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Dipping sequences

Ehrlich p-Dimethylaminobenzaldehyde (100 g l"1) in cone. HC1. Mix 1 volume with 4 volumes of acetone. No heat required. Reacts within 20 min Trp Citrulline Pink/red Yellow Some indoles, aromatic amines and ureides react. Use after ninhydrin in multiple-dip sequences... [Pg.369]

Other reagents that are more specific for particular amino acids have been described (Table 10.8) and their use significantly assists in the identification process. The different locating reagents may be applied either to separate chromatograms or as part of a multi-dip sequence, when they should be used in the recommended order to prevent interference of one reagent by another. Many reagents are hazardous and must be handled in accordance with approved safety procedures. [Pg.370]

Figure 4.3. To maintain a constant surface pressure during the deposition process, the area enclosed by the barrier is reduced systematically. This schematic Y-type dipping sequence for a diagram shows a staircase structure of 4, 8, 12, and 16 monolayers. Courtesy of Joyce-Loebl Company, Gateshead, England.)... Figure 4.3. To maintain a constant surface pressure during the deposition process, the area enclosed by the barrier is reduced systematically. This schematic Y-type dipping sequence for a diagram shows a staircase structure of 4, 8, 12, and 16 monolayers. Courtesy of Joyce-Loebl Company, Gateshead, England.)...
Fmther support for the role of hydrophobic interactions in the area-selective adsorption was obtained by reversing the dipping sequence. A single bilayer was adsorbed on a methyl- and hydroxyl-terminated stripe pattern (10 and 5 pm, respectively), in one case starting with the polycation, in the other case with first adsorbing the polyanion. Both substrates were subsequently analyzed by AFM in contact mode. The friction force images (Fig. 8) clearly show a reversal in contrast for both experiments, compared with the template without the polymers, indicating that in both cases one bUayer had been deposited selectively on the methyl-terminated areas. [Pg.110]

Figure 5.1. Schematic of the Langmuir-Blogett deposition process. The amphiphile is dissolved in an organic solvent and subsequently spread at the air-water interface. The solvent evaporates and a monolayer of the amphiphile at the air-water interface remains (a). The monolayer at the air-water interface can be further manipulated by means of a movable barrier allowing control of the area per molecule (b). The Langmuir monolayer can be transferred by an up-stroke on to a hydrophilic surface (c) and via a down-stroke on to a hydrophobic surface. A dual compartment trough enables the simultaneous processing of two different materials (d), while a programmed dipping sequence allows the determination of layer architecture at a molecular level... Figure 5.1. Schematic of the Langmuir-Blogett deposition process. The amphiphile is dissolved in an organic solvent and subsequently spread at the air-water interface. The solvent evaporates and a monolayer of the amphiphile at the air-water interface remains (a). The monolayer at the air-water interface can be further manipulated by means of a movable barrier allowing control of the area per molecule (b). The Langmuir monolayer can be transferred by an up-stroke on to a hydrophilic surface (c) and via a down-stroke on to a hydrophobic surface. A dual compartment trough enables the simultaneous processing of two different materials (d), while a programmed dipping sequence allows the determination of layer architecture at a molecular level...
Combination tra/ s—sedimentary trap features that result from both stratigraphic and structural mechanisms. There can be many combinations for stratigraphic and structural traps. An example of such a trap would be a reef feature overlaying a porous and permeable sandstone, but in which the sequence has been faulted (see Figure 2-54). Without the fault, which has provided an impregnable barrier, the hydrocarbons would have migrated further up dip within the sandstone. [Pg.254]

Sheet steel is normally prepared for application of enamel by a sequence of operations including thorough degreasing, acid pickling and neutralisation. A nickel dip stage is often included to deposit a thin, porous layer of nickel applied at about 1 g/m especially when conventional groundcoat is not used (see Section 13.7). [Pg.737]

FIG. 20 SEM pictures of particle assemblies after different numbers of alternating dipping steps into dispersions of anionic particles lb and cationic particles 2 beginning with lb. A glass substrate modified with 3-AMDS was used and dipped with sequence (a) lb only, (b) lb-2, (c) lb-2-lb, (d) (lb-2) X 2, (e) (lb-2) X 3, (f) (lb-2) X 5. (From Ref. 93, with permission from Elsevier, Amsterdam.)... [Pg.236]

The previous analysis indicates that although the voltammetiic behavior suggests that the aqueous phase behaves as a metal electrode dipped into the organic phase, the interfacial concentration of the aqueous redox couple does exhibit a dependence on the Galvani potential difference. In this sense, it is not necessary to invoke potential perturbations due to interfacial ion pairing in order to account for deviations from the Butler Volmer behavior [63]. This phenomenon has also been discarded in recent studies of the same system based on SECM [46]. In this work, the authors observed a potential independent ket for the reaction sequence. [Pg.209]

Each beaker held the PEM film for one hour in sequence. Use safety glasses and gloves while working with the solutions. The sequence of beakers used to dip the PEM was set up as follows ... [Pg.2]

The successes of hydrophilicity scales in correlating much data mean that one should not underestimate the importance of gs(dip). A plot of AHf (heat of formation of metal oxide, a measure of hydrophilicity) versus X(M) - X(Hg) shows two lines. Preferential orientation increases with oxygen affinity. Correlations between A Hf and X(M) - X(Hg) exist also for solvents other than water, with the rate of increase of X(M) - X(Hg) with A/f/being stronger in the sequence acetonitrile < H20 < DMSO, with increasing... [Pg.63]

Fig. 2. Li abundance in main-sequence and turnoff stars in the open cluster IC 4651 aged of 1.5-1.7 Gyr vs Teff from photometry (open points and triangles for actual determination and upper limits respectively). Black points show rotating model predictions (CT99 and Palacios et al. 2003) at 1.5 Gyr for an initial rotation velocity of 110 km.sec-1 and for various stellar masses. For 1.5Mq models for an initial rotation of 50 and 150 km.sec-1 are also shown (black triangle and square). This provides an estimate of the expected dispersion for stars inside the Li dip. See Pasquini et al. (2004) for more details... Fig. 2. Li abundance in main-sequence and turnoff stars in the open cluster IC 4651 aged of 1.5-1.7 Gyr vs Teff from photometry (open points and triangles for actual determination and upper limits respectively). Black points show rotating model predictions (CT99 and Palacios et al. 2003) at 1.5 Gyr for an initial rotation velocity of 110 km.sec-1 and for various stellar masses. For 1.5Mq models for an initial rotation of 50 and 150 km.sec-1 are also shown (black triangle and square). This provides an estimate of the expected dispersion for stars inside the Li dip. See Pasquini et al. (2004) for more details...
The first electrodeposition of a compound superlattice appears to have been by Rajeshwar et al. [219], where layers of CdSe and ZnSe were alternately formed using codeposition in a flow system. That study was proof of concept, but resulted in a superlattice with a period significantly greater then would be expected to display quantum confinement effects. There have since been several reports of very thin superlattices formed using EC-ALE [152, 154, 163, 186], Surface enhanced Raman (SERS) was used to characterize a lattice formed from alternated layers of CdS and CdSe [163]. Photoelectrochemistry was used to characterize CdS/ZnS lattices [154, 186]. These EC-ALE formed superlattices were deposited by hand, the cycles involving manually dipping or rinsing the substrate in a sequence of solutions. [Pg.56]

Step 4 After rinsing, dip both ends of the capillary and the electrodes for approximately 5 s in two separate vials fully filled with background electrolyte. (This is needed to wash out potential crystalline salt/ particles in order to avoid spikes and current cuts due to arching.) The same set of dip-vials are used throughout a sequence. [Pg.72]


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See also in sourсe #XX -- [ Pg.90 ]




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Dipping

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