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Titration Total decomposition temperatures

Further acid site strength and concentration measurements were reported by Morita et al. (164), who related the acidity measurements to various catalytic reactions. Using Y zeolite (Linde SK-40, 90% H form) activated at 450°C, they observed no acid sites stronger than an H0 of -8.2, although the total acid site concentration was almost twice that of the former investigations (Fig. 21, curve 4). They also measured acid site concentration as a function of decomposition temperature for NH4Y, and found that n-butylamine titration values paralleled results obtained from pyridine adsorption studies (41,151). The maximum total acidity occurred... [Pg.145]

Thermogravimetry (TG) is a measure of the thermally induced weight loss of a material as a function of the applied temperature [39], Thermogravimetric analysis is restricted to studies involving either a mass gain or loss, and it is most commonly used to study desolvation processes and compound decomposition. Thermogravimetric analysis is a very useful method for the quantitative determination of the total volatile content of a solid, and it can be used as an adjunct to Karl Fischer titrations for the determination of moisture. [Pg.243]

The effect of temperature on ammonia adsorption by ZSM5 samples has been investigated by microcalorimetry, varying the adsorption temperature from 150 to 400°C [235]. The initial heats of adsorption were independent of temperature up to 300°C. When the adsorption temperature increased, there was a competition between the formation of ammonium ions on Brpnsted sites and their decomposition. The total number of titrated sites decreased with increasing adsorption temperature. It appeared that an adsorption temperature between 150 and 300°C is appropriate for these calorimetric experiments. [Pg.244]

Kinetic Studies. Peracetic Ac id Decomposition. Studies with manganese catalyst were conducted by the capacity-flow method described by Caldin (9). The reactor consisted of a glass tube (5 inches long X 2 inches o.d.), a small centrifugal pump (for stirring by circulation), and a coil for temperature control (usually 1°C.) total liquid volume was 550 ml. Standardized peracetic acid solutions in acetic acid (0.1-0.4M) and catalyst solutions also in acetic acid were metered into the reactor with separate positive displacement pumps. Samples were quenched with aqueous potassium iodide. The liberated iodine was titrated with thiosulfate. Peracetic acid decomposition rates were calculated from the feed rate and the difference between peracetic acid concentration in the feed and exit streams. [Pg.365]

Figure 1. (A) Effect of the titration temperature during Fe-decomplexation exchanged on the N2O decomposition activity using citrate Fe-precursor at ( ) 333 ( ) 353 and (A) 373 K. For comparison, a reference catalyst based on ion-exchange using ferric nitrate (same Fe loading) is included (O). Reaction conditions 4.5 mbar N2O, He balance. (B) Stability test for ( ) in A spot under typical conditions for nitric acid plants in The Netherlands 4.5 mbar N2O + 0.6 mbar NO + 15 mbar H2O + 75 mbar O2. In both cases, total pressure was 3 bar-a and a space time W/F (N20) of 900 kgxsxmoT (W is the catalyst mass and F (N20) the molar flow of N2O in the reactor inlet) was applied. Figure 1. (A) Effect of the titration temperature during Fe-decomplexation exchanged on the N2O decomposition activity using citrate Fe-precursor at ( ) 333 ( ) 353 and (A) 373 K. For comparison, a reference catalyst based on ion-exchange using ferric nitrate (same Fe loading) is included (O). Reaction conditions 4.5 mbar N2O, He balance. (B) Stability test for ( ) in A spot under typical conditions for nitric acid plants in The Netherlands 4.5 mbar N2O + 0.6 mbar NO + 15 mbar H2O + 75 mbar O2. In both cases, total pressure was 3 bar-a and a space time W/F (N20) of 900 kgxsxmoT (W is the catalyst mass and F (N20) the molar flow of N2O in the reactor inlet) was applied.

See other pages where Titration Total decomposition temperatures is mentioned: [Pg.101]    [Pg.35]    [Pg.66]    [Pg.270]    [Pg.185]    [Pg.499]    [Pg.59]    [Pg.555]    [Pg.332]    [Pg.19]    [Pg.46]    [Pg.122]    [Pg.123]   


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