Iron Gall Ink Revisited: In Situ Oxidation of Fe(II)–Tannin Complex for Fluidic‐Interface Engineering
Source abstract
Abstract
Abstract The ancient wisdom found in iron gall ink guides this work to a simple but advanced solution to the molecular engineering of fluidic interfaces. The Fe(II)–tannin coordination complex, a precursor of the iron gall ink, transforms into interface‐active Fe(III)–tannin species, by oxygen molecules, which form a self‐assembled layer at the fluidic interface spontaneously but still controllably. Kinetic studies show that the oxidation rate is directed by the counteranion of Fe(II) precursor salts, and FeCl2 is found to be more effective than FeSO4—an ingredient of iron gall ink—in the interfacial‐film fabrication. The optimized protocol leads to the formation of micrometer‐thick, free‐standing films at the air–water interface by continuously generating Fe(III)–tannic acid complexes in situ. The durable films formed are transferable, self‐healable, pliable, and postfunctionalizable, and are hardened further by transfer to the basic buffer. This O2‐instructed film formation can be applied to other fluidic interfaces that have high O2 level, demonstrated by emulsion stabilization and concurrent capsule formation at the oil–water interface with no aid of surfactants. The system, inspired by the iron gall ink, provides new vistas on interface engineering and related materials science.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Pickering emulsions and particle stabilization · Surfactants and Colloidal Systems · Enhanced Oil Recovery Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Center for Cell‐Encapsulation Research Department of Chemistry KAIST Daejeon 34141 Korea
Department of Mechanical Engineering KAIST Daejeon 34141 Korea
Department of Chemistry CICECO—Aveiro Institute of Materials University of Aveiro 3810‐193 Aveiro Portugal
Funding
National Research Foundation of Korea · H2020 European Research Council
References (78)
Show source-provided references
1. Zerdoun Bat‐Yehouda M. · 1983 · 96
2. 10.1021/acs.analchem.6b0008810.1021/acs.analchem.6b00088 ↗
3. 10.1039/c0dt00752h10.1039/c0dt00752h ↗
4. 10.1021/ic702272710.1021/ic7022727 ↗
5. McGavin G. · 2007
6. Krekel C. · Int. J. Forensic Doc. Exam. · 1999 · 5 · 54
7. 10.1016/j.corsci.2003.09.02110.1016/j.corsci.2003.09.021 ↗
8. 10.1016/S0010-938X(99)00137-710.1016/S0010-938X(99)00137-7 ↗
9. 10.1038/s41598-017-07257-x10.1038/s41598-017-07257-x ↗
10. 10.1006/abio.1997.252210.1006/abio.1997.2522 ↗
11. 10.1016/0006-2952(96)00101-310.1016/0006-2952(96)00101-3 ↗
12. 10.1016/j.nantod.2016.12.01210.1016/j.nantod.2016.12.012 ↗
13. 10.1002/asia.20130129110.1002/asia.201301291 ↗
14. 10.1126/science.123726510.1126/science.1237265 ↗
15. 10.1038/nnano.2016.17210.1038/nnano.2016.172 ↗
16. 10.1021/cm403903m10.1021/cm403903m ↗
17. 10.1002/smll.20180205210.1002/smll.201802052 ↗
18. 10.1021/acsami.8b0118910.1021/acsami.8b01189 ↗
19. 10.1002/cssc.20160161510.1002/cssc.201601615 ↗
20. 10.1039/C4NR07510B10.1039/C4NR07510B ↗
21. 10.1002/anie.20130492210.1002/anie.201304922 ↗
22. 10.1039/C6NR04469G10.1039/C6NR04469G ↗
23. 10.1002/adma.20170078410.1002/adma.201700784 ↗
24. 10.3390/polym904014010.3390/polym9040140 ↗
25. 10.1039/C5NR05573C10.1039/C5NR05573C ↗
26. 10.1002/adfm.20150003910.1002/adfm.201500039 ↗
27. 10.1002/anie.20140590510.1002/anie.201405905 ↗
28. 10.1021/acs.biomac.7b0124910.1021/acs.biomac.7b01249 ↗
29. 10.1021/acsomega.7b0106710.1021/acsomega.7b01067 ↗
30. 10.1002/adma.20170606310.1002/adma.201706063 ↗
31. 10.1021/acs.accounts.6b0042910.1021/acs.accounts.6b00429 ↗
32. 10.1021/acsnano.5b0270210.1021/acsnano.5b02702 ↗
33. 10.1038/nchem.102610.1038/nchem.1026 ↗
34. 10.1002/adma.20160671710.1002/adma.201606717 ↗
35. 10.1021/acs.chemmater.7b0334910.1021/acs.chemmater.7b03349 ↗
36. 10.1021/acs.langmuir.7b0269210.1021/acs.langmuir.7b02692 ↗
37. Park T. · Langmuir · 2018
38. 10.1002/chem.20150338010.1002/chem.201503380 ↗
39. 10.1021/bm301844u10.1021/bm301844u ↗
40. 10.1073/pnas.101586210810.1073/pnas.1015862108 ↗
41. 10.1039/C4TB01503G10.1039/C4TB01503G ↗
42. 10.1021/acs.chemmater.8b0261610.1021/acs.chemmater.8b02616 ↗
43. 10.1002/adma.20160329010.1002/adma.201603290 ↗
44. 10.1002/adma.20140325910.1002/adma.201403259 ↗
45. 10.1002/cnma.20160004710.1002/cnma.201600047 ↗
46. 10.1002/asia.20160014510.1002/asia.201600145 ↗
47. 10.1021/cr400531v10.1021/cr400531v ↗
48. 10.1021/ja057396510.1021/ja0573965 ↗
49. 10.1002/asia.20140299310.1002/asia.201402993 ↗
50. 10.1039/C5SC01225B10.1039/C5SC01225B ↗
51. Ruiz‐Molina D. · Angew. Chem., Int. Ed. · 2018
52. 10.1038/s41467-017-02387-210.1038/s41467-017-02387-2 ↗
53. Busque F. · 2015 · 277
54. 10.1021/acsami.5b0130410.1021/acsami.5b01304 ↗
55. 10.1002/adma.20120234310.1002/adma.201202343 ↗
56. 10.1039/c1cs15026j10.1039/c1cs15026j ↗
57. 10.1038/ncomms352010.1038/ncomms3520 ↗
58. 10.1021/acs.chemrev.6b0031410.1021/acs.chemrev.6b00314 ↗
59. 10.1002/anie.20160851510.1002/anie.201608515 ↗
60. 10.1021/bm06078210.1021/bm060782 ↗
61. 10.1063/1.55568010.1063/1.555680 ↗
62. 10.1021/acs.chemmater.5b0284710.1021/acs.chemmater.5b02847 ↗
63. 10.1016/0147-6513(90)90052-710.1016/0147-6513(90)90052-7 ↗
64. 10.1002/smll.20180234210.1002/smll.201802342 ↗
65. 10.1002/adma.20150474010.1002/adma.201504740 ↗
66. 10.1016/j.eurpolymj.2015.07.05310.1016/j.eurpolymj.2015.07.053 ↗
67. 10.1002/adhm.20130060310.1002/adhm.201300603 ↗
68. 10.1038/nchem.261710.1038/nchem.2617 ↗
69. 10.1002/smll.20170046710.1002/smll.201700467 ↗
70. 10.1039/C1CS15211D10.1039/C1CS15211D ↗
71. 10.1002/anie.20160923110.1002/anie.201609231 ↗
72. 10.1002/adhm.20140065710.1002/adhm.201400657 ↗
73. 10.1039/C4SM01813C10.1039/C4SM01813C ↗
74. 10.1021/ma047629x10.1021/ma047629x ↗
75. 10.1021/acs.accounts.6b0008710.1021/acs.accounts.6b00087 ↗
76. 10.1002/adfm.20130003810.1002/adfm.201300038 ↗
77. 10.1039/c2cs15264a10.1039/c2cs15264a ↗
78. 10.1021/nn301776y10.1021/nn301776y ↗