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首页> 外文期刊>Environmental Science and Pollution Research >Kinetics and mechanism of radium-isotopes dissolution in TENORM scale waste associated with petroleum production using certain organic carbon source: lactic acid solution-case study
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Kinetics and mechanism of radium-isotopes dissolution in TENORM scale waste associated with petroleum production using certain organic carbon source: lactic acid solution-case study

机译:使用某些有机碳源与石油生产相关的radium-Isotopes溶解的动力学和机制:使用某些有机碳源:乳酸解决方案研究

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摘要

The present study is conducted to explore the dissolution as inferred from the kinetic mechanism for radium-isotopes (Ra-228,Ra-226, and(224)Ra) in the TENORM scale waste deposited in oilfield pipes and equipment, Gulf of Suez, Egypt. The main efficiency factors for Ra2+-compound dissolution by lactic acid (LA) solution, e.g., reactive organic carbon (i.e., electron-donor source), have been investigated, and optimum chemical conditions have been determined. The obtained data were also employed to predict the leaching kinetics and mechanism of the Ra2+-isotopes removal by three shrinking core models (SCM, liquid film process-chemical controlled process-diffusion controlled process) and Arrhenius model. The maximum leaching percentage of Ra2+-isotopes reached to 55-60% at the optimal leaching conditions (0.3 M LA, 5 h, 25 degrees C,phi< 1 mm, S/L ratio 10/50 g mL(-1)). The Ra-isotopes removal proceeds kinetically by diffusion-controlled process. Activation energy (E-a) of the leaching process was 10.51 kJ mol(-1). This value conforms that the leaching process for removal of Ra2+-isotopes in the TENORM scale waste by LA solution is controlled by a diffusion process. Values of thermodynamic parameters ( increment G(o), increment H-o, increment S-o) were determined and indicate that dissolution of Ra2+-isotopes in the studied waste is non-spontaneous and temperature dependent. Moreover, the leaching mechanism may be attributed to the dissolution of soluble exchangeable and acidic species of Ra2+-species and/or these due conversions of insoluble Ra-sulfate to more soluble Ra-sulfide and/or Ra-hydrogen sulfide by LA solutions.
机译:本研究以探索溶解如由沉积在油田管道和设备用于镭同位素(RA-228中,Ra-226,和(224)Ra)为在TENORM规模废物的动力学机制推断,苏伊士的海湾,埃及。主效率因子Ra2的+乳酸(LA)溶液,例如,反应性有机碳(即,电子给体源) - 化合物溶解,已经研究和最佳的化学条件已被确定。所获得的数据也采用由三个收缩核模型(SCM,液膜过程化学控制的过程扩散控制的过程)和阿仑尼乌斯模型来预测浸出动力学和Ra2的+ -isotopes去除机构。最大浸出Ra2的+的百分比-isotopes达到55-60%在最佳浸出条件(0.3M LA,5小时,25℃,披<1mm时,S / L比10/50克毫升(-1)) 。对RA-同位素去除由扩散控制的动力学过程进行。浸出过程的活化能(E-a)在10.51千焦耳摩尔(-1)。这个值符合该用于去除Ra2的+的浸出过程中通过LA溶液TENORM规模废物-isotopes通过扩散过程控制。热力学参数(增量G(○),增量H-O,增量S-O)的值进行了测定,并指示Ra2的+ -isotopes的在所研究的废物的溶解是不自然的和依赖于温度的。此外,浸出机制可以归因于Ra2的+ -species和/或通过LA中不溶镭硫酸盐的这些由于转换到更可溶镭硫化物和/或硫化物镭氢的可溶性可交换和酸性物质的溶解。

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