Search

Recycling phosphorus from waste streams for fertilization purposes could contribute to a sustainable society. The production in the pulp and paper industry results in several waste streams, among others nutrient-rich sludges in different forms. This study presents a detailed chemical and 3D characterization of ash from co-combustion of bark and two types of sludges from a paper mill; mixed sludge and biosludge. The combustion performance was investigated for these experiments and advanced analysis methods were used to characterise the ashes to correlate chemical and physical properties relevant for nutrient recycling. The elemental composition was determined by energy-dispersive X-ray spectroscopy; dominating crystalline phases by X-ray diffraction; and morphology, porosity, pore size distribution and active surface area of the slag were analysed with synchrotron-based X-ray micro-tomography and image analysis. Slag was formed in all combustion experiments to a large extent with increasing amounts with a higher proportion of sludge. Nutrient amounts indicate that slag particles from co-combustion of both biosludge and mixed sludge can be useful either as a soil improvement directly or for recovery processes. Slag from combustion of 30 wt% biosludge and 70 wt% bark contained the highest amount of phosphorus, 9 at% on a C and O free basis. Evaluation of tomography data showed that discrete and open pores could be distinguished on a micrometre scale. The porosity of the slag varied between the replicates and fuel mixtures, on average between 17 and 23 vol% for the bark and sludge mixtures. Open pore volume displayed large variations, on average 39-56 vol% of the pores were open pores connected to the surrounding volume. For all samples, 90 % of the pores were small, with an equivalent diameter under 30 mu m, but the largest pore volume (80-90 %) consists of pores with an equivalent diameter over 75 mu m. In soils, pores with a minimum equivalent diameter over 30 mu m generally transmit water and the smaller pores store water. The slag particles have rela-tively thick walls, with few pore openings to the surroundings, indicating that the slag needs to be pre-treated by milling or crushing before application in the soil.

Combustion of phosphorus-rich residual streams can produce nutrient-rich ashes and these can be used either in further processing or as materials for direct nutrient recycling. The latter requires knowledge on morphological parameters of such ash particles that may impact plant growth, nutrient availability, and soil physical properties. The present work aims to determine the porosity, pore size, and specific surface area of ash particles, and discuss these properties in light of literature concerning interaction with soil water and plant roots. Bottom ash particles from combustion of sewage sludge and wheat straw and their co-combustion were analysed with X-ray microtomography. Image analysis provided information on morphology, specific surface area, porosity, and pore structure on a micrometre scale resolution. Co-combusting sewage sludge with wheat straw resulted in differences in ash particles' porosity and pore structure compared to combustion of pure fuels. Pure wheat straw ash displayed 62 vol% porosity while there was no apparent difference between 10 wt% or 30 wt% mixtures of sewage sludge, with a porosity of 29–31 vol%. Open pore volume comprise the largest part of the porosity (72–99 vol%) enabling interaction between surrounding pore water and nutrients. Overall, the ash particles display large open volume fractions and thin particle walls which may lead to rapid weathering and extensive interaction with soil water. The particles generally contained pore openings over 200 µm towards the surroundings, which provide opportunities for interaction with microbes and roots from a variety of plant species in addition to nutrient transport by soil water.

The effect of mechanical screening of severely contaminated forest fuel chips was investigated, focusing on main ash-forming elements and slagging tendency and other properties with relevance for thermal conversion. In this study, screening operations were performed according to practice on an industrial scale by combining a star screen and a supplementary windshifter in six different settings and combinations. Mechanical screening reduced the amount of ash and fine particles in the accept fraction. However, the mass losses for the different screening operations were substantial (20-50 wt %). Fuel analyses of the non-screened and the screened fuels showed that the most significant screening effect was a reduction of Si and Al, indicating an effective removal of sand and soil contaminations. However, the tested fuel's main ash-forming element's relative concentration did not indicate any improved combustion characteristics and ash-melting behavior. Samples of the accept fractions and non-screened material were combusted in a single-pellet thermogravimetric reactor, and the resulting ashes' morphology and elemental composition were analyzed by scanning electron microscopy-energy dispersive X-ray spectrometry and the crystalline phases by powder X-ray diffraction. Results from both these analyses confirmed that screening operations had no, or minor, effects on the fuels' ash chemistry and slagging tendencies, i.e., the fuels' proneness to ash melting was not improved. However, the reduction of ash and fine particles can reduce slagging and other operational problems in smaller and more sensitive combustion units.

This study compared the effects of hot-air pasteurisation (HAP) at 75–100 °C versus autoclaving at 121 °C and 2 bar overpressure on the lignocellulosic degradation process of birch-based substrates ...

A biomass amino silica-functionalized material was successfully prepared by a simple sol–gel method. 3-Aminopropyltriethoxysilane (APTES) was added to a tannin-rich grape residue to improve its physicochemical properties and enhance the adsorption performance. The APTES functionalization led to significant changes in the material’s characteristics. The functionalized material was efficiently applied in the removal of methyl orange (MO) due to its unique characteristics, such as an abundance of functional groups on its surface. The adsorption process suggests that the electrostatic interactions were the main acting mechanism of the MO dye removal, although other interactions can also take place. The functionalized biomass achieved a very high MO dye maximum adsorption capacity (Qmax) of 361.8 mg g–1. The temperature positively affected the MO removal, and the thermodynamic studies indicated that the adsorption of MO onto APTES-functionalized biomass was spontaneous and endothermic, and enthalpy is driven in the physisorption mode. The regeneration performance revealed that the APTES-functionalized biomass material could be easily recycled and reused by maintaining very good performance even after five cycles. The adsorbent material was also employed to treat two simulated dye house effluents, which showed 48% removal. At last, the APTES biomass-based material may find significant applications as a multifunctional adsorbent and can be used further to separate pollutants from wastewater.

The quality of wood powders depends on the size reduction technology used to produce them. The pre-drying, chipping, and conventional (impact and attritional) size reduction steps, commonly employed in industry, act to degrade wood and diminish its full potential as a renewable feedstock. In this study, the effect of using a new green (i.e. freshly harvested) milling technology, the multi-blade shaft mill (MBSM), on wood powder properties was investigated. Particle size distribution (PSD) and shape properties were measured by two-dimensional image analysis and surface area analysis was performed. The results showed that the MBSM can produce much finer powders compared to hammer milling, with particles demonstrating unique morphology and high specific surface area. Green wood milling yielded particles with the highest sphericity (0.64), aspect ratio (0.58), and micropore diameter (4.5 nm). Finer particles with spherical shapes enhanced the bulk density. Moreover, mill settings permit tailor-made powders according to the desired PSD.

The present work elucidates facile one-pot synthesis from biomass forestry waste (Norway spruce bark) and its chemical activation yielding high specific surface area (SBET) biochars as efficient lithium- and sodium-ion storage anodes. The chemically activated biochar using ZnCl2 (Biochar-1) produced a highly mesoporous carbon containing 96.1% mesopores in its structure as compared to only 56.1% mesoporosity from KOH-activated biochars (Biochar-2). The latter exhibited a lower degree of graphitization with disordered and defective carbon structures, while the former presented more formation of ordered graphite sheets in its structure as analyzed from Raman spectra. In addition, both biochars presented a high degree of functionalities on their surfaces but Biochar-1 presented a pyridinic-nitrogen group, which helps improve its electrochemical response. When tested electrochemically, Biochar-1 showed an excellent rate capability and the longest capacity retentions of 370 mA h g–1 at 100 mA g–1 (100 cycles), 332.4 mA h g–1 at 500 mA g–1 (1000 cycles), and 319 mA h g–1 at 1000 mA g–1 after 5000 cycles, rendering as an alternative biomass anode for lithium-ion batteries (LIBs). Moreover, as a negative electrode in sodium-ion batteries, Biochar-1 delivered discharge capacities of 147.7 mA h g–1 at 50 mA g–1 (140 cycles) and 126 mA h g–1 at 100 mA g–1 after 440 cycles. peerReviewed

This study utilized pulp and paper mill sludge as a carbon source to produce activated biochar adsorbents. The response surface methodology (RSM) application for predicting and optimizing the activated biochar preparation conditions was investigated. Biochars were prepared based on a Box–Behnken design (BBD) approach with three independent factors (i.e., pyrolysis temperature, holding time, and KOH:biomass ratio), and the responses evaluated were specific surface area (SSA), micropore area (Smicro), and mesopore area (Smeso). According to the RSM and BBD analysis, a pyrolysis temperature of 800 °C for 3 h of holding and an impregnation ratio of 1:1 (biomass:KOH) are the optimum conditions for obtaining the highest SSA (885 m2 g–1). Maximized Smicro was reached at 800 °C, 1 h and the ratio of 1:1, and for maximizing Smeso (569.16 m2 g–1), 800 °C, 2 h and ratio 1:1.5 (445–473 m2 g–1) were employed. The biochars presented different micro- and mesoporosity characteristics depending on pyrolysis conditions. Elemental analysis showed that biochars exhibited high carbon and oxygen content. Raman analysis indicated that all biochars had disordered carbon structures with structural defects, which can boost their properties, e.g., by improving their adsorption performances. The hydrophobicity–hydrophilicity experiments showed very hydrophobic biochar surfaces. The biochars were used as adsorbents for diclofenac and amoxicillin. They presented very high adsorption performances, which could be explained by the pore filling, hydrophobic surface, and π–π electron–donor–acceptor interactions between aromatic rings of both adsorbent and adsorbate. The biochar with the highest surface area (and highest uptake performance) was subjected to regeneration tests, showing that it can be reused multiple times. peerReviewed

In this work, Norway spruce (Picea abies(Karst) L.) bark was employed as a precursor to prepare activated carbon using zinc chloride (ZnCl2) as a chemical activator. The purpose of this study was to determine optimal activated carbon (AC) preparation variables by the response surface methodology using a Box–Behnken design (BBD) to obtain AC with high specific surface area (SBET), mesopore surface area (SMESO), and micropore surface area (SMICR). Variables and levels used in the design were pyrolysis temperature (700, 800, and 900 °C), holding time (1, 2, and 3 h), and bark/ZnCl2impregnation ratio (1, 1.5, and 2). The optimal conditions for achieving the highest SBETwere as follows: a pyrolysis temperature of 700 °C, a holding time of 1 h, and a spruce bark/ZnCl2ratio of 1.5, which yielded an SBETvalue of 1374 m2 g−1. For maximised mesopore area, the optimal condition was at a pyrolysis temperature of 700 °C, a holding time of 2 h, and a bark/ZnCl2ratio of 2, which yielded a SMESOarea of 1311 m2 g−1, where mesopores (SMESO%) comprised 97.4% of total SBET. Correspondingly, for micropore formation, the highest micropore area was found at a pyrolysis temperature of 800 °C, a holding time of 3 h, and a bark/ZnCl2ratio of 2, corresponding to 1117 m2 g−1, with 94.3% of the total SBETconsisting of micropores (SMICRO%). The bark/ZnCl2ratio and pyrolysis temperature had the strongest impact on the SBET, while the interaction between temperature and bark/ZnCl2ratio was the most significant factor for SMESO. For the SMICRO, holding time was the most important factor. In general, the spruce bark AC showed predominantly mesoporous structures. All activated carbons had high carbon and low ash contents. Chemical characterisation indicated that the ACs presented disordered carbon structures with oxygen functional groups on the ACs’ surfaces. Well-developed porosity and a large surface area combined with favourable chemical composition render the activated carbons from Norway spruce bark with interesting physicochemical properties. The ACs were successfully tested to adsorb sodium diclofenac from aqueous solutions showing to be attractive products to use as adsorbents to tackle polluted waters.Graphical abstract

Characterization of ash-generating elements is of great importance in bio-based processes using lignocellulosic biomass as feedstock. Spectral data using energy dispersive X-ray fluorescence (ED-XR ...

Biobased carbon materials (BBC) obtained from Norway spruce (Picea abies Karst.) bark was produced by single-step chemical activation with ZnCl2 or KOH, and pyrolysis at 800 °C for one hour. The chemical activation reagent had a significant impact on the properties of the BBCs. KOH-biobased carbon material (KOH-BBC) had a higher specific surface area (SBET), equal to 1067 m2 g−1, larger pore volume (0.558 cm3 g−1), more mesopores, and a more hydrophilic surface than ZnCl2-BBC. However, the carbon yield for KOH-BBC was 63% lower than for ZnCl2-BBC. Batch adsorption experiments were performed to evaluate the ability of the two BBCs to remove two dyes, reactive orange 16 (RO-16) and reactive blue 4 (RB-4), and treat synthetic effluents. The general order model was most suitable for modeling the adsorption kinetics of both dyes and BBCs. The equilibrium parameters at 22 °C were calculated using the Liu model. Upon adsorption of RO-16, Qmax was 90.1 mg g−1 for ZnCl2-BBC and 354.8 mg g−1 for KOH-BBC. With RB-4, Qmax was 332.9 mg g−1 for ZnCl2-BBC and 582.5 mg g−1 for KOH-BBC. Based on characterization and experimental data, it was suggested that electrostatic interactions and hydrogen bonds between BBCs and RO-16 and RB-4 dyes played the most crucial role in the adsorption process. The biobased carbon materials showed high efficiency for removing RO-16 and RB-4, comparable to the best examples from the literature. Additionally, both the KOH- and ZnCl2-BBC showed a high ability to purify two synthetic effluents, but the KOH-BBC was superior.

Pyrolysis transforms bulky and heterogeneous lignocellulosic biomass into more easily-handled oils that can be upgraded into bio-based transportation fuels. Existing systems for monitoring pyrolysis processes and characterizing their products rely on slow and time-consuming wet chemical analyses. On-line near-infrared (NIR) spectroscopy could potentially replace such analyses, providing real-time data and reducing costs. To test the usefulness of NIR methods in characterizing pyrolysis oils and processes, biomass from conifers, Salix, and reed canary grass was milled and pyrolyzed at 675, 750, and 775 °C. Two separate pyrolytic fractions (aerosol and condensed) were produced in each experiment, and NIR spectra were collected for each fraction. Multivariate modelling of the resulting data clearly showed that the samples’ NIR spectra could be used to accurately predict important properties of the pyrolysis oils such as their energy values, main organic element (C, H and O) contents, and water content. The spectra also contained predictive information on the samples’ origins, fraction, and temperature treatment, demonstrating the potential of on-line NIR techniques for monitoring pyrolytic production processes and characterizing important properties of pyrolytic oils from lignocellulosic biomass.

Ash formation during thermochemical conversion of biomass-based pellets influences both char conversion rates and ash-related operational problems. The objective of the present study was to provide ...

Volatile organic compound (VOC) off-gassing behavior of thermally treated biomass intended for bioenergy production has recently been shown to be vastly different from that of untreated biomass. Simple measures to reduce emissions, such as controlled ventilation and prolonged storage time, have been suggested but not yet studied in detail. In the present study, we monitored how VOC off-gassing was reduced over time (24–144 h) in enclosed storage with and without ventilation. Steam-exploded bark was collected directly from a pilot-scale steam explosion plant as well as before and after subsequent pelletizing. Active Tenax-TA absorbent sampling of VOCs was performed from the headspaces of a bench-scale sample storage setup. The impact of storage time and ventilation on VOC levels was evaluated through multivariate statistical analysis. The results showed that relative VOC concentrations in the headspace were reduced by increased storage time, with heavier VOCs reduced at a higher rate. VOC composition was n...

Formation of hazardous gases during transport and storage of biomass for large-scale bioenergy production is an important safety concern. While off-gassing has been addressed in numerous studies fo ...

The addition of Ca-containing compounds can reduce mass loss from agricultural biomass during storage. The resulting alkaline environment is detrimental to microorganisms present in the material. T ...

The quest to develop flexible membrane-like supercapacitors to be applied in advanced electronic devices with a flexible structure is important for the modern world. In this study, we developed biomass-based supercapacitors by depositing activated carbon on an eggshell membrane and subsequently coating these with polypyrrole in a two-step procedure. The competition between the electrical double layer capacitance (EDLC) from activated carbon and the pseudocapacitance (PC) for the hybrid device is controlled by varying the amount of polypyrrole (PC component) in a time-dependent polymerization process. An areal capacitance of 172.5 mF cm−2, a corresponding energy density of 4.73 W h kg−1, and power density of 320.8 W kg−1, with a 60% retention even after 1000 cycles were obtained for samples prepared with the polymerization of polypyrrole on the activated carbon (incorporation of an active layer of 3.18 mg cm−2).

The phosphorus and potassium contents of the char obtained from thermal conversion of forest residues can limit its utilization as an alternative fuel and reducing agent to substitute coal/coke in the steelmaking industry. In this study, ash transformation and release of K and P during single-pellet thermal conversion of different types of forest residues (i.e., bark, twigs, and bark+twigs) were investigated with the aid of a vertical tube furnace (Macro-TGA) at different temperatures (i.e., 600, 800, and 950 °C) and within and after different fuel conversion stages, i.e., devolatilization and char gasification. The residual char before and after full devolatilization, and ash after char gasification were characterized by SEM-EDS, XRD, and ICP-OES with the support of thermochemical equilibrium calculations. The concentrations of K (7970–19500 mg/kg) and P (1440–4925 mg/kg) in the char produced after devolatilization were more than four times higher than in coke and pulverized coal frequently used in metallurgical processes. A low amount of P and K (≤15%) were released from all fuels. K and P were evenly distributed within the char residues, and no crystalline compounds containing K and P were found. In ash residues of bark, K was found in K2Ca2(CO3)3, and K2Ca(CO3)2. K in ash residues from twigs and bark+twigs was mainly found in the amorphous part of ash, most likely in the form of K-Ca rich silicates. Apatite was found as the main P crystalline compound in all ashes at all temperatures. Estimations show that a release of more than 80% is needed for the studied forest residual assortments to reach K and P concentrations typical of blast furnace coals and cokes.

[Departement_IRSTEA]Ecotechnologies [TR1_IRSTEA]INSPIRE [ADD1_IRSTEA]Équiper l'agriculture; International audience; Geological and archaeological analysis of stone masonries in standing structures helps reveal information about use of natural resources. At the same time, the study of historical materials is useful for conservators and cultural heritage management. Geochemical and petrographic analysis of building material types is usually done through destructive analysis on a few selected samples and can be problematic due to the costs of operations and the size of buildings themselves. This paper demonstrates that the combination of hyperspectral imaging portable Near Infrared (NIR) spectroscopy and Energy Dispersive X-ray Fluorescence (ED-XRF) spectroscopy can be useful for analysing types of raw materials used in distinct construction phases of the inner defensive wall in the citadel of Carcassonne (Aude, France). Stratigraphic analysis of the architecture, short-range spectral remote sensing and portable ED-XRF measurements were combined in an interdisciplinary approach to classify sandstone elements. The experimental protocol for in situ non-destructive analysis and classification of the masonry types allows the investigation of the monument in a diachronic perspective, collecting information to delineate raw materials varieties and their use or re-use through time.

Ash formation during single-fuel pellet combustion of wheat straw at 700 and 1000 °C was studied throughout fuel conversion by quench cooling and analysis at different char conversion degrees. The combination of X-ray microtomography analysis and scanning electronic microscopy with energy-dispersive X-ray spectroscopy showed that ash accumulated in rigid net structures at 700 °C with streaks or small beads surrounding the char, and the pellet mostly maintained its size during the entire fuel conversion. At 1000 °C, the ash formed high-density melts that developed into bubbles on the surface. As the conversion proceeded, these bubbles grew in size and covered parts of the active char surface area, but without entirely blocking the gas transport. The successive char conversion dissolved increasing amounts of calcium in the potassium silicate melts, probably causing differences in the release of potassium to the gas phase. Similarities were found with slag from a combustion experiment in a domestic boiler, with regard to relative composition and estimated and apparent viscosity of the slag. Complete char encapsulation by ash layers limiting char burnout was not found at the single pellet level, nor to any greater extent from the experiment performed in a small domestic boiler. Bio4Energy

This study proposes a method for the classification of lithic raw materials by means of hyperspectralimaging, a non-destructive fast analytical technique. The information potential of this approach wastested on a dwelling site dated to mid-late Mesolithic (7200–5800 BP) at Lillsjön, Ångermanland,Sweden. A dataset of lithic tools and flakes (2612 objects) made of quartz and quartzite, wasanalyzed using a shortwave infrared hyperspectral imaging system. The classification of the rawmaterials was performed applying multivariate statistical models. A random test set of 55artefacts was selected, classified according to spectral signature and divided into categoriescorresponding to different geological materials. The same test set was analyzed with EnergyDispersive X-Ray Fluorescence (ED XRF) to validate the classification. The entire dataset of lithicscollected on the site was then classified applying a SIMCA model. The distribution of items onthe site was visualized in a 3D GIS platform according to their geological characteristics tohighlight patterns that could indicate different use of the space and dynamics of raw materialssupply over time. Mobima; Bio4Energy

Torrefaction, pyrolysis and gasification are of interest to convert lignocellulosic biomass into fuels and chemicals. These techniques involve thermal treatment at low partial pressures of oxygen. However, little is known about the transformation of ash elements during these processes. The phase transition of the major ash element calcium (Ca) was therefore studied with powder from pine as biomass model treated at temperatures 300–800 °C under atmospheres of 100% N2, 3% O2 and 6% O2 and thermodynamic equilibrium modelling. For evaluation, X-ray powder diffraction and synchrotron Ca K-edge X-ray absorption near edge structure (XANES) spectroscopy in combination with linear combination fitting and reference compounds was used. The results indicated that the most abundant Ca-containing species in the untreated material was thermally unstable Ca oxalate (CaC2O4) primarily decomposing into Ca phases dominated by carbonates at temperatures up to 600 °C. Double carbonates of calcium and potassium were observed in the form of fairchildiite/butscheliite (K2Ca(CO3)2), and these phases were stable over the low temperature range studied. Hydroxyapatite (Ca5(PO4)3OH) was expected to be present and thermally stable over the entire temperature interval and was found in untreated material. At temperatures above 600 °C calcium oxide (CaO) was formed. The amount of oxygen had little effect on the phase transitions. The results of thermodynamic modeling were in agreement with XANES showing that this is a versatile technique that can be applied to systems as complex as Ca phase transitions in thermally treated lignocellulosic biomass at low partial pressures of oxygen.

This study was performed to investigate if the process settings that give high pellet durability can be modelled from the biomass’ macromolecular composition. Process and chemical analysis data was obtained from a previous pilot-scale study of six biomass assortments that by Principal Component Analysis (PCA) was confirmed as representative for their biomass types: hardwood, softwood bark, short rotation coppice (SRC), and straw and energy crops. Orthogonal Partial Least Squares Projections to Latent Structures (OPLS) models were created with the content of macromolecules as factors and the die compression ratio and the feedstock moisture content at which the highest pellet durability was obtained as responses. The models for die compression ratio (R2X = 0.90 and Q2 = 0.58) and feedstock moisture content (R2X = 0.87 and Q2 = 0.60), rendered a prediction error for obtained mechanical durability of approximately ±1%-unit, each. Important factors for modelling of the die compression ratio were: soluble lignin (negative), acetyl groups (negative), acetone extractives (positive), and arabinan (positive). For modelling of the feedstock moisture content, Klason lignin (negative), xylan (positive), water-soluble extractives (negative), and mannan (negative), were the most influential. Results obtained in this study indicate that it is possible to predict optimal process conditions in pelletizing based on the macromolecular composition of the raw material. In practice, this would mean a higher raw material flexibility in the pellet factories through drastically reduced risk when introducing new raw materials.

The carbon matrix in cell walls of lignocellulosic plants has high recalcitrance to chemical and biological decomposition. Thermal treatments, such as torrefaction and pyrolysis are therefore of in ...

An innovative pellet burner cup (“BTC burner”) designed to enable the burning of ash-rich fuels in small-scale boilers (30–40 kW) was evaluated, with respect to slagging behavior, combustion perfor ...

Solid biomass as a biorefinery feedstock is physically and chemically heterogeneous which stress the need for rapid and accurate methods for characterization and classification. In this study, stem wood, hemp, grape and olive residues were characterized using X-ray fluorescence (XRF) spectroscopy and principal component analysis. XRF spectra were processed by partial least squares (PLSs) regression and used to construct calibration models for several important ash-related elements. The models for the ash’s phosphorous, aluminium and ash contents all had excellent predictive accuracy, with performance-to-deviation ratios above three. The models for the potassium, silica, calcium, sodium and magnesium content exhibited lower predictive accuracies. Relevant energy intervals (bins) were selected using interval PLS and variable importance on projection scores. In most cases, bin-selection increased the models’ predictive accuracy and facilitated their interpretation.

In a pelletizing experiment the three factors sawdust moisture content, steam conditioning of the sawdust, and storage time of the raw material, were varied in a full factorial design with a total of 34 experiments to evaluate the influences on the pelletizing process and the pellet quality when producing biofuel wood pellets from pine sawdust. Moisture content of the sawdust was found to be the dominant factor for the bulk density and for the pelletizer motor current, both showing low values at high moisture contents due to the lubricating property of water that lowers the friction in the pelletizing process. More complex models were obtained for mechanical durability and the amount of fines, where all factors and most interactions and squared terms were significant. In order to explain the effect of the sawdust moisture content and the storage time on these response factors, a qualitative model for the binding mechanism is suggested. In this model water is supposed to be actively involved in the binding mechanism as hydrogen bonded bridges. The increase in binding strength with storage time is explained by the reduction of extractive content which contain molecules that can block binding sites on the material surface. Optimum pellet quality was obtained when the storage time exceeded 120 days and within a range of sawdust moisture content of 11–13%.

A pilot scale pelletizing system (capacity: 300 kg/h) with integrated die temperature control was built and evaluated using reed canary grass as a model raw material. A pelletizing series was performed using a full factorial design having independent factors such as die temperature (35–65 °C), raw material moisture content (12–15% w.b.), and raw material temperature/steam conditioning (0–2 kg/h), with continuous or discontinuous feed layer formation as responses. Die temperature was the most influential parameter on feed layer formation and was negatively correlated to continuous feed layer formation. An immediate response, changing discontinuous production patterns into continuous was experienced when die temperature was lowered by the temperature control system. Further, a partial least squares discriminant analysis model, using the experimentally varied parameters, predicted continuous or discontinuous feed layer formation with 100% accuracy. Thus, die temperature control can be considered as a fast and efficient method for overcoming feed layer losses in pelletizing.

Forest-based biorefinery feedstocks are usually broken up into wood chips prior to any form of processing. These wood chips have a complex and highly variable composition, although they may look identical to an inexperienced observer. Some chips have high contents of valuable extractives. Therefore, it would be desirable to separate such chips that are rich in extractives. Various fractions of pine and spruce wood were used to acquire near infrared (1000–2498 nm) hyperspectral images in order to explore the usefulness of multivariate image analysis for detection and separation purposes. Multivariate modelling by image principal component analysis detected large variations in extractive content among wood chips of different biomass types, for example, sapwood, heartwood and knotwood. The extractive parts could be classified in the images and their content could be reasonably well predicted. Partial least squares (PLS) regression models could be made between collected spectra and measured extractive contents. These worked better for milled and homogenised bulk samples than for average image spectra. Regression coefficients showed that the C–H bonds in the spectra were responsible for the validity of the models. The average image PLS models could be used to make prediction images showing the location of the regions with high extractive content in knotwood. The results indicate that extremely rapid spectral-based fractionation could be used to separate tailored biomass streams of wood chips.

Sawdust of conifers as a by-product from saw mills is the most commonly used biomaterial for pellet production in Sweden today. Experiences from the biofuel pellet industry indicate that different ...

Ash-related problems have more than occasionally been observed in biomass-fired boilers and also recently in biopellet burners. These problems can lead to reduced reliability of the combustion syst ...

When Arctic charr Salvelinus alpinus from two diVerent stocks were fed live Neomysis integer, the upper thermal limits for feeding and growth were established in the range 21·5–21·8° C. These critical temperatures might have been underestimates, because fish tend to show increased sensitivity to handling at high experimental temperatures. In the second experiment, the proportion of feeding undisturbed charr from four stocks decreased initially as temperature was raised in steps from 18 to 22° C. At the lower temperatures, 18 and 20) C, almost all fish resumed feeding, but the recovery time was longer and more fish ceased to feed at 20) C than at 18° C. When the temperature was increased to 21° C, 50% of the fish ceased feeding permanently, and all fish ceased feeding within 2 days at 22° C. It is concluded that 0+ charr cease to feed and grow at c.21·5) C and that the critical temperatures for feeding and growth coincide.

In this study, pre-compaction was evaluated as a method to enhance stable reed canary grass pellet production. An experimental design of the factors raw material moisture content, steam addition, raw material bulk density, and die temperature was used to find production conditions for high quality pellets by multiple linear regression modelling of responses. Response variables being modelled were variability of pelletizer current (as a measurement of uneven production), pellet bulk density, and pellet durability. By pre-compacting the raw material from a bulk density of 150 kg/m 3 to 270 kg/m 3 , continuous production could be obtained at minimum raw material moisture content of 13.8%. Bulk density and durability were both highly correlated to raw material moisture content, but showed different optima. Multiple response optimization was used to target process settings for production of high quality reed canary grass pellets with bulk density >650 kg/m 3 and durability >97.5%.