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An analytical model based on experimental data for the self-hydrolysis kinetics of aqueous sodium borohydride.

机译:基于实验数据的硼氢化钠水溶液的自水解动力学分析模型。

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摘要

The objective of this work is to determine the self-hydrolysis kinetics of sodium borohydride (NaBH4) in a solution with liquid water (H 2O) for hydrogen (H2) generation and storage purposes. In order to be able to derive two semi-global rate expressions, an extensive series of batch process experiments was performed in a glass flask where the following parameters were systematically varied: solution temperature varied from 298 K (25°C) to 348 K (75°C), NaBH4 concentration ranged from 0.5 wt% to 25.0 wt%, and the concentration of the hydrolysis stabilizer sodium hydroxide (NaOH) varied from 0.0 wt% to 4.0 wt%, which corresponds to initial solution pH values ranging from 9.5 to 12.95. Transient hydrogen generation rates and transient solution pH were measured during hydrolysis. Based on the data collected, the decomposition rate for NaBH4 when the effect of the transition period diminishes is found to be: -dNaBH4 dt=A1˙e 49860J/molRT NaBH4 H+0.788 Where A1=1.72x109 1s Lmol0.788 [NaBH4] represents the NaBH4 concentration in units of moles per kilogram of solution, [H+] represents the concentration of the hydrogen ion, H+, in units of moles per liter of water, R in the Arrhenius term is the universal gas constant and T is temperature in Kelvin. The expression for the rate of change of [H +] (or equivalently pH level) is: -dH+ dt=A2f NaBH4O ˙e-7930J/m olRT˙e -4.5291-NaB H4NaBH 4O H+b 2f&parl0;&sqbl0;NaBH4&sqbr0;O&parr0; Where A2fNaBH4 O= -2.236˙NaBH4 O+36.6081 sL molb2 b2f&parl0;&sqbl0;NaBH4&sqbr0; O&parr0;=0.0973˙&sqbl0;NaBH4&sqbr0; O-2.763 The quantity [NaBH4]O represents the initial concentration of sodium borohydride and f is symbolic for a function. In principle, given initial conditions (temperature, NaBH4 concentration and H+ concentration), the two quasi-global coupled equations can be integrated to obtain the transient time history of H2 (or NaBH4) and solution pH (or H+). The model transient hydrogen generation rate and transient pH trends were compared with experimental data. Good agreement between analytical and experimental data was reached for many conditions, especially for elevated solution pH values, levels at which NaBH4 solutions are used practically.
机译:这项工作的目的是确定硼氢化钠(NaBH4)在具有液态水(H 2O)的溶液中用于氢(H2)生成和存储的自水解动力学。为了能够得出两个半全局速率表达式,在玻璃烧瓶中进行了一系列批量过程实验,其中系统地更改了以下参数:溶液温度从298 K(25°C)到348 K( 75°C),NaBH4浓度范围为0.5重量%至25.0重量%,水解稳定剂氢氧化钠(NaOH)的浓度范围为0.0重量%至4.0重量%,这对应于溶液的初始pH值范围为9.5至0.5 12.95。在水解过程中测量了瞬态氢的生成速率和瞬态溶液的pH值。根据收集的数据,发现过渡期影响减小时,NaBH4的分解速率为:-dNaBH4 dt = A1e 49860J / molRT NaBH4 H + 0.788其中A1 = 1.72x109 1s Lmol0.788 [NaBH4]代表NaBH4的浓度,以每千克溶液的摩尔数为单位; [H +]代表氢离子的浓度,H +,以每升水的摩尔数为单位,Arrhenius术语中的R为通用气体常数,T为温​​度。开尔文[H +](或相当的pH水平)的变化率的表达式为:-dH + dt = A2f NaBH4O·e-7930J / m olRT·e -4.5291-NaB H4NaBH 4O H + b 2f&parl0;&sqbl0; NaBH4&sqbr0 ; O&parr0;其中A2fNaBH4 O = -2.236&NaBH4 O + 36.6081 sL molb2 b2f&parl0;&sqbl0; NaBH4&sqbr0; O&parr0; = 0.0973˙&sqbl0; NaBH4&sqbr0; O-2.763 [NaBH4] O的量表示硼氢化钠的初始浓度,f表示功能。原则上,在给定初始条件(温度,NaBH4浓度和H +浓度)的情况下,可以将这两个准全局耦合方程进行积分以获得H2(或NaBH4)和溶液pH(或H +)的瞬态时间历史。将模型的瞬时氢生成速率和瞬时pH趋势与实验数据进行了比较。在许多条件下,尤其是在溶液pH值升高(实际使用NaBH4溶液的水平)下,分析数据与实验数据之间达成了良好的一致性。

著录项

  • 作者

    Bartkus, Tadas Patrick.;

  • 作者单位

    Case Western Reserve University.;

  • 授予单位 Case Western Reserve University.;
  • 学科 Engineering Mechanical.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 183 p.
  • 总页数 183
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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