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Journal articles on the topic 'Decanol'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

To Quynh, Cung Thi. "STUDY ON THE AROMA MODEL OF VIETNAMESE CORIANDER LEAVES (Polygonum odoratum)." Vietnam Journal of Science and Technology 54, no. 4A (2018): 73. http://dx.doi.org/10.15625/2525-2518/54/4a/11980.

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The volatiles present in fresh Vietnamese coriander (Polygonum odoratum) were isolated by solvent extraction and analyzed by GC analyses, aroma extract dilution analysis and omission test. The fresh herb was characterized as green, citrusy, pungent, and floral odors. The saturated aldehydes C10,C11, C12, hexanal and decanol were most likely the principal contributors to Vietnamese coriander's characteristic aroma. The aroma reconstitution was finally examined by sensory evaluation methods based on the 5 key odorants mentioned above. The results of the omission experiments confirmed that dodeca

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2

RILEY, M. "Decomposition of decanol and decanal over Ni- and H-ZSM-5." Journal of Catalysis 103, no. 1 (1987): 87–94. http://dx.doi.org/10.1016/0021-9517(87)90095-9.

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3

Rong, Guo, Zhu Xia-Shi, and Yan Peng-Quan. "The Liquid Crystal Structure Between System SDS/Decanol/Glycerol and SDS/Decanol/Formamide." Acta Physico-Chimica Sinica 8, no. 05 (1992): 664–67. http://dx.doi.org/10.3866/pku.whxb19920517.

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4

Kwon, Kyungok, Dongwon Lee, Yusaku Iwata, and Hiroshi Koseki. "Flash points of n-decanol." Journal of Loss Prevention in the Process Industries 21, no. 4 (2008): 478–80. http://dx.doi.org/10.1016/j.jlp.2007.11.002.

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5

Ali, Abbas, Nurhayat Tabanca, Betul Demirci, et al. "Insecticidal and Biting Deterrent Activities of Magnolia grandiflora Essential Oils and Selected Pure Compounds against Aedes aegypti." Molecules 25, no. 6 (2020): 1359. http://dx.doi.org/10.3390/molecules25061359.

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In our natural products screening program for mosquitoes, we tested essential oils extracted from different plant parts of Magnolia grandiflora L. for their insecticidal and biting deterrent activities against Aedes aegypti. Biting deterrence of seeds essential oil with biting deterrence index value of 0.89 was similar to N,N-diethyl-3-methylbenzamide (DEET). All the other oils were active above the solvent control but the activity was significantly lower than DEET. Based on GC-MS analysis, three pure compounds that were only present in the essential oil of seed were further investigated to id

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6

Sun, Daolai, Takuya Misu, Yasuhiro Yamada, and Satoshi Sato. "Advantages of using Cu/SiO2 catalyst for vapor-phase dehydrogenation of 1-decanol into decanal." Applied Catalysis A: General 582 (July 2019): 117109. http://dx.doi.org/10.1016/j.apcata.2019.06.007.

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7

Neumann, Grit, Nadja Kabelitz, Andreas Zehnsdorf, et al. "Prediction of the Adaptability of Pseudomonas putida DOT-T1E to a Second Phase of a Solvent for Economically Sound Two-Phase Biotransformations." Applied and Environmental Microbiology 71, no. 11 (2005): 6606–12. http://dx.doi.org/10.1128/aem.71.11.6606-6612.2005.

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ABSTRACT The strain Pseudomonas putida DOT-T1E was tested for its ability to tolerate second phases of different alkanols for their use as solvents in two-liquid-phase biotransformations. Although 1-decanol showed an about 10-fold higher toxicity to the cells than 1-octanol, the cells were able to adapt completely to 1-decanol only and could not be adapted in order to grow stably in the presence of a second phase of 1-octanol. The main explanation for this observation can be seen in the higher water and membrane solubility of 1-octanol. The hydrophobicity (log P) of a substance correlates with

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8

Čejková, Jitka, František Štěpánek, and Martin M. Hanczyc. "Evaporation-Induced Pattern Formation of Decanol Droplets." Langmuir 32, no. 19 (2016): 4800–4805. http://dx.doi.org/10.1021/acs.langmuir.6b01062.

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9

Mao, X. H. "Stripping of titanium from TBP-decanol phase." IOP Conference Series: Materials Science and Engineering 164 (January 2017): 012029. http://dx.doi.org/10.1088/1757-899x/164/1/012029.

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10

Friberg, Stig E., Steven M. Jones, and C. C. Yang. "GELATION OF FORMAMIDE - CETYLTRIMETHYLAMMONIUM BROMIDE -DECANOL MICROEMOLSIONS." Journal of Dispersion Science and Technology 13, no. 1 (1992): 45–63. http://dx.doi.org/10.1080/01932699208943295.

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11

Hendrikx, Y., and J. Charvolin. "Deformation of cylinders in the hexagonal phase of sodium decyl sulphate/decanol/water on the introduction of decanol." Liquid Crystals 3, no. 2 (1988): 265–73. http://dx.doi.org/10.1080/02678298808086373.

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12

Čejková, Jitka, Martin M. Hanczyc, and František Štěpánek. "Multi-Armed Droplets as Shape-Changing Protocells." Artificial Life 24, no. 1 (2018): 71–79. http://dx.doi.org/10.1162/artl_a_00255.

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Protocells are objects that mimic one or several functions of biological cells and may be embodied as solid particles, lipid vesicles, or droplets. Our work is based on using decanol droplets in an aqueous solution of sodium decanoate in the presence of salt. A decanol droplet under such conditions bears many qualitative similarities with living cells, such as the ability to move chemotactically, divide and fuse, or change its shape. This article focuses on the description of a shape-changing process induced by the evaporation of water from the decanoate solution. Under these conditions, the d

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13

Neumann, Grit, Sjef Cornelissen, Frank van Breukelen, et al. "Energetics and Surface Properties of Pseudomonas putida DOT-T1E in a Two-Phase Fermentation System with 1-Decanol as Second Phase." Applied and Environmental Microbiology 72, no. 6 (2006): 4232–38. http://dx.doi.org/10.1128/aem.02904-05.

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ABSTRACT The solvent-tolerant strain Pseudomonas putida DOT-T1E was grown in batch fermentations in a 5-liter bioreactor in the presence and absence of 10% (vol/vol) of the organic solvent 1-decanol. The growth behavior and cellular energetics, such as the cellular ATP content and the energy charge, as well as the cell surface hydrophobicity and charge, were measured in cells growing in the presence and absence of 1-decanol. Although the cells growing in the presence of 1-decanol showed an about 10% reduced growth rate and a 48% reduced growth yield, no significant differences were measured ei

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14

Spaccini, Raffaele, Anna Tsoukala, Lucia Liguori, Carlo Punta, and Hans-René Bjørsvik. "An Optimized Process to 10-Bromo-1-decanol." Organic Process Research & Development 14, no. 5 (2010): 1215–20. http://dx.doi.org/10.1021/op100143t.

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15

Teixeira, Cilâine Verônica, Rosangela Itri, and Lia Queiroz do Amaral. "Decanol Effect on Micellar Structure and Phase Transitions." Langmuir 15, no. 4 (1999): 936–39. http://dx.doi.org/10.1021/la980606p.

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16

Lehmler, Hans-Joachim, and Paul M. Bummer. "Mixing behavior of 10-(perfluorohexyl)-decanol and DPPC." Colloids and Surfaces B: Biointerfaces 44, no. 2-3 (2005): 74–81. http://dx.doi.org/10.1016/j.colsurfb.2005.05.014.

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17

Suryabrahmam, Buti, Ayush Agrawal, and V. A. Raghunathan. "Fluid–fluid coexistence in phospholipid membranes induced by decanol." Soft Matter 16, no. 39 (2020): 9002–5. http://dx.doi.org/10.1039/d0sm01417f.

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18

Ruiz-Fernández, A. R., J. J. López-Cascales, J. J. Giner-Casares, R. Araya-Maturana, F. G. Díaz-Baños, and B. E. Weiss-López. "Composition effect on the aggregate/solution interface of a nematic lyotropic liquid crystal." RSC Advances 6, no. 88 (2016): 85411–19. http://dx.doi.org/10.1039/c6ra13597h.

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19

M., Ramya, Nideep T. K., Nampoori V. P. N., and Kailasnath M. "Understanding the role of alcohols in the growth behaviour of ZnO nanostructures prepared by solution based synthesis and their application in solar cells." New Journal of Chemistry 43, no. 46 (2019): 17980–90. http://dx.doi.org/10.1039/c9nj03212f.

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20

Rutter, Charles D., and Christopher V. Rao. "Production of 1-decanol by metabolically engineered Yarrowia lipolytica." Metabolic Engineering 38 (November 2016): 139–47. http://dx.doi.org/10.1016/j.ymben.2016.07.011.

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21

Friberg, Stig E., Teanoosh Moaddel, and Estel D. Sprague. "Association Structures in Water, Poly(sodium undecanoate), and Decanol." Journal of Physical Chemistry 98, no. 50 (1994): 13414–17. http://dx.doi.org/10.1021/j100101a048.

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22

Arabia, G., G. Chidichimo, A. Golemme, and P. Ukleja. "Water ordering in a MTAB/decanol/water lyotropic system." Liquid Crystals 10, no. 3 (1991): 311–23. http://dx.doi.org/10.1080/02678299108026278.

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23

Hiasa, Takumi, Kenjiro Kimura, and Hiroshi Onishi. "Cross-Sectional Structure of Liquid 1-Decanol over Graphite." Journal of Physical Chemistry C 116, no. 50 (2012): 26475–79. http://dx.doi.org/10.1021/jp310203s.

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24

Patton, Christi L., and Kraemer D. Luks. "Multiphase equilibria of the binary mixture xenon + 1-decanol." Fluid Phase Equilibria 98 (July 1994): 201–11. http://dx.doi.org/10.1016/0378-3812(94)80119-3.

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25

Lin, Shi-Yow, Ting-Li Lu, and Woei-Bor Hwang. "Adsorption Kinetics of Decanol at the Air-Water Interface." Langmuir 11, no. 2 (1995): 555–62. http://dx.doi.org/10.1021/la00002a033.

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26

Sampaio, Anderson Reginaldo, Newller Marcelo Kimura, Bruna Luíza Pelegrini, Marli Miriam de Souza Lima, and Marcus Bastos Lacerda Santos. "Decanol effect on viscoelasticity and rheology in lamellar mesophases." Phase Transitions 90, no. 8 (2017): 790–99. http://dx.doi.org/10.1080/01411594.2017.1290803.

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27

Zhu, Wenjie, Xuemin He, Shaohua Huang, and Jing Yan. "Bioluminescence of vibrio orientals in vitro: Decanol initiated bioluminescence." Journal of Luminescence 40-41 (February 1988): 225–26. http://dx.doi.org/10.1016/0022-2313(88)90166-4.

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28

McGachy, Lenka, Jan Heyda, Jan Tomas, and Jitka Čejková. "Decanol pattern formation over a sessile aqueous decanoate droplet." Colloids and Surfaces A: Physicochemical and Engineering Aspects 621 (July 2021): 126541. http://dx.doi.org/10.1016/j.colsurfa.2021.126541.

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29

Zhang, Ming, Yajie Zhao, Qian Liu, Lan Yang, Guoli Fan, and Feng Li. "A La-doped Mg–Al mixed metal oxide supported copper catalyst with enhanced catalytic performance in transfer dehydrogenation of 1-decanol." Dalton Transactions 45, no. 3 (2016): 1093–102. http://dx.doi.org/10.1039/c5dt03217b.

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A La-doped Mg–Al mixed metal oxide supported copper catalyst exhibited excellent catalytic performance in transfer dehydrogenation of 1-decanol due to the surface cooperation between Lewis basic sites and copper species.

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30

Deng, Chen-Qiang, Qin-Zhu Jiang, Jin Deng, and Yao Fu. "Synthesis of 1,10-decanediol diacetate and 1-decanol acetate from furfural." Green Chemistry 23, no. 5 (2021): 2169–76. http://dx.doi.org/10.1039/d1gc00227a.

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Furfural was converted into furoin by immobilized NHC catalyst, and then furoin was upgraded into 1,10-decanediol diacetate and 1-decanol acetate by Pd/C catalytic hydrodeoxygenation reaction promoted with Sc(OTf)<sub>3 </sub>in acetic acid.

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31

Karabagias, Karabagias, and Badeka. "The Honey Volatile Code: A Collective Study and Extended Version." Foods 8, no. 10 (2019): 508. http://dx.doi.org/10.3390/foods8100508.

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Background: The present study comprises the second part of a new theory related to honey authentication based on the implementation of the honey code and the use of chemometrics. Methods: One hundred and fifty-one honey samples of seven different botanical origins (chestnut, citrus, clover, eucalyptus, fir, pine, and thyme) and from five different countries (Egypt, Greece, Morocco, Portugal, and Spain) were subjected to analysis of mass spectrometry (GC-MS) in combination with headspace solid-phase microextraction (HS-SPME). Results: Results showed that 94 volatile compounds were identified an

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32

Covarelli, L. "Studies on the control of broomrape (Orobancheramosa L.) in Virginia tobacco (Nicotianatabacum L.)." Beiträge zur Tabakforschung International/Contributions to Tobacco Research 20, no. 2 (2002): 77–81. http://dx.doi.org/10.2478/cttr-2013-0733.

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AbstractDuring 1997 and 1998, in the province of Perugia (Umbria, central Italy), four field experimental trials were carried out to study the control of broomrape (OrobancheramosaL.) in Virginia tobacco. In 1997, maleic hydrazide (2040 mL ha-1), flumetralin (1200 mL ha-1), n-decanol (10720 mL ha-1), glyphosate (180-324 mL ha-1) and rimsulfuron (12.5-25 g ha-1) were tested on the variety K 394. In the second year, maleic hydrazide (2040 mL ha-1), n-decanol (10720 mL ha-1) and butralin (2160 mL ha-1) were utilised in the same variety. Furthermore, a field experiment was performed to assess the

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33

Amaral, L. Q., and M. E. Marcondes Helene. "Nematic domain in the sodium lauryl sulfate/water/decanol system." Journal of Physical Chemistry 92, no. 21 (1988): 6094–98. http://dx.doi.org/10.1021/j100332a049.

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34

Lam, Daniel H., and Kraemer D. Luks. "Multiphase equilibrium behavior of the mixture ethane + methanol + 1-decanol." Journal of Chemical & Engineering Data 36, no. 3 (1991): 307–11. http://dx.doi.org/10.1021/je00003a014.

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35

Choi, Sooseok, and Takayuki Watanabe. "Decomposition of 1-Decanol Emulsion by Water Thermal Plasma Jet." IEEE Transactions on Plasma Science 40, no. 11 (2012): 2831–36. http://dx.doi.org/10.1109/tps.2012.2206059.

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36

Berger, K., and K. Hiltrop. "Characterization of structural transitions in the SLS/decanol/water system." Colloid & Polymer Science 274, no. 3 (1996): 269–78. http://dx.doi.org/10.1007/bf00665644.

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37

El-Seesy, Ahmed I., Radwan M. El-Zoheiry, Abdelrahman K. Fouad, et al. "Impacts of octanol and decanol addition on the solubility of methanol/hydrous methanol/diesel/biodiesel/Jet A-1 fuel ternary mixtures." RSC Advances 11, no. 30 (2021): 18213–24. http://dx.doi.org/10.1039/d1ra01625c.

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This study attempts to enhance the mixture instability of methanol/hydrous methanol mixed with diesel fuel, waste cooking oil biodiesel, and Jet A-1 fuel using n-octanol and n-decanol as cosolvent at numerous temperatures of 10 °C, 20 °C, and 30 °C.

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38

Wahlen, Bradley D., Whitney S. Oswald, Lance C. Seefeldt, and Brett M. Barney. "Purification, Characterization, and Potential Bacterial Wax Production Role of an NADPH-Dependent Fatty Aldehyde Reductase from Marinobacter aquaeolei VT8." Applied and Environmental Microbiology 75, no. 9 (2009): 2758–64. http://dx.doi.org/10.1128/aem.02578-08.

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ABSTRACT Wax esters, ester-linked fatty acids and long-chain alcohols, are important energy storage compounds in select bacteria. The synthesis of wax esters from fatty acids is proposed to require the action of a four-enzyme pathway. An essential step in the pathway is the reduction of a fatty aldehyde to the corresponding fatty alcohol, although the enzyme responsible for catalyzing this reaction has yet to be identified in bacteria. We report here the purification and characterization of an enzyme from the wax ester-accumulating bacterium Marinobacter aquaeolei VT8, which is a proposed fatt

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39

Rojas, Antonia, Estrella Duque, Andreas Schmid, Ana Hurtado, Juan-Luis Ramos, and Ana Segura. "Biotransformation in Double-Phase Systems: Physiological Responses of Pseudomonas putida DOT-T1E to a Double Phase Made of Aliphatic Alcohols and Biosynthesis of Substituted Catechols." Applied and Environmental Microbiology 70, no. 6 (2004): 3637–43. http://dx.doi.org/10.1128/aem.70.6.3637-3643.2004.

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ABSTRACT Pseudomonas putida strain DOT-T1E is highly tolerant to organic solvents, with a logPow (the logarithm of the partition coefficient of a solvent in a two-phase water-octanol system of ≥2.5. Solvent tolerant microorganisms can be exploited to develop double-phase (organic solvent and water) biotransformation systems in which toxic substrates or products are kept in the organic phase. We tested P. putida DOT-T1E tolerance to different aliphatic alcohols with a logPow value between 2 and 4, such as decanol, nonanol, and octanol, which are potentially useful in biotransformations in doubl

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40

Kirbaslar, S. I. "Liquid - liquid equilibria of the water + butyric acid + decanol ternary system." Brazilian Journal of Chemical Engineering 23, no. 3 (2006): 365–74. http://dx.doi.org/10.1590/s0104-66322006000300010.

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41

Zhang, B., G. Gozzelino, and G. Baldi. "Membrane liquid loss of supported liquid membrane based on n-decanol." Colloids and Surfaces A: Physicochemical and Engineering Aspects 193, no. 1-3 (2001): 61–70. http://dx.doi.org/10.1016/s0927-7757(01)00688-4.

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42

Shin, Jungin, Moon Sam Shin, Won Bae, Youn-Woo Lee, and Hwayong Kim. "High-pressure phase behavior of carbon dioxide+heptadecafluoro-1-decanol system." Journal of Supercritical Fluids 44, no. 3 (2008): 260–65. http://dx.doi.org/10.1016/j.supflu.2007.09.023.

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43

Friberg, S. E., Guo Rong, and A. J. I. Ward. "Phase diagram of the system formamide-sodium dodecyl sulfate-decanol-toluene." Journal of Physical Chemistry 92, no. 26 (1988): 7247–51. http://dx.doi.org/10.1021/j100337a017.

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44

Charvolin, Jean. "Evolution of cylindrical structures in the system sodium decylsulphate/decanol/water." Liquid Crystals 13, no. 6 (1993): 829–42. http://dx.doi.org/10.1080/02678299308027296.

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45

Plumley, S., Y. K. Zhu, Y. W. Hui, and A. Saupe. "Rotational Viscosities of Nematic Sodium Decylsulfate, 1-Decanol, D2 O Mixtures." Molecular Crystals and Liquid Crystals 182, no. 1 (1990): 215–24. http://dx.doi.org/10.1080/00268949008035753.

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46

Patton, Christi L., and K. D. Luks. "Multiphase equilibrium behavior of the mixture ethane + 1-decanol + n-docosane." Fluid Phase Equilibria 85 (May 1993): 181–90. http://dx.doi.org/10.1016/0378-3812(93)80013-d.

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47

Stul’, B. Ya. "Kinetics of the n-Decanol Oxyethylation Reaction with Allowance for Association." Russian Journal of Physical Chemistry A 90, no. 4 (2016): 754–60. http://dx.doi.org/10.1134/s0036024416040282.

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48

Weiss, A., P. Schick, and D. Platikanov. "Bilayer studies in mixedn-decanol/n-tetradecanol complexes ofn-decylammonium beidellite." Colloid & Polymer Science 273, no. 6 (1995): 572–78. http://dx.doi.org/10.1007/bf00658687.

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49

Selivanova, Natalia M., Aidar T. Gubaidullin, Ksenia A. Romanova, and Yuriy G. Galyametdinov. "Modification of Nonionic Vesicles by Adding Decanol and Functional Lanthanide Ions." Journal of Surfactants and Detergents 20, no. 2 (2016): 309–19. http://dx.doi.org/10.1007/s11743-016-1911-y.

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50

Hendrikx, Y., J. Charvolin, P. Kekicheff, and M. Roth. "Structural fluctuations in the lamellar phase of sodium decyl sulphate/decanol/water." Liquid Crystals 2, no. 5 (1987): 677–87. http://dx.doi.org/10.1080/02678298708086326.

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