Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Nanoparticles cationic

Figure 6. TEM images obtained at an accelerating voltage of 200 kV of Pt-core/Ru-shell nanoparticles prepared by sequential soni-cation of 1 mM Pt(ll) and 1 mM Ru(lll) ions at 213 kHz. Two representative particles are shown at different magnification. (Reprinted from Ref [141], 2006, with permission from American Chemical Society.)... Figure 6. TEM images obtained at an accelerating voltage of 200 kV of Pt-core/Ru-shell nanoparticles prepared by sequential soni-cation of 1 mM Pt(ll) and 1 mM Ru(lll) ions at 213 kHz. Two representative particles are shown at different magnification. (Reprinted from Ref [141], 2006, with permission from American Chemical Society.)...
When the metal nanoparticles are inserted into zeolite supercages, the size of the metal particles is confined according to the size of the supercage. However, after reduction of the precursor metal ions in a stream of hydrogen, the protons replacing the metal ions in the cation exchange position also interfere with the metal particles, influencing thereby their chemisorption and catalytic properties. [Pg.90]

In 1994, thiols were firstly used as stabilizers of gold nanoparticles [6a]. Thiols form monolayer on gold surface [18] and highly stable nanoparticles could be obtained. Purification of nanoparticles can be carried out, which makes chemical method of metal nanoparticles a real process for nanomaterial preparation. Various thiol derivatives have been used to functionalize metal nanoparticles [6b, 19]. Cationic and anionic thiol compounds were used to obtain hydrosols of metal nanoparticles. Quaternary ammonium-thiol compounds make the nanoparticle surface highly positively charged [20]. In such cases, cationic nanoparticles were densely adsorbed onto oppositely charged surfaces. DNA or other biomolecule-attached gold nanoparticles have been proposed for biosensors [21]. [Pg.454]

NMR measurements are very useful to understand the properties of the stabilizing reagents of metal nanoparticles. Author s group reported the structure of stabilization of non-ionic and cationic surfactants on platinum nanoparticles [22] and that of ternary amines on rhodium nanoparticles [23]. Such information is considerably important for applications of nanoparticles such as... [Pg.455]

Some of the reports are as follows. Mizukoshi et al. [31] reported ultrasound assisted reduction processes of Pt(IV) ions in the presence of anionic, cationic and non-ionic surfactant. They found that radicals formed from the reaction of the surfactants with primary radicals sonolysis of water and direct thermal decomposition of surfactants during collapsing of cavities contribute to reduction of metal ions. Fujimoto et al. [32] reported metal and alloy nanoparticles of Au, Pd and ft, and Mn02 prepared by reduction method in presence of surfactant and sonication environment. They found that surfactant shows stabilization of metal particles and has impact on narrow particle size distribution during sonication process. Abbas et al. [33] carried out the effects of different operational parameters in sodium chloride sonocrystallisation, namely temperature, ultrasonic power and concentration sodium. They found that the sonocrystallization is effective method for preparation of small NaCl crystals for pharmaceutical aerosol preparation. The crystal growth then occurs in supersaturated solution. Mersmann et al. (2001) [21] and Guo et al. [34] reported that the relative supersaturation in reactive crystallization is decisive for the crystal size and depends on the following factors. [Pg.176]

The objective of this monograph is to include all major studies of metal ions in their aqueous solutions as well as some other important studies in their zerovalent metallic state or in alloys, since the nanoparticles of many of these metals have become too important. Besides, the study of the precipitation of metal ions in aqueous solutions, upon sonication, which has been carried out in our laboratory, would also be discussed. Some of such data include unpublished work. The sequence of metallic ions in this chapter are as they come in the sequence of wet chemical analysis of basic radicals, besides the cationic charge has been kept in mind to make groups and sequences that follow the detailed description. [Pg.221]

The production of CLS by the melt dispersion technique is based on the melting of the lipid core material together with the lipophilic agent (i.e., phospholipids). Afterward, a warm aqueous solution is added to the molten material and is mixed by various methods (i.e., mechanical stirring, shaking, sonication, homogenization). Then the preparation is rapidly cooled until lipid solidification and the formation of particle dispersion. This method was used by Olbrich et al. [19] to produce the cationic solid lipid nanoparticles to use as novel transfection agent. [Pg.5]


See other pages where Nanoparticles cationic is mentioned: [Pg.352]    [Pg.492]    [Pg.648]    [Pg.352]    [Pg.492]    [Pg.648]    [Pg.79]    [Pg.84]    [Pg.84]    [Pg.84]    [Pg.95]    [Pg.97]    [Pg.435]    [Pg.508]    [Pg.179]    [Pg.52]    [Pg.67]    [Pg.102]    [Pg.294]    [Pg.310]    [Pg.335]    [Pg.367]    [Pg.455]    [Pg.233]    [Pg.234]    [Pg.165]    [Pg.168]    [Pg.176]    [Pg.244]    [Pg.257]    [Pg.119]    [Pg.121]    [Pg.242]    [Pg.238]    [Pg.21]    [Pg.161]    [Pg.161]    [Pg.162]    [Pg.173]    [Pg.182]    [Pg.255]    [Pg.259]    [Pg.456]    [Pg.89]    [Pg.262]    [Pg.2]    [Pg.14]   
See also in sourсe #XX -- [ Pg.15 ]




SEARCH



Cationic Shell Crosslinked Kendel-like Nanoparticles

Nanoparticle cationic

© 2024 chempedia.info