Valorization of waste eggshell for CO2 sorbents production by sol-gel citric acid treatment in a fixed-bed reactor

碳化作用 吸附 柠檬酸 蛋壳 原材料 化学工程 化学 解吸 材料科学 核化学 色谱法 有机化学 生态学 生物 工程类
作者
Cui Quan,María Cortazar,Laura Santamaria,Gartzen López,Chunfei Wu,Ningbo Gao
出处
期刊:Journal of CO2 utilization [Elsevier BV]
卷期号:75: 102562-102562 被引量:11
标识
DOI:10.1016/j.jcou.2023.102562
摘要

This study assesses the potential of the eggshells as a promising and alternative CO2 adsorbent. With the aim of enhancing the CO2 capture performance of raw eggshell, it was modified by sol-gel citric acid treatment. Both adsorbents were characterized by N2 adsorption-desorption, XRF, XRD and SEM techniques. Preliminary adsorption tests in TGA revealed that the acid-modified eggshell achieved significantly higher carbonation conversion than the raw eggshell adsorbent in the 650–750 ºC adsorption temperature range, reaching a carbonation conversion of 69% at 700 ºC. The cyclic performance of the modified eggshell, tested in TGA at 700 ºC under 15 vol% CO2, confirmed that sol-gel acid treatment led to a very stable adsorbent, with a slight improvement in CO2 adsorption capacity during the first four cycles (from 0.54 to 0.58 gCO2 gads−1), followed by stable performance due to self-reactivation phenomena. Moreover, additional experiments were carried out in a fixed bed reactor under more realistic conditions to study the influence of temperature (600–750 ºC) and CO2 flow rate (50–125 mL min−1) using the modified eggshell. An increase in temperature under 15 vol% CO2 stream led to a decrease in the carbonation conversion of the adsorbent, with the maximum CO2 uptake at 600 ºC (0.64 gCO2 gads−1). Regarding the role of the CO2 flow rate at 700 ºC, increasing from 75 to 125 mL min−1 CO2 had minimal effect, maintaining a capture amount of approximately 0.49 gCO2 gads−1. These results confirmed the potential of the acid-modified eggshell as a low-cost and environmental friendly adsorbent for CO2 capture, which indeed may significantly improve the economic feasibility of the CCUS processes.
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