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Nomenclature

Nomenclature

Chapters 1 through 18

ainterfacial area per volume, ft2/ft3 or m2/m3
interfacial area for heat transfer on stage j, m2
aflow, aheat, amasseddy diffusion parameters, Eqs. (15-48)
apsurface area/volume, m2/m3
ap1, ap2, ap3, aT1, aT2, aT6constants in Eq. (2-30) and Table 2-3
Aarea, m2
A,B,Cconstants in Antoine Eq. (2-34)
A,B,C,D,Econstants in Eq. (2-60)
A,B,C,Dconstants in matrix form of mass balances, Eqs. (6-13) and (12-58)
AE, BE, CE, DEconstants in matrix form of energy balances, Eq. (6-34)
Aactiveactive area of tray, ft2 or m2
Accross-sectional area of column, ft2 or m2
Addowncomer area, ft2 or m2
Aduflow area under downcomer apron, Eq. (10-28), ft2
Afarea for flow, m2
Aholearea of holes in column, ft2
AIinterfacial area between two phases, ft2 or m2
Amixercross-sectional area of mixer, m2
Anetnet area, Eq. (10-13), ft2 or m2
bempirical constant, Eq. (13-63b)
bequilibrium constant for linear equilibrium, y = mx + b
bflow, bheat, bmasseddy diffusion parameters, Eqs. (15-48)
Bbottoms flow rate, kmol/h or lbmol/h
Cnumber of components
CBMbare module cost, Chapter 11
CCconcentration of solute in continuous phase, kmol/m3 continuous phase
concentration of solute in continuous phase in equilibrium with CD, kmol/m3
CDconcentration of solute in dispersed phase, kmol/m3 dispersed phase
CfLvapor load coefficient, Eq. (15-38)
CA, CB, Cmmolar concentrations, of A, B, and mixture, mol/m3
Coorifice coefficient, Eq. (10-25)
Cpheat capacity, Btu/lb°F or Btu/lbmol°F or cal/g°C or cal/mol°C, etc.
Cpbase purchase cost, Chapter 11
Cp,sizepacking size factor, Table 10-5
CpWwater heat capacity
Cscapacity factor at flood, Eq. (10-48)
Csbcapacity factor, Eq. (10-8)
ddampening factor, Eq. (2-57)
Ddiffusivity, Fickan m2/s or ft2/h
Ddistillate flow rate, kmol/h or kg/h
D, Diadiameter of column, ft or m
D’colcolumn diameter, see Table 16-1, ft
dhydraulichydraulic diameter of drop, Eq. (13-62), m
diimpeller diameter, m
dp, dddrop diameter, m
characteristic drop diameter, Eq. (16-97b), m
dtubetube diameter, m
dsettler, Dsdiameter of horizontal settler, m
Dlarge, Dpilotdiameters of Karr columns for scale-up, Eq. (13-66), m
infinite dilution Fickian diffusivity, m2/s
DMaxwell-Stefan diffusivity, m2/s
Deddyeddy diffusivity, Eq. (16-111a, b), m/s
Dtotaltotal amount of distillate (Chapter 9), moles or kg
eabsolute entrainment, mol/h
eplate fractional free area in Karr column
erferror function, Eq. (18-70)
Eextract flow rate (Chapters 13 and 14), kg/h
Êmass extract, kg
energy transfer rate on stage j from bulk liquid to bulk vapor, J/s
Ekvalue of energy function for trial k, Eq. (2-51)
EML, EMVMurphree liquid and vapor efficiencies, Eqs. (4-58) and (4-59)
E0activation energy, Kcal/mol
EoOverall efficiency, Eq. (4-56)
Eptpoint efficiency, Eq. (10-5) or (15-76a)
Êtholdup extract phase in tank plus settler, kg
ffriction factor
fABfriction coefficient between molecules A and B
f = V/Ffraction vaporized
ffractional approach to flooding
ffrequency of reciprocation of Karr column, strokes/s
f(x)equilibrium function, Chapter 9
fk(V/F)Rachford-Rice function for trial K, Eq. (2-43)
Fpacking factor, Tables 10-3 and 10-4
Fdegrees of freedom, Eq. (2-4)
Fcharge to still pot (Chapter 9), moles or kg
Fmass of feed in batch extraction, kg
Ffeed flow rate, kmol/h or lbmol/h or kg/h etc.
FDdiluent flow rate (Chapter 13), kg/h
Flv, FP, flow parameter
Fmmaterial factor for cost, Table 11-2
Fppressure factor for cost, Eqs. (11-5) and (11-6)
Fqquantity factor for cost, Eq. (11-7)
Fs,Fsolvflow rate solvent (Chapter 13), kg/h
Fsolidsolids flow rate in leaching, kg insoluble solid/h
Fweirweir modification factor, Eq. (10-26) and Figure 10-22
gapgap from downcomer apron to tray, Eq. (10-28), ft
gacceleration due to gravity, 32.2 ft/s2, 9.81 m/s2
gcconversion factor in English units, 32.2 ft·lbm/(lbf·s2)
Gflow rate carrier gas, kmol/h or kg/h
G′gas flux, lb/s ft2
hpressure drop in head of clear liquid, inches liquid
hheight of liquid on stage (Chapter 16), ft
hheight, m or ft
hheight of liquid in mixer, m
hliquid enthalpy, kcal/kg, Btu/lbmol, etc.
hstep size in Euler’s method = Δt, Eq. (8-29)
pure component enthalpy
hfenthalpy of liquid leaving feed stage
hFfeed enthalpy (liquid, vapor or two-phase)
hheat transferheat transfer coefficient
hLclear liquid height on stage, m or cm
hohole diameter, inches
hppacking height, ft or m
htotalheight of flash drum, ft or m
hwheight of weir, m or cm
HHenry’s law constant, Eqs. (8-9), (8-10), and (12-1)
Hmolar holdup of liquid on tray, Eqs. (8-27) and (8-28)
Hstage height in Karr column, m
Hvapor enthalpy, kcal/kg, Btu/lbmol, etc.
partial molar enthalpy of component i in vapor on stage j, J/kmol
height of tank, m
Ht,ODoverall height of a transfer unit for mass transfer driving force in concentration units, Eq. (16-83a analog), m
HGheight of gas phase transfer unit, ft or m
HLheight of liquid phase transfer unit, ft or m
HOGheight of overall gas phase transfer unit, ft or m
HOLheight of overall liquid phase transfer unit, ft or m
HETPheight equivalent to a theoretical plate, ft or m
HTUheight of a transfer unit, ft or m
jD, jHj-functions, Eqs. (15-50)
JAflux with respect to molar average velocity of fluid
k1, k2empirical constants, Eq. (13-63b)
kBBotzmann’s constant, J/k
kconductionthermal conductivity, J/(ms K)
individual mass transfer coefficients in liquid and vapor phases, see Table 15-4
kcmass transfer coefficient with concentration driving force, m/s, Eq. (15-25b)
k’ymass transfer coefficient in concentrated solutions, Eq. (15-32f)
kx, kyindividual mass transfer coefficient in molar units
kx,c, kxDindividual mass transfer coefficients in continuous and dispersed phases, kg/(s·m3) or kmol/(s·m3)
kLD, kLCindividual mass transfer coefficients in continuous and dispersed phases with driving force in concentration units, m/s
kL, kVindividual liquid and vapor mass transfer coefficients in distillation, Eq. (16-108), m/s
kmass transfer coefficient in Maxwell-Stefan analysis, Đ/Δz, m/s
Kdy/x, distribution coefficient for dilute extraction
K, Kiyi/xi, equilibrium vapor-liquid ratio
Kdrumparameter to calculate uperm for flash drums, Eq. (2-64)
Kx, Kyoverall mass transfer coefficient in liquid or vapor, lbmol/ft2 h, or kmol/h·m2
KLDoverall mass transfer coefficient in extraction based on dispersed phase in concentration units, Eq. (16-80b analog), m/s
KO-EDoverall mass transfer coefficient in extraction based on dispersed phase, Eq. (16-80a), kg/(s·m3) or kmol/(s·m3)
lwweir length, ft
Llength, m
Lliquid flow rate, kmol/h or lbmol/h
mass liquid flow rate, lb/h (Chapter 15)
L′liquid flux, lb/(s)(ft2)
Lgliquid flow rate in gal/min, Chapter 10
mlinear equilibrium constant, y = mx + b
mlocal slope of equilibrium curve, Eq. (15-30b)
Mratio HETPpractical/HETPpacking Eq. (10-46)
mCDslope of equilibrium curve of continuous versus dispersed phase mass or mole fractions, Eq. (16-80c)
mCD,conc_unitsslope of equilibrium curve of continuous versus dispersed phase in concentration units, Eq. (16-80c analog)
Mflow rate of mixed stream (Chapter 13), kg/h
Mmultiplier times (L/D)min (Chapter 7)
MWmolecular weight
average molecular weight
nmoles
nnumber of drops
n1, n2empirical constants, Eq. (13-65)
nGnumber of gas phase transfer units
nLnumber of liquid phase transfer units
nO-ED, nO-ECnumber of overall extraction transfer units in dispersed and continuous phases, Eq. (16-81)
nOGnumber of overall gas phase transfer units
nOLnumber of overall liquid phase transfer units
norgmoles organic in vapor in steam distillation
nwmoles water in vapor in steam distillation
Nimpeller revolutions per second
Nnumber of stages
NAflux of A, lbmol/(h)(ft2) or kmol/(h)(m2)
Nf,Nfeedfeed stage
transfer to liquid from vapor on stage j, mol component i/s
transfer to vapor from liquid on stage j, mol component i/s
Nminnumber of stages at total reflux
Nfeed,minestimated feed stage location at total reflux
NPopower number, Eq. (13-52)
NtODnumber of overall extraction transfer units for mass transfer driving force in concentration units, Eq. (16-81a analog)
NuNusselt number, Eq. (15-33g)
NTUnumber of transfer units
Ototal overflow rate in washing, kg/h
ppitch of sieve plate holes, m
p, ptotpressure, atm, kPa, psi, bar etc.
, pBpartial pressure
PNumber of phases
Ppower, W
Pedimensionless Peclet number in terms of molecular diffusivity, Eq. (15-33c)
Pedimensionless Peclet number in terms of eddy diffusivity, Eq. (16-111a)
Perfflow perimeter, Figure 13-33B, m
Prdimensionless Prandt number, Eq. (15-33f)
qLF/F = (L – L)/F, feed quality
qvolumetric flow rate/plate width, m2/s
Qamount of energy transferred, Btu/h, kcal/h, etc.
Qccondenser heat load
Qc, QCvolumetric flow rate continuous phase, m3/s
Qd, QDvolumetric flow rate dispersed phase, m3/s
Qflashheat loss from flash drum
QLvolumetric flow rate of liquid, m3/s
QRreboiler heat load
Qzheat flux in z direction, J/s
rradius of column, ft or m
Rgas constant, 1.9859 cal/(mol·K) or 8.314 m3Pa/(mol·K)
Rraffinate flow rate (Chapter. 13), kg/h
RAsolute radius, m
mass raffinate, kg
Holdup raffinate phase in tank plus settler, kg
Redimensionless Reynolds number, Eq. (15-33b)
ResettlerReynold’s number for settler, Eq. (13-60a)
Ssolvent flow rate kmol/h or lbmol/h
Stray spacing, inches, Eq. (10-47)
Smoles second solvent in constant-level batch distillation
Ŝmass of solvent, kg
Ssolvent flow rate, kg/h
ScLSchmidt number for liquid = μ/(ρD)
ScvSchmidt number for vapor = μ/(ρD)
Shc, Shx, Shydimensionless Sherwood numbers, Eq. (15-33a)
Stc, Stx, Stydimensionless Stanton numbers, Eq. (15-33d)
ttime, s, min, or h
tbatchperiod for batch distillation, Eq. (9-28)
tdowndown time in batch distillation
(tf,95 – t0)residence time in extractor for 95% extraction, Eq. (16-105), s
tL, tVaverage residence time per pass for liquid and vapor, s
,residenceliquid residence time, Eq. (16-111c), s
tresidence,dispersedresidence time of dispersed phase in settler, s
toperatingoperating time in batch distillation
tresresidence time in downcomer, Eq. (10-30), s, or on plate, Eq. (16-35e)
ttraytray thickness, inches
Ttemperature, °C, °F, K, or °R
liquid and vapor temperatures on stage j at the interface, K
Trefreference temperature
uvapor velocity, cm/s or ft/s
ufloodflooding velocity, Eq. (10-8)
uopoperating velocity, Eq. (10-11)
upermpermissible vapor velocity, Eq. (2-64)
ut,hinderedhindered settling velocity, Eq. (13-58)
ut, ut,StokesStokes’ law terminal velocity, Eq. (13-57), m/s
Uunderflow liquid rate, (Chapter 14), kg/h
Uasuperficial vapor velocity in active area of tray, m/s
vsuperficial vapor velocity, ft/s
vcharacteristiccharacteristic velocity of Karr column, Eq. (13-68), m/s
vc,flood, vd,floodcontinuous and dispersed phase flooding velocities, m/s
vovapor velocity through holes, Eq. (10-29), ft/s
vo,balvelocity where valve is balanced, Eq. (10-36)
VA, VBcomponent transfer velocities, Eqs, (15-15e, f)
vrefreference or basis velocity, Eqs. (15-15c, d)
vyvertical velocity
Vvapor flow rate, kmol/h or lbmol/h
Vimolal volume Eq. (13-1)
VAmolar volume solute at normal boiling point, m3/kmol
Vliq,tankvolume of liquid in tank, m3
Vmaxmaximum vapor flow rate
Vmixervolume of liquid in mixing tank, m3
Vsettlervolume settler, m3
Vtankvolume tank, m3
Vsurgesurge volume in flash drum, Eq. (2-68), ft3
VPvapor pressure, same units as p
wplate width, m
WLliquid flow rate, kg/h or lb/h
WLliquid mass flux, lb/s ft2 or lb/h ft2, (Chapter 16)
WVvapor flow rate, kg/h or lb/h
xweight or mole fraction in liquid
x[L/D – (L/D)min]/(L/D + 1) in Eqs. (7-42)
x*equilibrium mole fraction in liquid
xA,ref, xB,reffractions to calculate velocity of center of total flux, Eq. (15-17)
xi,k, xi,k+1trials for integration, Eq. (8-29)
xIinterfacial mole fraction in liquid
x*outliquid mole fraction in equilibrium with inlet gas, Eq. (16-35b)
Xweight or mole ratio in liquid
yweight or mole fraction in vapor
yvolvolume fraction in vapor
y*equilibrium mole fraction in vapor
y*outvapor mole fraction in equilibrium with inlet liquid in countercurrent system, Eq. (16-35a) or in equilibrium with outlet liquid in cocurrent contactor, Eq. (16-71)
ylmlog mean difference, Eq. (15-32d)
yIinterfacial mole fraction in vapor
mass fraction in vapor
Yweight or mole ratio in vapor
zweight or mole fraction in feed
zaxial distance in bed (Chapters 15 and 16)
zldistance from downcomer exit to weir, m


Greek

αABKA/KB, relative volatility
αthermalthermal diffusity, m2/s
βAhole/Aactive
γactivity coefficient
δthickness of mass transfer film or thickness of falling film, m
δpcharacteristic dimension of packing, inch, Eq. (10-38)
δisolubility parameter, Eq. (13-1)
Δchange in variable or difference operator
ΔEvlatent energy of vaporization, Eq. (13-1)
ΔHsteady state height of dispersion band in settler, m
ΔρC - ρD|
εlimit for convergence
εAB, εABLennard-Jones interaction energies, Table 15-2 and Eq. (15-22c)
ηfraction of column available for vapor flow
ηparameter, Eq. (15-42b)
θangle of downcomer, Figure 10-20B
λlatent heat of vaporization, kcal/kg, Btu/lb, Btu/lbmol, etc.
μviscosity, cp or Pa·s = kg/(m s)
μwviscosity of water, cp
ρLliquid density, g/cm3 or lb/ft3 or kg/m3
ρVvapor density
σ,γsurface tension, dynes/cm or interfacial tension
dimensionless distance, Eq. (15-14a)
χterm defined in Eq. (13-49)
φc, φdvolumetric fraction of continuous and dispersed phases
φd,feedvolumetric fraction of dispersed phase in feed
φliquid phase packing parameter, Eq. (16-38)
φBsolvent interaction parameter, Eq. (15-23b)
φdcrelative froth density in downcomer, Eq. (10-29)
φeeffective relative froth density, Eq. (16-109d)
ψρwaterL, Chapter 10
ψe/(e + L), fractional entrainment, Chapter 10
ψpacking parameter for gas phase, Eq. (16-37)
ΩDcollision integral, Table 15-2
μC μDviscosity of continuous and dispersed phases, Pa·s
μH μLviscosity of heavy and light phases, Pa·s
μmmixture viscosity, Eq. (13-55), Pa·s
ρC, ρDdensities of continuous and dispersed phases, g/m3
ρmmixture density, Eq. (13-53), g/m3
ρmmolar density, mol/m3
ωrevolutions per second


Chapter 17

a, ajterm in quadratic equations for well-mixed membrane systems, Eqs. (17-10b), (17-74a), and
âconstant in expression to calculate osmotic pressure, kPa/mole fraction, Eq. (17-15a)
aconstant in expression to calculate osmotic pressure, kPa/weight fraction, Eq. (17-15b)
aiactivities, Eq. (17-51)
Amembrane area available for mass transfer, cm2 or m2
b, bjterm in quadratic equations for well-mixed membrane systems, Eqs. (17-10c), (17-74b), and
c, cjterm in quadratic equations for well-mixed membrane systems, Eqs. (17-10d), (17-74c) and
cconcentration, g solute/L solution
coutoutlet concentration of solute, g/L
cppermeate concentration of solute, g/L
cwconcentration of solute at wall, g/L
cwater concentration in permeate in Figure 17-17
CPL,pliquid heat capacity of permeate, kJ/(kg °C)
CPV,pvapor heat capacity of permeate, kJ/(kg °C)
dtdiameter of tube, cm
dtanktank diameter, cm
Ddiffusivity in solution, cm2/s
Dmdiffusivity in the membrane, cm2/s
Fpvolumetric flow rate of permeate, cm3/s
Foutvolumetric flow rate of exiting retentate, cm3/s
Fsolvvolumetric flow rate of solvent in RO, cm3/s
molar flow rate, mol/s, mol/min, etc.
F′mass flow rate, g/s, g/min, kg/min, etc.
h½ distance between parallel plates, cm
hinenthalpy of inlet liquid stream in pervaporation, kJ/kg
houtenthalpy of outlet liquid retentate stream in pervaporation, kJ/kg
HAsolubility parameter, cc(STP)/[cm3 (cm Hg)]
Hpenthalpy of vapor permeate stream in pervaporation, kJ/kg
kmass transfer coefficient, typically cm/s, Eq. (17-33)
K′solvpermeability of the solvent through membrane, L/(atm m2 day) or similar units
jcounter for stage location in staged models in Figure 17-19
Jvolumetric flux, cm3/(s cm2) or m3/(m2 day), Eq. (17-1b)
Jmass flux, g/(s cm2)or g/(m2 day), Eq. (17-1c)
Ĵmole flux, mol/(s cm2) or kmol/(day m2), Eq. (17-1d)
K′Asolute permeability, g/(m s wt frac)
Km,irate transfer term for multicomponent gas permeation, dimensionless, Eq. (17-11d)
Ltube length, cm
Mconcentration polarization modulus in wt fraction units, dimensionless, Eq. (17-17)
Mcconcentration polarization modulus in concentration units, dimensionless, Eq. (17-48)
MWmolecular weight, g/mol or kg/kmol
Nnumber of well-mixed stages in models in Figure 17-19
ppressure, Pa, kPa, atm, mm Hg, etc.
pApartial pressure of species A, Pa, atm, mm Hg, etc.
pptotal pressure on the permeate (low pressure) side, Pa, kPa, atm, mm Hg, etc.
prtotal pressure on the retentate (high pressure) side, Pa, kPa, atm, mm Hg, etc.
PApermeability of species A in the membrane, cc(STP) cm/[cm2 s cm Hg]
Rrejection coefficient in wt frac units, dimensionless, Eq. (17-24a)
inherent rejection coefficient (M = 1), dimensionless
Rcrejection coefficient in conc. units, dimensionless, Eq. (17-48)
Rtube radius, cm
ReReynolds number, dimensionless, Eq. (17-35b)
ScSchmidt number, dimensionless, Eq. (17-35c)
ShSherwood number, dimensionless, Eq. (17-35a)
tmsthickness of membrane skin doing separation, μm, mm, cm, or m
Ttemperature, °C
Trefreference temperature, °C
ubbulk velocity in tube, cm/s
vsolventpartial molar volume of the solvent, cm3/gmole
xwt frac of retentate in pervaporation. In binary system refers to more permeable species.
xgwt frac at which solute gels in UF
xpwt frac solute in liquid permeate in RO and UF
xrwt frac solute in retentate in RO and UF
ywt frac of permeate in pervaporation. In binary system refers to more permeable species.
ypmole fraction solute in gas permeate for gas permeation
yrmole fraction solute in gas retentate for gas permeation
yr,wmole fraction solute in gas retentate at membrane wall
yt,Amole fraction solute A in gas that transfers through the membrane


Greek letters

αselectivity, dimensionless, Gas Permeation: Eq. (17-4b), RO: Eq. (17-20), pervaporation: Eq. (17-53a)
Δxdifference in wt frac of solute across the membrane
Δπdifference in the osmotic pressure across the membrane, Pa, atm, mm Hg, etc.
πosmotic pressure, Pa, kPa, atm, mm Hg, etc.
θcut = , with flows in molar units, dimensionless
θ′cut = F′p/F′in in flows in mass units, dimensionless
μviscosity, centipoise or g/(cm s)
ν = μ/ρkinematic viscosity, cm2/s
ρsolvmass solvent density, kg/m3
solvmolar solvent density, kmol/m3
λpmass latent heat of vaporization of the permeate in pervaporation determined at the reference temperature, kJ/kg
ωstirrer speed in radians/s


Chapter 18

aconstant in Langmuir isotherm, same units as q/c, Eq. (18-6c)
aargument for error function, dimensionless, Eq. (18-70), Table 18-7
apsurface area of the particles per volume, m–1
Accross-sectional area of column, m2
Awwall surface area per volume of column for heat transfer, m–1
bconstant in Langmuir isotherm, (concentration)–1, Eq. (18-6c)
cAconcentration of species A, kg/m3, kmol/m3, g/L, etc.
ciconcentration of species i, kg/m3, kmol/m3, g/L, etc., or
ciconcentration of ion i in solution, typically equivalents/m3
concentration of species i that would be in equilibrium with , same units as ci
average concentration of solute in pore, same units as ci
cporefluid concentration at surface of adsorbent pores, same units as ci
ci,surfacefluid concentration at surface of particles, εp = 0, same units as ci
cRiconcentration of ion i on the resin, typically equivalents/m3
cRTtotal concentration of ions on the resin, typically equivalents/m3
cTtotal concentration of ions in solution, typically equivalents/m3
Ciconstant relating solute velocity to interstitial velocity, dimensionless, Eq. (18-15e)
CP,fheat capacity of the fluid, cal/(g °C), cal/(mol °C), J/(g K), etc.
CP,pheat capacity of particle including pore fluid, same units CP,f
CP,sheat capacity of the solid, same units as CP,f
CP,wheat capacity of the wall, same units as CP,f
dpparticle diameter, cm or m
Ddesorbent rate in SMB, same units as F
D/Fdesorbent to feed ratio in SMB, dimensionless
Dcolcolumn diameter, m or cm
Ddiffusivity including both molecular and Knudsen diffusivities, m2/s or cm2/s
Deffectiveeffective diffusivity, m2/s or cm2/s, Eq. (18-4)
DKKnudsen diffusivity, m2/s or cm2/s, Eq. (18-51)
Dmolecularmolecular diffusivity in free solution, m2/s or cm2/s
Dssurface diffusivity, m2/s or cm2/s, Eq. (18-53)
erferror function, Eq. (18-70) and Table 18-7
EDaxial dispersion coefficient due to both eddy and molecular effects, m2/s or cm2/s
EDTthermal axial dispersion coefficient, m2/s or cm2/s
Eeffeffective axial dispersion coefficient, same units ED, Eq. (18-68)
Fvolumetric feed rate, e.g., m3/h, cm3/min, liter/h
hpparticle heat transfer coefficient, J/(K s m2) or similar units
hwwall heat transfer coefficient, J/(K s m2) or similar units
HETPheight of equilibrium plate, cm/plate, Eq. (18-78b)
kffilm mass transfer coefficient, m/s or cm/s
km,clumped parameter mass transfer coefficient with concentration driving force, m/s or cm/s, Eqs. (18-56a) and (18-57a)
km,qlumped parameter mass transfer coefficient with amount adsorbed driving force, m/s or cm/s, Eqs. (18-56b) and (18-57b)
KABmass action equilibrium constant for monovalent-monovalent ion exchange, dimensionless, Eq. (18-40a)
KA,cadsorption equilibrium constant in terms of concentration, units are (concentration)-1
K′i,clinearized adsorption equilibrium constant in terms of concentration, units are units of q/c, Eq. (18-6b)
KAopre-exponential factor in Arrhenius Eq, (18-7a), same units as KA
KA,padsorption equilibrium constant in terms of partial pressure, units are (pressure)-1
K′A,plinearized adsorption equilibrium constant in terms of partial pressure, units are units of qA/pA, Eq. (18-5b)
Kdsize exclusion parameter, dimensionless
KDBmass action equilibrium constant for divalent-monovalent ion exchange, same units as cT/cRT, Eq. (18-41)
KDEDonnan exclusion factor, dimensionless, following Eq. (18-44)
Llength of packing in column, m or cm
LMTZlength of mass transfer zone, Figure 18-23, m or cm
Mmolecular weight of solute, g/mol or kg/kmol
Mimultipliers in Eqs. (18-29), dimensionless
Nequivalent number of plates in chromatography, Eq. (18-78)
NPePeclet number, dimensionless, Eq. (18-62)
pApartial pressure of species A, mm Hg, kPa, or other pressure units
phhigh pressure, mm Hg, kPa, or other pressure units
pLlow pressure, mm Hg, kPa, or other pressure units
PeLPeclet number based on length, dimensionless, Eq. (18-78a)
qAamount of species A adsorbed, kg/kg adsorbent, mol/kg adsorbent, or kg/L
qA,maxmaximum amount of species A that can adsorb, kg/kg adsorbent, mol/kg adsorbent, or kg/L
qFamount adsorbed in equilibrium with feed concentration, same units as qA
average amount of species i adsorbed, kg/kg adsorbent, mol/kg adsorbent, or kg/L
amount adsorbed that would be in equilibrium with fluid of concentration ci, same units as qA
Qvolumetric flow rate, m3/s, L/min, etc.
rppore radius, m or cm
Rresolution, dimensionless, Eq. (18-82)
Rgas constant (e.g., )
ReReynolds number, dimensionless, Eq. (18-60)
ScSchmidt number, dimensionless, Eq. (18-60)
ShSherwood number, dimensionless, Eq. (18-60)
ttime, s, min, or h
tbrbreakthrough time, s, min, or h
tcentertime center of pattern exits column, s, min, or h, Eq. (18-85b)
telutionelution time, s, min, or h
tF, tfeedfeed time, s, min, or h
tMTZtime of mass transfer zone, Figure 18-23, s, min, or h
tRretention time, s, min, or h
tswswitching time in SMB, s, min, or h
Ttemperature, °C or K
Tambambient temperature, °C or K
Tssolid temperature, °C or K
uion,ivelocity of ion i, m/s or cm/s
usaverage solute velocity, m/s or cm/s
average of solute velocities for A and B, cm/s, Eq. (18-83)
us,ion,idiffuse wave velocity of ion i, m/s or cm/s
ushshock wave velocity, m/s or cm/s
ush,ion,ishock wave velocity of ion i, m/s or cm/s
uththermal wave velocity, m/s or cm/s
utotal_ionvelocity of total ion wave, m/s or cm/s
vA,productinterstitial velocity of A Product if it was in the column, m/s or cm/s = (A Product)/(εe Ac)
vB,productinterstitial velocity of B Product if it was in the column, m/s or cm/s = (B Product)/(εe Ac)
vDinterstitial velocity of desorbent if it was in the column, m/s or cm/s = D/(εe Ac)
vFeedinterstitial velocity of feed if it was in the column, m/s or cm/s = F/(εe Ac)
vinterinterstitial velocity, m/s or cm/s, Eq. (18-2b)
vsupersuperficial velocity, m/s or cm/s, Eq. (18-2a)
Vavailablevolume available to molecule, m3, Eq. (18-1c)
Vcolumncolumn volume, m3
Vfeedvolume feed gas, m3
Vfluidvolume available to fluid, m3, Eq. (18-1a)
Vpurgevolume purge gas, m3
wA, wBwidth of chromatographic peak, s, min or hours
Wweight of the column per length, kg/m
xdeviation from the location of the peak maximum, dimensionless Eq. (18-79)
xldeviation from peak maximum in length units, Eq. (18-80b)
xtdeviation from peak maximum in time units, Eq. (18-80a)
xweight or mole fraction solute in liquid, kg solute/kg liquid or kmol solute/kmol liquid, dimensionless
xi= ci/cT equivalent fraction of ion in solution, dimensionless
Xbreakthrough (z,t)general solution for column breakthrough for linear isotherms, same units as c, Eq. (18-72)
yweight or mole fraction solute in gas, kg solute/kg gas, or kmol solute/kmol gas, dimensionless
yi= cRi/cRT equivalent fraction of ion on resin, dimensionless
zaxial distance in column, m or cm. (Measured from closed end for PSA pressure change calculations)


Greek letters

βstrongratio velocities of strong and weak solutes, Eq. (18-27), dimensionless
Δcchange in solute concentration, same units as c
ΔHadsheat of adsorption, J/kg, cal/gmole, etc.
ΔpAchange in partial pressure, kPa, atm, etc.
Δqchange in amount adsorbed, kmol/kg adsorbent, kg/kg adsorbent, kmol/m3, or kg/m3
Δtchange in time, s, min, or h
ΔTfchange in fluid temperature, °C or K
Δzincrement of column length, m
γvolumetric purge to feed ratio in PSA, dimensionless, Eq. (18-26)
εeexternal porosity, dimensionless
εpinternal or pore porosity, dimensionless
εTtotal porosity, dimensionless, Eq. (18-1b)
ρbbulk density of adsorbent, kg/m3, Eq. (18-3b)
ρffluid density, kg/m3
molar density of fluid, kmol/m3
ρpparticle density, kg/m3, Eq. (18-3a)
ρsstructural density of solid, kg/m3
σstandard deviation of Gaussian chromatographic peak, Eq. (18-79)
σlstandard deviation in length units, m or cm, Eq. (18-80b)
σtstandard deviation in time units, min or s, Eq. (18-80a)
τtortuosity, dimensionless, Eq. (18-4)
ζGreek letter zeta used as dummy variable in Eq. (18-70)