Policy support for cellulosic biofuels is contingent on their achieving much greater reductions in life-cycle greenhouse gas emissions than corn starch ethanol. Biomass sorghum has been suggested as a genetically and agronomically tractable feedstock species to augment near-term cellulosic feedstock production. This study used DayCent modeling to investigate biomass sorghum production emissions relative to corn with and without stover utilization at 3,265 across the rainfed United States. https://www.selleckchem.com/products/VX-770.html Sorghum produced greater average feedstock dry matter (15.6 ± 1.4 vs 14.8 ± 2.2 Mg ha-1 yr-1) and slightly lower estimated ethanol energy yields (10.6 ± 1.0 vs 11.8 ± 2.9 MJ m-2 yr-1) as corn grain with 75% stover collection. The high biomass removals in both the sorghum and corn stover scenarios led to soil organic carbon losses on 90 and 100% of sites, respectively. Average feedstock production emissions intensities were similar between sorghum and corn with 75% stover removal (17.6 ± 2.8 vs 18.8 ± 3.0 g CO2e MJ-1), but were notably lower under sorghum for sites in the southwestern study region (13.6 ± 3.0 vs 22.5 ± 3.1 g CO2e MJ-1). These results suggest that biomass sorghum produces cellulosic feedstock with similar emissions to corn grain and at current yield levels is unlikely to meet the Renewable Fuel Standard emissions reduction threshold for cellulosic biofuels.Low-field proton nuclear magnetic resonance (LF-1H NMR) devices based on permanent magnets are a promising analytical tool to be extensively applied to the process analytical chemistry scenario. To enhance its analytical applicability in samples where the spectral resolution is compromised, multivariate regression methods are required. However, building a robust calibration model, such as partial least squares (PLS) regression, is a laborious task because (1) the number of measurements required during the calibration process is large and (2) the procedure must be repeated when the instrument is changed or after a certain period due to the long-term stability of the instrument. Thus, the present work describes the application of calibration transfer methodologies (direct standardization (DS), piece-wise direct standardization (PDS), and double-window piece-wise direct standardization (DWPDS)) on LF-1H NMR to exempt the necessity of a recalibration procedure when moving from the original spectrometer to a second one with the same, lower, or higher magnetic field. These calibration transfer methodologies were tested with PLS models built on a 60 MHz (for the proton Larmor frequency) spectrometer to predict the specific gravity (SG), distillation temperature (T50%), and final boiling point (FBP) of commercial gasoline. The results showed that the DWPDS method applying only 2 to 7 transference samples enables the transference of all PLS models built on the primary instrument (60 MHz) to other (43, 60, and 80 MHz) different instruments, reaching the same RMSEP values as the primary instrument 1.2 kg/m3 for SG, 5.1 °C for FBP, and 1.1 °C for T50%.We investigated polydimethylsiloxane/poly(methyl methacrylate) (PDMS/PMMA) interpenetrating polymer networks (IPNs) by both sequential and simultaneous syntheses. In the sequential IPN, the PDMS network was first thermally cured after which methyl methacrylate was swelled in and UV photopolymerized in situ. The simultaneous IPN consists of a one-pot, single-step UV cure of both components. Pure shear fracture and tensile tests were used to extract the Young's modulus, critical fracture strain, and fracture energy of the materials at varying PMMA fractions (up to 50 wt %). At high PMMA fractions, a maximum increase in Young's modulus (42×) and fracture energy (21×) was observed with little sacrifice in the optical properties and the extensibility of notched samples. The Krieger-Dougherty model for particle reinforcement was fit to the modulus data as a function of the PMMA fraction and showed good agreement. The optical properties and microstructure of the IPNs were investigated by UV-visible light transmission, small-angle X-ray scattering (SAXS), and atomic force microscopy (AFM). As the weight fraction of PMMA increased, the simultaneous IPN became less transparent, while the sequential material showed the opposite trend. In the sequential IPN, the minority phase size decreased with increasing PMMA fraction, while it was constant for the simultaneous IPN. Therefore, it was concluded that the sequential IPN transparency is controlled by the size of the PMMA domains, but the simultaneous IPN transparency is controlled by the PMMA fraction. SAXS and AFM also showed evidence of bicontinuous network formation in the simultaneous IPN, which may affect the optical and mechanical properties.Anomaly detection (AD) in high-volume environmental data requires one to tackle a series of challenges associated with the typical low frequency of anomalous events, the broad-range of possible anomaly types, and local nonstationary environmental conditions, suggesting the need for flexible statistical methods that are able to cope with unbalanced high-volume data problems. Here, we aimed to detect anomalies caused by technical errors in water-quality (turbidity and conductivity) data collected by automated in situ sensors deployed in contrasting riverine and estuarine environments. We first applied a range of artificial neural networks that differed in both learning method and hyperparameter values, then calibrated models using a Bayesian multiobjective optimization procedure, and selected and evaluated the "best" model for each water-quality variable, environment, and anomaly type. We found that semi-supervised classification was better able to detect sudden spikes, sudden shifts, and small sudden spikes, whereas supervised classification had higher accuracy for predicting long-term anomalies associated with drifts and periods of otherwise unexplained high variability.Three-dimensional bioprinting uses additive manufacturing techniques for the automated fabrication of hierarchically organized living constructs. The building blocks are often hydrogel-based bioinks, which need to be printed into structures with high shape fidelity to the intended computer-aided design. For optimal cell performance, relatively soft and printable inks are preferred, although these undergo significant deformation during the printing process, which may impair shape fidelity. While the concept of good or poor printability seems rather intuitive, its quantitative definition lacks consensus and depends on multiple rheological and chemical parameters of the ink. This review discusses qualitative and quantitative methodologies to evaluate printability of bioinks for extrusion- and lithography-based bioprinting. The physicochemical parameters influencing shape fidelity are discussed, together with their importance in establishing new models, predictive tools and printing methods that are deemed instrumental for the design of next-generation bioinks, and for reproducible comparison of their structural performance.