The basic stages of the evolution of the technology for ceramic and refractory materials are directly related to refinement of the temporary industrial binders (TIB) used. This constituent of the molding mass and semifinished product determines the properties of the finished product to a significant degree. The information on TIB formulations is primarily concentrated in the patent literature. The number of studies and reviews of the main problems in making up molding masses, the reaction of the TIB with the ceramic solid phase, and planning of the industrial binder with consideration of the requirements for the finished products is limited [1-3]. This is partially due to the lack of unambiguous criteria for evaluating the quality of the masses and selecting binders and the complexities of using the experimental apparatus for methods of physical and colloid chemistry, mechanisms of disperse systems, and the physical chemistry of polymers. This is because dilute solutions, and not the concentrated solutions typical of ceramics technology, solutions of macromolecular compounds (MMC), and highly disperse fillers are the traditional objects. Due to the necessity of molding semiproducts of complex shape with elevated requirements for surface quality, geometric dimensions, and homogeneity, the urgency of developing new binder compositions has now increased significantly. The analysis of the assortment and trends in the development of TIB formulations can also be useful to some degree in creating new technological solutions. The requirement of increasing the level of the electrophysical properties of sparkplugs for internal combustion aircraft engines has led to the exclusion of clay plastic components from the composition of steatite masses and made it necessary to add molding powder to the composition to give the solution of polyvinyl alcohol (PVA) the required technological properties. The first publications on this problem date back to the mid-1940s [4, 5]. The tendency to reduce or eliminate some of the plastic components in the formulations for ceramic and refractory masses and to use temporary binders in ceramics technology has been tracked since the end of the 1930s. In the 1940sbeginning of the 1950s, a wide range of TIB based on aqueous solutions of natural and partially artificial macromolecular substances and products were used in production: flour, starch, gelatin, cellulose derivatives, alginates, and resins [6-8]. Generalization of the studies published in this period led to the formulation of principles for classification of TIB for molding of semiproducts of the basic kinds of industrial ceramics based on the origin and chemical nature of the polymer [9, 10]. Hypotheses were advanced in the same period concerning the complex physicochemical reactions in the ceramic material-MMC solution system [8], and the role of the viscosity of the dispersion medium in molding was emphasized [11]. Two limiting cases of the reaction in the ceramic material-TIB system and formation of the molding mass were formulated in 1961 [12]: due to the high viscosity of the dispersion medium (resin, petrolatum, etc.) in the almost total absence of any reaction between disperse phase and dispersion medium; with a strong reaction between TIB and solid phase and formation of cross-linked layers on the phase boundary with properties different from the properties of the dispersion medium in bulk. For the first time, a hypothesis was thus advanced concerning the possibility of formation of a plastic molding mass due to forming of interfacial boundary structures with anomalous properties. In the same period, an analogy was drawn in [13] for the structure of plastic hydrate-gel shells in clay masses and the boundary layers in dispersions of the oxide material- MMC