Role of stress in thin film alloy thermodynamics: competition between alloying and dislocation formation

Using scanning tunneling microscopy (STM) and first-principles local-spin-density-approximation calculations to study submonolayer films of Co (1-c)Ag (c)/Ru(0001) alloys, we have discovered a novel phase-separation mechanism. When the Ag concentration c exceeds 0.4, the surface phase separates between a dislocated, pure Ag phase and a pseudomorphically strained Co(0.6)Ag (0.4) surface alloy. We attribute the phase separation to the competition between two stress relief mechanisms: surface alloying and dislocation formation. The agreement between STM measurements and our calculated phase diagram supports this interpretation.     

Sonoelastographic imaging of interference patterns for estimation of shear velocity distribution in biomaterials

The authors have recently demonstrated the shear wave interference patterns created by two coherent vibration sources imaged with the vibration sonoelastography technique. If the two sources vibrate at slightly different frequencies omega and omega+deltaomega, respectively, the interference patterns move at an apparent velocity of (deltaomega/2omega)upsilon(shear), where upsilon(shear) is the shear wave speed. We name the moving interference patterns "crawling waves." In this paper, we extend the techniques to inspect biomaterials with nonuniform stiffness distributions. A relationship between the local crawling wave speed and the local shear wave velocity is derived. In addition, a modified technique is proposed whereby only one shear wave source propagates shear waves into the medium at the frequency omega. The ultrasound probe is externally vibrated at the frequency omega-deltaomega. The resulting field estimated by the ultrasound (US) scanner is proven to be an exact representation of the propagating shear wave field. The authors name the apparent wave motion "holography waves." Real-time video sequences of both types of waves are acquired on various inhomogeneous elastic media. The distribution of the crawling/holographic wave speeds are estimated. The estimated wave speeds correlate with the stiffness distributions.     

Early assessment of breast cancer response to neoadjuvant chemotherapy by semi-quantitative analysis of high-temporal resolution DCE-MRI: Preliminary results

Purpose

To evaluate whether semi-quantitative analysis of high temporal resolution dynamic contrast-enhanced MRI (DCE-MRI) acquired early in treatment can predict the response of locally advanced breast cancer (LABC) to neoadjuvant chemotherapy (NAC).

Materials and Methods

As part of an IRB-approved prospective study, 21 patients with LABC provided informed consent and underwent high temporal resolution 3 T DCE-MRI before and after 1 cycle of NAC. Using measurements performed by two radiologists, the following parameters were extracted for lesions at both examinations: lesion size (short and long axes, in both early and late phases of enhancement), radiologist's subjective assessment of lesion enhancement, and percentages of voxels within the lesion demonstrating progressive, plateau, or washout kinetics. The latter data were calculated using two filters, one selecting for voxels enhancing ≥ 50% over baseline and one for voxels enhancing ≥ 100% over baseline. Pretreatment imaging parameters and parameter changes following cycle 1 of NAC were evaluated for their ability to discriminate patients with an eventual pathological complete response (pCR).

Results

All 21 patients completed NAC followed by surgery, with 9 patients achieving a pCR. No pretreatment imaging parameters were predictive of pCR. However, change after cycle 1 of NAC in percentage of voxels demonstrating washout kinetics with a 100% enhancement filter discriminated patients with an eventual pCR with an area under the receiver operating characteristic curve (AUC) of 0.77. Changes in other parameters, including lesion size, did not predict pCR.

Conclusion

Semi-quantitative analysis of high temporal resolution DCE-MRI in patients with LABC can discriminate patients with an eventual pCR after one cycle of NAC.     

Determination of streptomycin in pharmaceutical preparations by gas chromatography

The antibiotic streptomycin can be reliably quantitated in injectable pharmaceuticals by GC. The manipulations are not difficult, and total analysis time for duplicate samples is less than twenty minutes. Reaction of the drug with aqueous sodium hydroxide solution generates maltol, which is extracted into chloroform prior to silylation. The silyl ether of maltol is then assayed, using naphthalene as internal standard. Duplicate analyses of twenty pharmaceutical samples showed a relative standard deviation of ±1.3%.     

Three-dimensional visualization of large structures in the turbulent boundary layer

 A new method of visualizing the coherent structures in the boundary layer is used to develop insight into how these structures form and to provide information on the relative frequency of typical shapes noticed in the near-wall flow. These results were achieved in a water channel using a recently developed tracer which remains as a moving dye streak while conforming to the convoluted motions in the boundary layer. The tracer is formulated from a surfactant–polymer–emulsion mixture which retains its capabilities as a marker of evolving flow motions in the boundary layer for a meter or more before eventually dispersing. Three-dimensional, continuous visualization of the structures can be obtained as they move along a flat plate. Photos and video frames demonstrate the evolution and properties of the most widely discussed boundary-layer structure, the Theodorsen (horseshoe) vortex. Received: 16 November 1999/Accepted: 24 May 2000     

Atomistic Simulation Methods for Computing the Kinetic Coefficient in Solid-Liquid Systems

The kinetic coefficient, , is the constant of proportionality between the velocity of a solid-liquid interface and the interface undercooling. The value of and its anisotropy are critical parameters in phase field modeling of dendritic solidification. In this paper we review several different molecular dynamics simulation methods which have been proposed to compute the kinetic coefficient. Techniques based on forced velocity simulations, free solidification simulations and fluctuation analyses are discussed and compared. In addition, a model of crystalline growth kinetics due to Broughton, Gilmer and Jackson will be compared with available atomistic simulation data.     

Comments on "Two-mass models of the vocal cords for natural sounding voice synthesis"

Koizumi et al. [J. Acoust. Soc. Am. 82, 1179-1192 (1987)] have proposed a way to incorporate mucosal waves into previous two-mass mechanical models of the vocal folds. This was accomplished by allowing the mass of the masses to vary with time. The equations of motion Koizumi et al. used to mathematically describe this model neglected terms from the time rate of change of momentum of Newton's second law. In this letter, approximations of the magnitude of this term indicate that it must not be neglected.     

C-H bond activation of hydrocarbons by an imidozirconocene complex

Monomeric imidozirconocene complexes of the type Cp2(L)Zr=NCMe3 (Cp = cyclopentadienyl, L = Lewis base) have been shown to activate the carbon-hydrogen bonds of benzene, but not the C-H bonds of saturated hydrocarbons. To our knowledge, this singularly important class of C-H activation reactions has heretofore not been observed in imidometallocene systems. The M=NR bond formed on heating the racemic ethylenebis(tetrahydro)indenyl methyl tert-butyl amide complex, however, cleanly and quantitatively activates a wide range of n-alkane, alkene, and arene C-H bonds. Mechanistic experiments support the proposal of intramolecular elimination of methane followed by a concerted addition of the hydrocarbon C-H bond. Products formed by activation of sp2 C-H bonds are generally more thermodynamically stable than those formed by activation of sp3 C-H bonds, and those resulting from reaction at primary C-H bonds are preferred over secondary sp3 C-H activation products. There is also evidence that thermodynamic selectivity among C-H bonds is sterically rather than electronically controlled.