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首页> 外文期刊>Chemical engineering journal >Synergy of sulfate and hydroxyl radicals in UV/S2O8~(2-)/H2O2 oxidation of iodinated X-ray contrast medium iopromide
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Synergy of sulfate and hydroxyl radicals in UV/S2O8~(2-)/H2O2 oxidation of iodinated X-ray contrast medium iopromide

机译:碘化X射线造影剂碘化丙啶的UV / S2O8〜(2-)/ H2O2氧化中硫酸根和羟基自由基的协同作用

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摘要

The degradation of iodinated X-ray contrast medium, iopromide, by UV irradiation with the assistance of combined oxidants of S2O8~(2-) and H2O2 has been investigated. The effects of various parameters, including different wavelengths of UV irradiation, UV intensities, initial solution pH levels, dosages of oxidants, dosing sequence, and the presence of non-target organic matters, have been evaluated. The iopromide decay follows pseudo-first-order kinetics. The UV at 254 nm exhibits higher decay rate of iopromide than the others (300 and 350 nm) due to stronger photon energy of 254 nm and the relatively higher absorptivity of S2O8~(2-), H2O2 and iopromide nearby this wavelength. Optimum pH level was determined to be around 4.34. The mechanism is complicated because of the involvement of the scavenging, recombination, self-decomposition and/or stability of the involved oxidant (S2O8~(2-) and H2O2) and radicals (SO4~(·-) and HO~·) as discussed in the paper. Iopromide decay rate is linearly proportional to the [S2O8~(2-)], however a nonlinear-optimal rate was observed by varying [H2O2] due to the formation of weaker radicals via overdosing of H2O2. Additionally, the sequential addition of S2O8~(2-) to UV/H2O2 or H2O2 to UV/S2O8~(2-) was found no better than the UV/S2O8~(2-)/H2O2. This is because the quenching of already formed SO4~(·-) by newly added H2O2 (or vice versa the quenching of HO~· by S2O8~(2-)). The simultaneous addition of S2O8~(2-) and H2O2, however, will slightly delay the generation rates of S04~(·-) and OH~· due to the competition of photons between S2O8~(2-) and H2O2, which can reduce both the radical-scavenging reactions and the peak radical concentration in the solution, thus maximizing the utilization of precious radicals. The presence of non-target organics, especially the humic acid, in the UV/S2O8~(2-) /H2O2 process will quench the radicals, a pre-treatment is recommended to lessen this problem in real application.
机译:研究了在S2O8〜(2-)和H2O2的混合氧化剂的辅助下,通过紫外线辐照降解碘化X射线造影剂碘普罗胺。已经评估了各种参数的影响,包括不同波长的紫外线照射,紫外线强度,初始溶液的pH值,氧化剂的剂量,加药顺序以及非目标有机物的存在。碘化丙啶的衰变遵循伪一级动力学。 254 nm处的UV表现出碘普罗胺的衰减速率高于其他波长(300和350 nm),这是因为254 nm的光子能量更强,并且在该波长附近的S2O8〜(2-),H2O2和碘普罗胺的吸收率相对较高。确定最佳pH水平为约4.34。由于涉及的氧化剂(S2O8〜(2-)和H2O2)和自由基(SO4〜(·-)和HO〜·)的清除,重组,自分解和/或稳定性的参与,其机理很复杂。在本文中讨论。碘溴化物的衰减速率与[S2O8〜(2-)]成线性比例关系,但是由于过量加入H2O2而形成较弱的自由基,通过改变[H2O2]可以观察到非线性最佳速率。另外,发现将S 2 O 8-(2-)顺序添加至UV / H 2 O 2或将H 2 O 2添加至UV / S 2 O 8-(2-)中并不比UV / S 2 O 8-(2-)/ H 2 O 2好。这是因为通过新添加的H2O2淬灭已形成的SO4〜(-)(反之亦然,通过S2O8〜(2-)淬灭HO〜·)。然而,由于光子在S2O8〜(2-)和H2O2之间的竞争,同时添加S2O8〜(2-)和H2O2会稍微延迟S04〜(·-)和OH〜·的生成速率,同时减少自由基清除反应和溶液中的峰值自由基浓度,从而最大限度地利用了宝贵的自由基。 UV / S2O8〜(2-)/ H2O2过程中存在非目标有机物,特别是腐殖酸会淬灭自由基,建议进行预处理以减少实际应用中的此问题。

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