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化学 1873

论气态与液态的连续性

约翰内斯·迪德里克·范德瓦耳斯

气与液并非两种物质,而是同一种,由一道方程连缀。

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In depth · the introduction

把水加热,它沸腾成汽;把汽冷却,它又落回成雨——可范德瓦耳斯发现,气与液暗地里本是同一样东西,二者之间根本没有一条硬界线。

一道方程,两种状态

简单的气体定律 PV = RT,假装气体分子是不占地方、又彼此无视的小点。范德瓦耳斯把这两个假装都纠正了。分子确实要占一点地方,所以容器里头的空间,比看上去的要小。分子也确实彼此略微相吸,所以气体压向器壁时,比它本该的要轻柔一些。

只做这两处修正,奇妙的事就发生了:同一道方程,如今竟同时描述稀薄的气与致密的液。把气体压得够紧,公式本身就显示它塌缩成液。气与液,不再是两样不同的东西,而成了同一种物质的两副面孔。

一位莱顿的中学教师

范德瓦耳斯来得晚,也来自局外。他是荷兰的一名中学教师,物理大半自学,连参加大学考试都需特批——因为他不懂希腊文与拉丁文。1873 年他把这个想法写成博士论文时,已经三十六岁——而且用的是荷兰文,这几乎注定了世界会与它擦肩。

世界却没有。那个时代如山岳般的物理学家麦克斯韦,读到了它,叹服之余,据说为读原文而自学了荷兰文,并宣告:这位无名教师的名字,不久将跻身分子科学的最前列。三十七年后,1910 年,范德瓦耳斯正是凭这项工作,获颁诺贝尔物理学奖。

它为何重要

它解释了实验家方才撞见的一个谜:在某个温度——「临界温度」——之上,无论你压得多狠,气体都无法被压成液体。范德瓦耳斯的方程说清了为什么,甚至从他的理论预言:一旦以各自的临界点来度量,每种气体的行为都一模一样。正是这一条规则,精确地告诉了实验者,要冷到多冷、压到多紧——并在 1908 年,引出了氦的首次液化。

一间挤满人的屋子

想象一屋子人在走动。理想气体定律把他们当成幽灵:没有身体,从不相触。范德瓦耳斯加上两件真事。每个人其实都占地方,所以屋子比它的地板面积看上去要挤。而人们会与身旁的人轻轻牵手,所以这群人向墙壁外推的劲,要小一些。把他们挤得够紧,松散的人群会忽然凝成一个紧团——气体变作液体,全出自这两件再寻常不过的事实。

一条可交互的压强—体积曲线。一个滑块改变温度。临界温度之下,出现一道水平台阶,标出致密的液与稀薄的气在同一压强下共存之处;温度升高,台阶收窄为临界点,随后曲线变得平滑——成为一种流体。

它在故事里的位置

范德瓦耳斯建立在麦克斯韦与玻尔兹曼的动理论(热即运动中的分子)之上,也建立在安德鲁斯于二氧化碳中发现临界点之上。他的方程成了一切相变的范本,而他提出的那种微弱吸引,如今称作范德华力——正是让壁虎能爬上墙、也把 DNA 的横档维系在一起的那种力(见 watson-crick-1953)。当物理学家终于在一个世纪后精确理解了临界点,他们所完成的,正是范德瓦耳斯当年开启的那个问题。

The original document
Original source text
J. D. van der Waals · doctoral thesis, Leiden · 1873 · structural map; equation and Nobel citation quoted verbatim
The puzzle of 1873
Four years earlier Thomas Andrews had shown that carbon dioxide, warmed past 31 °C, can no longer be turned to liquid by any pressure — there is a critical temperature above which the line between gas and liquid simply disappears. The kinetic theory of Clausius and Maxwell, meanwhile, pictured a gas as a swarm of point-like particles that neither take up room nor attract one another. Van der Waals asked the obvious, unasked question: what if the molecules do both?
Two corrections to the ideal gas
He kept the ideal gas law PV = RT and mended it twice. First, the molecules occupy space, so the room left for them to move in is not V but V − b, where b is roughly the volume of the molecules themselves. Second, they pull on one another, so a molecule near the wall is tugged back inward and presses a little less hard; this lost pressure grows as the gas is squeezed, as a/V². Putting both together gives a single equation of state.
(P + a/V²)(V − b) = RT
Read as a cubic in V, this one formula can have, at a fixed temperature and pressure, three solutions: a small volume (the dense liquid), a large volume (the dilute gas), and a third, unstable root between them. Below the critical temperature the isotherm carries a backward wiggle — the famous van der Waals loop — and the flat line of real condensation cuts across it where the two lobes have equal area (Maxwell's rule, 1875). Raise the temperature and the three roots draw together; at the critical point they merge into one. Above it, only a single volume remains for each pressure: gas and liquid have become one continuous fluid.
One law for every gas
Measuring each quantity against its value at the critical point — π = P/P_c, φ = V/V_c, τ = T/T_c — makes the constants a, b and R vanish, leaving (π + 3/φ²)(3φ − 1) = 8τ. The same dimensionless curve now describes oxygen, water, and carbon dioxide alike: the law of corresponding states. It is this prediction that guided Kamerlingh Onnes in Leiden to the liquefaction of hydrogen and, in 1908, of helium.
[ … ]
Maxwell, reviewing the work, is said to have learned enough Dutch to read it in the original, and told the British Association that van der Waals's name would soon be “among the foremost in molecular science.” The 1910 Nobel Prize in Physics was awarded to van der Waals
for his work on the equation of state for gases and liquids.
Leiden · 1873