Strain measurements in and on boron-epoxy test coupons

This paper is based on an Air Force Flight Dynamics Laboratories-sponsored program to evaluate strain gages embedded in boron-epoxy test coupons. The strain gages, embedding techniques and specimen configurations used were relatively uncomplicated. The results of the program showed that the embedded-gage performance was comparable to surface-mounted-gage performance and are intended to provide a basis for more complex applications such as in joints, near holes and in sandwiched metal/fibrous composites.     

Tomonaga-Luttinger liquid and Coulomb blockade in multiwall carbon nanotubes under pressure

We report that the conductance of macroscopic multiwall nanotube (MWNT) bundles under pressure shows power laws in temperature and voltage, as corresponding to a network of bulk-bulk connected Tomonaga-Luttinger liquids (LLs). Contrary to individual MWNTs, where the observed power laws are attributed to Coulomb blockade, the measured ratio for the end and bulk obtained exponents, approximately 2.4, can be accounted for only by LL theory. At temperatures characteristic of interband separation, it increases due to thermal population of the conducting sheets unoccupied bands.     

The VIP Experimental Limit on the Pauli Exclusion Principle Violation by Electrons

In this paper we describe an experimental test of the validity of the Pauli Exclusion Principle (for electrons) which is based on a straightforward idea put forward a few years ago by Ramberg and Snow (Phys. Lett. B 238:438, 1990). We perform a very accurate search of X-rays from the Pauli-forbidden atomic transitions of electrons in the already filled 1S shells of copper atoms. Although the experiment has a very simple structure, it poses deep conceptual and interpretational problems. Here we describe the experimental method and recent experimental results, which we interpret in the framework of quon theory. We also present future plans to upgrade the experimental apparatus using Silicon Drift Detectors.     

Helical Luttinger liquid in topological insulator nanowires

We derive and analyze the effective low-energy theory for interacting electrons in a cylindrical nanowire made of a strong topological insulator. Three different approaches provide a consistent picture for the band structure, where surface states forming inside the bulk gap correspond to one-dimensional bands indexed by total angular momentum. When a half-integer magnetic flux pierces the nanowire, we find a strongly correlated helical Luttinger liquid topologically protected against weak disorder. We describe how transport experiments can detect this state.     

Nonlinear magnetotransport in interacting chiral nanotubes

Nonlinear transport through interacting single-wall nanotubes containing a few impurities is studied theoretically. Extending the Luttinger liquid theory to incorporate trigonal warping and chirality effects, we derive the current contribution Ie even in the applied voltage V and odd in an orbital magnetic field B, which is nonzero only for chiral tubes and in the presence of interactions.     

CO coordination at XNi4 clusters with impurities X = H, C, O. A density functional study

We report a computational investigation of CO adsorption on small nickel clusters that contain single impurity atoms H, C, or O. At bare Ni 4 and clusters with H or O impurity, the most stable coordination of the probe molecule is on top of a Ni atom which interacts with the impurity. The CNi 4 cluster is an exception where 3-fold coordination of CO was determined to be more stable than that on top, however, by 4 kJ/mol only. Our results suggest that the heteroatoms X (X = H, C, O) affect only weakly the reactivity of the cluster with respect to CO; the binding energy of CO in the most stable complexes (CO)XNi 4 increases at most by 10% compared to the value for bare Ni 4, 194 kJ/mol. The impurity induces a small decrease of the CO infrared frequency shift for on-top coordinated CO, compared to Ni 4, because of partial oxidation of the metal moiety. A notable difference is predicted for clusters that contain a C impurity because of the different preferred coordination mode which results in a strong CO frequency red shift of approximately 300 cm (-1). The calculated characteristic CO frequency shifts may be helpful in identifying experimentally clusters with impurity atoms.     

Density functional model studies of uranyl adsorption on (001) surfaces of kaolinite

The adsorption of uranyl on two types of neutral (001) surfaces of kaolinite, tetrahedral Si(t) and octahedral Al(o), was studied by means of density functional periodic slab model calculations. Various types of model surface complexes, adsorbed at different sites, were optimized and adsorption energies were estimated. As expected, the Si(t) surface was found to be less reactive than the Al(o) surface. At the neutral Al(o) surface, only adsorption at protonated sites is calculated to be exothermic for inner- as well as outer-sphere adsorption complexes, with monodentate coordination being preferred. Adsorption energies as well as structural features of the adsorption complexes are mainly determined by the number of deprotonated surface hydroxyl groups involved. Outer-sphere complexes on both surfaces exhibit a shorter U-O bond to the aqua ligand of uranyl that is in direct contact with the surface than to the other aqua ligands. This splitting of the shell of equatorial U-O bonds is at variance with common expectations for outer-sphere surface complexes of uranyl.     

Excretion of iodide in 24-h urine as determined by ion-pair reversed-phase liquid chromatography with electrochemical detection

A simple method is presented for the routine analysis of iodide in urine. After a one-step sample clean-up, iodide was separated by ion-pair reversed-phase liquid chromatography and detected electrochemically with a silver electrode. The coefficient of variation of a single analysis of iodide in a pooled urine sample (530 nmol/l) was 7.6%. The detection limit, derived from a signal-to-noise ratio of 3, was 3 pmol, corresponding to 0.06 mumol/l. The recovery of iodide added to urine was 96 +/- 7%. The accuracy of the method was assessed by analysing ten different samples with neutron activation analysis. The data obtained with the two methods showed a high correlation (r = 0.991) and did not differ significantly. Excretion of iodide in samples of 24-h urine from a free-living population was shown to have a log-normal distribution and to be higher in men than in women. The iodide/creatinine ratio was independent of sex and increased with age.