A micro-solid oxide fuel cell system as battery replacement

The concept and the design of a micro-solid oxide fuel cell system is described and discussed. The system in this study is called the ONEBAT system and consists of the fuel cell PEN (positive electrode – electrolyte – negative electrode) element, a gas processing unit, and a thermal system. PEN elements of free-standing multi-layer membranes are fabricated on Foturan^® and on Si substrates using thin film deposition and microfabrication techniques. Open circuit voltages of up to 1.06 V and power of 150 mW cm⁻² are achieved at 550 °C. The membranes are stable up to 600 °C. The gas processing unit allows butane conversion of 95% and hydrogen selectivity of 83% at 550 °C in the reformer and efficient after-burning of hydrogen, carbon monoxide, and lower hydrocarbons in the post-combustor. Thermal system simulations prove that a large thermal gradient of more than 500 °C between the hot module and its exterior are feasible. The correlation between electrical power output – system size and thermal conductivity – heat-transfer coefficient of the thermal insulation material are shown. The system design studies show that the single sub-systems can be integrated into a complete system and that the requirements for portable electronic devices can be achieved with a base unit of 2.5 W and a modular approach.     

Fluorescent Imaging of Extracellular Fungal Enzymes Bound onto Plant Cell Walls

Lignocelluloytic enzymes are industrially applied as biocatalysts for the deconstruction of recalcitrant plant biomass. To study their biocatalytic and physiological function, the assessment of their binding behavior and spatial distribution on lignocellulosic material is a crucial prerequisite. In this study, selected hydrolases and oxidoreductases from the white rot fungus Phanerochaete chrysosporium were localized on model substrates as well as poplar wood by confocal laser scanning microscopy. Two different detection approaches were investigated: direct tagging of the enzymes and tagging specific antibodies generated against the enzymes. Site-directed mutagenesis was employed to introduce a single surface-exposed cysteine residue for the maleimide site-specific conjugation. Specific polyclonal antibodies were produced against the enzymes and were labeled using N-hydroxysuccinimide (NHS) ester as a cross-linker. Both methods allowed the visualization of cell wall-bound enzymes but showed slightly different fluorescent yields. Using native poplar thin sections, we identified the innermost secondary cell wall layer as the preferential attack point for cellulose-degrading enzymes. Alkali pretreatment resulted in a partial delignification and promoted substrate accessibility and enzyme binding. The methods presented in this study are suitable for the visualization of enzymes during catalytic biomass degradation and can be further exploited for interaction studies of lignocellulolytic enzymes in biorefineries.     

160-Gb/s all-optical demultiplexing using a gain-transparentultrafast-nonlinear interferometer (GT-UNI)

We report on an all-optical demultiplexer based on gain-transparent operation of a semiconductor optical amplifier (SOA) in an ultrafast-nonlinear interferometer (GT-UNI). The GT-UNI comprises a robust fiber-chip setup in a folded geometry. For switching window widths of 5.2 ps and 6.0 ps, error-free demultiplexing of 160-10 Gb/s is demonstrated     

High Bit Rate OTDM-Transmission on Standard Fibre

In this paper we describe experimental and numerical studies on high bit rate, single span transmission system over a length of 160 km without amplifiers in the link (unrepeatered). From these studies we revealed that the tolerance of the residual dispersion is very restrictive. Proper dispersion management and PMD compensation techniques are important topics in these and future systems.     

Acidification of forested podzols in North Belgium during the period 1950-2000

Acidification of forest soils in Europe and North America has been an important concern over the last decades. The last area-covering survey of forest soil acidification in Flanders (North Belgium) goes back to 1985 [Ronse A, De Temmerman L, Guns M, De Borger R. Evolution of acidity, organic matter content, and CEC in uncultivated soils of North Belgium during the past 25 years. Soil Sci; 146, (1988), 453-460] and highlighted a significant acidification of the upper layer (0.3-0.4 m) of forested podzols during the period 1950-1985. The present study aimed to assess (1) to what extent further acidification of forested podzols occurred during the period 1985-2000 at different depths and (2) whether the average annual acidification rate accelerated or slowed down between 1985 and 2000 compared to the period 1950-1985. Average soil pH-KCl values of podzols in northern Belgium dropped during the period 1985-2000. This decline extends to a depth of about 50 cm but was most pronounced and significant in the A horizon. In the A(0), A(1) and A(2) horizons, average pH dropped with 0.2, 0.3 and 0.1 units, and in the B(ir) and C horizons with 0.1 units. No change in average pH value occurred in the B(h) horizon. Average annual acidification rate of the A(1) horizon was significantly higher in the period 1985-2000 than in the period 1950-1985. Changes in pH occurred in the entire soil profile during the period 1950/67-1985 likely because sulphate was the major form of acid deposition before 1985. After 1985, acid sulphur deposition decreased with more than 50% in North Belgium. In contrast, ammonium deposition almost doubled between 1950 and 1980, which may explain why soil acidification between 1985 and 2000 has been restricted to the upper soil horizons.     

工业4.0时代钢铁行业转型中的新型服务

伴随着数字化和工业4. 0的快速发展,出现了多种新型的冶金服务模式,并且这些服务模式与中国钢铁行业"十三五"规划制定的转型升级措施相吻合。用3个实例进一步验证了钢铁生产企业要想保持良好的竞争力,与拥有雄厚实力且能提供设备制造、工艺、电气自动化和全方位服务支持的原始设备供应商,建立长期合作、互利共赢的合作关系是十分必要性的。     

Exposure of engineered nanoparticles to human lung epithelial cells: influence of chemical composition and catalytic activity on oxidative stress

The chemical and catalytic activity of nanoparticles has strongly contributed to the current tremendous interest in engineered nanomaterials and often serves as a guiding principle for the design of functional materials. Since it has most recently become evident that such active materials can enter into cells or organisms, the present study investigates the level of intracellular oxidations after exposure to iron-, cobalt-, manganese-, and titania-containing silica nanoparticles and the corresponding pure oxides in vitro. The resulting oxidative stress was quantitatively measured as the release of reactive oxygen species (ROS). The use of thoroughly characterized nanoparticles of the same morphology, comparable size, shape, and degree of agglomeration allowed separation of physical (rate of particle uptake, agglomeration, sedimentation) and chemical effects (oxidations). Three sets of control experiments elucidated the role of nanoparticles as carriers for heavy metal uptake and excluded a potential interference of the biological assay with the nanomaterial. The present results indicate that the particles could efficiently enter the cells by a Trojan-horse type mechanism which provoked an up to eight times higher oxidative stress in the case of cobalt or manganese if compared to reference cultures exposed to aqueous solutions of the same metals. A systematic investigation on iron-containing nanoparticles as used in industrial fine chemical synthesis demonstrated that the presence of catalytic activity could strongly alter the damaging action of a nanomaterial. This indicates that a proactive development of nanomaterials and their risk assessment should consider chemical and catalytic properties of nanomaterials beyond a mere focus on physical properties such as size, shape, and degree of agglomeration.     

Cloning and characterization of RLPK, a novel RSK-related protein kinase

A novel protein kinase whose activity can be stimulated by mitogen in vivo was cloned and characterized. The cDNA of this gene encodes an 802-amino acid protein (termed RLPK) with the highest homology (37% identity) to the two protein kinase families, p90(RSK) and p70(RSK). Like p90(RSR), but not p70(RSK), RLPK also contains two complete nonidentical protein kinase domains. RLPK mRNA is widely expressed in all human tissues examined and is enriched in the brain, heart, and placenta. In HeLa cells, transiently expressed epitope-tagged RLPK can be strongly induced by epidermal growth factor, serum, and phorbol 12-myristate 13-acetate, but only moderately up-regulated by tumor necrosis factor-alpha and other stress-related stimuli. The activity of RLPK stimulated by epidermal growth factor was not inhibited by several known protein kinase C inhibitors nor by rapamycin, a known specific inhibitor for p70(RSK), but could be inhibited by herbimycin A, a tyrosine kinase inhibitor, and partially inhibited by PD98059 or SB203580, inhibitors for the mitogen-activated protein kinase pathways. Recombinant RLPK possesses high phosphorylation activity toward histone 2B and the S6 peptide, RRRLSSLRA. Although purified recombinant RLPK can be phosphorylated by ERK2 and p38alpha in vitro, its activity is not affected by this phosphorylation. Moreover, the treatment of RLPK with acid phosphatase did not reduce its in vitro kinase activity. These data suggest that RLPK is structurally similar to previously isolated RSKs, but its regulatory mechanism may be distinct from either p70(RSK) or p90(RSK)s.