Supplementary material (S1) - Springer Static Content Server

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NH3-SCR activity of H-BEA and Fe-BEA
after potassium exposure
Soran Shwan
a,*
b
a
a
, Jonas Jansson , Louise Olsson and Magnus Skoglundh
a
Competence Centre for Catalysis, Chalmers University of Technology, SE-412 96
Gothenburg, Sweden
b
Volvo Group Trucks Technology, SE-40508, Gothenburg, Sweden
*
Corresponding author:
Soran Shwan
Competence Centre for Catalysis and
Department of Applied Surface Chemistry
Chalmers University of Technology
SE-41296 Göteborg, Sweden
Telephone: +46 (0)31 772 2943
Email: soran@chalmers.se
Supplementary material (S1)
Nomenclature list
𝐴𝑖
π‘π‘˜
π‘π‘˜π΅
π‘‘β„Žπ‘¦π‘‘
π·π‘˜,𝑔
πΈπ‘Ž,𝑖
𝐺𝑆𝐴
βˆ†π»
π‘˜π‘˜,π‘š
𝐾
π‘˜π‘–
π‘€πΊπ‘˜,𝑔
π‘Ÿπ‘–
𝑅
βˆ†π‘†
Sh
π‘Š
π‘π΅π‘Ÿ,1
π‘π΅π‘Ÿ,2
𝐹𝑒𝑀,1
𝐹𝑒𝑀,2
𝐹𝑒𝐷
𝐹𝑒𝑃
𝑇𝑠
𝑑
π‘£π‘˜,𝑖
𝑣𝑔
π‘€π‘˜,𝑔
𝑧
Pre-exponential factor for reaction i. Depends on the rate expression
Mole fraction at the reaction layer of species k (-)
Mole fraction in the gas bulk of species k (-)
Hydraulic diameter of the channel (m)
Diffusion coefficient of species k in the gas bulk
Activation energy for reaction i (J/mol)
Geometric surface area per reactor volume (m-1)
Enthalpy change (kJ/mol)
Mass transfer coefficient of species k (mol/ m2 s)
Equilibrium constant (-)
Rate constant for reaction i. Depends on the rate expression
Molar mass of gas phase species k (kg/kmol)
Reaction rate for reaction i (kmol/s m3wash-coat)
Gas constant (J/mol K)
Entropy change (J/mol K)
Sherwood number (-)
Weak zeolite adsorption site
Brønsted zeolite site, 1
Brønsted zeolite site, 2
Monomeric iron site, 1
Monomeric iron site, 2
Dimeric iron site
Iron particle site
Temperature at catalyst surface (K)
Time (s)
Stoichiometric coefficient of species k in reaction i
Gas velocity (m/s)
Mass fraction of species k in gas phase (-)
Spatial coordinate in axial direction (m)
Greek letters
π›Όπ‘˜,𝑖
πœ€π‘”
πœƒπ‘˜
πœŒπ‘”
Θ𝑗
Coverage dependence for species k in reaction i (-)
Volume fraction of gas phase in entire system (-)
Coverage of species k (-)
Density of the gas phase (kmol/ m3)
Surface site density of storage site j (mol/ m2)
The kinetic model
The main governing equation for the gas phase species for a single channel model is [1]:
εg
∂ρg βˆ™ wk,g
∂t
= εg
∂ρg βˆ™ wk,g βˆ™ vg
∂z
+ MGk,g ∑nr
i vi,k βˆ™ ri (ck , Ts , θk )
(Eq.1)
The coverage of component k on the surface is solved by [1]:
∂θk
(Θ
∂t
βˆ™ GSA) = ∑nr
i vi,k βˆ™ ri (ck , Ts , θk )
(Eq.2)
The geometric surface area per unit reactor volume, GSA, in Eq. (2) is given by [1]:
GSA
dhyd
= 4 × (cell density)
(Eq.3)
Furthermore, mass-transport from gas bulk to the catalytic surface and vice versa is included. Under
quasi steady-state conditions, the rates of the surface reactions balance the diffusive transport from the
gas bulk to the surface. The molar surface concentration (ck) of component k is evaluated using [1],
GSA βˆ™ k k,m βˆ™ (ck − ckB ) = ∑nr
i vi,k βˆ™ ri (ck , Ts , θk )
(Eq.4)
where ckB is the concentration of species k in the gas bulk and k k,m is the mass transfer coefficient of
the individual species calculated according to [1]:
k k,m =
Shβˆ™ Dk,g
dhyd
(Eq. 5)
where Dk,g is the diffusion coefficient of species k in the gas mixture and the Sherwood number is
calculated according to the Sieder/Tate relationship [2].
Supplementary material (S2)
Figure S1. Schematic summary of the active sites and their corresponding reactions in the kinetic
deactivation model for Fe-BEA.
Table 1:Reactions and rate expressions for NH3 and NO adsorption and desorption (W represents
sites for weakly bound ammonia. ZBr and FeM represent Brønsted and monomeric iron sites,
respectively)
Reaction number
Reaction
Reaction rate
1
𝑁𝐻3 + π‘Š ⇔ 𝑁𝐻3 − π‘Š
π‘Ÿ1 = π‘˜1,𝑓 𝑐𝑁𝐻3 πœƒπ‘Š−π‘£π‘Žπ‘π‘Žπ‘›π‘‘ − π‘˜1,𝑏 πœƒπ‘π»3−π‘Š
2
𝑁𝐻3 + π‘π΅π‘Ÿ,1 ⇔ 𝑁𝐻3 − π‘π΅π‘Ÿ,1
π‘Ÿ2 = π‘˜2,𝑓 𝑐𝑁𝐻3 πœƒπ‘π΅π‘Ÿ,1−π‘£π‘Žπ‘π‘Žπ‘›π‘‘ − π‘˜2,𝑏 πœƒπ‘π»3−π‘π΅π‘Ÿ,1
3
𝑁𝐻3 + π‘π΅π‘Ÿ,2 ⇔ 𝑁𝐻3 − π‘π΅π‘Ÿ,2
π‘Ÿ3 = π‘˜3,𝑓 𝑐𝑁𝐻3 πœƒπ‘π΅π‘Ÿ,2−π‘£π‘Žπ‘π‘Žπ‘›π‘‘ − π‘˜3,𝑏 πœƒπ‘π»3−π‘π΅π‘Ÿ,2
4
𝑁𝐻3 + 𝐹𝑒𝑀,1 ⇔ 𝑁𝐻3 − 𝐹𝑒𝑀,1
π‘Ÿ4 = π‘˜4,𝑓 𝑐𝑁𝐻3 πœƒπΉπ‘’π‘€,1−π‘£π‘Žπ‘π‘Žπ‘›π‘‘ − π‘˜4,𝑏 πœƒπ‘π»3−𝐹𝑒𝑀,1
5
𝑁𝐻3 + 𝐹𝑒𝑀,2 ⇔ 𝑁𝐻3 − 𝐹𝑒𝑀,2
π‘Ÿ5 = π‘˜5,𝑓 𝑐𝑁𝐻3 πœƒπΉπ‘’π‘€,2−π‘£π‘Žπ‘π‘Žπ‘›π‘‘ − π‘˜5,𝑏 πœƒπ‘π»3−𝐹𝑒𝑀,2
𝑁𝐻3 − π‘π΅π‘Ÿ,1 + 𝐹𝑒𝑀,1 ⇔ π‘π΅π‘Ÿ,1 + 𝑁𝐻3 − 𝐹𝑒𝑀,1
π‘Ÿ6 = π‘˜6,𝑓 πœƒπ‘π»3−π‘π΅π‘Ÿ,1 πœƒπΉπ‘’π‘€,1−π‘£π‘Žπ‘π‘Žπ‘›π‘‘ − π‘˜6,𝑏 πœƒπ‘π΅π‘Ÿ,1−π‘£π‘Žπ‘π‘Žπ‘›π‘‘ πœƒπ‘π»3−𝐹𝑒𝑀,1
7
𝑁𝑂 + π‘π΅π‘Ÿ,2 ⇔ 𝑁𝑂 − π‘π΅π‘Ÿ,2
π‘Ÿ7 = π‘˜7,𝑓 𝑐𝑁𝑂 πœƒπ‘π΅π‘Ÿ,2−π‘£π‘Žπ‘π‘Žπ‘›π‘‘ − π‘˜7,𝑏 πœƒπ‘π‘‚−π‘π΅π‘Ÿ,2
8
𝑁𝑂 + 𝐹𝑒𝑀,2 ⇔ 𝑁𝑂 − 𝐹𝑒𝑀,2
π‘Ÿ8 = π‘˜8,𝑓 𝑐𝑁𝑂 πœƒπΉπ‘’π‘€,2−π‘£π‘Žπ‘π‘Žπ‘›π‘‘ − π‘˜8,𝑏 πœƒπ‘π‘‚−𝐹𝑒𝑀,2
6a,b
a
b
– Thermodynamically restricted (cf. 3.2.1).
– Reaction rate is independent of the corresponding site densities.
Table 2:Reactions and rate expressions for NH3 and NO oxidation.
Reaction number
9a
10b
11c,e
12d,e
Reaction
Reaction rate
4𝑁𝐻3 + 3𝑂2 ⇒ 2𝑁2 + 6𝐻2 𝑂
π‘Ÿ9 = π‘˜9 𝑐𝑁𝐻3 𝑐𝑂2
4𝑁𝐻3 + 3𝑂2 ⇒ 2𝑁2 + 6𝐻2 𝑂
π‘Ÿ10 = π‘˜10 𝑐𝑁𝐻3 𝑐𝑂2
2𝑁𝑂 + 𝑂2 ⇔ 2𝑁𝑂2
2𝑁𝑂 + 𝑂2 ⇔ 2𝑁𝑂2
proceeds over site π‘π΅π‘Ÿ,2 (Θπ‘π΅π‘Ÿ,2 ).
π‘Ÿ11 = π‘˜11,𝑓 𝑐𝑁𝑂 𝑐𝑂0.5
− π‘˜11,𝑏 𝑐𝑁𝑂2
2
π‘Ÿ12 = π‘˜12,𝑓 𝑐𝑁𝑂 𝑐𝑂0.5
− π‘˜12,𝑏 𝑐𝑁𝑂2
2
– Reaction rate (r9)
– Reaction rate (r10) proceeds over site 𝐹𝑒𝐷 (Θ𝐹𝑒𝐷 )
c
– Reaction rate (r11) proceeds over site π‘π΅π‘Ÿ,2 (Θπ‘π΅π‘Ÿ,2 ).
d
– Reaction rate (r12) proceeds over site 𝐹𝑒𝑃 (Θ𝐹𝑒𝑃 ).
e
– π‘˜11,𝑏 and π‘˜12,𝑏 are calculated from the thermodynamic restrictions (βˆ†π» = 58.3 kJ/mol and
βˆ†π‘† = -76.1 J/mol K) [3]
a
b
Table 3:Reactions and rate expressions for NH3-SCR (ZBr and FeM represents Brønsted and
monomeric iron sites, respectively).
Reaction number
Reaction
Reaction rate
13
4𝑁𝐻3 − π‘π΅π‘Ÿ,1 + 4𝑁𝑂 − π‘π΅π‘Ÿ,2 +𝑂2 ⇒ 4𝑁2 + 6𝐻2 𝑂 + 4π‘π΅π‘Ÿ,1 + 4π‘π΅π‘Ÿ,2
π‘Ÿ13 = π‘˜13 𝑐𝑂2 πœƒπ‘π»3−π‘π΅π‘Ÿ,1 πœƒπ‘π‘‚−π‘π΅π‘Ÿ,2
14
4𝑁𝐻3 − 𝐹𝑒𝑀,1 + 4𝑁𝑂 − 𝐹𝑒𝑀,2 +𝑂2 ⇒ 4𝑁2 + 6𝐻2 𝑂 + 4𝐹𝑒𝑀,1 + 4𝐹𝑒𝑀,2
π‘Ÿ14 = π‘˜14 𝑐𝑂2 πœƒπ‘π»3−𝐹𝑒𝑀,1 πœƒπ‘π‘‚−𝐹𝑒𝑀,2
4𝑁𝐻3 + 4𝑁𝑂 +𝑂2 ⇒ 4𝑁2 + 6𝐻2 𝑂
π‘Ÿ15 = π‘˜15 𝑐𝑂2 𝑐𝑁𝐻3 𝑐𝑁𝑂
15a
a
– Reaction rate (r15) proceeds over the dimeric iron sites (Θ𝐹𝑒𝐷 ).
Table 4:Kinetic parameters for NH3 and NO adsorption and desorption reactions.
Rate
NH3 adsorption (π‘Ÿ1,𝑓 )
NH3 desorption (π‘Ÿ1,𝑏 )
Rate constants
π‘˜1,𝑓 a
π‘˜1,𝑏 a
Pre-exponential factor
1.76x102
2.44 x104
Activation energy (kJ/mol)
0
53.23
Coverage dependence(𝛼)
0
0.98
NH3 adsorption (π‘Ÿ2,𝑓 )
NH3 desorption (π‘Ÿ2,𝑏 )
π‘˜2,𝑓 a
π‘˜2,𝑏 a
2.05x102
2.97 x105
0
79.59
0
0.066
NH3 adsorption (π‘Ÿ3,𝑓 )
NH3 desorption (π‘Ÿ3,𝑏 )
π‘˜3,𝑓 a
π‘˜3,𝑏 a
3.4882x104
5.05 x107
0
79.59
0
0.066
NH3 adsorption (π‘Ÿ4,𝑓 )
NH3 desorption (π‘Ÿ4,𝑏 )
π‘˜4,𝑓 a
π‘˜4,𝑏 a
3.29x102
5.01x102
0
72.98
0
0.07
NH3 adsorption (π‘Ÿ5,𝑓 )
NH3 desorption (π‘Ÿ5,𝑏 )
π‘˜5,𝑓 a
π‘˜5,𝑏 a
3.23x103
2.07 x106
0
72.98
0.07
NH3 spillover (π‘Ÿ6,𝑓 )
π‘˜6,𝑓 b
2.18x103
65.75
0
NO adsorption (π‘Ÿ7,𝑓 )
NO desorption (π‘Ÿ7,𝑏 )
π‘˜7,𝑓 a
π‘˜7,𝑏 a
7.94x103
6.32 x105
0
105.81
0
NO adsorption (π‘Ÿ8,𝑓 )
NO desorption (π‘Ÿ8,𝑏 )
π‘˜8,𝑓 a
π‘˜8,𝑏 a
2.78x103
7.6 x105
0
65.29
0
a
b
– Unit: 1/(s m)
– Unit: m/(kmol s)
Table 5:Kinetic parameters for NH3 and NO oxidation reactions.
Rate
NH3 oxidation (π‘Ÿ9 )
NH3 oxidation (π‘Ÿ10 )
Rate constants
π‘˜9 a
π‘˜10 a
NO oxidation (π‘Ÿ11,𝑓 )
NO oxidation (π‘Ÿ12,𝑓 )
a
Pre-exponential factor
8.76x106
9.22 x1014
Activation energy (kJ/mol)
83.14
166.14
8.32x103
8.07 x104
π‘˜11,𝑓 a
π‘˜12,𝑓 a
8.71
20.03
– Unit: 1/(s m)
Table 6:Kinetic parameters for the NH3 SCR reactions.
Rate
Standard SCR, zeolite (π‘Ÿ13 )
Standard SCR, monomeric (π‘Ÿ14 )
Standard SCR, dimeric (π‘Ÿ15 )
a
b
– Unit: m/(kmol s)
– Unit: 1/(s m)
Rate constants
π‘˜13 a
π‘˜14 a
π‘˜15 b
Pre-exponential factor
4.16x109
2.89x108
2.65 x1015
Activation energy (kJ/mol)
85.7
36.2c
93c
c
– Parameter fixed from Brandenberger et al. [4]
References
[1]AVL BOOST Aftertreatment manual, AVL, www.avl.com, 2011.
[2]J.R. Welty, C.E. Wicks, R.E. Wilson, G. Rorrer, Fundamentals of Momentum, Heat, and Mass
Transfer, John Wiley & Sons, Inc, USA, 2001.
[3]A. Lindholm, N.W. Currier, J.H. Li, A. Yezerets, L. Olsson, J. Catal. 258 (2008) 273-288.
[4]S. Brandenberger, O. Kröcher, A. Tissler, R. Althoff, Applied Catalysis B: Environmental 95
(2010) 348-357.
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