搅拌速度对环境空气冷等离子体亚甲基蓝褪色动力学的影响

IF 1.5 4区 化学 Q4 CHEMISTRY, PHYSICAL International Journal of Chemical Kinetics Pub Date : 2024-07-03 DOI:10.1002/kin.21755
Alessandra Mbroczkoski Pereira, Péricles Inácio Khalaf
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The calculated thermodynamic activation parameters comprised: <i>E<sub>a</sub></i> = 7.96 kJ mol<sup>−1</sup>, <i>ΔH</i><sup>‡</sup> = +5.53 kJ mol<sup>−1</sup>, <i>ΔS</i><sup>‡</sup> = −253.23 J K<sup>−1</sup> mol<sup>−1</sup>, and <i>ΔG</i><sup>‡</sup> = +79.77 kJ mol<sup>−1</sup> (100 rpm); and <i>E<sub>a</sub></i> = 12.94 kJ mol<sup>−1</sup>, Δ<i>H</i><sup>‡</sup> = +13.78 kJ mol<sup>−1</sup>, <i>ΔS</i><sup>‡</sup> = −239.06 J K<sup>−1</sup> mol<sup>−1</sup>, and <i>ΔG</i><sup>‡</sup> = +80.58 kJ mol<sup>−1</sup>, (750 rpm). The lowest <i>E<sub>a</sub></i> and <i>ΔG</i><sup>‡</sup> values at 100 rpm reinforced lower agitation favoring the reaction. The study demonstrated a linear decay of the reaction rate constant with the square root of ionic strength. 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引用次数: 0

摘要

本研究调查了使用环境空气冷等离子体的亚甲基蓝(MB)褪色动力学,重点是搅拌速度(100 和 750 rpm)的影响。研究发现了甲基溴褪色的伪一阶动力学,并确定了 35.00°C 和 100 rpm 的最佳条件。这些参数最大限度地缩短了半衰期,与观察到的 kobs 值相关。pH 值呈下降趋势,在 750 rpm 时更为明显,这是由于酸性氮物种(HNO3 和 HNO2)的产生增加,对染料褪色产生了不利影响。与此同时,由于等离子体产生活性物质并溶解于水相中,电导率上升导致电解质浓度增加。计算得出的热力学活化参数包括Ea = 7.96 kJ mol-1,ΔH‡ = +5.53 kJ mol-1,ΔS‡ = -253.23 J K-1 mol-1,ΔG‡ = +79.77 kJ mol-1(100 rpm);以及 Ea = 12.94 kJ mol-1,ΔH‡ = +13.78 kJ mol-1,ΔS‡ = -239.06 J K-1 mol-1,ΔG‡ = +80.58 kJ mol-1,(750 转/分)。100 rpm 时的 Ea 和 ΔG‡ 值最低,这说明较低的搅拌有利于反应的进行。研究表明,反应速率常数随离子强度的平方根呈线性衰减。除了负活化熵和适度活化焓之外,这一结果还提出了过渡态形成的决定性步骤,涉及溶解电子和质子化底物之间的关联步骤。在 35.00°C 和 100 转/分钟的条件下,染料褪色率和能量产率达到最佳,分别为 97.2% 和 3.371 × 10-2 g kW-1 h-1。
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Effect of agitation speed on methylene blue discoloration kinetics via ambient air cold plasma

This research investigates the kinetics of methylene blue (MB) discoloration using ambient air cold plasma, with a focus on the impact of agitation speed (100 and 750 rpm). The study revealed pseudo-first-order kinetics for MB discoloration, pinpointing optimal conditions at 35.00°C and 100 rpm. These parameters minimized half-life times, correlated with observed kobs values. A decreasing pH trend, more pronounced at 750 rpm, was attributed to increased acidic nitrogen species (HNO3 and HNO2) production, adversely affecting dye discoloration. Concurrently, enhanced electrolyte concentration was noted from rising conductivity due to plasma production of reactive species followed by solubilization in the aqueous phase. The calculated thermodynamic activation parameters comprised: Ea = 7.96 kJ mol−1, ΔH = +5.53 kJ mol−1, ΔS = −253.23 J K−1 mol−1, and ΔG = +79.77 kJ mol−1 (100 rpm); and Ea = 12.94 kJ mol−1, ΔH = +13.78 kJ mol−1, ΔS = −239.06 J K−1 mol−1, and ΔG = +80.58 kJ mol−1, (750 rpm). The lowest Ea and ΔG values at 100 rpm reinforced lower agitation favoring the reaction. The study demonstrated a linear decay of the reaction rate constant with the square root of ionic strength. This result, besides the negative activation entropy and moderate activation enthalpy led to a proposition to the determinant step for the transition state formation, involving an associative step between a solvated electron and the protonated substrate. The optimal dye discoloration rate and energy yield were observed at 35.00°C and 100 rpm, with values of 97.2% and 3.371 × 10−2 g kW−1 h−1, respectively.

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来源期刊
CiteScore
3.30
自引率
6.70%
发文量
74
审稿时长
3 months
期刊介绍: As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.
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