Theoretical transition frequencies beyond 0.1 ppb accuracy in H2+_2^+, HD+^+, and antiprotonic helium

We present improved theoretical calculations of transition frequencies for the fundamental transitions $(L\!=\!0,v\!=\!1)\to(L'\!=\!0,v'\!=\!0)$ in the hydrogen molecular ions H$_2^+$ and HD$^+$ with a relative uncertainty $4\cdot10^{-11}$ and for the two-photon transitions in the antiprotonic helium atom with a relative uncertainty $10^{-10}$. To do that, the one-loop self-energy correction of order $\alpha(Z\alpha)^6$ is derived in the two Coulomb center approximation, and numerically evaluated in the case of the aforementioned transitions. The final results also include a complete set of other spin-independent corrections of order $m\alpha^7$. The leading order corrections of $\alpha^2\ln^3(Z\alpha)^{-2}(Z\alpha)^6$ are also considered that allows to estimate a magnitude of yet uncalculated contributions.Comment: 10 pages, 2 figure, to be submitted to PR

One-loop vacuum polarization at mα7m\alpha^7 order for the two center problem

We present calculations of the one-loop vacuum polarization contribution (Uehling potential) for the two-center problem in the NRQED formalism. The cases of hydrogen molecular ions ($Z_1=Z_2=1$) as well as antiprotonic helium ($Z_1=2$, $Z_2=-1$) are considered. Numerical results of the vacuum polarization contribution at $m\alpha^7$ order for the fundamental transitions $(v=0,L=0)\to(v'=1,L'=0)$ in H$_2^+$ and HD$^+$ are presented.Comment: 6 pages, 2 figues, submitted to PR

Hydrogen molecular ions for improved determination of fundamental constants

The possible use of high-resolution rovibrational spectroscopy of the hydrogen molecular ions H + 2 and HD + for an independent determination of several fundamental constants is analyzed. While these molecules had been proposed for metrology of nuclear-to-electron mass ratios, we show that they are also sensitive to the radii of the proton and deuteron and to the Rydberg constant at the level of the current discrepancies colloquially known as the proton size puzzle. The required level of accuracy, in the 10 --12 range, can be reached both by experiments, using Doppler-free two-photon spectroscopy schemes, and by theoretical predictions. It is shown how the measurement of several well-chosen rovibrational transitions may shed new light on the proton-radius puzzle, provide an alternative accurate determination of the Rydberg constant, and yield new values of the proton-to-electron and deuteron-to-proton mass ratios with one order of magnitude higher precision

Biophysics Research Support at NASA/MSFC

No abstract availabl

High accuracy results for the energy levels of the molecular ions H2+, D2+ and HD+, up to J=2

We present a nonrelativistic calculation of the rotation-vibration levels of the molecular ions H2+, D2+ and HD+, relying on the diagonalization of the exact three-body Hamiltonian. The J=2 levels are obtained with a very high accuracy of 10^{-14} a.u. (for most levels) representing an improvement by five orders of magnitude over previous calculations. The accuracy is also improved for the J=1 levels of H2+ and D2+ with respect to earlier works. Moreover, we have computed the sensitivities of the energy levels with respect to the mass ratios, allowing these levels to be used for metrological purposes.Comment: 11 page

Sample selection and testing of separation processes

Phase partitioning, which has become an important tool for the separation and purification of biological materials, was studied. Instruments available for this technique were researched and a countercurrent distribution apparatus, the Biosheff MK2N, was purchased. Various proteins, polysaccharides and cells were studied as models to determine operating procedures and conditions for this piece of equipment. Results were compared with those obtained from other similar equipment, including a nonsynchronous coil planet centrifuge device. Additionally, work was done with affinity ligands attached to PEG, which can further enhance the separation capabilities of phase partitioning

Research reports: 1985 NASA/ASEE Summer Faculty Fellowship Program

A compilation of 40 technical reports on research conducted by participants in the 1985 NASA/ASEE Summer Faculty Fellowship Program at Marshall Space Flight Center (MSFC) is given. Weibull density functions, reliability analysis, directional solidification, space stations, jet stream, fracture mechanics, composite materials, orbital maneuvering vehicles, stellar winds and gamma ray bursts are among the topics discussed

Research Reports: 1984 NASA/ASEE Summer Faculty Fellowship Program

A NASA/ASEE Summer Faulty Fellowship Program was conducted at the Marshall Space Flight Center (MSFC). The basic objectives of the programs are: (1) to further the professional knowledge of qualified engineering and science faculty members; (2) to stimulate an exchange of ideas between participants and NASA; (3) to enrich and refresh the research and teaching activities of the participants' institutions; and (4) to contribute to the research objectives of the NASA Centers. The Faculty Fellows spent ten weeks at MSFC engaged in a research project compatible with their interests and background and worked in collaboration with a NASA/MSFC colleague. This document is a compilation of Fellows' reports on their research during the summer of 1984. Topics covered include: (1) data base management; (2) computational fluid dynamics; (3) space debris; (4) X-ray gratings; (5) atomic oxygen exposure; (6) protective coatings for SSME; (7) cryogenics; (8) thermal analysis measurements; (9) solar wind modelling; and (10) binary systems

Research Reports: 1983 NASA/ASEE Summer Faculty Fellowship Program

Thirty-five technical reports contain results of investigations in information and electronic systems; materials and processing; systems dynamics; structures and propulsion; and space sciences. Ecology at KSC, satellite de-spin, and the X-ray source monitor were also studied

Proton-electron mass ratio from HD+^+ revisited

We present a new derivation of the proton-electron mass ratio from the hydrogen molecular ion, HD$^+$. The derivation entails the adjustment of the mass ratio in highly precise theory so as to reproduce accurately measured ro-vibrational frequencies. This work is motivated by recent improvements of the theory, as well as the more accurate value of the electron mass in the recently published CODATA-14 set of fundamental constants, which justifies using it as input data in the adjustment, rather than the proton mass value as done in previous works. This leads to significantly different sensitivity coefficients and, consequently, a different value and larger uncertainty margin of the proton-electron mass ratio as obtained from HD$^+$