Super‐Stable Mineralization of Ni2+ Ions from Wastewater using CaFe Layered Double Hydroxide
Source abstract
Abstract
Abstract The dealing/recycling of Ni‐containing wastewater pollution has aroused great attention both from environmental science and resource utilization perspectives. Herein, a classic CaFe‐layered double hydroxide (CaFe‐LDH) stabilizer, which exhibits a super‐stable mineralization efficiency for removing Ni2+ ions with a maximum saturated removal capacity of 321 mg g−1 is prepared. This stabilizer can remove not only 10 000 mg L−1 Ni2+ ions to a few mg L−1, but also 1 mg L−1 Ni2+ ions to 2 µg L−1. Moreover, the CaFe‐LDH shows great mineralization capability for the real Ni‐containing electroplating solution. It is demonstrated by ex situ X‐ray diffraction and extended X‐ray absorption fine structure characterization that the isomorphous substitution of Ca2+ by Ni2+ in the laminate of LDH dominates the mineralization process, and the CaFe‐LDH is transformed to the corresponding NiCaFe‐LDH accordingly. Further application of the resultant NiCaFe‐LDH shows improved electrocatalytic oxygen evolution reaction and photocatalytic CO2 reduction activities. This work paves great way for Ni2+ ion removal from wastewater and utilization of the recycled Ni resource.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Layered Double Hydroxides Synthesis and Applications · Supercapacitor Materials and Fabrication · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing 100029 China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Beijing Municipality · Fundamental Research Funds for the Central Universities
References (50)
Show source-provided references
1. 10.1002/anie.20200587810.1002/anie.202005878 ↗
2. 10.1016/j.cej.2016.08.05410.1016/j.cej.2016.08.054 ↗
3. 10.1002/adfm.20200616810.1002/adfm.202006168 ↗
4. 10.1002/adfm.20180050210.1002/adfm.201800502 ↗
5. 10.1016/j.apcatb.2020.11957510.1016/j.apcatb.2020.119575 ↗
6. 10.1016/j.jcis.2017.02.05810.1016/j.jcis.2017.02.058 ↗
7. 10.1016/j.jhazmat.2019.01.09410.1016/j.jhazmat.2019.01.094 ↗
8. 10.1016/j.ccr.2021.21380910.1016/j.ccr.2021.213809 ↗
9. 10.1038/ngeo287610.1038/ngeo2876 ↗
10. 10.1021/cr200434v10.1021/cr200434v ↗
11. Li T. · Acta Phys.‐Chim. Sin. · 2020 · 36
12. 10.1016/j.cej.2016.06.00710.1016/j.cej.2016.06.007 ↗
13. 10.1016/j.cej.2020.12455410.1016/j.cej.2020.124554 ↗
14. 10.1016/j.clay.2020.10586710.1016/j.clay.2020.105867 ↗
15. 10.1021/jacs.7b0712310.1021/jacs.7b07123 ↗
16. 10.1021/jacs.6b0011010.1021/jacs.6b00110 ↗
17. 10.1016/j.cej.2020.12717810.1016/j.cej.2020.127178 ↗
18. 10.1021/cm980523u10.1021/cm980523u ↗
19. 10.1002/adfm.20190983210.1002/adfm.201909832 ↗
20. 10.1016/j.ultsonch.2019.02.02410.1016/j.ultsonch.2019.02.024 ↗
21. 10.1016/j.cej.2011.11.07410.1016/j.cej.2011.11.074 ↗
22. 10.1016/j.cej.2020.12592210.1016/j.cej.2020.125922 ↗
23. 10.1021/acssuschemeng.8b0342810.1021/acssuschemeng.8b03428 ↗
24. 10.1016/j.chemosphere.2020.12893710.1016/j.chemosphere.2020.128937 ↗
25. 10.1016/j.scitotenv.2020.14364010.1016/j.scitotenv.2020.143640 ↗
26. 10.1016/j.jhazmat.2019.12100010.1016/j.jhazmat.2019.121000 ↗
27. 10.1016/j.jhazmat.2017.06.01010.1016/j.jhazmat.2017.06.010 ↗
28. 10.1016/j.cej.2018.11.22510.1016/j.cej.2018.11.225 ↗
29. 10.1021/acsami.0c1184710.1021/acsami.0c11847 ↗
30. 10.1002/aenm.20170358510.1002/aenm.201703585 ↗
31. 10.1002/anie.20190424610.1002/anie.201904246 ↗
32. 10.1021/acscatal.7b0302210.1021/acscatal.7b03022 ↗
33. 10.1002/anie.20180968910.1002/anie.201809689 ↗
34. 10.1016/j.cej.2020.12836210.1016/j.cej.2020.128362 ↗
35. 10.1002/adma.20170536910.1002/adma.201705369 ↗
36. 10.1016/j.apcatb.2020.11888410.1016/j.apcatb.2020.118884 ↗
37. 10.1016/j.jechem.2020.04.06310.1016/j.jechem.2020.04.063 ↗
38. 10.1021/cr500008u10.1021/cr500008u ↗
39. 10.1002/smm2.100510.1002/smm2.1005 ↗
40. 10.1002/adma.20160645910.1002/adma.201606459 ↗
41. 10.1007/s12209-020-00265-510.1007/s12209-020-00265-5 ↗
42. 10.1007/s40820-020-00421-510.1007/s40820-020-00421-5 ↗
43. 10.1039/C8TA04721A10.1039/C8TA04721A ↗
44. Wang H.‐Y. · Acta Phys.‐Chim. Sin. · 2018 · 34 · 22
45. 10.1016/j.gee.2017.01.00110.1016/j.gee.2017.01.001 ↗
46. 10.1021/acscatal.8b0133210.1021/acscatal.8b01332 ↗
47. 10.1016/j.jechem.2018.09.01110.1016/j.jechem.2018.09.011 ↗
48. 10.1016/j.jelechem.2006.11.00810.1016/j.jelechem.2006.11.008 ↗
49. 10.1038/s41467-019-08697-x10.1038/s41467-019-08697-x ↗
50. 10.1016/j.xcrp.2021.10032210.1016/j.xcrp.2021.100322 ↗