Interfacial shear strength of C/C composites

Fiber-bundle push-out, single-fiber push-in, and single-fiber push-out tests were conducted in order to examine the applicability of these methods for determining the interfacial shear strength of carbon-carbon composites. The fiber-bundle push-out test resulted mostly in fractures along the fiber/matrix interface but created a small amount of fractures in the matrix. Hence, the evaluated strength was regarded as an approximate value. In order to precisely evaluate the interfacial strength, push-in and push-out tests for a single fiber were performed using a micro-Vickers indentation tester. In these tests, the load has to be placed within a target fiber, and the indentation should not extend to the matrix. This condition restricted the load that could be applied to a carbon fiber. Within this limit, a single carbon fiber could not be pushed-in. For the sake of load reduction, single-fiber push-out tests were conducted using thin specimens. The thickness appropriate for a single-fiber push-out specimen was estimated based on the interfacial shear strength obtained by the bundle push-out tests. Below this thickness, single-fiber push-out tests could be successfully performed.     

Our current understanding of lake ecosystem response to climate change: What have we really learned from the north temperate deep lakes?

Climatic change is recognized as an important factor capable of influencing the structural properties of aquatic ecosystems. Lake ecosystems are particularly sensitive to climate change. Several long time-series studies have shown close coupling between climate, lake thermal properties and individual organism physiology, population abundance, community structure, and food-web structure. Understanding the complex interplay between climate, hydrological variability, and ecosystem structure and functioning is essential to inform water resources risk assessment and fisheries management. The purpose of this paper is to present the current understanding of climate-induced changes on lake ecosystem phenology. We first review the ability of climate to modulate the interactions among lake hydrodynamics, chemical factors, and food-web structure in several north temperate deep lakes (e.g., Lake Washington, Lake Tahoe, Lake Constance, Lake Geneva, Lake Baikal, and Lake Zurich). Our aim is to assess long-term trends in the physical (e.g., temperature, timing of stratification, and duration of ice cover), chemical (e.g., nutrient concentrations), and biological (e.g., timing of the spring bloom, phytoplankton composition, and zooplankton abundance) characteristics of the lakes and to examine the signature of local weather conditions (e.g., air temperature and rainfall) and large-scale climatic variability (e.g., ENSO and PDO) on the lake physics, chemistry and biology. We also conducted modeling experiments to quantify the relative effect of climate change and nutrient loading on lake phenology. These modeling experiments focused on the relative changes to the major causal associations underlying plankton dynamics during the spring bloom and the summer stratified period. To further understand the importance of climate change on lakes, we propose two complementary directions of future research. First, additional research is needed to elucidate the wide array of in-lake processes that are likely to be affected by the climate change. Second, it is essential to examine the heterogeneity in responses among different water bodies. The rationale of this approach and its significance for dealing with the uncertainty that the climate signals cascade through lake ecosystems and shape abiotic variability and/or biotic responses have been recently advocated by several other synthesis papers.     

New method for testing phototoxicity of polycyclic aromatic hydrocarbons

Polycyclic aromatic hydrocarbons (PAHs), widespread environmental pollutants, were recently reported to show photomutagenesis. As contaminants in the environment are usually exposed to sunlight, a way to evaluate the phototoxic characteristics of pollutants is required. We have previously found that phosphorylation of histone H2AX (gamma-H2AX), which accompanied the induction of DNA double strand breaks (DSBs), was significantly induced by low concentrations of benzo[a]pyrene (10(-9)-10(-7) M) and UVA (0.6 J/cm2) in CHO-K1 cells. Higher concentrations have been required for the detection of DSBs. The aim of the present study is to investigate the applicability of gamma-H2AX in a new phototoxicity assay of PAHs. The human keratinocytes, HaCaT, were treated with four model PAHs (naphthalene, phenanthrene, pyrene, and benzo[a]pyrene, 10(-11)-10(-7) M) and/or UVA (5 J/cm2), and the induction of gamma-H2AX was assessed. Furthermore, DSBs were directly detected using a biased sinusoidal field gel electrophoresis, and the cell viability was examined as a general assay of phototoxicity. The induction of gamma-H2AX was detected in the presence of all the PAHs except naphthalene at concentrations of 10(-9)-10(-7) M, whereas neither DSBs nor cell death could be detected at those concentrations, and higher concentrations were required for the detection. Naphthalene showed no phototoxicity in any of the three different assays. These findings suggest that histone H2AX is a potential moleculartargetfor detecting the phototoxicity of PAHs more sensitively than the detection of cell viability and DSBs.     

Significance of the detection of staphylococcal enterotoxin A gene in low fat milk which caused a serious outbreak of food poisoning

In June 2000, there was a large-scale outbreak of food poisoning after consumption of Snow Brand low fat milk. In the evening of a day the incident made public, some cartons of low fat milk were brought to our laboratory for examination. Next day, we detected only staphylococcal enterotoxin (SE) A gene among SE (A-E) genes by PCR in left-over milk samples or samples from the same lots that patients had consumed. We presumed that the outbreak was caused by the intake of SEA. We subsequently confirmed the presence of SEA in these samples. To investigate the existence of SE (A-E) genes in milk, we examined 100 samples of commercial low fat milk and milk by PCR, but none of the genes was detected. We estimated the detection limit of SEA gene in low fat milk by PCR. Four strains of SEA-producing Staphylococcus aureus cultures were serially diluted in low fat milk. The SEA gene was detected at levels of 5.5 x 10(2) to 1.6 x 10(4) cfu/mL of S. aureus. These amounts of S. aureus are higher than the values in raw milk reported previously. Therefore we consider that SE genes in low fat milk should usually be undetectable by our PCR. This study shows that quick detection of SE genes by PCR is very helpful to analyze outbreaks, especially if no significant bacterium can be cultured.     

Hydration behavior of perfluorinated and hydrocarbon-type proton exchange membranes: Relationship between morphology and proton conduction

The relationships between morphology and proton conduction for Nafion membranes and hydrocarbon-type proton exchange membranes, namely, sulfonated poly(arylene ether ether ketone) (S-PEEK) and sulfonated poly(arylene ether sulfone) (S-PES), were investigated by small-angle X-ray scattering (SAXS) and atomic force microscopy (AFM). The direct simultaneous observation of surface morphology and active regions of proton conduction on membranes by combined high-resolution AFM phase imaging and an electrochemical technique at controlled humidity provided significant morphological information, particularly for the hydrocarbon-type membranes that exhibit few or no features on SAXS profiles. For the Nafion membranes, the active proton paths became denser and congregated with each other at over 60% RH, resulting in the formation of well-connected networks. For the hydrocarbon-type membranes, however, only the relatively small and dispersed proton paths were observed, which showed no significant change even as water content increased. We have demonstrated that the differences in microscopic morphology between the Nafion and hydrocarbon-type membranes are associated with the differences between their macroscopic proton conductivities.     

Effects of sample orientation on nonpiloted ignition of thin poly(methyl methacrylate) sheets by a laser: 2. Experimental results

The effect of the sample orientation angle on frontside (irradiated surface) ignition and subsequent backside (nonirradiated surface) flame appearance over thin poly(methyl methacrylate) (PMMA) sheets having thicknesses of 0.2 and 0.5 mm has been experimentally investigated, using a CO₂ laser as an external radiant source in quiescent normal gravity. The sample orientation angle was varied from θ=−90° (ceiling configuration) to +90° (floor configuration) at intervals of 15° under three different laser powers of 16.0, 17.3, and 26.1 W. The shortest frontside ignition delay time was observed for the ceiling configuration (θ=−90°) and frontside ignition delay time significantly varied with increase in sample orientation angle at a laser power of 16.0 W. As the laser power was increased, frontside ignition was observed at all angles and its delay time became less dependent on the sample orientation angle. The appearance of a backside flame was achieved after the formation of an open hole (due to local consumption of the sample) by two different processes: the onset of laser induced ignition over the backside sample (backside ignition) and a flame traveling from the frontside through an open hole to the backside (backside flame). The former process was observed for a limited number of cases only around the vertical configurations (−30°?θ?30°). The delay time for the appearance of backside flame tended to be longer for sample surfaces facing downward (θ°<0) than for the sample surface facing upward (θ?0°) regardless of the laser power. When the duration of laser irradiation was shortened from 10 to 4 s, as soon as the laser was shut off, the flame on the frontside immediately shrank, moved close to the sample surface, and then traveled rapidly to the backside. Therefore, the delay time of backside flame appearance (about 6 s) became longer with longer duration of laser irradiation after the onset of a frontside flame. The size of the hole (about 4 mm diameter) was large enough for the flame to travel through it, even after 4 s of laser irradiation to sample. These results indicate that the size of the hole appears to be not a critical parameter for the appearance of the backside flame.     

Nanotrap and mass analysis of aromatic molecules by phenyl group-modified nanoparticle

To functionalize the surface of nanoparticles with phenyl groups for subsequent cross-linking with aromatic molecules by mutual interactions, we prepared functional nanoparticles (d = 3 nm) by silanization with phenyl-triethoxysilane. The nanoparticles had Fe(2)O(3) cores conjugated to phenyl groups; this was confirmed by Fourier transform infrared (FT-IR) spectroscopy and absorption spectrophotometry. The typical C-H and C-C peaks and the absorption at 240 nm, which corresponds to aromatic rings, were detected in the spectroscopic results for the phenyl group-modified nanoparticles. The nanoparticles could ionize aromatic (colchicine, reserpine, and bradykinin peptide) and nonaromatic (L-α-phosphatidylethanolamine,dioleoyl, and polyethylene glycol) molecules by nanoparticle-assisted laser desorption/ionization mass spectrometry. The nanoparticles worked as a selective trap and an ionization-assisting reagent in mass spectrometry for the aromatic molecular targets.     

The citation system: Citation networks as repeatedly focusing on difference, continuous re-evaluation, and as persistent knowledge accumulation

It can be shown that claims of a lack of theories of citation are also indicative of a grate need for a theory which links science dynamics and measurement. There is a wide gap between qualitative (science dynamics) and quantitative (measurement) approaches. To link them, the present study proposes the use of the citation system, that potentially bridges a gap between measurement and epistemology, by applying system theory to the publication system.     

Network structures and dynamics of dry and swollen poly(acrylate)s. Characterization of high- and low-frequency motions as revealed by suppressed or recovered intensities (SRI) analysis of C NMR

We recorded temperature-dependent high-resolution ¹³C NMR spectra of dry and swollen poly(acrylate)s [poly(2-methoxyethyl acrylate) (PMEA), poly(2-hydroxyethyl methacrylate) (PHEMA), and poly(tetrahydrofurfuryl acrylate) (PTHFA)] by dipolar decoupled-magic angle spinning (DD-MAS) and cross-polarization-magic angle spinning (CP-MAS) methods, to gain insight into their network structures and dynamics. Suppressed or recovered intensities (SRI) analysis of ¹³C CP-MAS and DD-MAS NMR was successfully utilized, to reveal portions of dry and swollen polymers which undergo fast and slow motions with fluctuation frequencies in the order of 10⁸ Hz and 10⁴-10⁵ Hz, respectively. Fast isotropic motions with frequency higher than 10⁸ Hz at ambient temperature were located to the portions in which ¹³C CP-MAS NMR signals of swollen PMEA were selectively suppressed. In contrast, low-frequency motion was identified to the portions in which ¹³C DD-MAS (and CP-MAS) signals are most suppressed at the characteristic suppression temperature(s) T_s. Network of PMEA gels (containing 7 wt% of water) turns out to be formed by partial association of backbones only, as manifested from their T_s gradient at lowered temperature, whereas networks of PHEMA (containing 40 wt% of water) and PTHFA (9 wt% of water) gels are tightly formed through mutual inter-chain associations of both backbones and side-chains, as viewed from the raised T_s values for both near at ambient temperature. It is also interesting to note that flexibility of gel network (PMEA > PTHFA > PHEMA) characterized by the suppression temperature T_s (PMEA < PTHFA < PHEMA) is well related with a characteristic parameter for biocompatibility such as the production of TAT (thrombin-antithrombin III complex) as a marker of activation of the coagulation system.