HEAT TRANSFER DURING PNEUMATIC TRANSPORT 0F SPRAY- DRIED FOOD PRODUCTS Thesis for the Degree of Ph; D. MiCHéGAN STATE UNEVERSETY. PlE-YI WANG ‘ 1970 LIBRAR Y MlChlgan S i, 5.; University I This is to certify that the thesis entitled HEAT TRANSFER DURING PNEUMATIC TRANSPORT OF SPRAY-DRIED FOOD PRODUCTS presented by Pie-yi ‘Wang has been accepted towards fulfillment of the requirements for Ph.D. Agr. Eng. degree in :91 K. HJLLMM Major professor Date February 26, 1970 O~169 Y BINDING BY ‘ ‘ "DAB & SUNS' 800K BINDERY INC. s IWJI I ABSTRACT HEAT TRANSFER DURING PNEUMATIC TRANSPORT OF SPRAY-DRIED FOOD PRODUCTS By Pie-yi Wang Since spray drying improves the storage of products, reduces the cost of transportation, and provides a product which can be served as a convenience-type food, it is used extensively to manufacture several food products. Dry milk probably is the most widely known spray-dried food product; non-fat dry milk was therefore used as the representative test material. Most of the spray-dried products are subjected to cooling after leaving the drying chamber. In order to effectively control the product temperature, the investigation of heat transfer rate during the processing was needed. In order to predict the temperatures of air and particles, the equations describing the temperatures of air and product particles have been developed based on the enthalpy balance of the system with three different wall conditions; uniform wall temperature, linear wall temperature, and uniform heat flux. Since the mixture heat trans- fer coefficient was employed to develop the governing equations, the mixture Nusselt number was experimentally determined in order to evaluate the derived equations. Only the uniform wall temperature experiments were conducted in this investigation. In the food industry, the spray-dried food products should be cooled immediately after entrance into the air Pie-yi Wang stream. The average mixutre Nusselt number, therefore, was experimen- tally determined at the entrance region. In addition, the mixture Nusselt number was determined for two situations; equal and different inlet temperatures of product particles and air. The experimental results illustrated that there is no significant difference in heat transfer rate between equal and different inlet temperatures. For this reason, the experimental results of both cases were combined to establish the general correlation. The experimental results were correlated to be: G c = 0.61 0.75 (1mm 0.17 (Re)a (1 + -P-—BGaca) (i 77.) This empirical equation is valid for convective capacity parameter greater than unity and within the entrance region with a uniform wall temperature. With the aid of this empirical equation, the temper- atures of air and particles can be predicted from the derived equations. There was no direct method to verify the derived equations of temperature history. The mixture temperature was, however, predicted from the calculated air and particle temperatures and measured by the experiment. Since the predicted and measured mixture temperatures were in agreement, the predicted air and particle temperatures were assumed to predict the true temperature of both phases. This indirect method was used to verify the derived equations. By comparison of the experimental and predicted results, the temperatures of air and product particles were well predicted by the derived equations. Tem- perature histories of product particles were then plotted in charts. Pie-yi Wang Approved Q. R “&W\ 4/99/70 Major Professor iv” M Department Chairman 4/14/70 Date HEAT TRANSFER DURING PNEUMATIC TRANSPORT OF SPRAY-DRIED FOOD PRODUCTS By Pie-yi Wang A THESIS Submitted to Michigan State University in partial fulfillment of the requirements ' for the degree of DOCTOR OF PHILOSOPHY Department of Agricultural Engineering 1970 €22qu 7'17 70 For their personal sacrifice, understanding and encourage- ment, this thesis is dedicated To my wife, Chun Rwang, My newborn daughter, Karin H. Wang, and My mother, Mrs. Lai-hou Wang ii ACKNOWLEDGMENTS The author wishes to express his sincere appreciation and gratitude to: Dr. D. R. Heldman, Associate Professor, Agricultural Engineering Department and Food Science Department, for his constant inspiration, encouragement, interest and guidance. Dr. A. W. Farrall, Professor and Chairman, emeritus, Agricultural Engineering Department, for his encouragement and opportunity to work on thermal conductivity measurement of dry milk and field performance of dry milk cooling and storage systems. Dr. A. M. Dhanak, Professor, Mechanical Engineering Department, for his depth and thoroughness in teaching heat transfer at the graduate level and serving as a guidance committee member. Consultations were freely given and most rewarding. Dr. F. W. Bakker-Arkema, Associate Professor, Agricultural Engin- eering Department, for his depth and thoroughness in teaching bio- processing engineering and serving as a guidance committee member. Dr. T. I. Hedrick, Professor, Food Science Department, for consultations and serving as a guidance committee member. Dr. C. W. Hall, Chairman and Professor, Agricultural Engineering Department, for the graduate assistantship that enabled the author to undertake this investigation. iii ACKNOWLEDGMENTS. . . LIST OF LIST OF LIST OF FIGURES. . . TABLES . . . APPENDICES. . NOMENCLATURE. . . . Chapter I. II. III. VI. INTRODUCTION . OBJECTIVES. . LITERATURE REVIEW AND JUSTIFICATION TABLE OF CONTENTS Particle to Fluid Heat Transfer. Relative Velocity between Particle and Fluid Heat Transfer from Wall to Gas-Solids Mixtures. Fluid Mechanics of Gas-Solids System . DEVELOPMENT OF THEORY . Assumption and Justification. l. Fluid and Particle Properties are Independent of Temperature 2. The Particles are Sufficiently Small to Allow the Assumption of no Temperature Gradient Within the Particle. 3. Heat Transfer from the Pipe Wall to the Parti- cles is Negligible . 4. Particles are Uniformly Dispersed and Reach Their Terminal Velocity at the Entrance 0 Position of the Heat Exchanger . ‘ 5. Velocity Profile is Plug-like 6. Nb'Mass Transfer Occurs Mathematical Models. Case 1. Case 2. Case 3. Uniform Wall Temperature Linear Wall Temperature. Uniform Heat Flux. iv Page iii vii viii ix ll 15 16 16 l6 l7 l7 17 18 18 18 19 24 26 Chapter Page v I mpERmEmAL O O O O O O O O O O O O O O O O 29 Experimental System. . . . . . . . . . . . . 29 Particle Feed and Recovery System . . . . . . . 29 Air Metering! . . . . . . . . . . . . . . 31 Heat Transfer System. . . . . . . . . . . . 31 Temperature Measurement . . . . . . . . . . . 33 Experimental Procedures . . . . . . . . . . . 37 Product Characteristics . . . . . . . . . . . 39 VI. RESULTS AND DISCUSSIONS . . . . . . . . . . . . 42 Heat Transfer Results . . . . . . . . . . . . 42 Temperature Histories . . . . . . . . . . . . 51 VII. ANALYSIS. .. . . . . . . . . . . . . . . . . 62 VIII. CONCLUSIONS . . . . . . . . . . . . . . . . 78 IX. RECOMMENDATIONS FOR FUTURE WORK. . . . . . . . . . 79 BIBLIOGRAPHY. . . . . . . . . . . . . . . . . . . 81 APPENDICES...................86 Figure 5.1 5.2 5.3 6.1 6.2 6.3 6.4 6.5 6.6 6.7 6.8 6.9 7.1 LIST OF FIGURES The System Investigated. . . . . . . . . . . Experimental System . . . . . . . . . . . . . Experimental Nusselt Number of Air Compared with Kreith Proposed Equation for Constant wall Temperature. . Locations of Thermocouples. . . . . . . . . Mixture Nusselt NUmber vs. Reynolds for Various Convective Capacity Parameters . . . . . . . . . . . . . Mixture NUSselt Number vs. Convective Capacity Parameter for Various Reynolds Number With Equal Inlet Temperature. Mixture Nusselt Number vs. Convective Capacity Parameter for Various Reynolds Number With Different Inlet Temper- ature. O O O O I O O O O O O O O O O O O The Combined Nusselt Number vs. Convective Capacity Para- meter. 0 C C O O O O l. O O . O O I O C 0 Comparing the Measured Outlet Temperatures of Mixture with the Predicted Temperatures of Particles, Mixture, and Air for (Re)a = 5.6 x 104 . . . . . . . . . . . . Comparing the Measured Outlet Temperatures of Mixture with the Predicted Temperatures of Particles, Mixture, and Air for (Re)a = 5.6 x 104 I I O C O O O O O O O O Thermocouples Locations at the Exit Position With Its Represented Areas. . . . . . . . . . . . . . Comparing the Measured Outlet Temperature of Particles and Mixtures with the Predicted Temperatures of Particles, Mixture and Air for (Re)a = 5.6 x 104 . . . . . . . Comparing the Measured Outlet Temperature and the Measured Mixtures Temperature With the Predicted Temperatures of Particles, Mixture, and Air for (Re)a = 4.7 x 10 . . Temperature Histories vs. Axial Distance under the System of Adiabatic Condition and Uniform Wall Temperature for Loading Ratio of 0.56 and Reynolds NUmber of 5.6 x 104 . vi Page 20 3O 34 38 45 47 48 50 54 55 58 59 60 65 i.— I—“. l.l Figure Page 7.2 Dimensionless Temperature History of Particles Along the Axial Distance during Pneumatic Transport of Spray-Dried FOOd PrOduc ts O O I O O O O O O O O O O O O O 74 7.3 Dimensionless Temperature History of Particles Along the Axial Distance during Pneumatic Transport of Spray-Dried Food Products . . . . . . . . . . . . . . . . 75 7.4 Dimensionless Temperature History of Particles Along the Axial Distance during Pneumatic Transport of Spray-Dried Food Products . . . . . . . . . . . . . . . . 76 7.5 Dimensionless Temperature History of Particles Along the Axial Distance during Pneumatic Transport of Spray-Dried Food Products . . . . . . . . . . . . . . . . 77 vii Table 6.1 7.1 LIST OF TABLES page Characteristics of Heat Exchanger. . . . . . . . . . 35 Comparison of the Predicted and Measured Mixture Temperature (Different Inlet Temperature) . . . . . . . . . . . 56 The Outlet Temperatures of Particles at the Exit Position of a 10 ft. Conveying Tube under Various Loading Ratios and Dif- ferent wall Conditions, (°F) . . . . . . . . . . . 69 viii LIST OF APPENDICES Appendix Page A. Solutions for the Case of Uniform Wall Temperature. . . . 87 B. Solutions for the Case of Linear Wall Temperature . . . . 92 C. Solutions for the Case of Uniform Heat Flux . . . . . . 97 D. Experimental Results (Equal Inlet Temperature) . . .. . . 100 E. Experimental Results (Different Inlet Temperature . . . . 102 F. Measured and Predicted Temperatures (Equal Inlet Temper- attire. o o o o o o o o o o o o o o o o o o 1.03 ix 4. ni» NOMENCLATURE Experimental constant. Particle surface area as defined in equation (5-6), ft2.ft3. Individual particle surface area, ftz. Tube wall thickness, ft. n = l, 2, 3, 4, 5, 6, parameters as defined in Appendix A. Experimental constant. n = l, 2, 3, 4, integration constant. Specific heat of air, Btu/lb-°F. Drag coefficient. Specific heat of particle, Btu/lb-°F. Particle diameter, ft. Small or large tube diameter, ft. Tube diameter, ft. (D1+D2)/2, equivalent diameter, ft. Experimental constant. 2 Gravitational constant, ft/sec . Vapa, Mass flow rate of air, lb/hr-ftz. Vppp, Mass flow rate of particles, lb/hr-ftz. Heat transfer coefficient of air alone, Btu/hr-ft2-°F. Heat transfer coefficient of air at the entrance region, BtUIhr-ft2-°F o (NU)m (mop (Nu)w Pr Heat transfer coefficient of gas-solids mixture, Btu/hr-ft2—°F. Water side heat transfer coefficient, Btu/hr-ft2—°F. Thermal conductivity of air, Btu/hr-ft-°F. Thermal conductivity of particle, Btu/hr-ft-°F. Thermal conductivity of water, Btu/hr-ft-°F. Tube length, ft. ELL) , operator. dx Experimental constant Mixture Nusselt number as defined in Appendix A. hpdp/ka, particle Nusselt number. the/kw’ water side Nusselt number. Capa/ka, Prandtl number Radius from center of tube at the subscribed locations (showed in Figure 11), ft. Mixture side resistance, hr-ft2-°F/Btu. . 2 . Overall resrstance, hr-ft - F/Btu. Tube wall resistance, hr-ft2-°F/Btu. Water side resistance, hr-ft2-°F/Btu. Reynolds number for air alone. Modified particle Reynolds number. Vd/ r P a’ particle Reynolds number. V D / , water side Reynolds number. w e a xi (St)a (St)m (St)d ai 30 mi mo pi p0 . 2 Cross-sectional area of tube, ft . n = l, 2, 3, 4, sub-divided cross-sectional area according to Figure 11, ftz. Stanton number for air alone. Mixture Stanton number as defined in Appendix A. Particle Stanton number as defined in Appendix A. Air temperature, °F. Air inlet temperature, °F. Air outlet temperature, °F. Mixture temperature, °F. Mixture inlet temperature, °F. Mixture outlet temperature, °F. Particle temperature, °F. Particle inlet temperature, °F. Particle outlet temperature, °F. n = l, 2. ......... 12, temperatures with respect to the thermocouples locations as indicated in Figure 4, °F. Wall (or water) temperature, °F. Logarithmic mean temperature difference, °F. Overall heat transfer coefficient, Btu/hr-ft-°F. Air velocity, ft/sec. Individual particle volume, ft3/1b. xii Particle velocity, ft/sec. Relative velocity between particle and air, ft/sec. Free fall terminal velocity, ft/sec. Convective capacity ratio as defined in Appendix A. Axial distance, ft. Particular solution. Complementary solution. Parameter as defined in equation (7-3). Constant, axial temperature gradient, °F. Parameter as defined in Appendix A. Dynamic velocity of air, lb/sec«ft. (T .)/(Tpi-Tw) pi-Tai Kinematic viscosity of air, ft2/sec. Air density, lb/ft3. Particle density per unit volume of mixture as defined in equation (5-7), lb/ft3. True particle density, lb/ft3. Mixture density, 1b/ft3. Shape factor. xiii CHAPTER I INTRODUCTION Spray drying plays an important role in food processing, since it improves the keeping quality of products, reduces the cost of transportation, and provides a product which can be served as a convenience-type food. Spray drying is used extensively to manufac- ture several products such as tomato powder, orange powder, bean pow- der, etc. Probably the most widely known spray-dried product is dry milk. Non-fat dry milk, therefore, was used as the test product in this investigation. The quality of spray-dried food products may be decreased considerably by prolonged storage at high temperatures. In most cases, the prolonged heating causes heat damage. Hall and Hedrick (1966) indicated that the continued heating causes staleness in non-fat dry milk flavor and causes the melted fat to move to the surface of whole milk powder. Heat damage such as clumping, off-flavor, and off-color may develop very rapidly. Hanrahan gt El. (1967) illustrated that slow cooling results in a cooked or scorched flavor in spray-dried milk. Most dry milk plants prefer the milk powder to be cooled below 80° F as indicated by Farrall _£ 31. (1968 b). tha _5 a1. (1966), Farrell 25 11° (1968 a) and Chen (1969) showed that the dry food pro- ducts possess a very low thermal conductivity. The cooling rate in the package, therefore, will require several days to reach the ambient temperature. It would appear that cooling rate during storage is not suffi produ to ca the p dmer mix h pneum rate . ature order conve; illus heate. is on effec temps aPPro. sufficiently rapid to prevent heat damage. Since spray drying utilizes hot air as drying medium, the dried product leaving the drying chamber is at a sufficient high temperature to cause heat damage. For the purpose of maintaining high food quality, the products should be cooled as rapidly as possible after leaving the dryer. As indicated by Farrall _£,§l° (1968 b) most dairy plants mix hot powder with room temperature air and the mixture is then pneumatically conveyed through a tube to the collectors. The cooling rate of this type of system depends mainly on the ambient air temper- ature. Slow cooling rates can be expected during summer season. In order to obtain low temperature products, drying plants may utilize conveying tubes which may be longer than 100 ft. Heldman _£ 31. (1969) illustrated that the rapid cooling rate can be achieved by mixing heated powder with cooled air. However, the direct cold air injection is only effective for low loading ratios. In order to obtain a more effective cooling system for high loading ratios, reduction of surface temperature of the conveying tube seems to offer the most satisfactory approach. CHAPTER II OBJECTIVES The application of gas-solids mixture as a heat transfer and transport media was first used in petroleum-cracking plants. The evidence that solids in gaseous heat transfer systems increased heat transfer rate was found experimentally by the petroleum industry. In this decade, the technique has been utilized in the field of solid propellent combustion, cooling nuclear power plants, food processing, etc. The increasing interest has emphasized the study of heat trans- fer and fluid mechanics of the gas-solids mixture systems. Farbar and Morley (1957) were the first investigators in this field. Due to the lhnited number of investigations and the complexity of the flow mechanism, most available information is based on experimental results. Heat transfer data are limited to: (1) within the fully developed region (aerodynamically) and (2) the equal inlet temperature of gas and particles. In the food industry, powder cooling will begin immediately after entrance to the air stream and a temperature gradient should be main- tained between the two phases. It is necessary to investigate the heat transfer mechanisms within this entrance region and with the different inlet temperatures of the two phases. The objectives of this research were to (1) determine heat trans- fer coefficients between mixture and tube wall within the entrance region, (2) investigate whether the different inlet temperatures in the two phases influence heat transfer coefficients, and (3) develop the mathematical models to predict the temperatures of both air and product particles. The final objective of this investigation was to use the experhmental heat transfer coefficients and the derived equations to analyze different cooling systems for spray-dried food products. CHAPTER III LITERATURE REVIEW AND JUSTIFICATION Zenz and Othmer (1960) presented an extensive literature review of both fluid and heat transfer mechanisms in pneumatic conveying systems. Before 1960, most investigations were experimental in nature. The book, "Fluid Dynamics of Multiphase Systems," by $00 (1967) describes both fluid dynamics and heat transfer mechanisms in the multiphase systems. In this book the continuous mechanics of a single-phase fluid is extended to the multiphase systems. The general equations of motion and energy have been developed. Due to the complexity of fluid dynamics of multiphase, the theoretical solutions are limited to a few simple cases. The following literature review discusses each parameter involved. Particle to Fluid Heat Transfer When a rigid sphere at a given temperature is submerged in a quiescent fluid at another temperature, heat transfer takes place only by conduction through the boundary layer surrounding the particle. For very small particles under free convection, it is known that the boundary layer is appreciably larger than the particle radius. Based on this assumption, Themelis t_§l. (1963) derived the theoreti- cal solution in which the particle Nusselt number is described as: h d (Nu)p - {-2 = 2 ---------------------------------------- (3-1) a Equation (3-1) is appliable only when dp is greater than the mean free path of molecules of the surrounding medium. Since relative motion of the fluid to the particle exists, the heat transfer rate depends on the relative velocity. If the motion of particle falls within Stokes regime, i.e. Reynolds number less than one; Breiman (1952) theoretically derived Nusselt number as a series expansion form: _ l _1_ 2 2 (Nu)p - 2 + 2 (Re)pPr + 6(Re)p Pr + ------------------ (3-2) Equation (3-2) asymptotically approaches the value of 2, corresponding to the conduction in quiescent fluid as described by equation (3-1). For the high particle Reynolds number, theoretical analysis is very complex. Only experimental correlations were conducted within the intermediate and Newton's Law regimes. From literature reviews of Rowe 35 31. (1965), $00 (1967) and Rubnek £5 21- (1968), most of forced- convection heat transfer data for single particle have been correlated in the following forms: (Nu)? = 2 + f(Re): (Pr)c -------------------------------- (3-3) (Nu)p = f(Re): (Pr)C ------------------------------------ (3-4) where a, f, and c are experimental constants. For the low particle Reynolds number, Nusselt number takes the form of equation (3-3). The advantage of using equation (3-3) is to allow description of the heat transfer rate for the particle in quiescent fluid. Various correlations were made by Zenz t 1. (1960) and $00 (1967). The latter suggested that the best fit was proposed by Drake (1961), 0.55 0.33 (Nu)P = 2 + 0.459 (Re)p (Pr) ------------------ (3'5) for l < (Re)p-< 70,000 and 0.6 < Pr < 400 Whether the heat transfer mechanisms of single particle can be extended to multi-particle system is still unclear. Heat transfer data on multi-particle systems obtained by Johnstone gt a1. (1941) and Joukovski gt 31. (1940) were reported by Zenz and Othmer (1960). They indicated that there is some departure from any asymptote at (Nu)p = 2 for low particle Reynolds number, but 800 (1967) concluded that the deviation is not significant. For dilute transport the void which is defined as the volumetric ratio of particles to air stream is greater than 99%. Due to the large void, each individual particle can be assumed to be isolated from the others. It is reasonable,therefore, to employ equation (3-5) for multi-particle system in dilute transport. Relative Velocity Between Particle and Fluid As indicated in the previous section, heat transfer during pneumatic conveying is influenced by the particle Reynolds number: Vd (Re)p = _I;£ V a which is based on the relative velocity, V = V - V r a p Particle motion in fluid can be classified into three regimes: (l) Stokes law regime, (2) intermediate regime, and (3) Newton's Law regime. In any regime, the particle velocity depends mainly on the drag force. Description of the drag coefficient is therefore the necessary condi- tion to derive particle velocity. Within the Stokes law regime, Stoke (1850) obtained the drag force from the Navier-Stokes equations. The drag coefficient was derived as: 24 cD = (Re)p For the case of a free falling sphere, the terminal velocity given by Stokes law is: 2 I d - v gimp pa)g t 18 “a ------------------------------------- (3-6) Allen (1968) indicated that equation (3-6) can apply only to the particle Reynolds number less than 0.2. Within the intermediate regime, Ossen((cited by 500, (1967)) obtained the drag coefficient as: 24 C a: D R ( e)p 3 (1 +'IE (Re)p) ------------------------------ (3-7) for (Re)p < 5. Schillar and Nauman (1933) fitted the experimental values of CD and (Re)p to obtain an empirical equation: = 24 _ 0.687 CD (RE); (1 0.15(Re)p > ------------------------ (3-8) for 01< (Re)P-< 700. Since a unique relationship exists between CD and (Re)p, it is impossible to evaluate Vr from equation(3-7) or equation (3-8) by knowing dp. Jones t l. (1966) gave the empirical formula of relative velocity in this regime, I 0.673 1.02 2.4 - d v = (DP pa) ( ) (x) r 0.7 ----------------- (3-9) 0.372 0.347 pa Fla Heywood (1962) combined Stokes and Newton's law with a graphical solution and constructed tables. From Heywood's Tables, terminal velocity can be obtained by knowing dp. Within Newtons law regime, the drag coefficient has been confirmed to be 0.44. Belden and Kassel (1949) suggested the formula for relative velocity as: I vr 1.32 «fgdp (pp - pa)/ pa ---------------------------- <3-10) Tchen (1947) studied the motion of a particle suspended in a turbulent stream using the assumption that the resistance was described by Stokes law and derived an analytical equation for the mean square relative velocity. For estimating the equation, turbulent intensity has to be determined. $00 (1967) determined that the Reynolds number of a 50 micron diameter carbon particle which was suspended in turbulent air flow was 2.52 based on Tchen's result and 0.53 based on the free fall terminal velocity from Stokes law. This comparison indicates that the free fall terminal velocity cannot be used for evaluating relative velocity of particles conveyed in a turbulent stream. - 10 - For the multi-particle system, Hinkle (1953) used a high speed photographic technique to study the relative velocity in gas-solids mixture systems and expressed an empirical relationship as: _ 0.3 I 0.5 Vr 1.4 Vadp (pp / pa) ---------------------------- (3-11) These results indicate that the loading ratio does not affect the relative velocity. Hariu and Malstod (1949) and Wen and Simons (1959) investigated the relative velocity during dense phase transport (high loading ratio) and concluded that the air velocity is approximately double the particle velocity: Va 2: zvp ------------------------------------------------ (3-12) The loading ratio used by Wen S£.§l' (1959) and Hariu _£ _1. (1949) ranged from 80 to 750 and 2 to 18, respectively. By comparison of the particle Reynolds numbers obtained from single particle and multi-particle systems, it appears that the particle Reynolds number of multi-particle system is much greater than that of the single particle case. The deviation is obviously due to the momentum transfer of particle collisions with wall and other particles in the multi-particle system. However, Wen and Miller (1961) and Yannopoulos gt 31° (1966) suggested that free fall terminal velocity can be used to evaluate the relative velocity in gas-solids mixture systems. According to Tchen's (1947) and Hinkle's (1953) investiga- tions, the application of the free fall terminal velocity to gas-solids mixture systems is questionable. _ 11 - There is an obvious lack of information about the relative velocity within an acceleration region. Hariu £5 31. (1949) and Hinkle (1953) concluded from their investigation of the pressure drop that the distance of 14 feet is required for particles to attain a constant velocity. Zenz and Othmer (1960) analyzed Russ and Culgan's data (1950) and concluded that the acceleration rate increases as loading ratio decreases. At high air velocities and low loading ratios, the total acceleration distance is only about two feet. Allen (1968) presented the following statement: " It can be shown that under the conditions likely to be found in sedimentation of elutriation, the assumption that the terminal velocity is reached instantaneously introduces a negligible error." Heat Transfer From Wall To Gas-Solids Mixtures Heat transfer in gas-solids suspensions within a confining vessel has been the subject of many studies because of the addition of suspended particles having not only the advantage of higher heat capacity, but also that of promoting heat transfer rate. The first investigators in this field, Farbar and Morley (1957), illustrated that the reasons for increased heat transfer rate due to adding particles to an air stream are (l) the high volumetric specific heat of the solid particles and (2) the reduction of the boundary layer thickness. In addition, they found there exists a critical loading ratio of unity. Above the loading ratio of one, heat transfer rate is consider- able increased. The heat transfer rate increases only slightly, however, when the loading ratio is less than unity. They correlated - 12 - the experimental results and give the mixture Nusselt number as: (Nu)... = 0.14 (Re)2°6 (GP/ca)°°“5 ------------------------ (3-13) for (Gp/Ga) > 2 Tien and Quan (1962) and Jepson and Smith (1963) conducted additional investigations and indicated that, due to inertia, the introduction of particles reduced the scale of turbulence of the gas as long as the loading ratio was between zero and one. Above a loading of unity, turbulence was increased. Results from Farbar and Morley (1957) and Jepson and Smith (1963) are shown in Figure 3.1 and 3.2. The investigations of previous researchers and several others which will be mentioned later are limited to the fully developed region (aerodynamically) as well as equal inlet temperatures of air and particles. Danziger (1963) correlated the data of air-catalyst mixtures in vertical transport and presented a correlation, DG = a 0.66 (Nu)m 0.0784 (13-) (GP/Ga)0’4S -------------------- (3-14) a 2 for (GP/Ga) > Equation (3-14) is in good agreement with equation (3-13). Tien (1961) made the first analytical attempt to predict the effect of the addition of solid particles to an air stream on the heat trans- fer coefficient. A solution was obtained for the constant wall temperature, which was then extended to the case for arbitrary wall temperatures. The limitations of Tien's analytical solutions are: (1) particle and air are assumed to be at the same velocity, Mixture Nusselt Number (hmD/ka) 200- m Heat Transfer Coefficient - h _ 13 - Figure 3.1 Mixture Nusselt number vs. solids loading for constant air flow rates ((Farber and Morley (1957)). 00 - - 80 - (Re)a - 27 000 _"///,/////////zzzrr 60 - ‘ 13,500 I l l L 0.1 0.5 1.0 2 4 6 Solid Loading Ratio -- (GP/Ga) J.“ O A w (0 v O) I 11 = 60 ft/sec Va = 40 ft/sec 2 l I 1 l l I l 0 2 4 6 8 10 12 14 Solids/Air Loading Ratio -- (GP/G ) a Figure 3.2 Heat transfer coefficients at various solids loading ratios((Jepson and Smith (1963)) - 14 - (2) particle and air are at the same inlet temperature, and (3) the flow must be fully developed. Wen et al. (1961) correlated several investigators' results and gave the equation, m C h = E£(pm/pp)°°3 (Vt/gdp)0'21 ------------------------- (3'15) P As discussed in the previous section, since the free fall terminal velocity of single particle is utilized in the multi-particle system, the validy of the equation (3-15) may be questionable. Farber gt 31. (1963) and Jepson _£.a1. (1963) investigated the effect of particle size on the heat transfer coefficient. Both investigators indicated the same relationship that the increase in particle diameter reduces the heat transfer coefficient. The maximum diameter for increased heat transfer coefficients were determined as 200 micron and 500 micron for glass beads and sands, respectively. For the case of constant heat flux, Depew and Farbar (1963) derived an analytical solution forthe mixture Nusselt number utilizing techniques similar to Tien (1960). The limitations are the same as Tien's solutions. In the work sponsored by the Atomic Energy Commission, a group at the Babcock & Wilcox Co., Atomic Energy Division (1959) studied flowing gas-solids mixtures as a heat transfer media, using finely divided graphite with nitrogen, helium, and Freon 14. In their final report, they presented a correlation of their data for heat transfer from an electrically heated tube to gas-solids mixtures vertical flow with the equation, 0.802 c c 0.45 (Nu)m = 0.0195 ((Rea) Pr)) (1 + 5953) ---------- (3—16) 88 - 15 - Wilkinson and Norman (1967) presented heat transfer data obtained in a vertical heated tube on suspensions of glass beads and graphite in the air. A plot of (Nu)m/(Re)3'8 versus Tw/Tm revealed a negative cube root dependence. Fluid Mechanics of Gas-Solids Systems Fluid mechanics of gas-solids systems is complex with respect to the distribution of particles across the pipe and the velocity pro- files of both phases. $00 and Regalbutp (1960) summarized their investigation with the following statement: "Due to the inertia of solid particles, transport of solid particles across the velocity field of the turbulent stream by turbulent diffusion results in deceleration of particles in the region near the wall by the stream and acceleration of particles transported toward the high velocity core. In the core, the particles have lower mean velocity than the stream while near the wall the mean particle velocity is higher. This gives rise to a non-uniform distribution of solid particles in fully developed turbulent pipe flow." However, Soo'_t al. (1960) indicated that the constant distribution can be assumed for the low loading ratio, high stream velocity, and small particle size. Depew, gt al. (1963) indicated that due to a non- uniform distribution of particles, the velocity profile will be affected. The~change could be either toward a more plug-like or a more streamline profile. 800 (1967) showed that within the range of loading where the presence of solids contributes to lowering of friction factor in fully developed turbulent pipe flow, the velocity profile of the gaseous phase was unaltered. - l6 - CHAPTER IV DEVELOPMENT OF THEORY Assumption and Justification Due to the complexity of the fluid mechanics of gas-solids mixture systems, the analytical solutions for the temperatures of air and particles are very difficult to obtain. Tien (1960) attempted to solve the problem of utilizing the single phase techniques which were employed by Sleicher _£ 31. (1957). Tien (1960), however, found that insufficient mathematical theory has been developed for its solution. For the case of adiabatic conditions, Sissom t l. (1965), Bakker-Arkema 35 21. (1969) and Heldman £5 31. (1969) have developed the mathematical expressions to evaluate the temperatures of both phases. The former dealt with the dense transport; the latter considered the dilute conveying. All investigators have assumed the system to be plug flow in order to simplify the complexity. For the arbitrary wall conditions, the following basic assumptions are utilized: 1. Fluid and Particle Properties Egg Independent pf Temperature. Thermal properties of fluid or particles are usually a function of temperature. However, thermal properties can be assumed constant if the temperature range is small and the bulk mean temperature is used to evaluate the properties. This assumption has been utilized previously in general heat transfer calculations. - 17 _ 2. The Particles are Sufficiently Small £9 Allow the Assumption 9f ‘Np Temperature Gradient Within the Particles. This assumption can be checked with the lumped-capacity proposed by Holman (1968): h V b d lumped-capacity == RBAQ = 35-2 P P P where V0 and Ap are individual particle volume and surface area respectively. The distribution of particle sizes of non-fat dry milk has been investigated by Hayashi _£ 31. (1967). The average diameter was determined to be 60 micron. Particle heat transfer coefficients can be evaluated with equation (3—5). At a particle Reynolds number of 10 which is an approximate value in this investiation, hp was calculated to be 250 Btu/hr—ft2 - °F. From Chen's investigation (1969) the thermal conductivity of the non-fat dry milk particle was measured as 0.26 Btu/hr-ft-°F at 3.5%.moisture content and 100° F. By the substitution of the values of hp, dp, and kp, the lumped-capacity was calculated to be 0.068 which is less than 0.1 and meets the assumption of no temperature gradient. 3. Heat Transfer from the Pipe Wall £9 Ehg Pargiglg§.i§_gegligiplg. Farber and'Morley (157) indicated that due to small contact area between particle and wall as well as short contact time, the possibility of any heat transfer from the pipe wall directly to the particles can be eliminated. 4. Particles are Uniformly Dispersed and Reach Their Terminal Velocigy 25 Eh; Entrance Position_gf the Heat Exchanger. The distribution of particles across the cross section of a - 18 - conveying tube and the acceleration of particles have been discussed in previous sections of Chapter 3. This assumption appears to be valid for the conditions of low loading ratio, high average stream velocity, and small particle size. 5. Velocity Profilg lg Plug-Like. The plug flow is usually considered to be a first approximation in turbulent or non-Newtonian flow. It is readily seen that this assumption is considerably different from the actual case. However, in the case of entrance regions or turbulent pipe flow, at least a major portion of the tube cross section approaches plug flow. 6. .N9 Mass Transfe; Occurs. Spray-dried products are maintained at low moisture content. Adsorption or desorption occurs only during the falling rate period if the products are exposed to the air stream of low relative humidity. Since mass transfer during the falling rate period is small, it can be neglected if the retention time of particle in the air stream is short. It can be realized that the latent heat of water vapor is approximately 1000 Btu/1b. If mass transfer occurs during the process, the temperature history of particles and air must be affected signifi- cantly. Mathematical Models The following analysis will deal with three different wall condi- tions; (1) uniform wall temperature, (2) linear wall temperature, and (3) uniform heat flux. By derivation of equations which describe both the enthalpy content of the air and the particles as the mixture moves through the conveying tube, the change in temperatures of air and particle The proc temperat uniform presente (i) Ent By as a ref The Chan differen Va; As the a tlansfe] air, the The Met _ 19 - particles can be predicted based on properties of air and particles. The procedures for setting up the governing equations of linear wall temperature or uniform heat flux case are similar to those of the uniform wall temperature case. The detailed development will be presented in the latter case only. Case 1. Uniform wall Temperature (i) Enthalpy balance of air By using a control volume within the conveying tube (see Figure l) as a reference, the enthalpy of air entering the control volume de is: VapaCaSTadx ---------------------------------------------- (4-1) The enthalpy of air leaving de is: dTa Vapacasaa + ‘33:) dx ------------------------------------- (4-2) The change in enthalpy of air with respect to axial distance is the difference between equation (4-2) and (4-1), or dTa Vapacasig ----------------------------------------------- (4-3) As the air moves through the control volume, two types of heat transfer may occur. The first is the convection between wall and air, the other is the convection between air and solid particles. The heat flux from pipe wall to the gas-solids mixture is defined by: qw = hmpn ('rw - rm) dx ----------------------------------- (4-4) 20 - .woumwmumo>cw Eoummw mLH H.¢ muswflm lLsTl u)— NQG> nl.l.lil oEDHo> Houucoo a a IAIIIII. HH< q>,_ moHuHuumm Th1 mixi T m l The ent! particln qp Tne tote then, - 21 - The mixture temperature Tm is defined as: V p C T + V p C T T = a a a a P P P P ________________________________ (4_5) m V p C + V p C see PPP The enthalpy change resulting from the heat transfer between air and particles can be written as: qp = hpAS (Ta - Tp)dx ----------------------------------- (4-6) The total change in enthalpy of air within the control volume is then, dT a .. - - - _ vapacasdx dx hm"D(Tw Tm)dx hpAS(Ta Tp)dx (4 7) Since 8 is cross-sectional area of the pipe, it can be represented by: 2 =32. ................................................ .. s 4 (4 8) By substitution of equation (4-8) into (4-7), a new equation is obtained: dTa 4hm h A 71;- = m“. ' Tm) ‘ 4"“; p c (T. ' T.) """""""" (4'9) a a a a a a (ii) Enthalpy balance for solid particles The enthalpy of solid particles entering the control volume de is: V C ST dx --------------------------------------------- 4-10 pppp P ( ) The enthalpy of solid particles leaving the control volume de is: dT v csr+——de ..................................... 4-11 pppp(p dx) ( ) The enthalpy change of solid particles with respect to axial direction is the difference between equation (4-11) and (4-10), or dT v c s—P-dx -------------------------------------------- 4-12 app 9 dx ( ) The cha de res- neglect (4-6). d1“ EC Equation Boundary With the t0 Obtai‘ ”vs” ”C ,_.- - 22 - The change in enthalpy of solid particles within the control volume de results from the energy transmitted from air to particles by neglecting the effect of the wall to particles is similar to equation (4-6). Combining equation (4-6) and (4-12) gives: dT h A de -- —P——Vpppcp (Ta -Tp) -------------------------- “'13) Equation (4-9) and (4-13) are the governing equations of the system. Boundary conditions of the system under study are: r'Tp = Tpi x=o, 1T”. ------------------------------------ (4-14) a a1 With the boundary conditions, the governing equations can be solved to obtain: (see Appendix A) T - T (St) _£L___2L. = (.____e_ ) ( A ) Tpi - Tw w ¢(l+w) (sc)d 4(St)m w ' (1+w) T i - Tai 4(St)m x {[(W)'('fp‘."-—i—)3EXPE’WBJ‘ p1 w 4w(St)m 0(l+w) (St)d x [ o<1+w) (sc)d . 51} T . - T . 1 Exp [- pi w ......................... (4-15) In the 1 14-15) - 23 - - Tw (St)d ___a___=_____ D Tpi - Tw ( w ) (0(1+w) (St)d 4(sr)d) w ' (1+w) T i - Tai 4(St)m x {W 1 (1 + W) - (EEj-:—§—-) ] EXP 1 - 73;;3- '5 J - pi w 4w(St) 4w(St) T . - T . [l‘ouw “‘ ”101+. “‘ _(_,.___._,H ( ) (St)d ( ) (St)d Tp1 - Tai P(l+w) (St)d x 1 Exp [ - - J r ------------------------- (4'16) w J In the case of the equal inlet temperatures of both phases, equation (4-15) and (4-17) are simplified as follows: T - TW (St)d 0 T . - T = ( w ) ( 0(1+w) (St) 4(St) ) p1 w d - m w (1+w) 4(St)m x 4w(St)m { (1+w) EXP [ ' 7I¥§3_' B J ' [ D(1+W) (St)d J 0(l+w) (St)d x Exp E - w ~15 1 } --------------------------- <4-17) ———-—Ta - T“ = <——(St)d) ( 0 ) Tpi - Tw w ¢(1+w) (St)d - 4(St)m w (1+w) 4(St)m x 4W(St)m 1 - — - - i“ MEX" [ (1+w) D J L 1 ¢(1+w) (sod 3 4w(St)m 0(l+w) (St)d x ~ _ 1 L 0<1+w) (socl 3 EXP L ‘ w n J J ............................ (4-18) 918:2- Ac I wall te: T w By fol}? for air (i) Enfl The (4'9). 0f equat PGIature - 24 - Case 2. Linear Wall Temperature According to Sleicher, _£._l. (1957), the definition of linear wall temperature is: Tw = Tai - (1x ------------------------------------- (4‘19) By following the same procedures as for Case I, the enthalpy balance for air and solid particles can be obtained. (i) Enthalpy balance for air The governing equation for air temperature is similar to equation (4-9). The only difference is the wall temperature. By substitution of equation (4-19) into equation (4-9), the new equation for air tem- perature is obtained: dTa 4hm h A (T ”fax-T)- ai m dx =VpCD a a 3 (ii) Enthalpy balance for solid particles The heat transfer mechanism between air and particles is as same for the case of uniform wall temperature. Equation (4-13), therefore, is employed here as follows: dT h A de = —P———vpppcp (T. - 'rp) ---------------------------------- <4-21) Equation (4-20) and (4-21) are the governing equations of the linear wall temperature system. Boundary conditions of this system are: {_T = T i x = 0, P P -------------------------------------- (4-22) Ta = Tai with t to obt LH - 25 - With these boundary conditions, the governing equations can be solved to obtain: (see Appendix B) w (St) (—————— + -——JP 4(St)m 4 E l 0(St)d 4(St) ] 0(St)d + - m w (1+w) w(T - T .) D(St)d 4(St)m W ‘0(1+w) (St)d ) + pi a1 ______ _ ______ _ _ _ {t at, ( (1+w) > (1 w) W ““5”... one.) (51;)d 2 J Exp ( - 0(1+w) (St)d w T - T . x W (St) _£____2l =._ m a1) D + (4(St)m + 4 E l ¢(St)d 4(St)mJ ”(3% " —w— ' (Tm— {L‘Za'_.1(___- D w (1+w) 4w(St) ¢(1+w) (soc1 Ill T . D(St)d 4(St)m ) _) } ------------- (4-23) D W o<1+w) (St)d + X — ) 1 -------- (4-24) J Exp ( - w o<1+w)2 Exp < - — )} -------- <4-32) 0(1+w)(St)d w D 2 Ta - Tpi 1 4x 4w qw7caca = II; {'IT ' 0(l+w)(St)d 4w D(l+w)(St)d x w ( 0(l+w)(St)d ) EXP ( ' w B ) } ----- (4-33) -29- CHAPTER V EXPEREMENTAL Experimentalggystem A diagram of the experimental system is shown in Figure 5.1. The system consisted of three separately controlled systems; particle feed and recovery system, air metering and flow system, and heat transfer system. The wall of the heat exchanger was held at the uniform temperature for the experimental portion of this investigation. 1. Particle Feed and Recovegy System A stainless-steel powder collector I was used as a source of product in the experiments. This container has approximate dimensions of a 5 ft. height and a diameter ranging from 0.5 ft. at bottom to 3 ft. at the top. An agitator which turned around a vertical axis and a 2-in. diameter auger were added to the container. The auger was turned by a variable speed motor which allowed the solids feed rate to be varied from 1.5 to 9 lbs/min. The particles were carried by air through the tube to the separator and collected in the container II. The particle feed rate was measured at the immediate outlet of the auger before introducing the air to the tube. In order to check for influence of air flow on particle feed rate, the particles collected in container II were weighed after each experiment. The particle feed rate measured by both methods were in agreement that indications of air flow did not influence feed rate. “\ “‘ HH nocmmucoo m “ \ X X 3. d masm N "w non-m3 \“u u“ = “I“ . “:w 0 mop-5m “u"\ a. noumz \u u“ "5.. 3"“ u _ s; uoamumATm \n u“ _ \ _ “ .u-Itu-uux \ u n“ _ _ \ _\ _ h.“ “I“ “I“ . \ .-\ I“ e G c. \\\ \\\\\\\\\\\\\\\\\\\\\\\‘ Q.‘ E-\\\'?' g n\\\\\\ \\\\\\\\\\\\\ s\\ \\\§§§\\\\‘\\\§\\\\\\\\\\\s\ .\ ‘\\. Houoaocoz onsuua nouoom “-\..~“-‘§§h“~\\~\.§‘~“§~.“A ‘\\. “‘§..§.~‘-‘.§..§‘.‘\\n | "Moon” v .s\\\\§\§§\§|§n~h~\\\\~\\\\§\‘\\\\\\\\\\\\.\\\\\\\\ JaSusqoxa mean Husuco> o>~o> u. .41 0...“. __ pow=< 1: 1| acuoz mooam ofinmmum> " +|l poumumw< _ H Hocwmuaoo Honcho Hmucoamuomxm H.m muawfim _ 31 - 2. Air Meteripg and Flow System Air was drawn from the room by the fan connected to the inlet of conveying tube. The air flow rate was controlled by an adjustable valve located at the outlet of the fan and was measured using a venturi tube and U-tube manometer. A 1500-watt resistance heater was placed in the air supply tube upstream from the location of product injection. The aluminum tube with 2-in. diameter (o.d.) was used in this investigation. The conveying tube length fromtfim fan to separator was approximately 30 ft. The whole conveying line was insulated by fiberglas with a 2-in. thickness. The properties of air were obtained from "Mechanical Engineering Handbook" by Baumeister (1958). 3. Heat Transfer System The heat transfer system consisted of a shell-and—tube heat exchanger and a hot water source. The experimental heat exchanger was 18-8 (chrome-nickel) stainless-steel. The hot water from the source was circulated by a water pump through the annular space between shell and tube and returned to the source. The flow rate of water was determined by introducing the returned water from the heat exchanger to a bucket which was then weighed. The heat exchanger was arranged for co-current flow in this investigation and was insulated with 2-in. fiberglas, also. Before any solids were run through the heat exchanger, many experiments were conducted to determine the characterics of the exper- 2hnental heat exchanger. According to Eckert (1963), the uniform wall temperature is defined by conditions when the heat transfer coefficient - 32 - of one side approaches infinity compared to the Opposite side. Since uniform wall temperature was assumed in this investigation, heat transfer coefficients on the water side had to be much higher than on the mixture side. In order to maintain a high heat transfer coefficient of water side, the water flow rate was fixed at 3460 lbs/hr corresponding to a Reynolds number of 1.23 x 104. Hsu (1963) suggested an equation to evaluate the heat transfer coeffici nt for the forced convection in turbu- lent flow inside annular space; h 0 0 (Nu)w = I e = 0.02 (Re)2°8 (Pr)°°33 (5%) ------------- (5-1) W With Reynolds number at 1.23 x 104, heat transfer coefficient of water side was calculated to be 312 Btu/hr-ft2-'F. The heat transfer coefficients on the air side for Reynolds number of 4.7, 5.6, 6.4, 7.3, and 9.5 x 104 were experimentally determined to be 11.5, 13.6, 14.9, 16.7, and 20.0 Btu/hr-ft2-'F, respectively. The detailed procedures for calculating air side heat transfer coefficients will be presented in Chapter VI. Comparing the heat transfer coefficient of water side with those of the air side indicates that the former was much higher than the latter. This result confirms the assumption of uniform wall temperature. Kreith (1966) suggested an equation to evaluate the heat transfer coefficient of air flow passing through a duct with uniform wall temperature. T n (sc)a (Pr) = 0.02 (Re);0°2 cfm) ------------------ (5-2) W UH where: n 0.575 for gas heating n 0.15 for gas cooling - 33 _ In case of the entrance region, the heat transfer coefficient obtained from equation (5-2) can be modified as: hea = ha (1 + 6D/L) ------------------------------------- (5-3) for D/L > 20 With the previous Reynolds numbers of the air side, heat transfer coefficients calculated from equation (5-2) and (5-3) were compared with the previous experimental results and are presented in Figure 5.2. Since acceptable agreement was observed, these results support the assumption of uniform wall temperature for the experimental set-up in this investigation. The characteristics of the experimental heat exchanger are listed in Table 5.1. Temperature Measurement According to Juveland _£‘_l. (1964) and Zarbrodsky (1966), there are diverse opinions regarding temperature measured by unshield thermocouples in a gas-solids mixture system. Other researchers assumed the unshield thermocouples measured some mean temperature between the temperature of the air and solids. Ciborowski and Roszak (1966) indicated that bare thermocouples measured the particles temperatures. It is difficult to decide which of the three opinions are correct. It is obvious that when a particle at a given temperature is submerged in a fluid at another temperature, the temperature of both phases must come to equilibrium after certain period of time or distance. If the temperatures of both phases attain equilibrium, the bare thermo- couples measure the unique temperature -- the mixture temperature. Nusselt Number of Air - (haD/ua) 300 250 200 150 100 - 34 _ Calculated from Kreith Proposed Eq. 0 Experiments 1 Res ul ts t._/\, l I l 1 1 L_J 4 l 3 4 5 6 7 8 9 10x10 Reynolds Number Figure 5.2 Experimental Nusselt number of air compared with Kreith proposed equation for constant wall temperature. 35 :um\m.1NDM1H£ Nmooo.o :um\moINuMuH£ omooo.o houumuu£\=um ¢.m mo- umnus\aum Nam N «0- x mm.- H;\QH coon um Nomno.o Now mommmo.o mum mnawao.o um mmmm.o mum ¢¢m0.~ mum mmom.~ um u um noma.o um ~moo.o um mmoma.o Howcmsuxm um .oocmumamop Hams 03:9 3 m .mocmummmmu memo umumz M .Haws menu mo muw>wuunucou HmEuosa 3: .omwm nouns mo uaomowwwmoo powmcowu Doom memo noum3 mo amass: mvfiocmmm mama Beam nouns m o .uouoamam ucoam>wnvm momma nuances mo mono coHuoom mmouu m .onsu Macaw mo mono cofluuom mmouo “Na .Hfiozm mo Handsome umccH oH< .onsu mo mono mummpsm House HH< .onsu mo mono commune noccH A .onsu mo :uwaog can .wnsu mo umumemwo nouso n .mmmcxuwnu AHmB man .onnu mo Handsome umccH ummm mo momumfiuouomumso H.m manna - 36 - This mixture temperature was employed to determine heat transfer coefficients in this investigation. The thermocouple locations are shown in Figure 5.3. Temper- ature measurements were conducted at either entrance or exit positions of each phase using copper-constantan thermocouples and a Honeywell lZ-point recording potentiometer. Temperafures of each thermocouple were automatically recorded every 60 seconds. For the case of equal inlet temperatures, the temperatures which were measured at locations 1, 2, and 3 were equal and were assumed to be the inlet conditions. For the other case, powder and air were held at different temperatures. The exposed thermocouple at location 3 was assumed to measure the inlet temperature of air. The particle inlet temperature was calculated from the initial temperatures of air and powder which were measured at locations 1 and 2, respectively based on enthalpy balance under the adiabatic conditions. The equation for particle inlet temperature is: Vapaca = +——____ - ---------------------------- - Tpi T2 v p 0 (T1 T3) (5 4) P P P The inlet temperature of mixture was obtained by: npacaTfi pr pp T2 T , = ------------------------------- (5-5) ml p C+ V PpC Va 8 a pp p Since the temperature profile within the inner tube of the heat exchanger was not plug-like, the outlet temperatures were measured at three different locations: 1/16, 4/16, and 15/16 in from the inner wall. The temperature of wall was assumed to be that of water within the annular space. From the investigation of Heldman t 1. (1969), the - 37 - equilibration distance for non-fat dry milk was approximately 4 ft. from the particle feed position. To be sure that the equilibration temperature was being measured, two thermocouples were located far down stream -- 7 ft. from the exit of heat exchanger. Due to the centrifugal force, particles tend to concentrate at the outside curvature as it moves through an elbow. In order to obtain the uniform distribution of particles within the heat exchanger, 3 particle redistributor was built at the entrance position of heat exchanger as indicated in Figure 4. The particle redistributor was a ring with l/8-in. thickness. Before the heat exchanger was connected to the conveying tube, a plexi-glass tube was connected with the conveying tube at the same location as the exchanger in order to observe the effectiveness of the ring. Based on observations at the transparent plexi-glass tube, it was found that the ring provided adequate distribu- tion of the particles. Experimental Procedures There were two types of experiments conducted in this investiga- tion. One type was with equal inlet temperature of air and particles. The second type Was conducted with the particles and air at different temperatures. For the latter case, the inlet air temperature was varied. In the case of equal inlet temperatures, non-fat dry milk was exposed to the room air for 24 hours in order to obtain the uniform temperature. For the case of different inlet temperature, hot air from the resistance heater was utilized. -38- \ J), ;, - N 4 9 water ‘0 0 o O outlet—5112: 567 T 10 room temperature 0 8 - mixture to q separator powder feeding particle redistributor hot water ."—" inlet . . . O 2 3 I 313 inletr ’ I —_‘T 6" |‘—— Figure 5.3 Location of thermocouples - 39 - Uniform wall temperature was obtained by introducing cold running water into the hot water source which was heated by steam. The hot water was then circulated through the annular space and returned to the source until the water temperature attained about 180' F. The water flow rate was fixed at 3460 lbs/hr. The temperature difference between inlet and outlet water was no more than 2' F. Solids introduced into the system required additional time for establishing steady-state conditions. Gas-solids stream temperatures were observed for steady values, which normally started 10 minutes after feeding of solids began. Data which were taken after reaching steady- state, were used to calculate heat transfer coefficients. Powder which was conveyed from container I, through the heat exchanger to the separator was held in container II for 24 hours. Before running the next test, powder was manually moved back to container 1. Because of the 24 hour exposure to the ambient air, the temperature of powder was equilibrated to that of air. Product Characteristics Non-fat dry milk was used in all experiments conducted. Most of product characteristics were taken from the information available. The mean particle diameter was assumed to be 60 micron based on results reported by Hayashi _£ a}, (1967). A particle density of 1.46 was used based on data reported by Hall and Hedrick (1966) and verified by Chen (1969). A specific heat of 0.36 Btu/lb-‘F was used in heat transfer calculations and prediction of equations. This value was - 40 - predicted based on product composition and was verified by experimental determination in a Differential Thermal Analyzer. However, the experimen- tal results showed that the specific heat of non-fat dry milk increased rapidly when the temperature was above 130' F. The maximum value of 0.6 Btu/lb-°F occurred at 170° F and higher temperatures resulted in decreased specific heat. Below 130° F the specific heat was independent of temperature and 0.36 Btu/lb-°F was used. The particle thermal conductivity reported by Chen (1969) was 0.26 Btu/hr-ft-°F at 3.5% moisture content and 100° F. The particle heat transfer area was computed by a method proposed by Zenz and Othmer (1960) as: where pp and ptp are weight density per unit volume of fluidized powder in air and true particle density, respectively. The fluidized powder density can be written as: L. Pp = G ------------------------------------------- (5-7) -€°Joc’ ._2 + pa For the case of dilute transport, Ga/pa is much greater than GP/pp. The term of Gp/pp , therefore, can be neglected. The particle heat transfer area can be simplified to: 6paG A T—2 --------------------------------------------- (5-8) p G P P a According to this expression, the particle heat transfer area can be estimated by knowing particle size and loading ratio. - 41 _ Dry milk is highly sensitive to moisture as indicated by Heldman .g£._l. (1965). The experimental powder was determined to be 3.5% moisture content by a standard "Toluene Moisture Test", as indicated by Triebold _£.fll° (1963). In order to check whether mass transfer occurred during the experiments conducted, tests were conducted as a part of this investigation. The results indicated that there was no detectable change of powder moisture content. - 42 _ CHAPTER VI RESULTS AND DISCUSSIONS The experimental results of this investigation can be placed in two categories; heat transfer results and temperature histories. The experimental data are summarized in Appendix D. Heat Transfer Results According to Eckert (1963) and Kreith (1966), heat transfer rate in a shell-and-tube heat exchanger can be defined by: qw = UnDLATm -------------------------------------------- (6-1) where ATm is the logarithmic mean temperature difference (LMTD) and can be expressed as: ATmi - ATmo AT = m AT 1n( mi) ATmo where AT.=T.'T m1 m1 w ATmo g Tmo - Tw Heat transfer rate (qw) can also be determined by the enthalpy increase of the gas-solids mixture, qw = (Gaca+ cpcpxtrmo - Tmi) ---------------------------- <6-2) _ 43 - By combining equation (6-1) and (6-2) the following equation is obtained: = (GaCa+GpCp)(Tmo-Tmi) fiDLATm u ------------------------------- (6-3) 0n the right hand side of equation (6-3), the parameters can be either measured or obtained from the information available as indicated in F, I Chapter V. The overall heat transfer coefficient U, therefore, can i i be evaluated. The overall heat transfer coefficient (U) is also defined i i by: i i 11 1 1 i —=—+—+— .................................... - 1 U h k h (6 4) i w t m L Equation (6-4) can be written in another form: = + ....................................... .. R0 RW Rt + Rm (6 4) where R0: l/U, overall resistance Rw: l/hw, water side resistance Rt: b/kt’ tube wall resistance Rm: 1/hm, mixture side resistance For 18-8 (chrome-nickel) stainless steel, thermal conductivity (kt) is equal to 9.4 Btu/hr-ft-°F as given by Eckert (1963). The wall thickness (b) was 1/16 in. resulting in a tube wall resistance (Rt) of 0.00056 hr-ft2-°F/Btu. The heat transfer coefficient on the water side was evaluated by equation (5-1) as 3l2 Btu/hr-ft2-°F. The water side resistance (Rw) was then determined to be 0.00032 hr-ft2-°F/Btu. By knowing Rt’ Rw’ and U from the experimental results, the mixture side resistance was evaluated from equation (6-5) which can be rearranged as: R = a - 0.00088 --------------------------------------- (6-6) m 0 - 44 - From equation (6-6), heat transfer coefficients of the mixture side (hm) were computed and hence the mixture Nusselt number, hmD (Nu)m = .12— a The mixture Nusselt numbers calculated by these procedures are presented in Appendix D and E and are plotted on log paper in Figures (6.1) to (6.3). Figures (6.1) and (6.2) give the results of equal inlet temper- atures (EIT) and the results in Figure (6.3) were obtained with different inlet temperatures (DIT). In these figures, mixture Nusselt numbers are plotted versus either mixture Reynolds number or the convective capacity parameter (CCP). The slopes were obtained by a least square fitting procedure on a Mathatron 4280 computer. The slapes of mixture Nusselt number versus Reynolds number for constant convective capacity parameters of 1.0, 1.54, and 1.84 were obtained to be 0.8, 0.62, and 0.59, respectively, and are presented in Figure (6.1). For the air stream alone( convective capacity parameter equal to unity) the slope of 0.8 is the same as equation (5-2) as proposed by Kreith (1966). For the case of uniform wall temperature, Farbar 3E 21. (1957) and Danziger/(1963) indicated that the slopes of mixture Nusselt number versus mixture Reynolds number in the fully developed region were 0.6 and 0.66 respectively. According to Depew _t'al. (1963), the gas solids flow is fully developed if there is a constant pressure gradient along the axial direction. At the entrance region studied in this investigation, the average slope was determined to be 0.61 which is between the results of Farbar t 1. (1957) and Danziger (1963). The average slope was computed as the arithmetic mean of 0.62 and 0.59. By comparing the Mixture Nusselt Number (hmD/ka) - 45 - 400 r. 300- 250- 200L- 150?- 100‘ A 1 I L J 1 l L L J 1 3 4 5 6 7 8 9 10 Reynolds Number (DVa/ua) x 104 Figure 6.1 Mixture Nusselt number vs. Reynolds number for various convective capacity parameters. - 46 - results of this investigation with the results of Farbar 35 El (1957) and Danziger (1963), good agreement is indicated. From equations (5-2) and (5-3), proposed by Kreith (1966), it is obvious that heat transfer rate for the air stream at either the entrance of the fully developed region depends on the 0.8 power of Reynolds number. The same relationship was obtained in this investigation. Heat transfer rates of the gas-solids system depends on the 0.6 to 0.66 for both entrance and fully developed regions. The other relationships between mixture Nusselt number and convective capacity parameter were determined. For the case of equal inlet temper- atures, the slopes of mixture Nusselt numbers versus convective capacity parameter for constant Reynolds numbers of 4.7, 5.6, and 7.3 x 104 were found to be 0.79, 0.73, and 0.72, respectively. Figure 6.2 illustrates those results. For the second case, the inlet temperatures of particles and air were held at the different temperatures. In order to investigate whether there was a difference in heat transfer rate between equal and different inlet temperatures, the mixture Nusselt number was plotted versus the convective capacity parameter. The slopes of mixture Nusselt numbers versus convective capacity parameter for constant Reynolds numbers of 4.7 and 5.6 x 104 were determined as 0.72 and 0.73, respectively as illustrated in Figure 6.3. Comparing the results of two cases indicates that there was no significant difference in heat transfer rate between equal and different inlet temperatures. The experimental results of both cases, therefore, were combined in order to establish the general correlation. If the combined data of mixture Nusselt number tunnber are divided by Reynolds number to the 0.61 power [(Nu)m/(Re)£°61 ] Mixture Nusselt Number (hmD/ua) 400 - 300 250 200 150 - 47 - 1.0 1.5 2.0 2.5 3.0 4.0 5.0 G C Convective Capacity Parameter (l +-E£E£) a a Figure 6.2 Mixture Nusselt number vs. convective capacity parameter for various Reynolds numbers with equal inlet temperatures. Mixture Nusselt Number (hmD/ua) 400 300 250 200 150 100 \x \Q (0+ IC). ’ v F ‘10 Q a \ ® 4- “3‘ __ i X 0 1— O a "a ,'X ‘L 9"“ 3 —9\,0 Q l J l l J 1.0 1.5 2.0 2.5 3.0 4.0 G C Convective Capacity Parameter (1 + CECE) a a Figure 6.3 Mixture Nusselt number vs. convective capacity parameter for various Reynolds numbers with different inlet temperatures. - 49 - and plotted versus the convective capacity parameter, it reveals a 0.73 power relationship as illustrated in Figure 6.4. The value of the vertical intercept for the convective capacity parameter of unity was found to be 0.17. The standard deviation was calculated to be 17%. For the same uniform wall temperature system, a considerably different re- sult was observed between the entrance region of this investigation and the fully developed region in the research by Farbar _£ 31. (1957), Tien _£__l. (1962) and Jepson £3 al. (1963). Farbar _£‘_l. (1957) showed that there was no increase of heat transfer rate at a loading ratio of less than one. Tien £5 al. (1962) and Jepson _t al. (1963) indicated that due to the inertia, solid particles could conceivably reduce the scale of turbulence in the air when the loading ratio was less than one, also. The results of this investigation illustrated that any addition of solid particles increases the heat transfer rate from wall to the mixture. This phenomena may be due to the addition of particles at the entrance region causing the change in air flow characteristics. After the addition of particles, the air stream must accelerate particles to the constant velocity as well as distri- l>ute particles within air stream according to the momentum balance. Tfliis change of the air flow characteristics may continue from the particle entrance location to where the fully developed flow is attained arid consequently increase the scale of turbulence in the entrance region. vae heat transfer rate could be increased, also. 0.61 a (Nu)m/ (Re) 0.50 0.40 0.35 0.30 0.25 0.20 -50- 0.73 0 experimental data correlated line 0.15s- 0 61 G C 0.73 = . ' + °. (Nu)m 0 l7 (Re)a (1 Gaca) (i7/) 0. 1 1 J 1 1 1 1.0 1.5 2.0 2.5 3.0 4.0 G C Convective Capacity Parameter (1 + CECE) a a Figure 6.4 The combined Nusselt number versus convective capacity parameter. - 51 - From the literature review, most investigators correlated mixture Nusselt number in terms of Reynolds number (Re)a and loading ratio (Gp/Ga)' The exception is the Babcock & Wilcox Co. (1959) work which correlated the mixture Nusselt number in terms of Reynolds number and the convective capacity parameter. Tien's (1960) theoretical analysis showed that mixture Nusselt number was a function of Reynolds number and convective capacity parameter instead of loading ratio. He also indicated that the increase of heat transfer rate by addition of particles to an air stream was due to the high volumetric specific heat of particles. From Tien's (1960) investigation, it was illustrated that the different heat transfer rates would be caused by different materials which possess different specific heats. If the loading ratio is used to correlate the experimental results, the correlation may be valid for a specific material only. In order to generalize the correlation, heat transfer results were correlated in terms of mixture Reynolds number and convective capacity parameter in this investigation. The correlation is: G C 0.73 G C ) (i7%) ---------------- (6-7) aa (Nu)m = 0.17(Re);)°61 (l + Equation (6-7) is valid for convective capacity parameter greater one land for the entrance region of a constant wall temperature system. Temperature Histories Due to the existing disagreement regarding temperature measure- metit in gas-solids systems, the measured temperature profiles at exit POEBitions of the heat exchanger cannot be assigned to any one phase. Th6! only unique temperature which can be obtained is the mixture temper- _ 52 - ature of both phases at a downstream location. In order to avoid the controversy, this mixture temperature was used to calculate heat transfer coefficients. The measured temperatures are presented in Appendix D I and E. With the aid of equation (6-7), the temperature histories of gas-solids system can be predicted from the derived equations of Chapter 4. For the case of equal inlet temperatures, the temperatures of air and particles can be predicted from equation (4-17) or (4-18) respectively. The mixture temperature can be predicted by the computed temperatures of air and particles according to equation (4-5), = VapaCaTa + vpppCpr _____________________________ (4_5) + m Vapaca VpppCp T The computed temperatures are presented in Appendix F. Because mixture temperature is the only property which can be measured accurately, the mixture temperatures which were predicted at the exit Position of the 4-ft heat exchanger were compared with those from the experiments. The comparison are presented in Figure 6.5 and 6.6 where good agreement is indicated. As indicated previously, heat transfer rate is a function of the convective capacity parameter rather that the loading ratio. However, the loading ratio can be used in place of the convective capacity parameter if a specific material is considered. In order to illustrate how the degree of loading of particles influences the temperatures of both phases, the loading ratio will give a more concise explanation than the convective capacity parameter. In Figure 6.5 and 6.6, the temperature histories, therefore, are plotted versus the loading ratio. For the case of different inlet temperatures, - 53 - the outlet temperatures of air and particles can be predicted from equations (4-15) and (4-16) respectively. The mixture outlet tempera- ture can be predicted by the computed temperatures of air and particles according to equation (4-5). Equations (4-15) and (4-16) illustrate that the dhmensionless temperature ratios of air and particles are in terms of (Tpi - Tai)/(Tpi - Tw)' It is impossible to plot the results of the different inlet temperature case since (Tpi - Tai)/(Tpi - Tw) was not controlled as a constant value in the experiments. For this reason, the predicted temperatures of mixture and both phases are presented in Table 6.1 instead of plotting. By comparing the predicted and measured temperatures of mixture in each individual experiment, good agreement is obvious. Since the temperatures of air and particles cannot be measured directly, there is no direct method to verify the derived equations. Fortunately, the mixture temperature of air and particles can be obtained experimentally or predicted theoretically. The predicted mixture temperature comes from the computed temperatures of air and particles. If the measured and predicted mixture temperatures are in agreement, the predicted air and particle temperatures can be assumed to be the true temperatures of both phases. The derived equations, there- fore, can be verified by this indirect method. From previous comparisons of the measured and predicted temperatures, the derived equations from (4-15) to (4-18) provided a good prediction of the air and particle tempera tures . 54- numaEmu .«oH x vmuoflkua msu sums o.m u mAwmv you new one .musuxae .mmaoauuma mo mmusum wusuxwa mo mopsumumaamu umauso omuswmms wsu wawumaaou m.c muswwm m a A 0\ 0V oHumm wcawmoa o; as we so as m5 10.0 m5 «.0 no 1. _ a _ _ _ a _ _ _ so an. 1 an. m 3 m u m m.o B 1 B 3 .— a - .a so 3 s n H 1 B 0.0 3 a - an. no 3| 0 B I H mm «HHQ co 3 1IAWI1, “W1 Em .musuxwaxlli mm .mm ofiuuma fl w.o 338363 33ow consumes o mmusumumaamu vmumaaono o.o o.H s ( 9 ‘me ‘d9) sarnnexadwal ssaIuorsuamra 55 . OH x n.¢ u mAwmv now Ham was .wusuxwa .mmaowuuma mo mmusumumaamu vouowomwa wsu Lugs musuxfls mo mousumumaEmu umfiuso umusmmwe mau wswumaaoo 0.0 muswwm A00\000 00000 wca0moa 0.a 0.0 0.0 h.0 0.0 m.0 0.0 0.0 ~.0 3.0 _ _ _ _ fi _ — fl a _ 3a - as 1 00 0 1 3H - e 3a - He 1 50 3a - as 3H - as 00 mflllld1.u a - e 111 10. O 0111111 E0 .9533": am .maowuuma salnnexadmal ssaIuorsuamrq OHDU QR UQEUU wHSUKHB kan—wflwa mmuaumumaamu omuownmua m.o m.o - 56 - Table 6.1 Comparison of the predicted and measured mixture temperatures (Different Inlet Temperature) Calculated Measured Loading (°F) _ (°F) Tw Tai Tpi Ratio C.C.P. Tmo Tmo Re 185.8 140.5 115.7 0.31 1.47 145.8 146.5 5.6 x 10 177.0 141.5 117.5 0.36 1.54 144.6 145.5 5.6 178.0 135.0 114.0 0.41 1.62 139.8 140.3 5.6 181.9 130.9 112.3 0.56 1.84 136.1 137.0 5.6 176.8 133.0 103.3 0.65 1.91 133.0 133.8 5.6 186.8 127.0 105.9 0.8 2.2 133.1 133.5 5.6 197.3 130.0 108.7 0.82 2.23 137.3 140.0 5.6 183.5 127.0 111.8 1.04 2.56 133.5 134.0 5.6 180.8 137.4 126.7 0.36 1.78 145.7 146.4 4.7 183.3 139.5 120.5 0.39 1.82 147.1 146.8 4.7 179.3 138.1 113.8 0.47 1.85 142.4 141.6 4.7 184.0 140.0 113.7 0.53 1.92 142.3 141.8 4.7 179.0 130.8 116.0 0.56 1.84 138.9 141.0 4.7 184.3 133.5 111.5 0.67 2.0 139.5 139.5 4.7 182.5 129.0 113.5 0.82 2.23 137.1 136.8 4.7 184.0 129.0 109.7 0.93 2.4 134.3 136.0 4.7 - 57 _ A technique for measuring the temperatures of air and particles has not been developed. The temperature profiles were measured by four bare thermocouples at the exit location of heat exchanger in an attempt to obtain valid comparisons. According to Farbar gt 31. (1957), the volumetric ratio of solid to air stream in gas-solids system is so small that the bare thermocouples which are exposed to the mixture stream measure the air temperature only. This assumption seems plausible at low loading ratio. By assuming the measured temperature profile is the air temperature profile, the outlet temperature of air can be calculated from the measured profile by the method preposed by Henderson (1955). This average outlet temperature was determined by dividing the conduit into a number of small areas, and finding the average over the total area. A system for doing this is shown in Figure 6.7. The method of calculation can be expressed as: = l. ........................... - Tao S (T851+T382+T5S3+T484) (6 9) __1_ 2 2 2 2 2 2 2 R ......................... (6-10) The measured outlet temperatures of air from the outlet temperature profiles are presented in Appendix F and compared with those predicted from the derived equations (4-17) and (4-18). In Figure 6.8 and 6.9, the predicted and measured temperatures are plotted versus the loading ratio. The comparisons illustrate an interesting result. For a loading ratio of less than 0.56, the measured outlet temperatures of air are exactly as same as those predicted from the derived equation. At a loading ratio of 0.82, the measured outlet temperatures of air are - 5g - R = 15/16 in. R1 = 13/16 in. R2 = 7/16 in. Figure 6.7 Thermocouple locations at the exit position with its represented areas. m . 0H x 0.0 u Awmv you Ham 0cm .wusuxfle .mmaowuuma mo mwusumuwmeuu uwfiuso wwuuwwwua 0 wsu sues enqu0E was mwaoauuma mo mousumuwmaou uwauso vwnsmmme msu weaummeoo 0.0 wusmam a Amo\ 00 oaumm 0000000 0.0 0.0 0.0 5.0 0.0 0.0 0.0 0.0 N.0 0.0 0 _ _ a _ _ a 0 _ _ a 3e - .0. 3 m H u H 3 a H 1 .H 1 3 E 1 H - H _ 3 a M... a - a. - milldfi.1 _ H 1 a ( X 111‘ M O 0111111111111IWI111 o 0 011111 0 .393an 3503383 umauao 00539: X 0 mwusumquEwu wusuxwa wwusmmme mousuwumaawu Umuuwkua 0.0 m.0 a m a u S T. 0 U 0.0 n S 3 Tu a m d a 3.0 u 14 n 1 3 S 0.0 an. 9 m e 0.0 m1 0.0 60 - m .00H x 5.0 u Awmv now “Hm 0cm .musuxwe .mwaowuuma mo mouaumumasmu umfiuso Umuoflnmua mnu £003 musum 1uwQEmu ousuxwe wmusmmme mzu 0cm mounumquEmu umauso emusmmms msu wcfiumaeou 0.0 muswam Amw\auv oHumm wcfivwoq 3H as 0 3 m u m H 1 H 3 0 H 1 H 1 50 3 E I H 1 a 3 a 0. - .0 1 a0 MIIIIMI 1 H 1 H mm 1yMl1 11 I119|| O 80 Jun 0111 1|I~WII 00 .oHoHuuma XI musumuwaamu 9.0390 00.3038 X 3330083 muauxfie 00.30me 0 mmuaumquEmu vmuoakuu 1111 5.0 0.0 0.0 0.0 (99 ‘me ‘de) saznneladmal ssaIuoisuamrq - 61 - similar to the predicted or measured mixture temperatures. When the loading ratio is increased to unity, the measured outlet temperatures are close to the particle temperature as predicted from the derived equation (4-17). According to the assumption in the theoretical development, there is no direct heat transfer between particles and tube wall in the case of arbitrary wall temperatures. Particles can only be heated by obtaining heat energy from air. The temperature of the particles, therefore, never reaches that of air as long as the temper- ature gradient exists between mixture and tube wall. However, the measured outlet temperatures of air at a loading ratio of one is lower than the predicted and measured mixture temperatures and close to the predicted particle temperature. The temperature reading of bare thermo- couples at a loading ratio of one, therefore, did not measure the air temperature, but the particle temperature. These comparisons indicate that all three controversial opinions are reasonable depending on the loading ratio considered. Since only four thermocouples were used to establish the temperature profiles and the loading ratio was limited within the range from zero to unity, further study is necessary in order to completely explain the reason for the influence of loading ratio on bare thermocouple measurement. - 62 - CHAPTER VII ANALYSIS The following analysis for the cooling systems of spray-dried food products will be based on the previous experimental Nusselt numbers which were obtained during a heating process. According to equation (5-2), proposed by Kreith (1966), heating and cooling do not follow the same correlation of Nusselt number. The deviation due to using the heating correlation instead of the cooling one is, however, sufficiently small. For example, when air and wall temperatures are 120 and 50° F respectively, the deviation of Nusselt number is less than 5% when comparing heating and cooling correlations of equation(5-2). The types of cooling systems. used for cooling spray-dried food products will vary considerably depending on facilities available. In most cases, the cooling is accomplished by mixing the dry product with room temperature or cool air. In the dry milk plant, powder leaves the drier at approximate 120° F as indicated by Farrall _5 a1. (1968) and 600 pounds powder per 15,000 cubic foot air per hour are conveyed through a tube to the separators ((Hedrick (1969)). This loading rate is equivalent to the loading ratio of 0.56. If the con- veying tube is exposed to the room air and heat transfer of mixture to the surrounding depends on natural circulation of the ambient air around timeconveying tube, the heat transfer rate due to natural circulation is t 31. (1969). After the initial Very low as indicated by Heldman Ifxaur feet of conveying tube, the mixture temperature was reduced by only 43'; of ambie COUW In 1 air C851 air sin is Ce - 63 - 4% of the initial temperature difference between the mixture and the ambient air. This is the obvious reason that dry milk plants use conveying tube lengths of more than 100 feet in order to cool the heated powder. The natural circulation of air, therefore, can be approximated by adiabatic conditions for short sections of conveying tube. There are two types of heat transfer systems to be analyzed. In the first case, heated powder mixes with room temperature or cool air and the mixture is conveyed at the adiabatic conditions. The second case describes heated powder mixing with room temperature air or cool air and the mixture is conveyed through a shell-and-tube heat exchanger similar to the one used in this investigation. A uniform wall temperature is assumed. Both systems have the following characteristics: loading ratio, Gp/Ga = 0.56 Reynolds number, (Re)a = 5.6 x 104 powder inlet temperature, Tpi = 120° F room air temperature 80° F cool air temperature 50° F water temperature, Tw ' 50° F Using this information, temperatures of air and powder can be predicted. IFor the adiabatic conditions, air and particle temperatures can be calculated by the equations proposed by Heldman gt a1. (1969), :1: -i%; { l - Exp [ -A(St)d(l+1/w)x ] } ------- (7-1) - 64 _ 7f“??? = T113 { 1 - Exp 1 -A(St)d(1+1/W)X J } ....... ai pi (7-2) For the case of uniform wall temperature, the temperatures of both phases can be calculated from equations (4-15) and (4-16). The calculated temperature histories are plotted versus axial distance and are pre- sented in Figure 7.1. The results (Figure 7.1) illustrate how the particle and air temper- atures vary with the axial distance and the temperatures of each phase at the exit position of a 10 ft. long conveying tube. For the adiabatic conditions, heated powder at 120° F was mixed with air at 80 or 50° F. The equilibrium temperatures were calculated from equations (7-1) and (7-2) and were found to be 98 and 82° F respectively. For the case of uniform wall temperature, the particle and air temperatures at the exit of a 10 ft. heat exchanger were predicted as 66 and 74° F for particles and 64.5 and 72.4° F for air from equations (4-15) and (4-16). For the adiabatic conditions, the heat transfer potential is the temperature difference between particles and air. After the temperature of both phases comes to the equilibrium,the heat transfer potential no longer exists. The temperatures of both phases remain at the equilibrium temperature. For the case of uniform wall temper— ature, two heat transfer potentials exist. The first is the temper- ature difference between particles and air. The second is the temper- ature gradient between mixture and tube wall. Each temperature poten- tial varies with the axial distance. Theoretically, the distance for the temperatures of air and particles to come to equilibrium is infinity for the adiabatic condition. In the actual situation, the temperature 65 A.000 00000000 Hmax< was”. mamas—mu .3 m 03 353 mu wusumuomemu mHoHuumm commasonu 111111111 11. wusumumaamu 1111 111111 acaumuflisg 0333330 1 I, IIIIIII J I” I ’I I I I, I I I ’II’ / 3033500 030.033. III III III I // 1.1 / III: // I’ll / I IIe ’5 11111111111111 1 1111111111.. 11 // X coufiflvaoo 0323.2; III! / z I. X, 3 I / o I// I/ I; all... 3 . 3, .000 x 0.0 00 “mass: ,3” meaocmmm 00m 00.0 mo oflumu mewvmofi pom musuwuuaamu 5 :03 E035. 0:0 00.32500 0:00.02; no 08393 on“. news: 620330 1303 .m> mmHHOumHS wuauwuwaama Tn muswwm on 00 om. 00 00 00H 0: Qua alnnsladmal (do) - 66 - difference between two phases is not detectable after a given distance of mixing. If the distance for the temperatures of both phases to be within 1% of their equilibrium temperature is assumed to be the equilibration distance, this distance was calculated from equations (7-1) and (7-2) to be approximately 3 ft. A value of 4 ft. was measured experimentally by Heldman §£_a1. (1969). Due to temperature lag between particles and air as indicated in the previous chapter, the temperature of particles never reaches that of air as long as the temperature difference exists between mixture and tube wall. For this reason, the characteristic temperature in the case of uniform wall temperature is not the equilibrium temperature of the adiabatic system. From examination of Figure 7.1, it is obvious that a maximum air temperature occurs during the process when heated powder mixes with room air or cool air and the mixture is then cooled by the tube wall. The location of this maximum air temperature can be obtained by differentiation of equation(4-l6) with respect to axial distance and setting equal to zero. The result is: X = Dlnz ............................ (7-3) 4(St)m 1¢(St)d(1+1/W) - Tm] where: 2 2 ¢ (St)d(1+1/w) [ (1+w)ffgi:Tw)+(1/w)(Tai'Tgi) J ¢(Sc)d 4(St2;“_# 4(852; 1 -—;_—- -'(I;W)- ] ['ITTGI— ] [(1+1/w)(Tpi-Tw).w(Tai-TW) J For the example under consideration, the location of maximum air temper- ature was found to be 1.2 ft. Equations (4-15) and (4-16) illustrate that after the air temperature attains the maximum temperature, heat -67- transfer rate between air and particles is small in comparison to that between the mixture and tube wall. This result implies that the first exponential term in equations (4-15) and (4-16) is much larger than the second exponential term at some distance downstream from the location of maximum air temperature. The equations for predicting temperature of both phases downstream from the location of maximum air temperature, therefore, can be simplified by neglecting the second exponential term in equations (4-15) and (4-16) and the new equations are obtained as; : : :w = ((S:)d ) (0 l+w s g 4 s ) pi w ( )( t)d ( 1:)“.l w - (1+w) Ta. 4(St)m X . {1 (1m) - <—"-———--) J Exp 1 - 7‘10.) 5 J j ------- (M) Tpi Tw Ta - Tw _ (St)d g T .- T - ( ”) (0(1+w)(St)d 4(St) ) pi w _ .____JE w (1+w) T 1 - Tai 4(St)m {w[(1+v)-(—E—-—T—) _ T ]Exp[- (1%,)- "‘DJ} ----- (7- 5) pi w These two equations can be employed to predict the temperatures of air and particles for the case of uniform wall temperature, since the temperature of interest is not within the first one or two feet from the location of particle feeding. From the previous analysis, it was illustrated that there are two characteristic temperatures for two different cooling systems; the equilibrium temperature for adiabatic system and the maximum air temper- ature for the uniform wall temperature case. Both characteristic temperatures can be attained very rapidly after particle feeding. At the exit position of a conveying tube with 10 ft. length, the shell- and-tube heat exchanger provides the most effective cooling result while the cool air injection is more effective than the room temperature air injection under the assumed adiabatic conditions. The convective capacity parameter is a characteristic parameter of gas-solids system during heat transfer. As indicated in the previous chapter, heat transfer rate is dependent upon the convective capacity parameter instead of loading ratio. However, the loading ratio can be utilized instead of the convective capacity parameter if only one material is considered and its specific heat is constant with respect to temperature. Table 7.1 indicates the comparison of the outlet temperature of powder at the exit position of a conveying tube with 10 ft. length for various loading ratios. This comparison was made to investigate the difference between the adiabatic and the uniform wall temperature systems when powder at 120° F is mixed with 80 or 50° F cool air under adiabatic conditions, or then conveyed through the tube with 50° F wall temperature. For the adiabatic conditions, the particle temperature can be cooled below 80° F at a loading ratio of 0.36 and with cool air injection. In the case of uniform wall temperature, the heated particles can be cooled below 80° F at any loading ratio 1>elow 1.04 and with cool air or room air conveying. This comparison illustrates that rapid cooling can be accomplished even at high loading Instio and with uniform wall temperature. In order to increase cooling reate under adiabatic condition, a low loading ratio should be employed 0!? a long conveying tube is required for natural circulation of room airu However, the system of cool air injection with cold wall temper- 69 30 .m m Ou meammm m0 .. H .musumuwQEmu um c0 0 owuumm 0000 0 0 H H e. «w on m 000 u H 0.00H ~.~0H 0.00 0.00 H coHuwvcou oflumnmwv< 0m 00 m 000 u H 0.00 0.00 0.00 0.00 H 0 coHuwvcoo oHumnm00< 3 m 000 u . H 0.00 0.00 0.00 0.05 H .QEmu H~m3 Buomwcb 3 m 000 u amH 00 m 000 u . H 0.00 0.00 0.00 0.00 H r1 .QEwu HHm3 EuomHs: sowuwocoo 00.0 00.0 00.0 00.0 owumm 0 :03 0000000 .Amov .meo«uwweoo HHm3 uamummwwv 0cm mofiuwu mswvmofi msofium> Hows: mono 0c0>m>coo .um 0H a mo scauwmoa uwxm msu um mmaowuuma mo mwusumummfimu umfiuso 03H 0.0 mHQwH -70.. ature can offer rapid cooling with a short conveying distance. The dry milk industry is concerned about the airborne contamination of finished products by Salmonelleae. Since the conveying tube for the system of cool air injection with cold wall temperature is much shorter than that of natural circulation system, the power required to overcome the pressure drop of a long conveying tube can be used to draw air through a high efficiency air filter. The dry milk industry, therefore, can obtain high air purity and the more effective cooling at comparable operating costs. Reynolds number is an additional parameter which influences the temperatures of both phases. It is obvious that Reynolds number influ- ences the retention time of particles within the conveying tube. The longer the retention time of particles within the conveying tube, the more heat energy per pound of powder transmitted. This explanation can be verified by the experimental results in Figures 6.5 and 6.6. These two figures illustrate that at the lower Reynolds number, particle temperatures are closer to the wall temperature. In order to obtain cool powder, a low Reynolds number is suggested. However, Zenz (1964) indicated that there was a minimum air velocity at which particles can be conveyed. The lowest Reynolds number, therefore, cannot be less than the minimum Reynolds number for particle conveying. The particle size affects the equilibration distance for the adiabatic condition and the location of maximum air temperature. It does not influence the equilibrium temperature and maximum air temper- ature, since the particle size determines the heat transfer area between Particles and air stream. The smaller particle size, the more heat - 71 - transfer area. The smaller particles, therefore, require shorter distance to attain the equilibrium temperature or maximum air tempera- ture in the case of adiabatic condition or uniform wall temperature, respectively. The unique parameter of particle size should be repre- sented by the combined parameter, (St)d¢, because both (St)d and fl include particle diameter (dp). Due to small particle size and small relative velocity, particle surface parameter, fl, and particle Stanton number, (St)d, are the order of magnitude of 10 and 1, respectively. The mixture Stanton number, (St)m, however, has the order of magnitude of 10-3. By comparing the order of magnitude, (St)d¢is much greater than (St)m. Based on this observation, the following relationship exists in equation (7-4). (St)d9)(1+w) 4(St)m >> ”(1”)- Equation (7-4) can then be simplified further to: ELL-.30 1 Tei'Tai 4(St)“. x Tpi-Tw = T476 i0”) ' (Tpi- 1;) i EXP [ ' T355." '13] ------------------------- (7-6) This equation clearly illustrates that particle size does not contrib- ute to the particle temperature history at locations downstream from the location of maximum air temperature. Based on the previous analysis, particle temperature history at locations downstream from the location of maximum air temperature is controlled primarily by three parameters; mixture Stanton number, (St)m, initial temperature ratio, (Tpi-Tai)/CTpi-Tw), and convective capacity ratio, w. As mentioned earlier in this chapter, the particle temperature of interest is not necessarily that at locations upstream - 72 - from the location of maximum air temperature. The temperature history at downstream locations can be illustrated by plotting equation (7-6) as illustrated in Figures 7.2, 7.3, 7.4 and 7.5. Since the parameter (St)d¢ does not influence the particle temperature history, the charts can be applied to any practical range of (St)d¢. The charts of Figures 7.2 to 7.5 show the dimensionless temperature,(Tp-Tw)/(Tpi- Tw), as a function of the axial distance parameter, x/D, for various values of w, (Tpi-Tai)/(Tpi-Tw), and (St)m. Each chart has a fixed convective capacity ratio, w. In each chart, there are three separate graphs for initial temperature ratios, (Tpi - Tai)/(Tpi - Tw) of 0, 0.5, and 1.0. Since the charts are not continuous for the values of w and (Tpi - Tai)/(Tpi - Tw)’ interpolation can be used for the first approximation. In summary, the analysis indicates that the shell-and-tube heat exhanger will provide better cooling effectiveness. It should be emphasized that the shell-and tube heat exchanger can cause the vapor condensation on the inner surface if the wall temperature is lower than the dew point temperature of air stream. The powder, therefore, may stick to the wall and hence reduce the heat transfer rate. In order to prevent the vapor condensation, inlet air temperature should be maintained several degrees lower than tube wall temperature. Since air is cooled before entering into the heat exchanger, the condensation Will occur on cooling coils before passing over the cool surface. In addition, the inlet air, even with 100% relative humidity, never attains the dew point temperature as long as the temperature of tube wall is higher than that of the inlet air. For the actual cooling design, it is - 73 - necessary to check the relative humidity of inlet air and its dew point temperature. The condensation problem, however, can be neglected if the temperature of inlet air is maintained lower than that of tube wall. - T )/(T 1 - Tw) (T G) W = 0.45 91= 1.0 5 10 Figure 7.2 _ 74 - 15 20 25 30 35 40 45 50 55 x/D Dimensionless temperature history of particles along the axial distance during pneumatic transport of spray-dried food products. 60 (Tp - Tw)/(TPi - Tw) DJJ-‘UIO‘QO .9 Ln a~ <0 23 w = 0.84 91= 1.0 5 10 Figure 7.3 - 75 - 15 2 25 30 35 40 45 50 55 60 x/D Dimensionless temperature history of particles along the axial distance during pneumatic transport of spray- dried food products. (Tp - Tw)/(TPi - Tw) 61= 0.5 - _. a- .— I . tit-1} fit _ +_ WT-.. I —.-'.-_.‘ ._.,-.. ____. I ---- 5 10 15 20 25 30 35 40 i 45 50 55 60 x/D Figure 7.4 Dimensionless temperature history of particles along the axial distance during pneumatic transport of spray- dried food products. ('1:p - Tw)/(Tpi - Tw) _ 77 _ W = 1.5 9.“ 1.0 i 5 10 Figure 7.5 15 20 25 30 35 40 45 50 55 60 x/D Dimensionless temperature history of particles along the axial distance during pneumatic transport of spray-dried food products. _ 7g - CHAPTER VIII CONCLUSIONS In a gas-solids mixture systems, mixture Nusselt number depends on 0.6 to 0.66 power of Reynolds number disregarding to entrance or fully developed region. There is no significant difference in the mixture heat transfer coefficient between equal and different inlet temperatures of air and particles in gas-solids system. The mixture Nusselt number was correlated as: G C 0.73 (Nu)m = 0.170103“ (1 + 59-53) (177.) a a This empirical equation is valid for the convective capacity parameter greater than unity and within the entrance region in the case of uniform wall temperature. Heat transfer rate as expressed by the mixture Nusselt number increases with loading ratio in the entrance region, as compared to the decrease in rate between loading ratios of 0 and l for the fully developed region. Bare thermocouples measure the air temperature when the loading ratio is below 0.56, the mixture temperature at the loading ratio of 0.82, and the particle temperature at loading ratios greater than unity. Based on the verification of the indirect method, the temperatures of air and particles are adequately predicted by equation (4-15) to (4-18) for the case of uniform wall temperature. After the air temperature attains the maximum temperature, heat transfer rate between air and particles is small in comparison to that between mixture and tube wall. Particle size only determines the location of maximum air temper- ature and does not influence the maximum air temperature itself. Based on the analysis of different cooling systems, a shell-and- tube heat exchanger should provide better cooling effectiveness at a high solid loading ratio. -80- CHAPTER IX RECOMMENDATIONS FOR FUTURE WORK Determine the mixture Nusselt numbers for linear wall temperature and constant heat flux systems and verify the derived equations. Investigate the influence of loading ratios on the bare thermo- couples reading more thoroughly. Determine the mixture Nusselt numbers with different particle sizes and find out the dependence of mixture on the particle sizes. Determine the mixture Nusselt number with different materials and verify the dependence of mixture Nusselt number on the convective capacity parameter. Measure the temperature histories along the axial direction and compare to the calculated results. Measure the scale of turbulent in the entrance region within the loading ratio of unity and check with that of fully developed region. -31- BIBLIOGRAPHY - 32 - BIBLIOGRAPHY Allen, T. 1968. Particle Size Measurement. Chapman and Hall, LTD., London. Babcock and Wilcox Co., Atomic Energy Division. 1959. Cited by Danziger, 1963. Bakker-Arkema, F. W., J. R. Rosenau, and W. H. Clifford. 1969. Measurement of Grain Surface Area and Its Effect on the Fixed and Moving Beds of Biological Products. American Society of Agricultural Engineers Paper No. 69-356. Baumeister, T. 1958. Mechanical Engineers' Handbook. McGraw-Hill Book Company, Inc. Sixth Edition. Belden, D. H. and L. S. Kassel. 1949. Pressure drops encountered in conveying particles of large diameter in vertical transfer lines. Ind. and Eng. Chem. 41-1174. Breiman, L. 1952. Theory of heat and mass transfer from a slowly moving sphere to the surrounding medium. Report No. 2F-2, Norman Bridger Lab. Calif. Inst. of Tech., Pasadena, Calif. Chen, A. C. C. 1969. Mechanism of Heat Transfer Through Organic Powder in a Packed Bed. Ph.D. Thesis. Department of Agricultural Engineering, Michigan State University. Ciborowski and Roszak. 1954. Cited by Zabrodsky, 1966. Danziger, w. J. 1963. Heat transfer to fluidized gas-solids mixtures in vertical transport. I and EC Process Design and Development. 2(4): 269-276. Davidson, J. F. and D. Harrison. 1963. Fluidized Particles. Cam- bridge, At The University Press. Depew, C. A. and L. Farbar. 1963. Heat transfer to pneumatically conveyed glass particles of fixed size. Trans. of the ASME, J. of Heat Transfer. 85C:l64-l72. Drake, R. M. 1961. Cited by 800, 1967. Eckert, E. R. G. 1963. Introduction to Heat and Mass Transfer. Translated by Joseph, F. G. McGraw-Hill Book Company, Inc., New York. V Farbar, L. and M. J. Morley. 1957. Heat transfer to flowing gas—solids mixtures in a circular tube. Inc. and Eng. Chem. 47(7):ll43-1150. - 83 _ Farbar, L. and C. A. Depew. 1963. Heat transfer effects to gas-solids mixtures using solid spherical particles of uniform size. I & EC Fundamentals. 2(2):130-135. Farrall, A. W., A. C. Chen, P. Y. Wang, A. M. Dhanak, T. I. Hedrick and D. R. Heldman. 1968a. Thermal conductivity of dry milk in a packed bed. American Society of Agricultural Engineers Paper No. 68-386, St. Joseph, Michigan. Farrall, A. W., A. C. Chen, P. Y. Wang, and D. R. Heldman. 1968b. Field performance of dry milk cooling and storage systems. American Society of Agricultural Engineers Paper No. 68-883, St. Joseph, Michigan. Hall, C. W. and T. I. Hedrick. 1966. Drying of Milk and Milk Products. The AVI Publishing Company, Inc., Westport, Connecticut. Hanrahan, F. F., R. L. Selman and B. H. Webb. 1967. Experimental equipment for cooling and packaging foam-spray-dried milk in the absence of oxygen. J. Dairy Science. 50(12):1873-1877. Hariu, O. H. and M. C. Molstod. 1949. Pressure drop in vertical tubes in transport of solid by gases. A. I. Ch. E. Journal. 41:1148. Hayashi, H., D. R. Heldman, and T. I. Hedrick. 1967. A comparison of methods for determining the particle size and size distribu- tion of non-fat dry milk. Michigan Experimental Station, Michigan State University, Quarterly Bulletin 50(1):93-99. Hedrick, T.I. 1969. Personal Communication. Heldman, D. R., C. W. Hall and T. I. Hedrick. 1965. Equilibrium moisture of dry milk at high temperature. Trans. of the ASAE. 8(4):535-54l. Heldman, D. R., P. Y. Wang, and A. C. Chen. 1969. Effectiveness of cooling systems for spray-dried food products. Institute of Food Technologists Paper No. 574. Chicago, Ill. Henderson, S. M. 1955. Agricultural Process Engineering. John Wiley & Sons, Inc. New. Chapman & Hall, LTD., London. Heywood, H. 1962. Symposium on the interaction between fluids and particles. Inst. Chem. Eng., 1. Hinkle, B. L. 1953. Acceleration of Particles and Pressure Drops Encountered in Horizontal Pneumatic Conveying. Ph.D. Thesis. Georgia Inst. of Technology. - g4 - Holman, J. P. 1968. Heat Transfer. McGraw-Hill Book Company, New York. Hsu, S. T. 1963. Engineering Heat Transfeg. Princeton, New Jersey. Jepson, G. A. and W. Smith. 1963. Heat transfer from gas to wall in a gas-solids transport line. Trans. Inst. Chem. Engrs. 41:207-211. Jones, J. H., W. G. Braun, T. E. Danbert, and H. D. Allendorf. 1966. Slip velocity of particulate solids in vertical tubes. A. I° Ch. B. Journal. 12(6):1070-1074. Juveland, A. C., H. P. Deinken and J. E. Doughert. 1964. Particle- to-gas heat transfer in fluidized bed. I & EC Fundamentals. 3(1):329. Kreith, F. 1966. Principles of Heat Transfer. International Textbook Company. Scranton, Penn. Kubnek, G. R., P. C. Alien, and W. H. Gauvin. 1968. Heat transfer to spheres in a confined plasma jet. The Canadian Journal of Chemical Engineering. 46:101-107. tha, T. P., A. W. Farrall, A. M. Dhanak, and C. M. Stine. 1966. Determination of heat transfer through powdered food products. American Society of Agricultural Engineers Paper No. 66-823. Orr, C., Jr. 1966. Particulate Technolggy. The MacMillan Company, New York. Ossen, Cited by $00, 1967. Rowe, P. N., K. T. Claton, and J. B. Lewis. 1965. Heat and mass transfer from a single sphere in an extensive flowing fluid. Trans. Inst. Chem. Engrs. (London) 43:T14. Russ and Culgan. 1950. Cited by Zenz and Othmer. Schillar and Nauman. 1933. Cited by $00, 1967. Sissom, L. E. and T. W. Jackson. 1966. Temperature distribution of solids and fluid in fluid to particle heat exchanger. The American Society of Mechanical Engineers Paper No. 65-HT-l7. Sissom, L. E. and T. W. Jackson. 1967. Heat exchanger in fluid-dense particle moving beds. Trans. of the ASME, J. of Heat Transfer. 89:1-60 - g5 - Sleicher, C. A., Jr. and M. Tribus. 1957. Heat transfer in a pipe with turbulent flow and arbitrary wall-temperature. Trans of the ASME. 79:789-797. 800, S. L. and J. A. Regalbuto. 1960. Concentration distribution in two-phase pipe flow. The Canadian Journal of Chem. Engr. 160- 166. 800. S. L. 1967. _F1uid Dynamics of Multi:phase Systems. Blaisdell Publishing Company. Toronto, London. Stoke, G. C., Cited by $00, 1967. Tchen, C. M. 1947. Cited by $00, 1967. Themelis, N. J. and W. H. Gauvin. 1963. Heat transfer to clouds of particles. The Canadian Journal of Chem. Engr. 1-6. Tien, C. L. 1960. Heat transfer by a turbulently flowing fluid-solids mixture in a pipe. Trans. of the ASME, Journal of Heat Transfer. 83C:183-188. Tien, C. L. and V. Quan. 1962. ASME Paper No. 62-HT-15. Cited by 800, 1967. Triebold, H. 0. and L. W. Aurand. 1963. Food Compnsition and Analysis. VanNostrand, Princeton, New Jersey. Wen, C. Y. and H. P. Simons. 1959. Flow characteristics in horizontal fluidized solids transport lines. Inc. & Eng. Chem. 53:51-53. Wilkinson. G. T. and J. R. NOrman. 1967. Heat transfer to a suspension of solids in a gas. Trans. Inst. Chem. Engrs. 45:T314-T318. Yannopoulos, J. C., N. J. Themelis, and W. H. Gauvin. 1966. An evaluation of the pneumatic transport reactor. The Canadian Journal of Chem. Engr. 231-235. Zabrodsky, S. S. 1966. Hydrodynamics and Heat Transfer in Fluidized Beds. The M.I.T. Press, Cambridge, Massachusetts, and London, England. (Translated by Zenz). Zenz, F. A. and D. F. Othmer. 1960. Fluidination and Fluid Particle Systems. Reinhold Publishing Corp., New York. Zenz, F. A. 1964. Conveyability of materials of mixed particle size. I and EC Fundamentals. 3(1):65-75. -86- APPENDICES - g7 - APPENDIX A SOLUTIONS FOR THE CASE OF UNIFORM WALL TEMPERATURE In equation (4-9) and (4-13), there exists three unknown such that equation (4-5) must be used to obtain the solutions of Ta and Tp. Before solving the governing equations, the following parameters should be defined: d (Re)d Pr m (Re) Pr m V p C w =._E_E_E p = AD V p C a a a 4h 4 4q = ____EL_. = _. w B1 v p c D D(St)m Be v p c D a a a a a h A B2 ' v p c = (St)dA a a a h A (St) A 3 V p C w P P P B = vapaca =___£__ 4 V p C + V p C 1 + w a a a p p p V p C B = P PHPI 5 V p C + V p C a a a P P P With the defined parameters, equation(4-5), (4-9), and (4-13) can be rewritten as: rm = 134 + BSTP ------------------------------------------ (A-l) dT a a: 7‘;- B1(Tw - Tm) - B2(Ta - TP) ------------------------- (A'Z) -88- dT __E = - ....................................... - dx B3(Ta Tp) (A 3) Equation (A-3) can be rearranged as: T =: a 3 By substitution of equation(A-l) into (A-Z), the new equation is dT __2 + ........................................ - dx Tp (A 4) w'H obtained as follows: dT a ———+ = - -------------- - dx (B2 + B1B4)Ta B Tw (B1B + BZ)Tp (A 5) l 5 Eliminating air temperature Ta from equation (A-5) with equation (A-4), the differential equation for particle temperature is: dZT dT + + + __2.+ = ------------- - dxz (32 B3 3134) dx BIBBTP 1311331:w (A 6) Equation (A-4) and (A-6) are the new governing equations. By using the method of operator, where m =-§§;2, equation (A-6) is written as: 2 = ................ .- [ m + (B2+B3+BIB4)m + 3133 JTP 311331:w (A 7) The solutions of equation (A-7) should be composited by the particular solution and complementary solution. The particular solution can be obtained by the method of undetermined coefficients. Let the particular solution and complementary solution by Y1 and Y2, respectively and let Y1 = C3, where C3 is constant. By substitution of Y1 into equation (A-7), the result is: = ----------------------------------------- A-8 C3BIB3 B1B3Tw ( ) - 39 - Therefore, the particular solution is: Y1 = C3 = Tw The complementary solution is obtained by the following procedures. Let m2 + (B2 +B +B1B4)m + B B = 0 --------------------------- (A-9) 3 1 3 The solution to the equation (A-9) is: -(B2+B3+B1B4) i: 2vrB2+B3+B14B - 43133 m = ------------ (A-10) The particle surface area per unit mixture volume is defined by equation (5-6). By substitution of equation (5-6) into parameter B 2 and B3, equation (A-10) can be simplified as: --(B2 +B 32'1'B1B4) ifBz +83 -B 134 )2 m = ---------------------- (A-ll) Therefore m = -(B +B )2 B B ------------------------------ (A-12) ’ 2 3 1 4 Since B1B2,B3, and B4 are real number, the complementary solution are two distinct real roots and can be written as: Y = ClExp [ -(B2+B3)x ] + c 2 Exp [ -B1B4x ] ------------- (A-13) 2 Then the complete solution for equation (A-6) is TP = Y1 + Y2 -------------------------------------------- (IX-14) or, Tp = ClExp [ -(B2+B3)x ] + c Exp [ -B1B4x ] + Tw ------- (A-15) 2 The boundary conditions of the system are: 0{T:= = Tp _____________________________________ (A-16) T31 l and C2 are determined to be: -(BlB4) (T -T w) - B 3(Tu-1:91) c1 = B ”+3 _B B -------------------- (A-17) 2 3 1 4 With the boundary conditions, C - 90 - _ (B2+B3)(Tpi-Tw) + (Tai-Tpi) - B +3 -3 B ----------------------- ' [(1+w) (Kai-T81) J ( 4(St)” x) a. .— Exp ._ ._._._._._.._ —— 1 Tpi-Tw (1+W) D 4w(St)m T .-T . ¢(1+w)(3t) _ pi a1 _ d x [9(l+w)(St)d (Tpi-Tw ) J Exp ( w D) } ......................... (A-Zl) - 91 - -T (St)d a w 9 ---- = (fl d) ( ) TPi-T ¢(l+w)(St)d 4(St)d w (1+w) , T i-Tai 4(St)m X i W [(1+W)-(fflf:E--)] EXP (- (1;;3"5 p1 w 4w(St)m 4w(St)m T .-T . [1-1 1 ~6—3i——§1) J 0(1-iw)(St)d 0(1+w)(St)d T .-T . p1 a1 0(1+W)(St)d x -. Exp 1 - w B J j ------------------------ (A'ZZ) In the case of the equal inlet temperature of both phases, equation (A-21) and (A-22) are simplified as follows: T -T (St) Tpi- w ( )( t)d - t m w (1+W) 4(St)!“ X 4W(St)m {11+W) EXP [-'fj:;3"53 ‘ p(1+w)(St)d J o<1+w)(5t)d EXP [ - w B] j ------ ' ------------------- (A-23) Eé_:_EE_ = ((S:)d *) ( p ) Tpi- Tw ”(1W)(St)d Egg-[B w - (1+W) 4(St)m x 4W(St)m {B(1+“) EXP [ (1+w) n 1 ' [1 ¢(1+w)(St>d J 4w(St)m ¢(1+W)(St)d x [Wig] Em- . 53} --------- (“4) - 92 - APPENDIX B SOLUTIONS FOR THE CASE OF LINEAR WALL TEMPERATURE With the parameters defined in Appendix A, equation (4-20), (4-5), and (4-13) can be written as: dT a _ _____________________ _ dx B1(Tai +'ax Tm) B2(Ta Tp) (B 1) = + .................................... .. Tm 34Ta BSTP (B 2) dT de =33“. - Tp) ------------------------------------ (B-3) 1 dT or, T = —- '—-B + T --------------------------------------- (B-4) a 3 dx p By substitution of equation (B-2) into (B-l), the new equation is obtained: dTa + (B2+B1B4)Ta + (BB 3;- anp = 31(Tai‘1'ax) -------- (Is-5) 1 5 Eliminating air temperature Ta from equation (B-5) with equation (B-4), the differential equation for particle temperature is: d2T —-£+(B23+B+BB)-E+BI3BT=BB(T.+X) ------- (B-6) dx2 1 4 3p 1 3 31 Equation (B-4) and (B-6) are the new governing equations. Using the method of operator gives: [m2231+(B+B+BB41)m+B1Bp3]T=BBBa(Ti+ax) ------ (B-7) - 93 - By comparison of equation (B-7) with equation (A-7), it is obvious that the complementary solution is exactly as same as that of case I which is: Y2 = ClExp [ -(BZ+B3)x J + C2Exp [ -B134x J ------------ (B-8) The particular solution can be obtained by the method of undetermined coefficients. Let the particular solution of equation (B-7) be: Y1 = C3 + Cax ------------------------------------------- (B-9) where C3 and C4 are arbitrary constant. By substitution of equation (B-9) into (B-7), it gives: ++ + [ (B2 B B B4)c4 BIB 3 1 ] + B B c x = B B T . + 3C3 1 3 4 1 3 a1 BlBjIX --------------------------------------------- (B-IO) Comparing the coefficients of equation (B-lO) gives: C =a ------------------------------------------------ (3'11) 4 (B 2+BB+B 18401 3 Tai ’ B1B3 """"""""""""""""" (3'12) C Equations(B-S),(B-ll), and (B-12) give the complete solution of the particle temperature, = - + + - Tp ClExp [ (B2 B3)x ] CZExp [ Blth ] + (B2+B3+B184)1 ax + T . - -------------------------- (3'13) a1 BlB3 The boundary conditions of the system are: Tp = Tpi x = 0, {T = T a ai With the boundary conditions, C1 and C2 are determined to be: - 94 - _ 1 Cl - (32+B3-B1B4) [ a +'(B3'B1B4)(Tp1 ' Tai) + (134 —§— (B2+B3+B1B4) J --------------------------------- (B-14) 3 l c=< )[-a+B(T.-T.)+ 2 32+B3 B1B4 2 p1 a1 (1 gig; (B2+BB)(BZ+BB+B1B4) J """""""""""""" (3'15) Therefore, the final solutions for air and particles are obtained: a 1 T -T . =(1x - —“- (3 +3 -B B ) + ( ) p 31 B1B3 2 3 l 4 B2+B3-B1B4 _Q__ { E ‘0' + B2(Tpi - Tai) + B B (B2+B3(B2+B3+BIB4) J 1 3 Exp [ -B1B4x ] + aB4 [ a I (B3’BlBa)(Tpi ' Tai) ‘ ‘3;— (Bz+B3+BlB4) J Exp 1 -(B,+B,>x J } -------------------------------- (B-Ie) a 81 1 3 2 3 1 4 {(53) [ +B (T -T ) +-—9H— (B +B )(B +B +B B ) ] B3 *1 2 pi ai B133 2 3 2 3 1 4 Exp [-BlB4x J + B -B B 3 1 4 _0_____. + - _ _ E ( 33 ) E a (B3 3134) (Tpi Tai) a34 '33- (32+BB+BIBA) J Exp [ -(BZ+B3)X } --------------- (B-17) -95- Now we substitute B parameters in terms of (St)m, (St)d, and w as defined in Appendix A, equation (B-l6) and (B-17) can be written in the dimensionless forms, T - T . (St) a a1 _ x ( w m w aD ” B'+ 4(St)m + 4 ' ¢(1+w)(sc)d) + [ 1 0(St)d 4(St)mJ 9d x } 4w(St)m ] Exp (-- w D ) ----------- (B-18) ¢(1+w)2(3t)d T - T . (St) __E_._ + .___JE - w ) + 4(St)m 4 0(1+w)(St)d E 1 —J M812)d 4(St)m ”(St)d + ’ (1+w)" , (rpi - Tai) ( 0(St)é - 4(St)-lE ) 1 dB w (1+W) 4w(St) 0(l+w)(St) m 1 Exp ( - w d g ) 1 ----------- (B-19) 11(1+w>2<3c>d X EXP ( - w 5 ) ---------------------------- (B-ZO) T -T . (St) a ££=§+__L_+__fl - W _ aD D 4(St)m 4 (0(1+w)(St:)d E 1 J [ <1-w) + 0(St)d 4(St)m ”(5% + “7;“ ' Tm)— 4w(St) 0(1+w)(St) m ] Exp ( - w d g ) ------------ (B-21) p<1+w)2<8t)d - 97 - APPENDIX C SOLUTIONS FOR THE CASE OF UNIFORM HEAT FLUX With the parameters defined in the Appendix A, equation (4-27) and (4-28) can be written as: dTa 75; = B6 - 32(Ta - Tp) --------------------------- (0’1) dT ——de = B3 (Ta - TP) ------------------------------------ (M) 1 dT = _ + ........................................ - or, Ta B3 '75? Tp (C 3) Eliminating air temperature Ta from equation (C-l) with equation (C-3) gives: d2T dT —d—}{'§ + (B2+B3) dx = B3B6 ---------------------------- (0-4) By using the method of operator, equation (C-4) can be written as: 2 1 m + (B2+B3)m J Tp = B236 ---------------------------- (c-s) The complementary solution of equation (C-5) is readily seen as: m = 0, -(B2+B3) Therefore, Y1 = c1 + C2Exp [ -(B2+B3)x ] --------------------- (C-6) The particular solution can be obtained with employing the undetermined coefficient method. Let the particular solution by Y2 = C3x. Sub- stituting Y into equation (C-4) gives: 2 B B C = 3 6 --------------------------------------------- (c-7) 3 B2+B3 The particular solution is then: The complete solution of equation (C-5) is obtained as: B3B6x = - + ................ .. Tp c1 + 02 Exp [ (B2 B3)x ] + 32+B3 (c 9) The boundary conditions of the system are: . Tp = TPi x = 0’ 1 T = . a 31 With the boundary conditions, C1 and 02 are obtained to be: _ BZTpi+B3Tai B3B6 c1 - B +3 - ——--§ --------------------------- (MD) + 2 3 (32 B3) B (T .-T .) B B CZ 23—9—2... +0197 ........................... (c-11) 2 3 (B2+B3) Therefore, the final solutions for air and particles are: B3 ’ Be . = (--- - (T .-T .) - ( p p1 32+B3 ‘1 p1 a1 B2+B3 ) + B6X + B 6 x [ (TP.-Tai) + B2+BB ] Exp [ -(B2_B3)x J j --------- (c-12) - 99 - B3 Be B6 Ta-Tpi - (B2+B3) 1 '(Tpi'Tai) ' (BE-TBS) + B; (1+8?) + B2 Be (3;) [ (Tpi-Tai) +‘E;;§; J Exp [ -(B2+B3)x ] } ----- (C-13) Substituting B parameters in terms of (St)m, (St)d, and w as defined in Appendix A, equation (C-12)and (C-13) can be written in the dimensionless forms, {Lies - _1._ {BB _ -__.4B_._ _ ‘Tpi'Tai’ + qw/GaCa 1 + w I) p(1+w)(sr.)d qw/GaCa [ (Tpi-Tai) 4W J qw/GaCa 0(1+w)(3t)d ¢(1+w)(5t)d EXP ( - “-T— B ) ,1 ------------------------- (C-14) 5-22.1 - __1-_ {52- w2 , $213.3_ qw GaCa 1 + w D 9(1+w)(St)d qw/GaCa w [ fzpi-TaiZ 4w 3 qw/caca ¢(1+w)(3t)d 0(1+W)(St) Exp ( - w d-E )} -------------------------- (C-15) If air and particle temperatures are equal at the entrance position, i.e. T . = Tai’ equation (C-14) p1 and (C-15) can be simplified as: T -T ..P_.L1.. ...1..- ”£5 _ ".4111.--“ qw/caca 1 + w 1 D 0(l+w)(St)d -100- (0(1+w)(3t)d 4w X (0(l-lw)(St)d) EXP (' w B ) 1 """""" (0'16) . 2 ._P.}. .-.l.. {333 - 4W .._ Q Ca 1 + w D 0(1+w)(St)d 4w mwxsod w (mm-ESE) Exp ( - w %)}--" (C-17) 101 0.0 000 0.00 0.00 0.0 0 0.000 0.00 0.000 0.0 000 0.00 0.00 00.0 00.0 0.000 0.00 0.00 0.000 0.0 000 0.00 0.00 00.0 00.0 0.000 0.00 0.00 0.000 0.0 000 0.00 0.00 00.0 00.0 0.000 0.00 0.00 0.000 0.0 000 0.00 0.00 00.0 00.0 0.000 0.00 0.00 0.000 0.0 000 0.00 0.00 0.0 0 0.000 0.00 0.000 0.0 000 0.00 0.00 0.0 0 0.000 0.00 0.000 0.0 000 0.00 0.00 00.0 00.0 0.000 0.00 0.00 0.000 0.0 000 0.00 0.00 00.0 00.0 0.000 0.00 0.00 0.000 0.0 000 0.00 0.00 00.0 00.0 0.000 0.00 0.00 0.000 0.0 000 0.00 0.00 00.0 00.0 0.000 0.00 0.00 0.000 0.0 000 0.00 0.00 00.0 00.0 0.000 0.00 0.00 0.000 0.0 000 0.00 0.00 00.0 00.0 0.000 0.00 0.00 0.000 00 x 0.0 000 0.00 0.00 0.0 0 0.000 0.00 0.000 00 00020 B0 0 .0.0.0 00000 000 00a 000 as 0.-~00-00\000 0000000 0. AouaumpmaEwH uw0cH 0m=vmV 00.15000 0