Relevant bibliographies by topics / Alkanol

Contents

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

Academic literature on the topic 'Alkanol'

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

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Journal articles on the topic "Alkanol"

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Ives, H. E., and A. S. Verkman. "Effects of membrane fluidizing agents on renal brush border proton permeability." American Journal of Physiology-Renal Physiology 249, no. 6 (1985): F933—F940. http://dx.doi.org/10.1152/ajprenal.1985.249.6.f933.

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H+ permeability (PH) of brush border membrane vesicles isolated from rabbit renal cortex was measured from the rate of collapse of preformed pH gradients using acridine orange fluorescence quenching. n-Alkanols increased PH from 0.005 to 0.1 cm/s in a dose-dependent manner. At 25 degrees C, PH increased to 0.01 cm/s at [n-alkanol] = 90 mM (butanol), 30 mM (pentanol), 7 mM (hexanol), and 1.8 mM (heptanol). Activation energy (Ea) of PH was 21.6 kcal/mol (5-50 degrees C), which decreased to 18.5 kcal/mol in the presence of either 200 mM butanol or 12 mM hexanol. Membrane fluidity was estimated fr
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Koch, Daniel J., Mike M. Chen, Jan B. van Beilen, and Frances H. Arnold. "In Vivo Evolution of Butane Oxidation by Terminal Alkane Hydroxylases AlkB and CYP153A6." Applied and Environmental Microbiology 75, no. 2 (2008): 337–44. http://dx.doi.org/10.1128/aem.01758-08.

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ABSTRACT Enzymes of the AlkB and CYP153 families catalyze the first step in the catabolism of medium-chain-length alkanes, selective oxidation of the alkane to the 1-alkanol, and enable their host organisms to utilize alkanes as carbon sources. Small, gaseous alkanes, however, are converted to alkanols by evolutionarily unrelated methane monooxygenases. Propane and butane can be oxidized by CYP enzymes engineered in the laboratory, but these produce predominantly the 2-alkanols. Here we report the in vivo-directed evolution of two medium-chain-length terminal alkane hydroxylases, the integral
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González, Juan Antonio, I. García De La Fuente, and J. C. Cobos. "Thermodynamics of mixtures containing the CO and OH groups. II. DISQUAC predictions on VLE and HE for ternary mixtures containing 1-alkanols, n-alkanones, and one organic solvent." Canadian Journal of Chemistry 75, no. 10 (1997): 1424–33. http://dx.doi.org/10.1139/v97-171.

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Thermodynamic properties: vapour–liquid equilibria, VLE, or excess enthalpies, HE, for a set of 21 ternary mixtures of the type 1-alkanol + n-alkanone + organic solvent are studied in the framework of the DISQUAC group contribution model. This treatment is extended to the binaries involved. The DISQUAC analysis is developed on the basis of binary interactions only, that is, ternary interactions are neglected. Most of the interchange coefficients needed are available in the literature. The average relative standard deviations are 0.026 for pressure in the VLE (12 systems) and 0.098 in the HE (9
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Bhagat, Payal, and Sanjeev Maken. "Study of Intermolecular Interactions of Binary Mixture of sec- and tert-Amines with Alkanols (C1-C3): Refractive Indices." Asian Journal of Chemistry 32, no. 10 (2020): 2443–49. http://dx.doi.org/10.14233/ajchem.2020.22719.

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In this work, the refractive indices (nD) of binary mixture of diisopropylamine (DIPA) and tributylamine (TBA) (as sec- and tert-amines) with alkanol (methanol, ethanol, 1-propanol, 2-propanol) were measured from 298.15 K to 318.15 K. The sec- and tert-amines were selected to study the effect of branching at N-atom of amine on intermolecular interactions with alkanols having different chain length. It was found that the TBA interacts strongly with alkanol in comparison to DIPA due to steric hindrance offered by isopropyl group at N-atom. Various mixing rules were applied to evaluate the refrac
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Jetter, Reinhard, and Markus Riederer. "Cuticular waxes from the leaves and fruit capsules of eight Papaveraceae species." Canadian Journal of Botany 74, no. 3 (1996): 419–30. http://dx.doi.org/10.1139/b96-052.

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Cuticular waxes from leaves and fruit capsules of Papaver alpinum sensu Markgr., P. bracteatum Lindl., P. dubium L., P. nudicaule L., P. orientale L., P. rhoeas L., P. somniferum L., and Eschscholtzia californica Cham. were investigated. They consisted of n-alkanes (< 19%), alk-1-ylesters (< 18%), alk-2-ylesters (< 6%), alkanals (< 19%), secondary alkanols (21–71%, mainly nonacosan-10-ol), triglycerides (< 6%), primary alkanols (2–33%), alkanediols (2–23%, mainly isomeric nonacosanediols), alkanoic acids (< 8%), and alkaloids (< 12%). In addition, minor amounts of iso- and
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Bui, Huong Thi. "\(\textit{n}\)-alkanol stress-induced cell envelope injury of \(σ^{E}\) promoter in \(\textit{Escherichia coli}\)". Academia Journal of Biology 44, № 2 (2022): 91–104. http://dx.doi.org/10.15625/2615-9023/17136.

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To characterize the cellular stress by n-alkanols with different alkyl chain lengths in Escherichia coli, we investigated how n-alkanols damage cell envelope permeability and whether they enhance the promoter activity of the envelope stress response regulator, σE, by using variants of green fluorescent protein (GFP). By using E. coli cells having GFPuv expressing and localizing in the cytoplasm, the inner membrane, and the periplasm, after exposure to n-alkanols, the fluorescent intensity of GFPuv released from cells was examined. Our data showed that at the similar levels of cell death of abo
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Ortega, J., JA Pena, and MI Pazandrade. "Excess Molar Volumes of Binary Mixtures of Ethyl Acetate and Propyl Acetate With Normal Alkanols." Australian Journal of Chemistry 39, no. 10 (1986): 1685. http://dx.doi.org/10.1071/ch9861685.

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This article reports measurements of VE/m at 298.15 K for binary mixtures of n- alkanols CnH2n+1OH (from n = 2 to n = 10) with ethyl and propyl acetates. All the excess volumes are positive over the entire concentration range, with VE/m increasing with the length of the alkanol chain. Suitable equations have been fitted to the data for each mixture. The results are compared with data previously published.
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Wolf, Jeremy R. "Main Chain Noncentrosymmetric Hydrogen Bonded Macromolecules Incorporating Aniline, Alkanol, and Alkanoic Acid Hydrogen Bond Donors." Journal of Polymers 2014 (April 27, 2014): 1–7. http://dx.doi.org/10.1155/2014/472901.

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The syntheses and characterization of three noncentrosymmetric main chain hydrogen bonded macromolecules which incorporate aniline, alkanoic acid, and alkanol hydrogen bond donor units are reported. These macromolecules participate in weak intermolecular hydrogen bonding as demonstrated using attenuated total reflectance (ATR) FTIR. The phase transitions of these macromolecules depend on the identity of the hydrogen bond donor.
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Piekarski, Henryk, and Gus Somsen. "Enthalpies of solution of urea in water–alkanol mixtures and the enthalpic pair interaction coefficients of urea and several nonelectrolytes in water." Canadian Journal of Chemistry 64, no. 9 (1986): 1721–24. http://dx.doi.org/10.1139/v86-284.

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Enthalpies of solution of urea in binary mixtures of isopropanol, s-butanol, and ethoxyethanol with water have been measured at high water content. Those in the binaries isopropanol + water and ethoxyethanol + water show endothermic maxima at 8 and 4 mol% alkanol, respectively. Enthalpic pair interaction coefficients are calculated for the interactions between urea and the alkanols and discussed in connection with these coefficients for interactions between urea and other nonelectrolytes and between N,N-dimethylformamide and several nonelectrolytes. The enthalpic pair interaction coefficients
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Munk, Petr, Anwei Qin, and Dolly E. Hoffman. "Excess Volumes of Mixtures of Alkanols with Aromatic Hydrocarbons." Collection of Czechoslovak Chemical Communications 58, no. 11 (1993): 2612–24. http://dx.doi.org/10.1135/cccc19932612.

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The excess volumes of twenty binary mixtures of four aromatic hydrocarbons (benzene, toluene, ethylbenzene, and p-xylene) and five linear alkanols (methanol, ethanol, 1-propanol, 1-butanol, and 1-pentanol) at 20 °C are reported. The excess volume of systems with the same alkanol increases with increasing size and number of substituents on the benzene ring. For systems with the same aromatic hydrocarbon it increases with the length of the alkanols. The dependence of ∆V/φ1ϑ2 values on composition is noticeably asymmetric. Systems with benzene as one of the component show larger ∆V/φ1ϑ2 values th
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Dissertations / Theses on the topic "Alkanol"

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Lam, Daniel H. "Multiphase equilibrium behavior of ethane, nitrous oxide and carbon dioxide + n-alkanol binary and ternary mixtures /." Access abstract and link to full text, 1990. http://0-wwwlib.umi.com.library.utulsa.edu/dissertations/fullcit/9034205.

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Amadio, Emanuele <1981&gt. "Oxidative carbonylation of alkanols catalyzed by Pd(II)-phosphine complexes." Doctoral thesis, Università Ca' Foscari Venezia, 2010. http://hdl.handle.net/10579/946.

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The complexes trans–[Pd(COOR)(H2O)(PPh3)2](TsO) (R = Me, Et, nPr, iPr, nBu, iBu, secBu) and trans–[Pd(COOR)nX2–n(PPh3)] (R = Me, n = 1, 2; X = ONO2, ONO, OTs, Br. R = iPr, n = 1, X = Cl, Br) have been synthesised and characterised. Most of them have been used as catalyst precursors for the oxidative carbonylation of MeOH, selective to dimethyloxalate, using p–benzoquinone (BQ) as an oxidant. BQ changes properties of the reaction centre. When using iPrOH in place of MeOH, high activity and selectivity toward diisopropyloxalate have been achieved using trans–[PdX2(PAr3)2] with strongly coordinat
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Wang, Zhong. "Synthesis of bioactive fluorinated bile acid analogues and investigating the influence of (deoxo)fluorination on alkanol and carbohydrate lipophilicity by a new logP determination method." Thesis, University of Southampton, 2016. https://eprints.soton.ac.uk/397966/.

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Since the identification of bile acids as natural ligands for FXR and TGR5 receptors, huge interest has arisen in this field, including the synthesis of semi-synthetic bile acid derivatives to increase binding potency and selectivity. Fluorine introduction is an attractive strategy in drug design and property optimization. This thesis describes the synthesis of fluorinated analogues of bile acids and the lead compound 6-ECDCA. Interesting observations of effects of fluorination on crystal packing modes will also be discussed. Another important application of fluorination is lipophilicity (logP
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Wassermann, Tobias N. "Umgebungseinflüsse auf die C-C- und C-O-Torsionsdynamik in Molekülen und Molekülaggregaten Schwingungsspektroskopie bei tiefen Temperaturen." Berlin Logos, 2009. http://d-nb.info/1000809706/04.

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Khalil, Enam A. S. A. "A thermodynamic study of binary and ternary mixtures of some alkanes and alkanols." Thesis, University of Manchester, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.328889.

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Favre, Éric. "Modélisation de l'équilibre de sorption et du transfert de matière dans des membranes à base de polydiméthylsiloxane : application à l'extraction d'alcanols de solutions aqueuses par pervaporation." Vandoeuvre-les-Nancy, INPL, 1994. http://docnum.univ-lorraine.fr/public/INPL_T_1994_FAVRE_E.pdf.

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Le but de ce travail est d'étudier l'extraction de composés organiques de solutions aqueuses par pervaporation sous l'angle du transfert de matière dans la membrane; l'équilibre de sorption et la diffusion de l'eau et d'une série d'alcanols (éthanol à pentanols) dans le polydimethylsiloxane (PDMS) ont été étudiés. La théorie de Flory-Huggins classique ne permet pas de décrire correctement les isothermes de sorption obtenus; une analyse des données d'équilibre, basée sur un critère thermodynamique (Zimm & Lundberg), montre que les molécules d'alcanols ont une tendance à l'autoassociation dans l
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ZHENG, TAO. "MOLECULAR SIMULATION OF DIFFUSION AND SORPTION OF ALKANES AND ALKANE MIXTURES IN POLY[1-(TRIMETHYLSILYL)-1-PROPYNE]." University of Cincinnati / OhioLINK, 2000. http://rave.ohiolink.edu/etdc/view?acc_num=ucin973701057.

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Correia, Leslie Daniel Camara. "Oxygen transfer in hydrocarbon-aqueous dispersions and its applicability to alkane-based bioprocesses." Thesis, Link to the online version, 2007. http://hdl.handle.net/10019/999.

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Criswell, Leah. "Neutron diffraction and quasielastic neutron scattering studies of films of N-alkanes and a branched alkane absorbed on graphite." Diss., Columbia, Mo. : University of Missouri-Columbia, 2007. http://hdl.handle.net/10355/6010.

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Thesis (Ph. D.)--University of Missouri-Columbia, 2007.<br>The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Title from title screen of research.pdf file (viewed on March 11, 2008) Includes bibliographical references.
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Cheema, Shabaz Ahmad. "The atmospheric oxidation of alkanols." Thesis, University of Hull, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.310212.

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Books on the topic "Alkanol"

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Tauginas, Darius. Alkanos sielos: Romanas. Alma littera, 2008.

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Yang, Li. Synthesis and characterisation of oligomer distributions of alkanol ethoxylates and characterisationof structural changes during oxidative thermal degradation of poly(alkylene glycols) by high resolution 1H and 13C NMR. University of Manchester, 1994.

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Hiemstra, H. Alkanes. Thieme, 2009.

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Marzullo, Benedetto. Alkaios' “Mirage”. Walter de Gruyter, 2008. http://dx.doi.org/10.1515/9783110210408.

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Kassühlke, R. Deftere Allah: Alkawal B̳ooymawal bee Alkawal Kesal. Alliance biblique du Cameroun, 1995.

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Szilárd, Borbély. Mint minden alkalom. József Attila Kör, 1995.

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Pombeiro, Armando J. L., and M. Fátima C. Guedes da Silva, eds. Alkane Functionalization. John Wiley & Sons, Ltd, 2019. http://dx.doi.org/10.1002/9781119379256.

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Patai, Saul, and Zvi Rappoport, eds. Alkanes and Cycloalkanes (1992). John Wiley & Sons, Ltd, 1992. http://dx.doi.org/10.1002/0470034378.

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International IUPAC Workshop on Vapor-Liquid Equilibria in 1-Alkanol [and] n-Alkane Mixtures (2nd 1985 Paris). Measurement, evaluation and prediction of phase equilibria: A collection of selected papers from the Second International IUPAC Workshop on Vapor-Liquid Equilibria in 1-Alkanol [and] n-Alkane Mixtures, Paris, France 5-7 September 1985 : and the Second International Symposium on Critical Evaluation and Prediction of Phase Equilibria in Multicomponent Systems, Paris, France 11-13 September 1985. Elsevier, 1986.

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V, Kehiaian H., Renon H, and International Symposium on Critical Evaluation and Prediction of Phase Equilibria in Multicomponent Systems (2nd : 1985 : Paris, France), eds. Measurement, evaluation, and prediction of phase equilibria: A collection of selected papers from the Second International IUPAC Workshop on Vapor-Liquid Equilibria in 1-Alkanol +n-Alkane Mixtures, Paris, France, 5-7 September 1985 and the Second International Symposium on Critical Evaluation and Prediction of Phase Equilibria in Multicomponent Systems, Paris France, 11-13 September 1985. Elsevier, 1986.

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Book chapters on the topic "Alkanol"

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Soai, Kenso, and Tsuneomi Kawasaki. "Asymmetric Autocatalysis of Pyrimidyl Alkanol." In Inventing Reactions. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/3418_2012_48.

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Jennings, David W., Michael T. Gude, and Amyn S. Teja. "High-Pressure Vapor—Liquid Equilibria in Carbon Dioxide and 1-Alkanol Mixtures." In ACS Symposium Series. American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0514.ch002.

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Schlossman, Mark L., and Aleksey M. Tikhonov. "X-ray Scattering Studies of Long-Chain Alkanol Monolayers at the Water-Hexane Interface." In ACS Symposium Series. American Chemical Society, 2003. http://dx.doi.org/10.1021/bk-2003-0861.ch006.

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Nakagawa, Tetsuo. "Microscale Experiment on Decreases in Volume When Forming Binary Liquid Mixtures: Four Alkanol Aqueous Solutions." In Chemistry Education and Sustainability in the Global Age. Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-4860-6_29.

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Latscha, Hans Peter, and Helmut Alfons Klein. "Alkohole (Alkanole)." In Springer-Lehrbuch. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-97539-4_35.

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Latscha, Hans Peter, Helmut Alfons Klein, and Rainer Mosebach. "Alkohole (Alkanole)." In Heidelberger Taschenbücher. Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-97065-8_13.

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Terang, Wearank, and Sabyasachi Banerjee. "An Insight into the Therapeutic Potential of Alkanet (Alkanna tinctoria)." In Medicinal Spices and Herbs from India. Apple Academic Press, 2024. http://dx.doi.org/10.1201/9781003511694-8.

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Nesselrath, Heinz-Günther. "Alkaios." In Kindlers Literatur Lexikon (KLL). J.B. Metzler, 2020. http://dx.doi.org/10.1007/978-3-476-05728-0_7605-1.

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Quintas, Louis V., and Edgar G. DuCasse. "Alkanes." In New Frontiers in Nanochemistry. Apple Academic Press, 2020. http://dx.doi.org/10.1201/9780429022937-2.

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Nünlist, René. "Alkaios." In Kleines Lexikon griechischer Autoren. J.B. Metzler, 2015. http://dx.doi.org/10.1007/978-3-476-05455-5_3.

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Conference papers on the topic "Alkanol"

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Hirano, Susumu, and Tatsuya Sei. "Influence of Hydrocarbon on Stearic Acid as Corrosion Inhibitor in Synthetic Brine." In CONFERENCE 2023. AMPP, 2023. https://doi.org/10.5006/c2023-19330.

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Abstract The role of corrosion inhibitor is explained by the function of surfactant, i.e., partition from oil to water, dispersion in water and adsorption on metal surface. This study selected stearic acid as a surfactant and paid attention to the effect of oil on corrosion inhibition. Stearic acid was treated as a single component corrosion inhibitor. The corrosion inhibitor efficiency of stearic acid was observed in a metal-oil-water system. An acyclic saturated hydrocarbon, i.e., an alkane was tested as oil because it has a simple chemical structure. Stearic acid was dissolved in alkanes an
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Tanji, Yasunori, Kazuya Toyama, and Kazuhiko Miyanaga. "Identification of Crude Oil Component Which Facilitate Biological Souring." In CORROSION 2014. NACE International, 2014. https://doi.org/10.5006/c2014-3853.

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Abstract Seawater injection into oil reservoirs for secondary oil recovery is frequently accompanied by souring (increased sulfide concentrations). Production of hydrogen sulfide causes various problems, such as microbiologically influenced corrosion (MIC), deterioration of crude oil. Sulfate-reducing bacteria (SRB) are considered to be major players in souring. Volatile fatty acids (VFAs) in oil field water are assumed to be produced by microbial degradation of crude oil. The objective of this research is to investigate mechanisms of souring from the view of VFA production by the crude oil bi
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Sy, Mohamed, Ali Elkhazraji, Mohammed S. Khan, Pan Luo, Ibrahim Atwah, and Aamir Farooq. "ML-Enhanced Laser-Based Analyzer for Selective C1-C5 Alkanes Detection." In Laser Applications to Chemical, Security and Environmental Analysis. Optica Publishing Group, 2024. https://doi.org/10.1364/lacsea.2024.lm1f.5.

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A laser sensor is developed for selective and simultaneous measurement of C1-C5 alkanes in natural gas samples. Utilizing a DFB-ICL near 3.3 µm and employing CNNs, it distinguishes overlapping absorbance spectra of C1-C5 alkanes and isomer species.
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Hirano, Susumu, Tatsuya Sei, Midori Kawasaki, and Atsushi Kobayashi. "Understanding of Corrosion Inhibitor Behavior through Interaction between Stearic Acid and Alkane." In CONFERENCE 2024. AMPP, 2024. https://doi.org/10.5006/c2024-20900.

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Abstract A principle of corrosion inhibitor behavior in an oil pipeline was studied with stearic acid and alkane. The role of corrosion inhibitor is explained by the function of surfactant, i.e., partition from oil to water, dispersion in water and adsorption on metal surface. Stearic acid alkane solution was treated as a single component model inhibitor. The performance of the model inhibitor was evaluated by measuring corrosion rates of carbon steel in a metal-oil-water system. Interfacial tension and total organic carbon were measured to investigate the dispersion of the model inhibitor. Th
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Dowling, N. J. E., J. Bullen, D. C. White, and W. R. Finnerty. "Biocorrosion of Carbon Steel by an Alkane–Utilizing Microorganism." In CORROSION 1991. NACE International, 1991. https://doi.org/10.5006/c1991-91276.

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Abstract Carbon steel exhibited accelerated rates of corrosion when placed in contact with a mineral salts medium supporting the growth of Rhodococcus species H-13A with hexadecane as the sole source of carbon and energy. Contact of the carbon steel with identical sterile medium resulted in pristine surfaces on the coupons after 4 days of exposure; whereas, the presence of exponential growth phase cultures created a blackened, undulant and highly corroded surface. Exponential growth phase cultures are characterized by high oxygen demand, the production of extracellular biosurfactant and the fo
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KANG, JEONG WON, CHUNG HOON KWON, CHUL SOO LEE, and KI-PUNG YOO. "EXCESS MOLAR ENTHALPIES FOR BINARY SYSTEMS OF N-ALKANE +1-ALKANOL SYSTEMS AT 313.15 K." In Proceedings of the 4th International Conference. WORLD SCIENTIFIC, 2004. http://dx.doi.org/10.1142/9789812702623_0009.

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Soai, Kenso, Tsuneomi Kawasaki, Enrique Díaz-Herrera, and Eusebio Juaristi. "Symmetry Breaking in Asymmetric Autocatalysis of Pyrimidyl Alkanol." In 2007. AIP, 2008. http://dx.doi.org/10.1063/1.2901849.

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Kawaguchi, Touru, Gota Kikugawa, Ikuya Kinefuchi, Taku Ohara, Shinichi Yatuzuka, and Yoichiro Matsumoto. "Molecular Dynamics Study of Interfacial Thermal Resistance of Mercapto-Alkanol Self-Assembled Monolayer and Water." In ASME 2009 Second International Conference on Micro/Nanoscale Heat and Mass Transfer. ASMEDC, 2009. http://dx.doi.org/10.1115/mnhmt2009-18424.

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The interfacial thermal resistance of 11-mercaptoundecanol (-S(CH2)11OH) self-assembled monolayer (SAM) adsorbed on Au(111) substrate and water was investigated using nonequilibrium molecular dynamics simulations. The interfacial thermal resistance was found to be a half of that in the system which consists of 1-dodecanthiol (-S(CH2)11CH3) SAM adsorbed on Au(111) and toluene [Kikugawa G. et al., J. Chem. Phys. (2009)]. The effective thermal energy transfer originates from hydrogen-bond structure between the SAM and water molecules in spite of weak structurization of water molecules near the SA
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Yin, Sudong, Yanglin Pan, and Zhongchao Tan. "Catalytic Hydrothermal Conversion of Glucose to Light Petroleum Alkanes." In ASME 2010 4th International Conference on Energy Sustainability. ASMEDC, 2010. http://dx.doi.org/10.1115/es2010-90433.

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The production of carbon-neutral liquid fuels from renewable biomass has attracted worldwide interest in an age of depletion of fossil fuel reserves and pollutions caused by utilization of fossil petroleum. Currently, commercial bio-oil production technologies include bio-ethanol, bio-diesel and pyrolysis bio-oil. But, these bio-oils mainly consist of alcohols and aromatic chemicals rather than alkanes of the main components of gasoline and diesel. Direct utilization of these bio-oils can corrode car engines as well as emitting large unburned hydrocarbons particles through automotive combustio
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Leyva Gutierrez, Francisco, and Tong Wang. "Crystallography and Functionality of Natural Waxes: Insights for the Development of Tailored Lipid Materials." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/nyok4571.

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Natural waxes are valuable industrial products consisting of complex chemical mixtures. To probe the structure−function role of select constituents, model n-alkanes, alcohols, aldehydes, and fatty acids of C18−19, C22−23, and C26−27 carbon chain lengths were synthesized and analyzed via calorimetry and X-ray powder diffraction. Pure compounds and binary mixtures crystallized into monoclinic (M), triclinic (T), and orthorhombic (O) lattices or combinations thereof. The C26 aldehyde formed an O lattice and exhibited one solid−solid phase transition similar to n-alkanes. The water vapor permeabil
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Reports on the topic "Alkanol"

1

Scott Han. Millisecond Oxidation of Alkanes. Office of Scientific and Technical Information (OSTI), 2011. http://dx.doi.org/10.2172/1025808.

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Lyons, J. E. Catalytic conversion of light alkanes. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/7090637.

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Crabtree, R. H. (Alkane photoreactions with mercury vapor). Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6454222.

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4

Cesar, J. R., and O. H. Ardakani. Organic geochemistry of the Montney Formation: new insights about the source of hydrocarbons, their accumulation history and post accumulation processes. Natural Resources Canada/CMSS/Information Management, 2022. http://dx.doi.org/10.4095/329788.

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This study consists of a non-traditional molecular and stable isotope approach to analyze organic matter (soluble bitumen and produced oil/condensate) from the Montney Formation low-permeability reservoirs, with the purpose of identifying source(s) of hydrocarbons, accumulation history and post accumulation processes. The same approach bases on the distribution of compound classes such as aromatic carotenoids, polycyclic aromatic hydrocarbons (PAHs), bicyclic alkanes, and oxygen-polar compounds. The geochemical screening has been enhanced with performing compound specific isotope analysis (CSI
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5

Doskey, P. V. The vapor-particle partitioning of n-alkanes. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10141716.

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Deutsch, M., B. M. Ocko, X. Z. Wu, E. B. Sirota, and S. K. Sinha. Surface crystallization in normal-alkanes and alcohols. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/80963.

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Stambuli, James P., and S. M. Whittemore. Site-selective Alkane Dehydrogenation of Fatty Acids. Defense Technical Information Center, 2011. http://dx.doi.org/10.21236/ada566294.

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Wu, X. Z., H. H. Shao, B. M. Ocko, et al. Surface crystallization and thin film melting in normal alkanes. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10117552.

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9

Lyons, J. E. Catalytic conversion of light alkanes: Proof of concept stage. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/67783.

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10

Lyons, J. E. Catalytic conversion of light alkanes. [Methane, ethane, propane and butanes]. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/7090643.

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