Relevant bibliographies by topics / Decane

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Decane'

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

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Journal articles on the topic "Decane"

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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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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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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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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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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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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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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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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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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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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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Dissertations / Theses on the topic "Decane"

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Sirikitputtisak, Tule. "Molecular simulation study of noble gas + n-decane binary mixtures at reservoir conditions." Thesis, University of Manchester, 2014. https://www.research.manchester.ac.uk/portal/en/theses/molecular-simulation-study-of-noble-gas--ndecane-binary-mixtures-are-reservoir-conditions(6ff06bf5-5bd4-4429-8c42-3ca96b4347c4).html.

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Carbon capture and sequestration are considered to be a temporary fix to the climate change global crisis. Following the noble gas tracers injection field experiment at Salt Creek in the state of Wyoming, USA, these tracers may be used to characterise the reservoir as a potential geological sequestration site for carbon dioxide. This study aims to investigate various thermodynamics properties of the five noble gases (Xe, Kr, Ar, Ne, and He) in n-decane at reservoir conditions (340 K – 460 K and 10 MPa – 200 MPa). The study utilises the SKS force field to describe n-decane and both Gibbs Ensemble Monte Carlo and molecular dynamics simulations were used to investigate the solubility, diffusivity, and vapour-liquid equilibrium of the five binary mixtures. The size of the noble gases was found to be important in these nonpolar mixtures where typical interactions are weak and short-ranged. The enthalpies of solvation were calculated and found to be directly correlated to the size of the solute where the energy required for the formation of a cavity to accommodate the solute is compensated by the nature of the intermolecular interaction between solvent and solute. The mixture of Ar + n-decane is of interest particularly because the sigma value for Ar is very similar to that of the CH3 group, resulting in the overall non-mononicity of several thermodynamics properties. Additionally, maxima in enthalpies of solvation were observed in Xe and Kr in n-decane solution at 200 MPa. While these maxima were observed in two different species at similar conditions, they are accommodated by unusually high uncertainties - further investigation is required before definitive conclusions can be drawn. The results from the vapour-liquid equilibrium study of the five noble gas + n-decane binary mixtures were in good agreement with the Peng-Robinson equation of state predictions. What is more, the diffusion coefficient ratios amongst the five noble gases in n-decane were investigated in light of Stoke-Einstein’s relation and Enskog’s hard-sphere relation. Three different radii of solute-solvent interaction were investigated and the best fit was observed when R =radius of solute + radius of gyration of n-decane. Additionally, the diffusion coefficients were utilised in the reservoir simulation to investigate the role of diffusion within the reservoir.
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Hodges, Stephen Lee. "The Synthesis of Hindered Aliphatic Ketones for the Future Production of Spiro [4.5] Decane Sesquiterpenes." W&M ScholarWorks, 1986. https://scholarworks.wm.edu/etd/1539625343.

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Hedin, Niklas. "NMR studies of complex fluids and solids formed by surfactants." Doctoral thesis, KTH, Chemistry, 2000. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-3033.

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NMR methods have been designed and employed in studying ofcomplex liquids and solids formed by surfactants. PGSE NMRexperiments are easily biased by convection; this artifact canbe avoided by changing the sample holder and by usingconvection-compensated pulse sequences. The temperaturedistribution within samples was controlled using thetemperature dependent order parameter for CBr2H2dissolved in a thermotropic nematic solvent.Electronic ringing that often spoils accurate NMR experimentsfor broad lines was removed by the using composite pulses andquadrupole echo sequences with appropriate phase cycles.

Field-dependent81Br and35Cl NMR relaxation studies in micellar solutions ofC16TAX surfactants showed that the structure ordynamics of the hydration shell is more influenced by thesurfactant cation for bromide than for chloride, in agreementwith their position in the Hoffmeister series. The presence ofa small but significant frequency-dependent relaxation showedthat the lateral self diffusion of the anions may be reduced ascompared to its bulk value in diluted solutions but only with afactor of 1.0 - 2.5. The ions are clearly not "bound" to thesurface. A field-dependent2H NMR relaxation study on the CTABr-α-d2and benzene-d6showed an initial one-dimensional micellargrowth followed by the appearance of microemulsion droplets onaddition of benzene. The local mobility of the benzene wasreduced when solubilized in small amounts, consistent with aninitial average location of benzene at the micellar interface.The surfactant diffusion coefficients fromconvection-compensated PGSE NMR experiments in the C12E8-D2O system showed monotonous growth of the micellesupon increasing temperature. Emulsion droplets in the C12E5-decane-D2O system where shown to coarsen according to theOstwald ripening theory after being brought out of equilibriumby a temperature drop. X-ray scattering and2H NMR line-shape and relaxation experimentssuggested that complex solids formed by a partly-sulfatedpolysaccharide and CnTAB exhibit regular ordering at both microscopicand mesoscopic length scales.

Keywords: CTAB, CTAC, C12E8, C12E5, decane, benzene, CBr2H2, polysaccharide, micelle, microemulsion, emulsion,Ostwald ripening, NMR,81Br,35Cl,2H, field- dependent spin relaxation, PGSE, selfdiffusion, convection, ringing, thermometer, generalized Blochequations, EXORCYCLE, quadrupole echo, SAXS, WAXS, cryo-TEM.

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Wu, Yue. "High-Pressure and High-Temperature Density Measurements of n-Pentane, n-Octane, 2,2,4-Trimethylpentane, Cyclooctane, n-Decane, and Toluene." VCU Scholars Compass, 2010. http://scholarscompass.vcu.edu/etd/2286.

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Information on the density of hydrocarbons at high pressures and temperatures is of great importance in many fields, such as the study of ultra-deep reservoirs up to ~240 MPa and 250°C. However, density data at such high pressures and temperatures are often not available in the literature. In this study, experimental densities are reported for n-pentane, n-octane, 2,2,4-trimethylpentane, cyclooctane, n-decane, and toluene to ~280 MPa and ~250°C. These experimental densities are in good agreement with available literature data, although the literature data for many of these fluids do not extend to the pressures and temperatures utilized in this study.
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Peres, Durand Sylvie. "Etude physico-chimique de l'élaboration de gels de titane par le procédé PEM en milieu micellaire inverse decane/TX35/H2O-H2O2." Montpellier 2, 1993. http://www.theses.fr/1993MON20207.

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Nous avons caracterise les gels de titane formes par le procede sol-gel, en milieu micellaire inverse decane/tx35/h(2)o-h(2)o(2). L'isopropoxyde de titane, solubilise dans le decane, polymerise par un mecanisme d'hydrolyse et de condensation avec une vitesse qui est controlee par la frequence des echanges inter-micellaires, et par la quantite d'eau oxygenee contenue dans les micelles inverses. L'etude physico-chimique de la solution micellaire inverse par viscosite et par diffusion de la lumiere montre qu'elle est constituee de petits agregats de forme allongee, qui ne solubilisent que 8 molecules d'eau oxygenee par molecule de tensioactif (tx35). Nous avons determine les cinetiques de gelification de l'oxyde de titane en fonction de 3 parametres experimentaux, le taux d'hydratation de la micelle, n, le taux d'hydrolyse de l'alcoxyde, h, et la molalite de l'alcoxyde, m. La formation des gels, en presence d'eau oxygenee, est plus rapide que lorsqu'on utilise l'eau, dans les memes conditions de h, n et m. L'etude physico-chimique des gels par differentes techniques comme l'analyse thermique, la diffraction des rayons x et des electrons, les isothermes d'adsorption, la microscopie electronique, la thermoporometrie et la diffusion centrale des rayons x, montrent que les gels fabriques en presence d'eau oxygenee ont une meilleure resistance mecanique que ceux formes en presence d'eau; ce sont des solides mesoporeux dont les pores, en forme de bouteille, ont un diametre de 4 nm. Les agregats primaires (dont la taille est d'environ 100 nm) sont constitues de barreaux interconnectes de 2 nm de longueur. Ils ont une structure fractale, et sont formes par un processus d'agregation amas-amas controle par la reaction chimique
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Mesquita, Francisca Maria Rodrigues. "Study of solvents alternative for aromatic extraction." Universidade Federal do CearÃ, 2015. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=14637.

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CoordenaÃÃo de AperfeÃoamento de Pessoal de NÃvel Superior
Aromatic hydrocarbons are chemical compounds of great interest in the petrochemical industry. These are commonly derived from reformed naphtha, which are in multicomponent mixtures with aliphatic hydrocarbons. The separation of these components is realized, generally, the liquid-liquid extraction process. In this process, the sulfolane is the most widely used solvent. However, this has some disadvantages such as high cost. For this reason, many studies are developed by the academic community in order to propose alternative solvents to replace the exclusive use of sulfolane by compounds that are important features like good selectivity, easy recoverability and low costs. Given the above, this study main aims to determine liquid-liquid equilibrium data (LLE) to study the ability of solvents [diethylene glycol (DEG), triethylene glycol (TEG), glycerol and 2-hydroxyethyl amine format (2-HEAF)] in extracting aromatic mixtures with aliphatic. The physical properties also of great importance in the understanding of the behavior and interactions that occur in liquid mixtures. Thus, in this study were also studied the density and viscosity of solvent extractors aromatic. The experimental methodology for the determination of LLE data was initially validated by reproducing the literature, and the results showed good agreement between these data. After the method has been validated, solubility curves and tie-lines were constructed for systems containing decane + toluene + DEG (+ TEG, + glycerol, + 2-HEAF, + sulfolane) at T = (303.15 and 333.15) K. The composition data of tie-lines, obtained experimentally, were used to calculate the selectivity parameter and the distribution coefficient. With this data, it can be concluded that all the solvents studied have a good capacity for toluene extraction from mixtures with decane. However, the glycerol has presented as the most promising solvent for aromatics extraction. Finally, the experimental data were correlated through the thermodynamic activity coefficient models, NRTL and UNIQUAC. The results were considered satisfactory, noting that the NRTL was the model that presented minor deviations in compositions. Thus, best represented the LLE data for the systems studied.
Os hidrocarbonetos aromÃticos sÃo compostos quÃmicos de grande interesse na indÃstria petroquÃmica. Estes sÃo comumente originados da nafta reformada, onde encontram-se em misturas multicomponentes com hidrocarbonetos alifÃticos. A separaÃÃo destes componentes à realizada, em sua grande maioria, pelo processo de extraÃÃo lÃquido-lÃquido. Nesse processo, o sulfolano à o solvente mais utilizado. No entanto, este apresenta algumas desvantagens, tais como alto custo. Por esse motivo, inÃmeros estudos sÃo realizados pela comunidade acadÃmica a fim de propor solventes alternativos que substituam o uso exclusivo do sulfolano por compostos que tambÃm apresentem caracterÃsticas importantes, como boa seletividade, boa recuperabilidade e baixos custos. Diante do exposto, o presente trabalho tem como principal objetivo determinar dados de equilÃbrio lÃquido-lÃquido (ELL) para estudar a capacidade dos solventes [dietilenoglicol (DEG), trietilenoglicol (TEG), glicerina e 2-hidroxietilamina formato (2-HEAF)] em extrair aromÃticos das misturas com alifÃticos. As propriedades fÃsicas tambÃm assumem extrema importÃncia no conhecimento do comportamento e das interaÃÃes que ocorrem nas misturas de lÃquidos. Deste modo, neste trabalho foram estudados a densidade e a viscosidade de solventes extratores de aromÃticos. A metodologia experimental para obtenÃÃo dos dados de ELL foi inicialmente validada reproduzindo dados da literatura, e os resultados mostraram uma boa concordÃncia entre estes dados. ApÃs a metodologia ter sido validada foram construÃdas curvas de solubilidade e tie-lines para os sistemas contendo decano + tolueno + DEG (+ TEG, + glicerina, + 2-HEAF, + sulfolano) a T = (303,15 e 333,15) K. Os dados de composiÃÃo das tie-lines, obtidos experimentalmente, foram utilizados para calcular o parÃmetro de seletividade e o coeficiente de distribuiÃÃo. De posse desses dados, pode-se concluir que todos os solventes estudados apresentam boa capacidade para extraÃÃo de tolueno a partir de misturas com decano. No entanto, a glicerina destacou-se como o solvente mais promissor para a extraÃÃo de aromÃticos apresentando os maiores valores para seletividade. Finalmente, os dados experimentais foram correlacionados atravÃs dos modelos termodinÃmicos de coeficiente de atividade, NRTL e UNIQUAC. Os resultados foram considerados satisfatÃrios, observando-se que o NRTL foi o modelo que apresentou os menores desvios na composiÃÃo. Dessa forma, representou melhor os dados de ELL para os sistemas estudados.
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Kurman, Matthew S. Cernansky N. P. Miller David L. "The preignition oxidation chemistry of n-decane and n-dodecane in a pressurized flow reactor and their use as jet fuel surrogate components /." Philadelphia, Pa. : Drexel University, 2010. http://hdl.handle.net/1860/3256.

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Gola, Annabelle. "Influence des techniques de desalumination de la zeolithe y sur ses proprietes physicochimiques et sur ses performances catalytiques en hydrocraquage du n-decane." Paris 6, 1996. http://www.theses.fr/1996PA066824.

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Des echantillons de zeolithe y desaluminee possedant une teneur constante en atomes d'aluminium de charpente et des quantites variables en especes extra-charpente ont ete prepares et caracterises. Le role des efal en hydrocraquage a ete etudie. Les methodes employees pour desaluminer la zeolithe y consistent en un steaming suivi de traitements par des solutions aqueuses d'acide nitrique, d'hexafluorosilicate d'ammonium ou d'acide ethylenediaminetetraacetique disodique. La composition chimique des echantillons obtenus montre que seules les solutions d'hexafluorosilicate d'ammonium ou d'acide ethylenediaminetetraacetique disodique permettent d'eliminer une quantite variable d'efal en conservant le rapport (si/al) de charpente constant. Differentes natures d'efal sont mises en evidence. Leur localisation, ainsi que la facilite d'extraction par les differents reactifs sont proposees. Le volume mesoporeux des echantillons traites a l'acide nitrique et l'edta disodique augmente, alors que l'hexafluorosilicate d'ammonium conduit a un depot de silice. L'acidite de la zeolithe steamee est plus faible que celle des autres, en nombre et en force. La reaction choisie pour l'etude catalytique est l'hydrocraquage du n-decane, sous haute pression d'hydrogene et a 260c. Les catalyseurs bifonctionnels sont prepares par deux methodes differentes : melange mecanique de platine sur alumine et de zeolithe, ou impregnation a sec de platine sur la zeolithe. Dans ce dernier catalyseur, la distance des sites actifs hydrogenants et acides est faible, ce qui conduit a de forts rendements en produits isomerises du n-decane. La teneur en efal, leur nature, la texture et l'acidite des zeolithes ont peu d'influence sur les performances catalytiques. Seule la zeolithe steamee conduit, dans certaines conditions, a une activite et/ou une selectivite plus faible.
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Kumar, Kamal. "Global Combustion Responses of Practical Hydrocarbon Fuels: n-Heptane, iso-Octane, n-Decane, n-Dodecane and Ethylene." online version, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=case1169746809.

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BOUASKARNE, MOHAMED. "Structure et thermodynamique des supensions colloidales : sur l'analyse de l'interaction effective dans les approches de type fluide monocomposant. exemple de la microemulsion eau/aot/decane." Paris 12, 2000. http://www.theses.fr/2000PA120023.

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L'objectif de ce travail est d'analyser le potentiel effectif intermicellaire dans les microemulsions a partir de l'exemple de la microemulsion eau/aot/decane. Dans une premiere etape, nous avons considere les approches de type de fluide effectif, dans lesquelles les parametres du potentiel effectif sont deduits de l'experience par ajustement sur les donnees de diffusion de rayonnements aux petits angles, la courbe de coexistence et les mesures de conductivite. Nous avons souligne que l'analyse structurale ne permet pas a elle seule de trancher sur la portee de l'interaction effective regnant dans ces systemes. Par ailleurs, lors de l'etude des lignes de coexistence et de percolation experimentales, il est necessaire de preserver la dependance en densite de l'intensite de cette interaction, telle qu'elle resulte de l'ajustement des facteurs de structure aux petits angles. Il apparait alors que cette interaction est d'intensite moderee, variant a la fois avec la densite et la temperature, et est de relativement longue portee. Afin de comprendre ces deux dernieres caracteristiques, nous avons suppose dans une deuxieme etape que la microemulsion est un melange binaire solute/solvant. A partir de modeles des interactions solvant-solvant et solvant-solute de type potentiel de lennard-jones ou de yukawa, nous calculons le potentiel induit par le solvant, a dilution infinie du solute, par les theories standard des melanges. A ce potentiel, nous ajoutons le potentiel direct intermicellaire (recouvrement des chaines du tensioactif, fluctuations de charge, etc) pour obtenir le potentiel total intermicellaire. Nous comparons alors les seconds coefficients du viriel de ce potentiel a celui deduit de l'analyse en terme du fluide effectif, a differentes temperatures et pour differentes combinaisons des parametres d'intensite et de portee. Nous avons souligne la necessite de traiter les differentes contributions a des echelles comparables. Il devient alors possible de comprendre au moins qualitativement l'origine de l'intensite, la portee et la variation en temperature du potentiel effectif. Cette etude souligne cependant les difficultes des approches microscopiques de ces milieux complexes.
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Books on the topic "Decane"

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. 1,3,5,7-tetoraazatorishikuro [3.3.1.13.7] dekan (betsumei hekisamechirentetoramin): 1,3,5,7-tetraazatricyclo [3.3.1.13.7] decane, hexamethylenetetramine. Tōkyō: Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2009.

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Greenberg, Arthur. Chemistry: Decade by decade. New York, NY: Facts on File, 2007.

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Eamonn, McCabe, Rader Anna, and Johnson Adrian, eds. Decade. London: Phaidon, 2010.

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Reed, Christina. Marine science: Decade by decade. New York NY: Facts On File, 2009.

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Reed, Christina. Earth science: Decade by decade. New York: Facts on File, 2008.

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Dyson, Marianne J. Space and astronomy: Decade by decade. New York: Facts on File, 2007.

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Dyson, Marianne J. Space and astronomy: Decade by decade. New York: Facts on File, 2007.

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Antonio, Ruiz José. El decano. Murcia: ERM, 1995.

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Roeseler, Karl. Last decade. Sausalito, Calif: Post-Apollo Press, 1999.

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Drucker, Johanna. Dark decade. St. Paul: Detour Press, 1995.

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Book chapters on the topic "Decane"

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Wohlfarth, Ch. "Viscosity of decane." In Supplement to IV/18, 609–12. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_357.

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Wohlfarth, Christian. "Viscosity of decane." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures, 383–84. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_355.

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Wohlfarth, Ch. "Refractive index of decane." In Refractive Indices of Pure Liquids and Binary Liquid Mixtures (Supplement to III/38), 509–12. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75291-2_314.

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Wohlfarth, Christian. "Surface tension of decane." In Surface Tension of Pure Liquids and Binary Liquid Mixtures, 179. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-48336-7_176.

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Wohlfarth, Ch. "Dielectric constant of decane." In Supplement to IV/6, 469–70. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_294.

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Wohlfarth, Ch. "Surface tension of decane." In Supplement to IV/16, 239–40. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75508-1_178.

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Wohlfarth, Christian. "Refractive index of decane." In Optical Constants, 382. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_366.

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Wohlfarth, Ch. "Viscosity of decane-1,2-diol." In Supplement to IV/18, 616. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_359.

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Wohlfarth, Ch. "Viscosity of decane-1,10-diol." In Supplement to IV/18, 617. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_360.

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Winkelmann, Jochen. "Self-diffusion coefficient of decane." In Diffusion in Gases, Liquids and Electrolytes, 373–75. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_220.

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Conference papers on the topic "Decane"

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Kumar, Kamal, Xin Hui, Apurba Das, and Chih-Jen Sung. "Autoignition, Flame Propagation, and Extinction of Binary Fuel Blends of n-Decane/Ethylene and n-Decane/Methane." In 49th AIAA Aerospace Sciences Meeting including the New Horizons Forum and Aerospace Exposition. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2011. http://dx.doi.org/10.2514/6.2011-315.

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Brocilo, D., Jen-Shih Chang, D. Ewing, H. Hirata, S. Matsumoto, and P. Fanson. "Decane reforming by a dc electrohydrodynamic atomization." In 2011 IEEE 17th International Conference on Dielectric Liquids (ICDL). IEEE, 2011. http://dx.doi.org/10.1109/icdl.2011.6015406.

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Beloni, Ervin, Vern Hoffman, and Edward Dreizin. "COMBUSTION OF DECANE-BASED SLURRIES WITH METALLIC FUEL ADDITIVES." In 45th AIAA Aerospace Sciences Meeting and Exhibit. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2007. http://dx.doi.org/10.2514/6.2007-1431.

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Zhou, Weixing, Zhenjiang Jia, Wen Bao, and Bin Yu. "Effects of Pressure on Heat Sink of n-Decane." In 10th International Energy Conversion Engineering Conference. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2012. http://dx.doi.org/10.2514/6.2012-4160.

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Hao, Min, Yongchen Song, Yuechao Zhao, Yu Liu, Bo Su, Lanlan Jiang, Xinhuan Zhou, and Lingyue Tang. "Diffusion of Carbon Dioxide in Decane by MRI Technique." In The 15th International Heat Transfer Conference. Connecticut: Begellhouse, 2014. http://dx.doi.org/10.1615/ihtc15.tpp.009220.

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Marina Weyl Costa, Dario Alviso, Nasser Darabiha, and Rogério Gonçalves. "Numerical characterization of different n-decane-ethanol blends combustion." In 23rd ABCM International Congress of Mechanical Engineering. Rio de Janeiro, Brazil: ABCM Brazilian Society of Mechanical Sciences and Engineering, 2015. http://dx.doi.org/10.20906/cps/cob-2015-2106.

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Singh, Deepti, Takayaki Nishiie, and li Qiao. "Laminar Burning Speeds and Markstein Lengths of n-Decane/Air, n-Decane/O2/He, Jet-A/Air and S-8/Air Flames." In 48th AIAA Aerospace Sciences Meeting Including the New Horizons Forum and Aerospace Exposition. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2010. http://dx.doi.org/10.2514/6.2010-951.

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Dagaut, Philippe. "Kinetics of Kerosene Combustion Over Extended Conditions: Experimental and Modeling." In ASME Turbo Expo 2006: Power for Land, Sea, and Air. ASMEDC, 2006. http://dx.doi.org/10.1115/gt2006-90015.

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The oxidation of kerosene (Jet-A1) and that of surrogate mixtures have been studied experimentally in a jet-stirred reactor at 1 to 40 atm and constant residence time, over the high temperature range 800–1300 K, and for variable equivalence ratio 0.5<φ<2). Concentration profiles of the reactants, stable intermediates, and final products have been obtained by probe sampling followed by on-line and off-line GC analyses. The oxidation of kerosene in these conditions was modeled using a detailed kinetic reaction mechanism (209 species and 1673 reactions, most of them reversible). In the modeling, kerosene was represented by four surrogate model fuels: 100% n-decane, n-decane-n-propylbenzene (74% / 26% mole), n-decane-n-propylcyclohexane (74% / 26% mole), and n-decane-n-propylbenzene-n-propylcyclohexane (74% / 15% / 11% mole). The 3-components model fuel was the most appropriate for simulating the JSR experiments. It was also successfully used to simulate the structure of a fuel-rich premixed kerosene-oxygen-nitrogen flame and ignition delays taken from the literature.
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CHOI, MUN, FREDERICK DRYER, JOHN CARD, FORMAN WILLIAMS, JOHN HAGGARD, and BRIAN BOROWSKI. "Microgravity combustion of isolated n-decane and n-heptane droplets." In 30th Aerospace Sciences Meeting and Exhibit. Reston, Virigina: American Institute of Aeronautics and Astronautics, 1992. http://dx.doi.org/10.2514/6.1992-242.

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Shakal, J., H. Ishikawa, Shinichi Goto, and D. Lee. "Flame Front Speed of a Decane Cloud under Microgravity Conditions." In International Fall Fuels and Lubricants Meeting and Exposition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1998. http://dx.doi.org/10.4271/982566.

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Reports on the topic "Decane"

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Parker, Jonathan. Spendthrift in America? On Two Decades of Decline in the U.S. Saving Rate. Cambridge, MA: National Bureau of Economic Research, July 1999. http://dx.doi.org/10.3386/w7238.

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Reinhart, Carmen, and Kenneth Rogoff. A Decade of Debt. Cambridge, MA: National Bureau of Economic Research, February 2011. http://dx.doi.org/10.3386/w16827.

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Abdo, Nabil, and Shaddin Almasri. For a Decade of Hope Not Austerity in the Middle East and North Africa: Towards a fair and inclusive recovery to fight inequality. Oxfam, August 2020. http://dx.doi.org/10.21201/2020.6355.

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Even before the coronavirus crisis struck, people in the Middle East and North Africa were protesting against the injustice and inequality wrought by a decade of austerity. The pandemic and the lockdown measures taken by governments have paralysed economies and threaten to tip millions of people into poverty, with women, refugees, migrant workers and those working in the informal economy among the worst affected. A huge increase in inequality is very likely. More austerity following this crisis will mean more uprisings, more inequality, and more conflict. This paper argues that if another decade of pain is to be averted, governments need to take immediate action to reduce inequality through providing public services to protect ordinary people by taxing the richest and guaranteeing decent work.
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Meléndez-Ortiz, Ricardo, Christophe Bellmann, and Shuaihua Cheng. A Decade in the WTO. Geneva, Switzerland: International Centre for Trade and Sustainable Development, 2011. http://dx.doi.org/10.7215/ch_ip_20111216.

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Alimi, R., A. Rahman, D. Kutscher, Y. Yang, H. Song, and K. Pentikousis. DECoupled Application Data Enroute (DECADE). RFC Editor, November 2013. http://dx.doi.org/10.17487/rfc7069.

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Wiederhold, Brenda K. Cybertherapy 2005: A Decade of VR. Fort Belvoir, VA: Defense Technical Information Center, July 2005. http://dx.doi.org/10.21236/ada436129.

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Furman, N. S. Sandia National Laboratories: The postwar decade. Office of Scientific and Technical Information (OSTI), May 1989. http://dx.doi.org/10.2172/5518557.

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Feldstein, Martin. U.S. Growth in the Decade Ahead. Cambridge, MA: National Bureau of Economic Research, January 2010. http://dx.doi.org/10.3386/w15685.

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Smith, M. A., E. E. Lewis, and E. R. Shemon. DIF3D-VARIANT 11.0: A Decade of Updates. Office of Scientific and Technical Information (OSTI), April 2014. http://dx.doi.org/10.2172/1127298.

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Song, H., N. Zong, Y. Yang, and R. Alimi. DECoupled Application Data Enroute (DECADE) Problem Statement. RFC Editor, July 2012. http://dx.doi.org/10.17487/rfc6646.

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