Deuterium enrichment using vanadium membranes

Hydrogen isotope selectivity of palladium membranes has long been known and studied, but the emergence of vanadium-based membranes as a low-cost alternative naturally inspires curiosity as to whether these membranes exhibit similar properties. Accordingly, experiments to calculate the permeability of hydrogen and deuterium through a palladium-coated vanadium membrane at 300 °C were undertaken, and they revealed that hydrogen permeates at a rate 1.5 × faster than deuterium. With hydrogen absorption experiments at the same temperature showing very little difference in the amount of each isotope absorbed over a wide pressure range, it can be concluded that atomic hydrogen diffuses through vanadium 1.5 × faster than atomic deuterium.In practice, this gives rise to a significant separation factor, with deuterium being depleted in the permeate stream, but enriched in the retentate stream. Creating a cascading series of membranes, with successive retentate streams combined, will allow the deuterium concentration to be enriched far beyond the natural value of 0.015%. This work suggests that further work is warranted to explore whether this separation factor can be enhanced (e.g., through alloying), and to demonstrate a cascading membrane system to deliver high purity deuterium from a natural hydrogen source.     

Anomalous steam oxidation behavior of a creep resistant martensitic 9 wt. % Cr steel

The efficiency of thermal power plants is currently limited by the long-term creep strength and the steam oxidation resistance of the commercially available ferritic/martensitic steel grades. Higher operating pressures and temperatures are essential to increase efficiency but impose important requirements on the materials, from both the mechanical and chemical stability perspective. It has been shown that in general, a Cr wt. % higher than 9 is required for acceptable oxidation rates at 650 °C, but on the other hand such high Cr content is detrimental to the creep strength. Surprisingly, preliminary studies of an experimental 9 wt. % Cr martensitic steel, exhibited very low oxidation rates under flowing steam at 650 °C for exposure times exceeding 20,000 h. A metallographic investigation at different time intervals has been carried out. Moreover, scanning transmission electron microscopy (STEM) analysis of a ground sample exposed to steam for 10,000 h at 650 °C revealed the formation of a complex tri-layered protective oxide comprising a top and bottom Fe and Cr rich spinel layer with a magnetite intermediate layer on top of a very fine grained zone.     

Stack performance of phosphotungstic acid functionalized mesoporous silica (HPW-meso-silica) nanocomposite high temperature proton exchange membrane fuel cells

In this paper, a series of short stacks with 2-cell, 6-cell and 10-cell employing phosphotungstic acid functionalized mesoporous silica (HPW-meso-silica) nanocomposite proton exchange membranes (PEMs) have been successfully fabricated, assembled and tested from room temperature to 200 °C. The effective surface area of the membrane was 20 cm² and fabricated by a modified hot-pressing method. With the 2-cell stack, the open circuit voltage was 1.94 V and it was 5.01 V for the 6-cell stack, indicating a low gas permeability of the HPW-meso-silica membranes. With the 10-cell stack, a maximum power density of 74.4 W (equivalent to 372.1 mW cm⁻²) occurs at 150 °C in H₂/O₂, and the stack produces a near-constant power output of 31.6 W in H₂/air at 150 °C without external humidification for 50 h. The short stack also displays good performance and stability during startup and shutdown cycling testing for 8 days at 150 °C in H₂/air. Although the stack test period may be too short to extract definitive conclusions, the results are very promising, demonstrating the feasibility of the new inorganic HPW-meso-silica nanocomposites as PEMs for fuel cell stacks operating at elevated temperatures in the absence of external humidification.     

A novel sequence-based antigenic distance measure for H1N1, with application to vaccine effectiveness and the selection of vaccine strains

H1N1 influenza causes substantial seasonal illness and was the subtype of the 2009 influenza pandemic. Precise measures of antigenic distance between the vaccine and circulating virus strains help researchers design influenza vaccines with high vaccine effectiveness. We here introduce a sequence-based method to predict vaccine effectiveness in humans. Historical epidemiological data show that this sequence-based method is as predictive of vaccine effectiveness as hemagglutination inhibition assay data from ferret animal model studies. Interestingly, the expected vaccine effectiveness is greater against H1N1 than H3N2, suggesting a stronger immune response against H1N1 than H3N2. The evolution rate of hemagglutinin in H1N1 is also shown to be greater than that in H3N2, presumably due to greater immune selection pressure.     

8-Aminoquinolines with an Aminoxyalkyl Side Chain Exert in vitro Dual-Stage Antiplasmodial Activity

A series of novel 8-aminoquinolines (8-AQs) with an aminoxyalkyl side chain were synthesized and evaluated for in vitro antiplasmodial properties against asexual blood stages, liver stages, and sexual stages of Plasmodium falciparum. 8-AQs bearing 2-alkoxy and 5-phenoxy substituents on the quinoline ring system were found to be the most promising compounds under study, exhibiting potent blood schizontocidal and moderate tissue schizontocidal in vitro activity.     

Hydrogen adsorption properties of carbide-derived carbons at ambient temperature and high pressure

Properties of the adsorbed hydrogen phase have been studied for hydrogen adsorption in three carbide derived carbons: SiC-CDC, steam/CO₂ activated SiC-CDC and TiC-CDC. Using the excess hydrogen uptake isotherm at hydrogen pressures above 120 MPa where adsorption has finished, the adsorbate volume has been determined and the adsorbate density has been calculated at ambient temperatures. Absolute adsorption isotherms have been constructed by assuming the adsorbate volume is equivalent to the pore volume and is therefore constant. This study indicates that all three CDCs had the same maximum adsorbate density, with the adsorption proportional to the total pore volume.     

Engineering Immunological Tolerance Using Quantum Dots to Tune the Density of Self‐Antigen Display

Treatments for autoimmunity—diseases where the immune system mistakenly attacks self‐molecules—are not curative and leave patients immunocompromised. New studies aimed at more specific treatments reveal that development of inflammation or tolerance is influenced by the form in which self‐antigens are presented. Using a mouse model of multiple sclerosis (MS), it is shown for the first time that quantum dots (QDs) can be used to generate immunological tolerance by controlling the density of self‐antigen on QDs. These assemblies display dense arrangements of myelin self‐peptide associated with disease in MS, are uniform in size (<20 nm), and allow direct visualization in immune tissues. Peptide‐QDs rapidly concentrate in draining lymph nodes, colocalizing with macrophages expressing scavenger receptors involved in tolerance. Treatment with peptide‐QDs reduces disease incidence tenfold. Strikingly, the degree of tolerance—and the underlying expansion of regulatory T cells—correlates with the density of myelin molecules presented on QDs. A key discovery is that higher numbers of tolerogenic particles displaying lower levels of self‐peptide are more effective for inducing tolerance than fewer particles each displaying higher densities of peptide. QDs conjugated with self‐antigens can serve as a new platform to induce tolerance, while visualizing QD therapeutics in tolerogenic tissue domains.     

Self‐Assembly of Immune Signals Improves Codelivery to Antigen Presenting Cells and Accelerates Signal Internalization,Processing Kinetics,and Immune Activation

Vaccines and immunotherapies that elicit specific types of immune responses offer transformative potential to tackle disease. The mechanisms governing the processing of immune signals—events that determine the type of response generated—are incredibly complex. Understanding these processes would inform more rational vaccine design by linking carrier properties, processing mechanisms, and relevant timescales to specific impacts on immune response. This goal is pursued using nanostructured materials—termed immune polyelectrolyte multilayers—built entirely from antigens and stimulatory toll‐like receptors agonists (TLRas). This simplicity allows isolation and quantification of the rates and mechanisms of intracellular signal processing, and the link to activation of distinct immune pathways. Each vaccine component is internalized in a colocalized manner through energy‐dependent caveolae‐mediated endocytosis. This process results in trafficking through endosome/lysosome pathways and stimulation of TLRs expressed on endosomes/lysosomes. The maximum rates for these events occur within 4 h, but are detectable in minutes, ultimately driving downstream proimmune functions. Interestingly, these uptake, processing, and activation kinetics are significantly faster for TLRas in particulate form compared with free TLRa. Our findings provide insight into specific mechanisms by which particulate vaccines enhance initiation of immune response, and highlight quantitative strategies to assess other carrier technologies.