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Journal articles on the topic 'Ethane'

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Published: 4 June 2021
Last updated: 22 June 2024

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1

Quarles, Carroll, and Lee Estep. "Molecular-field bremsstrahlung in ethane, ethene and ethyne." Physics Letters A 114, no. 1 (January 1986): 9–12. http://dx.doi.org/10.1016/0375-9601(86)90331-2.

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2

Rüdinger, Christoph, Holger Beruda, and Hubert Schmidbaur. "Synthesis and Molecular Structure of Silylated Ethenes and Acetylenes." Zeitschrift für Naturforschung B 49, no. 10 (October 1, 1994): 1348–60. http://dx.doi.org/10.1515/znb-1994-1008.

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AbstractDisilylacetylene (1) has been obtained from LiAlH4 reduction of bis(trichlorosilyl)acetylene (2) and bis[(trifluoromethylsulfonyloxy)silyl]acetylene (4). The catalytic hydrosilylation of 2 with HSiCl3 affords tris(trichlorosilyl)ethene (5) and 1.1.2-tris(trichlorosilyl)ethane (6). The synthesis of 6, trans-bis(trichlorosilyl)ethene (8) and 1,1-bis(trichlorosilyl)ethene (9) has been accomplished by hydrosilyiation of trichlorosilylacetylene (7) which was synthesized by the reaction of trichloro(trifluoromethylsulfonyloxy)silane with sodium acetylide. Reductive elimination of halogen from 1,1,1,2-tetrachloro-bis(trichlorosilyl)ethane (10) and 1,2- dibromo-1,1-bis(trichlorosiIyl)ethane (13) gave the corresponding ethenes 1,1-dichloro-bis- (trichlorosilyl)ethene (11), trichloro-trichlorosilylethene (12), 1,1-bis(trichlorosilyl)ethene (9) and 1-chloro-2,2-bis(trichlorosilyl)ethene (14). Tetrakis(trichlorosilyl)ethene (15) has been obtained in a three step synthesis starting from chloromethyl-trichlorosilane or dichloro- methyl-trichlorosilane. By LiAlH4 reduction of trichlorosilylethenes under various reaction conditions, the silylethenes trans-dichloro-di(silyl)ethene (16), 1,1-dichloro-di(silyl)ethene (17), trichloro-silylethene (18), 1-bromo-l-silylethene (19), trans-di(silyl)ethene (20), 1-chloro-2,2-di(silyl)ethene (21), tri(silyl)ethene (22) and 1,1,2-tri(silyl)ethane (23) could be generated. Silylethyne and silyl-chloroethyne were identified as side products. The crystal and molecular structures of 2,5 and 15 have been determined by single crystal X-ray diffraction. 2 and 5 crystallize from the melt in the monoclinic space groups Cc and P21/n, respectively. 15 has been crystallized by sublimation (orthorhombic. space group Pbca). 5 and 15 feature strongly distorted ethene skeletons with a double bond twist of 28.1° in 15.
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3

Timár, Máté, Gergely Barcza, Florian Gebhard, Libor Veis, and Örs Legeza. "Hückel–Hubbard–Ohno modeling of π-bonds in ethene and ethyne with application to trans-polyacetylene." Physical Chemistry Chemical Physics 18, no. 28 (2016): 18835–45. http://dx.doi.org/10.1039/c6cp00726k.

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Quantum chemistry calculations provide the potential energy between two carbon atoms in ethane (H3C–CH3), ethene (H2CCH2), and ethyne (HCCH) as a function of the atomic distance.
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4

Lee, Christopher J., Marcus A. Sharp, R. Scott Smith, Bruce D. Kay, and Zdenek Dohnálek. "Adsorption of ethane, ethene, and ethyne on reconstructed Fe3O4(001)." Surface Science 714 (December 2021): 121932. http://dx.doi.org/10.1016/j.susc.2021.121932.

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5

Oh, So Hyeon, In Yeub Hwang, Ok Kyung Lee, Wangyun Won, and Eun Yeol Lee. "Development and Optimization of the Biological Conversion of Ethane to Ethanol Using Whole-Cell Methanotrophs Possessing Methane Monooxygenase." Molecules 24, no. 3 (February 7, 2019): 591. http://dx.doi.org/10.3390/molecules24030591.

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The biological production of ethanol from ethane for the utilization of ethane in natural gas was investigated under ambient conditions using whole-cell methanotrophs possessing methane monooxygenase. Several independent variables including ethane concentration and biocatalyst amounts, among other factors, were optimized for the enhancement of ethane-to-ethanol bioconversion. We obtained 0.4 g/L/h of volumetric productivity and 0.52 g/L of maximum titer in optimum batch reaction conditions. In this study, we demonstrate that the biological gas-to-liquid conversion of ethane to ethanol has potent technical feasibility as a new application of ethane gas.
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6

Herjavić, Glenda, Brunislav Matasović, Gregor Arh, and Elvira Kovač-Andrić. "Investigation of Non-Methane Hydrocarbons at a Central Adriatic Marine Site Mali Lošinj, Croatia." Atmosphere 11, no. 6 (June 18, 2020): 651. http://dx.doi.org/10.3390/atmos11060651.

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For the first time, volatile hydrocarbons were measured in Croatia, at Mali Lošinj in the period from autumn 2004 to autumn 2005. Mali Lošinj site is conveniently located as a gateway to Croatia for any potential pollution from either Po valley in Italy, or other locations in southern Europe or even Africa. The sampling was performed on multisorbent tubes and then analyzed by thermal desorption gas chromatography with a flame ionization detector. The aim was to determine and estimate the non-methane hydrocarbons in Mali Lošinj, a location with Mediterranean vegetation and species which emit large quantities of volatile organic compounds. Ozone volume fraction and meteorological parameters were also continuously measured, from April to October 2005. Ethane, ethene, ethyne, propane, propene, n-pentane, n-hexane, benzene and toluene were identified in all air samples. Benzene and toluene have been found in ambient air and significant positive correlations between ethyne and ethane, propane and propene indicate emissions from transport.
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7

Werstiuk, N. H. "Thermolysis of N-alkylated ethylenediamines: an ultraviolet photoelectron spectroscopy study." Canadian Journal of Chemistry 64, no. 11 (November 1, 1986): 2175–83. http://dx.doi.org/10.1139/v86-358.

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Thermolyses of N,N,N′,N′-tetramethylethylenediamine (1a), N,N,N′,N′-tetraethylethylenediamine (1b) and sym-N,N′-dimethylethylenediamine (1c) at 760–825 °C have been studied by ultraviolet photoelectron spectroscopy. Although the corresponding N-alkylated aminomethylene radicals were not observed, this study establishes that thermolysis of 1a is an efficient route to N-methylenimine (3a); methane, ethane, and ethene are the other major products. Diamine 1b yields, besides ethane, ethene, and propane, heretofore unreported N-ethylmethylenimine (3b). Diamine 1c yields imine 3a and methylenimine (3c), as well as hydrogen, methane, ethane, and ethene. Molecular orbital eigenvalues of the imines are calculated using HAM/3, MNDO, HF/STO-3G, HF/3-21G, and HF/6-31G* methods.
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8

Aristov, N., and Peter B. Armentrout. "Reaction mechanisms and thermochemistry of vanadium ions with ethane, ethene and ethyne." Journal of the American Chemical Society 108, no. 8 (April 1986): 1806–19. http://dx.doi.org/10.1021/ja00268a017.

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9

Schmidbaur, Hubert, Christos Paschalidis, Gabriele Reber, and Gerhard Müller. "Ambidente Poly(diphenylphosphino)ethane und -ethene." Chemische Berichte 121, no. 7 (July 1988): 1241–45. http://dx.doi.org/10.1002/cber.19881210706.

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10

Martin, Heinz, and Helmut Bretinger. "Bis- und Tris(aluminium)alkan-Verbindungen, II: 1,1- und 1,2-Bis(chloro/ethylaluminium)ethan / Bis- and Tris(aluminum)alkane Compounds, II: 1,1- and 1,2-Bis(chloro/ethylaluminum)ethanes." Zeitschrift für Naturforschung B 46, no. 5 (May 1, 1991): 615–20. http://dx.doi.org/10.1515/znb-1991-0509.

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The syntheses of bis(aluminum)ethane compounds – bis(dichloroaluminum)ethanes to chlorine free bis(diethylaluminum)ethanes 1-10 are described. The connecting ethylene between the two aluminum atoms is identified either as C2H4 (1,2–) or as CH(CH3) (1,1–). The syntheses of Cl2AlEt, ethylaluminumsesquichloride and Et2AlCl from aluminum, ethylene and AlCl3 or EtAlCl2 via bis(aluminum)ethane compounds under various conditions are presented.
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11

Anderson, Jeffrey A. "Production of Methanol from Heat-stressed Pepper and Corn Leaf Disks." Journal of the American Society for Horticultural Science 119, no. 3 (May 1994): 468–72. http://dx.doi.org/10.21273/jashs.119.3.468.

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`Early Calwonder' pepper (Capsicum annuum L.) and `Jubilee' corn (Zea mays L.) leaf disks exposed to high temperature stress produced ethylene, ethane, methanol, acetaldehyde, and ethanol based on comparison of retention times during gas chromatography to authentic standards. Methanol, ethanol, and acetaldehyde were also identified by mass spectroscopy. Corn leaf disks produced lower levels of ethylene, ethane, and methanol, but more acetaldehyde and ethanol than pepper. Production of ethane, a by-product of lipid peroxidation, coincided with an increase in electrolyte leakage (EL) in pepper but not in corn. Compared with controls, pepper leaf disks infiltrated with linolenic acid evolved significantly greater amounts of ethane, acetaldehyde, and methanol and similar levels of ethanol. EL and volatile hydrocarbon production were not affected by fatty acid infiltration in corn. Infiltration of pepper leaves with buffers increasing in pH from 5.5 to 9.5 increased methanol production.
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12

Anderson, Jeffrey A. "METHANOL PRODUCTION FROM HEAT-STRESSED PEPPER AND CORN LEAF DISKS." HortScience 28, no. 5 (May 1993): 587a—587. http://dx.doi.org/10.21273/hortsci.28.5.587a.

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Pepper (Capsicum annuum L. `Early Calwonder') and corn (Zea mays L. `Jubilee') leaf disks exposed to high temperature stress produced ethylene, ethane, methanol, acetaldehyde, and ethanol based on comparison of retention times during gas chromatography to authentic standards. Methanol, ethanol, and acetaldehyde were also identified by mass spectroscopy. Corn leaf disks produced lower levels of ethylene, ethane and methanol, but more acetaldehyde and ethanol than pepper. Production of ethane, a by-product of lipid peroxidation, coincided with an increase in electrolyte leakage (EL) in pepper but not in corn. Compared with controls, pepper leaf disks infiltrated with linolenic acid evolved significantly greater amounts of ethane, acetaldehyde and methanol, and similar levels of ethanol. Introduction of linoleic acid did not significantly affect volatile hydrocarbon production in pepper. Electrolyte leakage and volatile hydrocarbon production were not affected by fatty acid infiltration in corn.
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13

Schoellner, R., and U. Mueller. "Influence of Mono- and Bivalent Cations in 4A-Zeolites on the Adsorptive Separation of Ethene and Propene from Crack-Gases." Adsorption Science & Technology 3, no. 3 (September 1986): 167–71. http://dx.doi.org/10.1177/026361748600300306.

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Adsorption of ethane/ethene, propane/propene and methane, ethane/ethene, propene mixtures was examined on 4A-zeolites K0·08Na0·92A, Ba0·2Na0·8A, Mg0·2Na0·8A and NaA by measurement of breakthrough curves. Separation of the alkenes and alkanes, especially dynamic capacities, the purity of the desorbates and yields of olefins, confirm the accepted transport mechanism of small alkenes in 4A-zeolites. It is possible to vary the blocking cations and the adsorption centres in the large cavities to obtain favourable conditions for a common separation of ethene and propene from crack-gases.
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14

Altintas, Cigdem, and Seda Keskin. "Molecular simulations of MOF membranes for separation of ethane/ethene and ethane/methane mixtures." RSC Advances 7, no. 82 (2017): 52283–95. http://dx.doi.org/10.1039/c7ra11562h.

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Molecular simulations were used to assess the membrane-based C2H6/C2H4 and C2H6/CH4 separation performances of 175 different MOF structures.
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15

He, Xuefeng, Zhe Li, Huihui Hu, Jiawei Chen, Lingzhen Zeng, Jingzheng Zhang, Wenbin Lin, and Cheng Wang. "Chemical looping conversion of ethane to ethanol via photo-assisted nitration of ethane." Cell Reports Physical Science 2, no. 7 (July 2021): 100481. http://dx.doi.org/10.1016/j.xcrp.2021.100481.

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16

Casado, Martin, Michael J. Freedman, Justin Pettit, Jianying Luo, Nick McKeown, and Scott Shenker. "Ethane." ACM SIGCOMM Computer Communication Review 37, no. 4 (October 2007): 1–12. http://dx.doi.org/10.1145/1282427.1282382.

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17

Garbacz, J. K., and M. Dabrowski. "A Non-Analytical Solution of the Description of Single Gas Adsorption on a Microporous Adsorbent." Adsorption Science & Technology 15, no. 2 (January 1997): 99–108. http://dx.doi.org/10.1177/026361749701500203.

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Two distribution functions for the energy of localization dividing two neighbouring adsorption sites were suggested for the model of partially mobile adsorption on energetically heterogeneous microporous solids. The experimental isotherms of ethane adsorption on NaX-type zeolite derivatives cationized by Li+, K+, Rb+, Ca2+, Sr2+ ions as well as isotherms of ethane, ethene and n-pentane adsorption on NaX-type zeolite were described by the relationships of the proposed adsorption model.
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18

Nami, Navabeh, Mehdi Forozani, Vida Khosravimoghadam, and Rahmatallah Taherinasab. "Synthesis and Characterization of Mono- and Bicycle Heterocyclic Derivatives Containing 1, 2,4-Triazole, 1,3,4-Thiadiazine and 1,3-Thiazole Rings." E-Journal of Chemistry 9, no. 1 (2012): 161–66. http://dx.doi.org/10.1155/2012/867637.

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Reaction of tartaric acid with thiocarbohydrazide(2)and thiosemicarbazide(6)afforded 1,2-bis(4-amino-5-mercapto-4H-1,2,4-triazol-3-yl)-ethane-1,2-diol(3)and 1,2-bis(5-mercapto-4H-1,2,4-triazol-3-yl)-ethane-1,2-diol(7). Reaction of compounds3and7with DMAD (dimethylacety lendi carboxylate) and DEAD (diethylacetylendicarboxylate) gave 1,2-bis(7-[(z)-methoxycarbonylmethylen]-5,6-dihydro-5H-6-one-[1,2,4] riazolo[3,4-b] [1,3,4] thiadiazin-3-yl)-ethan-1,2-diol(4), 1,2-bis(7-[(z)-ethoxycarbonylmethylen] -5,6-dihydro -5H-6-one-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-3-yl)-ethan-1,2- diol(5)and 1,2-bis(6-[(z)-methoxycarbonylmethylen]-5-oxo-[1,3]thiazolo[2,3-c] [1,2,4]triazol-3-yl)-ethan-1,2-diol(8)in good yields.
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19

Melzer, Daniel, Gerhard Mestl, Klaus Wanninger, Andreas Jentys, Maricruz Sanchez-Sanchez, and Johannes A. Lercher. "On the Promoting Effects of Te and Nb in the Activity and Selectivity of M1 MoV-Oxides for Ethane Oxidative Dehydrogenation." Topics in Catalysis 63, no. 19-20 (July 8, 2020): 1754–64. http://dx.doi.org/10.1007/s11244-020-01304-0.

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AbstractThe pathways of ethane oxidative dehydrogenation and total combustion have been elucidated for M1 phase type Mo–V oxide catalysts with different metal composition. The ethane oxidation mechanism is not affected by the presence of Te or Nb. Conversely, the selectivity is strongly affected by stoichiometry of M1 catalysts. This is attributed to the facile oxidation of ethene to COx upon formation of unselective VOx species in the absence of Te and Nb.
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20

Wilson, C., A. S. O'Neil, A. J. Blake, M. Poliakoff, A. E. Goeta, and J. A. K. Howard. "New intercalation compounds of C60with ethene and ethane." Acta Crystallographica Section A Foundations of Crystallography 58, s1 (August 6, 2002): c129. http://dx.doi.org/10.1107/s0108767302090177.

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21

Tumba, Kaniki, Paramespri Naidoo, Amir H. Mohammadi, Dominique Richon, and Deresh Ramjugernath. "Phase Equilibria of Clathrate Hydrates of Ethane + Ethene." Journal of Chemical & Engineering Data 58, no. 4 (March 27, 2013): 896–901. http://dx.doi.org/10.1021/je301051c.

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22

González Abad, G., N. D. C. Allen, P. F. Bernath, C. D. Boone, S. D. McLeod, G. L. Manney, G. C. Toon, et al. "Ethane, ethyne and carbon monoxide concentrations in the upper troposphere and lower stratosphere from ACE and GEOS-Chem: a comparison study." Atmospheric Chemistry and Physics Discussions 11, no. 4 (April 28, 2011): 13099–139. http://dx.doi.org/10.5194/acpd-11-13099-2011.

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Abstract. Near global upper tropospheric concentrations of carbon monoxide (CO), ethane (C2H6) and ethyne (C2H2) from ACE (Atmospheric Chemistry Experiment) Fourier transform spectrometer on board the Canadian satellite SCISAT-1 are presented and compared with the output from the Chemical Transport Model (CTM) GEOS-Chem. The retrievals of ethane and ethyne from ACE have been improved for this paper by using new sets of microwindows compared with those for previous versions of ACE data. With the improved ethyne retrieval we have been able to produce a near global upper tropospheric distribution of C2H2 from space. Carbon monoxide, ethane and ethyne concentrations retrieved using ACE spectra show the expected seasonality linked to variations in the anthropogenic emissions and destruction rates as well as seasonal biomass burning activity. The GEOS-Chem model was run using the dicarbonyl chemistry suite, an extended chemical mechanism in which ethyne is treated explicitly. Seasonal cycles observed from satellite data are well reproduced by the model output, however the simulated CO concentrations are found to be systematically biased low over the Northern Hemisphere. An average negative global mean bias of 12% and 7% of the model relative to the satellite observations has been found for CO and C2H6 respectively and a positive global mean bias of 1% has been found for C2H2. ACE data are compared for validation purposes with MkIV spectrometer data and Global Tropospheric Experiment (GTE) TRACE-A campaign data showing good agreement with all of them.
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23

González Abad, G., N. D. C. Allen, P. F. Bernath, C. D. Boone, S. D. McLeod, G. L. Manney, G. C. Toon, et al. "Ethane, ethyne and carbon monoxide concentrations in the upper troposphere and lower stratosphere from ACE and GEOS-Chem: a comparison study." Atmospheric Chemistry and Physics 11, no. 18 (September 27, 2011): 9927–41. http://dx.doi.org/10.5194/acp-11-9927-2011.

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Abstract. Near global upper tropospheric concentrations of carbon monoxide (CO), ethane (C2H6) and ethyne (C2H2) from ACE (Atmospheric Chemistry Experiment) Fourier transform spectrometer on board the Canadian satellite SCISAT-1 are presented and compared with the output from the Chemical Transport Model (CTM) GEOS-Chem. The retrievals of ethane and ethyne from ACE have been improved for this paper by using new sets of microwindows compared with those for previous versions of ACE data. With the improved ethyne retrieval we have been able to produce a near global upper tropospheric distribution of C2H2 from space. Carbon monoxide, ethane and ethyne concentrations retrieved using ACE spectra show the expected seasonality linked to variations in the anthropogenic emissions and destruction rates as well as seasonal biomass burning activity. The GEOS-Chem model was run using the dicarbonyl chemistry suite, an extended chemical mechanism in which ethyne is treated explicitly. Seasonal cycles observed from satellite data are well reproduced by the model output, however the simulated CO concentrations are found to be systematically biased low over the Northern Hemisphere. An average negative global mean bias of 12% and 7% of the model relative to the satellite observations has been found for CO and C2H6 respectively and a positive global mean bias of 1% has been found for C2H2. ACE data are compared for validation purposes with MkIV spectrometer data and Global Tropospheric Experiment (GTE) TRACE-A campaign data showing good agreement with all of them.
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24

Yang, Huajun, Yanxiang Wang, Rajamani Krishna, Xiaoxia Jia, Yong Wang, Anh N. Hong, Candy Dang, Henry E. Castillo, Xianhui Bu, and Pingyun Feng. "Pore-Space-Partition-Enabled Exceptional Ethane Uptake and Ethane-Selective Ethane–Ethylene Separation." Journal of the American Chemical Society 142, no. 5 (January 27, 2020): 2222–27. http://dx.doi.org/10.1021/jacs.9b12924.

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25

McElroy, Peter J., and Ji Fang. "Compression factors and virial coefficients of ethene and ethene + ethane mixtures." Journal of Chemical & Engineering Data 38, no. 3 (July 1993): 410–13. http://dx.doi.org/10.1021/je00011a021.

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26

Čapek, Libor, Lukáš Vaněk, Lucie Smoláková, Roman Bulánek, and Jiří Adam. "The Feasibility of Ni-Alumina Catalysts in Oxidative Dehydrogenation of Ethane." Collection of Czechoslovak Chemical Communications 73, no. 8-9 (2008): 1177–91. http://dx.doi.org/10.1135/cccc20081177.

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The contribution deals with the development on the efficient Ni-alumina catalyst for the oxidative dehydrogenation (ODH) of ethane to ethene. The performance of Ni-alumina catalysts with varying nickel loadings and with thermal pretreatment was studied. We contribute to the understanding of the relationship between the activity of nickel species in ODH of ethane and its distribution. To analyze this effect, Ni-alumina catalysts were analyzed by UV-VIS spectroscopy, and H2-TPR profile. Ni-alumina catalysts were highly active and selective (ca. 80%) in the ODH of ethane. The catalysts contained both tetrahedral and octahedral nickel species, suggesting that nickel aluminate represented a partial spinel, where Ni(II) ions occupy both octahedral and tetrahedral sites of the oxygen lattice. It was suggested that the octahedral nickel species were more active than the tetrahedral ones.
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27

Khan, Firoz Shah Tuglak, Syed Jehanger Shah, Susovan Bhowmik, Fabián G. Cantú Reinhard, Mala A. Sainna, Sam P. de Visser, and Sankar Prasad Rath. "Equatorial ligand plane perturbations lead to a spin-state change in an iron(iii) porphyrin dimer." Dalton Transactions 48, no. 19 (2019): 6353–57. http://dx.doi.org/10.1039/c9dt01182j.

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28

Najari, Sara, Samrand Saeidi, Patricia Concepcion, Dionysios D. Dionysiou, Suresh K. Bhargava, Adam F. Lee, and Karen Wilson. "Oxidative dehydrogenation of ethane: catalytic and mechanistic aspects and future trends." Chemical Society Reviews 50, no. 7 (2021): 4564–605. http://dx.doi.org/10.1039/d0cs01518k.

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Ethane oxidative dehydrogenation (ODH) is an attractive, low energy, alternative route to reduce the carbon footprint for ethene production, however, the commercial implementation of ODH processes requires catalysts with improved selectivity.
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29

Mondal, Suvendu Sekhar, Maximilian Hovestadt, Subarna Dey, Carolin Paula, Sebastian Glomb, Alexandra Kelling, Uwe Schilde, Christoph Janiak, Martin Hartmann, and Hans-Jürgen Holdt. "Synthesis of a partially fluorinated ZIF-8 analog for ethane/ethene separation." CrystEngComm 19, no. 39 (2017): 5882–91. http://dx.doi.org/10.1039/c7ce01438d.

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30

Heffernan, Olive. "Assessing ethane." Nature Climate Change 1, no. 812 (November 20, 2008): 152. http://dx.doi.org/10.1038/climate.2008.124.

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31

Kanoh, Soichiro, Hideo Kobayashi, and Kazuo Motoyoshi. "Exhaled Ethane." Chest 128, no. 4 (October 2005): 2387–92. http://dx.doi.org/10.1378/chest.128.4.2387.

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32

Choudhary, Vasant R., and Amarjeet M. Rajput. "Oscillations in homogeneous oxidative dehydrogenation of ethane to ethene." Journal of the Chemical Society, Faraday Transactions 91, no. 5 (1995): 843. http://dx.doi.org/10.1039/ft9959100843.

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33

Mapstone, B., M. J. Brunger, and W. R. Newell. "Vibrational excitation of ethane and ethene by electron impact." Journal of Physics B: Atomic, Molecular and Optical Physics 33, no. 1 (December 13, 1999): 23–35. http://dx.doi.org/10.1088/0953-4075/33/1/303.

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34

Akita, Munetaka, Shuichiro Sugimoto, Masako Tanaka, and Yoshihiko Morooka. "Preparation, characterization, and sequential transformation of dicarbide cluster compounds with permetalated ethyne, ethene, and ethane structures." Journal of the American Chemical Society 114, no. 19 (September 1992): 7581–82. http://dx.doi.org/10.1021/ja00045a051.

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35

Fung, Victor, Franklin (Feng) Tao, and De-en Jiang. "Understanding oxidative dehydrogenation of ethane on Co3O4 nanorods from density functional theory." Catalysis Science & Technology 6, no. 18 (2016): 6861–69. http://dx.doi.org/10.1039/c6cy00749j.

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Density functional theory calculations reveal the complete pathways of oxidative dehydrogenation of ethane to form ethene on the Co3O4(111) surface and the rate-determining step.
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36

Ishikawa, Satoshi, and Wataru Ueda. "Microporous crystalline Mo–V mixed oxides for selective oxidations." Catalysis Science & Technology 6, no. 3 (2016): 617–29. http://dx.doi.org/10.1039/c5cy01435b.

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Recent developments of crystalline Mo3VOx catalysts (MoVO), a new type of oxidation catalysts for selective oxidations of ethane to ethene and of acrolein to acrylic acid, are reviewed.
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37

Shimoda, Masahiro, Mitsufumi Ono, and Ichiro Okura. "Ethanol formation from ethane with Methylosinus trichosporium (OB3b)." Journal of Molecular Catalysis 52, no. 3 (July 1989): L37—L39. http://dx.doi.org/10.1016/0304-5102(89)85038-2.

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38

KAMINISHI, Gen-ichi, Chiaki YOKOYAMA, and Shinji TAKAHASHI. "Vapor pressures of n-butane-ethane, isobutane-ethane, and n-butane-isobutane-propane-ethane systems." Journal of The Japan Petroleum Institute 29, no. 1 (1986): 32–37. http://dx.doi.org/10.1627/jpi1958.29.32.

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39

Honda, Yusuke, Naoya Fujiwara, Shohei Tada, Yasukazu Kobayashi, Shigeo Ted Oyama, and Ryuji Kikuchi. "Direct electrochemical synthesis of oxygenates from ethane using phosphate-based electrolysis cells." Chemical Communications 56, no. 76 (2020): 11199–202. http://dx.doi.org/10.1039/d0cc05111j.

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40

Torres-García, G., D. P. Luis, G. Odriozola, and J. López-Lemus. "Ethane clathrates using different water–ethane models: Molecular dynamics." Physica A: Statistical Mechanics and its Applications 491 (February 2018): 89–100. http://dx.doi.org/10.1016/j.physa.2017.09.016.

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41

Decleva, Piero, Daniele Toffoli, Rajesh Kumar Kushawaha, Michael MacDonald, Maria Novella Piancastelli, Marc Simon, and Lucia Zuin. "Interference effects in photoelectron asymmetry parameter (β) trends of C 2s−1states of ethyne, ethene and ethane." Journal of Physics B: Atomic, Molecular and Optical Physics 49, no. 23 (November 18, 2016): 235102. http://dx.doi.org/10.1088/0953-4075/49/23/235102.

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42

Markova, Velina K., Georgi N. Vayssilov, Alexander Genest, and Notker Rösch. "Adsorption and transformations of ethene on hydrogenated rhodium clusters in faujasite-type zeolite. A computational study." Catalysis Science & Technology 6, no. 6 (2016): 1726–36. http://dx.doi.org/10.1039/c5cy01589h.

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Phase diagrams from DFT modeling suggest that zeolite-supported Rh4 clusters may be appropriate for the catalytic hydrogenation of ethene to ethane, whereas Rh3 clusters favor the formation of the stable adsorbed ethylidyne species, preventing further hydrogenation.
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43

Ban, Jiuqing, Changjun Li, Wei Yang, Wei Zhang, Xiaoyun Yuan, and Yingying Xu. "Prediction of Physical Properties and Phase Characteristics of Ethane and Ethane Mixture in the Ethane Pipeline." Processes 11, no. 8 (July 29, 2023): 2283. http://dx.doi.org/10.3390/pr11082283.

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In order to realize the safe transportation of liquefied ethane pipeline in the Oilfield of China, it is necessary to fully study the process of pipeline replacement, operation and shutdown. The accurate calculation of physical property parameters and critical parameters is the basis of studying the gas-liquid two-phase flow and heat and mass transfer process of liquefied ethane in the pipeline. In this paper, different equations of states (EOSs) were used to predict the physical properties (such as density, dew point and dynamic viscosity) of ethane or ethane mixture, and the predicted results were compared with the corresponding experimental data from the literature. The prediction performance of different EOSs were evaluated by using two evaluation indicators, including average absolute deviation (AAD) and average relative deviation (ARD). The results showed that the PR-Peneloux EOS has the best performance for predicting the density of CH4-C2H6-N2 mixture with an ARD value of 4.46%; for predicting the dew point, the BWRS EOS exhibits the superior performance with an ARD value of 0.58%; and for predicting dynamic viscosity, the SuperTRAPP formula has the smallest calculation error, with an ARD value of 1.33%. Considering the comparison results of the calculation accuracy of density, dew point and dynamic viscosity of ethane or ethane mixture by using different EOSs, PR-Peneloux EOS was recommended to calculate the phase characteristics in the process of ethane pipeline replacement operation. The phase characteristics of ethane for pipeline transport in the oilfield of China were obtained. The critical temperature is 32.79℃ and the critical pressure is 4.97 MPa.
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44

Lind, Cora. "Silver in Hybrid Membranes Facilitates Separation of Ethene and Ethane." MRS Bulletin 26, no. 5 (May 2001): 358. http://dx.doi.org/10.1557/mrs2001.83.

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45

Kim, Jihan, Li-Chiang Lin, Richard L. Martin, Joseph A. Swisher, Maciej Haranczyk, and Berend Smit. "Large-Scale Computational Screening of Zeolites for Ethane/Ethene Separation." Langmuir 28, no. 32 (August 2012): 11914–19. http://dx.doi.org/10.1021/la302230z.

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46

Koene-Cottaar, Francis H. M., and Gosse Schraa. "Anaerobic reduction of ethene to ethane in an enrichment culture." FEMS Microbiology Ecology 25, no. 3 (March 1998): 251–56. http://dx.doi.org/10.1111/j.1574-6941.1998.tb00477.x.

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47

Antoniotti, Paola, Carlo Canepa, Lorenza Operti, Roberto Rabezzana, Glauco Tonachini, and Gian Angelo Vaglio. "Gas-phase ion chemistry of silane with ethane and ethyne." Journal of Organometallic Chemistry 589, no. 2 (November 1999): 150–56. http://dx.doi.org/10.1016/s0022-328x(99)00397-6.

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48

Weidenbruch, Manfred, and Hermann Flott. "Sterisch überladene Ethane und Ethene aus Tri-tert-butylsilylmethyl-Carbenoiden." Angewandte Chemie 94, no. 5 (January 16, 2006): 384–85. http://dx.doi.org/10.1002/ange.19820940524.

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49

Atria, Ana María, Maria Teresa Garland, and Ricardo Baggio. "Three isotypic polymeric complexes with rare earth cations, but-2-enoate anions and 4,4′-(ethane-1,2-diyl)dipyridine and 4,4′-(ethene-1,2-diyl)dipyridine bridging ligands." Acta Crystallographica Section C Structural Chemistry 71, no. 4 (March 18, 2015): 301–5. http://dx.doi.org/10.1107/s2053229615004751.

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Three isotypic rare earth complexes,catena-poly[[aquabis(but-2-enoato-κ2O,O′)yttrium(III)]-bis(μ-but-2-enoato)-κ3O,O′:O;κ3O:O,O′-[aquabis(but-2-enoato-κ2O,O′)yttrium(III)]-μ-4,4′-(ethane-1,2-diyl)dipyridine-κ2N:N′], [Y2(C4H5O2)6(C12H12N2)(H2O)2], the gadolinium(III) analogue, [Gd2(C4H5O2)6(C12H12N2)(H2O)2], and the gadolinium(III) analogue with a 4,4′-(ethene-1,2-diyl)dipyridine bridging ligand, [Gd2(C4H5O2)6(C12H10N2)(H2O)2], are one-dimensional coordination polymers made up of centrosymmetric dinuclear [M(but-2-enoato)3(H2O)]2units (M= rare earth), further bridged by centrosymmetric 4,4′-(ethane-1,2-diyl)dipyridine or 4,4′-(ethene-1,2-diyl)dipyridine spacers into sets of chains parallel to the [20\overline{1}] direction. There are intra-chain and inter-chain hydrogen bonds in the structures, the former providing cohesion of the linear arrays and the latter promoting the formation of broad planes parallel to (010).
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50

Li, Y., and J. N. Armor. "Ammoxidation of ethane." Applied Catalysis A: General 188, no. 1-2 (November 1999): 211–17. http://dx.doi.org/10.1016/s0926-860x(99)00236-7.

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