Concentration Of OH Groups Research Articles

Investigation of uniformity in fused quartz crucibles for Czochralski silicon ingots

As there is an increased demand for monocrystalline silicon based solar cells, there is an increased interest in stronger and more durable fused quartz crucibles used in the Czochralski process. In this study we focused on the uniformity of hydroxyl impurities in these crucibles, and its potential influence on viscosity of the crucible by combining data from IR-microscopy and a self-made viscosity measurement setup. A half of a fused quartz crucible manufactured from two types of sands was studied, the OH groups content was mapped, and the viscosity at 1500 °C was measured. Local variations in the OH groups content of on average 26.7 ppm difference between the top and the bottom of the crucible were detected. The viscosity measurements further confirmed the crucible’s inhomogeneity as no clear trends or direct correlations to the OH groups content were observed. The correlation between the different sand types used for crucible manufacturing and the OH groups content was also investigated in four samples originating from four different crucibles. Two different trends in the OH groups distribution were found: while two of the studied crucibles showed an increased OH groups content in the boundary between the bubble free and the bubble containing layer, the other two showed an increased and maximum OH groups content in the bubble containing layer, and the link between the sand types and the OH groups content was confirmed. The source of the local inhomogeneities and the two different trends of OH groups distribution can possibly be attributed to the sand quality, the sand particle size, and the difference in the manufacturing process, such as thermal history or distribution of sand.

Procuring the polysaccharides with anti-inflammatory bioactivity from Russula vinosa Lindblad by citric acid extraction

Russula vinosa Lindblad is a wildly edible fungus that has been used as the health food due to its high content of bioactive constituents. This study investigated the anti-inflammatory bioactivity of two kinds of low-molecular-weight polysaccharides (CA-S and CA-L) extracted by citric acid (CA) from Russula vinosa Lindblad. The structure of CA-S and CA-L were identified using different characterization techniques. Structural characterization revealed that both CA-S and CA-L possessed a similar structure for the backbone but differed in the substitution sites and residues. CA-S and CA-L demonstrated the ability to ameliorate the damage of intestinal tissue in dextran sulfate sodium (DSS)-induced ulcerative colitis mice in vivo, the DAI values of CA-S and CA-L fed mice decreased by 36.84% and 31.58% respectively. This might be attributed to CA-S's higher Mw, increased content of OH groups, and an enriched mannose fraction. Immuno-analysis revealed that CA-S better reduced inflammation and oxidative-state-related stress by scavenging the endogenous reactive oxygen species through the activation of Nrf2 and suppression of the NFκB signaling pathways.

The influence of the volume concentration of hydrogen on the fine structure of the IR absorption spectra and conductivity features in congruent LiTaO3 crystals

A new method for changing the volume concentration of hydrogen in congruent LiTaO3 (lithium tantalate, LT) crystals has been studied. It has been established that pre-treatment of the sample in adipic acid significantly increases the volumetric concentration of hydrogen in the sample during subsequent annealing in a humid atmosphere at a relatively low annealing temperature. First of all, this preserves the LT single crystal in a single-domain state. In contrast to known methods for increasing the volumetric concentration of hydrogen, the proposed method affects the absorption coefficient of the sample in the optical range less than for a congruent LiNbO3 crystal. It has been shown that the type of IR absorption spectrum of OH− groups and the defect structure of the LT crystal significantly depend on the volume concentration of hydrogen in the sample. The study also analyzed the reasons for this effect. The temperature dependences of the electrical conductivity of LT samples with different hydrogen concentrations have been studied. It has been shown that the type of electronic conductivity of LT samples changes when the concentration of OH groups in the crystal increases significantly.

Thermally Induced Reversible Changes in the 7200 cm–1 Absorption Band in a Fiber Light Guide with a High Concentration of OH Groups in the Core

Thermally Induced Reversible Changes in the 7200 cm–1 Absorption Band in a Fiber Light Guide with a High Concentration of OH Groups in the Core

Electron paramagnetic resonance and luminescence properties of Eu2+ in oxyfluoride barium borate glasses

The Eu-doped xBaO-(100-x)B2O3 and xBaF2-(100-x)B2O3 glasses were prepared by melting method under a reducing atmosphere, exhibiting broadband luminescence peaks of 4f65 d1→4f7 in the excitation range of 300–400 nm. PL, EPR, and XPS were used to analyze the effects of the Ba2+, F−, and Eu ion content on the Eu2+/Eu3+ ratio and Eu2+ emission wavelength and intensity. An excess of Ba2+ ions with a high optical basicity reduced the Eu2+/Eu3+ ratio and enhanced the ligand field strength surrounding the Eu2+ ions, decreasing the Eu2+ luminescence intensity and red-shifting the luminescence peak. The addition of F− had the effect of diminishing the optical basicity, decreasing the OH groups content and eliminating Eu2+ clusters, which not only mitigated the effects of the Ba2+ ions, but also significantly enhanced the luminescence intensity of Eu2+ ions. An increase in the Eu ion concentration led to a red-shift in the Eu2+ fluorescence, which was attributed to the nephelauxetic effect. Therefore, the luminescence color of these glass samples could be manipulated by adjusting the doping concentrations of Ba2+, F−, and Eu2+.

Impact of Bark-Sourced Building Blocks as Substitutes for Fossil-Derived Polyols on the Structural, Thermal, and Mechanical Properties of Polyurethane Networks.

The hydrophilic extractives isolated from black alder (Alnus glutinosa) bark through hot water extraction were characterized as novel renewable macromonomers capable of forming polyurethane (PU) networks based on a commercial polyisocyanate, with partial or complete replacement of petroleum-derived polyol polyether. The bark-sourced bio-polyol mainly consists of the xyloside form of the diarylheptanoid oregonin, along with oligomeric flavonoids and carbohydrates, resulting in a total OH group content of 15.1 mmol·g-1 and a molecular weight (Mn) of approximately 750 g∙mol-1. The 31P NMR data confirmed a similar proportion of aliphatic OH and phenolic groups. Three-component PU compositions were prepared using polyethylene glycol (Mn = 400 g∙mol-1), bio-polyol (up to 50%), and polymeric diphenylmethane diisocyanate, which were pre-polymerized in tetrahydrofuran (THF) solution with tin organic and tertiary amine catalysts. The resulting mixture was cast and subjected to thermal post-curing. Calculation and experimental data confirmed the crosslinking activity of the bark-sourced bio-polyol in PU, leading to an increase in glass transition temperature (Tg), a decrease in sol fraction yield upon leaching of cured PU networks in THF, a significant increase in Young's modulus and tensile strength. The macromonomers derived from bark promoted char formation under high temperature and oxidative stress conditions, limiting heat release during macromolecular network degradation compared to bio-polyol-free PU. It was observed that amine catalysts, which are active in urethane formation with phenolic groups, promoted the formation of PU with higher Tg and modulus at tensile but with less limitation of heat liberation during PU macromolecular structure degradation. The high functionality of the bark-derived bio-polyol, along with the equal proportion of phenolic and aliphatic OH groups, allows for further optimization of PU characteristics using three variables: increasing the substitution extent of commercial polyethers, decreasing the NCO/OH ratio, and selecting the type of catalyst used.

The Effect of Sample Preparation Techniques on Lignin Fourier Transform Infrared Spectroscopy.

The characterization and quantification of functional groups in technical lignins are among the chief obstacles of the utilization of this highly abundant biopolymer. Although several techniques were developed for this purpose, there is still a need for quick, cost-efficient, and reliable quantification methods for lignin. In this paper, three sampling techniques for fourier transform infrared (FTIR) spectroscopy were assessed both qualitatively and quantitatively, delineating how these affected the resultant spectra. The attenuated total reflectance (ATR) of neat powders and DMSO-d6 solutions, as well as transmission FTIR using the KBr pelleting method (0.5 wt%), were investigated and compared for eight lignin samples. The ATR of neat lignins provided a quick and easy method, but the signal-to-noise ratios in the afforded spectra were limited. The ATR of the DMSO-d6 solutions was highly concentration dependent, but at a 30 wt%, acceptable signal-to-noise ratios were obtained, allowing for the lignins to be studied in the dissolved state. The KBr pelleting method gave a significant improvement in the smoothness and resolution of the resultant spectra compared to the ATR techniques. Subsequently, the content of phenolic OH groups was calculated from each FTIR mode, and the best correlation was seen between the transmission mode using KBr pellets and the ATR of the neat samples (R2 = 0.9995). Using the titration measurements, the total OH and the phenolic OH group content of the lignin samples were determined as well. These results were then compared to the FTIR results, which revealed an under-estimation of the phenolic OH groups from the non-aqueous potentiometric titration, which was likely due to the differences in the pKa between the lignin and the calibration standard 4-hydroxybenzoic acid. Further, a clear correlation was found between the lower Mn and the increased phenolic OH group content via SEC analyses. The work outlined in this paper give complementary views on the characterization and quantification of technical lignin samples via FTIR.

Impact of lignin source on the performance of thermoset resins

A series of different technical hardwood lignin-based resins have been successfully synthesized, characterized, and utilised to produce thiol-ene thermoset polymers. Firstly, technical lignin was fractionated and allylated, whereafter it was crosslinked with a trifunctional thiol. Structural and morphological characteristics of the lignin fractions were studied by 1H NMR, 31P NMR, SEC, FTIR, DSC, TGA, and WAXS. The hardwood lignin fractions have a high content of C5-substituted OH groups. The WAXS studies on lignin fractions revealed the presence of two π-π stacking conformations, sandwiched (4.08–4.25 Å) and T-shaped (6.52–6.91 Å). The presence of lignin superstructures with distances/sizes between 10.5 and 12.8 Å was also identified. The curing reaction of the thermosets was investigated by RT-FTIR. Almost all thermosets (excepting one fraction) reached 95% of the thiol conversion in less than 17 h, revealing the enhanced reactivity of the allylated hardwood lignin samples.The mechanical properties of the thermosets were investigated by DMA. The curing performance, as well as the final thermoset properties, have been correlated to variations in chemical composition and morphological differences of lignin fractions. The described results clearly demonstrate that technical hardwood lignins can be utilized for these applications, but also that significant differences compared to softwood lignins have to be considered for material design.

Novel strategies to tune the color emission of Bi2Ti2-xZrxO7:Er3+,Yb+3 upconversion phosphors: Substituting Ti by Zr and annealing at high temperatures

Bi2Ti2-xZrxO7:Er3+,Yb3+ phosphors were synthesized with different content of Zr (X = 0–1.5) by combustion method at 550 °C, producing a mixture of Bi2Ti2O7/Bi4Ti3O12 phases. After increasing the synthesis temperature to 1000 °C, a pure Bi2Ti2O7 (BiTiO) phase was obtained as well as porous coalesced microparticles (2–10 µm) with pore sizes of 110–420 nm. Those samples produced green (548 nm)/red (655 nm) and NIR (1530 nm) emission bands after excitation with 980 nm and their color emission was tuned from green to yellow–red or viceversa using two strategies: i) by increasing the Zr content in the Bi2Ti2-xZrxO7:Er3+,Yb3+ host (from X = 0 to 1) or ii) by increasing the synthesis temperature from 550 to 1000 °C. Interestingly, the intensity of the NIR and red emission bands was enhanced with the content of OH groups on the surface of the BiTiO:Yb,Er phosphors.

Plasma Surface Modification of 3Y-TZP at Low and Atmospheric Pressures with Different Treatment Times.

The efficiency of plasma surface modifications depends on the operating conditions. This study investigated the effect of chamber pressure and plasma exposure time on the surface properties of 3Y-TZP with N2/Ar gas. Plate-shaped zirconia specimens were randomly divided into two categories: vacuum plasma and atmospheric plasma. Each group was subdivided into five subgroups according to the treatment time: 1, 5, 10, 15, and 20 min. Following the plasma treatments, we characterized the surface properties, including wettability, chemical composition, crystal structure, surface morphology, and zeta potential. These were analyzed through various techniques, such as contact angle measurement, XPS, XRD, SEM, FIB, CLSM, and electrokinetic measurements. The atmospheric plasma treatments increased zirconia's electron donation (γ-) capacity, while the vacuum plasma treatments decreased γ- parameter with increasing times. The highest concentration of the basic hydroxyl OH(b) groups was identified after a 5 min exposure to atmospheric plasmas. With longer exposure times, the vacuum plasmas induce electrical damage. Both plasma systems increased the zeta potential of 3Y-TZP, showing positive values in a vacuum. In the atmosphere, the zeta potential rapidly increased after 1 min. Atmospheric plasma treatments would be beneficial for the adsorption of oxygen and nitrogen from ambient air and the generation of various active species on the zirconia surface.

Comprehensive Study of the Chemical, Physical, and Structural Evolution of Molecular Layer Deposited Alucone Films during Thermal Processing

Thermal processing of molecular layer deposited (MLD) hybrid inorganic–organic alucone thin films produced porous and low-k materials. Alucone films were deposited by MLD using trimethyl aluminum and ethylene glycol at 120 °C. Changes in the film density and thickness during annealing were monitored using in-situ X-ray reflectivity and were compared to atomic layer deposited (ALD) alumina films. The chemical evolution of the as-deposited and annealed alucone films during post-deposition heating with and without UV was probed using infrared spectroscopy, Rutherford backscattering, nuclear reaction analysis, and 15N spectroscopy, providing a detailed understanding of the induced changes. The concentration of OH groups decreased after depositing 1 nm of alumina capping layer as a barrier to moisture uptake, which also decreased the etch rate in CF4/O2 plasma. The lowest dielectric constant of the processed alucone films (kmin = 4.75) was 25% lower than the lowest values measured in ALD alumina counterparts (kmin = 6.7). Large thickness decreases for alucone films were observed at ∼200 °C of anneal temperatures. Removal of retained organic components by thermal processing of MLD films is demonstrated to be a promising and versatile route to porous thin films for a wide range of applications including low dielectric constant materials.

Construction of an S-scheme TiOF2/HTiOF3 heterostructures with abundant OVs and O[sbnd]H groups: Performance, kinetics and mechanism insight

Developing efficient photocatalysts is of crucial significance for the development of photocatalysis techniques. In this work, an S-scheme alkaline-washed TiOF2/HTiOF3(OHTOF) heterostructures with abundant Oxygen vacancies (Ovs) and OH groups was successfully constructed and used to remedy antibiotic wastewater under simulated sunlight. The generation of HTiOF3 was induced by g-C3N4 regulation. The results displayed that OHTOF15 composite possessed the best photocatalytic performance, which could degrade 94.2% tetracyclinehydrochloride (TCH) at a rate speed constant of 1.077 min−1 in 2.5 h. The after-alkali-washing process increased the concentration of OH groups and Ovs defects, and greatly enlarged the surface area. The abundant Ovs and OH groups were conducive to the formation of free radicals’ and the transport of charge carriers. Compared with the pristine TiOF2, the absorption sidebands of OHTOF series were greatly red-shifted, which indicated that the increase of OH groups and the etching of the morphology of OHTOF further enhanced its visible-light harvesting ability. Furthermore, the metal cycle of the variable state of Ti4+/Ti3+ in OHTOF15 compensated for the charge balance and promoted the efficient separation of the carriers. Additionally, the apparent quantum efficiency (AQE) of the TCH photodegradation system based on Chemical Oxygen Demand (COD) removal efficiency was calculated to be 0.32%. It was confirmed that the electron transport path in TiOF2/HTiOF3 nanocomposites system followed the S-scheme type, which increased the charge carriers’ separation rate and maintained a strong redox capacity. This work could provide some enlightenment for the construction of the semiconducting heterojunction and controllable surface defects engineering.

Structure of the Poly(methyl methacrylate) Adsorbed Layer Determined by the Surface Chemistry of the Substrate

The adsorbed polymer layer on the inorganic solid surface is crucial in improving the physical properties of composite nanomaterials; therefore, the properties could be tuned by altering the structure of the adsorbed layer. We investigated poly(methyl methacrylate) (PMMA) adsorbed layers on SiO2–Si substrates by varying the hydroxyl (OH) group content on the substrate surface. The results indicated that the thicknesses of the flattened layer and loosely adsorbed layer decreased with decreasing OH group content and the flattened layer disappeared when the content was ∼31%. The OH groups controlled the formation of the adsorbed layer, providing anchor points through hydrogen bonding with the carbonyl groups in PMMA. With decreasing OH group content, fewer anchor points possibly prevented train conformation and the relatively stable loosely adsorbed chains still formed, which enhanced the segmental dynamics of the ultrathin PMMA film. These results provide novel insight into the role of surface chemistry in forming adsorbed polymer layers on substrates.

Formation conditions of quartz deposits in the Southern Urals: Fluid inclusion data and IR spectroscopy

Research subject. Quartz veins of the Svetlorechenskoye, Karayan, Gora Khrustalnaya and Tolstikha quartz deposits in the Southern Urals.Methods. An optical study of quartz was performed using an Olympus BX51 optical microscope. A fluid inclusion study was performed using a thermostage TMS-600 (Linkam) equipped with the LinkSys V-2.39 software and an Olympus BX51 optical microscope (South Urals State University, Miass). The fluid composition in the inclusions was estimated from eutectic temperatures. Fluid salinity was calculated based on the melting temperatures of crystalline pha ses. Registration of infrared spectra was carried out using an infrared Fourier spectrometer Nicolet-6700 Thermo Scientific (SU FRC MG UB RAS, Miass). The spectra were processed using the OMNIC Thermo Nicolet software package and the Peakfit program. The extinction coefficients for calculating the concentration of molecular water and OH-groups were used from.Results. The veins are composed of coarse-grained milky-white quartz. The fluid inclusion data shows that the quartz veins were deposited from similar in composition NaCl-H2O fluids with salinities of 3–9 wt % NaCl eq. and at temperatures ranging from 100 to 280°C. Quartz in the Tolstikha deposit was deposited at the highest temperatures. According to IR spectroscopy data, quartz in the studied deposits is characterized by high contents of molecular water and average concentrations of Al-OH groups. According to the content of OH-groups, quartz in the Tolstikha deposit approaches industrial granulated quartz used in the production of high-purity quartz concentrates.Conclusions. Quartz veins in the studied deposits formed at temperatures ranging from 100 to 280°C. The salinity of inclusions in quartz ranged from 10 to 3.5 wt % NaCl eq. Mineral-forming fluids were of Na-chloride or Na-K-chloride composition, which indicates quartz crystallization during the post-diagenetic (metamorphic) transformation of rocks. Quartz in the studied deposits is characterized by a specific ratio of water and Al-OH, which is associated with the conditions of deposit formation and incompleteness of quartz metamorphism processes therein.

Synthesis of Multifunctional Oligomethylsilsesquioxanes by Catalyst-Free Hydrolytic Polycondensation of Methyltrimethoxysilane under Microwave Radiation

The catalyst-free hydrolytic polycondensation of methyltrimethoxysilane under microwave radiation has been studied. The effect of molar ratios of the reagents (MTMS/H2O = 1/0.5-1/9), radiation power (20-300 W), temperature (30-50 °C) and duration of exposure (2.5-90 min) on the course of the process is considered. It has been shown that the use of microwave radiation promotes the activation of the process, and almost complete conversion of the monomer can be achieved in 5 min at 30 °C, 20 W and an MTMS/H2O ratio of 1/3. The optimal radiation power for the maximum conversion of the monomer and MeO-groups is in the range from 20 to 100 W. An increase in the water amount, the duration and temperature of the process contribute to an increase in the monomer conversion, a decrease in the content of residual MeO-groups and the yield of non-volatile oligomethylsilsesquioxanes. The limits of this approach using to the synthesis of multifunctional branched polyorganosilsesquioxanes are determined. Depending on the process conditions, homogeneous water-alcohol solutions of oligomethylsilsesquioxane with a concentration of 20 to 50 wt.% can be obtained. The OH-group content and the molecular weight of the obtained oligomers vary from 10 to 30 wt.% and from 1000 to 600 Da, respectively.

Эволюция структурных и точечных дефектов в кварцевом стекле, подвергнутом тонкому отжигу

The silica glass with a high content of OH groups was synthesized by the high-temperature hydrolysis of SiCl4 in a flame of oxyhydrogen torch and subjected to fine annealing. A combination of the photoluminescence and IR reflection spectroscopy was applied to assess the evolution of the ensemble of structural defects in the bulk and surface layer over the course of annealing carried out at 480 ˚C. The marked decrease of the defect concentration was observed in the bulk at all time expositions in the range 2 to 72 hours. However, in a thin surface layer, the decrease of the concentration of silanol groups Si-OH formed in the process of synthesis was detected. Decay of these groups results in the silicate network consolidation that led to the forming of the superficial layer characterized by an elevated microhardness.

Organosolv Lignin as a Green Sizing Agent for Thermoformed Pulp Products.

The purpose of this study was to investigate the use of organosolv lignin as a sizing agent for thermoformed pulp products as a sustainable material with improved water resistance. For this purpose, an in-house-produced organosolv lignin from softwood (Norway Spruce) was mixed with bleached and unbleached chemi-thermomechanical pulp fibers. In addition, the isolated organosolv lignin was characterized by ATR-FTIR spectroscopy, size-exclusion chromatography, and thermogravimetric analysis. The analysis showed that organosolv lignin was of a high purity and practically ash-free, exhibiting low molecular weight, a glass transition temperature below the thermoforming temperature, and a high content of phenolic OH groups. The mechanical properties and water resistance of the organosolv lignin-sized thermoformed pulp materials were measured. A small decrease in strength and an increase in stiffness and density were observed for the lignin-sized thermoformed materials compared to the reference, that is, unsized materials. The addition of organosolv lignin decreased the wettability and swelling of the thermoformed product. These results are due to the distribution of organosolv lignin on the surface, filling in the pores and cavities, and providing a tighter fit within the thermoformed materials. In conclusion, the results from our study encourage the use of organosolv lignin as a sizing additive to thermoformed products, which can improve the water resistance to use it in sustainable packaging applications.

IR-SPECTROSCOPIC STUDY OF WATER AND HYDROGEN DEFECTS IN INDUSTRIAL QUARTZ TYPES OF KARELIA (RUSSIA)

The results of an IR spectroscopic study of the content of water and hydrogen defects in hydrothermal and pegmatite quartz from quartz-vein occurrences in Karelia (North-West Russia), considered as a promising source of high-purity quartz raw materials, are presented. It is shown that the main amount of water in the analyzed quartz is in molecular form, and OH groups associated with aluminum, lithium, and boron trace elements in the quartz lattice are also identified. Granular quartz with the lowest content of molecular water and OH-groups is the most preferred for use as a high-purity quartz raw material.

Lignin molecular design to transform green manufacturing

<h2>Summary</h2> Lignin is the most abundant phenolic biopolymer on earth, representing an abundant feedstock for green manufacturing. Nevertheless, the diverse chemical linkages, heterogeneous functional groups, variable molecular weights, and amphiphilic structures all prevent the synthesis of fungible materials from lignin, leaving it as a predominantly low-value resource. On the basis of structure-property relationship, we synergistically overcome these challenges by chemical design of a type of lignin, high-molecular weight esterified linkage lignin (HiMWELL), with more uniform esterified linkages, larger molecular weight, and much lower OH group content via interunit substucture replacement. HiMWELL transforms lignin into a precursor for manufacturing renewable materials with drastically improved properties and functionality. The HiMWELL-based carbon fiber achieved a record tensile strength and better mechanical properties than the control polyacrylonitrile carbon fiber. HiMWELL also uniquely improved mechanical properties of the recyclable polymer blends and achieved UV-shading effects.

Acacia Wood Fractionation Using Deep Eutectic Solvents: Extraction, Recovery, and Characterization of the Different Fractions.

The selective extraction and recovery of different lignocellulosic molecules of interest from forestry residues is increasing every day not only to satisfy the needs of driving a society toward more sustainable approaches and materials (rethinking waste as a valuable resource) but also because lignocellulosic molecules have several applications. For this purpose, the development of new sustainable and ecologically benign extraction approaches has grown significantly. Deep eutectic solvents (DESs) appear as a promising alternative for the processing and manipulation of biomass. In the present study, a DES formed using choline chloride and levulinic acid (ChCl:LA) was studied to fractionate lignocellulosic residues of acacia wood (Acacia dealbata Link), an invasive species in Portugal. Different parameters, such as temperature and extraction time, were optimized to enhance the yield and purity of recovered cellulose and lignin fractions. DESs containing LA were found to be promising solvent systems, as the hydrogen bond donor was considered relevant in relation to lignin extraction and cellulose concentration. On the other hand, the increase in temperature and extraction time increases the amount of extracted material from biomass but affects the purity of lignin. The most promising DES system, ChCl:LA in a ratio of 1:3, was found to not significantly depolymerize the extracted lignin, which presented a similar molecular weight to a kraft lignin. Additionally, the 31P NMR results revealed that the extracted lignin has a high content of phenolic OH groups, which favor its reactivity. A mixture of ChCl:LA may be considered a fully renewable solvent, and the formed DES presents good potential to fractionate wood residues.