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Kwang W. Won ∗ , Arnie R. Smith, Gerald A. Zeininger

Fluor Enterprises Inc., 3 Polaris Way, Aliso Viejo, CA 92698, USA

Received 9 November 2005; received in revised form 30 December 2005; accepted 31 December 2005

Abstract

The design of fire relief systems for petroleum refineries, petrochemical, chemical and natural gas plants requires two accurate system design

parameters: the latent heat of vaporization and sonic velocity. These design parameters further require accurate thermodynamic properties. At

present, various approximate methods and thermodynamic models are utilized to estimate the latent heat of vaporization of fluid mixtures with

varying degrees of success. Similarly, approximate methods have been used in industry to estimate the sonic velocity at which compressible fluid

mixtures can flow through relief valve orifices and discharge piping.

This paper presents the following:

1. Thermodynamically rigorous methods for the calculation of the latent heat of vaporization and the sonic velocity. These methods are applied

to typical fluid mixtures using industry-standard property models and compare the calculated results with data published in scientific literature.

2. The American Petroleum Institute (API) recommendation of the minimum value of latent heat of vaporization of hydrocarbon mixtures is too

large to accept for safe ﬁre relief system design when no accurate latent-heat value is available near the critical point. Note: recommendation

by API for minimum approximate heat of vaporization of multicomponent hydrocarbon mixtures in the absence of latent-heat data at the critical

point is 50 Btu/lb (116 kJ/kg) – see Section 3.15.3.1 of API Recommended Practice 521: “Guide for Pressure-Relieving and Depressuring

Systems, 1997”).

3. The need of accurate thermodynamic property data of ﬂuid mixtures necessary to validate the thermodynamic model at relief system operating

conditions. Currently, these types of data are scarce in the open literature because data measurements have been difficult at the temperatures

and pressure of interest.

Keywords: Fire relief system; Latent heats of vaporization; Thermodynamic method; Petroleum refinery; Natural gas processing; Sonic velocity

higher pressure

In natural gas processing, petroleum refineries, petrochem- • by the failure of a check valve to close resulting in a reversal

ical and chemical plants, pressure vessels, heat exchangers, of the fluid flow

pumps, compressors and piping systems are designed to operate • by heat-exchanger tube failure

within the normal operating conditions between the minimum • by reflux failure

and maximum temperatures and pressures. However, overpres- • by the utility failures including electric, cooling water and

sures exceeding the maximum pressure limit can develop in the instrument air

following events: • by plant fires

• by inadvertent closure of a block valve on the outlet of pres- Fires external to pressure vessels increase the temperature

sure vessel while the plant is on stream of fluid content due to the abnormal heat input. The increase

of temperature results in the operating pressure exceeding the

design pressure intended for the fire relief valve. When the fluid

∗ Corresponding author. Tel.: +1 949 349 5312; fax: +1 949 349 2914. inside the vessel contains both liquid and gas, the rate of gas flow

E-mail address: ray.won@fluor.com (K.W. Won). through the relief valve is approximately equal to the rate of heat

0378-3812/$ – see front matter © 2006 Elsevier B.V. All rights reserved.

doi:10.1016/j.fluid.2005.12.045

42 K.W. Won et al. / Fluid Phase Equilibria 241 (2006) 41–50

mixture. The maximum velocity of the gas discharge will be the

sonic velocity, which is dependent on the temperature, pressure

and properties of the fluid. Therefore, the accurate design of

the pressure relief system capacity requires accurate estimation

of the latent heat of vaporization and sonic velocity of fluid

mixtures, which requires thermodynamic property data at high

temperatures.

In the past several decades, latent heats of vaporization have

been extensively measured and published for pure fluids and

simple fluid mixtures. At the same time, several thermodynamic

models have been applied successfully to the phase equilibrium

and enthalpy calculations for mixtures consisting of hydrocar-

bons and slightly polar components of relatively small molecular

sizes at low to moderate temperature ranges. However, much less

attention has been paid to the properties of fluid mixtures consist-

ing of molecules with much different molecular sizes including

petroleum fractions. As a consequence, accurate latent heats Fig. 1. Rigorous thermodynamic calculation method of latent heat of vaporiza-

tion of fluid mixtures.

of vaporization and property data needed for the calculation of

sonic velocity for such fluid mixtures are scarce.

Even when the total enthalpy data have been published for

such fluid mixtures, the vapor–liquid equilibrium data of the Method 2 uses a non-rigorous estimate of the latent heat of vapor-

system have not been published at the similar conditions. As a ization as follows:

result, when the total enthalpies calculated by thermodynamic λv = Hv − HL (2)

models do not agree with data within the accuracy acceptable for

engineering design purposes, it is difficult to determine which where Hv and HL are the specific enthalpy of the vapor and liquid

source is the cause of the disagreement. This paper points out at equilibrium. The above two equations are valid only for pure

some important areas where new thermodynamic data are nec- fluid. If these equations were used for mixtures, substantial error

essary. would result because the concentrations of vapor and liquid at

equilibrium could be very different.

This paper proposes a new thermodynamically rigorous

2. Methods of latent heat of vaporization

method 3, based on a thermodynamic cycle depicted in Fig. 1.

Step A is the isothermal compression of the liquid mixture above

The latent heat of vaporization required for the fire relief load

the pressure set by the fire relief valve by a small P, say 7 kPa

calculation is commonly calculated by an energy balance [27]

(1 psia). Step B is an isobaric heating of the compressed fluid to

simulating a fire relief scenario (method 1), where the liquid at its

a higher temperature, or its boiling-point temperature. Step C is

boiling point temperature in a vessel is heated and is vaporized.

an isothermal vaporization step where the compressed fluid is

As the temperature continues to increase, the equilibrium pres-

expanded to the original set pressure. The latent heat of vapor-

sure of the fluid mixture increases until it reaches and exceeds

ization is the net heat effect of path a–b and path c–d divided by

the set pressure of the fire relief valve, resulting in the venting

the amount of vapor generated in path c–d. The heat required

or relief of the vapor. The latent heat of vaporization, λ, can be

for path b-c is the sensible heat, which is not a part of the latent

estimated by an incremental flash from T to T + T, where P is

heat of vaporization. This can be summarized by the following

constant at relief conditions:

formula:

1 Cp,F + Cp,L Cp,F + Cp,v Qa + Qc

λv = Q − WL T − Wv T λv = (3)

Wv 2 2 Wv

(1)

For a pure fluid, Eq. (3) reduces to Eq. (1a) if we set both P

where T is equal to the bubble point temperature, Q the heat and Qa equal to zero. Qc /Wv is a constant equal to the latent heat

input, WL and Wv are the weights of liquid and vapor, Cp the of vaporization.

isobaric heat capacity and T is the temperature difference. Eqs. (1) and (2) and the thermodynamically rigorous method,

For a pure fluid, there is no temperature change during the Eq. (3), are used to calculate the latent heat of vaporization of

flash vaporization and the latent heat equation reduces to a sim- fluid mixtures. In order to investigate the differences of the

ple equation, which is the flash duty divided by the generated three methods, each has been applied to five sets of typical

vapor mass as follows: mixtures and the results are presented in Tables 1 and 2. In

these calculations, the initial 5% by weight of the low boiling,

Q light components were vaporized and removed from the system

λv = (1a)

Wv because the light ends, including air, would misrepresent the

K.W. Won et al. / Fluid Phase Equilibria 241 (2006) 41–50 43

Table 1

Latent heat of vaporization of C3 and nC4 binary mixtures (kJ/kg)

Thermodynamic methods Model 791a 2170a 3549a

5%b 10%b 50%b 90%b 5%b 10%b 50%b 90%b 5%b 10%b 50%b 90%b

Method 1 HYSYS, PR 314 316 335 347 216 216 235 251 84 88 116 137

PRO/II, PR 316 319 335 349 216 219 237 251 86 91 119 137

Method 2 HYSYS, PR 307 300 288 333 214 212 212 242 88 93 119 137

PRO/II, PR 316 319 335 347 219 226 244 254 91 100 137 144

Method 3 PRO/II, PR 314 316 333 347 215 217 232 249 84 87 114 135

a System pressure (kPa).

b mol% C3 in the binary liquid mixture.

latent heat of the fluid mixture. The remaining portion is at its a binary mixture consisting of methane-normal C10 , which rep-

boiling point temperature at this pressure. resents a mixture in which the constituent’s molecular sizes are

Table 1 presents the latent heats of vaporization of five very much different. The concentrations of multi-component

propane-n butane binary mixtures calculated by the three meth- C3 –C12 mixture, light hydrocarbons and petroleum fractions,

ods at three pressure levels by Peng-Robinson [25] equation of and methane-normal C10 binary mixture are provided in sep-

state (PR) in HYSYS (version 3.2, Hyprotech Inc.) and PRO/II arate tables. It is noteworthy that the differences between the

(version 7.0, Simulation Science Inc.). For method 3, the latent results of method 1 and 2 are substantial for mixtures consisting

heats of vaporization and the boiling point temperatures calcu- of small and large molecules at high pressures including low

lated only by PR model in PRO/II are presented. The results in sulfur diesel and light hydrocarbon mixtures at 2171 kPa and

Table 1 indicate that the latent heats of vaporization calculated methane-normal C10 mixtures at 1136 kPa.

by the energy balance agree with the values of method 3 within In general, the results of method 1 and 3 are in agreement.

about 2% or 3.5 kJ/kg. On the other hand, the difference between The latent heat of vaporization of the mixture consisting of light

methods 2 and 3 is appreciably larger with about 7% or 13. kJ/kg hydrocarbons and Low Sulfur Diesel (LSR) calculated by meth-

of root mean squared deviations. ods 1 and 3 at 2171 kPa ranges from 35 to 37 kJ/kg. These values

Table 2 presents the latent heats of vaporization of four are substantially smaller than 116.3 kJ/kg, the minimum value

multi-component systems including a petroleum fraction and recommended by API (American Petroleum Institute).

Table 2

Latent heat of vaporization of multi-component system (kJ/kg)

Thermodynamic methods Model C3–C12a LSR diesela Diesel + light HCa C1–C10a

PRO/II, PR 256 116 165 179 37 158

Method 2 HYSYS, PR 156 105 170 177 67 −251

PRO/II, PR 261 142 177 219 74 188

Method 3 PRO/II, PR 242 123 165 172 34 163

Temperature (K) PRO/II, PR 450 529 641 610 710 525

Mixture C3–C12

Comp C3 nC12 nC5 nC6 nC7 nC8 nC9 nC10 nC11 nC12

mol% 2 3 8 15 22 22 15 8 3 2

LSR diesel

TBP (F) 242 391 423 483 519 552 595 617 645

Comp nC5 nC6 nC7 nC8 CH4 nC10 LSR diesel Light HC

mol% 10 20 30 40 10 90 95 5

a Multi-component system

b System pressure (kPa).

44 K.W. Won et al. / Fluid Phase Equilibria 241 (2006) 41–50

vaporization leads to under design of the pressure relief system,

which is not safe. Also, the heat of vaporization for methane and

normal C10 , which was calculated by method 2 at 1136 kPa, is

negative, which is meaningless.

The PR model in Aspen Plus (version 12.1, Aspen Technol-

ogy Inc.) provides essentially the same results for method 3 as

the PR model in PRO/II. The results of Aspen Plus were not

shown in Tables 1 and 2.

fire relief design are unavailable to the best knowledge of the

authors. However, most of the experimental enthalpy data of

partially vaporized mixtures have been measured without chem-

ical analysis of the vapor and liquid at equilibrium. Therefore,

the exact calculation of the latent heat of vaporization from the

published total enthalpy data with an isobaric calorimeter is not

possible.

Extensive enthalpy data of pure components and fluid mix-

tures have been compiled and published by Daubert [1–4] in the

Research Reports (RR) of Gas Processors Association (GPA).

In the GPA RR-81, Daubert [5] presents the evaluation of

Peng-Robinson Computer Program with the GPA Data Bank

of Selected Enthalpy Values.

The RR-81 shows appreciable arithmetic average (AA) and

root-mean-squared (rms) deviations between the enthalpy data

and those calculated by the PR equation of state. Additional Fig. 2. (a) Isobaric enthalpy at 1379 kPa of a binary mixture: 21.8 mol% nC5

enthalpy data have been published for single fluid by Eubank et and 78.2 mol% nC8. (b) Isobaric enthalpy at 2759 kPa of a binary mixture:

al. [6] and for methane binary mixtures by Wilson [7]. 21.8 mol% nC5 and 78.2 mol% nC8.

4. Comparison of enthalpy calculation results with data the curve representing the isobaric enthalpy as a function of tem-

perature. The temperature at which the slope starts to increase, at

This work uses the Peng-Robinson equation of state for ther- approximately 494 K, is the bubble point temperature. The tem-

modynamic property calculations, because the PR model has perature at which the slope returns to linearity, at about 512 K,

been widely accepted in industry and extensively used by prac- is the dew point temperature. The similar result of the same

ticing process design engineers. In order to verify the accuracy mixture at 2758 kPa is shown in Fig. 2(b).

of the PR model, this work uses the PR model available in Aspen Both Fig. 2(a) and (b) for the n-pentane and n-octane sys-

Plus to calculate the enthalpies of fluid mixtures at the condi- tem indicate that both the PR and PR-LK models seem to agree

tions of experimental measurements. Aspen Plus was selected with each other and predicts the isobaric total enthalpy of the

for this study because it offers an expedient table generation mixture within approximately 12. kJ/kg. However, one enthalpy

capability of isobaric enthalpy versus temperature. At each iso- data point of a partially vaporized mixture at 1379 kPa and

bar, the enthalpy data of the mixtures were calculated relative to 499.8 K was appreciably underestimated by both models. Table 3

that at 297.04 K. It is necessary to use one standard state tem- presents the average bias and root mean squared deviations in

perature for the comparison purpose, even if it is different from kJ/kg for liquid, gas and two-phase regions.

that of the published experimental data. Fig. 3(a) presents the enthalpy data of a binary sys-

Fig. 2(a) presents the enthalpy data of a binary mixture tem consisting of 32.2 mol% n-pentane and 67.8 mol% trans-

consisting of 21.8 mol% n-pentane and 78.2 mol% n-octane at Decahydronaphthalene (t-Decalin) at 138 kPa between 297 and

1379 kPa as a function of temperature between 297 and 588.7 K 522 K published by Lenoir et al. [10] and Fig. 3(b) presents the

[8]. Origin of the figure shows that the relative enthalpy of the liq- similar result at 690 kPa between 297 and 588.7 K. Fig. 3(a) and

uid mixture is zero at 297 K. The bold line is the result calculated (b) indicate that enthalpies of both liquid and gas phases were

by the Peng-Robinson equation of state in Aspen Plus. The reg- better predicted by the PR-LK model, but the enthalpy of the

ular line is the result of PR-LK, in which the phase equilibrium partially vaporized mixture at 138 kPa and 455.4 K was substan-

was calculated by the PR model, but the volumetric properties tially overestimated by both models. The prediction error will

and enthalpies were calculated by the Lee-Kesler model [9]. result in the overestimation of the latent heat of vaporization of

Vaporization is responsible for the sharp increase of the slope of this type of mixture, which would lead to the underestimated

K.W. Won et al. / Fluid Phase Equilibria 241 (2006) 41–50 45

Table 3 Table 3a

Arithmetic and RMSD (kJ/kg) of ASPEN Plus PR and PR-LK models from Arithmetic and RMSD (kJ/kg) of ASPEN Plus PR and PR-LK models from

Isobaric Enthalpy Data of 21.8 mol% nC5 in nC8 [8] Isobaric Enthalpy Data of 32.2 mol% nC5 in t-Decalin [10]

P = 1379 kPaa P = 2759 kPaa P = 138 kPaa P = 689 kPaa

arithc RMSDc arithc RMSDc arithc RMSDc arithc RMSDc arithc RMSDc arith RMSDc arithc RMSDc arithc RMSDc

Liquid 7.3 7.6 0.0 2.6 2.6 6.7 0.7 3.0 L 5.2 5.9 0.3 0.7 12 14 −0.4 0.8

Gas −4.6 4.8 −11 10 −8.8 8.8 −14 14 G 21 21 −5.0 5.2 20 21 −5.2 7.1

2 phase 48 46 −10 10 −12 12 2 phase −5.5 21 −20 33 17 17 −2.6 2.8

Total 5.0 14.7 −1.6 14.6 −1.1 8.0 −3.4 7.5 Total 10 18 −7.3 17 17 18 −3.1 4.6

a System a System

b Model b Model

c Dev (kJ/kg) c Dev (kJ/kg)

fire relief system design. Figs. 2(b) and 3(b) show that at higher PR-LK, Simulation Sciences Inc. PR and modified PR (PRM),

pressures, the enthalpies of both mixtures were better predicted SRK [26] and modified SRK (SRKM) appreciably overestimate

by the PR-LK model than the PR model alone. Table 3a presents the enthalpies of partially vaporized mixtures. It is important to

the average bias and root mean squared deviations of Aspen PR note that the overestimated isobaric total enthalpies of the par-

and PR-LK models from the data. tially vaporized mixtures will lead to under designed fire relief

Fig. 4(a) and (b) compare the calculated enthalpies with systems. However, it is not possible to calculate the latent heats

data for the binary mixture containing 16.7 mol% n-pentane and of vaporization from the total isobaric enthalpy data or to dif-

83.3 mol% n-Hexadecane at 172 and 276 kPa bar between 297 ferentiate the cause of disagreement between the data and the

and 599.8 K. This mixture consists of molecules with very dif- models.

ferent sizes and, therefore, all the models including Aspen PR,

Fig. 3. (a) Isobaric enthalpy at 138 kPa of a binary mixture: 32.2 mol% nC5 and Fig. 4. (a) Isobaric enthalpy at 172 kPa of a binary mixture: 16.7 mol% nC5

67.8 mol% trans-Decalin. (b) Isobaric enthalpy at 690 kPa of a binary mixture: and 83.3 mol% nC16. (b) Isobaric enthalpy at 276 kPa of a binary mixture:

32.2 mol% nC5 and 67.8 mol% trans-Decalin. 16.7 mol% nC5 and 83.3 mol% nC16.

46 K.W. Won et al. / Fluid Phase Equilibria 241 (2006) 41–50

Table 3b Table 4

Arithmetic and RMSD (kJ/kg) of SSI PR and PRM models from Isobaric Infinite dilution activity coefficient data and sources

Enthalpy Data of 16.7 mol% nC5 in nC16 [20]

Temp (K) Solute Solvent Act coeff Data source

P = 172 kPaa P = 276 kPaa

293.2 nC5 nC8 0.97 Thomas et al. [21]

PRb PRMb PRb PRMb 328.2 nC5 nC8 1.07 Arnold et al. [22]

348.2 nC5 nC8 1.06 Arnold et al. [22]

arithc RMSDc arithc RMSDc arithc RMSDc arithc RMSDc

388.2 nC5 nC8 1.04 Arnold et al. [22]

L 5.8 6.7 −27 30 9.0 11 −33 35 298.2 nC5 nC16 0.926 Kikic and Renon [12]

298.2 nC5 nC16 0.825 Richon et al. [13]

G 8.1 8.1 −50 50 313.2 nC5 nC16 0.87 Snyder and Thomas [11]

2 phase −1.6 29 −59 66 9.0 26 −53 57 343.2 nC5 nC16 0.859 Snyder and Thomas [11]

363.2 nC5 nC16 0.852 Snyder and Thomas [11]

Total 0.6 25 −52 60 9.0 21 −45 50 298.2 nC6 nC16 0.892 Lenoir [14]

a System 273.2 nC6 nC16 0.904 Letcher and Netherton [15]

b Model 298.2 nC6 nC16 0.892 Lenoir [14]

c Dev (kJ/kg) 313.2 nC6 nC16 0.892 Snyder and Thomas [11]

343.2 nC6 nC16 0.882 Snyder and Thomas [11]

363.2 nC6 nC16 0.876 Snyder and Thomas [11]

298.2 nC6 Decalin 1.26 Monfort et al. [23]

Table 3b presents average bias and root mean squared devia- 298.2 nC6 Decalin 1.264 Lerol et al. [24]

300 nC4 nC16 1.107 Chappelow and Prausnitz [28]

tions of the isobaric enthalpies, which were calculated by SSI PR

325 nC4 nC16 0.919 Chappelow and Prausnitz [28]

and PRM models from the data. The SSI PR model predicts the 350 nC4 nC16 0.905 Chappelow and Prausnitz [28]

isobaric enthalpies of the gas and liquid mixtures within about 375 nC4 nC16 0.881 Chappelow and Prausnitz [28]

9.3 kJ/kg at 172 and 276 kPa. However, the enthalpies of the 400 nC4 nC16 0.86 Chappelow and Prausnitz [28]

two-phase region are overestimated by more than 23 kJ/kg. At 425 nC4 nC16 0.844 Chappelow and Prausnitz [28]

450 nC4 nC16 0.823 Chappelow and Prausnitz [28]

276 kPa, the experimental data shows that the mixture has two

475 nC4 nC16 0.793 Chappelow and Prausnitz [28]

phases at the maximum experimental temperature. Therefore,

all the data above the bubble point temperature were assumed to

be partially vaporized. The PRM model overestimates the liquid

heat capacity and the vapor fraction in the partially vaporized 5. Vapor–liquid equilibrium data of mixtures consisting

region, relative to the PR model. As a result of the overestima- of large and small molecules

tions, the isobaric enthalpies of liquids, gases, and the two-phase

region are overestimated by more than 23, 46 and more than The appreciable differences of the experimental and calcu-

58 kJ/kg, respectively. Table 3c presents the similar results cal- lated enthalpies of the partially vaporized mixtures necessitate

culated by SSI SRK and modified SRK (SRKM) models. the examination of the vapor–liquid equilibrium data of the

Either the overestimated vapor–liquid equilibrium K values mixtures around the experimental condition. The vapor liquid

or the overestimated latent heats of vaporization can lead to the equilibrium data of the n-pentane and n-hexadecane binary sys-

overestimated isobaric total enthalpies of the partially vaporized tem were published only for an infinitely dilute system with

mixtures. Therefore, the accuracy of the PR model was investi- respect to n-pentane as an infinite dilution activity coefficient

gated by comparing the calculated vapor–liquid equilibrium K (γ ∞ ) between 313.2 and 363.2 K by Snyder and Thomas [11],

value of smaller molecules in normal hexadecane at the temper- at 298.2 K by Kikic and Renon [12] and by Richon et al. [13].

ature range of interest. Similar data for the related systems were published by Chap-

pelow and Prausnitz [28] as the Henry’s coefficient (Hc ) for

n-butane in n-hexadecane system between 300 and 475 K. The

Table 3c γ ∞ data of n-hexane in n-hexadecane have been published by

Arithmetic and RMSD (kJ/kg) of SSI SRK and SRKM models from Isobaric Snyder and Thomas between 313.2 and 363.2 K, by Lenoir [14]

Enthalpy Data of 16.7 mol% nC5 in nC16 [20] at 298.2 K and by Letcher and Netherton [15] at 273.2 K.

P = 172 kPaa P = 276 kPaa Chappelow and Prausnitz reported Henry’s coefficient data of

n-butane in n-hexadecane, while all the others reported only infi-

SRKb SRKMb SRKb SRKMb

nite dilution activity coefficients. In order to make a consistent

arithc RMSDc arithc RMSDc arithc RMSDc arithc RMSDc comparison, infinite dilution activity coefficients of n-butane in

L 2.3 2.8 −30 33 3.6 5.6 −37 39 n-hexadecane were calculated from the Henry’s coefficient data

G −3.5 3.5 −56 56

by dividing them by the product of the saturated fugacity of

n-butane and Poynting correction. At the temperatures above

2 phase −12 32 −64 71 −5.2 25 −58 62

the critical temperature of n-butane, 408.2 K, the product of

Total −8.3 28 −57 64 −1.8 20 −50 54 the saturated fugacity and Poynting correction of n-butane were

a System extrapolated. This extrapolation of the fugacity of hypotheti-

b Model cal liquid above its critical temperature is similar to the work of

c Dev (kJ/kg) Prausnitz and Shair [16]. Table 4 presents the data sources of the

K.W. Won et al. / Fluid Phase Equilibria 241 (2006) 41–50 47

Fig. 6. Effect of nC5 concentration on the bubble and dew point temperatures

Fig. 5. Activity coefficients of normal nC4, nC5 and nC6 in nC16 at infinite of nC5 and nC16 binary mixture.

dilution.

infinite dilution activity coefficients and Henry’s coefficients in for the PR model, the agreement between the values calculated

n-hexadecane. by the PR model and the values derived data is excellent. For

Fig. 5 shows that the infinite dilution activity coefficient (␥∞ ) comparison purposes, the infinite dilute activity coefficient cal-

of all three light hydrocarbons in n-hexadecane are less than culated by the PR model without the binary parameter (or with

unity. One data point at the lowest temperature of the measure- the binary parameter set to zero) is also shown in Fig. 5 as a

ment is larger than one. This is not surprising, because the first broken line.

data point at the lowest (or highest) temperature is sometimes Experimental bubble and dew point temperatures for

subject to substantial uncertainty. For this type of mixtures, a the binary mixture consisting of 16.7 mol% n-pentane and

thermal solution model [17] is applicable, which predicts that 83.3 mol% n-hexadecane at 172 kPa are 407.9 and 588.4 K,

the activity coefficients of smaller molecules in larger molecules respectively. The bubble and dew point calculated by the SSI PR

of the similar type will be less than unity. Fig. 5 also shows the model with the binary coefficients are 409.8 and 575.4 K, while

infinite dilution activity coefficients of n-butane in n-hexadecane the PR model without the binary coefficient predicts 419.3 and

calculated by the PR model using the temperature-dependent 575.4 K. The binary coefficient clearly improved the accuracy of

binary coefficient (kij ) between n-butane and n-hexadecane. bubble point temperature within 1.9 K from about 11.4 K devia-

Although the Henry’s coefficient data were used to derive a lin- tions, but the dew point temperature calculation was essentially

early temperature-dependent binary interaction parameter (kij ) not affected by the binary coefficient. Fig. 6 shows the experi-

Table 5

Sonic velocity of C3 and nC4 binary gas mixtures (m/s)

System pressure (kPa)

5%a 10%a 50%a 90%a 5%a 10%a 50%a 90%a 5%a 10%a 50%a 90%a

Temperature (K) 338.2 334.4 310.4 294.3 388.0 384.0 358.7 338.4 418.0 415.0 388.2 365.0

mol% C3 in the vapor at equilibrium 11.9 22.6 74.4 96.5 8.35 16.4 65.8 94.8 6.1 12.1 58.2 92.9

Sonicvelocity(m/s)

Real gas 198 201 214 217 165 168 185 190 132 144 151 159

Ideal gas 232 235 246 249 247 249 258 264 255 256 265 273

a mol% C3 in liquid

Table 5a

Sonic velocity of multi-component gas mixtures (m/s)

Multi-component system

Temperature (K) 453 528 626 594 703 500

Sonic velocity (m/s)

Real gas 182 133 144 160 94 258

Ideal gas 214 217 180 191 185 273

48 K.W. Won et al. / Fluid Phase Equilibria 241 (2006) 41–50

mental bubble and dew points for the mixture at 172 kPa, which

3550.0

1.83

4600.0

154

147

165

80

the dew point temperature of the binary mixture is higher than

that of pure n-hexadecane at the same pressure. The maximum

1.54

4400.0

3520.0

132

150

86

136

expected. It is likely that the fluid mixture inside the calorimeter

was not at equilibrium during the partial vaporization step. Fig. 4

1.37

4200.0

shows that the binary coefficient does not improve the isobaric

130

139

95

3480.0

139

1.36

4000.0

139

141

102

6. Sonic velocity

3450.0

141

1.37

3800.0

148

148

108

area. The valve discharge area is determined such that the flow

of gases or vapors must not exceed the sonic velocity of the

3100.0

161

1.42

3400.0

165

163

116

mixture.

2760.0

177

1.51

∂P

2600.0

Vs 2 =

193

189

128

(4)

∂ρ s

where ρ is equal to the molecular weight divided by the molar

2410.0

1.57

2000.0

190

210

206

134

and thermal properties of fluids as in Eq. (4a).

Cp ∂P

1.62

1400.0

1720.0

Vs 2 = −V 2 (4a)

225

222

139

212

Cv ∂V T

Noting that Cp is simply (∂H/∂T)P, the ratio of Cp to Cv can be

1.65

1000.0

234

231

142

1030.0

231

Cp Cp

Effect of pressure on the sonic velocity of C3 and nC4 binary gas mixtures, m/s

= (4b)

Cp Cp +T (∂V/∂T )2p

1.66

(∂V/∂P)T

600.0

241

240

145

340.0

248

1.68

300.0

246

247

147

100.0

254

1.69

C3 in the binary mixture: 12.1 mol% at 415 K

100.0

250

251

148

always smaller than those of ideal gases at the same concentra-

10.0

tion and temperature and that the sonic velocities of real gases

256

1.69

10.0

252

253

149

were calculated by the numerical differentiation, agree well with

Pure iso butane at 420 K

System pressure (kPa)

Data (NBS, 1982)

Aspen PR

Crosby [19]

Data/Crosby

Sonic velocity (m/s)

Tables 5, 5a, and 5b are those of Aspen plus. Table 5b presents the

sonic velocities of a binary gas mixture consisting of 12.1 mol%

Real gas

Table 5b

vapor, which is in equilibrium with a binary liquid mixture

K.W. Won et al. / Fluid Phase Equilibria 241 (2006) 41–50 49

pressures for fluid mixtures. Further, the third term of the right-

hand side of Eq. (1) is not meaningful. Therefore, there appears

no advantage of using the approximate energy balance method.

The paper does not recommend the simple difference-in-

enthalpy method, because this method leads to appreciable error

for the systems consisting of large and small molecules.

Current Peng-Robinson equation of state appears to overes-

timate the enthalpies of partially vaporized mixtures consisting

of small and large molecules. This would lead to under designed

pressure relief system. This paper stresses the need of accurate

latent heats of vaporization data at fire relief conditions to val-

idate the accuracy of Peng-Robinson equation of state or other

thermodynamic models.

Thermodynamically rigorous method of sonic velocity cal-

Fig. 7. Effect of pressure on the velocity of sound.

culation requires more fundamental thermodynamic data than

current empirical methods, but the use of computer calculations

and the availability of reliable thermodynamic models allow

containing 10 mol% C3 and 90 mol% nC4 at 3449 kPa. For com- the thermodynamic method practical for complex mixtures at

parison, Fig. 7 also presents the sonic velocity of pure iso-butane high pressures. Even though the accuracy of the thermodynamic

(iC4) at 420 K as a function of pressure and the values published model for the calculation of sonic velocity appears adequate in

in NBS Technical Note 1051 entitled “Thermo-physical Prop- most cases investigated in this paper, the property calculations

erties of iso-butane from 114 to 700 K at Pressures to 70 MPa” of PR model are subject to appreciable error at high temper-

[18]. atures and high pressures approaching the critical state of the

The results in Fig. 7 indicate that the sonic velocity calculated fluid mixtures.

by PR model at 420 K is accurate up to about 4000 kPa bar, but

the PR model overestimates the sonic velocity above this pres-

sure. The minimum sonic velocity occurs near the critical state of List of symbols

the fluid, where the isothermal compressibility increases sharply Cp isobaric heat capacity (kJ/kg/K)

and goes through a maximum. As a result, the sonic velocity goes Cv isochoric heat capacity (kJ/kg/K)

through the minimum. The overestimated sonic velocity by PR H enthalpy (kJ/kg)

model may lead to under design of the orifice opening of the Hc (i, j) Henry’s coefficient of component i in solvent j (kPa/mol

pressure relief system. In industry, empirical design methods fraction)

are commonly practiced based on ASME Section 8, UG125- P absolute pressure (kPa)

137 or API recommended Practice 520, “Sizing, Selection, and Q heat (kJ)

Installation of Pressure-Relieving Devices in Refineries”, part T absolute temperature (K)

1-Sizing and Selection. V molar volume, m3 (kg-mol)

Fig. 7 presents the maximum iC4 gas velocity through the Vs sonic velocity (m/s)

orifice of the pressure relief valve, which was calculated by the W weight (kg)

formula of Crosby Pressure Relief Valve Engineering Handbook

[19]. It is important to note that the maximum design gas velocity Greek symbols

is substantially smaller than the sonic velocity of the bulk fluid. γ∞ infinite dilution activity coefficient

The ratio of the design gas velocity to the sonic velocity at the λv latent heat of vaporization (kJ/kg)

same temperature increases with pressure from about 65% at

about 2000 kPa to about 73% at about 4000 kPa for pure iC4.

This ratio represents the coefficient of discharge, which has been Subscript

established for a specific type of orifice by actual test with steam p isobaric condition

and some standard type of gases. s isentropic condition

T isothermal condition

v isochoric condition

7. Conclusion

ods for the calculations of the latent heats of vaporization and

sonic velocities of fluid mixtures. The authors are grateful to the management of Fluor Enter-

The approximate energy balance method appears adequate prises Inc. for permission to present this paper and to our

for the majority of cases investigated in this paper, but this colleagues, especially Garry Jacobs, Paul Mathias and Jack

method needs additional property data for sensible heat effect. Reisdorf for helpful criticisms and discussions, An Mai for the

The additional heat capacity data are seldom available at high pertinent data and Zachary Working for editorial assistance.

50 K.W. Won et al. / Fluid Phase Equilibria 241 (2006) 41–50

References inert gas stripping, Ind. Eng. Chem. Process Des. Dev. 19 (1980) 144–

147.

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and Equilibria Values, Research Report-64, Gas Processors Association, [15] T.M. Letcher, G. Netherton, J. Chem. Thermodyn. 7 (1975) 353.

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[5] T.E. Daubert, Evaluation of Peng-Robinson Computer Program with Gage Company, 1986.

GPA Data Bank of Selected Enthalpy Values, Research Report-81, Gas [20] J.M. Lenoir, H.G. Hipkin, Enthalpy of mixtures of n-hexadecane and

Processors Association, 1984. n-pentane, Fluid Phase Equilibria 15 (1970) 368–371.

[6] P.T. Eubank, K.R. Hall, J.C. Holste, M.G. Johnson, Experimental [21] E.R. Thomas, B.A. Newman, T.C. Long, D.A. Wood, C.A. Eckert, Lim-

Enthalpies of Pentanes-Plus Fractions, Research Report-121, Gas Pro- iting activity coefficients of non polar and polar solutes in both volatile

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[9] B.I. Lee, M.G. Kesler, AIChE J. 21 (1975) 510. measurement of activity coefficients at infinite dilution by iner gas strip-

[10] J.M. Lenoir, K.E. Hayworth, H.G. Hipkin, Enthalpies of Decalins and ping and gas chromatography, Ind. Eng. Chem. Process Des. Dev. 16

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