Log in

Relevant bibliographies by topics / 1-methylnaphthalene / Journal articles

To see the other types of publications on this topic, follow the link: 1-methylnaphthalene.

Journal articles on the topic '1-methylnaphthalene'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic '1-methylnaphthalene.'

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.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

2

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

4

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

8

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

10

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

Calvert, JL, L. Eberson, MP Hartshorn, n. Maclaga, and WT Robinson. "Photochemical Nitration by Tetranitromethane. XVII. The Regiochemistry of Adduct Formation in the Photochemical Reaction of 1-Methylnaphthalene and Tetranitromethane." Australian Journal of Chemistry 47, no. 8 (1994): 1591. http://dx.doi.org/10.1071/ch9941591.

Full text

Abstract:

Photolysis of the 1-methylnaphthalene/tetranitromethane charge-transfer complex yields the triad of 1-methylnaphthalene radical cation, nitrogen dioxide and trinitromethanide ion. Recombination of this triad gives predominantly 4-methyl-t-2-nitro-r-1-trinitromethyl-1,2- dihydronaphthalene (1), the epimeric 1-methyl-1-nitro-4-trinitromethyl-1,4-dihydronaphtha-lenes (2) and (3), 8-methyl-c-4-trinitromethyl-1,4-dihydronaphthalen-r-l-ol (4), nitro cyclo -adduct (5), 8-methyl-c-4-trinitromethyl-1,4-dihydronaphthalen-r-l-ol (6), hydroxy cyclo-adduct (7) and 4-methyl-t-1-trinitromethyl-1,2-dihydronap

APA, Harvard, Vancouver, ISO, and other styles

12

Nobusawa, Tatsuya, Yoshinori Takagi, and Toshihide Suzuki. "Isomerization of 1-Methylnaphthalene over HY Zeolite." KAGAKU KOGAKU RONBUNSHU 21, no. 6 (1995): 1090–95. http://dx.doi.org/10.1252/kakoronbunshu.21.1090.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Abida, Indah Wahyuni, Sri Andayani, Uun Yanuhar, and Hardoko. "Bioaccumulation of Polycyclic Aromatic Hydrocarbons (PAHs) in simping scallops (Placuna placenta) from the Waters of Socah and Ujungpangkah, East Java." E3S Web of Conferences 442 (2023): 01012. http://dx.doi.org/10.1051/e3sconf/202344201012.

Full text

Abstract:

The study aimed to investigate the bioaccumulation of Polycyclic Aromatic Hydrocarbons (PAHs) in Placuna placenta scallops from Socah and Ujungpangkah waters in East Java, Indonesia. The research involved sampling from Station 1 at Ujungpangkah and Station 2 at Socah waters. Water, sediment, and Simping scallops were sampled twice, in December 2018 and January 2019. The analysis method used Gas Chromatography-Mass Spectrometry (GC-MS). The analysis results indicated that the total PAHs concentration was higher in Ujungpangkah waters compared to Socah waters. In line with the result of sediment

APA, Harvard, Vancouver, ISO, and other styles

14

Annweiler, Eva, Arne Materna, Michael Safinowski, et al. "Anaerobic Degradation of 2-Methylnaphthalene by a Sulfate-Reducing Enrichment Culture." Applied and Environmental Microbiology 66, no. 12 (2000): 5329–33. http://dx.doi.org/10.1128/aem.66.12.5329-5333.2000.

Full text

Abstract:

ABSTRACT Anaerobic degradation of 2-methylnaphthalene was investigated with a sulfate-reducing enrichment culture. Metabolite analyses revealed two groups of degradation products. The first group comprised two succinic acid adducts which were identified as naphthyl-2-methyl-succinic acid and naphthyl-2-methylene-succinic acid by comparison with chemically synthesized reference compounds. Naphthyl-2-methyl-succinic acid accumulated to 0.5 μM in culture supernatants. Production of naphthyl-2-methyl-succinic acid was analyzed in enzyme assays with dense cell suspensions. The conversion of 2-methy

APA, Harvard, Vancouver, ISO, and other styles

15

Fu, J., I. Ferino, R. Monaci, E. Rombi, V. Solinas, and L. Fornib. "Ammoxidation of 1-methylnaphthalene over CuNa-Mordenite zeolites." Applied Catalysis A: General 154, no. 1-2 (1997): 241–55. http://dx.doi.org/10.1016/s0926-860x(96)00357-2.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Popova, Z., M. Yankov, L. Dimitrov, and I. Chervenkov. "Isomerization and disproportionation of 1-methylnaphthalene on zeolites." Reaction Kinetics & Catalysis Letters 52, no. 1 (1994): 51–58. http://dx.doi.org/10.1007/bf02129849.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Chan, A. W. H., K. E. Kautzman, P. S. Chhabra, et al. "Secondary organic aerosol formation from photooxidation of naphthalene and alkylnaphthalenes: implications for oxidation of intermediate volatility organic compounds (IVOCs)." Atmospheric Chemistry and Physics Discussions 9, no. 1 (2009): 1873–905. http://dx.doi.org/10.5194/acpd-9-1873-2009.

Full text

Abstract:

Abstract. Current atmospheric models do not include secondary organic aerosol (SOA) production from gas-phase reactions of polycyclic aromatic hydrocarbons (PAHs). Recent studies have shown that primary semivolatile emissions, previously assumed to be inert, undergo oxidation in the gas phase, leading to SOA formation. This opens the possibility that low-volatility gas-phase precursors are a potentially large source of SOA. In this work, SOA formation from gas-phase photooxidation of naphthalene, 1-methylnaphthalene (1-MN), 2-methylnaphthalene (2-MN), and 1,2-dimethylnaphthalene (1,2-DMN) is s

APA, Harvard, Vancouver, ISO, and other styles

18

Camargo, H. A., N. M. Habran, J. A. Henao, D. F. Amado, and V. V. Kouznetsov. "Synthesis and X-ray diffraction data of 1-[N-(methyl)-(3,5-dimethylphenylamino)]methylnaphthalene." Powder Diffraction 26, no. 1 (2011): 74–77. http://dx.doi.org/10.1154/1.3540774.

Full text

Abstract:

The 1-[N-(methyl)-(3,5-dimethylphenylamino)]methylnaphthalene (chemical formula C20H21N) was prepared by means of a condensation between alpha-naphthylaldehyde and 3,5-dimethylaniline in anhydrous ethanol to obtain the aldimine (1) which was reduced with NaBH4 to afford the 1-[N-(3,5-dimethylphenylamino)]methylnaphtalene (2), and finally, the compound (3) was obtained by N-alkylation reaction of (2) with methyl iodine (CH3I) and potassium carbonate (K2CO3) in acetone. Final compound (3) was purified by chromatographic column. The XRPD pattern for the new compound, 1-[N-(methyl)-(3,5-dimethylph

APA, Harvard, Vancouver, ISO, and other styles

19

Comber, Mark F., Jonathan C. Morris, and Melvyn V. Sargent. "Synthesis of Some 1,2,3,8-Tetrasubstituted Naphthalenes." Australian Journal of Chemistry 51, no. 1 (1998): 19. http://dx.doi.org/10.1071/c97190.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Lee, Chang Ha, Dennis M. Dempsey, Rahoma S. Mohamed, and Gerald D. Holder. "Vapor-liquid equilibria in the systems of n-decane/tetralin, n-hexadecane/tetralin, n-decane/1-methylnaphthalene, and 1-methylnaphthalene/tetralin." Journal of Chemical & Engineering Data 37, no. 2 (1992): 183–86. http://dx.doi.org/10.1021/je00006a012.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Wang, Zenghui, Wenyang Fan, Dongmei Xu, et al. "Liquid–Liquid-Phase Equilibrium for Quaternary Systems (n-Decane + 1-Tetradecene + 1-Methylnaphthalene + Sulfolane/Dimethyl Sulfoxide) for Separation of 1-Methylnaphthalene from FCC Diesel." Journal of Chemical & Engineering Data 66, no. 7 (2021): 2803–11. http://dx.doi.org/10.1021/acs.jced.1c00194.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Vennila, Jasmine P., D. John Thiruvadigal, Helen P. Kavitha, G. Chakkaravarthi, and V. Manivannan. "N-[2-(3,4-Dimethoxyphenyl)ethyl]-N-methylnaphthalene-1-sulfonamide." Acta Crystallographica Section E Structure Reports Online 68, no. 3 (2012): o890. http://dx.doi.org/10.1107/s1600536812008203.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Zhang, H. Z., P. Davidovits, L. R. Williams, C. E. Kolb, and D. R. Worsnop. "Uptake of Organic Gas Phase Species by 1-Methylnaphthalene." Journal of Physical Chemistry A 109, no. 17 (2005): 3941–49. http://dx.doi.org/10.1021/jp050323n.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Xing, Shiyong, Yan Cui, Fenglin Zhang, et al. "Study of the zeolite-catalyzed isomerization of 1-methylnaphthalene." RSC Advances 14, no. 52 (2024): 38335–44. https://doi.org/10.1039/d4ra05881j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Ogata, Eisuke, Xian-Yong Wei, Kazuyuki Horie, Akio Nishijima, Ikuo Saito, and Koji Ukegawa. "Catalysis of iron sulfates on hydroconversion of 1-methylnaphthalene." Catalysis Today 43, no. 3-4 (1998): 161–69. http://dx.doi.org/10.1016/s0920-5861(98)00146-1.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Leininger, Jean-Philippe, François Lorant, Christian Minot, and Françoise Behar. "Mechanisms of 1-Methylnaphthalene Pyrolysis in a Batch Reactor." Energy & Fuels 20, no. 6 (2006): 2518–30. http://dx.doi.org/10.1021/ef0600964.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Wang, Shiyuan, Songhui Wang, Bin Wang, Zhao Jiang, and Tao Fang. "Research on Binary Phase Equilibrium for 1-Methylnaphthalene + CO2." Journal of Chemical & Engineering Data 65, no. 5 (2020): 2813–18. http://dx.doi.org/10.1021/acs.jced.0c00121.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Thiyagarajan, P., Jerry E. Hunt, Randall E. Winans, Ken B. Anderson, and Jeffrey T. Miller. "Temperature-Dependent Structural Changes of Asphaltenes in 1-Methylnaphthalene." Energy & Fuels 9, no. 5 (1995): 829–33. http://dx.doi.org/10.1021/ef00053a014.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

R., JOEL KARUNAKARAN, MATHEWS MARIAM, and GOPALAN R. "Kinetics of Iodination of Naphthalene and 1-Methylnaphthalene in presence of Nitric and Sulphuric Acids." Journal of Indian Chemical Society Vol. 68, Oct 1991 (1991): 568–69. https://doi.org/10.5281/zenodo.6154095.

Full text

Abstract:

Department of Chemistry, Madras Chritistian College, Tambatam, Madras-600 059 <em>Manuscript received 6 December 1990, revised 10 September 1991, accepted 4 October 1991</em> Kinetics of Iodination of Naphthalene and 1-Methylnaphthalene in presence of Nitric and Sulphuric Acids.

APA, Harvard, Vancouver, ISO, and other styles

30

Sun, Jingjing, Nan Zhang, Haibo Jin та ін. "The catalytic performance of acid-modified Hβ molecular sieves for environmentally friendly acylation of 2-methylnaphthalene". Green Processing and Synthesis 11, № 1 (2022): 732–46. http://dx.doi.org/10.1515/gps-2022-0067.

Full text

Abstract:

Abstract 2,6-Methylacylnaphthalene is an important organic chemical raw material, mainly used as a precursor for synthesizing polyethylene 2,6-naphthalene dicarboxylate (PEN). The heterogeneous catalyst molecular sieve catalyzes the acylation of 2-methylnaphthalene to synthesize β,β-methylacylnaphthalene, which has good activity, is green and environmentally friendly, with simple post-treatment. Different molecular sieves and reaction solvents were selected, and Hβ molecular sieves were more suitable for the acylation reaction of 2-methylnaphthalene. The reaction results were better when sulfo

APA, Harvard, Vancouver, ISO, and other styles

31

Daugé, Pierre, Antoine Baylaucq, and Christian Boned. "High-pressure viscosity behaviour of the tridecane + 1-methylnaphthalene system." High Temperatures-High Pressures 31, no. 6 (1999): 665–80. http://dx.doi.org/10.1068/htrt197.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Kukkadapu, Goutham, and Chih-Jen Sung. "Autoignition Study of 1-Methylnaphthalene in a Rapid Compression Machine." Energy & Fuels 31, no. 1 (2016): 854–66. http://dx.doi.org/10.1021/acs.energyfuels.6b01628.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Aguinaldo, AM, JA Armstrong, JR Cannon, et al. "Stoechadone: a New Naphthoquinone From Conospermum stoechadis." Australian Journal of Chemistry 49, no. 2 (1996): 197. http://dx.doi.org/10.1071/ch9960197.

Full text

Abstract:

Extraction of the dried root bark of the Western Australian plant Conospermum stoechadis Endl . has yielded 3,6,7-trimethoxy-2-methylnaphthalene-1,4-dione, stoechadone (1). The structure was elucidated by spectroscopic methods and was confirmed by a short synthesis from methyl homoveratrate (3).

APA, Harvard, Vancouver, ISO, and other styles

34

Frišták, Vladimír, Marion Graser, Martin Pipíška, Barbora Micháleková-Richveisová, and Gerhard Soja. "Pyrolysis Products as Soil Fertilizers: Screening of Potentially Hazardous Aromatic Compounds." Nova Biotechnologica et Chimica 15, no. 1 (2016): 35–46. http://dx.doi.org/10.1515/nbec-2016-0004.

Full text

Abstract:

Abstract This study investigated the concentrations of polycyclic aromatic hydrocarbons (PAHs) in pyrogenic carbonaceous materials (PCM) produced from three waste materials during slow pyrolysis at 400 and 500°C. As feedstocks bone meal (BM), biogas slurry (BC) and chicken manure (CM) were used. As potentially problematic substances 1- and 2- methylnaphthalene were analysed as indicators for methylated hydrocarbons in pyrolysis products. The phytotoxic effect of soil amendments was evaluated by a standard cress germination test with Lepidium sativum L. The analysis showed higher concentrations

APA, Harvard, Vancouver, ISO, and other styles

35

Banwell, MG, JR Dupuche, and RW Gable. "A Caveat Concerning Anionic Oxy-cope Rearrangements Within Bicyclo[2.2.2]octenyl Frameworks." Australian Journal of Chemistry 49, no. 5 (1996): 639. http://dx.doi.org/10.1071/ch9960639.

Full text

Abstract:

Compounds (10), (15) and (16) all react with potassium hydride at 0°C to give, via retro- Diels-Alder reaction, 1-methylnaphthalene (12) in 60-67% yield. No evidence could be obtained for the formation of a product derived from the anionic oxy-Cope rearrangement of substrate (16).

APA, Harvard, Vancouver, ISO, and other styles

36

Butler, Mark S., Peter L. Katavic, Paul I. Forster, and Gordon P. Guymer. "Two New Naphthoquinones from the Roots of Conospermum sphacelatum." Australian Journal of Chemistry 52, no. 8 (1999): 813. http://dx.doi.org/10.1071/ch99041.

Full text

Abstract:

Two new naphthoquinones, 8-[(2′E)-3′,7′-dimethylocta-2′,6′-dienyl]-2,7-dihydroxynaphthalene-1,4-dione (1) and 2-hydroxy-6,7-dimethoxy-3-methylnaphthalene-1,4-dione (2), and one known naphthoquinone, (+)-teretifolione-B (3), were isolated from the roots of Conospermum sphacelatum Hook. (Proteaceae) collected in central Queensland. The structures of compounds (1) and (2) were determined by spectroscopic analysis.

APA, Harvard, Vancouver, ISO, and other styles

37

Demirel, Belma, and Wendell H. Wiser. "High conversion (98%) for the hydrogenation of 1-methylnaphthalene to methyldecalins." Fuel Processing Technology 53, no. 1-2 (1997): 157–69. http://dx.doi.org/10.1016/s0378-3820(97)00044-1.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Zha, Wuyi, Depu Chen, and Weiyang Fei. "THE HPLC SEPARATION OF FULLERENES WITH 1-METHYLNAPHTHALENE MODIFIED PSDVB RESIN." Journal of Liquid Chromatography & Related Technologies 22, no. 16 (1999): 2443–53. http://dx.doi.org/10.1081/jlc-100101813.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

MURATA, YOSHIAKI, AYUMI DENDA, HIROSHI MARUYAMA, and YOICHI KONISHI. "Chronic Toxicity and Carcinogenicity Studies of 1-Methylnaphthalene in B6C3F1 Mice." Toxicological Sciences 21, no. 1 (1993): 44–51. http://dx.doi.org/10.1093/toxsci/21.1.44.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Baylaucq, A., P. Daugé, and C. Boned. "Viscosity and density of the ternary mixture heptane+methylcyclohexane+1-methylnaphthalene." International Journal of Thermophysics 18, no. 5 (1997): 1089–107. http://dx.doi.org/10.1007/bf02575251.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Bounaceur, Roda, Jean-Philippe Leininger, François Lorant, Paul-Marie Marquaire, and Valérie Burklé-Vitzthum. "Kinetic modeling of 1-methylnaphthalene pyrolysis at high pressure (100 bar)." Journal of Analytical and Applied Pyrolysis 124 (March 2017): 542–62. http://dx.doi.org/10.1016/j.jaap.2017.01.027.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Drozdowski, H. "X-ray Analysis of Liquid 1-Methylnaphthalene Structure at 293 K." Acta Physica Polonica A 98, no. 6 (2000): 691–703. http://dx.doi.org/10.12693/aphyspola.98.691.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Jaroszewska, K., A. Masalska, J. R. Grzechowiak, and J. Grams. "Hydroconversion of 1-methylnaphthalene over Pt/AlSBA-15–Al2O3 composite catalysts." Applied Catalysis A: General 505 (September 2015): 116–30. http://dx.doi.org/10.1016/j.apcata.2015.07.021.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Chae, Myung-Soo, Sung-Geun Woo, Jae-Kyu Yang, Sei-Dal Bae, and Sang-Il Choi. "Treatability Evaluation of N-Hexadecane and 1-Methylnaphthalene during Fenton Reaction." Environmental Engineering Research 17, no. 4 (2012): 217–25. http://dx.doi.org/10.4491/eer.2012.17.4.217.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Takagi, Yoshinori, Tatsuya Nobusawa, and Toshihide Suzuki. "Prevention and Estimation of Catalytic Deactivation in Isomerization of 1-Methylnaphthalene." KAGAKU KOGAKU RONBUNSHU 21, no. 6 (1995): 1096–103. http://dx.doi.org/10.1252/kakoronbunshu.21.1096.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Ferino, I., R. Monaci, E. Rombi, and V. Solinas. "Microcalorimetric investigation of mordenite and Y zeolites for 1-methylnaphthalene isomerisation." Journal of the Chemical Society, Faraday Transactions 94, no. 17 (1998): 2647–52. http://dx.doi.org/10.1039/a803931c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Murata, Y. "Chronic Toxicity and Carcinogenicity Studies of 1-Methylnaphthalene in B6C3F1 Mice." Fundamental and Applied Toxicology 21, no. 1 (1993): 44–51. http://dx.doi.org/10.1006/faat.1993.1070.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Kim, Yong-Soon, Mi-Ju Lee, Dong-Suk Seo, Tae-Hyun Kim, Min-Ha Kim, and Cheol-Hong Lim. "Thirteen-week inhalation toxicity study of 1-methylnaphthalene in F344 rats." Toxicological Research 36, no. 1 (2019): 13–20. http://dx.doi.org/10.1007/s43188-019-00009-1.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Kim, Su Jin. "Study on Removal of Nitrogen-Containing Heterocyclic Compounds Contained in Crude Methylnaphthalene Oil by Formamide Extraction." Processes 12, no. 8 (2024): 1550. http://dx.doi.org/10.3390/pr12081550.

Full text

Abstract:

This study examined the effect of experimental factors and conditions on the removal of nitrogen-containing heterocyclic compounds (NCHCs) by performing equilibrium extraction using formamide or formamide aqueous solution as a solvent to remove NCHCs contained in crude methylnaphthalene oil (CMNO). The CMNO used as a raw material in this study contained three types of NCHCs (quinoline, isoquinoline, and indole) classified as group A, and six kinds of non-NCHCs (naphthalene, 1-methylnaphthalene, 2-methylnaphthalene, biphenyl, dibenzofuran, and fluorene) classified as group B. Increasing the vol

APA, Harvard, Vancouver, ISO, and other styles

50

Yue, Xiao Ming, Bing Sun, Zhi Min Zong, Yao Lu, Li Min Mei, and Xian Yong Wei. "Hydrocracking of Di(1-Naphthyl)methane over Acid Solid Catalyst." Advanced Materials Research 236-238 (May 2011): 850–53. http://dx.doi.org/10.4028/www.scientific.net/amr.236-238.850.

Full text

Abstract:

As a model reaction for coal liquefaction, the hydrocraking of di(1-naphthyl)methane (DNM) was investigated using acid solid catalyst (ASC) under different reaction conditions. The results show that acid solid catalyst selectively catalyzes DNM hydrocraking to give 1-methylnaphthalene and naphthalene, without hydrogenation product. The rate of DNM hydrocraking strongly depended on reaction temperature, reaction time and the catalyst feed, whereas effect of hydrogen pressure was not serious. The effects of acid solid catalyst is to make Car-Calk bond cleavage.

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!