147 research outputs found
A Liv\v{s}ic-type theorem and some regularity properties for nonadditive sequences of potentials
We study some notions of cohomology for asymptotically additive sequences and
prove a Liv\v{s}ic-type result for almost additive sequences of potentials. As
a consequence, we are able to characterize almost additive sequences based on
their equilibrium measures and also show the existence of almost (and
asymptotically) additive sequences of H\"older continuous functions satisfying
the bounded variation condition (with a unique equilibrium measure) and which
are not physically equivalent to any additive sequence generated by a H\"older
continuous function. None of these examples were previously known, even in the
case of full shifts of finite type. Moreover, we also use our main result to
suggest a classification of almost additive sequences based on physical
equivalence relations with respect to the classical additive setup.Comment: 36 page
Nonadditive families of potentials: physical equivalence and some regularity relations
We show that additive and asymptotically additive families of continuous
functions with respect to suspension flows are physically equivalent. In
particular, the equivalence result holds for hyperbolic flows and some classes
of expansive flows in general. Moreover, we show how this equivalence result
can be used to extend the nonadditive thermodynamic formalism and multifractal
analysis. In the second part of this work, we obtain a Liv\v{s}ic-like result
for nonadditive families of potentials and also address the H\"older and Bowen
regularity problem for the physical equivalence relations with respect to
hyperbolic symbolic flows.Comment: This material is a substantial upgrade on the previous submission
"Asymptotically additive families of functions and a physical equivalence
problem for flows" (68 pages
Hyperbolicity and Recurrence in Dynamical Systems: A Survey of Recent ResuIts
We discuss selected topics of current research interest in the theory of dynamical systems, with emphasis on dimension theory, multifractal analysis, and quantitative recurrence
Residual Multiparticle Entropy for a Fractal Fluid of Hard Spheres
The residual multiparticle entropy (RMPE) of a fluid is defined as the
difference, , between the excess entropy per particle (relative to an
ideal gas with the same temperature and density), , and the
pair-correlation contribution, . Thus, the RMPE represents the net
contribution to due to spatial correlations involving three,
four, or more particles. A heuristic `ordering' criterion identifies the
vanishing of the RMPE as an underlying signature of an impending structural or
thermodynamic transition of the system from a less ordered to a more spatially
organized condition (freezing is a typical example). Regardless of this, the
knowledge of the RMPE is important to assess the impact of non-pair
multiparticle correlations on the entropy of the fluid. Recently, an accurate
and simple proposal for the thermodynamic and structural properties of a
hard-sphere fluid in fractional dimension has been proposed [Santos,
A.; L\'opez de Haro, M. \emph{Phys. Rev. E} \textbf{2016}, \emph{93}, 062126].
The aim of this work is to use this approach to evaluate the RMPE as a function
of both and the packing fraction . It is observed that, for any given
dimensionality , the RMPE takes negative values for small densities, reaches
a negative minimum at a packing fraction
, and then rapidly increases, becoming positive beyond a
certain packing fraction . Interestingly, while both
and monotonically decrease as dimensionality
increases, the value of exhibits a nonmonotonic
behavior, reaching an absolute minimum at a fractional dimensionality . A plot of the scaled RMPE shows a
quasiuniversal behavior in the region .Comment: 10 pages, 3 figures; v2: minor change
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The Nonadditive Generalization of Klimontovich's S-Theorem for Open Systems and Boltzmann's Orthodes
We show that the nonadditive open systems can be studied in a consistent manner by using a generalized version of S-theorem. This new generalized S-theorem can further be considered as an indication of self-organization in nonadditive open systems as prescribed by Haken. The nonadditive S-theorem is then illustrated by using the modified Van der Pol oscillator. Finally, Tsallis entropy as an equilibrium entropy is studied by using Boltzmann's method of orthodes. This part of dissertation shows that Tsallis ensemble is on equal footing with the microcanonical, canonical and grand canonical ensembles. However, the associated entropy turns out to be Renyi entropy
Network Topology in Water Nanoconfined between Phospholipid Membranes
Water provides the driving force for the assembly and stability of many cellular components. Despite its impact on biological functions, a nanoscale understanding of the relationship between its structure and dynamics under soft confinement has remained elusive. As expected, water in contact with biological membranes recovers its bulk density and dynamics at ∼1 nm from phospholipid headgroups but surprisingly enhances its intermediate range order (IRO) over a distance, at least, twice as large. Here, we explore how the IRO is related to the water’s hydrogen-bond network (HBN) and its coordination defects. We characterize the increased IRO by an alteration of the HBN up to more than eight coordination shells of hydration water. The HBN analysis emphasizes the existence of a bound–unbound water interface at ∼0.8 nm from the membrane. The unbound water has a distribution of defects intermediate between bound and bulk water, but with density and dynamics similar to bulk, while bound water has reduced thermal energy and many more HBN defects than low-temperature water. This observation could be fundamental for developing nanoscale models of biological interactions and for understanding how alteration of the water structure and topology, for example, due to changes in extracellular ions concentration, could affect diseases and signaling. More generally, it gives us a different perspective to study nanoconfined water
Fabrications and Applications of Micro/nanofluidics in Oil and Gas Recovery: A Comprehensive Review
Understanding fluid flow characteristics in porous medium, which determines the development of oil and gas oilfields, has been a significant research subject for decades. Although using core samples is still essential, micro/nanofluidics have been attracting increasing attention in oil recovery fields since it offers direct visualization and quantification of fluid flow at the pore level. This work provides the latest techniques and development history of micro/nanofluidics in oil and gas recovery by summarizing and discussing the fabrication methods, materials and corresponding applications. Compared with other reviews of micro/nanofluidics, this comprehensive review is in the perspective of solving specific issues in oil and gas industry, including fluid characterization, multiphase fluid flow, enhanced oil recovery mechanisms, and fluid flow in nano-scale porous media of unconventional reservoirs, by covering most of the representative visible studies using micro/nanomodels. Finally, we present the challenges of applying micro/nanomodels and future research directions based on the work
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