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Sequence developing chamber

FIGURE 6.3 Sequence developing chamber by Buncak 1 — support with mobile phase source (reservoir), 2 — holding frame, 3 — magnet holder, 4 — magnet, 5 — cover plate, 6 — TLC plate, 7 — wick with iron core, 8 — solvent entry. (From Buncak, P., GIT Fachz. Lab. (Suppl., Chromatographie), G-I-T-Verlag, Darmstadt, 3-8, 1982. With permission.)... [Pg.134]

The Aromax process was developed in the early 1970s by Toray Industries, Inc. in Japan (95—98). The adsorption column consists of a horizontal series of independent chambers containing fixed beds of adsorbent. Instead of a rotary valve, a sequence of specially designed on—off valves under computer control is used to move inlet and withdrawal ports around the bed. Adsorption is carried out in the Hquid phase at 140°C, 785—980 kPA, and 5—13 L/h. PX yields per pass is reported to exceed 90% with a typical purity of 99.5%. The first Aromax unit was installed at Toray s Kawasaki plant in March 1973. In 1994, IFP introduced the Eluxyl adsorption process (59,99). The proprietary adsorbent used is designated SPX 3000. Individual on-off valves controlled by a microprocessor are used. Raman spectroscopy to used to measure concentration profiles in the column. A 10,000 t/yr demonstration plant was started and successfully operated at Chevron s Pascagoula plant from 1995—96. IFP has Hcensed two hybrid units. [Pg.420]

As the density of information derived from efforts to sequence, map and identify human genes increased, so did the demand for analytical tools capable of exploiting this information. DNA microarrays were developed in response to this demand. Southern(69) was the first to describe parallel, in situ ohgonucleotide synthesis as a means of generating oligonucleotide probe arrays on solid supports for highly parallel hybridization analysis. Southern s method uses standard nucleotide synthetic reactions to synthesize the oligonucleotides. The reactions are carried out in a movable chamber, which provides a physical barrier between the reaction chamber and the intended synthesis area. [Pg.12]

The Bone Chamber sediments have mass susceptibilities of 500-1000 x 10 m kg, greater than those for pristine aeolian sediments such as the Chinese loesses, which typically have mass susceptibilities of the order of 10-100 x 10" m kg (e.g., Heller and Liu, 1984 Chen et al., 1999). Palaeosols developed within loess sequences, however. [Pg.63]

Some of the physical and chemical constraints on the flame atomization process — which usually precluded application to solid samples — were overcome with the advent of flameless atomization, initially accomplished with the pyrolytic coated graphite tube (or carbon rod-type) furnace atomizer. The graphite tube is a confined furnace chamber where pulsed vaporization and subsequent atomization of the sample is achieved by raising the temperature with a programmed sequence of electrical power. A dense population of ground state atoms is produced as a result for an extended interval in relation to the low atom density and short residence time of the flame. The earliest use of furnace devices in analytical atomic spectroscopy is credited to a simultaneous development by Lvov [15] and Massmann [16] however, the first application of one such device to a... [Pg.348]


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Developing chambers

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