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Journal articles on the topic 'Decane'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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1

Bond, Andrew D., and John E. Davies. "n-Decane." Acta Crystallographica Section E Structure Reports Online 58, no. 2 (January 31, 2002): o196—o197. http://dx.doi.org/10.1107/s1600536802001332.

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2

Baldwin, John E., Maryann E. Keene, and Rajesh Shukla. "Syntheses of dispiro[2.1.4.1]decane and dispiro[2.0.3.3]decane." Tetrahedron Letters 41, no. 49 (December 2000): 9441–43. http://dx.doi.org/10.1016/s0040-4039(00)01577-x.

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3

Baldwin, John E., Maryann E. Keene, and Rajesh Shukla. "ChemInform Abstract: Syntheses of Dispiro[2.1.4.1]decane and Dispiro[2.0.3.3]decane." ChemInform 32, no. 10 (March 6, 2001): no. http://dx.doi.org/10.1002/chin.200110083.

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4

Ghatak, Kanai L., and Camille Ganter. "The Adamantane Rearrangement of Tricyclo[4.2.2.01,5]decane to Tricyclo[5.3.0.04,8]decane." Helvetica Chimica Acta 71, no. 1 (February 3, 1988): 124–29. http://dx.doi.org/10.1002/hlca.19880710115.

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5

Wang, Yan, Xihui Ge, Minqing Zhang, Huaigong Zhu, Zijian Zhang, and Ming Wang. "Growth characteristic, guest distribution, guest ordering and the stability of urea inclusion compounds with 1-decene, n-decane and mixture of 1-decene and n-decane." Journal of Molecular Structure 1058 (January 2014): 259–64. http://dx.doi.org/10.1016/j.molstruc.2013.11.021.

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6

Awaleh, Mohamed Osman, Antonnella Badia, and François Brisse. "1,10-Bis(phenylsulfanyl)decane." Acta Crystallographica Section E Structure Reports Online 61, no. 8 (July 9, 2005): o2473—o2475. http://dx.doi.org/10.1107/s1600536805020180.

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7

Arderne, Charmaine. "Decane-1,10-diaminium dinitrate." Acta Crystallographica Section E Structure Reports Online 67, no. 11 (October 22, 2011): o3008. http://dx.doi.org/10.1107/s1600536811042929.

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8

Lee, Hyo Guk, Frank R. Groves, and Joanne M. Wolcott. "Effect of pressure on solid-liquid equilibrium for decane + octacosane, decane + p-xylene + octacosane, and decane + p-xylene + phenanthrene mixtures." Journal of Chemical & Engineering Data 38, no. 2 (April 1993): 257–59. http://dx.doi.org/10.1021/je00010a019.

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9

White, J. M., R. W. Alder, and A. G. Orpen. "1,6-Diazabicyclo[4.4.0]decane hydrate." Acta Crystallographica Section C Crystal Structure Communications 44, no. 10 (October 15, 1988): 1777–79. http://dx.doi.org/10.1107/s0108270188007048.

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10

Zhang, Qi-Long, Xin-Chen Zhu, Yun-Qian Zhang, and Bi-Xue Zhu. "1,10-Bis(2-aminophenoxy)decane." Acta Crystallographica Section E Structure Reports Online 63, no. 10 (September 15, 2007): o4039. http://dx.doi.org/10.1107/s1600536807043577.

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11

Akhter, Toheed, Humaira M. Siddiqi, Zareen Akhter, and Michael Bolte. "1,10-Bis(4-nitrophenoxy)decane." Acta Crystallographica Section E Structure Reports Online 66, no. 3 (February 6, 2010): o529. http://dx.doi.org/10.1107/s1600536810003855.

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12

Ammon, H. L., D. Zhang, C. S. Choi, O. Sandus, A. P. Marchand, and S. C. Suri. "6,6,8-Trinitropentacyclo[5.3.0.02,5.03,9.04,8]decane, C10H9N3O6." Acta Crystallographica Section C Crystal Structure Communications 41, no. 3 (March 15, 1985): 404–6. http://dx.doi.org/10.1107/s0108270185004061.

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13

Varyani, Manish, Indrajit K. Ghosh, and Suman L. Jain. "Copper ingrained poly(ethylene)glycols as cost effective and reusable media for selective 1-decene/n-decane separation." RSC Advances 5, no. 94 (2015): 77037–41. http://dx.doi.org/10.1039/c5ra11370a.

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14

Totchasov, E. D., M. Yu Nikiforov, and G. A. Al’per. "Heat capacity calculations for the decan-1-ol-n-decane system from viscosity data." Russian Journal of Physical Chemistry A 81, no. 8 (August 2007): 1346–48. http://dx.doi.org/10.1134/s0036024407080304.

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15

Stasko, Daniel, Matthew C. Davis, and Robert D. Chapman. "1,4-Diazaspiro[4.5]decane-2,3-dione." Acta Crystallographica Section E Structure Reports Online 58, no. 12 (November 22, 2002): o1384—o1386. http://dx.doi.org/10.1107/s1600536802020482.

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16

Sänger, Inge, Hans-Wolfram Lerner, and Michael Bolte. "Redetermination oftrans-2,5,7,10-tetraazabicyclo[4.4.0]decane." Acta Crystallographica Section E Structure Reports Online 60, no. 10 (September 25, 2004): o1847—o1848. http://dx.doi.org/10.1107/s1600536804022688.

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17

Jänchen, J., and H. Stach. "n-Decane adsorption on SiO2-adsorbents." Adsorption Science & Technology 3, no. 1 (March 1986): 3–10. http://dx.doi.org/10.1177/026361748600300102.

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18

Tham, W. Y., and J. M. White. "1-Azabicyclo[4.4.0]decane borine adduct." Acta Crystallographica Section C Crystal Structure Communications 50, no. 12 (December 15, 1994): 2074–76. http://dx.doi.org/10.1107/s0108270194005299.

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19

Baldwin, John E., and Rajesh Shukla. "Two Syntheses of Dispiro[2.1.3.2]decane." Organic Letters 1, no. 7 (October 1999): 1081–82. http://dx.doi.org/10.1021/ol990195j.

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20

Olchanski, Erna, and Alexander Burcat. "Decane oxidation in a shock tube." International Journal of Chemical Kinetics 38, no. 12 (2006): 703–13. http://dx.doi.org/10.1002/kin.20204.

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21

Light, Mark E., Patrick J. Murphy, Paul M. Brown, and Michael B. Hursthouse. "4,4-Dimethyl-3,5,8,10-tetraoxatricyclo[5.2.1.02,6]decane." Acta Crystallographica Section E Structure Reports Online 58, no. 5 (April 25, 2002): o560—o561. http://dx.doi.org/10.1107/s160053680200661x.

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22

Marchand, Alan P., H. K. Hariprakasha, and I. N. N. Namboothiri. "SYNTHESIS OF 2,5-DIMETHYLPENTACYCLO-[5.4.0.02,5.03,904,8]DECANE." Synthetic Communications 31, no. 12 (January 2001): 1863–69. http://dx.doi.org/10.1081/scc-100104336.

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23

Quinson, J. F., N. Tchipkam, J. Dumas, C. Bovier, J. Serughetti, C. Guizard, A. Larbot, and L. Cot. "Swelling of titania gels in decane." Journal of Non-Crystalline Solids 99, no. 1 (January 1988): 151–59. http://dx.doi.org/10.1016/0022-3093(88)90467-x.

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24

Totchasov, E. D., M. Yu Nikiforov, and G. A. Al’per. "The viscosity of the methanol-n-decane system in the region of low n-decane concentrations." Russian Journal of Physical Chemistry A 84, no. 6 (January 2010): 950–53. http://dx.doi.org/10.1134/s0036024410060117.

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25

Willman, Bert, and Amyn S. Teja. "Vapor-liquid equilibria in toluene + m-xylene, toluene + n-decane, and n-decane + m-xylene mixtures." Journal of Chemical & Engineering Data 30, no. 1 (January 1985): 116–19. http://dx.doi.org/10.1021/je00039a034.

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26

Zamora-López, Héctor S., Luis A. Galicia-Luna, Octavio Elizalde-Solis, Irma P. Hernández-Rosales, and Edgar Méndez-Lango. "Derived thermodynamic properties for the (ethanol+decane) and (carbon dioxide+ethanol+decane) systems at high pressures." Journal of Chemical Thermodynamics 55 (December 2012): 130–37. http://dx.doi.org/10.1016/j.jct.2012.06.012.

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27

Šebek, Josef, and Raivo Teeaar. "13C NMR study of the mixture MBBA/EBBA/decane: The influence of decane on the molecular ordering in the nematic phase." Collection of Czechoslovak Chemical Communications 54, no. 4 (1989): 868–77. http://dx.doi.org/10.1135/cccc19890868.

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Influence of various amounts of decane dissolved in the eutectic nematic mixture in methoxybenzylidenebutylaniline and ethoxybenzylidenebutylaniline (MBBA/EBBA) on the ordering and structure of mesomorphic molecules has been determined employing high-resolution proton enhanced 13C NMR spectroscopy. The obtained results are compared with temperature behaviour of the ordering and structure of EBBA studied by means of the same technique. Slight differences in the ordering of the phenyl parts of molecules in the dependence on temperature and on decane concentration have been observed. This contrasts with great differences observed in the behaviour of the butyl parts of mesogenic molecules. Two possible explanation of the behaviour of butyl chain atoms in the dependence on decane concentration are presented. According to one approach, conformational order parameters of the first butyl carbons increase with the increasing decane concentration. Another possibility is that decane increases the correlation between the whole molecule rotation and the internal rotation around the first butyl bond.
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28

Shamitov, A. A., I. K. Garkushin, A. V. Kolyado, and E. P. Petrov. "Phase Diagrams of the n-Decane–n-Hexadecane–Cyclododecane, n-Decane–Cyclododecane, and n-Hexadecane–Cyclododecane Systems." Russian Journal of Physical Chemistry A 92, no. 2 (February 2018): 300–303. http://dx.doi.org/10.1134/s0036024418010247.

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29

Fainerman, Valentin B., Altynay A. Sharipova, Eugene V. Aksenenko, Alexander V. Makievski, Mykola V. Nikolenko, Aliyar Javadi, Saule B. Aidarova, and Reinhard Miller. "Cooperative Effects in Surfactant Adsorption Layers at Water/Alkane Interfaces." Colloids and Interfaces 3, no. 4 (December 12, 2019): 67. http://dx.doi.org/10.3390/colloids3040067.

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In the present work, the properties of dodecyl dimethyl phosphine oxide (C12DMPO) at the water/decane interface are studied and compared with those obtained earlier at the interface to hexane. To simulate the interfacial behavior, a two-component thermodynamic model is proposed, which combines the equation of state and Frumkin isotherm for decane with the reorientation model involving the intrinsic compressibility for the surfactant. In this approach, the surface activity of decane is governed by its interaction with C12DMPO. The theory predicts the influence of decane on the decrease of the surface tension at a very low surfactant concentration for realistic values of the ratio of the adsorbed amounts of decane and surfactant. The surfactant’s distribution coefficient between the aqueous and decane phases is determined. Two types of adsorption systems were used: a decane drop immersed into the C12DMPO aqueous solution, and a water drop immersed into the C12DMPO solution in decane. To determine the distribution coefficient, a method based on the analysis of the transfer of C12DMPO between water and decane is also employed.
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30

Kaveh, Reyhaneh, Zahra Shariatinia, and Ahmad Arefazar. "Improvement of polyacrylonitrile ultrafiltration membranes' properties using decane-functionalized reduced graphene oxide nanoparticles." Water Supply 16, no. 5 (April 22, 2016): 1378–87. http://dx.doi.org/10.2166/ws.2016.059.

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The effect of decane-functionalized reduced graphene oxide (decane-rGO) was studied on the performance of polyacrylonitrile (PAN) ultrafiltration membranes. The results showed that the decane-rGO/PAN membranes had greater salt rejections relative to their corresponding GO/PAN membranes, confirming superior performance of modified decane-rGO particles. Also, the membrane with 0.2 wt% decane-rGO exhibited maximum water flux and appropriate salt rejection. The field-emission scanning electron microscopy (FE-SEM) micrographs illustrated that the sponge-like pores in the pristine PAN membrane were changed to a finger-like structure in the membrane containing up to 0.2 wt% of decane-rGO and the vertical holes were converted to horizontal holes by further increasing the decane-rGO concentration in the polymer matrix.
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31

Foley, David A., and Anita R. Maguire. "Synthetic approaches to bicyclo[5.3.0]decane sesquiterpenes." Tetrahedron 66, no. 6 (February 2010): 1131–75. http://dx.doi.org/10.1016/j.tet.2009.11.045.

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32

Bastogne, F., and C. David. "Quaternary ‘ N -alkylaldonamide–brine–decane–alcohol’ systems." Journal of Photochemistry and Photobiology A: Chemistry 136, no. 1-2 (August 2000): 93–101. http://dx.doi.org/10.1016/s1010-6030(00)00316-6.

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33

Wang, Xiao-Qiang, Jun-Feng Tong, Wen-Kui Dong, Shang-Sheng Gong, and Jian-Chao Wu. "2,2′-[1,1′-(Decane-1,10-diyldioxydinitrilo)diethylidyne]diphenol." Acta Crystallographica Section E Structure Reports Online 65, no. 8 (July 29, 2009): o2013. http://dx.doi.org/10.1107/s1600536809029341.

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34

Mehdipour, Nargess, and Saideh Bagheri. "Molecular dynamics simulation of nanoconfined n-decane." Journal of Molecular Liquids 180 (April 2013): 101–6. http://dx.doi.org/10.1016/j.molliq.2013.01.004.

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35

Blake, A. J., I. A. Fallis, R. O. Gould, S. G. Harris, S. Parsons, S. A. Ross, and M. Schröder. "1,4,7-Triazatricyclo[5.2.1.04,10]decane at 100 K." Acta Crystallographica Section C Crystal Structure Communications 51, no. 4 (April 15, 1995): 738–41. http://dx.doi.org/10.1107/s0108270194009546.

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36

Titova, N. S., S. A. Torokhov, and A. M. Starik. "On kinetic mechanisms of n-decane oxidation." Combustion, Explosion, and Shock Waves 47, no. 2 (March 2011): 129–46. http://dx.doi.org/10.1134/s0010508211020018.

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37

Czarnota, Irena. "Heat capacity of decane at high pressures." Journal of Chemical Thermodynamics 25, no. 5 (May 1993): 639–42. http://dx.doi.org/10.1006/jcht.1993.1059.

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38

Shchipunov, Yu A., and P. Schmiedel. "Electrorheological Phenomena in Lecithin–Decane–Water Mixtures." Journal of Colloid and Interface Science 179, no. 1 (April 1996): 201–6. http://dx.doi.org/10.1006/jcis.1996.0203.

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39

Watson, W. H., A. Nagl, R. P. Kashyap, A. P. Marchand, and V. Vidyasagar. "Structures of two tricyclo[5.2.1.02,6]decane derivatives." Acta Crystallographica Section C Crystal Structure Communications 46, no. 7 (July 15, 1990): 1265–68. http://dx.doi.org/10.1107/s0108270189011121.

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40

Yi, Jun-Ming, Yun-Qian Zhang, Sai-Feng Xue, and Qian-Jiang Zhu. "2,2′-(Decane-1,10-diyl)dibenzimidazolium dichloride trihydrate." Acta Crystallographica Section E Structure Reports Online 64, no. 4 (March 12, 2008): o696. http://dx.doi.org/10.1107/s160053680800617x.

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41

Troncoso, Jacobo, David Bessières, Claudio A. Cerdeiriña, E. Carballo, and Luis Romaní. "pρTxData for the Dimethyl Carbonate + Decane System." Journal of Chemical & Engineering Data 49, no. 4 (July 2004): 923–27. http://dx.doi.org/10.1021/je0342320.

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42

Kruszynski, Rafal, and Agata Trzesowska. "3,5,7-Triaza-1-azoniatricyclo[3.3.1.13,7]decane perchlorate." Acta Crystallographica Section E Structure Reports Online 60, no. 12 (November 20, 2004): o2347—o2349. http://dx.doi.org/10.1107/s1600536804029320.

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43

Hammond, Gerald B., and Raymond G. Plevey. "NEW SYNTHESIS OF 1-AZABICYCLO[5.3.0]DECANE." Organic Preparations and Procedures International 23, no. 6 (December 1991): 735–39. http://dx.doi.org/10.1080/00304949109458248.

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44

George, C., R. Gilardi, J. L. Flippen-Anderson, C. S. Choi, A. P. Marchand, and D. S. Reddy. "Structure of 6,6,10,10-tetranitropentacyclo[5.3.0.02,5.03,9.04,8]decane, C10H8N4O8." Acta Crystallographica Section C Crystal Structure Communications 41, no. 5 (May 15, 1985): 788–91. http://dx.doi.org/10.1107/s0108270185005510.

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45

Padilla, Paz, and So/ren Toxvaerd. "Fluid n‐decane undergoing planar Couette flow." Journal of Chemical Physics 97, no. 10 (November 15, 1992): 7687–94. http://dx.doi.org/10.1063/1.463488.

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46

Martens, J. A., R. Parton, L. Uytterhoeven, P. A. Jacobs, and G. F. Froment. "Selective conversion of decane into branched isomers." Applied Catalysis 76, no. 1 (September 1991): 95–116. http://dx.doi.org/10.1016/0166-9834(91)80007-j.

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47

Zhukov, Victor P., Vladislav A. Sechenov, and Andrey Yu Starikovskii. "Autoignition of n-decane at high pressure." Combustion and Flame 153, no. 1-2 (April 2008): 130–36. http://dx.doi.org/10.1016/j.combustflame.2007.09.006.

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48

Zhukov, V. P. "About kinetic modelling of n-decane autoignition." Combustion and Flame 156, no. 8 (August 2009): 1674–76. http://dx.doi.org/10.1016/j.combustflame.2009.03.015.

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49

Lim, Young Chan, and Hyun Kyu Suh. "Effect of Ambient Conditions on the Soot Generation of Decane Fuel Droplet." Journal of ILASS-Korea 19, no. 4 (December 31, 2014): 211–15. http://dx.doi.org/10.15435/jilasskr.2014.19.4.211.

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50

Adewunmi, Ahmad A., and Muhammad Shahzad Kamal. "Effect of Water/Decane Ratios and Salt on the Stability, Rheology, and Interfacial Tension of Water/Decane Emulsions." Energy & Fuels 33, no. 9 (August 30, 2019): 8456–62. http://dx.doi.org/10.1021/acs.energyfuels.9b02011.

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