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Stalk lodging contributes to significant crop yield losses. Therefore, understanding the biomechanical strength and structural rigidity of grain stalks can contribute to improving stalk lodging resistance in crops. From the structural constituents of the stalk, the rind provides the principal structure, supporting cells against tension and bending loads. In this work, the biomechanical and viscoelastic behavior of the rind from the internodes of two sweet sorghum varieties (Della and REDforGREEN (RG)), grown in two different growing seasons, were evaluated by three-point micro-bending tests using a dynamic mechanical analyzer (DMA). In addition, the chemical composition of rinds and the microfibril angle (MFA) of the cell wall were determined using XRD. The results revealed that the biomechanical behavior of Della varieties was stiffer and more resistant to loads than that of RG varieties. Two features of the rind biomechanical properties, flexural modulus (FM) and flexural strength (FS), showed a significant reduction for RG. Particularly, a reduction in FS of 16–37% and in FM of 22–41% were detected for RG1. Changes in the stalks' rind biomechanical properties were attributed to cell wall components. Total lignin and glucan/cellulose contents were positively correlated with the FM and FS of the rind. Subsequently, an increase in the two cell wall components drove an increase in stiffness. Furthermore, the MFA of the rind was also found to influence the rind strength. [ABSTRACT FROM AUTHOR]

This study examined the use of softwood mill residues (50–90%) with two thermosetting resins (i) urea-formaldehyde (UF) and (ii) phenol-resorcinol-formaldehyde (PRF) resin, for potential use in additive manufacturing (AM) of wood composite materials. The curing behavior of these blends was evaluated using differential scanning calorimetry and dynamic rheology. Curing kinetics was determined using the Kissinger and Cranes method. The presence of wood fibers reduced the curing peak temperatures for both resin blends at the same heating rates but curing peak temperatures increased with heating rates. The activation energy (Ea) increased with the addition of wood for the wood-PRF blends but reduced for the wood-UF blends in comparison to the neat resins. Ea values were 51 and 271 kJ/mol for PRF and wood-PRF samples and 100 and 367 kJ/mol for UF and wood-UF samples. Frequency sweep flow curves of the green wood-resin blends showed shear thinning behaviors with viscosity values between 103–108 Pa.s at 30°C. Mechanical properties of the wood-resin composites generally showed a reduction in flexural modulus with an increase in wood content. Wet wood (50%)-PRF blend was successfully extruded and showed promise for use in AM; however, the wood-UF blend was not successful. [ABSTRACT FROM AUTHOR]

This study investigated the efficacy of lauric arginate (LAE) as a potential preservative against wood deteriorating fungi. First, the antifungal properties of LAE against two brown rot fungi, Gloeophyllum trabeum (G.t.) and Rhodonia placenta (R.p.), and two white rot fungi, Trametes versicolor (T.v.) and Irpex lacteus (I.l.) were examined using malt-agar media as substrate. Then the biological resistance of LAE-treated wood specimens (10, 20, and 25 % LAE solutions) was tested following American Wood Protection Association (AWPA) E10 soil-block test procedures. The in vitro study showed LAE actively inhibited the growth of all the fungi tested compared to growth in control plates but there were no considerable changes observed in the morphology of fungi hyphae. Wood impregnated with LAE showed increased weight percent gain as a function of treatment concentration. Characterization of LAE-treated wood on a thermogravimetric analyzer showed LAE shifted the thermal degradation temperatures to lower stages but did not significantly improve the thermal stability of the treated specimen. LAE in wood significantly suppressed fungus growth, leading to decreased mass loss but it also leached out from wood specimens during fungi exposure. [ABSTRACT FROM AUTHOR]

The aim of this study was to evaluate the use of waste natural fibers from milled hop bines and hemp stalks, without chemical treatment, and compare them to a commercial wood fiber for use in wood–plastic composite (WPC) materials. The fibers were characterized (density, fiber size and chemical composition). WPCs were produced by the extrusion of a blend of fibers (50%), high-density polyethylene (HDPE) and coupling agent (2%). The WPCs were characterized for their mechanical, rheological, thermal, viscoelastic and water resistance properties. Pine fiber was about half the size of hemp and hop fibers and thus had a higher surface area. The pine WPC melts had a higher viscosity than the other two WPCs. Additionally, the tensile and flexural strengths of the pine WPC were higher than those of hop and hemp WPCs. The pine WPC was also shown to have the least water absorption followed by hop and hemp WPCs. This study highlights that different lignocellulosic fibers influence their WPC properties. The properties of the hop- and hemp-based WPCs were comparable to commercial WPCs and can be improved by further milling/screening the fibers to a smaller particle size (volumetric mean of ~88 μm) to increase their surface area, fiber–matrix interactions and improve stress-transfer. [ABSTRACT FROM AUTHOR]

Despite its massive potential, Raman imaging represents just a modest fraction of all research and clinical microscopy to date. This is due to the ultralow Raman scattering cross-sections of most biomolecules that impose low-light or photon-sparse conditions. Bioimaging under such conditions is suboptimal, as it either results in ultralow frame rates or requires increased levels of irradiance. Here, we overcome this tradeoff by introducing Raman imaging that operates at both video rates and 1,000-fold lower irradiance than state-of-the-art methods. To accomplish this, we deployed a judicially designed Airy light-sheet microscope to efficiently image large specimen regions. Further, we implemented subphoton per pixel image acquisition and reconstruction to confront issues arising from photon sparsity at just millisecond integrations. We demonstrate the versatility of our approach by imaging a variety of samples, including the three-dimensional (3D) metabolic activity of single microbial cells and the underlying cell-to-cell variability. To image such small-scale targets, we again harnessed photon sparsity to increase magnification without a field-of-view penalty, thus, overcoming another key limitation in modern light-sheet microscopy [ABSTRACT FROM AUTHOR]

Agriculture generates non-recyclable mixed waste streams, such as plastic (netting, twine, and film) and lignocellulosic residues (bluegrass straw/chaff), which are currently disposed of by burning or landfilling. Thermochemical conversion technologies of agricultural mixed waste (AMW) are an option to upcycle this waste into transportation fuel. In this work, AMW was homogenized by compounding in a twin-screw extruder and the material was characterized by chemical and thermal analyses. The homogenized AMW was thermally and catalytically pyrolyzed (500–600 °C) in a tube batch reactor, and the products, including gas, liquid, and char, were characterized using a combination of FTIR, GC-MS, and ESI-MS. Thermal pyrolysis wax products were mainly a mixture of straight-chain hydrocarbons C7 to C44 and oxygenated compounds. Catalytic pyrolysis using zeolite Y afforded liquid products comprised of short-chain hydrocarbons and aromatics C6 to C23. The results showed a high degree of similarity between the chemical profiles of catalytic pyrolysis products and gasoline. [ABSTRACT FROM AUTHOR]

Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) with various 3-hydroxyvalerate (3HV) contents biosynthesized by mixed microbial consortia (MMC) fed fermented dairy manure at the large-scale level was assessed over a 3-month period. The thermal, mechanical, and rheological behavior and the chemical structure of the extracted PHBV biopolymers were studied. The recovery of crude PHBV extracted in a large Soxhlet extractor with CHCl3 for 24 h ranged between 20.6% to 31.8% and purified to yield between 8.9% to 26.9% all based on original biomass. 13C-NMR spectroscopy revealed that the extracted PHBVs have a random distribution of 3HV and 3-hydroxybutyrate (3HB) units and with 3HV content between 16% and 24%. The glass transition temperature (Tg) of the extracted PHBVs varied between −0.7 and −7.4 °C. Some of the extracted PHBVs showed two melting temperatures (Tm) which the lower Tm1 ranged between 126.1 °C and 159.7 °C and the higher Tm2 varied between 152.1 °C and 170.1 °C. The weight average molar mass of extracted PHBVs was wide ranging from 6.49 × 105 g·mol−1 to 28.0 × 105 g·mol−1. The flexural and tensile properties were also determined. The extracted polymers showed a reverse relationship between the 3HV content and Young's modulus, tensile strength, flexural modulus, and flexural strength properties. [ABSTRACT FROM AUTHOR]

Plastic waste accumulation has been growing due to the increase in plastic generation and the lack of infrastructure for recycling. One of the approaches is to treat the mixed plastic waste (MPW) through thermal processes to produce feedstocks for other applications. However, the presence of polyvinyl chloride (PVC) in MPW would produce HCl during processing and has negative impacts (emission, catalyst poisoning, etc.). In addition, due to the high heterogeneity of MPW, it is difficult to generate consistent experimental data. In this study, MPW was homogenized through double compounding–extrusion and then formed into a sheet to be treated at 400 °C. The solid products at various mass losses were characterized by heat and chlorine content, Fourier-transform infrared (FTIR) spectroscopy, and elemental composition analysis. It was found that the thermal degradation of MPW started at ~260 °C. The chlorine removal efficiency increased with mass loss and reached an asymptotic value of ~84% at ~28% mass loss, and the remaining chlorine can be attributed to inorganic sources. A PVC de-chlorination model was developed for MPW using TGA data for PVC and MPW to determine organic chlorine removal efficiency. These results show that PVC de-chlorination was not affected by other plastics at this temperature. As the mass loss increases, the heat content first increases and then decreases. It was found that mass loss is a universal parameter for organic chlorine removal efficiency and heat content. The elemental composition analysis and FTIR spectroscopy also shed more light into the chemical changes during MPW thermal degradation. [ABSTRACT FROM AUTHOR]

A novel route to adamantane substituted diene copolymers is demonstrated using emulsion polymerization, with an improved monomer synthesis. Heterogenous dehydration of 2‐(1‐adamantyl)‐3‐buten‐2‐ol using Amberlyst®‐15 cationic exchange resin at ambient temperature gave 2‐(1‐adamantyl)‐1,3‐butadiene (1) in excellent yield and presents an attractive alternative monomer synthesis route. Emulsion polymerization of 1 and mixtures of 1 and isoprene was carried out at room temperature using redox pair, hydroperoxide initiator. All poly(1) and poly(1‐ran‐isoprene) samples were soluble in common organic solvents and exhibited high 1,4‐microstructure. A continuous increase in glass transition temperature from −63 to 172°C was observed by increasing the ratio of 1 in the comonomer feed of poly(1‐ran‐isoprene), and Tg values were in good agreement with the Fox equation. After complete hydrogenation to poly(1‐vinyladamantane‐alt‐ethylene‐ran‐propylene‐alt‐ethylene), a continuous increase in Tg was observed from −55 to 152°C. The high solubility and improved access to 2‐(1‐adamantyl)‐1,3‐butadiene opens the door to exploration of diene polymers with enhanced high temperature properties. [ABSTRACT FROM AUTHOR]

The aim of this study was to explore the application of deuterium (D) labeled glucose-D 7 as Raman-tag in Yarrowia lipolytica to assess triacyl glycerides (TAG) biosynthesis. Cells were grown in N depleted media in: (i) glucose in H 2 O (control), (ii) glucose-D 7 in H 2 O and (iii) glucose-D 7 in D 2 O, and the resulting biomass and lipids quantified. Infrared and Raman spectroscopies showed the incorporation of D with the presence of a C-D stretching bands in the silent region (1800–2600 cm−1) for cells grown in glucose-D 7 in H 2 O and glucose-D 7 in D 2 O as compared to the control. Fatty acid methyl ester analysis of cells grown in the three media showed significant differences in lipid profiles. Cells grown on glucose-D 7 in H 2 O and glucose-D 7 in D 2 O showed unequivocally D incorporation in fatty acids and TAG by mass spectrometry. Higher D incorporation was observed when cells were grown in D 2 O than H 2 O. Deuterium was also incorporated into the cell wall polysaccharides. [Display omitted] • Deuterium was incorporated in Yarrowia lipolytica cells that were fed glucose-D 7. • Deuterium was incorporated in both the lipids and cell wall polysaccharides. • Higher levels of D were observed when using D 2 O versus H 2 O. • The lipids and polysaccharides were analyzed by Raman, FTIR, GC-MS and ESI-MS. [ABSTRACT FROM AUTHOR]

This study provides an extensive investigation on the kinetics, combustion characteristics, and thermodynamic parameters of the thermal degradation of guinea grass (Megathyrsus maximus) in N2-pyrolytic and oxidative atmospheres. A model-fitting technique and three different iso-conversional techniques were used to investigate the kinetics of the thermal process, after which an analysis of the combustion characteristics and thermodynamic parameters was undertaken. Prior to this, experiments on the physico-chemical characterization, thermogravimetric, and spectroscopic analyses were carried out to provide insight into the compositional structure of the guinea grass. The volatile matter, fixed carbon, and total lignin contents by mass were 73.0%, 16.1%, and 21.5%, respectively, while the higher heating value was 15.46 MJ/kg. The cellulose crystallinity index, determined by XRD, was 0.43. The conversion of the GG in air proceeded at a relatively much higher rate as the maximum mass-loss rate peak in a 20 K/min read was −23.1 and −12.3%/min for the oxidative and the pyrolytic, respectively. The kinetics investigation revealed three distinctive stages of decomposition with their corresponding values of activation energy. The average values of activation energy (FWO) at the latter stages of decomposition in the pyrolytic processes (165 kJ/mol) were higher than those in the oxidative processes (125 kJ/mol)—an indication of the distinctive phenomenon at this stage of the reaction. The Coats–Redfern kinetic model revealed that chemical reactions and diffusional models played a predominant role in the thermal decomposition process of the GG. This study showed that the thermodynamic parameters varied with the conversion ratio, and the combustion performance increased with the heating rates. The use of GG as an energy feedstock is recommended based on the findings from this work. [ABSTRACT FROM AUTHOR]

New approaches for assessing wood durability are needed to help categorize decay resistance as timber utilization shifts towards plantations or native forest regrowth that may be less durable than original native forest resources. This study evaluated attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy combined with principal component analysis (PCA) for distinguishing between groups of Alaska yellow cedar (Cupressus nootkatensis) wood for susceptibility to two decay fungi (Gloeophyllum trabeum and Rhodonia placenta) and the eastern subterranean termite (Reticulitermes flavipes). Alaska yellow cedar durability varied with test organisms, but the majority of samples were highly resistant to fungal and termite attack. Weight losses and extractives yield using sequential extractions (toluene:ethanol > ethanol > hot water) showed moderate to weak relationships. PCA analysis revealed limited ability to distinguish amongst levels of wood durability to all tested organisms. The absence of non-resistant samples may have influenced the ability of the chemometric methods to accurately categorize durability. [ABSTRACT FROM AUTHOR]

The cell wall compositional (lignin and polysaccharides) variation of two sweet sorghum varieties, Della (D) and its variant REDforGREEN (RG), was evaluated at internodes (IN) and nodes (N) using high-performance liquid chromatography (HPLC), pyrolysis-gas chromatography-mass spectrometry (Py-GCMS), X-ray diffraction (XRD), and two-dimensional (2D) 1 H- 13 C nuclear magnetic resonance (NMR). The stalks were grown in 2018 (D1 and RG1) and 2019 (D2 and RG2) seasons. In RG1, Klason lignin reductions by 16-44 and 2-26% were detected in IN and N, respectively. The analyses also revealed that lignin from the sorghum stalks was enriched in guaiacyl units and the syringyl/guaiacyl ratio was increased in RG1 and RG2, respectively, by 96% and more than 2-fold at IN and 61 and 23% at N. The glucan content was reduced by 23-27% for RG1 and by 17-22% for RG2 at internodes. Structural variations due to changes in both cellulose- and hemicellulose-based sugars were detected. The nonacylated and γ-acylated β-O-4 linkages were the main interunit linkages detected in lignin. These results indicate compositional variation of stalks due to the RG variation, and the growing season could influence their mechanical and lodging behavior.