YU-ISSN 0352-5139 J.Serb.Chem.Soc. Vol. 68, No. 6 (2003) CONTENTS Organic Chemistry A. S. Veli~kovi}, M. S. Risti}, D. T. Veli~kovi}, S. N. Ili} and N. D. Miti}: The possibilities of the application of some species of sage (Salvia L.) as auxiliaries in the treatment of some diseases 435 M. Carposu, L. Odochian, St. Dima. M. Dumitras and M. Petrovanu: Thermokinetic study of the inactivation reaction of 1-methyl phthalazinium ylids 447 Inorganic Chemistry R. N. Prasad and N. Gupta: Termplate synthesis of Mn(II) complexes of tetraaazamacrocycles derived from diaminoalkanes and 3,4-hexanedione or benzil 455 M. G. Abd El Wahed: Thermodynamic and structural studies of complexes of manganese(II), cobalt(II), nickel(II) and copper(II) with aminofuropyridine carboxamide (Note) 463 D. Vu~ini}, I. Miljanovi}, A. Rosi} and P. Lati}: Effect of Na2O/SiO2 mole ratio on the crystal type of zeolite synthesized from coal fly ash 471 Physical Chemistry J. D. Jovanovi} and D. K. Grozdani}: Saturated-liquid heat capacity: new polynomial models and review of the literature experimental data (Note) 479 Electrochemistry V. Vojinovi}, S. Mentus and V. Komneni}: Thermodynamic and kinetic behavior of hydrogen electrode in a solution of 0.5 M KClO4 in dimethyl sulphoxide 497 Materials B. Matovi}, S. Bo{kovi} and M. Logar: Preparation of basalt-based glass ceramics 505 K. I. Popov, S. B. Krsti} and M. G. Pavlovi}: The critical apparent density for the free flow of copper powder (Preliminary communication) 511 J.Serb.Chem.Soc. 68(6)435–445(2003) UDC 635.74.004.14:615.85 JSCS – 3059 Original scientific paper The possibilities of the application of some species of sage (Salvia L.) as auxiliaries in the treatment of some diseases ANA S. VELI^KOVI]1, MIHAILO S. RISTI]2, DRAGAN T. VELI^KOVI]3, STEVAN N. ILI]4 AND NATA[A D. MITI]3 1Medical Center “Mo{a Pijade”, Department of General Practice, Rade Kon~ara St. 2, 16000 Leskovac, 2Institute for Medicinal Plants Research “Dr. Josif Pan~i}”, Tadeu{a Ko{}u{ka St. 1, 11000 Belgrade, 3AD “Zdravlje” Pharmaceutical and Chemical Industry, Vlajkova St. 199, 16000 Leskovac and 4Faculty of Medicine, Bra}e Taskovi} St. 81, 18000 Ni{, Serbia and Montenegro (Received 5 November 2002) Abstract: The chemical composition of four essential oils of four species of sage (Salvia officinalis L., Salvia pratensis L., Salvia glutinosa L. and Salvia aethiopis L.) are examined by GC-FID and GC-MS analysis. The presence of some components in the essential oil (mono- and sesquiterpene) determines the pharmacological effects and therapeutical application of a plant species. Salvia officinalis L. gives the highest yield of oil (1.1 %), while the lowest is in Salvia pratensis L. (0.1 %). The investigations included the determination of the antimicrobic activities of the essential oils by the diffusion method and the oil of Salvia pratensis L. proved to have the highest activity. Keywords: diseases, therapy, auxiliaries, Salvia L., antimicrobial activity, essential oils, extracts. REFERENCES 1. I. C. Hedge, in Advances in Labiate Science, R. Harley, T. Reynolds Eds., Roy. Bot. Gard., Kew., UK, 1992, p. 85 2. N. Dikli}, in Flora of Serbia VI, M. Josifovi} Ed., SANU, Belgrade, 1974, p. 432 3. N. F. Danilevski, T. V. Zincenko, N. A. Kadola, Zdorovja, Kiev, 1984 4. K. Osawa, T. Matsumoto, H. Yasuda, T. Kato, Y. Naito, K. Okuda, Bull. Tokyo Dent. Coll. 32 (1991) 1 5. V. N. Dobrynin, M. N. Kolosov, B. K. Chernov, N. A. Derbentseva, Khim. Prir. Soedin. (5) (1976) 686 6. L. Perry, Herbal Teas, University of Vermont as a part of PSS123 course, Canada, 1997 7. J. B. Hinou, C. E. Harvala, E. B. Hinou, Pharm. 44 (1989) 302 8. A. Pauli, K. Knobloch, Z. Lebensm. Unters. Forsch. 185 (1987) 10 9. D. Veli~kovi}, M. Risti}, N. Randjelovi}, A. [melcerovi}, J. Essent. Oil Res. 14 (2002) 453 10. M. Armaka, E. Papanikolaou, A. Sivropoulou, M. Arsenakis, Antiviral Res. 43 (1999) 79 11. M. Tada, K. Okuno, K. Chiba, E. Ohnishi, T. Yoshii, Phytochemistry. 35 (1994) 539 12. Rote Liste, ECV Edicio cantor, Aulendorf Württ., 1997 13. E. A. Reverned, “Herbal Combinations”, in The Herbal Encyclopedia, London Press, UK, 1998 14. R. Mabez, The New Age Herbalist. Collier Books, New York, 1988, p. 72 15. M. Grieve, Dover Publications 2 (1971) 700 16. G. F. Secchi, Estratti vegetali, Reppresentanze industriali commercio prodotto chimici, 1991 17. The Macdonald Encyclopedia of Medicinal Plants, 3rd ed., McDonald, Great Britain, 1993 18. J. McGimpsey, Sage-Salvia officinalis. Redbank Research Station, New Zealand Institute for Crop & Food Research Limited, Private Bag 4707, Christchurch, New Zealand, 1996 19. K. N. Sanecky, The Complete Book of Herbs. 2nd ed., McDonald and Janes Publishers, 1975, p. 168 20. D. Baricevic, S. Sosa, R. Della Loggia, A. Tubaro, B. Simonovska, A. Krasna, A. Zupancic, J. Ethnopharmacol. 75 (2001) 125 21. M. Wang, J. Li, M. Rangarajan, Y. Shao, E. J. La Voie, J. Agric. Food Chem. 46 (1998) 4869 22. M. Hernandez-Perez, R. M. Rabanal, M. C. de la Tore, B. Bodriguez, Planta Med. 61 (1995) 505 23. M. J. Ga{i}, Essential oils, Institute for Chemistry, Technology and Metallurgy - Belgrade, Belgrade, 1985 24. M. H. Boelens, H. Boelens, Perfurm. Flavor. 22 (1997) 1 25. B. Lawrence, Perfum. Flavor. 23 (1998) 47 26. J. C. Chalchat, M. S. Gorunovi}, S. D. Petrovi}, Z. A. Maksimovi}, J. Essent. Oil. Res. 13 (2001) 416 27. D. Veli~kovi}, M. Risti}, N. Randjelovi}, V. Stamenkovi}, Lek. sirov. 47 (1998) 75 28. F. Senatore, V. De Feo, J. Essent. Oil Res. 10 (1998) 135 29. Lj. Merkulov, R. Igi}, N. Mimica-Duki}, P. A. Boza, Arch. Pharm. (3–4) (2000) 308 30. N. Stojanov, B. Ahtarov, Wild Useful Herbs in Bulgaria, BAN, Sofia, 1960 31. J. C. Chalchat, S. D. Petrovi}, Z. A. Maksimovi}, M. S. Gorunovi}, Arch. Pharm. (3–4) (2000) 310 32. D. Veli~kovi}, N. Randjelovi}, M. Risti}, A. [melcerovi}, A. Veli~kovi}, J. Serb. Chem. Soc. 67 (2002) 639 33. F. I. Jean, G. J. Collin, D. Lord, Perfurm. Flavor. 17 (1992) 35 34. E. Reverchon, R. Taddeo, G. Della Porta, J. Supercrit. Fluids 8 (1995) 302 35. R. Länger, Ch. Mechtler, J. Jurenitsch, Phytochem. Anal. 7 (1996) 289 36. Pharmacopeia Jugoslavica IV, Edition of the Federal Institute for Health Care, Belgrade 1991 37. R. P. Adams, Identification of Essential Oil Components by Gas Chromatography/Quadrupole Mass Spectroscopy, Allured Publ. Corp., Carol Stream, Illinois, 2001 38. R. P. Adams, Identification of Essential Oil Components by GC/MS, Allured Publ. Corp., Carol Stream, Illinois, 1995 39. D. Veli~kovi}, M. Risti}, A. Veli~kovi}, Lek. sirov. 21 (2001) 51 40. Anonymous, Draft International Standard ISO/DIS 11024-1.2/2.2, Essential oils - General guidance on chromatographic profiles, International Organization for Standardization, Geneva 1997 41. B. Karaka{evi}, Microbiology and Parasitology, Book of Medicine, Belgrade-Zagreb, 1969. J.Serb.Chem. Soc. 68(6)447–453(2003) UDC 66.021.4:547.852.7 JSCS – 3060 Original scientific paper Thermokinetic study on the inactivation reactions of 1-methylphthalazinium ylids MARIA CAPROÔU*, LUCIA ODOCHIAN*, ÔT. DIMA**, M. DUMITRAÔ* and MAGDA PETROVANU* *The “Al. I. Cuza” University, Faculty of Chemistry, Bd. Copou 11, Iasi 6600, Romania and **The “Dunarea de jos” University, Galati, Romania (Received 11 October 2002, revised 9 January 2003) Abstract: The present paper consists in a thermokinetic study on the dimerization reactions of 1methylphthalazinium ylids with –NO2 (ylid 1) and, respectively, –O–CH3 (ylid 2) substituents in the p position of the benzoyl radical bound to the ylidic carbanion. From experimental data, the reaction order and rate constants have been calculated. The reaction order n = 2 confirmed the ylids’ dimerization reactions, while the values of the rate constants, k2 = 3.093 ´10-2 L/mol s and, respectively, 2.16 ´ 10-1 L/mol s for the dimerization of ylids 1 and 2 made evident the higher reactivity of ylid 2 versus ylid 1. The same conclusion is also supported by the results of the thermodynamic study based on the chemical affinity of the two reactions, when Aodim,1 < Aodim,2. Keywords: 1-methylphthalazinium ylids, dimerization, inactivation, thermokinetics (reaction order, rate constants, chemical affinity). REFERENCES 1. I. Zugr|vescu, M. Petrovanu, N-Ylid Chemistry, Mc Graw Hill, London 1976 2. St. Dima, I. Mangalagiu, M. CaproÕu, M. Petrovanu, Ann. Sci. Univ. IaÕi (sl. c.) 4 (1996) 151 3. St. Dima, I. Mangalagiu, M. CaproÕu, M. Petrovanu, J. Serb. Chem. Soc. 62 (1997) 105 4. St. Dima, I. Mangalagiu, M. CaproÕu, M. Petrovanu, Ann. Sci. Univ. Iasi (sl. c.) 5 (1997) 000 5. A. P. Kreskov, L. N. Bikova, N. A. Kazarian, Titrarea in medium neapos, Ed. Tehnic|, BucureÕti, 1969 6. D. J. Pietrzyk, C. W. Frank, Analytical Chemistry, Academic Press, New York, 1980 7. M. CaproÕu, M. Riman, I. Olariu, St. Dima. I. Mangalagiu, M. Petrovanu, J. Heterocyclic Chem. 38 (2001) 495 8. M. J. Pilling, P. W. Seakins, Reaction Kinetics, Oxford Univ. Press, 1996, p. 9 9. N. Aelenei, Gh. Ionescu, O. Roman, M. I. Popa, Bul. Inst. Politehnic Iasi XLIV (XLVIII) (1998) 27 10. J. Sedey, Semi-Empirical Methods of Quantum Chemistry, Wiley, New York 1985, pp. 130 – 135 11. St. Dima, I. Mangalagiu, M. CaproÕu, M. Petrovanu, Ann. Sci. Univ. Iasi (sl. c.) 5 (1997) 001 12. G. Bourceanu, P. Joulain, L. Gbahoue, V. Locquet, Entropie 170 (1992) 17. J.Serb.Chem.Soc. 68(6)455–461(2003) UDC 547.21+547.639.1:542.913:543.4 JSCS – 3061 Original scientific paper Template synthesis of Mn(II) complexes of tetraazamacrocycles derived from diaminoalkanes and 3,4hexanedione or benzil RAGHU N. PRASAD and NITIN GUPTA Department of Chemistry, University of Rajasthan, Jaipur-302 004, India (e-mail: prasadraghunandan@yahoo.com) (Received 31 October 2002, revised 8 January 2003) Abstract: Template condensation of a-diketones, such as 3,4-hexanedione or benzil, with 1,ndiaminoalkanes (where n = 4, 5, 6, 7, 8, 9, 10 or 12) in the presence of Mn(II) resulted in the formation of complexes of the type [MnL(NO3)]NO3 (where L = 16 to 32-membered macrocycle). These complexes have been characterized by elemental analyses, conductances, magnetic measurements, as well as IR and electronic spectra. Keywords: macrocyclic complexes, manganese complexes, IR spectra, electronic spectra. REFERENCES 1. W. A. Welsh, G. J. Reynolds, P. M. Henry, Inorg. Chem. 16 (1977) 2558 2. Y. K. Bhoon, R. P. Singh, Inorg. Nucl. Chem. 43 (1981) 1685 3. R. P. Shukla, R. Rastogi, N. Ahmad, G. Narain, J. Indian Chem. Soc. 65 (1988) 663 4. R. N. Prasad, S. Malhotra, J. Serb. Chem. Soc. 57 (1992) 171 5. R. N. Prasad, A. K. Gupta, P. K. Rai, J. Prakt. Chem. 333 (1991) 145 6. D. S. Eggleston, S. C. Jackels, Inorg. Chem. 19 (1980) 1593 7. V. L. Goedken, J. Molin-case, G. G. Cristoph, Inorg. Chem. 12 (1974) 2894 8. J. L. Hoard, M. J. Hamor, T. A. Hamor, W. S. Gaughey, J. Am. Chem. Soc. 87 (1965) 2312 9. L. Y. Martin, L. J. DeHayes, L. J. Zompa, D. H. Busch, J. Am. Chem. Soc. 96 (1974) 4046 10. V. J. Thom, R. D. Hancock, J. Chem. Soc. Dalton Trans. (1985) 1877 11. R. D. Hancock, M. P. Ngwenya, J. Chem. Soc. Dalton Trans. (1987) 2911 12. J. de O. Cabral, M. F. Cabral, W. J. Cummins, M. G. B. Drew, A. Rodgers, S. M. Nelson, Inorg. Chim Acta 30 (1978) L313 13. M. G. B. Drew, A. H. bin Othman, S. G. Mcfall, P. D. A. McIlroy, S. M. Nelson, J. Chem. Soc. Dalton Trans. (1977) 1173 14. M. J. Maroney, N. J. Rose, Inorg. Chem. 23 (1984) 2252 15. S. C. Jackels, K. Farmery, E. K. Barefield, N. J. Rose, D. H. Busch, Inorg. Chem. 11 (1972) 2893 16. N. A. P. K. Maguire, K. C. Wallace, D. B. Miller, Inorg. Chem. 24 (1985) 597 17. N. W. Alcock, E. H. Curson, N. Herron, P. Moore, J. Chem. Soc. Dalton Trans. (1987) 1979 18. J. Lewis, T. D. O’Donoghue, P. R. Raithby, J. Chem. Soc. Dalton Trans. (1980) 1383 19. K. C. Satpathy, A. K. Panda, R. Mishra, P. Mishra, S. K. Pradhan, J. Indian Chem. Soc. 69 (1992) 49 20. P. S. Mane, S. G. Shirodkar, T. K. Chondhekar, J. Indian Chem. Soc. 79 (2002) 376 21. F. Cariati, D. Galizzioli, F. Morazzoni, L. Naldini, Inorg. Nucl. Chem. Lett. 9 (1973) 742 22. R. H. Holm, G. W. Everett, Jr., A. Chakravorty, Prog. Inorg. Chem. 7 (1966) 83 23. M. C. Weiss, V. L. Goedken, J. Chem. Soc. Chem. Commun. (1976) 531. J.Serb.Chem.Soc. 68(6)463–470(2003) UDC 547.821+547.831:536.7.004.12 JSCS – 3062 Note NOTE Thermodynamic and structural studies of complexes of manganese(II), cobalt(II), nickel(II) and copper(II) with aminofuropyridine carboxamide M. G. ABD EL WAHED Faculty of Science, Zagazig University, Zagazig, Egypt (Received 11 September 2002, revised 27 January 2003) Abstract: Complexes of Mn(II), Co(II), Ni(II) and Cu(II) with 2-aminofuro[3,2-b]pyridine-3-carboxamide have been prepared. The stability constants of the formed complexes were determined at 20, 30, 40 and 50 ºC at a fixed ionic strength, I = 0.1 mol dm-3 (KCl). The values of the thermodynamic functions associated with complex formation were calculated and analyzed in terms of electrostatic and non-electrostatic components. The complexes were characterized with the help of chemical and spectral data. Keywords: aminofuropyridine carboxamide, thermodynamic, conductometric, photometric, spectral properties. REFERENCES 1. R. K. 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J.Serb.Chem.Soc. 68(6)471–478(2003) UDC 549.67+666.122.2/.362–492.2:542.913 JSCS – 3063 Original scientific paper Effect of Na2O/SiO2 mole ratio on the crystal type of zeolite synthesized from coal fly ash DU[ICA VU^INI]1,, IGOR MILJANOVI]1, ALEKSANDRA ROSI]1 and PREDRAG LAZI]1 1Faculty of Mining and Geology, Dju{ina 7, 11000 Belgrade, Serbia and Montenegro (Received 11 September, revised 5 December 2002) Abstract: Coal fly ash was modified to zeolitic materials by hydrothermal treatment at 90 ºC. The zeolite synthesis was studied as a function of the mole ratio of Na2O/SiO2 in the reaction mixtures. The results showed that NaP1 zeolite is obtained when the Na2O/SiO2 mole ratio was 0.7. Hydroxysodalite is the dominant zeolite phase in modified fly ash treated with a higher Na2O concentration solution (Na2O/SiO2 = 1.3). The IR and XRD methods were used to determine the phases present in the starting sample and in the zeolitic materials. Keywords: coal fly ash, hydrothermal treatment, zeolitic materials. REFERENCES 1. D. W. Breck, Zeolites Molecular Sieves, Wiley, New York, 1971 2. H. Höller, U. Wirsching, Fortschr. Miner. 63 (1985) 21 3. F. Mondragon, F. Rincon, L. Sierra, J. Escobar, J. Ramirez, J. Fernandez, Fuel 69 (1990) 263 4. M. Shigemoto, H. Hayashi, K. Miyaura, J. Mater. Sci. 28 (1993) 4781 5. C. Lin, H. Hsi, Environ. Sci. Technol. 29 (1995) 1109 6. X. Querol, F. Plana, A. Alastuey, A. Lopez-Soler, Fuel 76 (1997) 793 7. X. Querol, F. Plana, A. Alastuey, A. Lopez-Soler, J. M. Andres, J. Juan, P. Ferrer, C. R. Ruiz, Environ. Sci. Technol. 31 (1997) 2527 8. C. D. Woolard, K. Petrus, M. van der Horst, ISSN 0378-4738 = Water SA 26 (2000) 531 9. N. Moreno, X. Querol, C. Ayora, Environ. Sci. Technol. 35 (2001) 3526 10. N. Moreno, X. Querol, C. Ayora, A. Alastuey, C. Fernandez-Pereira, M. Janssen-Jurcovicova, J. Environ. Eng. 127 (2001) 994 11. N. Murayama, H. Yamamoto, Junji Shibata, Int. J. Miner. 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J.Serb.Chem.Soc. 68(6)479–495(2003) UDC 66.011+536.412:517.538 JSCS – 3064 Note NOTE Saturated-liquid heat capacity: new polynomial models and review of the literature experimental data JOVAN D. JOVANOVI] and DU[AN K. GROZDANI] Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, 11000 Belgrade, Serbia and Montenegro (Received 18 December 2002) Abstract: In this paper a review of selected literature experimental data for saturated-liquid heat capacities was presented. Two-, three- and four-parameter polynomial correlation models are tested on those data. Obtained results lead to the conclusion that correlation quality depends on the number of parameters, and slightly on the type of models. The best two-, three- and four-parameter models were proposed. Keywords: heat capacity, saturated-liquid heat capacity, correlation, polynomial model. REFERENCES 1. D. Ambrose, J. E. Connett, J. H. S. Green, J. L. Hales, A. J. Head, F. J. Martin, J. Chem. 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KOMNENI] Faculty of Metallurgy and Technology, 81000 Podgorica and 1Faculty of Physical Chemistry, University of Belgrade, Studentski trg 12, 11000 Belgrade, Serbia and Montenegro (Received 22 August 2002, revised 3 March 2003) Abstract: The hydrogen electrode on an interface platinum/dimethyl sulphoxide + 0.5 M KClO4 solution was examined from both the thermodynamic and kinetic aspect, using HCl as a proton source. The equilibrium potential was shown to obey a Nernstian dependence on concentration. The voltammograms recorded using a rotating platinum disc electrode evidenced that the cathodic evolution of hydrogen proceeds under mixed, activation–diffusion control. The diffusion coefficient of the proton was determined to amount to 4.5´10-6 cm2 s-1. In the region of activation control, a Tafel slope of about 0.110 V dec-1 was estimated, which indicates that the Volmer reaction is the rate determining step. Keywords: dimethyl sulphoxide, equilibrium potential, hydrogen electrode, hydrogen evolution, rotating disc. REFERENCES 1. R. Koksbang, J. Baker, H. Shi, M. Y. Saidi, Solid State Ionics 84 (1996) 1 2. J. Zhang, D. K. Benson, C. E. Tracy, S. K. Deb, A. W. Czanderna, R. S. Crandall, J. Electrochem. Soc. 141 (1994) 2795 3. X. Lui, T. Osaka, J. Electrochem. Soc. 144 (1997) 3066 4. D. Mao, M. A. Ibrahim, A. J. Frank, J. Electrochem. Soc. 145 (1998) 121 5. J. N. Butler, J. Electroanal. Chem. 14 (1967) 89 6. J. Simonet, The Electrochemical Reactivity of Sulphones and Sulphoxides, in The Chemistry of Sulphones and Sulphoxides, S. Patai, Z. Rappoport and C. J. M. Stirling, Eds., Wiley, 1988 7. J. A. Olabe, M. C. Giordano, A. J. Arvia, Electrochim. Acta 12 (1967) 907 8. J. A. Bolzan, A. J. Arvia, Electrochim. Acta 15 (1970) 39 9. J. A. Bolzan, A. J. Arvia, Electrochim. Acta 15 (1970) 827 10. M. Sprio, Physical Chemistry of Organic Solvent Systems, A K. Kovington and T. 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J.Serb.Chem.Soc. 68(6)505–510(2003) UDC 666.11–033.4:552.323:666.11.01 JSCS – 3066 Original scientific paper Preparation of basalt-based glass ceramics BRANKO MATOVI]1, SNE@ANA BO[KOVI]1 and MIHOVIL LOGAR2 1The Vinca Institute of Nuclear Sciences, P. O. Box 522, 11001 Belgrade and 2Faculty of Mining and Geology, Department of Mineralogy, Dju{ina 7, Belgrade, Serbia and Montenegro (Received 4 March 2002) Abstract: Local and conventional raw materials–massive basalt from the Vrelo locality on Kopaonik mountain–have been used as starting materials to test their suitability for the production of glass-ceramics. Crystallization phenomena of glasses of the fused basalt rocks were studied by X-ray phase analysis, optical microscopy and other techniques. Various heat treatments were used, and their influences, on controlling the microstructures and properties of the products were studied with the aim of developing high strength glass-ceramic materials. Diopside CaMg(SiO3)2 and hypersthene ((Mg,Fe)SiO3) were identifies as the crystalline phases. The final products contained considerable amounts of a glassy phase. The crystalline size was in range of 8–480 mm with plate or needle shape. Microhardness, crashing strength and wears resistence of the glass-ceramics ranged from 6.5–7.5, from 2000–6300 kg/cm2 and from 0.1–0.2 g/cm, respectively. Keywords: glass-ceramics, microstructure, mechanical properties. REFERENCES 1. G. Beall, H. Rittler, Am. Ceram. Bull. 55 (1976) 579 2. H. Kim, J. So, J. Ceram. Pro. Res. 1 (2000) 96 3. S. Chang, H. Jung, J. Korean Ceram. Soc. 17 (1980) 151 4. S. Kapur, N. Sakarya, E. Patrick, M. Paglia, Brit. Ceram. Trans. 94 (1995) 33 5. M. Kirsh, G. Berger, U. Banach, T. Hubert, Intercer. 3 (1988) 34 6. G. Kovacs, I. Lazau, I. Menessy, K. Kovacs, Kay Eng. Mat. 132–136 (1997) 2135 7. J. Wiliamson, J. Tipple, S. Rogers, J. Iron and Steel Ind. 206 (1968) 898 8. M. Ovecoglu, B. Kuban, H. Ozer, J. Europ. Ceram. Soc. 17 (1997) 957. J.Serb.Chem.Soc. 68(6)511–513(2003) UDC 669.3–492.2/.3+621.357:532.14 JSCS – 3067 Preliminary communication PRELIMINARY COMMUNICATION The critical apparent density for the free flow of copper powder KONSTANTIN I. POPOV1, SNE@ANA B. KRSTI]1 and MIOMIR G. PAVLOVI]2 1Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, 11000 Belgrade and ICTM–Center for Electrochemistry, Njego{eva 12, 11000 Belgrade, Serbia and Montenegro (Received 26 December 2002) Abstract: A method for the determination of the critical apparent density, which permits the free flow of electrodeposited copper powder is discussed. It was found that powders the apparent density of which were larger than 2.3 g/cm3 exhibit free flow. This is in good agreement with the literature data. Keywords: copper powder flowability, critical apparent density for free flow. REFERENCES 1. K. I. Popov, N. D. Nikoli}, Z. Rako~evi}, J. Serb. Chem. Soc. 67 (2002) 861 2. A. Calusaru, Electrodeposition of Metal Powders, Elsevier, Amsterdam-Oxford-New York, 1979, p. 296 3. E. Peisseker, J. of Powder Metallurgy and Powder Technology 20 (1984) 27 4. M. G. Pavlovi}, Lj. J. Pavlovi}, E. R. Ivanovi}, V. Radmilovi}, K. I. Popov, J. Serb. Chem. Soc. 66 (2001) 923 5. K. I. Popov, Lj. J. Pavlovi}, E. R. Ivanovi}, V. Radmilovi}, M. G. Pavlovi}, J. Serb. Chem. Soc. 67 (2002) 61.