Heterogeneity in Formation of Lignin. XIII. Formation of p-Hydroxyphenyl Lignin in Various Hardwoods Visualized by Microautoradiography

The heterogeneous nature of hardwood lignin was shown by visualizing the deposition process of p-hydroxyphenyl (H) lignin in the differentiating xylem of magnolia, beech, lilac and poplar. When p-glucocoumaryl alcohol-[arom. ring-2-³H], an efficient precursor of H units in lignin, was administered to the differentiating xylem of these trees, radioactivity was incorporated in the compound middle lamella region of vessel and fiber cell walls. The deposition of H units occurs only in the early stage of cell wall formation when the outer layer of the secondary wall is formed. H lignin deposits mainly within pectic substances and hemicellulose gel to form a highly condensed structural moiety.     

Dendrite growth processes of silicon and germanium from highly undercooled melts

The crystal growth behavior of a semiconductor from a very highly undercooled melt is expected to be different from that of a metal. In the present experiment, highly pure undoped Si and Ge were undercooled by an electromagnetic levitation method, and their crystal growth velocities (V) were measured as a function of undercooling (ΔT). The value of V increased with ΔT, and V=26 m/s was observed at ΔT=260 K for Si. This result corresponds well with the predicted value based on the dendrite growth theory. The growth behaviors of Si and Ge were found to be thermally controlled in the measured range of undercooling. The microstructures of samples solidified from undercooled liquid were investigated, and the amount of dendrites immediately after recalescence increased with undercooling. The dendrite growth was also observed by a high-speed camera.     

Nondaily behavior detection monitoring system for elderly people based on bayesian network representation of omnidirectional vision sensor

This paper describes an unusual behavior detection system based on an omnidirectional vision sensor, as one of the important elements in realizing “Sensing and Robotic Support Rooms” for elderly people. Such support rooms are expected to be further developed in the future with advanced abilities to automatically recognize elderly people's actions and behavior patterns, to detect unusual patterns by using sensors, and to support their daily motions by using robotic manipulator control systems. The proposed monitoring system using an omnidirectional vision sensor automatically learns daily behavior patterns and detects unusual behavior patterns and actions by using the Bayesian network approach. The Bayesian network is constructed by using image feature values such as area and center‐of‐gravity values extracted from a captured image sequence, and the respective behavior patterns are represented as conditional probabilities. Unusual behavior patterns can be automatically detected on the basis of the low generation probability values. Experiments based on the investigation of elderly people's typical daily behavior patterns have shown the effectiveness of the proposed system. © 2010 Wiley Periodicals, Inc. Electr Eng Jpn, 172(3): 42–51, 2010; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/eej.20990     

Energy-level alignment at model interfaces of organic electroluminescent devices studied by UV photoemission: trend in the deviation from the traditional way of estimating the interfacial electronic structures

The electronic structures of model interfaces of organic electroluminescent (EL) devices were investigated with UV photoemission spectroscopy (UPS). Interfaces of TTN (tetrathianaphthacene) and TCNQ (tetracyanoquinodimethane) were also studied as extreme cases for hole transport and electron transport material, respectively. For all organic/metal interfaces studied, the work function of metal electrode was changed by deposition of organic layer, i.e., the vacuum level was shifted at the interface, indicating the invalidity of the traditional energy level alignment model where a common vacuum level was assumed at organic/metal interface. At TCNQ/Au, DP-NTCI/Al, which are acceptor/metal interfaces, upward shift of the vacuum level of organic layer relative to that of metal was observed, suggesting the formation of interfacial dipole due to electron-transfer from metal to acceptor. At other organic/metal interfaces, TPD(N, N'-diphenyl-N, N'-(3-methylphenyl)-1, 1'-biphenyl-4, 4'-diamine)/Au or ITO (indium tin oxide), ALq/sub 3/ (tris(8-hydroxyquinolino) aluminum)/Al, DP-NTCl(N, N'-diphenyl-1,4,5,8- naphthyltetracarboxylimide)/Al or Au, downward shift of the vacuum level was observed. Such downward shift has been also observed in our previous study for porphyrin/metal interfaces, and seems to be a trend for organic/metal interfaces at which no electron-transfer from metal to organic layer occurs. This trend suggests that the traditional model tends to underestimate (overestimate) the barrier height for hole (electron) injection. On the other hand, the vacuum level shift at ALq/sub 3//TPD interface was less than 0.1 eV, leading to an apparent applicability of the traditional model. However, it is not always the case for organic/organic interfaces: finite shift of 0.2 eV was observed at TTN/TCNQ interface due to electron-transfer from TTN to TCNQ. Possible origins of vacuum level shift at organic/metal interfaces were also discussed.     

The Chemistry of PCR Primers: Concept and Application

DNA is a typical organic compound with marked differences from other chemicals and biopolymers because DNA can be amplified by the enzyme polymerase. DNA can be, in principle, amplified from a single copy by the polymerase chain reaction (PCR). In this review, we focus our attention on the chemistry of PCR primers. Because PCR is basic technology in biology research fields, we sometimes use chemically labeled primers without any awareness of the chemistry they leave behind. We would like to emphasize that chemically labeled primers contain a lot of potential for different chemistry ideas and much study is still necessary to advance PCR for single-nucleotide polymorphism (SNP) typing, genetic diagnosis, and other fields. Two categories of primers, affinity-capture primers and signaling primers, are discussed from the viewpoints of their chemical concepts and applications. Affinity-capture primers are used for purification, isolation, and manipulation of PCR products by high specificity and affinity to the cognate molecules by molecule molecule interactions, whereas signaling primers report the hybridization and/or progress of PCR amplification by a signal change, in most cases by a fluorescence change. The content of this review may be useful for a better understanding of the chemistry of PCR primers and, more importantly, for the invention of novel PCR chemistry.     

Analysis of proton exchange membrane fuel cell catalyst layers for reduction of platinum loading at Nissan

The biggest issue that must be addressed in promoting widespread use of fuel cell vehicles (FCVs) is to reduce the cost of the fuel cell system. Especially, it is of vital importance to reduce platinum (Pt) loading of catalyst layers (CLs) in the membrane electrode assembly (MEA) of a proton exchange membrane fuel cell (PEMFC). In order to lower the Pt loading of the MEA, mass transport of reactants related to the performance in high current density should be enhanced significantly as well as kinetics of the catalyst, which can result in the better Pt utilization and effectiveness. In this study, we summarized our analytical approach and methods for reduction of Pt loading in CLs. Microstructure, mass transport properties of the reactants, and their relation in CLs were elucidated by applying experimental analyses and computational methods. A simple CL model for I–V performance prediction was then established, where experimentally elucidated parameters of the microstructure and the properties in CLs were taken into account. Finally, we revealed the impact of lowering the Pt loading on the transport properties, polarization, and the I–V performance.     

Electrolyte properties of 1-alkyl-2,3,5-trimethylpyrazolium cation-based room-temperature ionic liquids for lithium secondary batteries

The physicochemical and electrochemical properties of three 1-alkyl-2,3,5-trimethylpyrazolium cation-based room-temperature ionic liquids with various alkyl chain lengths were investigated. The temperature dependences of density, viscosity, and ionic conductivity were obtained by precise measurements. Electrolyte properties of these room-temperature ionic liquids were also examined from the viewpoint of their uses in lithium secondary batteries ([LiCoO₂ positive electrode|electrolyte|lithium metal negative electrode]). It was found that the alkyl chain length affects the charge–discharge performances of cells.     

Programmed High‐Hole‐Mobility Supramolecular Polymers from Disk‐Shaped Molecules

In this paper a simple, casting solution technique for the preparation of two‐dimensional (2D) arrays of very‐high molecular weight (MW) 1D‐Pc supramolecular inorganic polymers is described. The soluble fluoroaluminium tetra‐tert‐butylphthalocyanine (ttbPcAlF) is synthesized and characterized, which can be self‐assembled to form 2D arrays of very‐high‐MW 1D‐Pc supramolecular inorganic polymers. High‐resolution transmission electron microscopy (HRTEM) demonstrates that the 1D‐ttbPcAlF, having a cofacial ring spacing of ～0.36 nm and an interchain distance of ～1.7 nm, self‐assembles into 2D‐nanosheets (～140 nm in length, ～20 nm in width, and equivalent to MW of 3.2 × 10⁵ g mol^?1). The film cast from a 1,2‐dichloroethane (DCE) solution shows a minimum hole‐mobility of ～0.3 cm² V^?1 s^?1 at room temperature by flash‐photolysis time‐resolved microwave conductivity (TRMC) measurements and a fairly high dark dc‐conductivity of ～1 × 10^?3 S cm^?1.     

Superstructure-based design and operation for biomass utilization networks

This paper is providing a design and evaluation methodology for biomass utilization networks (B-NETs) planning in local areas. The methodology is an effort to integrate various exertions of many researchers as well as stakeholders in the biomass field including process technologies, local area classification and renewable energy mechanisms to design and evaluate B-NETs. The proposed design methodology has three steps: classification, problem formulation and suggesting solution methods. The core part of planning the B-NETs utilization methodology is the superstructure that is a super class model for the processes of biomass utilization networks that has to be built for the local area. The biomass utilization superstructure (BUSS) relates the biomass resources to their products, available processes, and possible future processes of utilization in static manner. Although the local area BUSS is static in nature, it shows the decision makers what kinds of B-NETs are, or can be, available in their area. It is important to note that for each super class process there exists a number of elemental technologies, or what we call unit process (UP), that can perform the job under the same condition with different processing constraint. To support the design and operation process a technological information infrastructure (TII) needs to be built to work as an information pool and simulation tool. With the support of TII and the BUSS different scenarios can be synthesized, analyzed and compared. Scenarios development enables the designer to check processing alternatives as well as biomass promotion mechanisms that fit the concerns of various stakeholders. The results of the methodology application can be given in the form of suggestions of a specific network class(es) or scenarios that can be applied in a class of localities with the same characteristics. Following to methodology configuration, a proposal for optimization methods is discussed and a case study for comparing biomass network scenarios in mountainous city is introduced.