Incorporation of postconsumer polyurethane foam into a polymer/clay aerogel matrix

The feasibility of incorporating ground recycled polyurethane (PU) foam into clay/polymer aerogels was demonstrated, and a range of compositions were prepared and characterized to determine the effect of variation in the formulations on density and mechanical properties of the resulting materials. This study followed a modified combinatorial approach. Initially, experiments were performed in water using either sodium exchanged montmorillonite or laponite clay, poly(vinyl alcohol) (PVOH) solution as the polymer binder, and the recycled PU foam. Freezing and freeze‐drying the aqueous gels produced aerogels, which were characterized through density and mechanical testing, scanning electron microscopy, and thermal gravimetric analysis. The study was expanded by exploring alternative binder chemistries, including the use of an alginate polymer in place of the PVOH or adding a polyisocyanate as a crosslinking agent for PVOH. The effect of recycled PU foam content, clay type and level, and binder type and level on the mechanical properties of the aerogels were determined and will be discussed herein. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42586.     

Effects of ultrahigh speed twin screw extrusion on the thermal and mechanical degradation of polystyrene

This article characterizes a novel twin screw extrusion (TSE) process with the capability of rotating at speeds up to 4500 rpm. The resulting extreme high shear rate is expected to result in molecular weight changes due to thermomechanical degradation of the polymeric materials being extruded, polystyrene (PS) in this case. In order to differentiate between mechanical and thermal factors affecting degradation of PS running at ultrahigh speeds and also to evaluate the relative importance of the two mechanisms, PS has been extruded at different screw speeds and different barrel temperatures with corresponding melt temperatures. Viscosity measurements and size exclusion chromatography measurements show the extent of degradation due to mechanical stress as a result of high screw rotational speeds. Furthermore, through analyzing the kinetics of PS depolymerization, the reaction rate and hypothetical apparent temperatures at each screw speed have been calculated. All results support the idea that the mechanical shear stress can be considered as the controlling factor of polymer degradation in ultrahigh speed TSE. POLYM. ENG. SCI., 56:743–751, 2016. © 2016 Society of Plastics Engineers     

Analysis of variance in capillary rheometry

The effect of deformation history (hysteresis) on transient capillary rheometric data was studied compared to conventional assumptions regarding steady state data. The factors studied were: the position instrumentation, the pressure instrumentation, entrance and exit effects, polymer melt compressibility, pressure dependence of the viscosity, and polymer melt viscous heating. Statistical analysis of variance was performed to statistically determine the sources of variance to specific degrees of confidence. The polymer melt compressibility, pressure dependence, and viscous heating were found to be statistically significant contributors of the observed variation at the 95% confidence level; the capillary length and instrumentation were not found to be significant. The results indicate that the transient behavior can vary the modeling of the apparent viscosity in a significant manner such that the model fidelity and model coefficients may vary substantially. Hence, polymer melt compressibility, pressure dependence, and viscous heating should be considered during rheological model fitting to increase model fidelity and predictive accuracy in end‐use. POLYM. ENG. SCI., 56:895–904, 2016. © 2016 Society of Plastics Engineers     

Monitoring Phenolic Composition of Maturing Maize Stover by High Performance Liquid Chromatography and Pyrolysis/Gas Chromatography/Mass Spectrometry*

Maize stovers collected every 14 days over an 84-day growth period were subjected to high-performance liquid chromatography with electrochemical detector (HPLC-ED) and pyrolysis/gas chromatography/mass spectrometry (PY/GC/MS) in order to monitor changes in the phenolic composition. Prior to HPLC-ED analyses, ground samples were sequentially extracted with (i) methanol, (ii) 0·1M sodium hydroxide and (iii) 2M sodium hydroxide in the presence of nitrobenzene to separate, respectively, free phenolic monomers, alkali-labile phenolic monomers and alkali-resistant lignin. In turn, solution (ii) was treated with alkaline nitrobenzene to obtain (iv) alkali-labile lignin. Pyrolysis was carried out on ground native samples by using a platinum heated filament pyrolyser. Increases in the absolute phenolic concentrations in the residues of 0·1M sodium hydroxide extraction and in the ratio of alkali-resistant lignin vs total lignin were observed by HPLC-ED during the first 28–42 days of maturation, reaching a steady level in the remaining maturation period. A linear increase of syringyl units vs guaiacyl units was for found the alkali-resistant lignin fraction over the entire period of maturation. Similar trends were showed by PY/GC/MS with regard to relative lignin content and syringyl/guaiacyl ratio. Both techniques showed their usefulness to gauge changes in the phenolic composition during the lignification process.     

Investigation of a Unique Commonality from a Wide Range of Natural Materials as Viewed from the Maillard Reaction Perspective

Based on the characteristics of a wide range of natural products, a more comprehensive understanding of the role of the Maillard reaction has been developed which describes a molecular basis for the production of a common set of flavourful, volatile aromatic compounds from the reactions between amino acids and sugars at elevated temperature (pressure cooking). By employing a variety of natural products, a clearer knowledge of the common mechanisms for the production of many important flavourants and odourants has been established. Regardless of the starting natural product the same qualitative profile of volatile materials is produced upon ‘pressure cooking’ an aqueous extract of the natural product. The notable differences in aroma arise not from significant differences in the qualitative nature of the materials but from variations in the quantitative distribution of the volatile materials produced.     

Genome Integrity and Neurological Disease

Neurological complications directly impact the lives of hundreds of millions of people worldwide. While the precise molecular mechanisms that underlie neuronal cell loss remain under debate, evidence indicates that the accumulation of genomic DNA damage and consequent cellular responses can promote apoptosis and neurodegenerative disease. This idea is supported by the fact that individuals who harbor pathogenic mutations in DNA damage response genes experience profound neuropathological manifestations. The review article here provides a general overview of the nervous system, the threats to DNA stability, and the mechanisms that protect genomic integrity while highlighting the connections of DNA repair defects to neurological disease. The information presented should serve as a prelude to the Special Issue “Genome Stability and Neurological Disease”, where experts discuss the role of DNA repair in preserving central nervous system function in greater depth.     

Alkane cracking reactions in zeolites with coadsorbed metal halides

HY which is loaded with SbF₅, BCl₃, or BF₃ at low coverages, one metal halide molecule per Brønsted acid site, is shown to be active in the isomerization and cracking of n-hexane and n-butane at room temperature. In contrast, NaY with the same metal halide loading shows greatly reduced activity under identical reaction conditions. The cracking reaction was repeated with DY in place of HY, demonstrating deuterium incorporation into the hexane isomer and light alkane products through interaction with the Brønsted site. Flow reactor studies demonstrate that the conversion is not constant as a function of time on stream, going through an induction period, reaching a maximum, at around 400 s, and then decaying to ~1% after 1 h.     

Do Hydropeaking Flows Alter Juvenile Fish Growth Rates? A Test with Juvenile Humpback Chub in the Colorado River

Riverine ecosystems have been altered in many large catchments by dam development to provide water, power, flood control and navigational benefits to humans. Conservation actions in these river ecosystems are commonly focused on minimum releases of water to downstream ecosystems. Increasingly minimum release approaches are being replaced with ‘experimental’ flows that mimic natural conditions in order to benefit riverine ecosystems. While these new policies are intuitive in their design, there is limited data of how riverine ecosystems actually respond to more natural flows. A test of more natural steady‐flow water release was compared with typical fluctuating hydropower flows in the adaptive management programme at Glen Canyon Dam, Arizona, during 2008–2011 to assess growth improvements of endangered juvenile humpback chub Gila cypha. Our results are counterintuitive and show that more natural steady flows reduced growth rates of juvenile humpback chub compared with fluctuating flows when both treatments occurred within the same year. Daily growth rates during steady flows of 2009 and 2010 were 0.05 and 0.07 mm day^?1 slower, respectively, than fluctuating flows those same years, despite similar water temperatures. Juvenile humpback chub also grew more slowly during steady flows that occurred in the same season. During the summer, juvenile humpback chub grew 0.12 and 0.16 mm day^?1 in fluctuating flow regimes in 2009 and 2010, respectively, and only 0.07 mm day^?1 in the experimental steady flow regime in 2011, despite higher water temperatures. Our results suggest that optimal conservation management policies for endangered species in regulated rivers may not always be achieved with more natural flows. Copyright © 2014 John Wiley & Sons, Ltd.