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941.
In this study, a simple and efficient way is demonstrated to create strong interfacial interaction between graphene oxide(GO) filler and poly(vinyl alcohol)(PVA) matrix through metal ion coordination. The coordination bonding provides efficient load transfer during the tensile process, and enhances the mechanical properties of the nanocomposites significantly. After being coordinated with Cu(Ⅱ) ions, GO/PVA composites show much higher Young's moduli and yield stresses than pure PVA and noncoordinated GO/PVA. UV–vis and FTIR spectra are performed to confirm the successful coordination between GO and PVA. Ethylene diamine tetraacetic acid disodium salt(EDTA-2 Na) is used to confirm the important role of coordination in enhancing the composites. This research provides a new approach to manufacture polymer-matrix nanocomposites with significantly improved mechanical performances. 相似文献
942.
943.
Sajjad Rashidi Farshad Farzin Mehdi Shanbedi Masoud Rahimipanah Maryam Savari 《Journal of Dispersion Science and Technology》2016,37(9):1277-1286
In order to enhance the thermal properties of turbine oil (TO), three different nanoparticles (CuO, Al2O3, and TiO2) are loaded into the TO. To measure the thermal performance of nanoparticle-based TO nanofluids at laminar flow and under constant heat flux boundary conditions, an experimental setup was applied. The obtained data clearly demonstrate the positive effect of all nanoparticles on the heat transfer rate of TO. As the most important factor, the heat transfer coefficient of the abovementioned two-phase systems is increased upon increasing both the volume concentration and the flow rate. An adaptive neuro-fuzzy inference system (ANFIS) is applied for modeling the effect of critical parameters on the heat transfer coefficient of nanoparticle-TO based nanofluids numerically. The results are compared with experimental ones for training and test data. The results suggest that the developed model is valid enough and promising for predicting the extant of the heat transfer coefficient. R2 and MSE values for all data were 0.990208751 and 108.1150734, respectively. Based on the results, it is obvious that our proposed modeling by ANFIS is efficient and valid, which can be expanded for more general states. 相似文献
944.
以聚苯醚(PPO)为基体材料, 通过溴甲基化及咪唑基团功能化, 与聚四氟乙烯(PTFE)复合、 硅氧烷基团水解交联及磷酸掺杂, 制备了兼具高磷酸掺杂含量、 高质子电导率和良好机械性能的高温质子交换膜材料. 以甲基咪唑(MeIm)和咪唑基硅氧烷化合物(SiIm)为功能化试剂(其中咪唑基团提供了磷酸作用位点, 同时SiIm中的硅氧烷基团水解后得到Si—O—Si交联网络结构), 提高了膜材料的机械稳定性. 与PTFE的复合进一步增强了膜材料的机械强度. 结果表明, 复合膜具有较高的电导率和一定的机械强度. 当磷酸掺杂质量分数为242.5%时, PPO-50%SiIm-50%MeIm/PTFE复合膜在160 ℃不加湿条件下的电导率为0.09 S/cm, 室温下的断裂拉伸强度为3.6 MPa. 相似文献
945.
Ambrish Kumar Srivastava 《Molecular physics》2018,116(12):1642-1649
Benzene (C6H6) and polycyclic hydrocarbons such as naphthalene (C10H8), anthracene (C14H10) and coronene (C24H12) are well known aromatic organic compounds. We study the substitution of Li replacing all H-atoms in these hydrocarbons using density functional method. The vertical ionisation energy of such lithiated species, i.e. C6Li6, C10Li8, C14Li10 and C24Li12 ranges 4.24–4.50 eV, which is lower than the ionisation energy (IE) of Li atom. Thus, these species may behave as superalkalis due to their lower IE than alkali metal. However, these lithiated species possess planar and closed-shell structure, unlike typical superalkalis. Furthermore, all Li-substituted species are aromatic although their degree of aromaticity is reduced as compared to corresponding hydrocarbon analogues. We have further explored the structure of C6Li6 as star-like, unlike its inorganic analogue B3N3Li6, which appears as fan-like structure. We have also demonstrated that the interaction of C6Li6 with a superhalogen (such as BF4) is similar to that of a typical superalkali (such as OLi3). This may further suggest that the proposed lithiated species may form a new class of closed-shell organic superalkalis with aromaticity. 相似文献
946.
Gunawan Gunawan Tito Viswanathan Shawn Bourdo Alexandru S. Biris 《Phosphorus, sulfur, and silicon and the related elements》2013,188(6):768-777
Abstract A novel, fast, and easy method for synthesizing a carbon-supported Ni2P nanocomposite (C/Ni2P) is described. The process involves a reaction between a nickel salt, phosphoric acid, and a carbon source by utilizing microwave irradiation. The carbon source for the nanocomposite is from renewable supplies, namely, tannin and lignin. The method has successfully synthesized Ni2P nanoparticles dispersed in a carbon matrix with a particle size ranging from 20 to 50 nm in diameter. During the microwave process, tannin and lignin provided a reducing environment in the microwave irradiation process. The synthesized products are characterized by several characterization methods. The method showed that phosphoric acid, which is a nontoxic compound, could be used as an alternative P source for synthesizing Ni2P. The method is fast, easy, and an economical process to synthesize the carbon-coated Ni2P nanocomposite. 相似文献
947.
Controlling domain orientation of liquid crystalline block copolymer in thin films through tuning mesogenic chemical structures 下载免费PDF全文
He‐Lou Xie Xiao Li Jiaxing Ren Camille Bishop Christopher G. Arges Paul F. Nealey 《Journal of Polymer Science.Polymer Physics》2017,55(6):532-541
Controlling the macroscopic orientation of nanoscale periodic structures of amphiphilic liquid crystalline block copolymers (LC BCPs) is important to a variety of technical applications (e.g., lithium conducting polymer electrolytes). To study LC BCP domain orientation, a series of LC BCPs containing a poly(ethylene oxide) (PEO) block as a conventional hydrophilic coil block and LC blocks containing azobenzene mesogens is designed and synthesized. LC ordering in thin films of the BCP leads to the formation of highly ordered, microphase‐separated nanostructures, with hexagonally arranged PEO cylinders. Substitution on the tail of the azobenzene mesogen is shown to control the orientation of the PEO cylinders. When the substitution on the mesogenic tails is an alkyl chain, the PEO cylinders have a perpendicular orientation to the substrate surface, provided the thin film is above a critical thickness value. In contrast, when the substitution on the mesogenic tails has an ether group the PEO cylinders assemble parallel to the substrate surface regardless of the film thickness value. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2017 , 55, 532–541 相似文献
948.
949.
K. Runge 《Isotopes in environmental and health studies》2013,49(4):176-177
Neben ihrer breiten Anwendung in der Nuklearmedizin gewinnen Radionuklidgeneratoren zunehmend auch für die verfahrensctechnische Forsehung Bedeutung. Es konnte gezeigt warden, daß die Generatorsysteme 99Mo/99mTe und 113Sn/113mI für zahlreiche Untersuchungen von Transportund Mischvorgängen in technischen Anlagen genutzt warden könnea [1, 2]. Der Radionuklidgenerator 110Ba/110La hat für den Einsatz in der Technik günstigere Eigenschaftcn als die für die Nuklearmedizin entwickelten Generatoren. Insbesondere für die Untersuchung der Materialtransportvorgänge in Polykondensationsreaktoren der Chemiefaserindustrie hat sich ein Lanthan-140-Generator gut bewährt, der mit Tributylphosphat (gesättigt mit 13 N HN03) als Elutionsmittel arbeitet [3, 4]. 相似文献
950.