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Vol.106,no.14,2006

机译:Vol.106,No.14,2006

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摘要

Based on the Planck-Benzinger thermal work function using Chun's method,the innate temperature-invariant enthalpy at 0 K,DELTA H_o(T_o),for the condensation of water vapor as well as the dimer,trimer,tetramer,and pentamer form in the vapor phase,was determined to be 0.447 kcal mol~(-1) for vapor,1.127 for the dimer,0.555 for the trimer,0.236 for the tetramer,and 0.079 kcal mol~(-1) for the pentamer using AG(T) data reported by Kell et al.in 1968 and Kell and McLaurin in 1969.These results suggest that the predominant dimeric form is the most stable of these n-mers.Using Nemethy and Scheraga's 1962 data for the Helmholtz free energy of liquid water,the value of DELTA H_o(T_o) was determined to be 1.21 kcal mol~(-1).This is very dose to the value for the energy of the hydrogen bond E_H of 1.32 kcal mol~(-1) reported by Nemethy and Scheraga,using statistical thermodynamics.It seems clear that very little energy is required for interconversion between the hypothetical supercooled water vapor and glassy water at 0 K.A hypothetical supercooled water vapor at 0 K is apparently almost as highly associated as glassy water at that temperature,suggesting a dynamic equilibrium between vapor and liquid.This water vapor condensation is highly similar in its thermodynamic behavior to that of sequence-specific pairwise (dipeptide) hydrophobic interaction,except that the negative Gibbs free energy change minimum at (T_s),the thermal setpoint for vapor condensation,where T DELTA S=0,occurs at a considerably lower temperature,270 K (below 0 deg C) compared with approx 350 K.The temperature of condensation (T_(cpmd)> at which DELTA G(T)=0,where water vapor begins to condense,was found to be 383 K.In the case of a sequence-specific pairwise hydrophobic interaction,the melting temperature,(T_m),where DELTA G(T_m)=0 was found to be 460 K.Only between two temperature limits,(T_h)=99 K and =383 K,where DELTA G(T_(cond))=0,is the net chemical driving force favorable for polymorphism of glassy water and hypothetical supercooled water vapor.Analysis of the water vapor condensation process based on the Planck-Benzinger thermal work function confirms that a thermodynamic molecular switch occurs at 10.K,wherein a change of sign in [DE;TA C_p(T)]_(cond) leads to a true negative minimum in the Gibbs free energy of vapor condensation,and hence a maximum in the related equilibrium constant,K_(cond).
机译:基于Chun方法的Planck-Benzinger热功函数,在0 K时固有的温度不变焓DELTA H_o(T_o),用于冷凝水蒸气以及二聚体,三聚体,四聚体和五聚体形式。使用AG(T)测定气相的蒸气相为0.447 kcal mol〜(-1),二聚体为1.127,三聚体为0.555,四聚体为0.236,五聚体为0.079 kcal mol〜(-1)。由Kell等人在1968年和Kell和McLaurin在1969年报道的数据表明,主要的二聚体形式是这些n-mer中最稳定的形式。根据Nemethy和Scheraga的1962年数据,液态水的亥姆霍兹自由能DELTA H_o(T_o)的值确定为1.21 kcal mol〜(-1),这与Nemethy和Scheraga报道的氢键E_H的能量值为1.32 kcal mol〜(-1)非常吻合,显然,假设的过冷水蒸气之间的相互转化几乎不需要能量或0 KA的玻璃状水,假设0 K的过冷水蒸气与该温度下的玻璃状水几乎高度缔合,暗示着水蒸气与液体之间的动态平衡。这种水蒸气的凝结与热力学上的相似。序列特定的成对(二肽)疏水相互作用,不同的是,负吉布斯自由能在(T_s)最小变化,这是蒸汽冷凝的热设定点,其中T DELTA S = 0在相当低的温度下发生,270 K(低于0摄氏度(约350 K)。冷凝温度(T_(cpmd)>,其中DELTA G(T)= 0,水蒸气开始冷凝,发现温度为383K。特定的成对疏水相互作用,熔融温度(T_m),其中DELTA G(T_m)= 0为460 K.仅在两个温度范围之间(T_h)= 99 K和 = 383 K ,其中DELTA G(T_(cond))= 0,是对多晶型物有利的净化学驱动力m的玻璃状水和假设的过冷水蒸气。基于普朗克-本辛格热功函数的水蒸气冷凝过程分析表明,热力学分子转换发生在10.K,其中[DE; TA C_p( T)] _(cond)导致蒸气凝结的吉布斯自由能的真负极小值,因此导致相关平衡常数K_(cond)的最大值。

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