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101.
Saeed Ahmadi Vaselabadi David Shakarisaz Paul Ruchhoeft Joseph Strzalka Gila E. Stein 《Journal of Polymer Science.Polymer Physics》2016,54(11):1074-1086
Grazing‐incidence X‐ray scattering (GIXS) is widely used to analyze the crystallinity and nanoscale structure in thin polymer films. However, ionizing radiation will generate free radicals that initiate crosslinking and/or chain scission, and structural damage will impact the ordering kinetics, thermodynamics, and crystallinity in many polymers. We report a simple methodology to screen for beam damage that is based on lithographic principles: films are exposed to patterns of X‐ray radiation, and changes in polymer structure are revealed by immersing the film in a solvent that dissolves the shortest chains. The experiments are implemented with high throughput using the standard beam line instrumentation and a typical GIXS configuration. The extent of damage (at a fixed radiation dose) depends on a range of intrinsic material properties and experimental variables, including the polymer chemistry and molecular weight, exposure environment, film thickness, and angle of incidence. The solubility switch for common polymers is detected within 10–60 s at ambient temperature, and we verified that this first indication of damage corresponds with the onset of network formation in glassy polystyrene and a loss of crystallinity in polyalkylthiophenes. Therefore, grazing‐incidence X‐ray “patterning” offers an efficient approach to determine the appropriate data acquisition times for any GIXS experiment. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 1074–1086 相似文献
102.
103.
A simple, specific, and precise high-performance liquid chromatographic method has been developed for the simultaneous determination of ofloxacin (OFX), tetrahydrozoline hydrochloride (THC), and prednisolone acetate (PAC) in ophthalmic suspension using propylparaben (POP) as the internal standard. The mobile phase consists of 0.05 M phosphate buffer-acetonitrile (65:35, v/v), and the pH is adjusted to 2.7 with orthophosphoric acid. A column containing octadecyl silane chemically bonded to porous silica particles (Waters Spherisorb, 5 microm ODS 1, 4.6 x 150 mm) is used as the stationary phase. The detection is carried out using a variable wavelength UV-vis detector set at 210 nm for OFX and THC and 254 nm for POP (internal standard) and PAC. The solutions are chromatographed at a constant flow rate of 1.2 mL/min. Retention times for OFX, THC, POP, and PAC are approximately 2.5, 4.5, 7.8, and 9.5 min, respectively. The relative retention times are approximately 0.14 min for OFX, 0.35 min for THC, 1.00 min for POP, and 1.22 min for PAC. The linearity range and percent recoveries for OFX, THC, and PAC are 24-120, 4-16, and 16-80 microg/mL and 100.48%, 100.34%, and 100.21%, respectively. 相似文献
104.
Saeed?Rastegar Naser?MohammadiEmail author Reza?Bagheri 《Colloid and polymer science》2004,283(2):145-153
The morphology of a quaternary blend containing a diglycidyl ether of bisphenol-A (DGEBA), a thermoplastic modifier (PMMA), a phase-separating curing agent (diaminodiphenylmethane, DDM), and a non-phase-separating curing agent (methylenebis(3-chloro-2,6-diethylaniline, MCDEA) was studied as a function of volume fraction of the thermoplastic modifier and fractional concentration of the curing agents in their mixture. It was found that using mixtures of curing agents a co-continuous morphology could be obtained at PMMA concentrations as low as 2.5 volume percent. Using FTIR spectroscopy it was proved that specific interactions are present between PMMA and individual amine curing agents. On the other hand, there was no detectable specific interaction between PMMA and DGEBA. By analyzing the micro-indentation hardness data of the cryo-fractured samples and putting forward the intrinsic hardness concept, it was proposed that the co-continuous morphology is inherently more effective than the other morphologies in changing the mechanical properties of the above-mentioned multi-component blends. 相似文献
105.
Qian W Chuang SC Amador RB Jarrosson T Sander M Pieniazek S Khan SI Rubin Y 《Journal of the American Chemical Society》2003,125(8):2066-2067
A rational synthetic approach to the first four-membered ring-containing derivatives of C(62) is reported. They were synthesized by an inverse electron demand Diels-Alder reaction of 3,6-diaryl-1,2,4,5-tetrazines with C(60) in o-dichlorobenzene, followed by visible light irradiation at reflux. The structure of these nonclassical fullerenes derivatives was determined by X-ray single-crystal diffraction. 相似文献
106.
107.
Jahan B. Ghasemi Shabnam Hooshmand Saeed Rayati 《Journal of inclusion phenomena and macrocyclic chemistry》2013,76(1-2):47-54
A novel, fast and easy single sample measurement has been developed based upon temperature dependence of equilibrium constant in order to determine the enthalpy and entropy changes of a complexation reaction using spectrophotometric temperature titration. The method can be used in determination of the formation constant and thermodynamic parameters of the solutions that there are difficulties in their titration where volatile compounds are studying. Knowledge of component spectra is not required for the analysis. The formation constants of the interactions of ß-di and tri-brominated meso-tetraphenylporphyrins, and meso-tetrakis(4-methylphenyl) and (4-methoxyphenyl) porphyrins with Me2SnCl2 and Bu2SnCl2, have been determined in range of 0–25 °C utilizing van’t Hoff relation, mass balance and equilibrium constant equations by an iterative least squares method with ΔH 0 as adjustable parameter. The outputs of analysis are the equilibrium constants, ligand and adduct spectral profiles, their concentrations as a function of temperature, the adjusted values of the standard enthalpy ΔH 0, and entropy ΔS 0 changes. The order of formation constants of the resulting 1:1 complexes decreased with increasing number of bromide substituents and increased with adding methyl and methoxy groups, and vary as H2T(4-CH3O)PP > H2T(4-CH3)PP > H2TPP > H2TPPBr2 > H2TPPBr3 and Me2SnCl2 > Bu2SnCl2. 相似文献
108.
Dariush Rostamifard Mehdi Fallahnezhad Salman Zaferanlouei Saeed Setayeshi Mohammad Hassan Moradi 《Heat and Mass Transfer》2011,47(4):439-448
A hybrid high order neural network (HHONN) and a feed forward neural network (FNN) are developed and applied to find an optimized
empirical correlation for prediction of dryout (DO) heat transfer. The values predicted by the HHONN and FNN models are compared
with each other and also with the previous values of empirical correlation. HONN successfully provides an efficient open-box
model of nonlinear input–output mapping which provides easier understanding of data mining. By removing the hidden layers,
HONN structures become simpler than FNNs and initialization of learning parameters (weights) will not be catastrophic. The
RMS results show that the HHONN model has superior fitting specification for prediction of DO heat transfer problem compared
to the other prediction methods. 相似文献
109.
The rates of hydrolysis of some pyridilmonoimines have been investigated in aqueous methanol medium of acetate buffer. The hydrolysis of the studied bases found to be slower than that of benzylideneaniline. It is evident from the dependent of the rate constants upon the buffer concentration that the rate equation has the form of special and general acid catalysis. From the results it is suggested that the rate-determining step appears to be the protonation of the nitrogen atom of the imino group of the monoamines at the employed pH. 相似文献
110.
Bahram Hemmateenejad Saeed Yousefinejad 《Analytical and bioanalytical chemistry》2009,394(7):1965-1975
This article describes the use of the net analyte signal (NAS) concept and rank annihilation factor analysis (RAFA) for building
two different multivariate standard addition models called “SANAS” and “SARAF.” In the former, by the definition of a new
subspace, the NAS vector of the analyte of interest in an unknown sample as well as the NAS vectors of samples spiked with
various amounts of the standard solutions are calculated and then their Euclidean norms are plotted against the concentration
of added standard. In this way, a simple linear standard addition graph similar to that in univariate calibration is obtained,
from which the concentration of the analyte in the unknown sample and the analytical figures of merit are readily calculated.
In the SARAF method, the concentration of the analyte in the unknown sample is varied iteratively until the contribution of
the analyte in the response data matrix is completely annihilated. The proposed methods were evaluated by analyzing simulated
absorbance data as well as by the analysis of two indicators in synthetic matrices as experimental data. The resultant predicted
concentrations of unknown samples showed that the SANAS and SARAF methods both produced accurate results with relative errors
of prediction lower than 5% in most cases. 相似文献