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Catalytic degradation of tetracycline hydrochloride by persulfate activated with nano Fe-0 immobilized mesoporous carbon

机译:用纳米Fe-0固定化的介孔碳,过硫酸盐催化降解盐酸四环素盐酸盐

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In this study, mesoporous carbon (MC) supported nano Fe-0 was prepared from polyvinyl alcohol (PVA) using MnCO3 as template, which was used as the catalyst to activate persulfate (PS) for the removal of tetracycline hydrochloride (TC) from aqueous solution. The nano Fe-0 was immobilized on MC by liquid phase reduction to overcome the drawbacks of nano Fe-0 for persulfate (PS) activation, including being easily aggregated and oxidized. The experimental results showed that the nano Fe-0/MC + PS system achieved 92.1% of TC removal, while the MC + PS system and nano Fe-0 + PS systems showed 78.5% and 33.7% of TC removal, respectively. High removal efficiency in the nano Fe-0/MC + PS system could be attributed to the superior PS activation capability due to the synergistic effects of nano Fe-0 and MC. In order to better understand the removal mechanism, the effects of nano Fe-0 loading amount (c), dosage (m), PS/TC mole ratio (R-m) and initial pH on TC removal were evaluated in the nano Fe-0/MC + PS system. The results showed that the removal efficiency of TC was enhanced with the increase of nano Fe-0 loading amount and dosage, while slightly decrease with the increase of PS/TC mole ratio. The maximum removal of TC was 97.7% under the optimal conditions: c = 20%, m = 0.8 g/L, = 50/1 and pH = 5. According to the results of radical scavengers' studies and intermediates analysis, SO4 center dot-, which was produced from catalytic activation of PS by nano Fe-0 and Fe2+ on the surface of Fe-0/MC, plays a significant role for TC degradation in the nano Fe-0/MC + PS system. The Fe-0/MC + PS system exhibited a superior oxidation process for the removal of TC from aqueous solution with excellent stability and reusability of Fe-0/MC.
机译:在该研究中,使用MnCo3作为模板由聚乙烯醇(PVA)制备介孔碳(MC)负载的纳米Fe-0,用作催化剂以激活过硫酸盐(PS)以从含水水溶液去除四环素盐酸盐(TC)解决方案。通过液相减少将纳米Fe-0固定在MC上,以克服纳米Fe-0的缺点对于过硫酸盐(PS)活化,包括容易聚集和氧化。实验结果表明,纳米Fe-0 / MC + PS系统达到了92.1%的TC去除,而MC + PS系统和纳米Fe-0 + PS系统分别显示出78.5%和33.7%的TC去除。由于纳米Fe-0和MC的协同效应,纳米Fe-0 / MC + PS系统中的高除去效率可归因于优异的PS激活能力。为了更好地了解去除机制,在纳米Fe-0 /中评价纳米Fe-0负载量(c),剂量(m),剂量(m),ps / tc摩尔比(Rm)和初始pH的初始pH的效果。 MC + PS系统。结果表明,随着纳米Fe-0加载量和剂量的增加,增强了Tc的去除效率,同时随着PS / TC摩尔比的增加而略微降低。在最佳条件下,Tc的最大去除为97.7%:C = 20%,m = 0.8g / L,= 50/1和pH = 5.根据激进清除剂的研究和中间体分析,SO4中心点的结果 - 从Fe-0 / MC的表面上通过纳米Fe-0和Fe 2 +从PS的催化活化产生的,在纳米Fe-0 / MC + PS系统中对TC降​​解起显着作用。 Fe-0 / MC + PS系统表现出优异的氧化方法,用于从水溶液中除去TC,具有优异的Fe-0 / MC的稳定性和可重用性。

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