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Industries currently rely on chicory and Jerusalem artichoke for inulin extraction but also cardoon is proved to synthetize and store high quantity of inulin in roots as well. Cardoon is a multipurpose crop, well adapted to marginal lands, whose main residues at the end of cropping cycle consist of roots. However, cardoon roots are a suitable source of inulin, that is of high interest for new generation biodegradable bioplastics production. On the other hand, a sustainable supply chain for inulin production from cardoon roots has not been developed yet. In particular, in the inulin supply chain the most critical part is storage, which can negatively affect both cost and inulin quantity. In the present study the effect on inulin content in cardoon roots stored as dried chipped roots (CRt) and dried whole roots (WRt) was investigated in a 6-month storage trial. Our findings suggest that chipping before storage did not affect the inulin content during the storage. Furthermore, it reduced the time needed for drying by 33.3% and increased the bulk density by 154.9% with the consequent reduction of direct cost for drying, transportation and storage., This research was performed within the Italian Project COMETA-Autoctone Mediterranean crops and their valorization with advanced green chemistry technologies. The project was funded by Ministry of Education, Universities and Research in the frame of PON "Ricerca e Innovazione" 2014���2020 and FSC/ARS01_00606 COMETA/CUP. B2G18000180004/Azione II.

The present investigation aims at exploring the application of low-cost catalysts based on smectitic clays to the hydrodeoxygenation (HDO) of Cynara cardunculus derived lignin. Two types of clay minerals, montmorillonite and saponite, are pillared and decorated with suitable metals by means of an optimized process and characterized by X-ray powder diffraction (XRPD), porosity, scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), Fourier-transform infrared spectroscopy (FTIR), UV–vis–NIR, Raman, and thermogravimetric analysis (TGA). Alkaline lignin is obtained from steam-treated cardoon. Lignin depolymerization is conducted in a bench-scale apparatus under subcritical conditions, at relatively low temperature (320 °C), for 3 h, under 5-6 MPa of total pressure. Four catalysts are tested, namely, Fe/Al-pillared montmorillonite (FAMO) and saponite (FASA), and Ni-exchanged Ni/Al-pillared montmorillonite (Ni–Ni/AMO) and saponite (Ni–Ni/ASA). Results indicate that mineral clay–based catalysts result effectively in the hydrogenolysis of lignin, producing several low molecular weight aromatics and other species, with overall conversions in the range 60–70%. Montmorillonite-based catalysts yield the highest substrate conversion, with a prevalence of phenols and substituted phenols, whereas only Ni–Ni/ASA generates a higher abundance of aliphatic hydrocarbons. Overall, data indicate that smectitic clays are promising catalyst supports for products-oriented HDO of lignin.

Biomass-derived sugars are platform molecules that can be converted into a variety of final products. Non-food, lignocellulosic feedstocks, such as agroforest residues and low inputs, high yield crops, are attractive bioresources for the production of second-generation sugars. Biorefining schemes based on the use of versatile technologies that operate at mild conditions contribute to the sustainability of the bio-based products. The present work describes the conversion of giant reed (Arundo donax), a non-food crop, to ethanol and furfural (FA). A sulphuric-acid-catalyzed steam explosion was used for the biomass pretreatment and fractionation. A hybrid process was optimized for the hydrolysis and fermentation (HSSF) of C6 sugars at high gravity conditions consisting of a biomass pre-liquefaction followed by simultaneous saccharification and fermentation with a step-wise temperature program and multiple inoculations. Hemicellulose derived xylose was dehydrated to furfural on the solid acid catalyst in biphasic media irradiated by microwave energy. The results indicate that the optimized HSSF process produced ethanol titers in the range 43&ndash, 51 g/L depending on the enzymatic dosage, about 13&ndash, 21 g/L higher than unoptimized conditions. An optimal liquefaction time before saccharification and fermentation tests (SSF) was 10 h by using 34 filter paper unit (FPU)/g glucan of Cellic&reg, CTec3. C5 streams yielded 33.5% FA of the theoretical value after 10 min of microwave heating at 157 &deg, C and a catalyst concentration of 14 meq per g of xylose.

The use of low-cost substrates represents one key issue to make single cell oil production sustainable. Among low-input crops

The production of seed oils from Cynara cardunculus generates huge amounts of lignocellulosic residues which can be exploited according to a cascade approach. In this paper, residual cardoon biomass (RCB) was tested as a growth substrate for the solid-state production of cellulolytic cocktails by species known to produce glucose-tolerant β-glucosidase isoenzymes. Best productions were obtained with 10-d-old Aspergillus tubingensis cultures on RCB supplemented with wheat bran (200 g kg−1) yielding β-glucosidase and endo-β-1,4-glucanase activities as high as (25 and 4) IU g−1, respectively, and 4 FPU g−1. The saccharification performance of the obtained cocktail tested on acid-catalysed steam-exploded RCB at low solid loading (25 g dm−3) was around 53% at 20 FPU g−1 cellulose. These performance were significantly enhanced by adding the xylanase-rich NS 22083 commercial formulation, reaching glucose yields higher than 80% after 72 h incubation. The use of the catalytic additive was optimized by a statistical approach, based on factorial analysis. A comparison of the performance of the A. tubingensis reinforced cocktail with the Cellic®CTec2 taken as benchmark formulation was done at the same enzyme load and performed at industrially relevant solid loadings, namely at (100 and 200) g dm−3. This comparison showed that Cellic®CTec2 led to only slightly higher glucose yields while an opposite outcome was observed for xylose yields, irrespective of the solid loading conditions. Thus, this study shows that an in-house enzyme production, based on the solid-state conversion of an industrial byproduct, able of yielding cellulolytic cocktails with substantial saccharification performance is feasible.

Lignocellulosic biomass represents one of the most important feedstocks for future biorefineries, being a precursor of valuable bio-products, obtainable through both chemical and biological conversion routes. Lignocellulosic biomass has a complex matrix, which requires the careful development of multi-step approaches for its complete exploitation to value-added compounds. Based on this perspective, the present work focuses on the valorization of hemicellulose and cellulose fractionsof giant reed (Arundo donax L.) to give second-generation sugars, minimizing the formation of reaction by-products. The conversion of hemicellulose to xylose was undertaken in the presence of the heterogeneous acid catalyst Amberlyst-70 under microwave irradiation. The effect of the main reaction parameters, such as temperature, reaction time, catalyst, and biomass loadings on sugars yield was studied, developing a high gravity approach. Under the optimised reaction conditions (17 wt% Arundo donax L. loading, 160 &deg, C, Amberlyst-70/Arundo donax L. weight ratio 0.2 wt/wt), the xylose yield was 96.3 mol%. In the second step, the cellulose-rich solid residue was exploited through the chemical or enzymatic route, obtaining glucose yields of32.5 and56.2 mol%, respectively. This work proves the efficiency of this innovative combination of chemical and biological catalytic approaches, for the selective conversion of hemicellulose and cellulose fractions of Arundo donax L. to versatile platform products.

Agricultural by-products such as corn stover are considered strategic raw materials for the production of second-generation bioethanol from renewable and non-food sources. This paper describes the conversion of steam-pretreated corn stover to ethanol utilising a multi-step process including enzymatic hydrolysis, isomerisation, and fermentation of mixed hydrolysates with native Saccharomyces cerevisiae. An immobilised isomerase enzyme was used for the xylose isomerisation along with high concentrations of S. cerevisiae. The objective was to assess the extent of simultaneity of the various conversion steps, through a detailed analysis of process time courses, and to test this process scheme for the conversion of lignocellulosic hydrolysates containing several inhibitors of the isomerase enzyme (e.g. metal ions, xylitol and glycerol).The process was tested on two types of hydrolysate after acid-catalysed steam pretreatment: (a) the water soluble fraction (WSF) in which xylose was the largest carbon source and (b) the entire slurry, containing both cellulose and hemicellulose carbohydrates, in which glucose predominated.The results indicated that the ethanol concentration rose when the inoculum concentration was increased in the range 10-75g/L. However, when xylose was the largest carbon source, the metabolic yields were higher than 0.51gethanol/gconsumed sugars probably due to the use of yeast internal cellular resources. This phenomenon was not observed in the fermentation of mixed hydrolysates obtained from the entire pretreated product and in which glucose was the largest carbon source. The ethanol yield from biomass suspensions with dry matter (DM) concentrations of 11-12% (w/v) was 70% based on total sugars (glucose, xylose, galactose). The results suggest that xylulose uptake was more effective in mixed hydrolysates containing glucose levels similar to, or higher than, xylose.Analysis of the factors that limit isomerase activity in lignocellulosic hydrolysates excluded any inhibition due to residual calcium ions after the detoxification of the hemicellulose hydrolysates with Ca(OH)2. By contrast, most of the enzyme activity ceased during the fermentation of the entire slurry after steam explosion, probably due to synergistic inhibition effects of various fermentation co-products. © 2014 Elsevier B.V.

Fuel grade bioethanol can be produced from a number of lignocellulosic biomass sources. In the present paper the enzymatic hydrolysis of giant reed (Arundo donax) at high biomass loadings up to 20% (w/v) was investigated. Two pretreatment technologies were used: one step steam explosion (SE) with and without acid catalyst and the novel pilot process from Chemtex consisting in a two steps pretreatment. The results of the biomass composition after different pretreatment conditions along with the corresponding enzymatic hydrolizability at low solids loading, indicated that the best pretreatments were the acid catalyzed steam explosion (ACSE) at 200 °C and the Chemtex process in which the SE step was carried out at 206 for 4. min. Various process configurations, including biomass and enzymes fed-batch, were investigated to avoid excessive viscosities and increase the cellulose conversion. Novel enzymatic preparations from Novozymes, Cellic™ Ctec1 and Cellic™ Ctec2, were used for the biomass saccharification. Concerning the analysis of the factors that limited the hydrolysis yields at high DM content, some evidences indicated that product inhibition by xylooligomers could have an important role. The highest solids loading investigated in the present paper was 21%. Under these conditions and by using an enzymes loading of 0.28. g Ctec2/g glucan, an overall sugars concentration of 91. g/L (glucose. +. xylose) can be obtained after 48. h from ACSE at 200 °C. © 2012 Elsevier Ltd.

Bioethanol can be produced from several biomasses including lignocellulosic materials. Besides 6-carbon sugars that represent the prevalent carbohydrates, some of these feedstocks contain significant amounts of 5-carbon sugars. One common limit of the major part of the xylose-fermenting yeasts is the diauxic shift between the uptake of glucose and xylose during the fermentation of mixed syrups. Thus, optimized fermentation strategies are required.In this paper the ability of Scheffersomyces stipitis strain NRRLY-11544 to ferment mixed syrups with a total sugar concentration in the range 40-80. g/L was investigated by using mono cultures, co-cultures with Saccharomyces cerevisiae strain Bakers Yeast Type II and single cultures immobilized in silica-hydrogel films. The experimental design for the fermentations with immobilized cells included the process analysis in function of two parameters: the fraction of the gel in the broth and the concentration of the cells loaded in the gel. Furthermore, for each total sugars level, the fermentative course of S. stipitis was analyzed at several glucose-to xylose ratios.The results indicated that the use of S. stipitis and S. cerevisiae in free co-cultures ensured faster processes than single cultures of S. stipitis either free or immobilized. However, the rapid production of ethanol by S. cerevisiae inhibited S. stipitis and caused a stuck of the process.Immobilization of S. stipitis in silica-hydrogel increased the relative consumption rate of xylose-to-glucose by 2-6 times depending on the composition of the fermentation medium. Furthermore the films performances appeared stable over three weeks of continuous operations. However, on the whole, the final process yields obtained with the immobilized cells were not meaningfully different from that of the free cells. This was probably due to concurrent fermentations operated by the cells released in the broth. Optimization of the carrier characteristics could improve the performances of the process with immobilized cells. © 2013 Elsevier B.V.