Deuteron magnetic resonance and dielectric studies of guest reorientation and water dynamics in six clathrate hydrates containing ring-type guests
Using deuteron nuclear magnetic resonance and high-resolution dielectric spectroscopy the guest dynamics of tetrahydropyran, cyclopentane, trimethylene oxide, 1,3-dioxolane, and 1,4-dioxane clathrate hydrates is studied. By investigating lattice-deuterated as well as guest-deuterated crystals, the a...
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Published in | Journal of non-crystalline solids Vol. 407; pp. 431 - 440 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.01.2015
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Abstract | Using deuteron nuclear magnetic resonance and high-resolution dielectric spectroscopy the guest dynamics of tetrahydropyran, cyclopentane, trimethylene oxide, 1,3-dioxolane, and 1,4-dioxane clathrate hydrates is studied. By investigating lattice-deuterated as well as guest-deuterated crystals, the anisotropic guest reorientation is scrutinized and compared with previous results for tetrahydrofuran clathrate hydrate. The reorientational energy barriers depend linearly on the size of the guest molecules except for the clathrate hydrate of cyclopentane, a molecule which exhibits a dipole moment of the order of 0.01D. The ether oxygens of the other guests can induce Bjerrum L defects on the hydrate lattice. Their concentration is examined for ammonia-doped tetrahydrofuran clathrate hydrate. Covering a wide range of NH3 concentrations x, a minimal overall Bjerrum defect concentration is observed that leads to a maximum mobility on the hydrate lattice at x≈0.03%. To examine guest-induced Bjerrum L defects further, the translational motion on the undoped hydrate lattices is studied using stimulated-echo spectroscopy: The proton dynamics of CP clathrate hydrate is virtually identical to that of hexagonal ice and the water motion of THP clathrate hydrate closely matches that of the tetrahydrofuran compound.
•Clathrate hydrates containing different ring-type guests are systematically studied.•Comparison of rotational motions in guest- and lattice-deuterated crystals.•Lattice dynamics of clathrate hydrates is probed by echo spectroscopy and compared with that of hexagonal ice.•Slow host dynamics yields number of ether oxygen-induced Bjerrum L defects.•Cyclopentane's dipole moment estimated to be in the 10 to 20mD range. |
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AbstractList | Using deuteron nuclear magnetic resonance and high-resolution dielectric spectroscopy the guest dynamics of tetrahydropyran, cyclopentane, trimethylene oxide, 1,3-dioxolane, and 1,4-dioxane clathrate hydrates is studied. By investigating lattice-deuterated as well as guest-deuterated crystals, the anisotropic guest reorientation is scrutinized and compared with previous results for tetrahydrofuran clathrate hydrate. The reorientational energy barriers depend linearly on the size of the guest molecules except for the clathrate hydrate of cyclopentane, a molecule which exhibits a dipole moment of the order of 0.01D. The ether oxygens of the other guests can induce Bjerrum L defects on the hydrate lattice. Their concentration is examined for ammonia-doped tetrahydrofuran clathrate hydrate. Covering a wide range of NH3 concentrations x, a minimal overall Bjerrum defect concentration is observed that leads to a maximum mobility on the hydrate lattice at x approximately 0.03%. To examine guest-induced Bjerrum L defects further, the translational motion on the undoped hydrate lattices is studied using stimulated-echo spectroscopy: The proton dynamics of CP clathrate hydrate is virtually identical to that of hexagonal ice and the water motion of THP clathrate hydrate closely matches that of the tetrahydrofuran compound. Using deuteron nuclear magnetic resonance and high-resolution dielectric spectroscopy the guest dynamics of tetrahydropyran, cyclopentane, trimethylene oxide, 1,3-dioxolane, and 1,4-dioxane clathrate hydrates is studied. By investigating lattice-deuterated as well as guest-deuterated crystals, the anisotropic guest reorientation is scrutinized and compared with previous results for tetrahydrofuran clathrate hydrate. The reorientational energy barriers depend linearly on the size of the guest molecules except for the clathrate hydrate of cyclopentane, a molecule which exhibits a dipole moment of the order of 0.01D. The ether oxygens of the other guests can induce Bjerrum L defects on the hydrate lattice. Their concentration is examined for ammonia-doped tetrahydrofuran clathrate hydrate. Covering a wide range of NH3 concentrations x, a minimal overall Bjerrum defect concentration is observed that leads to a maximum mobility on the hydrate lattice at x≈0.03%. To examine guest-induced Bjerrum L defects further, the translational motion on the undoped hydrate lattices is studied using stimulated-echo spectroscopy: The proton dynamics of CP clathrate hydrate is virtually identical to that of hexagonal ice and the water motion of THP clathrate hydrate closely matches that of the tetrahydrofuran compound. •Clathrate hydrates containing different ring-type guests are systematically studied.•Comparison of rotational motions in guest- and lattice-deuterated crystals.•Lattice dynamics of clathrate hydrates is probed by echo spectroscopy and compared with that of hexagonal ice.•Slow host dynamics yields number of ether oxygen-induced Bjerrum L defects.•Cyclopentane's dipole moment estimated to be in the 10 to 20mD range. |
Author | Böhmer, R. Ihrig, A. Kibies, P. Kast, S.M. Kahlau, R. Nelson, H. |
Author_xml | – sequence: 1 givenname: H. surname: Nelson fullname: Nelson, H. email: Helge.Nelson@tu-dortmund.de organization: Fakultät Physik, Technische Universität Dortmund, 44221 Dortmund, Germany – sequence: 2 givenname: A. surname: Ihrig fullname: Ihrig, A. organization: Fakultät Physik, Technische Universität Dortmund, 44221 Dortmund, Germany – sequence: 3 givenname: R. surname: Kahlau fullname: Kahlau, R. organization: Physikalisches Institut, Universität Bayreuth, 95540 Bayreuth, Germany – sequence: 4 givenname: P. surname: Kibies fullname: Kibies, P. organization: Fakultät für Chemie und Chemische Biologie, Technische Universität Dortmund, 44221 Dortmund, Germany – sequence: 5 givenname: S.M. surname: Kast fullname: Kast, S.M. organization: Fakultät für Chemie und Chemische Biologie, Technische Universität Dortmund, 44221 Dortmund, Germany – sequence: 6 givenname: R. surname: Böhmer fullname: Böhmer, R. organization: Fakultät Physik, Technische Universität Dortmund, 44221 Dortmund, Germany |
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CitedBy_id | crossref_primary_10_1021_acs_jpcb_5b08369 crossref_primary_10_1021_acs_jpcc_8b05314 crossref_primary_10_1103_PhysRevB_94_184306 crossref_primary_10_1039_D3CP02774K crossref_primary_10_1063_1_5093973 crossref_primary_10_1016_j_physrep_2014_07_005 crossref_primary_10_1021_acs_energyfuels_2c01723 crossref_primary_10_1070_RCR4986 crossref_primary_10_1021_acs_jpcb_5b10034 crossref_primary_10_1021_acs_jpcb_7b00033 crossref_primary_10_1039_D4CP01656D crossref_primary_10_1039_D2CP05799A |
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Snippet | Using deuteron nuclear magnetic resonance and high-resolution dielectric spectroscopy the guest dynamics of tetrahydropyran, cyclopentane, trimethylene oxide,... |
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SubjectTerms | Clathrate hydrates Crystal defects Deuterons Dynamic tests Dynamics Hydrates Hydrogen bonds Lattices Nuclear magnetic resonance Tetrahydrofuran |
Title | Deuteron magnetic resonance and dielectric studies of guest reorientation and water dynamics in six clathrate hydrates containing ring-type guests |
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