Relevant bibliographies by topics / 1-methylnaphthalene

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

Academic literature on the topic '1-methylnaphthalene'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "1-methylnaphthalene"

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Sun, Hao, Kang Sun, Jianchun Jiang, and Zhenggui Gu. "Preparation of 2-Methylnaphthalene from 1-Methylnaphthalene via Catalytic Isomerization and Crystallization." Bulletin of Chemical Reaction Engineering & Catalysis 13, no. 3 (2018): 512. http://dx.doi.org/10.9767/bcrec.13.3.2650.512-519.

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Large amounts of residual 1-methylnaphthalene are generated when 2-methylnaphthalene is extracted from alkyl naphthalene. In order to transform waste into assets, this study proposes a feasible process for preparing 2-methylnaphthalene from 1-methylnaphthalene through isomerization and crystallization. The 1-methylnaphthalene isomerization was carried out in a fixed-bed reactor over mixed acids-treated HBEA zeolite. The results showed that acidic properties of catalysts and reaction temperature were associated with the 2-methylnaphthalene selectivity, yield and catalytic stability. At a high r
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Onyango, Evans O., Anne R. Kelley, David C. Qian, and Gordon W. Gribble. "Syntheses of 1-Bromo-8-methylnaphthalene and 1-Bromo-5-methylnaphthalene." Journal of Organic Chemistry 80, no. 11 (2015): 5970–72. http://dx.doi.org/10.1021/acs.joc.5b00730.

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Liang, Junjie, Qianlong Zhang, Yijun Heng, et al. "Development of a Detailed Chemical Kinetic Model for 1-Methylnaphthalene." Molecules 29, no. 23 (2024): 5660. https://doi.org/10.3390/molecules29235660.

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1-Methylnaphthalene is a critical component for constructing fuel surrogates of diesel and aviation kerosene. However, the reaction pathways of 1-methylnaphthalene included in existing detailed chemical kinetic models vary from each other, leading to discrepancies in the simulation of ignition and oxidation processes. In the present study, reaction classes and pathways involved in the combustion of 1-methylnaphthalene were analyzed, and effects of rate constants of reactions related to 1-methylnaphthalene and its significant intermediates on ignition delay times and species concentration profi
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Shaddix, C. R., K. Brezinsky, and I. Glassman. "Oxidation of 1-methylnaphthalene." Symposium (International) on Combustion 24, no. 1 (1992): 683–90. http://dx.doi.org/10.1016/s0082-0784(06)80084-6.

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Chen, Chia-Li, Mary Kacarab, Ping Tang, and David R. Cocker. "SOA formation from naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene photooxidation." Atmospheric Environment 131 (April 2016): 424–33. http://dx.doi.org/10.1016/j.atmosenv.2016.02.007.

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Rombi, E., M. G. Cutrufello, S. De Rossi, M. F. Sini, and I. Ferino. "Catalytic nitroxidation of 1-methylnaphthalene." Journal of Molecular Catalysis A: Chemical 247, no. 1-2 (2006): 171–81. http://dx.doi.org/10.1016/j.molcata.2005.11.047.

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Greenland, H., JT Pinhey, and S. Sternhell. "Synthesis and Autoxidation of 2,3,4-Trimethylnaphthalen-1-ol and Related Naphthalen-1-ols." Australian Journal of Chemistry 40, no. 2 (1987): 325. http://dx.doi.org/10.1071/ch9870325.

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The oxidation of 2-methylnaphthalene, 1,2-dimethylnaphthalene, 2,3-dimethylnaphthalene, and 1,2,3-trimethylnaphthalene by lead tetraacetate in dichloroacetic acid and chloroform gave fair to low yields of the dichloroacetyl derivatives of 2-methylnaphthalen-1-ol, 3,4-dimethylnaphthalen-1-ol, 2,3-dimethylnaphthalen-1-ol, and 2,3,4-trimethylnaphthalen-1-ol respectively. In the case of 1,3-dimethylnaphthalene, dichloroacetoxylation was not observed, and the only isolated product was the binaphthyl (10). 2,3,4-Trimethylnaphthalen-1-ol, obtained on hydrolysis of the dichloroacetyl derivative, was v
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Kukkadapu, Goutham, and Chih-Jen Sung. "Autoignition study of binary blends of n-dodecane/1-methylnaphthalene and iso-cetane/1-methylnaphthalene." Combustion and Flame 189 (March 2018): 367–77. http://dx.doi.org/10.1016/j.combustflame.2017.07.025.

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Xia, Liang Yan, Zhi Xiang Xia, Wei Tang, Hong Yan Wang, and Meng Xiang Fang. "Hydrogenation of Model Compounds Catalyzed by MCM-41-Supported Nickel Phosphide." Advanced Materials Research 864-867 (December 2013): 366–72. http://dx.doi.org/10.4028/www.scientific.net/amr.864-867.366.

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MCM-41 supported nickel phosphide (Ni2P/MCM-41) was prepared by temperature-programmed reduction of the corresponding phosphate. The catalyst activity for hydrodeoxygenation (HDO), hydrodearomatization (HDA), hydrodenitrogenation (HDN) and hydrodesulfurization (HDS) was investigated in a fixed bed reactor. O-cresol HDO, 1-methylnaphthalene HDA, quinoline HDN, dibenzothiophene HDS and simultaneous HDO, HDA, HDN, HDS were respectively tested at different temperatures with constant pressure (6.0 MPa), liquid hourly space velocity (3.0 h-1), hydrogen-to-oil volume ratio (600:1). The results indica
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Tzeng, Sheng Yuan, Vidya S. Shivatare, and Wen Bih Tzeng. "Cation Vibrations of 1-Methylnaphthalene and 2-Methylnaphthalene through Mass-Analyzed Threshold Ionization Spectroscopy." Journal of Physical Chemistry A 123, no. 28 (2019): 5969–79. http://dx.doi.org/10.1021/acs.jpca.9b03756.

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Dissertations / Theses on the topic "1-methylnaphthalene"

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Gerger, Marcus. "Centrifugal Separation of 1-Methylnaphthalene." Thesis, KTH, Skolan för kemivetenskap (CHE), 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-206732.

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In this report, modifications and experimental tests with an early stage test rig intended for producing a commercial solution to fractionating pyrolysis oil are described. The idea is to use centrifugal force to separate the formed aerosols from condensible gases with a lower volatility. A stacked disc centrifuge prototype built to work at high temperature was used. The experiment was done with a single component, 1-Methylnaphtalene (1-MN) to evaluate the functionality of the test rig. No separation was achieved, concluding that further work need to be done at different operating parameters w
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Sivena, Anastassia. "Hydrocracking reaction pathways of 1-methylnaphthalene in a continous fixed-bed reactor." Thesis, Imperial College London, 2014. http://hdl.handle.net/10044/1/29868.

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Trends in the crude oil supply have shown a decline in reserves of conventional oil, which has been offset by increasing volumes of heavy oil. Therefore, hydrocracking has become an increasingly attractive process for upgrading heavy oil fractions. This process, however, presents major challenges that have to be overcome. The present work had two principal aims. The first was to develop a new continuous fixed-bed hydrocracking reactor (CFBR) to conduct long time-on-stream experiments, ranging from 180-360 minutes. Several challenges were faced during the design and construction caused by opera
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Turner, Nicholas. "Quantifying the Toxicity of 1-Methylnaphthalene to the Shallow-Water Coral, Porites divaricata, for Use in the Target Lipid Model." NSUWorks, 2016. http://nsuworks.nova.edu/occ_stuetd/426.

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The proximity of coral reefs to coastal urban areas and shipping lanes predisposes corals to petroleum pollution from multiple sources. Previous research has evaluated petroleum toxicity to coral using a variety of methodologies, including monitoring effects of acute and chronic spills, in situ exposures, and ex situ exposures with both adult and larval stage corals. Variability in toxicant, bioassay conditions, species and other methodological disparities among studies prevents comprehensive conclusions regarding the toxicity of hydrocarbons to corals. This research evaluated the 48-hour toxi
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Wei, Chen Chih, and 陳志維. "The hydrogenation of 1-methylnaphthalene over Pt/TiO2-ZrO2 d Pd/TiO2-ZrO2." Thesis, 1994. http://ndltd.ncl.edu.tw/handle/57807637152606122928.

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Books on the topic "1-methylnaphthalene"

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United States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene. Agency for Toxic Substances Disease Registry, Division of Toxicology, Dept. of Health and Human Services, Public Health Service, 2005.

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Hisham, El-Masri, United States. Agency for Toxic Substances and Disease Registry., United States. Environmental Protection Agency., and Syracuse Research Corporation, eds. Toxicological profile for naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene. Agency for Toxic Substances and Disease Registry, 2005.

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Wilhoit, R. C. 1- and 2-methylnaphthalene and dibenzanthracenes. American Petroleum Institute, 1985.

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Methylnaphthalenes: I. 1-methylnaphthalene, 2-methylnaphthalene, II. 2,6-dimethylnaphthalene. VCH, 1992.

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Draft toxicological profile for naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene. Agency for Toxic Substances and Disease Registry, 2003.

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Toxicological profile for naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene: Draft. The Agency, 1993.

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1-And 2-Methylnaphthalene and Dibenzanthracenes (Publication, 724). Amer Petroleum Inst, 1985.

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Book chapters on the topic "1-methylnaphthalene"

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Lide, David R. "1-Methylnaphthalene." In Handbook of Organic Solvents. CRC Press, 2024. http://dx.doi.org/10.1201/9781003575191-335.

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Bährle-Rapp, Marina. "1-Acetoxy-2-Methylnaphthalene." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_65.

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Wohlfarth, Ch. "Viscosity of 1-methylnaphthalene." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_365.

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Wohlfarth, Christian. "Viscosity of 1-methylnaphthalene." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_362.

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Wohlfarth, Ch. "Refractive index of 1-methylnaphthalene." 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_318.

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Wohlfarth, Ch. "Viscosity of the mixture (1) 1-methylnaphthalene; (2) 2,2,4,4,6,8,8-heptamethylnonane." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_1861.

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Wohlfarth, Ch. "Viscosity of the mixture (1) 1H-indole; (2) 2-methylnaphthalene." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_1778.

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Stauffer, T. B., D. C. Wickman, W. G. Macintyre, and D. R. Burris. "Limitations of the Koc Concept Inferred from 1-Methylnaphthalene Sorption on Organic Coated Minerals." In Contaminated Soil ’88. Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-2807-7_21.

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Cibulka, I., L. Hnědkovský, J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Propan-2-one C3H6O + C11H10 1-Methylnaphthalene (LB2141, VMSD1111)." In Binary Liquid Systems of Nonelectrolytes. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-73584-7_1257.

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Cibulka, I., L. Hnědkovský, J. C. Fontaine, K. Sosnkowska-Kehiaian, and H. V. Kehiaian. "Volumetric Properties of the Mixture Propan-2-one C3H6O + C11H10 1-Methylnaphthalene (LB2130, VMSD1212)." In Binary Liquid Systems of Nonelectrolytes. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-73584-7_1258.

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Conference papers on the topic "1-methylnaphthalene"

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Tan, X. Q., and D. W. Pratt. "Rotationally resolved electronic spectra of 1- and 2-methylnaphthalene." In OSA Annual Meeting. Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.tuy37.

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High-resolution fluorescence-excitation spectra of the S1S0 transitions of 1- and 2-methylnaphthalene have been obtained in the collision-free environment of a molecular beam. Each spectrum is composed of two sets of spectral lines that can be fit to different rotational Hamiltonians. The two sets of lines belong to the ground torsional levels A and E, respectively. The A lines can be fit to a rigid-rotor rotational Hamiltonian; the E lines, however, are perturbed by a coupling between the torsional motion of the methyl group and the overall rotation of the molecule. The first-order and second
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Brechignac, Philippe, Zoubeida Dhaouadi, Timothy Schmidt, et al. "VISIBLE PHOTODISSOCIATION SPECTRA OF THE 1-METHYL AND 2-METHYLNAPHTHALENE CATIONS: LASER SPECTROSCOPY AND THEORETICAL SIMULATIONS." In 69th International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.wg02.

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Slavinskaya, N. A., A. Zizin, and U. Riedel. "Towards Surrogate Reaction Model Development." In ASME 2011 Turbo Expo: Turbine Technical Conference and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/gt2011-45198.

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The present paper describes the proposed strategy of fuel model design based on identification of chemical and physical criteria for the selection of initial formula of the reference fuel. The first 8 criteria established and studied in previous papers so far are combustion enthalpy, formation enthalpy, molecular weight, C/H-ratio, sooting tendency index, critical point, two-phase diagram, and distillation curve. With these criteria established, the following candidate formula of the kerosene surrogate blend is defined and optimized to adequately mimic the properties of the real fuel: 10% n-pr
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Parveg, A. S. M. Sazzad, and Albert Ratner. "Droplets Combustion Characteristics Comparison of Single Component and Multicomponent Diesel Surrogates With Petroleum-Based Commercial Diesel Fuel." In ASME 2023 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2023. http://dx.doi.org/10.1115/imece2023-113189.

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Abstract Refined, petroleum-based diesel fuel composes hundreds of hydrocarbons with distinct physio-chemical and combustion characteristics. This range of components leads to difficulties and complexities in accurate computational modeling and experimental investigations. For simplification, different surrogate fuels (single, binary or multi component) are utilized by researchers to satisfactorily mimic the target characteristics of interest (be they physio-chemical, combustion, or both). The present work is focused on combustion characteristics, and particularly those for single droplet comb
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Berry, David A., Dushyant Shekhawat, Todd H. Gardner, Maria Salazar, Daniel J. Haynes, and James J. Spivey. "Support Effects for Pt and Rh-Based Catalysts for Partial Oxidation of n-Tetradecane." In ASME 2006 4th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2006. http://dx.doi.org/10.1115/fuelcell2006-97265.

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Catalytic partial oxidation (CPOX) of liquid fuels is an attractive option for producing a hydrogen-rich gas stream for fuel cell applications. However, the high sulfur content along with aromatic compounds present in liquid fuels may deactivate reforming catalysts. Deactivation of these catalysts by carbon deposition and sulfur poisoning is a key technical challenge. The relationship between catalyst supports and deactivation have been studied here for three catalysts (Rh/Ce0.5Zr0.5O2, Pt/Ce0.5Zr0.5O2, and Pt/Al2O3) in a fixed bed catalytic reactor using a mixture of n-tetradecane, 1-methylna
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Kim, Jaeheun, Shinichi Kakami, Keiya Nishida, and Yoichi Ogata. "Effects of positive or negative dwell times of split injection on diesel spray development and mixture formation processes." In Small Engine Technology Conference & Exposition. Society of Automotive Engineers of Japan, 2020. http://dx.doi.org/10.4271/2019-32-0596.

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<div class="section abstract"><div class="htmlview paragraph">An investigation on the effect of dwell time of split injection on a diesel spray evolution and mixture formation process was carried out. A commercial 7-hole injector were used in the experiment to eliminate the possible discrepancies on the spray with single-hole research injector. Laser absorption scattering (LAS) technique was implemented for the measurement of the temporal evolution of fuel evaporation and mixture concentration. The diesel surrogate fuel consists of n-tridecane and 2.5% of 1-methylnaphthalene in vol
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Mawid, M. A., T. W. Park, B. Sekar, and C. Arana. "Detailed Chemical Kinetic Modeling of JP-8/Jet-A Ignition and Combustion." In ASME Turbo Expo 2005: Power for Land, Sea, and Air. ASMEDC, 2005. http://dx.doi.org/10.1115/gt2005-68829.

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Significant progress towards development and validation of a detailed chemical kinetic mechanism for the US Air Force JP-8 fuel is presented in this article. Three detailed chemical kinetic mechanisms for three JP-8 surrogate fuels, as given in Table I, were developed and reported in this study. The main objective is to investigate the performance of the developed three mechanisms for three different surrogate fuel blends and determine the suitability of each mechanism to chemically model the US Air Force petroleum-derived JP-fuel. The detailed JP-8 chemical kinetic reaction mechanism, we have
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Tanaka, Kotaro, Ibuki Dobashi, Satoshi Sakaida, and Mitsuru Konno. "Experimental and Modeling Study of NH <sub>3</sub> -SCR on a Hydrocarbon-Poisoned Cu-CHA Catalyst." In Energy & Propulsion Conference & Exhibition. SAE International, 2023. http://dx.doi.org/10.4271/2023-01-1659.

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&lt;div class="section abstract"&gt;&lt;div class="htmlview paragraph"&gt;A urea-selective catalytic reduction (SCR) system is used for the reduction of NOx emitted from diesel engines. Although this SCR catalyst can reduce NOx over a wide temperature range, improvements in NOx conversion at relatively low temperatures, such as under cold-start or low-load engine conditions, are necessary. A close-coupled SCR (cc-SCR), which was set just after the engine exhaust manifold, was developed to address this issue. The temperature of the SCR catalyst increases rapidly owing to the higher exhaust temp
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Yang, Shiyou, and Ruicheng Yang. "Development of a 5-Component Diesel Surrogate Chemical Kinetic Mechanism Coupled with a Semi-Detailed Soot Model with Application to Engine Combustion and Emissions Modeling." In 16th International Conference on Engines & Vehicles. SAE International, 2023. http://dx.doi.org/10.4271/2023-24-0030.

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&lt;div class="section abstract"&gt;&lt;div class="htmlview paragraph"&gt;In the present work, five surrogate components (n-Hexadecane, n-Tetradecane, Heptamethylnonane, Decalin, 1-Methylnaphthalene) are proposed to represent liquid phase of diesel fuel, and another different five surrogate components (n-Decane, n-Heptane, iso-Octane, MCH (methylcyclohexane), Toluene) are proposed to represent vapor phase of diesel fuel. For the vapor phase, a 5-component surrogate chemical kinetic mechanism has been developed and validated. In the mechanism, a recently updated H&lt;sub&gt;2&lt;/sub&gt;/O&lt;s
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Mikhailova, Anastasia N., Shadi A. Saeed, Muneer A. Suwaid, et al. "The Influence of Individual Solvents as Hydrogen Donors on the Hydrothermal Conversion of Organic Matter in Shale Rocks of Domanik Deposits." In SPE Europe Energy Conference and Exhibition. SPE, 2024. http://dx.doi.org/10.2118/220047-ms.

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Abstract The influence of individual solvents (ethyl acetate and tetralin) as hydrogen donors on the nature of the conversion of organic matter of low-permeable shale Domanik rock from the Mendym deposits of the Upper Devonian of the Tavel deposit (Tatarstan, Russia) during hydrothermal processes was studied. The experiments were carried out at a temperature of 300°C in a CO2 environment with a water content in the reaction system of a 1:1 to sample of rock and an exposure time of 24 hours. The degree of conversion of kerogen into extractable hydrocarbons was determined by Rock-Eval and therma
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