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Gels additional preparation technique effect

As long ago as 1946, Consden, Gordon and Martin [137] carried out electrophoretic separation of a mixture of amino acids and peptides on a thin layer of silica gel. Although this technique was accompanied by no particular difficulties, it could not at first keep up with the development at the same time of paper electrophoresis, which was so extremely simple to carry out [129, 268, 777]. Only in recent years, after Stahl in fundamental work had shown how to prepare and use thin layers of adsorbent, has the idea of thin-layer electrophoresis been taken up again. It has the advantage over paper electrophoresis, that interfering adsorption effects can often be avoided through appropriate choice of adsorbent the scope of the method can thus be markedly broadened. In addition, the more uniform and finer structure of the adsorbent used for thin-layer electrophoresis, compared with filter paper, sometimes leads to better resolution. [Pg.105]

Elastin-mimetic protein polymers have been fabricated into elastic networks primarily via y-radiation-induced, radical crosslinking of the material in the coacervate state [10]. Although effective, this method cannot produce polymers gels of defined molecular architecture, i.e., specific crosslink position and density, due to the lack of chemoselectivity in radical reactions. In addition, the ionizing radiation employed in this technique can cause material damage, and the reproducibility of specimen preparations may vary between different batches of material. In contrast, the e-amino groups of the lysine residues in polymers based on Lys-25 can be chemically crosslinked under controllable conditions into synthetic protein networks (vide infra). Elastic networks based on Lys-25 should contain crosslinks at well-defined position and density, determined by the sequence of the repeat, in the limit of complete substitution of the amino groups. [Pg.125]

The molecular size distributions and the size-distribution profiles for the nickel-, vanadium-, and sulfur-containing molecules in the asphaltenes and maltenes from six petroleum residua were determined using analytical and preparative scale gel permeation chromatography (GPC). The size distribution data were useful in understanding several aspects of residuum processing. A comparison of the molecular size distributions to the pore-size distribution of a small-pore desulfurization catalyst showed the importance of the catalyst pore size in efficient residuum desulfurization. In addition, differences between size distributions of the sulfur- and metal-containing molecules for the residua examined helped to explain reported variations in demetallation and desulfurization selectivities. Finally, the GPC technique also was used to monitor effects of both thermal and catalytic processing on the asphaltene size distributions. [Pg.139]

In order to determine the effect of sample preparation and sphere size on the transport properties of PrjOia -, Iwo additional series of experiments were made. In the first, spheres prepared by the sol-gel technique were used. These were annealed at 875°C with frequent changes of oxygen atmosphere until CO2 was no longer observed to be evolved this required one week. In... [Pg.263]

Recently, a fume pyrolysis with the sol-gel technique was examined to prepare aluminum oxide powders from boehmite sol suspension derived from Al-alkoxide. Aluminum oxide was spherical shape and crude structure. In addition, the aluminum oxide possessed a high thermal resistance at 1473K as high as 50 m g- l in surface area[5]. The fume pyrolysis method was also an effective preparation for thin films composed of mixed oxides because one of the advantages is that the atomic composition in source solution is the same as the formed oxide particles. A Yi Ba2Cu307.x film was successfully prepared[6]. These suggest that the combination of the fume pyrolysis and the sol-gel method seem to be an interesting preparation method. [Pg.320]


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See also in sourсe #XX -- [ Pg.34 , Pg.281 ]




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Addition techniques

Additive techniques

Preparation techniques

Preparative techniques

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