“Debye–Hückel theory”的概念、定义、翻译、参考文献-科学参考

Debye–Hückel theory

Physics

A theory to explain the nonideal behaviour of electrolytes, published in 1923 by Peter Debye (1884–1966) and Erich Hückel (1896–1980). It assumes that electrolytes in solution are fully dissociated and that nonideal behaviour arises because of electrostatic interactions between the ions. The theory shows how to calculate the extra free energy per ion resulting from such interactions, and consequently the activity coefficient. It gives a good description of nonideal electrolyte behaviour for very dilute solutions, but cannot be used for more concentrated electrolytes.

Chemistry

A theory to explain the nonideal behaviour of electrolytes, published in 1923 by Peter Debye and Erich Hückel (1896–1980). It assumes that electrolytes in solution are fully dissociated and that nonideal behaviour arises because of electrostatic interactions between the ions. The theory shows how to calculate the extra free energy per ion resulting from such interactions, and consequently the activity coefficient. It gives a good description of nonideal electrolyte behaviour for very dilute solutions, but cannot be used for more concentrated electrolytes.

单词	Debye–Hückel theory
释义	Debye–Hückel theory Physics A theory to explain the nonideal behaviour of electrolytes, published in 1923 by Peter Debye (1884–1966) and Erich Hückel (1896–1980). It assumes that electrolytes in solution are fully dissociated and that nonideal behaviour arises because of electrostatic interactions between the ions. The theory shows how to calculate the extra free energy per ion resulting from such interactions, and consequently the activity coefficient. It gives a good description of nonideal electrolyte behaviour for very dilute solutions, but cannot be used for more concentrated electrolytes. Chemistry A theory to explain the nonideal behaviour of electrolytes, published in 1923 by Peter Debye and Erich Hückel (1896–1980). It assumes that electrolytes in solution are fully dissociated and that nonideal behaviour arises because of electrostatic interactions between the ions. The theory shows how to calculate the extra free energy per ion resulting from such interactions, and consequently the activity coefficient. It gives a good description of nonideal electrolyte behaviour for very dilute solutions, but cannot be used for more concentrated electrolytes.
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