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. 2019 Jul 4;24(13):2451.
doi: 10.3390/molecules24132451.

A Citrus Peel Waste Biorefinery for Ethanol and Methane Production

Affiliations

A Citrus Peel Waste Biorefinery for Ethanol and Methane Production

Maria Patsalou et al. Molecules. .

Abstract

This paper deals with the development of a citrus peel waste (CPW) biorefinery that employs low environmental impact technologies for production of ethanol and methane. Three major yeasts were compared for ethanol production in batch fermentations using CPW pretreated through acid hydrolysis and a combination of acid and enzyme hydrolysis. The most efficient conditions for production of CPW-based hydrolyzates included processing at 116 °C for 10 min. Pichia kudriavzevii KVMP10 achieved the highest ethanol production that reached 30.7 g L-1 in fermentations conducted at elevated temperatures (42 °C). A zero-waste biorefinery was introduced by using solid biorefinery residues in repeated batch anaerobic digestion fermentations achieving methane formation of 342 mL gVS-1 (volatile solids). Methane production applying untreated and dried CPW reached a similar level (339-356 mL gVS-1) to the use of the side stream, demonstrating that the developed bioprocess constitutes an advanced alternative to energy intensive methods for biofuel production.

Keywords: bioethanol; biomethane; biorefinery; biorefinery residues; citrus peel waste.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Process flow sheet of the zero-waste biorefinery used for citrus peel waste (CPW) valorization.
Figure 2
Figure 2
Εthanol titre achieved in Pichia kudriavzevii KVMP10, Saccharomyces cerevisiae, and Kluyveromyces marxianus fermentations of hydrolyzates obtained through dilute acid treatment of CPW.
Figure 3
Figure 3
Cumulative methane production using 6 gVS L−1 of untreated CPW (formula image), dried citrus peel waste (DCPW) (formula image), and solid biorefinery residues (BR) (formula image). A control fermentation was conducted without the addition of CPW (formula image), while all experiments were conducted at 37 °C. Dashed lines represent the time where substrate refeed was applied.
Figure 4
Figure 4
Concentration of volatile fatty acids, (A) formate, (B) propionate, (C) acetate, (D) butyrate, and (E) valerate, formed during anaerobic digestion of untreated CPW (formula image), DCPW (formula image), solid BR (formula image), and in the control experiment (formula image).
Figure 5
Figure 5
Yield of methane (A) as mL of product per g of initial volatile solids (VS) and (B) as mL of product per g of raw material (rm) generated from anaerobic digestion of CPW, DCPW, and BR following completion of each batch.
Figure 6
Figure 6
Cumulative methane production (A) and methane content per g of initial VS (B) using 3 g L−1 (formula image), 6 g L−1 (formula image), 12 g L−1 (formula image), and 24 g L−1 (formula image) initial volatile solids of CPW. A control fermentation was performed without the addition of CPW (formula image), while all experiments were conducted at 37 °C.

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