Synthesis and characterization of monodisperse spherical zirconia particles; ; Pirard, René et alin Journal of Sol-Gel Science and Technology (1997), 8 Detailed reference viewed: 21 (3 ULg) Synthesis and characterization of nanostructured mesoporous zirconia catalyst supports using non-ionic surfactants as templating agents; ; Léonard, Alexandre et alin Studies in Surface Science and Catalysis (2002), 143 The formation of nanostructured porous zirconia catalyst supports using non-ionic surfactants as templating agents has been studied in order to optimize the synthesis conditions without addition of ... [more ▼] The formation of nanostructured porous zirconia catalyst supports using non-ionic surfactants as templating agents has been studied in order to optimize the synthesis conditions without addition of structure stabilizing agents such as sulfate or phosphate anions. The effect of the quantity of added zirconium source with respect to the surfactant concentration in solution has been studied. We also examined the role played by the surfactant during the synthesis. Further investigations have shown that the pore diameters could be increased towards the mesoporous domain if heating time and temperature are raised. The present work reveals that the control of the balance between the precipitation rate of zirconia and the interaction of zirconium source will be fatal in the formation of nanostructured porous zirconia. [less ▲] Detailed reference viewed: 8 (1 ULg) Synthesis and characterization of new inorganic polymeric composites based on kaolin or white clay and on ground-granulated blast furnace slag; Liégeois, Monique ; Rulmont, André et alin Journal of Materials Research (2003), 18(11), 2571-2579 Alkali activation of dehydroxylated kaolin or clay yielded high-strength polymeric materials, so-called geopolymers. They were synthesized by mixing the aluminosilicate with solutions of sodium ... [more ▼] Alkali activation of dehydroxylated kaolin or clay yielded high-strength polymeric materials, so-called geopolymers. They were synthesized by mixing the aluminosilicate with solutions of sodium metasilicate and KOH followed by adding 45 wt.% of ground-granulated blast furnace slag. The influence of the aluminosilicate source, its activation temperature, and the order of mixing raw materials were studied on the workability of the blending paste, the microstructure, and the Vickers hardness of the geopolymer samples. The polymeric material is completely amorphous according to x-ray diffraction. Solid-state 27Al and 29Si magic-angle-spinning nuclear magnetic resonance showed that the geopolymer consists of AlO 4 and SiO 4 tetrahedra linked together through a polymeric network constituted by branched entities SiQ 4(4Al) and SiQ 4(3Al), but also by less-polymerized silicates SiQ 1 and SiQ 2. Scanning electron microscopy showed a homogeneous polymeric gel matrix containing unreacted slag (and quartz) grains; thermogravimetric analysis and differential scanning calorimetry exhibited a high content of water and an elevated melting point (1260 °C). Vickers hardness values are in the range of 200 MPa. [less ▲] Detailed reference viewed: 3 (0 ULg) Synthesis and characterization of non-covalent liquid crystalline diblock copolymers; ; Sobry, Roger et alin Macromolecular Chemistry and Physics (2000), 201(1), 31-41 Poly(dimethylaminoethylmethacrylate)-b-poly(sodium methacrylate) diblocks, (polyDMAEMA-b-polyMA), were synthesized as precursors of liquid crystalline (LC) copolymers. These LC copolymers were prepared by ... [more ▼] Poly(dimethylaminoethylmethacrylate)-b-poly(sodium methacrylate) diblocks, (polyDMAEMA-b-polyMA), were synthesized as precursors of liquid crystalline (LC) copolymers. These LC copolymers were prepared by pro-ton-transfer between a carboxylic acid-containing meso-gen (A) and the dimethylamino substituent of the poly-DMAEMA block and by electrostatic interactions between the polyMA subunits and an ammonium-contain-ing mesogen (B). When mesogen A is complexed with DMAEMA units, a dramatic enhancement of the meso-phase stability is noted. The mesogenic properties of these LC copolymers were compared to those ones of the parent LC homopolymers, in relation to the copolymer composi-tion. The supramolecular organization of the LC diblock copolymers was studied by small-angle X-ray scattering (SAXS), and smectic mesophases were observed in some LC (co)polymers. For samples containing a major LC block, a smectic mesophase coexists with microphases formed by the second amorphous block. Different organizations, including a body-centered lattice of spheres and a hexagonal array of cylinders, were observed, depending on the investigated copolymers and their composition. When the LC block is the minor component, it forms microdomains too small for a liquid crystalline order to emerge. Moreover, no supramolecular organization of these dispersed microdomains was detected by SAXS. A homogeneous smectic mesophase was observed when the two blocks are bearing liquid crystalline moieties. [less ▲] Detailed reference viewed: 17 (2 ULg) Synthesis and characterization of novel vinyl copolymers containing N-vinylphthalimide: Comonomers reactivity ratios and thermal stability; ; Jérôme, Robert ![]() in European Polymer Journal (2007), 43(9), 3849-3855 N-Vinylphthalimide (NVPh) was copolymerized with p-methylstyrene (PMS), p-methoxystyrene (PMOS) and p-chlorostyrene (PCIS) at 60 degrees C, with 2,2'-azo-bis-isobutyronitrile as an initiator. Copolymer ... [more ▼] N-Vinylphthalimide (NVPh) was copolymerized with p-methylstyrene (PMS), p-methoxystyrene (PMOS) and p-chlorostyrene (PCIS) at 60 degrees C, with 2,2'-azo-bis-isobutyronitrile as an initiator. Copolymer composition was determined by elemental analysis in case of the N-vinylphthalimide and p-methylstyrene comonomer pair, whereas proton nuclear magnetic resonance was used for the analysis of the two other copolymers. The reactivity ratios for each comonomer pair were estimated by the classical Fineman-Ross and Kelen-Tudos linear techniques. These data showed that N-vinylphthalimide was less reactive in all the cases and that the comonomer distribution, that was basically random in the poly(N-vinylphthalimide-co-p-methylstyrene) and poly(N-vinylphthalimide-co-p-chlorostyrene) copolymers, was rather alternate in the third poly(N-vinylphthalimide-co-p-methoxystyrene) copolymer. The difference observed in the reactivity ratios was discussed in reference to the structure of the comonomer units and the parent radicals. The thermal properties of the copolymers and model homopolymers were investigated by differential scanning calorimetry and thermogravimetric analysis. [less ▲] Detailed reference viewed: 35 (2 ULg) Synthesis and characterization of poly(methyl methacrylate)-block-poly(n-butyl acrylate)-block-poly(methyl methacrylate) copolymers by two-step controlled radical polymerization (ATRP) catalyzed by NiBr2(PPh3)2, 1+; ; et al in Macromolecules (1999), 32(25), 8277-8282 Poly(methyl methacrylate)-block-poly(n-butyl acrylate)-block-poly(methyl methacrylate) triblock copolymers (MnBM) have been synthesized by the sequential controlled radical polymerization (atom transfer ... [more ▼] Poly(methyl methacrylate)-block-poly(n-butyl acrylate)-block-poly(methyl methacrylate) triblock copolymers (MnBM) have been synthesized by the sequential controlled radical polymerization (atom transfer radical polymerization, ATRP) of n-butyl acrylate (n-BuA) followed by methyl methacrylate (MMA). The polymerization of n-BuA has been first initiated by the difunctional (diethyl meso-2,5-dibromoadipate) initiator in the presence of the NiBr2(PPh3)2 catalyst. After isolation, the α,ω-dibromo poly(n-butyl acrylate) chains have been used as macroinitiators for the polymerization of either n-BuA or MMA leading to chain extension or to the desired triblock copolymers, respectively. The kinetic study of the two-step process has shown that the initiation of the MMA polymerization by the poly(n-BuA) macroinitiator is slow and leads to PMMA outer blocks of broad polydispersity. Differential scanning calorimetry (DSC) and dynamical mechanical analysis (DMA) have confirmed the two-phase morphology of the triblocks. Finally, DMA and tensile testing of these copolymers have emphasized poor mechanical properties in possible relation to the broad polydispersity of the PMMA outer blocks. [less ▲] Detailed reference viewed: 47 (3 ULg) Synthesis and characterization of porous carbon xerogels and ordered mesoporous carbons for anode materials in Li-based batteriesLéonard, Alexandre ; Pirard, Jean-Paul ; Job, Nathalie ![]() in Fagadar-Cosma, Eugenia (Ed.) Insights into novel solid materials, their recyclability and integration into Li polymer batteries for EVs. Future research directions in this field.:Book of abstracts (2012, July 04) Detailed reference viewed: 7 (2 ULg) Synthesis and characterization of porous silica-alumina xerogels; ; et al Conference (1995) Detailed reference viewed: 11 (2 ULg) Synthesis and characterization of porous silica-alumina xerogels; ; et al in Journal of Sol-Gel Science and Technology (1997), 8 Detailed reference viewed: 8 (3 ULg) Synthesis and characterization of random copolyesters of epsilon-caprolactone and 2-oxepane-1,5-dione; Lecomte, Philippe ; Dubois, Philippe et alin Macromolecules (2003), 36(8), 2609-2615 2-Oxepane-1,5-dione (OPD) has been synthesized by the Baeyer-Villiger oxidation of 1,4-cyclohexanedione and copolymerized with epsilon-caprolactone. This random copolymerization has been initiated by ... [more ▼] 2-Oxepane-1,5-dione (OPD) has been synthesized by the Baeyer-Villiger oxidation of 1,4-cyclohexanedione and copolymerized with epsilon-caprolactone. This random copolymerization has been initiated by different metal derivatives, i.e., tin octanoate, dibutyltin dimethoxide, and aluminum isopropoxide. Dibutyltin dimethoxide is the preferred initiator, and the course of polymerization is controlled by the competition of the ketone of OPD and the ester of the lactones for coordination to the initiator. Semicrystalline copolymers are formed, whose the randomness has been confirmed by DSC, H-1 NMR, and C-13 NMR analysis. A single melting temperature (Tm) has been observed, which varies regularly and monotonically with the OPD content as result of a cocrystallization phenomenom. The single glass transition temperature (Tg) obeys the Fox equation. [less ▲] Detailed reference viewed: 39 (4 ULg) Synthesis and characterization of recyclable chemically cross-linked shape memory materialsDefize, Thomas ; Riva, Raphaël ; Thomassin, Jean-Michel et alConference (2012, September 10) Detailed reference viewed: 10 (4 ULg) Synthesis and characterization of recyclable chemically-crosslinked shape memory materialsDefize, Thomas ; Riva, Raphaël ; Lecomte, Philippe et alPoster (2011, May 12) Detailed reference viewed: 16 (4 ULg) Synthesis and characterization of reversibly core cross-linked micelles sensitive to reductive environmentCajot, Sébastien ; ; et alPoster (2011, May 12) Detailed reference viewed: 30 (13 ULg) Synthesis and characterization of reversibly cross-linked shape memory materialsDefize, Thomas ; Riva, Raphaël ; Thomassin, Jean-Michel et alPoster (2011, April 29) Detailed reference viewed: 3 (1 ULg) Synthesis and characterization of reversibly cross-linked shape memory materialsDefize, Thomas ; Riva, Raphaël ; Lecomte, Philippe et alPoster (2010, September 07) Detailed reference viewed: 17 (3 ULg) Synthesis and characterization of reversibly cross-linked shape memory materialsDefize, Thomas ; Riva, Raphaël ; Thomassin, Jean-Michel et alPoster (2010, November 29) Detailed reference viewed: 15 (3 ULg) Synthesis and compatibilization ability of hydrogenated polybutadiene-b-polyamide 6 diblock copolymer in low density polyethylene and polyamide 6 blends; ; Jérôme, Robert ![]() in Polymer (2002), 43(19), 5347-5354 This paper describes the synthesis of hydrogenated polybutadiene-b-polyamide 6 (HPB-b-PA6), a pure diblock copolymer, which consists of three main steps: synthesis of hydroxyl terminated polybutadiene ... [more ▼] This paper describes the synthesis of hydrogenated polybutadiene-b-polyamide 6 (HPB-b-PA6), a pure diblock copolymer, which consists of three main steps: synthesis of hydroxyl terminated polybutadiene, its hydrogenation and functionalization with an epsilon-caprolactam blocked diisocyanate. In a third step the functionalized HPB is copolymerized with epsilon-caprolactam monomer via ring opening anionic polymerization. The compatibilization ability of the synthesized pure diblock copolymer was evaluated in low-density polyethylene (LDPE)/polyamide 6 (PA6) blends. The investigation includes phase morphology development using both optical and electron scanning microscopy. The ultimate tensile properties of the modified and non-modified blends were also evaluated. The synthesized pure diblock copolymer exhibits very interesting interfacial activity both in terms of particle size reduction and improvement of the interfacial adhesion between the incompatible LDPE/PA6 phases. The tensile properties of the investigated blends were also significantly affected by the addition of the copolymer. The efficiency of compatibilization was found to be very sensitive to the molecular characteristics such as composition and molecular weight of the copolymer. Among the copolymers investigated a copolymer containing 24 wt% PA6 and having a total molecular weight (M) over bar (a) of 87,000 was found to exhibit the most efficient interfacial activity. [less ▲] Detailed reference viewed: 16 (0 ULg) Synthesis and complete processing of a high-molecular-weight precursor polypeptide to viral structural proteins in toad oocytes micro-injected with avian myeloblastosis virus ribonucleic acid.; ; et al in Biochemical Society Transactions (1977), 5 Detailed reference viewed: 8 (6 ULg) Synthesis and deposition of water-dispersed prussian blue nanocrystals on polymers and CNTs; ; et al in Progress in Colloid & Polymer Science (2006), 132 Nanoparticles can be used for decoration and functionalization of single polymer molecules that have been adsorbed to a solid substrate. Initial attempts to prepare Prussian Blue nanoclusters by a layer ... [more ▼] Nanoparticles can be used for decoration and functionalization of single polymer molecules that have been adsorbed to a solid substrate. Initial attempts to prepare Prussian Blue nanoclusters by a layer-by-layer deposition technique of hexacyanoferrate anions and ferric cations onto isolated polycation chains in water failed because of the desorption of the first layer upon deposition of the next one. A simple method for the preparation of charge-stabilized Prussian Blue nanoparticles of readily adjustable size is reported. Prussian Blue nanoparticles have been purified by addition of non-solvents and redispersed in water without aggregation. Thus formed Prussian Blue nanoparticles are crystalline and display a long-range ferromagnetic ordering at 5.1 K. Prussian Blue nanoparticles were selectively deposited along single polycation molecules to form a one-dimensional array or were attached to the surface of carbon nanotubes (CNTs) functionalized with poly2-vinylpyridine (P2VP). These nanoparticle-based nanostructures might be useful materials for manufacture of electrooptical devices, or mechanically robust ion-sieving membranes. [less ▲] Detailed reference viewed: 20 (1 ULg) Synthesis and design of potential ATP-sensitive potassium channel openers bearing some structural features of benzopyrans (bioisosteres) and benzo(pyrido)thiadiazinedioxides; Pirotte, Bernard ; et alPoster (1996, September) Detailed reference viewed: 1 (0 ULg) |
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