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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >O2(~1DELTA)Quenching Mechanism in CVBasic Hydrogen Peroxide(Basic Deuterium Peroxide)Gas/Liquid Reaction and the Determination of O2(~1DELTA)/BHP(BDP)Interface Free Energy
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O2(~1DELTA)Quenching Mechanism in CVBasic Hydrogen Peroxide(Basic Deuterium Peroxide)Gas/Liquid Reaction and the Determination of O2(~1DELTA)/BHP(BDP)Interface Free Energy

机译:CV中的O2(〜1DELTA)猝灭机理碱性过氧化氢(BaO2)气/液反应及O2(〜1DELTA)/ BHP(BDP)界面自由能的测定

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In a jet-type singlet oxygen generator,we have studied the generation of O2(~1DELTA)via the reaction of chlorine gas with aqueous basic hydrogen peroxide(BHP)and with basic deuterium peroxide(BDP).The O2(~1DELTA)detachment yield with BDP is measured to be 72.5 ± 1.5%,merely 2.5% higher than that with BHP,despite a 10 times longer O2(~1DELTA)lifetime in BDP than in BHP.By a careful kinetic analysis of the Cl2+BHP(BDP)reactions,we found that the main resistance that prevents the nascent O2(~1DELTA)from escaping off the solution into the bulk gas flow does not lie in the liquid or gas phase,but in the gas/liquid interface.Thus,the seemingly weird experimental result can be justified by postulating a higher energy barrier at the O(~1DELTA)/BDP interface than that of the O2(~1DELTA)/BHP so as to detain the O2(~1DELTA)for a longer time in BDP.In fact,this postulation has been proved as follows:according to the physical model of Copeland and Zagidullin,the O2(~1DELTA)mass accommodation coefficient is calculated from our experimental solvation detachment yield to be ~4.0X 10~(-6)on the BHP surface and ~1.7X10~(-6)on the BDP surface.Then,based on the thermodynamics of phase equilibrium in dilute solutions,the corresponding Gibbs energy of O2(~1DELTA)at the BHP surface is computed as ~2.65X10~4 J/mol,and the value of O2(~1DELTA)at the BDP surface is ~2.86X10~4 J/mol.This higher O2(~1DELTA)/BDP interface energy barrier may result from both larger D2O molecular mass and stronger hydrogen bonding between D2O molecules in BDP solution.The present methodology can be further improved by using microwave-discharge production of O2(~1DELTA)so as to make direct measurements of its quenching probability.Hence,more key thermodynamic and kinetic information about the O2/aqueous electrolyte solution interfaces will be made available.Work along this line is now under way.
机译:在喷射型单重态氧气发生器中,我们研究了氯气与碱性过氧化氢水溶液(BHP)和碱性过氧化氢氘(BDP)反应生成O2(〜1DELTA)的方法。尽管BDP的O2(〜1DELTA)寿命比BHP长10倍,但BDP的产率为72.5±1.5%,仅比BHP高2.5%。通过仔细的动力学分析Cl2 + BHP(BDP) )反应,我们发现阻止新生O2(〜1DELTA)逸出溶液进入大气流的主要阻力并不在于液相或气相,而在于气/液界面。可以通过假设O(〜1DELTA)/ BDP界面的能垒比O2(〜1DELTA)/ BHP的能垒更高,以便在BDP中将O2(〜1DELTA)保留更长的时间来证明怪异的实验结果。实际上,该假设已被证明如下:根据Copeland和Zagidullin的物理模型,O2(〜1DELTA)质量调节系数根据我们的实验溶剂化离解率计算出的有效值是BHP表面上的〜4.0X 10〜(-6)和BDP表面上的〜1.7X10〜(-6)。然后,基于稀溶液中相平衡的热力学,BHP表面的O2(〜1DELTA)对应的吉布斯能量经计算为〜2.65X10〜4 J / mol,BDP表面的O2(〜1DELTA)值为〜2.86X10〜4 J / mol。较高的O2(〜1DELTA)/ BDP界面能垒可能是由于BDP溶液中较大的D2O分子质量和较强的D2O分子之间的氢键所致。通过微波放电产生O2(〜1DELTA)可以进一步改进本方法。因此,将提供有关O2 /电解质水溶液界面的更多重要热力学和动力学信息。

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