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Results for “Thermal Diffusion”

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At least 379 records · Page 21Linked to original sources

PubMed2000

114mIn, a candidate for radionuclide therapy: low-energy cyclotron production and labeling of DTPA-D-phe-octreotide.

A method for production of carrier-free (114m)In (half-life 49.5 days), which is a potential radionuclide for radionuclide therapy of slowly growing tumors, is presented. A target consisting of five enriched cadmium ((114)Cd) foils, each 50 microm thick, was irradiated by protons (from 12.6-6.5 MeV) giving a target yield of 0. 8 MBq/microAh. A simple and cost-efficient thermal diffusion method was used for the separation. The irradiated target foils were heated for 2 h at 306 degrees C and then etched in 0.05 M HCl. The obtained cadmium/indium solution was purified using a cation ion-exchange resin (AG 1 x 8, Bio-Rad Laboratories, Hercules, CA USA). An overall yield of approximately 60% was obtained, whereas the loss of the target material was <1% per separation cycle. The (114m)In production gave (114m)In with high specific radioactivity and was successfully used to label diethylenetriamine pentaacetic acid (DTPA)-D-Phe-octreotide. Furthermore, no difference in biodistribution between [(114m)In]- and [(111)In]-DTPA-D-Phe(1)-octreotide in tumor-bearing nude mice was seen. The high radionuclide uptake in the tumors indicates a good receptor binding of the labeled octreotide.

Animals↗

PubMed2004

The 1s-state analysis applied to high-angle, annular dark-field image interpretation--when can we use it?

A small probe centered on an atomic column excites the bound and unbound states of the two-dimensional projected potential of the column. It has been argued that, even when several states are excited, only the 1s state is sufficiently localized to contribute a signal to the high-angle detector. This article shows that non-1s states do make a significant contribution for certain incident probe profiles. The contribution of the 1s state to the thermal diffuse scattering is calculated directly. Sub-Angstrom probes formed by Cs-corrected lenses excite predominantly the 1s state and contributions from other states are not very large. For probes of lower resolution when non-1s states are important, the integrated electron intensity at the column provides a better estimate of image intensity.

Image Processing, Computer-Assisted↗

PubMed2004

Direct quantification of lycopene in products derived from thermally processed tomatoes: optothermal window as a selective, sensitive, and accurate analytical method without the need for preparatory steps.

The concept of the optothermal window (OW) is proposed as a reliable analytical tool to rapidly determine the concentration of lycopene in a large variety of commercial tomato products in an extremely simple way (the determination is achieved without the need for pretreatment of the sample). The OW is a relative technique as the information is deduced from the calibration curve that relates the OW data (i.e., the product of the absorption coefficient beta and the thermal diffusion length micro) with the lycopene concentration obtained from spectrophotometric measurements. The accuracy of the method has been ascertained with a high correlation coefficient (R = 0.98) between the OW data and results acquired from the same samples by means of the conventional extraction spectrophotometric method. The intrinsic precision of the OW method is quite high (better than 1%), whereas the repeatability of the determination (RSD = 0.4-9.5%, n= 3-10) is comparable to that of spectrophotometry.

Calibration↗

PubMed2005

Ionic liquids as an attractive alternative solvent for thermal lens measurements.

The use of ionic liquids (ILs) as a solvent for thermal lens measurements has been investigated. It was found that ILs provide a better medium for thermal lens measurements than water. Specifically, not only the ILs offer at least 20 times higher sensitivity than water but that the enhancement can be appropriately adjusted by changing either the cation or the anion of the ILs. For example, the sensitivity in [BMIm]+[Tf2N]- is approximately 26 times higher than in water. It can be increased up to 31 times by changing the anion to [PF6]- (i.e., [BMIm]+[PF6]-) or to 35 times by changing the cation to [OMIm]+ (i.e., [OMIm]+[Tf2N]-). In fact, the sensitivity of thermal lens measurements in ILs is comparable to those in volatile organic solvents such as benzene, carbon tetrachloride, and hexane. However, the ILs are more desirable as they have virtually no vapor pressure. Furthermore, additional sensitivity enhancement (up to 42 times higher than that in water) can be achieved by simply adding surfactants into the ILs. Based on the thermal conductivity (k) and dn/dT values, calculated from the measured thermal time constant tc and thermal lens strength theta, it is evident that the observed sensitivity enhancement by the ILs is due to their relatively better thermooptical properties. More specifically, the enhancement is due not to the relatively modest lowering of the thermal conductivity but rather to the substantial increase in their dn/dT values. Because of the relationship between dn/dT and drho/dT, it is expected that ILs can serve as an attractive and superior solvent not only for thermal lens measurements but also for other photothermal and photoacoustic techniques as well. Also equally important is the fact that the thermal lens technique in particular and photothermal techniques, in general, can offer a unique means to determine themooptical and thermal physical properties of the ILs (e.g., thermal conductivity, thermal diffusivity, and phase transition temperatures). This type of data is currently lacking but is of extreme importance for implementing ILs as a solvent in various industrial applications.

Journal Article↗

PubMed2007

Thermal modulation voltammetry with laser heating at an aqueous|nitrobenzene solution microinterface: determination of the standard entropy changes of transfer for tetraalkylammonium ions.

Thermal modulation voltammetry (TMV) with laser heating was successfully performed at an aqueous|nitrobenzene (NB) solution microinterface, by taking advantage of the fact that laser light with a wavelength of 325.0 nm is optically transparent to the aqueous solution but opaque to the NB solution. When the laser beam impinges upon the interface from the aqueous solution side, a temperature is raised around the interface through the thermal diffusion subsequent to the light-to-heat conversion following the optical absorption by the NB solution near the interface. Based on such a principle, we achieved a fluctuating temperature perturbation around the interface for TMV by periodically irradiating the interface with the laser beam. On the other hand, the fluctuating temperature perturbation has influence on currents for transfer of an ion across the interface to produce fluctuating currents synchronized with the perturbation through temperature coefficients of several variables concerning the transfer, such as the standard transfer potential and the diffusion coefficient of the ion. Consequently, TMV has the possibility of providing information about the standard entropy change of transfer corresponding to a temperature coefficient of the standard transfer potential and a temperature coefficient of the diffusion coefficient. In this work, the aqueous|NB solution interface of 30 microm in diameter was irradiated with the laser beam at 10 Hz, and the currents synchronized with the periodical irradiation were recorded as a function of the potential difference across the interface in order to construct a TM voltammogram. TM voltammograms were measured for transfer of tetramethylammonium, tetraethylammonium, tetrapropylammonium, and tetra-n-butylammonium ions from the aqueous solution to the NB solution, and the standard entropy change of transfer was determined for each ion, according to an analytical procedure based on a mathematical expression of the TM voltammogram. Comparison of the values obtained in this work with the literature values has proved that TMV with laser heating is available for the determination of the standard entropy change of transfer for an ion.

Journal Article↗

PubMed2005

Application of transient evanescent grating techniques to the study of liquid/liquid interfaces.

Transient grating experiments performed with evanescent fields resulting from total internal reflection at an interface between a polar absorbing solution and an apolar transparent solvent are described. The time evolution of the diffracted intensity was monitored from picosecond to millisecond time scales. The diffracted signal originates essentially from two density phase gratings: one in the absorbing phase induced by thermal expansion and one in the transparent solvent due to electrostriction. A few nanoseconds after excitation, the latter grating is replaced by a thermal grating due to thermal diffusion from the absorbing phase. The speed of sound and the acoustic attenuation measured near the interface are found to be essentially the same as in the bulk solutions. However, after addition of a surfactant in the polar phase, the speed of sound near the interface differs substantially from that in the bulk with the same surfactant concentration. This effect is interpreted in terms of adsorption at the liquid/liquid interface. Other phenomena, which are not observed in bulk experiments, such as acoustic echoes and a fast oscillation of the signal intensity, are also described.

Journal Article↗

PubMed2005

Thermo-kinetics study of laser-induced desorption of self-assembled monolayers from gold: case of laser micropatterning.

Laser-induced desorption of self-assembled monolayers (SAMs) from gold surfaces within context of the direct laser patterning methodology was investigated through combining results of a heat diffusion thermal model with desorption kinetics of alkanethiol SAMs. It was found that contrast plots of experimental scanning electron microscopy (SEM) images, which are correlated to surface coverage of SAMs desorbed after laser irradiation, agreed with the theoretically predicted surface composition of SAMs. The surface composition of SAM was then interpreted in terms of the wetting property of the resulting surface. The effect of incident laser beam power and size on the final spatial coverage of SAMs on the surface and feature sizes was investigated both experimentally and by modeling. Theoretical modeling and experimental evidence showed that the resulting feature sizes are wider when the surface is heated by a laser of higher power. Increasing the laser beam size results in broadening of feature sizes. Considering the correlation of the theoretical and experimental results, we concluded that the feature sizes are controllable in a predictable way (using the presented thermal-kinetics model) through varying laser beam power and beam size.

Journal Article↗

PubMed2005

Mechanistic features for hydroxyl anion emission from the modified 12CaO.7Al2O3 surface.

OH(-), O(-), and H(-) emissions from the [Ca(24)Al(28)O(64)](4+).4(OH(-)) (defined as C12A7-OH(-)) surface were investigated by time-of-flight (TOF) spectrometry. The emission intensities were sensitive to surface temperature and extraction field. The apparent activation energies of anions decreased with the increase of applied extraction field. At an extraction field of 800 V/cm, the emission ratio of OH(-) to total anions is 0.98-0.65 in the temperature range of 870-1075 K. The OH(-) emission from C12A7-OH(-) was described by the following kinetic processes: the OH(-) anions in the cages migrated onto the sample surface by field enhanced thermal diffusion, and then desorbed to form the gas-phase anions of OH(-). The O(-) emission originated from the dissociation of O(2-) and OH(-). Similarly, H(-) emission was also attributed to the dissociation of OH(-) on the C12A7-OH(-) surface.

Aluminum Oxide↗

PubMed2005

Time evolution of density fluctuation in the supercritical region. 2. Comparison of hydrogen- and non-hydrogen-bonded fluids.

The time evolution of the density fluctuation of molecules is investigated by dynamic light scattering in six neat fluids in supercritical states. This study is the first to compare the dynamics of density inhomogeneity between hydrogen- and non-hydrogen-bonded fluids. Supercritical methanol and ethanol are used as hydrogen-bonded fluids, whereas four non-hydrogen-bonded fluids were used: CHF(3), C(2)H(4), CO(2), and Xe. We measure the time correlation function of the density fluctuation of each fluid at the same reduced temperatures and densities and investigate the relationship between the dynamic and static density inhomogeneities of those supercritical fluids. In all cases, the profile of the time correlation function of the density fluctuation is characterized by a single-exponential function, whose decay is responsible for the dynamics characterized by hydrodynamic conditions. We obtain correlation times from the time correlation function and discuss dynamic and static inhomogeneity using the Kawasaki theory and the Landau-Placzek theory. While the correlation times in the six fluids show noncoincidence, those values agree well with each other except for the supercritical alcohols when scaled to a dimensionless parameter. Although the principle of corresponding state is observed in the non-hydrogen-bonded fluids, both the supercritical methanol and ethanol deviate from that principle. This deviation is attributed to the presence of hydrogen bonding among alcohol molecules at high temperature and low density. The average cluster size of each fluid is estimated under the same thermodynamic conditions, and it is shown that the clusters of supercritical alcohols are on average 1.5-1.7 times larger than those of the four non-hydrogen-bonded fluids. Moreover, the thermal diffusivity of each neat fluid is obtained over wide ranges of density and temperature.

Journal Article↗

PubMed2005

Gold atoms and dimers on amorphous SiO(2): calculation of optical properties and cavity ringdown spectroscopy measurements.

We report on the optical absorption spectra of gold atoms and dimers deposited on amorphous silica in size-selected fashion. Experimental spectra were obtained by cavity ringdown spectroscopy. Issues on soft-landing, fragmentation, and thermal diffusion are discussed on the basis of the experimental results. In parallel, cluster and periodic supercell density functional theory (DFT) calculations were performed to model atoms and dimers trapped on various defect sites of amorphous silica. Optically allowed electronic transitions were calculated, and comparisons with the experimental spectra show that silicon dangling bonds [[triple bond]Si(.-)], nonbridging oxygen [[triple bond]Si-O(.-)], and the silanolate group [[triple bond]Si-O(-)] act as trapping centers for the gold particles. The results are not only important for understanding the chemical bonding of atoms and clusters on oxide surfaces, but they will also be of fundamental interest for photochemical studies of size-selected clusters on surfaces.

Journal Article↗

PubMed2001

Recombination reduction of photooxidized cytochrome c in reaction centers of Rhodopseudomonas viridis at low temperature.

The temperature dependence of dark reduction of photooxidized cytochrome c was studied in isolated preparations of Rhodopseudomonas viridis reaction centers. Within the range from room temperature to approximately 260 K this process was found to be mediated by thermal diffusion of exogenous donor molecules, whereas at lower temperatures photooxidized cytochrome is reduced as a result of indirect recombination with photoreduced primary quinone acceptor. Kinetic simulation allowed certain thermodynamic characteristics of this reaction to be calculated. To the first approximation, these characteristics correlate with the estimates obtained from the results of direct redox titration.

Benzoquinones↗

PubMed1997

In-situ polymerization behaviour of bone cements.

The polymerization behaviour of bone cements during total hip replacements is characterized by a fast and highly non-isothermal bulk reaction. In the first part of this paper the reaction kinetics are analysed by calorimetric analysis in order to determine the rates of polymerization in isothermal and non-isothermal conditions. A phenomenological kinetic model, accounting for the effects of autoacceleration and vitrification, is presented. This model, integrated with an energy balance, is capable of predicting the temperature across the prosthesis, the cement and the bone and the degree of reaction in the cement, during in situ polymerization. The temperature and the degree of reaction profiles are calculated, as a function of the setting time, taking into account the system geometry, the thermal diffusivity of bone, prosthesis and cement, and the heat rate generated by the reaction according to the kinetic model. Material properties, boundary and initial conditions are the input data of the heat transfer model. Kinetic and heat transfer models are coupled and a numerical solution method is used. The model is applied in order to study the effects of different application procedures on temperature and degree of reaction profiles across the bone-cement-prosthesis system.

Journal Article↗

PubMed1990

A numerical simulation of climate changes during the obliquity cycle on Mars.

A one-dimensional seasonal energy balance climate model has been developed for the Martian surface and coupled to a model of CO2 distribution between atmosphere, regolith, and polar caps. This model takes into account the greenhouse warming of carbon dioxide, the meridional transport of heat, the CO2 condensation and sublimation cycle, and its adsorption in the regolith. The model takes into consideration the diurnal variation of solar irradiation, since it is shown that disregard of this effect yields temperatures too high by several degrees. The yearly-averaged temperatures calculated from this climate model at different obliquities are used to estimate the importance of CO2 exchanges between the regolith and atmosphere-cap systems during the obliquity cycle. For this purpose, the equation of thermal diffusion into the ground is solved for each latitude belt. The results differ substantially from those of previous studies, due in part to the consideration of the diurnal and seasonal variations of the solar irradiance. The model shows the importance of taking these short-period variations into account instead of using yearly-averaged quantities, due to the strong nonlinearity of the climate system on Mars. The roles of meridional heat transport and greenhouse warming are analyzed and shown to be important. For example, a permanent polar cap of carbon dioxide is destroyed by heat transport when the obliquity is high, while at low obliquity, high-pressure systems without permanent cap can exist if enough exchangeable carbon dioxide is available. Further, the results show the possible existence of hysteresis cycles in the formation and sublimation of permanent deposits during the course of the obliquity cycle.

Atmosphere↗

PubMed2000

The initiation and characterization of single bimolecular reactions with a scanning tunneling microscope.

A scanning tunneling microscope (STM) operating at 9 K in ultrahigh vacuum was used to initiate a bimolecular reaction between isolated hydrogen sulfide and dicarbon molecules on the Cu(001) surface. The reaction products ethynyl (CCH) and sulfhydryl (SH) were identified by inelastic electron tunneling spectroscopy (STM-IETS) and by sequentially removing hydrogen atoms from an H2S molecule using energetic tunneling electrons. For comparison, the thermal diffusion and reaction of H2S and CC at 45 K and H2O and CC at 9 K were also observed.

Journal Article↗

PubMed2006

Single molecule sensitivity in SERS: importance of junction of adjacent Ag nanoparticles.

An enormous SERS (Surface Enhanced Raman Scattering) signal from dye and adenine on hot or blinking silver nanoparticles is extinguished by duration of measurement possibly due to thermal diffusion or desorption of adsorbed molecules. Simultaneously, the elastic scattering peak at ca. 630 nm disappears. The Three-dimensional Finite Difference Time Domain (FDTD-3D) method manifests this scattering peak as originating from enhanced coupling of localized surface plasmon (LSP) on adjacent Ag particles through absorption of adspecies located at their junction. Distinct emission peaks were observed at 550-600 nm and 600-750 nm. Based on the spectral variations for different surface coverage and for different dye species, the shorter and longer wavelength peaks were attributed to excited electrons on metal, and from fluorescence of molecules, respectively. Furthermore, we found the shorter wavelength peak shows invariant Stokes shift irrespective of excitation wavelengths, indicating it arises from inelastic scattering of excited electron by surface roughness or by adsorbed molecules.

Journal Article↗

PubMed2005

On the temperature stability of gold nanorods: comparison between thermal and ultrafast laser-induced heating.

The response of gold nanorods to both thermal and ultrafast laser-induced heating has been examined. The thermal heating experiments show structural changes that occur on timescales ranging from hours to days. At the highest temperature examined (250 degrees C) the nanorods are transformed into spheres within an hour. On the other hand, no structural changes are observed in the laser-induced heating experiments up to temperatures of 700 +/- 50 degrees C. This is attributed to thermal diffusion in the laser experiments. Measurements of the period of the extensional mode of the nanorods using time-resolved spectroscopy show a significant softening at high pump laser powers. However, the decrease in the period is less than expected from bulk Young's modulus vs. temperature data.

Journal Article↗

PubMed2004

Continuous and real-time blood perfusion monitoring in prefabricated flaps.

The Thermal Diffusion Probe (TDP) System allows continuous real-time measurement of tissue perfusion in flaps. The authors used a TDP with two thermistors, one active, the other passive, embedded in a 0.9-mm diameter catheter to measure continuous tissue perfusion in rabbit epigastric flaps. The distal thermistor is heated to 2 degrees C above the tissue baseline temperature. The power required to maintain this temperature difference is mathematically related to the tissue perfusion in the volume surrounding the probe tip. Central and peripheral TDPs were placed. The TDP effectiveness in detecting and measuring daily tissue perfusion in buried epigastric flaps was tested. Contralateral epigastric pedicles were transposed into the flaps prior to ligation of the original pedicle. Flaps with transposed pedicles showed a progressive and significant increase in tissue perfusion during the initial 3 weeks of the experiment, compared to flaps without the pedicle transfer. The TDP System is a useful experimental method for the continuous and real-time quantification of flap perfusion and may be helpful in making clinical decisions about prefabricated flap transfer.

Animals↗

PubMed2004

Thermodiffusion of interacting colloids. I. A statistical thermodynamics approach.

The thermal diffusion coefficient of colloids consists of two additive contributions, one related to specific interactions between the surfaces of colloidal particles with solvent molecules, and a contribution due to interactions between the colloidal particles. In the present paper, the effect of intercolloidal particle interactions on their thermodiffusive behavior is discussed within a statistical thermodynamics framework. Transport coefficients are expressed in terms of the interaction potential between the colloidal spheres. A special feature of macromolecular systems is that this interaction potential is a potential of mean force, which is temperature dependent. It is shown that under certain conditions this implicit temperature dependence gives rise to negative Soret coefficients, that is, to diffusion of macromolecules to hot regions.

Journal Article↗