CONTINUOUS VACUUM DRYER FOR ENERGY SAVING

A continuous vacuum dryer for energy saving has been developed in order to produce dried foods without heat denaturation in the products. This drying method is suitable for heat sensitive I and highly viscous foods and can dry to 1 to 4% in moisture content with good quality at around 40°C in product temperature andin 5 -10 min a drying time. Feed material with high viscosity has to I have uniform distribution on the belt in the vacuum chamber to I keep a constant drying for which a special feed nozzle has been developed after considerabl~ testing. Heat transfer on the wet material in the dryer has occurred by both conduction and radiation because of the design so that the thermal efficiency in     

Preparation of phosphoric acid resins with large cation exchange capacities from macroreticular poly(glycidyl methacrylate-co-divinylbenzene) beads and their behavior in uptake of metal ions

In order to prepare phosphoric acid resins (RGPs) with large cation exchange capacities, effects of porosity and cross-linking of the precursory poly(glycidyl methacrylate-co-divinylbenzene) beads on their functionalization with phosphoric acid were studied. Two series of precursory copolymers were prepared: one was prepared by changing the amount of divinylbenzene (1–25 mol %) but by fixing that of isobutyl acetate (porogen) at 140 vol % per monomer mixture; the other by changing the amount of the porogen (40–160 vol %) but by fixing that of the cross-linker at 10 mol %. It was clarified that porosity of the precursors plays an important role in the functionalization. Highly porous precursors were functionalized with high efficiency; for example, even the precursors containing 10 mol % of divinylbenzene resulted in RGPs having cation exchange capacities as large as 6–7 meq/g, so long as BET specific surface areas of the precursors were greater than ca. 30 m²/g. The selectivity study has revealed that RGP exhibits the characteristic metal ion selectivity. Lithium ion was adsorbed in preference to sodium and potassium ions; and so-called hard Lewis acid cations, such as uranyl, ferric, and aluminum ions, are adsorbed even from strongly acidic media (1 < pH < 2). Among common divalent metal ions, in addition, the resin exhibits the highest selectivity toward lead ion. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 63: 1327–1334, 1997     

Carbon Dioxide Sensor Mechanism of Porous Hydroxyapatite Ceramics

Hydroxyapatite and Cl⁻ -containing hydroxyapatite powders are prepared and characterized. Reversible substitution of CO^2-₃ for OH⁻ at the surface is presumed to be responsible for the sensor function. The role of Cl⁻, which is necessary to realize the sensor function and is incorporated during soaking treatment, is considered as follows. It may reduce the strain caused by the incorporation of CO^2-₃ (which is larger than OH⁻), and, hence, promote the reversible substitution reaction. This behavior is presumed because Cl⁻ -containing hydroxyapatite samples exhibit sensor characteristics typical of CO₂ without any treatment.     

Remineralization effects of xylitol on demineralized enamel

We morphologically determined the effects of xylitol on the remineralization of artificially demineralized enamel. The samples were demineralized and then immersed in a remineralizing solution with or without 20% xylitol at 37 degrees C for 2 weeks. Samples were observed using contact microradiography, a multipurpose image processor (MIP) and a high-resolution electron microscope (HRTEM). Contact microradiography indicated that remineralization occurred in the surface and deep layers of samples immersed in a non-xylitol solution. Samples immersed in a xylitol solution demonstrated less mineralization in the outer 10 microm of the outermost surface layers, but more mineralization in the middle and deep layers, than was observed in the non-xylitol samples. The MIP evaluation indicated that remineralization was more prominent in layers at depths of 50-60 microm in the xylitol samples than in the non-xylitol samples. Observation of the xylitol samples by HRTEM revealed crystals of various sizes and irregular shapes with unclear crystal angles in the outermost surface layers. In the middle layers, they had thickened and angles of crystals are clear. These results indicate that xylitol can induce remineralization of deeper layers of demineralized enamel by facilitating Ca2+ movement and accessibility.     

Colorimetric chemosensor for ATP based on phthalimide-appended poly(2,5-dimethoxyaniline)

We have designed a colorimetric conjugated polymer (PDMAp) for selective ATP sensing based on poly(2,5-dimethoxyaniline) bearing phthalimide which can form hydrogen bonds with adenine. PDMAp have been synthesized via chemical oxidative polymerization with CSA and DDQ and dedoping with an aqueous ammonia solution. PDMAp was displayed to signal the colorimetric selective detection for ATP over various nucleotides such as ADP, AMP, CTP, TTP, and GTP in DMSO–water (9:1, v/v) mixture. The absorption spectral change can be attributed to a doping process of ATP to PDMAp through hydrogen bonds between phthalimide and adenine as well as electrostatic interactions between the phosphate group of ATP and the backbone of PDMAp.     

Anti‐windup synthesis for a model predictive control system

In this paper, an anti‐windup design problem for a model predictive control system is studied. The plant is assumed to be stable. First, we propose the structure of an output feedback model predictive controller with an anti‐windup compensator. Then we show a design method of the anti‐windup compensator that guarantees closed‐loop stability and improves the transient response. The design problem of the anti‐windup compensator is reduced to a linear matrix inequality (LMI) optimization problem. Further, it is shown that there always exists an anti‐windup compensator that ensures global asymptotic stability. © 2016 Institute of Electrical Engineers of Japan. Published by John Wiley & Sons, Inc.     

Agglomeration of particles by ac corona discharge

Improving the collection efficiency for particles smaller than 1 μm on every precipitator is important. We sought to improve the collection of these particles on an ESP due to particle agglomeration. Particles are charged by ac corona discharge in a precharger and agglomerated by a dc electric field in an agglomerator downstream of the precharger. Diesel exhaust particles were used as particulate matter for the experiments. The distribution of particle size was measured using a particle counter and a scanning electron microscope. By these methods, particles as small as 0.01 μm could be counted. Results showed the agglomeration between particles at ac corona discharge operating mode. The concentration of particles smaller than approximately 0.35 μm decreases, and that of particles larger than approximately 0.35 μm increases in the agglomerator. The agglomeration rate increases with increasing applied voltage, then saturates. These results may be due to the size distribution and to decrease of concentration by agglomeration. © 1999 Scripta Technica, Electr Eng Jpn, 130(1): 30–37, 2000     

Preparation of All Polyester‐Based Semi‐IPN Elastomers Containing Self‐Associative or Non‐Associative Guest Chains via Post‐Blending Cross‐Linking

Mechanical properties of semi‐interpenetrating polymer network (semi‐IPN) elastomers consisting of chemical networks and self‐associative/non‐associative guest chains are demonstrated. Amorphous low T_g polyesters with thiol side groups (PE‐SH) are first synthesized by melt polycondensation. PE‐SH are then converted to polyesters containing COOH side groups (PE‐COOH) and amide side groups (PE‐amide) through Michael addition reaction of thiol groups with acrylic acid and acrylamide, respectively. Homogeneous semi‐IPN elastomers are obtained by thermal cross‐linking for bulk mixtures of PE‐COOH and PE‐amide in the presence of diepoxy cross‐linkers, where COOH and epoxy groups are reacted to form chemical cross‐links while the amide units form self‐complementary hydrogen bonds. Another sample containing non‐associative chains is also prepared by using polyester with N,N‐dimethylamide units, instead of PE‐amide. Dynamic mechanical analysis reveals that guest chain incorporation systematically brings plateau modulus reduction and a unique relaxation with higher tan δ value depending on the fraction and nature of guest chains. Tensile properties are also affected by the fraction and nature of guest chains; the incorporation of hydrogen bonded chains are beneficial to enhance breaking elongation and toughness without the sacrifice of maximum stress. The knowledge found in this work will be thus beneficial for creating tough soft materials with damping applications.     

Construction of human monoclonal single-chain Fv antibodies against small-cell lung cancer by phage display libraries derived from cell-immunized SCID mice engrafted with human peripheral blood lymphocytes

In this study, we describe a phage display strategy to obtain human monoclonal single-chain Fv (scFv) antibodies binding target cancer cell surface proteins. By developing a cancer cell immunization protocol for SCID mice engrafted with human peripheral blood lymphocytes in combination with an antibody phage display method, we have isolated phage antibodies binding small-cell lung cancer cell line H889 by subtractive selection. One of the isolated scFv antibodies, 12EAb, recognized the E2 component of pyruvate dehydrogenase complex (PDC-E2) by immunoprecipitation according to MALDI-TOF MS analysis. Furthermore, we have confirmed the plasma membrane localization of PDC-E2 in small-cell lung cancer cells by immunocytochemistry and cell surface protein biotinylation, although PDC-E2 is usually located in the mitochondrial matrix. These results, including unique localization of identified antigens, were obtained by proteomic approaches. The present methods can be applied to generate human monoclonal scFv antibodies against tumor cells and to identify new molecular targets for immunotherapy and markers for diagnosis.     

Gain‐Scheduled Control via Switching of LTI Controllers and State Reset

This paper proposes a synthesis method of gain‐scheduled control systems that switch linear time‐invariant controllers according to hysteresis of the scheduling parameter. Stability and L₂‐gain analysis and synthesis methods for switched systems are applied to the switched gain‐scheduled control synthesis using reset of the controller state, where also the reset law is computed via linear matrix inequalities (LMIs). In addition to optimization of an upper bound of L₂‐gain, we reduce jumps of control input via an auxiliary optimization. Numerical examples are presented to illustrate the switched gain‐scheduled controller.