Yalçın, Şerife

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Name Variants
Yalçin, Serife
Yalcin, S.
Yalçin, S.
Yalcin, S
Yalçin, Ş.
Yalcin, Serife
Yalcin, Şerife
Yalçın, Şerife Hanım
Yalçın, Şerife
Yalçın, Ş.
Yalçın, Ş
Yalcin, Serife Hanim
Yalçin, Şerife
Job Title
Email Address
serifeyalcin@iyte.edu.tr
Main Affiliation
04.01. Department of Chemistry
Status
Current Staff
Scopus Author ID
Turkish CoHE Profile ID
Google Scholar ID
WoS Researcher ID

Sustainable Development Goals

NO POVERTY1
NO POVERTY
0
Research Products
ZERO HUNGER2
ZERO HUNGER
0
Research Products
GOOD HEALTH AND WELL-BEING3
GOOD HEALTH AND WELL-BEING
0
Research Products
QUALITY EDUCATION4
QUALITY EDUCATION
0
Research Products
GENDER EQUALITY5
GENDER EQUALITY
0
Research Products
CLEAN WATER AND SANITATION6
CLEAN WATER AND SANITATION
5
Research Products
AFFORDABLE AND CLEAN ENERGY7
AFFORDABLE AND CLEAN ENERGY
6
Research Products
DECENT WORK AND ECONOMIC GROWTH8
DECENT WORK AND ECONOMIC GROWTH
0
Research Products
INDUSTRY, INNOVATION AND INFRASTRUCTURE9
INDUSTRY, INNOVATION AND INFRASTRUCTURE
10
Research Products
REDUCED INEQUALITIES10
REDUCED INEQUALITIES
0
Research Products
SUSTAINABLE CITIES AND COMMUNITIES11
SUSTAINABLE CITIES AND COMMUNITIES
2
Research Products
RESPONSIBLE CONSUMPTION AND PRODUCTION12
RESPONSIBLE CONSUMPTION AND PRODUCTION
3
Research Products
CLIMATE ACTION13
CLIMATE ACTION
8
Research Products
LIFE BELOW WATER14
LIFE BELOW WATER
0
Research Products
LIFE ON LAND15
LIFE ON LAND
0
Research Products
PEACE, JUSTICE AND STRONG INSTITUTIONS16
PEACE, JUSTICE AND STRONG INSTITUTIONS
0
Research Products
PARTNERSHIPS FOR THE GOALS17
PARTNERSHIPS FOR THE GOALS
0
Research Products
Documents

0

Citations

0

h-index

15

Documents

53

Citations

2007

Scholarly Output

27

Articles

14

Views / Downloads

59411/12034

Supervised MSc Theses

8

Supervised PhD Theses

3

WoS Citation Count

303

Scopus Citation Count

310

Patents

0

Projects

6

WoS Citations per Publication

11.22

Scopus Citations per Publication

11.48

Open Access Source

21

Supervised Theses

11

JournalCount
Spectrochimica Acta, Part B: Atomic Spectroscopy6
Talanta2
Journal of Analytical Atomic Spectrometry1
Journal of Architectural Conservation1
Materials and Structures1
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Scopus Quartile Distribution

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Scholarly Output Search Results

Now showing 1 - 10 of 27
  • Master Thesis
    Determination of Cadmium Bound To Whey Proteins by Laser-Induced Breakdown Spectroscopy at Low Pressures
    (2023) Yalçın, Şerife; Yaman, İlayda; Yalçın, Şerife Hanım
    In this thesis study, a dried-droplet LIBS methodology at reduced pressures for determining cadmium in aqueous media and in biological samples has been developed. With the advantage of the signal enhancement effect at reduced pressures, the optimum pressure for Cd detection was determined. Results were justified with the plasma images taken at different pressures. 100 mbar pressure was found as the optimum for most emission lines of Cd. To find the most suitable substrate onto which analyte droplets will be loaded, silicon wafer-based substrates of different coating types and coating thicknesses were studied. Among them, the c-Si substrate was found to show the highest signal enhancement for Cd detection. The performance of the methodology for quantitative analysis of Cd was shown by standard solutions and certified reference water samples. Calibration curves were constructed, and performance characteristics (limit of detection, accuracy, precision) were evaluated. Detection limits in absolute amounts of 6.8 pg and 1.05 pg were obtained at atmospheric and 100 mbar pressures, respectively. The application studies involve the determination of Cd bound to whey proteins. For this purpose, standard protein (BSA) and whey protein extracted from the milk were incubated in standard Cd solutions for several hours and filtered through cut-off filters via centrifugation. The unreacted cadmium in the filtrate and Cd-bound protein in fraction were analyzed separately. It has been shown that dried-droplet LIBS at reduced pressures is a suitable methodology for identifying and determining Cd and Cd bound to proteins with a picogram amount of detection capability.
  • Article
    Citation - WoS: 23
    Citation - Scopus: 22
    Optimization of Chemical and Instrumental Parameters in Hydride Generation Laser-Induced Breakdown Spectrometry for the Determination of Arsenic, Antimony, Lead and Germanium in Aqueous Samples
    (Elsevier Ltd., 2013) Ünal Yeşiller, Semira; Yalçın, Şerife
    A laser induced breakdown spectrometry hyphenated with on-line continuous flow hydride generation sample introduction system, HG-LIBS, has been used for the determination of arsenic, antimony, lead and germanium in aqueous environments. Optimum chemical and instrumental parameters governing chemical hydride generation, laser plasma formation and detection were investigated for each element under argon and nitrogen atmosphere. Arsenic, antimony and germanium have presented strong enhancement in signal strength under argon atmosphere while lead has shown no sensitivity to ambient gas type. Detection limits of 1.1mgL-1, 1.0mgL-1, 1.3mgL-1 and 0.2mgL-1 were obtained for As, Sb, Pb and Ge, respectively. Up to 77 times enhancement in detection limit of Pb were obtained, compared to the result obtained from the direct analysis of liquids by LIBS. Applicability of the technique to real water samples was tested through spiking experiments and recoveries higher than 80% were obtained. Results demonstrate that, HG-LIBS approach is suitable for quantitative analysis of toxic elements and sufficiently fast for real time continuous monitoring in aqueous environments.
  • Master Thesis
    Identification and Detection of Cis-Platin Binding Proteins by Laser Induced Breakdown Spectroscopy
    (Izmir Institute of Technology, 2015) Kaya, İbrahim; Yalçın, Şerife; Yalçın, Şerife Hanım
    In this study, an all-optically designed laser plasma spectroscopic technique for rapid identification and detection of cisplatin-binding proteins on electrophoretic gel spots prior to molecular mass spectrometric analysis is demonstrated. For this purpose, human serum albumin, human apo transferrin and horse heart myoglobin standard proteins and protein extracts from HeLa cancer cells were subjected to; incubation with cis-platin solution for several hours. Then, non-reducing polyacrylamide gel electrophoretic separation was applied. Followed by the visualization of proteins in the gel by Coomassie Brilliant Blue staining technique protein spots on the gel were dried between two cellophane sheets and subjected to laser ablation by highly energetic laser pulses. In addition, prior to nr-SDS-PAGE separation cis-platin binding to standard proteins were monitored by ESI-MS with several measurements made in 24 hours of incubation time. Using a Nd:YAG laser at its second harmonic wavelength, 532nm, 10 Hz frequency and 10 ns pulse duration, a micro-plasma was created on dried gel spots. Resulting plasma emission light was collected with collection lenses and transferred to a spectrograph via fiber optic cable. An intensified charge coupled device (ICCD) detector enabled multielemental analysis of platinum binding protein samples. Platinum binding proteins were recognized from the prominent neutral emission line, Pt (I) at 273.3 nm, in a plasma formed by the focused laser pulses on the gel, just in the center or in the vicinity of the electrophoretic spot. Spectral emission intensity of Pt lines from LIBS data has been optimized with respect to laser energy and detector timing parameters. Optimization of LIBS experimental parameters have been studied on polyacrylamide gels soaked in cis-Pt solution for Pt signal. It has been shown that, LIBS is a suitable method for identifying Pt in proteins, in gel medium, with nanogram levels of detection capability. The technique was applied to HeLa (human cervical cancer cells) cells extract for the detection of Pt-binded HSA after standard addition of known amounts of protein.
  • Article
    Citation - WoS: 29
    Citation - Scopus: 29
    Investigating Silicon Wafer Based Substrates for Dried-Droplet Analysis by Laser-Induced Breakdown Spectroscopy
    (Elsevier Ltd., 2019) Aras, Nadir; Yalçın, Şerife
    This work communicates a critical assessment on the analytical capability of the three silicon wafer-based substrates; crystalline silicon (c-Si), oxide-coated silicon (SiO2-Si), and nitride-coated silicon (Si3N4-Si), for dried-droplet analysis by laser-induced breakdown spectroscopy. The methodology consists of loading, drying and analyzing steps. First, nanoliter volume of droplets are manually loaded onto the substrate and dried at room temperature. Then, the dry residue is subjected to high peak power (1.15 GW/cm(2)) laser pulses focused outside the minimum focal point condition and luminescent plasma is spectroscopically analyzed. Results revealed that nitride-coated substrate exhibits strong enhancements in signal intensity for most emission lines of the analyte species investigated: Cd, Cr, Cu, Mn, and Pb. Surface reflectivity and surface morphology were comparatively investigated to explore enhanced analytical performance of nitride-coated substrates. Experimental conditions were optimized and growth curves for all the elements are found linear with minimum regression constant of 0.96. LOD's of 62 pg Cd, 1.5 pg Cr, 0.5 pg Cu, 2 pg Mn and 11 pg Pb, in absolute amounts, were obtained. The accuracy and precision of the methodology were tested on certified reference water sample (CRM-TMDW), and ICP-multi-element standard sample (ICP-MES). The surface enhancement effect observed on Si3N4 coated substrates has improved the analytical capability of laser-induced breakdown spectroscopy for liquid analysis.
  • Article
    Characterization of Yellow Patina on Stone Surfaces by Instrumental Analysis Including Libs
    (Taylor & Francis, 2022) Badur, Fulya; Aras, Nadir; Yalçın, Şerife; Böke, Hasan
    Yellow patina formed on the stone surfaces of historical buildings, monuments, and archaeological structures due to weathering is considered a value of the building in the conservation of cultural heritage studies. Although yellow patina layers can be easily distinguished on white marble surfaces, it is not possible to distinguish them on the yellow travertine surfaces with the naked eye. It should be taken into account in yellow travertines as well as marble surfaces before conservation treatments of the stone. In this study, mineralogical and chemical compositions and the thicknesses of yellow patina layers formed on yellow travertine and marble surfaces in Aizanoi, Aphrodisias, and Hierapolis archaeological sites in Turkey were analyzed in order to constitute a conservation approach in the archaeological sites. In this respect, XRD, FT-IR, SEM-EDX, and LIBS were used in the determination of compositions and thicknesses of yellow patina. Although LIBS analysis is a more convenient method to investigate patina layers on stone surfaces, this technique is not as well known as the others. Yellow patina layers contained calcium oxalate in the form of whewellite (CaC2O4.H2O). Their thicknesses were between 15 and 100 μm and should be protective against weathering on travertine and marble surfaces. Highlights LIBS analysis seems to be the most convenient micro-destructive method to estimate the thickness of the yellow patina layers on the marble and yellow travertine surfaces. The determination of the thickness of the yellow patina is critical to keep irreversible cleaning interventions, especially for the yellow travertines due to their similar colors. Yellow patina is mainly composed of calcium oxalate with clay minerals and organic compounds.
  • Conference Object
    Citation - WoS: 21
    Citation - Scopus: 21
    Development of a Continuous Flow Hydride Generation Laser-Induced Breakdown Spectroscopic System: Determination of Tin in Aqueous Environments
    (Elsevier Ltd., 2010) Ünal, Semira; Yalçın, Şerife
    The design, construction and optimization studies of a continuous flow hydride generation laser-induced breakdown spectroscopic system, HG-LIBS, for the determination of tin in aqueous environments is presented. Optimization of the Laser Induced Breakdown Spectroscopy (LIBS) signal with respect to carrier gas flow rate, analyte, acid (HCl) and reductant (NaBH4) concentrations and flow rates was performed by using spectral emission intensity from the neutral Sn(I) line at 284.0 nm under atmospheric pressures. With flow rates of 5.0 mL/min for NaBH4 and 2.5 mL/min for HCl, optimum NaBH4 and HCl concentrations were determined as 2.0% (w/v) and 1.0% (v/v), respectively. The hydride generation efficiency of the system was tested for tin hydride, stannane (SnH4), by inductively coupled plasma mass spectrometer (ICP-MS). It was found that higher than 99% of the analyte was released into the gaseous phase. Upon optimization, the minimum detectable Sn concentration was found as 0.3 mg/L in water samples. That corresponds to more than two orders of increase in sensitivity compared to methods that employ common sample introduction techniques in liquids analysis by LIBS. Over 90% recoveries were obtained from spiking experiments with river, tap and drinking water samples. Results illustrate potential use of the continuous flow HG-LIBS system for monitoring of Sn concentrations in aqueous environments. © 2010 Elsevier Ltd. All rights reserved.
  • Article
    Citation - WoS: 17
    Citation - Scopus: 16
    2-D Analysis of Ge Implanted Sio2 Surfaces by Laser-Induced Breakdown Spectroscopy
    (Elsevier Ltd., 2008) Yalçın, Şerife; Örer, Sabiha; Turan, Raşit
    2-D elemental distribution of Ge in silicon oxide substrates with differing implantation doses of between 3 × 1016 cm- 2 and 1.5 × 1017 cm- 2 has been investigated by Laser-Induced Breakdown Spectroscopy (LIBS). Spectral emission intensity has been optimized with respect to time, crater size, ablation depth and laser energy. Atomic Force Microscopy (AFM) and Scanning Electron Microscopy (SEM) coupled with Energy-Dispersive X-Ray Spectroscopy (EDX) have been utilized to obtain crater depth, morphology and elemental composition of the sample material, respectively. LIBS spectral data revealed the possibility of performing 2-D distribution analysis of Ge atoms in silicon oxide substrate. EDX analysis results confirmed that LIBS is capable to detect Ge atoms at concentrations lower than 0.2% (atomic). LIBS as a fast semi-quantitative analysis method with 50 μm lateral and 800 nm depth resolution has been evaluated. Results illustrate the potential use of LIBS for rapid, on-line assessment of the quality of advanced technology materials during the manufacturing process. © 2008 Elsevier B.V. All rights reserved.
  • Article
    Citation - WoS: 2
    Citation - Scopus: 3
    Determination of Arsenic by Hydride Generation—laser-Induced Breakdown Spectroscopy: Characterization of Interelement Interferences
    (Taylor and Francis Ltd., 2018) Bölek, Deniz; Ünal Yeşiller, Semira; Yalçın, Şerife
    In this study, interelement interferences were evaluated for the determination of arsenic in aqueous samples through laser-induced breakdown spectroscopy (LIBS) hyphenated with a hydride generation sample introduction system. Optimum instrumental and chemical parameters were selected and variation in LIBS signal intensity was recorded for As solution in the presence of comparable concentrations of interfering elements. No significant change in the signal intensity of As(I) 228.8 nm line was observed in the presence of alkali/alkali earth metals; however, the presence of hydride-forming elements has shown a noticeable decrease in the line emission strength of arsenic. The least variation in arsenic signal was observed in the presence of Ge, the most volatile of all. However, the signal has decreased to a greater extent in the presence of Sn, Sb, and Pb. The presence of interfering elements on electron temperature and electron number density of arsenic plasma has also been studied. Plasma temperatures calculated using both As and Ar emission lines in the Boltzmann equation were similar, being around 5000 K. The McWhirter criterion for stationary and homogenous plasmas was utilized for the establishment of the local thermodynamic equilibrium under the plasma conditions studied. Applicability of the technique for multielemental analysis of water samples was tested through spiking experiments. Arsenic signal showed 26% decrease in the multielemental mixture solution. LIBS is among a few atomic spectroscopic techniques that facilitate rapid and simultaneous multielemental analysis without extensive sample preparation steps. However, the analytical performance of the technique still requires more serious efforts to compete with other conventional techniques for routine analysis of environmental samples.
  • Master Thesis
    Investigating the Effect of Metallic Nanoparticles Presence on Signal Intensity for Dried-Droplet Analysis by Laser-Induced Plasma Spectroscopy
    (01. Izmir Institute of Technology, 2021) Tetik Karabıyık, Özge; Yalçın, Şerife Hanım
    While solid sample analysis by LIBS is more easy and straightforward, liquid analysis is more troubling. One of the studies aimed at removing the problems in liquid analysis is the Nanoparticle Enhanced LIBS technique. This study aims to investigate the effect of the presence of Ag nanoparticles of different shape and absorption wavelengths on the signal strength of heavy metals Pb and Cr. For that purpose, spherical, prism, and disc-shaped silver nanoparticles with an absorption wavelength in the range of 394-761 nm were used. Among all types of NPs with different sizes and shapes, silver nanoparticles with an absorption maximum at 535 nm were found to enhance LIBS signal intensity of Pb element at 405.8 nm 5-6 times, and that of Cr at 428.9 nm 3-3.5 times. Under optimized conditions, a LOD value of 1,16 and 0.69 ppb were obtained for Pb and Cr, respectively. The applicability of the system for the determination of Pb and Cr in aqueous environments has also been tested on reference water samples. The silver nanoparticle with an maximum absorbance wavelength of 535 nm shows the most improvement in signal. The wavelength of the laser used is very close to the absorbance wavelength of the silver nanoparticle, effectively overlapping it. Thanks to the transmitted laser light, plasmons are formed on the nanoparticle surface. These formed surface plasmons interact with the laser electromagnetic field, resulting in an increase in the signal.
  • Doctoral Thesis
    Conservation Approaches of Patina Formation on Marble and Travertine Surfaces in the Archaeological Sites
    (Izmir Institute of Technology, 2017) Badur, Fulya; Böke, Hasan; Yalçın, Şerife Hanım
    Patina, which is formed on the stone surfaces of historical buildings and monuments as a result of aging, is considered as a value of the building in the conservation of cultural heritage studies. It should be conserved on calcareous stone surfaces whether or not it represents protective characteristics, since it provides information about previous times. Within this respect, the determination of mineralogical composition, and microstructural and chemical characteristics of patina are critical for the conservation decisions. The aim of this study is to determine the characteristics of yellow patina formation on marble and yellow travertine surfaces to constitute a conservation approach in the archaeological sites. In this study, XRD, FT-IR, SEM-EDX, LIBS and TGA were used to determine the characteristics of yellow patina formation on marble and yellow travertine surfaces in Aizanoi, Aphrodisias, Sardes and Hierapolis. Analysis results indicated that yellow patina is mainly composed of calcium oxalate (whewellite or weddelite) minerals. CaO, MgO, Al2O3, SiO2, P2O5, K2O, SO3, FeO and Na2O were observed on the chemical analyses of the same samples. The results of LIBS and SEM-EDX showed that Ca increases, and other elements decrease from surface to the sound inner parts of the stone due to calcium oxalate and gypsum precipitation and clay deposition on the surfaces. The calcium oxalate patina forms a homogeneous film layer on calcite crystals. It is most likely formed by the reaction of calcite and oxalic acid produced by the biological formations on stone surfaces. It is colorless in original. The yellow color may be related with the FeO and clay deposition on the stone surfaces. The outcomes of the study proved the presence of a protective yellow patina formation on yellow travertine surfaces against the weathering effects of water which cannot be distinguished by naked eye. This patina presents same characteristics with the yellow patina on marble surfaces which should be conserved. The results of this study show that the determination of yellow patina is critical to keep irreversible cleaning interventions away from surfaces especially for the monuments that yellow travertine is used as building materials.