Energy Change Research Articles

In-Situ structural and Adsorbate Induced Surface Evolutions Monitored By Electrochemical Stress Measurements

We report on in-situ electrochemical stress measurements of well-defined surfaces during electrochemical reactions in aqueous media. Electrochemical stress measurements during hydrogen evolution reaction (HER) on Pt surfaces shows distinct pH-dependent features which we assign to anion adsorption/desorption and hydrogen adsorption/desorption. Our surface stress analysis shows higher hydrogen induced stresses at alkaline environments than stresses observed at acidic pHs. This observation is consistent with the monotonic change in apparent hydrogen binding energy with pH, most likely due to the changes in water interactions with surface. However, H-induced surface stress shows a dramatic increase around neutral pH. We will present our analysis of how interfacial water may explain this effect. Additionally, we will show how in-situ underpotential deposition of Cu on Pt and Ni on Au changes Had induced effects on these surfaces.We will also discuss the structural and compositional evolution of Sr2Fe2O6-δ thin films during oxygen evolution reaction (OER). Interestingly, in-situ electrochemical stress measurements show a tensile stress response during OER which is different from Au model surfaces. We will present our analysis of how potential controlled formation of iron (oxy)hydorxides may explain in-situ stress response and structural evolution of perovskite type structures during OER.In summary, our analysis shows how adsorbate-induced effects can be used to explain surface reactions, and particularly explain and provide insight into interfacial structural changes and water interactions at different pHs.

Improvements in Long-Term Durability of CO2 Electrolyzer Producing Formate Designed for Integration with Solar Cells for Artificial Photosynthesis

Artificial photosynthetic cells have been extensively studied for carbon neutrality, yet in lab-scale. We have previously constructed practically large-sized cells consisting of CO2 electrolyzers and crystalline silicon solar cells.1,2 Our CO2 electrolyzers adopt a facing cathode-anode configuration, using a Ru complex polymer (RuCP) catalyst realizing a low overpotential for CO2 reduction and an IrO x -based catalyst with a high catalytic activity for water oxidation.3 1000 cm2-sized cells achieved a solar-to-chemical energy-conversion efficiency (η STC) of 7.2%,1 and a further scaled-up 1 m2-cell demonstrated a higher η STC of 10.5%, yielding a large formate production rate of 1.2 mol/h.2 In the present study, we improved the long-term durability of the CO2 electrolyzer. We prepared the 75 cm2-sized CO2 electrolyzer using the improved cathode and the anode, and achieved high formate Faradaic efficiencies (FE) exceeding 80% and electricity-to-chemical energy-conversion efficiencies (η ETC) of around 60% even after 3000 h operation under practical conditions, as shown in Fig. 1.In the previous large-sized cells, the operating current gradually decreased during continuous operation within dozen of hours. We investigated the causes of the degradation and identified three key factors. Two of these factors were associated with the cathode electrodes: detachment of the RuCP catalyst from the carbon supports and peeling off of the carbon supports from the conducting Ti substrates. An introduction of a pyrrole derivative containing amino group in the RuCP, coupled with an application of a UV-ozone treatment to create carboxyl groups on the carbon supports, effectively reduced the detachment of the RuCP catalyst by forming strong chemical bonds. A newly-developed chemically-resistant graphite adhesive composed of graphite particles and a polyvinylidene fluoride (PVDF) binder prevented the carbon supports from peeling off from the Ti-plates. The post-loading process of the RuCP, i.e., RuCP-loading on the carbon supports already-bonded on the Ti-plates using the new adhesive eliminated the detrimental impact of the heat treatment for curing the adhesive. The third factor involved detachment of the anode catalyst of IrO x particles from the Ti-plates.4 Therefore, we replaced the IrO x anodes with highly durable counterparts comprising IrO x -TaO x /Pt-Metal oxide/Ti-plates.Another critical issue we addressed was the validity of laboratory-based evaluations for reflecting outdoor operations. In our previous study, we vertically installed the integrated CO2 electrolyzers and solar cells on the ground and evaluated their performance under continuous simulated sunlight (ca. 1 sun).2,3 This vertical setup was chosen to prevent a decrease in η STC caused by crossover reactions that would occur when the electrolyzers are inclined. Indeed, it has been reported that oxygen reduction reaction (ORR) of the O2 bubbles generated at the anode and transferred to the cathode can be substantial in a single-chamber water-splitting reactor.5 By contrast, although the present CO2 electrolyzer was installed at an inclined angle of 30 °, which is approximately the optimal value for receiving more solar energy, the crossover reactions were well-suppressed because the porous separator film inserted between the facing cathode and anode impeded the transfer of O2 bubbles from the anode to the cathode. However, the use of a separator film raised another issue: the O2 bubbles trapped on the film narrowed the effective film area. Intermittent operation corresponding to changes in solar energy during the day mitigates the detrimental impact of the second issue.Thus, we established the groundwork for the widespread use of integrated CO2 electrolyzers and solar cells for artificial photosynthesis, demonstrating high durability, exceptional FE, and η ETC.References N. Kato, et al., A large-Sized Cell for Solar-Driven CO2 Conversion with a Solar-to-Formate Conversion Efficiency of 7.2%, Joule, (2021) 5, 687.N. Kato, et al., Solar Fuel Production from CO2 using 1 m-square-sized Reactor with a Solar-to-Formate Conversion Efficiency of 10.5%, ACS Sustain. Chem. Eng.,(2021) 9, 16031.T. Arai, S. Sato, T. Morikawa, A Monolithic Device for CO2 Photoreduction to Generate Liquid Organic Substances in a Single-Compartment Reactor, Energy Environ. Sci., (2015) 8, 1998.M. Shiozawa, et al., Improved Durability of Highly Active IrO x Electrodes for Electrocatalytic Oxygen Evolution Reaction, Electrocatalysis, (2022) 13, 830.K. Obata, et al., Multiphase Fluid Dynamics Simulations of Product Crossover in Solar-driven, Membrane-less Water Splitting, Cell Rep. Phys. Sci, (2021) 2, 100358. Figure 1

Energy Changing Paths for Li-Ion Batteries Under Nonequilibrium Process

It has been discovered that the electrodes of Li-ion batteries have abnormal phase transition phenomena during nonequilibrium process. As a two-phase-coexistence material, LiFePO4 (LFP) shows single phase during both high-rate lithiation and delithiation. Furthermore, a far from equilibrium state results in LFP particles with meta-stable amorphous structures and layered oxides exhibiting two-phase-coexistence during high rate delithiation. It is well known that a stable single-phase structure is an important characteristic for the electrodes with better high-rate performance, since the energy barriers of nucleation and growth for new phases are eliminated. Understanding the mechanisms of the abnormal phase transition during nonequilibrium process is therefore essential for designing the electrodes with fast (dis)charging. In this work, we model the free energy of electrodes with a series of order parameters based on nonequilibrium thermodynamics and continuum mechanics. Developed governing equations for the kinetics of the order parameters reveal the mechanism of the abnormal phase transitions for LFP and layered oxides under high rate (de)lithiation. The generation of dislocations is cross-coupled with the chemical reaction of Li-ion on the surface of electrode particles. Such coupling is the origin of materials choosing various energy changing paths under different (dis)charging conditions and resulting in various lattice parameters and structures. The dislocation density is the key parameter for the path selection since it alters dislocation-induced energy. In the simulations for LFP and layered oxides, the changes of order parameters agree with the abnormal phase transition observed in existing experimental studies. Our study indicates a potential strategy of introducing dislocations with surface engineering for optimizing the (dis)charging path of electrode materials to obtain stable single-phase characteristics and promote the kinetic capability.

Coal deformation characteristics during methane displacement by pulsed nitrogen injection: New method of using pulsed energy to improve coal permeability

The displacement of methane by injecting nitrogen is an effective method for improving extraction efficiency in low-permeability coal seams. By conducting the experiments on uniform/pulsed pressure nitrogen injection for methane displacement (UPNI-MD/PPNI-MD), the coal deformation characteristics are quantitatively characterized, and the coal deformation mechanism is discussed. The results show that the technology of methane displacement by PPNI-MD is more effective in enhancing the permeability of low-permeability coal seams. The pressure of nitrogen injection and the amount of methane/nitrogen adsorption are crucial factors affecting the coal deformation during the process of UPNI-MD/PPNI-MD. The erosive effect of methane adsorption on the mechanical properties of coal decreases, while the erosive effect of nitrogen adsorption on the mechanical properties of coal shows a “wave-like” variation in the case of PPNI-MD. The application of PPNI-MD technology can effectively decrease the coal expansion deformation while undergoing the methane displacement process. Nitrogen injection to displace methane breaks the system energy balance of coal, resulting in deformation. And the coal deformation during nitrogen injection for methane displacement depends on the energy carried by the injected nitrogen, the energy change during gas competitive adsorption and the heat exchange between nitrogen and coal. The effective stress of coal depends on the change in methane/nitrogen pressure. The mechanical properties of coal depend on the amount of methane/nitrogen adsorption and the pore pressure. High-energy nitrogen damage to coal during the process of PPNI-MD is manifested in coal deformation caused by methane/nitrogen pressure, coal deformation caused by methane/nitrogen adsorption, and damage to coal mechanical properties caused by methane/nitrogen adsorption.

Optimizing Nitrate Reduction to Ammonia via Modulating Adsorption-Desorption Dynamics with High-Entropy CuNiCoZnMn Alloy Catalysts.

NO3RR synthesis of ammonia is a complex eight-electron reaction involving multiple steps and intermediates, in which NO3- adsorption and NH3 desorption are crucial. The Cu-based high entropy quinary alloy catalyst has good surface adsorption and desorption ability for the reduction of nitric acid to ammonia. Here, the catalytic sites were coordinated by constructing CuNiCoZnMn alloys to adjust the electronic structure of the catalytic sites to facilitate the reaction of the substrate and thus optimize the whole reaction path. Based on the ternary alloy CuNiCo, the introduction of the Zn element continues to reduce the desorption energy barrier, and the introduction of the Mn element continues to enhance the initial adsorption energy so that the target product can be quickly held and released to accelerate the production of ammonia. The NH3 yield and Faraday efficiency obtained for the quinary CuNiCoZnMn alloy catalyst reached 723.7 μmol h-1 cm-2 and 96.6%, respectively, at -0.35 V vs RHE potential. The density functional theory calculations showed that the quinary CuNiCoZnMn alloy (NO3- to *NO3-) initial adsorption-free energy change and (*NH3 to NH3) NH3 desorption-free energy change are -2.50, 0.072 eV, respectively, which are significantly better than those of the ternary CuNiC and quaternary CuNiCoZn of -2.02, 0.544 eV and -1.97, 0.217 eV.

Size-Dependent Ab Initio Atomistic Thermodynamics from Cluster to Bulk: Application to Hydration of Titania Nanoparticles.

Ab initio atomistic thermodynamics (AIAT) has become an indispensable tool to estimate Gibbs free energy changes for solid surfaces interacting with gaseous species relative to pressure (p) and temperature (T). For such systems, AIAT assumes that solid vibrational contributions to Gibbs free energy differences cancel out. However, the validity of this assumption is unclear for nanoscale systems. Using hydrated titania nanoparticles (NPs) as an example, we estimate the vibrational contributions to the Gibbs free energy of hydration (ΔGhyd(T,p)) for arbitrary NP size and degree of hydration. Comparing ΔGhyd(T,p) phase diagrams for NPs when considering these contributions (AIATnano) relative to a standard AIAT approach reveals significant qualitative and quantitative differences, which only become negligible for large systems. By constructing a size-dependent ΔGhyd(T,p) phase diagram, we illustrate how our approach can provide deeper insights into how nanosytems interact with their environments, with many potential applications (e.g., catalytic nanoparticles, biological colloids, nanoparticulate pollutants).

Three-dimensional solidification modeling of various materials using the lattice Boltzmann method with an explicit enthalpy equation.

Based on the mesoscopic scale, the lattice Boltzmann method (LBM) with an enthalpy-based model represented in the form of distribution functions is widely used in the liquid-solid phase transition process of energy storage materials due to its direct and relatively accurate characterization of the presence of latent heat of solidification. However, since the enthalpy distribution function itself contains the physical properties of the material, these properties are transferred along with the enthalpy distribution function during the streaming process. This leads to deviations between the enthalpy-based model when simulating the phase transition process of different materials mixed and the actual process. To address this issue, in this paper, we construct an enthalpy-based model for different types of materials. For multiple materials, various forms of enthalpy distribution functions are employed. This method still uses the form of enthalpy distribution functions for collisions and streaming processes among the same type of substance, while for heat transfer between different materials, it avoids the direct transfer of enthalpy distribution functions and instead applies a source term to the enthalpy distribution functions, characterizing the heat transfer between different materials through the energy change before and after mixing based on the temperature. To verify the accuracy of the method proposed in this paper, a detailed solidification model for two different materials is constructed using the example of water droplets solidifying in air, and the results are compared with experimental outcomes. The results of the simulation show that the model constructed in this paper is largely in line with the actual process.

Universal constraints on energy flow and SYK thermalization

We study the dynamics of a quantum system in thermal equilibrium that is suddenly coupled to a bath at a different temperature, a situation inspired by a particular black hole evaporation protocol. We prove a universal positivity bound on the integrated rate of change of the system energy which holds perturbatively in the system-bath coupling. Applied to holographic systems, this bound implies a particular instance of the averaged null energy condition. We also study in detail the particular case of two coupled SYK models in the limit of many fermions using the Schwinger-Keldysh non-equilibrium formalism. We solve the resulting Kadanoff-Baym equations both numerically and analytically in various limits. In particular, by going to low temperature, this setup enables a detailed study of the evaporation of black holes in JT gravity.

Improving Photophysical Properties of Deazaflavin Derivatives by Acrylaldehyde Bridging: A Theoretical Investigation

AbstractThe electronic structure and photophysical properties of several acrylaldehyde‐bridged deazaflavin derivatives (cFLs) were investigated theoretically. The impact of acrylaldehyde bridging on photophysical properties of deazaflavin (cFL) is strongly site‐dependent. Specifically, the change of adiabatic energy of electronic transitions(ΔEad) and vibronic coupling promote fluorescent emission to be comparable to internal conversion of cFL and cFL4 (both C5−C6 and C9−N10 bridged, but C9−N10 bridged by propene), turning them eligible as fluorescent sensors. As El‐Sayed's rule is satisfied in cFL1(C5−C6 bridged), cFL2(C9−N10 bridged) and cFL3(both C5−C6 and C9−N10 bridged), intersystem crossing from first singlet excited state to triplet excited states (Tn) become dominant and the evolution of excited cFLs from T1 appears vital. The rate constants of photophysical processes indicate these cFLs are of dominantly high steady state T1 concentration and are potential triplet sensitizers. We expect the findings would pave the way for rational design of novel cFLs with extraordinary photophysical properties.

Surface Characteristics and Artificial Weathering Resistance of Oil-Based Coatings on the Chemically and Thermally Modified Short-Rotation Teak Wood.

Improving the durability of short-rotation wood can be achieved through chemical and thermal modification. Chemical and thermal modification can have an impact on the physicochemical properties of wood, which can affect wood's surface characteristics and its resistance to weathering. The purpose of this study was to investigate the surface characteristics and artificial weathering resistance of chemically and thermally modified short-rotation teak wood coated with linseed oil (LO)-, tung oil (TO)-, and commercial oil-based coatings consisting of a mixture of linseed oil and tung oil (LT) and commercial oil-based polyurethane resin (LB) coatings. The short-rotation teak woods were prepared in untreated and treated with furfuryl alcohol (FA), thermal treatment (HT) at 150 and 220 °C, and combination of glycerol-maleic anhydride (GMA) impregnation with thermal treatment at 150 and 220 °C. The surface characteristics measured were surface free energy, wettability, Persoz hardness, bonding quality, and color changes before and after artificial weathering exposure. The results showed that chemical and thermal modifications treatment tended to reduce total surface free energy (SFE), hardness, wettability, and bonding quality. FA and GMA at 220 °C treatments provided homogenization effect on surface characteristics, especially in total SFE and wettability. The total SFE of untreated wood ranged from 45.00 to 51.13 mN/m, and treated wood ranged from 40.58 to 50.79 mN/m. The wettability of oil-based coating according to K-value ranged from 0.20 to 0.54. TO presented better photostability than LO. Short-rotation teak wood coated with oil-based commercial coatings presented better weathering resistance compared to pure natural drying oil. Commercial oil-based coatings provided better weathering protection for the chemically and thermally modified teak wood. The application of oil-based coatings on chemically and thermally modified short-rotation teak is being considered for the development of a better wood-protection system.

A novel kinetic model to demonstrate the independent effects of ATP and ADP/Pi concentrations on sarcomere function.

Understanding muscle contraction mechanisms is a standing challenge, and one of the approaches has been to create models of the sarcomere-the basic contractile unit of striated muscle. While these models have been successful in elucidating many aspects of muscle contraction, they fall short in explaining the energetics of functional phenomena, such as rigor, and in particular, their dependence on the concentrations of the biomolecules involved in the cross-bridge cycle. Our hypothesis posits that the stochastic time delay between ATP adsorption and ADP/Pi release in the cross-bridge cycle necessitates a modeling approach where the rates of these two reaction steps are controlled by two independent parts of the total free energy change of the hydrolysis reaction. To test this hypothesis, we built a two-filament, stochastic-mechanical half-sarcomere model that separates the energetic roles of ATP and ADP/Pi in the cross-bridge cycle's free energy landscape. Our results clearly demonstrate that there is a nontrivial dependence of the cross-bridge cycle's kinetics on the independent concentrations of ATP, ADP, and Pi. The simplicity of the proposed model allows for analytical solutions of the more basic systems, which provide novel insight into the dominant mechanisms driving some of the experimentally observed contractile phenomena.

Co-Pyrolysis of Mushroom Residue Blended with Pine Sawdust/Wheat Straw for Sustainable Utilization of Biomass Wastes: Thermal Characteristics, Kinetic/Thermodynamic Analysis, and Structure Evolution of Co-Pyrolytic Char

Co-pyrolysis technology is considered to be one of the most promising methods for the sustainable utilization of biomass wastes, as it can realize waste reduction and convert wastes into high-value-added products with little impact on the environment. The evaluation of thermal characteristics and product properties is necessary for understanding this technique. In this paper, thermal characteristics and kinetic and thermodynamic analysis during the co-pyrolysis of mushroom residue (MR) with pine sawdust (PS) or wheat straw (WS) were investigated in a TGA. The carbon structure and surface textures of co-pyrolytic char were explored using Raman spectroscopy and a scanning electron microscope. As the PS or WS mass ratio increased, the devolatilization index increased obviously, indicating that volatile release was promoted and concentrated. Weak interactions were observed between 250 and 400 °C during the co-pyrolysis process, which primarily affected the mass transfer, resulting in a change in the thermal decomposition temperatures and rates. The interactions had no prominent influence on the volatiles’ yields. The non-additive performance of average activation energies for the blends was observed due to the interactions, and the lowest average activation energy was obtained when the PS or WS mass ratio was 50%. The lower average pre-exponential factor of the blends indicated the reduced complicacy of the pyrolysis reaction. The relatively small deviation between the activation energy and enthalpy change (4.94–5.18 kJ·mol−1) signified the energy sensitivity of product formation. PS promoted the formation of small aromatic rings (<6 fused rings) in co-pyrolytic chars, whereas WS favored the production of larger rings (≥6 fused rings). The surface textures of the co-pyrolytic chars became porous, and the greater fractal dimensions of the surface morphology for the co-pyrolytic chars indicated that the char surface became irregular and rough.

The Ether‐Adduct of a Lewis Superacidic, Dicoordinate Aluminum Hydride Cation and the Ion Affinities of Solvent‐Adducts

AbstractAluminum reagents are widely used as strong Lewis acids for organic transformations and catalysis. In recent years, a variety of Al‐Lewis superacids could be accessed by preparation of aluminum cations paired with weakly‐coordinating anions or by use of perfluorinated substituents at the metal. While the majority of these Al‐Lewis superacids is composed of a tricoordinate Al‐metal atom, examples for dicoordinate Al species are very scarce. In this study, we report the preparation of [(Mes*)Al(H)(OEt2)]+[Al(ORF)4]− (Mes*=2,4,6‐tBu3‐C6H2, RF=C(CF3)3) by reaction of protonated ether [H(OEt2)2]+[Al(ORF)4]− with [Mes*AlH2]2. Structural analysis supported by computed frontier orbitals and atomic charges reveals that the cation is best described as diethylether adduct of dicoordinate [(Mes*)Al(H)]+ and acts as synthon to this low‐coordinate cation. To incorporate the masking of the coordination site by the ether, the enthalpy of dissociation is included in the computed fluoride‐ and hydride ion affinities (XIA) and entropic effects are treated by defining a “free ion affinity” (fXIA), basing on the Gibbs energy change. Hereby, the Lewis acidity of free Lewis acids as well as their solvent adducts can be estimated.

Explanation of Numerical Changes in Energy by New Algebra

New algebra will explain energy change here 1=false 0=true

Influence of selected factors on the energy consumption of frozen logs subjected to thermal treatment in veneer production

ABSTRACT This study puts forward an approach for calculating the specific energy consumption and its components required for heating of frozen logs for veneer production, depending on the logs’ initial temperature and moisture content. The approach is based on the use of two personal models: unsteady model of the temperature distribution along the radius of frozen logs during their thermal treatment and stationary model of the energy consumption of logs subjected to such treatment as a function of its four multifactorial components. The influence of all combinations between five values of the initial temperature of frozen logs from −1 oC to −40 oC and three values of their moisture content from 0.4 kg·kg−1 –0.8 kg·kg−1 on the specific energy required to heat and placticize beech logs with a diameter of 0.4 m at operating temperature of the steaming or boiling medium of 80 oC was investigated. The obtained results show that this energy changes in the range from 46 kWh·m−3 (at −1 oC and 0.4 kg·kg−1) to 114 kWh·m−3 (at −40 oC and 0.8 kg·kg−1) The approach could be applied to calculate the energy and its components required for carrying out of the thermal treatment of various frozen capillary-porous materials.

Inflation comovement in emerging economies: The facts and impact of global prices

The traditional notion that inflation is a domestic monetary phenomenon has been challenged by the existence of global inflationary factors that cause inflation comovement patterns. Understanding and estimating such comovement and its drivers is critical for effective policymaking. This study analyzes the temporal pattern and determining factors of inflation comovement of Commonwealth of Independent States (CIS) countries, comparing it to other former Eastern Bloc economies that entered the European Union (EU), and to other groups of advanced economies. We use monthly data on 26 countries classified into four groups and examine headline, core, food and utilities inflation from December 2006 to October 2021. We find that inflation comovement increased over the study period for all inflation categories, except food inflation, for all groups of countries, with comovement in CIS countries being the lowest. Moreover, positive changes in global energy prices significantly impact CIS inflation comovement, but not negative changes.

Investigating electrocatalytic properties of β12-borophene as a cathode material for an efficient lithium-oxygen battery: a first-principles study

Responding to the pressing need to mitigate climate change effects due to fossil fuel consumption, there is a collective push to transition towards renewable and clean energy sources. However, the effectiveness of this move depends on an efficient energy storage system that surpasses current lithium-ion battery technology. The lithium-oxygen battery, having significantly high theoretical specific capacity compared to other systems, has emerged as a promising solution. However, the issues of poor cathode electrode conductivity and slow kinetics during discharge product formation have limited its practical applications. In this work, the first principles-based density functional theory was used to investigate the electrocatalytic properties of β12-borophene as a cathode electrode material for a high-performance lithium-oxygen battery. The adsorption energy, charge density distributions, Gibbs free energy changes, and diffusion energy barriers of lithium superoxide (LiO2) on β12-borophene were calculated. Our findings revealed several important insights: The adsorption energy was found to be − 3.70 eV, suggesting a strong tendency for the LiO2 to remain anchored to the material during the discharging process. The dynamics in the charge density distributions between LiO2 and the β12-borophene substrate exhibited complex behavior. The analysis of the Gibbs free energy changes of the reactions yielded an overpotential of − 1.87 V, this moderate value suggests spontaneous reactions during the formation of the discharge products. Most interestingly, the density of states and band structure analysis suggested the preservation of metallic properties and improved electrical conductivity of the material after the adsorption of LiO2. Additionally, β12-borophene has a relatively low diffusion energy barrier of 1.08 eV, implying effortless diffusion of the LiO2 and an increase in the rate of discharging process. Ultimately, the predicted electronic properties of β12-borophene, make it a strong candidate as a cathode electrode material for an efficient lithium-oxygen battery.

Infectious disease responses to human climate change adaptations.

Many recent studies have examined the impact of predicted changes in temperature and precipitation patterns on infectious diseases under different greenhouse gas emissions scenarios. But these emissions scenarios symbolize more than altered temperature and precipitation regimes; they also represent differing levels of change in energy, transportation, and food production at a global scale to reduce the effects of climate change. The ways humans respond to climate change, either through adaptation or mitigation, have underappreciated, yet hugely impactful effects on infectious disease transmission, often in complex and sometimes nonintuitive ways. Thus, in addition to investigating the direct effects of climate changes on infectious diseases, it is critical to consider how human preventative measures and adaptations to climate change will alter the environments and hosts that support pathogens. Here, we consider the ways that human responses to climate change will likely impact disease risk in both positive and negative ways. We evaluate the evidence for these impacts based on the available data, and identify research directions needed to address climate change while minimizing externalities associated with infectious disease, especially for vulnerable communities. We identify several different human adaptations to climate change that are likely to affect infectious disease risk independently of the effects of climate change itself. We categorize these changes into adaptation strategies to secure access to water, food, and shelter, and mitigation strategies to decrease greenhouse gas emissions. We recognize that adaptation strategies are more likely to have infectious disease consequences for under-resourced communities, and call attention to the need for socio-ecological studies to connect human behavioral responses to climate change and their impacts on infectious disease. Understanding these effects is crucial as climate change intensifies and the global community builds momentum to slow these changes and reduce their impacts on human health, economic productivity, and political stability.

Anticipating how rain-on-snow events will change through the 21st century: lessons from the 1997 new year’s flood event

AbstractThe California-Nevada 1997 New Year’s flood was an atmospheric river (AR)-driven rain-on-snow (RoS) event and remains the costliest in their history. The joint occurrence of saturated soils, rainfall, and snowmelt generated inundation throughout northern California-Nevada. Although AR RoS events are projected to occur more frequently with climate change, the warming sensitivity of their flood drivers across scales remains understudied. We leverage the regionally refined mesh capabilities of the Energy Exascale Earth System Model (RRM-E3SM) to recreate the 1997 New Year’s flood with horizontal grid spacings of 3.5 km across California, with forecast lead times of up to 4 days, and across six warming levels ranging from pre-industrial conditions to $$+3.5\,^\circ$$ + 3.5 ∘ C. We describe the sensitivity of the flood drivers to warming including AR duration and intensity, precipitation phase, intensity and efficiency, snowpack mass and energy changes, and runoff efficiency. Our findings indicate current levels of climate change negligibly influence the flood drivers. At warming levels $$\ge 1.7\,^\circ$$ ≥ 1.7 ∘ C, AR hazard potential increases, snowpack nonlinearly decreases, antecedent soil moisture decreases (except where the snowline retreats), and runoff decreases (except in the southern Sierra Nevada where antecedent snowpack persists). Storm total precipitation increases, but at rates below warming-induced increases in saturation-specific humidity. Warming intensifies short-duration, high-intensity rainfall, particularly where snowfall-to-rainfall transitions occur. This study highlights the nonlinear tradeoffs in 21st-century RoS flood hazards with warming and provides water management and infrastructure investment adaptation considerations.

Effect of iron minerals on formation of hydroandradite during alkali-thermal process

The hydroandradite (HA) is an efficient and ideal desilication product to deal with the bauxite and red mud based on the alkali-thermal process, while the selection of iron source is crucial for the HA generation. This work investigates the effects of various natural iron minerals on the alkali-thermal formation HA in aluminate solution by comparing with synthetic sodium ferrate. The Gibbs free energy changes of HA formation with different iron oxides were calculated based on the complex silicate theory, and the preferential conversion order for HA formation was obtained thermodynamically. The solubility data of various iron minerals in aluminate solution were determined and correlated by the Apelblat model. The contribution order of iron minerals for HA formation was obtained, and the goethite is the best alternative to replace sodium ferrite by comparing to hematite and magnetite. The phase transformation of HA is above 80% in the presence of goethite, and the alkali content in reaction product is as low as 0.20%. Moreover, the effect mechanism of goethite on HA formation was discussed and established.