Marine Biofouling Resistance of Polyurethane with Biodegradation and Hydrolyzation
Source abstract
Abstract
We have prepared polyurethane with poly(ε-caprolactone) (PCL) as the segments of the main chain and poly(triisopropylsilyl acrylate) (PTIPSA) as the side chains by a combination of radical polymerization and a condensation reaction. Quartz crystal microbalance with dissipation studies show that polyurethane can degrade in the presence of enzyme and the degradation rate decreases with the PTIPSA content. Our studies also demonstrate that polyurethane is able to hydrolyze in artificial seawater and the hydrolysis rate increases as the PTIPSA content increases. Moreover, hydrolysis leads to a hydrophilic surface that is favorable to reduction of the frictional drag under dynamic conditions. Marine field tests reveal that polyurethane has good antifouling ability because polyurethane with a biodegradable PCL main chain and hydrolyzable PTIPSA side chains can form a self-renewal surface. Polyurethane was also used to carry and release a relatively environmentally friendly antifoulant, and the combined system exhibits a much higher antifouling performance even in a static marine environment.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Marine Biology and Environmental Chemistry · Microplastics and Plastic Pollution · Polymer Surface Interaction Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Faculty of Materials Science and Engineering, South China University of Technology, Guangzhou 510640, People’s Republic of China
Hefei National Laboratory for Physical Sciences at Microscale, Department of Chemical Physics, University of Science and Technology of China, Hefei 230026, People’s Republic of China
References (46)
Show source-provided references
1. Yebra D. M. · Prog. Org. Coat. · 2004 · 50 · 7510.1016/j.porgcoat.2003.06.001 ↗
2. Schultz M. P. · Biofouling · 2011 · 27 · 8710.1080/08927014.2010.542809 ↗
3. Callow J. A. · Nat. Commun. · 2011 · 2 · 24410.1038/ncomms1251 ↗
4. Finnie, A.; Williams, D. N.InPaint and Coatings Technology for the Control of Marine Fouling in Biofouling;Durr, S.; Thomason, J. C., Eds.Wiley-Blackwell:Chichester, U.K., 2010; p429.10.1002/9781444315462.ch13 ↗
5. Thomas K. V. · Biofouling · 2010 · 26 · 7310.1080/08927010903216564 ↗
6. Lejars M. · Chem. Rev. · 2012 · 112 · 434710.1021/cr200350v ↗
7. Beigbeder A. · Biofouling · 2008 · 24 · 29110.1080/08927010802162885 ↗
8. Gudipati C. S. · J. Polym. Sci., Part A: Polym. Chem. · 2004 · 42 · 619310.1002/pola.20466 ↗
9. Krishnan S. · Langmuir · 2006 · 22 · 507510.1021/la052978l ↗
10. Wang Y. P. · Langmuir · 2011 · 27 · 1036510.1021/la202427z ↗
11. Wang Y. P · Macromolecules · 2011 · 44 · 87810.1021/ma102271t ↗
12. Wang Y. P. · Biofouling · 2011 · 27 · 113910.1080/08927014.2011.629344 ↗
13. Zhang Z. · Langmuir · 2009 · 25 · 1351610.1021/la901957k ↗
14. Jiang S. Y. · Adv. Mater. · 2010 · 22 · 92010.1002/adma.200901407 ↗
15. Xie L. Y. · Polymer · 2011 · 52 · 373810.1016/j.polymer.2011.06.033 ↗
16. Thorlaksen P. · Gallois Mag. · 2010 · 5 · 218
17. Bressy, C.; Margaillan, A.; Faÿ, F.; Linossier, I.; Vallée-Réhel, K.InAdvances in Marine Antifouling Coatings and Technologies;Hellio, C.; Yebra, D. M., Eds.Woodhead Publishing:Cambridge, U.K., 2009; p459.10.1533/9781845696313.3.445 ↗
18. Almeida M. · Prog. Org. Coat. · 2007 · 59 · 210.1016/j.porgcoat.2007.01.017 ↗
19. Fukuda, S.; Honda, Y.; Itoh, M.; Masuoka, S.; Taniguchi, M.Metal-Free Binders for Self-Polishing Antifouling Paints. U.S. Patent 5,436,284, 1995.
20. Oya, M.; Nakamura, N.; Tsuboi, M.Antifouling Coating Composition, Coating Film Therefrom, Base Material Covered with the Coating Film and Antifouling Method. U.S. Patent 6,916,860 B2, 2005.
21. Longo, F. N.; Gardega, T.Polymer Based Antifouling Coating. U.S. Patent219944 A1, 2008.
22. Bressy C. · Polym. Degrad. Stab. · 2010 · 95 · 126010.1016/j.polymdegradstab.2010.03.017 ↗
23. Bressy C. · Prog. Org. Coat. · 2014 · 77 · 66510.1016/j.porgcoat.2013.12.004 ↗
24. Ma C. F. · J. Mater. Chem. B · 2013 · 1 · 309910.1039/c3tb20454e ↗
25. Liu G. B. · Adv. Synth. Catal. · 2007 · 6 · 80710.1002/adsc.200600338 ↗
26. Liu G. B. · Synlett · 2006 · 9 · 143110.1055/s-2006-941576 ↗
27. Ma C. F. · ACS Appl. Mater. Interfaces · 2011 · 3 · 45510.1021/am101039q ↗
28. Ma C. F. · J. Mater. Chem. A · 2013 · 1 · 535310.1039/c3ta00123g ↗
29. Ding M. M. · Biomacromolecules · 2009 · 10 · 285710.1021/bm9006826 ↗
30. Han J. · Front. Mater. Sci. China. · 2009 · 3 · 2510.1007/s11706-009-0013-4 ↗
31. Sivakumar C. · Eur. Polym. J. · 2009 · 45 · 232910.1016/j.eurpolymj.2009.05.003 ↗
32. Sauerbrey G. · Z. Phys. · 1959 · 155 · 20610.1007/BF01337937 ↗
33. Voinova M. V. · Phys. Scr. · 1999 · 59 · 39110.1238/Physica.Regular.059a00391 ↗
34. Liang H. M. · Sens. Actuators, B · 2010 · 149 · 21210.1016/j.snb.2010.05.048 ↗
35. Liu J. T. · Anal. Chim. Acta · 2011 · 703 · 8010.1016/j.aca.2011.07.019 ↗
36. Yu J. · Biofouling · 2003 · 19 · 8310.1080/0892701031000063820 ↗
37. Rutkowska M. · Pol. J. Environ. Stud. · 2002 · 4 · 413
38. Hou Y. · Polymer · 2007 · 48 · 634810.1016/j.polymer.2007.08.054 ↗
39. Rodahl M. · Rev. Sci. Instrum. · 1995 · 66 · 392410.1063/1.1145396 ↗
40. Dovrzynski P. · Biomacromolecules · 2005 · 6 · 48310.1021/bm0494592 ↗
41. Gu X. Z. · Biomacromolecules · 2011 · 12 · 306610.1021/bm2006938 ↗
42. Vogt B. D. · J. Phys. Chem. B · 2004 · 108 · 1268510.1021/jp0481005 ↗
43. Hong F. · Polymer · 2013 · 54 · 296610.1016/j.polymer.2013.04.010 ↗
44. Faÿ F. · Eur. Polym. J. · 2007 · 43 · 480010.1016/j.eurpolymj.2007.07.045 ↗
45. Bellenger V. · Polym. Degrad. Stab. · 1995 · 49 · 9110.1016/0141-3910(95)00049-R ↗
46. Báez J. E. · Macromolecules · 2012 · 45 · 696610.1021/ma300990s ↗