1,548 research outputs found

    Experimental investigation on the influencing factors of a transcritical CO2 heat pump

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    The concept of “the optimal heat rejection pressure” has attracted wide attention in refrigeration community. Unlike the conventional refrigerants, the heat rejection pressure and temperature of the gas-cooler in the transcritical CO2 cycle are usually decoupled in the transcritical cycle. Besides, there exists an optimal heat rejection pressure under which the maximum cycle efficiency can be achieved. Therefore, the interaction effect between heat rejection pressure and system performance has been studied by many researchers. The heat rejection pressure of the gas-cooler has great impact on the COP of the transcritical CO2 system, but the investigation on the influence factors of the heat rejection pressure is quite rare in open literature. In this paper, the effects of the water inlet temperatures and the water flow rates on the heat rejection pressure of a water-to-water transcritical CO2 refrigeration heat pump with single-stage expansion system have been investigated. Furthermore, the operation parameters and the performance of the system are also evaluated

    Cosmic star formation rate density from DLAs and the HI-metallicity relation

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    Design and Setup of the Micro-Turboexpander Transcritical CO2 System

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    As the potential Eco-friendly refrigerant, CO2 regains more and more attentions. It has various advantages over conventional refrigerants, such as non-flammability, non-toxicity, high volumetric refrigerant capacity and excellent heat transfer properties. Because the heat rejection temperature in a transcritical CO2 heat pump or a transcritical CO2 refrigeration system is higher than the critical temperature of CO2, the transcritical vapor compression cycle becomes the best choice for transcritical CO2 systems. However, the relative low COP caused by the throttle valve limited the further development. The replacement of a throttle valve with a turboexpander, an ejector or a vortex tube is leading to the way for improving the COP of a transcritical CO2 system. With the advantages of high efficiency, high compactness, high reliability and long-life time, turboexpanders have been widely used in gas lique faction devices (below 120K) and most of the reverse Brayton refrigeration systems. It is also one of the most ideal expansion devices for transcritical CO2 systems. However, its applications are limited by the difficulties of high pressure and super high rotating speed operation. With the development of manufacturing technology and gas bearing technology, it becomes possible to use turboexpanders in transcriticalCO2 systems. In this paper, two turboexpanders with 10 mm radial reaction turbine wheel and 9 mm rotor diameter were designed for the 15 kW transcritical CO2 refrigeration system, and the rotating speed is about 200 krpm.The proposed turboexpanders outlet states are CO2 two-phase flow and subcooled CO2 liquid flow, respectively. This study will lay a foundation for the application of turboexpanders in transcritical CO2 systems

    spl(2,1) dynamical supersymmetry and suppression of ferromagnetism in flat band double-exchange models

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    The low energy spectrum of the ferromagnetic Kondo lattice model on a N-site complete graph extended with on-site repulsion is obtained from the underlying spl(2,1) algebra properties in the strong coupling limit. The ferromagnetic ground state is realized for 1 and N+1 electrons only. We identify the large density of states to be responsible for the suppression of the ferromagnetic state and argue that a similar situation is encountered in the Kagome, pyrochlore, and other lattices with flat bands in their one-particle density of states.Comment: 7 pages, 1 figur

    Investigation of bonded hydrogen defects in nanocrystalline diamond films grown with nitrogen/methane/hydrogen plasma at high power conditions

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    In this work, we investigate the influence of some growth parameters such as high microwave power ranging from 3.0 to 4.0 kW and N2 additive on the incorporation of bonded hydrogen defects in nanocrystalline diamond (NCD) films grown through a small amount of pure N2 addition into conventional 4% CH4/H2 plasma using a 5 kW microwave plasma CVD system. Incorporation form and content of hydrogen point defects in the NCD films produced with pure N2 addition was analyzed by employing Fourier-transform infrared (FTIR) spectroscopy for the first time. A large amount of hydrogen related defects was detected in all the produced NCD films with N2 additive ranging from 29 to 87 µm thick with grain size from 47 nm to 31 nm. Furthermore, a specific new H related sharp absorption peak appears in all the NCD films grown with pure N2/CH4/H2 plasma at high powers and becomes stronger at powers higher than 3.0 kW and is even stronger than the 2920 cm−1 peak, which is commonly found in CVD diamond films. Based on these experimental findings, the role of high power and pure nitrogen addition on the growth of NCD films including hydrogen defect formation is analyzed and discussed

    BDsπB \to D_s \pi and the tree amplitude in Bπ+πB \to \pi^+ \pi^-

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    The recently-observed decay B0Ds+πB^0 \to D_s^+ \pi^- is expected to proceed mainly by means of a tree amplitude in the factorization limit: B0π(W+)B^0 \to \pi^- {(W^+)}^*, (W+)Ds+{(W^+)}^* \to D_s^+. Under this assumption, we predict the corresponding contribution of the tree amplitude to B0π+πB^0 \to \pi^+ \pi^-. We indicate the needed improvements in data that will allow a useful estimate of this amplitude with errors comparable to those accompanying other methods. Since the factorization hypothesis for this process goes beyond that proved in most approaches, we also discuss independent tests of this hypothesis.Comment: 7 pages, LaTeX, 1 figure, to be submitted to Phys. Rev. D (Brief Reports

    Fast determination of thiacloprid by photoinduced chemiluminescence

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    This paper was published in Applied Spectroscopy and is made available as an electronic reprint with the permission of OSA. The paper can be found at the following URL on the OSA website: http://www.opticsinfobase.org/as/abstract.cfm?URI=as-68-6-642. Systematic or multiple reproduction or distribution to multiple locations via electronic or other means is prohibited and is subject to penalties under law.A new and sensitive application of the chemiluminescence detection has been developed for the determination of the pesticide thiacloprid in water. It was based on the on-line photoreaction of thiacloprid in basic medium, with quinine acting as sensitizer of the chemiluminescent response; Cerium (IV) in sulfuric acid medium was used as oxidant. A high automation and reproducibility was provided by a flow injection analysis (FIA) manifold. The validation of the method was performed in terms of selectivity, linearity, LOD, precision and accuracy. Liquid chromatography with UV detection was used as reference for mineral, tap, ground and spring water samples. The proposed method is fast (throughput of 130 h-1), sensitive (LOD of 0.8 ng mL-1 without preconcentration steps and 0.08 ng mL-1 with solid phase extraction (SPE)), low-cost and possible to couple with separative methods for the simultaneous determination of other pesticides. The enhanced chemiluminescence intensity was linear with thiacloprid concentration over the (2-80) and (80-800) ng mL-1 ranges. A possible reaction mechanism is also discussed.The authors thank the Ministerio de Educacion y Ciencia of Spain and the Fondo Europeo de Desarrollo Regional for financial support, Project CTM2006-11991.Catalá Icardo, M.; López Paz, JL.; Pérez Plancha, LM. (2014). Fast determination of thiacloprid by photoinduced chemiluminescence. Applied Spectroscopy. 68(6):642-648. https://doi.org/10.1366/13-07330S642648686Tomizawa, M., & Casida, J. E. (2005). NEONICOTINOID INSECTICIDE TOXICOLOGY: Mechanisms of Selective Action. Annual Review of Pharmacology and Toxicology, 45(1), 247-268. doi:10.1146/annurev.pharmtox.45.120403.095930Tapparo, A., Giorio, C., Soldà, L., Bogialli, S., Marton, D., Marzaro, M., & Girolami, V. (2012). UHPLC-DAD method for the determination of neonicotinoid insecticides in single bees and its relevance in honeybee colony loss investigations. Analytical and Bioanalytical Chemistry, 405(2-3), 1007-1014. doi:10.1007/s00216-012-6338-3Tennekes, H. A., & Sánchez-Bayo, F. (2013). The molecular basis of simple relationships between exposure concentration and toxic effects with time. Toxicology, 309, 39-51. doi:10.1016/j.tox.2013.04.007Peña, A., Rodríguez-Liébana, J. A., & Mingorance, M. D. (2011). Persistence of two neonicotinoid insecticides in wastewater, and in aqueous solutions of surfactants and dissolved organic matter. Chemosphere, 84(4), 464-470. doi:10.1016/j.chemosphere.2011.03.039Di Muccio, A., Fidente, P., Barbini, D. A., Dommarco, R., Seccia, S., & Morrica, P. (2006). Application of solid-phase extraction and liquid chromatography–mass spectrometry to the determination of neonicotinoid pesticide residues in fruit and vegetables. Journal of Chromatography A, 1108(1), 1-6. doi:10.1016/j.chroma.2005.12.111Fidente, P., Seccia, S., Vanni, F., & Morrica, P. (2005). Analysis of nicotinoid insecticides residues in honey by solid matrix partition clean-up and liquid chromatography–electrospray mass spectrometry. Journal of Chromatography A, 1094(1-2), 175-178. doi:10.1016/j.chroma.2005.09.012Seccia, S., Fidente, P., Barbini, D. A., & Morrica, P. (2005). Multiresidue determination of nicotinoid insecticide residues in drinking water by liquid chromatography with electrospray ionization mass spectrometry. Analytica Chimica Acta, 553(1-2), 21-26. doi:10.1016/j.aca.2005.08.006Pareja, L., Martínez-Bueno, M. J., Cesio, V., Heinzen, H., & Fernández-Alba, A. R. (2011). Trace analysis of pesticides in paddy field water by direct injection using liquid chromatography–quadrupole-linear ion trap-mass spectrometry. Journal of Chromatography A, 1218(30), 4790-4798. doi:10.1016/j.chroma.2011.02.044Seccia, S., Fidente, P., Montesano, D., & Morrica, P. (2008). Determination of neonicotinoid insecticides residues in bovine milk samples by solid-phase extraction clean-up and liquid chromatography with diode-array detection. Journal of Chromatography A, 1214(1-2), 115-120. doi:10.1016/j.chroma.2008.10.088Wang, W., Li, Y., Wu, Q., Wang, C., Zang, X., & Wang, Z. (2012). Extraction of neonicotinoid insecticides from environmental water samples with magnetic graphene nanoparticles as adsorbent followed by determination with HPLC. Analytical Methods, 4(3), 766. doi:10.1039/c2ay05734dBi, X., & Yang, K.-L. (2009). On-Line Monitoring Imidacloprid and Thiacloprid in Celery Juice Using Quartz Crystal Microbalance. Analytical Chemistry, 81(2), 527-532. doi:10.1021/ac801786aGámiz-Gracia, L., Garcı́a-Campaña, A. M., Soto-Chinchilla, J. J., Huertas-Pérez, J. F., & González-Casado, A. (2005). Analysis of pesticides by chemiluminescence detection in the liquid phase. TrAC Trends in Analytical Chemistry, 24(11), 927-942. doi:10.1016/j.trac.2005.05.009Roda, A., & Guardigli, M. (2011). Analytical chemiluminescence and bioluminescence: latest achievements and new horizons. Analytical and Bioanalytical Chemistry, 402(1), 69-76. doi:10.1007/s00216-011-5455-8Du, J., & Li, H. (2010). Sensitive Chemiluminescence Determination of Thirteen Cephalosporin Antibiotics with Luminol—Copper(II) Reaction. Applied Spectroscopy, 64(10), 1154-1159. doi:10.1366/000370210792973613Li, Y., Li, Y., & Yang, Y. (2011). Flow-Injection Chemiluminescence Determination of Lisinopril Using Luminol–KMnO4 Reaction Catalyzed by Silver Nanoparticles. Applied Spectroscopy, 65(4), 376-381. doi:10.1366/10-06115Catalá-Icardo, M., López-Paz, J. L., Choves-Barón, C., & Peña-Bádena, A. (2012). Native vs photoinduced chemiluminescence in dimethoate determination. Analytica Chimica Acta, 710, 81-87. doi:10.1016/j.aca.2011.10.043Mestre, Y. F., Zamora, L. L., & Calatayud, J. M. (2001). Flow-chemiluminescence: a growing modality of pharmaceutical analysis. Luminescence, 16(3), 213-235. doi:10.1002/bio.608Lara, F. J., García-Campaña, A. M., & Aaron, J.-J. (2010). Analytical applications of photoinduced chemiluminescence in flow systems—A review. Analytica Chimica Acta, 679(1-2), 17-30. doi:10.1016/j.aca.2010.09.001Icardo, M. C., & Calatayud, J. M. (2008). Photo-Induced Luminescence. Critical Reviews in Analytical Chemistry, 38(2), 118-130. doi:10.1080/10408340802039609RICART, I., ANTONFOS, G., DUART, M., MATEO, J., ZAMORA, L., & CALATAYUD, J. (2007). Theoretical prediction of the photoinduced chemiluminescence of pesticides. Talanta, 72(2), 378-386. doi:10.1016/j.talanta.2006.10.048Abramović, B. F., Banić, N. D., & Šojić, D. V. (2010). Degradation of thiacloprid in aqueous solution by UV and UV/H2O2 treatments. Chemosphere, 81(1), 114-119. doi:10.1016/j.chemosphere.2010.07.016Icardo, M. (2003). FI-on line photochemical reaction for direct chemiluminescence determination of photodegradated chloramphenicol. Talanta, 60(2-3), 405-414. doi:10.1016/s0039-9140(03)00074-2Zhao, Y., Baeyens, W. R. G., Zhang, X., Calokerinos, A. C., Nakashima, K., & Der Weken, G. V. (1997). Chemiluminescence Determination of Tiopronin by Flow Injection Analysis Based on Cerium(IV) Oxidation Sensitized by Quinine. The Analyst, 122(2), 103-106. doi:10.1039/a605703iZhang, Z., Baeyens, W. R. G., Zhang, X., Zhao, Y., & Van Der Weken, G. (1997). Chemiluminescence detection coupled to liquid chromatography for the determination of penicillamine in human urine. Analytica Chimica Acta, 347(3), 325-332. doi:10.1016/s0003-2670(97)00171-2Capitán-Vallvey, L. (2000). Chemiluminescence determination of sodium 2-mercaptoethane sulfonate by flow injection analysis using cerium(IV) sensitized by quinine. Talanta, 51(6), 1155-1161. doi:10.1016/s0039-9140(00)00291-5NIE, L., MA, H., SUN, M., LI, X., SU, M., & LIANG, S. (2003). Direct chemiluminescence determination of cysteine in human serum using quinine–Ce(IV) system. Talanta, 59(5), 959-964. doi:10.1016/s0039-9140(02)00649-5Lakowicz, J. R. (Ed.). (2006). Principles of Fluorescence Spectroscopy. doi:10.1007/978-0-387-46312-4Lookabaugh, M., & Krull, I. S. (1988). Determination of nitrite and nitrate by reversed-phase high-performance liquid chromatography using on-line post-column photolysis with ultraviolet absorbance and electrochemical detection. Journal of Chromatography A, 452, 295-308. doi:10.1016/s0021-9673(01)81454-0Gómez-Benito, C., Meseguer-Lloret, S., & Torres-Cartas, S. (2013). Sensitive determination of Fenamiphos in water samples by flow injection photoinduced chemiluminescence. International Journal of Environmental Analytical Chemistry, 93(2), 152-165. doi:10.1080/03067319.2012.663755CATALÁ-ICARDO, M., LÓPEZ-PAZ, J. L., & PEÑA-BÁDENA, A. (2011). FI-photoinduced Chemiluminescence Method for Diuron Determination in Water Samples. Analytical Sciences, 27(3), 291. doi:10.2116/analsci.27.291Hamilton, D. J., Ambrus, Á., Dieterle, R. M., Felsot, A. S., Harris, C. A., Holland, P. T., … Wong, S.-S. (2003). Regulatory limits for pesticide residues in water (IUPAC Technical Report). Pure and Applied Chemistry, 75(8), 1123-1155. doi:10.1351/pac20037508112

    Lepton Polarization and Forward-Backward Asymmetries in b -> s tau+ tau-

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    We study the spin polarizations of both tau leptons in the decay b -> s tau+ tau-. In addition to the polarization asymmetries involving a single tau, we construct asymmetries for the case where both polarizations are simultaneously measured. We also study forward-backward asymmetries with polarized tau's. We find that a large number of asymmetries are predicted to be large, >~ 10%. This permits the measurement of all Wilson coefficients and the b-quark mass, thus allowing the standard model (SM) to be exhaustively tested. Furthermore, there are many unique signals for the presence of new physics. For example, asymmetries involving triple-product correlations are predicted to be tiny within the SM, O(10^{-2}). Their observation would be a clear signal of new physics.Comment: 21 pages, LaTeX, 4 figures (included). Paper somewhat reorganized, references greatly expanded, conclusions unchange
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