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Veröffentlicht von:Walburga Kesler Geändert vor über 11 Jahren
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Neue Produkte auf der Basis von Glycerin
Prof. Dr. Arno Behr Universität Dortmund Nachwachsende Rohstoffe für die Chemie Oldenburg, 28. –
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Triglyceride + 3 Methanol → 3 Methylester + Glycerol “Biodiesel“
by-product in oleochemistry Triglyceride + 3 Methanol → 3 Methylester + Glycerol “Biodiesel“ 1 t biodiesel ~ 110 kg crude glycerol Production of biodiesel in Europe: estimated for 2010: 7 – 8 Mill. t/a Prize of glycerol: decreasing from → 500 €/t
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Chemical functionalization
Present applications of glycerol Glycerol Direct applications Chemical functionalization pharmaceuticals cosmetics soaps sweetener moistening of tobacco triesters glycerol trinitrate polyether glycols alkyd resins
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Contents Glycerol Alkyl ethers Alkenyl ethers (telomers) Oligomers Polymers Oxidation products Carbonylation products Other derivatives
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Glycerol-tertiary-butyl-ethers (GTBE)
R1, R2, R3 = H, But + n [H+] Acid catalyst Glycerol Isobutene GTBE Monoethers (m-GTBE) n = 1 1-GTBE 2-GTBE Higher ethers (h-GTBE) diesel-additive n = 2, 3 1,3-GTBE 1,2-GTBE 1,2,3-GTBE
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Measurement of kinetics
catalyst: p-toluene- sulfonic acid T = 90°C Isobutene : glycerol = 2:1 phase behavior
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Reactor Extraction Flash Rectification
Process diagram Reactor °C 20-30 bar Extraction 30-40 °C 20-30 bar Flash 30-40 °C 1 bar Rectification 75 °C 5 mbar Isobutene recirculation h-GTBE Glycerol Isobutene R1 R2 R1 = recirculation of glycerol, pTS, m-GTBE R2 = recirculation of m-GTBE pTS = p-toluenesulphonic acid
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Contents Glycerol Alkyl ethers Alkenyl ethers (telomers) Oligomers Polymers Oxidation products Carbonylation products Other derivatives
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Potential applications: detergent precursors
Glycerol alkenyl ethers (Telomers) Potential applications: detergent precursors
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Triphenylphosphinsulfonate (TPPTS)
Plant concept for the production of glycerol telomers catalyst: Pd/ TPPTS Triphenylphosphinsulfonate (TPPTS)
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Contents Glycerol Alkyl ethers Alkenyl ethers (telomers) Oligomers Polymers Oxidation products Carbonylation products Other derivatives
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Glycerol oligomers The reaction can be carried out both acid and base catalyzed The acid catalyzed reaction leads to unwanted by-products Applications: foods, cosmetics, pharmacy, educt for glycerol esters
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Plant concept for the production of glycerol oligomers
Reactive distillation: Simultaneous reaction and separation within one apparatus On account of continuous withdrawing of the by-product water the glycerol conversion is increased A higher selectivity can be achieved because of a defined contact time of the glycerol with the heterogeneous catalyst But: Difficult to engineer on account of complex relationships between process parameters catalyst: molecular sieves
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Contents Glycerol Alkyl ethers Alkenyl ethers (telomers) Oligomers Polymers Oxidation products Carbonylation products Other derivatives
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Hyperbranched polyglycerols
Glycerol polymers Hyperbranched polyglycerols
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Contents Glycerol Alkyl ethers Alkenyl ethers (telomers) Oligomers Polymers Oxidation products Carbonylation products Other derivatives
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Glycerinoxidation Pt-Bi/C Pd/C Pt/C Au/C Sauerstoff Kohlenstoff
Dihydroxyaceton Hydroxybrenztraubensäure Glyceraldehyd Glycerinsäure Mesoxalsäure Pd/C Pt/C Au/C Tartronsäure Sauerstoff Kohlenstoff Wasserstoff
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Fermentation of glycerol to 3-hydroxypropanal
Acrolein Biological pathway: Fermentation of glycerol to 3-hydroxypropanal Thermal reaction to acrolein Chemical pathway: heterogeneous (Y > 70 %) Solid acids (e.g. zeolites, H3PO4, Nafion) homogeneous (Y = -100 %) in scH2O Potential applications: Production of acrylic acid, methionine and glutaraldehyde
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Contents Glycerol Alkyl ethers Alkenyl ethers (telomers) Oligomers Polymers Oxidation products Carbonylation products Other derivatives
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Glycerincarbonylierung
[M]: Übergangsmetall- komplexe (Ir, Rh, …) Anwendungen: Polyester Harze ● ●
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Contents Glycerol Alkyl ethers Alkenyl ethers (telomers) Oligomers Polymers Oxidation products Carbonylation products Other derivatives
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Monoglycerides Transesterification Application: non-ionic surfactants Esterification catalysts: Faujasite, MCM-41, SBA-15 catalysts: ZnO, MgO
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Reaction with different aldehydes or ketones:
Acetals and Ketals Reaction with different aldehydes or ketones: formaldehyde acetone butyraldehyde catalyst: cation exchanger (Amberlyst 15) Change in solubility Potential applications: Ignition support for all types of combustion engines and antiknock additive
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1,3-Propanediol Biological pathway: enzymatic (Y > 85 %) with microorganisms (Y = 87%) Chemical pathway: heterogeneous (Y < 60 %) Supported metals (Re, Ru, Cu, …) or solid acids highly active but low selectivity homogeneous (Y < 70 %) Noble metals (e.g. Ru, Rh, Pt) Ligands containing P, As, Sb or CO Acids high selective but low activity Potential applications: Polymers, Solvents (esters)
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Dihydroxy- butanoic acid
Summary Glyceric acid GTBE Telomers Glycerol Oligomers Dihydroxy- butanoic acid Polymers
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