Academic literature on the topic 'Coupling Facility'

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Journal articles on the topic "Coupling Facility"

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Walker, Jonathan A., Jason D. Frieman, Mitchell L. R. Walker, Vadim Khayms, David King, and Peter Y. Peterson. "Electrical Facility Effects on Hall-Effect-Thruster Cathode Coupling: Discharge Oscillations and Facility Coupling." Journal of Propulsion and Power 32, no. 4 (July 2016): 844–55. http://dx.doi.org/10.2514/1.b35835.

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Matsui, Y., Y. Itahashi, M. Shimizu, and H. Tsuji. "Irradiation–coupling techniques using JMTR and another facility." Journal of Nuclear Materials 283-287 (December 2000): 997–1000. http://dx.doi.org/10.1016/s0022-3115(00)00347-0.

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Chang, Tieqiang, Yongkun Ding, Dongxian Lai, Tianxuan Huan, Shaoping Zhu, Zhijian Zheng, Guangyu Wang, et al. "Laser hohlraum coupling efficiency on the Shenguang II facility." Physics of Plasmas 9, no. 11 (November 2002): 4744–48. http://dx.doi.org/10.1063/1.1516781.

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Bailey, N. Y., C. Lusty, and P. S. Keogh. "Nonlinear flexure coupling elements for precision control of multibody systems." Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences 474, no. 2218 (October 2018): 20180395. http://dx.doi.org/10.1098/rspa.2018.0395.

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Conventional multibody systems used in robotics and automated machinery contain bearing components that exhibit complex and uncertain tribological characteristics. These limit fundamentally the precision of the automated motion and also cause wear. Replacing traditional bearing joints with flexure couplings eliminates these tribological effects, together with wear, reducing necessary system maintenance and offering a potential for increased motion precision. A flexure-coupled multibody system is considered and a novel general solution technique is presented. Derivation of a large deflection flexure coupling model is provided and subsequently validated using an experimental facility. A focused study of a unique double-flexure-coupling rigid body system is given; the formulated nonlinear mathematical model can be used for feedforward control. Equivalent control is also applied to a corresponding system with traditional bearing joints. The feasibility of replacing bearing joints by flexure couplings is demonstrated in terms of accurate large displacement control and reduction of high-frequency disturbances.
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Josten, J. W., C. Mohan, I. Narang, and J. Z. Teng. "DB2's use of the coupling facility for data sharing." IBM Systems Journal 36, no. 2 (1997): 327–51. http://dx.doi.org/10.1147/sj.362.0327.

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Sun, Lijun, Yue Zhao, Xia Wu, and Zengqiang Chen. "A comprehensive decoupling active disturbance rejection control for a gas flow facility." Transactions of the Institute of Measurement and Control 41, no. 2 (April 19, 2018): 297–310. http://dx.doi.org/10.1177/0142331218755578.

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Based on the linear active disturbance rejection control (LADRC), a comprehensive decoupling controller for gas flow facilities is presented to guarantee stability and a fast response during the process of gas flowmeter performance tests. First, a mathematical model is developed to describe the pressure-flow coupling system. Then, a step response method is applied to identify parameters of this model. To realize the effective decoupling control, the static coupling part is introduced into the LADRC design. The overall effect of the dynamic coupling part among two channels, the internal uncertainties and the external disturbance, are treated as total disturbance, which is estimated using the extended state observer and cancelled out by the control law. After estimating and cancelling, the pressure-flow coupling system can be transformed into two single input single output subsystems with the form of cascade integrators. Then two proportional differential controllers are applied to control the two simplified subsystems. Simulation and experimental results show that the proposed algorithm has a shorter settling time, a more effective decoupling effect and a greater capability of disturbance rejecting and stronger performance robustness in gas flow facility than conventional proportional–integral–derivative algorithms.
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Goncharov, Alexander F., Irina Chuvashova, Cheng Ji, and Ho-kwang Mao. "Intermolecular coupling and fluxional behavior of hydrogen in phase IV." Proceedings of the National Academy of Sciences 116, no. 51 (December 3, 2019): 25512–15. http://dx.doi.org/10.1073/pnas.1916385116.

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We performed Raman and infrared (IR) spectroscopy measurements of hydrogen at 295 K up to 280 GPa at an IR synchrotron facility of the Shanghai Synchrotron Radiation Facility (SSRF). To reach the highest pressure, hydrogen was loaded into toroidal diamond anvils with 30-μm central culet. The intermolecular coupling has been determined by concomitant measurements of the IR and Raman vibron modes. In phase IV, we find that the intermolecular coupling is much stronger in the graphenelike layer (G layer) of elongated molecules compared to the Br2-like layer (B layer) of shortened molecules and it increases with pressure much faster in the G layer compared to the B layer. These heterogeneous lattice dynamical properties are unique features of highly fluxional hydrogen phase IV.
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Orjuela-Castro, Javier Arturo, Lizeth Andrea Sanabria-Coronado, and Andrés Mauricio Peralta-Lozano. "Coupling facility location models in the supply chain of perishable fruits." Research in Transportation Business & Management 24 (September 2017): 73–80. http://dx.doi.org/10.1016/j.rtbm.2017.08.002.

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Surman, D. H. "The IBM z Systems Coupling Facility exploitation of storage-class memory." IBM Journal of Research and Development 59, no. 4/5 (July 2015): 8:1–8:9. http://dx.doi.org/10.1147/jrd.2015.2430052.

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Manes, K. R., O. C. Barr, E. S. Bliss, R. P. Drake, R. O. Godwin, D. G. Gritton, J. S. Hildum, et al. "Novette facility: activation and experimental results." Laser and Particle Beams 3, no. 2 (May 1985): 173–88. http://dx.doi.org/10.1017/s0263034600001373.

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From the neodymium glass laser system Novette with two beams of 74 cm diameter and 18 kJ energy per pulse output in the nanosecond range, the design, the steps of the construction, and results of the system are reported. The two beams are synchronized to 5 psec and conversion to green light up to 78% has been realized. Conversion to four times the laser frequency is measured with more than 25% conversion. Simulation and measurement of laser beam properties at several locations permit an analysis to define the final Nova configuration. About half of Novette's experiments were to study short wave length laser–plasma interactions for the then better coupling by inverse bremsstrahlung mechanisms for inertial confinement fusion with laser intensities up to 1017W/cm2. Experiments were divided between high density implosion research and non-local thermodynamic equilibrium plasma conditions.
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Dissertations / Theses on the topic "Coupling Facility"

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Cook, James Richard. "Development of an aeroelastic methodology for surface morphing rotors." Diss., Georgia Institute of Technology, 2014. http://hdl.handle.net/1853/51807.

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A Computational Fluid Dynamics/Computational Fluid Dynamics (CFD/CSD) coupling interface was developed to obtain aeroelastic solutions of a morphing rotor. The methodology was implemented in Fully Unstructured Navier-Stokes (FUN3D) solver, which communicates aerodynamic forces on the blade surface to University of Michigan’s Nonlinear Active Beam Solver (UM/NLABS) and then imports structural deflections of the blade surface during each time step. Development of this methodology adds the capability to model elastic rotors with flexible airfoils. The method was validated through an aerodynamic work analysis, comparison of sectional blade loads and deflections with experimental data, and two-dimensional stability analyses for pitch/plunge flutter and camber flutter. Computational simulations were performed for a rotor in forward flight with the CFD/CSD solver and with a comprehensive CSD solver using finite-state (F-S) aerodynamics, and results were compared. Prescribed three-per-revolution camber deflections were then applied, and solutions of the CFD/CSD and comprehensive CSD computations indicated that three-per-revolution camber actuation has the potential to minimize hub forces and moments with deflections as small as 0.25%c. In anticipation of active rotor experiments inside enclosed facilities, the capability of CFD for accurately simulating flow inside enclosed volumes was examined. It was determined that URANS models are not suitable for rotor simulations in an enclosed facility, and components that are a distance of two to three rotor radii from the hub were also observed to have a large influence on recirculation and performance.
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Spruth, Wilhelm G. "Enterprise Computing." Universitätsbibliothek Leipzig, 2013. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-126859.

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Das vorliegende Buch entstand aus einer zweisemestrigen Vorlesung „Enterprise Computing“, die wir gemeinsam über viele Jahre als Teil des Bachelor- oder Master-Studienganges an der Universität Leipzig gehalten haben. Das Buch führt ein in die Welt des Mainframe und soll dem Leser einen einführenden Überblick geben. Band 1 ist der Einführung in z/OS gewidmet, während sich Band 2 mit der Internet Integration beschäftigt. Ergänzend werden in Band 3 praktische Übungen unter z/OS dargestellt.
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Books on the topic "Coupling Facility"

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Day, Richard E. Coupling dynamics in aircraft: A historical perspective. [Washington, D.C.]: National Aeronautics and Space Administration, Office of Management, Scientific and Technical Information Program, 1997.

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Baddeley, Ryan J. Development of an experimental facility for studying mass and energy coupling in a two-phase free shear flow. 1994.

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Book chapters on the topic "Coupling Facility"

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Jore, Sissel H. "Security and Safety Culture—Dual or Distinct Phenomena?" In The Coupling of Safety and Security, 43–51. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-47229-0_5.

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Abstract The commission that investigated the terrorist attacks against the Algerian oil facility In Amenas concluded that the Norwegian petroleum company Statoil should establish a security culture distinct from its safety culture. Both are elements of organizational culture, so how should organizations relate to this new concept of security culture? This chapter explores the adequacy of the concept of security culture and explores whether these phenomena should be considered as a duality or separately. The adequacy of security culture is discussed in terms of how the concept is used in the In Amenas investigation report. Despite the lack of demarcation and operationalization of the security culture concept, we conclude, there is a need to further develop security culture as a theoretical and practical element. Security and safety culture should be understood separately, but in practical reality should not be treated as distinct.
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Kruer, William L. "Laser-Plasma Coupling with Ignition-Scale Targets: New Regimes and Frontiers on the National Ignition Facility." In Laser-Plasma Interactions and Applications, 221–42. Heidelberg: Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-00038-1_9.

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Bérest, P., B. Brouard, P. de Laguérie, T. You, D. Fourmaintraux, and J. Héas. "A salt-cavern abandonment test in an LPG storage facility." In Eurock 2006: Multiphysics Coupling and Long Term Behaviour in Rock Mechanics, 455–60. Taylor & Francis, 2006. http://dx.doi.org/10.1201/9781439833469.ch65.

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Chen, W., G. Wu, J. Yang, and C. Yang. "The feasibility analysis of abandoned salt caverns for underground gas storage facility." In Eurock 2006: Multiphysics Coupling and Long Term Behaviour in Rock Mechanics, 367–72. Taylor & Francis, 2006. http://dx.doi.org/10.1201/9781439833469.ch52.

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Taber, Douglass F. "The Nicolaou Synthesis of (+)-Hirsutellone B." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0089.

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(+)-Hirsutellone B 3, isolated from the insect pathogenic fungus Hirsutella nivea BCC 2594, shows good activity (MIC = 0.78 μg/mL) against Mycobacterium tuberculosis. Approaching the synthesis of 3, K. C. Nicolaou of Scripps/La Jolla envisioned and reduced to practice (Angew. Chem. Int. Ed. 2009, 49, 6870) a spectacular tandem intramolecular epoxide opening: internal Diels-Alder cyclization (1 2) that established all three of the carbocyclic rings of 3 with the proper relative and absolute configuration. The construction of 1 began with commercial ( R) -(+)-citronellal 4. Wittig homologation established the ( Z )-iodide 5. Selective ozonolysis followed by condensation with the phosphorane 7 set the stage for Jørgensen-Córdova (Tetrahedron Lett. 2006, 47, 99) epoxidation with H2O2 and a catalytic amount of the Hayashi catalyst 9. Condensation of 10 with the phosphorane 11 followed by Cu-catalyzed coupling of 12 with the organostannane 13 completed the assembly of 1. This approach underscores the strategic advantages of the Jørgensen-Córdova epoxidation over the Sharpless protocol. It is not necessary to reduce the aldehyde to the allyic alcohol, then reoxidize. Furthermore, the Jørgensen-Córdova epoxidation, using catalytic 9, is operationally easier than the Sharpless procedure, which often uses stoichiometric amounts of tartrate ester. The cyclization of 1 proceeded by way of 13, with the newly formed stereogenic center having the diene equatorial on the cyclohexane. Endo cycloaddition catalyzed by the Lewis acid in the solution then gave 2. The facility with which the cyclization of 13 set both the substituents and the stereogenic centers of 2 raises the possibility that the biosynthesis might also follow such an internal [4 + 2] cycloaddition. To complete the synthesis of 3, it was necessary to construct the strained paracyclophane. The authors took advantage of the facile cyclization of the thiolate liberated from 18, then installed the ring-contracted alkene with a Ramburg-Bäcklund rearrangement of 19. They completed the synthesis of (+)-hirsutellone B 3 by exposing the ketone 21 to NH3 in CH3OH/H2O.
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Taber, Douglass. "The Castle Synthesis of (-)-Acutumine." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0104.

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The complex tetracyclic alkaloid (-)-acutumine 3, isolated from the Asian vine Menispermum dauricum, shows selective T-cell toxicity. The two adjacent cyclic all-carbon quaternary centers of 3 offered a particular challenge. Steven L. Castle of Brigham Young University solved (J. Am. Chem. Soc. 2009, 131, 6674) this problem by effecting net enantioselective conjugate allylation of the enantiomerically pure substrate 1 to give 2 with high diastereocontrol. The starting coupling partners ( Organic Lett . 2006, 8, 3757; Organic Lett. 2007, 9, 4033) for the synthesis were the Weinreb amide 4, prepared over several steps from 2,3- dimethoxyphenol, and the diastereomerically- and enantiomerically-pure cyclopentenyl iodide 5, prepared by singlet oxygenation of cyclopentadiene followed by enzymatic hydrolysis. Transmetalation of 5 by the Knochel protocol, addition of the resulting organometallic to 4 and enantioselective (and therefore diastereoselective) reduction of the resulting ketone delivered the alcohol 6. Methods for installing cyclic halogenated stereogenic centers are not well developed. Exposure of the allylic alcohol to mesyl chloride gave the chloride 7 with inversion of absolute configuration. Remarkably, this chlorinated center was carried through the rest of the synthesis without being disturbed. A central step in the synthesis of 3 was the spirocyclization of 7 to 8. Initially, iodine atom abstraction generated the aryl radical. The diastereoselectivity of the radical addition to the cyclopentene was set by the adjacent silyloxy group. The α-keto radical so generated reacted with the Et3Al to give a species that was oxidized by the oxaziridine to the α-keto alcohol, again with remarkable diastereocontrol. Conjugate addition to the cyclohexenone 1 failed, so an alternative strategy was developed, diastereoselective 1,2-allylation of the ketone followed by oxy-Cope rearrangement. The stereogenic centers of 1 are remote from the cyclohexenone carbonyl, so could not be used to control the facial selectivity of the addition. Fortunately, the stoichiometric enantiomerically-pure Nakamura reagent delivered the allyl group preferentially to one face of the ketone 1, to give 9. The subsequent sigmatropic rearrangement to establish the very congested second quaternary center of 2 then proceeded with remarkable facility, at 0°C for one hour.
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Taber, Douglass F. "The Magnus Synthesis of ( ± )-Codeine." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0088.

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Although there have been many synthetic approaches to morphine and its methyl ether codeine 3, the pentacyclic structure of these Papaver alkaloids continues to intrigue organic chemists. Philip Magnus of the University of Texas devised (J. Am. Chem. Soc . 2009, 131, 16045) an elegant route to 3 based on the conversion of 1 to 2 by way of an intramolecular Michael addition. The starting point for the synthesis was the commercial bromoaldehyde 4. Coupling with 5 delivered the substituted biphenyl 6, which was carried on to the mixed bromo acetal 8. On exposure to fluoride ion, 8 was desilylated, and the intermediate phenoxide cyclized with impressive facility to give 1. Exposure of 1 to nitromethane delivered the tetracyclic 2. This reaction apparently was initiated by Henry addition of the nitromethane to the aldehyde. The intramolecular Michael addition of the intermediate Henry adduct then proceeded to give the desired cis diastereomer of the newly formed ring. Finally, loss of water gave 2. Conjugate reduction of the nitroalkene 2 led to 9 with remarkable diastereocontrol. Exposure of 9 to LiAlH4 converted the nitro group to the amine and the enone to the allylic alcohol. On exposure to acid, the hemiacetal was hydrolyzed. The liberated aldehyde underwent reductive amination with the free amine, while at the same time ionic cyclization closed the ether ring. N-acylation completed the conversion to 10. The ether 10 had previously been converted to codeine and then, in a single demethylation step, to morphine. In that synthesis, the alkene of 10 was directly epoxidized. The resulting “up” epoxide reacted only sluggishly with phenylselenide anion, and the relative configuration of the resulting allylic alcohol had to be inverted by oxidation followed by reduction. In the current synthesis, exposure of the alkene 10 to dibromohydantoin under aqueous conditions to form the bromohydrin effected concomitant arene bromination, to give, after base treatment, the “down” epoxide 12. Phenylselenide opening of the epoxide was then facile, and the product allylic alcohol had the correct relative configuration for codeine and morphine. The extra Br was of no consequence, as it was removed by the final LiAlH4 reduction.
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Conference papers on the topic "Coupling Facility"

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Sheeley, Joseph, D. Sells, R. Bates, and L. Bates. "Experiences with Coupling Facility Control Systems with Control Volume Facility Models." In 42nd AIAA Aerospace Sciences Meeting and Exhibit. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2004. http://dx.doi.org/10.2514/6.2004-932.

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Beham, Andreas, Monika Kofler, Stefan Wagner, and Michael Affenzeller. "Coupling simulation with HeuristicLab to solve facility layout problems." In 2009 Winter Simulation Conference - (WSC 2009). IEEE, 2009. http://dx.doi.org/10.1109/wsc.2009.5429238.

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Song, Danrong, Tong Liu, and Hua Zhao. "Economic Evaluation of Nuclear Reactor Coupling with Seawater Desalination Facility." In 14th International Conference on Nuclear Engineering. ASMEDC, 2006. http://dx.doi.org/10.1115/icone14-89171.

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Nowadays only 1/2000 of overall fresh water resource can be used in the world, 1.1 billion people in the world are short of safety drinkable water, so the supply of freshwater is one of the major problems facing to the world in 21st century. China is one of the thirteen water-poorest countries and fresh water has become a choke point of the economic development in those water-poor regions. The desalination of sea water is a very important way to find new fresh water resource and sea water is inexhaustible.
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Leibowicz, B., C. Thompson, K. Clarno, and C. Bourque. "Coupling Simulation Technologies to Assist Nuclear Fuel Fabrication Facility Design." In 2020 ANS Virtual Winter Meeting. AMNS, 2020. http://dx.doi.org/10.13182/t123-33395.

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Cheng, Ning-Bo, Bin Feng, Fu-Quan Li, Huai-Ting Jia, Yong Xiang, and Xiao-Feng Wei. "A target positioning method for ICF laser facility without translational kinematic coupling." In XX International Symposium on High Power Laser Systems and Applications, edited by Chun Tang, Shu Chen, and Xiaolin Tang. SPIE, 2015. http://dx.doi.org/10.1117/12.2065306.

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Ghorayeb, Kassem, Jonathan Holmes, Richard Torrens, and Balraj Grewal. "A General Purpose Controller for Coupling Multiple Reservoir Simulations and Surface Facility Networks." In SPE Reservoir Simulation Symposium. Society of Petroleum Engineers, 2003. http://dx.doi.org/10.2118/79702-ms.

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Furuya, M., T. Fukahori, S. Mizokami, and J. Yokoya. "DEVELOPMENT OF BWR REGIONAL STABILITY FACILITY SIRIUS-F, WHICH SIMULATES THERMALHYDRAULICS-NEUTRONICS COUPLING." In Annals of the Assembly for International Heat Transfer Conference 13. Begell House Inc., 2006. http://dx.doi.org/10.1615/ihtc13.p24.140.

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Antoneus, Sarjono Tasi, Feroney Serbini, Ammar Mohamad Azili, Muhammad Firdaus Hassan, Raja Zuhaili Aimran Raja Zainal Raffik, M. Azri Aizat Tugimin, Wei Shen Ong, and Ba Loi Trinh. "Unlocking Surface Constraints through Integrated Operation : A Production Network-to-Process Facility Coupling Method." In SPE/IATMI Asia Pacific Oil & Gas Conference and Exhibition. Society of Petroleum Engineers, 2019. http://dx.doi.org/10.2118/196235-ms.

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Schneider, M. B., D. E. Hinkel, D. E. Bower, H. C. Bruns, K. M. Campbell, J. R. Celeste, S. Compton, et al. "Coupling of High Power Lasers to Small, Hot Targets at the National Ignition Facility." In IEEE Conference Record - Abstracts. 2005 IEEE International Conference on Plasma Science. IEEE, 2005. http://dx.doi.org/10.1109/plasma.2005.359136.

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Wu, X., H. Blosser, D. Johnson, F. Marti, and R. C. York. "The K500-to-K1200 coupling line for the coupled cyclotron facility at the NSCL." In Proceedings of the 1999 Particle Accelerator Conference (Cat. No.99CH36366). IEEE, 1999. http://dx.doi.org/10.1109/pac.1999.795534.

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Reports on the topic "Coupling Facility"

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Fournier, K., C. Brown, M. May, W. Dunlop, S. Compton, J. Kane, P. Mirkarimi, R. Guyton, and E. Huffman. ENERGY PARTITIONING, ENERGY COUPLING (EPEC) EXPERIMENTS AT THE NATIONAL IGNITION FACILITY. Office of Scientific and Technical Information (OSTI), January 2012. http://dx.doi.org/10.2172/1034490.

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