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Supercritical Fluid Chromatography SFC Chromatographic Fundamentals Practical Verification of SFC Theoretical Description of SFC / Scale-up SFC on a Preparative.

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Presentation on theme: "Supercritical Fluid Chromatography SFC Chromatographic Fundamentals Practical Verification of SFC Theoretical Description of SFC / Scale-up SFC on a Preparative."— Presentation transcript:

1 Supercritical Fluid Chromatography SFC Chromatographic Fundamentals Practical Verification of SFC Theoretical Description of SFC / Scale-up SFC on a Preparative Scale: Examples Prostaglandins, Tocopherols DHA / DPA, Phytol On-line Analysis with SFC Continuous Chromatography: SMB Chapter 8 Chromatography with Supercritical Fluids

2 . Mode of Operation: Elution chromatography

3 Elution Chromatography: A Chromatogram

4 Mass transport high Solvent power high Schoenmakers, Uunk 1987 Different Mobile Phases

5 SFC: Stationary Phases

6 SFC: Different Gases as Mobile Phase

7 SFC: Different Modifiers

8 SFC: Influence of Pressure and Temperature

9 SFC: Pressure And Density Programming

10 Overloading by volume Analytical injection Overloading by concentration Concentration Time Chromatograms For Different Amounts of Injection

11 Adsorption Isotherms And Corresponding Chromatograms

12 SFC: Flow Scheme of Apparatus

13 Elution Chromatography: A Chromatogram

14 Capacity Ratio

15 Capacity Factors

16 with n = number of stages for p: Chromatographic Separation

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20 Selectivity Resolution Chromatographic Separation

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22 Van Deemter Chromatographic Separation

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24 SFC Analytical Scale, hp

25 Influence of temperature Preparative separation Chromatograms of fractions Upnmoor 1992 Separation of Prostaglandins

26 Separation of Tocopherols

27 Influence of modifier concentration Separation of Tocopherols

28 82 84 86 88 90 92 94 96 98 01234567 250 x 4.6 pS 250 x 8.0 pS specific productivity DHA [mg/cm 3 h] Area DHA GC [%] 1mg DHA/(h,cm 3 ) * 500 ml = 0,5 g DHA/h Some kg DHA:Fully automatized plant ! RF=0,842 Productivity: DHA / DPA Separation by SFC

29 Dynamic axial compressed SFC column; Dimensions: ID = 30 mm, length of packing: 0 to 190 (type I), 0 to 450 mm (type II) P max 400 bar, T max 200 °C. SMB- Plant: Separation Columns

30 SFC, Preparative Scale

31 Rotating columnRotating ports Continuous Chromatography

32 Extract A + D Raffinate B + D Feed A + B + D Desorbent D Zone 1 Purification of Adsorbent Zone 3 Enrichment of B Zone 4 Purification of Desorbent Zone 2 Enrichment of A True Moving Bed (TMB) Process

33 Principle of Simulated Countercurrent Separation Mazzotti, ETH-Z

34 Extract A+D Raffinate B+D Feed A+B Desorbens D Concentration A, B Simulated Moving Bed-Process

35 Gottschall: PREP 95 Performance SMB vs Elution (99.5 % Purity)

36 Preparative SMB-Plant Depta, 2000

37 Adsorption isotherms for Phytol cis- and trans- isomer (black lines) and derivatives (red lines). 225 bar, 40 °C, 1.8 mass% isopropanol as modifier. Isotherms exhibit a point of inflection for each isomer. Adsorption Isotherms

38 Experimental and simulated phytol chromatogramssymbols: experimental data; lines: simulations. Batch-Simulations

39 Model: equilibrium, axially dispersed plug flow with variable velocity of mobile phase, Pressure drop: Ergun equation, Properties of mobile phase (CO 2 ) calculated with equation of state. SMB process modeled with four key parameters: the net flow ratios m j: Ruthven, Storti. SMB-Simulation

40 SMB- SFC: Volume-flow is a function of column length. Therefore, net flow ratios are not constant in each zone. New parameter: Representation of SMB-SFC process in a (m 2 * -m 3 * )-plane, solution of mass balance equations with finite difference method [Kniep et al.], adapted to variable velocity of mobile phase. The algorithm is fast enough to calculate the region of complete separation in the (m 2 * -m 3 * )-plane numerically, taking into account: any type of isotherm equation axial dispersion number of used columns change in mobile phase density SMB-Simulation

41 operating point black triangles:infinite dilution situation and infinite number of theoretical plates same parameter set as operating point in figure 5 Region of complete separation for phytol C feed =5.0 mg/ml 230 bar, no pressure drop, columns: 2/2/2/2; 300 plates per column Columns: 1/1/1/1; 1000 plates per column SMB-Simulation: Phytol Separation

42 operating point black triangles:infinite dilution situation and infinite number of theoretical plates same parameter set as operating point in figure 5 Region of complete separation for phytol C feed =5.0 mg/ml 230 bar, no pressure drop, columns: 2/2/2/2; 300 plates per column Columns: 1/1/1/1; 1000 plates per column SMB-Simulation: Phytol Separation

43 Region of complete separation for phytol, infinite dilution, columns: 2/2/2/2; 300 plates per column, 230 bar, no pressure drop Same as in left figure but calculations with pressure drop Pressure drop leads to a shift of the complete separation region to lower values of m 2 * and m 3 * SMB-Simulation: Phytol Separation

44 low concentration in Feed linear Adsorption isotherm Ideal model 1 2 3 Experimental Results of Ibuprofen Separation

45 140 mg Racemate /min; 2/2/3/1 configuration Separation of Ibuprofen

46 Verunreinigungen Phytolisomere Conditions of separation: 240 bar, 50°C, column 4 x 250 mm packed with LiChrospher 100 (Silica), flow 2,56 g carbon dioxide / min, modifier 3wt.-%EtOH, productivity 45 mg/(ml, h). 17mg pur 0,85 mg in Hexan OH CH 3 CH 3 CH 3 CH 3 HH CH 3 Phytol Diterpene-alcohol, Intermediate for vitamin E, K1 esterified lipophiliccompound of chlorophyll


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