Low-cost Rice Husk Ash and Silica for Chromium Ion Sorption from Aqueous System: Characterisation and Kinetics

Adelagun Ruth Olubukola Ajoke
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引用次数: 1

Abstract

Several materials have been developed and used to remove Chromate (VI) from industrial wastewater before discharge into the environment because of its toxicity and lethality. In this study, low-cost adsorbents (rice husk ash (RHA) and silica (RHS)) were prepared from rice husks purchased locally from a rice mill industry and characterised. While the crystallinity and mineralogy of the adsorbents were analysed using powdered XRD crystallography, analysis of the physico-chemical properties was performed using standard procedures. Elemental analysis (CHN) was done using Perkin Elmer CHN elemental analyser and FTIR Spectrometer was used to determine the functional groups on the surface of the adsorbents at room temperature. The prepared samples were used as adsorbents for the removal of chromate (VI) ion in a batch sorption process with reaction conditions vis–a-viz adsorbent dosage = 0.5 g, adsorbate volume = 500 ml, adsorbate solution concentrations: 10-200 mg/l, time = 4 h, temperature = ambient temperature. The residual Cr (VI) concentration in the solution was analyzed spectrophotometrically at λ = 540 nm following the 1,5–diphenylcarbazide procedure. Results obtained for the characterisation of the adsorbents were similar and comparable with what obtained in literatures. Physico - chemical analysis revealed a high ash content of 89% and silica content of 95.83%. XRD analysis for the rice husk ash samples reflected the presence of cristobalite (SiO2) in amorphous form and a characteristics broad peak at 2θ angle = 26.5°. FTIR analysis revealed the presence of silanol groups (Si-OH), silicic acid (Si-O-Si-OH) in the ash and Si-O-Si and Si-O) in the silica. The results of effect of time-concentration experiments of chromium ion sorption by the adsorbents revealed that Cr (VI) ion sorption was both time and initial solution concentration dependent with over 80% removal achieved within the first 30 min of contact for both adsorbents as the initial chromate concentration was increased. Kinetic modeling of the process showed up for pseudo second order, hinting on chemisorption as the mechanism of interaction.
低成本稻壳灰和二氧化硅对水系统中铬离子的吸附:表征和动力学
由于工业废水中铬酸盐(VI)具有毒性和致死率,人们开发了几种材料来去除工业废水中的铬酸盐(VI)。在这项研究中,低成本吸附剂(稻壳灰(RHA)和二氧化硅(RHS))是从当地购买的稻壳中制备的,并对其进行了表征。使用粉末XRD晶体学分析吸附剂的结晶度和矿物学,使用标准程序分析其物理化学性质。采用Perkin Elmer元素分析仪进行元素分析(CHN),并用FTIR光谱仪在室温下测定吸附剂表面的官能团。将制备的样品作为吸附剂,在吸附剂用量为0.5 g,吸附剂体积为500 ml,吸附剂溶液浓度为10-200 mg/l,时间为4 h,温度为环境温度的条件下,对铬酸盐(VI)离子进行了间歇吸附。采用1,5 -二苯脲法,在λ = 540 nm处分光光度法测定了溶液中残留Cr (VI)的浓度。所得到的吸附剂的表征结果与文献中所得到的相似和可比较。理化分析表明其灰分含量高达89%,二氧化硅含量高达95.83%。稻壳灰分样品的XRD分析反映出方石英(SiO2)以无定形存在,且在2θ角= 26.5°处有一个特征宽峰。FTIR分析显示灰分中存在硅醇基团(Si-OH)和硅酸(Si-O-Si-OH),二氧化硅中存在硅- o - si和硅- o。吸附材料对铬离子吸附的时间-浓度实验结果表明,Cr (VI)离子的吸附与时间和初始溶液浓度有关,随着初始铬酸盐浓度的增加,两种吸附剂在接触后30 min内的去除率均超过80%。该过程的动力学模型显示为准二级,暗示化学吸附是相互作用的机制。
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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