首页> 外文期刊>Radiochimica Acta: International Journal for Chemical Aspects of Nuclear Science and Technology >Preparation, characterization, uranium (VI) biosorption models, and conditions optimization by response surface methodology (RSM) for amidoxime-functionalized marine fungus materials
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Preparation, characterization, uranium (VI) biosorption models, and conditions optimization by response surface methodology (RSM) for amidoxime-functionalized marine fungus materials

机译:用响应表面方法(RSM)制备,表征,铀(VI)生物吸附模型及其对偕胺肟官能化的海洋真菌材料的优化

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摘要

Amidoxime-functionalized marine fungus Fusarium sp. #ZZF51 (ZGDA) was synthesized and studied to adsorb uranium (VI) from the aqueous solution. Different instrumental techniques such as FTIR, SEM, and TGA were employed for the characterization of the manufactured materials, and theirs ability of removal uranium (VI) was optimized using RSM. The experimental results showed the maximum adsorption capacity for the synthesized materials was 230.78 mg g(-1) at the following optimization conditions: S-L ratio 150 mg L-1, pH 5.13, uranium (VI) initial concentration 40 mg L-1, and equilibrium time 122.40 min. More than 85% of the absorbed uranium (VI) could be desorbed by 0.5 or 1.0 mol L-1 HCl, and the modified mycelium could be reused at least five times. The thermodynamic experimental data of adsorption uranium (VI) could fit better with Langumir and Freundlich isotherms models, and the pseudo-second-order model was better to interpret the kinetics process. The modified fungus materials exhibited the better sorption capacity for uranium (VI) in comparison with raw biomass should be attributed to the strong chelation of amidoxime to uranium (VI) ions.
机译:偕胺肟官能化海洋真菌镰刀菌。 #ZZF51(ZGDA)被合成并研究来自水溶液的吸附铀(VI)。采用不同的仪器技术,例如FTIR,SEM和TGA,用于制造材料的表征,使用RSM优化其去除铀(VI)的能力。实验结果表明,合成材料的最大吸附能力为230.78mg g(-1)在以下优化条件下:SL比150mg L-1,pH 5.13,铀(VI)初始浓度40mg L-1,和均衡时间122.40分钟。超过85%的吸收铀(VI)可以解吸0.5或1.0mol L-1 HCl,并且改性的菌丝体可以至少重复使用5次。吸附铀(VI)的热力学实验数据可以使用Langumir和Freundlich等温线模型更好地适合,并且伪二阶模型更好地解释动力学过程。与原料生物量相比,改性的真菌材料表现出铀(VI)的更好吸附能力,应归因于酰胺肟至铀(VI)离子的强烈螯合。

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