Co-intercalation of Acid Red 337 and a UV Absorbent into Layered Double Hydroxides: Enhancement of Photostability
Source abstract
Abstract
Organic-inorganic hybrid pigments with enhanced thermo- and photostability have been prepared by co-intercalating C.I. Acid Red 337 (AR337) and a UV absorbent (BP-4) into the interlayer of ZnAl layered double hydroxides through a coprecipitation method. The obtained compounds were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric-differential thermogravimetric-differential thermal analysis, UV-visible spectroscopy, and the International Commission on Illumination (CIE) 1976 L*a*b* color scales. The results show the successful co-intercalation of AR337 and BP-4 into the interlayer region of layered double hydroxides (LDHs) and reveal the presence of host-guest interactions between LDH host layers and guest anions of AR337 and BP-4 and guest-guest interactions between AR337 and BP-4. The intercalation can improve the thermostability of AR337 due to the protection of LDH layers. Moreover, the co-intercalation of AR337 and BP-4 not only markedly enhances the photostability of AR337 but also significantly influences the color of the hybrid pigment.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Layered Double Hydroxides Synthesis and Applications · Advanced Photocatalysis Techniques · Polyoxometalates: Synthesis and Applications
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, People’s Republic of China
Funding
National Natural Science Foundation of China · Fundamental Research Funds for the Central Universities · State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology
References (38)
Show source-provided references
1. Jesionowski T. · Dyes Pigm. · 2011 · 89 · 12710.1016/j.dyepig.2010.09.014 ↗
2. Cao L. · Ind. Eng. Chem. Res. · 2014 · 53 · 3110.1021/ie4021914 ↗
3. Thetford D. · Dyes Pigm. · 2003 · 59 · 18510.1016/S0143-7208(03)00104-9 ↗
4. Sanchez C. · Chem. Soc. Rev. · 2011 · 40 · 69610.1039/c0cs00136h ↗
5. Williams G. R. · J. Mater. Chem. · 2006 · 16 · 306510.1039/b604895a ↗
6. Wang Q. · Chem. Rev. · 2012 · 112 · 412410.1021/cr200434v ↗
7. Feng Y. · Ind. Eng. Chem. Res. · 2014 · 53 · 228710.1021/ie403643v ↗
8. Yan D. · Angew. Chem., Int. Ed. · 2011 · 50 · 703710.1002/anie.201102232 ↗
9. Crites C. O. L. · ACS Catal. · 2013 · 3 · 206210.1021/cs400337w ↗
10. Cho S. · Adv. Funct. Mater. · 2013 · 23 · 234810.1002/adfm.201201883 ↗
11. Gong M. · J. Am. Chem. Soc. · 2013 · 135 · 845210.1021/ja4027715 ↗
12. Choi S. J. · Nanomedicine · 2011 · 6 · 80310.2217/nnm.11.86 ↗
13. Park D. H. · Prog. Polym. Sci. · 2013 · 38 · 144210.1016/j.progpolymsci.2013.05.007 ↗
14. Othman M. A. · J. Hazard. Mater. · 2013 · 254 · 22110.1016/j.jhazmat.2013.03.030 ↗
15. Theiss F. L. · J. Colloid Interface Sci. · 2014 · 417 · 35610.1016/j.jcis.2013.11.040 ↗
16. Wen T. · ACS Appl. Mater. Interfaces · 2013 · 5 · 330410.1021/am4003556 ↗
17. Liang J. · Chem. Mater. · 2010 · 22 · 37110.1021/cm902787u ↗
18. Chen L. · Nanoscale · 2013 · 5 · 1098210.1039/c3nr03031h ↗
19. Shi W. · Adv. Funct. Mater. · 2010 · 20 · 385610.1002/adfm.201001081 ↗
20. Leroux F. · J. Mater. Chem. · 2010 · 20 · 948410.1039/b926978a ↗
21. Kang N. J. · ACS Appl. Mater. Interfaces · 2013 · 5 · 899110.1021/am4020555 ↗
22. Coelho C. · RSC Adv. · 2012 · 2 · 543010.1039/c2ra20579c ↗
23. Latterini L. · Inorg. Chim. Acta · 2007 · 360 · 72810.1016/j.ica.2006.07.048 ↗
24. Tang P. · Dyes Pigm. · 2014 · 104 · 13110.1016/j.dyepig.2013.12.012 ↗
25. Bauer J. · Adv. Funct. Mater. · 2003 · 13 · 24110.1002/adfm.200390036 ↗
26. Chakraborty C. · J. Phys. Chem. C · 2010 · 115 · 199610.1021/jp110486r ↗
27. Marangoni R. · J. Colloid Interface Sci. · 2009 · 333 · 12010.1016/j.jcis.2009.02.001 ↗
28. Marangoni R. · J. Colloid Interface Sci. · 2008 · 326 · 36610.1016/j.jcis.2008.06.030 ↗
29. Tang P. · Ind. Eng. Chem. Res. · 2012 · 51 · 1054210.1021/ie300645b ↗
30. Guo X. · Langmuir · 2009 · 25 · 989410.1021/la901012w ↗
31. Mandal S. · Langmuir · 2009 · 25 · 1098010.1021/la901201s ↗
32. Zhang J. · J. Colloid Interface Sci. · 2013 · 411 · 24010.1016/j.jcis.2013.08.008 ↗
33. Chen C. · Nanoscale · 2013 · 5 · 431410.1039/c3nr00781b ↗
34. Sun Z. · Chem. Eng. J. · 2010 · 161 · 29310.1016/j.cej.2010.04.031 ↗
35. Wang H. · AlChE J. · 2010 · 56 · 76810.1002/aic.12020 ↗
36. Hirano Y. · Langmuir · 2007 · 23 · 700310.1021/la700254p ↗
37. Berlepsch H. v. · Phys. Chem. Chem. Phys. · 2014 · 16 · 1065910.1039/C4CP00967C ↗
38. Kinashi K. · Dyes Pigm. · 2012 · 92 · 78310.1016/j.dyepig.2011.05.024 ↗