Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

FTIR measurements

This approach finds experimental support in FTIR measurements of the oxidation of PANI in organic solvents which indicate an anion intercalation mechanism for the second oxidation step. However, the IR findings may also be interpreted as support for the formation of a protonated imine structure... [Pg.29]

This work was supported by National Research Foundation (NRF), South Africa, University of Zululand research committee and Walter Sisulu University (WSU) directorate of research. The authors thank Dr I. A Oluwafemi for technical assistance and Prof. Revaprasadu for the opportunity to work in his group. We also thank Manfred Scriba (CSIR) for TEM and HRTEM measurements and Ms V. Ncapayi for the FTIR measurements. [Pg.180]

Since spillover phenomena have been most directly sensed through the use of IR in OH-OD exchange [10] (in addition, in the case of reactions of solids, to phase modification), we used this technique to correlate with the catalytic results. One of the expected results of the action of Hjp is the enhancement of the number of Bronsted sites. FTIR analysis of adsorbed pyridine was then used to determine the relative amounts of the various kinds of acidic sites present. Isotopic exchange (OH-OD) experiments, followed by FTIR measurements, were used to obtain direct evidence of the spillover phenomena. This technique has already been successfully used for this purpose in other systems like Pt mixed or supported on silica, alumina or zeolites [10]. Conner et al. [11] and Roland et al. [12], employed FTIR to follow the deuterium spillover in systems where the source and the acceptor of Hjp were physically distinct phases, separated by a distance of several millimeters. In both cases, a gradient of deuterium concentration as a function of the distance to the source was observed and the zone where deuterium was detected extended with time. If spillover phenomena had not been involved, a gradientless exchange should have been observed. [Pg.98]

We express our thanks to Prof M.Yamada (Tohoku University) for the FTIR measurements and Mr. M.Matsuo (Rigaku Ltd.) for the XPS measurements. We are also grateful to Prof M.Nomura and staff of the Photon Factory, National Laboratory for High Energy Physics, for assistance in measuring EXAFS spectra (F oposals 89138 and 93G163). [Pg.512]

Coutanceau C, Hahn F, Waszczuk P, Wieckowski A, Lamy C, Leger J-M. 2002. Radioactive labeling study and FTIR measurements of methanol adsorption and oxidation on fuel cell catalysts. Fuel Cells 2 153-158. [Pg.456]

Several other reaction types on solid supports have also been investigated utilizing microwave heating. For instance, in an early report, Yu and coworkers monitored the addition of resin-bound amines to isocyanates employing on-bead FTIR measurements in order to investigate the differences in reaction progress under microwave heating and thermal conditions [63]. [Pg.332]

This result represents the first use of FTIR measurements to obtain information about the hydrogen evolution reaction on iron. It also represents one of the first uses of FTIR to study the mechanism of the electrode kinetic reaction (14). [Pg.359]

Govaerts et al. (2004) proposed a parallel /1-helix model for prion rods that is consistent in overall dimensions with their low-resolution EM studies of two-dimensional PrP 27-30 crystals (Wille et al, 2002). In this model, residues 89-174 form 4 coils, or complete helical turns (Jenkins and Pickersgill, 2001), of a left-handed, parallel /Hielix (Fig. 5B). The coils of one monomer are proposed to stack on the coils of another to form an extended triangular -structure. Three of these triangular units pack together to form the fibril (Fig. 5G and D). The G-terminal a-helices (a2 and a3) of monomeric PrP are proposed to retain their native structure in the fibril and pack around the outside of the trimer (Fig. 5G and D). The presence of these helices in the prion rods is consistent with antibody binding studies (Peretz et al, 1997), the presence of a disulfide bond (Turk et al, 1988), and FTIR measurements (Wille et al, 1996). [Pg.243]

FTIR measurements of as-synthesized porous silicon indicate an abundance of Si-H and Si-Hj bonds (with nearly identical absorption peaks), with the suggestion of small amounts of Si-Ht. From [5] we have the following bond dissociation energies ... [Pg.106]

Bulut, G. and Atak, S., 2002. Role of dixanthogen on pyrite flotation solubility, adsorption studies and E h. FTIR measurements. Minerals Metallurgical Processing, 19(2) 81-86 Cases, J. M., Kongolo, M., de Donato, P., Michot, L. and Eire, R., 1990. Interaction between firely ground galena and pyrite with potassium amylxanthate in relation to flotation, 2. Influence of grinding media at natural pH. Inter. J. Miner. Process, 30 35 - 67... [Pg.270]

To check the completion of the reaction in Scheme 12.6, the single bead FTIR measurement (Fig. 12.10) alone was not conclusive because there was no IR band from the starting resin (11) to monitor. Resin elemental analysis (Cl) of (11) could conclusively show if the reaction was complete. The accuracy and the reproducibility of the resin elemental analysis methods have been evaluated before [14]. [Pg.511]

F. Lewiner, J.P. Klein, F. Puel and G. Fevotte, On-hne ATR-FTIR measurement of supersaturation during solution crystallization processes. Calibrations and applications on three solute/solvent systems, Chem. Eng. Sci., 56, 2069-2084 (2001). [Pg.456]

The most recent advance in VCD instrumentation has been its adaptation to Fourier transform infrared (FTIR) measurement (23-25). The details of this technique involve a new method of FTIR measurement termed double-modulation FTIR spectroscopy. Thus spectra of very high quality and resolution have been obtained using a standard VCD modulator and detector, a glower source, and a commercially available FTIR spectrometer system. In fact an entire FTIR-VCD spectrometer can be assembled from a few commercially available components. It is found that the major advantages of resolution, throughput, and... [Pg.119]

Rh s(CO)iis they revealed the presence of an unidentified complex which was suggested to be the previously unknown species Rh4(a-CO)i2-The BTEM protocol is an extremely powerful technique to recover pure component spectra of unknown species, even when present at very low concentrations. This was illustrated by a detailed mechanistic study of the promoting effect of HMn(CO)5 on the Rh4(CO)i2 catalyzed hydroformylation of 3,3-dimethylbut-l-ene [22], A dramatic increase in the hydroformylation rate was found when both metals were used simultaneously. Detailed in situ FTIR measurements using the BTEM protocol indicated the presence of homometallic complexes only during catalysis. The metal complexes that were identified under catalytic conditions were RC(0)Rh(C0)4, Rh4(CO)i2, Rh5(CO)i5, HMn(CO)s, and Mn2(CO)io (see Figure 6.6). The kinetics of product formation showed an overall product formation rate, Eq. (3) ... [Pg.238]

Table 11.2 summarizes the detection limits for FTIR measurements in the atmosphere for some gases of interest. Typical concentrations of each in remote to polluted atmospheres are discussed below with respect to the individual species however, in general, it can be stated that FTIR is most suitable for measuring... [Pg.551]

Notholt, J., The Moon as a Light Source for FTIR Measurements of Stratospheric Trace Gases during the Polar Night Application for HNO, in the Arctic, J. Geophys. Res., 99, 3607-3614 (1994). [Pg.719]

Spectroscopic, that is, fluorescence and circular dichroism (CD), fourier transform infared (FTIR) measurements have been widely applied to analyzing changes in enzyme structures in an attempt to explain the stabilization or denaturation phenomena associated with enzyme environments, for example, temperature, solvents, and so on. All these measurements can also be performed in ILs where fluorescence and CD spectroscopy demonstrated the conformational changes in the native structure of calcium binding proteins (CALB) which resulted in the higher s)mthetic activity and stability in ILs as compared to those obtained in classical organic solvents [18].The stabilization of enzymes by ILs may be related to the associated structural changes of proteins [19]. [Pg.298]


See other pages where FTIR measurements is mentioned: [Pg.393]    [Pg.31]    [Pg.398]    [Pg.477]    [Pg.233]    [Pg.108]    [Pg.166]    [Pg.457]    [Pg.459]    [Pg.476]    [Pg.478]    [Pg.491]    [Pg.532]    [Pg.187]    [Pg.127]    [Pg.147]    [Pg.145]    [Pg.321]    [Pg.59]    [Pg.120]    [Pg.64]    [Pg.94]    [Pg.268]    [Pg.220]    [Pg.84]    [Pg.133]    [Pg.135]    [Pg.576]    [Pg.258]    [Pg.266]    [Pg.266]   


SEARCH



An example of a static (low temperature) FTIR measurement, the BR to K transition

FTIR spectroscopic measurements

FTIR-ATR Measurements

Micro-FTIR measurements

Reflection FTIR imaging measurements

© 2024 chempedia.info