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Dished electrode cell

Many such processes continue to use parallel plate reactors, a number of which are now available for purchase (e.g. the SU cell[37], the dished electrode cell[38] and the FM21 cell[22]) but many syntheses fail to be applied because economic assessments are based on unnecessarily complex designs and expensive cell components developed for other application e.g. membranes, Ti cell bodies, electrode materials. Hence it is particularly good to see the development and application of very cheap configurations, for example the new Monsanto process[24] or the Swiss Roll cell[35j. It is to be hoped that more companies give consideration to cell systems specifically designed for particular processes. [Pg.275]

Fl 7.26 A dished-electrode cell stack for use in flue-gas desulphurization. Each cell is undivided and the stack contains 34 cathodes, each of 1 The electrical connections are monopolar with external electrolyte manifolding to each compartment. (Courtesy ... [Pg.381]

Di-sec-butyl percarbonate (SBP), 6 303 Di-sec-butylphenol (DSBP), 2 230 physical properties of, 2 205t 2,4-Di-sec-butylphenol, 2 230 2,6-Di-sec-butylphenol, 2 230 health and safety data, 2 220t N, N -Di-sec- bu tyl-p -pheny lenediamine, 3 108 Dished electrode membrane (DEM) cell, 9 669... [Pg.279]

Hughes, D., 1988, The dished electrode membrane cell facilitates wide range of syntheses, Spec. Chem., 8 16, 17. [Pg.242]

Fig. 2J0 The dished electrode membrane (DEM) cell, (a) Section of the divided unit cell, (b) ScctLOEi of the undivided unit cell, (c) Exploded view of a divided unit cetL (d) An intermediate size reactor, comprising six unit cells, which is used for pilot-plant and small-scale production of, for example, pharmaceuticals, A larger cell stack, incorporating 34 unit cells is shown in Fig. 7.26. (Courtesy Electricity Council Research Centre)i... Fig. 2J0 The dished electrode membrane (DEM) cell, (a) Section of the divided unit cell, (b) ScctLOEi of the undivided unit cell, (c) Exploded view of a divided unit cetL (d) An intermediate size reactor, comprising six unit cells, which is used for pilot-plant and small-scale production of, for example, pharmaceuticals, A larger cell stack, incorporating 34 unit cells is shown in Fig. 7.26. (Courtesy Electricity Council Research Centre)i...
The Dished Electrode Membrane cell (Fig. 2.30) uses specially shaped electrodes in order to provide a smalt interelectrode gap over the active electrode, while maintaining adequate peripheral space at the bottom and top of the electrodes for a conventional pipe manifold. When bipolar operation is used, the use of relatively long external manifolds (Fig. 2.30(d)) minimizes bypass currents. [Pg.151]

Steetley Engineering Ltd.) (Note The Dished Electrode Membrane cell has recently been acquired by Electrocatalytfc Ltd.)... [Pg.381]

One of the reactors uses the dished electrode membrane concept (section 2.7.3) (Fig. 7.26). It employs thirty-four cathodes, each 1 m in area and fabricated from Hastelloy C276 the plate anodes are DSA (Ru02/Ti02)-coated titanium. The other reactor is a Deutsche Carbone cell, which utilizes graphite anodes and cathodes. [Pg.382]

Polar Cell Systems for Membrane Transport Studies Direct current electrical measurement in epithelia steady-state and transient analysis, 171, 607 impedance analysis in tight epithelia, 171, 628 electrical impedance analysis of leaky epithelia theory, techniques, and leak artifact problems, 171, 642 patch-clamp experiments in epithelia activation by hormones or neurotransmitters, 171, 663 ionic permeation mechanisms in epithelia biionic potentials, dilution potentials, conductances, and streaming potentials, 171, 678 use of ionophores in epithelia characterizing membrane properties, 171, 715 cultures as epithelial models porous-bottom culture dishes for studying transport and differentiation, 171, 736 volume regulation in epithelia experimental approaches, 171, 744 scanning electrode localization of transport pathways in epithelial tissues, 171, 792. [Pg.450]

Such electrodes have been used to examine insulin secretion from single pancreatic P cells. A stimulant is introduced to contact a single P cell adhering to the bottom of a petri dish. The microelectrode is brought into contact with the cell. The result (representing insulin secretion) is shown in Fig 14.45. The peaks shown are Ca2+ dependent, and this is characteristic of an exocytotic process (Section 14.10.1). The area under the peak represents 360,000 insulin molecules. The results show that the spikes correspond to the ejection of packets of insulin secreted in exocytosis. [Pg.465]

The recticulated vitrous carbon is cut into 2mm x I mm X 0.5 mm. A copper connective wire (0.3 mm) with thermoplastic insulation is attached to the RVC by silver epoxy. The silver epoxy is allowed to dry overnight in a vacuum oven (70 C) and is then insulated by nonconductive epoxy. The polymeric film is deposited from a degased solution of monomeric porphyrin using the same procedure as described for the preparation of a single-fiber sensor. After film formation, the electrode is dried in a vacuum oven at 40 C and then dip-coated in 1% Nafion in alcohol. The biological cells suspended in 3 ml culture medium are placed dropwise onto the sensor (sterilized by UV light) located in a 60 x 15 mm tissue culture dish. The concentrated cell suspension on the sen.sor is incubated for approxi-... [Pg.246]

From electrochemistry, our discipline has borrowed important terminology. One electrode with electrolyte is called a half-cell to underline that one electrode is not enough. Two electrodes, an electrode pair, are needed to close the electric circuit so that electric current can flow (CC electrodes). A whole cell is two electrodes both submerged in the same electrolyte (e.g., in a glass dish). [Pg.219]

Fig. 8. Labeling the endoderm of 7.0-d embryo by electroporation. A The embryo is first bathed in plasmid DNA solution before transfer to the electroporation drop on the culture dish. To electroporate the distal tip, the embryo is held at the extraembryonic ectoderm by suction using the holding pipet (hp) and positioned between the platinum plate (cathode) and tungsten needle (anode). The electrodes are connected to an Electro Square Porator and the electroporation is focused at the tissue closest to the needle tip. B Fluorescent cells in the distal region of the embryo following electroporation with a P-actin-eGFP construct and cultured for 3h. Fig. 8. Labeling the endoderm of 7.0-d embryo by electroporation. A The embryo is first bathed in plasmid DNA solution before transfer to the electroporation drop on the culture dish. To electroporate the distal tip, the embryo is held at the extraembryonic ectoderm by suction using the holding pipet (hp) and positioned between the platinum plate (cathode) and tungsten needle (anode). The electrodes are connected to an Electro Square Porator and the electroporation is focused at the tissue closest to the needle tip. B Fluorescent cells in the distal region of the embryo following electroporation with a P-actin-eGFP construct and cultured for 3h.
Thermal functionalization methods make up the majority of methods reported in the literature for Si-C bond formation on porSi (Tables 1,2,3,4,5, and 6). The procedures are quite straightforward samples can be placed in small flask or vial (Fig. 2a), immersed in or coated with the reactant, and heated (if required). If a vial is used, the cap should be lined with material that is inert to the vapors from the liquid. For electrochemical functionalization methods (Table 7), use of the same etching cell setup used originally to prepare the porSi works well (Fig. 2b). The electrolyte/reactant and electrode (usually Pt) are placed within the well above the porSi wafer. The wafer sits on a rectangular aluminum electrode, which in Fig. 2b was cut from a weighing dish. [Pg.826]

Fig. 3.9 Lc/t High-temperature-high-pressure electrochemical wall-tube cell (A) inlet, (B) pre-cell, (C) mixing dishes, (D) platinum resistor, (E) reference electrode, (F) counter electrode, (G) zircaloy nozzle, (H) outlet, (I) working electrode, (J) cell and (K) zircaloy rings. Right Typical voltammograms in Fe /Fe 1 mM in 0.2 M Na2S04 (pH 1.5) on a platinum electrode at 85 °C. Sweep rate 50 mV s, H 0.264 cm, d 0.204 cm and = 0.05 cm. Flow rates (a) 4, (b) 8, (c) 12 and (d) 20 cm min. From [259], with permission... Fig. 3.9 Lc/t High-temperature-high-pressure electrochemical wall-tube cell (A) inlet, (B) pre-cell, (C) mixing dishes, (D) platinum resistor, (E) reference electrode, (F) counter electrode, (G) zircaloy nozzle, (H) outlet, (I) working electrode, (J) cell and (K) zircaloy rings. Right Typical voltammograms in Fe /Fe 1 mM in 0.2 M Na2S04 (pH 1.5) on a platinum electrode at 85 °C. Sweep rate 50 mV s, H 0.264 cm, d 0.204 cm and = 0.05 cm. Flow rates (a) 4, (b) 8, (c) 12 and (d) 20 cm min. From [259], with permission...

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See also in sourсe #XX -- [ Pg.275 ]

See also in sourсe #XX -- [ Pg.105 ]




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