On the relations between color,gloss, and surface texture in injection‐molded plastics

The relation between color and gloss of injection‐molded plastic specimens was evaluated by means of a 45°/0° geometry spectrophotometer and a glossmeter. The specimens were plaques having one smooth, glossy field and one rougher, textured region made of two different polymeric materials (acrylonitrile‐butadiene‐styrene and polypropylene) in a range of colors. A significant influence of the lightness L* of the specimens on the measured gloss of the textured field, with a low gloss appearance, was found. This can probably be attributed to a contribution from bulk scattering, which is linked to the reflectance from within the specimen. The influence of texture on the measured color of the plaques was assessed by evaluating the color difference between the smooth field and the more textured area on the specimens. When the surface was textured, the color changed; in general it became lighter and less saturated. The magnitude of the change depended on the color of the material. The darker the material was, the larger was the increase in lightness L* as the surface became rougher. The shift in chroma C* was determined not only by the saturation but also by the lightness of the specimens. Darker specimens exhibited a larger decrease in chroma when the surface was textured. The change in the measured color caused by increasing the surface roughness could be predicted in a satisfactory manner using a model developed for xerographic printing paper. © 2009 Wiley Periodicals, Inc. Col Res Appl, 34, 291–298, 2009     

Low‐Temperature Superionic Conductivity in Strained Yttria‐Stabilized Zirconia

Very high lateral ionic conductivities in epitaxial cubic yttria‐stabilized zirconia (YSZ) synthesized on single‐crystal SrTiO₃ and MgO substrates by reactive direct current magnetron sputtering are reported. Superionic conductivities (i.e., ionic conductivities of the order ～1 Ω^?1cm^?1) are observed at 500 °C for 58‐nm‐thick films on MgO. The results indicate a superposition of two parallel contributions – one due to bulk conductivity and one attributable to conduction along the film–substrate interface. Interfacial effects dominate the conductivity at low temperatures (<350 °C), showing more than three orders of magnitude enhancement compared to bulk YSZ. At higher temperatures, a more bulk‐like conductivity is observed. The films have a negligible grain‐boundary network, thus ruling out grain boundaries as a pathway for ionic conduction. The observed enhancement in lateral ionic conductivity is caused by a combination of misfit dislocation density and elastic strain in the interface. These very high ionic conductivities in the temperature range 150–500 °C are of great fundamental importance but may also be technologically relevant for low‐temperature applications.     

Inhibition of Human DHODH by 4‐Hydroxycoumarins,Fenamic Acids,and N‐(Alkylcarbonyl)anthranilic Acids Identified by Structure‐Guided Fragment Selection

A strategy that combines virtual screening and structure‐guided selection of fragments was used to identify three unexplored classes of human DHODH inhibitor compounds: 4‐hydroxycoumarins, fenamic acids, and N‐(alkylcarbonyl)anthranilic acids. Structure‐guided selection of fragments targeting the inner subsite of the DHODH ubiquinone binding site made these findings possible with screening of fewer than 300 fragments in a DHODH assay. Fragments from the three inhibitor classes identified were subsequently chemically expanded to target an additional subsite of hydrophobic character. All three classes were found to exhibit distinct structure–activity relationships upon expansion. The novel N‐(alkylcarbonyl)anthranilic acid class shows the most promising potency against human DHODH, with IC₅₀ values in the low nanomolar range. The structure of human DHODH in complex with an inhibitor of this class is presented.     

Fe(O)/lignitic coal: an efficient and mechanically stable reactive material for purification of water containing heavy metals, radionuclides, and nitroaromatics

Mine water in the former uranium mine of K?nigstein (Saxony, Germany) contains high concentrations of acid, sulfate, iron, aluminum, various heavy metals, radionuclides, and nitroaromatics. Research has been conducted for several years to establish the extent to which reduction of pollutant concentrations can be positively influenced and accelerated by storage of reactive materials in mine cavities. Investigations were made at different scales to test and select materials with respect to maximum fixation of contaminants (underground column tests) to examine hydraulic effects (underground large-scale column tests) and to optimize material properties (laboratory tests). The investigations have shown that a mixture of Fe chips and lignitic coal is capable of efficiently cleaning acid and contaminant-containing mine water. The examined material is easily available and compatible with the environment. A large-scale application of such a reactive barrier is being considered for mine water treatment in the future and is deemed to be a reasonable conception for a safety component after conclusion of the flooding.     

In Situ Mine Water Treatment: Field Experiment at the Flooded Königstein Uranium Mine (Germany)

Within the WISMUT environmental remediation programme, the rehabilitation of the former uranium mine at Königstein is a very special case due to its use of underground leaching and its location near the Elbe River. The mine water is acidic, oxidizing, and polluted with uranium and other contaminants, and must be pumped to the surface and treated. In-situ water treatment approaches have been investigated to optimise further flooding and shorten the period of conventional water treatment. In 2010/2011, a field-scale experiment was carried out: about 120 t of alkalinity were successfully injected into the partially flooded mine. Tracer signals and geochemical reactions achieved general expectations. Based on the results, a site-specific technology concept was developed to flood the mine to its natural decant level.     

Supplier credits, limited liquidity, and timely demand information

We consider supplier-credit contracting between a manufacturer and a liquidity-constrained dealer. We show that the timeliness according to which the dealer receives demand information has a significant impact on the optimal contract. If the manufacturer cannot be sure that a dealer without liquidity has demand information when the contract is written, the optimal contract assigns the same quantity to an ignorant dealer and a dealer who knows that there are unfavorable demand conditions. However, dealers with favorable demand information are screened. If the dealer??s liquidity rises, the manufacturer proposes a contract that resembles the solution of a classic adverse selection model in the spirit of Harris et?al. (Manag Sci 28:604?C620, 1982). For high liquidity, the optimal supplier-credit contract assigns the same quantity to an ignorant dealer and dealers who have favorable demand information whereas dealers with unfavorable demand information are screened.     

Food-web structure in low- and high-dimensional trophic niche spaces

A question central to modelling and, ultimately, managing food webs concerns the dimensionality of trophic niche space, that is, the number of independent traits relevant for determining consumer–resource links. Food-web topologies can often be interpreted by assuming resource traits to be specified by points along a line and each consumer''s diet to be given by resources contained in an interval on this line. This phenomenon, called intervality, has been known for 30 years and is widely acknowledged to indicate that trophic niche space is close to one-dimensional. We show that the degrees of intervality observed in nature can be reproduced in arbitrary-dimensional trophic niche spaces, provided that the processes of evolutionary diversification and adaptation are taken into account. Contrary to expectations, intervality is least pronounced at intermediate dimensions and steadily improves towards lower- and higher-dimensional trophic niche spaces.     

The nature of the photochromism arising in the nanosized MoO3 films

We carried out the experiments which show unambiguously that not one, as it was commonly accepted, but three optical absorption bands corresponding to different color centers arise in the nanosized MoO₃ films due to hydrogen atoms. Varying the conditions for the photoinjection of hydrogen into the MoO₃ films, it is possible to change drastically the correlation between the concentrations of different arising centers, which in turn yields the great difference in the optical absorption spectra. Our findings are crucial for understanding of the nature of electrochromism and photochromism not only in MoO₃ films but also in the series of the transition metal oxide films.     

Principal Component Analysis of the Hydroxymethylation of Sugarcane Lignin: A Time-Depending Study by FTIR

Abstract

The hydroxymethylation of Acetosolv lignin from sugarcane bagasse was studied at 40°C between 0.25 and 8 h by Fourier-transformed infrared spectroscopy (FTIR). Principal Component Analysis (PCA) of the spectra has determined that addition of formaldehyde to the lignin fragments was completed within 4 h. After that time, only condensation of the fragments occurs, leading to a resol-type crosslinked resin. PCA performed in selected regions of the FTIR spectra showed that the same results are also obtained for the stretching region of O-H and C-H within the range from 2800 to 3800 cm^?1, which is not usually considered in the spectroscopic evaluations of modified lignins.