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Wet cells

One of the main uses of these wet cells is to investigate surface electrochemistry [94, 95]. In these experiments, a single-crystal surface is prepared by UFIV teclmiqiies and then transferred into an electrochemical cell. An electrochemical reaction is then run and characterized using cyclic voltaimnetry, with the sample itself being one of the electrodes. In order to be sure that the electrochemical measurements all involved the same crystal face, for some experiments a single-crystal cube was actually oriented and polished on all six sides Following surface modification by electrochemistry, the sample is returned to UFIV for... [Pg.314]

Nasae,/. wetness, moisture, humidity. Nass-echtheit, /. fastness to wetting or wet processing, -element, n. (Elec.) wet cell, wet battery. [Pg.313]

An amount of enzyme preparation equivalent to 900 mg of wet cells was made up to 25 ml with the above potassium phosphate buffer solution. 150 mg (1.15 mmol) of 5-fluorouracil and 1.0 gram of thymidine (4.12 mmol) were dissolved in 15 ml of the above potassium phosphate buffer solution. The mixture was incubated at 37°C for 18 hours. After this time, enzyme action was stopped by the addition of four volumes of acetone and one volume of peroxide-free diethyl ether. The precipitated solids were removed by filtration, and the filtrate was evaporated under nitrogen at reduced pressure until substantially all volatile organic solvent had been removed. About 20 ml of aqueous solution, essentially free of organic solvent, remained. This solution was diluted to 100 ml with distilled water. [Pg.651]

Cultures of G. polyedra (L. polyedrum) are grown at 20 5°C in a supplemented sea water medium (Hastings and Sweeney, 1957 Hastings and Dunlap, 1986), under cool-white fluorescent lighting of a 12-hr light/12-hr dark cycle. The cultures are inoculated at densities of 100 to 500 cells/ml. After 2-4 weeks, cells are harvested by vacuum filtration on a filter paper at cell densities of 7,000-15,000 cells/ml, yielding 0.3-0.7 g wet cells per liter of culture. [Pg.251]

Isolated polynucleotide clusters from Rhodococcus opacus which encode four polypeptides possessing the activities of a NHase (a and /3 subunits), an auxiliary protein P15K that activates the NHase, and a cobalt transporter protein were expressed in Escherichia coli DSM 14459 cells [34]. Methionine nitrile was added continuously to a suspension of the transformant cells (5.6% w/v of wet cells) in phosphate buffer (50 mM, pH 7.5) at 20 °C, at a rate where the nitrile concentration did not exceed 15 g L 1 while maintaining the pH constant at 7.5. After 320 min, the nitrile was completely converted into amide, corresponding to a final product concentration of 176 gL1.4-Methylthio-a-hydroxybutyramide is readily hydrolyzed with calcium hydroxide, where the calcium salt of 4-methylthio-a-hydroxybutyric acid (MHA) can be directly used as a nutritional supplement in animal feed as an alternative to methionine or MHA. [Pg.174]

Zinc metal is very reactive chemically. Zinc metal strips are often used as the plates in wet cell batteries. Galvanized iron is iron that has been coated with a thin film of zinc metal to protect it from corrosion. Many garbage cans and metal buckets are made of galvanized iron. [Pg.60]

For design of a simple manufacturing process, the thermostability of the NP enzymes is a very useful feature. Although heat treatment can be used as part of a purification protocol to isolate the enzymes from contaminating materials, the high temperature of operation itself excludes undesired enzyme-catalysed side reactions. For example, in the synthesis of 9-p-D-arabinofuranosyladenine from Ara-U and adenine, using a wet cell paste of Enterobacter aerogenes, adenine and Ara-U mainly underwent deamination at lower temperatures to form hypoxanthine and uracil respectively. At elevated temperature, deamination was completely eliminated and the rate of transarabinosylation increased. [Pg.32]

The wet cell pellet (7-8 g) obtained was stored at 20 °C until it was used for asymmetric reduction. [Pg.292]

Wet cell pellets were then used directly in Procedure 2 (Section 11.1.2). [Pg.320]

Whole wet cells ( 440 mg) expressing the MAO-N-D5 variant enzyme were suspended in 0.1 M potassium phosphate buffer pH 7.6 (2.46 mL). Racemic crispine A (6.0 mg, 0.03 mmol) was added to this suspension followed by ammonia-borane (3.5 mg, 0.11 mmol). The vial was sealed with the stopper and the mixture was incubated at 30 °C, 250 rpm and samples (0.5 mL) taken periodically for analysis. [Pg.321]

These authors also report a comparison of the efficacy of wet cells compared with heat-dried cells and with Pichia extracts. This appears to show the best result with the extracts, but it is difficult to assess the meaning of this study. The outcome is reported in terms of percentage yield of the final product, and it is impossible to judge whether what is being observed reflects different amounts of activity and incomplete reactions, varying stability of the biocatalyst in its various states, interfering side reactions due to other cellular activities, and so on. It is not clear to what extent reaction under each set of conditions was optimized or maximized. [Pg.77]

Excess tissne flnid may be absorbed with a little gauze, but avoid touching any wet cells. Also, gentle pressure is required, but if too forceful, some cells may be destroyed. [Pg.70]

This picture changed in the 1886 when an American chemist, Charles Martin Hall (1863— 1914), and a French chemist, Paul Louis-Toussaint Heroult (1863—1914), both discovered, at about the same time, a new process for extracting aluminum from molten aluminum oxide by electrolysis. (It might be noted that both discoverers have the same birth and death dates as well as the same date of discovery.) Hall was inspired by his teacher to find a way to inexpensively produce aluminum metal. He wired together numerous wet cells to form a battery that produced enough electricity to separate the aluminum from the melted aluminum oxide (mixed with the minerals cryolyte or fluorite), by the process known as electrolysis. Hall formed the Pittsburgh Reduction Co., which is now known as the Aluminum Company of America, or Alcoa. His company produced so much aluminum that the price dropped to about sixty cents per kilogram. [Pg.180]

Wet cells (15g) in saline (80 ml) are mixed with an equal volume of a 10% w/v monomer solution (85% acrylamide/15% NN methylene bis-acrylamide). Initiator is added (1 ml 5% NNN N -tetramethyldiethylamine and 4 ml 5% ammonium persulphate). Gelation occurs within 20 minutes at 5°C. [Pg.255]

Wet cells (5g) are suspended in 15 ml of a 1% sodium alginate solution. The mixture is then forced through a syringe needle into a 0.05 M CaCl2-solution containing the necessary nutrients for the cell. Gelation occurs almost immediately. [Pg.255]

Studies include wet-cell photoelectrochemical measurements (42,60,72,90), STM measurements on single MS particles in thin films (55,56,81), and conductivity measurements of metal chalcogenides in LB films (20,21,23). Many such studies are driven by the search for cheaper methods and materials for the fabrication of semiconductors suitable for photoelectrochemical devices. Moreover, the ability to tune optical properties via the Q-state effect and the versatility of LB fabrication make the LB films an attractive medium for semiconductor production. The photo-... [Pg.271]

The main task in technical application of asymmetric catalysis is to maximize catalytic efficiency, which can be expressed as the ttn (total turnover number, moles of product produced per moles of catalyst consumed) or biocatalyst consumption (grams of product per gram biocatalyst consumed, referring either to wet cell weight (wcw) or alternatively to cell dry weight (cdw)) [2]. One method of reducing the amount of catalyst consumed is to decouple the residence times of reactants and catalysts by means of retention or recycling of the precious catalyst. This leads to an increased exploitation of the catalyst in the synthesis reaction. [Pg.415]

Fig. 3.1 Leclanche cells, past and present (a) Leclanche wet cell (b) D-si/.e dry cell (Ever Ready) (c) paper battery, (Matsushita Battery Industrial Co.)... Fig. 3.1 Leclanche cells, past and present (a) Leclanche wet cell (b) D-si/.e dry cell (Ever Ready) (c) paper battery, (Matsushita Battery Industrial Co.)...
The original Leclanche cell was a wet cell assembled in a glass jar. The cathode was a carbon rod or plate immersed in a mixture of manganese... [Pg.66]

Fig. 3.30 Cross-section of the electrode assembly of an early 500 Ah mechanically rechargeable zinc-air wet cell used for railway signalling applications... Fig. 3.30 Cross-section of the electrode assembly of an early 500 Ah mechanically rechargeable zinc-air wet cell used for railway signalling applications...

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See also in sourсe #XX -- [ Pg.79 , Pg.81 ]




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