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Results for “Quadrupole”
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Quadrupole multiplet for medium energy beam transport for proton improvement plan −2
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g-factor and static quadrupole moment for the wobbling mode in 133La
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Gas-phase ion-molecule interactions in a collision reaction cell with triple quadrupole-inductively coupled plasma mass spectrometry: Investigations with N 2 O as the reaction gas
Nitrous oxide (N 2 O) was used as a reaction gas to investigate the gas phase ion-molecule interactions using the Agilent 8900 QQQ-ICP-MS. A multi-element standard containing 45 elements with masses ranging from 9 to 208 u was measured in the presence and absence of N 2 O. The main product ion species observed were oxides and nitrides. Comparison of the N 2 O reaction results with similar measurements conducted with O 2 revealed that N 2 O was more effective at forming oxides in general: the elements Cd and Pb were shown to produce oxides with N 2 O where the reaction did not occur with O 2 . Nitrous oxide was also shown to produce a significant amount of nitride species in a few cases. The general reactivity was shown to be consistent with density functional theory (DFT)-predicted reaction enthalpies, such that all predicted exothermic reactions produced product ions at levels at least 1% of the unreacted ion. Our results show that reaction enthalpy is a reasonable predictor of reactivity with N2O on the timescales of the interactions in non-thermal ICP-MS/MS systems. Our work demonstrates the utility of two relatively new platforms (commercial elemental ICP-MS/MS and EMSL Arrows interface to the NWChem program suite), which allows for the study of a large number of elements within a short period. While DFT with the basis sets utilized here is not the most accurate computational method, it is also not computationally expensive and is shown to be suitable for predicting gas phase reactivity in the QQQ-ICP-MS for the majority of ions studied. Here, the ease and rapidity of data collection and DFT calculations has the potential to be very impactful for the identification of targeted reaction chemistries to be leveraged for analytical method development, such as for the inline separation of isobaric interferences from analytes of interest.
Effect of Dynamical Motion in ab Initio Calculations of Solid-State Nuclear Magnetic and Nuclear Quadrupole Resonance Spectra
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Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry: A Strategy for Optimization, Characterization, and Quantification of Antioxidant Nitro Derivatives
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Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry Analysis of Eutectic Bis(2,2-dinitropropyl) Acetal/Formal Degradation Profile: Nontargeted Identification of Antioxidant Derivatives
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Quadrupole-mediated dielectric response and the charge-asymmetric solvation of ions in water
Treating water as a linearly responding dielectric continuum on molecular length scales allows very simple estimates of the solvation structure and thermodynamics for charged and polar solutes. While this approach can successfully account for basic length and energy scales of ion solvation, computer simulations indicate not only its quantitative inaccuracies but also its inability to capture some basic and important aspects of microscopic polarization response. Here, we consider one such shortcoming, a failure to distinguish the solvation thermodynamics of cations from that of otherwise-identical anions, and we pursue a simple, physically inspired modification of the dielectric continuum model to address it. The adaptation is motivated by analyzing the orientational response of an isolated water molecule whose dipole is rigidly constrained. Its free energy suggests a Hamiltonian for dipole fluctuations that accounts implicitly for the influence of higher-order multipole moments while respecting constraints of molecular geometry. Finally, we propose a field theory with the suggested form, whose nonlinear response breaks the charge symmetry of ion solvation. An approximate variational solution of this theory, with a single adjustable parameter, yields solvation free energies that agree closely with simulation results over a considerable range of solute size and charge.
Quadrupole strength in isobaric triplets
The dependence of the 𝐸2 matrix elements on isospin projection 𝑇 𝑧 is linked to the conservation of the isospin symmetry. To study this conjecture, we calculated the 𝐵(𝐸2 : 2 + →0 + ) rates for the even-even 𝑇=1 mirror nuclei with 42 ≤ 𝐴 ≤ 98 within nuclear density functional theory, employing the generalized Bohr Hamiltonian, and carrying out angular momentum projection. We demonstrated that collective effects are crucial for describing experimental data near the 𝑁=𝑍 line without invoking explicit beyond-Coulomb isospin symmetry-breaking corrections. We also determined the 𝐵(𝐸2↓) values for odd-odd 𝑇 𝑧 =0 nuclei 70 Br and 78 Y in doubly blocked configurations. We discussed the requirements for accurately describing isobaric analog states and emphasized how current theoretical results should be interpreted within the study of isospin symmetry across isospin triplets.
High dimensional characterization of the longitudinal phase space formed in a radio frequency quadrupole
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Nonlinear anomalous transverse responses induced by the Berry curvature quadrupole in systems with broken time-reversal symmetry
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Quadrupole and octupole collectivity in 143 Ba
The neutron-rich barium nuclei have been the subject of intense interest due to the enhanced octupole correlations they are predicted to exhibit. The observation of enhanced octupole collectivity in 144,146 Ba as measured in sub-barrier Coulomb excitation, consistent with static octupole deformation, has further heightened this interest. In the present work, these studies are extended to the neighboring odd-mass 143 Ba to investigate the interplay between single-particle and collective octupole degrees of freedom. A new measurement of the first 9/2 – -state lifetime is also presented. Reflection-Asymmetric Triaxial Particle Rotor Model calculations indicate that the negative-parity bands in 143 Ba can be understood as a decoupled structure of νh 9/2 parentage, while the positiveparity bands are built on a decoupled octupole phonon. Here, no evidence for E3 excitation is observed in this work, but an upper limit is placed on the E3 matrix element to the lowest octupole band.
Quadrupole collectivity in the neutron-rich sulfur isotopes 38,40,42,44 S
Electromagnetic transition strengths in the even-even neutron-rich sulfur isotopes 38,40,42,44 S were measured using intermediate-energy Coulomb excitation at the National Superconducting Cyclotron Laboratory. By utilizing the sensitivity of the experimental technique to E2 excitations from the ground state, the evolution of the pattern of B(E2) strengths to several low-lying 2 + states was investigated at Z = 16 from near stability to the N = 28 island of inversion. The experimental results allowed a detailed comparison with predictions from shell-model calculations using the SDPF-MU Hamiltonian, which was designed to describe collectivity in this region of the nuclear chart. While the shell-model calculations succeeded in modeling transition strengths at N = 22, 24, 26, the experimental B(E2; $0$ $^{+}_{1}$ → $2$ $^{+}_{1}$) at N = 28 was smaller than the predicted value by about a factor of 2, similar to previous observations for chlorine and argon isotopes around N = 28. The dependence of this overprediction by theory on the choice of effective charges was explored.
Quadrupole moments and proton-neutron structure in p -shell mirror nuclei
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Statistical correlations of nuclear quadrupole deformations and charge radii
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Probing the quadrupole transition strength of C 15 via deuteron inelastic scattering
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