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The presence of water greatly influences time-dependent rock deformation. An understanding of how water can affect the time-dependent mechanical behavior of rock is important when assessing the long-term stability of geotechnical projects. While the previous studies have performed brittle creep experiments on oven-dry or fully-saturated rocks, we report here on a study designed to better understand brittle creep at different levels of saturation. We performed brittle creep experiments on oven-dry samples of red sandstone (Hunan province, China) and samples of the sandstone pre-immersed in water for different durations (from 2 to 8 days). These samples were deformed at a constant stress in one of either two conditions: dry or submerged in water. Before performing creep experiments, we first performed a series of water absorption and constant stress rate experiments to guide the stresses required for our creep tests and to assist with their interpretation. Our creep experiments show that immersion in water greatly increased the minimum creep strain rate and greatly shortened the time-to-failure when compared to the dry state. In detail, the minimum creep strain rate and time-to-failure increased and decreased, respectively, as pre-immersion duration increased from 4 to 6 days, but did not change as the duration was further increased to 8 days. We attribute this to the saturation of microcracks between 4 and 6 days (i.e., water imbibition was complete, or close to completion, following 6 days). We also show that oven-dry samples deformed at a constant stress underwater fail at stresses much lower than oven-dry samples deformed under dry conditions, due to the imbibition of water during deformation. Samples pre-immersed in water, but deformed in the dry condition were characterized by lower strain rates and longer time-to-failure than those pre-immersed in water and deformed underwater. Our explanation for this is that, due to the availability of water, crack tips can remain hydrated when the sample is deformed underwater, thus increasing the efficacy of stress corrosion cracking. The relationships and data provided herein inform on the long-term stability of engineering structures.

In this article, some necessary and sufficient conditions are shown for weighted weak type mixed Φ -inequality and weighted extra-weak type mixed Φ -inequality for martingale maximal operator. The obtained results generalize some existing statements.

The development of high-performance ultraelastic metals with superb strength, a large elastic strain limit and temperature-insensitive elastic modulus (Elinvar effect) are important for various industrial applications, from actuators and medical devices to high-precision instruments 1 , 2 . The elastic strain limit of bulk crystalline metals is usually less than 1 per cent, owing to dislocation easy gliding. Shape memory alloys 3 —including gum metals 4 , 5 and strain glass alloys 6 , 7 —may attain an elastic strain limit up to several per cent, although this is the result of pseudo-elasticity and is accompanied by large energy dissipation 3 . Recently, chemically complex alloys, such as ‘high-entropy’ alloys 8 , have attracted tremendous research interest owing to their promising properties 9 – 15 . In this work we report on a chemically complex alloy with a large atomic size misfit usually unaffordable in conventional alloys. The alloy exhibits a high elastic strain limit (approximately 2 per cent) and a very low internal friction (less than 2 × 10 −4 ) at room temperature. More interestingly, this alloy exhibits an extraordinary Elinvar effect, maintaining near-constant elastic modulus between room temperature and 627 degrees Celsius (900 kelvin), which is, to our knowledge, unmatched by the existing alloys hitherto reported. A chemically complex alloy that exhibits a high elastic strain limit and low internal friction is described; it also has an Elinvar effect (invariant elastic modulus) over a large temperature range, up to 627 °C.

Sepsis is a prevalent health issue that can lead to central nervous system (CNS) inflammation with long-term behavioral and cognitive alterations. Using unbiased proteomic profiling of over 100 different cytokines, we found that Lipocalin-2 (LCN2) was the most substantially elevated protein in the CNS after peripheral administration of lipopolysaccharide (LPS). To determine whether the high level of LCN2 in the CNS is protective or deleterious, we challenged Lcn2-/- mice with peripheral LPS and determined effects on behavior and neuroinflammation. At a time corresponding to peak LCN2 induction in wild-type (WT) mice injected with LPS, Lcn2-/- mice challenged with LPS had exacerbated levels of pro-inflammatory cytokines and exhibited significantly worsened behavioral phenotypes. To determine the extent of global inflammatory changes dependent upon LCN2, we performed an RNAseq transcriptomic analysis. Compared with WT mice injected with LPS, Lcn2-/- mice injected with LPS had unique transcriptional profiles and significantly elevated levels of multiple pro-inflammatory molecules. Several LCN2-dependent pathways were revealed with this analysis including, cytokine and chemokine signaling, nucleotide-binding oligomerization domain-like receptor signaling and Janus kinase-signal transducer and activator of transcription signaling. These findings demonstrate that LCN2 serves as a potent protective factor in the CNS in response to systemic inflammation and may be a potential candidate for limiting sepsis-related CNS sequelae.

Our understanding of when and how humans adapted to living on the Tibetan Plateau at altitudes above 2000 to 3000 meters has been constrained by a paucity of archaeological data. Here we report data sets from the northeastern Tibetan Plateau indicating that the first villages were established only by 5200 calendar years before the present (cal yr B.P.). Using these data, we tested the hypothesis that a novel agropastoral economy facilitated year-round living at higher altitudes since 3600 cal yr B.P. This successful subsistence strategy facilitated the adaptation of farmers-herders to the challenges of global temperature decline during the late Holocene.

An anomaly in differential scanning calorimetry has been reported in a number of metallic glass materials in which a broad exothermal peak was observed between the glass and crystallization temperatures. The mystery surrounding this calorimetric anomaly is epitomized by four decades long studies of Pd-Ni-P metallic glasses, arguably the best glass-forming alloys. Here we show, using a suite of in situ experimental techniques, that Pd-Ni-P alloys have a hidden amorphous phase in the supercooled liquid region. The anomalous exothermal peak is the consequence of a polyamorphous phase transition between two supercooled liquids, involving a change in the packing of atomic clusters over medium-range length scales as large as 18 Å. With further temperature increase, the alloy reenters the supercooled liquid phase, which forms the room-temperature glass phase on quenching. The outcome of this study raises a possibility to manipulate the structure and hence the stability of metallic glasses through heat treatment. An anomalous exothermal calorimetric peak far below crystallization temperatures in prototypical Pd-Ni-P glasses has been recognized for four decades. Here authors use neutron and high-energy X-ray diffraction to find evidence for a polyamorphous phase transition where medium-range order undergoes large changes while short-range order changes little.

A rechargeable lithium anode requires a porous structure for a high capacity, and a stable electrode/electrolyte interface against dendrite formation and polysulfide crossover when used in a lithium-sulfur battery. Here, we design two simple steps of spontaneous reactions for protecting porous lithium electrodes. First, a reaction between molten lithium and sulfur-impregnated carbon nanofiber forms a fibrous network with a lithium shell and a carbon core. Second, we coat the surface of this porous lithium electrode with a composite of lithium bismuth alloys and lithium fluoride through another spontaneous reaction between lithium and bismuth trifluoride, solvated with phosphorous pentasulfide, which also polymerizes with lithium sulfide residual in the electrode to form a solid electrolyte layer. This protected porous lithium electrode enables stable operation of a lithium-sulfur battery with a sulfur loading of 10.2 mg cm −2 at 6.0 mA cm −2 for 200 cycles. Stabilizing lithium anodes has been a crucial yet challenging task in developing high-energy batteries. Here the authors design two simple steps of spontaneous reactions to achieve a porous lithium electrode with a composite protective layer, enabling high-loading Li-S batteries with excellent cyclability.

The phenomena of antisymmetric magnetoresistance and the planar Hall effect are deeply entwined with ferromagnetism. The intrinsic magnetization of the ordered state permits these unusual and rarely observed manifestations of Onsager’s theorem when time reversal symmetry is broken at zero applied field. Here we study two classes of ferromagnetic materials, rare-earth magnets with high intrinsic coercivity and antiferromagnetic pyrochlores with strongly-pinned ferromagnetic domain walls, which both exhibit antisymmetric magnetoresistive behavior. By mapping out the peculiar angular variation of the antisymmetric galvanomagnetic response with respect to the relative alignments of the magnetization, magnetic field, and electrical current, we experimentally distinguish two distinct underlying microscopic mechanisms: namely, spin-dependent scattering of a Zeeman-shifted Fermi surface and anomalous electron velocities. Our work demonstrates that the anomalous electron velocity physics typically associated with the anomalous Hall effect is prevalent beyond the ρ xy ( H z ) channel, and should be understood as a part of the general galvanomagnetic behavior. Magnetoresitance (MR) is a tool to study electronic transport and spin order in metals. Here, the authors demonstrate two different microscopic origins of antisymmetric linear MR from both Zeeman-split Fermi surface and anomalous electron velocity.

Bioavailability is an eternal topic that cannot be circumvented by peroral drug delivery. Adequate blood drug exposure after oral administration is a prerequisite for effective treatment. Nanovesicles as pleiotropic oral vehicles can solubilize, encapsulate, stabilize an active ingredient and promote the payload absorption via various mechanisms. Vesicular systems with nanoscale size, such as liposomes, niosomes and polymersomes, provide a versatile platform for oral delivery of drugs with distinct nature. The amphiphilicity of vesicles in structure allows hydrophilic and lipophilic molecule(s) either or both to be loaded, being encapsulated in the aqueous cavity or the inner core, respectively. Depending on high oral transport efficiency based on their structural flexibility, gastrointestinal stability, biocompatibility, and/or intestinal epithelial affinity, nanovesicles can markedly augment the oral bioavailability of various poorly absorbed drugs. Vesicular drug delivery systems (VDDSs) demonstrate a lot of preferences and are becoming more prominent of late years in biomedical applications. Equally, these systems can potentiate a drug's therapeutic index by ameliorating the oral absorption. This review devotes to comment on various VDDSs with special emphasis on the peroral drug delivery. The classification of nanovesicles, preparative processes, intestinal transport mechanisms, in vivo fate, and design rationale were expounded. Knowledge on vesicles-mediated oral drug delivery for bioavailability enhancement has been properly provided. It can be concluded that VDDSs with many merits will step into an energetic arena in oral drug delivery. Keywords: vesicles, oral drug delivery, bioavailability, liposomes, niosomes, exosomes

This study introduces a hybrid battery thermal management system (BTMS) that incorporates coolant plates with four-leaf clover microchannels, along with fins that serve as thermal bridges between the phase change material (PCM) and the coolant, with the aim of enhancing the overall performance of the BTMS by improving cooling quality. Initially, the accuracy of the single-cell heat-generation model was experimentally validated. Subsequently, computational fluid dynamics (CFD) simulations were employed to analyze the effects of channel width, quantity, coolant flow velocity, and initial coolant temperature on the thermal behavior of the hybrid BTMS. The findings indicate that, while channel quantity has a minor impact on system performance, increasing the channel width from 1 mm to 2.5 mm at a flow velocity of 0.125 m/s can enhance the cooling capacity of the hybrid model. Additionally, adjusting the initial coolant temperature can enhance the temperature uniformity of the battery pack. Under the optimal configuration, the battery pack reaches a maximum temperature of 37.12 °C with a 3.71 °C intra-pack difference. The PCM liquid fraction is 53.98 % lower, and the peak temperature is 5.09 °C lower than that with pure PCM cooling. Compared with the conventional parallel-channel design, the biomimetic design reduces the pressure drop by 32.93 Pa. Compared with the spider-web-channel design, the temperature of the liquid-cooled plate can be reduced by 2.97 °C.