Contrasting diurnal variations in fossil and nonfossil secondary organic aerosol in urban outflow, Japan

Diurnal variations of fossil secondary organic carbon (SOC) and nonfossil SOC were determined for the first time using a combination of several carbonaceous aerosol measurement techniques, including radiocarbon (1?C) determinations by accelerator mass spectrometry, and a receptor model (chemical mass balance, CMB) at a site downwind of Tokyo during the summer of 2007. Fossil SOC showed distinct diurnal variation with a maximum during daytime, whereas diurnal variation of nonfossil SOC was relatively small. This behavior was reproduced by a chemical transport model (CTM). However, the CTM underestimated the concentration of anthropogenic secondary organic aerosol (ASOA) by a factor of 4-7, suggesting that ASOA enhancement during daytime is not explained by production from volatile organic compounds that are traditionally considered major ASOA precursors. This result suggests that unidentified semivolatile organic compounds or multiphase chemistry may contribute largely to ASOA production. As our knowledge of production pathways of secondary organic aerosol (SOA) is still limited, diurnal variations of fossil and nonfossil SOC in our estimate give an important experimental constraint for future development of SOA models.     

防冻型黏土质可塑料的研制

为了提高可塑料的抗冻结能力,以粒度为6～3、3～1、≤1 mm的焦宝石(w(Al2O3)>45%,w(SiO2)<52%)和粒度≤45μm的黏土(w(Al2O3)>26%,w(SiO2)<65%)为原料,加入硫酸铝溶液、水和乙二醇防冻液制备出防冻型黏土质可塑料.将试样放入零下15℃的试验箱中冷冻,在室温下放置至室温,再经110℃干燥和1 000℃热处理后,分别测试试样的线变化率、抗折强度、耐压强度和体积密度,并与常温20℃下放置的试样的各项性能加以比较.结果表明:试样经过110℃和1 000℃热处理后,普通可塑料试样在零下15℃冻结后的强度比正常未冻结试样的下降约20%,而防冻型可塑料与正常试样相比,在强度方面几乎没有改变.     

Transient phenomena of current and field distortion due to dynamics of packet‐like charges in LDPE films

Simultaneous measurements of space charge and external current were carried out using a PEA measurement system with an electrometer on the back of a grounding electrode in order to clarify the physical situation of a huge packet of positive space charges in LDPE films. A large number of positive charges from a semiconducting anode were accumulated at the interface between LDPE and an Al‐cathode at a mean applied field of 1.5 MV/cm and then finally disappeared. The results of simultaneous measurements showed that the external current kept a relatively high value during charge accumulation and further increased when the charges disappeared. Both the charge dynamics and the external current were restricted by addition of a low‐molecular‐weight paraffin wax, indicating that carrier transport was influenced by the microstructure of the polymer. The dynamics of the residual charges after short‐circuiting is also discussed. © 2012 Wiley Periodicals, Inc. Electr Eng Jpn, 179(4): 10–17, 2012; Published online in Wiley Online Library ( wileyonlinelibrary.com ). DOI 10.1002/eej.21256     

Further Characterization of 394-GHz Gyrotron FU CW GII with Additional PID Control System for 600-MHz DNP-SSNMR Spectroscopy

A 394-GHz gyrotron, FU CW GII, has been designed at the University of Fukui, Japan, for dynamic nuclear polarization (DNP)-enhanced solid-state nuclear magnetic resonance (SSNMR) experiments at 600-MHz ¹H resonant frequency. After installation at the Institute for Protein Research (IPR), Osaka University, Japan, a PID feedback control system was equipped to regulate the electron gun heater current for stabilization of the electron beam current, which ultimately achieved stabilization of output power when operating in continuous wave (CW) mode. During exploration to further optimize operating conditions, a continuous tuning bandwidth of approximately 1 GHz was observed by varying the operating voltage at a fixed magnetic field. In the frequency range required for positive DNP enhancement, the output power was improved by increasing the magnetic field and the operating voltage from their initial operational settings. In addition, fine tuning of output frequency by varying the cavity cooling water temperature was demonstrated. These operating conditions and ancillary enhancements are expected to contribute to further enhancement of SSNMR signal.     

Development of high performance Raney Cu-based catalysts for methanol synthesis from CO2 and H2

Catalytic hydrogenation of CO₂ into methanol has been investigated over Raney Cu-based catalysts. The Raney catalysts leached in NaOH/ZnO solutions showed high activities and selectivities for methanol synthesis. The deposition of Zn on the surface of Cu particles increased the surface area and the specific activity of Raney Cu–M. Raney Cu–Zr developed was significantly more active than a commercial catalyst.     

Characterization of the ybdT gene product of Bacillus subtilis: Novel fatty acid β-hydroxylating cytochrome P450

We have characterized the gene encoding fatty acid α-hydroxylase, a cytochrome P450 (P450) enzyme, from Sphingomonas paucimobilis. A database homology search indicated that the deduced amino acid sequence of this gene product was 44% identical to that of the ybdT gene product that is a 48 kDa protein of unknown function from Bacillus subtilis. In this study, we cloned the ybdT gene and characterized this gene product using a recombinant enzyme to clarify function of the ybdT gene product. The carbon monoxide difference spectrum of the recombinant enzyme showed the characteristic one of P450. In the presence of H₂O₂, the recombinant ybdT gene product hydroxylated myristic acid to produce β-hydroxyristic acid and α-hydroxymyristic acid which were determined by high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry. The amount of these products increased with increasing reaction period and amount of H₂O₂ in the reaction mixture. The amount of β-hydroxyl product was slightly higher than that of α-hydroxyl product at all times during the reaction. However, no reaction products were detected at any time or at any concentration of H₂O₂ when heat-inactivated enzyme was used. HPLC analysis with a chiral column showed that the β-hydroxyl product was nearly enantiomerically pure R-form. These results suggest that this P450 enzyme is involved in a novel biosynthesis of β-hydroxy fatty acid.     

Catalytic reforming of natural gas for hydrogen production in a pilot fluidized-bed membrane reactor: Mapping of operating and feed conditions

A fluidized-bed membrane reformer was operated in two independent laboratories to map various operating conditions, to investigate the effects of changing the composition of the natural gas feed stream and to verify earlier experimental trials. Two feed natural gases were tested, containing either 95.5 or 90.1 mol% of methane (3.6 or 9.9 mol% of other gaseous higher hydrocarbons). Experimental tests investigated the influence of total membrane area, reactor pressure, permeate pressure and natural gas feed rates. A permeate-H₂-to reactor natural gas feed molar ratio >2.3 was achieved with six two-sided membrane panels under steam reforming conditions and a pressure differential across the membranes of 785 kPa. The total cumulative reforming time reached 395 h, while hydrogen purity exceeded 99.99% during all tests.     

Inhibition effect of CO on hydrogen permeability of Pd–Ag membrane applied in a microchannel module configuration

The surface adsorption effect of CO on the hydrogen permeability of a 12.5 micron-thick Pd₇₇Ag₂₃ membrane has been evaluated quantitatively under experimental conditions close to the operating conditions of the highly-efficient membrane reformer (MRF) system developed by Tokyo Gas. The permeability of the membrane was measured in the conditions of CO concentration between 1 and 5 vol.% at a temperature and pressure of up to 500 °C and 0.6 MPa, respectively. High feed flow rates and a microchannel module configuration were applied in the flux measurements to ensure that the results are obtained with limited influence of concentration polarization adjacent to the membrane surface and hydrogen depletion along the microchannel length. While the CO inhibition effect was close to negligible at 500 °C, it was significant at lower temperatures. At a feed pressure of 0.2 MPa, the CO inhibition effect was only 0.2% at a CO concentration of 1 vol.% and the effect was 3.6% at a CO concentration of 5 vol.% at 500 °C. The CO inhibition effect were 3.4% for 1 vol.% CO and 14.1% for 5 vol.% CO at 400 °C. Measurements were also carried out at a high feed pressure of 0.6 MPa to evaluate the pressure dependence of the CO inhibition effect. The CO inhibition effect decreased to 0.7% at a CO feed concentration of 5 vol.% at 500 °C. Lower CO inhibition effect were also observed at 450 and 400 °C compared to the data obtained with the feed pressure of 0.2 MPa, while the inhibition levels were almost the same at 350 °C. Though the CO inhibition effect is larger at a lower feed pressure of 0.2 MPa, the effect was only 0.2% at 1 vol.% CO at 500 °C, which is close to the operating conditions of the MRF system. This study quantitatively revealed that the CO inhibition effect on hydrogen flux is extremely small when the membrane is operated at temperatures equal to or higher than 500 °C, even for state-of-the-art thin membranes. The performance of the Tokyo Gas MRF seems thus mainly limited by concentration polarization effects.