Šipka, V.

Link to this page

Authority KeyName Variants
529fb401-cf37-4ecb-bfd2-8ea87fad27ff
  • Šipka, V. (5)
Projects
No records found.

Author's Bibliography

Long lived radionuclides in the ecosystem of the Sava river

Vuković, Živorad; Šipka, V.; Todorović, Dragana; Stanković, Srboljub

(2006)

TY  - JOUR
AU  - Vuković, Živorad
AU  - Šipka, V.
AU  - Todorović, Dragana
AU  - Stanković, Srboljub
PY  - 2006
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2989
AB  - The radioactivity of water and sediments from the Sava river in the course through Serbia during 2001-2003 has been examined by alpha- and gamma-ray spectrometry. Except for cesium originating from Chernobyl, the radioactivity level of water and sediment coincide with the content of natural radionuclides in the environment of the river basin. Distribution coefficients as well as the runoff coefficient were determined for (137)pCs.
T2  - Journal of Radioanalytical and Nuclear Chemistry
T1  - Long lived radionuclides in the ecosystem of the Sava river
VL  - 268
IS  - 1
SP  - 129
EP  - 131
DO  - 10.1556/JRNC.268.2006.1.21
ER  - 
@article{
author = "Vuković, Živorad and Šipka, V. and Todorović, Dragana and Stanković, Srboljub",
year = "2006",
abstract = "The radioactivity of water and sediments from the Sava river in the course through Serbia during 2001-2003 has been examined by alpha- and gamma-ray spectrometry. Except for cesium originating from Chernobyl, the radioactivity level of water and sediment coincide with the content of natural radionuclides in the environment of the river basin. Distribution coefficients as well as the runoff coefficient were determined for (137)pCs.",
journal = "Journal of Radioanalytical and Nuclear Chemistry",
title = "Long lived radionuclides in the ecosystem of the Sava river",
volume = "268",
number = "1",
pages = "129-131",
doi = "10.1556/JRNC.268.2006.1.21"
}
Vuković, Ž., Šipka, V., Todorović, D.,& Stanković, S.. (2006). Long lived radionuclides in the ecosystem of the Sava river. in Journal of Radioanalytical and Nuclear Chemistry, 268(1), 129-131.
https://doi.org/10.1556/JRNC.268.2006.1.21
Vuković Ž, Šipka V, Todorović D, Stanković S. Long lived radionuclides in the ecosystem of the Sava river. in Journal of Radioanalytical and Nuclear Chemistry. 2006;268(1):129-131.
doi:10.1556/JRNC.268.2006.1.21 .
Vuković, Živorad, Šipka, V., Todorović, Dragana, Stanković, Srboljub, "Long lived radionuclides in the ecosystem of the Sava river" in Journal of Radioanalytical and Nuclear Chemistry, 268, no. 1 (2006):129-131,
https://doi.org/10.1556/JRNC.268.2006.1.21 . .
3

Hypervalent molecular cluster: C28H4

Veljković, Miomir V.; Nešković, Olivera M.; Deric, A; Veličković, Suzana; Šipka, V.

(2005)

TY  - JOUR
AU  - Veljković, Miomir V.
AU  - Nešković, Olivera M.
AU  - Deric, A
AU  - Veličković, Suzana
AU  - Šipka, V.
PY  - 2005
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6525
AB  - A growing number of recent publications on clusters reflect a tremendous interest in these particles. These studies reveal new fundamental physical and chemical aspects of matter. Clusters are called the fifth state of matter: liquid, solid, cluster, gas and plasma. In this work, a carbon cluster was generated by a spark cluster source and detected by single focusing mass spectrometer in situ. We examined the effects of cluster source parameters on the generation of carbon cluster and report our initial results. This method should be useful for studying the mechanism of fullerene formation. In the case when carbon clusters generated in plasma arc are carried by the Ar or H-2 gas flow downstream through a vacuum chamber to the ion source of mass spectrometer, we obtained a small binary carbon cluster C28H4 (hydrogenated fullerene). The empty fullerene is tetravalent and strongly binds four hydrogen atoms, which significantly weakens two different sets of bonds and leads to an open-shell electronic structure. Conclusion is that endohedral C28H4 are hypervalent. We have demonstrated how in situ mass spectrometry has led to the rapid development of an important branch of synthetic fullerene chemistry that has yielded many new small fullerenes and related derivatives with novel structures and properties. The impact of mass spectrometry on the synthesis of fullerene derivatives is the subject of this paper. Significantly, a large fraction of products could be condensed on a specially designed collection plate, which allows further spectroscopic characterization of new derivatives.
T2  - Materials Science Forum
T1  - Hypervalent molecular cluster: C28H4
VL  - 494
SP  - 181
EP  - 186
DO  - 10.4028/www.scientific.net/MSF.494.181
ER  - 
@article{
author = "Veljković, Miomir V. and Nešković, Olivera M. and Deric, A and Veličković, Suzana and Šipka, V.",
year = "2005",
abstract = "A growing number of recent publications on clusters reflect a tremendous interest in these particles. These studies reveal new fundamental physical and chemical aspects of matter. Clusters are called the fifth state of matter: liquid, solid, cluster, gas and plasma. In this work, a carbon cluster was generated by a spark cluster source and detected by single focusing mass spectrometer in situ. We examined the effects of cluster source parameters on the generation of carbon cluster and report our initial results. This method should be useful for studying the mechanism of fullerene formation. In the case when carbon clusters generated in plasma arc are carried by the Ar or H-2 gas flow downstream through a vacuum chamber to the ion source of mass spectrometer, we obtained a small binary carbon cluster C28H4 (hydrogenated fullerene). The empty fullerene is tetravalent and strongly binds four hydrogen atoms, which significantly weakens two different sets of bonds and leads to an open-shell electronic structure. Conclusion is that endohedral C28H4 are hypervalent. We have demonstrated how in situ mass spectrometry has led to the rapid development of an important branch of synthetic fullerene chemistry that has yielded many new small fullerenes and related derivatives with novel structures and properties. The impact of mass spectrometry on the synthesis of fullerene derivatives is the subject of this paper. Significantly, a large fraction of products could be condensed on a specially designed collection plate, which allows further spectroscopic characterization of new derivatives.",
journal = "Materials Science Forum",
title = "Hypervalent molecular cluster: C28H4",
volume = "494",
pages = "181-186",
doi = "10.4028/www.scientific.net/MSF.494.181"
}
Veljković, M. V., Nešković, O. M., Deric, A., Veličković, S.,& Šipka, V.. (2005). Hypervalent molecular cluster: C28H4. in Materials Science Forum, 494, 181-186.
https://doi.org/10.4028/www.scientific.net/MSF.494.181
Veljković MV, Nešković OM, Deric A, Veličković S, Šipka V. Hypervalent molecular cluster: C28H4. in Materials Science Forum. 2005;494:181-186.
doi:10.4028/www.scientific.net/MSF.494.181 .
Veljković, Miomir V., Nešković, Olivera M., Deric, A, Veličković, Suzana, Šipka, V., "Hypervalent molecular cluster: C28H4" in Materials Science Forum, 494 (2005):181-186,
https://doi.org/10.4028/www.scientific.net/MSF.494.181 . .
2
1

Carbon nanotubes as assisted matrix for fullerenes

Šipka, V.; Nešković, Olivera M.; Veljković, Miomir V.; Veličković, Suzana

(2005)

TY  - JOUR
AU  - Šipka, V.
AU  - Nešković, Olivera M.
AU  - Veljković, Miomir V.
AU  - Veličković, Suzana
PY  - 2005
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6526
AB  - Matrix-assisted laser desorption/ionization (MALDI) coupled with reflectron time-off-light mass spectrometry was applied to the analysis of fullerenes (C-60 and C-70). This investigation included the screening of three different compounds regarding their suitability as MALDI matrices. It has been found that the performance of alpha-cyano-4-hydroxycinnamic acid (CHCA), currently one of the most universally used matrices in MALDI analyses, is exceeded by some of these materials. In the negative ion-mode, excellent performance has been achieved using 2-[(2E)-3-(4-tertbutylphenyl)-2-methylprop-2-enylidene] malonitrile (DCTB). These matrixes should efficiently absorb at commonly used laser wavelength (typically for a 337-nm nitrogen laser) and form homogeneous microcrystalline solids with analyte molecules. The soft ionization technique affords little to no fragmentation of analyte. Carbon nanotubes, prepared by an are discharge method, were investigated as the third matrix. It was observed that the carbon nanotube layer as a matrix provides high detection sensitivity and mass resolution of fullerenes with eliminating matrix ion interference.
T2  - Materials Science Forum
T1  - Carbon nanotubes as assisted matrix for fullerenes
VL  - 494
SP  - 187
EP  - 192
UR  - https://hdl.handle.net/21.15107/rcub_vinar_6526
ER  - 
@article{
author = "Šipka, V. and Nešković, Olivera M. and Veljković, Miomir V. and Veličković, Suzana",
year = "2005",
abstract = "Matrix-assisted laser desorption/ionization (MALDI) coupled with reflectron time-off-light mass spectrometry was applied to the analysis of fullerenes (C-60 and C-70). This investigation included the screening of three different compounds regarding their suitability as MALDI matrices. It has been found that the performance of alpha-cyano-4-hydroxycinnamic acid (CHCA), currently one of the most universally used matrices in MALDI analyses, is exceeded by some of these materials. In the negative ion-mode, excellent performance has been achieved using 2-[(2E)-3-(4-tertbutylphenyl)-2-methylprop-2-enylidene] malonitrile (DCTB). These matrixes should efficiently absorb at commonly used laser wavelength (typically for a 337-nm nitrogen laser) and form homogeneous microcrystalline solids with analyte molecules. The soft ionization technique affords little to no fragmentation of analyte. Carbon nanotubes, prepared by an are discharge method, were investigated as the third matrix. It was observed that the carbon nanotube layer as a matrix provides high detection sensitivity and mass resolution of fullerenes with eliminating matrix ion interference.",
journal = "Materials Science Forum",
title = "Carbon nanotubes as assisted matrix for fullerenes",
volume = "494",
pages = "187-192",
url = "https://hdl.handle.net/21.15107/rcub_vinar_6526"
}
Šipka, V., Nešković, O. M., Veljković, M. V.,& Veličković, S.. (2005). Carbon nanotubes as assisted matrix for fullerenes. in Materials Science Forum, 494, 187-192.
https://hdl.handle.net/21.15107/rcub_vinar_6526
Šipka V, Nešković OM, Veljković MV, Veličković S. Carbon nanotubes as assisted matrix for fullerenes. in Materials Science Forum. 2005;494:187-192.
https://hdl.handle.net/21.15107/rcub_vinar_6526 .
Šipka, V., Nešković, Olivera M., Veljković, Miomir V., Veličković, Suzana, "Carbon nanotubes as assisted matrix for fullerenes" in Materials Science Forum, 494 (2005):187-192,
https://hdl.handle.net/21.15107/rcub_vinar_6526 .

Tritium around the Vinca Institute of Nuclear Sciences

Miljević, Nada R.; Šipka, V.; Žujić, Aleksandra; Golobočanin, Dušan D.

(2000)

TY  - JOUR
AU  - Miljević, Nada R.
AU  - Šipka, V.
AU  - Žujić, Aleksandra
AU  - Golobočanin, Dušan D.
PY  - 2000
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2331
AB  - The spatial and temporal distributions of tritium in precipitation, river water, atmospheric water vapor, and air were observed in the Belgrade area over the period 1988-1997. Significantly higher tritium levels were measured in samples in the vicinity of the Vinca Institute of Nuclear Sciences compared with off-site locations. Annual mean tritium concentrations in precipitation ranged from 2.2 to 35.4 Bq/1, decreasing with distance from the nuclear facilities. The annual mean release of tritium into the environment from heavy water reactor operations at the Vinca Institute based on precipitation measurements was estimated to be about 80 TBq. Data show a large variability of tritium concentration in the air, fluctuating in the ranges 0.27-60.8 Bq/m(3) air (16-2468 Bq/l-H2O) in atmospheric water vapor in which tritium occurs as HTO and 0.04-1.05 Bq/m(3) air hue to the tritium content in atmospheric hydrogen gas. Annual average concentrations observed for HTO and HT forms were 11.5-19.1 and 0.46-0.48 Bq/m(3) air respectively. The two data sets for HTO and HT are similar, suggesting a near steady state over the period of observation. (C) 2000 Elsevier Science Ltd. All rights reserved.
T2  - Journal of Environmental Radioactivity
T1  - Tritium around the Vinca Institute of Nuclear Sciences
VL  - 48
IS  - 3
SP  - 303
EP  - 315
DO  - 10.1016/S0265-931X(99)00082-X
ER  - 
@article{
author = "Miljević, Nada R. and Šipka, V. and Žujić, Aleksandra and Golobočanin, Dušan D.",
year = "2000",
abstract = "The spatial and temporal distributions of tritium in precipitation, river water, atmospheric water vapor, and air were observed in the Belgrade area over the period 1988-1997. Significantly higher tritium levels were measured in samples in the vicinity of the Vinca Institute of Nuclear Sciences compared with off-site locations. Annual mean tritium concentrations in precipitation ranged from 2.2 to 35.4 Bq/1, decreasing with distance from the nuclear facilities. The annual mean release of tritium into the environment from heavy water reactor operations at the Vinca Institute based on precipitation measurements was estimated to be about 80 TBq. Data show a large variability of tritium concentration in the air, fluctuating in the ranges 0.27-60.8 Bq/m(3) air (16-2468 Bq/l-H2O) in atmospheric water vapor in which tritium occurs as HTO and 0.04-1.05 Bq/m(3) air hue to the tritium content in atmospheric hydrogen gas. Annual average concentrations observed for HTO and HT forms were 11.5-19.1 and 0.46-0.48 Bq/m(3) air respectively. The two data sets for HTO and HT are similar, suggesting a near steady state over the period of observation. (C) 2000 Elsevier Science Ltd. All rights reserved.",
journal = "Journal of Environmental Radioactivity",
title = "Tritium around the Vinca Institute of Nuclear Sciences",
volume = "48",
number = "3",
pages = "303-315",
doi = "10.1016/S0265-931X(99)00082-X"
}
Miljević, N. R., Šipka, V., Žujić, A.,& Golobočanin, D. D.. (2000). Tritium around the Vinca Institute of Nuclear Sciences. in Journal of Environmental Radioactivity, 48(3), 303-315.
https://doi.org/10.1016/S0265-931X(99)00082-X
Miljević NR, Šipka V, Žujić A, Golobočanin DD. Tritium around the Vinca Institute of Nuclear Sciences. in Journal of Environmental Radioactivity. 2000;48(3):303-315.
doi:10.1016/S0265-931X(99)00082-X .
Miljević, Nada R., Šipka, V., Žujić, Aleksandra, Golobočanin, Dušan D., "Tritium around the Vinca Institute of Nuclear Sciences" in Journal of Environmental Radioactivity, 48, no. 3 (2000):303-315,
https://doi.org/10.1016/S0265-931X(99)00082-X . .
24
18
22

Ion-exchange separation of uranium, thorium and plutonium isotopes from environmental samples

Radenković, Mirjana; Vuković, Dubravka Ž.; Šipka, V.; Todorović, Dragana

(1996)

TY  - JOUR
AU  - Radenković, Mirjana
AU  - Vuković, Dubravka Ž.
AU  - Šipka, V.
AU  - Todorović, Dragana
PY  - 1996
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7229
AB  - Radioisotopes of uranium, thorium and plutonium in water, soil and fertilizer samples, have been chemically separated and determined by alpha-spectrometry method. Radiochemical Procedure involving ion-exchange, enabled to determine these isotopes in very tow concentrations (under 50 mu Bg/g). U-232, Th-229 and Pu-238 were used as a tracers for radiochemical yield recoveries (up to 90%). Thin layer sources have been obtained by electrodeposition.
T2  - Journal of Radioanalytical and Nuclear Chemistry
T1  - Ion-exchange separation of uranium, thorium and plutonium isotopes from environmental samples
VL  - 208
IS  - 2
SP  - 467
EP  - 475
DO  - 10.1007/BF02040064
ER  - 
@article{
author = "Radenković, Mirjana and Vuković, Dubravka Ž. and Šipka, V. and Todorović, Dragana",
year = "1996",
abstract = "Radioisotopes of uranium, thorium and plutonium in water, soil and fertilizer samples, have been chemically separated and determined by alpha-spectrometry method. Radiochemical Procedure involving ion-exchange, enabled to determine these isotopes in very tow concentrations (under 50 mu Bg/g). U-232, Th-229 and Pu-238 were used as a tracers for radiochemical yield recoveries (up to 90%). Thin layer sources have been obtained by electrodeposition.",
journal = "Journal of Radioanalytical and Nuclear Chemistry",
title = "Ion-exchange separation of uranium, thorium and plutonium isotopes from environmental samples",
volume = "208",
number = "2",
pages = "467-475",
doi = "10.1007/BF02040064"
}
Radenković, M., Vuković, D. Ž., Šipka, V.,& Todorović, D.. (1996). Ion-exchange separation of uranium, thorium and plutonium isotopes from environmental samples. in Journal of Radioanalytical and Nuclear Chemistry, 208(2), 467-475.
https://doi.org/10.1007/BF02040064
Radenković M, Vuković DŽ, Šipka V, Todorović D. Ion-exchange separation of uranium, thorium and plutonium isotopes from environmental samples. in Journal of Radioanalytical and Nuclear Chemistry. 1996;208(2):467-475.
doi:10.1007/BF02040064 .
Radenković, Mirjana, Vuković, Dubravka Ž., Šipka, V., Todorović, Dragana, "Ion-exchange separation of uranium, thorium and plutonium isotopes from environmental samples" in Journal of Radioanalytical and Nuclear Chemistry, 208, no. 2 (1996):467-475,
https://doi.org/10.1007/BF02040064 . .
10
6
10