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Flow effects on phenol degradation and sonoluminescence at different ultrasonic frequencies

机译:不同超声频率下酚类降解和声发炎的流动影响

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Current literature shows a direct correlation between the sonochemical (SC) process of iodide oxidation and the degradation of phenol solution. This implies phenol degradation occurs primarily via oxidisation at the bubble surface. There is no work at present which considers the effect of fluid flow on the degradation process. In this work, parametric analysis of the degradation of 0.1 mM phenol solution and iodide dosimetry under flow conditions was undertaken to determine the effect of flow. Frequencies of 44, 300 and 1000 kHz and flow rates of 0, 24, 228 and 626 mL/min were applied with variation of power input, air concentration, and surface stabilisation. Phenol degradation was analysed using the 4-aminoantipyrine (4-AAP) method, and sonoluminescence (SL) images were evaluated for 0.1, 20 and 60 mM phenol solutions. Flow, at all frequencies under certain conditions, could augment phenol degradation. At 300 kHz there was excellent correlation between phenol degradation and dosimetry indicating a SC process, here flow acted to increase bubble transience, fragmentation and radical transfer to solution. At 300 kHz, although oxidation is the primary phenol degradation mechanism, it is limited, attributed to degradation intermediates which reduce OH radical availability and bubble collapse intensity. For 44 and 1000 kHz there was poor correlation between the two SC processes. At 44 kHz (0.01 mM), there was little to suggest high levels of intermediate production, therefore it was theorised that under more transient bubble conditions additional pyrolytic degradation occurs inside the bubbles via diffusion/nanodroplet injection mechanisms. At 1000 kHz, phenol degradation was maximised above all other systems attributed to increased numbers of active bubbles combined with the nature of the ultrasonic field. SL quenching, by phenol, was reduced in flow systems for the 20 and 60 mM phenol solutions. Here, where the standing wave field was reinforced, and bubble localisation increased, flow and the intrinsic properties of phenol acted to reduce coalescence/clustering. Further, at these higher concentrations, and in flow conditions, the accumulation of volatile phenol degradation products inside the bubbles are likely reduced leading to an increase SL.
机译:目前的文献显示了碘化物氧化和酚溶液的降解的Sonochemical(SC)过程之间的直接相关性。这意味着酚类降解主要通过气泡表面氧化发生。目前没有工作,这考虑了流体流动对降解过程的影响。在这项工作中,对0.1mM酚溶液的降解和碘化物剂量测定的参数分析进行了流动条件,以确定流动的效果。施加44,300和1000kHz的频率和0,24,228和626ml / min的流速,具有功率输入,空气浓度和表面稳定性的变化。使用4-氨基丙氨酸(4-AAP)方法分析酚劣化,并评估SonoL发辐射辐射性(SL)图像0.1,20和60mM酚溶液。在某些条件下的所有频率下,流动可能会增加酚类劣化。在300kHz时,酚劣化和剂量测定的表明SC过程之间存在良好的相关性,这里的流动作用以增加泡沫转诊,碎裂和自由基转移到溶液中。在300kHz时,虽然氧化是初级酚类降解机制,但它受到限制,归因于降低oh自由基可用性和泡沫塌陷强度的降解中间体。对于44和1000kHz,两个SC过程之间的相关性差。在44 kHz(0.01mm)时,几乎没有提出高水平的中间生产,因此它被理解,在更多的瞬时气泡条件下通过扩散/纳米射线喷射机构在气泡内发生额外的热解劣化。在1000 kHz,苯酚降解最大化以上所有其他系统归因于与超声波场的性质组合的活性气泡增加。通过苯酚的SL猝灭,在20和60mM酚溶液的流动系统中减少。这里,在增强驻波场的情况下,泡沫定位增加,流动和苯酚的内在性能作用以减少聚结/聚类。此外,在这些较高的浓度下,在流动条件下,气泡内部的挥发性酚类降解产物的积累可能降低导致增加SL。

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