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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.
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Integration of renewables-assisted carbon capture with existing fossil power plants is an economical grid decarbonization technique and renewable intermittency solution.
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The feasibility of an ultra-low energy nuclear-recoil measurement in liquid xenon using neutron capture is investigated for a small (sub-kilogram) liquid xenon detector that is optimized for a high scintillation gain, and a pulsed neutron source. Further, the measurement uses the recoil energies imparted to xenon nuclei during the de-excitation process following neutron capture, where promptly emitted γ cascades can provide the nuclei with up to 0.3 keV nr of recoil energy due to conservation of momentum. A successful calibration of scintillation photon and ionization electron yields below this energy will contribute to a greater sensitivity for liquid xenon experiments in searches for light WIMPs.
The presentation provides details on the research work done by the CCSI2 team on techno-economic modeling and optimization of an MEA solvent-based carbon capture system connected to a large scale NGCC power plant, at high CO2 capture levels above 90%. This includes an overview of the process and economic models along with the optimization results.
Converting captured CO₂ into fuels and marketable chemicals using bifunctional materials (BFMs) represents a promising sustainable solution. In this study, a BFM composed of a Cr₂O₃/ZSM-5 catalyst and a CaO-CaZrO₃ sorbent was developed and tested for the integrated CO₂-oxidative dehydrogenation of propane (CO₂-ODHP) in a fixed bed reactor. The CaO-CaZrO₃ sorbent, prepared using the citrate sol-gel method, demonstrated high CO₂ adsorption capacity and improved cyclic stability compared to pure CaO. The BFM achieved 23.5% propane conversion, 52.5% propylene selectivity, and 68.7% olefin selectivity at isothermal adsorption-reaction conditions (630-630 °C). Overall, this study provides insights into enhancing CO2 adsorption and developing materials for integrated CO2 capture and conversion.
The development of the polyvinylidene fluoride (PVDF) dust detector for space missions--such as the Halley Comet Missions where the impact velocity was very high as well as for missions where the impact velocity is low was extended to include: (1) the capability for impact position determination - i.e., x,y coordinate of impact; and (2) the capability for particle velocity determination using two thin PVDF sensors spaced a given distance apart - i.e., by time-of-flight. These developments have led to space flight instrumentation for recovery-type missions, which will measure the masses (sizes), fluxes and trajectories of incoming dust particles and will capture the dust material in a form suitable for later Earth-based laboratory measurements. These laboratory measurements would determine the elemental, isotopic and mineralogical properties of the captured dust and relate these to possible sources of the dust material (i.e., comets, asteroids), using the trajectory information. The instrumentation described here has the unique advantages of providing both orbital characteristics and physical and chemical properties--as well as possible origin--of incoming dust.
A Brønsted acid-base reaction based method was employed to tether alkylamine into Cr-MIL-101-SO 3 H for CO 2 capture. A systematic optimization of the amine tethering process was also conducted to maximize the CO 2 uptake of the modified MOF. Under the optimal amine tethering condition, the obtained TAEA functionalized Cr-MIL-101-SO 3 H (Cr-MIL-101-SO 3 H-TAEA, TAEA = Tris(2-aminoethyl)amine) has cyclic CO 2 uptakes of 2.28 mmol/g -1 at 150 mbar and 40 °C, and 1.12 mmol/g -1 at 0.4 mbar and 20 °C. The low-cost starting materials and simple synthetic procedure of Cr-MIL-101-SO 3 H-TAEA all promise its advantages in large-scale production in practical applications.
The encapsulation of highly viscous liquid-like Nanoparticle Organic Hybrid Materials (NOHMs) inside a gas permeable polymer to form SIPs (Solvent Impregnated Polymers) significantly enhanced the CO 2 capture kinetics of NOHMs, leading to a remarkable 50-fold increase in CO 2 flux compared to the neat NOHMs. To understand the mechanism for enhanced CO 2 mass transfer within these hybrid materials, kinetic modeling of CO 2 uptake into SIPs containing polyethylenimine functionalized NOHMs, denoted NPEI-SIP, was conducted. CO 2 mass transfer into NPEI-SIP films was found to conform, both qualitatively and quantitatively, with a diffusion-controlled moving front model. The diffusion-controlled model was also used to simulate CO 2 uptake within a fixed bed containing polydisperse NPEI-SIP particles, and this model accurately predicted experimentally measured breakthrough curves at 25 °C and 50 °C. The 50-fold increase in gas flux was shown to be a consequence of the very large CO 2 permeability within the polymer–solvent composite. Furthermore, the increase in gas flux is also dependent on the diffusion–reaction regime in which the chemical solvent operates, and the largest improvement will occur when immobilizing solvents, such as NOHMs, which operate in the instantaneous-reaction regime. The CO 2 capacity (~3 mol CO 2 /kg) and saturation time (~5 min) of 430 μm SIP particles were comparable to popular CO 2 chemisorption materials such as amine grafted silicates, in spite of the slow kinetics of NOHM-I-PEI in liquid form (CO 2 saturation time ~24 h for a 1 mm thin film).
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Presented by NETL at IEAGHG 5th Post Combustion Capture Conference, 09/17
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To understand the effect of porous parameters and chemical components on CO 2 capturing performance of solid state amine absorbents and their kinetic parameters, a clay mineral-based CO 2 absorbent was prepared by impregnating five different liquid amines onto SiO 2 nanowire clusters from fibrous sepiolite (Sep). Characterization was conducted by XRD, SEM, FTIR, and N 2 adsorption–desorption isotherm, CO 2 adsorption performances were measured by TGA. After acid treatment, the raw Sep mineral changed into amorphous silica nanowires, and the largest S BET of the obtained SiO 2 nanowires reached 320 m 2 /g, which was 8 times larger than the pristine mineral. Amongst the adapted amines, tetraethylenepentamine (TEPA) showed superiority in the CO 2 adsorption capacity. The optimized adsorption capacity reached 3.7 mmol/g at 75 °C from a CO 2 + N 2 mixture on a ~50 wt% TEPA loaded SiO 2 sample, and the capacity remained 3.6 mmol/g after ten circles of adsorption/desorption tests. The pore size and pore structure of the matrix, rather than the surface area, will obviously affect the adsorption ability of the product. Kinetic parameters for the CO 2 adsorption process fitted well with a fractional-order model, confirming that the CO 2 adsorption process by the solid absorbent should be a combination of both physical and chemical reactions. Results in this article provide detailed parameters for preparing and understanding these clay mineral based solid state CO 2 absorbents.
In this perspective, we detail how solvent-based carbon capture integrated with conversion can be an important element in a net-zero emission economy.
Here, we report the first observation of the parity-violating gamma-ray asymmetry 𝐴$^{𝑛𝑝}_{𝛾}$ in neutron-proton capture using polarized cold neutrons incident on a liquid parahydrogen target at the Spallation Neutron Source at Oak Ridge National Laboratory. 𝐴$^{𝑛𝑝}_{𝛾}$ isolates the Δ𝐼 =1, 3 𝑆 1 → 3 𝑃 1 component of the weak nucleon-nucleon interaction, which is dominated by pion exchange and can be directly related to a single coupling constant in either the DDH meson exchange model or pionless effective field theory. We measured 𝐴$^{𝑛𝑝}_{𝛾}$=[−3.0±1.4(stat)±0.2(syst)]×10 −8 , which implies a DDH weak 𝜋𝑁𝑁 coupling of ℎ$^1_𝜋$=[2.6±1.2(stat)±0.2(syst)]×10 −7 and a pionless EFT constant of 𝐶 3 𝑆 1 → 3 𝑃 1 /𝐶 0 =[−7.4±3.5(stat)±0.5(syst)]×10 −11 MeV −1 . We describe the experiment, data analysis, systematic uncertainties, and implications of the result.