Salzmann Christoph G, Radaelli Paolo G, Finney John L, Mayer Erwin
Inorganic Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, UK.
Phys Chem Chem Phys. 2008 Nov 7;10(41):6313-24. doi: 10.1039/b808386j. Epub 2008 Sep 15.
Doped ice V samples made from solutions containing 0.01 M HCl (DCl), HF (DF), or KOH (KOD) in H(2)O (D(2)O) were slow-cooled from 250 to 77 K at 0.5 GPa. The effect of the dopant on the hydrogen disorder --> order transition and formation of hydrogen ordered ice XIII was studied by differential scanning calorimetry (DSC) with samples recovered at 77 K. DSC scans of acid-doped samples are consistent with a reversible ice XIII <--> ice V phase transition at ambient pressure, showing an endothermic peak on heating due to the hydrogen ordered ice XIII --> disordered ice V phase transition, and an exothermic peak on subsequent cooling due to the ice V --> ice XIII phase transition. The equilibrium temperature (T(o)) for the ice V <--> ice XIII phase transition is 112 K for both HCl doped H(2)O and DCl doped D(2)O. From the maximal enthalpy change of 250 J mol(-1) on the ice XIII --> ice V phase transition and T(o) of 112 K, the change in configurational entropy for the ice XIII --> ice V transition is calculated as 2.23 J mol(-1) K(-1) which is 66% of the Pauling entropy. For HCl, the most effective dopant, the influence of HCl concentration on the formation of ice XIII was determined: on decreasing the concentration of HCl from 0.01 to 0.001 M, its effectiveness is only slightly lowered. However, further HCl decrease to 0.0001 M drastically lowered its effectiveness. HF (DF) doping is less effective in inducing formation of ice XIII than HCl (DCl) doping. On heating at a rate of 5 K min(-1), kinetic unfreezing starts in pure ice V at approximately 132 K, whereas in acid doped ice XIII it starts at about 105 K due to acceleration of reorientation of water molecules. KOH doping does not lead to formation of hydrogen ordered ice XIII, a result which is consistent with our powder neutron diffraction study (C. G. Salzmann, P. G. Radaelli, A. Hallbrucker, E. Mayer, J. L. Finney, Science, 2006, 311, 1758). We further conjecture whether or not ice XIII has a stable region in the water/ice phase diagram, and on a metastable triple point where ice XIII, ice V and ice II are in equilibrium.
由含有0.01M HCl(DCl)、HF(DF)或KOH(KOD)的H₂O(D₂O)溶液制成的掺杂冰V样品在0.5GPa下从250K缓慢冷却至77K。通过差示扫描量热法(DSC)对在77K回收的样品研究了掺杂剂对氢无序→有序转变以及氢有序冰XIII形成的影响。酸掺杂样品的DSC扫描结果与常压下可逆的冰XIII⇌冰V相变一致,加热时由于氢有序冰XIII→无序冰V相变出现吸热峰,随后冷却时由于冰V→冰XIII相变出现放热峰。对于HCl掺杂的H₂O和DCl掺杂的D₂O,冰V⇌冰XIII相变的平衡温度(Tₒ)均为112K。根据冰XIII→冰V相变时250J mol⁻¹的最大焓变以及112K的Tₒ,计算出冰XIII→冰V转变的构型熵变为2.23J mol⁻¹ K⁻¹,这是鲍林熵的66%。对于最有效的掺杂剂HCl,确定了HCl浓度对冰XIII形成的影响:将HCl浓度从0.01M降至0.001M时,其有效性仅略有降低。然而,进一步将HCl降至0.0001M会大幅降低其有效性。HF(DF)掺杂在诱导冰XIII形成方面不如HCl(DCl)掺杂有效。以5K min⁻¹的速率加热时,纯冰V在约132K开始动力学解冻,而在酸掺杂的冰XIII中由于水分子重新取向加速,在约105K开始解冻。KOH掺杂不会导致氢有序冰XIII的形成,这一结果与我们的粉末中子衍射研究(C.G. Salzmann,P.G. Radaelli,A. Hallbrucker,E. Mayer,J.L. Finney,《科学》,2006年,311卷,1758页)一致。我们进一步推测冰XIII在水/冰相图中是否有稳定区域,以及在冰XIII、冰V和冰II处于平衡的亚稳三相点的情况。