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Temperature reactivity

This low viscosity resin permits cure at low (70°C) temperatures and rapidly develops excellent elevated temperature properties. Used to increase heat resistance and cure speed of bisphenol A epoxy resins, it has utihty in such diverse appHcations as adhesives, tooling compounds, and laminating systems. A moleculady distilled version is used as a binder for soHd propellants (see Explosives and propellants) and for military flares (see Pyrotechnics). Its chief uses depend on properties of low viscosity and low temperature reactivity, particularly with carboxy-terminated mbbers. [Pg.365]

Chemical Reactivity - Reactivity with Water No reaction at ordinary temperatures Reactivity with Common Materials No reaction Stability During Transport Stable Neutralizing Agents for Acids and Caustics Not pertinent Polymerization Not pertinent Inhibitor of Polymerization Not pertinent. [Pg.402]

The reaction of tetraalkyltin complexes with oxide surfaces was studied244,245 but no description at the molecular level has been reported. The low-temperature reactivity of tetraalkyltin (SnR4, where R=Me, Et, i-Pr, Bu) complexes toward the surface of silica was studied in detail.246 At room temperature, the complex is physisorbed. Above 100°C, the adsorbed molecules react with the OH groups and the evolution of alkanes is observed (Scheme 7.15). [Pg.269]

Iron oxide (Fe Oj) and tungsten oxide (WO ) films have been studied and developed as candidate semiconductor materials for the PEC junction (photoanode). High-temperature synthesis methods, as reported for some high-performance metal oxides, have been found incompatible with multijunction device fabricatioa A low-temperature reactive sputtering process has been developed instead. In the parameter space investigated so far, the optoelectronic properties of WO3 films were superior to those of Fe Oj films, which showed high recombination of photogenerated carriers (Miller et al., 2004). [Pg.119]

When high-intensity radiative energy is supplied to the surface of an energetic material, the surface absorbs the heat and its temperature increases. If the energetic material is optically translucent, part of the radiation energy penetrates into the interior of the propellant, where it is absorbed. When the surface reaches its decomposition temperature, reactive gaseous materials are formed on and above the surface through an endothermic or exothermic decomposition reaction. i-2 When the reaction in the gas phase is estabUshed and the temperature is increased... [Pg.369]

B.E.T. apparatus 121), using nitrogen as the adsorbate at liquid nitrogen temperatures. Reactivity data were also determined at a number of other temperatures between 900 and 1350°, but subsequent profile data are lacking. [Pg.179]

V. Aquilanti, S. Cavalli, D. De Fazio, A. Volpi, A. Aguilar, J.M. Lucas, Benchmark rate constants by the hyperquantization algorithm. The F+H2 reaction for various potential energy surfaces Features of the entrance channel and of the transition state, and low temperature reactivity, Chem. Phys. 308 (2005) 237. [Pg.159]

Reaction with H2 and CO Removed even at room temperature, "reactive Not removed, even at 1000 K, "non-reactive ... [Pg.315]

Figure 1. Dyebath reuse 100% cotton/low-temperature reactive dyes... Figure 1. Dyebath reuse 100% cotton/low-temperature reactive dyes...
Table XXVII. Dyebath Reuse Color Difference Calculations 100% Cotton/One Low-Temperature Reactive Dye... Table XXVII. Dyebath Reuse Color Difference Calculations 100% Cotton/One Low-Temperature Reactive Dye...
Long-term dye stability—Low-temperature reactive dyes will slowly hydrolyze with water over long periods of time, even at room temperature. To prevent slow hydrolysis, the dye impregnation bath was kept at a slightly acid pH (- 6.0). This technique proved successful, with dye solutions maintained for several weeks without detectable degradation. [Pg.232]

In the next series of experiments, a procedure incorporating three low-temperature reactive dyes was attempted on 100% cotton. The procedure was modeled after a participating company s formulation. The flow system detailed in Figure 1 was utilized, and the methods developed for the one-dye system were used to attempt shade match with the company standard. Additional problems that arose with the three-dye system were as follows ... [Pg.232]

Good lot-to-lot shade correlations were also obtained with reuse of low-temperature reactive dyebaths and fixation baths on 100% cotton, and with reuse of combined high-energy reactive/disperse dyebaths and fixation baths on cotton/polyester knit fabrics. Further computer program development is required, however, before industrial shades can be matched with the reactive dye reuse system. [Pg.239]

The gaseous reaction of 4 did not occur below 65 °C. Above that temperature, reactivity was indicated by colour changes of the crystalline material from red-purple to white. The reaction could also be monitored by IR spectroscopy, probing the v(N-N) absorption at 2125 cm-1, which was replaced by two v(Co-H) absorptions at 1967 and 1833 cm-1. Treatment of the dihydrogen complexes with N2 afforded the starting material 4. [Pg.380]

The apparent half-hfe of reactivation can range from minutes to weeks, depending upon the enzyme, inhibitor, pH, and temperature. Reactivation can appear to be slow or nonexistent if aging has occurred, because the aged form of the phosphylated enzyme is stable to hydrolysis and will not reactivate (Jianmongkol et al, 1999 Richardson, 1992). [Pg.865]

The physico-mechanical properties of aminoplasts in the articles are determined by the degree of hardening and macrostructural defects. In the cooling of the articles down to room temperature reactive groups in the polymer are still retained, but their interaction is made difficult due to the loss of mobility caused by the molecules of the reticular polymer because of the latter s vitrification. Simultaneously a nonequilibrium supramolecular structure is recorded. Heat treatment of the articles does not alter the supramolecular structure, the latter remaining invariable. Heat treatment at a temperature below the vitrification temperature may only cause either a certain additional hardening of the binder or increase the... [Pg.60]

The issues related to containment of reaction components are sometimes underestimated in their importance. Their consequences, however, will surface quickly early in full implementation. Some general material characteristics have been discussed in Chapter 4, but they are mostly limited to the temperature and chemical environment typical of traditional separation applications. The material aspects of the membrane related to high-temperature reactive and permeating conditions will be reviewed in this section. [Pg.367]


See other pages where Temperature reactivity is mentioned: [Pg.445]    [Pg.385]    [Pg.261]    [Pg.302]    [Pg.371]    [Pg.206]    [Pg.822]    [Pg.634]    [Pg.302]    [Pg.371]    [Pg.466]    [Pg.257]    [Pg.615]    [Pg.950]    [Pg.300]    [Pg.15]    [Pg.175]    [Pg.231]    [Pg.1166]    [Pg.187]    [Pg.85]    [Pg.108]    [Pg.69]    [Pg.233]    [Pg.500]    [Pg.245]    [Pg.292]   
See also in sourсe #XX -- [ Pg.213 ]




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Autoignition temperatures, reactive

Autoignition temperatures, reactive chemicals

Coolant Temperature Coefficient of Reactivity

Effects of Temperature and Reaction Medium on Radical Reactivity

Graphite Temperature Coefficient of Reactivity

Heat-reactivation temperature

Inverse temperature-reactivity relationship

Negative temperature coefficient reactivity

Polymer high temperature, reactive oligomer

Reactive Melt Infiltration of Carbon Fiber Reinforced Ceramic Composites for Ultra-High Temperature Applications

Reactive at high temperature

Reactivity ratio temperature effects

Reactivity temperature coefficient

Temperature coefficient of reactivity

Temperature reactive distillation

Temperature reactivity relative

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