We wish  to  introduce  the work of the  research group for  corrosion and electrochemistry of 
Institute of Inorganic Chemistry, Technical University of Budapest.  The main fields of our 
investigations were  the electrogalvanizing of palladium-nickel  alloy-coatings,  the study of 
the  sealing  of  the  anodic  oxide-layers,  the  corrosion-resistance  of  titanium-carbide  steel-
alloys,  the effectiveness of inhibitors protecting the steel  reinforcement of cellular concrete 
and  the study of the  corrosion  effect  of chemical  agents  used  for  salting winter  roads

Gál-Solymos, Kamilla

Hencsei , Pál

Lohonyai, Nándor

Schächter, Klára

English

Periodica Polytechnica (Budapest University of Technology and Economics)

PERIODICA POLY7'ECHNICA SER. CHEM. ENG. VOL. 35, NO. 3, PP. 151-157 (1991) CORROSION AND ELECTROCHEMICAL RESEARCHES K. G. SOLn!Os, P. HE!':CSEI, N. LOHONYAI and K. SCHACHTER1 Institute of Inorganic Chemistry Technical University, H-1521 Budapest, Hungary Received: July 15, 1991. Presented by Prof. J. NAGY Abstract We wish to introduce the work of the research group for corrosion and electrochemistry of Institute of Inorganic Chemistry, Technical University of Budapest. The main fields of our investigations were the electrogalvanizing of palladium-nickel alloy-coatings, the study of the sealing of the anodic oxide-layers, the corrosion-re,sistance of titanium-carbide steel-alloys, the effectiveness of inhibitors protecting the steel reinforcement of cellular concrete and the study of the corrosion effect of chemical agents used for salting winter roads. Keywords: corrosion, layers, inhibitors, salting, Introduction The corrosion and electrochemical researches started here more than 40 years ago. Even under tht: leadership of Prof. PROSZT some electrochemi-cal studies were done here and it was the starting point of the study of the surface conditions of metals as well. At first the investigations covered pri-marily the area of metals and alloys, later they focused on different layers and corrosion inhibitors. On the field of the layers among others the fol-lowing materials were studied in our Institute: metallizationed aluminum and zinc-aluminum alloy-layers [1, 2], phosphate-layers [3, 4], silicone-resin-based layers [5, 6], galvanic layers [7-10], chromate layers [11, 12], under-spraying compounds [13]. In the territory of inhibitor study among others the following compounds were investigated: mercaptanes and amines [14], silatranes [15], intermediates of rubber industry [16], surface-active materi-als [17], organic nitrogen-compounds [18]. We would like to introduce some of our results found recently. 1 Research Group of Chemistry for Alkaloids, Hungarian Academy of Sciences H-1521 Bu-dapest, Hungary. 152 K. G. SOLYMOS et al. Palladimu-nickel Alloy-layer Galvanic selection of wear- and corrosion-resistant palladium-nickel alloy-layers was studied [19]. This layer has favourable properties and it is suit-able for the substitution of hard gold used in electronic- and jeweller's trade. The goal of our work was to optimalize the operation parameters of the galvanic-electrolytic addition system of palladium-nickel developed and still in progress at General Design Institute for the Engineering Industry. This electrolyte consisted of moistener and 3 different polishing additives. Phosphoric acid derivatives as moistener [A] and sulfamide derivatives as primary polisher [B] were applied. Secondary polishers [C, D] were pyridine derivatives. The electrolytes of the following compounds were used for the experiment: [Pd(NH3)6]Ch 10g/dm3 [Ni(NH3)s]S04 10g/dm3 (NH4hS04 75g/dm3 A component 0.lg/dm3 B component 2.0g/dm3 C component 0.04 - 0.16g/dm3 D component 0.8g/dm3 The effect of the additives on the cathodic metal separation was stud-ied with the help of potentiodynamic curves. On the effect of the additives the speed of metal separation decreased and the polarization curves shifted to negative direction. It was found that the moistener and the different polishing components cause cathodic polarization of different size. The biggest cathodic polarization (cca. 100 m V) occurred in the presence of 'C' polishing additive. Further on, as a function of 'C' component the composition of the layer and its physical and corrosion properties were studied. The optimal concentration of 'C: polishing additive was determined: 0.08g/dm3• Fi-nally, besides the optimal electrolytic solution-compound, the effect of the mixture of the solution and cathodic electric density on the properties of the obtained layer were observed. In case of mixing the solution, the Pd-contents of the layer grows by the increase of the electric density. The parameters of the metal separation as diffusion-controlled processes are in question - can be better checked. The desired 75 % Pd-concentration can be achieved at 0.8A/dm2 electric density and under such circumstances other properties of the layer also meet the requirements. The optimal galvano-electric compound and the layer produced with optimal operation parameters seem suitable for the substitution of hard gold used in industry. CORROSION AND ELECTROCHEMICAL RESEARCHES 153 Anodic Oxide Layer The structure and properties of anodic oxide layer, which was obtained on aluminum with an electrochemical method, were investigated as a func-tion of the temperature of anodic process [20]. Furnace-aluminum plate with the purity of 99.5 % was used for the experiments. The anodic oxida-tion was carried out in 180g/dm3H2S04 solution containing 3g/dm3 solute aluminum with direct current at cell tension of 16 V. The temperature of the electrolyte was changed by 2°C between 10 and 20°C. In each case 15 JLm thick top layer was formed, which needed 60 (18-20°C), 90 (14-16°C) and 120 minutes (10-12 °C). The oxide layer was tightened in distilled water at 100°C. The morphology, solidity, wear-resistance and corrosion properties of untight and tight top layers formed at different temperatures were studied. Transmission-scanning electron microscopic photos provided informa-tion about the morphology of the layers. Sealing was determined in solu-tions containing H3P04 and K2Cr207 on the basis of solubility (weight loss) and admittance measures. Corrosion-resistance investigations were carried out in NaCl-, CH3COOH- and H202 solutions. It was found that by decreasing the temperature of anodic oxidation the hardness of the layer would grow, at the same time, as a result of sealing the hardness of the top layer would decrease approximately with 40-60 RV. The hardest ones (440 and 510 HV) are the tight and untight layers produced at 10 °C, which belong to the so-called 'hard oxide layers'. The temperature increased by 10°C will result in more than double hardness decrease. . The temperature-dependence of wear-resistance shows a tendency similar to that of hardness. The sealing and corrosion-resistance of the layers improve by cooling. All the above-mentioned data show that the structure of the top-layer considerably changes under 14 °C. The layer be-comes tighter, harder, its mechanical and corrosion properties improve, it is less suitable for post-colouring. Titaniumcarbide-steel Alloys In different medium the corrosion-resistance of titaniumcarbide-steel alloys produced in a powder metallurgical way was studied in co-operation with the Technical University of Tallinn [21] gravimetric, metallographical and electrochemical investigations were carried out. T.he samples investigated were different in TiC contents (50 and 60 %) and in the way they were produced. The corrosion-resistance did not de-pend on the way of production, the bending strength and impact energy, 154 K. G. SOLYAfOS et al. however, showed higher values at samples synthetically created of their elements. The TiC-Fe-Ni-Cr alloys studied in 20 % NaOH solution are com-pletely resistant up to 80 % . The speed of corrosion was measured in 3 % H2S04 solution at different temperatures. In case of 10 % HN03 solution, the measurements were taken only at 20°C due to the quick deterioration of the sample. According to metallographic st udies the basic metal is exposed to corrosion in H2S04 and H3P04 solutions. The carbide-skeleton remains. In HN03 the selective solubility of the carbide component can be observed, so the speed of corrosion grows with the increase of TiC contents of the alloy. The effect of some inhibitors that worked well in case of some carbon steels were examined as well in order to decrease the corrosion of TiC-Fe-Cr-Ni alloys, applying 0.5 % inhibitor. In 10 % HN03 solution thiocar-bamide, in 3 % H2S04 and 44 % H3P04 PKU was used as inhibitor. (PKU= polycondensated product of urotropin, benzyl-chloride and aniline). The inhibitors substantially decrease the speed of corrosion. By temperature increase the ~rotective effect slightly grows. During our further work the corrosion- and wear-resistance of solid alloys (TiC-Fe-Cr) from titanium-carbide and chromium-steel in a powder-metallurgic way were studied in water with corrosion-abrasive, abrasive, gravimetric and electrochemical methods [22]. In the course of the ex-periments in the steel basic metal 33-60 % TiC and 0-25 % chromium-containing alloys were investigated. The corrosion- and wear-resistance of TiC-Fe-Cr alloys were studied in case of corrosion-abrasive and abrasive wear as a function of chromium- and TiC- contents. The corrosion-abrasive wear was measured in either water-containing 0.5 % siliceous sand or 5 % siliceous sand + 0.5 % NaN02 inhibitor. Besides, the intensity of abrasion, in abrasive ray (siliceous sand) as well and also the speed of corrosion in water were investigated. Protection of Steel-reinforcement by Inhibitors The effectiveness of several inhibitors was studied in chloride-containing medium to protect steel-reinforcement of tight (cellular) concrete [23]. Nitrite, chromate, benzoate, phosphate salts and amine-derivatives were used as inhibitors. The investigations were carried out with carbon-steel sample-plate in wet-warm cell and in saturated Ca(OHh + 2 % CaC12-containing corrosive medium. It was found that the best results were achieved in case of the following inhibitor composition: CORROSION AND ELECTROCHEMICAL RESEARCHES 155 NaN02 + R2NH2N02+ morpholine derivatives where R: cyclohexyl. Chemical Agents Used for Salting Winter Roads The corrosion-effect of chemical agents used for exemption the roads in winter of slipperiness was studied [24]. With laboratory examinations the corrosion processes going on in soil were studied. Instead of various soil tests the surface alteration on sample-plates was investigated and corrosion weight-loss was measured. During the experiments soils, sample plates and melting salts showed in Table 1 were applied. Table 1 Model-experiments in laboratory Chemicals for thaw NaC] .\lgC]2 CaCI2 CO(NH2h CaMg( CH 3 COO)4 Test plates Carbon steel (M2H) Aluminum (AI 99.5) Aluminum-alloy (AIMgSi) Corrosion resistant steel (KO 37 Ti) Soils chernoz'om rendzina shifting sand Previously degreased and surface treated and weighed sample-plates put into different types of soils were sprayed with 10 % solution of chemical agents 5 times a week throughout a month, then their weight-loss was determined. It was found that corrosion effect of the materials suitable for exemption of slipperiness decreases according to the following order: The change of the deterioration of the structural material is as follows: Fe > Al > AIMgSi > > K037Ti. Among the types of soils the highest speed of corrosion was measured in the shifting sand, the results in case of rendzina and finally in that of chernoz'om were much better. Finally, let us mention the education of postgraduate corrosion engi-neers also belongs to the work of the group of corrosion and electrochem-ical researches. The education has been regularly going on since 1964. 156 K. G. S6LYMOS et al. 202 experts of this field received postgraduate degree. The students while preparing their diploma-work get into tight connection with the work of this special group. The co-operation is also active in helping the corrosion engineers with writing their MS thesis. Up to now at our Institute more than 40 MS theses have been prepared, which served the basis of several scientific lectures and publications. References 1. SZENTESI, 1. - SCHACHTER, K. - LOHONYAI, N. : Eurocorr'82 conference, Budapest, 1982. Section 1., p. 197. 2. SZIJARTO, A. - LOHONYAI, N. : Eurocorr'82 conference, Budapest, 1982. Section I., p.205. 3. GABOR, T. - NEMES, K. - EGRESSY, 1. - HENCSEI, P. : XXVIII MSZV, Eger, 1985. p.323. 4. GABOR, T. - HENCSEI, P. - NEMES, K. : Mezhdun. simp., Albena, 1986. Dokl. 2, p.341. 5. NAGY, J. - HENCSEI, P. - AMBRUS, L. - BIHATSI, L. - FABULYA-PALFI, E. : XVI. FATIPEC Congress Book, Budapest, 1978. p. 257. 6. AMBRUS, L. - BIHATSI, L. - HENCSEI, P. - FABULYA-PALFI, E. - NAGY, J. : Konf. iiber Oberfiiichenschtitz dtirch organ. Uberzuge. Budapest, 1979. Vortrage, p. 85. 7. AGARDI, 1. - KAHAN, R. - NEMES, K. VII. Galvanotechnisches Symp. Budapest, 1985. Vortrage, p. 9. 8. FURKA, E. - NEMES, K. - KAHAN, R. VII. Galvanotechnisches Symp. Budapest, 1985. Vortrage, p. 96. 9. NEMETHY, J. - HENCSEI, P. : VII. Galvanotechnisches Symp. Btidapest, 1985. Vortrage, p.198. 10. PALOTAS, GY. - NEMES, K. - KAHAN, R. : VII. Galvanotechnisches Symp. Budapest, 1985. Vortrage, p. 227. 11. NEMES, K. - TIHANYI, K. : XXII. Intern. Fachtagung Galvanotechnik . .Jena, 1985. p. 101. 12. NEMES, K. - FARKAS, M. - MARosI, T. - LOHONYAI, N. : Corrosion week. Btidapest, 1988. Lectures, p. 38. 13. HORVATHNE FANTO, E. - HENCSEI, P. : Korrozios Figyelo, Vo!. 27, p. 13 (1987). 14. SCHACHTER, K. - LOHONYAI, N. - KALLAST, V. - TALIMETS, E. : Trudi Tallinsk. Politekhn. Inst. Nr. 542,95 (1983). 15. HENCSEI, P. : Korrozios Figyelo, Vo!. 22, p. 74 (1982). 16. SCHACHTER, K. - LOHONYAI, N. : Korrozios Figyelo, Vo!. 24, p. 12 (1984). 17. KALLAST, V. - KUUSK, A. - METSMAA, T. - ALLIKMAA, V. - SCHACHTER, K. -LOHONYAI, N. : Korrozios Figyel5, Vo!. 30, p. 85 (1990). 18. JUHASZ, T. F. : unpublished data. 19. TOTH, E. : Thesis for getting B.Sc. graduation (1989). 20. KATUS, L. : Thesis for getting M.Sc. graduation (1989). 21. KALLAST, V. - KUBARSEPP, J. - SCHACHTER, K. - LOHONYAI, N. : Period. Poly-techn. Chem. Eng. Vo!. 31, p. 213 (1987). 22. SCHACHTER, K. - KALLAST, V. - KUBARSEPP, J. - LOHONYAI, N. : Corrosion week. Budapest, 1988. Lectures, p. 147. CORROSION AND ELECTROCHEMICAL RESEARCHES 157 23. SCHACHTER, K. - TALIMETS, E. - ROHUMAGI, E. - LOHONYAI, N. : Corrosion week. Budapest, 1988. Lectures, p. 24. 24. HENCSEI, P. - GAL-SOLYMOS, K. : V. Intern. Symp. on Corrosion in Soil. Bala-tonszeplak, 1990. Abstracts, p. 16. Addresses: Kamilla GAL-SOLYMOS, PaI HENCSEI and Nandor LOHONYAI Institute of Inorganic Chemistry Technical University H-1521 Budapest Hungary Klara SCHACHTER Research Group of Chemistry for Alkaloids Hungarian Academy of Sciences H-1521 Budapest Hungary 

CORROSION AND ELECTROCHEMICAL RESEARCHES

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CORROSION AND ELECTROCHEMICAL RESEARCHES

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