RESUMO
Intrusion (wetting)/extrusion (drying) of liquids in/from lyophobic nanoporous systems is key in many fields, including chromatography, nanofluidics, biology, and energy materials. Here we demonstrate that secondary topological features decorating main channels of porous systems dramatically affect the intrusion/extrusion cycle. These secondary features, allowing an unexpected bridging with liquid in the surrounding domains, stabilize the water stream intruding a micropore. This reduces the intrusion/extrusion barrier and the corresponding pressures without altering other properties of the system. Tuning the intrusion/extrusion pressures via subnanometric topological features represents a yet unexplored strategy for designing hydrophobic micropores. Though energy is not the only field of application, here we show that the proposed tuning approach may bring 20-75 MPa of intrusion/extrusion pressure increase, expanding the applicability of hydrophobic microporous materials.
Assuntos
Nanoporos , Água , Interações Hidrofóbicas e Hidrofílicas , Porosidade , Pressão , Água/químicaRESUMO
In this work, we review some physical methods of macroscopic experiments, which have been recently argued to be promising for the acquisition of valuable characteristics of biomolecular structures and interactions. The methods we focused on are electron paramagnetic resonance spectroscopy, Raman spectroscopy, and differential scanning calorimetry. They were chosen since it can be shown that they are able to provide a mutually complementary picture of the composition of cellular envelopes (with special attention paid to mycobacteria), transitions between their molecular patterning, and the response to biologically active substances (reactive oxygen species and their antagonists-antioxidants-as considered in our case study).
Assuntos
Antioxidantes , Análise Espectral Raman , Varredura Diferencial de Calorimetria , Espectroscopia de Ressonância de Spin Eletrônica , Membrana CelularRESUMO
Heat and the work of compression/decompression are among the basic properties of thermodynamic systems. Being relevant to many industrial and natural processes, this thermomechanical energy is challenging to tune due to fundamental boundaries for simple fluids. Here via direct experimental and atomistic observations, we demonstrate, for fluids consisting of nanoporous material and a liquid, one can overcome these limitations and noticeably affect both thermal and mechanical energies of compression/decompression exploiting preferential intrusion of water from aqueous solutions into subnanometer pores. We hypothesize that this effect is due to the enthalpy of dilution manifesting itself as the aqueous solution concentrates upon the preferential intrusion of pure water into pores. We suggest this genuinely subnanoscale phenomenon can be potentially a strategy for controlling the thermomechanical energy of microporous liquids and tuning the wetting/dewetting heat of nanopores relevant to a variety of natural and technological processes spanning from biomedical applications to oil-extraction and renewable energy.
RESUMO
Predicting the density of liquids at ultrahigh pressures in the case when only the data measured at ambient pressure are available is a long-standing challenge for thermodynamic research. In this work, we archived this goal for molecular liquids by applying the half-sum of the Tait equation and the Murnagnan equation in the form coordinated with Tait's at low pressure for predicting the density of molecular liquids up to the pressures more than 1 GPa with uncertainty comparable with the experimental one. It is shown that the control parameter, which is needed in addition to the initial density and the isothermal compressibility can be found using the speed of sound and the density at ambient pressure and has a clear physical interpretation in terms of the characteristic frequency of intermolecular oscillation mimicking the limiting frequency of Debye's theory of heat conductivity of solids. This fact is discussed as arguing in favour of the modern phonon theory of liquid thermodynamics and expands it range of applicability to the volumetric properties of liquids at temperatures far below the critical one. The validity of the model is illustrated with the case study of classic Bridgman's dataset as well as with some examples of ultrahigh-pressure data obtained by the diamond anvil cell and shock wave compression methods.