Investigations of two-level tunneling systems in n-irradiated quartz by diffuse x-ray scattering

Abstract

Recent observation of the acoustic saturation and of phonon echoes in crystalline quartz after light irradiation with fast neutrons indicates that there are the same low-energy atomic tunnelling systems as in Si0₂ glass.

We report measurements of the diffuse X-ray scattering and of the lattice parameter change from neutron irradiated quartz single crystals studying the strength and symmetry of strain defects and their local correlations. For dose 3 × 10¹⁸ n/cm² the diffuse scattering close to the Bragg peaks together with the lattice parameter change shows that the neutrons create defective regions with a volume change of 29 mean atomic volumes. The distortion field of these regions shows no high symmetry. The radius of the heavily strained region is ～ 10 Å. For higher doses the regions grow a little bit but mainly new defective regions are built.

According to the various volume fractions of defective regions at various doses the first strong amorphous halo at about K≈ 1.5 A^?1 was detected. Since this amorphous scattering is isotropic and during annealing the regions disappear mainly without changing their size we are led to the conclusion that the defective regions are glass-like in nature. So the size of the tunnelling system has to be smaller than 20 Å.     

Ultrahigh pressure equation of state of tantalum to 310 GPa

ABSTRACT

The isothermal compression of transition metal tantalum (Ta) was studied in a diamond anvil cell by X-ray diffraction utilizing rhenium (Re) and gold (Au) as internal X-ray pressure standards. The Re pressure marker was employed during non-hydrostatic compression to pressures up to 310?GPa while the Au pressure marker was used during quasi-hydrostatic compression in a neon pressure-transmitting medium to 80?GPa. Two ultra-high pressure experiments were conducted on Ta and Re mixtures utilizing focused-ion beam machined toroidal diamond anvils with central flats varying from 8 microns to 16 microns in diameter. The Ta metal was observed to be stable in the body-centered-cubic phase to a volume compression V/V₀?=?0.581. The measured equations of state (EOS) of Ta using two different calibrations of the Re pressure marker are compared with the ambient temperature isotherm derived from shock compression data. We provide a detailed analysis of EOS fit parameters for Ta under quasi-hydrostatic and non-hydrostatic conditions.     

Ultrafast spectroscopic study of the photochemistry and photophysics of arylhalodiazirines: direct observation of carbene and zwitterion formation

Ultrafast photolysis (lambdaex = 270, 350, or 360 nm) of bromophenyl, chlorophenyl, fluorophenyl, and fluoro-para-trifluoromethylphenyl diazirines produces transient species which absorb broadly in the UV and visible regions. Transient decay can be fit to either mono- or biexponential functions (tau1 approximately 0.3-10 ps, tau2 approximately 10-350 ps; dependent on solvent and halogen). Fluoro- and chlorophenylcarbene are formed within the time resolution of the spectrometer (300 fs, 270 nm excitation). Bromophenyl diazirine decay (270 nm excitation) correlates with the growth of bromophenylcarbene. Solvent and substituent effects on the slower decays of the transient absorptions are consistent with assigning the carriers of transient absorption in the visible region to ring-opened zwitterionic species.     

Transient innermolecular carbene-hemicarcerand complex of fluorophenylcarbene

Laser flash photolysis of fluorophenyldiazirine incarcerated in hemicarcerand 2 affords incarcerated fluorophenylcarbene [2⊙3], which forms a metastable, innermolecular π-complex with aryl moieties of 2. This carbene complex can be observed spectroscopically. Extensive computational studies provide insights into the structure, spectroscopy, energetics, and kinetics of the 2⊙3 carbene complex.     

Differentiation of electrophilic and ambiphilic carbenes

Comparative selectivities toward alkenes of CH₃CCl, CCl₂, and CH₃OCCl establish the former two carbenes as electrophiles; the latter is an ambiphile.     

Development of high efficiency, multi-element CdZnTe detectors for portable measurement applications

We describe the development of detector arrays and electronics for large-volume, hand-held CdZnTe detectors with the same counting efficiency as portable NaI(Tl) detectors presently used for nuclear material measurement applications. The pulse-height resolution of the multi-element detectors is at least three times better than NaI(Tl) over a wide energy range (from 100 keV to several MeV), enabling more accurate measurements of gamma-rays emitted by special nuclear material. Arrays of up to eight coplanar grid detectors can be combined to make detectors ranging in size from 4 to 14 cm³. Because the number of spectroscopy channels is small, low-power, hand-held detectors can be manufactured with conventional printed circuit board technology, thus keeping the cost of multi-element detectors to a minimum. The design and performance of an 8-element detector is presented.     

Quantitative Impact of a Cognitive Modeling Intelligent Tutoring System on Student Performance in Balancing Chemical Equations

The need for improved interactive tutoring capabilities in educational software for chemistry problem solving is an important one clearly articulated by teachers and students. To deliver the next generation of individualized interactive capabilities users demand, it is necessary to go beyond the conventional computer-assisted instruction methodology. The focus of this paper is the assessment with first-semester general chemistry students of a recently developed artificial intelligence (AI) tutor for balancing chemical equations. This is the first such assessment of an AI-based learning tool in chemistry. Students in CHEM 121 in the Fall 2001 semester at Duquesne University (N = 273) participated in the study. Students were divided into a test group that used the AI tutor as part of their study activities and a control group that did not use the tutor. It was found that the tutor improved the performance of the test group students to a statistically significant degree, helping the weakest students the most. This study establishes the feasibility of an AI-based approach to creating advanced new tutoring software for chemistry problem solving. Access to a Web-based demonstration of the equation-balancing tutor may be obtained by emailing the corresponding author.     

Development of an information-intensive structure–activity relationship model and its application to human respiratory chemical sensitizers

Structure–activity relationship (SAR) models are recognized as powerful tools to predict the toxicologic potential of new or untested chemicals and also provide insight into possible mechanisms of toxicity. Models have been based on physicochemical attributes and structural features of chemicals. We describe herein the development of a new SAR modeling algorithm called cat-SAR that is capable of analyzing and predicting chemical activity from divergent biological response data. The cat-SAR program develops chemical fragment-based SAR models from categorical biological response data (e.g. toxicologically active and inactive compounds). The database selected for model development was a published set of chemicals documented to cause respiratory hypersensitivity in humans. Two models were generated that differed only in that one model included explicate hydrogen containing fragments. The predictive abilities of the models were tested using leave-one-out cross-validation tests. One model had a sensitivity of 0.94 and specificity of 0.87 yielding an overall correct prediction of 91%. The second model had a sensitivity of 0.89, specificity of 0.95 and overall correct prediction of 92%. The demonstrated predictive capabilities of the cat-SAR approach, together with its modeling flexibility and design transparency, suggest the potential for its widespread applicability to toxicity prediction and for deriving mechanistic insight into toxicologic effects.     

Rhodium catalysed tandem conjugate addition-protonation: an enantioselective synthesis of 2-substituted succinic esters

The rhodium catalysed addition of potassium trifluoro(organo)borates to dimethyl itaconate generates an intermediate complex which on protonation provides enantioenriched succinic esters.