Upgraded biofuel from residue biomass by Thermo-Catalytic Reforming and hydrodeoxygenation

Research is focused on the utilisation of waste or residue biomass for bioenergy conversion. A promising conversion technology for the production of liquid biofuels from residue biomass is a process called Thermo-Catalytic Reforming (TCR^®​) which is a combination of prior thermal treatment of the biomass at mild temperatures (intermediate pyrolysis) followed by a second catalytic treatment step at elevated temperatures (reforming). This article focuses on the conversion of TCR^® liquids from digestate as a feedstock for subsequent hydrocarbon production. The generated bio-oil showed a lower heating value of 34.0 MJ kg⁻¹ with an oxygen content of 7.0% and a water content of 2.2%. The bio-oil was hydrodeoxygenated using an industrial NiMo–Al₂O₃ catalyst at temperatures of 503 K–643 K and a pressure of 14 MPa. The hydrodeoxygenated bio-oil reached a lower heating value of 42.3 MJ kg⁻¹ with an oxygen content below 0.8 mg kg⁻¹ and water content of 30 ppm. Product yields and catalyst life give confidence that upgrading of the TCR^®​ bio-oil offers a suitable option to meet the high standards of common fuels.     

Combined ethanol and methane production from switchgrass (Panicum virgatum L.) impregnated with lime prior to steam explosion

Pretreatments are crucial to achieve efficient conversion of lignocellulosic biomass to soluble sugars. In this light, switchgrass was subjected to 13 pretreatments including steam explosion alone (195 °C for 5, 10 and 15 min) and after impregnation with the following catalysts: Ca(OH)₂ at low (0.4%) and high (0.7%) concentration; Ca(OH)₂ at high concentration and higher temperature (205 °C for 5, 10 and 15 min); H₂SO₄ (0.2% at 195 °C for 10 min) as reference acid catalyst before steam explosion. Enzymatic hydrolysis was carried out to assess pretreatment efficiency in both solid and liquid fraction. Thereafter, in selected pretreatments the solid fraction was subjected to simultaneous saccharification and fermentation (SSF), while the liquid fraction underwent anaerobic digestion (AD). Lignin removal was lowest (12%) and highest (35%) with steam alone and 0.7% lime, respectively. In general, higher cellulose degradation and lower hemicellulose hydrolysis were observed in this study compared to others, depending on lower biomass hydration during steam explosion. Mild lime addition (0.4% at 195 °C) enhanced ethanol in SSF (+28% than steam alone), while H₂SO₄ boosted methane in AD (+110%). However, methane represented a lesser component in combined energy yield (ethanol, methane and energy content of residual solid). Mild lime addition was also shown less aggressive and secured more residual solid after SSF, resulting in higher energy yield per unit raw biomass. Decreased water consumption, avoidance of toxic compounds in downstream effluents, and post process recovery of Ca(OH)₂ as CaCO₃ represent further advantages of pretreatments involving mild lime addition before steam explosion.     

Sunflower as a biofuels crop: An analysis of lignocellulosic chemical properties

Four accessions of cultivated sunflower (Helianthus annuus) and silverleaf sunflower (Helianthus argophyllus), were each grown in three locations (Georgia, British Columbia, and Iowa) at different planting densities and phenotyped for biomass-related traits and wood biochemistry. In most environments, H. argophyllus produced significantly more biomass than H. annuus. Cell wall chemistry for a subset of plants grown in Georgia and Iowa was assessed using analytical wet chemistry methods to measure lignin and sugar content/composition. The analysis of lignin and the S/G-lignin ratios for a larger number of samples (n > 250) was also assessed by high-throughput pyrolysis Molecular Beam Mass Spectrometry. Average pyMBMS estimated lignin content (i.e., dry weight fraction) for 60 °C dried basal stem samples of H. annuus and H. argophyllus was 29.6% (range, 24.0%–34.6%) and 28.6% (range, 24.6%–33.3%), respectively when averaged across all environments. The average S/G lignin mass ratio was 1.5 (range, 1.0–2.0) for H. annuus and 1.7 (range, 1.0–2.4) in H. argophyllus. Stem samples from these two species only differed statistically for a few cell wall chemistry traits; however, accession level differences within each species were apparent. Cell wall chemistry in both species was significantly affected by both location and planting density, thus demonstrating the need to select for these traits in the environment for which the crop will be produced. Overall, these results show that cultivated sunflower and silverleaf sunflower both possess the necessary phenotypic diversity to facilitate the development of a hybrid sunflower with improved lignocellulosic biofuels traits, namely increased biomass, decreased lignin, and increased glucan.     

Evaluation of dilute acid and alkaline pretreatments,enzymatic hydrolysis and fermentation of napiergrass for fuel ethanol production

Napiergrass (Pennisetum purpureum Schum.) is a promising low cost raw material which does not compete with food prices, has attractive yields and an environmentally friendly farming. Dilute sulfuric acid pretreatment of napiergrass was effective to obtain high yields of sugars and low level of degradation by-products from hemicellulose. Detoxification with Ca(OH)₂ removed inhibitors but showed sugars loss. An ethanol concentration of 21 g/L after 176 h was found from the hydrolyzate using Pichia stipitis NBRC 10063 (fermentation efficiency 66%). An additional alkaline pretreatment applied to the solid fraction remaining from the diluted acid pretreatment improved the lignin removal. The highest cellulose hydrolysis values were found with the addition of β-glucosidase and PEG 6000. The simultaneous hydrolysis and fermentation of the cellulosic fraction with Saccharomyces cerevisiae, 10% (w/v) solid concentration, β-glucosidase and PEG 6000, showed the highest ethanol concentration (24 g/L), and cellulose hydrolysis values (81%). 162 L ethanol/t of dry napiergrass were produced (overall efficiency of 52%): 128 L/t from the cellulosic fraction and 34 L/t from the hemicellulosic fraction.     

Sweet sorghum as a whole-crop feedstock for ethanol production

The potential of sweet sorghum as an alternative crop for ethanol production was investigated in this study. Initially, the enzymatic hydrolysis of sorghum grains was optimized, and the hydrolysate produced under optimal conditions was used for ethanol production with an industrial strain of Saccharomyces cerevisiae, resulting in an ethanol concentration of 87 g L⁻¹. From the sugary fraction (sweet sorghum juice), 72 g L⁻¹ ethanol was produced. The sweet sorghum bagasse was submitted to acid pretreatment for hemicellulose removal and hydrolysis, and a flocculant strain of Scheffersomyces stipitis was used to evaluate the fermentability of the hemicellulosic hydrolysate. This process yielded an ethanol concentration of 30 g L⁻¹ at 23 h of fermentation. After acid pretreatment, the remaining solid underwent an alkaline extraction for lignin removal. This partially delignified material, known as partially delignified lignin (PDC), was enriched with nutrients in a solid/liquid ratio of 1 g/3.33 mL and subjected to simultaneous saccharification and fermentation (SSF) process, resulting in an ethanol concentration of 85 g L⁻¹ at 21 h of fermentation. Thus, from the conversion of starchy, sugary and lignocellulosic fractions approximately 160 L ethanol.ton⁻¹ sweet sorghum was obtained. This amount corresponds to 13,600 L ethanol.ha⁻¹.     

An oil palm-based biorefinery concept for cellulosic ethanol and phytochemicals production: Sustainability evaluation using exergetic life cycle assessment

In this study, thermo-environmental sustainability of an oil palm-based biorefinery concept for the co-production of cellulosic ethanol and phytochemicals from oil palm fronds (OPFs) was evaluated based on exergetic life cycle assessment (ExLCA). For the production of 1 tonne bioethanol, the exergy content of oil palm seeds was upgraded from 236 MJ to 77,999 MJ during the farming process for OPFs production. Again, the high exergy content of the OPFs was degraded by about 62.02% and 98.36% when they were converted into cellulosic ethanol and phenolic compounds respectively. With a total exergy destruction of about 958,606 MJ (internal) and 120,491 MJ (external or exergy of wastes), the biorefinery recorded an overall exergy efficiency and thermodynamic sustainability index (TSI) of about 59.05% and 2.44 per tonne of OPFs' bioethanol respectively. Due to the use of fossil fuels, pesticides, fertilizers and other toxic chemicals during the production, the global warming potential (GWP = 2265.69 kg CO₂ eq.), acidification potential (AP = 355.34 kg SO₂ eq.) and human toxicity potential (HTP = 142.79 kg DCB eq.) were the most significant environmental impact categories for a tonne of bioethanol produced in the biorefinery. The simultaneous saccharification and fermentation (SSF) unit emerged as the most exergetically efficient (89.66%), thermodynamically sustainable (TSI = 9.67) and environmentally friendly (6.59% of total GWP) production system.     

Fuel properties of Brassica juncea oil methyl esters blended with ultra-low sulfur diesel fuel

Brassica juncea is a drought-tolerant member of the Brassicaceae plant family with high oil content and a short growing season that is tolerant of low quality soils. It was investigated as a feedstock for production of biodiesel along with evaluation of subsequent fuel properties, both neat and in blends with petroleum diesel fuel. These results were compared against relevant fuel standards such as ASTM D6751, EN 14214, ASTM D975, EN 590, and ASTM D7467. Crude B. juncea oil was extracted from unconditioned seeds utilizing a continuous tubular radial expeller. The oil was then chemically refined via degumming, neutralization and bleaching to render it amenable to direct homogeneous sodium methoxide-catalyzed transesterification. The principal fatty acid detected in B. juncea oil was erucic acid (44.1%). The resulting biodiesel yielded fuel properties compliant with the biodiesel standards with the exception of oxidative stability and kinematic viscosity in the case of EN 14214. Addition of tert-butylhydroquinone and blending with soybean oil-derived biodiesel ameliorated these deficiencies. The fuel properties of B5 and B20 blends of B. juncea oil methyl esters (BJME) in ultra-low sulfur (<15 ppm S) diesel (ULSD) fuel were within the ranges specified in the petrodiesel standards ASTM D975, EN 590 and ASTM D7467 with the exception of derived cetane number in the case of EN 590. This deficiency was attributed to the inherently low cetane number of the certification-grade ULSD, as it did not contain performance-enhancing additives. In summary, this study reports new fuel property data for BJME along with properties of B5 and B20 blends in ULSD. Such results will be useful for the development of B. juncea as an alternative source of biodiesel fuel.     

Simultaneous enzymatic saccharification and ABE fermentation using pretreated oil palm empty fruit bunch as substrate to produce butanol and hydrogen as biofuel

Simultaneous saccharification and acetone–ethanol–butanol (ABE) fermentation was conducted in order to reduce the number of steps involved in the conversion of lignocellulosic biomass into butanol. Enzymatic saccharification of pretreated oil palm empty fruit bunch (OPEFB) by cellulase produced 31.58 g/l of fermentable sugar. This saccharification was conducted at conditions similar to the conditions required for ABE fermentation. The simultaneous process by Clostridium acetobutylicum ATCC 824 produced 4.45 g/l of ABE with butanol concentration of 2.75 g/l. The butanol yield of 0.11 g/g and ABE yield of 0.18 g/g were obtained from this simultaneous process as compared to the two-step process (0.10 g/g of butanol yield and 0.14 g/g of ABE yield). In addition, the simultaneous process also produced higher cumulative hydrogen (282.42 ml) than to the two-step process (222.02 ml) after 96 h of fermentation time. This study suggested that the simultaneous process has the potential to be implemented for the integrated production of butanol and hydrogen from lignocellulosic biomass.     

Steam explosion pretreatment and enzymatic saccharification of duckweed (Lemna minor) biomass

Our previous research has shown that duckweed is potentially an ideal feedstock for the production of biofuels because it can be effectively saccharified enzymatically. Here we report the results of experiments in which duckweed was pre-treated by steam explosion prior to enzyme digestion. A range of temperatures, from 130 to 230 °C with a fixed retention time of 10 min, were employed. The best pretreatment conditions were 210 °C for 10 min; these conditions produced the highest amount of water-soluble material (70%), the greatest levels of starch solubilisation (21%) and hemicellulose and pectic polysaccharides degradation (60%). The use of these steam explosion conditions enabled large reductions in the concentrations of enzymes required for effective saccharification. The amount of Celluclast required was reduced from 100 U (4.35 FPU) g⁻¹ substrate to 20 U g⁻¹ substrate, and additional beta-glucosidase was reduced from 100 to 2 U g⁻¹ substrate.     

Evaluation of green solvents for a sustainable zein extraction from ethanol industry DDGS

Corn-ethanol industry in US alone generates about 35 Tg of Dried Distillers Grains with Solubles (DDGS) per year as co-product. DDGS is enriched with zein, a well-known corn protein. Vast potential of zein application in industries ranging from pharmaceuticals to bio-plastics resulted in a serious quest to develop process technologies for its extraction. A broad spectrum of primary, binary, ternary and tertiary solvents is available which can extract zein from DDGS. But most organic solvents are hazardous which limits their sustainable industrial-scale use. Our study evaluated green solvents: isopropanol, n-butanol, isobutanol, 2,3-butanediol (2,3-BDO), 1,4-butanediol, isoamyl alcohol, 1,3-dioxolane, 1,4-dioxane, tetrahydrofuran, acetic acid, lactic acid and ionic liquids [emim]Ac and [emim]Br for zein extraction. Isopropanol, 1,4-dioxane and 2,3-BDO showed promising results, with 75, 41 and 38% extraction efficiency, respectively. Operational parameters for efficient extraction such as temperature, pH and solvent-to-water ratio were subsequently optimized using response surface methodology for selected solvents. A combination of solvent to water volume ratio of 66:34, temperature of 77 °C and pH of 4.4 was found to be optimal for isopropanol, whereas 2,3-BDO worked best at solvent to water volume ratio of 73: 27, temperature of 85 °C and pH of 3.8. These results are encouraging and could lead to the development of green technology for efficient zein extraction.     

Anaerobic digestion of maize and cellulose under thermophilic and mesophilic conditions – A comparative study

The aim of this study was to advance in understanding of digestion process of energy crops. Cellulose and maize silage were fermented in batch mode at mesophilic (38 °C) and thermophilic (55 °C) conditions and corresponding organic loads of 5.5 ± 0.2 kgVS/m³, 11.2 ± 0.3 kgVS/m³ and 16.7 ± 0.4 kgVS/m³.For both substrates more stable and faster digestion took place at 38 °C. Due to complex structure maize degradation was characterized by varying digestion rate and longer total digestion time resulting form breakdown of hard-degradable fractions. The digestion retard at increased OLRs of cellulose and lower degradation level obtained for all cellulose series confirm a higher overloading potential for systems dealing with single-component-substrates but also the enhanced sensitivity of such systems to any inconvenient digestion conditions.Based on observed patterns of volatile fatty acids and oxidation-reduction potential, different fermentation mechanisms can be concluded for cellulose and maize, but also for different temperature modes. Conversion of maize at highly reductive conditions with increased concentrations of butyric acid was accompanied by much higher activity of hydrogenotrophic methanogens than for cellulose digestion.Two factors showed a strong potential to influence test results: an insufficient VS content of inoculum, which caused reduced biogas yields, and a high natural biodiversity of maize silage, resulting in higher biogas yields than calculated based on the maize composition.     

Biosynthesis of β-caryophyllene,a novel terpene-based high-density biofuel precursor,using engineered Escherichia coli

β-caryophyllene is a common sesquiterpene compound currently being studied as a promising precursor for the production of high-density fuels. Acute demand for high-density fuels has provided the impetus to pursue biosynthetic methods to produce β-caryophyllene from reproducible sources. In this study, we produced β-caryophyllene by assembling a biosynthetic pathway in an engineered Escherichia coli strain of which phosphoglucose isomerase gene has been deleted. The 1- deoxy-d-xylulose 5-phosphate (DXP) or heterologous mevalonate (MVA) pathways were employed. Meanwhile, geranyl diphosphate synthase, glucose-6-phosphate dehydrogenase and β-caryophyllene synthase genes were co-overexpressed in the above strain. The final genetically modified strain, YJM59, produced 220 ± 6 mg/L of β-caryophyllene in flask culture. We also evaluated the use of fed-batch fermentation for the production of β-caryophyllene. After induction for 60 h, the YJM59 strain produced β-caryophyllene at a concentration of 1520 mg/L. The volumetric production fermented in the aerobic fed-batch was 0.34 mg/(L·h·OD₆₀₀) and the conversion efficiency of glucose to β-caryophyllene (gram to gram) was 1.69%. Our results are the first successful attempt to produce β-caryophyllene using E. coli BL21(DE3), and provide a new strategy that is green and sustainable for the production of β-caryophyllene.     

Supercritical water gasification of timothy grass as an energy crop in the presence of alkali carbonate and hydroxide catalysts

This study is focused on identifying the candidature of timothy grass as an energy crop for hydrogen-rich syngas production through supercritical water gasification. Timothy grass was gasified in supercritical water to investigate the impacts of temperature (450–650 °C), biomass-to-water ratio (1:4 and 1:8) and reaction time (15–45 min) in the pressure range of 23–25 MPa. The impacts of carbonate catalysts (e.g., Na₂CO₃ and K₂CO₃) and hydroxide catalysts (e.g., NaOH and KOH) at variable mass fractions (1–3%) were examined to maximize hydrogen yields. In the non-catalytic gasification of timothy grass, highest hydrogen (5.15 mol kg⁻¹) and total gas yields (17.2 mol kg⁻¹) with greater carbon gasification efficiency (33%) and lower heating value (2.21 MJ m⁻³) of the gas products were obtained at 650 °C with 1:8 biomass-to-water ratio for 45 min. However, KOH at 3% mass fraction maximized hydrogen and total gas yields up to 8.91 and 30.6 mol kg⁻¹, respectively. Nevertheless, NaOH demonstrated highest carbon gasification efficiency (61.3%) and enhanced lower heating value of the gas products (4.68 MJ m⁻³). Timothy grass biochars were characterized through Fourier transform infrared spectroscopy, Raman spectroscopy and scanning electron microscopy to understand the behavior of the feedstock to rising temperature and reaction time. The overall findings suggest that timothy grass is a promising feedstock for hydrogen production via supercritical water gasification.     

Development of novel Ag/bauxite nanocomposite as a heterogeneous catalyst for biodiesel production

Ag/bauxite nanocomposites have been prepared using in situ reduction of aqueous AgNO₃ solution in a bauxite matrix and investigated for the transesterification of sunflower oil with methanol in order to study their potential as heterogeneous catalysts. The prepared nanocopmosites were characterized by XRD, SEM, EDX, FT-IR, and TG- DTA. The Central Composite Design of the Response Surface Methodology was used to optimize the effect of reaction temperature, reaction time, catalyst loading and methanol to oil molar ratio on the yield of fatty acid methyl esters. The highest yield was obtained at 67 °C reaction temperature, 3 h reaction time, 0.3 wt.% catalyst loading and 9:1 methanol to oil molar ratio. Under the optimal conditions, the methyl ester content was 94% and the catalyst successfully reused for at least 7 cycles without significant deactivation.     

Enhanced substrate degradation and methane yield with maleic acid pre-treatments in biomass crops and residues

Organic acids are envisaged as alternative catalysts to strong mineral acids, in pre-treatment of ligno-cellulosic biomass for anaerobic digestion (AD). To evaluate this hypothesis, an untreated control and four pre-treatments (25 °C for 24 h) involving two levels of maleic acid (34.8 and 69.6 kg m⁻³), alone and combined with sulphuric acid (4 kg m⁻³), were studied in three agricultural substrates: Arundo (aka giant reed), Barley straw and B133 fibre sorghum. Methane production was assessed in a batch AD assay (35 °C for 51 days) with 4 g L⁻¹ of volatile solid (VS) load. Fibre composition and structure were investigated through chemical analysis and Fourier transform infrared (FTIR) spectrometry. Arundo and B133 that were the most and least recalcitrant substrate, respectively, staged the highest and lowest increase in methane with high maleic acid: +62% over 218 cm³ g⁻¹ of VS in untreated Arundo; +36% over 284 cm³ g⁻¹ of VS in untreated B133. Barley straw showed an intermediate behaviour (+41% over 269 cm³ g⁻¹ of VS). H₂SO₄ addition to maleic acid did not improve CH₄ output. The large increase in methane yield determined by pre-treatments was reflected in the concurrent decrease of fibre (between 14 and 39% depending on fibrous component). Based on FTIR spectra, bands assigned to hemicellulose and cellulose displayed lower absorbance after pre-treatment, supporting the hypothesis of solubilisation of structural carbohydrates and change in fibre structure. Hence, maleic acid was shown a suitable catalyst to improve biodegradability of ligno-cellulosic biomass, especially in recalcitrant substrates as Arundo.     

Growth of microalgae using CO2 enriched air for biodiesel production in supercritical CO2

The optimum conditions for lipids productivity and CO₂ fixation of two freshwater strains, namely Chlorella sp. and Pseudochlorococcum sp. and a marine strain; namely Nannochlorpsis sp. have been determined in this work. The species were grown autotrophically under aeration with different CO₂ concentrations, ranging from 0.04 to 2% (v/v). The growth was tested in nitrogen sufficient and deficient media at different salinities (0.49–680 mM) and temperatures of 27 and 31 °C. The optimum CO₂ enrichment was found to be 1% (v/v) in both media. Nitrogen starvation resulted in an increase in lipid contents, but at lower growth rate, which resulted in a lower overall lipid productivity. The experimental data were used to determine the kinetic parameters of Haldane model. The Chlorella sp. grew well at salinity levels of up to 460 mM. The highest CO₂ biofixation rate was observed when Chlorella sp. was grown at 27 °C in seawater (230 mM NaCl).Lipids were extracted from harvested marine strain, Nannochlorpsis sp., and enzymatically transesterified to produce biodiesel in supercritical CO₂ (SC–CO₂) medium. It was found that the conversion of biodiesel produced from microalgae lipids was 35% higher than that achieved using lamb fat in a similar system.     

Physicochemical characterization and enzymatic digestibility of Chinese pennisetum pretreated with 1-ethyl-3-methylimidazolium acetate at moderate temperatures

1-ethyl-3-methylimidazolium acetate ([EMIM] AC) pretreatment at moderate temperatures (60 °C and 75 °C) was evaluated for improving hydrolysability of Chinese pennisetum, a leading candidate as an energy crop, for bioethanol production. The pretreatment caused slight carbohydrate and lignin loss but significantly changed the material physicochemical characters, such as crystallinity and surface structure. Both changes exhibited positive effects on improving the enzymatic digestibility of the Chinese pennisetum. It was observed that approximately 90% of the cellulose and 50% of the xylan in the Chinese pennisetum after pretreatment at 75 °C were converted to fermentable monosaccharides by the combined cellulases and endo-xylanase. The results suggested that Chinese pennisetum could be effectively pretreated with ([EMIM] AC) pretreatment at moderate temperatures, and the high hydrolysis yield of fermentable sugars from pretreated Chinese pennisetum could be achieved by the synergistic action of accessory xylanase in enzymatic hydrolysis by cellulases.     

Mild alkaline pre-treatments loosen fibre structure enhancing methane production from biomass crops and residues

Three ligno-cellulosic substrates representing varying levels of biodegradability (giant reed, GR; fibre sorghum, FS; barley straw, BS) were combined with mild alkaline pre-treatments (NaOH 0.05, 0.10 and 0.15 N at 25 °C for 24 h) plus untreated controls, to study pre-treatment effects on physical-chemical structure, anaerobic digestibility and methane output of the three substrates. In a batch anaerobic digestion (AD) assay (58 days; 35 °C; 4 g VS l⁻¹), the most recalcitrant substrate (GR) staged the highest increase in cumulative methane yield: +30% with NaOH 0.15 N over 190 ml CH₄ g⁻¹ VS in untreated GR. Conversely, the least recalcitrant substrate (FS) exhibited the lowest gain (+10% over 248 ml CH₄ g⁻¹ VS), while an intermediate behaviour was shown by BS (+15% over 232 ml CH₄ g⁻¹ VS). Pre-treatments speeded AD kinetics and reduced technical digestion time (i.e., the time needed to achieve 80% methane potential), which are the premises for increased production capacity of full scale AD plants. Fibre components (cellulose, hemicellulose and acid insoluble lignin determined after acid hydrolysis) and substrate structure (Fourier transform infra-red spectroscopy and scanning electron microscopy) outlined reductions of the three fibre components after pre-treatments, supporting claims of loosened binding of lignin with cellulose and hemicellulose. Hence, mild alkaline pre-treatments were shown to improve the biodegradability of ligno-cellulosic substrates to an extent proportional to their recalcitrance. In turn, this contributes to mitigate the food vs. fuel controversy raised by the use of whole plant cereals (namely, maize) as feedstocks for biogas production.     

Energy recovery from grass of urban roadside verges by anaerobic digestion and combustion after pre-processing

Grass from urban roadside verges is a potential, though widely unused, resource for bioenergy recovery. Two possible bioenergy recovery techniques were tested, i.e. i) direct anaerobic digestion of the whole parent material and ii) the “integrated generation of solid fuel and biogas from biomass” (IFBB) procedure, which divides biomass into a press fluid and a press cake by mashing and mechanical dewatering. Biomass yield, chemical composition and canopy height of biomass, contribution of functional groups, fermentation characteristics of silage and press fluids, as well as characteristics of the produced solid fuel was investigated, applying a 4-cut management for anaerobic digestion, a 2-cut management for IFBB and an 8 times mulching as a reference. Mean annual biomass yield (2013 and 2014) was 3.24, 3.33 and 5.68 t dry matter ha⁻¹ for the mulching, 4-cut management and 2-cut management, respectively. Yields were higher in 2014 due to more favourable weather conditions. Fibre concentration was higher in material of the 2-cut management than in the 4-cut management, however, methane yield of the corresponding silages was the same. Highest methane yield was gained from press fluids with 292 l_N kg⁻¹ volatile solids. The press cake had a lower heating value of 16 MJ kg⁻¹ dry matter and a K₂O/CaO index of 0.51–0.88. Gross energy output was 26.4 GJ ha⁻¹ for anaerobic digestion and 84.4 GJ ha⁻¹ for IFBB. Thus, an altered roadside verge management with reduced cutting frequency might allow a significant energy recovery and improved ecosystem services, i.e. increased biodiversity.     

Growth,yield, fiber content and lodging resistance in eight varieties of Cenchrus purpureus (Schumach.) Morrone intended as energy crop

Growth, biomass yield, fiber content and lodging resistance were studied, during a six month growth period, for eight varieties of Cenchrus purpureus, intended as energy crop, in Veracruz, Mexico. Then, only yield at day 182 was assessed for two additional years. The varieties were: CT115 (CT), African Cane (AC), Taiwan (TAI), King Grass (KG), Vruckwona (VRU), Roxo (RX), OM22 (OM) and Cameroon (CAM). Local weather is warm and sub-humid, historical data for monthly average temperature and annual rainfall were 25.8 °C and 1142 mm, respectively. Height, diameter and light interception were measured monthly from day 65–185. At day 185, biomass yield and tiller density were measured. Number of lying tillers was counted to estimate lodging resistance. Cellulose and hemicellulose content were estimated in leaf and stem. No differences were found for dry matter yield or stem yield at day 185 in the first year. Regarding the next two years, TAI yielded above CT, OM or ROX. Average dry matter yield was higher in the second year than in the establishment cycle (38.6 vs 21.1 Mg ha⁻¹), but decreased in the third year (32.2 Mg ha⁻¹). In both stem and whole plant, AC and KG showed higher hemicellulose content than RX, OM or CT; while AC and VRU had higher cellulose than RX in stem, or than CT in the whole plant. Furthermore, varieties AC, KG, VRU and TAI were resistant to lodging and had a higher fiber content, so they are recommended as energetic crops.