Tsveta Stanimirova

Prof. Tsveta Stanimirova

Sofia University, Sofia, Sofia-Grad, Bulgaria
orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 1999 in Journal of Materials Science
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Journal Article
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TSTsveta Stanimirova
Tsveta Stanimirova
IVI. Vergilov
I. Vergilov
GKG. Kirov
G. Kirov
NPNadia Lubomirova Petrova
Nadia Lubomirova Petrova

1 February 2001 in Journal of Materials Science Letters
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Journal Article
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TSTsveta Stanimirova
Tsveta Stanimirova
GKG. Kirov
G. Kirov
EDE. Dinolova
E. Dinolova

1 June 2004 in Clay Minerals
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Journal Article
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TSTsveta Stanimirova
Tsveta Stanimirova
NPN. Piperov
N. Piperov
NPNadia Lubomirova Petrova
Nadia Lubomirova Petrova
GKG. Kirov
G. Kirov
The thermal decomposition of hydrotalcite (HT), with chemical composition Mg1-xAlx(OH)2(CO3)x/2.(1-3x/2)H2O, (0.20 < x ≤ 0.33), is a complex sequence of dehydration, dehydroxylation and decarbonization and leads to the formation of a series of metaphases: HT-D (dehydrated HT), HT-B (partially dehydroxylated HT) and MO (mixed oxides with periclase-like structure). The evolution of water and CO2 in natural and synthetic hydrotalcites (a Mg/Al ratio between 2:1and 3.7:1), heated to 800°C, was investigated by differential thermal analysis, thermogravimetry and evolved gas analysis. At least six endothermic and two exothermic effects were established by computer-aided resolving of the curves. The formation of each HT metaphase was related to the release of a discrete number of water molecules depending on the Al content in the samples and each appeared as a corresponding endothermic peak in the DTA curves. The exothermic processes associated with the crystallization of HT-B and MO metaphases were specified by decomposition of DTA curves. The evolution of CO2 during the thermal decomposition of the carbonate groups was found to be different for the samples studied. The preservation of CO3 even at high temperatures was established for synthetic samples with a high Al content. The release of volatile H2O and CO2 (which comprise ~40% of the sample mass) provokes fine cracking both along and across the layers.

23 February 2016 in Journal of Thermal Analysis and Calorimetry
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Journal Article
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TSTsveta Stanimirova
Tsveta Stanimirova
NPNadia Lubomirova Petrova
Nadia Lubomirova Petrova
GKGeorgi Kirov
Georgi Kirov

14 November 2008 in Journal of Thermal Analysis and Calorimetry
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Journal Article
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TSTsveta Stanimirova
Tsveta Stanimirova
VBV. Balek
V. Balek

1 June 2011 in Clay Minerals
Verified
Journal Article
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GKG. Kirov
G. Kirov
EŠE. Šamajova
E. Šamajova
RNR. Nedialkov
R. Nedialkov
TSTsveta Stanimirova
Tsveta Stanimirova
The genesis of the products of the alteration of acid pyroclastic material is discussed and interpreted on the basis of the distribution, sedimentation conditions, post-sedimentation activity, mineral and chemical compositions of pyroclastic deposits in Bulgaria and Slovakia.It is found that the disordered nonequilibrium nature of the volcanic glass induces a diagenetic devitrification of the tuffs and formation of clinoptilolitic, adularia-cristobalite and bentonite rocks. With increasing temperature, the volcanic glass tends forward a stable state through a series of zeolite mineral associations: clinoptilolite-mordenite-analcime-feldspar. The change in mineral composition of this series of rocks occurs without a change in the chemical composition of the rocks, which could be explained by the closed nature of zeolite systems. The formation of bentonites is associated with the removal of alkaline ions under diagenetic conditions, while the formation of halloysite rocks is caused by hydrothermal activity.