-The relation between the structure and meckmnlcal fracture of oriented polymers is discussed. The fracture behaviour originates from the structural heterogeneity of polymers, i . e . , the presence of nicro-and macrofibrils, alternating crystalline and disordered (amorphous) regions along microfibrils etc. The fracture behaviour of polymers is analyzed in terms of the kinetic thermal-fluctuation concept O f strength of solids. The phonon mechanism of nucleation of the breaking thermal fluctuations in disordered regions of microfibrils is discussed. A Critical role played by kink band formation in the appearance of localized submicro-and microcracks is elucidated. The mechanism of propagation of the main crack is revealed through studies of the electron microscopic fractograms from the rupture surfaces of fibers. The need for an analysis of the polymer fracture in terms of the nonequilibrium system' theory is emphasized.The study of basic laws governing mechanical fracture Of oriented polymers is extremely important both for scientific researoh and practical applications. Since high-strength, highly oriented cord fibers, monofilaments, oriented films are now produced industrially at the rate of many millions of tons per year, a further Improvement of the mechanical performance of these materials is a burnin problem. garded as relatively well-defined one-dimensional systems which represent a suitable model object for studying the fracture behaviour at the molecular and supermolecular levels of polymer architecture.There are several currently available techniques for preparation of oriented polyners. They include orientation drawi y , high pressure extrusion, crystallization from dilute solu ions under shear etc. (Refs. 1-3). mers obtained by these techniques can differ appreciably (Refs. 1-31, which is sure to affect their behaviour during mechanical fracture.The most widely used method of mass production of oriented polymers is an orientation drawin from the solid unoriented state. The structure of the oriented polymers thus obtained has proven a matter of considerable controvers (Befs.1,3,4). Analysis of the available data reveals (Ref. 4y the existence of two levels of heterogeneity in the supermolecular organization, i.e., macrofibrils and microfibrils. the polymer bulk distinquishable by electron microscopy and X-ray diffraction. These are fiber-like formations several On the other hand, highly orienfed polymers can be reIt is worth noting that the structure of oriented polyMicrofibrils (Rlg.1) are minor supermolecular elements in