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Journal articles on the topic 'Ethanolamines'

Author: Grafiati

Published: 4 June 2021

Last updated: 18 February 2022

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1

Cheng, Hua Nong, Qing Shan Liu, Bing Qiang Wang, and Shi Qing Zheng. "Reaction Kinetics of Ethanolamines with Water Catalysis." Advanced Materials Research 233-235 (May 2011): 95–100. http://dx.doi.org/10.4028/www.scientific.net/amr.233-235.95.

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An experiment of the preparation of mono-ethanolamine, die-ethanolamine, and tri-ethanolamine from aqueous ammonia and ethylene oxide is studied. In the reaction system, water carries out the catalysis. The activation energy of mono-ethanolamine is determined, 61.52kJ.mol-1. The frequency factor is a quadratic function of water concentration. Under different reaction temperature, three final ethanolamine product contents are constant, which indicate the activation energies of three ethanolamins are equal. Using nonlinear least square regression, reaction rate ratios of die-ethanolamine or tri-ethanolamine to mono-ethanolamine are calculated. The two ratios are both linear relation with water concentration, dropping with water concentration increase.

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2

Filburn, T., J. J. Helble, and R. A. Weiss. "Development of Supported Ethanolamines and Modified Ethanolamines for CO2Capture." Industrial & Engineering Chemistry Research 44, no. 5 (March 2005): 1542–46. http://dx.doi.org/10.1021/ie0495527.

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3

Labban, Abdulkarim S., and Yizhak Marcus. "Solvatochromic parameters of ethanolamines." Journal of the Chemical Society, Faraday Transactions 93, no. 1 (1997): 77–79. http://dx.doi.org/10.1039/a605521d.

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4

Bakalova, S., V. Mincheva, A. Doycheva, V. Groudeva, and R. Dimkov. "Microbial Toxicity of Ethanolamines." Biotechnology & Biotechnological Equipment 22, no. 2 (January 2008): 716–20. http://dx.doi.org/10.1080/13102818.2008.10817540.

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5

Park, Donguk, Shinbum Kim, and Kwonchul Ha. "Relationships among Fluid Ethanolamine Formulation, Airborne Ethanolamines, and Aerosol Levels in Machining Operations." Aerosol and Air Quality Research 12, no. 4 (2012): 553–60. http://dx.doi.org/10.4209/aaqr.2012.01.0002.

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6

Brussee, J., F. Dofferhoff, C. G. Kruse, and A. Van Der Gen. "Synthesis of optically active ethanolamines." Tetrahedron 46, no. 5 (January 1990): 1653–58. http://dx.doi.org/10.1016/s0040-4020(01)81972-4.

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7

Savonius, B., H. Keskinen, M. Tuppurainen, and L. Kanerva. "Occupational asthma caused by ethanolamines." Allergy 49, no. 10 (December 1994): 877–81. http://dx.doi.org/10.1111/j.1398-9995.1994.tb00791.x.

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8

Wichmann, M., and M. Stockhausen. "Dielectric Relaxation of Three Ethanolamines." Zeitschrift für Naturforschung A 56, no. 8 (August 1, 2001): 603–4. http://dx.doi.org/10.1515/zna-2001-0811.

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Abstract Relaxation spectra have been measured at 20°C for mono-, di-and triethanolamine in the pure liquid state and in a 0.6 mole fraction mixture with 1,4-dioxane. The general resemblance to the dielectric behaviour of alcohols and aminoalcohols shows that relaxation is governed by association effects. In this regard, several features point to significantly differing behaviour of the mono compound in comparison with both di-and triethanol amine.

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9

DiGuilio, Ralph M., William L. McGregor, and Amyn S. Teja. "Thermal conductivities of the ethanolamines." Journal of Chemical & Engineering Data 37, no. 2 (April 1992): 242–45. http://dx.doi.org/10.1021/je00006a029.

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10

T. Vashi, R., H. M. Bhajiwala, and S. A. Desai. "Ethanolamines as Corrosion Inhibitors for Zinc in (HNO3+H2SO4) Binary Acid Mixture." E-Journal of Chemistry 7, no. 2 (2010): 665–68. http://dx.doi.org/10.1155/2010/518543.

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This work deals with the study of corrosion behaviour for zinc in (HNO3+ H2SO4) binary acid mixture containing ethanolamines. Corrosion rate increases with concentration of acid and temperature. At constant acid concentration, the inhibition efficiency of ethanolamines increases with the inhibitor concentration. Value of ΔGa increases and inhibition decreases with temperature. The mode of inhibition action appears to be chemisorption.

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11

Tsuhako, Mitsutomo, Chiyoko Sueyoshi, Tohru Miyajima, Shigeru Ohashi, Hiroyuki Nariai, and Itaru Motooka. "The Reaction ofcyclo-Triphosphate with Ethanolamines." Bulletin of the Chemical Society of Japan 59, no. 10 (October 1986): 3091–95. http://dx.doi.org/10.1246/bcsj.59.3091.

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12

DiGuilio, Ralph M., Rong Jwyn Lee, Steven T. Schaeffer, Laura L. Brasher, and Amyn S. Teja. "Densities and viscosities of the ethanolamines." Journal of Chemical & Engineering Data 37, no. 2 (April 1992): 239–42. http://dx.doi.org/10.1021/je00006a028.

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13

Melnyk, Stepan, Roman Danyliuk, Yuriy Melnyk, and Victor Reutskyy. "The Reaction of Oleic Acid with a Mixture of Ethanolamines." Chemistry & Chemical Technology 12, no. 1 (March 21, 2018): 13–17. http://dx.doi.org/10.23939/chcht12.01.013.

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14

Hansen, Harald S., Birthe Moesgaard, Gitte Petersen, and Henrik H. Hansen. "Putative neuroprotective actions of N-acyl-ethanolamines." Pharmacology & Therapeutics 95, no. 2 (August 2002): 119–26. http://dx.doi.org/10.1016/s0163-7258(02)00251-6.

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15

Zardini, Hadi Zare, Morteza Davarpanah, Mehdi Shanbedi, Ahmad Amiri, Morteza Maghrebi, and Leila Ebrahimi. "Microbial toxicity of ethanolamines-Multiwalled carbon nanotubes." Journal of Biomedical Materials Research Part A 102, no. 6 (June 28, 2013): 1774–81. http://dx.doi.org/10.1002/jbm.a.34846.

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16

Cheng, Xiaohong, Xiangjun Liu, Tao Bing, Rui Zhao, Shaoxiang Xiong, and Dihua Shangguan. "Specific DNA G-quadruplexes bind to ethanolamines." Biopolymers 91, no. 10 (October 2009): 874–83. http://dx.doi.org/10.1002/bip.21272.

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17

Billany, M. R., Kurshid Khatib, Marsha Gordon, and J. K. Sugden. "Alcohols and ethanolamines as hydroxyl radical scavengers." International Journal of Pharmaceutics 137, no. 2 (June 1996): 143–47. http://dx.doi.org/10.1016/0378-5173(96)04246-9.

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18

Manca, Claudia, Sébastien Lacroix, Francine Pérusse, Nicolas Flamand, Yvon Chagnon, Vicky Drapeau, Angelo Tremblay, Vincenzo Di Marzo, and Cristoforo Silvestri. "Oral Capsaicinoid Administration Alters the Plasma Endocannabinoidome and Fecal Microbiota of Reproductive-Aged Women Living with Overweight and Obesity." Biomedicines 9, no. 9 (September 17, 2021): 1246. http://dx.doi.org/10.3390/biomedicines9091246.

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Capsaicinoids, the pungent principles of chili peppers and prototypical activators of the transient receptor potential of the vanilloid type-1 (TRPV1) channel, which is a member of the expanded endocannabinoid system known as the endocannabinoidome (eCBome), counteract food intake and obesity. In this exploratory study, we examined the blood and stools from a subset of the participants in a cohort of reproductive-aged women with overweight/obesity who underwent a 12-week caloric restriction of 500 kcal/day with the administration of capsaicinoids (two capsules containing 100 mg of a capsicum annuum extract (CAE) each for a daily dose of 4 mg of capsaicinoids) or a placebo. Samples were collected immediately before and after the intervention, and plasma eCBome mediator levels (from 23 participants in total, 13 placebo and 10 CAE) and fecal microbiota taxa (from 15 participants in total, 9 placebo and 6 CAE) were profiled using LC–MS/MS and 16S metagenomic sequencing, respectively. CAE prevented the reduced caloric-intake-induced decrease in beneficial eCBome mediators, i.e., the TRPV1, GPR119 and/or PPARα agonists, N-oleoyl-ethanolamine, N-linoleoyl-ethanolamine and 2-oleoyl-glycerol, as well as the anti-inflammatory N-acyl-ethanolamines N-docosapentaenyl-ethanolamine and N-docosahexaenoyl-ethanolamine. CAE produced few but important alterations in the fecal microbiota, such as an increased relative abundance of the genus Flavonifractor, which is known to be inversely associated with obesity. Correlations between eCBome mediators and other potentially beneficial taxa were also observed, thus reinforcing the hypothesis of the existence of a link between the eCBome and the gut microbiome in obesity.

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19

Archambault, Anne-Sophie, Francesco Tinto, Élizabeth Dumais, Volatiana Rakotoarivelo, Magdalena Kostrzewa, Pier-Luc Plante, Cyril Martin, et al. "Biosynthesis of the Novel Endogenous 15-Lipoxygenase Metabolites N-13-Hydroxy-octodecadienoyl-ethanolamine and 13-Hydroxy-octodecadienoyl-glycerol by Human Neutrophils and Eosinophils." Cells 10, no. 9 (September 5, 2021): 2322. http://dx.doi.org/10.3390/cells10092322.

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The endocannabinoids 2-arachidonoyl-glycerol and N-arachidonoyl-ethanolamine are lipids regulating many physiological processes, notably inflammation. Endocannabinoid hydrolysis inhibitors are now being investigated as potential anti-inflammatory agents. In addition to 2-arachidonoyl-glycerol and N-arachidonoyl-ethanolamine, the endocannabinoidome also includes other monoacylglycerols and N-acyl-ethanolamines such as 1-linoleoyl-glycerol (1-LG) and N-linoleoyl-ethanolamine (LEA). By increasing monoacylglycerols and/or N-acyl-ethanolamine levels, endocannabinoid hydrolysis inhibitors will likely increase the levels of their metabolites. Herein, we investigated whether 1-LG and LEA were substrates for the 15-lipoxygenase pathway, given that both possess a 1Z,4Z-pentadiene motif, near their omega end. We thus assessed how human eosinophils and neutrophils biosynthesized the 15-lipoxygenase metabolites of 1-LG and LEA. Linoleic acid (LA), a well-documented substrate of 15-lipoxygenases, was used as positive control. N-13-hydroxy-octodecadienoyl-ethanolamine (13-HODE-EA) and 13-hydroxy-octodecadienoyl-glycerol (13-HODE-G), the 15-lipoxygenase metabolites of LEA and 1-LG, were synthesized using Novozym 435 and soybean lipoxygenase. Eosinophils, which express the 15-lipoxygenase-1, metabolized LA, 1-LG, and LEA into their 13-hydroxy derivatives. This was almost complete after five minutes. Substrate preference of eosinophils was LA > LEA > 1-LG in presence of 13-HODE-G hydrolysis inhibition with methyl-arachidonoyl-fluorophosphonate. Human neutrophils also metabolized LA, 1-LG, and LEA into their 13-hydroxy derivatives. This was maximal after 15–30 s. Substrate preference was LA ≫ 1-LG > LEA. Importantly, 13-HODE-G was found in humans and mouse tissue samples. In conclusion, our data show that human eosinophils and neutrophils metabolize 1-LG and LEA into the novel endogenous 15-lipoxygenase metabolites 13-HODE-G and 13-HODE-EA. The full biological importance of 13-HODE-G and 13-HODE-EA remains to be explored.

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20

Kuznetsova, T. A., M. U. Fereferov, and A. V. Pavshiskaya. "CLEANING GASOLINE THERMOCATALYTIC REFINING PROCESS SOLUTIONS OF ETHANOLAMINES." Scientific Papers Collection of the Angarsk State Technical University 1, no. 1 (2018): 17–20. http://dx.doi.org/10.36629/2686-7788-2018-1-1-17-20.

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21

Kuznecova, Tat'yana, Mihail Fereferov, and Anastasiya Pavshinskaya. "CLEANING GASOLINE THERMOCATALYTIC REFINING PROCESS SOLUTIONS OF ETHANOLAMINES." Scientific Papers Collection of the Angarsk State Technical University 2018, no. 1 (March 4, 2020): 17–20. http://dx.doi.org/10.36629/2686-7788-2018-1-17-20.

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The report considers the processes of purification of various petroleum products with solutions of monoethanolamine and presents the results of experiments on purification of catalytic cracking gasoline and gasoline fraction of diesel fuel hydrotreatment with solutions of monoethanolamine.

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22

Татьяна, Кузнецова, Mihail Fereferov, and Anastasiya Pavshinskaya. "CLEANING GASOLINE THERMOCATALYTIC REFINING PROCESS SOLUTIONS OF ETHANOLAMINES." Modern Technologies and Scientific and Technological Progress 2018, no. 1 (March 23, 2020): 21–22. http://dx.doi.org/10.36629/2686-9896-2020-2018-1-21-22.

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The report considers the processes of purification of various petroleum products with solutions of monoethanolamine and presents the results of experiments on purification of catalytic cracking gasoline and gasoline fraction of diesel fuel hydrotreatment with solutions of monoethanolamine.

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23

Cai, Zhenyun, Rongjing Xie, and Zhaoli Wu. "Binary Isobaric Vapor−Liquid Equilibria of Ethanolamines + Water." Journal of Chemical & Engineering Data 41, no. 5 (January 1996): 1101–3. http://dx.doi.org/10.1021/je960118o.

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24

PADHY, RANJAN KUMAR, and SREELEKHA DAS BHATTAMISRA. "Surfactant Catalyzed Oxidation of Ethanolamines by Cerium(IV)." Asian Journal of Chemistry 33, no. 1 (2020): 21–25. http://dx.doi.org/10.14233/ajchem.2021.22907.

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Effect of surfactant medium on the kinetics of oxidation of amino alcohol by cerium(IV) has been reported. Two amino alcohols namely, monoethanolamine (MEA) and triethanolamine (TEA) are chosen for kinetic study. Sizeable changes in reaction rate are noted only in presence of sodium lauryl sulphate (NaLS) as surfactant. Both the amino alcohols exhibit rate maxima at around the cmc of NaLS, beyond which the kψ-[NaLS] profile shows slow increase in rate constant with increasing NaLS concentration. Suitable model has been used to explain the kinetic pattern post CMC and from this the micelle-reactant binding constant values have been evaluated. From the temperature dependence study, the activation parameters for the oxidation reactions have been computed and these are compared against those obtained for aqueous medium. Based on all information, plausible mechanism for micellar catalysis has been presented.

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25

López-Rendón, Roberto, Marco A. Mora, José Alejandre, and Mark E. Tuckerman. "Molecular Dynamics Simulations of Aqueous Solutions of Ethanolamines." Journal of Physical Chemistry B 110, no. 30 (August 2006): 14652–58. http://dx.doi.org/10.1021/jp0619540.

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26

Herbig, Marcus, Lia Gevorgyan, Moritz Pflug, Jörg Wagler, Sandra Schwarzer, and Edwin Kroke. "CO 2 Capture with Silylated Ethanolamines and Piperazines." ChemistryOpen 9, no. 9 (December 11, 2019): 894–902. http://dx.doi.org/10.1002/open.201900269.

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27

Herbig, Marcus, Lia Gevorgyan, Moritz Pflug, Jörg Wagler, Sandra Schwarzer, and Edwin Kroke. "CO 2 Capture with Silylated Ethanolamines and Piperazines." ChemistryOpen 9, no. 9 (September 2020): 893. http://dx.doi.org/10.1002/open.202000212.

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28

Gangarapu, Satesh, Antonius T. M. Marcelis, Yahia A. Alhamed, and Han Zuilhof. "The Transition States for CO2Capture by Substituted Ethanolamines." ChemPhysChem 16, no. 14 (August 18, 2015): 3000–3006. http://dx.doi.org/10.1002/cphc.201500511.

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29

JIANG, Shaoliang, Jianrong GAO, and Liang HAN. "Synthesis and Biological Activity ofN-AcylO-Indolylalkyl Ethanolamines." Bioscience, Biotechnology, and Biochemistry 75, no. 4 (April 23, 2011): 768–70. http://dx.doi.org/10.1271/bbb.100804.

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30

Mukherjee, Partha, Sukalyan Dash, Sabita Patel, and Bijay K. Mishra. "Self-Organized Assemblies of Surfactants Derived from Ethanolamines." Journal of Dispersion Science and Technology 33, no. 6 (June 2012): 881–86. http://dx.doi.org/10.1080/01932691.2011.579827.

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31

Soares, Bruna P., Vojtěch Štejfa, Olga Ferreira, Simão P. Pinho, Květoslav Růžička, and Michal Fulem. "Vapor pressures and thermophysical properties of selected ethanolamines." Fluid Phase Equilibria 473 (October 2018): 245–54. http://dx.doi.org/10.1016/j.fluid.2018.05.032.

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32

Xhrouet, C�line, and Edwin De Pauw. "Prevention of dioxins de novo formation by ethanolamines." Environmental Chemistry Letters 1, no. 1 (March 1, 2003): 51–56. http://dx.doi.org/10.1007/s10311-002-0011-6.

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33

Leishman, Emma, Meera Manchanda, Rachel Thelen, Sally Miller, Ken Mackie, and Heather B. Bradshaw. "Cannabidiol's Upregulation of N-acyl Ethanolamines in the Central Nervous System Requires N-acyl Phosphatidyl Ethanolamine-Specific Phospholipase D." Cannabis and Cannabinoid Research 3, no. 1 (November 2018): 228–41. http://dx.doi.org/10.1089/can.2018.0031.

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34

Malewicz, Barbara, Jagat J. Mukherjee, Karan S. Crilly, Wolfgang J. Baumann, and Zoltan Kiss. "Phosphorylation of ethanolamine, methylethanolamine, and dimethylethanolamine by overexpressed ethanolamine kinase in NIH 3T3 cells decreases the co-mitogenic effects of ethanolamines and promotes cell survival." European Journal of Biochemistry 253, no. 1 (April 1998): 10–19. http://dx.doi.org/10.1046/j.1432-1327.1998.2530010.x.

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35

Cherton, J. C., S. Hamm, J. C. Hallé, L. Menguy, and M. Beaufour. "Potential proinsecticides of fluorinated carboxylic acids and β-ethanolamines." Journal of Fluorine Chemistry 107, no. 2 (February 2001): 387–95. http://dx.doi.org/10.1016/s0022-1139(00)00382-1.

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36

Rahman, Mahmud A., Robert N. Maddox, and G. J. Mains. "Reactions of carbonyl sulfide and methyl mercaptan with ethanolamines." Industrial & Engineering Chemistry Research 28, no. 4 (April 1989): 470–75. http://dx.doi.org/10.1021/ie00088a014.

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37

Chen, Ling, Liya Yang, Chunxia Wang, and Ting Zhu. "Reactivity of Metal Boronhydride Derivatives with Amines and Ethanolamines." IOP Conference Series: Materials Science and Engineering 772 (March 31, 2020): 012036. http://dx.doi.org/10.1088/1757-899x/772/1/012036.

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38

Kim, Shin-bum, Chung-sik Yoon, and Donguk Park. "Vaporization and Conversion of Ethanolamines used in Metalworking Operations." Safety and Health at Work 1, no. 2 (December 2010): 175–82. http://dx.doi.org/10.5491/shaw.2010.1.2.175.

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39

Fustero, Santos, Ana C. Cuñat, Sonia Flores, Claribel Báez, Judit Oliver, Michael Cynamon, Michael Gütschow, et al. "Design, Synthesis, and Biological Evaluation of Novel Fluorinated Ethanolamines." Chemistry - A European Journal 17, no. 52 (November 24, 2011): 14772–84. http://dx.doi.org/10.1002/chem.201102078.

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40

Dolphen, R., and P. Thiravetyan. "Phytodegradation of Ethanolamines byCyperus alternifolius: Effect of Molecular Size." International Journal of Phytoremediation 17, no. 7 (May 15, 2015): 686–92. http://dx.doi.org/10.1080/15226514.2014.964839.

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41

Horikoshi, Satoshi, Natsuko Watanabe, Miki Mukae, Hisao Hidaka, and Nick Serpone. "Mechanistic examination of the titania photocatalyzed oxidation of ethanolamines." New Journal of Chemistry 25, no. 8 (2001): 999–1005. http://dx.doi.org/10.1039/b102186i.

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42

Estrin, Ya I., V. V. Komratova, G. A. Estrina, V. P. Lodygina, and B. A. Rozenberg. "Selectivity of acylation of ethanolamines with (meth)acryloyl chlorides." Russian Journal of Applied Chemistry 81, no. 1 (January 2008): 135–43. http://dx.doi.org/10.1134/s1070427208010308.

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43

Han, Hyo-Kyung, and Hoo-Kyun Choi. "Improved absorption of meloxicam via salt formation with ethanolamines." European Journal of Pharmaceutics and Biopharmaceutics 65, no. 1 (January 2007): 99–103. http://dx.doi.org/10.1016/j.ejpb.2006.07.003.

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44

Rozsypal, Tomas. "Development of a method for derivatization of ethanolamines and its application to sand samples." Journal of the Serbian Chemical Society, no. 00 (2021): 47. http://dx.doi.org/10.2298/jsc210312047r.

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Nitrogen mustards are dangerous and available blistering chemical warfare agents. In the presented study, six derivatization methods are compared for the analysis of degradation products of the most important blistering nitrogen mustards (ethyl diethanolamine, methyl diethanolamine and triethanolamine) by gas chromatography coupled with mass spectrometry. Five silylation methods (using BSTFA and BSA) and one trifluoroacetylation method (using TFAA) were tested. The derivatization reactions were performed in acetonitrile. As the method with optimal results, trifluoroacetylation by TFAA was selected. Analytes reacted with the corresponding reagent rapidly, quantitatively, with stable kinetics and at room temperature. Calibration curves for quantitative analysis of ethanolamines after TFAA derivatization were created. Correspond-ing detection limits varied between 9?10-3 and 7?10-5 mmol?dm-3 for the tested analytes. The developed method was applied for the analysis of ethanolamines after extraction from sand using acetonitrile. Limits of detection were 11.4 to 12.3 ?g of the analyte in 1 g of sand. It is encouraged to use the developed method in military deployable laboratories designated for rapid identification of chemical warfare agents and corresponding degradation products.

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45

Fouda, A. S., M. Abdallah, I. S. Ahmed, and M. Eissa. "Corrosion inhibition of aluminum in 1M H3PO4 solutions by ethanolamines." Arabian Journal of Chemistry 5, no. 3 (July 2012): 297–307. http://dx.doi.org/10.1016/j.arabjc.2010.08.020.

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46

Sivakumar, Aathimanivelu V., Anand M. Lahoti, and Sujata V. Bhat. "Enantioselective Synthesis of Phenyl-ethanolamines Through Application of Chiral Sulfoxide." Synthetic Communications 39, no. 18 (August 12, 2009): 3338–47. http://dx.doi.org/10.1080/00397910902765578.

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47

Maslennikov, Aleksandr, Ilya Zubkov, and Nikolai Peskov. "Technological concentration sensor for ethanolamines based on an optical sensor." MATEC Web of Conferences 212 (2018): 01028. http://dx.doi.org/10.1051/matecconf/201821201028.

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The most important parameters necessary for the precise control of the separation of monoethanolamine, diethanolamine, and triethanolamine on column distillation apparatus are their initial concentrations in the mixtures fed to the columns. Currently, the use of a solid-state optical sensor, which makes it possible to determine the desired ratio in a mode close to the real-time regime. The technical parameters for the sensitivity and speed achieved by the sensor are determined in the determination of monoethanolamine, diethanolamine, and triethanolamine, as well as the sensor parameters and conditions of use, which enable the sensor to effectively solve the tasks. In particular, the concentration of the mixture of analytes in the sensor chamber is 500 mg / m3, the thickness of the sensitive coating is about 0.5 μm, the operating temperature is 45÷50 ° C, the time for one cycle of measuring the diethanolamine/triethanolamine ratio is 150 ÷ 180 seconds.

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48

Mcguigan, Christopher, and Bernadette Swords. "A High Yield Synthesis of Phosphatidyl Ethanolamines Using Phosphoramidite Intermediates." Synthesis 1993, no. 01 (1993): 133–36. http://dx.doi.org/10.1055/s-1993-25816.

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49

Kapteina, Simon, Krzysztof Slowik, Sergey P. Verevkin, and Andreas Heintz. "Vapor Pressures and Vaporization Enthalpies of a Series of Ethanolamines." Journal of Chemical & Engineering Data 50, no. 2 (March 2005): 398–402. http://dx.doi.org/10.1021/je049761y.

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50

Hancock, Jared M., William M. Rankin, Brielle Woolsey, Reagan S. Turley, and Roger G. Harrison. "Controlled formation of ZnO hexagonal prisms using ethanolamines and water." Journal of Sol-Gel Science and Technology 84, no. 1 (August 24, 2017): 214–21. http://dx.doi.org/10.1007/s10971-017-4486-9.

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