Oil Shale Pyrolysis Model

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Oil Shale Pyrolysis Modeling Ramesh Sarathi 28th Oil Shale Symposium Colorado School of Mines, Golden, CO October 13-17 2008

Transcript of Oil Shale Pyrolysis Model

Page 1: Oil Shale Pyrolysis Model

Oil Shale Pyrolysis Modeling

Ramesh Sarathi

28th Oil Shale SymposiumColorado School of Mines, Golden, CO

October 13-17 2008

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Overview

• Background– Pyrolysis process– Previous studies

• Model Description• Results• Conclusions

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Background

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Pyrolysis: (1) Heat Transfer

• Hot gases heat the surface of the particle

• Heat is conducted from the surface to the interior

r

Hot sweep gases

Surface heats first

qHeat is conducted to the interior

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Pyrolysis: (2) Chemical Reaction

• Temperature rise induces chemical reactions

• Endothermic reactions consume heat

• Rate of temperature rise slows

• Porosity is created as solid reactants form gaseous products

r

Hot sweep gases

Reactions start at surface

qReactions progress to interior

No sharp front

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Pyrolysis: (3) Mass & Momentum Transfer

• Momentum Transfer– Pressure buildup inside

particle causes gas to flow out

• Mass Transfer– Concentration gradients

cause products to diffuse out of particle

– Sweep gases diffuse into particle

– Thermal diffusion causes heavier molecules to diffuse toward cooler regions

r

Hot sweep gases

Low pressure, low species concentration at surface

Products flow out of particle

High pressure, high species concentration in interior

Civi

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Previous Studies• Experimental Studies

– Kerogen Pyrolysis• Campbell et al. [1978]

– Gas Evolution• Campbell et al. [1980] (2)• Huss & Burnham [1982]

– Oil Coking• Campbell et al. [1977]

– Oil Cracking• Bissell et al. [1983]

– Char Gasification• Burnham [1979] (3)• Thomson et al. [1983]

– Carbonate Minerals• Campbell [1978]

• Modeling Studies– Particle

• Johnson et al. [1975]• Campbell et al. [1977]• Shih & Sohn [1978]• Gregg et al. [1981]• Burnham & Braun [1985]• Wang & Lee [1986]

– Retort• Braun & Chin [1977/1981]• Tyner & Hommert [1978]• Crowl et al. [1979]• Parker & Zhang [2006]

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Model Description

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All models are wrong, some are useful.

~ George Box

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Objective

• Review previous studies

• Develop unified kinetic model

• Validate model with experimental data

Chemistry & Kinetics

Transport Phenomena(heat, mass)

Rock Mechanics

Phase Behavior

Production Rates & Yields

Heating Requirements

Process CostsLimiting Design Parameters

Model

Prediction

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Physical Model

r

Hot sweep gases

q

Civi

• Physical Model– Oil shale is heated in a furnace– Constant flow of inert gas

sweeps through reactor– Volatile products flow out of

reactor– Assume reactor is spatially

uniform• Chemistry

(adapted from LLNL studies)– Kerogen pyrolysis– Oil Coking, Cracking– Char pyrolysis– Char gasification, WGS– Carbonate decomposition

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Chemical Reactions

kerogen (5)

char

oil (11)

gas (2)

char’ char’’

CO2 CO

H2 H2O

dolomite

calcite

silicates

Pyrolysis

Carbonate Decomposition

Coking

Char Gasification

Cracking

Char Pyrolysis

gas

WGS

Solid GasKerogen (5) Oil vapor (11)

Char (3) CH4

Nahcolite CHx

Dawsonite H2

Dolomite H2O

Calcite CO

Silicates CO2

N2Char’ Pyrolysis

nahcolite

dawsonite

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KineticsReaction Kinetics Source

Kerogen Pyrolysis (5) 1st order Burnham & Braun [1985]Campbell et al. [1978]

Oil Coking (11) 1st order Burnham & Braun [1985]Campbell et al. [1977]

Oil Cracking (11) 1st order Burnham & Braun [1985]Bissell et al. [1983]

Char Pyrolysis (2) 1st orderGaussian-distributed Ea

Campbell et al. [1980]

Char Gasification (2) LHHW Burnham [1979] (3)*

Water-gas-shift 2nd order, reversible Braun & Chin [1981]

Carbonate Decomposition (7) 1st orderLHHW

Campbell [1978]

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Conservation Equations

VRfdt

dNj

jjis

is )1(,,, ε−⋅=∑

, , , , , , ,(1 )g i s i j s j g i j g jj j

N f R V f R Vε ε= ⋅ − + ⋅∑ ∑&

Solid Species Mole Balance

Gas Species Mole Balance

Accumulation Stoichiometry Reaction Volume ofRate Matrix Rate solid phase

⎧ ⎫ ⎧ ⎫ ⎧ ⎫ ⎧ ⎫=⎨ ⎬ ⎨ ⎬ ⎨ ⎬ ⎨ ⎬

⎩ ⎭ ⎩ ⎭ ⎩ ⎭ ⎩ ⎭

,, ,0 0 , ,

g ig i g i g i

dNC v C v N

dt= − + &

Accumulation Flow Flow Generation Rate In Out from reaction

⎧ ⎫ ⎧ ⎫ ⎧ ⎫ ⎧ ⎫= − +⎨ ⎬ ⎨ ⎬ ⎨ ⎬ ⎨ ⎬

⎩ ⎭ ⎩ ⎭ ⎩ ⎭ ⎩ ⎭

,0 ,T T g ii

F F N= +∑ &

0,0 0

T

T

F Tv vF T

⎛ ⎞⎛ ⎞= ⎜ ⎟⎜ ⎟⎜ ⎟⎝ ⎠⎝ ⎠

Inlet Molar Outlet Molar Generation Flowrate Flowrate from Reaction⎧ ⎫ ⎧ ⎫ ⎧ ⎫

= +⎨ ⎬ ⎨ ⎬ ⎨ ⎬⎩ ⎭ ⎩ ⎭ ⎩ ⎭

Inlet Volumetric Outlet Volumetric Ratio of Flowrate Flowrate Molar Flowrates⎧ ⎫ ⎧ ⎫⎧ ⎫

=⎨ ⎬ ⎨ ⎬⎨ ⎬⎩ ⎭ ⎩ ⎭⎩ ⎭

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Solution Method

• 0D Model– Each mole balance equation is an ODE– Furnace temperature increases linearly with

time– Retort sweep gas flow rate determines

product residence time– Integrate ODE system with MATLAB

ODE15s

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Results

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Oil Production

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Methane Production

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H2 Production

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CO2 Production

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Conclusions

• Kinetic model can reproduce trends in laboratory data

• Next Steps– Improve lumped species model for oil

composition– Perform sensitivity analyses– Develop particle model w/ mass and heat

transport

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Questions?

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Conservation Equations: 1D

( )_

, ,·n rxn

s p s s rxn j jj

Tc T h Rt

ρ λ∂= ∇ ∇ −

∂ ∑

( ), ,, , ,

,

·g i g ii m g i g i

g t

C CD p C R

t Cφ κ

μ−

+∂ ⎛ ⎞

= ∇ ∇ ∇ +⎜ ⎟⎜ ⎟∂ ⎝ ⎠&

( ),,

(1 ) s is i

CR

tφ∂ −

=∂

&

Solid-phase Mass Balance

Gas-phase Mass Balance

Particle Energy Balance

{ } { }Solid Accumulation Reaction=

{ } { } { } { }Gas Accumulation Diffusion Convection Reaction= + +

{ } { } { }Heat Acummulation Conduction Generation by Reaction= +