journal article·2006-09

Polyphenylenesulfied/montomorillonite clay nanocomposite coatings: Their efficacy in protecting steel against corrosion

Toshifumi Sugama

Materials Letters· Volume 60· Issue 21-22
Publisher page

Abstract

Nanoscale montomorillonite (MMT) clay fillers became dispersed in a polyphenylenesulfied (PPS) matrix through the processes of octadecylamine (ODA) intercalation {yields} molten PPS co-intercalation {yields} exfoliation. Cooling this molten exfoliated material led to the formation of a PPS/MMT nanocomposite. The MMT nanofiller conferred three advanced properties on the semi-crystalline PPS: First, it raised its melting point by nearly 40 C to 290 C; second, it increased its crystallization energy, implying that an excellent adherence of the nanofillers surfaces to PPS in terms of a good interfacial bond; and, third, it abated the degree of its hydrothermal oxidation due to sulfide {yields} sulfite linkage transformations. When this advanced PPS nanocomposite was used as a corrosion-preventing coating for carbon steel in a simulated geothermal environment at 300 C, a coating of {approx}150 {micro}m thickness adequately protected the steel against hot brine-caused corrosion. In contrast, an MMT-free PPS coating of similar thickness was not nearly as effective in mitigating corrosion as was the nanocompsite; in fact, the uptake of corrosive ionic electrolyte by the unmodified coating increased with an extending exposure time.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Polymer Nanocomposites and Properties · Tribology and Wear Analysis · Polymer composites and self-healing

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

References (23)

Show source-provided references
1. Sugama · J. Mater. Sci. · 2002 · 37 · 487110.1023/A:1020806012202 ↗
2. Gawlik · Geotherm. Resour. Counc. Trans. · 2003 · 24 · 450
3. Sugama · Geotherm. Resour. Counc. Trans. · 2004 · 28 · 365
4. Sugama · Polym. Polym. Compos. · 2003 · 11 · 16110.1177/096739110301100301 ↗
5. Komori · 2000 · 3
6. Ruiz-Hitzky · 2000 · 18
7. Chen · Polym. Mater. Sci. Eng. · 2002 · 88 · 88
8. Goldstein · J. Eur. Ceram. Soc. · 2004 · 24 · 318710.1016/j.jeurceramsoc.2003.11.013 ↗
9. Lee · Mater. Chem. Phys. · 2004 · 85 · 41010.1016/j.matchemphys.2004.01.032 ↗
10. Pospisil · Colloid Interface Sci. · 2004 · 277 · 15410.1016/j.jcis.2004.04.025 ↗
11. Morgan · Polym. Mater. Sci. Eng. · 2000 · 83 · 53
12. Tidjani · Polym. Degrad. Stab. · 2001 · 74 · 3310.1016/S0141-3910(01)00061-1 ↗
13. Jurkowski · Thermochim. Acta · 2004 · 414 · 24310.1016/j.tca.2004.01.008 ↗
14. Lam · Compos., Part B Eng. · 2005 · 36 · 26310.1016/j.compositesb.2004.09.006 ↗
15. Ray · J. Am. Ceram. Soc. · 1991 · 74 · 6010.1111/j.1151-2916.1991.tb07297.x ↗
16. Kelton · J. Am. Ceram. Soc. · 1992 · 75 · 244910.1111/j.1151-2916.1992.tb05597.x ↗
17. Waddon · J. Mater. Sci. · 1987 · 22 · 177310.1007/BF01132406 ↗
18. Qian · J. Mater. Res. · 1989 · 4 · 100510.1557/JMR.1989.1005 ↗
19. Li · Polymer · 2000 · 41 · 16110.1016/S0032-3861(99)00140-8 ↗
20. Lenz · J. Polym. Sci. · 1960 · 53 · 16710.1002/pol.1960.1204314113 ↗
21. Port · J. Appl. Polym. Sci. · 1979 · 24 · 114510.1002/app.1979.070240501 ↗
22. Farmer · Spectrochim. Acta · 1964 · 20 · 114910.1016/0371-1951(64)80165-X ↗
23. Bellamy · 1975 · 349