Scanning imaging system

Figure 4 Video micrograph (A) and Raman chemical image (B) of a monocrystalline silicon substrate with amorphous silicon deposited in a pattern on the substrate surface obtained using a commercial line-scan imaging system. 

Chao, K. et al. (2007) Hyperspectral-multispectral line-scan imaging system for automated poultry carcass inspection applications for food safety. Poult. Sci, 86 (11), 2450-2460. 

Chao, K., Yang, C.C., and Kim, M.S. (2010) Spectral line-scan imaging system for high-speed non-destructive wholesomeness inspection of broilers. Trends Food Sci. Technol, 21 (3), 129-137. 

Homogeneity of data. Homogeneous data will be uniform in structure and composition, usually possible to describe with a fixed number of parameters. Homogeneous data is encountered in simple NDT inspection, e.g. quality control in production. Inhomogeneous data will contain various combinations of indications from construction elements, defects and noise sources. An example of inhomogenous data are ultrasonic B-scan images as described in [Hopgood, 1993] or as encountered in the ultrasonic rail-inspection system described later in this paper. 

To evaluate the VIGRAL method, we scanned steel blocks with simulated flaws using a Flexilrak and a upi-50 instrument. This system allows for rapid and accurate acquisition of the desired data, including the A-scan, B-scan, and C-scan data, and serves to evaluate, offline, the V-scan image (Figure 8). 

The system should support all the inspection types available in the PSP-3 P-scan, T-scan and Through Transmission, TOFD and A-scan. It should be possible to record data for all the inspection types simultaneously. The developments in computer hardware, in particular disk storage, during the last years have made it feasable to increase the emphasis on the A-scan recording modes. It has also been feasible to extend the P-scan format to include P-scan image storage in a full 3D format, that allows cross-section views to be generated off-line. 

For ultrasonic imaging systems (B-, C- and C-scans) single-shot measurements, fast data recordings, and fast data transfer must be performed. 

The pulser/receiver HILL-SCAN 30XX boards satisfy DIN 25450. Typical applications are ultrasonie imaging systems for nuclear power stations and for aircraft, material characterization, transducer qualification, replacement of portable flaw detectors (inspections of welded joints), inspection of new materials, measurement systems with air eoupling. ... 

Cork T and Kino G S 1996 Confocal Scanning Optical Microscopy and Related Imaging Systems (New York Academic) Gu Min 1996 Principles of Three Dimensional Imaging In Confocal Microscopes (Singapore World Scientific)... 

Wokosin D L and White J G 1997 Optimization of the design of a multiple-photon excitation laser scanning fluorescence imaging system Proc. SPIE 2984 25-9... 

Unlike other infrared techniques, thermal or infrared imaging provides the means to scan the infrared emissions of complete machines, process or equipment in a very short time. Most of the imaging systems function much like a video camera. The user can view the thermal... 

FIGURE 10.13 The TLC profiles of labeled peaks isolated from [U- C]ascorbic-acid-modified calf lens protein obtained from Bio-Gel P-2 chromatography. Peaks 2 to 7 were spotted on a preparative silica gel TLC plate and developed with ethanol/ammonia (7 3, v/v). The fluorescence in each lane was detected by irradiation with a Wood s lamp at 360 nm, and the pattern of radioactivity was determined by scanning the plate with AMBIS imaging system. (Reprinted with permission from Cheng, R. et al., Biochim. Biophys. Acta, 1537, 14-26, 2001. Copyright (2001) Elsevier.)... 

Food typically is a complicated system with diverse interfaces. Stable air-water or oil-water interfaces are essential for the production of food foams and emulsions. Interface phenomena, therefore, attract great interest in the food industry. AFM provides enough resolution to visualize the interface structures, but it cannot be directly applied on air-liquid or liquid-liquid interfaces. Fortunately, the interface structure can be captured and transferred onto a freshly cleaved mica substrate using Langmuir-Blodgett techniques for AFM scan. Images are normally captured under butanol to reduce adhesion between the probe and the sample. Then, sample distortion or damage can be avoided (Morris et al, 1999). 

Figure 5.17 illustrates the principle of the STEM imaging system the probe remains parallel to the optic axis of the microscope as it scans. Two pairs of scan coils are used to pivot the beam about the front focal plane of the objective polepiece. 

Since TIRF produces an evanescent wave of typically 80 nm depth and several tens of microns width, detection of TIRF-induced fluorescence requires a camera-based (imaging) detector. Hence, implementing TIRF on scanning FLIM systems or multiphoton FLIM systems is generally not possible. To combine it with FLIM, a nanosecond-gated or high-frequency-modulated imaging detector is required in addition to a pulsed or modulated laser source. In this chapter, the implementation with of TIRF into a frequency-domain wide-field FLIM system is described. 

Separate products by agarose gel electrophoresis Slain with cl Iridium bromide and scan with suitable imaging system c.g. Kodak EDAS 2 0... 

Fig. 3. Comparisons of wide-field (A) and confocal fluorescence images (B, mesoglea level C, apical) of rhodamine phalloidin-stained F-actin in a whole-mount hydra tentacle. The hydra was fixed and stained as described in Chapter 18. The bar represents 25 pm. All images were collected with a Nikon (New York) Microphot FX microscope (x40 objective lens). Confocal images were collected with the microscope connected to a Bio-Rad (Hercules, CA) MRC600 laser-scanning confocal system.

Fig. 5. Optical sectioning of rhodamine phalloidin-stained F-actin in a neutrophil migrating through a 5-pm pore of a polycarbonate membrane. The neutrophil migration is stimulated in response to 10 M Af-formytmethionyl-leucy 1-phenylalanine. (A), (B), and (C) correspond to O.S-pm optical sections indicated as sections A, B, and C, respectively, in Fig. 4. The bar represents 10 pm. The images were collected with a Nikon Microphot FX microscope (x60 Plan-apochromat lens, numerical aperture, 1.6) connected to a Bio-Rad MRC600 laser-scanning confocal system.

Figure l6 Scanned image of an entire trailer truck. This B/W image is typically presented as a false color image to enhance attenuation information about the contents. The imaging system is optimized to accommodate the characteristics of human visual response. 

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