Cunlu Zhao

Prof. Dr. Cunlu Zhao

Xi'an Jiaotong University, Xi'an, China
orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2008 in Journal of Colloid and Interface Science
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Journal Article
Closed access
Cunlu ZhaoCunlu Zhao
Cunlu Zhao
EZEmilijk Zholkovskij
Emilijk Zholkovskij
JMJacob H. Masliyah
Jacob H. Masliyah
CYChun Yang
Chun Yang

1 December 2013 in Advances in Colloid and Interface Science
Verified
Journal Article
Closed access
Cunlu ZhaoCunlu Zhao
Cunlu Zhao
CYChun Yang
Chun Yang

5 April 2012 in Microfluidics and Nanofluidics
Verified
Journal Article
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PDF file
Cunlu ZhaoCunlu Zhao
Cunlu Zhao
CYChun Yang
Chun Yang

1 September 2011 in Journal of Non-Newtonian Fluid Mechanics
Verified
Journal Article
Closed access
Cunlu ZhaoCunlu Zhao
Cunlu Zhao
CYChun Yang
Chun Yang

10 September 2015 in Nanoscale
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Journal Article
Open access
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Cunlu ZhaoCunlu Zhao
Cunlu Zhao
DEDaniel Ebeling
Daniel Ebeling
ISIgor Siretanu
Igor Siretanu
DEDirk van Den Ende
Dirk van Den Ende
FMFrieder Mugele
Frieder Mugele
We present a method to determine the local surface charge of solid–liquid interfaces from Atomic Force Microscopy (AFM) measurements that takes into account shifts of the adsorption/desorption equilibria of protons and ions as the cantilever tip approaches the sample. We recorded AFM force distance curves in dynamic mode with sharp tips on heterogeneous silica surfaces partially covered by gibbsite nano-particles immersed in an aqueous electrolyte with variable concentrations of dissolved NaCl and KCl at pH 5.8. Forces are analyzed in the framework of Derjaguin–Landau–Verwey–Overbeek (DLVO) theory in combination with a charge regulation boundary that describes adsorption and desorption reactions of protons and ions. A systematic method to extract the equilibrium constants of these reactions by simultaneous least-squared fitting to experimental data for various salt concentrations is developed and is shown to yield highly consistent results for silica-electrolyte interfaces. For gibbsite-electrolyte interfaces, the surface charge can be determined, yet, an unambiguous identification of the relevant surface speciation reactions is not possible, presumably due to a combination of intrinsic chemical complexity and heterogeneity of the nano-particle surfaces.

1 March 2011 in Biomicrofluidics
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Journal Article
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Cunlu ZhaoCunlu Zhao
Cunlu Zhao
CYChun Yang
Chun Yang
Electrokinetically driven microfluidic devices are usually used to analyze and process biofluids which can be classified as non-Newtonian fluids. Conventional electrokinetic theories resulting from Newtonian hydrodynamics then fail to describe the behaviors of these fluids. In this study, a theoretical analysis of electro-osmotic mobility of non-Newtonian fluids is reported. The general Cauchy momentum equation is simplified by incorporation of the Gouy–Chapman solution to the Poisson–Boltzmann equation and the Carreau fluid constitutive model. Then a nonlinear ordinary differential equation governing the electro-osmotic velocity of Carreau fluids is obtained and solved numerically. The effects of the Weissenberg number (Wi), the surface zeta potential (ψ¯s) , the power-law exponent (n) , and the transitional parameter (β) on electro-osmotic mobility are examined. It is shown that the results presented in this study for the electro-osmotic mobility of Carreau fluids are quite general so that the electro-osmotic mobility for the Newtonian fluids and the power-law fluids can be obtained as two limiting cases.