Carbon-fiber composites have been made under laboratory conditions on the basis of partially crystallized polyimide (PI) matrices of R-ODFO type as modified by carbon nanofibers of VGCF type. The R-ODFO matrix is modified by nanofibers in an amount of 3 mass %, which leads to the following: firstly, an approximately tenfold reduction in the time for the crystallization of the PI matrix, and secondly, the viscosity of interlayer failure in the carbon plastic (for fibers Elur-0.08P) on the basis of the R-ODFO/VGCF composite is maintained at the fairly high level of about 1100 J/m 2 even with a high degree of crystallinity (about 40%) in the PI matrix, which cannot be done for the unmodified R-ODFO matrix. Triple composite can be made from a PI matrix, carbon microfibers of Elur type (volume content about 55%) and VGCF nanofibers (weight content in PI matrix about 3%), which provides a heat-resisting carbon plastic with a fairly high viscosity for interlayer failure.Polyimides (PI) are amongst the most effective polymers for electronics and aerospace research because of their good thermal and mechanical characteristics, as well as their radiation and chemical stability [1]. Particular interest attaches to PI capable of crystallizing from a melt, since additional advantages come from the crystalline structure such as elevated thermal stability and resistance to water and alkalis [2][3][4]. They are very promising as binders for fibrous composites, in particular carbon plastics (CP).For some years [5-10] we have been researching thermoplastic PI based on 1,3-bis-(3,3′,4,4′-dicarboxyphenoxy)benzene (R) and 4,4′-bis-(4-aminophenoxy)disphenyl (ODFO) for use as binders for carbon plastics:These R-ODFO binders have advantages over other partially crystalline PI [2][3][4] in the low melting point of T mp ≈ 320°C (vitrification temperature T v ≈ 204°C). The melt has the comparatively low viscosity η ≈ 10 3 Pa.sec at 340°C, which allows one to work such PI into composite matrices at temperatures reasonably far from the temperature at which thermal destruction of R-ODFO starts (about 450°C).The crystallization of the R-ODFO matrix after melting can be accelerated by modifying it with bis-imides of chemical structure similar to that of the PI itself, which is explained by the plastification effect, which increases the molecular mobility of the PI and correspondingly the capacity to crystallize [5][6][7].Macromolecular Compounds Institute, Russian Academy of Sciences.