Self-Healing Phase Change Salogels with Tunable Gelation Temperature
Source abstract
Abstract
Chemically cross-linked polymer matrices have demonstrated strong potential for shape stabilization of molten phase change materials (PCM). However, they are not designed to be fillable and removable from a heat exchange module for an easy replacement with new PCM matrices and lack self-healing capability. Here, a new category of shapeable, self-healing gels, "salogels", is introduced. The salogels reversibly disassemble in a high-salinity environment of a fluid inorganic PCM [lithium nitrate trihydrate (LNH)], at a preprogrammed temperature. LNH was employed as a high latent heat PCM and simultaneously as a solvent, which supported the formation of a network of polyvinyl alcohol (PVA) chains via physical cross-linking through poly(amidoamine) dendrimers of various generations. The existence of hydrogen bonding and the importance of low-hydration state of PVA for the efficient gelation were experimentally confirmed. The thermal behavior of PCM salogels was highly reversible and repeatable during multiple heating/cooling cycles. Importantly, the gel-sol transition temperature could be precisely controlled within a range of temperature above LNH's melting point by the choice of dendrimer generation and their concentration. Shape stabilization and self-healing properties of the salogels, taken together with tunability of their temperature-induced fluidization make these materials attractive for thermal energy storage applications that require on-demand removal and replacement of used inorganic PCM salt hydrates.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Polymer composites and self-healing · Aerogels and thermal insulation · Photochromic and Fluorescence Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, Texas A&M University, 3003 TAMU, 209 Reed McDonald, College Station, Texas 77843-3003, United States
Funding
Texas A and M Engineering Experiment Station, Texas A and M University
References (72)
Show source-provided references
1. 10.1016/s0079-6700(97)00047-610.1016/s0079-6700(97)00047-6 ↗
2. 10.1016/s1359-6446(02)02255-910.1016/s1359-6446(02)02255-9 ↗
3. 10.1039/c2cs35264h10.1039/c2cs35264h ↗
4. 10.1016/j.ajps.2013.07.00610.1016/j.ajps.2013.07.006 ↗
5. 10.1002/adma.20170169510.1002/adma.201701695 ↗
6. 10.1021/ma902219710.1021/ma9022197 ↗
7. 10.1039/c3cs60109a10.1039/c3cs60109a ↗
8. 10.1016/s0169-409x(97)00121-x10.1016/s0169-409x(97)00121-x ↗
9. 10.1021/ja060649p10.1021/ja060649p ↗
10. 10.1021/la061669810.1021/la0616698 ↗
11. 10.1002/marc.20080071310.1002/marc.200800713 ↗
12. 10.1038/nmat261410.1038/nmat2614 ↗
13. 10.1038/ncomms729510.1038/ncomms7295 ↗
14. 10.1021/cr000108x10.1021/cr000108x ↗
15. 10.1016/j.apenergy.2010.01.01010.1016/j.apenergy.2010.01.010 ↗
16. 10.1039/c6ta08850c10.1039/c6ta08850c ↗
17. 10.1002/aic.1595610.1002/aic.15956 ↗
18. 10.1016/j.enconman.2003.09.01510.1016/j.enconman.2003.09.015 ↗
19. 10.1021/acsami.7b0008610.1021/acsami.7b00086 ↗
20. 10.1039/c7ta02897k10.1039/c7ta02897k ↗
21. 10.1016/s1359-4311(02)00192-810.1016/s1359-4311(02)00192-8 ↗
22. 10.1002/adma.20090332810.1002/adma.200903328 ↗
23. 10.1021/je300046910.1021/je3000469 ↗
24. 10.1016/j.rser.2007.10.00510.1016/j.rser.2007.10.005 ↗
25. Hale D. V. · 1971
26. Hoover M. J. · 1971
27. 10.1039/c5ta00606f10.1039/c5ta00606f ↗
28. 10.1016/j.actamat.2014.10.05110.1016/j.actamat.2014.10.051 ↗
29. 10.1016/j.rser.2010.10.00610.1016/j.rser.2010.10.006 ↗
30. 10.1016/j.jcis.2015.02.02010.1016/j.jcis.2015.02.020 ↗
31. 10.1016/j.solener.2013.08.02110.1016/j.solener.2013.08.021 ↗
32. 10.1016/j.matchemphys.2010.03.04210.1016/j.matchemphys.2010.03.042 ↗
33. 10.1016/s0196-8904(01)00010-310.1016/s0196-8904(01)00010-3 ↗
34. 10.1016/j.apenergy.2016.10.02110.1016/j.apenergy.2016.10.021 ↗
35. 10.1002/zaac.1968357011210.1002/zaac.19683570112 ↗
36. 10.1295/polymj.17.11710.1295/polymj.17.117 ↗
37. 10.1071/ch1352510.1071/ch13525 ↗
38. 10.1021/ma062599e10.1021/ma062599e ↗
39. 10.1002/anie.19900138110.1002/anie.199001381 ↗
40. 10.1002/rcm.129009151610.1002/rcm.1290091516 ↗
41. 10.1016/j.tca.2004.09.01410.1016/j.tca.2004.09.014 ↗
42. 10.1002/app.3931510.1002/app.39315 ↗
43. 10.1016/0032-3861(88)90182-610.1016/0032-3861(88)90182-6 ↗
44. 10.1021/ma049506i10.1021/ma049506i ↗
45. 10.1021/ma062482q10.1021/ma062482q ↗
46. 10.1122/1.355303210.1122/1.3553032 ↗
47. 10.1021/jp064574n10.1021/jp064574n ↗
48. 10.1134/s0965545x1112003010.1134/s0965545x11120030 ↗
49. 10.1038/nenergy.2016.12910.1038/nenergy.2016.129 ↗
50. 10.1021/je300854w10.1021/je300854w ↗
51. 10.1016/j.tca.2014.07.01210.1016/j.tca.2014.07.012 ↗
52. 10.1007/s10965-009-9300-010.1007/s10965-009-9300-0 ↗
53. 10.1021/ma035663q10.1021/ma035663q ↗
54. 10.1021/ma971045w10.1021/ma971045w ↗
55. 10.1007/bf0039668110.1007/bf00396681 ↗
56. 10.1016/0032-3861(88)90182-610.1016/0032-3861(88)90182-6 ↗
57. 10.1122/1.54985310.1122/1.549853 ↗
58. 10.1002/pen.76027220910.1002/pen.760272209 ↗
59. 10.1021/j100369a08610.1021/j100369a086 ↗
60. Winter H. H. · 1997 · 16510.1007/3-540-68449-2_3 ↗
61. 10.1021/acsami.5b0934410.1021/acsami.5b09344 ↗
62. 10.1007/bf0043730710.1007/bf00437307 ↗
63. 10.1002/polb.1992.09030091310.1002/polb.1992.090300913 ↗
64. 10.1021/ma00178a02010.1021/ma00178a020 ↗
65. Flory P. J. · 1953
66. 10.1038/nature0869310.1038/nature08693 ↗
67. 10.1038/ncomms421810.1038/ncomms4218 ↗
68. 10.1038/453171a10.1038/453171a ↗
69. 10.1002/anie.20170723910.1002/anie.201707239 ↗
70. 10.1021/mz300451r10.1021/mz300451r ↗
71. 10.1016/j.carbpol.2013.11.04510.1016/j.carbpol.2013.11.045 ↗
72. 10.1021/acs.langmuir.5b0347410.1021/acs.langmuir.5b03474 ↗