Binary Distillation - che.utah.edusutherland/3603Notes/BinaryDistillation.pdf · Batch Distillation...

17
Binary Distillation SHR Chapter 7 1 BinaryDistillation.key - March 28, 2014

Transcript of Binary Distillation - che.utah.edusutherland/3603Notes/BinaryDistillation.pdf · Batch Distillation...

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Binary Distillation

SHR Chapter 7

1 BinaryDistillation.key - March 28, 2014

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IntroductionDates back to 1

st century AD

• first used in a batch mode (distillate changes in time)

Goal: separate “heavy key” (less volatile) from “light key” (more volatile) by exploiting α≠1. • for α≫1 or α≪1, this can be done very effectively

unless an azeotrope exists (where α=1). ‣ then we recover the azeotrope and the light or heavy key,

depending on which side the feed lies.

• By 16th century, multiple stages were in use to

improve separation.

By 1976, distillation accounted for nearly 3% of the US energy consumption! • mostly in petroleum refineries

Binary distillation is simplest & most well-understood. • we will limit our discussion to binary distillation

Third Law of Thermo - typically low thermodynamic efficiency.

SHR §7.1

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Design ConsiderationsOperating pressure - “knob 1” • below ambient pressure requires vacuum operation

• many things may influence choice of operating pressure ‣Thermo: azeotrope formation, α, etc.

‣Column operating temperature range (avoiding reactions, corrosion, etc.)

• most analyses do not account for pressure variation through the column

Operating temperature - “knob 2” • Reboiler & Condenser: ‣Bottoms above ambient requires additional energy input to the

reboiler

‣Distillate below ambient requires energy removal from the condenser.

• Thermodynamics: critical points of fluids

F

D

B

V

L

L

V

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Batch Distillation

Conceptually, follows the T-x-y diagram. More rigorous analysis in SHR chapter 13

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The McCabe-Thiele Graphical Method

1925 Continuous (staged) distillation

SHR §7.2

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NomenclatureSpecifications

F total (molar) feed rate

z LK mole fraction in feed

P Column operating pressure

x LK mole fraction in distillate

x LK mole fraction in bottoms

R/R reflux ratio

Feed phase condition

VLE data (y/x plot)

Type of condenser (partial/total)

Type of reboiler (partial/total)

ResultsD Distillate (molar) flow rate

B Bottoms (molar) flow rate

N minimum number of stages

R minimum reflux flow rate

V Boilup ratio

N Number of equilibrium stages

Feed stage location

Stage compositions (

• “Light Key” (LK) - more volatile component • “Heavy Key” (HK) - less volatile component

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Preliminaries

Rectifying section - like an absorber • Feed & reboiler supply vapor • Condenser supplies liquid

Stripping section - like a stripper • Feed & condenser supply liquid • Reboiler supplies vapor

FzF = xDD + xBB

F = D +B

D = F

✓zF � xB

xD � xB

◆light-key mole balance:

overall mole balance:

combine to eliminate B & solve for D:

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Rectifying Section Operating LineLight key mole balance:

relates light-key compositions in passing streams (streams on a stage are assumed to be in equilibrium)

If L and V are constant, then this is a straight line.

• Both components have equal and constant molar enthalpies of vaporization (latent heats).

• Sensible heat, CpΔT, is negligible compared to latent heat.

• Column is insulated (no heat loss on each stage).

• Column pressure is constant (thermodynamics can be done at a single pressure).

Big assumptions, but allow for simple analysis, since L and V are constant under these assumptions.

The “McCabe-Thiele Assumptions”

L

V=

L

L+D=

L/DL/D + D/D

=R

R+ 1D

V=

1

R+ 1

Overall mole balance: V = L+D

y =

✓R

R+ 1

◆x+

✓1

R+ 1

◆xD

R ⌘ L

Dreflux ratio

operating li

ne

SHR §7.2.1

V yn+1 = Lxn +DxD

yn+1 =L

V

xn +D

V

xD

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Range of Reflux Ratiosy =

L

V

x+D

V

xD

0 ✓L

V=

R

R+ 1

◆ 1 because 0 R 1

• What happens at R = 0?

• What happens at R = ∞?

What is the minimum R that allows separation? (We will answer this question shortly)

R =L

D

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relates light-key compositions in passing streams (streams on a stage are assumed to be in equilibrium)

Stripping Section Operating Line

Light key mole balance:

Overall mole balance:

Lxm = V ym+1 +BxBMcCabe-Thiele assumptions

have been applied.

ym+1 =L

V

xm � B

V

xB

L VThe feed stage material balance relates L and V to and

y =

✓VB + 1

VB

◆x�

✓1

VB

◆xB

VB ⌘ V

Bboilup ratio

oper

atin

g lin

e

SHR §7.2.2

L = V +D

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Feed Stage & the “q-Line”

subcooled liquid saturated liquid partially vaporized saturated vapor superheated vapor

rectifying section

stripping section

liquid flow increase across feed rate normalized by feed rate.q =

L� L

F= 1 +

V � V

F

q > 1 q = 1 q = LF/F q = 0 q < 0

Operating lines & q-line must intersect at

a single point. ∴ cannot specify q, VB and R independently.

SHR §7.2.3

q =hsat. vaporF � hF

hsat. vaporF � hsat. liquid

F

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More on the q-line

y =L

V

x+D

V

xD

rectifying section:

y =L

V

x� B

V

xB

stripping section:

subtract

q =L� L

F= 1 +

V � V

F

y

✓V � V

F

◆=

✓L� L

F

◆x+ zF

y (1� q) = �qx+ zF

y =

✓q

q � 1

◆x� zF

q � 1

Typically the feed condition is known (specifying q).

Then we can choose VB or R.

Note: specifying R implies VB.

y

�V � V

�= x

�L� L

�+DxD +BxB| {z }

FzF

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Feed Stage & Number of Stagestoo low

too high

just right

Locate feed stage nearest to the intersection of the operating lines & q-line as possible (just after

the horizontal line on the staircase passes “P”

SHR §7.2.4

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Partial Reboilers & Condensers

F

D

B

V

L

L

VTotal Reboiler: • all liquid is turned back to vapor

Partial reboiler: • bottoms product is liquid, boilup is vapor

• This is another equilibrium stage! • very common...

Total condenser: • all vapor is condensed back to liquid

Partial condenser: • distillate is vapor, reflux is liquid

• This is another equilibrium stage!

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Limiting Cases: Rmin, Nmin.eq

uilib

rium

cur

ve

x

y

x = y

0 1.0

1.0

x = xDx = xB

equi

libriu

m c

urve

xy

x = y

0 1.0

1.0

x = zF

x = xDx = xB

“Total reflux” • R = ∞, VB = ∞. • L = V, D = B = F = 0. • F = 0, N = Nmin. • y = x is operating line. • No product...

“Minimum reflux” • N = ∞.

higher capital costshigher operating costs

x

y

x = y

0 1.0

1.0

x = xDx = xB

x = zF

1

2

3

“pinch point”

(L/V )min =Rmin

Rmin + 1

Rmin =(L/V )min

1� (L/V )min

(VB)min

=⇥�

L/V�max

� 1⇤�1

F

D

B

V

L

L

V

SHR §7.2.4

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Perfect Separation - Another “Limiting Case”

x

yx =

y

0 1.0

1.0

x = zF

Perfect separation: xB = 0, xD = 1. Pinch points form in each section of the column. Theoretical value for minimum reflux ratio and boilup to achieve perfect separation. To find this: • Obtain x-y data from thermo.

• Determine q-line

• Determine slope of rectifying operating line = Rmin/(Rmin+1).

Rmin =1

zF (↵� 1)For saturated liquid feed,

SHR §7.2.4

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ExampleWe want to separate a mixture of n-heptane and n-octane using distillation at

atmospheric pressure.

If the feed is 40 mole% n-heptane as a saturated vapor, determine the minimum reflux ratio and minimum number of stages required to obtain

product streams with 95% and 5% n-heptane.

F

D

B

V

L

L

V Known: • xD = 0.95 • xB = 0.05 • zF = 0.4, saturated vapor

Needed: • K-values (equilibrium curve) • q-line • operating lines

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