Raman spectroscopy crystal microscopy

SSNMR spectroscopy. However, FTIR and Raman spectroscopy, thermal microscopy, variable-temperature x-ray diffractometry (VTXRD), and DSC may also be used to identify polymorphs. Solvates may be similarly characterized by the techniques mentioned above. In addition, the stoichiometric number of the solvent molecules in the crystal lattice of solvates may be determined by thermogravimetric analysis (TGA), gas chromatography, or, in the case of a hydrate, by Karl Fiseher titrimetry [37]. 

Methods to study crystallization of deformed elastomers include x-ray diffraction [207,208,263-265], optical birefringence [266,267], infrared or Raman spectroscopy, electron microscopy [268], dilatometry [269, 270], NMR [271], and mechanical measurements [193,262,272]. Strain-induced crystallization is manifested in the latter by both greater hysteresis (Fig. 23) and a longer time for stress decay (Fig. 24). However, the shape of the stress-strain curve during extension does not obviously reveal the onset of crystallization [207,208,262]. 

Film-forming chemical reactions and the chemical composition of the film formed on lithium in nonaqueous aprotic liquid electrolytes are reviewed by Dominey [7], SEI formation on carbon and graphite anodes in liquid electrolytes has been reviewed by Dahn et al. [8], In addition to the evolution of new systems, new techniques have recently been adapted to the study of the electrode surface and the chemical and physical properties of the SEI. The most important of these are X-ray photoelectron spectroscopy (XPS), SEM, X-ray diffraction (XRD), Raman spectroscopy, scanning tunneling microscopy (STM), energy-dispersive X-ray spectroscopy (EDS), FTIR, NMR, EPR, calorimetry, DSC, TGA, use of quartz-crystal microbalance (QCMB) and atomic force microscopy (AFM). 

QCMB RAM SBR SEI SEM SERS SFL SHE SLI SNIFTIRS quartz crystal microbalance rechargeable alkaline manganese dioxide-zinc styrene-butadiene rubber solid electrolyte interphase scanning electron microscopy surface enhanced Raman spectroscopy sulfolane-based electrolyte standard hydrogen electrode starter-light-ignition subtractively normalized interfacial Fourier transform infrared... 

A number of methods are available for the characterization and examination of SAMs as well as for the observation of the reactions with the immobilized biomolecules. Only some of these methods are mentioned briefly here. These include surface plasmon resonance (SPR) [46], quartz crystal microbalance (QCM) [47,48], ellipsometry [12,49], contact angle measurement [50], infrared spectroscopy (FT-IR) [51,52], Raman spectroscopy [53], scanning tunneling microscopy (STM) [54], atomic force microscopy (AFM) [55,56], sum frequency spectroscopy. X-ray photoelectron spectroscopy (XPS) [57, 58], surface acoustic wave and acoustic plate mode devices, confocal imaging and optical microscopy, low-angle X-ray reflectometry, electrochemical methods [59] and Raster electron microscopy [60]. 

In 2007, in a very exhaustive paper, Paradies and coworkers carried out a comprehensive structural characterization of the colorless and yellow forms of Af-hydroxyphthalimide (NHPI) by means of single-crystal X-ray diffraction, FTIR and Raman spectroscopies and scanning electron microscopy. In the yellow form, the Af-hydroxyl group is significantly out of the plane (1.19°), but the Af-hydroxyl group in the colorless form is only 0.06° out of the plane. The irreversible conversion of the colorless crystalhne form to the yellow crystalhne form is more like a dynamic isomerism than a polymorphic transformation. 

Crystal reaction study mechanistic tools, 296 computer simulation, 297 electronic spectroscopy, 298 electron microscopy, 298 electron paramagnetic resonance (EPR), 299 nuclear magnetic resonance (NMR), 298 Raman spectroscopy, 299 Crystal reaction study techniques crystal mounting, 308 decomposition limiting, 309 polarized IR spectroscopy, 309 temperature control, 308 Cycloreversions, adiabatic photochemical involving anthracenes, 203 excited state properties of lepidopterenes, 206... 

The application of novel in situ spectroscopic techniques for the study of Li electrodes in solutions should also be acknowledged. These include FTIR spectroscopy [108], atomic force microscopy (AFM) [109], electrochemical quartz crystal microbalance (EQCM) [110], Raman spectroscopy [111], and XRD [83],... 

Microstructural analysis of suspension plasma sprayed Ti02 coatings by Raman spectroscopy and transmission electron microscopy correlated well with results obtained by XRD. The anatase content in the coatings varied between 10 and 22 mass%, dependent on spraying parameters. Raman spectroscopy enabled the imaging of the spatial 2D-distribution of the rutile and anatase (Podlesak et al., 2008). Transmission electron microscope enabled to visualise the contact areas between the lamellae inside sprayed coatings as well as the columnar growth of crystal inside the lamellae. 

The potential of NIR FT-Raman spectroscopy for the investigation of zeolites (vanadyl-containing MFI, TS-1) as well as alumophosphate-based molecular sieves (AEI, CHA, CEO) are described. In Raman spectra of template containing samples bands of the organic species dominate. By dispersive Raman microscopy a spatial distribution in a CoAPO-34 crystal is observed. The Raman spectra allow a very rapid and sensitive detection of anatase formed during thermal treatment of as-synthesised titanium-containing zeolites. Different vanadium species are detected in vanadium-containing ZSM-5. 

Cellulose, which Is one of the most abundant organic substances found In nature, has been extensively studied by various techniques such as x-ray scattering, electron microscopy, IR and Raman spectroscopy, NMR spectroscopy etc. However, the crystal structure and noncrystalline state are not yet solved for cotton, ramie, bacterial and valonla celluloses which can be easily obtained in pure form. Cross-polarization/magic angle spinning(CP/MAS) C NMR spectroscopy is a promising new method to study these unsolved problems of cellulose, because this method is very sensitive to local molecular conformations and dynamics. 

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