Page 162 - Handbook Of Multiphase Flow Assurance
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158                        5.  Flow restrictions and blockages in operations








                 FIG. 5.30  Illustration of paraffin wax crystal with normal paraffin molecules organized together.

                   Molecules of various size crystallize as their crystallization temperature is reached. Largest
                 n-paraffins crystallize at higher temperatures, and usually determine the measurable param-
                 eter called the wax appearance temperature. The parameter is subjective and depends on the
                 laboratory's ability to detect the crystallization either by light, heat, force or pressure. Some
                 objectivity is added because modern laboratory equipment has relatively comparable sensi-
                 tivity levels.
                   There are several mechanisms for deposition of paraffins on walls of pipe or well tubing:
                 thermal and Brownian diffusion, and shear dispersion and settling. The most common one is
                 thermal diffusion. Paraffins will not deposit if temperature is above crystallization tempera-
                 ture. Paraffins will have almost no deposition on a pipe wall if there is no temperature differ-
                 ence between pipe wall and bulk oil because there is no driving force for paraffin molecules
                 to move toward the pipe wall. Normal paraffin molecules are usually driven from solution
                 in oil toward the pipe wall by the concentration difference in laminar flow and by turbulent
                 eddies in turbulent flow. When molecules reach the laminar sublayer, the diffusion mecha-
                 nism starts.
                   In turbulent flow there are three sublayers: concentration sublayer, thermal sublayer and
                 flow or momentum sublayer. Thermal sublayer should be used because it is at this bound-
                 ary where the transition to wax crystallization can occur. Concentration sublayer is slightly
                 smaller than thermal sublayer due to kinetic delay effects of wax crystallization.
                   The most illustrative description  of the three sublayers was shown by  Incropera et  al.
                 (2007). I update the illustration from that work here as shown in Fig. 5.31 to reflect the relative
                 thicknesses of the sublayers as described in Bird et al. (1960). Understanding the difference
                 between the three boundary layers is very important to the physical effects involved in wax
                 deposition.
                   Diffusion coefficient is assumed constant.



                                    Velocity
                                    Temperature

                                    Concentration
                                                        Velocity
                                                        boundary
                                                        layer
                                                             Temperature
                                                             boundary    Concentration
                                                             layer   boundary
                                                                    layer
                 FIG. 5.31  Illustration of boundary layers in flow of a mixture of hydrocarbons past a surface with component
                 precipitation.
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