LC/IR systems

Similar results have been reported for LC-IR systems... 

These are GC-IR (5), LC-IR (6), and diffuse reflectance (7). On-the-fly GC-IR systems are commercially available, and lower detection limits are being continually reported. While GC-IR may not replace GC/MS in residue and metabolism work, it can provide valuable data in these areas. On-the-fly LC-IR systems have been developed and are also commercially available. The major problem in these systems is the strong infrared absorbence of many common LC solvents. However, with proper selection of solvents and the development of LC conditions specifically designed for the LC-IR experiment, these problems may be overcome. Recent reports on diffuse reflectance measurements by FTIR indicate the technique may provide a method of examining formulated material or TLC spots with no sample preparation. While this technique is still in the development stage, it may become quite significant in the future. 

Johnson et al. [36] developed a rather unique extraction cell for an LC/IR system. They used the segmented flow of an aqueous effluent from a reversed phase system and separated the extraction solvent by means of a "hydrophobic" (dispersive) membrane. A diagram of their apparatus is shown in figure 32. There are two pumps, one provides the solvent for the chromatographic development, and the other the... 

Jansen [52] developed an on-line LC-IR system for the analysis of additives in polymer extracts. 

Since APCI and ESI interfaces operate at atmospheric pressure and do not depend upon vacuum pumps to remove solvent vapor, they are compatible with a wide range of HPLC flow rates. HPLC methods that have been developed using conventional detectors such as UV/VIS, IR, or fluorescence are usually transferable to LC/MS systems without adjustment. However, the solvent system should contain only volatile solvents, buffers, or ion-pair agents to reduce fouling of the mass spectrometer ion source. In the case of chlorophyll solvent systems, isocratic and gradient combinations of methanol, acetonitrile, water, acetone, and/or ethyl acetate have been used for APCI or ESI LC/MS. Unlike continuous-flow FAB/LSIMS, no sample matrix is necessary. 

The position of the carousel is controlled automatically and only three positions are actively used. In the first position the eluent is deposited on the potassium chloride, in the second position a stream of air is drawn through the potassium chloride to remove the solvent and in the third position the spectrum is taken. The use of the carousel containing potassium chloride powder certainly increased the sensitivity of the LC/IR combination, but the finite intervals of sample collection made the system unsuitable for modern high efficiency columns. Jino and Fujimoto [30,31] employed a potassium bromide plate as a transport system. The eluent from a small bore column (flow rate 5 pi/ min)... 

In general, tandem systems involving the combination of the liquid chromatograph in-line with the infrared spectrometer have not been very successful and most IR spectra of LC eluents are obtained by what are, in effect, off-line procedures, as in the example given above. The FTIR spectrometer, in its present form, demands too large a sample size and is too insensitive for successful in-line association with modem high-efficiency microbore LC columns. Fortunately, the demand for in-line production of IR spectra from LC eluents is not great and, in most cases, the off-line methods are quite satisfactory for the majority of LC/IR applications. 

In general, the situation with respect to LC/IR is very similar to that of LC/NMR. There is still inadequate sensitivity coupled with extensive peak dispersion in the interface systems so far described. Furthermore, whereas the LC/NMR combination can provide very valuable structure information for an eluted solute, in contrast the information provided from LC/IR is more limited. Nevertheless, interfaces with very significant improvement in both sensitivity and dispersion have been realized over the past few years. However, at present, IR spectra may well be more easily... 

The most common detectors in HPLC are ultraviolet, fluorescence, electrochemical detector and diffractometer. However, despite all improvements of these techniques it seems necessary to have a more selectivity and sensitivity detector for the purposes of the medical analysis. It should be therefore improvements to couple analytical techniques like infrared IR, MS, nuclear magnetic resonance (NMR), inductively coupled plasma-MS (ICP-MS) or biospecific detectors to the LC-system and many efforts have been made in this field. 

Wilson et al. [662-665] have described various prototype systems for total organic analysis devices. It has proved technically feasible to obtain UV, IR, NMR and MS spectra (together with atomic composition based on accurate mass determination) following RPLC separation. The fully integrated approach offers the benefit that one chromatographic run is required, thus ensuring that all of the spectrometers observe the same separation. Such multiple hyphenations might favour the analysis of complex mixtures for both confirmation of identity and structure determination (should this represent a cost-effective approach). Table 7.72 illustrates the main features of on-flow multiple LC hyphenation. 

FTIR in multiply hyphenated systems may be either off-line (with on-line collection of peaks) [666,667] or directly on-line [668,669]. Off-line techniques may be essential for minor components in a mixture, where long analysis times are required for FT-based techniques (NMR, IR), or where careful optimisation of the response is needed. In an early study a prototype configuration comprised SEC, a triple quadrupole mass spectrometer, off-line evaporative FTIR with splitting after UV detection see Scheme 7.12c [667]. Off-line IR spectroscopy (LC Transform ) provides good-quality spectra with no interferences from the mobile phase and the potential for very high sensitivity. Advanced approaches consist of an HPLC system incorporating a UV diode array, FTIR (using an ATR flow-cell to obtain on-flow IR spectra), NMR and ToF-MS. 

Both a pneumatic heated nozzle system [487] and an ultrasonic nozzle/vacuum system [699] have been described for removing the troublesome solvent in order to simplify IR analysis. The former system (LC Transform ) has been commercialised [700], and allows full use of the mid-IR spectral range by providing analyte films free from solvent interference. The evaporative... 

The electrogeneration of [(TPP)Co] from (TPP)Co, and the reaction of this species with CHjI can be followed by cyclic voltammetry as shown in Figures lc and Id. In the absence of any added reagent, there are two reversible reduction waves which occur at Ei/2 = 0.85 jind -1.86 V (see Figure lc). These are due to the formation of [(TPP)CoJ and [(TPP)Co]2-, where the second reduction has occurred at the porphyrin ir ring system. The first reduction of (TPP)Co is not reversible in the presence of CH3I, and occurs at Ep = -0.86 V (see Figure Id). A new reversible reduction also appears at Ej/2 = -1.39 V. This process is due to (TPP)Co(CHj) which is formed as shown by Equation 8. The formation of (TPP)Co(CHj) as the final product of the electrosynthesis was confirmed by spectroelectrochemical experiments which were carried out under the same experimental conditions(26). 

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