Slotted Rotatable Target Assembley and Systematic Error Analysis for a Search for Long Range Spin Dependent Interactions from Exotic Vector Boson Exchange Using Neutron Spin Rotation

We discuss the design and construction of a novel target array of nonmagnetic test masses used in a neutron polarimetry measurement made in search for new possible exotic spin dependent neutron–atominteractions of Nature at sub-mm length scales. This target was designed to accept and efficiently transmit a transversely polarized slow neutron beam through a series of long open parallel slots bounded by flat rectangular plates. These openings possessed equal atom density gradients normal to the slots from the flat test masses with dimensions optimized to achieve maximum sensitivity to an exotic spin-dependent interaction from vector boson exchanges with ranges in the mm - μm regime. The parallel slots were oriented differently in four quadrants that can be rotated about the neutron beam axis in discrete 90°increments using a Geneva drive. The spin rotation signals from the 4 quadrants were measured using a segmented neutron ion chamber to suppress possible systematic errors from stray magnetic fields in the target region. We discuss the per-neutron sensitivity of the target to the exotic interaction, the design constraints, the potential sources of systematic errors which could be present in this design, and our estimate of the achievable sensitivity using this method

A Search for Possible Long Range Spin Dependent Interactions of the Neutron from Exotic Vector Boson Exchange

We present a search for possible spin dependent interactions of the neutron with matter through exchange of spin 1 bosons with axial vector couplings as envisioned in possible extensions of the Standard Model. This was sought using a slow neutron polarimeter that passed transversely polarized slow neutrons by unpolarized slabs of material arranged so that interactions would tilt the plane of polarization and develop a component along the neutron momentum. The result for the rotation angle, ϕ′=[2.8±4.6(stat.)±4.0(sys.)]×10−5 rad/m is consistent with zero. This result improves the upper bounds on the neutron-matter coupling g2A by about three orders of magnitude for force ranges in the mm– μm regime

The Association between Smoking and Ectopic Pregnancy:Why Nicotine Is BAD for Your Fallopian Tube

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Testicular Cancer: Contemporary Updates in Staging

Testicular tumors are the most common solid tumors in young men, the vast majority of which are of germ cell origin. The staging of human cancers is paramount to correct patient management. Staging systems have passed through several developments leading to the release of the most recent 8th edition of the American Joint Committee for Cancer (AJCC) staging manual, which is based on the current understanding of tumor behavior and spread. In this review, the authors summarize the current AJCC staging of the germ cell tumors, highlight essential concepts, and provide insight into the most important parameters of testicular tumors

Dipole moment of the HOOO radical: resolution of a structural enigma

A global six-dimensional potential surface for the hydridotrioxygen radical (HOOO) is needed for an accurate assessment of its atmospheric abundance. We report inertial dipole moment components obtained from Stark spectra of the trans-HOOO system solvated in superfluid helium, and these are shown to be stringent benchmarks for theoretical computations of the potential surface. Computed dipole moment components at the CCSD(T)/CBS equilibrium geometry disagree qualitatively with the experimental values. The role of large-amplitude motion and vibrational averaging is assessed by computing the ground-state wave function on a relaxed, two-dimensional potential surface for the HO1O2O3 torsional and O1O2 bond-stretching coordinates. The experimental and computed vibrationally averaged dipole moments agree only after shifting the potential along the O1O2 bond coordinate, indicating that single-reference CCSD(T)/CBS computations underestimate re(O1O2) by ∼0.08 Å. An optimized trans-HOOO geometry at the composite all-electron CCSDT(Q)/CBS level reveals that the inclusion of full triples and a perturbative treatment of quadruple excitations leads to an increase in re(O1O2) by 0.07 Å.Tao Liang, D. Brandon Magers, Paul L. Raston, Wesley D. Allen, and Gary E. Douberl

Investigation of the Precipitation Behavior of Asphaltenes in the Presence of Naphthenic Acids Using Light Scattering and Molecular Modeling Techniques

A delay in the onset of flocculation is observed for asphaltenes in the presence of several naphthenic acids: methyl abietate, hydrogenated methyl abietate, 5β-cholanic acid, and 5β-cholanic acid-3-one. This flocculation behavior is monitored as a function of the added precipitant (n-heptane) to solutions of suspended asphaltenes and naphthenic acids in model solutions of toluene/n-heptane, using a combination of dynamic light scattering (DLS) and near-infrared (NIR) spectroscopic techniques. DLS and NIR show very good correlation in indentifying the onsets of flocculation, which varied among the series of naphthenic acids. Specific interaction energies and equilibrium intermolecular distances of asphaltenes and naphthenic acids are calculated using molecular mechanics. The results from molecular mechanics calculations support the experimental results of the titrations, and structure–property relationships are defined. Structure–property relationships are established for naphthenic acids, defining the relative contributions and importance of various functional groups: C═C, C═O, COOR, and COOH. The additive effects of naphthenic acids, defined by an increase in the precipitation onset, increase in the order of 5β-cholanic acid-3-one \u3c hydrogenated methyl abietate \u3c methyl abietate \u3c 5β-cholanic acid, with experiments containing 5β-cholanic acid-3-one containing unexpected and interesting results

Investigation of the Precipitation Behavior of Asphaltenes in the Presence of Naphthenic Acids Using Light Scattering and Molecular Modeling Techniques

A delay in the onset of flocculation is observed for asphaltenes in the presence of several naphthenic acids: methyl abietate, hydrogenated methyl abietate, 5β-cholanic acid, and 5β-cholanic acid-3-one. This flocculation behavior is monitored as a function of the added precipitant (<i>n</i>-heptane) to solutions of suspended asphaltenes and naphthenic acids in model solutions of toluene/<i>n</i>-heptane, using a combination of dynamic light scattering (DLS) and near-infrared (NIR) spectroscopic techniques. DLS and NIR show very good correlation in indentifying the onsets of flocculation, which varied among the series of naphthenic acids. Specific interaction energies and equilibrium intermolecular distances of asphaltenes and naphthenic acids are calculated using molecular mechanics. The results from molecular mechanics calculations support the experimental results of the titrations, and structure–property relationships are defined. Structure–property relationships are established for naphthenic acids, defining the relative contributions and importance of various functional groups: CC, CO, COOR, and COOH. The additive effects of naphthenic acids, defined by an increase in the precipitation onset, increase in the order of 5β-cholanic acid-3-one < hydrogenated methyl abietate < methyl abietate < 5β-cholanic acid, with experiments containing 5β-cholanic acid-3-one containing unexpected and interesting results