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EFFECT OF 000P-2509/791030I432SIS02 0010 FLUID DISPERSION COEFFICIENTS ON PARTICLE-TO-FLUID HEAT TRANSFER COEFFICIENTS IN PACKED BEDS CORRELATION OF NUSSELT NUMBERS N WAKAO,t S KAGUEI and T FUNAZKRI School of Engmeermg, Yokohama National Umverslty, Hodgaya-ku, Yokohama, Japan 240 (Recerued 24 February 1978. accepted 17 May 1978) Abstract-The pubhshed heat transfer data obtamed from steady and nonsteady measurements are corrected for the axial thud thermal dispersion coefficient values proposed by Wakao[ I] The corrected data m the range of Reynolds number from 15 to 8500 are correlated by the analogous form of the mass correlation proposed by Wakao and Funazkn[Z] Nu=2+ 1 1 Pr”)Reo6 This work for particle-to-flmd heat transfer 1s an ex- tenston of that reported by Wakao and Funazkn[2] m which the pubhshed particle-to-flmd mass transfer data were corrected for axial fluld dlsperslon coefficients Slmdarly to the data collectlon for mass transfer, we confine ourselves to the heat transfer measurements which satisfy the followmg condltlons 1 Particles m bed bemg all actlve 2 Number of particle layers m heat transfer bed being greater than two Table 1 summarizes the expenmentai condltlons of the collected measurements The data are shown as Nu vs Re m Fig 1 ConsIderable scattering and anomalous decrease m Nusselt number are seen at low Reynolds numbers In fact, the anomaly of Nusselt numbers has been a subject of dlscusslon for long However, not all the experimental mvestigators have supported the anomaly of Nusselt numbers From frequency response measurements, Llttman and Shva[3], and Gunn and De Souza[4] have estimated, respectively, from their own experiments the llmltmg Nusselt numbers of about 0 4 and 10 Some theoretical studies have also been made on this subject There IS, of course, no exact theory which describes the transport phenomena m packed beds Different theoretlcal estimates have given different hml- tmg Nusselt numbers Just hke the expenmental data, the two completely dIvergent conclusions have been drawn from the estimates Cormsh[S] indicates, assummg an analogy between electrostatics and heat, that the heat transfer coefficient m dense system of particles IS considerably smaller than that for a single sphere m an mfirute medium Kunu and Suzukl[6] pomt out that flow channeling m the bed IS the reason for the anomaly Nelson and Galloway [7] indicate that the anomaly IS explamed by a renewal of fluld tTo whom correspondence should be made element surrounding each particle Schlunder [8] shows, on the assumption that packed bed IS a bundle of parallel capillaries, that transfer coefficients decrease with a decrease of flow rate at lower Reynolds numbers On the other hand, Pfeffer and Happel[9] obtam, by applymg a free surface model, a lrmitmg Nusselt number of about 13 at the bed void fraction 0 4 From an analysis of steady transfer m a stagnant fluid m a concentrlc hollow sphere, Mlyauchl[lO] shows a hmltmg Nusselt number of about 18 at the bed void fraction 0 4 Stiren- sen and Stewart[ll] study a creepmg flow through a cubic array of spheres to find a hmltmg Nusselt number of about 3 9 Wakao et al [l, 12-141, however, find the defect of the fundamental equations responsible for the anomalous decrease m Nusselt number at lower Reynolds numbers REVIEW AND CORRECTI ON OF THE DATA OBTAINED FROM STEADY MEASUREMENTS Sdmultaneous heat and mass transfer study evaporatron of water and drfiusron-controlled chemrcal reactton on part&e surface The mass transfer data obtained from the stmultaneous heat and mass transfer studies have been used for the data correlation m the mass transfer paper[2] The cor- responding heat transfer data are, therefore, used m the present paper The data are those obtatned from the measurements of evaporation of water by Hougen et al [15, 161, Hurt[l7], Galloway et al [18], Thodos et al [19-231 and Bradshaw and Myers[24], and those determmed from the catalytic decomposltlon of hydrogen peroxide on metal spheres by Satterfield and Resmck[25] The measurements were made with sohd particles havmg codstant surface temperatures throughout the beds In the studies the system was described as dTF h,a U~+CbC.FU-~- T,.)=O 325 326 N WAKAO et al Kunu and Smith [271 C Cybulskl e/a/ C281 K Bradshow et al C461 L Hacdley and Hsggs C453 (Hougen eta/ Cl5. l-63 D Elchharn and White C301 E Llttman et o/ 1291 M F Gum and De Sauza 141 G Balokrlshnan and Pet C323 i Hurt Cl71 Galloway et a/ Cl81 Thadas et a/ 119-231 Brodshaw and Myers 1241 H Bhattacharyya and Pel m31 N Llndouer C471 I Glosw and Thodas 1351 0 Eaumslster and Bennett C3ll J Satterfleld and Resruck C251 P Turner et 01 C39. 401 A Liquid-Sdld B-P Gas-S&d FIN I Heat transfer data pubhshed In the literature and the heat transfer coefficients. h,, have been deter- mmed If, however, axial fluld thermal dlsperslon IS CO~SI- dered, the system IS ~TF h,a dZTF Udx+tEbCFPF(T~-Tps)=aox~ (2) The axial flmd thermal dlsperslon coefficient a,, has been consldered as a_ = (0 6- 0 8)aF m lammar flow range and aur = 0 SD,U m turbulent flow range, or ap- proximately over the range from lammar to turbulent (3) Wakao [ 11 and coworkers [ 12,141, however, recently pomted out that the heat transfer coefficients should be determmed from eqn (2) with the followmg ore values (as described later, this ts called the moddied D-C model) Instead of a._ of eqn (3) a&= k tax GCFQF (4) The axial fluid dlsperslon IS expressed by eqn (3), but the right hand side of eqn (2) should have sohd-phase conductlon contrlbutlon, as well as the dlsperslon m fluld phase Therefore, a Zz should rather be called the effective dlsperslon coefficient The heat transfer measurements revlewed m this sectlon have been made m the Reynolds number up to 8500 As far as the authors know, no measurements have been made on k,, at such high flow rates At htgh flow rates, however, the axial fluld dlsperslon IS, as described before, expressed as a Peclet number of two Equation (4) IS, therefore, rewritten as a%- k,” , GCFPF P (5) where k,” 1s the effective thermal conductlvlty of a stagnant packed bed Note that Wakao and Kato[26] have given a chart for esttmatmg k,” dues The heat transfer coefficients are recalculated from all of the steady heat transfer studies revlewed m thts section except the papers[l5, 17,241 m which no detalled data on bed height and/or void fraction are Gven The Effect of Ruld dlsperslon coefficients on particle-to-fluld heat transfer coeficlents m packed beds 327 Pr Walke and Hougen 1161 07 Sotterfteld and Resnick t251 IO Galloway el 01 Cl81 07 De Acetls and Thodos [I91 07 McConnoch~e and Thodos [211 07 Sen Gupta and Thodos C22, 231 07 Mollkng and Thodos I201 07 Nu-2+ I I Pr”3Rew, for Pr=07 Ag 2 Heat transfer data of steady state measurements corrected for azx correctlon procedure IS ldentmal wrth that employed m the mass transfer study[Z] except for the difference between heat and mass This IS briefly described m Appendix A The corrected data are plotted as Nu vs Re in Ftg 2 The solid lme shows the analogous form of the mass transfer correlation proposed m the work[2] Nu = 2 + I 1 Pr”3 Re”” (6) At lower Reynolds numbers the data are slightly higher than the solid line In fact, Sattertield and Resmck[25] have found Jr+/& = I 37, and De Acetls and Thodos[l9] JJJD = 1 5 1 McConnachle and Thodos [2l], Sen Gupta and Thodos[ZZ, 231, and Malhng and Thodos[ZO], however, have found JwlJD = I 0 In general, heat trans- fer measurements and determmatlon of heat transfer coefficients are more difficult than mass transfer studies Consldermg this, we may say that the heat transfer data shown m Fig 2 are well represented by eqn (6) Measurement of tetnperature m bed of no heat generating partrcles Kunu and Smlth[27], and Cybulskl et of [28], respec- tively,determined the heat transfer coefficients on the Continuous Solid Phase (C-S) model from the axml and radial heat transfer measurements Assuming that the gas temperatures computed on the C-S model are equal to the measured temperature profiles, Cybulskl et al obtam the coefficients Wakao et al [l3], however, pomt out that the C-S model can not be extended to the determmatlon of heat transfer coefficients at steady state In fact, under steady condlbon, the gas temperatures calculated with low heat transfer coefficrents on the C-S model agree with the temperatures computed on a smgle- phase model (m which heat transfer coefficient 1s not Involved, the temperature IS considered to be almost equal to the measured temperature), but the solid temperatures evaluated on the C-S model are far different from the temperatures on the single-phase model It IS considered that If Cybulskr et al had noticed the large difference m calculated temperature between the gas and solid, they have hesitated to determme the heat transfer coefficients Kunn and Smith also employ the C-S model In ad- dmon, they determine the anomalously low heat transfer coefficients by incorrect mterpretatlon of the algebraic relatIonshIp between the heat transfer coefficient and the effective thermal conductlvlty of the bed This has been cntlclzed by Llttman et al [29], and Gunn and De Souza[4] Gunn and De Souza point out that If Kunu et al had interpreted the algebraic relatlonshlp correctly, mfimtely large heat transfer coefficients would have been obtained As far as no heat source or smk exists m solid partl- cles, fluid- and sohd-phase temperatures under steady state condition are considered to be substantially the same Heat transfer coefficients cannot, therefore, be determined from the steady heat transfer measurements unless heat 1s generated or removed m solid particles Heat transfer between heat generatrng partrcles and fluid E~chhorn and Whlte[30], Baumelster and Bennett1311 and Pel et al [32,33] have employed high-frequency heating to generate heat m sohd particles Elchhorn and White find that the sohd temperature profiles are linear function of axial distance (see then Fig 3) The solid temperature at bed exit IS then estl- mated by the straight hne-extrapolation of the solrd temperatures to the exit They assume that the tempera- ture difference between the solid and gas throughout the bed IS the same as the difference between the solid temperature extrapolated to the bed exit and the 328 N WAKAO et QI Fig 3 Comparison Calculotm model Schumann with Nu - IO - Modlfled D-C Nu- I6 Modlfed D-C IW- 9 005 Modified D-C Mr= 12 002 Modlfed D-C Nu=23 002 Modbed D-C Nu=44 005 0 f. set of step response curves, lead-afr system, Re = 100, cb = 0 36, Dp = 0 3 cm, L = 3 3 cm, 3 1 cm2/sec a:= = temperature of the gas leaving the bed However, the temperature difference 1s small (0 9-3 8°F) and yet the solid temperature profiles seem to have relatively large errors (about 1°F m then Fig 3) compared to the temperature difference The obtained heat transfer coefficients are, therefore, considered to be less r&able Another reason for discarding their data 1s that the sohd temperatures may not be extrapolated to the bed exit Equations (Bl-3) solved with the Danckwerts’ boundary conditions show that both the sohd and gas temperatures should level off at the exit If this 1s the case, the temperature difference evaluated by Elchhom et al IS larger than the real temperature difference m the bed Note that the solid temperatures m the bed bemg hnear function of axial distance may ave an impression that the axial fluid dispersion coefficient IS small However, the substitution of cu& of eqn (5) mto eqn (B3), m fact, gives almost hnear increase of sohd temperature m the axial direction except m the vicuuty of the bed exit The data of Baumelster er al have been criticized by Jeff reson [34] because large temperature differences existed m radial direction of the bed Pel et al found the particle temperatures uniform throughout the beds and have calculated the heat transfer coefficients under the condition of uniform parMe temperature However, there may be a question whether a uniform temperature IS attamed by the unrform heat generatlon m particles In fact, as mentloned above, Elchhorn ef al found sohd temperature increase m the axial direction of the bed Baumelster et al have also observed considerable difference m sohd temperature between the bed inlet and outlet Glaser and Thodos[35] heated the particles by passing elecmc current directly through the bed of metaI spheres We are afraid, however, that heat must have generated at the points of partlcle contact and most of the heat transfer would have taken place near the contact pornts We, therefore, conclude that all of the data revlewed m this section should not be Included m the data cor- relation REVIEW AND CORRECTION OF THE DATA OBTAINED FROM NONSI’EADY MFASUREMENTS From step, frequency and shot response measure- ments, the heat transfer coefficients have been obtamed on any of the heat transfer models shown in Table 2 Schumann model, Contmuous Sohd Phase (C-S) model, and Dlsperslon Concentric (D-C) model The Schumann model [36] incorporates the following assumptions (I) Fluid IS m plug flow with no dlsperslon (II) No temperature gradient m particle The C-S model[29], when applied for axial heat trans- fer, has the assumptions (I) Fluid 1s m dispersed plug flow (11) Solid IS In axially contmuous phase through which heat conduction takes place m the axial direction The ortgmal D-C model and the modified D-C mode1[12, 141, both, have the assumptions (I) Fluid IS m dispersed plug flow (ii) Concentric temperature profile m particle The difference between the two models IS that the axial fluid drsperslon coefficient, a, of eqn (3), 1s used for the ongmal D-C model, while the large axial effective dispersion coefficient, aL of eqn (4), IS employed for the modified D-C model Gunn and De Souza[4] were the first to find, from the frequency response measurements, that the axial flmd thermal dispersion coefficients on the D-C model were considerably larger than those for extrapartlcle mass dispersion Vortmeyer(371 has discussed the meaning of the large dispersion coefficient values Wakao et al [38] have also obtamed, from the shot response measure- ments, the large thermal dlsperslon coefficients The C-S model has been cntlclzed by Kaguel et al [12], and the orlgmal D-C model by Wakao et al [ 1,141 They have shown that the moddied D-C model has advantage over the C-S and ongmal D-C models One of the important thmgs pomted out by them IS that the heat transfer coefficients determined on the C-S or original D-C model are different from those on the modified D-C model, particularly m the range of low Reynolds number The published nonsteady heat transfer data are, there- fore, converted mto those on the modified D-C model and compared with the steady heat transfer data recal- culated m the preceding section Note that the steady data have been reevaluated on the modtied D-C model Turner et al [39,40] and Gunn and De Souza[4] have obtamed, from the frequency response measurements, the heat transfer coefficients and the large axial dls- persion coefficients on the D-C model Their measure- Ta bl e I H ea t tr an sf er wo rk Ye ar Re fe re nc e Inv es tig at or Ex pe nA len ta I No me th od In de te mn at lon of he at Pa rt icl e tr an sf er co ef fic ien ts St ea dy or Flu td Pr Re fl ‘d Re ma rk s no ns te ad y Ma te ria l Sh ap e Siz e, nm Pa rt icl e dls p:: sio n te mo er at ur e co ns ide re d 19 43 ‘OS l G am so n , Ev ap or at ion of St ea dy Th od os an d w at er Ho ug en 19 43 [Iti Hu rt Ibi d St ea dy 19 45 D6 Ij W ilk e an d Ho ug en Ibi d St ea dy 19 52 @ I\ Oc hh or n an d Hig h fr eq ue nc y St ea dy W hit e die lec tr ic he at ing pa rt icl es 19 54 [a Sa tt er fle ld Ile co mp os lti on St ea dy an d Re sn lck of H2 02 19 57 [Id ] Ga lla ra y, Ev ap or at ion of St ea dy ko ma rn ick y w at er an d Ep st ein 19 58 &I Gla se r an d He at ing me ta llic St ea dy Th od os pa rt icl es by pa ss ing ele ct ric cu rr en t th ro ug h be ds 19 58 [3[ Ba um els te r Hig h fr eq ue nc y St ea dy an d Be nn et t tn du ct lon he at - lng pa rt icl es 19 60 [I$ De Ac et ls Ev ap or at ion of St ea dy an d Th od os w at er 19 61 [2f l Ku nil an d Ax ial he at St ea dy Sm ith co nd uc tio n in be ds 19 63 [21 /] Nc Co nn ac hle Ev ap or at ion of St ea dy an d Th od os w at er Ce l i t e Ce l fte Da re x- 50 ca ta lyt ic me ta l Sp he re 5 1 Va po r 1 0 mi xt ur e of H2 02 A H2 0 Ce l I te Sp he re 17 1 Ai r 0 72 Ma ne 1 Br as s St ee l Sp he re 4 8 Ai r 0 71 Sp he re 64 ,79 H2 0 72 co 2 0 67 Cy lin de r 6 4, 9 5 St ee l Cu be 6 4, 9 5 Sp he re 3 9, 6 3, 9 5 Ai r 07 Ce l i te Sp he re 15 9 Ai r 0 72 Gla ss Sa nd Sp he re 0 1, 0 4, 0 6, 1 0 He , Ai r, 0 1,0 2 C0 2, W at er Ce ll te Sp he re 15 9 Ai r 0 72 Sp he re 2 3, 3 0, 5 6. 8 4, Ai r 0 72 -O 75 D G 11 6 + 8 loo -4 ,00 0 Cy lrn de r 4 1x 4 8, 6 gX 8 5, ;*“ xl; 67 ; 14 ow l2 5, Cy lin de r 9 5x 9 5 Ai r 0 76 Cy lin de r 3 1x 3 1. 4 6x 4 3, Ai r 0 73 6 6x 7 2. 9 7x 8 6, 13 4x 12 8, 15 1x 16 3, 18 2x 16 9 Sp he re 0 1, 0 3, 0 4, 0 5, Ai r 07 07 co 2 08 y = 72 -9 50 T = 45 -2 50 La su re d y = 1-1 8 Su rf ac e at w et -b ulb te mp er at ur e as su ne d Me as ur ed y = 15 -16 0 Me as ur ed +G = 15 0- l ,20 0 4- G Me as ur ed Me as ur ed mw = IOO -9 ,20 0 Ap pa rt icl e su rf ac e ar ea w s ha pe fa ct or Su rf ac e at w et -b ulb te mp er at ur e as su ne d T = 20 0- 10 ,4 00 Me as ur ed y = 32 -2 ,10 0 Me as ur ed T = 0 00 1-l Co nt inu ou s so lrd ph as e w ith ax ial he at co nd uc tio n as su me d & = 110 -2 50 0 Me as ur ed No No No No No NO No No No Ye s NO He at tr an sf er co ef fr - cie nt s w er e no t de te r- mi ne d, bu t ob ta ina ble fr om th eir da ta Th e me as ur em en ts w er e cr ltr cr ze d by Lit tm an et a1 [29 ] Th e me as ur em en ts w er e cr l tlc rr ed by Je ffr es on [34 ] Th e an om alo us ly low Nu da ta w er e cr ltl clz ed by Ll tt ma n et a l[ 29 ] an d Gu nn et a1 [4 ] Ta bl e 1 ( Co nt d) In d et er mi na ti on of h ea t Pa rt ic le tr an sf er co ef fl cl en ts Ye ar Re fe re nc e In ve st ig at or Ex pe nm en ta l St ea dy or Fl wd Pr Re fl ' d Pa rW cl e dl sp :: s, on Re ma rk s NO me th od no ns te ad y M at er ia l Sh ap e Si ze , m m te mo er at ur e co wd er ed 19 63 I t2 41 B ra ds ha w an d Ev ap or at io n of St ea dy N ye rs 19 63 h ti Se n G up ta an d T ho do s 19 64 @ 3] Se n G up ta an d T ho do s 10 67 @ o] Ma ll ln g an d Th od os 19 67 [ 47 ] ti nd au er 19 68 [4 51 Ha nd le y an d He 99 s 19 68 [ 29 j 1i tt ma n, Ba ri le an d Pu ls if er 19 70 W I Br ad sh an . Jo hn so n, Mc La ch la n an d C hi u 19 71 [ 39 ] Go ss an d Fr eq ue nc y Tu rn er re sp on re wa te r Ib ld St ea dy Ka ol in e A M r Ka os or b Ce ll re Ce li te Ib id St ea dy Ce li te Ib ld St ea dy Ce ll te Fr eq ue nc y re sp on se No ns te ad y S te el Tu ng st en St ep re sp on se N on st ea dy St ee l Fr eq ue nc y re sp on se St ep re sp on se Le ad Br on ze So da gl as s Le ad gl as s Al um in a- si li ca No ns te ad y C op pe r Gl as s Le ad No ns te ad y A lu mi na St ee l He ma ti te No ns te ad y S od a 1 1m e gl as s Sp he re 4 7 Sp he re 8 8 Cy li nd er 4 0x 4 1 Cy li nd er 4 2x 4 2 . 6 2x 4 9 Sp he re 1 5 9 Sp he re 1 5 9 Sp he re 1 5 7- 15 g Sp he re 1 0 , 1 8, 3 2 Sp he re 0 5 Sp he re 3 2 , 6 4 , g 5 Cy li nd er 4 8x 4 8 , 6 4x 6 4 , 6 4x 12 7 Sp he re 3 0, 6l ,g l Sp he re 9 5 Sp he re 6 1 , 9 1 Sp he re 3 0 Sp he re 3 2 Sp he re 0 5 . 0 6, 0 7 , 1 I Sp he re 0 5 Sp he re 2 0 Sp he re 1 3 2 , 25 4 Sp he re 2 5 2 Sp he re 1 1 1 Sp he re 4 0 Bo ro sl ll ca te Sp he re 5 0 gl as s Me th yl Sp he re 4 8 ma th ac ry la te Ai r Ai r Ai r Ai r Ai r Ai r Ai r 07 0 72 0 72 0 71 07 07 07 Ai r Ai r, N2 0 74 07 ba su re d * 40 0- 6. 50 0 !!P ! u = &l o- 2, MK ) +$ = 2 ,O W6 ,0 00 y = lt 35 -8 ,5 00 y = 23 -l &2 00 OG + = GO -4 .0 00 La su re d H o La su re d H o Me as ur ed N o No t em pe ra tu re gr ad ie nt II I pa rt ic le as sf ae d No t em pe ra tu re gr ad ie nt in pa rt ic le +G = 2 -1 00 Co nt in uo us so li d ph as e w th a xi al he at co nd uc ti on as su me d & = 15 0- 60 0 t em pe ra tu re or of il e in _ Ce nt er -s yi mn et ri c ba rt lc le as su ne d DG Ce nt er -s yn me tn c -$ - = 1 ,6 00 -3 ,0 00 te mp er at ur e pr of Il e in pa rt ic le as sw d No N o No Ye s Ye s Ye s Th e d at a w er e c or re ct ed by Je ff re so nw ] f or fl ui d d is pe rs io n Th e R le th od of de te ni ni n N u d at a wa s 9 cr it ic ze d b y Ka gu el et a 1[ 11 2] 19 73 1 40 1 Tu rn er an d Fr eq ue nc y No ns te ad y S od a 1 1m e Sp he re 4 0 Ot te n re sp on se gl as s Ce ra mi c Sp he ro id 7 4 Si nt er ed 46 gl as s fe rt il iz er 31 Ir on or e 48 Ep ox y Sp he re 3 5 19 74 m ?] B al ak ri sh na n Mi cr ow av e St ea dy Ir on o xi de S ph er e 6 4 an d P ei he at in g pa rt ic le s Ni ck el ox id e S ph er e 6 4, 1 2 7 Va na di um SD he tX 4 8 pe nt ox Id e Cy li nd er 5 6x 5 6 , 5 6x 6 3 Ai r 07 Ce nt er -s ym me tr ic T = l, ZO O- 4, 60 0 t em pe ra tu re Ye s pr of ll e In pa rt ic le as su me d Ai r O' &= Me as ur ed Nl ck el - Cy li nd er 3 2x 6 4 mo ly bd en um ox id e Co ba lt - Cy li nd er 3 2x 6 4 am ly bd en mn Fr eq ue nc y No ns te ad y Gl as s Sp he re 0 3 , 0 5, 1 2 , 2 2, Ai r 07 re sp on se 30 .6 0 St ee l Sp he re 3 2, 63 Le ad Sp he re 0 8 19 75 1 4 Bh at ta ch ar yy a Mi cr ow av e St ea dy fe rr ic ox id e S ph er e 3 2, 7 6 Ai r 07 an d P ei he at in g pa rt ic le s Cy li nd er 5 1x 5 1 19 15 l 2q Cy bu ls ki , Ra di al he at St ea dy Si li co n- fF "" - O ’ Ai r 07 Va n O al en , co nd uc ti on capp er Ve rk er k an d In be ds Va n D en Be rg 19 76 [ w Wa ka o, Sh ot re sp on se N on st ea dy Po ly st yr en e Sp he re 0 8 Ai r 07 Ta ni sh o an d Sh io za wa Gl as s Sp he re 0 3, 11 .1 6 Le ad Sp he re 0 9 34 0- 4. 40 0 OG + = 0 05 -3 30 $G = 1 10 -8 30 OG $ = 0 24 -O 64 DG + = 0 2- 6 Ce nt er -s ym me tr ic te mp er at ur e or of il e in pa rt ic le as su me d Ue as ur ed Co nt in uo us so li d ph as e w it h r ad ia l he at co nd uc ti on as su ne d Ce nt er -s yn mt et ri c te mp er at ur e pr of il e In pa rt ic le as su me d No Ye s NO No Ye s Nu ss el t nu mb er s at Re -a/ r at- ._ at r = R. aTS ks(--$ = hp(TF-Ts) ments obviously support the modified D-C model, but theu data are examined m sensitlvlty Step response Step response measurements were made by Furnas[41], Saunders and Ford [42]. Lof and Hawley[43]. Coppage and London[44], Handley and Heggs[45], and Bradshaw et al [441 Except Bradshaw et al who employed the D-C model. all of them have determmed the heat transfer coefficients on the Schu- mann model However, m the early stuches[414l] the heat transfer coefficients seem to have been determined by less reliable graphIcal method The data of the two relatively recent measurements, Handley ef al [453 and Bradshaw et al [&I, are reevalu- ated on the modified D-C model Handley et al have obtamed the heat transfer coef?icIents on the Schumann mode1 The exact solution to a step response IS shown m Appendix D Usmg the Schumann model solution, the response curves T,(t) of Handley et al are predicted with the data reported in their paper The response curves TZ( t) are also calculated on the mod&d D-C model wrth vaned heat transfer coefficient values Figure 3 illustrates the comparison of T,(f) and IQ(t) The error es IS calculated by where we choose the times. 7, and 7*, respectively. as T&T,) = 0 05 To and T=(T~) = 0 95 To We may probably say that the agreement of the two curves IS good when l sFig 9, the valley with the error 0 05 IS steep As far as the example is concerned, the determined Nusselt number IS consi- dered to be enough reliable I In fact, the experiments of Turner et al were conduc- ted at high Reynolds numbers 1200-4600 As mentioned already, reliable heat transfer coefficients are determined at high flow rates The data of Turner et al are, there- fore,-included in our data correlation Id I II, Fig 9 Error map for a simulation illustration of Goss and Turner[391 (+ shows the data obtamed by them), Re = 950, o = 0 5 rad/sec, other data shown in theu Table 1, a:, of eqn (5) = 250 cm2/sec Shot response From the analysis of shot response measurements, Wakao et al [l, 381 examined the heat transfer coefficients on the modified D-C model, pointing out the advantage of the model No definite Nusselt numbers were obtained, but they have found that Nusselt numbers were considered to be in the range from 0 1 to m at Reynolds numbers 0 24 ex$ession of mass correlation, eqn (6) - I I 7 CORRELATION OF NUSSELT NUMBERS From the review in the preceding sections the heat transfer data which have passed our criteria are [16, M-23, 25, 39. 40, 45, 463 Their heat transfer coefficients reevaluated on the modified D-C model are plotted in Fig 10 The data are well reoresented bv the analogous L e 0 - + D 14 - I> V A NU 10 - Steady state Wllke and Hougen Cl61 Satterf@d and Resnrk C251 Galloway eZ a/ Cl81 De Acetls and Thodos Cl91 McCo-he and Thodos C211 Sen Gupta and Thodos C22. 231 Mallmg and Thadas C201 Nonsteady state l Hand!ey and Heggs L451 N&,=2+1 lPr”sR&s I Bradshow ef o/ C461 . Goss and Turner C391 A Turner and Otten [401 IO 10- ID- IO- Id (Pr”%M v Fig 10 Correlation of reevaluated Nusselt numbers Effect of tluld drsperslon coetliclents on particle-to-flutd beat transfer coefficrents m packed beds 335 One more thmg we have to pay attention to IS that Ftg 1 shows the mixture of heat transfer data obtamed on the different models Some of them are, as mentioned al- ready, less rehable and some have been crltlclzed on the calculation procedure COIWLUSIONS 1 The published heat transfer data are corrected for the ax&al fluid thermal dlsperslon coefficients proposed by Wakao[l 1 The reevaluated data on the mod&d D-C model are correlated by the analogous form of the mass transfer correlation, eqn (6) 2 When the heat transfer correlation 1s used for the design and analysis of packed bed reactors, the axial effective thermal dlsperslon coefficients gven by eqn (4) should also be employed a CF CS DP G h, h;, JrhJw ke" k aax k ef k es k, ks L Nu Pr R Rd TF Tk TL Tt NCYTATION partlcle surface area per umt volume of packed bed specific heat of fluid specific heat of sohd particle diameter ~,bupF, fluld mass velocrty heat transfer coefficient heat transfer coefficient determmed with aaX = 0 J-factors, respectively, for mass and heat effective thermal conductlvlty of packed bed with stagnant fluld axial effective therma conductlvlty of packed bed effectlve fhud thermal conductlvlty effective sohd thermal conductlvlty fiuld thermal conductlvlty sohd thermal conductlvlty packed bed helgkt hPDJkF, Nusselt number C&kF, Prandtl number partrcle radms radial distance variable D+bUpJp, Reynolds number fhud temperature Inlet fluId temperature fluid temperature at bed exit fluld temperature at bed exrt calculated on modified D-C model fluld temperature at bed exit calculated on D-C model with varied crrx and Nu temperature change Imposed on tnlet fluid temperature on particle surface sohd temperature amplitude m complex ttme mterstttlal fluid velocity axial distance variable Greek symbols aar axial fluld thermal dlsperslon coefficrent a?; axml effective thermal dlsperslon coefficient, defined by eqn (4) aF fluld thermal drffuslvlty as sohd thermal dlffuslvlty Q bed void fraction 4 error defined by eqn (8) eS error defined by eqn (7) pF flurd denstty PS sohd density 7,, 72 trmes p fluld vlscoslty w frequency REFERENCES [l] Wakao N, Chem EngngScr 197631 1115 [2] Wakao N and Funazti T, Chem Engng Scr 1978 33 1375 131 Lntman H and Shva D E . Proc Int’l Heat Transfer Conf Versailles, Paper CT1 4 (1970) r41 Gunn D J and De Souza J F C Chem Engng Scd 1974 29 - 1363 [5] Cormsh A R H , Trans Instn Chem Engrs 1%5 43 T332 161 Kunu D and Suzuki M . Inl J iYear Mass Truns 1%7 10 _ - 845 [7] Nelson P A and Galloway T R , Chem Engng Scr 1975 30 1 [8] Schlfinder E U , Chem Engng Scl 1977 32 845 191 Pfeffer R and Happel J , A ICh E J 1964 10 605 [lo] Mlyauchl T , J Chem Engng Japan 1971 4 238 [I I] Serensen J P and Stewart W E , Chem Engng Scr 1974 29 827 [12] Kaguel S , Shrozawa B and Wakao N , Chem Engng SCI 1977 32 507 [ 131 Wakao N , Kaguel S and Nagal H , Chem Engng Scr 1977 32 1261 [14] Wakao N , Kaguel S and Shlozawa B , Chem Engng Scl 1977 32 451 [IS] Gamson B W , Thodos G and Hougen 0 A, Truns Am Inst Chem Engrs 1943 39 1 [16] Wllke C R and Hougen 0 A. Trans Am Insl Chem Engrs 1945 41 445 [17] Hurt D M , Ind Engng Chem 1943 35 522 [18] Galloway L R , Komarmcky W and Epstem N , Con J Chem l&n= 1957 35 139 [I91 1201 PII WI WI ~241 [251 [261 [271 [=I r291 r301 [311 ~321 r331 [341 f351 K361 [371 r3g1 [391 (401 De Acetlsj and Thodos G , Ind Engng Chem 1960 52 1003 Malhng G F and Thodos G , Inf J Heat Mass Truns 1%7 IO 489 McConnachle J T L and Thodos G , A Z Ch E J 1963 9 60 Sen Gunta A and Thodos G , A I Ch E3 1963 9 751 Sen Gupta A and Thodos G , Ind Engng Chem Fundls 1964 3 218 Bradshaw R D and Myers J E t A ICh EJ 1963 9 590 SattertIeld C N and Resmck H , Chem Engng Progr 1954 50 504 Wakao N and Kato K , J Chem Engng Japan 1969 2 24 Kunu D and Smith J M , A I Ch E J 1961 7 29 Cybulskl A, Van Dale” M J . Verkerk J W and Van Den Berg P J Chem Engng Scr 1975 30 I015 Lrttman H , Barde R G and Pulsifer A H , Ind Engng Chem Fundls 1%8 7 554 Erchhorn J and White R R , Chem Engng Progr Symp Ser 195248(4) 11 Baumelster E B and Bennett C 0 , A ICh E J 1958 4 69 Balakrlshnan A R and Pel D C T, Ind Engng Chem Proc Des Da, 197413441 Bhattacharyya D and Pel D C T , Chem Engng Scr 1975 30 293 Jeffreson C P A ICh El 1972 18 409 Glaser M B and Thodos G , A I Ch E J 1958 4 63 Schumann T E W , / Frankfm hsl 1929 2@ii 405 Vortmeyer D , Chem Engng Scl 1975 30 999 Wakao N , Tamsho S and Shlozawa B , Kogaku Kogaku Ronbunshu (Japan) 1976 2 422 GossM J andTumerG A AfChEJ 1971 175% Turner G A and Otten L , Ind Engng Chem Proc Des Dev 1973 12 417 336 N WAKAO et al I411 Furnas C C , Ind Engng Chem 1930 22 721 [421 Saunders 0 A and Ford H , J Iron SteelInsr 1940 141 291 [43] Lof G 0 G and Hawley R W , Ind Engng Chem 1948 40 1061 [441 Coppage J E and London A L Chem Engng Progr 1956 52 57-F [451 Handley D and Heggs P J Trans Instn Chem Engn 1968 46 TZSI r461 Bradshaw A V , Johnson A McLachlan N H and Chm Y-T Trans Instn Chem Engrs 1970 48 T77 I471 Lmdauer G C , A ICh El I%7 13 I181 APPENDIX A STEADY HEAT TRANSFER B ETWRRN FLUID AND PARTlCLE SURFACE AT CONSTANT TEMPERATURE For heat transfer between thud and particles havmg constant surface temperature T,, throughout the bed of finite length, the change m thud temperature IS given by (refer to eqn (7) m 121) Tm - TL = 4Aev 2rrw L-1 T,, - Ttn (t +A)‘exp[A&]-(l:)‘exp[-A$$] where When n:, = 0 eqn (Al) reduces to T’s - TL _ Tps - T,, - exp h;aL - CCZJCFQF 1 ConversIon of h; into h, IS, therefore made (Al) and (A2) (Al) (A3 by equating eqns APPENDIX B STEADY HEAT TRANSFER FROM HEAT GENERATING PARTKLES When heat 1s generated at constant rate m particles the flmd and sohd temperatures m the bed of finite length are TF = T,,++(&)(+) and x[f+$(l-‘=P[-~(l-;)])] (RI) T,= T+@+*(R’-9) 3h, 6ks where q = heat generatlon rate per umt volume of particleThe sohd temperatures Elchhorn and WhrteI301 claim_ to have measured are the particle-volume-mean-temperatures Ts (B3) APPENDIX C FREQUENCY RESPONSE For the fundamental equations hsted m Table 2, the boundary condltlon on the Schumann model IS atx=O TF = Re [fOeelp)#] (Cl) and those on D-C model are at x = 0. U(TF - Re f?Oel”‘]) = a., % aTF=O (C2) atx=L dX When the stationary solution of TF at x = L 1s expressed as TL = Re [ fL cur] (C3) on Schumann model f,+ IS %=exp[-+(I+-$-)] (C4) where k,= h*a (I- 4CsPs and on D-C model, UL . TL= exp - [ 1 TO cash 2,~1+8)]+~slnh,~,lts)l C 0.X where 1 I t$ coth r$ - 1 In both Schumann and D-C model, the error Ed of eqn (8) IS W4 Using eqn (Cl), Gunn et al [41 have obtained the semi-mtimte solution of the fundamental equations f f=exp TO C, e (I- ~‘(1 + B))] (C7) APPENDIX D Sl%P RESPONSE The mltial and boundary condlttons for Schumann model are at f=O, TF = 0 at x =0, TF = T,, I WI) and those for D-C model are at f=O, TF = 0 at x = 0. U(T,z - To) = a_ % (D2) at x = L, aT,=O l%X The solution IS TL=l+22 ’ ---Im [ (2) eUf],=, TO 2 ?r,,=,2n-I (D3) where w. = (2n - I)F/$and lo IS a time sufficiently long enough to attam Tr = To TJTo IS given for Schumann model by eqn ((24) and for D-C model by eqn (C5) The error of eqn (7) IS approximately expressed as