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Surface and Interface Chemistry  Rheology Valentim M. B. Nunes Engineering Unit of IPT 2014.

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Presentation on theme: "Surface and Interface Chemistry  Rheology Valentim M. B. Nunes Engineering Unit of IPT 2014."— Presentation transcript:

1 Surface and Interface Chemistry  Rheology Valentim M. B. Nunes Engineering Unit of IPT 2014

2 Rheology: Study of deformation and flow of matter The rheological studies allow to characterize colloid systems, namely colloidal dispersions and emulsions. The technological importance of rheology is manifest in areas such as rubbers, paints, textiles, pulp, etc. The rheological behavior depends on :  Viscosity of the dispersant phase  Concentration of particles  Particle size and shape  Molecular interactions Rheo = Deformation Logia = Science or Study

3 Importance of the rheological studies (examples) Production of paint: the paint should be easy to spread and do not seeping through the walls. Cosmetics and hygiene: how a cream spreads or the time it took to flow from a recipient. Stability of emulsions or suspensions.

4 Viscosity: the viscosity of a liquid measures the resistance offered to flow. A liquid is Newtonian when the tangential force per unit area between two parallel planes of fluid is proportional to the velocity gradient. Viscosity coefficient.

5 Methods of measurement Capillary method (Ostwald, Ubbelohde)

6 Rotational method (Couette viscometer) Particularly useful for non-Newtonian fluids.  - angular velocity of the outer cylinder.  - angular deflection of the inner cylinder.

7 Viscosity of dilute solutions and colloidal dispersions Concepts:

8 Spherical particles, hydrodynamic calculation: Einstein:  - volume fraction k =2.5 Solvation and asymmetry: the term  must also include the solvent which kinetically acts as part of the particles. The asymmetry of particles also has a great effect on viscosity.

9 Intrinsic viscosity The Intrinsic viscosity has inverse concentration units.

10 Determination of relative molecular weight of polymers from measurements of viscosity. Viscosity measurements cannot be used to distinguish between particles of different sizes but with the same format and degree of solvation. However, if the format (configuration) or solvation factor change with the size of the particle, then viscosity can be used to determine the size of the particles.

11 The intrinsic viscosity of a polymer solution is proportional to the molar mass. If the orientations of the macromolecular chain are random: Linear polymers in solution are more than oriented at random, and the relationship is (Mark and Houwink):  - depends on the configuration.

12 The following viscosities were measured for solutions of cellulose acetate in acetone, with concentration of 0.5 g/100 cm 3 : 10 -3 M r 85138204302  /10 -4 Pa.s 5.456.517.739.40 The viscosity of acetone at this temperature is 3.2×10 -4 Pa.s Derive an expression from these data that permits the routine determination of the relative molar mass of samples of cellulose acetate. What additional information from this expression? Shaw, Introduction to Colloid and Surface Chemistry, 4th ed., Butterworth- Heinemann, Oxford, 1991

13 log M r 4.935.145.315.48 log  i /c -0.85-0.69-0.55-0.41 The average configuration of polymers is between random and extended.

14 The viscosity of a range of solutions of polystyrene in toluene were measured at 25 °C: c/g.L -1 0246810  /10 -4 kg.m -1.s -1 5.586.156.747.357.988.64 Calculate the intrinsic viscosity and estimate the molar mass of polymer knowing that in the Mark-Houwink equation, k = 3.8×10 -5 L.g -1 and  = 0.63 Atkins, Physical Chemistry, Oxford University Press, Oxford, 2006

15 c/g.L -1 246810 100(  /  0 -1)/c 5.115.205.285.385.49

16 Newtonian and non-Newtonian behavior In some fluids, viscosity depends on the applied tension or the time of they application. For these fluids, viscosity is no more a constant for becoming a property dependent on the conditions under which the fluid is deformed or under tension. In this case, the viscosity of the fluid is called apparent viscosity Fluids NewtonianNon - Newtonian

17 Dilatant behavior: when the apparent viscosity increases with the application of a force (corn starch in water). Pseudo plastic behavior: when the apparent viscosity decreases with the application of a force (creams, ointments, etc.) tension viscosity Velocity gradient 1. Dilatant; 2. Newtonian; 3. Pseudo plastic Non- Newtonian behavior (independent of time)

18 Viscoplasticity or Bingham Fluids Fluids characterized by the existence of a value of tension that must be exceeded so that the material presents a viscous flow. It is necessary that the force exceeds this limit for seepage occurs (tomato sauce, etc.) tension Velocity gradient

19 Thixotropy and Antithixotropy (time- dependent) Certain materials present change of viscosity when the applied voltage is maintained for a certain time. Thixotropy: when the viscosity decreases with time of application of force and retrieves the initial state after prolonged rest (paints, oils, yogurt, etc.) Antithixotropy or Rheopexy: when the viscosity increases with time.

20 World’s Longest Running Laboratory Experiment – The Pitch Drop Experiment Pitch – derivative of tar. At room temperature feels solid and can be shattered with a blow of a hammer. This experiment shows that in fact at room temperature pitch is a fluid! http://www.physics.uq.edu.au/physics_museum/pitchdrop.shtml


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