122 research outputs found

    On thermo-mechanical fatigue in single crystal Ni-base superalloys

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    AbstractThermo-mechanical fatigue (TMF) is a critical damage process in gas turbine jet engines. Reliable life prediction methodologies are required both for design and life management. Current life estimation approaches are computationally burdensome and/or semi-empirical, significantly limiting their application. Complexity comes about from the multiplicity of damage processes which occur during the simultaneously changing temperatures and loads, characteristic of TMF. Furthermore, these processes interact in ways that are not observed for isothermal LCF. These interactions usually accelerate damage processes and result in significantly reduced TMF life, when compared to other fatigue scenarios. The results of a multiphased approach to life prediction will be presented. In phase I the Neu-Sehitoglu (N-S) cumulative damage model was used to: a) provide initial life predictions and b) identify processes and interactions which most significantly control the life under TMF loading. The N-S model is based on a linear damage summation rule which both explicitly and implicitly includes damage interactions. In phase II a sensitivity analysis incorporating statistical concepts was performed on the N-S model parameters. Specifically a nonlinear optimization was performed to determine optimal parameter values in order to maximize agreement with experimental results (well within 2X). In phase III, informed by phases I and II, a physics-based fatigue/oxidation (also recognizing creep effects) model was developed which correctly predicts effects of frequency, hold-time, temperature, and strain range and oxidation kinetics

    Rover Low Gain Antenna Qualification for Deep Space Thermal Environments

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    A method to qualify the Rover Low Gain Antenna (RLGA) for use during the Mars Science Laboratory (MSL) mission has been devised. The RLGA antenna must survive all ground operations, plus the nominal 670 Martian sol mission that includes the summer and winter seasons of the Mars thermal environment. This qualification effort was performed to verify that the RLGA design, its bonding, and packaging processes are adequate. The qualification test was designed to demonstrate a survival life of three times more than all expected ground testing, plus a nominal 670 Martian sol missions. Baseline RF tests and a visual inspection were performed on the RLGA hardware before the start of the qualification test. Functional intermittent RF tests were performed during thermal chamber breaks over the course of the complete qualification test. For the return loss measurements, the RLGA antenna was moved to a test area. A vector network analyzer was calibrated over the operational frequency range of the antenna. For the RLGA, a simple return loss measurement was performed. A total of 2,010 (3 670 or 3 times mission thermal cycles) thermal cycles was performed. Visual inspection of the RLGA hardware did not show any anomalies due to the thermal cycling. The return loss measurement results of the RLGA antenna after the PQV (Package Qualification and Verification) test did not show any anomalies. The antenna pattern data taken before and after the PQV test at the uplink and downlink frequencies were unchanged. Therefore, the developed design of RLGA is qualified for a long-duration MSL mission

    The hydrogen effects on materials program at NIST-Boulder

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    Novel Naphthalene-Based Inhibitors of Trypanosoma brucei RNA Editing Ligase 1

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    African sleeping sickness is a devastating disease that plagues sub-Saharan Africa. Neglected tropical diseases like African sleeping sickness cause significant death and suffering in the world's poorest countries. Current treatments for African sleeping sickness either have high costs, terrible side effects, or limited effectiveness. Consequently, new medicines are urgently needed. RNA editing ligase 1 is an important protein critical for the survival of Trypanosoma brucei, the unicellular parasite that causes African sleeping sickness. In this paper, we describe our recent efforts to use advanced computer techniques to identify chemicals predicted to prevent RNA editing ligase 1 from functioning properly. We subsequently tested our predicted chemicals and confirmed that a number of them inhibited the protein's function. Additionally, one of the chemicals was effective at stopping the growth of the parasite in culture. Although substantial work remains to be done in order to optimize these chemicals so they are effective and safe to use in human patients, the identification of these parasite-killing compounds is nevertheless a valuable step towards finding a better cure for this devastating disease

    Modeling the pharmacodynamics of passive membrane permeability

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    Small molecule permeability through cellular membranes is critical to a better understanding of pharmacodynamics and the drug discovery endeavor. Such permeability may be estimated as a function of the free energy change of barrier crossing by invoking the barrier domain model, which posits that permeation is limited by passage through a single “barrier domain” and assumes diffusivity differences among compounds of similar structure are negligible. Inspired by the work of Rezai and co-workers (JACS 128:14073–14080, 2006), we estimate this free energy change as the difference in implicit solvation free energies in chloroform and water, but extend their model to include solute conformational affects. Using a set of eleven structurally diverse FDA approved compounds and a set of thirteen congeneric molecules, we show that the solvation free energies are dominated by the global minima, which allows solute conformational distributions to be effectively neglected. For the set of tested compounds, the best correlation with experiment is obtained when the implicit chloroform global minimum is used to evaluate the solvation free energy difference

    Policy Recommendations for Meeting the Grand Challenge to Achieve Equal Opportunity and Justice

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    This brief was created forSocial Innovation for America’s Renewal, a policy conference organized by the Center for Social Development in collaboration with the American Academy of Social Work & Social Welfare, which is leading theGrand Challenges for Social Work initiative to champion social progress. The conference site includes links to speeches, presentations, and a full list of the policy briefs
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