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Evaluation of catalytic activity

Now the principles and methods about applying flow method to determine the catal3dic activity have been proposed. Using these principles and methods can reduce the impact of macro-factors on activity measurement and the study on dynamics to a minimum. Here, in order to eliminate the wall effect of gases flow and local over-heating of beds, the ratio of diameter (dr) of reactor and particle size (dg) of catalyst should be 6 dr/dg 12. The wall effect can be neglected when dr/dg 12. However, as someone points out, even when dr/dg 30, the flow speed of the liquid close to the wall is 10% to 20% higher than that of the bed axis direction, which is obviously related to effect of reaction heat. [Pg.558]

On the other hand, reactions with a greater reaction heat have more difficulties in heat dissipation of bed when dr/dg 12, because the temperature differences between cross-section center and the radial of catalyst bed are decided by the following equation.  [Pg.558]

It can be seen from equation (7.15) that the temperature difference is proportional to reaction rate, heat effect and the square of diameter of the reactor, and is inversely proportional to the effective conductivity factor. The temperature difference increases with a decrease in the particle diameter of catalysts because the effective conductivity factor A reduces with the decrease in the size of catalyst particles. When decreasing the particle diameter of catalyst in order to eliminate the effect of inside diffusion on reaction, it also enhances the factor of temperature difference. Therefore, it need to weigh the pros and cons of these factors in order to determine the most appropriate particle size of catalyst and the diameter of reactor. [Pg.558]

If the inlet flow rate of (N2 + 3H2) without ammonia is Vq, the flow rate of formed anunonia is V, the residual gases after absorbed by sulfuric acid is V2K, according to mass balance for N2 + H2 gases in the system we get  [Pg.559]

The above equation obtains the space velocity based on the inlet gases of (3H2 + N2), also called space velocity without ammonia. Based on the volume (Vi) of gas (H2 + N2 + NH3) in reactor outlet, we calculate the space velocity S y), that is. [Pg.560]


Two space velocities, i.e. 0.03 and 0.3 h l, have been used in the evaluation of catalytic activities of catalysts B and C at 823 K. Figure 6 shows a decrease in activity of the catalyst B when space velocity increases. The accessible sites are saturated at the lowest space velocity. This explains thus the lower conversion levels at a higher space velocity. However, for catalyst C, the evolution of the conversion, which is also depicted in Figure 6, is almost identical for both space velocities. This result could be explained by a better dispersion of the platinum due to the presence of tin. [Pg.83]

Calculation of the Endocellulase Activity from the Intrinsic Viscosity Values. The enzymic degradation of polymeric substrates can occur at different bonds in the same substrate molecule, and the enzymic activity has to be defined here as the initial number of moles of glyco-sidic bonds split per second (53). This definition corresponds to the definition of the katal, symbolyzed kat. This unit is defined as the catalytic amount of any catalyst (including any enzyme) that catalyzes a reaction rate of one mole per second in an assay system (54), and it is recommended by the International Union of Pure and Applied Chemistry (55) for the quantitative evaluation of catalytic activities. [Pg.123]

Chen TL, Chen C, Bergeron NQ, Qose BE, Bohrer TJ, Vertel BM, Colley KJ. The two rat a2,6-sialyltransferase (ST6Gal I) isoforms evaluation of catalytic activity and intra-Golgi localization. Glycobiology 2003 13(2) 109-117. [Pg.646]

Nanostructured LaNiOs was prepared by co-precipitation under ultrasonic radiation [120], Using various characterization methods and evaluation of catalytic activity, the effects of ultrasound on the structural properties and catalytic activity of LaNiOs were studied. The TEM showed that the ultrasound could cause a decrease in the particle size. The average particle size of LaNiOs prepared by sonochemistry is 20 nm. The specific surface area of LaNiOs is 11.27 m g h Ultrasound could lead to increased surface oxide content and surface crystal oxygen vacancies. The TPR result showed that the LaNi03 prepared by sonochemistry has a lower reduction temperature and a higher ratio of surface oxygen to crystal oxygen. The evaluation of catalytic activity showed that ultrasound could increase the catalytic activity of LaNiOs for NO decomposition. [Pg.143]

Evaluation of catalytic activity in selective oxidation of styrene and benzene... [Pg.582]

EVALUATION OF CATALYTIC ACTIVITY Micro-reactor tests... [Pg.396]

The evaluation of catalytic activity for fresh catalyst A and catalyst A used for the 70 000 km test were also measured in Table 12. [Pg.402]

In Figure 1 the experimental apparatus used for the evaluation of catalytic activity is shown. [Pg.608]

We suggest the original method for evaluation of catalytic activity of complexes formed in situ at the beginning of reaction and in developed process, at elementary stages of oxidation process [33, 90-93] by simplified scheme assuming quadratic termination of chain and equality to zero of rate of homolytic decomposition of ROOH. In the If amework of radical-chain mechanism the chain termination rate in this case will be Eq. (1) ... [Pg.38]

In addition to the amperometric feedback mode described above, other amperometric operation modes are also possible. For example, in the substrate generation/tip collection (SG/TC) mode, ip is used to monitor the flux of electroactive species from the substrate and vice versa for the tip generation/substrate collection (TG/SC) mode. These operation modes will be described in Section 12.3.1.3 and are useful in studies of homogeneous reactions that occur in the tip-substrate gap (see Section 12.4.2) and also in the evaluation of catalytic activities of different materials for useful reactions, e.g., oxygen reduction and hydrogen oxidation (see Section 12.4.3). In addition to the amperometric methods, other techniques, e.g., potentiometric method is also applicable for SECM and will be discussed in Section 12.3.2. We will also update the techniques suitable for the preparation of SECM amperometric tips in Section 12.3.1.1 and potentiometric probes in Section 12.3.2.2. [Pg.473]

In order to investigate the catalytic activity of Ru catalysts, and compare with iron catalyst, we choose the representative iron catalyst A301 with wiistite as precursor as the reference sample. A301 has the highest activity among all of the iron-based catalysts for ammonia synthesis and now it has been widely used in ammonia synthesis industry. In order to get the reliable and comparable data of the evaluation of catalytic activity, the experiment was conducted under the same conditions and four samples were filled in four reactor contained in one shell. The results were shown in Table 6.41 and Figs. 6.56-6.58. [Pg.501]

Figure 7.10 (a) Evaluation of catalytic activity for soot oxidation of rice-ball Ag ... [Pg.386]

Until a few years ago, the TG/SC mode of SECM operation was the most common way to image an enzyme that catalyzes oxygen reduction. TG/SC mode is well suited for imaging activity of surfaces with morphological features because it is relatively insensitive to changes in the tip-substrate distance [14]. The main difference between this mode and classical FB mode is that the feedback diffusion process is not required for TG/SC mode, which enables a direct measurement of activity in acidic solutions. This mode is the converse of SG/TC mode used for the anode catalysts. TG/SC mode has been applied to the study of the kinetics of oxygen reduction reaction (ORR) [14], evaluation of catalytically active nonprecious metal alloy compositions [57,58], optimization of Cu(II) biomimetics [59], thermodynamics-based design of catalysts [60], and analysis of wired enzyme architectures [61]. [Pg.286]

Evaluation of catalytic activity Test reactiQns-Hvdtogqiation of Pvicne and 1- hexoie Reaction conditions-100 C. charge pressure- 100 nsig 22°C. [Pg.642]

Figure 6.64 Representative N-sulfinyl (thio)ureas evaluated for catalytic activity in the asymmetric aza-Henry reaction of N-Boc-protected benzaldimine with nitroethane affording model product 1. Figure 6.64 Representative N-sulfinyl (thio)ureas evaluated for catalytic activity in the asymmetric aza-Henry reaction of N-Boc-protected benzaldimine with nitroethane affording model product 1.
Several different test reactions have been suggested to evaluate the catalytic activity of an acid catalyst as a measure of the number and strength of the active sites. The ideal test reaction is experimentally easy, fast, reproducible, requires only a small amount of catalyst, has simple kinetics, and should show little deactivation. It should also not be diffusion limited and affected by the particle or crystal size. While no one reaction fits all these criteria perfectly, we and apparently others - find that hexane cracking comes closer to the ideal than most other reactions. [Pg.262]

Preleminary experiments have been performed to evaluate the catalytic activity of the MCM-48 supported VOx catalysts, with equal V-loading, to study the effect of the coupling reagent. Table 2 summarizes the catalytic activity and selectivity of the catalysts for the gas-phase oxidation of methanol, which was used as a model reaction. [Pg.322]

Many working groups have modeled the performance of diesel particulate traps during the past few decades. Concentrated parameter models (CSTR assumption) have been applied for the evaluation of formal kinetic models and model parameters. The formal kinetic parameters lump the heat and mass transfer effects with the reaction kinetics of the complicated reaction network of diesel soot combustion. Those models and model parameters were used for the characterization of the performance of different filter geometries and filter materials, as well as of the performance of a variety of catalytically active coatings and fuel additives [58],... [Pg.445]

Catalyst Screening. In order to determine the broad pattern of catalytic activity with respect to metal and oxide surface, a series of supported catalysts, prepared in a similar way, were evaluated. For these experiments the catalyst loading level is... [Pg.318]

Alkene hydrogenation, alkane hydrogenolysis, and methanation of CO are used as test reactions for evaluating the catalytic activity of cluster-derived metal catalysts. Catalysts derived from noble metal carbonyl precursors such... [Pg.331]

Use of apoenzymes for the detection of metal ions Generally, apoenzymes of metalloenzymes can be used for the detection of the corresponding metal ion. Restoration of enzyme activity obtained in the presence of the metal ion can be correlated to its concentration. This principle has been demonstrated in the detection of copper while evaluating reconstituted catalytic activities in galactose oxidase and ascorbate oxidase and also in the detection of zinc since this ion is essential for the activity of carbonic anhydrase and alkaline phosphatase [416]. The need of stripping the metal for the preparation of the apoenz5une may demand tedious procedures and a catalytic assay with the addition of the substrate is always required for detection. [Pg.137]

The cyclohexene conversion to paraffins and olefins which is well known as the Hydrogen Transfer Index (HTl) ratio was used to evaluate the catalytic activity of the fi sh and deactivated materials at constant conversion (30 mol %) varying the contact time and at 250°C. The HTl results were related with the REO content, cell parameter and total acidity and are plotted in figures 5,6 and 7, respectively. [Pg.396]

The development of emission spectrographic procedures and the choice of catalytically active proteins for purification have somewhat altered present evaluation and procedure. The simultaneous detection of all metals including zinc serves as a guide to contamination. The presence of extraneous ions and their decrease in concentration with increasing purity of the enzyme has become an index of the state of purity of the preparation, of the introduction of contaminants, and of the relationship of metals to enzyme action. [Pg.338]

Oxidation of toluene was employed to evaluate the catalytic activity and selectivity of the Mo-Ce complex oxides. The particle size, surface area and structure of ultrafine complex... [Pg.904]

The above scheme shows the importance of both adsorption and desorption processes. Adsorption of at least one of the reactant molecules is required for catalysis to occur. If the accelerated rate of reaction is simply due to the concentration of molecules at the surface, catalysis may result from physisorption of the reactants. On the other hand, chemisorption can be used primarily to quantitatively evaluate the number of surface active sites, which are likely to promote (catalyze) chemical reactions. Chemisorption analyses are applied to physically characterize a catalyst material, to determine a catalyst s relative efficiency in promoting a particular reaction, to study catalyst poisoning, and in monitoring the degradation of catalytic activity over time of use. [Pg.305]

Thus the objective of this study is to find the best combination of binder and zeolite composition for washcoating silicalite (a pentasil type zeolite) on a ceramic honeycomb substrate, and to evaluate the catalytic activity for methanol conversion. This will demonstrate the utility of zeolite honeycomb catalysts for chemical processing. [Pg.493]

Cfi Aromatic Reactions Without Hydrogen. In the present study, tire aluminophosphate molecular sieves have been used alone and with added platinum and hydrogen to isomerize Cs aromatic feeds. In an initial screening study, a series of large to medium pore size molecular sieves were evaluated for catalytic activity for m-xylene rearrangements at 1000° F without added metal and hydrogen. [Pg.522]


See other pages where Evaluation of catalytic activity is mentioned: [Pg.182]    [Pg.484]    [Pg.557]    [Pg.843]    [Pg.182]    [Pg.484]    [Pg.557]    [Pg.843]    [Pg.359]    [Pg.77]    [Pg.461]    [Pg.49]    [Pg.92]    [Pg.353]    [Pg.521]    [Pg.309]    [Pg.181]    [Pg.5282]    [Pg.652]    [Pg.128]    [Pg.185]    [Pg.489]    [Pg.33]    [Pg.185]   


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