J
J.M. Létoffé
Researcher at Intelligence and National Security Alliance
Publications - 8
Citations - 164
J.M. Létoffé is an academic researcher from Intelligence and National Security Alliance. The author has contributed to research in topics: Differential scanning calorimetry & Thermal analysis. The author has an hindex of 6, co-authored 8 publications receiving 161 citations.
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Journal ArticleDOI
Thermal behaviour of hydrated and anhydrous Cucurbituril: A DSC, T.G. and calorimetric study in temperature range from 100 to 800 K
TL;DR: In this article, the enthalpy of differently hydrated Cucurbituril samples was studied using Differential Scanning Calorimetry and Thermogravimetry in the temperature range from 100 to 800 K.
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Physicochemical characterization of cholesterol-beta cyclodextrin inclusion complexes
TL;DR: In this article, a stable hydrate between cholesterol and β cyclodextrin (βCD) was characterized using X-ray diffraction, thermogravimetric analysis (TG), differential scanning calorimetry (DSC), and nuclear magnetic resonance spectroscopy (13C NMR).
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Action des molecules organiques sur les composes d'insertion de metaux alcalins dans le graphite
TL;DR: Les bases de Lewis (Tetrahydrofuranne, Dimethyl-2,5 tetrahedrofuraine, Dimethoxyethane,Dimethyl ether du triethylene glycol, Dioxanne, Triethylamine, N,N,N N′,N′ tetramethyl ethylene diamine) penetrent dans les composes d'insertion de metaux alcalins dans le graphite (LiC12, KC36).
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Thermal characteristics of crude oils treated with rheology modifiers
TL;DR: In this paper, the authors studied the thermal characteristics of eight crude oils and their treatment with additives by differential scanning calorimetry (DSC), thermomicroscopy, viscometer and pour point tester.
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Physico-chemical characterization of base stocks and thermal analysis by differential scanning calorimetry and thermomicroscopy at low temperature
TL;DR: In this paper, differential scanning calorimetry (DSC) is used for characterization of the thermal behavior of lubricating oils, allowing the determination of crystallization temperature and amount of precipitated fractions versus temperature.