{1/3}}-1]\] \[4\pi T{{R}^{3}}\left[ \frac{1}{r}-\frac{1}{R} \right]\]      
If the work is not done by an external source then internal energy of liquid decreases, subsequently temperature decreases. This is the reason why spraying causes cooling. By conservation of energy, Loss in thermal energy = work done against surface tension \[JQ=W\] \[\Rightarrow \] \[JmS\Delta \theta =4\pi T{{R}^{3}}\left[ \frac{1}{r}-\frac{1}{R} \right]\] \[\Rightarrow \] \[\frac{4}{3}\pi {{R}^{3}}d\,S\Delta \theta =4\pi {{R}^{3}}T\left[ \frac{1}{r}-\frac{1}{R} \right]\]                        \[[\text{As}\,\,\,m\,=V\times d=\frac{4}{3}\pi \,{{R}^{3}}\times d]\] \[\therefore \] Decrease in temperature  \[\Delta \theta =\frac{3T}{JSd}\left[ \frac{1}{r}-\frac{1}{R} \right]\] where \[J=\] mechanical equivalent of heat, \[S=\] specific heat of liquid, \[d=\] density of liquid.  

(1) If the initial radius of liquid drop is \[{{r}_{1}}\] and final radius of liquid drop is \[{{r}_{2}}\] then \[W=T\times \]  Increment in surface area \[W=T\times 4\pi [r_{2}^{2}-r_{1}^{2}]\]                             [drop has only one free surface] (2) In case of soap bubble \[W=T\times 8\pi [r_{2}^{2}-r_{1}^{2}]\]                             [Bubble has two free surfaces]  

The molecules on the liquid surface experience net downward force. So to bring a molecule from the interior of the liquid to the free surface, some work is required to be done against the intermolecular force of attraction, which will be stored as potential energy of the molecule on the surface. The potential energy of surface molecules per unit area of the surface is called surface energy. Unit : \[Joule/{{m}^{2}}\] (S.I.) \[erg/c{{m}^{2}}\] (C.G.S.) Dimension : \[[M{{T}^{2}}]\] If a rectangular wire frame ABCD, equipped with a sliding wire LM dipped in soap solution, a film is formed over the frame. Due to the surface tension, the film will have a tendency to shrink and thereby, the sliding wire LM will be pulled in inward direction. However, the sliding wire can be held in this position under a force F, which is equal and opposite to the force acting on the sliding wire LM all along its length due to surface tension in the soap film. If T is the force due to surface tension per unit length, then \[F=T\times 2l\] Here l is length of the sliding wire \[LM\]. The length of the sliding wire has been taken as \[2l\] for the reason that the film has got two free surfaces. Suppose that the sliding wire LM is moved through a small distance x, so as to take the position \[L'M'\]. In this process, area of the film increases by \[2l\times x\] (on the two sides) and to do so, the work done is given by \[W=F\times x=(T\times 2l)\times x=T\times (2lx)=T\times \Delta A\] \[\therefore \] \[W=T\times \Delta A\] [\[\Delta A=\] Total increase in area of the film] If temperature of the film remains constant in this process, this work done is stored in the film as its surface energy. From the above expression \[T=\frac{W}{\Delta A}\] or \[T=W\] [If  \[\Delta A=1\]] i.e. surface tension may be defined as the amount of work done in increasing the area of the liquid surface by unity against the force of surface tension at constant temperature.

The maximum distance upto which the force of attraction between two molecules is appreciable is called molecular range \[(\approx {{10}^{-9}}m)\]. A sphere with a molecule as centre and radius equal to molecular range is called the sphere of influence. The liquid enclosed between free surface (PQ) of the liquid and an imaginary plane (RS) at a distance r (equal to molecular range) from the free surface of the liquid form a liquid film. To understand the concept of tension acting on the free surface of a liquid, let us consider four liquid molecules like A, B, C and D. Their sphere of influence are shown in the figure. (1) Molecule A is well within the liquid, so it is attracted equally in all directions. Hence the net force on this molecule is zero and it moves freely inside the liquid. (2) Molecule B is little below the free surface of the liquid and it is also attracted equally in all directions. Hence the resultant force acts on it is also zero. (3) Molecule C is just below the upper surface of the liquid film and the part of its sphere of influence is outside the free liquid surface. So the number of molecules in the upper half (attracting the molecules upward) is less than the number of molecule in the lower half (attracting the molecule downward). Thus the molecule C experiences a net downward force. (4) Molecule D is just on the free surface of the liquid. The upper half of the sphere of influence has no liquid molecule. Hence the molecule D experiences a maximum downward force. Thus all molecules lying on surface film experiences a net downward force. Therefore, free surface of the liquid behaves like a stretched membrane.  

(1) The oil and grease spots on clothes cannot be removed by pure water. On the other hand, when detergents (like soap) are added in water, the surface tension of water decreases. As a result of this, wetting power of soap solution increases. Also the force of adhesion between soap solution and oil or grease on the clothes increases. Thus, oil, grease and dirt particles get mixed with soap solution easily. Hence clothes are washed easily. (2) The antiseptics have very low value of surface tension. The low value of surface tension prevents the formation of drops that may otherwise block the entrance to skin or a wound. Due to low surface tension, the antiseptics spreads properly over wound. (3) Surface tension of all lubricating oils and paints is kept low so that they spread over a large area. (4) Oil spreads over the surface of water because the surface tension of oil is less than the surface tension of cold water. (5) A rough sea can be calmed by pouring oil on its surface. (6) In soldering, addition of ?flux? reduces the surface tension of molten tin, hence, it spreads.  


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