3,131 research outputs found
Dry oil powders and oil foams stabilised by fluorinated clay platelet particles
A series of platelet sericite particles coated to different extents with a fluorinating agent has been characterised and their behaviour in mixtures with air and oil studied. The material which forms by vigorous shaking depends on both the surface tension of the oil and the surface energy of the particles which control their degree of wetting. Oil dispersions are formed in liquids of relatively low tension (<22 mN m−1), e.g. hexane and cyclomethicone, for all particles. Particle-stabilised air-in-oil foams form in liquids of higher tension, e.g. dodecane and phenyl silicone, where the advancing three-phase contact angle θ, measured on a planar substrate composed of the particles into the liquid, lies between ca. 65° and 120°. For oils of tension above 27 mN m−1 like squalane and liquid paraffin with particles for which θ > 70°, we have discovered that dry oil powders in which oil drops stabilised by particles dispersed in air (oil-in-air) can be prepared by gentle mixing up to a critical oil : particle ratio (COPR) and do not leak oil. These powders, containing up to 80 wt% oil, release the encapsulated oil when sheared on a substrate. For many of the systems forming oil powders, stable liquid oil marbles can also be prepared. Above the COPR, catastrophic phase inversion occurs yielding an ultra-stable air-in-oil foam. We thus demonstrate the ability to disperse oil drops or air bubbles coated with particles within novel materials
Sonolytic Oxidation of Tc(IV)O2nH2O Nanoparticles to Tc(VII)O4 in Aqueous Solution
Sonolysis of a hydrosol of TcO2nH2O was investigated in the Ar- or He- atmosphere. Colloidal TcO2nH2O nanoparticles were irradiated with a 200 kHz and 1.25 W/cm2 ultrasound. It was found that the TcO2nH2O colloids dispersed in an aqueous solution (under Ar or He atmosphere) was completely dissolved by ultrasonic irradiation (200 kHz, 200 W). The original brownish black color of the suspension slowly disappeared leaving behind a colorless solution. This change suggests that oxidation of Tc(IV) to Tc(VII) takes place. The oxidation was almost complete during 30 minutes sonication time under argon atmosphere for initial concentration of 6.0E-5 M. Addition of t-butyl alcohol, an effective radical scavenger which readily reacts with OH radicals, supressed the dissolution of TcO2nH2O colloids. This reaction indicates that TcO2nH2O molecules are oxidized by OH radicals produced in cavitation bubbles. Received: 20 November 2009; Revised:14 April 2010; Accepted: 18 April 201
Sonolytic Oxidation of Tc(IV)O2nH2O Nanoparticles to Tc(VII)O4 in Aqueous Solution
Sonolysis of a hydrosol of TcO2nH2O was investigated in the Ar- or He- atmosphere. Colloidal TcO2nH2O nanoparticles were irradiated with a 200 kHz and 1.25 W/cm2 ultrasound. It was found that the TcO2nH2O colloids dispersed in an aqueous solution (under Ar or He atmosphere) was completely dissolved by ultrasonic irradiation (200 kHz, 200 W). The original brownish black color of the suspension slowly disappeared leaving behind a colorless solution. This change suggests that oxidation of Tc(IV) to Tc(VII) takes place. The oxidation was almost complete during 30 minutes sonication time under argon atmosphere for initial concentration of 6.0E-5 M. Addition of t-butyl alcohol, an effective radical scavenger which readily reacts with OH radicals, supressed the dissolution of TcO2nH2O colloids. This reaction indicates that TcO2nH2O molecules are oxidized by OH radicals produced in cavitation bubbles. Received: 20 November 2009; Revised:14 April 2010; Accepted: 18 April 201
Hot Atom Chemistry and Recoil Implantation Induced Reaction in Geometrical Isomers of Tris-(benzoylacetonato)Cr(III)
開始ページ、終了ページ: 冊子体のページ付
Charge-Density-Wave Ordering in the Metal-Insulator Transition Compound PrRu4P12
X-ray and electron diffraction measurements on the metal-insulator (M-I)
transition compound PrRuP have revealed the emergence of a periodic
ordering of charge density around the Pr atoms. It is found that the ordering
is associated with the onset of a low temperature insulator phase. These
conclusions are supported by the facts that the space group of the crystal
structure transforms from Im to Pm below the M-I transition
temperature and also that the temperature dependence of the superlattice peaks
in the insulator phase follows the squared BCS function. The M-I transition
could be originated from the perfect nesting of the Fermi surface and/or the
instability of the electrons.Comment: 4 pages, 5 figures, Phys. Rev. B (2004) (in press
- …