In this study, the colloidal stability and sedimentation behavior of crystalline particles (300nm) in various organic solvents have been investigated by means of a backscattered light flux profile (Turbiscan). The backscattered light flux profiles revealed that the nanoparticles were readily sedimented in water, methyl alcohol, and ethyl alcohol due to a flocculation-induced particle growth, while a particle coalescence and a sedimentation of the nanoparticles were hardly observed in isopropyl alcohol. The migration velocities of the particle were measured as around 6.15/min, 12.53 m/min, 6.51m/min, and 0.18m/min for water, methyl alcohol, ethyl alcohol, and isopropyl alcohol, respectively, showing a remarkably slow migration of the particles in isopropyl alcohol

The influence of several experimental parameters on the formation of stable Alloy 625 nanoparticles dispersion in ethanol was investigated. Several analyzing methods were applied, like transmission profiles measured by Turbiscan, transmission electron microscopy, X-ray diffraction, gas chromatography, and particle size analyzer. The correlation among the increase of particle sizes, caused by nanoparticle coalescence and collision, concentration of dispersant and time was presented and discussed. The optimum conditions for the formation of stable dispersion are evaluated.

The effects of compaction pressure and sintering temperature on the densification of Fe-40wt%Ni alloy nanoparticles were analyzed. The Fe-Ni nanoparticles were fabricated by an arc-discharge method and then, compacted at three different pressures and sintered at 550 to . Densification was completed at temperature as low as and high-pressure compaction was found to enhance densification. Densification behaviors and microstructure developments have been investigated through density measurements, electron microscopies, and hardness measurements.

Magnetic oxide-coated iron nanoparticles with the mean size ranging from 6 to 75 nm were synthesized by aerosol method using iron carbonyl as a precursor under the flowing inert gas atmosphere. Oxide shells were formed by passivation of asprepared iron particles. The influence of experimental parameters on the nanoparticles' microstructure, phase composition and growth behavior as well as magnetic properties were investigated and discussed in this study.

The nanoparticles were synthesized by photochemical deposition in a suspension system. The prepared products were characterized by means of XRD, Uv-vis and photoluminescence spectra (PL). Its photocatalytic activity was investigated by the decomposition of methylene blue (MB) solution under illumination of visible and ultraviolet light, respectively. Compared to , the photocatalytic activity of the as-prepared is obviously enhanced due to the decreasing recombination of a photoexcitated electron-hole pairs. The Mechanism in which photocatalytic activity is enhanced has been discussed in detail.

The effects of reaction temperature and precursor concentration on the microstructure and magnetic properties of nanoparticles synthesized as final products of iron acetylacetonate in chemical vapor condensation (CVC) were investigated. Pure phase was obtained at temperature above and crystallite size of nanoparticles decreased with lowering precursor concentration. Also, the coercivity decreases with decreasing crystallite size of nanopowder. The lowest coercivity was 7.8 Oe, which was obtained from the nanopowder sample synthesized at precursor concentration of 0.3M. Then, the crystallite size of nanoparticles was 8.8 nm.

The effects of several experimental parameters on the formation of stable Ni nanoparticles dispersion were investigated. The suspensions of Ni nanoparticles were produced in organic solvents using Hypermer KD-2 as a dispersant. The transmission profiles, particle size distribution, zeta potential, and visual inspection results were used to discuss the stability of the dispersion. The optimal conditions for the formation of stable dispersion are evaluated.

Laser pyrolysis is a very suitable method for the synthesis of a wide range of nanoparticles. A pilot unit based on this process has been recently developed at CEA. This paper reports results showing the possibility to produce SiC and nanoparticles at rates of respectively 1 and 0.2 kg/h and also the possibility to adjust the mean grain size of the particles and their structure by changing the laser intensity and reactants flow rates. First tests of liquid recovery have been also successfully performed to limit the risks of nanoparticles dissemination in the environement during their recovery.

Tin oxide nanoparticles (n-SnO and ) were synthesized by the inert gas condensation (IGC) method under dynamic gas flow of oxygen and argon at various conditions. Transmission electron microscopy (TEM) and X-ray diffraction (XRD) method were used to analysis the size, shape and crystal structure of the produced powders. The synthesized particles were mostly amorphous and their size increased with increasing the partial pressure of oxygen in the processing chamber. The particles also became broader in size when higher oxygen pressures were applied. Low temperature annealing at in air resulted to crystallization of the amorphous n-SnO particles to .

The influence of doping on the structural and morphological properties of the phosphor system, obtained ultrasonically via Spray Pyrolysis from common gadolinium and europium nitrate solutions, was studied. The particle morphology, crystalline and chemical structure were studied by XRD, SEM and EDS. TEM was applied in order to identify the structure and growth of "primary nanoparticles" and determine the presence of domains locally affected by "Moires Frames" and "Crystallite Size". The SADP allows determining the presence of a polycrystalline material with two phases in the "as-prepared" samples, and only an Ia3 phase along the thermal treatment.

In this study, the effects of the dispersants, i.e., Hypermer KD-2 and poly(l-vinyl-2-pyrrolidone) (PVP), and their concentration on the dispersion stability of Ni nanoparticles () in ethanol were investigated by using a visual inspection, a transmission profile (Turbiscan), and a zeta potential measurement. The transmission profiles measured by Turbiscan showed that the particle size increased over the entire height of the sample for suspensions with both the dispersants without showing any particle coalescence and sedimentation. The visual inspection also confirmed that the Ni suspensions with Hypermer KD-2 and PVP were very stable for more than a year. The zeta potential values varied from positive to negative with increasing the dispersant's concentration. The dispersion stability of the suspensions was not affected by both the dispersant's concentration and the zeta potential values. The observed suspension stability of Ni nanoparticles was attributed to the steric effect for the Hypermer KD-2 and to the bridging effect for the PVP.

생분해성 양쪽성 고분자를 이용하여 수용액에 존재하는 소수성 오염물질(페놀, 4-니트로페놀, 벤젠, 톨루엔) 및 중금속(Cs+,;Mg2+,;Cu2+,;Ni2+,;Cr3)을 제거하였다. 친수성을 띤 단량체로써 분자량이 서로 다른(1,100 그리고 5,000) methoxy poly(ethylene glycol) (MPEG)를 이용해 합성하였다. 투과실험 결과 상대적으로 분자량이 작은 MPEG를 이용해 합성한 경우보다 분자량이 큰 MPEG를 사용하였을 때 더 높은 제거율을 나타내었다. 한외여과공정을 이용해 오염물 없이 생분해성 나노파티클을 투과한 결과 나노파티클 용액의 농도가 100 mg/L 이상인 경우 나노 파티클 제거율은 98% 이상이었다. 소수성을 나타내는 오염원 제거시 소수성이 큰 오염원일수록 더 높은 제거율을 보였다. 또한 금속이온의 경우는 3가, 2가, 1가 이온의 순서로 제거율이 높았다.

1990년도 초반에 개발되어 나노분말의 제조 공정으로 집중적으로 연구되어온 화학기상응축공정은 고강도용 나노분말 소재이외에 기능성 자성재료로의 응용에 주로 이용되어 왔다. 최근에는 이러한 응용이외에 나노분말의 표면을 다양한 이종 소재로 응용하고자하는 나노캡슐(혹은 core/shell)화 제조 공정으로 진보되어 다양한 합금 시스템으로 발전하게 되었다. 특히 최근 Particles 2005, Surface Modification in Particle Tech