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1.
H. Dhaouadi H. Marouani M. Rzaigui A. Madani 《Phosphorus, sulfur, and silicon and the related elements》2013,188(8):1801-1814
Chemical preparation, crystal structure, thermogravimetric and differential analysis, solid state 31P MAS NMR characterization, and IR spectroscopic investigations are given for a new organic cation dihydrogenmonophosphate, (2-CH3OC6H4CH2NH3)H2PO4. This compound is monoclinic C2/c, with unit cell parameters a = 27.740(8), b = 4.827(2), c = 16.435(3) Å, β = 93.79(2)°, V = 2196 (1) Å3, Z = 8, and ρ = 1.422 g · cm?3. The crystal structure has been determined and refined to R = 0.046 (Rw = 0.056), using 1,746 independent reflections with I > 3σ (I). Its atomic arrangement can be described by infinite polyanions [H2PO4] n n ?, organized in ribbons alternating with organic cations. Strong hydrogen bonds connect the different components. Electrical conductivity measurements show that the [2-CH3OC6H4CH2NH3]H2PO4 has a low ionic conductivity value at 403 K. 相似文献
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Firas Awaja Michael Gilbert Minoo Naebe Georgina Kelly Bronwyn Fox Russell Brynolf Paul J. Pigram 《Polymer Degradation and Stability》2013
Thermoplastic polyolefin panels were treated with a flame, flame & water, and accelerated thermo molecular adhesion process (ATmaP) treatment. XPS, contact angle and adhesion test (pull off) results were acquired over a one year period to determine the changes in the elemental composition, surface energy and adhesion strength respectively over time. All surface-treated thermoplastic polyolefin samples showed a sharp decline in adhesion strength up to an ageing period totalling 6 months. The decline in adhesion strength was correlated with a decline in the nitrogen-containing constituents and C–O functional groups at the surface and a decline in surface energy for the flame & water-treated sample. There was no significant change in adhesion strength for all samples for ageing periods greater than 6 months. ATmaP-treated thermoplastic polyolefin outperformed the other two surface treatments in adhesion strength tests due to ATmaP retaining nitrogen-based functional groups (mainly nitrogen oxides) over the year long study. This retention of functionality allowed for a slower ageing process for ATmaP-treated surfaces in comparison to the other surface treatments. 相似文献
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Márton Balázs Firas Rassoul-Agha Timo Seppäläinen 《Communications in Mathematical Physics》2006,266(2):499-545
We study space-time fluctuations around a characteristic line for a one-dimensional interacting system known as the random average process. The state of this system is a real-valued function on the integers. New values of the function are created by averaging previous values with random weights. The fluctuations analyzed occur on the scale n 1/4, where n is the ratio of macroscopic and microscopic scales in the system. The limits of the fluctuations are described by a family of Gaussian processes. In cases of known product-form invariant distributions, this limit is a two-parameter process whose time marginals are fractional Brownian motions with Hurst parameter 1/4. Along the way we study the limits of quenched mean processes for a random walk in a space-time random environment. These limits also happen at scale n 1/4 and are described by certain Gaussian processes that we identify. In particular, when we look at a backward quenched mean process, the limit process is the solution of a stochastic heat equation. 相似文献
5.
Zhi Ping Xu Zi Gu Xiaoxi Cheng Firas Rasoul Andrew K. Whittaker Gao Qing Max Lu 《Journal of nanoparticle research》2011,13(3):1253-1264
A novel nanocomposite film for sustained release of anionic ophthalmic drugs through a double-control process has been examined
in this study. The film, made as a drug-loaded contact lens, consists principally of a polymer hydrogel of 2-hydroxyethyl
methacrylate (HEMA), in whose matrix MgAl-layered double hydroxide (MgAl-LDH) nanoparticles intercalated with the anionic
drug are well dispersed. Such nanocomposite films (hydrogel-LDH-drug) contained 0.6–0.8 mg of MgAl-LDH and 0.08–0.09 mg of
the ophthalmic drug (ketorolac) in 1.0 g of hydrogel. MgAl-drug-LDH nanoparticles were prepared with the hydrodynamic particle
size of 40–200 nm. TEM images show that these nanoparticles are evenly dispersed in the hydrogel matrix. In vitro release
tests of hydrogel-LDH-drug in pH 7.4 PBS solution at 32 °C indicate a sustained release profile of the loaded drug for 1 week.
The drug release undergoes a rapid initial burst and then a monotonically decreasing rate up to 168 h. The initial burst release
is determined by the film thickness and the polymerization conditions, but the following release rate is very similar, with
the effective diffusion coefficient being nearly constant (3.0 × 10−12 m2/s). The drug release from the films is mechanistically attributed to anionic exchange and the subsequent diffusion in the
hydrogel matrix. 相似文献
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Hydrolytic degradation of POSS-PEG-lactide hybrid hydrogels 总被引:2,自引:0,他引:2
A polyhedral oligomeric silsesquioxane (POSS), functionalized with eight arms of poly(ethylene glycol) (PEG; MW 400) and then acrylated, was incorporated into a hydrogel network based on triblock copolymers of poly(lactide-b-ethylene glycol-b-lactide) diacrylates using a redox-initiated polymerization. The organic-inorganic hybrid hydrogels so prepared contained the inorganic crosslinker POSS from 1 to 28 wt.%. The degradation properties of the hydrogels in a pH 7.4 phosphate-buffered saline solution at 37 °C were studied using measurements of mass loss, cryogenic SEM, and ATR-FTIR spectroscopy. It was found that copolymerization of acrylated 1kPEG-lactide with increasing amounts of POSS created a more porous network which was more resistant to hydrolysis. The ATR-FTIR technique was used to monitor the progress of degradation with exposure time through the changes in the carbonyl and C-H deformation bands of the lactide and the Si-C stretching band of the POSS. Increasing POSS incorporation resulted in decreased rate of degradation due to its hydrophobic nature and inertness to hydrolysis. Conversely, an increase in lactide content increased the degradation rate due to the increased number of hydrolytically-sensitive ester groups in the network. 相似文献
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Pellé F Dhaouadi M Michely L Aschehoug P Toncelli A Veronesi S Tonelli M 《Physical chemistry chemical physics : PCCP》2011,13(39):17453-17460
The synthesis and spectroscopic investigation of Pr(3+):YF(3) nanoparticles with nominal concentration between 0.05% and 5 at% Pr(3+) are reported. Pr(3+) emission in the visible range of the spectrum is investigated at room temperature and at 10 K as well as time resolved spectroscopy as a function of Pr(3+) concentration. The upconverted emission from the orange to the blue region is observed and the time-resolved spectroscopy of the visible emissions is discussed as a function of the doping level. A careful analysis of the decays permits identification of the main energy-transfer mechanisms that determine the population of the excited levels at various times during the decay. 相似文献
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We study the defocusing nonlinear Schrödinger (NLS) equation written in hydrodynamic form through the Madelung transform. From the mathematical point of view, the hydrodynamic form can be seen as the Euler–Lagrange equations for a Lagrangian submitted to a differential constraint corresponding to the mass conservation law. The dispersive nature of the NLS equation poses some major numerical challenges. The idea is to introduce a two‐parameter family of extended Lagrangians, depending on a greater number of variables, whose Euler–Lagrange equations are hyperbolic and accurately approximate NLS equation in a certain limit. The corresponding hyperbolic equations are studied and solved numerically using Godunov‐type methods. Comparison of exact and asymptotic solutions to the one‐dimensional cubic NLS equation (“gray” solitons and dispersive shocks) and the corresponding numerical solutions to the extended system was performed. A very good accuracy of such a hyperbolic approximation was observed. 相似文献
10.
Hui Hui Lee-Wang Idriss Blakey Traian V. Chirila Hui Peng Firas Rasoul Andrew K. Whittaker Bronwin L. Dargaville 《Macromolecular Symposia》2010,296(1):229-232
The possibility of employing self-healing gels as potential artificial vitreous substitutes is being explored. Advancement of traditional synthetic hydrogels as vitreous substitutes is hindered by their fragmentation upon injection into the vitreous cavity leading ultimately to inflammation. Preliminary work involved developing first generation self-healing gels, using amphiphilic tri-block copolymers of poly(propylene glycol)-block-poly(ethylene glycol)-block-poly(propylene glycol) (PPG-PEG-PPG) as the building block. Eight linear self-healing gels are synthesized by tethering an ureidopyrimidinone system to synthetically modified PPG-PEG-PPG via the formation of a bis-urea as a linker. The reversible nature of the hydrogen bonds permits alteration of their physical properties by changing the environment, yet retaining desirable characteristics. Despite low solubility in water, these polymers demonstrated associating behaviour under the investigated conditions, which is encouraging. Future generations of self-healing gels should involve the selection of a more hydrophilic core and/or star-like polymers to facilitate gel formation and strengthen the network. 相似文献