Inhibitory effect of lead on the proliferation of cultured vascular endothelial cells

We investigated the effect of lead nitrate (0.5, 1.0, 2.0 or 5.0 microM) on the proliferation of cultured bovine aortic endothelial cells. After exposure to lead, the number of cells and the incorporation of [3H]thymidine into the acid-insoluble fraction of the cells were reduced in parallel in a concentration-dependent manner. Histologically, lead treatment resulted in a decrease in the cell number accompanied by a change in the cell shape from polygonal to spindle; however, no degenerative change was observed except in 5.0 microM lead-treated cells. Furthermore, stimulation of [3H]thymidine incorporation by either basic or acidic fibroblast growth factor was significantly reduced by lead. However, the leakage of lactate dehydrogenase into the medium from the cells, a marker of nonspecific cell damage, was not changed by lead. From these results, it was revealed that lead inhibits the proliferation of cultured vascular endothelial cells without nonspecific cell damage. Although lead does not destroy the monolayer of endothelial cells, the metal may exhibit its noxious effect in the repair process of the vascular endothelium.     

Thermodynamic investigations of liquid Bi-Na and Sn-Na alloys by coulometric titration using β″-alumina

The following double galvanic cell was assembled and the thermodynamic properties of liquid Bi-Na and Sn-Na alloys, and the ion selectivity of -alumina during coulometric titration, were investigated. Mo, Na(I)¦-alumina¦M-Na(I), Mo [I] M-Na(I)¦-alumina¦Au + Au₂Na, Mo [II] (M = Bi or Sn) where M-Na(1) and Au + Au₂Na were used as the common electrode and reference electrode, respectively. Sodium was coulometrically titrated through the -alumina electrolyte of cell I both ways, and the EMFs were measured. It was found that no ion-exchange reaction occurs between the liquid alloys and the -alumina, and only Na was transferred in the -alumina during coulometric titrations. The thermodynamic properties of liquid Sn-Na and Bi-Na alloys were found to be in agreement with the literature.     

Superconducting properties of the lithium-substituted YBa2Cu4O8 prepared by the sol-gel method

The effects of the lithium substitution for copper on the properties of the superconducting YBa₂Cu₄O₈ were studied. Single-phase YBa₂Cu_4–x LixO₈ was successfully prepared by the sol-gel method under ambient pressure over a composition range of 0x 0.08, while impurity phases appeared at x=0.10 and 0.20. The lattice constants of YBa₂Cu_4–x Li _x O₈ were almost invariant with increasing lithium content x. The superconducting transition temperature decreased monotonically with increasing x in the range, 0x0.08. The suppression of superconductivity was discussed in terms of the impurity effect in the CuO₂ planes.     

Osmium-metal coating device using hollow-cathode plasma CVD method

A novel osmium-metal coating device for SEM observation has been developed to prevent negative charge build-up on specimens by applying the hollow-cathode low voltage discharge plasma chemical vapour deposition (CVD) method. The CVD method using the hollow-cathode offers the following advantages. (i) The method can deposit osmium-metal at very low discharge voltage that is as low as half of that of the planar parallel electrode method. Therefore, the method avoids damage due to ion bombardment during the coating process. (ii) The method can minimize the quantity of the OsO4 gas by introducing directly into the hollow-cathode. This feature is important to prevent the air pollution caused by the purged gas. (iii) A large coating area is guaranteed because the Os ion is filled in the hollow-cathode where the specimen is holed. (iv) The lower discharge voltage can be used by mixing Ar, N2 or air with the OsO4 gas as the environmental gas in the chamber. (v) The hybrid coating is also available by lining the appropriate metal material such as platinum (Pt) on the surface of the inside of the hollow-cathode. The method uses the plasma CVD of Os metal as well as the ion-sputter deposition of the lined metal.     

Preparation of Lead Lanthanum Zirconate Titanate (PLZT, (Pb,La)(Zr,Ti)O3) Fibers by Sol-Gel Method

Lead lanthanum zirconate titanate (PLZT, (Pb,La)(Zr,-Ti)O₃) ceramic fibers were prepared by the sol-gel method from a solution of lead acetate trihydrate, lanthanum isopropoxide, zirconium n -propoxide, and titanium isopropoxide that contained 2-methoxyethanol as the solvent. The sols obtained from the solution were concentrated at 156°-174°C for 2 h. Concentration at higher temperatures resulted in more-viscous sols of higher specific gravities. The concentration resulted in the formation of spinnable sols, which had viscosities >10⁵ mPas and exhibited Newtonian flow properties. These spinnable sols were formed to be so stable that no change in viscosity and spinnability was observed for more than three months when stored in a sealed container at room temperature. Gel-to-ceramic fiber conversion was investigated by means of X-ray diffractometry, infrared spectroscopy, and thermal analysis. Single-phase perovskite PLZT ceramic fibers 5-200 μm in diameter and >20 cm in length were obtained. Scanning electron microscopy (SEM) observation and Brunauer-Emmett-Teller (BET) measurement showed that heat treatment of the fibers at a lower rate resulted in the formation of fibers of denser microstructure. Although the SEM image of the cross section of the fibers revealed a relatively dense microstructure and a laser beam could be transmitted through a fiber 6 mm in length, BET measurement of the fibers indicated that the fibers had more than a few percent of open porosities, and scattering of light was observed in the laser-beam guiding test.     

Chemical durability of a superconducting oxide YBa2Cu3Ox in aqueous solutions of varying pH values

The chemical durability of a superconducting oxide YBa₂Cu₃O _x in the aqueous solution was investigated as a function of pH value by measuring the amount of leaching of the cations in the solution by inductively coupled plasma (ICP) analysis. The chemical durability of YBa₂Cu₃O _x was very low in highly acidic solutions of pH ca, 1, where the cations were dissolved in the same cation ratio as that of the compound. In an ion-exchanged water and NaOH solution, barium ions were leached out preferentially and almost no yttrium and copper ions were leached out. When NH₄OH was used as a basic reagent, the amounts of barium ions leached out were higher than in the NaOH solution of the same pH value and the dissolution of copper ions was observed, unlike in the NaOH solution of the same pH value. These observations were explained in terms of the chemical stability of individual oxide components.     

High-speed and low-driving-Voltage thin-sheet X-cut LiNbO/sub 3/ Modulator with laminated low-dielectric-constant adhesive

We present a novel thin-sheet X-cut LiNbO/sub 3/ optical modulator structure which can be fabricated by precise polishing and lapping to obtain a thinner LiNbO/sub 3/ substrate for a lower driving voltage in addition to velocity matching and impedance matching. We demonstrated that the fabricated modulator had a driving voltage V/spl pi/ of 2 V and zero chirp for 40-Gb/s operation and had a high potential for suppressed dc drift, and long-term reliability.     

Variation in In-Plane Stress during Densification and Crystallization of Titania Gel Coatings Deposited on Different Substrate Surfaces

Titania gel films were prepared from a coating solution with a starting mole ratio of Ti(OC₃H₇ⁱ)₄:H₂O:HNO₃:C₂H₅OH=1:1:0.2:30 on Si(100) wafers by spin coating, with and without sol–gel-derived, fired silica, and titania underlayers. In situ measurement was conducted on the in-plane stress in the titania gel films during heating up to 500°C at 5°C/min. Basically, for all the gel films, the in-plane, tensile stress increases once with increasing temperature, and then decreases around the temperature of crystallization. The increase in stress was thought to result from the capillary pressure due to solvent evaporation and from the densification of the coatings. The reduction in stress around the temperature of crystallization was ascribed to the accelerated atomic diffusion in the coatings and to the difference in thermal expansion coefficient between the coatings and the Si wafer. However, when the stress–temperature curves were examined more in detail, differences were found in the variation in stress, depending on the underlayers. Then, the question of how the underlayers could induce the crystallization and relax the strain in the coatings was discussed.     

Effects of the incorporation of silver and gold nanoparticles on the photoanodic properties of rose bengal sensitized TiO2 film electrodes prepared by sol-gel method

Rose bengal-deposited TiO₂ film electrodes bearing dispersed Ag or Au nanoparticles were prepared by the sol-gel method. The dye-induced visible region photoresponse of the electrodes decreased with increasing Ag content up to a mole ratio of Ag/TiO₂ = 0.0207, while the UV photoresponse increased. On the other hand, the dye-induced visible region photoresponse decreased to a less extent by incorporation of a larger amount of Au particles of Au/TiO₂ = 0.06, along with decreased UV photoresponse. The effects of the metal particles on the dye sensitization of the electrodes were discussed in terms of band edge fluctuation induced by the surface metal particles, Schottky barriers at TiO₂/metal interfaces, and surface plasma resonance.     

Perhydropolysilazane-derived silica-polymethylmethacrylate hybrid thin films highly doped with spiropyran: Effects of polymethylmethacrylate on the hardness, chemical durability and photochromic properties

Polymethylmethacrylate (PMMA)-perhydropolysilazane (PHPS) hybrid thin films doped with spiropyran were prepared by spin-coating, which were then converted into 0.26-1.7 μm thick, spiropyran-doped PMMA-silica hybrid films by exposure treatment over aqueous ammonia. The spiropyran/(spiropyran + PHPS + PMMA) mass ratio was fixed at a high value of 0.2 so that the films exhibit visual photochromic changes in color, while the PMMA/(PMMA + PHPS) mass ratio, r, was varied. The spiropyran molecules in the as-prepared films were in merocyanine (MC) and spiro (SP) forms, with and without an optical absorption at 500 nm, at low (r ≤ 0.2) and high (r ≥ 0.4) PMMA contents, respectively. When PMMA content r was increased from 0 to 0.2, the degree of the MC-to-SP conversion on vis light illumination was enhanced, while at higher r's the spiropyran molecules underwent photodegradation. When the silica film (r = 0) was soaked in xylene under vis light, the spiropyran molecules were almost totally leached out, while not on soaking in the dark. On the other hand, no leaching occurred for the film of r = 0.2 either in the presence or absence of vis light. These suggest that the introduction of PMMA is effective in improving the chemical durability of the films, while the silica film (r = 0) is an interesting material with a photoresponsive controlled-release ability. The pencil hardness of the films decreased with increasing PMMA content, but remained over 9H at r ≤ 0.4.