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141.
Frantiek Hrabk Jan Lokaj Martin Tkaczyk Elena Morozova Valentina Eliseeva Leonid Chuiko Gennadii Voloshin 《大分子材料与工程》1986,144(1):219-227
A technical dye of the anthraquinone type was analyzed by GPC, mass spectroscopy, and elemental analysis. Along with the polymerizable component, N-[4-amino-3-methoxyanthraquinonyl-(1)] methacrylamide (I), it contained a saturated admixture, N-[4-amino-3-methoxyanthraquinonyl-(1)]-2-chloro-2-methylpropionamide (II). The homopolymerization of I was carried out, and admixture II was isolated and characterized. The copolymerization of the dye with styrene and methyl methacrylate was verified, and the retardation effect of II on the polymerization of these monomers was evaluated. 相似文献
142.
Benedikt Ley Corinna Ogonowski Jan Hess Tim Reichling Lin Wan Volker Wulf 《Behaviour & Information Technology》2014,33(8):815-828
Technological infrastructure at home is changing continuously and is becoming increasingly interconnected. Media devices, including the TV set, provide access to the Internet and offer manifold opportunities to consume media on demand. Additionally, personal devices, such as smartphones, also enable flexible consumption and sharing of media. Questions about how these technologies change the user's media usage and how these changes affect the social structure of a household, however, remain largely unanswered. In order to gain insight into the adoption of new technologies into daily routines, we explored these changes in respect of people's media usage in a qualitative long-term Living Lab study. We will present findings regarding personal routines, flexible integration of new devices into existing practices, influences on households as social systems and related issues in device access and collective use. We will highlight potentials and conflicts regarding device shifts and roles; restrictions in device access; social influences in the living room; and individual changes in media consumption. 相似文献
143.
In this paper we present a novel approach to simulate image formation for a wide range of real world lenses in the Monte Carlo ray tracing framework. Our approach sidesteps the overhead of tracing rays through a system of lenses and requires no tabulation. To this end we first improve the precision of polynomial optics to closely match ground‐truth ray tracing. Second, we show how the Jacobian of the optical system enables efficient importance sampling, which is crucial for difficult paths such as sampling the aperture which is hidden behind lenses on both sides. Our results show that this yields converged images significantly faster than previous methods and accurately renders complex lens systems with negligible overhead compared to simple models, e.g. the thin lens model. We demonstrate the practicality of our method by incorporating it into a bidirectional path tracing framework and show how it can provide information needed for sophisticated light transport algorithms. 相似文献
144.
Carsten Dachsbacher Jaroslav Křivánek Miloš Hašan Adam Arbree Bruce Walter Jan Novák 《Computer Graphics Forum》2014,33(1):88-104
Recent years have seen increasing attention and significant progress in many‐light rendering, a class of methods for efficient computation of global illumination. The many‐light formulation offers a unified mathematical framework for the problem reducing the full lighting transport simulation to the calculation of the direct illumination from many virtual light sources. These methods are unrivaled in their scalability: they are able to produce plausible images in a fraction of a second but also converge to the full solution over time. In this state‐of‐the‐art report, we give an easy‐to‐follow, introductory tutorial of the many‐light theory; provide a comprehensive, unified survey of the topic with a comparison of the main algorithms; discuss limitations regarding materials and light transport phenomena and present a vision to motivate and guide future research. We will cover both the fundamental concepts as well as improvements, extensions and applications of many‐light rendering. 相似文献
145.
Interactive rigid body simulation is an important part of many modern computer tools, which no authoring tool nor game engine can do without. Such high‐performance computer tools open up new possibilities for changing how designers, engineers, modelers and animators work with their design problems. This paper is a self contained state‐of‐the‐art report on the physics, the models, the numerical methods and the algorithms used in interactive rigid body simulation all of which have evolved and matured over the past 20 years. Furthermore, the paper communicates the mathematical and theoretical details in a pedagogical manner. This paper is not only a stake in the sand on what has been done, it also seeks to give the reader deeper insights to help guide their future research. 相似文献
146.
Attila Bereck Silke Dillbohner Burkhard Weber Dieter Riegel Jrg Mosel Johannes Michael Reper Axel Brakelmann 《Coloration Technology》1997,113(11):322-326
A simple method for the characterisation of fabric softness using a conventional tensile tester and a special measurement device has been developed. The method is demonstrated to be especially useful in detecting changes in softness of a given substrate due to different treatments. The results obtained, particularly hysteresis at 75% of the maximum extension, provide a good correlation with subjective ranking for samples that are subjectively distinguishable; they also differentiate well between samples which seem subjectively indistinguishable. Screening tests were carried out, mainly on wool fabrics, to find the effect of different treatments such as oxidative (alkaline and acidic) and reductive (Blankit IN) bleaching, dyeing with acid and a 1:2 metal complex, chrome and (mono and bi)reactive dyes, the effect of the antisetting agent Basolan AS (BASF) and of crosslinking with Irgasol HTW (CGY) on fabric softness. 相似文献
147.
Nucleating activity of the quinacridone and phthalocyanine pigments in polypropylene crystallization
Jan Broda 《应用聚合物科学杂志》2003,90(14):3957-3964
The nucleating ability of two organic pigments, quinacridone and phthalocyanine, in nonisothermal polypropylene (PP) crystallization was investigated. The investigations were carried out using DSC and polarizing microscopy. The efficiency of pigments in the nucleation process was determined in a simple test comparing the crystallization temperature of the PP‐containing pigments with respect to the pure polymer. Both pigments revealed good nucleating activity. In the presence of pigments the increment of the crystallization temperature and the increase of nucleation rate were observed. The nucleating efficiency of pigments was confirmed in investigations of the obtained structure. The nucleating activity of pigments was explained by their features fulfilling several requirements for good nucleating agents. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 3957–3964, 2003 相似文献
148.
Results of calculations based on a linearized multicomponent mass transfer theory developed by Burghardt and Krupiczka are compared with experimental data of Modine for condensation-evaporation process in ternary systems. These data have been obtained for acetone-benzene-nitrogen and acetone-benzene-helium in a welted wall column. Models I and II, which take into account diffusional interactions of components in a mullicomponent mixture show good agreement with the experiments as well as with other calculation methods (Krishna-Standart and Toor-Stewart-Prober). When multicomponent mass transfer occurs in the presence of inert species, a straightforward Model II is recommended. Model I, which is more universal, requires some iterative calculations with respect to the sum of mass fluxes. According to theoretical considerations the latter model is limited to the case of low total mass flux. The results of calculations for the systems studied were reasonably good though the total mass fluxes were not small. The calculation procedure based on the presented linearized models are convergent to the proper solutions in contrast to the Krishna-Standart Model IV which in some cases can be unstable. 相似文献
149.
Francisco Salmerón-Miranda Birgitta Båth Henrik Eckersten Johannes Forkman Maria Wivstad 《Nutrient Cycling in Agroecosystems》2007,79(2):125-139
The main objective of this field study was to estimate the total plant uptake of soil mineral N in maize (Zea mays L.) and common bean (Phaseolus vulgaris L.) grown in crop rotations under different N content in Nicaragua. Secondary objectives were to estimate the fraction of
the measured soil mineral N content taken up in this way, and to determine how the measured N in plant aboveground parts was
related to the total mineral N uptake. A large variation in N content was obtained by using data from fertilisation experiments.
Plant total N uptake was estimated as the residual N in a mass balance calculation of soil mineral N. Mineral N content in
the top 0–0.3 m soil layer in the field cultivations and in tubes isolated from root uptake, and N content in aboveground
plant parts were measured every 30 days. Estimated plant total uptake of soil mineral N varied considerably (2.5–14 g N m−2 30 day−1) over periods and N treatments. The range of variation was similar for maize and bean. The fraction of the soil mineral N
that was taken up by the plant daily varied more in maize (about 0.03–0.12 day−1) than in bean (about 0.05–0.08 day−1). Our results suggest that monthly changes in N in aboveground plant parts were linearly related to plant total N uptake
during the same period. Aboveground plant N constituted between about 55% and 80% of total uptake of soil mineral N in maize
depending on period within season, whereas for bean it was more constant and smaller (about 40%). 相似文献
150.
Julian Chojnowski Slawomir Rubinsztajn Witold Fortuniak Jan Kurjata 《Journal of Inorganic and Organometallic Polymers and Materials》2007,17(1):173-187
Summary Reactions of hexamethylcyclotrisiloxane, D3, with 1,1,3,3-tetramethyldisiloxane, HMMH, 1,1,1,3,3-pentamethyldisiloxane, HMM, phenyldimethylsilane and phenylmethylsilane catalyzed by tris(pentafluorophenyl)borane were studied. These reactions lead
to ring opening of D3 by the SiH reactant producing open chain oligomers with hydrosilane functionality at one or both chain ends. The reactivity
of the hydrosilanes toward D3 decreases in the series: PhMeSiH2 > HMMH > PhMe2SiH > HMM. Competitive self-oligomerization of HMMH and HMM also occurs. Primary products of these processes are able to enter into reactions with the SiH and D3 reactants; some also undergo cyclization. Thus, consecutive and competitive processes lead to a series of various oligohomologues.
Gas chromatography in conjunction with chemical ionization mass spectroscopy permitted identification of structure and determination
of the basic directions of these oligomerization processes. Polysiloxanes of higher molecular weight may be also formed in
some of these systems. The reactions, which occur in the systems studied, are rationalized on the basis of the mechanism involving
the hydride transfer from silicon to trivalent boron. This includes the transient formation of tertiary trisilyloxonium borate
which decomposes by the hydride transfer to one of the silicon atoms of the trisilyloxonium center.
Footnote: This paper is dedicated to Professor Ian Manners in recognition of his significant contributions to the field of
organometallic polymers. 相似文献