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21.
Polyimide nanocomposites having low-k and UV shielding properties have been developed using fluorine functionalized graphene oxide and bis(quinoline amine) based polyimide. The polyimide was synthesized using bis(quinoline amine) and pyromellitic dianhydride at appropriate experimental conditions, and its molecular structure was confirmed through various spectral analysis such as FTIR and NMR. The polyimide (PI) composites were prepared using bis(quinoline amine), pyromellitic dianhydride, and separately filled with 1, 5, 10 wt% of fluorinated graphene oxide (FGO) through in situ polymerization. The polymer composites were characterized using thermo gravimetric analysis (TGA), X-ray powder diffraction (XRD), and scanning electron microscopy (SEM). In addition, the water contact angle, dielectric behavior, and UV–Vis shielding behavior of FGO/PI composites were evaluated. The value of the water contact angle of the polyimide was increased with increment of FGO in the polyimide matrix. The highest water contact angle of polyimide composites observed 108° was obtained for 15 wt% FGO reinforced polyimide composite. The value of the dielectric constant for neat, 1, 5, and 15 wt% FGO reinforced polyimide composites was obtained as 4.5, 3.7, 2.6, and 2.0, respectively. It is also observed from by UV–Vis spectroscopy analysis that the FGO reinforced polyimide composites have good UV shielding behavior. 相似文献
22.
Theoretical Investigations on Photodissociation Dynamics of Deuterated Alkyl Halides CD3CH2F 下载免费PDF全文
The product branching ratio between different products in multichannel reactions is as important as the overall rate of reaction, both in terms of practical applications (\emph{e.g}. models of combustion or atmosphere chemistry) in understanding the fundamental mechanisms of such chemical reactions. A global ground state potential energy surface for the dissociation reaction of deuterated alkyl halide CD\begin{document}$ _3 $\end{document} CH\begin{document}$ _2 $\end{document} F was computed at the CCSD(T)/CBS//B3LYP/aug-cc-pVDZ level of theory for all species. The decomposition of CD\begin{document}$ _3 $\end{document} CH\begin{document}$ _2 $\end{document} F is controversial concerning C\begin{document}$ - $\end{document} F bond dissociation reaction and molecular (HF, DF, H\begin{document}$ _2 $\end{document} , D\begin{document}$ _2 $\end{document} , HD) elimination reaction. Rice-Ramsperger-Kassel-Marcus (RRKM) calculations were applied to compute the rate constants for individual reaction steps and the relative product branching ratios for the dissociation products were calculated using the steady-state approach. At the different energies studied, the RRKM method predicts that the main channel for DF or HF elimination from 1, 2-elimination of CD\begin{document}$ _3 $\end{document} CH\begin{document}$ _2 $\end{document} F is through a four-center transition state, whereas D\begin{document}$ _2 $\end{document} or H\begin{document}$ _2 $\end{document} elimination from 1, 1-elimination of CD\begin{document}$ _3 $\end{document} CH\begin{document}$ _2 $\end{document} F occurs through a direct three-center elimination. At 266, 248, and 193 nm photodissociation, the main product CD\begin{document}$ _2 $\end{document} CH\begin{document}$ _2 $\end{document} +DF branching ratios are computed to be 96.57%, 91.47%, and 48.52%, respectively; however, at 157 nm photodissociation, the product branching ratio is computed to be 16.11%. Based on these transition state structures and energies, the following photodissociation mechanisms are suggested: at 266, 248, 193 nm, CD\begin{document}$ _3 $\end{document} CH\begin{document}$ _2 $\end{document} F\begin{document}$ \rightarrow $\end{document} absorption of a photon\begin{document}$ \rightarrow $\end{document} TS5\begin{document}$ \rightarrow $\end{document} the formation of the major product CD\begin{document}$ _2 $\end{document} CH\begin{document}$ _2 $\end{document} +DF; at 157 nm, CD\begin{document}$ _3 $\end{document} CH\begin{document}$ _2 $\end{document} F\begin{document}$ \rightarrow $\end{document} absorption of a photon\begin{document}$ \rightarrow $\end{document} D/F interchange of TS1\begin{document}$ \rightarrow $\end{document} CDH\begin{document}$ _2 $\end{document} CDF\begin{document}$ \rightarrow $\end{document} H/F interchange of TS2\begin{document}$ \rightarrow $\end{document} CHD\begin{document}$ _2 $\end{document} CHDF\begin{document}$ \rightarrow $\end{document} the formation of the major product CHD\begin{document}$ _2 $\end{document} +CHDF. 相似文献
23.
Nanocomposites comprising flexible polymers and high dielectric constant inorganic nanoparticles are considered to be one of the promising candidates for electrostatic capacitor dielectrics.However,the effect of interfacial property on electrical ene rgy storage of dielectric polymer nanocomposites is still not clear.Herein,the role of the polarity of the interfacial region is investigated.For this purpose,three polymers with different polarity,polymethyl methacrylate(PMMA),polyglycidyl methacrylate,and polymethylsulfonyl ethyl methacrylate(PMSEMA) are attached onto BaTi03(BT) na noparticle surface via surface-initiated reversible addition-fragmentation chain transfer polymerization.It is found that the polarity of shell polymers shows an apparent effect on the dielectric and energy storage of dielectric polymer nanocomposites.For example,PMSEMA@BT(shell polymer possesses the highest polarity)increases dielectric loss and decreases the breakdown strength of the nanocomposites,leading to lower ene rgy storage capability.However,PMMA@BT(shell polymer possesses the lowest polarity) can induce higher breakdown strength of the nanocomposites.As a result,the PMMA@BT nanocomposite exhibits the highest electrical energy sto rage capability among the three nanocomposites.This re search provides new insight into the design of core-shell nanofillers for dielectric energy storage applications. 相似文献
24.
Hong-Jing YU Wen-Wen XIA Li-Guo SONG Yang DING Yu HAO Li-Qiang KANG Xin-Xiang PAN Li YAO 《物理化学学报》2017,33(11):2207-2218
In this work, the harmonic and anharmonic rate constants of the decomposition reaction of monomethylhydrazine (MMH) radicals have been calculated by using transition state (TS) and Rice-Ramsperger-Kassel-Marcus (RRKM) theories with either MP2 or B3LYP method at 6-311++G (3df, 2p) basis set, respectively. The reaction mechanism and anharmonic effect of the MMH radicals are studied in detail and both of the harmonic and anharmonic rate constants increase sharply with increasing temperature in the canonical system. In the microcanonical system, these constants also show sharp increase with the energies. Overall, the anharmonic effect becomes more pronounced with the increasing temperature or energy in the canonical and microcanonical systems, respectively. These results indicate that the anharmonic effect of the decomposition reaction of MMH radicals is quite significant and cannot be ignored. 相似文献
25.
研究了二元叠加码Mq(t,k,d)也是一个二元等重码,给出了它成为最佳等重码的条件,研究了它的检错性. 相似文献
26.
A Markov observation model with dividend is defined and the interpretation of the practical significance is given. We try to use an irreducible and homogeneous discrete-time Markov chain to modulate the inter-observation times and embed a dividend strategy. In the Markov observation model with dividend, a system of liner equations for the expected discounted value of dividends until ruin time is derived. Moreover, an explicit expression is obtained and proved. Finally, some interesting properties are illustrated by numerical analysis and by comparing with the complete compound binomial model with dividend. 相似文献
27.
This note is denoted to establishing sharp distortion theorems for subclasses of α-Bloch mappings defined in the unit ball of Cn with critical points.Furthermore,the estimates of Bloch constant with respect to these subclasses are given. 相似文献
28.
Song and Mason equation of state (EOS) with a simple modification has been extended to modelling PVT properties of ionic liquids (ILs). The considered ILs are [C1mim][MeSO4], [C1mim][CH3OC2H5SO4], [C1mim][(CH3)2PO4], [C2mim][MeSO4], [C2mim][BF4], [C2mim][SCN], [C2eim][NTf2], [C4mim][C(CN)3], [C4mim][CF3SO3], [C4mim][SCN], [C5mim][NTf2], [C8mim][NTf2], [(C6H13)3P(C14H29)][Cl], [(C6H13)3P(C14H29)][NTf2], [(C6H13)3P(C14H29)][Ac], [C3mpyr][NTf2], [C4mpyr][NTf2] and [Py][C2H5OC2H4SO4]. Three temperature-dependent parameters in the proposed EOS have been scaled as functions of reduced temperature with the use of the law of corresponding states. It is shown that the knowledge of just critical temperature and critical density is sufficient to predict the PVT properties of these ILs. The overall average absolute deviation of calculated densities from literature values for 1347 data points of 18 ILs was found to be 0.58%. The predicted density of ILs from proposed EOS has been compared with those obtained by other literature work. Moreover, we indicate that the Zeno line regularity can well be predicted by proposed model for ILs. 相似文献
29.
A novel thiophene attached anthracene (TA) based fluorescent compound was designed and synthesized. The TA showed a high quantum yield (Qy = 0.34) in regard to fluorescence. We applied this TA compound to detect specific metal compound and found that it could identify CuCl2 from other metals through dramatic fluorescence change at λmax = 460 nm. It showed strong quenching fluorescence property with CuCl2 while with other metal compounds it exhibited strong blue fluorescence emission. UV/Vis absorption spectroscopy clearly demonstrated that the quenching property of TA at λmax = 460 nm was due to overlapping of the fluorescence peak of TA at λmax = 460 nm and the absorption band of CuCl2 (from 190 nm to 525 nm). Binding constant (K′), which was 0.0895 mM?2, indicated a complexation ratio between TA and CuCl2 as 1:2 and this interaction induced quenching property. 相似文献
30.
Summary of ISO/TC 201 standard: ISO 11775:2015 – Surface chemical analysis – Scanning probe microscopy – Determination of cantilever normal spring constants 下载免费PDF全文
Charles A. Clifford 《Surface and interface analysis : SIA》2017,49(3):171-172
This International Standard describes five methods for the determination of normal spring constants for atomic force microscope cantilevers to an accuracy of 5 to 10%. Each method is in one of the three categories of dimensional, static experimental and dynamic experimental methods. The method chosen depends on the purpose, convenience and instrumentation available to the analyst. For accuracies better than 5 to 10%, more sophisticated methods, not described in the standard, are required. Copyright © 2016 Crown copyright. Surface and Interface Analysis © 2016 John Wiley & Sons, Ltd. 相似文献