Growth behavior of gold nanoparticles synthesized in unsaturated fatty acids by vacuum evaporation methods.

Physical vapor evaporation of metals on low vapor pressure liquids is a simple and clean method to synthesize nanoparticles and thin films, though only little work has been conducted so far. Here, gold nanoparticles were synthesized by vacuum evaporation (VE) methods in ricinoleic acid and oleic acid, two typical unsaturated fatty acids (UFAs). The two solvents formed black aggregates after deposition and then shrunk and finally disappeared with the progress of time. By transmission electron microscopy (TEM) images, nanoparticles in ricinoleic acids formed aggregates and then dispersed by time, while in oleic acid big aggregates were not observed in all timescales. From TEM images and small angle X-ray scattering (SAXS) measurements, the mean size of the nanoparticles was about 4 nm in both ricinoleic and oleic acids. UV-Vis spectra were also taken as a function of time and the results were consistent with the growth behavior presumed by TEM images. Air exposure had an influence on the behavior of the sample triggering the nanoparticle formation in both solvents. From control experiments, we discovered that oxygen gas triggered the phenomenon and nanoparticles function as a catalyst for the oxidation of the UFAs. It stimulates the phenomenon and in ricinoleic acid, specifically, electrons are transferred from riconleic acid to the gold nanoparticles, enhancing the surface potential of the nanoparticles and the repulsive force between their electronic double layers.

Low fragment polyatomic molecular ion source by using permanent magnets.

Electron-ionization-type polyatomic molecular ion source with low fragment was developed by using a pair of ring-shaped Sm-Co magnets. The magnets were placed forward and backward side of ionization part to confine electrons extracted from a thermionic cathode. Calculated electron trajectory of the developed ion source was 20 times longer than that of an ordinary outer filament configuration that has no magnetic confinement. Mass spectra of the molecular ions generated from n-tetradecane (C14H30) gas exhibited 4 times larger intensity than that of the ordinary configuration in a range of mass/charge from 93 to 210 u. This indicates that suppression of fragment ion was obtained by increase of low energy electrons resulted from the electron confinement.

Dependence of size distribution for liquid cluster ions on retarding voltage.

We have succeeded in producing liquid clusters such as ethanol and water clusters by an adiabatic expansion phenomenon, and the cluster size distribution was analyzed by using the time-of-flight method. For ethanol cluster ions, the size was distributed between a few hundreds and a few thousands, and the peak size was approximately 1200 molecules per cluster. For water cluster ions, the size distribution shifted to higher values, and the peak size was approximately 2500 molecules per cluster. Furthermore, the cluster size distribution was measured by changing the retarding voltage, and it was found that the minimum size increased with increase of the retarding voltage. In addition, the minimum size was larger than the critical size estimated by the theoretical calculation.

Physical and chemical sputterings of solid surfaces irradiated by ethanol cluster ion beams.

In order to clarify the interactions of ethanol cluster ion beams with solid surfaces, sputtering processes for Si, SiO(2) and Au surfaces were investigated by changing the acceleration voltage, the retarding voltage, and the incident angle. For the case of the normal incidence, the sputtered depth increased with increase of the acceleration voltage, and the sputtering ratio of Si to SiO(2) was approximately 10 at an acceleration voltage of 9 kV. Furthermore, with regard to the incident angle dependence, the sputtered depth for the Si surfaces had a maximum value at an incident angle between 10 degrees and 60 degrees . On the other hand, for the case of the physical sputtering by ethanol cluster ion irradiation on Au surfaces, the sputtered depth decreased with increase of the incident angle. With regard to the retarding voltage dependence, the sputtered depth had a maximum value for the Si surfaces, and the retarding voltage corresponding to the peak value changed according to the acceleration voltage applied. In addition, for the case of Au surfaces, the sputtered depth decreased with increase of the retarding voltage, and the physical sputtering was influenced by the minimum size of the cluster.

Apatite formation on titanium substrates by electrochemical deposition in metastable calcium phosphate solution.

An apatite layer was successfully formed on titanium substrates by electrochemical deposition in a metastable calcium phosphate solution, which had 1.5 times the ion concentrations of a normal simulated body fluid, but did not contain MgCl(2).6H(2)O, at 41 degrees C for 40 or 60 min at 13 mA. The current did not produce large effects on the crystalline size of the apatite, but the thickness of the apatite layer could be controlled by deposition conditions such as electrolyte temperature, current and deposition time. It is expected that the present electrochemical deposition will be useful to rapidly coat apatite on metallic materials.

PET fiber fabrics modified with bioactive titanium oxide for bone substitutes.

A rectangular specimen of polyethylene terephthalate (PET) was soaked in a titania solution composed of titanium isopropoxide, water, ethanol and nitric acid at 25 degrees C for 1 h. An amorphous titanium oxide was formed uniformly on the surface of PET specimen, but did not form an apatite on its surface in a simulated body fluid (SBF) within 3 d. The PET plate formed with the amorphous titanium oxide was subsequently soaked in water or HCl solutions with different concentrations at 80 degrees C for different periods of time. The titanium oxide on PET was transformed into nano-sized anatase by the water treatment and into nano-sized brookite by 0.10 M HCl treatment at 80 degrees C for 8 d. The former did not form the apatite on its surface in SBF within 3 d, whereas the latter formed the apatite uniformly on its surface. Adhesive strength of the titanium oxide and apatite layers to PET plate was increased by pre-treatment of PET with 2 wt% NaOH solution at 40 degrees C for 2 h. A two-dimensional fabric of PET fibers 24 microm in diameter was subjected to the NaOH pre-treatment at 40 degrees C, titania solution treatment at 25 degrees C and subsequent 0.10 M HCl treatment at 80 degrees C. Thus treated PET fabric formed the apatite uniformly on surfaces of individual fibers constituting the fabric in SBF within 3 d. Two or three dimensional PET fabrics modified with the nano-sized brookite on surfaces of the individual fibers constituting the fabric by the present method are believed to be useful as flexible bone substitutes, since they could be integrated with living bone through the apatite formed on their constituent fibers.