Статті в журналах з теми "Organic eutectics"
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Rai, Uma Shanker, Manjeet Singh, and Rama Nand Rai. "Crystal growth and some physicochemical studies on an organic intermolecular compound of anthranilic acid and N,N-dimethylamino benzaldehyde." European Journal of Chemistry 9, no. 4 (December 31, 2018): 303–10. http://dx.doi.org/10.5155/eurjchem.9.4.303-310.1720.
Повний текст джерелаYoshikawa, Shinichi, Shimpei Watanabe, Yoshinori Yamamoto, and Fumitoshi Kaneko. "Binary Phase Behavior of 1,3-Distearoyl-2-oleoyl-sn-glycerol (SOS) and Trilaurin (LLL)." Molecules 25, no. 22 (November 14, 2020): 5313. http://dx.doi.org/10.3390/molecules25225313.
Повний текст джерелаAraya-Sibaja, Andrea, José Vega-Baudrit, Teodolito Guillén-Girón, Mirtha Navarro-Hoyos, and Silvia Cuffini. "Drug Solubility Enhancement through the Preparation of Multicomponent Organic Materials: Eutectics of Lovastatin with Carboxylic Acids." Pharmaceutics 11, no. 3 (March 9, 2019): 112. http://dx.doi.org/10.3390/pharmaceutics11030112.
Повний текст джерелаGupta, R. K., S. K. Singh, and R. A. Singh. "Some physicochemical studies on organic eutectics." Journal of Crystal Growth 300, no. 2 (March 2007): 415–20. http://dx.doi.org/10.1016/j.jcrysgro.2006.12.017.
Повний текст джерелаRai, U. S., and K. D. Mandal. "Some physicochemical studies on organic eutectics and 1:1 addition compound; p-phenylenediamine – benzoic acid system." Canadian Journal of Chemistry 67, no. 2 (February 1, 1989): 239–44. http://dx.doi.org/10.1139/v89-039.
Повний текст джерелаNahar, Yeasmin, and Stuart C. Thickett. "Greener, Faster, Stronger: The Benefits of Deep Eutectic Solvents in Polymer and Materials Science." Polymers 13, no. 3 (January 30, 2021): 447. http://dx.doi.org/10.3390/polym13030447.
Повний текст джерелаPramanik, Titas, Ashish Anand, Janaky Sunil, Anjana Joseph, Chandrabhas Narayana, Somnath Dutta, and Tayur N. Guru Row. "Organic eutectics: characterization, microstructural evolution and properties." Acta Crystallographica Section A Foundations and Advances 77, a2 (August 14, 2021): C121. http://dx.doi.org/10.1107/s0108767321095593.
Повний текст джерелаRai, U. S., and H. Shekhar. "Some physicochemical studies on binary organic eutectics." Thermochimica Acta 175, no. 2 (March 1991): 215–27. http://dx.doi.org/10.1016/0040-6031(91)80068-t.
Повний текст джерелаRai, U. S., and Santhi George. "A physicochemical study on organic eutectics and addition compound; benzidine–pyrogallol system." Canadian Journal of Chemistry 70, no. 12 (December 1, 1992): 2869–74. http://dx.doi.org/10.1139/v92-366.
Повний текст джерелаAlhadid, Ahmad, Liudmila Mokrushina, and Mirjana Minceva. "Design of Deep Eutectic Systems: A Simple Approach for Preselecting Eutectic Mixture Constituents." Molecules 25, no. 5 (February 28, 2020): 1077. http://dx.doi.org/10.3390/molecules25051077.
Повний текст джерелаRai, U. S., and K. D. Mandal. "Solidification Behaviour of Organic Eutectics and Addition Compounds." Materials Science Forum 50 (January 1991): 117–28. http://dx.doi.org/10.4028/www.scientific.net/msf.50.117.
Повний текст джерелаRai, U. S., K. D. Mandal, and N. P. Singh. "Thermochemical studies on organic eutectics and molecular complexes." Journal of Thermal Analysis 35, no. 5 (September 1989): 1687–97. http://dx.doi.org/10.1007/bf01912943.
Повний текст джерелаSharma, Krishna, Prakash Ghimire, and Umesh Neupane. "Solid-Liquid Equilibrium Study for Binary System Forming Intermolecular Compound: Phase Diagram, Thermal, Physicochemical and Powder XRD study." Journal of Nepal Chemical Society 43, no. 1 (August 30, 2022): 1–3. http://dx.doi.org/10.3126/jncs.v43i1.46956.
Повний текст джерелаRai, U. S., and R. N. Rai. "Some Physicochemical Studies on Organic Eutectics and Molecular Complex: Urea – p-nitrophenol System." Journal of Materials Research 14, no. 4 (April 1999): 1299–305. http://dx.doi.org/10.1557/jmr.1999.0177.
Повний текст джерелаRai, U. S., Manjeet Singh, and R. N. Rai. "Some physicochemical studies on organic eutectics and inter-molecular compounds." Journal of Thermal Analysis and Calorimetry 130, no. 2 (May 8, 2017): 967–74. http://dx.doi.org/10.1007/s10973-017-6429-7.
Повний текст джерелаGupta, R. K., and R. A. Singh. "Thermochemical and microstructural studies on binary organic eutectics and complexes." Journal of Crystal Growth 267, no. 1-2 (June 2004): 340–47. http://dx.doi.org/10.1016/j.jcrysgro.2004.03.025.
Повний текст джерелаReddi, R. S. B., V. S. A. Kumar Satuluri, and R. N. Rai. "Solid–liquid equilibrium, thermal and physicochemical studies of organic eutectics." Journal of Thermal Analysis and Calorimetry 107, no. 1 (May 21, 2011): 183–88. http://dx.doi.org/10.1007/s10973-011-1634-2.
Повний текст джерелаRai, U. S., and R. N. Rai. "Some Physicochemical Studies on Organic Analog of Metal-Nonmetal Eutectics." Crystal Research and Technology 32, no. 6 (1997): 821–29. http://dx.doi.org/10.1002/crat.2170320614.
Повний текст джерелаRai, U. S., and K. D. Mandal. "Some Physicochemical Studies on Organic Eutectics and 1:2 Addition Compounds." Molecular Crystals and Liquid Crystals 182, no. 1 (May 1, 1990): 387–404. http://dx.doi.org/10.1080/00268949008035768.
Повний текст джерелаChapman, Robert D., and John W. Fronabarger. "A Convenient Correlation for Prediction of Binary Eutectics Involving Organic Explosives." Propellants, Explosives, Pyrotechnics 23, no. 1 (February 1998): 50–55. http://dx.doi.org/10.1002/(sici)1521-4087(199802)23:1<50::aid-prep50>3.0.co;2-e.
Повний текст джерелаKaur, Ramanpreet, Raj Gautam, Suryanarayan Cherukuvada, and Tayur N. Guru Row. "Do carboximide–carboxylic acid combinations form co-crystals? The role of hydroxyl substitution on the formation of co-crystals and eutectics." IUCrJ 2, no. 3 (April 10, 2015): 341–51. http://dx.doi.org/10.1107/s2052252515002651.
Повний текст джерелаDorset, Douglas L. "Crystal structure of lamellar paraffin eutectics." Macromolecules 19, no. 12 (December 1986): 2965–73. http://dx.doi.org/10.1021/ma00166a015.
Повний текст джерелаDolotko, Oleksandr, Jerzy W. Wiench, Kevin W. Dennis, Vitalij K. Pecharsky, and Viktor P. Balema. "Mechanically induced reactions in organic solids: liquid eutectics or solid-state processes?" New J. Chem. 34, no. 1 (2010): 25–28. http://dx.doi.org/10.1039/b9nj00588a.
Повний текст джерелаRai, U. S., and H. Shekhar. "Chemistry of Binary Organic Eutectics and Molecular Complexes: Phenanthrenem. Nitrobenzoic Acid System." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 220, no. 1 (September 1992): 217–30. http://dx.doi.org/10.1080/10587259208033442.
Повний текст джерелаRai, U. S., and H. Shekhar. "Chemistry of organic eutectics: Phenanthrene — benzoic acid and phenanthrene — cinnamic acid systems." Crystal Research and Technology 25, no. 7 (July 1990): 771–79. http://dx.doi.org/10.1002/crat.2170250708.
Повний текст джерелаRai, U. S., and Santhi George. "Some Physicochemical Studies on Binary Organic Eutectics and 1:2 Molecular Complexes." Crystal Research and Technology 26, no. 4 (1991): 511–19. http://dx.doi.org/10.1002/crat.2170260426.
Повний текст джерелаDorset, Douglas L., James Hanlon, and Gail Karet. "Epitaxy and structure of paraffin-diluent eutectics." Macromolecules 22, no. 5 (September 1989): 2169–76. http://dx.doi.org/10.1021/ma00195a029.
Повний текст джерелаRai, U. S., and K. D. Mandal. "Chemistry of organic eutectics and 1:1 addition compound: p-phenylenediamine-catechol system." Thermochimica Acta 138, no. 2 (February 1989): 219–31. http://dx.doi.org/10.1016/0040-6031(89)87258-2.
Повний текст джерелаRai, U. S., and Pinky Pandey. "Solidification behaviour of binary organic eutectics and monotectics; 1,2,4,5-tetrachlorobenzene–m-aminophenol system." Materials Letters 39, no. 3 (May 1999): 166–72. http://dx.doi.org/10.1016/s0167-577x(98)00235-3.
Повний текст джерелаKaul, Michael J., Diab Qadah, Victoria Mandella, and Mark L. Dietz. "Systematic evaluation of hydrophobic deep-melting eutectics as alternative solvents for the extraction of organic solutes from aqueous solution." RSC Advances 9, no. 28 (2019): 15798–804. http://dx.doi.org/10.1039/c9ra01596e.
Повний текст джерелаPandey, Saurabh, Abhishek Anand, Dharam Buddhi, and Atul Sharma. "Development and thermophysical analysis of binary eutectics phase change materials for solar drying application." F1000Research 11 (November 9, 2022): 1277. http://dx.doi.org/10.12688/f1000research.127268.1.
Повний текст джерелаRai, U. S., and K. D. Mandal. "Solidification behaviour of organic eutectics and 1:1 addition compound: p-Phenylenediamine-resorcinol system." Crystal Research and Technology 23, no. 7 (July 1988): 871–80. http://dx.doi.org/10.1002/crat.2170230706.
Повний текст джерелаRai, U. S., та Santhi George. "Some physicochemical studies on organic eutectics and 1:2 addition compound; benzidine-β-naphthol system". Thermochimica Acta 191, № 2 (грудень 1991): 271–84. http://dx.doi.org/10.1016/0040-6031(91)87219-m.
Повний текст джерелаRai, U. S., та Santhi George. "Physicochemical studies on organic eutectics and the 1:1 addition compound: benzidine-α-naphthol system". Journal of Materials Science 27, № 3 (лютий 1992): 711–18. http://dx.doi.org/10.1007/bf02403884.
Повний текст джерелаAdeel Hassan, Hafiz Muhammad, and Ivar Lund. "Inorganic PCMs applications in passive cooling of buildings - A review." Journal of Physics: Conference Series 2116, no. 1 (November 1, 2021): 012103. http://dx.doi.org/10.1088/1742-6596/2116/1/012103.
Повний текст джерелаRai, U. S., and R. N. Rai. "Chemistry and characterization of binary organic eutectics and molecular complexes. The urea-m-nitrobenzoic acid system." Materials Letters 34, no. 1-2 (February 1998): 67–75. http://dx.doi.org/10.1016/s0167-577x(97)00147-x.
Повний текст джерелаRai, U. S. "Some physicochemical studies on binary organic eutectics and 1:1 addition compound; benzidine-p-nitrophenol system." Journal of Crystal Growth 144, no. 3-4 (December 1994): 291–96. http://dx.doi.org/10.1016/0022-0248(94)90469-3.
Повний текст джерелаCorset, D. L. "Crystal Structure Analysis of Organic Solid Solutions and Eutectics in the Electron Microscope: Paraffins, Polymers and Lipids." Solid State Phenomena 5 (January 1989): 185–0. http://dx.doi.org/10.4028/www.scientific.net/ssp.5.185.
Повний текст джерелаFernandes, Richard Perosa, Ana Carina Sobral de Carvalho, Bruno Ekawa, Andre Luiz Soares Carneiro do Nascimento, Andressa Maria Pironi, Marlus Chorilli, and Flávio Junior Caires. "Synthesis and characterization of meloxicam eutectics with mandelic acid and saccharin for enhanced solubility." Drug Development and Industrial Pharmacy 46, no. 7 (June 12, 2020): 1092–99. http://dx.doi.org/10.1080/03639045.2020.1775633.
Повний текст джерелаCysewski, Piotr, Tomasz Jeliński, Patryk Cymerman, and Maciej Przybyłek. "Solvent Screening for Solubility Enhancement of Theophylline in Neat, Binary and Ternary NADES Solvents: New Measurements and Ensemble Machine Learning." International Journal of Molecular Sciences 22, no. 14 (July 8, 2021): 7347. http://dx.doi.org/10.3390/ijms22147347.
Повний текст джерелаZhang, W. P., and D. L. Dorset. "Direct lattice imaging of domain boundaries in N-paraffin binary eutectics formed from the vapor phase." Proceedings, annual meeting, Electron Microscopy Society of America 47 (August 6, 1989): 702–3. http://dx.doi.org/10.1017/s0424820100155487.
Повний текст джерелаSingh, N. P., B. M. Shukla, Namwar Singh, and Narsingh Bahadur Singh. "Structure of melts in binary organic eutectics and molecular complexes. Phenanthrene-picric acid and anthracene-picric acid systems." Journal of Chemical & Engineering Data 30, no. 1 (January 1985): 49–50. http://dx.doi.org/10.1021/je00039a016.
Повний текст джерелаMatsumoto, Shogen, Shunsuke Kurosawa, Daisaku Yokoe, Teiichi Kimura, and Akihiko Ito. "Growth and scintillation properties of Ce 3+:LuAG–Al2O3 chemically deposited eutectics." Optical Materials 138 (April 2023): 113674. http://dx.doi.org/10.1016/j.optmat.2023.113674.
Повний текст джерелаAhmad, Naveed, Xingyu Lin, Xiaoxiao Wang, Jian Xu, and Xia Xu. "Understanding the CO2 capture performance by MDEA-based deep eutectics solvents with excellent cyclic capacity." Fuel 293 (June 2021): 120466. http://dx.doi.org/10.1016/j.fuel.2021.120466.
Повний текст джерелаSudheer, R., and K. Narayan Prabhu. "Characterization of Metal-PCMs for Thermal Energy Storage Applications." Materials Science Forum 830-831 (September 2015): 505–8. http://dx.doi.org/10.4028/www.scientific.net/msf.830-831.505.
Повний текст джерелаAlkhawaja, Bayan, Faisal Al-Akayleh, Ashraf Al-Khateeb, Jehad Nasereddin, Bayan Y. Ghanim, Albert Bolhuis, Nisrein Jaber, Mayyas Al-Remawi, and Nidal A. Qinna. "Deep Eutectic Liquids as a Topical Vehicle for Tadalafil: Characterisation and Potential Wound Healing and Antimicrobial Activity." Molecules 28, no. 5 (March 6, 2023): 2402. http://dx.doi.org/10.3390/molecules28052402.
Повний текст джерелаSaeed, Zeinab M., Bhausaheb Dhokale, Abeer F. Shunnar, Wegood M. Awad, Hector H. Hernandez, Panče Naumov, and Sharmarke Mohamed. "Crystal Engineering of Binary Organic Eutectics: Significant Improvement in the Physicochemical Properties of Polycyclic Aromatic Hydrocarbons via the Computational and Mechanochemical Discovery of Composite Materials." Crystal Growth & Design 21, no. 7 (June 15, 2021): 4151–61. http://dx.doi.org/10.1021/acs.cgd.1c00420.
Повний текст джерелаBRUNET, L., J. CAILLARD, and P. ANDRÉ. "THERMODYNAMIC CALCULATION OF n-COMPONENT EUTECTIC MIXTURES." International Journal of Modern Physics C 15, no. 05 (June 2004): 675–87. http://dx.doi.org/10.1142/s0129183104006121.
Повний текст джерелаPodolinsky, V. V., Yu N. Taran, and V. G. Drykin. "Eutectic solidification in organic systems." Journal of Crystal Growth 74, no. 1 (January 1986): 57–66. http://dx.doi.org/10.1016/0022-0248(86)90248-4.
Повний текст джерелаThakur, Ajay, Monika Verma, Ruchi Bharti, and Renu Sharma. "Recent Advances in Utilization of Deep Eutectic Solvents: An Environmentally Friendly Pathway for Multi-component Synthesis." Current Organic Chemistry 26, no. 3 (February 2022): 299–323. http://dx.doi.org/10.2174/1385272826666220126165925.
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