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Dynamical destabilization of system characterized by activation/inhibition kinetics using a differential flow

机译:系统的动态不稳定,其特征在于使用微分流的激活/抑制动力学

摘要

A new method of inducing spatiotemporal structures in systems characterized by activation/inhibition kinetics through the action of a differential bulk flow of the key species is disclosed. As Turing predicted, a homogeneous and otherwise stable steady state of a reactive system may lose its stability and form inhomogeneous patterns due to the interaction of diffusion and reaction. This mechanism is believed to form the basis of biological morphogenesis. The Turing instability only arises in systems wherein the diffusion coefficient of the inhibitor is sufficiently greater than that of the activator. The method of the present invention avoids this constraint by using a differential flow between the activation and the inhibition species rather than a differential diffusivity. In one aspect of the invention, this differential flow is achieved by immobilizing one of either the inhibitor or activator species in the flow system containing the other species. The resulting destabilized system, which in this aspect is a BZ reaction, is characterized by travelling waves whose length and propagation velocity are proportional to the flow rate. Technological advantages are disclosed that arise from the operation of a kinetic system under such conditions of differential flow that give rise to the dynamical instability.
机译:公开了一种通过关键物质的不同总体流量的作用在以活化/抑制动力学为特征的系统中诱导时空结构的新方法。正如图灵所预测的那样,由于扩散和反应的相互作用,反应体系的均质和稳定状态可能会失去其稳定性并形成不均匀的模式。据信该机制形成生物学形态发生的基础。图灵不稳定性仅在抑制剂的扩散系数比活化剂的扩散系数足够大的系统中出现。本发明的方法通过使用活化和抑制物质之间的差流而不是差扩散率来避免这种约束。在本发明的一方面,通过将抑制剂或活化剂物质之一固定在含有另一种物质的流动系统中来实现这种差异流动。最终的不稳定系统,在这个方面是BZ反应,其特征在于行波的长度和传播速度与流速成正比。公开了在动力学系统的操作中产生的技术优势,这种动力学系统在这种差动流动的条件下引起动力学的不稳定性。

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