Oxidative gelation

An ink is considered dry when a print does not stick or transfer to another surface pressed into contact with it. Drying is accompHshed by one or more of the following physical or chemical mechanisms absorption, evaporation, precipitation, oxidation, polymerization, cold setting, gelation, and radiation curing. 

For binder preparation, dilute hydrochloric or acetic acids are preferred, because these faciUtate formation of stable silanol condensation products. When more complete condensation or gelation is preferred, a wider range of catalysts, including moderately basic ones, is employed. These materials, which are often called hardeners or accelerators, include aqueous ammonia, ammonium carbonate, triethanolamine, calcium hydroxide, magnesium oxide, dicyclohexylamine, alcohoHc ammonium acetate, and tributyltin oxide (11,12). 

The most important role of UO3 is in the production of UF4 [10049-14-6] and UF [7783-81-5], which are used in the isotopic enrichment of uranium for use in nuclear fuels (119—121). The trioxide also plays a part in the production of UO2 for fuel peUets (122). In addition to these important synthetic appHcations, microspheres of UO3 can themselves be used as nuclear fuel. Fabrication of UO3 microspheres has been accompHshed using sol-gel or internal gelation processes (19,123—125). FinaHy, UO3 is also a support for destmctive oxidation catalysts of organics (126,127). 

Uranium and mixed uranium—plutonium nitrides have a potential use as nuclear fuels for lead cooled fast reactors (136—139). Reactors of this type have been proposed for use ia deep-sea research vehicles (136). However, similar to the oxides, ia order for these materials to be useful as fuels, the nitrides must have an appropriate size and shape, ie, spheres. Microspheres of uranium nitrides have been fabricated by internal gelation and carbothermic reduction (140,141). Another use for uranium nitrides is as a catalyst for the cracking of NH at 550°C, which results ia high yields of H2 (142). 

Properties. MethylceUulose [9004-67-5] (MC) and its alkylene oxide derivatives hydroxypropylmethylceUulose [9004-65-3] (HPMC), hydroxyethylmethylceUulose [9032-42-2] (HEMC), and hydroxybutyknethylcellulose [9041-56-9] (HBMC) are nonionic, surface-active, water-soluble polymers. Each type of derivative is available in a range of methyl and hydroxyalkyl substitutions. The extent and uniformity of the methyl substitution and the specific type of hydroxyalkyl substituent affect the solubifity, surface activity, thermal gelation, and other properties of the polymers in solution. 

The commercial polymers are of comparatively low molecular weight (M = 25 000-60 000) and whilst being essentially linear may contain a few branches or cross-links arising out of thermal oxidation. Exposure to ultraviolet light causes a rapid increase in gel content, whilst heating in an oven at 125°C causes gelation only after an induction period of about 1000 hours. Eor outdoor applications it is necessary to incorporate carbon black. The polymers, however, exhibit very good hydrolytic stability. 

Rombouts, F.M. and Thibault, J.F. (1986) Sugar beet pectins chemical structure and gelation through oxidative coupUng. In Chemistry and Function of Pectins, edited by M.L. Fishman, et al, pp. 49-60. American Chemical Society, Washington, DC. 

The cement sets as the result of an acid-base reaction between a zinc oxide dental powder and a poly(alkenoic acid). The pH increases and an insoluble amorphous salt is formed which acts as the cement matrix. A general account of the gelation processes is given in Section 5.4. 

Micard V and Thibault JF. 1999. Oxidative gelation of sugar-beet pectins use of laccases and hydration properties of the cross-linked pectins. Carbohyd Polym 39 265-273. 

Figure 20. Spectroelectrochemical analysis of thin films of V2O5 ambigels supported on conductive glass (indium—tin oxide). The current response is given by the continuous line, and the change in absorbance monitored at 400 and 800 nm as a function of potential (and time) is shown as individual data points. The V2O5 ambigel was prepared by gelation of aqueous metavanadate, dried from cyclohexane, and calcined in air at 170 °C. (Printed with permission from ref 232.)...

Metal oxide nanotubes have been synthesized by a diverse variety of fabrication routes. For example titania nanotubes, and nanotube arrays, have been produced by deposition into a nanoporous alumina template [48-51], sol-gel transcription using organo-gelators as templates [52,53], seeded growth [54], hydrothermal processes [55-57] and anodic oxidation [58-65]. 

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