响应面优化棉秆基活性炭的制备及其吸附性能研究

宾齐, 李海红, 张田田

现代化工 ›› 2021, Vol. 41 ›› Issue (6) : 161 -166.

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现代化工 ›› 2021, Vol. 41 ›› Issue (6) : 161-166. DOI: 10.16606/j.cnki.issn0253-4320.2021.06.033
科研与开发

响应面优化棉秆基活性炭的制备及其吸附性能研究

    宾齐, 李海红, 张田田
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Optimization of cotton stalk-based activated carbon preparation by response surface and study on adsorption properties

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摘要

以棉花秸秆为原料、ZnCl2/AlCl3为改性剂制备活性炭(AC)。利用中心复合设计法(CCD)对主要影响因子进行参数优化,并利用预测模型确定最佳制备工艺为:活化温度为640℃、浸渍质量比(棉秸秆与改性剂的质量比)为1.58:1、活化时间为87 min、改性剂配比(改性剂中ZnCl2与AlCl3的质量比)为9:1。在实际实验条件下,样品得率、总酸含量分别为44.32%、0.87 mmol/g,与模型预测值误差分别为1.79%、1.04%。利用碱性有机染料甲基紫研究其吸附性能,当活性炭投加量为1.18 g/L、溶液质量浓度为82.00 mg/L时,其对甲基紫去除率均能达到90%以上。ZnCl2/AlCl3改性棉秸秆基活性炭具有良好的吸附性能,为棉秸秆的应用提供了参考依据。

Abstract

Activated carbon is prepared by chemical activation method using cotton stalk as material and ZnCl2/AlCl3 as modifier.Central Composite Design (CCD) method is used to optimize the parameters of main influencing factors.By utilizing the predicted model,the optimum parameters are obtained as follows:activation temperature at 640℃,mass ratio between cotton straw and modifier is 1.58∶1,activation time lasts for 87 min,and mass ratio of ZnCl2 to AlCl3 in modifier is 9∶1.Under actual experimental conditions,the sample yield and total acid content are 44.32% and 0.87 mmol·g-1,respectively,and the errors to the predicted values are 1.79% and 1.04%,respectively.Structure and composition of the prepared activated carbon are characterized.The removal rate of methyl violet by the prepared activated carbon can exceed 90% when the dosage of activated carbon is 1.18 g·L-1 and the concentration of solution is 82.00 mg·L-1.ZnCl2/AlCl3 modified cotton stalk-based activated carbon has good adsorption properties,which provides references for the application of cotton stalks.

关键词

棉花秸秆 / 吸附性能 / 响应曲面 / 活性炭 / 改性

Key words

cotton straw / adsorptive property / response surface / activated carbon / modification

Author summay

宾齐(1995-),女,硕士研究生,研究方向为环保材料,1457636356@qq.com

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响应面优化棉秆基活性炭的制备及其吸附性能研究[J]. 现代化工, 2021, 41(6): 161-166 DOI:10.16606/j.cnki.issn0253-4320.2021.06.033

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