JSCS Vol 67, No. 11  

Adobe Acrobat version

These articles were created using Adobe Acrobat and some were compressed using WinZip

To download the latest
Adobe Acrobat viewer click here


To download the text of the whole issue click here http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif(953 KB - WinZip file)

Impresum http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif44 KB;  Content of Vol 67, No. 8-9 http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif27 KB;  Instruction for authors http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif37 KB


J.Serb.Chem.Soc. 67(11)709–718(2002) 
UDC 667.281.1:678.675:677.027.6
JSCS–2993 
Original scientific paper

To download this article click here 99 KB http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif

Monoazo disperse dyes based on 2-amino-1,3,4-thiadiazole derivatives

HARI R. MARADIYA

V. P. and R. P. T. P. Science College, Vallabh Vidyanagar 388 120, Gujarat State, India

(Received 20 November 2001, revised 27 July 2002)
A series of monoazo disperse dyes based on 2-amino-5-mercapto-1,3,4-thiadiazole was prepared by coupling with various N-arylmaleimides. The dyeing performance of these dyes was assessed on nylon fabric. The dyes were found to give yellow to brown colour shades on dyeing with good depth and levelness on nylon fabric. The dyebath exhaustion, fixation and fastness properties of the dyes were also determined. The dyed fabric showed moderate to good light fastness and very good to excellent fastness to washing, rubbing, perspiration and sublimation. The IR and visible range spectral properties of the dyes were also determined.

Keywords: 2-amino-5-mercapto-1,3,4-thiadiazole,N-arylmaleimides, disperse dyes, dyeing,fixation, fastness.


J.Serb.Chem.Soc. 67(11)719–726(2002) 
UDC 667.28+547.856+542.913:677.494
JSCS–2994
Original scientific paper

To download this article click here 100 KB  http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif

Disperse dyes based on 2-methyl-3-[3’-aminophthalimido]-4(3H)-quinazolinone

VIJAYH. PATEL, MANISH P. PATEL and RANJAN G. PATEL

Department of Chemistry, Sardar Patel University, Vallabh Vidyanagar-388 120, Gujarat, India

(Received 10 January, revised 27 July 2002)
A series of new heterocyclic disperse dyes has been prepared by subsequent diazotization of 2-methyl-3-[3’-aminophthalimido]-4(3H)-quinazolinone and coupling with various mono- and di-N-substituted derivatives of aniline. All the disperse dyes were characterized by their percentage yield, melting point,UV-visible spectrum, elemental analysis, infrared spectrum and dyeing performance on nylon 66 and polyester fibres. The percentage dye bath exhaustion on different fibres was found to be reasonably good and acceptable. The dyed fibres showed fair to fairly good to good fastness to light and very good to excellent fastness to washing, rubbing, perspiration and sublimation.

Keywords: 3’-aminophthalimido; quinazolinone; synthesis; nylon 66 fibres; polyester fibres; dyeing properties.


J.Serb.Chem.Soc. 67(11)727–734(2002) 
UDC 667.281.004.14+542.913:677.494
JSCS–2995
Original scientific paper

To download this article click here 100 KB  http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif

Synthesis and application of novel heterocyclic dyes based on 11-amino-13H-acenaphtho[1,2-e]pyridazino[3,2-b]quinazolin-13-one

VIJAYH. PATEL, MANISH P. PATEL and RANJAN G. PATEL

Department of Chemistry, Sardar Patel University, Vallabh Vidyanagar-388 120, Gujarat, India

(Received 10 January, revised 26 July 2002)
A new fused heterocyclic compound, 11-amino-13H-acenaphtho[1,2-e]pyridazino [3,2-b]quinazolin-13-one was synthesized and used to prepare a novel series of heterocyclic mono azo dyes by coupling with various naphthols. All the mono azo dyes were characterized by their melting point, elemental analysis,UV-visible spectrum, infrared spectrum and dyeing performance on nylon and polyester fibres. The percentage dye bath exhaustion on different fibres was found to be reasonably good and acceptable. The dyed fibres show fair to good fastness to light and very good to excellent fastness to washing, rubbing, perspiration and sublimation.

Keywords: 11-Amino-13H-acenaphtho[1,2-e]pyridazino[3,2-b]quinazolin-13-one, synthesis, nylon fibres, polyester fibres, dyeing properties.


J.Serb.Chem.Soc. 67(11)735–744(2002) 
UDC 519.87:543.544.1:577.112.385+546.73
JSCS–2996
Original scientific paper

To download this article click here 162 KB  http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif

Computational study of the chromatographic enantioseparation of tris(acetylacetonato)cobalt(III) complexes on an arginine complex of cobalt(III) acting as a chiral selector

LJILJANA CUCKOVIC, ISMET M. HODZIC and SVETOZAR R. NIKETIC*

Chemistry Department, Faculty of Science, University of Belgrade, Studentski trg 16. P. O. Box 158, YU-11001 Belgrade, Yugoslavia and
*Department of Chemistry, University of Fribourg, Pérolles, CH-1700 Fribourg, Switzerland

(Received 28 June 2002)
Acomputational procedure for the modelling of chromatographic separation of neutral tris(acetylacetonato)cobalt(III) into enantiomers on a dinitrobis(arginine)cobalt(III) complex as a chiral selector is described. Predicted elution order calculated from the differences in total energy of interaction for L and D selectands is in agreement with the experimental results. Predictive power of the method and its possible practical applications in designing efficient
chiral stationary phases is demonstrated.

Keywords: Co(III) complexes, chromatographic enantioseparation, molecular mechanics, computational modelling, chirality.


J.Serb.Chem.Soc. 67(11)745–751(2002) 
UDC 66.012+543.344.5:547.56
JSCS – 2997
Original scientific paper

To download this article click here 135 KB  http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif

Factorial design in isocratic high-performance liquid chromatography of phenolic compounds

ANTONIJE ONJIA, TATJANA VASILJEVIC*, DJURO COKESA and MILA LAUSEVIC*

The Vinca Institute of Nuclear Sciences, P. O. Box 522, YU-11001 Belgrade and
*Faculty of Technology and Metallurgy, P. O. Box 494, YU-11001 Beograde, Yugoslavia

A multifactor optimization strategy was utilized to predict the isocratic HPLC separation of nine phenols. The retention behavior was studied as a function of
changing eluent (methanol – acetic acid) composition. The predicted and measured retentions are in rather good agreement. To locate the optimum in the factor space, the normalized resolution product criterion was applied. In virtually every case, the resolution is limited by the separation of the 2-chlorophenol and 2,4-dinitrophenol pair.

Keywords: factorial design, phenols, HPLC, resolution product, isocratic.


J.Serb.Chem.Soc.67(11)753–760(2002) 
UDC 666.32+666.9.022:681.542:66.04
JSCS–2998
Original scientific paper

To download this article click here 87 KB  http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif

The effects of the fine grinding on the physicochemical properties and thermal behavior of bentonite clay

LEPOSAVA FILIPOVIC-PETROVIC, LJILJANA KOSTIC-GVOZDENOVIC* and STANKA ERIC-ANTONI

Zorka-Research Center, Narodnih heroja bb, YU-15000 Sabac and
*Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, YU-11000 Belgrade, Yugoslavia

(Received 20 February, revised 14 August 2002)
In this study, the results obtained by the mechanical treatment of bentonite clay Zavidinci, Serbia in a laboratory vibration mill with rings for different periods of time are presented. The successive structural changes of the minerals were studied by X-ray diffraction analysis, DTA analysis, IR spectroscopy and particle size distribution. The reactivity changes were controlled by CEC. The starting material and the material mechanically treated for 30 min were sintered at several temperature and for different time periods examined by X-ray diffraction. Mechanical treatment by fine grinding of bentonite clay produces structural changes of the powdered material and influences its behavior in further processing steps in particular after thermal treatment.

Keywords: bentonite clay, grinding, properties.


J.Serb.Chem.Soc. 67(11)761–768(2002) 
UDC 546.26-0.33.5+542.943:543.52
JSCS –2999
Original scientific paper

To download this article click here 101 KB http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif

A TPD-MS study of glassy carbon surfaces oxidized by CO2 and O2

ALEKSANDRA A. PERIC-GRUJIC, OLIVERA M. NESKOVIC*, MIOMIR V. VELJKOVIC*, MILA D. LAUSEVIC and ZORAN V. LAUSEVIC*

Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, YU-11000 Belgrade and
*Vinca Institute of Nuclear Sciences, P. O. Box 522, YU-11001 Belgrade, Yugoslavia

(Received 16 May, revised 10 July 2002)
The temperature-programmed desorption (TPD) method combined with mass spectrometric (MS) analysis has been applied to investigate the surface properties of carbon materials. The apparatus consisting of a temperature-programmed furnace and a quadrupole mass spectrometer was constructed in order to characterize the surface of differently treated glassy carbon samples. In this work, samples of glassy carbon exposed to air, CO2 and O2 were examined. The desorption of H2O, CO and CO2, as major products, indicated the presence of different oxide groups. The amount of these groups for all samples was calculated. It is concluded that oxidation affects the nature and the amount of the surface oxide groups and contributes to their increased stability,

Keywords: glassy carbon, oxidation, mass spectra, temperature-programmed desorption.


J.Serb.Chem.Soc. 67(11)769–775(2002) 
UDC 546.56+66.087:546.56'226+532.612
JSCS–3000
Original scientific paper

To download this article click here 82 KB http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif

The estimation of solid copper surface tension in copper sulfate solutions

K. I. POPOV, N. D. NIKOLIC* and Z. RAKOCEVIC**

Faculty of Technology and Metallurgy, Karnegijeva 4, Belgrade,
*ICTM-Institute of Electrochemistry, Njegoseva 12, Belgrade and
**Vinca Institute of Nuclear Sciences, Belgrade, Yugoslavia

(Received 1 July 2002)
In metal electrodeposition in the limiting diffusion current density range, the deposition current density remains constant regardless of the deposition overpotential used. At the same time, the larger the deposition overpotential is the more disperse is the formed deposit, which is characterised by an increased specific surface. The difference in the specific surface of disperse deposits obtained at two different overpotentials in the limiting diffusion current density range is correlated with the difference between the deposition overpotentials.Amethod for the estimation of the surface tension of solid copper in copper sulfate solutions is also proposed.

Keywords: interfacial energy copper-copper sulfate solution, specific surface of copper powder.


J.Serb.Chem.Soc. 67(11)777–782(2002) 
UDC 546.76+546.226–325+541.8:620.123.4
JSCS–3001
Preliminary communication

To download this article click here 74 KB http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif

PRELIMINARY COMMUNICATION
Dissolution of chromium in sulfuric acid

D. M. DRAZIC and J. P. POPIC

Institute of Chemistry, Technology and Metallurgy - Center for Electrochemistry, Njegoseva 12, P. O. Box 815, YU-11001 Belgrade, Yugoslavia

(Received 8 August 2002)
By combining electrochemical corrosion rate measurements and spectrophotometric analysis of the electrolyte it was shown that at room temperature chromium dissolves in deaerated 0.1 M Na2SO4 + H2SO4 (pH 1) solution as Cr(II) and Cr(III) ions in he ratio Cr(II) : Cr(III) @ 7 : 1. This process was stable over 4 h without any detectable change. The total corrosion rate of chromium calculated from the analytical data is about 12 times higher, than that determined electrochemically by cathodic Tafel line extrapolation to the corrosion potential. This finding was confirmed by applying the weight-loss method for the determination of the corrosion rate. This enormous difference between these experimentally determined corrosion rates can be explained by the rather fast, “anomalous” dissolution process proposed by Kolotyrkin and coworkers (chemical reaction of Cr with H2O molecules) occurring simultaneously with the electrochemical corrosion process.

Keywords: chromium, corrosion, acid solutions, corrosion products, anomalous dissolution.


J.Serb.Chem.Soc. 67(11)783–792(2002) 
UDC 577.112.385+543.23:615
JESCS–3002
Original scientific paper

To download this article click here 104 KB http://www.shd.org.rs/HtDocs/SHD/PDFicon.gif

A kinetic determination of lysine in pharmaceutical sample

S. S. MITIC, G. Z. MILETIC, A. N. PETROVIC and S. B. TOSIC

Faculty of Sciences and Mathematics, Department of Chemistry, University of Nis, Visegradska 33, P. O. Box 224, YU-18000 Nis, Yugoslavia

(Received 17 May, revised 16 June 2002)
Akinetic method for the determination of micro quantities of the amino acid lysine (Lys) is described in this paper. The catalytic activity of cobalt in the reaction of the oxidation of purpurin (1,2,4-trihydroxyanthraquinone, PP) by hydrogen peroxide in alkaline buffer solution decreases in the presence of micro quantities of lysine, because of the formation of a complex. The experimental conditions for the successful determination of lysine were optimized. The relative error ranges from 7.7 to 1.9% in the concentration range from 0.118 to 23.520 mg cm-3. The detection limit is 0.023 mg cm-3. Kinetic equations are proposed for the investigated process. The effects of certain foreign ions and amino acids on the reaction rate were determined in order to assess the selectivity of the method. The method was applied to the determination of lysine in a pharmaceutical sample Riborn-P (Medecon–Belgrade).

Keywords: kinetic method, lysine, purpurin oxidation, pharmaceutical sample.


Society Home Page

Contents of this Vol.

Journal Home Page

Copyright & copy; SHD 2002.
Last Updated November 29, 2002.
For more information contact: SHD@elab.tmf.bg.ac.yu