Green Chemistry in Red Emulsion: Interface of Dye Stabilized Emulsions as a Powerful Platform for the Formation of sub-20-nm SiO2 Nanoparticles
Source abstract
Abstract
Dye stabilized nanoemulsions offer the unique possibility of creating both silica capsules and sub-20-nm particles with precise control of particle size and narrow dispersity from the same system by the choice of the proper dye. The large o/w interface enhances the kinetics of particle formation significantly over macroscopic interfaces which enables the synthesis of silica nanoparticles without any catalyst or elevated temperatures under static conditions. This is in contrast to syntheses for sub-20-nm silica nanoparticles described until now which can normally not be conducted at neutral pH and/or room temperature without stirring. Furthermore, the synthesis can be run without any additional organic solvent and the dyes can be easily removed from the dispersion which opens the pathway to silica dispersions containing only particles, traces of ethanol and water at neutral pH without centrifugation, washing, or redispersion in accordance with the idea of "green chemistry".
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Mesoporous Materials and Catalysis · TiO2 Photocatalysis and Solar Cells · Quantum Dots Synthesis And Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Organic Chemistry III-Macromolecular Chemistry and Organic Materials, University of Ulm, Albert-Einstein-Allee 11, 89081 Ulm, Germany
Inorganic Chemistry II, University of Ulm, Albert-Einstein-Allee 11, 89081 Ulm, Germany
Funding
Verband der Chemischen Industrie
References (26)
Show source-provided references
1. 10.1021/acs.langmuir.6b0416010.1021/acs.langmuir.6b04160 ↗
2. 10.1016/j.jcis.2017.08.00710.1016/j.jcis.2017.08.007 ↗
3. 10.1002/jctb.501008020510.1002/jctb.5010080205 ↗
4. 10.1016/j.jcis.2007.12.04410.1016/j.jcis.2007.12.044 ↗
5. 10.1021/ja065071y10.1021/ja065071y ↗
6. 10.1021/la702528510.1021/la7025285 ↗
7. 10.1039/C5CC06598D10.1039/C5CC06598D ↗
8. 10.1021/la701063v10.1021/la701063v ↗
9. 10.1016/0021-9797(68)90272-510.1016/0021-9797(68)90272-5 ↗
10. 10.1021/bm060560b10.1021/bm060560b ↗
11. 10.1002/adem.20100010810.1002/adem.201000108 ↗
12. 10.1016/j.apsusc.2017.05.12410.1016/j.apsusc.2017.05.124 ↗
13. 10.1016/j.jcis.2005.02.01910.1016/j.jcis.2005.02.019 ↗
14. 10.1039/c1cc14743a10.1039/c1cc14743a ↗
15. 10.1007/s10971-013-3175-610.1007/s10971-013-3175-6 ↗
16. 10.1021/acs.langmuir.7b0114010.1021/acs.langmuir.7b01140 ↗
17. 10.1021/la062428310.1021/la0624283 ↗
18. 10.1039/C5NR08224B10.1039/C5NR08224B ↗
19. 10.1046/j.1365-2818.2003.01236.x10.1046/j.1365-2818.2003.01236.x ↗
20. Brinker C. J. · 1990
21. 10.1016/j.colsurfa.2011.11.00910.1016/j.colsurfa.2011.11.009 ↗
22. Derjaguin B. · Acta Phys. Chem. URSS · 1941 · 14 · 30
23. Verwey E. J. W. · 1948
24. 10.1039/CT907910200110.1039/CT9079102001 ↗
25. 10.1021/ja01665a00210.1021/ja01665a002 ↗
26. Iler R. K. · 1979