Добірка наукової літератури з теми "Esterification Reactivity"
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Статті в журналах з теми "Esterification Reactivity"
Zhan, Shaoqi, Xiaochun Tao, Liangzhen Cai, Xiaohui Liu, and Taoping Liu. "The carbon material functionalized with NH2+ and SO3H groups catalyzed esterification with high activity and selectivity." Green Chem. 16, no. 11 (2014): 4649–53. http://dx.doi.org/10.1039/c4gc01395f.
Повний текст джерелаMei, Sheng-Fu, Jin Liu, Zhen Li, Yan Chen, and Jing Zhang. "Reactivity of 2-Phosphonobutane-1,2,4-tricarboxylic Acid Esterification." Asian Journal of Chemistry 26, no. 5 (2014): 1530–32. http://dx.doi.org/10.14233/ajchem.2014.17279.
Повний текст джерелаLi, Chong, Yueping Jiang, Baoshan Huang, Menghang Zhang, Yanhong Feng, and Zhitao Yang. "Preparation and Properties of Jute Fiber Long-Chain Fatty Acid Esters in Supercritical Carbon Dioxide." Materials 12, no. 9 (May 8, 2019): 1499. http://dx.doi.org/10.3390/ma12091499.
Повний текст джерелаRoswanda, Robby, Ilham Ardatul Putra, Maria Mardiastuti, and Didin Mujahidin. "Catalyst Free Hydroxyl Protection of Quinine via Esterification." Key Engineering Materials 811 (July 2019): 3–7. http://dx.doi.org/10.4028/www.scientific.net/kem.811.3.
Повний текст джерелаKastratović, Vlatko, Milica Radulović, and Kristina Kastratović. "Esterification of propanoic acid in the presence of a homogeneous catalyst." Kragujevac Journal of Science, no. 44 (2022): 45–55. http://dx.doi.org/10.5937/kgjsci2244045k.
Повний текст джерелаVázquez, Ester, and Maurizio Prato. "Functionalization of carbon nanotubes for applications in materials science and nanomedicine." Pure and Applied Chemistry 82, no. 4 (March 13, 2010): 853–61. http://dx.doi.org/10.1351/pac-con-09-10-40.
Повний текст джерелаWu, Yan, Shiang He, Dongmei Li, Yang Li, and Hao Wang. "Esterification of naphthenic acids with various structures over tungstophosphoric acid-intercalated layer double hydroxide catalysts with various interlayer spacings." Clay Minerals 56, no. 3 (September 2021): 250–59. http://dx.doi.org/10.1180/clm.2022.3.
Повний текст джерелаKastratovic, Vlatko, and Miljan Bigovic. "Esterification of stearic acid with lower monohydroxylic alcohols." Chemical Industry and Chemical Engineering Quarterly 24, no. 3 (2018): 283–91. http://dx.doi.org/10.2298/ciceq170327040k.
Повний текст джерелаBreitenlechner, Stefan, and Thorsten Bach. "Kinetic Study on the Esterification of Hexanoic Acid with N,N-Dialkylamino Alcohols: Evidence for an Activation by Hydrogen Bonding." Zeitschrift für Naturforschung B 61, no. 5 (May 1, 2006): 583–88. http://dx.doi.org/10.1515/znb-2006-0513.
Повний текст джерелаRabee, Abdallah, Gamal Mekhemer, Amin Osatiashtiani, Mark Isaacs, Adam Lee, Karen Wilson, and Mohamed Zaki. "Acidity-Reactivity Relationships in Catalytic Esterification over Ammonium Sulfate-Derived Sulfated Zirconia." Catalysts 7, no. 7 (July 5, 2017): 204. http://dx.doi.org/10.3390/catal7070204.
Повний текст джерелаДисертації з теми "Esterification Reactivity"
Eberhardt, Nathan A. "Synthesis and Reactivity of Nickel POCOP Pincer Complexes for the Reduction of Carbon Dioxide and Related Compounds." University of Cincinnati / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1511864001952451.
Повний текст джерелаLegoupy, Stéphanie. "Synthèse et réactivité de nouveaux complexes organométalliques chiraux du rhénium." Rennes 1, 1997. http://www.theses.fr/1997REN10148.
Повний текст джерелаYang, Chiehju, and 楊捷如. "Preparation of Sulfated Magnetic Solid Acid Catalyst (SO42−/ Sr7Fe10O22) with Highly Catalytic Reactivity for the Esterification of Oleic Acid and Methanol." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/bvpcdu.
Повний текст джерела靜宜大學
化粧品科學系
101
Transesterification and esterification are the main routes for obtaining esters from plant oils and fatty acids, respectively. Nowadays, these two reactions are catalyzed by homogeneous catalysts (inorganic base or acid) in industry. However, the use of homogeneous catalyst in ester production has serious drawbacks associated with separation, catalyst regeneration and acid/base contamination in the product. Solid catalysts are the promising alternative to homogeneous catalysts. In this work, we focused on the development of solid acid catalyst for the production of esters because the application of solid base catalysts in the production of ester is limited by their low tolerance for the fatty acids containing in natural plant oils. A series of SO42−/M-Fe2O3 (M; doped metal ion in magnetic particle) catalysts were synthesized, and their catalytic abilities were examined in the esterification of oleic acid and methanol at 100°C. The desired metal ions (M) were incorporated in the magnetic support by co-precipitation method. Sulfite groups are then grafted onto the support surface by immersing the support into H2SO4 aqueous solution at a moderate temperature. The physiochemical properties of SO42−/M-Fe2O3 catalysts were characterized by Scanning Electron Microscopy(SEM), X-ray Diffraction(XRD), Brunauer-Emmett-Teller method(BET), Fourier-Transform Infrared Spectrometer(FT-IR) and Hammett Indicators, separately. The results show that the catalysts feature extremely high catalytic reactivity for the esterification in comparison with homogeneous acid catalysts or the solid catalysts reported in the literature. When the esterification of oleic acid with methanol (molar ratio 1:4) was conducted at 100oC in the presence of 10 wt% SO42−/ Sr7Fe10O22, the conversion of oleic acid was over than 95% after 2 hour of the reaction. Heat-treating the used catalyst at 400oC for 1 hours is helpful to recover 85% activity of SO42−/Sr7Fe10O22, and the IR spectrum of used SO42−/Sr7Fe10O22 indicated that the inactivation of SO42−/Sr7Fe10O22, mainly derived from the adsorption of product (oleic acid methyl ester) or reagent (oleic acid) on the active sites.
Частини книг з теми "Esterification Reactivity"
Frey, Perry A., and Adrian D. Hegeman. "Alkyltransferases." In Enzymatic Reaction Mechanisms. Oxford University Press, 2007. http://dx.doi.org/10.1093/oso/9780195122589.003.0019.
Повний текст джерелаТези доповідей конференцій з теми "Esterification Reactivity"
John, George, Jose James, Malick Samateh, Siddharth Marwaha, and Vikas Nanda. "Sucralose Hydrogels: Peering into the Reactivity of Sucralose versus Sucrose Using Lipase Catalyzed Trans-Esterification." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/xkza4963.
Повний текст джерела