02718nas a2200229 4500008004100000022001400041245012700055210006900182260007100251300001600322490000700338520184800345100002002193700001902213700002202232700001502254700002002269700002502289700003002314700001502344856012902359 2005 eng d a0743-746300aCobalt and magnesium ferrite nanoparticles: preparation using liquid foams as templates and their magnetic characteristics0 aCobalt and magnesium ferrite nanoparticles preparation using liq a1155 16TH ST, NW, WASHINGTON, DC 20036 USAbAMER CHEMICAL SOCcNOV a10638-106430 v213 a

An easy and convenient method for the synthesis of cobalt and magnesium ferrite nanoparticles is demonstrated using liquid foams as templates. The foam is formed from an aqueous mixture of an anionic surfactant and the desired metal ions, where the metal ions are electrostatically entrapped by the surfactant at the thin borders between the foam bubbles and their junctions. The hydrolysis is carried out using alkali resulting in the formation of desired nanoparticles, with the foam playing the role of a template. However, in the formation of ferrites with the formula MFe2O4, where the metal ion and iron possess oxidation states of +2 and +3, respectively, forming a foam from a 1:2 mixture of the desired ionic solutions would lead to a foam composition at variance with the original solution mixture because of greater electrostatic binding of ions possessing a greater charge with the surfactant. In our procedure, we circumvent this problem by preparing the foam from a 1:2 mixture of M2+ and Fe2+ ions and then utilizing the in situ conversion of Fe2+ to Fe3+ under basic conditions inside the foam matrix to get the desired composition of the metal ions with the required oxidation states. The fact that we could prepare both CoFe2O4 and MgFe2O4 particles shows the vast scope of this method for making even multicomponent oxides. The magnetic nanoparticles thus obtained exhibit a good crystalline nature and are characterized by superparamagnetic properties. The magnetic features observed for CoFe2O4 and MgFe2O4 nanoparticles are well in accordance with the expected behaviors, with CoFe2O4 particles showing higher blocking temperatures and larger coercivities. These features can easily be explained by the contribution of Co2+ sites to the magnetocrystalline anisotropy and the absence of the same from the Mg2+ ions.

1 aBala, Tanushree1 aSankar, C., R.1 aBaidakova, Marina1 aOsipov, V.1 aEnoki, Toshiaki1 aJoy, Pattayil, Alias1 aPrasad, Bhagavatula L. V.1 aSastry, M. uhttps://library.ncl.res.in/content/cobalt-and-magnesium-ferrite-nanoparticles-preparation-using-liquid-foams-templates-and-001499nas a2200169 4500008004100000245008500041210006900126260000800195300001400203490000600217520083500223653008401058100002001142700002001162700003001182856011701212 2007 eng d00aFerromagnetic resonance in nanomagnetic metal core and noble metal shell systems0 aFerromagnetic resonance in nanomagnetic metal core and noble met cSEP a3134-31390 v93 a

The change in the line widths in the ferromagnetic resonance (FMR) spectra of Co and Ni nanoparticles upon shell formation with noble metals like gold or silver are described. The NicoreAgshell, CocoreAgshell, and CocoreAushell nanoparticles were prepared by a simple transmetallation reaction between the Co and Ni nanoparticles and the Ag+ or AuCl−4 ions. It is revealed that the FMR line width decreases upon Ag shell formation whereas it increases upon core–shell composite formation with Au. Several probable explanations such as the differences in size distributions before and after the reaction or the changes occurring in shape anisotropy of the particles due to the shell formation or the different extents of electronic interaction between the core and shell materials have been offered for this observation.

10aFmr Study; Line Width Comparison; Magnetic Core-Noble Metal Shell Nanoparticles1 aBala, Tanushree1 aEnoki, Toshiaki1 aPrasad, Bhagavatula L. V. uhttps://library.ncl.res.in/content/ferromagnetic-resonance-nanomagnetic-metal-core-and-noble-metal-shell-systems02037nas a2200253 4500008004100000022001400041245011800055210006900173260007100242300001400313490000700327520109000334100002101424700002301445700002201468700001801490700002301508700002001531700003001551700002401581700002901605700001901634856013001653 2008 eng d a0743-746300aBacteria-mediated precursor-dependent biosynthesis of superparamagnetic iron oxide and iron sulfide nanoparticles0 aBacteriamediated precursordependent biosynthesis of superparamag a1155 16TH ST, NW, WASHINGTON, DC 20036 USAbAMER CHEMICAL SOCcJUN a5787-57940 v243 a

The bacterium Actinobacter sp. has been shown to be capable of extracellularly synthesizing iron based magnetic nanoparticles, namely maghemite (gamma-Fe2O3) and greigite (Fe3S4) Under ambient conditions depending on the nature of precursors used. More precisely, the bacterium synthesized maghemite when reacted with ferric chloride and iron sulfide when exposed to the aqueous solution of ferric chloride-ferrous sulfate. Challenging the bacterium with different metal ions resulted in induction of different proteins, which bring about the specific biochemical transformations in each case leading to the observed products. Maghemite and iron sulfide nanoparticles show superparamagnetic characteristics as expected. Compared to the earlier reports of magnetite and greigite synthesis by magnetotactic bacteria and iron reducing bacteria, which take place strictly under anaerobic conditions, the present procedure offers significant advancement since the reaction occurs under aerobic condition. Moreover, reaction end products can be tuned by the choice of precursors used.

1 aBharde, Atul, A.1 aParikh, Rasesh, Y.1 aBaidakova, Marina1 aJouen, Samuel1 aHannoyer, Beatrice1 aEnoki, Toshiaki1 aPrasad, Bhagavatula L. V.1 aShouche, Yogesh, S.1 aOgale, Satishchandra, B.1 aSastry, Murali uhttps://library.ncl.res.in/content/bacteria-mediated-precursor-dependent-biosynthesis-superparamagnetic-iron-oxide-and-iron-0