Biochip with integrated pumps for plug-based sequential exchange of solutions

A novel method for exchanging solutions used in biochemical analyses and a device to carry out the exchange are proposed. An array of plugs formed using six injectors was transported in a microflow channel using a main pump located at one end of the main flow channel. The injectors and main pump were operated on the basis of the change in volume caused by the electrolysis of water. Bubbles were produced from working electrodes; these bubbles caused a diaphragm placed below the injectors to inflate and occlude the inlet of the solution reservoir. Increase in the number of bubbles caused the reservoir to inject the solution into the main flow channel in the form of a plug. Each plug was individually transported downstream to the sensing area by the main pump, which was operated in a similar manner to the injector. The device was used for the detection of a tumor marker, α-fetoprotein (AFP). Plugs of necessary solutions were individually transported to the sensing area with immobilized primary antibodies to allow antigen–antibody binding, cleaning, and detection. The fluorescence intensity from the antibodies showed clear dependence on the concentration of AFP. The immobilization of antibodies could also be carried out on-chip.     

Rate of emulsion polymerization of styrene

In emulsion polymerization, the Smith and Ewart theory gives about two or three times the number of polymer particles obtained by experiment. In this paper, a reaction model is proposed which, from the standpoint of reactor design, can give an adequate explanation of the whole course of an emulsion polymerization of monomer highly insoluble in water. Among other things, the generating process of polymer particles is examined in detail. It is demonstrated experimentally that a new parameter proposed here, which represents the degree of difficulty of monomer initiation in micelles, is indispensable in explaining that process. Also confirmed is that monomer initiation takes place more easily in polymer particles than in micelles. According to the new model, the progress of polymerization, i.e., monomer conversion, the number of the polymer particles, and properties of polymer thus produced can be estimated with satisfactory accuracy. Furthermore, approximate equations are derived for easier estimation.     

Conceptual core design of Advanced Recycling Reactor based on mature technologies

This paper presents about comprehensive investigations into Advanced Recycling Reactor (ARR) based on existing and/or mature technologies (called “Early ARR”), aiming transuranics (TRU) burning and considering harmonization of TRU burning capability, technology readiness, economy and safety. The ARR is a 500 MW_e (1180 MW_th) oxide fueled sodium cooled fast reactor, which the low core height of 70 cm and the large structure volume fraction with 1.0 mm of cladding thickness to tube wall have been chosen among 14 candidate concepts to reduce the TRU conversion ratio (CR) and the void reactivity, taking technology readiness into account. As a result of nuclear calculation, the ARR has TRU burning capability from 19 to 21 kg/TW_thh and is sustainable in recycling. And the ARR can accept several kinds of TRU; the LWR uranium oxide fuels, LWR-MOX used nuclear fuel, and TRU recycled in this fuel cycle and the ARR is also flexible in TRU management in ways that it can transform from TRU CR of 0.56 to breeding ratio (BR) of 1.03. In addition, it has been confirmed that the ARR core conforms to the set design requirements; the void reactivity, the maximum linear heat rate, and the shutdown margin of reactivity control system. It has been confirmed that the closed fuel cycle with the ARR plants of 180 GW_th will not release TRU outside and generate more electricity by 65% compared with the present nuclear power system in the US, curbing the risk of nuclear proliferation. Thus the study can conclude that the Early ARR is able to close nuclear fuel cycle, using mature technologies and has features of the sustainability in recycling, and the accommodation of almost all the TRU at present and in the future, and the flexibility in TRU management with breakeven core.     

Evaluation of theoretical critical angle including mass effects for channeling by computer simulation

The calculated critical angles using the theory included mass effects of Zheng et al. for the axial channeling of ion have been investigated by the computer simulations, making comparisons with the theory of Lindhard and the precise formula of Barrett’s numerical simulations. The computer simulations employing the ACOCT program code, which treats the atomic collisions three-dimensionally and is based on the binary collision approximation (BCA), were carried out for the channeling of He, Ne, Ar, Kr, Xe and Rn ions incident along the 〈1 0 0〉 axis in Al, Cu, Ag and Pt crystals. A slight dependence of the channeling critical angle on the atomic number of incident ion in the ACOCT results is in agreement with that in the calculated ones using the theory of mass effects. The average critical angles in the ACOCT results for the channeling of six rare gas ions are approximately 5.0/Z₂ times the magnitude of the theoretical critical angles with mass effects, where Z₂ is the atomic number of crystal atom. Besides, the results show that the calculated critical angles using the theory with mass effects are substantially larger than those using the theory of Lindhard, the Barrett’s formula and the formula by the ACOCT simulations for He ions impinging on Al, Cu, Ag and Pt crystals, and that the channeling critical angles in the ACOCT results agree well with those in the calculated ones using Barrett’s formula for 0.6-50 MeV He ions incident on Cu and Ag crystals and 5-50 MeV He ions impinging on Al and Pt crystals.     

Effects of manufacturing conditions on the properties of coal-derived caking additives

Manufacturing conditions of coal-derived caking substances (SRC) were investigated to determine the effects of these conditions on the chemical and caking properties of the additives. The solvent-refined coal (SRC) produced in the early stage of digestion at the lower temperature, of which β- and γ-fractions were 55 and 35 wt %, respectively, consisted of a heterogeneous mixture characterized by a low aromaticity, long side-chains, and a large, average molecular weight. The Roga index of the SRC was large but its total dilatation was small. As the digestion proceeded, the condensation and the cycloaromatization reactions improved the homogeneous nature and decreased the molecular weight by the breakage of side-chains, dealkylation, and deoxidation, leading to increases in the γ-fraction and total dilation by decreases in the β-fraction and Roga index. Such trends were more marked when the conversion exceeded 90 wt %. The relation between structure and the caking properties of the SRC are discussed.     

An extreame disposition method for low-level radioactive wastes using supercritical water (3)

Disposition of low-level radioactive wastes has been performed in supercritical water with RuO₂ as a catalyst without the addition of any oxidizing materials. These wastes arose from nuclear power plants etc., constituting of nonflammable organic materials, such as fire resistant sheeting and rubber gloves. We investigated the distribution behavior of iron and cobalt attached to nonflammable organic materials, in solid, liquid and gas phases during the decomposition of this method. The distributions of these elements under various conditions (initial amounts) were determined by using their radioisotopes as simulated low-level radioactive wastes in order to ease the detection of trace amounts of elements even in solid and gas phases. Iron and cobalt were found only in the solid phase when non-radioactive iron hydroxide was added as a precipitation reagent before the supercritical-water reaction.     

Measurement of large negative reactivity of an accelerator-driven system in the Kyoto University Critical Assembly

Large negative reactivity of a subcritical system driven by a pulsed 14 MeV neutron source has been measured in the Kyoto University Critical Assembly. The subcriticality of the accelerator-driven system (ADS) ranged in effective multiplication factor roughly from 0.98 to 0.92, which corresponded to an operational range of an actual ADS proposed by Japan Atomic Energy Agency. As the measurement technique, pulsed neutron method, power spectral analysis for pulsed neutron source, accelerator-beam trip method were employed. From neutron count decay data obtained by the pulsed neutron experiment, not only the prompt-neutron decay constant of fundamental mode but also a higher spatial mode could be derived. The subcriticality was also determined from the fundamental decay constant. The measured cross-power spectral density consisted of a familiar correlated reactor-noise component and many uncorrelated delta-function-like peaks at the integral multiple of pulse repetition frequency. The fundamental prompt-neutron decay constant, i.e., the subcriticality determined from the latter uncorrelated peaks was consistent with that obtained by the above pulsed neutron experiment. However, the magnitude of the former correlated component was reduced with an increase in the subcriticality and eventually this component became almost white at deeply subcritical state ranging in the multiplication factor under 0.95. Consequently, the determination of the decay constant from the correlated component was impossible under such a subcritical state. As data analysis method for the beam trip experiment, both the conventional integral count method and the least-squares inverse kinetics method (LSIKM) were employed. The LSIKM analysis led to the consistent subcriticality with that obtained by the pulsed neutron experiment, while the integral count method significantly underestimated the subcriticality. This underestimation originated from a residual background count, which was maintained after the beam trip. The LSIKM was mostly not influenced by such a slight count rate.     

Thermal response in thermal energy storage material around heat transfer tubes: effect of additives on heat transfer rates

The effects of carbon-fiber chips and carbon brushes as additives on the thermal conductivity enhancement of phase change materials (PCMs) using in latent heat thermal energy storage are investigated experimentally and numerically by considering the wall effect of the additives. The carbon-fiber chips are effective for improving the heat transfer rate in PCMs. However, the thermal resistance near the heat transfer surface is higher than that for the carbon brushes. As a result, the overall heat transfer rate for the fiber chips is lower than that for the carbon brushes. Consequently, the carbon brushes are superior to the fiber chips for the thermal conductivity enhancement under the present experimental conditions. The carbon brushes are moreover applied to the packed beds of particles to overcome their low thermal conductivity in chemical heat pump/storage. The carbon brushes essentially improve the heat transfer characteristics in the packed beds, though the thermal resistance is observed because the particles obstruct contact between the fibers and the heat transfer surfaces.     

Simultaneous Oxidization of NOx and SO2 by a New Non-thermal Plasma Reactor Enhanced by Catalyst and Additive

The non-thermal plasma as one of the most promising technologies for removing NOx and SO2 has attrm~ted much attention. In this study, a new plasma reactor combined with catalyst and additive was developed to effectively oxidize and remove NOx and SO2 in the flue gas. The experimental results showed that TiO2 could improve the oxidation efficiency of SO2 in the case of applying plasma while having a negative effect on the oxidation process of NO and NOx. With the addition of NH3, the oxidation rates of NOx, NO and SO2 were slightly increased. However, the effect of adding NH3 on NOx oxidation was negative when the temperature was above 200℃.