NMR/MRI study of clathrate hydrate mechanisms.

نویسندگان

  • Shuqiang Gao
  • Waylon House
  • Walter G Chapman
چکیده

Clathrate hydrates are of great importance in many aspects. However, hydrate formation and dissociation mechanisms, essential to all hydrate applications, are still not well understood due to the limitations of experimental techniques capable of providing dynamic and structural information on a molecular level. NMR has been shown to be a powerful tool to noninvasively measure molecular level dynamic information. In this work, we measured nuclear magnetic resonance (NMR) spin lattice relaxation times (T1's) of tetrahydrofuran (THF) in liquid deuterium oxide (D2O) during THF hydrate formation and dissociation. At the same time, we also used magnetic resonance imaging (MRI) to monitor hydrate formation and dissociation patterns. The results showed that solid hydrate significantly influences coexisting fluid structure. Molecular evidence of residual structure was identified. Hydrate formation and dissociation mechanisms were proposed based on the NMR/MRI observations.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

A Fugacity Approach for Prediction of Phase Equilibria of Methane Clathrate Hydrate in Structure H

In this communication, a thermodynamic model is presented to predict the dissociation conditions of structure H (sH) clathrate hydrates with methane as help gas. This approach is an extension of the Klauda and Sandler fugacity model (2000) for prediction of phase boundaries of sI and sII clathrate hydrates. The phase behavior of the water and hydrocarbon system is modeled using the Peng-Robinso...

متن کامل

Spectroscopic identification, thermodynamic stability and molecular composition of hydrogen and 1,4-dioxane binary clathrate hydrate

We present the spectroscopic identification of the binary hydrogen and 1,4-dioxane clathrate hydrates in which H2 molecules are encapsulated in small cages of the structure II hydrate framework. X-ray diffraction, solid-state NMR and Raman spectroscopy were used to confirm the mixed hydrate structure and more importantly the occupancy pattern of hydrogen in clathrate cages. The corresponding pr...

متن کامل

Molecular dynamics simulation of (13)C NMR powder lineshapes of CO in structure I clathrate hydrate.

Guest molecules in nonspherical cages of inclusion compounds can possess non-uniform spatial distributions and motion. This can lead to anisotropic lineshapes in the solid-state NMR spectra of the guest species. In this work, we use our previously developed molecular dynamics-based methodology to calculate the lineshape anisotropy of guest CO species in cages of the structure I (sI) clathrate h...

متن کامل

Molecular Dynamics Simulations of Guest – Host Hydrogen Bonding in Structure I, Ii, and H Clathrate Hydrates

The standard picture is that clathrate hydrates form when hydrophobic guest molecules are compressed with water under high pressure-low temperature conditions. In the ice-like hydrate framework, water molecules form molecule-sized cavities that encapsulate the guests and minimize water-hydrophobic guest interactions. This picture, however, must be modified by observations that many water solubl...

متن کامل

Nucleation rate analysis of methane hydrate from molecular dynamics simulations.

Clathrate hydrates are solid crystalline structures most commonly formed from solutions that have nucleated to form a mixed solid composed of water and gas. Understanding the mechanism of clathrate hydrate nucleation is essential to grasp the fundamental chemistry of these complex structures and their applications. Molecular dynamics (MD) simulation is an ideal method to study nucleation at the...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • The journal of physical chemistry. B

دوره 109 41  شماره 

صفحات  -

تاریخ انتشار 2005