Fictive temperature, cooling rate, and viscosity of glasses

The physical correlation between the fictive temperature dependence of the cooling rate of the melts and the temperature dependence of the equilibrium viscosity has been found by doing differential scanning calorimetric and viscometric measurements on a silicate melt, and by performing finite element simulations of the fiber drawing from that melt. This correlation is governed by a correlation factor Kc (in Pa K) which is constant and universal for silicate glasses. The factor Kc is obtained in the cooling rate range from 10(-2) to 10(6) K/s and is in good agreement with that theoretically predicted. The physical feature of the correlation is discussed in the paper. When the fictive temperature equals the actual temperature, a linear relation exists between the cooling rate and the Maxwell relaxation rate, the slope of which depends on the fragility of the glass melts. The Avramov equation is extended to describe the cooling rate dependence of the fictive temperature. The cooling rate equation contains only one adjusting parameter, i.e., the fragility parameter alpha.     

Experimental and numerical investigation into the corrosion performance of X100 pipeline steel under a different flow rate in CO2-saturated produced water

Journal of Solid State Electrochemistry - The effect of flow velocity on the corrosion behavior of X100 steel in CO2-saturated produced water (CO2-SPW) was studied. Potentiodynamic polarization...     

Experimental investigation of effects of variation in heating rate,temperature and heat flux on fire properties of a non-charring polymer

Journal of Thermal Analysis and Calorimetry - Differential scanning calorimetry (DSC) technique is used to study the solid reactions in the 2024 Al–Cu–Mg and 2014...     

Influence of temperature on the micellization of sodium dodecylsulfate in water from speed of sound measurements

Speed of sound measurements for aqueous solutions of sodium dodecylsulfate (NaDS) have been carried out from 20 to 45°C at intervals of 5°C. The critical micellar concentrations (cmc) were determined and their change with temperature is discussed. A second change in the speed of sound has been found between 15 to 20mM for temperatures above 20°C. Values for G _m ^o , H _m ^o and S _m ^o for the micellization process have been determined and compared with data previously obtained from other experimental properties. These results confirm that the micellization process of NaDS in water is mainly entropically driven.     

Experimental investigation of the Soret effect in acetone/water and dimethylsulfoxide/water mixtures

The thermal diffusion behavior of acetone/water and dimethylsulfoxide(DMSO)/water mixtures has been experimentally investigated by a transient holographic grating technique named thermal diffusion forced Rayleigh scattering (TDFRS). For both systems a sign change of the Soret coefficient S(T) with varying water content has been predicted by simulations [C. Nieto Draghi et al., J. Chem. Phys. 122, 114503 (2005)]. The sign change of S(T) is confirmed by the experiment. Except for equimolar concentrations of acetone/water the agreement between the experimental and simulation data is reasonable.     

Theoretical and experimental investigation of morphology and temperature effects on adsorption of organic vapors in single-walled carbon nanotubes

Hexane adsorption on single-walled carbon nanotube (SWNT) bundles is studied by both simulation and experimentally using a previously developed computer-aided methodology, which employed a smaller physisorbed probe molecule, nitrogen, to explore the porosity of nanotube samples. Configurational-bias grand canonical Monte Carlo simulation of hexane adsorption on localized sites of the bundles is carried out to predict adsorption on their external surface and in their internal sites. These localized isotherms are then combined into a global isotherm for a given sample by using knowledge of its tube-diameter distribution and structural parameters, such as the fraction of open-ended nanotubes and the external surface area of bundles in samples, which have been independently determined from the standard nitrogen adsorption isotherm. The near-perfect replication of experimental isotherms demonstrates the validity of our method for structural characterization of SWNT samples. The effect of temperature on adsorption is also studied and the simulation results are extrapolated to predict the limiting hexane adsorption capacity of the samples. The similarity between the hexane adsorption isotherms and those of other organic molecules demonstrates that the adsorption mechanisms explored here are not specific to hexane, and that the proposed methodology can be potentially applicable to other sorbates with equal success.     

Conformational changes of poly(N-isopropylacrylamide) chains at air/water interface: effects of temperature, compression rate, and packing density

This study concerns the effects of temperature, compression rate, and packing density on conformational properties of polystyrene-block-poly(N-isopropylacryamide) (PS-b-PNIPAM) diblock copolymer monolayers at the air/water interface using the Langmuir balance technique. The dependency of surface pressure changes on temperature and compression rate is strongly influenced by the conformations of PNIPAM chains at the interface, which can be adjusted by varying the packing density. Specifically, when loops or tails are formed at the interface, PNIPAM chains display thermosensitive properties due to hydration/dehydration and obvious dependence on compression rate. When PNIPAM chains take train conformation at the air/water interface, however, the surface pressure changes are nearly independent of temperature and compression rate because almost all segments of the PNIPAM chains are adsorbed at the interface and the nonpolar isopropyl groups are preferentially oriented toward the air. Our work reveals that one could manipulate stimuli-responsive properties of PNIPAM chains at the interface simply by adjusting the conformations of PNIPAM chains.     

The effect of cooling rate on the solidification and microstructure evolution in duplex stainless steel

The effects of the cooling rate on the solidification and microstructure evolution in the duplex stainless steel SAF 2205 was studied using DSC and light microscopy. A ferritoscope was used to measure the ferrite content. It was revealed that the cooling rate has an influence on the ??-ferrite nucleation temperature and the width of the solidification interval. Moreover, with an increase in cooling rate, the content of ??-ferrite increases, while the quantity of austenite in the ferrite matrix decreases and its morphology changes to acicular. A two-cycle DSC experiment made possible a more accurate interpretation of the collected data.     

The effect of temperature, pressure, exposure time, and depressurization rate on lipase activity in SCCO2

We investigated the influence of temperature, pressure, exposure time, and decompression rate on lipase activity in high-pressure CO₂ medium. A high-pressure, variable-volume view cell was employed in the experiments, varying the temperature from 30 to 70°C in the pressure range of 70–250 bar at various high-pressure exposure times (60–360 min) and adopting several decompression rates (10–200 kg/[m³·min]). The results obtained show that an increase in temperature and density led to an enhancement of enzyme activity losses while the decompression rates had a weak influence on enzyme inactivation.     

ANN modelling and experimental investigation on effective thermal conductivity of ethylene glycol:water nanofluids

Journal of Thermal Analysis and Calorimetry - In this study, ethylene glycol (EG)–water (35:65 %v)-based nanofluids have been prepared to study enhancement in thermal conductivity....     

Structural and compositional variations in Ta3N5 produced by high-temperature ammonolysis of tantalum oxide

A series of samples of Ta₃N₅ (Cmcm, , , ) have been produced by high-temperature ammonolysis of amorphous tantalum oxide under various temperature and heating time regimes. These were characterised by powder diffraction (X-ray and neutron), combustion microanalysis, thermogravimetric analysis and transmission electron microscopy. All samples were found to contain oxide in the 3-coordinate anion site and the b-axis length was sensitive to compositional variation. Samples heated for longer times at higher temperatures were anion deficient. The compositions of the samples have been related to their optical band gap UV-visible spectra. This work highlights the importance of careful compositional analysis when samples of nitride materials are produced for real-world applications.     

Low temperature structural variations and molar heat capacity of stolzite, PbWO4

The crystal structure, thermal expansion and heat capacity of PbWO₄ (mineral name stolzite) scintillator material were comprehensively studied over a wide temperature range. No phase transitions were found down to 2 K (I4₁/a, scheelite structure type). A distinct feature of the temperature induced structural variations in PbWO₄ are the different thermal elongations of shorter and longer Pb-O distances. The low-temperature thermal expansion of PbWO₄ was parameterized on the basis of the 1st order Grüneisen approximation using a Debye function for the internal energy with a Debye temperature of 237 K, a bulk modulus of 67 GPa and a Grüneisen parameter of 1.08. The expansion along the c-axis is about 2.5-3 times higher in the range 23-290 K than along the a-direction. This pronounced anisotropy of the thermal expansion arises from the arrangements of rigid tetrahedral WO₄²⁻ units along 〈100〉-directions while Pb²⁺ cations occupy the sites between WO₄²⁻ in 〈001〉-directions.     

Spectroscopic and microscopic investigation of gold nanoparticle formation: ligand and temperature effects on rate and particle size

We report a spectroscopic and microscopic investigation of the synthesis of gold nanoparticles (AuNPs) with average sizes of less than 5 nm. The slow reduction and AuNP formation processes that occur by using 9-borabicyclo[3.3.1]nonane (9-BBN) as a reducing agent enabled a time-dependent investigation based on standard UV-vis spectroscopy and transmission electron microscopy (TEM) analyses. This is in contrast to other borohydride-based syntheses of thiolate monolayer protected AuNPs which form particles very rapidly. We investigated the formation of 1-octadecanethiol (ODT) protected AuNPs with average diameters of 1.5-4.3 nm. By studying the progression of nanoparticle formation over time, we find that the nucleation rate and the growth time, which are interlinked with the amount of ODT and the temperature, influence the size and the size dispersion of the AuNPs. High-resolution TEM (HRTEM) analyses also suggest that the nanoparticles are highly single crystalline throughout the synthesis and appear to be formed by a diffusion-controlled Ostwald-ripening growth mechanism.     

Experimental investigation of the effect of initial fuel particle shape, size and bed temperature on devolatilization of single wood particle in a hot fluidized bed

Considerable amount of investigation on the subject of devolatilization of wood is found in the open literature. However, a systematic study of the effect of initial particle size and shape, and bed temperature on devolatilization time and char yield of wood in a hot fluidized bed is still missing. This paper attempts to fill this gap through a systematic experimental investigation to determine the devolatilization time and char yield of a typical woody biomass, “Casuarina equisetifolia” particles of different initial sizes and shapes at various fluidized bed temperatures. Experiments are conducted using 10, 15, 20, and 25 mm Casuarina wood particles of three shapes, namely, cube, cylinder, and sphere at bed temperatures of 1023, 1123, and 1223 K.It is found that the initial wood particle size has the strongest influence on devolatilization time followed by the shape of initial wood particle and the bed temperature. Correlation for devolatilization time (τ_d) as a function of initial wood particle size (d_eq), sphericity (?), and bed temperature (T_b), is developed using 573 experimental data points exhibiting a correlation coefficient of 0.96 and predictions falling well within a deviation band of ±20%. The predictions of the present correlation are compared with the predictions of the existing correlations in literature for conditions also out of the present study and the deviation is found to be ±30%.Char yield, defined as the ratio of the residual mass at the end of devolatilization process to the initial mass of the wood particle is found to be in the range of 9-14% for all sizes, shapes, and bed temperatures. Char yield does not depict any definite trend with the variation of initial particle size, shape and bed temperature.     

The influence of shear rate, temperature and chain conformation on the critical concentration c

 When viscometry is used, a crossover phenomenon is observed separating the dilute solutions into extremely dilute solutions and dilute solutions. The critical concentration c ^**, determined from this crossover phenomenon, strongly depends on the shear rate in the solution. At very high values of shear rate the critical concentration c ^** becomes very low and depends only on the contour length of the elongated chains of different polymers. An increase of the temperature induces an increase of c ^** because the relaxation time of the chains decreases. If a polymer adopts a rodlike conformation (in a given solvent at a given temperature) the excluded volume of its chains increases and its critical concentration c ^** decreases. Received: 14 October 1996 Accepted: 3 March 1997     

A high-temperature Raman spectroscopic investigation of the potassium tetrasilicate in glassy, supercooled, and liquid states

Raman spectra of K2Si4O9 were measured over a broad temperature range including the glassy, supercooled, and molten states in an effort to follow the structural changes caused by temperature variation. Potassium tetrasilicate glass has been prepared using a containerless method and a CO2 laser for heating and melting the samples and thus avoiding contamination induced by the walls of the crucibles. Systematic Raman intensity measurements caused by temperature variation have been performed in order to elucidate the induced structural changes in the high-frequency stretching and in the three- and four-membered ring breathing vibration regions. The high-frequency symmetric stretching vibrations of the nonbridging Si-O bond are associated to the presence of two distinct types of tetrahedral units with terminal oxygen atoms. The low-frequency Raman spectra reveal the, well resolved, presence of the boson peak at temperatures above the melting point. The temperature dependence of the boson peak energy has also been determined and compared with that of the sound velocities of potassium tetrasilicate. The results are discussed in the context of recent experimental and theoretical works.     

Seasonal and diurnal variations of radon/thoron exhalation rate in Kanto-loam area in Japan

Radon and thoron concentration in the outdoor environment are affected by the magnitude of the exhalation rate that can vary diurnally and seasonally. This paper presents measurement results of radon and thoron exhalation rates and gamma-ray dose rate in different season at same location points in Gunma Prefecture Japan. Exhalation rates were measured by the MSZ instrument which is based on the accumulation method. Three measurement points Katashina Village, Midori City and Takasaki City were selected for measurement. Soil water saturation and soil temperature were measured to investigate their relationship with exhalation rate. The diurnal variation of exhalation rate may be correlated with soil temperature but no clear relationship was found between them. The gamma-ray dose rate do not vary significantly at the same places even in different season. The average radon exhalation rates were 11 ± 2, 2 ± 1, 5 ± 3 and 11 ± 4 mBq m⁻² s⁻¹ for spring, summer, autumn and winter, respectively. Those for thoron were 1,100 ± 100, 120 ± 30, 250 ± 80 and 860 ± 140 mBq m⁻² s⁻¹. Thus there was a variation of radon and thoron exhalation rate with different seasons. The radon and thoron exhalation rates in the summer and autumn surveys are higher than those in the spring and winter surveys which were affected by rainfall. It indicates that water saturation is an influential factor for radon and thoron exhalation rates.     

A reevaluation of low temperature experimental rate data for the reactions of O atoms with methane,ethane, and neopentane

The experimental data for the reactions of oxygen atoms with methane, ethane, and neopentane at temperatures below ca. 600 K have been reexamined. In the case of CH₄ and C₂H₆ reactions, detailed computer models have been assembled to test the assumptions regarding stoichiometries that were made in the original studies in order to derive elementary rate coefficients from the experimentally observed reaction rates. It was found in both cases that the measurements are especially sensitive to secondary reactions not taken into account and impurities in the reagent alkane. Because the original reports did not include sufficient experimental details, it is not now possible to correct their results quantitatively. However, it appears, qualitatively, that the values for the O + CH₄ and O + C₂H₆ rate coefficients were overestimated by factors of approximately 2 to 3 in the 250–400 K temperature range, with the error increasing as T decreases. Although the experimental results for the O + neopentane reaction are not as sensitive to the same kinds of complications, a comparison of the low-temperature measurements with those for the O + ethane reaction suggests that the previously recommended rate coefficients, based on the data of Herron and Huie, are probably also too high by a factor of 2 to 3.