椰壳蒸汽活性炭和绿碱活性炭的制备与表征

Damilola Tosin Ojo , Omotayo Sarafadeen Amuda , Kazeem Kolapo Salam , Olarike Favour Oyediran , Basirat Bayonle Yekini
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引用次数: 0

摘要

本研究采用正在进行的绿色方法,从天然、环保的材料中开发活性炭,为商业产品提供可持续的替代品。采用绿色合成生产路线可以缓解活化过程中KOH持续排放所带来的环境问题。本研究提出了从可可豆荚壳中提取碱(CPHs)作为毒性较低的商业KOH的替代品。将提取的碱进一步用于活性炭的活化,制备新型椰壳碱活性炭。同时,采用蒸汽活化技术在不锈钢反应器中制备椰壳蒸汽活性炭(CSSA),流速为120 mL/h,温度为800°C,反应时间为5 h。利用傅里叶变换红外(FTIR)对椰壳活化样品(CSAA和CSSA)表面官能团进行了表征。利用扫描电子显微镜-能量色散x射线(SEM-EDX)研究了它们的表面形貌和元素组成。采用x射线衍射分析(XRD)进行了结构分析,采用布鲁诺尔-埃米特-泰勒(BET)方法检测了它们的比表面积和孔隙体积。100 g预处理前驱体在活化前的碳收率估计为89.25 %。用滴定法测定提取碱的浓度。提取碱的pH值为11.6,表明其为碱性,加入甲基橙指示剂后,溶液的颜色变为黄色。EDX结果证实,提取物主要由金属和钾组成,最高值为53.60 %wt。活性炭的FTIR结果显示-OH, C-H和C-O, CO官能团的存在表明炭化和活化成功进行。观察到的CSAA的附加峰可归因于K-O键的存在。两种活性炭均具有较大的BET比表面积,CSSA为1200.20 m²/g, CSAA为1250.20 m²/g。这些大的表面积总是使它们成为废水修复,水净化和气体捕获的合适吸附剂。新型CSAA的pHZC高达8.0,也证实了表面碱性官能团的存在,这可归因于碱活化的成功。基于这些分析结果,采用绿色萃取碱活化碳是一种安全的替代化学活化剂的使用。从提取到活化的整个过程是清洁的,不会向环境释放任何有毒物质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation and characterization of steam-activated and green alkali-activated carbon from coconut shells
This study adopts the ongoing green approach to develop activated carbon from natural, eco-friendly materials offering a sustainable alternative to commercially available products. The environmental problem that arises from consistent discharge of KOH during activation can be alleviated by adopting the green synthetic route of production. This study presents the extraction of alkali from cocoa pod husks (CPHs) as less harmful alternative to toxic commercial KOH. The extracted alkali was further utilized in activation of carbon to produce novel coconut shell alkali activated carbon (CSAA). Simultaneously, coconut shell steam activated carbon (CSSA) was prepared using steam activation technique in a stainless-steel reactor at a flow rate of 120 mL/hour at 800° °C for 5 h. Both coconut shell based activated samples (CSAA and CSSA) were characterized using Fourier Transform Infrared (FTIR) analysis for surface functional groups identification. Their surface morphologies and elemental composition were investigated using Scanning Electron Microscopy-Energy Dispersive X-ray (SEM-EDX). X-ray Diffraction analysis (XRD) were employed for textural analysis while Brunauer-Emmett-Teller (BET) methods examined their specific surface areas as well as pore volumes. The yield of carbon from 100 g of pre-treated precursor was estimated as 89.25 % before activation. The concentration of the extracted alkali was evaluated using the titration technique. The pH of 11.6 obtained for extracted alkali suggests alkalinity which was confirmed by observable colour change of solution to yellow on the addition of drops of methyl orange indicator. The EDX result confirms that extract is composed primarily of metals with potassium having the highest value of 53.60 %wt. The FTIR results of the activated carbons showed the presence of -OH, C-H, and C-O, CO functional groups suggesting carbonization and activation was successfully conducted. Additional peaks observed for CSAA can be attributed to the presence of K-O bonds. Both activated carbons are characterized by large BET surface areas of 1200.20 m²/g for CSSA and 1250.20 m²/g for CSAA. These large surface areas invariably make them suitable adsorbents for wastewater remediation, water purification, and trapping of gases. The higher pHZC of 8.0 obtained for novel CSAA also confirms the presence of surface basic functional groups which can be attributed to successful alkali activation. Based on these analytical findings, adoption of green extracted alkali in activation of carbon is a safe alternative to the use of chemical activators. The entire procedure from extraction to activation is clean without the release of any toxic substances to the environment.
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