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Titania thermal analysis

Polydimethylsiloxane and Zr oxo species have been reacted to give hybrid materials which were characterized by solid-state NMR.149 TEOS/PEG (polyethylene glycol) materials are biphasic systems. The materials were studied by 13C NMR, EPR, and thermal analysis.150 Other systems studied include titania/polyvinylacetate,151 titania/PEG,152 silica/polyacrylates,153 polyimide/ silica,154"156 linseed oil alkyds/titania,157 and PVC/titania and vanadia/sulfonated polyaniline... [Pg.720]

The sol-gel titania-silica mixed oxide contained 20 wt% titania. The catalyst was synthesized imder acidic conditions [5]. The acidic hydrolysant was added to an isopropanohc solution of tetraisopropoxytitanitam(IV) modified by acetylacetone (molar ratio alkoxide acetylacetone =1 1) and tetramethoxysilicon(IV). The water alkoxide acid molar ratio was 5 1 0.09. The resulting gel was dried by semicontinuous extraction with supercritical COg at 40 °C and 240 bar, and stored in a closed vessel under Ar. After calcination in flowing air at 600 °C, the BET smface area was 648 m g and the specific pore volume 2.9 cm g". Details on the synthesis and characterization of the sol-gel titania-sihca by means of FTIR, Raman and UV-vis spectroscopies, Ng-physisorption, XRD, XPS, TEM and thermal analysis have been reported previously [5, 6, 14, 15]. [Pg.330]

In view of this, nano titanium dioxide was synthesized and prepared as suspension with PVP solution. The mixture was set to electro-spin into fibre at 18KV. The e-spun fibre was subjected to differential thermal analysis to obtain the sintering profile for the titania fibre. The titania fibre was sintered at 500°C and 1200°C. The sintered phases and microstructural of titania fibre were analysed by using X-ray diffractometer and scanning electron microscope and presented. The cross-linked titania fibre formed a web-like structure maybe reduced the nano risk as compared to the nanoparticles. [Pg.357]

In this framework, in the specially designed mortars consisting of binders of either lime and metakaolin or natural hydraulic lime and fine aggregates of carbonate nature, nano-titania of anatase (90 per cent) and rutile (10 per cent) form has been added (4.5-6% w/w of binder). The aim was to study the effect of nano-titania in the hydration and carbonation of the above binders and to compare the physico-chemical properties of the nano-titania mortars with those mortars without nano-titania, used as reference. Thermal analysis (DTA-TG), infrared spectroscopy (FTIR), X-ray diffraction (XRD) and scanning electron microscopy (SEM) analyses were performed to investigate the evolution of carbonation, hydration and hydraulic compound formation during a six-month curing period. Furthermore, the stone-mortar interfaces, the adhesion resistance to external mechanical stress, relative to the physicochemical characteristics of the stone-mortar system and the role of the nano-titania as additive, were reported and are discussed in this chapter. [Pg.81]

Figure 3. Differential thermal analysis of ahimina-titania supports. Air atmosphere, lO C/min. Samples a) AT05 b) ATIO c) AT40. Figure 3. Differential thermal analysis of ahimina-titania supports. Air atmosphere, lO C/min. Samples a) AT05 b) ATIO c) AT40.
Nishide, T., T. Tanaka, T. Yabe (2004) Temperature programmed desorption analysis of sol-gel-derived titania films. Journal of thermal analysis and calorimetry. 90,373-378. [Pg.346]

TOA. See Thermogravimetric analysis Theory of deformation, 437-448 Thermal analysis, 16, 549, 570, 604, 711 Thermal conductivity, 760 Thermal decomposition, 272 Thermal expansion, 506, 550, 551, 554, 702, 737, 748-751, 760, 766-767 titania silica xerogels, 295, 597, 598, 776 Thermal stress, 436, 494 Thermodynamic activity, 474 Thermodynamic barrier, 732-735, 752-753 Thermodynamics, sols, gels, glasses,... [Pg.461]

The structures of the gold catalysts were observed using a Hitachi H-9000 electron microscope operated at 300 kV. X-ray diffraction (XRD) analysis was made by using a Rad-B system (Rigaku Denki Co.Ltd.). Infrared spectra were taken with a Nicolet 20-SXC spectrometer. For the IR analysis, each sample was mixed with KBr( 2wt.% for magnesia 10 wt.% for titania), and pressed into a thin wafer. Differential thermal analysis (DTA) was made by using a SSC-5200 thermal analyzer (Seiko Denshi Kogyo Co.Ltd.). X-ray photoelectron spectroscopy (XPS) was measured with a SSX-100 spectrometer (Surface Science Laboratories, Inc.). [Pg.696]

Data showing dehydrogenation onset temperature as determined by thermal gravitational analysis (TGA) and oxide surface area for MgH2 milled for 20 h with 20 wt% of various oxides (Croston, 2007). Nomenclature of y-axis labels refers to the wt% ratio of oxides followed by the calcination temperature of the oxide particle in °C. The Ti-5Pd and Ti-IPd refer to 5 and 1 wt% Pd distributed on the 20 wt% titania. Unmarked row represents milled MgH2 with no additive. [Pg.371]


See other pages where Titania thermal analysis is mentioned: [Pg.45]    [Pg.145]    [Pg.13]    [Pg.203]    [Pg.339]    [Pg.75]    [Pg.76]    [Pg.79]    [Pg.150]    [Pg.316]    [Pg.328]    [Pg.85]    [Pg.328]    [Pg.54]    [Pg.200]    [Pg.250]    [Pg.117]    [Pg.1177]    [Pg.100]    [Pg.250]   
See also in sourсe #XX -- [ Pg.408 ]




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