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Ultra-thin layers

The latest innovation is the introduction of ultra-thin silica layers. These layers are only 10 xm thick (compared to 200-250 pm in conventional plates) and are not based on granular adsorbents but consist of monolithic silica. Ultra-thin layer chromatography (UTLC) plates offer a unique combination of short migration distances, fast development times and extremely low solvent consumption. The absence of silica particles allows UTLC silica gel layers to be manufactured without any sort of binders, that are normally needed to stabilise silica particles at the glass support surface. UTLC plates will significantly reduce analysis time, solvent consumption and increase sensitivity in both qualitative and quantitative applications (Table 4.35). Miniaturised planar chromatography will rival other microanalytical techniques. [Pg.226]

Teramura Y, Kaneda Y, Iwata H (2007) Islet-encapsulation in ultra-thin layer-by-layer membranes of poly(vinyl alcohol) anchored to poly(ethylene glycol)-lipids in the cell membrane. Biomaterials 28 4818 -825... [Pg.199]

It should be noted here that the ultra thin-layer cells (UTLC) which result from the close approach of an STM tip to a conducting substrate may have important electroanalytical applications in studies other than STM imaging (64). This is because extremely large current densities should be attainable in such cells, and also because of the fast transit times (e.g., 50 nsec for d - 10 nm) for reactants across the cell. Thus, such UTLC s might facilitate the determination of fast heterogeneous rate constants or the study of reactive electrochemical intermediates (64). [Pg.184]

The fifth contribution by M. Putkonen and L. NiinistO presents an overview of Organometallic Precursors for Atomic Layer Deposition (ALD). The key principle of ALD in contrast to CVD is the exclusion of any gas-phase prereaction allowing the thin film growth to be fully controlled by surface reactions and adsorption/desorption kinetics. ALD is thus ideally suited for the growth of ultra-thin layers and atomically abrupt interfaces needed in future nanoelectronic devices. While CVD and ALD have many aspects in common, precursors suitable for ALD generally need to be much more reactive than those used for CVD. Another challenge is to combine low steric demand with very high selectivity of the surface reactions. [Pg.223]

A typical silicon PV cell is composed of a wafer consisting of an ultra-thin layer of phosphorus-doped silicon (N-layer with a negative character). [Pg.87]

Thin to Ultra Thin Layers of Chalcogenide Materials... [Pg.142]

The novel cluster-like chalcogenide material RuxSey deposited in thin [5, 26, 31, 36] and ultra-thin layers [9, 11] or in powder form embedded in a polymer matrix [30] was found to be an efficient catalyst for the molecular oxygen reduction in acid medium. Fig. 5.10 summarizes the current-potential (j-E) characteristics as a function of the substrate s nature. First of all, one can appreciate that similar activities are obtained from materials synthesized in powder or in colloidal form when deposited onto GC (Fig. 5.10, compare curves (1) and (2)). For the sake of comparison, the j-E characteristic generated on the naked GC substrate for the electrochemical process is contrasted in curve (5). [Pg.144]

Fig. 5.10. The electrochemical activity (Tafel plots) of surface modified by RuxSey towards the molecular oxygen reduction in 0.5M H2SO4. (1) layer deposited during the synthesis of powder on glassy carbon (GC) (2) ultra thin layer deposited via colloidal solution on glassy carbon (3) ultra thin layer deposited via colloidal solution on Sn02 F (FTO) (4) ultra thin layer deposited via colloidal solution on Ti02 (anatase) supported on FTO (5) the electrochemical response of naked GC. All systems (2 to 4) were annealed in argon at 210°C to eliminate the stabilizer (octadecanthiol). TL Thin layer UTL Ultra thin layer of RuxSey. Fig. 5.10. The electrochemical activity (Tafel plots) of surface modified by RuxSey towards the molecular oxygen reduction in 0.5M H2SO4. (1) layer deposited during the synthesis of powder on glassy carbon (GC) (2) ultra thin layer deposited via colloidal solution on glassy carbon (3) ultra thin layer deposited via colloidal solution on Sn02 F (FTO) (4) ultra thin layer deposited via colloidal solution on Ti02 (anatase) supported on FTO (5) the electrochemical response of naked GC. All systems (2 to 4) were annealed in argon at 210°C to eliminate the stabilizer (octadecanthiol). TL Thin layer UTL Ultra thin layer of RuxSey.
The solution has a black color and is very stable with time, even if exposed to air. The observed spectrum is rather broad with a maximum peak centered at 351 nm. Its morphology is depicted in Fig. 5.5(b). Such featureless spectrum has also been observed with reduced Pd colloid solution [56]. Comparing the optical absorption of Ti02 colloidal diluted solutions, prepared from P25 Degussa RuxSey ultra thin layers can produce charge... [Pg.146]

The aim of this chapter is to cover the theoretical and practical aspects of capillary gel electrophoresis. It also provides an overview of the key application areas of nucleic acid, protein, and complex carbohydrate analysis, affinity-based methodologies, as well as related microseparation methods such as ultra-thin-layer gel electrophoresis and electric field-mediated separations on microchips. It also gives the reader a better understanding of how to utilize this technology, and determine which actual method will provide appropriate technical solutions to problems that may have be perceived as more fundamental. Micropreparative aspects and applications are discussed in Chapter 12. [Pg.70]

Ultra-thin-layer gel electrophoresis is a combination of slab-gel electrophoresis and capillary gel electrophoresis [130], providing a multilane separation plat-... [Pg.96]

In addition to the use of conventional preseparation labeling, ultra-thin-layer gel electrophoresis systems readily accommodate fluorophore labeling dur-... [Pg.97]

Isoelectric focusing and electrophoresis were used for protein mapping and to study protein extraction in horizontal ultra-thin-layer format [138], The 0.12-0.36-mm-thick polyacrylamide gel layer was deposited onto tiny glass plates (e.g., microscope slides). The method enabled the analysis of 1-ng tissue culture specimens. Ultra-thin-layer polyacrylamide isoelectric focusing gel was also employed in two-dimensional analysis of plant and fungal proteins. Marlow et al. [139] reported on the use of 0.2-mm semirigid backing (polyester)-supported... [Pg.98]

Automated ultra-thin-layer gel electrophoresis was applied for large-scale analysis of SDS-protein complexes and for molecular-mass estimation of the proteins in the sample [12], Figure 13 compares the separations of two differ-... [Pg.99]

Fig. 21.3. Schematic figure of iton-covalent imprinting of polyurethane with an organic solvent as template and porogen. Highly robust MIPs are best prepared over night at room temperature. Template removal is achieved by evaporation or dissolution. Due to the ultra-thin layers the print molecules are often removed completely. Fig. 21.3. Schematic figure of iton-covalent imprinting of polyurethane with an organic solvent as template and porogen. Highly robust MIPs are best prepared over night at room temperature. Template removal is achieved by evaporation or dissolution. Due to the ultra-thin layers the print molecules are often removed completely.
Szoke M, Sasvari-Szelely M, Guttman A. Ultra-thin-layer agarose gel electrophoresis, I. Effect of the gel concentration and temperature on the separation of DNA fragments. J Chromatog A 1999 830 465-71. [Pg.140]


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See also in sourсe #XX -- [ Pg.157 ]




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