Abstract

The possibility of using waste distillery stillage (first-generation technology) after dilute acid pretreatment, as a medium for the preparation of beet molasses mash, for ethanol production according to the simultaneous saccharification and fermentation (SSF) technology, was assessed. The combination of lignocellulosic hydrolysates made from acid-pretreated stillage with sugar-rich beet molasses is an effective way of utilizing the first-generation ethanol production by-products in the second-generation ethanol production technology. It was demonstrated that the final ethanol concentration could be as high as 90 g/L. The process yield was over 94% of the theoretical yield when the molasses was diluted using acid-pretreated maize distillery stillage. An attempt to increase the pool of fermentable sugars by using cellulases to hydrolyze cellulose failed due to product inhibition in the fermentation medium with a high glucose concentration. A more than threefold increase in the concentration of ethyl acetate (even up to 924.4±11.8 mg/L) was observed in the distillates obtained from the media incubated with cellulases. The use of beet molasses combined with the hydrolysate of pretreated distillery stillage also changed the concentration of other volatile by-products. An increase in the concentration of aldehydes (mainly acetaldehyde to a concentration of above 1500 mg/L), methanol, 1-propanol, and 1-butanol was observed, while the concentration of higher alcohols (isobutanol, 2-methyl-1-butanol, 3-methyl-1-butanol) decreased. Interestingly, the use of cellulases in fermentation media from molasses and stillage hydrolysates resulted in an average fourfold increase in the concentration of this ester to a maximum level of 924.4±11.8 mg/L. Hydrolysates made from acid-pretreated distillery stillage, combined with sugar-rich beet molasses to boost the efficiency of the conversion process, can be successfully used in the production of second-generation fuel ethanol. However, further optimization of the cellulose enzymatic hydrolysis process is required for efficient use of the raw material.

Highlights

  • Second-generation bioethanol is an alternative to fossil fuels, and its production from lignocellulosic raw materials, which are waste from various branches of the agri-food and wood processing industries, does not pose a risk of rising food prices [1, 2]

  • The results demonstrated that in each experimental variant, it was possible to carry out an effective alcoholic fermentation in the media containing molasses and distillery stillage hydrolysates

  • In the first 48 h of the fermentation process, the rate of glucose and fructose uptake by yeast was similar in the media with only molasses, in the media with molasses and rye stillage hydrolysates, and in the variant supplemented with cellulases and maize stillage (Fig. 2c)

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Summary

Introduction

Second-generation bioethanol is an alternative to fossil fuels, and its production from lignocellulosic raw materials, which are waste from various branches of the agri-food and wood processing industries, does not pose a risk of rising food prices [1, 2]. In parallel to this process, the sugarcane bagasse is pretreated; e.g., with the use of dilute acids and increased pressure, cellulose is subjected to enzymatic hydrolysis for about 2–3 days, and the obtained hydrolysate is fermented Both technological lines meet at the stage of distillation and subsequent dehydration of ethanol [5]. Maize grain is used to produce ethanol from starch, while the stalks serve as lignocellulosic substrate Both technological lines meet at the fermentation stage, as the preparation of raw materials (grinding or pretreatment) and hydrolysis (mashing with the use of amylolytic enzymes and cellulose hydrolysis with cellulases) is carried out separately. The aim of such a technological line is to obtain a fermentation medium with an increased concentration of fermentable sugars (combination of starch and cellulose hydrolysate) and to reduce the concentration of inhibitors generated during the pretreatment of lignocellulose [20, 21]

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