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51.
Ecaterina Stela Dragan Ionel Adrian Dinu Marcela Mihai 《Colloids and surfaces. A, Physicochemical and engineering aspects》2009,348(1-3):282-288
The interaction between strong polycations, which possess the ammonium quaternary centers attached to an acrylic macromolecular chain derived from poly(N,N-dimethylaminoethyl methacrylate) (polycations Qx), and divalent counterions was investigated by viscometry and turbidimetry. Conformational changes of polycations were influenced by the polycation charge density, counterion nature (SO42− or S2O82−) and concentration. The morphology of the polycation layers deposited onto silicon wafers has been studied by tapping mode atomic force microscopy, a strong influence of the polycation and ammonium persulfate concentration on the surface topography being observed. The optimum flocculation concentration of polycation decreased and the flocculation window increased in the presence of S2O82−, in the destabilization of kaolin model dispersion. Removal of Congo Red from aqueous solution by the complex system formed between polycations and divalent counterions was also investigated. The behavior of polycations Qx in separation processes was compared with that of one polycation containing 95 mol% N,N-dimethyl-2-hydroxypropyleneammonium chloride units in the backbone (PCA5). 相似文献
52.
Thallada Bhaskar Kazuya Murai Toshiki Matsui Mihai Adrian Brebu Md. Azhar Uddin Akinori Muto Yusaku Sakata Katsuhide Murata 《Journal of Analytical and Applied Pyrolysis》2003,70(2):369-381
The thermal degradation of acrylonitrile-butadiene-styrene copolymer (ABS-Br; 10 g) containing brominated flame retardant (Br: 9.59 wt.%) was carried out at 450 °C using a semi batch operation using two different temperature programs. The heating rate was found to affect the quality of the degradation oil and yield of products (liquid, gas and residue). Data on the effect of the temperature program on the accumulation of liquid products was presented. It was found that the majority of the bromine was concentrated in the carbon residue and while majority of the nitrogen accumulates in the liquid products irrespective of degradation mode. The use of a one step constant heating rate process (I) produced a higher liquid yield (39%), than a two step process (29%). Differences were also noted in the Br and N contained in the liquids produced by the two processes. 相似文献
53.
Periodica Mathematica Hungarica - 相似文献
54.
Mihai Mihăilescu Gheorghe Moroşanu 《Nonlinear Analysis: Real World Applications》2013,14(3):1466-1476
This paper investigates a nonlinear and non-homogeneous system of partial differential equations. The motivation comes from the fact that in a particular case the problem discussed here can be used in modeling the behavior of nonlinear Hencky-type materials. The main result of the paper establishes the existence of a nontrivial solution in an adequate functional space of Orlicz–Sobolev type by using Schauder’s fixed point theorem combined with adequate variational techniques. 相似文献
55.
Robert J. Bellair Mihai Manitiu Esin Gulari Rangaramanujam M. Kannan 《Journal of Polymer Science.Polymer Physics》2010,48(8):823-831
Superior property enhancements in polymer–clay nanocomposites can be achieved if one can significantly enhance the nanoclay dispersion and polymer–clay interactions. Recent studies have shown that nanoclays can be dispersed in polymers using supercritical carbon dioxide (scCO2). However, there is need for a better understanding of how changing the clay modifier affects the clay dispersability by scCO2 and the resultant nanocomposite rheology. To address this, the polystyrene (PS)/clay nanocomposites with “weak” interaction (Cloisite 93A clay) and “strong” interaction (Cloisite 15A clay) have been prepared using the supercritical CO2 method in the presence of a co‐solvent. Transmission electron microscopy images and small‐angle X‐ray diffraction illustrate that composites using 15A and 93A clays show similar magnitude of reduction in the average tactoid size, and dispersion upon processing with scCO2. When PS and the clays are coprocessed in scCO2, the “dispersion” of clays appears to be independent of modifier or polymer–clay interaction. However, the low‐frequency storage modulus in the scCO2‐processed 15A nanocomposites is two orders of magnitude higher than that of 93A nanocomposites. It is postulated that below percolation (solution blended composites), the strength of polymer–clay interaction is not a significant contributor to rheological enhancement. In the scCO2‐processed nanocomposites the enhanced dispersion passes the percolation threshold and the interactions dictate the reinforcement potential of the clay–polymer–clay network. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 823–831, 2010 相似文献
56.
57.
I. Chiorean A. B. Németh C. I. Gheorghiu Mihai Putinar V. Kalashnikov 《Acta Appl Math》1994,35(3):299-302
58.
Björn Gustafsson Mihai Putinar 《Journal of Mathematical Analysis and Applications》2007,328(2):995-1006
The analytic continuation of the exponential transform of a domain in Rn is proved under some global geometric assumptions on the boundary. Two approximation schemes of the continued transform (one based on a Taylor series truncation, the other on a global eigenfunction expansion) are also discussed. 相似文献
59.
60.
Ecaterina Stela Dragan Marcela Mihai J. Schauer Luminita Ghimici 《Journal of polymer science. Part A, Polymer chemistry》2005,43(18):4161-4171
Polyacrylonitrile (PAN) composite membranes with surface properties designed by either a chemical modification with ethylenediamine (EDA), or layer‐by‐layer (LbL) polyelectrolyte adsorption were investigated in this paper. Fourier‐transformed infrared (FTIR) spectroscopy and streaming potential measurements showed that the first step of the reaction with EDA in gas phase was the formation of ammonium salts with the reactive carboxylic groups present on the surface of the starting membrane. Part of the ammonium carboxylate groups was transformed in secondary amide linkages by a heat‐induced reaction. Poly(sodium styrenesulfonate) (NaPSS) and a polycation containing about 95 mol % of N,N‐dimethyl‐2‐hydroxypropyleneammonium chloride units in the backbone (PCA5) were used as opposite polyions in the LbL film construction. The adsorbed polyion amount per every layer was controlled by the nature and concentration of the supporting electrolyte in polyelectrolyte deposition solution (NaBr and KBr). An almost linear increase of the adsorbed polyion amount versus the layer pair number was observed. The swelling degree (SD) in pure alcohols of the LbL‐modified PAN composite membrane decreased with the increase of the solvent polarity and with the decrease of the pore volume by pore filling with polyelectrolyte complex multilayer. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 4161–4171, 2005 相似文献