Effect of Nanoencapsulated Vitamin B1 Derivative on Inhibition of Both Mycelial Growth and Spore Germination of Fusarium oxysporum f. sp. raphani

Nanoencapsulation of thiamine dilauryl sulfate (TDS), a vitamin B1 derivative, was proved to effectively inhibit the spore germination of Fusarium oxysporum f. sp. raphani (F. oxysporum), as well as mycelial growth. The average diameter of nanoparticles was measured as 136 nm by being encapsulated with an edible encapsulant, lecithin, whose encapsulation efficiency was about 55% in containing 200 ppm of TDS concentration: the 100 ppm TDS nanoparticle solution showed a mycelial growth inhibition rate of 59%. These results were about similar or even better than the cases of treating 100 ppm of dazomet, a positive antifungal control (64%). Moreover, kinetic analysis of inhibiting spore germination were estimated as 6.6% reduction of spore germination rates after 24 h treatment, which were 3.3% similar to the case of treating 100 ppm of a positive control (dazomet) for the same treatment time. It was also found that TDS itself could work as an antifungal agent by inhibiting both mycelial growth and spore germination, even though its efficacy was lower than those of nanoparticles. Nanoparticles especially played a more efficient role in limiting the spore germination, due to their easy penetration into hard cell membranes and long resident time on the surface of the spore shell walls. In this work, it was first demonstrated that the nanoparticle of TDS not a harmful chemical can control the growth of F. oxysporum by using a lower dosage than commercial herbicides, as well as the inhibiting mechanism of the TDS. However, field trials of the TDS nanoparticles encapsulated with lecithin should be further studied to be effectively used for field applications.     

Photoelectrochemical kinetics and the relationship between photovoltage and light intensity for metal photoelectrodes coated with adsorbed dyes

It is shown that the inclusion of an excited state step in parallel with a ground state charge-transfer step for a photoelectrode comprising a metal coated with an adsorbed dye leads to a different photovoltage-light intensity expression from that previously derived by Hillson and Rideal[4] who assumed simple displacement of the ground state charge-transfer process by light. The Hillson and Rideal expression is shown to be a valid approximation when illumination of the electrode only slightly perturbs the electrodic charge-transfer reactions.     

Isosurfaces as deformable models for magnetic resonance angiography

Vascular disease produces changes in lumenal shape evident in magnetic resonance angiography (MRA). However, quantification of vascular shape from MRA is problematic due to image artifacts. Prior deformable models for vascular surface reconstruction primarily resolve problems of initialization of the surface mesh. However, initialization can be obtained in a trivial manner for MRA using isosurfaces. We propose a methodology for deforming the isosurface to conform to the boundaries of objects in the image with minimal a priori assumptions of object shape. As in conventional methods, external forces attract the surface toward edges in the image. However, smoothing is produced by a moment that aligns the normals of adjacent surface triangles. Notably, the moment produces no translational motion of surface triangles. The deformable isosurface was applied to a digital phantom of a stenotic artery, to MRA of three renal arteries with atherosclerotic disease and MRA of one carotid artery with atherosclerotic disease. Results of the surface reconstruction from the deformable model were compared with conventional X-ray angiography for the renal arteries. Measurement of the degree of stenosis of the renal arteries was within 12% +/- 6%. The deformable model provided improvements over the isosurface in all cases in terms of measurement of the degree of stenosis or improving the surface smoothness.     

Sixth International Conference ACID ROCK DRAINAGE 2003

CONFERENCE

Sixth International Conference ACID ROCK DRAINAGE 2003     

Si nanocolumns as novel nanostructured supports for enzyme immobilization

Silicon nanocolumns have been used as novel supports for the high-density immobilization of enzymes. Silicon nanocolumns with diameters of ca. 50-100 nm and a height of 1 micron were constructed using glancing angle deposition. The surfaces were successively treated with 3-aminopropyltriethoxysilane (APTES) and then with an amine reactive polymer, poly(ethylene-alt-maleic anhydride), to attach soybean peroxidase (SBP) to the support. Optimal coverage of APTES, polymer, and SBP was obtained for incorporation of enzyme onto the sidewalls of the nanocolumns. SBP immobilized on the silicon nanocolumns demonstrated an enhancement in biocatalytic activity of 160% over that of the enzyme immobilized on flat silicon wafers with the same projected area. The enzymatic activity decreased with progressive washes for both supports. This decrease in the activity of enzyme was found to be primarily due to the intrinsic deactivation of immobilized enzyme on the silicon surface. Designing nanocolumns with optimal dimensions, spacing, and surface chemistry may lead to the development of high-density arrays of proteins for applications in biotechnology.     

Sonochemical degradation of chlorinated hydrocarbons using a batch and continuous flow system

The sonochemical degradation of chlorinated hydrocarbons such as 1,1,1-trichloroethane, trichloroethylene and tetrachloroethylene in aqueous solution was carried out in the batch and continuous flow systems at an ultrasonic frequency of 100kHz under an air atmosphere. In the batch experiment, the rate of degradation follows the order 1,1,1-trichloroethane>tetrachloroethylene>trichloroethylene, and the chlorinated hydrocarbon were readily degraded by ultrasonic irradiation. The experiments in the continuous flow system were performed in the range of volumetric flow rate from 7 to 30 x 10(-3)lmin(-1). The conversion of the chlorinated hydrocarbons at a steady-state of reactor depended on the volumetric flow rate. The yield of Cl(-) (as a measurement of mineralization of chlorinated hydrocarbons) was 70-90% of the chlorine atoms in the parent chlorinated hydrocarbon molecules. From the viewpoint of the scale-up process, the sonochemical degradation of trichloroethylene was simulated in a three stage reactor, and the conversion (>99%) in a third stage reactor was showed the good results that can be satisfied a desired water quality standard.     

Distributed Control for 3D Metamorphosis

In this paper, we define Proteo as a class of three-dimensional (3D) metamorphic robotic system capable of approximating arbitrary 3D shapes by utilizing repeated modules. Each Proteo module contains embedded sensors, actuators and a controller, and each resides in a 3D grid space. A module can move itself to one of its open neighbor sites under certain motion constraints. Distributed control for the self-reconfiguration of such robots is an interesting and challenging problem. We present a class of distributed control algorithms for the reconfiguration of Proteo robots based on the goal-ordering mechanism. Performance results are shown for experiments of these algorithms in a simulation environment, and the properties of these algorithms are analyzed.     

Microstructure characterization of fibrous HAp-(20 vol.% t-ZrO2)/Al2O3-(25 vol.% m-ZrO2) composites by multi-pass extrusion process

Core-shell structured HAp-(t-ZrO₂)/Al₂O₃-(m-ZrO₂) composites were fabricated using a multi extrusion process. The shell of Al₂O₃-(m-ZrO₂) phases was selected due to their excellent biocompatibility and mechanical properties and the core was designed with t-ZrO₂ dispersed in the HAp matrix. The t-ZrO₂ and m-ZrO₂ particles (< 400 nm) were homogeneously dispersed in the HAp and Al₂O₃ phases, respectively. In the HAp-(t-ZrO₂) core region, a heavy strain field contrast was observed due to the mismatch of their thermal expansion coefficients. The values of relative density, bending strength and Vickers hardness of the third pass fibrous HAp-(t-ZrO₂)/Al₂O₃-(m-ZrO₂) composites, which were sintered at 1400 °C, were about 93%, 169 MPa, and 792 Hv, respectively.     

Effect of Conductive Particle Properties on the Reliability of Anisotropic Conductive Film for Chip-on-Glass Applications

This paper describes how the material properties of conductive particles in anisotropic conductive films (ACFs) affect the electrical conductivity and the reliability of ACF interconnections for chip-on-glass (COG) applications. For the conductive particles, Au/Ni-coated polymer particles with a 5-diameter were used. Two different types of conductive particles were characterized with respect to their mechanical and electrical properties, such as ball hardness, recovery behavior, and electrical resistance. In addition, two ACFs were fabricated in the form of a double-layered structure, in which the thickness of the ACF and a nonconductive film (NCF) layer were optimized to have as many conductive particles as possible on the bump after COG bonding. The electrical contact resistance of an ACF interconnection in a COG structure depends mainly on the electrical properties of conductive particles in the ACF. The electrical reliability of an ACF interconnection in a COG structure also depends more on the electrical properties than the mechanical properties of conductive particles under a high-temperature and humid condition. Conductive particles with a lower electrical resistance, higher mechanical hardness, and lower recovery rate show better reliability than conductive particles with a higher electrical resistance, lower mechanical hardness, and higher recovery rate. Cross-sectional scanning electron microscopic (SEM) pictures of a COG interconnection show the deformation of two different conductive particles after the reliability tests. The ACF interconnections in the edge or corner of a driver IC show less reliable joints due to high absorption of moisture.