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Development of integrated bioprocess for ethanol production from sugar beet Dr. sc. Božidar Šantek, Full Professor Department of Biochemical Engineering, Faculty of Food Technology and Biotechnology, University of Zagreb, Pierotijeva 6/IV, HR-10000, Zagreb, Croatia bsantek@pbf.hr.
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Development of integrated bioprocess for ethanol production from sugar beet Dr. sc. Božidar Šantek, Full Professor Department of Biochemical Engineering, Faculty of Food Technology and Biotechnology, University of Zagreb, Pierotijeva 6/IV, HR-10000, Zagreb, Croatia bsantek@pbf.hr
Introduction- biofuels are viable and realistic alternative in the energy marketdue to rising environmental concerns and oil prices - biodiesel from plant oils and from animal waste fats - bioethanol from grains, sugar cane and sugar beet- bioethanol production from lignocellulose raw materials at the beginning of the large-scale commercialproduction (e.g. new plants in the USA)- the production costs of biofuels are higher than production costs of gasoline from fossil oil(e.g. gasoline is 2 times cheaper thanbioethanol)
LCA -bioethanol prodution from sugar beet Figure 1.General unit operations in bioethanol production from sugar beet.
Table 1.Unit operations incorporated in different ethanol production plants used for determination of total and specific area for embedding processes. (+) incorporated in the process; (-) not incorporated in the process; (*) the calculation with the 50 % of heat recuperation; (A) simultaneous sugar extraction, fermentation and product recovery.
Table 2. Total energy consumption for different processes of bioethanol production from sugar beet (1) Energy obtained from biogas counted in as goodness Figure 2.The ecological footprint (specific area; atot) of examined processes for ethanol production.
Experimental set-up of stirred tank bioreactor Sugar beet juice - addition of NH4H2PO4 as N and P suorce (1 g/L) - medium sterilization at 121 oC for 20 min prior to inoculation with yeast Saccharomyces cerevisiae - ethanol production in STB (5 L) at 28 oC with 10 % v/v yeast suspension - batch and fed batch cultivation techniques were used - pH value was maintained in the range of 4.5 - 5.0 by the addition of 0.1 M NaOH and 0.1 M H2SO4 - feeding in the fed batch process started when carbon source was almostcompletely depletedby the addition of a few portions of concentrated sugar beet juice (200 mL; approx. 800 g/L of sugar)
Figure 3.Alteration of substrate (S,●), ethanol (P1,▲) and glycerol (P2,∆) concentration during batch fermentation of raw sugar beet juice in stirred tank bioreactor
Figure 4.Alteration of substrate (S,■), ethanol (P1,▲), glycerol (P2, □) and biomass (X, ●) concentration, pH (○) and broth absorbance (A600nm,∆) during fed batch fermentation of raw sugar beet juice in stirred tank bioreactor. Arrows represent the addition of concentrated fresh medium during the fed batch process.
Experimental set-upof HRTB Sugar beet cossettes - ethanol production at room temperature after bioreactor sterilization at121 oC for 30 min. - 5 kg of non-sterile raw sugar beet cassettes (23 % dry matter) - addition of NH4H2PO4 (1 g/kg raw sugar beet cossettes) - inoculum Saccharomyces cerevisiae - different quantities of inoculum (9.1-23.7 % V/m of raw sugar beet cossettes)in order to define the broth minimal liquid content - different operational conditions of HRTB [rotation, the working volume of bioreactor (range 20 – 70 %)]
Figure 6. Alteration of substrate (S,●), ethanol (P1,▲), glycerol (P2,∆), acetate (P3,□) concentration and dry mass of sugar beet cossettes (DM,○) inside raw sugar beet cossettesduring fermentation in HRTB with the inoculum of 16.7 % V/mby periodical rotation
Figure 7. Alteration of substrate (S,●), ethanol (P1,▲), glycerol (P2,∆), acetate (P3,□) concentration in the liquidpart of the fermentation brothin the HRTB with inoculum of 16.7 % V/mby periodical rotation
Table 3. Comparison among different systems for ethanol production from intermediates of sugar beet processing RSBJ - raw sugar beet juice, RSBC - raw sugar beet cossettes, STB - stirred tank bioreactor, BP - batch process, FBP - fed batch process, INM - inoculum
Rotational set-up of HRTB during ethanol production from raw sugar beet cossettes Table 4. Investigation of the manner of HRTB rotation Table 5. Investigation of optimal rotation interval and speed of HRTB
Figure 8. Alteration of substrate (S,●), ethanol (P1,▲), glycerol (P2,∆), acetate (P3,□) concentration and dry mass of sugar beet cossettes (DM,○) inside raw sugar beet cossettesthe fermentation brothin HRTB with the inoculum of 16.7 % V/m by 3 min/h rotation and the rotation speed of 15 min-1
Figure 9. Alteration of substrate (S,●), ethanol (P1,▲), glycerol (P2,∆), acetate (P3,□) concentration in the liquid part of the fermentation brothin HRTB with the inoculum of 16.7 % V/mby 3 min/h rotation and the rotation speed of 15 min-1
Conclusions - sugar beet juice and cossettes can be successfully used for ethanol production. - the use of raw sugar beet cossettes in ethanol production eliminates extraction process of sugar beet cossettes by hot water, which considerably reduces energy demand for bioethanol production and final ethanol price. - further research of ethanol production from the raw sugar beet cossettes is required combined with improvement of sampling techniques due to the system heterogeneity