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Laboratories, chip

Shoebox-sized lab-on-a-chip laboratories personal dmg manufacture general advantages of micro flow Merck s production nitrations HTS parallel catalyst testing turnkey bench-scale test station standardization cube-like modules [210],... [Pg.86]

Microchip laboratories have many advantages. They require only tiny amounts of sample. This is especially advantageous for expensive, difficult-to-prepare materials or in cases such as criminal investigations, where only small amounts of evidence may exist. The chip laboratories also minimize contamination because they represent a closed system once the material has been introduced to the chip. The chips also can be made to be disposable to prevent cross-contamination of different samples. [Pg.98]

The chip laboratories also present some difficulties not found in macroscopic laboratories. The main problem concerns the large surface area of the capillaries and reaction chambers relative to the sample volume. Molecules or biological cells in the sample solution encounter so much wall that they may undergo unwanted reactions with the wall materials. Glass seems to present the least of these problems, and the walls of silicon chip laboratories can be protected by formation of relatively inert silicon dioxide. Because plastic is inexpensive, it seems a good choice for disposable chips, but plastic also is the most reactive with the samples and the least durable of the available materials. [Pg.98]

Laboratorial microsystem Micro-total analysis system (pTAS) MTAS On-chip laboratory... [Pg.1511]

Mix 6 2 ml. (6 4 g.) of pure ethyl acetoacetate and 5 ml. of pure phenylhydrazine in an evaporating-basin of about 75 ml. capacity, add 0 5 ml. of acetic acid and then heat the mixture on a briskly boiling water-bath (preferably in a fume-cupboard) for I hour, occasionally stirring the mixture with a short glass rod. Then allow the heavy yellow syrup to cool somewhat, add 30-40 ml. of ether, and stir the mixture vigorously the syrup may now dissolve and the solution shortly afterwards deposit the crystalline pyrazolone, or at lower temperatures the syrup may solidify directly. Note. If the laboratory has been inoculated by previous preparations, the syrup may solidify whilst still on the water-bath in this case the solid product when cold must be chipped out of the basin, and ground in a mortar with the ether.) Now filter the product at the pump, and wash the solid material thoroughly with ether. Recrystallise the product from a small quantity of a mixture of equal volumes of water and ethanol. The methyl-phenyl-pyrazolone is obtained... [Pg.271]

Also, pilot plant and laboratory scale anaerobic studies have demonstrated successful treatment of wastewaters of 5,000 to 50,000 mg/L GOD from corn chips containing soluble and colloidal corn starch and protein, cheese whey, organic chemicals, food, bakeiy, breweiy, paper mill foul condensate, paint, and numerous other hazardous anci non-hazardous materials. [Pg.2226]

Figure 7.3. The evolution of electronics a vacuum tube, a discrete transistor in its protective package, and a 150 nun (diameter) silicon wafer patterned w ith hundreds of integrated circuit chips. Each chip, about I enr in area, contains over one million transistors, 0..35 pm in size (courtesy M.L. Green, Bell Laboratories/Lucent Technologies). Figure 7.3. The evolution of electronics a vacuum tube, a discrete transistor in its protective package, and a 150 nun (diameter) silicon wafer patterned w ith hundreds of integrated circuit chips. Each chip, about I enr in area, contains over one million transistors, 0..35 pm in size (courtesy M.L. Green, Bell Laboratories/Lucent Technologies).
The chloride is mixed on a laboratory scale with xs Ca (powder or chips) in an Fe tube in a high-T glass distillation vessel. The Fe tube protects the glass from corrosive attack by the alkali-metal vapors. The vessel is inclined and evacuated while slowly heating to 700-800°C. The liberated Rb or Cs distills onto the cooler upper walls of the vessel and runs into integral glass ampules, which are sealed under vacuum for storage. Further purification is achieved by repeated. vacuum distillation at 300°C. Yields arc theoretical. [Pg.348]

Sensors of the future will be incredibly small and capable. Many will feature a chemical laboratory and a computer on a chip. They will enable chemical engineers to detect chemical compositions inside hostile process enviromnents and revolutionize their ability to control processes. [Pg.18]

FIGURE 4.1 Chemical reactions are used to achieve the fine structures seen in modern integrated circuits. This electron micrograph shows a transistor in a "cell" of a 1-mega-bit dynamic random access memory chip. The distance between features is about 1 pm. Courtesy, AT T Bell Laboratories. [Pg.53]

Colors in a laboratory should be coordinated, just as in a home. If pre-finished work benches are to be installed, they might set the color scheme. While they are available in several colors or combination of colors, the choice is not unlimited. In one case, the laboratory operator was color blind, so his wife took over the job as decorator. First, she selected a two-color scheme for the work benches. Color chips in hand, she then chose a floor covering from a number of samples submitted. For the wall paint, she found a standard color of the recommended quality that harmonized with the cabinets. A few appropriate charts and a colorful cloth wall-hanging of pipes and valves completed the decor. The result received many favorable comments from visitors to the facility. [Pg.71]

The current trend in analytical chemistry applied to evaluate food quality and safety leans toward user-friendly miniaturized instruments and laboratory-on-a-chip applications. The techniques applied to direct screening of colorants in a food matrix include chemical microscopy, a spatial representation of chemical information from complex aggregates inside tissue matrices, biosensor-based screening, and molec-ularly imprinted polymer-based methods that serve as chemical alternatives to the use of immunosensors. [Pg.523]

The project is managed through the Laboratory of the Government Chemist in Teddington, UK, and is part of the British government s Foresight link program [45]. The cost of the Lab-on-a-Chip project was 3.2 million. Two key tasks are the exploration of reactions and processes on a micro-scale and the commercialization of the results. [Pg.21]

As a second example, several Hantzsch syntheses using diverse ring-substituted 2-bromoacetophenones and 1-substituted-2-thioureas are given. For these reactions, comparative and better yields were achieved when using a micro-mixing tee chip reactor as compared with conventional laboratory batch technology. The increase in yield amounted to about 10-20% [156, 157]. [Pg.69]

Mikroreaktorenfur die chemische Synthese, Nachrichten aus der Chemie, May 2000 Chip technology initiates quest for small structures better temperature control on the small scale fast mixing by diffusion several kg productivity per day no novel, but better chemistry perfect control over process parameters corresponding increase in selectivity basic micro-reactor functions selected examples of use micro reactors as routine tools in the laboratory first start-up companies [113],... [Pg.87]

Das Chemidabor im Mikrochip, Blick durch die Wirtschafi, December 1997 Chemtel glass chip of Orchid Biocomputer, Princeton 144 cells for parallel processing matchbox-sized system with many devices micro pumps with no movable parts 10 nl internal volume carrying out of different reactions in parallel fashion complete chemistry laboratory en miniature 10 000 cells as future-development task [223],... [Pg.89]

Lindner, D., The pChem Lab project micro total analysis system R D at Sandia National Laboratories, Lab Chip 1 (2001) 15N-19N. [Pg.111]

Liquid transport is achieved by hydrostatic action, pumping or electroosmotic flow (EOF). So far, chip reactors have been employed at low to very low flow rates, e.g. from 1 ml min to 1 pi min. Applications consequently were restricted to the laboratory-scale or even solely to analytics. However, this is not intrinsic. By choosing larger internal dimensions, similar throughputs as for the other classes of liquid or liquid/liquid micro reactors are in principle achievable. [Pg.382]


See other pages where Laboratories, chip is mentioned: [Pg.54]    [Pg.231]    [Pg.854]    [Pg.54]    [Pg.231]    [Pg.854]    [Pg.277]    [Pg.149]    [Pg.146]    [Pg.173]    [Pg.396]    [Pg.262]    [Pg.908]    [Pg.195]    [Pg.54]    [Pg.1358]    [Pg.21]    [Pg.88]    [Pg.108]    [Pg.682]    [Pg.706]    [Pg.277]    [Pg.67]    [Pg.748]   
See also in sourсe #XX -- [ Pg.152 ]

See also in sourсe #XX -- [ Pg.138 ]




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Chip-based laboratories

Laboratory on a chip

Laboratory-on-a-chip systems

Microfluidic laboratory chips

Silicon chip laboratories

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