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Minimum gas speed in heat exchangers to avoid particulate fouling

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3946 M.S. Abd-Elhady et al. / International Journal of Heat and Mass Transfer 47 (2004) 3943–3955Fig. 2. Particle size distributions (PSD, left) and scann<strong>in</strong>g electron microscope (SEM, right) pho<strong>to</strong>s of glass (a,b), bronze (c,d) andcopper particles (e,f), respectively.The cool<strong>in</strong>g airflow rate is also controlled through acritical nozzle and a pressure regula<strong>to</strong>r.Foul<strong>in</strong>g of the <strong>heat</strong> exchanger tube is moni<strong>to</strong>redus<strong>in</strong>g a digital camera through a glass w<strong>in</strong>dow <strong>in</strong>stalled<strong>in</strong> the <strong>heat</strong> exchanger section as shown <strong>in</strong> Fig. 1b. Thedigital camera is the F<strong>in</strong>epix S602 zoom, with a resolutionof 2832 pixels · 2128 pixels, i.e. 6.03 million pixels.The digital camera has a 6· optical zoom which compared<strong>to</strong> small image format has a zoom area of 35–210mm. The foul<strong>in</strong>g layer thickness is measured optically.Images are taken of the <strong>heat</strong> exchanger tubes before anddur<strong>in</strong>g foul<strong>in</strong>g. The clean <strong>heat</strong> exchanger tube radius istaken as a reference. The tube radii <strong>in</strong> the camera imagesand hence the foul<strong>in</strong>g layer thicknesses are determ<strong>in</strong>edwith an accuracy of ±1 pixel which corresponds <strong>to</strong> ±0.04mm. The temperatures of the hot air and the cool<strong>in</strong>g airbefore and after the <strong>heat</strong> exchanger are measured us<strong>in</strong>gK type thermocouples with an accuracy of ±0.4 °C. Theair <strong>speed</strong> at the exit of the <strong>heat</strong> exchanger section ismeasured by a hot wire anemometer with an accuracy of±0.015 m/s. Air exhaust from the setup is filteredthrough a bag filter before it goes <strong>in</strong><strong>to</strong> the atmosphere.Each foul<strong>in</strong>g experiment is carried out <strong>in</strong> the follow<strong>in</strong>gprocedure: Hot and cold airflow rates are adjusted<strong>to</strong> the desired flow rates at the beg<strong>in</strong>n<strong>in</strong>g of theexperiment. The hot air temperature is adjusted throughthe air <strong>heat</strong>er and the experiment is kept runn<strong>in</strong>g till asteady state is reached. After a steady state has beenreached, particles are <strong>in</strong>jected at the desired rate and thefoul<strong>in</strong>g process is moni<strong>to</strong>red.3. Results and discussion3.1. Influence of flow <strong>speed</strong> on growth of foul<strong>in</strong>g layerThe follow<strong>in</strong>g experiments are performed <strong>to</strong> see the<strong>in</strong>fluence of flow <strong>speed</strong> on the growth of the foul<strong>in</strong>g layerand <strong>to</strong> determ<strong>in</strong>e the flow <strong>speed</strong> at which foul<strong>in</strong>g ceases.Two types of particles are used <strong>in</strong> the experiments, thenon-metallic glass particles and the metallic bronze andcopper particles def<strong>in</strong>ed <strong>in</strong> the previous section.In the first experiments, glass particles have been<strong>in</strong>jected <strong>in</strong> the flow at different <strong>gas</strong> flow <strong>speed</strong>s and thefoul<strong>in</strong>g behavior is moni<strong>to</strong>red. The average airflow<strong>speed</strong> between the tubes has been changed from 2.7 <strong>to</strong>3.8 <strong>to</strong> 5 m/s and <strong>in</strong> each case the operat<strong>in</strong>g time was 9 h.The air temperature is 200 °C and the particles


M.S. Abd-Elhady et al. / International Journal of Heat and Mass Transfer 47 (2004) 3943–3955 3947Fig. 3. Foul<strong>in</strong>g layer at the end of 9 h of operation for different flow <strong>speed</strong>s. The foulant is spherical glass particles of diameter 21 ± 16lm. (a) V ¼ 2:7 m/s; (b) V ¼ 3:8 m/s; (c) V ¼ 5 m/s.Table 1Comparison between the foul<strong>in</strong>g behaviors for glass particles under different operat<strong>in</strong>g conditionsAverage airflow <strong>speed</strong> between the HE V ¼ 2:7 m/s V ¼ 3:8 m/s V ¼ 5 m/stubesF<strong>in</strong>al thickness (mm) 1 0.75 0.3Circumferential and radial growth Cont<strong>in</strong>ues Starts very fast and thendecreases abruptlyStarts very fast and thendecreases abruptlyconcentration is 0.15 g/N m 3 of flow<strong>in</strong>g air. Fig. 3 showsthe foul<strong>in</strong>g layer at the end of operation for the abovementionedcases. Table 1 shows a comparison betweenthe three different cases. It is shown that as the <strong>speed</strong> ofthe flow <strong>in</strong>creases, the foul<strong>in</strong>g layer surface area andthickness are reduced. Increas<strong>in</strong>g the average air <strong>speed</strong>between the <strong>heat</strong> exchanger (HE) tubes from 2.7 <strong>to</strong> 5 m/sreduces the f<strong>in</strong>al foul<strong>in</strong>g layer thickness from 1 <strong>to</strong> 0.3mm after 9 h of operation. When the average flow <strong>speed</strong>between the HE tubes is 2.7 m/s, it is found that thecircumferential and radial growth of the foul<strong>in</strong>g layercont<strong>in</strong>ued from the beg<strong>in</strong>n<strong>in</strong>g till the end of the experiment.Increas<strong>in</strong>g the average flow <strong>speed</strong> between the HEtubes <strong>to</strong> 3.8 and 5 m/s showed a different foul<strong>in</strong>gbehavior. The foul<strong>in</strong>g rate was very high at the beg<strong>in</strong>n<strong>in</strong>g,especially for the first 3 h. Then the foul<strong>in</strong>g ratestarted <strong>to</strong> decrease abruptly for the next 6 h of operation,till hardly any radial or circumferential growth canbe seen.Figs. 4 and 5 show the growth of the foul<strong>in</strong>g layer forglass particles over the <strong>heat</strong> exchanger tube as a functionof time. The average air <strong>speed</strong> between the tubes is 2.7m/s for Fig. 4 and 3.8 m/s for Fig. 5. Fig. 4a shows thatat the beg<strong>in</strong>n<strong>in</strong>g of the foul<strong>in</strong>g process, some particlesstart <strong>to</strong> deposit at <strong>in</strong>termittent and distant positions.These po<strong>in</strong>ts of deposition start <strong>to</strong> grow radially, Fig.4b–e, till the whole surface of the <strong>heat</strong> exchanger tube iscovered completely with particles, Fig. 4f. The surficialgrowth of the foul<strong>in</strong>g layer is emphasized by the encircledareas <strong>in</strong> Figs. 4a–f. The surficial growth of thefoul<strong>in</strong>g layer can be expla<strong>in</strong>ed by the fact that f<strong>in</strong>eparticles are most likely <strong>to</strong> stick first <strong>to</strong> the HE tubesbecause of their higher stick<strong>in</strong>g velocity compared <strong>to</strong>coarse particles [7]. Then larger particles, which deposi<strong>to</strong>n the <strong>heat</strong> exchanger tube and stand alone <strong>in</strong> theshear<strong>in</strong>g flow, start <strong>to</strong> roll over the <strong>heat</strong> exchanger tubeif the shear<strong>in</strong>g flow <strong>speed</strong> is above a certa<strong>in</strong> limit. Theparticle roll<strong>in</strong>g motion is s<strong>to</strong>pped when it is blocked by astand<strong>in</strong>g heap of particles, which leads <strong>to</strong> the surficialgrowth of the fouled areas till they cover the unfouledsurfaces. The flow <strong>speed</strong> required <strong>to</strong> roll a particlerest<strong>in</strong>g on a flat surface, and, the stick<strong>in</strong>g velocity of aparticle, will respectively be discussed <strong>in</strong> detail <strong>in</strong> thefollow<strong>in</strong>g subsequent sections.Fig. 5 shows that at the beg<strong>in</strong>n<strong>in</strong>g of the foul<strong>in</strong>gexperiment, Fig. 5b, the glass particles <strong>in</strong> the flow started<strong>to</strong> deposit on the rear end of the HE tube and cont<strong>in</strong>ued<strong>to</strong> the circumference, Fig. 5c–e. The rear end of the <strong>heat</strong>exchanger, Fig. 5f, is subjected <strong>to</strong> the lowest shear<strong>in</strong>gforces due <strong>to</strong> separation of flow from the tube surface,Achenbach [9]. The flow field for the exam<strong>in</strong>ed HEshown <strong>in</strong> Fig. 1 is solved us<strong>in</strong>g the f<strong>in</strong>ite volume methodapplied by the commercial CFD-package CFX version4.2. The low Reynolds number k–e model is used <strong>to</strong> solvethe flow field around the HE tubes. For all but theadvection terms, use is made of a second-order centraldifferenc<strong>in</strong>g scheme. In the equations for the velocitycomponents, use is made of the third order QUICK<strong>in</strong>terpolation scheme for the advection terms. For the kand e equations the first order HYDRID-scheme is appliedwhich is more stable than the QUICK scheme andensures the k and e values <strong>to</strong> rema<strong>in</strong> positive <strong>in</strong> theconverged solution. In the computations use is made ofthe SIMPLEC pressure-correction scheme <strong>in</strong> which thepressure field is <strong>in</strong>directly specified via the cont<strong>in</strong>uityequation. For the u and the v velocity use is made of theS<strong>to</strong>ne’s method, for the turbulence quantities a l<strong>in</strong>erelaxationmethod is used and an algebraic multi-gridmethod is applied for the pressure equation. The flowfield is solved for a turbulent flow, at Re ¼ 2 10 5 , which


3948 M.S. Abd-Elhady et al. / International Journal of Heat and Mass Transfer 47 (2004) 3943–3955Fig. 4. Progress of the foul<strong>in</strong>g layer over the HE tube with<strong>in</strong> 9 h of operation. The foulant is spherical glass particles of diameter21 ± 16 lm. The average air <strong>speed</strong> between the HE tubes is 2.7 m/s: (a) after 1 h of operation, (b) after 1.5 h of operation, (c) after 2 h ofoperation, (d) after 2.5 h of operation, (e) after 3 h of operation, (f) after 9 h of operation.Fig. 5. Growth of the foul<strong>in</strong>g layer over the HE tube with<strong>in</strong> 6 h of operation. The foulant is spherical glass particles of diameter 21 ± 16lm. The average air <strong>speed</strong> between the tubes is 3.8 m/s: (a) at the beg<strong>in</strong>n<strong>in</strong>g, (b) after 0.5 h of operation, (c) after 1 h of operation, (d)after 1.5 h of operation, (e) after 2 h of operation, (f) after 6 h of operation.corresponds <strong>to</strong> a superficial flow velocity of 10 m/s. Fig. 7shows the velocity con<strong>to</strong>urs <strong>in</strong> the y and x directions forthe HE shown <strong>in</strong> Fig. 1. Although the CFD calculationsshow that the flow around the middle centered tube is notperiodic, this centered tube can be regarded as a representativefor a tube <strong>in</strong> a tube bundle. It is shown that for


M.S. Abd-Elhady et al. / International Journal of Heat and Mass Transfer 47 (2004) 3943–3955 3949Fig. 6. A summary for the foul<strong>in</strong>g layer circumferential growth shown <strong>in</strong> Fig. 5.the middle centered tube the flow keeps attached <strong>to</strong> thetube surface and then separates at an angle of 120° fromthe stagnation po<strong>in</strong>t. From the numerical results it couldalso be concluded that there is more air circulation at thefront than <strong>in</strong> the rear end of the middle centered HEtube, Fig. 7c and d. Therefore particles that stick <strong>to</strong> therear end of the HE tube are more likely <strong>to</strong> rema<strong>in</strong> <strong>in</strong>position than particles that stick <strong>to</strong> the sides of the HEtube. A particle that sticks <strong>to</strong> the side of the HE tube rollsover the HE tube if the airflow <strong>speed</strong> is above a certa<strong>in</strong>limit, and s<strong>to</strong>ps if it is blocked by the rest<strong>in</strong>g particles atthe rear end of the <strong>heat</strong> exchanger tube. Therefore foul<strong>in</strong>gstarts at areas that are subjected <strong>to</strong> m<strong>in</strong>imum shear<strong>in</strong>gforces and then spreads due <strong>to</strong> particle transport <strong>to</strong>the already deposited particles. Fig. 6 summarizes thecircumferential growth of the foul<strong>in</strong>g layer shown <strong>in</strong> Fig.5.3.2. Limit<strong>in</strong>g foul<strong>in</strong>g <strong>speed</strong>The previous set of experiments has shown that asthe flow <strong>speed</strong> <strong>in</strong> the HE <strong>in</strong>creases, the thickness and thesurface area of the foul<strong>in</strong>g layer deposited over the HEtube are reduced. The follow<strong>in</strong>g experiments are done <strong>to</strong>determ<strong>in</strong>e the flow <strong>speed</strong> at which foul<strong>in</strong>g of the <strong>heat</strong>exchanger is prevented. The results of the experimentwill be compared <strong>to</strong> the results achieved with an analyticalmodel. The analytical model is only valid forspherical non-charged particles. The analytical model isbased on the m<strong>in</strong>imum shear velocity required <strong>to</strong> roll aparticle on a flat surface. It can be applied for a cyl<strong>in</strong>dricaltube if the particle diameter is much smaller thanthe cyl<strong>in</strong>der diameter, as is the case here. The shear flow<strong>speed</strong> required <strong>to</strong> roll a particle deposited on a flatsurface is called the critical flow velocity and it is afunction of the particle material and size and the surfacematerial. The critical flow velocity can be calculatedwhen assum<strong>in</strong>g that the hydrodynamic roll<strong>in</strong>g momentdue <strong>to</strong> the drag force, F d , lift force, F L , and buoyancyforce, F b , is greater than the rest<strong>in</strong>g adhesion momentdue <strong>to</strong> the surface adhesion force, F a , and the force ofgravity, F g . The ratio between the hydrodynamic roll<strong>in</strong>gmoment and the adhesion rest<strong>in</strong>g moment is def<strong>in</strong>ed byZhang et al. [10] as RM and equal <strong>to</strong>RM ¼¼Hydrodynamic roll<strong>in</strong>g momentAdhesion rest<strong>in</strong>g momentF d ð1:399R aÞðF a þ F g F b F L Þd=2 ; ð1Þwhere R, d and a are the particle radius, contact diameterand the particle radius of deformation, respectively.If the RM value is greater than 1, roll<strong>in</strong>g will takeplace. Abd-Elhady et al. [5] have calculated the criticalflow velocity for spherical copper particles of diametersrang<strong>in</strong>g from 5 <strong>to</strong> 50 lm, the results are shown <strong>in</strong> Fig. 8.The ma<strong>in</strong> flow stream velocity, i.e. the critical flowvelocity, required <strong>to</strong> roll a copper particle of 10 lm is10.5 m/s while for a 50 lm copper particle this velocity is4.5 m/s.Due <strong>to</strong> the comparison with the analytical modelpresented above, <strong>in</strong> the experiments only sphericalmetallic particles are used. The HE is operated at differentair flow<strong>in</strong>g <strong>speed</strong>s and different particle sizes <strong>to</strong>determ<strong>in</strong>e the operat<strong>in</strong>g <strong>speed</strong> at which foul<strong>in</strong>g is preventedas function of the particles size <strong>in</strong> the flow. Theflow <strong>speed</strong> at which foul<strong>in</strong>g is prevented, is <strong>in</strong>vestigatedfor copper particles of average diameter 10 lm with astandard deviation of 5 lm suspended <strong>in</strong> the airflow andalso for bronze particles of average diameter 55 lm witha standard deviation of 6 lm. The air temperature is 20°C and the particle concentration is 2 g/m 3 of airflow.The <strong>heat</strong> exchanger is kept runn<strong>in</strong>g for 8 h <strong>in</strong> eachexperiment. Experimental results of the foul<strong>in</strong>g experimentare plotted <strong>in</strong> Fig. 8. Fig. 8 shows that when air iscontam<strong>in</strong>ated with the copper particles of averagediameter 10 lm the HE tubes fouled when the averageflow <strong>speed</strong> between the tubes was lower than 9.5 m/s, i.e.


3950 M.S. Abd-Elhady et al. / International Journal of Heat and Mass Transfer 47 (2004) 3943–3955Fig. 7. Velocity con<strong>to</strong>urs <strong>in</strong> the y (left) and x (right) directions for the HE section (a,b) shown <strong>in</strong> Fig. 1b and for the middle centeredtube (c,d), respectively. Reynolds number is 2 · 10 5 .7.5 and 2.7 m/s. It is also shown that when the air iscontam<strong>in</strong>ated with the bronze particles of averagediameter 55 lm the HE tubes fouled when the averageflow <strong>speed</strong> between the tubes was lower than 5.5 m/s, i.e.4.5 and 2 m/s. Fig. 9 shows images for the HE tube at theend of the foul<strong>in</strong>g experiments <strong>in</strong> case the airflow iscontam<strong>in</strong>ated with bronze particles of average diameter55 lm. Fig. 9 shows that when the flow <strong>speed</strong> betweenthe tubes is equal <strong>to</strong> 2 m/s the foul<strong>in</strong>g layer thicknessbecomes 0.3 mm and dim<strong>in</strong>ishes when the flow <strong>speed</strong>becomes 5.5 m/s. The m<strong>in</strong>imum flow <strong>speed</strong> at whichfoul<strong>in</strong>g <strong>in</strong> a <strong>heat</strong> exchanger is prevented will be called thelimit<strong>in</strong>g foul<strong>in</strong>g <strong>speed</strong>.The copper particles used <strong>in</strong> the experiments have awide particle size distribution rang<strong>in</strong>g from 1 <strong>to</strong> 20 lm,as shown <strong>in</strong> Fig. 2e. Surpris<strong>in</strong>gly, no foul<strong>in</strong>g was found


M.S. Abd-Elhady et al. / International Journal of Heat and Mass Transfer 47 (2004) 3943–3955 3951Air flow velocity (m/s) .1614121086420Copper particles0 10 20 30 40 50 60Particle's diameter (µm).of the copper particles smaller than 10 lm at a flowvelocity of 9.5 m/s. This could be due <strong>to</strong> the smallamount of the f<strong>in</strong>e particles present and due <strong>to</strong> the removalof them by larger hitt<strong>in</strong>g particles. The removal off<strong>in</strong>e particles by the large deposit<strong>in</strong>g particles leads <strong>to</strong> alower limit<strong>in</strong>g foul<strong>in</strong>g <strong>speed</strong> than the limit<strong>in</strong>g foul<strong>in</strong>g<strong>speed</strong>, which corresponds <strong>to</strong> the smallest particle <strong>in</strong> the<strong>gas</strong> flow. The effect of the particle size distribution onthe foul<strong>in</strong>g mechanism still has <strong>to</strong> be <strong>in</strong>vestigated.The critical flow velocity shown <strong>in</strong> Fig. 8 is calculatedfor a metallic non-charged spherical copper particlerest<strong>in</strong>g on a good conduc<strong>to</strong>r surface. In case of anelectrically charged particle rest<strong>in</strong>g on a bad conduc<strong>to</strong>rsurface like glass an electrostatic adhesion force isdeveloped which leads <strong>to</strong> a higher critical flow velocitythan <strong>in</strong> case of a non-charged particle. The critical flowvelocity then should be calculated based on the nature ofthe particles <strong>in</strong> the flow and the flow conditions.3.3. Stick<strong>in</strong>g of particlesCritical flow velocity (Theoretical).No Foul<strong>in</strong>g Condition (Experimental).Foul<strong>in</strong>g Condition (Experimental).Bronze particlesFig. 8. The critical flow velocity and limit<strong>in</strong>g foul<strong>in</strong>g <strong>speed</strong>versus particle diameter.In practical applications of <strong>heat</strong> <strong>exchangers</strong> especially<strong>in</strong> waste <strong>in</strong>c<strong>in</strong>era<strong>to</strong>rs, the flue <strong>gas</strong>es conta<strong>in</strong> a wide rangeof particle sizes. To prevent foul<strong>in</strong>g of <strong>heat</strong> <strong>exchangers</strong>based on the critical flow velocity, the critical flowvelocity should be selected based on the particle sizemost likely <strong>to</strong> stick first <strong>to</strong> the <strong>heat</strong> exchanger tubes. Thefollow<strong>in</strong>g experiments have been done <strong>to</strong> determ<strong>in</strong>ewhich particle size deposits first from a batch of particlesflow<strong>in</strong>g over a <strong>heat</strong> exchanger tube. A mixture of equalmasses of bronze and copper particles is <strong>in</strong>jected <strong>in</strong><strong>to</strong> theairflow. The bronze and copper particles used are def<strong>in</strong>ed<strong>in</strong> the experimental setup section. The particlesconcentration is 2 g/m 3 of airflow. Hot air at 200 °C andflow rate of 13E)3 Nm 3 /s is passed <strong>to</strong> the <strong>heat</strong> <strong>exchangers</strong>ection. This results <strong>in</strong> a Reynolds number of700 based on the HE tube diameter and the superficialflow velocity. An airflow rate of 1.5E)3 Nm 3 /s and atemperature of 20 °C was used for cool<strong>in</strong>g the <strong>heat</strong> exchangertube <strong>in</strong>ternally. The <strong>heat</strong> exchanger has run for9 h. At the end of the foul<strong>in</strong>g experiment samples aretaken from the foul<strong>in</strong>g layer deposited on the <strong>heat</strong> exchangertube and these are exam<strong>in</strong>ed by SEM. Twosamples of particles are taken from the foul<strong>in</strong>g layerdeposited on the middle centered tube of the <strong>heat</strong> <strong>exchangers</strong>ection: The first sample of particles was scratchedfrom the <strong>to</strong>p of the foul<strong>in</strong>g layer. The secondsample of particles was scratched from the first foul<strong>in</strong>glayer of particles, which had deposited on the tube of the<strong>heat</strong> exchanger. This sample was taken by blow<strong>in</strong>g airthrough the HE at a very high <strong>speed</strong> such that most ofthe foul<strong>in</strong>g layer was blown off and only a very th<strong>in</strong> layerof particles rema<strong>in</strong>ed on the tube of the <strong>heat</strong> exchanger.Fig. 10 shows SEM pictures for the particles at thebot<strong>to</strong>m (near the <strong>heat</strong> exchanger tube) and at the <strong>to</strong>p ofthe foul<strong>in</strong>g layer respectively. First the f<strong>in</strong>e copper particleshave accumulated over the <strong>heat</strong> exchanger tubeand then afterwards the larger bronze particles. The <strong>to</strong>pof the foul<strong>in</strong>g layer consisted ma<strong>in</strong>ly of the large bronzeparticles surrounded by the f<strong>in</strong>e copper particles.The same k<strong>in</strong>d of experiment above is repeated us<strong>in</strong>gspherical glass particles <strong>in</strong>stead of us<strong>in</strong>g a mixture ofFig. 9. Pho<strong>to</strong>s for the exam<strong>in</strong>ed <strong>heat</strong> exchanger tube at the end of operation under different airflow velocities: (a) V ¼ 2 m/s, a bronzelayer of thickness 0.3 mm is formed on the HE steel tube; (b) V ¼ 4:5 m/s, a very f<strong>in</strong>e layer of bronze particles is formed; (c) V ¼ 5:5 m/s, no foul<strong>in</strong>g.


3952 M.S. Abd-Elhady et al. / International Journal of Heat and Mass Transfer 47 (2004) 3943–3955Fig. 10. Scann<strong>in</strong>g electron microscope pho<strong>to</strong>s for the particles at the bot<strong>to</strong>m (left) and <strong>to</strong>p (right) of the foul<strong>in</strong>g layer. The foul<strong>in</strong>g layeris composed of a mixture of copper and bronze particles.Fig. 11. Scann<strong>in</strong>g electron microscope pho<strong>to</strong>s for the particles at the bot<strong>to</strong>m (left) and <strong>to</strong>p (right) of the foul<strong>in</strong>g layer. The particles aremade of glass.bronze and copper particles. Fig. 11 shows SEM pho<strong>to</strong>sfor the particles at the bot<strong>to</strong>m (near the <strong>heat</strong> exchangertube) and <strong>to</strong>p of the foul<strong>in</strong>g layer. At the <strong>to</strong>p of thefoul<strong>in</strong>g layer large particles have accumulated with smallparticles <strong>in</strong> between. In the foul<strong>in</strong>g layer near the tube ofthe <strong>heat</strong> exchanger, the f<strong>in</strong>est particles <strong>in</strong> the flow haveagglomerated <strong>to</strong>gether <strong>to</strong> form islands of f<strong>in</strong>e particlesconnected <strong>to</strong> bigger particles. Fig. 12 and Table 2 show acomparison between the particles size distribution of the<strong>in</strong>jected glass particles <strong>in</strong> the airflow and the glass particles<strong>in</strong> the foul<strong>in</strong>g layer near the HE tube. It is shownthat the average diameter of the glass particles has reducedfrom 20.4 lm <strong>in</strong> the airflow <strong>to</strong> 14.7 lm <strong>in</strong>thefoul<strong>in</strong>g layer near the HE tube. 90% of the <strong>in</strong>jected glassparticles <strong>in</strong> the airflow have a diameter less than 43.1 lmwhile 90% of the glass particles <strong>in</strong> the foul<strong>in</strong>g layer nearthe HE tube have a diameter less than 25.2 lm. Thereduction <strong>in</strong> particle size <strong>in</strong> the foul<strong>in</strong>g layer near the HEtube from the particle size <strong>in</strong> the airflow is due <strong>to</strong> thehigher stick<strong>in</strong>g velocity of small particles compared <strong>to</strong>large particles as def<strong>in</strong>ed by Rogers and Reed [7].Rogers and Reed [7] developed a model that describesthe adhesion of a particle <strong>to</strong> a surface follow<strong>in</strong>g anelastic–plastic impact. The model is based upon considerationof the energy balance dur<strong>in</strong>g a normal impactbetween a sphere and a massive plane. The model describesthe adhesion of a particle aris<strong>in</strong>g from only elasticdeformations occurr<strong>in</strong>g dur<strong>in</strong>g the approach of the particle<strong>to</strong> the surface. When the particle velocity is reduced<strong>to</strong> zero dur<strong>in</strong>g the approach phase, part of the particle<strong>in</strong>itial k<strong>in</strong>etic energy, Q k , is converted <strong>in</strong><strong>to</strong> s<strong>to</strong>red elasticenergy, Q E , while the rema<strong>in</strong>der, Q L , is dissipated. This isthen followed by the recovery of the s<strong>to</strong>red elastic energy,which is converted <strong>in</strong><strong>to</strong> k<strong>in</strong>etic energy of the rebound<strong>in</strong>gparticle. For a particle of mass m impact<strong>in</strong>g a surfacenormally with a velocity V im we have1mV 22 im þ Q A ¼ Q E þ Q L ;ð2Þwhere Q A is the energy due <strong>to</strong> the attractive forces betweenthe <strong>in</strong>com<strong>in</strong>g particle and the surface. If the s<strong>to</strong>redelastic energy, Q E , is greater than the adhesive energyrequired <strong>to</strong> separate the particle from the surface, Q 0 A ,then the particle will rebound otherwise it sticks <strong>to</strong> thesurface. The rebound <strong>speed</strong>, V r , is calculated from1mV 22 r¼ Q E Q 0 A : ð3ÞThe mentioned energy terms are described <strong>in</strong> detail byRogers and Reed and <strong>in</strong> van Beek [11]. The maximum


M.S. Abd-Elhady et al. / International Journal of Heat and Mass Transfer 47 (2004) 3943–3955 3953Fig. 12. A comparison between the particle size distribution of the <strong>in</strong>jected glass particles <strong>in</strong> the airflow and the glass particles <strong>in</strong> thefirst foul<strong>in</strong>g layers deposited on the HE tube.Table 2A comparison between the particle size distribution of the <strong>in</strong>jected glass particles <strong>in</strong> the airflow and the glass particles <strong>in</strong> the first foul<strong>in</strong>glayers deposited on the HE tubea b cMean diameter (d M ) Standard deviation (SD) D 10 D 50 D 90Injected glass particles<strong>in</strong> airflowGlass particle <strong>in</strong> thefoul<strong>in</strong>g layer nearthe HE tube20.4 16.2 3.6 16.2 43.114.7 8.4 5.9 13.3 25.2All dimensions are <strong>in</strong> micrometers.a The particle diameter at which 10% of the particles are smaller than it.b The particle diameter at which 50% of the particles are smaller than it.c The particle diameter at which 90% of the particles are smaller than it.impact <strong>speed</strong> at which an <strong>in</strong>cident particle will stick <strong>to</strong>the impacted surface, i.e. V r ¼ 0, is def<strong>in</strong>ed as the criticalstick<strong>in</strong>g velocity. To show the variation of the stick<strong>in</strong>gvelocity with the <strong>in</strong>cident particle diameter the Rogersand Reed model is solved <strong>to</strong> calculate the stick<strong>in</strong>gvelocity for copper particles of diameters 10 and 4 lmhitt<strong>in</strong>g a solid steel surface. Fig. 13 shows the variationof the coefficient of restitution, e, with the impact <strong>speed</strong>,V im , for copper particles of diameters 10 and 4 lm. Thecoefficient of restitution is def<strong>in</strong>ed as the ratio betweenthe normal rebound <strong>speed</strong>, V r , and the normal impact<strong>speed</strong>, V im , for a particle hitt<strong>in</strong>g a solid surface. Fig. 13shows that if a copper particle of diameter 10 lm hits asteel surface at a <strong>speed</strong> lower than 0.025 m/s it will stick,while a copper particle of diameter 4 lm sticks if it hitsat a velocity lower than 0.12 m/s. Therefore, if we have amixture of particles of diameters 10 and 4 lm <strong>in</strong> air,which is flow<strong>in</strong>g with an average <strong>speed</strong> of 1 m/s over aHE tube, there will be a larger number of particles thathit the HE tube with a <strong>speed</strong> lower than 0.12 m/s thanthe number of particles that hits with a <strong>speed</strong> lower than0.025 m/s. This can expla<strong>in</strong> why small particles are likely<strong>to</strong> dom<strong>in</strong>ate at the beg<strong>in</strong>n<strong>in</strong>g of the foul<strong>in</strong>g process.3.4. S<strong>in</strong>ter<strong>in</strong>g of foul<strong>in</strong>g layersOnce foul<strong>in</strong>g has started and particles accumulate <strong>to</strong>build up the foul<strong>in</strong>g layer, s<strong>in</strong>ter<strong>in</strong>g takes place. S<strong>in</strong>ter<strong>in</strong>gchanges the foul<strong>in</strong>g layer structure from a weakpowdery layer <strong>to</strong> a solid stable structure strongly attached<strong>to</strong> the <strong>heat</strong> exchanger tubes [12]. S<strong>in</strong>ter<strong>in</strong>g is afunction of time and of the hot <strong>gas</strong> temperature flow<strong>in</strong>gover the foul<strong>in</strong>g layer [13]. Fig. 14 shows a cross sectionalview for a foul<strong>in</strong>g layer taken from the previousexperiments mentioned above. The particles <strong>in</strong> the layerare bronze and were subjected <strong>to</strong> hot air at 200 °C for


3954 M.S. Abd-Elhady et al. / International Journal of Heat and Mass Transfer 47 (2004) 3943–3955Coefficient of restitution, e = V r / V im.10.90.80.70.60.50.40.30.20.10Stick<strong>in</strong>g limit =0.025 m/sStick<strong>in</strong>g limit = 0.12 m/sdp=10 micrometersdp=4 micrometers0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1 1.1 1.2 1.3 1.4 1.5Impact <strong>speed</strong> V im (m/s).Fig. 13. Coefficient of restitution versus impact <strong>speed</strong> for copper particles hitt<strong>in</strong>g a solid steel surface.Fig. 14. A cross sectional image through the foul<strong>in</strong>g layer, thearrows show the position of the scratches.9 h dur<strong>in</strong>g the foul<strong>in</strong>g experiments. Fig. 2d shows a SEMpho<strong>to</strong> for the bronze particles before usage <strong>in</strong> the foul<strong>in</strong>gexperiments. If we compare Figs. 2d and 14 we f<strong>in</strong>d thatmost of the bronze particles <strong>in</strong> the foul<strong>in</strong>g layer havescratches on the surface compared <strong>to</strong> the <strong>in</strong>itial particles.These scratches are probably the areas of contact whichhave been made up due <strong>to</strong> s<strong>in</strong>ter<strong>in</strong>g and were brokendur<strong>in</strong>g splitt<strong>in</strong>g of the foul<strong>in</strong>g layer for exam<strong>in</strong>ationunder the SEM. S<strong>in</strong>ter<strong>in</strong>g makes removal of the foul<strong>in</strong>glayer by soot blow<strong>in</strong>g afterwards difficult.An experimental setup has been built and developed<strong>to</strong> study the mechanism of foul<strong>in</strong>g over <strong>heat</strong> <strong>exchangers</strong>tubes as a function of flow <strong>speed</strong> and contam<strong>in</strong>at<strong>in</strong>gparticles. Foul<strong>in</strong>g starts at areas that are subjected <strong>to</strong>m<strong>in</strong>imum shear<strong>in</strong>g forces, the rear end of the tubes andthen spreads <strong>to</strong> the circumference due <strong>to</strong> particle transport<strong>to</strong> the already deposited particles. F<strong>in</strong>e particlesstick first <strong>to</strong> the <strong>heat</strong> exchanger tubes because of theirhigher stick<strong>in</strong>g velocity than coarse particles. Then thelarge particles deposit and the foul<strong>in</strong>g layer starts <strong>to</strong>build up. As the flow <strong>speed</strong> <strong>in</strong> the <strong>heat</strong> exchanger <strong>in</strong>creases,the thickness and the surface area of the foul<strong>in</strong>glayer deposited over the <strong>heat</strong> exchanger tube are reduced.The flow <strong>speed</strong> at which foul<strong>in</strong>g ceases is calledthe limit<strong>in</strong>g foul<strong>in</strong>g <strong>speed</strong>. The limit<strong>in</strong>g foul<strong>in</strong>g <strong>speed</strong> iscompared <strong>to</strong> the critical flow velocity required <strong>to</strong> roll aspherical particle rest<strong>in</strong>g on a flat surface and subjected<strong>to</strong> a shear flow. Depend<strong>in</strong>g on the particle size distribution<strong>in</strong> the <strong>gas</strong> flow, f<strong>in</strong>e particles deposited on the HEtube may be removed by the large deposit<strong>in</strong>g particles.The removal of f<strong>in</strong>e particles by the large deposit<strong>in</strong>gparticles leads <strong>to</strong> a lower limit<strong>in</strong>g foul<strong>in</strong>g <strong>speed</strong> than thelimit<strong>in</strong>g foul<strong>in</strong>g <strong>speed</strong>, which corresponds <strong>to</strong> the smallestparticle <strong>in</strong> the <strong>gas</strong> flow. The <strong>in</strong>fluence of the particle sizedistribution on the selection of the limit<strong>in</strong>g foul<strong>in</strong>g <strong>speed</strong>still has <strong>to</strong> be <strong>in</strong>vestigated <strong>in</strong> more detail. To preventfoul<strong>in</strong>g, the <strong>gas</strong> <strong>speed</strong> of a <strong>heat</strong> exchanger should belarger than the critical flow velocity that corresponds <strong>to</strong>the particle size most likely <strong>to</strong> stick first and rema<strong>in</strong> onthe HE tube. As the foul<strong>in</strong>g layer starts <strong>to</strong> build ups<strong>in</strong>ter<strong>in</strong>g takes place. S<strong>in</strong>ter<strong>in</strong>g gradually changes thelayer from a loose powdery structure <strong>to</strong> a more solidstructure strongly adhered <strong>to</strong> the <strong>heat</strong> exchanger tube.S<strong>in</strong>ter<strong>in</strong>g makes it difficult afterwards <strong>to</strong> clean the tubesby soot blow<strong>in</strong>g.4. Conclud<strong>in</strong>g discussionAcknowledgementsWe would like <strong>to</strong> acknowledge the staff members ofthe labora<strong>to</strong>ry of Thermal Eng<strong>in</strong>eer<strong>in</strong>g at the Universityof Twente for their assistance <strong>in</strong> prepar<strong>in</strong>g and perform<strong>in</strong>gthe experiments.


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