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11.
Tin oxide nanophases or nanoparticles were synthesized under conventional- and microwave-hydrothermal conditions and characterized by powder X-ray diffraction, BET surface area determination as well as transmission electron microscopy. The use of microwave-hydrothermal (M-H) process led to higher yields in shorter time compared to the conventional-hydrothermal (C-H) process because of increased reaction rates in the former. 相似文献
12.
Dr. Pierre-Yves Geant Dr. Malika Kaci Dr. Jean-Pierre Uttaro Prof. Christian Périgaud Prof. Christophe Mathé 《ChemMedChem》2019,14(5):522-526
The synthesis and anti-HIV evaluation of hitherto unknown 3′-fluoro-5′-norcarbocyclic nucleoside phosphonates bearing adenine with modifications at the 4′ position (ethynyl, vinyl, ethyl, hydroxymethyl) is described. One of the synthesized compounds was found to be an inhibitor of HIV-1 replication, but with moderate efficiency relative to (R)-9-(2-phosphonylmethoxypropyl)adenine ((R)-PMPA, tenofovir), with no concomitant cytotoxicity. 相似文献
13.
This paper presents the results of a study which has been carried out to investigate the crevice corrosion behavior of high-alloy stainless steel in a SWRO pilot plant. The study evaluated the corrosion performance of some austenitic and duplex steels in a crevice-forming environment created in a RO plant, especially in high-pressure feed and brine lines. The study of the effect of chemical dosing on crevice corrosion in the RO plant and electrochemical testing of crevice corrosion in the laboratory were the main objectives of this test program. High-alloy stainless steels, namely AL 6XN® and 254 SMO (superaustenitic), 2205, 2507 and DP3W (Duplex) were used in the test program. The tests were carried out in natural seawater and RO concentrate (conductivity: 75,000 to 80,000 μS/cm) at ambient temperature by operating the test plant at normal SWRO operating feed pressure of 54 bar. FeCl3 was added as coagulant to maintain a silt density index of ∼3, and H2SO4 was added to feed in order to maintain the feed pH of ∼ 6.5. Chlorination and subsequent dechlorination agents were not added to the feed. For crevice corrosion tests in RO unit, the exposure periods were 6 and 12 months, respectively. The results of the tests showed that alloy DP3W has the best pitting resistance in crevice forming environment of seawater. In RO concentrate, alloys 2507 and 254 SMO showed lowest “maximum pit depth”. The results of potentiodynamic cyclic polarization (PCP) indicate that all the alloys have high pitting potential and small hysteresis loop. The results of critical crevice solution pH (CCSpH) indicated excellent resistance of alloys 254 SMO and DP3W against crevice corrosion attack and 2205 had least resistance in most aggressive sodium chloride solution. 相似文献
14.
Li B Sauvé G Iovu MC Jeffries-El M Zhang R Cooper J Santhanam S Schultz L Revelli JC Kusne AG Kowalewski T Snyder JL Weiss LE Fedder GK McCullough RD Lambeth DN 《Nano letters》2006,6(8):1598-1602
Regioregular polythiophene-based conductive copolymers with highly crystalline nanostructures are shown to hold considerable promise as the active layer in volatile organic compound (VOC) chemresistor sensors. While the regioregular polythiophene polymer chain provides a charge conduction path, its chemical sensing selectivity and sensitivity can be altered either by incorporating a second polymer to form a block copolymer or by making a random copolymer of polythiophene with different alkyl side chains. The copolymers were exposed to a variety of VOC vapors, and the electrical conductivity of these copolymers increased or decreased depending upon the polymer composition and the specific analytes. Measurements were made at room temperature, and the responses were found to be fast and appeared to be completely reversible. Using various copolymers of polythiophene in a sensor array can provide much better discrimination to various analytes than existing solid state sensors. Our data strongly indicate that several sensing mechanisms are at play simultaneously, and we briefly discuss some of them. 相似文献
15.
Lahiani-Skiba M Barbot C Bounoure F Joudieh S Skiba M 《Drug development and industrial pharmacy》2006,32(9):1043-1058
This contribution focused on the solubility improvement of the poorly water-soluble steroid hormone progesterone which, in its natural state, presents a reduced oral bioavailability. In the first part of this study, two simple, reproducible methods that were candidates for use in the preparation of inclusion complexes with cyclodextrins were investigated. Solubility capacities of the progesterone complex with hydroxypropyl-β-CD (HPβ-CD), hydoxypropyl-γ-CD (HPγ-CD), permethyl-β-CD (PMβ-CD), and sulfobutylether-β-CD (SBEβ-CD), prepared by the freeze-drying and precipitation methods, were evaluated by Higuchi phase solubility studies. The results showed that HPβ-CD and PMβ-CD were the most efficient among the four cyclodextrins for the solubilization of progesterone, with the highest apparent stability constants. Therefore, dissolution studies were conducted on these latest progesterone/cyclodextrin complexes and physical mixtures. Two additional natural cyclodextrins, β-CD and γ-CD, were taken as references. Hence, the influence of more highly soluble derivatives of β-CD (HPβ-CD, PMβ-CD) on the progesterone dissolution rate, in comparison to pristine β-CD, alongside an increase in the cavity width for γ-CD versus β-CD, were investigated. The dissolution kinetics of progesterone dissolved from HPβ-CD, PMβ-CD, and γ-CD revealed higher constant rates in comparison to β-CD. Therefore, the aim of the second part of this study was to investigate the possibility of improving the dissolution rate of progesterone/β-CD binary systems upon formation of ternary complexes with the hydrophilic polymer, PEG 6000, as β-CD had the smallest progesterone solubility and dissolution capacity among the four cyclodextrins studied (β-CD, HPβ-CD, HPγ-CD and PMβ-CD). The results indicated that dissolution constant rates were considerably enhanced for the 5% and 10% progesterone/β-CD complexes in PEG 6000.
The interaction of progesterone with the cyclodextrins of interest on the form of the binary physical mixtures, complexes, or ternary complexes were investigated by differential scanning calorimetry (DSC) and Fourier transformed-infrared spectroscopy (FT-IR). The results proved that progesterone was diffused into the cyclodextrin cavity, replacing the water molecules and, in case of ternary systems, that the progesterone β-cyclodextrin was well dispersed into PEG, thus improving progesterone bioavailability for subsequent oral delivery in the same way as derivatized cyclodextrins. The present work proves that ternary complexes are promising systems for drug encapsulation. 相似文献
The interaction of progesterone with the cyclodextrins of interest on the form of the binary physical mixtures, complexes, or ternary complexes were investigated by differential scanning calorimetry (DSC) and Fourier transformed-infrared spectroscopy (FT-IR). The results proved that progesterone was diffused into the cyclodextrin cavity, replacing the water molecules and, in case of ternary systems, that the progesterone β-cyclodextrin was well dispersed into PEG, thus improving progesterone bioavailability for subsequent oral delivery in the same way as derivatized cyclodextrins. The present work proves that ternary complexes are promising systems for drug encapsulation. 相似文献
16.
Malika Perrier Alexis Deschamps Olivier Bouaziz Yves Brechet Frédéric Danoix Frédéric De Geuser Patricia Donnadieu Khalid Hoummada Philippe Maugis 《Metallurgical and Materials Transactions A》2012,43(13):4999-5008
In this article, we present a systematic study of precipitation kinetics in a Fe-Si-Ti alloy in the temperature range 723?K to 853?K (450?°C to 580?°C), combining complementary tools (transmission electron microscopy (TEM), atom probe tomography (APT), and small-angle neutron scattering (SANS)). We show that the Heusler phase Fe2SiTi dominates the precipitation process in the investigated time and temperature range, regardless of the details of the initial temperature history. A numerical model based on the evolution of precipitate size classes gives very good agreement with the experimental results, and its application to different alloy compositions provides directions for future alloy optimization. 相似文献
17.
18.
In this study, we synthesized a new hybrid material using well-Dawson K6[P2Mo18O62]·nH2O and a room temperature ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIM][BF4]). CHN elemental analysis showed that one mole of [P2Mo18O62]6− reacts with 6 moles of [BMIM]+ to form [BMIM]6P2Mo18O62. FT-IR spectra showed the presence of both 1-butyl-3-methylimidazolium cation and the Dawson anion. TG analysis displayed a relative thermal stability of the hybrid material compared to the parent Dawson POM. The new hybrid material [BMIM]6P2Mo18O62 was immobilized on glassy carbon (GC) electrode and the modified electrode was investigated by cyclic voltammetry and amperometry. Compared to the electrochemical behavior of dissolved [P2Mo18O62]6−, a slight shift in the redox peaks towards negative potentials is observed for the immobilized [BMIM]6P2Mo18O62. The relationship between the peak currents of the deposited [BMIM]6P2Mo18O62 film and scan rate is shown to be linear, which demonstrates a surface-confined electron transfer processes. [BMIM]6P2Mo18O62 modified electrode showed high sensitivities towards pH and shown to be active even at neutral pH. [BMIM]6P2Mo18O62 modified GC electrode was subjected to cyclic voltammetry and amperometry in the presence of ascorbic acid (AA) and found to exhibit a remarkable catalytic activity towards the oxidation of AA. The catalytic oxidation peak of AA at [BMIM]6P2Mo18O62 modified GC electrode occurs at low potential of ∼0 V vs Ag/AgCl at neutral pH and shifts to more positive potentials when pH decreases. Comparison between [BMIM]6P2Mo18O62 and [P2Mo18O62]6− modified GC films towards the oxidation of AA suggests that the significant decrease in the overpotentials recorded with [BMIM]6P2Mo18O62 film is related to the presence of ionic liquid cation in the hybrid material, which probably plays the role of the redox mediator. The resulting AA sensor [BMIM]6P2Mo18O62/GC has a significant sensitivity of ∼63 nA/μM AA, fast response time (<9 s), low detection limit (<0.1 μM), high selectivity towards endogenous interferences such as uric acid, acetaminophen and dopamine, a linear range from 0.1 μM to at least 22 mM AA and was stable for at least 2 weeks. In addition, such AA sensors can operate in a pH range from 0 to at least 7. 相似文献
19.
Sylvain Meille Malika Sadaoui Pascal Reynaud Gilbert Fantozzi 《Journal of the European Ceramic Society》2003,23(16):3105-3112
Controlled crack propagation tests were performed on single edge notched bend samples to investigate the crack growth behaviour of dry plaster. The influence of the relative notch depth on the crack resistance curve has been studied and appears to be very important. The results are discussed considering a qualitative model based on the specific microstructure of plaster and in situ observations of the crack propagation. Two mechanisms acting at different scales and undergoing complex interactions are involved: crack bridging by small gypsum crystals acting locally behind the crack tip and secondary cracking in a macroscopic frontal process zone. Interaction of the main crack with secondary ones undergoes substantial branching and crack accelerations leading to bridging destruction due to sudden crack opening. 相似文献
20.
Anne‐Lise Bottalla Malika Ibrahim‐Ouali Maurice Santelli Roland Furstoss Alain Archelas 《Advanced Synthesis \u0026amp; Catalysis》2007,349(7):1102-1110
Two microbial epoxide hydrolases – i.e., Aspergillus niger (AnEH) and Rhodococcus erythropolis (the so‐called “Limonene EH”: LEH) were used to achieve, for the first time, the biocatalysed hydrolytic kinetic resolution (BHKR) of spiroepoxide rac‐ 1 . This compound is a strategic key building block allowing the synthesis of 11‐heterosteroids. Interestingly enough, the two enzymes exhibited opposite and therefore complementary enantioselectivity allowing us to isolate the residual (R,R)‐ 1 (from AnEH) and the residual (S,S)‐ 1 (from LEH) in nearly enantiopure forms (>98 %). Their absolute configurations were determined by X‐ray crystallography. An opposite regioselectivity of the oxirane ring opening for both enantiomers of substrate 1 , determined using H218O labelling and chiral GC‐MS analysis, was also observed, corresponding to an attack at the less substituted carbon atom using AnEH, and at the most substituted carbon atom using LEH. A chemical process‐improving methodology was also developed. This allowed us to obtain both enantiomers of the substrate in high enantiomeric purity (99 %) and optimised quantity. In the case of the AnEH, the use of a biphasic (water/isooctane) reaction medium allowed us to increase the global substrate concentration up to 200 g/ L. The preparation of both enantiomers of 1 clearly paves the way to the preparative scale synthesis and biochemical evaluation of the corresponding 11‐heterosteroid enantiomers. 相似文献