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Chromatography spectroscopy, techniques

Although the majority of studies focus on the solid state, many applications focus more or additionally on the volatile products arising from polymer degradation. Evolved gas analysis (EGA) from thermal analysers and pyrolysers by spectroscopic and coupled chromatography-spectroscopy techniques can be particularly important from a safety and hazard viewpoint, since data from such measurements can be used to predict toxic or polluting gases from fires, incinerators, etc. [Pg.389]

At this stage each spot on the gel may contain several proteins. The spot of interest is removed by cutting the gel and dissolving with an enzyme. Then the cleaved proteins are studied by using chromatography and mass spectroscopy techniques to determine the amino acids in the proteins and their sequences. The results are compared with database and the identities of proteins are revealed. [Pg.78]

The analytical chemist will choose the appropriate analytical technique (e.g., chromatography, spectroscopy, or titration) to satisfy the technical objective based upon his or her expertise and past experiences with similar analytical problems. Often, however, the analyte itself dictates the kind of analysis method to be used. For example, a residual volatile solvent would most probably be analyzed by gas chromatography (GC), while a residual catalyst, such as palladium, would best be analyzed by atomic absorption or emission spectroscopy. [Pg.142]

As an instrumental approach to conventional electrophoresis, capillary electrophoresis offers the capability of on-line detection, micropreparative operation and automation (6,8,45-47). In addition, the in tandem connection of capillary electrophoresis to other spectroscopy techniques, such as mass spectrometry, provides high information content on many components of the simple or complex peptide under study. For example, it has been possible to separate and characterize various dynorphins by capillary electrophoresis-mass spectrometry (33). Therefore, the combination of CE-mass spectrometry (CE-MS) provides a valuable analytical tool useful for the fast identification and structural characterization of peptides. Recently, it has been demonstrated that the use of atmospheric pressure ionization using Ion Spray Liquid Chromatography/ Mass Spectrometry is well suited for CE/MS (48). This approach to CE/MS provides a very effective and straightforward method which allow the feasibility of obtaining CE/MS data for peptides from actual biological extracts, i.e., analysis of neuropeptides from equine cerebral spinal fluid (33). [Pg.7]

Research on betalains has received a significant impetus from recent developments in chromatography, spectroscopy, biochemistry and techniques of molecular biology. This has led to a rapid increase in our knowledge about new structures as well as key steps in their bios)mthesis. Some new structural features of betalains from plants are reviewed below, resulting primarily from advances in work on their bios)mthesis, whilst still being aware of the validity of earlier h3q)otheses. [Pg.67]

Whilst spectroscopy techniques can be used on their own to obtain spectral information about a sample they are also commonly incorporated as a detector as part of another technique, for example the use of an ultraviolet absorbance detector as part of a liquid chromatography system. In recent years there has been much enthusiasm for the research and development of hyphenated techniques, that is the interfacing/linking together of two or more techniques, because of the enhanced additional data that can be generated. [Pg.288]

Most real samples that are analysed are, unless they have been deliberately purified (and even then they may still be), actually made up from a number of different chemicals this is certainly trae for most colorants. As has already been discussed when considering molecular spectroscopy techniques, analysis of mixtures can lead to complex, incomplete or even unrcsolvable data. The answer/solution to problems of this type normally involves separation science, where there is selective or differential interaction/behaviour of the different components in the separation system. The principle separation sciences are chromatography and electrophoresis. [Pg.302]

In the face of this complexity there are few analytical techniques which do not apply1 An advanced iC process will utilize traditional bulk chemical analysis, i.e. chromatography, spectroscopy, titrimetry, etc., as well as the array of ion and electron beam techniques for thin film and small spot analysis. [Pg.14]

Second-order calibration depends critically on the underlying assumptions of linearity. One of the problems, e.g., in using a hyphenated technique such as chromatography-spectroscopy, is the poor reproducibility of the retention time axis. This destroys the trilinearity of the calibration model. For certain situations, this can be counteracted by using different types of three-way models (e.g. PARAFAC2 [Bro el al. 1999]), but in most of the cases extensive (manual) preprocessing is needed to linearize the data. This renders second-order calibration a less practical technique for such data. [Pg.284]

Composition - Each crude-oil field has a different composition, that can be established by a combination of gas-chromatography, fluorescence-spectroscopy, and infrared-spectroscopy techniques, and that may be used. [Pg.153]

FTIR Fourier transform infrared spectroscopy (technique useful in identifying and analyzing various unknown compounds, such as environmental pollutants) GC Gas chromatography (most commonly used analytical technique for organics) GC/MS Gas chromatography/mass spectrometry (technique based on chromatographic separation, followed by chemical or electron-impact ionization and identification of the mass spectra of the ionized fragments)... [Pg.8]

Spectroscopy is only one of the general methods of analysis used to monitor processes. Chromatography, electrochemical techniques and a broad range of physical measurements are commonly used [7] but are obviously beyond the scope of both this section and indeed this Handbook. The role of spectroscopy in process analysis has recently been reviewed [8]. [Pg.869]

R 663 D. Si and D. Zhong, Application of Liquid Chromatography-Spectroscopy Coupled Techniques to the Chemical Screening of Natural Products , Yaoxue Xuebao, 2002,37, 485... [Pg.48]

Quantification of microbial PHA using GC method is rapid, sensitive, reproducible, and requires only small amount of samples (5-10 mg) for the analysis. Other techniques of analysis such as IR spectrometry at 5.75 A (Juttner et al. 1975), two-dimensional fluorescence spectroscopy, flow cytometry (Degelau et al. 1995) HPLC (Karr et al. 1983), ionic chromatography, and enzymatic determination (Hesselmann et al. 1999) were also desalbed. For online determination of PHA content in recombinant E. coli system, Fourier transform mid-infrared spectrometry (FTIR) and microcalorimetric technique (Ruan et al. 2007 Jarute et al. 2004) were also reported. For precise composition determination and structural elucidation of PHA, a variety of nuclear magnetic resonance (NMR) spectroscopy techniques have also been applied and the most commonly used are proton ( H) and carbon-13 ( C) NMR (Doi et al. 1986 Jacob et al. 1986). [Pg.19]

Various types of modern food analytical techniques have been developed, including electrophoresis, chromatography, spectroscopy, rheological techniques, and sensory evaluation, to meet the challenge of providing information on the diverse components of these complex food materials. [Pg.1442]

See also Liquid Chromatography Overview Liquid Chromatography-Mass Spectrometry. Nuclear Magnetic Resonance Spectroscopy Overview Instrumentation. Nuclear Magnetic Resonance Spectroscopy Techniques Multidimensionai Proton. [Pg.2666]

See also Chromatography Overview. Liquid Chromatography Instrumentation Liquid Chromatography-Nuclear Magnetic Resonance Spectrometry. Nuciear Magnetic Resonance Spectroscopy Techniques Principles Multidimensional Proton Solid-State In Vivo Spectroscopy Using Localization Techniques. [Pg.3281]

See also Extraction Solid-Phase Extraction. Food and Nutritional Analysis Oils and Fats Fruits and Fruit Products. Lab-on-a-Chip Technologies. Liquid Chromatography Liquid Chromatography-Nuclear Magnetic Resonance Spectrometry. Nuclear Magnetic Resonance Spectroscopy Oven/iew Principles Instrumentation. Nuclear Magnetic Resonance Spectroscopy Applications Food. Nuclear Magnetic Resonance Spectroscopy Techniques Solid-State. Peptides. Radiochemical Methods Radiotracers Pharmaceutical Applications. [Pg.3287]

See also Capillary Electrophoresis Overview. Chir-optical Analysis. Liquid Chromatography Column Technology Mobile Phase Selection Reversed Phase Instrumentation Amino Acids. Mass Spectrometry Peptides and Proteins. Nuclear Magnetic Resonance Spectroscopy Techniques Nuclear Overhauser Effect. Proteins Traditional Methods of Sequence Determination Foods. [Pg.3564]

See alsa Gas Chromatography Overview. Infrared Spectroscopy Overview. Liquid Chromatography Size-Exclusion. Mass Spectrometry Overview. Nuclear Magnetic Resonance Spectroscopy Techniques ... [Pg.3826]

Modes of Adsorption of Sulfur-Containing Compounds. In typical gas oil, more than 70 different sulfur species can be detected by using gas chromatography-mass spectroscopy techniques. Moreover, the major components are alkylbenzothiophenes and alkyldibenzothiophenes. Consequently and to simplify studies already intrinsically complex, an impressive amovmt of studies were devoted to the HDS reactivity of the family of thiophene compovmds ((thiophene, BT, or DBT). The first step of any of these studies concerning the thiophene HDS mechanism is to describe the elemental steps of this process. The most general mechanism accepted in a solid-state point of view is to consider the HDS reaction as a four-electron reduction process releasing H2S and butadiene from thiophene (148). [Pg.1573]


See other pages where Chromatography spectroscopy, techniques is mentioned: [Pg.691]    [Pg.691]    [Pg.2]    [Pg.449]    [Pg.21]    [Pg.173]    [Pg.737]    [Pg.739]    [Pg.239]    [Pg.169]    [Pg.150]    [Pg.477]    [Pg.74]    [Pg.1222]    [Pg.253]    [Pg.155]    [Pg.436]    [Pg.304]    [Pg.89]    [Pg.678]    [Pg.3358]    [Pg.3359]    [Pg.566]    [Pg.969]   
See also in sourсe #XX -- [ Pg.43 ]




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