scholarly journals Dust formation in C-star shells

1987 ◽  
Vol 122 ◽  
pp. 543-544
Author(s):  
E. Sedlmayr
Keyword(s):  
Excellent Agreement ◽  
Nucleation Theory ◽  
Classical Nucleation Theory ◽  
Condensation Temperature ◽  
Dust Formation

The formation of carbon grains is described by a chemical pathway from acetylene via polyaromatic hydrogens (PAHs). The proposed mechanism is in excellent agreement with the observations and provides in particular the observed low condensation temperature which cannot be explained by classical nucleation theory.

scholarly journals On the onset of dust formation in AGB stars

2018 ◽  
Vol 14 (S343) ◽  
pp. 119-128
Author(s):  
David Gobrecht ◽  
Stefan T. Bromley ◽  
John M. C. Plane ◽  
Leen Decin ◽  
Sergio Cristallo
Keyword(s):  
Emission Feature ◽  
Stellar Atmospheres ◽  
Nucleation Theory ◽  
Classical Nucleation Theory ◽  
Quantum Mechanical ◽  
Dust Formation ◽  
Agb Stars ◽  
Promising Candidate ◽  
Bending Modes ◽  
Structure Calculations

AbstractA promising candidate to initiate dust formation in oxygen-rich AGB stars is alumina (Al2O3) showing an emission feature around ∼13μm attributed to Al−O stretching and bending modes (Posch+99,Sloan+03). The counterpart to alumina in carbon-rich AGB atmospheres is the highly refractory silicon carbide (SiC) showing a characteristic feature around 11.3μm (Treffers74). Alumina and SiC grains are thought to represent the first condensates to emerge in AGB stellar atmospheres. We follow a bottom-up approach, starting with the smallest stoichiometric clusters (i.e. Al4O6, Si2C2), successively building up larger-sized clusters. We present new results of quantum-mechanical structure calculations of (Al2O3)n, n = 1−10 and (SiC)n clusters with n = 1−16, including potential energies, rotational constants, and structure-specific vibrational spectra. We demonstrate the energetic viability of homogeneous nucleation scenarios where monomers (Al2O3 and SiC) or dimers (Al4O6 and Si2C2) are successively added. We find significant differences between our quantum theory based results and nanoparticle properties derived from (classical) nucleation theory.

Impurity Induced Slowing oF Nucleation in Emulsified Liquids

1998 ◽  
Vol 543 ◽  
Author(s):  
Amy Herhold ◽  
Deniz Ertaş ◽  
Alex J. Levine ◽  
H. E. King
Keyword(s):  
Excellent Agreement ◽  
Careful Consideration ◽  
Nucleation Theory ◽  
Classical Nucleation Theory ◽  
Emulsion Droplet ◽  
Dynamic Generation ◽  
Liquid To Solid Transition ◽  
Kinetics Of ◽  
Existing Data

AbstractWe report detailed nucleation studies on the liquid -to -solid transition of hexadecane using nearly monodisperse hexadecane -in -water emulsions. A careful consideration of the kinetics of isothermal and nonisothermal freezing show deviations from predictions of classical nucleation theory, if one assumes that the emulsion droplet population is homogeneous. Similar deviations have been observed previously [3]. As an explanation, we propose a novel argument based on the dynamic generation of droplet heterogeneity mediated by mobile impurities. This proposal is in excellent agreement with existing data.

Twinning Stress in Fcc Metals from the Classical Nucleation Theory

2013 ◽  
Vol 658 ◽  
pp. 247-251
Author(s):  
Yan Jun Wu ◽  
Rong Zhu
Keyword(s):  
Total Energy ◽  
Excellent Agreement ◽  
Simple Form ◽  
Deformation Twinning ◽  
Nucleation Theory ◽  
Classical Nucleation Theory ◽  
Face Centered Cubic ◽  
Fcc Metals ◽  
Nucleation Barrier ◽  
Face Centered

Deformation twinning is widely observed in face-centered cubic (fcc) metals. The stress for activating twinning is an important issue to be solved. We presented an expression linking to twinning stress based on the total energy change associated with the formation of a twinning nucleus according to the classical nucleation theory. We assume there exist no energy fluctuations to overcome the nucleation barrier. The expression can predict the twinning stress for fcc metals, which is in excellent agreement with experimental results with simple form. Finally, we introduce a measure twinability to quantify the propensity of fcc metals to twin as opposed to cross-slip.

scholarly journals Phase-field modeling of grain evolutions in additive manufacturing from nucleation, growth, to coarsening

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Min Yang ◽  
Lu Wang ◽  
Wentao Yan
Keyword(s):  
Additive Manufacturing ◽  
Phase Field ◽  
Field Model ◽  
Three Dimensional ◽  
Phase Field Model ◽  
Nucleation Theory ◽  
Experimental Result ◽  
Classical Nucleation Theory ◽  
Validation Experiment ◽  
Powder Particles

AbstractA three-dimensional phase-field model is developed to simulate grain evolutions during powder-bed-fusion (PBF) additive manufacturing, while the physically-informed temperature profile is implemented from a thermal-fluid flow model. The phase-field model incorporates a nucleation model based on classical nucleation theory, as well as the initial grain structures of powder particles and substrate. The grain evolutions during the three-layer three-track PBF process are comprehensively reproduced, including grain nucleation and growth in molten pools, epitaxial growth from powder particles, substrate and previous tracks, grain re-melting and re-growth in overlapping zones, and grain coarsening in heat-affected zones. A validation experiment has been carried out, showing that the simulation results are consistent with the experimental results in the molten pool and grain morphologies. Furthermore, the grain refinement by adding nanoparticles is preliminarily reproduced and compared against the experimental result in literature.

scholarly journals On the Role of Poly-Glutamic Acid in the Early Stages of Iron(III) (Oxy)(hydr)oxide Formation

Minerals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 715
Author(s):  
Miodrag J. Lukić ◽  
Felix Lücke ◽  
Teodora Ilić ◽  
Katharina Petrović ◽  
Denis Gebauer
Keyword(s):  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Phase Separation ◽  
Fourier Transform Infrared Spectroscopy ◽  
Fourier Transform Infrared ◽  
Nucleation Theory ◽  
Classical Nucleation Theory ◽  
Oxide Formation ◽  
Early Stages ◽  
Titration Assay

Nucleation of minerals in the presence of additives is critical for achieving control over the formation of solids in biomineralization processes or during syntheses of advanced hybrid materials. Herein, we investigated the early stages of Fe(III) (oxy)(hydr)oxide formation with/without polyglutamic acid (pGlu) at low driving force for phase separation (pH 2.0 to 3.0). We employed an advanced pH-constant titration assay, X-ray diffraction, thermal analysis with mass spectrometry, Fourier Transform infrared spectroscopy, and scanning electron microscopy. Three stages were observed: initial binding, stabilization of Fe(III) pre-nucleation clusters (PNCs), and phase separation, yielding Fe(III) (oxy)(hydr)oxide. The data suggest that organic–inorganic interactions occurred via binding of olation Fe(III) PNC species. Fourier Transform Infrared Spectroscopy (FTIR) analyses revealed a plausible interaction motif and a conformational adaptation of the polypeptide. The stabilization of the aqueous Fe(III) system against nucleation by pGlu contrasts with the previously reported influence of poly-aspartic acid (pAsp). While this is difficult to explain based on classical nucleation theory, alternative notions such as the so-called PNC pathway provide a possible rationale. Developing a nucleation theory that successfully explains and predicts distinct influences for chemically similar additives like pAsp and pGlu is the Holy Grail toward advancing the knowledge of nucleation, early growth, and structure formation.

scholarly journals An Analysis of Acoustic Cavitation Thresholds of Water Based on the Incubation Time Criterion Approach

Fluids ◽  
2021 ◽  
Vol 6 (4) ◽  
pp. 134
Author(s):  
Ivan Smirnov ◽  
Natalia Mikhailova
Keyword(s):  
Incubation Time ◽  
Dynamic Strength ◽  
Acoustic Cavitation ◽  
Nucleation Theory ◽  
Classical Nucleation Theory ◽  
Accurate Estimation ◽  
Ultrasound Frequency ◽  
Time Criterion ◽  
Good Potential ◽  
Cavitation Threshold

Researchers are still working on the development of models that facilitate the accurate estimation of acoustic cavitation threshold. In this paper, we have analyzed the possibility of using the incubation time criterion to calculate the threshold of the onset of acoustic cavitation depending on the ultrasound frequency, hydrostatic pressure, and temperature of a liquid. This criterion has been successfully used by earlier studies to calculate the dynamic strength of solids and has recently been proposed in an adapted version for calculating the cavitation threshold. The analysis is carried out for various experimental data for water presented in the literature. Although the criterion assumes the use of macroparameters of a liquid, we also considered the possibility of taking into account the size of cavitation nuclei and its influence on the calculation result. We compared the results of cavitation threshold calculations done using the incubation time criterion of cavitation and the classical nucleation theory. Our results showed that the incubation time criterion more qualitatively models the results of experiments using only three parameters of the liquid. We then discussed a possible relationship between the parameters of the two approaches. The results of our study showed that the criterion under consideration has a good potential and can be conveniently used for applications where there are special requirements for ultrasound parameters, maximum negative pressure, and liquid temperature.

scholarly journals Homogeneous Freezing of Water Using Microfluidics

Micromachines ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 223
Author(s):  
Mark D. Tarn ◽  
Sebastien N. F. Sikora ◽  
Grace C. E. Porter ◽  
Jung-uk Shim ◽  
Benjamin J. Murray
Keyword(s):  
Nucleation Theory ◽  
Classical Nucleation Theory ◽  
Recent Theory ◽  
Water Droplets ◽  
Microfluidic Platforms ◽  
High Throughput Method ◽  
Theoretical Predictions ◽  
New Instrumentation ◽  
Controlled Environments ◽  
Homogeneous Freezing

The homogeneous freezing of water is important in the formation of ice in clouds, but there remains a great deal of variability in the representation of the homogeneous freezing of water in the literature. The development of new instrumentation, such as droplet microfluidic platforms, may help to constrain our understanding of the kinetics of homogeneous freezing via the analysis of monodisperse, size-selected water droplets in temporally and spatially controlled environments. Here, we evaluate droplet freezing data obtained using the Lab-on-a-Chip Nucleation by Immersed Particle Instrument (LOC-NIPI), in which droplets are generated and frozen in continuous flow. This high-throughput method was used to analyse over 16,000 water droplets (86 μm diameter) across three experimental runs, generating data with high precision and reproducibility that has largely been unrepresented in the microfluidic literature. Using this data, a new LOC-NIPI parameterisation of the volume nucleation rate coefficient (JV(T)) was determined in the temperature region of −35.1 to −36.9 °C, covering a greater JV(T) compared to most other microfluidic techniques thanks to the number of droplets analysed. Comparison to recent theory suggests inconsistencies in the theoretical representation, further implying that microfluidics could be used to inform on changes to parameterisations. By applying classical nucleation theory (CNT) to our JV(T) data, we have gone a step further than other microfluidic homogeneous freezing examples by calculating the stacking-disordered ice–supercooled water interfacial energy, estimated to be 22.5 ± 0.7 mJ m−2, again finding inconsistencies when compared to theoretical predictions. Further, we briefly review and compile all available microfluidic homogeneous freezing data in the literature, finding that the LOC-NIPI and other microfluidically generated data compare well with commonly used non-microfluidic datasets, but have generally been obtained with greater ease and with higher numbers of monodisperse droplets.

scholarly journals Low-temperature nucleation anomaly in silicate glasses shown to be artifact in a 5BaO·8SiO2 glass

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Xinsheng Xia ◽  
D. C. Van Hoesen ◽  
Matthew E. McKenzie ◽  
Randall E. Youngman ◽  
K. F. Kelton
Keyword(s):  
Nucleation Rate ◽  
Experimental Approach ◽  
Cluster Formation ◽  
Heating Time ◽  
Silicate Glasses ◽  
Nucleation Theory ◽  
Classical Nucleation Theory ◽  
Real Phenomenon ◽  
Satisfactory Answer ◽  
Over 40 Years

AbstractFor over 40 years, measurements of the nucleation rates in a large number of silicate glasses have indicated a breakdown in the Classical Nucleation Theory at temperatures below that of the peak nucleation rate. The data show that instead of steadily decreasing with decreasing temperature, the work of critical cluster formation enters a plateau and even starts to increase. Many explanations have been offered to explain this anomaly, but none have provided a satisfactory answer. We present an experimental approach to demonstrate explicitly for the example of a 5BaO ∙ 8SiO2 glass that the anomaly is not a real phenomenon, but instead an artifact arising from an insufficient heating time at low temperatures. Heating times much longer than previously used at a temperature 50 K below the peak nucleation rate temperature give results that are consistent with the predictions of the Classical Nucleation Theory. These results raise the question of whether the claimed anomaly is also an artifact in other glasses.

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