Synthesis and optical properties of azobenzene side chain polymers derived from the bifunctional fumaric acid and itaconic acid

Three type polymers containing the same azobenzene side chain group with different backbone structures, poly(DMAz6Fm), poly(DMAz6It) and poly(MAz6Ac) derived respectively from fumaric acid, itaconic acid and acrylic acid, were synthesized. The dependence of photo-response properties on the polymeric architecture was investigated for the solutions and films. By irradiation of the linearly polarized light (436 nm), uniaxial orientations of the thin films were induced and anisotropic properties were investigated by measurements of the order parameters and birefringence values.     

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.     

Catalytic behavior of AMoOx (A = Ba, Sr) in oxidation of 2-propanol

Perovskite-type oxides, BaMoO₃ and SrMoO₃, were prepared by reduction of scheelite-type oxides, BaMoO₄ and SrMoO₄, in H₂ flow at 873 K and characterized by XRD, TG, SEM, TPR, NH₃-TPD, UV-vis DRS and BET measurement. The catalytic activity of these alkaline-earth molybdenum oxide catalysts was tested for oxidation of 2-propanol with gaseous oxygen under atmospheric pressure. Dehydration to propylene was mainly promoted over the scheelite-type with Mo⁶⁺, while oxidative dehydrogenation to acetone was mainly promoted over the perovskite-type with Mo⁴⁺, and selectivity to acetone was much higher over BaMoO₃ than over SrMoO₃. Both perovskite-type oxide catalysts underwent oxidation to some degree during the catalytic reaction, so that they also contained some Mo⁶⁺. We concluded that the high selectivity to acetone resulting from oxidative dehydrogenation during 2-propanol conversion is related to the constantly changing oxidation state of the catalyst, resulting in coexistence of Mo⁶⁺ octahedra and Mo⁴⁺ octahedra on the AMoO₃ oxides.     

Effect of active oxygen species on the productivity of torularhodin by Rhodotorula glutinis No. 21

The effect of active oxygen species on the productivity of torularhodin, an effective antioxidant, by soil yeast, Rhodotorula glutinis no. 21, was examined. Methylene blue, methyviologen and AAPH [2,2'-azobis(2-amidinopropane) dihydrochloride] were used as generators of singlet oxygen, superoxide anion radicals and peroxy radicals, respectively. All of them indicated effectiveness at a dose of 1.0 x 10(-10) to 3.0 x 10(-6) M. Addition of these generators to the culture medium had almost no influence on the biosynthesis of beta-carotene, whereas it had marked enhancement on those of torulene and torularhodin. Production of uric acid by xanthineoxidase remained unchanged at a torularhodin concentration of up to 100 microM. This result suggests that torularhodin does not directly affect the productivity of superoxide anions. It has been proved that torularhodin has a more potent effect on the scavenging of peroxyl radicals and inhibits substrate degradation by singlet oxygen more effectively than beta-carotene does. Continuous addition of methylene blue enhanced the torularhodin accumulation more markedly than single addition.     

Detection method of the Kuroshio front using the satellite-derived chlorophyll-a images

Satellite-derived sea surface temperature (SST) has been providing high-resolution information of the oceanic front. However, in summer, increasing surface heating effects make SSTs uniform and the SST front disappears. The purpose of the present study is to examine applicability of satellite-derived surface chlorophyll-a (Chl-a) for detection of the Kuroshio front in the ocean south of Japan during the summer season.The Kuroshio surface front is formed between the Kuroshio water (KW) and the coastal water (CW) in the study area. Investigating accumulated in situ observations of SST and Chl-a, it is shown that the difference of Chl-a between KW and CW is increased in summer though that of SST becomes small. Using 76 pairs of cloud-free satellite-derived SST and Chl-a images with 0.01° spatial resolution, their seasonal variations are investigated through two-dimensional (2-D) histograms of Chl-a and SST. In summer, SST ranges from 25 to 30 °C and Chl-a ranges 0.03 to 0.4 mg/m³. Two peaks in the summer 2-D histogram correspond to wider KW and CW areas with rather uniform Chl-a and SST distributions. The peak values are extracted from the 2-D histograms and used to determine a threshold value dividing the KW and CW surface Chl-a during summer. It is found that the Chl-a concentration of 0.17 mg/m³ divides the extracted peaks into two groups, i.e., CW and KW except for a few peaks.The proposed Kuroshio-front detection method using the Chl-a images and the threshold value is examined using the satellite images and in situ data. The threshold contour superimposed in the summer Chl-a image distinctly separates the two representative waters in the ocean south of Japan. The front positions determined by the satellite-derived Chl-a, in situ SST, and in situ surface salinity transects along observation lines crossing the Kuroshio front agree with each other. Applying a traditional Kuroshio front index of temperature at 200 m depth, the capability of new Chl-a threshold in dividing two waters around the near-front area is quantitatively examined. Producing 74 match-ups of the satellite-derived Chl-a and 200-m temperature in the frontal zone, the dividing capability is evaluated quantitatively using the traditional Kuroshio-axis index. The detection capability of the proposed method is 82%, which can be considered high enough for practical applications.     

Error estimation of recursive orthogonal polynomial expansion method for large Hamiltonian system

Recursive polynomial expansion method is an efficient scheme to evaluate Green functions for large systems without direct diagonalization of the Hamiltonian. It is based on a polynomial expansion of the Green function, and has many advantages compared with other methods. However, there are little reports on its error estimations. In this paper, the cut-off error of the method is estimated analytically, which results from the truncation of expansion at finite orders. It is found that the error is inversely proportional to the number of expansion order N except for the singular points for the system with point spectrum. For the system with continuous spectrum, the error is inversely proportional to N^3/2 and decreases much faster in terms of the expansion order.     

Active centers, catalytic behavior, symbiosis and redox properties of MoV(Nb,Ta)TeO ammoxidation catalysts

Selective as well as waste forming active centers were defined for MoVNbTeO and MoVTaTeO catalysts in the ammoxidation of propane to acrylonitrile and all catalytic functionalities were assigned to specific elements at the respective active centers. Symbiosis between M1 and M2 phases of these catalysts was observed, with phase cooperation being more extensive in the Nb than Ta containing compositions. The difference in catalytic effectiveness arises most likely because contact and surface area exposure of the two respective, cooperating phase pairs are not equal. The M1 phase of the catalysts is reducible by propane and ammonia in the absence of dioxygen and is regenerable to its original, fully oxidized state by dioxygen (air). No structural collapse is observed even after 120 C₃H₈ + NH₃ reduction pulses. The so induced reduction of the catalyst extends up to 70 layers deep. The product distribution over the first few pulses is very similar to that under catalytic conditions, supporting the concept that lattice oxygen is involved in the catalytic ammoxidation process. Therefore, the ammoxidation of paraffins is a redox process, as is of course the well-known olefin ammoxidation process.