Fourier transform surface studies

Fourier Transform IR Studies of Surface Adsorbates and Surface-Mediated Reactions... 

In Situ Surface Fourier Transform Infrared Study of Adsorption of Isoquinoline at a Mercury Electrode... 

Tolbert, M. A., and A. M. Middlebrook, Fourier Transform Infrared Studies of Model Polar Stratospheric Cloud Surfaces Growth and... 

Tolbert, M.A., and Middlebrook, A.M. (1990) Fourier Transform infrared studies of model polar stratospheric cold surfaces growth and evaporation of ice and nitric acid/ice, J. Geophys. Res. 95, 22423-22431. 

Recent advances in the development of non-invasive, in situ spectroscopic scanned-probe and microscopy techniques have been applied successfully to study mineral particles in aqueous suspension (Hawthorne, 1988 Hochella and White, 1990). In situ spectroscopic methods often utilise molecular probes that have diagnostic properties sensitive to changes in short-range molecular environments. At the particle-solution interface, the molecular environment around a probe species is perturbed, and the diagnostic properties of the probe, which can be either optical or magnetic, then report back on surface molecular structure. Examples of in situ probe approaches that have been used fruitfully include electron spin resonance (ESR) and nuclear magnetic resonance (NMR) spin-probe studies perturbed vibrational probe (Raman and Fourier-transform IR) studies and X-ray absorption (Hawthorne, 1988 Hochella and White, 1990 Charletand Manceau, 1993 Johnston et al., 1993). 

Johnson, B.B., Sjoberg, S., and Persson, P, Surface complexation of mellitic acid to goethite An attenuated total reflection Fourier transform infrared study, Langmuir, 20, 823, 2004. 

The association of several techniques to study the same system is always advantageous. For the specific case of surfaces, techniques like XPS, contact angle, diffuse reflectance infrared with Fourier transform, surface area and pore size measurements, scanning electron microscopy appear frequently associated. This is the case for the study of carbon or glass fibers [ 105-109], activated carbons [110], and polymeric films obtained by plasma polymerization [111]. In Section 5, the specific combination of diffuse reflectance spectroscopies in the region of UVA is and XPS will be emphasized. 

The adsorption of NAD+ on Au has been further studied during recent years using fourier transform surface-enhanced Raman scattering (FT-SERS) [113-115]. The surface-enhanced Raman scattering (SERS) of NAD+ shows a strong potential dependence in the non-Faradaic regions. Either the adenine or the nicotinamide... 

Xu, X.D., Mol, J.C., andBoelhouwer, C. Surface acidity of some Rc207-containing metathesis catalysts — An in situ Fourier Transform infrared study using pyridine adsorption. J. Chem. Soc., Faraday Trans. 1 1986, 82, 2707-2718. 

Chafik T, Kameoka S, Ukisu Y, et al. In situ diffuse reflectance infrared Fourier transform spectroscopy study of surface species involved in NOx reduction by ethanol over alumina supported silver catalyst. J Mol Catal A Chem. 1998 136 203-11. 

Transmission Fourier Transform Infrared Spectroscopy. The most straightforward method for the acquisition of in spectra of surface layers is standard transmission spectroscopy (35,36). This approach can only be used for samples which are partially in transparent or which can be diluted with an in transparent medium such as KBr and pressed into a transmissive pellet. The extent to which the in spectral region (typically ca 600 4000 cm ) is available for study depends on the in absorption characteristics of the soHd support material. Transmission ftir spectroscopy is most often used to study surface species on metal oxides. These soHds leave reasonably large spectral windows within which the spectral behavior of the surface species can be viewed. 

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. 

Surface forces measurement is a unique tool for surface characterization. It can directly monitor the distance (D) dependence of surface properties, which is difficult to obtain by other techniques. One of the simplest examples is the case of the electric double-layer force. The repulsion observed between charged surfaces describes the counterion distribution in the vicinity of surfaces and is known as the electric double-layer force (repulsion). In a similar manner, we should be able to study various, more complex surface phenomena and obtain new insight into them. Indeed, based on observation by surface forces measurement and Fourier transform infrared (FTIR) spectroscopy, we have found the formation of a novel molecular architecture, an alcohol macrocluster, at the solid-liquid interface. 

At present, most workers hold a more realistic view of the promises and difficulties of work in electrocatalysis. Starting in the 1980s, new lines of research into the state of catalyst surfaces and into the adsorption of reactants and foreign species on these surfaces have been developed. Techniques have been developed that can be used for studies at the atomic and molecular level. These techniques include the tunneling microscope, versions of Fourier transform infrared spectroscopy and of photoelectron spectroscopy, differential electrochemical mass spectroscopy, and others. The broad application of these techniques has considerably improved our understanding of the mechanism of catalytic effects in electrochemical reactions. 

Diffuse Reflectance IR Fourier Transform Spectroscopy (DRIFTS) can be employed with high surface area catalytic samples that are not sufficiently transparent to be studied in transmission. In this technique, the diffusely scattered IR radiation from a sample is collected, refocussed, and analysed. Samples can be measured in the form of loose powders. 

These assumptions are partially different from those introduced in our previous model.10 In that work, in fact, in order to simplify the kinetic description, we assumed that all the steps involved in the formation of both the chain growth monomer CH2 and water (i.e., Equations 16.3 and 16.4a to 16.4e) were a series of irreversible and consecutive steps. Under this assumption, it was possible to describe the rate of the overall CO conversion process by means of a single rate equation. Nevertheless, from a physical point of view, this hypothesis implies that the surface concentration of the molecular adsorbed CO is nil, with the rate of formation of this species equal to the rate of consumption. However, recent in situ Fourier transform infrared (FT-IR) studies carried out on the same catalyst adopted in this work, at the typical reaction temperature and in an atmosphere composed by H2 and CO, revealed the presence of a significant amount of molecular CO adsorbed on the catalysts surface.17 For these reasons, in the present work, the hypothesis of the irreversible molecular CO adsorption has been removed. 

Microphonic Fourier transform infrared photoacoustic spectroscopy (FT-IR/PAS) has emerged as a useful tool for characterizing fractions of a monolayer of organic species adsorbed on opaque, high surface area samples. Such a study of calcined and sulfided hydrodesulfurization catalysts will be discussed. 

Spectroscopic techniques may provide the least ambiguous methods for verification of actual sorption mechanisms. Zeltner et al. (Chapter 8) have applied FTIR (Fourier Transform Infrared) spectroscopy and microcalorimetric titrations in a study of the adsorption of salicylic acid by goethite these techniques provide new information on the structure of organic acid complexes formed at the goethite-water interface. Ambe et al. (Chapter 19) present the results of an emission Mossbauer spectroscopic study of sorbed Co(II) and Sb(V). Although Mossbauer spectroscopy can only be used for a few chemical elements, the technique provides detailed information about the molecular bonding of sorbed species and may be used to differentiate between adsorption and surface precipitation. 

Titration calorimetry and cylindrical internal reflection-Fourier transform infrared (CIR-FTIR) spectroscopy are two techniques which have seldom been applied to study reactions at the solid-liquid interface. In this paper, we describe these two techniques and their application to the investigation of salicylate ion adsorption in aqueous goethite (a-FeOOH) suspensions from pH 4 to 7. Evidence suggests that salicylate adsorbs on goethite by forming a chelate structure in which each salicylate ion replaces two hydroxyls attached to a single iron atom at the surface. 

To put things into perspective, we. can broadly classify these analytical methods into bulk, dry surface, and in situ interfacial techniques. This chapter focuses on the last category, illustrating two in situ techniques used to study anion binding at the goethite (a-FeOOH)-water interface titration calorimetry and cylindrical internal reflection-Fourier transform infrared (CIR-FTIR) spectroscopy. In fact, CIR-FTIR could prove to be extremely powerful, since it allows direct spectroscopic observation of ions adsorbed at the mineral-water interface. 

Most earlier papers dealt with the mercury electrode because of its unique and convenient features, such as surface cleanness, smoothness, isotropic surface properties, and wide range of ideal polarizability. These properties are gener y uncharacteristic of solid metal electrodes, so the results of the sohd met electrolyte interface studies are not as explicit as they are for mercury and are often more controversial. This has been shown by Bockris and Jeng, who studied adsorption of 19 different organic compounds on polycrystaUine platinum electrodes in 0.0 IM HCl solution using a radiotracer method, eUipsometry, and Fourier Transform Infrared Spectroscopy. The authors have determined and discussed adsorption isotherms and the kinetics of adsorption of the studied compounds. Their results were later critically reviewed by Wieckowski. ... 

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