Self-organized inorganic nanoparticle arrays on protein lattices

Cavities formed by proteins have been utilized as the reaction chamber for the fabrication of a range of inorganic nanoparticles, providing control of the size of particles by limiting growth and preventing agglomeration. In crystal form, proteins construct molecular arrays that can provide regularly arranged sites for nanoparticles. Here we report the fabrication of nanometric iron and indium particles using ferritin, an iron-storage protein. The indium nanoparticles thus formed have uniform spherical shape with diameter of 6.6 +/- 0.5 nm, while the iron nanoparticles are somewhat irregular in shape (5.8 +/- 1.0 nm). Regular two-dimensional arrays of these nanoparticles are successfully produced by crystallizing ferritin molecules on a water-air interface using the denatured protein film method. The lattice constant of these nanoparticle arrays is 13 nm with hexagonal packing, and arrays of more than 1 microm in area can be obtained by transfer onto silicon wafer.     

Observation of HOPG by STM and contact AFM in various gas atmospheres under pressures up to 1.1 MPa

Apparatus comprising a scanning tunneling microscopy (STM) and an atomic force microscopy (AFM) has been developed for use under supra-atmospheres. Observations of highly oriented pyrolytic graphite (HOPG) were carried out by STM and contact AFM operating in air and various gas atmospheres (hydrogen, helium, neon and argon) under pressures up to 1.1 MPa. Atomic resolution images of the HOPG were obtained by STM in all the gas atmospheres studied. However, it was found that the presence of water vapor gave rise to a noise current at increased pressures. Using contact AFM, the atomic resolution in an argon atmosphere decreased with increasing pressure, while atomic images were obtained under the other gas atmospheres at 1.1 MPa.     

Effect of hydroxypropyl-beta-cyclodextrin on the degradation of pentachlorophenol by potassium monopersulfate catalyzed with iron(III)-porphyrin complex

A novel biomimetic catalytic system containing a supramolecular complex between iron(III)-tetrakis(p-sulfonatophenyl)porphyrin [Fe(III)-TPPS] and hydroxypropyl-beta-cyclodextrin (HP-beta-CD) was examined for the potassium monopersulfate catalyzed oxidation of pentachlorophenol (PCP). In the absence of HP-beta-CD, the percentage of PCP disappearance and the numbers of chlorine atoms released from PCP increased to 50% and 1.5 for a 1-day reaction period, respectively. However, in the presence of HP-beta-CD, the PCP completely disappeared and the number of chlorine atoms from PCP was increased to 3.1. o-Tetrachloroquinone, 2- and 4-hydroxyl-nonachlorodiphenyl ethers, and octachlorodibenzo-p-dioxin were detected among the oxidation products. In the absence of HP-beta-CD, the percentage of PCP conversion to oxidation products increased and then reached plateau. In the presence of HP-beta-CD, the amount of oxidation products produced initially increased for the first 10 min and thereafter decreased gradually. These results suggest that the addition of HP-beta-CD results in the further degradation of oxidation products. In addition, the mineralization of PCP to CO2 was investigated using 14C6-labeled PCP. After a 1-day reaction period, 24% of the 14C6-labeled PCP was converted to 14CO2 in the presence of HP-beta-CD, although significant 14CO2 generation was not observed in its absence. The effect of HP-beta-CD on the facilitation of PCP degradation can be attributed to the fact that the self-oxidation of Fe(III)-TPPS is prevented by the formation of a stable supramolecular complex between HP-beta-CD and Fe(III)-TPPS.     

Behaviour of HCH (1,2,3,4,5,6-hexachlorocyclohexane) residue in the aquatic environment

The monthly variation in HCH (1,2,3,4,5,6-hexachlorocyclohexane) residue levels in surface waters was investigated. The logarithms of monthly HCH concentrations described the wave, and the equation of the wave was calculated by the least squares method. The waves indicated maximum concentrations in summer and minimum concentrations in winter at each sampling site. The maximum concentration of HCH in each year decreased gradually. The amplitude of the wave at the reservoir was the smallest among sampling sites. The slope of the wave at the downstream sampling site was smaller than that at the upper stream. Maximum concentration of total HCH at each sampling site in 1985 is estimated from the equations; the concentrations at the upper streams will be about a thousandth or a hundredth of that at the downstreams. Also, the equations for β-and γ-HCH were calculated, and indicated that β-HCH was more persistent than γ-HCH in surface water. The ratio of β-HCH to total HCH in surface water is estimated to be about 60% in 1985.     

Structural,electrical and optical properties of r.f.-magnetron-sputtered SnO2:Sb film

The effects of gas composition, pressure and substrate temperature on the properties of relatively thick (0.2–0.8 μm) SnO₂ films deposited onto fused quartz substrates by r.f. magnetron sputtering are reported. The lowest resistivity of about 2 × 10^?3ωcm was attained for high rate deposition conditions of about $\text{1000}\text{A}\text{?}\text{min}{}^{\mathrm{?1}}$ on substrates at a temperature of 400°C in an atmosphere of 10% O₂. This value corresponds to a carrier density of 3 × 10²⁰cm^?3 and a mobility of 10 cm²V^?1s^?1. The crystal structure was found to be sensitive to all the above parameters. Low resistivity films showed a highly preferred orientation of (101) parallel to the substrate.