Laser-Induced Thermal Treatment of Superficial Human Tumors: An Advanced Heating Strategy and Non-Arrhenius Law for Living Tissues

The most interesting, but insufficiently known results obtained by the author in modeling laser-induced hyperthermia of human tumors are discussed. It is important that the traditional equation for the local bio-heat transfer does not work in superficial layers of the body. It is shown also that the classical Arrhenius law is not applicable to living tissues because of the tissue regeneration due to oxygen supplied by the arterial blood. The latter is one of the main reasons of the suggested strategy of laser heating of tumors in the therapeutic window of semitransparency when the tumor asphyxiation is considered as one of important weapons against the cancer. The other advantages of this advanced strategy of a soft thermal treatment (in few of sessions), which is painless for patients, are discussed as well. Some features of modeling various heat transfer modes are also considered. The best choice between the simplest differential models for the radiative transfer calculations is dependent of the particular problem statement. The known finite-difference or finite element algorithms can be preferable in solving transient heat transfer problems. As a rule, it depends on the shape of the computational region. It is expected that this paper will help the colleagues to overcome some typical weaknesses of computational modeling of infrared photothermal treatment of superficial tumors.

Internal Dynamics of Ionic Liquids over a Broad Temperature Range—The Role of the Cation Structure

1H and 19F spin-lattice relaxation experiments have been performed for a series of ionic liquids sharing the same anion: bis(trifluoromethanesulfonyl)imide but including cations of different alkyl chain lengths: butyltriethylammonium, triethyloctylammonium, dodecyltriethylammo-nium and hexadecyltriethylammonium. The studies have been carried out in the temperature range from 383 to 108 K at the resonance frequency of 200 MHz (for 1H). A quantitative analysis of the relaxation data has revealed two dynamical processes for both kinds of ions. The dynamics have been successfully modeled in terms of the Arrhenius law. The timescales of the dynamical processes and their temperature evolution have been discussed in detail, depending on the structure of the cation.

Dielectric Response of KTaO3 Single Crystals Weakly Co-Doped with Li and Mn

Alkali tantalates are encouraging functional materials with versatile properties that make them potential players in microelectronics, photocatalytic processes or medicine. Here, KTaO3 single crystals with 0.27% Li and 0.15% or 0.31% Mn contents determined by inductively coupled plasma spectroscopy analysis are studied at low temperatures using dielectric spectroscopy in a frequency range of 102–106 Hz. Both Li and Mn doping are found to induce separate low-frequency dielectric relaxations of comparable strength in KTaO3. The relaxation dynamics follow the Arrhenius law with activation energy values of ~77 and 107 meV, attributing the relaxation origin to the dipoles formed by off-centre Li+K and Mn2+K ions, respectively.

Rheological Behavior Models of Polymers

We studied and investigated the various viscosimetric and rheological polymers' behaviors during this comprehensive review. The viscosities relate to the investigation of the flux, the deformation, and the polymers' elasticity; we have employed the viscosity since this plays a primordial role in the phenomena flux and implementation of the polymer. The rheology behaviors were investigated for the determination of the physical properties of polymers. The rheological properties are mostly employed for improving polymers implementation. Further, three rheological behaviors models such as Newtonian, pseudo-plastic (Power Law, Law of Tile and Cross Law) and heat-dependent pseudo-plastic (Williams-Landel-Ferry Law (WLF), Law of Tile-Yasuda and Arrhenius law) were studied.

Multistability and rare spontaneous transitions in barotropic β-plane turbulence

We demonstrate that turbulent zonal jets, analogous to Jovian ones, which are quasi-stationary, are actually metastable. After extremely long times, they randomly switch to new configurations with a different number of jets. The genericity of this phenomenon suggests that most quasi-stationary turbulent planetary atmospheres might have many climates and attractors for fixed values of the external forcing parameters. A key message is that this situation will usually not be detected by simply running the numerical models, because of the extremely long mean transition time to change from one climate to another. In order to study such phenomena, we need to use specific tools: rare event algorithms and large deviation theory. With these tools, we make a full statistical mechanics study of a classical barotropic beta-plane quasigeostrophic model. It exhibits robust bimodality with abrupt transitions. We show that new jets spontaneously nucleate from westward jets. The numerically computed mean transition time is consistent with an Arrhenius law showing an exponential decrease of the probability as the Ekman dissipation decreases. This phenomenology is controlled by rare noise-driven paths called instantons. Moreover, we compute the saddles of the corresponding effective dynamics. For the dynamics of states with three alternating jets, we uncover an unexpectedly rich dynamics governed by the symmetric group of permutations, with two distinct families of instantons, which is a surprise for a system where everything seemed stationary in the hundreds of previous simulations of this model. We discuss the future generalization of our approach to more realistic models.

Float Current Analysis for Fast Calendar Aging Assessment of 18650 Li(NiCoAl)O2/Graphite Cells

Float currents are steady-state self-discharge currents after a transient phase—caused by anode overhang, polarization, etc.—is accomplished. The float current is measured in this study with a standard test bench for five 18650 cells (Samsung 25R) at potentiostatic conditions while the temperature is changed in 5 K steps from 5 °C to 60 °C. The entire test is performed in about 100 days resulting in 12 measurement points per cell potential for an Arrhenius representation. The float current follows the Arrhenius law with an activation energy of about 60 kJ/mol. The capacity loss measured at reference condition shows a high correlation to the results of float currents analysis. In contrast to classical calendar aging tests, the performed float current analysis enables determining the aging rate with high precision down to at least 10 °C. Returning from higher temperatures to 30 °C reference temperature shows reducing float currents at 30 °C for increasing temperature steps that may originate from an hysteresis effect that has to be investigated in future publications.

NGHIÊN CỨU SỰ KHUẾCH TÁN CỦA NGUYÊN TỬ XEN KẼ TRONG HỢP KIM XEN KẼ AuSi VỚI CẤU TRÚC LẬP PHƯƠNG TÂM DIỆN

The paper derives analytic expressions of the diffusion coefficient depending on strain and pressure for the interstitial alloy AB with FCC structure by the statistical moment method based on previous studies for metals and semiconductors. Theoretical results are applied to alloy AuSi. Our numerical results satisfy the Arrhenius law

Determination of key-thermodynamic parameters using a kinetic modeling approach to describe the post-consumer poly(ethylene terephthalate) hydrolysis catalyzed by cutinase from Humicola insolens

The search for a straightforward technology for post-consumer poly(ethylene terephthalate) (PC-PET) degradation is essential to develop a circular economy. In this context, PET hydrolases such as cutinases can be used as bioplatforms for this purpose. Humicola insolens cutinase (HiC) is a promising biocatalyst for PC-PET hydrolysis. Therefore, this work evaluated a kinetic model, and it was observed that the HiC seems not to be inhibited by any of the main PET hydrolysis products such as terephthalic acid (TPA), mono-(2-hydroxyethyl) terephthalate (MHET), and bis-(2-hydroxyethyl) terephthalate (BHET). The excellent fitting of the experimental data to a kinetic model based on enzyme-limiting conditions validates its employment for describing the enzymatic PC-PET hydrolysis using two-particle size ranges (0.075-0.250, and 0.250-0.600 mm) and temperatures (40, 50, 55, 60, 70, and 80 ºC). The Arrhenius law provided a reliable parameter (activation energy of 98.9 ± 2.6 kJ mol −1 ) for enzymatic hydrolysis, which compares well with reported values for chemical PET hydrolysis. The thermodynamic parameters of PC-PET hydrolysis corresponded to activation enthalpy of 96.1 ± 3.6 kJ mol -1 and activation entropy of 10.8 ± 9.8 J mol -1 K -1 . Thus, the observed rate enhancement with temperature was attributed to the enthalpic contribution, and this understanding is helpful to the comprehension of enzymatic behavior on hydrolysis reaction.

Lithium tracer diffusion in LiNi0.33Mn0.33Co0.33O2 cathode material for lithium-ion batteries

Lithium tracer diffusivities in LiNi0.33Mn0.33Co0.33O2 cathode material for lithium-ion batteries follows the Arrhenius law with an activation energy of 0.85 eV.

Specific surface area, crystallite size and thermokinetic of oxide formation γ → α-Al2O3 nano powders at 570 – 1470 K

Powders where the γ≈α-Al2O3-nano phases are the priority precursors for catalysts for heterogeneous catalysis with the maximum content of surface 5-coordinated Al centers for Pt attachment. Hydrogenated nano powders (~8 nm) of γ-, γ '-, θ-, κ-Al2O3 soluble in hydrochloric acid were obtained from the processing of aluminum boride powders with an icosahedral structure. Samples, which underwent a step-by-step and single heating of 50-100K heat treatment for 2 hours at temperatures of 570-1470K, were received in quantity of 34. The specific surface area of SВET, m2g-1 was measured by the thermal nitrogen desorption express method of gas chromatography through the GC-1 device. X-ray (phase and coherent), fluorescence and phase chemical-analytical evaluation of the samples were performed. The thermokinetic characteristics of the processes are calculated using the exponential Arrhenius law. Dimensional characteristics of crystallites (10.4-48 nm); specific surface area of powders (213-8.6 m2g-1, SВET); thermokinetic parameters of α-Al2O3 crystallite growth process (V α-Al2O3 - 1.44 10-3 - 6.67 10-3 nm s-1; E α-Al2O3 = 38.7±2.1kJ mol-1; A0 = 0.16±0.0 s-1 along the temperature line 1220-1470K were determined and calculated. The process of dehydration of two OH-groups occurs in the region 570-720K Ea H2O ↑ = 30.5 ± 0.5 kJ mol-1 A0 = 1.33±0.3 s-1. The last group of OH at temperatures of 820 -1070К and a rate of 2.13 10-4 - 4.93 10-4 mol s-1 Ea H2O ↑ = 13.2 ± 0.8 kJ mol-1 A0 = 16.9 ± 0.9 s-1. The activation energy of the phase transition is Ea., γ → α-Al2O3 = 23.9 ± 1.0 kJ mol-1 A0 = 2.01 ± 0.72 s-1 (770-970K) and Ea., γ → α-Al2O3 = 83.5 ± 0.8 kJ mol-1 A0 =(2,05±0,95) 103 s-1 (1070-1170K). It agrees well with the known heat of conversion Eа, γ→α-Al2O3 = 85 kJ mol-1. The TK of γ≈α-Al2O3-nano phases is at 1170K.