Improving a Mg/S Battery with YCl 3 Additive and Magnesium Polysulfide
Not Available
25 ENERGY STORAGE↗
Engineering topics
Xu, Yan
Publications and source records attributed to Xu, Yan.
Improving a Mg/S Battery with YCl 3 Additive and Magnesium Polysulfide
In the originally published version of this article, the SEM image in Figure 4B inadvertently features the wrong sample. The correct Figure 4B is shown below. The authors declare that this correction does not affect the description, interpretation, or the original conclusions of the manuscript. The authors regret the inconvenience this error may have caused.
25 ENERGY STORAGE↗
Dynamic recrystallization kinetics and microstructure evolution of an AZ91D magnesium alloy during hot compression
Highlights: • DRX kinetic model is developed for the aged AZ91D magnesium alloy. • The DRX behavior in different strained regions was investigated. • Four morphologies of the second phase were proposed during the hot compression tests. • The nucleation mechanisms of the DRX grains were clarified. - Abstract: The flow behavior of as-cast AZ91D magnesium alloy was evaluated by isothermal compression tests within the temperatures of 220 °C, 260 °C, 300 °C, 340 °C, and 380 °C, and the strain rates of 0.001, 0.01, 0.1, 1 and 10s{sup −1}. Based on the stress-strain curve and hyperbolic sine function, the thermal activation energy and the strain rate sensitivity of the material were determined to be 142.2726 kJ·mol{sup −1} and 0.142, respectively. The S type evolution of the dynamic recrystallization with the increasing strain that dynamic recrystallization (DRX) model obtained from stress and strain data. There was a good consistency between the proposed DRX kinetics model and microstructure observation results. Combining isothermal compression specimens with finite element and scanning electron microscopy (SEM) analysis indicated that the sample can be divided into rarely recrystallized region, partially recrystallized region and completely recrystallized region, which falls within the dense deformation zone, free deformation zone and severe deformation zone, respectively. The different forms of the β-Mg{sub 17}Al{sub 12} phase induced by compression tests were confirmed by SEM. Nucleation mechanisms of the DRX were discussed with reference to the transmission electron microscope (TEM) analysis results.
36 MATERIALS SCIENCE↗
Spatial distribution of marker gene activity in the mouse lung during alveolarization
Here, this data is a curated collection of visual images of gene expression patterns from the pre- and post-natal mouse lung, accompanied by associated mRNA probe sequences and RNA-Seq expression profiles. Mammalian lungs undergo significant growth and cellular differentiation before and after the transition to breathing air. Documenting normal lung development is an important step in understanding abnormal lung development, as well as the challenges faced during a preterm birth. Images in this dataset indicate the spatial distribution of mRNA transcripts for over 500 different genes that are active during lung development, as initially determined via RNA-Seq. Images were systematically acquired using high-throughput in situ hybridization with non-radioactive digoxigenin-labeled mRNA probes across mouse lungs from developmental time points E16.5, E18.5, P7, and P28.
59 BASIC BIOLOGICAL SCIENCES↗
Coronal Hard X-Ray Sources Revisited
This paper reports on the re-analysis of solar flares in which the hard X-rays (HXRs) come predominantly from the corona rather than from the more usual chromospheric footpoints. All of the 26 previously analyzed event time intervals, over 13 flares, are re-examined for consistency with a flare model in which electrons are accelerated near the top of a magnetic loop which has a sufficiently high density to stop most of the electrons by Coulomb collisions before they can reach the footpoints. Of particular importance in the previous analysis was the finding that the length of the coronal HXR source increased with energy in the 20–30 keV range. However, after allowing for the possibility that footpoint emission at the higher energies affects the inferred length of the coronal HXR source, and using analysis techniques that suppress the possible influence of such footpoint emission, we conclude that there is no longer evidence that the length of the HXR coronal sources increase with increasing energy. In fact, for the six flares and 12 time intervals that satisfied our selection criteria, the loop lengths decreased on average by 1.0 ± 0.2 arcsec between 20 and 30 keV, with a standard deviation of 3.5 arcsec. We find strong evidence that the peak of the coronal HXR source increases in altitude with increasing energy. For the thermal component of the emission, this is consistent with the standard CHSKP flare model in which magnetic reconnection in a coronal current sheet results in new hot loops being formed at progressively higher altitudes. The explanation for the nonthermal emission is not so clear.
Gamma rays↗
Lithium nitrate: A double-edged sword in the rechargeable lithium-sulfur cell
Lithium nitrate (LiNO 3 ) has been the most studied electrolyte additive in lithium-sulfur (Li-S) cells, due to its known function of suppressing the shuttle effect in Li-S cells, which provides a significant increase in the cell's coulombic efficiency and cycling stability. Previous studies indicated that LiNO 3 participated in the formation of a passive layer on the lithium electrode and thus suppressed the redox shuttle of the dissolved polysulfides. However, the effects of the LiNO 3 on the positive electrode materials have rarely been investigated. By combining scanning electron microscopy, element-selective X-ray absorption spectroscopy, and electrochemical characterizations, we performed a comprehensive study of how the LiNO 3 altered the properties of the sulfur electrode/electrolyte interface in Li-S cells and thus influenced the cell performance. We found that LiNO 3 is a double-edged sword in the Li-S cell: on one hand, it increased the consumption of the active sulfur; on the other hand, it promoted the survival of the carbon matrix constituent in the sulfur electrode. These two competitive effects indicated that a proper moderate concentration of LiNO 3 is required to achieve an optimized cell performance.
25 ENERGY STORAGE↗
Structural basis of neurosteroid anesthetic action on GABAA receptors
Type A γ-aminobutyric acid receptors (GABA A Rs) are inhibitory pentameric ligand-gated ion channels in the brain. Many anesthetics and neurosteroids act through binding to the GABA A R transmembrane domain (TMD), but the structural basis of their actions is not well understood and no resting-state GABA A R structure has been determined. Here, we report crystal structures of apo and the neurosteroid anesthetic alphaxalone-bound desensitized chimeric α1GABA A R (ELIC-α1GABA A R). The chimera retains the functional and pharmacological properties of GABA A Rs, including potentiation, activation and desensitization by alphaxalone. The apo-state structure reveals an unconventional activation gate at the intracellular end of the pore. The desensitized structure illustrates molecular determinants for alphaxalone binding to an inter-subunit TMD site. These structures suggest a plausible signaling pathway from alphaxalone binding at the bottom of the TMD to the channel gate in the pore-lining TM2 through the TM1–TM2 linker. The study provides a framework to discover new GABA A R modulators with therapeutic potential.
59 BASIC BIOLOGICAL SCIENCES↗
Cell type-resolved human lung lipidome reveals cellular cooperation in lung function
Cell type-resolved proteome analyses of the brain, heart and liver have been reported, however a similar effort on the lipidome is currently lacking. Here we applied liquid chromatography-tandem mass spectrometry to characterize the lipidome of major lung cell types isolated from human donors, representing the first lipidome map of any organ. We coupled this with cell type-resolved proteomics of the same samples (available at Lungmap.net). Complementary proteomics analyses substantiated the functional identity of the isolated cells. Lipidomics analyses showed significant variations in the lipidome across major human lung cell types, with differences most evident at the subclass and intra-subclass (i.e. total carbon length of the fatty acid chains) level. Further, lipidomic signatures revealed an overarching posture of high cellular cooperation within the human lung to support critical functions. Our complementary cell type-resolved lipid and protein datasets serve as a rich resource for analyses of human lung function.
Kyle, Jennifer E.↗
B2 Grain Growth Behavior of a Ti-22Al-25Nb Alloy Fabricated by Hot Pressing Sintering
Grain growth behavior of a powder metallurgy (P/M) Ti-22Al-25Nb alloy was investigated by applying a series of isothermal treatment tests over a wide range of temperatures and holding times. An isothermal treatment scheme was conducted in the B2 phase region (1070-1110 °C) and α{sub 2} + B2 phase region (1010-1050 °C) at holding times of 10, 30 min, 1, 2, and 3 h, respectively. The effects of temperature and holding time on the microstructure evolution and microhardness of the P/M Ti-22Al-25Nb alloy at elevated temperatures were evaluated using optical microscope, scanning electron microscope, x-ray diffraction, and Vickers hardness test techniques. The results revealed that the alloy’s treated microstructure was closely linked to temperature and holding time, respectively. The change law of B2 grain growth with holding time and temperature can be well interpreted by the Beck equation and Hillert equation, respectively. The B2 grain growth exponent n and activation energy Q were acquired based on experimental data in the α{sub 2} + B2 and B2 phase regions. In addition, the grain growth contour map for the P/M Ti-22Al-25Nb alloy was constructed to depict variations in B2 grain size based on holding time and temperature.
36 MATERIALS SCIENCE↗
Exosomal proteome analysis of human plasma to monitor sepsis progression
Highlights: • As low as 300 μL human plasma is sufficient for exosome isolation using our one-step density gradient ultracentrifugation. • Protein profiling of septic plasma exosomes are closely related to immune responses. • SPTLC3 may play important roles in development of sepsis. Exosomes are cell-derived vesicles containing RNA, lipid, and protein, which act in body immune response, intercellular signaling and some other important biological processes. Exosomes have been extensively studied in the past several years on their disease related mechanisms and potential roles to monitor disease progression as biomarkers. Compared with analyzing exosome RNA, comprehensive proteome profiling of exosomes in clinical samples (e.g. blood) are highly demanded but limited mainly due to lack of a reproducible method for efficient exosome extraction. In this study, we evaluated and optimized an exosome preparation approach using one-step ultracentrifugation through an Optiprep™ cushion. Exosomes prepared via this method and analyzed by mass spectrometry using Q-Exactive plus, has led to reproducible identification and quantification of 200 + proteins from human plasma samples of as little as 300 μL. Therefore, such a straightforward exosome extract method has enable us to deeply profile exosome proteomes from human blood at a scale of clinical studies. As a proof of principal, we practiced this approach in analyzing the exosome proteomic profiles of blood samples collected from a sepsis patient during six time points after diagnosis. Among the 238 proteins identified and quantified across the 6 samples, protein SPTLC3 involved in the sphingolipid metabolism, shows a negative correlation (p = 0.02, correlation coefficient = −0.984) with disease progression indicated by body temperature (BD) and C-reactive protein (CRP). Therefore, SPTLC3 could be an interesting target for future study on molecular mechanism of sepsis development, as well as potential classifier to monitor clinical progression of sepsis.
60 APPLIED LIFE SCIENCES↗
Global status of recycling waste solar panels: A review
Highlights: • Solar panel recycling minimizes waste of environmental and economic resources. • Several processing methods from the literature are evaluated. • The status of the management for waste solar panels are systemically reviewed and discussed. • Policy should be formulated to encourage recycling of waste solar panels. • Manufacturers should take greater responsibility for recycling. - Abstract: With the enormous growth in the development and utilization of solar-energy resources, the proliferation of waste solar panels has become problematic. While current research into solar panels has focused on how to improve the efficiency of the production capacity, the dismantling and recycling of end-of-life (EOL) panels are seldom considered, as can be seen, for instance, in the lack of dedicated solar-panel recycling plants. EOL solar-panel recycling can effectively save natural resources and reduce the cost of production. To address the environmental conservation and resource recycling issues posed by the huge amount of waste solar panels regarding environmental conservation and resource recycling, the status of the management and recycling technologies for waste solar panels are systemically reviewed and discussed in this article. This review can provide a quantitative basis to support the recycling of PV panels, and suggests future directions for public policy makers. At present, from the technical aspect, the research on solar panel recovery is facing many problems, and we need to further develop an economically feasible and non-toxic technology. The research on solar photovoltaic panels’ management at the end of life is just beginning in many countries, and there is a need for further improvement and expansion of producer responsibility.
14 SOLAR ENERGY↗
Production of Curdlan Grown on Cassava Starch Waste Hydrolysates
Cassava starch waste hydrolysates (CSWHs) with different degrees of polymerisation, i.e., CSWHs-1, CSWHs-2 and CSWHs-3, were prepared through the hydrolysis of cassava starch waste with thermostable a-amylase from Thermococcus sp. HJ21. The prepared CSWHs were then used as a carbon source for curdlan production with Alcaligenes faecalis ATCC 31749. The amount of curdlan produced and the glucosyltransferase activity during curdlan synthesis increased more obviously when CSWHs-2 was used as the carbon source than when glucose was used. Using both carbon sources, the maximum curdlan production was observed at day 5, and the maximum glucosyltransferase activity was observed at day 4. Glucosyltransferase activity decreased thereafter, and biomass continued to increase until the end of the experiment (day 6). Results indicated that the enhanced curdlan production with CSWHs as the carbon source was highly correlated with glucosyltransferase activity.
09 BIOMASS FUELS↗
Hydrogenation of Diesters on Copper Catalyst Anchored on Ordered Hierarchical Porous Silica: Pore size effect
An ordered hierarchically porous silica (HPS) with the coexistence of both mesopores and abundant micropores was fabricated and used as support for the preparation of copper-based catalysts (Cu/HPS). The ordered mesoporous structure of the Cu/HPS catalysts was retained. In addition, both Cu0 and Cu+ species are found to be highly dispersed. It might be attributed to the anchoring effect of micropores and the formation of Cu-O-Si species derived from the strong interaction between surface silica and copper precursor. The Cu/HPS catalysts showed excellent performances in the hydrogenation of dimethyl adipate. The catalytic activity in dimethyl oxalate hydrogenation depended on the surface reaction, while the activity in dimethyl adipate hydrogenation will be readily controlled by pore diffusion, which can be improved by tailoring the pore size of HPS. These findings could be meaningful instruction for the rational design of industrial catalysts for the hydrogenation of various diesters.
ester, hydrogenation, higherarchical, copper, diff↗
Alveolar injury and regeneration following deletion of ABCA3
Adaptation to air breathing after birth is dependent upon the synthesis and secretion of pulmonary surfactant by alveolar type 2 (AT2) cells. Surfactant, a complex mixture of phospholipids and proteins, is secreted into the alveolus, where it reduces collapsing forces at the air-liquid interface to maintain lung volumes during the ventilatory cycle. ABCA3, an ATP-dependent Walker domain containing transport protein, is required for surfactant synthesis and lung function at birth. Mutations in ABCA3 cause severe surfactant deficiency and respiratory failure in newborn infants. We conditionally deleted the Abca3 gene in AT2 cells in the mature mouse lung. Loss of ABCA3 caused alveolar cell injury and respiratory failure. ABCA3-related lung dysfunction was associated with surfactant deficiency, inflammation, and alveolar-capillary leak. Extensive but incomplete deletion of ABCA3 caused alveolar injury and inflammation, and it initiated proliferation of progenitor cells, restoring ABCA3 expression, lung structure, and function. M2-like macrophages were recruited to sites of AT2 cell proliferation during the regenerative process and were present in lung tissue from patients with severe lung disease caused by mutations in ABCA3. The remarkable and selective regeneration of ABCA3-sufficient AT2 progenitor cells provides plausible approaches for future correction of ABCA3 and other genetic disorders associated with surfactant deficiency and acute interstitial lung disease.
Rindler, Tara N.↗
EMC3 coordinates surfactant protein and lipid homeostasis required for respiration
Adaptation to respiration at birth is dependent upon the synthesis of pulmonary surfactant, a lipid-protein complex that reduces surface tension at the air-liquid interface in the alveoli, preventing lung collapse during the ventilatory cycle. Herein, we demonstrate that Emc3/Tmem111, the gene encoding a subunit of endoplasmic reticulum membrane complex, was required for pulmonary surfactant synthesis and lung function at birth. Conditional deletion of Emc3 in embryonic lung epithelial cells disrupted the synthesis and packaging of surfactant lipids and proteins, impaired the formation of lamellar bodies and induced the unfolded protein response in alveolar type 2 (AT2) cells. EMC3 was essential for the processing and routing of surfactant proteins, SP-B and SP-C, and the biogenesis of the phospholipid transport protein ABCA3. Transcriptomic, lipidomic, and proteomic analyses demonstrated that EMC3 coordinates the assembly of lipids and proteins in AT2 cells that are necessary for surfactant synthesis and function at birth.
Tang, Xiaofang↗
High-quality genome sequence of the radioresistant bacterium Deinococcus ficus KS 0460
Abstract The genetic platforms of Deinococcus species remain the only systems in which massive ionizing radiation (IR)-induced genome damage can be investigated in vivo at exposures commensurate with cellular survival. We report the whole genome sequence of the extremely IR-resistant rod-shaped bacterium Deinococcus ficus KS 0460 and its phenotypic characterization. Deinococcus ficus KS 0460 has been studied since 1987, first under the name Deinobacter grandis , then Deinococcus grandis . The D. ficus KS 0460 genome consists of a 4.019 Mbp sequence (69.7% GC content and 3894 predicted genes) divided into six genome partitions, five of which are confirmed to be circular. Circularity was determined manually by mate pair linkage. Approximately 76% of the predicted proteins contained identifiable Pfam domains and 72% were assigned to COGs. Of all D. ficus KS 0460 proteins, 79% and 70% had homologues in Deinococcus radiodurans ATCC BAA-816 and Deinococcus geothermalis DSM 11300, respectively. The most striking differences between D. ficus KS 0460 and D. radiodurans BAA-816 identified by the comparison of the KEGG pathways were as follows: (i) D. ficus lacks nine enzymes of purine degradation present in D. radiodurans , and (ii) D. ficus contains eight enzymes involved in nitrogen metabolism, including nitrate and nitrite reductases, that D. radiodurans lacks. Moreover, genes previously considered to be important to IR resistance are missing in D. ficus KS 0460, namely, for the Mn-transporter nramp , and proteins DdrF, DdrJ and DdrK, all of which are also missing in Deinococcus deserti . Otherwise, D. ficus KS 0460 exemplifies the Deinococcus lineage.
Genetics & Heredity↗