Measurement of storage time, estimation of ion number and study of absorption line profile in a Paul trap

Europium (Eu⁺) ions were confined in a Paul trap and detected by non-destructive method. Storage time of Eu⁺ ions achieved in vacuum was improved by orders of magnitude employing buffer gas cooling. The experimentally detected signal was fitted to the ion response signal and the total number of ions trapped was estimated. It is found that the peak signal amplitude as well as the product of FWHM and the peak signal amplitude is proportional to the total number of trapped ions. The trapped ion secular frequency was swept at different rates and its effect on the absorption line profile was studied both experimentally and theoretically.     

A vacuum exterior to Maitra’s cylindrical dust solution

Maitra’s shearing, rotating cylindrical dust solution is fitted to a vacuum exterior. There are no closed timelike curves in the interior or exterior.     

Correction: Dermatan sulfate in tunicate phylogeny: Order-specific sulfation pattern and the effect of [→4IdoA(2-Sulfate)β-1→3GalNAc(4-Sulfate)β-1→] motifs in dermatan sulfate on heparin cofactor II activity

After the publication of the work entitled "Dermatan sulfate in tunicate phylogeny: Order-specific sulfation pattern and the effect of [→4IdoA(2-Sulfate)β-1→3GalNAc(4-Sulfate)β-1→] motifs in dermatan sulfate on heparin cofactor II activity", by Kozlowski et al., BMC Biochemistry 2011, 12:29, we found that the legends to Figures 2 to 5 contain serious mistakes that compromise the comprehension of the work. This correction article contains the correct text of the legends to Figures 2 to 5.     

Measurements ofE4 matrix elements in152Sm and154Sm

TheE4 transition matrix element from the ground state to the 4⁺ state has been measured in¹⁵²Sm and¹⁵⁴Sm, by comparing relative thick targetγ-ray intensities following Coulomb excitation with 12 MeV⁴He, 24–30 MeV¹⁶O, and 35–40 MeV³²S projectiles. Values for 〈0⁺∥?(E4)∥4⁺〉 of (+0.31 _?0.20 ^+0.12 ) barn in¹⁵²Sm and (+0.50 _?0.12 ^+0.09 ) barn in¹⁵⁴Sm are found.     

On the feasibility of using thermal gradients for active control of interlaminar stresses in laminated composites

In this paper, a method is proposed to actively control interlaminar stresses near the free edges of laminated composites by though-thickness thermal gradients. Theoretical solutions are given for optimal steady-state through-thickness temperature distributions under uniaxial loading that are required to eliminate or reduce the interlaminar stresses below a prescribed level. The optimal solutions are obtained by minimizing appropriate performance indices that are functions of the far-field properties, with respect to the through-thickness temperature differences. In the second part, an experimental investigation is conducted on a glass/epoxy cross-ply laminate with embedded piezoelectric sensors and a thermal heater. Through the experiment, the feasibility of the thermal control of interlaminar stresses is demonstrated.     

Investigating the reaction mechanism and organocatalytic synthesis of α,α'-dihydroxy ketones

A biomimetic TK one-pot reaction using hydroxypyruvate and aldehydes to generate α,α'-dihydroxy ketones in water has recently been described. To investigate this tertiary-amine mediated reaction mechanism two approaches were used. Firstly, (13)C labelled lithium hydroxypyruvate was synthesised and used to establish where hydroxypyruvate is incorporated in the product. In separate experiments reaction intermediates were also successfully intercepted and structurally identified using ESI-MS with tandem mass spectrometry ESI-MS/MS. These studies indicated that two mechanisms appear to be operating, one involving the addition of the tertiary amine catalyst to hydroxypyruvate, the other an aldol-based mechanism. Since the first mechanism may enable facial stereodifferentiation in the addition of intermediates to the aldehyde, a preliminary study on the use of chiral catalysts was performed and the first asymmetric organocatalytic synthesis of α,α'-dihydroxy ketones in aqueous media achieved, in up to 50% ee, using a quinine ether catalyst.