Physics beyond the Standard Model through b → s μ ?+? μ ? transition

A comprehensive study of the impact of new-physics operators with different Lorentz structures on decays involving the b ?? s ?? ^?+? ?? ^? transition is performed. The effects of new vector?Caxial vector (VA), scalar?Cpseudoscalar (SP) and tensor (T) interactions on the differential branching ratios, forward?Cbackward asymmetries (A _FB??s), and direct CP asymmetries of ${\bar B}_{\rm s}^0 \to \mu^+ \mu^-$ , ${\bar B}_{\rm d}^0 \to$ $ X_{\rm s} \mu^+ \mu^-$ , ${\bar B}_{\rm s}^0 \to \mu^+ \mu^- \gamma$ , ${\bar B}_{\rm d}^0 \to {\bar K} \mu^+ \mu^-$ , and ${\bar B}_{\rm d}^0\to {\bar{K}^*} \mu^+ \mu^-$ are examined. In ${\bar B}_{\rm d}^0\to {\bar{K}^*} \mu^+ \mu^-$ , we also explore the longitudinal polarization fraction f _L and the angular asymmetries $A_{\rm T}^{(2)}$ and A _LT, the direct CP asymmetries in them, as well as the triple-product CP asymmetries $A_{\rm T}^{\rm (im)}$ and $A^{\rm (im)}_{\rm LT}$ . While the new VA operators can significantly enhance most of the observables beyond the Standard Model predictions, the SP and T operators can do this only for A _FB in ${\bar B}_{\rm d}^0 \to {\bar K} \mu^+ \mu^-$ .     

Mössbauer study of magnetism in FeII − III (oxy-)hydroxycarbonate green rusts; ferrimagnetism of FeII − III hydroxycarbonate

Fe^II???III hydroxycarbonate Fe $^{\rm II}_{4}$ Fe $^{\rm III}_{2}$ (OH)₁₂CO₃, green rust GR(CO $_{3}^{2-})$ , reveals a ferrimagnetic behaviour. Moments that lie within two-dimensional cation layers are parallel for same species and antiparallel between Fe^II and Fe^III. Respective ordering temperatures are 5.2 and 7 K. A sextet with distribution from 350 to 580 kOe for Fe^III and an octet reflecting a mixture of states with field of 130 kOe and quadrupole splitting of ?3.0 mm s^???1 for Fe^II are observed at 1.4 K. Ferric oxyhydroxycarbonate Fe $^{\rm III}_{6}$ O₁₂H₈CO₃ is ferromagnetic and displays at 4 K a sextet with field between 400 and 500 kOe (maximum at 480 kOe) and transition at 80 K. GR(CO $_{3}^{2-})$ deprotonation gives magnetic domains with compositions at x?=?1/3, 2/3 and 1 due to long range order.     

Coupling constant in dispersive model

The average of the moments for event shapes in e ^?+? e??→hadrons within the context of next-to-leading order (NLO) perturbative QCD prediction in dispersive model is studied. Moments used in this article are $\langle {1-T}\rangle$ , $\langle \rho\rangle$ , $\langle {B_{\rm T}}\rangle$ and $\langle {B_{\rm W} }\rangle$ . We extract α _s, the coupling constant in perturbative theory and α ₀ in the non-perturbative theory using the dispersive model. By fitting the experimental data, the values of $\alpha_{\rm s} ({M_{\rm Z^0} })=0.1171\pm 0.00229$ and $\alpha_0 \left( {\mu_{\rm I} =2\,{\rm GeV}} \right)=0.5068\pm 0.0440$ are found. Our results are consistent with the above model. Our results are also consistent with those obtained from other experiments at different energies. All these features are explained in this paper.     

Structure of Be Hyper Isotopes

The low-lying level structure of ${^{10}_\Lambda{\rm Be}}$ and ${^{12}_\Lambda{\rm Be}}$ has been studied by using the antisymmetrized molecular dynamics for hypernuclei (HyperAMD). In these hypernuclei, it is interesting to reveal the changes of excitation spectra by adding Λ hyperon, because the ground and low-lying states with different deformation coexist in ⁹Be and ¹¹Be. Based on the HyperAMD calculation, it is found that the first excited state 1/2⁺ of ⁹Be is shifted up by about 700 keV in ${^{10}_\Lambda{\rm Be}}$ . In ${^{12}_\Lambda{\rm Be}}$ , the parity-inverted ground state of ¹¹Be is reverted by adding Λ hyperon. In this article, we discuss the reason for these structure changes related to the coexistence of ground and low-lying states with different deformation.     

Structure of some FeII − III hydroxysalt green rusts (carbonate, oxalate, methanoate) from Mössbauer spectroscopy

The abundances of Fe^II and Fe^III environments within green rusts one, GR1s, that intercalate carbonate, oxalate and methanoate (formate) anions are found from Mössbauer spectra for compositions corresponding to [Fe $^{\rm II}_{6}$ Fe $^{\rm III}_{2}$ (OH)₁₆]^2?+??[CO $_{3}^{2-}$ ?5H₂O]^2???, [Fe $^{\rm II}_{4}$ Fe $^{\rm III}_{2}$ (OH)₁₂]^2?+??[CO $_{3}^{2-}$ ?3H₂O]^2???, [Fe $^{\rm II}_{6}$ Fe $^{\rm III}_{2}$ (OH)₁₆]^2?+??[C₂O $_{4}^{2-}$ ?4H₂O]^2??? and [Fe $^{\rm II}_{5}$ Fe $^{\rm III}_{2}$ (OH)₁₄]^2?+??[2HCOO^????3H₂O]^2???. These formulae correspond to orders α, β and γ where cation distances are (2 × a ₀), ( $\surd 3$ × a ₀) or a mixture of both leading to (7 × a ₀), where ratio x = {[Fe^III]/[Fe_total]} = 1/4, 1/3 and 2/7, respectively. Anion distributions within interlayers are also devised and long-range orders determined accordingly.     

A DFG-based cavity ring-down spectrometer for trace gas sensing in the mid-infrared

Continuing studies into an all-diode laser-based 3.3 μm difference frequency generation cavity ring-down spectroscopy system are presented. Light from a 1,560 nm diode laser, amplified by an erbium-doped fibre amplifier, was mixed with 1,064 nm diode laser radiation in a bulk periodically poled lithium niobate crystal to generate 16 μW of mid-IR light at 3,346 nm with a conversion efficiency of $0.05\,\%\,{\text{W}}^{-1}\,{\text{cm}}^{-1}$ . This radiation was coupled into a 77 cm long linear cavity with average mirror reflectivities of 0.9996, and a measured baseline ring-down time of $6.07\pm 0.03\,\upmu{\rm s}$ . The potential of such a spectrometer was illustrated by investigating the $P(3)$ transition in the fundamental $\nu_{3}(F_{2})$ band of ${\text{CH}}_4$ both in a 7.5 ppmv calibrated mixture of ${\text{CH}}_4$ in air and in breath samples from methane and non-methane producers under conditions where the minimum detectable absorption coefficient ( $\alpha_{\rm min}$ ) was $2.8 \times 10^{-8}\,{\rm cm}^{-1}$ over 6 s using a ring-down time acquisition rate of 20 Hz. Allan variance measurements indicated an optimum $\alpha_{\rm min}$ of $2.9\times 10^{-9}\,{\rm cm}^{-1}$ over 44 s.     

Magnetic and Mössbauer spectra observed for mixed-metal magnets NBu4 {\bf Fe}^{\bf II}_{\bf n}MA II 1 − n [FeIII(OX)3] (MA=Mn, Fe)

Mixed-metal molecular-based magnets NBu₄ ${\rm Fe}^{\rm II}_{\rm n}$ M_A ^II _1???n[Fe^III(OX)₃] (M_A=Mn, Fe) were investigated by magnetic and Mössbauer measurements. The magnetic susceptibility of NBu₄ ${\rm Fe}^{\rm II}_{0.07}{\rm Mn}^{\rm II}_{0.93}$ [Fe^III(OX)₃] can be fitted to a Curie-Weiss law with a Weiss paramagnetic Curie temperature of θ?=??114.76 K. The negative Weiss constant indicates an intramolecular antiferromagnetic coupling interaction between the adjacent Fe(II) and Fe(III) ions through the oxalate bridge. In the complex NBu₄Fe^II[Fe^III(OX)₃], the Mössbauer results indicate that the Fe^II and Fe^III sublattices experience spontaneous magnetizations. The compound contains two different spin carriers; i.e. Fe^II(S = 2), Fe^III(S = 5/2). Two magnetic sublattices are defined. The appearance of nuclear Zeeman splittings suggests that long range magnetic ordering takes place below 50 K.     

Non-Isothermal Boundary in the Boltzmann Theory and Fourier Law

In the study of the heat transfer in the Boltzmann theory, the basic problem is to construct solutions to the following steady problem: $$v \cdot \nabla _{x}F =\frac{1}{{\rm K}_{\rm n}}Q(F,F),\qquad (x,v)\in \Omega \times \mathbf{R}^{3}, \quad \quad (0.1) $$ v · ? x F = 1 K n Q ( F , F ) , ( x , v ) ∈ Ω × R 3 , ( 0.1 ) $$F(x,v)|_{n(x)\cdot v<0} = \mu _{\theta}\int_{n(x) \cdot v^{\prime}>0}F(x,v^{\prime})(n(x)\cdot v^{\prime})dv^{\prime},\quad x \in\partial \Omega,\quad \quad (0.2) $$ F ( x , v ) | n ( x ) · v < 0 = μ θ ∫ n ( x ) · v ′ > 0 F ( x , v ′ ) ( n ( x ) · v ′ ) d v ′ , x ∈ ? Ω , ( 0.2 ) where Ω is a bounded domain in ${\mathbf{R}^{d}, 1 \leq d \leq 3}$ R d , 1 ≤ d ≤ 3 , K_n is the Knudsen number and ${\mu _{\theta}=\frac{1}{2\pi \theta ^{2}(x)} {\rm exp} [-\frac{|v|^{2}}{2\theta (x)}]}$ μ θ = 1 2 π θ 2 ( x ) exp [ - | v | 2 2 θ ( x ) ] is a Maxwellian with non-constant(non-isothermal) wall temperature θ(x). Based on new constructive coercivity estimates for both steady and dynamic cases, for ${|\theta -\theta_{0}|\leq \delta \ll 1}$ | θ - θ 0 | ≤ δ ? 1 and any fixed value of K_n, we construct a unique non-negative solution F _s to (0.1) and (0.2), continuous away from the grazing set and exponentially asymptotically stable. This solution is a genuine non-equilibrium stationary solution differing from a local equilibrium Maxwellian. As an application of our results we establish the expansion ${F_s=\mu_{\theta_0}+\delta F_{1}+O(\delta ^{2})}$ F s = μ θ 0 + δ F 1 + O ( δ 2 ) and we prove that, if the Fourier law holds, the temperature contribution associated to F ₁ must be linear, in the slab geometry.     

A Theoretical Study of Pure and Mixed Spin-Polarized Tritium and Helium Triatomic Systems Using Hyperspherical Coordinates

Pure and mixed spin-polarized tritium ( ${{\rm T}\uparrow}$ ) and helium (He) triatomic systems are studied using hyperspherical coordinates. A slow variable discretization approach is adopted to solve the nuclear Schrödinger equation, in which the Schrödinger equation in hyperangular coordinates is solved using basis splines at a series of fixed FEM-DVR hyperradii. By using the best empirical interaction potentials, we study comparatively the bound states of ( ${{\rm T}\uparrow}$ )₃, ⁴He( ${{\rm T}\uparrow}$ )₂, ${^4{\rm He}_2{\rm T}\uparrow}$ , ⁴He₃ and ${^4{\rm He}_2^3{\rm He}}$ in the J ^Π = 0⁺ symmetry. The bound state energy levels are calculated for all these molecular species except ⁴He( ${{\rm T}\uparrow}$ )₂, for which we have found no bound state. The calculated wave functions of these species are found all to exhibit a very large spatial extension, indicating the diffuse nature of these bound states. The molecular structure of these species will also be calculated and analyzed in detail.     

Alternative technique for Standard Model estimation of the rare kaon decay branchings \left. {BR(K \to \pi \nu \bar \nu )} \right|_{SM}

We estimate $BR(K \to \pi \nu \bar \nu )$ in the context of the Standard Model by fitting for λ _t≡V _tdV _ts ^* of the “kaon unitarity triangle” relation. To find the vertex of this triangle, we fit data from |? _K|, the CP-violating parameter describing K mixing, and a _ψ,K , the CP-violating asymmetry in B _d ⁰ → J/ψK ⁰ decays, and obtain the values $\left. {BR(K \to \pi \nu \bar \nu )} \right|_{SM} = (7.07 \pm 1.03) \times 10^{ - 11} $ and $\left. {BR(K_L^0 \to \pi ^0 \nu \bar \nu )} \right|_{SM} = (2.60 \pm 0.52) \times 10^{ - 11} $ . Our estimate is independent of the CKM matrix element V _cb and of the ratio of B-mixing frequencies ${{\Delta m_{B_s } } \mathord{\left/ {\vphantom {{\Delta m_{B_s } } {\Delta m_{B_d } }}} \right. \kern-0em} {\Delta m_{B_d } }}$ . We also use the constraint estimation of λ _t with additional data from $\Delta m_{B_d } $ and |V _ub|. This combined analysis slightly increases the precision of the rate estimation of $K^ + \to \pi ^ + \nu \bar \nu $ and $K_L^0 \to \pi ^0 \nu \bar \nu $ (by ?10 and ?20%, respectively). The measured value of $BR(K^ + \to \pi ^ + \nu \bar \nu )$ can be compared both to this estimate and to predictions made from ${{\Delta m_{B_s } } \mathord{\left/ {\vphantom {{\Delta m_{B_s } } {\Delta m_{B_d } }}} \right. \kern-0em} {\Delta m_{B_d } }}$ .     

\bar pp-Annihilation processes in the tree approximation of SU(3) chiral effective theory

The $\bar pp$ -annihilation reactions $\bar pp \to \eta \eta \eta$ and $\bar pp \to \eta {\rm K}\bar {\rm K}$ at rest are considered in the tree approximation in the framework of SU(3) chiral effective theory at leading order. The calculated branchings are compared with the data. The results for neutral (????, $\eta {\rm K}^0 \bar {\rm K}^0$ ) and charged (??K ⁺ K ^?) channels are essentially different.     

A Weighted Dispersive Estimate for Schrödinger Operators in Dimension Two

Let H = ?Δ + V, where V is a real valued potential on ${\mathbb {R}^2}$ satisfying ${\|V(x)|\lesssim \langle x \rangle^{-3-}}$ . We prove that if zero is a regular point of the spectrum of H = ?Δ + V, then $${\| w^{-1} e^{itH}P_{ac}f\|_{L^\infty(\mathbb{R}^2)} \lesssim \frac{1}{|t|\log^2(|t|)} \| w f\|_{L^1(\mathbb{R}^2)},\,\,\,\,\,\,\,\, |t| \geq 2}$$ , with w(x) = (log(2 + |x|))². This decay rate was obtained by Murata in the setting of weighted L ² spaces with polynomially growing weights.     

The NLS Equation in Dimension One with Spatially Concentrated Nonlinearities: the Pointlike Limit

In the present paper, we study the following scaled nonlinear Schrödinger equation (NLS) in one space dimension: $$ i\frac{\rm d}{{\rm d}t}\psi^{\varepsilon}(t)=-\Delta\psi^{\varepsilon}(t) +\frac{1}{\varepsilon}V\left(\frac{x}{\varepsilon} \right)|\psi^{\varepsilon}(t)|^{2\mu}\psi^{\varepsilon}(t)\quad \varepsilon > 0\,\quad V\in L^1(\mathbb{R},(1+|x|){\rm d}x) \cap L^\infty(\mathbb{R}).$$ This equation represents a nonlinear Schrödinger equation with a spatially concentrated nonlinearity. We show that in the limit \({\varepsilon\to 0}\) the weak (integral) dynamics converges in \({H^1(\mathbb{R})}\) to the weak dynamics of the NLS with point-concentrated nonlinearity: $$ i\frac{{\rm d}}{{\rm d}t} \psi(t) =H_{\alpha} \psi(t) .$$ where H _α is the Laplacian with the nonlinear boundary condition at the origin \({\psi'(t,0+)-\psi'(t,0-)=\alpha|\psi(t,0)|^{2\mu}\psi(t,0)}\) and \({\alpha=\int_{\mathbb{R}}V{\rm d}x}\) . The convergence occurs for every \({\mu\in \mathbb{R}^+}\) if V ≥  0 and for every  \({\mu\in (0,1)}\) otherwise. The same result holds true for a nonlinearity with an arbitrary number N of concentration points.     

Magnetic, thermal and hyperfine behaviours of Tm3+ in TmPO4, YPO4 and LuPO4: a comparative study

Single crystals of thulium phosphates (TmPO₄) are grown and the principal magnetic susceptibility perpendicular to the symmetry axis ‘c’ of the crystal $$\left( {{\text{ $ \chi $ }}_ \bot } \right)$$ and the magnetic anisotropy $$\Delta {\text{ $ \chi $ }}\left( {{\text{ = $ \chi $ }}_\parallel - {\text{ $ \chi $ }}_ \bot } \right)$$ are measured in the temperature range 300–13.5 K and 300–80 K, respectively. Though $${\text{ $ \chi $ }}_ \bot $$ increases rapidly with the decrease of temperature, $${\text{ $ \chi $ }}_\parallel $$ increases very slowly with the lowering of temperature. The tetragonal crystal structure of TmPO₄ is similar to that of Tm³⁺ in YPO₄ and LuPO₄ and in all the cases the non-Kramers Tm³⁺ ion occupies a site of D_2d symmetry. Our observed magnetic data on TmPO₄ are analyzed using crystal field analysis where the Hamiltonian includes the atomic free ion and crystal field (one-electron) interaction term. The computed and measured paramagnetic susceptibilities of TmPO₄ agree very well in the temperature range of our study. The magnetic behaviours of Tm³⁺ in YPO₄ and LuPO₄ are also studied and the results are compared with that of TmPO₄. In all the cases the natures of thermal variations of average susceptibilities and magnetic anisotropies are mostly governed by the perpendicular susceptibilities as their values are higher and rapidly increase with the lowering of temperature compared to parallel susceptibilities. The computed nuclear quadruple splittings, electronic heat capacities of Tm³⁺ in three different hosts give some interesting results.     

Muonic Anti-hydrogen {(\bar{\rm H}_{\mu}}) Formation in Low-energy Three-body Reactions

A few-body type computation is performed for a three-charge-particle collision with participation of a slow antiproton ${\bar{\rm{p}}}$ and a muonic muonium atom (true muonium), i.e. a bound state of two muons ${(\mu^{+}\mu^{-})}$ in its ground state. The total cross section of the following reaction ${\bar{\rm p}+(\mu^{+}\mu^{-}) \rightarrow \bar{\rm{H}}_{\mu} + \mu^{-}}$ , where muonic anti-hydrogen ${\bar{\rm{H}}_{\mu}=(\bar{\rm p}\mu^{+})}$ is a bound state of an antiproton and positive muon, is computed in the framework of a set of coupled two-component Faddeev-Hahn-type equation. A better known negative muon transfer low energy three-body reaction: ${{\rm t}^{+} + ({\rm d}^{+}\mu^{-})\rightarrow ({\rm t}^{+}\mu^{-}) + {\rm d}^{+}}$ is also computed as a test system. Here, t⁺ is triton and d⁺ is deuterium.     

Study of Light Hypernuclei by the (e,e′K +) Reaction

We have been performing Λ hypernuclear spectroscopic experiments by the (e,e′K ⁺) reaction since 2000 at Thomas Jefferson National Accelerator Facility (JLab). The (e,e′K ⁺) experiment can achieve a few 100 keV (FWHM) energy resolution compared to a few MeV (FWHM) by the (K ^?, π ^?) and (π ⁺, K ⁺) experiments. Therefore, more precise Λ hypernuclear structures can be investigated by the (e,e′K ⁺) experiment. ${^{7}_{\Lambda}{\rm He}}$ , ${^{9}_{\Lambda}{\rm Li}}$ , ${^{10}_{\Lambda}{\rm Be}}$ , ${^{12}_{\Lambda}{\rm B}}$ , ${^{28}_{\Lambda}{\rm Al}}$ , and ${^{52}_{\Lambda}{\rm V}}$ were measured in the experiment at JLab Hall-C. In addition, ${^{9}_{\Lambda}{\rm Li}}$ , ${^{12}_{\Lambda}{\rm B}}$ , and ${^{16}_{\Lambda}{\rm N}}$ were measured in the experiment at JLab Hall-A.     

Magnetic moment of proton halo nucleus 28 P

The magnetic moment of ²⁸P (I _π = 3^?+?, T_1/2 = 270.3 ms) in the ground state has been measured by the $\upbeta $ -nuclear magnetic resonance method for the first time. The measured magnetic moment of $\vert \upmu (^{28}$ P)∣ = 0.309(9)  $\upmu _{{\rm N}}$ is well reproduced by the shell model value of +0.306  $\upmu _{{\rm N} }$ . The shell model calculation also yields a proton density distribution with a long tail. The present results provide a strong confirmation of the configuration of the 2s _1/2 proton which should lead to the proton halo.     

The N = 16 Spherical Shell Closure in 24O

The unbound excited states of the most neutron-rich dripline oxygen isotope, ²⁴O, have been investigated by using the ²⁴O(p,p′)²⁴O^* reaction at the beam energy of 62 MeV/nucleon in inverse kinematics. The first and second unbound excited states of ²⁴O have been observed at ${E_{\rm x}= 4.63_{-0.14}^{+0.30}}$  MeV and ${E_{\rm x}= 5.13_{-0.24}^{+0.19}}$  MeV (preliminary) along with the evidence for another higher lying state at around 7.3 MeV. The quadrupole deformation parameter ${\beta_{2^+}}$ was deduced to be ${0.15_{-0.03}^{+0.08}}$ (preliminary) for the first time. The systematics of the ${\beta_{2^+}}$ and the ${E_{\rm x}(2_1^+)}$ in the Z = 8 isotopes shows the N = 16 spherical shell closure in ²⁴O.