HPLC systems

Typical HPLC system consists of the following main components [Pg.9]

Solvent Reservoirs. Storage of sufficient amount of HPLC solvents for continuous operation of the system. Could be equipped with an online degassing system and special filters to isolate the solvent from the influence of the environment. [Pg.9]

This provides the constant and continuous flow of the mobile phase through the system most modern pumps allow controlled mixing of different solvents from different reservoirs. [Pg.9]

Injector. This allows an introduction (injection) of the analytes mixture into the stream of the mobile phase before it enters the column most modern injectors are autosamplers, which allow programmed injections of different volumes of samples that are withdrawn from the vials in the autosampler tray. [Pg.9]

Column. This is the heart of HPLC system it actually produces a separation of the analytes in the mixture. A column is the place where the mobile phase is in contact with the stationary phase, forming an interface with enormous surface. Most of the chromatography development in recent years went toward the design of many different ways to enhance this interfacial contact (a detailed discussion is given in Chapter 3). [Pg.9]

HPLC system incorporating a postcolumn matrix-addition facility. Note the pump used for postcolumn addition must be essentially pulse free. [Pg.85]

The composition of PPG—PEG blends has been determined using gpc with coupled density and RI detectors. PEG and PPG have different response factors for the density and RI detectors which were exploited (173). An hplc system with CHROMPAC RP-18C2g column at 298°C and acetonitrile—water or methanol—water as the mobile phase has been used to gather information about the functionaUty of PPO (174). [Pg.354]

Coupling of analytical techniques (detectors) to high-performance liquid chromatographic (HPLC) systems has increased in the last tree decades. Initially, gas chromatography was coupled to mass spectrometry (MS), then to infrai ed (IR) spectroscopy. Following the main interest was to hyphenate analytical techniques to HPLC. [Pg.342]

HPLC systems coupled to mass spectrometers (LC-MS) are extremely important methods for the separation and identification of substances. If not for the costs involved in LC-MS, these systems would be more commonly found in research laboratories. [Pg.25]

P.C. Sadek, Troubleshooting HPLC Systems A Bench Manual, Wiley-Interscience, New York, 1999. ISBN 0471178349. [Pg.49]

Connect the column to the high-performance liquid chromatography (HPLC) system in the reverse flow direction. [Pg.135]

Connect the column to the HPLC system in the normal flow direction. [Pg.135]

A block diagram of an HPLC system, illustrating its major components, is shown in Figure 2.1. These components are discussed in detail below. [Pg.27]

Figure 2.1 Block diagram of a typical HPLC system.

Unlike gas chromatography, in which the mobile phase, i.e. the carrier gas, plays no part in the separation mechanism, in HPLC it is the relative interaction of an analyte with both the mobile and stationary phases that determines its retention characteristics. Hence, it is the varying degrees of interaction of different analytes with the mobile and stationary phases which determines whether or not they will be separated by a particular HPLC system. [Pg.29]

If the identity of the analyte is genuinely unknown, a farther problem is encountered. In contrast to GC, there are no HPLC systems, combinations of mobile and stationary phases, that are rontinely used for general analyses. Therefore, there are no large collections of k values that can be nsed. For this reason, retention characteristics are often nsed for identification after the nnmber of possible compounds to be considered has been greatly reduced in some way, e.g. the class of compound involved has been determined by colonr tests or UV spectroscopy. [Pg.39]

In this chapter, an HPLC system has been described in terms of its component parts and the effect of each of these on the use of a mass spectrometer as a detector... [Pg.47]

One of the major problems with this type of interface, not unsurprisingly, is clogging of the pinhole. For this reason, the HPLC system has to be kept scrupulously clean with solvents being passed through narrow filters to remove any solid particles and in-line filters being incorporated to ensure that column material does not find its way into the probe. [Pg.141]

In conventional FAB (see Section 3.2.3), the analyte is mixed with an appropriate matrix material and applied to the end of a probe where it is bombarded with a fast-atom, or latterly, a fast-ion, beam. There are two major considerations when linking HPLC to such a system, namely (a) how is the matrix material, which is crucial for effective ionization in conventional FAB, to be incorporated into the system, and (b) how is the flowing HPLC system to be continuously presented to the ionizing beam ... [Pg.144]

Two forms of interface have been commercially developed [7] which allow analytes in a flowing liquid stream - it has to be pointed out, not necessarily from an HPLC system (see below) - to be ionized by using FAB. These are essentially identical except for that part where the HPLC eluate is bombarded with the heavy-atom/ion beam. Both of these interfaces consist of a probe in the centre of which is a capillary which takes the flowing HPLC eluate. In the continuous-flow FAB interface (Figure 4.3), the column eluate emerges from the end of the capillary and spreads over the probe tip, while in the frit-FAB interface the capillary terminates in a porous frit onto which the atom/ion beam is directed. [Pg.144]

The selectivity (separation capability) of an HPLC system is dependent upon the combination of mobile and stationary phases. Since ions are being generated directly from the mobile phase by electrospray, its composition, including the identity and concentration of any buffer used, and its flow rate are important considerations. [Pg.159]

Chemical reduction of the antibody results iu the productiou of both light aud heavy chaius, with the heavy chaius showiug the differeut levels of glycosyla-tion that are of iuterest. The HPLC system used to separate the fight and heavy chains consisted of a Poros Rl/H 100 x 2.1 nun column maintained at 60°C. Gradient elution was used from 90% of a 2% acetic acid solution (solvent A) 10% acetonitrile/2-propanol (70 30 vol/vol) (solvent B) to 25% solvent A 75% solvent B over 30 min at a flow rate of 0.5 mimin. ... [Pg.202]

The HPLC system comprised a 75 ftm x 15 cm PepMap column with a linear gradient of acetonitrile/0.1% aqueous formic acid (5 to 50% acetonitrile over 45 min) at a flow rate of 250 nlmin . Positive-ion electrospray ionization was employed using a nanospray interface. MS-MS specna were acquired over the range m/z 40 to 2000 at a rate of 1 s per scan. [Pg.225]

A method has been reported for the quantification of five fungicides (shown in Figure 5.39) used to control post-harvest decay in citrus fruits to ensure that unacceptable levels of these are not present in fruit entering the food chain [26]. A survey of the literature showed that previously [27] APCl and electrospray ionization (ESI) had been compared for the analysis of ten pesticides, including two of the five of interest, i.e. carbendazim and thiabendazole, and since it was found that APCl was more sensitive for some of these and had direct flow rate compatibility with the HPLC system being used, APCl was chosen as the basis for method development. [Pg.246]

A method has been reported for the quantification of the DNA oxidation products, 8-hydroxy-2 -deoxyguanosine (8-OH-dG), 8-hydroxy-2 -deoxyadenosine (8-OH-dA), 5-hydroxymethyl-2-deoxyuridine (HMDU), thymidine glycol (TG) and 2-hydroxy-2 -deoxyadenosine (2-OH-dA) [37], The HPLC system employed consisted of a 2.0 X 250 mm Cig column and gradient elution from waterimethanol, (94 6) to (10 90) over 28 min, at a flow rate of 200 tilmin ... [Pg.279]

The HPLC system used consisted of a 30 x 2 mm Luna CN column with linear gradient elution employing two mobile phases A and B (A, 90% H2O 10% acetonitrile B, 10% H2O 90% acetonittile) with both phases containing 5 mM ammonium acetate and 0.2% formic acid. The hnear gradient commenced with 50 50 A B increasing to 100% B after 1 min of the analysis this composition was maintained for 1 min before returning to 50 50 A B after 4 min. Positive-ion ionspray (pneumatically assisted electrospray) was used to obtain mass spectra, with the spectrometer operating at a resolution of 5000. [Pg.284]

Normal-phase HPLC An HPLC system in which the mobile phase is less polar that the stationary phase. [Pg.309]

Summary Sheet for HPLC Since all 10 calibration results are very close to 100% and no trend is apparent, the HPLC system is regarded as being in control. ... [Pg.285]

HPLC Systems Employing Reversed Phase C,8 Columns for Separation of Carotenoids... [Pg.457]

The availability of HPLC systems coupled to photodiode array detectors allows for online spectral characterization of anthocyanins. [Pg.492]

Liquid chromatography was monitored by a Gilson HPLC system. [Pg.770]

Whilst for the analysis of plant material for cannabinoids both GC and HPLC are commonly used, in analytical procedures the employment of GC-based methods prevails for human forensic samples. Nonetheless, the usage of HPLC becomes more and more of interest in this field especially in combination with MS [115-120]. Besides the usage of deuterated samples as internal standards Fisher et al. [121] describe the use of a dibrominated THC-COOH (see 7.5). The usage of Thermospray-MS and electrochemical detection provide good performance and can replace the still-used conventional UV detector. Another advantage in the employment of HPLC rather than GC could be the integration of SPE cartridges, which are needed for sample preparation in the HPLC-system. [Pg.31]

Another variation of the preceding method is to apply HPLC to fractionate the cleaned-up aliphatic-aromatic fraction from flash colurim separation of soluble organic matter as it is performed in the Chevron laboratory, for example, as described in Reference 2. A Waters HPLC system equipped with a preparative Whatman Partisil 10 silica column (9.4 X 500 mm), a HPLC pump, and two detectors for separation monitoring (a UV and refractive index detector) are used, giving three fractions of aliphatic hydrocarbons, mono-, di-, and triaromatics and polar compounds. The hrst two fractions are eluted with hexane, whereas polar compounds are eluted with... [Pg.372]

Advances in understanding solute interachons in liquid-liquid systems in a nonequilibrium environment brought reversed-phase (RP)-HPLC into the forefront of lipophilicity determinahon. The development and manufacturing of rigid, reproducible and well-characterized stationary phases and columns, as well as the accessibility and high level of automation of modern HPLC systems, have made RP-HPLC the method of choice for many laboratories. [Pg.416]

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