Fukada H, Takahashi K
Laboratory of Biophysical Chemistry, College of Agriculture, Osaka Prefecture University, Sakai, Japan.
Proteins. 1998 Nov 1;33(2):159-66.
Enthalpy and heat capacity changes for the deprotonation of 18 buffers were calorimetrically determined in 0.1 M potassium chloride at temperatures ranging from 5 to 45 degrees C. The values of the dissociation constant were also determined by means of potentiometric titration. The enthalpy changes for the deprotonation of buffers, except for the phosphate and glycerol 2-phosphate buffers, were found to be characterized by a linear function of temperature. The enthalpy changes for the second dissociation of phosphate and glycerol 2-phosphate where divalent anion is formed on dissociation were fitted with the second order function of temperature rather than the first order. Temperature dependence of buffer pH calculated by using the enthalpy and heat capacity changes obtained was in good agreement with the temperature variation of the pH values actually measured in the temperature range between 0 and 50 degrees C for all the buffers studied. On the basis of the results obtained, a numeric table showing the temperature dependence of pK values for the 18 buffers is presented.
通过量热法测定了18种缓冲剂在0.1 M氯化钾中、5至45摄氏度温度范围内去质子化的焓变和热容变化。解离常数的值也通过电位滴定法测定。发现除磷酸盐和甘油2 - 磷酸缓冲剂外,缓冲剂去质子化的焓变具有温度的线性函数特征。磷酸盐和甘油2 - 磷酸第二次解离形成二价阴离子时的焓变,拟合的是温度的二阶函数而非一阶函数。利用所获得的焓变和热容变化计算得到的缓冲剂pH值的温度依赖性,与在0至50摄氏度温度范围内对所有研究缓冲剂实际测量的pH值变化情况高度吻合。基于所获得的结果,给出了一个显示18种缓冲剂pK值温度依赖性的数值表。