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At least 451 records · Page 25

Compression of Acoustic Beams at Conversion Reflection in Hexagonal Crystals

It is shown how the entire energy of an acoustic beam incident on a boundary of a hexagonal crystal can be directed into a narrow reflected beam propagating at a small angle to the surface. This process is accompanied by mode conversion: the incident and reflected beams belong to different acoustic branches. The conversion near the total internal reflection is implemented by matching the orientations of the sagittal plane and surface and thereby eliminating the loss for parasitic wave reflection. The found conversion conditions and resonant reflection parameters are expressed in terms of the moduli of elasticity of crystal.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Foreshock wave interaction with the magnetopause: Signatures of mode conversion

Our previous hybrid simulation under a radial interplanetary magnetic field (IMF) and a supercritical solar wind Mach number has shown that foreshock compressional waves originated from the quasi–parallel (Q–∥) shock are mode converted to kinetic Alfvén waves (KAWs) at the Alfvén resonance surface of the subsolar magnetopause. In this paper, three–dimensional global dayside mode conversion is investigated for cases under various solar wind conditions using the global hybrid model. The global patterns and propagations of KAWs are distinguished and presented. Under a near–critical Mach number ( M A =3), KAW structures due to mode conversion exhibit a feature of broader excitation regions in the magnetopause boundary layer (MPBL) compared to supercritical Mach number ( M A =5) shocks. For cases with an oblique IMF with supercritical Mach numbers ( M A =5), the amplitude of magnetosheath compressional waves is larger at the quasi–parallel shock (Q–∥) than at the quasi–perpendicular (Q–⊥) shock. Downstream of the Q–∥ shock, there is a general trend that the perturbations of density ( N ) and magnetic field ( B ) change from predominantly in–phase in the magnetosheath to antiphase near the MPBL. While downstream of the Q–⊥ shock, an antiphase relation between N and B is dominant throughout the magnetosheath and magnetopause except near the shock transition. The compressional drivers are found to reach an extended region of the magnetopause due to the combined effects of wave propagation in the plasma frame and flow convection, leading to a broad region of mode conversion at the magnetopause. Subsequently, the resulting KAWs can be carried to the regions downstream of the Q–⊥ shock owing to the flow convection at the magnetopause. Furthermore the KAWs propagate poleward along the geomagnetic field lines and meanwhile are carried tailward by the ambient flows, and they are more intense in the downstream of Q–∥ shocks than downstream of Q–⊥ shocks.

79 ASTRONOMY AND ASTROPHYSICS↗

On the Balance of Intercalation and Conversion Reactions in Battery Cathodes

A thermodynamic analysis of the driving forces is presented for intercalation and conversion reactions in battery cathodes across a range of possible working ion, transition metal, and anion chemistries. Using this body of results, the importance of polymorph selection as well as chemical composition on the ability of a host cathode to support intercalation reactions is analyzed. It is found that the accessibility of high energy charged polymorphs in oxides generally leads to larger intercalation voltages favoring intercalation reactions, whereas sulfides and selenides tend to favor conversion reactions. Furthermore, it is observed that Cr-containing cathodes favor intercalation more strongly than those with other transition metals. It is concluded that two-electron reduction of transition metals (as is possible with the intercalation of a 2 + ion) will favor conversion reactions in the compositions studied.

25 ENERGY STORAGE↗

Total Protein Content Determination of Microalgal Biomass by Elemental Nitrogen Analysis and a Dedicated Nitrogen-to-Protein Conversion Factor

Accurately determining protein content is important in the valorization of algal biomass in food, feed, and fuel markets, where these values are used for component balance calculations. Conversion of elemental nitrogen to protein is a well-accepted and widely practiced method, but depends on developing an applicable nitrogen-to-protein conversion factor. The methodology reported here covers the quantitative assessment of the total nitrogen content of algal biomass and a description of the methodology that underpins the accurate de novo calculation of a dedicated nitrogen-to-protein conversion factor.

09 BIOMASS FUELS↗

Optimal design of a model energy conversion device

Fuel cells, batteries, and thermochemical and other energy conversion devices involve the transport of a number of (electro-) chemical species through distinct materials so that they can meet and react at specified multi-material interfaces. Therefore, morphology or arrangement of these different materials can be critical in the performance of an energy conversion device. In this paper, we study a model problem motivated by a solar-driven thermochemical conversion device that splits water into hydrogen and oxygen. We formulate the problem as a system of coupled multi-material reaction-diffusion equations where each species diffuses selectively through a given material and where the reaction occurs at multi-material interfaces. In conclusion, we introduce a phase-field formulation of the optimal design problem and numerically study selected examples.

30 DIRECT ENERGY CONVERSION↗

Optomechanical control of mode conversion in a hybrid semiconductor microcavity containing a quantum dot

The future of quantum communication systems and quantum networks heavily rely on the ability to fabricate and coherently control the conversion of photons between different modes based on a solid-state plateform. In this work, we propose and theoretically investigate a scheme to optomechanically control coherent mode conversion of optical photons by utilizing two optically coupled hybrid semiconductor microcavities containing a quantum dot (QD). One of the microcavity is pumped by an external laser and the second cavity is driven by light emitted by the QD that is embedded in the interface separating the two microcavities. The semiconductor microcavities can be fabricated using distributed Bragg reflectors and can be made movable. We have demonstrated that photon-mode-conversion efficiency can be coherently manipulated by the optomechanical mode under appropriate conditions.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

Spectral emittance measurements of micro/nanostructures in energy conversion: a review

Micro/nanostructures play a key role in tuning the radiative properties of materials and have been applied to the high-temperature energy conversion systems for improved performance. Among the various radiative properties, spectral emittance is of integral importance for the design and analysis of materials that function as radiative absorbers or emitters. This article presents an overview of the spectral emittance measurement techniques using both the direct and indirect methods. Several micro/nanostructures are also introduced, and a special emphasis is placed on the emissometers developed for characterizing engineered micro/nanostructures in high-temperature applications (e.g., solar energy conversion and thermophotovoltaic devices). Both experimental facilities and measured results for different materials are summarized. Future prospects in developing instrumentation and micro/nanostructured surfaces for practical applications are also outlined. This study provides a comprehensive source of information for the application of micro/nanostructures in high-temperature energy conversion engineering.

14 SOLAR ENERGY↗

Chapter 21: Sustainable Technologies for Seaweed Conversion to Biofuels and Bioproducts

Seaweeds are attractive candidates to supply the future sustainable, photosynthetic, bioenergy feedstocks thanks to their cultivation promise in offshore marine farms, with year-round production, and no external nutrient requirements. Despite this potential, there are significant challenges associated with realizing both the cultivation and harvesting logistics, as well as in developing an efficient conversion platform to fuels and products. Effective and scalable and economically viable conversion processes tailored to a seaweed are discussed in detail and gaps on identified needs for yield and efficiency improvements. Among the conversion processes discussed here, anaerobic fermentation of seaweeds to bioenergy products, including organic acids and biomass, is promising to disrupt the current bioenergy landscape.

anaerobic digestion↗

A Low-Enriched Uranium (LEU) option for the conversion of FRM II

The Forschungs-Neutronenquelle Heinz Maier-Leibnitz (FRM II) is Germany’s most powerful research reactor and uses Highly Enriched Uranium (HEU) fuel enriched at 93 %. The Technical University of Munich (TUM) operates the reactor and has been mandated to convert the FRM II to a lower-enrichment fuel. In preparation for the lower-enrichment fuel downselection, planned for 2023, TUM is evaluating multiple conversion scenarios. In this paper, it is demonstrated that a conversion of FRM II to Low-Enriched Uranium (LEU) is scientifically possible when using the novel monolithic U-10Mo fuel system, which is currently in the qualification process. As a research reactor, safety criteria, neutron flux distribution and cycle length are key metrics. To begin, neutronic and thermal-hydraulic models were created based on current technical drawings and relevant material properties. Specifically tailored computational methods and coupling schemes have also been developed to properly evaluate all relevant characteristics for the conversion of the FRM II reactor. Using these models and methods, a systematic parameter study was performed to explore the defined design space. The results of that study indicate that many LEU designs using monolithic U-10Mo appear to be viable to convert FRM II to LEU. One example of an LEU solution for the FRM II reactor that fulfills the stated safety, compatibility and scientific performance requirements is discussed in more detail.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗

Electrochemical conversion of methane to ethylene, olefins, and paraffins using metal-supported solid oxide cells

Electrochemical oxidative coupling of methane (E-OCM) with Sr 2 Fe 1·5 Mo 0·5 O 6–δ (SFM) catalyst is demonstrated with metal-supported solid oxide cells (MS-SOC). SFM anode and Pr 6 O 11 cathode catalysts are loaded into a porous symmetric-architecture cell by infiltration and firing. The most effective chelating agent (citric acid/ethyl glycol) and optimal firing/reducing temperatures (850 °C/750 °C) for the SFM catalyst precursor solution are selected and confirmed by cell testing. Operating temperature, cell voltage, and oxygen concentration at the cathode greatly affect the methane conversion rate and product selectivity by controlling the oxygen ion flow. CH 4 conversion of 85.8% is obtained, with C 2 H 4 , C 2 H 6 , and H 2 concentrations of 10.5%, 12.3%, and 25.6% at 800 °C, respectively, in the product exhaust gas. Reasonable stability of the current density and methane conversion is demonstrated during 200 h operation. Furthermore, this research demonstrates technical progress in catalyst and device development for the E-OCM reaction to synthesize valuable chemicals.

30 DIRECT ENERGY CONVERSION↗

Facile and low cost oxidative conversion of MoS{sub 2} in α-MoO{sub 3}: Synthesis, characterization and application

This study describes a facile low cost route to synthesize the α-MoO{sub 3} through a conversion of the precursor MoS{sub 2} in oxidant media. The structure and morphology of the α-MoO{sub 3} were studied by high resolution transmission electron microscopy (HRTEM) and selected area electron diffraction (SAED), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. The results show that α-MoO{sub 3} was obtained with reduced size, high purity, strongly-preferred orientation and structural defects, which ensures versatility and multifunctionality to this sample. For the purpose of applications, α-MoO{sub 3} was successfully employed in inverted organic solar cells devices as a possible alternative to the PEDOT:PSS in the hole transportation layer. - Graphical abstract: Synthesis process based on low cost oxidative conversion of MoS{sub 2} in α-MoO{sub 3} Display Omitted - Highlights: • A facile route to obtain α-MoO{sub 3} by refluxing the MoS{sub 2} precursor in oxidant media. • High purity and strongly-preferred orientation. • Belt-shaped material. • Enhanced conversion efficiency (PCE) when compared with conventional PEDOT:PSS.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Enhancing the photothermal conversion efficiency of graphene oxide by doping with NaYF4: Yb, Er upconverting luminescent nanocomposites

Highlights: • An experimental setup of measuring the temperature profile was established. • A new calculating modeling of photothermal conversion efficiency was set up. • The photothermal conversion efficiency of GO could be enhanced by doping NaYF{sub 4}: Yb, Er and the mechanism is discussed. - Abstract: Graphene oxide/NaYF{sub 4}: Yb, Er nanocomposites have been synthesized via hydrothermal synthesis, in which spherical cubic phase NaYF{sub 4}: Yb, Er nanocrystals with uniformity are implanted onto the surface of graphene oxide (GO). Using a near infrared laser set to 980 nm, the light-to-heat energy transfer efficiency of GO/NaYF{sub 4}: Yb, Er is 13.9% higher than GO by itself, revealing that the photothermal conversion efficiency of GO could be enhanced by doping NaYF{sub 4}: Yb, Er nanocrystals. This phenomenon can be attributed to the energy transfer between the NaYF{sub 4}: Yb, Er nanocrystals to the energy receptor in the GO substrate.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Validation of gamma-ray detection techniques for safeguards monitoring at natural uranium conversion facilities

Recent IAEA circulars and policy papers have sought to implement safeguards when any purified aqueous uranium solution or uranium oxides suitable for isotopic enrichment or fuel fabrication exists. Under the revised policy, IAEA Policy Paper 18, the starting point for nuclear material under safeguards was reinterpreted, suggesting that purified uranium compounds should be subject to safeguards procedures no later than the first point in the conversion process. In response to this technical need, a combination of simulation models and experimental measurements were employed to develop and validate concepts of nondestructive assay monitoring systems in a natural uranium conversion plant (NUCP). In particular, uranyl nitrate (UO 2 (NO 3 ) 2 ) solution exiting solvent extraction was identified as a key measurement point (KMP), where gamma-ray spectroscopy was selected as the process monitoring tool. The Uranyl Nitrate Calibration Loop Equipment (UNCLE) facility at Oak Ridge National Laboratory was employed to simulate the full-scale operating conditions of a purified uranium-bearing aqueous stream exiting the solvent extraction process in an NUCP. Nondestructive assay techniques using gamma-ray spectroscopy were evaluated to determine their viability as a technical means for drawing safeguards conclusions at NUCPs, and if the IAEA detection requirements of 1 significant quantity (SQ) can be met in a timely way. This work investigated gamma-ray signatures of uranyl nitrate circulating in the UNCLE facility and evaluated various gamma-ray detector sensitivities to uranyl nitrate. These detector validation activities include assessing detector responses to the uranyl nitrate gamma-ray signatures for spectrometers based on sodium iodide, lanthanum bromide, and high-purity germanium detectors. The results of measurements under static and dynamic operating conditions at concentrations ranging from 10–90 g U/L of natural uranyl nitrate are presented. A range of gamma-ray lines is examined, including attenuation for transmission measurement of density and concentration. It was determined that transmission-corrected gamma-ray spectra provide a reliable way to monitor the 235 U concentration of uranyl nitrate solution in transfer pipes in NUCPs. Furthermore, existing predictive and analysis methods are adequate to design and realize practical designs. The 137 Cs transmission source employed in this work is viable but not optimal for 235 U densitometry determination. Validated simulations assessed the viability of 133 Ba and 57Co as alternative densitometry sources. All three gamma-ray detectors are viable for monitoring natural uranium feed; although high-purity germanium is easiest to interpret, it is, however, the least attractive as an installation instrument. Overall, for monitoring throughput in a facility such as UNCLE, emulating the uranium concentration and pump speeds of the Springfields conversion facility in the United Kingdom, an uncertainty of less than 0.17% is required in order to detect the diversion of 1 SQ of uranyl nitrate through changes in uranium concentration over an accountancy period of one year with a detection probability of 50%. As a result, calibrated gamma-ray detection systems are capable of determining the concentration of uranium content in NUCPs, it is only in combination with verifiable operator declarations and supporting data, such as flow rate and enrichment, that safeguards conclusions can be drawn.

98 NUCLEAR DISARMAMENT, SAFEGUARDS, AND PHYSICAL P↗

Biological conversion of methane to methanol at high H 2 S concentrations with an H 2 S-tolerant methanotrophic consortium

To develop biological biogas to methanol conversion technology without costly hydrogen sulfide (H 2 S) removal, a high H 2 S tolerant methanotrophic consortium (HTMC), was enriched from an anaerobic digester effluent in presence of 5.64 g/m 3 H 2 S in the gas phase. The HTMC can grow stably and produce methanol under conditions with CH 4 /air mixtures containing 5.64 g/m 3 of H 2 S. There is no significant (p>0.05) difference in cell yield or CH 4 to methanol conversion efficiency between trials with different H 2 S concentrations from 0 g/m 3 to 5.64 g/m 3 . Further, under optimal conditions, a cell yield of 0.333 g cells/g CH 4 , a methanol concentration of 0.28 mg/mL, and a CH 4 to methanol conversion efficiency of 0.22 mol/mol were obtained, respectively. Besides methanotrophs (14.85%) and other bacteria, Cyanobacteria were also identified in the HTMC with a high abundancy (32.16%), which could broaden the application of HTMC for simultaneous utilization of CH 4 and CO 2 from raw biogas.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Carbon Dioxide Conversion to Nanomaterials: Methods, Applications, and Challenges

Anthropogenic carbon dioxide (CO 2 ) emission is one of the biggest global threats that we are confronted with in the 21st century. A lack of prompt action to mitigate the atmospheric CO 2 level could lead to global catastrophic events. As a result of the significance of the aforementioned threat, multiple nations have agreed to enact carbon capture, storage, utilization, and sequestration (CCUS) technologies at academic and industrial scales with the aim of lowering the atmospheric CO 2 level. Although there are many reviews on CCUS technologies, there is a lack of comprehensive review on CO 2 conversion to more economically valuable products, such as nanomaterials. Carbon dioxide capture and conversion into nanomaterials is an interesting research topic in many ways because it contributes to our fundamental knowledge of material conversion, provides alternative ways to reduce atmospheric pollution, and yields lucrative products, which has not been explored broadly. Aside from the positive outcomes, we have a moral obligation to rectify a global threat caused by anthropogenic emission. Herein, we present current methods of converting CO 2 into organic and inorganic nanomaterials with a focus on operating conditions and challenges as well as the potential of nanomaterials in specifically biomedical applications as opposed to extensively reviewed energy-related uses. Furthermore, our review emphasizes the toxicity issues related to using such nanomaterials in biological settings based on literature and other comparable studies.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Improving Conversion of Captured CO 2 on Mixed-Oxide Dual-Function Materials by Low-Concentration Metal Promotion

Reactive carbon capture (RCC) is a promising nascent approach to harness the untapped resource of waste CO 2 to produce fuels and platform chemicals. However, process economics relies on the design of dual-function materials (DFMs) that exhibit maximal conversion of captured CO 2 and high selectivity toward valuable carbon products (e.g., CO). Herein, we report the use of low-concentration (ca. 0.5 wt %) metal promotors (Pt and Au) to improve the conversion of captured CO 2 on a Zn-Al mixed-oxide DFM by >30%, while also more than doubling per-cycle CO yield due to enhanced retention of captured CO 2 and H 2 activation. In situ DRIFTS of bound CO 2 on the DFMs showed distinctions in surface carbonate formation for the Pt- and Au-modified materials that were correlated with product evolution during the reactive desorption step of RCC. Particularly, Pt afforded superior H 2 activation but formed irreversibly-bound bicarbonates, compromising overall productivity, while the Na/Au/ZA DFM predominantly adsorbed CO 2 on Na sites, resulting in polydentate carbonates that are retained until higher temperatures before conversion to CO. In conclusion, these results indicate that adding a low concentration of oxidation-resistant noble metals, especially Au, is an effective strategy for improving key performance metrics of Zn-Al mixed-oxide DFMs to further advance the development of scalable RCC technologies.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Room-Temperature Pseudo-Solid-State Iron Fluoride Conversion Battery with High Ionic Conductivity

Li-metal batteries (LMBs) employing conversion cathode materials (e.g., FeF 3 ) are a promising way to prepare inexpensive, environmentally friendly batteries with high energy density. Pseudo-solid-state ionogel separators harness the energy density and safety advantages of solid-state LMBs, while alleviating key drawbacks (e.g., poor ionic conductivity and high interfacial resistance). In this work, a pseudo-solid-state conversion battery (Li-FeF 3 ) is presented that achieves stable, high rate (1.0 mA cm –2 ) cycling at room temperature. The batteries described herein contain gel-infiltrated FeF 3 cathodes prepared by exchanging the ionic liquid in a polymer ionogel with a localized high-concentration electrolyte (LHCE). The LHCE gel merges the benefits of a flexible separator (e.g., adaptation to conversion-related volume changes) with the excellent chemical stability and high ionic conductivity (~2 mS cm –1 at 25 °C) of an LHCE. The latter property is in contrast to previous solid-state iron fluoride batteries, where poor ionic conductivities necessitated elevated temperatures to realize practical power levels. Importantly, the stable, room-temperature Li-FeF 3 cycling performance obtained with the LHCE gel at high current densities paves the way for exploring a range of architectures including flexible, three-dimensional, and custom shape batteries.

25 ENERGY STORAGE↗

Environmentally Friendly Zr-Based Conversion Nanocoatings for Corrosion Inhibition of Metal Surfaces Evaluated by Multimodal X-ray Analysis

Chemical conversion coating as an effective corrosion inhibition has wide range of applications in industries and is of great expectation to be environmentally friendly and cost-effective. Zirconium-based (Zr-based) conversion coating using hexafluorozirconic acid with copper (Cu) additive on low carbon steel which improves anticorrosion and adhesion properties was studied using synchrotron X-ray and electron-based techniques. To understand the elemental evolution during coating formation process, in situ synchrotron X-ray fluorescence (XRF) microscopy has been applied to observe Zr, Cu, iron (Fe), and zinc (Zn) concentration evolution. By quantifying the density, average size, and size distribution of the cluster as a function of time and temperature, the growth mechanism of the coating can be concluded as a reaction-controlled mechanism. X-ray absorption near edge structure and X-ray photoelectron spectroscopy (XPS) were used to characterize the composition of the Cu-rich clusters embedded in the coating which was determined to be mainly Cu 2 O, Cu, and CuF 2 ; the cluster composition varies from the surface to the internal region as determined by the depth-profiling of XPS. Our study shed light on the chemical and morphological evolution in environmentally friendly surface conversation coating and demonstrated new methodology in studying the coating formation via in situ synchrotron XRF.

36 MATERIALS SCIENCE↗