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添加91字节 、 2020年11月27日 (五) 16:54
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===Non-equilibrium state variables===
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=== Non-equilibrium state variables 非平衡状态变量 ===
    
The suitable relationship that defines non-equilibrium thermodynamic state variables is as follows. On occasions when the system happens to be in states that are sufficiently close to thermodynamic equilibrium, non-equilibrium state variables are such that they can be measured locally with sufficient accuracy by the same techniques as are used to measure thermodynamic state variables, or by corresponding time and space derivatives, including fluxes of matter and energy. In general, non-equilibrium thermodynamic systems are spatially and temporally non-uniform, but their non-uniformity still has a sufficient degree of smoothness to support the existence of suitable time and space derivatives of non-equilibrium state variables. Because of the spatial non-uniformity, non-equilibrium state variables that correspond to extensive thermodynamic state variables have to be defined as spatial densities of the corresponding extensive equilibrium state variables. On occasions when the system is sufficiently close to thermodynamic equilibrium, intensive non-equilibrium state variables, for example temperature and pressure, correspond closely with equilibrium state variables. It is necessary that measuring probes be small enough, and rapidly enough responding, to capture relevant non-uniformity. Further, the non-equilibrium state variables are required to be mathematically functionally related to one another in ways that suitably resemble corresponding relations between equilibrium thermodynamic state variables.<ref name="Gyarmati 1970"/> In reality, these requirements are very demanding, and it may be difficult or practically, or even theoretically, impossible to satisfy them. This is part of why non-equilibrium thermodynamics is a work in progress.
 
The suitable relationship that defines non-equilibrium thermodynamic state variables is as follows. On occasions when the system happens to be in states that are sufficiently close to thermodynamic equilibrium, non-equilibrium state variables are such that they can be measured locally with sufficient accuracy by the same techniques as are used to measure thermodynamic state variables, or by corresponding time and space derivatives, including fluxes of matter and energy. In general, non-equilibrium thermodynamic systems are spatially and temporally non-uniform, but their non-uniformity still has a sufficient degree of smoothness to support the existence of suitable time and space derivatives of non-equilibrium state variables. Because of the spatial non-uniformity, non-equilibrium state variables that correspond to extensive thermodynamic state variables have to be defined as spatial densities of the corresponding extensive equilibrium state variables. On occasions when the system is sufficiently close to thermodynamic equilibrium, intensive non-equilibrium state variables, for example temperature and pressure, correspond closely with equilibrium state variables. It is necessary that measuring probes be small enough, and rapidly enough responding, to capture relevant non-uniformity. Further, the non-equilibrium state variables are required to be mathematically functionally related to one another in ways that suitably resemble corresponding relations between equilibrium thermodynamic state variables.<ref name="Gyarmati 1970"/> In reality, these requirements are very demanding, and it may be difficult or practically, or even theoretically, impossible to satisfy them. This is part of why non-equilibrium thermodynamics is a work in progress.
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The suitable relationship that defines non-equilibrium thermodynamic state variables is as follows. On occasions when the system happens to be in states that are sufficiently close to thermodynamic equilibrium, non-equilibrium state variables are such that they can be measured locally with sufficient accuracy by the same techniques as are used to measure thermodynamic state variables, or by corresponding time and space derivatives, including fluxes of matter and energy. In general, non-equilibrium thermodynamic systems are spatially and temporally non-uniform, but their non-uniformity still has a sufficient degree of smoothness to support the existence of suitable time and space derivatives of non-equilibrium state variables. Because of the spatial non-uniformity, non-equilibrium state variables that correspond to extensive thermodynamic state variables have to be defined as spatial densities of the corresponding extensive equilibrium state variables. On occasions when the system is sufficiently close to thermodynamic equilibrium, intensive non-equilibrium state variables, for example temperature and pressure, correspond closely with equilibrium state variables. It is necessary that measuring probes be small enough, and rapidly enough responding, to capture relevant non-uniformity. Further, the non-equilibrium state variables are required to be mathematically functionally related to one another in ways that suitably resemble corresponding relations between equilibrium thermodynamic state variables. Onsager 1931, also), time rate of entropy production (Onsager 1931), dissipative structure, but they are hardly touched on in the present article.
 
The suitable relationship that defines non-equilibrium thermodynamic state variables is as follows. On occasions when the system happens to be in states that are sufficiently close to thermodynamic equilibrium, non-equilibrium state variables are such that they can be measured locally with sufficient accuracy by the same techniques as are used to measure thermodynamic state variables, or by corresponding time and space derivatives, including fluxes of matter and energy. In general, non-equilibrium thermodynamic systems are spatially and temporally non-uniform, but their non-uniformity still has a sufficient degree of smoothness to support the existence of suitable time and space derivatives of non-equilibrium state variables. Because of the spatial non-uniformity, non-equilibrium state variables that correspond to extensive thermodynamic state variables have to be defined as spatial densities of the corresponding extensive equilibrium state variables. On occasions when the system is sufficiently close to thermodynamic equilibrium, intensive non-equilibrium state variables, for example temperature and pressure, correspond closely with equilibrium state variables. It is necessary that measuring probes be small enough, and rapidly enough responding, to capture relevant non-uniformity. Further, the non-equilibrium state variables are required to be mathematically functionally related to one another in ways that suitably resemble corresponding relations between equilibrium thermodynamic state variables. Onsager 1931, also), time rate of entropy production (Onsager 1931), dissipative structure, but they are hardly touched on in the present article.
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定义非平衡热力学状态变量的合适关系如下。当系统碰巧处于足够接近热力学平衡的状态时,非平衡态变量可以通过与测量热力学状态变量相同的技术,或者通过相应的时间和空间导数,包括物质和能量的流动,足够精确地在局部测量。一般来说,非平衡态热力学系统在空间和时间上都是不均匀的,但是它们的不均匀性仍然具有足够的光滑度来支持存在合适的非平衡态变量的时间和空间导数。由于空间非均匀性,对应于广义热力学状态变量的非平衡状态变量必须定义为相应广义平衡状态变量的空间密度。在系统足够接近热力学平衡的情况下,密集的非平衡状态变量,例如温度和压力,与平衡状态变量密切对应。为了获得相应的非均匀性,测量探头必须足够小,响应速度也必须足够快。此外,非平衡状态变量需要在数学上相互之间以适当类似于平衡热力学状态变量之间对应关系的方式进行功能联系。昂萨格1931)、产生熵时间速率(昂萨格1931)、耗散结构,但在本文中几乎没有涉及。
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定义非平衡热力学状态变量的关系如下:在系统恰好处于很接近热力学平衡状态的情况下,非平衡状态变量可以通过与测量热力学状态变量相同的技术,或通过相应的时空导数,包括物质和能量通量,以足够的精度在本地进行测量。通常,非平衡热力学系统在空间和时间上都是非均匀的,但是它们的非均匀性仍然具有足够的平滑度,以保证非平衡状态变量的时空导数适当存在。另外由于空间的不均匀性,必须将非平衡状态变量(对应于广义热力学状态变量)定义为相应的广义平衡状态变量的空间密度。在系统足够接近热力学平衡的情况下,密集的非平衡状态变量(例如温度和压力)与平衡状态变量紧密对应。测量时探头必须足够小,并且响应速度要足够快,以捕获相关的不均匀性。此外,要求非平衡状态变量在数学上彼此函数相关,其方式应类似于平衡热力学状态变量之间的对应关系。实际上,这些要求非常苛刻,可能很难实现,或实际上,甚至在理论上无法满足它们。这就是非平衡热力学的研究一直处在探索中的部分原因。
    
==Overview==
 
==Overview==
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