Adsorptive removal of Cr(VI) from aqueous solution using sulfuric acid-treated diatomite

IF 4.2 Q2 CHEMISTRY, MULTIDISCIPLINARY Results in Chemistry Pub Date : 2025-05-01 Epub Date: 2025-03-17 DOI:10.1016/j.rechem.2025.102205
Sintayehu Shewatatek , Girma Gonfa , Sintayehu Mekuria Hailegiorgis , Belete Tessema
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Abstract

In this study, diatomite underwent acid treatment and was examined for its capability to adsorb chromium (VI) (Cr (VI)) from water. The diatomite was treated with sulfuric acid (H₂SO₄) in varying concentrations (2–10 M) over different activation times (4–12 h), solid-to-liquid ratios (50–250 g/L), and activation temperatures (60–90). Optimal Cr (VI) removal was achieved with a 4 M H2SO4 concentration, an activation time of 10 h, a solid-to-liquid ratio of 50 g/L, and an activation temperature of 90 °C. Both raw diatomite and acid-treated diatomite (TDE) were characterized using scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FTIR), Brunauer, Emmett, and Teller (BET), and X-ray diffractometer (XRD). BET analysis showed an increase in surface area from 22.39 m2/g to 34.83 m2/g after treatment. The maximum Cr(VI) removal efficiency of 86.7 % was achieved at pH 2, 0.3 g/100 mL adsorbent dosage, 60 min contact time, and 10 ppm initial Cr(VI) concentration, according to the optimization of adsorption studies that were carried out across varying pH (2−10), adsorbent dosage (0.1–0.5 g/100 mL), contact time (15–75 min), and initial Cr(VI) concentration (10–30 ppm). The Freundlich and Sips isotherm models provided the best description of the adsorption process, revealing heterogeneous surface interactions and a maximum adsorption capacity of 16.395 mg/g. Chemisorption was confirmed as the major mechanism by kinetic analysis, which showed that the pseudo-second-order model fit the data the best. Thermodynamic studies validated the process as spontaneous and endothermic. These findings show that diatomite treated with sulfuric acid is a very efficient adsorbent for removing Cr(VI) from tainted water.

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硫酸处理硅藻土吸附去除水溶液中的铬(VI)
本研究对硅藻土进行酸处理,考察其对水中铬(Cr (VI))的吸附能力。用不同浓度(2-10 M)硫酸(H₂SO₄)在不同活化时间(4-12 H)、固液比(50-250 g/L)和活化温度(60-90)下处理硅藻土。当H2SO4浓度为4 M,活化时间为10 h,固液比为50 g/L,活化温度为90℃时,Cr (VI)去除率最佳。采用扫描电镜(SEM)、傅里叶变换红外光谱(FTIR)、Brunauer, Emmett, and Teller (BET)和x射线衍射仪(XRD)对原料硅藻土和酸处理硅藻土(TDE)进行了表征。BET分析显示,处理后的比表面积由22.39 m2/g增加到34.83 m2/g。在pH为2、吸附剂用量为0.3 g/100 mL、接触时间为60 min、初始Cr(VI)浓度为10 ppm的条件下,对Cr(VI)的最大去除率为86.7%,并对不同pH(2−10)、吸附剂用量(0.1 ~ 0.5 g/100 mL)、接触时间(15 ~ 75 min)和初始Cr(VI)浓度(10 ~ 30 ppm)进行了优化吸附研究。Freundlich和Sips等温线模型对吸附过程的描述最好,揭示了非均相表面相互作用,最大吸附量为16.395 mg/g。动力学分析证实了化学吸附是主要机理,拟二阶模型与实验数据拟合最好。热力学研究证实了这一过程是自发和吸热的。研究结果表明,硫酸处理硅藻土是一种非常有效的去除水中Cr(VI)的吸附剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Results in Chemistry
Results in Chemistry Chemistry-Chemistry (all)
CiteScore
2.70
自引率
8.70%
发文量
380
审稿时长
56 days
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