Academic literature on the topic 'Light alkane'
Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles
Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Light alkane.'
Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.
You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.
Journal articles on the topic "Light alkane"
Centi, G. "Selective heterogeneous oxidation of light alkanes. What differentiates alkane from alkene feedstocks?" Catalysis Letters 22, no. 1-2 (March 1993): 53–66. http://dx.doi.org/10.1007/bf00811769.
Full textBairamgulova, Rezeda I., and Elena F. Trapeznikova. "LIGHT ALKANE DEHYDROGENATION CATALYSTS." Oil and Gas Business, no. 4 (June 2019): 173. http://dx.doi.org/10.17122/ogbus-2019-4-173-196.
Full textWilcox, Esther M., George W. Roberts, and James J. Spivey. "Thermodynamics of light alkane carboxylation." Applied Catalysis A: General 226, no. 1-2 (March 2002): 317–18. http://dx.doi.org/10.1016/s0926-860x(01)00913-9.
Full textLi, Yuming, Shuting Fu, Qiyang Zhang, Hongyu Liu, and Yajun Wang. "Recent Progress of Ga-Based Catalysts for Catalytic Conversion of Light Alkanes." Catalysts 12, no. 11 (November 5, 2022): 1371. http://dx.doi.org/10.3390/catal12111371.
Full textvan den Bergh, Johan, Canan Gücüyener, Evgeny A. Pidko, Emiel J. M. Hensen, Jorge Gascon, and Freek Kapteijn. "Understanding the Anomalous Alkane Selectivity of ZIF-7 in the Separation of Light Alkane/Alkene Mixtures." Chemistry - A European Journal 17, no. 32 (July 13, 2011): 8832–40. http://dx.doi.org/10.1002/chem.201100958.
Full textLabinger, Jay A., David C. Leitch, John E. Bercaw, Mark A. Deimund, and Mark E. Davis. "Upgrading Light Hydrocarbons: A Tandem Catalytic System for Alkane/Alkene Coupling." Topics in Catalysis 58, no. 7-9 (April 2, 2015): 494–501. http://dx.doi.org/10.1007/s11244-015-0380-2.
Full textAtashi, Hossein, Mehdi Shiva, Farshad Farshchi Tabrizi, and Ali Akbar Mirzaei. "Study of Syngas Conversion to Light Olefins by Response Surface Methodology." Journal of Chemistry 2013 (2013): 1–12. http://dx.doi.org/10.1155/2013/945735.
Full textCosta, Carlos, Anais Santos, and Milena A. Vega. "Kinetics of Arab Light Crude Oil Degradation by Pseudomonas and Bacillus Strains." Water 14, no. 23 (November 22, 2022): 3802. http://dx.doi.org/10.3390/w14233802.
Full textLi, Chunyi, and Guowei Wang. "Dehydrogenation of light alkanes to mono-olefins." Chemical Society Reviews 50, no. 7 (2021): 4359–81. http://dx.doi.org/10.1039/d0cs00983k.
Full textCarotta, M. C., A. Cervi, A. Giberti, V. Guidi, C. Malagù, G. Martinelli, and D. Puzzovio. "Metal-oxide solid solutions for light alkane sensing." Sensors and Actuators B: Chemical 133, no. 2 (August 2008): 516–20. http://dx.doi.org/10.1016/j.snb.2008.03.012.
Full textDissertations / Theses on the topic "Light alkane"
Schmidt, Iver. "Design of nanoporous materials for light alkane transformation." Thesis, University of Liverpool, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.369114.
Full textWaku, Toshio. "Light alkane conversion to useful chemicals on modified ZSM5 catalysts." 京都大学 (Kyoto University), 2007. http://hdl.handle.net/2433/136343.
Full textNguyen, Luong Huu. "Development of a kinetic model for light alkane aromatisation over zeolite catalysts." Thesis, University of Bath, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419346.
Full textDerk, Alan Richard. "Understanding and Controlling Light Alkane Reactivity on Metal Oxides| Optimization Through Doping." Thesis, University of California, Santa Barbara, 2015. http://pqdtopen.proquest.com/#viewpdf?dispub=3724768.
Full textMetal oxide catalysts have numerous industrial applications and have garnered research attention. Although oxides catalyze many important reactions, their yields to products are too low to be of economic value due to low conversion and/or low selectivity. For example, some oxides can catalyze the conversion of methane to intermediates or products that are liquefiable at yields no higher than 30%. With improved yield, such a process could help reduce the trillions of cubic feet of natural gas flared every year, saving billions of dollars and millions of tonnes of greenhouse gases. To this end, one goal of this work is to understand and improve the catalytic activity of oxides by substituting a small fraction of the cations of a "host oxide" with a different cation, a "dopant." This substitution disrupts chemical bonding at the surface of the host oxide, which can improve reactant and lattice oxygen activation where the reaction takes place. Another goal of this work is to combine catalysts with metal oxides reactants to improve thermodynamic limitations. Outstanding challenges for the study of doped metal oxide catalysts include (1) selection of dopants to ix synthesize within a host oxide and (2) understanding the nature of the surface of the doped oxide during reaction.
Herein, strongly coupled theoretical calculations and experimental techniques are employed to design, synthesize, characterize, and catalytically analyze doped oxide catalysts for the optimization of light alkane conversion processes. Density Functional Theory calculations are used to predict different energies believed to be involved in the reaction mechanism. These parameters offer valuable suggestions on which dopants may perform with highest yield and activity and why. Synthesis is accomplished using a combination of wet chemical techniques, suited specifically for the preparation of doped (rather than supported or mixed) metal oxide catalysts of high surface area and high reactivity. Characterization is paramount in any doped-oxide investigation to determine if the catalyst under reaction conditions is truly doped or merely small clusters of supported catalyst. With that goal, diffraction, X-ray, electron microscopies, infrared spectroscopy, and chemical probes are used to determine the nanoscopic nature of the catalysts. Additional novel measurement techniques, such as transient oxidation reaction spectroscopy, determined the nature of the active site's oxidation state.
Al-Sayari, Saleh Abdullah. "Synthesis of active supported gold catalysts for CO oxidation and light alkane activation." Thesis, Cardiff University, 2006. http://orca.cf.ac.uk/56051/.
Full textLøften, Thomas. "Catalytic isomerization of light alkanes." Doctoral thesis, Norwegian University of Science and Technology, Department of Chemical Engineering, 2004. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-1909.
Full textIn recent years the levels of sulfur and benzene in the gasoline pool have been reduced, and in the future there may also be new regulations on vapor pressure and the level of aromatics and olefins as well. The limitations on vapor pressure and aromatics will lead to reduced use of C4 and reformate respectively. The branched isomers of C5 and C6 alkanes have high octane numbers compared to the straight chain isomers, and are consequently valuable additives to the gasoline pool. To maintain the octane rating, it is predicted that an increased share of isomerate will be added to the gasoline pool.
Today there is a well established isomerization technology with platinum on chlorided alumina as the commercial catalyst for both isomerization of n-butane and of the C5/C6 fraction. This catalyst is very sensitive to catalyst poisons like water and sulfur, and strict feed pretreatment is required. Zeolites promoted by platinum are alternatives as isomerization catalysts, and has replaced Pt/alumina catalysts to some extent. The Pt/zeolite catalyst is more resistant to water and sulfur compounds in the feed, but it is less active than platinum on chlorided alumina. It does therefore require a higher reaction temperature, which is unfortunate since the formation of the branched isomers of the alkanes is thermodynamically favored by a low temperature.
Because of the limitations of the two types of isomerization catalysts, there is a search for a new catalyst that is resistant to sulfur and water in the feed and is highly active so it can be operated at low temperature. A new type of catalyst that seems to be promising in that respect is sulfated zirconia.
The first part of this study focuses on a series of iron and manganese promoted SZ catalysts. The catalysts were characterized by various techniques such as XRD, TGA, N2 adsorption and IR spectroscopy of adsorbed pyridine. The catalytic activity in n-butane isomerization at 250°C and atmospheric pressure was compared to the physical and chemical properties of the samples. No promoting effect of iron and manganese was found when n-butane was diluted in nitrogen. When nitrogen was replaced by hydrogen as the diluting gas the activity of the unpromoted SZ sample was dramatically lowered, while the activity of the promoted catalyst was not significantly changed.
If we only consider the promoted samples, the catalytic activity increases with increasing iron/manganese ratio. We also observe that the activity of the samples is clearly correlated with the number of strong Brønsted acid sites. The total number of strong acid sites (i.e. the sum of Brønsted and Lewis sites) does not change significantly when the promoter content is changing, hence no correlation between catalytic activity and the total number of acid sites is found. This underlines the importance of discrimination between Lewis and Brønsted acidity when characterizing the acidity of the samples.
The second part of this study is focused on a series of noble metal promoted sulfated zirconia. Their catalytic activity in n-hexane isomerization at high pressures was compared to a commercial Pt/zeolite catalyst. Among the noble metal promoted samples the catalyst promoted with platinum was the most active. The samples promoted with rhodium, ruthenium and iridium showed equal activity.
Common for all the noble metal promoted catalysts is the large increase in activity when catalysts are reduced with hydrogen compared to when they are pretreated in helium. The increase in activity is most likely connected to the reduction of the metal oxides of the promoters to ensure that the promoters are in the metallic state. Reduction at too high temperatures does however give lower activity. This is probably due to the reduction of surface sulfate groups leading to a loss in acid sites.
The commercial sample was considerably less active than the sample of platinum promoted sulfated zirconia. The commercial catalyst was however more stable than the PtSZ catalyst. All the sulfated zirconia catalysts deactivated, but the initial activity could be regenerated by reoxidation at 450°C followed by reduction at 300°C. The promotion with noble metals appears to inhibit coke formation on the catalyst. But, the main cause of deactivation of the platinum promoted sample is most likely the reduction of sulfate species leading to a loss of acid sites.
The kinetic study of the catalysts indicates that the n-hexane isomerization proceeds via a classical bifunctional mechanism where the role of the promoting metal is to produce alkenes, which are subsequently protonated on the acid sites. The reaction orders of hydrogen, n-hexane and total pressure are all in accordance with this mechanism. The activation energies of the catalysts are within the typical range of bifunctional catalysts.
All catalysts, except the unpromoted SZ sample, showed close to 100% selectivity to branched hexane isomers and a similar distribution of these isomers. The isomer distribution being the same for both the noble metal promoted catalyst and the Pt/zeolite is another indication that the isomerization proceeds via the bifunctional mechanism over the promoted samples. The different selectivity of the unpromoted SZ catalyst indicates that the isomerization proceeds via a different pathway over this catalyst; this is probably a pure acidic mechanism
The acidity characterization can not explain the differences in isomerization activity. It is however likely that the activity of the promoting metals in the dehydrogenation of alkanes is important since the classical bifunctional mechanism is prevailing.
Pithan, Linus. "On the role of external stimuli to tailor growth of organic thin films." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät, 2017. http://dx.doi.org/10.18452/17749.
Full textThe research performed in the framework of this thesis focuses on new strategies to effectively control the growth of crystalline thin films of functional organic molecules and attributes the quest for additional growth control parameters in organic molecular beam deposition (OMBD). First the influence of light on the growth process of the sexithiophene (6T) is studied. We find that 6T thin films deposited as conventional in dark environments on KCl exhibit a bimodal growth with phase coexistence of two crystal polymorphs. In contrast, films grown under illumination with 532 nm light show increased phase purity. Further, we establish light-directed molecular self-assembly (LDSA) to generate permanently aligned thin films of tetracene (C18H12) and demonstrate direct patterning with light. Polarized light illumination leads to azimuthally photoaligned films on isotropic, amorphous substrates. Thus, LDSA can be regarded as a new degree of freedom in the quest for control-parameters in organic thin film growth. Next the impact of dynamic temperature oscillations on the time scales of molecular monolayer growth during organic molecular beam deposition is discussed. We strongly increase the island density during nucleation and selectively increase interlayer diffusion at later stages of monolayer growth. We analyse the interplay between molecular interlayer transport and island sizes to understand kinetic processes during growth. In a fourth experiment we show how thermal annealing can be used to improve smoothness and to increase the lateral size of crystalline islands of n-alkane (TTC, C44H90) films. We employ real-time optical phase contrast microscopy to track the diffusion across monomolecular step edges which causes the unusual smoothing during annealing. We rationalise the smoothing behaviour with the highly anisotropic attachment energies and low surface energies of TTC.
Ramakrishnan, Ayyappan. "Visible light induced catalytic sulfoxidation of alkanes." [S.l.] : [s.n.], 2006. http://deposit.ddb.de/cgi-bin/dokserv?idn=981136915.
Full textSu, Yee San 1977. "The heterogeneous partial oxidation of light alkanes." Thesis, Massachusetts Institute of Technology, 2004. http://hdl.handle.net/1721.1/28306.
Full textIncludes bibliographical references.
(cont.) With this approach, an upper bound on the yield for OCM was computed. Results showed that even with optimal surface chemistry, strict limits existed on the attainable yield. Surface energetics necessary for superior OCM performance were identified and the origins of these requirements elucidated. The resulting upper bound on OCM yield under conventional, packed-bed, continuous-feed operation was found to be 28%. The catalytic properties of LiCl/sulfated ZrO₂-based catalysts were explored for ODHE. LiCl was shown to strongly interact with the acid sites on sulfated ZrO₂ (SZ), influencing its catalytic behavior. Two approaches were taken to modify the nature/strength of the LiCl-support interaction. Firstly, LiCl/Nd₂O₃-impregnated MoO/ZrO₂ and WOx/ZrO₂ were examined. Unlike SZ, these supports allowed for the tailoring of MoO[sub]x and WO[sub]x surface densities, which in turn drastically altered their ODHE performance. The poor stability of these supports, however, rendered them inferior to SZ. Secondly, the effects of dopant incorporation on the catalytic behavior of LiCI/MO,/SZ were studied. Si-doped ZrO₂-based catalysts synthesized via the sol-gel method were found to exhibit superior activity, selectivity and stability for ODHE. Sulfate decomposition experiments related the ODHE activity of these materials to the influence of the Si dopant on the sulfate binding strength. The sol-gel synthesis conditions were optimized with respect to sol pH, water:alkoxide ratio and silicon precursor, achieving improved catalyst homogeneity and enhanced ODHE performance ...
Within the petrochemical industry, a sizeable economic incentive exists for the upgrading of low-value, light alkanes. For instance, the dehydrogenation of ethane to ethene is of considerable interest due to ethene's use as a polymeric and chemical precursor. Partial oxidation provides an attractive alternative to standard pyrolysis methods for alkane-to-alkene conversion. Unlike pyrolysis, partial oxidative routes are largely unaffected by coke formation and have the added benefit of exothermicity. With the inclusion of oxygen as a reactant, however, numerous additional reaction pathways result. Among these, the presence of parallel and consecutive reaction channels to CO[sub]x products is of major concern. For this reason, previous efforts to create selective partial oxidation catalysts with high activity have typically fallen below economic feasibility requirements. This thesis focuses on the following alkane-to-alkene transformation reactions: Oxidative Coupling of Methane (OCM): 2CH₄ + O₂ <--> C₂H₄ + 2 H₂O Oxidative Dehydrogenation of Ethane (ODHE): C₂H₆ + 1/2 O₂ <--> C₂H₄ + H₂O Oxidative Dehydrogenation of Propane (ODHP): C₃H₈ + 1/2 O₂ <--> C₃H₆ + H₂O. Regarding OCM, an approach was presented for determining an upper bound on the yield of a catalytic process, which allowed for variations in the catalytic chemistry. Scaling and thermodynamic arguments were used to set parameters of an elementary step surface mechanism at values resulting in optimal yields, subjected only to physical constraints. Remaining unknowns were treated as independent variables and varied over a broad range. The result was a set of thermodynamically consistent mechanisms with optimal kinetics that could be incorporated into reactor-transport models.
by Yee San Su.
Ph.D.
Du, Xian. "Catalysis for CO2 activation reactions with light alkanes." Thesis, University of Oxford, 2016. https://ora.ox.ac.uk/objects/uuid:924c17f7-5b71-4e70-b304-e0686d0413ea.
Full textBooks on the topic "Light alkane"
Derouane, Eric G., Jerzy Haber, Francisco Lemos, Fernando Ramôa Ribeiro, and Michel Guisnet, eds. Catalytic Activation and Functionalisation of Light Alkanes. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-017-0982-8.
Full textG, Derouane E., and North Atlantic Treaty Organization. Scientific Affairs Division., eds. Advances and challenges: Catalytic activation and functionalisation of light alkanes. Dordrecht: Boston, Mass., 1998.
Find full textOrganization, World Health, ed. Calcium and magnesium in drinking-water: Public health significance. Geneva, Switzerland: World Health Organization, 2009.
Find full textDerouane, Eric G. Catalytic Activation and Functionalisation of Light Alkanes: Advances and Challenges. Springer, 2010.
Find full text(Editor), E. G. Derouane, Jerzy Haber (Editor), Francisco Lemos (Editor), Fernando Ramôa Ribeiro (Editor), and Michel Guisnet (Editor), eds. Catalytic Activation and Functionalisation of Light Alkanes - Advances and Challenges. Springer, 1998.
Find full textGuisnet, Michel, Fernando Ramôa Ribeiro, E. G. Derouane, Jerzy Haber, and Francisco Lemos. Catalytic Activation and Functionalisation of Light Alkanes: Advances and Challenges. Springer, 2013.
Find full textDerouane, E. G., Jerzy Haber, and Francisco Lemos. Catalytic Activation and Functionalisation of Light Alkanes: Advances and Challenges. Springer, 2014.
Find full textBannatyne-Cugnet, Jo. Grampa's Alkali (Northern Lights Young Novels). Red Deer Press, 2002.
Find full textBannatyne-Cugnet, Jo. Grampa's Alkali (Northern Lights Books for Children). Tandem Library, 1993.
Find full textBook chapters on the topic "Light alkane"
Sorokin, Alexander B. "Recent Developments of Bioinspired Approaches to Functionalization of Light Alkanes." In Alkane Functionalization, 189–210. Chichester, UK: John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781119379256.ch10.
Full textDjéga-Mariadassou, G. "Alkane Activation by Pseudo-Metals." In Catalytic Activation and Functionalisation of Light Alkanes, 333–67. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-017-0982-8_13.
Full textSolymosi, F. "Molecular Chemistry of Alkane Activation." In Catalytic Activation and Functionalisation of Light Alkanes, 369–88. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-017-0982-8_14.
Full textGuerrero-Pérez, M. Olga. "Mixed-Oxide Nanocatalysts for Light Alkane Activation." In Nanocatalysis, 115–34. Boca Raton, FL : CRC Press, Taylor & Francis Group, 2019. | “A science publishers book.”: CRC Press, 2019. http://dx.doi.org/10.1201/9781315202990-5.
Full textZhou, X. P., S. Q. Zhou, W. D. Zhang, Z. S. Chao, W. Z. Weng, R. Q. Long, D. L. Tang, et al. "Methane and Light Alkane (C2-C4) Conversion Over Metal Fluoride-Metal Oxide Catalyst System in Presence of Oxygen." In Methane and Alkane Conversion Chemistry, 19–30. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4615-1807-5_2.
Full textLabinger, Jay A., and Graham J. Hutchings. "Report of the Workshop on Challenges and Opportunities in Light Alkane Activation." In Catalytic Activation and Functionalisation of Light Alkanes, 455–65. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-017-0982-8_25.
Full textKnops-Gerrits, P. P., A. M. Bavel, G. Langouche, and P. A. Jacobs. "Mono- and Binuclear Iron Complexes in Zeolites and Mesoporous Oxides as Biomimetic Alkane Oxidation Catalysts." In Catalytic Activation and Functionalisation of Light Alkanes, 215–57. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-017-0982-8_9.
Full textHutchings, G. J. "Selective Oxidation of Light Alkanes." In Catalytic Activation and Functionalisation of Light Alkanes, 125–56. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-017-0982-8_6.
Full textPanov, Andrey, Sergey Vinogradov, and Svyatoslav Engalychev. "Evolutional Development of Alkaline Aluminosilicates Processing Technology." In Light Metals 2017, 9–16. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-51541-0_2.
Full textKozhevnikov, Ivan V. "Activation of Light Alkanes: Past and Present." In Catalytic Activation and Functionalisation of Light Alkanes, 75–87. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-017-0982-8_3.
Full textConference papers on the topic "Light alkane"
Yin, Sudong, Yanglin Pan, and Zhongchao Tan. "Catalytic Hydrothermal Conversion of Glucose to Light Petroleum Alkanes." In ASME 2010 4th International Conference on Energy Sustainability. ASMEDC, 2010. http://dx.doi.org/10.1115/es2010-90433.
Full textSnytnikov, V. N. "LIGHT ALKANE CONVERSION IN A LASER REACTOR." In INTERNATIONAL CONFERENCE ON THE METHODS OF AEROPHYSICAL RESEARCH. Novosibirsk: Издательство Сибирского отделения РАН, 2022. http://dx.doi.org/10.53954/9785604788974_157.
Full textIngebrigtsen, S., N. Bonifaci, A. Denat, and O. Lesaint. "Spectral analysis of light emitted from streamers in chlorinated alkane & alkene liquids." In 2008 IEEE International Conference on Dielectric Liquids (ICDL 2008). IEEE, 2008. http://dx.doi.org/10.1109/icdl.2008.4622485.
Full textCERVI, A., M. C. CAROTTA, A. GIBERTI, V. GUIDI, C. MALAGÙ, G. MARTINELLI, and D. PUZZOVIO. "METAL-OXIDE SOLID SOLUTIONS FOR LIGHT ALKANE SENSING." In Proceedings of the 13th Italian Conference. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812835987_0025.
Full textZhou, Daiyu, Liming Lian, Zangyuan Wu, Gengping Yan, Wei Zhou, Guangqiang Shao, Haihang Sun, et al. "Optimization Design and Evaluation of Improved Miscible Assistants for CO2 Flooding and the Application in Pilot in L Reservoir." In International Petroleum Technology Conference. IPTC, 2022. http://dx.doi.org/10.2523/iptc-22244-ms.
Full textVan Reempts, J., B. Van Deuren, M. Borqers, and F. De Clerck. "R 68 070, A COMBINED TXA2-SYNTHETASE/TXA2-PROSTAGLANDIN ENDOPEROXIDE RECEPTOR INHIBITOR. REDUCES CEREBRAL INFARCT SIZE AFTER PHOTOCHEMICALLY INITIATED THROMBOSIS IN SPONTANEOUSLY HYPERTENSIVE RATS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643470.
Full textWitkowski, M., M. Zawada, M. Bober, S. Bilicki, R. Munoz-Rodriguez, V. Singh, M. A. Butt, A. Tonoyan, D. Dziczek, and R. Ciuryo. "Interactions of Ultra-cold Alkaline-earth-like and Alkali Atoms with Light." In 2019 Joint Conference of the IEEE International Frequency Control Symposium anEuropean Frequency and Time Forum (EFTF/IFC). IEEE, 2019. http://dx.doi.org/10.1109/fcs.2019.8856001.
Full textGan, Yunyan, Li Chen, Jinqing Zhang, Oliver C. Mullins, Zhenghe Yan, Ji Tian, Xiaofei Gao, Weihua Chen, Haizhang Yang, and Jianrong Hao. "A Novel Reservoir Forming Mechanism with Wax-Out Cryo Trapping." In International Petroleum Technology Conference. IPTC, 2022. http://dx.doi.org/10.2523/iptc-21918-ms.
Full textKoroliov, Anton, Karolina Varsockaja, Jonas Reklaitis, Artūras Plukis, and Vidmantas Remeikis. "X-ray Pulse Emission of Alkali Metal Halide Salts Irradiated by Femtosecond Laser Pulses." In Compact EUV & X-ray Light Sources. Washington, D.C.: OSA, 2020. http://dx.doi.org/10.1364/euvxray.2020.jw4a.5.
Full textPadmaja, G., T. Goverdhan Reddy, P. Kistaiah, P. Predeep, Mrinal Thakur, and M. K. Ravi Varma. "On the Electron Paramagnetic Resonance Studies in Mixed Alkali Borate Glasses." In OPTICS: PHENOMENA, MATERIALS, DEVICES, AND CHARACTERIZATION: OPTICS 2011: International Conference on Light. AIP, 2011. http://dx.doi.org/10.1063/1.3643605.
Full textReports on the topic "Light alkane"
Lyons, J. E. Catalytic conversion of light alkanes. Office of Scientific and Technical Information (OSTI), June 1992. http://dx.doi.org/10.2172/7090637.
Full textLyons, J. E. Catalytic conversion of light alkanes: Proof of concept stage. Office of Scientific and Technical Information (OSTI), June 1995. http://dx.doi.org/10.2172/67783.
Full textLyons, J. E. Catalytic conversion of light alkanes. [Methane, ethane, propane and butanes]. Office of Scientific and Technical Information (OSTI), September 1992. http://dx.doi.org/10.2172/7090643.
Full textBiscardi, J., P. T. Bowden, V. A. Durante, P. E. Jr Ellis, H. B. Gray, R. G. Gorbey, R. C. Hayes, et al. Catalytic conversion of light alkanes: Quarterly report, January 1-March 31, 1992. Office of Scientific and Technical Information (OSTI), May 1997. http://dx.doi.org/10.2172/467133.
Full textLyons, J. E. Catalytic conversion of light alkanes. Quarterly progress report, April 1--June 30, 1992. Office of Scientific and Technical Information (OSTI), June 1992. http://dx.doi.org/10.2172/10133009.
Full textWasan, D. T. Surfactant-enhanced alkaline flooding for light oil recovery. Final report. Office of Scientific and Technical Information (OSTI), May 1996. http://dx.doi.org/10.2172/240455.
Full textLyons, J. E. Catalytic conversion of light alkanes. Quarterly progress report, July 1, 1992--September 30, 1992. Office of Scientific and Technical Information (OSTI), September 1992. http://dx.doi.org/10.2172/10131893.
Full textWasan, D. T. Surfactant-enhanced alkaline flooding for light oil recovery. [Annual report], 1993--1994. Office of Scientific and Technical Information (OSTI), March 1995. http://dx.doi.org/10.2172/32596.
Full textWasan, D. T. Surfactant-enhanced alkaline flooding for light oil recovery. Final report 1994--1995. Office of Scientific and Technical Information (OSTI), December 1995. http://dx.doi.org/10.2172/541805.
Full textWasan, D. T. Surfactant-enhanced alkaline flooding for light oil recovery. Annual report, 1992--1993. Office of Scientific and Technical Information (OSTI), August 1994. http://dx.doi.org/10.2172/10176348.
Full text