Academic literature on the topic 'Cyclohexane-1'

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Journal articles on the topic "Cyclohexane-1"

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Frolov, A. S., E. A. Kurganova, E. M. Yarkina, N. V. Lebedeva, G. N. Koshel, and A. S. Kalenova. "INTENSIFICATION OF THE CYCLOHEXANE LIQUID PHASE OXIDATION PROCESS." Fine Chemical Technologies 13, no. 4 (2018): 50–57. http://dx.doi.org/10.32362/2410-6593-2018-13-4-50-57.

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Liquid-phase oxidation of cyclohexane to cyclohexanol and cyclohexanone was studied in the absence of solvents under an air pressure of 0.5-5 MPa, in the temperature range 115-150 °C, catalyzed by N-hydroxyphthalimide (N-HPI). It was established for the first time that the use of N-HPI as a catalyst in place of the conventionally used metal salts of variable valence allowed a 2-3-fold increase in the conversion of the initial hydrocarbon and selectivity from 70-75 to 90%. The combined use of N-HPI with cobalt(II) acetate results in an additional increase in the conversion of cyclohexane by 30-
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Wang, Lei, Ming Qiao Zhu, Jian Gang Lu, and Hong Ding Hu. "Uncatalyzed Oxidation of Cyclohexane in the Microchannels." Key Engineering Materials 562-565 (July 2013): 1542–47. http://dx.doi.org/10.4028/www.scientific.net/kem.562-565.1542.

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The oxidation of cyclohexane in the microchannels not only improves the safety of the reaction, but also the performance of the oxidation reaction. Different gas-liquid micro mixers were used for the mixing of gas and liquid before entering into microchannels, and SIMM-V2 performed best of all. Excellent slug/plug flow can be formed in the microchannels after mixing in the gas-liquid micro mixer when the molar ratio of oxygen to cyclohexane is less than 0.5:1. The conversion of cyclohexane increased as the residence time increased, but the selectivity of cyclohexanol and cyclohexanone increase
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Lesbani, Aldes, Fatmawati Fatmawati, Risfidian Mohadi, Najma Annuria Fithri, and Dedi Rohendi. "Oxidation of Cyclohexane to Cylohexanol and Cyclohexanone Over H4[a-SiW12O40]/TiO2 Catalyst." Indonesian Journal of Chemistry 16, no. 2 (2018): 175. http://dx.doi.org/10.22146/ijc.21161.

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Oxidation of cyclohexane to cyclohexanol and cyclohexanone was carried out using H4[a-SiW12O40]/TiO2 as catalyst. In the first experiment, catalyst H4[a-SiW12O40]/TiO2 was synthesized and characterized using FTIR spectroscopy and X-Ray analysis. In the second experiment, catalyst H4[a-SiW12O40]/TiO2 was applied for conversion of cyclohexane. The conversion of cyclohexane was monitored using GC and GCMS. The results showed that H4[a-SiW12O40]/TiO2 was successfully synthesized using 1 g of H4[a-SiW12O40] and 0.5 g of TiO2. The FTIR spectrum showed vibration of H4[a-SiW12O40] appeared at 771-979
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Rekkab-Hammoumraoui, Ilhem, and Abderrahim Choukchou-Braham. "Catalytic Properties of Alumina-Supported Ruthenium, Platinum, and Cobalt Nanoparticles towards the Oxidation of Cyclohexane to Cyclohexanol and Cyclohexanone." Bulletin of Chemical Reaction Engineering & Catalysis 13, no. 1 (2018): 24. http://dx.doi.org/10.9767/bcrec.13.1.1226.24-35.

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A series of metal-loaded (Ru, Pt, Co) alumina catalysts were evaluated for the catalytic oxidation of cyclohexane using tertbutylhydroperoxide (TBHP) as oxidant and acetonitrile or acetic acid as solvent. These materials were prepared by the impregnation method and then characterized by Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP-OES), H2 chemisorption, Fourier Transformed Infrared Spectroscopy (FTIR), High-Resolution Transmission Electron Microscopy (HRTEM), and X-ray Diffraction (XRD). All the prepared materials acted as efficient catalysts. Among them, Ru/Al2O3 was found t
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Lesbani, Aldes, Menik Setyowati, Risfidian Mohadi та Dedi Rohendi. "Oxidation Of Cyclohexane To Cyclohexanol And Cyclohexanone Using H4[α-SiW12O40]/Zr As Catalyst". Molekul 11, № 1 (2016): 53. http://dx.doi.org/10.20884/1.jm.2016.11.1.194.

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Synthesis and preparation of polyoxometalate H4[α-SiW12O40].nH2O with Zr as support at various weights of Zr 0.01g; 0.05 g; 0.25 g; 0.5 g; 0.75 g; 1 g and 1.25 g to form H4[α- SiW12O40]/Zr was conducted. The compounds from preparation were characterized using FTIR spectroscopy and crystallinity analysis using X-Ray diffraction. Thus H4[α- SiW12O40]/Zr was applied as catalyst for oxidation of cyclohexane to cyclohexanol and cyclohexanone. Oxidation process was studied through reaction time, hydrogen peroxide amount, temperature, and weight of catalyst. FTIR spectrum of H4[α-SiW12O40]/Zr was app
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Hwang, Kuo Chu, and Arunachalam Sagadevan. "One-pot room-temperature conversion of cyclohexane to adipic acid by ozone and UV light." Science 346, no. 6216 (2014): 1495–98. http://dx.doi.org/10.1126/science.1259684.

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Nitric acid oxidation of cyclohexane accounts for ~95% of the worldwide adipic acid production and is also responsible for ~5 to 8% of the annual worldwide anthropogenic emission of the ozone-depleting greenhouse gas nitrous oxide (N2O). Here we report a N2O-free process for adipic acid synthesis. Treatment of neat cyclohexane, cyclohexanol, or cyclohexanone with ozone at room temperature and 1 atmosphere of pressure affords adipic acid as a solid precipitate. Addition of acidic water or exposure to ultraviolet (UV) light irradiation (or a combination of both) dramatically enhances the oxidati
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Song, Hua, Hua Lin Song, and Zai Shun Jin. "Preparation and Catalytic Performance of Co-Mo/V2O5 Composite Catalyst for Selective Oxidation of Cyclohexane." Advanced Materials Research 485 (February 2012): 76–79. http://dx.doi.org/10.4028/www.scientific.net/amr.485.76.

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A new type composite catalyst Co-Mo/V2O5 was prepared by immersion method and characterized by XRD, BET and FT-IR. The effects of Mo mass fraction, immersion time and calcination temperature on catalyst activity for oxidation of cyclohexane were investigated. Co-Mo/V2O5 subjected to immersion with 20% ammonium molybdate solution at room temperature for 1 h and calcination at 600°C exhibited the best performance. Using 0.5 ml of cyclohexane, 3 ml of hydrogen peroxide and 30 mg of catalyst at a reaction temperature of 65°C for 3 h, the cyclohexane conversion was 32.3% and the total selectivity t
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Pokutsa, Alexander, Pawel Bloniarz, Orest Fliunt, Yuliya Kubaj, Andriy Zaborovskyi, and Tomasz Paczeŝniak. "Sustainable oxidation of cyclohexane catalyzed by a VO(acac)2-oxalic acid tandem: the electrochemical motive of the process efficiency." RSC Advances 10, no. 18 (2020): 10959–71. http://dx.doi.org/10.1039/d0ra00495b.

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Cyclohexane oxidation by H<sub>2</sub>O<sub>2</sub> to cyclohexanol, cyclohexanone, and cyclohexylhydroperoxide under mild (40 °C, 1 atm) conditions is significantly enhanced in the system composed of VO(acac)<sub>2</sub> (starting catalyst) and small additives of oxalic acid (process promoter).
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Kurganova, E. A., A. S. Frolov, S. A. Kanaev, et al. "Epoxidation of cyclohexene with cyclohexyl hydroperoxide." Fine Chemical Technologies 18, no. 6 (2024): 505–16. http://dx.doi.org/10.32362/2410-6593-2023-18-6-505-516.

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Objectives. To investigate the regularities of the process of joint production of epoxycyclohexane, cyclohexanol, and cyclohexanone using the cyclohexene epoxidation reaction with cyclohexyl hydroperoxide in the presence of an ammonium paramolybdate catalyst, representing an alternative to the method of cyclohexanol and cyclohexanone synthesis by alkaline catalytic decomposition of cyclohexyl hydroperoxide.Methods. The qualitative and quantitative analysis of the obtained intermediate and target compounds was determined using modern physicochemical research methods: gas–liquid chromatography u
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Fahy, Kira, Adam Liu, Kelsie Barnard, Valerie Bright, Robert Enright, and Patrick Hoggard. "Photooxidation of Cyclohexane by Visible and Near-UV Light Catalyzed by Tetraethylammonium Tetrachloroferrate." Catalysts 8, no. 9 (2018): 403. http://dx.doi.org/10.3390/catal8090403.

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Tetraethylammonium tetrachloroferrate catalyzes the photooxidation of cyclohexane heterogeneously, exhibiting significant photocatalysis even in the visible portion of the spectrum. The photoproducts, cyclohexanol and cyclohexanone, initially develop at constant rates, implying that the ketone and the alcohol are both primary products. The yield is improved by the inclusion of 1% acetic acid in the cyclohexane. With small amounts of catalyst, the reaction rate increases with the amount of catalyst employed, but then passes through a maximum and decreases, due to increased reflection of the inc
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Dissertations / Theses on the topic "Cyclohexane-1"

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Gueudré, Laurent. "Diffusion du cyclohexane dans la Silicalite-1 : Origine et caractérisation de la résistance de surface." Lyon, Ecole normale supérieure, 2010. http://www.theses.fr/2010ENSL0580.

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L’objectif de ce travail est d’étudier plus en détail la résistance au transfert de matière à la surface des solides microporeux, en mesurant les cinétiques d’adsorption sur le système cyclohexane/Silicalite-1 par thermogravimétrie. Afin de réaliser cette thèse, un soin particulier a été accordé à la synthèse de cristaux de Silicalite-1 de différentes tailles afin de dissocier la résistance de surface de la résistance diffusionnelle intracristalline. Ces synthèses ont été réalisées de manière à obtenir des cristaux de géométrie quasi sphérique et possédant une répartition de taille homogène. L
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Rattfelt, Nyholm Jenny. "Persistency, bioaccumulation and toxicity assessment of selected brominated flame retardants." Doctoral thesis, Umeå : Department of Chemistry, Umeå University, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-22528.

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Tang, Jie. "Mesure de l'anomalie critique de l'indice de réfraction du mélange binaire nitroéthane-cyclohexane." Thèse, Université du Québec à Trois-Rivières, 1993. http://depot-e.uqtr.ca/5304/1/000601258.pdf.

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Caplinger, John N. "MematineHCI and Amino-Alkyl-Cyclohexanes (621,625) Inhibit HSV-1 in SK-N-SH Neuronal Cells." Youngstown State University / OhioLINK, 2001. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1007757941.

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Compain, Philippe. "Réarrangement thermique d'α-hydroxyimines scalémiques : approche synthétique du squelette 1-azaspiro[5,5]undécane : synthèse de γ-butyrolactones catalysée par des sels de palladium(II)". Lyon 1, 1997. http://www.theses.fr/1997LYO10120.

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L'histrionicotoxine est l'un des membres d'une famille d'alcaloides isoles a partir des secretions de grenouilles arboricoles colombiennes, les dendrobates histrionicus. Les proprietes biologiques uniques de l'histrionicotoxine, ainsi que de son analogue hydrogene la perhydrohistrionicotoxine, en font des outils de choix pour l'etude des recepteurs cholinergiques du systeme neuromusculaire. Dans le but de realiser une approche synthetique des histrionicotoxines, nous avons entame une etude sur le rearrangement thermique d'alpha-hydroxyimines scalemiques avec migration 1,2 d'un groupement allyl
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Karmal, Said. "Caractérisation des catalyseurs CoMo/Al(2)O(3) sulfurés à l'aide de réactions modèles." Poitiers, 1988. http://www.theses.fr/1988POIT2313.

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Lewis, Richard J. "The application of Cs-exchanged tungstophosphoric acid as an additive in the direct synthesis of hydrogen peroxide and the use of Au-Pd/TS-1 in a one-pot approach to cyclohexanone oxime production." Thesis, Cardiff University, 2016. http://orca.cf.ac.uk/95334/.

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The work presented within this thesis can be separated into two distinct parts. The first investigates the direct synthesis of hydrogen peroxide from molecular hydrogen and oxygen using gold-palladium supported catalysts and caesium exchanged tungstophosphoric acid as an acidic additive. The direct synthesis of H2O2 presents an environmentally friendly alternative to the current industrial, anthraquinone process. However for the direct route to be viable a variety of issues must be addressed. Primarily catalytic selectivity towards H2O2 is a major concern for the majority of catalysts active f
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Martin-Dexmier, Sophie. "Synthèse et réactivité des fluorovinylsilanes." Paris 6, 1986. http://www.theses.fr/1986PA066319.

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Synthèse des difluorovinyl silanes. Mise au point d'une des meilleures voies d'accès aux composés suivants : difluoro-1,2 alcènes, chloro-1 fluoro-2 alcènes, alcènes difluorés substitués et cétones alpha, beta -éthyléniques alpha, beta -difluorées.
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Hennequin, Laurent. "Nouvelle méthode de préparation de composés dicarbonylés-1,5 : application à la synthèse de substances naturelles." Rouen, 1986. http://www.theses.fr/1986ROUES026.

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On met au point une méthode générale de synthèse de composés delta-dicarbonylés et delta-dicarbonylés α -halogénés par action respectivement d'un éther d'énol silyle ou d'un éther d'énol silyle β-halogéné sur des carbocations fonctionnels. En milieu basique, les composés delta-dicarbonylés sont transformés en cyclohexénones, tandis que leurs anologues halogénés conduisent, selon la structure du composé de départ, à des cyclopropanes disubstitués trans ou à des spiranes hétérocycliques. Ces méthodes ont été appliquées à la synthèse d'alpha -cypérones. On a également préparé des synthons de bis-
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Chung, Hsu-Chi, and 鍾旭記. "Experimental Study on the Treatment for Waste Salt Solution of Cyclohexane Oxidation Catalyzed by Titanium Silicalite(TS-1)." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/42670857075575183421.

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Book chapters on the topic "Cyclohexane-1"

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Wohlfarth, Ch. "Viscosity of the mixture (1) cyclohexanone; (2) cyclohexane." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_1572.

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Wohlfarth, Ch. "Viscosity of the mixture (1) cyclohexane; (2) cyclohexanol." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_1581.

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Wohlfarth, Ch. "Refractive index of the mixture (1) cyclohexanone; (2) cyclohexane." In Refractive Indices of Pure Liquids and Binary Liquid Mixtures (Supplement to III/38). Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75291-2_1250.

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Wohlfarth, Ch. "Dielectric constant of the mixture (1) cyclohexanone; (2) cyclohexane." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_959.

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Winkelmann, J. "Diffusion of argon (1); cyclohexane (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1386.

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Winkelmann, J. "Diffusion of methane (1); cyclohexane (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1418.

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Winkelmann, J. "Diffusion of ethene (1); cyclohexane (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1480.

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Winkelmann, J. "Diffusion of ethane (1); cyclohexane (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1488.

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Winkelmann, J. "Diffusion of hydrogen (1); cyclohexane (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1542.

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Winkelmann, J. "Diffusion of krypton (1); cyclohexane (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1565.

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Conference papers on the topic "Cyclohexane-1"

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Gonfa, Girma, Marhaina Ismail, and Mohamad Azmi Bustam. "Benzene and cyclohexane separation using 1-butyl-3-methylimidazolium thiocyanate." In INTERNATIONAL CONFERENCE “FUNCTIONAL ANALYSIS IN INTERDISCIPLINARY APPLICATIONS” (FAIA2017). Author(s), 2017. http://dx.doi.org/10.1063/1.4999855.

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Maloney, Thad C., and Hannu Paulapuro. "Thermoporosimetry of Pulp Fibers." In The Science of Papermaking, edited by C. F. Baker. Fundamental Research Committee (FRC), Manchester, 2001. http://dx.doi.org/10.15376/frc.2001.2.897.

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This paper covers the use of thermoporosimetry to measure the pore size distribution (PSD) of pulp fibers. Thermoporosimetry is based on the melting temperature depression of an absorbate in a porous structure. A discreet or “step” melting procedure, rather than the usual continuous method, is used to melt the absorbate. This method eliminates thermal lag and gives the high temperature accuracy required for measuring large pores. Measurement of water-saturated chemical pulp fibers using this technique, combined with solute exclusion, indicates a bimodal distribution of cell wall pores. The int
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Hashim, M. A., M. Zulhaziman, M. Salleh, Emad Ali, and Mohamed K. Hadj-Kali. "Selective extraction of benzene from benzene–cyclohexane mixture using 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid." In 6TH INTERNATIONAL CONFERENCE ON ENVIRONMENT (ICENV2018): Empowering Environment and Sustainable Engineering Nexus Through Green Technology. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5117088.

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Bezborodov, Vladimir, Roman S. Dabrowski, and Jerzy Dziaduszek. "3,6-disubstituted cyclohex-2-en-1-ones as intermediates for synthesis of liquid crystals with lateral substituted cyclohexane or benzene rings." In Liquid Crystals: Materials Science and Applications, edited by Jozef Zmija. SPIE, 1995. http://dx.doi.org/10.1117/12.215547.

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Owrutsky, Jeffrey C., and Andrew P. Baronavski. "Ultrafast Infrared Study of the UV Photodissociation of Mn2(CO)10." In International Conference on Ultrafast Phenomena. Optica Publishing Group, 1996. http://dx.doi.org/10.1364/up.1996.pdp.4.

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The 310 nm photodissociation of Mn2(CO)l0 in cyclohexane has been studied using sub-picosecond IR detection near 5 μm. Photodissociation of Mn2(CO)10 results in two photoproducts, Mn(CO)5 and Mn2(CO)9 The latter undergoes an internal rearrangement to form a semi-bridged CO bond that is suspectible to solvent ligand exchange in electron donating solvents. Photodissociation dynamics have been previously studied using ultrafast UV/vis spectroscopy indicating sub-ps geminate recombination [1] and vibrational relaxation of the products. [2] This study utilizes ultrafast IR detection because it prov
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Aslanidis, Panagiotis, Dimitris Marinakis, Tina Puntervold, Vasilis Gaganis, and Nikolaos Varotsis. "Density Changes at Supercritical and Near-Critical Conditions by Increasing CO2 Content in Synthetic Hydrocarbon Mixtures – A Comparison Between Experiments and Simulation Predictions." In SPE EuropEC - Europe Energy Conference featured at the 83rd EAGE Annual Conference & Exhibition. SPE, 2022. http://dx.doi.org/10.2118/209663-ms.

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Abstract Carbon dioxide (CO2) injection is a well-known EOR-method to reduce residual oil in the pore network of oil reservoirs. It is also increasingly used as a means of mitigating the greenhouse gas emissions problem by storing it in geological formations. A key parameter to such attempts is the density of the rich CO2 mixture, which is formed downhole in the injection well, since it affects the swelling potential, oil formation volume factor, viscosity, hydrostatic gradient, fluid distribution and formation pore pressure. The density of the crude oil-CO2 mixture depends on the pressure-tem
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Kwok, Alfred S., and Richard K. Chang. "Fluorescence Seeding of Stimulated Raman Scattering in Microdroplets." In Nonlinear Optics. Optica Publishing Group, 1992. http://dx.doi.org/10.1364/nlo.1992.fb6.

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Simulated Raman scattering (SRS), in the absence of external seeding, builds up from spontaneous Raman noise. When the pump-laser pulsewidth is much longer than the dephasing time of the vibrational relaxation, the SRS spectrum is dominated by the vibrational mode with the maximum Raman gain. The depletion of the input-laser intensity by the SRS-buildup of the Raman mode with the largest gain prevents the SRS-buildup of other Raman modes with weaker gain. Selective feedback in a two-mirror resonator geometry was used to enhance the growth of SRS of the weaker 801 cm1 mode of cyclohexane in an
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Dagaut, Philippe, and Pascal Diévart. "Experimental and Modeling Study of the Combustion of Synthetic Jet Fuels: Naphtenic Cut and Blend With a GtL Jet Fuel." In ASME Turbo Expo 2016: Turbomachinery Technical Conference and Exposition. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/gt2016-56086.

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Research on the production and combustion of synthetic jet fuels has recently gained importance because of their potential for addressing security of supply and sustainable air transportation challenges. The combustion of a 100% naphtenic cut that fits with typical chemical composition of products coming from biomass or coal liquefaction (C12.64H23.64; M=175.32 g.mol−1; H/C=1.87; DCN=39; density=863.1 g.L−1) and a 50% vol. mixture with Gas to Liquid from Shell (mixture: C11.54H23.35; M=161.83 g.mol−1; H/C=2.02; DCN=46; density=800.3 g.L−1) were studied in a jetstirred reactor under the same co
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Grohmann, Jasper, Wolfgang Meier, and Manfred Aigner. "Gas Turbine Model Combustor Emissions of Liquid Single-Component Fuels." In ASME Turbo Expo 2017: Turbomachinery Technical Conference and Exposition. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/gt2017-63182.

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Alternative liquid fuels can contain hydrocarbons of different types and chain lengths and the fuel composition has an influence on combustion behavior. In this study, the influence of liquid single-component fuels on exhaust gas emissions of a gas turbine model combustor for swirl-stabilized spray flames was investigated under atmospheric pressure. The nozzle exhibited a dual-swirl geometry and a prefilming airblast atomizer. The spray was characterized by Phase Doppler Anemometry (PDA) and Mie scattering measurements and the flame CH* chemiluminescence was measured. Six single-component hydr
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Khodadadi, J. M., and Liwu Fan. "Expedited Freezing of Nanoparticle-Enhanced Phase Change Materials (NEPCM) Exhibited Through a Simple 1-D Stefan Problem Formulation." In ASME 2009 Heat Transfer Summer Conference collocated with the InterPACK09 and 3rd Energy Sustainability Conferences. ASMEDC, 2009. http://dx.doi.org/10.1115/ht2009-88409.

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An analytic/integral approach is utilized to solve a model 1-dimensional Stefan problem for a nanofluid that undergoes freezing. Initially, the isothermal nanofluid is contained in a finite slab. During the freezing process, the traveling interface separates the liquid and solid phases that possess their respective thermophysical properties. The most favorable feature of this model is that the thermal property jumps between the liquid and solid phases are accounted for. The problem is made dimensionless and is shown to depend on the thermal conductivity ratio, thermal diffusivity ratio, Stefan
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Reports on the topic "Cyclohexane-1"

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ชวนชื่น, รุ่งทิพย์, พรเพ็ญ พัฒนโสภณ та ศุภชัย เนื้อนวลสุวรรณ. การเฝ้าระวังการดื้อต่อยาฆ่าเชื้อและยาปฏิชีวนะของ Salmonella spp. และ Escherichia coli ในสายพันธุ์ที่แยกได้ในประเทศไทย : รายงานการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 2006. https://doi.org/10.58837/chula.res.2006.87.

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แยก Salmonella enterica จำนวน 257 isolates และ Escherichia coli จำนวน 60 isolates จากตัวอย่างที่ได้จาก ไก่ สุกรและสิ่งแวดล้อมในฟาร์ม ทำการหาค่า minimal inhibitory concentration (MIC) ต่อยาปฏิชีวนะและยาฆ่าเชื้อ ได้แก่ ampicillin (AMP) chloramphenicol (CHP) ciprofloxacin (CIP) erythromycin (ERY) gentamycin (GEN) tetracycline (TET) trmethoprim (TRI) benzalkonium chloride (BKC) chlorhexidine (CHX), copper sulfate (CuSO4) และ zinc chloride (ZnCl2) พบว่า salmonella 162 isolates (63.04%) และ E. coli 50 isolates (83.33%) ดื้อต่อยาปฏิชีวนะอย่างน้อยหนึ่งชนิด ค่า MIC ต่อ BKC, CHX, CUSO4 และ ZnCl2 เกาะกัน
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Pesce-Rodriguez, Rose A., and Stephanie M. Piraino. Characterization of Cyclohexanone Inclusions in Class 1 RDX. Defense Technical Information Center, 2014. http://dx.doi.org/10.21236/ada602780.

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