journal article·2020-02

Mechanical properties and decomposition performance of peelable coating containing UiO-66 catalyst and waterborne silane-terminated polyurethane dispersions

Kyung-Min Kim, Hee-Woong Park, Gyu-Seong Shim, Seong-Wook Jang, Hyun-Joong Kim, Gyeong-Seok Chae, Seunghan Shin, Jung-Hyun Lee

Journal of Materials Science· Volume 55· Issue 6
Publisher page

Abstract

An easily peelable coating was prepared using silane-terminated polyurethane dispersions (SPUDs) and UiO-66 catalyst (a zirconium(IV)-based metal–organic framework), to capture and decompose the nerve agent simulant, methyl paraoxon (MPO), at room temperature. SPUDs were used as the binder. The peel strength of the SPUD film containing UiO-66 decreased with increasing UiO-66 content, and the film with 40 wt% UiO-66 could not be easily peeled off. In contrast, the SPUD/PVB/UiO-66 peelable coating film could be easily peeled off. With increasing UiO-66 content, the Young’s moduli of the SPUD/UiO-66 and SPUD/PVB/UiO-66 coating films gradually increased, while the elongation decreased. The increase in the glass transition temperature was less than approximately 5%, depending on the UiO-66 content of the SPUD/UiO-66 film. Two peaks of tan δ appeared for the SPUD/PVB/UiO-66 coating film. As the UiO-66 content increased, the second peak shifted to the right. This could be attributed to the bond strength between the mixed polymeric binder and the nanoparticles. Furthermore, MPO decomposition by the SPUD/PVB/UiO-66 coating film increased with increasing UiO-66 content. These findings suggest the possibility of the development of a peelable coating film for the capture and decomposition of MPO.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Conducting polymers and applications · Metal-Organic Frameworks: Synthesis and Applications · Polymer composites and self-healing

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (38)

Show source-provided references
1. Kreno LE, Leong K, Farha OK et al (2012) Metal–organic framework materials as chemical sensors. Chem Rev 112:1105–1125. https://doi.org/10.1021/cr200324t10.1021/cr200324t ↗
2. Lee J, Farha OK, Roberts J et al (2009) Metal–organic framework materials as catalysts. Chem Soc Rev 38:1450–1459. https://doi.org/10.1039/B807080F10.1039/B807080F ↗
3. Liu J, Chen L, Cui H et al (2014) Applications of metal–organic frameworks in heterogeneous supramolecular catalysis. Chem Soc Rev 43:6011–6061. https://doi.org/10.1039/C4CS00094C10.1039/C4CS00094C ↗
4. Li J-R, Sculley J, Zhou H-C (2012) Metal–organic frameworks for separations. Chem Rev 112:869–932. https://doi.org/10.1021/cr200190s10.1021/cr200190s ↗
5. Mason JA, Veenstra M, Long JR (2014) Evaluating metal–organic frameworks for natural gas storage. Chem Sci 5:32–51. https://doi.org/10.1039/C3SC52633J10.1039/C3SC52633J ↗
6. Della Rocca J, Liu D, Lin W (2011) Nanoscale metal–organic frameworks for biomedical imaging and drug delivery. Acc Chem Res 44:957–968. https://doi.org/10.1021/ar200028a10.1021/ar200028a ↗
7. Moghadam PZ, Fairen-Jimenez D, Snurr RQ (2016) Efficient identification of hydrophobic MOFs: application in the capture of toxic industrial chemicals. J Mater Chem A 4:529–536. https://doi.org/10.1039/C5TA06472D10.1039/C5TA06472D ↗
8. Cavka JH, Jakobsen S, Olsbye U et al (2008) A new zirconium inorganic building brick forming metal organic frameworks with exceptional stability. J Am Chem Soc 130:13850–13851. https://doi.org/10.1021/ja805795310.1021/ja8057953 ↗
9. Schaate A, Roy P, Godt A et al (2011) Modulated synthesis of Zr-based metal–organic frameworks: from nano to single crystals. Chem Eur J 17:6643–6651. https://doi.org/10.1002/chem.20100321110.1002/chem.201003211 ↗
10. Liu X, Shen Z-Q, Xiong H-H et al (2015) Hierarchical porous materials based on nanoscale metal–organic frameworks dominated with permanent interparticle porosity. Microporous Mesoporous Mater 204:25–33. https://doi.org/10.1016/j.micromeso.2014.11.00510.1016/j.micromeso.2014.11.005 ↗
11. Katz MJ, Brown ZJ, Colón YJ et al (2013) A facile synthesis of UiO-66, UiO-67 and their derivatives. Chem Commun 49:9449. https://doi.org/10.1039/c3cc46105j10.1039/c3cc46105j ↗
12. Cho KY, Seo JY, Kim H-J et al (2019) Facile control of defect site density and particle size of UiO-66 for enhanced hydrolysis rates: insights into feasibility of Zr(IV)-based metal–organic framework (MOF) catalysts. Appl Catal B Environ 245:635–647. https://doi.org/10.1016/j.apcatb.2019.01.03310.1016/j.apcatb.2019.01.033 ↗
13. Natali I, Carretti E, Angelova L et al (2011) Structural and mechanical properties of “peelable” organoaqueous dispersions with partially hydrolyzed poly(vinyl acetate)-borate networks: applications to cleaning painted surfaces. Langmuir 27:13226–13235. https://doi.org/10.1021/la201578610.1021/la2015786 ↗
14. Lewandowski K, Krepski LR, Mickus DE (2004) Dry-peelable temporary protective coatings from waterborne self-crosslinkable sulfourethane-silanol dispersions. J Appl Polym Sci 91:1443–1449. https://doi.org/10.1002/app.1331610.1002/app.13316 ↗
15. Shirai M, Bamba T, Hayashi K et al (2000) Sheet for protecting paint film
16. Ozeki K, Wada T, Ito K et al (1982) Peelable film-forming urethane/isocyanate paints
17. Rahman MM, Kim H-D, Lee W-K (2009) Properties of waterborne polyurethane adhesives: effect of chain extender and polyol content. J Adhes Sci Technol 23:177–193. https://doi.org/10.1163/156856108X34466710.1163/156856108X344667 ↗
18. Lei L, Zhong L, Lin X et al (2014) Synthesis and characterization of waterborne polyurethane dispersions with different chain extenders for potential application in waterborne ink. Chem Eng J 253:518–525. https://doi.org/10.1016/j.cej.2014.05.04410.1016/j.cej.2014.05.044 ↗
19. Li S, Kong X, Feng S (2015) Preparation of uniform poly(urea-siloxane) microspheres through precipitation polymerization. RSC Adv 5:90313–90320. https://doi.org/10.1039/C5RA18140B10.1039/C5RA18140B ↗
20. Hou Z, Qu W, Kan C (2015) Synthesis and properties of triethoxysilane-terminated anionic polyurethane and its waterborne dispersions. J Polym Res 22:111. https://doi.org/10.1007/s10965-015-0757-810.1007/s10965-015-0757-8 ↗
21. Kim K, Seo JY, Baek K-Y et al (2019) Metal–organic framework (UiO-66)-dispersed polyurethane composite films for the decontamination of methyl paraoxon. Polym Int. https://doi.org/10.1002/pi.585610.1002/pi.5856 ↗
22. Mondloch JE, Katz MJ, Isley WC III et al (2015) Destruction of chemical warfare agents using metal–organic frameworks. Nat Mater 14:512–516. https://doi.org/10.1038/nmat423810.1038/nmat4238 ↗
23. Katz MJ, Mondloch JE, Totten RK et al (2014) Simple and compelling biomimetic metal–organic framework catalyst for the degradation of nerve agent simulants. Angew Chem 126:507–511. https://doi.org/10.1002/ange.20130752010.1002/ange.201307520 ↗
24. Katz MJ, Moon S-Y, Mondloch JE et al (2015) Exploiting parameter space in MOFs: a 20-fold enhancement of phosphate-ester hydrolysis with UiO-66-NH 2. Chem Sci 6:2286–2291. https://doi.org/10.1039/C4SC03613A10.1039/C4SC03613A ↗
25. Mirmohseni A, Akbari M, Najjar R, Hosseini M (2019) Self-healing waterborne polyurethane coating by pH-dependent triggered-release mechanism. J Appl Polym Sci 136:47082. https://doi.org/10.1002/app.4708210.1002/app.47082 ↗
26. Feng L, Iroh JO (2013) Novel polyimide-b-polyurea supramacromolecule with remarkable thermomechanical and dielectric properties. Eur Polym J 49:1811–1822. https://doi.org/10.1016/j.eurpolymj.2013.04.00710.1016/j.eurpolymj.2013.04.007 ↗
27. Maya-Visuet E, Gao T, Soucek M, Castaneda H (2015) The effect of TiO2 as a pigment in a polyurethane/polysiloxane hybrid coating/aluminum interface based on damage evolution. Prog Org Coat 83:36–46. https://doi.org/10.1016/j.porgcoat.2015.02.00110.1016/j.porgcoat.2015.02.001 ↗
28. Wu G, An J, Sun D et al (2014) Robust microcapsules with polyurea/silica hybrid shell for one-part self-healing anticorrosion coatings. J Mater Chem A 2:11614–11620. https://doi.org/10.1039/C4TA01312C10.1039/C4TA01312C ↗
29. Moghaddam ZS, Kaykhaii M, Khajeh M, Oveisi AR (2018) Synthesis of UiO-66-OH zirconium metal–organic framework and its application for selective extraction and trace determination of thorium in water samples by spectrophotometry. Spectrochim Acta A Mol Biomol Spectrosc 194:76–82. https://doi.org/10.1016/j.saa.2018.01.01010.1016/j.saa.2018.01.010 ↗
30. Yuan Y, Zhang Y, Fu X et al (2016) Silane-terminated polyurethane applied to a moisture-curable pressure-sensitive adhesive using triethoxysilane. RSC Adv 6:83688–83696. https://doi.org/10.1039/C6RA19883J10.1039/C6RA19883J ↗
31. Blaine SJ, Wilson KK (1996) Protective solvent free liquid masking compounds and related method. US Patent 5,494,702, 27 Feb, 1996
32. Muller H-P, Gruttmann H, Casselmann H, et al (1999) Cosolvent-free aqueous, anionic polyurethane dispersions and their use as peelable coatings. US Patent 5,965,195, 12 Oct, 1999
33. Salamon PA 54) Temporary protective coatings for precision surfaces. 14
34. Polymeric peel-off coating compositions and methods of use thereof. Google Patents US6124044A. https://patents.google.com/patent/US6124044A/en. Accessed 24 May 2019
35. Adhesion performance of PSA–clay nano-composites by the in situ polymerization and mechanical blending. ScienceDirect. https://www.sciencedirect.com/science/article/pii/S0143749613001395. Accessed 2 July 2019
36. Mahdi EM, Tan J-C (2016) Dynamic molecular interactions between polyurethane and ZIF-8 in a polymer-MOF nanocomposite: microstructural, thermo-mechanical and viscoelastic effects. Polymer 97:31–43. https://doi.org/10.1016/j.polymer.2016.05.01210.1016/j.polymer.2016.05.012 ↗
37. Li P, Klet RC, Moon S-Y et al (2015) Synthesis of nanocrystals of Zr-based metal–organic frameworks with csq-net: significant enhancement in the degradation of a nerve agent simulant. Chem Commun 51:10925–10928. https://doi.org/10.1039/C5CC03398E10.1039/C5CC03398E ↗
38. Long NH, Park H, Chae G et al (2019) Preparation of peelable coating films with a metal organic framework (UiO-66) and self-crosslinkable polyurethane for the decomposition of methyl paraoxon. Polymers 11:1298. https://doi.org/10.3390/polym1108129810.3390/polym11081298 ↗