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Journal articles on the topic 'Solid-phase extraction'

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Published: 4 June 2021
Last updated: 1 June 2024

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1

Tippins, B. "Solid phase extraction fundamentals." Nature 334, no. 6179 (July 1988): 273–74. http://dx.doi.org/10.1038/334273a0.

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2

Pawliszyn, J. "Analytical Solid-Phase Extraction." Analytica Chimica Acta 419, no. 1 (August 2000): 115. http://dx.doi.org/10.1016/s0003-2670(00)00914-4.

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3

Šafařı́ková, Mirka, and Ivo Šafařı́k. "Magnetic solid-phase extraction." Journal of Magnetism and Magnetic Materials 194, no. 1-3 (April 1999): 108–12. http://dx.doi.org/10.1016/s0304-8853(98)00566-6.

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4

Butcher, David J. "Analytical solid-phase extraction." Microchemical Journal 65, no. 1 (July 2000): 99. http://dx.doi.org/10.1016/s0026-265x(00)00020-5.

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5

Maharramova, L. M., N. E. Jabbarova, and M. Y. Abdullayeva. "EXTRACTION OF NICKEL (II) PICRATE FROM SOLID PHASE WITH ORGANIC REAGENTS." Chemical Problems 21, no. 3 (2023): 221–28. http://dx.doi.org/10.32737/2221-8688-2023-3-221-228.

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The present work is dedicated to the very important area of analytical chemistry—extractionphotometric determination of ions from a solid phase. We carried out studies on the extraction of nickel picrate (NiPik2) from the solid phase using solutions of tetrahalobicyclic reagents of the acetylene series with a dicarbonyl bridge in the side chain (L1, L2, L3, L4) of chloroform. New organic ligands were synthesized and their physicochemical properties - melting point, molecular weights, as well as their optical density studied. A new technique for the extraction-photometric determination of the nickel ion from the solid phase was developed. It found that new organic reagents (L1-L4) exhibit high extraction ability (0.11-0.64 mg/l) of Ni ions from the solid phase. When comparing the extraction activity of the studied reagents, it was revealed that the ability to extract organic ligands of tetrahalobicyclic reagents (L1-L4) changes in the following order: L4> L3> L1> L2. Magnetic field increased nickel extraction by 3-4%.
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6

Kanafusa, Sumiyo. "Solid Phase Micro Extraction: SPME." Nippon Shokuhin Kagaku Kogaku Kaishi 65, no. 4 (2018): 215. http://dx.doi.org/10.3136/nskkk.65.215.

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7

Płotka-Wasylka, Justyna, Natalia Szczepańska, Miguel de la Guardia, and Jacek Namieśnik. "Miniaturized solid-phase extraction techniques." TrAC Trends in Analytical Chemistry 73 (November 2015): 19–38. http://dx.doi.org/10.1016/j.trac.2015.04.026.

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8

Rodrı́guez, I., M. P. Llompart, and R. Cela. "Solid-phase extraction of phenols." Journal of Chromatography A 885, no. 1-2 (July 2000): 291–304. http://dx.doi.org/10.1016/s0021-9673(00)00116-3.

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9

Tang, De-Song, Hui-Ling Liang, Lin Zhang, and Huan-Lin Chen. "Solid Phase Extraction of Solanesol." Chromatographia 66, no. 1-2 (June 6, 2007): 129–31. http://dx.doi.org/10.1365/s10337-007-0251-5.

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10

Chisvert, Alberto, Soledad Cárdenas, and Rafael Lucena. "Dispersive micro-solid phase extraction." TrAC Trends in Analytical Chemistry 112 (March 2019): 226–33. http://dx.doi.org/10.1016/j.trac.2018.12.005.

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11

Stevenson, D. "Immuno-affinity solid-phase extraction." Journal of Chromatography B: Biomedical Sciences and Applications 745, no. 1 (August 2000): 39–48. http://dx.doi.org/10.1016/s0378-4347(00)00204-8.

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12

Carson, Mary C. "Ion-pair solid-phase extraction." Journal of Chromatography A 885, no. 1-2 (July 2000): 343–50. http://dx.doi.org/10.1016/s0021-9673(00)00471-4.

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13

Molins-Legua, C., and P. Campins-Falcó. "Solid phase extraction of amines." Analytica Chimica Acta 546, no. 2 (August 2005): 206–20. http://dx.doi.org/10.1016/j.aca.2005.05.021.

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14

Shen, Yao, Yumin Hu, Ke Huang, Shi’an Yin, Bo Chen, and Shouzhuo Yao. "Solid-phase extraction of carotenoids." Journal of Chromatography A 1216, no. 30 (July 2009): 5763–68. http://dx.doi.org/10.1016/j.chroma.2009.06.009.

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15

Ravelo-Pérez, Lidia M., Antonio V. Herrera-Herrera, Javier Hernández-Borges, and Miguel Ángel Rodríguez-Delgado. "Carbon nanotubes: Solid-phase extraction." Journal of Chromatography A 1217, no. 16 (April 2010): 2618–41. http://dx.doi.org/10.1016/j.chroma.2009.10.083.

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16

Gao, Kun Yang, Xiao Feng Huang, Yong Yang, Lei Yang, Qi Dong Xia, Yan Fu Wei, Tao Zhou, and Yang Song Qin. "Advances on the Extraction and Separation Technologies in Tea Aroma Components Research." Advanced Materials Research 301-303 (July 2011): 421–25. http://dx.doi.org/10.4028/www.scientific.net/amr.301-303.421.

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Study on the tea aroma components is greatly significant, which are important factors in tea quality valuation.In recent years, nine main methods are under consideration：simultaneous distillation and solvent extraction, vacuum distillation extraction, steam distillation under reduced pressure, headspace analysis, solid-phase micro-extractions, headspace solid-phase micro-extractions, tea liquid absorption, supercritical fluid extraction and electronic nose. Meanwhile, advantages and disadvantages of each method were analyzed, in order to conduct technological guidance on the extraction and separation technologies in tea aroma components and provide a theoretical basis in improvement of each method.
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17

Shyam Sunder, Govind Sharma, Sandhya Adhikari, Ahmad Rohanifar, Abiral Poudel, and Jon R. Kirchhoff. "Evolution of Environmentally Friendly Strategies for Metal Extraction." Separations 7, no. 1 (January 6, 2020): 4. http://dx.doi.org/10.3390/separations7010004.

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The demand for the recovery of valuable metals and the need to understand the impact of heavy metals in the environment on human and aquatic life has led to the development of new methods for the extraction, recovery, and analysis of metal ions. With special emphasis on environmentally friendly approaches, efforts have been made to consider strategies that minimize the use of organic solvents, apply micromethodology, limit waste, reduce costs, are safe, and utilize benign or reusable materials. This review discusses recent developments in liquid- and solid-phase extraction techniques. Liquid-based methods include advances in the application of aqueous two- and three-phase systems, liquid membranes, and cloud point extraction. Recent progress in exploiting new sorbent materials for solid-phase extraction (SPE), solid-phase microextraction (SPME), and bulk extractions will also be discussed.
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18

KATSUMATA, Hideyuki. "Solid-Phase Extraction for Environmental Analysis." Analytical Sciences 35, no. 12 (December 10, 2019): 1289–90. http://dx.doi.org/10.2116/analsci.highlights1912.

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19

Johannes, I., L. Mölder, and L. Tiikma. "EVALUATION OF SOLID PHASE EXTRACTION LIMITS." Oil Shale 14, no. 1 (1997): 41. http://dx.doi.org/10.3176/oil.1997.1.03.

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20

Walker, Valerie, and Graham A. Mills. "Solid-phase extraction in clinical biochemistry." Annals of Clinical Biochemistry: International Journal of Laboratory Medicine 39, no. 5 (September 1, 2002): 464–77. http://dx.doi.org/10.1258/000456302320314476.

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In order to measure low concentrations of analytes in plasma and urine, it is often necessary to extract and concentrate them. With solid-phase extraction (SPE), this is achieved by partitioning the analytes between a solid and a liquid or headspace vapour. A wide range of high-quality materials is now available to do this, offering a variety of separation modes for different applications. These include partitioning using reversed-phase, normal-phase, ion-exchange, restricted-access and immunoaffinity sorbents or molecularly imprinted polymers and, increasingly, combinations of these processes. Solid-phase microextraction was introduced to analyse volatile and semi-volatile compounds. The range of sampling formats has expanded from simple packed syringes to cartridges, disks, SPE pipette tips and 96-well plates. These developments have facilitated automated off- and on-line sample processing. The basic principles of SPE and the recent innovations are reviewed here. This is a technological growth area. Some of the developments are finding application in clinical toxicology. However, they could also be of wider value in clinical chemistry - for example, for analyses of volatile and non-volatile metabolites, peptides, radioactive elements and trace metal speciation.
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21

Jamali, Mohammad Reza, Ahmad Firouzjah, and Reyhaneh Rahnama. "Solvent-assisted dispersive solid phase extraction." Talanta 116 (November 2013): 454–59. http://dx.doi.org/10.1016/j.talanta.2013.07.023.

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22

Chigome, Samuel, and Nelson Torto. "Electrospun nanofiber-based solid-phase extraction." TrAC Trends in Analytical Chemistry 38 (September 2012): 21–31. http://dx.doi.org/10.1016/j.trac.2012.04.011.

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23

Fontanals, Núria, Francesc Borrull, and Rosa M. Marcé. "Ionic liquids in solid-phase extraction." TrAC Trends in Analytical Chemistry 41 (December 2012): 15–26. http://dx.doi.org/10.1016/j.trac.2012.08.010.

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24

Hennion, Marie-Claire. "Graphitized carbons for solid-phase extraction." Journal of Chromatography A 885, no. 1-2 (July 2000): 73–95. http://dx.doi.org/10.1016/s0021-9673(00)00085-6.

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25

Wells, Martha J. M., and Lan Zhou Yu. "Solid-phase extraction of acidic herbicides." Journal of Chromatography A 885, no. 1-2 (July 2000): 237–50. http://dx.doi.org/10.1016/s0021-9673(00)00206-5.

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26

Poole, Colin F. "New trends in solid-phase extraction." TrAC Trends in Analytical Chemistry 22, no. 6 (June 2003): 362–73. http://dx.doi.org/10.1016/s0165-9936(03)00605-8.

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27

Nilsson, Ulf J. "Solid-phase extraction for combinatorial libraries." Journal of Chromatography A 885, no. 1-2 (July 2000): 305–19. http://dx.doi.org/10.1016/s0021-9673(99)01095-x.

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28

Puziy, A. M., O. I. Poddubnaya, B. Gawdzik, M. Sobiesiak, C. A. Reinish, M. M. Tsyba, T. P. Segeda, and M. I. Danylenko. "Nanostructured carbons for solid phase extraction." Applied Surface Science 256, no. 17 (June 2010): 5216–20. http://dx.doi.org/10.1016/j.apsusc.2009.12.106.

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29

Rostagno, Mauricio A., Miguel Palma, and Carmelo G. Barroso. "Solid-phase extraction of soy isoflavones." Journal of Chromatography A 1076, no. 1-2 (May 2005): 110–17. http://dx.doi.org/10.1016/j.chroma.2005.04.045.

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30

Konstantakopoulos, I. C., and A. G. Andreopoulos. "Polymer Networks for Solid Phase Extraction." Journal of Macromolecular Science, Part A 34, no. 5 (May 1997): 907–13. http://dx.doi.org/10.1080/10601329708014340.

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31

Camel, Valérie. "Solid phase extraction of trace elements." Spectrochimica Acta Part B: Atomic Spectroscopy 58, no. 7 (July 2003): 1177–233. http://dx.doi.org/10.1016/s0584-8547(03)00072-7.

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32

Rendl, Martin, Thomas Brandstetter, and Jürgen Rühe. "Solid-Phase Extraction in Segmented Flow." Langmuir 30, no. 43 (October 23, 2014): 12804–11. http://dx.doi.org/10.1021/la502645z.

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33

Kutter, J�rg P., Stephen C. Jacobson, and J. Michael Ramsey. "Solid phase extraction on microfluidic devices." Journal of Microcolumn Separations 12, no. 2 (2000): 93–97. http://dx.doi.org/10.1002/(sici)1520-667x(2000)12:2<93::aid-mcs5>3.0.co;2-p.

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34

Suttnar, Jiřı́, Jaroslav Čermák, and Jan Evangelista Dyr. "Solid-Phase Extraction in Malondialdehyde Analysis." Analytical Biochemistry 249, no. 1 (June 1997): 20–23. http://dx.doi.org/10.1006/abio.1997.2157.

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35

Vieira, Eny M., and Francis I. Onuska. "Extraction and Determination of RDX and HMX in Water." Water Quality Research Journal 34, no. 3 (August 1, 1999): 533–44. http://dx.doi.org/10.2166/wqrj.1999.026.

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Abstract The analysis of energetic materials such as RDX and HMX in water at trace levels was accomplished by using micro-extraction by miscible solvents, such as acetonitrile, 2-propanol and acetone, and salting out the organic phase. This paper compares the results obtained with solid-phase extraction (SPE) to those obtained by demixing techniques for spiked Milli-Q water and an unfiltered lake water. A review of the data indicates that demixing with acetonitrile-sodium chloride and 2-propanol ammonium sulfate gives better extraction recoveries than solid-phase extraction. Salting-out extractions are performed in less time and with less solvent than by SPE techniques.
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36

Hosseini, Maryam, Hasan Abbasinia, Abdorrasoul Malekpour, Tahereh Tarian, Asiyeh Hashemi, Reza Khoshnoud, Saeid Gholamzadeh, and Mohammad Zarenezhad. "MODIFIED SOLID PHASE EXTRACTION OF ORGANOPHOSPHORUS PESTICIDES; REPORT OF TWO CASES OF SUICIDES." International Journal of Pharmacy and Biological Sciences 6, no. 3 (July 1, 2016): 74–77. http://dx.doi.org/10.21276/ijpbs.2016.6.3.8.

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37

Zhang, Peixu, Xuwen Li, Li Cui, Jiafeng Chen, Yan Qu, Xiaozhong Wang, Qian Wu, Ying Liu, Chunkui Zhou, and Yongri Jin. "A novel storage and extraction method using solid-phase adsorption and ultrasonic-assisted nebulization extraction coupled to solid phase extraction." Analytical Methods 9, no. 33 (2017): 4863–72. http://dx.doi.org/10.1039/c7ay01036b.

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38

Dopico-García, M. S., P. Valentão, A. Jagodziñska, J. Klepczyñska, L. Guerra, P. B. Andrade, and R. M. Seabra. "Solid-phase extraction versus matrix solid-phase dispersion: Application to white grapes." Talanta 74, no. 1 (November 15, 2007): 20–31. http://dx.doi.org/10.1016/j.talanta.2007.05.022.

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39

Obukohwo, Dr Aghogho Blessing. "Review on Processes in Liquid-Liquid and Solid Phase Extraction." International Journal for Research in Applied Science and Engineering Technology 11, no. 1 (January 31, 2023): 1276–86. http://dx.doi.org/10.22214/ijraset.2023.48272.

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Abstract: The process of separating a component of mixture of liquid using liquid solvent is known as solvent extraction. The component being separated is completely insoluble in the solvent known as the carrier liquid. Distribution coefficient and partition coefficient are used to quantitatively determine the degree of solubility of a solute in a solvent compared to its solubility in another solvent. In liquid-liquid extraction (LLE) the solvents used should have maximum transfer of solute from carrier into the solvent. The solvent used must have high affinity for the solute to be extracted and it must not be completely miscible with the carrier liquid. Solid phase extraction (SPE) is a solvent-extraction system with a stationary phase by adsorption onto a solid support (usually silica) and the other liquid phase which is mobile. It uses small membranes or columns and many of the extracting agents used in LLE are also used in SPE. SPE generates less amount of wastes and it is an excellent substitute for LLE as it is faster and more efficient. It requires samples as small as 50 – 500ul and relatively small volumes of solvents not as pure as may be required by LLE. The working principles of SPE are like that of LLE were partitioning takes place between two immiscible liquids but in SPE the analytes to be extracted are partitioned between liquid and solid. This paper has reviewed the various processes involved in solvent extraction considering diluents in solvent extraction, liquid-liquid extraction and solidphase extraction.
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40

Chen, Fajun, and Hongmei Ming. "Liquid-liquid Extraction and Solid Phase Extraction to Identify the Volatile Components of Luzhou-flavor Liquor." International Journal of Biology and Life Sciences 5, no. 2 (March 29, 2024): 64–71. http://dx.doi.org/10.54097/7h5cbd72.

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In this paper, trace volatile components in Luzhou flavor Baijiu were analyzed by using different solvents, liquid-liquid extraction and solid-phase extraction combined with gas chromatography-mass spectrometry. A total of 166 substances were identified, including 23 substances with concentrations above 10mg/L, 9 substances with concentrations between 5mg/L-10mg/L, 38 substances with concentrations between 1mg/L-5mg/L, and the remaining 96 substances with concentrations below 1mg/L. There is a certain degree of complementarity between compounds extracted by solvents with different polarities, and solid-phase extraction performs poorly in extracting compounds with higher polarities.
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41

Jayasinghe, G. D. Thilini Madurangika, and Antonio Moreda-Piñeiro. "Molecularly Imprinted Polymers for Dispersive (Micro)Solid Phase Extraction: A Review." Separations 8, no. 7 (July 6, 2021): 99. http://dx.doi.org/10.3390/separations8070099.

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The review describes the development of batch solid phase extraction procedures based on dispersive (micro)solid phase extraction with molecularly imprinted polymers (MIPs) and magnetic MIPs (MMIPs). Advantages and disadvantages of the various MIPs for dispersive solid phase extraction and dispersive (micro)solid phase extraction are discussed. In addition, an effort has also been made to condense the information regarding MMIPs since there are a great variety of supports (magnetite and magnetite composites with carbon nanotubes, graphene oxide, or organic metal framework) and magnetite surface functionalization mechanisms for enhancing MIP synthesis, including reversible addition-fragmentation chain-transfer (RAFT) polymerization. Finally, drawbacks and future prospects for improving molecularly imprinted (micro)solid phase extraction (MIMSPE) are also appraised.
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42

Kraševec, Ida, and Helena Prosen. "Solid-Phase Extraction of Polar Benzotriazoles as Environmental Pollutants: A Review." Molecules 23, no. 10 (September 29, 2018): 2501. http://dx.doi.org/10.3390/molecules23102501.

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Polar benzotriazoles are corrosion inhibitors with widespread use; they are environmentally characterized as emerging pollutants in the water system, where they are present in low concentrations. Various extraction methods have been used for their separation from various matrices, ranging from classical liquid–liquid extractions to various microextraction techniques, but the most frequently applied extraction technique remains the solid-phase extraction (SPE), which is the focus of this review. We present an overview of the methods, developed in the last decade, applied for the determination of benzotriazoles in aqueous and solid environmental samples. Several other matrices, such as human urine and plant material, are also considered in the text. The methods are reviewed according to the determined compounds, sample matrices, cartridges and eluents used, extraction recoveries and the achieved limits of quantification. A critical evaluation of the advantages and drawbacks of the published methods is given.
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43

SATOH, Motoaki. "Solid Phase Extraction in Pesticides Residue Analysis." Journal of Pesticide Science 27, no. 4 (2002): 444–46. http://dx.doi.org/10.1584/jpestics.27.444.

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44

Junk, G. A., and J. J. Richard. "Solid-phase extraction on a small-scale." Journal of Research of the National Bureau of Standards 93, no. 3 (May 1988): 274. http://dx.doi.org/10.6028/jres.093.042.

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45

Fontanals, N., R. M. Marcé, and F. Borrull. "New hydrophilic materials for solid-phase extraction." TrAC Trends in Analytical Chemistry 24, no. 5 (May 2005): 394–406. http://dx.doi.org/10.1016/j.trac.2005.01.012.

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46

Qiao, Fengxia, Hanwen Sun, Hongyuan Yan, and Kyung Ho Row. "Molecularly Imprinted Polymers for Solid Phase Extraction." Chromatographia 64, no. 11-12 (November 17, 2006): 625–34. http://dx.doi.org/10.1365/s10337-006-0097-2.

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47

Medina, V. F., S. L. Larson, B. Extine, and A. Bednar. "Perchlorate Analysis Using Solid-Phase Extraction Cartridges." Journal of Chromatographic Science 43, no. 4 (April 1, 2005): 195–200. http://dx.doi.org/10.1093/chromsci/43.4.195.

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48

Płotka-Wasylka, Justyna, Mariusz Marć, Natalia Szczepańska, and Jacek Namieśnik. "New Polymeric Materials for Solid Phase Extraction." Critical Reviews in Analytical Chemistry 47, no. 5 (April 11, 2017): 373–83. http://dx.doi.org/10.1080/10408347.2017.1298987.

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49

Marcé, R. M., and F. Borrull. "Solid-phase extraction of polycyclic aromatic compounds." Journal of Chromatography A 885, no. 1-2 (July 2000): 273–90. http://dx.doi.org/10.1016/s0021-9673(00)00428-3.

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50

Fritz, James S., and Jeremy J. Masso. "Miniaturized solid-phase extraction with resin disks." Journal of Chromatography A 909, no. 1 (February 2001): 79–85. http://dx.doi.org/10.1016/s0021-9673(00)01014-1.

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