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Mn reaction

Fig. 3.2 XRD spectra showing the process of PbSe formation from the reaction of precipitated hydrated lead oxide with Na2SeS03 solution, (a) Starting material (b-e) after 1.5, 3, 4.5, and 6 mn reaction, respectively. (Adapted from Ref. 46.)... [Pg.119]

Balance oxygen atoms. There are no oxygen atoms in the Fe halfreaction. There are four oxygen atoms on the left side of the Mn reaction, so we add four molecules of H20 to the right side ... [Pg.711]

Fig. 5.4. The chemical route for the synthesis of RuxSey. The initial chemical precursors dissolved in xylene (a) Ru3(CO)i2 and (b) elemental selenium (b). 13C NMR spectmm of a solution after 40 mn reaction time. The chemical shifts 199.67 ppm belongs to (a) and 198.89 ppm to (c) Ru4Se2(CO)n. The non-stoichiometric reaction (below) describe schematically the complex chemical interplay leading to cluster-like compound RuxSey. Fig. 5.4. The chemical route for the synthesis of RuxSey. The initial chemical precursors dissolved in xylene (a) Ru3(CO)i2 and (b) elemental selenium (b). 13C NMR spectmm of a solution after 40 mn reaction time. The chemical shifts 199.67 ppm belongs to (a) and 198.89 ppm to (c) Ru4Se2(CO)n. The non-stoichiometric reaction (below) describe schematically the complex chemical interplay leading to cluster-like compound RuxSey.
With the soluble catalysts, yields above 80% are obtained after 10 mn and 90% after 30 mn reaction time. These biguanides are about thirty times more reactive than soluble guanidines 60% yield after 5 mn instead of the 180 mn. [Pg.142]

The polystryrene-bound biguanides were checked under exactly the same conditions and exhibited excellent catalytic properties (Table 1). The immobilization of the biguanide units induced only a very limited decrease in the reactivity. Yields above 90% were obtained in less than 15 mn. The yields of methyl esters are above 94% even before 15 mn reaction time. [Pg.142]

These biguanide-supported catalysts are far more reactive and more stable than the previously described guanidines.,7b This confirms the higher basicity of biguanides vs. guanidines and that their immobilisation induces only a very limited decrease in reactivity 90% instead of 94% yield after 30 mn reaction time. [Pg.142]

Using the Mn02—Mn " reaction as an example, equation 7.5, written in terms of pe, provides the pc-pH relationship ... [Pg.254]

If the Mn activity in soil solution were more or less constant (perhaps controlled by ion exchange processes), then pc and pH would, as observed, be negatively correlated. Closer scrutiny of the pc-pH relationship in soils, however, reveals that the slope of the function tends to be near 1. This would be predicted if the controlling redox reaction(s) in the soil involved equal numbers of protons and electrons (that is, m = in reaction 7.1). This is clearly not the case for the Mn02—Mn reaction, whose pc-pH function has a slope of 2. For the O2—H2O and several other important redox couples in soils, however, the expected slope is at or near unity (Table 7,1 lists redox couples along with the number of protons and electrons consumed by reduction). [Pg.254]

Variable Catalyst Concentration Solutions. Using the mass transfer coefficient of 0.015 cm/sec, the model was then used to simulate the slurry oxidation with three concentrations of added Mn catalyst. Results are presented in Figure 8. The 1.5 order homogeneous reaction rate constants for 0, 6.66, and 200 ppm added Mn reactions were found from the model to be 0.35, 2.25, and 5.5 2,0 5 mol-0 5 sec-1 respectively. The corresponding values of 1.5 order rate constants from the comparable clear solution experiments are 0.162, 0.35, and 0.8 to 5... [Pg.212]

The oxides of manganese also catalyze the oxidation of Mn to Mn Zapffe (256) found that the oxidation of manganese in a water treatment plant was speeded up, following aeration, by the catalytic infiuence of pyrolusite ()8-Mn02) and also by in situ precipitated manganese oxide. Hem (94) noted a catalytic effect of feldspar on the Mn to Mn reaction rate. It seems likely that this was caused by minute amounts of manganese oxide impurities on the feldspar surfaces. [Pg.355]

In addition, the possibility to mn reactions automatically in a continuous or repetitive manner would also be regarded as an advantage. [Pg.137]

Fig. 14.3 For the general reaction, M + N MN, reaction can only occur if molecules M and N collide. The chance of collisions between M and N molecules falls as more product (MN) molecules are made. Fig. 14.3 For the general reaction, M + N MN, reaction can only occur if molecules M and N collide. The chance of collisions between M and N molecules falls as more product (MN) molecules are made.
Theorell-Chance mechanism is a simplified version of an Ordered Bi Bi mechanism where the steady-state level of central complexes is very low. TheoieU and Chance (1951) have proposed an Ordered Bi Bi mechanism without the central ternary complexes for alcohol dehydrogenase from equine liver. The hit-and-mn reaction sequence can be written ... [Pg.155]

Portehault D, Cassaignon S, Emmanuel B, Joliver IP. Structural and morphological control of manganese oxide nanoparticles upon soft aqueous precipitation through MnO. /Mn " " reaction. J Mater Chem 2009 19 2407-16. [Pg.528]

Jiang X, Chen Z, Huang S, Wang J, Pan Y (2014) A red phosphor BaTiF6 Mn reaction mechanism, microstructures, optical properties, and applications for white LEDs. Dalton Trans 43 9414... [Pg.397]

MnHMA MnS+ Cyclic voltammetry Mn + electrochemically active showing Mn +/Mn + reaction (238)... [Pg.1634]

Frequently the nuclear reaction Ni (n,p) Co is used for determination of the fast neutron fluence, but it has two severe drawbacks when compared to the Fe-Mn reaction described above The rather short halflife of Co of 71.3 days limits the application of this reaction to irradiation times of less than 150 days, even when the irradiation history of the sample is taken into account. In addition, the complex nature of the nuclear reaction requires expensive calculations when accurate results are required. On the other hand, the intense y ray of Co at 0.81 MeV (transition probability 99.5%) can be easily measured using a Ge detector, in most cases making chemical separation work unnecessary. [Pg.155]

The effective threshold energy of the reaction is about 3 MeV, which means it is very similar to that of the Fe (n,p) Mn reaction. The total cross section values... [Pg.155]

Further, the crystal phase or morphology within the electrode structure is irreversibly lost. An example of this situation is seen for dissolution of Mn02 in its Mn + and Mn states [30,29]. The Mn + Mn + redox occurs at 0.47 V versus NHE, while the Mn +<->Mn + reaction occurs at 1.19 V versus NHE under neutral pH ( 6.5). In a symmetric design, this restricts the potential window... [Pg.119]

Characteristics of the industrial reactor 16 bipolar electrodes, total surface of 18.3 m. Current 4000 A flow about 7001/h Mn reaction mass at 80-85 °C. Yield about 90% Mn [140]. Four technical cells are in operation [140b] with an output of 100 t/year. [Pg.158]

Although the rate of hydrolysis of urea is larger than that of the removal of Mn, reaction (1) is the rate-determining step for the overall precipitation process. The selectivity of the utilization of the generated ammonium hydroxide is determined by equilibria (2) and (3). It is expected that hi er temperatures and/or a higher pH will favour (2) over (3). This Indeed explains that for experiment U33 the rate constant is lower than in the other cases, seeing that, as is shown in Fig. 2, the pH at which precipitation takes place is much higher. [Pg.28]


See other pages where Mn reaction is mentioned: [Pg.104]    [Pg.249]    [Pg.82]    [Pg.286]    [Pg.292]    [Pg.270]    [Pg.356]    [Pg.55]    [Pg.194]    [Pg.1202]    [Pg.64]    [Pg.20]    [Pg.88]    [Pg.463]    [Pg.22]   


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Mn-catalyzed reaction

Scheme 35. Reaction of le with 2-phenylethanol using Mn(CO)5Br as catalyst

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