Raman spectroscopic studies of hydrogen clathrate hydrates
Raman spectroscopic measurements of simple hydrogen and tetrahydrofuran + hydrogen sII clathrate hydrates have been performed. Both the roton and vibron bands illuminate interesting quantum dynamics of enclathrated H 2 molecules. The complex vibron region of the Raman spectrum has been interpreted b...
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Veröffentlicht in: | The Journal of chemical physics 2009-01, Vol.130 (1), p.014506-014506-10 |
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container_title | The Journal of chemical physics |
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creator | Strobel, Timothy A. Sloan, E. Dendy Koh, Carolyn A. |
description | Raman spectroscopic measurements of simple hydrogen and
tetrahydrofuran
+
hydrogen
sII clathrate hydrates have been performed. Both the roton and vibron bands illuminate interesting quantum dynamics of enclathrated
H
2
molecules. The complex vibron region of the Raman spectrum has been interpreted by observing the change in population of these bands with temperature, measuring the absolute
H
2
content as a function of pressure, and with
D
2
isotopic substitution. Quadruple occupancy of the large sII clathrate cavity shows the highest
H
2
vibrational frequency, followed by triple and double occupancies. Singly occupied small cavities display the lowest vibrational frequency. The vibrational frequencies of
H
2
within all cavity environments are redshifted from the free gas phase value. At 76 K, the progression from ortho- to para-
H
2
occurs over a relatively slow time period (days). The rotational degeneracy of
H
2
molecules within the clathrate cavities is lifted, observed directly in splitting of the para-
H
2
roton band. Raman spectra from
H
2
and
D
2
hydrates suggest that the occupancy patterns between the two hydrates are analogous, increasing confidence that
D
2
is a suitable substitute for
H
2
. The measurements suggest that Raman is an effective and convenient method to determine the relative occupancy of hydrogen molecules in different clathrate cavities. |
doi_str_mv | 10.1063/1.3046678 |
format | Article |
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tetrahydrofuran
+
hydrogen
sII clathrate hydrates have been performed. Both the roton and vibron bands illuminate interesting quantum dynamics of enclathrated
H
2
molecules. The complex vibron region of the Raman spectrum has been interpreted by observing the change in population of these bands with temperature, measuring the absolute
H
2
content as a function of pressure, and with
D
2
isotopic substitution. Quadruple occupancy of the large sII clathrate cavity shows the highest
H
2
vibrational frequency, followed by triple and double occupancies. Singly occupied small cavities display the lowest vibrational frequency. The vibrational frequencies of
H
2
within all cavity environments are redshifted from the free gas phase value. At 76 K, the progression from ortho- to para-
H
2
occurs over a relatively slow time period (days). The rotational degeneracy of
H
2
molecules within the clathrate cavities is lifted, observed directly in splitting of the para-
H
2
roton band. Raman spectra from
H
2
and
D
2
hydrates suggest that the occupancy patterns between the two hydrates are analogous, increasing confidence that
D
2
is a suitable substitute for
H
2
. The measurements suggest that Raman is an effective and convenient method to determine the relative occupancy of hydrogen molecules in different clathrate cavities.</description><identifier>ISSN: 0021-9606</identifier><identifier>EISSN: 1089-7690</identifier><identifier>DOI: 10.1063/1.3046678</identifier><identifier>PMID: 19140621</identifier><identifier>CODEN: JCPSA6</identifier><language>eng</language><publisher>United States: American Institute of Physics</publisher><subject>Deuterium ; Furans - chemistry ; Hydrogen - chemistry ; Macromolecular Substances ; Pressure ; Spectrum Analysis, Raman ; Temperature</subject><ispartof>The Journal of chemical physics, 2009-01, Vol.130 (1), p.014506-014506-10</ispartof><rights>2009 American Institute of Physics</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-ea69b268d90ac50dcdb16f3fa43c00800f60447d9483b36708be4c97f68cd2e3</citedby><cites>FETCH-LOGICAL-c438t-ea69b268d90ac50dcdb16f3fa43c00800f60447d9483b36708be4c97f68cd2e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,790,1553,4498,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19140621$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Strobel, Timothy A.</creatorcontrib><creatorcontrib>Sloan, E. Dendy</creatorcontrib><creatorcontrib>Koh, Carolyn A.</creatorcontrib><title>Raman spectroscopic studies of hydrogen clathrate hydrates</title><title>The Journal of chemical physics</title><addtitle>J Chem Phys</addtitle><description>Raman spectroscopic measurements of simple hydrogen and
tetrahydrofuran
+
hydrogen
sII clathrate hydrates have been performed. Both the roton and vibron bands illuminate interesting quantum dynamics of enclathrated
H
2
molecules. The complex vibron region of the Raman spectrum has been interpreted by observing the change in population of these bands with temperature, measuring the absolute
H
2
content as a function of pressure, and with
D
2
isotopic substitution. Quadruple occupancy of the large sII clathrate cavity shows the highest
H
2
vibrational frequency, followed by triple and double occupancies. Singly occupied small cavities display the lowest vibrational frequency. The vibrational frequencies of
H
2
within all cavity environments are redshifted from the free gas phase value. At 76 K, the progression from ortho- to para-
H
2
occurs over a relatively slow time period (days). The rotational degeneracy of
H
2
molecules within the clathrate cavities is lifted, observed directly in splitting of the para-
H
2
roton band. Raman spectra from
H
2
and
D
2
hydrates suggest that the occupancy patterns between the two hydrates are analogous, increasing confidence that
D
2
is a suitable substitute for
H
2
. The measurements suggest that Raman is an effective and convenient method to determine the relative occupancy of hydrogen molecules in different clathrate cavities.</description><subject>Deuterium</subject><subject>Furans - chemistry</subject><subject>Hydrogen - chemistry</subject><subject>Macromolecular Substances</subject><subject>Pressure</subject><subject>Spectrum Analysis, Raman</subject><subject>Temperature</subject><issn>0021-9606</issn><issn>1089-7690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtLxDAURoMozji68A9IV4KLjjdNvEkEFzL4ggFBZh_SJHUqfdmki_n3VqcgLlx9cDkcuIeQcwpLCsiu6ZIBRxTygMwpSJUKVHBI5gAZTRUCzshJCB8AQEXGj8mMKsoBMzont2-mNk0SOm9j3wbbdqVNQhxc6UPSFsl25_r23TeJrUzc9ib6n9O44ZQcFaYK_mzaBdk8PmxWz-n69elldb9OLWcypt6gyjOUToGxN-CsyykWrDCcWQAJUCBwLpzikuUMBcjcc6tEgdK6zLMFudxru779HHyIui6D9VVlGt8OQSNKKiBTI3i1B-34SOh9obu-rE2_0xT0dydN9dRpZC8m6ZDX3v2SU5gRuNsDwZbRxLJt_rf9JNR_ErIvXOR3WQ</recordid><startdate>20090107</startdate><enddate>20090107</enddate><creator>Strobel, Timothy A.</creator><creator>Sloan, E. Dendy</creator><creator>Koh, Carolyn A.</creator><general>American Institute of Physics</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20090107</creationdate><title>Raman spectroscopic studies of hydrogen clathrate hydrates</title><author>Strobel, Timothy A. ; Sloan, E. Dendy ; Koh, Carolyn A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-ea69b268d90ac50dcdb16f3fa43c00800f60447d9483b36708be4c97f68cd2e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Deuterium</topic><topic>Furans - chemistry</topic><topic>Hydrogen - chemistry</topic><topic>Macromolecular Substances</topic><topic>Pressure</topic><topic>Spectrum Analysis, Raman</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Strobel, Timothy A.</creatorcontrib><creatorcontrib>Sloan, E. Dendy</creatorcontrib><creatorcontrib>Koh, Carolyn A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of chemical physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Strobel, Timothy A.</au><au>Sloan, E. Dendy</au><au>Koh, Carolyn A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Raman spectroscopic studies of hydrogen clathrate hydrates</atitle><jtitle>The Journal of chemical physics</jtitle><addtitle>J Chem Phys</addtitle><date>2009-01-07</date><risdate>2009</risdate><volume>130</volume><issue>1</issue><spage>014506</spage><epage>014506-10</epage><pages>014506-014506-10</pages><issn>0021-9606</issn><eissn>1089-7690</eissn><coden>JCPSA6</coden><abstract>Raman spectroscopic measurements of simple hydrogen and
tetrahydrofuran
+
hydrogen
sII clathrate hydrates have been performed. Both the roton and vibron bands illuminate interesting quantum dynamics of enclathrated
H
2
molecules. The complex vibron region of the Raman spectrum has been interpreted by observing the change in population of these bands with temperature, measuring the absolute
H
2
content as a function of pressure, and with
D
2
isotopic substitution. Quadruple occupancy of the large sII clathrate cavity shows the highest
H
2
vibrational frequency, followed by triple and double occupancies. Singly occupied small cavities display the lowest vibrational frequency. The vibrational frequencies of
H
2
within all cavity environments are redshifted from the free gas phase value. At 76 K, the progression from ortho- to para-
H
2
occurs over a relatively slow time period (days). The rotational degeneracy of
H
2
molecules within the clathrate cavities is lifted, observed directly in splitting of the para-
H
2
roton band. Raman spectra from
H
2
and
D
2
hydrates suggest that the occupancy patterns between the two hydrates are analogous, increasing confidence that
D
2
is a suitable substitute for
H
2
. The measurements suggest that Raman is an effective and convenient method to determine the relative occupancy of hydrogen molecules in different clathrate cavities.</abstract><cop>United States</cop><pub>American Institute of Physics</pub><pmid>19140621</pmid><doi>10.1063/1.3046678</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | MEDLINE; AIP Journals Complete; AIP Digital Archive; Alma/SFX Local Collection |
subjects | Deuterium Furans - chemistry Hydrogen - chemistry Macromolecular Substances Pressure Spectrum Analysis, Raman Temperature |
title | Raman spectroscopic studies of hydrogen clathrate hydrates |
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