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Timing thinning

Crude methyl 2-bromostearate (33 g, 0 087 mol) is dissolved in 200 mL of acetonitrile containing 0 5 mL of water, and silver(I) fluonde (50 g, 0 393 mol) is added rapidly in one portion The slurry is stirred vigorously for 20 h in an oil bath at 80 C At the end ot this time thin-layer chromatographic analysis (petroleum... [Pg.195]

In earlier times, thin-layer chromatography (TLC), polyamide chromatography, and paper electrophoresis were the major separation techniques for phenolics. Of these methods, TLC is still the workhorse of flavonoid analysis. It is used as a rapid, simple, and versatile method for following polyphenolics in plant extracts and in fractionation work. However, the majority of published work now refers to qualitative and quantitative applications of high-performance liquid chromatography (HPLC) for analysis. Llavonoids can be separated. [Pg.1]

A mixture of 3.44 g (9.63 mmoles) of 4-(2-di-n-propylaminoethyl)-7-hydroxy-2(3H)-indolone hydrobromide (U. S. Pat. No. 4,314,944), 22 cc of dimethylformamide, 1.79 g (9.91 mmoles) of 5-chloro-l-phenyl-lH-tetrazole, 220 cc of acetone, 10 cc of water and 2.90 g (21 mmoles) of anhydrous potassium carbonate was refluxed for about 3 hours at which time thin layer chromatographic analysis (silica gel GF, 75-23-2 ethyl acetate-methanol-conc. ammonium hydroxide) indicated that the reaction was complete. [Pg.3001]

Flexible >2 Bend many times Thin, bendable, lightweight, rugged... [Pg.345]

The presence of these spontaneously adsorbed (i.e. adsorbed during minimum exposure times), thin films on polymeric substrates such as polystyrene culture dishes and glass plates usually cannot be demonstrated by other spectroscopic methods. For example, the modified internal reflection spectroscopic technique, in which an auxiliary salt prism (usually the malleable salt KRS-5) is pressed against the demonstrably (by other techniques) protein-coated substrates, always fails this technique is not sensitive enough for the near monolayer ranges required for this demonstration. The required sensitivity is achieved only when adsorption occurs directly on the face of a clean, or thin film-coated, internal reflection element. [Pg.303]

The first techniques yields good optical quality thin films with thickness controlled by the deposition time. Thin films with thickness varying from ca. 100 to 1000 nm were easily obtained. The conditions for thin film deposition were as follows ... [Pg.614]

Radiation damage may also occur from exposure to the skin. Medically, radioactive strontium probes have been used intentionally to destroy unwanted tissue on the surface of the eye or skin. The eye tissues sometimes become inflamed or abnormally thin after a long time. Thinning of the lower layer of the skin (dermis) has also been reported in animal studies as a delayed effect. In addition, skin and bone cancer were reported in animals that were irradiated on the skin by exposure to a radioactive strontium probe. [Pg.25]

If the gel layer is not the limiting resistance to flow, the layer will continue to grow until the channel is completely full of 75% solid material-resulting in a drop in recirculation rate with time. Thin channel tubes and spiral flow modules running continuously at constant latex feed concentration and pressure drop for periods approaching one year have shown no decreases in recirculation rate or accumulation of polymer latex in the channels. [Pg.186]

There has been a close interrelation between glass and thin films for a long time. Thin films on glass are used both for scientific and industrial purposes. One of the most important requirements placed on industrial coatings is that they adhere well to the substrate surface, particularly if they are to be subjected to extreme environmental conditions. This topic is treated in Chapter 5. [Pg.563]

The three characteristic lengths are reactor length and diameter and the mean particle diameter of the solid bed. Long and at the same time thin tubes should be given preference. This is not exactly a new finding. It has influenced equipment design already for many years and led to today s design of tube bundle reactors. [Pg.145]

At the same time, thin-layer series electrodes were being developed for microbore LCEC (Goto et ai, 1981, 1982). With flow rates of 10-100 //1/min, the arrangement could provide 100% conversion efficiency at each sensor. An automated-trace-enrichment, tandem column system was devised for the direct injection of urine samples containing catecholamines (Fig. 33 A). Samples were injected onto an activated aluminum oxide microbore column with a pH 8.8 Tris buffer. The alumina column was then coupled with the reversed-phase microbore analytical column the catechols were eluted using pH 1.8 mobile phase. The downstream electrode was monitored (Fig. 33B). [Pg.237]

To investigate the long-term stability of the conductivity of PPy-DBSA, PPy films of about 0.1 p,m thickness were prepared using chloroform with extra DBSA and the film resistivity was monitored with elapsed time. Thin PPy-DBSA films should be used to investigate the stability since the conductivity of thick films tends to be insensitive to their chemical degradation, which results from the slow diffusion of oxygen into the thick PPy-DBSA film. [Pg.298]

In the same year Izmailov and Shraiber [6] utilized for the first time thin layer chromatography. [Pg.11]

In 1941, Crowe [140], quoting this and other earlier publications, reported that his team had been using for some time thin layers of adsorbents in Petri dishes and, with this technique, had been able to ascertain rapidly the suitable solvent for elution in column chromatography. [Pg.1]

An electrode of a given geometry may be equipped with different types of membranes and thus optimized for applications requiring either maximum mechanical and long-term stability or fast response time. Thin Teflon membranes provide fast response but low mechanical stability and vice versa. [Pg.403]

Thin films of prepared nanocomposite were made using a hot press (230°C and 30s pressing time). Thin films were cut into pieces and washed with hot water to remove any uiueacted species present in the polymer. [Pg.388]


See other pages where Timing thinning is mentioned: [Pg.330]    [Pg.142]    [Pg.90]    [Pg.191]    [Pg.208]    [Pg.351]    [Pg.457]    [Pg.821]    [Pg.143]    [Pg.330]    [Pg.566]    [Pg.140]    [Pg.2]    [Pg.208]    [Pg.566]    [Pg.118]    [Pg.271]    [Pg.122]    [Pg.278]    [Pg.1038]    [Pg.14]    [Pg.393]    [Pg.10]    [Pg.1342]    [Pg.337]    [Pg.35]    [Pg.210]    [Pg.305]    [Pg.18]   
See also in sourсe #XX -- [ Pg.99 , Pg.100 , Pg.104 ]




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