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Degradation of refractory organic compounds from dinitrodiazophenol containing industrial wastewater through UV/H2O2 and UV/PS processes

机译:通过UV / H 2 O 2和UV / PS工艺从含二硝基二唑苯酚的耐火有机化合物的降解

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In this study, refractory organic compounds from dinitrodiazophenol (DDNP) containing industrial wastewater were degraded through two ultraviolet (UV)-based advanced oxidation processes: UV/hydrogen peroxide (UV/H2O2) and UV/potassium persulfate (UV/PS) processes. In both processes, the synergistic effects, operational parameters (i.e., oxidant dosage and initial pH value), and pseudo first-order constant k were systematically studied. Moreover, the reactive oxygen species formed in the UV/H2O2 and UV/PS processes were identified, and the degradation of refractory organic compounds was characterized through UVvisible spectra analysis. The improvement in biodegradability of DDNP industrial wastewater after treatment by different processes was compared. Both the UV/H2O2 (synergistic coefficient F = 61.34) and UV/PS (synergistic coefficient F = 54.85) processes showed significant, highly synergistic effects. The increase in oxidant dosage was beneficial in organic compound removal in both the UV/H2O2 and UV/PS processes, but excessive H2O2 showed a stronger inhibition of the increase in organic compound removal than that in the UV/PS process. In addition, an acidic environment was more conducive to organic compound degradation in the UV/H2O2 process, whereas the initial pH value had less of an influence on the UV/PS process. Under optimal conditions for the UV/H2O2 and UV/PS processes, the CN and COD removal efficiencies were 99.71%, 66.35%, 99.69%, and 70.81%, respectively, and the k values for COD removal were 0.0804 and 0.0824 min-1. Tests to identify reactive oxygen species showed that the hydroxyl radical was the predominant oxidizing species in the UV/H2O2 process, whereas the hydroxyl and sulfate radicals were both identified in the UV/PS process, and the sulfate radical contributed the most to the degradation of organic compounds. In addition, spectrum analysis revealed that the complex structure (e.g., benzene ring, nitro group, and diazo group) of refractory organic compounds from DDNP industrial wastewater was effectively destroyed by the UV/H2O2 and UV/ PS processes, and both processes improved the biodegradability (biochemical oxygen demand for 5 days/chemical oxygen demand (BOD5/COD)) of DDNP industrial wastewater from 0.052 to 0.665 and 0.717, respectively. Overall, both the UV/ H2O2 and UV/PS processes effectively degraded the refractory organic compounds from DDNP industrial wastewater, and the UV/PS process exhibited a higher organic compound removal efficiency and better applicability.
机译:在该研究中,通过两种紫外(UV)的高级氧化方法,二硝基二唑(DDNP)的难治性有机化合物(DDNP)降解:UV /氢过氧化氢(UV / H2O2)和UV /钾过硫酸钾(UV / PS)方法。在这种过程中,系统地研究了协同效应,操作参数(即氧化剂剂量和初始pH值)和伪第一阶常数k。此外,鉴定了在UV / H 2 O 2和UV / PS过程中形成的反应性氧物质,并通过UV可见的光谱分析表征了难熔有机化合物的降解。比较了不同方法治疗后DDNP工业废水的生物降解性的改善。 UV / H 2 O 2(协同系数F = 61.34)和UV / PS(协同系数F = 54.85)过程显示出显着,高度协同的效果。氧化剂剂量的增加有利于UV / H 2 O 2和UV / PS过程中的有机化合物去除,但过量的H 2 O 2显示出比UV / PS过程中的有机化合物的增加较强的抑制。此外,酸性环境更有利于UV / H 2 O 2过程中的有机化合物降解,而初始pH值对UV / PS过程的影响较小。在UV / H 2 O 2和UV / PS过程的最佳条件下,CN和COD去除效率分别为99.71%,66.35%,99.69%和70.81%,鳕鱼的k值为0.0804和0.0824 min-1 。鉴定反应性氧物质的试验表明,羟基自由基是UV / H 2 O 2工艺中的主要氧化物质,而羟基和硫酸根在UV / PS过程中均鉴定,并且硫酸盐基团最大限度地促成了降解有机化合物。此外,光谱分析显示,通过UV / H 2 O 2和UV / PS工艺有效地破坏了DDNP工业废水的难治性有机化合物的复杂结构(例如,苯环,硝基和重氮基),并且两种过程改善了DDNP工业废水的生物降解性(生化氧需求5天/化学需氧量(BOD5 / COD)分别为0.052至0.665和0.717。总的来说,UV / H 2 O 2和UV / PS过程都有效地降解了DDNP工业废水的耐火有机化合物,并且UV / PS过程表现出更高的有机化合物去除效率和更好的适用性。

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