Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12104/44906
Title: Temporal evolution of the size distribution during exchange kinetics of pluronic P103 at low temperatures
Author: Sevilla-Escoboza, R.
Buldu, J.M.
Pisarchik, A.N.
Boccaletti, S.
Gutierrez, R.
Issue Date: 2015
Abstract: We propose a methodology to analyze synchronization in an ensemble of diffusively coupled multistable systems. First, we study how two bidirectionally coupled multistable oscillators synchronize and demonstrate the high complexity of the basins of attraction of coexisting synchronous states. Then, we propose the use of the master stability function (MSF) for multistable systems to describe synchronizability, even during intermittent behavior, of a network of multistable oscillators, regardless of both the number of coupled oscillators and the interaction structure. In particular, we show that a network of multistable elements is synchronizable for a given range of topology spectra and coupling strengths, irrespective of specific attractor dynamics to which different oscillators are locked, and even in the presence of intermittency. Finally, we experimentally demonstrate the feasibility and robustness of the MSF approach with a network of multistable electronic circuits. " 2015 American Physical Society.",,,,,,"10.1103/PhysRevE.91.032902",,,"http://hdl.handle.net/20.500.12104/44906","http://www.scopus.com/inward/record.url?eid=2-s2.0-84924787048&partnerID=40&md5=dc4f4cb65288d03a465bf820ee1fc10d
http://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&D=prem&AN=25871167",,,,,,"3",,"Physical Review E - Statistical, Nonlinear, and Soft Matter Physics",,,,"91",,"Scopus
WOS
MEDLINE",,,,"Index Medicus",,,,,,,,"Synchronization of intermittent behavior in ensembles of multistable dynamical systems",,"Article" "46724","123456789/35008","Escalante, J.I., Depto. de Ing. Química, Universidad de Guadalajara, Boul. M. García Barragan #1451, Guadalajara, Jalisco 44430, Mexico; Rodríguez-Guadarrama, L.A., Depto. de Ing. Química, Universidad de Guadalajara, Boul. M. García Barragan #1451, Guadalajara, Jalisco 44430, Mexico; Mendizábal, E., Depto. de Ing. Química, Universidad de Guadalajara, Boul. M. García Barragan #1451, Guadalajara, Jalisco 44430, Mexico; Puig, J.E., Depto. de Ing. Química, Universidad de Guadalajara, Boul. M. García Barragan #1451, Guadalajara, Jalisco 44430, Mexico; López, R.G., Ctro. de Invest. en Quim. Aplicada, Saltillo, Coahuila 25100, Mexico; Katime, I., Depto. de Quim. Física, Facultad de Ciencias, Universidad del País Vasco, Bilbao, Spain
Mendizábal, E. M., Universidad de Guadalajara. Centro Universitario de Ciencias Exactas e Ingenierías",,"Escalante, J.I.
Rodriguez-Guadarrama, L.A.
Mendizábal, E. M.
Puig, J.E.
Lopez, R.G.
Katime, I.",,"1996",,"The polymerization of butyl methacrylate in three-component microemulsions prepared with the cationic surfactant dodecyltrimethylammonium bromide is reported here as a function of monomer and surfactant content in parent microemulsions, type and concentration of initiator, and temperature. Fast reaction rates and high conversions are achieved in all cases. Final latexes are bluish-opaque and stable, and contain spherical particles with diameters in the range of 20 to 30 nm, depending on composition of the parent microemulsions and reaction conditions. Each of these particles is composed of a few macromolecules of high molecular weight (2 to 4 106 Dalton). Both particle size and average molecular weight remain constant throughout the reaction, suggesting a continuous nucleation mechanism. Analysis of the molecular weight distribution indicates that the controlling termination mechanism is chain-transfer to monomer. © 1996 John Wiley & Sons, Inc.",,,,,,,,,,"http://www.scopus.com/inward/record.url?eid=2-s2.0-0030285163&partnerID=40&md5=0dddc1346708e0967377b9dc6227a24b
http://hdl.handle.net/20.500.12104/44945",,,,,,"9",,"Journal of Applied Polymer Science",,"1313
1323",,"62",,"Scopus
WOS",,,,,,,,,,"Synthesis of poly(butyl methacrylate) in three-component cationic microemulsions",,,,"Article", "46767","123456789/35008",,"Fernandez, V.V.A., Laboratoire de Rhéologie, UJF/INPG/CNRS, UMR 5520, B.P.53, F-38041 Grenoble Cedex 9, France, Departamentos de Ingeniería Química, UniVersidad de Guadalajara, Boul. M. García Barragán # 1451, Guadalajara, Jal. 44430, Mexico; Soltero, J.F.A., Laboratoire de Rhéologie, UJF/INPG/CNRS, UMR 5520, B.P.53, F-38041 Grenoble Cedex 9, France, Departamentos de Ingeniería Química, UniVersidad de Guadalajara, Boul. M. García Barragán # 1451, Guadalajara, Jal. 44430, Mexico; Puig, J.E., Departamentos de Ingeniería Química, UniVersidad de Guadalajara, Boul. M. García Barragán # 1451, Guadalajara, Jal. 44430, Mexico; Rharbi, Y., Laboratoire de Rhéologie, UJF/INPG/CNRS, UMR 5520, B.P.53, F-38041 Grenoble Cedex 9, France",,"Fernandez, V.V.A.
Soltero, J.F.A.
Puig, J.E.
Rharbi, Y.",,"2009",,"The micellar dynamics of many (PEO-PPO-PEO) triblock copolymers have been extensively investigated throughout the past decade using ultrasonic relaxation or temperature jump experiments. These methods primarily use the total scattering intensity to quantify the exchange mechanisms, and these results are then interpreted to get an idea about temporal evolution of the micelle size and size distribution. In this paper, we present experiments where we directly measure the size of the micelles and the size distribution during the exchange kinetic of the pluronic triblock copolymer P103. Solutions of the commercial P103 surfactant form premicelle aggregates in the proximity of the critical micelle temperature and proper micelles at high temperatures. The kinetics of evolution from aggregates to proper micelles is investigated using dynamic light scattering after a temperature jump. The temporal evolution of the scattering intensity and the average size as well as the size distribution were used to discuss the possible exchange mechanisms. " 2009 American Chemical Society.
URI: http://hdl.handle.net/20.500.12104/44988
http://www.scopus.com/inward/record.url?eid=2-s2.0-65249190874&partnerID=40&md5=9d418ec948ce24af4bd6c8400e506dc1
http://dx.doi.org/10.1021/jp809685q
Appears in Collections:Producción científica UdeG

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