Wikipedia

Clathrate hydrate

Clathrate hydrates, or gas hydrates, clathrates, or hydrates, are crystalline water-based solids physically resembling ice, in which small non-polar molecules (typically gases) or polar molecules with large hydrophobic moieties are trapped inside "cages" of hydrogen bonded, frozen water molecules.[1][2] In other words, clathrate hydrates are clathrate compounds in which the host molecule is water and the guest molecule is typically a gas or liquid. Without the support of the trapped molecules, the lattice structure of hydrate clathrates would collapse into conventional ice crystal structure or liquid water. Most low molecular weight gases, including O2, H2, N2, CO2, CH4, H2S, Ar, Kr, Xe, and Cl2 as well as some higher hydrocarbons and freons, will form hydrates at suitable temperatures and pressures. Clathrate hydrates are not officially chemical compounds, as the enclathrated guest molecules are never bonded to the lattice. The formation and decomposition of clathrate hydrates are first order phase transitions, not chemical reactions. Their detailed formation and decomposition mechanisms on a molecular level are still not well understood.[3][4][5] Clathrate hydrates were first documented in 1810 by Sir Humphry Davy who found that water was a primary component of what was earlier thought to be solidified chlorine.[6][7]

Methane clathrate block embedded in the sediment of hydrate ridge, off Oregon, USA

Clathrates have been found to occur naturally in large quantities. Around 6.4 trillion (6.4×1012) tonnes of methane is trapped in deposits of methane clathrate on the deep ocean floor.[8] Such deposits can be found on the Norwegian continental shelf in the northern headwall flank of the Storegga Slide. Clathrates can also exist as permafrost, as at the Mallik gas hydrate site in the Mackenzie Delta of northwestern Canadian Arctic. These natural gas hydrates are seen as a potentially vast energy resource and several countries have dedicated national programs to develop this energy resource.[9] Clathrate hydrate has also been of great interest as technology enabler for many applications like seawater desalination,[10] gas storage,[11] carbon dioxide capture & storage,[12] cooling medium for data centre[13] and district cooling etc. Hydrocarbon clathrates cause problems for the petroleum industry, because they can form inside gas pipelines, often resulting in obstructions. Deep sea deposition of carbon dioxide clathrate has been proposed as a method to remove this greenhouse gas from the atmosphere and control climate change. Clathrates are suspected to occur in large quantities on some outer planets, moons and trans-Neptunian objects, binding gas at fairly high temperatures.[14]

History and etymology

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Clathrate hydrates were discovered in 1810 by Humphry Davy.[15] Clathrates were studied by P. Pfeiffer in 1927 and in 1930, E. Hertel defined "molecular compounds" as substances decomposed into individual components following the mass action law in solution or gas state. Clathrate hydrates were discovered to form blockages in gas pipelines in 1934 by Hammerschmidt that led to increase in research to avoid hydrate formation.[16] In 1945, H. M. Powell analyzed the crystal structure of these compounds and named them clathrates. Gas production through methane hydrates has since been realized and has been tested for energy production in Japan and China.[17]

The word clathrate is derived from the Latin clathratus (clatratus), meaning 'with bars, latticed'.[18]

Structure

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Cages building the different gas hydrate structures

Gas hydrates usually form two crystallographic cubic structures: structure (Type) I (named sI) and structure (Type) II (named sII)[19] of space groups   and   respectively. A third hexagonal structure of space group   may also be observed (Type H).[20]

The unit cell of Type I consists of 46 water molecules, forming two types of cages – small and large. The unit cell contains two small cages and six large ones. The small cage has the shape of a pentagonal dodecahedron (512) (which is not a regular dodecahedron) and the large one that of a tetradecahedron, specifically a hexagonal truncated trapezohedron (51262). Together, they form a version of the Weaire–Phelan structure. Typical guests forming Type I hydrates are CO2 in carbon dioxide clathrate and CH4 in methane clathrate.

The unit cell of Type II consists of 136 water molecules, again forming two types of cages – small and large. In this case there are sixteen small cages and eight large ones in the unit cell. The small cage again has the shape of a pentagonal dodecahedron (512), but the large one is a hexadecahedron (51264). Type II hydrates are formed by gases like O2 and N2.

The unit cell of Type H consists of 34 water molecules, forming three types of cages – two small ones of different types, and one "huge". In this case, the unit cell consists of three small cages of type 512, two small ones of type 435663 and one huge of type 51268. The formation of Type H requires the cooperation of two guest gases (large and small) to be stable. It is the large cavity that allows structure H hydrates to fit in large molecules (e.g. butane, hydrocarbons), given the presence of other smaller help gases to fill and support the remaining cavities. Structure H hydrates were suggested to exist in the Gulf of Mexico. Thermogenically produced supplies of heavy hydrocarbons are common there.

The molar fraction of water of most clathrate hydrates is 85%. Clathrate hydrates are derived from organic hydrogen-bonded frameworks. These frameworks are prepared from molecules that "self-associate" by multiple hydrogen-bonding interactions. Small molecules or gases (i.e. methane, carbon dioxide, hydrogen) can be encaged as a guest in hydrates. The ideal guest/host ratio for clathrate hydrates range from 0.8 to 0.9. The guest interaction with the host is limited to van der Waals forces. Certain exceptions exist in semiclathrates where guests incorporate into the host structure via hydrogen bonding with the host structure. Hydrates form often with partial guest filling and collapse in the absence of guests occupying the water cages. Like ice, clathrate hydrates are stable at low temperatures and high pressure and possess similar properties like electrical resistivity. Clathrate hydrates are naturally occurring and can be found in the permafrost and oceanic sediments. Hydrates can also be synthesized through seed crystallization or using amorphous precursors for nucleation.[17]


 
Portion of the lattice of the clathrate xenon-paraquinol.[21]

Clathrates have been explored for many applications including: gas storage, gas production, gas separation, desalination, thermoelectrics, photovoltaics, and batteries.

Hydrates on Earth

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Natural gas hydrates

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Main article: Methane clathrate

Naturally on Earth gas hydrates can be found on the seabed, in ocean sediments,[22] in deep lake sediments (e.g. Lake Baikal), as well as in the permafrost regions. The amount of methane potentially trapped in natural methane hydrate deposits may be significant (1015 to 1017 cubic metres),[23] which makes them of major interest as a potential energy resource. Catastrophic release of methane from the decomposition of such deposits may lead to a global climate change, referred to as the "clathrate gun hypothesis", because CH4 is a more potent greenhouse gas than CO2 (see Atmospheric methane). The fast decomposition of such deposits is considered a geohazard, due to its potential to trigger landslides, earthquakes and tsunamis. However, natural gas hydrates do not contain only methane but also other hydrocarbon gases, as well as H2S and CO2. Air hydrates are frequently observed in polar ice samples.

Pingos are common structures in permafrost regions.[24] Similar structures are found in deep water related to methane vents. Significantly, gas hydrates can even be formed in the absence of a liquid phase. Under that situation, water is dissolved in gas or in liquid hydrocarbon phase.[25]

In 2017, both Japan and China announced that attempts at large-scale resource extraction of methane hydrates from under the seafloor were successful. However, commercial-scale production remains years away.[26][27]

The 2020 Research Fronts report identified gas hydrate accumulation and mining technology as one of the top 10 research fronts in the geosciences.[28]

Gas hydrates in pipelines

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Thermodynamic conditions favouring hydrate formation are often found in pipelines. This is highly undesirable, because the clathrate crystals might agglomerate and plug the line[29] and cause flow assurance failure and damage valves and instrumentation. The results can range from flow reduction to equipment damage.

Hydrate formation, prevention and mitigation philosophy

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Hydrates have a strong tendency to agglomerate and to adhere to the pipe wall and thereby plug the pipeline. Once formed, they can be decomposed by increasing the temperature and/or decreasing the pressure. Even under these conditions, the clathrate dissociation is a slow process.

Therefore, preventing hydrate formation appears to be the key to the problem. A hydrate prevention philosophy could typically be based on three levels of security, listed in order of priority:

  1. Avoid operational conditions that might cause formation of hydrates by depressing the hydrate formation temperature using glycol dehydration;
  2. Temporarily change operating conditions in order to avoid hydrate formation;
  3. Prevent formation of hydrates by addition of chemicals that (a) shift the hydrate equilibrium conditions towards lower temperatures and higher pressures or (b) increase hydrate formation time (inhibitors)

The actual philosophy would depend on operational circumstances such as pressure, temperature, type of flow (gas, liquid, presences of water etc.).

Hydrate inhibitors

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When operating within a set of parameters where hydrates could be formed, there are still ways to avoid their formation. Altering the gas composition by adding chemicals can lower the hydrate formation temperature and/or delay their formation. Two options generally exist:

The most common thermodynamic inhibitors are methanol, monoethylene glycol (MEG), and diethylene glycol (DEG), commonly referred to as glycol. All may be recovered and recirculated, but the economics of methanol recovery is not favourable in most cases. MEG is preferred over DEG for applications where the temperature is expected to be −10 °C or lower due to high viscosity at low temperatures. Triethylene glycol (TEG) has too low vapour pressure to be suited as an inhibitor injected into a gas stream. More methanol is lost in the gas phase when compared to MEG or DEG.

The use of kinetic inhibitors and anti-agglomerants in actual field operations is a new and evolving technology. It requires extensive tests and optimisation to the actual system. While kinetic inhibitors work by slowing down the kinetics of the nucleation, anti-agglomerants do not stop the nucleation, but stop the agglomeration (sticking together) of gas hydrate crystals. These two kinds of inhibitors are also known as low dosage hydrate inhibitors, because they require much smaller concentrations than the conventional thermodynamic inhibitors. Kinetic inhibitors, which do not require water and hydrocarbon mixture to be effective, are usually polymers or copolymers and anti-agglomerants (requires water and hydrocarbon mixture) are polymers or zwitterionic – usually ammonium and COOH – surfactants being both attracted to hydrates and hydrocarbons.

Empty clathrate hydrates

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Empty clathrate hydrates[30] are thermodynamically unstable (guest molecules are of paramount importance to stabilize these structures) with respect to ice, and as such their study using experimental techniques is greatly limited to very specific formation conditions; however, their mechanical stability renders theoretical and computer simulation methods the ideal choice to address their thermodynamic properties. Starting from very cold samples (110–145 K), Falenty et al.[31] degassed Ne–sII clathrates for several hours using vacuum pumping to obtain a so-called ice XVI, while employing neutron diffraction to observe that (i) the empty sII hydrate structure decomposes at T ≥ 145 K and, furthermore, (ii) the empty hydrate shows a negative thermal expansion at T < 55 K, and it is mechanically more stable and has a larger lattice constant at low temperatures than the Ne-filled analogue. The existence of such a porous ice had been theoretically predicted before.[32] From a theoretical perspective, empty hydrates can be probed using Molecular Dynamics or Monte Carlo techniques. Conde et al. used empty hydrates and a fully atomic description of the solid lattice to estimate the phase diagram of H2O at negative pressures and T ≤ 300 K,[33] and obtain the differences in chemical potentials between ice Ih and the empty hydrates, central to the van der Waals−Platteeuw theory. Jacobson et al. performed[34] simulations using a monoatomic (coarse-grained) model developed for H2O that is capable of capturing the tetrahedral symmetry of hydrates. Their calculations revealed that, under 1 atm pressure, sI and sII empty hydrates are metastable regarding the ice phases up to their melting temperatures, T = 245 ± 2 K and T = 252 ± 2 K, respectively. Matsui et al. employed[35] molecular dynamics to perform a thorough and systematic study of several ice polymorphs, namely space fullerene ices, zeolitic ices, and aeroices, and interpreted their relative stability in terms of geometrical considerations.

The thermodynamics of metastable empty sI clathrate hydrates have been probed over broad temperature and pressure ranges, 100 K ≤ T ≤ 220 K and 100 kPa ≤ p ≤ 500 MPa, by Cruz et al.[36] using large-scale simulations and compared with experimental data at 100 kPa. The whole p–V–T surface obtained was fitted by the universal form of the Parsafar and Mason equation of state with an accuracy of 99.7–99.9%. Framework deformation caused by applied temperature followed a parabolic law, and there is a critical temperature above which the isobaric thermal expansion becomes negative, ranging from 194.7 K at 100 kPa to 166.2 K at 500 MPa. Response to the applied (p, T) field was analyzed in terms of angle and distance descriptors of a classical tetrahedral structure and observed to occur essentially by means of angular alteration for (p, T) > (200 MPa, 200 K). The length of the hydrogen bonds responsible for framework integrity was insensitive to the thermodynamic conditions and its average value is r(̅O H) = 0.25 nm.

CO2 hydrate

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Clathrate hydrate, which encaged CO2 as guest molecule is termed as CO2 hydrate. The term CO2 hydrates are more commonly used these days with its relevance in anthropogenic CO2 capture and sequestration. A nonstoichiometric compound, carbon dioxide hydrate, is composed of hydrogen-bonded water molecules arranged in ice-like frameworks that are occupied by molecules with appropriate sizes and regions. In structure I, the CO2 hydrate crystallizes as one of two cubic hydrates composed of 46 H2O molecules (or D2O) and eight CO2 molecules occupying both large cavities (tetrakaidecahedral) and small cavities (pentagonal dodecahedral).[37] Researchers believed that oceans and permafrost have immense potential to capture anthropogenic CO2 in the form CO2 hydrates. The utilization of additives to shift the CO2 hydrate equilibrium curve in phase diagram towards higher temperature and lower pressures is still under scrutiny to make extensive large-scale storage of CO2 viable in shallower subsea depths.[38]

See also

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References

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  1. ^ Englezos, Peter (1993). "Clathrate hydrates". Industrial & Engineering Chemistry Research. 32 (7): 1251–1274. doi:10.1021/ie00019a001.
  2. ^ Hassanpouryouzband, Aliakbar; Joonaki, Edris; Vasheghani Farahani, Mehrdad; Takeya, Satoshi; Ruppel, Carolyn; Yang, Jinhai; J. English, Niall; M. Schicks, Judith; Edlmann, Katriona; Mehrabian, Hadi; M. Aman, Zachary; Tohidi, Bahman (2020). "Gas hydrates in sustainable chemistry". Chemical Society Reviews. 49 (15): 5225–5309. Bibcode:2020CSRev..49.5225H. doi:10.1039/C8CS00989A. hdl:1912/26136. PMID 32567615. S2CID 219971360.
  3. ^ Gao S; House W; Chapman WG (2005). "NMR MRI Study of Gas Hydrate Mechanisms". The Journal of Physical Chemistry B. 109 (41): 19090–19093. CiteSeerX 10.1.1.175.9193. doi:10.1021/jp052071w. PMID 16853461. S2CID 18762205. Retrieved August 3, 2009.
  4. ^ Gao S; Chapman WG; House W (2005). "NMR and Viscosity Investigation of Clathrate Formation and Dissociation". Ind. Eng. Chem. Res. 44 (19): 7373–7379. doi:10.1021/ie050464b. Retrieved August 3, 2009.
  5. ^ Choudhary, Nilesh; Chakrabarty, Suman; Roy, Sudip; Kumar, Rajnish (January 2019). "A comparison of different water models for melting point calculation of methane hydrate using molecular dynamics simulations". Chemical Physics. 516: 6–14. Bibcode:2019CP....516....6C. doi:10.1016/j.chemphys.2018.08.036. S2CID 106222519.
  6. ^ Michael Faraday (1859). On Hydrate of Chlorine. Quarterly Journal of Science. pp. 81–84. Retrieved 8 April 2024.
  7. ^ Ellen Thomas (November 2004). "Clathrates: little known components of the global carbon cycle". Wesleyan University. Retrieved 13 December 2007.
  8. ^ Buffett, B.; Archer, D. (2004). "Global inventory of methane clathrate: sensitivity to changes in the deep ocean". Earth Planet. Sci. Lett. 227 (3–4): 185–199. Bibcode:2004E&PSL.227..185B. doi:10.1016/j.epsl.2004.09.005.
  9. ^ Chong, Zheng Rong; Yang, She Hern Bryan; Babu, Ponnivalavan; Linga, Praveen; Li, Xiao-Sen (2016). "Review of natural gas hydrates as an energy resource: Prospects and challenges". Applied Energy. 162: 1633–1652. Bibcode:2016ApEn..162.1633C. doi:10.1016/j.apenergy.2014.12.061.
  10. ^ "Drinkable water from cold energy | Engineers Australia".
  11. ^ "Eco-friendly ways to harness natural gas efficiently". The Straits Times. 30 June 2017.
  12. ^ Babu, Ponnivalavan; Linga, Praveen; Kumar, Rajnish; Englezos, Peter (1 June 2015). "A review of the hydrate based gas separation (HBGS) process for carbon dioxide pre-combustion capture". Energy. 85: 261–279. Bibcode:2015Ene....85..261B. doi:10.1016/j.energy.2015.03.103.
  13. ^ "NUS, Keppel, SLNG in tie-up to develop better cooling technology for data centres". The Straits Times. 22 October 2019.
  14. ^ Ghosh, Jyotirmoy; Methikkalam, Rabin Rajan J.; Bhuin, Radha Gobinda; Ragupathy, Gopi; Choudhary, Nilesh; Kumar, Rajnish; Pradeep, Thalappil (29 January 2019). "Clathrate hydrates in interstellar environment". Proceedings of the National Academy of Sciences. 116 (5): 1526–1531. Bibcode:2019PNAS..116.1526G. doi:10.1073/pnas.1814293116. PMC 6358667. PMID 30630945.
  15. ^ Thomas, Ellen (November 2004). "Clathrates: little known components of the global carbon cycle". Wesleyan University. Retrieved 13 December 2007.
  16. ^ Hammerschmidt, E. G. (1934-08-01). "Formation of Gas Hydrates in Natural Gas Transmission Lines". Industrial & Engineering Chemistry. 26 (8): 851–855. doi:10.1021/ie50296a010. ISSN 0019-7866.
  17. ^ a b Cite error: The named reference :0 was invoked but never defined (see the help page).
  18. ^ Latin dictionary Archived 2012-04-14 at the Wayback Machine
  19. ^ Stackelberg, M. v; Müller, H. R. (1954). "Feste Gashydrate II. Struktur und Raumchemie" [Solid gas hydrates II. Structure and space chemistry]. Zeitschrift für Elektrochemie, Berichte der Bunsengesellschaft für physikalische Chemie (in German). 58 (1): 25–39. doi:10.1002/bbpc.19540580105. S2CID 93862670.
  20. ^ Sloan, E. Dendy & Koh, Carolyn A. (2008) [1st pub. 1998]. "Chapter 2. Molecular Structures and Similarities to Ice". Clathrate hydrates of natural gases. CRC Press. p. 45. ISBN 978-0-8493-9078-4.
  21. ^ Birchall, T.; Frampton, C. S.; Schrobilgen, G. J.; Valsdóttir, J. (1989). "Β-Hydroquinone xenon clathrate". Acta Crystallographica Section C Crystal Structure Communications. 45 (6): 944–946. Bibcode:1989AcCrC..45..944B. doi:10.1107/S0108270188014556.
  22. ^ Kvenvolden, Keith A.; McMenamin, Mark A. (1980). "Hydrates of natural gas; a review of their geologic occurrence". Circular (Report). doi:10.3133/cir825.
  23. ^ Marshall, Michael (26 March 2009). "Ice that burns could be a green fossil fuel". New Scientist.
  24. ^ Ussler, W.; Paull, C. K.; Lorenson, T.; Dallimore, S.; Medioli, B.; Blasco, S.; McLaughlin, F.; Nixon, F. M. (2005). "Methane Leakage from Pingo-like Features on the Arctic Shelf, Beaufort Sea, NWT, Canada". AGU Fall Meeting Abstracts. 2005: C11A–1069. Bibcode:2005AGUFM.C11A1069U.
  25. ^ Youssef, Z.; Barreau, A.; Mougin, P.; Jose, J.; Mokbel, I. (15 April 2009). "Measurements of Hydrate Dissociation Temperature of Methane, Ethane, and CO2 in the Absence of Any Aqueous Phase and Prediction with the Cubic Plus Association Equation of State". Industrial & Engineering Chemistry Research. 48 (8): 4045–4050. doi:10.1021/ie801351e.
  26. ^ "China claims breakthrough in 'flammable ice'". BBC News. 19 May 2017.
  27. ^ "China and Japan find way to extract 'combustible ice' from seafloor, harnessing a legendary frozen fossil fuel". National Post. 19 May 2017.
  28. ^ "Web of Science".
  29. ^ Gao, Shuqiang (2008). "Investigation of Interactions between Gas Hydrates and Several Other Flow Assurance Elements". Energy & Fuels. 22 (5): 3150–3153. doi:10.1021/ef800189k.
  30. ^ Cruz, Fernando J. A. L.; Alavi, Saman; Mota, José P. B. (2019). "Low-Temperature Thermodynamic Study of the Metastable Empty Clathrate Hydrates Using Molecular Simulations". ACS Earth and Space Chemistry. 3 (5): 789–799. Bibcode:2019ESC.....3..789C. doi:10.1021/acsearthspacechem.9b00009. S2CID 140362440.
  31. ^ Falenty A.; Hansen T.C.; Kuhs F. (2014). "Formation and Properties of Ice XVI Obtained by Emptying a Type sII Clathrate Hydrate". Nature. 516 (7530): 231–234. Bibcode:2014Natur.516..231F. doi:10.1038/nature14014. PMID 25503235. S2CID 4464711.
  32. ^ Kosyakov V.I. (2009). "Structure Formation Under Negative Pressures". J. Struct. Chem. 50: 60–65. Bibcode:2009JStCh..50S..60K. doi:10.1007/s10947-009-0190-0. S2CID 97767359.
  33. ^ Conde M.M.; Vega C.; Tribello G.A.; Slater B. (2009). "The Phase Diagram of Water at Negative Pressures: Virtual Ices". J. Chem. Phys. 131 (3): 034510. Bibcode:2009JChPh.131c4510C. doi:10.1063/1.3182727. PMID 19624212.
  34. ^ Jacobson L.C.; Hujo W.; Molinero V. (2009). "Thermodynamic Stability and Growth of Guest-Free Clathrate Hydrates: A Low-Density Crystal Phase of Water". J. Phys. Chem. B. 113 (30): 10298–10307. doi:10.1021/jp903439a. PMID 19585976.
  35. ^ Matsui T.; Hirata M.; Yagasaki T.; Matsumoto M.; Tanaka H. (2017). "Hypothetical Ultralow-density Ice Polymorphs". J. Chem. Phys. 147 (9): 091101. doi:10.1063/1.4994757. PMID 28886658.
  36. ^ Cruz F.J.A.L.; Alavi S.; Mota J.P.B. (2019). "Low-Temperature Thermodynamic Study of the Metastable Empty Clathrate Hydrates Using Molecular Simulations". ACS Earth and Space Chemistry. 3 (5): 789–799. Bibcode:2019ESC.....3..789C. doi:10.1021/acsearthspacechem.9b00009. S2CID 140362440.
  37. ^ Circone S.; Stern L.A.; Kirby S.H.; Durham W.B.; Chacoumakos B.C.; Rawn C.J.; Rondinone A.J.; Ishii Y. (2003). "CO2 Hydrate: Synthesis, Composition, Structure, Dissociation Behavior, and a Comparison to Structure I CH4 Hydrate". The Journal of Physical Chemistry B. 107 (23): 5529–5539. Bibcode:2003JPCB..107.5529C. doi:10.1021/jp027391j.
  38. ^ Zheng J.; Chong Z.R.; Qureshi M.F.; Linga P. (2020). "Carbon Dioxide Sequestration via Gas Hydrates: A Potential Pathway toward Decarbonization". Energy Fuels. 34 (9): 10529–10546. doi:10.1021/acs.energyfuels.0c02309. S2CID 225428567.

Further reading

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