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At least 235 records · Page 13

Aerogel with Unparalleled Performance and Cost-Effectiveness for All Insulation Needs (CRADA Final Report)

Westwood Aerogel investigated the reproducible production of an ambiently or electromagnetic spectrum assisted drying of extremely porous aerogel materials. Traditional aerogel processing is limited by low throughput and scalability due to supercritical drying. Westwood Aerogel’s advanced manufacturing process enables commercialization and deployment at scale, making aerogel materials more accessible to a range of industries and applications. We focused on shifting from the lab scale environment to manufacturing prototypes. The initial manufacturing model is based on the float glass process, which is the industry standard for glass window production, and the paper drying process. By incorporating an ambient drying process a continuous line model can be used from start to finish. The project team worked to develop a continuous manufacturing system to scale-up and reduce costs while maintaining the lightweight and insulative properties of aerospace-grade aerogel. While aerogels are extremely insulative, lightweight, and thin materials (making them ideal insulators across application spaces), high costs and stagnant innovation have hampered their wider adoption. Traditional manufacturing of aerogel requires supercritical extraction of pore fluid to obtain highly insulating materials, which is an energy intensive batch process and limits aerogel production output. Westwood Aerogel’s proprietary ambient drying process enables the continuous production of highly insulative aerogel materials without the use of supercritical extraction.

36 MATERIALS SCIENCE↗

Assessment of desalination technologies for treatment of a highly saline brine from a potential CO 2 storage site

Brine extraction is a promising strategy for the management of increased reservoir pressure, resulting from carbon dioxide (CO 2 ) injection in deep saline reservoirs. The extracted brines usually have high concentrations of total dissolved solids (TDS) and various contaminants, and require proper disposal or treatment. In this article, first by conducting a critical review, we evaluate the applicability, limits, and advantages or challenges of various commercially available and emerging desalination technologies that can potentially be employed to treat the highly saline brine (with TDS values >70.000 ppm) and those that are applicable to a ~200,000 ppm TDS brine extracted from the Mt. Simon Sandstone, a potential CO 2 storage site in Illinois, USA. Based on the side-by-side comparison of technologies, evaporators are selected as the most suitable existing technology for treating Mt. Simon brine. Process simulations are then conducted for a conceptual design for desalination of 454 m 3 /h (2000 gpm) pretreated brine for near-zero liquid discharge by multi-effect evaporators. In conclusion, the thermal energy demand is estimated at 246kWh perm 3 of recoveredwater, ofwhich 212kWh/m 3 is required for multiple-effect evaporation and the remainder for salt drying. The process also requires additional electrical power of ~2 kWh/m 3 .

42 ENGINEERING↗

Application of a Dual-Column Method to Selectively Extract and Purify Berkelium-249 from Other Actinides and Impurities

The super heavy element (SHE) Tennessine (Ts, Element 117) was discovered in 2016 a collaboration of US and Russian scientists vis bombardment reaction of 249 Bk + 48 Ca $\rightarrow$ 117 Ts, while the target element 249 Bk (half-life 330d) was produced and provided by the Radiochemical Engineering Development Center (REDC), Oak Ridge National Laboratory (ORNL). The production of 249 Bk at REDC, ORNL requires a multi-step chemical process of irradiated curium feedstock target to remove all fission product (FP) elements and to separate 249 Bk from other actinide (An) elements (Am, Cm, Cf, Fm and Es), including: Caustic Dissolution, Acid Dissolution, Cleanex, two LiCl Anion Exchanges, LiOH Precipitation, Cation Exchange with AHIB, and with Bk Finishing as the final Bk purification step. The major product of this campaign is 252 Cf, while 249 Bk is one of important by-products. The current Cf campaign for recovery of c.a. 15 mg of 249 Bk per campaign (not including the time for Finishing of Cf, Fm and Es) takes 6 or 7 months, including ~3 months spent on Bk Finishing. Bk Finishing includes two major processes: (1) BERKEX, operated inside a hot cell with two cycles of batch solvent extraction (SX) using di-2-ethylhexyl phosphoric acid (HDEHP) as the extractant for tetravalent 249 Bk from an 8 $M$ HNO 3 -0.3 $M$ NaBrO 3 solution; and (2) Cation Exchange (CX) with AHIB (α-Hydroxy isobutyric acid), operated inside a glove box laboratory. Entire Bk Finishing takes five SX, more than five column runs and several drying down processes for aqueous solutions including one from 500 mL to 1 mL for volume reduction. To shorten the Bk Finishing period and simplify the Bk purification operation steps, possibilities of using other resin columns were explored.Recent trials using columns of either $LN$ resin or $MP$-1 anion exchange resin adsorbing the tetravalent 249 Bk 4+ in 8 $M$ HNO 3 -0.5 $M$ NaBrO 3 , followed by eluting impurities (e.g. Ce 4+ ,Cf 3+ ) and stripping 249 Bk resulted in a new Dual Column Method of selectively separating 249 Bk from other trans-plutonium elements and fission product (FP) impurities. This new method is proposed to replace the current Bk Finishing and provide increased Bk purification effeciency and a shorter processing period of 4 to 5 months (less decay loss for higher 249 Bk productivity). This TM Report discusses the trial experimental results, describes the dual column method with relevant chemistry issues and possibilities being used in further process steps ahead of the Bk Finishing.

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗

Conversion of a wet waste feedstock to biocrude by hydrothermal processing in a continuous-flow reactor: grape pomace

Wet waste feedstocks present an apt opportunity for biomass conversion to fuels by hydrothermal processing. In this study, grape pomace slurries from two varieties, Montepulciano and cabernet sauvignon, have been converted into a biocrude by hydrothermal liquefaction (HTL) in a bench-scale, continuous-flow reactor system. Carbon conversion to gravity-separable biocrude product up to 56 % was accomplished at relatively low temperature (350 C) in a pressurized (sub-critical liquid water) environment (20 MPa) when using grape pomace feedstock slurry with a 16.8 wt% concentration of dry solids processed at a liquid hourly space velocity of 2.1 h-1. Direct oil recovery was achieved without the use of a solvent and biomass trace mineral components were removed by processing steps so that they did not cause processing difficulties. In addition, catalytic hydrothermal gasification (CHG) was effectively applied for HTL byproduct water cleanup using a Ru on C catalyst in a fixed bed producing a gas composed of methane and carbon dioxide from water soluble organics. Conversion of 99.8% of the chemical oxygen demand (COD) left in the aqueous phase was demonstrated. As a result, high conversion of grape pomace to liquid and gas fuel products was found with residual organic contamination in byproduct water reduced to <150 mg/kg COD.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

Fabric properties and electric efficiency limits of mechanical moisture extraction from fabrics

Residential clothes drying consume about 650 TBtu of primary energy per year in the United States, equivalent to 3% of primary residential energy consumption. There is a strong impetus to reduce the energy consumption of clothes dryers by both improving existing technology and developing alternatives that use fundamentally different drying mechanisms. Clothes drying technologies are broadly classified into either evaporative or mechanical drying. The focus of this paper is on mechanical drying, including vibrational, centrifugal, and press-based methods. In this work, the physical processes involved in these mechanical fabric drying processes were analyzed to develop general theories of mechanical cloth drying energy efficiency. Quantitative evaluation of the theories requires measured fabric properties. To accomplish this, a set of experiments was conducted on samples of a standard test fabric. The fabric was a cotton-polyester blend specified by the US Department of Energy to evaluate the standardized efficiency of all residential clothes dryers in the US. Mercury porosimetry experiments were conducted to determine the fabric pore size distribution, apparent density, and porosity. Elasticity experiments were conducted to determine the fabric’s Young’s modulus. Isostatic press experiments were conducted to establish a relationship between compression force and fabric moisture content. The data resulting from these experiments were combined with mathematical models developed in this work to calculate the theoretical maximum performance limits for mechanical drying of the standard fabric. The results of the analysis are used to make recommendations for the most promising technologies that offer the greatest potential energy savings for residential clothes drying.

36 MATERIALS SCIENCE↗

Black hole and galaxy coevolution from continuity equation and abundance matching

We investigate the coevolution of galaxies and hosted supermassive black holes (BHs) throughout the history of the universe by a statistical approach based on the continuity equation and the abundance matching technique. Specifically, we present analytical solutions of the continuity equation without source terms to reconstruct the supermassive BH mass function from the active galactic nucleus (AGN) luminosity functions. Such an approach includes physically motivated AGN light curves tested on independent data sets, which describe the evolution of the Eddington ratio and radiative efficiency from slim- to thin-disk conditions. We nicely reproduce the local estimates of the BH mass function, the AGN duty cycle as a function of mass and redshift, along with the Eddington ratio function and the fraction of galaxies with given stellar mass hosting an AGN with given Eddington ratio. We exploit the same approach to reconstruct the observed stellar mass function at different redshift from the ultraviolet and far-IR luminosity functions associated with star formation in galaxies. These results imply that the build-up of stars and BHs in galaxies occurs via in situ processes, with dry mergers playing a marginal role at least for stellar masses ≲3×10{sup 11} M{sub ⊙} and BH masses ≲10{sup 9} M{sub ⊙}, where the statistical data are more secure and less biased by systematic errors. In addition, we develop an improved abundance matching technique to link the stellar and BH content of galaxies to the gravitationally dominant dark matter (DM) component. The resulting relationships constitute a testbed for galaxy evolution models, highlighting the complementary role of stellar and AGN feedback in the star formation process. In addition, they may be operationally implemented in numerical simulations to populate DM halos or to gauge subgrid physics. Moreover, they may be exploited to investigate the galaxy/AGN clustering as a function of redshift, mass, and/or luminosity. In fact, the clustering properties of BHs and galaxies are found to be in full agreement with current observations, thus further validating our results from the continuity equation. Finally, our analysis highlights that (i) the fraction of AGNs observed in the slim-disk regime, where most of the BH mass is accreted, increases with redshift; and (ii) already at z≳6 a substantial amount of dust must have formed over timescales ≲10{sup 8} yr in strongly star-forming galaxies, making these sources well within the reach of ALMA surveys in (sub)millimeter bands.

79 ASTRONOMY AND ASTROPHYSICS↗

Application of Black Silicon for Nanostructure-Initiator Mass Spectrometry

Nanostructure-initiator mass spectrometry (NIMS) is a matrix-free desorption/ionization technique with high sensitivity for small molecules. Surface preparation has relied on hydrofluoric acid (HF) electrochemical etching which is undesirable given the significant safety controls required in this specialized process. Here in this study, we examine a conventional and widely used process for producing black silicon based on sulfur hexafluoride/oxygen (SF 6 /O 2 ) inductively coupled plasma (ICP) etching at cryogenic temperatures and we find it to be suitable for NIMS. A systematic study varying parameters in the plasma etching process was performed to understand the relationship of black silicon morphology and its sensitivity as a NIMS substrate. The results suggest that a combination of higher silicon temperature and oxygen flow rate gives rise to the formation of black silicon with fine pillar structures, whose aspect ratio are ~8.7 and depth are <1 μm resulting in higher NIMS sensitivity which is attributed to surface restructuring caused by their low melting point upon laser irradiation. Interestingly, we find selectivity of these black silicon substrates to different analytes depending on the etching parameters. Though, the sensitivity of the dry etching process is lower than the traditional "wet" electrochemical etching process, it is suitable for many applications and is prepared using conventional equipment without the use of HF.

36 MATERIALS SCIENCE↗

In-line measurements of below-the-surface food deformation during drying with an interference-based optical fiber strain sensor

Real-time measurements of food deformation are important for quality control in drying, yet they pose significant challenges. In this study, we developed an interference-based optical fiber strain sensor to enable in-line, continuous, below-the-surface strain measurements in drying of soft food samples. Compared to a strain resolution of 8 × 10 -4 at zero strain and 7.2 × 10 -3 at 0.20 strain reported in our previously published work, the present study achieves markedly improved resolutions of 1.3 × 10 -4 at zero strain and 7.8 × 10 -4 at 0.25 strain, which strains are the lower and higher boundaries of the dynamic range, respectively. This nearly order-of-magnitude improvement is attributed to the unique interference-based sensing mechanism, no need for calibration to convert optical signals to strain, and the system-design-enabled immunity to fiber-disk misalignments and light source intensity fluctuations. To demonstrate the in-line process monitoring, deformation measurements of fresh banana slices and sugar cookie doughs were carried out in a benchtop oven and an industrial-scale hot-air pilot dryer, respectively. In both dryers, strain measurements were continuously measured during the whole drying process at various depths and radii below the sample surfaces, with the strains up to 25%. Computer vision was used only in the benchtop drying to confirm the faithfulness of the fiber sensor measurements and cannot provide below-the-surface measurements. The measured spatiotemporal deformation allowed us to confirm the shell-hardening effect and to determine the speed and location of large deformation changes in the whole drying process, the latter of which is related to the sample cracking. To the best of the authors’ knowledge, this study is the first to report on an interferometry-based fiber sensor to measure food deformation. This sensor and the sensing mechanism have high potential for real-time process monitoring and control to prevent over-drying or cracking during drying processes.

47 OTHER INSTRUMENTATION↗

Roll Compaction of Powdered Radioactive Wastes - 18251

Most of low- and intermediate-level radioactive wastes must be solidified by a proper binding matrix and disposed at the centralized disposal site. So it is desirable to achieve a high loading of radwastes in a drum to reduce the disposal fee while meeting both the national regulations and the waste acceptance criteria of the disposal site. In general, the radioactive wastes (liquid, dried powder and sludge) were solidified by mixing with a proper binding matrix (cement, polymer, asphalt, etc.), but their solidified volume inevitably increases due to the limitation of incorporating of radwaste into a binding matrix. To solve this problem, some Korean NPPs operate both a CTS (Concentrate Treatment System, evaporation and granulation) and a polymer solidification system. The size distribution of granulated wastes produced by CTS is so broad (diameter; several μm ∼ several cm) that a polymer cannot impregnate the void space between particles due to their small size. However, if the powdered radwaste can be compacted into high density pellets, and the pellets can be loaded in a drum with maximum waste loading, then the binding matrix can fill the void between pellets, it might be more desirable to keep the size distribution of pellets constant to reduce the solidified waste volume. This compaction methodology can greatly reduce the disposal fee due to the reduction of the solidified waste volume, and can facilitate polymer solidification due to the constant size of the radwaste pellets. This methodology is also applicable to solidify powdered wastes such a depleted uranium used as a catalyst, ash and sludge. Loading radwaste compacted with bentonite pellets versus particles into a container serves, as an engineered or natural barrier in a deep geologic disposal system. Roll compaction is a typical agglomeration process for dry powders and depends on the device parameters and the material properties. This study, firstly, was focused on the design of roll compactor (briquetting machine), the shape and size of pellet, and secondly the loading method of pellets into a drum, their solidification in polymer, and evaluating the overall volume reduction. We used bentonite (particle size; 85 ∼ 100 μm) as a material to be compacted instead of radwaste powders (concentrates and depleted uranium wastes) without the addition of agglomeration agents. In the design of roll, we considered the diameter (200 mm) and width (41 mm) of roll, two types of pocket shapes (< 9 mm, 0.275 ml), and the surface of the pocket. Fig. 2 shows two pellet shapes, tetragonal and circular. The pressure of roll compactor, one of the main process variables, is > 320 kg f/cm{sup 2}, and the roll gap is 0.5 mm. The powders are compacted in a compaction zone between two counter-rotating rolls according to the complicated mechanisms. As a result of the state and the apparent density of the pellets obtained by changing the pressure from 0 to 286 kg f/cm{sup 2}, the pellets were unstable at pressure=0, but above 148 kg f/cm{sup 2} the pellets were more stable, and the apparent density of the pellets was 2.63 g/cm{sup 3} at 148 kg f/cm{sup 3}, and 2.68 g/cm{sup 3} at 286 kg f/cm{sup 2}. The roller speed (rpm) can determine the capacity (kg/h) of a compactor, and depends on both the compaction pressure and the feeding rate. By increasing the roll speed from 2 to 4 rpm, the apparent density of pellets was decreased gradually from 2.74 g/cm{sup 3} to 1.45 g/cm{sup 3}. We designed the special feeding system in order to feed powders uniformly to the roll gripping zone and to supply powders into the narrowest part of the roll gap. At a constant roll speed (3 rpm) and a constant compaction pressure (286 kg f/cm{sup 2}), the apparent density of the pellets was linearly proportional to the feeding rate from 2.18 to 2.74 g/cm{sup 3} by changing the feeding rate of powders from 8 to 12 rpm. In the polymer solidification of the obtained pellets, we used epoxy resin as a solidification agent, and showed their solidified waste forms in Fig. 5. The incorporation ratio (wt.%) of powders/polymer was about 71.7/28.3 in tetragonal pellets, 71.9/28.1 in circular pellets. We calculated the volume reduction in an aspect of powders itself and the solidified waste form. In powder case, through the comparison of the apparent density of the obtained pellets (2.74 g/cm{sup 3}) and raw powders (0.93 g/cm{sup 3}), the volume reduction was calculated as about 2.74/0.93 = 2.95 times. This means that powders can be compacted to 1/2.95 times. And in waste form case, the weight ratio of powder/polymer in a mixing method (workable) and a compaction method is about 0.42, 2.56, individually. Therefore the volume reduction was calculated as about 2.56/0.42 = 6.01 times. We found a compaction methodology for the volume reduction of powdered radioactive wastes, and their polymer solidification will be more effective to reduce the volume of radwastes to be disposed. After a characterization of the solidified waste form incorporated pellets (including sintered pellets), this methodology will be applied to treat depleted uranium wastes used as catalyst, and to solve the problem of NPPs' polymer solidification system, as mentioned above. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

A Novel Laser 3D Printing Method for the Advanced Manufacturing of Protonic Ceramics

Protonic ceramics (PCs) with high proton conductivity at intermediate temperatures (300–600 °C) have attracted many applications in energy conversion and storage devices such as PC fuel/electrolysis cells, PC membrane reactors, hydrogen pump, hydrogen or water-permeable membranes, and gas sensors. One of the essential steps for fulfilling the practical utilization of these intermediate-temperature PC energy devices is the successful development of advanced manufacturing methods for cost-effectively and rapidly fabricating them with high energy density and efficiency in a customized demand. In this work, we developed a new laser 3D printing (L3DP) technique by integrating digital microextrusion-based 3D printing and precise and rapid laser processing (sintering, drying, cutting, and polishing), which showed the capability of manufacturing PCs with desired complex geometries, crystal structures, and microstructures. The L3DP method allowed the fabrication of PC parts such as pellets, cylinders, cones, films, straight/lobed tubes with sealed endings, microchannel membranes, and half cells for assembling PC energy devices. The preliminary measurement of the L3DP electrolyte film showed a high proton conductivity of ≈7 × 10−3 S/cm. This L3DP technique not only demonstrated the potential to bring the PCs into practical use but also made it possible for the rapid direct digital manufacturing of ceramic-based devices.

08 HYDROGEN↗

Increasing the Hot‐Electron Driven Hydrogen Evolution Reaction Rate on a Metal‐Free Graphene Electrode

Abstract Recently, it has been shown that a semiconductor–insulator–graphene device can drive the hydrogen evolution reaction (HER) at the graphene surface with a reduced onset potential by injecting hot electrons into graphene. However, the catalytic properties of graphene are limited by the large hydrogen adsorption energy and lack of electrochemically active sites. To address these limitations, a n ‐silicon/insulator/plasma etched graphene device is investigated, where a dry etch process is used to increase the number of active sites on the graphene by creating a greater number of active edge sites, increasing hydrogen adsorption at a given potential. This has been shown to improve the properties of devices with cold electrons. However, here it is shown that this approach can improve the HER rate with hot electrons. The electrons injected into the graphene from the silicon shift the onset potential of HER by as high as ≈0.8 V reaching a current density of 90 mA cm −2 at an overpotential of ‐0.5 V versus RHE. Furthermore, the comparison between device with pristine graphene shows a ≈2X improvement in current density at high overpotentials. This result shows that hot‐electron devices can be improved by modifying the catalytically active sites without metal catalysts.

Chae, Hyun Uk↗

Carbon-Assisted, Continuous Syngas Production in a Chemical Looping Scheme

In the current energy and environment scenario, it is imperative to develop energy efficient routes for chemical manufacturing that also pave the way for mitigation of greenhouse gas emissions. This work presents an efficient pathway for continuous syngas production via a chemical looping conversion of the two most potent greenhouse gases—CH 4 , and CO 2 . The well-known dry-reforming process of converting CH 4 , and CO 2 to syngas is energy-intensive and suffers from catalyst deactivation. The chemical looping approach, on the other hand, provides avenues for mitigating catalyst deactivation and enabling improved energy efficiency. The key to such process enhancements lies in the intricate structure–function relationships of the catalyst and its correlation to the process variables. We present the reduction and oxidation characteristics of 5 wt.% Ni/Ce 1-x Zr x O 2 -based catalysts (x = 0, 0.4, and 0.625). We demonstrate low temperature CH4 activation over Ni-promoted samples as opposed to pure Ce 1-x Zr x O 2 . Moreover, our results depict an optimum regeneration of these catalysts when oxidized by CO 2 , and H 2 O, which allows for chemical looping operation of steam reforming of methane as well. Process variables were tuned to optimize the CH 4 conversion (over 80%), and H 2 /CO ratio at 650 °C. The critical surface reactions—carbon accumulation and gasification, and thermocatalytic CO 2 splitting were investigated to elucidate the dynamic nature of the catalyst surface. In conclusion, the impact of this work lies in showcasing the opportunities to design chemical looping reactors for energy efficient syngas production from waste greenhouse gases.

25 ENERGY STORAGE↗

The Influence of Shell Mold Composition on the As-cast Macro- and Micro-structure of Thin-Walled IN713C Superalloy Castings

In the investment casting process, the building of ceramic layers around the wax pattern is the main time-consuming stage. Increasing their number ensures sufficient mechanical properties, but also lengthens the whole process, including drying time and preheating of the mold. Four molds for casting Ni-based superalloy IN713C were strengthened by glass fibers, included in the slurry, and metal powder, of Al, Cu, Fe or Ni, in the coverage. Castings were subjected to microstructural investigations in order to find out if the new design can be promising for the manufacture of jet engine components. Bend tests revealed that the green strengths of all new molds were higher, at least 3.65 MPa, than that of the unmodified molds, 3.0 MPa. Optical microscopy revealed that the composition of a mold had a strong influence on stereological parameters of equiaxed IN713C grains. Microstructural observation and hardness measurements of castings revealed differences in the volume fraction of strengthening phases, porosity and hardness. The microstructure due to the complex chemical composition of IN713C consisted of several phases including ternary eutectics as a consequence of L → γ + Ni{sub 7}Zr{sub 2} + (Nb, Zr)C.

36 MATERIALS SCIENCE↗

Optimization of catholyte for halide-based all-solid-state batteries

Halide solid electrolytes gain significant attention due to their high ionic conductivity, low processing temperature, dry air compatibility, and high-voltage stability. However, low cathode active material (CAM) loading in the composite cathode constrains the realization of high energy density for halide-based all-solid-state batteries. In this study, three halide materials, raw Li 3 YBrCl 5 (LYBC-R, <30μm), milled LYBC (LYBC-M, <5 μm) and freeze-dried Li 3 InCl 6 (LIC, <500 nm), were used as catholytes, combined with LYBC-M as the electrolyte and LiIn alloy as the anode. The CAM:catholyte ratio was investigated as well as stack pressure and operating temperature. Our study demonstrates that particle size of the catholyte plays an important role only for high CAM loading or high C-rate cycling. At moderate CAM loading (65 and 70wt% LiNi 0.83 Mn 0.06 Co 0.11 O 2 ) and 0.1 C-rate, all the three catholytes perform well, providing initial discharge capacities >177 mAh/g. At high CAM loading (85wt%) and 0.1 C-rate, a cathode with the nano-scale LIC catholyte provides discharge capacity of 175 mAh/g, while the larger particle size catholytes suffer significantly reduced capacity. Both LYBC and LIC catholytes provided capacity retention >80% after 200 cycles at 0.5C. These results imply that cathode particle size is critically important for performance at high CAM loading. Furthermore, both electrolyte and cathode were tape cast to scale up size and prepare realistic layer thicknesses. A small amount of binder was used in both layers, to balance the electrochemical performance and mechanical properties. Further, the discharge capacity of a tape cell was 152mA h/g at 0.1C with a capacity retention of 81.8% after 20 cycles at 0.5C. The results demonstrate the excellent performance of LYBC as an electrolyte, and provide guidance for halide-based cathode design.

25 ENERGY STORAGE↗

Towards sustainable production and utilization of plant-biomass-based nanomaterials: a review and analysis of recent developments

Abstract Plant-biomass-based nanomaterials have attracted great interest recently for their potential to replace petroleum-sourced polymeric materials for sustained economic development. However, challenges associated with sustainable production of lignocellulosic nanoscale polymeric materials (NPMs) need to be addressed. Producing materials from lignocellulosic biomass is a value-added proposition compared with fuel-centric approach. This report focuses on recent progress made in understanding NPMs—specifically lignin nanoparticles (LNPs) and cellulosic nanomaterials (CNMs)—and their sustainable production. Special attention is focused on understanding key issues in nano-level deconstruction of cell walls and utilization of key properties of the resultant NPMs to allow flexibility in production to promote sustainability. Specifically, suitable processes for producing LNPs and their potential for scaled-up production, along with the resultant LNP properties and prospective applications, are discussed. In the case of CNMs, terminologies such as cellulose nanocrystals (CNCs) and cellulose nanofibrils (CNFs) used in the literature are examined. The term cellulose nano-whiskers (CNWs) is used here to describe a class of CNMs that has a morphology similar to CNCs but without specifying its crystallinity, because most applications of CNCs do not need its crystalline characteristic. Additionally, progress in enzymatic processing and drying of NPMs is also summarized. Finally, the report provides some perspective of future research that is likely to result in commercialization of plant-based NPMs.

09 BIOMASS FUELS↗

Dry etching of epitaxial InGaAs/InAlAs/InAlGaAs structures for fabrication of photonic integrated circuits

A dry etching process to transfer the pattern of a photonic integrated circuit design for high-speed laser communications is described. The laser stack under consideration is a 3.2-µm-thick InGaAs/InAlAs/InAlGaAs epitaxial structure grown by molecular beam epitaxy. The etching was performed using Cl2-based inductively-coupled-plasma and reactive-ion-etching (ICP-RIE) reactors. Four different recipes are presented in two similar ICP-RIE reactors, with special attention paid to the etched features formed with various hard mask compositions, in-situ passivations, and process temperatures. The results indicate that it is possible to produce high-aspect-ratio features with sub-micron separation on this multilayer structure. Additionally, the results of the etching highlight the tradeoffs involved with the corresponding recipes.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Reaction System Design for NO 2 Oxidation of Used Nuclear Fuel for the FY17 Hot Test

A dry pretreatment process based on the oxidation of used nuclear fuel to convert it to a fine powder is being studied for the removal and capture of tritium and iodine before subsequent processing. The process converts oxide fuel into a fine powder at low temperature using NO 2 /O 2 mixtures. The form of the powder product can be selected to be U 3 O 8 , UO 3 , or a nitrate by adjusting the processing conditions. All the fundamental tenets of the process have been successfully demonstrated as a proof of principle, and many aspects have been corroborated multiple times at laboratory scale. The present thrust is to develop the process to a technology-readiness level sufficient to evaluate and estimate the cost of an engineering-scale implementation. A previous roadmap analysis of the implementation determined that the most desirable approach would be based on kilogram-scale experiments using real fuel in parallel with multi-kg testing of prototype systems using surrogate material. Following the planned approach, kilogram-scale experiments will be conducted in FY 2017. This report describes the primary reaction system designs and the equipment that has been fabricated. Details related to instrumentation, data acquisition, and controls have been previously reported.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗