Torrefaction and co-torrefaction characterization of hemicellulose, cellulose and lignin as well as torrefaction of some basic constituents in biomass

Torrefaction is a thermal pretreatment process for biomass where raw biomass is heated in the temperatures of 200-300 °C under an inert or nitrogen atmosphere. The main constituents contained in biomass include hemicellulose, cellulose and lignin; therefore, the thermal decomposition characteristics of these constituents play a crucial role in determining the performance of torrefaction of lignocellulosic materials. To gain a fundamental insight into biomass torrefaction, five basic constituents, including hemicellulose, cellulose, lignin, xylan and dextran, were individually torrefied in a thermogravimetry. Two pure materials, xylose and glucose, were torrefied as well for comparison. Three torrefaction temperatures of 230, 260 and 290 °C, corresponding to light, mild and severe torrefactions, were taken into account. The experiments suggested the weight losses of the tested samples could be classified into three groups; they consisted of a weakly active reaction, a moderately active reaction and a strongly active reaction, depending on the natures of the tested materials. Co-torrefactions of the blend of hemicellulose, cellulose and lignin at the three torrefaction temperatures were also examined. The weight losses of the blend were very close to those from the linear superposition of the individual samples, suggesting that no synergistic effect from the co-torrefactions was exhibited.     

A study on torrefaction of various biomass materials and its impact on lignocellulosic structure simulated by a thermogravimetry

Torrefaction processes of four kinds of biomass materials, including bamboo, willow, coconut shell and wood (Ficus benjamina L.), were investigated using the thermogravimetric analysis (TGA). Particular emphasis is placed on the impact of torrefaction on hemicellulose, cellulose and lignin contained in the biomass. Two different torrefaction processes, consisting of a light torrefaction process at 240 °C and a severe torrefaction process at 275 °C, were considered. From the torrefaction processes, the biomass could be divided into two groups; one was the relatively active biomass such as bamboo and willow, and the other was the relatively inactive biomass composed of coconut shell and wood. When the light torrefaction was performed, the results indicated that the hemicellulose contained in the biomass was destroyed in a significant way, whereas cellulose and lignin were affected only slightly. Once the severe torrefaction was carried out, it further had a noticeable effect on cellulose, especially in the bamboo and willow. The light torrefaction and severe torrefaction were followed by a chemically frozen zone, regardless of what the biomass was. From the viewpoint of torrefaction application, the investigated biomass torrefied in less than 1 h with light torrefaction is an appropriate operation for producing fuels with higher energy density.     

An evaluation on improvement of pulverized biomass property for solid fuel through torrefaction

The improvement on physical and chemical properties of pulverized biomass from torrefaction is investigated to evaluate the potential of biomass as solid fuel used in boilers and blast furnaces. Three biomasses of bamboo, banyan and willow are considered. The results indicate that when the torrefaction temperature is relatively low such as 230 and 260 °C, the weight loss of biomass depends significantly on the temperature, as a result of consumptions of hemicellulose and cellulose. However, once the torrefaction temperature is as high as 290 °C, the weight losses of various biomass materials tend to become uniform. The decreased O/C ratio in biomass from torrefaction can be explained by intensified lignin content in that the O/C ratio in lignin is low compared to that in hemicellulose and cellulose. Furthermore, the enriched element C in torrefied biomass results in an increase in the calorific value of the torrefied materials. However, the enlarged higher heating value (HHV) of biomass from torrefaction cannot keep up with the weight loss; this leads to the decrease in total energy of biomass as the torrefaction temperature rises. The conducted correlation in predicting the HHV of raw biomass can also be utilized for torrefied biomass. The raw pulverized biomasses are characterized by agglomeration in the regime of smaller particle size. Once the biomasses undergo torrefaction, the dispersion of powder is improved, thereby facilitating the injection of biomass powder. This enhances the applications of pulverized biomass in boilers and blast furnaces.     

Comparative study on pyrolysis and catalytic pyrolysis upgrading of biomass model compounds: Thermochemical behaviors,kinetics, and aromatic hydrocarbon formation

In order to understand the pyrolysis mechanism, reaction kinetic and product properties of biomass and select suitable agricultural and forestry residues for the generation desired products, the pyrolysis and catalytic pyrolysis characteristics of three main components (hemicellulose, cellulose, and lignin) of biomass were investigated using a thermogravimetric analyzer (TGA) with a fixed-bed reactor. Fourier transform infrared spectroscopy (FTIR) and elemental analysis were used for further characterization. The results showed that: the thermal stability of hemicellulose was the worst, while that of cellulose was higher with a narrow range of pyrolysis temperatures. Lignin decomposed over a wider range of temperatures and generated a higher char yield. After catalytic pyrolysis over HZSM-5 catalyst, the conversion ratio increased. The ratio for the three components was in the following order: lignincellulose < biomass < xylan. The Starink method was introduced to analyze the thermal reaction kinetics, activation energy (Ea), and the pre-exponential factor (A). The addition of HZSM-5 improved the reactivity and decreased the activation energy in the following order: xylan (30.54%) > biomass(15.41%) > lignin (14.75%) > cellulose (6.73%). The pyrolysis of cellulose gave the highest yield of bio-oil rich in levoglucosan and other anhydrosugars with minimal coke formation. Xylan gave a high gas yield and moderate yield of bio-oil rich in furfural, while lignin gave the highest solid residue and produced the lowest yield of bio-oil that was rich in phenolic compounds. After catalytic pyrolysis, xylan gave the highest yield of monocyclic aromatic hydrocarbons, 76.40%, and showed selectivity for benzene and toluene. Cellulose showed higher selectivity for xylene and naphthalene; however, lignin showed enhanced for selectivity of C10 + polycyclic aromatic hydrocarbons. Thus, catalytic pyrolysis method can effectively improve the properties of bio-oil and bio-char.     

Biomass upgrading by torrefaction for the production of biofuels: A review

An overview of the research on biomass upgrading by torrefaction for the production of biofuels is presented. Torrefaction is a thermal conversion method of biomass in the low temperature range of 200–300 °C. Biomass is pre-treated to produce a high quality solid biofuel that can be used for combustion and gasification. In this review the characteristics of torrefaction are described and a short history of torrefaction is given. Torrefaction is based on the removal of oxygen from biomass which aims to produce a fuel with increased energy density by decomposing the reactive hemicellulose fraction. Different reaction conditions (temperature, inert gas, reaction time) and biomass resources lead to various solid, liquid and gaseous products. A short overview of the different mass and energy balances is presented. Finally, the technology options and the most promising torrefaction applications and their economic potential are described.     

TGA and kinetic study of different torrefaction conditions of wood biomass under air and oxy-fuel combustion atmospheres

Combustion and oxy-fuel combustion characteristics of torrefied pine wood chips were investigated by Thermogravimetric Analysis (TGA). Three torrefaction temperatures (250, 300, and 350 °C) and two residence times (15 and 30 min) were considered. Experiments were carried out at three heating rates of 10, 20, and 40 °C/min. The isoconversional kinetic methods of FWO, KAS, and Friedman were employed to estimate the activation energies. The assessment of uncertainty in obtaining the activation energy values was also considered. The obtained results indicated that due to torrefaction, the O/C and H/C atomic ratios decreased, resulting the 300ºC-30 min and 350ºC-15 min torrefied biomass to be completely embedded in lignite region in van-Krevelen's diagram. Oxy-fuel combustion affected the decomposition of cellulose and lignin components of biomass while the impact on the hemicellulose component was negligible. The kinetic analysis revealed that with the evolution of conversion degree, the activation energy values increased during hemicellulose degradation, remained approximately constant during cellulose decomposition and showed a sharp decrease for lignin decomposition. The activation energy trends were comparable in both air and oxy-fuel combustion conditions, however slight changes in activation energy values were noticed. The highest activation energy value was obtained for 250ºC-30 min torrefied biomass at 183.40 kJ/mol and the lowest value was 72.93 kJ/mol for 350ºC-15 min biomass. The uncertainty values related to FWO method were lower than KAS and Friedman methods. The uncertainty values for FWO and KAS methods were at the range of 5–15%.     

Experimental study on the ignition characteristics of cellulose,hemicellulose, lignin and their mixtures

Ignition behaviour of biomass is an essential knowledge for plant design and process control of biomass combustion. Understanding of ignition characteristics of its main chemical components, i.e. cellulose, hemicellulose, lignin and their mixtures will allow the further investigation of ignition behaviour of a wider range of biomass feedstock. This paper experimentally investigates the influences of interactions among cellulose, hemicellulose and lignin on the ignition behaviour of biomass by thermogravimetric analysis. Thermal properties of an artificial biomass, consisting of a mixture of the three components will be studied and compared to that of natural biomass in atmospheres of air and nitrogen in terms of their ignition behaviour. The results showed that the identified ignition temperatures of cellulose, hemicellulose and lignin are 410 °C, 370 °C and 405 °C, respectively. It has been found that the influence of their interactions on the ignition behaviour of mixtures is insignificant, indicating that the ignition behaviour of various biomass feedstock could be predicted with high accuracy if the mass fractions of cellulose, hemicellulose and lignin are known. While the deficiencies of the determined mutual interactions would be further improved by the analytical results of the activation energies of cellulose, hemicellulose, lignin, their mixtures as well as natural and artificial biomass in air conditions.     

Effects of torrefaction on the physiochemical properties of oil palm empty fruit bunches,mesocarp fiber and kernel shell

In this work, the effects of torrefaction on the physiochemical properties of empty fruit bunches (EFB), palm mesocarp fiber (PMF) and palm kernel shell (PKS) are investigated. The change of properties of these biomass residues such as CHNS mass fraction, gross calorific value (GCV), mass and energy yields and surface structure when subjected to torrefaction process are studied. In this work, these materials with particle size in the range of 355–500 μm are torrefied under light torrefaction conditions (200, 220 and 240 °C) and severe torrefaction conditions (260, 280 and 300 °C). TGA is used to monitor the mass loss during torrefaction while tube furnace is used to produce significant amount of products for chemical analyses. In general, the study reveals torrefaction process of palm oil biomass can be divided into two main stages through the observation on the mass loss distribution. The first stage is the dehydration process at the temperature below than 105 °C where the mass loss is in the range of 3–5%. In the second stage, the decomposition reaction takes place at temperature of 200–300 °C. Furthermore, the study reveals that carbon mass fraction and gross calorific value (GCV) increase with the increase of torrefaction temperature but the O/C ratio, hydrogen and oxygen mass fractions decrease for all biomass. Among the biomass, torrefied PKS has the highest carbon mass fraction of 55.6% when torrefied at 300 °C while PMF has the highest GCV of 23.73 MJ kg⁻¹ when torrefied at the same temperature. Both EFB and PMF produce lower mass fraction than PKS when subjected to same torrefaction temperature. In terms of energy yield, PKS produces 86–92% yield when torrefied at light to severe torrefaction conditions, until 280 °C. However, both EFB and PMF only produce 70–78% yield at light torrefaction conditions, until 240 °C. Overall, the mass loss of 45–55% of these biomasses is observed when subjected to torrefaction process. Moreover, SEM images reveal that torrefaction has more severe impact on surface structure of EFB and PMF than that of PKS especially under severe torrefaction conditions. The study concludes that the torrefaction process of these biomass has to be optimized based on the type of the biomass in order to offset the mass loss of these materials through the process and increase the energy value of the solid product.     

Optimisation of dilute alkaline pretreatment for enzymatic saccharification of wheat straw

Physico-chemical pretreatment of lignocellulosic biomass is critical in removing substrate-specific barriers to cellulolytic enzyme attack. Alkaline pretreatment successfully delignifies biomass by disrupting the ester bonds cross-linking lignin and xylan, resulting in cellulose and hemicellulose enriched fractions. Here we report the use of dilute alkaline (NaOH) pretreatment followed by enzyme saccharifications of wheat straw to produce fermentable sugars. Specifically, we have assessed the impacts of varying pretreatment parameters (temperature, time and alkalinity) on enzymatic digestion of residual solid materials. Following pretreatment, recoverable solids and lignin contents were found to be inversely proportional to the severity of the pretreatment process. Elevating temperature and alkaline strengths maximised hemicellulose and lignin solubilisation and enhanced enzymatic saccharifications. Pretreating wheat straw with 2% NaOH for 30 min at 121 °C improved enzyme saccharification 6.3-fold when compared to control samples. Similarly, a 4.9-fold increase in total sugar yields from samples treated with 2% NaOH at 60 °C for 90min, confirmed the importance of alkali inclusion. A combination of three commercial enzyme preparations (cellulase, ??-glucosidase and xylanase) was found to maximise monomeric sugar release, particularly for substrates with higher xylan contents. In essence, the combined enzyme activities increased total sugar release 1.65-fold and effectively reduced cellulase enzyme loadings 3-fold. Prehydrolysate liquors contained 4-fold more total phenolics compared to enzyme saccharification mixtures. Harsher pretreatment conditions provide saccharified hydrolysates with reduced phenolic content and greater fermentation potential.     

Engineered pellets from dry torrefied and HTC biochar blends

Dry torrefaction and hydrothermal carbonization (HTC) are two thermal pretreatment processes for making homogenized, carbon rich, hydrophobic, and energy dense solid fuel from lignocellulosic biomass. Pellets made from torrefied biochar have poor durability compared to pellets of raw biomass. Durability, mass density, and energy density of torrefied biochar pellets decrease with increasing dry torrefaction temperature. Durable pellets of torrefied biochar may be engineered for high durability using HTC biochar as a binder. In this study, biomass dry torrefied for 1 h at 250, 275, 300, and 350 °C was pelletized with various proportions of biomass HTC treated at 260 °C for 5 min. During the pelletization of biochar blends, HTC biochar fills the void spaces and makes solid bridges between torrefied biochar particles, thus increasing the durability of the blended pellets. The engineered pellets' durability is increased with increasing HTC biochar fraction. For instance, engineered pellets of 90% Dry 300 and 10% HTC 260 are 82.5% durable, which is 33% more durable than 100% Dry 300 biochar pellets, and also have 7% higher energy density than 100% Dry 300 biochar pellets.     

Thermal behavior of lignocellulosic materials under aerobic/anaerobic environments

Utilization of lignocellulosic material via thermo-chemical processes has received huge attention from both biofuel and biochemical sectors. Intensive research has been embarked to study the thermal behavior and the decomposition patterns of the potential feedstock materials. Palm plantation waste, empty palm fruit's bunches (EFB) are used as a biomass source in this experiment. A comparison study was made using basic lignocellulosic model compounds such as hemicellulose, cellulose, and lignin. The thermal stability of each compound in both oxygen and nitrogen environments was investigated. The degradation of model compounds were categorized into primary (200–400 °C) and secondary (500–800 °C) stages based on structural collapse and liquid/solid decompositions. Besides, the influence of inorganic substances in EFB degradation was reported whereby the mineral contents act as a catalyst by enhancing the decomposition at lower temperatures compared to demineralized EFB. In addition, the product gas evolutions from the gasification reaction of the components were analyzed using online mass spectrometer. The gas production patterns indicate the nature of the compounds in terms of thermal stability, functional group cleavages and catalytic reactions.     

Pyrolysis-catalytic steam reforming of agricultural biomass wastes and biomass components for production of hydrogen/syngas

The pyrolysis-catalytic steam reforming of six agricultural biomass waste samples as well as the three main components of biomass was investigated in a two stage fixed bed reactor. Pyrolysis of the biomass took place in the first stage followed by catalytic steam reforming of the evolved pyrolysis gases in the second stage catalytic reactor. The waste biomass samples were, rice husk, coconut shell, sugarcane bagasse, palm kernel shell, cotton stalk and wheat straw and the biomass components were, cellulose, hemicellulose (xylan) and lignin. The catalyst used for steam reforming was a 10 wt.% nickel-based alumina catalyst (NiAl₂O₃). In addition, the thermal decomposition characteristics of the biomass wastes and biomass components were also determined using thermogravimetric analysis (TGA). The TGA results showed distinct peaks for the individual biomass components, which were also evident in the biomass waste samples reflecting the existence of the main biomass components in the biomass wastes. The results for the two-stage pyrolysis-catalytic steam reforming showed that introduction of steam and catalyst into the pyrolysis-catalytic steam reforming process significantly increased gas yield and syngas production notably hydrogen. For instance, hydrogen composition increased from 6.62 to 25.35 mmol g^?1 by introducing steam and catalyst into the pyrolysis-catalytic steam reforming of palm kernel shell. Lignin produced the most hydrogen compared to cellulose and hemicellulose at 25.25 mmol g^?1. The highest residual char production was observed with lignin which produced about 45 wt.% char, more than twice that of cellulose and hemicellulose.     

Optimization and modeling of process parameters during hydrothermal gasification of biomass model compounds to generate hydrogen-rich gas products

Hydrothermal gasification in subcritical and supercritical water is gaining attention as an attractive option to produce hydrogen from lignocellulosic biomass. However, for process optimization, it is important to understand the fundamental phenomenon involved in hydrothermal gasification of synthetic biomass or biomass model compounds, namely cellulose, hemicellulose and lignin. In this study, the response surface methodology using the Box-Behnken design was applied for the first time to optimize the process parameters during hydrothermal (subcritical and supercritical water) gasification of cellulose. The process parameters investigated include temperature (300–500 °C), reaction time (30–60 min) and feedstock concentration (10–30 wt%). Temperature was found to be the most significant factor that influenced the yields of hydrogen and total gases. Furthermore, negligible interaction was found between lower temperatures and reaction time while the interaction became dominant at higher temperatures. Hydrogen yield remained at about 0.8 mmol/g with an increase in the reaction time from 30 min to 60 min at the temperature range of 300–400 °C. When the temperature was raised to 500 °C, hydrogen yield started to elevate at longer reaction time. Maximum hydrogen yield of 1.95 mmol/g was obtained from supercritical water gasification of cellulose alone at 500 °C with 12.5 wt% feedstock concentration in 60 min. Using these optimal reaction conditions, a comparative evaluation of the gas yields and product distribution of cellulose, hemicellulose (xylose) and lignin was performed. Among the three model compounds, hydrogen yields increased in the order of lignin (0.73 mmol/g) < cellulose (1.95 mmol/g) < xylose (2.26 mmol/g). Based on the gas yields from these model compounds, a possible reaction pathway of model lignocellulosic biomass decomposition in supercritical water was proposed.     

Comparative studies on the pyrolysis of cellulose,hemicellulose, and lignin based on combined kinetics

The thermal degradation behavior and pyrolytic mechanism of cellulose, hemicellulose, and lignin are investigated at different heating rates from 10 Kmin^?1 to 100 Kmin^?1 with a step-size of 10 Kmin^?1 using thermogravimetric analysis (TGA) equipment. It is observed that there are one, two, and three stages of pyrolytic reactions takes place in cellulose, hemicellulose, and lignin respectively. Isoconversional method is not suitable to analyse pyrolysis of hemicellulose and lignin as it involves multi-step reactions. The activation energies of the main decomposition stage for cellulose, hemicellulose, and lignin are 199.66, 95.39, and 174.40 kJ mol^?1 respectively. It is deduced that the pyrolysis reaction of cellulose corresponds to random scission mechanism while the pyrolysis reaction of hemicellulose and lignin follows the order based reaction mechanisms.     

Supercritical water gasification of biomass for hydrogen production

Hydrogen from waste biomass is considered to be a clean gaseous fuel and efficient for heat and power generation due to its high energy content. Supercritical water gasification is found promising in hydrogen production by avoiding biomass drying and allowing maximum conversion. Waste biomass contains cellulose, hemicellulose and lignin; hence it is essential to understand their degradation mechanisms to engineer hydrogen production in high-pressure systems. Process conditions higher than 374 °C and 22.1 MPa are required for biomass conversion to gases. Reaction temperature, pressure, feed concentration, residence time and catalyst have prominent roles in gasification. This review focuses on the degradation routes of biomass model compounds such as cellulose and lignin at near and supercritical conditions. Some homogenous and heterogeneous catalysts leading to water–gas shift, methanation and other sub-reactions during supercritical water gasification are highlighted. The parametric impacts along with some reactor configurations for maximum hydrogen production and technical challenges encountered during hydrothermal gasification processes are also discussed.     

Pretreatment and fractionation of barley straw using steam explosion at low severity factor

Agricultural residues represent an abundant, readily available, and inexpensive source of renewable lignocellulosic biomass. However, biomass has complex structural formation that binds cellulose and hemicellulose. This necessitates the initial breakdown of the lignocellulosic matrix. Steam explosion pretreatment was performed on barley straw grind to assist in the deconstruction and disaggregation of the matrix, so as to have access to the cellulose and hemicellulose. The following process and material variables were used: temperature (140–180 °C), corresponding saturated pressure (500–1100 kPa), retention time (5–10 min), and mass fraction of water 8–50%. The effect of the pretreatment was assessed through chemical composition analysis. The severity factor R_o, which combines the temperature and time of the hydrolytic process into a single reaction ordinate was determined. To further provide detailed chemical composition of the steam exploded and non-treated biomass, ultimate analysis was performed to quantify the elemental components. Data show that steam explosion resulted in the breakdown of biomass matrix with increase in acid soluble lignin. However, there was a considerable thermal degradation of cellulose and hemicellulose with increase in acid insoluble lignin content. The high degradation of the hemicellulose can be accounted for by its amorphous nature which is easily disrupted by external influences unlike the well-arranged crystalline cellulose. The carbon content of the solid steam exploded product increased at higher temperature and longer residence time, while the hydrogen and oxygen content decreased, and the higher heating value (HHV) increased.     

Influence of mineral matter on pyrolysis of palm oil wastes

The influence of mineral matter on pyrolysis of biomass (including pure biomass components, synthesized biomass, and natural biomass) was investigated using a thermogravimetric analyzer (TGA). First, the mineral matter, KCl, K₂CO₃, Na₂CO₃, CaMg(CO₃)₂, Fe₂O₃, and Al₂O₃, was mixed respectively with the three main biomass components (hemicellulose, cellulose, and lignin) at a weight ratio (C/W) of 0.1 and its pyrolysis characteristics were investigated. Most of these mineral additives, except for K₂CO₃, demonstrated negligible influence. Adding K₂CO₃ inhibited the pyrolysis of hemicellulose by lowering its mass loss rate by 0.3 wt%/°C, while it enhanced the pyrolysis of cellulose by shifting the pyrolysis to a lower temperature. With increased K₂CO₃ added, the weight loss of cellulose in the lower temperature zone (200-315 °C) increased greatly and the activation energies of hemicellulose and cellulose pyrolysis decreased notably from 204 to 42 kJ/mol. Second, studies on the synthetic biomass of hemicellulose, cellulose, lignin, and K₂CO₃ (as a representative of minerals) indicated that peaks of cellulose and hemicellulose pyrolysis became overlapped with addition of K₂CO₃ (at C/W = 0.05-0.1), due to the catalytic effect of K₂CO₃ lowering cellulose pyrolysis to a lower temperature. Finally, a local representative biomass—palm oil waste (in the forms of original material and material pretreated through water washing or K₂CO₃ addition)—was studied. Water washing shifted pyrolysis of palm oil waste to a higher temperature by 20 °C, while K₂CO₃ addition lowered the peak temperature of pyrolysis by . It was therefore concluded that the obvious catalytic effect of adding K₂CO₃ might be attributed to certain fundamental changes in terms of chemical structure of hemicellulose or decomposition steps of cellulose in the course of pyrolysis.     

Compositional differences among upland and lowland switchgrass ecotypes grown as a bioenergy feedstock crop

Feedstock quality mainly depends upon the biomass composition and bioenergy conversion system being used. Higher cellulose and hemicellulose concentrations are desirable for biochemical conversion, whereas higher lignin is favored for thermochemical conversion. The efficiency of these conversion systems is influenced by the presence of high nitrogen and ash concentrations. Switchgrass (Panicum virgatum L.) varieties are classified into two ecotypes based on their habitat preferences, i.e., upland and lowland. The objectives of this study were to quantify the chemical composition of switchgrass varieties as influenced by harvest management, and to determine if ecotypic differences exist among them. A field study was conducted near Ames, IA during 2012 and 2013. Upland (‘Cave-in-Rock’, ‘Trailblazer’ and ‘Blackwell’) and lowland switchgrass varieties (‘Kanlow’ and ‘Alamo’) were grown in a randomized block design with six replications. Six biomass harvests were collected at approximately 2-week intervals each year. In both years, delaying harvest increased cellulose, hemicellulose and lignin concentrations while decreasing nitrogen and ash concentrations in all varieties. On average, Kanlow had the highest cellulose and hemicellulose concentration (354 and 321 g kg⁻¹ DM respectively), and Cave-in-Rock had the highest lignin concentration (33 g kg⁻¹ DM). The lowest nitrogen and ash concentrations were observed in Kanlow (14 and 95 g kg⁻¹ DM respectively). In general, our results indicate that delaying harvest until fall improves feedstock quality, and ecotypic differences do exist between varieties for important feedstock quality traits. These findings also demonstrate potential for developing improved switchgrass cultivars as bioenergy feedstock by intermating lowland and upland ecotypes.     

Gasification efficiencies of cellulose,hemicellulose and lignin fractions of biomass in aqueous media by using Pt on activated carbon catalyst

The diversity in the chemical composition of lignocellulosic feedstocks can affect the conversion technologies employed for biofuel production. Aqueous-phase reforming (APR) activities of cellulose, hemicellulose and lignin components of lignocellulosic biomass materials were evaluated for production of hydrogen content gas mixture using platinum catalyst on activated carbon support. Wheat straw, an abundant by-product from wheat production and kenaf (Hibiscus cannabinus L.), an annual herbaceous plant growing very fast with low lodging susceptibility were used as lignocellulosics in the present study. The hydrolysates of cellulose fractions of biomass materials showed the best performance for gasification. The results indicated that hemicellulose isolated from kenaf was more sensitive to degradation and therefore, produced more gaseous products than that of wheat straw. The hemicellulose isolated from kenaf biomass left the lowest amount of ungasified solid residue in APR among other cellulose and hemicellulose materials studied. Lignin fractions of both biomass materials were not reactive in APR to produce hydrogen rich gas mixture.Gasification efficiencies of kenaf and wheat straw's hemicelluloses were also compared with xylans from beechwood and oat spelts which were commercially available as hemicellulosic fractions.Oat spelts xylan showed better reforming activity over the beechwood xylan.     

Characterisation of the torrefaction of beech wood using NIRS: Combined effects of temperature and duration

A new approach is proposed to retrace the combined effects of temperature and duration within the thickness of heat-treated Fagus sylvatica wood. Torrefaction is a mild pre-treatment of biomass carried out at 200-300 °C to improve its properties for pulverized systems such as gasification. The properties of wood treated at high temperature are closely related to chemical modifications induced by temperature levels and treatment duration. This study involved the spectral analysis of solid wood in the near infrared range with the aim of developing a predictive model for process assessment. Samples of beech wood were used for calibration under high temperature conditions of 220, 250 and 280 °C for 1 and 8 h. For prediction, a 50-mm thick solid piece of wood was treated at 250 °C for 3 h. It was demonstrated that it is possible not only to distinguish between wood samples that have undergone different heat treatments, but also to retrace the thermal history of a piece of wood. Statistical processing showed the compensatory effects of temperature and duration, along with the existence of an exothermal reaction in the solid piece of wood. It should thus be possible to ensure cheaper and faster quality control in continuous torrefaction processes.