Curvature-based stroke rendering

This paper describes an algorithm that renders lines that have various thicknesses and have sharp tapered ends. This algorithm does not require any special information on each local point of a line. The thickness is determined by curvature and lengths from both ends. Therefore the algorithm is applicable in a variety of line rendering situations, such as 3D rendering engines for high quality cel-animation-like effects, reuse of geometrical data designed by CAD for advertising purposes, edge enhancement in a photo retouching process with edge detection methods and so on. In addition, using the generated varying thicknesses, we have developed algorithms for shading and embossing effects.     

Branched-chain Amino Acid Biosensing Using Fluorescent Modified Engineered Leucine/Isoleucine/Valine Binding Protein

A novel fluorescence sensing system for branched-chain amino acids (BCAAs) was developed based on engineered leucine/isoleucine/valine-binding proteins (LIVBPs) conjugated with environmentally sensitive fluorescence probes. LIVBP was cloned from Escherichia coli and Gln149Cys, Gly227Cys, and Gln254Cys mutants were generated by genetic engineering. The mutant LIVBPs were then modified with environmentally sensitive fluorophores. Based on the fluorescence intensity change observed upon the binding of the ligands, the MIANS-conjugated Gln149Cys mutant (Gln149Cys-M) showed the highest and most sensitive response. The BCAAs Leu, Ile, and Val can each be monitored at the sub-micromolar level using Gln149Cys-M. Measurements were also carried out on a mixture of BCAFAs and revealed that Gln149Cys-M-based measurement is not significantly affected by the change in the molar ratio of Leu, Ile and Val in the sample. Its high sensitivity and group-specific molecular recognition ability make the new sensing system ideally suited for the measurement of BCAAs and the determination of the Fischer ratio, an indicator of hepatic disease involving metabolic dysfunction.     

Electric field-associated deformation of polyelectrolyte gel near a phase transition point

The influence of de electric fields on sodium acrylate—acrylamide copolymer gel near a phase transition point in acetone—water mixtures containing NaOH was studied. In the mixtures free of NaOH, the shrunken-state gel near a phase transition point was not influenced by dc electric fields, while the swollen-state gel near it shrank from its part facing to the positive electrode in dc electric fields. In the presence of NaOH, unprecedented swelling of the shrunken-state gel has been observed. The swollen-state gel showed swelling or shrinking in the field. The type of deformation was determined by the concentration of NaOH. The drift of mobile ions played a role in the deformation. The shrinking occurred through the conformational change of polymer network caused by the drift. The swelling was observed by the change of the osmotic pressure based upon the ion concentration difference between the inside and the outside of a gel.     

Lipase-Catalyzed Esterification of Triterpene Alcohols and Phytosterols with Oleic Acid

Oleic acid esters of phytosterols (PSs) and triterpene alcohols (TAs), derived from rice bran, were synthesized using lipases under mild conditions. Some lipases, especially from Candida rugosa, type VII, showed very high substrate specificity towards both PSs and TAs, when a mixture of PS and TA (PS/TA mixture) was used as the substrate source. The maximum yield of PS esters was ca. 80 % in each case; however, the maximum yield of TA esters was much lower when the reaction was continued for 7 days. Due to the difficulty in purifying the esters obtained when the PS/TA mixture was used as source of substrate, free PSs and TAs were separated from the PS/TA mixture by silica-gel and reverse-phase chromatography prior to esterification. The pure PSs or TAs were esterified with oleic acid to obtain the corresponding esters with high purity. Differential scanning calorimetric analysis of the resulting esters revealed that their melting points ranged from 7.0 to 42 °C. These values were at least 100 °C lower than those of the free PSs and TAs.     

Preparation of polydiacetylene single crystals based on physical vapor growth technique

We have succeeded in obtaining 10-mm-size polydiacetylene (PDA) single crystals using the physical vapor growth technique followed by the irradiation of ultraviolet (UV) rays, for the first time. The variety of growth conditions, such as growth temperature, growth time, carrier gases, and flow rate of gases are examined. Especially, the growth temperature and growth time have clear effects on the quality of crystals. Morphologies and sizes with relation to the various growth conditions are also observed. They show only one type of plateletlike shape with a pair of large parallelopiped planes, regardless of variety of growth conditions. The crystal thickness was estimated as about 500 nm by the observation of atomic force microscopy. The solubility of diacetylene (DA) and PDA to some organic solvents, and the X-ray diffraction data indicate that the obtained crystals are single crystals.     

Fluorescence from poly(N-vinylcarbazole) in uniaxially stretched polymer films

Steady-state and time-resolved fluorescence properties of poly(N-vinylcarbazole) (PVCz) dispersed in a polystyrene (PS) cast film were studied under tensile loadings at room temperature. The excited monomer emission of PVCz located around 350 nm decreased with increasing applied tensile strain from 0 to 0.8%. The strain enhanced the emission which was ascribed to the partial-overlap excimer of PVCz in a 360–430 nm region. The emission due to the full-overlap excimer of PVCz between 430 and 500 nm was unchanged by the action of the tensile loadings. The ratio of fluorescence intensities at 375 nm and 345 nm I₃₇₅/I₃₄₅ was proportional to the applied strain. The time-resolved fluorescence study indicated that the lifetimes of the excited monomer and of the partial-overlap excimer were not affected by the strain. The obtained results mean that the strain applied to the PS matrix increases the partial-overlap conformation of two adjacent carbazolyl chromophores in a PVCz chain and suggest that PVCz is a useful probe for detecting residual strains in polymer matrices. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 66: 1569–1573, 1997     

Development of amperometric immunosensor using boron-doped diamond with poly(o-aminobenzoic acid)

An alternative method of a protein immunosensor has been developed at boron-doped diamond (BDD) electrode material. In order to construct the base of the immunosensor, o-aminobenzoic acid (o-ABA) was electropolymerized at an electrode by cyclic voltammetry. The poly-o-ABA-modified BDD was characterized by scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The XPS result found that carboxyl groups were formed at the electrode surface. The carboxyl groups were then used to covalently attach protein probes. The amperometric sensing of mouse IgG (MIgG) was selected as the model at the poly-o-ABA-modified BDD to compare to the poly-o-ABA-modified glassy carbon (GC) at the same condition. An antimouse IgG from goat (GaMIgG) was covalently immobilized at a poly-o-ABA-modified BDD electrode which used a sandwich-type alkaline phosphatase (ALP) catalyzing amperometric immunoassay with 2-phospho-L-ascorbic acid (AAP) as substrate. The ALP enzyme conjugated at the immunosensor can generate AAP to the electroactive species of ascorbic acid (AA), which can be determined by amperometric detection. The signal was found to be proportional with the quantity of MIgG. The limits of detection (LODs) of 0.30 (3 SD) and 3.50 ng mL(-1) (3 SD) for MIgG at BDD and GC electrodes were obtained. It also was found that the dynamic range of 3 orders of magnitude (1-1000 ng mL(-1)) was obtained at BDD, whereas at GC, the dynamic range was more narrow (10-500 ng mL(-1)). The method was applied to a real mouse serum sample that contains MIgG.     

Single-crystal solidification of new Co–Al–W-base alloys

Solidification processing of new high-temperature Co–Al–W-base single-crystals has been investigated. Single-crystal bars with compositions of Co–9.4Al–10.7W, Co–8.8Al–9.8W–2Ta and Co–7.8Al–7.8W–1.5Ta–4.5Cr (at%) were successfully grown with a conventional Bridgman process. Helical grain selectors resulted in [001] dendritic growth with primary dendrite arm spacings in the range of 278–364 μm. Segregation of constituent elements in the dendritic structure was very limited, compared to Ni-base single-crystals. Concentration profiles obtained by electron microprobe and analyzed via the Scheil equation indicate distribution coefficients for Co, Al, W and Cr that are close to 1. The distribution coefficient of Ta was approximately 0.6, indicating preferential segregation to the liquid during solidification. These observations collectively suggest that convective instabilities and freckle formation are unlikely to occur during solidification of single-crystals of this new class of high strength Co–Al–W-base alloys.