Characterization studies FTIR spectroscopy

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. 

Analytically, IR (FTIR) spectroscopy is unquestionably one of the most versatile techniques available for the measurement of molecular species in the laboratory today, and also for applications beyond the laboratory. A major benefit of the technique is that it may be used to study materials in almost any form, and usually without any modification all three physical states are addressed solids, liquids and gases. Also, it is a fundamental molecular property, and as such the information content can be considered to be absolute in terms of information content, and as such can be very diagnostic in terms of material purity and composition. Traces of impurities can be both uniquely detected and in most cases characterized. This is a very important attribute in a process analytical enviromnent. 

Manecki et al. (2000b) used the same three apatites to study both homogeneous and epitaxial heterogeneous nucleation. For this, AFM, SEM, optical microscopy, EDS, Fourier-transformed infrared (FTIR) spectroscopy, and XRD were used to characterize the apatites and the reaction... 

Studies of the adsorbed odCB phase by C NMR MAS and FTIR spectroscopies were carried out (ref.4). They evidence the occurence of protonated odCB species at the surface and their interaction with Bronsted sites of the catalyst. These features are confirmed by the very good application of the Hammett equation to the isomerisation of p-substituted bromobenzenes (Fig. la). This equation takes the form, log (rate) = constant + trp, in which charge transfer between the initial and the transition states is occuring, the use of cr+is prefered (ref. 16). 

In essence, the test battery should include XRPD to characterize crystallinity of excipients, moisture analysis to confirm crystallinity and hydration state of excipients, bulk density to ensure reproducibility in the blending process, and particle size distribution to ensure consistent mixing and compaction of powder blends. Often three-point PSD limits are needed for excipients. Also, morphic forms of excipients should be clearly specified and controlled as changes may impact powder flow and compactibility of blends. XRPD, DSC, SEM, and FTIR spectroscopy techniques may often be applied to characterize and control polymorphic and hydrate composition critical to the function of the excipients. Additionally, moisture sorption studies, Raman mapping, surface area analysis, particle size analysis, and KF analysis may show whether excipients possess the desired polymorphic state and whether significant amounts of amorphous components are present. Together, these studies will ensure lotto-lot consistency in the physical properties that assure flow, compaction, minimal segregation, and compunction ability of excipients used in low-dose formulations. 

The effects of substrate temperature (Ts b) on cubic boron nitride (c-BN) films synthesized using magnetron sputtering were studied. Fourier transform infrared (FTIR) spectroscopy. X-ray photoelectron spectroscopy (XPS) were employed to characterize the structure and composition of the films. It is found that Ts , plays a crucial role on the formation of cubic phase, and an appropriate T, , can lead to a high content. A tentative explanation on the mechanism of such Ts b effects is reported with the most details. 

In spite of many of the potential experimental pitfalls and difficulties (which should be viewed here as caveats rather than as deterrents), IR spectroscopy is still one of the simplest and most widely and routinely employed analytical tools in the study and characterization of polymorphs. Some other modifications, developments and hyphenated techniques are worthy of note here, since they often considerably enhance the potential of the technique while reducing the drawbacks. Perhaps the most obvious of these is the combination of microscopy with FTIR spectroscopy for visual examination and spectral characterization of small areas in heterogeneous samples or identity and analysis of the spatial distribution of components of mixtures (e.g. pharmaceutical formulations) (Messerschmidt and Harthcock 1988). 

The objective of this chapter is to show that particles in the mesoscopic regime have very different properties to the bulk phase and, specifically, to demonstrate how in-situ STM and FTIR spectroscopy have been successfully employed to determine information on the structure of model catalysts based on modification of substrate electrodes with metal particles of mesoscopic dimensions, and the effect of this structure on reactivity. It will be shown that studying these model electrodes helps provide a link between single-crystal electrodes, which have provided a wealth of useful information, and electrodes for real application. FTIR has long been invaluable as a probe for localized particle reaction on surfaces in electrochemical processes, and the present work will show how it can complement STM in providing excellent characterization of mesoscopic properties. 

Study of the modification of solid surfaces requires, preferably, surface sensitive methods. Spectroscopic techniques, for example X-ray photoelectron spectroscopy (XPS) and FTIR spectroscopy are excellent tools for gathering information on the chemical surface composition and the kind and number of functional surface groups. The fact that the carbon and nitrogen containing organic phase is only introduced during the adsorption procedure and locally fixed on the outside of the particles allows the use of established methods for polymer and solid-state characterization, particularly NMR and solid-state NMR spectroscopy (e.g. 13C CP MAS NMR). 

VIBRATIONAL SPECTROSCOPY Infrared and Raman spectroscopies have proven to be useful techniques for studying the interactions of ions with surfaces. Direct evidence for inner-sphere surface complex formation of metal and metalloid anions has come from vibrational spectroscopic characterization. Both Raman and Fourier transform infrared (FTIR) spectroscopies are capable of examining ion adsorption in wet systems. Chromate (Hsia et al., 1993) and arsenate (Hsia et al., 1994) were found to adsorb specifically on hydrous iron oxide using FTIR spectroscopy. Raman and FTIR spectroscopic studies of arsenic adsorption indicated inner-sphere surface complexes for arsenate and arsenite on amorphous iron oxide, inner-sphere and outer-sphere surface complexes for arsenite on amorphous iron oxide, and outer-sphere surface complexes for arsenite on amorphous aluminum oxide (Goldberg and Johnston, 2001). These surface configurations were used to constrain the surface complexes in application of the constant capacitance and triple layer models (Goldberg and Johnston, 2001). 

Metal oxide and hydroxide systems serve many functions, including roles as pigments, in mineralogy, and also in catalysis. The classic techniques used in such investigations have included diffraction (especially X-ray diffraction XRD), thermal analysis, transmission electron microscopy, Fourier transform infrared (FTIR) spectroscopy and Raman spectroscopy (see also Chapters 2 and 4). Until the introduction of voltammetry in the analysis of immobilized microparticles, electrochemical studies had been confined to solid electrolyte cells (Chapter 12), normally functioning at elevated temperatures. Unfortunately, these studies proved to be inapplicable for analytical characterization, and consequently a series of systematic studies was undertaken using immobilized microparticles of iron oxides and oxide-hydrates (for reviews, see... 

Investigations of the acidity of specific surface sites may be accomplished by studies coordinated with spectroscopic methods, such as infrared (JR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, or mass spectrometry (MS). Surface characterization with Fourier transform infrared (FTIR) spectroscopy can provide quantitative results with experimental methods that are easily performed. However, the transmission sampling techniques traditionally employed for infrared studies may introduce experimental artifacts on the analyzed surface (10,... 

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