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Chip design

The design of the Pd-membrane reactor was based on the chip design of reactor [R 10]. The membrane is a composite of three layers, silicon nitride, silicon oxide and palladium. The first two layers are perforated and function as structural support for the latter. They serve also for electrical insulation of the Pd film from the integrated temperature-sensing and heater element. The latter is needed to set the temperature as one parameter that determines the hydrogen flow. [Pg.288]

The use of electrically-gated solute injection into the electrophoresis system simplifies the chip design as electrical connections are easy to implement as compared to the microfluidics part of the chip. Voltage waveform manipulation via hardware and software are relatively easy to control and implement. [Pg.106]

Banerjee, K. Souri, S. J. Kapur, P. Saraswat, K. C. 2001. 3-D ICs A novel chip design for improving deep-submicrometer interconnect performance and systems-on-chip integration. Proc. IEEE 89 602-633. [Pg.443]

Bergkvist, J., Ekstrom, S., Wallman, L., Lofgren, M., Marko-Varga, G., Nilsson, J., and Laurell, T. (2002). Improved chip design for integrated solid-phase microextraction in on-line proteomic sample preparation. Proteomics 2, 422—429. [Pg.517]

Fig. 5.9 Design of the chip-based enzyme ESI-MS assay. MS instrument Ion-trap mass spectrometer (LCQ Deca, Thermo Electron). I Sample components/inhibitors injected by flow injection or eluting from capillary HPLC column. E Infusion pump delivering the enzyme cathepsin B. S infusion pump delivering the substrate Z-FR-AMC. Micro-chip design Vrije Universiteit Amsterdam. Micro-chip production Micronit Microfluidics BV (Enschede, The Netherlands). Fig. 5.9 Design of the chip-based enzyme ESI-MS assay. MS instrument Ion-trap mass spectrometer (LCQ Deca, Thermo Electron). I Sample components/inhibitors injected by flow injection or eluting from capillary HPLC column. E Infusion pump delivering the enzyme cathepsin B. S infusion pump delivering the substrate Z-FR-AMC. Micro-chip design Vrije Universiteit Amsterdam. Micro-chip production Micronit Microfluidics BV (Enschede, The Netherlands).
Figures 6.9 and 6.14 show details of the chip design. Base fingers are connected, by the first level of metal, to the pad in the center of the chip by the cross-shaped bus and are further connected to another bus, which runs all around the chip. The emitter fingers are connected by the second-level metal all over the active area, excluding the center pad for the base. Figures 6.9 and 6.14 show details of the chip design. Base fingers are connected, by the first level of metal, to the pad in the center of the chip by the cross-shaped bus and are further connected to another bus, which runs all around the chip. The emitter fingers are connected by the second-level metal all over the active area, excluding the center pad for the base.
Reliability and Degradation of lll-V Optical Devices, Osamu Ueda System-on-a-Chip Design and Test, Rochit Rajsuman... [Pg.213]

Figure 2.6 Different types of recesses fabricated in the channel wall of the chip designed for trapping organic droplets [66]. Figure 2.6 Different types of recesses fabricated in the channel wall of the chip designed for trapping organic droplets [66].
This trend conforms to a pattern foreseen in 1965 by Gordon Moore (1929- ), cofounder of the Intel Corporation. Moore predicted that the number of circuits on a silicon chip would double every year, a projection he later changed to a doubling every 18 to 24 months. Progress in chip design has followed Moore s Law with remarkable accuracy ever since. If that law continues to hold true, one can expect processors with a billion transistors per chip sometime before the year 2015. [Pg.93]

Semiconductor (transistor) biosensors are widely used. They possess a several process advantages over the others small size, good reproducibility and high sensitivity, multipurpose chip design, accessibility and low price. [Pg.291]

In order to reduce variations in flow due to secondary forces such as capillary forces within reservoirs, the flow resistance at each port is increased by using a long serpentine path as a flow restrictor (see Figure 2.37). This chip design also contains the so-called pair-well design so that two channels from the pair wells (e.g., wells 1 and 8) are connected to a common node. Since the pair channels have the same flow resistance, the change of flow in one channel could be easily compensated by that from another channel and so keeping the main channel flow constant. For instance, a 40% flow in the main channel can be achieved by either -4% from well 1 and +44% from well 8, or 4% from well 1 and 36% from well 8 [295],... [Pg.52]

FIGURE 2.37 Chip design optimized for experiments using hydrodynamic flow control. The chip has the pair-well design suitable for dilution and enzymatic studies [295]. Reprinted with permission from Springer-Verlag. [Pg.52]

FIGURE 7.27 Micromachined ISE chip, (a) Schematic drawing of a sensor chip design with channels and reservoirs point A, inlet for U-channel point B, outlet for U-channel point C, inlet for sample channel point D, junction structure, where membrane contacts sample solution and point E, outlet for sample channel. The diagram illustrates the complete filling of the silanized U-channel with an organic membrane cocktail, (b) Scaled diagram of the 12- x 6-mm chip [766]. Reprinted with permission from the American Chemical Society. [Pg.222]

Chip Design Flow MS Mode Analytes Single-Channel ESI Chip Sample Treatment Separation Ref. [Pg.240]

Research on the integration of PCR and DNA analysis has been very active. For comparison, the PCR chip designs and PCR mixtures are tabulated in Tables 9.1 and 9.2, respectively. [Pg.296]

FIGURE 10.12 Chip design for protein separation. The wells are shown in light gray. Well D4 is the SDS dilution well and is connected to both sides of the dilution intersection. Wells A4 and C4 are the separation buffer and waste wells, and B4 and D3 are used as load wells. All other wells contain samples [1034]. Reprinted with permission from the American Chemical Society. [Pg.351]

Figure 21 Schematic of aqueous electrode chip design (Jenkins et at, 2005 reproduced by permission of the Royal Society of Chemistry). Figure 21 Schematic of aqueous electrode chip design (Jenkins et at, 2005 reproduced by permission of the Royal Society of Chemistry).
In mathematical system theory, the subject of model reduction has been studied for about 30 years. The focus is on model reduction of linear systems, in particular methods based on singular value decomposition. One of the best known of these methods is balanced truncation. It is used extensively for various engineering purposes, such as electronic chip design and the reduction of models of aerospace structures. This method does not require the type of a priori information about the system mentioned above. Only recently has it been tried out on biochemical systems [105, 106]. [Pg.410]

Smith Douglas, HDL Chip Design, Doone Publications, AL, 1996, ISBN 0-9651934-3-8. [Pg.210]

In 2004, the FDA approved a microarray chip designed to routinely identify polymorphisms of drug-metabolizing enzymes related to cytochrome P450 drug metabolism. [Pg.859]

Figures 2 and 3 show that the DRAM chip perforMance has been iMproved even though the chip functionality has increased for the accelerated tests used by the seMiconductor industry. The 85 C/85X RH results are better because of a coMbination of iMproveMents in the chip design, the Manufacturing procedures and the epoxy encapsu-lent. The teMperature cycle test results, however, were priMarily improved by converting to a "low stress" epoxy encapsulant. The im-proveMent in the pressure cooker and the 125 C operating life (Figure 3) was also due to a coMbination of iMproveMents, including those in the epoxy encapsulant. These iMproveMents in device reliability are especially reMarkable when it is realized that the chip susceptibility to contaminants and stress has increased tremendously due to the 60-fold increase to functionality. Figures 2 and 3 show that the DRAM chip perforMance has been iMproved even though the chip functionality has increased for the accelerated tests used by the seMiconductor industry. The 85 C/85X RH results are better because of a coMbination of iMproveMents in the chip design, the Manufacturing procedures and the epoxy encapsu-lent. The teMperature cycle test results, however, were priMarily improved by converting to a "low stress" epoxy encapsulant. The im-proveMent in the pressure cooker and the 125 C operating life (Figure 3) was also due to a coMbination of iMproveMents, including those in the epoxy encapsulant. These iMproveMents in device reliability are especially reMarkable when it is realized that the chip susceptibility to contaminants and stress has increased tremendously due to the 60-fold increase to functionality.

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See also in sourсe #XX -- [ Pg.46 ]




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