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Wyszukujesz frazę "Solid phase extraction" wg kryterium: Temat


Tytuł:
Nanoadsorbents for the preconcentration of some toxic substances : a minireview
Autorzy:
Kaur, A.
Saini, S. S.
Powiązania:
https://bibliotekanauki.pl/articles/411821.pdf
Data publikacji:
2014
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
Solid phase extraction
preconcentration
trace analytes
Opis:
The development of new sorbents and their application in preconcentration methods for determination of trace analytes is subject of great interest. Sample pretreatment methods, such as separation / preconcentration prior to the determination of metal ions have developed rapidly due to the increasing need for accurate and precise measurements at extremely low levels of ions in diverse matrices. This review summarizes and discusses several analytical methods involving the preparation and use of new solid phase extractant. A literature survey of the last ten years offering a critical review of these new sorbents available for use in trace analyte enrichment is provided.
Źródło:
International Letters of Chemistry, Physics and Astronomy; 2014, 2; 22-35
2299-3843
Pojawia się w:
International Letters of Chemistry, Physics and Astronomy
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Rapid, sensitive and accurate method for determination of Lafutidine hydrochloride in human plasma by RP-HPLC system
Autorzy:
Vekariya, P. P.
Joshi, H. S.
Powiązania:
https://bibliotekanauki.pl/articles/412425.pdf
Data publikacji:
2014
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
HPLC-PDA
Human plasma
Solid phase Extraction
Opis:
Simple and rapid reverse phase high-performance liquid chromatography (RP-HPLC) method was developed and validated using Phenomenex Gemini c18 (4.6 x 250 mm, 5 μ) reverse phase column for the determination of LAF in human plasma, Solid Phase Extraction (SPE) technique was used for the extraction of analyte, detection was carried out by Photo Diode Array detector at 216 nm. Chromatographic resolution of the LAF was achieved within 4.6 min by using mobile phase Methanol and 5 mM Di-Potassium Hydrogen Phosphate Buffer (pH 9.5) (80:20, v/v), flow rate was 1.0 mL/min. Calibration curve was linear with correlation coefficient of 0.9996 in the range of 50-1000 ng/mL, Limit of Detection (LOD) and Limit of Quantitation (LOQ) were 10 ng/mL and 30 ng/mL respectively, intra and inter-day deviations were lower than 3.92 % and 3.98 % respectively. The overall mean recovery of LAF was 94.57 %. No any endogenous constituents were found to interfere at retention time of the analyte. This new RP-HPLC method was successfully validated and may be applied to conduct bioavailability & bioequivalence studies of LAF.
Źródło:
International Letters of Chemistry, Physics and Astronomy; 2014, 7; 9-20
2299-3843
Pojawia się w:
International Letters of Chemistry, Physics and Astronomy
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Determination of trace quantities of dutasteride in water and wastewater by solid phase extraction and high-performance liquid chromatography
Autorzy:
Wasilewska, A.
Madajczyk, M.
Szymański, A.
Urbaniak, W.
Powiązania:
https://bibliotekanauki.pl/articles/347041.pdf
Data publikacji:
2011
Wydawca:
Politechnika Bydgoska im. Jana i Jędrzeja Śniadeckich. Wydział Technologii i Inżynierii Chemicznej
Tematy:
dutasteride
emerging pollutants
solid-phase extraction (SPE)
liquid chromatography
HPLC
Opis:
Steroid compounds are a kind of pollutants which are increasingly more frequently found in environmental samples. Due to the ever more increasing level of such pollutants and their biological activity, they are of interest to analysts. Our study involved the development of a simple and fast method for the assay of dutasteride in treated industrial waste water using high-performance liquid chromatography. As the steroid concentration in water is much lower than the limit of detection of the UV detector used, the compound assayed in the test water was pre-concentrated using solid-phase extraction. Our procedure has high accuracy and a precision of 2.6%, and the recovery of the analyte from water is 78.6%. The procedure enables the assay of dutasteride at a level of 2 microg/L in water.
Źródło:
Ars Separatoria Acta; 2011, 8; 39-49
1731-6340
Pojawia się w:
Ars Separatoria Acta
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Adsorption efficiency of pentafluorobenzene on ionic liquids-based silicas
Autorzy:
Wang, X.
Lin, L.
Xie, J.
Yan, X.
Xiao, W.
Tian, P.
Powiązania:
https://bibliotekanauki.pl/articles/778559.pdf
Data publikacji:
2018
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
ionic liquids based silica
pentafl uorobenzene
adsorption
solid-phase extraction
Opis:
The adsorption of pentafl uorobenzene on nine ionic liquid-based silicas was investigated using solid phase extraction. The effects of several variables such as the type of ionic liquid groups, adsorption time, temperatures and water ratio in the solution system were experimentally evaluated. The imidazole-chloride ionic liquid group based silica exhibited the highest adsorption efficiency under the optimized conditions of 5 min adsorption at 30°C in water/methanol (30:70, vol%) solution. In addition, the effects of pH, as well as type and concentrations of chloride salts were investigated. At pH values other than neutral and high salt concentration, the adsorption efficiency was reduced. Finally, the relative standard deviation of less than 5.8% over a 5-day period showed a high precision for the nine tested sorbents.
Źródło:
Polish Journal of Chemical Technology; 2018, 20, 3; 47-52
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Chemical modification of silica surface by bonding ketoimine groups for SPE
Autorzy:
Rykowska, I.
Wasik, W.
Powiązania:
https://bibliotekanauki.pl/articles/346937.pdf
Data publikacji:
2008
Wydawca:
Politechnika Bydgoska im. Jana i Jędrzeja Śniadeckich. Wydział Technologii i Inżynierii Chemicznej
Tematy:
chemically bonded phases
silica gel
solid-phase extraction (SPE)
gas chromatography
Opis:
The applicability of silica gels, modified with ketoimine groups, in solid-phase extraction was tested. The surface characteristics of the modified silica was determined by elemental analysis, NMR spectra for the solid phases (29Si CP MAS NMR), analysis of pore size distribution of the silica support, and nitrogen adsorptiondesorption. The newly proposed sorbents with ketoimine groups were used for extraction of endocrine-disruptor compounds, extracted from water and powder milk. The properties of the sorbents were compared with commercial C18 ones.
Źródło:
Ars Separatoria Acta; 2008, 6; 41-52
1731-6340
Pojawia się w:
Ars Separatoria Acta
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Sample Preparation Followed by High Performance Liquid Chromatographic (HPLC) Analysis for Monitoring Muconic Acid as a Biomarker of Occupational Exposure to Benzene
Autorzy:
Shahtaheri, S. J.
Ghamari, F.
Golbabaei, F.
Rahimi-Froushani, A.
Abdollahi, M.
Powiązania:
https://bibliotekanauki.pl/articles/91059.pdf
Data publikacji:
2005
Wydawca:
Centralny Instytut Ochrony Pracy
Tematy:
benzene
muconic acid
sample preparation
solid-phase extraction
biological monitoring
chromatography
Opis:
Factors affecting solid phase extraction (SPE) of trans,trans-muconic acid (ttMA), as a benzene biomarker, including sample pH, sample concentration, sample volume, sample flow rate, washing solvent, elution solvent, and type of sorbent were evaluated. Extracted samples were determined by HPLC-UV (high performance liquid chromatography-ultraviolet). The analytical column was C18, UV wave length was 259 nm, and the mobile phase was H2O/methanol/acetic acid run at flow rate of 1 ml/min. A strong anion exchange silica cartridge was found successful in simplifying SPE. There was a significant difference between recoveries of ttMA when different factors were used (p < .001). An optimum recovery was obtained when sample pH was adjusted at 7. There was no significant difference when different sample concentrations were used (p > .05). The optimized method was then validated with 3 different pools of samples showing good reproducibility over 6 consecutive days and 6 within-day experiments.
Źródło:
International Journal of Occupational Safety and Ergonomics; 2005, 11, 4; 377-388
1080-3548
Pojawia się w:
International Journal of Occupational Safety and Ergonomics
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Determination of di-n-butyl Phthalate in Environmental Samples
Autorzy:
Ziembowicz, Sabina
Kida, Małgorzata
Powiązania:
https://bibliotekanauki.pl/articles/27315758.pdf
Data publikacji:
2023
Wydawca:
Politechnika Koszalińska. Wydawnictwo Uczelniane
Tematy:
di-n-butyl phthalate
aqueous samples
landfill leachate
solid phase extraction
method validation
Opis:
A devised methodology presented here allows the determination of di-n-butyl phthalate in environmental samples (water and landfill leachate) using solid-phase extraction (SPE) and gas chromatography. It is developed based on the use of a gas chromatograph with an FID detector. Preliminary testing has also provided extraction parameters and conditions for chromatographic determination, with calibration applied by reference to an internal standard. The linearity of the calibration curve has been tested in DBP concentrations ranging from 0 to 7.5 mg/L, with the data obtained showing that, throughout this range, the detector readings as a function of the DBP concentrations remain linear (R2 coefficient >0.99). The average levels of recovery of DBP from aqueous solutions of phthalates are in the range of 97-109%, while the corresponding figures for leachates are 85-101%. The values of the coefficients of variation associated with the results obtained do not exceed 5%. The results, therefore, indicate that the applied extraction method is effective as regards DBP extraction from both water and landfill leachate, while numerous other substances present in the leachate from landfill sites apparently do not affect the correct determination of di-n-butyl phthalate by the method developed.
Źródło:
Rocznik Ochrona Środowiska; 2023, 25; 242--249
1506-218X
Pojawia się w:
Rocznik Ochrona Środowiska
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
UV-Vis spectroscopic detection coupled with chemometrics for the measurement of mixed organic acids in water samples enriched by radial electric focusing solid phase extraction
Autorzy:
Guo, Y.
Liu, X.
Liu, J.
Bian, X.
Zhang, Q.
Pan, J.
Wan, D.
Powiązania:
https://bibliotekanauki.pl/articles/221808.pdf
Data publikacji:
2018
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
chemometrics
UV-Vis spectrophotometer
radial electric focusing solid phase extraction
mixed organic acids
Opis:
Due to the difficulty of detecting traces of organic acid mixture in an aqueous sample and the complexity of resolving UV-Vis spectra effectively, a combinatory method based on a self-made radical electric focusing solid phase extraction (REFSPE) device, UV-Vis detection and partial least squares (PLS) calculation is proposed here. In this study, REFSPE was used to enhance the extraction process of analytes between the aqueous phase and the membrane phase to enrich the trace of mixed organic acid efficiently. Then, the analytes, which were eluted from the adsorption film by ethanol with the assistance of an ultrasonic cleaning machine, were detected with UV-Vis spectrophotometry. After that, the PLS method was introduced to solve the problem of overlapping peaks in UV-Vis spectra of mixed substances and to quantify each compound. The linearly dependent coefficients between the predicted value of the model and the actual concentration of the sample were all higher than 0.99. The limit values of detection for benzoic acid, phthalic acid and p-toluene sulfonic acid were found at 9.9 μg/L, 12.2 μg/L and 13.8 μg/L with the relative recovery values between 84.8% and 117.9%. The RSD (n = 20) values of each component are 1.17%, 1.11% and 0.86%, respectively. Therefore, the proposed combined method can determine traces of complex materials in an aqueous sample efficiently and has wonderful potential applications.
Źródło:
Metrology and Measurement Systems; 2018, 25, 2; 317-329
0860-8229
Pojawia się w:
Metrology and Measurement Systems
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Ascertaining optimal protocols for DNA extraction of different qualities of pike (Esox lucius) tissue samples - a comparison of commonly used solid phase extraction methods
Autorzy:
Eschbach, E.
Powiązania:
https://bibliotekanauki.pl/articles/363074.pdf
Data publikacji:
2012
Wydawca:
Uniwersytet Warmińsko-Mazurski w Olsztynie
Tematy:
szczupak
Esox lucius
ekstrakcja DNA
ekstrakcja do fazy stałej
pike
DNA extractions
solid-phase extraction
Opis:
High quality DNA extractions are a prerequisite for genetic studies of a variety of organisms including fish. The current study focused on the applicability of different commercially available solid phase extraction (SPE) methods as the easiest and fastest methods for DNA extraction and their efficiency with different tissue qualities. These were represented by different kinds of pike tissues (fins, muscle, scales) preserved with different methods and stored at different temperatures over different periods of time (0.5 to 10.0 years). All DNA extractions were analysed according to their yield, purity, integrity and functionality in PCR based downstream analysis. Additionally mechanical pre-treatment of poor quality tissues (e.g. old or aged tissues) and efficient ethanol preservation of frozen bulk fin tissue were investigated. All SPE methods yielded functional DNA from very different qualities of pike tissues as shown by PCR analysis of small nuclear (microsatellite) and large mitochondrial (complete D-loop) DNA fragments. DNA from poor quality tissue can be extracted using single column SPE and in some cases mechanical pre-treatment even improved the yield. Good quality tissue as obtained e.g. from commercial fishermen as frozen bulk material is more efficiently preserved by thawing in ethanol at room temperature than at 2-8°C. DNA from these and air dried tissues was very efficiently prepared by applying reverse SPE in 96-well format, allowing for fast processing of a multitude of samples for high throughput analysis.
Źródło:
Environmental Biotechnology; 2012, 8, 1; 7-14
1734-4964
Pojawia się w:
Environmental Biotechnology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Zastosowanie ekstrakcji do fazy stałej w analizie lotnych związków zapachowych ogórka
Application of the solid phase extraction for the evaluating the volatile aroma compounds of cucumber
Autorzy:
Gośliński, M.
Dziadas, M.
Zawirska-Wojtasiak, R.
Powiązania:
https://bibliotekanauki.pl/articles/270508.pdf
Data publikacji:
2011
Wydawca:
Centralny Ośrodek Badawczo-Rozwojowy Aparatury Badawczej i Dydaktycznej, COBRABiD
Tematy:
lotne związki aromatyczne
ekstrakcja do fazy stałej (SPE)
volatile aroma compounds
solid-phase extraction (SPE)
Opis:
Ekstrakcja do fazy stałej SPE jest techniką stosowaną powszechnie do selektywnej izolacji analitów z ciekłych matryc. Może być wykorzystana do przygotowania prób analizowanych metodami chromatografii gazowej. W niniejszej pracy przedstawiono zastosowanie techniki SPE w analizie lotnych związków zapachowych ogórka. Zidentyfikowano główne związki lotne, a następnie porównano ich zawartość pomiędzy poszczególnymi próbami owoców ogórka transgenicznego. Otrzymane wyniki były porównywalne z wcześniejszymi wynikami badań własnych uzyskanymi za pomocą innych technik analitycznych. Ekstrakcja SPE może stanowić alternatywę lub uzupełnienie dla dotychczasowych oznaczeń substancji zapachowych.
Solid phase extraction (SPE) is a common technique applied to selective isolation of compounds from liquid matrix. It can be use in sample preparation for gas chromatography. The aim of this study was the application of SPE technique for evaluating the aroma of cucumber. The main volatiles were determined and then the comparison of their concentration between different cucumber samples was done. The results were comparable with those obtained previously by other analytical methods. The SPE technique could be an alternative or complement tool in the analysis of volatiles.
Źródło:
Aparatura Badawcza i Dydaktyczna; 2011, 16, 1; 79-82
2392-1765
Pojawia się w:
Aparatura Badawcza i Dydaktyczna
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Determination of acidic pharmaceuticals in municipal wastewater by using solid-phase extraction followed by gas chromatography-mass spectrometry
Oznaczanie kwasowych leków w ściekach komunalnych metodą chromatografii gazowej ze spektrometrem mas z wykorzystaniem ekstrakcji do fazy stałej
Autorzy:
Nosek, K.
Styszko, K.
Gołaś, J.
Powiązania:
https://bibliotekanauki.pl/articles/1510655.pdf
Data publikacji:
2012
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Wydawnictwo AGH
Tematy:
pharmaceuticals
wastewater
GC-MS
solid-phase extraction
derivatization
farmaceutyki
ścieki komunalne
ekstrakcja do fazy stałej
derywatyzacja
Opis:
Obecność farmaceutyków i ich metabolitów w środowisku wodnym stanowi stosunkowo nowy problem w dziedzinie chemii analitycznej i środowiskowej, ale skupiający coraz większe grono zainteresowanych ze względu na bioaktywny charakter tych zanieczyszczeń. W artykule przedstawiono procedurę oznaczania wybranych substancji leczniczych z grupy niesteroidowych leków przeciwzapalnych, takich jak ketoprofen, naproksen i diklofenak oraz innych nowo pojawiających się zanieczyszczeń - triclosanu i bisfenolu A w oczyszczonych i surowych ściekach komunalnych. Próbki ścieków zatężono i oczyszczono metodą ekstrakcji do fazy stałej (SPE). Składniki ekstraktu przeprowadzono w pochodne lotne w reakcji silylacji z N-metylo-N-trimetylsililo trifluoroacetamidem (MSTFA), a analizę próbek ścieków wykonano w technice chromatografii gazowej ze spektrometrem mas. Wszystkie z badanych farmaceutyków zostały oznaczone zarówno w ściekach oczyszczonych, jak i surowych w stężeniach rzędu od ppt to ppb.
The appearance of pharmaceutical compounds and the need of their determination in an aquatic environment has become a subject of growing concern over recent years. This paper describes an application of a quantitative analytical method for the determination of selected nonsteroidal anti-inflammatory drugs: ketoprofen, naproxen, diclofenac and other newly emerging contaminants - triclosan and bisphenol A in influent and effluent from a wastewater treatment plant located in Kraków (Poland). Samples were isolated and preconcentrated by using the solid - phase extraction (SPE) technique, then eluat was derivatized with N-methy-N-(trimethylsilyl)-trifluoroacetamide (MSTFA) and analyzed by gas chromatography coupled with mass spectrometry. All of tested pharmaceuticals were present in the wastewater treatment plant effluent and influent at concentration ppt to ppb.
Źródło:
Geomatics and Environmental Engineering; 2012, 6, 3; 45-60
1898-1135
Pojawia się w:
Geomatics and Environmental Engineering
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Optimisation and validation of the analytical procedure for the determination of acrylamide in coffee by LC-MS/MS with SPE clean up
Autorzy:
Gielecinska, I.
Mojska, H.
Powiązania:
https://bibliotekanauki.pl/articles/875236.pdf
Data publikacji:
2013
Wydawca:
Narodowy Instytut Zdrowia Publicznego. Państwowy Zakład Higieny
Tematy:
optimization
validation
analytical procedure
determination
acrylamide
coffee
liquid chromatography
tandem mass spectrometry method
solid-phase extraction
Opis:
Background. Numerous studies have demonstrated acrylamide to be both neurotoxic and carcinogenic. At present it is widely recognised that acrylamide is mainly formed through the Maillard reaction from free asparagine and reducing sugars. The major sources of dietary acrylamide are potato products, processed cereals and coffee. Objective. To optimise and validate an analytical method for determining acrylamide in coffee by liquid chromatography and tandem mass spectrometry analysis (LC/MS/MS) using SPE clean-up. Material and methods. Analytical separation of acrylamide from roasted coffee was performed by liquid chromatography using a Hypercarb column followed by LC/MS/MS analysis, with 2,3,3–d3 acrylamide as an internal standard. The method was based on two purification steps: the first with hexane and Carrez solutions in order to remove of fat and to precipitate proteins, respectively; and the second with a solid-phase extraction (SPE) column which proved to be efficient in the elimination of the main chromatographic interferences. Results. Limit of quantification (LOQ) for measuring acrylamide in coffee was 50 μg/kg. The described method demonstrates satisfactory precision (RSD = 2.5%), repeatability (RSD = 9.2%) and accuracy (mean recovery – 97.4%). Conclusions. Our results confirm that LC-MS/MS with SPE clean-up is selective and suitable for determination of acrylamide in coffee. Indeed, this method meets the criteria of EU Commission Recommendations (No. 2007/331/EC and No. 2010/307/EU), on the monitoring of acrylamide levels in food.
Wprowadzenie. W licznych badaniach wykazano, że akryloamid jest związkiem neurotoksycznym i kancerogennym. Obecnie wiadomo, że akryloamid w żywności powstaje w wyniku reakcji Maillarda pomiędzy wolną asparaginą a cukrami redukującymi. Głównym źródłem akryloamidu w diecie człowieka są produkty ziemniaczane, przetwory zbożowe oraz kawa. Cel. Optymalizacja warunków procedury analitycznej i walidacja metody oznaczania zawartości akryloamidu w różnych rodzajach kawy techniką wysokosprawnej chromatografii cieczowej sprzężonej z tandemową spektrometrią mas (LC-MS/ MS) z wykorzystaniem ekstrakcji do fazy stałej (SPE). Materiał i metody. Akryloamid w kawie palonej oznaczono na kolumnie Hypercarb metodą chromatografii cieczowej sprzężonej z tandemową spektrometrią mas (LC-MS/MS). Jako wzorzec wewnętrzny zastosowano 2,3,3-d3 akryloamid. W metodzie tej zastosowano 2 stopniowy proces oczyszczania próbki: w pierwszej kolejności usunięto tłuszcz heksanem oraz strącono białka poprzez dodanie roztworów Carreza, a następnie wykorzystując ekstrakcję do fazy stałej (SPE) próbkę oczyszczono z pozostałych zanieczyszczeń, które mogłyby mieć wpływ na wynik w czasie analizy chromatograficznej. Wyniki. Granica oznaczalności metody LC-MS/MS oznaczania akryloamidu w kawie wynosi 50 μg/kg. Opracowana metoda charakteryzuje się dobrą precyzją (RSD = 2,5%), powtarzalnością (RSD = 9,2%) oraz dokładnością (średni odzysk = 97,4%). Wnioski. Wyniki walidacji potwierdzają selektywność i przydatność opracowanej metody do oznaczania akryloamidu w kawie. Opracowana metoda LC-MS/MS spełnia wymagania zaleceń Komisji Unii Europejskiej (2007/331/EC i 2010/307/ EU) w sprawie monitorowania poziomów akryloamidu w żywności.
Źródło:
Roczniki Państwowego Zakładu Higieny; 2013, 64, 2
0035-7715
Pojawia się w:
Roczniki Państwowego Zakładu Higieny
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Volatile profiles of toxigenic and non-toxigenic Aspergillus flavus using SPME for solid phase extraction
Autorzy:
De, Lucca A J
Boue, S.M.
Carter-Wientjes, C.H.
Bland, J.M.
Bhatnagar, D.
Cleveland, T.E.
Powiązania:
https://bibliotekanauki.pl/articles/50286.pdf
Data publikacji:
2010
Wydawca:
Instytut Medycyny Wsi
Tematy:
Aspergillus flavus
toxigenic strain
non-toxigenic strain
secondary metabolite
aflatoxin
maize
volatile profile
solid-phase microextraction
solid-phase extraction
potato
isolate
Źródło:
Annals of Agricultural and Environmental Medicine; 2010, 17, 2; 301-308
1232-1966
Pojawia się w:
Annals of Agricultural and Environmental Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Nanomateriały opracowane na potrzeby dyspersyjnej ekstrakcji do fazy stałej, część 1 – modyfikacje materiałów klasycznych
Nanomaterials developed for dispersive solid phase extraction, part 1 – modifications of classical materials
Autorzy:
Ścigalski, Piotr
Kosobucki, Przemysław
Powiązania:
https://bibliotekanauki.pl/articles/2057914.pdf
Data publikacji:
2022
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
chemia analityczna
dyspersyjna ekstrakcja do fazy stałej
nowe sorbenty
nanomateriały
analytical chemistry
dispersive solid phase extraction
novel sorbents
nanomaterials
Opis:
Solid phase extraction (SPE) is an analytical procedure developed with the purpose of separating a target analyte from a complex sample matrix prior to quantitative or qualitative determination. The purpose of such treatment is twofold: elimination of matrix constituents that could interfere with the detection process or even damage analytical equipment as well as enriching the analyte in the sample so that it is readily available for detection. Dispersive solid phase extraction (dSPE) is a relatively recent development of the standard SPE technique that is attracting growing attention due to its remarkable simplicity, short extraction time and low requirement for solvent expenditure, accompanied by high effectiveness and wide applicability. There is an enormous abundance of articles concerning advances in sample preparation and analysis published every year. The aim of this review is to bring to closer attention developments of materials with potential application as sorbents in dSPE technique through a thorough survey of recently conducted analytical studies focusing on methods utilizing novel, interesting nanomaterials in dSPE procedures and evaluation of their performance and suitability based on comparison of provided validation parameters with previously reported analytical procedures. The first part of this review focuses on widely known and utilized materials such as silica and carbon and their modifications, up to and including graphene and carbon nanotubes. Studies chosen for this review will be listed in tables alongside their relevant validation parameters at the end of each chapter. Applications found to be particularly interesting due to high effectiveness, unusual operating procedure or scope, among other reasons, will be described in greater detail.
Źródło:
Wiadomości Chemiczne; 2022, 76, 1-2; 27-42
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Nanomateriały opracowane na potrzeby dyspresyjnej ekstrakcji do fazy stałej. Cz. 2, Materiały współczesne
Recent nanomaterials developed for dispresive solid phase extraction. Part 2, Modern materials
Autorzy:
Ścigalski, Piotr
Kosobucki, Przemysław
Powiązania:
https://bibliotekanauki.pl/articles/2200598.pdf
Data publikacji:
2022
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
chemia analityczna
dyspersyjna ekstrakcja do fazy stałej
nowe sorbenty
nanomateriały
analytical chemistry
dispersive solid phase extraction
novel sorbents
nanomaterials
Opis:
The second part of the review shifts attention to novel modern materials applied to dSPE as sorbents, that are often designed specifically for the extraction of a particular analyte. This part will focus on advances in materials such a molecularly imprinted polymers (MIP), metallic organic frameworks (MOF), layered double hydroxides (LDH) or magnetic nanoparticles (MNP). As in the first part, studies chosen for this review will be listed in tables alongside their relevant validation parameters at the end of each chapter. Studiesfound to be particularly interesting due to high effectiveness, unusual operating procedure or scope, among other reasons, will be described in greater detail.
Źródło:
Wiadomości Chemiczne; 2022, 76, 1-2; 43-57
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł

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