248 research outputs found

    Note on the Preparation of Some Thiobarbiturates

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    It has been shown that barbituric acid derivatives can be prepared in good yield by gradually adding sodium methoxide as condensation catalyst to a cyanoacetic or malonic ester reacting with urea or its derivatives. The principle of the gradual addition of sodium methoxide as condensing agent has now been extended to condensations of some substituted cyanoacetic and malonic esters with thiourea

    Thermodynamically self-consistent non-stochastic micromagnetic model for the ferromagnetic state

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    In this work, a self-consistent thermodynamic approach to micromagnetism is presented. The magnetic degrees of freedom are modeled using the Landau-Lifshitz-Baryakhtar theory, that separates the different contributions to the magnetic damping, and thereby allows them to be coupled to the electron and phonon systems in a self-consistent way. We show that this model can quantitatively reproduce ultrafast magnetization dynamics in Nickel.Comment: 5 pages, 3 figure

    Note on the Preparation of Some Thiobarbiturates

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    It has been shown that barbituric acid derivatives can be prepared in good yield by gradually adding sodium methoxide as condensation catalyst to a cyanoacetic or malonic ester reacting with urea or its derivatives. The principle of the gradual addition of sodium methoxide as condensing agent has now been extended to condensations of some substituted cyanoacetic and malonic esters with thiourea

    Adaptively time stepping the stochastic Landau-Lifshitz-Gilbert equation at nonzero temperature: implementation and validation in MuMax3

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    Thermal fluctuations play an increasingly important role in micromagnetic research relevant for various biomedical and other technological applications. Until now, it was deemed necessary to use a time stepping algorithm with a fixed time step in order to perform micromagnetic simulations at nonzero temperatures. However, Berkov and Gorn have shown that the drift term which generally appears when solving stochastic differential equations can only influence the length of the magnetization. This quantity is however fixed in the case of the stochastic Landau-Lifshitz-Gilbert equation. In this paper, we exploit this fact to straightforwardly extend existing high order solvers with an adaptive time stepping algorithm. We implemented the presented methods in the freely available GPU-accelerated micromagnetic software package MuMax3 and used it to extensively validate the presented methods. Next to the advantage of having control over the error tolerance, we report a twenty fold speedup without a loss of accuracy, when using the presented methods as compared to the hereto best practice of using Heun's solver with a small fixed time step.Comment: 9 pages, 9 figure

    Calorimetric Investigation of Grafting of Styrene and Methylmethacrylate onto Air-Preirradiated Polyethylene

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    All existing and widely used methods for measuring reaction rate of polymerization processes suffer from basic disadvantages including indirect measurement, insufficient accuracy and limited applicability. Their unsuitability is especially pronounced in the investigation of graft copolymerization reactions in which the accuracy of measurement could be affected even by the different properties of individual polymer samples. In this work a new method, calorimetry, free of mentioned disadvantages is generally proposed for investigation of polymerization processes and particularly its application to radiation induced grafting of styrene and methylmethacrylate onto polyethylene is demonstrated. Experimental results showed the possibility of calorimetry to measure the grafting rate continuously and directly in the whole conversion range with the accuracy much better than with any other method used so far. It was concluded that styrene grafting is non-diffusion-controlled, whereas methylmethacrylate grafting is not diffusion- independent. With both monomers the reaction kinetics was found to be dependent on the type of polyethylene a s a consequence of different mechanisms, i. e. in the initiation step two different species, peroxy radicals and peroxides, take part. Its concentration is different in two types of polyethylene used. In the case of high density polyethylene both active species participate in the initiation process equally, according to their different nature. However, in low density polyethylene the concentration of peroxy radicals is negligible compared to that of peroxides and therefore peroxides have dominating role in the initiation step of grafting reaction. The change of the viscosity of reaction medium in the course of reaction as well as the structure of polymer in the case of high density polyethylene influence the kinetics of grafting reaction

    Preparation of Some lmino- and Cyano-imino-substituted Barbiturates

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    A number of imino- and cyano-iminobarbituric acid derivatives has been prepared in good yield by gradually adding sodium methoxide - as condensation catalyst - to some substituted cyanoacetic and malonic esters reacting with urea, dicyandiamide and guanidine

    Preparation of Some lmino- and Cyano-imino-substituted Barbiturates

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    A number of imino- and cyano-iminobarbituric acid derivatives has been prepared in good yield by gradually adding sodium methoxide - as condensation catalyst - to some substituted cyanoacetic and malonic esters reacting with urea, dicyandiamide and guanidine

    O nusproduktima kod preparacije 5-etil-5-fenil-barbiturne kiseline

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    5-etil-5-fenil-barbiturna kiselina (luminal, fenobarfital) priprema se obicno kondenzacijom dietil etil-fenil-malonata (II) i uree u abs. etanolu uz Na-etoksid kao kondenzacino sredstvo. Relativno niska iskoristenja pripisuju se cijepanju dietil etil-fenil-malonata. Poznato je, naime, da disupstituirani malonski esteri u prisutnosti Na-etoksida dekarbetoksiliraju u odgovarajuce disupstituirane octene estere. Kod kondenzacije disupstituiranih malonata sa ureom uz Na-etoksid daje preostali malonat odgovarajuci barbiturat, a cijepanjem nastali acetat produkte reakcije sa ureom (ili amonijakom)
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