Anisotropy is removed by setting the anisotropy ratio to 1 : 1 and adjusting the diffusion coefficient such that the overall activation time is comparable to control.
But the profound retardation of the drug release from the geopolymer structures opens up for precise control of the sustained release rates, simply by adjusting the size of the pellets and thereby affecting the diffusion length in the structures.
The diffusion-sensitivity can be varied by adjusting the "b-factor", which represents the gradient duration, gradient amplitude and the time interval between the two gradients.
The diffusion coefficient for AMPARs is adjusted by adjusting the viscosity of the membrane environment [ 30].
The critical growth area might be dependent on the surface diffusion, which could be improved by adjusting the grating parameters.
By adjusting the modulation frequency f one can vary the thermal diffusion length of the sample μ s and restrict the discussion to the case where Eq. (1) holds.
Control of the diffusion of sodium from SLG to CIGSe is possible by adjusting the Mo intergrain properties.
The lower uniformity in 0g case is owing to the initial gradient distribution of protein concentration in liquid/liquid diffusion crystallization, but it could be improved by adjusting the initial conditions of protein crystallization.
The kinetics was quantitatively analyzed and found to be diffusion rate controlled, allowing for precise tuning of particle size by adjusting the withdrawal speed.
