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91.
Preparation of high molecular weight polybenzoxazine prepolymers containing siloxane unites and properties of their thermosets 总被引:1,自引:0,他引:1
Tsutomu Takeichi Takuya Kano Tarek Agag Takehiro Kawauchi Nobuyuki Furukawa 《Journal of polymer science. Part A, Polymer chemistry》2010,48(24):5945-5952
High‐molecular‐weight polybenzoxazine prepolymers containing polydimethylsiloane unit in the main‐chain have been synthesized from α,ω‐bis(aminopropyl)polydimethylsiloxane (PDMS) (molecular weight = 248, 850, and 1622) and bisphenol‐A with formaldehyde. Moreover, another type of prepolymers was prepared using methylenedianiline (MDA) as codiamine with PDMS. The weight average molecular weight of the obtained prepolymers was estimated from size exclusion chromatography to be in the range of 8000–11,000. The chemical structures of the prepolymers were investigated by 1H NMR and IR analyses. The prepolymers gave transparent free standing films by casting their dioxane solution. The prepolymer films after thermally cured up to 240 °C gave brown colored transparent and flexible polybenzoxazine films. Tensile test of the films revealed that the elongation at break increased with increasing the molecular weight of PDMS unit. Dynamic mechanical analysis of the thermosets showed that the Tgs were as high as 238–270 °C. The thermosets also revealed high thermal stability as evidenced by the 5% weight loss temperatures in the range of 324–384 °C from thermogravimetic analysis. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 相似文献
92.
Tarek M. Trad Kyle B. Donley David C. Look Kurt G. Eyink David H. Tomich Curtis R. Taylor 《Journal of Crystal Growth》2010,312(24):3675-3679
ZnO nanoparticles as small as 80 nm were successfully synthesized using a modified vapor phase transport (VPT) process at substrate temperatures as low as 222 °C. Particle size distribution and morphology were characterized by scanning electron microscopy and atomic force microscopy. Energy dispersive X-ray spectroscopy and X-ray diffraction indicate the synthesis of high quality crystalline ZnO structures. Low temperature (4.2 K) photoluminescence (PL) spectroscopy was used to characterize the optical quality of the nanoparticles. Ultraviolet emission and a nanostructure specific feature at 3.366 eV are strong in the PL spectra. The 3.366 eV feature is observed to predominate the spectrum with decrease in particle size. This size effect corroborates the luminescence as a nanostructure-specific surface related exciton feature as previously speculated in the literature. In addition, self-assembled ZnO mesoparticles (>100 nm) were realized by increasing the growth time. Low growth temperatures of the particles allow for their potential utilization in flexible organic hybrid optoelectronics. However, this work focuses mainly on the modified synthesis and optical characterization of nanoparticles. 相似文献
93.
The electrochemical oxidation of the three fluoroquinolone drugs FQs: gatifloxacin GTF, moxifloxacin MXF and sparfloxacin SPF, at the bare and DNA‐modified glassy carbon electrodes has been studied by voltammetric techniques. The three FQs showed one irreversible oxidation peak at potential range 0.85–0.91 V vs. Ag‐AgCl, in phosphate buffer of pH 7.0. Differential pulse voltammetry (DPV) and UV‐absorption spectroscopic techniques were employed to probe the interaction between the FQs and calf thymus double stranded deoxyribonucleic acid (ds CT‐DNA). From electrochemical data, the binding constant between DNA and the gatifloxacin, moxifloxacin and sparfloxacin are calculated to be 3228, 2596 and 2857 M?1 respectively. Based on electrochemical and spectroscopic results, the mode of binding of fluoroquinolone to DNA through combined effect of intercalation and electrostatic interaction was concluded. A detection scheme based on a preconcentration and differential pulse voltammetric (DPV) determination at dsDNA modified glassy carbon electrode (DNA/GCE) was proposed for the trace determination of the studied analytes. The developed method was successfully applied to the determination of the FQs in pharmaceutical formulations. 相似文献
94.
Simple, rapid, and selective RP-HPLC methods with UV detection were developed for simultaneous determination of chlordiazepoxide hydrochloride and mebeverine hydrochloride (Mixture I) and carvedilol and hydrochlorothiazide (Mixture II). The chromatographic separation in both mixtures was achieved by using an RP-C8 (octylsilyl) analytical column. For Mixture I, a mobile phase composed of acetonitrile-0.05 M disodium hydrogen phosphate-triethylamine (50 + 50 + 0.2, v/v/v), pH 2.5, was used; the detector wavelength was 247 nm. For Mixture II, the mobile phase consisted of acetonitrile-0.05 M disodium hydrogen phosphate (50 + 50, v/v), pH 4.0, and the detector was set at 220 nm. Quantification of the analytes was based on measuring their peak areas. Both mixtures were resolved in less than 6 min. The reliability and analytical performance of the proposed HPLC procedures were statistically validated with respect to linearity, range, precision, accuracy, selectivity, robustness, LOD, and LOQ. The linear dynamic ranges were 2.5-150 and 2.5-500 microg/mL for chlordiazepoxide HCI and mebeverine HCI, respectively, and 0.25-200 and 0.25-150 microg/mL for carvedilol and hydrochlorothiazide, respectively. The validated HPLC methods were successfully applied to the analysis of their commercial tablet dosage forms, for which no interfering peaks were encountered from common pharmaceutical adjuvants. 相似文献
95.
Tarek Hamdi 《Complex Analysis and Operator Theory》2018,12(7):1697-1705
The present paper provides a proof of \(i^*(\mathbb {C}P+\mathbb {C}(I-P); \mathbb {C}Q+\mathbb {C}(I-Q))=-\chi _{{ orb}}(P,Q)\) for two projections P, Q without any extra assumptions. An analytic approach is adopted to the proof, based on a subordination result for the liberation process of symmetries associated with P, Q. 相似文献
96.
The absorption and fluorescence characteristics of (4‐dimethylamino‐benzylidene)‐(4,6‐dimethyl‐pyrimidin‐2‐yl)‐amine (SB) have been investigated in different solvents. Both the absorption and emission spectra of SB exhibit red shifts as the solvent polarity increases. This indicats a change in dipole moment of molecules upon excitation as a result of intramolecular charge transfer interaction. The fluorescence quantum yield depends strongly on the properties of the solvents, which was discussed on the bases of positive and negative solvatokinetic effects. The effect of some divalent transition metal ions such as Mn2+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+, and Hg2+on the absorption and fluorescence spectra of SB is also investigated. The results were consistent with formation of highly colored metal‐ SB complex which is responsible for the extreme quenching of the fluorescence of SB. The variations of both the formation constant of the complex and Stern‐Volmer constant were correlated with the electronic structure of the used metal ion. 相似文献
97.
Tarek Sayed Ahmed 《Mathematical Logic Quarterly》2008,54(3):294-306
Letn > 2. A weakly representable relation algebra that is not strongly representable is constructed. It is proved that the set of all n by n basic matrices forms a cylindric basis that is also a weakly but not a strongly representable atom structure. This gives an example of a binary generated atomic representable cylindric algebra with no complete representation. An application to first order logic is given. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
98.
Tarek Sayed Ahmed 《Algebra Universalis》2010,63(1):17-36
This is a survey article on the concept of neat reducts. An old venerable idea in algebraic logic, in this paper we show why
it is regaining momentum. 相似文献
99.
Tarek Agag Tsutomu Takeichi 《Journal of polymer science. Part A, Polymer chemistry》2007,45(10):1878-1888
Novel high‐molecular‐weight polybenzoxazine precursors, namely AB‐type benzoxazine precursors, were synthesized from aminophenols and formaldehyde. Both 1H NMR and IR confirmed the structure of the precursors, indicating the presence of a cyclic benzoxazine structure in the backbone of the precursors. The weight‐average molecular weight was estimated by size exclusion chromatography to be to in the range of 1300–4500. The precursors gave self‐standing thin films when their solutions were cast in dioxane over glass plates and dried, and upon a gradual thermal cure up to 250 °C, they afforded polybenzoxazine films. The viscoelastic analyses showed that the glass transition temperatures of the polybenzoxazine films obtained from these novel precursors were as high as 260–300 °C. Thermogravimetric analysis results indicated that the onset of decomposition and the char yield of the thermosets derived from these AB‐type precursors were higher than those of traditional polybenzoxazine. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 1878–1888, 2007. 相似文献
100.
Tarek A. Salama Bernd Lackner Heinz Falk 《Monatshefte für Chemie / Chemical Monthly》2003,32(5):1113-1119
An efficient synthesis of tri-O-methylemodin aldehyde was achieved via bromination of tri-O-methylemodin utilizing N-bromosuccinimide yielding the monobromo and dibromo derivatives. Sommelet reaction of the monobromomethyl derivative as well as hydrolysis of the dibromomethyl analog with aqueous silver nitrate afforded the protected aldehyde in good yield. Accordingly, both bromo derivatives can be used even when they are obtained as a mixture of the bromination reaction, which could not be controlled easily to yield the bromo products selectively. From the aldehyde the tri-O-methylemodin nitrile was prepared in a one-pot reaction using hydroxylamine-O-sulfonic acid. 相似文献