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Electroactive conducting polymers for corrosion control 总被引:1,自引:0,他引:1
Dennis E. Tallman Geoff Spinks Anton Dominis Gordon G. Wallace 《Journal of Solid State Electrochemistry》2002,6(2):73-84
There is an intensive effort underway to develop new corrosion control coatings for structural metals. In part, this effort
has been motivated by the desire to replace chromium(VI)-containing coatings currently used for corrosion control of iron
and aluminum alloys. Cr(VI) has been shown to be hazardous to the environmental and to human health, and its use in many countries
will be sharply curtailed in the coming years. Electroactive conducting polymers (ECPs) represent a class of interesting materials
currently being explored for use in corrosion control coating systems, possibly as a replacement for Cr(VI)-based coatings.
The electroactivity and the electronic conductivity (or semiconductivity) of ECPs set them apart from traditional organic
coatings. As with chromate, interesting and potentially beneficial interactions of ECPs with active metal alloys such as steel
and aluminum are anticipated, with concomitant alteration of their corrosion behavior. A review of this active research area
will be presented in two parts. Here in Part 1, a general introduction to the topic of corrosion control by ECPs will be presented,
including an overview of corrosion and its control by traditional methods, an introduction to ECPs and their properties, and
a discussion of the processing issues surrounding the use of ECPs as coatings. Part 1 also includes a review of the literature
on the use of ECPs as coatings (or components of coatings) on non-ferrous active metals, principally aluminum and aluminum
alloys, although some work on zinc, copper, silver, titanium and silicon will also be described. In Part 2 of this review
(to be published in the next issue of this journal), the rather extensive literature on the use of ECPs for the corrosion
control of ferrous alloys (steels) will be reviewed.
Electronic Publication 相似文献
3.
Werner Leißner 《Results in Mathematics》1991,20(1-2):530-537
4.
J. B. Lewis E. L. Baldeschwieler L. D. Tabern E. F. Shelberg D. Hillis S. Cromer I. F. Bingham S. Givaudon M. Aubert M. R. Moutte A. Andant P. Lambert J. Lecomte J. Tausz H. Wolf B. Gordon W. Dachnow I. Perrier M. Lobunetz M. O. Chaikin C. Engler D. Holde 《Analytical and bioanalytical chemistry》1940,119(7-8):307-310
5.
Hans Maaß 《Mathematische Annalen》1941,118(1):312-318
Ohne Zusammenfassung 相似文献
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[3,3]-Sigmatropic rearrangements of allyl tetronates and allyl tetramates to give 3-allyltetronic or -tetramic acids, respectively, proceed within 20-60 min under microwave irradiation (300 W, 130-190 °C). Consecutive (homo)sigmatropic [1,5] H-shifts such as oxa-ene reactions are promoted less effectively, which allows the isolation of Claisen intermediates of sigmatropic domino sequences, in contrast to conventional heating. 相似文献
8.
P. Murzyn C. R. Pidgeon P. J. Phillips J. -P. Wells N. T. Gordon T. Ashley J. H. Jefferson T. M. Burke J. Giess M. Merrick B. N. Murdin C. D. Maxey 《Physica E: Low-dimensional Systems and Nanostructures》2004,20(3-4):220
We have made direct pump–probe measurements of spin lifetimes in long wavelength narrow-gap semiconductors at wavelengths between 4 and 10 μm and from 4 to 300 K. In particular, we measure remarkably long spin lifetimes, τs300 ps, even at 300 K for epilayers of degenerate n-type InSb. In this material the mobility is approximately constant between 77 and 300 K, and we find that τs is approximately constant in this temperature range. In order to determine the dominant spin relaxation mechanism we have investigated the temperature dependence of τs in non-degenerate lightly n-type Hg0.78Cd0.22Te of approximately the same band gap as InSb, and find that τs varies from 356 ps at 150 K to 24 ps at 300 K. Our results, both in magnitude and temperature dependence of τs, imply that the Elliott–Yafet model dominates in these materials. 相似文献
9.
Starch belongs to the polyglucan group. This type of polysaccharide shows a broad β-relaxation process in dielectric spectra at low temperatures, which has its molecular origin in orientational motions of sugar rings via glucosidic linkages. This chain dynamic was investigated for α(1,4)-linked starch oligomers with well-defined chain lengths of 2, 3, 4, 6, and 7 anhydroglucose units (AGUs) and for α(1,4)-polyglucans with average degrees of polymerization of 5, 10, 56, 70, and so forth (up to 3000; calculated from the mean molecular weight). The activation energy (Ea) of the segmental chain motion was lowest for dimeric maltose (Ea = 49.4 ± 1.3 kJ/mol), and this was followed by passage through a maximum at a degree of polymerization of 6 (Ea = 60.8 ± 1.8 kJ/mol). Subsequently, Ea leveled off at a value of about 52 ± 1.5 kJ/mol for chains containing more than 100 repeating units. The results were compared with the values of cellulose-like oligomers and polymers bearing a β(1,4)-linkage. Interestingly, the shape of the Ea dependency on the chain length of the molecules was qualitatively the same for both systems, whereas quantitatively the starch-like substances generally showed higher Ea values. Additionally, and for comparison, three cyclodextrins were measured by dielectric relaxation spectroscopy. The ringlike molecules, with 6, 7, and 8 α(1,4)-linked AGUs, showed moderately different types of dielectric spectra. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 188–197, 2004 相似文献
10.
The NH,NH-dihydrocycloadduct 1 (6-chloro-9,9-dimethyl-7,8-dihydro-9H-pyrazolo[4,3-d]tetrazolo[1,5-b]-pyridazine) obtained by the cycloaddition of 2-diazopropane to 6-chlorotetrazolo[1,5-b]pyridazine, is transformed with protected or unprotected carbohydrates 2, 5, 7,9, 11, 13 and 15 in the presence of methyl acrylate ( 3 ) into the corresponding C-nucleosides 4,6,8,10,12,14 and 16 . In this one-pot synthesis two new chiral centers are formed stereoselectively, dependent on the chirality at C-atom next to aldehydo group in the carbohydrate. 相似文献