Optimisation and control of chromatography - PowerPoint PPT Presentation

About This Presentation
Title:

Optimisation and control of chromatography

Description:

Laboratory of Process Control. Biochemical and Chemical Engineering Department ... Considerable amount of pure chiral drugs. is required for the clinical phases. ... – PowerPoint PPT presentation

Number of Views:215
Avg rating:3.0/5.0
Slides: 31
Provided by: toumie
Category:

less

Transcript and Presenter's Notes

Title: Optimisation and control of chromatography


1
Optimisation and control of chromatography
Sebastian Engell Abdelaziz Toumi Laboratory of
Process ControlBiochemical and Chemical
Engineering Department Universität Dortmund
2
Contents
  • Introduction
  • Preparative chromatography
  • Simulated Moving Bed technology
  • Reactive chromatography
  • Batch chromatography
  • Motivation, problem formulation, modelling
  • Parameter estimation
  • Feedback control
  • SMB chromatography
  • Optimisation of the operation regime
  • Control strategies
  • Optimisation-based control of a reactive
    SMB-process
  • Conclusions and future challenges

3
Preparative chromatography
Preparative chromatography Chromatography for
production, not analytical chemistry Batch
Process
  • flexible, standard process in analytical and
    development labs
  • multi-components separation
  • intensification by gradient elution
  • expensive in large scale
  • highly diluted products

4
Simulated Moving Bed technology
Process intensification True Moving Bed (TMB)
  • Practical implementation as a
  • simulated moving bed process
  • Adsorbent is fixed in several chromatographic
    columns.
  • Periodic switching of the inlet/outlets gt
    moving bed is simulated.
  • Complex mixed discrete and continuous dynamics

5
SMB chromatography process dynamics
  • Continuous flows and discrete switchings
  • Axial profile builds up during start-up
  • Same profile in different columns in cyclic
    steady state
  • Periodic output concentrations

6
The VARICOL process
  • Variable length column process (NovaSEP 2000)
  • Periodic but asynchronous switching of the
    ports

7
Industrial applications of SMB I
  • Petro-chemicals
  • Universal Oil Products (USA), US Patent
    (Brougthon und Gerhold 1961), 120 units sold
    (Sarex?, Molex ?, Parex? etc..)
  • Institut Francais du Pétrole (France), largest
    SMB-Plant in the world implemented in South Korea
    (Eluxyl?)
  • .
  • Sugar industry
  • Amalgamated Sugar Co. (USA) operates SMB-plants
    with a total capacity of 24.500 tonn HFCS (2001)
  • Cultor Corporation (Finland) patented new
    operating modes which includes ,,Sequential-
    and ,,Multistage SMB (FAST?)
  • Appelxion has installed more than 90 ,,Improved
    SMB-Plants, 3 of them in Europe (in Spain for the
    production of Pinitol)
  • .

8
Industrial applications of SMB II
  • Pharmaceutical substance development
  • Considerable amount of pure chiral drugs is
    required for the clinical phases.
  • Binary separations of enantiomers
  • Drugs purified using SMB-processes
  • Prozac? (Elli Lilly Co, USA)
  • Citalopram? (Lundbeck, Denmark)
  • ...
  • SMB-Plants of large scale
  • Aerojet Fine Chemicals (Sacramento, USA)
  • Bayer (Leverkusen, Germany)
  • Daicel (Japan)
  • Novasep (Nancy, France)
  • ...

800 Millimeters SMB-Plant Aerojet Fine Chemicals
(Sacramento, USA)
9
Prediction of application areas
Fraction of installed units
10
Reactive chromatography
  • Integration reduces equipment costs.
  • In-situ adsorption drives the reaction beyond the
    equilibrium.
  • Conversion of badly separable components
  • Loss of degrees of freedom and flexibility
  • Complex dynamics, narrow range of operation

A
BC
Injection
A
B
A
C
Chromatographic bed catalyst
  • Mazzotti/Morbidelli et al. (ETH-Zürich)
  • Ray et al. (Singapore National University)
  • Schmidt-Traub et al. (Universität Dortmund)
  • DFG-Research Cluster Integrated Reaction and
    Separation Processes at Universität Dortmund
    since 1999

fractionation
tanks
A
B
C
11
RSMB for glucose isomerisation (Fricke and
Schmidt-Traub)
  • 6 columns interconnected in a closed loop
    arrangement
  • ion exchange resin (Amberlite CR-13Na)
  • immobilized enzyme Sweetzyme T (Novo Nordisk
    Bioindustrial)

12
Contents
  • Introduction
  • Preparative chromatography
  • Simulated Moving Bed technology
  • Reactive chromatography
  • Batch chromatography
  • Motivation, problem formulation, modelling
  • Parameter estimation
  • Feedback control
  • SMB chromatography
  • Optimisation of the operation regime
  • Control strategies
  • Optimisation-based control of a reactive
    SMB-process
  • Conclusions and future challenges

13
Batch chromatography challenge
  • Separation of 2-component mixtures in isocratic
    elution mode
  • Goals
  • Maximize productivity for given column setup!
  • Meet product specifications at all times!
  • Adjust for
  • plant/model mismatch or
  • changes in separation characteristics!
  • Extension of this concept to multi-component
    mixtures

14
Batch chromatography optimisation
  • Mathematical formulation of the optimisation
    problem
  • maximise the productivity
  • purity requirements
  • recovery requirements
  • flow rate limitationdue to maximum pressure drop

Online optimisation nested approach (Dünnebier
Klatt)
15
General Rate Model
Numerical Scheme by Gu
Solid phase
Parabolic pde system
Fluid phase
  • Simulation is 2-5 orders of magnitude faster than
    real time.
  • Universal model, can include reaction etc..

16
Batch chromatography Parameter estimation -
results
  • Enantiomer separation
  • EMD 53986 by MERCK, Darmstadt
  • R fast eluting
  • Initial set of model parameters from offline
    experiments
  • Model adaptation by online estimation of
  • 1 mass transfer coefficient
  • 1 adsorption parameter per component
  • good fit of measured and simulated elution
    profiles

17
Batch chromatography Control scheme
18
Batch chromatographyControl results for sugar
separation
  • Task
  • Reach steady state after initial disturbance!
  • Realise set-point change!
  • Specifications of the experiment
  • System Fructose (A) Glucose (B)
  • Feed concentration 30 mg/ml each
  • Specified purities 80 each New
    Setpoints 85 each

19
Dealing with model mismatch
  • Unfeasible set-point
  • Constraints are violated.
  • The process is operated inefficiently.

Model mismatch
  • Additional feedback control layer to establish
    the constraints

20
Feedback control
Hanisch 2002
Adjust switching times to keep the purity
constraints
Adjust operating parameters to minimize the waste
part
21
Online optimisation
Disadvantage of the purity control
scheme Optimality is lost! Solution
Measurement-based online optimisation
  • Redesigned ISOPE algorithm
  • Combines the measurement information and the
    model to construct a modified optimisation
    problem.
  • Iteratively converging to the real optimum
    although model mismatch exists.
  • Can handle constraints with model mismatch.

Gao Engell Measurement-based online
optimisation with model-mismatch, ESCAPE 14.
22
Simulation study enantiomer separation
Elution profiles
Purity specification 98 Recovery limit
80 Flow rate 0.42 cm/s
real plant
Production rate surfaces
Real plant
Optimisation model
23
Result of iterative optimisation
24
Contents
  • Introduction
  • Preparative chromatography
  • Simulated Moving Bed technology
  • Industrial applications of SMB
  • Reactive chromatography
  • Batch chromatography
  • Motivation, problem formulation, modelling
  • Parameter estimation
  • Feedback control
  • SMB chromatography
  • Optimisation of the operation regime
  • Control strategies
  • Optimisation-based control of a reactive
    SMB-process
  • Conclusions and future challenges

25
Reminder SMB dynamics
26
Choice of the (nominal) operating regime
  • Triangle theory (Morbidelli and Mazzotti)
  • Based on the True Moving Bed process model
  • Wave theory (Ma Wang 1997)
  • HELPCHROM (Novasep)
  • Based on a plate model, propriatory software
  • Approaches based on rigorous modelling
  • Heuristics, simulation-based-methods
    (Schmidt-Traub et al., Biressi et al.)
  • Genetic algorithms (Zhang et al. 2003)
  • Iterative approach (Lim and Joergensen, 2004)
  • SQP-based approach (Klatt and Dünnebier, Toumi)

27
Mathematical modeling Full model
  • Hybrid Dynamics
  • Node Model (change in flow rates and
    concentration inputs)
  • Synchronuous switching (new initialization of the
    state)
  • Continuous chromatographic model (General Rate
    Model)
  • Numerical approach (Gu, 1995, Toumi)
  • Finite Element Discretization of the fluid phase
  • Orthogonal Collocation for the solid phase
  • stiff ordinary differential equations solved by
    lsodi (Hindmarsh et al.)
  • Efficient and accurate process model (672 state
    variables for nelemb10, nc1,Ncol8)

28
Model-based Optimisation I
  • Sequential approach
  • simulation until cyclic steady state is reached
  • Simultaneous/multiple shooting
  • cyclic steady state is included as an additional
    constraint

Process dynamic cyclic steady state
Purities
Pressure drop
SMBOpt (Toumi et. al.)
29
SMB vs. VARICOL (single shooting)
Verzögerer
  • VARICOL is more efficient than SMB
  • VARICOL result gives clue for the choice of
    the distribution of the columns over the zones.

30
SMB vs. PowerFeed (multiple shooting)
SMB
PowerFeed
  • 26.0 higher Productivity
Write a Comment
User Comments (0)
About PowerShow.com