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Chapter 2: Biological Process for Ethanol Production

Chapter 2: Biological Process for Ethanol Production. By Dr Ku Syahidah Ku Ismail. Properties of Ethanol. Molecular formula CH 3 CH 2 OH Molecular weight 46.07 g/mol Density at 20 C 0.7893 kg/L Viscosity at 20C 1.2 cP Freezing point -114.3C Boiling point 78.4C.

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Chapter 2: Biological Process for Ethanol Production

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  1. Chapter 2:Biological Process for Ethanol Production By Dr Ku Syahidah Ku Ismail

  2. Properties of Ethanol • Molecular formula CH3CH2OH • Molecular weight 46.07 g/mol • Density at 20C 0.7893 kg/L • Viscosity at 20C 1.2 cP • Freezing point -114.3C • Boiling point 78.4C

  3. Ethanol as fuel Ethanol can be burned to form carbon dioxide and water, releasing energy: C2H5OH(g) + 3O2 (g) 2CO2(g) + 3H2O (l) G = -1409 kJ/mol

  4. Bioethanol Production Process

  5. Sugar-platform Bioethanol Production • From sugarcane, sugar beet, sweet sorghum. • Rich in sugars mainly sucrose

  6. Ways to obtain sugar from various raw materials SUGAR

  7. Saccharification and Hydrolysis for Fermentable Sugar Production

  8. Saccharification of Starch Degrade starch into oligosaccharides and dextrin Convert oligosaccharides and dextrin into glucose

  9. Composition of some biomass Chemical composition of biomass (adapted from Mosier et al., 2005).

  10. Schematic of goals of pretreatment on lignocellulosic material (adapted from Hsu et al., 1980).

  11. Hydrolysis of Lignocellulose

  12. Purposes of pretreatment • Helps in separation of main biomass components (cellulose, hemicellulose and lignin) • Increase available surface area • Reduce particle size • Ideally pretreatment: • Solubilizeshemicellulose • Increases enzymatic hydrolysibility of cellulose

  13. Ideal Pretreatment • Cheap • Fast • Robust • Simple • Catalyst recycling • Minimal environmental impact • Very good overall sugar recovery in hydrolysable and fermentable form • Generates minimum amount of degradation products

  14. Pretreatment – “Disruption” • Possible methods: • Mechanical • Milling (wet, dry) wet disc refining • Time consuming, intensive, expensive • Irradiation (microwave heating) • Slow, substrate specific, expensive • Chemical (acid and base) • Biological (white rot fungi) • Lignin-solubilizing microorganisms • No chemicals • Slow • Consumption of cellulose and hemicellulose • Combination (synergistic effects) • Chemical followed by biological • Physical followed by biological

  15. Pretreatments

  16. Basic structure of cellulose Cellulose is a long-chain homogeneous polysaccharide of D-glucose units, linked by β-1,4 glycosidic bonds. It is composed of over 10,000 glucose units.

  17. Quiz 1 • 1. What are the differences between hemicellulose and cellulose? • 2. Potatoes and sweet potatoes are excellent starch crops. Compare them with corn in starch production and as a feedstock for ethanol production.

  18. Physical Pretreatment

  19. Mechanical comminution • By chipping, grinding, milling to reduce cellulose crystallinity. • Size of material is usually 1 - 3 cm after chipping, and 0.2 – 2 mm after milling or grinding. • Vibratory ball milling is more effective than the ordinary ball milling.

  20. Steam explosion • Most commonly used methods for lignocellulosic materials • Chipped biomass is treated with high-pressure saturated steam and then the pressure is swiftly released, which makes the materials undergo an explosive decompression. • Carried out at 160 – 260 C (0.69 – 4.83 MPa) • It causes hemicellulose degradation and lignin transformation due to high temperature, thus increases the potential of cellulose hydrolysis. • Factors to consider during steam explosion pretreatment; residence time, temperature, chip size, moisture content • Addition of H2SO4 (or SO2) or CO2 in steam explosion can improve enzymatic hydrolysis, decrease inhibitory compounds and lead to more complete removal of hemicellulose.

  21. Steam explosion (cont.) • Optimal conditions of steam explosion pretreatment for sugarcane bagasse: temperature, 220C; residence time, 30 s; water-to-solid ratio, 2; H2SO4 dose, 1 g H2SO4 per 100 g dry bagasse. Based on this set condition, they got 65.1 g sugar/100 g starting bagasse after steam explosion pretreatment. • Advantages of steam explosion pretreatment: a) low energy requirement compared to mechanical comminution b) no recycling or environmental costs associated with chemical pretreatment c) the most cost-effective pretreatment processes for hardwoods and agricultural residues, but less effective for softwoods. • Limitations of steam explosion: a) destruction of a portion of xylan fraction b) incomplete disruption of lignin-carbohydrate matrix c) generation of inhibitory compounds in downstream processing

  22. Ammonia fiber explosion (AFEX) • Lignocellulosic material are exposed to liquid ammonia at high temperature for a period of time, and then flashed to a lower pressure. • The concept is similar to steam explosion. • A typical AFEX process: Dosage of liquid ammonia used is 1-2 kg ammonia/kg dry biomass; temperature 90C, residence time 30 min. • AFEX can significantly improve the saccharification rates of various herbaceous crops and grasses eg. alfalfa, wheat straw, corn stover, rice straw, switchgrass. • It was reported that over 90% hydrolysis of cellulose and hemicellulose was obtained after AFEX using bermudagrass and bagasse. • AFEX is not very effective for the lignocellulosic biomass with high lignin content such as newspaper (18-30% lignin) and wood chips (25-35% lignin).

  23. Ammonia fiber explosion (AFEX) (cont.) • To reduce the cost and protect the environment, ammonia needs to be recycled after the pretreatment. • AFEX did not produce inhibitors for the downstream biological processes, so water wash is not necessary. • AFEX pretreatment did not require small particle size for efficacy. • Cost of AFEX process is higher than steam explosion.

  24. Carbon dioxide explosion • Similar to steam and ammonia explosion • It was hypothesized that CO2 would form carbonic acid and increase the hydrolysis rate. • The yields are relatively low compared to steam explosion or AFEX, but high compared to the enzymatic without pretreatment. • CO2 explosion was more cost-effective than AFEX and did not form inhibitory compounds.

  25. Pyrolysis • Lignocellulosic materials are treated at temperature higher than 300C. • Cellulose would rapidly decompose to produce gaseous and tarry compounds.

  26. Chemical Pretreatment

  27. Ozonolysis • Ozone is used to degrade lignin and hemicellulose, while cellulose is hardly affected. • Advantages: a) it effectively removes lignin b) it does not produce toxic residues for the downstream processes c) the reactions are carried out at room temperature and pressure. • Disadvantage: A large amount of ozone is required in the process, making the process expensive.

  28. Acid Hydrolysis • Using concentrated acids such as H2SO4 and HCl • Dilute sulfuric acid pretreatment could achieve high reaction rates and significantly improve cellulose hydrolysis. • There are two types of dilute acid pretreatment process: High temperature (T > 160C), continuous-flow process for low solids loading (5%-10% [w/w]) Lower temperature (T < 160C), batch process for high solids loading (10%-40% [w/w]) • Cost is higher than steam explosion or AFEX. • A neutralization of pH is necessary before enzymatic hydrolysis or fermentation process.

  29. Alkaline Hydrolysis • Alkaline pretreatment can disrupt lignin structure and decrease crystallinity of cellulose and degree of sugar polymerization. • Compared with acid pretreatment, alkaline pretreatment has less sugar degradation and inhibitory compounds (furan derivatives) formation • NaOH and lime can be recovered or regenerated. • NaOH is very efficient in removing lignin from lignocellulosic materials at a temperature of 100C for 15-30 min. • Lime pretreatment of switchgrass at low temperature could significantly improve the sugar yield , but the time is longer (6 h).

  30. Oxidative delignification • Lignin biodegradation could be catalyzed by peroxidase enzyme with the presence of H2O2. • It was reported that about 50% lignin and most hemicellulose were solubilized by 2% H2O2 at 30C within 8 h.

  31. Organosolv Pretreatment • An organic or aqueous organic solvent mixture with inorganic acid catalyst (HCl or H2SO4) is used to break the internal lignin and hemicellulose bonds. • The organic solvents used include methanol, ethanol, acetone, ethylene glycol, triethylene glycol and tetrahydrofurfuryl alcohol. • At high temperature (T > 185C), the addition of catalyst is unnecessary. • Usually, a high yield of xylose can be obtained with the addition of acid. • Solvents used in the process need to be drained from the reactor, evaporated, condensed and recycled to reduce the cost. • Removal of solvents from the system is necessary because the solvents may be inhibitory to the growth of organisms.

  32. Biological Pretreatment • Microbes used: brown-, white-, and soft-rot fungi. • Brown rots mainly attack cellulose. • White and soft-rots attack both cellulose and lignin. • White-rot fungi are the most effective basidiomycetes for biological pretreatment of lignocellulosic materials. • The white-rot fungus Phanerochaetechrysosporiumproduces lignin-degrading enzymes, lignin peroxidases in response to carbon or nitrogen limitation. • Advantages of biological pretreatment: Low energy requirement and mild environmental conditions • Disadvantage of biological pretreatment: Rate of hydrolysis is very slow

  33. Fermentation Process • Using yeast or bacteria • In yeast fermentation, the glucose solution obtained from starch saccharification or cellulose hydrolysis is cooled to around 32C. • Yeast culture is added into the solution under aseptic condition • Glucose in the solution penetrates into the yeast cells through a series of enzymatic reactions to eventually ethanol, CO2 and energy. • Some of the released energy and glucose are utilized by the yeast cells to support their growth during fermentation. • The rest of the energy becomes heat to the fermentation broth and may increase the temperature if not taken out of the system. • Both ethanol and CO2 penetrate out of yeast cells. • CO2 readily dissolves in water, but can easily be saturated in fermentation broth. • The excess CO2 bubbles out of the liquid and can be collected for food and soft drink preparation.

  34. Fermentation Process (cont.) • Initially, yeast cell concentration is low and yeast growth is dominant • Glucose is mainly utilized to support the growth of yeast cells, so little ethanol and CO2 are produced and the glucose conversion rate is relatively low. • The length of initial stage depends on yeast inoculation ratio and the fermentation temperature. • At normal inoculation ratio (5-10%), 30C, it takes approximately 6-8 h. • Then the yeast cells will tremendously increase to over 108 cells/mL. • The fermentation becomes very active, resulting in rapid ethanol, CO2 and energy production, which is indicated by vigorous bubbling and heat production. • At this time, cooling is required to maintain the fermentation temperature at 30 C. • Active fermentation lasts about 12h, then the fermentation activity slows down because less glucose is available. • During the slow fermentation period, the yeast cells do not grow anymore, the biochemical reactions are limited by the substrate (glucose) concentration.

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