In this work, we present a new, previously unknown type of structure transformation in the high-pressure gas hydrates, which is related to the existence of two different isostructural phases of the sulfur hexafluoride clathrate hydrates. Each of these phases has its own stability field on the phase diagram. The difference between these hydrates consists of partial filling of small D cages by SF(6) molecules in the high-pressure phase; at 900 MPa, about half of small cages are occupied. Our calculations indicate that the increase of population of small cavities is improbable, therefore, at any pressure value, a part of the cavities remains vacant and the packing density is relatively low. This fact allowed us to suppose the existence of the upper pressure limit of hydrate formation in this system; the experimental results obtained confirm this assumption.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/jp061698r | DOI Listing |
ACS Omega
January 2025
Faculty of Physics and Technology, Al-Farabi Kazakh National University, Al-Farabi ave. 71/23, 050040 Almaty, Kazakhstan.
This study investigates the formation of carbon dioxide clathrate hydrates under conditions simulating interstellar environments, a process of significant astrophysical and industrial relevance. Clathrate hydrates, where gas molecules are trapped within water ice cages, play an essential role in both carbon sequestration strategies and understanding of the behavior of ices in space. We employed a combination of Fourier Transform Infrared (FTIR) spectroscopy, mass spectrometry, temperature-programmed desorption (TPD), and Density Functional Theory (DFT) calculations to explore thin films of HO:CO ice mixtures with varying CO concentrations (5-75%) prepared by vapor deposition at temperatures ranging between 11 and 180 K.
View Article and Find Full Text PDFJ Phys Chem Lett
January 2025
DST Unit of Nanoscience (DST UNS) and Thematic Unit of Excellence (TUE), Department of Chemistry, Indian Institute of Technology Madras, Chennai 600036, India.
Clathrate hydrates (CHs) are believed to exist in cold regions of space, such as comets and icy moons. While spectroscopic studies have explored their formation under similar laboratory conditions, direct structural characterization using diffraction techniques has remained elusive. We present the first electron diffraction study of tetrahydrofuran (THF) and 1,3-dioxolane (DIOX) CHs in the form of nanometer-thin ice films under an ultrahigh vacuum at cryogenic temperatures.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
Department of Petroleum Engineering, School of Energy Technology, Pandit Deendayal Energy University, Gandhinagar, Gujarat 382426, India. Electronic address:
Naturally occurring gas clathrates are a significant methane resource-the primary component of natural gas, regarded as the cleanest hydrocarbon and a key feedstock for producing gray and blue hydrogen. Despite the global abundance of gas hydrate reserves, extraction via depressurization has yet to achieve commercially viable production rates. The primary limitation lies in the low permeability of hydrate-bearing sediments, where solid clathrates obstruct porous pathways, hindering dissociation and slowing gas recovery.
View Article and Find Full Text PDFJ Chem Phys
December 2024
Division of Chemical Engineering, Graduate School of Engineering Science, Osaka University, Osaka 560-8531, Japan.
We explore the solubilities of guest CH4 and/or CO2 in the aqueous state coexisting with the corresponding hydrate. The equilibrium conditions are estimated by calculating the chemical potentials of water and guest species in the hydrate on the basis of a statistical mechanical theory using pairwise intermolecular potentials. This requires the least computational cost while covering a wide range of temperature, pressure, and composition of guest species, even for the binary hydrate.
View Article and Find Full Text PDFJ Phys Chem A
November 2024
Department of Physics, Sikkim University, Samdur, East Sikkim 737102, India.
We consider carbon monoxide (CO) confined in the hydrogen-bonded building blocks of sI and sII clathrate hydrates, viz., (5, 56, 56) cages, within the density functional theory-based calculations. We study their response to the applied electric fields in terms of changes in the geometrical parameters, dipole moment, HOMO-LUMO gap, and vibrational frequency shift.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!