We propose a theory of the dynamics of polymers in dilute solution, in which the popular Zimm and Rouse models are just the limiting cases of an infinitely large and small draining parameter. The equation of motion for the polymer segments (beads) is solved together with Brinkman's equation for the solvent velocity that takes into account the presence of other polymer coils in the solution. The equation for the polymer normal modes is obtained and the relevant time correlation functions are found. A tendency to the time-dependent hydrodynamic screening is demonstrated on the diffusion of the polymers as well as on the relaxation of their internal modes. With the growing concentration of the coils in the solution, they both show a transition to the exactly Rouse behaviour. The shear viscosity of the solution, the Huggins coefficient and other quantities are calculated and shown to be notably different from the known results.

The possibility of PO(4)(3-) for MoO(4)(2-) partial substitution in the langbeinite framework has been studied by exploration of the K-Fe(Sc)-Mo(W)-P-O systems using the high-temperature solution method. It was shown that 1/3PO(4)(3-) for MoO(4)(2-) substitution leads to formation of three novel compounds K(2)Fe(MoO(4))(PO(4))(2), K(2)Sc(MoO(4))(PO(4))(2), and K(2)Sc(WO(4))(PO(4))(2) with slightly increased lattice parameters and significant distortion of the anion tetrahedra without structure changes. In contrast, the antiferromagnetic structure is modified by substitution in the low-temperature region. The structural peculiarities are discussed in light of bond-valence sums calculations.

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