Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

High-temperature water, reaction analysis

The low temperature water-gas shift reaction is well described by a micro-kinetic model [C.V. Ovesen, B.S. Clausen, B.S. Hammershoj, G. Sreffensen, T. Askgaard, I. Chorkendorffi J.K. Norskov, P.B. Rasmussen, P. Stoltze and P.J. Taylor,/. Catal. 158 (1996) 170] and follows to a large extent the scheme in Eqs. (23-31). The analysis revealed that formate may actually be present in nonvanishing amounts at high pressure (Fig. 8.18). [Pg.326]

The uses of micelles in chemical analysis are rapidly increasing (Hinze, 1979). Analytical reactions are carried out typically on a small scale and are based on spectrophotometry. At the same time, undesired side reactions can cause major problems, especially when the analytical procedure depends on reactions which are relatively slow and require high temperatures, exotic solvents or high reagent concentrations for completion. Micelles can suppress undesired reactions as well as speed desired ones and they also solubilize reagents which are sparingly soluble in water. In addition it is often possible to make phosphorescence measurements at room temperature in the presence of surfactants which enormously increases the utility of this very sensitive method of detection. [Pg.281]

Combustion of transition metal organometallic compounds produces a mixtures of simple compounds (metal oxides, carbon oxides, water, nitrogen) which is subject to exact analysis. Thermal decomposition or high temperature iodination of the same compounds cannot necessarily be expected to produce simple materials, with the result that identification is often a difficult problem. This is typified by diene derivatives of iron carbonyl10, where side reactions of the dienes (e.g. polymerization) follow disruption of the iron-diene bonds. The oligomeric mixture can be parti-... [Pg.77]

Most hterature references to pharmaceutical primary process monitoring are for batch processes, where a model of the process is built from calibration experiments [110, 111]. Many of these examples have led to greater understanding of the process monitored and can therefore be a precursor to design of a continuous process. For example, the acid-catalysed esterification of butan-l-ol by acetic acid was monitored through a factorial designed series of experiments in order to establish reaction kinetics, rate constants, end points, yields, equilibrium constants and the influence of initial water. Statistical analysis demonstrated that high temperatures and an excess of acetic acid were the optimal conditions [112]. [Pg.257]

The thermodynamic analysis of loannides [193] on SRE in a solid polymer fuel cell indicated that the ethanol steam reforming reaction needs to be carried out in two steps a high-temperature endothermic step (steam reforming), in which ethanol is converted to a gaseous mixtures of H2, CO, CO2, CH4 and unreacted H2O, and a subsequent, low-temperature step (WGSR) in which CO reacts with water to form H2 and CO2. [Pg.199]

In 2008, Xiuyang et al. made an in-depth experimental study on the glucose decomposition in High Temperature Liquid Water (HTLW) from 180 to 220°C [73]. Interestingly, at 220°C, 100% of glucose was consumed within 90 min without addition of any catalyst. Analysis of the crude revealed that the main products of the reaction were HMF, levulinic acid, humic matter, and two unidentified soluble compounds. The maximum yield of HMF was obtained after 30 min of reaction (32%). [Pg.76]

If the rate sensitivity analysis is carried out over a non-isothermal oscillatory trace, then it is possible to see how certain reactions, in particular radical termination reactions and the reactions of water, become important at high temperatures and high conversions. The highest number of reactions is selected at the peak maximum where the temperature rises above 2000 K. All reactions required by the non-isothermal analysis, reactions 2-10, 13, 14, 16, 22-29, 35 and 45, were featured in one of the isothermal mechanisms. Therefore, it is possible to produce a reduced scheme for a non-isothermal simulation from an isothermal analysis provided the full... [Pg.337]


See other pages where High-temperature water, reaction analysis is mentioned: [Pg.78]    [Pg.190]    [Pg.100]    [Pg.1901]    [Pg.89]    [Pg.187]    [Pg.116]    [Pg.126]    [Pg.77]    [Pg.54]    [Pg.131]    [Pg.255]    [Pg.6]    [Pg.54]    [Pg.12]    [Pg.35]    [Pg.84]    [Pg.14]    [Pg.401]    [Pg.97]    [Pg.126]    [Pg.388]    [Pg.212]    [Pg.317]    [Pg.1901]    [Pg.67]    [Pg.139]    [Pg.194]    [Pg.125]    [Pg.39]    [Pg.183]    [Pg.309]    [Pg.88]    [Pg.282]    [Pg.273]    [Pg.498]    [Pg.203]    [Pg.260]    [Pg.332]    [Pg.505]    [Pg.103]    [Pg.11]   


SEARCH



Analysis temperature

High reactions

High water

High-temperature reaction

Water analysis

Water temperatures

© 2024 chempedia.info