Transform infrared crystal

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... 

In situ Fourier transform infrared and in situ infrared reflection spectroscopies have been used to study the electrical double layer structure and adsorption of various species at low-index single-crystal faces of Au, Pt, and other electrodes.206"210 It has been shown that if the ions in the solution have vibrational bands, it is possible to relate their excess density to the experimentally observed surface. 

Faguy PW, Markovic N, Adzic RR, Fierro C, Yeager E. 1990. A study of bisulfate adsorption on Pt(lll) single crystal electrodes using in-situ Fourier transform infrared spectroscopy. J Electroanal Chem 289 245 -262. 

We have found new CO-tolerant catalysts by alloying Pt with a second, nonprecious, metal (Pt-Fe, Pt-Co, Pt-Ni, etc.) [Fujino, 1996 Watanabe et al., 1999 Igarashi et al., 2001]. In this section, we demonstrate the properties of these new alloy catalysts together with Pt-Ru alloy, based on voltammetric measurements, electrochemical quartz crystal microbalance (EQCM), electrochemical scanning tunneling microscopy (EC-STM), in situ Fourier transform infrared (FTIR) spectroscopy, and X-ray photoelectron spectroscopy (XPS). 

A rate enhancement effect due to secondary nucleation has been identified in the solution-mediated transformation of the 7-phase of (i)-glutamic acid to its / -phase [82]. In this study, the kinetics of the polymorphic transition were studied using optical microscopy combined with Fourier transform infrared, Raman, and ultraviolet absorption spectroscopies. The crystallization process of n-hexatriacontane was investigated using micro-IR methodology, where it was confirmed that single... 

The 11 nm-sized Ti02 were crystallized using either hydrothermal or thermal methods from 100 nm, amorphous gel spheres. The Ti02 crystal and agglomerate sizes were determined by X-ray diffraction (Philip 1080) and transmission electron microscopy (JEOL JEM 2010), respectively. The surface area and chemistry of the nanostructured Ti02 were analyzed by nitrogen physisorption (Coulter SA 3100) and Fourier transform infrared spectroscopy (FTIR, Perkin-Elmer GX 2000). Metal catalyst was deposited by incipient... 

The main techniques employed for the characterization of clusters include UV/vis optical absorption, luminescence, mass spectrometry, X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and Fourier transform infrared (FT-IR). Single crystal X-ray diffraction (XRD) has been used to determine the structures of a few clusters [17-19]. 

The monotonic increase of immobilized material vith the number of deposition cycles in the LbL technique is vhat allo vs control over film thickness on the nanometric scale. Eilm growth in LbL has been very well characterized by several complementary experimental techniques such as UV-visible spectroscopy [66, 67], quartz crystal microbalance (QCM) [68-70], X-ray [63] and neutron reflectometry [3], Fourier transform infrared spectroscopy (ETIR) [71], ellipsometry [68-70], cyclic voltammetry (CV) [67, 72], electrochemical impedance spectroscopy (EIS) [73], -potential [74] and so on. The complement of these techniques can be appreciated, for example, in the integrated charge in cyclic voltammetry experiments or the redox capacitance in EIS for redox PEMs The charge or redox capacitance is not necessarily that expected for the complete oxidation/reduction of all the redox-active groups that can be estimated by other techniques because of the experimental timescale and charge-transport limitations. 

While microscopic techniques like PFG NMR and QENS measure diffusion paths that are no longer than dimensions of individual crystallites, macroscopic measurements like zero length column (ZLC) and Fourrier Transform infrared (FTIR) cover beds of zeolite crystals [18, 23]. In the case of the popular ZLC technique, desorption rate is measured from a small sample (thin layer, placed between two porous sinter discs) of previously equilibrated adsorbent subjected to a step change in the partial pressure of the sorbate. The slope of the semi-log plot of sorbate concentration versus time under an inert carrier stream then gives D/R. Provided micropore resistance dominates all other mass transfer resistances, D becomes equal to intracrystalline diffusivity while R is the crystal radius. It has been reported that the presence of other mass transfer resistances have been the most common cause of the discrepancies among intracrystaUine diffusivities measured by various techniques [18]. 

Another similar study of crystallization was performed where on-line ATR-FTIR spectroscopy was used to provide concentration information, however on-line diffuse reflectance Fourier-transform infrared... 

Probing Metalloproteins Electronic absorption spectroscopy of copper proteins, 226, 1 electronic absorption spectroscopy of nonheme iron proteins, 226, 33 cobalt as probe and label of proteins, 226, 52 biochemical and spectroscopic probes of mercury(ii) coordination environments in proteins, 226, 71 low-temperature optical spectroscopy metalloprotein structure and dynamics, 226, 97 nanosecond transient absorption spectroscopy, 226, 119 nanosecond time-resolved absorption and polarization dichroism spectroscopies, 226, 147 real-time spectroscopic techniques for probing conformational dynamics of heme proteins, 226, 177 variable-temperature magnetic circular dichroism, 226, 199 linear dichroism, 226, 232 infrared spectroscopy, 226, 259 Fourier transform infrared spectroscopy, 226, 289 infrared circular dichroism, 226, 306 Raman and resonance Raman spectroscopy, 226, 319 protein structure from ultraviolet resonance Raman spectroscopy, 226, 374 single-crystal micro-Raman spectroscopy, 226, 397 nanosecond time-resolved resonance Raman spectroscopy, 226, 409 techniques for obtaining resonance Raman spectra of metalloproteins, 226, 431 Raman optical activity, 226, 470 surface-enhanced resonance Raman scattering, 226, 482 luminescence... 

Fourier transform infrared reflection-absorption spectroscopy studies (FTIR-RAS) by Tolbert and coworkers (Zondlo et al., 1998) of the uptake of HNO, on ice at 185 K have shown that a supercooled liquid forms on the surface upon evaporation of water, the ice film becomes more concentrated in HN03 and at stoichiometries of 3 1 and 2 1 H20 HN03, respectively, NAT and NAD crystallize out. The reactions of C10N02 and N2Os with the ice also led to the formation of supercooled H20-HN03 liquid layers on the ice surface. 

Fourier Transform Infrared Spectroscopy (FT-IR) measurements were made using a Nicolet Instruments 740 FT-IR spectrometer. A horizontal attenuated toted reflectance cell equipped with a 45° zinc-selenide crystal trough wets used. Spectra of neat solutions were obtained by co-addition of 256 scans at 4 cm- resolution. 

X-ray photoelectron spectroscopy (XPS) was used for elemental analysis of plasma-deposited polymer films. The photoelectron spectrometer (Physical Electronics, Model 548) was used with an X-ray source of Mg Ka (1253.6 eV). Fourier transform infrared (FTIR) spectra of plasma polymers deposited on the steel substrate were recorded on a Perkin-Elmer Model 1750 spectrophotometer using the attenuated total reflection (ATR) technique. The silane plasma-deposited steel sample was cut to match precisely the surface of the reflection element, which was a high refractive index KRS-5 crystal. 

The solid-state properties like crystallinity, polymorphism (crystal structure), shape (morphology), and particle size of drugs are important in the stability, dissolution, and processibility of drugs. Some commonly used methods in solid-state studies include microscopy, hot stage microscopy with polarized light, x-ray powder diffraction (XRPD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), Fourier transform infrared FTIR/Raman, and solid-state NMR. 

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