Drawback of the constant K type filter is that at the cut of frequency , its attenuation is a steady curve .. quick response is lacking in it
an ideal filter should have a sharp response curve.
The units of the equilibrium constant K in a chemical reaction are dimensionless.
The rate constant k in a chemical reaction can be determined by conducting experiments to measure the reaction rate at different concentrations of reactants. By plotting the data and using the rate equation, the rate constant k can be calculated.
The rate constant k is dependent on factors such as temperature, concentration of reactants, presence of catalysts, and the nature of the reaction mechanism.
To determine the equilibrium constant from the change in Gibbs free energy (G), you can use the equation G -RT ln(K), where G is the change in Gibbs free energy, R is the gas constant, T is the temperature in Kelvin, ln is the natural logarithm, and K is the equilibrium constant. By rearranging this equation, you can solve for K to find the equilibrium constant.
To calculate the equilibrium constant from the change in Gibbs free energy (G), you can use the equation: G -RT ln(K), where G is the change in Gibbs free energy, R is the gas constant, T is the temperature in Kelvin, ln is the natural logarithm, and K is the equilibrium constant. By rearranging this equation, you can solve for K as K e(-G/RT).
in m derived impedance matching is possible but not in case of constant k filters. compared to constant k filter m derived filter has a sharp cutoff frequency. in k type the attenuation is not complete in the stop band.where as in the m derived just beyond the attenuation rises to max just after the cut off frequency. in m derived a capacitor and a inductor are taken in series at the output.
Eddie Randolph Fowler has written: 'Constant-k complementary filters'
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Boltzman constant
A formula involving a constant K typically represents a relationship where K is a fixed value, such as a proportionality constant or a parameter in an equation. The formula may use K to scale or modify the output based on the specific context or condition in which it is applied.
First order rate constant k is described in V=k[EA] while second order rate constant is given as V=k[E][A]. For reactions that do not have true order, k is the apparent rate constant.
limx→∞(k)=k, the limit of a constant k is equal to the constant k. Therefore, the limx→∞(6)=6.
The equation is xy = k where k is the constant of variation. It can also be expressed y = k over x where k is the constant of variation.
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Various options: y is directly proportional to k, with x as the constant of proportionality; y is directly proportional to x, with k as the constant of proportionality; x is inversely proportional to k, with y as the constant of proportionality; x is directly proportional to y, with 1/k as the constant of proportionality; k is directly proportional to y, with 1/x as the constant of proportionality; and k is inversely proportional to x, with y as the constant of proportionality.
Probably because constant starts with "k" in certain languages (like in German).