Determination of Radiation Damage in Isotactic Poly(methyl methacrylate) by X-ray Diffraction

1978 ◽  
Vol 11 (5) ◽  
pp. 1051-1053 ◽  
Author(s):  
R. P. Kusy ◽  
A. R. Greenberg
Keyword(s):  
Methyl Methacrylate ◽  
Radiation Damage ◽  
X Ray Diffraction ◽  
X Ray ◽  
Poly Methyl Methacrylate

Properties of Carbon Nanofibers Prepared from Polyacrylonitrile/Poly(methyl Methacrylate) Blend

2009 ◽  
Vol 79-82 ◽  
pp. 353-356
Author(s):  
Wei Pan ◽  
Yan Chen ◽  
Xiao Wei He
Keyword(s):  
Methyl Methacrylate ◽  
Carbon Nanofibers ◽  
Carbon Fibers ◽  
Nitrogen Atmosphere ◽  
Wet Spinning ◽  
X Ray Diffraction ◽  
X Ray ◽  
Poly Methyl Methacrylate ◽  
Graphite Crystallite ◽  
Raman Microspectrometry

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.

scholarly journals Preparation and Characterization of Zinc Oxide (Zno)/Polymethyl Methacrylate (PMMA) Nanocomposites

2021 ◽  
Vol 04 (04) ◽  
Author(s):  
Jayashree Bagawade ◽  
Keyword(s):  
Zinc Oxide ◽  
Methyl Methacrylate ◽  
Zinc Oxide Nanoparticles ◽  
Nanocomposite Films ◽  
Oxide Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Poly Methyl Methacrylate ◽  
Absorption Measurements

A series of novel zinc oxide / Poly (methyl methacrylate) nanocomposite films with different ZnO contents were prepared through inclusion of pre-synthesized zinc oxide nanoparticles. The physical composition and morphology of the as-prepared nanocomposites were studied by XRD and TEM. The TEM analyses revealed that the zinc oxide nanoparticles have a particle size of ~3–5 nm. X-ray diffraction proved the presence of the amorphous PMMA in the nanocomposites. The intermolecular interactions within the polymer nanocomposites were explored by FTIR and XRD. FTIR spectra confirmed the dispersion of the zinc oxide nanoparticles in the Poly (methyl methacrylate) i.e. PMMA matrices. The UV-Vis absorption measurements of the ZnO/PMMA nanocomposites proved their potential optical properties.

Sem and X-Ray Analysis of Renal and Biliary Calculi

1976 ◽  
Vol 34 ◽  
pp. 306-307
Author(s):  
R. J. Narconis ◽  
G. L. Johnson
Keyword(s):  
Chemical Constituents ◽  
Natural State ◽  
X Ray Diffraction ◽  
Chemical Methods ◽  
X Ray ◽  
Additional Dimension ◽  
Biliary Calculi ◽  
Calculus Formation ◽  
Scanning Electron

Analysis of the constituents of renal and biliary calculi may be of help in the management of patients with calculous disease. Several methods of analysis are available for identifying these constituents. Most common are chemical methods, optical crystallography, x-ray diffraction, and infrared spectroscopy. The application of a SEM with x-ray analysis capabilities should be considered as an additional alternative.A scanning electron microscope equipped with an x-ray “mapping” attachment offers an additional dimension in its ability to locate elemental constituents geographically, and thus, provide a clue in determination of possible metabolic etiology in calculus formation. The ability of this method to give an undisturbed view of adjacent layers of elements in their natural state is of advantage in determining the sequence of formation of subsequent layers of chemical constituents.

New Coordination Compounds of Fe(III) with Organic Ligands

2009 ◽  
Vol 59 (12) ◽  
Author(s):  
Mihaela Flondor ◽  
Ioan Rosca ◽  
Doina Sibiescu ◽  
Mihaela-Aurelia Vizitiu ◽  
Daniel-Mircea Sutiman ◽  
...  
Keyword(s):  
Chemical Analysis ◽  
Complex Compounds ◽  
Organic Ligands ◽  
X Ray Diffraction ◽  
X Ray ◽  
Elemental Chemical Analysis ◽  
Structural Formulae ◽  
Paramagnetic Properties

In this paper the synthesis and the study of some complex compounds of Fe(III) with ligands derived from: 2-(4-chloro-phenylsulfanyl)-1-(2-hydroxy-3,5-diiodo-phenyl)-ethanone (HL1), 1-(3,5-dibromo-2-hydroxy-phenyl)-2-phenylsulfanyl-ethanone(HL2), and 2-(4-chloro-phenylsulfanyl)-1-(3,5-dibromo-2-hydroxy-phenyl)-ethanone (HL3) is presented. The characterization of these complexes is based on method as: the elemental chemical analysis, IR and ESR spectroscopy, M�ssbauer, the thermogravimetric analysis and X-ray diffraction. Study of the IR and chemical analysis has evidenced that the precipitates form are a complexes and the combination ratio of M:L is 1:2. The central atoms of Fe(III) presented paramagnetic properties and a octaedric hybridization. Starting from this precipitation reactions, a method for the gravimetric determination of Fe(III) with this organic ligands has been possible. Based on the experimental data on literature indications, the structural formulae of the complex compounds are assigned.

Crystal structure determination of the conformation of two bicyclo[3.3.1]nonan-ones

1985 ◽  
Vol 63 (6) ◽  
pp. 1166-1169 ◽  
Author(s):  
John F. Richardson ◽  
Ted S. Sorensen
Keyword(s):  
Crystal Structure ◽  
Direct Methods ◽  
Chair Conformation ◽  
Molecular Structures ◽  
Boat Conformation ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
Final Agreement

The molecular structures of exo-7-methylbicyclo[3.3.1]nonan-3-one, 3, and the endo-7-methyl isomer, 4, have been determined using X-ray-diffraction techniques. Compound 3 crystallizes in the space group [Formula: see text] with a = 15.115(1), c = 7.677(2) Å, and Z = 8 while 4 crystallizes in the space group P21 with a = 6.446(1), b = 7.831(1), c = 8.414(2) Å, β = 94.42(2)°, and Z = 2. The structures were solved by direct methods and refined to final agreement factors of R = 0.041 and R = 0.034 for 3 and 4 respectively. Compound 3 exists in a chair–chair conformation and there is no significant flattening of the chair rings. However, in 4, the non-ketone ring is forced into a boat conformation. These results are significant in interpreting what conformations may be present in the related sp2-hybridized carbocations.

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