Li Ruotong, Hu Xixuan, Huang Liang, Musyoka Nicholas Mulei, Xue Tianshan, Wang Qiang
Engineering Research Center for Water Pollution Source Control & Eco-Remediation, College of Environmental Science and Engineering, Beijing Forestry University, Beijing 100083, China.
State Key Laboratory of Efficient Production of Forest Resources, Beijing Forestry University, Beijing 100083, China.
Molecules. 2024 Mar 7;29(6):1192. doi: 10.3390/molecules29061192.
The dynamic adsorption characteristics of KCO-promoted layered double hydroxides (LDHs)-based adsorbent, with organic and inorganic anion intercalation, were studied. MgAl-LDH, KCO/MgAl-LDH, and KCO/MgAl-LDH(C16) with varying KCO loads were prepared and used for intermediate-temperature CO sequestration. The adsorbent was thoroughly characterized using X-ray diffraction, Brunauer-Emmett-Teller, scanning electron microscopy, and Fourier Transform Infrared Spectroscopy techniques, which revealed enhanced adsorption properties of MgAl-LDH, due to KCO promotion. Thermogravimetric CO adsorption tests on the constructed adsorbent materials showed that the 12.5 wt% KCO/MgAl-LDH(C16) adsorbent with organic anion intercalation exhibited optimal adsorption activity, achieving an adsorption capacity of 1.12 mmol/g at 100% CO and 350 °C. However, fixed-bed dynamic adsorption tests yielded different results; the 25 wt% KCO/MgAl-LDH prepared through inorganic anion intercalation exhibited the best adsorption performance in low-concentration CO penetration tests. The recorded penetration time was 93.1 s, accompanied by an adsorption capacity of 0.722 mmol/g. This can be attributed to the faster adsorption kinetics exhibited by the 25 wt% KCO/MgAl-LDH adsorbent during the early stages of adsorption, thereby facilitating efficient CO capture in low-concentration CO streams. This is a conclusion that differs from previous reports. Earlier reports indicated that LDHs with organic anion intercalation exhibited higher CO adsorption activity in thermogravimetric analyzer tests. However, this study found that for the fixed-bed dynamic adsorption process, KCO-modified inorganic anion-intercalated LDHs perform better, indicating their greater potential in practical applications.
研究了碳酸钾促进的层状双氢氧化物(LDHs)基吸附剂在有机和无机阴离子插层情况下的动态吸附特性。制备了不同碳酸钾负载量的MgAl-LDH、KCO/MgAl-LDH和KCO/MgAl-LDH(C16),并用于中温CO封存。使用X射线衍射、布鲁诺尔-埃米特-泰勒法、扫描电子显微镜和傅里叶变换红外光谱技术对吸附剂进行了全面表征,结果表明由于碳酸钾的促进作用,MgAl-LDH的吸附性能得到了增强。对构建的吸附剂材料进行的热重CO吸附测试表明,具有有机阴离子插层的12.5 wt% KCO/MgAl-LDH(C16)吸附剂表现出最佳吸附活性,在100% CO和350 °C下吸附容量达到1.12 mmol/g。然而,固定床动态吸附测试得出了不同的结果;通过无机阴离子插层制备的25 wt% KCO/MgAl-LDH在低浓度CO穿透测试中表现出最佳吸附性能。记录的穿透时间为93.1 s,吸附容量为0.722 mmol/g。这可归因于25 wt% KCO/MgAl-LDH吸附剂在吸附早期表现出更快的吸附动力学,从而有助于在低浓度CO气流中高效捕获CO。这一结论与先前的报道不同。早期报道表明,在热重分析仪测试中,具有有机阴离子插层的LDHs表现出更高的CO吸附活性。然而,本研究发现,对于固定床动态吸附过程,碳酸钾改性的无机阴离子插层LDHs表现更好,表明它们在实际应用中具有更大的潜力。