Trends In Temperature Dependence Research Articles

Non-Isothermal Thermogravimetric Analysis of Carbonation Reaction for Enhanced CO2 Capture

An in-depth investigation into CaO-based carbonation reaction kinetics for CO2 sorption is being conducted using simultaneous thermal analysis (STA), with the application of advanced thermogravimetric and differential scanning calorimetry techniques. Utilizing advanced thermal analysis system for real-time monitoring of simultaneous measurements of mass changes and thermal effects are conducted, ensuring precision and versatility in data acquisition. The study explores the intricacies of the non-isothermal carbonation process across a wide range of temperatures, shedding light on the temperature-dependent trends in reaction rates. Innovative statistical methods, combining regression techniques and Arrhenius equation, are employed to determine energy and reaction kinetics. The sensitivity of carbonation process to varying pressure conditions is meticulously examined in the study, providing pivotal discernment for optimization of reaction parameters across diverse applications. The integration of STA with statistical modeling alongside systematic analysis of temperature-dependent trends and pressure-order relationships not only enhances the understanding of CO2 capture efficiency but also improves the robustness and accuracy of the findings. Furthermore, meticulous cross-validation with existing studies provides a critical evaluation of the experimental approach’s precision and limitations. This study enhances understanding of CaO carbonation kinetics, providing practical implications for carbon capture processes and contributing to sustainable industrial processes.

Low Vapor Pressure Solvents for Single-Molecule Junction Measurements.

Nonpolar solvents commonly used in scanning tunneling microscope-based break junction measurements exhibit hazards and relatively low boiling points (bp) that limit the scope of solution experiments at elevated temperatures. Here we show that low toxicity, ultrahigh bp solvents such as bis(2-ethylhexyl) adipate (bp = 417 °C) and squalane (457 °C) can be used to probe molecular junctions at ≥100 °C. With these, we extend solvent- and temperature-dependent conductance trends for junction components such as 4,4'-bipyridine and thiomethyl-terminated oligophenylenes and reveal the gold snapback distance is larger at 100 °C due to increased surface atom mobility. We further show the rate of surface transmetalation and homocoupling reactions using phenylboronic acids increases at 100 °C, while junctions comprising anticipated boroxine condensation products form only at room temperature in an anhydrous glovebox atmosphere. Overall, this work demonstrates the utility of low vapor pressure solvents for the comprehensive characterization of junction properties and chemical reactivity at the single-molecule limit.

Temperature and pressure dependencies of Sm valence in SmB[formula omitted] Kondo insulator probed by x-ray absorption spectroscopy

Pressure and temperature induced valence changes in the Kondo insulator SmB6 have been investigated using x-ray absorption spectroscopy (XAS) along several isobaric cooling runs and one isothermal compression. The average valence of Sm at various pressure and temperature conditions is extracted from high quality XAS data by peak fitting procedures. The temperature dependence of the Sm valence at ambient pressure shows changes of slope near the known characteristic temperatures of gap formation (120 K) and the in-gap state (50 K). At higher pressures the average valence also shows similar temperature dependent trends upon cooling but the slope changes are less pronounced. This behavior is discussed in relation to the possible existence of an underlying first order valence transition and its critical end point. At constant temperature (T=20 K), the Sm valence increases rapidly with pressure; however, it remains far below the expected integer value (3+) near the onset of the magnetic ordering and gap closure. In addition, the local structure of SmB6 at ambient conditions has been analyzed using extended x-ray absorption fine structure.

Thermodynamic properties of TPAC-EG deep eutectic solvents: A study based on the IGC method with molecular simulations

The study of thermodynamic properties and intermolecular interactions in deep eutectic solvents (DES) is an important innovative step in the development of DES. This research focuses on the synthesis of DES using a 1:2 M ratio of tetrapropylammonium chloride and ethylene glycol. Inverse gas chromatography (IGC) techniques are used to investigate DES of thermodynamics in the temperature range of 303.15–333.15 K. Additionally, molecular dynamics (MD) simulations and density functional theory (DFT) are used to explore intermolecular interactions in DES at both molecular and atomic levels. The research findings yield crucial insights, including the successful determination of infinite dilution activity coefficients, Flory-Huggin’s interaction parameters, solubility parameters, and Abraham solvation parameters of DES through IGC techniques. A careful study of the temperature-dependent trends in these parameters is provided. Analyses of structural properties, including radial distribution functions, hydrogen bond counts, and thermal fluctuation indices, reveal that, at experiments temperatures, the amount and nature of intermolecular hydrogen bonds in binary mixtures are the main factors influencing the thermodynamic properties of DES. Finally, based on DFT calculations, a quantitative assessment of the molecular interaction mechanisms of DES at the atomic level confirms the predominant role of hydrogen bonding in DES formation, with multicenter hydrogen bonds characterized by stronger hydrogen bond strengths emerging as the primary type.

Effects of Water Content on the Transport and Thermodynamic Properties of Phosphonium Ionic Liquids.

We present a numerical investigation of the influence of water content on the dynamic properties of a family of phosphonium-based room-temperature ionic liquids. The study presents a compelling correlation between structural changes in water-ionic liquid solutions and thermodynamic and transport properties across diverse systems. The results for phosphonium ionic liquids are compared with 1-butyl-3-methylimidazolium hexaphosphate ([bmim]PF6) as a reference. Through this approach, phosphonium cation structure-related characteristics can be identified and placed within the broader context of ionic liquids. These insights are underpinned by observed changes in interaction energy, boiling point, diffusion rate, and viscosity, highlighting the crucial role of water molecules in weakening the strength of interactions between ions within the ionic liquid. The investigation also explains temperature-dependent trends in phosphonium cations, showing that alkyl group length and molecular symmetry are important tuning parameters for the strength of Coulomb interactions. These results contribute to a refined understanding of phosphonium ionic liquid behavior in the presence of water, offering valuable insights for optimizing their use in diverse fields.

Optimizing hydrothermal treatment for sustainable valorization and fatty acid recovery from food waste

This study employs response surface methodology and a central composite design (CCD) to optimize hydrothermal treatment (HTT) conditions for the valorization of food waste (FW). Lab-scale pressure reactor-based HTT processes are investigated to detect the effects of temperature (220–340 °C) and resident time (90–260 min) on elemental composition and fatty acid recovery in the hydrothermal liquid. Central to the study is the identification of temperature as the primary factor influencing food waste conversion during the HTT process, showcasing its impact on HTT product yields. The liquid fraction, rich in saturated fatty acids (SFA), demonstrates a temperature-dependent trend, with higher temperatures favoring SFA recovery. Specifically, HTT at 340 °C in 180 min exhibits the highest SFA percentages, reaching up to 52.5 wt%. The study establishes HTT as a promising avenue for nutrient recovery, with the liquid fraction yielding approximately 95% at optimized conditions. Furthermore, statistical analysis using response surface methodology predicts the optimal achievable yields for hydrochar and hydrothermal liquid at 6.15% and 93.85%, respectively, obtained at 320 °C for 200 min.

Probing pharmaceutically important amino acids L-isoleucine and L-tyrosine Solubilities: Unraveling the solvation thermodynamics in diverse mixed solvent systems

The study specifically investigates the solubilities of L-isoleucine and L-tyrosine in water-mixed solvent systems (DMF, DMSO, and ACN), exploring the behaviour of amino acids in complex environments. The experimental methods prioritize meticulous solvent purification to ensure reliable results. The work explores solubility data, uncovering temperature-dependent trends and intricate interactions influencing solubility in the chosen mixed solvent systems. The study emphasizes the impact of thermodynamic properties, solvent-solvent interactions, and amino acid structure on solubility patterns. The broader implications highlight the relevance of understanding amino acid behaviour in diverse solvent environments, offering potential applications in cosmetics and pharmaceutical industries. The distinct solubility patterns contribute valuable insights, enhancing on the understanding of the solution stability and interactions of L-isoleucine and L-tyrosine in different solvent systems. In conclusion, work suggests the enhanced utilization of L-isoleucine and L-tyrosine in various industries, driven by a profound understanding of their solubility in mixed solvent systems. The research expands our knowledge of amino acid behaviour, paving the way for advancements in industries relying on protein-based products and technologies.

Planckian behavior of cuprates at the pseudogap critical point simulated via flat electron-boson spectral density

Planckian behavior has been recently observed in La1·76Sr0·24CuO4 at the pseudogap critical point. The Planckian behavior takes place in an intriguing quantum metallic state at a quantum critical point. Here, the Planckian behavior was simulated with an energy-independent (or flat) and weakly temperature-dependent electron-boson spectral density (EBSD) function by using a generalized Allen's (Shulga's) formula. We obtained various optical quantities from the flat EBSD function, such as the optical scattering rate, the optical effective mass, and the optical conductivity. These quantities are well fitted with the recently observed Planckian behavior. Fermi-liquid behavior was also simulated with an energy-linear and temperature-independent EBSD function. The EBSD functions agree well with the overall doping- and temperature-dependent trends of the EBSD function obtained from the optically measured spectra of cuprate systems, which can be crucial for understanding the microscopic electron-pairing mechanism for high-Tc superconductivity in cuprates.

Proton pathways via free volumes: A positron annihilation lifetime spectroscopy (PALS) investigation of proton conductivity in SPEEK-PEG-TMOS composites

This study investigates the ionic conductivity and dielectric properties of SPEEK-PEG-TMOS solid-state polymer electrolytes across a broad frequency spectrum (0.1–1000 kHz). Proton transport mechanisms were explored over an extensive temperature range, and positron annihilation lifetime spectroscopy (PALS) was employed to elucidate the roles of free volumes in the transport mechanism. At elevated temperatures, sulfonic acid groups and free volume defects predominantly govern the conductivity in all polymer electrolytes. PEG incorporation significantly improved proton conductivity at low temperatures, while the presence of TMOS and higher PEG content have elevated conductivity at higher temperatures. Proton conductivity mechanisms at elevated temperatures are influenced by SPEEK's intrinsic proton conductivity, PEG's plasticizing effect, acid-base interactions, and the presence of free volumes. PALS analysis reveals temperature-dependent trends in the o-Ps lifetime, intensity, and free volume fraction, increasing linearly with temperature due to thermal expansion. PEG content modulated this trend, with lower PEG content samples displaying lower thermal expansion slopes, and higher PEG content samples exhibiting more substantial increases in hole-free volume. The o-Ps intensity displayed a temperature-dependent change attributed to PEG's thermal expansion limitations. These insights contributed to a comprehensive understanding of the intricate interplay between PEG content, thermal expansion, and free volume in SPEEK-PEG-TMOS composites. The study has implications for material science applications, particularly in the development of high-temperature, anhydrous proton-conductive systems.

Unveiling the Potential of Corn Cob Biochar: Analysis of Microstructure and Composition with Emphasis on Interaction with NO2.

In the context of sustainable solutions, this study examines the pyrolysis process applied to corn cobs, with the aim of producing biochar and assessing its effectiveness in combating air pollution. In particular, it examines the influence of different pyrolysis temperatures on biochar properties. The results reveal a temperature-dependent trend in biochar yield, which peaks at 400 °C, accompanied by changes in elemental composition indicating increased stability and extended shelf life. In addition, high pyrolysis temperatures, above 400 °C, produce biochars with enlarged surfaces and improved pore structures. Notably, the highest pyrolysis temperature explored in this study is 600 °C, which significantly influences the observed properties of biochars. This study also explores the potential of biochar as an NO2 adsorbent, as identified by chemical interactions revealed by X-ray photoelectron spectroscopy (XPS) analysis. This research presents a promising and sustainable approach to tackling air pollution using corn cob biochar, providing insight into optimized production methods and its potential application as an effective NO2 adsorbent to improve air quality.

Enhanced C2-CN sub-mechanism: Impact on NO/N2O and soot precursor yields during C2H2/HCN oxidation

The combustion of hydrocarbon-ammonia fuels poses challenges related to the formation of soot and nitrogen oxides (NOx) emissions. Various kinetic mechanisms have been developed to describe the pathways of soot and NOx formation, but limited attention has been paid to the role of the C2-CN species, such as HC3N and CH2CHCN, in influencing the yields of soot and NOx. To address this gap, we present a detailed C2-CN sub-mechanism integrated into a NOx and polycyclic aromatic hydrocarbons (PAHs) kinetic model. The rate constants of the barrierless association reactions of C2H+CN, C2H3+CN, C2H5+CN, and CH3+CH2CN were updated using the variable reaction coordinate transition state theory (VRC-TST). We numerically investigated the oxidation of C2H2 and HCN at equivalence ratios of 2.0 and 3.0, which are major precursors for NOx and PAHs, in a perfectly stirred reactor (PSR) employing two kinetic models (with/without the developed C2-CN sub-mechanism). By comparing the rates of production (ROPs) obtained via both models, we analyzed the formation pathways of NO/N2O and Benzo(ghi)fluoranthene (BGHIF). Our findings reveal temperature-dependent trends in the calculated rate constants of C2H5+CN and CH3+CH2CN associations (positive dependence) as well as C2H+CN and C2H3+CN associations (negative dependence). The peak mole fractions of BGHIF at equivalence ratio (φ) of 2.0 and 3.0 predicted by the updated mechanism were 18.4 % and 13.6 % lower than the base mechanism. This reduction can be attributed to an additional consumption channel of C2H2 (C2H2+CN=HC3N+H) predicted by the C2-CN sub-mechanism. Furthermore, the C2-CN sub-mechanism exhibited a stronger suppression effect on N2O formation compared with NO formation at φ=2.0 and 3.0. This limitation can be explained by an additional consumption channel of CN via CN+C2H2=HC3N+H, resulting in decreased NO/N2O through the reaction sequence CN→NO→N2O and CN→NCO→HNCO→NH2→HNO→NO→N2O.

First-principles study of electronic, optical, magnetic, and thermoelectric properties of novel Sr2UXO6 (X = Mn, Zn) double perovskites

Based on Density Functional Theory, the first-principles investigation is carried out to calculate the optoelectronic, magnetic, and thermoelectric transport properties of novel Sr2UXO6 (X = Mn, Zn) double perovskites in their monoclinic structural phase. The electronic band structures and DOS analysis investigations suggest that these materials have a semiconducting nature. To investigate the magnetic behavior spin-polarized calculations have been carried out. The magnetic studies predict the antiferromagnetic (AFM) nature of Sr2UMnO6 and the non-magnetic (NM) nature of Sr2UZnO6. The electrical conductivity analysis demonstrated semiconducting behavior for both materials, with both materials exhibiting n-type conductivity. The Seebeck coefficient indicated the shift in carrier behavior, while thermal conductivity revealed distinct temperature-dependent trends. These results contribute to understanding and optimizing the thermoelectric performance of these materials for energy conversion applications. The optical parameters including both the real and the imaginary part of the complex dielectric function, absorption coefficient, refractive index, energy loss, and reflectivity in the energy 0–14 eV have been calculated and discussed. The optical results show that the materials demonstrate great potential for applications in optoelectronics due to their notable energy absorption characteristics.

Distinct Temperature Trends in the Uptake of Gaseous n-Butylamine on Two Solid Diacids.

Uptake coefficients of n-butylamine (BA) on solid succinic (SA) and glutaric acids (GA) from 298 to 177 K were measured using a newly combined Knudsen cell temperature-programmed desorption apparatus. The uptake coefficients on SA increase monotonically from (1.9 ± 0.5) × 10-4 at 298 K to 0.14 ± 0.05 at 177 K (errors represent 2σ statistical errors, overall errors are estimated to be ±60%). This is consistent with a surface reaction mechanism to form solid aminium carboxylate. In contrast, the uptake coefficients on GA increase from 0.11 ± 0.04 at 298 K to 0.25 ± 0.04 at 248 K but then decrease to 0.030 ± 0.010 at 177 K. This unusual trend in temperature dependence of the uptake coefficient is due to formation of an ionic liquid (IL) layer upon the surface reaction of BA with GA, leading to a competition between the rate of desorption of BA and the rates of diffusion and reaction within the IL. Overall, the kinetic multi-layer model of aerosol surface and bulk chemistry (KM-SUB) satisfactorily reproduces these unique trends. This work provides mechanistic insight and predictive capability for the temperature-dependence of reactive uptake processes involving multiple phase changes upon surface reaction.

Thermoelectric properties of Fe2VAl in the temperature range 300–800 K: A combined experimental and theoretical study

Here, the experimentally observed thermoelectric (TE) properties of Fe2VAl are understood through electronic structure calculations in the temperature range of 300–800 K. The Seebeck coefficient (S) is observed as ∼−138μV/K at 300 K. Then, the |S| decreases with increase in temperature, with a value of ∼−18μV/K at 800 K. The temperature dependence of electrical conductivity, σ (thermal conductivity, κ) exhibits the increasing (decreasing) trend with values of ∼1.2× 105Ω−1 m−1 (∼23.7 W/m K) and ∼2.2× 105Ω−1 m−1 (∼15.3 W/m K) at 300 K and 800 K, respectively. In order to understand these transport properties, the DFT based semi-classical Boltzmann theory is used. The contributions of multi-band electron and hole pockets are found to be mainly responsible for the temperature dependent trend of these properties. The present study suggests that DFT based calculations provide reasonably good explanations of experimental TE properties of Fe2VAl in the high-temperature range of 300–800 K.

Importance of temperature dependence of interface traps in high-k metal gate stacks for silicon spin-qubit development

While semiconductor-based spin qubits have demonstrated promising fidelities exceeding 99.9%, their coherence time is limited by the presence of charge noise. However, fast process optimization for reduced charge noise becomes challenging due to the time-consuming nature of cryogenic measurements. Hence, this work explores low frequency analysis methods to determine interface trap densities, their temperature dependence, and correlation with observed noise levels. The herein presented results provide evidence for strong temperature dependence of the interface trap density. Moreover, good agreement is observed between charge pumping and conductance-based methods. Finally, differences in temperature dependent trends of flicker noise are observed, indicating additional influences, which need to be considered for further device optimization.

The roles of carbonate, borate, and bicarbonate ions in affecting zooplankton hatching success under ocean acidification

Two ocean acidification studies about egg hatching success (HS) in geographically important marine copepods, Calanus finmarchicus and C. helgolandicus, were reanalyzed with improved statistical procedures. The new results at low and moderate levels of seawater acidification showed no HS inhibition at normal habitat temperatures but statistically significant inhibition at warmer and colder temperatures. These HS results were compared with seawater carbonate system and borate concentrations from precise seawater measurements. The temperature dependent differences in HS could not be directly explained by changes in the seawater concentrations of either H+, bicarbonate (HCO3−), or CO2* (CO2* being the sum of unhydrated CO2 and H2CO3). In contrast, HS differences did match trends in seawater carbonate (CO32−) concentrations. A numerical model was developed which evaluates the concentrations of O2 or CO2*, HCO3−, and CO32− at the cellular level across an egg and embryo by considering both gas diffusion with the seawater and respiration by the embryo. Again, temperature-dependent trends in HS could not be explained changes in intracellular CO2* or HCO3− concentrations, but HS did trend with the changes in intracellular CO32− concentrations. Carbonate ions form strong coordination complexes with metals, so acidification-driven decreases in external seawater carbonate concentrations, which are amplified at warmer temperatures, could release injurious metals, thus driving the HS inhibition at warmer temperatures. Increases in cytoplasmic carbonate concentrations at warmer temperatures caused by seawater acidification could complex with biochemically-needed nutrient-type metals within the cells, also causing the increased HS inhibition at warmer temperatures. Furthermore, boron is essential in chemically signaling within and between cells. Seawater borate concentrations were closely correlated with HS inhibition via Michaelis-Menton equations, suggesting that acidification-driven decreases in seawater borate concentrations may also inhibit HS. Finally, the acidification-driven increases in CO2 diffusion into cells dramatically increased intracellular bicarbonate concentrations. At mild levels of seawater acidification, an organism might compensate by exporting bicarbonate from the cells to the haemolymph and then to the seawater. Although the energetic cost, as percentage of ATP production, might be high, increased respiration rates at warmer temperatures might better allow the organism to survive. However, as temperature is lowered, the cellular respiration rate declines more rapidly with respect to temperature than does the gas diffusion coefficient. Consequently, bicarbonate accumulation driven by inward CO2 diffusion might overwhelm the egg's bicarbonate export capacity at colder temperatures, explaining the colder temperature HS inhibition.

Fast Motions Dominate Dynamics of Intrinsically Disordered Tau Protein at High Temperatures.

Reorientational dynamics of intrinsically disordered proteins (IDPs) contain multiple motions often clustered around three motional modes: ultrafast librational motions of amide groups, fast local backbone conformational fluctuations and slow chain segmental motions. This dynamic picture is mainly based on 15 N NMR relaxation studies of IDPs at relatively low temperatures where the amide-water proton exchange rates are sufficiently small. Less is known, however, about the dynamics of IDPs at more physiological temperatures. Here, we investigate protein dynamics in a 441-residue long IDP, tau protein, in the temperature range from 0-25 °C, using 15 N NMR relaxation rates and spectral density analysis. While at these temperatures relaxation rates are still better described in terms of amide group librational motions, local backbone dynamics and chain segmental motions, the temperature-dependent trend of spectral densities suggests that the timescales of fast backbone conformational fluctuations and slower chain segmental motions might become inseparable at higher temperatures. Our data demonstrate the remarkable dynamic plasticity of this prototypical IDP and highlight the need for dynamic studies of IDPs at multiple temperatures.

Slow methyl axes motions in perdeuterated villin headpiece subdomain probed by cross-correlated NMR relaxation measurements.

Protein methyl groups can participate in multiple motional modes on different time scales. Sub-nanosecond to nano-second time scale motions of methyl axes are particularly challenging to detect for small proteins in solutions. In this work we employ NMR relaxation interference between the methyl H-H/H-C dipole-dipole interactions [Sun&Tugarinov, J. Magn. Reason. 2012] to characterize methyl axes motions as a function of temperature in a small model protein villin headpiece subdomain (HP36), in which all non-exchangeable protons are deuterated with the exception of methyl groups of leucine and valine residues. The data points to the existence of slow motional modes of methyl axes on sub-nanosecond to nanosecond time scales. Further, at high temperatures for which the overall tumbling of the protein is on the order of 2 ns, we observe a coupling between the slow internal motion and the overall molecular tumbling, based on the anomalous order parameters and their temperature-dependent trends. The addition of 28%(w/w) glycerol-d8 increases the viscosity of the solvent and separates the timescales of internal and overall tumbling, thus permitting for another view of the necessity of the coupling assumption for these sites at high temperatures.

Ablation threshold and temperature dependent thermal conductivity of high entropy carbide thin films

High entropy carbides (HECs) are a promising new class of ultra-high temperature ceramics that could provide novel material solutions for leading edges of hypersonic vehicles, which can reach temperatures > 3,500 �C and experience extreme thermal gradients. Although the mechanical and thermal properties of HECs have been studied extensively at room temperature, few works have examined HEC properties at high temperatures or considered these materials� responses to thermal shock. In this work, we measure the thermal conductivity of a five-cation HEC up to 1200 �C. We find that thermal conductivity increases with temperature, consistent with trends demonstrated in single-metal carbides. We also measure thermal conductivity of an HEC deposited with varying CH4 flow rate, and find that although thermal conductivity is reduced when carbon content surpasses stoichiometric concentrations, the films all exhibited the same temperature dependent trends regardless of carbon content. To compare the thermal shock resistance of HECs with a refractory carbide, we conduct pulsed laser ablation measurements to determine the fluence threshold the HECs can withstand before damaging. We find that this metric for the average bond strength trends with the theoretical hardness of the HECs as expected.

Hydrogen effects on thermal diffusivity and electrical resistivity of zircaloy cladding

Thermal diffusivity measurements on Zirconium-based cladding materials have historically been a challenge due to the difficulty to measure on specimens with curved geometries, including nuclear grade Zircaloy cladding materials. In this work, we first used laser flash analysis method and four-probe configuration method to measure the thermal diffusivity and electrical resistivity of Zircaloy tubes respectively, which show good agreement with Zircaloy plates in this work, as well as previously published data. The consistent results proved the applicability of the laser flash analysis setup and four-probe configuration method for investigating thermal diffusivity and electrical resistivity of Zircaloy tubes. We further investigated the hydrogen effect on thermal diffusivity and electrical resistivity of Zircaloy. Hydrogen plays significant roles in the thermal diffusivity of Zircaloy, which depends on the hydrogen concentration. For higher hydrogen contents (1130 and 1820 wppm in this work), where phase transformation (α-Zr + δ-hydride → α-Zr + β-Zr) occurs at 567 °C, thermal diffusivity decreases as a function of temperature at the α-Zr + δ-hydride phase regime, while increase at higher temperature at the α-Zr + β-Zr phase regime. For low hydrogen concentration, where hydride dissolved into α-Zr matrix phase at higher temperature, the thermal diffusivity is lower than non-hydrided Zircaloy-4 with similar temperature-dependent trends. Such observation demonstrates the hydrogen effects on reducing thermal diffusivity of α-Zr phase. Hydrogen increases the electrical resistivity of Zircaloy. Similar to thermal diffusivity results, the phase transformation causes a reversal of temperature-dependent trends in electrical resistivity results in Zircaloy-4 with higher hydrogen contents.