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Sample manipulation

The 3D positions of internal defects are calculated with a stereoscopic approach supporting arbitrary sample manipulations using an arbitrary number of views. The volumes of the defects are calculated using intensity evaluation. [Pg.488]

The setup as seen in Figure 1 mainly consists of a Varian Linatron 3000A linear accelerator (LINAC) as radiation source, a rotational stage for sample manipulation, and a two-dimensional high-energy x-ray detector array consisting of four amorphous silicon area detectors Heimann RIS 256. The source to detector distance is 3.7 m. [Pg.492]

The X-ray instrumentation requires a commercial small angle X-ray camera, a standard fine structure X-ray generator and a sample manipulator if scanning is requested. The essential signal is the relative difference between the refraction level Ir and the absorption level Ia. Both levels are measured simultaneously by two scintillation detectors. At fixed angles of deflection this signal depends solely on the inner surface density factor C and thickness d of the sample [2] ... [Pg.558]

A fully automated microscale indentor known as the Nano Indentor is available from Nano Instmments (257—259). Used with the Berkovich diamond indentor, this system has load and displacement resolutions of 0.3 N and 0.16 nm, respectively. Multiple indentations can be made on one specimen with spatial accuracy of better than 200 nm using a computer controlled sample manipulation table. This allows spatial mapping of mechanical properties. Hardness and elastic modulus are typically measured (259,260) but time-dependent phenomena such as creep and adhesive strength can also be monitored. [Pg.195]

A typical LIMS instrument accepts specimens up to 19 mm (0.75 in) in diameter and up to 6 mm in thickness. Custom designed instruments exist, with sample manipulation systems that accept much larger samples, up to a 6-in wafer. Although a flat sample is preferable and is easier to observe with the instrument s optical system, irregular samples are often analyzed. This is possible because ions are produced and extracted from pm-sized regions of the sample, without much influence from nearby topography. However, excessive sample relief is likely to result in reduced ion signal intensity. [Pg.596]

A versatile Laser-SNMS instrument consists of a versatile microfocus ion gun, a sputtering ion gun, a liquid metal ion gun, a pulsed flood electron gun, a resonant laser system consisting of a pulsed Nd YAG laser pumping two dye lasers, a non-resonant laser system consisting of a high-power excimer or Nd YAG laser, a computer-controlled high-resolution sample manipulator on which samples can be cooled or heated, a video and electron imaging system, a vacuum lock for sample introduction, and a TOF mass spectrometer. [Pg.135]

Harris, W. E., Sampling, Manipulative, Observational, and Evaluative Errors, International Laboratory, Jan-Feb 1978, 53-62. [Pg.404]

By incorporating the entire analytical scheme (enzyme reaction and electrochemical detection) into the flow system a great improvement in precision can be realized. Sample manipulation is minimized because only a single injection into the flow system is required versus sampling of aliquots for the off-line method. Precision is also improved because the timing of the enzyme reaction and detection are much better controlled in the flow system. Finally, less of both enzyme and sample are needed with on-line enzyme reactor methods. [Pg.29]

Following RM certificate instructions for material usage and handling, incorporate the RM into the scheme of analysis at the earliest stage possible, i.e. prior to the beginning of sample decomposition. Take it through the entire analytical procedure at the same time and under the identical conditions as the actual analytical samples in order to correctly monitor all the sample manipulation and measurement steps. [Pg.217]

In the last several years, on-line extraction systems have become a popular way to deal with the analysis of large numbers of water samples. Vacuum manifolds and computerized SPE stations were all considered to be off-line systems, i.e., the tubes had to be placed in the system rack and the sample eluate collected in a test-tube or other appropriate vessel. Then, the eluted sample had to be collected and the extract concentrated and eventually transferred to an autosampler vial for instrumental analyses. Robotics systems were designed to aid in these steps of sample preparation, but some manual sample manipulation was still required. Operation and programming of the robotic system could be cumbersome and time consuming when changing methods. [Pg.824]

Mixing, wrist shaking, or tumbling combinations offer a simple, effective, but time-consuming and not highly reproducible method of extraction. Sample-to-solvent ratios are similar to Soxhlet ratios. Although sample manipulation is reduced, this technique requires nearly as much time as the Soxhlet method. Shake-flask extraction is low cost. [Pg.66]

Figure 6. Plan of the target preparation facilities consisting of UHV preparation chamber (a), (reactive) ion etching chamber (b), ion etching gun (c), laser (d), photon detector (e), transfer arms (f), Auger system for surface analysis (g), sample manipulator and annealing facility (h), load lock and optical microscope for viewing sample (i), evaporator (j), transmission diffractometer (k), and vacuum tank for main spectrometer (1). Figure 6. Plan of the target preparation facilities consisting of UHV preparation chamber (a), (reactive) ion etching chamber (b), ion etching gun (c), laser (d), photon detector (e), transfer arms (f), Auger system for surface analysis (g), sample manipulator and annealing facility (h), load lock and optical microscope for viewing sample (i), evaporator (j), transmission diffractometer (k), and vacuum tank for main spectrometer (1).
The present chapter does not consider analysis of extracted protein biomarkers but rather focuses on strategies for rapid chemotaxonomic analysis of intact microorganisms with automated sample manipulation. Rapid means less than 5 minutes. Advantages of the application of bioinformatics and proteomics strategies for rapid identification of microorganisms include the following ... [Pg.260]

Due to scientific and public concern about environmental pollution, new developments in environmental analysis are focused on the implementation of environmental-friendly practices in the laboratories. Main strategies are addressed to saving energy and to reduce solvent consumption with the minimum sample manipulation by using on-site, online, and direct analysis (e.g., biosensors) [42],... [Pg.36]

Use of immobilised chelating agents for sequestering trace metals from aqueous and saline media presents several significant advantages over chelation-solvent extraction approaches to this problem [193,194], With little sample manipulation, large preconcentration factors can generally be realised in relatively short times with low analytical blanks. [Pg.160]


See other pages where Sample manipulation is mentioned: [Pg.489]    [Pg.1017]    [Pg.939]    [Pg.1824]    [Pg.109]    [Pg.507]    [Pg.568]    [Pg.267]    [Pg.194]    [Pg.21]    [Pg.159]    [Pg.99]    [Pg.328]    [Pg.211]    [Pg.468]    [Pg.422]    [Pg.921]    [Pg.44]    [Pg.127]    [Pg.191]    [Pg.31]    [Pg.189]    [Pg.275]    [Pg.281]    [Pg.284]    [Pg.276]    [Pg.78]    [Pg.79]    [Pg.98]    [Pg.101]    [Pg.126]    [Pg.546]    [Pg.240]    [Pg.157]    [Pg.335]    [Pg.46]   
See also in sourсe #XX -- [ Pg.323 ]




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Microfluidic Sample Manipulation

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