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Highlights: [•] Kinetics study on levoglucosan primary decomposition in cellulose pyrolysis. [•] Including C–O bond scission, C–C bond scission, and levoglucosan dehydration. [•] Transition state calculation without tunneling correction is suitable method. [•] Arrhenius equation for every elementary reaction and every pathway are obtained. [•] One dehydration pathway is a preferred pathway for levoglucosan decomposition. [ABSTRACT FROM AUTHOR]

Abstract: Steam explosion (SE) pretreatment is served to separate the main components of woody biomass. In general there is a noticeable gap in literature in terms of application of steam explosion process to upgrade biomass fuel for wood pellet production. In order to study the influence of steam explosion pretreatment on biomass fuel, Salix wood chips was used as raw material. Four different SE experiments were performed by varying two key process factors; time and temperature. Elementary quality and ash properties of the pretreated residue were investigated. Moreover, physical and thermochemical properties of the pellet, produced from the residue, were also investigated. Reduction in ash content especially in alkali metals was observed in steam treated residue. Pretreatment of biomass also enhanced carbon content and reduced oxygen amount in the fuel which enhanced the heating value of the fuel. Moreover, pretreatment enhanced pellet density, impact resistance, and abrasive resistance of pellet. However, small degradation in ash fusion characteristics and char reactivity was also observed as the severity of the process increased. [Copyright &y& Elsevier]

Abstract: The processing of agricultural crops results in waste, which is a potential energy resource for alleviating commercial energy supply problems to agricultural-led economies like Tanzania. The energy content of the individual agricultural waste is largely dependent on its chemical composition (C, H and O) and it is negatively affected by the inclusion of inorganic elements and moisture. In this work, fifteen tropical agricultural wastes emanating from export crops for Tanzania were analyzed. The methods used to analyze involved performing proximate and ultimate analysis for determining the biomass composition. Thermal degradation characteristic was established to five selected wastes (coffee husks, sisal bole, cashew nut shells, palm stem, and bagasse) using a thermogravimetric analyzer type NETZSCH STA 409 PC Luxx at a heating rate of 10K/min. On the basis of elemental composition, the palm fibre and cashew nut shells exhibited high energy content due to their higher H:C ratio with relatively low O:C ratio. Results of the thermal degradation characteristic study showed that the cashew nut shells were the most reactive feedstocks due to their highest overall mass loss and lowest burnout temperatures of 364°C. Further, kinetic studies done to the five tropical biomass feedstocks under the pseudo single-component overall model established the activation energy for the bagasse, palm stem, and cashew nut shells to be 460kJ/mole, 542kJ/mole, and 293kJ/mole, respectively. The respective activation energies for coffee husks and sisal bole were 370kJ/mole and 239kJ/mole. With the exception of the sisal bole, which exhibited zero order reaction mechanism, the remaining materials´ reaction mechanism was of first order. These experimental findings form a basis for ranking these materials for energy generation and provide necessary input to equipment and process designers. [ABSTRACT FROM AUTHOR]

In a biomass gasification process, condensation of inorganic species can cause problems such as corrosion and deposition on the downstream equipment. In this work, in order to investigate the condensation of inorganics during the gas cooling step of the biomass gasification system, both experimental and modelling studies were conducted. Experiments were performed on a pilot-scale steam/oxygen blown fluidized bed gasification facility. A CO 2 cooled probe was located at the head of a filter to condense inorganic species. Five thermocouples were used to monitor the probe temperature profile. Deposits on the probe were characterized using scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDS) to analyze the elemental composition of deposits. A process model based on the local chemical and phase equilibriums was developed using software SimuSage to predict both release and condensation of inorganics. A customized thermodynamic database extracted from the FactSage 7.1 was used during model calculations. Two cases including with and without addition of bed material were calculated. Results show that the identified elemental compositions of deposit under different gas cooling temperatures reasonably agree with the elemental compositions predicted by model calculations. This demonstrates that the established model and the customized thermodynamic data are valid. A large amount of carbon is identified in the deposit of low temperature probe sections, which may come from the condensed tar. Additionally, a temperature window is found, where melts are formed during gas cooling. [ABSTRACT FROM AUTHOR]

Highlights: [•] An equation was developed for pressure drop prediction with shrinking effect. [•] Graphical representations of correlation constants were introduced. [•] This would provide a guide to select pellet size and designing a grate. [ABSTRACT FROM AUTHOR]

Abstract: Torrefied biomass has several benefits, such as higher energy density, good grindability, higher flowability and uniformity. The process of torrefaction moves the chemical and physical properties of raw biomass close to that of bituminous coal, which allows co-utilization with high substitution ratios of biomass in the existing coal-fired boilers without major modifications. In this study, a torrefaction based co-firing system was proposed and studied. Devolatilization and char oxidize kinetics of the torrefied biomass have been investigated experimentally. CFD modeling of co-firing with varying substitutions of torrefied biomass in a pulverized coal boiler have been carried out. To figure out the boiler performance when co-firing torrefied biomass, five different cases were involved and simulated, coal only, 25% biomass, 50% biomass, 75% biomass, and 100% biomass on thermal basis, respectively. The results showed torrefaction is able to provide a technical option for high substitution ratios of biomass in the co-firing system. The case-study pulverized coal boiler could be fired 100% torrefied biomass without obvious decreasing of the boiler efficiency and fluctuation of boiler load. More positively, the net CO2 and the NO x emissions significantly reduced with increasing of biomass substitutions in the co-firing system. [Copyright &y& Elsevier]

The promising properties of torrefied biomass provide a valid co-firing option for large percentage biomass utilization in existing coal-fired boilers. Torrefied biomass is expected to have a better combustion stability than raw biomass and similar to that of coal. The present work will characterizes the oxidation properties of torrefied biomass char and compare with that of raw biomass char. The studied two chars are produced from raw and torrefied biomass in an Isothermal Plug Flow Reactor (IPFR) at high temperature and high heating rate, a sufficient residence time is applied for the completion of the high temperature devolatilization. Char oxidation tests are carried out in the IPFR by varying temperature, oxygen concentration and residence time. The reactivity of two studied chars are analyzed and compared with referenced biomass char and coal char, and the impact of torrefaction on char reactivity is also discussed in this paper. Finally, the char oxidation kinetic parameters are determined using a parameter optimization method, and the obtained kinetics are examined by comparing the experimental and predicted mass conversions. [ABSTRACT FROM AUTHOR]

Highlights: [•] The performances of torrefaction based co-firing power plant are simulated by using Aspen Plus. [•] Mass loss properties and released gaseous components have been studied during biomass torrefaction processes. [•] Mole fractions of CO2 and CO account for 69–91% and 4–27% in total torrefied gases. [•] The electrical efficiency reduced when increasing either torrefaction temperature or substitution ratio of biomass. [Copyright &y& Elsevier]

Pretreatment of biomass becomes more and more important due to the large scale application of biomass having low energy density. In this paper, steam exploded biomass pellets (Black pellets) and unpretreated biomass pellets (Gray pellets) were gasified with air and steam at an updraft HTAG (High Temperature Agent Gasification) unit. Decomposition characteristics of pellets were first analyzed with TGA (thermo gravimetric analysis). Early decomposition of hemicellulose and cellulose were seen with Black pellets around 241 °C and 367 °C respectively. Introducing CO2 led comparatively high mass loss rate with Black pellets. Gasification of Black pellets resulted in syngas with high CO and hydrocarbon contents while Gasification of Gray pellets resulted in high H2 content of syngas. LHV (lower heating value) of syngas was high around 7.3 MJ/Nm3 and 10.6 MJ/Nm3 with air gasification and steam gasification respectively. Even with significantly low syngas temperature with gasification of Black pellets, only slightly high total tar content was seen compared to that of Gray pellets gasification. Phenolic compounds dominated the tar composition. In general, steam gasification of Black pellets seems to be more feasible if syngas with high energy value is desired. If higher H2 yield is preferred, gasification of unpretreated pellets likely to be more attractive. [ABSTRACT FROM AUTHOR]

Abstract: Analyses made on the world''s biomass energy potential show that biomass energy is the most abundant sustainable renewable energy. The available technical biomass energy potential surpasses the total world''s consumption levels of petroleum oils, coal and natural gas. In order to achieve a sustainable harnessing of the biomass energy potential and to increase its contribution to the world''s primary energy consumption, there is therefore a need to develop and sustain contemporary technologies that increase the biomass-to-energy conversion. One such technology is the high temperature air/steam gasification (HTAG) of biomass. In this paper we present findings of gasification experimental studies that were conducted using coffee husks under high temperature conditions. The experiments were performed using a batch facility, which was maintained at three different gasification temperatures of 900°C, 800°C, and 700°C. The study findings exhibited the positive influence of high temperature on increasing the gasification process. Chars left while gasifying at 800°C and 700°C were respectively 1.5 and 2.4times that for the case of 900°C. Furthermore, increased gasification temperature led to a linear increment of CO concentration in the syngas for all gasification conditions. The effect was more pronounced for the generally poorly performing gasification conditions of N2 and 2% oxygen concentration. When gasification temperature was increased from 700°C to 900°C the CO yield for the 2% O2 concentration increased by 6times and that of N2 condition by 2.5times. The respective increment for the 3% and 4% O2 conditions were only twofold. This study estimated the kinetic parameters for the coffee husks thermal degradation that exhibited a reaction mechanism of zero order with apparent activation energy of 161kJ/mol and frequency factor of 3.89×104/min. [Copyright &y& Elsevier]

• Significant reduction of Alkali and Alkaline Earth Metal (AAEM) in the biomass with acid-leaching treatment. • The Higher Heating Value (HHV) is not significantly influenced by the acid-leaching treatment. • The removal of AAEM significantly affected the degradation of hemicellulose, cellulose, and lignin. • The second order (F2) mechanism can illustrate the catalytic pyrolysis process of lignocellulose biomass. • Acid-leaching process prior to catalytic pyrolysis promotes high devolatilization and reaction rate. Improvements on the pyrolysis process of biomass fuels are needed to obtain a high-quality of bio-oil. Pre-treatment by acid leaching prior to the pyrolysis process is considered to remove Alkali and Alkaline Earth Metal (AAEM) from the biomass, since AAEM adversely affect the catalytic pyrolysis process. Therefore, the main objective of the present work was to determine and compare the effect of mixed-catalysts consisting of H-ZSM-5 and Al-MCM-41, which are used at different ratios in lignocellulose biomass pyrolysis via Thermal Gravimetric Analysis (TGA) for both, un-leached and leached biomass. In addition, the activation energies have been determined based on the solid-state reaction mechanism. The results from the acid leaching treatment showed that the optimum leaching process was set to 30 min, 30 °C and 5 wt% acetic acid in the leaching liquid. This resulted in 59%, 95%, 99%, and 96% reduction degree of Calcium (Ca), Magnesium (Mg), Potassium or Kalium (K), and Natrium (Na), respectively. The Higher Heating Values (HHVs) for un-leached and leached biomass were 19.42 and 19.14 MJ/kg, respectively, calculated by using the Milne formula. The HHV value is not significantly influenced by the acid-leaching pre-treatment. Thermogravimetric analysis showed similar trends for the mass loss as a function of temperature and four stages could be determined from the thermal degradation of biomass. There was no significant shift in the temperature profiles between un-leached and leached biomass degradations. However, the removal of AAEM significantly affected the degradation of hemicellulose, cellulose, and lignin. A 12.4–18.2% increase of mass losses could be found in Phase 2 for leached biomass, compared to un-leached biomass. The mass losses in Phase 2 also increased with increased heating rates. From the un-leached biomass experiments using a catalyst mixture, the percentage of mass loss increased from 64.95 wt% at 10 K min−1 to 68.33 wt% at 50 K min−1. Moreover, for the leached biomass, it rose from 65.71 wt% at 10 K min−1 to 66.73 wt% at 30 K min−1, before decreasing to 62.44 wt% at 50 K min−1. A lower mass loss in Phase 4 for leached biomass compared to un-leached biomass showed the influence of an AAEM removal. The second order (F2) mechanism was able to illustrate the catalytic pyrolysis process, proven by the result that the coefficient of determination (R2) was higher than 0.99, which was high compared to other mechanisms. An acid leaching pre-treatment led to a reduction in the activation energies. The activation energies for the un-leached biomass were 26.94 and 25.56 kJ mol−1 at a heating rate of 10 K min−1 for a process without and with a catalyst mixture, respectively. The activation energies for leached biomass were 24.05 and 21.80 kJ mol−1. The results also showed that the use of the acid leaching process as a treatment prior to catalytic pyrolysis is positive, since it resulted in high devolatilization and reaction rate. [ABSTRACT FROM AUTHOR]