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951.
Aouatef Ladhari Hedi Belhadjsalah Johanne Denault 《Polymer Degradation and Stability》2010,95(4):429-13298
The behaviour of polypropylene nanocomposites containing different amounts of commercial nanoclay upon exposure to distilled water and sea water at different temperatures was investigated and compared with that of neat polypropylene. In the initial stages, the weight gain (moisture absorption) follows Fick's second law, but at longer times deviations are observed owing to physical degradation and in some cases a loss of mass. Distilled water diffuses more rapidly than sea water. As the nanoclay content increases, both the rate of moisture absorption and the maximum moisture content increase, owing to the hydrophilic nature of the nanoclay and the added compatibilizing agent. Although the moisture absorption decreases the flexural properties of both the nanocomposites and neat PP, because the unexposed (as-moulded) nanocomposites are significantly superior to the neat PP they remain so even after prolonged exposure. 相似文献
952.
953.
Muhammad Akhyar Farrukh Noureen Siraj Iftikhar Imam Naqvi 《Journal of Saudi Chemical Society》2010,14(2):209-212
Iron has been determined in apple and vegetables spectrophotometrically, by complexing it with xylenol orange. 1:1 complex formed in a highly acidic medium is measured for its absorbance at its λmax of 585 nm. The results have been compared by employing atomic absorption technique. Apples and vegetable samples were collected from local markets of Pakistan. Statistical manipulations, t-test and F-test, were performed and it was found that the results from the two techniques have an excellent agreement. 相似文献
954.
The expansion coefficient CD|L| of Coulomb potential 1/r12 of atomic system in hyper‐spherical harmonics is derived and the explicit expression is given. 相似文献
955.
956.
D. Raghavan X. Gu T. Nguyen M. Vanlandingham 《Journal of Polymer Science.Polymer Physics》2001,39(13):1460-1470
Characterization of polymer coatings microstructure is critical to the fundamental understanding of the corrosion of coated metals. An approach for mapping the chemical heterogeneity of a polymer system using chemical modification and tapping‐mode atomic force microscopy (TMAFM) is demonstrated. This approach is based on the selective degradation of one of the phases in a multiphase polymer blend system and the ability of TMAFM to provide nanoscale lateral information about the different phases in the polymer system. Films made of a 70:30 polyethyl acrylate/polystyrene (PEA/PS) blend were exposed to a hydrolytic acidic environment and analyzed using TMAFM. Pits were observed to form in the PEA/PS blend films, and this degradation behavior was similar to that of the PEA material. Using these results, the domains in the 70:30 blend were identified as the PS‐rich regions and the matrix as the PEA‐rich region. This conclusion was confirmed by Fourier transform infrared‐attenuated total reflection analyses that revealed the hydrolysis of the PEA material. TMAFM phase imaging was also used to follow pit growth of the blend as a function of exposure time. The usefulness of the chemical modification/AFM imaging approach in understanding the degradation process of a coating film is discussed. © 2001 John Wiley & Sons, Inc. J Polym Sci B Part B: Polym Phys 39: 1460–1470, 2001 相似文献
957.
The electrochemical behavior in alkaline solution (1 M NaOH) of nanocrystalline Ti:Ru:Fe:O (2:1:1:2) prepared by high-energy ball milling was studied over its whole electroactivity domain, with a particular emphasis on the hydrogen evolution reaction (her). Comparison has also been made with nanocrystalline Ti:Ru:Fe (2:1:1) and a mixture of Ti:TiO:Ru:Fe2O3 (3/2:1/2:1:1/2). It was shown by cyclic voltammetry, open circuit potential decay and chronopotentiometry measurements that hydrogen absorption in the electrode material occurs during hydrogen discharge. The electrochemical behavior of nanocrystalline Ti:Ru:Fe:O (2:1:1:2) closely follows that of Ti:Ru:Fe (2:1:1), but differs radically from that of Ti:TiO:Ru:Fe2O3 (3/2:1/2:1:1/2). This is due to the fact that the former two compounds contain a significant fraction of B2 phase (59 and 97 wt.%, respectively), while the latter does not. In steady state conditions, the ratio H/B2 phase in nanocrystalline Ti:Ru:Fe:O (2:1:1:2) is 0.15, about 1.6 times less than that for the O-free nanocrystalline compound. The coefficient of diffusion of hydrogen in nanocrystalline Ti:Ru:Fe:O (2:1:1:2) is 2.6×10−13 cm2 s−1, more than three times less than that in nanocrystalline Ti:Ru:Fe (2:1:1). The difference between the hydrogen absorption characteristics of both nanocrystalline compounds are tracked down to the fact that their B2 phases have different stoichiometries. 相似文献
958.
测量和减小纳米凹凸面摩擦力的分子新技术 总被引:1,自引:1,他引:0
报道了美国用原子力显微镜可直接检测超微型设备内发动机转子与外表表面上凸点之间摩擦力的大小的研究成果,介绍了降低了时机的摩擦力的方法。 相似文献
959.
Poly(ethylene glycol) (PEG) was modified with aniline groups at both the end, and then PEG‐PANI rod‐coil block polymers have been synthesized by polymerization of the aniline with the aniline‐modified PEG. FTIR, NMR, and elemental analysis provided the chemical strucutre of the as‐prepared polymers. The achiral rod‐coil copolymer could form different superstructures by means of self‐assembly when adding diethyl ether into its THF solution and the length of PANI segments is a key factor to the superstructures. AFM measurements revealed that they form spring‐like helical superstructures from the short PANI‐containing copolymers while these form fibrous helical superstructures from the longer PANI‐containing copolymer. A possible mechanism of the helical superstructures is suggested in this article and the driving force is believed the π–π stacking of the rigid segment of the copolymers. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 12–20, 2008 相似文献
960.
B. Witzel N.A. Papadogiannis D. Charalambidis 《The European Physical Journal D - Atomic, Molecular, Optical and Plasma Physics》2000,12(1):21-25
A new device for charged particle coincidence experiments in strong-field, short pulse laser-atom/molecule interactions is
presented. The device consists of a single time of flight spectrometer, common for both positive and negative charge detection.
Experimental parameters required for the use of the device in the high intensity regime are discussed. A demonstration of
electron-ion coincidence measurements in the interaction of Xe atoms with 60 fs laser pulses at 800 nm and an intensity of
W/cm2 is reported.
Received 22 November 1999 相似文献