Effects of Mixture and Aggregate Type on Over-Compaction in Hot Mix Asphalt in Tennessee

Correct compaction is vital for asphalt mixture service life. An adequately compacted mixture with inferior properties can achieve better performance than a mixture with excellent properties but poorly compacted. This study investigated resistance to damage caused by over-compaction by utilizing the locking point concept. Over-compaction might cause damage to the aggregate structure and decrease service life. The locking point is defined as the moment during mixture compaction at which an aggregate skeleton is developed and becomes stable. Beyond the locking point, more compaction energy does not significantly increase mixture density and can damage aggregate particles. A total of 15 mixtures was utilized and evaluated using the gyratory compactor. Among them, five dense-graded plant mixtures contained different aggregates and binders, and 10 laboratory mixtures (three types: the surface, the base, and stone mastic asphalt [SMA]) were designed with the most popular coarse aggregates in Tennessee: hard limestone, soft limestone, gravel, and granite. The results of this study show that the highest locking point was reached by the mixtures containing gravel. The SMA mixtures have, on average, lower locking points than the dense-graded mixtures. Most of the dense-graded mixtures made with crushed stones failed in the range of +20 to +30 gyrations, whereas the samples made with gravels failed in the range of +30 to +40 gyrations, indicating that gravel seems to be the most resistant to damage.

Conversion of alpine pastureland to artificial grassland altered CO2 and N2O emissions by decreasing C and N in different soil aggregates

Background The impacts of land use on greenhouse gases (GHGs) emissions have been extensively studied. However, the underlying mechanisms on how soil aggregate structure, soil organic carbon (SOC) and total N (TN) distributions in different soil aggregate sizes influencing carbon dioxide (CO2), and nitrous oxide (N2O) emissions from alpine grassland ecosystems remain largely unexplored. Methods A microcosm experiment was conducted to investigate the effect of land use change on CO2and N2O emissions from different soil aggregate fractions. Soil samples were collected from three land use types, i.e., non-grazing natural grassland (CK), grazing grassland (GG), and artificial grassland (GC) in the Bayinbuluk alpine pastureland. Soil aggregate fractionation was performed using a wet-sieving method. The variations of soil aggregate structure, SOC, and TN in different soil aggregates were measured. The fluxes of CO2 and N2O were measured by a gas chromatograph. Results Compared to CK and GG, GC treatment significantly decreased SOC (by 24.9–45.2%) and TN (by 20.6–41.6%) across all soil aggregate sizes, and altered their distributions among soil aggregate fractions. The cumulative emissions of CO2 and N2O in soil aggregate fractions in the treatments of CK and GG were 39.5–76.1% and 92.7–96.7% higher than in the GC treatment, respectively. Moreover, cumulative CO2emissions from different soil aggregate sizes in the treatments of CK and GG followed the order of small macroaggregates (2–0.25 mm) > large macroaggregates (> 2 mm) > micro aggregates (0.25–0.053 mm) > clay +silt (< 0.053 mm), whereas it decreased with aggregate sizes decreasing in the GC treatment. Additionally, soil CO2 emissions were positively correlated with SOC and TN contents. The highest cumulative N2O emission occurred in micro aggregates under the treatments of CK and GG, and N2O emissions among different aggregate sizes almost no significant difference under the GC treatment. Conclusions Conversion of natural grassland to artificial grassland changed the pattern of CO2 emissions from different soil aggregate fractions by deteriorating soil aggregate structure and altering soil SOC and TN distributions. Our findings will be helpful to develop a pragmatic management strategy for mitigating GHGs emissions from alpine grassland.

The Cryo-EM Effect: Structural Biology of Neurodegenerative Disease Aggregates

Neurogenerative diseases are characterized by diverse protein aggregates with a variety of microscopic morphologic features. Although ultrastructural studies of human neurodegenerative disease tissues have been conducted since the 1960s, only recently have near-atomic resolution structures of neurodegenerative disease aggregates been described. Solid-state nuclear magnetic resonance spectroscopy and X-ray crystallography have provided near-atomic resolution information about in vitro aggregates but pose logistical challenges to resolving the structure of aggregates derived from human tissues. Recent advances in cryo-electron microscopy (cryo-EM) have provided the means for near-atomic resolution structures of tau, amyloid-β (Aβ), α-synuclein (α-syn), and transactive response element DNA-binding protein of 43 kDa (TDP-43) aggregates from a variety of diseases. Importantly, in vitro aggregate structures do not recapitulate ex vivo aggregate structures. Ex vivo tau aggregate structures indicate individual tauopathies have a consistent aggregate structure unique from other tauopathies. α-syn structures show that even within a disease, aggregate heterogeneity may correlate to disease course. Ex vivo structures have also provided insight into how posttranslational modifications may relate to aggregate structure. Though there is less cryo-EM data for human tissue-derived TDP-43 and Aβ, initial structural studies provide a basis for future endeavors. This review highlights structural variations across neurodegenerative diseases and reveals fundamental differences between experimental systems and human tissue derived protein inclusions.

Enhancement of Polymer Structural Ordering in Polymer-Stabilised Blue Phases for Improved Electro-Optical Properties

Polymer-stabilised blue phase (PSBP) could be employed in novel fast response optical and photonic devices. It is inferred that inside PSBPs, the polymers are selectively aggregated by location in −1/2 disclinations, which are defects coexisting with the blue phase as a periodic lattice, thereby extending the temperature range of the blue phase. The polymer aggregate structure in PSBPs strongly affects their physical properties. In this study, we employed a non-destructive synchrotron ultra-small-angle X-ray diffraction analysis to investigate the effect of polymerisation rates on the polymer aggregate structure in PSBPs prepared with monomers of different polymerisation rates and examined the structure formation process of the polymer during polymerisation. When methacrylate monomers, which exhibit a relatively low polymerisation rate, were used to form polymers in PSBP, the resulting polymer was more selectively aggregated at disclinations in the PSBP. Furthermore, the electro-optical effect in the PSBP was successfully improved by reducing the polymer concentration in the PSBPs prepared with the optimised monomer combinations.