电离辐射对铁胶体溶液稳定性影响规律的研究

L. R. Merinova, L. Shiyan, G. Remnev, A. Stepanov, M. Kaikanov, D. Voyno
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引用次数: 2

摘要

本文研究了脉冲电子辐射对胶体铁溶液稳定性的影响。这项工作是在标准测试溶液上进行的,这些溶液对应于真实的天然水和废水的化学成分。采用TEA-500脉冲加速器进行辐照,电子能量500 keV,脉冲持续时间60 ns。剂量是用硝酸钾来计算的,硝酸钾被推荐用于测量脉冲电子辐射的剂量。辐射标准试验溶液中铁、硅、腐殖质离子的相关系数分别为5.6:20:2.2 mg/l。溶液的辐照范围为0.6 ~ 5.0 Mrad。通过初始溶液和辐照溶液中铁的色度和浓度的变化来估计辐照效率。辐照后铁浓度和溶液色度的下降表明胶体溶液和Fe(OH)3混凝污泥的稳定性受到了破坏。为了解释辐射与胶体粒子的相互作用,考虑了水的辐射分解机制,因为大部分电离辐射能量被消耗在与水的相互作用中,形成了大谱的辐射分解产物。本文给出了水合电子与胶体粒子的相互作用机理,理由是水合电子的寿命比H和OH自由基长得多,形成的辐射化学输出大,相当于每100 eV 3.3÷3.5个离子。水合电子的寿命为2.3*10-4 s。此外,水合电子的尺寸为0.38 nm,远小于胶束的尺寸,由于这些因素,它与胶束核相互作用。根据文献数据,电子向胶束核转移的机制伴随着双电层的破坏,形成Fe(OH)3污泥的胶束被破坏,这是在标准测试胶体溶液的电子束辐照过程中观察到的。本文介绍了硝酸离子对标准试验溶液中铁离子颜色和浓度变化动力学的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation of the laws of ionizing radiation effect on the stability of the colloidal solutions of iron
In the paper, the effect of the pulse electron radiation on the stability of the colloidal iron solutions is studied. The work is performed on the standard test solutions which correspond to the real natural and waste water regarding their chemical composition. The irradiation was performed using the pulse accelerator TEA-500 with the electron energy 500 keV and pulse duration 60 ns. The dose was calculated using the potassium nitrate recommended for measuring the dose of the pulse electron radiation. The standard test solution used for radiation contained iron, silicon and humic substances ions in the correlation 5.6:20:2.2 mg/l, respectively. The solutions were subjected to radiation within the range of 0.6-5.0 Mrad. The efficiency of radiation was estimated by the variation in iron chromaticity and concentration in the initial and irradiated solution. The decrease in iron concentration and solution chromaticity after the radiation indicates the violation of the stability of the colloidal solution and the Fe(OH)3 coagulation sludge. To explain the interaction of the radiation with the colloidal particles, the water radiolysis mechanism was considered, since the most of the ionizing radiation energy is consumed for the interaction with the water forming a large spectrum of radiolysis products. In the paper we offer the interaction mechanism of hydrated electron and the colloidal particles on the ground that the hydrated electron has a much longer life compared to H and OH radicals and is formed with a large radiation-chemical output which is equal to 3.3÷3.5 ions per 100 eV. The lifetime of the hydrated electron is 2.3*10-4 s. Besides, the size of the hydrated electron is 0.38 nm that is much less than the size of micelle and because of these factors it interacts with the micelle nucleus. According to the literature data, the mechanism of the electron transfer to the micelle nucleus is accompanied with the violation of the double electrical layer, the destruction of the micelle forming the Fe(OH)3 sludge that was observed during the electron beam irradiation of the standard test colloidal solutions. In the paper we present the results on the effect of the ion nitrate on the kinetics of the variation in iron ion color and concentration in the standard test solution.
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