An influence coefficient method for the prediction of longitudinal stability derivatives of rigid and elastic airplanes.
Longitudinal stability derivatives prediction for rigid and elastic airplanes, using influence coefficient method
Dusto, A.↗
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Upgrading Fast Pyrolysis Liquids
The liquid formed by the fast pyrolysis (FP) of biomass is commonly termed bio-oil. Biomass is converted to bio-oil through FP at 400-550°C typically at 1 atm. During FP, the biomass is held at temperature for a residence time on the order of 1-2 seconds. FP is beneficial from the standpoint that a large portion of the total mass and carbon contained in the biomass is converted and retained in the liquid bio-oil fraction. However, bio-oil is acidic, viscous, and thermally unstable. Bio-oil must be upgraded in order to be considered as a liquid transportation fuel or separated and further treated to produce value-added chemicals. Bio-oil is generally regarded as difficult to upgrade due to its thermal instability and chemical complexity which is derived in part from the incorporation of highly reactive species such as aldehydes and terminal olefins as well as the presence of sugars and anhydrosugar species which undergo secondary polymerization reactions when heated. Upgrading strategies considered in this chapter include methods to stabilize and deoxygenate bio-oil through low temperature hydroprocessing to stabilize bio-oil followed by higher temperature “deep hydrotreating” to remove the majority of oxygen present; converting bio-oil catalytically (often with zeolites such as HZSM-5) prior to condensation with catalysts inside the FP reactor or in a separate fixed or fluidized bed after the FP reactor; catalytic cracking with acid catalysts such as zeolites after condensation; or through physical or chemical separations to improve bio-oil stability, extract valuable chemicals, or produce H¬2. Bio-oil upgrading by co-processing with refinery streams such as vacuum gas oil in a fluid catalytic cracking (FCC) unit in a refinery has also been investigated. Numerous excellent reviews, perspectives and other chapters have been published in the preceding 7 years.[1-10] Reviews specific to individual sections within this chapter are at the beginning of the individual sections. This chapter is intended as an update to the original article authored by Prof. Anthony V. Bridgwater, Thermochemical Processing of Biomass: Conversion into Fuels, Chemicals and Power, First Edition, Edited by Robert C. Brown, © 2011 John Wiley & Sons, Ltd. We gratefully acknowledge the original contribution by Prof. Bridgwater and have kept much of his original discussions intact with updated references. The scope of this updated chapter includes references published since about 2010. In the interest of space many of the original references included in the original version were not included. Thus, Prof. Bridgwater’s original chapter should be viewed as a companion to this updated chapter to provide a holistic set of references to the numerous bio-oil upgrading processes discussed herein.
Albrecht, Karl O.↗
Advances and Challenges in Low‐Temperature Upcycling of Waste Polyolefins via Tandem Catalysis
Abstract Polyolefin waste is the largest polymer waste stream that could potentially serve as an advantageous hydrocarbon feedstock. Upcycling polyolefins poses significant challenges due to their inherent kinetic and thermodynamic stability. Traditional methods, such as thermal and catalytic cracking, are straightforward but require temperatures exceeding 400 °C for complete conversion because of thermodynamic constraints. We summarize and critically compare recent advances in upgrading spent polyolefins and model reactants via kinetic (and thermodynamic) coupling of the endothermic C─C bond cleavage of polyolefins with exothermic reactions including hydrogenation, hydrogenolysis, metathesis, cyclization, oxidation, and alkylation. These approaches enable complete conversion to desired products at low temperatures (<300 °C). The goal is to identify challenges and possible pathways for catalytic conversions that minimize energy and carbon footprints.
Zhang, Wei [State Key Laboratory of Petroleum Mole↗
Advances and Challenges in Low‐Temperature Upcycling of Waste Polyolefins via Tandem Catalysis
Abstract Polyolefin waste is the largest polymer waste stream that could potentially serve as an advantageous hydrocarbon feedstock. Upcycling polyolefins poses significant challenges due to their inherent kinetic and thermodynamic stability. Traditional methods, such as thermal and catalytic cracking, are straightforward but require temperatures exceeding 400 °C for complete conversion because of thermodynamic constraints. We summarize and critically compare recent advances in upgrading spent polyolefins and model reactants via kinetic (and thermodynamic) coupling of the endothermic C─C bond cleavage of polyolefins with exothermic reactions including hydrogenation, hydrogenolysis, metathesis, cyclization, oxidation, and alkylation. These approaches enable complete conversion to desired products at low temperatures (<300 °C). The goal is to identify challenges and possible pathways for catalytic conversions that minimize energy and carbon footprints.
C-C cleavage↗
Influence of Magnetite Nanoparticles and Quantum Dots on the Expression of Reference Genes in Peripheral Blood Cells
We studied the influence of magnetite nanoparticles (FeO•Fe{sub 2}O{sub 3}) and quantum dots (CdSe/ZnS coated with mercaptopropionic acid) on the expression of 5 common reference genes (BA, B2M, PPIA, UBC, and YWHAZ) in peripheral blood cells from 20 volunteers by reverse transcription PCR method. The stability of the expression of reference genes varied depending of the cells type and chemical structure of nanoparticles. The level of YWHAZ mRNA after exposure by nanoparticles demonstrated highest stability in lymphocytes, neutrophils, and monocytes. Stability of YWHAZ expression was confirmed by Western blotting. Our findings suggest that YWHAZ is the most suitable as the reference gene.
60 APPLIED LIFE SCIENCES↗
Experimental Protocols for Studying Organic Non-aqueous Redox Flow Batteries
We report that Redox flow batteries (RFBs) are promising devices for grid-scale energy storage due to the decoupling of power and energy, which can be independently scaled by the electrode area and storage tank size, respectively. To date, only aqueous RFBs, such as the vanadium RFB, have been implemented commercially. Nevertheless, the limited energy densities and high-cost materials may preclude their wider market penetration. Organic non-aqueous redox-flow batteries (O-NRFBs), which utilize redox-active organic molecules (ROMs), have been offered as an attractive alternative. Many possible advantages include the use of earth-abundant elements (C, H, N, O, S, F), wherein the ROMs can be prepared from low-cost and sustainable materials. Additionally, a large variety of electroactive moieties are accessible as building blocks, providing a synthetic platform to tune the properties of ROMs through rational design. As a consequence, the development of novel ROMs has attracted researchers with diverse backgrounds, prompting remarkable innovations in the past decade. However, consistency in experimental protocols (e.g., electrochemical methods, cycling stability, experimental conditions) has not coincided with this uptick in research, leading to sometimes ambiguous and incomparable results. This is further convoluted by the complexity innate to battery development, such as cell design, detection, and characterization of reactions and active components. The O-NRFB application imposes stringent requirements on the physical or/and chemical processes involved in electrochemical cycling. Yet such considerations are often overlooked. Further, while quantum mechanical calculations provide a convenient tool for evaluating and selecting ROM candidates, this simulation is not always performed. Thus, in this Energy Focus, we detail a means to standardize experimental protocols for studies of O-NRFBs and suggest practices to facilitate fundamental understanding and development of ROMs.
25 ENERGY STORAGE↗
Scaling Behavior of Thermally Driven Fractures in Deep Low‐Permeability Formations: A Plane Strain Model With 1‐D Heat Conduction
Abstract Injection of cold fluids through/into deep formations may cause significant cooling, thermal stress, and possible thermal fracturing. In this study, the thermal fracturing of low‐permeability formations under one‐dimensional heat conduction was investigated using a plane strain model. Dimensionless governing equations, with dimensionless fracture length , aperture , spacing , time , and effective confining stress , were derived. Solution of single thermal fracture was derived analytically, while solution of multiple fractures with constant (or dynamic) spacing were obtained using the displacement discontinuity method (and stability analysis). For single fracture, increases nonlinearly with and then transitions to scaling law , indicating that late‐time fracture length increases linearly with the square root of cooling time. For constantly spaced fractures, deviates from the single‐fracture solution at a later for a larger , showing slower propagation under inter‐fracture stress interaction . For dynamically spaced fractures, fracture arrest induced by stress interaction was determined by the stability analysis; the fully transient solution provides evolution of dimensionless fracture length, spacing, aperture, and pattern; a similar scaling law, with , obtained shows the effect of both stress interaction and fracture arrest. The solution and scaling law provide fast predictions for all reservoir and cooling conditions using (single) model parameter . Application to a geothermal site with demonstrates that thermal fractures reach 0.67, 6.25, and 78.00 m in length, 0.49, 2.30, and 13.00 m in spacing, and 0.43, 2.09, and 12.19 mm in aperture at 1, 100, and 10,000 days.
Chen, Bin↗
Ineffectiveness of formamidine in suppressing ultralow thermal conductivity in cubic hybrid perovskite FAPbI 3
Understanding lattice dynamics and thermal transport mechanisms in cubic hybrid organic–inorganic perovskites remain challenging due to strong anharmonicity and phase transitions. Here, we investigate the thermal transport behavior in benchmark cubic hybrid perovskite FAPbI 3 by coupling first principles-based anharmonic lattice dynamics with a linearized Wigner transport equation. Using the Temperature-Dependent Effective Potential (TDEP) method, we stabilize the negative soft modes, primarily dominated by organic FA + cations. Our calculations predict an ultra-low thermal conductivity of ~$0.63\,{\rm{W}}{{\rm{m}}}^{-1}{{\rm{K}}}^{-1}$ at 300 K, following a temperature dependence of T −0.740 . Contrary to common assumptions, we find that the [PbI 3 ] 1- units, rather than FA + cations, dominate thermal resistance. Furthermore, we demonstrate that anharmonic force constants are highly temperature-sensitive, relying on 0-K force constants significantly underestimates thermal conductivity. Our study not only elucidates the microscopic mechanisms governing thermal transport in FAPbI 3 but also provides a robust framework for modeling heat conduction in hybrid organic-inorganic compounds.
Zheng, Jiongzhi [Dartmouth College, Hanover, NH (U↗
Mechanisms of alumina growth via atomic layer deposition on nickel oxide and metallic nickel surfaces
We aim at elucidating the mechanism of the trimethyl aluminum (TMA) decomposition on oxidized nickel (NiO) and metallic nickel (Ni) facets in the absence of a source of hydroxyl groups. This TMA decomposition mechanism constitutes the earliest stage of growth of Al 2 O 3 coatings with the atomic layer decomposition (ALD) method, which stabilizes nickel catalysts in energy-intensive processes such as the dry reforming of methane. Our first-principles calculations suggest thermodynamic favorability for the TMA decomposition on metallic nickel compared to oxidized nickel. Moreover, the decomposition of TMA on metallic nickel showed almost no differences in terms of energy barriers between flat and stepped surfaces. Regarding the impact of the CH 3 radicals formed after TMA decomposition, we calculated stronger adsorption on metallic nickel facets than on oxidized nickel, and these adsorption energies are comparable to the adsorption energies calculated in earlier works on Al 2 O 3 ALD growth on palladium surfaces. These results lead us to believe in the growth of porous Al 2 O 3 coatings triggered by CH 3 contamination rather than due to preferential TMA decomposition on stepped and/or defective facets. The CH 3 radicals are likely to be thermally stable at temperatures used during Al 2 O 3 ALD processes, partially passivating the surface towards further TMA decomposition.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Two-dimensional perovskite heterostructures for single crystal semiconductor devices
Two-dimensional (2D) perovskites have gained much attention lately owing to their excellent optoelectronic properties, chemical tunability, and environmental stability. Multiple methods have been devised to synthesize high quality 2D perovskite single crystals, and recent progress in fabricating its heterostructures is notable as well. In particular, with growing interest in 2D van der Waals heterostructures, 2D perovskites have become a strong candidate as a new building block for heterostructures to reveal unique physical properties across different interfaces. Until now, various heterostructure devices of 2D perovskite single crystals with other types of 2D materials such as transition metal dichalcogenides (TMDs) and graphene have been studied, which have shown intriguing results including interlayer excitons and enhanced electronic properties. Here, we introduce various synthetic approaches to realize 2D perovskite single crystals and unique characteristics of their single crystal heterostructures fabricated with precision, possessing sharp interfaces. Moreover, recent studies of semiconductor devices based on 2D perovskite single crystal heterostructures are discussed in-depth. New perspectives to further the horizon in the field of 2D perovskite heterostructures are suggested in this work including the consideration of metal–2D material van der Waals contact, application of dry transfer techniques, electric bias driven ion diffusion studies, and nanocrystal array fabrication. 2D perovskite heterostructure single crystal devices factoring in these novel perspectives will further uncover the true potential of these materials for highly efficient and stable semiconductor devices.
Physics↗
Convert Widespread Paraelectric Perovskite to Ferroelectrics
While nature provides a plethora of perovskite materials, only a few exhibit large ferroelectricity and possibly multiferroicity. The majority of perovskite materials have the nonpolar CaTiO 3 (CTO) structure, limiting the scope of their applications. Based on the effective Hamiltonian model as well as first-principles calculations, we propose a general thin-film design method to stabilize the functional BiFeO 3 (BFO)- type structure, which is a common metastable structure in widespread CTO-type perovskite oxides. It is found that the improper antiferroelectricity in CTO-type perovskite and ferroelectricity in BFO-type perovskite have distinct dependences on mechanical and electric boundary conditions, both of which involve oxygen octahedral rotation and tilt. Thus the above difference can be used to stabilize the highly polar BFO-type structure in many CTO-type perovskite materials.
71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
Presentation: Bench Scale Development of a Novel Direct Air Capture Technology Using High-Capacity Structured Sorbents
The presentation provides a status report of bench-scale development of a DAC technology, specifically sorbent washcoat optimization, sorbent stability, desorption method optimization, heating layer performance, and bench-scale design & testing.
Gupta, Raghubir↗
Differential inequalities and extension of lyapunov's method.
Liapunov method and stability and boundedness of solutions of differential inequalities
LIAPUNOV FUNCTION↗
Liapunov's second method.
Liapunov second method and stability theory of autonomous and certain nonautonomous systems
LIAPUNOV FUNCTION↗
Stability of continuous systems.
Stability of motion of continuous dynamical systems analyzed via computing machines
SYSTEM STABILITY↗