[1] Mass concentrations of elemental carbon (EC) in fine mode and mixing ratios of carbon monoxide (CO) were measured at the University of Tokyo campus in Tokyo in different seasons in [2003][2004][2005]. Measurements of EC were made using a semicontinuous thermal-optical analyzer. The mass concentrations of nonvolatile aerosol measured by the calibrated scanning mobility particle sizer combined with a heated inlet agreed with the independent EC measurements with a systematic difference of about 4%, demonstrating that the mass concentrations of nonvolatile aerosol well represent those for EC. A majority of the nonvolatile aerosol and therefore EC mass concentration was in volume equivalent diameters between 50 and 200 nm, peaking at around 130 nm. The correlation of EC and CO was generally compact throughout the measurement period because of the similarity in sources. The slope of the EC-CO correlation (DEC/DCO) is therefore a useful parameter in validating EC emission inventories. The EC concentration and DEC/DCO showed distinct diurnal variation. On weekdays, EC and DEC/DCO reached maximum values of about 3 mg m À3 and 9 ng m À3 /parts per billion by volume, respectively, in the early morning (0400-0800 local time), when the traffic density of heavy-duty trucks with diesel engines was highest. In addition, these values were lower by a factor of 2 on Sundays. The heavy truck traffic showed similar diurnal and weekday/weekend variations, indicating that exhaust from diesel engines is an important source of EC. Monthly mean DEC/DCO showed a seasonal variation, reaching broad maximum values in spring-autumn and reaching minimum values in midwinter, following the seasonal variation in temperature, as observed in Maryland, United States (Chen et al., 2001). This temperature dependence is likely due to the temperature dependence of EC emissions from diesel engines on intake air temperature. More stringent regulation of emissions of particles from diesel cars started in the Tokyo Metropolitan Area in October 2003. The DEC/DCO values did not change, however, exceeding the natural variability (10%) after 1 year from the start of the new regulations, when the temperature dependence is taken into account. This indicates that the regulation of particle emissions in the Tokyo Metropolitan Area was not effective in reducing the EC concentrations after 1 year.

[1] Semicontinuous measurements of water-soluble organic carbon (WSOC) and organic carbon (OC) in PM 2.5 were made at Gosan, Korea, in March-April 2005. On average, the WSOC/OC mass ratio for all air masses observed at Gosan was 0.30 ± 0.12. WSOC correlated well with CO (r 2 = 0.54) in Chinese outflow, suggesting that a major part of the observed WSOC and/or their precursors was of combustion origin. The relationship between the increase of WSOC and O 3 suggests that the observed WSOC was mostly secondary product. To interpret the measured organic compounds, thermal analyses of organic standards were made in the laboratory. Thermograms of a single standard of water-soluble organic species showed that carbon that evolved at high temperatures (600°-870°C) was generally associated with water-soluble compounds having high molecular weights (MWs) on the order of hundreds, while carbon that evolved at low temperatures (<300°C) generally had MWs of less than $180 g mol À1 . Positive matrix factorization (PMF) analysis revealed three organic compound groups (low, medium, and highly refractory compounds) based on the OC thermograms. On average, highly and low refractory compound groups accounted for 79% and 21% of the WSOC mass, respectively, at Gosan. Highly refractory compound groups significantly contributed to WSOC regardless of air mass origin. The results of the laboratory experiments imply that a large fraction of these highly refractory compound groups was likely associated with high MW compounds. For water-insoluble organic carbon(=OC-WSOC), medium and low refractory compound groups accounted for 60% and 40%, respectively, consistent with the results of the laboratory experiments.

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A modified polyol process for the synthesis of cubic‐shaped FeCo particles at 403 K is demonstrated. Control of the particle composition and size was achieved by varying the experimental conditions. The Fe content in the FeCo particles can be varied from 90 to 20 mol %, and the size of the cubes can be controlled to obtain particles with sizes between 300 and 35 nm (see figure). The magnetic properties of the particles closely resemble those of bulk FeCo.

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A layer-by-layer assembly composed of avidin and 2-iminobiotin-labeled poly(ethyleneimine) (ib-PEI) was prepared on the surface of a platinum (Pt) film-coated quartz resonator, and an electrochemically induced disintegration of the avidin-ib-PEI assembly was studied using a quartz crystal microbalance. The resonance frequency of a five-bilayer (avidin-ib-PEI)5 film-coated quartz resonator was increased upon application of an electric potential to the Pt layer of the quartz resonator, suggesting that the mass on the quartz resonator was decreased as a result of disintegration of the (avidin-ib-PEI)5 film, due to a pH change in the vicinity of the surface of the Pt-coated quartz resonator. It may be that the (avidin-ib-PEI)5 film assembly was decomposed by acidification of the local pH on the surface of the Pt layer, which in turn was induced through electrolysis of water on Pt, because ib-PEI forms complexes with avidin only in basic media. In pH 9 solution, the (avidin-ib-PEI)5 film was decomposed under the influence of an applied potential of 0.6-1.0 V versus Ag/AgCl. The (avidin-ib-PEI)5 film was decomposed almost completely within a minute in a low concentration buffer (1 mM, pH 9), while the decomposition was slower in 10 and 100 mM buffer solutions at the same pH. The decomposition of the assembly was rapid when the electrode potential was applied in pH 9 solutions, while the response was relatively slow in pH 10 and 11 solutions. All the results are rationalized on the basis of an electrochemically induced acidification of the local environment around the (avidin-ib-PEI)5 film on the Pt layer.

Luminescence properties of EuIII, TbIII, GdIII and NdIII complexes with a hexadentate ligand (abbreviated to EuL, TbL, GdL, and NdL, respectively), which have two bipyridine moieties bridged by an ethylenediamine unit, have been examined in acetonitrile and in the solid state.