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851.
We analyze the so-called word-problem for , the ring of matrices over . We prove that the term-equivalence problem for the semigroup (and so for the ring) is coNP-complete.

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852.
Different samples of aminated latex of poly(styrene-co-Boc-aminostyrene) microspheres with mean diameters varying from 0.7 to 1.0 microm were prepared by dispersion copolymerization of styrene (ST) and Boc-aminostyrene (Boc-AMST). The copolymer compositions determined by nuclear magnetic resonance (1H NMR) were Boc-AMST/ST 6.9/93.1 mol/mol % (BOC7 sample) and Boc-AMST/ST 31.3/68.7 mol/mol % (BOC30 sample). The average molecular weights determined by gel permeation chromatography were 126 kDa (BOC7 sample) and 51 kDa (BOC30 sample). The latex containing NH-carbo-tert-butoxy groups (NH-Boc) were treated with 2 M HCl in isopropyl alcohol/water (1:1 vol/vol), at 50 degrees C for 3, 6, 9, 24, and 30 h, in order to control the extent of deprotection reaction of the NH-Boc. The deprotection reaction resulted in the formation of NH3+Cl- groups on the particle surfaces. The kinetic of the deprotection reaction was investigated by 1H NMR analyses and the yield varied from 20 to 40%. The resulting -NH3+Cl- groups on the microsphere surfaces were examined, in particular, by electron spectroscopy imaging (ESI) using an energy-filtered transmission electron microscope (EFTEM) that clearly demonstrated the presence of Cl on the particle surfaces. Scanning electron photomicrographs recorded for the above samples showed that the particle morphology was maintained after the acidic treatment.  相似文献   
853.
The interaction between proteins and solid surfaces has been investigated. The aim of this work is to compare three different materials (hydroxyapatite, polystyrene with core-shell structure (PE-CS) and a functionalized styrene divinylbenzene copolymer) to be used as adsorbents for lysozyme, known as a “hard” protein. Tests were performed according to an experimental design in order to compare the effects of pH, lysozyme and phosphate buffer concentration onto the adsorbed amount of protein. A 23 factorial design and a cross design, which was performed in triplicate, were used to distinguish the most important variables and to infer about the interaction between them. Hydroxyapatite showed the best performance—higher adsorbed amount of lysozyme and smaller dispersion (72.2 ± 0.9 mg/g). However, PE-CS can be regarded as a promising support as high amounts of lysozyme are adsorbed onto this material with relatively small dispersion.  相似文献   
854.
The delayed ion extraction method has been used to study characteristics of the initial velocity distributions of positive and negative ions produced simultaneously by laser desorption/ionization (LDI) from non-impacted single aerosol polymeric particles, using a bipolar time-of-flight (TOF) instrument (LAMPAS 2). Due to the geometry of the setup and the characteristics of the ablation process, only the projections of the velocities on the axis of the mass spectrometer can be directly studied. Additionally, since the mean initial velocity under these conditions should be close to zero, it was necessary to extend the method by taking into account higher order contributions of the velocity distribution. Theoretical expressions for these higher order terms are presented and discussed. The bipolar characteristics of the instrument permit evaluation and treatment of a possible instrumental artifact caused by small inclinations of the ionizing laser with respect to the ideal incidence direction. Results of a number of experiments are presented and discussed in relation to the theoretical expressions presented, and to possible ablation scenarios. Evidence pointing out that, under our experimental conditions, only partial ablation of the latex particles occurs was obtained. The variance of the distribution of the projection of the initial velocities can be directly estimated from these results. By assuming that the total initial velocities of the ions are developed completely according to a single-temperature adiabatic expansion mechanism, temperatures of approximately 50 K/Da can be assigned to the ion clouds from the variance estimations. If a two-temperature model is used, a radial temperature of about 100 K/Da results. These values are in reasonable agreement with results for polymer ablation from the literature.  相似文献   
855.
The formation of 3-(2-nitrophenyl)pyruvic acid and its amide and ester derivatives – key compounds for the Reissert indole synthesis – was achieved under various reaction conditions via the acid catalyzed hydrolysis of 5-(2-nitrobenzyliden)-2,2-dimethyl-1,3-oxazolidin-4-one, which is readily available from 3-(2-nitrophenyl)oxirane-2-carboxamide. A new and highly efficient method for the synthesis of indole-2-carboxylic acid derivatives via the intramolecular reductive cyclization of o-nitrophenylpyruvic acid and its amide and ester derivatives was developed using Na2S2O4 in dioxane/water at reflux.  相似文献   
856.
857.
858.
Journal of Thermal Analysis and Calorimetry - Poly(butylene succinate) (PBS) nanocomposites filled with nanoprecipitated calcium carbonate (NPCC) were prepared via melt blending. The hybrid...  相似文献   
859.
The aim of this article is to provide second-order sufficiency criteria that extend known ones in [6] and [7] to the case where the control candidate and some of the data are merely essentially bounded, and/or the control setU is any convex subset of m . In the classical setting, where a restriction on the velocity is imposed , it is shown that whenU is compact the known strengthened Weierstrass condition is equivalent to the Weierstrass condition with strict inequality.The research was supported by an NSERC Grant and by GNAFA of CNR, which are gratefully acknowledged.  相似文献   
860.
Summary. An efficient protocol for the preparation of phenylselenoethers from unsaturated alcohols using phenylselenenyl halides at room temperature was developed. The procedure employs phenylselenenyl chloride and bromide, some Δ 4- and Δ 5-alkenols and Ag2O, as an additive, to generate the tetrahydropyrans or tetrahydrofurans. This method permits the preparation of cyclic phenylselenoethers in high yields and under extremely mild conditions.  相似文献   
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