X-ray absorption spectral studies on stoichiometric analysis of amphiphilic ruthenium (II) polypyridine complex on a poly(methyl methacrylate) film

2001 ◽  
Vol 113 (2-3) ◽  
pp. 193-197 ◽  
Author(s):  
Shuji Matsuo ◽  
Takashi Nakano ◽  
Sunao Yamada ◽  
Taku Matsuo ◽  
Hisanobu Wakita
2014 ◽  
Vol 47 (1) ◽  
pp. 476-481 ◽  
Author(s):  
Keisuke Shimokita ◽  
Tsukasa Miyazaki ◽  
Hiroki Ogawa ◽  
Katsuhiro Yamamoto

A system for the simultaneous measurement of small-angle X-ray scattering and wide-angle X-ray diffraction (SAXS–WAXD) and the thickness of a coating film, obtained with an automatic coater, during film formation has been developed. The system was installed on beamline BL03XU at SPring-8. As model specimens, poly(methyl methacrylate)-b-poly(n-butyl acrylate)-b-poly(methyl methacrylate) (PMMA-b-PnBA-b-PMMA) triblock copolymers with different compositions were used to investigate the film formation process during solvent evaporation. First of all, the data correction methods were examined for the coating films during solvent evaporation. Since the scattering invariant was affected by the scattering volume and the absorption of X-rays by the solvent and the copolymer during drying, the scattering invariant should be corrected for the film width and the X-ray absorption of the sample. The polymer concentration was estimated from the thickness of the coating film during solvent evaporation, while the X-ray absorption was evaluated by using the X-ray linear absorption coefficients of the solvent and the copolymer. The results showed that the correction of the scattering invariant is crucial for an exact description of the film formation process during solvent evaporation.


2009 ◽  
Vol 79-82 ◽  
pp. 353-356
Author(s):  
Wei Pan ◽  
Yan Chen ◽  
Xiao Wei He

The polyacrylonitrile(PAN)/poly (methyl methacrylate)(PMMA) blend fibers were prepared by wet-spinning technique and carbonized over the temperature range of 400-1000°C in nitrogen atmosphere. After carbonization of the blend fibers, the PMMA component removed and the PAN component left in the form of carbon nanofibers. Morphology of the carbon nanofibers were investigated via scanning electron microscopy (SEM), and the carbonization behavior of the fibers were examined via x-ray diffraction (XRD), Raman microspectrometry. The optimal condition made carbon fibers with great L/D ratio and diameter less than 200 nm. XRD and Raman spectra shows that the PAN/PMMA blend fibers treated at 600°C produced some graphite crystallite.


2019 ◽  
Author(s):  
Jitendra Bahadur ◽  
S. K. Sharma ◽  
Avik Das ◽  
Debasis Sen ◽  
P. K. Pujari

Langmuir ◽  
2005 ◽  
Vol 21 (1) ◽  
pp. 437-442 ◽  
Author(s):  
Ferdi Karadas ◽  
Gulay Ertas ◽  
Eda Ozkaraoglu ◽  
Sefik Suzer

Polymer ◽  
1999 ◽  
Vol 40 (12) ◽  
pp. 3345-3351 ◽  
Author(s):  
Sebastien Urbanek ◽  
Kohji Tashiro ◽  
Tatsuki Kitayama ◽  
Koichi Hatada

2008 ◽  
Vol 41 (6) ◽  
pp. 985-990 ◽  
Author(s):  
P. Riello ◽  
M. Munarin ◽  
S. Silvestrini ◽  
E. Moretti ◽  
L. Storaro

Quantification of individual phases within a multiphase amorphous material has been achieved using a newly developed technique based on X-ray powder diffraction. The quantification method was developed during a study of an amorphous silica–poly(methyl methacrylate) (SiO2–PMMA) hybrid nanocomposite. The efficiency of the method as a quantifying tool for individual phases was demonstrated for samples of SiO2–PMMA prepared either by polymerization of methyl methacrylate in the presence of amorphous SiO2or by mechanically mixing known quantities of the individual and pre-prepared SiO2and PMMA materials. The weight percentages of amorphous SiO2in the nanocomposites as determined by application of the new technique were analogously found to be 29%, a result that was supported by thermogravimetric analysis and helium picnometry measurements.


1992 ◽  
Vol 30 (2) ◽  
pp. 185-195 ◽  
Author(s):  
B. W. Yates ◽  
D. M. Shinozaki ◽  
Ashok Kumar ◽  
William J. Meath

2018 ◽  
Vol 75 (6) ◽  
pp. 564-569 ◽  
Author(s):  
Sebastian Balos ◽  
Branka Pilic ◽  
Djordje Petrovic ◽  
Branislava Petronijevic ◽  
Ivan Sarcev

Background/Aim. Autopolymerized, or cold polymerized poly(methyl methacrylate) class of materials have a lower mechanical properties compared to hot polymerized poly(methyl methacrylate), due to a limited time of mixing before the polymerization process begins. The aim of this study was to test the effect of different relatively low nanosilica contents, in improving mechanical properties of the cold polymerized poly(methyl methacrylate). Methods. A commercially available autopolymerized poly(methyl methacrylate) denture reline resin methyl methacrylate liquid component was mixed with 7 nm after treated hydrophobic fumed silica and subsequently mixed with poly(methyl methacrylate) powder. Three nanosilica loadings were used: 0.05%, 0.2% and 1.5%. Flexural modulus and strength were tested, with one way ANOVA followed by Tukey?s test. Furthermore, zeta potential, differential scanning calorimetry, scaning electrone microscopy and energy dispersive X-ray analyses were performed. Results. Flexural modulus and strength of poly(methyl methacrylate) based nanocomposites were statistically significantly increased by the addition of 0.05% nano-SiO2. The increase in nanosilica content up to 1.5% does not contribute to mechanical properties tested, but quite contrary. The main reason was agglomeration, that occurred before mixing of the liquid and powder component and was proved by zeta potential measurement, and after mixing, proved by scanning electrone microscopy and energy dispersive x-ray analyses. Conclusions. Addition of 7 nm 0.05% SiO2 is the most effective in increasing flexural modulus and strength of autopolimerized poly(methyl methacrylate).


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