...
首页> 外文期刊>Journal of Chemical and Engineering Data: the ACS Journal for Data >New Proposal in a Biorefinery Context: Recovery of Acetic and Formic Acids by Adsorption on Hydrotalcites
【24h】

New Proposal in a Biorefinery Context: Recovery of Acetic and Formic Acids by Adsorption on Hydrotalcites

机译:生物遗炼背景下的新提案:通过对水滑石的吸附来恢复醋酸和甲酸

获取原文
获取原文并翻译 | 示例

摘要

Acetic acid (AA) and formic acid (FA) are two of the major fermentation inhibitors found in hemicellulosic hydrolysates. Their removal, which is necessary for the use of hydrolysates as fermentation substrates, can be achieved by adsorption on hydrotalcites. This study aimed to assess the efficiency of hydrotalcites in removing AA and FA from aqueous solution. Kinetic, thermodynamic, and equilibrium experiments were conducted using hydrotalcites composed of 30, 63, or 70% MgO. Calcined hydrotalcites composed of 70 and 63% MgO (MG70c and MG63c) had the best kinetic performance, removing 97% of FA and 91% of AA. The adsorption process followed pseudo-first-order kinetics. The Boyd model showed that external mass transfer or a combination of intraparticle diffusion and external mass transfer controls the process. Adsorption equilibrium was evaluated at different temperatures (30, 40, 50, and 60 degrees C) using MG70c as an adsorbent. The Freundlich model provided the best fit to adsorption isotherms. Thermodynamic studies indicated that adsorption was spontaneous and endothermic in nature. The results confirmed the efficiency of MG70c in removing AA and FA from aqueous solution.
机译:乙酸(AA)和甲酸(FA)是半纤维素水解产物中发现的两个主要发酵抑制剂。它们的去除是使用水解产物作为发酵基材的必需品,可以通过对水滑石的吸附来实现。本研究旨在评估水滑石术中除去水溶液中的AA和Fa的效率。使用由30,63或70%MgO组成的水滑石进行动力学,热力学和平衡实验。由70和63%MgO(MG70C和MG63C)组成的煅烧水滑石具有最佳的动力学性能,除去97%的FA和91%的AA。吸附过程遵循伪一阶动力学。 Boyd模型表明外部传质或粒地区扩散和外部传质的组合控制了该过程。使用Mg70C作为吸附剂在不同温度(30,40,50和60℃)的不同温度(30,40,50和60℃)中评价吸附平衡。 Freundlich模型提供了最适合吸附等温线。热力学研究表明,吸附是自发性和吸热的性质。结果证实了MG70C从水溶液中除去AA和Fa的效率。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号