热破坏理论中高分子纤维强度的暂时依赖性

E. Kartashov
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引用次数: 3

摘要

目标。本文用数学方法描述了高分子材料破坏过程中微观阶段和宏观阶段的相互影响,确定了其主要参数和极限特性。此外,还建立了表征材料结构的分子常数与表征其宏观强度特征的分子常数之间的关系。最后,从动力学热波动概念的角度,提出了聚合物纤维热破坏过程的热动力学理论表述,使预测热载荷下样品的热耐久性成为可能。采用结构动力学热波动理论描述了断裂过程的初始阶段,并推导了裂纹扩展速率的广义公式。裂纹的数学理论用于描述材料在试样的机械和热载荷作用下,在内部圆形裂纹附近的热应力状态。给出了从安全到临界机械应力范围内的耐久性全等温线的理论公式,以及聚合物纤维在纯热载荷下从安全到临界热载荷全范围和非热裂纹扩展阶段的强度随时间变化的理论关系式。指出了热载荷下耐久性的主要参数和极限特征。提出了纯热作用下聚合物纤维断裂的广义结构动力学理论。该理论结合了三种独立的方法:结构动力学(热波动理论)、力学和热力学。所得的理论关系对裂纹扩展动力学的局部化、强化和控制方法的发展具有实际意义。
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Thermal destruction of polymeric fibers in the theory of temporary dependence of strength
Objectives. This study mathematically describes the mutual influence of micro- and macrostages of the process of destruction of polymer materials and determines its main parameters and limiting characteristics. In addition, a relationship is established between molecular constants characterizing the structure of a material and those characterizing its macroscopic characteristics of strength. Finally, theoretical representations of the thermokinetics of the process of thermal destruction of polymer fibers from the standpoint of the kinetic thermofluctuation concept are developed, which makes it possible to predict the thermal durability of a sample under thermal loading.Methods. The structural–kinetic thermofluctuation theory was used to describe the initial stages of the fracture process and to derive a generalized formula for the rate of crack growth. The mathematical theory of cracks is used to describe the thermally stressed state of a material in the vicinity of an internal circular crack under mechanical and thermal loadings of the sample.Results. A theoretical formula for the full isotherm of durability in the range of mechanical stresses from safe to critical, as well as a theoretical relationship for the time dependence of the strength of polymer fibers under purely thermal loading in the full range of heat loads from safe to critical and at the stage of nonthermal crack growth, is given. The main parameters and limiting characteristics of durability under thermal loading are also indicated.Conclusions. A generalized structural–kinetic theory of the fracture of polymer fibers under purely thermal action on cracked specimens is presented. The developed theory combines three independent approaches: structural–kinetic (thermofluctuation theory), mechanical, and thermodynamic. The obtained theoretical relations are of practical interest for the development of methods for localization, intensification, and control of the crack growth kinetics.
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