More Like this

1. Non-simple conformal loop ensembles on Liouville quantum gravity and the law of CLE percolation interfaces

   https://doi.org/10.1007/s00440-021-01070-4  

   Miller, Jason ; Sheffield, Scott ; Werner, Wendelin ( June 2021 , Probability Theory and Related Fields)

   We study the structure of the Liouville quantum gravity (LQG) surfaces that are cut out as one explores a conformal loop-ensemble$$\hbox {CLE}_{\kappa '}$$${\text{CLE}}_{{\kappa }^{\prime }}$for$$\kappa '$$${\kappa }^{\prime }$in (4, 8) that is drawn on an independent$$\gamma $$$\gamma$-LQG surface for$$\gamma ^2=16/\kappa '$$${\gamma }^2=16/{\kappa }^{\prime }$. The results are similar in flavor to the ones from our companion paper dealing with$$\hbox {CLE}_{\kappa }$$${\text{CLE}}_{\kappa }$for$$\kappa $$$\kappa$in (8/3, 4), where the loops of the CLE are disjoint and simple. In particular, we encode the combined structure of the LQG surface and the$$\hbox {CLE}_{\kappa '}$$${\text{CLE}}_{{\kappa }^{\prime }}$in terms of stable growth-fragmentation trees or their variants, which also appear in the asymptotic study of peeling processes on decorated planar maps. This has consequences for questions that do a priori not involve LQG surfaces: In our paper entitled “CLE Percolations” described the law of interfaces obtained when coloring the loops of a$$\hbox {CLE}_{\kappa '}$$${\text{CLE}}_{{\kappa }^{\prime }}$independently into two colors with respective probabilitiespand$$1-p$$$1-p$. This description was complete up to one missing parameter$$\rho $$$\rho$. The results of the present paper about CLE on LQG allow us to determine its value in terms ofpand$$\kappa '$$${\kappa }^{\prime }$. It shows in particular that$$\hbox {CLE}_{\kappa '}$$${\text{CLE}}_{{\kappa }^{\prime }}$and$$\hbox {CLE}_{16/\kappa '}$$${\text{CLE}}_{16/{\kappa }^{\prime }}$are related via a continuum analog of the Edwards-Sokal coupling between$$\hbox {FK}_q$$${\text{FK}}_q$percolation and theq-state Potts model (which makes sense evenmore »for non-integerqbetween 1 and 4) if and only if$$q=4\cos ^2(4\pi / \kappa ')$$$q=4{cos}^2(4\pi /{\kappa }^{\prime })$. This provides further evidence for the long-standing belief that$$\hbox {CLE}_{\kappa '}$$${\text{CLE}}_{{\kappa }^{\prime }}$and$$\hbox {CLE}_{16/\kappa '}$$${\text{CLE}}_{16/{\kappa }^{\prime }}$represent the scaling limits of$$\hbox {FK}_q$$${\text{FK}}_q$percolation and theq-Potts model whenqand$$\kappa '$$${\kappa }^{\prime }$are related in this way. Another consequence of the formula for$$\rho (p,\kappa ')$$$\rho (p,{\kappa }^{\prime })$is the value of half-plane arm exponents for such divide-and-color models (a.k.a. fuzzy Potts models) that turn out to take a somewhat different form than the usual critical exponents for two-dimensional models.

   « less
2. QLBT: a linear Boltzmann transport model for heavy quarks in a quark-gluon plasma of quasi-particles

   https://doi.org/10.1140/epjc/s10052-022-10308-x  

   Liu, Feng-Lei ; Xing, Wen-Jing ; Wu, Xiang-Yu ; Qin, Guang-You ; Cao, Shanshan ; Wang, Xin-Nian ( April 2022 , The European Physical Journal C)

   We develop a new heavy quark transport model, QLBT, to simulate the dynamical propagation of heavy quarks inside the quark-gluon plasma (QGP) created in relativistic heavy-ion collisions. Our QLBT model is based on the linear Boltzmann transport (LBT) model with the ideal QGP replaced by a collection of quasi-particles to account for the non-perturbative interactions among quarks and gluons of the hot QGP. The thermal masses of quasi-particles are fitted to the equation of state from lattice QCD simulations using the Bayesian statistical analysis method. Combining QLBT with our advanced hybrid fragmentation-coalescence hadronization approach, we calculate the nuclear modification factor$$R_\mathrm {AA}$$$R_{\mathrm{AA}}$and the elliptic flow$$v_2$$$v_2$ofDmesons at the Relativistic Heavy-Ion Collider and the Large Hadron Collider. By comparing our QLBT calculation to the experimental data on theDmeson$$R_\mathrm {AA}$$$R_{\mathrm{AA}}$and$$v_2$$$v_2$, we extract the heavy quark transport parameter$$\hat{q}$$$\hat{q}$and diffusion coefficient$$D_\mathrm {s}$$$D_s$in the temperature range of$$1-4~T_\mathrm {c}$$$1-4T_c$, and compare them with the lattice QCD results and other phenomenological studies.
3. A simple analytic model for predicting the wicking velocity in micropillar arrays

   https://doi.org/10.1038/s41598-019-56361-7  

   Krishnan, Siva Rama ; Bal, John ; Putnam, Shawn A. ( December 2019 , Scientific Reports)

   Hemiwicking is the phenomena where a liquid wets a textured surface beyond its intrinsic wetting length due to capillary action and imbibition. In this work, we derive a simple analytical model for hemiwicking in micropillar arrays. The model is based on the combined effects of capillary action dictated by interfacial and intermolecular pressures gradients within the curved liquid meniscus and fluid drag from the pillars at ultra-low Reynolds numbers$${\boldsymbol{(}}{{\bf{10}}}^{{\boldsymbol{-}}{\bf{7}}}{\boldsymbol{\lesssim }}{\bf{Re}}{\boldsymbol{\lesssim }}{{\bf{10}}}^{{\boldsymbol{-}}{\bf{3}}}{\boldsymbol{)}}$$$\left({10}^{-7}\lesssim \mathrm{Re}\lesssim {10}^{-3}\right)$. Fluid drag is conceptualized via a critical Reynolds number:$${\bf{Re}}{\boldsymbol{=}}\frac{{{\bf{v}}}_{{\bf{0}}}{{\bf{x}}}_{{\bf{0}}}}{{\boldsymbol{\nu }}}$$$\mathrm{Re}=\frac{v_0{x}_0}{\nu }$, wherev₀corresponds to the maximum wetting speed on a flat, dry surface andx₀is the extension length of the liquid meniscus that drives the bulk fluid toward the adsorbed thin-film region. The model is validated with wicking experiments on different hemiwicking surfaces in conjunction withv₀andx₀measurements using Water$${\boldsymbol{(}}{{\bf{v}}}_{{\bf{0}}}{\boldsymbol{\approx }}{\bf{2}}\,{\bf{m}}{\boldsymbol{/}}{\bf{s}}{\boldsymbol{,}}\,{\bf{25}}\,{\boldsymbol{\mu }}{\bf{m}}{\boldsymbol{\lesssim }}{{\bf{x}}}_{{\bf{0}}}{\boldsymbol{\lesssim }}{\bf{28}}\,{\boldsymbol{\mu }}{\bf{m}}{\boldsymbol{)}}$$$\left(v_0\approx 2m/s,25\mu m\lesssim x_0\lesssim 28\mu m\right)$, viscous FC-70$${\boldsymbol{(}}{{\boldsymbol{v}}}_{{\bf{0}}}{\boldsymbol{\approx }}{\bf{0.3}}\,{\bf{m}}{\boldsymbol{/}}{\bf{s}}{\boldsymbol{,}}\,{\bf{18.6}}\,{\boldsymbol{\mu }}{\bf{m}}{\boldsymbol{\lesssim }}{{\boldsymbol{x}}}_{{\bf{0}}}{\boldsymbol{\lesssim }}{\bf{38.6}}\,{\boldsymbol{\mu }}{\bf{m}}{\boldsymbol{)}}$$$\left(v_0\approx 0.3m/s,18.6\mu m\lesssim x_0\lesssim 38.6\mu m\right)$and lower viscosity Ethanol$${\boldsymbol{(}}{{\boldsymbol{v}}}_{{\bf{0}}}{\boldsymbol{\approx }}{\bf{1.2}}\,{\bf{m}}{\boldsymbol{/}}{\bf{s}}{\boldsymbol{,}}\,{\bf{11.8}}\,{\boldsymbol{\mu }}{\bf{m}}{\boldsymbol{\lesssim }}{{\bf{x}}}_{{\bf{0}}}{\boldsymbol{\lesssim }}{\bf{33.3}}\,{\boldsymbol{\mu }}{\bf{m}}{\boldsymbol{)}}$$$\left(v_0\approx 1.2m/s,11.8\mu m\lesssim x_0\lesssim 33.3\mu m\right)$.
4. Evaporation-controlled dripping-onto-substrate (DoS) extensional rheology of viscoelastic polymer solutions

   https://doi.org/10.1038/s41598-022-08448-x  

   Robertson, Benjamin P. ; Calabrese, Michelle A. ( March 2022 , Scientific Reports)

   Extensional flow properties of polymer solutions in volatile solvents govern many industrially-relevant coating processes, but existing instrumentation lacks the environment necessary to control evaporation. To mitigate evaporation during dripping-onto-substrate (DoS) extensional rheology measurements, we developed a chamber to enclose the sample in an environment saturated with solvent vapor. We validated the evaporation-controlled DoS device by measuring a model high molecular weight polyethylene oxide (PEO) in various organic solvents both inside and outside of the chamber. Evaporation substantially increased the extensional relaxation time$$\lambda _{E}$$${\lambda }_E$for PEO in volatile solvents like dichloromethane and chloroform. PEO/chloroform solutions displayed an over 20-fold increase in$$\lambda _{E}$$${\lambda }_E$due to the formation of an evaporation-induced surface film; evaporation studies confirmed surface features and skin formation reminiscent of buckling instabilities commonly observed in drying polymer solutions. Finally, the relaxation times of semi-dilute PEO/chloroform solutions were measured with environmental control, where$$\lambda _{E}$$${\lambda }_E$scaled with concentration by the exponent$$m=0.62$$$m=0.62$. These measurements validate the evaporation-controlled DoS environment, and confirm that chloroform is a good solvent for PEO, with a Flory exponent of$$\nu =0.54$$$\nu =0.54$. Our results are the first to control evaporation during DoS extensional rheology, and provide guidelines establishing when environmental control is necessary to obtain accurate rheological parameters.
5. Polarization tensor of magnetized quark-gluon plasma at nonzero baryon density

   https://doi.org/10.1140/epjc/s10052-021-09650-3  

   Wang, Xinyang ; Shovkovy, Igor ( October 2021 , The European Physical Journal C)

   We derive a general expression for the absorptive part of the one-loop photon polarization tensor in a strongly magnetized quark-gluon plasma at nonzero baryon chemical potential. To demonstrate the application of the main result in the context of heavy-ion collisions, we study the effect of a nonzero baryon chemical potential on the photon emission rate. The rate and the ellipticity of photon emission are studied numerically as a function the transverse momentum (energy) for several values of temperature and chemical potential. When the chemical potential is small compared to the temperature, the rates of the quark and antiquark splitting processes (i.e.,$$q\rightarrow q +\gamma $$$q\to q+\gamma$and$${\bar{q}}\rightarrow {\bar{q}} +\gamma $$$\overline{q}\to \overline{q}+\gamma$, respectively) are approximately the same. However, the quark splitting gradually becomes the dominant process with increasing the chemical potential. We also find that increasing the chemical potential leads to a growing total photon production rate but has only a small effect on the ellipticity of photon emission. The quark-antiquark annihilation ($$q+{\bar{q}}\rightarrow \gamma $$$q+\overline{q}\to \gamma$) also contributes to the photon production, but its contribution remains relatively small for a wide range of temperatures and chemical potentials investigated.