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Applications line identification

Applications Rather intractable samples, such as organic polymers, are well suited to FD, which avoids the need for volatilisation of the sample. Since molecular ions are normally the only prominent ions formed in the FD mode of analysis, FD-MS can be a very powerful tool for the characterisation of polymer chemical mixtures. Application areas in which FD-MS has played a role in the characterisation of polymer chemicals in industry include chemical identification (molecular weight and structure determination) direct detection of components in mixtures off-line identification of LC effluents characterisation of polymer blooms and extracts and identification of polymer chemical degradation products. For many of these applications, the samples to be analysed are very complex... [Pg.375]

However, the main reason for the lack of wide application of on-line adaptive control is the lack of economic incentive. On-line identification is rarely required because it is usually possible to predict with off-line tests how the controller must be retuned as conditions vary. The dynamics of the process are determined at different operating conditions, and appropriate controller settings are determined for all the different conditions. Then, when the process moves from one operating region to another, the controller settings are automatically changed. This is called openloop-adaptive control or atn scheduling. [Pg.263]

The method of lines and system identification are not restricted in their applicability. System identification is preferred because the order of the resulting state space model is significantly lower. Another advantage of system Identification is that it can directly be applied on experimental data without complicated analysis to determine the kinetic parameters. Furthermore, no model assumptions are required with respect to the form of the kinetic expressions, attrition, agglomeration, the occurence of growth rate dispersion, etc. [Pg.157]

Stephanopoulos, G. Application of macroscopic balances and bioenergetics of growth to the on-line identification of biological reactors. Ann. N. Y. Acad. Sci. 1986, 469 (Biochem. Eng. 4), 332-349. [Pg.949]

TOF (time-of-fiight) mass spectrometers are also increasing in popularity and have been successfully coupled with gas chromatographs. In fact, the first successful on-line identification of GG eflBiuents by MS was with a TOF (29). TOF spectrometers are sensitive instruments. They are by far the fastest scanning of the three major spectrometer types— 50,000 lines per second. This feature makes it the only mass analyzer available for fast reaction research. The TOF also has a stable mass scale and can be computerized readily. However, resolution and mass range of the TOF instrument are low—about 500 amu. This may limit its application for pesticide residue analysis however, mass spectra of organophos-... [Pg.44]

Applied Spectroscopy 51, No.6, June 1997, p.856-65 APPLICATION OF A SPECTROSCOPIC INFRARED FOCAL PLANE ARRAY(FPA) SENSOR FOR ON-LINE IDENTIFICATION OF PLASTIC WASTE... [Pg.85]

Spectroscopic techniques have been employed extensively for monitoring and control of processes in different fields. Since a detailed review of the applications of spectroscopic techniques in distinct areas is certainly beyond the objectives of the chapter, the interested reader should refer to textbooks and surveys for additional details [ 10,27,30,33,43,44]. It is also important to emphasize that most publications available in the field of polymer and polymerization reactions make use of spectrometers for off-line characterization of polymer properties. Typical applications include identification of polymer materials [82], evaluation of copolymer and polymer blend compositions [83, 84], evaluation of monomer and polymer compositions during polymerizations [85], determination of additive content in polymer samples [86, 87], and estimation of end-use properties of polymer materials. End-use properties analyzed include the degree of crystallinity of polymer samples [88], the degree of orientation of polymer films [85], the hydroxyl number of polyols [89], the melt flow index of polymer pellets [90], and the intrinsic viscosity of polymer powders [91], the morphology of... [Pg.118]

A third model-based approach is neural predictive control, which is a neural network version of nonlinear model predictive control [Trajanoski and Wach, 1998]. In this approach, the neural network is used for off-line identification of a system model, which is then used to design a nonlinear model predictive controller. This design may provide suitable control of nonhnear systems with time-delays and thus maybe particularly useful in biomedical applications. Recent computer simulation studies have demonstrated positive results for control of insulin delivery [Trajanoski and Wach, 1998],... [Pg.223]

Tzes, A. P., Yurkovich, S., "Application and comparison of on-line identification methods for flexible manipulator control". The International Journal of Robotics Research, Vol. 10, N° 5, October 1991, pp 515-527. [Pg.164]

Enter in the spaces provided, the name and address of each location (other than POTWs) to which you ship or transfer wastes containing toxic chemicals. Do not include locations to which you ship the toxic chemical for recycle or reuse, tf you do not ship ortransfer wastes containing toxic chemicals to offsite locations, enter not applicable, NA in the off-site location name line of 2.1. Also enter the EPA Identification Number (RCRA I.D. Number) for each such location if known to you. This number may be found on the Uniform Hazardous Waste Manifest, which is required by RCRA regulations. Also indicate in the space provided whether the location is owned or controlled by yourfacility or your parent company. If thefacility does not have a RCRA 1.0. number, enter not applicable, NA, in this space. [Pg.36]

Figure 10.13 GC clrromatogram obtained after on-line LC-GC(ECD) of a human milk sample analysed for PCBs (attenuation X 64). Peak identification is as follows (1) PCB 28 (2) PCB 118 (3) PCB 153 (4) PCB 138 (5) PCB 180 (6) PCB 170 (7) PCB 207. Reprinted from Journal of High Resolution Chromatography, 20, G. R. van der Hoff et al, Determination of organochlorine compounds in fatty matiices application of normal-phase LC clean-up coupled on-line to GC/ECD , pp. 222-226, 1997, with permission from Wiley-VCH. Figure 10.13 GC clrromatogram obtained after on-line LC-GC(ECD) of a human milk sample analysed for PCBs (attenuation X 64). Peak identification is as follows (1) PCB 28 (2) PCB 118 (3) PCB 153 (4) PCB 138 (5) PCB 180 (6) PCB 170 (7) PCB 207. Reprinted from Journal of High Resolution Chromatography, 20, G. R. van der Hoff et al, Determination of organochlorine compounds in fatty matiices application of normal-phase LC clean-up coupled on-line to GC/ECD , pp. 222-226, 1997, with permission from Wiley-VCH.
Electropherograms of a urine sample (8 ml) spiked with non-steroidal anti-inflammatory drugs (10 p-g/ml each) after direct CE analysis (b) and at-line SPE-CE (c). Peak identification is as follows I, ibuprofen N, naproxen K, ketoprofen P, flurbiprofen. Reprinted from Journal of Chromatography, 6 719, J. R. Veraait et al., At-line solid-phase exti action for capillary electrophoresis application to negatively charged solutes, pp. 199-208, copyright 1998, with permission from Elsevier Science. [Pg.287]

It is of interest to examine the development of the analytical toolbox for rubber deformulation over the last two decades and the role of emerging technologies (Table 2.9). Bayer technology (1981) for the qualitative and quantitative analysis of rubbers and elastomers consisted of a multitechnique approach comprising extraction (Soxhlet, DIN 53 553), wet chemistry (colour reactions, photometry), electrochemistry (polarography, conductometry), various forms of chromatography (PC, GC, off-line PyGC, TLC), spectroscopy (UV, IR, off-line PylR), and microscopy (OM, SEM, TEM, fluorescence) [10]. Reported applications concerned the identification of plasticisers, fatty acids, stabilisers, antioxidants, vulcanisation accelerators, free/total/bound sulfur, minerals and CB. Monsanto (1983) used direct-probe MS for in situ quantitative analysis of additives and rubber and made use of 31P NMR [69]. [Pg.36]

Applications On-line SPE-GC and SPE-GC-MS couplings find wide application for sample cleanup of biological, environmental and industrial analysis of aqueous samples [67]. SPE-GC-AED/MS is ideally suited for the (nontarget) screening of hetero-atom-containing compounds in aqueous samples, and allows confirmation plus identification in one run [68]. Specific applications of hyphenated SPE-GC systems for polymer/additive analysis were not identified. [Pg.437]

Applications With the current use of soft ionisation techniques in LC-MS, i.e. ESI and APCI, the application of MS/MS is almost obligatory for confirmatory purposes. However, an alternative mass-spectrometric strategy may be based on the use of oaToF-MS, which enables accurate mass determination at 5 ppm. This allows calculation of the elemental composition of an unknown analyte. In combination with retention time data, UV spectra and the isotope pattern in the mass spectrum, this should permit straightforward identification of unknown analytes. Hogenboom et al. [132] used such an approach for identification and confirmation of analytes by means of on-line SPE-LC-ESI-oaToFMS. Off-line SPE-LC-APCI-MS has been used to determine fluorescence whitening agents (FWAs) in surface waters of a Catalan industrialised area [138]. Similarly, Alonso et al. [139] used off-line SPE-LC-DAD-ISP-MS for the analysis of industrial textile waters. SPE functions here mainly as a preconcentration device. [Pg.448]

In chromatography-FTIR applications, in most instances, IR spectroscopy alone cannot provide unequivocal mixture-component identification. For this reason, chromatography-FTIR results are often combined with retention indices or mass-spectral analysis to improve structure assignments. In GC-FTIR instrumentation the capillary column terminates directly at the light-pipe entrance, and the flow is returned to the GC oven to allow in-line detection by FID or MS. Recently, a multihyphenated system consisting of a GC, combined with a cryostatic interfaced FT1R spectrometer and FID detector, and a mass spectrometer, has been described [197]. Obviously, GC-FTIR-MS is a versatile complex mixture analysis technique that can provide unequivocal and unambiguous compound identification [198,199]. Actually, on-line GC-IR, with... [Pg.458]

MSD provides molecular weight, fragmentation information and mass selectivity. Also, simultaneous GC-MS/MIP-AES has been described, using both a low-pressure and an atmospheric-pressure splitter [336]. The combination of MS and AED data sets provides the potential for application to a wide range of analytical problems, such as screening for the presence of hetero-atom-containing analytes (AED), identification and confirmation (MS) and quantification (MS, AED). On-line LVI-GC-AED/MS (dual detection) has been described with small (i.e. less than 0.5 s) differences in retention time of a compound with AED and MS detection [67], The dual-hyphenation set-up largely eliminates data-interpretation problems caused by small differences in retention time, or retention indices and is,... [Pg.473]


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See also in sourсe #XX -- [ Pg.149 , Pg.150 , Pg.151 , Pg.152 , Pg.153 , Pg.154 , Pg.155 , Pg.156 ]




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