Kestutis Joksas

Dr. Kestutis Joksas

Geoenvironmental research laboratory, Nature Research Centre, Vilnius, Vilniaus Miestas, Lithuania
orcid

Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

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

Representative Publications

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19 November 2022 in Molecules
Verified
Journal Article
Open access
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GLGalina Lujanienė
Galina Lujanienė
RNRaman Novikau
Raman Novikau
EJEdith Flora Joel
Edith Flora Joel
KKKarolina Karalevičiūtė
Karolina Karalevičiūtė
SŠSergej Šemčuk
Sergej Šemčuk
KJKestutis Joksas
Kestutis Joksas
The adsorption of Eu(III) on composites synthesised from graphene oxide (GO), maghemite (MGH), and chitosan (CS) has been studied using different approaches. The physicochemical and morphological characteristics of the composites GO-MGH, GO-CS, GO-MGH-CS I, II, and III were determined by XRD, Mössbauer spectroscopy, FTIR, Raman spectroscopy, and TEM. According to the results of batch experiments, the maximum experimental adsorption capacity was 52, 54, 25, 103, and 102 mg/g for GO-MGH, GO-CS, GO-MGH-CS I, II, and III, respectively. The data obtained are in better agreement with the Langmuir, pseudo-second-order, and pseudo-first-order models only for GO-MGH. Thus, the adsorption of Eu(III) on the composites was a favourable, monolayer, and occurred at homogeneous sites. The nature of adsorption is chemical and, in the case of GO-MGH, physical. Tests of the composites in natural waters showed a high removal efficiency for Eu(III), Pu(IV), and Am(III), ranging from 74 to 100%. The ANFIS model has quite good predictive ability, as shown by the values for R2, MSE, SSE, and ARE. The GO-MGH-CS composites with the high adsorption capacity could be promising candidates for the removal of Eu(III) and the pre-concentration of Pu(IV) and Am(III) from natural waters.

26 November 2023 in Water
Verified
Journal Article
Open access
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RSRimutė Stakėnienė
Rimutė Stakėnienė
KJKestutis Joksas
Kestutis Joksas
Jūratė KriaučiūnienėJūratė Kriaučiūnienė
Jūratė Kriaučiūnienė
Darius JakimavičiusDarius Jakimavičius
Darius Jakimavičius
Eva Raudonytė-SvirbutavičienėEva Raudonytė-Svirbutavičienė
Eva Raudonytė-Svirbutavičienė
The Baltic Sea faces prolonged eutrophication due to nutrient pollution, with the Nemunas River regulating nutrient input via the Curonian Lagoon. In this study, we aimed to assess the seasonal variations and changes over the past two decades in nutrient concentrations within the Curonian Lagoon–Baltic Sea transitional zone, and to identify the main factors affecting these trends. We observed slightly reduced nutrient levels in the lagoon and the Klaipėda Strait and increased nitrogen loadings in the Baltic Sea nearshore over time. Between 2007 and 2009, the average total nitrogen (TN) concentrations in the Klaipeda Strait and the Baltic Sea were 1.60 ± 0.25 and 0.54 ± 0.04 mg/L, respectively, while the average total phosphorus (TP) concentrations in the Klaipeda Strait and the Baltic Sea were 0.061 ± 0.04 and 0.03 ± 0.01 mg/L, respectively. Between 2018 and 2020, TN concentrations in the Strait and the Sea were 1.2 ± 0.36 and 0.65 ± 0.32 mg/L, respectively, while the average TP concentrations in the Klaipeda Strait and the Baltic Sea were 0.025 ± 0.002 and 0.021 ± 0.002 mg/L, respectively. The average annual amount of TN and TP entering the Curonian Lagoon from the sea was 2736 t and 162 t, respectively. Significantly higher nutrient influx to the Baltic Sea was recorded reaching 32,302 t for TN and 1278 t for TP. Nutrient concentrations correlated with water temperature, salinity, and dissolved oxygen, influenced by seasonal runoff patterns and climate change. Over time, there have been noticeable shifts in environmental conditions, including rising temperatures, decreasing oxygen levels, salinity changes, increased evaporation, and reduced precipitation.

4 August 2023 in Environmental Pollution
Verified
Journal Article
Closed access
Eva Raudonytė-SvirbutavičienėEva Raudonytė-Svirbutavičienė
Eva Raudonytė-Svirbutavičienė
KJKestutis Joksas
Kestutis Joksas
RSRimutė Stakėnienė
Rimutė Stakėnienė
ARAleksandras Rybakovas
Aleksandras Rybakovas
RNReda Nalivaikienė
Reda Nalivaikienė
KAKestutis Arbaciauskas
Kestutis Arbaciauskas

30 September 2019 in Environmental and Molecular Mutagenesis
Verified
Journal Article
Closed access
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ARAleksandras Rybakovas
Aleksandras Rybakovas
KAKestutis Arbaciauskas
Kestutis Arbaciauskas
VMVaida Markovskienė
Vaida Markovskienė
KJKestutis Joksas
Kestutis Joksas

25 March 2026 in Nanomaterials
Verified
Journal Article
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SŠSergej Šemčuk
Sergej Šemčuk
ŽJŽivilė Jurgelėnė
Živilė Jurgelėnė
VPVidas Pakštas
Vidas Pakštas
DMDanguolė Montvydienė
Danguolė Montvydienė
ADAudrius Drabavicius
Audrius Drabavicius
GLGalina Lujanienė
Galina Lujanienė
Biopolymers such as chitosan are considered important candidates for water purification due to their non-toxicity, biodegradability, natural origin, biocompatibility, and potential for modification to provide additional capabilities, such as incorporating nanomaterials for magnetism to enable rapid separation or adding functional groups to enhance selectivity towards target adsorbates. This study investigated adsorption of Co (II), traced by Co-60 radionuclide, systematically evaluated in natural aquatic matrices selected according to water body type: seawater (Baltic Sea) and freshwater systems further distinguished as lentic (Lake Balsys) and lotic (Neris River) environments, using synthesized magnetite–chitosan nanocomposites (MCNs) with varying loadings of Fe3O4 (10–30 wt. %) nanoparticles providing different levels of magnetization. Comprehensive characterization (TEM, FTIR, AFM, XRD, and Mössbauer spectroscopy) confirmed successful integration of magnetite nanoparticles within the chitosan matrix and reproducible structural properties. An optimal magnetization of 11 emu/g was achieved at 20 wt. % Fe3O4, enabling rapid magnetic separation within <1 min without compromising sorption capacity. Adsorption isotherm models were applied to investigate the adsorption parameters, and sorption kinetics were studied, yielding a maximum adsorption capacity of 14.93 mg/g for MCN-10 in seawater and 11.95 mg/g for MCN-20 in freshwater with observed equilibrium within 120 min. These promising results indicate that the MCN is a suitable nanocomposite for the removal of Co (II) ions and the Co-60 radionuclide from aquatic media.

1 January 2021 in Baltica
Verified
Journal Article
Open access
Eva Raudonytė-SvirbutavičienėEva Raudonytė-Svirbutavičienė
Eva Raudonytė-Svirbutavičienė
RSRimutė Stakėnienė
Rimutė Stakėnienė
IBIeva Baužienė
Ieva Baužienė
KJKestutis Joksas
Kestutis Joksas
In this study, results on PAHs distribution, origin and ecological risks from several surveys are combined with a special focus on naphthalene. The study area comprises a large part of the Lithuanian territory and includes two biggest Lithuanian rivers, Nemunas and Neris (sampling locations with different hydrodynamics and varying anthropogenic pressure), four different lakes and the central part of the Curonian Lagoon. ∑16PAHs concentrations in the surface sediment ranged between 74.5 and 6377 ng g-1 dw. In 9 locations out of 14, naphthalene concentration exceeded TEL and posed a threat to the environment. Naphthalene was a significant contributor to the total PAHs concentration in the study area with concentrations ranging from 0.78 to 106 ng g-1 dw. Despite the highest naphthalene concentration recorded in Lake Talkša, naphthalene had only a minor contribution to the PAH profile in this lake. Even a lower impact of naphthalene was observed in the Curonian Lagoon. Naphthalene was found to be the prevailing compound in the Nemunas River Delta region, in a relatively clean Lithuanian Lake Dusia and in some Neris River locations. The highest contribution of naphthalene was observed in the areas with low urbanization degree, but close to peatlands. The main naphthalene source in the study area might be related to peatlands, albeit additional naphthalene sources, such as food cooking, burning of agricultural residues, wood and coal could not be completely rejected either. The sources of other PAHs are attributed to the vehicular emission, emissions from industry, biomass and coal burning.