Relevant bibliographies by topics / Naphthalene

Contents

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

Academic literature on the topic 'Naphthalene'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Naphthalene"

1

Halton, Brian, Carissa S. Jones, Peter T. Northcote, and Roland Boese. "Studies in the Cycloproparene Series: Formation of a New Dimer of 1H-Cyclopropa[b]naphthalene." Australian Journal of Chemistry 52, no. 4 (1999): 285. http://dx.doi.org/10.1071/c98179.

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1-(Trimethylsilyl)-1H-cyclopropa[b]naphthalene (10) and its 1-methyl derivative (11) have been isolated as pure compounds from use of a lipophilic size exclusion gel. Acylation of the 1H-cyclopropa[b]naphthalenyl anion (2) is effected with N,N -dimethyl-benzamide and -acetamide to give (5) and (6), respectively. Analogous reactions with the 1-(trimethylsilyl)-1H-cyclopropa[b]naphthalenyl anion (9) do not yield the 1-acyl-1-(trimethylsilyl)-1H-cyclopropa[b]naphthalenes (12) and (13); instead the novel 6-methyl- 7H-dibenzo[b,g]fluorene (15) results from attempted acetylation. Compound (15), a fo
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Hernández-Téllez, Guadalupe, Gloria E. Moreno, Sylvain Bernès, et al. "Crystal structures of ten enantiopure Schiff bases bearing a naphthyl group." Acta Crystallographica Section E Crystallographic Communications 72, no. 4 (2016): 583–89. http://dx.doi.org/10.1107/s2056989016004692.

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Using a general solvent-free procedure for the synthesis of chiral Schiff bases, the following compounds were synthesized and their crystal structures determined: (S)-(+)-2-{[(1-phenylethyl)imino]methyl}naphthalene, C19H17N, (1), (S)-(+)-2-({[(4-methylphenyl)ethyl]imino}methyl)naphthalene, C20H19N, (2), (R)-(−)-2-({[(4-methoxylphenyl)ethyl]imino}methyl)naphthalene, C20H19NO, (3), (R)-(−)-2-({[(4-fluorophenyl)ethyl]imino}methyl)naphthalene, C19H16FN, (4), (S)-(+)-2-({[(4-chlorophenyl)ethyl]imino}methyl)naphthalene, C19H16ClN, (5), (S)-(+)-2-({[(4-bromophenyl)ethyl]imino}methyl)naphthalene, C19H
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Ansink, Harold R. W., Erik J. De Graaf, Erwin Zelvelder, and Hans Cerfontain. "Reactions of SO2X mono-substituted arenes with SO3 in nitromethane: electronic and steric directing effects of the sulfonic acid group and some model substituents." Canadian Journal of Chemistry 71, no. 2 (1993): 210–15. http://dx.doi.org/10.1139/v93-031.

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The sulfonation of benzene-SO2X (X = CH3, OCH3, OH, and Cl) and of 1- and 2-naphthalene-SO2X (X = CH3, OCH3, and Cl) with sulfur trioxide in nitromethane as solvent has been studied. In the benzene series, substitution only occurs at the 3-position irrespective of X; the reaction rates, which are all within the same order of magnitude, are low. Upon sulfonation of the 1-SO2X-substituted naphthalenes, the main sulfonation product (58–80%) is the 5-sulfonic acid (5-S); in addition, 6-S and small amounts of 3-S and 7-S are formed. Also, the formation of the intermolecular sulfonic anhydride of 1-
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El-Dossoki, Farid I. "Protonation and Solvation Thermodynamics of Some Naphthol Derivatives in KCl Aqueous Solution of Different Ionic Strengths." Journal of Chemistry 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/7234320.

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The acid-base properties of naphthalen-1-ol (L1), naphthalene-1,5-diol (L2), and 4-amino-3-hydroxynaphthalene-1-sulphonic acid (L3) were characterized from pH-metric measurements in pure water and in different concentrations (0–4 mol kg−1) of aqueous KCl solutions at the temperature range ofT= (293.15 to 213.15) K at 5 K intervals. The results reveal that naphthalen-1-ol and naphthalene-1,5-diol molecules have two ionisable protons (of the hydroxyl groups) while 4-amino-3-hydroxynaphthalene-1-sulphonic acid has three ionisable protons (hydrogen ion of the hydroxyl group, SO3H, andNH3+). Modeli
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Ibrahim, Mohamed N., Salaheddin A. I. Sharif, Ahmad N. EL-Tajory, and Asma A. Elamari. "Synthesis and Antibacterial Activities of Some Schiff Bases." E-Journal of Chemistry 8, no. 1 (2011): 212–16. http://dx.doi.org/10.1155/2011/258340.

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Schiff basesp-hydroxybenzylidene-2-carboxyaniline,p-nitrobenz-ylidene-2-carboxyaniline,p-(N, N-dimethyl)aminobenzylidene-2-carboxyaniline,N-(4-hydroxybezylidene)-benzene-1,2-diamine,N--(4-nitrobezylidene)benzene-1,2-diamine,N-(4-(N, N-dimethylaminobezylidene)benzene-1,2-diamine,N-(4-(N,N-dimethylamino)benzylidene)naphthalen-1-amine,N-(4-nitrobenzylidene)naphthalen-1-amine,N--(4-chlorobenzylidene)naphthalen-1-amine,sodium-4-(4-(N,N-dimethyl amino)benzylideneamino)naphthalene-1-sulfonate,sodium -4-(4-nitrobenzylidene-amino)naphthalene-1-sulfonate and sodium-4-(4-chlorobenzylideneamino) naphthale
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Xu, Peng, Wencheng Ma, Hongjun Han, Baolin Hou, and Shengyong Jia. "Characterization of naphthalene degradation by Streptomyces sp. QWE-5 isolated from active sludge." Water Science and Technology 70, no. 6 (2014): 1129–34. http://dx.doi.org/10.2166/wst.2014.356.

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A bacterial strain, QWE-5, which utilized naphthalene as its sole carbon and energy source, was isolated and identified as Streptomyces sp. It was a Gram-positive, spore-forming bacterium with a flagellum, with whole, smooth, convex and wet colonies. The optimal temperature and pH for QWE-5 were 35 °C and 7.0, respectively. The QWE-5 strain was capable of completely degrading naphthalene at a concentration as high as 100 mg/L. At initial naphthalene concentrations of 10, 20, 50, 80 and 100 mg/L, complete degradation was achieved within 32, 56, 96, 120 and 144 h, respectively. Kinetics of napht
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Zhang, Ru Ling. "Study on Pollution Level, Distribution and Sources of Polychlorinated Naphthalene in River Sediments." Applied Mechanics and Materials 686 (October 2014): 689–94. http://dx.doi.org/10.4028/www.scientific.net/amm.686.689.

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Polychlorinated naphthalene (PCNs) is similar structure and toxicity of dioxin (PCDD/Fs), it can be detected in the global environmental and biological samples. This paper introduces the main source of PCNs in the environment and environmental fate, sludge PCNs pollution level in 1.48~28.21 ng/g (dry weight), PCN-TEQs content is in 0.11~2.45 pg/g (dry weight), far below the content of other areas in foreign countries. The results showed that the sources of wastewater, sewage treatment plant is an important factor affecting the level of polychlorinated naphthalene pollution. Discussion on the d
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Gallucci, J. C., D. J. Hart, and D. G. J. Young. "Nucleophile–Electrophile Interactions in 1,8-Disubstituted Naphthalenes: Structures of Three 1-Naphthaldehydes and a 1-Naphthyl Methyl Ketone." Acta Crystallographica Section B Structural Science 54, no. 1 (1998): 73–81. http://dx.doi.org/10.1107/s0108768197009440.

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4,8-Dimethoxy-5-(tosyloxy)-1-naphthaldehyde (1) and 8-methoxy-5-(tosyloxy)-1-naphthaldehyde (2) crystallize such that the formyl groups approach coplanarity with the naphthalene rings. 4′,8′-Dimethoxy-5′-(tosyloxy)-1′-acetonaphthone (4), however, crystallizes such that the acetyl group approaches orthogonality to the naphthalene ring. In all three compounds the methoxy group and carbonyl groups exhibit a leaning effect typical of nucleophile–electrophile interactions in 1,8-disubstituted naphthalenes. 8-(Benzoyloxy)-4-methoxy-1-naphthaldehyde (3) crystallizes with the formyl group nearly copla
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Schmidbaur, H., W. Bublak, and G. Müller. "Cyclophan-Metall-Komplexe: Synthese und Kristallstruktur von ([2](l,4)Naphthalino[2]paracyclophan)gallium(I)-tetrabromogallat(III)/Cyclophane Metal Complexes: Synthesis and Crystal Structure of ([2]( 1,4)Naphthalino[2]paracyclophane)gallium(I) Tetrabromogallate(III)." Zeitschrift für Naturforschung B 42, no. 2 (1987): 147–50. http://dx.doi.org/10.1515/znb-1987-0205.

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AbstractThe title complex has been prepared from Ga[GaBr4] and [2](1,4)naphthalino[2]paracyclophane in toluene as a solvent, and the crystal structure of this adduct determined by single crystal X-ray diffraction. The structure is composed of dimeric units Ga2[GaBr4]2 , which are crosslinked into sheets through Ga(I)-arene coordination. Both the benzene ring and the substituted ring of the naphthalene system are η6-bonded from the outer side of the cyclophane cage, each to an univalent metal. The benzene and the naphthalene form an interplane angle of 49.3°. The distance to the benzene ring (2
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Tummala, Manorama, Raj K. Dhar, Frank R. Fronczek, and Steven F. Watkins. "1-[3-(Naphthalen-1-yl)phenyl]naphthalene." Acta Crystallographica Section E Structure Reports Online 69, no. 2 (2013): o307. http://dx.doi.org/10.1107/s1600536813002407.

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The title compound, C26H18, consists of a benzene ring withmeta-substituted 1-naphthalene substituents, which are essentially planar (r.m.s. deviation = 0.039 and 0.027 Å). The conformation is mixedsyn/anti, with equivalent torsion angles about the benzene–naphthalene bonds of 121.46 (11) and 51.58 (14)°.
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Dissertations / Theses on the topic "Naphthalene"

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Hibbeln, Kim Sabine. "Effect of kaolinite and cadmium on the biodegradation of naphthalene and substituted naphthalenes." Thesis, McGill University, 1996. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=24011.

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The objectives of this study were to look at the effect of kaolinite and cadmium on the biodegradation of naphthalene and substituted naphthalenes. The kaolinite mineral is present in many Quebec soils and is a primary constituent of tropical soils. Since kaolinite is also a well defined mineral, experiments were performed to examine the effect kaolinite might play on the degradation of naphthalene, 2-methyl naphthalene, and 2-naphthol in the presence and absence of cadmium. Furthermore, the results from these analyses were used to interpret the behaviour in the mineralization experiments of e
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Quinn, Samuel. "Colouring naphthalene diimides." Thesis, University of Nottingham, 2018. http://eprints.nottingham.ac.uk/50038/.

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Naphthalene diimides have been explored in a wide variety of ways; They are a promising candidate for organic electronics, boasting the ability to form n-type semiconductor materials, the stability of their anions further aiding in this regard. Their electron poor aromatic core can be used in host guest chemistry to generate interlocked species. The ability to tune their electronic properties and how this could be manipulated to create photovoltaic devices is primarily focus of this thesis. A series of naphthalene diimides substituted at the core with morpholine moieties have been synthesized
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Nehls, Benjamin S. "Naphthalene based conjugated materials." [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=976731363.

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Kim, Michelle B. "The Hydrolysis of Naphthalene Diimides." Digital Archive @ GSU, 2007. http://digitalarchive.gsu.edu/chemistry_theses/7.

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The hydrolyses of naphthalene diimides (NDIs) bearing aliphatic side chains with N-methylpyrrolidinium groups placed two (1) and three (5) atoms from the central core were studied. The Ka values for the first and second hydrolyses for 1 were 2.5 ± 0.2 x 105 M-1 and 2.0 ± 0.1 x 102 M-1, respectively; for 5 they were 1.4 ± 0.1 x 105 M-1 and 44 ± 2 M-1, respectively. NDI 1 hydrolyzed 6.8 times faster than did 5. The rates for the first and second hydrolyses of 1 at 100 mM hydroxide measured by stopped-flow were 17.0 ± 0.2 s-1 and 53.0 ± 0.1 x 10-2 s-1, respectively. NMR showed both the syn and an
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Gubellini, Federico. "Designing heterogeneous catalysts for naphthalene isopropylation." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2020. http://amslaurea.unibo.it/20659/.

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2,6 di-isopropylnaphthalene is a plant growth regulator and it is used for the manufacturing of products intended to prevent sprouting of stored potatoes; despite that in the last decades it has been mainly produced as a precursor of the corresponding dicarboxylic acid (2,6-naphthalene dicarboxylic acid) which is, with ethylene glycol, the monomer for polyethylene naphthalate (PEN) polymerization. PEN results appealing for many uses for which PET is more commonly utilized; the most relevant, higher glass transition temperature (PEN 122°C, PET 80°C), higher Young’s modulus (PEN 5200 MPa, PET 3
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Bakker, M. G. "ESR studies on some naphthalene derivatives." Thesis, University of Canterbury. Chemistry, 1985. http://hdl.handle.net/10092/8639.

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ESR Spectroscopy has been used to study conformational interconversion and addivity relationships in a number of series of naphthalene derivatives. Oscillation of the alkyl rings in 1,2,3,6,7,8-hexahydropyrene ions, and the ions of the related 5, 6 and 7 membered ring compounds has been studied. The temperature dependance of the ESR spectra have been used to assign the coupling constants. The aromatic ring coupling constants in the asymmetric compounds have been assigned on the basis of an additivity relationship. The ESR spectra of a number of methylnaphthalene anions have been recorded and
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黃文菁 and Man-ching Wong. "Synthesis of the naturally occurring 1, 2-naphthalenedione, azanzoneA." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1993. http://hub.hku.hk/bib/B31211033.

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Wong, Man-ching. "Synthesis of the naturally occurring 1, 2-naphthalenedione, azanzone A /." [Hong Kong : University of Hong Kong], 1993. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13457093.

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Carey, Michelle Jocelyn. "The photophysics of naphthalene containing synthetic polymers." Thesis, Imperial College London, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320273.

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Senior, Kerry Charles. "Biotreatment of industrial effluents containing naphthalene sulphonate." Thesis, University of Kent, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.270819.

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Books on the topic "Naphthalene"

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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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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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United States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Naftalina, 1-metilnaftalina y 2-metilnaftalina. Agencia para Sustancias Tóxicas y el Registro de Enfermedades, División de la Toxicología, Departamento de Salud y Servicios Humanos de los EE.UU., Servicio de Salud Pública, 2005.

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Antsyforov, Gleb I., and Alyona F. Ivanski. Napthalene: Structure, properties, and applications. Nova Science Publishers, 2011.

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D, Nitterauer James, and United States. Environmental Protection Agency, eds. Biotransformation of benzothiophene by isopropylbenzene-degrading bacteria. Environmental Protection Agency], 1994.

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Nii͡azov, A. N. Naftenaty. Ylym, 1992.

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United States. Environmental Protection Agency. Emissions Standards and Engineering Division. and United States. Environmental Protection Agency. Office of Air Quality Planning and Standards., eds. Summary of emissions associated with sources of naphthalene. U.S. Environmental Protection Agency, 1986.

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Kreutz, Martin. Halogen-Metall-Austausch bei Bromnaphthalinen: Synthese, Struktur, und Reaktionsweisen mono- und polylithiierter Naphthaline. A.S. Intemann, 1991.

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Humans, IARC Working Group on the Evaluation of Carcinogenic Risks to. Some traditional herbal medicines, some mycotoxins, naphthalene and styrene. IARC Press, 2002.

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Derner, Harald. Untersuchungen über den Resonanz-Ramaneffekt an Anthracen, Naphthalin und p-nitro-p-dimethylamino-azobenzol. Hochschulverlag, 1986.

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Book chapters on the topic "Naphthalene"

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Capinera, John L., Marjorie A. Hoy, Paul W. Paré, et al. "Naphthalene." In Encyclopedia of Entomology. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_2142.

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Bailey, Lisa A., Laura E. Kerper, and Lorenz R. Rhomberg. "Naphthalene." In Hamilton & Hardy's Industrial Toxicology. John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781118834015.ch65.

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Gooch, Jan W. "Naphthalene." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_7776.

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Lide, David R. "Naphthalene." In Handbook of Organic Solvents. CRC Press, 2024. http://dx.doi.org/10.1201/9781003575191-358.

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Bährle-Rapp, Marina. "Dibenzoxazoyl Naphthalene." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2867.

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Turhan, Munire. "Moisture, Electrical Conductivity, Water-Insoluble Solid Matter, Free Acidity and Ph Analysis Methods in Honey." In Methods of Biochemical Analysis of Bee Products. Nobel Tip Kitabevleri, 2024. http://dx.doi.org/10.69860/nobel.9786053359326.2.

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Honey is a very important natural food consumed as a source of healing. However, it can become harmful due to different chemicals mixed into the content of honey. Naphthalene is a carcinogenic hydrocarbon compound that forms residues in honey. Naphthalene, which beekeepers use to prevent honeycombs from mothballing but are prohibited from using, has many harmful effects on health. The Turkish Food Codex Honey Communiqué states that naphthalene in honey can be at a maximum concentration of 10 µm/kg. Many international organizations and states have set this limit. Therefore, naphthalene analysis
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Izol, Ebubekir. "Naphthalene Analysis in Honey by Gas Chromatography Technology." In Methods of Biochemical Analysis of Bee Products. Nobel Tip Kitabevleri, 2024. http://dx.doi.org/10.69860/nobel.9786053359326.1.

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Honey is a very important natural food consumed as a source of healing. However, it can become harmful due to different chemicals mixed into the content of honey. Naphthalene is a carcinogenic hydrocarbon compound that forms residues in honey. Naphthalene, which beekeepers use to prevent honeycombs from mothballing but are prohibited from using, has many harmful effects on health. The Turkish Food Codex Honey Communiqué states that naphthalene in honey can be at a maximum concentration of 10 µm/kg. Many international organizations and states have set this limit. Therefore, naphthalene analysis
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Schomburg, Dietmar, and Dörte Stephan. "Naphthalene 1,2-dioxygenase." In Enzyme Handbook. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-57942-4_81.

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Wohlfarth, Ch. "Viscosity of naphthalene." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_335.

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Wohlfarth, Ch. "Dielectric constant of naphthalene." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_288.

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Conference papers on the topic "Naphthalene"

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Jia, Dan, Huimin Liu, and Dongyan Gu. "Preparation of Naphthalene Molecularly Imprinted Absorbent and its adsorption for Naphthalene." In 2017 3rd International Forum on Energy, Environment Science and Materials (IFEESM 2017). Atlantis Press, 2018. http://dx.doi.org/10.2991/ifeesm-17.2018.288.

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Melker, Alexander I., Dimitri A. Kornilov, Tatiana V. Vorobyeva, and Denis Kalinin. "Conformational transitions in naphthalene." In SPIE Proceedings, edited by Alexander I. Melker. SPIE, 2004. http://dx.doi.org/10.1117/12.555442.

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Junbiao Peng, Runguang Son, Yuguang Ma, Haifeng Zhang, and Shiyong Liu. "Electroluminescent of plasma polymerized naphthalene." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835421.

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Ciocci, Richard C. "Characterizing Naphthalene via Material Flow Analysis." In ASME 2005 International Mechanical Engineering Congress and Exposition. ASMEDC, 2005. http://dx.doi.org/10.1115/imece2005-82808.

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An Environmental Protection Agency-funded project centers on the material flow analysis of naphthalene-containing products in an effort to eliminate, reduce, or replace the sources of naphthalene. The analysis commences with manufacturers who use naphthalene-containing products in their processes. Also, the analysis works in reverse by starting with the naphthalene user, as the material will be traced to the source in an effort to identify elimination/reduction opportunities throughout the material’s life cycle. A particular focus is the potential for removal of naphthalene from the primary pr
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Hill, Jeffrey R., and Dana D. Dlott. "Vibrational Relaxation and Energy Transfer in Ordered and Disordered Molecular Crystals." In International Conference on Ultrafast Phenomena. Optica Publishing Group, 1986. http://dx.doi.org/10.1364/up.1986.tuf2.

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Vibrational energy transfer in condensed phases is a process which occurs on the picosecond time scale. In our lab, we are studying this process in complex molecules in the well-defined environment of a single molecular crystal. We have measured the lifetime of several vibrons in the model system naphthalene, and then extended these studies to several partially deuterated naphthalenes [1,2]. Vibrations in pure crystals form delocalized vibron bands which relax by emission of optical phonons. In disordered or mixed crystals, excited vibrations scatter off impurities and transfer energy to adjac
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Ciocci, Richard, Daniel Massey, and Steve Funck. "Developing a Process to Identify Material Flow of a Priority Chemical." In ASME 2006 International Mechanical Engineering Congress and Exposition. ASMEDC, 2006. http://dx.doi.org/10.1115/imece2006-13727.

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An Environmental Protection Agency-funded project was the material flow analysis of naphthalene-containing products in an effort to eliminate, reduce, or replace the sources of naphthalene. The project analysis began with manufacturers who use naphthalene-containing products in their processes. It identifies the basic characteristics of naphthalene as a common polynuclear aromatic hydrocarbon, which is released to the environment. Included are likely sources of naphthalene emissions and releases as they were identified for further investigation. This paper, which is the sequel to IMECE 2005-82
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Nikulina, N., Sergey Nikulin, and A. Dmitrenkov. "PRODUCTION OF MODIFIED WOOD USING VINYL NAPHTHALENE DERIVATIVE." In ENERGY-SAVING AND ENVIRONMENTALLY SAFE TECHNOLOGIES OF THE TIMBER INDUSTRY – 2025. FSBE Institution of Higher Education Voronezh State University of Forestry and Technologies named after G.F. Morozov, 2025. https://doi.org/10.58168/e-sestti2025_284-288.

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The compositions for processing natural birch wood, obtained on the basis of ethenyl derivatives of naphthalene, are investigated in the work. A solution of naphthalene derivatives in toluene with additives of pinane hydroperoxide was used for wood processing. The removal of toluene from modified timber samples was combined with radical polymerization of ethenyl naphthalene derivatives in an autoclave at 160-165 0C for 5 hours. The polymer content in the timber varied from 10 to 26%. Manufactured timber products containing ethenyl naphthalene derivatives will provide products based on them not
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Wijenayake, U., A. Kumara, S. Langappuli, and J. Samaranayake. "Enhancing the Performance of Petroleum Bitumen 60/70 through Modification with Crude Naphthalene." In 5th International Conference on Advances in Highway Engineering & Transportation Systems 2024, edited by H. R. Pasindu. Transport Engineering Division, Department of Civil Engineering, University of Moratuwa, 2024. https://doi.org/10.31705/icahets.2024.5.

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Abstract:
Bitumen, a viscous mixture of hydrocarbons, is a key substance in the asphalt mixtures due to its binding and heating qualities. Most common challenges in asphalt pavements such as rutting, cracking, and deformation at moderate to high temperatures persist in asphalt pavements, necessitating the to enhance performance of bitumen. Modification of 60/70 penetration grade bitumen, by adding naphthalene was studied to mitigate the distresses appear on local road surfaces; mainly age hardening cracks and plastic deformations. As a modifier, Naphthalene is a polycyclic aromatic hydrocarbon, is intro
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Song, Fu, Yifei Shi, Shiru Jia, Zhilei Tan, and Huabing Zhao. "Advances of naphthalene degradation in Pseudomonas putida ND6." In ADVANCES IN ENERGY SCIENCE AND ENVIRONMENT ENGINEERING II: Proceedings of 2nd International Workshop on Advances in Energy Science and Environment Engineering (AESEE 2018). Author(s), 2018. http://dx.doi.org/10.1063/1.5029792.

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Dixon, D., W. Wilson, V. Steullet, and S. Takenaka. "Studies of Naphthalene Diimides as DNA-binding Agents." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02060.

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Reports on the topic "Naphthalene"

1

Buchholz, Bruce A. Mechanism for Clastogenic Activity of Naphthalene. Office of Scientific and Technical Information (OSTI), 2015. http://dx.doi.org/10.2172/1226965.

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Buchholz, Bruce A. Mechanism for Clastogenic Activity of Naphthalene. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1281678.

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Buchholz, Bruce A. Metabolic Mechanisms of Naphthalene Toxicity in Lung. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1529177.

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Kwong, C. D. Synthesis of a naphthalene-hydroxynaphthalene polymer model compound. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/7149929.

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Kwong, C. D. Synthesis of a naphthalene-hydroxynaphthalene polymer model compound. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/6884708.

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Kwong, C. D. Synthesis of a naphthalene-hydroxynaphthalene polymer model compound. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/6929711.

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Kwong, C. D. Synthesis of a naphthalene-hydroxynaphthalene polymer model compound. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/6986489.

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Ghoshal, S., A. Ramaswami, and R. G. Luthy. Biodegradation of naphthalene from coal tar. Research progress report. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10178125.

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Buchholz, B. A. Mechanism for Clastogenic Activity of Naphthalene. Quarterly Technical Progress Report. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1239176.

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Chirico, R. D., S. E. Knipmeyer, A. Nguyen, and W. V. Steele. The thermodynamic properties to 700 K of naphthalene and 2,7-dimethylnaphthalene. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10181459.

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